dc.creatorWindmoller, CC
dc.creatorWilken, RD
dc.creatorJardim, WD
dc.date1996
dc.dateJUN
dc.date2014-12-16T11:32:01Z
dc.date2015-11-26T17:50:19Z
dc.date2014-12-16T11:32:01Z
dc.date2015-11-26T17:50:19Z
dc.date.accessioned2018-03-29T00:33:31Z
dc.date.available2018-03-29T00:33:31Z
dc.identifierWater Air And Soil Pollution. Kluwer Academic Publ, v. 89, n. 41732, n. 399, n. 416, 1996.
dc.identifier0049-6979
dc.identifierWOS:A1996UT88100012
dc.identifier10.1007/BF00171644
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/53609
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/53609
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/53609
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1289645
dc.descriptionThermal release analysis of mercury species in contaminated soils was performed by temperature controlled continuous heating of the samples in a furnace coupled to an Atomic Absorption Spectrophotometer (AAS). It was shown that this method allows the identification of different redox states of Hg-species through their characteristic releasing temperature ranges. The method was applied to Hg-contaminated samples from an inactive chlor-alkali production plant in former East Germany (GER), and from a gold mining area in Pocone, Mate Grosso, Brazil (BRA), as well as synthetic soil samples obtained by spiking pre-heated soil matrices (GER and BRA) with the following mercury species: Hg-0, Hg2Cl2, HgCl2, HgO and HgS. The samples GER, in general, frequently showed the presence of Hg2+ probably bound to humic substances, in the case of samples with higher total carbon content. Only in highly contaminated samples (>3000 ppm of mercury) was HgO the predominant species. The samples BRA more frequently showed the presence of mercury species in the lower oxidation states, i.e. Hg1+ in combination with Hg-0. The method allows observing changes in Hg-speciation in the samples with time, mainly changes among the oxidation states Hg-0, Hg1+ and Hg2+. The treated GER matrix showed a stronger tendency to oxidise Hg-species than the BRA treated matrix, in which only added HgO is partially oxidised to Hg1+ and Hg2+. In contrast, the BRA matrix showed a pronounced tendency to reduce spiked Hg2+ to Hg1+. This may be the reason for the presence of Hg1+ in the majority of original BRA samples. The method appears to be very useful to study speciation of mercury and its dynamics. It can be used as a tool for monitoring mercury oxidation states and/or reactions of mercury in soils.
dc.description89
dc.description41732
dc.description399
dc.description416
dc.languageen
dc.publisherKluwer Academic Publ
dc.publisherDordrecht
dc.publisherHolanda
dc.relationWater Air And Soil Pollution
dc.relationWater Air Soil Pollut.
dc.rightsfechado
dc.sourceWeb of Science
dc.subjectmercury speciation
dc.subjectsoil
dc.subjectthermal release analysis
dc.titleMercury speciation in contaminated soils by thermal release analysis
dc.typeArtículos de revistas


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