IP Library › Granted Patent US 11,124,416
Granted Patent B2
US 11,124,416 · App. 16/320,710 · Granted Sep 21, 2021

Relating to graphene nanomaterials

Inventor: Richard John Price (Chester, GB)
Assignee: Kainos Innovation Limited
C01B32/194C01B32/184C01B2204/02C01B2204/04C01B2204/22C01B2204/24C01B2204/26C01P2002/82C01P2002/84C01P2002/85C01P2004/04C01P2004/51C01P2006/22
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Quick Facts
Patent No.
US 11,124,416
App. No.
16/320,710
Granted
Sep 21, 2021
Kind
B2
Abstract

A process for preparing a graphene nanomaterial product, the process comprising: cavitating a liquid medium comprising a diaromatic hydrocarbon component to synthesise from the diaromatic hydrocarbon component a dispersion of graphene nanomaterial in the liquid medium; and obtaining a graphene nanomaterial product from the dispersion.

Claims (23)

1. A process for preparing a functionalised graphene nanomaterial product, the process comprising:

cavitating a liquid medium comprising a diaromatic component and a functionalising component to synthesise functionalised graphene nanomaterial from the diaromatic component and the functionalising component and form a dispersion of the functionalised graphene nanomaterial in the liquid medium; and

obtaining a functionalised graphene nanomaterial product from the dispersion, wherein the functionalising component includes molecules comprising an amine group, molecules comprising a hydroxyl or peroxide group, molecules comprising a carboxylic acid group, or a combination thereof.

2. The process of claim 1 , wherein the nanomaterial product comprises graphene quantum dots, graphene nanoflakes, graphene nanoribbons, graphene nanosheets, or combinations thereof.

3. The process of claim 1 , comprising cavitating the liquid medium in the presence of oxygen or another heteroatom impurity and wherein the nanomaterial product comprises one or more heteroatom impurities.

4. The process of claim 1 , wherein the diaromatic component comprises optionally substituted fused or linked diaromatic hydrocarbons or heterocycles.

5. The process of claim 1 , wherein the diaromatic component is a diaromatic hydrocarbon component consisting of one or more optionally substituted diaromatic hydrocarbons.

6. The process of claim 1 , wherein the diaromatic component comprises one or more compounds of Formula A or Formula B, or heterocyclic variants thereof, optionally substituted with one or more moieties at one or more of the numbered positions:

7. The process of claim 6 , wherein the one or more moieties are selected from alkyl, alkenyl or alkynyl substituents, and halides.

8. The process of claim 6 , wherein the one or more moieties are selected from methyl, ethyl, and halides.

9. The process of claim 1 , wherein the diaromatic component comprises methylnaphthalene or ethylnaphthalene, and optionally naphthalene.

10. The process of claim 1 , wherein the liquid medium comprises a stabilising component for stabilising the dispersion of graphene nanomaterial to be formed.

11. The process of claim 10 , wherein the stabilising component comprises a solvent which on addition to the liquid medium, is capable of reducing the distance in Hansen space between the predicted Hansen Solubility Parameters of the liquid medium (HSPs: δ Ds , δ Ps and δ Hs ) and of graphene, graphene oxide, reduced graphene oxide, or functionalised graphene (HSPs: δ Dg , δ Pg and δ Hg ), such that it reduces R, where R 2 =(δ Dg −δ Ds ) 2 +(δ Pg −δ Ps ) 2 +(δ Hg −δ Hs ) 2 .

12. The process of claim 10 , wherein the stabilising component comprises N-Methyl-2-pyrrolidone (NMP).

13. The process of claim 10 , wherein the liquid medium consists of the diaromatic component, the functionalising component and a balancing amount of stabilising component.

14. The process of claim 1 , wherein the functionalising component is selected to enhance dispersion stability of the graphene nanomaterial.

15. The process of claim 1 , wherein the functionalising component comprises one or more compounds capable of taking part in a nucleophilic substitution, electrophilic substitution, condensation reaction or addition reaction.

16. The process of claim 1 , wherein the functionalising component comprises aromatic molecules, optionally substituted with one or more of an amine group, hydroxyl group, peroxide group, and carboxylic acid group.

17. The process of claim 1 , wherein the liquid medium comprises an emulsion of the functionalising component in the diaromatic component, the emulsion optionally being kinetically stable or thermodynamically stable.

18. The process of claim 1 wherein cavitation of the liquid is effected by subjecting the liquid medium to ultrasound.

19. A process for preparing a functionalised graphene nanomaterial product, the process comprising:

cavitating a liquid medium comprising a diaromatic component and a functionalising component to synthesise functionalised graphene nanomaterial from the diaromatic component and the functionalising component and form a dispersion of the functionalised graphene nanomaterial in the liquid medium; and

obtaining a functionalised graphene nanomaterial product from the dispersion, wherein the functionalising component is one or more compounds capable of taking part in a nucleophilic substitution, electrophilic substitution, condensation reaction or addition reaction and is present in an amount in the range of from 0.01 to 10% v/v based on the total volume of the liquid medium, and wherein the diaromatic component comprises methylnaphthalene or ethylnaphthalene, and optionally naphthalene.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 17, 2024
From: KAINOS INNOVATION LTD.
To: FIRST GRAPHENE LIMITED
Reel/Frame 067137/0027 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 25, 2019
From: PRICE, RICHARD JOHN
To: KAINOS INNOVATION LIMITED
Reel/Frame 048137/0841 →
Priority Claims (1)
GB 1613012 · Jul 27, 2016 · national
Continuity (1)
Related Publication 20190161352A1 · May 30, 2019