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polymerization</title> <meta name="description" content="Search results for: degree of polymerization"> <meta name="keywords" content="degree of 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 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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="degree of 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> 3020</div> </div> </div> </div> <h1 class="mt-3 mb-3 text-center" style="font-size:1.6rem;">Search results for: degree of polymerization</h1> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">3020</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">3019</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">3018</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">3017</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">3016</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">3015</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">3014</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">3013</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">3012</span> Biostimulant Activity of Chitooligomers: Effect of Different Degrees of Acetylation and Polymerization on Wheat Seedlings under Salt Stress</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Xiaoqian%20Zhang">Xiaoqian Zhang</a>, <a href="https://publications.waset.org/abstracts/search?q=Ping%20Zou"> Ping Zou</a>, <a href="https://publications.waset.org/abstracts/search?q=Pengcheng%20Li"> Pengcheng Li</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Salt stress is one of the most serious abiotic stresses, and it can lead to the reduction of agricultural productivity. High salt concentration makes it more difficult for roots to absorb water and disturbs the homeostasis of cellular ions resulting in osmotic stress, ion toxicity and generation of reactive oxygen species (ROS). Compared with the normal physiological conditions, salt stress could inhibit the photosynthesis, break metabolic balance and damage cellular structures, and ultimately results in the reduction of crop yield. Therefore it is vital to develop practical methods for improving the salt tolerance of plants. Chitooligomers (COS) is partially depolymerized products of chitosan, which is consisted of D-glucosamine and N-acetyl-D-glucosamine. In agriculture, COS has the ability to promote plant growth and induce plant innate immunity. The bioactivity of COS closely related to its degree of polymerization (DP) and acetylation (DA). However, most of the previous reports fail to mention the function of COS with different DP and DAs in improving the capacity of plants against salt stress. Accordingly, in this study, chitooligomers (COS) with different degrees of DAs were used to test wheat seedlings response to salt stress. In addition, the determined degrees of polymerization (DPs) COS(DP 4-12) and a heterogeneous COS mixture were applied to explore the relationship between the DP of COSs and its effect on the growth of wheat seedlings in response to salt stress. It showed that COSs, the exogenous elicitor, could promote the growth of wheat seedling, reduce the malondialdehyde (MDA) concentration, and increase the activities of antioxidant enzymes. The results of mRNA expression level test for salt stress-responsive genes indicated that COS keep plants away from being hurt by the salt stress via the regulation of the concentration and the increased antioxidant enzymes activities. Moreover, it was found that the activities of COS was closely related to its Das and COS (DA: 50%) displayed the best salt resistance activity to wheat seedlings. The results also showed that COS with different DP could promote the growth of wheat seedlings under salt stress. COS with a DP (6-8) showed better activities than the other tested samples, implied its activity had a close relationship with its DP. After treatment with chitohexaose, chitoheptaose, and chitooctaose, the photosynthetic parameters were improved obviously. The soluble sugar and proline contents were improved by 26.7%-53.3% and 43.6.0%-70.2%, respectively, while the concentration of malondialdehyde (MDA) was reduced by 36.8% - 49.6%. In addition, the antioxidant enzymes activities were clearly activated. At the molecular level, the results revealed that they could obviously induce the expression of Na+/H+ antiporter genes. In general, these results were fundamental to the study of action mechanism of COS on promoting plant growth under salt stress and the preparation of plant growth regulator. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=chitooligomers%20%28COS%29" title="chitooligomers (COS)">chitooligomers (COS)</a>, <a href="https://publications.waset.org/abstracts/search?q=degree%20of%20polymerization%20%28DP%29" title=" degree of polymerization (DP)"> degree of polymerization (DP)</a>, <a href="https://publications.waset.org/abstracts/search?q=degree%20of%20acetylation%20%28DA%29" title=" degree of acetylation (DA)"> degree of acetylation (DA)</a>, <a href="https://publications.waset.org/abstracts/search?q=salt%20stress" title=" salt stress"> salt stress</a> </p> <a href="https://publications.waset.org/abstracts/80333/biostimulant-activity-of-chitooligomers-effect-of-different-degrees-of-acetylation-and-polymerization-on-wheat-seedlings-under-salt-stress" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/80333.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">175</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">3011</span> Weighted G2 Multi-Degree Reduction of Bezier Curves</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Salisu%20ibrahim">Salisu ibrahim</a>, <a href="https://publications.waset.org/abstracts/search?q=Abdalla%20Rababah"> Abdalla Rababah</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this research, we use Weighted G2-Multi-degree reduction of Bezier curve of degree n to a Bezier curve of degree m, m < n. The degree reduction of Bezier curves is used to represent a given Bezier curve of n by a Bezier curve of degree m, m < n. Exact degree reduction is not possible, and degree reduction is approximate process in nature. We derive a weighted degree reducing method that is geometrically continuous at the end points. Different norms will be considered, several error minimizations will be given. The proposed methods produce error function that are less than the errors of existing methods. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Bezier%20curves" title="Bezier curves">Bezier curves</a>, <a href="https://publications.waset.org/abstracts/search?q=multiple%20degree%20reduction" title=" multiple degree reduction"> multiple degree reduction</a>, <a href="https://publications.waset.org/abstracts/search?q=geometric%20continuity" title=" geometric continuity"> geometric continuity</a>, <a href="https://publications.waset.org/abstracts/search?q=error%20function" title=" error function"> error function</a> </p> <a href="https://publications.waset.org/abstracts/18669/weighted-g2-multi-degree-reduction-of-bezier-curves" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/18669.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">481</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">3010</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">3009</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">3008</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">3007</span> Symmetric Polymerization with Dynamical Resolution</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Muddser%20Ghaffar">Muddser Ghaffar</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In material science, synthetic chiral polymers are becoming increasingly significant due to their distinct properties that distinguish them from other polymer materials. One special technique for producing well-defined chiral polymers is asymmetric kinetic resolution polymerization (AKRP), which adds stereo regularity to a polymer chain by the kinetic resolution of a race mate preferentially polymerizing one enantiomer. Apart from making it possible to characterize chiral polymers enantioselective, AKRP can synthesize chiral polymers with high stereo selectivity. This review includes the literature on the use of enzymes, chiral metal complexes, and organ catalysts as AKRP promoters. One enantiomer reacts more quickly than the other in this kind of polymerisation, quickly entering the expanding polymer chain, while the kinetically less reactive enantiomer stays unreactive and is readily separated using straightforward purification techniques. The degree of chiral induction and overall chirality of the chiral polymers that are generated may be assessed using the enantiomeric excess (ee) of the initial monomer, which is frequently determined by chiral HPLC analysis, throughout the polymerisation process. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=stereo%20regularity" title="stereo regularity">stereo regularity</a>, <a href="https://publications.waset.org/abstracts/search?q=polymers" title=" polymers"> polymers</a>, <a href="https://publications.waset.org/abstracts/search?q=dynamical" title=" dynamical"> dynamical</a>, <a href="https://publications.waset.org/abstracts/search?q=symmetric" title=" symmetric"> symmetric</a> </p> <a href="https://publications.waset.org/abstracts/193168/symmetric-polymerization-with-dynamical-resolution" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/193168.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">13</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">3006</span> Comparison of Depth of Cure and Degree of Conversion between Opus Bulk Fill and X-Tra Fill Bulk Fill Composites</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Yasaman%20Samani">Yasaman Samani</a>, <a href="https://publications.waset.org/abstracts/search?q=Ali%20Golmohammadi"> Ali Golmohammadi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Introduction: The degree of conversion and depth of cure affects the clinical success of resin composite restorations directly. One of the main challenges in achieving a successful composite restoration is the achievement of sufficient depth of cure. The insufficient polymerization may lead to a decrease in the physical/mechanical and biological properties of resin composites and, as a result of that, unsuccessful composite restoration. Thus, because of the importance of studying and evaluating the depth of cure and degree of conversion in bulk-fill composites, we decided to evaluate and compare the degree of conversion and depth of cure in two bulk-fill composites; x-tra fill (Voco, Germany) and Opus Bulk fill APS (FGM, Brazil). Materials and Methods: Composite resin specimens (n=10) per group were prepared as cylinder blocks (4×8 mm) with bulk-fill composites, x-tra fil (Voco, Germany) designated as Group A, and Opus Bulk fill APS (FGM, Brazil) designated as Group B. Depth of cure was determined according to “ISO 4049; Depth of Cure” method, In which each specimen were cured (iLED, Woodpecker, China) 40 seconds and FTIR spectroscopy method was used to estimate the degree of conversion of both the bulk-fill composites. The degree of conversion of monomer to polymer was estimated individually in the coronal half (Group A1 and B1) and pulpal half (Group A2 and Group B2) by dividing each specimen into two halves. The data were analyzed using a Student’s t-test and one-way ANOVA at a 5% level of significance. Results: The mean depth of cure in x-tra fil (Voco, Germany) was 3.99 (±0.16), and for Opus Bulk fill, APS (FGM, Brazil) was 2.14 (±0.3). The degree of conversion percentage in Group A1 was 82.7 (±6.1), in group A2 was 73.4 (±5.2), in group B1 was 63.3 (±4.7) and in Group B2 was 56.5 (±7.7). Statistical analysis revealed a significant difference in the depth of cure between the two bulk-fill composites with x-tra fil (Voco, Germany) higher than Opus Bulk fill APS (FGM, Brazil) (P<0.001). The degree of conversion percentage also showed a significant difference, Group A1 being higher than A2 (P=0.0085), B1, and B2 (P<0.001). Group A2 was also higher than B1 (P=0.003) and B2 (P<0.001). There was no significant difference between B1 and B2 (P=0.072). Conclusion: The results indicate that x-tra fill has more depth of cure and a higher percentage of the degree of conversion than Opus Bulk fill APS. The coronal half of x-tra fil had the highest depth of cure percentage (82.66%), and the pulpal half of Opus Bulk fill APS had the lowest percentage (56.45%). Even though both bulk-fill composite materials had an acceptable degree of conversion (55% and higher), x-tra fill has shown better results. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=depth%20of%20cure" title="depth of cure">depth of cure</a>, <a href="https://publications.waset.org/abstracts/search?q=degree%20of%20conversion" title=" degree of conversion"> degree of conversion</a>, <a href="https://publications.waset.org/abstracts/search?q=bulk-fill%20composite" title=" bulk-fill composite"> bulk-fill composite</a>, <a href="https://publications.waset.org/abstracts/search?q=FTIR" title=" FTIR"> FTIR</a> </p> <a href="https://publications.waset.org/abstracts/151692/comparison-of-depth-of-cure-and-degree-of-conversion-between-opus-bulk-fill-and-x-tra-fill-bulk-fill-composites" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/151692.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">102</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">3005</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">3004</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">3003</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">3002</span> Correlation Volumic Shrinkage, Conversion Degree of Dental Composites</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=A.%20Amirouche">A. Amirouche</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Mouzali"> M. Mouzali</a>, <a href="https://publications.waset.org/abstracts/search?q=D.%20C.%20Watts"> D. C. Watts </a> </p> <p class="card-text"><strong>Abstract:</strong></p> During polymerization of dental composites, the volumic shrinkage is related to the conversion degree. The variation of the volumic shrinkage (S max according to the degree of conversion CD.), was examined for the experimental composites: (BisGMA/TEGDMA): (50/50), (75/25), (25/75) mixed with seven radiopac fillers: La2O3, BaO, BaSO4, SrO, ZrO2 , SrZrO3 and BaZrO 3 with different contents in weight, from 0 to 80%. We notice that whatever the filler and the composition in monomers, Smax increases with the increase in CD. This variation is, linear in particular in the case of the fillers containing only one heavy metal, and that whatever the composition in monomers. For a given salt, the increase of BisGMA composition leads to significant increase of S max more pronounced than the increase in CD. The variation of ratio (S max / CD.) with the increase of filler content is negligible. However the fillers containing two types of heavy metals have more effect on the volumic shrinkage than on the degree of conversion. Whatever the composition in monomer, and the content of filler containing only one heavy atom, S max increases with the increase in CD. Nevertheless, S max is affected by the viscosity of the medium compared with CD. For high percentages of mineral fillers (≥ 70% in weight), the diagrams S max according to CD are deviated of the linearity, owing to the fact that S max is affected by the high percentage of fillers compared with CD. The number of heavy atoms influences directly correlation (S max / CD.). In the case of the two mineral fillers: SrZrO3 and BaZrO3 ratio (S max / CD) moves away from the proportionality. The linearity of the diagrams Smax according to CD is less regular, due to the viscosity of high content of BisGMA. The study of Smax and DC of four commercial composites are presented and compared to elaborate experimental composites. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Dental%20composites" title="Dental composites">Dental composites</a>, <a href="https://publications.waset.org/abstracts/search?q=degree%20of%20conversion" title=" degree of conversion"> degree of conversion</a>, <a href="https://publications.waset.org/abstracts/search?q=volumic%20shrinkage" title=" volumic shrinkage"> volumic shrinkage</a>, <a href="https://publications.waset.org/abstracts/search?q=photopolymerization" title=" photopolymerization "> photopolymerization </a> </p> <a href="https://publications.waset.org/abstracts/19487/correlation-volumic-shrinkage-conversion-degree-of-dental-composites" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/19487.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">373</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">3001</span> Target Drug Delivery of Pamidronate Nanoparticles for Enhancing Osteoblastic Activity in Osteoporosis</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Purnima%20Rawat">Purnima Rawat</a>, <a href="https://publications.waset.org/abstracts/search?q=Divya%20Vohora"> Divya Vohora</a>, <a href="https://publications.waset.org/abstracts/search?q=Sarika%20Gupta"> Sarika Gupta</a>, <a href="https://publications.waset.org/abstracts/search?q=Farhan%20J.%20Ahmad"> Farhan J. Ahmad</a>, <a href="https://publications.waset.org/abstracts/search?q=Sushama%20Talegaonkar"> Sushama Talegaonkar </a> </p> <p class="card-text"><strong>Abstract:</strong></p> Nanoparticles (NPs) that target bone tissue were developed using PLGA–mPEG (poly(lactic-co-glycolic-acid)–polyethylene glycol) diblock copolymers by using pamidronate as a bone-targeting moieties. These NPs are expected to enable the transport of hydrophilic drugs. The NP was prepared by in situ polymerization method, and their in- vitro characteristics were evaluated using dynamic light scattering, transmission electron microscopy (TEM) and in phosphate-buffered solution. The bone targeting potential of the NP was also evaluated on in-vitro pre-osteoblast MCT3E1 cell line using ALP activity, degree of mineralization and RT-PCR assay. The average particle size of the NP was 101.6 ± 3.7nm, zeta potential values were negative (-25±0.34mV) of the formulations and the entrapment efficiency was 93± 3.1 % obtained. The moiety of the PLGA–mPEG–pamidronate NPs exhibited the best apatite mineral binding ability in-vitro MCT3E1 pre-osteoblast cell line. Our results suggested that the developed nanoparticles may use as a delivery system for Pamidronate in bone repair and regeneration, warranting further evaluation of the treatment of bone disease. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=nanoparticle" title="nanoparticle">nanoparticle</a>, <a href="https://publications.waset.org/abstracts/search?q=pamidronate" title=" pamidronate"> pamidronate</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=osteoblast" title=" osteoblast"> osteoblast</a> </p> <a href="https://publications.waset.org/abstracts/25173/target-drug-delivery-of-pamidronate-nanoparticles-for-enhancing-osteoblastic-activity-in-osteoporosis" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/25173.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">482</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">3000</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">2999</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">2998</span> On the Zeros of the Degree Polynomial of a Graph</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=S.%20R.%20Nayaka">S. R. Nayaka</a>, <a href="https://publications.waset.org/abstracts/search?q=Putta%20Swamy"> Putta Swamy</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Graph polynomial is one of the algebraic representations of the Graph. The degree polynomial is one of the simple algebraic representations of graphs. The degree polynomial of a graph G of order n is the polynomial Deg(G, x) with the coefficients deg(G,i) where deg(G,i) denotes the number of vertices of degree i in G. In this article, we investigate the behavior of the roots of some families of Graphs in the complex field. We investigate for the graphs having only integral roots. Further, we characterize the graphs having single roots or having real roots and behavior of the polynomial at the particular value is also obtained. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=degree%20polynomial" title="degree polynomial">degree polynomial</a>, <a href="https://publications.waset.org/abstracts/search?q=regular%20graph" title=" regular graph"> regular graph</a>, <a href="https://publications.waset.org/abstracts/search?q=minimum%20and%20maximum%20degree" title=" minimum and maximum degree"> minimum and maximum degree</a>, <a href="https://publications.waset.org/abstracts/search?q=graph%20operations" title=" graph operations"> graph operations</a> </p> <a href="https://publications.waset.org/abstracts/56602/on-the-zeros-of-the-degree-polynomial-of-a-graph" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/56602.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">249</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">2997</span> The Vertex Degree Distance of One Vertex Union of the Cycle and the Star</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ying%20Wang">Ying Wang</a>, <a href="https://publications.waset.org/abstracts/search?q=Haiyan%20Xie"> Haiyan Xie</a>, <a href="https://publications.waset.org/abstracts/search?q=Aoming%20Zhang"> Aoming Zhang</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The degree distance of a graph is a graph invariant that is more sensitive than the Wiener index. In this paper, we calculate the vertex degree distances of one vertex union of the cycle and the star, and the degree distance of one vertex union of the cycle and the star. These results lay a foundation for further study on the extreme value of the vertex degree distances, and the distribution of the vertices with the extreme value in one vertex union of the cycle and the star. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=degree%20distance" title="degree distance">degree distance</a>, <a href="https://publications.waset.org/abstracts/search?q=vertex-degree-distance" title=" vertex-degree-distance"> vertex-degree-distance</a>, <a href="https://publications.waset.org/abstracts/search?q=one%20vertex%20union%20of%20a%20cycle%20and%20a%20star" title=" one vertex union of a cycle and a star"> one vertex union of a cycle and a star</a>, <a href="https://publications.waset.org/abstracts/search?q=graph" title=" graph"> graph</a> </p> <a href="https://publications.waset.org/abstracts/127232/the-vertex-degree-distance-of-one-vertex-union-of-the-cycle-and-the-star" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/127232.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">154</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">2996</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> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2995</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">2994</span> Additive Manufacturing of Microstructured Optical Waveguides Using Two-Photon Polymerization</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Leonnel%20Mhuka">Leonnel Mhuka</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Background: The field of photonics has witnessed substantial growth, with an increasing demand for miniaturized and high-performance optical components. Microstructured optical waveguides have gained significant attention due to their ability to confine and manipulate light at the subwavelength scale. Conventional fabrication methods, however, face limitations in achieving intricate and customizable waveguide structures. Two-photon polymerization (TPP) emerges as a promising additive manufacturing technique, enabling the fabrication of complex 3D microstructures with submicron resolution. Objectives: This experiment aimed to utilize two-photon polymerization to fabricate microstructured optical waveguides with precise control over geometry and dimensions. The objective was to demonstrate the feasibility of TPP as an additive manufacturing method for producing functional waveguide devices with enhanced performance. Methods: A femtosecond laser system operating at a wavelength of 800 nm was employed for two-photon polymerization. A custom-designed CAD model of the microstructured waveguide was converted into G-code, which guided the laser focus through a photosensitive polymer material. The waveguide structures were fabricated using a layer-by-layer approach, with each layer formed by localized polymerization induced by non-linear absorption of the laser light. Characterization of the fabricated waveguides included optical microscopy, scanning electron microscopy, and optical transmission measurements. The optical properties, such as mode confinement and propagation losses, were evaluated to assess the performance of the additive manufactured waveguides. Conclusion: The experiment successfully demonstrated the additive manufacturing of microstructured optical waveguides using two-photon polymerization. Optical microscopy and scanning electron microscopy revealed the intricate 3D structures with submicron resolution. The measured optical transmission indicated efficient light propagation through the fabricated waveguides. The waveguides exhibited well-defined mode confinement and relatively low propagation losses, showcasing the potential of TPP-based additive manufacturing for photonics applications. The experiment highlighted the advantages of TPP in achieving high-resolution, customized, and functional microstructured optical waveguides. Conclusion: his experiment substantiates the viability of two-photon polymerization as an innovative additive manufacturing technique for producing complex microstructured optical waveguides. The successful fabrication and characterization of these waveguides open doors to further advancements in the field of photonics, enabling the development of high-performance integrated optical devices for various applications <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Additive%20Manufacturing" title="Additive Manufacturing">Additive Manufacturing</a>, <a href="https://publications.waset.org/abstracts/search?q=Microstructured%20Optical%20Waveguides" title=" Microstructured Optical Waveguides"> Microstructured Optical Waveguides</a>, <a href="https://publications.waset.org/abstracts/search?q=Two-Photon%20Polymerization" title=" Two-Photon Polymerization"> Two-Photon Polymerization</a>, <a href="https://publications.waset.org/abstracts/search?q=Photonics%20Applications" title=" Photonics Applications"> Photonics Applications</a> </p> <a href="https://publications.waset.org/abstracts/171074/additive-manufacturing-of-microstructured-optical-waveguides-using-two-photon-polymerization" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/171074.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">100</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2993</span> Synthesis of α-Diimin Nickel(II) Catalyst Supported on Graphene and Graphene Oxide for Ethylene Slurry Polymerization</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mehrji%20Khosravan">Mehrji Khosravan</a>, <a href="https://publications.waset.org/abstracts/search?q=Mostafa%20Fathali-Sianib"> Mostafa Fathali-Sianib</a>, <a href="https://publications.waset.org/abstracts/search?q=Davood%20Soudbar"> Davood Soudbar</a>, <a href="https://publications.waset.org/abstracts/search?q=Sasan%20Talebnezhad"> Sasan Talebnezhad</a>, <a href="https://publications.waset.org/abstracts/search?q=Mohammad-Reza%20Ebrahimi"> Mohammad-Reza Ebrahimi </a> </p> <p class="card-text"><strong>Abstract:</strong></p> The late transition metal catalyst of the end group of transition metals in the periodic table as Ni, Fe, Co, and Pd was grown up rapidly in polyolefin industries recently. These metals with suitable ligands exhibited special characteristic properties and appropriate activities in the production of polyolefins. The ligand 1,4-bis (2,6-diisopropyl phenyl) acenaphthene was synthesized by reaction of 2,6-diisopropyl aniline and acenaphthenequinone. The ligand was added to nickel (II) dibromide salt for synthesis the 1,4-bis (2,6 diisopropylphenyl) acenaphthene nickel (II) dibromide catalyst. The structure of the ligand characterized by IR technique. The catalyst then deposited on graphene and graphene oxide by vander walss-attachment for use in Ethylene slurry polymerization process in the presence of catalyst activator such as methylaluminoxane (MAO) in hexane solvent. The structure of the catalyst characterized by IR and TEM techniques and some of the polymers were characterized by DSC. The highest activity was achieved at 600 C for catalyst. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=%CE%B1-diimine%20nickel%20%28II%29%20complex" title="α-diimine nickel (II) complex">α-diimine nickel (II) complex</a>, <a href="https://publications.waset.org/abstracts/search?q=graphene%20as%20supported%20catalyst" title=" graphene as supported catalyst"> graphene as supported catalyst</a>, <a href="https://publications.waset.org/abstracts/search?q=late%20transition%20metal" title=" late transition metal"> late transition metal</a>, <a href="https://publications.waset.org/abstracts/search?q=ethylene%20polymerization" title=" ethylene polymerization"> ethylene polymerization</a> </p> <a href="https://publications.waset.org/abstracts/22317/synthesis-of-a-diimin-nickelii-catalyst-supported-on-graphene-and-graphene-oxide-for-ethylene-slurry-polymerization" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/22317.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">386</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">2992</span> Research on the Effect of Coal Ash Slag Structure Evolution on Its Flow Behavior During Co-gasification of Coal and Indirect Coal Liquefaction Residue</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Linmin%20Zhang">Linmin Zhang</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Entrained-flow gasification technology is considered the most promising gasification technology because of its clean and efficient utilization characteristics. The stable fluidity of slag at high temperatures is the key to affecting the long-period operation of the gasifier. The diversity and differences of coal ash-slag systems make it difficult to meet the requirements for stable slagging in entrained-flow gasifiers. Therefore, coal blending or adding fluxes has been used in industry for a long time to improve the flow behavior of coal ash. As a by-product of the indirect coal liquefaction process, indirect coal liquefaction residue (ICLR) is a kind of industrial solid waste that is usually disposed of by stacking or landfilling. However, this disposal method will not only occupy land resources but also cause serious pollution to soil and water bodies by leachate containing toxic and harmful metals. As a carbon-containing matrix, ICLR is not only a kind of waste but also a kind of energy substance. Utilizing existing industrial gasifiers to blend combustion ICLR can not only transform industrial solid waste into fuel but also save coal resources. Moreover, the ICLR usually contains a unique ash chemical composition different from coal, which will affect the slagging performance of the gasifier. Therefore, exploring the effect of the ash addition in ICLR on the coal ash flow behavior can not only improve the slagging performance and gasification efficiency of entrained-flow gasifier by using the unique ash chemical composition of ICLR but also provide some theoretical support for the large-scale consumption of industrial solid waste. Combining molecular dynamics simulation with Raman spectroscopy experiment, the effect of ICLR addition on slag structure and fluidity was explained, and the relationship between the evolution law of slag short/medium range microstructure and macroscopic flow behavior was discussed. The research found that the high silicon and aluminum content in coal ash led to the formation of complex [SiO₄]⁴- tetrahedron and [AlO₄]⁵- tetrahedron structures at high temperature, and the [SiO₄]⁴- tetrahedron and [AlO₄]⁵- tetrahedron were connected by oxygen atoms to form a multi-membered ring structure with high polymerization degree. Due to the action of the multi-membered ring structure, the internal friction in the slag increased, and the viscosity value was higher on the macro-level. As a network-modified ion, Fe2+ could replace Si4+ and Al3+ in the multi-membered ring structure and combine with O2-, which will destroy the bridge oxygen (BO) structure and transform more complex tri cluster oxygen (TO) and bridge oxygen (BO) into simple non-bridge oxygen (NBO) structure. As a result, a large number of multi-membered rings with high polymerization degrees were depolymerized into low-membered rings with low polymerization degrees. The evolution of oxygen types and ring structures in slag reduced the structure complexity and polymerization degree of coal ash slag, resulting in a decrease in the viscosity of coal ash slag. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=ash%20slag" title="ash slag">ash slag</a>, <a href="https://publications.waset.org/abstracts/search?q=coal%20gasification" title=" coal gasification"> coal gasification</a>, <a href="https://publications.waset.org/abstracts/search?q=fluidity" title=" fluidity"> fluidity</a>, <a href="https://publications.waset.org/abstracts/search?q=industrial%20solid%20waste" title=" industrial solid waste"> industrial solid waste</a>, <a href="https://publications.waset.org/abstracts/search?q=slag%20structure" title=" slag structure"> slag structure</a> </p> <a href="https://publications.waset.org/abstracts/188892/research-on-the-effect-of-coal-ash-slag-structure-evolution-on-its-flow-behavior-during-co-gasification-of-coal-and-indirect-coal-liquefaction-residue" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/188892.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">29</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">2991</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> <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=degree%20of%20polymerization&page=2">2</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=degree%20of%20polymerization&page=3">3</a></li> <li class="page-item"><a class="page-link" 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