Three-dimensional multi-reinforced composites and methods of manufacture and use thereof
US-2016176156-A1 · Jun 23, 2016 · US
US10214455B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10214455-B2 |
| Application number | US-201715492628-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 20, 2017 |
| Priority date | Apr 21, 2016 |
| Publication date | Feb 26, 2019 |
| Grant date | Feb 26, 2019 |
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Provided herein are methods of making composite materials. The methods may include infiltrating a carbon nanoscale fiber network with a ceramic precursor, curing the ceramic precursor, and/or pyrolyzing the ceramic precursor. The infiltrating, curing, and pyrolyzing steps may be repeated one or more times. Composite materials also are provided that include a ceramic material and carbon nanoscale fibers.
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I claim: 1. A method of forming a composite material, the method comprising: providing a carbon nanoscale fiber network which comprises a plurality of substantially aligned carbon nanoscale fibers; infiltrating the carbon nanoscale fiber network with a first amount of a liquid ceramic precursor; curing the first amount of the liquid ceramic precursor to form a cured ceramic precursor; and pyrolyzing the cured ceramic precursor to form the composite material; wherein the composite material comprises the carbon nanoscale fibers at a volume fraction of at least 35%. 2. The method of claim 1 , wherein the volume fraction of the carbon nanoscale fibers in the composite material is about 40% to about 80%. 3. The method of claim 1 , wherein the electrical conductivity of the composite material is about 2.0×10 4 S/m to about 3.0×10 4 S/m. 4. The method of claim 1 , further comprising: infiltrating a second amount of the liquid ceramic precursor into the composite material; curing the second amount of the liquid ceramic precursor to form a second amount of a cured ceramic precursor; and pyrolyzing the second amount of the cured ceramic precursor. 5. The method of claim 4 , wherein the volume fraction of carbon nanoscale fibers in the composite material is about 50% to about 70%. 6. The method of claim 4 , wherein the electrical conductivity of the composite material is about 2.0×10 4 S/m to about 2.5×10 4 S/m. 7. The method of claim 4 , wherein the composite material is (i) flexible, and (ii) has a tensile strength of at least 400 MPa. 8. The method of claim 1 , wherein the providing of the carbon nanoscale fiber network comprises: providing a carbon nanoscale fiber network which comprises a plurality of randomly oriented carbon nanoscale fibers; and stretching the carbon nanoscale fiber network to substantially align the plurality of randomly oriented carbon nanoscale fibers, wherein the stretching of the carbon nanoscale fiber network imparts the carbon nanoscale fiber network with a stretch ratio of about 10% to about 70%. 9. The method of claim 8 , wherein the stretch ratio is about 25% to about 45%. 10. The method of claim 8 , wherein the stretch ratio is about 35%. 11. The method of claim 1 , wherein the plurality of substantially aligned carbon nanoscale fibers comprises single-wall carbon nanotubes, multi-wall carbon nanotubes, or a combination thereof. 12. The method of claim 1 , wherein the liquid ceramic precursor comprises a polysilazane, a polysiloxane, a polyborosiloxane, a polyborosilane, a polyborosilazane, a polycarbosiloxane, a polycarbosilane, or a combination thereof.
Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance · CPC title
Orientation of the fibers · CPC title
by wet chemical techniques · CPC title
Carbon nanotubes · CPC title
with more than one coating layer · CPC title
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