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首页> 外文期刊>Journal of the Taiwan Institute of Chemical Engineers >Ozone-catalytic oxidation for gaseous 1,2-dichloroethane in air over Pt/Al2O3 catalyst
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Ozone-catalytic oxidation for gaseous 1,2-dichloroethane in air over Pt/Al2O3 catalyst

机译:Pt / Al2O3催化剂上空气中臭氧催化氧化气态1,2-二氯乙烷

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The catalytic oxidation of 1,2-dichloroethane (DCEA) using Pt/Al2O3 with and without ozone (noted as OZCO and COXI, respectively) was carried considering the key operation parameters of reaction temperature (T), space velocity (SV) of catalyst and inlet concentration of O-3 (C-O3). The results indicate that OZCO decreases the reaction temperature and enhances the conversion of DCEA (X) to form CO2, HCI and Cl-2 comparing with COXI. At 200 ppmv CO3 and 125,000 1/h SV, 50% and 90% conversions of DCEA via OZCO are achieved at 430 and 610 K, while those via COXI are reached at 582 or 640 K, respectively. The mineralization of carbon in DCEA to form CO2 (Y-CO2) with ozone (e.g. 90% at 620 K) is systematically higher than that without ozone (e.g. 60% at 620 K). The conversions of chlorine atom in DCEA to Cl in HCl and Cl-2 are about 62.5% and 37% for OZCO at 625 K with -100% Y-CO2, which are higher than 51.5% and 10.3% for COXI at 645 K with 97% Ycov respectively. Thus the conversions of carbon and chlorine are near completion, indicating the effectiveness of OZCO for destructing the chlorine-containing pollutant of DCEA. (C) 2015 Taiwan Institute of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
机译:考虑到催化剂的反应温度(T),空速(SV)等关键操作参数,分别在有和没有臭氧的情况下,使用Pt / Al2O3催化氧化1,2-二氯乙烷(DCEA)。和O-3(C-O3)的入口浓度。结果表明,与COXI相比,OZCO降低了反应温度并增强了DCEA(X)的转化形成CO2,HCl和Cl-2的能力。在200 ppmv的CO3和125,000 1 / h SV下,通过OZCO的DCEA的转化率分别在430和610 K时达到50%和90%,而通过COXI的DCEA分别在582或640 K时达到。在DCEA中,含臭氧的碳的矿化形成二氧化碳(Y-CO2)(例如在620 K下为90%)比不含臭氧的碳的矿化(例如在620 K下为60%)高。 DCA中的氯原子到HCl和Cl-2中的Cl转化为625 K和-100%Y-CO2时的OZCO约为62.5%和37%,高于645 K和645 K时COXI的51.5%和10.3%。 Ycov分别为97%。因此,碳和氯的转化已接近完成,表明OZCO能够有效破坏DCEA的含氯污染物。 (C)2015台湾化学工程师学会。由Elsevier B.V.发布。保留所有权利。

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