Method for preparing alicyclic carboxylic acids and their esters
View Patent ↗A method for the continuous preparation of an alicyclic carboxylic acid or an ester of the alicyclic carboxylic acid. A plastic which incorporates the alicyclic carboxylic acid or an ester of the alicyclic carboxylic acid. An article made of a plastic which incorporates the alicyclic carboxylic acid or an ester of the alicyclic carboxylic acid. A liquid which incorporates the alicycic carboxylic acid or an ester of the alicyclic carboxylic acid.
1. A method for the continuous preparation of an alicyclic carboxylic acid or an ester thereof comprising
catalytically hydrogenating an aromatic carboxylic acid, an ester thereof, an anhydride thereof, or a mixture of two or more of these, with a hydrogen-comprising gas in the presence of at least one solid catalyst disposed in a fixed bed,
wherein the hydrogenation is carried out in at least three series-connected hydrogenation units;
wherein at least the first two series-connected hydrogenation units of the at least three series-connected hydrogenation units are operated in loop operating mode;
wherein the at least the first two series-connected hydrogenation unites operating in loop operating mode operate with different residence times, and
wherein the residence time in one of the at least first two series-connected hydrogenation units operating in loop operating mode is less than the residence time in a directly following hydrogenation unit operating in loop operating mode.
2. The method as claimed in claim 1 , wherein all hydrogenation units are operated in loop operating mode.
3. The method of claim 1 , wherein the last hydrogenation unit is operated in straight through-flow passage mode.
4. The method of claim 1 , wherein the hydrogenation is carried out in an apparatus comprising three hydrogenation units.
5. The method of claim 1 , wherein the at least one solid catalyst comprises at least one metal of the eighth subgroup of the Periodic Table of the Elements.
6. The method of claim 5 , wherein the at least one solid catalyst comprises ruthenium.
7. The method of claim 1 , wherein the at least one solid catalyst comprises a titanium dioxide support.
8. The method of claim 1 , wherein the ratio of the residence times in the series-connected loop reactors is from 0.01 to less than 1.
9. The method of claim 1 , wherein the aromatic carboxylic acid comprises an aromatic mono-, di- or poly-carboxylic acid.
10. The method of claim 9 , wherein the aromatic mono-, di- or polycarboxylic acid comprises benzene-, diphenyl-, naphthalene-, diphenyl oxide- or anthracene di- or poly-carboxylic acid.
11. The method of claim 9 , wherein the aromatic monocarboxylic acid comprises benzoic acid, 1-naphthoic acid, or 2-naphthoic acid.
12. The method as claimed in claim 11 , wherein the ester of the monocarboxylic acid is isononyl benzoate or decyl benzoate.
13. The method of claim 9 , wherein when the di- or poly-carboxylic acid is partially esterified, fully esterified, or a combination thereof.
14. The method of claim 9 , wherein the aromatic dicarboxylic acid is diisononyl phthalate or didecyl phthalate.
15. The method of claim 1 , wherein the ester of the aromatic carboxylic acid comprises at least one ester group comprising at least one alcohol comprising a branched or an unbranched alkoxyalkyl, cycloalkyl or alkyl group comprising 1 to 25 carbon atoms, or a combination thereof.
16. The method of claim 1 , wherein the ratio of the residence times in the series-connected loop reactors is from 0.01 to less than 1.