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    Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10259/4251

    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
    Rubio Martínez, LauraAutoridad UBU Orcid
    Sanllorente Méndez, SilviaAutoridad UBU Orcid
    Sarabia Peinador, Luis AntonioAutoridad UBU Orcid
    Ortiz Fernández, Mª CruzAutoridad UBU Orcid
    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
    URI
    http://hdl.handle.net/10259/4251
    Versión del editor
    http://dx.doi.org/10.1016/j.chemolab.2014.01.013
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    Attribution-NonCommercial-NoDerivatives 4.0 International
    Documento(s) sujeto(s) a una licencia Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
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    Nombre:
    Rubio-CILS_2014.pdf
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    902.5Kb
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