Systems and methods for producing a carbon composite material
US-2016376203-A1 · Dec 29, 2016 · US
US11131503B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11131503-B2 |
| Application number | US-201815936025-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 26, 2018 |
| Priority date | Mar 26, 2018 |
| Publication date | Sep 28, 2021 |
| Grant date | Sep 28, 2021 |
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A method of manufacture for a carbon/carbon part including a method to remove contamination from an intermediate product of the carbon/carbon part and furnace utilizing a gaseous reducing agent hydrogen gas to reduce the contaminates, thereby causing the contaminates to transition to a gaseous state at relatively lower temperatures. A method to remove contamination from an intermediate product of the carbon/carbon part and furnace utilizing hydrogen gas to reduce the contaminates, thereby causing the contaminates to transition to a gaseous state at relatively lower temperatures.
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What is claimed is: 1. A method of manufacturing a carbon/carbon brake disk comprising: forming a carbon preform; placing the carbon preform within a furnace; purifying the carbon preform by: introducing a gaseous reducing agent into the furnace at a first temperature; increasing a temperature within the furnace to a second temperature greater than the first temperature; removing the gaseous reducing agent from the furnace by at least one of creating a first pressure differential or flowing a first purging gas through the furnace; increasing the temperature within the furnace to a third temperature greater than the second temperature and decreasing a pressure within the furnace, after removing the gaseous reducing agent, to vaporize a contaminate; and removing the vaporized contaminate from the furnace by at least one of creating a second pressure differential or flowing a second purging gas through the furnace; and carbonizing the carbon preform after purifying the carbon preform. 2. The method of claim 1 , further comprising densifying the carbon preform after carbonizing the carbon preform. 3. The method of claim 1 , wherein removing the gaseous reducing agent from the furnace comprises flowing the first purging gas through the furnace, and wherein the first purging gas is at least one of argon, helium, krypton, neon, xenon, or nitrogen. 4. The method of claim 3 , wherein the gaseous reducing agent is hydrogen gas. 5. The method of claim 4 , wherein the furnace is at a first pressure between 0.5 kPa and 31 kPa when the hydrogen gas is introduced, and wherein the furnace is at a second pressure greater than the first pressure when the furnace is at the second temperature. 6. The method of claim 5 , wherein the second pressure is between 13 kPa and 400 kPa. 7. The method of claim 6 , wherein the furnace is held at the second temperature for a reduction time. 8. The method of claim 6 , wherein the first temperature is between 0° C. and 40° C., and wherein the second temperature is between 500° C. and 900° C., and wherein the third temperature is between 1700° C. and 2400° C. 9. The method of claim 1 , further comprising flowing a pre-reduction purging gas through the furnace prior to introducing the gaseous reducing agent, wherein the pre-reduction purging gas is an inert gas. 10. The method of claim 9 , wherein the pre-reduction purging gas is at least one of argon, helium, krypton, neon, xenon, or nitrogen gas. 11. The method of claim 1 , wherein the vaporized contaminate comprises at least one of sodium, potassium, calcium, iron, nickel, titanium and silicon. 12. The method of claim 1 , wherein the pressure within the furnace is decreased to between 0.5 Pa and 15.0 Pa to vaporize the contaminate.
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