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Optical vs. direct sorption and swelling measurements for the study of stiff-chain polymer-penetrant interactions

机译:光学与直接吸附和溶胀测量,用于研究硬链聚合物-渗透剂相互作用

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摘要

This work involves interferometric `optical thickness¿ and refractive index measurements performed in an optical thickness meter (OTM), on supported cellulose acetate (CA) films equilibrated with various activities of methylene chloride (MC) vapor. The relevant equilibrium sorption and volume swelling isotherms were determined by application of the Claussius-Mossotti equation on the assumption that these films swell unidimensionally along the thickness direction, and were compared with corresponding direct equilibrium sorption (weight gain), elongation and thickness dilation measurements on similar free films performed in a vacuum sorption/swelling apparatus (VSA) and complemented with refractive index data. Combined elongation and thickness dilation data from the VSA showed that free glass-cast CA films exhibit pronounced swelling anisotropy. The said anisotropy, although it cannot be completely eliminated, by conditioning at high degrees of swelling, does not appear to affect the extent of volume swelling significantly, thus permitting quantitative comparison of sorption and swelling isotherms determined by the VSA and the OTM. Such comparison showed satisfactory agreement between these two sets of results up to an MC uptake of ca. 0.4 gMC/cm3 of dry CA corresponding to a degree of swelling of ca. 0.2. Increasing discrepancies are observed at higher MC concentrations, which are attributable to breakdown of the assumption used that the supported films swell unidimensionally along the thickness direction. The present CA-MC volume swelling data exhibit the negative deviation from volume additivity on mixing typical glassy polymers
机译:这项工作涉及在光学测厚仪(OTM)中对平衡有二氯甲烷(MC)蒸气各种活性的支撑的醋酸纤维素(CA)薄膜进行的“光学厚度”和折射率测量。在假定这些薄膜沿厚度方向一维溶胀的前提下,通过应用Clausius-Mossotti方程确定了相关的平衡吸附和体积溶胀等温线,并将其与相应的直接平衡吸附(重量增加),伸长率和厚度膨胀测量值进行了比较。在真空吸附/溶胀装置(VSA)中执行的类似的自由膜,并补充有折射率数据。来自VSA的伸长率和厚度膨胀数据相结合,显示出免费的玻璃铸造CA膜表现出明显的溶胀各向异性。尽管通过高度溶胀不能完全消除所述各向异性,但似乎并未显着影响体积溶胀程度,因此可以定量比较由VSA和OTM确定的吸附和溶胀等温线。这样的比较显示两组结果之间令人满意的一致性,直到MC摄取约。 0.4 gMC / cm3的干燥CA对应于溶胀度。 0.2。在较高的MC浓度下,观察到的差异越来越大,这归因于对所用薄膜沿厚度方向一维膨胀的假设的推论。当前的CA-MC体积溶胀数据显示出在混合典型的玻璃状聚合物时与体积加性的负偏差

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