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Correlation between the Soret coefficient and the static structure factor in a polymer blend

机译:聚合物共混物中Soret系数与静态结构因子之间的相关性

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Mutual mass diffusion and thermal diffusion has been investigated in poly(dimethylsiloxane)/poly(ethylmethylsiloxane) (PDMS/PEMS) polymer blends of equal weight fractions. Molar masses ranged from below 1 to over 20 kg/mol. Both the mutual mass (D) and the thermal diffusion (D-T) coefficient contain a thermally activated factor with an activation temperature of 1415 K. The molar mass dependence of D-T is due to an end-group effect of the local friction coefficient. The thermal diffusion coefficient in the limit of long chains and infinite temperature is D-T(0,infinity) = -1.69 x 10(-7) cm(2)(sK)(-1). The Soret coefficient S-T of blends far enough away from a critical point is proportional to the static structure factor S(q = 0).
机译:已经在等重量分数的聚(二甲基硅氧烷)/聚(乙基甲基硅氧烷)(PDMS / PEMS)聚合物共混物中研究了相互的质量扩散和热扩散。摩尔质量从1以下到20 kg / mol以上。互质(D)和热扩散(D-T)系数都包含激活温度为1415 K的热活化因子。D-T的摩尔质量依赖性是由于局部摩擦系数的端基效应所致。在长链和无限温度范围内的热扩散系数为D-T(0,infinity)= -1.69 x 10(-7)cm(2)(sK)(-1)。距临界点足够远的共混物的Soret系数S-T与静态结构因子S(q = 0)成正比。

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