De Guzman Manuel Reyes, Ang Micah Belle Marie Yap, Huang Shu-Hsien, Huang Qing-Yi, Chiao Yu-Hsuan, Lee Kueir-Rarn
Material Corrosion and Protection Key Laboratory of Sichuan Province, School of Materials Science and Engineering, Sichuan University of Science and Engineering, Zigong 643000, China.
R&D Center for Membrane Technology and Department of Chemical Engineering, Chung Yuan Christian University, Taoyuan 32023, Taiwan.
Polymers (Basel). 2021 Feb 12;13(4):544. doi: 10.3390/polym13040544.
Thin-film composite (TFC) polyamide membranes formed through interfacial polymerization can function more efficiently by tuning the chemical structure of participating monomers. Accordingly, three kinds of diamine monomers were considered to take part in interfacial polymerization. Each diamine was reacted with trimesoyl chloride (TMC) to manufacture TFC polyamide nanofiltration (NF)-like forward osmosis (FO) membranes. The diamines differed in chemical structure; the functional group present between the terminal amines was classified as follows: aliphatic group of 1,3-diaminopropane (DAPE); cyclohexane in 1,3-cyclohexanediamine (CHDA); and aromatic or benzene ring in m-phenylenediamine (MPD). For FO tests, deionized water and 1 M aqueous sodium sulfate solution were used as feed and draw solution, respectively. Interfacial polymerization conditions were also varied: concentrations of water and oil phases, time of contact between the water-phase solution and the membrane substrate, and polymerization reaction time. The resultant membranes were characterized using attenuated total reflectance-Fourier transform infrared spectroscopy, field emission scanning electron microscopy, atomic force microscopy, and surface contact angle measurement to identify the chemical structure, morphology, roughness, and hydrophilicity of the polyamide layer, respectively. The results of FO experiments revealed that among the three diamine monomers, CHDA turned out to be the most effective, as it led to the production of TFC NF-like FO membrane with optimal performance. Then, the following optimum conditions were established for the CHDA-based membrane: contact between 2.5 wt.% aqueous CHDA solution and polysulfone (PSf) substrate for 2 min, and polymerization reaction between 1 wt.% TMC solution and 2.5 wt.% CHDA solution for 30 s. The composite CHDA-TMC/PSf membrane delivered a water flux () of 18.24 ± 1.33 LMH and a reverse salt flux () of 5.75 ± 1.12 gMH; therefore, / was evaluated to be 0.32 ± 0.07 (g/L).
通过界面聚合形成的薄膜复合(TFC)聚酰胺膜可以通过调整参与聚合的单体的化学结构来更高效地发挥作用。因此,考虑了三种二胺单体参与界面聚合。每种二胺都与均苯三甲酰氯(TMC)反应,以制备TFC聚酰胺纳滤(NF)型正向渗透(FO)膜。这些二胺的化学结构不同;末端胺之间存在的官能团分类如下:1,3 - 二氨基丙烷(DAPE)的脂肪族基团;1,3 - 环己二胺(CHDA)中的环己烷;间苯二胺(MPD)中的芳香族或苯环。对于FO测试,分别使用去离子水和1 M硫酸钠水溶液作为进料液和汲取液。界面聚合条件也有所变化:水相和油相的浓度、水相溶液与膜基材的接触时间以及聚合反应时间。使用衰减全反射 - 傅里叶变换红外光谱、场发射扫描电子显微镜、原子力显微镜和表面接触角测量对所得膜进行表征,以分别确定聚酰胺层的化学结构、形态、粗糙度和亲水性。FO实验结果表明,在三种二胺单体中,CHDA是最有效的,因为它导致制备出具有最佳性能的TFC NF型FO膜。然后,为基于CHDA的膜确定了以下最佳条件:2.5 wt.% 的CHDA水溶液与聚砜(PSf)基材接触2分钟,以及1 wt.% 的TMC溶液与2.5 wt.% 的CHDA溶液之间进行30秒的聚合反应。复合CHDA - TMC/PSf膜的水通量()为18.24±1.33 LMH,反向盐通量()为5.75±1.12 gMH;因此,/ 评估为0.32±0.07(g/L)。