US20050118053A1 - Process for complex transient liquid phase sintering of powder metal - Google Patents
Process for complex transient liquid phase sintering of powder metal Download PDFInfo
- Publication number
- US20050118053A1 US20050118053A1 US10/724,248 US72424803A US2005118053A1 US 20050118053 A1 US20050118053 A1 US 20050118053A1 US 72424803 A US72424803 A US 72424803A US 2005118053 A1 US2005118053 A1 US 2005118053A1
- Authority
- US
- United States
- Prior art keywords
- liquid phase
- set forth
- mixture
- lubricant
- sintering
- 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.)
- Abandoned
Links
- 239000007791 liquid phase Substances 0.000 title claims abstract description 52
- 239000000843 powder Substances 0.000 title claims abstract description 50
- 238000005245 sintering Methods 0.000 title claims abstract description 36
- 238000000034 method Methods 0.000 title claims abstract description 35
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 34
- 239000002184 metal Substances 0.000 title claims abstract description 34
- 230000001052 transient effect Effects 0.000 title description 3
- 239000000203 mixture Substances 0.000 claims abstract description 42
- 239000000314 lubricant Substances 0.000 claims abstract description 33
- 239000007788 liquid Substances 0.000 claims abstract description 11
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910000851 Alloy steel Inorganic materials 0.000 claims abstract description 6
- 238000001704 evaporation Methods 0.000 claims abstract description 3
- 229910052742 iron Inorganic materials 0.000 claims abstract description 3
- 238000009827 uniform distribution Methods 0.000 claims abstract description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 27
- 239000002245 particle Substances 0.000 claims description 20
- 239000000047 product Substances 0.000 claims description 17
- 229910021383 artificial graphite Inorganic materials 0.000 claims description 13
- 238000005056 compaction Methods 0.000 claims description 13
- 229910052759 nickel Inorganic materials 0.000 claims description 13
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 10
- 229910052796 boron Inorganic materials 0.000 claims description 10
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 7
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 claims description 6
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical group [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims description 5
- 239000012467 final product Substances 0.000 claims description 5
- 239000005639 Lauric acid Substances 0.000 claims description 3
- 230000000694 effects Effects 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 239000002923 metal particle Substances 0.000 abstract description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 11
- 239000007787 solid Substances 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 229910002804 graphite Inorganic materials 0.000 description 8
- 239000010439 graphite Substances 0.000 description 8
- 238000003825 pressing Methods 0.000 description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 238000000280 densification Methods 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 4
- 239000000956 alloy Substances 0.000 description 4
- 229910045601 alloy Inorganic materials 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229910052750 molybdenum Inorganic materials 0.000 description 4
- 239000011733 molybdenum Substances 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000007596 consolidation process Methods 0.000 description 3
- NPURPEXKKDAKIH-UHFFFAOYSA-N iodoimino(oxo)methane Chemical compound IN=C=O NPURPEXKKDAKIH-UHFFFAOYSA-N 0.000 description 3
- 239000010687 lubricating oil Substances 0.000 description 3
- 239000013528 metallic particle Substances 0.000 description 3
- 239000007790 solid phase Substances 0.000 description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 238000005275 alloying Methods 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 238000010420 art technique Methods 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000005242 forging Methods 0.000 description 2
- 239000008240 homogeneous mixture Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 230000001131 transforming effect Effects 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000001513 hot isostatic pressing Methods 0.000 description 1
- 238000012886 linear function Methods 0.000 description 1
- HGPXWXLYXNVULB-UHFFFAOYSA-M lithium stearate Chemical compound [Li+].CCCCCCCCCCCCCCCCCC([O-])=O HGPXWXLYXNVULB-UHFFFAOYSA-M 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 238000010587 phase diagram Methods 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- 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
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/10—Sintering only
- B22F3/1035—Liquid phase sintering
-
- 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
- B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
- B22F1/10—Metallic powder containing lubricating or binding agents; Metallic powder containing organic material
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/02—Making ferrous alloys by powder metallurgy
- C22C33/0207—Using a mixture of prealloyed powders or a master alloy
-
- 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
- B22F2998/00—Supplementary information concerning processes or compositions relating to powder metallurgy
- B22F2998/10—Processes characterised by the sequence of their steps
Definitions
- This invention relates to a process for the compaction and sintering of powder metal. More particularly, this invention relates to a process for the compaction and sintering of powder metal employing complex transient liquid phase sintering.
- the prevalent method for producing low alloy steel powder metal parts involves the blending of either iron powder, co-diffused or low alloy steel powders or combinations thereof so that the sintered part contains such elements as nickel, chromium, molybdenum, copper, graphite and/or other alloying elements.
- Such powders are blended with lubricants to form a homogeneous mixture.
- the most commonly used lubricants are EBS (Ethylene Biostearamide), lithium stearate and zinc stearate. Such lubricants remain in solid form during the pressing operation.
- One known technique of producing a powder metal part involves the steps of mixing a powder metal mass with graphite and a lubricant, such as a PS1000 b lubricant supplied by APEX Advanced Materials, LLC, of Cleveland, Ohio, to form a generally homogeneous mixture and of thereafter pressing and sintering the mixture into a sintered product using a single press and sinter process.
- a lubricant such as a PS1000 b lubricant supplied by APEX Advanced Materials, LLC, of Cleveland, Ohio
- the invention provides a process in which a metal powder is mixed with a lubricant and at least one liquid phase former to form a mixture, compressed and then sintered into a dense product with a density of 99+% of theoretical.
- the lubricant that is used has a characteristic of transforming from a solid to a viscous liquid at low pressure and temperature and functions, in accordance with the invention, to distribute the liquid phase former over the particles of the metal powder.
- a lubricant is the above APEX PS1000 b lubricant that transforms from a solid to a viscous liquid when pressed in a compact at about 4 TSI at room temperature.
- Other suitable lubricants of this nature are lauric acid and Johnson's Floor Wax of the S.C. Johnson Company,
- the liquid phase former that is used has a characteristic of forming a liquid phase during sintering and of becoming part of the final product after sintering.
- the liquid phase former is at least one of synthetic graphite, nickel, boron, phosphorous and compounds of boron and phosphorous.
- Other liquid phase formers are aluminum, copper, molybdenum, nickel, silicon, sulfur, zinc and their alloys.
- the liquid phase former such as nickel, boron and phosphorous and compounds thereof should be finer than 20 microns and, preferably, finer than 10 microns whereas the synthetic graphite is finer than 10 microns and, preferably, finer than 2 microns.
- Compressing of the mixture is accomplished by means of uniaxial, cold isostatic or other consolidation methods at a pressure sufficient to liquefy and uniformly distribute the lubricant within the compressed mixture with the lubricant effecting a uniform distribution of the liquid phase former on the particles of the metal powder.
- the liquefied lubricant forms a liquid film between the mixture and the tool in which the mixture is being compacted to eliminate friction forces between the mixture and the tool so that a green compact with a uniform density throughout the compact is obtained.
- Sintering of the compressed mixture occurs at a sintering temperature sufficient to evaporate and drive off the lubricant and to effect a liquid phase sintering of the liquid phase former with the particles of the metal powder to obtain a compressed and sintered product having a density of 99+% of theoretical density.
- a sintering temperature sufficient to evaporate and drive off the lubricant and to effect a liquid phase sintering of the liquid phase former with the particles of the metal powder to obtain a compressed and sintered product having a density of 99+% of theoretical density.
- the process is particularly economic in obtaining ferrous or non-ferrous parts through a single pressing and sintering by coating the particles with a material that has a liquid phase forming component and that has high solubility of the solid phases.
- the invention provides a method of producing ferrous or non-ferrous powder metal parts which can be single pressed by conventional uniaxial (movement of a pressing tool in a single direction) or cold isostatic methods and sintered to full density without the need for further compaction or densification steps.
- a metal powder of elemental minus 100 ( ⁇ 100) mesh iron or low alloy steel is mixed with a lubricant that has a characteristic of transforming from a solid to a liquid under low pressure and temperature, e.g. 4TSI at room temperature, and of evaporating under a sintering temperature, for example APEX PS 1000 b, lauric Acid or Johnson's Floor Wax of S.C. Johnson Company, and a liquid phase former, such as extra fine synthetic graphite grade Timcal KS6, made by Timcal Ltd., of Bodio, Switzerland or less than 10 micron size graphite made by Asbury Carbon, Inc. of Asbury, N.J. that has a characteristic of forming a liquid phase during sintering and of becoming part of the final product after sintering.
- a lubricant that has a characteristic of transforming from a solid to a liquid under low pressure and temperature, e.g. 4TSI at room temperature, and of evaporating under a sintering
- the resultant mixture is then compacted at a pressure of in the range of from 30 to 70 tons per square inch or through use of high velocity compaction in a uniaxial or high compaction press and sintered at an appropriate temperature in the range of from 2070 to 2500 degrees F., in hydrogen and hydrogen based atmospheres, or nitrogen in an all graphite furnace or vacuum with a preferred temperature of from 2300 to 2500 degrees F. from 10 to 60 minutes at temperature to permit the metallic particles to densify to 99+% of theoretical density in the final product.
- the first required step is to distribute the liquid phase former uniformly around the solid phase particle, i.e. a metal powder particle, and to cause the liquid phase former to coat and bond to the metal powder particle with a high degree of uniformity on the majority of the powder metal particles.
- the surface and surface composition of the metal particle and the liquid phase former form a surface composition that upon further heating will liquefy forming a liquid film and provides surface tension which aids the densification process.
- the powder mixture of solid particle(s) of pure metal(s) or alloy(s) or co-diffused materials is blended with a lubricant (formulation) and one or more liquid phase former(s).
- the liquid phase formers generally become part of the final composition after sintering.
- the lubricant liquefies under pressure and is generally removed thermally in the sintering process.
- This powder blend (mixture) is compacted into a shape by means of uniaxial, cold isostatic or other consolidation methods where the pressure applied causes the lubricant to liquefy and be uniformly distributed.
- the liquid phase forms over the surface of the solid phase particles.
- the liquid lubricant is not the liquid phase former.
- the liquid phase formers are other components which either separately or in combination with the metallic particle surface forms a liquid phase during sintering.
- This process of distributing the liquid phase former is infinitely more effective than having a heterogeneous distribution that does not produce the potential amount of sites to cause an effective coverage and composition for liquid phase development.
- liquid lubricant such as APEX PS1000 b, which liquefy during compaction and are considered highly pressure sensitive that during compaction, the liquid lubricant disperses the fine liquid phase former uniformly over the surface of the particles whether the liquid phase former be synthetic graphite, boron, phosphorous or other liquid phase formers such as aluminum, copper, molybdenum, nickel, silicon, sulfur, zinc and their alloys.
- Typical manufacturing practice entails use of the prevalent method cited above in which Ancorsteel 85HP was blended with Southeastern Graphite grade 1651 in the amount of 0.65% although a range of 0.5-1.2% would be appropriate. Elemental nickel grade TD123 manufactured by Inco in an amount of 6.6% as well as a standard EBS lubricant in an amount of 1% were blended with the Ancorsteel 85HP and Southeastern Graphite grade 1651 to obtain a homogenous blend. This powder mixture was subsequently uniaxially compacted in both mechanical and hydraulic presses at 50 tons per square inch obtaining a green density of 7.05 g/cc. The resulting green compacts were then sintered at 2050 degrees F. in a nitrogen/hydrogen atmosphere for 45 minutes at temperature and obtained a sintered density of 7.15 g/cc to 7.20 g/cc (or 91.2% to 91.8% of theoretical density.)
- Ancorsteel 85HP was blended with Southeastern Graphite grade 1651 in the amount of 0.65% although a range of 0.5-1.2% would be appropriate. 6.6% of elemental nickel grade TD123 manufactured by Inco and EBS in an amount of 1% were blended with the Ancorsteel 85HP and Southeastern Graphite grade 1651 to obtain a homogenous blend. This powder mixture was subsequently uniaxially compacted in both mechanical and hydraulic presses at 50 tons per square inch obtaining a green density of 7.05 g/cc.
- the resulting green compacts were sintered in a nitrogen/hydrogen atmosphere at a higher temperature for 2440 F for 45 minutes at temperature and obtained a sintered density of 7.37 g/cc to 7.42 g/cc (or 94.0% to 94.6% of theoretical density.)
- iron powder, co-diffused or low alloy steel powders or combinations thereof were compacted so that the sintered part contained such elements as nickel, chromium, molybdenum, copper, low ash fine synthetic graphite and/or other alloying elements.
- the green compacts were sintered to a density of 7.84 g/cc or 100% of theoretical density.
- a powder metal namely, Ancorsteel 85HP
- APEX 1000b as the lubricant
- Elemental nickel grade TD123 manufactured by Inco was blended in the amount of 6.6% of with the Ancorsteel 85HP and APEX grade 1000b to obtain a homogenous blend.
- Extra fine synthetic graphite grade Timcal KS6 at a 0.65% addition with a particle size distribution of d50 3.3 um and d90 of 6.5 um was added (as the liquid phase former).
- This powder mixture was subsequently uniaxially compacted in both mechanical and hydraulic presses at 50 tons per square inch obtaining a green density of 7.15 g/cc.
- the resulting green compacts were sintered simultaneously with the above cited composition at 2440 degrees F. in a nitrogen/hydrogen atmosphere for 45 minutes at temperature to achieve a complex transient liquid phase sintering and obtained a sintered density of 7.84% (or 100% of theoretical density).
- Timcal KS4 and F10 were also found to be suitable for the process.
- the following table indicates the particle sizes that were suitable: Synthetic Graphite typical particle size maximum particle size (Timcal) (microns) (microns) F10 5.8 12.0 KS6 3.3 6.5 KS4 2.4 4.7
- Synthetic Graphite typical particle size (Asbury) (microns) 4827 2.0 4794 5.0 PM5 & PFSS 4.0 t 7.0 PI5 3.75 to 6.25 PFS8 6.0 to 11.0
- the nickel that was used was obtained from INCO Special Products, INCO Limited of Wyckoff, N.J. and the following were found suitable: Fine Nickel Powder average particle size (INCO) (microns) 123 1 to 2 255 2.2 to 2.8 287 2.6 to 3.3 110 0.8 to 1.5 210 0.5 to 1.0 210H 0.2 to 0.5
- ICO Fine Nickel Powder average particle size
- the invention thus provides a method of creating a powder metal master alloy or blend of metal powder with liquid phase formers which permit such powders to be pressed and sintered to close to full density.
- the invention provides the ability to produce a highly uniform green density compact with no density split because the liquid lubricant eliminates density splits.
- Density splits are caused when die wall friction exists and as a result, when pressing from top to bottom, the densities facing the top and bottom punches are higher than in the center of the compact. In effect, an “hour glass” density profile occurs in the final product.
- Elimination of density splits allows high precision and avoidable distortion when sintering to full density because non-uniform shrinkage of the part due to density variation is eliminated.
- the lubricant liquefies upon compaction thereby coating the tooling in which the blended mass of material is being compacted thus giving a liquid film between the tool and the developing compact.
- This liquid between the tool and compact drives the friction force to zero thus eliminating density gradients within the compact.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Powder Metallurgy (AREA)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/724,248 US20050118053A1 (en) | 2003-11-28 | 2003-11-28 | Process for complex transient liquid phase sintering of powder metal |
| PCT/US2004/039720 WO2005053882A2 (fr) | 2003-11-28 | 2004-11-22 | Procede de frittage en phase liquide transitoire complexe de poudre metallique |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/724,248 US20050118053A1 (en) | 2003-11-28 | 2003-11-28 | Process for complex transient liquid phase sintering of powder metal |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20050118053A1 true US20050118053A1 (en) | 2005-06-02 |
Family
ID=34620042
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/724,248 Abandoned US20050118053A1 (en) | 2003-11-28 | 2003-11-28 | Process for complex transient liquid phase sintering of powder metal |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US20050118053A1 (fr) |
| WO (1) | WO2005053882A2 (fr) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070048166A1 (en) * | 2005-08-26 | 2007-03-01 | Apex Advanced Technologies, Llc | Powder metal composition containing micronized deformable solids and methods of making and using the same |
| US20070077164A1 (en) * | 2005-10-03 | 2007-04-05 | Apex Advanced Technologies, Llc | Powder metallurgy methods and compositions |
| CN105033259A (zh) * | 2015-06-25 | 2015-11-11 | 马鞍山市华东粉末冶金厂 | 一种粉末冶金制备汽车座椅升降器轴承套的方法及产品 |
| US20160327144A1 (en) * | 2014-01-22 | 2016-11-10 | Ntn Corporation | Sintered machine part and manufacturing method thereof |
Citations (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3785801A (en) * | 1968-03-01 | 1974-01-15 | Int Nickel Co | Consolidated composite materials by powder metallurgy |
| US3841870A (en) * | 1973-03-07 | 1974-10-15 | Carpenter Technology Corp | Method of making articles from powdered material requiring forming at high temperature |
| US3900936A (en) * | 1972-10-31 | 1975-08-26 | Parker Pen Co | Cemented ferrochrome material |
| US4002474A (en) * | 1975-07-31 | 1977-01-11 | H. L. Blachford Limited | Lubricants for powdered metals |
| US4098608A (en) * | 1975-11-12 | 1978-07-04 | B.S.A. Sintered Components Limited | Metal powder compositions |
| US4106932A (en) * | 1974-07-31 | 1978-08-15 | H. L. Blachford Limited | Lubricants for powdered metals, and powdered metal compositions containing said lubricants |
| US4618473A (en) * | 1985-06-14 | 1986-10-21 | General Motors Corporation | Iron powder article having improved toughness |
| US5538684A (en) * | 1994-08-12 | 1996-07-23 | Hoeganaes Corporation | Powder metallurgy lubricant composition and methods for using same |
| US5744433A (en) * | 1994-06-02 | 1998-04-28 | Hoganas Ab | Metal powder composition for warm compaction and method for producing sintered products |
| US6235076B1 (en) * | 1997-03-19 | 2001-05-22 | Kawasaki Steel Corporation | Iron base powder mixture for powder metallurgy excellent in fluidity and moldability, method of production thereof, and method of production of molded article by using the iron base powder mixture |
| US20020159910A1 (en) * | 2000-04-28 | 2002-10-31 | Christer Aslund | Method for sintering a carbon steel part using a hydrocolloid binder as carbon source |
| US6537489B2 (en) * | 2000-11-09 | 2003-03-25 | Höganäs Ab | High density products and method for the preparation thereof |
| US6767505B2 (en) * | 2000-07-12 | 2004-07-27 | Utron Inc. | Dynamic consolidation of powders using a pulsed energy source |
| US6887295B2 (en) * | 2002-10-25 | 2005-05-03 | Hoeganaes Corporation | Powder metallurgy lubricants, compositions, and methods for using the same |
-
2003
- 2003-11-28 US US10/724,248 patent/US20050118053A1/en not_active Abandoned
-
2004
- 2004-11-22 WO PCT/US2004/039720 patent/WO2005053882A2/fr not_active Ceased
Patent Citations (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3785801A (en) * | 1968-03-01 | 1974-01-15 | Int Nickel Co | Consolidated composite materials by powder metallurgy |
| US3900936A (en) * | 1972-10-31 | 1975-08-26 | Parker Pen Co | Cemented ferrochrome material |
| US3841870A (en) * | 1973-03-07 | 1974-10-15 | Carpenter Technology Corp | Method of making articles from powdered material requiring forming at high temperature |
| US4106932A (en) * | 1974-07-31 | 1978-08-15 | H. L. Blachford Limited | Lubricants for powdered metals, and powdered metal compositions containing said lubricants |
| US4002474A (en) * | 1975-07-31 | 1977-01-11 | H. L. Blachford Limited | Lubricants for powdered metals |
| US4098608A (en) * | 1975-11-12 | 1978-07-04 | B.S.A. Sintered Components Limited | Metal powder compositions |
| US4618473A (en) * | 1985-06-14 | 1986-10-21 | General Motors Corporation | Iron powder article having improved toughness |
| US5744433A (en) * | 1994-06-02 | 1998-04-28 | Hoganas Ab | Metal powder composition for warm compaction and method for producing sintered products |
| US5538684A (en) * | 1994-08-12 | 1996-07-23 | Hoeganaes Corporation | Powder metallurgy lubricant composition and methods for using same |
| US6235076B1 (en) * | 1997-03-19 | 2001-05-22 | Kawasaki Steel Corporation | Iron base powder mixture for powder metallurgy excellent in fluidity and moldability, method of production thereof, and method of production of molded article by using the iron base powder mixture |
| US20020159910A1 (en) * | 2000-04-28 | 2002-10-31 | Christer Aslund | Method for sintering a carbon steel part using a hydrocolloid binder as carbon source |
| US6767505B2 (en) * | 2000-07-12 | 2004-07-27 | Utron Inc. | Dynamic consolidation of powders using a pulsed energy source |
| US6537489B2 (en) * | 2000-11-09 | 2003-03-25 | Höganäs Ab | High density products and method for the preparation thereof |
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| US20070048166A1 (en) * | 2005-08-26 | 2007-03-01 | Apex Advanced Technologies, Llc | Powder metal composition containing micronized deformable solids and methods of making and using the same |
| US7892314B2 (en) * | 2005-08-26 | 2011-02-22 | Apex Advanced Technologies, Llc | Powder metal composition containing micronized deformable solids and methods of making and using the same |
| US20070077164A1 (en) * | 2005-10-03 | 2007-04-05 | Apex Advanced Technologies, Llc | Powder metallurgy methods and compositions |
| WO2007041399A2 (fr) | 2005-10-03 | 2007-04-12 | Apex Advanced Technologies, Llc | Procedes et compositions de metallurgie des poudres |
| US20090162236A1 (en) * | 2005-10-03 | 2009-06-25 | Apex Advanced Technologies, Llc | Powder Metallurgy Methods And Compositions |
| EP1931808A4 (fr) * | 2005-10-03 | 2010-06-16 | Apex Advanced Technologies Llc | Procedes et compositions de metallurgie des poudres |
| US8062582B2 (en) * | 2005-10-03 | 2011-11-22 | Apex Advanced Technologies, Llc | Powder metallurgy methods and compositions |
| US20160327144A1 (en) * | 2014-01-22 | 2016-11-10 | Ntn Corporation | Sintered machine part and manufacturing method thereof |
| CN105033259A (zh) * | 2015-06-25 | 2015-11-11 | 马鞍山市华东粉末冶金厂 | 一种粉末冶金制备汽车座椅升降器轴承套的方法及产品 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2005053882A2 (fr) | 2005-06-16 |
| WO2005053882A3 (fr) | 2005-11-03 |
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