Determination of carboxylic acids in water by gas chromatography–mass spectrometry after continuous extraction and derivatisation
► A new approach for the determination of 35 carboxylic acids in water samples is presented. ► Miniaturisation of the sample treatment system using a continuous solid-phase extraction unit. ► Simplification of the derivatising reaction through the use of a household microwave oven that reduces the r...
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Published in | Talanta (Oxford) Vol. 93; pp. 224 - 232 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier B.V
15.05.2012
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | ► A new approach for the determination of 35 carboxylic acids in water samples is presented. ► Miniaturisation of the sample treatment system using a continuous solid-phase extraction unit. ► Simplification of the derivatising reaction through the use of a household microwave oven that reduces the reaction time to ca. 3min. ► Successful analysis of drinking and natural waters.
This paper describes a new approach for the determination of monocarboxylic, dicarboxylic and tricarboxylic acids (35 compounds) in water. The analytes, in acid medium (pH ∼1.3), were sorbed on an 80mg LiChrolut EN–Supelclean ENVI-18 (1:1) column and subsequently eluted with methanol. After evaporation of the extract to ∼10μL, the analytes were spiked with 60μL of the derivatising reagent and derivatised in a household microwave oven for 3min. Among the reagents tested (BF3/1-butanol; acetyl chloride/1-butanol; isobutyl chloroformate/1-butanol; trimethylphenylammonium hydroxide, N,O-bis-(trimethylsilyl)acetamide, N,O-bis-(trimethylsilyl)trifluoroacetamide and trimethylchlorosilane), the best results in terms of reaction yield and stability of the derivatives were obtained with the mixture of 1% trimethylchlorosilane in N,O-bis-(trimethylsilyl)trifluoroacetamide. Microwave assisted derivatisation was used as an alternative heating approach for the rapid silylation of carboxylic acids. The proposed method proved to be a suitable analytical procedure for several types of carboxylic acids in water, with limits of detection within the range 0.6–15ngL−1, precision values from 4.0 to 6.0% (as within-day relative standard deviation) and recoveries from 93 to 101% for all the target analytes. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0039-9140 1873-3573 |
DOI: | 10.1016/j.talanta.2012.02.022 |