Loaded complex catalyst for isobutylene hydrogen formylation reaction
A technology of isobutylene hydroformyl and catalyst, which is applied in the direction of organic compound/hydride/coordination complex catalyst, physical/chemical process catalyst, hydrogenation hydrocarbon production, etc., and can solve the problems of popularization and application, complex preparation process, and catalyst activity group. Distributor loss and other issues
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example 1
[0011] (1) Catalyst preparation
[0012] Weigh 0.253g Co(NO 3 ) 2 ·6H 2 O, dissolved in distilled water, added 2.928g of SiO 2 The carrier was impregnated for 45min, then evaporated to dryness in a water bath at 80°C, dried in an oven at 120°C for 24h, and calcined in a tube furnace at 400°C for 3h under nitrogen protection. The obtained solid was impregnated with an acetone solution containing 0.124 g of triphenylphosphine for 30 min under the protection of nitrogen in a rotary evaporator, and then dried in vacuo to remove the acetone to obtain a supported cobalt-based complex catalyst, labeled as COSi-TPP; in an inert atmosphere Store for later use.
[0013] (2) Investigation of the activity of the catalyst
[0014] The hydroformylation reaction of isobutene was carried out in a 250ml magnetically driven stirred autoclave. Add 80ml of solvent xylene and 1.0g of catalyst to the reaction kettle, close the autoclave, replace the air in the system with nitrogen three times...
example 2
[0017] Weigh 0.073g RhCl 3 ·3H 2 O and 2.964g SiO 2 , the concrete steps are prepared with the catalyst in the reference example one, and the activity investigation of the catalyst is the same as the reference example one. The results showed that the conversion rate of isobutene was 44.66%, and the selectivity of isovaleraldehyde was 77.43%.
Embodiment 1
[0019] Weigh 0.073g RhCl 3 ·3H 2 O, 0.253g Co(NO 3 ) 2 ·6H 2 O and 2.892g SiO 2 , the concrete steps are prepared with the catalyst in the reference example one, and the activity investigation of the catalyst is the same as the reference example one. The results showed that the conversion rate of isobutene was 62.0%, and the selectivity of isovaleraldehyde was 89.3%.
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