A review on the free radical grafting of vinyl monomers onto polyethylene and polypropylene by reactive extrusion

被引:18
作者
Li, Tian-Tian [1 ]
Cheng, Si-Bo [1 ]
Feng, Lian-Fang [1 ,2 ]
Gu, Xue-Ping [1 ,2 ]
Duan, Jin-Tang [2 ]
Jiang, Ming-Zhe [2 ]
Zhang, Cai-Liang [1 ,2 ]
机构
[1] Zhejiang Univ, Coll Chem & Biol Engn, State Key Lab Chem Engn, Hangzhou 310027, Peoples R China
[2] Inst Zhejiang Univ Quzhou, 78 Jiuhua Blvd North, Quzhou 324000, Peoples R China
基金
中国国家自然科学基金;
关键词
Grafting; Polyolefin; Reactive extrusion; Free radical; Functional monomers; RESIDENCE TIME DISTRIBUTION; IN-SITU COMPATIBILIZATION; POLY(BUTYLENE TEREPHTHALATE) BLENDS; IMMISCIBLE POLYMER BLENDS; MALEIC-ANHYDRIDE; GLYCIDYL METHACRYLATE; ACRYLIC-ACID; ISOTACTIC POLYPROPYLENE; ANIONIC-POLYMERIZATION; MORPHOLOGY DEVELOPMENT;
D O I
10.1016/j.ces.2023.118916
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Polyethylene (PE) and polypropylene (PP) have been widely used in films, pipes, plates, fibers, and electronic devices, etc. due to a good balance between mechanical properties, processability and cost. They are apolar and chemically relatively inert. Sometimes these characteristics may restrain their application. A solution to making them polar and/or chemically reactive is to graft polar and/or functional groups onto their backbones. This can be done by free radical chemistry via a reactive extrusion process which is continuous, solventless and of short residence time (<a few minutes). This review describes problems related to free radical grafting: low grafting yield, monomer residual, and side reactions (especially chain scission for PP and gel formation for PE), and strategies to solve them: addition of comonomers, use of nano-reactors, optimization of screw profile and mixing, sequential feeding of monomers, assistance of supercritical carbon dioxide (scCO2), and devolatilization.
引用
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页数:19
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