Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/10555
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dc.contributor.authorLino, Celeste M.-
dc.contributor.authorSilveira, M. Irene N.-
dc.date.accessioned2009-07-08T09:03:28Z-
dc.date.available2009-07-08T09:03:28Z-
dc.date.issued1997-07-16-
dc.identifier.citationJournal of Agricultural and Food Chemistry. 45:7 (1997) 2718-2722en_US
dc.identifier.issn0021-8561-
dc.identifier.urihttps://hdl.handle.net/10316/10555-
dc.description.abstractLosses of residues of α-hexachlorocyclohexane (α-HCH), β-HCH, γ-HCH, hexachlorobenzene (HCB), heptachlor and its epoxide, p,p‘-DDE, p,p‘-DDD, o,p‘-DDT, p,p‘-DDT, α-endosulfan, β-endosulfan, endosulfan sulfate, aldrin, dieldrin, and endrin, when linden is subjected to three infusion processes, were studied. Compounds were quantified by gas−liquid chromatography with electron capture detection. Higher losses are found for heptachlor epoxide (HE) and o,p‘-DDT, in process 1 and for α-HCH, HCB, HE, and aldrin in procedures 2 and 3. Lower losses are obtained for β-HCH in process 2. The best procedure for infusion preparation was procedure 3.en_US
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsopenAccesseng
dc.subjectPesticidesen_US
dc.subjectTilia cordata Millen_US
dc.subjectInfusion processesen_US
dc.titleLoss of Organochlorine Pesticide Residues during the Infusion Processes of Linden (Tilia cordata Mill.)en_US
dc.typearticleen_US
dc.identifier.doi10.1021/jf960941o-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.openairetypearticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.researchunitAssociated Laboratory for Green Chemistry - Clean Technologies and Processes-
crisitem.author.orcid0000-0003-1565-8756-
Appears in Collections:FFUC- Artigos em Revistas Internacionais
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