Process for recovering aliphatic monocarboxylic acids from distillation
View Patent ↗A process is provided for recovering aliphatic monocarboxylic acids having from 4 to 11 carbon atoms from the distillation residue obtained in the oxidation of the corresponding aldehyde by means of oxygen or oxygen-containing gas mixtures in the presence of alkali metal carboxylates or alkaline earth metal carboxylates to form the corresponding monocarboxylic acid and subsequent distillation, characterized in that the distillation residue is reacted with an aqueous acid in a tube reactor and the two-phase mixture flowing out from the tube reactor is introduced into a settling vessel in which the organic phase which separates out has a pH of 4.5 or less.
1. A process for recovering aliphatic monocarboxylic acids having from 4 to 11 carbon atoms from the distillation residue obtained in the oxidation of the corresponding aldehyde by means of oxygen or oxygen-containing gas mixtures in the presence of alkali metal carboxylates or alkaline earth metal carboxylates to form the corresponding monocarboxylic acid and subsequent distillation, characterized in that the distillation residue is reacted with an aqueous acid in a tube reactor and the two-phase mixture flowing out from the tube reactor is introduced into a settling vessel in which the organic phase which separates out has a pH of 4.5 or less.
2. The process according to claim 1 , characterized in that a static mixing element is installed upstream of the tube reactor.
3. The process according to claim 1 , characterized in that the tube reactor contains packing elements or internals.
4. The process according to claim 1 , characterized in that the distillation residue is preheated to a temperature of from 30 to 90° C.
5. The process according to claim 1 , characterized in that the reaction is carried out at a temperature of from 30 to 90° C.
6. The process according to claim 1 , characterized in that an aqueous solution of an inorganic acid is used as aqueous acid.
7. The process according to claim 6 , characterized in that hydrochloric acid, sulphuric acid, phosphoric acid or nitric acid is used as inorganic acid.
8. The process according to claim 1 , characterized in that the distillation residues from the preparation of aliphatic straight-chain or branched monocarboxylic acids are used.
9. The process according to claim 8 , characterized in that the distillation residues from the preparation of aliphatic straight-chain monocarboxylic acids selected from the group consisting of n-butyric acid, n-pentanoic acid, n-hexanoic acid, n-heptanoic acid, n-octanoic acid, n-nonanoic acid and n-decanoic acid are used.
10. The process according to claim 8 , characterized in that the distillation residues from the preparation of aliphatic, α-alkyl-branched monocarboxylic acids are used.
11. The process according to claim 10 , characterized in that isobutyric acid, 2-ethylbutyric acid, 2-methylbutyric acid, 2-methylpentanoic acid, 2-methylhexanoic acid, 2-ethylhexanoic acid, 2-methyloctanoic acid, 2-methylnonanoic acid, 2-propylheptanoic acid, 2-ethylbutenoic acid, 2-methylpentenoic acid, 2-ethylhexenoic acid or 2-propylheptenoic acid is used as aliphatic, α-alkyl-branched monocarboxylic acid.
12. The process according to claim 8 , characterized in that the distillation residues from the preparation of aliphatic branched monocarboxylic acids which are not α-alkyl-branched are used.
13. The process according to claim 12 , characterized in that an isopentanoic acid having any branching, isohexanoic acid having any branching, isoheptanoic acid having any branching, isooctanoic acid having any branching, isononanoic acid having any branching, isodecanoic acid having any branching or isoundecanoic acid having any branching is used as aliphatic branched monocarboxylic acid, with the proviso that there is no α-alkyl branching.
14. The process according to claim 13 , characterized in that 3-methylbutyric acid is used as isopentanoic acid having any branching.
15. The process according to claim 13 , characterized in that an isononanoic acid having the main constituent 3,5,5-trimethylhexanoic acid is used as isononanoic acid having any branching.
16. The process according to one or more of claim 1 , characterized in that the potassium carboxylate- or sodium carboxylate-containing distillation residues of the corresponding monocarboxylic acids are reacted with the aqueous acid.
17. The process according to claim 1 , characterized in that the distillation residue is preheated to a temperature of from 50 to 80° C.
18. The process according to claim 1 , characterized in that the reaction is carried out at a temperature of from 50 to 80° C.
19. The process according to claim 5 , characterized in that an aqueous solution of an inorganic acid is used as aqueous acid.
20. The process according to claim 19 , characterized in that hydrochloric acid, sulphuric acid, phosphoric acid or nitric acid is used as inorganic acid.