Effect of different manufacturing methods on polyamide reverse-osmosis membranes for desalination: Insights from molecular dynamics simulations

被引:22
|
作者
Li, Ying [1 ]
He, Jinlong [1 ,2 ]
McCutcheon, Jeffrey R. [3 ]
机构
[1] Univ Wisconsin Madison, Dept Mech Engn, Madison, WI 53706 USA
[2] Univ Connecticut, Dept Mech Engn, Storrs, CT 06269 USA
[3] Univ Connecticut, Ctr Environm Sci & Engn, Dept Chem & Biomol Engn, Storrs, CT 06269 USA
基金
美国国家科学基金会;
关键词
Molecular layer by layer; Interfacial polymerization; Polyamide membrane; Non -equilibrium molecular dynamics; WATER DESALINATION; NANOFILTRATION MEMBRANES; COMPOSITE MEMBRANES; ACTIVE LAYERS; FORCE-FIELD; TRANSPORT; FLUX; POLYMERIZATION; PERMEABILITY; SELECTIVITY;
D O I
10.1016/j.desal.2022.116204
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Membranes are a key technology platform for a broad application of energy-efficient separations. To best serve the separation demands of industry, the manufacturing processes for these membranes are garnering increasing attention. In particular, for water desalination, the industry-leading polyamide (PA) reverse osmosis (RO) membranes can be manufactured via molecular layer-by-layer (mLBL) deposition, interfacial polymerization (IP), and 3D-printing technique. However, the influence of different manufacturing methods on PA membrane's properties is far from understood. In this study, we present the high-pressure transport behavior of water and salt ions for PA membranes formed with IP, mLBL, and 3D-printing through non-equilibrium molecular dynamics simulations. Studies show that membranes fabricated with 3D-printing have similar performances to those manufactured using mLBL, quantified by water permeability, rejection of salt ions, structural integrity, and porosity features. However, the membranes formed with IP exhibit faster water transport, lower rejection, worse structural integrity, and more inhomogeneous network pores than those constructed using mLBL and 3D -printing. The unconnected water-accessible space governs water transport for PA membranes formed with mLBL and 3D-printing, which offers the impermanent open-closed pores that enable water to jump through PA membranes. In contrast, the permeated water-enterable space plays a prominent role in water movement across the PA membrane formed with IP, providing a continuous transport channel at high pressure. Importantly, we observe the more significant compaction features at high pressure for PA membranes formed with IP than mLBL and 3D-printing. In short, these findings provide a comprehensive understanding of existing membrane prepa-ration technologies. It also provides a guide for developing the new membrane preparation process at the mo-lecular level.
引用
收藏
页数:16
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