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PCDD/F TEQ indicators and their mechanistic implications

机译:PCDD / F TEQ指标及其机制含义

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Stack gas samples from two incinerator facilities with different operating conditions were investigated to understand how indicators of toxic equivalency (TEQ) from among the 210 polychlorinated dibenzo-p-dioxin/furan (PCDD/F) isomers varied. This effort was motivated by the need to find more easily monitored indicator compound(s) of TEQ and to reconcile the varying indicator compounds reported in the literature. The measured isomer patterns were compared with those expected from known formation mechanisms to identify the dominant mechanism(s) and explain why certain compounds are relevant TEQ indicators. Despite differences in the facility types and operating conditions, a common pattern was found for the highly chlorinated (4Cl and higher) PCDDs/Fs. A combination of chlorination/dechlorination reactions as the dominant formation mechanism for PCDF was consistent with the observed isomer patterns, whereas condensation reactions of phenolic precursors appeared to be responsible for PCDD formation. PCDF isomers, rather than the PCDD isomers, were more closely related to the TEQ measure, likely because the chlorination mechanism favors 2,3,7,8-Cl-substitution more than the phenol condensation mechanism. Unlike highly chlorinated PCDD/F isomer patterns, less chlorinated PCDD/F patterns (especially, mono- and di-CDF) were sensitive to operating conditions and facility type. Competing formation mechanisms were inferred from the variation of observed isomer distribution patterns; this sensitivity resulted in relatively low correlations of these isomers with PCDD/F TEQ values. This suggests that any use of the low-chlorinated compounds as TEQ indicators for online monitoring processes are likely best suited for plant-specific, rather than universal, applications. In addition to many of the highly chlorinated (penta-CDF, hexa-, and hepta-CDD/F) isomers being identified as strong TEQ indicators, 1 of 12 (8%), 5 of 17 (29%), and 5 of 28 (18%) of the separable tri-CDD, tri-CDF, and tetra-CDF isomers, respectively, were identified as strong (R-2 > 0.7) TEQ. indicators in both incinerators.
机译:对来自两个运行条件不同的焚化炉设施的烟气样品进行了调查,以了解210种多氯二苯并对二恶英/呋喃(PCDD / F)异构体中的毒性当量(TEQ)指标如何变化。这项工作的动机是需要找到更容易监控的TEQ指示剂化合物,并调和文献中报道的各种指示剂化合物。将测得的异构体图与已知形成机理中预期的异构体图进行比较,以确定主要机理并解释为什么某些化合物是相关的TEQ指标。尽管设施类型和操作条件有所不同,但对于高度氯化的(4Cl及更高)PCDDs / F,发现了一种常见的模式。氯化/脱氯反应的组合作为PCDF的主要形成机理与所观察到的异构体模式一致,而酚类前体的缩合反应似乎是PCDD形成的原因。 PCDF异构体而不是PCDD异构体与TEQ度量关系更紧密,这可能是因为氯化机理比苯酚缩合机理更有利于2,3,7,8-Cl取代。与高度氯化的PCDD / F异构体模式不同,氯化程度较低的PCDD / F模式(尤其是单CDF和双CDF)对操作条件和设施类型敏感。从观察到的异构体分布模式的变化推断出竞争的形成机理。这种敏感性导致这些异构体与PCDD / F TEQ值的相关性相对较低。这表明,将低氯化物用作在线监测过程的TEQ指标可能最适合特定于工厂而不是通用的应用程序。除了许多高度氯化的异构体(五元CDF,六元CDD / F和六元CDD / F)被确定为强TEQ指标外,12个中的1个(8%),17个中的5个(29%)和5个中的5个分别鉴定出28个(18%)可分离的三CDD,三CDF和四CDF异构体为强(R-2> 0.7)TEQ。两个焚化炉中的指示器。

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