Catalyst for synthesis of dimethyl carbonate by using gas-phase method and preparation and application of catalyst
A technology of dimethyl carbonate and catalysts, which is applied in the field of embedded nano-Pd particle catalysts and its preparation, can solve the problems of catalyst activity and service life, chlorine-containing catalysts corrode equipment, etc., and achieve the elimination of equipment corrosion problems and good stability , the effect of high space-time yield
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Embodiment 1
[0025] Add 0.1g sucrose to 10ml deionized water to prepare a solution, and 10g α-Al 2 o 3 The carrier was impregnated in sucrose solution, dried naturally, then placed in an electric blast drying oven, dried at 100°C for 12 hours, and finally dried in N 2 Carbonization at 800°C for 4 hours under atmosphere to obtain a carbonized composite carrier. Dissolve 0.2510g of potassium acetate and 0.3771g of copper acetate in 10ml of deionized water to prepare a mixed solution of auxiliary active component salt. Then 10g of carbonized composite carrier was added into the mixed solution of co-active components, immersed for 8h, dried naturally, dried in a blast oven at 80°C for 12h and baked in a muffle furnace at 400°C for 2h. Add 0.2110g of palladium acetate to 16ml of acetone, and then sonicate in an ultrasonic instrument at 30°C and 20KHz for 30min to prepare a 0.006g Pd / ml solution. Then add the carbonized composite carrier loaded with additives into the main active component so...
Embodiment 2
[0027] Add 0.2g sucrose to 10ml deionized water to prepare a solution, and 10g α-Al 2 o 3 The carrier was impregnated in sucrose solution, dried naturally, then placed in an electric blast drying oven, dried at 100°C for 12 hours, and finally dried in N 2 Carbonization at 800°C for 4 hours under atmosphere to obtain a carbonized composite carrier. Dissolve 0.2510g of potassium acetate and 0.3771g of copper acetate in 10ml of deionized water to prepare a mixed solution of auxiliary active component salt. Then 10g of carbonized composite carrier was added into the mixed solution of co-active components, immersed for 8h, dried naturally, dried in a blast oven at 80°C for 12h and baked in a muffle furnace at 400°C for 2h. Add 0.2110g of palladium acetate to 16ml of acetone, and then sonicate in an ultrasonic instrument at 30°C and 20KHz for 30min to prepare a 0.006g Pd / ml solution. Then add the carbonized composite carrier loaded with additives into the main active component so...
Embodiment 3
[0029] Add 0.4g sucrose to 10ml deionized water to prepare a solution, and 10g α-Al 2 o 3 The carrier was impregnated in sucrose solution, dried naturally, then placed in an electric blast drying oven, dried at 100°C for 12 hours, and finally dried in N 2 Carbonization at 800°C for 4 hours under atmosphere to obtain a carbonized composite carrier. Dissolve 0.2510g of potassium acetate and 0.3771g of copper acetate in 10ml of deionized water to prepare a mixed solution of auxiliary active component salt. Then 10g of carbonized composite carrier was added into the mixed solution of co-active components, immersed for 8h, dried naturally, dried in a blast oven at 80°C for 12h and baked in a muffle furnace at 400°C for 2h. Add 0.2110g of palladium acetate to 16ml of acetone, and then sonicate in an ultrasonic instrument at 30°C and 20KHz for 30min to prepare a 0.006g Pd / ml solution. Then add the carbonized composite carrier loaded with additives into the main active component so...
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