Ulrich Konstantin, Galvosas Petrik, Kärger Jörg, Grinberg Farida
Department of Physics, Universität Leipzig, Linnstrasse 5, 04103 Leipzig, Germany.
MacDiarmid Institute for Advanced Materials and Nanotechnology, School of Chemical and Physical Sciences, Victoria University of Wellington, Wellington 6140, New Zealand.
Materials (Basel). 2012 May 24;5(5):966-984. doi: 10.3390/ma5050966.
Molecular diffusion of triblock copolymers poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) in water was studied with the help of Pulsed Field Gradient NMR in the broad range of polymer weight fractions from 0.09 to 0.8. Owing to amphiphilic nature of the molecules, these block copolymers exhibit rich self-organization properties when mixed with water. In particular, at ambient temperatures they form micelles and three liquid crystalline mesophases: cubic, hexagonal, and lamellar. The corresponding super-molecular structure formations were studied with the same block copolymer and at the same temperature. Self-assembly of molecules was shown to produce "pore-like" effects on their self-diffusion properties by imposing severe constraints on the dimensionality of propagation. Diffusion in the hexagonal phase was shown to be quasi one-dimensional in the direction parallel to the long axis of the ordered molecular rods. In the lamellar phase, diffusion was found to be quasi two-dimensional, in the plane of the lamellar structures. The observed diffusion anisotropy was attributed to the effects of the specific molecular ordering on the mesoscopic length scale.
借助脉冲场梯度核磁共振技术,在聚合物重量分数从0.09到0.8的广泛范围内,研究了三嵌段共聚物聚(环氧乙烷)-聚(环氧丙烷)-聚(环氧乙烷)在水中的分子扩散。由于分子的两亲性,这些嵌段共聚物与水混合时表现出丰富的自组装特性。特别是在环境温度下,它们形成胶束和三种液晶中间相:立方相、六方相和层状相。使用相同的嵌段共聚物并在相同温度下研究了相应的超分子结构形成。分子的自组装通过对传播维度施加严格限制,对其自扩散特性产生“孔状”影响。在六方相中,扩散在平行于有序分子棒长轴的方向上显示为准一维的。在层状相中,发现扩散在层状结构平面内为准二维的。观察到的扩散各向异性归因于介观长度尺度上特定分子有序排列的影响。