Solid carbon-based Waugh-type molybdenum-containing heteropolyacid catalyst and application thereof
A technology of heteropoly acid and solid carbon, applied in the field of catalysis, can solve the problems of high cost, low catalytic efficiency, poor recovery, etc., and achieve the effects of easy recovery, improved catalytic performance, and shortened process time.
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Embodiment 1
[0021] Catalyst preparation:
[0022] Put 1.000g of activated carbon and 5ml of imidazole-4,5-dicarboxylic acid solution in a dilute acid solution with a pH of 3 prepared by sulfuric acid, add 0.2g of Waugh type manganese ammonium molybdate heteropolyacid, 1ml of octadecyl Dimethyl hydroxyethylenediyl ammonium nitrate, magnetically stirred at room temperature for 24 hours, then ultrasonically oscillated for 1 hour, moved into a hydrothermal reaction kettle, and used a temperature-programmed oven to raise the reaction temperature from room temperature to 150°C within 1 hour, and kept The temperature was kept for 48 hours, and then the temperature was naturally lowered to room temperature, washed several times with ultrapure water and ethanol respectively, filtered, and dried for 12 hours to obtain samples for later use.
[0023] Catalyst evaluation:
[0024] (1) The catalyst embodiment:
[0025] Dissolve 1.6667g of potassium iodide in an appropriate amount of deionized water,...
Embodiment 2
[0042] Catalyst preparation:
[0043] Put 1.000g of activated carbon and 5ml of imidazole-4,5-dicarboxylic acid solution in a dilute acid solution with a pH of 3 prepared by sulfuric acid, add 0.2g of ammonium polymolybdate, 1ml of octadecyldimethyl Hydroxyethylenediyl ammonium nitrate, magnetically stirred at room temperature for 24 hours, then ultrasonically oscillated for 1 hour, moved into a hydrothermal reaction kettle, and used a temperature-programmed oven to raise the reaction temperature from room temperature to 150°C within 1 hour, and kept the temperature for 48 hours, then cooled down to room temperature naturally, rinsed several times with ultrapure water and ethanol respectively, filtered, and dried for 12 hours to obtain samples for later use.
[0044] Catalyst evaluation:
[0045] Dissolve 1.6667g of potassium iodide in an appropriate amount of deionized water, transfer it to a 100mL volumetric flask, and adjust the volume to 0.01mol / L iodine solution, take 10...
Embodiment example 3
[0047] Catalyst preparation:
[0048] Put 1.000g of activated carbon and 5ml of imidazole-4,5-dicarboxylic acid solution in a dilute acid solution with a pH of 3 prepared by sulfuric acid, add 0.2g of Waugh type nickel ammonium molybdate heteropolyacid, 1ml of octadecyl Dimethyl hydroxyethylenediyl ammonium nitrate, magnetically stirred at room temperature for 24 hours, then ultrasonically oscillated for 1 hour, moved into a hydrothermal reaction kettle, and used a temperature-programmed oven to raise the reaction temperature from room temperature to 150°C within 1 hour, and kept The temperature was kept for 48 hours, and then the temperature was naturally lowered to room temperature, washed several times with ultrapure water and ethanol respectively, filtered, and dried for 12 hours to obtain samples for later use.
[0049] Catalyst evaluation:
[0050] Dissolve 1.6667g of potassium iodide in an appropriate amount of deionized water, transfer it to a 100mL volumetric flask, ...
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