Biorefinery of brown macroalgae

Patent metadata

Field	Value
Publication number	US-11230611-B2
Application number	US-201816765492-A
Country	US
Kind code	B2
Filing date	Nov 21, 2018
Priority date	Nov 21, 2017
Publication date	Jan 25, 2022
Grant date	Jan 25, 2022

Abstract

The present invention concerns an improved process for biorefinery of brown macroalgae, which comprises: (a) contacting the brown macroalgae with a solvent system comprising at least 30 wt % organic solvent, to obtain extracted macroalgae as solid residue and a liquor; and (b) biorefining the extracted macroalgae. The inventors have found that the contacting of step (a) results in an efficient and cost-effective dewatering of the macroalgae, wherein up to 95 wt % of the internal moisture of the macroalgae could be lost without the need for energy-consuming drying techniques. As such, the downstream biorefinery of the extracted macroalgae is greatly facilitated.

First claim

The invention claimed is:

1. A process for biorefining brown macroalgae, comprising:
(a) contacting the brown macroalgae with a solvent system comprising at least 30 wt % of a ketone organic solvent, wherein water is expelled from the macroalgae, to obtain extracted macroalgae as solid residue and a liquor comprising expelled water;
(b) biorefining the extracted macroalgae; and
(c) isolating mannitol from the liquor by separation of the organic solvent and water.

2. The process according to claim 1 , wherein step (b) involves one or more of alginate isolation, hydrolysis of alginate and/or cellulose, fermentation of the extracted macroalgae and isolation of proteins.

3. The process according to claim 1 , wherein the extracted macroalgae are stored for at least one month prior to being subjected to step (b).

4. The process according to claim 1 , wherein the brown macroalgae belongs to the genera Laminaria, Saccharina, Sargassum, Macrocystis, Nereocystis, Lessonia, Alaria, Ascophyllum and/or Fucus.

5. The process according to claim 1 , wherein the organic solvent is miscible with water at all ratios.

6. The process according to claim 1 , wherein the organic solvent is acetone or methyl ethyl ketone.

7. The process according to claim 1 , wherein the amount of organic solvent in the solvent system is such that the organic solvent to water weight ratio, taking into account the water present in the macroalgae, is in the range of 10/90-90/10.

8. The process according to claim 1 , wherein step (a) is performed at a temperature in the range of 10-100° C.

9. The process according to claim 1 , wherein the solvent system comprises acetone and step (a) is performed at a temperature in the range of 30-80° C.

10. The process according to claim 1 , wherein the contacting of step (a) is performed in counter-current mode.

11. The process according to claim 1 , wherein the solvent system step (a) comprises at least 75 wt % organic solvent.

12. The process according to claim 1 , wherein step (c) further involves the isolation of laminarin.

13. The process according to claim 1 , wherein the solvent separated in step (c) is recycled to step (a).

14. The process according to claim 1 , wherein the solvent system comprises at least 75 wt % acetone, and step (b) involves alkaline liquefaction, wherein alginate is separated from the extracted macroalgae.

15. The process according to claim 2 , wherein step (b) involves at least alginate isolation.

16. The process according to claim 6 , wherein the organic solvent is acetone.

17. The process according to claim 7 , wherein the amount of organic solvent in the solvent system is such that the organic solvent to water weight ratio, taking into account the water present in the macroalgae, is in the range of 35/65-80/20.

18. The process according to claim 8 , wherein step (a) is performed at a temperature in the range of 30-80° C.

19. The process according to claim 9 , wherein step (a) is performed at a temperature in the range of 45-75° C.

20. The process according to claim 11 , wherein the solvent system step (a) comprises 80-95 wt % organic solvent.

Assignees

• TNO

Inventors

• Smit Adrianus Theodorus
• Huijgen Wouter Johannes Joseph

Classifications

• C08B37/0003 Primary

  General processes for their isolation or fractionation, e.g. purification or extraction from biomass · CPC title

• C07C29/76

  by physical treatment · CPC title

• C08L5/04

  Alginic acid; Derivatives thereof · CPC title

• C08B37/0084

  Guluromannuronans, e.g. alginic acid, i.e. D-mannuronic acid and D-guluronic acid units linked with alternating alpha- and beta-1,4-glycosidic bonds; Derivatives thereof, e.g. alginates · CPC title

• C08B37/0024

  beta-D-Glucans; (beta-1,3)-D-Glucans, e.g. paramylon, coriolan, sclerotan, pachyman, callose, scleroglucan, schizophyllan, laminaran, lentinan or curdlan; (beta-1,6)-D-Glucans, e.g. pustulan; (beta-1,4)-D-Glucans; (beta-1,3)(beta-1,4)-D-Glucans, e.g. lichenan; Derivatives thereof · CPC title