WO2018182480A1 - Hot work tool steel - Google Patents
Hot work tool steel Download PDFInfo
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- WO2018182480A1 WO2018182480A1 PCT/SE2018/050213 SE2018050213W WO2018182480A1 WO 2018182480 A1 WO2018182480 A1 WO 2018182480A1 SE 2018050213 W SE2018050213 W SE 2018050213W WO 2018182480 A1 WO2018182480 A1 WO 2018182480A1
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- 229910001315 Tool steel Inorganic materials 0.000 title abstract description 12
- 229910000831 Steel Inorganic materials 0.000 claims abstract description 106
- 239000010959 steel Substances 0.000 claims abstract description 106
- 150000001247 metal acetylides Chemical class 0.000 claims abstract description 15
- 229910000734 martensite Inorganic materials 0.000 claims abstract description 14
- 229910001563 bainite Inorganic materials 0.000 claims abstract description 9
- 239000012535 impurity Substances 0.000 claims abstract description 9
- 150000004767 nitrides Chemical class 0.000 claims abstract description 3
- 229910052720 vanadium Inorganic materials 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 10
- 229910052750 molybdenum Inorganic materials 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- 238000005496 tempering Methods 0.000 claims description 7
- 229910052804 chromium Inorganic materials 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 238000001816 cooling Methods 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- 229910052758 niobium Inorganic materials 0.000 claims description 5
- 229910052796 boron Inorganic materials 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 229910052698 phosphorus Inorganic materials 0.000 claims description 4
- 238000003303 reheating Methods 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 150000002739 metals Chemical class 0.000 claims description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 3
- 229910052742 iron Inorganic materials 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 description 12
- 239000011572 manganese Substances 0.000 description 12
- 239000011651 chromium Substances 0.000 description 11
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 11
- 238000000137 annealing Methods 0.000 description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 239000010949 copper Substances 0.000 description 6
- 239000010955 niobium Substances 0.000 description 6
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 5
- 238000007792 addition Methods 0.000 description 5
- 238000005553 drilling Methods 0.000 description 5
- 229910052748 manganese Inorganic materials 0.000 description 5
- 239000011733 molybdenum Substances 0.000 description 5
- 229910000859 α-Fe Inorganic materials 0.000 description 5
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 4
- 229910052761 rare earth metal Inorganic materials 0.000 description 4
- 150000002910 rare earth metals Chemical class 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- 239000011669 selenium Substances 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 3
- 229910052721 tungsten Inorganic materials 0.000 description 3
- 239000010937 tungsten Substances 0.000 description 3
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 239000004411 aluminium Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000004512 die casting Methods 0.000 description 2
- 238000005242 forging Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 238000005272 metallurgy Methods 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- 229910052711 selenium Inorganic materials 0.000 description 2
- 239000002893 slag Substances 0.000 description 2
- 238000009849 vacuum degassing Methods 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- VGIPUQAQWWHEMC-UHFFFAOYSA-N [V].[Mo].[Cr] Chemical compound [V].[Mo].[Cr] VGIPUQAQWWHEMC-UHFFFAOYSA-N 0.000 description 1
- 229910001566 austenite Inorganic materials 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000010891 electric arc Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- VCTOKJRTAUILIH-UHFFFAOYSA-N manganese(2+);sulfide Chemical class [S-2].[Mn+2] VCTOKJRTAUILIH-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- ZLANVVMKMCTKMT-UHFFFAOYSA-N methanidylidynevanadium(1+) Chemical class [V+]#[C-] ZLANVVMKMCTKMT-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 229910001568 polygonal ferrite Inorganic materials 0.000 description 1
- 238000004663 powder metallurgy Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000003923 scrap metal Substances 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- CADICXFYUNYKGD-UHFFFAOYSA-N sulfanylidenemanganese Chemical compound [Mn]=S CADICXFYUNYKGD-UHFFFAOYSA-N 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 description 1
- 238000009489 vacuum treatment Methods 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/002—Heat treatment of ferrous alloys containing Cr
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/18—Hardening; Quenching with or without subsequent tempering
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/26—Methods of annealing
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/005—Modifying the physical properties by deformation combined with, or followed by, heat treatment of ferrous alloys
-
- 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
- C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/12—Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/22—Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- 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
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/002—Bainite
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/008—Martensite
Definitions
- the invention relates to a hot work tool steel.
- Vanadium alloyed matrix tool steels have been on market for decades and attained a considerable interest because of the fact that they combine a high wear resistance with an excellent dimensional stability and because they have a good toughness. These steels have a wide range of applications such as for die casting and forging.
- the steels are generally produced by conventional metallurgy followed by Electro Slag Remelting (ESR).
- ESR Electro Slag Remelting
- Uddeholm DIEVAR" 9 is a high performance chromium-molybdenum-vanadium steel, containing balanced carbon and vanadium contents as described in WO 99/50468 Al. It is a modified H13 premium hot work tool steel, which is machined in the soft annealed delivery condition.
- the recommended soft annealing is heating to 850 °C in protecting atmosphere for 4 hours to obtain a uniform temperature followed by cooling at a rate of 10 °C/h to 600 °C and then freely in air. This results in a hardness of approximately 160 HB.
- the object of the present invention is to provide a hot work tool steel having an improved property profile, i.e. the inventive steel should be superior over the modified H13 tool steel known in the art in at least one respect.
- Another object of the present invention is to improve the machinability of the steel in the unhardened condition.
- Fig. 1 shows the structure of the inventive steel 800 °C/6h according to the Example.
- the length of the bar in the lower right corner is 20 ⁇ .
- Fig. 2 shows the structure of the comparative subjected to conventional soft annealing according to the Example.
- the length of the bar in the lower right corner is 20 ⁇ .
- Fig. 3 shows the structure of the inventive steel 800 °C/6h according to the Example.
- Fig. 4 shows the structure of the comparative subjected to conventional soft annealing according to the Example.
- the amount of carbon should be controlled such that the amount of primary carbides of the type M23C6, M7C3 and Me in the steel is limited, preferably the steel is free from such primary carbides.
- Si is commonly used for deoxidation. Si is present in the steel in a dissolved form and may positively influence the machinability. However, Si is a strong ferrite former and increases the carbon activity and therefore the risk for the formation of undesired carbides, which negatively affect the impact strength. Silicon is also prone to interfacial segregation, which may result in decreased toughness and thermal fatigue resistance. Si is therefore limited to 1.0 %. The upper limit may be 0.9, 0.8, 0.7, 0.6, 0.5, 0.4, 0.35 0.34, 0.32, 0.30, 0.28, 0.26, 0.24 or 0.22%. The lower limit may be 0.12, 0.14, 0.16, 0.18 and 0.20%. Preferred ranges are 0.10 - 0.25 % and 0.15 - 0.24%.
- Manganese contributes to improving the hardenability of the steel and together with sulphur manganese contributes to improving the machinability by forming manganese sulphides.
- Manganese shall therefore be present in a minimum content of 0.2 %, preferably at least 0.3, 0.35, 0.4, 0.45 or 0.5 %. At higher sulphur contents manganese prevents red brittleness in the steel.
- the steel shall contain maximum 1.0 %, preferably maximum 0.8, 0.7, 0.6, 0.55 or 0.5 %.
- Chromium is to be present in a content of at least 2.0 % in order to provide a good
- the lower limit may be 2.0, 2.5, 3.0, 3.5, 4.0, 4.1, 4.2, 4.3, 4.4, 4.5, 4.6, 4.7, 4.8 or 4.9%.
- the upper limit may be 6.0, 5.8, 5.6, 5.5, 5.4, 5.2 or 5.1 %.
- Mo is known to have a very favourable effect on the hardenability. Molybdenum is essential for attaining a good secondary hardening response. The minimum content is 1.0 %, and may be set to 1,2, 1.4, 1.6, 1.8, 2.0, 2.1, 2.2, 2.25 or 2.3 %. Molybdenum is a strong carbide forming element and also a strong ferrite former. The maximum content of molybdenum is therefore 3.5 %. Mo may be limited to 3.4, 3.3, 3.2, 3.1, 3.0, 2.9, 2.8, 2.7, 2.6, 2.5, 2.4 or 2.35 %. Vanadium (0.4 - 0.9 %)
- Vanadium forms evenly distributed primary precipitated carbides and carbonitrides of the type V(N,C) in the matrix of the steel.
- This hard phase may also be denoted MX, wherein M is mainly V but Cr and Mo may be present and X is one or more of C, N and B. Vanadium shall therefore be present in an amount of 0.4 - 0.9%.
- the upper limit may be set to 0.9, 0.8, 0.7, 0.6, 0.58, 0.56 or 0.55 %.
- the lower limit may be 0.42, 0.44, 0.46, 0.48, 0.50 or 0.52%. Aluminium (0.001 - 0.06 %)
- Aluminium is an optional element and may be used for deoxidation in combination with Si and Mn.
- the lower limit may be set to 0.001, 0.003, 0.005 or 0.007% in order to ensure a good deoxidation.
- the upper limit is restricted to 0.06% for avoiding precipitation of undesired phases such as AIN.
- the upper limit may be 0.05, 0.04, 0.03, 0.02 or 0.015%.
- Nitrogen is restricted to 0.08 % in order to obtain the desired type and amount of hard phases, in particular V(C,N).
- vanadium rich carbonitrides V(C,N) will form. These will be partly dissolved during the austenitizing step and then precipitated during the tempering step as particles of nanometer size.
- the thermal stability of vanadium carbonitrides is considered to be better than that of vanadium carbides, hence the tempering resistance of the tool steel may be improved and the resistance against grain growth at high austenitizing temperatures is enhanced.
- the lower limit may be 0.001, 0.004, 0.01, 0.011, 0.012, 0.013, 0.014, 0.015, 0.016 or 0.017%.
- the upper limit may be 0.07, 0.06, 0.05, 0.04, 0.03 or 0.01 %.
- Hydrogen is known to have a deleterious effect on the properties of the steel and to cause problems during processing.
- the upper limit can be set to 0.0004% (4 ppm) and it may be limited to 3, 2.5, 2, 1.5 or 1 ppm.
- Nickel may be present in an amount of ⁇ 1.5 %. It gives the steel a good hardenability and toughness. However, because of the expense, the nickel content of the steel should be limited.
- the upper limit may therefore be set to 1.0, 0.8, 0.5 or 0.3%.
- the lower limit may be set to 0.05, 0.10, 0.15 or 0.20 %.
- Cu is an optional element, which may contribute to increasing the hardness and the corrosion resistance of the steel. If used, the preferred range is 0.02 - 1%.
- the lower limit may beset to 0.05, 0.1 or 0.15 %.
- the upper limit may be set to 0.6, 0.4 0.3 or 0.2 %.
- Co is an optional element. Co causes the solidus temperature to increase and therefore provides an opportunity to raises the hardening temperature, which may be 15 - 30 °C higher than without Co. During austenitization it is therefore possible to dissolve larger fraction of carbides and thereby enhance the hardenability. Co also increases the M s temperature.
- the maximum amount is 8 % and, if added, an effective amount may be 2 - 6 %, in particular 4 to 5 %. However, for practical reasons, such as scrap handling, deliberate additions of Co is not made.
- the maximum impurity content may then be set to 1 % or 0.3 %.
- molybdenum may be replaced by twice as much with tungsten because of their chemical similarities.
- tungsten is expensive and it also complicates the handling of scrap metal.
- the maximum amount is therefore limited to 1 %, preferably 0.5 %, more preferably 0.3 % and most preferably no deliberate additions are made.
- Niobium is similar to vanadium in that it forms carbonitrides of the type M(N,C) and may in principle be used to replace part of the vanadium but that requires the double amount of niobium as compared to vanadium.
- Nb results in a more angular shape of the
- M(N,C) The maximum amount is therefore 0.5%, preferably 0.05 % and most preferably no deliberate additions are made.
- These elements are carbide formers and may be present in the alloy in the claimed ranges for altering the composition of the hard phases. However, normally none of these elements are added.
- B may be used in order to further increase the hardness of the steel.
- the amount is limited to 0.01%, preferably ⁇ 0.005%.
- a preferred range for the addition of B is 0.001 - 0.004 %.
- Selenium may be added to the steel in an amount of ⁇ 0.05% in order to further improve the machinability of the steel.
- Y may optionally be added in an amount of up to 1 % in order to improve adherence of the oxide scale and thereby improving the wear resistance of the steel.
- the addition is particularly effective when evenly distributed in the steel matrix.
- Y is therefore preferably added to steels produced by powder metallurgy.
- the lower limit may be set to 0.2, 0.3 or 0.4 %.
- the upper limit may be set to 0.9, 0.8, 0.7 or 0.6 %.
- REM is here defined to consist of the elements 57 to 71 in the periodic table.
- P, S and O are the main impurities, which have a negative effect on the mechanical properties of the steel.
- P may therefore be limited to 0.03%, preferably to 0.01%.
- S may be limited to 0.03, 0.01, 0.00 5, 0.003, 0.001, 0.0008, 0.0005 or even 0.0001%.
- O may be limited to 0.0015, 0.0012, 0.0010, 0.0008, 0.0006 or 0.0005%.
- the invention provides a steel for hot working having a composition consisting of in weight % (wt.%):
- the steel is in an annealed condition, has a hardness of not more than 360 HB and a microstructure comprising:
- the steel should fulfil at least one of the following requirements c 0.30-0.38
- the steel should fulfil at least one of the following requirements
- the steel should fulfil at least one of the following requirements
- the steel should fulfil at least one of the following requirements
- the steel should fulfil the following requirements:
- the packets of the tempered martensite and/or bainite should have a maximum size of 40 ⁇ , preferably 20 ⁇ , more preferably 15 ⁇ .
- the hard phase comprises Me , M7C3, M23C6 and MC, wherein M is one or more metals of Cr, Mo, V and Nb and wherein the hard phase, apart from C, may comprise N and B.
- the amount of hard phase is 3-8 vol. % and/or the maximum size of the hard phase ⁇ 5 3 ⁇ .
- the steel in the annealed condition has a hardness of not more than 300 HB, preferably not more than 250 HB.
- a preferred hardness range is 180-250 HB, preferably 190-230 HB.
- the steel fulfils the machinability value V1000 (HSS) > 35 m/min.
- a method of producing a steel comprising the steps of:
- the method of producing a steel fulfils at least one of the following requirements: the temperature in step c) is 980-1030 °C, the reheating temperature in step e) is A c i-50 °C to Aci-10 °C and the holding time is 4-8 hours.
- the method of producing a steel may further comprise the step of:
- a tool steel having the claimed chemical composition can be produced by conventional metallurgy including melting in an Electric Arc Furnace (EAF) and further refining in a ladle and vacuum treatment.
- ESR Electro Slag Remelting
- the steel is subjected to hardening and tempering before being used e.g. in a mould for die casting.
- Austenitizing may then be performed at an austenitizing temperature (TA) in the range of 1000-1070 °C, preferably about 1000-1030 °C.
- TA austenitizing temperature
- a typical T A is 1025 °C with a holding time of 30 minutes followed by rapid quenching.
- the tempering temperature is chosen according to the hardness requirement and is performed at least twice at 550 - 650 °C for 2 hours (2x2h) followed by cooling in air. This results in a hardness of 44 - 54 HRC.
- HBW10/3000 i.e. a 10 mm diameter tungsten carbide ball indenter and a load of 3000 kgf. Accordingly, in this application HB is the same as HBW10/3000.
- the inventors of the present invention has surprisingly found that if the conventional soft annealing is replaced by an alternate high temperature annealing slightly below the Aci temperature it is possible to improve the machinability of the steel by providing the steel with a completely different microstructure.
- packets of tempered martensite and/or bainite refers to a structure of carbon depleted packets of tempered martensite and/or bainite with carbides distributed in the grain- and sub-grain boundaries as well as to a packet structure of ferrite having most of the carbides distributed in the grain- and sub-grain boundaries.
- a steel was produced by EAF-melting, ladle refining, and vacuum degassing followed by uphill casting.
- the ingots were subjected to forging to the dimension 799x379 mm. Test pieces of were taken for examination.
- the steel had the following composition in weight % (wt.%): C: 0.35, Si: 0.18, Mn: 0.45, Cr: 5.0, Mo 2.3, V: 0.6 and Al:0.01.
- the Aci for this composition is 820 °C.
- the steel sample according to the invention was subjected to annealing at 800 °C, which is slightly below the Aci temperature. This resulted in a hardness value of 213 HB.
- the hardness of the sample subjected to conventional soft annealing above the Aci temperature was 164 HB. The results are shown in Table 1.
- Fig. 1 discloses the microstructure of the inventive steel, Light Optical Microscope (LOM).
- Fig. 2 discloses the microstructure of the comparative steel, which was subjected to conventional soft annealing (LOM). The length of the bar in the lower right corner in Figures 1 and 2 is 20 ⁇ . It can be seen that the inventive steel has a much finer and more homogeneous structure as well as a finer and more uniform carbide distribution than the soft annealed steel. These differences can be more clearly recognized in the pictures taken in the Scanning Electron Microscope (SEM).
- Fig. 3 discloses a SEM picture of the inventive steel consisting of packets of carbon depleted tempered martensite and carbides mainly distributed in the grain- and sub- grain boundaries.
- Fig. 4 discloses the structure of the comparative steel having coarse carbides uniformly distributed in a matrix of polygonal ferrite.
- Machinability was examined by drilling, since this is one of the toughest operations in tool body manufacture.
- the tests were carried out on a MODIG 7000 machining center.
- the steels were subjected to V1000 drilling test. This test gives the cutting speed for a cutting length of 1000 mm.
- the drills used were HSS Wedevag Double-X 05 mm.
- Table 2 discloses the result according to the invention and Table 3 for the comparative steel.
- the results of the drilling tests were used to derive the VIOOO-values for the steels examined.
- the inventive steel had a V1000 value of 40 m/min and the comparative steel a V1000 value of 30 m/min. Accordingly, the inventive steel revealed a remarkable improved machinability in this test.
- a result of this microstructure is that the hardness of the annealed material increases from about 160 HB to e.g. about 210 HB.
- it has surprisingly been found that the new structure give rise to a very much improved machinability.
- the tool steel of the present invention is particular useful in large dies requiring a good hardenability and a good machinability in the unhardened condition.
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Abstract
The invention relates hot work tool steel. The steel comprises the following main components (in wt. %): C 0.27 -0.40, Si 0.10 -0.35, Mn 0.2 -1.0, Cr 4.0 -6.0, Mo 1.0 -3, V 0.4 -0.9, balance optional elements, iron and impurities, wherein the steel in the annealed condition has a microstructure comprising: a) at least 75 vol. % packets of tempered martensite and/or bainite and b) 1-20 vol. % of hard phase including carbides, nitrides and carbo-nitrides.
Description
HOT WORK TOOL STEEL
TECHNICAL FIELD
The invention relates to a hot work tool steel.
BACKGROUND OF THE INVENTION
Vanadium alloyed matrix tool steels have been on market for decades and attained a considerable interest because of the fact that they combine a high wear resistance with an excellent dimensional stability and because they have a good toughness. These steels have a wide range of applications such as for die casting and forging. The steels are generally produced by conventional metallurgy followed by Electro Slag Remelting (ESR). Uddeholm DIEVAR"9 is a high performance chromium-molybdenum-vanadium steel, containing balanced carbon and vanadium contents as described in WO 99/50468 Al. It is a modified H13 premium hot work tool steel, which is machined in the soft annealed delivery condition. The recommended soft annealing is heating to 850 °C in protecting atmosphere for 4 hours to obtain a uniform temperature followed by cooling at a rate of 10 °C/h to 600 °C and then freely in air. This results in a hardness of approximately 160 HB.
Although the known steel has superior properties than other conventionally produced tool steels with respect to heat checking, gross cracking, hot wear and plastic deformation, there is a need for further improvements of its property profile. In particular, it would be beneficial to improve the machinability of the steel in the unhardened condition. DISCLOSURE OF THE INVENTION
The object of the present invention is to provide a hot work tool steel having an improved property profile, i.e. the inventive steel should be superior over the modified H13 tool steel known in the art in at least one respect.
Another object of the present invention is to improve the machinability of the steel in the unhardened condition. In addition, it would be advantageous if the distortion during the hardening and tempering of the tool steel could be reduced in order to further reduce the machining allowances.
The foregoing objects, as well as additional advantages are achieved to a significant measure by providing a hot work tool steel having a composition and a microstructure as set out in the claims.
The invention is defined in the claims. BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 shows the structure of the inventive steel 800 °C/6h according to the Example. The length of the bar in the lower right corner is 20 μιη.
Fig. 2 shows the structure of the comparative subjected to conventional soft annealing according to the Example. The length of the bar in the lower right corner is 20 μιη. Fig. 3 shows the structure of the inventive steel 800 °C/6h according to the Example.
Fig. 4 shows the structure of the comparative subjected to conventional soft annealing according to the Example.
DETAILED DESCRIPTION OF THE INVENTION
The importance of the separate elements and their interaction with each other as well as the limitations of the chemical ingredients of the claimed alloy are briefly explained in the following. All percentages for the chemical composition of the steel are given in weight % (wt. %) throughout the description. The amount of hard phases is given in volume % (vol. %). Upper and lower limits of the individual elements can be freely combined within the limits set out in the claims. Carbon (0.27 - 0.40 %)
is to be present in a minimum content of 0.27 %, preferably at least 0.28, 0.29, 0.30, 0.31, 0.32, 0.33 or 0.34 %. The upper limit for carbon is 0.40% and may be set to 0.39, 0.38, 0.37, 0.36 or 0.35%. Preferred ranges are 0.30 - 0.38 % and 0.33 - 0. 37 %. In any case, the amount of carbon should be controlled such that the amount of primary carbides of the type M23C6, M7C3 and Me in the steel is limited, preferably the steel is free from such primary carbides.
Silicon (0.10 - 1.0 %)
Silicon is commonly used for deoxidation. Si is present in the steel in a dissolved form and may positively influence the machinability. However, Si is a strong ferrite former and increases the
carbon activity and therefore the risk for the formation of undesired carbides, which negatively affect the impact strength. Silicon is also prone to interfacial segregation, which may result in decreased toughness and thermal fatigue resistance. Si is therefore limited to 1.0 %. The upper limit may be 0.9, 0.8, 0.7, 0.6, 0.5, 0.4, 0.35 0.34, 0.32, 0.30, 0.28, 0.26, 0.24 or 0.22%. The lower limit may be 0.12, 0.14, 0.16, 0.18 and 0.20%. Preferred ranges are 0.10 - 0.25 % and 0.15 - 0.24%.
Manganese (0.2 - 1.0 %)
Manganese contributes to improving the hardenability of the steel and together with sulphur manganese contributes to improving the machinability by forming manganese sulphides. Manganese shall therefore be present in a minimum content of 0.2 %, preferably at least 0.3, 0.35, 0.4, 0.45 or 0.5 %. At higher sulphur contents manganese prevents red brittleness in the steel. The steel shall contain maximum 1.0 %, preferably maximum 0.8, 0.7, 0.6, 0.55 or 0.5 %.
Chromium (2.0 - 6.0 %)
Chromium is to be present in a content of at least 2.0 % in order to provide a good
hardenability in larger cross sections during heat treatment. If the chromium content is too high, this may lead to the formation of high-temperature ferrite, which reduces the hot- workability. The lower limit may be 2.0, 2.5, 3.0, 3.5, 4.0, 4.1, 4.2, 4.3, 4.4, 4.5, 4.6, 4.7, 4.8 or 4.9%. The upper limit may be 6.0, 5.8, 5.6, 5.5, 5.4, 5.2 or 5.1 %.
Molybdenum (1.0 - 3.5 %)
Mo is known to have a very favourable effect on the hardenability. Molybdenum is essential for attaining a good secondary hardening response. The minimum content is 1.0 %, and may be set to 1,2, 1.4, 1.6, 1.8, 2.0, 2.1, 2.2, 2.25 or 2.3 %. Molybdenum is a strong carbide forming element and also a strong ferrite former. The maximum content of molybdenum is therefore 3.5 %. Mo may be limited to 3.4, 3.3, 3.2, 3.1, 3.0, 2.9, 2.8, 2.7, 2.6, 2.5, 2.4 or 2.35 %. Vanadium (0.4 - 0.9 %)
Vanadium forms evenly distributed primary precipitated carbides and carbonitrides of the type V(N,C) in the matrix of the steel. This hard phase may also be denoted MX, wherein M is mainly V but Cr and Mo may be present and X is one or more of C, N and B. Vanadium shall therefore be present in an amount of 0.4 - 0.9%. The upper limit may be set to 0.9, 0.8, 0.7, 0.6, 0.58, 0.56 or 0.55 %. The lower limit may be 0.42, 0.44, 0.46, 0.48, 0.50 or 0.52%.
Aluminium (0.001 - 0.06 %)
Aluminium is an optional element and may be used for deoxidation in combination with Si and Mn. The lower limit may be set to 0.001, 0.003, 0.005 or 0.007% in order to ensure a good deoxidation. The upper limit is restricted to 0.06% for avoiding precipitation of undesired phases such as AIN. The upper limit may be 0.05, 0.04, 0.03, 0.02 or 0.015%.
Nitrogen (< 0.08 %)
Nitrogen is restricted to 0.08 % in order to obtain the desired type and amount of hard phases, in particular V(C,N). When the nitrogen content is properly balanced against the vanadium content, vanadium rich carbonitrides V(C,N) will form. These will be partly dissolved during the austenitizing step and then precipitated during the tempering step as particles of nanometer size. The thermal stability of vanadium carbonitrides is considered to be better than that of vanadium carbides, hence the tempering resistance of the tool steel may be improved and the resistance against grain growth at high austenitizing temperatures is enhanced. The lower limit may be 0.001, 0.004, 0.01, 0.011, 0.012, 0.013, 0.014, 0.015, 0.016 or 0.017%. The upper limit may be 0.07, 0.06, 0.05, 0.04, 0.03 or 0.01 %.
Hydrogen (< 0.0004 %)
Hydrogen is known to have a deleterious effect on the properties of the steel and to cause problems during processing. In order to avoid problems related to hydrogen the molten steel is subjected to vacuum degassing. The upper limit can be set to 0.0004% (4 ppm) and it may be limited to 3, 2.5, 2, 1.5 or 1 ppm.
Nickel (<1.5 %)
Nickel may be present in an amount of <1.5 %. It gives the steel a good hardenability and toughness. However, because of the expense, the nickel content of the steel should be limited. The upper limit may therefore be set to 1.0, 0.8, 0.5 or 0.3%. The lower limit may be set to 0.05, 0.10, 0.15 or 0.20 %.
Copper (< 2.0%)
Cu is an optional element, which may contribute to increasing the hardness and the corrosion resistance of the steel. If used, the preferred range is 0.02 - 1%. The lower limit may beset to 0.05, 0.1 or 0.15 %. The upper limit may be set to 0.6, 0.4 0.3 or 0.2 %. However, it is not
possible to extract copper from the steel once it has been added. This drastically makes the scrap handling more difficult. For this reason, copper is normally not deliberately added.
Cobalt (< 8 %)
Co is an optional element. Co causes the solidus temperature to increase and therefore provides an opportunity to raises the hardening temperature, which may be 15 - 30 °C higher than without Co. During austenitization it is therefore possible to dissolve larger fraction of carbides and thereby enhance the hardenability. Co also increases the Ms temperature.
However, large amount of Co may result in a decreased toughness and wear resistance. The maximum amount is 8 % and, if added, an effective amount may be 2 - 6 %, in particular 4 to 5 %. However, for practical reasons, such as scrap handling, deliberate additions of Co is not made. The maximum impurity content may then be set to 1 % or 0.3 %.
Tungsten (< 1 %)
In principle, molybdenum may be replaced by twice as much with tungsten because of their chemical similarities. However, tungsten is expensive and it also complicates the handling of scrap metal. The maximum amount is therefore limited to 1 %, preferably 0.5 %, more preferably 0.3 % and most preferably no deliberate additions are made.
Niobium (< 0.5%)
Niobium is similar to vanadium in that it forms carbonitrides of the type M(N,C) and may in principle be used to replace part of the vanadium but that requires the double amount of niobium as compared to vanadium. However, Nb results in a more angular shape of the
M(N,C). The maximum amount is therefore 0.5%, preferably 0.05 % and most preferably no deliberate additions are made.
Ti, Zr and Ta
These elements are carbide formers and may be present in the alloy in the claimed ranges for altering the composition of the hard phases. However, normally none of these elements are added.
Boron (< 0.01%)
B may be used in order to further increase the hardness of the steel. The amount is limited to 0.01%, preferably < 0.005%. A preferred range for the addition of B is 0.001 - 0.004 %.
Selenium (< 0.05%)
Selenium may be added to the steel in an amount of < 0.05% in order to further improve the machinability of the steel.
Yttrium (< 1 %)
Y may optionally be added in an amount of up to 1 % in order to improve adherence of the oxide scale and thereby improving the wear resistance of the steel. The addition is particularly effective when evenly distributed in the steel matrix. Y is therefore preferably added to steels produced by powder metallurgy. The lower limit may be set to 0.2, 0.3 or 0.4 %. The upper limit may be set to 0.9, 0.8, 0.7 or 0.6 %. Ca, Mg and REM (Rare Earth Metals)
These elements may be added to the steel in the claimed amounts in order to further improve the machinability, hot workability and/or weldability. REM is here defined to consist of the elements 57 to 71 in the periodic table.
Impurity elements
P, S and O are the main impurities, which have a negative effect on the mechanical properties of the steel. P may therefore be limited to 0.03%, preferably to 0.01%. S may be limited to 0.03, 0.01, 0.00 5, 0.003, 0.001, 0.0008, 0.0005 or even 0.0001%. O may be limited to 0.0015, 0.0012, 0.0010, 0.0008, 0.0006 or 0.0005%.
The invention provides a steel for hot working having a composition consisting of in weight % (wt.%):
c 0.27 - 0.40
Si 0.10 - 1.0
Mn 0.2 - 1.0
Cr 2.0 - 6.0
Mo 1.0 - 3.5
V 0.4 - 0.9
optionally one or more of
Al 0.001 - 0.06
N < 0.08
Ni < 1.5
Cu <2
Co <8
W < 1
Nb <0.5
Ti <0.05
Zr <0.05
Ta <0.05
B <0.01
Se <0.05
Ca 0.0001 - 0.009
Mg <0.01
Y < 1
REM <0.2
balance Fe apart from impurities,
wherein the steel is in an annealed condition, has a hardness of not more than 360 HB and a microstructure comprising:
a) at least 75 vol. % packets of tempered martensite and/or bainite, and b) 1-20 vol. % of hard phase including carbides, nitrides and carbo-nitrides.
According to another aspect the steel should fulfil at least one of the following requirements c 0.30-0.38
Si 0.15-0.35
Mn 0.4-0.8
Cr 3.5-5.5
Mo 1.8-2.8
V 0.5-0.6
N 0.001-0.03
Cu 0.02-1
According to another aspect the steel should fulfil at least one of the following requirements
C 0.30-0.38
Si 0.15-0.30
Mn 0.4-0.6
Mo 2.1-2.8
V 0.5-0.6
N 0.001-0.056
According to another aspect the steel should fulfil at least one of the following requirements
C 0.33-0.37
Si 0.16-0.26
Mn 0.45-0.55
Cr 4.8-5.2
Mo 2.2-2.6
V 0.51-0.58
N 0.004 - 0.02
According to another aspect the steel should fulfil at least one of the following requirements
C 0.30-0.38
Si 0.15-0.30
Mn 0.4-0.6
Cr 4.5-5.5
Mo 2.1-2.8
V 0.5-0.6
N <0.01
According to another aspect the steel should fulfil the following requirements:
C 0.33-0.37
Si 0.16-0.26
Mn 0.45-0.55
Cr 4.8-5.2
Mo 2.2-2.6
V 0.51-0.58
According to another aspect the packets of the tempered martensite and/or bainite should have a maximum size of 40 μιη, preferably 20 μιη, more preferably 15 μιη.
According to another aspect the hard phase comprises Me , M7C3, M23C6 and MC, wherein M is one or more metals of Cr, Mo, V and Nb and wherein the hard phase, apart from C, may comprise N and B.
Preferably, the amount of hard phase is 3-8 vol. % and/or the maximum size of the hard phase Ϊ5 3 μιη.
According to another aspect the steel in the annealed condition has a hardness of not more than 300 HB, preferably not more than 250 HB. A preferred hardness range is 180-250 HB, preferably 190-230 HB.
According to another aspect the steel fulfils the machinability value V1000 (HSS) > 35 m/min. A method of producing a steel comprising the steps of:
a) providing a steel having a composition as defined in any of claims 1-6, b) subjecting said steel to hot deformation,
c) subjecting the hot deformed steel to a heat treatment at a temperature in the range of 970 °C to 1050 °C for 2-8 hours in order to austenitize the steel,
d) cooling the steel to a temperature of 70-220 °C in order to obtain a martensitic and/or bainitic structure, and
e) reheating the steel to a temperature of Aci-100 °C to Aci for 2-10 hours.
Preferably the method of producing a steel fulfils at least one of the following requirements: the temperature in step c) is 980-1030 °C, the reheating temperature in step e) is Aci-50 °C to Aci-10 °C and the holding time is 4-8 hours.
The method of producing a steel may further comprise the step of:
f) hardening the steel from a temperature of 980-1080 °C, and
optionally
g) tempering the steel. A tool steel having the claimed chemical composition can be produced by conventional metallurgy including melting in an Electric Arc Furnace (EAF) and further refining in a ladle and vacuum treatment. Optionally the steel may be subjected to Electro Slag Remelting (ESR) in order to further improve the cleanliness and the microstructural homogeneity.
Normally the steel is subjected to hardening and tempering before being used e.g. in a mould for die casting. Austenitizing may then be performed at an austenitizing temperature (TA) in the range of 1000-1070 °C, preferably about 1000-1030 °C. A typical TA is 1025 °C with a holding time of 30 minutes followed by rapid quenching. The tempering temperature is chosen according to the hardness requirement and is performed at least twice at 550 - 650 °C for 2 hours (2x2h) followed by cooling in air. This results in a hardness of 44 - 54 HRC.
However, the steel block used to make a mould or die is machined in the unhardened condition. Although, the prior art steel Uddeholm DIEVAFf has a low hardness of
approximately 160 HB in the soft annealed condition and easily meet NADAC 207-97 requirements of a maximum hardness of 230 HB for premium hot work tool steels, it has a moderate machinability. The hardness test used for all values in this application was
HBW10/3000, i.e. a 10 mm diameter tungsten carbide ball indenter and a load of 3000 kgf. Accordingly, in this application HB is the same as HBW10/3000.
The inventors of the present invention has surprisingly found that if the conventional soft annealing is replaced by an alternate high temperature annealing slightly below the Aci temperature it is possible to improve the machinability of the steel by providing the steel with a completely different microstructure.
The annealing of a martensitic and/or bainitic structure slightly below the Aci temperature results in a redistribution of the carbon and precipitation of carbides. The structure of the lath martensite and/or bainite remains because the material was not subjected to any
transformation into austenite. The carbides are mainly found at the grain and sub-grain boundaries. The precipitation of carbides results in a decrease in tetragonality of the martensite and finally, the packets of lath martensite and/or bainite are transferred into packets of ferrite. Accordingly, term "packets of tempered martensite and/or bainite" refers to a structure of carbon depleted packets of tempered martensite and/or bainite with carbides distributed in the grain- and sub-grain boundaries as well as to a packet structure of ferrite having most of the carbides distributed in the grain- and sub-grain boundaries.
EXAMPLE
In this example a steel was produced by EAF-melting, ladle refining, and vacuum degassing
followed by uphill casting. The ingots were subjected to forging to the dimension 799x379 mm. Test pieces of were taken for examination.
The steel had the following composition in weight % (wt.%): C: 0.35, Si: 0.18, Mn: 0.45, Cr: 5.0, Mo 2.3, V: 0.6 and Al:0.01. The Aci for this composition is 820 °C. The samples were subjected to austenitizing at 990 °C for 4 hours and cooling time of 100 second between 800 and 500 °C (t8/5 = 100s) and thereafter freely in air to 180 °C. The steel sample according to the invention was subjected to annealing at 800 °C, which is slightly below the Aci temperature. This resulted in a hardness value of 213 HB. The hardness of the sample subjected to conventional soft annealing above the Aci temperature was 164 HB. The results are shown in Table 1.
Table 1. Results of the heat treatments
Fig. 1 discloses the microstructure of the inventive steel, Light Optical Microscope (LOM). Fig. 2 discloses the microstructure of the comparative steel, which was subjected to conventional soft annealing (LOM). The length of the bar in the lower right corner in Figures 1 and 2 is 20 μιη. It can be seen that the inventive steel has a much finer and more homogeneous structure as well as a finer and more uniform carbide distribution than the soft annealed steel. These differences can be more clearly recognized in the pictures taken in the Scanning Electron Microscope (SEM). Fig. 3 discloses a SEM picture of the inventive steel consisting of packets of carbon depleted tempered martensite and carbides mainly distributed in the grain- and sub- grain boundaries. Fig. 4 discloses the structure of the comparative steel having coarse carbides uniformly distributed in a matrix of polygonal ferrite.
Machinability was examined by drilling, since this is one of the toughest operations in tool body manufacture. The tests were carried out on a MODIG 7000 machining center.
The steels were subjected to V1000 drilling test. This test gives the cutting speed for a cutting length of 1000 mm. The drills used were HSS Wedevag Double-X 05 mm.
Table 2 discloses the result according to the invention and Table 3 for the comparative steel.
Table 2. Result of the drilling test for the inventive steel. V1000=40 m/min.
Table 3. Result of the drilling test for the comparative steel. V1000=30m/min.
The results of the drilling tests were used to derive the VIOOO-values for the steels examined. The inventive steel had a V1000 value of 40 m/min and the comparative steel a V1000 value of 30 m/min. Accordingly, the inventive steel revealed a remarkable improved machinability in this test. A result of this microstructure is that the hardness of the annealed material increases from about 160 HB to e.g. about 210 HB. In addition thereto, it has surprisingly been found that the new structure give rise to a very much improved machinability.
The reason for the improved machinability is as present not fully understood and the inventors do not want to be bound by any theory. However, one reason for the improved machinability might be that the fine grained structure resulting from the small packet size influences positively on the machinability and offsets the negative effect of an increased hardness. Possibly, the fine grained structure results in smaller chip segments and thereby in lower cutting forces.
INDUSTRIAL APPLICABILITY
The tool steel of the present invention is particular useful in large dies requiring a good hardenability and a good machinability in the unhardened condition.
Claims
1. A steel for hot working having a composition consisting of in weight % (wt.%):
C 0.27 - 0.40
Si 0.10-1.0
Mn 0.2-1.0
Cr 2.0-6.0
Mo 1.0-3.5
V 0.4-0.9
optionally one or more of
Al 0.001-0.06
N <0.08
Ni < 1.5
Cu <2
Co <8
W < 1
Nb <0.5
Ti <0.05
Zr <0.05
Ta <0.05
B <0.01
Se <0.05
Ca 0.0001 - 0.009
Mg <0.01
Y < 1
REM <0.
2
balance Fe apart from impurities,
wherein the steel is in an annealed condition, has a hardness of not more than 360 HB and a microstructure comprising:
a) at least 75 vol. % packets of tempered martensite and/or bainite and b) 1-20 vol. % of hard phase including carbides, nitrides and carbo-nitrides.
A steel according to claim 1 fulfilling at least one of the following requirements: c 0.30-0.38
Si 0.15-0.35
Mn 0.4-0.8
Cr 3.5-5.5
Mo 1.8-2.8
V 0.5-0.6
N 0.001-0.03
H < 0.0003
Cu 0.02-1
Co < 1
W <0.
3
Nb <0.05
Ti <0.01
Zr <0.01
Ta <0.01
B < 0.005
Se <0.03
Mg < 0.001
Y 0.2-1.0
and wherein the impurity contents of P, S and O fulfils the following requirements
P < 0.03
S < 0.03
O < 0.0015
A steel according to claim 1 or 2 fulfilling at least one of the following requirements:
C 0.30-0.38
Si 0.15-0.30
Mn 0.
4-0.6
Cr 4.5-5.5
Mo 2.1-2.8
V 0.
5-0.
6
N 0.001-0.056
H < 0.0002
Cu 0.02-0.5
Co < 1
W <0.3
Nb <0.5
Ti <0.01
Zr <0.01
Ta <0.01
B < 0.005
Se <0.03
Mg < 0.001
Y 0.3-0.
7
and wherein the impurity contents of P, S and O fulfils the following requirements
P <0.01
S < 0.0015
O < 0.0010 A steel according to any of the preceding claims fulfilling at least one of the following requirements:
c 0.33-0.37
Si 0.16-0.26
Mn 0.45 - 0.55
Cr 4.8-5.2
Mo 2.2-2.6
V 0.51-0.58
N 0.004 - 0.02
H < 0.0003
Cu 0.02-0.3
Co <0.3
W <0.1
Nb <0.05
Y 0.4-0.6
and wherein the impurity contents of P, S and O fulfils the following requirements
P <0.01
S < 0.0005
O < 0.0008
A steel according to any of the preceding claims fulfilling the following requirements:
c 0.30-0.38
Si 0.15-0.30
Mn 0.4-0.6
Cr 4.5-5.5
Mo 2.1-2.8
V 0.5-0.6
N <0.01
A steel according to any of the preceding claims fulfilling the following requirements:
C 0.33-0.37
Si 0.16-0.26
Mn 0.45-0.55
Cr 4.
8-5.2
Mo 2.2-2.6
V 0.51-0.58
A steel according to any of the preceding claims, wherein the packets of the tempered martensite and/or bainite have a maximum size of 40 μιη, preferably 20 μιη, more preferably 15 μιη.
A steel according to any of the preceding claims, wherein the hard phase comprises MeC, M7C3, M23C6 and MC, wherein M is one or more metals of Cr, Mo, V and Nb and wherein the hard phases, apart from C, may comprise N and B.
9. A steel according to any of the preceding claims, wherein the amount of hard phase is 3-8 vol. % and/or the maximum size of the hard phase is 3 μιη.
10. A steel according to any of the preceding claims, wherein the steel in the annealed
condition has a hardness of not more than 300 HB, preferably not more than 250 HB.
11. A steel according to any of the preceding claims, wherein the steel in the annealed
condition has a hardness of 180-250 HB, preferably, 190-230 HB.
12. A steel according to claim 10, wherein the steel fulfils the following machinability value V1000 (HSS) > 35 m/min.
13. A method of producing a steel comprising the steps of:
a) providing a steel having a composition as defined in any of claims 1-6, b) subjecting said steel to hot deformation,
c) subjecting the hot deformed steel to a heat treatment at a temperature in the range of 970 °C to 1050 °C for 2-8 hours in order to austenitize the steel,
d) cooling the steel to a temperature of 70-220 °C in order to obtain a martensitic and/or bainitic structure and
e) reheating the steel to a temperature of Aci-100 °C to Aci for 2-10 hours.
14. A method of producing a steel according to claim 13 fulfilling at least one of the following requirements: the temperature in step c) is 980-1030 °C, the reheating temperature in step e) is Aci-50 °C to Aci-10 °C and the holding time is 4-8 hours.
15. A method of producing a steel according to claim 13 or 14 further comprising the step of:
f) hardening the steel from a temperature of 980-1080 °C and
optionally
g) tempering the steel.
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