Catalyst and preparation method for hydrogenation of acetic acid to ethanol
A catalyst and ethanol production technology, applied in chemical instruments and methods, preparation of hydroxyl compounds, organic compounds, etc., can solve problems such as large heat release, operating rate less than 60%, price drop of acetic acid, etc., to achieve mild reaction conditions, The effect of solving the overcapacity of acetic acid
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Embodiment 1
[0084](1) Add 54.45g of basic cobalt carbonate, 6g of molybdenum oxide, 14.89g of 85% phosphoric acid, and 5.18g of potassium nitrate into 100mL of deionized water, heat and dissolve at 100°C for 4 hours under constant stirring, and obtain clear and transparent Co-Mo-P-K mixture;
[0085] (2) Dissolving 128.2g of magnesium nitrate in the solution obtained in step (1) to form a Co-Mo-P-K-Mg mixed solution;
[0086] (3) After mixing 142g of silicon dioxide powder and 10g of scallop powder evenly, add the Co-Mo-P-K-Mg mixed solution prepared in step (2), knead and shape, dry at 120°C and roast at 400°C 4h, make catalyst precursor;
[0087] (4) Dissolve 2.66g of chloroplatinic acid in 100mL of deionized water, then put 200g of the catalyst precursor prepared in step (5) into the chloroplatinic acid solution for 2h, filter and dry at 200°C to obtain the catalyst. It is recorded as catalyst H, wherein the contents of Pt, Co, Mo, P, and K are 0.5%, 15%, 2%, 2%, and 1%, respectively...
Embodiment 2
[0089] (1) Add 54.45g of basic cobalt carbonate, 6g of molybdenum oxide, 14.89g of 85% phosphoric acid, and 5.18g of potassium nitrate into 100mL of deionized water, heat and dissolve at 100°C for 4 hours under constant stirring, and obtain clear and transparent Co-Mo-P-K mixture;
[0090] (2) Dissolving 128.2g of magnesium nitrate in the solution described in step (1) to form a Co-Mo-P-K-Mg mixed solution;
[0091] (3) Add the mixed solution prepared in step (2) to the silica sol (473.3g, containing 30% SiO 2 )-ammonia water (40mL) mixed solution, adjust the pH value of the solution to 5-6, continue to stir for 1h after the dropwise addition is complete, and let the precipitate age for 2h;
[0092] (4) Filter and wash the filter cake with deionized water until the conductivity of the washing solution is 10-100 μS / cm;
[0093] (5) Add 10g of squat powder to the filter cake, mix evenly, add 200mL of 5% dilute nitric acid solution, stir and form, dry at 120°C, and roast at 400...
Embodiment 3
[0096] (1) Add 54.45g of basic cobalt carbonate, 6g of molybdenum oxide, 14.89g of 85% phosphoric acid, and 5.18g of potassium nitrate into 100mL of deionized water, heat and dissolve at 100°C for 4 hours under constant stirring, and obtain clear and transparent Co-Mo-P-K mixture;
[0097] (2) Dissolving 128.2g of magnesium nitrate in the solution obtained in step (1) to form a Co-Mo-P-K-Mg mixed solution;
[0098] (3) After mixing 142g of silica powder and 10g of scallop powder evenly, add the Co-Mo-P-Mg mixed solution prepared in step (2), knead and shape, dry at 120°C and roast at 400°C 4h, make catalyst precursor;
[0099] (4) Dissolve 1.64g of platinum nitrate in 100mL of deionized water, then put 200g of the catalyst precursor prepared in step (5) into the platinum nitrate solution for 2h, filter and dry at 200°C to obtain the catalyst. It is recorded as catalyst J, wherein the content of Pt, Co, Mo, P, and K is 0.5%, 15%, 2%, 2%, and 1%, respectively, the content of c...
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