Roth C B, Pound A, Kamp S W, Murray C A, Dutcher J R
Department of Physics and the Guelph-Waterloo Physics Institute, University of Guelph, N1G 2W1, Guelph, Ontario, Canada.
Eur Phys J E Soft Matter. 2006 Aug;20(4):441-8. doi: 10.1140/epje/i2006-10034-0. Epub 2006 Sep 7.
We have used transmission ellipsometry to measure the glass transition temperature, T(g), of freely-standing films of atactic and syndiotactic poly(methyl methacrylate) (PMMA). We have prepared films with different molecular weights, MW, (159 x 10(3) < M (w) < 1.3 x 10(6)) and film thicknesses, h, ( 30 nm < h < 200 nm). For the high-MW ( M (w) > 509 x 10(3)) atactic PMMA films, we find that T(g) decreases linearly with decreasing h, which is qualitatively similar to previous results obtained for high-MW freely-standing polystyrene (PS) films. However, the overall magnitude of the T(g) reduction is much less (by roughly a factor of three) for the high-MW freely-standing PMMA films than for freely-standing PS films of comparable MW and h. The observed differences between the freely-standing PMMA and PS film data suggest that differences in chemical structure determine the magnitude of the T(g) reduction and we discuss the possible origins of these differences. Our analysis of the MW-dependence of the T(g) reductions suggests that the mechanism responsible for the MW-dependent T(g) reductions observed in the high-MW freely-standing films is different than that responsible for the MW-independent T(g) reductions observed in the low-MW freely-standing and supported films.
我们使用透射椭圆偏振光谱法测量了无规和间同立构聚甲基丙烯酸甲酯(PMMA)自支撑薄膜的玻璃化转变温度T(g)。我们制备了具有不同分子量MW(159×10³<Mw<1.3×10⁶)和薄膜厚度h(30nm<h<200nm)的薄膜。对于高分子量(Mw>509×10³)的无规PMMA薄膜,我们发现T(g)随h的减小而线性降低,这在定性上与先前对高分子量自支撑聚苯乙烯(PS)薄膜获得的结果相似。然而,高分子量自支撑PMMA薄膜的T(g)降低的总体幅度比具有可比Mw和h的自支撑PS薄膜小得多(大约小三倍)。自支撑PMMA薄膜和PS薄膜数据之间观察到的差异表明,化学结构的差异决定了T(g)降低的幅度,我们讨论了这些差异的可能来源。我们对T(g)降低的分子量依赖性的分析表明,在高分子量自支撑薄膜中观察到的与分子量相关的T(g)降低的机制不同于在低分子量自支撑和支撑薄膜中观察到的与分子量无关的T(g)降低的机制。