磁性Fe3O4@离子印迹聚(MMA-HPMA-DVB)复合材料的合成及其对水中Ni(Ⅱ)选择性吸附

摘要

采用超声协助悬浮聚合法以Ni(Ⅱ)离子为模板制备了氨基功能化纳米Fe3O4-离子印迹聚(甲基丙烯酸甲酯(MMA)-3-(2-氨基乙基胺)-2-甲基丙烯酸羟丙酯(HPMA)-二乙烯基苯(DVB))磁性复合材料(Fe3O4@ion im-printed poly(MMA-HPMA-DVB),Fe3 O4@IIP(MMA-HPMA-DVB)).通过EA、XRD、FTIR、TEM、VSM等手段对Fe3O4@IIP(MMA-HPMA-DVB)的组成、结构、形貌、磁性等进行了表征,并研究了其吸附水中Ni(Ⅱ)的性能.结果表明:合成的Fe3O4@IIP(MMA-HPMA-DVB)平均粒径为100 nm,饱和磁化强度为43.8 emu/g;共聚单体甲基丙烯酸甲酯(MMA)的羰基通过氢键与Fe3O4表面羟基结合,有利于Fe3O4@IIP(MMA-HPMA-DVB)的核-壳结构的形成与稳定;Fe3O4@IIP(MMA-HPMA-DVB)对Ni(Ⅱ)的吸附受溶液pH值影响较小;等温吸附线符合Langmuir模型,饱和吸附量(q m,c=500 mg/g,q m,e=478 mg/g)高于非离子印迹材料(Fe3 O4@none-ion imprinted poly(MMA-HPMA-DVB),Fe3 O4@NIP(MMA-HPMA-DVB)),q m,c=90.9 mg/g,q m,e=83.8 mg/g).吸附过程可在5 min内达到平衡,符合准二级动力学模型.Fe3 O4@IIP(MMA-HPMA-DVB)能高选择性地有效吸附水中Ni(Ⅱ),对Ni(Ⅱ)的印迹因子(α)为1.9,对几种常见共存离子的选择性因子(β)>7.7,是潜在的高选择性吸附和回收Ni(Ⅱ)的功能材料.%An amino-functionalized Fe3 O4-ion imprinted poly(methyl methacrylate (MMA)-3-(2-amino-ethylami-no)-2-hydroxypropyl methacrylate (HPMA)-divinylbenzene(DVB))magnetic composite (Fe3 O4 @ion imprinted po-ly(IIP)(MMA-HPMA-DVB))was synthesized via ultrasonic assisted suspension polymerization with nickel(Ⅱ)as ion imprinting template.The Fe3 O4 @IIP(MMA-HPMA-DVB)was characterized by EA,XRD,FTIR,TEM,TG and VSM.The application for its adsorption properties on Ni(Ⅱ)from water was investigated.The results show that the Fe3 O4 @IIP(MMA-HPMA-DVB)has an average size of 100 nm,with the saturation magnetization intensity of 43.8 emu/g.The carbonyl group of the co-monomer methyl methacrylate (MMA)can connect with the hydroxyl group at the surface of the nano-Fe3 O4 via hydrogen bonds,which would be favorable to the formation and stabiliza-tion of the coreashell structure of the Fe3 O4 @IIP(MMA-HPMA-DVB).The adsorption capacities were investigated