Xiang Yuan, Xu Rong-Guang, Leng Yongsheng
Department of Mechanical & Aerospace Engineering, The George Washington University, Washington, District of Columbia 20052, United States.
Langmuir. 2020 Jul 7;36(26):7648-7657. doi: 10.1021/acs.langmuir.0c01287. Epub 2020 Jun 17.
Polyzwitterions (PZs) are promising materials for the antifouling in reverse osmosis and nanofiltration membrane technology for water treatment. Fundamental understanding of the structure and molecular interactions involving zwitterions is crucial to the optimal design of antifouling in membrane separation. Here we employ the umbrella sampling and molecular dynamics simulations to investigate molecular interactions between sulfobetaine/carboxybetaine zwitterions and different metal ions (Na, K, and Ca) in an aqueous solution. The simulation results show that these ions can form stable or metastable contact ionic/solvent-shared-ionic pairs with zwitterions. Simulations at different grafting densities of PZ brush arrays reveal complex competitive association mechanisms, which are attributed to nonbonded electrostatic and van der Waals interactions among zwitterions, water molecules, and different metal ions in an aqueous environment. While the high-grafting density of the PZ brush array leads to a strong branch association between different zwitterions in water, this association is decreased at intermediate- and low-grafting densities due to strong zwitterion-water interactions. More importantly, adding ions into water at intermediate- and low-grafting densities further breaks down the zwitterion branch association, resulting in a randomly oriented and dispersed branch configuration with significant swelling of the polymers. The degree of swelling depends on the type of ions, which further changes the surface electrostatic potential of PZ coatings.
聚两性离子(PZs)是用于反渗透和纳滤膜技术中水处理防污的有前景的材料。对两性离子的结构和分子相互作用的基本理解对于膜分离防污的优化设计至关重要。在此,我们采用伞形采样和分子动力学模拟来研究水溶液中磺基甜菜碱/羧基甜菜碱两性离子与不同金属离子(Na、K和Ca)之间的分子相互作用。模拟结果表明,这些离子可与两性离子形成稳定或亚稳的接触离子/溶剂共享离子对。在不同接枝密度的PZ刷阵列上进行的模拟揭示了复杂的竞争缔合机制,这归因于水环境中两性离子、水分子和不同金属离子之间的非键静电和范德华相互作用。虽然PZ刷阵列的高接枝密度导致水中不同两性离子之间有很强的支链缔合,但由于两性离子与水的强相互作用,这种缔合在中低接枝密度时会降低。更重要的是,在中低接枝密度下向水中添加离子会进一步破坏两性离子的支链缔合,导致聚合物出现随机取向和分散的支链构型以及显著的溶胀。溶胀程度取决于离子类型,这进一步改变了PZ涂层的表面静电势。