Macrocyclic polyamine-modified poly(glycidyl methacrylate-co-ethylene dimethacrylate) monolith for capillary electrochromatography
文献类型:期刊论文
作者 | Tian, Yun1; Yang, Fangxing2; Yang, Xuemei1; Fu, Enqin1; Xu, Ying2; Zeng, Zhaorui1 |
刊名 | ELECTROPHORESIS
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出版日期 | 2008-06-01 |
卷号 | 29期号:11页码:2293-2300 |
关键词 | capillary electrochromatography macrocyclic polyamine methacrylate-based monolith |
ISSN号 | 0173-0835 |
通讯作者 | Zeng, ZR, Wuhan Univ, Dept Chem, Wuhan 430072, Peoples R China |
中文摘要 | 1,4,10,13,16-Pentaazatricycloheneicosane-9,17-dione (macrocyclic polyamine)-modified polymer-based monolithic column for CEC was prepared by ring opening reaction of epoxide groups from poly(glycidyl methacrylate-co-ethylene dimethacrylate) (GMA-co-EDMA) monolith with macrocyclic polyamine. Conditions such as reaction time and concentration of macrocyclic polyamine for the modification reaction were optimized to generate substantial EOF and enough chromatographic interactions. Anodic EOF was observed in the pH range of 2.0-8.0 studied due to the protonation of macrcyclic polyamine at the surface of the monolith. Morphology of the monolithic column was examined by SEM and the incorporation of macrocyclic polyamine to the poly(GMA-co-EDMA) monolith was characterized by infrared (IR) spectra. Successful separation of inorganic anions, isomeric benzenediols, and benzoic acid derivatives on the monolithic column was achieved for CEC. In addition to hydrophobic interaction, hydrogen bonding and electrostatic interaction played a significant role in the separation process. |
英文摘要 | 1,4,10,13,16-Pentaazatricycloheneicosane-9,17-dione (macrocyclic polyamine)-modified polymer-based monolithic column for CEC was prepared by ring opening reaction of epoxide groups from poly(glycidyl methacrylate-co-ethylene dimethacrylate) (GMA-co-EDMA) monolith with macrocyclic polyamine. Conditions such as reaction time and concentration of macrocyclic polyamine for the modification reaction were optimized to generate substantial EOF and enough chromatographic interactions. Anodic EOF was observed in the pH range of 2.0-8.0 studied due to the protonation of macrcyclic polyamine at the surface of the monolith. Morphology of the monolithic column was examined by SEM and the incorporation of macrocyclic polyamine to the poly(GMA-co-EDMA) monolith was characterized by infrared (IR) spectra. Successful separation of inorganic anions, isomeric benzenediols, and benzoic acid derivatives on the monolithic column was achieved for CEC. In addition to hydrophobic interaction, hydrogen bonding and electrostatic interaction played a significant role in the separation process. |
WOS标题词 | Science & Technology ; Life Sciences & Biomedicine ; Physical Sciences |
学科主题 | Biochemical Research Methods; Chemistry, Analytical |
类目[WOS] | Biochemical Research Methods ; Chemistry, Analytical |
研究领域[WOS] | Biochemistry & Molecular Biology ; Chemistry |
关键词[WOS] | PERFORMANCE LIQUID-CHROMATOGRAPHY ; STATIONARY PHASES ; ELECTROPHORETIC SEPARATION ; COLUMN ; POLYMER ; ACIDS ; DIOXOPOLYAMINE ; RECEPTOR ; ANIONS ; MEDIA |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000257011600008 |
公开日期 | 2010-10-13 |
源URL | [http://ir.ihb.ac.cn/handle/152342/8088] ![]() |
专题 | 水生生物研究所_中科院水生所知识产出(2009年前)_期刊论文 |
作者单位 | 1.Wuhan Univ, Dept Chem, Wuhan 430072, Peoples R China 2.Chinese Acad Sci, State Key Lab Freshwater Ecol & Biotechnol, Inst Hydrobiol, Wuhan, Peoples R China |
推荐引用方式 GB/T 7714 | Tian, Yun,Yang, Fangxing,Yang, Xuemei,et al. Macrocyclic polyamine-modified poly(glycidyl methacrylate-co-ethylene dimethacrylate) monolith for capillary electrochromatography[J]. ELECTROPHORESIS,2008,29(11):2293-2300. |
APA | Tian, Yun,Yang, Fangxing,Yang, Xuemei,Fu, Enqin,Xu, Ying,&Zeng, Zhaorui.(2008).Macrocyclic polyamine-modified poly(glycidyl methacrylate-co-ethylene dimethacrylate) monolith for capillary electrochromatography.ELECTROPHORESIS,29(11),2293-2300. |
MLA | Tian, Yun,et al."Macrocyclic polyamine-modified poly(glycidyl methacrylate-co-ethylene dimethacrylate) monolith for capillary electrochromatography".ELECTROPHORESIS 29.11(2008):2293-2300. |
入库方式: OAI收割
来源:水生生物研究所
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