The Kinetic Consequences of Water on Catalytic Methane Pyrolysis

Hydrogen production from biomass and natural gas has emerged as a prominent research area in response to the growing demand for energy from alternative sources that minimize CO<sub>2</sub> emissions. In this study, we investigate the impact of water, which is present in and generated from biomass-derived streams, on carbon nanotube (CNT) growth and hydrogen production during methane decomposition using Ni-Mo/MgO as a catalyst. We reveal here that the role of water on CNT growth is highly complex; its effect depends on the stage of growth at which the water is incorporated. When water is introduced at the beginning of methane decomposition (<i>t</i> = 0 h), methane conversion rates are negatively impacted. We hypothesize that water inhibits the significant phase changes the Ni-Mo/MgO catalyst undergoes during catalyst carburization. In contrast, the incorporation of a small percentage of water after a stabilization period (<i>t</i> = 3 h) results in methane conversion rate enhancements that scale with the introduced water partial pressure as water selectively reacts with amorphous carbon deposits that lead to catalyst deactivation, thus prolonging the lifetime of some of the most active sites. Moreover, water incorporation after stabilization significantly reduces the apparent activation energy. Density Functional Theory (DFT) calculations reveal that water preferentially interacts with carbon fragments on the catalyst surface to remove carbon deposits with a barrier lower than that required for methane activation, further supporting its role in cleaning active sites on the catalyst surface. Characterization of the resulting carbon nanotubes reveals the formation of more graphitic materials produced in the presence of water, highlighting the impact of water on nanotube properties. These results provide clarity toward the many ways in which water, or cofeeding of biomass-derived materials, may impact catalytic methane pyrolysis rates.

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Publication Details

Journal
ACS Catalysis
Published
2026-02-26
DOI
https://doi.org/10.1021/acscatal.6c00011
Primary Topic
Catalysts for Methane Reforming
Type
article
Field-Weighted Citation Impact
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article

The Kinetic Consequences of Water on Catalytic Methane Pyrolysis

Laura A. Gomez, Daniel E. Resasco, Steven Crossley, Caleb Bavlnka et al.
ACS Catalysis
Catalysts for Methane Reforming
article

The Kinetic Consequences of Water on Catalytic Methane Pyrolysis

Laura A. Gomez, Daniel E. Resasco, Steven Crossley, Caleb Bavlnka, Ismaeel Alalq, Phuong T. Nguyen, Thy L. T. Ho, Bin Wang
article en

Abstract

Hydrogen production from biomass and natural gas has emerged as a prominent research area in response to the growing demand for energy from alternative sources that minimize CO<sub>2</sub> emissions. In this study, we investigate the impact of water, which is present in and generated from biomass-derived streams, on carbon nanotube (CNT) growth and hydrogen production during methane decomposition using Ni-Mo/MgO as a catalyst. We reveal here that the role of water on CNT growth is highly complex; its effect depends on the stage of growth at which the water is incorporated. When water is introduced at the beginning of methane decomposition (<i>t</i> = 0 h), methane conversion rates are negatively impacted. We hypothesize that water inhibits the significant phase changes the Ni-Mo/MgO catalyst undergoes during catalyst carburization. In contrast, the incorporation of a small percentage of water after a stabilization period (<i>t</i> = 3 h) results in methane conversion rate enhancements that scale with the introduced water partial pressure as water selectively reacts with amorphous carbon deposits that lead to catalyst deactivation, thus prolonging the lifetime of some of the most active sites. Moreover, water incorporation after stabilization significantly reduces the apparent activation energy. Density Functional Theory (DFT) calculations reveal that water preferentially interacts with carbon fragments on the catalyst surface to remove carbon deposits with a barrier lower than that required for methane activation, further supporting its role in cleaning active sites on the catalyst surface. Characterization of the resulting carbon nanotubes reveals the formation of more graphitic materials produced in the presence of water, highlighting the impact of water on nanotube properties. These results provide clarity toward the many ways in which water, or cofeeding of biomass-derived materials, may impact catalytic methane pyrolysis rates.

ACS CatalysisVol. 16(6)
Sustainable Energy Systems (United Kingdom) (GB), University of Oklahoma (US)
Openalex Percentile: Top 42%
Catalysts for Methane Reforming
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