...
首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Kinetics of 10% Pd/C-catalysed hydrogenolysis of chlorobenzene dissolved in n-heptane by gaseous hydrogen in contact with aqueous NaOH or water
【24h】

Kinetics of 10% Pd/C-catalysed hydrogenolysis of chlorobenzene dissolved in n-heptane by gaseous hydrogen in contact with aqueous NaOH or water

机译:气态氢与NaOH水溶液或水接触时10%Pd / C催化的正庚烷中溶解的氯苯氢解的动力学

获取原文
获取原文并翻译 | 示例
           

摘要

The kinetics of the hydrogenolysis of chlorobenzene by gaseous hydrogen in the presence of 10% Pd/C catalyst was investigated in two-phase systems:n-heptane containing the substrate and the chromatographic reference substance (n-dodecane) (upper phase),and aq.NaOH or water (lower phase).The main product was benzene although traces of diphenyl were always found in post-reaction mixtures.The kinetics of hydrogenolysis followed a model of zero-order reaction when the catalyst was pre-conditioned in the upper phase.If pre-conditioning of the catalyst took place in aq.NaOH or water,the kinetics followed a model of parallel zero-order and first-order reactions.Zero-order rate constants for a catalyst pre-conditioned in the upper phase increase with the rpm (revolutions per minute) and the size of the stirring bar,whereas they first rise but then fall with increasing NaOH concentration in the lower phase.A knowledge of rate constants enables reaction completion times to be determined.The results of the kinetic analysis suggest that the main contribution to the zero-order pathway is due to the features of the catalyst surface and the transport of catalyst grains from water to the organic phase.The first-order contribution arises from the adsorption and desorption of reactants on the catalyst surface,and diffusion.The proposed approach forms a convenient framework within which to consider and design the catalytic hydrodechlorination of chlorobenzene under various conditions.
机译:在两相体系中研究了气态氢在10%Pd / C催化剂存在下通过气态氢进行氯苯氢解的动力学:两相体系:含有基质和色谱参考物质(正十二烷)(上相)的正庚烷;以及NaOH水溶液或水(下层相)。主要产物是苯,尽管在反应后混合物中总是发现痕量二苯。当催化剂在上层中进行预处理时,氢解动力学遵循零级反应模型如果在NaOH或水中进行催化剂的预处理,则动力学遵循平行的零阶和一阶反应模型。在上相中进行预处理的催化剂的零阶速率常数会增加随转速(每分钟转数)和搅拌棒的大小而变化,然后随着下部相中NaOH浓度的增加,它们先上升然后下降。了解速率常数可以确定反应完成时间。动力学分析表明,对零级路径的主要贡献是由于催化剂表面的特征以及催化剂颗粒从水到有机相的传输。一阶贡献是由于催化剂的吸附和解吸。所提出的方法为在各种条件下考虑和设计氯苯的催化加氢脱氯反应提供了一个方便的框架。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号