Prepn of nickel-base catalyst
A technology of nickel-based catalysts and nickel nitrate, which is applied in chemical instruments and methods, physical/chemical process catalysts, metal/metal oxides/metal hydroxide catalysts, etc., can solve problems such as easy loss and decreased catalytic activity, and achieve Small particle size, large specific surface area, cheap and easy-to-obtain raw materials
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Embodiment 1
[0016] 0.6245 g Ni(NO 3 ) 2 ·6H 2 O was dissolved in 7ml of distilled water to form a nickel nitrate aqueous solution, and then added to a mixed solution formed by 20ml of polyoxyethylene 9-10 octylphenyl ether, 18ml of n-octane and 5ml of n-hexanol. After mixing evenly, add 7 grams of aluminum isopropoxide, stir at 50°C for 3 hours, filter with suction, wash, dry at 80°C, and roast at 600°C for 4 hours in an air atmosphere to obtain the finished catalyst. The particle size of the obtained catalyst was measured to be 8.2nm, and the specific surface area was 357m 2 g -1 .
Embodiment 2
[0018] 2.014 g Ni(NO 3 ) 2 ·6H 2 O was dissolved in 10ml of distilled water to form a nickel nitrate aqueous solution, and then a mixed solution formed of 34ml of polyoxyethylene 9-10 octylphenyl ether, 20ml of n-octane and 15ml of n-hexanol was added. After mixing evenly, add 20ml tetraethyl orthosilicate, stir at 50°C for 2 hours, then filter with suction, wash, dry at 80°C overnight, and then bake at 600°C for 2 hours in an air atmosphere to obtain the finished catalyst. The particle size of the obtained catalyst was measured to be 5.6nm, and the specific surface area was 804m 2 g -1 .
Embodiment 3
[0020] 0.8034 g Ni(NO 3 ) 2 ·6H 2 O was dissolved in 8ml of distilled water, and the preparation process of the catalyst was the same as in Example 1.
[0021] Get this catalyst of 0.4 gram 30-50 mesh and place in the quartz tube reactor of diameter 6mm, pass into 2: 1 methane and oxygen, its space velocity is 8400mlg -1 h -1 , Continuous reaction with temperature programming under normal pressure, the reaction results are listed in Table 1.
[0022] Table 1. Methane conversion and product selectivity of partial oxidation of methane at different temperatures
[0023] temperature x CH4 (%)Y CO (%)Y CO2 (%)Y H2 (%)
[0024] (℃)
[0025] 600 62.3 63.2 36.8 89.8
[0026] 650 74.0 76.7 23.3 94.5
[0027] 700 87.9 89.0 11.0 99.9
[0028] 750 92.3 91.9 8.1 100
[0029] 800 95.8 95.0 5.0 100
[0030] x CH4 :CH 4 Conversion rateY CO : CO selectivity Y CO2 :CO 2 Optional Y H2 :H 2 selectivity
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