Yiwen Qin, Pengfei Qi, Shuang Hao, Wenxiong Shi, Jun Xiao, Jianxiao Wang, Yunxia Hu
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引用次数: 0
Abstract
The lifespan of reverse osmosis (RO) membranes is only several months when used for industrial wastewater treatment rather than several years for seawater desalination, dramatically increasing the maintenance cost of RO. Here, to improve the separation and anti-fouling performance and thus increase the lifespan of RO membranes, we developed a creative strategy to methylate RO membranes via grafting gaseous dimethylamine molecules onto polyamide (PA) of RO membrane during interfacial polymerization. The dimethylamine-grafted RO membrane achieved a high water permeance of 3.84 l m−2 h−1 bar−1 and a high NaCl rejection of 99.05% and exhibited unprecedented anti-fouling performance against small organic charged foulants, surpassing the upper-bound threshold of the other reported anti-fouling membranes and the well-known commercial anti-fouling RO membrane (DuPont FilmTec Fortilife CR100). Both experimental results and molecular dynamics simulation findings illustrate that the methylated PA has a lower absorption energy with small charged organic foulants than the pristine PA, which alleviates the foulantsʼ absorption with a lower areal density and a looser packing, and a much shallower penetration depth inside PA. Our work suggests that avoiding penetration of foulants inside PA and preventing pore blocking of PA by foulants are essential to improve the fouling resistance of RO membranes. This work contributes a new outlook on the RO membrane-fouling mechanism from the molecular levels using molecular dynamics simulation and also develops a simple and effective methylation approach to enhance the RO membrane-fouling resistance towards small charged foulants. A reverse osmosis membrane synthesized via a vapour–solid interfacial reaction demonstrates high permselectivity and exhibits good anti-fouling performance, providing a simple and effective methylation approach to enhancing membrane-fouling resistance.
反渗透膜(RO)用于工业废水处理时的寿命只有几个月,而用于海水淡化时则长达数年,这大大增加了反渗透膜的维护成本。为了提高反渗透膜的分离和防污性能,从而延长反渗透膜的使用寿命,我们开发了一种创造性的策略,在界面聚合过程中将气态二甲基胺分子接枝到反渗透膜的聚酰胺(PA)上,使反渗透膜甲基化。二甲胺接枝的反渗透膜实现了 3.84 l m-2 h-1 bar-1 的高水渗透率和 99.05% 的高 NaCl 阻隔率,并对小分子有机带电污物表现出前所未有的抗污性能,超过了其他已报道的抗污膜和著名的商业抗污反渗透膜(杜邦 FilmTec Fortilife CR100)的上限阈值。实验结果和分子动力学模拟结果都表明,与原始 PA 相比,甲基化 PA 对小电荷有机污垢物的吸收能量更低,这就减轻了污垢物的吸收,使其具有更低的面积密度和更松散的填料,在 PA 内部的渗透深度也更浅。我们的研究表明,避免污物渗透到 PA 内部以及防止污物堵塞 PA 的孔隙对于提高反渗透膜的抗污垢能力至关重要。这项研究利用分子动力学模拟从分子水平对反渗透膜污垢机理进行了新的展望,并开发了一种简单有效的甲基化方法来提高反渗透膜对小电荷污垢物的抗污垢能力。通过汽固界面反应合成的反渗透膜具有很高的渗透选择性和良好的防污性能,为提高反渗透膜的抗污能力提供了一种简单有效的甲基化方法。