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Título
Optimization of a headspace solid-phase microextraction and gas chromatography/mass spectrometry procedure for the determination of aromatic amines in water and in polyamide spoons
Autor
Publicado en
Chemometrics and intelligent laboratory systems. 2014, V. 133, p. 121–135
Editorial
Elsevier
Fecha de publicación
2014-04
ISSN
0169-7439
DOI
10.1016/j.chemolab.2014.01.013
Resumen
In this work, a headspace solid-phase microextraction and gas chromatography coupledwith mass spectrometry
(HS-SPME-GC/MS) method for trace determination of primary aromatic amines was developed. The following
analytes were investigated: aniline (A), 4,4′-diaminodiphenylmethane (4,4′-MDA) and 2,4-diaminotoluene
(2,4-TDA) using 3-chloro-4-fluoroaniline (3C4FA) and 2-aminobiphenyl (2ABP) as internal standards. Prior to
extraction the analytes were derivatized in the aqueous solution by diazotation and subsequent iodination.
The derivativeswere extracted byHS-SPME using a PDMS/DVB fiber and analyzed by GC/MS. A D-optimal design
was used to study the parameters affecting the HS-SPME procedure and the derivatization step. Two experimental
factors at two levels and one factor at three levels were considered: (i) reaction time, (ii) extraction temperature,
and (iii) extraction time in the headspace. The interaction between the extraction temperature and
extraction time was considered in the proposed model. The loadings in the sample mode estimated by a
PARAFAC (parallel factor analysis) decomposition for each analyte were the response used in the design because
they are proportional to the amount of analyte extracted. The optimum conditions for the best extraction of the
analytes were achieved when the reaction time was 20 min, the extraction temperature was 50 °C and the
extraction time was 25 min. The interaction was significant.
A calibration based on a PARAFAC decomposition provided the following values of decision limit (CCα): 1.07 μgL−1
for A, 1.23 μg L−1 for 2,4-TDA and 0.83 μg L−1 for 4,4′-MDA for a probability of false positive fixed at 5%. Also, the
accuracy (trueness and precision) of the procedurewas assessed. Furthermore, all the analyteswere unequivocally
identified.
Finally, the method was applied to spiked water samples and polyamide cooking utensils (spoons). 3% (w/v)
acetic acid in aqueous solution was used as food simulant for testing migration from polyamide kitchenware.
Detectable levels of 4,4′-diaminodiphenylmethane and aniline were found in food simulant from some of the
investigated cooking utensils.
Palabras clave
Primary aromatic amines
HS-SPME-GC/MS
Derivatization
D-optimal design
PARAFAC
Migration test
Materia
Química analítica
Chemistry, Analytic
Versión del editor
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