An ionic liquid doped electrochemical copolymer coating of indole and 3-methylthiophene for the solid-phase microextraction of polycyclic aromatic hydrocarbons

被引:5
|
作者
Guo, Xiafei [1 ]
Mulati, Aiziguli [1 ]
Wu, Mian [1 ]
Zhang, Jie [1 ]
Yang, Liu [1 ]
Zhao, Faqiong [1 ]
Zeng, Baizhao [1 ]
机构
[1] Wuhan Univ, Key Lab Analyt Chem Biol & Med, Minist Educ, Coll Chem & Mol Sci, Wuhan 430072, Hubei, Peoples R China
来源
RSC ADVANCES | 2017年 / 7卷 / 36期
基金
中国国家自然科学基金;
关键词
STAINLESS-STEEL WIRE; GAS-CHROMATOGRAPHY; MASS-SPECTROMETRY; POLYPYRROLE FILMS; HEADSPACE; FIBER; COMPOSITE; DERIVATIVES; EXTRACTION; ENRICHMENT;
D O I
10.1039/c7ra02372c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel poly(indole-co-3-methylthiophene)-ionic liquid (i. e., 1-allyl-3-vinylimidazolium bis((trifluoromethyl)sulfonyl)imide) (P(In-3-MeT)/IL) composite film was electrodeposited on a stainless steel wire for headspace solid phase microextraction. The obtained P(In-3-MeT)/IL coating was rough and showed a cauliflower-shape. It had high thermal stability (up to 450 degrees C) and mechanical stability and could be used for at least 180 times in solid phase microextraction (SPME) without a decrease in extraction performance. The coating exhibited high extraction capacity for some polycyclic aromatic hydrocarbons (e. g. naphthalene, 1-methylnaphthalene, acenaphthene, biphenyl, fluorene and phenanthrene) due to the strong hydrophobic and pi-pi interactions between the analytes and P(In-3MeT)/IL. Through coupling with GC, good linearity (correlation coefficients higher than 0.9994), wide linear ranges (0.05-50 mu g L-1) and low limits of detection (6.25- 25.2 ng L-1) were achieved for these analytes. The reproducibility (defined as RSD) was 3.5-5.5% and 4.5-7.2% for single fiber (n = 5) and fiber-to-fiber (n = 5), respectively. The SPME-GC method was successfully applied for the determination of three real samples, and the recoveries for standards added were 86.8-105% for mosquito-repellent incense, 89.9-110% for cigarettes and 82.3-103% for industrial lubricant.
引用
收藏
页码:22256 / 22262
页数:7
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