2018
DOI: 10.1007/s11426-018-9261-5
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Promoted porous Co3O4-Al2O3 catalysts for ammonia decomposition

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Cited by 44 publications
(21 citation statements)
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“…Much effort s have been devoted in the development of active catalysts for ammonia decomposition, including both noble metals [ 4,7 −9 ] and transition metals [5,[10][11][12][13][14][15][16][17][18][19][20][21] . Among them, Ru-based catalysts showed the best catalytic activity at the temperatures of 300 −550 °C [4,8,9] .…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Much effort s have been devoted in the development of active catalysts for ammonia decomposition, including both noble metals [ 4,7 −9 ] and transition metals [5,[10][11][12][13][14][15][16][17][18][19][20][21] . Among them, Ru-based catalysts showed the best catalytic activity at the temperatures of 300 −550 °C [4,8,9] .…”
Section: Introductionmentioning
confidence: 99%
“…Rational design of transition metal-based catalyst with enhanced catalytic performance at low temperatures is in great significance. Many attempts including using various promoters [ 22 −24 ], designing bimetallic catalysts [25][26][27][28] , choosing proper supports [13,18] and optimizing catalyst preparations [14,16,18] have been studied. It has been reported that support basicity plays a crucial role in ammonia decomposition and the enhanced support basicity can promote the catalytic performance of catalysts [4] .…”
Section: Introductionmentioning
confidence: 99%
“…325 In the work of Zhang et al the conversion of ammonia using Co 3 O 4 reaches its maximum at a reaction temperature of 500 °C, while at higher temperatures the conversion decreases. 325 Czekajło and Lendzion-Bieluń3 26 were able to increase the conversion by adding the oxides of Al, Ca, and K as promoters. The addition of promoter oxides is believed to stabilize the surface area of the catalysts.…”
mentioning
confidence: 98%
“…reaction path and have the same active sites in the ammonia decomposition. Notably, the E a in this work was lower than those of many cobalt‐based catalysts documented in some literature (Table S2), [ 21,42‐43,51 ] which may also be an essential reason for the excellent activity of the Co 0.7 Sm 0.3 O x catalyst.…”
Section: Resultsmentioning
confidence: 58%
“…Besides, the peak around 187 cm –1 was assigned to the tetrahedral sites (CoO 4 ) with F 2 g symmetry. [ 51 ] Moreover, the peak intensity of the different Co a Sm b O x catalysts increased with the increase of cobalt contents.…”
Section: Resultsmentioning
confidence: 99%