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thermogravimetric</title> <meta name="description" content="Search results for: thermogravimetric"> <meta name="keywords" content="thermogravimetric"> <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="thermogravimetric"> <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> 225</div> </div> </div> </div> <h1 class="mt-3 mb-3 text-center" style="font-size:1.6rem;">Search results for: thermogravimetric</h1> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">225</span> Co-Pyrolysis of Bituminous Coal with Peat by Thermogravimetric Analysis</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ceren%20Efe">Ceren Efe</a>, <a href="https://publications.waset.org/abstracts/search?q=Hale%20S%C3%BCt%C3%A7%C3%BC"> Hale Sütçü</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this study, the pyrolysis of bituminous coal, peat and their blends formed by mixing various ratios of them were examined by thermogravimetric analysis method. Thermogravimetric analyses of peat, bituminous coal and their blends in the proportions of 25 %, 50 % and 75 % were performed at heating rate of 10 °C/min and from the room temperature until to 800 °C temperature, in a nitrogen atmosphere of 100 ml/min. Kinetic parameters for the pyrolysis process were calculated using Coats&Redfern kinetic model. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=bituminous%20coal" title="bituminous coal">bituminous coal</a>, <a href="https://publications.waset.org/abstracts/search?q=peat" title=" peat"> peat</a>, <a href="https://publications.waset.org/abstracts/search?q=pyrolysis" title=" pyrolysis"> pyrolysis</a>, <a href="https://publications.waset.org/abstracts/search?q=thermogravimetric%20analysis" title=" thermogravimetric analysis"> thermogravimetric analysis</a>, <a href="https://publications.waset.org/abstracts/search?q=Coats%26Redfern" title=" Coats&Redfern"> Coats&Redfern</a> </p> <a href="https://publications.waset.org/abstracts/62239/co-pyrolysis-of-bituminous-coal-with-peat-by-thermogravimetric-analysis" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/62239.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">262</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">224</span> Pyrolysis and Combustion Kinetics of Palm Kernel Shell Using Thermogravimetric Analysis</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Kanit%20Manatura">Kanit Manatura</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The combustion and pyrolysis behavior of Palm Kernel Shell (PKS) were investigated in a thermogravimetric analyzer. A 10 mg sample of each biomass was heated from 30 °C to 800 °C at four heating rates (within 5, 10, 15 and 30 °C/min) in nitrogen and dry air flow of 20 ml/min instead of pyrolysis and combustion process respectively. During pyrolysis, thermal decomposition occurred on three different stages include dehydration, hemicellulose-cellulose and lignin decomposition on each temperature range. The TG/DTG curves showed the degradation behavior and the pyrolysis/combustion characteristics of the PKS samples which led to apply in thermogravimetric analysis. The kinetic factors including activation energy and pre-exponential factor were determined by the Coats-Redfern method. The obtained kinetic factors are used to simulate the thermal decomposition and compare with experimental data. Rising heating rate leads to shift the mass loss towards higher temperature. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=combustion" title="combustion">combustion</a>, <a href="https://publications.waset.org/abstracts/search?q=palm%20kernel%20shell" title=" palm kernel shell"> palm kernel shell</a>, <a href="https://publications.waset.org/abstracts/search?q=pyrolysis" title=" pyrolysis"> pyrolysis</a>, <a href="https://publications.waset.org/abstracts/search?q=thermogravimetric%20analyzer" title=" thermogravimetric analyzer"> thermogravimetric analyzer</a> </p> <a href="https://publications.waset.org/abstracts/84897/pyrolysis-and-combustion-kinetics-of-palm-kernel-shell-using-thermogravimetric-analysis" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/84897.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">228</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">223</span> Pyrolysis of Dursunbey Lignite and Pyrolysis Kinetics</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=H.%20S%C3%BCt%C3%A7%C3%BC">H. Sütçü</a>, <a href="https://publications.waset.org/abstracts/search?q=C.%20Efe"> C. Efe</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this study, pyrolysis characteristics of Dursunbey-Balıkesir lignite and its pyrolysis kinetics are examined. The pyrolysis experiments carried out at three different heating rates are performed by using thermogravimetric method. Kinetic parameters are calculated by Coats & Redfern kinetic model and the degree of pyrolysis process is determined for each of the heating rate. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=lignite" title="lignite">lignite</a>, <a href="https://publications.waset.org/abstracts/search?q=thermogravimetric%20analysis" title=" thermogravimetric analysis"> thermogravimetric analysis</a>, <a href="https://publications.waset.org/abstracts/search?q=pyrolysis" title=" pyrolysis"> pyrolysis</a>, <a href="https://publications.waset.org/abstracts/search?q=kinetics" title=" kinetics"> kinetics</a> </p> <a href="https://publications.waset.org/abstracts/61724/pyrolysis-of-dursunbey-lignite-and-pyrolysis-kinetics" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/61724.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">367</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">222</span> Development and Characterization of Biodegradable Films Based on Biopolymer Extracted From Natural Sources</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Dalila%20Hammiche">Dalila Hammiche</a>, <a href="https://publications.waset.org/abstracts/search?q=Lisa%20Klaai"> Lisa Klaai</a>, <a href="https://publications.waset.org/abstracts/search?q=Sonia%20Imzi"> Sonia Imzi</a>, <a href="https://publications.waset.org/abstracts/search?q=Amar%20Boukerrou"> Amar Boukerrou</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The fight against plastic pollution implies the development of polymers as alternatives to synthetic polymers. Starch is a natural polymer that can easily be plasticized by means of additives. The objective of this work is to develop and characterize biodegradable biofilms based on starch, plasticized by glycerol (20 and 30%). The elaboration of the biofilms was carried out by the casting method under simple conditions. The samples were characterized by infrared spectroscopy analysis with Fourier transform (FTIR), thermogravimetric analysis, and biodegradability test. Infrared spectral analysis showed that the 30% and 20% glycerol films have the same chemical structure and no functional group changes occurred. Thermogravimetric analysis showed that a 30% glycerol film has higher thermal stability than a 20% glycerol film. Biodegradability test showed that the lower the percentage of glycerol, the more easily the biofilm degrades. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=starch" title="starch">starch</a>, <a href="https://publications.waset.org/abstracts/search?q=natural%20sources" title=" natural sources"> natural sources</a>, <a href="https://publications.waset.org/abstracts/search?q=FTIR" title=" FTIR"> FTIR</a>, <a href="https://publications.waset.org/abstracts/search?q=thermogravimetric%20analysis" title=" thermogravimetric analysis"> thermogravimetric analysis</a>, <a href="https://publications.waset.org/abstracts/search?q=biodegradability%20test" title=" biodegradability test"> biodegradability test</a> </p> <a href="https://publications.waset.org/abstracts/149369/development-and-characterization-of-biodegradable-films-based-on-biopolymer-extracted-from-natural-sources" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/149369.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">102</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">221</span> Phase Transition in Iron Storage Protein Ferritin </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Navneet%20Kaur">Navneet Kaur</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20D.%20Tiwari"> S. D. Tiwari</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Ferritin is a protein which present in the blood of mammals. It maintains the need of iron inside the body. It has an antiferromagnetic iron core, 7-8 nm in size, which is encapsulated inside a protein cage. The thickness of this protein shell is about 2-3 nm. This protein shell reduces the interaction among particles and make ferritin a model superparamagnet. The major composition of ferritin core is mineral ferrihydrite. The molecular formula of ferritin core is (FeOOH)8[FeOOPO3H2]. In this study, we discuss the phase transition of ferritin. We characterized ferritin using x-ray diffractometer, transmission electron micrograph, thermogravimetric analyzer and vibrating sample magnetometer. It is found that ferritin core is amorphous in nature with average particle size of 8 nm. The thermogravimetric and differential thermogravimetric analysis curves shows mass loss at different temperatures. We heated ferritin at these temperatures. It is found that ferritin core starts decomposing after 390^o C. At 1020^o C, the ferritin core is finally converted to alpha phase of iron oxide. Magnetization behavior of final sample clearly shows the iron oxyhydroxide core is completely converted to alpha iron oxide. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Antiferromagnetic" title="Antiferromagnetic">Antiferromagnetic</a>, <a href="https://publications.waset.org/abstracts/search?q=Ferritin" title=" Ferritin"> Ferritin</a>, <a href="https://publications.waset.org/abstracts/search?q=Phase" title=" Phase"> Phase</a>, <a href="https://publications.waset.org/abstracts/search?q=Superparamagnetic" title=" Superparamagnetic"> Superparamagnetic</a> </p> <a href="https://publications.waset.org/abstracts/124547/phase-transition-in-iron-storage-protein-ferritin" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/124547.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">119</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">220</span> Analysis of CO₂ Capture Products from Carbon Capture and Utilization Plant</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Bongjae%20Lee">Bongjae Lee</a>, <a href="https://publications.waset.org/abstracts/search?q=Beom%20Goo%20Hwang"> Beom Goo Hwang</a>, <a href="https://publications.waset.org/abstracts/search?q=Hye%20Mi%20Park"> Hye Mi Park</a> </p> <p class="card-text"><strong>Abstract:</strong></p> CO₂ capture products manufactured through Carbon Capture and Utilization (CCU) Plant that collect CO₂ directly from power plants require accurate measurements of the amount of CO₂ captured. For this purpose, two tests were carried out on the weight loss test. And one was analyzed using a carbon dioxide quantification device. First, the ignition loss analysis was performed by measuring the weight of the sample at 550°C after the first conversation and then confirming the loss when ignited at 950°C. Second, in the thermogravimetric analysis, the sample was divided into two sections of 40 to 500°C and 500 to 800°C to confirm the reduction. The results of thermal weight loss analysis and thermogravimetric analysis were confirmed to be almost similar. However, the temperature of the ignition loss analysis method was 950°C, which was 150°C higher than that of the thermogravimetric method at a temperature of 800°C, so that the difference in the amount of weight loss was 3 to 4% higher by the heat loss analysis method. In addition, the tendency that the CO₂ content increases as the reaction time become longer is similarly confirmed. Third, the results of the wet titration method through the carbon dioxide quantification device were found to be significantly lower than the weight loss method. Therefore, based on the results obtained through the above three analysis methods, we will establish a method to analyze the accurate amount of CO₂. Acknowledgements: This work was supported by the Korea Institute of Energy Technology Evaluation and planning (No. 20152010201850). <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=carbon%20capture%20and%20utilization" title="carbon capture and utilization">carbon capture and utilization</a>, <a href="https://publications.waset.org/abstracts/search?q=CCU" title=" CCU"> CCU</a>, <a href="https://publications.waset.org/abstracts/search?q=CO2" title=" CO2"> CO2</a>, <a href="https://publications.waset.org/abstracts/search?q=CO2%20capture%20products" title=" CO2 capture products"> CO2 capture products</a>, <a href="https://publications.waset.org/abstracts/search?q=analysis%20method" title=" analysis method"> analysis method</a> </p> <a href="https://publications.waset.org/abstracts/75224/analysis-of-co2-capture-products-from-carbon-capture-and-utilization-plant" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/75224.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">218</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">219</span> Thermal Technologies Applications for Soil Remediation</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=A.%20de%20Folly%20d%E2%80%99Auris">A. de Folly d’Auris</a>, <a href="https://publications.waset.org/abstracts/search?q=R.%20Bagatin"> R. Bagatin</a>, <a href="https://publications.waset.org/abstracts/search?q=P.%20Filtri"> P. Filtri</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This paper discusses the importance of having a good initial characterization of soil samples when thermal desorption has to be applied to polluted soils for the removal of contaminants. Particular attention has to be devoted on the desorption kinetics of the samples to identify the gases evolved during the heating, and contaminant degradation pathways. In this study, two samples coming from different points of the same contaminated site were considered. The samples are much different from each other. Moreover, the presence of high initial quantity of heavy hydrocarbons strongly affected the performance of thermal desorption, resulting in formation of dangerous intermediates. Analytical techniques such TGA (Thermogravimetric Analysis), DSC (Differential Scanning Calorimetry) and GC-MS (Gas Chromatography-Mass) provided a good support to give correct indication for field application. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=desorption%20kinetics" title="desorption kinetics">desorption kinetics</a>, <a href="https://publications.waset.org/abstracts/search?q=hydrocarbons" title=" hydrocarbons"> hydrocarbons</a>, <a href="https://publications.waset.org/abstracts/search?q=thermal%20desorption" title=" thermal desorption"> thermal desorption</a>, <a href="https://publications.waset.org/abstracts/search?q=thermogravimetric%20measurements" title=" thermogravimetric measurements"> thermogravimetric measurements</a> </p> <a href="https://publications.waset.org/abstracts/40004/thermal-technologies-applications-for-soil-remediation" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/40004.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">295</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">218</span> Thermal Degradation Kinetics of Field-Dried and Pelletized Switchgrass</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Karen%20E.%20Supan">Karen E. Supan</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Thermal degradation kinetics of switchgrass (Panicum virgatum) from the field, as well as in a pellet form, are presented. Thermogravimetric analysis tests were performed at heating rates of 10-40 K min⁻¹ in an inert atmosphere. The activation energy and the pre-exponential factor were calculated using the Ozawa/Flynn/Wall method as suggested by the ASTM Standard Test Method for Decomposition Kinetics by Thermogravimetry. Four stages were seen in the degradation: dehydration, active pyrolysis of hemicellulose, active pyrolysis of cellulose, and passive pyrolysis. The derivative mass loss peak for active pyrolysis of cellulose in the field-dried sample was much higher than the pelletized. The range of activation energy in the 0.15 – 0.70 conversion interval was 191 – 242 kJ mol⁻¹ for the field-dried and 130-192 kJ mol⁻¹ for the pellets. The highest activation energies were achieved at 0.50 conversion and were 242 kJ mol⁻¹ and 192 kJ mol⁻¹ for the field-dried and pellets, respectively. The thermal degradation and activation energies were comparable to switchgrass and other biomass reported in the literature. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biomass" title="biomass">biomass</a>, <a href="https://publications.waset.org/abstracts/search?q=switchgrass" title=" switchgrass"> switchgrass</a>, <a href="https://publications.waset.org/abstracts/search?q=thermal%20degradation" title=" thermal degradation"> thermal degradation</a>, <a href="https://publications.waset.org/abstracts/search?q=thermogravimetric%20analysis" title=" thermogravimetric analysis"> thermogravimetric analysis</a> </p> <a href="https://publications.waset.org/abstracts/152009/thermal-degradation-kinetics-of-field-dried-and-pelletized-switchgrass" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/152009.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">116</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">217</span> Reaction Rate of Olive Stone during Combustion in a Bubbling Fluidized Bed</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=A.%20Soria-Verdugo">A. Soria-Verdugo</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Rubio-Rubio"> M. Rubio-Rubio</a>, <a href="https://publications.waset.org/abstracts/search?q=J.%20Arrieta"> J. Arrieta</a>, <a href="https://publications.waset.org/abstracts/search?q=N.%20Garc%C3%ADa-Hernando"> N. García-Hernando</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Combustion of biomass is a promising alternative to reduce the high pollutant emission levels associated to the combustion of fossil flues due to the net null emission of CO<sub>2</sub> attributed to biomass. However, the biomass selected should also have low contents of nitrogen and sulfur to limit the NO<sub>x</sub> and SO<sub>x</sub> emissions derived from its combustion. In this sense, olive stone is an excellent fuel to power combustion reactors with reduced levels of pollutant emissions. In this work, the combustion of olive stone particles is analyzed experimentally in a thermogravimetric analyzer (TGA) and in a bubbling fluidized bed reactor (BFB). The bubbling fluidized bed reactor was installed over a scale, conforming a macro-TGA. In both equipment, the evolution of the mass of the samples was registered as the combustion process progressed. The results show a much faster combustion process in the bubbling fluidized bed reactor compared to the thermogravimetric analyzer measurements, due to the higher heat transfer coefficient and the abrasion of the fuel particles by the bed material in the BFB reactor. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=olive%20stone" title="olive stone">olive stone</a>, <a href="https://publications.waset.org/abstracts/search?q=combustion" title=" combustion"> combustion</a>, <a href="https://publications.waset.org/abstracts/search?q=reaction%20rate" title=" reaction rate"> reaction rate</a>, <a href="https://publications.waset.org/abstracts/search?q=fluidized%20bed" title=" fluidized bed"> fluidized bed</a> </p> <a href="https://publications.waset.org/abstracts/89807/reaction-rate-of-olive-stone-during-combustion-in-a-bubbling-fluidized-bed" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/89807.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">201</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">216</span> Synthesis and Application of Tamarind Hydroxypropane Sulphonic Acid Resin for Removal of Heavy Metal Ions from Industrial Wastewater</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Aresh%20Vikram%20Singh">Aresh Vikram Singh</a>, <a href="https://publications.waset.org/abstracts/search?q=Sarika%20Nagar"> Sarika Nagar</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The tamarind based resin containing hydroxypropane sulphonic acid groups has been synthesized and their adsorption behavior for heavy metal ions has been investigated using batch and column experiments. The hydroxypropane sulphonic acid group has been incorporated onto tamarind by a modified Porath's method of functionalisation of polysaccharides. The tamarind hydroxypropane sulphonic acid (THPSA) resin can selectively remove of heavy metal ions, which are contained in industrial wastewater. The THPSA resin was characterized by FTIR and thermogravimetric analysis. The effects of various adsorption conditions, such as pH, treatment time and adsorbent dose were also investigated. The optimum adsorption condition was found at pH 6, 120 minutes of equilibrium time and 0.1 gram of resin dose. The orders of distribution coefficient values were determined. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=distribution%20coefficient" title="distribution coefficient">distribution coefficient</a>, <a href="https://publications.waset.org/abstracts/search?q=industrial%20wastewater" title=" industrial wastewater"> industrial wastewater</a>, <a href="https://publications.waset.org/abstracts/search?q=polysaccharides" title=" polysaccharides"> polysaccharides</a>, <a href="https://publications.waset.org/abstracts/search?q=tamarind%20hydroxypropane%20sulphonic%20acid%20resin" title=" tamarind hydroxypropane sulphonic acid resin"> tamarind hydroxypropane sulphonic acid resin</a>, <a href="https://publications.waset.org/abstracts/search?q=thermogravimetric%20analysis" title=" thermogravimetric analysis"> thermogravimetric analysis</a>, <a href="https://publications.waset.org/abstracts/search?q=THPSA" title=" THPSA"> THPSA</a> </p> <a href="https://publications.waset.org/abstracts/64604/synthesis-and-application-of-tamarind-hydroxypropane-sulphonic-acid-resin-for-removal-of-heavy-metal-ions-from-industrial-wastewater" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/64604.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">261</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">215</span> Mechanical Behavior of Recycled Mortars Manufactured from Moisture Correction Using the Halogen Light Thermogravimetric Balance as an Alternative to the Traditional ASTM C 128 Method</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Diana%20Gomez-Cano">Diana Gomez-Cano</a>, <a href="https://publications.waset.org/abstracts/search?q=J.%20C.%20Ochoa-Botero"> J. C. Ochoa-Botero</a>, <a href="https://publications.waset.org/abstracts/search?q=Roberto%20Bernal%20Correa"> Roberto Bernal Correa</a>, <a href="https://publications.waset.org/abstracts/search?q=Yhan%20Paul%20Arias"> Yhan Paul Arias</a> </p> <p class="card-text"><strong>Abstract:</strong></p> To obtain high mechanical performance, the fresh conditions of a mortar are decisive. Measuring the absorption of aggregates used in mortar mixes is a fundamental requirement for proper design of the mixes prior to their placement in construction sites. In this sense, absorption is a determining factor in the design of a mix because it conditions the amount of water, which in turn affects the water/cement ratio and the final porosity of the mortar. Thus, this work focuses on the mechanical behavior of recycled mortars manufactured from moisture correction using the Thermogravimetric Balancing Halogen Light (TBHL) technique in comparison with the traditional ASTM C 128 International Standard method. The advantages of using the TBHL technique are favorable in terms of reduced consumption of resources such as materials, energy, and time. The results show that in contrast to the ASTM C 128 method, the TBHL alternative technique allows obtaining a higher precision in the absorption values of recycled aggregates, which is reflected not only in a more efficient process in terms of sustainability in the characterization of construction materials but also in an effect on the mechanical performance of recycled mortars. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=alternative%20raw%20materials" title="alternative raw materials">alternative raw materials</a>, <a href="https://publications.waset.org/abstracts/search?q=halogen%20light" title=" halogen light"> halogen light</a>, <a href="https://publications.waset.org/abstracts/search?q=recycled%20mortar" title=" recycled mortar"> recycled mortar</a>, <a href="https://publications.waset.org/abstracts/search?q=resources%20optimization" title=" resources optimization"> resources optimization</a>, <a href="https://publications.waset.org/abstracts/search?q=water%20absorption" title=" water absorption"> water absorption</a> </p> <a href="https://publications.waset.org/abstracts/134430/mechanical-behavior-of-recycled-mortars-manufactured-from-moisture-correction-using-the-halogen-light-thermogravimetric-balance-as-an-alternative-to-the-traditional-astm-c-128-method" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/134430.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">114</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">214</span> Ultrasound-Assisted Extraction of Bioactive Compounds from Cocoa Shell and Their Encapsulation in Gum Arabic and Maltodextrin: A Technology to Produce Functional Food Ingredients</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Saeid%20Jafari">Saeid Jafari</a>, <a href="https://publications.waset.org/abstracts/search?q=Khursheed%20Ahmad%20Sheikh"> Khursheed Ahmad Sheikh</a>, <a href="https://publications.waset.org/abstracts/search?q=Randy%20W.%20Worobo"> Randy W. Worobo</a>, <a href="https://publications.waset.org/abstracts/search?q=Kitipong%20Assatarakul"> Kitipong Assatarakul</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this study, the extraction of cocoa shell powder (CSP) was optimized, and the optimized extracts were spray-dried for encapsulation purposes. Temperature (45-65 ◦C), extraction time (30–60 min), and ethanol concentration (60–100%) were the extraction parameters. The response surface methodology analysis revealed that the model was significant (p ≤ 0.05) in interactions between all variables (total phenolic compound, total flavonoid content, and antioxidant activity as measured by 2,2-Diphenyl-1-picrylhydrazyl (DPPH) and ferric reducing antioxidant power (FRAP assays), with a lack of fit test for the model being insignificant (p > 0.05). Temperature (55 ◦C), time (45 min), and ethanol concentration (60%) were found to be the optimal extraction conditions. For spray-drying encapsulation, some quality metrics (e.g., water solubility, water activity) were insignificant (p > 0.05). The microcapsules were found to be spherical in shape using a scanning electron microscope. Thermogravimetric and differential thermogravimetric measurements of the microcapsules revealed nearly identical results. The gum arabic + maltodextrin microcapsule (GMM) showed potential antibacterial (zone of inhibition: 11.50 mm; lower minimum inhibitory concentration: 1.50 mg/mL) and antioxidant (DPPH: 1063 mM trolox/100g dry wt.) activities (p ≤ 0.05). In conclusion, the microcapsules in this study, particularly GMM, are promising antioxidant and antibacterial agents to be fortified as functional food ingredients for the production of nutraceutical foods with health-promoting properties. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=functional%20foods" title="functional foods">functional foods</a>, <a href="https://publications.waset.org/abstracts/search?q=coco%20shell%20powder" title=" coco shell powder"> coco shell powder</a>, <a href="https://publications.waset.org/abstracts/search?q=antioxidant%20activity" title=" antioxidant activity"> antioxidant activity</a>, <a href="https://publications.waset.org/abstracts/search?q=encapsulation" title=" encapsulation"> encapsulation</a>, <a href="https://publications.waset.org/abstracts/search?q=extraction" title=" extraction"> extraction</a> </p> <a href="https://publications.waset.org/abstracts/181855/ultrasound-assisted-extraction-of-bioactive-compounds-from-cocoa-shell-and-their-encapsulation-in-gum-arabic-and-maltodextrin-a-technology-to-produce-functional-food-ingredients" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/181855.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">57</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">213</span> Preparation of Chemically Activated Carbon from Waste Tire Char for Lead Ions Adsorption and Optimization Using Response Surface Methodology</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Lucky%20Malise">Lucky Malise</a>, <a href="https://publications.waset.org/abstracts/search?q=Hilary%20Rutto"> Hilary Rutto</a>, <a href="https://publications.waset.org/abstracts/search?q=Tumisang%20Seodigeng"> Tumisang Seodigeng</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The use of tires in automobiles is very important in the automobile industry. However, there is a serious environmental problem concerning the disposal of these rubber tires once they become worn out. The main aim of this study was to prepare activated carbon from waste tire pyrolysis char by impregnating KOH on pyrolytic char. Adsorption studies on lead onto chemically activated carbon was carried out using response surface methodology. The effect of process parameters such as temperature (°C), adsorbent dosage (g/1000ml), pH, contact time (minutes) and initial lead concentration (mg/l) on the adsorption capacity were investigated. It was found that the adsorption capacity increases with an increase in contact time, pH, temperature and decreases with an increase in lead concentration. Optimization of the process variables was done using a numerical optimization method. Fourier Transform Infrared Spectra (FTIR) analysis, XRay diffraction (XRD), Thermogravimetric analysis (TGA) and scanning electron microscope was used to characterize the pyrolytic carbon char before and after activation. The optimum points 1g/ 100 ml for adsorbent dosage, 7 for pH value of the solution, 115.2 min for contact time, 100 mg/l for initial metal concentration, and 25°C for temperature were obtained to achieve the highest adsorption capacity of 93.176 mg/g with a desirability of 0.994. Fourier Transform Infrared Spectra (FTIR) analysis and Thermogravimetric analysis (TGA) show the presence of oxygen-containing functional groups on the surface of the activated carbon produced and that the weight loss taking place during the activation step is small. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=waste%20tire%20pyrolysis%20char" title="waste tire pyrolysis char">waste tire pyrolysis char</a>, <a href="https://publications.waset.org/abstracts/search?q=chemical%20activation" title=" chemical activation"> chemical activation</a>, <a href="https://publications.waset.org/abstracts/search?q=central%20composite%20design%20%28CCD%29" title=" central composite design (CCD)"> central composite design (CCD)</a>, <a href="https://publications.waset.org/abstracts/search?q=adsorption%20capacity" title=" adsorption capacity"> adsorption capacity</a>, <a href="https://publications.waset.org/abstracts/search?q=numerical%20optimization" title=" numerical optimization"> numerical optimization</a> </p> <a href="https://publications.waset.org/abstracts/78877/preparation-of-chemically-activated-carbon-from-waste-tire-char-for-lead-ions-adsorption-and-optimization-using-response-surface-methodology" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/78877.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">226</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">212</span> Development of a Cathode-Type Ca1-xSrxMnO3</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=A.%20Guemache">A. Guemache</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Omari"> M. Omari </a> </p> <p class="card-text"><strong>Abstract:</strong></p> Oxides with formula Ca1-xSrx MnO3 (0≤x≤0.2) were synthesized using co-precipitation method. The identification of the obtained phase was carried out using infrared spectroscopy and X-ray diffraction. Thermogravimetric and differential analysis was permitted to characterize different transformations of precursors which take place during one heating cycle. The study of electrochemical behavior was carried out by cyclic voltammetry and impedance spectroscopy. The obtained results show that apparent catalytic activity improved when increasing the concentration of strontium. Anodic current densities varies from 1.3 to 5.9 mA/cm2 at the rate scan of 20 mV.s-1 and a potential 0.8 V for oxides with composition x=0 to 0.2. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=oxide" title="oxide">oxide</a>, <a href="https://publications.waset.org/abstracts/search?q=co-precipitation" title=" co-precipitation"> co-precipitation</a>, <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20properties" title=" electrochemical properties"> electrochemical properties</a>, <a href="https://publications.waset.org/abstracts/search?q=cathode-type" title=" cathode-type"> cathode-type</a> </p> <a href="https://publications.waset.org/abstracts/14852/development-of-a-cathode-type-ca1-xsrxmno3" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/14852.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">291</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">211</span> Synthesis and Characterization of a Type Oxide Ca1-x Srx MnO3</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=A.%20Guemache">A. Guemache</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Omari"> M. Omari</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Oxides with formula Ca1-xSrx MnO3(0≤x≤0.2) were synthesized using co precipitation method. The identification of the obtained phase was carried out using infrared spectroscopy and x-ray diffraction. Thermogravimetric and differential analysis was permitted to characterize different transformations of precursors which take place during one heating cycle. The study of electrochemical behavior was carried out by cyclic voltammetry and impedance spectroscopy. The obtained results show that apparent catalytic activity improved when increasing the concentration of strontium. Anodic current densities varies from 1.3 to 5.9 mA/cm2 at the rate scan of 20 mV.s-1 and a potential 0.8 V for oxides with composition x=0 to 0.2. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=oxide" title="oxide">oxide</a>, <a href="https://publications.waset.org/abstracts/search?q=co-precipitation" title=" co-precipitation"> co-precipitation</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=electrochemical%20properties" title=" electrochemical properties"> electrochemical properties</a> </p> <a href="https://publications.waset.org/abstracts/14851/synthesis-and-characterization-of-a-type-oxide-ca1-x-srx-mno3" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/14851.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">362</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">210</span> Synthesis of High-Pressure Performance Adsorbent from Coconut Shells Polyetheretherketone for Methane Adsorption</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Umar%20Hayatu%20Sidik">Umar Hayatu Sidik</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Application of liquid base petroleum fuel (petrol and diesel) for transportation fuel causes emissions of greenhouse gases (GHGs), while natural gas (NG) reduces the emissions of greenhouse gases (GHGs). At present, compression and liquefaction are the most matured technology used for transportation system. For transportation use, compression requires high pressure (200–300 bar) while liquefaction is impractical. A relatively low pressure of 30-40 bar is achievable by adsorbed natural gas (ANG) to store nearly compressed natural gas (CNG). In this study, adsorbents for high-pressure adsorption of methane (CH4) was prepared from coconut shells and polyetheretherketone (PEEK) using potassium hydroxide (KOH) and microwave-assisted activation. Design expert software version 7.1.6 was used for optimization and prediction of preparation conditions of the adsorbents for CH₄ adsorption. Effects of microwave power, activation time and quantity of PEEK on the adsorbents performance toward CH₄ adsorption was investigated. The adsorbents were characterized by Fourier transform infrared spectroscopy (FTIR), thermogravimetric (TG) and derivative thermogravimetric (DTG) and scanning electron microscopy (SEM). The ideal CH4 adsorption capacities of adsorbents were determined using volumetric method at pressures of 5, 17, and 35 bar at an ambient temperature and 5 oC respectively. Isotherm and kinetics models were used to validate the experimental results. The optimum preparation conditions were found to be 15 wt% amount of PEEK, 3 minutes activation time and 300 W microwave power. The highest CH4 uptake of 9.7045 mmol CH4 adsorbed/g adsorbent was recorded by M33P15 (300 W of microwave power, 3 min activation time and 15 wt% amount of PEEK) among the sorbents at an ambient temperature and 35 bar. The CH4 equilibrium data is well correlated with Sips, Toth, Freundlich and Langmuir. Isotherms revealed that the Sips isotherm has the best fit, while the kinetics studies revealed that the pseudo-second-order kinetic model best describes the adsorption process. In all scenarios studied, a decrease in temperature led to an increase in adsorption of both gases. The adsorbent (M33P15) maintained its stability even after seven adsorption/desorption cycles. The findings revealed the potential of coconut shell-PEEK as CH₄ adsorbents. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=adsorption" title="adsorption">adsorption</a>, <a href="https://publications.waset.org/abstracts/search?q=desorption" title=" desorption"> desorption</a>, <a href="https://publications.waset.org/abstracts/search?q=activated%20carbon" title=" activated carbon"> activated carbon</a>, <a href="https://publications.waset.org/abstracts/search?q=coconut%20shells" title=" coconut shells"> coconut shells</a>, <a href="https://publications.waset.org/abstracts/search?q=polyetheretherketone" title=" polyetheretherketone"> polyetheretherketone</a> </p> <a href="https://publications.waset.org/abstracts/176392/synthesis-of-high-pressure-performance-adsorbent-from-coconut-shells-polyetheretherketone-for-methane-adsorption" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/176392.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">67</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">209</span> Detailed Investigation of Thermal Degradation Mechanism and Product Characterization of Co-Pyrolysis of Indian Oil Shale with Rubber Seed Shell</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Bhargav%20Baruah">Bhargav Baruah</a>, <a href="https://publications.waset.org/abstracts/search?q=Ali%20Shemsedin%20Reshad"> Ali Shemsedin Reshad</a>, <a href="https://publications.waset.org/abstracts/search?q=Pankaj%20Tiwari"> Pankaj Tiwari</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This work presents a detailed study on the thermal degradation kinetics of co-pyrolysis of oil shale of Upper Assam, India with rubber seed shell, and lab-scale pyrolysis to investigate the influence of pyrolysis parameters on product yield and composition of products. The physicochemical characteristics of oil shale and rubber seed shell were studied by proximate analysis, elemental analysis, Fourier transform infrared spectroscopy and X-ray diffraction. The physicochemical study showed the mixture to be of low moisture, high ash, siliceous, sour with the presence of aliphatic, aromatic, and phenolic compounds. The thermal decomposition of the oil shale with rubber seed shell was studied using thermogravimetric analysis at heating rates of 5, 10, 20, 30, and 50 °C/min. The kinetic study of the oil shale pyrolysis process was performed on the thermogravimetric (TGA) data using three model-free isoconversional methods viz. Friedman, Flynn Wall Ozawa (FWO), and Kissinger Akahira Sunnose (KAS). The reaction mechanisms were determined using the Criado master plot. The understanding of the composition of Indian oil shale and rubber seed shell and pyrolysis process kinetics can help to establish the experimental parameters for the extraction of valuable products from the mixture. Response surface methodology (RSM) was employed usinf central composite design (CCD) model to setup the lab-scale experiment using TGA data, and optimization of process parameters viz. heating rate, temperature, and particle size. The samples were pre-dried at 115°C for 24 hours prior to pyrolysis. The pyrolysis temperatures were set from 450 to 650 °C, at heating rates of 2 to 20°C/min. The retention time was set between 2 to 8 hours. The optimum oil yield was observed at 5°C/min and 550°C with a retention time of 5 hours. The pyrolytic oil and gas obtained at optimum conditions were subjected to characterization using Fourier transform infrared spectroscopy (FT-IR) gas chromatography and mass spectrometry (GC-MS) and nuclear magnetic resonance spectroscopy (NMR). <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Indian%20oil%20shale" title="Indian oil shale">Indian oil shale</a>, <a href="https://publications.waset.org/abstracts/search?q=rubber%20seed%20shell" title=" rubber seed shell"> rubber seed shell</a>, <a href="https://publications.waset.org/abstracts/search?q=co-pyrolysis" title=" co-pyrolysis"> co-pyrolysis</a>, <a href="https://publications.waset.org/abstracts/search?q=isoconversional%20methods" title=" isoconversional methods"> isoconversional methods</a>, <a href="https://publications.waset.org/abstracts/search?q=gas%20chromatography" title=" gas chromatography"> gas chromatography</a>, <a href="https://publications.waset.org/abstracts/search?q=nuclear%20magnetic%20resonance" title=" nuclear magnetic resonance"> nuclear magnetic resonance</a>, <a href="https://publications.waset.org/abstracts/search?q=Fourier%20transform%20infrared%20spectroscopy" title=" Fourier transform infrared spectroscopy"> Fourier transform infrared spectroscopy</a> </p> <a href="https://publications.waset.org/abstracts/117026/detailed-investigation-of-thermal-degradation-mechanism-and-product-characterization-of-co-pyrolysis-of-indian-oil-shale-with-rubber-seed-shell" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/117026.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">146</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">208</span> Utilization of Low-Cost Adsorbent Fly Ash for the Removal of Phenol from Water</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ihsanullah">Ihsanullah</a>, <a href="https://publications.waset.org/abstracts/search?q=Muataz%20Ali%20Atieh"> Muataz Ali Atieh</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this study, a low-cost adsorbent carbon fly ash (CFA) was used for the removal of Phenol from the water. The adsorbent characteristics were observed by the Thermogravimetric Analysis (TGA), BET specific surface area analyzer, Zeta Potential and Field Emission Scanning Electron Microscopy (FE-SEM). The effect of pH, agitation speed, contact time, adsorbent dosage, and initial concentration of phenol were studied on the removal of phenol from the water. The optimum values of these variables for maximum removal of phenol were also determined. Both Freundlich and Langmuir isotherm models were successfully applied to describe the experimental data. Results showed that low-cost adsorbent phenol can be successfully applied for the removal of Phenol from the water. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=phenol" title="phenol">phenol</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=adsorption" title=" adsorption"> adsorption</a>, <a href="https://publications.waset.org/abstracts/search?q=carbon%20adsorbents" title=" carbon adsorbents"> carbon adsorbents</a> </p> <a href="https://publications.waset.org/abstracts/19609/utilization-of-low-cost-adsorbent-fly-ash-for-the-removal-of-phenol-from-water" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/19609.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">325</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">207</span> Synthesis of Nanoparticle Mordenite Zeolite for Dimethyl Ether Carbonylation</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Zhang%20Haitao">Zhang Haitao</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The different size of nanoparticle mordenite zeolites were prepared by adding different soft template during hydrothermal process for carbonylation of dimethyl ether (DME) to methyl acetate (MA). The catalysts were characterized by X-ray diffraction, Ar adsorption-desorption, high-resolution transmission electron microscopy, NH3-temperature programmed desorption, scanning electron microscopy and Thermogravimetric. The characterization results confirmed that mordenite zeolites with small nanoparticle showed more strong acid sites which was the active site for carbonylation thus promoting conversion of DME and MA selectivity. Furthermore, the nanoparticle mordenite had increased the mass transfer efficiency which could suppress the formation of coke. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=nanoparticle%20mordenite" title="nanoparticle mordenite">nanoparticle mordenite</a>, <a href="https://publications.waset.org/abstracts/search?q=carbonylation" title=" carbonylation"> carbonylation</a>, <a href="https://publications.waset.org/abstracts/search?q=dimethyl%20ether" title=" dimethyl ether"> dimethyl ether</a>, <a href="https://publications.waset.org/abstracts/search?q=methyl%20acetate" title=" methyl acetate"> methyl acetate</a> </p> <a href="https://publications.waset.org/abstracts/120694/synthesis-of-nanoparticle-mordenite-zeolite-for-dimethyl-ether-carbonylation" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/120694.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">140</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">206</span> Design and Synthesis of Gradient Nanocomposite Materials</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Pu%20Ying-Chih">Pu Ying-Chih</a>, <a href="https://publications.waset.org/abstracts/search?q=Yang%20Yin-Ju"> Yang Yin-Ju</a>, <a href="https://publications.waset.org/abstracts/search?q=Hang%20Jian-Yi"> Hang Jian-Yi</a>, <a href="https://publications.waset.org/abstracts/search?q=Jang%20Guang-Way"> Jang Guang-Way </a> </p> <p class="card-text"><strong>Abstract:</strong></p> Organic-Inorganic hybrid materials consisting of graded distributions of inorganic nano particles in organic polymer matrices were successfully prepared by the sol-gel process. Optical and surface properties of the resulting nano composites can be manipulated by changing their compositions and nano particle distribution gradients. Applications of gradient nano composite materials include sealants for LED packaging and screen lenses for smartphones. Optical transparency, prism coupler, TEM, SEM, Energy Dispersive X-ray Spectrometer (EDX), Izod impact strength, conductivity, pencil hardness, and thermogravimetric characterizations of the nano composites were performed and the results will be presented. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Gradient" title="Gradient">Gradient</a>, <a href="https://publications.waset.org/abstracts/search?q=Hybrid" title=" Hybrid"> Hybrid</a>, <a href="https://publications.waset.org/abstracts/search?q=Nanocomposite" title=" Nanocomposite"> Nanocomposite</a>, <a href="https://publications.waset.org/abstracts/search?q=Organic-Inorganic" title=" Organic-Inorganic"> Organic-Inorganic</a> </p> <a href="https://publications.waset.org/abstracts/25011/design-and-synthesis-of-gradient-nanocomposite-materials" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/25011.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">506</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">205</span> Study on the Controlled Growth of Lanthanum Hydroxide and Manganese Oxide Nano Composite under the Presence of Cationic Surfactant</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Neeraj%20Kumar%20Verma">Neeraj Kumar Verma</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Lanthanum hydroxide and manganese oxide nanocomposite are synthesized by chemical routes. Physical characterization is done by TEM to look at the size and dispersion of the nanoparticles in the composite. Chemical characterization is done by X-ray diffraction technique and FTIR to ascertain the attachment of the functionalities and bond stretching. Further thermal analysis is done by thermogravimetric analysis to find the tendency of the thermal decomposition in the elevated temperature range of 0-1000°C. Proper analysis and correlation of the various results obtained suggested the controlled growth of crystalline without agglomeration and good stability in the various temperature ranges of the composite. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=nanoparticles" title="nanoparticles">nanoparticles</a>, <a href="https://publications.waset.org/abstracts/search?q=XRD" title=" XRD"> XRD</a>, <a href="https://publications.waset.org/abstracts/search?q=TEM" title=" TEM"> TEM</a>, <a href="https://publications.waset.org/abstracts/search?q=lanthanum%20hydroxide" title=" lanthanum hydroxide"> lanthanum hydroxide</a>, <a href="https://publications.waset.org/abstracts/search?q=manganese%20oxide" title=" manganese oxide"> manganese oxide</a> </p> <a href="https://publications.waset.org/abstracts/25803/study-on-the-controlled-growth-of-lanthanum-hydroxide-and-manganese-oxide-nano-composite-under-the-presence-of-cationic-surfactant" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/25803.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">471</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">204</span> Preparation of Nanocrystalline Mesoporous ThO2 Via Surfactant Assisted Sol-gel Procedure </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=N.%20Mohseni">N. Mohseni</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20Janitabar"> S. Janitabar</a>, <a href="https://publications.waset.org/abstracts/search?q=S.J.%20Ahmadi"> S.J. Ahmadi</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Roshanzamir"> M. Roshanzamir</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Thaghizadeh"> M. Thaghizadeh</a> </p> <p class="card-text"><strong>Abstract:</strong></p> There has been proposed a technique for getting thorium dioxide mesoporous nanocrystalline. In this paper thorium dioxide powder was synthesized through the sol-gel method using hydrated thorium nitrate and ammonium hydroxide as starting materials and Triton X100 as surfactant. ThO2 gel was characterized by thermogravimetric (TG), and prepared ThO2 powder was subjected to scanning electron microscopy (SEM), X-ray diffraction (XRD), and Brunauer-Emett-Teller (BET) analyses studies. Detailed analyses show that prepared powder consisted of phase with the space group Fm3m of thoria and its crystalline size was 27 nm. The thoria possesses 16.7 m2/g surface area and the pore volume and size calculated to be 0.0423 cc/g and 1.947 nm, respectively. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=mesoporous" title="mesoporous">mesoporous</a>, <a href="https://publications.waset.org/abstracts/search?q=nanocrystalline" title=" nanocrystalline"> nanocrystalline</a>, <a href="https://publications.waset.org/abstracts/search?q=sol-gel" title="sol-gel">sol-gel</a>, <a href="https://publications.waset.org/abstracts/search?q=thoria" title=" thoria "> thoria </a> </p> <a href="https://publications.waset.org/abstracts/24862/preparation-of-nanocrystalline-mesoporous-tho2-via-surfactant-assisted-sol-gel-procedure" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/24862.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">203</span> CO2 Capture in Porous Silica Assisted by Lithium</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Lucero%20Gonzalez">Lucero Gonzalez</a>, <a href="https://publications.waset.org/abstracts/search?q=Salvador%20Alfaro"> Salvador Alfaro</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Carbon dioxide (CO2) and methane (CH4) are considered as the compounds with higher abundance among the greenhouse gases (CO2, NOx, SOx, CxHx, etc.), due to its higher concentration, this two gases have a greater impact in the environment pollution and provokes global warming. So, recovery, disposal and subsequent reuse, are of great interest, especially from the ecological and health perspective. By one hand, porous inorganic materials are good candidates to capture gases, because these type of materials are higher stability from the point view of thermal, chemical and mechanical under adsorption gas processes. By another hand, during the design and the synthetic preparation of the porous materials is possible add other intrinsic properties (physicochemical and structural) by adding chemical compounds as dopants or using structured directed agents or surfactants to improve the porous structure, the above features allow to have alternative materials for separation, capture and storage of greenhouse gases. In this work, ordered mesoporous materials base silica were prepared using Surfynol as surfactant. The surfactant micelles are commonly used as self-assembly templates for the development of new structure porous silica’s, adding a variety of textures and structures. By another hand, the Surfynol is a commercial surfactant, is non-ionic, for that is necessary determine its critical micelles concentration (cmc) by the pyrene I1/I3 ratio method, before to prepare silica particles. One time known the CMC, a precursor gel was prepared via sol-gel process at room temperature using TEOS as silica precursor, NH4OH as catalyst, Surfynol as template and H2O as solvent. Then, the gel precursor was treatment hydrothermally in a Teflon-lined stainless steel autoclave with a volume of 100 mL and kept at 100 ºC for 24 h under static conditions in a convection oven. After that, the porous silica particles obtained were impregnated with lithium to improve the CO2 adsorption capacity. Then the silica particles were characterized physicochemical, morphology and structurally, by XRD, FTIR, BET and SEM techniques. The thermal stability and the CO2 adsorption capacity was evaluated by thermogravimetric analysis (TGA). According the results, we found that the Surfynol is a good candidate to prepare silica particles with an ordered structure. Also the TGA analysis shown that the particles has a good thermal stability in the range of 250 °C and 800 °C. The best materials had, the capacity to adsorbing 70 and 90 mg per gram of silica particles and its CO2 adsorption capacity depends on the way to thermal pretreatment of the porous silica before of the adsorption experiments and of the concentration of surfactant used during the synthesis of silica particles. Acknowledgments: This work was supported by SIP-IPN through project SIP-20161862. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=CO2%20adsorption" title="CO2 adsorption">CO2 adsorption</a>, <a href="https://publications.waset.org/abstracts/search?q=lithium%20as%20dopant" title=" lithium as dopant"> lithium as dopant</a>, <a href="https://publications.waset.org/abstracts/search?q=porous%20silica" title=" porous silica"> porous silica</a>, <a href="https://publications.waset.org/abstracts/search?q=surfynol%20as%20surfactant" title=" surfynol as surfactant"> surfynol as surfactant</a>, <a href="https://publications.waset.org/abstracts/search?q=thermogravimetric%20analysis" title=" thermogravimetric analysis"> thermogravimetric analysis</a> </p> <a href="https://publications.waset.org/abstracts/58168/co2-capture-in-porous-silica-assisted-by-lithium" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/58168.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">268</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">202</span> Properties of Poly(Amide-Imide) with Low Residual Stress for Electronic Material</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Kwangin%20Kim">Kwangin Kim</a>, <a href="https://publications.waset.org/abstracts/search?q=Taewon%20Yoo"> Taewon Yoo</a>, <a href="https://publications.waset.org/abstracts/search?q=Haksoo%20Han"> Haksoo Han</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Polyimide is a superior polymer in the electronics industry, and we conducted a study to synthesize poly(amide-imide) at low temperatures. Poly(amide-imide) was synthesized at low-temperature curing to offer a thermal stable membrane with low residual stress and good processability. As a result, the low crack polymer with good processability could be used to various applications such as semiconductors, integrated circuits, coating materials, membranes, and display. The synthesis of poly(amide-imide) at low temperatures was confirmed by Fourier transform infrared spectroscopy (FT-IR). Thermal stabilities of the polymer was confirmed by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=poly%28amide-imide%29" title="poly(amide-imide)">poly(amide-imide)</a>, <a href="https://publications.waset.org/abstracts/search?q=residual%20stress" title=" residual stress"> residual stress</a>, <a href="https://publications.waset.org/abstracts/search?q=thermal%20stability" title=" thermal stability"> thermal stability</a> </p> <a href="https://publications.waset.org/abstracts/23349/properties-of-polyamide-imide-with-low-residual-stress-for-electronic-material" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/23349.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">419</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">201</span> Effect of Aryl Imidazolium Ionic Liquids as Asphaltene Dispersants</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Raghda%20Ahmed%20El-Nagar">Raghda Ahmed El-Nagar</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Oil spills are one of the most serious environmental issues that have occurred during the production and transportation of petroleum crude oil. Chemical asphaltene dispersants are hazardous to the marine environment, so Ionic liquids (ILs) as asphaltene dispersants are a critical area of study. In this work, different aryl imidazolium ionic liquids were synthesized with high yield and elucidated via tools of analysis (Elemental analysis, FT-IR, and 1H-NMR). Thermogravimetric analysis confirmed that the prepared ILs posses high thermal stability. The critical micelle concentration (CMC), surface tension, and emulsification index were investigated. Evaluation of synthesized ILs as asphaltene dispersants were assessed at various concentrations, and data reveals high dispersion efficiency. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=ionic%20liquids" title="ionic liquids">ionic liquids</a>, <a href="https://publications.waset.org/abstracts/search?q=oil%20spill" title=" oil spill"> oil spill</a>, <a href="https://publications.waset.org/abstracts/search?q=asphaltene%20dispersants" title=" asphaltene dispersants"> asphaltene dispersants</a>, <a href="https://publications.waset.org/abstracts/search?q=CMC" title=" CMC"> CMC</a>, <a href="https://publications.waset.org/abstracts/search?q=efficiency" title=" efficiency"> efficiency</a> </p> <a href="https://publications.waset.org/abstracts/141084/effect-of-aryl-imidazolium-ionic-liquids-as-asphaltene-dispersants" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/141084.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">194</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">200</span> Self-Assembling Layered Double Hydroxide Nanosheets on β-FeOOH Nanorods for Reducing Fire Hazards of Epoxy Resin</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Wei%20Wang">Wei Wang</a>, <a href="https://publications.waset.org/abstracts/search?q=Yuan%20Hu"> Yuan Hu</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Epoxy resins (EP), one of the most important thermosetting polymers, is widely applied in various fields due to its desirable properties, such as excellent electrical insulation, low shrinkage, outstanding mechanical stiffness, satisfactory adhesion and solvent resistance. However, like most of the polymeric materials, EP has the fatal drawbacks including inherent flammability and high yield of toxic smoke, which restricts its application in the fields requiring fire safety. So, it is still a challenge and an interesting subject to develop new flame retardants which can not only remarkably improve the flame retardancy, but also render modified resins low toxic gases generation. In recent work, polymer nanocomposites based on nanohybrids that contain two or more kinds of nanofillers have drawn intensive interest, which can realize performance enhancements. The realization of previous hybrids of carbon nanotubes (CNTs) and molybdenum disulfide provides us a novel route to decorate layered double hydroxide (LDH) nanosheets on the surface of β-FeOOH nanorods; the deposited LDH nanosheets can fill the network and promote the work efficiency of β-FeOOH nanorods. Moreover, the synergistic effects between LDH and β-FeOOH can be anticipated to have potential applications in reducing fire hazards of EP composites for the combination of condense-phase and gas-phase mechanism. As reported, β-FeOOH nanorods can act as a core to prepare hybrid nanostructures combining with other nanoparticles through electrostatic attraction through layer-by-layer assembly technique. In this work, LDH nanosheets wrapped β-FeOOH nanorods (LDH-β-FeOOH) hybrids was synthesized by a facile method, with the purpose of combining the characteristics of one dimension (1D) and two dimension (2D), to improve the fire resistance of epoxy resin. The hybrids showed a well dispersion in EP matrix and had no obvious aggregation. Thermogravimetric analysis and cone calorimeter tests confirmed that LDH-β-FeOOH hybrids into EP matrix with a loading of 3% could obviously improve the fire safety of EP composites. The plausible flame retardancy mechanism was explored by thermogravimetric infrared (TG-IR) and X-ray photoelectron spectroscopy. The reasons were concluded: condense-phase and gas-phase. Nanofillers were transferred to the surface of matrix during combustion, which could not only shield EP matrix from external radiation and heat feedback from the fire zone, but also efficiently retard transport of oxygen and flammable pyrolysis. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=fire%20hazards" title="fire hazards">fire hazards</a>, <a href="https://publications.waset.org/abstracts/search?q=toxic%20gases" title=" toxic gases"> toxic gases</a>, <a href="https://publications.waset.org/abstracts/search?q=self-assembly" title=" self-assembly"> self-assembly</a>, <a href="https://publications.waset.org/abstracts/search?q=epoxy" title=" epoxy"> epoxy</a> </p> <a href="https://publications.waset.org/abstracts/80450/self-assembling-layered-double-hydroxide-nanosheets-on-v-feooh-nanorods-for-reducing-fire-hazards-of-epoxy-resin" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/80450.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">174</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">199</span> Gas-Solid Nitrocarburizing of Steels: Kinetic Modelling and Experimental Validation</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=L.%20Torchane">L. Torchane</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This study is devoted to defining the optimal conditions for the nitriding of pure iron at atmospheric pressure by using NH3-Ar-C3H8 gas mixtures. After studying the mechanisms of phase formation and mass transfer at the gas-solid interface, a mathematical model is developed in order to predict the nitrogen transfer rate in the solid, the ε-carbonitride layer growth rate and the nitrogen and carbon concentration profiles. In order to validate the model and to show its possibilities, it is compared with thermogravimetric experiments, analyses and metallurgical observations (X-ray diffraction, optical microscopy and electron microprobe analysis). Results obtained allow us to demonstrate the sound correlation between the experimental results and the theoretical predictions. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=gaseous%20nitrocarburizing" title="gaseous nitrocarburizing">gaseous nitrocarburizing</a>, <a href="https://publications.waset.org/abstracts/search?q=kinetic%20model" title=" kinetic model"> kinetic model</a>, <a href="https://publications.waset.org/abstracts/search?q=diffusion" title=" diffusion"> diffusion</a>, <a href="https://publications.waset.org/abstracts/search?q=layer%20growth%20kinetic" title=" layer growth kinetic"> layer growth kinetic</a> </p> <a href="https://publications.waset.org/abstracts/15796/gas-solid-nitrocarburizing-of-steels-kinetic-modelling-and-experimental-validation" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/15796.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">534</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">198</span> Preparation of Protective Coating Film on Metal Alloy</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Rana%20Th.%20A.%20Al-rubaye">Rana Th. A. Al-rubaye</a> </p> <p class="card-text"><strong>Abstract:</strong></p> A novel chromium-free protective coating films based on a zeolite coating was growing onto a FeCrAlloy metal using in –situ hydrothermal method. The zeolite film was obtained using in-situ crystallization process that is capable of coating large surfaces with complex shape and in confined spaces has been developed. The zeolite coating offers an advantage of a high mechanical stability and thermal stability. The physico-chemical properties were investigated using X-ray diffraction (XRD), Electron microscopy (SEM), Energy Dispersive X–ray analysis (EDX) and Thermogravimetric Analysis (TGA). The transition from oxide-on-alloy wires to hydrothermally synthesised uniformly zeolite coated surfaces was followed using SEM and XRD. In addition, the robustness of the prepared coating was confirmed by subjecting these to thermal cycling (ambient to 550°C). <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=fecralloy" title="fecralloy">fecralloy</a>, <a href="https://publications.waset.org/abstracts/search?q=zsm-5%20zeolite" title=" zsm-5 zeolite"> zsm-5 zeolite</a>, <a href="https://publications.waset.org/abstracts/search?q=zeolite%20coatings" title=" zeolite coatings"> zeolite coatings</a>, <a href="https://publications.waset.org/abstracts/search?q=hydrothermal%20method" title=" hydrothermal method"> hydrothermal method</a> </p> <a href="https://publications.waset.org/abstracts/30792/preparation-of-protective-coating-film-on-metal-alloy" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/30792.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">396</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">197</span> Regenerated Cellulose Prepared by Using NaOH/Urea</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Lee%20Chiau%20Yeng">Lee Chiau Yeng</a>, <a href="https://publications.waset.org/abstracts/search?q=Norhayani%20Othman"> Norhayani Othman</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Regenerated cellulose fiber is fabricated in the NaOH/urea aqueous solution. In this work, cellulose is dissolved in 7 .wt% NaOH/12 .wt% urea in the temperature of -12 °C to prepare regenerated cellulose. Thermal and structure properties of cellulose and regenerated cellulose was compared and investigated by Field Emission Scanning Electron Microscopy (FeSEM), Fourier Transform Infrared Spectroscopy (FTIR), X-Ray Diffraction (XRD), Thermogravimetric analysis (TGA), and Differential Scanning Calorimetry. Results of FeSEM revealed that the regenerated cellulose fibers showed a more circular shape with irregular size due to fiber agglomeration. FTIR showed the difference in between the structure of cellulose and the regenerated cellulose fibers. In this case, regenerated cellulose fibers have a cellulose II crystalline structure with lower degree of crystallinity. Regenerated cellulose exhibited better thermal stability than the cellulose. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=regenerated%20cellulose" title="regenerated cellulose">regenerated cellulose</a>, <a href="https://publications.waset.org/abstracts/search?q=cellulose" title=" cellulose"> cellulose</a>, <a href="https://publications.waset.org/abstracts/search?q=NaOH" title=" NaOH"> NaOH</a>, <a href="https://publications.waset.org/abstracts/search?q=urea" title=" urea"> urea</a> </p> <a href="https://publications.waset.org/abstracts/19617/regenerated-cellulose-prepared-by-using-naohurea" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/19617.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">196</span> Antibacterial Activity of Nickel Oxide Composite Films with Chitosan/Polyvinyl Chloride/Polyethylene Glycol</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ali%20Garba%20Danjani">Ali Garba Danjani</a>, <a href="https://publications.waset.org/abstracts/search?q=Abdulrasheed%20Halliru%20Usman"> Abdulrasheed Halliru Usman</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Due to the rapidly increasing biological applications and antibacterial properties of versatile chitosan composites, the effects of chitosan/polyvinyl chloride composites film were investigated. Chitosan/polyvinyl chloride films were prepared by a casting method. Polyethylene glycol (PEG) was used as a plasticizer in the blending stage of film preparation. Characterizations of films were done by Scanning Electron microscopy (SEM), Fourier transforms infrared spectroscopy (FTIR), and thermogravimetric analyzer (TGA). Chitosan composites incorporation enhanced the antibacterial activity of chitosan films against Escherichia coli and Staphylococcus aureus. The composite film produced is proposed as packaging or coating material because of its flexibility, antibacterial efficacy, and good mechanical strength. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=chitosan" title="chitosan">chitosan</a>, <a href="https://publications.waset.org/abstracts/search?q=polymeric%20nanocomposites" title=" polymeric nanocomposites"> polymeric nanocomposites</a>, <a href="https://publications.waset.org/abstracts/search?q=antibacterial%20activity" title=" antibacterial activity"> antibacterial activity</a>, <a href="https://publications.waset.org/abstracts/search?q=polymer%20blend" title=" polymer blend"> polymer blend</a> </p> <a href="https://publications.waset.org/abstracts/159830/antibacterial-activity-of-nickel-oxide-composite-films-with-chitosanpolyvinyl-chloridepolyethylene-glycol" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/159830.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">100</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=thermogravimetric&page=2">2</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=thermogravimetric&page=3">3</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=thermogravimetric&page=4">4</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=thermogravimetric&page=5">5</a></li> <li class="page-item"><a class="page-link" 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