Catalyst for use in catalytic conversion of carbon dioxide into methacrylic acid and application thereof
A carbon dioxide and catalyst technology, applied in the field of greenhouse gas carbon dioxide recycling and energy and environmental catalysis, can solve problems such as unsatisfactory selectivity
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Embodiment 1
[0047] Example 1H 6 PV 3 Mo 9 o 40 / CeO 2 Catalyst preparation and performance evaluation
[0048] Weigh 3.58gNa 2 HPO 4 2H 2 O was dissolved in 50ml distilled water and slightly heated to dissolve, and weighed 26.65gNa 2 MoO 4 2H 2 O, dissolved in 60ml of distilled water at 30°C, mixed the two solutions and heated to boiling with an electromagnetic stirrer, and reacted for 30 minutes. Weigh 0.91g vanadium pentoxide and dissolve in 10mL 1mol / dm -3 After the sodium carbonate solution, mix with the above solution and continue to react for 30 minutes. After cooling, adjust the pH to 2.0 with a sulfuric acid solution with a volume ratio of 1:1. Add 50ml of ether and 5ml of sulfuric acid solution with a volume ratio of 1:1 for extraction. Put the solution in two layers, put it in a fume hood for several days, blow out ether, put the solution in a vacuum desiccator at 80°C to evaporate the solvent for 3 hours, cool and crystallize to obtain orange-red crystal H 6 PV 3 M...
Embodiment 2
[0051] Example 2H 5 PW 11 Fe(H 2 O)O 39 / CeO 2 Catalyst preparation and performance evaluation
[0052] Weigh 14.6g phosphotungstic acid H 3 PW 12 o 40 In a three-necked bottle, add 30ml of water to dissolve, and weigh the equimolar FeSO 4 Dissolve the solid in it, slowly add saturated sodium carbonate solution to the solution at a constant temperature of 50°C to adjust the pH to 4.5, and stir at a constant temperature for 30 minutes, filter it into a beaker, evaporate the solvent at 90°C until it becomes semi-viscous, and after a few days it becomes a block Crystals precipitated to obtain H 5 PW 11 Fe(OH 2 )O 39 catalyst. Dry and grind for later use.
[0053] CeO 2 Dry at 200°C for 2 hours before use. Weigh 2.5g of catalyst and dissolve in 30ml of water-ethanol solution with a volume ratio of 1:1, then add 6.0g of CeO 2 , Ultrasonic dispersion at 30°C for 1h, standing still under constant stirring for 24h, drying at 120°C for 2h under vacuum conditions when th...
Embodiment 3
[0055] Example 3: Co 2.0 h 2.0 PMo 9 V 3 o 40 / CeO 2 Preparation and performance evaluation
[0056] Get the prepared H in Example 1 6 PV 3 Mo 9 o 40 , mixed with the nitrate of divalent metal cobalt in the solution according to the stoichiometric ratio, stirred at room temperature for 4.5h, and evaporated the solvent at 90°C to obtain Co 2.0 h 2.0 PMo 9 V 3 o 40 catalyst.
[0057] CeO 2 Dry at 200°C for 2 hours before use. Weigh 2.0g of catalyst and dissolve in 30ml of water-ethanol solution with a volume ratio of 1:1, then add 6.5g of CeO 2 , ultrasonically dispersed at 30°C for 1h, left to stand for 24h under constant stirring, dried at 120°C for 2h under vacuum conditions when the solvent evaporated into a gel, and then roasted at 300°C for 4h to obtain a loaded type with a solid loading capacity of 23.5wt%. catalyst.
[0058] co 2.0 h 2.0 PMo 9 V 3 o 40 / CeO 2 The catalyst performance evaluation experiment was carried out on a quartz tube fixed-bed r...
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