IP Library › Granted Patent US 12,276,067
Granted Patent B2
US 12,276,067 · App. 17/187,354 · Granted Apr 15, 2025

Modified alkanesulfonic acid and uses thereof

Inventors: Clay Purdy (Medicine Hat, CA); Markus Weissenberger (Calgary, CA); Kyle G. Wynnyk (Calgary, CA); Karl W. Dawson (Calgary, CA)
Assignee: SIXRING INC.
D21C3/06C01B15/08D21C3/006
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Quick Facts
Patent No.
US 12,276,067
App. No.
17/187,354
Granted
Apr 15, 2025
Kind
B2
Abstract

Method of delignification of plant material, said method comprising: providing said plant material comprising cellulose fibers and lignin; exposing said plant material requiring to a composition comprising: alkanesulfonic acid; and a peroxide, wherein said alkylsulfonic acid and peroxide are present in a molar ratio ranging 1:1 to 15:1 and the time of exposure is sufficient to remove substantially all of the lignin present on said plant material. Compositions capable of achieving delignification are also disclosed.

Claims (36)

1. An aqueous acidic composition comprising:

an alkylsulfonic acid;

a peroxide; and

a compound comprising an amine moiety selected from an alkanolamine,

wherein said alkylsulfonic acid is present in the composition in an amount ranging from 20 to 65 wt % of the total weight of the composition;

wherein said peroxide is present in the composition in an amount ranging from 1 to 30 wt % of the total weight of the composition; and

wherein said alkylsulfonic acid and said peroxide are present in the composition in a molar ratio of no less than 1:1.

2. The composition according to claim 1 , wherein said alkylsulfonic acid is selected from alkylsulfonic acids, wherein the alkyl in said alkylsulfonic acids is a linear or branched C1-C6 alkyl, and combinations thereof.

3. The composition according to claim 1 , wherein said alkylsulfonic acid is selected from methanesulfonic acid, ethanesulfonic acid, propanesulfonic acid, 2-propanesulfonic acid, isobutylsulfonic acid, t-butylsulfonic acid, butanesulfonic acid, iso-pentylsulfonic acid, t-pentylsulfonic acid, pentanesulfonic acid, t-butylhexanesulfonic acid, and combinations thereof.

4. The composition according to claim 1 , wherein said alkylsulfonic acid is methanesulfonic acid.

5. An aqueous composition comprising:

alkylsulfonic acid;

a peroxide; and

a compound comprising an amine moiety selected from an alkanolamine,

wherein said alkylsulfonic acid is present in the composition in an amount ranging from 20 to 65 wt % of the total weight of the composition;

wherein said peroxide is present in the composition in an amount ranging from 1 to 30 wt % of the total weight of the composition; and

wherein said alkylsulfonic acid and said peroxide are present in the composition in a molar ratio ranging from 1:1 to 15:1,

wherein said composition is suitable for delignifying biomass or wood.

6. The composition according to claim 5 , wherein said peroxide is hydrogen peroxide.

7. A method of delignifying biomass or plant material, said method comprising:

providing said biomass or plant material comprising cellulose fibers and lignin; and

exposing said biomass or plant material to a composition comprising:

alkylsulfonic acid;

a peroxide; and

a compound comprising an amine moiety selected from an alkanolamine,

wherein said alkylsulfonic acid is present in the composition in an amount ranging from 20 to 65 wt % of the total weight of the composition;

wherein said peroxide is present in the composition in an amount ranging from 1 to 30 wt % of the total weight of the composition; and

wherein said alkylsulfonic acid and said peroxide are present in the composition in a molar ratio ranging from 1:1 to 15:1;

for a period of time sufficient to remove substantially all lignin present on said biomass or plant material.

8. The method according to claim 7 , wherein said compound comprising an amine moiety has a molecular weight of less than 300 g/mol.

9. The method according to claim 7 , wherein said alkanolamine is selected from monoethanolamine, diethanolamine, triethanolamine, and combinations thereof.

10. The method according to claim 7 , wherein said alkanolamine is triethanolamine.

11. The method according to claim 7 , wherein said peroxide is hydrogen peroxide.

12. The composition of claim 1 , wherein said peroxide is hydrogen peroxide.

13. The composition according to claim 1 , wherein said alkanolamine is selected from monoethanolamine, diethanolamine, triethanolamine, and combinations thereof.

14. The composition according to claim 1 , wherein said alkanolamine is triethanolamine.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 26, 2021
From: PURDY, CLAY; WEISSENBERGER, MARKUS; WYNNYK, KYLE G.; DAWSON, KARL W.
To: SIXRING INC.
Reel/Frame 055433/0225 →
Priority Claims (1)
CA 3074198 · Feb 28, 2020 · national
Continuity (1)
Related Publication 20210269971A1 · Sep 2, 2021
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