Determination of organotin compounds by headspace solid-phase microextraction-gas chromatography-pulsed flame-photometric detection (HS-SPME-GC-PFPD)

被引:38
|
作者
Bravo, M
Lespes, G
De Gregori, I
Pinochet, H
Gautier, MP
机构
[1] Univ Pau & Pays Adour, CNRS, UMR 5034, Lab Chim Analyt,LCABIE, F-64013 Pau, France
[2] Pontificia Univ Catolica Valparaiso, Inst Quim, Lab Quim Analit & Ambiental, Valparaiso 2950, Chile
关键词
organotin compounds; solid-phase microextraction; gas chromatography-pulsed flame photometric detection (GC-PFPD); experimental design; canonical analysis;
D O I
10.1007/s00216-005-0131-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A method based on Headspace solid-phase microextraction (HS-SPME, with a 100 mu m PDMS-fiber) in combination with gas-chromatography and pulsed flame-photometric detection (GC-PFPD) has been investigated for simultaneous determination of eight organotin compounds. Monobutyltin (MBT), dibutyltin (DBT), tributyltin (TBT), monophenyltin (MPhT), and the semi-volatile diphenyltin (DPhT), triphenyltin (TPhT), monooctyltin (MOcT), and dioctyltin (DOcT) were determined after derivatization with sodium tetraethylborate. The conditions used for the extraction and preconcentration step were optimised by experimental design methodology. Tripropyltin (TPrT) and diheptyltin (DHepT) were used as internal standards for quantification of volatile and semi-volatile organotin compounds, respectively. The analytical precision (RSD) for ten successive injections of a standard mixture containing all the organic tin compounds ranged between 2 and 11%. The limits of detection for all the organotin compounds were sub ng (Sn) L-1 in water and close to ng (Sn) kg(-1) in sediments. The accuracy of the method was evaluated by analysis of two certified reference material (CRM) sediment samples. The HS-SPME-GC-PFPD was then applied to the analysis of three harbour sediment samples. The results showed that headspace SPME is an attractive tool for analysis of organotin compounds in solid environmental matrices.
引用
收藏
页码:1082 / 1089
页数:8
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