IP Library Granted Patent US 12680038
Granted Patent B2
US 12680038 · App. 18/154,146 · Granted Jul 14, 2026

Method for gasifying biomass

Inventors: Thierry Chataing (Grenoble, FR); Gilles Ratel (Grenoble, FR); Thomas Robin (Toulon, FR)
Assignee: COMMISSARIAT À L'ÉNERGIE ATOMIQUE ET AUX ÉNERGIES ALTERNATIVES
C10J3/12C10J2200/09C10J2200/158C10J2200/36C10J2300/092C10J2300/0923
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12680038
App. No.
18/154,146
Granted
Jul 14, 2026
Kind
B2
Abstract

Gasification method comprising the following steps of: a) bringing, in a main reactor, beads made of steel, an alloy, glass or ceramic, at a temperature between 600° C. and 1,000° C., into contact with a feedstock mixture comprising water and a biomass, the biomass comprising an organic part and salts, the main reactor being pressurised to more than 224 bar and at a temperature above 200° C. b) gasifying the organic part in the presence of the beads, thereby forming a gaseous phase, an aqueous phase and a solid residue, and whereby the salts precipitate on the beads, forming a salt shell covering the beads, c) separating the beads from the organic part, d) regenerating the beads.

Claims (23)

1 . A method for gasifying biomass comprising the steps of:

a) in a main reactor, bringing beads that have been pre-heated to a temperature between 600° C. and 1,000° C. into contact with a feedstock mixture comprising water and a biomass, the biomass comprising an organic part and salts,

wherein the beads are made of a material that is selected from steel, a metal alloy, glass or a ceramic,

and wherein the main reactor is pressurised to more than 222 bar;

b) at least partially gasifying the organic part, in the presence of the beads at a temperature above 374° C. and at a pressure above 222 bar, thereby forming a gaseous phase, an aqueous phase and a solid residue, and whereby the salts precipitate on the beads, forming a salt shell covering the beads;

c) separating the beads covered by the salt shell from any recoverable organic part; and

d) regenerating the beads.

2 . The method according to claim 1 , wherein in step a), the main reactor is heated to a temperature above 200° C. and below 374° C.

3 . The method according to claim 1 , wherein step d) comprises the following sub-steps:

d1) removing the salt shell of the beads; and

d2) pre-heating the beads to a temperature between 600° C. and 1,000° C.

4 . The method according to claim 3 , wherein step d1) is carried out by washing the beads with an aqueous solution at a temperature below 374° C., whereby the salts are dissolved.

5 . The method according to claim 3 , wherein sub-step d2) is carried out in a heating reactor positioned between a collection chamber and the main reactor.

6 . The method according to claim 3 , wherein during sub-step d1), the beads are washed with the aqueous phase from step b).

7 . The method according to claim 3 , wherein the solid residue from step b) is used to pre-heat the beads to a temperature between 600° C. and 1,000° C. in sub-step d2).

8 . The method according to claim 1 , wherein the biomass has a moisture content of over 50%, whereby the biomass can be ground prior to step a).

9 . The method according to claim 8 , wherein the biomass comprises microalgae, macroalgae, agricultural waste, household waste, sludge from wastewater treatment plants or wastewater.

10 . The method according to claim 1 , wherein the beads have a diameter of from 500 μm to 2 mm.

11 . The method according to claim 1 , wherein the method further comprises a step in which oils contained in the biomass are dissolved by injecting ethanol into the main reactor.

12 . The method according to claim 1 , wherein the method further comprises a subsequent step e) in which a further gasification step is carried out at a pressure above 222 bar in order to gasify the organic part not gasified in step b), the temperature in step e) being between 60° and 700° C. or step e) being carried out in the presence of a catalyst at a temperature below 500° C.

13 . The method according to claim 1 , wherein, in step b), the organic part is gasified in a gasification reactor.

14 . The method according to claim 13 , wherein the gasification reactor is in fluid communication with a collection chamber and in that, in step c), the beads are collected in the collection chamber.

15 . The method according to claim 1 , wherein the feedstock mixture is preheated to a temperature from 150° C. to 250° C., before step a).