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polymerization</title> <meta name="description" content="Search results for: chemical polymerization"> <meta name="keywords" content="chemical polymerization"> <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 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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="chemical polymerization"> <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> 4710</div> </div> </div> </div> <h1 class="mt-3 mb-3 text-center" style="font-size:1.6rem;">Search results for: chemical polymerization</h1> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4710</span> Preparation and Characterization of Conductive Poly(N-Ethyl Aniline)/Kaolinite Composite Material by Chemical Polymerization</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hande%20Ta%C5%9Fdemir">Hande Taşdemir</a>, <a href="https://publications.waset.org/abstracts/search?q=Meral%20%C5%9Eahin"> Meral Şahin</a>, <a href="https://publications.waset.org/abstracts/search?q=Mehmet%20Sa%C3%A7ak"> Mehmet Saçak</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Conductive composite materials obtained by physical or chemical mixing of two or more components having conducting and insulating properties have been increasingly attracted. Kaolinite in kaolin clays is one of silicates with two layers of molecular sheets of (Si2O5)2− and [Al2(OH)4]2+ with the chemical composition Al2Si2O5(OH)4. The most abundant hydrophillic kaolinite is extensively used in industrial processes and therefore it is convenient for the preparation of organic/inorganic composites. In this study, conductive poly(N-ethylaniline)/kaolinite composite was prepared by chemical polymerization of N-ethyl aniline in the presence of kaolinite particles using ammonium persulfate as oxidant in aqueous acidic medium. Poly(N-ethylaniline) content and conductivity of composite prepared were systematically investigated as a function of polymerization conditions such as ammonium persulfate, N-ethyl aniline and HCl concentrations. Poly(N-ethylaniline) content and conductivity of composite increased with increasing oxidant and monomer concentrations up to 0.1 M and 0.2 M, respectively, and decreased at higher concentrations. The maximum yield of polymer in the composite (15.0%) and the highest conductivity value of the composite (5.0×10-5 S/cm) was achieved by polymerization for 2 hours at 20°C in HCl of 0.5 M. The structure, morphological analyses and thermal behaviours of poly(N-ethylaniline)/kaolinite composite were characterized by FTIR and XRD spectroscopy, SEM and TGA techniques. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=kaolinite" title="kaolinite">kaolinite</a>, <a href="https://publications.waset.org/abstracts/search?q=poly%28N-ethylaniline%29" title=" poly(N-ethylaniline)"> poly(N-ethylaniline)</a>, <a href="https://publications.waset.org/abstracts/search?q=conductive%20composite" title=" conductive composite"> conductive composite</a>, <a href="https://publications.waset.org/abstracts/search?q=chemical%20polymerization" title=" chemical polymerization"> chemical polymerization</a> </p> <a href="https://publications.waset.org/abstracts/8150/preparation-and-characterization-of-conductive-polyn-ethyl-anilinekaolinite-composite-material-by-chemical-polymerization" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/8150.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">292</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4709</span> Copolymers of Pyrrole and α,ω-Dithienyl Terminated Poly(ethylene glycol)</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Nesrin%20K%C3%B6ken">Nesrin Köken</a>, <a href="https://publications.waset.org/abstracts/search?q=Esin%20A.%20G%C3%BCvel"> Esin A. Güvel</a>, <a href="https://publications.waset.org/abstracts/search?q=Nilg%C3%BCn%20K%C4%B1z%C4%B1lcan"> Nilgün Kızılcan</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This work presents synthesis of α,ω-dithienyl terminated poly(ethylene glycol) (PEGTh) capable for further chain extension by either chemical or electrochemical polymerization. PEGTh was characterized by FTIR and 1H-NMR. Further, copolymerization of PEGTh and pyrrole (Py) was performed by chemical oxidative polymerization using ceric (IV) salt as an oxidant (PPy-PEGTh). PEG without end group modification was used directly to prepare copolymers with Py by Ce (IV) salt (PPy-PEG). Block copolymers with mole ratio of pyrrole to PEGTh (PEG) 50:1 and 10:1 were synthesized. The electrical conductivities of copolymers PPy-PEGTh and PPy-PEG were determined by four-point probe technique. Influence of the synthetic route and content of the insulating segment on conductivity and yield of the copolymers were investigated. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=chemical%20oxidative%20polymerization" title="chemical oxidative polymerization">chemical oxidative polymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=conducting%20polymer" title=" conducting polymer"> conducting polymer</a>, <a href="https://publications.waset.org/abstracts/search?q=poly%28ethylene%20glycol%29" title=" poly(ethylene glycol)"> poly(ethylene glycol)</a>, <a href="https://publications.waset.org/abstracts/search?q=polypyrrole" title=" polypyrrole"> polypyrrole</a> </p> <a href="https://publications.waset.org/abstracts/20954/copolymers-of-pyrrole-and-ao-dithienyl-terminated-polyethylene-glycol" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/20954.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">360</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">4708</span> Synthesis and Charaterization of Nanocomposite Poly (4,4' Methylenedianiline) Catalyzed by Maghnite-H+</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=A.%20Belmokhtar">A. Belmokhtar</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20Yahiaoui"> A. Yahiaoui</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20Benyoucef"> A. Benyoucef</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Belbachir"> M. Belbachir</a> </p> <p class="card-text"><strong>Abstract:</strong></p> We reported the synthesis and characterization of nanocomposite poly (4,4’ methylenedianiline) via chemical polymerization of monomers 4,4’ methylenedianiline by ammonium persulfate (APS) at room temperature catalyzed by Maghnite-H+. A facile method was demonstrated to grow poly (4,4’ methylenedianiline) nanocomposite, which was carried out by mixing Ammonium Persulfate (APS) aqueous and 4,4’ methylenedianiline solution in the presence of Maghnite-H+ at room temperature The effect of amount of catalyst and time on the polymerization yield of the polymers was studied. Structure was confirmed by elemental analysis, UV vis, RMN-1H, and voltammetry cyclique. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=charaterization" title="charaterization">charaterization</a>, <a href="https://publications.waset.org/abstracts/search?q=maghnite-h%2B" title=" maghnite-h+"> maghnite-h+</a>, <a href="https://publications.waset.org/abstracts/search?q=polymerization" title=" polymerization"> polymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=poly%20%284" title=" poly (4"> poly (4</a>, <a href="https://publications.waset.org/abstracts/search?q=4%E2%80%99%20methylenedianiline%29" title="4’ methylenedianiline)">4’ methylenedianiline)</a> </p> <a href="https://publications.waset.org/abstracts/30737/synthesis-and-charaterization-of-nanocomposite-poly-44-methylenedianiline-catalyzed-by-maghnite-h" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/30737.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">289</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">4707</span> Optimization of the Conditions of Oligomerization and Polymerization Processes of Selected Olefins with the Use of Complex Compounds of Transition Metal Ions</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Joanna%20Drze%C5%BCd%C5%BCon">Joanna Drzeżdżon</a>, <a href="https://publications.waset.org/abstracts/search?q=Marzena%20Bia%C5%82ek"> Marzena Białek</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Polyolefins are a group of materials used today in all areas of life. They are used in the food, domestic and other industries. In particular, polyethylene and polypropylene have found application in the production of packaging materials, pipes, containers, car parts as well as elements of medical equipment, e.g. syringes. Optimization of the polymerization and oligomerization processes of selected olefins is a very important stage before the technological implementation of polyolefin production. The purpose of the studies is to determine the conditions for ethylene polymerization as well as 3-buten-2-ol and 2-chloro-2-propen-1-ol oligomerization with the use of oxovanadium(IV) dipicolinate complexes with N-heterocyclic ligands. Additionally, the studies aims to determine the catalytic activities of the dipicolinate oxovanadium(IV) complexes with N-heterocyclic ligands in the studied polymerization and oligomerization processes. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=buten-2-ol" title="buten-2-ol">buten-2-ol</a>, <a href="https://publications.waset.org/abstracts/search?q=dipicolinate" title=" dipicolinate"> dipicolinate</a>, <a href="https://publications.waset.org/abstracts/search?q=ethylene" title=" ethylene"> ethylene</a>, <a href="https://publications.waset.org/abstracts/search?q=polymerization" title=" polymerization"> polymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=oligomerization" title=" oligomerization"> oligomerization</a>, <a href="https://publications.waset.org/abstracts/search?q=vanadium" title=" vanadium"> vanadium</a> </p> <a href="https://publications.waset.org/abstracts/142290/optimization-of-the-conditions-of-oligomerization-and-polymerization-processes-of-selected-olefins-with-the-use-of-complex-compounds-of-transition-metal-ions" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/142290.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">4706</span> Performance Comparison of Different Regression Methods for a Polymerization Process with Adaptive Sampling</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Florin%20Leon">Florin Leon</a>, <a href="https://publications.waset.org/abstracts/search?q=Silvia%20Curteanu"> Silvia Curteanu</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Developing complete mechanistic models for polymerization reactors is not easy, because complex reactions occur simultaneously; there is a large number of kinetic parameters involved and sometimes the chemical and physical phenomena for mixtures involving polymers are poorly understood. To overcome these difficulties, empirical models based on sampled data can be used instead, namely regression methods typical of machine learning field. They have the ability to learn the trends of a process without any knowledge about its particular physical and chemical laws. Therefore, they are useful for modeling complex processes, such as the free radical polymerization of methyl methacrylate achieved in a batch bulk process. The goal is to generate accurate predictions of monomer conversion, numerical average molecular weight and gravimetrical average molecular weight. This process is associated with non-linear gel and glass effects. For this purpose, an adaptive sampling technique is presented, which can select more samples around the regions where the values have a higher variation. Several machine learning methods are used for the modeling and their performance is compared: support vector machines, k-nearest neighbor, k-nearest neighbor and random forest, as well as an original algorithm, large margin nearest neighbor regression. The suggested method provides very good results compared to the other well-known regression algorithms. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=batch%20bulk%20methyl%20methacrylate%20polymerization" title="batch bulk methyl methacrylate polymerization">batch bulk methyl methacrylate polymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=adaptive%20sampling" title=" adaptive sampling"> adaptive sampling</a>, <a href="https://publications.waset.org/abstracts/search?q=machine%20learning" title=" machine learning"> machine learning</a>, <a href="https://publications.waset.org/abstracts/search?q=large%20margin%20nearest%20neighbor%20regression" title=" large margin nearest neighbor regression"> large margin nearest neighbor regression</a> </p> <a href="https://publications.waset.org/abstracts/54074/performance-comparison-of-different-regression-methods-for-a-polymerization-process-with-adaptive-sampling" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/54074.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">304</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">4705</span> Heterophase Polymerization of Pyrrole and Thienyl End Capped Ethoxylated Nonyl Phenol by Iron (III) Chloride</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=G%C3%B6rkem%20%C3%9Clk%C3%BC">Görkem Ülkü</a>, <a href="https://publications.waset.org/abstracts/search?q=Nesrin%20K%C3%B6ken"> Nesrin Köken</a>, <a href="https://publications.waset.org/abstracts/search?q=Esin%20A.%20G%C3%BCvel"> Esin A. Güvel</a>, <a href="https://publications.waset.org/abstracts/search?q=Nilg%C3%BCn%20K%C4%B1z%C4%B1lcan"> Nilgün Kızılcan</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Ethoxylated nonyl phenols (ENP) and ceric ammonium nitrate redox systems have been used for the polymerization of vinyl and acrylic monomers. In that case, ENP acted as an organic reducing agent in the presence of Ce (IV) salt and a radical was formed. The polymers obtained with that redox system contained ENP chain ends because the radicals are formed on the reducing molecules. Similar copolymer synthesis has been reported using poly(ethylene oxide) instead of its nonyl phenol terminated derivative, ENP. However, copolymers of poly(ethylene oxide) and conducting polymers synthesized by ferric ions were produced in two steps. Firstly, heteroatoms (pyrrole, thiophene etc.) were attached to the poly(ethylene oxide) chains then copolymerization with heterocyclic monomers was carried out. In this work, ethoxylated nonylphenol (ENP) was reacted with 2-thiophenecarbonyl chloride in order to synthesize a macromonomer containing thienyl end-group (ENP-ThC). Then, copolymers of ENP-ThC and pyrrole were synthesized by chemical oxidative polymerization using iron (III) chloride as an oxidant. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=end%20capped%20polymer" title="end capped polymer">end capped polymer</a>, <a href="https://publications.waset.org/abstracts/search?q=ethoxylated%20nonylphenol" title=" ethoxylated nonylphenol"> ethoxylated nonylphenol</a>, <a href="https://publications.waset.org/abstracts/search?q=heterophase%20polymerization" title=" heterophase polymerization"> heterophase polymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=polypyrrole" title=" polypyrrole"> polypyrrole</a> </p> <a href="https://publications.waset.org/abstracts/20937/heterophase-polymerization-of-pyrrole-and-thienyl-end-capped-ethoxylated-nonyl-phenol-by-iron-iii-chloride" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/20937.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">407</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">4704</span> Functionalization and Dispersion of Multiwall Carbon Nanotubes in Waterborne Polyurethane</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Shahla%20Hajializadeh">Shahla Hajializadeh</a>, <a href="https://publications.waset.org/abstracts/search?q=Maryam%20Hamedanlou"> Maryam Hamedanlou</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Multiwall carbon nanotubes were chemically modified with amide groups for the purpose of enhancing their chemical affinity with waterborne polyurethane. In this study, a thermoplastic nanocomposite containing functionalized multiwall carbon nanotube/waterborne polyurethane (WBPU/MWNT) via in situ polymerization has been prepared. The impacts of MWNT addition on the morphology and electrical properties of nanocomposites were investigated. Micrographs of Scanning Electron Microscopy (SEM) prove that functionalized CNT can be effectively dispersed in WBPU matrix. The electrical conductivity of nanocomposites increased with the CNT contents in as such the nanocomposites containing 1 wt% of MWNT exhibited a conductivity nearly five orders of magnitude higher than the WBPU film. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=chemical%20functionalization" title="chemical functionalization">chemical functionalization</a>, <a href="https://publications.waset.org/abstracts/search?q=electrical%20properties" title=" electrical properties"> electrical properties</a>, <a href="https://publications.waset.org/abstracts/search?q=in%20situ%20polymerization" title=" in situ polymerization"> in situ polymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=morphology" title=" morphology"> morphology</a>, <a href="https://publications.waset.org/abstracts/search?q=multiwall%20carbon%20nanotubes" title=" multiwall carbon nanotubes"> multiwall carbon nanotubes</a>, <a href="https://publications.waset.org/abstracts/search?q=waterborne%20polyurethane" title=" waterborne polyurethane"> waterborne polyurethane</a> </p> <a href="https://publications.waset.org/abstracts/55470/functionalization-and-dispersion-of-multiwall-carbon-nanotubes-in-waterborne-polyurethane" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/55470.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">266</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4703</span> Photopolymerization of Dimethacrylamide with (Meth)acrylates</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Yuling%20Xu">Yuling Xu</a>, <a href="https://publications.waset.org/abstracts/search?q=Haibo%20Wang"> Haibo Wang</a>, <a href="https://publications.waset.org/abstracts/search?q=Dong%20Xie"> Dong Xie</a> </p> <p class="card-text"><strong>Abstract:</strong></p> A photopolymerizable dimethacrylamide was synthesized and copolymerized with the selected (meth)acrylates. The polymerization rate, degree of conversion, gel time, and compressive strength of the formed neat resins were investigated. The results show that in situ photo-polymerization of the synthesized dimethacrylamide with comonomers having an electron-withdrawing and/or acrylate group dramatically increased the polymerization rate, degree of conversion, and compressive strength. On the other hand, an electron-donating group on either carbon-carbon double bond or the ester linkage slowed down the polymerization. In contrast, the triethylene glycol dimethacrylate-based system did not show a clear pattern. Both strong hydrogen-bonding between (meth)acrylamide and organic acid groups may be responsible for higher compressive strengths. Within the limitation of this study, the photo-polymerization of dimethacrylamide can be greatly accelerated by copolymerization with monomers having electron-withdrawing and/or acrylate groups. The monomers with methacrylate group can significantly reduce the polymerization rate and degree of conversion. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=photopolymerization" title="photopolymerization">photopolymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=dimethacrylamide" title=" dimethacrylamide"> dimethacrylamide</a>, <a href="https://publications.waset.org/abstracts/search?q=the%20degree%20of%20conversion" title=" the degree of conversion"> the degree of conversion</a>, <a href="https://publications.waset.org/abstracts/search?q=compressive%20strength" title=" compressive strength"> compressive strength</a> </p> <a href="https://publications.waset.org/abstracts/93577/photopolymerization-of-dimethacrylamide-with-methacrylates" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/93577.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">156</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">4702</span> Study of the Adsorption of Metal Ions Ag+ Mg2+, Ni2+ by the Chemical and Electrochemical Polydibenzoether Crown</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Dalila%20Chouder">Dalila Chouder</a>, <a href="https://publications.waset.org/abstracts/search?q=Djaafer%20Benachour"> Djaafer Benachour</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This work concerns the study of the adsorption of metal ions Ag +, Mg +, and Ni2+ in aqueous medium by polydibenzoether-ROWN based on three factors: Temperature, time and concentration. The polydibenzoether crown was synthesized by two means: Chemical and electrochemical. The behavior of the two polymers has been different, and turns out very interesting for chemical polydibenzoether crown has identified conditions. Chemical and électronique polydibenzoether crown have different extraction screw vi property of adsoption of ions fifférents, this study also shows that plyméres doped may have an advantageous electrical conductivity. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=polymerization" title="polymerization">polymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=electrochemical" title=" electrochemical"> electrochemical</a>, <a href="https://publications.waset.org/abstracts/search?q=conductivity" title=" conductivity"> conductivity</a>, <a href="https://publications.waset.org/abstracts/search?q=complexing%20metal%20ions" title=" complexing metal ions"> complexing metal ions</a> </p> <a href="https://publications.waset.org/abstracts/26255/study-of-the-adsorption-of-metal-ions-ag-mg2-ni2-by-the-chemical-and-electrochemical-polydibenzoether-crown" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/26255.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">264</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">4701</span> Rejuvenation of Aged Kraft-Cellulose Insulating Paper Used in Transformers</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Y.%20Jeon">Y. Jeon</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20Bissessur"> A. Bissessur</a>, <a href="https://publications.waset.org/abstracts/search?q=J.%20Lin"> J. Lin</a>, <a href="https://publications.waset.org/abstracts/search?q=P.%20Ndungu"> P. Ndungu</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Most transformers employ the usage of cellulose paper, which has been chemically modified through the Kraft process that acts as an effective insulator. Cellulose ageing and oil degradation are directly linked to fouling of the transformer and accumulation of large quantities of waste insulating paper. In addition to technical difficulties, this proves costly for power utilities to deal with. Currently there are no cost effective method for the rejuvenation of cellulose paper that has been documented nor proposed, since renewal of used insulating paper is implemented as the best option. This study proposes and contrasts different rejuvenation methods of accelerated aged cellulose insulating paper by chemical and bio-bleaching processes. Of the three bleaching methods investigated, two are, conventional chlorine-based sodium hypochlorite (m/v), and chlorine-free hydrogen peroxide (v/v), whilst the third is a bio-bleaching technique that uses a bacterium isolate, Acinetobacter strain V2. Through chemical bleaching, varying the strengths of the bleaching reagents at 0.3 %, 0.6 %, 0.9 %, 1.2 %, 1.5 % and 1.8 % over 4 hrs. were analyzed. Bio-bleaching implemented a bacterium isolate, Acinetobacter strain V2, to bleach the aged Kraft paper over 4 hrs. The determination of the amount of alpha cellulose, degree of polymerization and viscosity carried out on Kraft-cellulose insulating paper before and after bleaching. Overall the investigated techniques of chemical and bio-bleaching were successful and effective in treating degraded and accelerated aged Kraft-cellulose insulating paper, however, to varying extents. Optimum conditions for chemical bleaching were attained at bleaching strengths of 1.2 % (m/v) NaOCl and 1.5 % (v/v) H2O2 yielding alpha cellulose contents of 82.4 % and 80.7 % and degree of polymerizations of 613 and 616 respectively. Bio-bleaching using Acinetobacter strain V2 proved to be the superior technique with alpha cellulose levels of 89.0 % and a degree of polymerization of 620. Chemical bleaching techniques require careful and controlled clean-up treatments as it is chlorine and hydrogen peroxide based while bio-bleaching is an extremely eco-friendly technique. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=alpha%20cellulose" title="alpha cellulose">alpha cellulose</a>, <a href="https://publications.waset.org/abstracts/search?q=bio-bleaching" title=" bio-bleaching"> bio-bleaching</a>, <a href="https://publications.waset.org/abstracts/search?q=degree%20of%20polymerization" title=" degree of polymerization"> degree of polymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=Kraft-cellulose%20insulating%20paper" title=" Kraft-cellulose insulating paper"> Kraft-cellulose insulating paper</a>, <a href="https://publications.waset.org/abstracts/search?q=transformer" title=" transformer"> transformer</a>, <a href="https://publications.waset.org/abstracts/search?q=viscosity" title=" viscosity"> viscosity</a> </p> <a href="https://publications.waset.org/abstracts/30881/rejuvenation-of-aged-kraft-cellulose-insulating-paper-used-in-transformers" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/30881.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">270</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">4700</span> Highly Stretchable, Intelligent and Conductive PEDOT/PU Nanofibers Based on Electrospinning and in situ Polymerization</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Kun%20Qi">Kun Qi</a>, <a href="https://publications.waset.org/abstracts/search?q=Yuman%20Zhou"> Yuman Zhou</a>, <a href="https://publications.waset.org/abstracts/search?q=Jianxin%20He"> Jianxin He</a> </p> <p class="card-text"><strong>Abstract:</strong></p> A facile fabrication strategy via electrospinning and followed by in situ polymerization to fabricate a highly stretchable and conductive Poly(3,4-ethylenedioxythiophene)/Polyurethane (PEDOT/PU) nanofibrous membrane is reported. PU nanofibers were prepared by electrospinning and then PEDOT was coated on the plasma modified PU nanofiber surface via in-situ polymerization to form flexible PEDOT/PU composite nanofibers with conductivity. The results show PEDOT is successfully synthesized on the surface of PU nanofiber and PEDOT/PU composite nanofibers possess skin-core structure. Furthermore, the experiments indicate the optimal technological parameters of the polymerization process are as follow: The concentration of EDOT monomers is 50 mmol/L, the polymerization time is 24 h and the temperature is 25℃. The PEDOT/PU nanofibers exhibit excellent electrical conductivity ( 27.4 S/cm). In addition, flexible sensor made from conductive PEDOT/PU nanofibers shows highly sensitive response towards tensile strain and also can be used to detect finger motion. The results demonstrate promising application of the as-obtained nanofibrous membrane in flexible wearable electronic fields. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=electrospinning" title="electrospinning">electrospinning</a>, <a href="https://publications.waset.org/abstracts/search?q=polyurethane" title=" polyurethane"> polyurethane</a>, <a href="https://publications.waset.org/abstracts/search?q=PEDOT" title=" PEDOT"> PEDOT</a>, <a href="https://publications.waset.org/abstracts/search?q=conductive%20nanofiber" title=" conductive nanofiber"> conductive nanofiber</a>, <a href="https://publications.waset.org/abstracts/search?q=flexible%20senor" title=" flexible senor"> flexible senor</a> </p> <a href="https://publications.waset.org/abstracts/68101/highly-stretchable-intelligent-and-conductive-pedotpu-nanofibers-based-on-electrospinning-and-in-situ-polymerization" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/68101.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">359</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">4699</span> 2D CFD-PBM Coupled Model of Particle Growth in an Industrial Gas Phase Fluidized Bed Polymerization Reactor</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=H.%20Kazemi%20Esfeh">H. Kazemi Esfeh</a>, <a href="https://publications.waset.org/abstracts/search?q=V.%20Akbari"> V. Akbari</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Ehdaei"> M. Ehdaei</a>, <a href="https://publications.waset.org/abstracts/search?q=T.%20N.%20G.%20Borhani"> T. N. G. Borhani</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20Shamiri"> A. Shamiri</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Najafi"> M. Najafi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In an industrial fluidized bed polymerization reactor, particle size distribution (PSD) plays a significant role in the reactor efficiency evaluation. The computational fluid dynamic (CFD) models coupled with population balance equation (CFD-PBM) have been extensively employed to investigate the flow behavior in the poly-disperse multiphase fluidized bed reactors (FBRs) utilizing ANSYS Fluent code. In this study, an existing CFD-PBM/ DQMOM coupled modeling framework has been used to highlight its potential to analyze the industrial-scale gas phase polymerization reactor. The predicted results reveal an acceptable agreement with the observed industrial data in terms of pressure drop and bed height. The simulated results also indicate that the higher particle growth rate can be achieved for bigger particles. Hence, the 2D CFD-PBM/DQMOM coupled model can be used as a reliable tool for analyzing and improving the design and operation of the gas phase polymerization FBRs. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=computational%20fluid%20dynamics" title="computational fluid dynamics">computational fluid dynamics</a>, <a href="https://publications.waset.org/abstracts/search?q=population%20balance%20equation" title=" population balance equation"> population balance equation</a>, <a href="https://publications.waset.org/abstracts/search?q=fluidized%20bed%20polymerization%20reactor" title=" fluidized bed polymerization reactor"> fluidized bed polymerization reactor</a>, <a href="https://publications.waset.org/abstracts/search?q=direct%20quadrature%20method%20of%20moments" title=" direct quadrature method of moments"> direct quadrature method of moments</a> </p> <a href="https://publications.waset.org/abstracts/35644/2d-cfd-pbm-coupled-model-of-particle-growth-in-an-industrial-gas-phase-fluidized-bed-polymerization-reactor" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/35644.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">4698</span> Copolymers of Epsilon-Caprolactam Received via Anionic Polymerization in the Presence of Polypropylene Glycol Based Polymeric Activators</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Krasimira%20N.%20Zhilkova">Krasimira N. Zhilkova</a>, <a href="https://publications.waset.org/abstracts/search?q=Mariya%20K.%20Kyulavska"> Mariya K. Kyulavska</a>, <a href="https://publications.waset.org/abstracts/search?q=Roza%20P.%20Mateva"> Roza P. Mateva</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The anionic polymerization of -caprolactam (CL) with bifunctional activators has been extensively studied as an effective and beneficial method of improving chemical and impact resistances, elasticity and other mechanical properties of polyamide (PA6). In presence of activators or macroactivators (MAs) also called polymeric activators (PACs) the anionic polymerization of lactams proceeds rapidly at a temperature range of 130-180C, well below the melting point of PA-6 (220C) permitting thus the direct manufacturing of copolymer product together with desired modifications of polyamide properties. Copolymers of PA6 with an elastic polypropylene glycol (PPG) middle block into main chain were successfully synthesized via activated anionic ring opening polymerization (ROP) of CL. Using novel PACs based on PPG polyols (with differ molecular weight) the anionic ROP of CL was realized and investigated in the presence of a basic initiator sodium salt of CL (NaCL). The PACs were synthesized as N-carbamoyllactam derivatives of hydroxyl terminated PPG functionalized with isophorone diisocyanate [IPh, 5-Isocyanato-1-(isocyanatomethyl)-1,3,3-trimethylcyclohexane] and blocked then with CL units via an addition reaction. The block copolymers were analyzed and proved with 1H-NMR and FT-IR spectroscopy. The influence of the CL/PACs ratio in feed, the length of the PPG segments and polymerization conditions on the kinetics of anionic ROP, on average molecular weight, and on the structure of the obtained block copolymers were investigated. The structure and phase behaviour of the copolymers were explored with differential scanning calorimetry, wide-angle X-ray diffraction, thermogravimetric analysis and dynamic mechanical thermal analysis. The crystallinity dependence of PPG content incorporated into copolymers main backbone was estimate. Additionally, the mechanical properties of the obtained copolymers were studied by notched impact test. From the performed investigation in this study could be concluded that using PPG based PACs at the chosen ROP conditions leads to obtaining well-defined PA6-b-PPG-b-PA6 copolymers with improved impact resistance. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=anionic%20ring%20opening%20polymerization" title="anionic ring opening polymerization">anionic ring opening polymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=caprolactam" title=" caprolactam"> caprolactam</a>, <a href="https://publications.waset.org/abstracts/search?q=polyamide%20copolymers" title=" polyamide copolymers"> polyamide copolymers</a>, <a href="https://publications.waset.org/abstracts/search?q=polypropylene%20glycol" title=" polypropylene glycol"> polypropylene glycol</a> </p> <a href="https://publications.waset.org/abstracts/21195/copolymers-of-epsilon-caprolactam-received-via-anionic-polymerization-in-the-presence-of-polypropylene-glycol-based-polymeric-activators" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/21195.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">415</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">4697</span> Chromatographic Preparation and Performance on Zinc Ion Imprinted Monolithic Column and Its Adsorption Property</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=X.%20Han">X. Han</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20Duan"> S. Duan</a>, <a href="https://publications.waset.org/abstracts/search?q=C.%20Liu"> C. Liu</a>, <a href="https://publications.waset.org/abstracts/search?q=C.%20Zhou"> C. Zhou</a>, <a href="https://publications.waset.org/abstracts/search?q=W.%20Zhu"> W. Zhu</a>, <a href="https://publications.waset.org/abstracts/search?q=L.%20Kong"> L. Kong</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The ionic imprinting technique refers to the three-dimensional rigid structure with the fixed pore sizes, which was formed by the binding interactions of ions and functional monomers and used ions as the template, it has a high level of recognition to the ionic template. The preparation of monolithic column by the in-situ polymerization need to put the compound of template, functional monomers, cross-linking agent and initiating agent into the solution, dissolve it and inject to the column tube, and then the compound will have a polymerization reaction at a certain temperature, after the synthetic reaction, we washed out the unread template and solution. The monolithic columns are easy to prepare, low consumption and cost-effective with fast mass transfer, besides, they have many chemical functions. But the monolithic columns have some problems in the practical application, such as low-efficiency, quantitative analysis cannot be performed accurately because of the peak shape is wide and has tailing phenomena; the choice of polymerization systems is limited and the lack of theoretical foundations. Thus the optimization of components and preparation methods is an important research direction. During the preparation of ionic imprinted monolithic columns, pore-forming agent can make the polymer generate the porous structure, which can influence the physical properties of polymer, what’ s more, it can directly decide the stability and selectivity of polymerization reaction. The compounds generated in the pre-polymerization reaction could directly decide the identification and screening capabilities of imprinted polymer; thus the choice of pore-forming agent is quite critical in the preparation of imprinted monolithic columns. This article mainly focuses on the research that when using different pore-forming agents, the impact of zinc ion imprinted monolithic column on the enrichment performance of zinc ion. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=high%20performance%20liquid%20chromatography%20%28HPLC%29" title="high performance liquid chromatography (HPLC)">high performance liquid chromatography (HPLC)</a>, <a href="https://publications.waset.org/abstracts/search?q=ionic%20imprinting" title=" ionic imprinting"> ionic imprinting</a>, <a href="https://publications.waset.org/abstracts/search?q=monolithic%20column" title=" monolithic column"> monolithic column</a>, <a href="https://publications.waset.org/abstracts/search?q=pore-forming%20agent" title=" pore-forming agent"> pore-forming agent</a> </p> <a href="https://publications.waset.org/abstracts/82128/chromatographic-preparation-and-performance-on-zinc-ion-imprinted-monolithic-column-and-its-adsorption-property" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/82128.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">214</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">4696</span> Synthesis, Characterization and Impedance Analysis of Polypyrrole/La0.7Ca0.3MnO3 Nanocomposites</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=M.%20G.%20Smitha">M. G. Smitha</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20V.%20Murugendrappa"> M. V. Murugendrappa</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Perovskite manganite La<sub>0.7</sub>Ca<sub>0.3</sub>MnO<sub>3</sub> was synthesized by Sol-gel method. Polymerization of pyrrole was carried by in-situ polymerization method. The composite of pyrrole (Py)/La<sub>0.7</sub>Ca<sub>0.3</sub>MnO<sub>3</sub> composite in the presence of oxidizing agent ammonium per sulphate to synthesize polypyrrole (PPy)/La<sub>0.7</sub>Ca<sub>0.3</sub>MnO<sub>3</sub> (LCM) composite was carried out by the same in-situ polymerization method. The PPy/LCM composites were synthesized with varying compositions like 10, 20, 30, 40, and 50 wt.% of LCM in Py. The surface morphologies of these composites were analyzed by using scanning electron microscope (SEM). The images show that LCM particles are embedded in PPy chain. The impedance measurement of PPy/LCM at different temperature ranges from 30 to 180 °C was studied using impedance analyzer. The study shows that impedance is frequency and temperature dependent and it is found to decrease with increase in frequency and temperature. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=polypyrrole" title="polypyrrole">polypyrrole</a>, <a href="https://publications.waset.org/abstracts/search?q=sol%20gel" title=" sol gel"> sol gel</a>, <a href="https://publications.waset.org/abstracts/search?q=impedance" title=" impedance"> impedance</a>, <a href="https://publications.waset.org/abstracts/search?q=composites" title=" composites"> composites</a> </p> <a href="https://publications.waset.org/abstracts/62179/synthesis-characterization-and-impedance-analysis-of-polypyrrolela07ca03mno3-nanocomposites" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/62179.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">375</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">4695</span> Synthesis and Study of Properties of Polyaniline/Nickel Sulphide Nanocomposites</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Okpaneje%20Onyinye%20Theresa">Okpaneje Onyinye Theresa</a>, <a href="https://publications.waset.org/abstracts/search?q=Ugwu%20Laeticia%20Udodiri"> Ugwu Laeticia Udodiri</a>, <a href="https://publications.waset.org/abstracts/search?q=Okereke%20Ngozi%20Agatha"> Okereke Ngozi Agatha</a>, <a href="https://publications.waset.org/abstracts/search?q=Okoli%20Nonso%20Livinus"> Okoli Nonso Livinus</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This work is on the synthesis and study of the optical characterization of polyaniline/nickel sulphide nanocomposite. Polyaniline (PANI) and nickel sulphide (NiS) nanoparticles were synthesized by oxidative chemical polymerization and sol-gel method. The polyaniline nickel sulphide nanocomposites with various concentrations of NiS were synthesized by in-situ polymerization of aniline monomer. In each case, the nickel sulphide nanoparticles were uniformly dispersed in the aniline hydrochloride before the initiation of oxidative chemical polymerization using ammonium persulphate. The samples formed were subjected to optical characterization using an ultraviolet (UV)-visible light (VIS) spectrophotometer (model: 756S UV – VIS). Optical analysis of the synthesized nanoparticles and nanocomposites showed absorption of radiation within VIS regions. The Tauc model was used to obtain the optical band gap. Energy band gap values of PANI and NiS were found to be 2.50 eV and 1.95 eV, respectively. PANI/NiSnanocomposites has an energy band gap that decreased from 2.25 eV to 1.90 eV as the amount of NiS increased (from 0.5g to 2.0g). These optical results showed that these nanocomposites are potential materials to be considered in solar cells and optoelectronics devices. The structural analysis confirmed the formation of polyaniline and hexagonal nickel sulphide with an average crystallite size of 25.521 nm, while average crystallite sizes of PANI/NiSnanocomposites ranged from 19.458 nm to 25.108 nm. Average particle sizes obtained from the SEM images ranged from 23.24 nm to 51.88 nm. Compositional results confirmed the presence of desired elements that made up the nanoparticles and nanocomposites. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=polyaniline" title="polyaniline">polyaniline</a>, <a href="https://publications.waset.org/abstracts/search?q=nickel%20sulphide" title=" nickel sulphide"> nickel sulphide</a>, <a href="https://publications.waset.org/abstracts/search?q=polyaniline-nickel%20sulphide%20nanocomposite" title=" polyaniline-nickel sulphide nanocomposite"> polyaniline-nickel sulphide nanocomposite</a>, <a href="https://publications.waset.org/abstracts/search?q=optical%20characterization" title=" optical characterization"> optical characterization</a>, <a href="https://publications.waset.org/abstracts/search?q=structural%20analysis" title=" structural analysis"> structural analysis</a>, <a href="https://publications.waset.org/abstracts/search?q=morphological%20properties" title=" morphological properties"> morphological properties</a>, <a href="https://publications.waset.org/abstracts/search?q=compositional%20properties" title=" compositional properties"> compositional properties</a> </p> <a href="https://publications.waset.org/abstracts/153743/synthesis-and-study-of-properties-of-polyanilinenickel-sulphide-nanocomposites" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/153743.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">4694</span> Rational Design and Synthesis of 2D/3D Conjugated Porous Polymers via Facile and 'Greener' Direct Arylation Polycondensation</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hassan%20Bohra">Hassan Bohra</a>, <a href="https://publications.waset.org/abstracts/search?q=Mingfeng%20Wang"> Mingfeng Wang</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Conjugated porous polymers (CPPs) are amorphous, insoluble and highly robust organic semiconductors that have been largely synthesized by traditional transition-metal catalyzed reactions. The distinguishing feature of CPP materials is that they combine microporosity and high surface areas with extended conjugation, making them ideal for versatile applications such as separation, catalysis and energy storage. By applying a modular approach to synthesis, chemical and electronic properties of CPPs can be tailored for specific applications making these materials economical alternatives to inorganic semiconductors. Direct arylation - an environmentally benign alternative to traditional polymerization reactions – is one such reaction that extensively over the last decade for the synthesis of linear p-conjugated polymers. In this report, we present the synthesis and characterization of a new series of robust conjugated porous polymers synthesized by facile direct arylation polymerization of thiophene-flanked acceptor building blocks with multi-brominated aryls with different geometries. We observed that the porosities and morphologies of the polymers are determined by the chemical structure of the aryl bromide used. Moreover, good control of the optical bandgap in the range 2.53 - 1.3 eV could be obtained by using different building blocks. Structure-property relationships demonstrated in this study suggest that direct arylation polymerization is an attractive synthetic tool for the rational design of porous organic materials with tunable photo-physical properties for applications in photocatalysis, energy storage and conversion. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=direct%20arylation" title="direct arylation">direct arylation</a>, <a href="https://publications.waset.org/abstracts/search?q=conjugated%20porous%20polymers" title=" conjugated porous polymers"> conjugated porous polymers</a>, <a href="https://publications.waset.org/abstracts/search?q=triazine" title=" triazine"> triazine</a>, <a href="https://publications.waset.org/abstracts/search?q=photocatalysis" title=" photocatalysis"> photocatalysis</a> </p> <a href="https://publications.waset.org/abstracts/84763/rational-design-and-synthesis-of-2d3d-conjugated-porous-polymers-via-facile-and-greener-direct-arylation-polycondensation" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/84763.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">294</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">4693</span> Optical Properties of N-(Hydroxymethyl) Acrylamide Polymer Gel Dosimeters for Radiation Therapy</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Khalid%20A.%20Rabaeh">Khalid A. Rabaeh</a>, <a href="https://publications.waset.org/abstracts/search?q=Belal%20Moftah"> Belal Moftah</a>, <a href="https://publications.waset.org/abstracts/search?q=Ahmed%20A.%20Basfar"> Ahmed A. Basfar</a>, <a href="https://publications.waset.org/abstracts/search?q=Akram%20A.%20Almousa"> Akram A. Almousa</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Polymer gel dosimeters are tissue equivalent martial that fabricated from radiation sensitive chemicals which, upon irradiation, polymerize as a function of absorbed radiation dose. Polymer gel dosimeters can uniquely record the radiation dose distribution in three-dimensions (3D). A novel composition of normoxic polymer gel dosimeters based on radiation-induced polymerization of N-(Hydroxymethyl)acrylamide (NHMA) is introduced in this study for radiotherapy treatment planning. The dosimeters were irradiated by 10 MV photon beam of a medical linear accelerator at a constant dose rate of 600 cGy/min with doses up to 30 Gy. The polymerization degree is directly proportional to absorbed dose received by the polymer gel. UV/Vis spectrophotometer was used to investigate the degree of white color of irradiated NHMA gel which is associated to the degree of polymerization of polymer gel dosimeters. The absorbance increases with absorbed dose for all gel dosimeters in the dose range between 0 and 30 Gy. Dose rate , energy of radiation and the stability of the polymerization after irradiation were investigated. No appreciable effects of these parameters on the performance of the novel gel dosimeters were observed. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=dosimeter" title="dosimeter">dosimeter</a>, <a href="https://publications.waset.org/abstracts/search?q=gel" title=" gel"> gel</a>, <a href="https://publications.waset.org/abstracts/search?q=spectrophotometer" title=" spectrophotometer"> spectrophotometer</a>, <a href="https://publications.waset.org/abstracts/search?q=N-%28Hydroxymethyl%29acrylamide" title=" N-(Hydroxymethyl)acrylamide "> N-(Hydroxymethyl)acrylamide </a> </p> <a href="https://publications.waset.org/abstracts/34646/optical-properties-of-n-hydroxymethyl-acrylamide-polymer-gel-dosimeters-for-radiation-therapy" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/34646.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">469</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4692</span> Use Process Ring-Opening Polymerization to Melt Processing of Cellulose Nanowhisker from Coconut Husk Fibers-Filled Polylactide-Based Nanocomposites</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Imam%20Wierawansyah%20Eltara">Imam Wierawansyah Eltara</a>, <a href="https://publications.waset.org/abstracts/search?q=Iftitah"> Iftitah</a>, <a href="https://publications.waset.org/abstracts/search?q=Agus%20Ismail"> Agus Ismail</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In the present work, cellulose nanowhiskers (CNW) extracted from coconut husk fibers, were incorporated in polylactide (PLA)-based composites. Prior to the blending, PLA chains were chemically grafted on the surface of CNW to enhance the compatibilization between CNW and the hydrophobic polyester matrix. Ring-opening polymerization of L-lactide was initiated from the hydroxyl groups available at the CNW surface to yield CNW-g-PLA nanohybrids. PLA-based nanocomposites were prepared by melt blending to ensure a green concept of the study thereby limiting the use of organic solvents. The influence of PLA-grafted cellulose nanoparticles on the mechanical and thermal properties of the ensuing nanocomposites was deeply investigated. The thermal behavior and mechanical properties of the nanocomposites were determined using differential scanning calorimetry (DSC) and dynamical mechanical and thermal analysis (DMTA), respectively. In theory, evidenced that the chemical grafting of CNW enhances their compatibility with the polymeric matrix and thus improves the final properties of the nanocomposites. Large modification of the crystalline properties such as the crystallization half-time was evidenced according to the nature of the PLA matrix and the content of nanofillers. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=cellulose%20nanowhiskers" title="cellulose nanowhiskers">cellulose nanowhiskers</a>, <a href="https://publications.waset.org/abstracts/search?q=nanocomposites" title=" nanocomposites"> nanocomposites</a>, <a href="https://publications.waset.org/abstracts/search?q=coconut%20husk%20fiber" title=" coconut husk fiber"> coconut husk fiber</a>, <a href="https://publications.waset.org/abstracts/search?q=ring%20opening%20polymerization" title=" ring opening polymerization"> ring opening polymerization</a> </p> <a href="https://publications.waset.org/abstracts/43287/use-process-ring-opening-polymerization-to-melt-processing-of-cellulose-nanowhisker-from-coconut-husk-fibers-filled-polylactide-based-nanocomposites" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/43287.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">317</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">4691</span> Direct In-Situ Ring Opening Polymerization of E-caprolactone to Produce Biodegradable PCL/Montmorillonite Nanocomposites</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Amine%20Harrane">Amine Harrane</a>, <a href="https://publications.waset.org/abstracts/search?q=Mahmoud%20Belalia"> Mahmoud Belalia</a> </p> <p class="card-text"><strong>Abstract:</strong></p> During the last decade, polymer layered silicate nanocomposites have received increasing attention from scientists and industrial researchers because they generally exhibit greatly improved mechanical, thermal, barrier and flame-retardant properties at low clay content in comparison with unfilled polymers or more conventional micro composites. Poly(ε-caprolactone) (PCL)-layered silicate nanocomposites have the advantage of adding biocompatibility and biodegradability to the traditional properties of nanocomposites. They can be prepared by in situ ring-opening polymerization of ε-caprolactone using a conventional initiator to induce polymerization in the presence of an organophilic clay, such as organomodified montmorillonite. Messersmith and Giannelis used montmorillonite exchanged with protonated 12-amino dodecanoic acid and Cr3+ exchanged fluorohectorite, a synthetic mica type of silicate. Sn-based catalysts such as tin (II) octoate and dibutyltin (IV) dimethoxide have been reported to efficiently promote the polymerization of ε-caprolactone in the presence of organomodified clays. In this work, we have used an alternative method to prepare PCL/montmorillonite nanocomposites. The cationic polymerization of ε-caprolactone was initiated directly by Maghnite-TOA, organomodified montmorillonite clay, to produce nanocomposites (Scheme 1). Resulted from nanocomposites were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), force atomic microscopy (AFM) and thermogravimetry. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=polycaprolactone" title="polycaprolactone">polycaprolactone</a>, <a href="https://publications.waset.org/abstracts/search?q=polycaprolactone%2Fclay%20nanocomposites" title=" polycaprolactone/clay nanocomposites"> polycaprolactone/clay nanocomposites</a>, <a href="https://publications.waset.org/abstracts/search?q=biodegradables%20nanocomposites" title=" biodegradables nanocomposites"> biodegradables nanocomposites</a>, <a href="https://publications.waset.org/abstracts/search?q=Maghnite" title=" Maghnite"> Maghnite</a>, <a href="https://publications.waset.org/abstracts/search?q=Insitu%20polymeriation" title=" Insitu polymeriation"> Insitu polymeriation</a> </p> <a href="https://publications.waset.org/abstracts/163797/direct-in-situ-ring-opening-polymerization-of-e-caprolactone-to-produce-biodegradable-pclmontmorillonite-nanocomposites" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/163797.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">78</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4690</span> Modeling of Polyethylene Particle Size Distribution in Fluidized Bed Reactors</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=R.%20Marandi">R. Marandi</a>, <a href="https://publications.waset.org/abstracts/search?q=H.%20Shahrir"> H. Shahrir</a>, <a href="https://publications.waset.org/abstracts/search?q=T.%20Nejad%20Ghaffar%20Borhani"> T. Nejad Ghaffar Borhani</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Kamaruddin"> M. Kamaruddin</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In the present study, a steady state population balance model was developed to predict the polymer particle size distribution (PSD) in ethylene gas phase fluidized bed olefin polymerization reactors. The multilayer polymeric flow model (MPFM) was used to calculate the growth rate of a single polymer particle under intra-heat and mass transfer resistance. The industrial plant data were used to calculate the growth rate of polymer particle and the polymer PSD. Numerical simulations carried out to describe the influence of effective monomer diffusion coefficient, polymerization rate and initial catalyst size on the catalyst particle growth and final polymer PSD. The results present that the intra-heat and mass limitation is important for the ethylene polymerization, the growth rate of particle and the polymer PSD in the fluidized bed reactor. The effect of the agglomeration on the PSD is also considered. The result presents that the polymer particle size distribution becomes broader as the agglomeration exits. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=population%20balance" title="population balance">population balance</a>, <a href="https://publications.waset.org/abstracts/search?q=olefin%20polymerization" title=" olefin polymerization"> olefin polymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=fluidized%20bed%20reactor" title=" fluidized bed reactor"> fluidized bed reactor</a>, <a href="https://publications.waset.org/abstracts/search?q=particle%20size%20distribution" title=" particle size distribution"> particle size distribution</a>, <a href="https://publications.waset.org/abstracts/search?q=agglomeration" title=" agglomeration"> agglomeration</a> </p> <a href="https://publications.waset.org/abstracts/35596/modeling-of-polyethylene-particle-size-distribution-in-fluidized-bed-reactors" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/35596.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">4689</span> Polymerization of Epsilon-Caprolactone Using Lipase Enzyme for Medical Applications</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Sukanya%20Devi%20Ramachandran">Sukanya Devi Ramachandran</a>, <a href="https://publications.waset.org/abstracts/search?q=Vaishnavi%20Muralidharan"> Vaishnavi Muralidharan</a>, <a href="https://publications.waset.org/abstracts/search?q=Kavya%20Chandrasekaran"> Kavya Chandrasekaran</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Polycaprolactone is polymer belonging to the polyester family that has noticeable characteristics of biodegradability and biocompatibility which is essential for medical applications. Polycaprolactone is produced by the ring opening polymerization of the monomer epsilon-Caprolactone (ε-CL) which is a closed ester, comprising of seven-membered ring. This process is normally catalysed by metallic components such as stannous octoate. It is difficult to remove the catalysts after the reaction, and they are also toxic to the human body. An alternate route of using enzymes as catalysts is being employed to reduce the toxicity. Lipase enzyme is a subclass of esterase that can easily attack the ester bonds of ε-CL. This research paper throws light on the extraction of lipase from germinating sunflower seeds and the activity of the biocatalyst in the polymerization of ε-CL. Germinating Sunflower seeds were crushed with fine sand in phosphate buffer of pH 6.5 into a fine paste which was centrifuged at 5000rpm for 10 minutes. The clear solution of the enzyme was tested for activity at various pH ranging from 5 to 7 and temperature ranging from 40oC to 70oC. The enzyme was active at pH6.0 and at 600C temperature. Polymerization of ε-CL was done using toluene as solvent with the catalysis of lipase enzyme, after which chloroform was added to terminate the reaction and was washed in cold methanol to obtain the polymer. The polymerization was done by varying the time from 72 hours to 6 days and tested for the molecular weight and the conversion of the monomer. The molecular weight obtained at 6 days is comparably higher. This method will be very effective, economical and eco-friendly to produce as the enzyme used can be regenerated as such at the end of the reaction and can be reused. The obtained polymers can be used for drug delivery and other medical applications. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=lipase" title="lipase">lipase</a>, <a href="https://publications.waset.org/abstracts/search?q=monomer" title=" monomer"> monomer</a>, <a href="https://publications.waset.org/abstracts/search?q=polycaprolactone" title=" polycaprolactone"> polycaprolactone</a>, <a href="https://publications.waset.org/abstracts/search?q=polymerization" title=" polymerization"> polymerization</a> </p> <a href="https://publications.waset.org/abstracts/85799/polymerization-of-epsilon-caprolactone-using-lipase-enzyme-for-medical-applications" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/85799.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">296</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">4688</span> From Homogeneous to Phase Separated UV-Cured Interpenetrating Polymer Networks: Influence of the System Composition on Properties and Microstructure</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Caroline%20Rocco">Caroline Rocco</a>, <a href="https://publications.waset.org/abstracts/search?q=Feyza%20Karasu"> Feyza Karasu</a>, <a href="https://publications.waset.org/abstracts/search?q=C%C3%A9line%20Croutx%C3%A9-Barghorn"> Céline Croutxé-Barghorn</a>, <a href="https://publications.waset.org/abstracts/search?q=Xavier%20Allonas"> Xavier Allonas</a>, <a href="https://publications.waset.org/abstracts/search?q=Maxime%20Lecomp%C3%A8re"> Maxime Lecompère</a>, <a href="https://publications.waset.org/abstracts/search?q=G%C3%A9rard%20Riess"> Gérard Riess</a>, <a href="https://publications.waset.org/abstracts/search?q=Yujing%20Zhang"> Yujing Zhang</a>, <a href="https://publications.waset.org/abstracts/search?q=Catarina%20Esteves"> Catarina Esteves</a>, <a href="https://publications.waset.org/abstracts/search?q=Leendert%20van%20der%20Ven"> Leendert van der Ven</a>, <a href="https://publications.waset.org/abstracts/search?q=Rolf%20van%20Benthem%20Gijsbertus%20de%20With"> Rolf van Benthem Gijsbertus de With</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Acrylates are widely used in UV-curing technology. Their high reactivity can, however, limit their conversion due to early vitrification. In addition, the free radical photopolymerization is known to be sensitive to oxygen inhibition leading to tacky surfaces. Although epoxides can lead to full polymerization, they are sensitive to humidity and exhibit low polymerization rate. To overcome the intrinsic limitations of both classes of monomers, Interpenetrating Polymer Networks (IPNs) can be synthesized. They consist of at least two cross linked polymers which are permanently entangled. They can be achieved under thermal and/or light induced polymerization in one or two steps approach. IPNs can display homogeneous to heterogeneous morphologies with various degrees of phase separation strongly linked to the monomer miscibility and also synthesis parameters. In this presentation, we synthesize UV-cured methacrylate - epoxide based IPNs with different chemical compositions in order to get a better understanding of their formation and phase separation. Miscibility before and during the photopolymerization, reaction kinetics, as well as mechanical properties and morphology have been investigated. The key parameters controlling the morphology and the phase separation, namely monomer miscibility and synthesis parameters have been identified. By monitoring the stiffness changes on the film surface, atomic force acoustic microscopy (AFAM) gave, in conjunction with polymerization kinetic profiles and thermomechanical properties, explanations and corroborated the miscibility predictions. When varying the methacrylate / epoxide ratio, it was possible to move from a miscible and highly-interpenetrated IPN to a totally immiscible and phase-separated one. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=investigation%20of%20properties%20and%20morphology" title="investigation of properties and morphology">investigation of properties and morphology</a>, <a href="https://publications.waset.org/abstracts/search?q=kinetics" title=" kinetics"> kinetics</a>, <a href="https://publications.waset.org/abstracts/search?q=phase%20separation" title=" phase separation"> phase separation</a>, <a href="https://publications.waset.org/abstracts/search?q=UV-cured%20IPNs" title=" UV-cured IPNs"> UV-cured IPNs</a> </p> <a href="https://publications.waset.org/abstracts/27489/from-homogeneous-to-phase-separated-uv-cured-interpenetrating-polymer-networks-influence-of-the-system-composition-on-properties-and-microstructure" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/27489.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">4687</span> Micro-Arc Oxidation Titanium and Post Treatment by Cold Plasma and Graft Polymerization of Acrylic Acid for Biomedical Application</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Shu-Chuan%20Liao">Shu-Chuan Liao</a>, <a href="https://publications.waset.org/abstracts/search?q=Chia-Ti%20Chang"> Chia-Ti Chang</a>, <a href="https://publications.waset.org/abstracts/search?q=Ko-Shao%20Chen"> Ko-Shao Chen</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Titanium and its alloy are widely used in many fields such as dentistry or orthopaedics. Due to their high strength low elastic modulus that chemical inertness and bio inert. The micro-arc oxidation used to formation a micro porous ceramic oxide layer film on Titanium surface and also to improve the resistance corrosion. For improving the biocompatibility, micro-arc oxidation surfaces bio-inert need to introduce reactive group. We introduced boundary layer by used plasma enhanced chemical vapor deposition of hexamethyldisilazane (HMDS) and organic active layer by UV light graft reactive monomer acrylic acid (AAc) therefore we can immobilize Chondroitin sulphate on surface easily by crosslinking EDC/NHS. The surface properties and composition of the modified layer were measured by scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) and water contact angle. Water contact angle of the plasma-treated Ti surface decreases from 60° to 38°, which is an indication of hydrophilicity. The results of electrochemical polarization analysis showed that the sample plasma treated at micro-arc oxidation after plasma treatment has the best corrosion resistance. The result showed that we can immobilize chondroitin sulfate successful by a series of modification and MTT assay indicated the biocompatibility has been improved in this study. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=MAO" title="MAO">MAO</a>, <a href="https://publications.waset.org/abstracts/search?q=plasma" title=" plasma"> plasma</a>, <a href="https://publications.waset.org/abstracts/search?q=graft%20polymerization" title=" graft polymerization"> graft polymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=biomedical%20application" title=" biomedical application"> biomedical application</a> </p> <a href="https://publications.waset.org/abstracts/43159/micro-arc-oxidation-titanium-and-post-treatment-by-cold-plasma-and-graft-polymerization-of-acrylic-acid-for-biomedical-application" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/43159.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">258</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">4686</span> Ag and Au Nanoparticles Fabrication in Cross-Linked Polymer Microgels for Their Comparative Catalytic Study</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Luqman%20Ali%20Shah">Luqman Ali Shah</a>, <a href="https://publications.waset.org/abstracts/search?q=Murtaza%20Sayed"> Murtaza Sayed</a>, <a href="https://publications.waset.org/abstracts/search?q=Mohammad%20Siddiq"> Mohammad Siddiq</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Three-dimensional cross-linked polymer microgels with temperature responsive N-isopropyl acrylamide (NIPAM) and pH-sensitive methacrylic acid (MAA) were successfully synthesized by free radical emulsion polymerization with different amount of MAA. Silver and gold nanoparticles with size of 6.5 and 3.5 nm (±0.5 nm) respectively were homogeneously reduced inside these materials by chemical reduction method at pH 2.78 and 8.36 for the preparation of hybrid materials. The samples were characterized by FTIR, DLS and TEM techniques. The catalytic activity of the hybrid materials was investigated for the reduction of 4-nitrophenol (4- NP) using NaBH4 as reducing agent by UV-visible spectroscopy. The hybrid polymer network synthesized at pH 8.36 shows enhanced catalytic efficiency compared to catalysts synthesized at pH 2.78. In this study, it has been explored that catalyst activity strongly depends on amount of MAA, synthesis pH and type of metal nanoparticles entrapped. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=cross-linked%20polymer%20microgels" title="cross-linked polymer microgels">cross-linked polymer microgels</a>, <a href="https://publications.waset.org/abstracts/search?q=free%20radical%20polymerization" title=" free radical polymerization"> free radical polymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=metal%20nanoparticles" title=" metal nanoparticles"> metal nanoparticles</a>, <a href="https://publications.waset.org/abstracts/search?q=catalytic%20activity" title=" catalytic activity"> catalytic activity</a>, <a href="https://publications.waset.org/abstracts/search?q=comparative%20study" title=" comparative study"> comparative study</a> </p> <a href="https://publications.waset.org/abstracts/60410/ag-and-au-nanoparticles-fabrication-in-cross-linked-polymer-microgels-for-their-comparative-catalytic-study" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/60410.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">323</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">4685</span> Forecast of Polyethylene Properties in the Gas Phase Polymerization Aided by Neural Network</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Nasrin%20Bakhshizadeh">Nasrin Bakhshizadeh</a>, <a href="https://publications.waset.org/abstracts/search?q=Ashkan%20Forootan"> Ashkan Forootan</a> </p> <p class="card-text"><strong>Abstract:</strong></p> A major problem that affects the quality control of polymer in the industrial polymerization is the lack of suitable on-line measurement tools to evaluate the properties of the polymer such as melt and density indices. Controlling the polymerization in ordinary method is performed manually by taking samples, measuring the quality of polymer in the lab and registry of results. This method is highly time consuming and leads to producing large number of incompatible products. An online application for estimating melt index and density proposed in this study is a neural network based on the input-output data of the polyethylene production plant. Temperature, the level of reactors' bed, the intensity of ethylene mass flow, hydrogen and butene-1, the molar concentration of ethylene, hydrogen and butene-1 are used for the process to establish the neural model. The neural network is taught based on the actual operational data and back-propagation and Levenberg-Marquart techniques. The simulated results indicate that the neural network process model established with three layers (one hidden layer) for forecasting the density and the four layers for the melt index is able to successfully predict those quality properties. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=polyethylene" title="polyethylene">polyethylene</a>, <a href="https://publications.waset.org/abstracts/search?q=polymerization" title=" polymerization"> polymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=density" title=" density"> density</a>, <a href="https://publications.waset.org/abstracts/search?q=melt%20index" title=" melt index"> melt index</a>, <a href="https://publications.waset.org/abstracts/search?q=neural%20network" title=" neural network"> neural network</a> </p> <a href="https://publications.waset.org/abstracts/105904/forecast-of-polyethylene-properties-in-the-gas-phase-polymerization-aided-by-neural-network" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/105904.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">144</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">4684</span> Synthesis and Two-Photon Polymerization of a Cytocompatibility Tyramine Functionalized Hyaluronic Acid Hydrogel That Mimics the Chemical, Mechanical, and Structural Characteristics of Spinal Cord Tissue</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=James%20Britton">James Britton</a>, <a href="https://publications.waset.org/abstracts/search?q=Vijaya%20Krishna"> Vijaya Krishna</a>, <a href="https://publications.waset.org/abstracts/search?q=Manus%20Biggs"> Manus Biggs</a>, <a href="https://publications.waset.org/abstracts/search?q=Abhay%20Pandit"> Abhay Pandit</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Regeneration of the spinal cord after injury remains a great challenge due to the complexity of this organ. Inflammation and gliosis at the injury site hinder the outgrowth of axons and hence prevent synaptic reconnection and reinnervation. Hyaluronic acid (HA) is the main component of the spinal cord extracellular matrix and plays a vital role in cell proliferation and axonal guidance. In this study, we have synthesized and characterized a photo-cross-linkable HA-tyramine (tyr) hydrogel from a chemical, mechanical, electrical, biological and structural perspective. From our experimentation, we have found that HA-tyr can be synthesized with controllable degrees of tyramine substitution using click chemistry. The complex modulus (G*) of HA-tyr can be tuned to mimic the mechanical properties of the native spinal cord via optimization of the photo-initiator concentration and UV exposure. We have examined the degree of tyramine-tyramine covalent bonding (polymerization) as a function of UV exposure and photo-initiator use via Photo and Nuclear magnetic resonance spectroscopy. Both swelling and enzymatic degradation assays were conducted to examine the resilience of our 3D printed hydrogel constructs in-vitro. Using a femtosecond 780nm laser, the two-photon polymerization of HA-tyr hydrogel in the presence of riboflavin photoinitiator was optimized. A laser power of 50mW and scan speed of 30,000 μm/s produced high-resolution spatial patterning within the hydrogel with sustained mechanical integrity. Using dorsal root ganglion explants, the cytocompatibility of photo-crosslinked HA-tyr was assessed. Using potentiometry, the electrical conductivity of photo-crosslinked HA-tyr was assessed and compared to that of native spinal cord tissue as a function of frequency. In conclusion, we have developed a biocompatible hydrogel that can be used for photolithographic 3D printing to fabricate tissue engineered constructs for neural tissue regeneration applications. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=3D%20printing" title="3D printing">3D printing</a>, <a href="https://publications.waset.org/abstracts/search?q=hyaluronic%20acid" title=" hyaluronic acid"> hyaluronic acid</a>, <a href="https://publications.waset.org/abstracts/search?q=photolithography" title=" photolithography"> photolithography</a>, <a href="https://publications.waset.org/abstracts/search?q=spinal%20cord%20injury" title=" spinal cord injury"> spinal cord injury</a> </p> <a href="https://publications.waset.org/abstracts/92107/synthesis-and-two-photon-polymerization-of-a-cytocompatibility-tyramine-functionalized-hyaluronic-acid-hydrogel-that-mimics-the-chemical-mechanical-and-structural-characteristics-of-spinal-cord-tissue" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/92107.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">152</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">4683</span> Bulk Amounts of Linear and Cyclic Polypeptides on Our Hand within a Short Time</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Yu%20Zhang">Yu Zhang</a>, <a href="https://publications.waset.org/abstracts/search?q=Il%20Kim"> Il Kim</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Polypeptides with defined peptide sequences illustrate the power of remarkable applications in drug delivery, tissue engineering, sensing and catalysis. Especially the cyclic polypeptides, the distinctive topological architecture imparts many characteristic properties comparing to linear polypeptides. Here, a facile and highly efficient strategy for the synthesis of linear and cyclic polypeptides is reported using N-heterocyclic carbenes (NHCs)-mediated ring-opening polymerization (ROP) of α-amino acid N-carboxyanhydrides (NCA) in the presence or absence of primary amine initiator. The polymerization proceeds rapidly in a quasi-living manner, allowing access to linear and cyclic polypeptides of well-defined chain length and narrow polydispersity, as evidenced by nuclear magnetic resonance spectrum (1H NMR and 13C NMR spectra) and size exclusion chromatography (SEC) analysis. The cyclic architecture of the polypeptides was further verified by matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectra (MALDI-TOF MS) and electrospray ionization (ESI) mass spectra, as well as viscosity studies. This approach can also simplify workup procedures and make bulk scale synthesis possible, which thereby opens avenues for practical uses in diverse areas, opening up the new generation of polypeptide synthesis. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=%CE%B1-amino%20acid%20N-carboxyanhydrides" title="α-amino acid N-carboxyanhydrides">α-amino acid N-carboxyanhydrides</a>, <a href="https://publications.waset.org/abstracts/search?q=living%20polymerization" title=" living polymerization"> living polymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=polypeptides" title=" polypeptides"> polypeptides</a>, <a href="https://publications.waset.org/abstracts/search?q=N-heterocyclic%20carbenes" title=" N-heterocyclic carbenes"> N-heterocyclic carbenes</a>, <a href="https://publications.waset.org/abstracts/search?q=ring-opening%20polymerization" title=" ring-opening polymerization"> ring-opening polymerization</a> </p> <a href="https://publications.waset.org/abstracts/75665/bulk-amounts-of-linear-and-cyclic-polypeptides-on-our-hand-within-a-short-time" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/75665.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">167</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">4682</span> Efficiency of a Molecularly Imprinted Polymer for Selective Removal of Chlorpyrifos from Water Samples</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Oya%20A.%20Urucu">Oya A. Urucu</a>, <a href="https://publications.waset.org/abstracts/search?q=Asl%C4%B1%20B.%20%C3%87i%C4%9Fil"> Aslı B. Çiğil</a>, <a href="https://publications.waset.org/abstracts/search?q=Hatice%20Birtane"> Hatice Birtane</a>, <a href="https://publications.waset.org/abstracts/search?q=Ece%20K.%20Yetimo%C4%9Flu"> Ece K. Yetimoğlu</a>, <a href="https://publications.waset.org/abstracts/search?q=Memet%20Vezir%20Kahraman"> Memet Vezir Kahraman</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Chlorpyrifos is an organophosphorus pesticide which can be found in environmental water samples. The efficiency and reuse of a molecularly imprinted polymer (chlorpyrifos - MIP) were investigated for the selective removal of chlorpyrifos residues. MIP was prepared with UV curing thiol-ene polymerization technology by using multifunctional thiol and ene monomers. The thiol-ene curing reaction is a radical induced process, however unlike other photoinitiated polymerization processes, this polymerization process is a free-radical reaction that proceeds by a step-growth mechanism, involving two main steps; a free-radical addition followed by a chain transfer reaction. It assures a very rapidly formation of a uniform crosslinked network with low shrinkage, reduced oxygen inhibition during curing and excellent adhesion. In this study, thiol-ene based UV-curable polymeric materials were prepared by mixing pentaerythritol tetrakis(3-mercaptopropionate), glyoxal bis diallyl acetal, polyethylene glycol diacrylate (PEGDA) and photoinitiator. Chlorpyrifos was added at a definite ratio to the prepared formulation. Chemical structure and thermal properties were characterized by FTIR and thermogravimetric analysis (TGA), respectively. The pesticide analysis was performed by gas chromatography-mass spectrometry (GC-MS). The influences of some analytical parameters such as pH, sample volume, amounts of analyte concentration were studied for the quantitative recoveries of the analyte. The proposed MIP method was applied to the determination of chlorpyrifos in river and tap water samples. The use of the MIP provided a selective and easy solution for removing chlorpyrifos from the water. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=molecularly%20imprinted%20polymers" title="molecularly imprinted polymers">molecularly imprinted polymers</a>, <a href="https://publications.waset.org/abstracts/search?q=selective%20removal" title=" selective removal"> selective removal</a>, <a href="https://publications.waset.org/abstracts/search?q=thilol-ene" title=" thilol-ene"> thilol-ene</a>, <a href="https://publications.waset.org/abstracts/search?q=uv-curable%20polymer" title=" uv-curable polymer"> uv-curable polymer</a> </p> <a href="https://publications.waset.org/abstracts/44897/efficiency-of-a-molecularly-imprinted-polymer-for-selective-removal-of-chlorpyrifos-from-water-samples" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/44897.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">301</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">4681</span> Conducting Glove Leathers Prepared through in-situ Polymerization of Pyrrole</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Wegene%20Demisie%20Jima">Wegene Demisie Jima</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Leather is a durable and flexible material used for various purposes including clothing, footwear, upholstery and gloves. However, the use of leather for smart product applications is a challenge since it is electrically insulating material. Here, we report a simple method to produce conducting glove leathers using an in-situ polymerization of pyrrole. The concentrations of pyrrole, ferric chloride and anthraquinone-2-sulfonic acid sodium salt monohydrate were optimized to produce maximum conductivity in the treated leathers. The coating of polypyrrole in the treated leathers was probed using FT-IR, X-ray diffraction and electron microscopic analysis. FTIR confirms that the formation of polypyrrole on the leather surface as well as presence of prominent N-C stretching band. X-ray diffraction analysis suggests para-crystallinity in the PPy-treated leathers.We further demonstrate that the treated leathers, with maximum conductivity of 7.4 S/cm, can be used for making conductive gloves for operating touch-screen devices apart from other smart product applications. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=electrical%20conductivity" title="electrical conductivity">electrical conductivity</a>, <a href="https://publications.waset.org/abstracts/search?q=in-situ%20polymerization" title=" in-situ polymerization"> in-situ polymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=pyrrole" title=" pyrrole"> pyrrole</a>, <a href="https://publications.waset.org/abstracts/search?q=smart%20product" title=" smart product"> smart product</a> </p> <a href="https://publications.waset.org/abstracts/84514/conducting-glove-leathers-prepared-through-in-situ-polymerization-of-pyrrole" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/84514.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">193</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=chemical%20polymerization&page=2">2</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=chemical%20polymerization&page=3">3</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=chemical%20polymerization&page=4">4</a></li> <li class="page-item"><a class="page-link" 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