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FORMATION OF POLYCHLORINATED DIBENZO-P-DIOXINS DIBENZOFURANS ON FLY ASH FROM PRECURSORS AND CARBON MODEL COMPOUNDS

机译:由前驱物和碳模型化合物在粉煤灰上形成多氯联苯-P-二恶英二苯并呋喃

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摘要

In this article the formation of polychlorinated dibenzo-p-dioxins (PCDD) and polychlorinated dibenzofurans (PCDF) on waste incinerator fly ash is described. Model experiments were performed by heating organic-C-free fly ash with organic model compounds. Both chlorobenzenes and phenol form PCDD and PCDF via condensation reactions. Phenol is 10-540 times as reactive as the chlorobenzenes. A second (and separate) formation pathway is from oxidative breakdown of macromolecular carbon. This route was studied with hexane, toluene and three anthraquinone derivatives as carbon model compounds. Aliphatic, monocyclic aromatic and functionalized quinone parts of carbon may all contribute to PCDD and PCDF formation, but the latter pathway appears to be the most important. Functional groups play an important role in the potential of these various carbon parts to form PCDD and PCDF. [References: 26]
机译:在本文中,描述了在垃圾焚烧炉的飞灰上形成多氯二苯并对二恶英(PCDD)和多氯二苯并呋喃(PCDF)。通过将不含有机碳的粉煤灰与有机模型化合物加热来进行模型实验。氯苯和苯酚都通过缩合反应形成PCDD和PCDF。苯酚的活性是氯苯的10-540倍。第二个(和单独的)形成途径来自大分子碳的氧化分解。使用己烷,甲苯和三种蒽醌衍生物作为碳模型化合物研究了该途径。碳的脂肪族,单环芳香族和官能化醌部分都可能促成PCDD和PCDF的形成,但后者似乎是最重要的途径。官能团在这些碳原子形成PCDD和PCDF的潜力中起着重要作用。 [参考:26]

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