Seuser Grant, Staffel Raechel, Hocaoglu Yagmur, Upton Gabriel F, Garcia Elijah S, Cronauer Donald C, Kropf A Jeremy, Martinelli Michela, Jacobs Gary
Catalyst and Aftertreatment Research and Development Group, Southwest Research Institute, 6220 Culebra Road, San Antonio, TX 78238, USA.
Department of Biomedical Engineering and Chemical Engineering, University of Texas at San Antonio, 1 UTSA Circle, San Antonio, TX 78249, USA.
Nanomaterials (Basel). 2023 Mar 24;13(7):1155. doi: 10.3390/nano13071155.
Sodium-promoted monoclinic zirconia supported ruthenium catalysts were tested for CO hydrogenation at 20 bar and a H:CO ratio of 3:1. Although increasing sodium promotion, from 2.5% to 5% by weight, slightly decreased CO conversion (14% to 10%), it doubled the selectivity to both CO (36% to ~71%) and chain growth products (4% to 8%) remarkably and reduced the methane selectivity by two-thirds (60% to ~21%). For CO hydrogenation during in situ DRIFTS under atmospheric pressure, it was revealed that Na increases the catalyst basicity and suppresses the reactivity of Ru sites. Higher basicity facilitates CO adsorption, weakens the C-H bond of the formate intermediate promoting CO formation, and inhibits methanation occurring on ruthenium nanoparticle surfaces. The suppression of excessive hydrogenation increases the chain growth probability. Decelerated reduction during H-TPR/TPR-MS and H-TPR-EXAFS/XANES at the K-edge of ruthenium indicates that sodium is in contact with ruthenium. A comparison of the XANES spectra of unpromoted and Na-promoted catalysts after H reduction showed no evidence of a promoting effect involving electron charge transfer.
对钠促进的单斜锆负载钌催化剂进行了测试,以考察其在20巴和H:CO比为3:1条件下的CO加氢性能。尽管将钠促进量从2.5重量%增加到5重量%会使CO转化率略有下降(从14%降至10%),但它使CO选择性(从36%提高到71%)和链增长产物选择性(从4%提高到8%)显著翻倍,并使甲烷选择性降低了三分之二(从60%降至21%)。对于常压下原位漫反射红外傅里叶变换光谱(DRIFTS)过程中的CO加氢反应,结果表明Na增加了催化剂的碱性并抑制了Ru位点的反应性。更高的碱性促进了CO的吸附,削弱了甲酸中间体的C-H键,促进了CO的生成,并抑制了在钌纳米颗粒表面发生的甲烷化反应。对过度加氢的抑制增加了链增长的概率。在钌的K边进行的H-程序升温还原/程序升温还原-质谱(H-TPR/TPR-MS)和H-TPR-扩展X射线吸收精细结构/ X射线吸收近边结构(H-TPR-EXAFS/XANES)过程中还原速度的减慢表明钠与钌接触。对未促进和Na促进的催化剂在H还原后的XANES光谱进行比较,没有发现涉及电子电荷转移的促进作用的证据。