Pd/SiO2和Ba-Pd/SiO2催化丁腈气相加氢生产丁胺

Q1 Materials Science
Y. Hao, M. Li, F. Cárdenas-Lizana, M. Keane
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引用次数: 4

摘要

研究了Pd/SiO2和Ba-Pd/SiO2上丁腈气相(1atm, 473 ~ 563 K)加氢反应。催化剂的表征包括TPR、H2/NH3化学吸附、TPD、XRD和TEM测试。Ba与Pd的掺入导致形成更小的金属纳米颗粒(7 nm vs 28 nm),由此产生(7倍)更高的H2化学吸附和降低的总表面酸度(来自NH3化学吸附/TPD)。两种催化剂均观察到与温度相关的活性最大值,并且与腈反应物的热脱附有关。当温度≥543 K时,Ba-Pd/SiO2的选择性加氢率(91 mol h−1 mol Pd -1)高于Pd/SiO2 (54 mol h−1 mol Pd -1),这是由于表面活性氢的可用性更高。较低的表面酸度有助于最大限度地减少高胺的缩合。对丁胺的反应速率和选择性超过了以前报道的气相操作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Production of Butylamine in the Gas Phase Hydrogenation of Butyronitrile over Pd/SiO2 and Ba-Pd/SiO2
Abstract The gas phase (1 atm, 473-563 K) hydrogenation of butyronitrile has been studied over Pd/SiO2 and Ba-Pd/SiO2. Catalysts characterisation involved TPR, H2/NH3 chemisorption/TPD, XRD and TEM measurements. The incorporation of Ba with Pd resulted in the formation of smaller metal nano-particles (7 nm vs. 28 nm) with a resultant (seven-fold) higher H2 chemisorption and decreased total surface acidity (from NH3 chemisorption/TPD). Temperature related activity maxima were observed for both catalysts and are associated with thermal desorption of the nitrile reactant. Exclusivity to the target butylamine was achieved at T ≥ 543 K where Ba-Pd/SiO2 delivered higher selective hydrogenation rate (91 mol h −1 mol Pd -1 ) than Pd/SiO2 (54 mol h −1 mol Pd −1 ), attributed to greater availability of surface reactive hydrogen. Lower surface acidity served to minimise condensation to higher amines. The rate and selectivity to butylamine exceed those previously reported for gas phase operation.
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来源期刊
Catalysis Structure & Reactivity
Catalysis Structure & Reactivity CHEMISTRY, PHYSICAL-
CiteScore
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