EP1731625A1 - Steel wire for spring - Google Patents
Steel wire for spring Download PDFInfo
- Publication number
- EP1731625A1 EP1731625A1 EP05709768A EP05709768A EP1731625A1 EP 1731625 A1 EP1731625 A1 EP 1731625A1 EP 05709768 A EP05709768 A EP 05709768A EP 05709768 A EP05709768 A EP 05709768A EP 1731625 A1 EP1731625 A1 EP 1731625A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- steel wire
- spring
- mass
- steel
- impurities
- 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.)
- Granted
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- 229910000831 Steel Inorganic materials 0.000 title claims abstract description 151
- 239000010959 steel Substances 0.000 title claims abstract description 151
- 238000010438 heat treatment Methods 0.000 claims abstract description 42
- 229910000639 Spring steel Inorganic materials 0.000 claims abstract description 40
- 238000005496 tempering Methods 0.000 claims abstract description 29
- 230000009467 reduction Effects 0.000 claims abstract description 25
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 24
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 23
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 22
- 239000012535 impurity Substances 0.000 claims abstract description 21
- 229910052742 iron Inorganic materials 0.000 claims abstract description 21
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 13
- 229910000734 martensite Inorganic materials 0.000 claims abstract description 11
- 229910001566 austenite Inorganic materials 0.000 claims description 23
- 238000000034 method Methods 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 19
- 239000000126 substance Substances 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 13
- 230000008569 process Effects 0.000 claims description 12
- 230000009466 transformation Effects 0.000 claims description 12
- 229910052750 molybdenum Inorganic materials 0.000 claims description 10
- 229910052721 tungsten Inorganic materials 0.000 claims description 10
- 229910052758 niobium Inorganic materials 0.000 claims description 9
- 229910052719 titanium Inorganic materials 0.000 claims description 9
- 229910052720 vanadium Inorganic materials 0.000 claims description 8
- 239000011572 manganese Substances 0.000 description 24
- 239000011651 chromium Substances 0.000 description 20
- 238000005121 nitriding Methods 0.000 description 19
- 239000010936 titanium Substances 0.000 description 16
- 238000010791 quenching Methods 0.000 description 11
- 230000000171 quenching effect Effects 0.000 description 11
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 10
- 239000010955 niobium Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- 238000009472 formulation Methods 0.000 description 7
- 230000005540 biological transmission Effects 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- 230000006872 improvement Effects 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 230000014759 maintenance of location Effects 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000003252 repetitive effect Effects 0.000 description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- 239000010941 cobalt Substances 0.000 description 3
- 229910017052 cobalt Inorganic materials 0.000 description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 238000005491 wire drawing Methods 0.000 description 3
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 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
- 238000003723 Smelting Methods 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 238000000137 annealing Methods 0.000 description 2
- 229910001567 cementite Inorganic materials 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000005242 forging Methods 0.000 description 2
- 238000005098 hot rolling Methods 0.000 description 2
- KSOKAHYVTMZFBJ-UHFFFAOYSA-N iron;methane Chemical compound C.[Fe].[Fe].[Fe] KSOKAHYVTMZFBJ-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000011733 molybdenum Substances 0.000 description 2
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 2
- 239000010937 tungsten Substances 0.000 description 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 2
- 229910020630 Co Ni Inorganic materials 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000010420 art technique Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229910052729 chemical element Inorganic materials 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 230000001010 compromised effect Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000009661 fatigue test Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910001562 pearlite Inorganic materials 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 229910000859 α-Fe 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
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/02—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for springs
-
- 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
- C21D1/19—Hardening; Quenching with or without subsequent tempering by interrupted quenching
- C21D1/20—Isothermal quenching, e.g. bainitic hardening
-
- 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
- C21D1/25—Hardening, combined with annealing between 300 degrees Celsius and 600 degrees Celsius, i.e. heat refining ("Vergüten")
-
- 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
- C21D8/06—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of rods or wires
- C21D8/065—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of rods or wires 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
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/30—Ferrous alloys, e.g. steel alloys containing chromium with cobalt
-
- 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
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/008—Martensite
-
- 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
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/52—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for wires; for strips ; for rods of unlimited length
- C21D9/525—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for wires; for strips ; for rods of unlimited length for wire, for rods
Definitions
- the present invention relates to a spring steel wire having a tempered martensitic structure brought about by quenching-tempering, to a method of manufacturing the spring steel wire in a well-suited efficient manner, and to a spring manufactured from the steel wire. More particularly, the present invention relates to a high toughness spring steel wire having a high strength with excellent fatigue properties that is advantageously applicable to engine valve springs or those springs used for transmission interior parts, etc. of automobiles.
- Patent document 1 Japanese Patent Publication No. 2842579
- springs such as engine valve springs or springs for transmission parts have been increasingly required to have better mechanical or physical properties in recent years, so that further improvement has come to be demanded in spring steel wires and springs worked from the steel wire.
- spring steel wires and springs manufactured therefrom be provided with fatigue properties and toughness in better balance than ever.
- springs worked from steel wires are typically subjected to heat treatment (nitriding treatment) at elevated temperatures (specifically, around 420-480°C).
- the patent document 1 discloses a technique that aims at improving the toughness of a steel wire by providing it with a C (carbon) content ranging from 0.3% to 0.5% by weight.
- a steel wire with a carbon content as low as less than 0.50% by weight will have a reduced thermal resistance
- a spring worked from such a low carbon content steel wire is subjected to nitriding treatment at elevated temperatures as described above, the resultant spring will have a reduced fatigue strength, so that it may undergo internal breakage when put into practical use.
- the patent document 3 discloses a technique that aims at improving a steel wire in its workability into sprang by decarbonizing its surface purposely during the oil tempering so as to reduce the surface hardness, but this prior art technique is inadequate for the mass production of such a steel wire or spring because it is practically difficult to obtain a uniform decarburized layer in the surface of the steel wire. Moreover, the oxygen concentration must be well controlled when heating the steel wire (during the oil tempering), thus adding to the cost accordingly.
- the proof stress of the material (spring) to a stress exerted inside in its torsional direction i.e., the shear yield stress of the spring is not examined subsequent to the nitriding treatment to which the spring is subjected after worked from the steel wire.
- a principal object of the present invention is to provide a high strength spring steel wire which is excellent not only in fatigue strength but also in toughness. Also, it is another object of the present invention to provide a spring manufactured from the above-described steel wire and a suitable method to manufacture the spring steel wire.
- the present invention provides a spring steel wire, in which its reduction of area after quenching-tempering and its shear yield stress after subjected to heat treatment comparable to nitriding treatment following the above quenching-tempering are limited to specific ranges, respectively.
- the present invention provides a spring steel wire which has a tempered martensitic structure brought about by quenching-tempering.
- the present spring steel wire is characterized by a 40% or higher reduction of area and by a 1,000 MPa or higher shear yield stress after subjected to heat treatment for at least 2 hours at a temperature ranging from 420°C to 480°C.
- the spring steel wire preferably comprises any one of the following chemical formulations 1 through 6:
- the present invention also provides a method of manufacturing the above-described spring steel wire in a well suited manner therefor, as will be described herein below. More specifically, the method of manufacturing the spring steel wire according to the present invention comprises patenting a steel having any one of the chemical formulations (A) through (C) given below, drawing the patented steel into a steel wire, and subjecting the resultant steel wire to quenching-tempering.
- the above-mentioned patenting process comprises an austenization step in which the steel is heated at 900-1,050°C for 60 to 180 seconds, and an isothermal transformation step in which the thus austenized steel is heated at 600-750°C for 20 to 100 seconds.
- the improvement of a spring in its fatigue properties may preferably be addressed in terms of the suppression of its fatigue breakage.
- a repetitive stress is exerted on the spring not only in the tensile and compression directions but also in the shear direction simultaneously.
- the spring undergoes a repetitive slip deformation (plastic deformation) locally or intensively and creates projections and depressions in the surface region to induce cracks leading to breakage, namely resulting in fatigue breakage. Therefore, for suppressing the fatigue breakage of the spring, it will be effective to suppress such a local or concentrated plastic deformation.
- the steel wire is typically subjected to heat treatment such as nitriding treatment after worked into spring to increase its surface hardness and thereby to increase its fatigue limit.
- heat treatment such as nitriding treatment after worked into spring to increase its surface hardness and thereby to increase its fatigue limit.
- mere an increase in fatigue limit of the springs may sometimes be insufficient to allow their practical use, because such springs tend to undergo permanent set in fatigue.
- the present invention provides a spring steel wire having a reduction of area limited to a specific range of 40% or higher.
- the steel wire tends to undergo in-process breakage when worked into spring and its mass productivity could be substantially compromised thereby.
- the reduction of area may decrease a little when subjecting the steel wire to such particular heat treatment comparable to nitriding treatment that is accomplished at a temperature ranging from 420°C to 480°C for at least 2 hours following the quenching-tempering as described previously.
- the steel wire has a 40% or higher reduction of area after quenching-tempering as described above, it can maintain a 35% or higher reduction of area even after the above-described heat treatment, and a spring manufactured from this steel wire can have a high fatigue properties.
- the reduction of area of a spring steel wire and its shear yield stress after subjected to heat treatment comparable to nitriding treatment following the above quenching-tempering are limited to specific ranges, respectively, to provide the spring steel wire and the spring manufactured from the steel wire with a high fatigue strength and high toughness in adequate balance.
- the present invention specifically limits the present steel wire to predetermined optimal chemical compositions and optimal manufacturing conditions, especially patenting conditions.
- the fatigue limit of a spring can be improved by increasing the surface hardness of the spring by subjecting it to the heat treatment such as nitriding treatment or like after it is worked from a steel wire
- an internal hardness of the spring decreases by the heat treatment to sometimes cause the spring to undergo internal breakage in use.
- the steel wire to be worked into a spring contains carbon (C) and silicon (Si) in a quantity (in mass %) falling in a predetermined range in order to improve the thermal resistance of a matrix of the steel wire.
- the steel wire contains a predetermined quantity of chromium (Cr) in order to produce carbide in the structure of the steel wire when it is tempered and to thereby increase the softening resistance of the steel wire.
- the steel wire may contain also a predetermined quantity of molybdenum (Mo), vanadium (V), niobium (Nb), Tungsten (W), or titanium (Ti) to effectively increase the softening resistance.
- Mo molybdenum
- V vanadium
- Nb niobium
- W Tungsten
- Ti titanium
- the inventors have found out that, for improving the shear yield stresses of the steel wire and the spring manufactured therefrom of the present invention, it is effective to provide the steel wire with a 0.02-1.00 mass % cobalt (Co) content or a rather excess manganese (Mn) content (over 0.7 to 1.5 mass %).
- the steel wire of the present invention has Mn and Co contents limited to specific ranges, respectively. The ranges of these contents and the grounds for such limitation will be described in detail herein later.
- the spring steel wire of the present invention is obtained by subjecting a steel having the above-described chemical compositions to the following processes in sequence: steel ingot making ⁇ hot forging ⁇ hot rolling ⁇ patenting ⁇ wire drawing ⁇ quenching-tempering
- a steel rod is subjected, before wire drawing, to patenting under particular conditions to fully austenitize the structure of the steel to thereby dissolve the undissolved carbide and to obtain a homogeneous pearlitic structure through an appropriate isothermal transformation following the austenitization. Insufficient austenitization may cause the reduction of toughness and shear yield stress of the resultant steel wire. Then, for fully austenitizing the steel, it is preferred to heat the steel rod at a temperature of 900-1,050°C for 60 to 180 seconds.
- the heating temperature is lower than 900°C, or if the heating temperature falls in the range of 900-1,050°C but the heating time is shorter than 60 seconds, sufficient austenitization will not be achieved and undissolved carbide will remain. However, if the heating temperature is higher than 1,050°C, or if the heating temperature falls in the range of 900-1,050°C but the heating time is longer than 180 seconds, austenite grains will become coarse, thus tending to produce martensite during the succeeding transformation, so that the drawability of the steel rod will not be secured during the wire drawing process.
- the steel rod For the isothermal transformation of the steel following the austenitization, it is preferred to heat the steel rod at 600-750°C for 20 to 100 seconds. If the heating temperature is higher than 750°C, or if the heating temperature falls in the 600-750°C range but the heating time is longer than 100 seconds, cementite spheroidizes in the structure of the steel, which may degrade the drawability of the steel rod. On the other hand, if the heating temperature is lower than 600°C, or if the heating temperature falls in the 600-750°C range but the heating time is shorter than 20 seconds, the transformation to pearlite will not be completed and martensite will be produced to thereby degrade the drawability.
- the steel wire obtained by drawing the steel rod which is subjected to patenting as above is then subjected to quenching at too low a temperature, undissolved carbide will remain in the structure of the steel wire, which acts to reduce the toughness of the steel wire.
- the quenching temperature is too high, the austenite grains will grow to larger sizes and consequently the fatigue limits of the steel wire and the spring manufactured therefrom will be reduced.
- the quenching temperature be higher than 850°C but lower than 1,050°C.
- the spring steel wire has a tempered martensitic structure. Moreover, if the austenite grains (prior austenite grains) of the steel wire are rendered fine as observed after subjected to the quenching-tempering, such a steel wire and the spring manufactured from the steel wire will become hard to undergo a slip deformation locally or intensively even when a repetitive stress is applied thereto. That is to say, since the shear yield stress of the steel wire or spring can be improved by rendering fine the austenite grains (prior austenite grains), this consequently contributes to improved fatigue properties of the steel wire or spring.
- the average grain size of the austenite grains fall in the range of 3.0-7.0 micrometers.
- the average grain size can be changed by varying the temperature for patenting the steel rod. More specifically, if the austenitization during patenting is effected at a lower temperature, the grain size will tend to become smaller, while if this austenitizing temperature is increased, the grain size tends to increase. With an average grain size smaller than 3.0 micrometers, undissolved carbide will remain due to the lower austenitizing temperature and tend to reduce the toughness of the steel wire. Meanwhile, if the average grain size is larger than 7.0 micrometers, it is difficult to improve the fatigue limit of the steel wire or the spring manufactured therefrom. Now it is to be noted that the average grain size herein is given in measurements taken on steel wires after drawing and then subjected to quenching-tempering.
- Carbon (C) is an important element which determines the strength of steel, and since a carbon content lower than 0.50 mass % of the total steel will not allow a resulting steel wire to have a sufficient strength, while a carbon content exceeding 0.75 mass % will result in reduced toughness, it is preferred that the carbon content ranges from 0.50 mass % to 0.75 mass %.
- Silicon (Si) is used as a deoxidizer when melting and smelting a raw steel. Moreover, Si is solid-dissolved in steel's ferrite to improve the thermal resistance of the steel and has the effect of preventing the hardness reduction inside the steel wire (spring) due to heat treatment such as strain relief annealing or nitriding treatment to which the spring is subjected after worked from the steel wire. It is preferred that the steel have a Si content ranging from 1.80 mass % to 2.70 mass %, because the 1.80 mass % or higher Si content is required to maintain an adequate thermal resistance but the toughness will decrease if the Si content exceeds 2.70 mass %.
- Mn manganese
- the Mn content required for such a deoxidizer has a lower limit of 0.1 mass %.
- Mn has the effect of improving the hardenability of the steel wire to thereby increase its strength and improve the shear yield stress of the steel wire and the spring manufactured therefrom.
- the Mn content preferably has an upper limit of 1.5 mass %.
- the Mn content may fall in a rather lower range of 0.1-0.7 mass %, while it is preferred for a formulation without Co content that the Mn content fall in a rather higher range of over 0.7 to 1.5 mass %.
- a formulation having a rather higher Mn content may contain also Co.
- a small quantity of cobalt (Co) added to a steel acts to improve the shear yield stress of the resultant steel wire and the spring worked from the steel wire. Also, Co is effective for improving the thermal resistance of the steel wire and for the softening prevention of the spring worked from the steel wire and subjected to the tempering and nitriding treatment. Further, Co does not act to reduce the toughness of the steel wire, so long as its content is low. A Co content lower than 0.02 mass % is hard to contribute to any improved shear yield stress for the steel wire or the spring as described above or to any improved thermal resistance for the steel wire.
- the Co content fall in the range of 0.02 mass % to 1.00 mass %.
- Mn content of the steel may fall in a rather low range of 0.1-0.7 mass %, as described above.
- These elements act to produce carbide in the structure of a steel wire when it is tempered and have the effect of tending to increase the softening resistance of the steel wire. If the content of each of molybdenum (Mo), vanadium (V), tungsten (W) or niobium (Nb) is lower than 0.05 mass % of the total steel, the above-described effect will be hard to achieve. Meanwhile, if the Mo content exceeds 0.50 mass %, if the V content exceeds 0.50 mass %, if the W content exceeds 0.15 mass %, or if the Nb content exceeds 0.15 mass %, the resultant steel wire tends to have reduced toughness in either case.
- Mo molybdenum
- V vanadium
- W tungsten
- Nb niobium
- Titanium acts to produce carbide when the steel wire is tempered and has the effect of tending to increase a softening resistance of the steel wire.
- a Ti content lower than 0.01 mass % will not yield the above-mentioned effect, while a Ti content higher than 0.20 mass % will produce a high-melting point non-metallic inclusion TiO in the structure of the steel wire, tending to reduce the toughness of the steel wire.
- the Ti content preferably ranges from 0.01 mass % to 0.20 mass %.
- the spring steel wire of the present invention may have any cross-sectional shape as cut by a plane perpendicular to the longitudinal direction (drawing direction) of the steel wire, including a typical circular shape and other special or peculiar cross-sectional shapes such as an ellipse, a trapezoid, a square, a rectangle, and so on.
- the spring of the present invention may be provided by subjecting the above-described spring.steel wire to any known spring forming process such as coiling. Especially, it is to be noted here that by subjecting the spring worked from the present spring steel wire to heat treatment such as nitriding treatment or like, the resultant spring can have an improved surface hardness and thus an excellent fatigue limit.
- the respective 6.5 mm ⁇ wire rods were patented under several varied patenting conditions, including austenitizing conditions under which the wire rods were heated at varied temperatures for varied retention times, and conditions for isothermal transformation under which the wire rods were heated also at varied temperatures for varied retention times-subsequentiy to the austenization, as shown in Table 2.
- the resultant steel wires (3.0mm ⁇ ) were then subjected to quenching-tempering.
- quenching the conditions shown in Table 3 were used, while the tempering was carried out using a heating temperature of 450-530°C for all wires.
- the reduction of area (RA) and the average grain sizes (average ⁇ grain size) of austenite grains (prior austenite grains) were measured on the respective quench-tempered wires.
- the results are shown in Table 3.
- the wire quenching temperature was varied to change the average grain size of austenite grains (prior austenite grains).
- the average grain size of austenite grains was determined based on the intercept method subject to JIS G 0522.
- shear yield stress and the fatigue properties were measured on those steel wires which were subjected, after the quenching-tempering, to heat treatment (420°C for 2 hours or 480°C for 2 hours) comparable to nitriding treatment.
- the results are shown also in Table 3.
- the shear yield stress of the steel wires which were heat-treated as above was determined from torque- ⁇ curves obtained through twisting tests on samples of 100d in length (d: sample diameter).
- the fatigue limit was evaluated based on a Nakamura-type rotating bending fatigue test.
- the samples No. 1-4, 6, and 8 having a low shear yield stress after the heat treatment comparable to nitriding treatment turned out to have a low fatigue limit.
- the samples No.2 and 4 had also an inferior toughness with a low reduction of area.
- the steel wires of the samples No. 5 and 7 underwent martensite generation in their wire rod structures during patenting and then frequent wire breakage in the succeeding shaving step, and thus the experiment was forced to stop continuing.
- the sample No. 11 since it had a higher V content of the total steel in addition to its low shear yield stress after the heat treatment, it had a lowered reduction of area of the steel wire to thus reduce its fatigue limit.
- the sample No. 12 since it had a higher Ti content in addition to its low shear yield stress after the heat treatment, it underwent a reduction in fatigue limit owing to breakage caused by Ti-based inclusions.
- the sample No. 9 since it had a smaller average grain size of the austenite grains (prior austenite grains) in addition to its low shear yield stress after the heat treatment, it showed also a low reduction of area.
- the sample No. 10 showed a reduction in fatigue limit, because it had a large average grain size of the austenite grains (prior austenite grains) in addition to its low shear yield stress after the heat treatment.
- the spring steel wire of the present invention is excellent both in fatigue properties and in toughness, it is best suited as a material for springs that are used for parts requiring an adequate fatigue strength.
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Abstract
Description
- The present invention relates to a spring steel wire having a tempered martensitic structure brought about by quenching-tempering, to a method of manufacturing the spring steel wire in a well-suited efficient manner, and to a spring manufactured from the steel wire. More particularly, the present invention relates to a high toughness spring steel wire having a high strength with excellent fatigue properties that is advantageously applicable to engine valve springs or those springs used for transmission interior parts, etc. of automobiles.
- In recent years, as momentum toward low fuel consumption increases in automobiles, the industry has made continued efforts to achieve a further reduction in size and weight of automobile parts, including parts of their engines and transmissions. In connection with this, springs including engine valve springs, springs for transmission parts, etc. have come to be exposed to increasingly severer stress environments year after year, and thus spring materials used therefor are also required to be provided with much more improved fatigue properties accordingly. Heretofore, to manufacture those engine valve springs or springs for transmission parts as described above, it has been known to use silicon-based oil tempered steel wires such as, for example, those described in the patent documents 1-3 listed below.
- [Patent document 1]
Japanese Patent Publication No. 2842579 - [Patent document 2]
Japanese Provisional Patent Publication No. 2002-194496 - [Patent document 3]
Japanese Patent Publication No. 3045795 - However, springs such as engine valve springs or springs for transmission parts have been increasingly required to have better mechanical or physical properties in recent years, so that further improvement has come to be demanded in spring steel wires and springs worked from the steel wire. Especially, it is desired that such spring steel wires and springs manufactured therefrom be provided with fatigue properties and toughness in better balance than ever.
- On the other hand, as improvement in fatigue strength (fatigue limit) is requested recently, springs worked from steel wires are typically subjected to heat treatment (nitriding treatment) at elevated temperatures (specifically, around 420-480°C).
- The patent document 1 discloses a technique that aims at improving the toughness of a steel wire by providing it with a C (carbon) content ranging from 0.3% to 0.5% by weight. However, since a steel wire with a carbon content as low as less than 0.50% by weight will have a reduced thermal resistance, if a spring worked from such a low carbon content steel wire is subjected to nitriding treatment at elevated temperatures as described above, the resultant spring will have a reduced fatigue strength, so that it may undergo internal breakage when put into practical use.
- The patent document 2 discloses a technique that aims at improving the fatigue strength of a steel wire by achieving a fine structure having an average grain size of 1.0-7.0 micrometers as austenite after quenching. However, if the quenching temperature is lowered to make the austenite grain size smaller, there will remain undissolved carbide, which may lower the toughness of the resultant steel wire. Further, with such reduction in toughness, the steel wire will become more susceptible to breakage while being worked into spring and consequently the mass productivity of the spring therefrom will be adversely affected thereby.
- The patent document 3 discloses a technique that aims at improving a steel wire in its workability into sprang by decarbonizing its surface purposely during the oil tempering so as to reduce the surface hardness, but this prior art technique is inadequate for the mass production of such a steel wire or spring because it is practically difficult to obtain a uniform decarburized layer in the surface of the steel wire. Moreover, the oxygen concentration must be well controlled when heating the steel wire (during the oil tempering), thus adding to the cost accordingly.
- Further, in any of the technologies disclosed in the above-cited prior art documents, the proof stress of the material (spring) to a stress exerted inside in its torsional direction, i.e., the shear yield stress of the spring is not examined subsequent to the nitriding treatment to which the spring is subjected after worked from the steel wire.
- Accordingly, a principal object of the present invention is to provide a high strength spring steel wire which is excellent not only in fatigue strength but also in toughness. Also, it is another object of the present invention to provide a spring manufactured from the above-described steel wire and a suitable method to manufacture the spring steel wire.
- With the aforementioned objects in view, the present invention provides a spring steel wire, in which its reduction of area after quenching-tempering and its shear yield stress after subjected to heat treatment comparable to nitriding treatment following the above quenching-tempering are limited to specific ranges, respectively.
- That is, the present invention provides a spring steel wire which has a tempered martensitic structure brought about by quenching-tempering. The present spring steel wire is characterized by a 40% or higher reduction of area and by a 1,000 MPa or higher shear yield stress after subjected to heat treatment for at least 2 hours at a temperature ranging from 420°C to 480°C.
- According to the present invention, the spring steel wire preferably comprises any one of the following chemical formulations 1 through 6:
- 1. Based on mass %; C: 0.50-0.75%, Si: 1.80-2.70%, Mn: 0.1-0.7%, Cr: 0.70-1.50%, Co: 0.02-1.00%, and remnants consisting of Fe and impurities
- 2. Based on mass %; C: 0.50-0.75%, Si: 1.80-2.70%, Mn: over 0.7-1.5%, Cr: 0.70-1.50%, and remnants consisting of Fe and impurities
- 3. Based on mass %; C: 0.50-0.75%, Si: 1.80-2.70%, Mn: over 0.7-1.5%, Cr: 0.70-1.50%, at least one element of Ni: 0.1-1.0% and Co: 0.02-1.00%, and remnants consisting of Fe and impurities
- 4. Based on mass %; C: 0.50-0.75%, Si: 1.80-2.70%, Mn: 0.1-0.7%, Cr: 0.70-1.50%, Co: 0.02-1.00%, at least one element selected from the group of 5 elements consisting of V: 0.05-0.50%, Mo: 0.05-0.50%, W: 0.05-0.15%, Nb: 0.05-0.15% and Ti: 0.01-0.20%, and remnants consisting of Fe and impurities
- 5. Based on mass %;'C: 0.50-0.75%, Si: 1.80-2.70%, Mn: over 0.7-1.5%, Cr: 0.70-1.50%, at least one element selected from the group of 5 elements consisting of V: 0.05-0.50%, Mo: 0.05-0.50%, W: 0.05-0.15%, Nb: 0.05-0.15% and Ti: 0.01-0.20%, and remnant consisting of Fe and impurities
- 6. Based on mass %; C: 0.50-0.75%, Si: 1.80-2.70%, Mn: over 0.7-1.5%, Cr: 0.70-1.50%, at least one element of Ni: 0.1-1.0% and Co: 0.02-1.00%, at least one element selected from the group of 5 elements consisting of V: 0.05-0.50%, Mo: 0.05-0.50%, W: 0.05-0.15%, Nb: 0.05-0.15% and Ti: 0.01-0.20%, and remnant consisting of Fe and impurities
- The present invention also provides a method of manufacturing the above-described spring steel wire in a well suited manner therefor, as will be described herein below. More specifically, the method of manufacturing the spring steel wire according to the present invention comprises patenting a steel having any one of the chemical formulations (A) through (C) given below, drawing the patented steel into a steel wire, and subjecting the resultant steel wire to quenching-tempering. The above-mentioned patenting process comprises an austenization step in which the steel is heated at 900-1,050°C for 60 to 180 seconds, and an isothermal transformation step in which the thus austenized steel is heated at 600-750°C for 20 to 100 seconds.
- (A) Based on mass %; C: 0.50-0.75%, Si: 1.80-2.70%, Mn: 0.1-0.7%, Cr: 0.70-1.50%, Co: 0.02-1.00%, and remnants consisting of Fe and impurities
- (B) Based on mass %; C: 0.50-0.75%, Si: 1.80-2.70%, Mn: over 0.7-1.5%, Cr: 0.70-1.50%, and remnants consisting of Fe and impurities
- (C) Based on mass %; C: 0.50-0.75%, Si: 1.80-2.70%, Mn: over 0.7-1.5%, Cr: 0.70-1.50%, at least one element of Ni: 0.1-1.0% and Co: 0.02-1.00%, and remnants consisting of Fe and impurities
- The improvement of a spring in its fatigue properties may preferably be addressed in terms of the suppression of its fatigue breakage. When a spring is operated repeatedly, a repetitive stress is exerted on the spring not only in the tensile and compression directions but also in the shear direction simultaneously. Thus, with the repetitive stress applied externally, the spring undergoes a repetitive slip deformation (plastic deformation) locally or intensively and creates projections and depressions in the surface region to induce cracks leading to breakage, namely resulting in fatigue breakage. Therefore, for suppressing the fatigue breakage of the spring, it will be effective to suppress such a local or concentrated plastic deformation. Heretofore, in order to suppress such a plastic deformation, the steel wire is typically subjected to heat treatment such as nitriding treatment after worked into spring to increase its surface hardness and thereby to increase its fatigue limit. However, nowadays, when springs have come to be used under conditions where a large stress is applied thereto, mere an increase in fatigue limit of the springs may sometimes be insufficient to allow their practical use, because such springs tend to undergo permanent set in fatigue. This may be accounted by the fact that even if a high hardness nitrided layer at the spring surface formed by the above-mentioned heat treatment such as nitriding treatment or like does not undergo permanent set in fatigue, such a large stress can reduce the strength of the inner part of the spring so as to put springs into permanent set in fatigue. Therefore, for springs, it is desired that springs are improved not only in their fatigue limit but in their torsional proof stress, i.e., shear yield stress itself, in addition to having a high strength. Under these circumstances, the inventors have studied above-described subject from various aspects to find out that an adequate torsional proof stress provided inside the material (i.e., spring) after the above-mentioned heat treatment such as nitriding treatment or like is substantially effective for meeting these requirements. More specifically, it turned out that the fatigue properties of a spring can be improved, if the spring has a 1,000 MPa or higher shear yield stress after the above-mentioned heat treatment such as nitriding treatment or like. Based on these findings, the present invention provides a spring steel wire having a shear yield stress limited to a specific range of 1,000 MPa or higher after subjected to particular heat treatment following the quenching-tempering.
- However high the strength of a steel wire may be, it will undergo in-process breakage when the steel wire is worked into a spring if toughness of the steel wire is insufficient. Consequently the mass productivity of the spring will be hampered. Further, as the toughness of a steel wire used as material for a spring decreases, the fatigue properties of the spring will also decrease. Under these circumstances, the inventors have studied this problem from various aspects to find out that providing the steel wire with a 40% or higher reduction of area after quenching-tempering is effective for the prevention of in-process breakage of the steel wire when worked into spring and thus leads to excellent mass productivity of the spring. Based on these findings, the present invention provides a spring steel wire having a reduction of area limited to a specific range of 40% or higher. With a reduction of area lower than 40%, the steel wire tends to undergo in-process breakage when worked into spring and its mass productivity could be substantially compromised thereby. In this regard, the reduction of area may decrease a little when subjecting the steel wire to such particular heat treatment comparable to nitriding treatment that is accomplished at a temperature ranging from 420°C to 480°C for at least 2 hours following the quenching-tempering as described previously. However, if the steel wire has a 40% or higher reduction of area after quenching-tempering as described above, it can maintain a 35% or higher reduction of area even after the above-described heat treatment, and a spring manufactured from this steel wire can have a high fatigue properties.
- Thus, according to the present invention, the reduction of area of a spring steel wire and its shear yield stress after subjected to heat treatment comparable to nitriding treatment following the above quenching-tempering are limited to specific ranges, respectively, to provide the spring steel wire and the spring manufactured from the steel wire with a high fatigue strength and high toughness in adequate balance.
- In order to provide such a spring steel wire and a spring that are excellent both in fatigue properties and in toughness as described above, the present invention specifically limits the present steel wire to predetermined optimal chemical compositions and optimal manufacturing conditions, especially patenting conditions.
- First, while the fatigue limit of a spring can be improved by increasing the surface hardness of the spring by subjecting it to the heat treatment such as nitriding treatment or like after it is worked from a steel wire, an internal hardness of the spring decreases by the heat treatment to sometimes cause the spring to undergo internal breakage in use. Thus, according to the present invention, the steel wire to be worked into a spring contains carbon (C) and silicon (Si) in a quantity (in mass %) falling in a predetermined range in order to improve the thermal resistance of a matrix of the steel wire. Besides, the steel wire contains a predetermined quantity of chromium (Cr) in order to produce carbide in the structure of the steel wire when it is tempered and to thereby increase the softening resistance of the steel wire. In addition to this predetermined Cr content, the steel wire may contain also a predetermined quantity of molybdenum (Mo), vanadium (V), niobium (Nb), Tungsten (W), or titanium (Ti) to effectively increase the softening resistance. Then the inventors have found out that, for improving the shear yield stresses of the steel wire and the spring manufactured therefrom of the present invention, it is effective to provide the steel wire with a 0.02-1.00 mass % cobalt (Co) content or a rather excess manganese (Mn) content (over 0.7 to 1.5 mass %).
Thus, the steel wire of the present invention has Mn and Co contents limited to specific ranges, respectively. The ranges of these contents and the grounds for such limitation will be described in detail herein later. - The spring steel wire of the present invention is obtained by subjecting a steel having the above-described chemical compositions to the following processes in sequence: steel ingot making → hot forging → hot rolling → patenting → wire drawing → quenching-tempering
- According to the present invention, a steel rod is subjected, before wire drawing, to patenting under particular conditions to fully austenitize the structure of the steel to thereby dissolve the undissolved carbide and to obtain a homogeneous pearlitic structure through an appropriate isothermal transformation following the austenitization.
Insufficient austenitization may cause the reduction of toughness and shear yield stress of the resultant steel wire. Then, for fully austenitizing the steel, it is preferred to heat the steel rod at a temperature of 900-1,050°C for 60 to 180 seconds. If the heating temperature is lower than 900°C, or if the heating temperature falls in the range of 900-1,050°C but the heating time is shorter than 60 seconds, sufficient austenitization will not be achieved and undissolved carbide will remain. However, if the heating temperature is higher than 1,050°C, or if the heating temperature falls in the range of 900-1,050°C but the heating time is longer than 180 seconds, austenite grains will become coarse, thus tending to produce martensite during the succeeding transformation, so that the drawability of the steel rod will not be secured during the wire drawing process. - For the isothermal transformation of the steel following the austenitization, it is preferred to heat the steel rod at 600-750°C for 20 to 100 seconds. If the heating temperature is higher than 750°C, or if the heating temperature falls in the 600-750°C range but the heating time is longer than 100 seconds, cementite spheroidizes in the structure of the steel, which may degrade the drawability of the steel rod. On the other hand, if the heating temperature is lower than 600°C, or if the heating temperature falls in the 600-750°C range but the heating time is shorter than 20 seconds, the transformation to pearlite will not be completed and martensite will be produced to thereby degrade the drawability.
- If the steel wire obtained by drawing the steel rod which is subjected to patenting as above is then subjected to quenching at too low a temperature, undissolved carbide will remain in the structure of the steel wire, which acts to reduce the toughness of the steel wire. On the contrary, if the quenching temperature is too high, the austenite grains will grow to larger sizes and consequently the fatigue limits of the steel wire and the spring manufactured therefrom will be reduced. Thus, it is preferred that the quenching temperature be higher than 850°C but lower than 1,050°C.
- According to the present invention, the spring steel wire has a tempered martensitic structure. Moreover, if the austenite grains (prior austenite grains) of the steel wire are rendered fine as observed after subjected to the quenching-tempering, such a steel wire and the spring manufactured from the steel wire will become hard to undergo a slip deformation locally or intensively even when a repetitive stress is applied thereto. That is to say, since the shear yield stress of the steel wire or spring can be improved by rendering fine the austenite grains (prior austenite grains), this consequently contributes to improved fatigue properties of the steel wire or spring.
- Specifically, it is preferred that the average grain size of the austenite grains (prior austenite grains) fall in the range of 3.0-7.0 micrometers. The average grain size can be changed by varying the temperature for patenting the steel rod. More specifically, if the austenitization during patenting is effected at a lower temperature, the grain size will tend to become smaller, while if this austenitizing temperature is increased, the grain size tends to increase. With an average grain size smaller than 3.0 micrometers, undissolved carbide will remain due to the lower austenitizing temperature and tend to reduce the toughness of the steel wire. Meanwhile, if the average grain size is larger than 7.0 micrometers, it is difficult to improve the fatigue limit of the steel wire or the spring manufactured therefrom. Now it is to be noted that the average grain size herein is given in measurements taken on steel wires after drawing and then subjected to quenching-tempering.
- Hereinafter, the description will be made on the grounds on which the elements are selected and their contents are limited to specific ranges according to the present invention. In the description to follow, numerical values accompanying the individual elements are all given in mass %.
- Carbon (C) is an important element which determines the strength of steel, and since a carbon content lower than 0.50 mass % of the total steel will not allow a resulting steel wire to have a sufficient strength, while a carbon content exceeding 0.75 mass % will result in reduced toughness, it is preferred that the carbon content ranges from 0.50 mass % to 0.75 mass %.
- Silicon (Si) is used as a deoxidizer when melting and smelting a raw steel. Moreover, Si is solid-dissolved in steel's ferrite to improve the thermal resistance of the steel and has the effect of preventing the hardness reduction inside the steel wire (spring) due to heat treatment such as strain relief annealing or nitriding treatment to which the spring is subjected after worked from the steel wire. It is preferred that the steel have a Si content ranging from 1.80 mass % to 2.70 mass %, because the 1.80 mass % or higher Si content is required to maintain an adequate thermal resistance but the toughness will decrease if the Si content exceeds 2.70 mass %.
- Like Si, manganese (Mn) is used as a deoxidizer when melting and smelting a raw steel. Therefore, it is preferred that the Mn content required for such a deoxidizer has a lower limit of 0.1 mass %. Moreover, Mn has the effect of improving the hardenability of the steel wire to thereby increase its strength and improve the shear yield stress of the steel wire and the spring manufactured therefrom. However, since an Mn content higher than 1.5 mass % of the total steel tends to produce martensite in the steel during the patenting process and thus wire breakage may be caused thereby in the drawing process, the Mn content preferably has an upper limit of 1.5 mass %. Particularly, in cases where the steel contains cobalt (Co) to be described herein below, the Mn content may fall in a rather lower range of 0.1-0.7 mass %, while it is preferred for a formulation without Co content that the Mn content fall in a rather higher range of over 0.7 to 1.5 mass %. A formulation having a rather higher Mn content may contain also Co.
- Since chromium (Cr) acts to improve the hardenability and thus the softening resistance of the steel, it is effective for preventing the spring worked from the steel wire from softening when subjected to heat treatment such as tempering and nitriding treatment. Since a Cr content lower than 0.70 mass % of the total steel will not work to provide a sufficient effect of preventing the softening, preferably the Cr content is 0.70 mass % or higher, while a Cr content exceeding 1.50 mass % will tend to produce martensite during the patenting process to thus cause wire breakage in the drawing process and further to reduce the toughness of the patented (oil-tempered) steel. Therefore, the Cr content preferably falls in the range of 0.70 to 1.50 mass %.
- A small quantity of cobalt (Co) added to a steel acts to improve the shear yield stress of the resultant steel wire and the spring worked from the steel wire. Also, Co is effective for improving the thermal resistance of the steel wire and for the softening prevention of the spring worked from the steel wire and subjected to the tempering and nitriding treatment. Further, Co does not act to reduce the toughness of the steel wire, so long as its content is low. A Co content lower than 0.02 mass % is hard to contribute to any improved shear yield stress for the steel wire or the spring as described above or to any improved thermal resistance for the steel wire. Also, even if the Co content exceeds 1.00 mass %, no significant improvement in effect can be observed over cases with a 1.00 mass % or lower Co content but it just adds to the manufacturing cost of the steel wire or spring. Accordingly, it is preferred that the Co content fall in the range of 0.02 mass % to 1.00 mass %. In addition, where the steel contains Co, Mn content of the steel may fall in a rather low range of 0.1-0.7 mass %, as described above.
- Nickel (Ni) contained in the steel has the effect of improving the corrosion resistance and toughness of the resultant steel wire. An Ni content lower than 0.1 mass % is hard to contribute to any improved properties of the steel wire as mentioned above, and even if the Ni content exceeds 1.0 mass %, no further improvement in the toughness of the resultant steel wire cannot be achieved, but it just adds to its manufacturing cost. Thus, the Ni content preferably ranges from 0.1 mass % to 1.0 mass %.
- These elements act to produce carbide in the structure of a steel wire when it is tempered and have the effect of tending to increase the softening resistance of the steel wire. If the content of each of molybdenum (Mo), vanadium (V), tungsten (W) or niobium (Nb) is lower than 0.05 mass % of the total steel, the above-described effect will be hard to achieve. Meanwhile, if the Mo content exceeds 0.50 mass %, if the V content exceeds 0.50 mass %, if the W content exceeds 0.15 mass %, or if the Nb content exceeds 0.15 mass %, the resultant steel wire tends to have reduced toughness in either case.
- Titanium (Ti) acts to produce carbide when the steel wire is tempered and has the effect of tending to increase a softening resistance of the steel wire. A Ti content lower than 0.01 mass % will not yield the above-mentioned effect, while a Ti content higher than 0.20 mass % will produce a high-melting point non-metallic inclusion TiO in the structure of the steel wire, tending to reduce the toughness of the steel wire. Thus, the Ti content preferably ranges from 0.01 mass % to 0.20 mass %.
- The spring steel wire of the present invention may have any cross-sectional shape as cut by a plane perpendicular to the longitudinal direction (drawing direction) of the steel wire, including a typical circular shape and other special or peculiar cross-sectional shapes such as an ellipse, a trapezoid, a square, a rectangle, and so on.
- The spring of the present invention may be provided by subjecting the above-described spring.steel wire to any known spring forming process such as coiling. Especially, it is to be noted here that by subjecting the spring worked from the present spring steel wire to heat treatment such as nitriding treatment or like, the resultant spring can have an improved surface hardness and thus an excellent fatigue limit.
- Preferred embodiments of the present invention are demonstrated hereinafter. A steel of each formulation containing chemical elements given in Table 1 with remnants consisting of Fe and impurities were melted in a vacuum melting furnace to prepare an ingot and then the resultant ingot was worked through hot forging and hot rolling into a wire rod of 6.5 mmϕ. Then, the wire rod was subjected to patenting (austenitizing → isothermal transformation), shaving, annealing, and drawing processes in sequence to obtain a steel wire of 3.0 mmϕ. The patenting conditions are shown in Table 2. In this typical embodiment, the respective 6.5 mmϕ wire rods were patented under several varied patenting conditions, including austenitizing conditions under which the wire rods were heated at varied temperatures for varied retention times, and conditions for isothermal transformation under which the wire rods were heated also at varied temperatures for varied retention times-subsequentiy to the austenization, as shown in Table 2.
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[Table 1] Formulation samples Chemical composition (mass %) C Si Mn Cr Co Ni Others A 0.45 2.2 0.5 0.9 0.3 - - B 0.78 2.0 0.6 0.8 - - - C 0.68 1.6 0.5 1.0 - - - D 0.63 2.8 0.6 0.9 - - - E 0.61 2.2 1.7 1.0 - 0.3 - F 0.60 2.2 0.6 0.5 - - - G 0.64 2.3 0.5 1.7 - - - H 0.62 2.1 0.5 1.1 - - - I 0.64 2.2 0.6 1.2 - - V: 0.6 J 0.63 2.1 0.5 1.1 - - Ti: 0.3 K 0.55 2.4 0.5 1.3 0.2 - - L 0.72 2.3 0.55 1.2 0.5 - - M 0.63 1.9 1.2 1.4 - 0.3 - N 0.62 2.5 0.2 0.9 0.3 - - O 0.64 2.3 0.8 1.1 0.4 - - P 0.65 2.2 0.9 0.9 0.3 0.5 - Q 0.65 2.0 0.4 1.0 0.3 - V: 0.15 R 0.60 2.3 1.0 0.8 - - Mo: 0.20 S 0.63 2.1 0.9 1.1 0.4 0.3 Ti: 0.10 -
[Table 2] Patenting conditions Conditions Austenization Isothermal transformation Heating temperature (°C) Retention time (sec) Heating temperature (°C) Retention time (sec) I 920 120 630 80 II 980 60 700 30 III 880 120 650 50 IV 950 190 650 50 V 950 50 650 50 VI 1,070 60 650 50 VII 920 120 580 50 VIII 920 120 650 15 IX 920 120 650 120 X 920 120 780 50 - The resultant steel wires (3.0mmϕ) were then subjected to quenching-tempering. For the quenching, the conditions shown in Table 3 were used, while the tempering was carried out using a heating temperature of 450-530°C for all wires. The reduction of area (RA) and the average grain sizes (average γ grain size) of austenite grains (prior austenite grains) were measured on the respective quench-tempered wires. The results are shown in Table 3. Further, the wire quenching temperature was varied to change the average grain size of austenite grains (prior austenite grains). The average grain size of austenite grains was determined based on the intercept method subject to JIS G 0522.
- Further, the shear yield stress and the fatigue properties (fatigue limit) were measured on those steel wires which were subjected, after the quenching-tempering, to heat treatment (420°C for 2 hours or 480°C for 2 hours) comparable to nitriding treatment. The results are shown also in Table 3. The shear yield stress of the steel wires which were heat-treated as above was determined from torque-θ curves obtained through twisting tests on samples of 100d in length (d: sample diameter). The fatigue limit was evaluated based on a Nakamura-type rotating bending fatigue test.
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[Table 3] No. Samples Conditions Quenching temperature (°C) Average γ grain size (µm) RA (%) Shear yield stress 420°C×2hr Shear yield stress 480°C×2hr Fatigue limit (MPa) 1 A I 920 4.5 45 985 892 715 2 B II 930 4.8 35 955 864 705 3 C I 920 4.3 48 938 821 730 4 D I 950 5.4 37 941 823 735 5 E II - - - - - - 6 F II 940 5.0 42 923 815 720 7 G II - - - - - - 8 H I 930 4.4 45 921 810 705 9 H I 850 2.8 31 928 815 715 10 H I 1,050 8.9 50 925 810 710 11 I II 920 3.8 29 925 835 695 12 J I 910 3.5 41 930 830 705 13 K I 930 4.3 46 1,098 1,021 850 14 L II 910 3.2 43 1,130 1,043 865 15 M II 940 5.2 48 1,178 1,098 875 16 N I 1,020 6.5 44 1,084 1,015 855 17 O I 980 6.2 45 1,195 1,078 875 18 P II 950 5.2 48 1,168 1,054 880 19 Q II 930 3.5 45 1,121 1,038 865 20 R I 920 3.4 47 1,154 1,069 870 21 S I 940 4.4 46 1,211 1,113 895 - As shown in Table 3, it is understood that the steel wires of samples No. 13 through 21 having a 40% or higher reduction of area (RA) and a 1,000 MPa or higher shear yield stress after the heat treatment comparable to nitriding treatment all have a high fatigue limit. Moreover, since the steel wires of these samples have a high shear yield stress, it is considered that these steel wires will be excellent in their permanent set properties. Thus, it is understood that the spring steel wire of the present invention is provided with high toughness while having excellent fatigue properties.
- On the other hand, the samples No. 1-4, 6, and 8 having a low shear yield stress after the heat treatment comparable to nitriding treatment turned out to have a low fatigue limit. Especially, the samples No.2 and 4 had also an inferior toughness with a low reduction of area. Further, the steel wires of the samples No. 5 and 7 underwent martensite generation in their wire rod structures during patenting and then frequent wire breakage in the succeeding shaving step, and thus the experiment was forced to stop continuing. For the sample No. 11, since it had a higher V content of the total steel in addition to its low shear yield stress after the heat treatment, it had a lowered reduction of area of the steel wire to thus reduce its fatigue limit. For the sample No. 12, since it had a higher Ti content in addition to its low shear yield stress after the heat treatment, it underwent a reduction in fatigue limit owing to breakage caused by Ti-based inclusions.
- For the sample No. 9, since it had a smaller average grain size of the austenite grains (prior austenite grains) in addition to its low shear yield stress after the heat treatment, it showed also a low reduction of area. On the other hand, the sample No. 10 showed a reduction in fatigue limit, because it had a large average grain size of the austenite grains (prior austenite grains) in addition to its low shear yield stress after the heat treatment.
- In the same manner as the above-described embodiment, a steel having the chemical compositions of the sample K of Table 1 was worked to prepare a wire rod of 6.5mmϕ, and the resultant wire rod was then worked into a steel wire of 3.0mmϕ likewise as above. In this case, the patenting conditions employed were varied as shown in Table 2. The wire thus obtained was subjected to quenching-tempering (quenching temperature: 940°C, tempering temperature: 450-530°C), and the reduction of area (RA) of the resultant wire and its average grain size of the austenite grains (prior austenite grains) were measured. The results are shown in Table 4. Further, the shear yield stress and the fatigue properties (fatigue limit) were measured on those steel wires which were subjected, after the quenching-tempering, to heat treatment (420°C for 2 hours or 480°C for 2 hours) comparable to nitriding treatment. The results are shown together with the temperature conditions in Table 4. Measurement of the physical properties was carried out like the preceding examples.
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[Table 4] No. Samples Conditions Quenching temperature (°C) Average γ grain size (µm) RA (%) Shear yield stress 420°C×2hr Shear yield stress 480°C×2hr Fatigue limit (MPa) 22 K I 940 4.5 45 1,098 1,021 865 23 K II 940 4.5 46 1,083 1,015 860 24 K III 940 4.4 37 930 824 730 25 K IV - - - - - - 26 K V 940 4.3 36 934 829 728 27 K VI - - - - - - 28 K VII - - - - - - 29 K VIII - - - - - - 30 K IX 940 4.6 35 932 823 731 31 K X 940 4.7 36 925 815 734 - As shown in Table 4, it is understood that the samples No. 22 and 23 which were patented under particular conditions (austenitization: 900-1,050°C for 60 to 180 seconds, isothermal transformation: 600-750°C for 20 to 100 seconds) both had a high fatigue limit.
- However, since the samples No. 25, and 27-29 underwent martensite generation in their wire rod structures during patenting and then frequent wire breakage in the drawing step, the experiment was forced to stop continuing. In the samples No. 24 and 26, since there remained undissolved carbide, the wires each had a lowered reduction of area and a reduced fatigue limit. Moreover, the samples No. 24 and 26 each had also a low shear yield stress. The samples No. 30 and 31 underwent cementite spheroidization in their wire rod structures so that there remained undissolved carbide, which resulted in reduced reduction of area and lower shear yield stress of each steel wire.
- Since the spring steel wire of the present invention is excellent both in fatigue properties and in toughness, it is best suited as a material for springs that are used for parts requiring an adequate fatigue strength.
Claims (13)
- A spring steel wire having a tempered martensitic structure brought about by quenching-tempering, the spring steel wire comprising:a 40 % or higher reduction of area; anda 1,000 Mpa or higher shear yield stress after subjected to heat treatment for at least 2 hours at a temperature ranging from 420°C to 480°C.
- The spring steel wire according to claim 1 consisting of, based on mass %, C: 0.50-0.75%, Si: 1.80-2.70%, Mn: 0.1-0.7%, Cr: 0.70-1.50%, Co: 0.02-1.0%, and remnants consisting of Fe and impurities.
- The spring steel wire according to claim 1 consisting of, based on mass %, C: 0.50-0.75%, Si: 1.80-2.70%, Mn: over 0.7-1.5%, Cr: 0.70-1.50%, and remnants consisting of Fe and impurities.
- The spring steel wire according to claim 1 consisting of, based on mass %;
C: 0.50-0.75%, Si: 1.80-2.70%, Mn: over 0.7-1.5%, Cr: 0.70-1.50%;
at least one element of Ni: 0.1-1.0% and Co: 0.02-1.00%; and
remnants consisting of Fe and impurities. - The spring steel wire according to claim 1 consisting of, based on mass %;
C: 0.50-0.75%, Si: 1.80-2.70%, Mn: 0.1-0.7%, Cr: 0.70-1.50%, Co: 0.02-1.00%;
at least one element selected from the group of 5 elements consisting of V: 0.05-0.50%, Mo: 0.05-0.50%, W: 0.05-0.15%, Nb: 0.05-0.15% and Ti: 0.01-0.20; and
remnants consisting of Fe and impurities. - The spring steel wire according to claim 1 consisting of, based on mass %;
C: 0.50-0.75%, Si: 1.80-2.70%, Mn: over 0.7-1.5%, Cr: 0.70-1.50%;
at least one element selected from the group of 5 elements consisting of V: 0.05-0.50%, Mo: 0.05-0.50%, W: 0.05-0.15%,
Nb: 0.05-0.15% and Ti: 0.01-0.20%; and
remnants consisting of Fe and impurities. - The spring steel wire according to claim 1 consisting of, based on mass %, C: 0.50-0.75%, Si: 1.80-2.70%, Mn: over 0.7-1.5%, Cr: 0.70-1.50%, at least one element of Ni: 0.1-1.0% and Co: 0.02-1.00%, at least one element selected from the group of 5 elements consisting of V: 0.05-0.50%, Mo: 0.05-0.50%, W: 0.05-0.15%, Nb: 0.05-0.15% and Ti: 0.01-0.20%, and remnants consisting of Fe and impurities.
- The spring steel wire according to any one of the claims 1 through 7 comprising austenite grains (prior austenite grains) which have an average grain size in the range of 3.0-7.0 µm.
- A spring manufactured from the spring steel wire according to any one of the claims 1 through 7.
- A spring manufactured from the spring steel wire according to claim 8.
- A method of manufacturing a spring steel wire, comprising the steps of:patenting a steel consisting of chemical compositions given below;drawing the thus patented steel into a steel wire; andsubjecting the resultant steel wire to quenching-tempering;wherein said patenting process comprises:an austenization step in which the steel is heated at 900-1,050°C for 60 to 180 seconds; andan isothermal transformation step in which the thus austenized steel is heated at 600-750°C for 20 to 100 seconds;Chemical compositions (based on mass %):
C: 0.50-0.75%, Si: 1.80-2.70%, Mn: 0.1-0.7%, Cr: 0.70-1.50%,
Co: 0.02-1.00%, and remnants consisting of Fe and impurities. - A method of manufacturing a spring steel wire, comprising the steps of:patenting a steel consisting of chemical compositions given below;drawing the thus patented steel into a steel wire; andsubjecting the resultant steel wire to quenching-tempering;wherein said patenting process comprises:an austenization step in which the steel is heated at 900-1,050°C for 60 to 180 seconds; andan isothermal transformation step in which the thus austenized steel is heated at 600-750°C for 20 to 100 seconds;Chemical compositions (based on mass %):
C: 0.50-0.75%, Si: 1.80-2.70%, Mn: over 0.7-1.5%, Cr: 0.70-1.50%, and remnants consisting of Fe and impurities. - A method of manufacturing a spring steel wire, comprising the steps of:patenting a steel consisting of chemical compositions given below;drawing the thus patented steel into a steel wire; andsubjecting the resultant steel wire to quenching-tempering;wherein said patenting process comprises:an austenization step in which the steel is heated at 900-1,050°C for 60 to 180 seconds; andan isothermal transformation step in which the thus austenized steel is heated at 600-750°C for 20 to 100 seconds;Chemical compositions (based on mass %):
C: 0.50-0.75%, Si: 1.80-2.70%, Mn: over 0.7-1.5%, Cr: 0.70-1.50%, at least one element of Ni: 0.1-1.0% and Co: 0.02-1.00%, and remnants consisting of Fe and impurities.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004027891A JP4357977B2 (en) | 2004-02-04 | 2004-02-04 | Steel wire for spring |
PCT/JP2005/001703 WO2005075695A1 (en) | 2004-02-04 | 2005-02-04 | Steel wire for spring |
Publications (3)
Publication Number | Publication Date |
---|---|
EP1731625A1 true EP1731625A1 (en) | 2006-12-13 |
EP1731625A4 EP1731625A4 (en) | 2012-03-28 |
EP1731625B1 EP1731625B1 (en) | 2019-10-09 |
Family
ID=34835907
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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EP05709768.5A Expired - Fee Related EP1731625B1 (en) | 2004-02-04 | 2005-02-04 | Steel wire for spring |
Country Status (6)
Country | Link |
---|---|
US (1) | US20080271824A1 (en) |
EP (1) | EP1731625B1 (en) |
JP (1) | JP4357977B2 (en) |
KR (1) | KR101096888B1 (en) |
CN (1) | CN100449026C (en) |
WO (1) | WO2005075695A1 (en) |
Families Citing this family (19)
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JP5114665B2 (en) * | 2006-03-31 | 2013-01-09 | 新日鐵住金株式会社 | Heat-treated steel for high-strength springs |
US8684594B2 (en) | 2008-11-17 | 2014-04-01 | The Foundation: The Research Institute For Electric And Magnetic Materials | Magnetically insensitive, highly hard and constant-modulus alloy, and its production method, as well as hair spring, mechanical driving apparatus and watch and clock |
DE102009042954A1 (en) * | 2009-09-24 | 2011-04-07 | Webasto Ag | Control rod for an adjustable closing element of a vehicle roof |
US8349095B2 (en) * | 2009-09-29 | 2013-01-08 | Chuo Hatsujo Kabushiki Kaisha | Spring steel and spring having superior corrosion fatigue strength |
JP5711539B2 (en) | 2011-01-06 | 2015-05-07 | 中央発條株式会社 | Spring with excellent corrosion fatigue strength |
KR101289104B1 (en) | 2011-11-08 | 2013-07-23 | 주식회사 포스코 | Wire rod, steel wire and manufacturing method of steel wire |
JP6208611B2 (en) | 2014-03-31 | 2017-10-04 | 株式会社神戸製鋼所 | High strength steel with excellent fatigue properties |
WO2016001706A1 (en) * | 2014-07-03 | 2016-01-07 | Arcelormittal | Method for producing a high strength steel sheet having improved strength and formability and obtained sheet |
EP3346020B1 (en) * | 2015-09-04 | 2020-07-29 | Nippon Steel Corporation | Spring steel wire and spring |
CN105648332A (en) * | 2016-01-27 | 2016-06-08 | 太仓捷公精密金属材料有限公司 | High-performance spring steel |
KR102061806B1 (en) | 2017-10-23 | 2020-01-02 | (주)포스코케미칼 | Thermal spray materials for Flange repair of RH Snorkel |
KR102120699B1 (en) * | 2018-08-21 | 2020-06-09 | 주식회사 포스코 | Wire rod and steel wire for spring with improved toughness and corrosion fatigue resistance and method for manufacturing the same |
CN109972038B (en) * | 2019-04-01 | 2021-07-20 | 宝钢特钢韶关有限公司 | Steel for ultra-deep well drill rod joint and manufacturing method thereof |
WO2021167072A1 (en) * | 2020-02-21 | 2021-08-26 | 日本製鉄株式会社 | Damper spring |
CN112143869B (en) * | 2020-09-27 | 2022-08-12 | 广州市奥赛钢线科技有限公司 | Preparation process of quenched and tempered spring steel wire with tensile strength of 2300-2400 MPa |
CN114318125A (en) * | 2020-09-30 | 2022-04-12 | 宝山钢铁股份有限公司 | High-strength and high-toughness alloy tool steel wire and manufacturing method thereof |
CN112427484B (en) * | 2020-11-11 | 2022-07-26 | 南京工程学院 | Method for manufacturing stainless spring steel wire through recrystallization annealing regulation and control |
KR102492641B1 (en) * | 2020-12-17 | 2023-01-30 | 주식회사 포스코 | Wire rod and steel wire for spring, spring with improved fatigue resistance and nitriding properties, and the method for manufacturing the same |
CN113881897A (en) * | 2021-09-29 | 2022-01-04 | 东莞市锦中秀寝具用品有限公司 | High-strength alloy material for spring and high-strength spring |
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JPH10251795A (en) * | 1997-03-12 | 1998-09-22 | Honda Motor Co Ltd | Oil tempered steel wire for spring excellent in delayed fracture resistance |
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- 2004-02-04 JP JP2004027891A patent/JP4357977B2/en not_active Expired - Fee Related
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2005
- 2005-02-04 US US10/588,287 patent/US20080271824A1/en not_active Abandoned
- 2005-02-04 WO PCT/JP2005/001703 patent/WO2005075695A1/en active Application Filing
- 2005-02-04 EP EP05709768.5A patent/EP1731625B1/en not_active Expired - Fee Related
- 2005-02-04 CN CNB2005800039621A patent/CN100449026C/en not_active Expired - Fee Related
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JPH10251795A (en) * | 1997-03-12 | 1998-09-22 | Honda Motor Co Ltd | Oil tempered steel wire for spring excellent in delayed fracture resistance |
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Also Published As
Publication number | Publication date |
---|---|
JP2005220392A (en) | 2005-08-18 |
WO2005075695A1 (en) | 2005-08-18 |
KR101096888B1 (en) | 2011-12-22 |
JP4357977B2 (en) | 2009-11-04 |
US20080271824A1 (en) | 2008-11-06 |
CN100449026C (en) | 2009-01-07 |
KR20060129019A (en) | 2006-12-14 |
EP1731625B1 (en) | 2019-10-09 |
EP1731625A4 (en) | 2012-03-28 |
CN1914347A (en) | 2007-02-14 |
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