...
首页> 外文期刊>International Journal of Chemical Kinetics >Kinetics of Catalytic Hydrogenation of 5-Hydroxymethylfurfural to 2,5-bis-Hydroxymethylfuran in Aqueous Solution over Ru/C
【24h】

Kinetics of Catalytic Hydrogenation of 5-Hydroxymethylfurfural to 2,5-bis-Hydroxymethylfuran in Aqueous Solution over Ru/C

机译:Ru / C水溶液中5-羟甲基糠醛催化加氢生成2,5-双羟甲基呋喃的动力学

获取原文
获取原文并翻译 | 示例

摘要

5-Hydroxymethylfurfural (5-HMF) is a cellulosic product of the hydrolysis of biomass, and it is widely considered for the production of several interesting chemicals and derivatives. In the present work, catalytic hydrogenation of 5-hydroxymethylfurfural to 2,5-bis-hydroxymethylfuran was investigated using 5% Ru/C in the aqueous phase. Kinetic data were experimentally obtained over a wide range of temperatures (313-343 K), H-2 partial pressure (0.69-2.07 MPa), initial HMF concentration (19.8-59.5 mM), and catalyst loading (0.3-0.7 kg/m(3)) in a three-phase slurry reactor. Disappearance of initial 5-HMF concentrations was modeled using the power law and Langmuir-Hinshelwood-Hougen-Watson models. A model based on the competitive adsorption of molecular H-2 and HMF was proposed. It is presumed that surface reaction between nondissociatively chemisorbed H-2 and 5-HMF was rate determining. This model provided the best fit for the kinetic data. From the Arrhenius equation, the activation energy for the surface reaction was found to be 104.9 kJ/mol. (C) 2016 Wiley Periodicals, Inc.
机译:5-羟甲基糠醛(5-HMF)是生物质水解的纤维素产物,被广泛认为可用于生产几种有趣的化学品和衍生物。在本工作中,研究了在水相中使用5%Ru / C将5-羟甲基糠醛催化氢化为2,5-双-羟甲基呋喃。在宽温度范围(313-343 K),H-2分压(0.69-2.07 MPa),初始HMF浓度(19.8-59.5 mM)和催化剂负载量(0.3-0.7 kg / m)上通过实验获得了动力学数据(3))在三相淤浆反应器中。使用幂律模型和Langmuir-Hinshelwood-Hougen-Watson模型对初始5-HMF浓度的消失进行建模。提出了基于分子H-2和HMF竞争吸附的模型。推测非离解性化学吸附的H-2和5-HMF之间的表面反应是决定速率的。该模型为动力学数据提供了最佳拟合。根据阿伦尼乌斯方程,发现表面反应的活化能为104.9 kJ / mol。 (C)2016威利期刊公司

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