Research Institute of Membrane Separation Technology of Shaanxi Province, Key Laboratory of Membrane Separation of Shaanxi Province, Key Laboratory of Northwest Water Resources, Environmental and Ecology, Ministry of Education, Key Laboratory of Environmental Engineering, Shaanxi Province, School of Environmental & Municipal Engineering, Xi'an University of Architecture and Technology, Yan Ta Road. No.13, Xi'an, 710055, China.
Environ Sci Pollut Res Int. 2021 Sep;28(34):46303-46318. doi: 10.1007/s11356-021-14170-4. Epub 2021 May 4.
Functionalized multiwalled carbon nanotube (f-MWCNT) mixed matrix forward osmosis (FO) membranes were fabricated by phase inversion, and the mechanism of sodium alginate (SA) membrane fouling in the presence of various inorganic components with high ionic strength was thoroughly investigated. The membrane incorporated with 0.5% f-MWCNTs (M-0.5) exhibited enhanced performance, which was attributed to the hydrophilicity of the modified nanoparticles and their good compatibility with the cellulose acetate (CA) substrate. Moreover, it was found that the initial permeate flux decline rate for all FO membranes investigated followed the order Na + Ca + Mg > Na + Ca > Na + Mg > Na, which was attributed to the particle size of SA macromolecules in the corresponding solutions. However, the gradual change in attenuation was consistent with adhesion force observations made for the SA-fouled FO membrane in the later steady-state stage, and there was little difference among M-0 (without f-MWCNTs), M-0.5, and M-1 (with 1% f-MWCNTs). Furthermore, the SA adsorption layer was most compact in the presence of Ca, and the flux recovery rate (FRR) was the lowest after simple hydraulic cleaning, but the overall FRRs for FO membranes were greater than 85%. This implies that although a decrease in electrostatic repulsion leads to the formation of a compact fouling layer, an increase in hydration repulsion of hydrated salt ions plays a major role in membrane fouling under high ionic strength conditions.
功能化多壁碳纳米管 (f-MWCNT) 混合基质正向渗透 (FO) 膜是通过相转化法制备的,并且深入研究了在高离子强度的各种无机成分存在下海藻酸钠 (SA) 膜污染的机制。含有 0.5% f-MWCNTs(M-0.5)的膜表现出增强的性能,这归因于改性纳米粒子的亲水性及其与纤维素乙酸酯 (CA) 基底的良好相容性。此外,发现所有研究的 FO 膜的初始渗透通量下降率遵循顺序 Na + Ca + Mg > Na + Ca > Na + Mg > Na,这归因于相应溶液中 SA 大分子的粒径。然而,在后期稳定阶段,随着对 SA 污染的 FO 膜的粘附力观察,衰减的逐渐变化与观察到的一致,并且在 M-0(无 f-MWCNTs)、M-0.5 和 M-1(含 1% f-MWCNTs)之间几乎没有差异。此外,在存在 Ca 的情况下,SA 吸附层最致密,经过简单的水力清洗后通量恢复率(FRR)最低,但 FO 膜的整体 FRR 大于 85%。这意味着,尽管静电排斥的降低导致形成致密的污染层,但在高离子强度条件下,水合盐离子的水化排斥的增加在膜污染中起着主要作用。