IP Library Granted Patent US 11,504,697
Granted Patent B2
US 11,504,697 · App. 16/335,340 · Granted Nov 22, 2022

Porous carbon material, method for producing same, and synthesis reaction catalyst

Inventors: Katsuya Tanba (Tokyo, JP); Yoshiharu Okuda (Tokyo, JP); Teiko Kuroda (Tokyo, JP)
Assignee: Dexerials Corporation
B01J21/18B01J23/44B01J35/10B01J35/1023B01J35/1028B01J35/1038B01J35/1042B01J35/1047B01J37/0215B01J37/0236B01J37/08B01J37/18C01B32/30C01B32/324C01B32/372C07C5/08C07C15/18C01P2002/72C01P2006/12C01P2006/14C07B61/00
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Quick Facts
Patent No.
US 11,504,697
App. No.
16/335,340
Granted
Nov 22, 2022
Kind
B2
Abstract

A porous carbon material, wherein a half width (2θ) of a diffraction peak (10×) (38° to 49°) by X-ray diffraction is 4.2° or less, and wherein a ratio (mesopore volume/micropore volume) of a mesopore volume (cm 3 /g) measured by a BJH method to a micropore volume (cm 3 /g) measured by a HK method is 1.20 or more.

Claims (26)

1. A porous carbon material,

wherein a half width (2θ) of a diffraction peak (10×) (38° to 49°) by X-ray diffraction is 4.2° or less, wherein 10× means a pseudo peak observed in the vicinity of the 101 plane in graphite, and

wherein a ratio (mesopore volume/micropore volume) of a mesopore volume (cm 3 /g) measured by a BJH method to a micropore volume (cm 3 /g) measured by a HK method is 1.20 or more, but 2.00 or less.

2. The porous carbon material according to claim 1 , wherein the porous carbon material is derived from a plant.

3. The porous carbon material according to claim 1 , wherein the porous carbon material is derived from chaff.

4. The porous carbon material according to claim 1 , wherein the porous carbon material is a carrier for a catalyst.

5. A method for producing the porous carbon material according to claim 1 , the method comprising:

removing, from a raw material containing a silicon component, the silicon component by an acid treatment or an alkali treatment, and then performing a carbonization treatment.

6. The method for producing the porous carbon material according to claim 5 , wherein an activation treatment is performed after the carbonization treatment.

7. The method for producing the porous carbon material according to claim 6 , wherein a heat treatment is performed after the activation treatment.

8. The method for producing the porous carbon material according to claim 7 , wherein a temperature of the heat treatment is 1,200° C. or higher.

9. The method for producing the porous carbon material according to claim 5 , wherein a temperature of the carbonization treatment is 600° C. or higher.

10. A method for producing the porous carbon material according to claim 1 , the method comprising:

performing a carbonization treatment on a raw material containing a silicon component, then removing the silicon component from an obtained carbonized product by an acid treatment or an alkali treatment, and then performing an activation treatment.

11. The method for producing the porous carbon material according to claim 10 , wherein a heat treatment is performed after the activation treatment.

12. The method for producing the porous carbon material according to claim 11 , wherein a temperature of the heat treatment is 1,200° C. or higher.

13. The method for producing the porous carbon material according to claim 10 , wherein a temperature of the carbonization treatment is 600° C. or higher.

14. A synthesis reaction catalyst comprising:

the porous carbon material according to claim 1 ; and

a metal or a metal compound carried on the porous carbon material.

15. The synthesis reaction catalyst according to claim 14 , wherein the metal or the metal compound palladium.

16. A porous carbon material,

wherein the porous carbon material is subjected to heat treatment at a temperature of 1,200° C. or higher,

wherein the porous carbon material exhibits the following properties after heat treatment:

(a) a half width (2θ) of a diffraction peak (10×) (38° to 49°) by X-ray diffraction is 4.2° or less, wherein 10× means a pseudo peak observed in the vicinity of the 101 plane graphite, and

(b) a ratio (mesopore volume/micropore volume) of a mesopore volume (cm 3 /g) measured by a Bill method to a micropore volume (cm 3 /g) measured by a HK method is 1.20 or more, but 2.00 or less.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 21, 2019
From: TANBA, KATSUYA; OKUDA, YOSHIHARU; KURODA, TEIKO
To: DEXERIALS CORPORATION
Reel/Frame 048663/0756 →
Priority Claims (1)
JP JP2016-187106 · Sep 26, 2016 · national
Continuity (1)
Related Publication 20190275498A1 · Sep 12, 2019