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author:

Xu, Y. (Xu, Y..) [1] | Yao, J. (Yao, J..) [2] | Lin, H. (Lin, H..) [3] | Lv, Q. (Lv, Q..) [4] | Liu, B. (Liu, B..) [5] | Wu, L. (Wu, L..) [6] (Scholars:吴立志) | Tan, L. (Tan, L..) [7] (Scholars:谭理) | Dai, Y. (Dai, Y..) [8] | Zong, X. (Zong, X..) [9] | Tang, Y. (Tang, Y..) [10] (Scholars:汤禹)

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Scopus

Abstract:

Enhancing catalyst durability is a critical concern in the partial oxidation of methane (POM) to syngas since the reaction is operated at high temperatures (>600 °C). Alongside sintering and coke deposition, the deactivation of the supported Ni catalyst is often due to the in situ oxidation of active metallic nanoparticles into inactive cations during the POM reaction. Herein, a Ni/BN catalyst was developed by introducing functional CeOx as a promoter to stabilize the Ni sites. The optimized 4Ni/7.5Ce/BN catalyst, comprising 4 wt % Ni and 7.5 wt % Ce on BN, exhibits enhanced stability during continuous testing at 600 °C for 125 h without any deactivation, which is comparable to that of noble metal catalysts. Comprehensive investigations reveal that maintaining the metallic state of Ni under reaction atmosphere is crucial for the stability of the catalyst. The construction of CeOx on BN effectively inhibits migration and oxidation of the catalytically active Ni0 species. © 2024 American Chemical Society.

Keyword:

boron nitride catalyst deactivation ceria methane reforming nickel partial oxidation of methane strong metal support interaction syngas

Community:

  • [ 1 ] [Xu Y.]Institute of Molecular Engineering Plus, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 2 ] [Yao J.]Institute of Molecular Engineering Plus, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 3 ] [Lin H.]Institute of Molecular Engineering Plus, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 4 ] [Lv Q.]Institute of Molecular Engineering Plus, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 5 ] [Liu B.]Institute of Molecular Engineering Plus, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 6 ] [Wu L.]Institute of Molecular Engineering Plus, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 7 ] [Tan L.]Institute of Molecular Engineering Plus, College of Chemistry, Fuzhou University, Fuzhou, 350108, China
  • [ 8 ] [Dai Y.]Institute of Advanced Synthesis, School of Chemistry and Molecular Engineering, Nanjing Tech University, Nanjing, 211816, China
  • [ 9 ] [Zong X.]Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China
  • [ 10 ] [Tang Y.]Institute of Molecular Engineering Plus, College of Chemistry, Fuzhou University, Fuzhou, 350108, China

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Source :

ACS Catalysis

ISSN: 2155-5435

Year: 2024

Issue: 15

Volume: 14

Page: 11845-11856

1 1 . 7 0 0

JCR@2023

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 1

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