A process for the conversion of a solid lignocellulosic material

Patent metadata

Field	Value
Publication number	US-2021032216-A1
Application number	US-201916965746-A
Country	US
Kind code	A1
Filing date	Jan 31, 2019
Priority date	Jan 31, 2018
Publication date	Feb 4, 2021
Grant date	—

Abstract

A process for the conversion of solid lignocellulosic material containing hemicellulose, cellulose and lignin, includes (a) hydrolyzing, at a temperature equal to or less than 40° C. at least part of the hemicellulose and at least part of the cellulose of the solid lignocellulosic material with an aqueous hydrochloric acid solution, containing in the range from equal to or more than 40.0 wt. % to equal to or less than 51.0 wt. % hydrochloric acid, based on the combined weight amount of water and hydrochloric acid in the aqueous hydrochloric acid solution; yielding a hydrochloric acid-containing, aqueous hydrolysate solution; (b) separating the hydrochloric acid-containing, aqueous hydrolysate solution from the lignin; and (c) heating at least part of the hydrochloric acid-containing, aqueous hydrolysate solution to a temperature equal to or more than 60° C., yielding a product solution containing 5-(chloromethyl)furfural, and extracting the 5-(chloromethyl)furfural from the product solution into an extraction solvent.

First claim

1 . A process for the conversion of a solid lignocellulosic material containing hemicellulose, cellulose and lignin, the process including the following steps:
(a) hydrolyzing, at a temperature equal to or less than 40° C., preferably equal to or less than 30° C., at least part of the hemicellulose and at least part of the cellulose of the solid lignocellulosic material with an aqueous hydrochloric acid solution, containing in the range from equal to or more than 40.0 wt. % to equal to or less than 51.0 wt. % hydrochloric acid, based on the combined weight amount of water and hydrochloric acid in such aqueous hydrochloric acid solution; yielding a hydrochloric acid-containing, aqueous hydrolysate solution; (b) separating the hydrochloric acid-containing, aqueous hydrolysate solution from the lignin; and (c) heating at least part of the hydrochloric acid-containing, aqueous hydrolysate solution to a temperature equal to or more than 60° C., yielding a product solution containing 5-(chloromethyl)furfural, and extracting the 5-(chloromethyl)furfural from such product solution into an extraction solvent.

2 . The process according to claim 1 , wherein step (a) is carried out in a plurality of reactors, preferably connected in series:
wherein one or more portions of aqueous hydrochloric acid solution are moving from one reactor to another and are contacted with, optionally partially hydrolyzed, stationary lignocellulosic material in the reactors.

3 . The process according to claim 1 ,
wherein the aqueous hydrochloric acid solution is contacted counter-currently with the, optionally partially hydrolyzed, solid lignocellulosic material.

4 . The process according to claim 1 , wherein in step (a) one or more portions of aqueous hydrochloric acid solution form a plug or liquid column, optionally in combination with other fluids, which plug or liquid column is moving continuously or semi-continuously through a plurality of stationary reactors connected in series, each reactor containing an amount of, optionally already partially hydrolyzed, lignocellulosic material.

5 . The process according to claim 1 , wherein step (a) is carried out in a continuous or semi-continuous manner.

6 . The process according to claim 1 , wherein step (c) comprises heating at least part of the hydrochloric acid-containing, aqueous hydrolysate solution to a temperature equal to or more than 70° C., to thereby produce 5-(chloromethyl)furfural, and, in-situ, extracting at least part of the produced 5-(chloromethyl)furfural into an extraction solvent, to thereby produce a 5-(chloromethyl)furfural-containing extraction solvent.

7 . The process according to claim 6 , wherein step (c) is carried out in a biphasic counter-current flow reactor, where a flow of at least part of the hydrochloric acid-containing, aqueous hydrolysate solution is contacted counter-currently with a flow of extraction solvent.

8 . The process according to claim 6 , wherein the extraction solvent comprises toluene and/or 1,2-dichloroethane.

9 . The process according to claim 3 , wherein a, hydrochloric acid-containing, residual aqueous solution is obtained, and wherein such, hydrochloric acid-containing, residual aqueous solution is recycled to step (a), optionally after adjusting the hydrochloric acid concentration.

10 . The process according to claim 1 , wherein the process further comprises:
(i) isolating the 5-(chloromethyl)furfural from the extraction solvent and converting the isolated 5-(chloromethyl)furfural into 2,5 di-formylfuran, 5-(hydroxymethyl)furfural and/or 5-(alkoxymethyl)furfural; or (ii) retrieving the 5-(chloromethyl)furfural-containing extraction solvent and converting the 5-(chloromethyl)furfural, in the presence of the extraction solvent, into 2,5 di-formylfuran, 5-(hydroxymethyl)furfural and/or an 5-(alkoxymethyl)furfural.

11 . The process according to claim , comprising:
retrieving the 5-(chloromethyl)furfural-containing extraction solvent; and reacting the 5-(chloromethyl)furfural, in the presence of the extraction solvent, preferably at a temperature in the range from equal to or more than 10° C. to equal to or less than 90° C., more preferably equal to or less than 50° C., with an alkanol selected from the group consisting of ethanol, propanol, iso-propanol, butanol, iso-butanol and tert-butanol, yielding an 5-(alkoxymethyl)furfural.

12 . The process according to claim 1 , further comprising:
retrieving the 5-(chloromethyl)furfural-containing extraction solvent; and reacting the 5-(chloromethyl)furfural, in the presence of the extraction solvent, preferably at a temperature in the range from equal to or more than 10° C. to equal to or less than 90° C., more preferably equal to or less than 50° C., with methanol, yielding a 5-(methoxymethyl)furfural.

13 . The process according to claim 1 , further comprising:
retrieving the 5-(chloromethyl)furfural-containing extraction solvent; and reacting the 5-(chloromethyl)furfural, in the presence of the extraction solvent, preferably at a temperature in the range from equal to or more than 10° C. to equal to or less than 90° C., more preferably equal to or less than 50° C., with water, yielding a 5-(hydroxymethyl)furfural.

14 . The process according to claim 1 , further comprising:
retrieving the 5-(chloromethyl)furfural-containing extraction solvent; and oxydizing the 5-(chloromethyl)furfural, in the presence of the extraction solvent, to 2,5 di-formylfuran.

Assignees

• Furanix Technologies Bv

Inventors

• Van Putten Robert-Jan
• Mckay Benjamin
• Gruter Gerardus Johannes Maria
• Van Der Waal Jan Cornelis

Classifications

• C07D307/50 Primary

  Preparation from natural products · CPC title

• B01D2251/502

  Hydrochloric acid · CPC title

• B01D11/0284

  Multistage extraction · CPC title

• Y02E50/10

  Biofuels, e.g. bio-diesel · CPC title