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Mono- to Octa-Chlorinated PCDD/Fs in Stack Gas from Typical Waste Incinerators and Their Implications on Emission

机译:典型废物焚化炉烟气中的单氯到八氯的PCDD / Fs及其对排放的影响

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摘要

Mono- to octa-chlorinated dibenzo-p-dioxins and dibenzofurans (mono- to octa-CDD/Fs) were determined in 14 stack gas samples from two municipal solid waste incinerators and two medical waste incinerators. The total PCDD/F concentrations were 5.1-390 ng/Nm~3, and the mono- to trichlorinated homologues contributed 53.2-94.5% of the total concentrations. The homologue profiles were dominated by the MoCDF, ranged from 1.51 to 113.1 ng/Nm~3, and the proportion that each PCDF homologue group contributed to the total concentration decreased with increasing chlorination level. The toxic equivalent concentrations (I-TEQs) were 0.01-2.81 ng I-TEQ/Nm~3, with 2,3,4,7,8-PeCDF being the biggest contributor, at 30.6-60.0%. Correlations were found among the PCDD/PCDF ratios (D/F ratios), the degree of chlorination, and the TEQ. Stack gases with low I-TEQs had higher proportions of the less chlorinated homologues and lower D/F ratios, which could be attributed to the removal of the more chlorinated isomers by the air pollution control systems used by the incinerators. 2,8-DiCDF, 2,4,8-TrCDF, DiCDF, and TrCDF can be used as TEQ indicators for monitoring PCDD/Fs. 2,8-DiCDF and 2,4,8-TrCDF correlated well with the TEQ because they strongly correlated with 2,3,4,7,8-PeCDF, implying possible correlations in their formation mechanisms.
机译:在两个城市固体废物焚化炉和两个医疗废物焚化炉的14个烟气样品中测定了单氯到八氯二苯并对二恶英和二苯并呋喃(单CDD / FCD)。 PCDD / F的总浓度为5.1-390 ng / Nm〜3,一氯到三氯同系物占总浓度的53.2-94.5%。 MoCDF占主导地位,在1.51至113.1 ng / Nm〜3之间,随着氯化程度的增加,各PCDF同源物占总浓度的比例降低。毒性当量浓度(I-TEQs)为0.01-2.81 ng I-TEQ / Nm〜3,其中2,3,4,7,8-PeCDF贡献最大,为30.6-60.0%。在PCDD / PCDF比(D / F比),氯化程度和TEQ之间发现了相关性。具有低I-TEQ的烟道气具有较高比例的较少的氯化同系物和较低的D / F比,这可以归因于焚化炉使用的空气污染控制系统去除了较多的氯化异构体。 2,8-DiCDF,2,4,8-TrCDF,DiCDF和TrCDF可用作监视PCDD / F的TEQ指标。 2,8-DiCDF和2,4,8-TrCDF与TEQ相关性很好,因为它们与2,3,4,7,8-PeCDF密切相关,这暗示着它们的形成机理可能存在相关性。

著录项

  • 来源
    《Environmental Science & Technology》 |2013年第17期|9774-9780|共7页
  • 作者单位

    State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, P.O. Box 2871, Beijing 100085, China;

    State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, P.O. Box 2871, Beijing 100085, China;

    State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, P.O. Box 2871, Beijing 100085, China;

    State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, P.O. Box 2871, Beijing 100085, China;

    State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, P.O. Box 2871, Beijing 100085, China;

    State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, P.O. Box 2871, Beijing 100085, China;

    State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, P.O. Box 2871, Beijing 100085, China;

    State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, P.O. Box 2871, Beijing 100085, China;

  • 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);
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  • 正文语种 eng
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  • 入库时间 2022-08-17 14:02:18

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