Organic solvent pretreatment of biomass to enhance enzymatic saccharification
View Patent ↗Biomass is pretreated using an organic solvent solution under alkaline conditions in the presence of ammonia and optionally an additional nucleophile to fragment and extract lignin without loss of hemicellulose. Pretreated biomass is further hydrolyzed with a saccharification enzyme consortium. Fermentable sugars released by saccharification may be utilized for the production of target chemicals by fermentation.
1. A method for producing fermentable sugars comprising:
(a) providing lignocellulosic biomass comprising lignin, cellulose and hemicellulose;
(b) suspending the biomass of (a) in an organic solvent solution comprising water, ammonia in an amount of about 2% to about 20% relative to weight of dry biomass and one or more nucleophile, whereby a biomass-solvent suspension is formed under alkaline conditions;
(c) heating the biomass-solvent suspension to a temperature of about 100-220° C. for about 5 minutes to about 5 hours whereby lignin is fragmented and is dissolved in the suspension;
(d) filtering free liquid under pressure after heating the suspension in (c) whereby the dissolved lignin is removed and whereby carbohydrate-enriched biomass with high retention of hemicellulose is produced;
(e) optionally washing the carbohydrate-enriched biomass of (d) with an organic solvent solution producing a solvent-washed carbohydrate-enriched biomass;
(f) removing solvent from the carbohydrate-enriched biomass of (e), or of (d) when (e) is omitted;
wherein a readily saccharifiable carbohydrate-enriched biomass is produced; and
(g) contacting the readily saccharifiable carbohydrate-enriched biomass of (f) with an enzyme consortium,
whereby fermentable sugars are produced.
2. The method of claim 1 wherein removing solvent is by washing with water or drying.
3. The method of claim 1 wherein step (e) is repeated one or more times.
4. The method of claim 1 further comprising fermenting the sugars to produce a target product.
5. The method of claim 4 wherein the target product is selected from the group consisting of alcohols, organic acids, amino acids and gases.
6. The method of claim 5 wherein the target product is selected from the group consisting of ethanol, butanol, or 1,3-propanediol.
7. The method of claim 1 , wherein said one or more nucleophile is selected from the group consisting of NaOH, one or more alkylamines, sulfide, hydrosulfide, polysulfide, hydropolysulfide, thiol reagents, and combinations thereof.
8. The method of claim 7 wherein the one or more alkylamines is selected from the group consisting of R—NH 2 , R 2 —NH, R 3 N, (H 2 N—R—NH 2 ), (H 2 N—R(NH 2 ) 2 ), (HO—R—NH 2 ), ((HO) 2 —R—NH 2 ), (HO—R—(NH 2 ) 2 ), (HS—R—NH 2 ), ((HS) 2 —R—NH 2 ), (HS—R—(NH 2 ) 2 ) and (H 2 N—R(OH)(SH) and combinations thereof, wherein R is independently a monovalent, divalent or trivalent 1-6 carbon alkane, alkene or alkyne, linear, cyclic or branched.
9. The method of claim 8 wherein R is independently methyl, ethyl, propyl or butyl.
10. The method of claim 8 wherein the alkylamine is methylamine.
11. The method of claim 8 wherein the alkylamine is at a concentration of less than about 20% relative to dry weight of biomass.
12. The method of claim 1 wherein the solvent solution to biomass in step (b) has a weight ratio of about 10 to 1 to 0.5 to 1.
13. The method of claim 1 , wherein the heated suspension of step (c) is cooled to room temperature before filtering in step (d).
14. The method of claim 1 wherein the biomass is selected from the group consisting of switchgrass, waste paper, sludge from paper manufacture, corn fiber, corn cobs, corn husks, corn stover, grasses, wheat, wheat straw, hay, barley, barley straw, rice straw, sugar cane bagasse, sugar cane straw, yellow poplar, sorghum, soy, components obtained from processing of grains, trees, branches, roots, leaves, wood chips, sawdust, shrubs and bushes, vegetables, fruits, flowers, animal manure and combinations thereof.
15. The method of claim 1 wherein the organic solvent solution of (b) further comprises one or more additional components selected from the group consisting of alkali or alkaline earth hydroxides or carbonates, ammonia, thiols, sulfides, hydrosulfides, polysulfides, hydropolysulfides, and combinations thereof.
16. The method of claim 1 wherein the organic solvent solution of (b) and any ammonia or other unreacted components are recyclable.
17. The method of claim 1 wherein the organic solvent solution of (b) and the organic solvent solution of (e) comprise a solvent independently selected from the group consisting of alcohols, diols and aprotic solvents.
18. The method of claim 17 wherein the organic solvent solution comprises a solvent selected from the group consisting of methanol, ethanol, propanol, butanol, pentanol and hexanol, isomers thereof, and diols thereof.
19. The method of claim 18 wherein the organic solvent solution comprises from about 40% to about 70% ethanol in water.