High-load metal nickel catalyst as well as preparation method and application thereof
A metal nickel and catalyst technology, applied in the field of catalysis, can solve the problems of affecting the hydrodeoxygenation activity of the catalyst, difficult to prepare a high-loaded metal nickel catalyst, etc., and achieve the effects of overcoming unstable crystal phase, overcoming poor texture, and promoting dispersion.
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Embodiment 1
[0030] (1) 29.7g Ni(NO 3 ) 2 ·6H 2 O, 23g TiCl 4 - Ethanol (0.3g / g) solution dissolved in 100ml deionized water to form nickel nitrate and TiCl 4 - mixed solution of ethanol;
[0031] (2) 5.2g Na 2 SiO 3 9H 2 O and 18.2 g anhydrous Na 2 CO 3 Dissolve in 100ml deionized water to form Na 2 SiO 3 9H 2 O and Na 2 CO 3 mixed solution;
[0032] (3) The above two mixed solutions were slowly added dropwise to 200ml deionized water at the same time in a water bath at 80°C, and stirred vigorously for 1 hour to form a green precipitate. The pH value of the filtrate obtained after suction filtration is 8-9, and the precipitate is fully washed with deionized water until the filtrate is neutral and the chloride ions in the solution are thoroughly washed away, and the precipitate is added to 200 ml of n-butanol. Evaporate in a water bath at 80°C for 12 hours, then dry in an oven at 120°C for 12 hours to obtain the precursor of the catalyst;
[0033] (4) Place the precursor in...
Embodiment 2
[0035] (1) 29.7g Ni(NO 3 ) 2 ·6H 2 O, 18.1g TiCl 4 - Ethanol (0.3g / g) solution dissolved in 100ml deionized water to form nickel nitrate and TiCl 4 - mixed solution of ethanol;
[0036] (2) 8.1g Na 2 SiO 3 9H 2 O and 15.3 g anhydrous Na 2 CO 3 Dissolve in 100ml deionized water to form Na 2 SiO 3 9H 2 O and Na 2 CO 3 mixed solution;
[0037] (3) The above two solutions were slowly added dropwise to 200ml deionized water at the same time in a water bath at 80°C, and stirred vigorously for 1 hour to form a green precipitate. The pH value of the filtrate obtained after suction filtration is 8-9, and the precipitate is fully washed with deionized water until the filtrate is neutral and the chloride ions in the solution are thoroughly washed away, and the precipitate is added to 200 ml of n-butanol. Evaporate in a water bath at 80°C for 12 hours, then dry in an oven at 120°C for 12 hours to obtain the precursor of the catalyst;
[0038] (4) Place the precursor in a t...
Embodiment 3
[0040] (1) 29.7g Ni(NO 3 ) 2 ·6H 2 O, 13g TiCl 4 - Ethanol (0.3g / g) solution dissolved in 100ml deionized water to form nickel nitrate and TiCl 4 - mixed solution of ethanol;
[0041] (2) 11.4g Na 2 SiO 3 9H 2 O and 11.9 g anhydrous Na 2 CO 3 Dissolve in 100ml deionized water to form Na 2 SiO 3 9H 2 O and Na 2 CO 3 mixed solution;
[0042] (3) The above two solutions were slowly added dropwise to 200ml deionized water at the same time in a water bath at 80°C, and stirred vigorously for 1 hour to form a green precipitate. The pH value of the filtrate obtained after suction filtration is 8-9, and the precipitate is fully washed with deionized water until the filtrate is neutral and the chloride ions in the solution are thoroughly washed away, and the precipitate is added to 200 ml of n-butanol. Evaporate in a water bath at 80°C for 12 hours, then dry in an oven at 120°C for 12 hours to obtain the precursor of the catalyst;
[0043] (4) Place the precursor in a tu...
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