Catalysts used in the synthesis of ethylene vinyl acetate
A method of vinyl acetate and catalyst technology, applied in the direction of organic compound/hydride/coordination complex catalyst, physical/chemical process catalyst, organic compound preparation, etc., can solve the problem of low activity and selectivity of vinyl acetate catalyst, Achieve the effect of improving activity and stability, improving yield and selectivity
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Embodiment 1
[0036] Catalyst preparation:
[0037] (1) Using sodium bicarbonate pH regulator and water as a solvent to prepare a pH of 1.09, containing 3.85gPd and 1.87gAu of chloropalladic acid and chloroauric acid aqueous solution to obtain 500ml of impregnation solution, which is impregnated on the carrier in a rotating pot 1.0L of spherical SiO with a diameter of 5.6mm 2 Catalyst precursor I is obtained on the carrier;
[0038] (2) After drying at 80°C, 98ml contains 20.5g Na 2 SiO 3 9H2 The solution of O is fully mixed, aged for 24h to obtain catalyst precursor II;
[0039] (3) With a solubility of 12% (in N 2 h 4 ·H 2 (2 in weight ratio) is reduced by 500ml hydrazine hydrate, washed with water to no chloride ion, and dried at 90° C. to obtain catalyst precursor III;
[0040] (4) Samarium acetate (Sm(OA) containing 1.39gSm C ) 3 ·6H 2 O) 150ml of the aqueous solution is impregnated on the precursor III, vacuum-dried at 110°C, and calcined at 400°C to obtain the catalyst prec...
Embodiment 2
[0047] Catalyst preparation:
[0048] (1) Using sodium bicarbonate pH regulator and water as a solvent to prepare a pH of 1.09, containing 3.85gPd and 1.87gAu of chloropalladic acid and chloroauric acid aqueous solution to obtain 500ml of impregnation solution, which is impregnated on the carrier in a rotating pot 1.0L of spherical SiO with a diameter of 5.6mm 2 Catalyst precursor I is obtained on the carrier;
[0049] (2) After drying at 80°C, 98ml contains 20.5g Na 2 SiO 3 9H 2 The solution of O is fully mixed, aged for 24h to obtain catalyst precursor II;
[0050] (3) With a solubility of 12% (in N 2 h 4 ·H 2 (2 in weight ratio) is reduced by 500ml hydrazine hydrate, washed with water to no chloride ion, and dried at 90° C. to obtain catalyst precursor III;
[0051] (4) Cadmium acetate containing 1.39gCd (Cd(OA C ) 2 2H 2 O) 150ml of the aqueous solution is impregnated on the precursor III, vacuum-dried at 110°C, and calcined at 400°C to obtain the catalyst precu...
Embodiment 3
[0070] Catalyst preparation:
[0071] (1) Using sodium bicarbonate pH regulator and water as a solvent to prepare a pH of 1.09, containing 3.85gPd and 1.87gAu of chloropalladic acid and chloroauric acid aqueous solution to obtain 500ml of impregnation solution, which is impregnated on the carrier in a rotating pot 1.0L spherical Al with a diameter of 5.6mm 2 o 3 Catalyst precursor I is obtained on the carrier;
[0072] (2) After drying at 80°C, 98ml contains 20.5g Na 2 SiO 3 9H 2 The solution of O is fully mixed, aged for 24h to obtain catalyst precursor II;
[0073] (3) With a solubility of 12% (in N 2 h 4 ·H 2 (2 in weight ratio) is reduced by 500ml hydrazine hydrate, washed with water to no chloride ion, and dried at 90° C. to obtain catalyst precursor III;
[0074] (4) Lanthanum acetate (La(OA) containing 1.39gLa C ) 3 ·5H 2 O) 150ml of the aqueous solution is impregnated on the precursor III, vacuum-dried at 110°C, and calcined at 400°C to obtain the catalyst ...
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