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Effects of Preliminary Thermal Extraction on De Novo Synthesis†

机译:初步热萃取对从头合成的影响†

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This study systematically compared the evolution of a wide selection of dioxin-relevant compounds during thermal extraction (TE) of filter dust in helium and during de novo (DN) tests in a flow of synthetic air. TE yielded a wide range of dioxin-relevant compounds; however, chlorinated aromatics appeared only in minor amounts. Laboratory DN tests were conducted on this same dust, and also after a mild, medium, or severe TE-procedure, involving final TE-temperatures of 300°C, 420°C, and 540°C, respectively. The same compounds were again analyzed. Chlorinated compounds (Cl-compounds) became predominant DN-products. For each DN-test and for each product, it was verified as to how far preliminary TE and consecutive DN each contribute to the sum of (TE + DN) products. Therefore, for each test, an individual TE- and DN- contribution level could be assigned to each compound monitored. Most oxygenated-compounds were TE-derived, suggesting that they formed from pre-existing oxygenated carbon structures, rather than from oxidation of carbonaceous matter. Conversely, Cl-compounds were typical DN-products and selectively gained importance as TE became more severe. The tests generated much more chlorobenzenes than chlorophenols, in line with the high polychlorinated dibenzofuran to polychlorinated dibenzo-p-dioxin ratio found by conventional analysis of the dust tested. The tests were designed to compare DN- and TE-products and, thus, distinguish between dioxin formation by the precursor route (i.e., formation from structurally related compounds) and the DN route (i.e., low- temperature, catalytic oxidation of the carbonaceous matrix). There was substantial difference between TE- and DN-products, the former being lean in Cl-compounds and the latter being rich. The sample tested was particularly rich in volatile matter and, hence, atypical. The procedure followed stepwise eliminates this volatile matter, so that DN-products from the original sample could be compared with those in which fixed carbon is more important. Preliminary TE strongly enhanced the relative importance of Cl-compounds and reduced that of oxygenated and hydrocarbon compounds during the consecutive DN tests.
机译:这项研究系统地比较了多种选择的二恶英相关化合物在氦气中过滤尘的热提取(TE)和合成空气流动的从头(DN)测试期间的演变。 TE产生了各种与二恶英有关的化合物。但是,氯化芳烃仅少量出现。在相同的粉尘上以及在轻度,中度或重度TE程序之后分别进行了实验室DN测试,最终的TE温度分别为300°C,420°C和540°C。再次分析相同的化合物。氯化化合物(Cl化合物)成为主要的DN产物。对于每个DN测试和每个产品,已验证了初始TE和连续DN分别对(TE + DN)产品总和的贡献程度。因此,对于每个测试,可以将单独的TE和DN贡献水平分配给所监测的每种化合物。大多数含氧化合物是TE衍生的,这表明它们是由预先存在的含氧碳结构形成的,而不是由碳质物质的氧化形成的。相反,Cl化合物是典型的DN产物,随着TE变得越来越严重,选择性地变得越来越重要。测试产生的氯苯比氯苯酚多得多,这与通过常规粉尘分析发现的高多氯二苯并呋喃与多氯二苯并对二恶英的比例相符。设计测试的目的是比较DN和TE产物,从而区分通过前体途径(即由结构相关化合物形成)形成的二恶英和DN途径(即碳质基质的低温催化氧化) )。 TE和DN产品之间存在显着差异,前者的Cl化合物含量较低,而后者的含量较高。被测样品的挥发性物质特别丰富,因此是非典型的。逐步进行的程序消除了这种挥发性物质,因此可以将原始样品中的DN产物与固定碳更为重要的那些产物进行比较。在连续的DN测试中,初步的TE大大增强了Cl化合物的相对重要性,并降低了含氧化合物和碳氢化合物的相对重要性。

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