Kim DK, Lee SB, Doh KS
Department of Chemical Engineering, Soongsil University, Seoul, 156-743, South Korea
J Colloid Interface Sci. 1998 Sep 15;205(2):417-422. doi: 10.1006/jcis.1998.5606.
The fluorosilicone copolymers were synthesized using a fluorine-containing monomer and silicone-containing monomers by free-radical random copolymerization, and their surface properties and surface modification ability were investigated. The fluorine-containing monomer used was perfluoroalkyl ethyl acrylate (FA), and the silicone-containing monomers used were 3-[tris(trimethylsilyloxy)silyl]propyl methacrylate (SiMA), vinyltrimethoxy silane (VTMS), and vinyltriethoxy silane (VTES). The surface free energies of the fluorosilicone copolymers prepared were estimated from the contact angle data measured by sessile-drop method. And, the surface free energies of poly(vinyl chloride) (PVC) films modified by the fluorosilicone copolymers were also analyzed using the contact angle data. The fluorosilicone copolymers exhibit the surface free energies of about 8-23 dyn/cm dependent on the molecular weight of the fluorosilicone copolymers. The surface free energies of the fluorosilicone copolymers decrease with increasing molecular weight in the range of 2,000-10,000 (Mw). Among the fluorosilicone copolymers prepared in this study, PFA-r-PSiMA was found to be the most effective as a surface modification agent for PVC film. The inherent surface free energy of PFA-r-PSiMA was estimated to be about 9.0 dyn/cm. The desirable molecular weight of PFA-r-PSiMA seems to be more than 4,000 (Mw). However, it is expected that the fluorosilicone copolymers having the molecular weight of much higher than 10,000 (Mw) may not be suitable as surface modification additives because their compatibility with other polymers will decrease with the molecular weight. The optimum concentration of PFA-r-PSiMA added to PVC film is about 1.0 wt.%. PFA-r-PSiMA is expectedto be an effective additive for surface modification of PVC films. Copyright 1998 Academic Press.
通过自由基无规共聚反应,使用含氟单体和含硅单体合成了氟硅氧烷共聚物,并对其表面性质和表面改性能力进行了研究。所用的含氟单体为丙烯酸全氟烷基乙酯(FA),所用的含硅单体为甲基丙烯酸3-[三(三甲基硅氧基)硅基]丙酯(SiMA)、乙烯基三甲氧基硅烷(VTMS)和乙烯基三乙氧基硅烷(VTES)。通过静滴法测量的接触角数据估算了所制备的氟硅氧烷共聚物的表面自由能。并且,还使用接触角数据分析了由氟硅氧烷共聚物改性的聚氯乙烯(PVC)薄膜的表面自由能。氟硅氧烷共聚物的表面自由能约为8-23达因/厘米,这取决于氟硅氧烷共聚物的分子量。在2000-10000(Mw)范围内,氟硅氧烷共聚物的表面自由能随分子量的增加而降低。在本研究中制备的氟硅氧烷共聚物中,发现PFA-r-PSiMA作为PVC薄膜的表面改性剂最有效。PFA-r-PSiMA的固有表面自由能估计约为9.0达因/厘米。PFA-r-PSiMA的理想分子量似乎大于4000(Mw)。然而,预计分子量远高于10000(Mw)的氟硅氧烷共聚物可能不适合作为表面改性添加剂,因为它们与其他聚合物的相容性会随着分子量的增加而降低。添加到PVC薄膜中的PFA-r-PSiMA的最佳浓度约为1.0 wt.%。PFA-r-PSiMA有望成为PVC薄膜表面改性的有效添加剂。版权所有1998年学术出版社。