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Reductive Debromination of Polybrominated Diphenyl Ethers by Zerovalent Iron

机译:零价铁对多溴联苯醚的还原脱溴作用

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摘要

Polybrominated diphenyl ethers(PBDEs)are a new class of global,persistent,and toxic contaminants,which need proper remediation technologies.PBDE degradation in the environment is not well understood.In this study,degradation of PBDEs with zerovalent iron was investigated with six BDEs,substituted with one to 10 bromines.Within 40 days 92% of BDE congener 209 was transformed into lower bromo congeners.During the initial reaction period of BDE 209(<5 days),hexa- to heptabromo BDEs were the most abundant products,but tetra- to pentabromo congeners were dominant after 2 weeks.The amount of mono- to tribromo BDEs was steadily increased during the experiments.BDEs 28,47,66,and 100 also showed a stepwise accumulation of lower bromo congeners.No oxidation products were detected in all experiments.The results showed that a stepwise debromination from n-bromo-to(n-l)-bromodiphenyl ethers was the dominant reaction in all congeners.The reaction rate constants of lower bromo BDEs decreased as the number of bromines decreased.The initial reductive debromination rate constants were positively correlated with the heats of formation of BDEs.The preferential accumulation of specific congeners was observed in the experiment with BDEs 28,47,66,and 100,where the most abundant products were BDEs 15,28,37,and 47,respectively.Reactions proceeded to form more stable and less brominated products that have lower heats of formation.Almost all the possible isomers from a specific parent BDE were found in all the experiments,which was probably due to the small difference of heat of formation between the products(2-5 kcal/mol).Reactions of all congeners proceeded fast at the initial phase(<5 days)followed by a slow reaction.The rate of reductive debromination of BDE 209 was slower with environmentally relevant sulfide minerals(iron sulfide and sodium sulfide).However,the product congener pattern,produced by sulfide mineral catalysis,was nearly similar with that of zerovalent iron treatment.This may be a possible source of lower brominated BDEs in the environment.Debromination of PBDEs by zerovalent iron has high potential values for remediation of PBDEs in the environment.
机译:多溴联苯醚(PBDEs)是一类新型的全球性,持久性和有毒污染物,需要适当的补救技术。人们对环境中PBDEs的降解还没有很好的了解。在这项研究中,研究了六种BDEs对零价铁降解PBDEs的研究。 ,被一到十个溴取代。在40天之内,有92%的BDE同源物209转化为低级溴同源物。在BDE 209的初始反应期间(<5天),六溴到七溴的BDE是最丰富的产物,但是2周后,四溴到五溴同类物占主导地位。在实验过程中,单溴到三溴溴化二苯醚的量稳定增加。溴化二苯醚28、47、66和100也显示出逐步积累的低溴同类物,未检测到氧化产物。结果表明,从n-溴到(nl)-溴二苯醚的逐步脱溴是所有同类物中的主要反应。低溴BDE的反应速率常数随着n溴的数量减少。初始还原脱溴速率常数与BDEs的形成热呈正相关。在28,47,66和100 BDEs的实验中观察到特定同类物的优先积累,其中最丰富的产物是BDE分别为15、28、37和47.反应继续形成更稳定,溴化程度更低的产物,且形成热更低。在所有实验中几乎都发现了特定母体BDE的所有可能异构体。产物之间形成的热差很小(2-5 kcal / mol)。所有同类物的反应在初始阶段(<5天)快速进行,随后发生缓慢的反应.BDE 209的还原脱溴速率为与环境相关的硫化物矿物(硫化铁和硫化钠)的反应速度较慢。但是,硫化物矿物催化产生的产物同类物模式几乎与零价铁处理相似。可能是环境中较低溴化BDE的来源。零价铁对PBDEs的脱溴对环境中PBDEs的修复具有很高的潜力。

著录项

  • 来源
    《Environmental Science & Technology》 |2005年第7期|p.2280-2286|共7页
  • 作者

    Young-Soo Keum; Qing X.Li;

  • 作者单位

    Department of Molecular Biosciences and Bioengineering,University of Hawaii,Honolulu,Hawaii 96822;

    Department of Molecular Biosciences and Bioengineering,University of Hawaii,Honolulu,Hawaii 96822;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 环境化学;
  • 关键词

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