Hypercrosslinked Polystyrene Microspheres with Bimodal Pore Size Distribution and Controllable Macroporosity

被引:4
作者
Liu, Qingquan [1 ,2 ]
Wang, Li [1 ]
Yu, Weiting [1 ]
Xiao, Anguo [1 ]
Yu, Haojie [1 ]
Huo, Jia [1 ]
机构
[1] Zhejiang Univ, State Key Lab Chem Engn, Coll Mat Sci & Chem Engn, Hangzhou 310027, Peoples R China
[2] Hunan Univ Sci & Technol, Coll Chem & Chem Engn, Xiangtan 411201, Peoples R China
关键词
crosslinking; polystyrene; macroporous polymers; CROSS-LINKED POLYSTYRENE; NETWORKS; CATALYST; POROSITY; RESINS;
D O I
10.1002/app.31422
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A combination Of Suspension polymerization and postcrosslinking was used to prepare hypercrosslinked polystyrene (H-PS) microspheres with controllably bimodal pc re size distribution in the presence of toluene and polypropylene (PP) as a coporogen. The proportion of PP in the coporogen was changed to investigate the influence of the coporogen composition on the pore structure of the H-PS microspheres. The addition of a small amount of PP achieved the aim of a clearly bimodal pore size distribution and the control of the macroporosity of the H-PS microspheres, which have potential application in the preparation of catalyst Supports. The specific surface area of the H-PS microspheres could be adjusted in the range 380-790 m(2)/g by changes in the concentration of FT in the coporogen. Moreover, the H-PS microspheres displayed all the characteristics of Davankov-type resins by their ability to be swollen in both thermodynamically poor solvents such as water and good solvents such as toluene. Finally, the possible mechanism of porosity formation during polymerization and postcrosslinking was also examined by a combination of pore structure data and the appearance of the microspheres before and after postcrosslinking. (C) 2009 Wiley Periodicals, Inc. J Appl Polym Sci 116: 84-92, 2010
引用
收藏
页码:84 / 92
页数:9
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