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Photomodification of ultrafiltration membranes - Part 11 - Chemically and morphologically defined ultrafiltration membrane surfaces prepared by heterogeneous photo-initiated graft polymerization

机译:超滤膜的光改性-第11部分-通过异质光引发接枝聚合反应制备的化学和形态确定的超滤膜表面

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Polyacrylonitrile (PAN) ultrafiltration (UF) membranes with varied surface hydrophilicity and charge have been prepared by heterogeneous photo-initiated graft polymerization of various acrylates or methacrylates having polyethyleneglycol (PEG), carboxyl, sulfopropyl, dimethylaminoethyl or trimethylammoniumethyl side groups. A series of photo-modified membranes with about the same water permeabilities were obtained by selection of initial membrane pore size and appropriate modification conditions (monomer concentration and UV irradiation time, lambda(exc) > 300 nm). A comprehensive characterization of the new membranes was achieved using a multi-method approach. Gravimetry, FTIR-ATR spectroscopy, SEM and UF experiments provided basic information about the degree of graft polymer modification (DG, up to 1 mg cm(-2)) and integrity of the macroporous membrane structure after modification. No extra layer (with a thickness >1 mu m) was deposited on top of the UF membranes but, depending on DG, active layer pores were more or less covered, causing reduced water permeabilities and enhanced solute selectivities. The modified membranes were monitored with scanning force microscopy (SFM), contact angle (CA) and streaming potential (ZP) measurements. The water-swollen graft polymer layers had a monomer-specific texture with larger grain size, but in the sub-micrometer range, compared with the unmodified membranes (SFM). However, interface interactions in terms of zeta potential (ZP) and hydrophilicity (CA) were unambiguously governed by the chemistry of the graft polymer side groups. Solid surface tensions (wetting/dewetting) from advancing and receding CAs, gamma(sv) (adv.)/gamma(sv) (rec.), ranged from 35 mN m(-1)/60 mN m(-1) for PAN-grafted-poly(dimethyl-aminoethyl methacrylate) to 71.5 mN m(-1)/71.5 mN m(-1) for PAN-grafted-poly(sulfopropyl acrylate) and PAN-grafted-poly(tri-methylammoniumethyl methacrylate), whereas unmodified PAN membranes had 49 mN m(-1)/67 mN m(-1). Concentration potential measurements revealed that ion-exchange graft-polymer-modified PAN membranes behave as barrier for co-ions via a Donnan exclusion mechanism. All analytical data enabled a classification of the photo-modified UF membranes into permanently anionic (sulfonic acid) or cationic (trimethylammonium) as well as ionizable (carboxyl, dimethylamino) or non-ionic hydrophilic, flexible (PEG) types. The results provide guide-lines for the development of new low-fouling UF and nanofiltration membranes. (C) 1998 Elsevier Science B.V. [References: 25]
机译:已经通过具有聚乙二醇(PEG),羧基,磺基丙基,二甲基氨基乙基或三甲基铵乙基侧基的各种丙烯酸酯或甲基丙烯酸酯的异质光引发接枝聚合反应,制备了具有不同表面亲水性和电荷的聚丙烯腈(PAN)超滤(UF)膜。通过选择初始膜孔径和合适的修饰条件(单体浓度和紫外线照射时间,λ(exc)> 300 nm),可获得一系列具有大约相同的水渗透性的光修饰膜。使用多种方法对新膜进行了全面表征。重量分析,FTIR-ATR光谱,SEM和UF实验提供了有关接枝聚合物改性程度(DG,高达1 mg cm(-2))和改性后大孔膜结构完整性的基本信息。在UF膜的顶部没有沉积额外的层(厚度> 1μm),但是根据DG的不同,活性层的孔或多或少被覆盖了,从而降低了水的渗透性并提高了溶质的选择性。用扫描力显微镜(SFM),接触角(CA)和流动电位(ZP)测量监测改性的膜。与未改性的膜(SFM)相比,水溶胀的接枝聚合物层具有特定于单体的纹理,具有较大的晶粒尺寸,但在亚微米范围内。然而,在界面电势(ZP)和亲水性(CA)方面,接枝聚合物侧基的化学性质是明确控制的。前进和后退CA的固体表面张力(润湿/去湿),γ(sv)(adv。)/ gamma(sv)(rec。)的范围为35 mN m(-1)/ 60 mN m(-1) PAN接枝的聚(丙烯酸甲基磺丙酯)和PAN接枝的聚(甲基丙烯酸三甲基铵)的PAN接枝的聚(甲基丙烯酸二甲基-氨基乙基甲基酯)至71.5 mN m(-1)/71.5 mN m(-1),而未经修饰的PAN膜则具有49 mN m(-1)/ 67 mN m(-1)。浓度电势测量表明,离子交换接枝聚合物改性的PAN膜通过Donnan排斥机制充当了对离子的屏障。所有分析数据均能将光改性超滤膜分类为永久性阴离子(磺酸)或阳离子(三甲基铵)以及可离子化(羧基,二甲基氨基)或非离子性亲水,柔性(PEG)类型。研究结果为开发新型低污染超滤和纳滤膜提供了指导。 (C)1998 Elsevier Science B.V. [参考:25]

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