CN1458983A - Piston ring excellent in resistance to scuffing, cracking and fatigue and method for producing same, and combination of piston ring and cylinder block - Google Patents
Piston ring excellent in resistance to scuffing, cracking and fatigue and method for producing same, and combination of piston ring and cylinder block Download PDFInfo
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- CN1458983A CN1458983A CN01815763A CN01815763A CN1458983A CN 1458983 A CN1458983 A CN 1458983A CN 01815763 A CN01815763 A CN 01815763A CN 01815763 A CN01815763 A CN 01815763A CN 1458983 A CN1458983 A CN 1458983A
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- 238000004519 manufacturing process Methods 0.000 title description 8
- 239000011651 chromium Substances 0.000 claims abstract description 70
- 150000004767 nitrides Chemical class 0.000 claims abstract description 60
- 229910000831 Steel Inorganic materials 0.000 claims abstract description 37
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 37
- 239000010959 steel Substances 0.000 claims abstract description 37
- 229910001220 stainless steel Inorganic materials 0.000 claims abstract description 24
- 239000010935 stainless steel Substances 0.000 claims abstract description 24
- 238000005121 nitriding Methods 0.000 claims abstract description 21
- 229910052750 molybdenum Inorganic materials 0.000 claims abstract description 10
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 10
- 239000002245 particle Substances 0.000 claims abstract description 9
- 239000012535 impurity Substances 0.000 claims abstract description 7
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- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 29
- 229910000734 martensite Inorganic materials 0.000 claims description 29
- 238000010791 quenching Methods 0.000 claims description 27
- 230000000171 quenching effect Effects 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 7
- 229910001018 Cast iron Inorganic materials 0.000 claims description 6
- 238000005266 casting Methods 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract description 19
- 229910052721 tungsten Inorganic materials 0.000 abstract description 5
- 229910052758 niobium Inorganic materials 0.000 abstract description 4
- 229910052748 manganese Inorganic materials 0.000 abstract description 2
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- 239000010410 layer Substances 0.000 description 39
- 230000000052 comparative effect Effects 0.000 description 31
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- 150000001875 compounds Chemical class 0.000 description 23
- 238000012360 testing method Methods 0.000 description 14
- 229910052742 iron Inorganic materials 0.000 description 13
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- 238000005496 tempering Methods 0.000 description 11
- 230000000694 effects Effects 0.000 description 10
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- 229910002804 graphite Inorganic materials 0.000 description 6
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- 239000000463 material Substances 0.000 description 4
- JAWMENYCRQKKJY-UHFFFAOYSA-N [3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-ylmethyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-en-8-yl]-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]methanone Chemical compound N1N=NC=2CN(CCC=21)CC1=NOC2(C1)CCN(CC2)C(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F JAWMENYCRQKKJY-UHFFFAOYSA-N 0.000 description 3
- 229910001566 austenite Inorganic materials 0.000 description 3
- 230000008859 change Effects 0.000 description 3
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- 229910000975 Carbon steel Inorganic materials 0.000 description 2
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- QKJXFFMKZPQALO-UHFFFAOYSA-N chromium;iron;methane;silicon Chemical compound C.[Si].[Cr].[Fe] QKJXFFMKZPQALO-UHFFFAOYSA-N 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
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- VLHWNGXLXZPNOO-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-3-(2-morpholin-4-ylethyl)pyrazol-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C(=NN(C=1)CC(=O)N1CC2=C(CC1)NN=N2)CCN1CCOCC1 VLHWNGXLXZPNOO-UHFFFAOYSA-N 0.000 description 1
- 229910000760 Hardened steel Inorganic materials 0.000 description 1
- 208000034189 Sclerosis Diseases 0.000 description 1
- 229910001035 Soft ferrite Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
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- 238000006396 nitration reaction Methods 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 238000010587 phase diagram Methods 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000005491 wire drawing Methods 0.000 description 1
Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/002—Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
-
- 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
- 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
- C21D9/40—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for rings; for bearing races
-
- 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
- C22C38/001—Ferrous alloys, e.g. steel alloys containing N
-
- 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
- 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
- C22C38/26—Ferrous alloys, e.g. steel alloys containing chromium with niobium or tantalum
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C8/06—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases
- C23C8/08—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases only one element being applied
- C23C8/24—Nitriding
- C23C8/26—Nitriding of ferrous surfaces
-
- 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
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pistons, Piston Rings, And Cylinders (AREA)
- Solid-Phase Diffusion Into Metallic Material Surfaces (AREA)
- Heat Treatment Of Strip Materials And Filament Materials (AREA)
Abstract
A piston ring having improved scuffing resistance, cracking resistance and fatigue resistance, consists of a high-chromium martensitic stainless steel and a sliding nitriding layer formed on the surface of said steel. The stainless steel consists of C: 0.3 to 1.0%; Cr: 14.0 to 21.0%, N: 0.05 to 0.50%, at least one of Mo, V, W and Nb: 0.03 to 3.0% in total, Si: 0.1 to 1.0%, Mn 0.1 to 1.0%, P: 0.05% or less, S: 0.05% or less, the balance being Fe and unavoidable impurities. The sliding nitriding layer comprises on its surface hard particles mainly consisting of nitrides in a range of from 0.2 to 2.0 mum of average particle size, 7 mum or less of the longest diameter, and from 5 to 30% in area ratio.
Description
Technical field
The present invention relates to be used for the piston ring of explosive motor, particularly, comprise the stainless piston ring of high martensitic chromium of nitrogenize, have resistance to marring (seizure resistance), splitting resistance (resistance to fracture) and the fatigue resistance of raising.The invention still further relates to the production method of this piston ring.
Background technology
To the demand of low fuel consumption, in light weight and high-performance explosive motor, the piston ring attenuation is with weight reduction and adapt to the high rotating speed of engine along with recently.Must improve the material behavior of piston ring, as wear resistance, resistance to marring and fatigue resistance, so that can make the piston ring attenuation.Therefore, conventional cast-iron piston ring is replaced by the piston ring of steel, particularly from fatigue resistance and stable on heating angle.But because the resistance to marring of steel pistons ring is worse than cast-iron piston ring, the sliding surface to the steel pistons ring applies surface treatment usually.The steel of piston ring is divided into carbon steel, silicon chrome steel and Martensite Stainless Steel roughly.These classification are corresponding to the dissimilar surface treatment that is added to various steel.Mainly, be that electrodeposited chromium is applied to carbon steel and silicon chrome steel.Gas nitriding is applied to Martensite Stainless Steel.Electrodeposited chromium was the most frequently used surface treatment of steel pistons ring in the past, but now the overwhelming majority replaced by nitrogenize because the resistance to marring of electrodeposited chromium is very poor under high loading, also have galvanized waste liquid to handle so that can not cause any environmental problem.
The main now high martensitic chromium stainless steel as the nitrogenize piston ring is JIS SUS440B, and component of equal value is: C:0.80-0.95%; Cr:17.0-18.0%; Si:0.25-0.50%; Mn:0.25-0.40%; Mo:0.70-1.25%; V:0.07-0.15%; All the other are Fe.When the steel nitrogenize of this component, nitrogen-atoms is from surface diffusion and get into the steel firmly and constitute nitride layer.Nitride in nitride layer mainly is the compound of Cr, V and Mo, and they can comprise solute Fe.The main component chromium of this steel is to be dissolved in the iron-based body, and also the form with the Cr carbide exists.
Because the affinity of chromium and nitrogen greater than with the affinity of carbon, when carrying out nitrogenize nitrogen when surface diffusion is entered, reacting between nitrogen and Cr carbide forms the Cr nitride.Because the Cr content height of SUS440B equivalent material makes hard Cr nitride be dispersed in the nitride layer with suitable area % to 17.0-18.0%.So nitride layer is relatively hard and improved resistance to abrasion and resistance to marring.
The Japanese laid-open nuclear patent application of publishing recently proposes the Martensite Stainless Steel of nitrogenize for 11 (1999)-No. 80907, has the resistance to marring of improvement, and it comprises Si:0.25% or still less; Mn:0.30% or still less; Among Mo, W, V and the Nb one or several: 0.3-2.5% or Cu:4.0% or still less; Ni:2.0% or still less and Al:1.5% or still less.
The patent application of Japanese laid-open nuclear discloses the M in microstructure 11 (1999)-No. 106874
7C
3The piezometric of carbide is reduced to 4.0% or during area % still less, not only the resistance to marring of piston ring steel but also workability all improve.
Though improved resistance to abrasion and resistance to marring by above-mentioned suggestion, when these piston ring are used for operating in recent explosive motor under high revolution and the high power conditions, still be easy to abrade.
So far, be to force cylinder sleeve to enter into the cylinder body of diesel motor.These engines have changed over the monoblock iron body of narrow tube distance now and have not had lining, so that weight reduction and saving cost.Always want to increase incendiary pressure from the viewpoint of waste-gas cleaning and power increase.In the microstructure of monoblock iron body, because monoblock cast(ing) has sizable rate of cooling poor, the distribution of graphite is uneven and also is uneven as the distribution of the soft Ferrite phase of scratch reason.
When the Martensite Stainless Steel piston ring combination of the cylinder surface of above-mentioned microstructure and nitrogenize, because following reason is easy to produce scratch in the beginning operational phase.
When boring and grinding (honing) polishing gas cylinder surfaces, the abrasive material of grinding miller is easy to become coarse because Ferrite is met and caused adhesion on the exhaust hood surface of boring and grinding.Because the Ferrite plastic flow is capped graphite.Therefore, because the area % of graphite reduces, the lubricated and oil storage effect of graphite is reduced.Under high combustion pressure situation, the back pressure that is added to piston ring becomes very high.Scratch often results from the crack on the piston ring outer periphery surface, extends on perpendicular to the direction of sliding.When checking nitride layer, along laminar compound test crack.Compound is thick relatively and exists along the grain boundary of iron-based body, be called as false appearance in Japanese piston ring industrial circle.Compound thin slice and the piston ring parallel distribution in surface.
In order to solve the variety of issue of piston ring, form TiN, CrN and similar compound by ion plating.Ion plating can improve resistance to abrasion and resistance to marring but the production cost height.Because the present user of cost effect is not very good to the view of ion plating.
Therefore, the purpose of this invention is to provide a kind of nitrogenize high martensitic chromium stainless steel piston ring, this ring is that cost is effective, even be applied in the diesel motor that operates in high revolution and high combustion pressure, the diesel motor of monoblock iron body particularly, neither can wear and tear, repeated stress failure can not take place in scratch, crack yet, because application meeting in the diesel motor of monoblock iron body in future in light weight constantly increases.
Specific purpose of the present invention is the grit that is adjusted in the high martensitic chromium stainless steel nitride layer, mainly is the size and the distribution of nitride, with the size that reduces the grain boundary flaky compound so that suppress fissured generation and the expansion relevant with these compounds.
A further object of the invention provides the method for producing the high martensitic chromium stainless steel piston ring.
Summary of the invention
According to editing by piston of automobile ring editorial board, the explanation that " the piston of automobile ring " that Sankaido press published in 1997 is 188 pages, when the convex surface (particularly soft phase) that focuses on micro-injustice on the sliding surface when load is gone up, because temperature heat of friction there rises, and abnormal softening and fusing takes place.This phenomenon causes the scratch of piston ring.
In the high martensitic chromium stainless steel of nitrogenize, the most of hard nitride of the microstructure ordinary representation of nitride layer are dispersed in the tempered martensitic matrix.Abrasive mechanism depends primarily on roughness micro-on the sliding surface.In nitride layer, hard particulate dispersion is in soft relatively matrix.Therefore, micro-roughness is limited by the size of grit and the state of distribution.When observation had the section of upper layer of this spline structure, following phenomenon was very clearly.Protruding grit contacts with the sliding surface on opposite, and soft relatively matrix is recessed relatively.When sliding, be retained in the lubricating oil withstanding pressure in the concave portion.Because nitriding steel has above-mentioned microstructure, so nitriding steel is very low with the whole frequency that directly contacts to face component.Therefore, the contact pressure between two slide units reduces.In addition, oil is added in the above-mentioned concave portion.So, can prevent scratch.
Hard protruding particle can obtain above-mentioned effect, has 5% or bigger to several microns with the area that scatters as long as their size is a time micron.Grit be extremely little and the few again situation of their quantity under, can not reach the effect and the effect of the protruding grit that produces according to above-mentioned mechanism.
Simultaneously, these effects are subjected to the influence of relative parts sliding surface environment.Particularly, under the situation of the above-mentioned monoblock cast-iron cylinder block that uneven texture arranged, the surface of this cylinder body is easy to become coarse on the contrary by grinding.Normally, Ferrite phase plastic flow and cover graphite.
Can improve the sliding surface of cast iron like this even be referred to as the appropriate slip that flattening-out or suitability mill by brainstrust.That is to say, following phenomenon takes place.When the coarse internal surface of cylinder when sliding becomes smoothly, removed Ferrite and exposed the graphite that is capped.Before flattening-out made progress, the oil film on the sliding surface usually was difficult to keep.The frictional force that is added in when oil film does not exist on the piston ring outer periphery surface increases.Very big frictional force is added on the outer periphery surface of piston ring repeatedly.Therefore, nitride layer constantly bears very big pressure, causes fissured generation and expansion on perpendicular to the direction of sliding.Along with the progress of suitability phenomenon on cylinder surfaces, added pressure reduces, and the disappearance crack along with the time enlarges simultaneously.As a result, nitride layer from the teeth outwards may be local by peeling, and the internal surface of cylinder is suffered damage.So, be easy to abrade in the initial stage of sliding.Therefore the compound of grain boundary is very crisp in nitride layer, and their existence has promoted fissured generation and expansion.
The present inventor finds following fundamental cause.Should mainly be the nitride of Cr with a large amount of grits of suitable dimension in the nitride layer, be dispersed in equably in the matrix in case reduce between matrix and the cylinder contact probability and so that prevent the scratch of starting stage.Particularly, the grain boundary compound that should refining forms when nitrogenize is so that reduce the fissured generation relevant with these compounds.In this very thin microstructure,, also can suppress their development even the crack produces.
When fused high martensitic chromium stainless steel solidifies, the Cr carbide of eutectic on the grain boundary of primary austenite (γ phase) (the η phase: (Cr, Fe)
7C
3) crystallization.In the high martensitic chromium stainless steel, exist maximum diameter to surpass the Cr carbide of 20 μ m (micron), as described above this steel is solidified, hot rolling then, Spheroidizing Annealing and finally quenching and tempering.About the refining of thick nascent eutectic Cr carbide, Tetsu and Hagane (Japanese iron and steel institute magazine) the 82nd volume, the 4th, 309-314 page or leaf (1996) report is by adding 0.25% or more N refining carbide.According to this report, the Cr carbide of eutectic disappears and is displaced and is on the border of nascent γ, is deposited on flaky M around the nascent γ grain boundary
23C
6And M
2N (M:Cr, Fe).These sheets are deposited in the hot rolling and divide thinlyyer.In the Spheroidizing Annealing of following, with M
2The thin M of the new deposition in the place that the N deposition is different
23C
6Therefore, whole C r carbide attenuates.
Netsushori the 36th volume, the 4th, the mechanical characteristics of the Martensite Stainless Steel of 16.5% Cr-0.65%C of 234-238 page or leaf (1996) report adding 0.25% N.That is to say that along with the increase of N content, the quenching temperature that obtains maximum hardness is transformed into lower temperature.Along with the increase extensibility of N content also increases.This explains that N increases and along with the increase of quenching temperature must be stablized austenite phase transformation at the meltage of austenite in mutually.
The patent application 9-289053 of Japanese laid-open nuclear and disclose a kind of rolling bearing 9-287058 number, its uses the method by adding N refining Cr carbide.
The present inventor after deliberation above-mentioned abrasive mechanism and relative big flaky crystalline grain border compound influence that piston ring sliding surface crack is generated and use the technology that adds N refining Cr carbide.Therefore, have been found that a large amount of nitride will be dispersed in nitride layer equably and neutralize particularly that the size of grain boundary compound will carefully be desirable.This very thin microstructure makes the high martensitic chromium stainless steel piston ring of nitrogenize that resistance to marring, splitting resistance and the fatigue resistance of raising be arranged, even operate under high revolution and the high power conditions in the explosive motor when it is used in, particularly, in the time of in the monoblock iron body diesel motor of weight reduction recently etc. also is like this.
According to the high martensitic chromium stainless steel piston ring of nitrogenize of the present invention, it is characterized in that it comprises the high martensitic chromium stainless steel, this ladle is drawn together, by weight percentage, C:0.3 to 1.0%; Cr:14.0 to 21.0%; N:0.05 to 0.50%; Among Mo, V, W and the Nb at least one, total amount is: 0.03 to 3.0%; Si:0.1 to 1.0%; Mn:0.1 to 1.0%; P:0.05% or still less; S:0.05% or still less; All the other are Fe and unavoidable impurities; With the high martensitic chromium stainless steel nitrogenize sliding layer is arranged, this layer comprises by carbide, nitride and carbonitride, it mainly is the grit that nitride is formed, with the scope of its mean diameter of grit in the nitride layer surface at 0.5 to 2.0 μ m, maximum diameter is equal to or less than 7 μ m and area % from 5 to 30%.The size of observed grain boundary compound is to be equal to or less than 20 μ m (length) in the longitudinal profile of nitride layer.There is its durometer level of nitrided surface layer of above-mentioned microstructure characteristic that enough degree of depth are arranged at Hv900 to 1400 with from the surface downwards.
Method according to the high martensitic chromium stainless steel piston ring of production nitrogenize of the present invention comprises: fusing has the steel of above-mentioned component then to add nitrogen; The steel of fusing is cast blank; Hot rolling; Annealing; Cold drawn silk; Cold rolling so that form the approximate shapes of piston ring cross section; Quench; Tempering is so that provide wire rod; Bending wire is become the shape of piston ring; Stress relieving; The rough grinding of side surface; Nitrogenize; Remove the surface compound layer; Grind butt end; The smooth grinding of side surface; Overlap joint with outer periphery surface.Before bending to the piston ring shape, to quench, temperature is low relatively as this temperature of the stainless quenching temperature of high martensitic chromium between 850 to 1000 ℃.As a result, microstructure is by refinement and contain the carbide of distribution as much as possible.Nitrogenize can be gas nitriding, ion nitriding and radical nitrogenize.In 450 to 600 ℃ of scopes of temperature, carried out nitrogenize 1 to 20 hour.
Describe the present invention below in detail.
Description is according to the stainless component of high martensitic chromium of the present invention.
C is the solute element of interstitial type among the Fe and the hardness that increases matrix.C is easy to Cr, Mo, V, W and Nb combination and constitutes carbide.Carbide mainly is converted into nitride when nitrogenize.In other words, nitride improves the resistance to abrasion and the resistance to marring of piston ring sliding surface.When C content was lower than 0.3%, the generation of sclerosis and carbide was not enough.On the other hand, when C content greater than 1.0% the time, in thick eutectic Cr carbide (the η phase: M of steel setting up period of fusing
7C
3Carbide) mass crystallization.This carbide greatly damages the workability of material in the wire production process of following.So carbon content is in 0.3 to 1.0% scope, preferably in 0.4 to 0.9% scope.
Cr is the solute element that replaces among the Fe.Chromium not only improves erosion resistance but also brings out solution strengthening thereby improve the heat resistanceheat resistant set.Here heat settability is a kind of phenomenon, and owing to creep, stress reduces to make the sealing property variation when piston ring is operated at high temperature.Cr reacts and generation Cr carbide with C in steel.These Cr carbide are easy to react with N, and nitrogen is clamp-oned from surface seepage when nitrogenize, make the Cr carbide change into the Cr nitride.The Cr nitride is dispersed in the nitride layer with the form of grit.Grit in nitride layer has greatly improved the resistance to abrasion and the resistance to marring of piston ring sliding surface.When the content of Cr less than 14% the time, the generation of Cr carbide is inadequate.On the other hand, when the content of Cr greater than 21% the time, thereby form the δ Ferrite toughness is reduced.In addition, make Ms (starting temperature that martensite transforms) so low when the concentration of Cr becomes high like this in matrix, thereby can not obtain satisfied quenching hardness.Therefore, Cr content is within 14 to 21% scope, preferably in 16 to 19% scope.
N is the same calking element in Fe with C.For example cut at 17%Cr line place, available pseudo-binary phase diagram is represented ternary Fe-Cr-C phasor.Produce eutectic reaction between Fe and C, the concentration of carbon is given by the left end of eutectic line.Before completely solidified, still have the steel of fusing on every side in the native transistors grain boundary simultaneously.The steel generation eutectic reaction of fusing when temperature further descends.When adding nitrogen according to the present invention, the concentration of above-mentioned left side C is higher than the C concentration of the molten steel of no nitrogen.Therefore, the generation of eutectic reaction and η carbide is suppressed.In the time of under temperature drops to eutectic temperature, over-saturation C and N are with sheet M
23C
6And M
2The sedimentary form of N is precipitation around primary γ crystal grain.η phase crystallization when N content is lower than 0.05%.On the other hand, when N content greater than 0.5% the time, bar-shaped M
2The N precipitation capacity increases, thereby toughness is reduced.Therefore, N content more preferably is in 0.10 to 0.30% scope in 0.05 to 0.5% scope.Solute N hinders the diffusion of C and helps crystal grain thinning border compound in matrix.This is first Fe of casting back
3C, and behind nitriding treatment, finally change into Fe
3N.Under standard atmosphere pressure, the nitrogen of height to 0.2% can be added.Being higher than 0.2% nitrogen content need be at pressure N
2Fusing adds under the atmosphere.So nitrogen content is preferred according to the viewpoint that adds nitrogen in 0.05 to 0.20% scope.
Any one all is the constitutor of carbide and can improves resistance to abrasion and resistance to marring among Mo, V, W and the Nb.In addition, Mo prevents to soften when tempering and nitriding treatment and playing a significant role aspect the dimensional stability that obtains piston ring.V promotes nitrogenize, and the hardness that therefore contains the V nitride layer is very high.Any one characteristic to the raising piston ring all is effective in these elements.When at least one total content of Mo, V, W and Nb less than 0.03% the time, in fact their effect can ignore.On the other hand, when the total content of these elements greater than 3% the time, workability is subjected to grievous injury and toughness also reduces.Therefore, at least one total content of Mo, V, W and Nb is between 0.03% to 3.0%.
Si is the reduction additive.Si also is dissolved among the Fe and improves softening resistance when tempering.Thereby can improve so-called heat resistanceheat resistant set.When Si content less than 0.1% the time, its effect is slight.On the other hand, when the content of Si greater than 1.0% the time, toughness suffers damage.Therefore, the content of Si is in 0.1 to 1.0% scope.
Mn also is the reduction additive.When Mn content less than 0.1% the time, its effect is slight.On the other hand, when Mn content greater than 1.0% the time, workability suffers damage.Therefore, Mn content is between 0.1 to 1.0%.
P and Mn and analogous element form impurity and can reduce fatigue strength and erosion resistance.P is the impurity of steel.P is few more good more.Therefore should be with the viewpoint P content of practice or still less 0.05%.Preferably, P 0.03% or still less.
S is the same with P, reduces fatigue strength and erosion resistance.S is the impurity of steel.S is few more good more.Therefore should be 0.05% or still less from the viewpoint S content of practice.Preferably, S 0.03% or still less.
Steel by above-mentioned composition range generates the microstructure that resistance to marring improves, and that is to say, has a large amount of trickle nitride particles in nitride layer.Particularly, the nitride that exists in the nitride layer surface promptly mainly is Cr nitride, carbide and carbonitride, the grit that constitutes should have mean diameter, at 0.5 to 2 μ m (micron), maximum diameter 7 μ or still less and area % in 5 to 30% scopes.When average particulate diameter during less than 0.5 μ m, the convex surface of grit is to preventing that abrasive effect from being not enough.On the other hand, when average particulate diameter during, under high loading, abrade easily greater than 2 μ m.When maximum diameter during greater than 7 μ m, the microstructure of nitride layer becomes inhomogeneous, thereby abrades easily under high loading.When area % less than 5% the time, abrade easily.On the other hand, when the area % of nitride greater than 30% the time, wire drawing and curve the piston ring shape and become difficult after the fusing.Preferred area % is between 10 to 25%.
The nitride layer microstructure that improves splitting resistance is like this, and the size (length) of observing the grain boundary compound on the piston ring longitudinal profile is 20 μ m or still less.When can being created in during greater than 20 μ m, maximum length becomes problem of cracks under the high loading easily.
Can belong to stainless microstructure according to the present invention such as above-mentioned nitride layer microstructure.At first, in continuously hot rolling, nodularization thermal treatment, cold drawn silk, quenching and tempered steel, do not exist thick eutectic Cr carbide (η mutually: (Cr, Fe)
7C
3Carbide).This obtains by adding nitrogen.
Secondly, when remain on quenching temperature, deposit before the nitrogenize a large amount of thin inferior level carbides (the ε phase, (and Cr, Fe)
23C
6Carbide).(the Fe-Cr-C phasor represents that more and thinner carbonaceous deposits is arranged in the district of γ+ε) time when quenching temperature is reduced to.When low as far as possible to (when the temperature in the district of γ+ε) is quenched, quantitatively having thin εTan Huawu as much as possible to deposit.In addition, the growth of γ crystallographic grain is suppressed, so that hardened steel is thin grain pattern.When this steel nitrogenize, it is very thin that the grain boundary compound also becomes.Therefore from above-mentioned viewpoint, preferred quenching temperature is in the scope between 850 to 1000 ℃.When quenching temperature is lower than 850 ℃, do not harden and since α deposition mutually can not obtain required hardness.When quenching temperature during greater than 1000 ℃, the coalescent and γ crystallographic grain alligatoring of carbide in the maintenance step under quenching temperature.As a result, thick carbide changes into thick nitride.The grain boundary compound chap that in the nitriding treatment of following, forms along thick γ crystallographic grain.
Nitriding treatment by the relative short period of time in the present invention obtains from the surface high rigidity of the Hv 900 to 1400 of enough degree of depth.Therefore the thin relatively γ crystallographic grain that this specific character is attributable to form under low quenching temperature has increased the border of crystal grain, the main diffusion admittance of N when these borders are nitriding treatment.
According to the present invention, in 450 to 600 ℃ temperature range, carry out nitriding treatment.Treatment temp is about 590 ℃ and once was considered to suitable temperature in the prior art, and is maximum in the solubleness of nitrogen under this temperature in α-Fe lattice.But because the present invention uses main nitrogen diffusion by the grain boundary, treatment temp is not limited in about 590 ℃.May be more suitable from the processing of the viewpoint lesser temps of piston ring dimensional stability.But from the viewpoint of practice, nitrogenize was carried out under 450 to 600 ℃ 1 to 20 hour.
Description of drawings
Fig. 1 is the back scatter electronic imaging photo with the slip nitride layer surface of sem observation.Fig. 1 (a) and (b) correspond respectively to example 1 and comparative example 1.
Fig. 2 is a nitride layer transverse section optical microscope photograph.Fig. 2 (a) and (b) correspond respectively to example 1 and comparative example 1.
Fig. 3 represents the sample of scoring test.
Fig. 4 represents the movement mechanism of wear test machine.
Fig. 5 represents the movement mechanism of piston ring protracted test machine.
Fig. 6 is the graphic representation of expression safe range of stress.
Fig. 7 is illustrated in the fissured photo that forms on the sliding surface of comparative example 13.
Embodiment
Example 1-11 (n-J11) and comparative example 1-8 (H1-H8)
Fusing has the amount of the high martensitic chromium stainless steel 10kg that is listed in component in the table 1 in the vacuum induction melting stove.But, will join less than 0.2% N in the steel when under standard atmosphere pressure, melting, simultaneously at pressurization N
2In the atmosphere when fusing with 0.2% or more N join in the steel.Wire rod by hot-work acquisition diameter 12mm carried out Spheroidizing Annealing 10 hours under 750 ℃ after pickling.The steel wire that 3.5mm * 5.0mm rectangular cross section is arranged by procedure of processing production.Steel wire is passed through quenching furnance (under the Ar protective atmosphere) and tempering stove (under the Ar protective atmosphere).After keeping approximate 10 minutes, 930 ℃ of temperature carry out air quenching.Carried out tempering about 25 minutes at 620 ℃.Steel wire is cut into the long sample of 50mm so that nitriding treatment.Carrying out gas nitriding under 570 ℃ handled 4 hours.But the quenching temperature of comparative example 1 (H1) is 1100 ℃ as conventional method.Other condition is identical with each example and other comparative examples.
Table 1
(weight percent %)
????C | ?Cr | ?N | ?Mo | ?V | ?W | ?Nb | ?Si | ?Mn | ?P | ?S | |
?J1 | ?0.65 | ?17.5 | ?0.13 | ?1.5 | ?- | ?- | ?- | ?0.25 | ?0.35 | ?0.02 | ?0.01 |
?J2 | ?0.41 | ?17.0 | ?0.19 | ?1.0 | ?0.15 | ?- | ?- | ?0.25 | ?0.50 | ?0.02 | ?0.02 |
?J3 | ?0.83 | ?17.8 | ?0.23 | ?- | ?0.20 | ?- | ?- | ?0.20 | ?0.30 | ?0.02 | ?0.02 |
?J4 | ?0.59 | ?17.2 | ?0.16 | ?- | ?- | ?0.05 | ?- | ?0.20 | ?0.20 | ?0.02 | ?0.02 |
?J5 | ?0.62 | ?17.5 | ?0.15 | ?- | ?- | ?- | ?0.3 | ?0.20 | ?0.30 | ?0.02 | ?0.02 |
?J6 | ?0.60 | ?14.5 | ?0.15 | ?1.5 | ?0.5 | ?0.1 | ?0.5 | ?0.55 | ?0.65 | ?0.02 | ?0.02 |
?J7 | ?0.60 | ?19.5 | ?0.25 | ?1.0 | ?- | ?0.1 | ?- | ?0.20 | ?0.30 | ?0.02 | ?0.02 |
?J8 | ?0.35 | ?20.3 | ?0.28 | ?1.0 | ?- | ?- | ?0.3 | ?0.20 | ?0.30 | ?0.02 | ?0.02 |
?J9 | ?0.95 | ?14.9 | ?0.25 | ?- | ?0.5 | ?0.1 | ?- | ?0.20 | ?0.30 | ?0.02 | ?0.02 |
?J10 | ?0.55 | ?16.5 | ?0.08 | ?- | ?0.5 | ?- | ?0.3 | ?0.35 | ?0.55 | ?0.02 | ?0.02 |
?J11 | ?0.48 | ?18.2 | ?0.42 | ?- | ?- | ?0.1 | ?0.3 | ?0.20 | ?0.20 | ?0.02 | ?0.02 |
?H1 | ?0.81 | ?17.5 | ?0.03 | ?1.0 | ?0.3 | ?- | ?- | ?0.25 | ?0.25 | ?0.02 | ?0.02 |
?H2 | ?0.45 | ?18.0 | ?0.58 | ?1.5 | ?0.5 | ?- | ?- | ?0.20 | ?0.20 | ?0.02 | ?0.02 |
?H3 | ?0.25 | ?17.3 | ?0.16 | ?1.0 | ?0.4 | ?- | ?- | ?0.20 | ?0.30 | ?0.02 | ?0.02 |
?H4 | ?1.12 | ?17.8 | ?0.15 | ?1.2 | ?0.6 | ?- | ?- | ?0.20 | ?0.30 | ?0.02 | ?0.02 |
?H5 | ?0.69 | ?13.2 | ?0.21 | ?1.1 | ?0.5 | ?- | ?- | ?0.20 | ?0.30 | ?0.02 | ?0.02 |
?H6 | ?0.73 | ?22.1 | ?0.22 | ?1.0 | ?0.2 | ?- | ?- | ?0.20 | ?0.20 | ?0.02 | ?0.02 |
?H7 | ?0.65 | ?17.8 | ?0.16 | ?- | ?- | ?- | ?- | ?0.20 | ?0.20 | ?0.02 | ?0.02 |
?H8 | ?0.68 | ?17.3 | ?0.15 | ?1.5 | ?1.0 | ?0.5 | ?0.5 | ?0.20 | ?0.20 | ?0.02 | ?0.02 |
It is long so that the observation of microstructure further above-mentioned steel wire sample to be cut into 10mm.Be embedded to each sample in the resin and carry out mirror finish.Use image analyzer to carry out the observation and the qualitative assessment of microstructure.The back scatter electronic imaging of the nitrided surface that slides by sem observation for example 1 (J1) and comparative example 1 (H1).The image of observed example 1 (J1) and comparative example 1 (H1) be illustrated respectively in Fig. 1 (a) and (b) in.Transverse section by the observation by light microscope nitride layer and observed photo about example 1 (n) and comparative example 1 (H1) be illustrated respectively in Fig. 2 (a) and (b) in.Grit in the scattered electrons imaging photo be overleaf deceive and be white in optical microscope photograph.Can be clear that: according to its size of grit of the present invention is minimum; With observed grain boundary its size of compound in the transverse section of nitride layer be minimum.Just sliding, average particulate diameter, largest particle diameter and the area of grit carries out qualitative assessment than % to the microstructure of example 1 to 11 (J1-J11) and comparative example 1-8 (H1-H8) in the nitrided surface.The hardness of these results and nitride layer sliding surface is listed in the table 2 together.
Table 2
* because workability difference comparative example 2,4 and 8 (H
2, H
4And H
8) can not make steel wire.Size instability after * comparative example 7 (H7) nitrogenize.So yield poorly.
The grit of slip nitride layer | The extreme length of grain boundary compound in the nitride layer transverse section (μ m) | Vickers' hardness | |||
Median size (μ m) | Maximum particle diameter (μ m) | Area occupation ratio (%) | |||
????J1 | ????1.6 | ????5 | ????17.2 | ????16 | ????1253 |
????J2 | ????1.3 | ????4 | ????13.0 | ????15 | ????1050 |
????J3 | ????1.0 | ????5 | ????22.5 | ????13 | ????1185 |
????J4 | ????1.7 | ????6 | ????15.9 | ????12 | ????1120 |
????J5 | ????1.6 | ????5 | ????17.1 | ????15 | ????1148 |
????J6 | ????1.5 | ????4 | ????10.7 | ????14 | ????955 |
????J7 | ????0.9 | ????4 | ????21.0 | ????12 | ????1219 |
????J8 | ????1.2 | ????6 | ????18.0 | ????13 | ????1193 |
????J9 | ????1.3 | ????6 | ????13.0 | ????12 | ????984 |
????J10 | ????1.8 | ????5 | ????14.2 | ????17 | ????1031 |
????J11 | ????1.2 | ????6 | ????16.2 | ????14 | ????1083 |
????H1 | ????2.7 | ????15 | ????13.6 | ????28 | ????1065 |
????H2 | ????- | ????- | ????- | ????- | ????- |
????H3 | ????1.5 | ????5 | ????7.5 | ????15 | ????830 |
????H4 | ????- | ????- | ????- | ????- | ????- |
????H5 | ????1.4 | ????5 | ????4. | ????14 | ????920 |
????H6 | ????2.2 | ????8 | ????9.1 | ????14 | ????874 |
????H7 ** | ????1.6 | ????5 | ????16.5 | ????16 | ????1109 |
????H8 | ????- | ????- | ????- | ????- | ????- |
With reference to figure 3, represent among the figure that it is the scoring test sample of Japanese alphabetical katakana " コ " form that total length 45mm is arranged.Wire rod is shaped into double end monolithic devices scoring test sample.Relative material is a disc of being made and become diameter 60mm and thickness 12mm by FC250.
The sliding surface of disk 2 (Fig. 4) is adjusted to surfaceness (Rz) 1 to 2 μ m.Use wear test machine (product of Riken company, trade mark are " Triborik I ") to carry out scoring test.The front end (reference number 1 among Fig. 4) of head is the protruding sliding surface with 20mm radius.Front end is handled through gas nitriding.Remove the thick compound layer that on front end, generates of 5 to 20 μ m (white layer) by grinding.With polishing front end is carried out mirror finish.The surfaceness (Rz) of used FC250 disk (reference number 2 among Fig. 4) sliding surface is adjusted to 1-2 μ m.The movement mechanism explanation of friction wear testing machine is in Fig. 4.Abrasive test conditions is as follows.
Sliding velocity (disk): 8 meter per seconds
Machining load: stepped start-stop system increases 0.2MPa up to scratch occurring from beginning 1.0MPa at every turn
Lubricating oil: motor oil (trade mark-Nisseki motor oil P#20)
Near lubricating oil temperature: 80 ℃ (output)
Oil bath: 100 ℃
Lubricating oil feeding amount: 40cc/ branch
Calculate the scratch surface pressure by the wear area of scratch load and sliding surface.List the scratch surface pressure that obtains for example 1-11 (j1-11) and comparative example 1-8 (H1-H8).
Table 3
Scratch surface pressure (MPa) | |
????J1 | ????454 |
????J2 | ????443 |
????J3 | ????469 |
????J4 | ????428 |
????J5 | ????458 |
????J6 | ????420 |
????J7 | ????464 |
????J8 | ????430 |
????J9 | ????441 |
????J10 | ????419 |
????J11 | ????452 |
????H1 | ????376 |
????H2 | ????- |
????H3 | ????340 |
????H4 | ????- |
????H5 | ????328 |
????H6 | ????297 |
????H7 | ????388 |
????H8 | ????- |
The resistance to marring that is clear that example 1-11 (J1-J11) has been compared raising with comparative example 1,3,5-7 (H1, H3, H5-H7).
Example 12-14 (J12-J14) and comparative example 9-11 (H9-H11)
To there be the materials processing of example 1 chemical composition to become steel wire and carry out air quenching by listed temperature in the table 4.Use the method identical to carry out the gas nitriding processing with example 1.The microstructure of quantitative analysis nitride layer.The results are shown in the table 4.
Table 4
* the hardness of comparative example 9 (H9) nitride layer is lower than Hv 860.Example 15 and comparative example 12
Quenching temperature (℃) | The grit of slip nitride layer | The extreme length of grain boundary compound in the nitride layer transverse section (μ m) | |||
Median size (μ m) | Maximum particle diameter (μ m) | Area occupation ratio (%) | |||
????H9 * | ????800 | ????0.3 | ????5 | ????15.4 | ????14 |
????J12 | ????870 | ????0.5 | ????5 | ????19.4 | ????11 |
????J13 | ????920 | ????1.3 | ????6 | ????18.5 | ????15 |
????J14 | ????980 | ????1.8 | ????6 | ????17.4 | ????18 |
????H10 | ????1030 | ????2.3 | ????9 | ????14.7 | ????31 |
????H11 | ????1080 | ????2.8 | ????11 | ????11.5 | ????49 |
Make the steel of example 1 and comparative example 1 pass through the compression ring that each procedure of processing is made rectangular cross section.Specific diameter (d
1) be 95.0mm, thickness (a
1) be 3.35mm and width (h
1) be 2.3mm.Quench by following air-cooling in 10 minutes at 930 ℃ quenching furnance.By carrying out tempering in about 25 minutes at 620 ℃ tempering stove.Carrying out successive quenches and tempering.Under 570 ℃, carry out gas nitriding 4 hours.But the quenching temperature of comparative example 12 is the same with conventional method to be 1100 ℃.Other condition is identical with comparative example 15.
The compression ring that test is produced in protracted test machine, the movement mechanism explanation of trier is in Fig. 5.Cut out the butt end of compression ring at two ends so that widen the size of free clearance.The piston ring of having handled with setter 9 such settings in trier 3 makes its reduced to specific diameter.Rotate offset cam 4 then and transmit the multiple stroke 40 times, be used for further diameter reduction, rupture up to piston ring 3 to less than specific diameter with per second.When fracture, obtain added stress number.Repeat this test, change the stress on the sample that is added to identical index simultaneously.Obtain so-called S-N figure and be illustrated in final fatigue limit diagram among Fig. 6.
With reference to figure 6, be clear that example 15 compared great improvement with comparative example 12.
Example 16-19 and comparative example 13-14
Make the steel of example 1 (example 16,17), example 7 (example 18,19) and comparative example 1 (comparative example 13,14) pass through the main body (example 17,19 and comparative example 14) that each procedure of processing is made compression ring (example 16,18 and comparative example 13) and two-piece type oil ring.Compression ring has the orthogonal cross section.Its specific diameter (d
1) be 99.2mm, thickness (a
1) be 3.8mm and width (h
1) be 2.5mm.The main body of oil ring is the saddle type cross section.Its specific diameter (d
1) be 99.2mm, thickness (a
1) be 2.5mm and width (h
1) be 3.0mm.
Identical in quenching in example 16-19, tempering and gas nitriding and the example 15.Quenching in comparative example 13-14, tempering and gas nitriding are identical with comparative example 12.
Compression ring and the oil ring produced are installed in the diesel motor of four-cylinder 3200cc discharge capacity.These rings are installed on the piston and with the monoblock cast iron housing combine, fatigue test was carried out in operation in 100 hours under following condition.Rotating speed: 3600rpm (rev/min) power: 75kW load: full load water temperature: 110 ℃ of oil temperature: abrading appearred 2 hours 10 minutes after in 130 ℃ of comparative examples 13 and abrading appearred after 7 hours 55 minutes in comparative example 14.And example 16-19 none generation problem in test.With reference to figure 7, fissured photo on the expression comparative example 13 slip nitrided surfaces among the figure.
Industrial usability
According to the present invention, in the piston ring nitration case that the nitrogenize high chromium martensitic stainless steel is made, there is a large amount of trickle nitride. Also refining flaky crystalline grain border compound. Can form such micro-structural by adding nitrogen and low temperature quenching. Because this micro-structural has improved wear resistence, resistance to marring, crack resistance and fatigue resistance. According to piston ring of the present invention, therefore can advantageously be applied in the explosive motor that works under high rotating speed and the high power conditions, particularly in the Diesel engine of recent lightweight monoblock casting. Also can advantageously be applied in the truck of fractional motor the fatigue problem of this class car possibility initial ring when using the exhaust lock according to piston ring of the present invention. Can suitably implement as the main body of two-piece type oil ring and the rail bar of three-piece oil ring according to piston ring of the present invention.
Claims (6)
1. piston ring of forming by high martensitic chromium stainless steel and the slip nitride layer that on the surface of described steel, forms, it has resistance to marring, splitting resistance and the fatigue resistance of raising, it is characterized in that described high martensitic chromium stainless steel comprises, by weight percentage, C:0.3 to 1.0%; Cr:14.0 to 21.0%; N:0.05 to 0.50%; Among Mo, V, W and the Nb at least one, total amount is 0.03 to 3.0%; Si:0.1 to 1.0%; Mn:0.1 to 1.0%; P:0.05% or still less; S:0.05% or still less; All the other are Fe and unavoidable impurities; Also have, comprise the grit of mainly being made up of nitride at its above slip nitride layer of surface, its average particle size particle size is in 0.5 to 2.0 μ m (micron) scope, and maximum diameter 7 μ m or littler and area % are 5 to 30%.
2. piston ring as claimed in claim 1 is characterized in that its size of observed grain boundary nitride (length) is 20 μ m or littler on the nitride layer longitudinal section.
3. piston ring as claimed in claim 1 or 2 is characterized in that the stainless N content of described high martensitic chromium is 0.05 to 0.20%.
4. as each described piston ring of claim 1 to 3, the hardness of the nitride layer that it is characterized in that sliding is in the scope of Hv 900 to 1400.
5. produce the method for the piston ring that resistance to marring, splitting resistance and fatigue resistance be improved by the high martensitic chromium stainless steel being carried out nitriding treatment for one kind, it is characterized in that the high martensitic chromium stainless steel comprises, by weight percentage, C:0.3 to 1.0%; Cr:14.0 to 21.0%; N:0.05 to 0.50%; Among Mo, V, W and the Nb at least one: total amount is 0.03 to 3.0%; Si:0.1 to 1.0%; Mn:0.1 to 1.0%; P:0.05% or still less; S:0.05% or still less; All the other are Fe and unavoidable impurities; And before described high martensitic chromium stainless steel is curved annular shape, it is carried out the quenching in the temperature range between 850-1000 ℃.
6. the combination of the cylinder of casting as any one described piston ring of claim 1 to 4 and cast iron monoblock.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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JP2000216255A JP4724275B2 (en) | 2000-07-17 | 2000-07-17 | Piston ring excellent in scuffing resistance, cracking resistance and fatigue resistance, and manufacturing method thereof |
JP216255/2000 | 2000-07-17 |
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CN1458983A true CN1458983A (en) | 2003-11-26 |
CN1210427C CN1210427C (en) | 2005-07-13 |
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CNB018157637A Expired - Fee Related CN1210427C (en) | 2000-07-17 | 2001-07-16 | Piston ring excellent in resistance to scuffing, cracking and fatigue and method for producing same, and combination of piston ring and cylinder block |
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US (2) | US20040040631A1 (en) |
EP (1) | EP1304393B1 (en) |
JP (1) | JP4724275B2 (en) |
KR (1) | KR100507424B1 (en) |
CN (1) | CN1210427C (en) |
AR (1) | AR029730A1 (en) |
BR (1) | BR0112573B1 (en) |
DE (1) | DE60122164T2 (en) |
TW (1) | TW521093B (en) |
WO (1) | WO2002006546A1 (en) |
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JPS59162346A (en) * | 1983-02-25 | 1984-09-13 | Hitachi Metals Ltd | Pressure ring |
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-
2000
- 2000-07-17 JP JP2000216255A patent/JP4724275B2/en not_active Expired - Lifetime
-
2001
- 2001-07-16 CN CNB018157637A patent/CN1210427C/en not_active Expired - Fee Related
- 2001-07-16 WO PCT/JP2001/006127 patent/WO2002006546A1/en active IP Right Grant
- 2001-07-16 KR KR10-2003-7000751A patent/KR100507424B1/en not_active IP Right Cessation
- 2001-07-16 AR ARP010103377A patent/AR029730A1/en active IP Right Grant
- 2001-07-16 US US10/333,326 patent/US20040040631A1/en not_active Abandoned
- 2001-07-16 EP EP01949987A patent/EP1304393B1/en not_active Expired - Lifetime
- 2001-07-16 DE DE60122164T patent/DE60122164T2/en not_active Expired - Lifetime
- 2001-07-16 BR BRPI0112573-7A patent/BR0112573B1/en not_active IP Right Cessation
- 2001-07-16 TW TW090117357A patent/TW521093B/en not_active IP Right Cessation
-
2007
- 2007-01-24 US US11/657,015 patent/US20070187002A1/en not_active Abandoned
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Also Published As
Publication number | Publication date |
---|---|
EP1304393A4 (en) | 2005-08-03 |
TW521093B (en) | 2003-02-21 |
EP1304393B1 (en) | 2006-08-09 |
KR100507424B1 (en) | 2005-08-10 |
JP4724275B2 (en) | 2011-07-13 |
JP2002030394A (en) | 2002-01-31 |
BR0112573A (en) | 2003-07-01 |
US20070187002A1 (en) | 2007-08-16 |
DE60122164T2 (en) | 2007-10-11 |
BR0112573B1 (en) | 2009-01-13 |
KR20030025275A (en) | 2003-03-28 |
CN1210427C (en) | 2005-07-13 |
AR029730A1 (en) | 2003-07-10 |
US20040040631A1 (en) | 2004-03-04 |
EP1304393A1 (en) | 2003-04-23 |
DE60122164D1 (en) | 2006-09-21 |
WO2002006546A1 (en) | 2002-01-24 |
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