Zhou Gui-Hu, Xiao Feng, Xiao Ping, Wang Dong-Sheng, Duan Jin-Ming', Shi Jian, Zang Li
College of Environmental and Municipal Engineering, Xi'an University of Architecture and Technology, Xi'an 710055, China.
SKLEAC, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.
Huan Jing Ke Xue. 2013 Oct;34(10):3945-53.
In order to enhance the hydrophilicity of the membrane and improve the antifouling properties, poly (2-hydroxyethyl methacry-late) (poly(HEMA)) was grafted to the surface of the poly(vinylidene fluoride) (PVDF) membrane by using the atom transfer radical polymerization (ATRP) method. After that, ceric ammonium nitrate (CAN) as the initiator, N, N'-methylene bisacrylamide as a cross-linking agent, a zwitterionic polymer, poly (3-( methacryloylamino) propyl-dimethyl-(3-sulfopropyl) ammonium hydroxide) (poly(MPDSAH)) were successfully grafted onto the membrane surface by radical polymerization reaction. Attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM) and contact angle measuring were employed to analyze the property and the morphology of structures before and after the membrane surface-modification. The grafting density (GD) gradually increased, with the grafting time increasing, the pore size of the membrane became smaller, and the porosity decreased, but the surface hydrophilicity of membrane was significantly enhanced at the same time. The adsorption of bovine serum albumin (BSA) tests and filtration experiments were carried out to investigate anti-fouling performances of membrane before and after modification. With the GD increasing, the amount of adsorption on the film surface significantly reduced in the high-concentration BSA solution. The water contact angle (CA) decreased most, from 77. 2 degrees to 41.7 degrees within 5 s to 0, and a flux recovery ratio up to 94. 961% , when the GD reached 288. 340 microg.cm-2. Therefore, the optimal grafting time was 2 h, with the grafting density of 288. 340 microg.cm-2.
为了提高膜的亲水性并改善抗污染性能,采用原子转移自由基聚合(ATRP)法将聚(甲基丙烯酸2-羟乙酯)(聚(HEMA))接枝到聚偏氟乙烯(PVDF)膜表面。之后,以硝酸铈铵(CAN)为引发剂,N,N'-亚甲基双丙烯酰胺为交联剂,通过自由基聚合反应成功地将两性离子聚合物聚(3-(甲基丙烯酰氨基)丙基-二甲基-(3-磺丙基)氢氧化铵)(聚(MPDSAH))接枝到膜表面。采用衰减全反射傅里叶变换红外(ATR-FTIR)光谱、X射线光电子能谱(XPS)、扫描电子显微镜(SEM)和接触角测量等手段分析膜表面改性前后的结构性能和形貌。随着接枝时间的增加,接枝密度(GD)逐渐增大,膜的孔径变小,孔隙率降低,但膜的表面亲水性同时显著增强。通过牛血清白蛋白(BSA)吸附试验和过滤实验研究改性前后膜的抗污染性能。在高浓度BSA溶液中,随着GD的增加,膜表面的吸附量显著降低。当GD达到288.340μg·cm-2时,水接触角(CA)在5s内从77.2°降至41.7°,通量恢复率高达94.961%。因此,最佳接枝时间为2h,接枝密度为288.340μg·cm-2。