首页|对位芳香族聚酰胺复合纳滤膜制备及高温纳滤性能

对位芳香族聚酰胺复合纳滤膜制备及高温纳滤性能

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本文以对位芳香族聚醜胺(PPTA)超滤膜为基膜,无水哌嗪(PIP)与1,3,5-苯三甲酿氯(TMC)分别作为水相单体和油相单体,采用界面聚合法制得高通量耐热PPTA/PA复合纳滤膜。研究了反应条件对PPTA/PA复合纳滤膜高温纳滤性能影响,观察了复合纳滤膜表面形貌与致密层结构,考察了渗透通量、耐热性以及抗污染等性能。结果表明,当PIP浓度为15%wt,TMC浓度为2。5%wt,热处理温度和时间分别为60℃和8min时,所得PPTA/PA复合纳滤膜对不同染料分子截留率可达95%以上,对二价盐截留率可达90%以上。在高温条件下,所得PPTA/PA复合纳滤膜表现出优良的染料脱盐性能,在刚果红染料与Na2SO4截留率保持在99%的同时,渗透通量可达50L·m-2·h-1·MPa-1以上。
Preparation and thermal resistance performance for PPTA composite nanofiltration membrane
In this paper,high flux heat-resistant PPTA/PA composite nanofiltration membranes were prepared by interfacial polymerization using para-aromatic polyamide(PPTA)ultrafiltration membrane as the base membrane and Piperazine(PIP)and trimesoyl chloride(TMC)as the aqueous and oil phase monomers,respectively.The effects of interfacial polymerization on the high-temperature nanofiltration performance of PPTA/PA composite nanofiltration membranes were investigated.The surface morphology and dense layer structure of the composite nanofiltration membranes were observed,and the permeance,heat resistance and anti-pollution properties were investigated.The results showed that when the PIP concentration was 15%wt,the TMC concentration was 2.5%wt,the heat treatment temperature and time were 60℃and 8 min,respec-tively,the PPTA/PA composite nanofiltration membrane could retain more than 95%of rejection for different dye molecules and more than 90%of rejection for divalent salts,Under high temperature conditions,the obtained PPTA/PA composite nanofiltration membranes exhibited excellent dye desalination performance,and the permeate flux could reach more than 50 L·m-2·h-1·MPa-1while the rejection rate of Congo red and Na2SO4 remained at 99%.

PPTAinterfacial polymerizationnanofiltration membraneheat-resistance

王纯、赖星、颜鼎荷、付梦洁、郑文丽

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上海工程技术大学,纤维材料研究中心,上海,201620

天津工业大学,省部共建分离膜与膜过程国家重点实验室,天津,300387

中化高性能纤维材料有限公司,扬州,211400

对位芳香族聚酰胺 界面聚合 复合纳滤膜 耐高温

国家自然科学基金江苏省科技研发项目大学生创新创业训练计划项目

21808165BE20220041CX2209013

2024

环境化学
中国科学院生态环境研究中心

环境化学

CSTPCD北大核心
影响因子:1.049
ISSN:0254-6108
年,卷(期):2024.43(2)
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