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首页> 外文期刊>Journal of Catalysis >Microcalorimetric adsorption and infrared spectroscopic studies of supported nickel catalysts for the hydrogenation of diisopropylimine to diisopropylamine
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Microcalorimetric adsorption and infrared spectroscopic studies of supported nickel catalysts for the hydrogenation of diisopropylimine to diisopropylamine

机译:支持镍催化剂的微量微核性吸附和红外光谱研究,用于二异丙基二异丙基胺的氢化

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摘要

Diisopropylimine (DIPI) was used as a probe molecule to investigate the hydrogenation of C=N on the Ni/Al2O3, Ni/LaAIO and Ni/LaOx catalysts. Microcalorimetric adsorption and infrared spectroscopy were applied to determine the surface bond strengths and structures of the reactant and product. It was found that the acidic support favored the adsorption and activation of DIPI and H-2 on Ni, leading to the increased activity (TOF) for the hydrogenation of DIPI, while the basic support promoted the dehydrogenation of the amine product on Ni, being unfavorable for the hydrogenation of DIPI. In particular, the conversion of DIPI was significantly increased when isopropanol (IPA) was used as a solvent, due to the hydrogen transfer reaction (HTR) between IPA and DIPI, which was further evidenced by the infrared spectrum of co-adsorbed IPA and DIPI. (C) 2018 Elsevier Inc. All rights reserved.
机译:二异丙基亚胺(DIPI)用作探针分子,以研究Ni / Al2O3,Ni / LaaiO和Ni / Laox催化剂上的C = N的氢化。 施用微量微核吸附和红外光谱法以确定反应物和产物的表面粘合强度和结构。 发现酸性载体有利于Ni的DIPI和H-2的吸附和活化,导致DIPI氢化的活性(TOF)增加,而基本支持促进了Ni上胺产物的脱氢 不利于DIPI的氢化。 特别地,当IPA和DIPI之间的氢转移反应(HTR)使用异丙醇(IPA)作为溶剂时,DIPI的转化显着增加,该IPA和DIPI之间的氢转移反应(HTR)通过共吸收的IPA和DIPI的红外光谱进一步证明 。 (c)2018年Elsevier Inc.保留所有权利。

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