Methane partial oxidation under periodic reaction conditions on Pt/Al2O3

被引:3
作者
Solanki, Surya Pratap S. [1 ,2 ]
Gan, Zhuoran [3 ]
Marino, Silvia [3 ]
Davis, Robert J. [3 ]
Epling, William S. [3 ]
Grabow, Lars C. [1 ,2 ]
机构
[1] Univ Houston, William A Brookshire Dept Chem & Biomol Engn, Houston, TX 77204 USA
[2] Univ Houston TcSUH, Texas Ctr Superconduct, Houston, TX 77204 USA
[3] Univ Virginia, Dept Chem Engn, Charlottesville, VA 22903 USA
基金
美国国家科学基金会;
关键词
WATER-GAS-SHIFT; SUPPORTED PLATINUM CATALYSTS; GAMMA-ALUMINA; REACTION-MECHANISMS; PALLADIUM; OXIDE; KINETICS; ACTIVATION; DFT; CONSEQUENCES;
D O I
10.1039/d3re00554b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The increasing interest in utilizing methane, the primary component of natural gas, for chemical production has spurred research into methane partial oxidation (MPO) as an alternative to traditional steam methane reforming (SMR). MPO has lower energy requirements and potential for carbon capture, making it an attractive option for hydrogen production. Challenges remain, however, such as carbon deposition leading to degradation and achieving high hydrogen selectivity. Here, the impact of periodic reactor operation on MPO over a Pt/Al2O3 catalyst was studied, primarily via varying reactor inlet compositions. Experiments were conducted using periodic operation strategies to assess the influence of changing reactant inlet concentrations on hydrogen formation during MPO. The results suggest that cycling between mixtures with low and high oxygen content can lead to transient hydrogen formation rates that surpass those achieved at steady state. Control experiments and density functional theory (DFT) calculations show that enhanced hydrogen formation can be attributed to the reaction between CO with hydroxyl groups at the metal and alumina support interface. This work underscores the critical role of surface coverages at the metal-support interface and suggests avenues for future exploration, including alternative support materials with higher OH mobility and changes in the cycling scheme to enhance catalyst performance under periodic conditions.
引用
收藏
页码:1489 / 1498
页数:10
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