Catalyst for hydrogenation preparation of 1,3-propanediol from methyl 3-hydroxypropionate and preparation method of catalyst
A technology of methyl hydroxypropionate and catalyst, which is applied in the direction of preparation of hydroxy compounds, metal/metal oxide/metal hydroxide catalysts, chemical instruments and methods, etc., and can solve the problems that do not involve the order of addition and the method of addition, and are not clearly stated Hydrogenation conditions, poor catalytic effect, etc., to achieve the effects of enhanced interaction, prevention of sintering, and stable active centers
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Embodiment 1
[0027] Dissolve 39.48g of copper nitrate and 4.12g of manganese nitrate in 400mL of deionized water, and 465ml of 0.7mol / L sodium hydroxide solution at 45°C and 200rpm under stirring at 0.8ml / min, then add 20g of silica sol, wait After the pH of the precipitate is 12.0, it is aged at 66°C for 1 hour, washed three times, then vacuum-dried at 100°C for 24 hours, calcined at 500°C for 4 hours, sieved into 20-40 mesh and packed, at 450°C, 8.0MPa, with hydrogen Volume concentration 20vol.% Hydrogen-nitrogen mixed gas reduction for 1 hour, pass through a methanol solution of 3-hydroxypropionate with a mass concentration of 5%, react at 200°C, 6.0MPa, for 4 hours, take out the reacted liquid and use GC -7890A gas chromatograph analysis and determination, the evaluation results are shown in Table 1.
Embodiment 2
[0029] Dissolve 27.34g of copper nitrate, 3.72g of lanthanum nitrate, 2.34g of nickel nitrate in 400mL of deionized water, and 400ml of 0.3mol / L sodium hydroxide solution at 30°C and 600rpm with stirring at 6ml / min, and then add 30g Silica sol, after the pH of the precipitate is 7.0, age at 40°C for 6h, wash three times, vacuum dry at 60°C for 40 hours, bake at 850°C for 4 hours, sieve into 20~40 mesh and fill, at 200°C, 6.0MPa After reducing for 20 hours with a hydrogen-nitrogen mixed gas with a hydrogen volume concentration of 5vol.%, pass through a methanol solution of 3-hydroxypropionate with a mass concentration of 20%, react at 160°C and 8.0MPa for 20 hours, and take out the reaction The final liquid was analyzed and determined by GC-7890A gas chromatograph, and the evaluation results are shown in Table 1.
Embodiment 3
[0031] Dissolve 33.41g of copper nitrate, 2.19g of zinc nitrate, 1.47g of ammonium molybdate, and 0.60g of ammonium phosphate in 400mL of deionized water, and 480ml of 1.3mol / L sodium hydroxide solution at 60°C and 800rpm at 8ml / min Co-precipitate, then add 23.33g of silica sol, after the pH of the precipitate is 13.0, age at 100°C for 10h, wash twice, vacuum dry at 140°C for 4 hours, roast at 700°C for 18 hours, sieve into 20~40 mesh equipment, at 400°C, 0.01MPa, after 48h reduction with a hydrogen-nitrogen mixed gas with a hydrogen volume concentration of 10vol.%. MPa, react at lower temperature for 15 hours, take out the liquid after reaction and adopt GC-7890A gas chromatograph to analyze and measure, and the evaluation results are shown in Table 1.
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