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One-step methyl isobutyl ketone (MIBK) synthesis from 2-propanol: Catalyst and reaction condition optimization

机译:2-丙醇一步合成甲基异丁基酮(MIBK):催化剂和反应条件的优化

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摘要

A gas-phase process for methyl isobutyl ketone (MIBK) synthesis from 2-propanol in one-pot is studied as an alternative to the conventional technology for producing MIBK from acetone (DMK). Bifunctional copper/acid-base catalysts able to operate at mild temperatures and atmospheric pressure were prepared and characterized by measuring the acid and base properties as well as the metal dispersion. It was found that a Cu-Mg-Al mixed oxide catalyst gives high MIBK yields. In this catalyst, the metal fraction in loadings of 2-6 wt% promotes the hydro-dehydrogenation steps at high rates whereas the surface acid-base sites of moderate acid and base properties favor the aldol condensation reaction. The effect of different operational conditions such as reaction temperature and reactant partial pressure was also investigated. The MIBK formation rate was enhanced by increasing 2-propanol partial pressure in a wide range, consistently with a positive 2-propanol reaction order in the overall kinetics whereas the presence of hydrogen in the reactant mixture inhibited MIBK synthesis due to a negative order with respect to H-2. An increase of the reaction temperature and the use of inert atmosphere improved the MIBK yield. By operation at 533 K in N-2 the Cu-Mg-Al catalyst with 6.4 wt% Cu, yields 27% MIBK in comparison to the 30% typically obtained in current commercial liquid-phase high-pressure processes from DMK. (c) 2006 Elsevier B.V. All rights reserved.
机译:研究了用一锅法从2-丙醇合成甲基异丁基酮(MIBK)的气相方法,作为由丙酮(DMK)制备MIBK的常规技术的替代方法。制备了能够在温和的温度和大气压下运行的双功能铜/酸碱催化剂,并通过测量酸和碱性质以及金属分散体对其进行了表征。发现Cu-Mg-Al混合氧化物催化剂产生高的MIBK产率。在该催化剂中,以2-6wt%的负载量的金属分数以高速率促进加氢-脱氢步骤,而中等酸和碱性质的表面酸碱位有利于醛醇缩合反应。还研究了不同操作条件如反应温度和反应物分压的影响。通过在较宽的范围内增加2-丙醇分压可以提高MIBK的生成速率,这与整体动力学中的正2-丙醇反应顺序一致,而反应混合物中氢的存在则由于相对于负序抑制了MIBK的合成到H-2。反应温度的提高和惰性气氛的使用提高了MIBK的产率。通过在N-2中在533 K下操作,具有6.4 wt%Cu的Cu-Mg-Al催化剂可产生27%MIBK,而在目前的工业液相高压方法中通常是从DMK获得30%的MIBK。 (c)2006 Elsevier B.V.保留所有权利。

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