Chemistry Proceedings | An Open Access Journal from MDPI

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The conference organizers and proceedings editors are responsible for managing the peer review process and selecting papers for conference proceedings. </div> <div style="margin-bottom: 15px;"> </div> <div> <a href="/journal/chemproc/imprint" class="UI_JournalImprintsInfoButton"> <i class="material-icons spaced-link">subject</i> Imprint Information </a>    <a href="/journal/chemproc/chemproc_flyer.pdf" class="UD_JournalFlyer"> <i class="material-icons spaced-link">get_app</i> Journal Flyer </a>     <a class="oa-link" href="https://www.mdpi.com/about/openaccess"> <i class="material icons spaced-link"></i> Open Access </a>     <strong> ISSN: 2673-4583 </strong> </div> <div class="issue-cover"> <div style=" "> <a href=/2673-4583/14/1 > <img src="/files/uploaded/covers/chemproc/cover-chemproc-v14-i1.png " style="margin: 0px;" alt="Issue Cover" /> </a> </div> <h4>Vol. 14</h4> <h5>ECSOC 2023</h5> <div><a href=/2673-4583/14/1>Table of Contents</a></div> </div> <div class="issue-cover"> <div style=" "> <a href=/2673-4583/13/1 > <img src="/files/uploaded/covers/chemproc/cover-chemproc-v13-i1.png " style="margin: 0px;" alt="Issue Cover" /> </a> </div> <h4>Vol. 13</h4> <h5>Priochem 2023</h5> <div><a href=/2673-4583/13/1>Table of Contents</a></div> </div> <div class="issue-cover"> <div style=" "> <a href=/2673-4583/12/1 > <img src="/files/uploaded/covers/chemproc/cover-chemproc-v12-i1.png " style="margin: 0px;" alt="Issue Cover" /> </a> </div> <h4>Vol. 12</h4> <h5>ECSOC 2022</h5> <div><a href=/2673-4583/12/1>Table of Contents</a></div> </div> <div class="issue-cover"> <div style=" "> <a href=/2673-4583/11/1 > <img src="/files/uploaded/covers/chemproc/cover-chemproc-v11-i1.png " style="margin: 0px;" alt="Issue Cover" /> </a> </div> <h4>Vol. 11</h4> <h5>Stand Alone Papers 2022</h5> <div><a href=/2673-4583/11/1>Table of Contents</a></div> </div> <div class="issue-cover"> <div style=" "> <a href=/2673-4583/10/1 > <img src="/files/uploaded/covers/chemproc/cover-chemproc-v10-i1.png " style="margin: 0px;" alt="Issue Cover" /> </a> </div> <h4>Vol. 10</h4> <h5>IOCAG 2022</h5> <div><a href=/2673-4583/10/1>Table of Contents</a></div> </div> <div class="issue-cover"> <div style=" "> <a href=/2673-4583/9/1 > <img src="/files/uploaded/covers/chemproc/cover-chemproc-v9-i1.png " style="margin: 0px;" alt="Issue Cover" /> </a> </div> <h4>Vol. 9</h4> <h5>IOCC 2022</h5> <div><a href=/2673-4583/9/1>Table of Contents</a></div> </div> <div style="clear: both;"></div> </div> </div> </div> <div class="content__container content__container--overflow-initial"> <div class="custom-accordion-for-small-screen-link active"> <h2 class="no-padding-left">Latest Articles</h2> </div> <div class="custom-accordion-for-small-screen-content"> <div class="expanding-div collapsed"> <div class="generic-item article-item no-border"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 6 pages, 668 KiB   </span> <a href="/2673-4583/15/1/4/pdf?version=1732613812" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="Temperature Cycle-Induced Deracemization of Cl-TAK Using Amberlyst A26: A Heterogeneous Catalyst Approach for Efficient and Reusable Racemization" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/15/1/4">Temperature Cycle-Induced Deracemization of Cl-TAK Using Amberlyst A26: A Heterogeneous Catalyst Approach for Efficient and Reusable Racemization</a> <div class="authors"> by <span class="inlineblock "><strong>Jin Maeda</strong>, </span><span class="inlineblock "><strong>Pascal Cardinael</strong>, </span><span class="inlineblock "><strong>Gerard Coquerel</strong> and </span><span class="inlineblock "><strong>Adrian Flood</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2024</b>, <em>15</em>(1), 4; <a href="https://doi.org/10.3390/chemproc2024015004">https://doi.org/10.3390/chemproc2024015004</a> - 26 Nov 2024 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-cropped inline"> This study investigates the feasibility of employing Amberlyst A26 as a racemizing agent for the temperature cycle-induced deracemization (TCID) of the model compound Cl-TAK (1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl) pentan-3-one). We assessed Amberlyst A26 for its potential as a reusable heterogeneous catalyst, compatible with various solvents and <a href="#" data-counterslink = "https://www.mdpi.com/2673-4583/15/1/4/more" onclick="$(this).parents('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> [...] Read more.</a> </div> <div class="abstract-full "> This study investigates the feasibility of employing Amberlyst A26 as a racemizing agent for the temperature cycle-induced deracemization (TCID) of the model compound Cl-TAK (1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl) pentan-3-one). We assessed Amberlyst A26 for its potential as a reusable heterogeneous catalyst, compatible with various solvents and easily separable from the solution. Racemization rates at 20 °C and 25 °C confirmed its suitability, with experiments showing that Cl-TAK undergoes racemization only in the presence of the catalyst. TCID experiments with Amberlyst A26 yielded successful deracemization, achieving an 88% enantiomeric excess from an initial 30%. These findings highlight Amberlyst A26’s viability for industrial-scale TCID applications, emphasizing reusability and cost efficiency. <a href="/2673-4583/15/1/4">Full article</a> </div> </div> <a href="#" class="abstract-figures-show" data-counterslink = "https://www.mdpi.com/2673-4583/15/1/4/show" ><span >►</span><span style=" display: none;">▼</span> Show Figures </a><div class="abstract-image-preview "><div class="arrow left-arrow" id="prev1529646"><i class="fa fa-caret-left"></i></div><div class="arrow right-arrow" id="next1529646"><i class="fa fa-caret-right"></i></div><div class="absgraph cycle-slideshow manual" data-cycle-fx="scrollHorz" data-cycle-timeout="0" data-cycle-next="#next1529646" data-cycle-prev="#prev1529646" data-cycle-progressive="#images1529646" data-cycle-slides=">div" data-cycle-log="false"><div class='openpopupgallery cycle-slide' data-imgindex='0' data-target='article-1529646-popup'><span class="helper"></span><img src="data:image/gif;base64,R0lGODlhAQABAAD/ACwAAAAAAQABAAACADs=" data-src="https://pub.mdpi-res.com/chemproc/chemproc-15-00004/article_deploy/html/images/chemproc-15-00004-g001-550.jpg?1732613889" alt="" style="border: 0;"><p>Figure 1</p></div><script id="images1529646" type="text/cycle" data-cycle-split="---"><div class='openpopupgallery' data-imgindex='1' data-target='article-1529646-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-15-00004/article_deploy/html/images/chemproc-15-00004-g002-550.jpg?1732613890'><p>Figure 2</p></div></script></div></div><div id="article-1529646-popup" class="popupgallery" style="display: inline; line-height: 200%"><a href="https://pub.mdpi-res.com/chemproc/chemproc-15-00004/article_deploy/html/images/chemproc-15-00004-g001-550.jpg?1732613889" title=" <strong>Figure 1</strong><br/> <p>Racemization rates of Cl-TAK with Amberlyst A26 in 60 wt% methanol-water solution at 20 °C (<b>A</b>) and 25 °C (<b>B</b>).</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/15/1/4'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-15-00004/article_deploy/html/images/chemproc-15-00004-g002-550.jpg?1732613890" title=" <strong>Figure 2</strong><br/> <p>TCID experiment using Amberlyst A26. Evolution of c.e.e. of Cl-TAK over the number of temperature cycles.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/15/1/4'>Full article</a></strong> "></a></div> </div> </div> </div> <div class="extending-content content-ready"> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <a data-dropdown="drop-supplementary-1523133" aria-controls="drop-supplementary-1523133" aria-expanded="false" title="Supplementary Material"> <i class="material-icons">attachment</i> </a> <div id="drop-supplementary-1523133" class="f-dropdown label__btn__dropdown label__btn__dropdown--wide" data-dropdown-content aria-hidden="true" tabindex="-1"> Supplementary material: <br/> <a href="/2673-4583/15/1/3/s1?version=1731916370"> Supplementary File 1 (ZIP, 1543 KiB) </a><br/> </div> </div> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 9 pages, 5849 KiB   </span> <a href="/2673-4583/15/1/3/pdf?version=1731916369" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="Interfacial Action of Co-Doped MoS2 Nanosheets on Directional Piezoelectric Catalytic Generation of Reactive Oxygen Species" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/15/1/3">Interfacial Action of Co-Doped MoS<sub>2</sub> Nanosheets on Directional Piezoelectric Catalytic Generation of Reactive Oxygen Species</a> <div class="authors"> by <span class="inlineblock "><strong>Win Thi Yein</strong>, </span><span class="inlineblock "><strong>Dong-Su Kim</strong> and </span><span class="inlineblock "><strong>Qun Wang</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2024</b>, <em>15</em>(1), 3; <a href="https://doi.org/10.3390/chemproc2024015003">https://doi.org/10.3390/chemproc2024015003</a> - 18 Nov 2024 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-cropped inline"> Molybdenum disulfide (MoS<sub>2</sub>) with single- and odd-numbered layers is a novel piezocatalyst, and its piezocatalytic molecular oxygen activation is considered a promising and low-cost strategy for environmental remediation. In this study, the odd-numbered layers of Co-doped MoS<sub>2</sub> ultrathin nanosheets were <a href="#" data-counterslink = "https://www.mdpi.com/2673-4583/15/1/3/more" onclick="$(this).parents('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> [...] Read more.</a> </div> <div class="abstract-full "> Molybdenum disulfide (MoS<sub>2</sub>) with single- and odd-numbered layers is a novel piezocatalyst, and its piezocatalytic molecular oxygen activation is considered a promising and low-cost strategy for environmental remediation. In this study, the odd-numbered layers of Co-doped MoS<sub>2</sub> ultrathin nanosheets were successfully fabricated, which decomposed tetracycline by 99.8% in 15 min through shaking vibration. Moreover, to verify the enhanced piezoelectric catalytic activity of MoS<sub>2</sub> via the doping effect, molecular oxygen activation properties were predicted through DFT calculation and monitored by generated reactive oxygen species (ROS) evolution. In addition, the primary reactive species responsible for the degradation of tetracycline pollutants were also investigated in detail. <a href="/2673-4583/15/1/3">Full article</a> </div> </div> <a href="#" class="abstract-figures-show" data-counterslink = "https://www.mdpi.com/2673-4583/15/1/3/show" ><span >►</span><span style=" display: none;">▼</span> Show Figures </a><div class="abstract-image-preview "><div class="arrow left-arrow" id="prev1523133"><i class="fa fa-caret-left"></i></div><div class="arrow right-arrow" id="next1523133"><i class="fa fa-caret-right"></i></div><div class="absgraph cycle-slideshow manual" data-cycle-fx="scrollHorz" data-cycle-timeout="0" data-cycle-next="#next1523133" data-cycle-prev="#prev1523133" data-cycle-progressive="#images1523133" data-cycle-slides=">div" data-cycle-log="false"><div class='openpopupgallery cycle-slide' data-imgindex='0' data-target='article-1523133-popup'><span class="helper"></span><img src="data:image/gif;base64,R0lGODlhAQABAAD/ACwAAAAAAQABAAACADs=" data-src="https://pub.mdpi-res.com/chemproc/chemproc-15-00003/article_deploy/html/images/chemproc-15-00003-g001-550.jpg?1731916435" alt="" style="border: 0;"><p>Figure 1</p></div><script id="images1523133" type="text/cycle" data-cycle-split="---"><div class='openpopupgallery' data-imgindex='1' data-target='article-1523133-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-15-00003/article_deploy/html/images/chemproc-15-00003-g002-550.jpg?1731916438'><p>Figure 2</p></div> --- <div class='openpopupgallery' data-imgindex='2' data-target='article-1523133-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-15-00003/article_deploy/html/images/chemproc-15-00003-g003-550.jpg?1731916440'><p>Figure 3</p></div> --- <div class='openpopupgallery' data-imgindex='3' data-target='article-1523133-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-15-00003/article_deploy/html/images/chemproc-15-00003-g004-550.jpg?1731916441'><p>Figure 4</p></div></script></div></div><div id="article-1523133-popup" class="popupgallery" style="display: inline; line-height: 200%"><a href="https://pub.mdpi-res.com/chemproc/chemproc-15-00003/article_deploy/html/images/chemproc-15-00003-g001-550.jpg?1731916435" title=" <strong>Figure 1</strong><br/> <p>(<b>a</b>–<b>d</b>) SEM images, (<b>e</b>) XRD patterns of the MoS<sub>2</sub> and Co-doped MoS<sub>2</sub> samples, and (<b>f</b>) elemental mapping images of Co-MoS<sub>2</sub>-0.10; scale bar: 500 nm.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/15/1/3'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-15-00003/article_deploy/html/images/chemproc-15-00003-g002-550.jpg?1731916438" title=" <strong>Figure 2</strong><br/> <p>Co-MoS<sub>2</sub>-0.10. (<b>a</b>) TEM image, (<b>b</b>,<b>c</b>) front view and side view of HRTEM images, (<b>d</b>) AFM image, (<b>e</b>) Raman spectra, and (<b>f</b>) Mott–Schottky plot (inset: Mott–Schottky plot of bare MoS<sub>2</sub>).</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/15/1/3'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-15-00003/article_deploy/html/images/chemproc-15-00003-g003-550.jpg?1731916440" title=" <strong>Figure 3</strong><br/> <p>Degradation of tetracycline. (<b>a</b>) Piezocatalysis. (<b>b</b>) Bar plots represent the degradation kinetics of tetracycline in different Co-doped MoS<sub>2</sub> samples.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/15/1/3'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-15-00003/article_deploy/html/images/chemproc-15-00003-g004-550.jpg?1731916441" title=" <strong>Figure 4</strong><br/> <p>(<b>a</b>) DFT calculation: (i) perfect MoS<sub>2</sub> layer, (ii) Co-doped MoS<sub>2</sub> layer, and (iii) an adsorbed oxygen molecule at the Co dopant site in the lying-on configuration. (<b>b</b>) Working mechanism of piezocatalytic molecular oxygen activation reaction.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/15/1/3'>Full article</a></strong> "></a></div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 1 pages, 157 KiB   </span> <a href="/2673-4583/13/1/33/pdf?version=1731397241" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="Statement of Peer Review" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Editorial</span></div> <a class="title-link" href="/2673-4583/13/1/33">Statement of Peer Review</a> <div class="authors"> by <span class="inlineblock "><strong>Mihaela Doni</strong>, </span><span class="inlineblock "><strong>Florin Oancea</strong> and </span><span class="inlineblock "><strong>Radu Claudiu Fierăscu</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2023</b>, <em>13</em>(1), 33; <a href="https://doi.org/10.3390/chemproc2023013033">https://doi.org/10.3390/chemproc2023013033</a> - 12 Nov 2024 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-full inline"> In submitting conference proceedings to <i>Chemistry Proceedings</i>, the volume editors of the proceedings certify to the publisher that all papers published in this volume have been subjected to peer review administered by the volume editors [...] <a href="/2673-4583/13/1/33">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/13/1">Exploratory Workshop "Innovative Cross-Sectoral Technologies", Vth Edition, Secvent Project Meeting</a>)<br/> </div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 141 KiB   </span> <a href="/2673-4583/5/1/92/pdf?version=1713428760" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="Correction: Kumar et al. Numerical and Experimental Modeling of Paper-Based Actuators. Chem. Proc. 2021, 5, 15" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Correction</span></div> <a class="title-link" href="/2673-4583/5/1/92">Correction: Kumar et al. Numerical and Experimental Modeling of Paper-Based Actuators. <i>Chem. Proc.</i> 2021, <i>5</i>, 15</a> <div class="authors"> by <span class="inlineblock "><strong>Ashutosh Kumar</strong>, </span><span class="inlineblock "><strong>Hojat Heidari-Bafroui</strong>, </span><span class="inlineblock "><strong>Amer Charbaji</strong>, </span><span class="inlineblock "><strong>Nasim Rahmani</strong>, </span><span class="inlineblock "><strong>Constantine Anagnostopoulos</strong> and </span><span class="inlineblock "><strong>Mohammad Faghri</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2021</b>, <em>5</em>(1), 92; <a href="https://doi.org/10.3390/chemproc2021005092">https://doi.org/10.3390/chemproc2021005092</a> - 19 Mar 2024 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-full inline"> Text Correction [...] <a href="/2673-4583/5/1/92">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/5/1">The 1st International Electronic Conference on Chemical Sensors and Analytical Chemistry</a>)<br/> </div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 8 pages, 1670 KiB   </span> <a href="/2673-4583/13/1/32/pdf?version=1703219994" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="The Preparation and Characterization of Different Types of Eggshells Acidified with Acetic Acid" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/13/1/32">The Preparation and Characterization of Different Types of Eggshells Acidified with Acetic Acid</a> <div class="authors"> by <span class="inlineblock "><strong>Eliza-Gabriela Brettfeld</strong>, </span><span class="inlineblock "><strong>Daria-Gabriela Popa</strong>, </span><span class="inlineblock "><strong>Raluca Somoghi</strong>, </span><span class="inlineblock "><strong>Cristian Andi Nicolae</strong>, </span><span class="inlineblock "><strong>Adrian Birtas</strong>, </span><span class="inlineblock "><strong>Diana Constantinescu-Aruxandei</strong> and </span><span class="inlineblock "><strong>Florin Oancea</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2023</b>, <em>13</em>(1), 32; <a href="https://doi.org/10.3390/chemproc2023013032">https://doi.org/10.3390/chemproc2023013032</a> - 21 Dec 2023 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-cropped inline"> This paper investigates the acidification of eggshells of different origins with acetic acid. The acidification process was investigated for conventional and organic eggshells generated from the production of liquid eggs in the food industry and hatched eggshells from egg incubators. The acidified eggshell <a href="#" data-counterslink = "https://www.mdpi.com/2673-4583/13/1/32/more" onclick="$(this).parents('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> [...] Read more.</a> </div> <div class="abstract-full "> This paper investigates the acidification of eggshells of different origins with acetic acid. The acidification process was investigated for conventional and organic eggshells generated from the production of liquid eggs in the food industry and hatched eggshells from egg incubators. The acidified eggshell materials were characterized using Fourier-transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM) analysis, and thermogravimetric analysis (TGA). The results demonstrate that each type of investigated eggshell generates different nanostructures due to slight variations in their composition and this indicates potential applications: as a source of calcium supplements or to produce a snow-melting agent or CO<sub>2</sub> adsorbent. <a href="/2673-4583/13/1/32">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/13/1">Exploratory Workshop "Innovative Cross-Sectoral Technologies", Vth Edition, Secvent Project Meeting</a>)<br/> </div> <a href="#" class="abstract-figures-show" data-counterslink = "https://www.mdpi.com/2673-4583/13/1/32/show" ><span >►</span><span style=" display: none;">▼</span> Show Figures </a><div class="abstract-image-preview "><div class="arrow left-arrow" id="prev1305266"><i class="fa fa-caret-left"></i></div><div class="arrow right-arrow" id="next1305266"><i class="fa fa-caret-right"></i></div><div class="absgraph cycle-slideshow manual" data-cycle-fx="scrollHorz" data-cycle-timeout="0" data-cycle-next="#next1305266" data-cycle-prev="#prev1305266" data-cycle-progressive="#images1305266" data-cycle-slides=">div" data-cycle-log="false"><div class='openpopupgallery cycle-slide' data-imgindex='0' data-target='article-1305266-popup'><span class="helper"></span><img src="data:image/gif;base64,R0lGODlhAQABAAD/ACwAAAAAAQABAAACADs=" data-src="https://pub.mdpi-res.com/chemproc/chemproc-13-00032/article_deploy/html/images/chemproc-13-00032-g001-550.jpg?1703220070" alt="" style="border: 0;"><p>Figure 1</p></div><script id="images1305266" type="text/cycle" data-cycle-split="---"><div class='openpopupgallery' data-imgindex='1' data-target='article-1305266-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00032/article_deploy/html/images/chemproc-13-00032-g002-550.jpg?1703220073'><p>Figure 2</p></div> --- <div class='openpopupgallery' data-imgindex='2' data-target='article-1305266-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00032/article_deploy/html/images/chemproc-13-00032-g003-550.jpg?1703220073'><p>Figure 3</p></div></script></div></div><div id="article-1305266-popup" class="popupgallery" style="display: inline; line-height: 200%"><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00032/article_deploy/html/images/chemproc-13-00032-g001-550.jpg?1703220070" title=" <strong>Figure 1</strong><br/> <p>Transmission electron microscopy images of the acetic acid acidified eggshells. (<b>a</b>) Untreated conventional eggshells; (<b>b</b>) untreated organic eggshells; (<b>c</b>) untreated hatched eggshells; (<b>d</b>) conventional eggshells treated with acetic acid; (<b>e</b>) organic eggshells treated with acetic acid; (<b>f</b>) hatched eggshells treated with acetic acid.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/32'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00032/article_deploy/html/images/chemproc-13-00032-g002-550.jpg?1703220073" title=" <strong>Figure 2</strong><br/> <p>The FTIR spectra of the acidified and untreated samples compared with pure CaCO<sub>3</sub> and CaO. (<b>a</b>) Conventional eggshells; (<b>b</b>) organic eggshells; (<b>c</b>) hatched eggshells.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/32'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00032/article_deploy/html/images/chemproc-13-00032-g003-550.jpg?1703220073" title=" <strong>Figure 3</strong><br/> <p>The decomposition of calcium acetate derived from various assortments of eggshells, conventional/commercial, organic, and hatched.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/32'>Full article</a></strong> "></a></div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 7 pages, 1320 KiB   </span> <a href="/2673-4583/13/1/31/pdf?version=1703069647" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="Preparation of Ceramic Granules Enriched with Silicon Extracted from Reeds" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/13/1/31">Preparation of Ceramic Granules Enriched with Silicon Extracted from Reeds</a> <div class="authors"> by <span class="inlineblock "><strong>Mălina Deșliu-Avram</strong>, </span><span class="inlineblock "><strong>Luiza Capră</strong>, </span><span class="inlineblock "><strong>Ioana Tudor</strong>, </span><span class="inlineblock "><strong>Carmen Lupu</strong>, </span><span class="inlineblock "><strong>Diana Constantinescu-Aruxandei</strong>, </span><span class="inlineblock "><strong>Orsolya Csilla Raduly</strong>, </span><span class="inlineblock "><strong>Mariana Pătrașcu</strong> and </span><span class="inlineblock "><strong>Florin Oancea</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2023</b>, <em>13</em>(1), 31; <a href="https://doi.org/10.3390/chemproc2023013031">https://doi.org/10.3390/chemproc2023013031</a> - 20 Dec 2023 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-cropped inline"> This article presents the microwave-assisted extraction of biosilica from common reed (<i>Phragmites australis</i>) biomass and the utilization of the resulting aqueous extract to enrich porous ceramic granules based on diatomaceous earth and bentonite from white wine cleaning. The enriched porous ceramic <a href="#" data-counterslink = "https://www.mdpi.com/2673-4583/13/1/31/more" onclick="$(this).parents('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> [...] Read more.</a> </div> <div class="abstract-full "> This article presents the microwave-assisted extraction of biosilica from common reed (<i>Phragmites australis</i>) biomass and the utilization of the resulting aqueous extract to enrich porous ceramic granules based on diatomaceous earth and bentonite from white wine cleaning. The enriched porous ceramic granule generated a solution of soluble silicon that was +23.4 ± 2.2 more concentrated than the porous ceramic granules not enriched with reed extract. The water reactivity of Si-O-Si groups is higher in the polysilicic acid formed via the polycondensation of silicic acid extracted from reed, compared to the Si-O-Si group from diatomaceous earth or bentonite. <a href="/2673-4583/13/1/31">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/13/1">Exploratory Workshop "Innovative Cross-Sectoral Technologies", Vth Edition, Secvent Project Meeting</a>)<br/> </div> <a href="#" class="abstract-figures-show" data-counterslink = "https://www.mdpi.com/2673-4583/13/1/31/show" ><span >►</span><span style=" display: none;">▼</span> Show Figures </a><div class="abstract-image-preview "><div class="arrow left-arrow" id="prev1303950"><i class="fa fa-caret-left"></i></div><div class="arrow right-arrow" id="next1303950"><i class="fa fa-caret-right"></i></div><div class="absgraph cycle-slideshow manual" data-cycle-fx="scrollHorz" data-cycle-timeout="0" data-cycle-next="#next1303950" data-cycle-prev="#prev1303950" data-cycle-progressive="#images1303950" data-cycle-slides=">div" data-cycle-log="false"><div class='openpopupgallery cycle-slide' data-imgindex='0' data-target='article-1303950-popup'><span class="helper"></span><img src="data:image/gif;base64,R0lGODlhAQABAAD/ACwAAAAAAQABAAACADs=" data-src="https://pub.mdpi-res.com/chemproc/chemproc-13-00031/article_deploy/html/images/chemproc-13-00031-g001-550.jpg?1703069790" alt="" style="border: 0;"><p>Figure 1</p></div><script id="images1303950" type="text/cycle" data-cycle-split="---"><div class='openpopupgallery' data-imgindex='1' data-target='article-1303950-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00031/article_deploy/html/images/chemproc-13-00031-g002-550.jpg?1703069791'><p>Figure 2</p></div></script></div></div><div id="article-1303950-popup" class="popupgallery" style="display: inline; line-height: 200%"><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00031/article_deploy/html/images/chemproc-13-00031-g001-550.jpg?1703069790" title=" <strong>Figure 1</strong><br/> <p>The process for microwave-assisted extraction of silicon species from reed biomass.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/31'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00031/article_deploy/html/images/chemproc-13-00031-g002-550.jpg?1703069791" title=" <strong>Figure 2</strong><br/> <p>ATR-FT-IR spectra for: (<b>a</b>) diatomaceous earth (diatomite) and bentonite, and (<b>b</b>) amorphous silica resulting from extracted reed biomass.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/31'>Full article</a></strong> "></a></div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 9 pages, 2892 KiB   </span> <a href="/2673-4583/13/1/30/pdf?version=1703060622" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="Optimization of an Experimental Model for Microalgae Cultivation with CO2 Fixation" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/13/1/30">Optimization of an Experimental Model for Microalgae Cultivation with CO<sub>2</sub> Fixation</a> <div class="authors"> by <span class="inlineblock "><strong>Eliza-Gabriela Brettfeld</strong>, </span><span class="inlineblock "><strong>Daria-Gabriela Popa</strong>, </span><span class="inlineblock "><strong>Corina-Ioana Moga</strong>, </span><span class="inlineblock "><strong>Diana Constantinescu-Aruxandei</strong> and </span><span class="inlineblock "><strong>Florin Oancea</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2023</b>, <em>13</em>(1), 30; <a href="https://doi.org/10.3390/chemproc2023013030">https://doi.org/10.3390/chemproc2023013030</a> - 20 Dec 2023 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-cropped inline"> Microalgae cultivation is a promising approach for sustainable CO<sub>2</sub> fixation. This work describes the optimization of a laboratory-scale experimental model for microalgae cultivation under CO<sub>2</sub> supplementation. The experimental model was developed using a stirred clear glass reactor, white LED strips, connection <a href="#" data-counterslink = "https://www.mdpi.com/2673-4583/13/1/30/more" onclick="$(this).parents('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> [...] Read more.</a> </div> <div class="abstract-full "> Microalgae cultivation is a promising approach for sustainable CO<sub>2</sub> fixation. This work describes the optimization of a laboratory-scale experimental model for microalgae cultivation under CO<sub>2</sub> supplementation. The experimental model was developed using a stirred clear glass reactor, white LED strips, connection system caps with three ports, tubes, valves, regulators, and N<sub>2</sub>-CO<sub>2</sub> compressed gas cylinder. Three microalgae strains were used: <i>Raphidocelis subcapitata</i> ATCC22662, <i>Desmodesmus communis</i> NIVA-CHL 7, and <i>Chlorella sorokiniana</i> NIVA-CHL 176. The appropriate medium for cultivation of each of these strains was selected. The optimized experimental model demonstrated the positive influence of CO<sub>2</sub> supplementation on microalgae growth, particularly for <i>Chlorella sorokiniana</i>. <a href="/2673-4583/13/1/30">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/13/1">Exploratory Workshop "Innovative Cross-Sectoral Technologies", Vth Edition, Secvent Project Meeting</a>)<br/> </div> <a href="#" class="abstract-figures-show" data-counterslink = "https://www.mdpi.com/2673-4583/13/1/30/show" ><span >►</span><span style=" display: none;">▼</span> Show Figures </a><div class="abstract-image-preview "><div class="arrow left-arrow" id="prev1303735"><i class="fa fa-caret-left"></i></div><div class="arrow right-arrow" id="next1303735"><i class="fa fa-caret-right"></i></div><div class="absgraph cycle-slideshow manual" data-cycle-fx="scrollHorz" data-cycle-timeout="0" data-cycle-next="#next1303735" data-cycle-prev="#prev1303735" data-cycle-progressive="#images1303735" data-cycle-slides=">div" data-cycle-log="false"><div class='openpopupgallery cycle-slide' data-imgindex='0' data-target='article-1303735-popup'><span class="helper"></span><img src="data:image/gif;base64,R0lGODlhAQABAAD/ACwAAAAAAQABAAACADs=" data-src="https://pub.mdpi-res.com/chemproc/chemproc-13-00030/article_deploy/html/images/chemproc-13-00030-g001-550.jpg?1703060691" alt="" style="border: 0;"><p>Figure 1</p></div><script id="images1303735" type="text/cycle" data-cycle-split="---"><div class='openpopupgallery' data-imgindex='1' data-target='article-1303735-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00030/article_deploy/html/images/chemproc-13-00030-g002-550.jpg?1703060691'><p>Figure 2</p></div> --- <div class='openpopupgallery' data-imgindex='2' data-target='article-1303735-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00030/article_deploy/html/images/chemproc-13-00030-g003-550.jpg?1703060692'><p>Figure 3</p></div> --- <div class='openpopupgallery' data-imgindex='3' data-target='article-1303735-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00030/article_deploy/html/images/chemproc-13-00030-g004-550.jpg?1703060693'><p>Figure 4</p></div> --- <div class='openpopupgallery' data-imgindex='4' data-target='article-1303735-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00030/article_deploy/html/images/chemproc-13-00030-g005-550.jpg?1703060693'><p>Figure 5</p></div> --- <div class='openpopupgallery' data-imgindex='5' data-target='article-1303735-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00030/article_deploy/html/images/chemproc-13-00030-g006-550.jpg?1703060694'><p>Figure 6</p></div></script></div></div><div id="article-1303735-popup" class="popupgallery" style="display: inline; line-height: 200%"><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00030/article_deploy/html/images/chemproc-13-00030-g001-550.jpg?1703060691" title=" <strong>Figure 1</strong><br/> <p>The experimental setup for screening the development of microalgae for CO<sub>2</sub> fixation.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/30'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00030/article_deploy/html/images/chemproc-13-00030-g002-550.jpg?1703060691" title=" <strong>Figure 2</strong><br/> <p>Optical densities for the three microalgae strains in the three cultivation media. The bars height are mean values ± statistical error bars. For the values with the same letter the difference between the means is not statistically significant at <span class="html-italic">p</span> &lt; 0.05.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/30'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00030/article_deploy/html/images/chemproc-13-00030-g003-550.jpg?1703060692" title=" <strong>Figure 3</strong><br/> <p>Turbidity (McFarland) for the three microalgae strains in the three cultivation media. The bars height are mean values ± statistical error bars. For the values with the same letter the difference between the means is not statistically significant at <span class="html-italic">p</span> &lt; 0.05.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/30'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00030/article_deploy/html/images/chemproc-13-00030-g004-550.jpg?1703060693" title=" <strong>Figure 4</strong><br/> <p>Biomass accumulation of each microalgae strain in different media after 15 days of cultivation. The bars height are mean values ± statistical error bars. For the values with the same letter the difference between the means is not statistically significant at <span class="html-italic">p</span> &lt; 0.05.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/30'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00030/article_deploy/html/images/chemproc-13-00030-g005-550.jpg?1703060693" title=" <strong>Figure 5</strong><br/> <p>Optical density for microalgae growth with and without CO<sub>2</sub> supplementation. (<b>Left</b>) <span class="html-italic">Chlorella sorokiniana</span>. (<b>Right</b>) <span class="html-italic">Desmodesmus communis</span>. The bars height are mean values ± statistical error bars. For the values with the same letter the difference between the means is not statistically significant at <span class="html-italic">p</span>&lt;0.05.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/30'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00030/article_deploy/html/images/chemproc-13-00030-g006-550.jpg?1703060694" title=" <strong>Figure 6</strong><br/> <p>Cell number for microalgae growth using CO<sub>2</sub>. (<b>Left</b>) <span class="html-italic">Chlorella sorokiniana</span> (Ch. sk.). (<b>Right</b>) <span class="html-italic">Desmodesmus communis</span> (Dmd). The bars height are mean values ± statistical error bars. For the values with the same letter the difference between the means is not statistically significant at <span class="html-italic">p</span>&lt;0.05.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/30'>Full article</a></strong> "></a></div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 7 pages, 2057 KiB   </span> <a href="/2673-4583/13/1/29/pdf?version=1703055576" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="Bioaugmentation Performance of a Bacterial Consortium for Moving Bed Biofilm Reactor (MBBR) Treating Municipal Wastewater" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/13/1/29">Bioaugmentation Performance of a Bacterial Consortium for Moving Bed Biofilm Reactor (MBBR) Treating Municipal Wastewater</a> <div class="authors"> by <span class="inlineblock "><strong>Eliza-Gabriela Brettfeld</strong>, </span><span class="inlineblock "><strong>Oana-Andreea Cheoafa</strong>, </span><span class="inlineblock "><strong>Diana Constantinescu-Aruxandei</strong> and </span><span class="inlineblock "><strong>Florin Oancea</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2023</b>, <em>13</em>(1), 29; <a href="https://doi.org/10.3390/chemproc2023013029">https://doi.org/10.3390/chemproc2023013029</a> - 20 Dec 2023 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-cropped inline"> A compatible microbial consortium with a high organic pollutant degradation ability, which includes a gram-positive <i>Brevibacillus parabrevis</i> B50 NCAIM B 001413 bacterial strain and a gram-negative <i>Pseudoxanthomonas mexicana</i> P32 NCAIM (P) B 001414 bacterial strain, was selected using high-throughput screening techniques. The compatible <a href="#" data-counterslink = "https://www.mdpi.com/2673-4583/13/1/29/more" onclick="$(this).parents('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> [...] Read more.</a> </div> <div class="abstract-full "> A compatible microbial consortium with a high organic pollutant degradation ability, which includes a gram-positive <i>Brevibacillus parabrevis</i> B50 NCAIM B 001413 bacterial strain and a gram-negative <i>Pseudoxanthomonas mexicana</i> P32 NCAIM (P) B 001414 bacterial strain, was selected using high-throughput screening techniques. The compatible microbial consortium, encapsulated in alginate beds, was used to inoculate moving bed biofilm reactors from a small municipal wastewater treatment plant. The bioaugmentation performance of the inoculated consortium was evaluated by determining the water quality parameters before inoculation and one month after bioaugmentation treatment. The removal of organic matter was enhanced after treatment with the selected microbial consortium. <a href="/2673-4583/13/1/29">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/13/1">Exploratory Workshop "Innovative Cross-Sectoral Technologies", Vth Edition, Secvent Project Meeting</a>)<br/> </div> <a href="#" class="abstract-figures-show" data-counterslink = "https://www.mdpi.com/2673-4583/13/1/29/show" ><span >►</span><span style=" display: none;">▼</span> Show Figures </a><div class="abstract-image-preview "><div class="arrow left-arrow" id="prev1303650"><i class="fa fa-caret-left"></i></div><div class="arrow right-arrow" id="next1303650"><i class="fa fa-caret-right"></i></div><div class="absgraph cycle-slideshow manual" data-cycle-fx="scrollHorz" data-cycle-timeout="0" data-cycle-next="#next1303650" data-cycle-prev="#prev1303650" data-cycle-progressive="#images1303650" data-cycle-slides=">div" data-cycle-log="false"><div class='openpopupgallery cycle-slide' data-imgindex='0' data-target='article-1303650-popup'><span class="helper"></span><img src="data:image/gif;base64,R0lGODlhAQABAAD/ACwAAAAAAQABAAACADs=" data-src="https://pub.mdpi-res.com/chemproc/chemproc-13-00029/article_deploy/html/images/chemproc-13-00029-g001-550.jpg?1703055674" alt="" style="border: 0;"><p>Figure 1</p></div><script id="images1303650" type="text/cycle" data-cycle-split="---"><div class='openpopupgallery' data-imgindex='1' data-target='article-1303650-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00029/article_deploy/html/images/chemproc-13-00029-g002-550.jpg?1703055675'><p>Figure 2</p></div> --- <div class='openpopupgallery' data-imgindex='2' data-target='article-1303650-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00029/article_deploy/html/images/chemproc-13-00029-g003-550.jpg?1703055676'><p>Figure 3</p></div> --- <div class='openpopupgallery' data-imgindex='3' data-target='article-1303650-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00029/article_deploy/html/images/chemproc-13-00029-g004-550.jpg?1703055676'><p>Figure 4</p></div></script></div></div><div id="article-1303650-popup" class="popupgallery" style="display: inline; line-height: 200%"><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00029/article_deploy/html/images/chemproc-13-00029-g001-550.jpg?1703055674" title=" <strong>Figure 1</strong><br/> <p>pH (<b>a</b>), electrical conductivity (<b>b</b>), and chloride values (<b>c</b>), determined for initial samples from untreated water, samples after bioaugmentation treatment, and maximum threshold values.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/29'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00029/article_deploy/html/images/chemproc-13-00029-g002-550.jpg?1703055675" title=" <strong>Figure 2</strong><br/> <p>Chemical oxygen demand (COD, <b>a</b>), biochemical oxygen demand (BOD5, <b>b</b>), total suspended solid (<b>c</b>), determined for initial samples from untreated water, samples after bioaugmentation treatment, and maximum threshold values.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/29'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00029/article_deploy/html/images/chemproc-13-00029-g003-550.jpg?1703055676" title=" <strong>Figure 3</strong><br/> <p>Residues at 105 °C (<b>a</b>), extractible organic substances (<b>b</b>), total nitrogen (<b>c</b>), determined for initial samples from untreated water, samples after bioaugmentation treatment, and maximum threshold values.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/29'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00029/article_deploy/html/images/chemproc-13-00029-g004-550.jpg?1703055676" title=" <strong>Figure 4</strong><br/> <p>Biodegradable synthetic detergents (<b>a</b>), and total phosphorus (<b>b</b>), determined for initial samples from untreated water, samples after bioaugmentation treatment, and maximum threshold values.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/29'>Full article</a></strong> "></a></div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 6 pages, 781 KiB   </span> <a href="/2673-4583/13/1/28/pdf?version=1703065650" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="Preparation of a Veterinary Supplement That Reduces Aflatoxin B1 Availability" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/13/1/28">Preparation of a Veterinary Supplement That Reduces Aflatoxin B<sub>1</sub> Availability</a> <div class="authors"> by <span class="inlineblock "><strong>Mălina Deșliu-Avram</strong>, </span><span class="inlineblock "><strong>Carmen Lupu</strong>, </span><span class="inlineblock "><strong>Simona Rotaru</strong>, </span><span class="inlineblock "><strong>Diana Constantinescu-Aruxandei</strong>, </span><span class="inlineblock "><strong>Radian Nicolae Negrilă</strong> and </span><span class="inlineblock "><strong>Florin Oancea</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2023</b>, <em>13</em>(1), 28; <a href="https://doi.org/10.3390/chemproc2023013028">https://doi.org/10.3390/chemproc2023013028</a> - 20 Dec 2023 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-cropped inline"> This work describes the preparation of a veterinary supplement based on diatomaceous earth, chemically hydrolyzed proteins, and essential oils, which are applicable for protecting monogastric animals against the mycotoxin contamination of cereal-based feeds. The veterinary supplement comprises 54.5–55% diatomaceous earth, 40.5–41% hydrolyzed proteins <a href="#" data-counterslink = "https://www.mdpi.com/2673-4583/13/1/28/more" onclick="$(this).parents('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> [...] Read more.</a> </div> <div class="abstract-full "> This work describes the preparation of a veterinary supplement based on diatomaceous earth, chemically hydrolyzed proteins, and essential oils, which are applicable for protecting monogastric animals against the mycotoxin contamination of cereal-based feeds. The veterinary supplement comprises 54.5–55% diatomaceous earth, 40.5–41% hydrolyzed proteins (whey protein concentrate and soybean protein isolate), 2.4–2.5% oregano essential oils, 0.6–0.7% NaCl, and 1.6% CaCl<sub>2</sub>. The preparation process includes alkaline thermal hydrolysis of proteins, followed by emulsification of the essential oil with protein hydrolysate and granulation with diatomaceous earth. The veterinary supplement prepared in this work reduces the availability of aflatoxin B<sub>1</sub> in a simulated gastric fluid by 82.7 ± 4.43%. <a href="/2673-4583/13/1/28">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/13/1">Exploratory Workshop "Innovative Cross-Sectoral Technologies", Vth Edition, Secvent Project Meeting</a>)<br/> </div> <a href="#" class="abstract-figures-show" data-counterslink = "https://www.mdpi.com/2673-4583/13/1/28/show" ><span >►</span><span style=" display: none;">▼</span> Show Figures </a><div class="abstract-image-preview "><div class="arrow left-arrow" id="prev1303842"><i class="fa fa-caret-left"></i></div><div class="arrow right-arrow" id="next1303842"><i class="fa fa-caret-right"></i></div><div class="absgraph cycle-slideshow manual" data-cycle-fx="scrollHorz" data-cycle-timeout="0" data-cycle-next="#next1303842" data-cycle-prev="#prev1303842" data-cycle-progressive="#images1303842" data-cycle-slides=">div" data-cycle-log="false"><div class='openpopupgallery cycle-slide' data-imgindex='0' data-target='article-1303842-popup'><span class="helper"></span><img src="data:image/gif;base64,R0lGODlhAQABAAD/ACwAAAAAAQABAAACADs=" data-src="https://pub.mdpi-res.com/chemproc/chemproc-13-00028/article_deploy/html/images/chemproc-13-00028-g001-550.jpg?1703065722" alt="" style="border: 0;"><p>Figure 1</p></div><script id="images1303842" type="text/cycle" data-cycle-split="---"><div class='openpopupgallery' data-imgindex='1' data-target='article-1303842-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00028/article_deploy/html/images/chemproc-13-00028-g002-550.jpg?1703065723'><p>Figure 2</p></div> --- <div class='openpopupgallery' data-imgindex='2' data-target='article-1303842-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00028/article_deploy/html/images/chemproc-13-00028-g003-550.jpg?1703065724'><p>Figure 3</p></div></script></div></div><div id="article-1303842-popup" class="popupgallery" style="display: inline; line-height: 200%"><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00028/article_deploy/html/images/chemproc-13-00028-g001-550.jpg?1703065722" title=" <strong>Figure 1</strong><br/> <p>Illustration of the process for the preparation of the veterinary supplement.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/28'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00028/article_deploy/html/images/chemproc-13-00028-g002-550.jpg?1703065723" title=" <strong>Figure 2</strong><br/> <p>Preparation of essential oil emulsified with protein hydrolysate (<b>a</b>) and pan granulation (<b>b</b>) of the veterinary supplement.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/28'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00028/article_deploy/html/images/chemproc-13-00028-g003-550.jpg?1703065724" title=" <strong>Figure 3</strong><br/> <p>Chromatogram of the veterinary supplement sample.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/28'>Full article</a></strong> "></a></div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 7 pages, 3851 KiB   </span> <a href="/2673-4583/14/1/54/pdf?version=1702613028" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="99mTc-Selenium-NPs as SPECT Tracers: Radio Synthesis and Biological Evaluation" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/14/1/54"><sup>99m</sup>Tc-Selenium-NPs as SPECT Tracers: Radio Synthesis and Biological Evaluation</a> <div class="authors"> by <span class="inlineblock "><strong>Akhilesh Kumar Singh</strong>, </span><span class="inlineblock "><strong>Mohd. Faheem</strong>, </span><span class="inlineblock "><strong>Amit Jaiswal</strong>, </span><span class="inlineblock "><strong>Malleswari Ponnala</strong>, </span><span class="inlineblock "><strong>Sanjay Gambhir</strong> and </span><span class="inlineblock "><strong>Manish Dixit</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2023</b>, <em>14</em>(1), 54; <a href="https://doi.org/10.3390/ecsoc-27-16172">https://doi.org/10.3390/ecsoc-27-16172</a> - 14 Dec 2023 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-cropped inline"> As the usage of nano-sized complexes in biomedical applications has grown significantly over the past ten years, nanoparticles are now playing a significant role in the enhancement and revolution of medical applications. It may be due primarily to the novel and exceptional electrical, <a href="#" data-counterslink = "https://www.mdpi.com/2673-4583/14/1/54/more" onclick="$(this).parents('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> [...] Read more.</a> </div> <div class="abstract-full "> As the usage of nano-sized complexes in biomedical applications has grown significantly over the past ten years, nanoparticles are now playing a significant role in the enhancement and revolution of medical applications. It may be due primarily to the novel and exceptional electrical, optical, photo-responsive, and catalytic capabilities displayed by particles with sizes ranging from 1 to 100 nm. The radiolabelled nanoparticles refer to the process of incorporating radioactive isotopes into nanoparticles. This technique enables the nanoparticles to be tracked, imaged and monitored using various imaging techniques, such as Single-Photon Emission Computed Tomography (SPECT/CT) or Positron Emission Tomography (PET). They play a crucial role in understanding the biodistribution, pharmacokinetics, and targeted delivery of nanoparticles to biological systems. In this study, selenium-based nanoparticles (Se-NPs) were explored for imaging potential as these are usable due to their size, surface, and kinetics, as well as their ability to be functionalised. The <sup>99m</sup>Technicium (<sup>99m</sup>Tc) radionuclide was used to radiolabel the bio-inspired highly dispersed over grown endophytic fungus <i>Fusarium oxysporum</i> selenium NP using conventional radiochemistry protocol. The radiolabelling yield was found to be 94.5 ± 3% and analysed by various analytical tools. The synthesized <sup>99m</sup>Tc-Se-NPs were assessed through <i>In-vitro</i> stability, and their <i>In-vivo</i> biodistribution was performed. The accumulation of post six-hour data was primarily seen in the liver (around 3.4% ID/g) and lungs (about 2.2% ID/g). These Se-NPs can be used as an imaging agent for lung and liver disorders because these NPs quickly pass through the kidneys are expelled via urine and show a long retention time in the body. These properties of <sup>99m</sup>Tc-Se-NPs can be used for non-invasive imaging via SPECT. <a href="/2673-4583/14/1/54">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/14/1">27th International Electronic Conference on Synthetic Organic Chemistry</a>)<br/> </div> <a href="#" class="abstract-figures-show" data-counterslink = "https://www.mdpi.com/2673-4583/14/1/54/show" ><span >►</span><span style=" display: none;">▼</span> Show Figures </a><div class="abstract-image-preview "><div class="arrow left-arrow" id="prev1300535"><i class="fa fa-caret-left"></i></div><div class="arrow right-arrow" id="next1300535"><i class="fa fa-caret-right"></i></div><div class="absgraph cycle-slideshow manual" data-cycle-fx="scrollHorz" data-cycle-timeout="0" data-cycle-next="#next1300535" data-cycle-prev="#prev1300535" data-cycle-progressive="#images1300535" data-cycle-slides=">div" data-cycle-log="false"><div class='openpopupgallery cycle-slide' data-imgindex='0' data-target='article-1300535-popup'><span class="helper"></span><img src="data:image/gif;base64,R0lGODlhAQABAAD/ACwAAAAAAQABAAACADs=" data-src="https://pub.mdpi-res.com/chemproc/chemproc-14-00054/article_deploy/html/images/chemproc-14-00054-g001-550.jpg?1702613120" alt="" style="border: 0;"><p>Figure 1</p></div><script id="images1300535" type="text/cycle" data-cycle-split="---"><div class='openpopupgallery' data-imgindex='1' data-target='article-1300535-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00054/article_deploy/html/images/chemproc-14-00054-g002-550.jpg?1702613122'><p>Figure 2</p></div> --- <div class='openpopupgallery' data-imgindex='2' data-target='article-1300535-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00054/article_deploy/html/images/chemproc-14-00054-g003-550.jpg?1702613124'><p>Figure 3</p></div> --- <div class='openpopupgallery' data-imgindex='3' data-target='article-1300535-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00054/article_deploy/html/images/chemproc-14-00054-g004-550.jpg?1702613125'><p>Figure 4</p></div></script></div></div><div id="article-1300535-popup" class="popupgallery" style="display: inline; line-height: 200%"><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00054/article_deploy/html/images/chemproc-14-00054-g001-550.jpg?1702613120" title=" <strong>Figure 1</strong><br/> <p>Systematic synthesis of radiolabelled Se-NPs with <sup>99m</sup>Tc radionuclide.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/54'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00054/article_deploy/html/images/chemproc-14-00054-g002-550.jpg?1702613122" title=" <strong>Figure 2</strong><br/> <p>Stability study of [<sup>99m</sup>Tc]TcSe-NPs at different time intervals (<b>a</b>) in saline and (<b>b</b>) in albumin at 37 °C.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/54'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00054/article_deploy/html/images/chemproc-14-00054-g003-550.jpg?1702613124" title=" <strong>Figure 3</strong><br/> <p>SPECT-based imaging of [<sup>99m</sup>Tc]TcSe-NPs in Wister rats.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/54'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00054/article_deploy/html/images/chemproc-14-00054-g004-550.jpg?1702613125" title=" <strong>Figure 4</strong><br/> <p>Biodistribution of [<sup>99m</sup>Tc]TcSe-NPs in Wister rat organs.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/54'>Full article</a></strong> "></a></div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 3 pages, 533 KiB   </span> <a href="/2673-4583/14/1/8/pdf?version=1701930082" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="The Reaction of 1,6-Diamino-4-aryl-2-oxo-1,2-dihydropyridine- 3,5-Dicarbonitriles with Certain Electrophilic Agents" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/14/1/8">The Reaction of 1,6-Diamino-4-aryl-2-oxo-1,2-dihydropyridine- 3,5-Dicarbonitriles with Certain Electrophilic Agents</a> <div class="authors"> by <span class="inlineblock "><strong>Alexei A. Dolganov</strong>, </span><span class="inlineblock "><strong>Alexandra R. Chikava</strong> and </span><span class="inlineblock "><strong>Victor V. Dotsenko</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2023</b>, <em>14</em>(1), 8; <a href="https://doi.org/10.3390/ecsoc-27-16081">https://doi.org/10.3390/ecsoc-27-16081</a> - 6 Dec 2023 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-full inline"> The reaction of 1,6-diamino-2-oxo-1,2-dihydropyridine-3,5-dicarbonitriles, which are easily available through the reaction of cyanoacetohydrazide with arylmethylene malononitriles, with ninhydrin leads to the formation of novel dihydroindeno[1,2-e]pyrido[1,2-b][1,2,4]triazines. Another active carbonyl compound, glyoxal, reacts with 1,6-diamino-2-oxo-1,2-dihydropyridine-3,5-dicarbonitriles under mild conditions to give functionalized 6-oxo-6H-pyrido[1,2-b][1,2,4]triazine-7,9-dicarbonitriles. <a href="/2673-4583/14/1/8">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/14/1">27th International Electronic Conference on Synthetic Organic Chemistry</a>)<br/> </div> <a href="#" class="abstract-figures-show" data-counterslink = "https://www.mdpi.com/2673-4583/14/1/8/show" ><span >►</span><span style=" display: none;">▼</span> Show Figures </a><div class="abstract-image-preview "><div class="arrow left-arrow" id="prev1295235"><i class="fa fa-caret-left"></i></div><div class="arrow right-arrow" id="next1295235"><i class="fa fa-caret-right"></i></div><div class="absgraph cycle-slideshow manual" data-cycle-fx="scrollHorz" data-cycle-timeout="0" data-cycle-next="#next1295235" data-cycle-prev="#prev1295235" data-cycle-progressive="#images1295235" data-cycle-slides=">div" data-cycle-log="false"><div class='openpopupgallery cycle-slide' data-imgindex='0' data-target='article-1295235-popup'><span class="helper"></span><img src="data:image/gif;base64,R0lGODlhAQABAAD/ACwAAAAAAQABAAACADs=" data-src="https://pub.mdpi-res.com/chemproc/chemproc-14-00008/article_deploy/html/images/chemproc-14-00008-sch001-550.jpg?1701930149" alt="" style="border: 0;"><p>Scheme 1</p></div><script id="images1295235" type="text/cycle" data-cycle-split="---"><div class='openpopupgallery' data-imgindex='1' data-target='article-1295235-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00008/article_deploy/html/images/chemproc-14-00008-sch002-550.jpg?1701930150'><p>Scheme 2</p></div> --- <div class='openpopupgallery' data-imgindex='2' data-target='article-1295235-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00008/article_deploy/html/images/chemproc-14-00008-sch003-550.jpg?1701930151'><p>Scheme 3</p></div></script></div></div><div id="article-1295235-popup" class="popupgallery" style="display: inline; line-height: 200%"><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00008/article_deploy/html/images/chemproc-14-00008-sch001-550.jpg?1701930149" title=" <strong>Scheme 1</strong><br/> <p>Preparation of 1,6-diamino-2-oxo-1,2-dihydropyridine-3,5-dicarbonitriles <b>1</b>.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/8'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00008/article_deploy/html/images/chemproc-14-00008-sch002-550.jpg?1701930150" title=" <strong>Scheme 2</strong><br/> <p>The preparation of dihydroindeno[1,2-e]pyrido[1,2-b][1,2,4]triazines <b>5</b>.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/8'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00008/article_deploy/html/images/chemproc-14-00008-sch003-550.jpg?1701930151" title=" <strong>Scheme 3</strong><br/> <p>The preparation of pyrido[1,2-b][1,2,4]triazines <b>7</b> (R = Hal, MeO).</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/8'>Full article</a></strong> "></a></div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 764 KiB   </span> <a href="/2673-4583/14/1/100/pdf?version=1706589948" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="In Vitro and In Silico Antioxidant Activity of Hydrazones and Semicarbazones Derived from Aldehydes Found in Essential Oils" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/14/1/100"><i>In Vitro</i> and <i>In Silico</i> Antioxidant Activity of Hydrazones and Semicarbazones Derived from Aldehydes Found in Essential Oils</a> <div class="authors"> by <span class="inlineblock "><strong>Leandro G. Gutierrez</strong>, </span><span class="inlineblock "><strong>Carla M. Ormachea</strong>, </span><span class="inlineblock "><strong>Ana P. Reinick</strong>, </span><span class="inlineblock "><strong>Vanina A. Guntero</strong> and </span><span class="inlineblock "><strong>Cristián A. Ferretti</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2023</b>, <em>14</em>(1), 100; <a href="https://doi.org/10.3390/ecsoc-27-16577">https://doi.org/10.3390/ecsoc-27-16577</a> - 4 Dec 2023 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-cropped inline"> The aim of this study was to investigate the <i>in vitro</i> and <i>in silico</i> antioxidant properties of four hydrazones and semicarbazones derived from vanillin and cinnamaldehyde, aromatic aldehydes found in essential oils. They were synthesized by condensation of these aldehydes with the corresponding <a href="#" data-counterslink = "https://www.mdpi.com/2673-4583/14/1/100/more" onclick="$(this).parents('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> [...] Read more.</a> </div> <div class="abstract-full "> The aim of this study was to investigate the <i>in vitro</i> and <i>in silico</i> antioxidant properties of four hydrazones and semicarbazones derived from vanillin and cinnamaldehyde, aromatic aldehydes found in essential oils. They were synthesized by condensation of these aldehydes with the corresponding phenylhydrazine and semicarbazide in good yields. The antioxidant properties of the target molecules were determined using the Reducing Power assay (RP) and the hydrogen peroxide scavenging method (HP), and the results were compared with thermodynamic descriptors obtained from theoretical calculations using the DFT method. The target molecules were shown to be highly active for the total antioxidant assay and the results of theoretical calculations were consistent with the antioxidant activity observed experimentally, making them a useful tool to understand the mechanism of action. This would also allow theoretical tests of new antioxidant compounds to be carried out in a predictive manner. <a href="/2673-4583/14/1/100">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/14/1">27th International Electronic Conference on Synthetic Organic Chemistry</a>)<br/> </div> <a href="#" class="abstract-figures-show" data-counterslink = "https://www.mdpi.com/2673-4583/14/1/100/show" ><span >►</span><span style=" display: none;">▼</span> Show Figures </a><div class="abstract-image-preview "><div class="arrow left-arrow" id="prev1329216"><i class="fa fa-caret-left"></i></div><div class="arrow right-arrow" id="next1329216"><i class="fa fa-caret-right"></i></div><div class="absgraph cycle-slideshow manual" data-cycle-fx="scrollHorz" data-cycle-timeout="0" data-cycle-next="#next1329216" data-cycle-prev="#prev1329216" data-cycle-progressive="#images1329216" data-cycle-slides=">div" data-cycle-log="false"><div class='openpopupgallery cycle-slide' data-imgindex='0' data-target='article-1329216-popup'><span class="helper"></span><img src="data:image/gif;base64,R0lGODlhAQABAAD/ACwAAAAAAQABAAACADs=" data-src="https://pub.mdpi-res.com/chemproc/chemproc-14-00100/article_deploy/html/images/chemproc-14-00100-g001-550.jpg?1706590016" alt="" style="border: 0;"><p>Figure 1</p></div><script id="images1329216" type="text/cycle" data-cycle-split="---"><div class='openpopupgallery' data-imgindex='1' data-target='article-1329216-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00100/article_deploy/html/images/chemproc-14-00100-g002-550.jpg?1706590018'><p>Figure 2</p></div> --- <div class='openpopupgallery' data-imgindex='2' data-target='article-1329216-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00100/article_deploy/html/images/chemproc-14-00100-sch001-550.jpg?1706590019'><p>Scheme 1</p></div></script></div></div><div id="article-1329216-popup" class="popupgallery" style="display: inline; line-height: 200%"><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00100/article_deploy/html/images/chemproc-14-00100-g001-550.jpg?1706590016" title=" <strong>Figure 1</strong><br/> <p>(<b>a</b>) Dependence of the reducing power as a function of time for the target compounds; (<b>b</b>) increase in absorbance at 700 nm for the targeted molecules after 240 min.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/100'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00100/article_deploy/html/images/chemproc-14-00100-g002-550.jpg?1706590018" title=" <strong>Figure 2</strong><br/> <p>Percentage of H<sub>2</sub>O<sub>2</sub> scavenged for the target compounds <b>1a–b</b> and <b>2a–b</b> at different concentrations (20–80 µg/mL).</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/100'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00100/article_deploy/html/images/chemproc-14-00100-sch001-550.jpg?1706590019" title=" <strong>Scheme 1</strong><br/> <p>Hydrazones and semicarbazones obtained from vanillin (<b>1a</b>–<b>b</b>) and cinnamaldehyde (<b>2a</b>–<b>b</b>).</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/100'>Full article</a></strong> "></a></div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 1442 KiB   </span> <a href="/2673-4583/14/1/87/pdf?version=1705022384" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="Selective Synthesis of Fatty Alcohols over Mild Reaction Conditions via Non-Catalytic Liquid-Phase Fatty Acid Methyl Esters’ Reduction" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/14/1/87">Selective Synthesis of Fatty Alcohols over Mild Reaction Conditions via Non-Catalytic Liquid-Phase Fatty Acid Methyl Esters’ Reduction</a> <div class="authors"> by <span class="inlineblock "><strong>Alejandro Vallejo Orrego</strong>, </span><span class="inlineblock "><strong>Cristián A. Ferretti</strong> and </span><span class="inlineblock "><strong>Verónica K. Díez</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2023</b>, <em>14</em>(1), 87; <a href="https://doi.org/10.3390/ecsoc-27-16384">https://doi.org/10.3390/ecsoc-27-16384</a> - 30 Nov 2023 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-cropped inline"> The upgrading of fatty alcohols synthesis from natural fatty acid methyl esters’ reduction using alumina-supported NaBH<sub>4</sub> without H<sub>2</sub> supply was investigated. It was possible to synthesize fatty alcohols efficiently with high yields. By using pure NaBH<sub>4</sub> or alumina-supported NaBH<sub>4</sub> <a href="#" data-counterslink = "https://www.mdpi.com/2673-4583/14/1/87/more" onclick="$(this).parents('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> [...] Read more.</a> </div> <div class="abstract-full "> The upgrading of fatty alcohols synthesis from natural fatty acid methyl esters’ reduction using alumina-supported NaBH<sub>4</sub> without H<sub>2</sub> supply was investigated. It was possible to synthesize fatty alcohols efficiently with high yields. By using pure NaBH<sub>4</sub> or alumina-supported NaBH<sub>4</sub> and methanol as co-reactants, 100% selectivity towards fatty alcohols was achieved. The purpose of supporting the metal hydride is to increase its stability and ensure the recovery of the product at the end of the reaction. A high final fatty alcohol yield was obtained when alumina-supported NaBH<sub>4</sub> was used. The use of more than stoichiometric amounts of methanol and NaBH<sub>4</sub> is important to produce alkoxyborohydride anions that act as better reducing species than NaBH<sub>4</sub>. The reaction conditions effect was investigated and the role of short carbon chain alcohol structure was explained. The effect of fatty acid methyl ester structure was also examined. Saturated fatty acid methyl esters (methyl laurate, methyl myristate) with short carbon chains can be easily reduced using NaBH<sub>4</sub>/Al<sub>2</sub>O<sub>3</sub> and methanol, thus obtaining high conversion and selectable fuel alcohol. Unsaturated fatty acid methyl ester (methyl oleate) with longer carbon shows steric hindrance, which is not suitable for the interaction of esters and reduces the surface area, meaning that the conversion of fatty acid methyl ester is lower. <a href="/2673-4583/14/1/87">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/14/1">27th International Electronic Conference on Synthetic Organic Chemistry</a>)<br/> </div> <a href="#" class="abstract-figures-show" data-counterslink = "https://www.mdpi.com/2673-4583/14/1/87/show" ><span >►</span><span style=" display: none;">▼</span> Show Figures </a><div class="abstract-image-preview "><div class="arrow left-arrow" id="prev1317165"><i class="fa fa-caret-left"></i></div><div class="arrow right-arrow" id="next1317165"><i class="fa fa-caret-right"></i></div><div class="absgraph cycle-slideshow manual" data-cycle-fx="scrollHorz" data-cycle-timeout="0" data-cycle-next="#next1317165" data-cycle-prev="#prev1317165" data-cycle-progressive="#images1317165" data-cycle-slides=">div" data-cycle-log="false"><div class='openpopupgallery cycle-slide' data-imgindex='0' data-target='article-1317165-popup'><span class="helper"></span><img src="data:image/gif;base64,R0lGODlhAQABAAD/ACwAAAAAAQABAAACADs=" data-src="https://pub.mdpi-res.com/chemproc/chemproc-14-00087/article_deploy/html/images/chemproc-14-00087-g001-550.jpg?1705022458" alt="" style="border: 0;"><p>Figure 1</p></div><script id="images1317165" type="text/cycle" data-cycle-split="---"><div class='openpopupgallery' data-imgindex='1' data-target='article-1317165-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00087/article_deploy/html/images/chemproc-14-00087-g002-550.jpg?1705022458'><p>Figure 2</p></div> --- <div class='openpopupgallery' data-imgindex='2' data-target='article-1317165-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00087/article_deploy/html/images/chemproc-14-00087-g003-550.jpg?1705022459'><p>Figure 3</p></div> --- <div class='openpopupgallery' data-imgindex='3' data-target='article-1317165-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00087/article_deploy/html/images/chemproc-14-00087-g004-550.jpg?1705022460'><p>Figure 4</p></div> --- <div class='openpopupgallery' data-imgindex='4' data-target='article-1317165-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00087/article_deploy/html/images/chemproc-14-00087-g005-550.jpg?1705022460'><p>Figure 5</p></div> --- <div class='openpopupgallery' data-imgindex='5' data-target='article-1317165-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00087/article_deploy/html/images/chemproc-14-00087-sch001-550.jpg?1705022461'><p>Scheme 1</p></div></script></div></div><div id="article-1317165-popup" class="popupgallery" style="display: inline; line-height: 200%"><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00087/article_deploy/html/images/chemproc-14-00087-g001-550.jpg?1705022458" title=" <strong>Figure 1</strong><br/> <p>Effect of supporting NaBH<sub>4</sub>.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/87'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00087/article_deploy/html/images/chemproc-14-00087-g002-550.jpg?1705022458" title=" <strong>Figure 2</strong><br/> <p>Effect of varying ML/NaBH<sub>4</sub> molar ratio.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/87'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00087/article_deploy/html/images/chemproc-14-00087-g003-550.jpg?1705022459" title=" <strong>Figure 3</strong><br/> <p>Effect of varying methanol/NaBH<sub>4</sub> molar ratio.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/87'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00087/article_deploy/html/images/chemproc-14-00087-g004-550.jpg?1705022460" title=" <strong>Figure 4</strong><br/> <p>Effect of short carbon chain alcohol structure.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/87'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00087/article_deploy/html/images/chemproc-14-00087-g005-550.jpg?1705022460" title=" <strong>Figure 5</strong><br/> <p>Effect of FAME structure.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/87'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00087/article_deploy/html/images/chemproc-14-00087-sch001-550.jpg?1705022461" title=" <strong>Scheme 1</strong><br/> <p>Stoichiometry of FOL synthesis reaction using FAME, methanol and sodium borhydride.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/87'>Full article</a></strong> "></a></div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 2555 KiB   </span> <a href="/2673-4583/14/1/96/pdf?version=1706079741" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="Synthesis and Characterisation of Thymol-Based Hydrophobic Deep Eutectic Solvents" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/14/1/96">Synthesis and Characterisation of Thymol-Based Hydrophobic Deep Eutectic Solvents</a> <div class="authors"> by <span class="inlineblock "><strong>Deborah Oluwatomilola Adeoye</strong>, </span><span class="inlineblock "><strong>Zaharaddeen Sani Gano</strong>, </span><span class="inlineblock "><strong>Omar Umar Ahmed</strong>, </span><span class="inlineblock "><strong>Suleiman Mohammed Shuwa</strong>, </span><span class="inlineblock "><strong>Abdulazeez Yusuf Atta</strong> and </span><span class="inlineblock "><strong>Baba Yakubu Jubril</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2023</b>, <em>14</em>(1), 96; <a href="https://doi.org/10.3390/ecsoc-27-16380">https://doi.org/10.3390/ecsoc-27-16380</a> - 29 Nov 2023 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-cropped inline"> The evolution of Hydrophobic Deep Eutectic Solvents (HDESs) has expanded the applications of the new generation of solvents, known as Deep Eutectic Solvents (DES), to include water-based operations. How stable they are in aqueous media qualifies them to be categorised as hydrophobic. This <a href="#" data-counterslink = "https://www.mdpi.com/2673-4583/14/1/96/more" onclick="$(this).parents('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> [...] Read more.</a> </div> <div class="abstract-full "> The evolution of Hydrophobic Deep Eutectic Solvents (HDESs) has expanded the applications of the new generation of solvents, known as Deep Eutectic Solvents (DES), to include water-based operations. How stable they are in aqueous media qualifies them to be categorised as hydrophobic. This also determines whether they are appropriate materials for water-based industrial processes or not or whether they end up constituting a greater pollution load than those processes due to the leaching of their precursors into the aqueous media when used. This work sought to prepare HDESs from a monoterpene (thymol), and three long-chain organic acids (octanoic acid, decanoic acid, and dodecanoic acid). The physicochemical characteristics of the prepared HDESs were investigated. Thereafter, their moisture absorption capacity and stability in an aqueous environment were determined to ascertain whether they are hydrophobic as predicted. <a href="/2673-4583/14/1/96">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/14/1">27th International Electronic Conference on Synthetic Organic Chemistry</a>)<br/> </div> <a href="#" class="abstract-figures-show" data-counterslink = "https://www.mdpi.com/2673-4583/14/1/96/show" ><span >►</span><span style=" display: none;">▼</span> Show Figures </a><div class="abstract-image-preview "><div class="arrow left-arrow" id="prev1325295"><i class="fa fa-caret-left"></i></div><div class="arrow right-arrow" id="next1325295"><i class="fa fa-caret-right"></i></div><div class="absgraph cycle-slideshow manual" data-cycle-fx="scrollHorz" data-cycle-timeout="0" data-cycle-next="#next1325295" data-cycle-prev="#prev1325295" data-cycle-progressive="#images1325295" data-cycle-slides=">div" data-cycle-log="false"><div class='openpopupgallery cycle-slide' data-imgindex='0' data-target='article-1325295-popup'><span class="helper"></span><img src="data:image/gif;base64,R0lGODlhAQABAAD/ACwAAAAAAQABAAACADs=" data-src="https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g001-550.jpg?1706079836" alt="" style="border: 0;"><p>Figure 1</p></div><script id="images1325295" type="text/cycle" data-cycle-split="---"><div class='openpopupgallery' data-imgindex='1' data-target='article-1325295-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g002-550.jpg?1706079836'><p>Figure 2</p></div> --- <div class='openpopupgallery' data-imgindex='2' data-target='article-1325295-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g003-550.jpg?1706079837'><p>Figure 3</p></div> --- <div class='openpopupgallery' data-imgindex='3' data-target='article-1325295-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g004-550.jpg?1706079837'><p>Figure 4</p></div> --- <div class='openpopupgallery' data-imgindex='4' data-target='article-1325295-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g005-550.jpg?1706079837'><p>Figure 5</p></div> --- <div class='openpopupgallery' data-imgindex='5' data-target='article-1325295-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g006-550.jpg?1706079838'><p>Figure 6</p></div> --- <div class='openpopupgallery' data-imgindex='6' data-target='article-1325295-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g007-550.jpg?1706079838'><p>Figure 7</p></div> --- <div class='openpopupgallery' data-imgindex='7' data-target='article-1325295-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g008-550.jpg?1706079839'><p>Figure 8</p></div> --- <div class='openpopupgallery' data-imgindex='8' data-target='article-1325295-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g009-550.jpg?1706079839'><p>Figure 9</p></div></script></div></div><div id="article-1325295-popup" class="popupgallery" style="display: inline; line-height: 200%"><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g001-550.jpg?1706079836" title=" <strong>Figure 1</strong><br/> <p>FTIR spectra of thymol, Octanoic acid, and TC<sub>8</sub> HDESs.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/96'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g002-550.jpg?1706079836" title=" <strong>Figure 2</strong><br/> <p>FTIR spectra of thymol, Decanoic acid, and TC<sub>10</sub> HDESs.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/96'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g003-550.jpg?1706079837" title=" <strong>Figure 3</strong><br/> <p>FTIR spectra of thymol, Dodecanoic acid, and TC<sub>12</sub> HDESs.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/96'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g004-550.jpg?1706079837" title=" <strong>Figure 4</strong><br/> <p>Density–temperature graph for thymol-based HDESs.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/96'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g005-550.jpg?1706079837" title=" <strong>Figure 5</strong><br/> <p>Viscosity–temperature graph for thymol-based HDESs.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/96'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g006-550.jpg?1706079838" title=" <strong>Figure 6</strong><br/> <p>Surface tension–temperature graph for thymol-based HDESs.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/96'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g007-550.jpg?1706079838" title=" <strong>Figure 7</strong><br/> <p>HDESs in water immediately after agitation.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/96'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g008-550.jpg?1706079839" title=" <strong>Figure 8</strong><br/> <p>HDESs in water 24 h after agitation.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/96'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00096/article_deploy/html/images/chemproc-14-00096-g009-550.jpg?1706079839" title=" <strong>Figure 9</strong><br/> <p>Percentage moisture content graph for HDESs (test for hydrophobicity).</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/96'>Full article</a></strong> "></a></div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 6 pages, 2954 KiB   </span> <a href="/2673-4583/13/1/26/pdf?version=1700804277" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="Bioavailability Computations for Natural Phenolic Derivatives for Druglikeness Assessment" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/13/1/26">Bioavailability Computations for Natural Phenolic Derivatives for Druglikeness Assessment</a> <div class="authors"> by <span class="inlineblock "><strong>Amalia Stefaniu</strong>, </span><span class="inlineblock "><strong>Lucia Camelia Pirvu</strong>, </span><span class="inlineblock "><strong>Lucia Pintilie</strong> and </span><span class="inlineblock "><strong>Sorin Constantin Godeanu</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2023</b>, <em>13</em>(1), 26; <a href="https://doi.org/10.3390/chemproc2023013026">https://doi.org/10.3390/chemproc2023013026</a> - 24 Nov 2023 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-cropped inline"> The main phenolic compounds in the <i>Hippophae rhamnoides</i> fruit with potential therapeutic activities are quercetin-3-<i>O</i>-rhamnoside, quercetin-3-<i>O</i>-galactoside, myricetin, rutin, luteolin, kaempferol, vitexin, gallic acid, chlorogenic acid, caffeic acid, 7-methoxycoumarin, p-coumaric acid, and ferulic acid. Their general features recommend them for <a href="#" data-counterslink = "https://www.mdpi.com/2673-4583/13/1/26/more" onclick="$(this).parents('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> [...] Read more.</a> </div> <div class="abstract-full "> The main phenolic compounds in the <i>Hippophae rhamnoides</i> fruit with potential therapeutic activities are quercetin-3-<i>O</i>-rhamnoside, quercetin-3-<i>O</i>-galactoside, myricetin, rutin, luteolin, kaempferol, vitexin, gallic acid, chlorogenic acid, caffeic acid, 7-methoxycoumarin, p-coumaric acid, and ferulic acid. Their general features recommend them for nutritional and therapeutic purposes, exploiting their neuroprotective and radioprotective effects. This study aims to investigate the potency of polyphenol-derived structures against dual tyrosine-regulated kinase, modulating neuroblastomas and glioblastomas in humans. Structural insights from the point of view of drug-like property assessment are also provided by Density Functional Theory (DFT) predictions on the lowest energy conformers, using the B3LYP/6-311G (d,p) method. <a href="/2673-4583/13/1/26">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/13/1">Exploratory Workshop "Innovative Cross-Sectoral Technologies", Vth Edition, Secvent Project Meeting</a>)<br/> </div> <a href="#" class="abstract-figures-show" data-counterslink = "https://www.mdpi.com/2673-4583/13/1/26/show" ><span >►</span><span style=" display: none;">▼</span> Show Figures </a><div class="abstract-image-preview "><div class="arrow left-arrow" id="prev1286717"><i class="fa fa-caret-left"></i></div><div class="arrow right-arrow" id="next1286717"><i class="fa fa-caret-right"></i></div><div class="absgraph cycle-slideshow manual" data-cycle-fx="scrollHorz" data-cycle-timeout="0" data-cycle-next="#next1286717" data-cycle-prev="#prev1286717" data-cycle-progressive="#images1286717" data-cycle-slides=">div" data-cycle-log="false"><div class='openpopupgallery cycle-slide' data-imgindex='0' data-target='article-1286717-popup'><span class="helper"></span><img src="data:image/gif;base64,R0lGODlhAQABAAD/ACwAAAAAAQABAAACADs=" data-src="https://pub.mdpi-res.com/chemproc/chemproc-13-00026/article_deploy/html/images/chemproc-13-00026-g001-550.jpg?1700804340" alt="" style="border: 0;"><p>Figure 1</p></div><script id="images1286717" type="text/cycle" data-cycle-split="---"><div class='openpopupgallery' data-imgindex='1' data-target='article-1286717-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00026/article_deploy/html/images/chemproc-13-00026-g002-550.jpg?1700804341'><p>Figure 2</p></div> --- <div class='openpopupgallery' data-imgindex='2' data-target='article-1286717-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00026/article_deploy/html/images/chemproc-13-00026-g003-550.jpg?1700804343'><p>Figure 3</p></div> --- <div class='openpopupgallery' data-imgindex='3' data-target='article-1286717-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00026/article_deploy/html/images/chemproc-13-00026-g004-550.jpg?1700804344'><p>Figure 4</p></div> --- <div class='openpopupgallery' data-imgindex='4' data-target='article-1286717-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00026/article_deploy/html/images/chemproc-13-00026-g005-550.jpg?1700804346'><p>Figure 5</p></div></script></div></div><div id="article-1286717-popup" class="popupgallery" style="display: inline; line-height: 200%"><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00026/article_deploy/html/images/chemproc-13-00026-g001-550.jpg?1700804340" title=" <strong>Figure 1</strong><br/> <p>Energy diagram of frontier molecular orbitals and their energy gap for (<b>a</b>) 7-methoxycoumarin and (<b>b</b>) apigenin-8-<span class="html-italic">C</span>-glucoside.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/26'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00026/article_deploy/html/images/chemproc-13-00026-g002-550.jpg?1700804341" title=" <strong>Figure 2</strong><br/> <p>Electrostatic potential map for (<b>a</b>) 7-methoxycoumarin and (<b>b</b>) apigenin-8-<span class="html-italic">C</span>-glucoside.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/26'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00026/article_deploy/html/images/chemproc-13-00026-g003-550.jpg?1700804343" title=" <strong>Figure 3</strong><br/> <p>Predicted logP values for the studied ligands.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/26'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00026/article_deploy/html/images/chemproc-13-00026-g004-550.jpg?1700804344" title=" <strong>Figure 4</strong><br/> <p>Predicted PSA values for the studied ligands.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/26'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00026/article_deploy/html/images/chemproc-13-00026-g005-550.jpg?1700804346" title=" <strong>Figure 5</strong><br/> <p>Hydrogen bonding formed by (<b>a</b>) 7-methoxycoumarin and (<b>b</b>) apigenin-8-<span class="html-italic">C</span>-glucoside within the active binding site of the 5ZTN fragment.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/26'>Full article</a></strong> "></a></div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 1040 KiB   </span> <a href="/2673-4583/14/1/89/pdf?version=1705307419" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="Synthesis of a Bio-Based Methacrylic Polymer Using Camphor Terpene as a Renewable Resource" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/14/1/89">Synthesis of a Bio-Based Methacrylic Polymer Using Camphor Terpene as a Renewable Resource</a> <div class="authors"> by <span class="inlineblock "><strong>Naziha Chabane</strong>, </span><span class="inlineblock "><strong>Fayçal Dergal</strong>, </span><span class="inlineblock "><strong>Hervé Pata</strong> and </span><span class="inlineblock "><strong>Ilyas Chikhi</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2023</b>, <em>14</em>(1), 89; <a href="https://doi.org/10.3390/ecsoc-27-16336">https://doi.org/10.3390/ecsoc-27-16336</a> - 23 Nov 2023 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-cropped inline"> Sustainable polymers derived from biomass have the potential to reduce environmental impacts while offering significant performance and cost advantages over petrochemical-derived macromolecules. We present here a facile and efficient approach to the synthesis of a biomethacrylic monomer, isobornyl/bornyl methacrylate (IBOMA/BOMA), using the naturally <a href="#" data-counterslink = "https://www.mdpi.com/2673-4583/14/1/89/more" onclick="$(this).parents('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> [...] Read more.</a> </div> <div class="abstract-full "> Sustainable polymers derived from biomass have the potential to reduce environmental impacts while offering significant performance and cost advantages over petrochemical-derived macromolecules. We present here a facile and efficient approach to the synthesis of a biomethacrylic monomer, isobornyl/bornyl methacrylate (IBOMA/BOMA), using the naturally available camphor terpene in the essential oil of the Algerian plant Artemisia arborescens (Absinthe) as a key intermediate. The essential oil of the aerial part of the Artemisia arborescens plant naturally distributed in northwest Algeria was isolated by hydrodistillation and analyzed using gas chromatography–mass spectrometry (GC/MS) techniques. Nine components were identified, representing 90.7% of the total content. The main constituent of Artemisia arborescens essential oil is camphor (71.8%). Camphor was purified and modified to produce an 80% renewable-carbon-based methacrylic monomer. This terpene-derived methacrylic monomer was free radically polymerized to create a biosourced methacrylic polymer. Nuclear magnetic resonance (NMR) was used to characterize the structure of camphor terpene, isobornyl/bornyl methacrylate, and poly (isobornyl/bornyl methacrylate) (PIBOMA)/(PBOMA). <a href="/2673-4583/14/1/89">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/14/1">27th International Electronic Conference on Synthetic Organic Chemistry</a>)<br/> </div> <a href="#" class="abstract-figures-show" data-counterslink = "https://www.mdpi.com/2673-4583/14/1/89/show" ><span >►</span><span style=" display: none;">▼</span> Show Figures </a><div class="abstract-image-preview "><div class="arrow left-arrow" id="prev1319263"><i class="fa fa-caret-left"></i></div><div class="arrow right-arrow" id="next1319263"><i class="fa fa-caret-right"></i></div><div class="absgraph cycle-slideshow manual" data-cycle-fx="scrollHorz" data-cycle-timeout="0" data-cycle-next="#next1319263" data-cycle-prev="#prev1319263" data-cycle-progressive="#images1319263" data-cycle-slides=">div" data-cycle-log="false"><div class='openpopupgallery cycle-slide' data-imgindex='0' data-target='article-1319263-popup'><span class="helper"></span><img src="data:image/gif;base64,R0lGODlhAQABAAD/ACwAAAAAAQABAAACADs=" data-src="https://pub.mdpi-res.com/chemproc/chemproc-14-00089/article_deploy/html/images/chemproc-14-00089-g001-550.jpg?1705307493" alt="" style="border: 0;"><p>Figure 1</p></div><script id="images1319263" type="text/cycle" data-cycle-split="---"><div class='openpopupgallery' data-imgindex='1' data-target='article-1319263-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00089/article_deploy/html/images/chemproc-14-00089-g002a-550.jpg?1705307496'><p>Figure 2</p></div> --- <div class='openpopupgallery' data-imgindex='2' data-target='article-1319263-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00089/article_deploy/html/images/chemproc-14-00089-g002b-550.jpg?1705307497'><p>Figure 2 Cont.</p></div> --- <div class='openpopupgallery' data-imgindex='3' data-target='article-1319263-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-14-00089/article_deploy/html/images/chemproc-14-00089-sch001-550.jpg?1705307498'><p>Scheme 1</p></div></script></div></div><div id="article-1319263-popup" class="popupgallery" style="display: inline; line-height: 200%"><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00089/article_deploy/html/images/chemproc-14-00089-g001-550.jpg?1705307493" title=" <strong>Figure 1</strong><br/> <p>Reduction of camphor, esterification of isoborneol/borneol, and polymerization of isobornyl/bornyl methacrylate.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/89'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00089/article_deploy/html/images/chemproc-14-00089-g002a-550.jpg?1705307496" title=" <strong>Figure 2</strong><br/> <p>NMR spectra of isobornyl/bornyl methacrylate IBOMA/BOMA: (<b>A</b>) poly (isobornyl/bornyl methacrylate) PIBOMA/PBOMA. (<b>B</b>,<b>C</b>) Raman spectra of poly (isobornyl/bornyl methacrylate) PIBOMA/PBOMA [<a href="#B16-chemproc-14-00089" class="html-bibr">16</a>].</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/89'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00089/article_deploy/html/images/chemproc-14-00089-g002b-550.jpg?1705307497" title=" <strong>Figure 2 Cont.</strong><br/> <p>NMR spectra of isobornyl/bornyl methacrylate IBOMA/BOMA: (<b>A</b>) poly (isobornyl/bornyl methacrylate) PIBOMA/PBOMA. (<b>B</b>,<b>C</b>) Raman spectra of poly (isobornyl/bornyl methacrylate) PIBOMA/PBOMA [<a href="#B16-chemproc-14-00089" class="html-bibr">16</a>].</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/89'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-14-00089/article_deploy/html/images/chemproc-14-00089-sch001-550.jpg?1705307498" title=" <strong>Scheme 1</strong><br/> <p>Diagram summarizing the stages of our work.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/14/1/89'>Full article</a></strong> "></a></div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 4 pages, 233 KiB   </span> <a href="/2673-4583/13/1/27/pdf?version=1700806218" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="Proteogenomic Tools in the Assessment of Pharmacological Effects of Natural Compounds" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/13/1/27">Proteogenomic Tools in the Assessment of Pharmacological Effects of Natural Compounds</a> <div class="authors"> by <span class="inlineblock "><strong>Radu Albulescu</strong>, </span><span class="inlineblock "><strong>Adrian Albulescu</strong>, </span><span class="inlineblock "><strong>Georgeta Caraene</strong>, </span><span class="inlineblock "><strong>Corina Bubueanu</strong>, </span><span class="inlineblock "><strong>Alice Grigore</strong>, </span><span class="inlineblock "><strong>Maria Petrescu</strong> and </span><span class="inlineblock "><strong>Roxana-Mădălina Stoica</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2023</b>, <em>13</em>(1), 27; <a href="https://doi.org/10.3390/chemproc2023013027">https://doi.org/10.3390/chemproc2023013027</a> - 23 Nov 2023 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-cropped inline"> Proteogenomics is a recently developed omics application, adding enhancing the sensitivity of proteomics, and thus making possible the detection of proteome markers in very tiny amounts of samples. Even if the filed developed only in the last 10 years, the technology is very <a href="#" data-counterslink = "https://www.mdpi.com/2673-4583/13/1/27/more" onclick="$(this).parents('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> [...] Read more.</a> </div> <div class="abstract-full "> Proteogenomics is a recently developed omics application, adding enhancing the sensitivity of proteomics, and thus making possible the detection of proteome markers in very tiny amounts of samples. Even if the filed developed only in the last 10 years, the technology is very intensely applied in clinical diagnostics, and more recently, efforts are made to use it in non-clinical, in vitro and in vivo studies. The aim of this study was to investigate the applicability of single-plex and multiplex assays in the evaluation of proteome changes generated in vitro by the exposure to several standard compounds. The extracts demonstrated weak cytotoxic effects. The detection of cytokines Performing the same assays on tissue lysates permitted only the detection of low levels of cytokines. <a href="/2673-4583/13/1/27">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/13/1">Exploratory Workshop "Innovative Cross-Sectoral Technologies", Vth Edition, Secvent Project Meeting</a>)<br/> </div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 8 pages, 5825 KiB   </span> <a href="/2673-4583/13/1/25/pdf?version=1700797206" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="Diagnosis, Photogrammetry and Conservation Treatment with Nanomaterials of Sacidava Fortress" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/13/1/25">Diagnosis, Photogrammetry and Conservation Treatment with Nanomaterials of Sacidava Fortress</a> <div class="authors"> by <span class="inlineblock "><strong>Rodica-Mariana Ion</strong>, </span><span class="inlineblock "><strong>Lorena Iancu</strong>, </span><span class="inlineblock "><strong>Ramona Marina Grigorescu</strong>, </span><span class="inlineblock "><strong>Sorin Marcel Colesniuc</strong>, </span><span class="inlineblock "><strong>Verginica Schroder</strong>, </span><span class="inlineblock "><strong>Raluca Andreea Trandafir</strong>, </span><span class="inlineblock "><strong>Silviu Ionita</strong>, </span><span class="inlineblock "><strong>Anca Irina Gheboianu</strong> and </span><span class="inlineblock "><strong>Sofia Slamnoiu-Teodorescu</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2023</b>, <em>13</em>(1), 25; <a href="https://doi.org/10.3390/chemproc2023013025">https://doi.org/10.3390/chemproc2023013025</a> - 23 Nov 2023 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-full inline"> The diagnosis, thermography, aerial photogrammetry, and conservation treatment with nanomaterials (CHAp) for some samples from Sacidava Fortress, Romania, are analyzed and the results are discussed accordingly in this paper. <a href="/2673-4583/13/1/25">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/13/1">Exploratory Workshop "Innovative Cross-Sectoral Technologies", Vth Edition, Secvent Project Meeting</a>)<br/> </div> <a href="#" class="abstract-figures-show" data-counterslink = "https://www.mdpi.com/2673-4583/13/1/25/show" ><span >►</span><span style=" display: none;">▼</span> Show Figures </a><div class="abstract-image-preview "><div class="arrow left-arrow" id="prev1286665"><i class="fa fa-caret-left"></i></div><div class="arrow right-arrow" id="next1286665"><i class="fa fa-caret-right"></i></div><div class="absgraph cycle-slideshow manual" data-cycle-fx="scrollHorz" data-cycle-timeout="0" data-cycle-next="#next1286665" data-cycle-prev="#prev1286665" data-cycle-progressive="#images1286665" data-cycle-slides=">div" data-cycle-log="false"><div class='openpopupgallery cycle-slide' data-imgindex='0' data-target='article-1286665-popup'><span class="helper"></span><img src="data:image/gif;base64,R0lGODlhAQABAAD/ACwAAAAAAQABAAACADs=" data-src="https://pub.mdpi-res.com/chemproc/chemproc-13-00025/article_deploy/html/images/chemproc-13-00025-g001-550.jpg?1700797308" alt="" style="border: 0;"><p>Figure 1</p></div><script id="images1286665" type="text/cycle" data-cycle-split="---"><div class='openpopupgallery' data-imgindex='1' data-target='article-1286665-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00025/article_deploy/html/images/chemproc-13-00025-g002-550.jpg?1700797309'><p>Figure 2</p></div> --- <div class='openpopupgallery' data-imgindex='2' data-target='article-1286665-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00025/article_deploy/html/images/chemproc-13-00025-g003-550.jpg?1700797311'><p>Figure 3</p></div> --- <div class='openpopupgallery' data-imgindex='3' data-target='article-1286665-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00025/article_deploy/html/images/chemproc-13-00025-g004-550.jpg?1700797312'><p>Figure 4</p></div> --- <div class='openpopupgallery' data-imgindex='4' data-target='article-1286665-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00025/article_deploy/html/images/chemproc-13-00025-g005-550.jpg?1700797314'><p>Figure 5</p></div> --- <div class='openpopupgallery' data-imgindex='5' data-target='article-1286665-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00025/article_deploy/html/images/chemproc-13-00025-g006-550.jpg?1700797315'><p>Figure 6</p></div> --- <div class='openpopupgallery' data-imgindex='6' data-target='article-1286665-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00025/article_deploy/html/images/chemproc-13-00025-g007-550.jpg?1700797319'><p>Figure 7</p></div> --- <div class='openpopupgallery' data-imgindex='7' data-target='article-1286665-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00025/article_deploy/html/images/chemproc-13-00025-g008-550.jpg?1700797321'><p>Figure 8</p></div></script></div></div><div id="article-1286665-popup" class="popupgallery" style="display: inline; line-height: 200%"><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00025/article_deploy/html/images/chemproc-13-00025-g001-550.jpg?1700797308" title=" <strong>Figure 1</strong><br/> <p>Collection area and their location (blue and red frames indicate the places where the samples have been collected)<b>.</b></p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/25'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00025/article_deploy/html/images/chemproc-13-00025-g002-550.jpg?1700797309" title=" <strong>Figure 2</strong><br/> <p>Variations in temperatures recorded at the surface of the analyzed stones (minimum, maximum and average values).</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/25'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00025/article_deploy/html/images/chemproc-13-00025-g003-550.jpg?1700797311" title=" <strong>Figure 3</strong><br/> <p>The thermogramms of Sacidava sample.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/25'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00025/article_deploy/html/images/chemproc-13-00025-g004-550.jpg?1700797312" title=" <strong>Figure 4</strong><br/> <p>XRD distribution of the main components.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/25'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00025/article_deploy/html/images/chemproc-13-00025-g005-550.jpg?1700797314" title=" <strong>Figure 5</strong><br/> <p>FTIR spectra of the Sacidava samples.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/25'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00025/article_deploy/html/images/chemproc-13-00025-g006-550.jpg?1700797315" title=" <strong>Figure 6</strong><br/> <p>The lichens identified on Sacidava samples <span class="html-italic">Physcia tenella</span> (<b>a</b>,<b>b</b>), <span class="html-italic">Caloplaca saxicola</span> (Hoffm.) <span class="html-italic">Norden</span> (<b>c</b>), <span class="html-italic">Rhizoplaca chrysoleuca (Sm.) Zopf sin Lecanora chrysoleuca</span> (<b>d</b>), <span class="html-italic">Aspicilia calcarea</span> (L.) <span class="html-italic">Mudd (Circinaria calcarea</span> (L.) <span class="html-italic">A. Nordin Savić &amp; Tibell)</span> (<b>e</b>), <span class="html-italic">Xanthoria parietina</span> (<b>f</b>).</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/25'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00025/article_deploy/html/images/chemproc-13-00025-g007-550.jpg?1700797319" title=" <strong>Figure 7</strong><br/> <p>Sacidava samples non-treated (<b>left</b>) and treated (<b>right</b>) with (CHAp).</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/25'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00025/article_deploy/html/images/chemproc-13-00025-g008-550.jpg?1700797321" title=" <strong>Figure 8</strong><br/> <p>The aerial image of Sacidava fortress with drone.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/25'>Full article</a></strong> "></a></div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 8 pages, 4384 KiB   </span> <a href="/2673-4583/13/1/24/pdf?version=1700799935" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="Practical Aspects of Biogenic Amines Detection" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/13/1/24">Practical Aspects of Biogenic Amines Detection</a> <div class="authors"> by <span class="inlineblock "><strong>Petru Epure</strong>, </span><span class="inlineblock "><strong>Ana-Maria Gurban</strong> and </span><span class="inlineblock "><strong>Lucian-Gabriel Zamfir</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2023</b>, <em>13</em>(1), 24; <a href="https://doi.org/10.3390/chemproc2023013024">https://doi.org/10.3390/chemproc2023013024</a> - 23 Nov 2023 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-cropped inline"> This paper presents a method for monitoring food freshness and quality through the early detection of biogenic amines, which are indicators of food spoilage/degradation. The urge to monitor food quality has led to a growing interest in the detection of toxic compounds, such <a href="#" data-counterslink = "https://www.mdpi.com/2673-4583/13/1/24/more" onclick="$(this).parents('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> [...] Read more.</a> </div> <div class="abstract-full "> This paper presents a method for monitoring food freshness and quality through the early detection of biogenic amines, which are indicators of food spoilage/degradation. The urge to monitor food quality has led to a growing interest in the detection of toxic compounds, such as biogenic amines (BAs), as chemical indicators of food degradation by using different bioanalytical tools. The bioanalytical platform includes several parts and modules useful for food hazard evaluation. This paper presents how electrochemical and spectrometric detection works for biogenic amine monitoring in food and how the communication interface provides useful data. <a href="/2673-4583/13/1/24">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/13/1">Exploratory Workshop "Innovative Cross-Sectoral Technologies", Vth Edition, Secvent Project Meeting</a>)<br/> </div> <a href="#" class="abstract-figures-show" data-counterslink = "https://www.mdpi.com/2673-4583/13/1/24/show" ><span >►</span><span style=" display: none;">▼</span> Show Figures </a><div class="abstract-image-preview "><div class="arrow left-arrow" id="prev1286689"><i class="fa fa-caret-left"></i></div><div class="arrow right-arrow" id="next1286689"><i class="fa fa-caret-right"></i></div><div class="absgraph cycle-slideshow manual" data-cycle-fx="scrollHorz" data-cycle-timeout="0" data-cycle-next="#next1286689" data-cycle-prev="#prev1286689" data-cycle-progressive="#images1286689" data-cycle-slides=">div" data-cycle-log="false"><div class='openpopupgallery cycle-slide' data-imgindex='0' data-target='article-1286689-popup'><span class="helper"></span><img src="data:image/gif;base64,R0lGODlhAQABAAD/ACwAAAAAAQABAAACADs=" data-src="https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g001-550.jpg?1700799999" alt="" style="border: 0;"><p>Figure 1</p></div><script id="images1286689" type="text/cycle" data-cycle-split="---"><div class='openpopupgallery' data-imgindex='1' data-target='article-1286689-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g002-550.jpg?1700800001'><p>Figure 2</p></div> --- <div class='openpopupgallery' data-imgindex='2' data-target='article-1286689-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g003-550.jpg?1700800002'><p>Figure 3</p></div> --- <div class='openpopupgallery' data-imgindex='3' data-target='article-1286689-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g004-550.jpg?1700800003'><p>Figure 4</p></div> --- <div class='openpopupgallery' data-imgindex='4' data-target='article-1286689-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g005-550.jpg?1700800004'><p>Figure 5</p></div> --- <div class='openpopupgallery' data-imgindex='5' data-target='article-1286689-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g006-550.jpg?1700800005'><p>Figure 6</p></div> --- <div class='openpopupgallery' data-imgindex='6' data-target='article-1286689-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g007-550.jpg?1700800005'><p>Figure 7</p></div> --- <div class='openpopupgallery' data-imgindex='7' data-target='article-1286689-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g008-550.jpg?1700800006'><p>Figure 8</p></div> --- <div class='openpopupgallery' data-imgindex='8' data-target='article-1286689-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g009-550.jpg?1700800007'><p>Figure 9</p></div> --- <div class='openpopupgallery' data-imgindex='9' data-target='article-1286689-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g010-550.jpg?1700800008'><p>Figure 10</p></div> --- <div class='openpopupgallery' data-imgindex='10' data-target='article-1286689-popup'><span class="helper"></span><img src='https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g011-550.jpg?1700800010'><p>Figure 11</p></div></script></div></div><div id="article-1286689-popup" class="popupgallery" style="display: inline; line-height: 200%"><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g001-550.jpg?1700799999" title=" <strong>Figure 1</strong><br/> <p>Modules of the detection platform.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/24'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g002-550.jpg?1700800001" title=" <strong>Figure 2</strong><br/> <p>Proposed detection chain for biogenic amines- (BA) determination in food.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/24'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g003-550.jpg?1700800002" title=" <strong>Figure 3</strong><br/> <p>Customized functionalization of multi-SPE using 2D printing.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/24'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g004-550.jpg?1700800003" title=" <strong>Figure 4</strong><br/> <p>Electrochemical module prototype using PSOC 5 and ADuCM355.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/24'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g005-550.jpg?1700800004" title=" <strong>Figure 5</strong><br/> <p>Details regarding the PSOC5 configuration.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/24'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g006-550.jpg?1700800005" title=" <strong>Figure 6</strong><br/> <p>Setup for electrochemical measurements.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/24'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g007-550.jpg?1700800005" title=" <strong>Figure 7</strong><br/> <p>Innovative cell combined measurements.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/24'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g008-550.jpg?1700800006" title=" <strong>Figure 8</strong><br/> <p>Spectrometric detection on the electrode surface using optical fiber.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/24'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g009-550.jpg?1700800007" title=" <strong>Figure 9</strong><br/> <p>Combined electrochemical and optical setup initial prototype.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/24'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g010-550.jpg?1700800008" title=" <strong>Figure 10</strong><br/> <p>Example of an electrochemical setup.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/24'>Full article</a></strong> "></a><a href="https://pub.mdpi-res.com/chemproc/chemproc-13-00024/article_deploy/html/images/chemproc-13-00024-g011-550.jpg?1700800010" title=" <strong>Figure 11</strong><br/> <p>Measurements made on different types of functionalization.</p> <strong style='display: block; margin-top: 10px; font-size: 18px;'><a style='color: #fff' href='/2673-4583/13/1/24'>Full article</a></strong> "></a></div> </div> </div> </div> <div class="expanding-div collapsed"> <div class="generic-item article-item"> <div class="article-content"> <div class="label right label__btn"> <span style="font-size: 12px; color: #1a1a1a;"> 5 pages, 224 KiB   </span> <a href="/2673-4583/13/1/23/pdf?version=1700736316" class="UD_Listings_ArticlePDF" title="Article PDF" data-name="Assessment of Pullulan, a Microbial Polysaccharide, as a Matrix for Senotherapeutics Delivery" data-journal="chemproc"> <i class="material-icons custom-download"></i> </a> </div> <div class="article-icons"><span class="label openaccess" data-dropdown="drop-article-label-openaccess" aria-expanded="false">Open Access</span><span class="label articletype">Proceeding Paper</span></div> <a class="title-link" href="/2673-4583/13/1/23">Assessment of Pullulan, a Microbial Polysaccharide, as a Matrix for Senotherapeutics Delivery</a> <div class="authors"> by <span class="inlineblock "><strong>Ramona-Daniela Pavaloiu</strong>, </span><span class="inlineblock "><strong>Fawzia Sha’at</strong>, </span><span class="inlineblock "><strong>Corina Bubueanu</strong>, </span><span class="inlineblock "><strong>Maria Petrescu</strong> and </span><span class="inlineblock "><strong>Claudia Sevcenco</strong></span> </div> <div class="color-grey-dark"> <em>Chem. Proc.</em> <b>2023</b>, <em>13</em>(1), 23; <a href="https://doi.org/10.3390/chemproc2023013023">https://doi.org/10.3390/chemproc2023013023</a> - 23 Nov 2023 </div> <div class="abstract-div"> <a href="#" onclick="$(this).next('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> <strong>Abstract </strong> </a> <div class="abstract-cropped inline"> This study’s objective was to assess pullulan, in the form of pullulan acetate, as a matrix for senotherapeutics delivery. Polymeric nanoparticles loaded with various senotherapeutics (metformin, quercitin, kaempferol, curcumin, and luteolin) were prepared via nanoprecipitation or double emulsion methods using pullulan acetate as <a href="#" data-counterslink = "https://www.mdpi.com/2673-4583/13/1/23/more" onclick="$(this).parents('.abstract-cropped').toggleClass('inline').next('.abstract-full').toggleClass('inline'); return false;"> [...] Read more.</a> </div> <div class="abstract-full "> This study’s objective was to assess pullulan, in the form of pullulan acetate, as a matrix for senotherapeutics delivery. Polymeric nanoparticles loaded with various senotherapeutics (metformin, quercitin, kaempferol, curcumin, and luteolin) were prepared via nanoprecipitation or double emulsion methods using pullulan acetate as a biodegradable polymeric matrix. Quercitin, kaempferol, curcumin, and luteolin nanoparticles showed good yield (<70%), satisfactory values of entrapment efficiency (<60%), and nanometric sizes ranging between 205 and 270 nm, with narrow dispersity and good stability at 4 °C. The formulations demonstrated that pullulan showed great potential for producing nanoparticles with application in senotherapeutics delivery. <a href="/2673-4583/13/1/23">Full article</a> </div> </div> <div class="belongsTo" style="margin-bottom: 10px;"> (This article belongs to the Proceedings of <a href="/2673-4583/13/1">Exploratory Workshop "Innovative Cross-Sectoral Technologies", Vth Edition, Secvent Project Meeting</a>)<br/> </div> </div> </div> </div> </div> <div class="generic-item last-item"> <a class="bold" href="/search?q=&journal=chemproc&sort=pubdate&page_count=50">More Articles...</a> </div> </div> </div> </div> <div id="left-column" class="content__column large-3 large-pull-6 medium-3 medium-pull-6 small-12 columns"> <div id="js-large-main-top-container"> <div id="js-main-top-container" class="content__container"> <a href="/journal/chemproc"> <img src="https://pub.mdpi-res.com/img/journals/chemproc-logo.png?e993dbe391b6414c" alt="chemproc-logo" title="Chemistry Proceedings" style="max-height: 60px; 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