详细信息
Crystallization Kinetics of Isotactic Polypropylene Nucleated with Organic Dicarboxylic Acid Salts ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:Crystallization Kinetics of Isotactic Polypropylene Nucleated with Organic Dicarboxylic Acid Salts
作者:Zhao, Shicheng[1];Xin, Zhong[1]
机构:[1]E China Univ Sci & Technol, Dept Sch Chem Engn, State Key Lab Chem Engn & Prod Engn, Shanghai 200237, Peoples R China
年份:2009
卷号:112
期号:3
起止页码:1471
外文期刊名:JOURNAL OF APPLIED POLYMER SCIENCE
收录:;EI(收录号:20091712043588);WOS:【SCI-EXPANDED(收录号:WOS:000264247300044)】;
基金:Contract grant sponsor: National Natural Science Foundation of China; contract grant number: 20876042.
语种:英文
外文关键词:crystallization kinetics; nucleating agent; isotactic polypropylene; bicyclo[2.2.1]heptene dicarboxylate salts
摘要:Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate salts (BCHED) were synthesized by hydrothermal method. The crystallization kinetics of isotactic polypropylene (iPP) and nucleated iPP with BCHED were investigated by differential scanning calorimeter (DSC) under isothermal and nonisothermal conditions. Isothermal crystallization kinetics was described by Avrami equation and the fold surface free energy (sigma(e)) of iPP was calculated by Hoffman theory. The results showed Avrami exponents of nucleated iPP become smaller, the values of t(1/2) dramatically decrease, the crystallization rate constants Z(T) greatly increase and the fold surface free energy (sigma(e)) of iPP decrease with the addition of the nucleating agents. Under nonisothermal condition the Caze method was applied to deal with the crystallization kinetics of iPP and the crystallization active energy of iPP was determined by Kissinger method. The results showed the crystallization peak temperatures (T-cp) of nucleated iPP greatly increase, but Avrami exponents of iPP were slightly influenced and the crystallization active energy of iPP increases by the addition of BCHED. It can be concluded that BCHED act as nucleating agents and BCHE11 shows the best nucleating effect. (C) 2009 Wiley Periodicals, Inc. J Appl Polym Sci 112: 1471-1480, 2009
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