Catalyst for producing vinyl acetate by ethylene process
A method of vinyl acetate and catalyst technology, which is applied in physical/chemical process catalysts, organic compound/hydride/coordination complex catalysts, organic chemistry, etc., can solve the problems of low activity and selectivity of vinyl acetate catalysts, and achieve improvement Effects of activity and stability, yield enhancement and selectivity
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Embodiment 1
[0034] Catalyst preparation:
[0035] (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;
[0036] (2) After drying at 80°C, 98ml contains 20.5g Na 2 SiO 3 9H 2 The solution of O is fully mixed, and aging 24h obtains catalyst precursor II;
[0037] (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;
[0038] (4) Lanthanum acetate (La(OA) containing 1.48gLa 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 pre...
Embodiment 2
[0045] Catalyst preparation:
[0046] (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;
[0047] (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;
[0048] (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;
[0049] (4) Immerse 150ml of bismuth ammonium citrate aqueous solution containing 1.48gBi on the precursor III, vacuum dry at 110°C, and roast at 400°C to obtain the catalyst precursor IV;
[0050] (5) Dissolve...
Embodiment 3
[0068] Catalyst preparation:
[0069] (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;
[0070] (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;
[0071] (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;
[0072] (4) Cerium acetate containing 1.48gCe (Ce(OA 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...
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