US20030103858A1 - Metallurgical powder compositions and methods of making and using the same - Google Patents
Metallurgical powder compositions and methods of making and using the same Download PDFInfo
- Publication number
- US20030103858A1 US20030103858A1 US10/266,316 US26631602A US2003103858A1 US 20030103858 A1 US20030103858 A1 US 20030103858A1 US 26631602 A US26631602 A US 26631602A US 2003103858 A1 US2003103858 A1 US 2003103858A1
- Authority
- US
- United States
- Prior art keywords
- weight percent
- iron
- powder
- metallurgical
- molybdenum
- 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
- 239000000843 powder Substances 0.000 title claims abstract description 260
- 239000000203 mixture Substances 0.000 title claims abstract description 136
- 238000000034 method Methods 0.000 title claims description 47
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 141
- 229910000640 Fe alloy Inorganic materials 0.000 claims abstract description 61
- 229910052742 iron Inorganic materials 0.000 claims abstract description 55
- 229910052751 metal Inorganic materials 0.000 claims abstract description 54
- 239000002184 metal Substances 0.000 claims abstract description 54
- 238000005275 alloying Methods 0.000 claims abstract description 53
- 239000000654 additive Substances 0.000 claims abstract description 44
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 41
- 230000000996 additive effect Effects 0.000 claims abstract description 26
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 8
- 239000010439 graphite Substances 0.000 claims abstract description 8
- 238000004519 manufacturing process Methods 0.000 claims abstract description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical group [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 35
- 229910052750 molybdenum Inorganic materials 0.000 claims description 35
- 239000011733 molybdenum Substances 0.000 claims description 35
- 239000010949 copper Substances 0.000 claims description 30
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 29
- 229910052802 copper Inorganic materials 0.000 claims description 28
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 22
- 229910052799 carbon Inorganic materials 0.000 claims description 20
- 229910052759 nickel Inorganic materials 0.000 claims description 11
- 239000011651 chromium Substances 0.000 claims description 10
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 9
- 229910052804 chromium Inorganic materials 0.000 claims description 8
- 238000005245 sintering Methods 0.000 claims description 7
- 229910052720 vanadium Inorganic materials 0.000 claims description 7
- 229910001182 Mo alloy Inorganic materials 0.000 claims description 6
- CADICXFYUNYKGD-UHFFFAOYSA-N sulfanylidenemanganese Chemical compound [Mn]=S CADICXFYUNYKGD-UHFFFAOYSA-N 0.000 claims description 6
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 6
- 229910052721 tungsten Inorganic materials 0.000 claims description 6
- 239000010937 tungsten Substances 0.000 claims description 6
- DSMZRNNAYQIMOM-UHFFFAOYSA-N iron molybdenum Chemical compound [Fe].[Fe].[Mo] DSMZRNNAYQIMOM-UHFFFAOYSA-N 0.000 claims 3
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims 1
- 239000011230 binding agent Substances 0.000 description 32
- 239000002245 particle Substances 0.000 description 25
- 239000000314 lubricant Substances 0.000 description 24
- KWUUWVQMAVOYKS-UHFFFAOYSA-N iron molybdenum Chemical compound [Fe].[Fe][Mo][Mo] KWUUWVQMAVOYKS-UHFFFAOYSA-N 0.000 description 16
- 229910000831 Steel Inorganic materials 0.000 description 10
- 238000003754 machining Methods 0.000 description 10
- 239000010959 steel Substances 0.000 description 10
- 229910045601 alloy Inorganic materials 0.000 description 9
- 239000000956 alloy Substances 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 8
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 8
- 239000010703 silicon Substances 0.000 description 8
- 239000012535 impurity Substances 0.000 description 7
- 229910052710 silicon Inorganic materials 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 6
- 238000009792 diffusion process Methods 0.000 description 6
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 description 6
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 6
- 239000001993 wax Substances 0.000 description 6
- 238000005056 compaction Methods 0.000 description 5
- 238000009826 distribution Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- 238000005553 drilling Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000010955 niobium Substances 0.000 description 4
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 4
- 239000011574 phosphorus Substances 0.000 description 4
- 239000004014 plasticizer Substances 0.000 description 4
- -1 polyethylene Polymers 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- 229910052748 manganese Inorganic materials 0.000 description 3
- 239000011572 manganese Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- RKISUIUJZGSLEV-UHFFFAOYSA-N n-[2-(octadecanoylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCNC(=O)CCCCCCCCCCCCCCCCC RKISUIUJZGSLEV-UHFFFAOYSA-N 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 229910052581 Si3N4 Inorganic materials 0.000 description 2
- 229910001128 Sn alloy Inorganic materials 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 238000000137 annealing Methods 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 229910002056 binary alloy Inorganic materials 0.000 description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical class [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 238000002356 laser light scattering Methods 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 150000001247 metal acetylides Chemical class 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229910052758 niobium Inorganic materials 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 238000004663 powder metallurgy Methods 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 238000005204 segregation Methods 0.000 description 2
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000004763 sulfides Chemical class 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 239000011135 tin Substances 0.000 description 2
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 229910000521 B alloy Inorganic materials 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 229910000599 Cr alloy Inorganic materials 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229910001021 Ferroalloy Inorganic materials 0.000 description 1
- 229910000604 Ferrochrome Inorganic materials 0.000 description 1
- 229910001309 Ferromolybdenum Inorganic materials 0.000 description 1
- MBMLMWLHJBBADN-UHFFFAOYSA-N Ferrous sulfide Chemical class [Fe]=S MBMLMWLHJBBADN-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 229910017970 MgO-SiO2 Inorganic materials 0.000 description 1
- 229910000914 Mn alloy Inorganic materials 0.000 description 1
- 229910001096 P alloy Inorganic materials 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229910000676 Si alloy Inorganic materials 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BLRUBJIXUVIYEA-UHFFFAOYSA-N [Mn].[Fe].[Mo] Chemical compound [Mn].[Fe].[Mo] BLRUBJIXUVIYEA-UHFFFAOYSA-N 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 230000005496 eutectics Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 239000008172 hydrogenated vegetable oil Substances 0.000 description 1
- 229920013821 hydroxy alkyl cellulose Polymers 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 229940119170 jojoba wax Drugs 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- HGPXWXLYXNVULB-UHFFFAOYSA-M lithium stearate Chemical compound [Li+].CCCCCCCCCCCCCCCCCC([O-])=O HGPXWXLYXNVULB-UHFFFAOYSA-M 0.000 description 1
- SZINCDDYCOIOJQ-UHFFFAOYSA-L manganese(2+);octadecanoate Chemical compound [Mn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O SZINCDDYCOIOJQ-UHFFFAOYSA-L 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 238000003359 percent control normalization Methods 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000003923 scrap metal Substances 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000005029 sieve analysis Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- PTISTKLWEJDJID-UHFFFAOYSA-N sulfanylidenemolybdenum Chemical class [Mo]=S PTISTKLWEJDJID-UHFFFAOYSA-N 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 150000003658 tungsten compounds Chemical class 0.000 description 1
- 238000007514 turning Methods 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 238000009692 water atomization Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Images
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
- B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
-
- 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
Definitions
- the present invention relates to improved iron-based metallurgical powder compositions and methods of making and using the same.
- the iron-based powder compositions contain a mixture of substantially pure iron powder and an iron-alloy powder that preferably contains molybdenum as an alloying additive.
- the iron-based powder compositions thus produced have improved machinability when formed into metal parts.
- metal powder compositions are typically formed from metal-based powders and other additives such as lubricants, and binders.
- the metal-based powders are typically iron powders that optionally may be alloyed with one or more alloying components.
- a common technique for preparing an iron-alloy powder is to form a homogeneous molten metal composition containing iron and one or more desired alloying components, and water atomizing the molten metal composition to form a homogeneous powder composition.
- the metal-based powder after any optional alloying, is often mixed with other additives to improve the properties of the final part.
- the metal-based powder is often admixed with at least one other alloying additive that is in powder form (“alloying powder”).
- alloying powder permits, for example, the attainment of higher strength and other mechanical properties in the final sintered part.
- the mixture of metal-based powder and optional alloying powders are often also mixed with other additives such as lubricants and binding agents to form the final metal powder composition.
- This metal powder composition is typically poured into a compaction die and compacted under pressure (e.g., 5 to 70 tons per square inch (tsi)), and in some circumstances at elevated temperatures, to form the compacted, or “green” part.
- the green part is then usually sintered to form a cohesive metallic part and optionally finished. Examples of types of finishing steps include machining the metal part (e.g., cutting, shaving, drilling, turning, milling, etc.) to the desired specifications.
- metal parts are often difficult to machine.
- a metal part may be difficult to drill, leading to longer machining time, decrease in the life of the machine tool, and increased energy usage to operate the machining equipment.
- Schmidt discloses that the machinability of an iron-based metal part can be improved through the use of a steel powder mixture of graphite and an iron-molybdenum-manganese alloy. The steel powder after compaction and sintering is heated and cooled according to certain temperature profiles to improve the machinability of the metal part.
- Uenosono discloses a metal powder containing a mixture of iron powder having less than 0.1 weight percent manganese and from about 0.08 weight percent to about 0.15 weight percent sulfur; graphite; and from about 0.05 to about 0.70 weight percent of at least one compound selected from MoO 3 or WO 3 .
- the iron powder is disclosed to have excellent machinability and high strength due to the dissolution of molybdenum or tungsten compounds in the ferrite particles upon sintering of the compacted metal part in a hydrogen-containing atmosphere.
- Kaneko discloses a sintered material having good machinability, where the sintered material is prepared by compacting and sintering a powder containing a mixture of composite oxide of CaO—MgO—SiO 2 and an iron dominant metal matrix.
- the iron dominant metal matrix may be prepared from a mixture of pure iron and “hard” particles of FeMo, FeCr, FeW, or Tribaloy (containing Co—Ho—Cr and/or Co—Ho—Si). These hard particles are believed to contain at least 50 weight percent of the non-iron elements to provide the desired hardness.
- compositions and/or methods provide ways of improving the machinability of a metal part
- such alternate compositions and methods would result in metal parts having comparable or improved machinability.
- the present invention provides metallurgical powder compositions and methods of making and using the same.
- the metallurgical powder compositions when formed into metal parts, exhibit improved machinability. This improved machinability is at least in part due to the presence of certain amounts of at least one iron-alloy powder in the metallurgical powder compositions.
- a method in one embodiment, includes providing an iron-alloy powder containing iron and at least one alloying additive, where the alloying additive is present in an amount of from about 0.01 weight percent to about 7.0 weight percent and the iron is present in an amount of at least 85 weight percent based on the total weight of the iron-alloy powder.
- Admixed with the iron-alloy powder is a substantially pure iron powder and carbon, typically a carbon powder, to form the metallurgical powder composition.
- the metallurgical powder composition preferably contains from about 5 weight percent to about 40 weight percent of the iron-alloy powder, at least 55 percent by weight of the iron powder, and at least 0.1 weight percent carbon based on the total weight of the metallurgical powder composition.
- a metallurgical powder composition contains from about 5 weight percent to about 40 weight percent of an iron-molybdenum alloy powder containing iron and molybdenum, where the amount of molybdenum is from about 0.10 weight percent to about 7.0 weight percent and the amount of iron is at least 85 weight percent based on the weight of the iron-molybdenum alloy powder.
- the metallurgical powder composition also contains at least 55 weight percent of substantially pure iron powder, and from about 0.1 weight percent to about 3.0 weight percent carbon.
- the present invention also provides a method of forming a metal part that includes providing a metallurgical powder composition of the present invention and compacting the metallurgical powder composition at a pressure of at least about 5 tsi to form a metal part.
- FIG. 1 is a graph showing the mean thrust (in pounds) produced in drilling a metal part formed from an metallurgical powder composition of the present invention (Example 5) in comparison to metal parts made from metallurgical powder compositions containing no iron-alloy powder (Comparative Examples 1 and 2).
- the present invention provides improved metallurgical powder compositions that when formed into metal parts have improved machinability.
- machinability it is meant the ability of a metal part to be finished in some manner by machine operated tools.
- metal parts produced in accordance with the methods of the present invention are preferably capable of being shaped, shaved, drilled, cut, turned, milled, or any combination thereof.
- the metallurgical powder compositions of the present invention are iron- based powder compositions containing substantially pure iron powder, an iron-alloy powder, and carbon. These metallurgical powder compositions may also optionally contain alloying powders, one or more lubricants, one or more binders, any other conventional powder metallurgy additive, or any combination thereof.
- the iron-alloy powder useful in the present invention is preferably made by partially or completely alloying iron with at least one alloying additive (for example, molybdenum containing compounds) that can provide a hard phase for improving machinability.
- alloying additive for example, molybdenum containing compounds
- alloying it is meant that the alloying additives and iron are admixed in a manner to permit melting, diffusion bonding or chemical bonding of the iron and alloying additive. Suitable processes for alloying include for example “prealloying” and “diffusion bonding.”
- Prealloyed and diffusion bonded iron-alloy powder may be made according to any technique known to those skilled in the art.
- prealloyed iron-alloy powder can be prepared from a melt of iron and one or more desired alloying additives. Preferably, the melt is then atomized so that the atomized droplets form a powder upon solidification.
- Diffusion bonded iron-alloy powder can be prepared for example by blending iron powder with one or more alloying additives, preferably in oxide form, and annealing the resulting mixture at high temperatures (e.g., about 800 ° C. or greater). During annealing, the alloying compounds diffuse and partially alloy into the outer surfaces of the iron particles.
- a preferred diffusion bonding process is disclosed in GB 1,162,702, which is hereby incorporated by reference in its entirety.
- the iron-alloy powder is formed by a prealloying process.
- Prealloying has the advantage of facilitating complete alloying of the iron and alloying additives.
- the iron-alloy powder is present in the metallurgical powder composition at a concentration that is effective in improving the machinability of the metal part in comparison to a composition containing no iron-alloy powder.
- the amount of iron-alloy powder is from about 5 weight percent to about 40 weight percent, more preferably from about 10 weight percent to about 30 weight percent, and most preferably from about 12 weight percent to about 20 weight percent, based on the total weight of the metallurgical powder composition.
- Iron that can be used to form the iron-alloy powder is preferably substantially pure iron containing not more than about 1.0% by weight, preferably no more than about 0.5% by weight, of normal impurities.
- the iron may be in any physical form prior to prealloying.
- the iron may be in powder form or in the form of scrap metal.
- the iron is preferably in powder form.
- suitable alloying additives for forming the iron-alloy powder include, but are not limited to elements, compounds, or alloys of molybdenum, manganese, magnesium, tungsten, chromium, silicon, copper, nickel, gold, vanadium, columbium (niobium), or aluminum, or oxides thereof; binary alloys of copper and tin or phosphorus; carbides of tungsten or silicon; silicon nitride; sulfides of manganese or molybdenum, or combinations thereof.
- the iron-alloy powder contains at least one alloying additive containing molybdenum, manganese, magnesium, tungsten, chromium, silicon, copper, nickel, vanadium, oxides thereof, or any combination thereof, and more preferably molybdenum, chromium, vanadium, tungsten, or combinations thereof.
- the total amount of alloying additive in the iron-alloy powder will depend upon the alloying additive(s) chosen. Typically, the alloying additives are present in the iron-alloy powder in an amount of from about 0.01 weight percent to about 7.0 weight percent, preferably from about 0.10 weight percent to about 3.0 weight percent, and most preferably from about 0.10 weight percent to about 2.0 weight percent, based on the total weight of the iron-alloy powder.
- the iron-alloy powder may also contain residual impurities, such as from the iron used to form the iron-alloy powder.
- the iron-alloy powder contains minimum residual impurities of at least about 0.15 weight percent and more preferably of at least about 0.25 weight percent, and preferably contains maximum residual impurities of up to about 1.0 weight percent, and more preferably up to about 0.9 weight percent, based on the total weight of the iron-alloy powder.
- the balance of the iron-alloy powder is preferably iron. Iron is preferably present in the iron-alloy powder in an amount of at least 85.0 weight percent, more preferably at least about 90.0 weight percent, and most preferably from about 94.0 weight percent to about 99.8 weight percent.
- the iron is prealloyed with at least one alloying additive that contains molybdenum to form an iron-molybdenum prealloy powder.
- Molybdenum additive useful in forming an iron-molybdenum prealloy powder is any element, compound, or alloy that contains molybdenum and is capable of alloying with iron in the prealloying process.
- the molybdenum additive may be, for example, an oxide of molybdenum such as molybdenum trioxide or a ferromolybdenum alloy.
- the molybdenum additive may also be substantially pure elemental molybdenum (preferably having a purity of greater than about 90 wt %).
- the molybdenum additive is an oxide of molybdenum such as molybdenum trioxide.
- the iron-molybdenum prealloy powder preferably contains from about 0.40 weight percent to about 1.6 weight percent molybdenum, based on the total weight of the iron-molybdenum prealloy powder, and from about 97.4 weight percent to about 99.50 weight percent iron.
- the iron-molybdenum prealloy powder preferably contains maximum residual impurities of about 0.03 weight percent sulfur, about 0.02 weight percent silicon, and about 0.01 weight percent nitrogen based on the total weight of the prealloy powder.
- iron-molybdenum prealloy powders commercially available include Hoeganaes' ANCORSTEEL 150HP steel powder, 85 HP steel powder, 50HP steel powder, or combinations thereof.
- the amounts of molybdenum in the 150 HP, 85HP, and 50 HP steel powders are respectively about 1.5 weight percent, 0.85 weight percent, and 0.55 weight percent based on the total weight of the prealloy.
- These iron-molybdenum prealloy powders contain less than about 0.75 weight percent of materials such as manganese, chromium, silicon, copper, nickel, or aluminum, and less than about 0.02 weight percent carbon, with the balance being substantially iron.
- iron-molybdenum prealloy powder is Hoeganaes' ANCORSTEEL 4600V steel powder, which contains about 0.5-0.6 weight percent molybdenum, about 1.5-2.0 weight percent nickel, about 0.1-0.25 weight percent manganese, less than about 0.02 weight percent carbon, and the balance preferably being substantially iron.
- Other ANCORSTEEL iron-molybdenum prealloy powders that are useful in the present invention include for example ANCORSTEEL 2000 and 737 steel powders. The 150HP, 85HP, or 50HP steel powders are preferred for use as the prealloy powder in the present invention.
- the metallurgical powder compositions of the present invention also contain substantially pure iron powder.
- the substantially pure iron powder is present in the metallurgical powder composition in an amount of at least about 55 weight percent, more preferably from about 60 weight percent to about 95 weight percent, and most preferably from about 70 weight percent to about 90 weight percent, based on the total weight of the metallurgical powder composition.
- Substantially pure iron powder that can be used in the invention are powders of iron preferably containing not more than about 1.0% by weight, more preferably no more than about 0.5% by weight, of normal impurities.
- Examples of such highly compressible, metallurgical-grade iron powders are the ANCORSTEEL 1000 series of pure iron powders, e.g. 1000, 1000B, and 1000C, available from Hoeganaes Corporation, Riverton, N.J.
- ANCORSTEEL 1000 iron powder has a typical screen profile of about 22% by weight of the particles below a No. 325 sieve (U.S. series) and about 10% by weight of the particles larger than a No. 100 sieve with the remainder between these two sizes (trace amounts larger than No. 60 sieve).
- the ANCORSTEEL 1000 powder has an apparent density of from about 2.85-3.00 g/cm 3 , typically 2.94 g/cm 3 .
- the particles of iron-alloy powder and substantially pure iron powder have a distribution of particle sizes.
- these powders are such that at least about 90% by weight of the powder sample can pass through a No. 45 sieve (U.S. series), and more preferably at least about 90% by weight of the powder sample can pass through a No. 60 sieve.
- These powders typically have at least about 50% by weight of the powder passing through a No. 70 sieve and retained above or larger than a No. 400 sieve, more preferably at least about 50% by weight of the powder passing through a No. 70 sieve and retained above or larger than a No. 325 sieve.
- these powders typically have at least about 5 weight percent, more commonly at least about 10 weight percent, and generally at least about 15 weight percent of the particles passing through a No. 325 sieve.
- these powders can have a weight average particle size as small as one micron or below, or up to about 850-1,000 microns, but generally the particles will have a weight average particle size in the range of about 10-500 microns.
- Preferred are iron-alloy particles or substantially pure iron particles having a maximum weight average particle size up to about 350 microns; more preferably the particles will have a weight average particle size in the range of about 25-150 microns, and most preferably 80-150 microns. Reference is made to MPIF Standard 05 for sieve analysis.
- the metallurgical powder composition also preferably contains carbon.
- the carbon is preferably added as a substantially pure carbon powder, such as graphite.
- the carbon powder has a purity of at least about 99.0 weight percent and more preferably a purity of at least about 99.5 weight percent.
- the carbon powder may be in crystalline and/or amorphous form.
- Carbon is preferably present in the metallurgical powder composition in an amount of from about 0.1 weight percent to about 3.0 weight percent, more preferably from about 0.2 weight percent to about 2.0 weight percent, and most preferably from about 0.3 weight percent to about 1.2 weight percent, based on the weight of the metallurgical powder composition.
- the metallurgical powder compositions of the present invention may also optionally contain alloying powders in addition to the carbon powder.
- alloying powder refers to any particulate element, compound, or alloy powder physically blended with the metallurgical powder composition, whether or not that additive ultimately alloys or partially alloys with the metallurgical powder composition.
- Examples of optional alloying powders that may be present in the metallurgical powder composition include elements, compounds, or alloys containing molybdenum, manganese, copper, nickel, chromium, silicon, gold, vanadium, columbium (niobium), phosphorus, aluminum, boron, or oxides thereof; binary alloys of copper and tin, copper and nickel, or copper and phosphorous; ferro-alloys of manganese, chromium, boron, phosphorus, or silicon; low melting ternary and quaternary eutectics of carbon in combination with elements selected from iron, vanadium, manganese, chromium, molybdenum or combinations thereof; carbides of tungsten or silicon; silicon nitride; aluminum oxide; and sulfides of manganese or molybdenum, and combinations thereof.
- Preferred alloying powders include elements, compounds, or alloys containing molybdenum, manganese, copper, nickel, chromium, vanadium, phosphorus, or combinations thereof, and more preferably elements, compounds, or alloys containing copper, nickel, or combinations thereof.
- the alloying powders are preferably present in the metallurgical powder composition in amounts of up to about 10 weight percent, and typically in the range of from about 0.25 to about 10 weight percent, preferably from about 0.25 to about 7 weight percent, and more preferably from about 0.5 to about 5 weight percent.
- the alloying powders generally have a weight average particle size below about 100 microns, preferably below about 75 microns, more preferably below about 30 microns, and most preferably in the range of about 5 microns to about 20 microns.
- the particle size of the alloying powders is generally relatively small and can be analyzed by laser light scattering technology as opposed to screening techniques.
- Laser light scattering technology reports the particle size distribution in d x values, where it is said that “x” percent by volume of the powder has a diameter below the reported value.
- the alloying particles generally have a particle size distribution such that they have a d 90 value of below about 100 microns, preferably below about 75 microns, and more preferably below about 50 microns; and a d 50 value of below about 75 microns, preferably below about 50 microns, and more preferably below about 30 microns.
- the metallurgical powder composition contains an alloying powder containing copper.
- the copper provides hardenability properties to metal parts formed from the metallurgical powder compositions.
- the copper containing powder is preferably elemental copper having relatively few impurities.
- the copper containing powder contains at least 90 weight percent, more preferably at least 98 weight percent, and most preferably at least 99.5 weight percent copper based on the total weight of the copper containing powder.
- the amount of copper containing powder present in the metallurgical powder composition of the present invention is such that there is at least 0.2 weight percent, more preferably from about from about 0.5 weight percent to about 4.0 weight percent, and most preferably from about 1.0 to about 3.0 weight percent elemental copper, based on the total weight of the metallurgical powder composition.
- the metallurgical powder compositions of the present invention may also include any special-purpose additive commonly used with metallurgical composition such as lubricants, machining agents, and plasticizers.
- the metallurgical powder composition contains a lubricant to reduce the ejection force required to remove a compacted part from the die cavity.
- a lubricant to reduce the ejection force required to remove a compacted part from the die cavity.
- typical powder metallurgy lubricants include the stearates, such as zinc stearate, lithium stearate, manganese stearate, or calcium stearate; synthetic waxes, such as ethylene bisstearamide or polyolefins; or combinations thereof.
- the lubricant may also be a polyamide lubricant, such as PROMOLD-450, disclosed in U.S. Pat. No. 5,368,630, particulate ethers disclosed in U.S. Pat. No.
- the lubricant may also be a combination of any of the aforementioned lubricants described above.
- the lubricant is generally added in an amount of up to about 2.0 weight percent, preferably from about 0.1 to about 1.5 weight percent, more preferably from about 0.1 to about 1.0 weight percent, and most preferably from about 0.2 to about 0.75 weight percent, of the metallurgical powder composition.
- Preferred lubricants are ethylene bisstearamide, zinc stearate, KenolubeTM (supplied by Hoganas Corporation, located in Hoganas, Sweden), FerrolubeTM (supplied by Blanchford), and polyethylene wax.
- these lubricants are added in an amount of from about 0.2 weight percent to about 1.5 weight percent based on the total weight of the metallurgical powder composition formed.
- additives may also be present in the metallurgical powder compositions, such as plasticizers and machining agents.
- these other additives are present in the metallurgical powder composition in an amount of from about 0.05 weight percent to about 1.5 weight percent, and more preferably from about 0.1 weight percent to about 0.5 weight percent based on the total weight of the metallurgical powder composition.
- Plasticizers such as polyethylene-polypropylene copolymer, are typically used in connection with binders and/or lubricants.
- Machining agents such as molybdenum sulfides, iron sulfides, boron nitride, boric acid, or combinations thereof are typically used to aid in final machining operations.
- manganese sulfide is present in the metallurgical powder composition in an amount of from about 0.1 weight percent to about 0.75 weight percent based on the weight of the metallurgical powder composition.
- the metallurgical powder composition may also contain one or more binding agents to bond the different components present in the metallurgical powder compostion so as to inhibit segregation.
- binding as used herein, it is meant any physical or chemical method that facilitates adhesion of the components of the metallurgical powder composition.
- binding agent that can be used in the present invention are those commonly employed in the powder metallurgical arts. Examples of such binding agents are found in U.S. Pat. No. 4,834,800 to Semel, U.S. Pat. No. 4,483,905 to Engstrom, U.S. Pat. No. 5,154,881 to Rutz et al., and U.S. Pat. No. 5,298,055 to Semel et.al., the disclosures of which are hereby incorporated by reference in their entireties.
- binding agents include, for example, polyglycols such as polyethylene glycol or polypropylene glycol; glycerine; polyvinyl alcohol; homopolymers or copolymers of vinyl acetate; cellulosic ester or ether resins; methacrylate polymers or copolymers; alkyd resins; polyurethane resins; polyester resins; or combinations thereof.
- polyglycols such as polyethylene glycol or polypropylene glycol
- glycerine polyvinyl alcohol
- homopolymers or copolymers of vinyl acetate cellulosic ester or ether resins
- methacrylate polymers or copolymers alkyd resins
- polyurethane resins polyester resins
- binding agents include, for example, polyglycols such as polyethylene glycol or polypropylene glycol; glycerine; polyvinyl alcohol; homopolymers or copolymers of vinyl acetate; cellulosic ester or ether resin
- Useful binding agents also include the dibasic organic acid, such as azelaic acid, and one or more polar components such as polyethers (liquid or solid) and acrylic resins as disclosed in U.S. Pat. No. 5,290,336 to Luk, which is incorporated herein by reference in its entirety.
- the binding agents in the '336 Patent to Luk can also advantageously act as lubricants.
- Additional useful binding agents include the cellulose ester resins, hydroxy alkylcellulose resins, and thermoplastic phenolic resins described in U.S. Pat. No. 5,368,630 to Luk, which is incorporated herein by reference in its entirety.
- the binding agent can further be the low melting, solid polymers or waxes, e.g., a polymer or wax having a softening temperature of below 200° C. (390° F.), such as polyesters, polyethylenes, epoxies, urethanes, paraffins, ethylene bisstearamides, and cotton seed waxes, and also polyolefins with weight average molecular weights below 3,000, and hydrogenated vegetable oils that are C 14-24 alkyl moiety triglycerides and derivatives thereof, including hydrogenated derivatives, e.g. cottonseed oil, soybean oil, jojoba oil, and blends thereof, as described in WO 99/20689, published Apr.
- a polymer or wax having a softening temperature of below 200° C. (390° F.) such as polyesters, polyethylenes, epoxies, urethanes, paraffins, ethylene bisstearamides, and cotton seed waxes, and also polyolefin
- binding agents can be applied by the dry bonding techniques discussed in that application and in the general amounts set forth above for binding agents.
- Further binding agents that can be used in the present invention are polyvinyl pyrrolidone as disclosed in U.S. Pat. No. 5,069,714, which is incorporated herein in its entirety by reference, or tall oil esters.
- Preferred binding agents are polyethylene oxide and polyvinylacetate, or combinations thereof, which are binding agents disclosed in WO 99/20689,
- the amount of binding agent present in the metallurgical powder composition depends on such factors as the density, particle size distribution and amounts of the iron-alloy powder, the iron powder and optional alloying powder in the metallurgical powder composition. Generally, the binding agent will be added in an amount of at least about 0.005 weight percent, more preferably from about 0.005 weight percent to about 2 weight percent, and most preferably from about 0.05 weight percent to about 1 weight percent, based on the total weight of the metallurgical powder composition.
- the metallurgical powder composition contains from about 10 weight percent to about 20 weight percent of an iron-molybdenum prealloy powder, from about 80 weight percent to about 90 weight percent substantially pure iron powder, from about 0.1 weight percent to about 1.2 weight percent carbon that is preferably graphite powder, and from about 0.1 to about 3.0 weight percent of copper that is preferably in the form of a copper containing powder.
- the iron-molybdenum prealloy powder preferably contains from about 0.4 weight percent to about 2.0 weight percent molybdenum and from about 98 weight percent to about 99.6 weight percent iron.
- the percentages of iron, molybdenum, carbon and copper in the metallurgical powder composition can be determined for example by an elemental analysis.
- the present invention also provides methods of preparing metallurgical powder compositions.
- an iron-alloy powder that has preferably been prepared in accordance with the methods as previously described herein is provided.
- the iron-alloy powder is admixed with substantially pure iron powder and preferably carbon powder, in the amounts previously described herein, to form the metallurgical powder compositions of the present invention.
- other additives can be added to the metallurgical powder composition in the amounts previously described herein. For example, any combination of alloying powders, lubricants, binding agents, machining agents, plasticizers, or any other conventional metallurgical powder additive may be added.
- the method of combining the iron-alloy powder, the substantially pure iron powder, the carbon powder, and other desired additives may be performed according to any technique well known to those skilled in the art.
- the method used results in a uniformly mixed metallurgical powder composition that does not readily segregate.
- the order of addition of the iron-alloy powder, the substantially pure iron powder, the carbon powder, and other desired additives is not critical.
- the order of addition is in a manner to achieve a uniform mixture of the metallurgical powder composition.
- the methods of the present invention include adding a binding agent to the metallurgical powder composition to bond the iron-alloy powder, the substantially pure iron powder and other additives to inhibit segregation.
- the binding agent can be added to the powder mixture according to any technique known to those skilled in the art. For example, the procedures taught by U.S. Pat. Nos. 4,834,800 to Semel; 4,483,905 to Engstrom; 5,154,881 to Rutz et al.; and 5,298,055 to Semel et al.; and WO 99/20689, published Apr. 29, 1999, can be used, the disclosures of which are hereby incorporated by reference in their entireties.
- the binding agent is added in a liquid form and mixed with the powders until good wetting of the powders is attained.
- Those binding agents that are in liquid form at ambient conditions can be added to the powder as such, but it is preferred that the binding agent, whether liquid or solid, be dissolved or dispersed in an organic solvent and added as a liquid solution, thereby providing substantially homogeneous distribution of the binding agent throughout the mixture.
- the wet powder is thereafter processed using conventional techniques to remove the solvent. Typically, if the mixes are small, generally 5 lbs. or less, the wet powder is spread over a shallow tray and allowed to dry in air. On the other hand, in the case of larger mixes, the drying step can be accomplished in the mixing vessel by employing heat and vacuum.
- the sequence of addition of the binding agent and a lubricant can be varied to alter the final characteristics of the metallurgical powder composition.
- the procedures taught in U.S. Pat. No. 5,256,185 to Semel et al., which is hereby incorporated by reference in its entirety can be used.
- the lubricant can be blended with the iron-alloy powder, the substantially pure iron powder, the carbon powder, the alloying powders and other optional additives, and then, subsequently, the binding agent is applied to that composition.
- a portion of the lubricant preferably from about 50 to about 99 weight percent, more preferably from about 75 to about 95 weight percent, is added to a mixture of the iron-alloy powder, the substantially pure iron powder, and other additives, then the binding agent is added, followed by removal of the solvent, and subsequently the rest of the lubricant is added to the metal powder composition.
- One further method is to add the binding agent first to a mixture of the iron-alloy powder and other additives, remove the solvent, and subsequently add the entire amount of the lubricant.
- metallurgical powder compositions of the present invention thus formed can be compacted in a die according to standard metallurgical techniques to form metal parts.
- Typical compaction pressures range between about 5 and 200 tons per square inch (tsi) (69-2760 MPa), preferably from about 20-100 tsi (276-1379 MPa), and more preferably from about 25-60 tsi (345-828 MPa).
- the part can be sintered, according to standard metallurgical techniques at temperatures, sintering times, and other conditions appropriate to the metallurgical powder composition.
- sintering temperatures range from about 1900° F. to about 2400° F. and are conducted for a time sufficient to achieve metallurgical bonding and alloying.
- the metallurgical powder composition may also be double pressed and double sintered by techniques well known to those skilled in the art.
- Metal parts of various shapes and for various uses may be formed from the metallurgical powder compositions of the present invention.
- the metal parts may be shaped for use in the automotive, aerospace, or nuclear energy industries.
- the metallurgical powder compositions made in accordance with the methods of the present invention have unexpectedly superior machinability properties. These improvements are especially observed when the metallurgical powder composition contains from about 10 weight percent to about 30 weight percent of an iron-molybdenum prealloy powder, from about 70 weight percent to about 90 weight percent of a substantially pure iron powder, from about 0.1 weight percent to about 3.0 weight percent of a carbon powder, and from about 0.1 weight percent to about 3.0 weight percent of a copper containing powder.
- the iron molybdenum prealloy contains from about 0.40 to about 2.0 weight percent molybdenum and from about 98 weight percent to about 99.6 weight percent iron.
- the machinability can be further enhanced through the presence of a machining agent such as manganese sulfide in the metallurgical powder composition.
- Iron-based metallurgical powder compositions were prepared in accordance with the methods of the present invention. Comparative metal powder compositions were also prepared. The powder compositions prepared were compacted and sintered to form metal parts and evaluated for machinability.
- Metallurgical powder compositions having the compositions shown in Table 1 were prepared. TABLE 1 Composition of Metal Powders Tested Fe Fe-Alloy Carbon Cu MnS Lubricant Examples Powder Powder, wt % wt % wt % wt % wt % Control Balance 0.0 0.5 2.0 0.0 0.0 Comp. Ex. Balance 0.0 0.6 1.75 0.0 0.75 1 Comp. Ex.
- compositions were prepared by uniformly blending all the ingredients in the amounts shown in Table 1.
- the iron powder used in all examples was Ancorsteel 1000A available from Hoeganaes Corporation, located in Cinnaminson, N.J.
- the iron-alloy powder used in all examples was AncorsteelTM 85HP steel powder also available from Hoeganaes Corporation.
- Ancorsteel 85HP is an iron-molybdenum prealloy powder containing about 0.85 weight percent molybdenum.
- the graphite used in all examples (shown as “Carbon” in Table 1) had a weight average particle size of about 6 to 8 microns and was obtained from Asbury Graphite Mills, Inc., located in Asbury, N.J.
- the copper powder (shown as “Cu” in Table 1) used in all examples was Accupowder from Accupowder Corporation.
- the copper powder had a weight average particle size of from about 10 microns to about 14 microns and a purity of 99.5 weight percent.
- the “MnS” shown in Table 1 is manganese sulfide, a machining agent.
- the lubricant shown in Table 1 was AcrawaxTM C lubricant.
- Acrawax C is a synthetic wax and was obtained from Algroup Lonza located in Fair Lawn, N.J.
- each of the metallurgical powder compositions in Table 1 were compacted into 4 inch diameter by 1 inch thick discs having a density of 6.8 g/cm 3 .
- the discs were sintered at 2050° F. for 30 minutes in an atmosphere of 10% hydrogen and 90% nitrogen and allowed to cool to ambient temperature.
- each drill bit was calibrated in the following manner. Twenty drill bits of 0.25 inch diameter were used to drill 0.95 inch deep holes in discs formed from the “Control” powder shown in Table 1. Each drill bit was used to drill approximately 2 to 3 holes for a total of about 40 to about 60 holes. The holes were drilled at a feed rate of 0.005 inches per revolution and a cutting speed of 2220 rpm. During drilling the drill torque and drill thrust were measured automatically for each drill bit, and an average drill torque and thrust were calculated from all measurements. Only drill bits having a drill torque and thrust within ⁇ 5 percent of the average were used in the machinability tests.
- the mean thrust was the mean value of thrust for all holes drilled prior to failure of the drill bit.
- Table 2 also shows the number of holes drilled to failure that was used for calculating the mean thrust. The number of holes drilled to failure depended in part on the strength of the material (increasing the strength decreases the number of holes to failure).
- Example 10 40.0 476 131.0
- the results in Table 2 show that the addition of the iron-alloy powder in an metallurgical powder composition reduces the mean thrust of a drill bit during the drilling of a disc.
- the mean thrust can be reduced somewhat by the addition of manganese sulfide to an iron based powder composition (see comparative Example 1 in comparison to Comparative Example 2), further improvement can be achieved by addition of a iron-alloy powder.
- the results for mean thrust obtained for Comparative Examples 1 to 2 and Example 5 are shown in FIG. 1.
- FIG. 1 is a bar graph showing mean thrust for discs prepared from Comparative Examples 1 to 2 and Example 5.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Powder Metallurgy (AREA)
- Treatment Of Steel In Its Molten State (AREA)
Abstract
The present invention provides iron-based metallurgical powder compositions and a method of making and using the same. The metallurgical powder compositions of the present invention contain certain amounts of an iron-alloy powder having iron and at least one alloying additive; substantially pure iron powder; and a carbon powder, such as graphite. The metallurgical powder compositions are prepared by admixing the iron-alloy powder with the iron powder and carbon powder. The metallurgical powder compositions thus produce and when formed into metal parts have, for example, improved machinability properties.
Description
- The present invention relates to improved iron-based metallurgical powder compositions and methods of making and using the same. The iron-based powder compositions contain a mixture of substantially pure iron powder and an iron-alloy powder that preferably contains molybdenum as an alloying additive. The iron-based powder compositions thus produced have improved machinability when formed into metal parts.
- Industrial usage of metal parts manufactured by the compaction and sintering of metal powder compositions is expanding rapidly into a multitude of areas. In the manufacture of such parts, metal powder compositions are typically formed from metal-based powders and other additives such as lubricants, and binders. The metal-based powders are typically iron powders that optionally may be alloyed with one or more alloying components.
- A common technique for preparing an iron-alloy powder is to form a homogeneous molten metal composition containing iron and one or more desired alloying components, and water atomizing the molten metal composition to form a homogeneous powder composition.
- The metal-based powder, after any optional alloying, is often mixed with other additives to improve the properties of the final part. For example, the metal-based powder is often admixed with at least one other alloying additive that is in powder form (“alloying powder”). The alloying powder permits, for example, the attainment of higher strength and other mechanical properties in the final sintered part.
- The mixture of metal-based powder and optional alloying powders are often also mixed with other additives such as lubricants and binding agents to form the final metal powder composition. This metal powder composition is typically poured into a compaction die and compacted under pressure (e.g., 5 to 70 tons per square inch (tsi)), and in some circumstances at elevated temperatures, to form the compacted, or “green” part. The green part is then usually sintered to form a cohesive metallic part and optionally finished. Examples of types of finishing steps include machining the metal part (e.g., cutting, shaving, drilling, turning, milling, etc.) to the desired specifications.
- One problem that occurs in the finishing of metal parts is that the metal parts are often difficult to machine. For example, a metal part may be difficult to drill, leading to longer machining time, decrease in the life of the machine tool, and increased energy usage to operate the machining equipment.
- One solution to increasing the machinability of iron-based metal parts is disclosed in U.S. Pat. No. 4,018,632 to Schmidt(hereinafter “Schmidt”). Schmidt discloses that the machinability of an iron-based metal part can be improved through the use of a steel powder mixture of graphite and an iron-molybdenum-manganese alloy. The steel powder after compaction and sintering is heated and cooled according to certain temperature profiles to improve the machinability of the metal part.
- Another solution for increasing the machinability of iron-based metal parts is disclosed in U.S. Pat. No. 5,599,377 to Uenosono et al. (hereinafter “Uenosono”). Uenosono discloses a metal powder containing a mixture of iron powder having less than 0.1 weight percent manganese and from about 0.08 weight percent to about 0.15 weight percent sulfur; graphite; and from about 0.05 to about 0.70 weight percent of at least one compound selected from MoO3 or WO3. The iron powder is disclosed to have excellent machinability and high strength due to the dissolution of molybdenum or tungsten compounds in the ferrite particles upon sintering of the compacted metal part in a hydrogen-containing atmosphere.
- Another solution proposed for improving the machinability of metal parts is disclosed in U.S. Pat. No. 5,679,909 to Kaneko et al. (hereinafter “Kaneko”). Kaneko discloses a sintered material having good machinability, where the sintered material is prepared by compacting and sintering a powder containing a mixture of composite oxide of CaO—MgO—SiO2 and an iron dominant metal matrix. The iron dominant metal matrix may be prepared from a mixture of pure iron and “hard” particles of FeMo, FeCr, FeW, or Tribaloy (containing Co—Ho—Cr and/or Co—Ho—Si). These hard particles are believed to contain at least 50 weight percent of the non-iron elements to provide the desired hardness.
- Although the above compositions and/or methods provide ways of improving the machinability of a metal part, it would be desirable to develop alternate compositions and methods. Preferably such alternate compositions and methods would result in metal parts having comparable or improved machinability.
- The present invention provides metallurgical powder compositions and methods of making and using the same. The metallurgical powder compositions, when formed into metal parts, exhibit improved machinability. This improved machinability is at least in part due to the presence of certain amounts of at least one iron-alloy powder in the metallurgical powder compositions.
- In one embodiment of the present invention, a method is provided that includes providing an iron-alloy powder containing iron and at least one alloying additive, where the alloying additive is present in an amount of from about 0.01 weight percent to about 7.0 weight percent and the iron is present in an amount of at least 85 weight percent based on the total weight of the iron-alloy powder. Admixed with the iron-alloy powder is a substantially pure iron powder and carbon, typically a carbon powder, to form the metallurgical powder composition. The metallurgical powder composition preferably contains from about 5 weight percent to about 40 weight percent of the iron-alloy powder, at least 55 percent by weight of the iron powder, and at least 0.1 weight percent carbon based on the total weight of the metallurgical powder composition.
- In another embodiment of the present invention, a metallurgical powder composition is provided that contains from about 5 weight percent to about 40 weight percent of an iron-molybdenum alloy powder containing iron and molybdenum, where the amount of molybdenum is from about 0.10 weight percent to about 7.0 weight percent and the amount of iron is at least 85 weight percent based on the weight of the iron-molybdenum alloy powder. The metallurgical powder composition also contains at least 55 weight percent of substantially pure iron powder, and from about 0.1 weight percent to about 3.0 weight percent carbon.
- The present invention also provides a method of forming a metal part that includes providing a metallurgical powder composition of the present invention and compacting the metallurgical powder composition at a pressure of at least about 5 tsi to form a metal part.
- FIG. 1 is a graph showing the mean thrust (in pounds) produced in drilling a metal part formed from an metallurgical powder composition of the present invention (Example 5) in comparison to metal parts made from metallurgical powder compositions containing no iron-alloy powder (Comparative Examples 1 and 2).
- The present invention provides improved metallurgical powder compositions that when formed into metal parts have improved machinability. By “machinability” it is meant the ability of a metal part to be finished in some manner by machine operated tools. For example, metal parts produced in accordance with the methods of the present invention are preferably capable of being shaped, shaved, drilled, cut, turned, milled, or any combination thereof.
- The metallurgical powder compositions of the present invention are iron- based powder compositions containing substantially pure iron powder, an iron-alloy powder, and carbon. These metallurgical powder compositions may also optionally contain alloying powders, one or more lubricants, one or more binders, any other conventional powder metallurgy additive, or any combination thereof.
- It has been unexpectedly found that the machinability of iron-based metal parts can be significantly improved through the addition of certain amounts of iron-alloy powder in the metallurgical powder composition used to form the metal part. The iron-alloy powder useful in the present invention is preferably made by partially or completely alloying iron with at least one alloying additive (for example, molybdenum containing compounds) that can provide a hard phase for improving machinability.
- By “alloying” it is meant that the alloying additives and iron are admixed in a manner to permit melting, diffusion bonding or chemical bonding of the iron and alloying additive. Suitable processes for alloying include for example “prealloying” and “diffusion bonding.”
- Prealloyed and diffusion bonded iron-alloy powder may be made according to any technique known to those skilled in the art. For example, prealloyed iron-alloy powder can be prepared from a melt of iron and one or more desired alloying additives. Preferably, the melt is then atomized so that the atomized droplets form a powder upon solidification. Diffusion bonded iron-alloy powder can be prepared for example by blending iron powder with one or more alloying additives, preferably in oxide form, and annealing the resulting mixture at high temperatures (e.g., about 800 ° C. or greater). During annealing, the alloying compounds diffuse and partially alloy into the outer surfaces of the iron particles. A preferred diffusion bonding process is disclosed in GB 1,162,702, which is hereby incorporated by reference in its entirety.
- In a preferred embodiment of the present invention the iron-alloy powder is formed by a prealloying process. Prealloying has the advantage of facilitating complete alloying of the iron and alloying additives.
- Preferably, the iron-alloy powder is present in the metallurgical powder composition at a concentration that is effective in improving the machinability of the metal part in comparison to a composition containing no iron-alloy powder. Preferably, the amount of iron-alloy powder is from about 5 weight percent to about 40 weight percent, more preferably from about 10 weight percent to about 30 weight percent, and most preferably from about 12 weight percent to about 20 weight percent, based on the total weight of the metallurgical powder composition.
- Iron that can be used to form the iron-alloy powder is preferably substantially pure iron containing not more than about 1.0% by weight, preferably no more than about 0.5% by weight, of normal impurities. The iron may be in any physical form prior to prealloying. For example, the iron may be in powder form or in the form of scrap metal. For diffusion bonding, the iron is preferably in powder form.
- Examples of suitable alloying additives for forming the iron-alloy powder include, but are not limited to elements, compounds, or alloys of molybdenum, manganese, magnesium, tungsten, chromium, silicon, copper, nickel, gold, vanadium, columbium (niobium), or aluminum, or oxides thereof; binary alloys of copper and tin or phosphorus; carbides of tungsten or silicon; silicon nitride; sulfides of manganese or molybdenum, or combinations thereof. Preferably, the iron-alloy powder contains at least one alloying additive containing molybdenum, manganese, magnesium, tungsten, chromium, silicon, copper, nickel, vanadium, oxides thereof, or any combination thereof, and more preferably molybdenum, chromium, vanadium, tungsten, or combinations thereof.
- The total amount of alloying additive in the iron-alloy powder will depend upon the alloying additive(s) chosen. Typically, the alloying additives are present in the iron-alloy powder in an amount of from about 0.01 weight percent to about 7.0 weight percent, preferably from about 0.10 weight percent to about 3.0 weight percent, and most preferably from about 0.10 weight percent to about 2.0 weight percent, based on the total weight of the iron-alloy powder.
- The iron-alloy powder may also contain residual impurities, such as from the iron used to form the iron-alloy powder. Generally, the iron-alloy powder contains minimum residual impurities of at least about 0.15 weight percent and more preferably of at least about 0.25 weight percent, and preferably contains maximum residual impurities of up to about 1.0 weight percent, and more preferably up to about 0.9 weight percent, based on the total weight of the iron-alloy powder.
- The balance of the iron-alloy powder is preferably iron. Iron is preferably present in the iron-alloy powder in an amount of at least 85.0 weight percent, more preferably at least about 90.0 weight percent, and most preferably from about 94.0 weight percent to about 99.8 weight percent.
- In a preferred embodiment of the present invention, the iron is prealloyed with at least one alloying additive that contains molybdenum to form an iron-molybdenum prealloy powder. Molybdenum additive useful in forming an iron-molybdenum prealloy powder is any element, compound, or alloy that contains molybdenum and is capable of alloying with iron in the prealloying process. The molybdenum additive may be, for example, an oxide of molybdenum such as molybdenum trioxide or a ferromolybdenum alloy. The molybdenum additive may also be substantially pure elemental molybdenum (preferably having a purity of greater than about 90 wt %). Preferably, the molybdenum additive is an oxide of molybdenum such as molybdenum trioxide.
- In a most preferred embodiment of the present invention, the iron-molybdenum prealloy powder preferably contains from about 0.40 weight percent to about 1.6 weight percent molybdenum, based on the total weight of the iron-molybdenum prealloy powder, and from about 97.4 weight percent to about 99.50 weight percent iron. The iron-molybdenum prealloy powder preferably contains maximum residual impurities of about 0.03 weight percent sulfur, about 0.02 weight percent silicon, and about 0.01 weight percent nitrogen based on the total weight of the prealloy powder.
- Examples of suitable iron-molybdenum prealloy powders commercially available include Hoeganaes' ANCORSTEEL 150HP steel powder, 85 HP steel powder, 50HP steel powder, or combinations thereof. The amounts of molybdenum in the 150 HP, 85HP, and 50 HP steel powders are respectively about 1.5 weight percent, 0.85 weight percent, and 0.55 weight percent based on the total weight of the prealloy. These iron-molybdenum prealloy powders contain less than about 0.75 weight percent of materials such as manganese, chromium, silicon, copper, nickel, or aluminum, and less than about 0.02 weight percent carbon, with the balance being substantially iron. Another example of a commercially available iron-molybdenum prealloy powder is Hoeganaes' ANCORSTEEL 4600V steel powder, which contains about 0.5-0.6 weight percent molybdenum, about 1.5-2.0 weight percent nickel, about 0.1-0.25 weight percent manganese, less than about 0.02 weight percent carbon, and the balance preferably being substantially iron. Other ANCORSTEEL iron-molybdenum prealloy powders that are useful in the present invention include for example ANCORSTEEL 2000 and 737 steel powders. The 150HP, 85HP, or 50HP steel powders are preferred for use as the prealloy powder in the present invention.
- The metallurgical powder compositions of the present invention also contain substantially pure iron powder. Preferably, the substantially pure iron powder is present in the metallurgical powder composition in an amount of at least about 55 weight percent, more preferably from about 60 weight percent to about 95 weight percent, and most preferably from about 70 weight percent to about 90 weight percent, based on the total weight of the metallurgical powder composition.
- Substantially pure iron powder that can be used in the invention are powders of iron preferably containing not more than about 1.0% by weight, more preferably no more than about 0.5% by weight, of normal impurities. Examples of such highly compressible, metallurgical-grade iron powders are the ANCORSTEEL 1000 series of pure iron powders, e.g. 1000, 1000B, and 1000C, available from Hoeganaes Corporation, Riverton, N.J. For example, ANCORSTEEL 1000 iron powder, has a typical screen profile of about 22% by weight of the particles below a No. 325 sieve (U.S. series) and about 10% by weight of the particles larger than a No. 100 sieve with the remainder between these two sizes (trace amounts larger than No. 60 sieve). The ANCORSTEEL 1000 powder has an apparent density of from about 2.85-3.00 g/cm3, typically 2.94 g/cm3.
- The particles of iron-alloy powder and substantially pure iron powder have a distribution of particle sizes. Typically, these powders are such that at least about 90% by weight of the powder sample can pass through a No. 45 sieve (U.S. series), and more preferably at least about 90% by weight of the powder sample can pass through a No. 60 sieve. These powders typically have at least about 50% by weight of the powder passing through a No. 70 sieve and retained above or larger than a No. 400 sieve, more preferably at least about 50% by weight of the powder passing through a No. 70 sieve and retained above or larger than a No. 325 sieve. Also, these powders typically have at least about 5 weight percent, more commonly at least about 10 weight percent, and generally at least about 15 weight percent of the particles passing through a No. 325 sieve. As such, these powders can have a weight average particle size as small as one micron or below, or up to about 850-1,000 microns, but generally the particles will have a weight average particle size in the range of about 10-500 microns. Preferred are iron-alloy particles or substantially pure iron particles having a maximum weight average particle size up to about 350 microns; more preferably the particles will have a weight average particle size in the range of about 25-150 microns, and most preferably 80-150 microns. Reference is made to MPIF Standard 05 for sieve analysis.
- The metallurgical powder composition also preferably contains carbon. The carbon is preferably added as a substantially pure carbon powder, such as graphite. Preferably, the carbon powder has a purity of at least about 99.0 weight percent and more preferably a purity of at least about 99.5 weight percent. The carbon powder may be in crystalline and/or amorphous form. Carbon is preferably present in the metallurgical powder composition in an amount of from about 0.1 weight percent to about 3.0 weight percent, more preferably from about 0.2 weight percent to about 2.0 weight percent, and most preferably from about 0.3 weight percent to about 1.2 weight percent, based on the weight of the metallurgical powder composition.
- The metallurgical powder compositions of the present invention may also optionally contain alloying powders in addition to the carbon powder. The term “alloying powder” as used herein refers to any particulate element, compound, or alloy powder physically blended with the metallurgical powder composition, whether or not that additive ultimately alloys or partially alloys with the metallurgical powder composition.
- Examples of optional alloying powders that may be present in the metallurgical powder composition include elements, compounds, or alloys containing molybdenum, manganese, copper, nickel, chromium, silicon, gold, vanadium, columbium (niobium), phosphorus, aluminum, boron, or oxides thereof; binary alloys of copper and tin, copper and nickel, or copper and phosphorous; ferro-alloys of manganese, chromium, boron, phosphorus, or silicon; low melting ternary and quaternary eutectics of carbon in combination with elements selected from iron, vanadium, manganese, chromium, molybdenum or combinations thereof; carbides of tungsten or silicon; silicon nitride; aluminum oxide; and sulfides of manganese or molybdenum, and combinations thereof. Preferred alloying powders include elements, compounds, or alloys containing molybdenum, manganese, copper, nickel, chromium, vanadium, phosphorus, or combinations thereof, and more preferably elements, compounds, or alloys containing copper, nickel, or combinations thereof.
- The alloying powders are preferably present in the metallurgical powder composition in amounts of up to about 10 weight percent, and typically in the range of from about 0.25 to about 10 weight percent, preferably from about 0.25 to about 7 weight percent, and more preferably from about 0.5 to about 5 weight percent. The alloying powders generally have a weight average particle size below about 100 microns, preferably below about 75 microns, more preferably below about 30 microns, and most preferably in the range of about 5 microns to about 20 microns. The particle size of the alloying powders is generally relatively small and can be analyzed by laser light scattering technology as opposed to screening techniques. Laser light scattering technology reports the particle size distribution in dx values, where it is said that “x” percent by volume of the powder has a diameter below the reported value. The alloying particles generally have a particle size distribution such that they have a d90 value of below about 100 microns, preferably below about 75 microns, and more preferably below about 50 microns; and a d50 value of below about 75 microns, preferably below about 50 microns, and more preferably below about 30 microns.
- In a preferred embodiment of the present invention, the metallurgical powder composition contains an alloying powder containing copper. The copper provides hardenability properties to metal parts formed from the metallurgical powder compositions. The copper containing powder is preferably elemental copper having relatively few impurities. Preferably the copper containing powder contains at least 90 weight percent, more preferably at least 98 weight percent, and most preferably at least 99.5 weight percent copper based on the total weight of the copper containing powder.
- Preferably, the amount of copper containing powder present in the metallurgical powder composition of the present invention is such that there is at least 0.2 weight percent, more preferably from about from about 0.5 weight percent to about 4.0 weight percent, and most preferably from about 1.0 to about 3.0 weight percent elemental copper, based on the total weight of the metallurgical powder composition.
- The metallurgical powder compositions of the present invention may also include any special-purpose additive commonly used with metallurgical composition such as lubricants, machining agents, and plasticizers.
- In a preferred embodiment of the present invention the metallurgical powder composition contains a lubricant to reduce the ejection force required to remove a compacted part from the die cavity. Examples of typical powder metallurgy lubricants include the stearates, such as zinc stearate, lithium stearate, manganese stearate, or calcium stearate; synthetic waxes, such as ethylene bisstearamide or polyolefins; or combinations thereof. The lubricant may also be a polyamide lubricant, such as PROMOLD-450, disclosed in U.S. Pat. No. 5,368,630, particulate ethers disclosed in U.S. Pat. No. 5,498,276, to Luk, or a metal salt of a fatty acid disclosed in U.S. Pat. No. 5,330,792 to Johnson et al., the disclosures of which are hereby incorporated by reference in their entireties. The lubricant may also be a combination of any of the aforementioned lubricants described above.
- The lubricant is generally added in an amount of up to about 2.0 weight percent, preferably from about 0.1 to about 1.5 weight percent, more preferably from about 0.1 to about 1.0 weight percent, and most preferably from about 0.2 to about 0.75 weight percent, of the metallurgical powder composition.
- Preferred lubricants are ethylene bisstearamide, zinc stearate, Kenolube™ (supplied by Hoganas Corporation, located in Hoganas, Sweden), Ferrolube™ (supplied by Blanchford), and polyethylene wax. Preferably, these lubricants are added in an amount of from about 0.2 weight percent to about 1.5 weight percent based on the total weight of the metallurgical powder composition formed.
- Other additives may also be present in the metallurgical powder compositions, such as plasticizers and machining agents. Preferably, these other additives are present in the metallurgical powder composition in an amount of from about 0.05 weight percent to about 1.5 weight percent, and more preferably from about 0.1 weight percent to about 0.5 weight percent based on the total weight of the metallurgical powder composition. Plasticizers, such as polyethylene-polypropylene copolymer, are typically used in connection with binders and/or lubricants. Machining agents, such as molybdenum sulfides, iron sulfides, boron nitride, boric acid, or combinations thereof are typically used to aid in final machining operations. In a preferred embodiment, manganese sulfide is present in the metallurgical powder composition in an amount of from about 0.1 weight percent to about 0.75 weight percent based on the weight of the metallurgical powder composition.
- The metallurgical powder composition may also contain one or more binding agents to bond the different components present in the metallurgical powder compostion so as to inhibit segregation. By “bond” as used herein, it is meant any physical or chemical method that facilitates adhesion of the components of the metallurgical powder composition.
- In a preferred embodiment of the present invention, bonding is carried out through the use of at least one binding agent. Binding agents that can be used in the present invention are those commonly employed in the powder metallurgical arts. Examples of such binding agents are found in U.S. Pat. No. 4,834,800 to Semel, U.S. Pat. No. 4,483,905 to Engstrom, U.S. Pat. No. 5,154,881 to Rutz et al., and U.S. Pat. No. 5,298,055 to Semel et.al., the disclosures of which are hereby incorporated by reference in their entireties.
- Such binding agents include, for example, polyglycols such as polyethylene glycol or polypropylene glycol; glycerine; polyvinyl alcohol; homopolymers or copolymers of vinyl acetate; cellulosic ester or ether resins; methacrylate polymers or copolymers; alkyd resins; polyurethane resins; polyester resins; or combinations thereof. Other examples of binding agents that are useful are the relatively high molecular weight polyalkylene oxide-based compositions described in U.S. Pat. No. 5,298,055 to Semel et al. Useful binding agents also include the dibasic organic acid, such as azelaic acid, and one or more polar components such as polyethers (liquid or solid) and acrylic resins as disclosed in U.S. Pat. No. 5,290,336 to Luk, which is incorporated herein by reference in its entirety. The binding agents in the '336 Patent to Luk can also advantageously act as lubricants. Additional useful binding agents include the cellulose ester resins, hydroxy alkylcellulose resins, and thermoplastic phenolic resins described in U.S. Pat. No. 5,368,630 to Luk, which is incorporated herein by reference in its entirety.
- The binding agent can further be the low melting, solid polymers or waxes, e.g., a polymer or wax having a softening temperature of below 200° C. (390° F.), such as polyesters, polyethylenes, epoxies, urethanes, paraffins, ethylene bisstearamides, and cotton seed waxes, and also polyolefins with weight average molecular weights below 3,000, and hydrogenated vegetable oils that are C14-24 alkyl moiety triglycerides and derivatives thereof, including hydrogenated derivatives, e.g. cottonseed oil, soybean oil, jojoba oil, and blends thereof, as described in WO 99/20689, published Apr. 29, 1999, which is hereby incorporated by reference in its entirety herein. These binding agents can be applied by the dry bonding techniques discussed in that application and in the general amounts set forth above for binding agents. Further binding agents that can be used in the present invention are polyvinyl pyrrolidone as disclosed in U.S. Pat. No. 5,069,714, which is incorporated herein in its entirety by reference, or tall oil esters. Preferred binding agents are polyethylene oxide and polyvinylacetate, or combinations thereof, which are binding agents disclosed in WO 99/20689,
- The amount of binding agent present in the metallurgical powder composition depends on such factors as the density, particle size distribution and amounts of the iron-alloy powder, the iron powder and optional alloying powder in the metallurgical powder composition. Generally, the binding agent will be added in an amount of at least about 0.005 weight percent, more preferably from about 0.005 weight percent to about 2 weight percent, and most preferably from about 0.05 weight percent to about 1 weight percent, based on the total weight of the metallurgical powder composition.
- In a preferred embodiment of the present invention, the metallurgical powder composition contains from about 10 weight percent to about 20 weight percent of an iron-molybdenum prealloy powder, from about 80 weight percent to about 90 weight percent substantially pure iron powder, from about 0.1 weight percent to about 1.2 weight percent carbon that is preferably graphite powder, and from about 0.1 to about 3.0 weight percent of copper that is preferably in the form of a copper containing powder. In this embodiment, the iron-molybdenum prealloy powder preferably contains from about 0.4 weight percent to about 2.0 weight percent molybdenum and from about 98 weight percent to about 99.6 weight percent iron. The percentages of iron, molybdenum, carbon and copper in the metallurgical powder composition can be determined for example by an elemental analysis.
- The present invention also provides methods of preparing metallurgical powder compositions. In the methods of the present invention, an iron-alloy powder that has preferably been prepared in accordance with the methods as previously described herein is provided. The iron-alloy powder is admixed with substantially pure iron powder and preferably carbon powder, in the amounts previously described herein, to form the metallurgical powder compositions of the present invention. Additionally other additives can be added to the metallurgical powder composition in the amounts previously described herein. For example, any combination of alloying powders, lubricants, binding agents, machining agents, plasticizers, or any other conventional metallurgical powder additive may be added.
- The method of combining the iron-alloy powder, the substantially pure iron powder, the carbon powder, and other desired additives may be performed according to any technique well known to those skilled in the art. Preferably, the method used results in a uniformly mixed metallurgical powder composition that does not readily segregate. Moreover, the order of addition of the iron-alloy powder, the substantially pure iron powder, the carbon powder, and other desired additives is not critical. Preferably, however the order of addition is in a manner to achieve a uniform mixture of the metallurgical powder composition.
- In a preferred embodiment, the methods of the present invention include adding a binding agent to the metallurgical powder composition to bond the iron-alloy powder, the substantially pure iron powder and other additives to inhibit segregation. The binding agent can be added to the powder mixture according to any technique known to those skilled in the art. For example, the procedures taught by U.S. Pat. Nos. 4,834,800 to Semel; 4,483,905 to Engstrom; 5,154,881 to Rutz et al.; and 5,298,055 to Semel et al.; and WO 99/20689, published Apr. 29, 1999, can be used, the disclosures of which are hereby incorporated by reference in their entireties. Preferably, the binding agent is added in a liquid form and mixed with the powders until good wetting of the powders is attained. Those binding agents that are in liquid form at ambient conditions can be added to the powder as such, but it is preferred that the binding agent, whether liquid or solid, be dissolved or dispersed in an organic solvent and added as a liquid solution, thereby providing substantially homogeneous distribution of the binding agent throughout the mixture. The wet powder is thereafter processed using conventional techniques to remove the solvent. Typically, if the mixes are small, generally 5 lbs. or less, the wet powder is spread over a shallow tray and allowed to dry in air. On the other hand, in the case of larger mixes, the drying step can be accomplished in the mixing vessel by employing heat and vacuum.
- Also, the sequence of addition of the binding agent and a lubricant, if desired, can be varied to alter the final characteristics of the metallurgical powder composition. For example, the procedures taught in U.S. Pat. No. 5,256,185 to Semel et al., which is hereby incorporated by reference in its entirety, can be used. Also for example, the lubricant can be blended with the iron-alloy powder, the substantially pure iron powder, the carbon powder, the alloying powders and other optional additives, and then, subsequently, the binding agent is applied to that composition. In another method, a portion of the lubricant, preferably from about 50 to about 99 weight percent, more preferably from about 75 to about 95 weight percent, is added to a mixture of the iron-alloy powder, the substantially pure iron powder, and other additives, then the binding agent is added, followed by removal of the solvent, and subsequently the rest of the lubricant is added to the metal powder composition. One further method is to add the binding agent first to a mixture of the iron-alloy powder and other additives, remove the solvent, and subsequently add the entire amount of the lubricant.
- The metallurgical powder compositions of the present invention thus formed can be compacted in a die according to standard metallurgical techniques to form metal parts. Typical compaction pressures range between about 5 and 200 tons per square inch (tsi) (69-2760 MPa), preferably from about 20-100 tsi (276-1379 MPa), and more preferably from about 25-60 tsi (345-828 MPa).
- Following compaction, the part can be sintered, according to standard metallurgical techniques at temperatures, sintering times, and other conditions appropriate to the metallurgical powder composition. For example, in a preferred embodiment, sintering temperatures range from about 1900° F. to about 2400° F. and are conducted for a time sufficient to achieve metallurgical bonding and alloying. The metallurgical powder composition may also be double pressed and double sintered by techniques well known to those skilled in the art.
- Metal parts of various shapes and for various uses may be formed from the metallurgical powder compositions of the present invention. For example, the metal parts may be shaped for use in the automotive, aerospace, or nuclear energy industries.
- It has been found that the metallurgical powder compositions made in accordance with the methods of the present invention have unexpectedly superior machinability properties. These improvements are especially observed when the metallurgical powder composition contains from about 10 weight percent to about 30 weight percent of an iron-molybdenum prealloy powder, from about 70 weight percent to about 90 weight percent of a substantially pure iron powder, from about 0.1 weight percent to about 3.0 weight percent of a carbon powder, and from about 0.1 weight percent to about 3.0 weight percent of a copper containing powder. Preferably, the iron molybdenum prealloy contains from about 0.40 to about 2.0 weight percent molybdenum and from about 98 weight percent to about 99.6 weight percent iron. The machinability can be further enhanced through the presence of a machining agent such as manganese sulfide in the metallurgical powder composition.
- Some embodiments of the present invention will now be described in detail in the following Examples. Iron-based metallurgical powder compositions were prepared in accordance with the methods of the present invention. Comparative metal powder compositions were also prepared. The powder compositions prepared were compacted and sintered to form metal parts and evaluated for machinability.
- Metallurgical powder compositions having the compositions shown in Table 1 were prepared.
TABLE 1 Composition of Metal Powders Tested Fe Fe-Alloy Carbon Cu MnS Lubricant Examples Powder Powder, wt % wt % wt % wt % wt % Control Balance 0.0 0.5 2.0 0.0 0.0 Comp. Ex. Balance 0.0 0.6 1.75 0.0 0.75 1 Comp. Ex. Balance 0.0 0.6 1.75 0.35 0.75 2 Example 3 Balance 10.0 0.6 2.0 0.35 0.75 Example 4 Balance 15.0 0.6 2.0 0.35 0.75 Example 5 Balance 20.0 0.6 1.75 0.35 0.75 Example 6 Balance 20.0 0.6 2.0 0.35 0.75 Example 7 Balance 25.0 0.6 2.0 0.35 0.75 Example 8 Balance 30.0 0.6 2.0 0.35 0.75 Example 9 Balance 35.0 0.6 2.0 0.35 0.75 Example Balance 40.0 0.6 2.0 0.35 0.75 10 - The compositions were prepared by uniformly blending all the ingredients in the amounts shown in Table 1. The iron powder used in all examples was Ancorsteel 1000A available from Hoeganaes Corporation, located in Cinnaminson, N.J. The iron-alloy powder used in all examples was Ancorsteel™ 85HP steel powder also available from Hoeganaes Corporation. Ancorsteel 85HP is an iron-molybdenum prealloy powder containing about 0.85 weight percent molybdenum. The graphite used in all examples (shown as “Carbon” in Table 1) had a weight average particle size of about 6 to 8 microns and was obtained from Asbury Graphite Mills, Inc., located in Asbury, N.J. The copper powder (shown as “Cu” in Table 1) used in all examples was Accupowder from Accupowder Corporation. The copper powder had a weight average particle size of from about 10 microns to about 14 microns and a purity of 99.5 weight percent. The “MnS” shown in Table 1 is manganese sulfide, a machining agent. The lubricant shown in Table 1 was Acrawax™ C lubricant. Acrawax C is a synthetic wax and was obtained from Algroup Lonza located in Fair Lawn, N.J.
- The metal powder compositions of Comparative Examples 1 to 2 and Examples 3 to 10 were evaluated for machinability.
- To evaluate machinability, each of the metallurgical powder compositions in Table 1 were compacted into 4 inch diameter by 1 inch thick discs having a density of 6.8 g/cm3. The discs were sintered at 2050° F. for 30 minutes in an atmosphere of 10% hydrogen and 90% nitrogen and allowed to cool to ambient temperature.
- Prior to conducting the machinability tests, each drill bit was calibrated in the following manner. Twenty drill bits of 0.25 inch diameter were used to drill 0.95 inch deep holes in discs formed from the “Control” powder shown in Table 1. Each drill bit was used to drill approximately 2 to 3 holes for a total of about 40 to about 60 holes. The holes were drilled at a feed rate of 0.005 inches per revolution and a cutting speed of 2220 rpm. During drilling the drill torque and drill thrust were measured automatically for each drill bit, and an average drill torque and thrust were calculated from all measurements. Only drill bits having a drill torque and thrust within ±5 percent of the average were used in the machinability tests.
- Using the same equipment used to calibrate the drill bits, discs formed from each of the metallurgical powder compositions shown in Table 1 were drilled with holes having a depth of 0.95 inches until the drill bit failed (e.g., wear exceeds a predetermined level). For each hole drilled, a feed rate of 0.005 inches per revolution and a cutting speed of 2220 rpm was used. The drill torque and drill thrust were measured throughout the test, and wear measurements on the drill bit were taken every ten holes drilled. The wear measurements were taken by a Microdynascope Model 5E Universal Inspection and Gauging System, supplied by Vision Engineering, located in Surrey, England. Table 2 shows the results of the machinability testing. The mean thrust was the mean value of thrust for all holes drilled prior to failure of the drill bit. Table 2 also shows the number of holes drilled to failure that was used for calculating the mean thrust. The number of holes drilled to failure depended in part on the strength of the material (increasing the strength decreases the number of holes to failure).
TABLE 2 Machinability Results Composition Wt % of Number of Holes Mean Thrust, of Disc Prelloy Powder Drilled to Failure (lbs) Comp. Ex. 1 0.0 95 273.0 Comp. Ex. 2 0.0 775 210.6 Example 3 10.0 34 161.6 Example 4 15.0 622 166.0 Example 5 20.0 838 167.2 Example 6 20.0 398 195.5 Example 7 25.0 550 223.3 Example 8 30.0 383 140.7 Example 9 35.0 435 129.5 Example 10 40.0 476 131.0 - The results in Table 2 show that the addition of the iron-alloy powder in an metallurgical powder composition reduces the mean thrust of a drill bit during the drilling of a disc. For example, although the mean thrust can be reduced somewhat by the addition of manganese sulfide to an iron based powder composition (see comparative Example 1 in comparison to Comparative Example 2), further improvement can be achieved by addition of a iron-alloy powder. The results for mean thrust obtained for Comparative Examples 1 to 2 and Example 5 are shown in FIG. 1. FIG. 1 is a bar graph showing mean thrust for discs prepared from Comparative Examples 1 to 2 and Example 5. By reducing the mean thrust, there is less wear on the drill bit leading to such benefits as increased lifetime of the drill bit.
- There have thus been described certain preferred embodiments of the improved metallurgical powder compositions of the present invention, and methods of making and using the same. While preferred embodiments have been disclosed and described, it will be recognized by those with skill in the art that variations and modifications are within the true spirit and scope of the invention. The appended claims are intended to cover all such variations and modifications.
Claims (16)
1. A method of making a metallurgical powder composition comprising the steps of:
(a) providing an iron-alloy powder comprising iron and at least one alloying additive, wherein the alloying additive is present in an amount of from about 0.01 weight percent to about 7 weight percent and the iron is present in an amount of at least 85 weight percent based on the total weight of the iron-alloy powder; and
(b) admixing with the iron-alloy powder a substantially pure iron powder and carbon to form a metallurgical powder composition, wherein the metallurgical powder composition comprises from about 5 weight percent to about 40 weight percent of the iron-alloy powder, at least 55 percent by weight of the substantially pure iron powder, and at least 0.1 weight percent of the carbon based on the total weight of the metallurgical powder composition.
2. The method of claim 1 wherein the alloying additive in the iron-alloy powder is selected from the group consisting of molybdenum, chromium, vanadium, tungsten, and combinations thereof.
3. The method of claim 2 wherein the alloying additive is molybdenum.
4. The method of claim 3 wherein the molybdenum is present in the iron-alloy powder in an amount of from about 0.1 to about 2.0 weight percent, based on the total weight of the iron-alloy powder.
5. The method of claim 1 wherein the metallurgical powder composition further comprises at least one alloying powder.
6. The method of claim 5 wherein the alloying powder comprises copper, nickel, or combinations thereof.
7. The method of claim 1 wherein the metallurgical powder composition further comprises copper, nickel, graphite, manganese sulfide, or combinations thereof.
8. The method of claim 1 wherein the metallurgical powder composition comprises from about 10 weight percent to about 30 weight percent of the iron-alloy powder based on the total weight of the metallurgical powder composition and wherein the iron-alloy powder comprises from about 0.1 weight percent to about 2 weight percent molybdenum based on the total weight of the iron-alloy powder.
9. The method of claim 8 wherein the metallurgical powder composition comprises from about 70 weight percent to about 95 weight percent of the substantially pure iron powder, from about 0.1 weight percent to about 3 weight percent carbon, and from about 0.10 to about 3.0 weight percent copper, based on the total weight of the metallurgical powder composition.
10. An improved metallurgical powder composition comprising:
(a) from about 5 weight percent to about 40 weight percent of an iron-molybdenum alloy powder comprising iron and molybdenum, wherein the amount of molybdenum is from about 0.10 weight percent to about 7.0 weight percent and the amount of iron is at least 85 weight percent based on the weight of the iron-molybdenum alloy powder;
(b) at least 55 weight percent of a substantially pure iron powder; and
(c) from about 0.1 weight percent to about 3 weight percent of carbon.
11. The metallurgical powder composition of claim 10 wherein the metallurgical composition further comprises at least one alloying powder.
12. The metallurgical powder composition of claim 10 wherein the metallurgical composition further comprises nickel, copper, graphite, manganese sulfide, or combinations thereof.
13. The metallurgical powder composition of claim 10 wherein the metallurgical powder composition comprises from about 10 weight percent to about 30 weight percent of the iron-molybdenum alloy powder, from about 70 weight percent to about 95 weight percent of the substantially pure iron, from about 0.1 weight percent to about 2 weight percent of the carbon, and from about 0.10 to about 3.0 weight percent copper, based on the total weight of the metallurgical powder composition.
14. A method of forming a metal part comprising the steps of:
(a) providing a metallurgical powder composition comprising a mixture of:
(i) from about 5 weight percent to about 40 weight percent, based on the weight of the metallurgical powder composition, of a iron-alloy powder comprising iron and at least one alloying additive, wherein the alloying additive is present in an amount of from about 0.01 weight percent to about 7 weight percent and the iron is present in an amount of at least 85 weight percent, based on the total weight of the iron-alloy powder;
(ii) at least 55 weight percent of substantially pure iron powder; and
(iii) at least about 0.1 weight percent of carbon; and
(b) compacting the metallurgical powder composition at a pressure of at least about 5 tsi to form a metal part.
15. The method of claim 14 wherein the alloying additive is molybdenum and is present in the iron-alloy powder in an amount of from about 0.1 to about 3.0 weight percent, based on the total weight of the iron-alloy powder.
16. The method of claim 15 further comprising the step of sintering the compacted metal part at a temperature of at least 1900° F. to form a machinable metal sintered part.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/266,316 US20030103858A1 (en) | 1999-11-04 | 2002-10-08 | Metallurgical powder compositions and methods of making and using the same |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US43400099A | 1999-11-04 | 1999-11-04 | |
US10/266,316 US20030103858A1 (en) | 1999-11-04 | 2002-10-08 | Metallurgical powder compositions and methods of making and using the same |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US43400099A Continuation | 1999-11-04 | 1999-11-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
US20030103858A1 true US20030103858A1 (en) | 2003-06-05 |
Family
ID=23722409
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/266,316 Abandoned US20030103858A1 (en) | 1999-11-04 | 2002-10-08 | Metallurgical powder compositions and methods of making and using the same |
Country Status (9)
Country | Link |
---|---|
US (1) | US20030103858A1 (en) |
EP (1) | EP1246949B1 (en) |
JP (1) | JP2003514112A (en) |
KR (1) | KR100697534B1 (en) |
AT (1) | ATE317458T1 (en) |
AU (1) | AU7758000A (en) |
DE (1) | DE60025931T2 (en) |
MX (1) | MXPA02004478A (en) |
WO (1) | WO2001032946A1 (en) |
Cited By (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030003009A1 (en) * | 2001-06-13 | 2003-01-02 | Kabushiki Kaisha Toyota Chuo Kenkyusho | Pressurizing forming process and presurized-and-formed member |
US20040123697A1 (en) * | 2002-10-22 | 2004-07-01 | Mikhail Kejzelman | Method of preparing iron-based components |
US20040206204A1 (en) * | 2001-05-18 | 2004-10-21 | Hoganas Ab | Metal powder including diffusion alloyed molybdenum |
US20060222554A1 (en) * | 2005-04-04 | 2006-10-05 | Tajpreet Singh | Diffusion bonded nickel-copper powder metallurgy powder |
EP2101940A1 (en) * | 2006-12-29 | 2009-09-23 | Höganäs Ab (publ) | Powder, method of manufacturing a component and component |
US20170029929A1 (en) * | 2014-05-31 | 2017-02-02 | Element Six Gmbh | Method of coating a body, granules for the method and method of making granules |
US20170113272A1 (en) * | 2012-02-24 | 2017-04-27 | Hoeganaes Corporation | Lubricant System For Use In Powder Metallurgy |
WO2019046324A1 (en) * | 2017-08-28 | 2019-03-07 | Monolith Materials, Inc. | Particle systems and methods |
US10370539B2 (en) | 2014-01-30 | 2019-08-06 | Monolith Materials, Inc. | System for high temperature chemical processing |
US10618026B2 (en) | 2015-02-03 | 2020-04-14 | Monolith Materials, Inc. | Regenerative cooling method and apparatus |
US10808097B2 (en) | 2015-09-14 | 2020-10-20 | Monolith Materials, Inc. | Carbon black from natural gas |
US11149148B2 (en) | 2016-04-29 | 2021-10-19 | Monolith Materials, Inc. | Secondary heat addition to particle production process and apparatus |
US11203692B2 (en) | 2014-01-30 | 2021-12-21 | Monolith Materials, Inc. | Plasma gas throat assembly and method |
US11304288B2 (en) | 2014-01-31 | 2022-04-12 | Monolith Materials, Inc. | Plasma torch design |
US11453784B2 (en) | 2017-10-24 | 2022-09-27 | Monolith Materials, Inc. | Carbon particles having specific contents of polycylic aromatic hydrocarbon and benzo[a]pyrene |
US11492496B2 (en) | 2016-04-29 | 2022-11-08 | Monolith Materials, Inc. | Torch stinger method and apparatus |
US11665808B2 (en) | 2015-07-29 | 2023-05-30 | Monolith Materials, Inc. | DC plasma torch electrical power design method and apparatus |
US11760884B2 (en) | 2017-04-20 | 2023-09-19 | Monolith Materials, Inc. | Carbon particles having high purities and methods for making same |
US11926743B2 (en) | 2017-03-08 | 2024-03-12 | Monolith Materials, Inc. | Systems and methods of making carbon particles with thermal transfer gas |
US11939477B2 (en) | 2014-01-30 | 2024-03-26 | Monolith Materials, Inc. | High temperature heat integration method of making carbon black |
US11987712B2 (en) | 2015-02-03 | 2024-05-21 | Monolith Materials, Inc. | Carbon black generating system |
US12030776B2 (en) | 2017-08-28 | 2024-07-09 | Monolith Materials, Inc. | Systems and methods for particle generation |
US12119133B2 (en) | 2015-09-09 | 2024-10-15 | Monolith Materials, Inc. | Circular few layer graphene |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE0101776D0 (en) * | 2001-05-18 | 2001-05-18 | Hoeganaes Ab | Metal powder |
KR100437643B1 (en) * | 2001-11-30 | 2004-06-30 | 가야에이엠에이 주식회사 | compositions of manganese sulfide compound an addition for making sintered goods |
KR101076353B1 (en) | 2006-08-28 | 2011-10-25 | 파나소닉 전공 주식회사 | Metal powder for metal-laser sintering and metal-laser sintering process using the same |
WO2011146454A1 (en) * | 2010-05-19 | 2011-11-24 | Hoeganaes Corporation | Compositions and methods for improved dimensional control in ferrous poweder metallurgy applications |
KR101531347B1 (en) * | 2012-12-24 | 2015-06-25 | 주식회사 포스코 | Method for manufacturing iron-based diffusion bonding powders |
KR102312281B1 (en) * | 2021-04-26 | 2021-10-12 | 대영소결금속 주식회사 | Manganese sulfide composition for sintering material manufacturing |
Citations (42)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4018632A (en) * | 1976-03-12 | 1977-04-19 | Chrysler Corporation | Machinable powder metal parts |
US4166736A (en) * | 1978-06-14 | 1979-09-04 | Metallurgical International, Inc. | Powdered metal filter composition and processes for producing the same |
US4287068A (en) * | 1978-06-14 | 1981-09-01 | Metallurgical International, Inc. | Powdered metal filter composition and processes for producing the same |
US4382818A (en) * | 1975-12-08 | 1983-05-10 | Ford Motor Company | Method of making sintered powder alloy compacts |
US4483905A (en) * | 1980-03-06 | 1984-11-20 | Hoganas Ag | Homogeneous iron based powder mixtures free of segregation |
US4676831A (en) * | 1983-09-09 | 1987-06-30 | Hoganas Ab | Powder mixture containing talloil free of segregation |
US4834800A (en) * | 1986-10-15 | 1989-05-30 | Hoeganaes Corporation | Iron-based powder mixtures |
US4927461A (en) * | 1988-11-02 | 1990-05-22 | Quebec Metal Powders, Ltd. | Machinable-grade, ferrous powder blend containing boron nitride and method thereof |
US4975333A (en) * | 1989-03-15 | 1990-12-04 | Hoeganaes Corporation | Metal coatings on metal powders |
US5063011A (en) * | 1989-06-12 | 1991-11-05 | Hoeganaes Corporation | Doubly-coated iron particles |
US5069714A (en) * | 1990-01-17 | 1991-12-03 | Quebec Metal Powders Limited | Segregation-free metallurgical powder blends using polyvinyl pyrrolidone binder |
US5080712A (en) * | 1990-05-16 | 1992-01-14 | Hoeganaes Corporation | Optimized double press-double sinter powder metallurgy method |
US5108493A (en) * | 1991-05-03 | 1992-04-28 | Hoeganaes Corporation | Steel powder admixture having distinct prealloyed powder of iron alloys |
US5135566A (en) * | 1987-09-30 | 1992-08-04 | Kawasaki Steel Corporation | Iron base powder mixture and method |
US5154881A (en) * | 1992-02-14 | 1992-10-13 | Hoeganaes Corporation | Method of making a sintered metal component |
US5217683A (en) * | 1991-05-03 | 1993-06-08 | Hoeganaes Corporation | Steel powder composition |
US5225459A (en) * | 1992-01-31 | 1993-07-06 | Hoeganaes Corporation | Method of making an iron/polymer powder composition |
US5240742A (en) * | 1991-03-25 | 1993-08-31 | Hoeganaes Corporation | Method of producing metal coatings on metal powders |
US5256185A (en) * | 1992-07-17 | 1993-10-26 | Hoeganaes Corporation | Method for preparing binder-treated metallurgical powders containing an organic lubricant |
US5279640A (en) * | 1992-09-22 | 1994-01-18 | Kawasaki Steel Corporation | Method of making iron-based powder mixture |
US5290336A (en) * | 1992-05-04 | 1994-03-01 | Hoeganaes Corporation | Iron-based powder compositions containing novel binder/lubricants |
US5298055A (en) * | 1992-03-09 | 1994-03-29 | Hoeganaes Corporation | Iron-based powder mixtures containing binder-lubricant |
US5330792A (en) * | 1992-11-13 | 1994-07-19 | Hoeganaes Corporation | Method of making lubricated metallurgical powder composition |
US5368630A (en) * | 1993-04-13 | 1994-11-29 | Hoeganaes Corporation | Metal powder compositions containing binding agents for elevated temperature compaction |
US5397530A (en) * | 1993-04-26 | 1995-03-14 | Hoeganaes Corporation | Methods and apparatus for heating metal powders |
US5476374A (en) * | 1994-12-01 | 1995-12-19 | Langreck; Gerald K. | Axially ported variable volume gerotor pump technology |
US5498276A (en) * | 1994-09-14 | 1996-03-12 | Hoeganaes Corporation | Iron-based powder compositions containing green strengh enhancing lubricants |
US5518639A (en) * | 1994-08-12 | 1996-05-21 | Hoeganaes Corp. | Powder metallurgy lubricant composition and methods for using same |
US5534220A (en) * | 1992-04-01 | 1996-07-09 | Brico Engineering Limited | Method of sintering machinable ferrous-based materials |
US5543174A (en) * | 1989-06-12 | 1996-08-06 | Hoeganaes Corporation | Thermoplastic coated magnetic powder compositions and methods of making same |
US5599377A (en) * | 1994-07-28 | 1997-02-04 | Kawasaki Steel Corporation | Mixed iron powder for powder metallurgy |
US5613180A (en) * | 1994-09-30 | 1997-03-18 | Keystone Investment Corporation | High density ferrous power metal alloy |
US5637132A (en) * | 1990-03-06 | 1997-06-10 | United States Bronze Powders, Inc. | Powder metallurgy compositions |
US5656787A (en) * | 1994-02-08 | 1997-08-12 | Stackpole Limited | Hi-density sintered alloy |
US5679909A (en) * | 1995-03-24 | 1997-10-21 | Toyota Jidosha Kabushiki Kaisha | Sintered material having good machinability and process for producing the same |
US5766304A (en) * | 1995-04-25 | 1998-06-16 | Kawasaki Steel Corporation | Iron-base powder mixture for powder metallurgy and manufacturing method therefor |
US5782954A (en) * | 1995-06-07 | 1998-07-21 | Hoeganaes Corporation | Iron-based metallurgical compositions containing flow agents and methods for using same |
US5803037A (en) * | 1996-06-07 | 1998-09-08 | Nippon Piston Ring Co., Ltd. | Joined type valve seat |
US5872322A (en) * | 1997-02-03 | 1999-02-16 | Ford Global Technologies, Inc. | Liquid phase sintered powder metal articles |
US5881354A (en) * | 1996-05-03 | 1999-03-09 | Stackpole Limited | Sintered hi-density process with forming |
US6068813A (en) * | 1999-05-26 | 2000-05-30 | Hoeganaes Corporation | Method of making powder metallurgical compositions |
US6346133B1 (en) * | 1999-09-03 | 2002-02-12 | Hoeganaes Corporation | Metal-based powder compositions containing silicon carbide as an alloying powder |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02294066A (en) * | 1989-05-08 | 1990-12-05 | Mitsubishi Electric Corp | Read only memory |
US5997805A (en) * | 1997-06-19 | 1999-12-07 | Stackpole Limited | High carbon, high density forming |
-
2000
- 2000-08-08 MX MXPA02004478A patent/MXPA02004478A/en unknown
- 2000-08-08 AU AU77580/00A patent/AU7758000A/en not_active Abandoned
- 2000-08-08 JP JP2001535624A patent/JP2003514112A/en active Pending
- 2000-08-08 DE DE60025931T patent/DE60025931T2/en not_active Expired - Fee Related
- 2000-08-08 EP EP00967370A patent/EP1246949B1/en not_active Expired - Lifetime
- 2000-08-08 KR KR1020027005626A patent/KR100697534B1/en not_active IP Right Cessation
- 2000-08-08 WO PCT/US2000/040594 patent/WO2001032946A1/en active IP Right Grant
- 2000-08-08 AT AT00967370T patent/ATE317458T1/en not_active IP Right Cessation
-
2002
- 2002-10-08 US US10/266,316 patent/US20030103858A1/en not_active Abandoned
Patent Citations (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4382818A (en) * | 1975-12-08 | 1983-05-10 | Ford Motor Company | Method of making sintered powder alloy compacts |
US4018632A (en) * | 1976-03-12 | 1977-04-19 | Chrysler Corporation | Machinable powder metal parts |
US4166736A (en) * | 1978-06-14 | 1979-09-04 | Metallurgical International, Inc. | Powdered metal filter composition and processes for producing the same |
US4287068A (en) * | 1978-06-14 | 1981-09-01 | Metallurgical International, Inc. | Powdered metal filter composition and processes for producing the same |
US4483905A (en) * | 1980-03-06 | 1984-11-20 | Hoganas Ag | Homogeneous iron based powder mixtures free of segregation |
US4483905B1 (en) * | 1980-03-06 | 1997-02-04 | Hoeganaes Ab | Homogeneous iron based powder mixtures free of segregation |
US4676831A (en) * | 1983-09-09 | 1987-06-30 | Hoganas Ab | Powder mixture containing talloil free of segregation |
US4834800A (en) * | 1986-10-15 | 1989-05-30 | Hoeganaes Corporation | Iron-based powder mixtures |
US5135566A (en) * | 1987-09-30 | 1992-08-04 | Kawasaki Steel Corporation | Iron base powder mixture and method |
US4927461A (en) * | 1988-11-02 | 1990-05-22 | Quebec Metal Powders, Ltd. | Machinable-grade, ferrous powder blend containing boron nitride and method thereof |
US4975333A (en) * | 1989-03-15 | 1990-12-04 | Hoeganaes Corporation | Metal coatings on metal powders |
US5063011A (en) * | 1989-06-12 | 1991-11-05 | Hoeganaes Corporation | Doubly-coated iron particles |
US5543174A (en) * | 1989-06-12 | 1996-08-06 | Hoeganaes Corporation | Thermoplastic coated magnetic powder compositions and methods of making same |
US5069714A (en) * | 1990-01-17 | 1991-12-03 | Quebec Metal Powders Limited | Segregation-free metallurgical powder blends using polyvinyl pyrrolidone binder |
US5637132A (en) * | 1990-03-06 | 1997-06-10 | United States Bronze Powders, Inc. | Powder metallurgy compositions |
US5080712A (en) * | 1990-05-16 | 1992-01-14 | Hoeganaes Corporation | Optimized double press-double sinter powder metallurgy method |
US5080712B1 (en) * | 1990-05-16 | 1996-10-29 | Hoeganaes Corp | Optimized double press-double sinter powder metallurgy method |
US5240742A (en) * | 1991-03-25 | 1993-08-31 | Hoeganaes Corporation | Method of producing metal coatings on metal powders |
US5108493A (en) * | 1991-05-03 | 1992-04-28 | Hoeganaes Corporation | Steel powder admixture having distinct prealloyed powder of iron alloys |
US5217683A (en) * | 1991-05-03 | 1993-06-08 | Hoeganaes Corporation | Steel powder composition |
US5321060A (en) * | 1992-01-31 | 1994-06-14 | Hoeganaes Corporation | Method of making an iron/polymer powder composition |
US5225459A (en) * | 1992-01-31 | 1993-07-06 | Hoeganaes Corporation | Method of making an iron/polymer powder composition |
US5154881A (en) * | 1992-02-14 | 1992-10-13 | Hoeganaes Corporation | Method of making a sintered metal component |
US5484469A (en) * | 1992-02-14 | 1996-01-16 | Hoeganaes Corporation | Method of making a sintered metal component and metal powder compositions therefor |
US5298055A (en) * | 1992-03-09 | 1994-03-29 | Hoeganaes Corporation | Iron-based powder mixtures containing binder-lubricant |
US5534220A (en) * | 1992-04-01 | 1996-07-09 | Brico Engineering Limited | Method of sintering machinable ferrous-based materials |
US5290336A (en) * | 1992-05-04 | 1994-03-01 | Hoeganaes Corporation | Iron-based powder compositions containing novel binder/lubricants |
US5256185A (en) * | 1992-07-17 | 1993-10-26 | Hoeganaes Corporation | Method for preparing binder-treated metallurgical powders containing an organic lubricant |
US5279640A (en) * | 1992-09-22 | 1994-01-18 | Kawasaki Steel Corporation | Method of making iron-based powder mixture |
US5330792A (en) * | 1992-11-13 | 1994-07-19 | Hoeganaes Corporation | Method of making lubricated metallurgical powder composition |
US5429792A (en) * | 1993-04-13 | 1995-07-04 | Hoeganaes Corporation | Metal powder compositions containing binding agents for elevated temperature compaction |
US5368630A (en) * | 1993-04-13 | 1994-11-29 | Hoeganaes Corporation | Metal powder compositions containing binding agents for elevated temperature compaction |
US5397530A (en) * | 1993-04-26 | 1995-03-14 | Hoeganaes Corporation | Methods and apparatus for heating metal powders |
US5656787A (en) * | 1994-02-08 | 1997-08-12 | Stackpole Limited | Hi-density sintered alloy |
US5599377A (en) * | 1994-07-28 | 1997-02-04 | Kawasaki Steel Corporation | Mixed iron powder for powder metallurgy |
US5518639A (en) * | 1994-08-12 | 1996-05-21 | Hoeganaes Corp. | Powder metallurgy lubricant composition and methods for using same |
US5538684A (en) * | 1994-08-12 | 1996-07-23 | Hoeganaes Corporation | Powder metallurgy lubricant composition and methods for using same |
US5624631A (en) * | 1994-09-14 | 1997-04-29 | Hoeganaes Corporation | Iron-based powder compositions containing green strength enhancing lubricants |
US5498276A (en) * | 1994-09-14 | 1996-03-12 | Hoeganaes Corporation | Iron-based powder compositions containing green strengh enhancing lubricants |
US5613180A (en) * | 1994-09-30 | 1997-03-18 | Keystone Investment Corporation | High density ferrous power metal alloy |
US5476374A (en) * | 1994-12-01 | 1995-12-19 | Langreck; Gerald K. | Axially ported variable volume gerotor pump technology |
US5679909A (en) * | 1995-03-24 | 1997-10-21 | Toyota Jidosha Kabushiki Kaisha | Sintered material having good machinability and process for producing the same |
US5766304A (en) * | 1995-04-25 | 1998-06-16 | Kawasaki Steel Corporation | Iron-base powder mixture for powder metallurgy and manufacturing method therefor |
US5782954A (en) * | 1995-06-07 | 1998-07-21 | Hoeganaes Corporation | Iron-based metallurgical compositions containing flow agents and methods for using same |
US5881354A (en) * | 1996-05-03 | 1999-03-09 | Stackpole Limited | Sintered hi-density process with forming |
US5803037A (en) * | 1996-06-07 | 1998-09-08 | Nippon Piston Ring Co., Ltd. | Joined type valve seat |
US5872322A (en) * | 1997-02-03 | 1999-02-16 | Ford Global Technologies, Inc. | Liquid phase sintered powder metal articles |
US6068813A (en) * | 1999-05-26 | 2000-05-30 | Hoeganaes Corporation | Method of making powder metallurgical compositions |
US6346133B1 (en) * | 1999-09-03 | 2002-02-12 | Hoeganaes Corporation | Metal-based powder compositions containing silicon carbide as an alloying powder |
Cited By (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20040206204A1 (en) * | 2001-05-18 | 2004-10-21 | Hoganas Ab | Metal powder including diffusion alloyed molybdenum |
US20030003009A1 (en) * | 2001-06-13 | 2003-01-02 | Kabushiki Kaisha Toyota Chuo Kenkyusho | Pressurizing forming process and presurized-and-formed member |
US7459032B2 (en) * | 2001-06-13 | 2008-12-02 | Kabushiki Kaisha Toyota Chuo Kenkyusho | Pressurizing forming process and pressurized-and-formed member |
US20040123697A1 (en) * | 2002-10-22 | 2004-07-01 | Mikhail Kejzelman | Method of preparing iron-based components |
US7585459B2 (en) * | 2002-10-22 | 2009-09-08 | Höganäs Ab | Method of preparing iron-based components |
US20060222554A1 (en) * | 2005-04-04 | 2006-10-05 | Tajpreet Singh | Diffusion bonded nickel-copper powder metallurgy powder |
US7309374B2 (en) * | 2005-04-04 | 2007-12-18 | Inco Limited | Diffusion bonded nickel-copper powder metallurgy powder |
US8911662B2 (en) * | 2006-12-29 | 2014-12-16 | Hoganas Ab | Powder, method of manufacturing a component and component |
EP2101940A4 (en) * | 2006-12-29 | 2014-06-18 | Hoeganaes Ab Publ | Powder, method of manufacturing a component and component |
US20100054982A1 (en) * | 2006-12-29 | 2010-03-04 | Hoganas Ab | Powder, method of manufacturing a component and component |
EP2101940A1 (en) * | 2006-12-29 | 2009-09-23 | Höganäs Ab (publ) | Powder, method of manufacturing a component and component |
US20170113272A1 (en) * | 2012-02-24 | 2017-04-27 | Hoeganaes Corporation | Lubricant System For Use In Powder Metallurgy |
US11939477B2 (en) | 2014-01-30 | 2024-03-26 | Monolith Materials, Inc. | High temperature heat integration method of making carbon black |
US11203692B2 (en) | 2014-01-30 | 2021-12-21 | Monolith Materials, Inc. | Plasma gas throat assembly and method |
US10370539B2 (en) | 2014-01-30 | 2019-08-06 | Monolith Materials, Inc. | System for high temperature chemical processing |
US11591477B2 (en) | 2014-01-30 | 2023-02-28 | Monolith Materials, Inc. | System for high temperature chemical processing |
US11866589B2 (en) | 2014-01-30 | 2024-01-09 | Monolith Materials, Inc. | System for high temperature chemical processing |
US11304288B2 (en) | 2014-01-31 | 2022-04-12 | Monolith Materials, Inc. | Plasma torch design |
US20170029929A1 (en) * | 2014-05-31 | 2017-02-02 | Element Six Gmbh | Method of coating a body, granules for the method and method of making granules |
US10781512B2 (en) * | 2014-05-31 | 2020-09-22 | Element Six Gmbh | Method of coating a body, granules for the method and method of making granules |
US11987712B2 (en) | 2015-02-03 | 2024-05-21 | Monolith Materials, Inc. | Carbon black generating system |
US10618026B2 (en) | 2015-02-03 | 2020-04-14 | Monolith Materials, Inc. | Regenerative cooling method and apparatus |
US11998886B2 (en) | 2015-02-03 | 2024-06-04 | Monolith Materials, Inc. | Regenerative cooling method and apparatus |
US11665808B2 (en) | 2015-07-29 | 2023-05-30 | Monolith Materials, Inc. | DC plasma torch electrical power design method and apparatus |
US12119133B2 (en) | 2015-09-09 | 2024-10-15 | Monolith Materials, Inc. | Circular few layer graphene |
US10808097B2 (en) | 2015-09-14 | 2020-10-20 | Monolith Materials, Inc. | Carbon black from natural gas |
US11492496B2 (en) | 2016-04-29 | 2022-11-08 | Monolith Materials, Inc. | Torch stinger method and apparatus |
US11149148B2 (en) | 2016-04-29 | 2021-10-19 | Monolith Materials, Inc. | Secondary heat addition to particle production process and apparatus |
US12012515B2 (en) | 2016-04-29 | 2024-06-18 | Monolith Materials, Inc. | Torch stinger method and apparatus |
US11926743B2 (en) | 2017-03-08 | 2024-03-12 | Monolith Materials, Inc. | Systems and methods of making carbon particles with thermal transfer gas |
US11760884B2 (en) | 2017-04-20 | 2023-09-19 | Monolith Materials, Inc. | Carbon particles having high purities and methods for making same |
EP3676335A4 (en) * | 2017-08-28 | 2021-03-31 | Monolith Materials, Inc. | Particle systems and methods |
CN111278928A (en) * | 2017-08-28 | 2020-06-12 | 巨石材料公司 | Particle system and method |
WO2019046324A1 (en) * | 2017-08-28 | 2019-03-07 | Monolith Materials, Inc. | Particle systems and methods |
US20210017031A1 (en) * | 2017-08-28 | 2021-01-21 | Monolith Materials, Inc. | Particle systems and methods |
US12030776B2 (en) | 2017-08-28 | 2024-07-09 | Monolith Materials, Inc. | Systems and methods for particle generation |
US11453784B2 (en) | 2017-10-24 | 2022-09-27 | Monolith Materials, Inc. | Carbon particles having specific contents of polycylic aromatic hydrocarbon and benzo[a]pyrene |
Also Published As
Publication number | Publication date |
---|---|
EP1246949B1 (en) | 2006-02-08 |
DE60025931T2 (en) | 2006-08-31 |
KR100697534B1 (en) | 2007-03-20 |
AU7758000A (en) | 2001-05-14 |
JP2003514112A (en) | 2003-04-15 |
DE60025931D1 (en) | 2006-04-20 |
WO2001032946A1 (en) | 2001-05-10 |
MXPA02004478A (en) | 2004-09-10 |
KR20020062637A (en) | 2002-07-26 |
EP1246949A4 (en) | 2004-04-14 |
ATE317458T1 (en) | 2006-02-15 |
EP1246949A1 (en) | 2002-10-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1246949B1 (en) | Method of making an improved metallurgical powder compositions and using the same | |
US6068813A (en) | Method of making powder metallurgical compositions | |
EP1218131B1 (en) | Improved metal-based powder compositions containing silicon carbide as an alloying powder | |
CA2569973C (en) | Powder metallurgical compositions and parts made therefrom | |
US8992659B2 (en) | Metal powder composition | |
US7527667B2 (en) | Powder metallurgical compositions and methods for making the same | |
US4927461A (en) | Machinable-grade, ferrous powder blend containing boron nitride and method thereof | |
EP1476264B1 (en) | Improved powder metallurgy lubricant compositions and methods for using the same | |
CA2832433A1 (en) | Vanadium-containing powder metallurgical powders and methods of their use | |
US5938814A (en) | Iron based powder mixture for powder metallurgy | |
KR20180008732A (en) | Mixed powder for iron powder metallurgy, method for producing the same, sintered body made using the same and method for producing the same | |
CA1327462C (en) | Machinable-grade, ferrous powder blend containing boron nitride |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |