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Possible alkylation...
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Yin, YongguangState Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, China
(författare)
Possible alkylation of inorganic Hg(II) by photochemical processes in the environment
- Artikel/kapitelEngelska2012
Förlag, utgivningsår, omfång ...
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Elsevier,2012
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printrdacarrier
Nummerbeteckningar
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LIBRIS-ID:oai:DiVA.org:oru-38436
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https://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-38436URI
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https://doi.org/10.1016/j.chemosphere.2012.01.006DOI
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https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-193847URI
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Språk:engelska
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Sammanfattning på:engelska
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Ämneskategori:ref swepub-contenttype
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Ämneskategori:art swepub-publicationtype
Anmärkningar
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sponsors:National Basic Research Program of China Grant no: 2009CB421605 Key Project of the National Science & Technology Pillar Program Grant no: 2006BAK03A14 National Natural Science Foundation of China Grant no:s 20807047 20907062 20937002
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The methylation of inorganic Hg by anaerobic bacteria in aquatic environments is considered to be the major pathway for methylmercury (MeHg) production. However, recent research has suggested that abiotic or chemical methylation by humic substances and other low-molecular-weight organic compounds in natural environments is also possible. Here, the aqueous photo-transformation of Hg(2+) to organomercurials was investigated in the presence of ketones, aldehydes and low molecular weight organic acids under UV irradiation. MeHg and/or ethylmercury (EtHg) were identified as the main organomercurial products by multiple analytical techniques, including chromatography-atomic spectrometry and molecular mass spectrometry and further confirmed by stable isotope tracer experiments. The yield of organomercurials was markedly influenced by pH, NaCl concentration, alkylation donor concentration and the presence of chelating ligands in the aqueous solution. Electron paramagnetic resonance spectrometry demonstrated that the radical reaction was not the predominating alkylation pathway, although methyl radicals were detected in the photo-alkylation procedure. A mechanism based on intra-molecular alkyl transfer in the Hg(2+)-low-molecular-weight organic compound complex is proposed. The present work helps us better understand of MeHg and EtHg photo-generation in natural environments.
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Chen, BaoweiState Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, China
(författare)
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Mao, YuxiangDepartment of Chemistry & Biochemistry, Florida International University, Miami FL, United States
(författare)
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Wang, Thanh,1979-State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, China(Swepub:liu)thawa68
(författare)
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Liu, JingfuState Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, China
(författare)
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Cai, YongDepartment of Chemistry & Biochemistry, Florida International University, Miami FL, United States; Southeast Environmental Research Center, Florida International University, Miami FL, United States
(författare)
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Jiang, GuibinState Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, China
(författare)
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State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, ChinaDepartment of Chemistry & Biochemistry, Florida International University, Miami FL, United States
(creator_code:org_t)
Sammanhörande titlar
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Ingår i:Chemosphere: Elsevier88:1, s. 8-160045-65351879-1298
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