聚酰胺
反渗透
膜
纳米复合材料
化学工程
原位聚合
材料科学
高分子化学
芳纶
界面聚合
聚合
原位
聚合物
化学
有机化学
复合材料
单体
纤维
工程类
生物化学
作者
Feng‐Tao Zheng,Jian‐Bo Qu,Zhou Sun
标识
DOI:10.1016/j.memsci.2022.120914
摘要
Bis(triethoxysilyl)ethane (BTESE) nanoparticles were incorporated into aromatic polyamide (PA) membranes via in-situ polymerization to prepare BTESE nanocomposite PA (BTESE-TFN) membranes for reverse osmosis. In-situ polymerization was utilized to produce BTESE nanoparticles with high dispersion in PA membranes by adding BTESE as precursors into PA membranes for in-situ polymerization. Organic bridged -C-C- in BTESE provided enhanced compatibility between BTESE nanoparticles and PA membranes. The BTESE-TFN membranes showed durability with stable RO performance for more than 96 h because of the high dispersion of BTESE nanoparticles and enhanced compatibility between BTESE nanoparticles and PA membranes. The BTESE nanoparticles increased surface roughness, thickness, hydrophilicity of PA membranes. The BTESE nanoparticles changed surfaces of PA membranes to looser structure with more pores and gaps. However, low loadings of BTESE nanoparticles in the BTESE-TFN membranes were observed due to low reactivity of Si-OC 2 H 5 groups in BTESE. Even so, salt rejection of prepared TFN-0.12 membrane was slightly improved to 96.81%, compared with that of prepared pristine PA membrane. The TFN-0.12 membrane showed water flux of 1.6 L/(m 2 •h•bar), 25% higher than the water flux of pristine PA membrane because of enlargement of pore sizes in BTESE nanoparticles, formation of a loose and rough membrane surface and enhancement of hydrophilicity of the membrane surface. Furthermore, modification of organic bridged groups in the BTESE exhibited great potential to further optimize the water flux and durability of BTESE-TFN membranes. • Bis(triethoxysilyl)ethane nanocomposite aromatic polyamide membranes were prepared. • In-situ polymerization provided better dispersion of nanoparticles and durability. • Nanocomposite membranes showed 25% higher water flux than PA membranes. • Nanoparticles increased thickness, surface roughness, hydrophilicity of membranes.
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