Minhazur Rahman Shawon, Chinwendu Umeojiakor, Anthony Griffin, Jeffrey Aguinaga, Jiachun Wu, Derek Patton, Zhe Qiang, Hossein Toghiani and Yizhi Xiang
{"title":"Ammonia decomposition over low-loading ruthenium catalyst achieved through “adiabatic” plasma reactor†","authors":"Minhazur Rahman Shawon, Chinwendu Umeojiakor, Anthony Griffin, Jeffrey Aguinaga, Jiachun Wu, Derek Patton, Zhe Qiang, Hossein Toghiani and Yizhi Xiang","doi":"10.1039/D4RE00509K","DOIUrl":null,"url":null,"abstract":"<p >Electrified catalytic processes for ammonia (NH<small><sub>3</sub></small>) decomposition have been considered as essential technologies for distributed CO<small><sub><em>x</em></sub></small>-free hydrogen production. Here we show that efficient NH<small><sub>3</sub></small> decomposition can be achieved over low-loading Ru/Al<small><sub>2</sub></small>O<small><sub>3</sub></small> using an adiabatic dielectric barrier discharge (DBD) plasma reactor. Specifically, we demonstrate that the activity of NH<small><sub>3</sub></small> decomposition in the adiabatic plasma reactor is up to 4.9 times higher than that under nonadiabatic conditions. The NH<small><sub>3</sub></small> conversion was 73% (in the adiabatic plasma reactor) over the 0.05 wt% Ru/Al<small><sub>2</sub></small>O<small><sub>3</sub></small> catalysts at a plasma power of 19 W, whereas, the conversion is only 15% when performed in the nonadiabatic plasma reactor, moreover, the catalyst was almost inactive in the thermal catalytic NH<small><sub>3</sub></small> decomposition. Additionally, nearly 100% NH<small><sub>3</sub></small> conversion was achieved over the 0.5 wt% Ru/Al<small><sub>2</sub></small>O<small><sub>3</sub></small> catalyst at 19 W or over higher Ru loading catalysts at lower powers. We suggested that more efficient NH<small><sub>3</sub></small> decomposition was attributed to the enhanced synergy between plasma-activated radicals ·NH<small><sub><em>x</em></sub></small> and vibrationally excited NH<small><sup>v</sup></small><small><sub>3</sub></small>, and the catalytically active Ru sites when using the adiabatic plasma reactor – in contrast to the nonadiabatic counterpart.</p>","PeriodicalId":101,"journal":{"name":"Reaction Chemistry & Engineering","volume":" 2","pages":" 320-331"},"PeriodicalIF":3.4000,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reaction Chemistry & Engineering","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/re/d4re00509k","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Electrified catalytic processes for ammonia (NH3) decomposition have been considered as essential technologies for distributed COx-free hydrogen production. Here we show that efficient NH3 decomposition can be achieved over low-loading Ru/Al2O3 using an adiabatic dielectric barrier discharge (DBD) plasma reactor. Specifically, we demonstrate that the activity of NH3 decomposition in the adiabatic plasma reactor is up to 4.9 times higher than that under nonadiabatic conditions. The NH3 conversion was 73% (in the adiabatic plasma reactor) over the 0.05 wt% Ru/Al2O3 catalysts at a plasma power of 19 W, whereas, the conversion is only 15% when performed in the nonadiabatic plasma reactor, moreover, the catalyst was almost inactive in the thermal catalytic NH3 decomposition. Additionally, nearly 100% NH3 conversion was achieved over the 0.5 wt% Ru/Al2O3 catalyst at 19 W or over higher Ru loading catalysts at lower powers. We suggested that more efficient NH3 decomposition was attributed to the enhanced synergy between plasma-activated radicals ·NHx and vibrationally excited NHv3, and the catalytically active Ru sites when using the adiabatic plasma reactor – in contrast to the nonadiabatic counterpart.
期刊介绍:
Reaction Chemistry & Engineering is a new journal reporting cutting edge research into all aspects of making molecules for the benefit of fundamental research, applied processes and wider society.
From fundamental, molecular-level chemistry to large scale chemical production, Reaction Chemistry & Engineering brings together communities of chemists and chemical engineers working to ensure the crucial role of reaction chemistry in today’s world.