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Preparation and evaluation of diblock copolymer-grafted silica by sequential surface initiated-atom transfer radical polymerization for reverse-phase/ion-exchange mixed-mode chromatography
被引:15
作者:
Bo, Chun Miao
[1
,2
]
Wang, Chaozhan
[1
]
Wei, Yin Mao
[1
]
机构:
[1] Northwest Univ, Coll Chem & Mat Sci, Key Lab Modern Separat Sci Shaanxi Prov, Minist Educ,Key Lab Synthet & Nat Funct Mol Chem, Xian 710127, Shaanxi, Peoples R China
[2] Ningxia Univ, Key Lab Energy & Chem Engn, Yinchuan, Peoples R China
基金:
中国国家自然科学基金;
关键词:
atom transfer radical polymerization;
diblock copolymers;
ion exchange;
mixed-mode chromatography;
stationary phases;
PERFORMANCE LIQUID-CHROMATOGRAPHY;
HYDROPHILIC INTERACTION CHROMATOGRAPHY;
STATIONARY-PHASE;
CATION-EXCHANGE;
BONDED SILICA;
SEPARATION;
COLUMN;
PEPTIDES;
D O I:
10.1002/jssc.201700719
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
A novel approach that involved the grafting of diblock copolymer with two types of monomer onto substrate by sequential surface initiated-atom transfer radical polymerization was proposed to prepare amixed-mode chromatographic stationary phase. The distinguishing feature of this method is that it can be applied in the preparation of various mixed-mode stationary phases. In this study, a new reverse-phase/ion-exchange stationary phase was prepared by grafting hydrophobic styrene and cationic sodium 4-styrenesulfonate by the proposed approach onto silica surface. The chromatographic properties of the prepared stationary phase were evaluated by the separation of benzene derivatives, anilines, and beta-agonists, and by the effect of pH values and acetonitrile content on the retention. Compared with typical RP columns, the prepared stationary phase achieved the better resolution and higher selectivity at a shorter separation time and lower organic content. Moreover, the application of the prepared column was proved by separating widely distributed polar and charged compounds simultaneously.
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页码:4700 / 4708
页数:9
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