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micrographs</title> <meta name="description" content="Search results for: TEM micrographs"> <meta name="keywords" content="TEM micrographs"> <meta name="viewport" content="width=device-width, initial-scale=1, minimum-scale=1, maximum-scale=1, user-scalable=no"> <meta charset="utf-8"> <link href="https://cdn.waset.org/favicon.ico" type="image/x-icon" rel="shortcut icon"> <link href="https://cdn.waset.org/static/plugins/bootstrap-4.2.1/css/bootstrap.min.css" rel="stylesheet"> <link href="https://cdn.waset.org/static/plugins/fontawesome/css/all.min.css" rel="stylesheet"> <link href="https://cdn.waset.org/static/css/site.css?v=150220211555" rel="stylesheet"> </head> <body> <header> <div class="container"> <nav class="navbar navbar-expand-lg navbar-light"> <a class="navbar-brand" href="https://waset.org"> <img src="https://cdn.waset.org/static/images/wasetc.png" alt="Open Science Research Excellence" title="Open Science Research Excellence" /> </a> <button class="d-block d-lg-none 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action="https://publications.waset.org/abstracts/search"> <div id="custom-search-input"> <div class="input-group"> <i class="fas fa-search"></i> <input type="text" class="search-query" name="q" placeholder="Author, Title, Abstract, Keywords" value="TEM micrographs"> <input type="submit" class="btn_search" value="Search"> </div> </div> </form> </div> </div> <div class="row mt-3"> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Commenced</strong> in January 2007</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Frequency:</strong> Monthly</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Edition:</strong> International</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Paper Count:</strong> 75</div> </div> </div> </div> <h1 class="mt-3 mb-3 text-center" style="font-size:1.6rem;">Search results for: TEM micrographs</h1> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">75</span> Image Processing of Scanning Electron Microscope Micrograph of Ferrite and Pearlite Steel for Recognition of Micro-Constituents</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Subir%20Gupta">Subir Gupta</a>, <a href="https://publications.waset.org/abstracts/search?q=Subhas%20Ganguly"> Subhas Ganguly</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this paper, we demonstrate the new area of application of image processing in metallurgical images to develop the more opportunity for structure-property correlation based approaches of alloy design. The present exercise focuses on the development of image processing tools suitable for phrase segmentation, grain boundary detection and recognition of micro-constituents in SEM micrographs of ferrite and pearlite steels. A comprehensive data of micrographs have been experimentally developed encompassing the variation of ferrite and pearlite volume fractions and taking images at different magnification (500X, 1000X, 15000X, 2000X, 3000X and 5000X) under scanning electron microscope. The variation in the volume fraction has been achieved using four different plain carbon steel containing 0.1, 0.22, 0.35 and 0.48 wt% C heat treated under annealing and normalizing treatments. The obtained data pool of micrographs arbitrarily divided into two parts to developing training and testing sets of micrographs. The statistical recognition features for ferrite and pearlite constituents have been developed by learning from training set of micrographs. The obtained features for microstructure pattern recognition are applied to test set of micrographs. The analysis of the result shows that the developed strategy can successfully detect the micro constitutes across the wide range of magnification and variation of volume fractions of the constituents in the structure with an accuracy of about +/- 5%. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=SEM%20micrograph" title="SEM micrograph">SEM micrograph</a>, <a href="https://publications.waset.org/abstracts/search?q=metallurgical%20image%20processing" title=" metallurgical image processing"> metallurgical image processing</a>, <a href="https://publications.waset.org/abstracts/search?q=ferrite%20pearlite%20steel" title=" ferrite pearlite steel"> ferrite pearlite steel</a>, <a href="https://publications.waset.org/abstracts/search?q=microstructure" title=" microstructure"> microstructure</a> </p> <a href="https://publications.waset.org/abstracts/71497/image-processing-of-scanning-electron-microscope-micrograph-of-ferrite-and-pearlite-steel-for-recognition-of-micro-constituents" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/71497.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">199</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">74</span> Electrochemical Behaviour of 2014 and 2024 Al-Cu-Mg Alloys of Various Tempers</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=K.%20S.%20Ghosh">K. S. Ghosh</a>, <a href="https://publications.waset.org/abstracts/search?q=Sagnik%20Bose"> Sagnik Bose</a>, <a href="https://publications.waset.org/abstracts/search?q=Kapil%20Tripati"> Kapil Tripati </a> </p> <p class="card-text"><strong>Abstract:</strong></p> Potentiodynamic polarization studies carried out on AA2024 and AA2014 Al-Cu-Mg alloys of various tempers in 3.5 wt. % NaCl and in 3.5 wt. % NaCl + 1.0 % H2O2 solution characteristic E-i curves. Corrosion potential (Ecorr) value has shifted towards more negative potential with the increase of artificial aging time. The Ecorr value for the alloy tempers has also shifted anodically in presence of H2O2 in 3.5 % NaCl solution. Further, passivity phenomenon has been observed in all the alloy tempers when tested in 3.5 wt. % NaCl solution at pH 12. Stress corrosion cracking (SCC) behaviour of friction stir weld (FSW) joint of AA2014 alloy has been studied bu slow strain rate test (SSRT) in 3.5 wt. % NaCl solution. Optical micrographs of the corroded surfaces of polarised samples showed general corrosion, extensive pitting and intergranular corrosion as well. Further, potentiodynamic cyclic polarization curves displayed wide hysteresis loop indicating that the alloy tempers are susceptible to pit growth damage. Attempts have been made to explain the variation of observed electrochemical and SCC behaviour of the alloy tempers and the electrolyte conditions with the help of microstructural features. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=AA%202014%20and%20AA%202024%20Al-C-Mg%20alloy" title="AA 2014 and AA 2024 Al-C-Mg alloy">AA 2014 and AA 2024 Al-C-Mg alloy</a>, <a href="https://publications.waset.org/abstracts/search?q=artificial%20ageing" title=" artificial ageing"> artificial ageing</a>, <a href="https://publications.waset.org/abstracts/search?q=potentiodynamic%20polarization" title=" potentiodynamic polarization"> potentiodynamic polarization</a>, <a href="https://publications.waset.org/abstracts/search?q=TEM%20micrographs" title=" TEM micrographs"> TEM micrographs</a>, <a href="https://publications.waset.org/abstracts/search?q=stress%20corrosion%20cracking%20%28SCC%29" title=" stress corrosion cracking (SCC)"> stress corrosion cracking (SCC)</a> </p> <a href="https://publications.waset.org/abstracts/17400/electrochemical-behaviour-of-2014-and-2024-al-cu-mg-alloys-of-various-tempers" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/17400.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">334</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">73</span> Synthesis and Study the Effect of HNTs on PVA/Chitosan Composite Material</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Malek%20Ali">Malek Ali</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Composites materials of Poly (vinyl alcohol) (PVA)/Chitosan (CS) have been synthesized and characterized successfully. HNTs have been added to composites to enhance the mechanical and degradation properties by hydrogen bonding interactions, compatibility, and chemical crosslink between HNTs and PVA. PVA/CS/HNTs composites prepared with different concentration ratio. SEM micrographs of composites surface showed that more agglomeration with more chitosan ratio. Mechanical and degradation properties were characterized and the result indicates that Mechanical and degradation of 80%PVA/5%Chitosan/15%HNTs higher than the others PVA/CS/HNTs composites. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=PVA%2Fchitosan" title="PVA/chitosan">PVA/chitosan</a>, <a href="https://publications.waset.org/abstracts/search?q=composites" title=" composites"> composites</a>, <a href="https://publications.waset.org/abstracts/search?q=PVA%2FCS%2FHNTs" title=" PVA/CS/HNTs"> PVA/CS/HNTs</a>, <a href="https://publications.waset.org/abstracts/search?q=HNTs" title=" HNTs"> HNTs</a> </p> <a href="https://publications.waset.org/abstracts/42719/synthesis-and-study-the-effect-of-hnts-on-pvachitosan-composite-material" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/42719.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">292</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">72</span> Zinc Oxide Nanowires: Device Fabrication and Optical Properties</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Igori%20Wallace">Igori Wallace</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Zinc oxide (ZnO) nanowires with hexagonal structure were successfully synthesized by the chemical bath deposition technique. The obtained nanowires were characterized by scanning electron microscope (SEM) and energy dispersive X-ray analysis (EDX). The SEM micrographs revealed the morphology of ZnO nanowires with the diameter between 170.3 and 481nm and showed that the normal pH of the bath solution, 8.1 is the optimized value to form ZnO nanowires with the hexagonal shape. The compositional (EDX) analysis revealed the elemental compositions of samples and confirmed the presence of Zn and O. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=crystallite" title="crystallite">crystallite</a>, <a href="https://publications.waset.org/abstracts/search?q=chemical%20bath%20deposition%20technique" title=" chemical bath deposition technique"> chemical bath deposition technique</a>, <a href="https://publications.waset.org/abstracts/search?q=hexagonal" title=" hexagonal"> hexagonal</a>, <a href="https://publications.waset.org/abstracts/search?q=morphology" title=" morphology"> morphology</a>, <a href="https://publications.waset.org/abstracts/search?q=nanowire" title=" nanowire"> nanowire</a> </p> <a href="https://publications.waset.org/abstracts/37553/zinc-oxide-nanowires-device-fabrication-and-optical-properties" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/37553.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">309</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">71</span> Fabrication of Carbon Nanoparticles and Graphene Using Pulsed Laser Ablation</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Davoud%20Dorranian">Davoud Dorranian</a>, <a href="https://publications.waset.org/abstracts/search?q=Hajar%20Sadeghi"> Hajar Sadeghi</a>, <a href="https://publications.waset.org/abstracts/search?q=Elmira%20Solati"> Elmira Solati </a> </p> <p class="card-text"><strong>Abstract:</strong></p> Carbon nanostructures in various forms were synthesized using pulsed laser ablation of a graphite target in different liquid environment. The beam of a Q-switched Nd:YAG laser of 1064-nm wavelength at 7-ns pulse width is employed to irradiate the solid target in water, acetone, alcohol, and cetyltrimethylammonium bromide (CTAB). Then the effect of the liquid environment on the characteristic of carbon nanostructures produced by laser ablation was investigated. The optical properties of the carbon nanostructures were examined at room temperature by UV–Vis-NIR spectrophotometer. The crystalline structure of the carbon nanostructures was analyzed by X-ray diffraction (XRD). The morphology of samples was investigated by field emission scanning electron microscope (FE-SEM). Transmission electron microscope (TEM) was employed to investigate the form of carbon nanostructures. Raman spectroscopy was used to determine the quality of carbon nanostructures. Results show that different carbon nanostructures such as nanoparticles and few-layer graphene were formed in various liquid environments. The UV-Vis-NIR absorption spectra of samples reveal that the intensity of absorption peak of nanoparticles in alcohol is higher than the other liquid environments due to the larger number of nanoparticles in this environment. The red shift of the absorption peak of the sample in acetone confirms that produced carbon nanoparticles in this liquid are averagely larger than the other medium. The difference in the intensity and shape of the absorption peak indicated the effect of the liquid environment in producing the nanoparticles. The XRD pattern of the sample in water indicates an amorphous structure due to existence the graphene sheets. X-ray diffraction pattern shows that the degree of crystallinity of sample produced in CTAB is higher than the other liquid environments. Transmission electron microscopy images reveal that the generated carbon materials in water are graphene sheet and in the other liquid environments are graphene sheet and spherical nanostructures. According to the TEM images, we have the larger amount of carbon nanoparticles in the alcohol environment. FE-SEM micrographs indicate that in this liquids sheet like structures are formed however in acetone, produced sheets are adhered and these layers overlap with each other. According to the FE-SEM micrographs, the surface morphology of the sample in CTAB was coarser than that without surfactant. From Raman spectra, it can be concluded the distinct shape, width, and position of the graphene peaks and corresponding graphite source. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=carbon%20nanostructures" title="carbon nanostructures">carbon nanostructures</a>, <a href="https://publications.waset.org/abstracts/search?q=graphene" title=" graphene"> graphene</a>, <a href="https://publications.waset.org/abstracts/search?q=pulsed%20laser%20ablation" title=" pulsed laser ablation"> pulsed laser ablation</a>, <a href="https://publications.waset.org/abstracts/search?q=graphite" title=" graphite"> graphite</a> </p> <a href="https://publications.waset.org/abstracts/36792/fabrication-of-carbon-nanoparticles-and-graphene-using-pulsed-laser-ablation" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/36792.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">315</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">70</span> Wet Spun Graphene Fibers With Silver Nanoparticles For Flexible Electronic Applications </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Syed%20W.%20Hasan">Syed W. Hasan</a>, <a href="https://publications.waset.org/abstracts/search?q=Zhiqun%20Tian"> Zhiqun Tian</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Wet spinning provides a facile and economic route to fabricate graphene nanofibers (GFs) on mass scale. Nevertheless, the pristine GFs exhibit significantly low electrical and mechanical properties owing to stacked graphene sheets and weak inter-atomic bonding. In this report, we present highly conductive Ag-decorated-GFs (Ag/GFs). The SEM micrographs show Ag nanoparticles (NPs) (dia ~10 nm) are homogeneously distributed throughout the cross-section of the fiber. The Ag NPs provide a conductive network for the electrons flow raising the conductivity to 1.8(10^4) S/m which is 4 times higher than the pristine GFs. Our results surpass the conductivities of graphene fibers doped with CNTs, Nanocarbon, fullerene, and Cu. The chemical and structural attributes of Ag/GFs are further elucidated through XPS, AFM and Raman spectroscopy. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ag%20nanoparticles" title="Ag nanoparticles">Ag nanoparticles</a>, <a href="https://publications.waset.org/abstracts/search?q=Conductive%20fibers" title=" Conductive fibers"> Conductive fibers</a>, <a href="https://publications.waset.org/abstracts/search?q=Graphene" title=" Graphene"> Graphene</a>, <a href="https://publications.waset.org/abstracts/search?q=Wet%20spinning" title=" Wet spinning"> Wet spinning</a> </p> <a href="https://publications.waset.org/abstracts/122583/wet-spun-graphene-fibers-with-silver-nanoparticles-for-flexible-electronic-applications" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/122583.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">142</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">69</span> Morphological Process of Villi Detachment Assessed by Computer-Assisted 3D Reconstruction of Intestinal Crypt from Serial Ultrathin Sections of Rat Duodenum Mucosa</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Lise%20P.%20Lab%C3%A9jof">Lise P. Labéjof</a>, <a href="https://publications.waset.org/abstracts/search?q=Ivna%20Moror%C3%B3"> Ivna Mororó</a>, <a href="https://publications.waset.org/abstracts/search?q=Raquel%20G.%20Bastos"> Raquel G. Bastos</a>, <a href="https://publications.waset.org/abstracts/search?q=Maria%20Isabel%20G.%20Severo"> Maria Isabel G. Severo</a>, <a href="https://publications.waset.org/abstracts/search?q=Arno%20H.%20de%20Oliveira"> Arno H. de Oliveira</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This work presents an alternative mode of intestine mucosa renewal that may allow to better understand the total loss of villi after irradiation. It was tested a morphological method of 3d reconstruction using micrographs of serial sections of rat duodenum. We used hundreds of sections of each specimen of duodenum placed on glass slides and examined under a light microscope. Those containing the detachment, approximately a dozen, were chosen for observation under a transmission electron microscope (TEM). Each of these sections was glued on a block of epon resin and recut into a hundred of 60 nm-thick sections. Ribbons of these ultrathin sections were distributed on a series of copper grids in the same order of appearance than during the process of microstomia. They were then stained by solutions of uranyl and lead salts and observed under a TEM. The sections were pictured and the electron micrographs showing signs of cells detachment were transferred into two softwares, ImageJ to align the cellular structures and Reconstruct to realize the 3d reconstruction. It has been detected epithelial cells that exhibited all signs of programmed cell death and localized at the villus-crypt junction. Their nucleus was irregular in shape with a condensed chromatin in clumps. Their cytoplasm was darker than that of neighboring cells, containing many swollen mitochondria. In some places of the sections, we could see intercellular spaces enlarged by the presence of shrunk cells which displayed a plasma membrane with an irregular shape in thermowell as if the cell interdigitations would distant from each other. The three-dimensional reconstruction of the crypts has allowed observe gradual loss of intercellular contacts of crypt cells in the longitudinal plan of the duodenal mucosa. In the transverse direction, there was a gradual increase of the intercellular space as if these cells moved away from one another. This observation allows assume that the gradual remoteness of the cells at the villus-crypt junction is the beginning of the mucosa detachment. Thus, the shrinking of cells due to apoptosis is the way that they detach from the mucosa and progressively the villi also. These results are in agreement with our initial hypothesis and thus have demonstrated that the villi become detached from the mucosa at the villus-crypt junction by the programmed cell death process. This type of loss of entire villus helps explain the rapid denudation of the intestinal mucosa in case of irradiation. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=3dr" title="3dr">3dr</a>, <a href="https://publications.waset.org/abstracts/search?q=transmission%20electron%20microscopy" title=" transmission electron microscopy"> transmission electron microscopy</a>, <a href="https://publications.waset.org/abstracts/search?q=ionizing%20radiations" title=" ionizing radiations"> ionizing radiations</a>, <a href="https://publications.waset.org/abstracts/search?q=rat%20small%20intestine" title=" rat small intestine"> rat small intestine</a>, <a href="https://publications.waset.org/abstracts/search?q=apoptosis" title=" apoptosis"> apoptosis</a> </p> <a href="https://publications.waset.org/abstracts/41139/morphological-process-of-villi-detachment-assessed-by-computer-assisted-3d-reconstruction-of-intestinal-crypt-from-serial-ultrathin-sections-of-rat-duodenum-mucosa" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/41139.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">378</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">68</span> Investigation of Zinc Corrosion in Tropical Soil Solution</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=M.%20Lebrini">M. Lebrini</a>, <a href="https://publications.waset.org/abstracts/search?q=L.%20Salhi"> L. Salhi</a>, <a href="https://publications.waset.org/abstracts/search?q=C.%20Deyrat"> C. Deyrat</a>, <a href="https://publications.waset.org/abstracts/search?q=C.%20Roos"> C. Roos</a>, <a href="https://publications.waset.org/abstracts/search?q=O.%20Nait-Rabah"> O. Nait-Rabah</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The paper presents a large experimental study on the corrosion of zinc in tropical soil and in the ground water at the various depths. Through this study, the corrosion rate prediction was done on the basis of two methods the electrochemical method and the gravimetric. The electrochemical results showed that the corrosion rate is more important at the depth levels 0 m to 0.5 m and 0.5 m to 1 m and beyond these depth levels, the corrosion rate is less important. The electrochemical results indicated also that a passive layer is formed on the zinc surface. The found SEM and EDX micrographs displayed that the surface is extremely attacked and confirmed that a zinc oxide layer is present on the surface whose thickness and relief increase as the contact with soil increases. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=soil%20corrosion" title="soil corrosion">soil corrosion</a>, <a href="https://publications.waset.org/abstracts/search?q=galvanized%20steel" title=" galvanized steel"> galvanized steel</a>, <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20technique" title=" electrochemical technique"> electrochemical technique</a>, <a href="https://publications.waset.org/abstracts/search?q=SEM%20and%20EDX" title=" SEM and EDX"> SEM and EDX</a> </p> <a href="https://publications.waset.org/abstracts/153148/investigation-of-zinc-corrosion-in-tropical-soil-solution" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/153148.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">128</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">67</span> Optimization of Hydrogel Conductive Nanocomposite as Solar Cell</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Shimaa%20M.%20Elsaeed">Shimaa M. Elsaeed</a>, <a href="https://publications.waset.org/abstracts/search?q=Reem%20K.%20Farag"> Reem K. Farag</a>, <a href="https://publications.waset.org/abstracts/search?q=Ibrahim%20M.%20Nassar"> Ibrahim M. Nassar</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Hydrogel conductive polymer nanocomposite fabricated via in-situ polymerization of polyaniline (PANI) inside thermosensitive hydrogels based on hydroxy ethyl meth acrylate (HEMA) copolymer with 2-acrylamido-2-methyl propane sulfonic acid (AMPS). SEM micrographs show the nanometric size of the conductive material (polyaniline, PANI) dispersed in the hydrogel matrix. The swelling parameters of hydrogel are measured. The incorporation of PANI improves the mechanical properties and swelling up to 30,000% without breaking. X-ray diffraction shows that typical polyaniline crystallization is formed in composite, which is advantageous to increase the electrical conductivity of the composite hydrogel. Open-circuit voltage (I-V) curve fill factor of the highest photo-conversion efficiency and enhanced to use in solar cell. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=hydrogel" title="hydrogel">hydrogel</a>, <a href="https://publications.waset.org/abstracts/search?q=solar%20cell" title=" solar cell"> solar cell</a>, <a href="https://publications.waset.org/abstracts/search?q=conductive%20polymer" title=" conductive polymer"> conductive polymer</a>, <a href="https://publications.waset.org/abstracts/search?q=nanocomposite" title=" nanocomposite"> nanocomposite</a> </p> <a href="https://publications.waset.org/abstracts/42489/optimization-of-hydrogel-conductive-nanocomposite-as-solar-cell" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/42489.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">399</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">66</span> Assessing the Antimicrobial Activity of Chitosan Nanoparticles by Fluorescence-Labeling</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Laidson%20P.%20Gomes">Laidson P. Gomes</a>, <a href="https://publications.waset.org/abstracts/search?q=Cristina%20T.%20Andrade"> Cristina T. Andrade</a>, <a href="https://publications.waset.org/abstracts/search?q=Eduardo%20M.%20Del%20Aguila"> Eduardo M. Del Aguila</a>, <a href="https://publications.waset.org/abstracts/search?q=Cameron%20Alexander"> Cameron Alexander</a>, <a href="https://publications.waset.org/abstracts/search?q=V%C3%A2nia%20M.%20F.%20Paschoalin"> Vânia M. F. Paschoalin</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Chitosan is a natural polysaccharide prepared by the N-deacetylation of chitin. In this study, the physicochemical and antibacterial properties of chitosan nanoparticles, produced by ultrasound irradiation, were evaluated. The physicochemical properties of the nanoparticles were determined by dynamic light scattering and zeta potential analysis. Chitosan nanoparticles inhibited the growth of <em>E. coli</em>. The minimum inhibitory concentration (MIC) values were lower than 0.5 mg/mL, and the minimum bactericidal concentration (MBC) values were similar or higher than MIC values. Confocal laser scanning micrographs (CLSM) were used to observe the interaction between <em>E. coli </em>suspensions mixed with FITC-labeled chitosan polymers and nanoparticles. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=chitosan%20nanoparticles" title="chitosan nanoparticles">chitosan nanoparticles</a>, <a href="https://publications.waset.org/abstracts/search?q=dynamic%20light%20scattering" title=" dynamic light scattering"> dynamic light scattering</a>, <a href="https://publications.waset.org/abstracts/search?q=zeta%20potential" title=" zeta potential"> zeta potential</a>, <a href="https://publications.waset.org/abstracts/search?q=confocal%20microscopy" title=" confocal microscopy"> confocal microscopy</a>, <a href="https://publications.waset.org/abstracts/search?q=antibacterial%20activity" title=" antibacterial activity"> antibacterial activity</a> </p> <a href="https://publications.waset.org/abstracts/84752/assessing-the-antimicrobial-activity-of-chitosan-nanoparticles-by-fluorescence-labeling" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/84752.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">501</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">65</span> Mechanical Properties and Microstructure of Ultra-High Performance Concrete Containing Fly Ash and Silica Fume</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Jisong%20Zhang">Jisong Zhang</a>, <a href="https://publications.waset.org/abstracts/search?q=Yinghua%20Zhao"> Yinghua Zhao</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The present study investigated the mechanical properties and microstructure of Ultra-High Performance Concrete (UHPC) containing supplementary cementitious materials (SCMs), such as fly ash (FA) and silica fume (SF), and to verify the synergistic effect in the ternary system. On the basis of 30% fly ash replacement, the incorporation of either 10% SF or 20% SF show a better performance compared to the reference sample. The efficiency factor (k-value) was calculated as a synergistic effect to predict the compressive strength of UHPC with these SCMs. The SEM of micrographs and pore volume from BJH method indicate a high correlation with compressive strength. Further, an artificial neural networks model was constructed for prediction of the compressive strength of UHPC containing these SCMs. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=artificial%20neural%20network" title="artificial neural network">artificial neural network</a>, <a href="https://publications.waset.org/abstracts/search?q=fly%20ash" title=" fly ash"> fly ash</a>, <a href="https://publications.waset.org/abstracts/search?q=mechanical%20properties" title=" mechanical properties"> mechanical properties</a>, <a href="https://publications.waset.org/abstracts/search?q=ultra-high%20performance%20concrete" title=" ultra-high performance concrete"> ultra-high performance concrete</a> </p> <a href="https://publications.waset.org/abstracts/57551/mechanical-properties-and-microstructure-of-ultra-high-performance-concrete-containing-fly-ash-and-silica-fume" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/57551.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">414</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">64</span> Functionalization and Dispersion of Multiwall Carbon Nanotubes in Waterborne Polyurethane</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Shahla%20Hajializadeh">Shahla Hajializadeh</a>, <a href="https://publications.waset.org/abstracts/search?q=Maryam%20Hamedanlou"> Maryam Hamedanlou</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Multiwall carbon nanotubes were chemically modified with amide groups for the purpose of enhancing their chemical affinity with waterborne polyurethane. In this study, a thermoplastic nanocomposite containing functionalized multiwall carbon nanotube/waterborne polyurethane (WBPU/MWNT) via in situ polymerization has been prepared. The impacts of MWNT addition on the morphology and electrical properties of nanocomposites were investigated. Micrographs of Scanning Electron Microscopy (SEM) prove that functionalized CNT can be effectively dispersed in WBPU matrix. The electrical conductivity of nanocomposites increased with the CNT contents in as such the nanocomposites containing 1 wt% of MWNT exhibited a conductivity nearly five orders of magnitude higher than the WBPU film. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=chemical%20functionalization" title="chemical functionalization">chemical functionalization</a>, <a href="https://publications.waset.org/abstracts/search?q=electrical%20properties" title=" electrical properties"> electrical properties</a>, <a href="https://publications.waset.org/abstracts/search?q=in%20situ%20polymerization" title=" in situ polymerization"> in situ polymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=morphology" title=" morphology"> morphology</a>, <a href="https://publications.waset.org/abstracts/search?q=multiwall%20carbon%20nanotubes" title=" multiwall carbon nanotubes"> multiwall carbon nanotubes</a>, <a href="https://publications.waset.org/abstracts/search?q=waterborne%20polyurethane" title=" waterborne polyurethane"> waterborne polyurethane</a> </p> <a href="https://publications.waset.org/abstracts/55470/functionalization-and-dispersion-of-multiwall-carbon-nanotubes-in-waterborne-polyurethane" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/55470.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">266</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">63</span> Photocatalytic Oxidation of Gaseous Formaldehyde Using the TiO2 Coated SF Filter</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Janjira%20Triped">Janjira Triped</a>, <a href="https://publications.waset.org/abstracts/search?q=Wipada%20Sanongraj"> Wipada Sanongraj</a>, <a href="https://publications.waset.org/abstracts/search?q=Wipawee%20Khamwichit"> Wipawee Khamwichit</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The research work covered in this study includes the morphological structure and optical properties of TiO2-coated silk fibroin (SF) filters at 2.5% wt. TiO2/vol. PVA solution. SEM micrographs revealed the fibrous morphology of the TiO2-coated SF filters. An average diameter of the SF fiber was estimated to be approximately 10µm. Also, it was confirmed that TiO2 can be adhered more on SF filter surface at higher TiO2 dosages. The activity of semiconductor materials was studied by UV-VIS spectrophotometer method. The spectral data recorded shows the strong cut off at 390 nm. The calculated band-gap energy was about 3.19 eV. The photocatalytic activity of the filter was tested for gaseous formaldehyde removal in a modeling room with the total volume of 2.66 m3. The highest removal efficiency (54.72 ± 1.75%) was obtained at the initial formaldehyde concentration of about 5.00 ± 0.50ppm. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=photocatalytic%20oxidation%20process" title="photocatalytic oxidation process">photocatalytic oxidation process</a>, <a href="https://publications.waset.org/abstracts/search?q=formaldehyde%20%28HCHO%29" title=" formaldehyde (HCHO)"> formaldehyde (HCHO)</a>, <a href="https://publications.waset.org/abstracts/search?q=silk%20fibroin%20%28SF%29" title=" silk fibroin (SF)"> silk fibroin (SF)</a>, <a href="https://publications.waset.org/abstracts/search?q=titanium%20dioxide%20%28TiO2%29" title=" titanium dioxide (TiO2)"> titanium dioxide (TiO2)</a> </p> <a href="https://publications.waset.org/abstracts/4845/photocatalytic-oxidation-of-gaseous-formaldehyde-using-the-tio2-coated-sf-filter" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/4845.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">469</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">62</span> Optical and Magnetic Properties of Ferromagnetic Co-Ni Co-Doped TiO2 Thin Films</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Rabah%20Bensaha">Rabah Bensaha</a>, <a href="https://publications.waset.org/abstracts/search?q=Badreddine%20Toubal"> Badreddine Toubal</a> </p> <p class="card-text"><strong>Abstract:</strong></p> We investigate the structural, optical and magnetic properties of TiO2, Co-doped TiO2, Ni-doped TiO2 and Co-Ni co-doped TiO2 thin films prepared by the sol-gel dip coating method. Fully anatase phase was obtained by adding metal ions without any detectable impurity phase or oxide formed. AFM and SEM micrographs clearly confirm that the addition of Co-Ni affects the shape of anatase nanoparticles. The crystallite sizes and surface roughness of TiO2 films increase with Co-doping, Ni-doping and Co–Ni co-doping, respectively. The refractive index, thickness and optical band gap values of the films were obtained by means of optical transmittance spectra measurements. The band gap of TiO2 sample was decreased by Co-doping, Ni-doping and Co–Ni co-doping TiO2 films. Both undoped and Co-Ni co-doped films were found to be ferromagnetic at room temperature may due to the presence of oxygen vacancy defect and the probable formation of metal clusters Co-Ni. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Co-Ni%20co-doped" title="Co-Ni co-doped">Co-Ni co-doped</a>, <a href="https://publications.waset.org/abstracts/search?q=anatase%20TiO2" title=" anatase TiO2"> anatase TiO2</a>, <a href="https://publications.waset.org/abstracts/search?q=ferromagnetic" title=" ferromagnetic"> ferromagnetic</a>, <a href="https://publications.waset.org/abstracts/search?q=sol-gel%20method" title=" sol-gel method"> sol-gel method</a>, <a href="https://publications.waset.org/abstracts/search?q=thin%20films" title=" thin films"> thin films</a> </p> <a href="https://publications.waset.org/abstracts/35968/optical-and-magnetic-properties-of-ferromagnetic-co-ni-co-doped-tio2-thin-films" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/35968.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">444</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">61</span> Characterization and Evaluation of the Dissolution Increase of Molecular Solid Dispersions of Efavirenz</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Leslie%20Raphael%20de%20M.%20Ferraz">Leslie Raphael de M. Ferraz</a>, <a href="https://publications.waset.org/abstracts/search?q=Salvana%20Priscylla%20M.%20Costa"> Salvana Priscylla M. Costa</a>, <a href="https://publications.waset.org/abstracts/search?q=Tarcyla%20de%20A.%20Gomes"> Tarcyla de A. Gomes</a>, <a href="https://publications.waset.org/abstracts/search?q=Giovanna%20Christinne%20R.%20M.%20Schver"> Giovanna Christinne R. M. Schver</a>, <a href="https://publications.waset.org/abstracts/search?q=Crist%C3%B3v%C3%A3o%20R.%20da%20Silva"> Cristóvão R. da Silva</a>, <a href="https://publications.waset.org/abstracts/search?q=Magaly%20Andreza%20M.%20de%20Lyra"> Magaly Andreza M. de Lyra</a>, <a href="https://publications.waset.org/abstracts/search?q=Danilo%20Augusto%20F.%20Fontes"> Danilo Augusto F. Fontes</a>, <a href="https://publications.waset.org/abstracts/search?q=Larissa%20A.%20Rolim"> Larissa A. Rolim</a>, <a href="https://publications.waset.org/abstracts/search?q=Amanda%20Carla%20Q.%20M.%20Vieira"> Amanda Carla Q. M. Vieira</a>, <a href="https://publications.waset.org/abstracts/search?q=Miracy%20M.%20de%20Albuquerque"> Miracy M. de Albuquerque</a>, <a href="https://publications.waset.org/abstracts/search?q=Pedro%20J.%20Rolim-Neto"> Pedro J. Rolim-Neto</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Efavirenz (EFV) is a drug used as first-line treatment of AIDS. However, it has poor aqueous solubility and wettability, presenting problems in the gastrointestinal tract absorption and bioavailability. One of the most promising strategies to improve the solubility is the use of solid dispersions (SD). Therefore, this study aimed to characterize SD EFZ with the polymers: PVP-K30, PVPVA 64 and SOLUPLUS in order to find an optimal formulation to compose a future pharmaceutical product for AIDS therapy. Initially, Physical Mixtures (PM) and SD with the polymers were obtained containing 10, 20, 50 and 80% of drug (w/w) by the solvent method. The best formulation obtained between the SD was selected by in vitro dissolution test. Finally, the drug-carrier system chosen, in all ratios obtained, were analyzed by the following techniques: Differential Scanning Calorimetry (DSC), polarization microscopy, Scanning Electron Microscopy (SEM) and spectrophotometry of absorption in the region of infrared (IR). From the dissolution profiles of EFV, PM and SD, the values of area Under The Curve (AUC) were calculated. The data showed that the AUC of all PM is greater than the isolated EFV, this result is derived from the hydrophilic properties of the polymers thus favoring a decrease in surface tension between the drug and the dissolution medium. In adittion, this ensures an increasing of wettability of the drug. In parallel, it was found that SD whom had higher AUC values, were those who have the greatest amount of polymer (with only 10% drug). As the amount of drug increases, it was noticed that these results either decrease or are statistically similar. The AUC values of the SD using the three different polymers, followed this decreasing order: SD PVPVA 64-EFV 10% > SD PVP-K30-EFV 10% > SD Soluplus®-EFV 10%. The DSC curves of SD’s did not show the characteristic endothermic event of drug melt process, suggesting that the EFV was converted to its amorphous state. The analysis of polarized light microscopy showed significant birefringence of the PM’s, but this was not observed in films of SD’s, thus suggesting the conversion of the drug from the crystalline to the amorphous state. In electron micrographs of all PM, independently of the percentage of the drug, the crystal structure of EFV was clearly detectable. Moreover, electron micrographs of the SD with the two polymers in different ratios investigated, we observed the presence of particles with irregular size and morphology, also occurring an extensive change in the appearance of the polymer, not being possible to differentiate the two components. IR spectra of PM corresponds to the overlapping of polymer and EFV bands indicating thereby that there is no interaction between them, unlike the spectra of all SD that showed complete disappearance of the band related to the axial deformation of the NH group of EFV. Therefore, this study was able to obtain a suitable formulation to overcome the solubility limitations of the EFV, since SD PVPVA 64-EFZ 10% was chosen as the best system in delay crystallization of the prototype, reaching higher levels of super saturation. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=characterization" title="characterization">characterization</a>, <a href="https://publications.waset.org/abstracts/search?q=dissolution" title=" dissolution"> dissolution</a>, <a href="https://publications.waset.org/abstracts/search?q=Efavirenz" title=" Efavirenz"> Efavirenz</a>, <a href="https://publications.waset.org/abstracts/search?q=solid%20dispersions" title=" solid dispersions"> solid dispersions</a> </p> <a href="https://publications.waset.org/abstracts/25685/characterization-and-evaluation-of-the-dissolution-increase-of-molecular-solid-dispersions-of-efavirenz" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/25685.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">631</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">60</span> Effects of Applied Pressure and Heat Treatment on the Microstructure of Squeeze Cast Al-Si Alloy Were Examined</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mohamed%20Ben%20Amar">Mohamed Ben Amar</a>, <a href="https://publications.waset.org/abstracts/search?q=Henda%20Barhoumi"> Henda Barhoumi</a>, <a href="https://publications.waset.org/abstracts/search?q=Hokia%20Siala"> Hokia Siala</a>, <a href="https://publications.waset.org/abstracts/search?q=Foued%20Elhalouani"> Foued Elhalouani</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The present contribution consists of a purely experimental investigation on the effect of Squeeze casting on the micro structural and mechanical propriety of Al-Si alloys destined to automotive industry. Accordingly, we have proceeding, by ourselves, to all the thermal treatment consisting of solution treatment at 540°C for 8h and aging at 160°C for 4h. The various thermal treatment, have been carried out in order to monitor the processes of formation and dissolution accompanying the solid state phase transformations as well as the resulting changes in the mechanical proprieties. The examination of the micrographs of the aluminum alloys reveals the dominant presence of dendrite. Concerning the mechanical characteristic the Vickers micro-hardness curve an increase as a function of the pressure. As well as the heat treatment increase mechanical propriety such that pressure and micro hardness. The curves have been explained in terms of structural hardening resulting from the various compounds formation. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=squeeze%20casting" title="squeeze casting">squeeze casting</a>, <a href="https://publications.waset.org/abstracts/search?q=process%20parameters" title=" process parameters"> process parameters</a>, <a href="https://publications.waset.org/abstracts/search?q=heat%20treatment" title=" heat treatment"> heat treatment</a>, <a href="https://publications.waset.org/abstracts/search?q=ductility" title=" ductility"> ductility</a>, <a href="https://publications.waset.org/abstracts/search?q=microstructure" title=" microstructure"> microstructure</a> </p> <a href="https://publications.waset.org/abstracts/35915/effects-of-applied-pressure-and-heat-treatment-on-the-microstructure-of-squeeze-cast-al-si-alloy-were-examined" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/35915.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">431</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">59</span> Construction and Application of Zr-MCM41 Nanoreactors as Highly Active and Efficiently Catalyst in the Synthesis of Biginelli-Type Compounds</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Zohreh%20Derikvand">Zohreh Derikvand</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Nanoreactors Zr-MCM-41were prepared via the reaction of ZrOCl2, Fumed silica, sodium hydroxide and cethyltrimethyl ammonium bromide under hydrothermal condition. The prepared nanoreactors were characterized by FT-IR spectroscopy, X-ray diffraction (XRD), Scanning electron micrographs (SEM) and nitrogen adsorption-desorption. The XRD pattern of Zr-MCM-41 exhibits a high-intensity (100) and two low-intensity reflections (110 and 200) which are characteristic of hexagonal structure, exhibiting the long-range order and good textural uniformity of mesoporous structure. Based on the green chemistry approach, we report an efficient and environmentally benign protocol to study the catalytic activity of Zr-MCM-41 in the Biginelli type reactions initially. Nanoreactors Zr-MCM-41 were used as highly recoverable and reusable catalyst for synthesis of 3,4-dihydropyrimidin-2(1H)-one, octahydroquinazolinone, benzimidazolo-quinazolineone and 4,6-diarylpyrimidin-2(1H)-one. The methodology offers several advantages such as short reaction time, high yields and simple operation. The catalyst was active up to three cycles. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Zr-MCM-41%20nanoreactors" title="Zr-MCM-41 nanoreactors">Zr-MCM-41 nanoreactors</a>, <a href="https://publications.waset.org/abstracts/search?q=Biginelli%20like%20reactions" title=" Biginelli like reactions"> Biginelli like reactions</a>, <a href="https://publications.waset.org/abstracts/search?q=3" title=" 3"> 3</a>, <a href="https://publications.waset.org/abstracts/search?q=4-dihydropyrimidin-2%281H%29-ones" title="4-dihydropyrimidin-2(1H)-ones">4-dihydropyrimidin-2(1H)-ones</a>, <a href="https://publications.waset.org/abstracts/search?q=ctahydroquinazolinones" title=" ctahydroquinazolinones"> ctahydroquinazolinones</a> </p> <a href="https://publications.waset.org/abstracts/55267/construction-and-application-of-zr-mcm41-nanoreactors-as-highly-active-and-efficiently-catalyst-in-the-synthesis-of-biginelli-type-compounds" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/55267.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">206</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">58</span> Investigation of Self-Assembling of Maghemite Nanoparticles into Chain–Like Structures Using Birefringence Measurements</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=C.%20R.%20Stein%3B%20K.%20Skeff%20Neto">C. R. Stein; K. Skeff Neto</a>, <a href="https://publications.waset.org/abstracts/search?q=K.%20L.%20C.%20Miranda"> K. L. C. Miranda</a>, <a href="https://publications.waset.org/abstracts/search?q=P.%20P.%20C.%20Sartoratto"> P. P. C. Sartoratto</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20E.%20Xavier"> M. E. Xavier</a>, <a href="https://publications.waset.org/abstracts/search?q=Z.%20G.%20M.%20Lacava"> Z. G. M. Lacava</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20M.%20De%20Freita"> S. M. De Freita</a>, <a href="https://publications.waset.org/abstracts/search?q=P.%20C.%20Morais"> P. C. Morais</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this study, static magnetic birefringence (SMB) and transmission electron microscopy (TEM) were used to investigate the self-assembling of maghemite nanoparticles suspended as biocompatible magnetic fluid (BMF) while incubated or not with the Black Eyed–Pea Trypsin Chymotripsin Inhibitor–BTCI protein. The stock samples herein studied are dextran coated maghemite nanoparticles (average core diameter of 7.1 nm, diameter dispersion of 0.26, and containing 4.6×1016 particle/mL) and the dextran coated maghemite nanoparticles associated with the BTCI protein. Several samples were prepared by diluting the stock samples with deionized water while following their colloidal stability. The diluted samples were investigated using SMB measurements to assess the average sizes of the self-assembled and suspended mesoscopic structures whereas the TEM micrographs provide the morphology of the as-suspended units. The SMB data were analyzed using a model that includes the particle-particle interaction within the mean field model picture. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biocompatible%20magnetic%20fluid" title="biocompatible magnetic fluid">biocompatible magnetic fluid</a>, <a href="https://publications.waset.org/abstracts/search?q=maghemite%20nanoparticles" title=" maghemite nanoparticles"> maghemite nanoparticles</a>, <a href="https://publications.waset.org/abstracts/search?q=self-assembling" title=" self-assembling"> self-assembling</a> </p> <a href="https://publications.waset.org/abstracts/29090/investigation-of-self-assembling-of-maghemite-nanoparticles-into-chain-like-structures-using-birefringence-measurements" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/29090.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">480</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">57</span> The Role of Nano Glass Flakes on Morphology, Dynamic-Mechanical Properties and Crystallization Behavior of Poly (Ethylene Terephthalate)</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Fatemeh%20Alsadat%20Miri">Fatemeh Alsadat Miri</a>, <a href="https://publications.waset.org/abstracts/search?q=Morteza%20Ehsani"> Morteza Ehsani</a>, <a href="https://publications.waset.org/abstracts/search?q=Hossein%20Ali%20Khonakdar"> Hossein Ali Khonakdar</a>, <a href="https://publications.waset.org/abstracts/search?q=Behjat%20Kavyani"> Behjat Kavyani</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This paper studies the effect of nano glass flakes on morphology, dynamic-mechanical properties, and crystallization behavior of poly (ethylene terephthalate) (PET). The concentration of nano glass flakes was varied from 0.5, 1, 2, and 3% wt of the total formulation. Scanning electron microscopy (SEM) micrographs showed the poor distribution of nano-glass flake particles in PET, as well as low adhesion of particles to the polymer matrix. According to differential scanning calorimetry (DSC), the crystallization rate and crystallization temperature of PET were increased by the addition of nano glass flakes. The crystallization rate of PET was increased from 31.41% to 34.25% by the incorporation of 1%wt of nano glass flakes. Based on the results of the dynamic-mechanical analysis, the storage modulus of PET gets increased by adding nano glass flakes, especially below glass transition temperature (Tg). The glass transition of PET did not change remarkably with the addition of nano glass flakes. Moreover, the use of nano glass flakes reduced the impact strength of PET. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=PET" title="PET">PET</a>, <a href="https://publications.waset.org/abstracts/search?q=nano%20glass%20flakes" title=" nano glass flakes"> nano glass flakes</a>, <a href="https://publications.waset.org/abstracts/search?q=morphology" title=" morphology"> morphology</a>, <a href="https://publications.waset.org/abstracts/search?q=crystallization" title=" crystallization"> crystallization</a> </p> <a href="https://publications.waset.org/abstracts/126266/the-role-of-nano-glass-flakes-on-morphology-dynamic-mechanical-properties-and-crystallization-behavior-of-poly-ethylene-terephthalate" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/126266.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">127</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">56</span> Preparation and in vitro Characterisation of Chitosan/Hydroxyapatite Injectable Microspheres as Hard Tissue Substitution</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=H.%20Maachou">H. Maachou</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20Chagnes"> A. Chagnes</a>, <a href="https://publications.waset.org/abstracts/search?q=G.%20Cote"> G. Cote </a> </p> <p class="card-text"><strong>Abstract:</strong></p> The present work reports the properties of chitosan/hydroxyapatite (Cs/HA: 100/00, 70/30 and 30/70) composite microspheres obtained by emulsification processing route. The morphology of chitosane microspheres was observed by a scanning electron microscope (SEM) which shows an aggregate of spherical microspheres with a particle size, determined by optical microscope, ranged from 4 to 10 µm. Thereafter, a biomimetic approach was used to study the in vitro biomineralization of these composites. It concerns the composites immersion in simulated body fluid (SBF) for different times. The deposited calcium phosphate was studied using X-ray diffraction analysis (XRD), FTIR spectroscopy and ICP analysis of phosphorus. In fact, the mineral formed on Cs/HA microspheres was a mixture of carbonated HA and β-TCP as showed by FTIR peaks at 1419,5 and 871,8 cm-1 and XRD peak at 29,5°. This formation was induced by the presence of HA in chitosan microspheres. These results are confirmed by SEM micrographs which chow the Ca-P crystals growth in form of cauliflowers. So, these materials are of great interest for bone regeneration applications due to their ability to nucleate calcium phosphates in presence of simulated body fluid (SBF). <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=hydroxyapatite" title="hydroxyapatite">hydroxyapatite</a>, <a href="https://publications.waset.org/abstracts/search?q=chitosan" title=" chitosan"> chitosan</a>, <a href="https://publications.waset.org/abstracts/search?q=microsphere" title=" microsphere"> microsphere</a>, <a href="https://publications.waset.org/abstracts/search?q=composite" title=" composite"> composite</a>, <a href="https://publications.waset.org/abstracts/search?q=bone%20regeneration" title=" bone regeneration"> bone regeneration</a> </p> <a href="https://publications.waset.org/abstracts/12735/preparation-and-in-vitro-characterisation-of-chitosanhydroxyapatite-injectable-microspheres-as-hard-tissue-substitution" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/12735.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">330</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">55</span> Development of Hydrophobic Coatings on Aluminum Alloy 7075</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Nauman%20A.%20Siddiqui">Nauman A. Siddiqui</a> </p> <p class="card-text"><strong>Abstract:</strong></p> High performance requirement of aircrafts and marines industry demands to cater major industrial problems like wetting, high-speed efficiency, and corrosion resistance. These problems can be resolved by producing the hydrophobic surfaces on the metal substrate. By anodization process, the surface of AA 7075 has been modified and achieved a rough surface with a porous aluminum oxide (Al2O3) structure at nano-level. This surface modification process reduces the surface contact energy and increases the liquid contact angle which ultimately enhances the anti-icing properties. Later the Silane and Polyurethane (PU) coatings on the anodized surface have produced a contact angle of 130°. The results showed a good water repellency and self-cleaning properties. Using SEM analysis, micrographs revealed the round nano-porous oxide structure on the substrate. Therefore this technique can help in increasing the speed efficiency by reducing the friction with the outer interaction and can also be declared as a green technique since it is user-friendly. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=AA%207075" title="AA 7075">AA 7075</a>, <a href="https://publications.waset.org/abstracts/search?q=hydrophobicity" title=" hydrophobicity"> hydrophobicity</a>, <a href="https://publications.waset.org/abstracts/search?q=silanes" title=" silanes"> silanes</a>, <a href="https://publications.waset.org/abstracts/search?q=polyurethane" title=" polyurethane"> polyurethane</a>, <a href="https://publications.waset.org/abstracts/search?q=anodization" title=" anodization"> anodization</a> </p> <a href="https://publications.waset.org/abstracts/68034/development-of-hydrophobic-coatings-on-aluminum-alloy-7075" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/68034.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">277</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">54</span> Fabrication of a Continuous Flow System for Biofilm Studies</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mohammed%20Jibrin%20Ndejiko">Mohammed Jibrin Ndejiko</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Modern and current models such as flow cell technology which enhances a non-destructive growth and inspection of the sessile microbial communities revealed a great understanding of biofilms. A continuous flow system was designed to evaluate possibility of biofilm formation by Escherichia coli DH5α on the stainless steel (type 304) under continuous nutrient supply. The result of the colony forming unit (CFU) count shows that bacterial attachment and subsequent biofilm formation on stainless steel coupons with average surface roughness of 1.5 ± 1.8 µm and 2.0 ± 0.09 µm were both significantly higher (p ≤ 0.05) than those of the stainless steel coupon with lower surface roughness of 0.38 ± 1.5 µm. These observations support the hypothesis that surface profile is one of the factors that influence biofilm formation on stainless steel surfaces. The SEM and FESEM micrographs of the stainless steel coupons also revealed the attached Escherichia coli DH5α biofilm and dehydrated extracellular polymeric substance on the stainless steel surfaces. Thus, the fabricated flow system represented a very useful tool to study biofilm formation under continuous nutrient supply. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biofilm" title="biofilm">biofilm</a>, <a href="https://publications.waset.org/abstracts/search?q=flowcell" title=" flowcell"> flowcell</a>, <a href="https://publications.waset.org/abstracts/search?q=stainless%20steel" title=" stainless steel"> stainless steel</a>, <a href="https://publications.waset.org/abstracts/search?q=coupon" title=" coupon"> coupon</a> </p> <a href="https://publications.waset.org/abstracts/49119/fabrication-of-a-continuous-flow-system-for-biofilm-studies" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/49119.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">318</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">53</span> Modified Surface Morphology, Structure and Enhanced Weathering Performance of Polyester-Urethane/Organoclay Nanocomposite Coatings</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Gaurav%20Verma">Gaurav Verma </a> </p> <p class="card-text"><strong>Abstract:</strong></p> Organoclay loaded (0-5 weight %) polyester-urethane (PU) coatings were prepared with a branched hydroxyl-bearing polyester and an aliphatic poly-isocyanate. TEM micrographs show partial exfoliation and intercalation of clay platelets in organoclay-polyester dispersions. AFM surface images reveals that the PU hard domains tend to regularise and also self-organise into spherical shapes of sizes 50 nm (0 wt %), 60 nm (2 wt %) and 190 nm (4 wt %) respectively. IR analysis shows that PU chains have increasing tendency to interact with exfoliated clay platelets through hydrogen bonding. This interaction strengthens inter-chain linkages in PU matrix and hence improves anti-ageing properties. 1000 hours of accelerated weathering was evaluated by ATR spectroscopy, while yellowing and overall discoloration was quantified by the Δb* and ΔE* values of the CIELab colour scale. Post-weathering surface properties also showed improvement as the loss of thickness and reduction in gloss in neat PU was 25% and 42%; while it was just 3.5% and 14% respectively for the 2 wt% nanocomposite coating. This work highlights the importance of modifying surface and bulk properties of PU coatings at nanoscale, which led to improved performance in accelerated weathering conditions. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=coatings" title="coatings">coatings</a>, <a href="https://publications.waset.org/abstracts/search?q=AFM" title=" AFM"> AFM</a>, <a href="https://publications.waset.org/abstracts/search?q=ageing" title=" ageing"> ageing</a>, <a href="https://publications.waset.org/abstracts/search?q=spectroscopy" title=" spectroscopy"> spectroscopy</a> </p> <a href="https://publications.waset.org/abstracts/9552/modified-surface-morphology-structure-and-enhanced-weathering-performance-of-polyester-urethaneorganoclay-nanocomposite-coatings" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/9552.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">454</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">52</span> The Effect of Si Content on the Physical Properties of Nanostructured (Ni75Fe25)100-xSix Alloy Elaborated by Mechanical Alloying</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=A.%20Kaibi">A. Kaibi</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20Guittoum"> A. Guittoum</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Hemmous"> M. Hemmous</a>, <a href="https://publications.waset.org/abstracts/search?q=D.%20Mart%C3%ADnez-Blanco"> D. Martínez-Blanco</a>, <a href="https://publications.waset.org/abstracts/search?q=P.%20Gorria"> P. Gorria</a>, <a href="https://publications.waset.org/abstracts/search?q=J.%20A.%20Blanco"> J. A. Blanco</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Kechouane"> M. Kechouane</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The present work deals with the effect of Si content on the physical properties of nanostructured (Ni75Fe25)100-x Six (x=0, 3.5, 6.5, 9, 12, and 15 at %) powders elaborated by mechanical alloying for a milling time of 96 h. The microstructure, hyperfine, and magnetic properties of the powders were investigated as a function of Si content by means of X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), Mössbauer Spectroscopy, and Vibrating Sample magnetometry (VSM). From XRD spectra, the formation of FCC disordered Ni (Fe,Si) solid solution was evidenced after 96 h. As Si content increases, the lattice parameter and the grain size decrease (from ~28 to 15 nm), while the microstrain level decreases from 0.98% to 0.65%. From SEM micrographs, we showed that powder particles become round in shape and decrease in size with increasing Si content. For all Si content, the adjustment of Mössbauer spectra confirmed the formation of a disordered ferromagnetic NiFeSi phase. From hysteresis curves, we have extracted the values of saturation magnetization and coercive field for all powders. The evolution of Ms and Hc as a function of Si content will be discussed. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=nanostructured%20powders" title="nanostructured powders">nanostructured powders</a>, <a href="https://publications.waset.org/abstracts/search?q=%28Ni75Fe25%29100-xSix%20alloy" title=" (Ni75Fe25)100-xSix alloy"> (Ni75Fe25)100-xSix alloy</a>, <a href="https://publications.waset.org/abstracts/search?q=microstructure" title=" microstructure"> microstructure</a>, <a href="https://publications.waset.org/abstracts/search?q=magnetic%20properties" title=" magnetic properties"> magnetic properties</a> </p> <a href="https://publications.waset.org/abstracts/192107/the-effect-of-si-content-on-the-physical-properties-of-nanostructured-ni75fe25100-xsix-alloy-elaborated-by-mechanical-alloying" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/192107.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">27</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">51</span> Enhancing Anode Performance in Li-S Batteries via Coating with Waste Battery-Derived Materials</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mohsen%20Hajian%20Foroushani">Mohsen Hajian Foroushani</a>, <a href="https://publications.waset.org/abstracts/search?q=Samane%20Maroufi"> Samane Maroufi</a>, <a href="https://publications.waset.org/abstracts/search?q=Rasoul%20Khayyam%20Nekouei"> Rasoul Khayyam Nekouei</a>, <a href="https://publications.waset.org/abstracts/search?q=Veena%20Sahajwalla"> Veena Sahajwalla</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Lithium (Li) metal possesses outstanding characteristics, with the highest specific capacity (3860 mAh g-1) and the lowest electrochemical potential (-3.04 V vs. SHE) among available metal anodes. The collaborative impact of Li and sulfur, featuring a specific capacity of 1670 mAh g-1, positions Li–S batteries (LSBs) as highly promising contenders for the next generation of high-energy-density batteries. However, the comprehensive commercialization of LSBs relies on addressing various challenges inherent to these batteries. One of the most formidable hurdles is the widespread issue of Li dendrite nucleation and growth on the anode surface, stemming from the inherent instability of the solid electrolyte interphase (SEI) layer. In this study, we employed a Zn-based coating derived from waste materials, significantly enhancing the performance of the symmetrical cell across various current densities. The applied coating not only improved the cyclability of the cell by more than fourfold but also reduced the charge transfer resistance from over 300 to less than 10 before cycling. Examination through SEM micrographs of both samples revealed the successful suppression of Li dendrites by the applied coating. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Li-S%20batteries" title="Li-S batteries">Li-S batteries</a>, <a href="https://publications.waset.org/abstracts/search?q=Li%20dendrite" title=" Li dendrite"> Li dendrite</a>, <a href="https://publications.waset.org/abstracts/search?q=sustainability" title=" sustainability"> sustainability</a>, <a href="https://publications.waset.org/abstracts/search?q=Li%20anode" title=" Li anode"> Li anode</a> </p> <a href="https://publications.waset.org/abstracts/178806/enhancing-anode-performance-in-li-s-batteries-via-coating-with-waste-battery-derived-materials" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/178806.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">73</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">50</span> Solvent Free Microwave Extraction of Essential Oils: A Clean Chemical Processing in the Teaching and Research Laboratory</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=M.%20A.%20Ferhat">M. A. Ferhat</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20N.%20Boukhatem"> M. N. Boukhatem</a>, <a href="https://publications.waset.org/abstracts/search?q=F.%20Chemat"> F. Chemat</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Microwave Clevenger or microwave accelerated distillation (MAD) is a combination of microwave heating and distillation, performed at atmospheric pressure without added any solvent or water. Isolation and concentration of volatile compounds are performed by a single stage. MAD extraction of orange essential oil was studied using fresh orange peel from Valencia late cultivar oranges as the raw material. MAD has been compared with a conventional technique, which used a Clevenger apparatus with hydro-distillation (HD). MAD and HD were compared in term of extraction time, yields, chemical composition and quality of the essential oil, efficiency and costs of the process. Extraction of essential oils from orange peels with MAD was better in terms of energy saving, extraction time (30 min versus 3 h), oxygenated fraction (11.7% versus 7.9%), product yield (0.42% versus 0.39%) and product quality. Orange peels treated by MAD and HD were observed by scanning electronic microscopy (SEM). Micrographs provide evidence of more rapid opening of essential oil glands treated by MAD, in contrast to conventional hydro-distillation. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=clevenger" title="clevenger">clevenger</a>, <a href="https://publications.waset.org/abstracts/search?q=microwave" title=" microwave"> microwave</a>, <a href="https://publications.waset.org/abstracts/search?q=extraction%3B%20hydro-distillation" title=" extraction; hydro-distillation"> extraction; hydro-distillation</a>, <a href="https://publications.waset.org/abstracts/search?q=essential%20oil" title=" essential oil"> essential oil</a>, <a href="https://publications.waset.org/abstracts/search?q=orange%20peel" title=" orange peel"> orange peel</a> </p> <a href="https://publications.waset.org/abstracts/37240/solvent-free-microwave-extraction-of-essential-oils-a-clean-chemical-processing-in-the-teaching-and-research-laboratory" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/37240.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">350</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">49</span> Tribological Performance of Polymer Syntactic Foams in Low-Speed Conditions</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=R.%20Narasimha%20Rao">R. Narasimha Rao</a>, <a href="https://publications.waset.org/abstracts/search?q=Ch.%20Sri%20Chaitanya"> Ch. Sri Chaitanya</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Syntactic foams are closed-cell foams with high specific strength and high compression strength. At Low speeds, the wear rate is sensitive to the sliding speeds and other tribological parameters like applied load and the sliding distance. In the present study, the tribological performance of the polymer-based syntactic foams was reported based on the experiments conducted on a pin-on-disc tribometer. The syntactic foams were manufactured with epoxy as the matrix and the cenospheres obtained from the thermal powerplants as the reinforcement. The experiments were conducted at a sliding speed of the 1 m/s. The applied load was varied from 1 kg to 5 kg up to a sliding distance of 3000 m. The wear rate increased with the sliding distance at lower loads. The trend was reversed at higher loads of 5kg. This may be due to the high plastic deformation at the initial stages when higher loads were applied. This was evident with the higher friction constants for the higher loads. The adhesive wear was found to be predominant for lower loads, while the abrasive wear tracks can be seen in micrographs of samples tested under higher loads. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=sliding%20speed" title="sliding speed">sliding speed</a>, <a href="https://publications.waset.org/abstracts/search?q=syntactic%20foams" title=" syntactic foams"> syntactic foams</a>, <a href="https://publications.waset.org/abstracts/search?q=tribological%20performance" title=" tribological performance"> tribological performance</a>, <a href="https://publications.waset.org/abstracts/search?q=wear%20rate" title=" wear rate"> wear rate</a> </p> <a href="https://publications.waset.org/abstracts/169677/tribological-performance-of-polymer-syntactic-foams-in-low-speed-conditions" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/169677.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">78</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">48</span> Blend of Polyamide 6 with Polybutylene Terephthalate Compatibilized with Epoxidized Natural Rubber (ENR-25) and N Butyl Acrylate Glycidyl Methacrylate Ethylene (EBa-GMA)</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ramita%20Vongrat">Ramita Vongrat</a>, <a href="https://publications.waset.org/abstracts/search?q=Pornsri%20Sapsrithong"> Pornsri Sapsrithong</a>, <a href="https://publications.waset.org/abstracts/search?q=Manit%20Nithitanakul"> Manit Nithitanakul</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this work, blends of polyamide 6 (PA6) and polybutylene terephthalate (PBT) were successfully prepared. The effect of epoxidized natural rubber (ENR-25) and n butyl acrylate glycidyl methacrylate ethylene (EBa-GMA) as a compatibilizer on properties of PA6/PBT blends was also investigated by varying amount of ENR-50 and EBa-GMA, i.e., 0, 0.1, 0.5, 5 and 10 phr. All blends were prepared and shaped by using twin-screw extruder at 230 °C and injection molding machine, respectively. All test specimens were characterized by phase morphology, impact strength, tensile, flexural properties, and hardness. The results exhibited that phase morphology of PA6/PBT blend without compatibilizer was incompatible. This could be attributed to poor interfacial adhesion between the two polymers. SEM micrographs showed that the addition of ENR-25 and EBa-GMA improved the compatibility of PA6/PBT blends. With the addition of ENR-50 as a compatibilizer, the uniformity and the maximum reduction of dispersed phase size were observed. Additionally, the results indicate that, as the amount of ENR-25 increased, and EBa-GMA increased, the mechanical properties, including stress at the peak, tensile modulus, and izod impact strength, were also improved. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=EBa-GMA" title="EBa-GMA">EBa-GMA</a>, <a href="https://publications.waset.org/abstracts/search?q=epoxidized%20natural%20rubber-25" title=" epoxidized natural rubber-25"> epoxidized natural rubber-25</a>, <a href="https://publications.waset.org/abstracts/search?q=polyamide%206" title=" polyamide 6"> polyamide 6</a>, <a href="https://publications.waset.org/abstracts/search?q=polybutylene%20terephthalate" title=" polybutylene terephthalate"> polybutylene terephthalate</a> </p> <a href="https://publications.waset.org/abstracts/124860/blend-of-polyamide-6-with-polybutylene-terephthalate-compatibilized-with-epoxidized-natural-rubber-enr-25-and-n-butyl-acrylate-glycidyl-methacrylate-ethylene-eba-gma" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/124860.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">169</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">47</span> A Novel Bio-ceramic Using Hyperthermia for Bone Cancer Therapy, Ferro-substituted Silicate Calcium Materials</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=hassan%20gheisari">hassan gheisari</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Ferro silicate calcium nano particles are prepared through the sol-gel method using polyvinyl alcohol (PVA) as a chelating agent. The powder, as prepared, is annealed at three different temperatures (900 ºC, 1000 ºC, and 1100 ºC) for 3 h. The XRD patterns of the samples indicate broad peaks, and the full width at half maximum decreased with increasing annealing temperature. FTIR spectra of the samples confirm the presence of metal - oxygen complexes within the structure. The average particle size obtained from PSA curve demonstrates ultrafine particles. SEM micrographs indicate the particles synthesized have spherical morphology. The saturation magnetization (Ms) and remnant magnetization (Mr) of the samples show dependence on particle size and crystallinity of the samples. The highest saturation magnetization is achieved for the sample annealed at 1100 ºC having maximum average particle size. The high saturation magnetization of the samples suggests the present method is suitable for obtaining nano particles magnetic ferro bioceramic, which is desirable for practical applications such as hyperthermia bone cancer therapy. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=hyperthermia" title="hyperthermia">hyperthermia</a>, <a href="https://publications.waset.org/abstracts/search?q=bone%20cancer" title=" bone cancer"> bone cancer</a>, <a href="https://publications.waset.org/abstracts/search?q=bio%20ceramic%3B%20magnetic%20materials%3B%20sol%E2%80%93%20gel" title=" bio ceramic; magnetic materials; sol– gel"> bio ceramic; magnetic materials; sol– gel</a>, <a href="https://publications.waset.org/abstracts/search?q=silicate%20calcium" title=" silicate calcium"> silicate calcium</a> </p> <a href="https://publications.waset.org/abstracts/163836/a-novel-bio-ceramic-using-hyperthermia-for-bone-cancer-therapy-ferro-substituted-silicate-calcium-materials" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/163836.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">73</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">46</span> Ferro-Substituted Silicate Calcium Materials, a Novel Bio-Ceramic Using Hyperthermia for Bone Cancer Therapy</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hassan%20Gheisari">Hassan Gheisari</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Ferro silicate calcium nano particles are prepared through the sol-gel method using polyvinyl alcohol (PVA) as a chelating agent. The powder as prepared is annealed at three different temperatures (900 ºC, 1000 ºC and 1100 ºC) for 3 h. The XRD patterns of the samples indicate broad peaks and the full width at half maximum decreased with increasing annealing temperature. FTIR spectra of the samples confirm the presence of metal - oxygen complexes within the structure. The average particle size obtained from PSA curve demonstrates ultrafine particles. SEM micrographs indicate the particles synthesized have spherical morphology. The saturation magnetization (Ms) and remnant magnetization (Mr) of the samples show dependence on particle size and crystallinity of the samples. The highest saturation magnetization is achieved for the sample annealed at 1100 ºC having maximum average particle size. The high saturation magnetization of the samples suggests the present method is suitable for obtaining nano particles magnetic ferro bioceramic which is desirable for practical applications such as hyperthermia bone cancer therapy. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=hyperthermia" title="hyperthermia">hyperthermia</a>, <a href="https://publications.waset.org/abstracts/search?q=bone%20cancer" title=" bone cancer"> bone cancer</a>, <a href="https://publications.waset.org/abstracts/search?q=bio%20ceramic" title=" bio ceramic"> bio ceramic</a>, <a href="https://publications.waset.org/abstracts/search?q=magnetic%20materials" title=" magnetic materials"> magnetic materials</a>, <a href="https://publications.waset.org/abstracts/search?q=sol%E2%80%93%20gel" title=" sol– gel"> sol– gel</a>, <a href="https://publications.waset.org/abstracts/search?q=silicate%20calcium" title=" silicate calcium"> silicate calcium</a> </p> <a href="https://publications.waset.org/abstracts/39463/ferro-substituted-silicate-calcium-materials-a-novel-bio-ceramic-using-hyperthermia-for-bone-cancer-therapy" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/39463.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">308</span> </span> </div> </div> <ul class="pagination"> <li class="page-item disabled"><span class="page-link">&lsaquo;</span></li> <li class="page-item active"><span class="page-link">1</span></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=TEM%20micrographs&page=2">2</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=TEM%20micrographs&page=3">3</a></li> <li class="page-item"><a class="page-link" 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