US2014360493A1PendingUtilityA1
Process for the conversion of cellulose in hydrated molten salts
Est. expiryOct 9, 2027(~1.2 yrs left)· nominal 20-yr term from priority
C07C 29/132C13K 1/02C07H 1/00C08B 1/003C07H 3/02
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Claims
Abstract
A process for converting cellulose to glucose, said process comprising the steps of: providing a hydrated molten salt; contacting the hydrated molten salt with a cellulose-containing material to form dissolved glucose; removing the dissolved glucose from the hydrated molten salt.
Claims
exact text as granted — not AI-modified1 . A process for converting cellulose to glucose, said process comprising the steps of:
a) providing a hydrated molten salt; b) contacting the hydrated molten salt with a cellulose-containing material to form dissolved glucose; c) removing the dissolved glucose from the hydrated molten salt.
2 . The process of claim 1 wherein the cellulose-containing material is a cellulosic biomass.
3 . The process of claim 1 or 2 wherein step c) comprises selectively adsorbing cellulose to Sephadex.
4 . The process of claim 1 or 2 wherein step c) comprises flushing the hydrated molten salt with a solvent.
5 . The process of claim 4 wherein the solvent is selected from the group consisting of organic solvents, supercritical fluids, and mixtures thereof.
6 . The process of claim 1 or 2 wherein the dissolved glucose is removed by conversion to a material that is poorly soluble in the hydrated molten salt.
7 . The process of claim 6 wherein the glucose is converted to a material comprising an alcohol.
8 . The process of claim 7 wherein the glucose is converted to a material comprising an alcohol by a process comprising mild hydrogenation.
9 . The process of claim 7 wherein the glucose is converted to a material comprising an alcohol by a process comprising selective oxidation.
10 . The process of any one of claims 6 - 9 wherein the conversion is carried out electrochemically.
11 . The process of any one of claims 6 - 9 wherein the conversion is carried out under the addition of microwave energy.
12 . The process of any one of claims 6 - 9 wherein the conversion is carried out under the addition of ultrasound energy.
13 . The process of any one of claims 6 - 9 wherein the conversion is catalyzed in the presence of a catalyst.
14 . The process of claim 13 wherein the catalyst is a particulate solid material that is dispersed in the hydrated molten salt.
15 . The process of any one of claims 7 - 14 comprising the further step of hydrogenating the alcohol to form an alkane.
16 . The process of claim 15 wherein the alcohol is separated from the hydrated molten salt prior to conversion to the alkane.
17 . The process of claim 2 wherein the cellulosic biomass is substantially lignin-free.
18 . The process of claim 17 wherein the substantially lignin-free biomass is prepared by mild hydrothermal treatment of lignin-containing biomass.
19 . The process of any of claims 6 - 18 wherein the conversion comprises a reaction is a micro channel reactor.
20 . The process of claim 19 wherein the micro channel reactor is at least partially coated with a catalytic material.
21 . The process of claim 15 or 16 wherein hydrogen used in the hydrogenation reaction is generated by reforming cellulosic biomass.
22 . The process of claim 15 or 16 wherein hydrogen used in the hydrogenation reaction is generated by reforming lignin.
23 . A process for selectively dissolving cellulose, said process comprising the steps of:
a. Providing a source of lignocellulosic material; b. Contacting the lignocellulosic material with a molten salt under reaction conditions that minimize the depolymerization of cellulose.
24 . The process of claim 23 wherein the lignocellulosic material further comprises hemicellulose.
25 . The process of claim 24 wherein the lignocellulosic material is a lignocellulosic biomass material.
26 . The process of any one of the preceding claims wherein the hydrated molten salt is hydrated zinc chloride.
27 . The process of any one of claims 23 - 26 wherein the reaction conditions comprise a temperature of from 40 to 80° C.
28 . The process of claim 27 wherein the reaction conditions comprise the substantial absence of mineral acid.
29 . The process of any one of claims 23 - 28 whereby water is removed from the molten salt during step b).
30 . The process of claim 29 whereby step b) is carried out under reduced pressure.
31 . The process of claim 30 whereby step b) is carried out at a pressure which is at or near the saturated steam pressure of the reaction temperature.
32 . The process of claim 31 whereby step b) is carried out at a temperature in the range of 60 to 70° C. and a pressure in the range of 0.20 to 0.30 bar.
33 . The process of any one of claims 23 - 32 whereby lignin is removed from the molten salt during or after step b).
34 . The process of any one of claims 24 - 33 whereby hemicellulose is converted to a reaction product comprising an alcohol.
35 . The process of claim 34 wherein the reaction product comprises xylotol.
36 . The process of any one of claims 23 - 35 wherein the solution obtained in step b) is extruded into a coagulating medium.
37 . The process of claim 36 wherein the coagulating medium is selected from the group consisting of the C 1 to C 8 alcohols, the C 1 to C 8 ketones, and mixtures thereof.
38 . The process of claim 36 or 37 wherein the cellulose is extruded in the form of fibers.
39 . The process of claim 38 wherein the cellulose fibers are subjected a post-treatment step for increasing the crystallinity of the cellulose.
40 . The process of claim 39 wherein the post-treatment step comprises stretching.Join the waitlist — get patent alerts
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