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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Low temperature decomposition of PCDD/PCDF, chlorobenzenes and PAHs by TiO_2-based V_2O_5-WO_3 catalysts
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Low temperature decomposition of PCDD/PCDF, chlorobenzenes and PAHs by TiO_2-based V_2O_5-WO_3 catalysts

机译:TiO_2基V_2O_5-WO_3催化剂对PCDD / PCDF,氯苯和PAH的低温分解

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摘要

The oxidation of representative congeners of polychlorinated dibenzo-p-dioxins (PCDDs). polychlorinated dibenzofurans (PCDFs). polychlorinated chlorobenzenes (PCBzs), and of polyaromatic hydrocarbons (PAHs) was investigated on two commercial V_2O_5-WO_3/TiO_2-based catalysts, optimized for the combined reduction of nitrogen oxides and decomposition of dioxins. The non-chlorinated polyaromatic compounds (including non-chlorinated dibenzodioxin and dibenzofuran) are destroyed at temperatures as low as 150 deg C with an efficiency of more than 95%. PCDD and PCDF were also removed from the gas phase with an efficiency of >98%. However, at 150 deg C they remained mainly unchanged (up to 75%) adsorbed on the catalyst. A decrease in the oxidation rate with increasing chlorine substitution was found for the PCDD/PCDF. This could be explained by an increasing "redox potential" with increasing chlorine substitution due to the electron withdrawing effect of the chlorine. For the more volatile monoaromatic PCBz, however, the effect of lowering the volatility with increasing chlorine substitution (resulting in longer residence time on the catalyst ) over-compensates the effect of the increasing "redox potential" with higher degree of chlorination.
机译:多氯联苯对二恶英(PCDDs)代表性同类物的氧化。多氯二苯并呋喃(PCDF)。在两种基于V_2O_5-WO_3 / TiO_2的商用催化剂上研究了多氯代氯苯(PCBzs)和多环芳烃(PAHs),这些催化剂针对氮氧化物的还原和二恶英的分解进行了优化。非氯化多芳族化合物(包括非氯化二苯并二恶英和二苯并呋喃)在低至150摄氏度的温度下被破坏,效率超过95%。还从气相中去除了PCDD和PCDF,效率> 98%。然而,在150℃下,它们吸附在催化剂上基本上保持不变(最高75%)。对于PCDD / PCDF,发现氧化速率随氯取代度的增加而降低。这可以解释为由于氯的电子吸收作用而随着氯取代的增加而增加的“氧化还原电势”。然而,对于挥发性更高的单芳族PCBz,随着氯取代度的增加而降低挥发度的效果(导致更长的催化剂停留时间)过度补偿了随着氯化度增加而增加的“氧化还原电势”的影响。

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