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Product distribution analysis of the hydrogen peroxide direct synthesis in an isothermal batch reactor

机译:等温间歇反应器中过氧化氢直接合成的产物分布分析

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摘要

The direct synthesis of hydrogen peroxide from molecular hydrogen and oxygen on a supported palladium catalyst was studied at 258-297 K in a laboratory-scale batch reactor. The catalyst was in the form of finely dispersed slurry in methanol/CO2 to suppress the internal and external mass transfer resistances. Experiments carried out under kinetic control revealed that hydrogen peroxide was successfully formed on the catalyst surface, but it was hydrogenated as the reaction time was prolonged. The mass balances of the components were considered in detail and a reaction mechanism was proposed, based on the competitive adsorption of hydrogen and oxygen on the palladium surface. The surface reactions leading to the formation of hydrogen peroxide and water were assumed to be rate determining, and the rate equations describing direct synthesis, water formation as well as peroxide hydrogenation and decomposition were derived. A special kind of product distribution analysis was used to interpret the kinetic phenomena and to make the estimation of the kinetic parameters very robust. The parameters were estimated by nonlinear regression analysis and the model gave a good fit to the experimental data. The usefulness of the product distribution analysis was clearly demonstrated. (C) 2014 Elsevier B.V. All rights reserved.
机译:在实验室规模的间歇反应器中,研究了在负载钯催化剂上由分子氢和氧直接合成过氧化氢的过程,反应速度为258-297K。催化剂为在甲醇/ CO2中精细分散的浆料形式,以抑制内部和外部的传质阻力。在动力学控制下进行的实验表明,过氧化氢成功地形成在催化剂表面上,但是随着反应时间的延长它被氢化。基于氢和氧在钯表面上的竞争性吸附,详细考虑了组分的质量平衡并提出了反应机理。假定导致过氧化氢和水形成的表面反应是速率决定因素,并推导了描述直接合成,水形成以及过氧化物加氢和分解的速率方程。使用一种特殊的产品分布分析来解释动力学现象并使动力学参数的估计非常可靠。通过非线性回归分析估计参数,该模型与实验数据非常吻合。产品分布分析的有用性得到了明确证明。 (C)2014 Elsevier B.V.保留所有权利。

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