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  • 教师姓名: 吴小梅
  • 性别: 女
  • 职称: 副教授
  • 博士生导师: 是
  • 硕士生导师: 是
  • 学历: 博士研究生毕业
  • 学位: 博士
  • 所在单位: 化学工程与技术学院
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  • 办公地点: 创新港19-4F045
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论文成果

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Taming NO oxidation efficiency by gamma-MnO(2)morphology regulation

发布时间:2025-11-23
点击次数:
发布时间:
2025-11-23
影响因子:
5.721
DOI码:
10.1039/d0cy00573h
论文名称:
Taming NO oxidation efficiency by gamma-MnO(2)morphology regulation
发表刊物:
CATALYSIS SCIENCE & TECHNOLOGY
关键字:
SELECTIVE CATALYTIC-REDUCTION;NITRIC-OXIDE;MANGANESE OXIDES;FACILE SYNTHESIS;MNO2;SURFACE;PERFORMANCE;REMOVAL;MECHANISM;MORPHOLOGIES
摘要:
Nitric oxide (NO) emitted from the combustion of fossil fuels has drawn global concern, and the oxidation of NO contributes greatly to the DeNO(x)process. Herein, single-crystal gamma-MnO(2)catalysts with well-defined hollow-sphere-, sea-urchin-, and flower-like morphologies (gamma-MnO2-HS, gamma-MnO2-SU, and gamma-MnO2-F) were rationally designed and synthesizedviaan environmental-friendly template-free hydrothermal strategy. The physicochemical properties of the prepared materials were characterized by XRD, FE-SEM, TEM, BET, XPS, H-2-TPR, O-2/NO-TPD andin situDRIFTS, and their catalytic activities in NO oxidation were evaluated. The results showed the gamma-MnO2-HS sample possessed the highest activity and could oxidize 91.1% of NO at 275 degrees C, which was obviously higher than those of the gamma-MnO2-SU and gamma-MnO2-F catalysts. It was found that the presence of abundant surface-adsorbed oxygen and the largest quantity of Mn(3+)over the gamma-MnO2-HS material respectively accelerated the processes of NO adsorption and O(2)activation, which greatly promoted the NO oxidation process. This work provides significant insights into NO oxidation over gamma-MnO(2)catalysts.
卷号:
10
页面范围:
5996-6005
ISSN号:
2044-4753
是否译文:
发表时间:
2020-01-01
收录刊物:
SCI、SCI