CA2572130C - Stainless steel powder - Google Patents
Stainless steel powder Download PDFInfo
- Publication number
- CA2572130C CA2572130C CA2572130A CA2572130A CA2572130C CA 2572130 C CA2572130 C CA 2572130C CA 2572130 A CA2572130 A CA 2572130A CA 2572130 A CA2572130 A CA 2572130A CA 2572130 C CA2572130 C CA 2572130C
- Authority
- CA
- Canada
- Prior art keywords
- stainless steel
- steel powder
- powder
- vanadium
- sintered
- 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.)
- Expired - Fee Related
Links
- 239000000843 powder Substances 0.000 title claims abstract description 63
- 229910001220 stainless steel Inorganic materials 0.000 title claims abstract description 41
- 239000010935 stainless steel Substances 0.000 title claims abstract description 32
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 44
- 239000000203 mixture Substances 0.000 claims abstract description 27
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 24
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 21
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 19
- 239000011651 chromium Substances 0.000 claims abstract description 19
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims abstract description 19
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 18
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 18
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 13
- 239000010703 silicon Substances 0.000 claims abstract description 11
- 229910000831 Steel Inorganic materials 0.000 claims abstract description 9
- 239000010959 steel Substances 0.000 claims abstract description 9
- 238000005245 sintering Methods 0.000 claims description 21
- 239000000314 lubricant Substances 0.000 claims description 15
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 14
- 229910052759 nickel Inorganic materials 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 5
- 239000000654 additive Substances 0.000 claims description 3
- 238000005275 alloying Methods 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 239000004129 EU approved improving agent Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 238000005056 compaction Methods 0.000 description 18
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 229910052758 niobium Inorganic materials 0.000 description 8
- 239000010955 niobium Substances 0.000 description 8
- -1 chromium carbides Chemical class 0.000 description 6
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 6
- 238000000137 annealing Methods 0.000 description 5
- 239000011159 matrix material Substances 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052748 manganese Inorganic materials 0.000 description 4
- 239000011572 manganese Substances 0.000 description 4
- ZLANVVMKMCTKMT-UHFFFAOYSA-N methanidylidynevanadium(1+) Chemical class [V+]#[C-] ZLANVVMKMCTKMT-UHFFFAOYSA-N 0.000 description 4
- 150000004767 nitrides Chemical class 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000005265 energy consumption Methods 0.000 description 3
- 229910052750 molybdenum Inorganic materials 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 239000004610 Internal Lubricant Substances 0.000 description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000011733 molybdenum Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 229940053200 antiepileptics fatty acid derivative Drugs 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 229910001634 calcium fluoride Inorganic materials 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007596 consolidation process Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- HGPXWXLYXNVULB-UHFFFAOYSA-M lithium stearate Chemical compound [Li+].CCCCCCCCCCCCCCCCCC([O-])=O HGPXWXLYXNVULB-UHFFFAOYSA-M 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- RKISUIUJZGSLEV-UHFFFAOYSA-N n-[2-(octadecanoylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCNC(=O)CCCCCCCCCCCCCCCCC RKISUIUJZGSLEV-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000004663 powder metallurgy Methods 0.000 description 1
- 238000004881 precipitation hardening Methods 0.000 description 1
- 239000012925 reference material Substances 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- CADICXFYUNYKGD-UHFFFAOYSA-N sulfanylidenemanganese Chemical compound [Mn]=S CADICXFYUNYKGD-UHFFFAOYSA-N 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/02—Making ferrous alloys by powder metallurgy
- C22C33/0257—Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements
- C22C33/0278—Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements with at least one alloying element having a minimum content above 5%
- C22C33/0285—Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements with at least one alloying element having a minimum content above 5% with Cr, Co, or Ni having a minimum content higher than 5%
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
- B22F1/10—Metallic powder containing lubricating or binding agents; Metallic powder containing organic material
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/24—Ferrous alloys, e.g. steel alloys containing chromium with vanadium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2998/00—Supplementary information concerning processes or compositions relating to powder metallurgy
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2998/00—Supplementary information concerning processes or compositions relating to powder metallurgy
- B22F2998/10—Processes characterised by the sequence of their steps
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Powder Metallurgy (AREA)
- Materials For Medical Uses (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Abstract
The invention concerns a stainless steel powder and composition comprising at least 10w-t% chromium. Vanadium is present in an amount of at least 4 times the amount of carbon and nitrogen. The steel powder comprises 10-30% chromium, 0.1-1.0 vanadium, 0.5-1.5% silicon, less than 0.1% carbon and less than 0.07%
nitrogen. A process for preparing a sintered part and a sintered part are also claimed.
nitrogen. A process for preparing a sintered part and a sintered part are also claimed.
Description
STAINLESS STEEL POWDER
FIELD OF THE INVENTION
The present invention concerns a new stainless steel powder and stainless steel powder compositions including this new powder. Specifically the invention concerns stainless steel powder compositions for manufacturing sintered powder metallurgical parts having high densities.
BACKGROUND OF THE INVENTION
A primary goal in powder metallurgy is to achieve high density of compacted and sintered bodies. There are several methods of improving density, one of those methods is warm compaction which improves the compressibility of the powder giving a green body with higher green density. By applying die wall lubrication, which makes it possible to minimise the amount of internal lubricants used, the green density may also be increased. The use of high compaction pressures in combination with low amounts of lubricants also results in elevated green densities. Soft annealing of a stainless steel powder, where the material is strain relieved and recrystallized, also improves the compressibility. After compaction the green body is subjected to a sintering operation in order to achieve a sintered body. High temperatures at sintering, i.e. above about 1180-1200 C lead to increased shrinkage during sintering and higher density of the body. However, high temperature sintering requires specially equipped sintering furnaces. Additionally the energy consumption will be increased.
Special problems are encountered when high density, stainless steel PM parts are manufactured due to the presence of chromium, which makes the steel resistant to corrosion.
Stainless steels have approximately above 10% chromium.
Most often carbon is present in steels and will cause formation of chromium carbides. The formation of chromium carbides lowers the chromium content in the matrix, which in turn causes lower corrosion resistance. In order to avoid that the chromium content in the matrix is reduced, carbide forming stabilizers, such as niobium, are often used. In this way the formation of chromium carbides can be avoided and instead niobium carbides are formed, a result of which is that the corrosion resistance can be maintained. However, a problem with the use of niobium is that high sintering temperatures are necessary for obtaining high sintered densities and the energy consumption is considerable.
It has now been found that, by using the new powder according to the present invention, the energy costs for producing sintered stainless steel PM parts can be reduced. Another significant advantage of using the new powder is that a comparatively higher sintered density can be obtained.
The sintered parts manufactured by using the new powder are of particularly interest within the automotive industry where the demands on both costs and performance of the parts are high. The new powder can also be used for sintered parts in exhaust systems, and especially for flanges in exhaust systems.
The present invention concerns stainless steel powder, stainless steel powder compositions as well as the compacted and sintered parts obtained thereof having high densities. Specifically the invention concerns stainless steel powder compositions for manufacturing powder metallurgical parts.
SUMMARY OF THE INVENTION
It has now surprisingly been found that, by adding vanadium as a stabiliser to a stainless steel powder, the sintering temperature and accordingly the energy consumption can be reduced, while the sintered density is similar or even increased in comparison with the presently used niobium stabiliser. Furthermore it has been found that the vanadium should be present in an amount of at least 4 times the combined amounts of carbon and nitrogen, whereby the amount of nitrogen should be less than 0.07% by weight and the amount of carbon should be less than 0.1% by weight. The amount of vanadium should be in the range of 0A-1o by weight.
Stainless steel compositions including vanadium are disclosed in WO 03/106077 publication and in the US
patent 5 856 625. In WO 03/106077 there is not disclosed any effect or any actual examples of powders including vanadium. According to the US patent 5 856 625 the stainless steel powder preferably comprises 1.5-2.5%
vanadium. This known stainless steel powder is intended for materials with high wear resistance and a high carbon content is necessary to achieve a proper amount of hard carbides in the matrix formed mainly from strong carbide forming elements such as Mo, V and W. Also the patent publication JP 59-47358 discloses a steel powder is comprising chromium, silicon, carbon and nitrogen. This powder may further contain nickel and/or copper and vanadium. The purpose of the the steel powder according to JP 59-47358 is to manufacture e.g. a sliding surface.
FIELD OF THE INVENTION
The present invention concerns a new stainless steel powder and stainless steel powder compositions including this new powder. Specifically the invention concerns stainless steel powder compositions for manufacturing sintered powder metallurgical parts having high densities.
BACKGROUND OF THE INVENTION
A primary goal in powder metallurgy is to achieve high density of compacted and sintered bodies. There are several methods of improving density, one of those methods is warm compaction which improves the compressibility of the powder giving a green body with higher green density. By applying die wall lubrication, which makes it possible to minimise the amount of internal lubricants used, the green density may also be increased. The use of high compaction pressures in combination with low amounts of lubricants also results in elevated green densities. Soft annealing of a stainless steel powder, where the material is strain relieved and recrystallized, also improves the compressibility. After compaction the green body is subjected to a sintering operation in order to achieve a sintered body. High temperatures at sintering, i.e. above about 1180-1200 C lead to increased shrinkage during sintering and higher density of the body. However, high temperature sintering requires specially equipped sintering furnaces. Additionally the energy consumption will be increased.
Special problems are encountered when high density, stainless steel PM parts are manufactured due to the presence of chromium, which makes the steel resistant to corrosion.
Stainless steels have approximately above 10% chromium.
Most often carbon is present in steels and will cause formation of chromium carbides. The formation of chromium carbides lowers the chromium content in the matrix, which in turn causes lower corrosion resistance. In order to avoid that the chromium content in the matrix is reduced, carbide forming stabilizers, such as niobium, are often used. In this way the formation of chromium carbides can be avoided and instead niobium carbides are formed, a result of which is that the corrosion resistance can be maintained. However, a problem with the use of niobium is that high sintering temperatures are necessary for obtaining high sintered densities and the energy consumption is considerable.
It has now been found that, by using the new powder according to the present invention, the energy costs for producing sintered stainless steel PM parts can be reduced. Another significant advantage of using the new powder is that a comparatively higher sintered density can be obtained.
The sintered parts manufactured by using the new powder are of particularly interest within the automotive industry where the demands on both costs and performance of the parts are high. The new powder can also be used for sintered parts in exhaust systems, and especially for flanges in exhaust systems.
The present invention concerns stainless steel powder, stainless steel powder compositions as well as the compacted and sintered parts obtained thereof having high densities. Specifically the invention concerns stainless steel powder compositions for manufacturing powder metallurgical parts.
SUMMARY OF THE INVENTION
It has now surprisingly been found that, by adding vanadium as a stabiliser to a stainless steel powder, the sintering temperature and accordingly the energy consumption can be reduced, while the sintered density is similar or even increased in comparison with the presently used niobium stabiliser. Furthermore it has been found that the vanadium should be present in an amount of at least 4 times the combined amounts of carbon and nitrogen, whereby the amount of nitrogen should be less than 0.07% by weight and the amount of carbon should be less than 0.1% by weight. The amount of vanadium should be in the range of 0A-1o by weight.
Stainless steel compositions including vanadium are disclosed in WO 03/106077 publication and in the US
patent 5 856 625. In WO 03/106077 there is not disclosed any effect or any actual examples of powders including vanadium. According to the US patent 5 856 625 the stainless steel powder preferably comprises 1.5-2.5%
vanadium. This known stainless steel powder is intended for materials with high wear resistance and a high carbon content is necessary to achieve a proper amount of hard carbides in the matrix formed mainly from strong carbide forming elements such as Mo, V and W. Also the patent publication JP 59-47358 discloses a steel powder is comprising chromium, silicon, carbon and nitrogen. This powder may further contain nickel and/or copper and vanadium. The purpose of the the steel powder according to JP 59-47358 is to manufacture e.g. a sliding surface.
DETAILED DESCRIPTION OF THE INVENTION
Specifically, the stainless steel powder according to the invention comprises 10-30% chromium, 0.1-1% vanadium, 0.5-1.5% silicon, less than 0.1% carbon and less than 0.07% nitrogen. Preferably the stainless steel powder comprises 10-20% chromium, 0.15-0.8% vanadium, 0.7-1.2%
silicon, less than 0.05% carbon and less than 0.05%
nitrogen.
As the corrosion resistance in stainless steels is of great interest the vanadium content should be chosen so that vanadium carbides and nitrides are formed instead of chromium carbides and nitrides. Preferably the vanadium content will be chosen in relation to the actual carbon and nitrogen content in the sintered component to be able to form vanadium carbides and nitrides. It is believed that the vanadium carbides and nitrides formed are of type VC and NC and according to our present knowledge the vanadium content should preferably be minimum 4 times the carbon and nitrogen content of the powder. The actual carbon and nitrogen content in the sintered component may be higher than the content of the elements in the powder due to pick up during delubrication.
The amount of silicon should be between 0.5% to 1.5%.
Silicon is an important element as it creates a thin coherent oxide layer during atomisation of the stainless steel melt, i.e. the silicon content should be 0.5% by weight or above. The oxide layer prevents further oxidation. A too high silicon level will lead to a decrease in compressibility, hence the silicon content should be 1.5% by weight or lower.
The amount of nitrogen should be as low as possible as nitrogen can have the same influence as carbon, i.e.
sensitising the material through formation of chromium nitrides or chromium carbonitrides. Nitrogen has also a precipitation hardening effect which will decrease the compressibility. Therefore the nitrogen content should not exceed 0.07%, preferably not 0.05% by weight. In 5 practice it is difficult to obtain nitrogen contents lower than 0.001%.
Other alloying elements are added to enhance certain properties, such as strength, hardness etc. The alloying elements are selected from the group consisting of molybdenum, copper, manganese and nickel.
According to the present invention ferrit.ic stainless steels are preferred. Ferritic stainless steels are less expensive than austenitic stainless steels which are alloyed with nickel. Compared with an austenitic matrix a ferritic matrix has a lower coefficient of thermal expansion, which is beneficial for example in flanges in a stainless steel exhaust system. Therefore a preferred embodiment of the stainless steel according to the invention is essentially free from nickel. Specifically the ferritic stainless steel may comprise 10-20% by weight of chromium, 0-5% by weight of molybdenum, less than 1% by weight of nickel, less than 0.2% by weight of manganese.
Other possible additives are flow agents, machinability improving agents such as calcium fluoride, manganese sulfide, boron nitride or combinations thereof.
The stainless steel powder may be a gas or water atomised, pre-alloyed powder having an average particle size above about 20 pm, depending on the method of consolidation of the powder. Normally the average particle size is above about 50 pm.
Specifically, the stainless steel powder according to the invention comprises 10-30% chromium, 0.1-1% vanadium, 0.5-1.5% silicon, less than 0.1% carbon and less than 0.07% nitrogen. Preferably the stainless steel powder comprises 10-20% chromium, 0.15-0.8% vanadium, 0.7-1.2%
silicon, less than 0.05% carbon and less than 0.05%
nitrogen.
As the corrosion resistance in stainless steels is of great interest the vanadium content should be chosen so that vanadium carbides and nitrides are formed instead of chromium carbides and nitrides. Preferably the vanadium content will be chosen in relation to the actual carbon and nitrogen content in the sintered component to be able to form vanadium carbides and nitrides. It is believed that the vanadium carbides and nitrides formed are of type VC and NC and according to our present knowledge the vanadium content should preferably be minimum 4 times the carbon and nitrogen content of the powder. The actual carbon and nitrogen content in the sintered component may be higher than the content of the elements in the powder due to pick up during delubrication.
The amount of silicon should be between 0.5% to 1.5%.
Silicon is an important element as it creates a thin coherent oxide layer during atomisation of the stainless steel melt, i.e. the silicon content should be 0.5% by weight or above. The oxide layer prevents further oxidation. A too high silicon level will lead to a decrease in compressibility, hence the silicon content should be 1.5% by weight or lower.
The amount of nitrogen should be as low as possible as nitrogen can have the same influence as carbon, i.e.
sensitising the material through formation of chromium nitrides or chromium carbonitrides. Nitrogen has also a precipitation hardening effect which will decrease the compressibility. Therefore the nitrogen content should not exceed 0.07%, preferably not 0.05% by weight. In 5 practice it is difficult to obtain nitrogen contents lower than 0.001%.
Other alloying elements are added to enhance certain properties, such as strength, hardness etc. The alloying elements are selected from the group consisting of molybdenum, copper, manganese and nickel.
According to the present invention ferrit.ic stainless steels are preferred. Ferritic stainless steels are less expensive than austenitic stainless steels which are alloyed with nickel. Compared with an austenitic matrix a ferritic matrix has a lower coefficient of thermal expansion, which is beneficial for example in flanges in a stainless steel exhaust system. Therefore a preferred embodiment of the stainless steel according to the invention is essentially free from nickel. Specifically the ferritic stainless steel may comprise 10-20% by weight of chromium, 0-5% by weight of molybdenum, less than 1% by weight of nickel, less than 0.2% by weight of manganese.
Other possible additives are flow agents, machinability improving agents such as calcium fluoride, manganese sulfide, boron nitride or combinations thereof.
The stainless steel powder may be a gas or water atomised, pre-alloyed powder having an average particle size above about 20 pm, depending on the method of consolidation of the powder. Normally the average particle size is above about 50 pm.
Most often a lubricant is added prior to compaction in order to enhance the compressibility of the powder and to facilitate the ejection of the green component. The amount of lubricant is typically between 0.1% and 2%, preferably between 0.3% and 1.5%. The lubricants may be chosen from the group consisting of metal sterates, such as zink or lithium stearate, Kenolube , amide polymers or amide oligomers, ethylene bisstearamide, fatty acid derivatives or other suitable substances with a lubricating effect. Die wall lubrication alone or in combination with internal lubricants may also be used.
After an optional annealing the stainless steel powder is mixed with lubricant and other optional additives. The powder mixture is compacted at 400-1200 MPa and sintered at 1150-1350 C for 5 minutes to 1 hour to obtain a density of at least 7.20 g/cm3. However, the powder according to the invention can be used for producing parts having lower sintered density in order to reduce processing costs. The compaction step could be performed as cold compaction or warm compaction.
The high sintered density is obtained by increased shrinkage during the sintering and without being bound to any specific theory, it is believed that this shrinkage is a consequence of promoted volume diffusion. Vanadium carbides which are formed in presence of carbon will be dissolved at elevated temperatures, especially at sintering temperatures, but also at lower temperatures such as at annealing of the metal powder. Normally the sintering temperature for stainless steel powders is about 1150-1300 C.
Example 1 Three different melts having a chemical composition according to table 1 and containing niobium and vanadium as carbide forming elements were produced. Several mixtures were prepared for cold or warm compaction according to table 2 and 3. For cold compaction and warm compaction purposes lubricants were used. As a flow agent in warm compaction Aerosil A-200 from Degussa was used.
Table 1. Chemical analysis of unannealed powders Batch Cr% Nb% V% Si% Mn% Ni% P% C% N% 0% S%
A 11.85 --- 0.29 0.68 0.23 0.053 0.008 0.024 0.014 0.144 0.0033 B 11.94 0.39 --- 0.68 0.23 0.051 0.010 0.025 0.011 0.152 0.0027 C 11.79 0.58 --- 0.73 0.23 0.056 0.009 0.026 0.011 0.143 0.0030 Table 2. Mixtures for cold compaction Mixture Composition no 4* A + 1% lubricant 5 B + 1% lubricant 6 C + 1% lubricant *= composition according to the invention Table 3. Mixtures for warm compaction Mixture Composition no 10* A + 1% lubricant + 0.1% A-200 11 B + 1% lubricant + 0.1% A-200 12 C + 1% lubricant + 0.1% A-200 *= composition according to the invention The powder mixtures according to table 2 and 3 were compacted and green properties were determined for various compaction pressures. The results are presented in table 4. The compacted bodies were sintered at 1250 C
in an atmosphere of hydrogen for 45 minutes and the sintered densities and mechanical properties were determined. The results are shown in table 5.
After an optional annealing the stainless steel powder is mixed with lubricant and other optional additives. The powder mixture is compacted at 400-1200 MPa and sintered at 1150-1350 C for 5 minutes to 1 hour to obtain a density of at least 7.20 g/cm3. However, the powder according to the invention can be used for producing parts having lower sintered density in order to reduce processing costs. The compaction step could be performed as cold compaction or warm compaction.
The high sintered density is obtained by increased shrinkage during the sintering and without being bound to any specific theory, it is believed that this shrinkage is a consequence of promoted volume diffusion. Vanadium carbides which are formed in presence of carbon will be dissolved at elevated temperatures, especially at sintering temperatures, but also at lower temperatures such as at annealing of the metal powder. Normally the sintering temperature for stainless steel powders is about 1150-1300 C.
Example 1 Three different melts having a chemical composition according to table 1 and containing niobium and vanadium as carbide forming elements were produced. Several mixtures were prepared for cold or warm compaction according to table 2 and 3. For cold compaction and warm compaction purposes lubricants were used. As a flow agent in warm compaction Aerosil A-200 from Degussa was used.
Table 1. Chemical analysis of unannealed powders Batch Cr% Nb% V% Si% Mn% Ni% P% C% N% 0% S%
A 11.85 --- 0.29 0.68 0.23 0.053 0.008 0.024 0.014 0.144 0.0033 B 11.94 0.39 --- 0.68 0.23 0.051 0.010 0.025 0.011 0.152 0.0027 C 11.79 0.58 --- 0.73 0.23 0.056 0.009 0.026 0.011 0.143 0.0030 Table 2. Mixtures for cold compaction Mixture Composition no 4* A + 1% lubricant 5 B + 1% lubricant 6 C + 1% lubricant *= composition according to the invention Table 3. Mixtures for warm compaction Mixture Composition no 10* A + 1% lubricant + 0.1% A-200 11 B + 1% lubricant + 0.1% A-200 12 C + 1% lubricant + 0.1% A-200 *= composition according to the invention The powder mixtures according to table 2 and 3 were compacted and green properties were determined for various compaction pressures. The results are presented in table 4. The compacted bodies were sintered at 1250 C
in an atmosphere of hydrogen for 45 minutes and the sintered densities and mechanical properties were determined. The results are shown in table 5.
Table 4.
Mixture Compaction Green Green no pressure strength density (Mpa) (g/cm3) 4* 600 15.3 6.57 700 18.0 6.69 800 19.3 6.79 600 15.4 6.55 700 18.1 6.68 800 19.5 6.80 6 600 15.3 6.55 700 18.1 6.68 800 19.4 6.78 10* 600 31.3 6.73 700 37.5 6.87 800 39.9 6.96 11 600 30.1 6.71 700 36.7 6.86 800 40.4 6.96 12 600 29.4 6.71 700 34.9 6.86 800 39.4 6.96 *= composition according to the invention 5 Table 5.
Mixture Compaction Sintered Dimensional Yield Tensile no pressure density change strength strength (MPa) (g/cm3) (o) (MPa) (MPa) 4* 600 7.36 -3.87 222 390 700 7.42 -3.29 216 409 800 7.45 -2.71 215 405 5 600 7.24 -3.48 204 366 700 7.31 -3.09 208 375 800 7.38 -2.82 228 384 6 600 7.10 -2.85 202 356 700 7.20 -2.55 208 366 800 7.26 -2.30 213 376 10* 600 7.42 -3.38 221 420 700 7.47 -2.67 230 434 800 7.49 -2.20 234 431 11 600 7.28 -2.93 206 371 700 7.36 -2.52 210 386 800 7.43 -2.20 216 400 12 600 7.16 -2.36 203 361 700 7.27 -2.05 212 377 800 7.33 -1.79 214 389 *= composition according to the invention From table 4 and table 5 it can clearly be identified that the sintered densities of the samples produced from the material according to the invention are improved, while the green densities of the material according to the invention are similar to the comparative materials.
The mechanical properties of the sintered components are also improved with material according to the invention compared with known materials.
Example 2 In order to evaluate the influence of sintering temperatures and sintering times, powder mixtures 4, 5 and 6 were compacted into tensile test samples according to ISO 2740 in a uniaxially compaction movement at ambient temperature at 600 MPa. The obtained green samples were sintered at 1200 C, 1250 C and 1300 C in an atmosphere of hydrogen for 20 minutes and 45 minutes, respectively.
After sintering the sintered density of the sintered samples were measured according to ISO 3369. The results are shown in table 6. From table 6 it can be concluded that sintered densities above 7.2 g/cm3 can be obtained for a ferritic stainless steel powder provided vanadium is added, even at a sintering temperature as low as 1200 C. A sintering time of 20 minutes at a sintering temperature of 1250 C yields a sintered density of 7.35 g/cm3, whereas the corresponding density for the niobium stabilized ferritic stainless steel powder is 7.15 g/cm3 and 7.03 g/cm3 respectively, depending on the amount of niobium added.
The example reveals a surprisingly great impact on the shrinkage during sintering of a green body produced from ferritic stainless steel powder according to the invention.
Table 6.
Mixture Sintering Sintered densities (g/cm3) at no time (min) different sintering temperatures 4* 45 7.29 7.36 7.46 5 45 7.03 7.24 7.47 6 45 6.92 7.1 7.38 4* 20 - 7.35 -5 20 - 7.16 -6 20 - 7.03 -*= composition according to the invention 5 Example 3 In order to evaluate the influence of the nitrogen content of the stainless steel powder one melt was atomised and powder samples having different nitrogen 10 content were prepared from the atomised powder by annealing in a nitrogen-containing atmosphere. As reference material powder annealed in an atmosphere of 100 % of hydrogen was used. The powder samples were mixed with 1% lubricant and the obtained compositions were cold compacted at different pressures into specimens. The specimens were sintered at 1250 C in an atmosphere of hydrogen for 45 minutes. The chemical analysis of the different powder samples is presented in table 7 except the nitrogen content, which was determined after annealing as presented in table 8. In table 8 the sintered density is presented for different specimens.
Mixture Compaction Green Green no pressure strength density (Mpa) (g/cm3) 4* 600 15.3 6.57 700 18.0 6.69 800 19.3 6.79 600 15.4 6.55 700 18.1 6.68 800 19.5 6.80 6 600 15.3 6.55 700 18.1 6.68 800 19.4 6.78 10* 600 31.3 6.73 700 37.5 6.87 800 39.9 6.96 11 600 30.1 6.71 700 36.7 6.86 800 40.4 6.96 12 600 29.4 6.71 700 34.9 6.86 800 39.4 6.96 *= composition according to the invention 5 Table 5.
Mixture Compaction Sintered Dimensional Yield Tensile no pressure density change strength strength (MPa) (g/cm3) (o) (MPa) (MPa) 4* 600 7.36 -3.87 222 390 700 7.42 -3.29 216 409 800 7.45 -2.71 215 405 5 600 7.24 -3.48 204 366 700 7.31 -3.09 208 375 800 7.38 -2.82 228 384 6 600 7.10 -2.85 202 356 700 7.20 -2.55 208 366 800 7.26 -2.30 213 376 10* 600 7.42 -3.38 221 420 700 7.47 -2.67 230 434 800 7.49 -2.20 234 431 11 600 7.28 -2.93 206 371 700 7.36 -2.52 210 386 800 7.43 -2.20 216 400 12 600 7.16 -2.36 203 361 700 7.27 -2.05 212 377 800 7.33 -1.79 214 389 *= composition according to the invention From table 4 and table 5 it can clearly be identified that the sintered densities of the samples produced from the material according to the invention are improved, while the green densities of the material according to the invention are similar to the comparative materials.
The mechanical properties of the sintered components are also improved with material according to the invention compared with known materials.
Example 2 In order to evaluate the influence of sintering temperatures and sintering times, powder mixtures 4, 5 and 6 were compacted into tensile test samples according to ISO 2740 in a uniaxially compaction movement at ambient temperature at 600 MPa. The obtained green samples were sintered at 1200 C, 1250 C and 1300 C in an atmosphere of hydrogen for 20 minutes and 45 minutes, respectively.
After sintering the sintered density of the sintered samples were measured according to ISO 3369. The results are shown in table 6. From table 6 it can be concluded that sintered densities above 7.2 g/cm3 can be obtained for a ferritic stainless steel powder provided vanadium is added, even at a sintering temperature as low as 1200 C. A sintering time of 20 minutes at a sintering temperature of 1250 C yields a sintered density of 7.35 g/cm3, whereas the corresponding density for the niobium stabilized ferritic stainless steel powder is 7.15 g/cm3 and 7.03 g/cm3 respectively, depending on the amount of niobium added.
The example reveals a surprisingly great impact on the shrinkage during sintering of a green body produced from ferritic stainless steel powder according to the invention.
Table 6.
Mixture Sintering Sintered densities (g/cm3) at no time (min) different sintering temperatures 4* 45 7.29 7.36 7.46 5 45 7.03 7.24 7.47 6 45 6.92 7.1 7.38 4* 20 - 7.35 -5 20 - 7.16 -6 20 - 7.03 -*= composition according to the invention 5 Example 3 In order to evaluate the influence of the nitrogen content of the stainless steel powder one melt was atomised and powder samples having different nitrogen 10 content were prepared from the atomised powder by annealing in a nitrogen-containing atmosphere. As reference material powder annealed in an atmosphere of 100 % of hydrogen was used. The powder samples were mixed with 1% lubricant and the obtained compositions were cold compacted at different pressures into specimens. The specimens were sintered at 1250 C in an atmosphere of hydrogen for 45 minutes. The chemical analysis of the different powder samples is presented in table 7 except the nitrogen content, which was determined after annealing as presented in table 8. In table 8 the sintered density is presented for different specimens.
Table 7 Batch Cro Nbo V% Si% Mn% Ni% P% Co S%
D 12.14 0.01 0.29 0.83 0.13 0.05 0.001 0.017 0.012 Table 8 Compaction Sintered pressure Density Batch (MPa) %N (g/cm3 Dl 600 7.18 Dl 700 0.056 7.28 Dl 800 7.36 D2 600 7.13 D2 700 0.072 7.24 D2 800 7.31 D(ref) 600 7.23 D(ref) 700 0.019 7.34 D(ref) 800 7.39 It can be seen from example 3 that a nitrogen content above 0.07% will result in undesired sintered density.
D 12.14 0.01 0.29 0.83 0.13 0.05 0.001 0.017 0.012 Table 8 Compaction Sintered pressure Density Batch (MPa) %N (g/cm3 Dl 600 7.18 Dl 700 0.056 7.28 Dl 800 7.36 D2 600 7.13 D2 700 0.072 7.24 D2 800 7.31 D(ref) 600 7.23 D(ref) 700 0.019 7.34 D(ref) 800 7.39 It can be seen from example 3 that a nitrogen content above 0.07% will result in undesired sintered density.
Claims (8)
1. A pre-alloyed stainless steel powder comprising at least 10% by weight of chromium, less than 0.1% by weight of carbon and less than 0.07% by weight of nitrogen, said powder further comprising vanadium in an amount of at least 4 times the combined amounts of carbon and nitrogen, wherein the amount of vanadium is 0.1-1% by weight.
2. The stainless steel powder according to claim 1, wherein the steel powder further comprises 10-30%
chromium and 0.5-1.5% silicon.
chromium and 0.5-1.5% silicon.
3. The stainless steel powder according to claim 1 or 2, wherein the steel powder comprises 10-20%
chromium, 0.15-0.8% vanadium, 0.7-1.2% silicon, less than 0.05% carbon and less than 0.05%
nitrogen.
chromium, 0.15-0.8% vanadium, 0.7-1.2% silicon, less than 0.05% carbon and less than 0.05%
nitrogen.
4. The stainless steel powder according to claim 1, 2 or 3, wherein the steel powder is essentially free from nickel.
5. A powder metallurgical composition comprising a stainless steel powder according to anyone of the preceding claims and additives selected from the group consisting of lubricants, flow agents, machinability improving agents and alloying elements.
6. A process of preparing compacted parts of stainless steel powder comprising the steps of:
- subjecting a steel powder according to anyone of claims 1 to 4 optionally mixed with a lubricant - sintering the compacted part at a temperature of 1150-1350°C.
- subjecting a steel powder according to anyone of claims 1 to 4 optionally mixed with a lubricant - sintering the compacted part at a temperature of 1150-1350°C.
7. The process according to claim 6, wherein sintering is made to a density of at least 7.20 g/cm3
8. A sintered part of stainless steel powder according to anyone of claims 1 to 4, having a sintered density of at least 7.20 g/cm3.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE0401707A SE0401707D0 (en) | 2004-07-02 | 2004-07-02 | Stainless steel powder |
SE0401707-5 | 2004-07-02 | ||
PCT/SE2005/001086 WO2006004529A1 (en) | 2004-07-02 | 2005-07-01 | Stainless steel powder |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2572130A1 CA2572130A1 (en) | 2006-01-12 |
CA2572130C true CA2572130C (en) | 2011-01-18 |
Family
ID=32733732
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2572130A Expired - Fee Related CA2572130C (en) | 2004-07-02 | 2005-07-01 | Stainless steel powder |
Country Status (17)
Country | Link |
---|---|
EP (1) | EP1768803B1 (en) |
JP (1) | JP4580984B2 (en) |
CN (1) | CN101124058B (en) |
AT (1) | ATE483541T1 (en) |
AU (1) | AU2005260139B2 (en) |
BR (1) | BRPI0512943A (en) |
CA (1) | CA2572130C (en) |
DE (1) | DE602005023998D1 (en) |
DK (1) | DK1768803T3 (en) |
ES (1) | ES2354019T3 (en) |
MX (1) | MXPA06015244A (en) |
RU (1) | RU2345866C2 (en) |
SE (1) | SE0401707D0 (en) |
TW (1) | TWI279268B (en) |
UA (1) | UA83145C2 (en) |
WO (1) | WO2006004529A1 (en) |
ZA (1) | ZA200700040B (en) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE489486T1 (en) * | 2006-09-22 | 2010-12-15 | Hoeganaes Ab Publ | METALLURGICAL POWDER COMPOSITION AND PRODUCTION METHOD THEREOF |
JP5461187B2 (en) | 2006-09-22 | 2014-04-02 | ホガナス アクチボラグ (パブル) | Metallurgical powder composition and production method |
JP5902091B2 (en) * | 2009-10-16 | 2016-04-13 | ホガナス アクチボラゲット | Nitrogen-containing low nickel sintered stainless steel |
US20130136646A1 (en) * | 2010-06-04 | 2013-05-30 | Hoganas Ab (Publ) | Nitrided sintered steels |
TWI421376B (en) * | 2011-01-28 | 2014-01-01 | Taiwan Powder Technologies Co Ltd | Method of Improving Strength and Hardness of Powder Metallurgy Stainless Steel |
TWI421375B (en) * | 2011-01-28 | 2014-01-01 | Taiwan Powder Technologies Co Ltd | Methods for improving the mechanical properties of non - Austrian iron - based stainless steel surfaces |
TWI421374B (en) * | 2011-01-28 | 2014-01-01 | Taiwan Powder Technologies Co Ltd | Stainless steel low temperature carburizing method |
CN102660709A (en) * | 2012-04-24 | 2012-09-12 | 邓湘凌 | High-strength wear-resisting alloy and preparation method thereof |
DE102012216052A1 (en) * | 2012-09-11 | 2014-04-10 | Robert Bosch Gmbh | Sintered pressing part and method for producing such |
CN103643160B (en) * | 2013-11-11 | 2016-01-20 | 常熟市迅达粉末冶金有限公司 | A kind of high-performance 17-4PH stainless steel and preparation method thereof |
JP6314842B2 (en) * | 2015-01-06 | 2018-04-25 | セイコーエプソン株式会社 | Metal powder for powder metallurgy, compound, granulated powder and sintered body |
JP6314846B2 (en) * | 2015-01-09 | 2018-04-25 | セイコーエプソン株式会社 | Metal powder for powder metallurgy, compound, granulated powder and sintered body |
JP6319121B2 (en) * | 2015-01-29 | 2018-05-09 | セイコーエプソン株式会社 | Method for producing metal powder for powder metallurgy, compound, granulated powder and sintered body |
JP6314866B2 (en) * | 2015-02-09 | 2018-04-25 | セイコーエプソン株式会社 | Method for producing metal powder for powder metallurgy, compound, granulated powder and sintered body |
RU2750720C1 (en) * | 2020-04-18 | 2021-07-01 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Юго-Западный государственный университет" (ЮЗГУ) | Method of obtaining a sintered product from powder corrosive steel |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5947358A (en) * | 1982-09-08 | 1984-03-17 | Kawasaki Steel Corp | Steel powder for wear resistant sintered alloy |
ZA938889B (en) * | 1992-12-07 | 1994-08-01 | Mintek | Stainless steel composition |
ES2140066T3 (en) * | 1995-03-10 | 2000-02-16 | Powdrex Ltd | STAINLESS STEEL POWDERS AND ARTICLES PRODUCED THEREOF BY POWDER METALLURGY. |
JP4975916B2 (en) * | 2001-09-21 | 2012-07-11 | 株式会社日立製作所 | High toughness and high strength ferritic steel and its manufacturing method |
SE0201825D0 (en) * | 2002-06-14 | 2002-06-14 | Hoeganaes Ab | Hot compaction or steel powders |
-
2004
- 2004-07-02 SE SE0401707A patent/SE0401707D0/en unknown
-
2005
- 2005-07-01 WO PCT/SE2005/001086 patent/WO2006004529A1/en active Application Filing
- 2005-07-01 UA UAA200701061A patent/UA83145C2/en unknown
- 2005-07-01 AT AT05755291T patent/ATE483541T1/en not_active IP Right Cessation
- 2005-07-01 JP JP2007519170A patent/JP4580984B2/en not_active Expired - Fee Related
- 2005-07-01 DE DE602005023998T patent/DE602005023998D1/en active Active
- 2005-07-01 RU RU2007104054/02A patent/RU2345866C2/en not_active IP Right Cessation
- 2005-07-01 EP EP05755291A patent/EP1768803B1/en not_active Not-in-force
- 2005-07-01 ZA ZA200700040A patent/ZA200700040B/en unknown
- 2005-07-01 TW TW094122382A patent/TWI279268B/en not_active IP Right Cessation
- 2005-07-01 MX MXPA06015244A patent/MXPA06015244A/en active IP Right Grant
- 2005-07-01 CA CA2572130A patent/CA2572130C/en not_active Expired - Fee Related
- 2005-07-01 ES ES05755291T patent/ES2354019T3/en active Active
- 2005-07-01 CN CN2005800217987A patent/CN101124058B/en not_active Expired - Fee Related
- 2005-07-01 DK DK05755291.1T patent/DK1768803T3/en active
- 2005-07-01 BR BRPI0512943-5A patent/BRPI0512943A/en not_active IP Right Cessation
- 2005-07-01 AU AU2005260139A patent/AU2005260139B2/en not_active Ceased
Also Published As
Publication number | Publication date |
---|---|
BRPI0512943A (en) | 2008-04-15 |
DK1768803T3 (en) | 2011-01-31 |
CN101124058A (en) | 2008-02-13 |
ES2354019T3 (en) | 2011-03-09 |
AU2005260139B2 (en) | 2009-09-03 |
CA2572130A1 (en) | 2006-01-12 |
TW200605972A (en) | 2006-02-16 |
WO2006004529A1 (en) | 2006-01-12 |
RU2007104054A (en) | 2008-08-10 |
TWI279268B (en) | 2007-04-21 |
AU2005260139A1 (en) | 2006-01-12 |
SE0401707D0 (en) | 2004-07-02 |
MXPA06015244A (en) | 2007-03-15 |
UA83145C2 (en) | 2008-06-10 |
JP4580984B2 (en) | 2010-11-17 |
EP1768803A1 (en) | 2007-04-04 |
RU2345866C2 (en) | 2009-02-10 |
ATE483541T1 (en) | 2010-10-15 |
JP2008505248A (en) | 2008-02-21 |
EP1768803B1 (en) | 2010-10-06 |
ZA200700040B (en) | 2008-06-25 |
CN101124058B (en) | 2010-06-16 |
DE602005023998D1 (en) | 2010-11-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2285996B1 (en) | Iron- based pre-alloyed powder | |
KR101673484B1 (en) | Low alloyed steel powder | |
RU2553794C2 (en) | Nitrogen-containing, low-nickel sintered stainless steel | |
CA2572130C (en) | Stainless steel powder | |
JP5671526B2 (en) | High strength low alloy sintered steel | |
JP5453251B2 (en) | Iron-based powder and composition thereof | |
CA2755568C (en) | Iron vanadium powder alloy | |
EP1513640A1 (en) | Prealloyed iron-based powder, a method of producing sintered components and a component | |
GB2237029A (en) | Sintered alloy body | |
KR102012950B1 (en) | Hot-work tool steel and a process for making a hot-work tool steel | |
JP2011094187A (en) | Method for producing high strength iron based sintered compact | |
KR20020012609A (en) | Powder metallurgy manufactured high speed steel | |
US7473295B2 (en) | Stainless steel powder | |
JP4556755B2 (en) | Powder mixture for powder metallurgy | |
KR100846047B1 (en) | Stainless steel powder | |
JP2007169736A (en) | Alloy steel powder for powder metallurgy | |
EP1323840A1 (en) | Iron base mixed powder for high strength sintered parts | |
Pease | Ferrous powder metallurgy materials | |
JP2005200698A (en) | Iron-based powder mixture for high-strength sintered component | |
CN118450954A (en) | Iron-based mixed powder and iron-based sintered body for powder metallurgy | |
JP2007100115A (en) | Alloy steel powder for powder metallurgy | |
JP2007126695A (en) | Alloy steel for powder metallurgy |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
MKLA | Lapsed |
Effective date: 20130703 |