US20110002805A1 - Formable sintered alloy with dispersed hard phase - Google Patents
Formable sintered alloy with dispersed hard phase Download PDFInfo
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- US20110002805A1 US20110002805A1 US12/837,720 US83772010A US2011002805A1 US 20110002805 A1 US20110002805 A1 US 20110002805A1 US 83772010 A US83772010 A US 83772010A US 2011002805 A1 US2011002805 A1 US 2011002805A1
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- 229910045601 alloy Inorganic materials 0.000 title description 3
- 239000000956 alloy Substances 0.000 title description 3
- 238000000034 method Methods 0.000 claims abstract description 25
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 20
- 229910000734 martensite Inorganic materials 0.000 claims abstract description 8
- 238000001816 cooling Methods 0.000 claims abstract description 7
- 239000011159 matrix material Substances 0.000 claims abstract description 7
- 229910001562 pearlite Inorganic materials 0.000 claims abstract description 7
- 229910052742 iron Inorganic materials 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims description 32
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
- 239000012535 impurity Substances 0.000 claims description 8
- 239000000314 lubricant Substances 0.000 claims description 6
- 238000005245 sintering Methods 0.000 claims description 6
- 230000000087 stabilizing effect Effects 0.000 claims description 6
- 238000005056 compaction Methods 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 238000005496 tempering Methods 0.000 claims description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 238000010791 quenching Methods 0.000 description 3
- 230000000171 quenching effect Effects 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 2
- 238000005275 alloying Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- 0 *C=C(CC1)*=C1*=C1CC1 Chemical compound *C=C(CC1)*=C1*=C1CC1 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000012255 powdered metal Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/22—Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
-
- 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
- C22C33/0257—Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements
- C22C33/0278—Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements with at least one alloying element having a minimum content above 5%
- C22C33/0285—Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements with at least one alloying element having a minimum content above 5% with Cr, Co, or Ni having a minimum content higher than 5%
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/20—Ferrous alloys, e.g. steel alloys containing chromium with copper
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/42—Ferrous alloys, e.g. steel alloys containing chromium with nickel with copper
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/44—Ferrous alloys, e.g. steel alloys containing chromium with nickel with molybdenum or tungsten
Definitions
- This invention relates to a formable sintered alloy with dispersed hard phase.
- At least one advantage of the present invention is provided by a method of forming an iron based sintered body having a microstructure of about 20-50% dispersed martensite in a matrix of fine pearlite, the method comprising the steps of: providing a mixture comprising a composition in % by mass: 0.4 to 1.0% of C; 0.5 to 3.5% of Cr; 0.1 to 1.7% of Mo; 0.3 to 3.0% of Cu, the balance being primarily Fe and unavoidable impurities and lubricant; placing the mixture in a first mold possessing the approximate shape of a finished product; subjecting the mold to compaction pressures of between generally 35 and 65 tsi to produce a green body compact; sintering the green body compact at a temperature of between 1120 ⁇ C and 1180 ⁇ C to form a sintered article; cooling the sintered article at a rate not exceeding 0.5 ⁇ C/sec; thermally stabilizing the sintered article; placing the sintered article in a second mold possessing the desired shape of the finished product; and subject
- At least one advantage of the present invention is provided by a A method of forming an iron based sintered body having a microstructure of about 20-50% dispersed martensite in a matrix of fine pearlite, the method comprising the steps of: providing a mixture comprising a composition in % by mass: 0.4 to 1.0% of C; 0.5 to 3.5% of Cr; 0.1 to 1.7% of Mo; 0.3 to 3.0% of Cu, the balance being primarily Fe and unavoidable impurities and lubricant; placing the mixture in a first mold possessing the approximate shape of a finished product; subjecting the mold to compaction pressures of between generally 35 and 65 tsi to produce a green body compact; sintering the green body compact at a temperature of between 1120 ⁇ C and 1180 ⁇ C in an atmosphere comprising about 90% nitrogen and 10% hydrogen for about 25 minutes to form a sintered article; cooling the sintered article at a rate not exceeding 0.5 ⁇ C/sec; thermally stabilizing the sintered article; placing the sintered article in
- FIG. 1 is a microscopic view of an embodiment of the iron based sintered material of the present invention
- FIG. 2 is a wear plot of a prior art gear after an accelerated pump durability wear test
- FIG. 3 is a perspective view of a portion of the prior art gear of FIG. 2 showing wear on the gear surface;
- FIG. 4 is a wear plot of a embodiment of a gear of the present invention after the same accelerated pump durability wear test that the prior art gear of FIGS. 2-3 were subjected to;
- FIG. 5 is a perspective view of a portion of the gear of FIG. 4 showing light burnishing on the gear surface.
- FIG. 1 A microscopic view of an embodiment of the composition of the present invention is shown in FIG. 1 .
- the lean composition achieves desired microstructure/properties and associated sliding wear resistance with reduced content of expensive alloying ingredients.
- the constituent ingredients demonstrate sufficient hardenability to achieve martensitic transformation at cooling rates attainable in conventional furnaces thereby leveraging existing installed capacity and deferring capital investment in specialized furnaces.
- the constituent ingredients demonstrate sufficient hardenability to achieve martensitic transformation at cooling rates attainable in conventional furnaces thereby avoiding the dimensional distortion penalty associated with rapid quenching by oil baths and/or gas pressure quenching.
- the volume fraction of fine pearlite matrix of generally 70% affords sufficient formability to achieve a high degree of dimensional accuracy required of net-shape sintered articles. Forming may be performed without supplemental part heating, tool heating, intermediate quenching and thereby avoids the associated operational complexity and cost of warm/hot forming processes.
- An embodiment of the iron-base alloy of the present invention comprises a 20 to 50% weight fraction of prealloy steel of composition A and a 48 to 78% weight fraction of prealloy steel of composition B to which additional alloying elements (and lubricant) are added in preparation of a powdered metal blended mixture.
- the resulting mixture composition of the embodiment comprises in % by mass: 0.4 to 1.0% of C; 0.5 to 3.5% of Cr; 0.1 to 1.7% of Mo; 0.3 to 3.0% of Cu; and the balance being primarily Fe and unavoidable impurities. (The lubricant will volatilize during sinter and as such is not reflected in the composition %).
- the mixture is placed in a mold possessing the approximate shape of the finished product and subjected to compaction pressures of between generally 35 and 65 tsi to produce a green body compact.
- the green body compact is subsequently sintered at a temperature of between 1120 ⁇ C and 1180 ⁇ C for about 25 minutes in an atmosphere comprised of 90% nitrogen and 10% hydrogen.
- the sintered article subsequently is cooled at a rate not exceeding 0.5 ⁇ C/sec producing a sinter-hardened composite wear resistant microstructure of approximately 20 to 50% dispersed martensite in a matrix of fine pearlite.
- the sintered article subsequently is subjected to cold treatment and tempering for thermal stabilization.
- the sintered article Upon completion of thermal treatment, the sintered article is placed in a mold possessing the desired shape of the finished product and subsequently subjected to forming pressures generally between 50 and 75 tsi to achieve dimensional refinement enabling production of discretely toleranced net-shape features.
- the sintered and formed article demonstrates acceptable sliding wear properties for pumping elements employed with ultra low sulfur diesel fuels (Shell MJ04 U.S. Worst Case Diesel) while offering the costs advantages of lean composition and reduced process complexity in comparison to prior art.
- Nickel may be added such that the resulting mixture composition of the embodiment comprises in % by mass: 0.4 to 1.0% of C; 0.5 to 3.5% of Cr; 0.1 to 1.7% of Mo; 0.3 to 3.0% of Cu; 0.1 to 6.0% Ni; and the balance being primarily Fe and unavoidable impurities.
- the resulting mixture composition of the embodiment comprises in % by mass: 0.4 to 1.0% of C; 0.5 to 3.5% of Cr; 0.1 to 1.7% of Mo; 0.3 to 3.0% of Cu; 0.1 to 0.5% Mn; and the balance being primarily Fe and unavoidable impurities.
- the resulting mixture composition of the embodiment comprises in % by mass: 0.4 to 1.0% of C; 0.5 to 3.5% of Cr; 0.1 to 1.7% of Mo; 0.3 to 3.0% of Cu; 0.1 to 6.0% Ni; 0.1 to 0.5% Mn; and the balance being primarily Fe and unavoidable impurities.
- the sintered and formed article may be a gear, such as a gear for a gerotor.
- Testing of a sintered and formed gear in accordance with the present invention was subjected to an accelerated pump durability test with the results of the prior art control gear shown in FIGS. 2 and 3 and the results of the gear of the present invention shown in FIGS. 4 and 5 .
- FIGS. 2 and 4 are wear plots showing the magnitude of the surface wear of the gear teeth by vector representation. While the wear in FIG. 2 is significantly more than the gear of the present invention shown in FIG. 4 , it is noted that the wear shown in FIG. 4 is magnified at a scale twice that of FIG. 2 in order to see the wear. It is also noted that non-wear portions of the wear plot of FIG. 4 caused by offset have been removed from the original plot to eliminate any confusion from the wear comparison.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Powder Metallurgy (AREA)
Abstract
A method of forming an iron based sintered body which comprises in % by mass: 0.4 to 1.0% of C; 0.5 to 3.5% of Cr; 0.1 to 1.7% of Mo; 0.3 to 3.0% of Cu and microstructure of about 20-50% dispersed martensite in a matrix of fine pearlite is provided. The method utilizes a step of cooling a sintered article at a rate not exceeding 0.5˜C/sec. Ni and/or Mn may also be included in the method.
Description
- This application is a continuation of U.S. Non-Provisional application Ser. No. 12/339,565 filed Dec. 19, 2008, which claims the benefit of U.S. Provisional Application No. 61/015,024 filed Dec. 19, 2007, both of which are hereby incorporated by reference.
- This invention relates to a formable sintered alloy with dispersed hard phase.
- At least one advantage of the present invention is provided by a method of forming an iron based sintered body having a microstructure of about 20-50% dispersed martensite in a matrix of fine pearlite, the method comprising the steps of: providing a mixture comprising a composition in % by mass: 0.4 to 1.0% of C; 0.5 to 3.5% of Cr; 0.1 to 1.7% of Mo; 0.3 to 3.0% of Cu, the balance being primarily Fe and unavoidable impurities and lubricant; placing the mixture in a first mold possessing the approximate shape of a finished product; subjecting the mold to compaction pressures of between generally 35 and 65 tsi to produce a green body compact; sintering the green body compact at a temperature of between 1120˜C and 1180˜C to form a sintered article; cooling the sintered article at a rate not exceeding 0.5˜C/sec; thermally stabilizing the sintered article; placing the sintered article in a second mold possessing the desired shape of the finished product; and subjecting the second mold to pressures generally between 50 and 75 tsi.
- At least one advantage of the present invention is provided by a A method of forming an iron based sintered body having a microstructure of about 20-50% dispersed martensite in a matrix of fine pearlite, the method comprising the steps of: providing a mixture comprising a composition in % by mass: 0.4 to 1.0% of C; 0.5 to 3.5% of Cr; 0.1 to 1.7% of Mo; 0.3 to 3.0% of Cu, the balance being primarily Fe and unavoidable impurities and lubricant; placing the mixture in a first mold possessing the approximate shape of a finished product; subjecting the mold to compaction pressures of between generally 35 and 65 tsi to produce a green body compact; sintering the green body compact at a temperature of between 1120˜C and 1180˜C in an atmosphere comprising about 90% nitrogen and 10% hydrogen for about 25 minutes to form a sintered article; cooling the sintered article at a rate not exceeding 0.5˜C/sec; thermally stabilizing the sintered article; placing the sintered article in a second mold possessing the desired shape of the finished product; and subjecting the second mold to pressures generally between 50 and 75 tsi.
- Embodiments of this invention will now be described in further detail with reference to the accompanying drawing, in which:
-
FIG. 1 is a microscopic view of an embodiment of the iron based sintered material of the present invention; -
FIG. 2 is a wear plot of a prior art gear after an accelerated pump durability wear test; -
FIG. 3 is a perspective view of a portion of the prior art gear ofFIG. 2 showing wear on the gear surface; -
FIG. 4 is a wear plot of a embodiment of a gear of the present invention after the same accelerated pump durability wear test that the prior art gear ofFIGS. 2-3 were subjected to; and -
FIG. 5 is a perspective view of a portion of the gear ofFIG. 4 showing light burnishing on the gear surface. - A microscopic view of an embodiment of the composition of the present invention is shown in
FIG. 1 . The lean composition achieves desired microstructure/properties and associated sliding wear resistance with reduced content of expensive alloying ingredients. The constituent ingredients demonstrate sufficient hardenability to achieve martensitic transformation at cooling rates attainable in conventional furnaces thereby leveraging existing installed capacity and deferring capital investment in specialized furnaces. The constituent ingredients demonstrate sufficient hardenability to achieve martensitic transformation at cooling rates attainable in conventional furnaces thereby avoiding the dimensional distortion penalty associated with rapid quenching by oil baths and/or gas pressure quenching. The volume fraction of fine pearlite matrix of generally 70% affords sufficient formability to achieve a high degree of dimensional accuracy required of net-shape sintered articles. Forming may be performed without supplemental part heating, tool heating, intermediate quenching and thereby avoids the associated operational complexity and cost of warm/hot forming processes. - An embodiment of the iron-base alloy of the present invention comprises a 20 to 50% weight fraction of prealloy steel of composition A and a 48 to 78% weight fraction of prealloy steel of composition B to which additional alloying elements (and lubricant) are added in preparation of a powdered metal blended mixture. The resulting mixture composition of the embodiment comprises in % by mass: 0.4 to 1.0% of C; 0.5 to 3.5% of Cr; 0.1 to 1.7% of Mo; 0.3 to 3.0% of Cu; and the balance being primarily Fe and unavoidable impurities. (The lubricant will volatilize during sinter and as such is not reflected in the composition %). The mixture is placed in a mold possessing the approximate shape of the finished product and subjected to compaction pressures of between generally 35 and 65 tsi to produce a green body compact. The green body compact is subsequently sintered at a temperature of between 1120˜C and 1180˜C for about 25 minutes in an atmosphere comprised of 90% nitrogen and 10% hydrogen. The sintered article subsequently is cooled at a rate not exceeding 0.5˜C/sec producing a sinter-hardened composite wear resistant microstructure of approximately 20 to 50% dispersed martensite in a matrix of fine pearlite. The sintered article subsequently is subjected to cold treatment and tempering for thermal stabilization. Upon completion of thermal treatment, the sintered article is placed in a mold possessing the desired shape of the finished product and subsequently subjected to forming pressures generally between 50 and 75 tsi to achieve dimensional refinement enabling production of discretely toleranced net-shape features. The sintered and formed article demonstrates acceptable sliding wear properties for pumping elements employed with ultra low sulfur diesel fuels (Shell MJ04 U.S. Worst Case Diesel) while offering the costs advantages of lean composition and reduced process complexity in comparison to prior art.
- In one embodiment, Nickel may be added such that the resulting mixture composition of the embodiment comprises in % by mass: 0.4 to 1.0% of C; 0.5 to 3.5% of Cr; 0.1 to 1.7% of Mo; 0.3 to 3.0% of Cu; 0.1 to 6.0% Ni; and the balance being primarily Fe and unavoidable impurities. In another embodiment, the resulting mixture composition of the embodiment comprises in % by mass: 0.4 to 1.0% of C; 0.5 to 3.5% of Cr; 0.1 to 1.7% of Mo; 0.3 to 3.0% of Cu; 0.1 to 0.5% Mn; and the balance being primarily Fe and unavoidable impurities. In still another embodiment, the resulting mixture composition of the embodiment comprises in % by mass: 0.4 to 1.0% of C; 0.5 to 3.5% of Cr; 0.1 to 1.7% of Mo; 0.3 to 3.0% of Cu; 0.1 to 6.0% Ni; 0.1 to 0.5% Mn; and the balance being primarily Fe and unavoidable impurities.
- In one embodiment, the sintered and formed article may be a gear, such as a gear for a gerotor. Testing of a sintered and formed gear in accordance with the present invention was subjected to an accelerated pump durability test with the results of the prior art control gear shown in
FIGS. 2 and 3 and the results of the gear of the present invention shown inFIGS. 4 and 5 .FIGS. 2 and 4 are wear plots showing the magnitude of the surface wear of the gear teeth by vector representation. While the wear inFIG. 2 is significantly more than the gear of the present invention shown inFIG. 4 , it is noted that the wear shown inFIG. 4 is magnified at a scale twice that ofFIG. 2 in order to see the wear. It is also noted that non-wear portions of the wear plot ofFIG. 4 caused by offset have been removed from the original plot to eliminate any confusion from the wear comparison. - Although the principles, embodiments and operation of the present invention have been described in detail herein, this is not to be construed as being limited to the particular illustrative forms disclosed. They will thus become apparent to those skilled in the art that various modifications of the embodiments herein can be made without departing from the spirit or scope of the invention. Accordingly, the scope and content of the present invention are to be defined only by the terms of the appended claims.
Claims (14)
1. A method of forming an iron based sintered body having a microstructure of about 20-50% dispersed martensite in a matrix of fine pearlite, the method comprising the steps of:
providing a mixture comprising a composition in % by mass: 0.4 to 1.0% of C; 0.5 to 3.5% of Cr; 0.1 to 1.7% of Mo; 0.3 to 3.0% of Cu, the balance being primarily Fe and unavoidable impurities and lubricant;
placing the mixture in a first mold possessing the approximate shape of a finished product;
subjecting the mold to compaction pressures of between generally 35 and 65 tsi to produce a green body compact;
sintering the green body compact at a temperature of between 1120˜C and 1180˜C to form a sintered article;
cooling the sintered article at a rate not exceeding 0.5˜C/sec;
thermally stabilizing the sintered article;
placing the sintered article in a second mold possessing the desired shape of the finished product;
subjecting the second mold to pressures generally between 50 and 75 tsi.
2. The method of claim 1 wherein the step of sintering the green body compact is performed in an atmosphere comprising about 90% nitrogen and 10% hydrogen.
3. The method of claim 1 wherein the step of thermally stabilizing the sintered article comprises cold treatment and tempering.
4. The method of claim 1 , wherein the step of providing a mixture further includes in % by mass: 0.1 to 0.5 of Mn.
5. The method of claim 1 , wherein the step of providing a mixture further includes in % by mass: 0.1 to 6.0 of Ni.
6. The method of claim 1 , wherein the first mold is in the form of a gerotor gear.
7. The method of claim 1 , wherein the second mold is in the form of a gerotor gear generally at net shape.
8. The method of claim 1 , wherein the step of sintering the green body compact at a temperature of between 1120˜C and 1180˜C is performed for about 25 minutes.
9. A method of forming an iron based sintered body having a microstructure of about 20-50% dispersed martensite in a matrix of fine pearlite, the method comprising the steps of:
providing a mixture comprising a composition in % by mass: 0.4 to 1.0% of C; 0.5 to 3.5% of Cr; 0.1 to 1.7% of Mo; 0.3 to 3.0% of Cu, the balance being primarily Fe and unavoidable impurities and lubricant;
placing the mixture in a first mold possessing the approximate shape of a finished product;
subjecting the mold to compaction pressures of between generally 35 and 65 tsi to produce a green body compact;
sintering the green body compact at a temperature of between 1120˜C and 1180˜C in an atmosphere comprising about 90% nitrogen and 10% hydrogen for about 25 minutes to form a sintered article;
cooling the sintered article at a rate not exceeding 0.5˜C/sec;
thermally stabilizing the sintered article;
placing the sintered article in a second mold possessing the desired shape of the finished product;
subjecting the second mold to pressures generally between 50 and 75 tsi.
10. The method of claim 9 wherein the step of thermally stabilizing the sintered article comprises cold treatment and tempering.
11. The method of claim 9 , wherein the step of providing a mixture further includes in % by mass: 0.1 to 0.5 of Mn.
12. The method of claim 9 , wherein the step of providing a mixture further includes in % by mass: 0.1 to 6.0 of Ni.
13. The method of claim 9 , wherein the first mold is in the form of a gerotor gear.
14. The method of claim 9 , wherein the second mold is in the form of a gerotor gear generally at net shape.
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US12/837,720 US20110002805A1 (en) | 2007-12-19 | 2010-07-16 | Formable sintered alloy with dispersed hard phase |
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US1502407P | 2007-12-19 | 2007-12-19 | |
US12/339,565 US20090162241A1 (en) | 2007-12-19 | 2008-12-19 | Formable sintered alloy with dispersed hard phase |
US12/837,720 US20110002805A1 (en) | 2007-12-19 | 2010-07-16 | Formable sintered alloy with dispersed hard phase |
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US12/339,565 Continuation US20090162241A1 (en) | 2007-12-19 | 2008-12-19 | Formable sintered alloy with dispersed hard phase |
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US12/837,720 Abandoned US20110002805A1 (en) | 2007-12-19 | 2010-07-16 | Formable sintered alloy with dispersed hard phase |
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EP3296418A1 (en) * | 2016-09-16 | 2018-03-21 | Toyota Jidosha Kabushiki Kaisha | Manufacturing method of wear-resistant iron-based sintered alloy and wear-resistant iron-based sintered alloy |
CN110434344A (en) * | 2019-08-30 | 2019-11-12 | 广东光铭新材料科技有限公司 | A kind of motor gear and preparation method thereof |
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RU2618976C2 (en) | 2012-01-05 | 2017-05-11 | Хеганес Аб (Пабл) | New metal powder and its use |
CN103600062B (en) * | 2013-10-10 | 2016-01-13 | 铜陵新创流体科技有限公司 | A kind of sintered alloy composite and preparation method thereof |
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Cited By (2)
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EP3296418A1 (en) * | 2016-09-16 | 2018-03-21 | Toyota Jidosha Kabushiki Kaisha | Manufacturing method of wear-resistant iron-based sintered alloy and wear-resistant iron-based sintered alloy |
CN110434344A (en) * | 2019-08-30 | 2019-11-12 | 广东光铭新材料科技有限公司 | A kind of motor gear and preparation method thereof |
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