Method for preparing active porous carrier supported transition metal salt catalyst
A technology of transition metal salts and transition metals, which is applied in the field of preparation of transition metal salt catalysts, can solve the problems of catalyst difficulty, catalyst activity selectivity decline, separation, etc., and achieve high activity and selectivity effects
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Embodiment 1
[0016] Add 5 g of zeolite in a 250 ml three-necked flask and disperse in 100 ml of aqueous solution, add an aqueous solution containing 4.5 g (0.1 mol) of ethylamine at 50° C., adjust the pH to 13 and stir for 4 hours. Then, 0.54 g (2 mmol) of ferric chloride hexahydrate aqueous solution (10 ml) was slowly added dropwise within 1 hour, and stirring was continued for 12 hours after the drop was completed. Then the stirring was stopped, the solid was filtered out, washed three times with methanol and deionized water respectively, and dried in vacuum at 100° C. to finally obtain 5.3 g of solid (yield: 87.7%).
Embodiment 2
[0018] In a 250ml three-necked flask, add 5g molecular sieves and disperse in 100ml ethanol solution, add 4.0g (0.05mol) pyridine at 70°C, adjust the pH value to 11 and stir for 4 hours. Then slowly add dropwise an ethanol solution (10 ml) containing 0.55 g (3 mmol) of copper acetate within 1 hour, and continue stirring for 12 hours after the drop is complete. Then the stirring was stopped, the solid was filtered out, washed three times with ethanol and deionized water respectively, and dried under vacuum at 100° C. to finally obtain 6.1 g of solid (yield: 63.9%).
Embodiment 3
[0020] In a 250ml three-necked flask, 5g of activated carbon was added and dispersed in 100ml of toluene, and an aqueous solution containing 4.65g (0.05mol) of aniline was added at 80°C to adjust the pH to 12 and stirred for 4 hours. Then, a methanol solution (10 ml) containing 0.9 g (5 mmol) of manganese nitrate was slowly added dropwise within 1 hour, and stirring was continued for 12 hours after the drop was completed. Then the stirring was stopped, the solid was filtered out, washed three times with methanol and deionized water respectively, and dried in vacuum at 100° C. to finally obtain 8.2 g of solid (yield: 77.7%).
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