کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6455040 1418819 2017 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Layered double hydroxides derived Nix(MgyAlzOn) catalysts: Enhanced ammonia decomposition by hydrogen spillover effect
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Layered double hydroxides derived Nix(MgyAlzOn) catalysts: Enhanced ammonia decomposition by hydrogen spillover effect
چکیده انگلیسی


- NiMgAl-layered double hydroxides derived Ni catalysts for NH3 decomposition.
- Catalyst of certain constitution showed high efficiency and excellent durability.
- Superior performance is associated with the Mg site synergism toward Ni.
- “Spillover effect” of surface hydrogen accounts for a higher turnover frequency.

The NiMgAl-layered double hydroxides, with the stoichiometric ratios of Mg/Ni and Mg/Al being 0-9 and 0-3, respectively, were synthesized and employed as the Ni catalyst precursors for NH3 decomposition. The resulting catalyst of the certain Ni, Mg, and Al contents showed high catalytic efficiency and outstanding durability for the target reaction. The features of cost effective (with only Mg and Al elements besides Ni), easy fabrication, and thermally durable are attractive for large-scale operation. The characterizations revealed the related changes in structure and property, such as the Ni particle size and distribution, the reduction of Ni2+ species, the Ni-oxide matrix interaction, the surface basicity as well as the adsorption/desorption behavior of hydrogen, in line with the stoichiometry of Ni, Mg, and Al in the samples. The superior catalytic activity and stability are thought to be associated with the structurally isolated active Ni species by the oxide matrix and the synergism between Ni-Mg sites. Particularly, the “spillover effect” of surface hydrogen accounts for a higher turnover frequency.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Applied Catalysis B: Environmental - Volume 201, February 2017, Pages 451-460
نویسندگان
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