IP Library Patent Application 18259002
Patent Application
App. No. 18/259,002

METHOD FOR PRODUCING GLYCOLIC ACID

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Quick Facts
Patent No.
US None
App. No.
18/259,002
Abstract

A method for producing glycolic acid includes selectively hydrogenating glyoxylic acid using a catalyst comprising at least one transition metal element, the glycolic acid produced, which has a bio-based carbon content of above 50%. A method for preparing a composition selected from the group consisting of cosmetics, home care products, personal care products, textiles, food, beverages, drugs, fragrances, inks, or paints includes adding the glycolic acid to the composition.

Claims (26)

1 . A method for producing glycolic acid comprising selectively hydrogenating glyoxylic acid, wherein the glycolic acid is selectively hydrogenated in the presence of a catalyst comprising at least one transition metal element.

2 . The method according to claim 1 , wherein the catalyst is a heterogeneous catalyst.

3 . The method according to claim 1 , wherein glyoxylic acid is selectively hydrogenated in the presence of a reaction medium.

4 . The method according to claim 3 , wherein the reaction medium consists of water.

5 . The method according to claim 3 , wherein the reaction medium comprises water and at least one another solvent selected from the group consisting of ethanol, acetone, acetonitrile, methanol, and combinations thereof.

6 . The method according to claim 1 , wherein the catalyst is in solid form.

7 . The method according to claim 1 , wherein the transition metal element is selected from the group consisting of Fe, Co, Ni, Cu, Zn, Ru, Rh, Pd, Ag, Pt and Au.

8 . The method according to claim 1 , wherein the transition metal element is not supported on a support.

9 . The method according to claim 1 , wherein the transition metal element is supported on a support selected from the group consisting of activated carbon, Al 2 O 3 , SiO 2 , TiO 2 , ZrO 2 , molecular sieve, and combinations thereof.

10 . The method according to claim 1 , wherein the transition metal element is supported on a support, which is not a nanotube.

11 . The method according to claim 1 , wherein the catalyst is selected from the group consisting of 5 wt % Pd/C, Ni, and combinations thereof.

12 . The method according to claim 1 , wherein the glyoxylic acid is selectively hydrogenated in the presence of a hydrogen gas.

13 . The method according to claim 1 , wherein the glyoxylic acid is selectively hydrogenated at a pressure in the range of 1 atm to 50 bars.

14 . The method according to claim 1 , wherein the glyoxylic acid is selectively hydrogenated at a temperature from room temperature to 200° C.

15 . The method according to claim 1 , wherein the glyoxylic acid is selectively hydrogenated with a glyoxylic acid conversion rate of no less than 40%.

16 . The method according to claim 1 , wherein the glyoxylic acid is selectively hydrogenated with a glycolic acid selection rate of 40% to 90%.

17 . The method according to claim 1 , wherein the concentration of glyoxylic acid in the reaction medium is in the range of 1-50 wt % relative to the total weight of glyoxylic acid and the reaction medium.

18 . The method according to claim 1 , wherein the content of the catalyst is in the range of 1-20 wt % relative to the weight of the glyoxylic acid.

19 . The method according to claim 1 , wherein the glyoxylic acid is selectively hydrogenated in a duration in the range of 2-10 hours.

20 . A glycolic acid produced by or derived from the method according to claim 1 , wherein the glyoxylic acid has a bio-based carbon content of above 50%.

21 . The glycolic acid according to claim 20 having a mean isotopic 13C deviation of from −29‰ to −7‰.

22 . The glycolic acid according to claim 20 having a mean isotopic deviation of from −7‰ to −3‰.

23 . A glycolic acid with a bio-based carbon content of above 50% and below 100%.

24 . The glycolic acid according to claim 23 having a mean isotopic 13C deviation of from −29‰ to −3‰.

25 . The glycolic acid according to claim 23 having a mean isotopic deviation of from −7‰ to −3‰.

26 . (canceled)

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 26, 2024
From: RHODIA OPERATIONS
To: SPECIALTY OPERATIONS FRANCE
Reel/Frame 066374/0642 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 20, 2023
From: SU, FANGZHENG; STORET, ISABELLE; STREIFF, STEPHANE
To: RHODIA OPERATIONS
Reel/Frame 065298/0847 →