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The invention relates to a process for preparing a shaped Cu—Al catalyst body for the hydrogenation of organic compounds containing a carbonyl function. More particularly, the shaped catalyst body is suitable for the hydrogenation of aldehydes, ketones and of carboxylic acids or esters thereof, spec

The invention relates to a process for preparing a shaped Cu—Al catalyst body for the hydrogenation of organic compounds containing a carbonyl function. More particularly, the shaped catalyst body is suitable for the hydrogenation of aldehydes, ketones and of carboxylic acids or esters thereof, specifically of fatty acids or esters thereof, such as fatty acid methyl esters, to the corresponding alcohols such as butanediol. The present invention further relates to Cu—Al catalysts obtainable by the preparation process.

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1. A process for producing a tableted shaped catalyst body, which comprises the steps of: (a) combining of (i) at least one aqueous solution of copper compounds, aluminum compounds and optionally transition metal compounds and (ii) at least one aqueous carbonate-containing solution to form a precipi

1. A process for producing a tableted shaped catalyst body, which comprises the steps of: (a) combining of (i) at least one aqueous solution of copper compounds, aluminum compounds and optionally transition metal compounds and (ii) at least one aqueous carbonate-containing solution to form a precipitate, isolation of the precipitate, optionally washing of the isolated precipitate and drying of the isolated precipitate to give a dried precipitate, and(b) tableting of the dried precipitate obtained in step (a), wherein step (b) comprises:(b1) calcination of dried precipitate obtained in step (a) at a temperature in the range from 250 to 900° C., to give a calcined precipitate,(b2) mixing of dried precipitate obtained in step (a) with calcined precipitate obtained in step (b1) in a weight ratio of dried precipitate to calcined precipitate in the range from 2:98 to 98:2, to give a mixture, and(b3) tableting of the mixture obtained in step (b2). 2. The process according to claim 1, wherein a lubricant is added to the uncalcined precipitate obtained from step (a) or to the mixture obtained from step (b2) in an amount of from 0.1 to 5% by weight, based on the total weight of the composition to be tableted, before tableting. 3. The process according to claim 2, wherein the lubricant is added in an amount of from 0.5 to 5% by weight, based on the total weight of the composition to be tableted. 4. The process according to claim 2, wherein the lubricant is graphite. 5. The process according to claim 2, wherein the lubricant is added in an amount of from 1 to 4% by weight, based on the total weight of the composition to be tableted. 6. The process according to claim 1, wherein the pore volume of the tableted shaped catalyst body, determined by the Hg intrusion method in accordance with DIN 66133, is from 0.1 to 0.6 cm3/g. 7. The process according to claim 1, which comprises the following step: (c) after-calcination of the tableted shaped catalyst body at a temperature in the range from 250 to 900° C., to give an after-calcined shaped catalyst body. 8. The process according to claim 7, wherein the pore volume of the after-calcined shaped catalyst body, determined by the Hg intrusion method in accordance with DIN 66133, is from 0.15 to 0.70 cm3/g. 9. The process according to claim 8, wherein the pore volume of the after-calcined shaped catalyst body, determined by the Hg intrusion method in accordance with DIN 66133, is from 0.17 to 0.50 cm3/g. 10. The process according to claim 8, wherein the pore volume of the after-calcined shaped catalyst body, determined by the Hg intrusion method in accordance with DIN 66133, is from 0.19 to 0.4 cm3/g. 11. The process according to claim 7, wherein the step (c) takes places at temperature of about 750° C. 12. The process according to claim 7, which comprises the following step: (d) reduction of the tableted shaped catalyst body obtained from step (b) and/or the after-calcined shaped catalyst body obtained from step (c) to give a reduced shaped catalyst body. 13. The process according to claim 12, wherein reduction is effected by means of hydrogen. 14. The process according to claim 12, wherein reduction is carried out at a temperature in the range from 150° C. to 400° C. 15. The process according to claim 12, wherein reduction is carried out over a period of from 1 hour to 10 days. 16. The process according to claim 12, wherein (a) the reduced shaped catalyst body is covered with a liquid with exclusion of air after reduction, where the liquid is selected from the group consisting of isodecanol, fatty alcohols, hexadecane, 2-ethylhexanol, propylene glycol and mixtures thereof, or(b) a mixture of an oxygen-containing gas and an inert gas, wherein the oxygen-containing gas is oxygen and the inert gas is argon or nitrogen is fed into the reduction reactor containing the reduced shaped catalyst body, where the concentration of oxygen in the mixture during introduction is from 0.001% by volume to 50% by volume and is increased from about 0.02% by volume to about 21% by volume. 17. The process according to claim 7, wherein the step (c) takes place at a temperature in the range from 300 to 750° C. 18. The process according to claim 7, wherein the step (c) takes place at temperature in the range of 600 to 750° C. 19. The process according to claim 12, wherein reduction is carried out at a temperature in the range from 180° C. to 250° C. 20. The process according to claim 12, wherein reduction is carried out at a temperature in the range from 190° C. to 210° C. 21. The process according to claim 12, wherein reduction is carried out at, a temperature of about 200° C. 22. The process according to claim 12, wherein reduction is carried out over a period of from 2 hours to 72 hours. 23. The process according to claim 12, wherein reduction is carried out over a period of from 24 to 48 hours. 24. The process according to claim 1, wherein the precipitate obtained in step (a) has a carbonate content of up to 20% by weight inclusive, based on the total weight of the dried precipitate obtained in step (a). 25. The process according to claim 1, wherein the copper compound is selected from the group consisting of copper, copper oxide (Cu2O and/or CuO), copper nitrate, copper sulfate, copper carbonate, copper hydroxocarbonate, copper acetate, copper halides copper chloride, copper bromide or copper iodide and mixtures thereof. 26. The process according to claim 1, wherein the aluminum compound is selected from the group consisting of aluminum, aluminum hydroxide, aluminum oxide hydrate (boehmite), alkali metal aluminates, aluminum oxide (Al2O3), aluminum nitrate, aluminum sulfate, aluminum halides and mixtures thereof. 27. The process according to claim 1, wherein the transition metal compound is selected from the group consisting of Zn, Ti, Mn, Ni, Cr, Fe, Co, Mo, Ce and Zr and mixtures thereof. 28. The process according, to claim 1, wherein the carbonate-containing solution is obtained using at least one alkali metal carbonate, alkaline earth metal carbonate and/or ammonium carbonate and/or at least one alkali metal hydrogen carbonate, alkaline earth metal hydrogen carbonate and/or ammonium hydrogen carbonate. 29. The process according to claim 1, wherein step (b1) calcination of dried precipitate obtained in step (a) at a temperature in the range from 300 to 750° C., to give a calcined precipitate. 30. The process according to claim 1, wherein step (b1) calcination of dried precipitate obtained in step (a) at a temperature in the range from 600 to 750° C., to give a calcined precipitate. 31. The process according to claim 1, wherein the weight ratio of dried precipitate to calcined precipitate is in the range of from 10:90 to 90:10 to give a mixture. 32. The process according to claim 1, wherein the weight ratio of dried precipitate to calcined precipitate is in the range of from 15:85 to 85:15 to give a mixture. 33. The process according to claim 1, wherein the weight ratio of dried precipitate to calcined precipitate is in the range of from 20:80 to 50:50 to give a mixture. 34. The process according to claim 1, wherein the pore volume of the tableted shaped catalyst body, determined by the Hg intrusion method in accordance with DIN 66133, is from 0.13 to 0.40 cm3/g. 35. The process according to claim 1, wherein the pore volume of the tableted shaped catalyst body, determined by the Hg intrusion method in accordance with DIN 66133, is from 0.15 to 0.25 cm3/g. 36. The process according to claim 1, wherein the precipitate obtained in step (a) has a carbonate content range from 5% by weight to 18% by weight, based on the total weight of the dried precipitate obtained in step (a). 37. The process according to claim 1, wherein the precipitate obtained in step (a) has a carbonate content in the range from 6% by weight to 15% by weight, based on the total weight of the dried precipitate obtained in step (a). 38. The process according to claim 1, wherein the precipitate obtained in step (a) has a carbonate content in the range from 8 to 12% by weight, based on the total weight of the dried precipitate obtained in step (a). 39. The process according to claim 1, wherein the copper compound is selected from the group consisting of copper oxide, copper nitrate, copper chloride, copper carbonate, copper hydroxocarbonate, copper acetate, copper sulfate and mixtures thereof. 40. The process according to claim 1, wherein the aluminum compound is selected from the group consisting of aluminum nitrate, aluminum hydroxide, aluminum oxide hydrate, aluminum chloride, sodium aluminate, aluminum oxide and mixtures thereof. 41. The process according to claim 1, wherein the transition metal compound is selected from the group consisting of Mn, Zn, Ce, Zr and mixtures thereof. 42. The process according to claim 1, wherein the transition metal compound is from among compounds of Mn. 43. The process according to claim 1, wherein the carbonate-containing solution is obtained using sodium carbonate and/or sodium hydrogen carbonate. 44. A process for producing a tableted shaped catalyst body, which comprises the steps of: (a) combining of (i) at least one aqueous solution of copper compounds, aluminum compounds and optionally transition metal compounds and (ii) at least one aqueous carbonate-containing solution to form a precipitate, isolation of the precipitate, optionally washing of the isolated precipitate and drying of the isolated precipitate to give a dried precipitate, and(b) tableting of the dried precipitate obtained in step (a),wherein the precipitate obtained in step (a) contains at least 5% by weight of Cu hydroxocarbonate. 45. A process for producing a tableted shaped catalyst body, which comprises the steps of: (a) combining of (i) at least one aqueous solution of copper compounds, aluminum compounds and optionally transition metal compounds and (ii) at least one aqueous carbonate-containing solution to form a precipitate, isolation of the precipitate, optionally washing of the isolated precipitate and drying of the isolated precipitate to give a dried precipitate,(b) tableting of the dried precipitate obtained in step (a);(c) after-calcination of the tableted shaped catalyst body at a temperature in the range from 250 to 900° C., to give an after-calcined shaped catalyst bodywherein the pore volume of the tableted shaped catalyst body, determined by the Hp intrusion method in accordance with DIN 66133, is from 0.1 to 0.6 cm3/g; and(d) reduction of the tableted shaped catalyst body obtained from step (b) and/or the after-calcined shaped catalyst body obtained from step (c) to give a reduced shaped catalyst body,wherein (a) the reduced shaped catalyst body is covered with a liquid with exclusion of air after reduction, where the liquid is isodecanol. 46. A process for producing a tableted shaped catalyst body, which comprises the steps of: (a) combining of (i) at least one aqueous solution of copper compounds, aluminum compounds and optionally transition metal compounds and (ii) at least one aqueous carbonate-containing solution to form a precipitate, isolation of the precipitate, optionally washing of the isolated precipitate and drying of the isolated precipitate to give a dried precipitate, (b) tableting of the dried precipitate obtained in step (a),(c) after-calcination of the tableted shaped catalyst body at a temperature in the range from 250 to 900° C., to give an after-calcined shaped catalyst body,wherein the pore volume of the tableted shaped catalyst body, determined by the Hg intrusion method in accordance with DIN 66133, is from 0.1 to 0.6 cm3/g, and (d) reduction of the tableted shaped catalyst body obtained from step (b) and/or the after-calcined shaped catalyst body obtained from step (c) to give a reduced shaped catalyst body, wherein(a1) the reduced shaped catalyst body is covered with a liquid with exclusion of air after reduction, where the liquid is selected from the group consisting of isodecanol, fatty alcohols, hexadecane, 2-ethylhexanol, propylene glycol and mixtures thereof, or(b1) a mixture of an oxygen-containing gas and an inert gas, wherein the oxygen-containing gas is oxygen and the inert gas is argon or nitrogen, is fed into the reduction reactor containing the reduced shaped catalyst body, where the concentration of oxygen in the mixture during introduction is from 0.001% by volume to 50% by volume and is increased from about 0.02% by volume to about 21% by volume. 47. A process for producing a tableted shaped catalyst body, which comprises the steps of: (a) combining of (i) at least one aqueous solution of copper compounds, aluminum compounds and optionally transition metal compounds and (ii) at least one aqueous carbonate-containing solution to form a precipitate, isolation of the precipitate, optionally washing of the isolated precipitate and drying of the isolated precipitate to give a dried precipitate, and(b) tableting of the dried precipitate obtained in step (a)wherein the precipitate obtained in step (a) contains from 10 to 80% by weight, of Cu hydroxocarbonate. 48. A process for producing a tableted shaped catalyst body, which comprises the steps of: (a) combining of (i) at least one aqueous solution of copper compounds, aluminum compounds and optionally transition metal compounds and (ii) at least one aqueous carbonate-containing solution to form a precipitate, isolation of the precipitate, optionally washing of the isolated precipitate and drying of the isolated precipitate to give a dried precipitate, and(b) tableting of the dried precipitate obtained in step (a),wherein the precipitate obtained in step (a) contains from 15 to 70% by weight, of Cu hydroxocarbonate.