Finding a suitable catalyst for on-board ethanol reforming using exhaust heat from an internal combustion engine

材料科学 催化作用 空间速度 化学工程 蒸汽重整 燃烧 制氢 贵金属 化学 金属 冶金 有机化学 工程类 选择性
作者
Albert Casanovas,Núria J. Divins,Alberto Rejas,Ricard Bosch,Jordi Llorca
出处
期刊:International Journal of Hydrogen Energy [Elsevier]
卷期号:42 (19): 13681-13690 被引量:23
标识
DOI:10.1016/j.ijhydene.2016.11.197
摘要

Ethanol steam reforming with pure ethanol and commercial bioethanol (S/C = 3) was carried out inside the housing of the exhaust gas pipe of a gasoline internal combustion engine (ICE) by using exhaust heat (610–620 °C). Various catalytic honeycombs loaded with potassium-promoted cobalt hydrotalcite and with ceria-based rhodium–palladium catalysts were tested under different reactant loads. The hydrogen yield obtained over the cobalt-based catalytic honeycomb at low load (F/W < 25 mLliq·gcat−1·h−1, GHSV = 4·102 h−1) was remarkably high, whereas that obtained over the noble metal-based catalytic honeycombs was much superior at high loads (F/W = 25–150 mLliq·gcat−1·h−1, GHSV = 4·102–2.4·103 h−1). At higher reactant loads the overall hydrogen production was limited by heat transfer from the exhaust heat to the reformer inside the housing of the exhaust gas pipe of the ICE. Extensive carbon deposition occurred over the cobalt-based honeycomb, making its use impractical. In contrast, stability runs (>200 h) at high load (F/W = 150 mLliq·gcat−1·h−1, GHSV = 2.4·103 h−1) showed that promotion of the ceria-supported noble metal catalyst with alumina and zirconia is a key element for practical application using commercial bioethanol. HRTEM analysis of post mortem honeycombs loaded with RhPd/Ce0.5Zr0.5O2–Al2O3 showed no carbon formation and no metal agglomeration.

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