Device for the electronic and electrochemical measurement of analyte concentrations in biological samples
US-2024219386-A1 · Jul 4, 2024 · US
US10458046B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10458046-B2 |
| Application number | US-201815898762-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 19, 2018 |
| Priority date | Mar 15, 2011 |
| Publication date | Oct 29, 2019 |
| Grant date | Oct 29, 2019 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention relates to a graphene conjugate fiber and a method for manufacturing same, and more particularly, to a conjugate fiber including graphene and a polymer, wherein a wrinkled structure of the graphene is maintained in a fiber state. The graphene conjugate fiber manufactured thereby has superior mechanical properties, is flexible, and has high utility by being manufactured as a fiber.
Opening claim text (preview).
The invention claimed is: 1. A method for producing a graphene composite fiber, the method comprising: a) dispersing graphene and a surfactant in a solvent to prepare a dispersion, b) spinning the dispersion into a coagulation bath containing polymer solution to form a graphene-gel fiber, and c) drying the graphene-gel fiber to produce the graphene composite fiber. 2. The method according to claim 1 , further comprising d) annealing the graphene composite fiber obtained in c) at a temperature of 140 to 160° C. 3. The method according to claim 1 , further comprising d′) dipping the graphene composite fiber obtained in c) in methanol or acetone to improve the degree of crystallization of the graphene composite fiber. 4. The method according to claim 1 , wherein the graphene is chemically reduced graphene. 5. The method according to claim 1 , wherein the graphene is chemically reduced graphene with acid functional groups. 6. The method according to claim 5 , wherein the chemically reduced graphene is prepared by reducing an aqueous dispersion of graphene with hydrazine at 90 to 100° C. for 1 to 24 hours. 7. The method according to claim 1 , wherein the surfactant is selected from sodium dodecyl benzene sulfonate (SDBS), sodium dodecyl sulfonate (SDS), Triton X-100, and cetyltrimethylammonium bromide (CTAB). 8. The method according to claim 1 , wherein the solvent is water. 9. The method according to claim 1 , wherein, in the coagulation bath, the polymer from the polymer solution is incorporated into the spun dispersion to form the graphene-gel fiber in which the graphene is surrounded by the polymer. 10. The method according to claim 1 , wherein, during drying, the graphene gel-fiber is vertically suspended and dried. 11. The method according to claim 1 , wherein the graphene is a graphene flake.
from polymers of unsaturated alcohols, e.g. polyvinyl alcohol, or of their acetals or ketals · CPC title
Preparation of spinning solutions · CPC title
Heat treatment (heating for finishing D02J13/00) · CPC title
Other agents for modifying properties · CPC title
including free carbon or carbide or therewith [not as steel] · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.