Method for manufacturing alloy powders based on titanium, zirconium and hafnium, alloyed with the elements Ni, Cu, Ta, W, Re, Os and Ir

Patent metadata

Field	Value
Publication number	US-9283622-B2
Application number	US-86750109-A
Country	US
Kind code	B2
Filing date	Feb 27, 2009
Priority date	Feb 28, 2008
Publication date	Mar 15, 2016
Grant date	Mar 15, 2016

Abstract

A method for manufacturing alloy powders based on titanium, zirconium and hafnium alloyed with the elements Ni, Cu, Ta, W, Re, Os, and Ir is described in which an oxide of Ti and Zr and Hf is mixed with a metal powder of the elements named and with a reducing agent, and wherein this mixture is heated in a furnace, optionally under a argonate atmosphere or, optionally under hydrogen atmosphere until the reducing reaction begins, the reaction product is leached and then washed and dried, wherein the oxide used has an average grain size of 0.5 to 20 μm, a specific surface area according to BET of 0.5 20 m 2 /g and a minimum content of 94 wet. −%. An easy to produce powder, in particular in relation to the ignition point and burning time, is produced.

First claim

It is claimed:

1. A method for producing an alloy powder comprising the steps of:
mixing at least one oxide selected from the group consisting of titanium oxide, zirconium oxide and hafnium oxide with at least one element selected from the group consisting of Ni, Cu, Ta, W, Re, Os and Ir, and a reducing agent to form a mixture;
heating the mixture in an oven in an argon atmosphere until a reduction reaction begins and a reaction product is obtained; and
leaching, washing and drying the reaction product to yield the alloy powder;
wherein the at least one oxide has a mean particle diameter (FSSS) of 0.5 to 20 μm, a BET specific surface area of 0.5 to 20 m 2 /g and a minimum metal oxide content of 94 wt. %; and
wherein the alloy powder has a burning time of 10 s/50 cm to 3000 s/50 cm, an ignition energy of 1 μJ to 10 mJ, an average particle size of from 1 to 8 μm, a BET specific surface area of 0.2 to 5 m 2 /g and an ignition temperature of 160° C. to 400° C.

2. A method as claimed in claim 1 , wherein the minimum metal oxide content is 99.5 wt. %.

3. A method as claimed in claim 1 , wherein the fraction of Si, Fe and Al impurities in the element is <0.1 wt. %.

4. A method as claimed in claim 1 , wherein the mixture in the oven is heated to 800 to 1400° C.

5. A method as claimed in claim 2 wherein the mixture in the oven is heated to 800 to 1400° C.

6. A method as claimed in claim 1 , wherein the fraction of Fe and Al impurities in the oxide is each <0.2 wt. %, calculated as the oxide.

7. A method as claimed in claim 6 , wherein the fraction of Fe and Al impurities in the oxide are each <0.1 wt. %, calculated as the oxide.

8. A method as claimed in claim 1 , wherein the fraction of Si impurities in the oxide is <1.5 wt. %, calculated as SiO 2 .

9. A method as claimed in claim 8 , wherein the fraction of SiO 2 impurities in the oxide is <0.3 wt. %, calculated as SiO 2 .

10. A method as claimed in claim 1 , wherein the fraction of Na impurities in the oxide is <0.05 wt. %, calculated as Na 2 O, and the fraction of P impurities in the oxide is <0.2 wt. %, calculated as P 2 O 5 .

11. A method as claimed in claim 1 , wherein the oxide used has an average particle size of 1 to 6 μm.

12. A method as claimed in claim 1 , wherein the oxide has a BET specific surface area of 1 to 12 m 2 /g.

13. A method as claimed in claim 1 , wherein the oxide has a BET specific surface area of 1 to 8 m 2 /g.

14. A method as claimed in claim 1 , wherein the oxide used has a minimum content of 96 wt. %.

15. A method as claimed in claim 1 , wherein the oxide has a minimum content of 99 wt. %.

16. A method as claimed in claim 1 , wherein the proportion of Na impurities in the oxide is<0.05 wt. % calculated as Na 2 O.

17. A method as claimed in claim 1 , wherein the proportion of P impurities in the oxide is <0.2 wt. % calculated as P 2 O 5 .

18. A method as claimed in claim 1 , wherein the ignition loss of the oxide at 1000° C. at constant weight is <1 wt. %.

19. A method as claimed in claim 1 , wherein the tamped density as defined in EN ISO 787-11 of the oxide is 800 to 1600 kg/m 3 .

20. A method as claimed in claim 1 , wherein the reducing agent is selected from the group consisting of an alkaline-earth metal, an alkali metal, an alkaline-earth hydride and an alkali metal hydride.

21. A method as claimed in claim 1 , wherein the reducing agent is selected from the group consisting of Mg, Ca, CaH 2 and Ba.

22. A method as claimed in claim 1 , wherein the reducing agent has a minimum content of reducing agent of 99 wt. %.

23. A method as claimed in claim 1 , wherein leaching of the reaction product is performed with hydrochloric acid.

24. A method as claimed in claim 1 , wherein the element is nickel.

25. A method as claimed in claim 24 wherein the argon atmosphere when heating the mixture of the reaction product with nickel powder is at a pressure of at least 100 hPa and wherein the mixture of the reaction product with nickel powder is heated at a temperature of between 500° C. to 1000° C.

26. A method for producing an alloy powder based on zirconium, alloyed with the element Ni, comprising mixing 36 kg of ZrO 2 having the following properties: ZrO 2 and HfO 2 minimum content of 98.5%, an HfO 2 content of from 1.0 to 2.0%, a SiO 2 maximum of 0.6%, a TiO 2 maximum content of 0.15%, an Fe 2 O 3 maximum content of 0.05%, an ignition loss maximum 0.5%, an average particle size (FSSS) 1.7 to 2.3 μm, together with 26.4 kg of calcium in the form of chips having the following properties: a Ca minimum content of 98.5%, a maximum Mg content of 0.5%, and 2.0 kg of magnesium in the form of chips having the following properties: a minimum Mg content of 99.5%, a bulk density maximum of 0.3 to 0.4 g/cm 3 in a mixing vessel for 20 minutes under an argon atmosphere;
introducing this mixture into a container, then sealing and filling the container with argon to an excess pressure of 100 hPa;
heating the mixture in an oven to a temperature of 1250° C. over one hour, wherein sixty minutes after the oven heating is switched on it is switched off again and, once the temperature has fallen to below 50° C. to react the mixture and form a reaction mass:
removing the resultant reaction mass is removed from the container; mixing the reaction mass with 13 kg of Ni powder having the following properties: a maximum C content of 0.1%, a maximum Fe content of 0.01%, a maximum O content of 0.15%, a maximum S content of 0.002%, an average particle size (FSSS) 4 to 6 μm, in a mixer for 30 minutes:
introducing the mixture into a container;
placing the container in an oven: sealing and filling the oven with argon to an excess pressure of 100 hPa;
heating the oven to temperatures of 500° C. to 1000° C. to form an alloy mixture, and thereafter removing the alloy mixture crucible:
leaching the removed alloy mixture with concentrated hydrochloric acid to form a leached mixture;
and then washing and drying the leached mixture to form the alloy powder; wherein the alloy powder has the following content analysis: 98.3% Zr and Ni, Zr 70.2%, Ni 28.1%, Hf 1.4%, Ca 0.09%, Fe 0.046%, Al 0.13%, S 0.003%, a burning time of 210 s/50 cm, an ignition temperature of 240° C., and an average particle size by FSSS of 4.21 μm.

27. A method for producing an alloy powder comprising the steps of:
mixing at least one oxide selected from the group consisting of titanium oxide, zirconium oxide with a reducing agent and heating the mixture in an oven having an argon atmosphere until a reduction reaction begins to obtain a reaction product;
cooling the reaction product;
mixing the cooled reaction product with an alloying metal selected from the group consisting of Ni, Cu, Ta, W, Re, Os and Ir to form an alloying mixture and heating the alloying mixture to form the alloy powder;
wherein the at least one oxide has a mean particle diameter (FSSS) of 0.5 to 20 μm, a BET specific surface area of 0.5 to 20 m 2 /g and a minimum metal content of 94 wt. %; and
wherein the alloy powder has a burning time of 10 s/50 cm to 3000 s/50 cm, an ignition energy of 1 μJ to 10 mJ, an average particle size of from 1 to 8 μm, a BET specific surface area of 0.2 to 5 m 2 /g and an ignition temperature of 160° C. to 400° C.

Assignees

• Karaca Ahmet
• Sermond Bernd
• Wilfing Gerhard
• Chemetall Gmbh

Inventors

• Karaca Ahmet
• Sermond Bernd
• Wilfing Gerhard

Classifications

• C22C1/0458

  Alloys based on titanium, zirconium or hafnium · CPC title

• C22C14/00

  Alloys based on titanium · CPC title

• C22C9/00

  Alloys based on copper · CPC title

• C01B6/24

  Hydrides containing at least two metals; Addition complexes thereof (C01B6/13 - C01B6/23 take precedence) · CPC title

• B22F9/20 Primary

  starting from solid metal compounds · CPC title