聚合
高分子化学
沉淀聚合
化学工程
基质(水族馆)
单体
材料科学
链生长聚合
丙烯酸
聚苯乙烯
自由基聚合
化学
聚合物
复合材料
工程类
地质学
海洋学
作者
Akishige Kii,Jian Xu,Jian Ping Gong,Yoshihito Osada,Xianmin Zhang
摘要
The substrate effect on the inhomogeneous gelation is in situ studied using various monomers: 2-acrylamide-2-methyl-1-propanesulfonic acid (AMPS), acrylic acid, and N,N'-dimethylacrylamide on various hydrophobic substrates with different surface tensions: poly(tetrafluoroethylene), polypropylene, polyethylene, polystyrene, and poly(vinyl chloride) in aqueous solution as well as in organic solvent by means of electronic speckle pattern interferometry. When the polymerization is carried out in water, a clear interface appears in the vicinity of the hydrophobic substrates at a critical time when the auto-acceleration of the polymerization starts. The polymerization on the hydrophobic substrate is suppressed after the appearance of the interface which gives rise to a heterogeneous gel structure. The thickness of the substrate-induced inhomogeneous layer increases with the square root of the polymerization time, showing the feature of monomer diffusion. An enhanced heterogeneous polymerization occurs on the hydrophobic substrate with a lower surface tension. These effects are greatly suppressed when the polymerization is carried out in ethanol and in the presence of hydrophobic monomer, giving rise to a homogeneous gelation. The correlation between the surface tension of the substrates and the interface strength in water suggests that the substrate-induced interface formation might be associated with the high interfacial tension between the substrate and the polymerizing solution.
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