氯乙烯/丙烯腈共聚物的合成 氯乙烯/丙烯腈共聚物的合成

氯乙烯/丙烯腈共聚物的合成

  • 期刊名字:合成橡膠工業(yè)
  • 文件大?。?07kb
  • 論文作者:余天石,林嘉平,楊典志,王彤
  • 作者單位:華東理工大學(xué)材料科學(xué)與工程學(xué)院,上海氯堿化工有限公司技術(shù)中心
  • 更新時(shí)間:2020-10-26
  • 下載次數:次
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研究快訊 C合成橡膠工業(yè),2003-07-15,26(4):249CHINA SYNTHETIC RUBBER INDUSTRYSynthesis of vinyl chloride/acrylonitrile copolymerYu Tianshi, Lin Jiaping, Yang Dianzhi, Wang Tong?(I. School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China;2. Technical Center of shanghai Chlor- alkali Chemical Co Ltd, Shanghai 200241, China)63|ADue to the inflammable property and cool like appearance of monomers without the character of the polymerization of the VCthe vinyl chloride(VC)/acrylonitrile(AN)copolymer, it was monomer 2.3widely used in the inflammable textile and artificial fiber. The Table I gives the conversion of the two monomers respecpolymer was usually synthesized by emulsion polymerizationtively. All the data were calculated according to the elementsIn the reaction system, the activities of the two monomers diffnalysis(C, H, N)appreciably with eachTable 1 Conversion of monomersmerization method was adding AN monomer by two steps. That9 Mx 10 Cve/%CAN/%is to say adding part of total AN monomer before the reaction One-step3.05and pumping into the another part during the polymerization In Two-step32.0065this way, the two monomers may copolymerize with each other Step-by-step 43.785.38.166824well to get a proper composition. In the paper, three differentmethods of adding an monomer were compared, one -step,In Table 1, the one -step method got a relatively highertwo-step and step-by-step (according to the adding pro- conversion, both of the total and the monomers, due to fewercess of the AN monomer), to give a comparison and provideN monomer in the system. However, in the other two methsome useful information to the synthesis of this kind copoly- ods, An monomer was continuously added and reacted muchmer. And it was coneluded that the step-by-step method faster than the VC monomer. Therefore, theon of vcprovided a higher conversion of the system than the other two monomer was much lower than the one -step method. As faroccasion. The step-by-step method was not reported so far. as the two-step and the step-by-step methods were con-The polymerization process was followed by tracing the difrmed, the both two methods got polymers with similar relaference of the cooling water temperature( Ti)and the autoclavere molecularhat was much higher than the one-steptemperature( T2). Fig 1 shows the relationship between thethod, and the conversions both of the system and there difference and the reactiomonomers of step-by -step were higher than the two-stepto sAAN monomer was a better method to synthesize the VC/ANcopolymer to get higher conversion both of the system and the0.5monomers. Owing to the higher conversion, the cost of vcAN copolymer can be lowered in step-by -step method whilethe relative molecular mass of the copolymer is similar to thatof the two - step methodJ-one-step; O-two-step: A-step-by-step1Us,US2420330Fig 1 Difference of temperature between cooling water and2 Xie T Y. Joumal of Vinyl Technology, 1991, 13(1): 1-253 Gurkan Karakas. British Polymer Joumal, 1989, 21: 99-406氯乙烯/丙烯膽共聚物的合成余天石,林嘉平As it could be seen, one-step method led the copolymer-楊典志,王彤2(1.華東理工大學(xué)材料科學(xué)與工程學(xué)lacf a to be much more heated than the other two, due to the院,上海20037:2.上海氯堿化工有限公司技術(shù)中心,上of the an monomer after about4h. After reacting4h,海200241)采用3種不同的丙烯腈的加料方式合成了氯almost all an monomer was reacted and the reaction wa乙烯/丙烯腈共聚物,并通過(guò)對冷卻水溫和聚合釜溫度的mainly controlled by the polymerization of the vc monomer監控,描述了反應進(jìn)程。同時(shí),通過(guò)元素分析手段得到了Therefore, VC monomer got more time to re聚合體系和單體的轉化率。通過(guò)研究采用逐步加料方式he other two methods. And the character of the reaction just畫(huà)者相對分子質(zhì)量接like the polymerization of the VC monomer, which haan obvious character of an abrupt increase of the reaction iF中國煤化工:加料方式temperature.And in the other two occasions, the whole reac-CNMHGzation of the twoBiography: Yu Tianshi, Ph D

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