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Radical polymerization initiated from a solid substrate. 2. Study of the grafting layer growth on the silica surface by in situ ellipsometry

机译:从固体底物引发自由基聚合。 2.用原位椭偏法研究二氧化硅表面的接枝层生长

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Kinetics of the grafting free radical polymerization of styrene from the surface of Si wafers with a top silica layer was studied by in situ ellipsometric measurements of the grafted amount (A). Wafers uncovered and covered by physisorbed azo- or peroxide macroinitiator or covalently bonded with the substrate azo-initiator were used. Additional initiator of the same chemical nature was added to the bath solution (bulk). It was found that the grafted amount approaches a plateau value depending on the rate of grafting polymerization. At low rates, the plateau A values are on the order of 1-2 mg/m2, whereas at high rates, they are typically 10-15 mg/m2. Two kinetic regimes were studied where (1) the surface-attached chains terminate by chain transfer to the bulk or (2) the grafted chains terminate with the bulk free radicals. The rate of polymerization for the both regimes is linearly proportional to the surface density of the initiator. Within regime 2, the rate of polymerization has inverse square root dependence on the concentration of the initiator in the bulk. Two models were applied to explain the kinetics, which provide good agreement with the experimental data.
机译:通过原位椭偏测量接枝量(A),研究了从硅片表面有二氧化硅顶层的硅片表面苯乙烯接枝自由基聚合的动力学。使用没有被物理吸附的偶氮或过氧化物大分子引发剂覆盖或覆盖的或与底物偶氮引发剂共价键合的晶片。将具有相同化学性质的另外的引发剂添加到浴溶液(本体)中。发现接枝量取决于接枝聚合的速率接近稳定值。在低速率下,平台A值约为1-2 mg / m2,而在高速率下,它们通常为10-15 mg / m2。研究了两种动力学方案,其中(1)表面连接的链通过链转移到主体而终止,或(2)接枝的链以主体自由基而终止。两种方案的聚合速率与引发剂的表面密度线性成比例。在方案2内,聚合速率对本体中引发剂的浓度具有反平方根依赖性。应用了两种模型来解释动力学,这与实验数据具有很好的一致性。

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