相关链接
联系方式
  • 通信地址:中国湖北省武汉市武昌区友谊大道318号湖北大学材料科学与工程学院
  • 邮编:430062
  • 电话:02788661729
  • 传真:
  • Email:bingbingjiang@gmail.com
当前位置:> 首页 > 论文著作 > 正文
Kinetics of polymerization and particle stabilization mechanism on dispersion copolymerization of styrene and divinylbenzene
作者:H.T. Zhang, J.X. Huang, B.B. Jiang
关键字:polystyrene; radical polymerization; kinetics of copolymerization, particle nucleation, stabilization, dispersion copolymerization
论文来源:期刊
具体来源:J Appl Polym Sci
发表时间:2002年
Monodisperse highly crosslinked microspheres were prepared by dispersion copolymerization of styrene and divinylbenzene in an ethanol/water medium using poly(N-vinylpyrrolidone) (PVP) as the stabilizer. The locus of polymerization and growth of particles were investigated. The polymerization kinetics, average particle diameter (Dn), polydispersity index (PDI), and numbers of particles (Np) were presented. When the initial styrene concentration is below 20%, the results indicate that the polymerization occurs in the particles, and the particles grow to their final size by the diffusion of monomer and oligomer into the existing particles. The polymerization rate can be described by the equation Rp = k[l]0.87 ([St]1.91 + [DVB]0.09) (1 + [PVP]0.01) exp(? 45.35/RT). The data from infrared spectroscopy demonstrated that the graft stabilizer was present. The dissolution experiments show that the crosslinking reaction occurred irregularly in batch dispersion polymerization. Using the postaddition approach, up to 3% divenylbenzene (DVB) was successfully incorporated in the synthesis of coagulum-free substance, and monodisperse crosslinked 5 μ m microspheres with a superior resistance to solvents have been prepared.