Cobalt catalyst used for catalyzing o-methoxy-phenol to prepare cyclohexanol and preparation method of cobalt catalyst
A technology of o-methoxyphenol and catalyst, applied in the field of metal cobalt catalyst and preparation thereof, can solve the problems of improvement, unfavorable economic benefits, etc., and achieves the advantages of improved dispersibility and reducibility, improved hydrodeoxygenation activity, and improved selectivity. Effect
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Embodiment 1
[0025] 14.8g Co(NO 3 ) 2 ·6H 2 O, 4.0g ZrOCl 2 ·8H 2 O and 2.7g Ce(NO 3 ) 3 ·6H 2 O was dissolved in 100ml of deionized water and stirred to form a mixed solution of metal salts. Add 9.2g of anhydrous Na 2 CO 3 Dissolve in 100ml deionized water and stir to form Na 2 CO 3 Solution, the above two solutions were slowly added dropwise to 200ml of deionized water at the same time in a water bath at 50°C and stirred vigorously for 1 hour to form a purple precipitate. The pH value of the filtrate obtained after suction filtration is 8-9, the precipitate is washed thoroughly with deionized water until the filtrate is neutral, and the precipitate is added to 200 ml of n-butanol. Evaporate in a water bath at 50°C for 12h, and then dry it in an oven at 80°C for 12h to obtain the catalyst precursor, press and grind it to sieve out 20-40 mesh particles, pass hydrogen into a fixed bed, and reduce at 450°C for 3~ 5h, get the hydrogenation catalyst.
[0026] In a fixed-bed reactor, add 0.2g of c...
Embodiment 2
[0028] Take 2.3g ZrOCl 2 ·8H 2 O and 4.7g Ce(NO 3 ) 3 ·6H 2 O instead of 4.0g ZrOCl in Example 1 2 ·8H 2 O and 2.7g Ce(NO 3 ) 3 ·6H 2 O, the other steps are the same as in Example 1.
Embodiment 3
[0030] Take 2.8g ZrOCl 2 ·8H 2 O and 3.8g Ce(NO 3 ) 3 ·6H 2 O instead of 4.0g ZrOCl in Example 1 2 ·8H 2 O and 2.7g Ce(NO 3 ) 3 ·6H 2 O, the other steps are the same as in Example 1.
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