Improvement of Poly(ethylene terephthalate) Melt-Foamability by Long-Chain Branching with the Combination of Pyromellitic Dianhydride and Triglycidyl Isocyanurate

被引:61
作者
Ge, Yukai [1 ]
Yao, Shun [1 ]
Xu, Menlong [1 ]
Gao, Liang [1 ]
Fang, Zhiying [1 ]
Zhao, Ling [1 ,2 ]
Liu, Tao [1 ]
机构
[1] East China Univ Sci & Technol, Shanghai Key Lab Multiphase Mat Chem Engn, Shanghai 200237, Peoples R China
[2] XinJiang Univ, Sch Chem & Chem Engn, Urumqi 830046, Peoples R China
关键词
LOW-DENSITY POLYETHYLENE; MOLECULAR-WEIGHT DISTRIBUTION; RELAXATION-TIME SPECTRA; ELONGATIONAL VISCOSITY; RHEOLOGICAL PROPERTIES; RECYCLED PET; STRENGTH; EXTRUSION; POLYPROPYLENE; EXTENSION;
D O I
10.1021/acs.iecr.8b04157
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Reactive processing on conventional poly(ethylene terephthalate) (PET) with the combination of pyromellitic dianhydride (PMDA) and triglycidyl isocyanurate (TGIC) was used to produce long-chain branched PET (LCB-PET). The branching factors of the PET samples were correlated from their intrinsic viscosity and molar mass results. In all PET samples without a cross-linked structure, PET modified with 0.1 wt % PMDA and 0.5 wt % TGIC (PET-P1T5) had the highest branching degree, with a branching factor of 0.84. The relaxation time spectra of the three modified PET samples with strain-hardening behaviors displayed rubbery states during the relaxation process, which was ascribed to their increased molecular weight or long-chain branched structure. Batch melt-foaming experiments with CO2 were carried out to evaluate the melt-foamability of PET. The results indicated that both a high molecular weight and long-chain branched structure, especially the latter, could efficiently lead to strong molecular entanglements and significantly improve the polymer melt-foamability.
引用
收藏
页码:3666 / 3678
页数:13
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