Method for post-treating polyol esters
View Patent ↗A batchwise process for aftertreatment of polyol esters prepared by reacting polyols of the general formula (II) H—(—O—[—CR 1 R 2 —] m —) o —OH (II) in which R 1 and R 2 are each independently hydrogen, an alkyl radical having 1 to 5 carbon atoms, preferably methyl, ethyl or propyl, or a hydroxyalkyl radical having 1 to 5 carbon atoms, preferably the hydroxymethyl radical, m is an integer from 1 to 10, preferably 1 to 8 and especially 1, 2, 3 or 4, o is an integer from 2 to 15, preferably 2 to 8 and especially 2, 3, 4 or 5, with excess linear or branched aliphatic monocarboxylic acids having 3 to 20 carbon atoms and having a lower boiling point than the polyols used. The process is carried out in the presence of a Lewis acid and in the presence of an adsorbent, while removing the water formed, characterized in that the excess monocarboxylic acid is removed by distillation and water is added to the crude ester obtained at a temperature below the boiling point of water at the particular pressure and the crude ester with added water is aftertreated with avoidance of basic compounds, and the sparingly soluble conversion products and the adsorbent present in the esterification reaction are filtered off.
1. A batchwise process for aftertreatment of polyol esters prepared by reacting polyols of the general formula (II)
H—(—O—[—CR 1 R 2 —] m —) o —OH (II)
in which R 1 and R 2 are each independently selected from the group consisting of hydrogen, an alkyl radical having 1 to 5 carbon atoms or a hydroxyalkyl radical having 1 to 5 carbon atoms, m is an integer from 1 to 10, o is an integer from 2 to 15, with excess of linear or branched aliphatic monocarboxylic acids having 3 to 20 carbon atoms and having a lower boiling point than the polyols used, in the presence of a Lewis acid selected from the group consisting of titanium, zirconium, hafnium, iron, zinc, boron, aluminum and tin as elements or in the form of compounds thereof as catalyst and in the presence of an adsorbent in an amount of 0.1 to 5 parts by weight per 100 parts by weight of a reaction mixture, while removing the water formed, characterized in that the excess monocarboxylic acid is removed by distillation and water is added to the crude ester obtained at a temperature below the boiling point of water at the particular pressure and the crude ester with added water is aftertreated with avoidance of basic compounds, and the sparingly soluble conversion products and the adsorbent present in the esterification reaction are filtered off.
2. The process as claimed in claim 1 , characterized in that water is added in an amount of 0.5% to 5% by weight, based on the polyol ester to be aftertreated.
3. The process as claimed in claim 1 , characterized in that the aftertreatment with water is effected under standard pressure at a temperature of 40 to below 100° C.
4. The process as claimed in claim 1 , characterized in that the aftertreatment with water is effected above standard pressure and at a temperature of at least 100° C.
5. The process as claimed in claim 1 , characterized in that the aftertreatment with water is conducted over a period of 10 minutes to 4 hours.
6. The process as claimed in claim 1 , characterized in that the water which is recovered by condensation of steam used to generate heat or reduced pressure is used for the aftertreatment.
7. The process as claimed in claim 1 , characterized in that the aftertreatment with water is followed by a further treatment with hydrogen peroxide, immediately followed by a steam treatment.
8. The process as claimed in claim 1 for aftertreatment of triethylene glycol di-2-ethylhexanoate, tetraethylene glycol di-n-heptanoate, triethylene glycol di-2-ethylbutyrate, triethylene glycol di-n-heptanoate or tetraethylene glycol di-2-ethylhexanoate.
9. The process as claimed in claim 1 , in which R 1 and R 2 are each independently hydrogen, an alkyl radical selected from: methyl, ethyl or propyl; or a hydroxyalkyl radical having 1 to 5 carbon atoms.
10. The process as claimed in claim 1 , wherein the hydroxyalkyl radical is hydroxymethyl radical.
11. The process as claimed in claim 1 , wherein m is an integer from 1 to 8.
12. The process as claimed in claim 1 , wherein m is 1, 2, 3 or 4.
13. The process as claimed in claim 1 , wherein o is an integer from 2 to 8.
14. The process as claimed in claim 1 , wherein o is 2, 3, 4 or 5.
15. The process as claimed in claim 1 , wherein the adsorbent is present in an amount of from 0.5 to 1.5 parts by weight per 100 parts by weight of the reaction mixture.
16. The process as claimed in claim 1 , characterized in that water is added in an amount of 1% to 4% by weight, based on the polyol ester to be aftertreated.
17. The process as claimed in claim 1 , characterized in that the aftertreatment with water is effected under standard pressure at a temperature of from 60 to 90° C.
18. The process as claimed in claim 1 , characterized in that the aftertreatment with water is conducted over a period of 30 minutes to 2 hours.
19. The process as claimed in claim 2 , characterized in that the aftertreatment with water is effected under standard pressure at a temperature of 40 to below 100° C.
20. The process as claimed in claim 2 , characterized in that the aftertreatment with water is effected above standard pressure and at a temperature of at least 100° C.