Catalyst for production of ethylene method vinyl acetate
A method of vinyl acetate and catalyst technology, which is applied in the direction of physical/chemical process catalysts, carboxylate preparation, metal/metal oxide/metal hydroxide catalysts, etc., and can solve the problems of low activity and selectivity of vinyl acetate catalysts, Achieve the effect of improving activity and stability, improving yield and selectivity
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[0030] [Example 1]
[0031] Preparation of catalyst:
[0032] (1) with sodium bicarbonate pH value regulator and water as solvent preparation pH is 1.09, containing the chloropalladium acid of 3.85gPd and 1.87gAu, chloroauric acid aqueous solution, obtain dipping solution 500ml, in the rotating pot, it is dipped in the carrier 1.0L spherical SiO with a diameter of 5.6mm 2 Catalyst precursor I is obtained on the carrier;
[0033] (2) After drying at 80°C, 98ml contains 20.5g Na 2 SiO 3 ·9H 2 The solution of O was fully mixed and aged for 24h to obtain catalyst precursor II;
[0034] (3) with a solubility of 12% (in N 2 H 4 ·H 2 (0 weight ratio) is 500ml of hydrazine hydrate for reduction, washed with water until there is no chloride ion, and dried at 90 ° C to obtain catalyst precursor III;
[0035] (4) Cobalt acetate (Co(OA) containing 1.27g CoC ) 2 ·4H 2 O) 150ml of aqueous solution was impregnated on precursor III, vacuum-dried at 110°C, and calcined at 400°C to o...
Example Embodiment
[0041] [Example 2]
[0042] Preparation of catalyst:
[0043] (1) with sodium bicarbonate pH value regulator and water as solvent preparation pH is 1.09, containing the chloropalladium acid of 3.85gPd and 1.87gAu, chloroauric acid aqueous solution, obtain dipping solution 500ml, in the rotating pot, it is dipped in the carrier 1.0L spherical SiO with a diameter of 5.6mm 2 Catalyst precursor I is obtained on the carrier;
[0044] (2) After drying at 80°C, 98ml contains 20.5g Na 2 SiO 3 ·9H 2 The solution of O was fully mixed and aged for 24h to obtain catalyst precursor II;
[0045] (3) with a solubility of 12% (in N 2 H 4 ·H 2 (0 weight ratio) is 500ml of hydrazine hydrate for reduction, washed with water until there is no chloride ion, and dried at 90 ° C to obtain catalyst precursor III;
[0046] (4) stannous chloride (SnCl) containing 1.27g Sn 2 ·2H 2 O) 150ml of aqueous solution was impregnated on precursor III, vacuum-dried at 110°C, and calcined at 400°C to ob...
Example Embodiment
[0064] [Example 3]
[0065] Preparation of catalyst:
[0066] (1) with sodium bicarbonate pH value regulator and water as solvent preparation pH is 1.09, containing the chloropalladium acid of 3.85gPd and 1.87gAu, chloroauric acid aqueous solution, obtain dipping solution 500ml, in the rotating pot, it is dipped in the carrier 1.0L spherical Al with a diameter of 5.6mm 2 O 3 Catalyst precursor I is obtained on the carrier;
[0067] (2) After drying at 80°C, 98ml contains 20.5g Na 2 SiO 3 ·9H 2 The solution of O was fully mixed and aged for 24h to obtain catalyst precursor II;
[0068] (3) with a solubility of 12% (in N 2 H 4 ·H 2 (0 weight ratio) is 500ml of hydrazine hydrate for reduction, washed with water until there is no chloride ion, and dried at 90 ° C to obtain catalyst precursor III;
[0069] (4) Cobalt nitrate (Co(NO) containing 1.27g Co 3 ) 2 ·6H 2 O) 150ml of aqueous solution was impregnated on precursor III, vacuum-dried at 110°C, and calcined at 400°...
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