Nano carbon material modified copper base catalyst and its preparing method
A nano-carbon material and copper-based catalyst technology, applied in the chemical industry, can solve the problems that the hydrogen production demand of the vehicle fuel cell cannot be met and the carbon monoxide content in the reformed gas is high.
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Embodiment 1
[0020] Embodiment 1, at first 7.26g Cu (NO 3 ) 2 ·3H 2 O, 8.91g Zn(NO 3 ) 2 ·6H 2 O, 2.50g Al(NO 3 ) 3 9H 2 O (AR grade) was prepared into a 0.1M solution and mixed, and then 7.42g of AR grade anhydrous Na 2 CO 3 Prepared as a 0.1M solution. Then, under strong stirring conditions, the nitrate solution and sodium carbonate solution were dripped into 100mL aqueous solution preset with 0.45g activated carbon powder (400-600 mesh), the solution temperature was controlled at 60°C, and the pH was 7.0-7.2 . Continue to stir for 4 hours after the reaction, then wash with deionized water, fully beat, filter, and finally dry at 110°C for 12h, and bake at 360°C for 4h under the protection of nitrogen to prepare the catalyst precursor in the oxidation state. In the sample, Cu / Zn / Al=45 / 45 / 10 (molar ratio), and the active carbon in the catalyst oxidation state precursor is 8wt%.
[0021] The evaluation of the catalyst's hydrogen production activity by steam reforming of methano...
Embodiment 2
[0025] First, 7.26g Cu(NO 3 ) 2 ·3H 2 O, 8.91g Zn(NO 3 ) 2 ·6H 2 O, 2.50g Al(NO 3 ) 3 9H 2 O (AR grade) was prepared into a 0.1M solution and mixed, and then 7.42g of AR grade anhydrous Na 2 CO 3 Prepared as a 0.1M solution. Then, under the condition of strong stirring, the nitrate solution and the sodium carbonate solution were dripped into the 100mL aqueous solution pre-prepared with 0.45g nano-carbon fiber, the temperature of the solution was controlled at 20°C, and the pH was 7.0-7.2. Continue to stir for 4 hours after the reaction, then wash with deionized water, fully beat, filter, and finally dry at 110°C for 12h, and bake at 360°C for 4h under the protection of nitrogen to prepare the catalyst precursor in the oxidation state. In the sample, Cu / Zn / Al=45 / 45 / 10 (molar ratio), and the carbon nanofiber in the catalyst oxidation state precursor is 8wt%. Catalyst activity evaluation is the same as embodiment 1, and the result shows: at normal pressure, low temper...
Embodiment 3
[0027] First, 7.26g Cu(NO 3 ) 2 ·3H 2 O, 8.91g Zn(NO 3 ) 2 ·6H 2 O, 2.50g Al(NO 3 ) 3 9H 2 O (AR grade) was prepared into a 0.1M solution and mixed, and then 7.42g of AR grade anhydrous Na 2 CO 3 Prepared as a 0.1M solution. Then, under the condition of strong stirring, the nitrate solution and the sodium carbonate solution were dripped into the 100mL aqueous solution pre-placed with 0.45g carbon nanotubes, the temperature of the solution was controlled at 60°C, and the pH was 7.0-7.2. Continue to stir for 4 hours after the reaction, then wash with deionized water, fully beat, filter, and finally dry at 110°C for 12h, and bake at 360°C for 4h under the protection of nitrogen to prepare the catalyst precursor in the oxidation state. In the sample, Cu / Zn / Al=45 / 45 / 10 (mass ratio), and the carbon nanotubes in the catalyst oxidation state precursor are 8wt%. Catalyst activity evaluation is the same as embodiment 1, and the result shows: at normal pressure, low temperatu...
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