共 30 条
Investigation of the adsorption mechanism and preconcentration of sulfonamides using a porphyrin-functionalized Fe3O4-graphene oxide nanocomposite
被引:62
作者:

Shi, Pengzhi
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h-index: 0
机构:
Capital Normal Univ, Dept Chem, Beijing 100048, Peoples R China Capital Normal Univ, Dept Chem, Beijing 100048, Peoples R China

Ye, Nengsheng
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h-index: 0
机构:
Capital Normal Univ, Dept Chem, Beijing 100048, Peoples R China Capital Normal Univ, Dept Chem, Beijing 100048, Peoples R China
机构:
[1] Capital Normal Univ, Dept Chem, Beijing 100048, Peoples R China
来源:
基金:
中国国家自然科学基金;
北京市自然科学基金;
关键词:
Adsorption;
Graphene oxide;
Magnetic solid-phase extraction;
Porphyrin;
Sulfonamides;
SOLID-PHASE EXTRACTION;
CARBON NANOTUBES;
SAMPLE PREPARATION;
ELECTROCHEMICAL DETECTION;
ANALYTICAL-CHEMISTRY;
ENVIRONMENTAL WATER;
GRAPHENE;
DOPAMINE;
SORBENTS;
COMPOSITES;
D O I:
10.1016/j.talanta.2015.05.013
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
In this work, a novel type of porphyrin-functionalized Fe3O4-graphene oxide (TCPP/Fe3O4-GO) nano-composite was synthesized. The adsorption mechanism of the prepared TCPP/Fe3O4-GO material was investigated and predicted. The pi-pi stacking and electrostatic attraction between the positively charged analytes and the negatively charged porphyrin-functionalized Fe3O4-GO accelerated the electron transfer between the materials. In addition, to investigate the preconcentration of the prepared TCPP/Fe3O4-GO, it was used as a magnetic solid-phase extraction adsorbent for the preconcentration of seven sulfonamides (SAs) from environmental water samples. Parameters that significantly affected the extraction of the SAs onto the sorbent, such as the elution solvent, extraction time and elution time, were optimized. Under the optimal conditions, the SAs in the environmental water samples were effectively detected. The linear range for the seven SAs was 0.5-20 mu g mL(-1), and the limits of detection for all seven SAs were 0.2 mu g mL(-1). Good reproducibility was obtained, along with relative standard deviations that ranged from 0.01 to 8.25%. The present method was applied to the determination of SAs in tap and river water samples, and the recoveries were satisfactory (83.7-116.7%). (C) 2015 Elsevier B.V. All rights reserved.
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页码:219 / 225
页数:7
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