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Dynamic mechanical, rheological, and morphological studies of polyacrylate‐ graft ‐poly (vinyl chloride) suspension resin
Author(s) -
Yuan Jinfeng,
Pan Mingwang,
Wang Xiaomei,
Zhang Liucheng
Publication year - 2007
Publication title -
polymer engineering and science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.503
H-Index - 111
eISSN - 1548-2634
pISSN - 0032-3888
DOI - 10.1002/pen.20750
Subject(s) - materials science , vinyl chloride , glass transition , copolymer , polyvinyl chloride , composite material , dynamic mechanical analysis , rheology , acrylate , suspension polymerization , vinyl ester , toughness , butyl acrylate , polymer chemistry , polymer
A series of polyacrylate‐ graft ‐poly (vinyl chloride) (ACR‐ g ‐PVC) resins were prepared through suspension graft copolymerization. Three kinds of polyacrylate latices were grafted by vinyl chloride using suspension polymerization method at 57 ± 0.1°C, respectively. The dynamic mechanical and rheological properties and the morphology of the resulting ACR‐ g ‐PVC resins were investigated. Poly (butyl acrylate)‐ graft ‐poly (vinyl chloride) (PBA‐ g‐ PVC) resin exhibited better toughness, and the optimized content of PBA in ACR‐ g ‐PVC resin was 6–8 wt%. The melt viscosity of ACR‐ g ‐PVC resin was much lower than that of pure PVC. The nature of the fracture surfaces of ACR‐ g ‐PVC material indicated that it has good toughness. The impact strength of the PBA‐ g ‐PVC material was greatly improved compared with that of pure PVC. The Young's modulus of the ACR‐ g ‐PVC material containing less than 15 wt% of PBA was comparable to that of pure PVC according to their dynamic mechanical analysis curves. For all of the ACR‐ g ‐PVC resins, there were two individual relaxations in the low‐temperature range. One was β transition of PVC, and the other was α transition of ACR. The glass transition temperature of PVC in the ACR‐ g ‐PVC resin shifted to lower temperature when the content of the PBA was above 50 wt%. POLYM. ENG. SCI., 47:996–1003, 2007. © 2007 Society of Plastics Engineers

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