催化作用
化学吸附
产量(工程)
高分辨率透射电子显微镜
活化能
扩展X射线吸收精细结构
氧烷
材料科学
化学
溶解
核化学
物理化学
吸收光谱法
光谱学
纳米技术
冶金
透射电子显微镜
物理
量子力学
生物化学
作者
Emil Sebastian Gutterød,Sigurd Øien‐Ødegaard,Koen W. Bossers,Anne‐Eva Nieuwelink,Maela Manzoli,Luca Braglia,Andrea Lazzarini,Elisa Borfecchia,S. Ahmadigoltapeh,Boris Bouchevreau,Bjørn Tore Lønstad-Bleken,Reynald Henry,Carlo Lamberti,Silvia Bordiga,Bert M. Weckhuysen,Karl Petter Lillerud,Unni Olsbye
标识
DOI:10.1021/acs.iecr.7b01457
摘要
CO2 hydrogenation was carried out over Pt-containing UiO-67 Zr-MOFs at T = 220–280 °C and ambient pressure, with H2/CO2 = 0.2–9 and contact times, τ = 0.004–0.01 gcat·min·mL–1. The catalysts were characterized by XRD, N2 adsorption, FESEM, TEM and HRTEM, Pt L3-edge XANES and EXAFS, dissolution-NMR, CO chemisorption, IR spectroscopy, and TGA. A positive correlation was observed between the degree of Pt reduction and CO2 conversion. Contact time variation experiments showed that CO is a primary product of reaction, while CH4 is a secondary product. Testing of catalyst crystals with 0.15 and 2.0 μm crystal size, respectively, revealed no influence of diffusion on the reaction rate. Comparison to a conventional Pt/SiO2 catalyst showed very similar activation energy, with Eapp = 50 ± 3 kJ·mol–1. However, the turnover frequency over Pt/SiO2 was significantly lower, and Pt/SiO2 did not yield methane as a product. The Pt-containing UiO-67 Zr-MOF catalyst showed stable activity during 60 h of testing.
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