Platinum/Apatite Water-Gas Shift Catalysts

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• 作者：Dengyun Miao ; Andreas Goldbach ; Hengyong Xu
• 刊名：ACS Catalysis
• 出版年：2016
• 出版时间：February 5, 2016
• 年：2016
• 卷：6
• 期：2
• 页码：775-783
• 全文大小：464K
• ISSN：2155-5435

文摘

Water-gas shift (WGS) micro and membrane reactors are interesting components for compact H₂ production and purification devices, but they require catalysts with very high activity for optimum efficiency to minimize catalyst bed thickness and mass transfer limitations. On the other hand, activation of H₂O is known to be more challenging than CO in this reaction. Catalysts comprising ca. 2 nm large Pt particles on hydrophilic apatites are found to have very high WGS activity, with specific reaction rates exceeding those of a highly active Pt/CeO₂ catalyst by up to 50% at 573 K. These apatite-supported catalysts exhibit stable CO conversions at 673 K without showing any CH₄ formation tendencies up to 723 K. WGS activity increases with Ca/P ratio in the apatite, leveling off around Ca/P ≈ 1.75, and formate has been identified as the main reaction intermediate. The outstanding WGS performance is attributed to the superior activation of H₂O on these ionic oxides due to coordination of H₂O to Lewis acidic Ca²⁺ ions and H bonding to basic O atoms of PO₄^3– units. This renders H₂O molecules highly polarized and thus reactive on apatite surfaces with the ensuing formate-like intermediates being well stabilized through bonding to multiple Ca²⁺ ions, as well. Thus, apatites provide an intriguing alternative to increasingly expensive rare-earth oxides in high-performance noble-metal WGS catalysts not only for micro and membrane reactors.