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dc.creatorMachado, Ana Maria de Resende-
dc.creatorCardoso, Maria das Graças-
dc.creatorEmídio, Elissandro Soares-
dc.creatorPrata, Vanessa de Menezes-
dc.creatorDórea, Haroldo Silveira-
dc.creatorAnjos, Jeancarlo Pereira dos-
dc.creatorMagriotis, Zuy Maria-
dc.creatorNelson, David Lee-
dc.date.accessioned2019-10-08T20:38:01Z-
dc.date.available2019-10-08T20:38:01Z-
dc.date.issued2012-
dc.identifier.citationMACHADO, A. M. de R. et al. Experimental design methodology to optimize the solid phase micro-extraction procedure prior to GC-MS determination of ethyl carbamate in samples of homemade cachaça (LANL-2011-1073). Analytical Letters, [S.l.], v. 45, n. 10, p. 1143-1155, 2012. DOI: 10.1080/00032719.2012.673101.pt_BR
dc.identifier.urihttps://www.tandfonline.com/doi/full/10.1080/00032719.2012.673101pt_BR
dc.identifier.urihttp://repositorio.ufla.br/jspui/handle/1/37129-
dc.description.abstractSeeking to improve the quality of cachaça, the Ministério da Agricultura, Pecuária e Abastecimento (Ministry of Agriculture, Livestock and Supply - MAPA), the body responsible for setting and approving regulations governing the Identity and Quality Standards (PIQs) for distilled sugar cane spirits and cachaça, through the Normative Instruction No. 13 of 2005 included some contaminants such as ethyl carbamate (EC), acrolein, lead, and arsenic that must be evaluated in these drinks. Studies on EC, as well as the methods for its determination, are required to evaluate and determine which factors contribute to the formation of this compound in the beverage. An analytical method using gas chromatography/mass spectrometry (GC/MS) with prior sample treatment by solid phase microextraction (SPME) was developed along with the assessment of the principal validation parameters. These two developments lead to the determination of EC with analytical reliability. The optimization of the extraction step was performed via a factorial design involving the selection of parameters such as extraction time, extraction temperature, salt concentration, desorption time, pH, and the method of extraction. The linear range was 5.0 to 200.0 µg L−1 (R2 = 0.9965) with limits of detection and quantification of 1.5 and 5.0 µg L−1, respectively. The recoveries for samples of cachaça containing 10.0 and 80.0 µg L−1 concentrations of EC were 89% and 93%, respectively. The concentrations of EC in the samples of cachaça examined were well below the limits required by Brazilian law.pt_BR
dc.languageen_USpt_BR
dc.publisherTaylor & Francispt_BR
dc.rightsrestrictAccesspt_BR
dc.sourceAnalytical Letterspt_BR
dc.subjectCachaçapt_BR
dc.subjectEthyl carbamatept_BR
dc.subjectGC/MSpt_BR
dc.subjectSPMEpt_BR
dc.subjectGas chromatography-mass spectrometrypt_BR
dc.subjectSolid phase microextractionpt_BR
dc.titleExperimental design methodology to optimize the solid phase micro-extraction procedure prior to GC-MS determination of ethyl carbamate in samples of homemade cachaça (LANL-2011-1073)pt_BR
dc.typeArtigopt_BR
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