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首页> 外文期刊>International journal of hydrogen energy >Formic acid-ammonium formate mixture: A new system with extremely high dehydrogenation activity and capacity
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Formic acid-ammonium formate mixture: A new system with extremely high dehydrogenation activity and capacity

机译:甲酸-甲酸铵混合物:具有极高脱氢活性和容量的新系统

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Formic acid (FA) ammonium formate (AF) mixture is studied as a possible new system for dehydrogenation over a common Pd/C catalyst synthesized via a modified impregnation-NaBH4 reduction method. The composition and morphology of the Pd/C catalyst are characterized using X-ray diffraction, energy-dispersive X-ray spectroscopy, transmission electron microscopy, high-resolution transmission electron microscopy, and inductively coupled plasma atomic emission spectrometry. Results show that the initial turn-over frequency of the FA AF mixtures with total FA and AF concentration of 10 mol dm(-3) and FA molar fraction of 0.2 can reach 7959 h(-1) at 50 degrees C, which is the highest value reported for heterogeneous Pd-based catalysts in FA-based systems. FA in this mixture can completely decompose and deliver an electrochemical capacity of 565.87 mAh mL(-1). The activity and stability of the Pd/C catalyst in this system are greatly improved in comparison with those of FA sodium formate system. The excellent dehydrogenation performance of FA AF mixture can be attributed to the catalytic activity of formate toward the decomposition of FA, the effect of ammonia adsorption on Pd/C catalyst, and the higher solubility of AF in FA solution. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:甲酸(FA)甲酸铵(AF)混合物作为一种可能的新体系进行了研究,该体系可通过改性浸渍-NaBH4还原方法合成的普通Pd / C催化剂上脱氢。使用X射线衍射,能量色散X射线光谱,透射电子显微镜,高分辨率透射电子显微镜和电感耦合等离子体原子发射光谱对Pd / C催化剂的组成和形态进行表征。结果表明,在50摄氏度时,总FA和AF浓度为10 mol dm(-3)和FA摩尔分数为0.2的FA AF混合物的初始周转频率可以达到7959 h(-1)。 FA基体系中非均相Pd基催化剂的最高报道值。该混合物中的FA可以完全分解并提供565.87 mAh mL(-1)的电化学容量。与FA甲酸钠体系相比,该体系中Pd / C催化剂的活性和稳定性大大提高。 FA AF混合物的优异脱氢性能可归因于甲酸酯对FA分解的催化活性,氨在Pd / C催化剂上的吸附作用以及AF在FA溶液中的较高溶解度。 (C)2016氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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