PVDF/PI阳离子交换膜的制备及脱盐性能
作者:王乾杰,李红海,苏保卫
单位: 1.青岛科技大学 化工学院,山东青岛 266042;2.中国海洋大学 化学化工学院,青岛 266100
关键词: 阳离子交换膜;表面修饰;电渗析;浸没沉淀相转化;交联
DOI号:
分类号: TQ028.8
出版年,卷(期):页码: 2021,41(1):1-9

摘要:
通过浸没沉淀相转化的方法制备了聚偏氟乙烯(PVDF)/聚酰亚胺(PI)共混膜,然后使用4,4’-二氨基二苯乙烯-2,2’-二磺酸与三乙胺(DASD-TEA)溶液修饰共混膜表面,制备出PVDF/PI阳离子交换膜。探究了DASD-TEA溶液的浸泡时间、浸泡温度、浓度与PI的浓度对PVDF/PI阳离子交换膜脱盐率的影响,得出最优的铸膜液配比为19.0 wt%的 PVDF、1.0 wt%的PI和80.0 wt% 的N,N-二甲基甲酰胺(DMF);最佳的 DASD-TEA溶液修饰条件:0.03 wt% 的DASD,浸泡时间为10.0 min,浸泡温度为50.0 ℃。最佳条件下,PVDF/PI阳离子交换膜的离子交换容量(IEC)为0.32 mmol·g-1,含水率为38.6 %,纯水渗透率为50 L·m-2·h-1·bar-1,接触角为81.9 °,膜面电阻为2.96 Ω·cm2。采用三组膜对的电渗析装置在电压4V和流量40 L/h下对2000 mg/L NaCl溶液进行了120 min的脱盐试验,PVDF/PI阳离子交换膜的脱盐率为商品化阳离子交换膜的1.33倍,其脱盐性能高于商品化阳离子交换膜。
 Polyvinylidene fluoride (PVDF)/Polyimide (PI) blend membrane was prepared by the immersion precipitation phase transformation method. Then the PVDF/PI membrane was modified using 4,4'-diaminostilbene-2,2'-disulfonic acid and triethylamine (DASD-TEA) aqueous solution to prepare PVDF/PI cation exchange membrane. The effects of soaking time, temperature, concentration of DASD-TEA solution and PI concentration on the desalination rate of the PVDF/PI cation exchange membrane were explored. The optimal composition of the casting solution is 19.0 wt% PVDF, 1.0 wt% PI and 80.0 wt% N, N-dimethylformamide (DMF). The optimal conditions of the DASD-TEA modification are 0.03 wt% DASD in the DASD-TEA aqueous solution, and soaking at 50.0 ℃ for 10 min. The ion exchange capacity (IEC) of the PVDF/PI cation exchange membrane is 0.32 mmol·g-1, the water content is 38.6%, the pure water permeability is 50 L·m-2·h-1·bar-1, the contact angle is 81.9 °, and the transmembrane resistance is 2.96 Ω·cm2. The desalination experiment was carried out in the electrodialysis device with three membrane pairs under 4 V voltage for 120 min, with 2000 mg/L NaCl solution as feed at a flow rate of 40 L·h-1. The desalination rate of the PVDF/PI cation exchange membrane is 1.33 times that of the commercial cation exchange membrane.。

基金项目:

作者简介:
王乾杰(1994-),男,山东聊城人,硕士研究生,研究方向:传质与分离工程,E-mail: wqjqust@163.com。

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