Furukawa Hidemitsu, Horie Kazuyuki, Nozaki Ryunosuke, Okada Mamoru
Department of Organic and Polymer Materials Chemistry, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei-shi, Tokyo 184-8588, Japan.
Phys Rev E Stat Nonlin Soft Matter Phys. 2003 Sep;68(3 Pt 1):031406. doi: 10.1103/PhysRevE.68.031406. Epub 2003 Sep 22.
The nature of inhomogeneities in vinylpolymer gels has hardly been clarified yet. Inhomogeneities on submicron and nanometer scales in polyacrylamide gels have been investigated by using a scanning microscopic light-scattering system and applying a general formula for an ensemble-averaged correlation function. The network structure of the gels is modified by varying the preparation conditions and can be roughly divided into two types. Swelling-induced modulation of inhomogeneities depends on the type of the network structure. At low monomer concentrations in preparation, both submicron- and nanometer-scale inhomogeneities increase with swelling. At high monomer concentrations in preparation, submicron-scale inhomogeneities increase with swelling, but nanometer-scale inhomogeneities decrease anomalously. This behavior is explained by a model of inhomogeneous network structure of vinylpolymer gels, where macrogel is formed from a large number of microgel particles.
乙烯基聚合物凝胶中不均匀性的本质尚未得到充分阐明。通过使用扫描显微镜光散射系统并应用总体平均相关函数的通用公式,对聚丙烯酰胺凝胶中亚微米和纳米尺度的不均匀性进行了研究。通过改变制备条件可以改变凝胶的网络结构,大致可分为两种类型。由溶胀引起的不均匀性调制取决于网络结构的类型。在制备过程中单体浓度较低时,亚微米和纳米尺度的不均匀性都会随着溶胀而增加。在制备过程中单体浓度较高时,亚微米尺度的不均匀性随着溶胀而增加,但纳米尺度的不均匀性却反常地减少。这种行为可以用乙烯基聚合物凝胶的非均匀网络结构模型来解释,其中大凝胶是由大量微凝胶颗粒形成的。