Molecularly imprinted polymers on the surface of porous carbon microspheres for capturing dibenzothiophene

被引:20
|
作者
Liu, Weifeng [1 ,3 ]
Qin, Lei [1 ,2 ]
Shi, Weiping [1 ,2 ]
Chen, Lin [1 ,3 ]
Yang, Yongzhen [1 ,3 ]
Liu, Xuguang [1 ,2 ]
Xu, Bingshe [1 ,3 ]
机构
[1] Taiyuan Univ Technol, Minist Educ, Key Lab Interface Sci & Engn Adv Mat, Taiyuan 030024, Peoples R China
[2] Taiyuan Univ Technol, Coll Chem & Chem Engn, Taiyuan 030024, Peoples R China
[3] Taiyuan Univ Technol, Res Ctr Adv Mat Sci & Technol, Taiyuan 030024, Shanxi, Peoples R China
基金
对外科技合作项目(国际科技项目); 中国国家自然科学基金;
关键词
Field emission scanning electron microscopy; FTIR; BET; Barrett-Joyer-Halendal model; Adsorption isotherms; Gas chromatography; SELECTIVE RECOGNITION; ADSORPTION; DESULFURIZATION; BENZOTHIOPHENE; REMOVAL;
D O I
10.1007/s00604-016-1746-2
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A molecularly imprinted polymer (MIP) was deposited on the surface of porous carbon microspheres (MIP/p-CMSs) to obtain a sorbent for dibenzothiophene (DBT). The MIP/p-CMSs were synthesized by grafting polymerization and surface molecular imprinting using DBT as the template molecule, methacrylic acid as the functional monomer, and ethylene glycol dimethacrylate as the cross-linker. Field emission scanning electron microscopy and FTIR were used to characterize the morphology and structure of the sorbent. Additional studies included static adsorption experiments in terms of kinetics, isotherms and selective recognition adsorption. The results indicate that MIP/p-CMSs possess good recognition selectivity and affinity for DBT. The adsorption capacity reaches 123.7 mg g(-1) after 150 min. The adsorption on the heterogeneous MIP/p-CMSs was modeled with pseudo-second-order and Langmuir-Freundlich isotherms. Regeneration tests show the MIP/p-CMSs to be 10 times reusable without significant loss in adsorption capacity. The method was applied to capturing DBT from (spiked) gasoline and the results confirmed its applicability. Recoveries ranged from 93.2 % to 97.7 %.
引用
收藏
页码:1153 / 1160
页数:8
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