IP Library Granted Patent US 12679793
Granted Patent B2
US 12679793 · App. 18/548,417 · Granted Jul 14, 2026

Recovery of diols from a mixture

Inventor: Marco Cotti Comettini (Brusnengo, IT)
Assignee: NOVAMONT S.P.A.
C07C29/80C07C29/76
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Quick Facts
Patent No.
US 12679793
App. No.
18/548,417
Granted
Jul 14, 2026
Kind
B2
Abstract

The present invention relates to a process for purifying diols obtained by fermentation, in particular to increase their recovery during distillation operations.

Claims (23)

1 . A process for the recovery of diol from a mixture comprising at least one diol and higher boiling compounds, having a higher boiling point than that of the diol, said process comprising the steps of:

(a) subjecting the said mixture to distillation, separating a fraction enriched in said higher boiling compounds;

(b) diluting said enriched fraction separated in step (a) with water;

(c) subjecting the fraction diluted in step (b) to one or more filtration operations, by separating a permeate comprising the diol from a retentate comprising the higher boiling compounds.

2 . The process according to claim 1 , in which the mixture comprises at least one diol selected from: 1,2-ethanediol, 1,2-propanediol, 1,3-propanediol, 1,3-butanediol, 1,4-butanediol, 2,3-butanediol, 1,2-pentanediol, 1,3-pentanediol, 1,4-pentanediol, 1,5-pentanediol, 1,6-hexanediol, 1,7-heptanediol, 1,8-octanediol, 1,9-nonanediol, 1,10-decanediol, 1,11-undecanediol, 1,12-dodecanediol, 1,13-tridecanediol 1,4-cyclohexanedimethanol, neopentylglycol, 2-methyl-1,3-propanediol, 3-methyl-1,5-pentanediol, 2-methyl-1,8-octanediol, 2,2-diethyl-1,3-propanediol, dianhydrosorbitol, dianhydromannitol, dianhydroiditol, cyclohexanediol, cyclohexanmethanediol, dialkylene glycols, polyalkylene glycols and mixtures thereof.

3 . The process according to claim 2 , wherein said at least one diol is a linear C2-C6 aliphatic diol.

4 . The process according to claim 3 , wherein said C2-C6 aliphatic diol is selected from 1,2-ethanediol, 1,2-propanediol, 1,3-propanediol, 1,3-butanediol, 1,4-butanediol, 2,3-butanediol, 2-methyl-1,3-propanediol and mixtures thereof.

5 . The process according to claim 4 , wherein said C2-C6 aliphatic diol is 1,3-butanediol and/or 1,4-butanediol.

6 . The process according to claim 1 , wherein the enriched fraction separated in step a) has a content of more than 40% by weight of compounds having a higher boiling point than that of the diol, relative to the weight of the enriched fraction.

7 . The process according to claim 1 , in which the enriched fraction separated in step a) has a diol content of 10% to 60% by weight relative to the total weight of the enriched fraction.

8 . The process according to claim 1 , wherein the filtration operations in step c) comprise ultrafiltration and/or nanofiltration.

9 . The process according to claim 8 , wherein the filtration operations in step c) comprise nanofiltration.

10 . The process according to claim 1 , wherein said filtration operations in step c) are conducted in multiple stages.

11 . The process according to claim 2 , wherein the enriched fraction separated in step a) has a content of more than 40% by weight of compounds having a higher boiling point than that of the diol, relative to the weight of the enriched fraction.

12 . The process according to claim 3 , wherein the enriched fraction separated in step a) has a content of more than 40% by weight of compounds having a higher boiling point than that of the diol, relative to the weight of the enriched fraction.

13 . The process according to claim 4 , wherein the enriched fraction separated in step a) has a content of more than 40% by weight of compounds having a higher boiling point than that of the diol, relative to the weight of the enriched fraction.

14 . The process according to claim 5 , wherein the enriched fraction separated in step a) has a content of more than 40% by weight of compounds having a higher boiling point than that of the diol, relative to the weight of the enriched fraction.

15 . The process according to claim 2 , in which the enriched fraction separated in step a) has a diol content of 10% to 60% by weight relative to the total weight of the enriched fraction.

16 . The process according to claim 3 , in which the enriched fraction separated in step a) has a diol content of 10% to 60% by weight relative to the total weight of the enriched fraction.

17 . The process according to claim 4 , in which the enriched fraction separated in step a) has a diol content of 10% to 60% by weight relative to the total weight of the enriched fraction.

18 . The process according to claim 5 , in which the enriched fraction separated in step a) has a diol content of 10% to 60% by weight relative to the total weight of the enriched fraction.

19 . The process according to claim 6 , in which the enriched fraction separated in step a) has a diol content of 10% to 60% by weight relative to the total weight of the enriched fraction.

20 . The process according to claim 2 , wherein the filtration operations in step c) comprise ultrafiltration and/or nanofiltration.