Catalyst for preparing synthetic gas by reforming of methane and carbon dioxide as well as preparation method and application of catalyst
A carbon dioxide and catalyst technology, applied in the field of catalyst preparation, can solve the problems of high catalyst cost, complicated preparation process, easy carbon deposition and deactivation, etc., and achieve the effects of high selectivity, good catalytic performance and developed pores
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Embodiment 1
[0035] (1) Preparation of activated carbon:
[0036]Oxidize 30g lignite in the air at 70°C, wash, dry, and pulverize, and sieve into 250-mesh carbon powder (A); wash and dry 45g corn cobs, vacuum carbonize at 230°C, pulverize, and sieve into 250-mesh carbon powder Powder (B); mix (A) and (B) at 40%:60%, then soak in 1.25mol / L potassium carbonate solution for 10h, suction filter and dry to get (C). (C) was activated by heating charcoal in a tube furnace under nitrogen and oxygen barrier conditions, the charcoal activation temperature was 500°C, the heating rate was 10°C / min, and the activation time was 2h. Then it was washed with distilled water until the pH was 7.5, and dried at 100° C. for 10 h to obtain 27.75 g of activated carbon.
[0037] (2) Preparation of supported catalyst:
[0038] Weigh 20g of activated carbon, and ultrasonically impregnate it in a solution of 1.05mol / L cobalt nitrate hexahydrate, 0.15mol / L zirconium nitrate pentahydrate and 0.03mol / L ammonium hepta...
Embodiment 2
[0043] (1) Preparation of activated carbon:
[0044] Oxidize 30g lignite in the air at 70°C, wash, dry, and pulverize, and sieve into 250 mesh carbon powder (A); wash and dry 75g corncobs, vacuum carbonize at 230°C, pulverize, and sieve into 250 mesh Powder (B); mix (A) and (B) at 28.5%: 71.5%, then soak in 1.27mol / L potassium carbonate solution for 10h, filter with suction and dry to get (C). (C) was activated by heating charcoal in a tube furnace under nitrogen and oxygen barrier conditions, the charcoal activation temperature was 500°C, the heating rate was 10°C / min, and the activation time was 2h. Then it was washed with distilled water until the pH was 7.5, and dried at 100° C. for 10 h to obtain 33.2 g of activated carbon.
[0045] (2) Preparation of supported catalyst:
[0046] Weigh 20g of activated carbon, and ultrasonically impregnate it in a solution of 1.12mol / L cobalt nitrate hexahydrate, 0.15mol / L zirconium nitrate pentahydrate and 0.03 mol / L ammonium heptamoly...
Embodiment 3
[0051] (1) Preparation of activated carbon:
[0052] Oxidize 30g lignite in the air at 70°C, wash, dry, and crush, and sieve into 250 mesh carbon powder (A); wash and dry 110g corncobs, vacuum carbonize at 230°C, crush, and sieve into 250 mesh Powder (B); mix (A) and (B) at a ratio of 22%: 78%, then soak in 1.30mol / L potassium carbonate solution for 10h, filter and dry to obtain (C). (C) was activated by heating charcoal in a tube furnace under nitrogen and oxygen barrier conditions, the charcoal activation temperature was 500°C, the heating rate was 10°C / min, and the activation time was 2h. Then it was washed with distilled water until the pH was 7.5, and dried at 100° C. for 10 h to obtain 43.5 g of activated carbon.
[0053] (2) Preparation of supported catalyst:
[0054] Weigh 20g of activated carbon, and ultrasonically impregnate it in a solution of 1.20mol / L cobalt nitrate hexahydrate, 0.15mol / L zirconium nitrate pentahydrate and 0.03 mol / L ammonium heptamolybdate tetr...
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