Method for manufacturing structure
US-11459672-B2 · Oct 4, 2022 · US
US11390966B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11390966-B2 |
| Application number | US-201816235508-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 28, 2018 |
| Priority date | Dec 7, 2018 |
| Publication date | Jul 19, 2022 |
| Grant date | Jul 19, 2022 |
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Provided is a manufacturing method of a graphene-based liquid crystal fiber including: polymerizing a first aromatic monomer on a graphene-based compound to prepare a graphene composite in which a first aromatic polymer is surface-polymerized on the graphene-based compound; wet-spinning the graphene composite to manufacture a hydrogel fiber; and polymerizing a second aromatic monomer on the hydrogel fiber to fill pores of the hydrogel fiber with a second aromatic polymer.
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What is claimed is: 1. A manufacturing method of a graphene-based liquid crystal fiber comprising: (a) polymerizing a first aromatic monomer on a graphene-based compound to prepare a graphene composite in which a first aromatic polymer is surface-polymerized on the graphene-based compound; (b) wet-spinning the graphene composite to manufacture a hydrogel fiber; and (c) polymerizing a second aromatic monomer on the hydrogel fiber to fill pores of the hydrogel fiber with a second aromatic polymer, wherein the pores of the hydrogel fiber are filled by immersing, at 10° C. to 50° C. for 1 hour to 5 hours, the hydrogel fiber in a solution in which the second aromatic monomer is dissolved. 2. The manufacturing method of a graphene-based liquid crystal fiber of claim 1 , wherein a weight ratio of the graphene-based compound to the first aromatic monomer is 1:0.01 to 1:10. 3. The manufacturing method of a graphene-based liquid crystal fiber of claim 1 , wherein in a process of (a), the first aromatic polymer which is surface-polymerized on the graphene-based compound forms a surface layer with a thickness of 0.1 to 1 nm. 4. The manufacturing method of a graphene-based liquid crystal fiber of claim 1 , wherein in a process of (a), the surface polymerization of the first aromatic monomer is oxidation polymerization of the first aromatic monomer on a surface of the graphene-based compound. 5. The manufacturing method of graphene-based liquid crystal fiber of claim 1 , wherein a weight ratio of the graphene composite to the second aromatic monomer is 1:0.1 to 1:100. 6. The manufacturing method of graphene-based liquid crystal fiber of claim 1 , wherein the first aromatic monomer and the second aromatic monomer are a phenolic compound containing an amine group. 7. A manufacturing method of a graphene-based carbon fiber, comprising: (a) polymerizing a first aromatic monomer on a graphene-based compound to prepare a graphene composite in which a first aromatic polymer is surface-polymerized on the graphene-based compound; (b) wet-spinning the graphene composite to manufacture a hydrogel fiber; and (c) filling pores of the hydrogel fiber with a second aromatic polymer to manufacture a graphene-based liquid crystal fiber; and (d) carbonizing the graphene-based liquid crystal fiber, wherein the pores of the hydrogel fiber are filled by immersing, at 10° C. to 50° C. for 1 hour to 5 hours, the hydrogel fiber in a solution in which the second aromatic monomer is dissolved. 8. The manufacturing method of a graphene-based carbon fiber of claim 7 , wherein filling comprises polymerizing a second aromatic monomer on the hydrogel fiber to fill pores of the hydrogel fiber with the second aromatic polymer. 9. A graphene-based liquid crystal fiber comprising: a hydrogel fiber comprising a graphene-based compound modified with a first aromatic polymer and a second aromatic polymer filled in pores of the hydrogel fiber, wherein I D /I G of the graphene-based compound and the graphene-based compound modified with the first aromatic polymer satisfies the following Equation 1: ( I D /I G ) G /( I D /I G ) C >1 [Equation 1] wherein I D /I G is a measure of relative crystallinity which represents density of defects, and is calculated as a ratio of a maximum intensity value of a peak of an absorption region at 1350±10 cm −1 (I D ) to a maximum intensity value of a peak of an absorption region at 1590±10 cm −1 (I G ), in Raman spectroscopic analysis, (I D /I G ) G refers to I D /I G of the graphene-based compound, and (I D /I G ) C refers to I D /I G of a graphene composite modified with the first aromatic polymer, and wherein (I D /I G ) C of the graphene composite modified with the first aromatic polymer is 1 or less. 10. The graphene-based liquid crystal fiber of claim 9 , wherein the first aromatic monomer and the second aromatic monomer are a phenolic compound containing a nitrogen atom in a structural unit. 11. The graphene-based liquid crystal fiber of claim 9 , wherein adhesion of a graphene composite modified with the first aromatic polymer satisfies the following Equation 2: F C /F G >2 [Equation 2] wherein F G refers to adhesion between the graphene-based compounds, and F C refers to adhesion of the graphene composite modified with the first aromatic polymer. 12. A graphene-based carbon fiber comprising a graphene-based compound and graphitic nitrogen, having an electrical conductivity of 1×10 5 S/m or more and 1×10 6 S/m or less, wherein an inside of the graphene-based carbon fiber is formed of a dense texture which substantially does not include pores. 13. The graphene-based carbon fiber of claim 12 , wherein a tensile strength is 300 MPa or more. 14. The graphene-based carbon fiber of claim 12 , wherein the graphene-based carbon fiber contains 2 to 10 atom % of the graphitic nitrogen.
with only one nitrogen atom in the ring · CPC title
After-treatment · CPC title
Preparation of spinning solutions · CPC title
grafting · CPC title
from polyaddition, polycondensation or polymerisation products (D01F9/145, D01F9/16, D01F9/18 take precedence) · CPC title
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