Anion exchangers with negatively charged functionalities in hyperbranched ion-exchange layers for ion chromatography

被引:24
|
作者
Uzhel, Anna S. [1 ]
Zatirakha, Alexandra V. [1 ]
Smirnov, Konstantin N. [1 ]
Smolenkov, Alexandr D. [1 ]
Shpigun, Oleg A. [1 ]
机构
[1] Lomonosov Moscow State Univ, Dept Chem, Leninskie Gory 1-3,GSP 1, Moscow 119991, Russia
关键词
Ion chromatography; Poly(styrene-divinylbenzene); Covalently-bonded anion exchanger; Hyperbranched functional layer; Negatively charged functionalities; Determination of anions; WALLED CARBON NANOTUBES; STATIONARY PHASES; MODIFIED SILICA; PERFORMANCE; COLUMNS; IONENES;
D O I
10.1016/j.chroma.2016.12.066
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Novel pellicular poly(styrene-divinylbenzene)-based (PS-DVB) anion exchangers with covalently-bonded hyperbranched functional ion-exchange layers containing negatively charged functionalities are obtained and examined. The hyperbranched coating is created on the surface of aminated PS-DVB substrate by repeating the modification cycles including alkylation with 1,4-butanediol diglycidyl ether (1,4-BDDGE), and amination of the terminal epoxide rings with methylamine (MA) or glycine (Gly). The influence of the position and the number of the layers with glycine, as well as of the total number of the layers of amine in the coating on the chromatographic properties of the obtained stationary phases is investigated. Chromatographic performance of the obtained stationary phases is evaluated using the model mixtures of inorganic and organic anions with hydroxide eluent. It is shown that the best selectivity toward weakly retained organic acids and oxyhalides is possessed by the anion exchanger obtained after 5 modification cycles, with glycine being used in the first one. Such anion exchanger packed in 25-cm long column is capable of separating 22 anions in 58 min including 7 standard anions, mono-, di- and trivalent organic acids, oxyhalides, and some other double- and triple-charged anions. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:57 / 64
页数:8
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