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Effect of copolymer composition on the miscibility of blends of styrene-acrylonitrile copolymers with poly (methyl methacrylate)
Affiliation:1. College of Instrumentation and Electrical Engineering, Jilin University, Changchun 130000, China;2. Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences, No. 266 Fangzheng Avenue, Shuitu Hi-Tech Park, Shuitu Town, Beibei District, Chongqing 400714, China;3. Chongqing Academy of Metrology and Quality Inspection, Chongqing 401123, China;1. Department of Surgery, Yonsei University College of Medicine Pancreaticobiliary Cancer Clinic, Institute of Gastroenterology, Severance Hospital, Seoul, Republic of Korea;2. Department of Radiology, Yonsei University College of Medicine Pancreaticobiliary Cancer Clinic, Institute of Gastroenterology, Severance Hospital, Seoul, Republic of Korea;3. Department of Pathology, Yonsei University College of Medicine Pancreaticobiliary Cancer Clinic, Institute of Gastroenterology, Severance Hospital, Seoul, Republic of Korea;4. Department of Surgery, Bundang CHA Hospital, CHA University College of Medicine, Seongnam, Republic of Korea
Abstract:The phase behaviour for blends of various polymethacrylates with styrene-acrylonitrile (SAN) copolymers has been examined as a function of the acrylonitrile content of the copolymer. Poly(methyl methacrylate), poly(ethyl methacrylate) and poly(n-propyl methacrylate) were found to be miscible with SANs over a limited window of acrylonitrile contents while no SANs appear to be miscible with poly(isopropyl methacrylate) or poly(n-butyl methacrylate). These conclusions were reached on the basis of lower critical solution temperature (LCST) and glass transition temperature behaviour. All miscible blends exhibited phase separation on heating, LCST behaviour, at temperatures which varied greatly with copolymer composition. An optimum acrylonitrile (AN) level ranging from about 10 to 14% by weight resulted in the highest temperatures for phase separation which has important implications for selection of SANs to produce homogeneous mixtures by melt processing. The basis for miscibility in these systems is evidently repulsion between styrene and acrylonitrile units in the copolymer as explained by recent models. The excess volumes for all blends are zero within experimental accuracy which suggests that the interactions for miscibility are relatively weak even for the optimum AN level. This interaction becomes smaller the larger or more bulky is the alkyl side group of the polymethacrylate.
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