Convenient, inexpensive quantification of elemental sulfur by simultaneous in situ reduction and colorimetric detection.

Autor: Kwasniewski MT; Department of Food Science, Cornell University, Geneva, NY, USA., Allison RB, Wilcox WF, Sacks GL
Jazyk: angličtina
Zdroj: Analytica chimica acta [Anal Chim Acta] 2011 Oct 03; Vol. 703 (1), pp. 52-7. Date of Electronic Publication: 2011 Jul 19.
DOI: 10.1016/j.aca.2011.07.010
Abstrakt: Rapid, inexpensive, and convenient methods for quantifying elemental sulfur (S(0)) with low or sub-μgg(-1) limits of detection would be useful for a range of applications where S(0) can act as a precursor for noxious off-aromas, e.g., S(0) in pesticide residues on winegrapes or as a contaminant in drywall. However, existing quantification methods rely on toxic reagents, expensive and cumbersome equipment, or demonstrate poor selectivity. We have developed and optimized an inexpensive, rapid method (∼15 min per sample) for quantifying S(0) in complex matrices. Following dispersion of the sample in PEG-400 and buffering, S(0) is quantitatively reduced to H(2)S in situ by dithiothreitol and simultaneously quantified by commercially available colorimetric H(2)S detection tubes. By employing multiple tubes, the method demonstrated linearity from 0.03 to 100 μg S(0) g(-1) for a 5 g sample (R(2)=0.994, mean CV=6.4%), and the methodological detection limit was 0.01 μg S(0) g(-1). Interferences from sulfite or sulfate were not observed. Mean recovery of an S(0) containing sulfur fungicide in grape macerate was 84.7% with a mean CV of 10.4%. Mean recovery of S(0) in a colloidal sulfur preparation from a drywall matrix was 106.6% with a mean CV of 6.9%. Comparable methodological detection limits, sensitivity, and recoveries were achieved in grape juice, grape macerate and with 1g drywall samples, indicating that the methodology should be robust across a range of complex matrices.
(Copyright © 2011 Elsevier B.V. All rights reserved.)
Databáze: MEDLINE
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