聚氯乙烯平板纳滤膜的PDA界面重构与性能提升OA
PDA interface reconstruction and performance enhancement of polyvinyl chloride flat-sheet nanofiltration membranes
针对荷负电纳滤膜普遍存在的通量-截留率选择性权衡难题,提出了 PDA 界面重构策略,即以聚氯乙烯平板膜为基础,以聚多巴胺(PDA)为中间层改性聚氯乙烯(PVC)基膜,通过在 PDA 改性层表面进行哌嗪(PIP)与均苯三甲酰氯(TMC)的界面聚合,成功制备了高性能荷负电复合纳滤膜,并对水接触角、原子力显微镜(AFM)、Zeta 电位及分离性能等系统进行表征分析.结果发现:PDA 修饰显著改善了膜的亲水性,水接触角由 60.02°下降至 23.78°;膜表面粗糙度明显增加,平均粗糙度和均方根粗糙度分别提升 88.3%与 92.7%,从而有效扩展了 过 滤 面 积;表面等电点由 8.1 降至 5.2,表明负电荷密度显著增强;改性膜纯水通量达17.23 L/(m2·h),且对 MgCl2 的截留率较未改性膜提高 45.32%.
Negatively charged nanofiltration(NF)membranes,while widely employed in water treatment,face a fundamental performance limitation known as the permeability-selectivity trade-off.To overcome this challenge,this study introduces an interfacial reconstruction strategy utilizing a polydopamine(PDA)interlayer,designed to concurrently enhance the water permeability and solute selectivity of thin-film composite(TFC)NF membranes.A polyvinyl chloride(PVC)substrate was fabricated via phase inversion.First,the casting solution was prepared by the phase inversion method,consisting of 0.5%polyvinylpyrrolidone(PVP),5%polyethylene glycol 3500(PEG 3500)and 20%polyvinyl chloride(PVC),with DMAC as the solvent.After casting,the film was immersed in a deionized water coagulation bath to obtain the unmodified PVC base membrane(M0).Subsequently,PDA modification was performed on the surface of the M0 membrane:it was immersed in a 0.2 g/L dopamine solution(pH=8.8)and shaken for 1.5 hours.After cleaning and heat treatment,the PDA-modified base membrane(M1)was obtained.Finally,with M0 and M1 as the base membranes respectively,two composite nanofiltration membranes—N1(without a PDA layer)and N2(with a PDA intermediate layer)—were synthesized via the interfacial polymerization reaction between piperazine(PIP)and trimesoyl chloride(TMC).The surface properties of the membranes were characterized using techniques such as water contact angle measurement,surface roughness analysis,and Zeta potential testing,and their pure water flux and MgCl2 rejection performance were evaluated.The results demonstrate that the PDA interlayer effectively engineered the membrane's surface properties.A significant enhancement in hydrophilicity was observed,with the water contact angle decreasing from 60.02° to 23.78°.The surface roughness increased markedly,as indicated by an 88.3%and 92.7%rise in the average(Ra)and root-mean-square(Rq)roughness,respectively,which contributes to an enlarged effective filtration area.Furthermore,the surface charge property was altered,evidenced by a shift in the isoelectric point from 8.1 to 5.2,confirming a reinforcement of surface electronegativity.These synergistic modifications resulted in superior separation performance.Compared to the control N1 membrane,the N2 membrane with the PDA interlayer achieved a pure water flux of 17.23 L/(m2·h),alongside a 45.32%increase in MgCl2 rejection. This study validates that the PDA interfacial reconstruction strategy successfully mitigates the classic trade-off in NF membranes by synergistically tailoring hydrophilicity,surface charge,and morphology.The pronounced improvement in hydrophilicity is strongly correlated with the induced charge reversal.The mechanism is attributed to the catechol/quinone redox equilibrium inherent to PDA,which facilitates the formation of a surface dipole layer capable of simultaneous proton transfer and electron conduction,leading to negative charge accumulation.This strategy provides a novel and effective pathway for designing advanced high-performance negatively charged NF membranes,with promising potential for applications in high-salinity wastewater treatment,water softening,and selective separation processes.
翁可欣;钱建华;戴宏翔;林灵;单江音;王澳
浙江理工大学纺织科学与工程学院(国际丝绸学院),浙江 杭州 310018浙江理工大学纺织科学与工程学院(国际丝绸学院),浙江 杭州 310018||现代纺织技术创新中心(鉴湖实验室),浙江 绍兴 312030杭州市质量计量科学研究院,浙江 杭州 310018浙江理工大学纺织科学与工程学院(国际丝绸学院),浙江 杭州 310018浙江理工大学纺织科学与工程学院(国际丝绸学院),浙江 杭州 310018浙江理工大学纺织科学与工程学院(国际丝绸学院),浙江 杭州 310018
化学化工
亲水性能PVC纳滤膜PDA中间层界面聚合荷电性
hydrophilic performancePVC nanofiltration membranePDA middleware layerinterfacial polymerizationcharge performance
《现代纺织技术》 2026 (6)
35-42,8
中央财政引导地方科技发展资金项目(2024ZY01039)
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