Täuber Karoline, Zhao Qiang, Antonietti Markus, Yuan Jiayin
Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476 Potsdam, Germany.
ACS Macro Lett. 2015 Jan 20;4(1):39-42. doi: 10.1021/mz500674d. Epub 2014 Dec 18.
Highly charged porous polymer membranes with adjustable pore size and gradient pore structure along the membrane cross-section were prepared by ammonia-triggered electrostatic complexation between an imidazolium-based cationic poly(ionic liquid) (PIL) and multivalent benzoic acid derivatives. The PIL and the acid compound were first dissolved homogeneously in DMSO, cast into a thin film onto a glass plate, dried, and finally immersed into an aqueous ammonia solution. The diffusion of ammonia from the top to the bottom into the film neutralized the acid and introduced the gradient pore structure and in situ electrostatic cross-linking to fix the pores. The pore size and its distribution of the membranes were found controllable in terms of the multivalency of the acids, the imidazolium/carboxylate ratio, and the nature of the PIL counteranion.
通过基于咪唑鎓的阳离子聚离子液体(PIL)与多价苯甲酸衍生物之间的氨引发静电络合,制备了具有可调孔径和沿膜横截面的梯度孔结构的高电荷多孔聚合物膜。首先将PIL和酸化合物均匀溶解在二甲基亚砜(DMSO)中,浇铸在玻璃板上形成薄膜,干燥,最后浸入氨水溶液中。氨从顶部到底部扩散到膜中,中和了酸,并引入了梯度孔结构和原位静电交联以固定孔。发现膜的孔径及其分布可根据酸的多价性、咪唑鎓/羧酸盐比例和PIL抗衡离子的性质进行控制。