Wu Yanbin, Joseph Sony, Aluru N R
Department of Mechanical Science and Engineering, Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, IL-61801, USA.
J Phys Chem B. 2009 Mar 19;113(11):3512-20. doi: 10.1021/jp808145x.
The present study reports on molecular dynamics investigations of chemically cross-linked poly(ethylene glycol) hydrogels with the aim of exploring the diffusion properties of water, ions, and rhodamine within the polymer at the molecular level. The water structure and diffusion properties were studied at various cross-linking densities with molecular weights of the chains ranging from 572 to 3400. As the cross-linking density is increased, the water diffusion decreases and the slowdown in diffusion is more severe at the polymer-water interface. The water diffusion at various cross-linking densities is correlated with the water hydrogen bonding dynamics. The diffusion of ions and rhodamine also decreased as the cross-linking density is increased. The variation of diffusion coefficient with cross-linking density is related to the variation of water content at different cross-linking densities. Comparison of simulation results and obstruction scaling theory for hydrogels showed similar trends.
本研究报告了化学交联聚乙二醇水凝胶的分子动力学研究,目的是在分子水平上探索聚合物内水、离子和罗丹明的扩散特性。研究了不同交联密度下链分子量范围为572至3400时的水结构和扩散特性。随着交联密度的增加,水扩散降低,且在聚合物 - 水界面处扩散减缓更为严重。不同交联密度下的水扩散与水氢键动力学相关。离子和罗丹明的扩散也随着交联密度的增加而降低。扩散系数随交联密度的变化与不同交联密度下的含水量变化有关。水凝胶模拟结果与阻碍标度理论的比较显示出相似的趋势。