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Search results for: solvent thermal method
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21886</div> </div> </div> </div> <h1 class="mt-3 mb-3 text-center" style="font-size:1.6rem;">Search results for: solvent thermal method</h1> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">21886</span> Different Methods of Fe3O4 Nano Particles Synthesis</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Arezoo%20Hakimi">Arezoo Hakimi</a>, <a href="https://publications.waset.org/abstracts/search?q=Afshin%20Farahbakhsh"> Afshin Farahbakhsh</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Herein, we comparison synthesized Fe3O4 using, hydrothermal method, Mechanochemical processes and solvent thermal method. The Hydrothermal Technique has been the most popular one, gathering interest from scientists and technologists of different disciplines, particularly in the last fifteen years. In the hydrothermal method Fe3O4 microspheres, in which many nearly monodisperse spherical particles with diameters of about 400nm, in the mechanochemical method regular morphology indicates that the particles are well crystallized and in the solvent thermal method Fe3O4 nanoparticles have good properties of uniform size and good dispersion. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Fe3O4%20nanoparticles" title="Fe3O4 nanoparticles">Fe3O4 nanoparticles</a>, <a href="https://publications.waset.org/abstracts/search?q=hydrothermal%20method" title=" hydrothermal method"> hydrothermal method</a>, <a href="https://publications.waset.org/abstracts/search?q=mechanochemical%20processes" title=" mechanochemical processes"> mechanochemical processes</a>, <a href="https://publications.waset.org/abstracts/search?q=solvent%20thermal%20method" title=" solvent thermal method"> solvent thermal method</a> </p> <a href="https://publications.waset.org/abstracts/46580/different-methods-of-fe3o4-nano-particles-synthesis" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/46580.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">351</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">21885</span> Using the Transient Plane Source Method for Measuring Thermal Parameters of Electroceramics</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Peter%20Krupa">Peter Krupa</a>, <a href="https://publications.waset.org/abstracts/search?q=Svetoz%C3%A1r%20Malinari%C4%8D"> Svetozár Malinarič</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Transient plane source method has been used to measure the thermal diffusivity and thermal conductivity of a compact isostatic electro-ceramics at room temperature. The samples were fired at temperatures from 100 up to 1320 degrees Celsius in steps of 50. Bulk density and specific heat capacity were also measured with their corresponding standard uncertainties. The results were compared with further thermal analysis (dilatometry and thermogravimetry). Structural processes during firing were discussed. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=TPS%20method" title="TPS method">TPS method</a>, <a href="https://publications.waset.org/abstracts/search?q=thermal%20conductivity" title=" thermal conductivity"> thermal conductivity</a>, <a href="https://publications.waset.org/abstracts/search?q=thermal%20diffusivity" title=" thermal diffusivity"> thermal diffusivity</a>, <a href="https://publications.waset.org/abstracts/search?q=thermal%20analysis" title=" thermal analysis"> thermal analysis</a>, <a href="https://publications.waset.org/abstracts/search?q=electro-ceramics" title=" electro-ceramics"> electro-ceramics</a>, <a href="https://publications.waset.org/abstracts/search?q=firing" title=" firing"> firing</a> </p> <a href="https://publications.waset.org/abstracts/8438/using-the-transient-plane-source-method-for-measuring-thermal-parameters-of-electroceramics" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/8438.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">489</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">21884</span> Chemical Functionalization of Graphene Oxide for Improving Mechanical and Thermal Properties of Polyurethane Composites</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Qifei%20Jing">Qifei Jing</a>, <a href="https://publications.waset.org/abstracts/search?q=Vadim%20V.%20Silberschmidt"> Vadim V. Silberschmidt</a>, <a href="https://publications.waset.org/abstracts/search?q=Lin%20Li"> Lin Li</a>, <a href="https://publications.waset.org/abstracts/search?q=ZhiLi%20Dong"> ZhiLi Dong</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Graphene oxide (GO) was chemically functionalized to prepare polyurethane (PU) composites with improved mechanical and thermal properties. In order to achieve a well exfoliated and stable GO suspension in an organic solvent (dimethylformamide, DMF), 4, 4′- methylenebis(phenyl isocyanate) and polycaprolactone diol, which were the two monomers for synthesizing PU, were selectively used to functionalize GO. The obtained functionalized GO (FGO) could form homogeneous dispersions in DMF solvent and the PU matrix, as well as provide a good compatibility with the PU matrix. The most efficient improvement of mechanical properties was achieved when 0.4 wt% FGO was added into the PU matrix, showing increases in the tensile stress, elongation at break and toughness by 34.2%, 27.6% and 64.5%, respectively, compared with those of PU. Regarding the thermal stability, PU filled with 1 wt% FGO showed the largest extent of improvement with T2% and T50% (the temperatures at which 2% and 50% weight-loss happened) 16 °C and 21 °C higher than those of PU, respectively. The significant improvement in both mechanical properties and thermal stability of FGO/PU composites should be attributed to the homogeneous dispersion of FGO in the PU matrix and strong interfacial interaction between them. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=composite" title="composite">composite</a>, <a href="https://publications.waset.org/abstracts/search?q=dispersion" title=" dispersion"> dispersion</a>, <a href="https://publications.waset.org/abstracts/search?q=graphene%20oxide" title=" graphene oxide"> graphene oxide</a>, <a href="https://publications.waset.org/abstracts/search?q=polyurethane" title=" polyurethane"> polyurethane</a> </p> <a href="https://publications.waset.org/abstracts/38464/chemical-functionalization-of-graphene-oxide-for-improving-mechanical-and-thermal-properties-of-polyurethane-composites" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/38464.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">263</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">21883</span> Ultrathin NaA Zeolite Membrane in Solvent Recovery: Preparation and Application </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Eng%20Toon%20Saw">Eng Toon Saw</a>, <a href="https://publications.waset.org/abstracts/search?q=Kun%20Liang%20Ang"> Kun Liang Ang</a>, <a href="https://publications.waset.org/abstracts/search?q=Wei%20He"> Wei He</a>, <a href="https://publications.waset.org/abstracts/search?q=Xuecheng%20Dong"> Xuecheng Dong</a>, <a href="https://publications.waset.org/abstracts/search?q=Seeram%20Ramakrishna"> Seeram Ramakrishna</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Solvent recovery process is receiving utmost attention in recent year due to the scarcity of natural resource and consciousness of circular economy in chemical and pharmaceutical manufacturing process. Solvent dehydration process is one of the important process to recover and to purify the solvent for reuse. Due to the complexity of solvent waste or wastewater effluent produced in pharmaceutical industry resulting the wastewater treatment process become complicated, thus an alternative solution is to recover the valuable solvent in solvent waste. To treat solvent waste and to upgrade solvent purity, membrane pervaporation process is shown to be a promising technology due to the energy intensive and low footprint advantages. Ceramic membrane is adopted as solvent dehydration membrane owing to the chemical and thermal stability properties as compared to polymeric membrane. NaA zeolite membrane is generally used as solvent dehydration process because of its narrow and distinct pore size and high hydrophilicity. NaA zeolite membrane has been mainly applied in alcohol dehydration in fermentation process. At this stage, the membrane performance exhibits high separation factor with low flux using tubular ceramic membrane. Thus, defect free and ultrathin NaA membrane should be developed to increase water flux. Herein, we report a simple preparation protocol to prepare ultrathin NaA zeolite membrane supported on tubular ceramic membrane by controlling the seed size synthesis, seeding methods and conditions, ceramic substrate surface pore size selection and secondary growth conditions. The microstructure and morphology of NaA zeolite membrane will be examined and reported. Moreover, the membrane separation performance and stability will also be reported in isopropanol dehydration, ketone dehydration and ester dehydration particularly for the application in pharmaceutical industry. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=ceramic%20membrane" title="ceramic membrane">ceramic membrane</a>, <a href="https://publications.waset.org/abstracts/search?q=NaA%20zeolite" title=" NaA zeolite"> NaA zeolite</a>, <a href="https://publications.waset.org/abstracts/search?q=pharmaceutical%20industry" title=" pharmaceutical industry"> pharmaceutical industry</a>, <a href="https://publications.waset.org/abstracts/search?q=solvent%20recovery" title=" solvent recovery"> solvent recovery</a> </p> <a href="https://publications.waset.org/abstracts/96273/ultrathin-naa-zeolite-membrane-in-solvent-recovery-preparation-and-application" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/96273.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">245</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">21882</span> Olefin and Paraffin Separation Using Simulations on Extractive Distillation</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Muhammad%20Naeem">Muhammad Naeem</a>, <a href="https://publications.waset.org/abstracts/search?q=Abdulrahman%20A.%20Al-Rabiah"> Abdulrahman A. Al-Rabiah</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Technical mixture of C4 containing 1-butene and n-butane are very close to each other with respect to their boiling points i.e. -6.3°C for 1-butene and -1°C for n-butane. Extractive distillation process is used for the separation of 1-butene from the existing mixture of C4. The solvent is the essential of extractive distillation, and an appropriate solvent shows an important role in the process economy of extractive distillation. Aspen Plus has been applied for the separation of these hydrocarbons as a simulator; moreover NRTL activity coefficient model was used in the simulation. This model indicated that the material balances in this separation process were accurate for several solvent flow rates. Mixture of acetonitrile and water used as a solvent and 99 % pure 1-butene was separated. This simulation proposed the ratio of the feed to solvent as 1 : 7.9 and 15 plates for the solvent recovery column, previously feed to solvent ratio was more than this and the proposed plates were 30, which can economize the separation process. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=extractive%20distillation" title="extractive distillation">extractive distillation</a>, <a href="https://publications.waset.org/abstracts/search?q=1-butene" title=" 1-butene"> 1-butene</a>, <a href="https://publications.waset.org/abstracts/search?q=Aspen%20Plus" title=" Aspen Plus"> Aspen Plus</a>, <a href="https://publications.waset.org/abstracts/search?q=ACN%20solvent" title=" ACN solvent "> ACN solvent </a> </p> <a href="https://publications.waset.org/abstracts/10500/olefin-and-paraffin-separation-using-simulations-on-extractive-distillation" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/10500.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">447</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">21881</span> The Mechanism Study of Degradative Solvent Extraction of Biomass by Liquid Membrane-Fourier Transform Infrared Spectroscopy</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=W.%20Ketren">W. Ketren</a>, <a href="https://publications.waset.org/abstracts/search?q=J.%20Wannapeera"> J. Wannapeera</a>, <a href="https://publications.waset.org/abstracts/search?q=Z.%20Heishun"> Z. Heishun</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20Ryuichi"> A. Ryuichi</a>, <a href="https://publications.waset.org/abstracts/search?q=K.%20Toshiteru"> K. Toshiteru</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Kouichi"> M. Kouichi</a>, <a href="https://publications.waset.org/abstracts/search?q=O.%20Hideaki"> O. Hideaki</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Degradative solvent extraction is the method developed for biomass upgrading by dewatering and fractionation of biomass under the mild condition. However, the conversion mechanism of the degradative solvent extraction method has not been fully understood so far. The rice straw was treated in 1-methylnaphthalene (1-MN) at a different solvent-treatment temperature varied from 250 to 350 <sup>o</sup>C with the residence time for 60 min. The liquid membrane-Fourier Transform Infrared Spectroscopy (FTIR) technique is applied to study the processing mechanism in-depth without separation of the solvent. It has been found that the strength of the oxygen-hydrogen stretching (3600-3100 cm<sup>-1</sup>) decreased slightly with increasing temperature in the range of 300-350 <sup>o</sup>C. The decrease of the hydroxyl group in the solvent soluble suggested dehydration reaction taking place between 300 and 350 <sup>o</sup>C. FTIR spectra in the carbonyl stretching region (1800-1600 cm<sup>-1</sup>) revealed the presence of esters groups, carboxylic acid and ketonic groups in the solvent-soluble of biomass. The carboxylic acid increased in the range of 200 to 250<sup> o</sup>C and then decreased. The prevailing of aromatic groups showed that the aromatization took place during extraction at above 250 <sup>o</sup>C. From 300 to 350 <sup>o</sup>C, the carbonyl functional groups in the solvent-soluble noticeably decreased. The removal of the carboxylic acid and the decrease of esters into the form of carbon dioxide indicated that the decarboxylation reaction occurred during the extraction process. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biomass%20waste" title="biomass waste">biomass waste</a>, <a href="https://publications.waset.org/abstracts/search?q=degradative%20solvent%20extraction" title=" degradative solvent extraction"> degradative solvent extraction</a>, <a href="https://publications.waset.org/abstracts/search?q=mechanism" title=" mechanism"> mechanism</a>, <a href="https://publications.waset.org/abstracts/search?q=upgrading" title=" upgrading"> upgrading</a> </p> <a href="https://publications.waset.org/abstracts/79176/the-mechanism-study-of-degradative-solvent-extraction-of-biomass-by-liquid-membrane-fourier-transform-infrared-spectroscopy" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/79176.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">285</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">21880</span> Process Simulation of 1-Butene Separation from C4 Mixture by Extractive Distillation</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Muhammad%20Naeem">Muhammad Naeem</a>, <a href="https://publications.waset.org/abstracts/search?q=Abdulrahman%20A.%20Al-Rabiah"> Abdulrahman A. Al-Rabiah</a>, <a href="https://publications.waset.org/abstracts/search?q=Wasif%20Mughees"> Wasif Mughees</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Technical mixture of C4 containing 1-butene and n-butane are very close to each other with regard to their boiling points i.e. -6.3°C for 1-butene and -1°C for n-butane. Extractive distillation process is used for the separation of 1-butene from the existing mixture of C4. The solvent is the essential of extractive distillation, and an appropriate solvent plays an important role in the process economy of extractive distillation. Aspen Plus has been applied for the separation of these hydrocarbons as a simulator. Moreover, NRTL activity coefficient model was used in the simulation. This model indicated that the material balances in this separation process were accurate for several solvent flow rates. Mixture of acetonitrile and water used as a solvent and 99% pure 1-butene was separated. This simulation proposed the ratio of the feed to solvent as 1: 7.9 and 15 plates for the solvent recovery column. Previously feed to solvent ratio was more than this and the number of proposed plates were 30, which shows that the separation process can be economized. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=extractive%20distillation" title="extractive distillation">extractive distillation</a>, <a href="https://publications.waset.org/abstracts/search?q=1-butene" title=" 1-butene"> 1-butene</a>, <a href="https://publications.waset.org/abstracts/search?q=aspen%20plus" title=" aspen plus"> aspen plus</a>, <a href="https://publications.waset.org/abstracts/search?q=ACN%20solvent" title=" ACN solvent"> ACN solvent</a> </p> <a href="https://publications.waset.org/abstracts/5813/process-simulation-of-1-butene-separation-from-c4-mixture-by-extractive-distillation" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/5813.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">544</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">21879</span> Layer by Layer Coating of Zinc Oxide/Metal Organic Framework Nanocomposite on Ceramic Support for Solvent/Solvent Separation Using Pervaporation Method</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=S.%20A.%20A.%20Nabeela%20Nasreen">S. A. A. Nabeela Nasreen</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20Sundarrajan"> S. Sundarrajan</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20A.%20Syed%20Nizar"> S. A. Syed Nizar</a>, <a href="https://publications.waset.org/abstracts/search?q=Seeram%20Ramakrishna"> Seeram Ramakrishna</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Metal-organic frameworks (MOFs) have attracted considerable interest due to its diverse pore size tunability, fascinating topologies and extensive uses in fields such as catalysis, membrane separation, chemical sensing, etc. Zeolitic imidazolate frameworks (ZIFs) are a class of MOF with porous crystals containing extended three-dimensional structures of tetrahedral metal ions (e.g., Zn) bridged by Imidazolate (Im). Selected ZIFs are used to separate solvent/solvent mixtures. A layer by layer formation of the nanocomposite of Zinc oxide (ZnO) and ZIF on a ceramic support using a solvothermal method was engaged and tested for target solvent/solvent separation. Metal oxide layer was characterized by XRD, SEM, and TEM to confirm the smooth and continuous coating for the separation process. The chemical composition of ZIF films was studied by using X-Ray absorption near-edge structure (XANES) spectroscopy. The obtained ceramic tube with metal oxide and ZIF layer coating were tested for its packing density, thickness, distribution of seed layers and variation of permeation rate of solvent mixture (isopropyl alcohol (IPA)/methyl isobutyl ketone (MIBK). Pervaporation technique was used for the separation to achieve a high permeation rate with separation ratio of > 99.5% of the solvent mixture. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=metal%20oxide" title="metal oxide">metal oxide</a>, <a href="https://publications.waset.org/abstracts/search?q=membrane" title=" membrane"> membrane</a>, <a href="https://publications.waset.org/abstracts/search?q=pervaporation" title=" pervaporation"> pervaporation</a>, <a href="https://publications.waset.org/abstracts/search?q=solvothermal" title=" solvothermal"> solvothermal</a>, <a href="https://publications.waset.org/abstracts/search?q=ZIF" title=" ZIF"> ZIF</a> </p> <a href="https://publications.waset.org/abstracts/97314/layer-by-layer-coating-of-zinc-oxidemetal-organic-framework-nanocomposite-on-ceramic-support-for-solventsolvent-separation-using-pervaporation-method" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/97314.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">196</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">21878</span> Hydrometallurgical Treatment of Abu Ghalaga Ilmenite Ore</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=I.%20A.%20Ibrahim">I. A. Ibrahim</a>, <a href="https://publications.waset.org/abstracts/search?q=T.%20A.%20Elbarbary"> T. A. Elbarbary</a>, <a href="https://publications.waset.org/abstracts/search?q=N.%20Abdelaty"> N. Abdelaty</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20T.%20Kandil"> A. T. Kandil</a>, <a href="https://publications.waset.org/abstracts/search?q=H.%20K.%20Farhan"> H. K. Farhan</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The present work aims to study the leaching of Abu Ghalaga ilmenite ore by hydrochloric acid and simultaneous reduction by iron powder method to dissolve its titanium and iron contents. Iron content in the produced liquor is separated by solvent extraction using TBP as a solvent. All parameters affecting the efficiency of the dissolution process were separately studied including the acid concentration, solid/liquid ratio which controls the ilmenite/acid molar ratio, temperature, time and grain size. The optimum conditions at which maximum leaching occur are 30% HCl acid with a solid/liquid ratio of 1/30 at 80 °C for 4 h using ore ground to -350 mesh size. At the same time, all parameters affecting on solvent extraction and stripping of iron content from the produced liquor were studied. Results show that the best extraction is at solvent/solution 1/1 by shaking at 240 RPM for 45 minutes at 30 °C whereas best striping of iron at H₂O/solvent 2/1. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=ilmenite%20ore" title="ilmenite ore">ilmenite ore</a>, <a href="https://publications.waset.org/abstracts/search?q=leaching" title=" leaching"> leaching</a>, <a href="https://publications.waset.org/abstracts/search?q=titanium%20solvent%20extraction" title=" titanium solvent extraction"> titanium solvent extraction</a>, <a href="https://publications.waset.org/abstracts/search?q=Abu%20Ghalaga%20ilmenite%20ore" title=" Abu Ghalaga ilmenite ore"> Abu Ghalaga ilmenite ore</a> </p> <a href="https://publications.waset.org/abstracts/76625/hydrometallurgical-treatment-of-abu-ghalaga-ilmenite-ore" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/76625.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">290</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">21877</span> Solvent-Aided Dispersion of Tannic Acid to Enhance Flame Retardancy of Epoxy</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Matthew%20Korey">Matthew Korey</a>, <a href="https://publications.waset.org/abstracts/search?q=Jeffrey%20Youngblood"> Jeffrey Youngblood</a>, <a href="https://publications.waset.org/abstracts/search?q=John%20Howarter"> John Howarter</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Background and Significance: Tannic acid (TA) is a bio-based high molecular weight organic, aromatic molecule that has been found to increase thermal stability and flame retardancy of many polymer matrices when used as an additive. Although it is biologically sourced, TA is a pollutant in industrial wastewater streams, and there is a desire to find applications in which to downcycle this molecule after extraction from these streams. Additionally, epoxy thermosets have revolutionized many industries, but are too flammable to be used in many applications without additives which augment their flame retardancy (FR). Many flame retardants used in epoxy thermosets are synthesized from petroleum-based monomers leading to significant environmental impacts on the industrial scale. Many of these compounds also have significant impacts on human health. Various bio-based modifiers have been developed to improve the FR of the epoxy resin; however, increasing FR of the system without tradeoffs with other properties has proven challenging, especially for TA. Methodologies: In this work, TA was incorporated into the thermoset by use of solvent-exchange using methyl ethyl ketone, a co-solvent for TA, and epoxy resin. Samples were then characterized optically (UV-vis spectroscopy and optical microscopy), thermally (thermogravimetric analysis and differential scanning calorimetry), and for their flame retardancy (mass loss calorimetry). Major Findings: Compared to control samples, all samples were found to have increased thermal stability. Further, the addition of tannic acid to the polymer matrix by the use of solvent greatly increased the compatibility of the additive in epoxy thermosets. By using solvent-exchange, the highest loading level of TA found in literature was achieved in this work (40 wt%). Conclusions: The use of solvent-exchange shows promises for circumventing the limitations of TA in epoxy. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=sustainable" title="sustainable">sustainable</a>, <a href="https://publications.waset.org/abstracts/search?q=flame%20retardant" title=" flame retardant"> flame retardant</a>, <a href="https://publications.waset.org/abstracts/search?q=epoxy" title=" epoxy"> epoxy</a>, <a href="https://publications.waset.org/abstracts/search?q=tannic%20acid" title=" tannic acid"> tannic acid</a> </p> <a href="https://publications.waset.org/abstracts/116586/solvent-aided-dispersion-of-tannic-acid-to-enhance-flame-retardancy-of-epoxy" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/116586.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">130</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">21876</span> Split-Flow Method to Reduce Duty Required in Amine Gas Sweetening Units </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Abdallah%20Sofiane%20Berrouk">Abdallah Sofiane Berrouk</a>, <a href="https://publications.waset.org/abstracts/search?q=Dara%20Satyadileep"> Dara Satyadileep</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This paper investigates the feasibility of retrofitting a middle-east based commercial amine sweetening unit with a split-flow scheme which involves withdrawing a portion of partially stripped semi-lean solvent from the stripping column and re-injecting it in the absorption column to reduce the overall energy consumption of the unit. This method is comprehensively explored by performing parametric analysis of the split fraction of the semi-lean solvent using a kinetics based process simulator ProMax V 3.2. Re-boiler duty, condenser duty, solvent cooling and pumping loads are analysed as functions of a split fraction of the semi-lean solvent from the stripper. It is shown that the proposed method significantly reduces the overall energy consumption of the unit resulting in an annual savings of 325,000 USD. The thorough economic analysis is performed using Aspen Economic Evaluation V 8.4 to reveal that the retrofit scheme pays back the capital cost in less than eight years and is highly recommended for any commercial plant having suitable provisions for solvent inlet/withdrawal on the columns. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=split%20flow" title="split flow">split flow</a>, <a href="https://publications.waset.org/abstracts/search?q=Amine" title=" Amine"> Amine</a>, <a href="https://publications.waset.org/abstracts/search?q=gas%20processing" title=" gas processing"> gas processing</a>, <a href="https://publications.waset.org/abstracts/search?q=optimization" title=" optimization"> optimization</a> </p> <a href="https://publications.waset.org/abstracts/48530/split-flow-method-to-reduce-duty-required-in-amine-gas-sweetening-units" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/48530.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">329</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">21875</span> Thermal and Mechanical Properties of Powder Injection Molded Alumina Nano-Powder</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mostafa%20Rezaee%20Saraji">Mostafa Rezaee Saraji</a>, <a href="https://publications.waset.org/abstracts/search?q=Ali%20Keshavarz%20Panahi"> Ali Keshavarz Panahi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this work, the processing steps for producing alumina parts using powder injection molding (PIM) technique and nano-powder were investigated and the thermal conductivity and flexural strength of samples were determined as a function of sintering temperature and holding time. In the first step, the feedstock with 58 vol. % of alumina nano-powder with average particle size of 100nm was prepared using Extrumixing method to obtain appropriate homogeneity. This feedstock was injection molded into the two cavity mold with rectangular shape. After injection molding step, thermal and solvent debinding methods were used for debinding of molded samples and then these debinded samples were sintered in different sintering temperatures and holding times. From the results, it was found that the flexural strength and thermal conductivity of samples increased by increasing sintering temperature and holding time; in sintering temperature of 1600ºC and holding time of 5h, the flexural strength and thermal conductivity of sintered samples reached to maximum values of 488MPa and 40.8 W/mK, respectively. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=alumina%20nano-powder" title="alumina nano-powder">alumina nano-powder</a>, <a href="https://publications.waset.org/abstracts/search?q=thermal%20conductivity" title=" thermal conductivity"> thermal conductivity</a>, <a href="https://publications.waset.org/abstracts/search?q=flexural%20strength" title=" flexural strength"> flexural strength</a>, <a href="https://publications.waset.org/abstracts/search?q=powder%20injection%20molding" title=" powder injection molding"> powder injection molding</a> </p> <a href="https://publications.waset.org/abstracts/41809/thermal-and-mechanical-properties-of-powder-injection-molded-alumina-nano-powder" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/41809.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">329</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">21874</span> Typical Characteristics and Compositions of Solvent System in Application of Maceration Technology to Isolate Antioxidative Activated Extract of Natural Products</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Yohanes%20Buang">Yohanes Buang</a>, <a href="https://publications.waset.org/abstracts/search?q=Suwari"> Suwari</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Increasing interest of society in use and creation of herbal medicines has encouraged scientists/researchers to establish an ideal method to produce the best quality and quantity of pharmaceutical extracts. To have highest the antioxidative extracts, the method used must be at optimum conditions. Hence, the best method is not only able to provide highest quantity and quality of the isolated pharmaceutical extracts but also it has to be easy to do, simple, fast, and cheap. The characterization of solvents in maceration technique, in present study, involved various variables influencing quantity and quality of the pharmaceutical extracts, such as solvent’s optimum acidity-alkalinity (pH), temperature, concentration, and contact time. The shifting polarity of the solvent by combinations of water with ethanol (70:30) and (50:50) were also performed to completely record the best solvent system in application of maceration technology. Among those three solvents threated within Myrmecodia pendens, as a model of natural product, the results showed that water solvent system with conditions of alkalinity pH, optimum temperature, concentration, and contact time, is the best system to perform the maceration in order to have the highest isolated antioxidative activated extracts. The optimum conditions of the water solvent are at the alkalinity pH 9 up, 30 mg/mL of concentration, 40 min of contact time, 100 °C of temperature, and no ethanol used to replace parts of the water solvent. The present study strongly recommended the best conditions of solvent system to isolate the pharmaceutical extracts of natural products in application of the maceration technology. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=extracts" title="extracts">extracts</a>, <a href="https://publications.waset.org/abstracts/search?q=herbal%20medicine" title=" herbal medicine"> herbal medicine</a>, <a href="https://publications.waset.org/abstracts/search?q=natural%20product" title=" natural product"> natural product</a>, <a href="https://publications.waset.org/abstracts/search?q=maceration%20technique" title=" maceration technique"> maceration technique</a> </p> <a href="https://publications.waset.org/abstracts/48651/typical-characteristics-and-compositions-of-solvent-system-in-application-of-maceration-technology-to-isolate-antioxidative-activated-extract-of-natural-products" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/48651.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">299</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">21873</span> Extraction of Natural Colorant from the Flowers of Flame of Forest Using Ultrasound</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Sunny%20Arora">Sunny Arora</a>, <a href="https://publications.waset.org/abstracts/search?q=Meghal%20A.%20Desai"> Meghal A. Desai</a> </p> <p class="card-text"><strong>Abstract:</strong></p> An impetus towards green consumerism and implementation of sustainable techniques, consumption of natural products and utilization of environment friendly techniques have gained accelerated acceptance. Butein, a natural colorant, has many medicinal properties apart from its use in dyeing industries. Extraction of butein from the flowers of flame of forest was carried out using ultrasonication bath. Solid loading (2-6 g), extraction time (30-50 min), volume of solvent (30-50 mL) and types of solvent (methanol, ethanol and water) have been studied to maximize the yield of butein using the Taguchi method. The highest yield of butein 4.67% (w/w) was obtained using 4 g of plant material, 40 min of extraction time and 30 mL volume of methanol as a solvent. The present method provided a greater reduction in extraction time compared to the conventional method of extraction. Hence, the outcome of the present investigation could further be utilized to develop the method at a higher scale. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=butein" title="butein">butein</a>, <a href="https://publications.waset.org/abstracts/search?q=flowers%20of%20Flame%20of%20the%20Forest" title=" flowers of Flame of the Forest"> flowers of Flame of the Forest</a>, <a href="https://publications.waset.org/abstracts/search?q=Taguchi%20method" title=" Taguchi method"> Taguchi method</a>, <a href="https://publications.waset.org/abstracts/search?q=ultrasonic%20bath" title=" ultrasonic bath"> ultrasonic bath</a> </p> <a href="https://publications.waset.org/abstracts/79692/extraction-of-natural-colorant-from-the-flowers-of-flame-of-forest-using-ultrasound" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/79692.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">475</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">21872</span> Microwave Accelerated Simultaneous Distillation –Extraction: Preparative Recovery of Volatiles from Food Products</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ferhat%20Mohamed">Ferhat Mohamed</a>, <a href="https://publications.waset.org/abstracts/search?q=Boukhatem%20Mohamed%20Nadjib"> Boukhatem Mohamed Nadjib</a>, <a href="https://publications.waset.org/abstracts/search?q=Chemat%20Farid"> Chemat Farid</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Simultaneous distillation–extraction (SDE) is routinely used by analysts for sample preparation prior to gas chromatography analysis. In this work, a new process design and operation for microwave assisted simultaneous distillation – solvent extraction (MW-SDE) of volatile compounds was developed. Using the proposed method, isolation, extraction and concentration of volatile compounds can be carried out in a single step. To demonstrate its feasibility, MW-SDE was compared with the conventional technique, Simultaneous distillation–extraction (SDE), for gas chromatography-mass spectrometry (GC-MS) analysis of volatile compounds in a fresh orange juice and a dry spice “carvi seeds”. SDE method required long time (3 h) to isolate the volatile compounds, and large amount of organic solvent (200 mL of hexane) for further extraction, while MW-SDE needed little time (only 30 min) to prepare sample, and less amount of organic solvent (10 mL of hexane). These results show that MW-SDE–GC-MS is a simple, rapid and solvent-less method for determination of volatile compounds from aromatic plants. <p class="card-text"><strong>Keywords:</strong> <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=extraction" title=" extraction"> extraction</a>, <a href="https://publications.waset.org/abstracts/search?q=distillation" title=" distillation"> distillation</a>, <a href="https://publications.waset.org/abstracts/search?q=carvi%20seeds" title=" carvi seeds"> carvi seeds</a> </p> <a href="https://publications.waset.org/abstracts/30977/microwave-accelerated-simultaneous-distillation-extraction-preparative-recovery-of-volatiles-from-food-products" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/30977.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">560</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">21871</span> Thermo-Mechanical Characterization of MWCNTs-Modified Epoxy Resin</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=M.%20Dehghan">M. Dehghan</a>, <a href="https://publications.waset.org/abstracts/search?q=R.%20Al-Mahaidi"> R. Al-Mahaidi</a>, <a href="https://publications.waset.org/abstracts/search?q=I.%20Sbarski"> I. Sbarski</a> </p> <p class="card-text"><strong>Abstract:</strong></p> An industrial epoxy adhesive used in Carbon Fiber Reinforced Polymer (CFRP)-strengthening systems was modified by dispersing multi-walled carbon nanotubes (MWCNTs). Nanocomposites were fabricated using solvent-assisted dispersion method and ultrasonic mixing. Thermogravimetric analysis (TGA), dynamic mechanical analysis (DMA) and tensile tests were conducted to study the effect of nanotubes dispersion on the thermal and mechanical properties of the epoxy composite. Experimental results showed a substantial enhancement in the decomposition temperature and tensile properties of epoxy composite, while, the glass transition temperature (Tg) was slightly reduced due to the solvent effect. The morphology of the epoxy nanocomposites was investigated by SEM. It was proved that using solvent improves the nanotubes dispersion. However, at contents higher than 2 wt. %, nanotubes started to re-bundle in the epoxy matrix which negatively affected the final properties of epoxy composite. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=carbon%20fiber%20reinforced%20polymer" title="carbon fiber reinforced polymer">carbon fiber reinforced polymer</a>, <a href="https://publications.waset.org/abstracts/search?q=epoxy" title=" epoxy"> epoxy</a>, <a href="https://publications.waset.org/abstracts/search?q=multi-walled%20carbon%20nanotube" title=" multi-walled carbon nanotube"> multi-walled carbon nanotube</a>, <a href="https://publications.waset.org/abstracts/search?q=DMA" title=" DMA"> DMA</a>, <a href="https://publications.waset.org/abstracts/search?q=glass%20transition%20temperature" title=" glass transition temperature"> glass transition temperature</a> </p> <a href="https://publications.waset.org/abstracts/2485/thermo-mechanical-characterization-of-mwcnts-modified-epoxy-resin" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/2485.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">343</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">21870</span> Solvent Extraction and Spectrophotometric Determination of Palladium(II) Using P-Methylphenyl Thiourea as a Complexing Agent</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Shashikant%20R.%20Kuchekar">Shashikant R. Kuchekar</a>, <a href="https://publications.waset.org/abstracts/search?q=Somnath%20D.%20Bhumkar"> Somnath D. Bhumkar</a>, <a href="https://publications.waset.org/abstracts/search?q=Haribhau%20R.%20Aher"> Haribhau R. Aher</a>, <a href="https://publications.waset.org/abstracts/search?q=Bhaskar%20H.%20Zaware"> Bhaskar H. Zaware</a>, <a href="https://publications.waset.org/abstracts/search?q=Ponnadurai%20Ramasami"> Ponnadurai Ramasami</a> </p> <p class="card-text"><strong>Abstract:</strong></p> A precise, sensitive, rapid and selective method for the solvent extraction, spectrophotometric determination of palladium(II) using para-methylphenyl thiourea (PMPT) as an extractant is developed. Palladium(II) forms yellow colored complex with PMPT which shows an absorption maximum at 300 nm. The colored complex obeys Beer’s law up to 7.0 µg ml<sup>-1</sup> of palladium. The molar absorptivity and Sandell’s sensitivity were found to be 8.486 x 10<sup>3</sup> l mol<sup>-1</sup>cm<sup>-1</sup> and 0.0125 μg cm<sup>-2 </sup>respectively. The optimum conditions for the extraction and determination of palladium have been established by monitoring the various experimental parameters. The precision of the method has been evaluated and the relative standard deviation has been found to be less than 0.53%. The proposed method is free from interference from large number of foreign ions. The method has been successfully applied for the determination of palladium from alloy, synthetic mixtures corresponding to alloy samples. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=solvent%20extraction" title="solvent extraction">solvent extraction</a>, <a href="https://publications.waset.org/abstracts/search?q=PMPT" title=" PMPT"> PMPT</a>, <a href="https://publications.waset.org/abstracts/search?q=Palladium%20%28II%29" title=" Palladium (II)"> Palladium (II)</a>, <a href="https://publications.waset.org/abstracts/search?q=spectrophotometry" title=" spectrophotometry"> spectrophotometry</a> </p> <a href="https://publications.waset.org/abstracts/68759/solvent-extraction-and-spectrophotometric-determination-of-palladiumii-using-p-methylphenyl-thiourea-as-a-complexing-agent" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/68759.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">461</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">21869</span> Electrodeposition of NiO Films from Organic Solvent-Based Electrolytic Solutions for Solar Cell Application </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Thierry%20Pauport%C3%A9">Thierry Pauporté</a>, <a href="https://publications.waset.org/abstracts/search?q=Sana%20Koussi"> Sana Koussi</a>, <a href="https://publications.waset.org/abstracts/search?q=Fabrice%20Odobel"> Fabrice Odobel</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The preparation of semiconductor oxide layers and structures by soft techniques is an important field of research. Higher performances are expected from the optimizing of the oxide films and then use of new methods of preparation for a better control of their chemical, morphological, electrical and optical properties. We present the preparation of NiO by electrodeposition from pure polar aprotic medium and mixtures with water. The effect of the solvent, of the electrochemical deposition parameters and post-deposition annealing treatment on the structural, morphological and optical properties of the films is investigated. We remarkably show that the solvent is inserted in the deposited layer and act as a blowing agent, giving rise to mesoporous films after elimination by thermal annealing. These layers of p-type oxide have been successfully used, after sensitization by a dye, in p-type dye-sensitized solar cells. The effects of the solvent on the layer properties and the application of these layers in p-type dye-sensitized solar cells are described. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=NiO" title="NiO">NiO</a>, <a href="https://publications.waset.org/abstracts/search?q=layer" title=" layer"> layer</a>, <a href="https://publications.waset.org/abstracts/search?q=p-type%20sensitized%20solar%20cells" title=" p-type sensitized solar cells"> p-type sensitized solar cells</a>, <a href="https://publications.waset.org/abstracts/search?q=electrodeposition" title=" electrodeposition"> electrodeposition</a> </p> <a href="https://publications.waset.org/abstracts/66597/electrodeposition-of-nio-films-from-organic-solvent-based-electrolytic-solutions-for-solar-cell-application" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/66597.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">297</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">21868</span> Comparison of Finite-Element and IEC Methods for Cable Thermal Analysis under Various Operating Environments</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=M.%20S.%20Baazzim">M. S. Baazzim</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20S.%20Al-Saud"> M. S. Al-Saud</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20A.%20El-Kady"> M. A. El-Kady</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this paper, steady-state ampacity (current carrying capacity) evaluation of underground power cable system by using analytical and numerical methods for different conditions (depth of cable, spacing between phases, soil thermal resistivity, ambient temperature, wind speed), for two system voltage level were used 132 and 380 kV. The analytical method or traditional method that was used is based on the thermal analysis method developed by Neher-McGrath and further enhanced by International Electrotechnical Commission (IEC) and published in standard IEC 60287. The numerical method that was used is finite element method and it was recourse commercial software based on finite element method. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=cable%20ampacity" title="cable ampacity">cable ampacity</a>, <a href="https://publications.waset.org/abstracts/search?q=finite%20element%20method" title=" finite element method"> finite element method</a>, <a href="https://publications.waset.org/abstracts/search?q=underground%20cable" title=" underground cable"> underground cable</a>, <a href="https://publications.waset.org/abstracts/search?q=thermal%20rating" title=" thermal rating"> thermal rating</a> </p> <a href="https://publications.waset.org/abstracts/6273/comparison-of-finite-element-and-iec-methods-for-cable-thermal-analysis-under-various-operating-environments" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/6273.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">21867</span> Determination of Antioxidant Activities of Sumac (Rhus Coriaria) Extracts with Different Solvents</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=F.%20T.%20Senberber">F. T. Senberber</a>, <a href="https://publications.waset.org/abstracts/search?q=N.%20Tugrul"> N. Tugrul</a>, <a href="https://publications.waset.org/abstracts/search?q=E.%20Moroydor%20Derun"> E. Moroydor Derun</a> </p> <p class="card-text"><strong>Abstract:</strong></p> As a nutraceutical, sumac (Rhus Coriaria) was extracted by using different solvents of methanol, ethanol, and water. The DPPH (2,2-diphenyl-1-picryl-hydrazyl-hydrate) method of free radical scavenging capacity was used to determine the effects of solvent on antioxidant activities of the plant. The total phenolic content was studied by The Folin Ciocalteu Reagent method. The antioxidant activities of extracts exhibit minor changes in different solvents and varied in the range of 84.3–86.4 %. The total phenolic contents are affected by the selected solvent. The highest total phenolic content was determined at the liquid phase of water and it was estimated as 26.3 mg/g in gallic acid. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=DPPH" title="DPPH">DPPH</a>, <a href="https://publications.waset.org/abstracts/search?q=solvent" title=" solvent"> solvent</a>, <a href="https://publications.waset.org/abstracts/search?q=sumac" title=" sumac"> sumac</a>, <a href="https://publications.waset.org/abstracts/search?q=total%20phenolic%20content" title=" total phenolic content"> total phenolic content</a> </p> <a href="https://publications.waset.org/abstracts/124315/determination-of-antioxidant-activities-of-sumac-rhus-coriaria-extracts-with-different-solvents" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/124315.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">153</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">21866</span> Impact of Flavor on Food Product Quality, A Case Study of Vanillin Stability during Biscuit Preparation</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=N.%20Yang">N. Yang</a>, <a href="https://publications.waset.org/abstracts/search?q=R.%20Linforth"> R. Linforth</a>, <a href="https://publications.waset.org/abstracts/search?q=I.%20Fisk"> I. Fisk</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The influence of food processing and choice of flavour solvent was investigated using biscuits prepared with vanillin flavour as an example. Powder vanillin either was added directly into the dough or dissolved into flavour solvent then mixed into the dough. The impact of two commonly used flavour solvents on food quality was compared: propylene glycol (PG) or triacetin (TA). The analytical approach for vanillin detection was developed by chromatography (HPLC-PDA), and the standard extraction method for vanillin was also established. The results indicated the impact of solvent choice on vanillin level during biscuit preparation. After baking, TA as a more heat resistant solvent retained more vanillin than PG, so TA is a better solvent for products that undergo a heating process. The results also illustrated the impact of mixing and baking on vanillin stability in the matrices. The average loss of vanillin was 33% during mixing and 13% during baking, which indicated that the binding of vanillin to fat or flour before baking might cause larger loss than evaporation loss during baking. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biscuit" title="biscuit">biscuit</a>, <a href="https://publications.waset.org/abstracts/search?q=flavour%20stability" title=" flavour stability"> flavour stability</a>, <a href="https://publications.waset.org/abstracts/search?q=food%20quality" title=" food quality"> food quality</a>, <a href="https://publications.waset.org/abstracts/search?q=vanillin" title=" vanillin"> vanillin</a> </p> <a href="https://publications.waset.org/abstracts/25487/impact-of-flavor-on-food-product-quality-a-case-study-of-vanillin-stability-during-biscuit-preparation" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/25487.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">508</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">21865</span> Solvent Extraction, Spectrophotometric Determination of Antimony(III) from Real Samples and Synthetic Mixtures Using O-Methylphenyl Thiourea as a Sensitive Reagent</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Shashikant%20R.%20Kuchekar">Shashikant R. Kuchekar</a>, <a href="https://publications.waset.org/abstracts/search?q=Shivaji%20D.%20Pulate"> Shivaji D. Pulate</a>, <a href="https://publications.waset.org/abstracts/search?q=Vishwas%20B.%20Gaikwad"> Vishwas B. Gaikwad</a> </p> <p class="card-text"><strong>Abstract:</strong></p> A simple and selective method is developed for solvent extraction spectrophotometric determination of antimony(III) using O-Methylphenyl Thiourea (OMPT) as a sensitive chromogenic chelating agent. The basis of proposed method is formation of antimony(III)-OMPT complex was extracted with 0.0025 M OMPT in chloroform from aqueous solution of antimony(III) in 1.0 M perchloric acid. The absorbance of this complex was measured at 297 nm against reagent blank. Beer’s law was obeyed up to 15µg mL-1 of antimony(III). The Molar absorptivity and Sandell’s sensitivity of the antimony(III)-OMPT complex in chloroform are 16.6730 × 103 L mol-1 cm-1 and 0.00730282 µg cm-2 respectively. The stoichiometry of antimony(III)-OMPT complex was established from slope ratio method, mole ratio method and Job’s continuous variation method was 1:2. The complex was stable for more than 48 h. The interfering effect of various foreign ions was studied and suitable masking agents are used wherever necessary to enhance selectivity of the method. The proposed method is successfully applied for determination of antimony(III) from real samples alloy and synthetic mixtures. Repetition of the method was checked by finding relative standard deviation (RSD) for 10 determinations which was 0.42%. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=solvent%20extraction" title="solvent extraction">solvent extraction</a>, <a href="https://publications.waset.org/abstracts/search?q=antimony" title=" antimony"> antimony</a>, <a href="https://publications.waset.org/abstracts/search?q=spectrophotometry" title=" spectrophotometry"> spectrophotometry</a>, <a href="https://publications.waset.org/abstracts/search?q=real%20sample%20analysis" title=" real sample analysis"> real sample analysis</a> </p> <a href="https://publications.waset.org/abstracts/68993/solvent-extraction-spectrophotometric-determination-of-antimonyiii-from-real-samples-and-synthetic-mixtures-using-o-methylphenyl-thiourea-as-a-sensitive-reagent" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/68993.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">332</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">21864</span> Rational Probabilistic Method for Calculating Thermal Cracking Risk of Mass Concrete Structures</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Naoyuki%20Sugihashi">Naoyuki Sugihashi</a>, <a href="https://publications.waset.org/abstracts/search?q=Toshiharu%20Kishi"> Toshiharu Kishi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The probability of occurrence of thermal cracks in mass concrete in Japan is evaluated by the cracking probability diagram that represents the relationship between the thermal cracking index and the probability of occurrence of cracks in the actual structure. In this paper, we propose a method to directly calculate the cracking probability, following a probabilistic theory by modeling the variance of tensile stress and tensile strength. In this method, the relationship between the variance of tensile stress and tensile strength, the thermal cracking index, and the cracking probability are formulated and presented. In addition, standard deviation of tensile stress and tensile strength was identified, and the method of calculating cracking probability in a general construction controlled environment was also demonstrated. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=thermal%20crack%20control" title="thermal crack control">thermal crack control</a>, <a href="https://publications.waset.org/abstracts/search?q=mass%20concrete" title=" mass concrete"> mass concrete</a>, <a href="https://publications.waset.org/abstracts/search?q=thermal%20cracking%20probability" title=" thermal cracking probability"> thermal cracking probability</a>, <a href="https://publications.waset.org/abstracts/search?q=durability%20of%20concrete" title=" durability of concrete"> durability of concrete</a>, <a href="https://publications.waset.org/abstracts/search?q=calculating%20method%20of%20cracking%20probability" title=" calculating method of cracking probability"> calculating method of cracking probability</a> </p> <a href="https://publications.waset.org/abstracts/74943/rational-probabilistic-method-for-calculating-thermal-cracking-risk-of-mass-concrete-structures" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/74943.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">346</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">21863</span> Optimized Simultaneous Determination of Theobromine and Caffeine in Fermented and Unfermented Cacao Beans and in Cocoa Products Using Step Gradient Solvent System in Reverse Phase HPLC</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ian%20Marc%20G.%20Cabugsa">Ian Marc G. Cabugsa</a>, <a href="https://publications.waset.org/abstracts/search?q=Kim%20Ryan%20A.%20Won"> Kim Ryan A. Won</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Fast, reliable and simultaneous HPLC analysis of theobromine and caffeine in cacao and cocoa products was optimized in this study. The samples tested were raw, fermented, and roasted cacao beans as well as commercially available cocoa products. The HPLC analysis was carried out using step gradient solvent system with acetonitrile and water buffered with H3PO4 as the mobile phase. The HPLC system was optimized using 273 nm wavelength at 35 °C for the column temperature with a flow rate of 1.0 mL/min. Using this method, the theobromine percent recovery mean, Limit of Detection (LOD) and Limit of Quantification (LOQ) is 118.68(±3.38)%, 0.727 and 1.05 respectively. The percent recovery mean, LOD and LOQ for caffeine is 105.53(±3.25)%, 2.42 and 3.50 respectively. The inter-day and intra-day precision for theobromine is 4.31% and 4.48% respectively, while 7.02% and 7.03% was for caffeine respectively. Compared to the standard method in AOAC using methanol in isocratic solvent system, the results of the study produced lesser chromatogram noise with emphasis on theobromine and caffeine. The method is readily usable for cacao and cocoa substances analyses using HPLC with step gradient capability. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=cacao" title="cacao">cacao</a>, <a href="https://publications.waset.org/abstracts/search?q=caffeine" title=" caffeine"> caffeine</a>, <a href="https://publications.waset.org/abstracts/search?q=HPLC" title=" HPLC"> HPLC</a>, <a href="https://publications.waset.org/abstracts/search?q=step%20gradient%20solvent%20system" title=" step gradient solvent system"> step gradient solvent system</a>, <a href="https://publications.waset.org/abstracts/search?q=theobromine" title=" theobromine"> theobromine</a> </p> <a href="https://publications.waset.org/abstracts/43155/optimized-simultaneous-determination-of-theobromine-and-caffeine-in-fermented-and-unfermented-cacao-beans-and-in-cocoa-products-using-step-gradient-solvent-system-in-reverse-phase-hplc" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/43155.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">281</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">21862</span> Stability-Indicating High-Performance Thin-Layer Chromatography Method for Estimation of Naftopidil</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=P.%20S.%20Jain">P. S. Jain</a>, <a href="https://publications.waset.org/abstracts/search?q=K.%20D.%20Bobade"> K. D. Bobade</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20J.%20Surana"> S. J. Surana</a> </p> <p class="card-text"><strong>Abstract:</strong></p> A simple, selective, precise and Stability-indicating High-performance thin-layer chromatographic method for analysis of Naftopidil both in a bulk and in pharmaceutical formulation has been developed and validated. The method employed, HPTLC aluminium plates precoated with silica gel as the stationary phase. The solvent system consisted of hexane: ethyl acetate: glacial acetic acid (4:4:2 v/v). The system was found to give compact spot for Naftopidil (Rf value of 0.43±0.02). Densitometric analysis of Naftopidil was carried out in the absorbance mode at 253 nm. The linear regression analysis data for the calibration plots showed good linear relationship with r2=0.999±0.0001 with respect to peak area in the concentration range 200-1200 ng per spot. The method was validated for precision, recovery and robustness. The limits of detection and quantification were 20.35 and 61.68 ng per spot, respectively. Naftopidil was subjected to acid and alkali hydrolysis, oxidation and thermal degradation. The drug undergoes degradation under acidic, basic, oxidation and thermal conditions. This indicates that the drug is susceptible to acid, base, oxidation and thermal conditions. The degraded product was well resolved from the pure drug with significantly different Rf value. Statistical analysis proves that the method is repeatable, selective and accurate for the estimation of investigated drug. The proposed developed HPTLC method can be applied for identification and quantitative determination of Naftopidil in bulk drug and pharmaceutical formulation. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=naftopidil" title="naftopidil">naftopidil</a>, <a href="https://publications.waset.org/abstracts/search?q=HPTLC" title=" HPTLC"> HPTLC</a>, <a href="https://publications.waset.org/abstracts/search?q=validation" title=" validation"> validation</a>, <a href="https://publications.waset.org/abstracts/search?q=stability" title=" stability"> stability</a>, <a href="https://publications.waset.org/abstracts/search?q=degradation" title=" degradation"> degradation</a> </p> <a href="https://publications.waset.org/abstracts/18308/stability-indicating-high-performance-thin-layer-chromatography-method-for-estimation-of-naftopidil" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/18308.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">400</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">21861</span> Purification of Zr from Zr-Hf Resources Using Crystallization in HF-HCl Solvent Mixture</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Kenichi%20Hirota">Kenichi Hirota</a>, <a href="https://publications.waset.org/abstracts/search?q=Jifeng%20Wang"> Jifeng Wang</a>, <a href="https://publications.waset.org/abstracts/search?q=Sadao%20Araki"> Sadao Araki</a>, <a href="https://publications.waset.org/abstracts/search?q=Koji%20Endo"> Koji Endo</a>, <a href="https://publications.waset.org/abstracts/search?q=Hideki%20Yamamoto"> Hideki Yamamoto</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Zirconium (Zr) has been used as a fuel cladding tube for nuclear reactors, because of the excellent corrosion resistance and the low adsorptive material for neutron. Generally speaking, the natural resource of Zr is often containing Hf that has similar properties. The content of Hf in the Zr resources is about 2~4 wt%. In the industrial use, the content of Hf in Zr resources should be lower than the 100 ppm. However, the separation of Zr and Hf is not so easy, because of similar chemical and physical properties such as melting point, boiling point and things. Solvent extraction method has been applied for the separation of Zr and Hf from Zr natural resources. This method can separate Hf with high efficiency (Hf < 100ppm), however, it needs much amount of organic solvents for solvent extraction and the cost of its disposal treatment is high. Therefore, we attached attention for the fractional crystallization. This separation method depends on the solubility difference of Zr and Hf in the solvent. In this work, hexafluorozirconate (hafnate) (K2Zr(Hf)F6) was used as model compound. Solubility of K2ZrF6 in water showed lower than that of K2HfF6. By repeating of this treatment, it is possible to purify Zr, practically. In this case, 16-18 times of recrystallization stages were needed for its high purification. The improvement of the crystallization process was carried out in this work. Water, hydrofluoric acid (HF) and hydrofluoric acid (HF) +hydrochloric acid (HCl) mixture were chosen as solvent for dissolution of Zr and Hf. In the experiment, 10g of K2ZrF6 was added to each solvent of 100mL. Each solution was heated for 1 hour at 353K. After 1h of this operation, they were cooled down till 293K, and were held for 5 hours at 273K. Concentration of Zr or Hf was measured using ICP analysis. It was found that Hf was separated from Zr-Hf mixed compound with high efficiency, when HF-HCl solution was used for solvent of crystallization. From the comparison of the particle size of each crystal by SEM, it was confirmed that the particle diameter of the crystal showed smaller size with decreasing of Hf content. This paper concerned with purification of Zr from Zr-Hf mixture using crystallization method. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=crystallization" title="crystallization">crystallization</a>, <a href="https://publications.waset.org/abstracts/search?q=zirconium" title=" zirconium"> zirconium</a>, <a href="https://publications.waset.org/abstracts/search?q=hafnium" title=" hafnium"> hafnium</a>, <a href="https://publications.waset.org/abstracts/search?q=separation" title=" separation"> separation</a> </p> <a href="https://publications.waset.org/abstracts/35531/purification-of-zr-from-zr-hf-resources-using-crystallization-in-hf-hcl-solvent-mixture" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/35531.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">437</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">21860</span> Improvement of Egyptian Vacuum Distillates by Solvent Dewaxing</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ehssan%20M.%20R.%20Nassef">Ehssan M. R. Nassef</a> </p> <p class="card-text"><strong>Abstract:</strong></p> De-waxing of vacuum distillates by using solvent was investigated in the present study. The present work deals with studying solvent dewaxing system which have been developed to give better dewaxing performance with respect to the important factors in the choice of solvents which are good solubility of oil in the solvent and low solubility of wax in the solvent. In this study, solvent dewaxing process using Methyl Ethyl Ketone (MEK) and toluene are used for Egyptian vacuum distillates using two types of distillates. The effect of varying the composition of(MEK to toluene) on the percent yield of the oil, percent of wax, pour point, refractive index at 20 and 70°C, viscosity at 40 and 100°C, viscosity index and specific gravity of the oil produced for the two types of distillates (I & II) were evaluated. In the present study, the operating conditions of solvent dewaxing using MEK toluene mixture achieved the best pour point at -15°C for distillate I at (1:1) solvent composition mixture. At the same ratio of MEK to toluene the best specific gravity of oil produced changed from 0.871 to 0.8802, with refractive index of 1.84. Percent yield of 65% for oil was obtained. The results for distillate II, of higher specific gravity, are comparatively higher than those for distillate I. The effect of temperature was also investigated and the best temperature was -20°C. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=dewaxing" title="dewaxing">dewaxing</a>, <a href="https://publications.waset.org/abstracts/search?q=solvent%20dewaxing" title=" solvent dewaxing"> solvent dewaxing</a>, <a href="https://publications.waset.org/abstracts/search?q=pour%20point" title=" pour point"> pour point</a>, <a href="https://publications.waset.org/abstracts/search?q=lubricating%20oil%20production" title=" lubricating oil production"> lubricating oil production</a>, <a href="https://publications.waset.org/abstracts/search?q=wax" title=" wax "> wax </a> </p> <a href="https://publications.waset.org/abstracts/22202/improvement-of-egyptian-vacuum-distillates-by-solvent-dewaxing" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/22202.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">532</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">21859</span> Investigation of Solvent Effect on Viscosity of Lubricant in Disposable Medical Devices</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hamed%20Bagheri">Hamed Bagheri</a>, <a href="https://publications.waset.org/abstracts/search?q=Seyd%20Javid%20Shariati"> Seyd Javid Shariati</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The effects of type and amount of solvent on lubricant which is used in disposable medical devices are investigated in this article. Two kinds of common solvent, n-Hexane and n-Heptane, are used. The mechanical behavior of syringe has shown that n-Heptane has better mixing ratio and also more effective spray process in the barrel of syringe than n-Hexane because of similar solubility parameter to silicon oil. The results revealed that movement of plunger in the barrel increases when pure silicone is used because non-uniform film is created on the surface of barrel, and also, it seems that the form of silicon is converted from oil to gel due to sterilization process. The results showed that the convenient mixing ratio of solvent/lubricant oil is 80/20. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=disposal%20medical%20devices" title="disposal medical devices">disposal medical devices</a>, <a href="https://publications.waset.org/abstracts/search?q=lubricant%20oil" title=" lubricant oil"> lubricant oil</a>, <a href="https://publications.waset.org/abstracts/search?q=solvent%20effect" title=" solvent effect"> solvent effect</a>, <a href="https://publications.waset.org/abstracts/search?q=solubility%20parameter" title=" solubility parameter"> solubility parameter</a> </p> <a href="https://publications.waset.org/abstracts/72192/investigation-of-solvent-effect-on-viscosity-of-lubricant-in-disposable-medical-devices" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/72192.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">231</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">21858</span> First Approach on Lycopene Extraction Using Limonene</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> Lycopene extraction with petroleum derivatives as solvents has caused safety, health, and environmental concerns everywhere. Thus, finding a safe alternative solvent will have a strong and positive impact on environments and general health of the world population. d-limonene from the orange peel was extracted through a steam distillation procedure followed by a deterpenation process and combining this achievement by using it as a solvent for extracting lycopene from tomato fruit as a substitute of dichloromethane. Lycopene content of fresh tomatoes was determined by high-performance liquid chromatography after extraction. Yields obtained for both extractions showed that yields of d-limonene’s extracts were almost equivalent to those obtained using dichloromethane. The proposed approach using a green solvent to perform extraction is useful and can be considered as a nice alternative to conventional petroleum solvent where toxicity for both operator and environment is reduced. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=alternative%20solvent" title="alternative solvent">alternative solvent</a>, <a href="https://publications.waset.org/abstracts/search?q=d-limonene" title=" d-limonene"> d-limonene</a>, <a href="https://publications.waset.org/abstracts/search?q=extraction" title=" extraction"> extraction</a>, <a href="https://publications.waset.org/abstracts/search?q=lycopene" title=" lycopene"> lycopene</a> </p> <a href="https://publications.waset.org/abstracts/51267/first-approach-on-lycopene-extraction-using-limonene" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/51267.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">413</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">21857</span> Magnetic Solvent Extraction Using Nanoparticles Coated by Oleic Acid</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Nat%C3%A1lia%20C.%20C.%20Lobato">Natália C. C. Lobato</a>, <a href="https://publications.waset.org/abstracts/search?q=%C3%82ngela%20M.%20Ferreira"> Ângela M. Ferreira</a>, <a href="https://publications.waset.org/abstracts/search?q=Marcelo%20B.%20Mansur"> Marcelo B. Mansur</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In solvent extraction operations, large sedimentation areas in the mixer-settler are required when the disengagement of the aqueous and the organic phases is slow and/or difficult. The use of a magnetic organic liquid (also known as ferrofluid), consisting of magnetite nanoparticles coated by oleic acid dispersed in the organic diluent, has proven successful to speed up phase disengagement. The method, however, has never been used industrially; therefore, the aim of this study is to raise its main limitations. Tests were carried out using a ferrofluid containing 30 g/l of magnetite dissolved in commercial aliphatic kerosene Exxsol D80. The efficiency of cobalt extraction ([Co] = 1 g/l) with 10% v/v Cyanex 272 (bis-2,4,4-trimethylpentyl phosphinic acid) at changing pH of the aqueous phase (2 to 7) was found unaffected in the conditions studied. However, the chemical resistance of the ferrofluid in contact with deionized water at changing acidity (from 10-7 to 2 mol/l) revealed that the nanoparticles are not resistant when contacted to aqueous solutions with a pH ≤ 2. Such result represents a serious limitation to the applicability of the method mainly to hydrometallurgical systems because solvent extraction operations are normally done in acid conditions, therefore more effective strategies to coat the particles are required. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=magnetic%20solvent%20extraction" title="magnetic solvent extraction">magnetic solvent extraction</a>, <a href="https://publications.waset.org/abstracts/search?q=oleic%20acid" title=" oleic acid"> oleic acid</a>, <a href="https://publications.waset.org/abstracts/search?q=magnetite%20nanoparticles" title=" magnetite nanoparticles"> magnetite nanoparticles</a>, <a href="https://publications.waset.org/abstracts/search?q=cyanex%20272" title=" cyanex 272"> cyanex 272</a> </p> <a href="https://publications.waset.org/abstracts/41603/magnetic-solvent-extraction-using-nanoparticles-coated-by-oleic-acid" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/41603.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">395</span> </span> </div> </div> <ul class="pagination"> <li class="page-item disabled"><span class="page-link">‹</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=solvent%20thermal%20method&page=2">2</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=solvent%20thermal%20method&page=3">3</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=solvent%20thermal%20method&page=4">4</a></li> <li class="page-item"><a class="page-link" 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