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悬浮聚合法制备亲水-亲油型高分子固相萃取填料及其功能化研究 被引量:2

Preparation of Hydrophilic-Lipophilic Composite Solid Phase Extraction Material by Suspension Polymerization and Its Functionalization
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摘要 采用悬浮聚合法合成了一种以二乙烯苯和N-乙烯吡咯烷酮为单体的高分子聚合物固相萃取填料(DVB-NVP),系统地考察了引发剂、致孔剂、分散剂以及反应时间等对填料形态和粒径分布的影响,用光学显微镜对其进行表征,以农药作为模型化合物,结合紫外分光光度(UV)和高效液相色谱法(HPLC)对填料进行评价。同时对合成的微球进行官能团衍生,并优化衍生化条件。结果表明:以羟丙基甲基纤维素为分散剂,偶氮二异丁腈为引发剂时,于80℃下反应8h可制得粒径为20~60μm的单分散高交联亲水-亲油型聚合物,其对灭多威、福美林以及乙酰甲胺磷的回收率分别为97.34%、86.24%和96.96%,相对标准偏差分别为2.27%、0.96%、1.83%。4种衍生化DVB-NVP填料具有较高的离子交换容量。 A hydrophilic-lipophilic balance solid phase extraction material was synthesized by suspension polymerization based on divinylbenzene and N-vinyl pyrrolidone(DVB-NVP).Several factors including various initiators,porogens,dispersing agents and react time were investigated to further enhance the characteristics of packings.The morphosis of the microspheres was tested by electron microscope and its performance as a kind of solid phase extraction(SPE)resin was evaluated using pesticide residues combined with high-performance liquid chromatography(HPLC)and ultraviolet spectrophotometry(UV).Then,the copolymer DVB-NVP was functionalized to modify the surface properties.The results indicated that the copolymer DVB-NVP with 20μm to 60μm could be obtained satisfactorily when the azobisisobutyronitrile was as the initiator,the HPMC was the dispersing agents,and the reaction time was 8hin 80°C.When real samples were pretreated by the prepared microspheres,the recovery for methomyl,thiram and acephate was 97.34%,86.24% and 96.96%,respectively,and the RSD% was 2.27%,0.96% and1.83%,respectively.For the four functionalized resins,their ion exchange capacities were able to similar,even be superior to commercial products.
出处 《材料导报》 EI CAS CSCD 北大核心 2015年第20期1-7,共7页 Materials Reports
基金 国家自然科学基金(21375093) 高等学校博士学科点专项科研基金(20130032120081) 天津大学自主创新基金(1102213)
关键词 亲水-亲油平衡 高分子聚合物 固相萃取 悬浮聚合法 功能化 hydrophilic-lipophilic balance high molecular polymer solid phase extraction suspension polymerization functionalization
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  • 1Haginaka J. Drug determination in serum by liquid chroma-tography with restricted access stationary phases [J].Trends Analytic Chem,1991,10:17.
  • 2Ruiz-Gil L,Romero-Gonzalez R, Frenich AG,et al. Deter-mination of pesticides in water samples by solid phase ex-traction and gas chromatography tandem mass spectrometry[J]_ J Separation Sci, 2008,31 : 151.
  • 3Nguyen T D, Yun M Y,Lee G H. A multiresidue methodfor the determination of 118 pesticides in vegetable juice bygas chromatography-mass spectrometry and liquid chroma-tography- tandem mass spectrometry [J]. J Agric FoodChem,2009,57(21):10095.
  • 4张庆庆,王燕燕,孟品佳.季铵盐类农药残留检测前处理研究进展[J].材料导报,2014,28(7):85-89. 被引量:7
  • 5Navare A,Zhou M S,McDonald J,et al. Serum biomarkerprofiling by solid-phase extraction with particle-embeddedmicro tips and matrix-assisted laser desorption/ionizationmass spectromertry [J]. Rapid Commun Mass Spectrome-try,2008,22:997.
  • 6Jal P K,Patel S,Mishra B K. Chemical modification of sili-ca surface by immobilization of functional groups for extrac-tive concentration of metal ions [J]. Talanta,2004,62(5):1005.
  • 7Wang S,Zhang R. Column preconcentration of lead inaqueous solution with macroporous epoxy resin-based poly-mer monolithic matrix[J]. Analytica Chimica Acta, 2006,575(2):166.
  • 8陈晓华,汪群杰.固相萃取技术与应用[M].北京:科学出版社,2010:23.
  • 9Ascenzo G D,Gentuli A,Marches S,et al. Simultaneousdetermination of base/neutral and acid herbicides in naturalwater at the part per trillion level [J], J Chromatography,1998,48:497.
  • 10包建民,谢丹,孙超慧,李优鑫,王俊菊.一种亲水-亲油复合固相萃取填料的制备及其在食品安全检测中的应用[J].色谱,2013,31(9):825-830. 被引量:8

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