Process for improved seaweed biomass conversion for fuel intermediates, agricultural nutrients and fresh water

Patent metadata

Field	Value
Publication number	US-9452993-B2
Application number	US-201314421093-A
Country	US
Kind code	B2
Filing date	Aug 12, 2013
Priority date	Aug 11, 2012
Publication date	Sep 27, 2016
Grant date	Sep 27, 2016

Abstract

The invention relates to an integrated process for the production of 5-hydroxymethyl furfural (HMF), K 2 SO 4 , levulinic acid and formic acid from κ-carrageenan, the latter being obtained from fresh Kappaphycus alvarezii seaweed biomass after expelling the juice. Mg(HSO 4 ) 2 was used in HMF synthesis, with co-production of galactose. The aqueous stream after HMF extraction was treated with the seaweed juice which process facilitated recovery of K 2 SO 4 in pure form. The galactose may be utilised for synthesis of levulinic acid and formic acid before or after K 2 SO 4 recovery or, alternatively, utilised for other purposes. Catalysts required in the synthetic reactions are generated in the process itself while the process energy required is met out of additional supplies of the seaweed biomass which is subjected to combustion/gasification.

First claim

The invention claimed is:

1. An integrated process for the production of fuel intermediates, agri-nutrients and potable water from Kappaphycus alvarezii seaweed comprising the steps of:
i. of mechanically shearing Kappaphycus alvarezii seaweed to obtain a slurry, and filtering the slurry to separate a first solid residual biomass from a first aqueous phase;
ii. mixing the first solid residual with seawater and incubating at 105° C.-120° C. at a pressure of 25 to 35 kPa for 50 to 70 minutes, then centrifuging to obtain an a second solid insoluble residue and a second aqueous phase, mixing the second aqueous phase with isopropyl alcohol and centrifuging to obtain κ-carrageenan as a solid;
iii. suspending the κ-carrageenan solid at 5-10% (w/v) in an aqueous solution containing an acid catalyst and incubating at 100-110° C. for 1-3 hours at 25-30 kPa to obtain a third aqueous phase comprising 5-hydroxymethyl furfural (HMF), galactose and potassium bisulphate;
iv. mixing the third aqueous phase with an organic solvent to obtain an organic phase containing HMF and a fourth aqueous phase, separating said organic phase from the fourth aqueous phase and extracting HMF from the organic phase to obtain recycled organic solvent;
v. optionally suspending additional κ-carrageenan solid into the fourth aqueous phase and repeating the process of step (iii), and repeating step (iv) with the recycled organic solvent;
vi. adding magnesium hydroxide to the fourth aqueous phase in an amount sufficient to achieve pH-neutral fourth aqueous phase;
vii. adding the first aqueous phase to the pH-neutral fourth aqueous phase to produce a fifth aqueous phase, and subjecting the fifth aqueous phase to evaporative concentration to obtain crystals of potassium sulphate and a sixth aqueous phase containing galactose;
viii. subjecting the sixth aqueous phase to further processing selected from (a) concentrating through evaporation to obtain crystals of galactose and a seventh aqueous phase (b) fermenting to obtain ethanol and a seventh aqueous phase or (c) adding dilute aqueous acid and incubating at 100-110° C. for 1-3hours at 25-30 kPa to obtain a levulinic acid and formic acid and a seventh aqueous phase;
ix. neutralizing the seventh aqueous phase and recovering magnesium hydroxide.

2. The process of claim 1 , wherein in step (ii) the yield of the κ-carrageenan is 45-55% by weight according to the weight of the first aqueous phase and the yield of the second solid insoluble residue is 30-35% by weight according to the weight of the first aqueous phase.

3. The process of claim 1 , wherein in step (iii) the acid catalyst is Mg(HSO 4 ) 2 or H 2 SO 4 .

4. The process of claim 3 , wherein the acid catalyst is Mg(HSO 4 ) 2 at a concentration of 0.33-0.63 M.

5. The process of claim 1 , wherein the 5-hydroxymethyl furfural (HMF) obtained in step (iii) contain 25-70% of the carbon in the κ-carrageenan.

6. The process of claim 1 , wherein in step (iv) the organic solvent is ethyl acetate.

7. The process of claim 1 , wherein in step (vii) the first aqueous phase has a KCl content of 3.5-4.2% (w/v).

8. The process of claim 1 , wherein water is condensed from them evaporative concentration in step (vii), wherein the water is passed through a carbon filter to eliminate odour.

9. The process of claim 1 , wherein in step (viii)(c) the dilute aqueous acid is HCl and the concentration of HCl is 1.0-5.0 M.

10. The process of claim 1 , further wherein the first aqueous phase or the seventh aqueous phase is further subjected to bipolar electro-dialysis (ED) to obtain HCl.

11. The process of claim 10 , wherein the bipolar ED of the first aqueous phase additionally gives KOH/NaOH.

12. The process of claim 1 , wherein in step (viii)(c) the yield of the levulinic acid and formic acid are together 80-85% by weight of the galactose.

13. The process of claim 1 , wherein in step (viii) the yield of HMF, levulinic acid and/or formic acid together contain 80-85% of the carbon in the κ-carrageenan.

14. The process of claim 1 , further comprising combusting or gasifying the first solid residual biomass to generate energy.

15. The process of claim 14 wherein the combustion or gasification further generates H 2 SO 4 and ash containing glasserite.

Assignees

• Council Scient Ind Res

Inventors

• Ghosh Pushpito Kumar
• MONDAL Dibyendu
• Maiti Pratyush
• Prasad Kamalesh
• Maiti Subarna
• Shah Bharti Gunvantray
• Siddhanta Arup Kumar

Classifications

• C02F2303/02

  Odour removal or prevention of malodour · CPC title

• C02F1/283

  using coal, charred products, or inorganic mixtures containing them · CPC title

• C07H3/02

  Monosaccharides · CPC title

• C02F1/04

  by distillation or evaporation · CPC title

• C05D1/00

  Fertilisers containing potassium (C05D7/00 takes precedence) · CPC title