Structured powder particles for feedstock improvement for laser based additive manufacturing
US-2017368603-A1 · Dec 28, 2017 · US
US2016199910A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016199910-A1 |
| Application number | US-201414915785-A |
| Country | US |
| Kind code | A1 |
| Filing date | Aug 18, 2014 |
| Priority date | Sep 2, 2013 |
| Publication date | Jul 14, 2016 |
| Grant date | — |
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A metal powder has a chromium content of at least 90 Ma %, a nanohardness according to EN ISO 14577-1 of ≦4 GPa and/or a green strength measured according to ASTM B312-09 of at least 7 MPa at a compression pressure of 550 MPa.
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1 - 23 . (canceled) 24 . A metal powder, comprising: a chromium content of at least 90 Ma %; and a nanohardness HIT 0.005/5/1/5 according to EN ISO 14577-1 of ≦4 GPa. 25 . A metal powder, comprising: a chromium content of at least 90 Ma %; and a green strength measured according to ASTM B312-09 of at least 7 MPa at a compression pressure of 550 MPa. 26 . The metal powder according to claim 24 , which further comprises a green strength measured according to ASTM B312-09 of at least 7 MPa at a compression pressure of 550 MPa. 27 . The metal powder according to claim 25 , which further comprises a nanohardness HIT 0.005/5/1/5 according to EN ISO 14577-1 of ≦4 GPa. 28 . The metal powder according to claim 24 , which further comprises a green strength measured according to ASTM B312-09 of at least 15 MPa at a compression pressure of 550 MPa. 29 . The metal powder according to claim 25 , which further comprises a green strength measured according to ASTM B312-09 of at least 15 MPa at a compression pressure of 550 MPa. 30 . The metal powder according to claim 24 , wherein the metal powder is chromium powder having a metallic purity ≧99.0 Ma %. 31 . The metal powder according to claim 25 , wherein the metal powder is chromium powder having a metallic purity ≧99.0 Ma %. 32 . The metal powder according to claim 24 , wherein the metal powder is an alloyed powder or composite powder. 33 . The metal powder according to claim 25 , wherein the metal powder is an alloyed powder or composite powder. 34 . The metal powder according to claim 24 , wherein the metal powder is granulated. 35 . The metal powder according to claim 25 , wherein the metal powder is granulated. 36 . The metal powder according to claim 24 , which further comprises a surface area according to BET of ≧0.05 m2/g with or without a surface-enlarging operation. 37 . The metal powder according to claim 25 , which further comprises a surface area according to BET of ≧0.05 m2/g with or without a surface-enlarging operation. 38 . The metal powder according to claim 24 , which further comprises a compression density at a compression pressure of 550 MPa being ≧80% of a theoretical density. 39 . The metal powder according to claim 25 , which further comprises a compression density at a compression pressure of 550 MPa being 80% of a theoretical density. 40 . A method for producing a metal powder, the method comprising the following steps: reducing at least one compound of the group consisting of chromium oxide and chromium hydroxide, optionally with an admixed solid carbon source, under at least temporary action of hydrogen and hydrocarbon to produce a metal powder having: a chromium content of at least 90 Ma %; and a nanohardness HIT 0.005/5/1/5 according to EN ISO 14577-1 of ≦4 GPa. 41 . A method for producing a metal powder, the method comprising the following steps: reducing at least one compound of the group consisting of chromium oxide and chromium hydroxide, optionally with an admixed solid carbon source, under at least temporary action of hydrogen and hydrocarbon to produce a metal powder having: a chromium content of at least 90 Ma %; and a green strength measured according to ASTM B312-09 of at least 7 MPa at a compression pressure of 550 MPa. 42 . The method according to claim 40 , which further comprises: heating the compound of the group consisting of chromium oxide and chromium hydroxide, optionally with an admixed solid carbon source, to a temperature TR with 1100° C.≦TR≦1550° C.; optionally holding the temperature at 1100° C.≦TR≦1550° C.; and at least temporarily setting the hydrocarbon partial pressure at 5 to 500 mbar at least during the heating step. 43 . The method according to claim 41 , which further comprises: heating the compound of the group consisting of chromium oxide and chromium hydroxide, optionally with an admixed solid carbon source, to a temperature TR with 1100° C.≦TR≦1550° C.; optionally holding the temperature at 1100° C.≦TR≦1550° C.; and at least temporarily setting the hydrocarbon partial pressure at 5 to 500 mbar at least during the heating step. 44 . The method according to claim 40 , wherein the action of hydrogen and hydrocarbon occurs at least in a temperature range of 800 to 1050° C. 45 . The method according to claim 41 , wherein the action of hydrogen and hydrocarbon occurs at least in a temperature range of 800 to 1050° C. 46 . The method according to claim 44 , which further comprises setting the hydrocarbon partial pressure at 5 to 500 mbar at least in the temperature range of 800 to 1050° C. 47 . The method according to claim 45 , which further comprises setting the hydrocarbon partial pressure at 5 to 500 mbar at least in the temperature range of 800 to 1050° C. 48 . The method according to claim 44 , which further comprises setting a sum of heating time and holding time in the temperature range of 800° C. to 1050° C. to be at least 45 minutes. 49 . The method according to claim 45 , which further comprises setting a sum of heating time and holding time in the temperature range of 800° C. to 1050° C. to be at least 45 minutes. 50 . The method according to claim 40 , which further comprises setting a total pressure at 0.95 to 2 bar. 51 . The method according to claim 41 , which further comprises setting a total pressure at 0.95 to 2 bar. 52 . The method according to claim 40 , which further comprises reducing the compound of the group consisting of chromium oxide and chromium hydroxide under at least temporary action of a H 2 —CH 4 gas mixture. 53 . The method according to claim 41 , which further comprises reducing the compound of the group consisting of chromium oxide and chromium hydroxide under at least temporary action of a H 2 —CH 4 gas mixture. 54 . The method according to claim 52 , which further comprises setting a H 2 /CH 4 volume ratio at 1 to 200 or 1.5 to 20. 55 . The method according to claim 53 , which further comprises setting a H 2 /CH 4 volume ratio at 1 to 200 or 1.5 to 20. 56 . The method according to claim 40 , which further comprises admixing a solid carbon source having at least one component selected from the group consisting of carbon black, activated carbon, graphite, carbon-releasing compound and mixtures thereof. 57 . The method according to claim 41 , which further comprises admixing a solid carbon source having at least one component selected from the group consisting of carbon black, activated carbon, graphite, carbon-releasing compound and mixtures thereof. 58 . The method according to claim 56 , which further comprises using between 0.75 and 1.25 mol or between 0.90 and 1.05 mol of carbon per mol of oxygen in the chromium oxide or chromium hydroxide. 59 . The method according to claim 57 , which further comprises using between 0.75 and 1.25 mol or between 0.90 and 1.05 mol of carbon per mol of oxygen in the chromium oxide or chromium hydroxide. 60 . The method according to claim 40 , which further comprises at least partially reacting at least one compound selected from the group consisting of chromium oxide and chromium hydroxide under the
Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties · CPC title
using gaseous reductors · CPC title
Hydrogen · CPC title
Alloys based on chromium · CPC title
Refractory metals · CPC title
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