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Using nitrogen isotope fractionation to assess abiotic reduction of nitroaromatic compounds

机译:使用氮同位素分级法评估硝基芳香族化合物的非生物还原

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Compound-specific isotope analysis (CSIA) is an increasingly important tool for the qualitative and quantitative assessment of transformations of organic compounds in contaminated environments. To date, the use of CSIA has been mainly restricted to the elements C and H, although N constitutes a very important reactive center for many priority contaminants. To evaluate the potential use of N isotope effects in the fate assessment of organic contaminants, we investigated the N isotope enrichment during the abiotic reduction of 4 substituted nitroaromatic compounds (NACs), using two abiotic model reductants, namely Fe(II) sorbed to goethite (alpha-FeOOH) and juglone (8-hydroxy-1,4-naphthoquinone) in the presence of H2S. Substantial and virtually identical isotope enrichment factors, epsilon(N), of about -30 parts per thousand, indicative of the breaking of one N-O bond, were found for all NACs, regardless of the reductant involved and the substitution of the NAC. These results indicate that the epsilon(N)-values determined in our study could be representative for the reduction of aromatic NO2-groups and thus be used to assess the abiotic transformation of NACs qualitatively and quantitatively in complex anoxic environments.
机译:化合物特异性同位素分析(CSIA)是定性和定量评估受污染环境中有机化合物转化的一种越来越重要的工具。迄今为止,CSIA的使用主要限于元素C和H,尽管N构成了许多重要污染物的重要反应中心。为了评估N同位素效应在命运评估有机污染物中的潜在用途,我们使用两种非生物模型还原剂,即吸附到针铁矿上的Fe(II),研究了4种取代硝基芳香族化合物(NAC)非生物还原过程中的N同位素富集。 H2S的存在下(α-FeO​​OH)和ju(8-羟基-1,4-萘醌)。对于所有NAC,发现了几乎相同的同位素富集因子ε(N),约为千分之三十,这表明NAC断裂,而与所涉及的还原剂和NAC的取代无关。这些结果表明,在我们的研究中确定的ε(N)值可以代表芳族NO 2-基团的还原,因此可用于定性和定量评估复杂缺氧环境中NAC的非生物转化。

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