Enhanced N2O capture and reduction system using Cu/zeolite adsorbent and Pd/La/Al2O3 catalyst under O2-CO2-rich conditions

  • Chenxi He
  • , Leyang Zhang
  • , Jörg W.A. Fischer
  • , Jialei Zhang
  • , Shinta Miyazaki
  • , Ningqiang Zhang
  • , Junxian Qin
  • , Akihiko Anzai
  • , Ken-ichi Shimizu
  • , Takashi Toyao

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Nitrous oxide (N2O) is a potent greenhouse gas associated with increasing environmental risks, particularly due to its global warming potential. The removal of N2O remains challenging because catalytic decomposition typically requires high temperatures, especially in the presence of co-existing gases such as O2 and CO2. In this study, we explored various adsorbents that are efficient for N2O adsorption in the presence of O2 and CO2 and found that a CHA-type zeolite loaded with 10 wt% Cu (Cu(10)/CHA) was particularly effective. We developed a two-step N2O capture and reduction system using the Cu(10)/CHA adsorbent and Pd nanoparticles loaded on La-doped Al2O3 (Pd/La/Al2O3) as a catalyst. This system maintained its N2O adsorption and reduction capability for at least 12 h (9 cycles) while operating continuously over a temperature swing of 50–150 °C.

Original languageEnglish
Article number125883
JournalApplied Catalysis B: Environment and Energy
Volume382
DOIs
Publication statusPublished - Mar 2026
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2025 Elsevier B.V.

Funding

This study was financially supported by KAKENHI (Grant No. 21H04626, 23K26690, and 23K20034) from the Japan Society for the Promotion of Science (JSPS) and the Japanese Ministry of Education, Culture, Sports, Science, and Technology (MEXT) within the project “Integrated Research Consortium on Chemical Sciences (IRCCS).” J. W. A. F. gratefully acknowledges the support from the JSPS Postdoctoral Fellowship (PE24052). The authors are greatful to Dr. Hiroshi Hirata, Hokkaido University, for his assistance at the EPR facility. Additional data can be found in the supporting information. This study was financially supported by KAKENHI (Grant No. 21H04626 , 23K26690 , and 23K20034 ) from the Japan Society for the Promotion of Science ( JSPS ) and the Japanese Ministry of Education, Culture, Sports, Science, and Technology ( MEXT ) within the project “Integrated Research Consortium on Chemical Sciences ( IRCCS ).” J. W. A. F. gratefully acknowledges the support from the JSPS Postdoctoral Fellowship (PE24052). The authors are greatful to Dr. Hiroshi Hirata, Hokkaido University, for his assistance at the EPR facility.

FundersFunder number
Japan Society for the Promotion of Science
Ministry of Education, Culture, Sports, Science and TechnologyPE24052

    Keywords

    • Continuous capture and reduction
    • Cu/zeolite
    • Greenhouse gas
    • N O removal

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