EP1043411A2 - Verfahren zur Herstellung von metallischem Verbundmaterial - Google Patents
Verfahren zur Herstellung von metallischem Verbundmaterial Download PDFInfo
- Publication number
- EP1043411A2 EP1043411A2 EP00105246A EP00105246A EP1043411A2 EP 1043411 A2 EP1043411 A2 EP 1043411A2 EP 00105246 A EP00105246 A EP 00105246A EP 00105246 A EP00105246 A EP 00105246A EP 1043411 A2 EP1043411 A2 EP 1043411A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- solution
- powder
- water
- hard constituent
- metal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
- C22C1/04—Making non-ferrous alloys by powder metallurgy
- C22C1/05—Mixtures of metal powder with non-metallic powder
- C22C1/051—Making hard metals based on borides, carbides, nitrides, oxides or silicides; Preparation of the powder mixture used as the starting material therefor
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C29/00—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides
- C22C29/02—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides
- C22C29/06—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds
- C22C29/08—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds based on tungsten carbide
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2999/00—Aspects linked to processes or compositions used in powder metallurgy
Definitions
- the present invention relates to a method of producing metal composite materials such as cemented carbide.
- Hard constituent powder and, optionally, a soluble carbon source are added to the solution.
- the solvent is evaporated and remaining powder is heat-treated in inert and/or reducing atmosphere.
- hard constituent powder coated with at least one iron group metal is obtained which after addition of pressing agent can be compacted and sintered according to standard practice to a body containing hard constituents in a binder phase.
- grain growth inhibitors When making submicron cemented carbide i.e. with a WC grain size of ⁇ 1 ⁇ m grain growth inhibitors have to be added in order to avoid WC grain growth during sintering.
- grain growth inhibitors the metals V and Cr are often used but also Mo and W can be used.
- the powder obtained was fired in a furnace in a porous bed about 1 cm thick in nitrogen atmosphere in a closed vessel, heating rate 10°C/min to 500°C, completed with reduction in hydrogen for 90 minutes, finally followed by cooling in nitrogen atmosphere at 10°C/min. No cooling step between burning off and reduction step was used.
- the powder obtained was mixed with pressing agent in ethanol with adjustment of carbon content (carbon black), dried, compacted and sintered according standard practice for WC-Co alloys.
- Example 2 A WC-0.9 wt%Mo-10 wt%Co cemented carbide was made in the same way as in Example 1 but with no addition of cobalt acetate tetrahydrate (Co(C 2 H 3 O 2 ) 2 x 4H 2 O) and only 1.7 g triethanolamine to the solution. The same result as in Example 1 was obtained.
- a WC-0.9 wt%Mo-10 wt%Co cemented carbide was made in the same way as in Example 1 but the solution used was a mixture of 250 ml methanol + 100 ml water (1.06 g ammonium molybdate tetrahydrate/100 ml solution). The same result as in Example 1 was obtained.
- a WC-0.9 wt%Mo-10 wt%Co cemented carbide was made in the same way as in Example 1 but the solution used was a mixture of 100 ml ethanol + 140 ml water (1.54 g ammonium molybdate tetrahydrate/100 ml solution). The same result as in Example 1 was obtained.
- a WC-0.9 wt%Mo-10 wt%Co cemented carbide was made in the same way as in Example 1 but the solution used was a mixture of 230 ml ethanol + 20 ml water (1.48 g ammonium molybdate tetrahydrate/100 ml solution). A cemented carbide structure with porosity A02, B04 was obtained.
- the powder obtained was fired in a furnace in a porous bed about 1 cm thick in nitrogen atmosphere in a closed vessel, heating rate 10°C/min to 500°C, completed with reduction in hydrogen for 90 minutes, finally followed by cooling in nitrogen atmosphere at 10°C/min. No cooling step between burning off and reduction step was used.
- the powder obtained was mixed with pressing agent in ethanol with adjustment of carbon content (carbon black), dried, compacted and sintered according standard practice for WC-Co alloys.
- a WC-0.9 wt%W-10 wt%Co cemented carbide was made in the same way as in Example 6 but with no addition of cobalt acetate tetrahydrate (Co(C 2 H 3 O 2 ) 2 x 4H 2 O) and only 1.0 g triethanolamine to the solution. The same result as in Example 6 was obtained.
- a WC-0.9 wt%W-10 wt%Co cemented carbide was made in the same way as in Example 6 but the solution used was a mixture of 175 ml methanol + 175 ml water (0.83 g ammonium metatungstate hydrate/100 ml solution). The same result as in Example 6 was obtained.
- a WC-0.9 wt%W-10 wt%Co cemented carbide was made in the same way as in Example 6 but the solution used was a mixture of 200 ml ethanol + 100 ml water (0.97 g ammonium metatungstate hydrate/100 ml solution). The same result as in Example 6 was obtained.
- a WC-0.9 wt%W-10 wt%Co cemented carbide was made in the same way as in Example 6 but the solution used was 200 ml ethanol with no water (1.45 g ammonium metatungstate hydrate/100 ml solution).
- a cemented carbide structure with high porosity A04, B08 was obtained.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Powder Metallurgy (AREA)
- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
- Manufacture Of Alloys Or Alloy Compounds (AREA)
- Carbon And Carbon Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE9901206A SE519233C2 (sv) | 1999-04-06 | 1999-04-06 | Sätt att tillverka metallkompositmaterial för hårdmetall |
SE9901206 | 1999-04-06 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP1043411A2 true EP1043411A2 (de) | 2000-10-11 |
EP1043411A3 EP1043411A3 (de) | 2005-11-02 |
EP1043411B1 EP1043411B1 (de) | 2008-07-09 |
Family
ID=20415101
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP00105246A Expired - Lifetime EP1043411B1 (de) | 1999-04-06 | 2000-03-14 | Verfahren zur Herstellung von metallischem Verbundmaterial |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP1043411B1 (de) |
JP (1) | JP2000313929A (de) |
AT (1) | ATE400669T1 (de) |
DE (1) | DE60039384D1 (de) |
SE (1) | SE519233C2 (de) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2678514A4 (de) * | 2011-02-22 | 2017-01-11 | Baker Hughes Incorporated | Verfahren zur herstellung polykristalliner presslinge, schneideelemente und erdbohrwerkzeuge |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102187005A (zh) | 2008-10-20 | 2011-09-14 | H.C.施塔克股份有限公司 | 用于生产基于碳化钨的硬质金属的含钼金属粉末 |
DE102008052559A1 (de) | 2008-10-21 | 2010-06-02 | H.C. Starck Gmbh | Metallpulver |
JP6228765B2 (ja) * | 2013-06-19 | 2017-11-08 | 小林 博 | ナノ粒子の製造方法 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0916743A1 (de) * | 1997-10-14 | 1999-05-19 | Sandvik Aktiebolag | Verfahren zur Herstellung von Metallverbundwerkstoffen |
-
1999
- 1999-04-06 SE SE9901206A patent/SE519233C2/sv not_active IP Right Cessation
-
2000
- 2000-03-14 EP EP00105246A patent/EP1043411B1/de not_active Expired - Lifetime
- 2000-03-14 DE DE60039384T patent/DE60039384D1/de not_active Expired - Fee Related
- 2000-03-14 AT AT00105246T patent/ATE400669T1/de not_active IP Right Cessation
- 2000-04-05 JP JP2000108002A patent/JP2000313929A/ja active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0916743A1 (de) * | 1997-10-14 | 1999-05-19 | Sandvik Aktiebolag | Verfahren zur Herstellung von Metallverbundwerkstoffen |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2678514A4 (de) * | 2011-02-22 | 2017-01-11 | Baker Hughes Incorporated | Verfahren zur herstellung polykristalliner presslinge, schneideelemente und erdbohrwerkzeuge |
US10647614B2 (en) | 2011-02-22 | 2020-05-12 | Baker Hughes Incorporated | Cutting elements and tools comprising interbonded grains of diamond and related compositions |
US10766823B2 (en) | 2011-02-22 | 2020-09-08 | Baker Hughes, A Ge Company, Llc | Cutting elements and tools comprising interbonded grains of diamond and related methods |
Also Published As
Publication number | Publication date |
---|---|
EP1043411A3 (de) | 2005-11-02 |
SE9901206L (sv) | 2000-10-07 |
ATE400669T1 (de) | 2008-07-15 |
JP2000313929A (ja) | 2000-11-14 |
SE519233C2 (sv) | 2003-02-04 |
SE9901206D0 (sv) | 1999-04-06 |
DE60039384D1 (de) | 2008-08-21 |
EP1043411B1 (de) | 2008-07-09 |
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