Cu-Co base catalyst
A catalyst, cu-co technology, applied in the field of Cu-Co-based catalysts, can solve problems affecting the composition of reaction products and achieve excellent catalytic performance
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Embodiment 1
[0021] a) Add Cu 2+ 、Co 2+ and K + According to 1:2:3 molar ratio as raw material, Cu 2+ and Co 2+ Prepare solution I by mixing the total concentration of the two ions at 1.0 mol / L, and prepare another solution K + Solution II with a concentration of 2mol / L;
[0022] b) Add solution I and solution II dropwise to a Erlenmeyer flask in a water bath at 70°C at the same time, stir, and react at 70°C for 5 hours;
[0023] c) Vacuum filter the resulting precipitate and wash with water until the K in the precipitate is + Rinse until dry.
[0024] d) put the precipitate obtained in step c) in N 2 Baking at 500°C for 3h under protection.
[0025] e) Press the calcined product into tablets and sieve to 30-40 mesh.
Embodiment 2
[0027] a) Add Cu 2+ 、Co 2+ and K + According to 1:3:3 molar ratio as raw material, Cu 2+ and Co 2+ Solution I was prepared by mixing the total concentration of the two ions at 2.8mol / L, and another solution was prepared as K + Solution II with a concentration of 2.7mol / L;
[0028] b) Add solution I and solution II dropwise to a conical flask in a water bath at 60-90°C at the same time, stir, and react at 80°C for 4 hours;
[0029] c) Vacuum filter the resulting precipitate and wash with water until the K in the precipitate is + Rinse until dry.
[0030] d) put the precipitate obtained in step c) in N 2 Baking at 500°C for 4h under protection.
[0031] e) Press the calcined product into tablets and sieve to 40-50 mesh.
Embodiment 3
[0033] a) Add Cu 2+ 、Co 2+ and K + According to 1:3:5 molar ratio as raw material, Cu 2+ and Co 2+ Solution I was prepared by mixing the total concentration of the two ions at 2.3mol / L, and another solution was prepared as K + Solution II with a concentration of 1.6mol / L;
[0034] b) Add solution I and solution II dropwise into a conical flask in a water bath at 60°C, stir, and react at 60°C for 6 hours;
[0035] c) Vacuum filter the resulting precipitate and wash with water until the K in the precipitate is + Rinse until dry.
[0036] d) put the precipitate obtained in step c) in N 2 Baking at 500°C for 5h under protection.
[0037] e) Press the calcined product into tablets and sieve to 60-70 mesh.
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