CN109338247A - A kind of cobalt improved austenitic stainless steel of copper zirconium and its process and heat treatment method - Google Patents

A kind of cobalt improved austenitic stainless steel of copper zirconium and its process and heat treatment method Download PDF

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CN109338247A
CN109338247A CN201811576377.6A CN201811576377A CN109338247A CN 109338247 A CN109338247 A CN 109338247A CN 201811576377 A CN201811576377 A CN 201811576377A CN 109338247 A CN109338247 A CN 109338247A
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stainless steel
rolling
heat treatment
cold
alloy
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罗丰华
罗硕
卢静
周伟
吴子恺
杜帅
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Central South University
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Central South University
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/50Ferrous alloys, e.g. steel alloys containing chromium with nickel with titanium or zirconium
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D1/00General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
    • C21D1/18Hardening; Quenching with or without subsequent tempering
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
    • C21D8/0226Hot rolling
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
    • C21D8/0236Cold rolling
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0247Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
    • C21D8/0273Final recrystallisation annealing
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/02Ferrous alloys, e.g. steel alloys containing silicon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/04Ferrous alloys, e.g. steel alloys containing manganese
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/42Ferrous alloys, e.g. steel alloys containing chromium with nickel with copper
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/52Ferrous alloys, e.g. steel alloys containing chromium with nickel with cobalt
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/58Ferrous alloys, e.g. steel alloys containing chromium with nickel with more than 1.5% by weight of manganese
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/001Austenite
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Abstract

A kind of cobalt improved austenitic stainless steel of copper zirconium and its process and heat treatment method, alloying element mass percent are as follows: C≤0.03, Ni=8.0~12.0, Cr=18.0~20.0, Zr≤0.53, Cu=0.2~0.8, Co=0.1~0.5, Mn≤2.0, Si≤1.0, P≤0.035, S≤0.030, wherein 7.59 × C≤Zr≤7.59 × C+0.3, surplus Fe.Through thermal deformation cogging and cold deformation, ZrC is broken, disperse, grain coarsening after higher temperature solid solution.Contain 5 × 10 for 80 DEG C under the conditions of logical oxygen‑6F0.5mol/L H2SO4Corrosion electric current density is 1.12~1.94 μ A/cm in electrolyte2, suitable with the stainless steel double polar plate material through surface covering.Have the characteristics that soft and high extension, conducive to the molding of bipolar plate runner.

Description

A kind of cobalt improved austenitic stainless steel of copper zirconium and its process and heat treatment method
Technical field
The invention belongs to field of Austenitic stainless steel, be related to high corrosion-resistant austenitic stainless steel ingredient design and processing, Heat-treating methods can be widely used for the energy, electric power, chemical field and daily life.
Technical background
Fuel cell is that a kind of chemical energy by between hydrogen fuel and oxidant is directly translated into electric energy by electrode reaction Device.Since its is high-efficient, pollution is small, the time of founding the factory is short, reliability and maintainability are good, be after hydroelectric generation, thermal power generation, Forth generation generation technology after nuclear power.In numerous fuel cells, Proton Exchange Membrane Fuel Cells is later one of development Kind new fuel cell, but its is with the fastest developing speed.
In a fuel cell, play support, afflux, segmentation oxidant and reducing agent and Oxidizing and Reducing Agents is guided to exist The conductive separator plate that electrode surface flows in battery is referred to as bipolar plates.Inside fuel cell unit, the function and feature of bipolar plates To separate oxidant and reducing agent, therefore bipolar plates must have the function of choke, cannot use porous air pervious material;Make with afflux With, it is necessary to it is the good conductor of electricity.Environment locating for bipolar plates exists simultaneously oxide isolation such as oxygen and reducing medium such as hydrogen, institute With bipolar plate material must be able under these conditions in the potential range of its work have resistance to corrosion.Bipolar plates should be heat Good conductor, to ensure that the temperature of battery pack is uniformly distributed and the implementation of heat extraction scheme.
The two sides of bipolar plates, which process or are equipped with, makes the equally distributed runner of reaction gas, i.e., so-called flow field, and flow field should be true It protects reaction gas to be evenly distributed everywhere in entire electrode, bipolar plates also play support membrane electrode in fuel cell unit, keep electricity The stable effect of pond pile structure, this requires plate materials to have certain intensity, and bipolar plate material answers that light, intensity is good, simultaneously And it is suitable for batch production.
It is the principal element for being difficult to commercial applications at present that cost is too high, and lower quality is than high power and volume ratio Power is also its big obstacle in automobile power power supply application aspect.Generally, the expense of bipolar plates not only accounts for always in cost Cost, and occupy cell reaction heap weight.Therefore, seek and design inexpensive, lightweight, plate it is thin, have good mechanical property Energy, high surface and bulk conductivity, low-permeable, resistant material and lower-cost technology of preparing are bipolar plates development Target.
The bipolar plates being widely used at present have graphite plate, metal plate and composite dual-electrode plates.
Graphite bi-polar plate has good rotproofness, electric conductivity, and the contact resistance on surface is small.Thus in a variety of materials In bipolar plates, the discharge performance of graphite bi-polar plate is best, is often used as developing the reference frame of other new material bipolar plates.But stone The porosity of ink is big, mechanical strength is low, brittleness is big, poor processability, in order to prevent working gas from seeping bipolar plates and meet machine The thickness of tool Intensity Design, graphite bi-polar plate should be thicker, and it is larger that this allows for its volume and weight, to limit graphite bi-polar The practical application of plate.The auto industry of especially great application prospect, it is desirable that necessary gravimetric specific energy with higher, and can It is subjected to the vibration of automobile during high speed exercise.
Not only obdurability is good for metal material, but also machining property, electric conductivity, thermal conductivity, compactness are preferable, can be with For making very thin bipolar plates.But all metals all have one disadvantage in that that is, corrosion resistance is poor, this allows for needing to use Various technologies are improved its performance with means.
The electrochemical behavior of 316L, 317L, 349 and 904L stainless steel are carried out pair under analog fuel cell operating conditions Than the corrosion resistance sequence obtained are as follows: 349 > 904L > 317L > 316L shows that chromium content is higher, and corrosion resistance is stronger.Without The passivation layer that the 316L stainless steel of surface treatment is formed in fuel cell environment will lead to contact resistance increase, not be able to satisfy double The requirement of plate material.Therefore, the corrosion resistance to enhance stainless steel, it is necessary to or painting plating modified to its surface.
The corrosion occurred in fuel cell operation to solve stainless steel and titanium plate as bipolar plate material and surface Problem of passivation, using the methods of thermal jet, silk-screen printing, physical vapour deposition (PVD), chemical vapor deposition, plating, chemical plating and sputtering, Such surface treatment not only reduces contact resistance, but also improves the corrosion resistance of bipolar plates.
At simulated battery cathode working environment (0.8V/NHE, 80 DEG C, air), to being coated with 10nm thickness nm Au 316L stainless steel carries out constant potential polarization for 24 hours, and corrosion electric current density is less than 1 μ A/cm2.It is constantly under anode-context Passive state.After bipolar plates are made in its punching press, in the case where assembling force is 0.6MPa, contact resistance is 6.3m Ω cm2
Niobium metal is plated on 316L stainless steel using ion implantation technique, in simulation Proton Exchange Membrane Fuel Cells building ring (0.5mol/L H under border2SO4+ 2ppm HF, 80 DEG C), the stainless steel watch after ion implanting 2h reveals best performance, electrokinetic potential Testing its lower passive current density is 6 μ A/cm2
The amorphous of 3 μ m-thicks densification is prepared on 316L stainless steel using closed field unbalanced magnetron sputtering ion plating method Carbon-coating.In the case where assembling force is 1.2~2.1MPa, contact resistance is 8.3~5.2m Ω cm2, and the contact resistance of graphite is 10.4~5.4m Ω cm2.(0.5mol/L, H under simulated battery working environment2SO4+ 2ppm HF, 80 DEG C), it is moved Potential test, cathode passive current density are 3.56 μ A/cm2
The features such as in the metal material of all researchs, stainless steel material is cheap with its, solid durable, becomes earliest Metal material for bipolar plates.The corrosion resistance of stainless steel material be largely determined by the formed passivation layer in its surface at Point and structure, and be passivated composition of layer and structure and determined again by the chemical component of stainless steel, therefore suitably stainless steel material alloy Change and organizational controls, have certain influence to its corrosion resisting property.
Summary of the invention
The object of the present invention is to provide a kind of cobalt improved austenitic stainless steel of copper zirconium and its process and heat treatment methods.This hair For bright its technical problem of solution the technical scheme adopted is that on the basis of 304L austenitic stainless steel alloy ingredient, addition is strong Solid solution element copper (Cu), cobalt (Co), abbreviation 304L-CCZ stainless steel under carbide former zirconium (Zr) and high temperature.Its specifically at Divide (mass percent) are as follows: C≤0.03, Ni=8.0~12.0, Cr=18.0~20.0, Zr≤0.53, Cu=0.2~0.8, Co=0.1~0.5, Mn≤2.0, Si≤1.0, P≤0.035, S≤0.030, wherein 7.59 × C≤Zr≤7.59 × C+0.3, Fe=surplus.It after alloy smelting, is handled through overheating deforming cogging and cold deformation, so that the ZrC formed is able to sufficiently broken, disperse Distribution, then by higher temperature solid solution, obtain coarse grain austenite structure, make it have higher-strength and corrosion resistance.
304L stainless steel be low C 304 steel, under general state, corrosion resistance is similar to 304 steel, but after welding or After person eliminates stress, anti-grain boundary corrosion ability is outstanding;In the case where not being heat-treated, also it is able to maintain good anti-corrosion Property, use -196 DEG C~800 DEG C of temperature.Reveal in field applied to the demanding chemistry of anti-grain boundary corrosion, coal, Petroleum Industry The part that its machine, the heat-resisting part of building materials and heat treatment are had any problem.The performance indicator of its plate are as follows: yield strength >=175MPa, Tensile strength >=480MPa, elongation >=40%, hardness≤200HV.
Contain the C not higher than 0.03% in 304L stainless steel.C in austenitic stainless steel is imitated with stronger solution strengthening Fruit, but C is easy to form cementite Fe in conjunction with Fe3C is precipitated in lamella, the corrosion resistance of stainless steel is caused to be difficult to improve.Therefore, Carbide Zr is added in the alloy, the spherical particle ZrC compound of high stability is formed, so that austenite The solid solution content of practical C is greatly lowered in crystal grain, improves the corrosion resistance of stainless steel.Since the atomic weight of Zr is 91.22, and C Atomic weight be 12.01, the atomic weight ratio of Zr, C is 7.59, as 7.59 × C≤Zr≤7.59 × C+0.3, as C content is When 0.03%, the content of Zr is 0.22%~0.52%, so that the solid solution of C is close to zero in austenite grain, and less than 0.3% Zr element surplus, with matrix formed solid solution, have weaker reinforcing and toughening effect.
Cu is non-carbide forming element, is added in steel and will form substitution solid solution.The Cu of every addition 1.0% can in steel The solution strengthening effect of 38~70MPa is generated, and copper adds the increment that caused yield strength increment is higher than tensile strength, And then the yield tensile ratio of steel can be improved significantly.The Cu ion for not luring steel surface to dissolve out can destroy bacterium internal protein structure, Inhibit the duplication and the synthesis of related protein/enzyme of DNA of bacteria, destroys the metabolic activity in bacterium, so that bacterium is lost activity, lead Cause bacterial death.Therefore 1~3%Cu is often added in some weathering steel, improves the corrosiveness of the resistance to marine environment of alloy.
A small amount of Cu is added in the present invention, the deficiency of C element when being to make up high-temperature heat treatment there are one significance. There are a large amount of Cr, Ni element in austenitic stainless steel, the segregation of Cr, Ni element be also cause the corrosion resistance of stainless steel be difficult into The main reason for one step improves.Therefore it needs to promote Cr, Ni to spread and homogenize in soak, and the presence of C element, have Conducive to the diffusivity for improving alloying element.Due to being added to carbide in the present invention, so that austenite grain Middle C solid solution content is very low, is unfavorable for homogenizing, it is therefore desirable to supplement a small amount of Cu, improve diffusivity, overcome Cr, Ni element Segregation further increases corrosion resistance.
Co is the element of non-carbide, is ferrite former, can form continuous solid solution with ferrite.Cobalt can drop The harden ability of low steel, cobalt can increase diffusion velocity of the carbon in austenite, to accelerate phase transition process, reduce the through hardening of steel Property.Cobalt not only accelerates the high-temperature phase-change process (austenite → pearlite) of steel, and influence middle temperature transformation process (austenite → Bainite).Co is added on a small quantity in austenitic stainless steel, phase-state change will not be caused, since the atomic radius of cobalt is 1.26, slightly Less than the atomic radius 1.27 of iron, therefore the Co atom being dissolved into Fe matrix is capable of forming tensile stress field, reduces stainless steel Hardness.
Bipolar plates two sides have and make the equally distributed runner of reaction gas, i.e., so-called flow field.These runners are by being rolled into Type obtains, and bipolar plate material hardness is low, can reduce the rebound generated when calendering and stress is concentrated.Co reduces the hard of stainless steel Degree, is conducive to the processing in flow field.
The preparation method of the 304L-CCZ stainless steel includes following key step:
(1) smelting and casting of 304L-CCZ stainless steel
Selection electrical pure iron, crome metal piece, metal nickel plate, stainless steel waste material, fine copper block, pure cobalt piece, ferrozirconium or metal zirconium, Graphite block is raw material, after electric arc melting or induction melting, is cast into alloy cast ingot.
It, should not be raw using stainless steel industries such as Converter vacuum oxygen decarburization methods since alloy is added to the elements such as Cu, Zr, Co Production method can only prepare alloy using electric arc melting or induction melting method.It takes vacuum or argon gas to protect when melting, avoids oxygen Change.
Stainless steel waste material is mainly that 304,304L etc. has nickelic, Gao Ge austenitic stainless steel waste material, then pure with electrician The raw materials such as iron, crome metal piece, metal nickel plate, fine copper block, pure cobalt piece, ferrozirconium or metal zirconium, graphite block, the 304L-CCZ not Become rusty alloyage in the composition range of steel, controls the essential elements such as C, Cr, Ni, Cu, Zr, Co in alloy, and Mn, Si, P, S etc. Impurity element is guaranteed by the purity of raw material.
Bath temperature is kept for 1700 DEG C ± 20 DEG C when melting;Molten steel calmness 5~10 minutes before being poured, molten steel 1550 DEG C ± 50 DEG C, vacuum or argon for protecting pouring.According to subsequent product specification needs, the side's of being cast as ingot or billet.
(2) hot rolling cogging
Plate uses flat roll mill hot rolling cogging, and hot rolling scheme is that slab is heated to 1280 DEG C ± 10 DEG C, and heat preservation 3~5 is small When after come out of the stove rolling, hot rolling start temperature is 1180 DEG C ± 20 DEG C, finishing temperature >=950 DEG C.Plate hot rolling is always lower to measure >=60%.
Hot forging, groove rolling or universal rolling cogging can be used in pipe, stick, line, profile and cold punching part, ingot casting.
(3) cold-rolling deformation
Plate uses cold-rolling deformation, cold rolling overall reduction >=80%.
The purpose of hot rolling and cold rolling is that the carbide in alloy is sufficiently broken;After big cold rolling reduction advantageously ensures that Coarse brilliant tissue is formed when continuous heat treatment.
Pipe, stick, line, profile can be used reciprocating type tube rolling, groove rolling, universal rolling or the method dialled drawn to carry out cold change Shape obtains size, the specification of product requirement;The stainless steel parts that mechanical industry needs can also use thermal deformation cogging raw material, It is obtained again by cold stamping.
(4) high-temperature heat treatment
It after cold deformation, is made annealing treatment at 1085 DEG C ± 30 DEG C, soaking time is 30 minutes~120 minutes, when heating Using the inert gas shieldings such as vacuum or argon gas, nitrogen, helium;After annealing, using the gases such as water, oil or argon gas, nitrogen helium Medium is quickly cooled down.
The purpose of soak is to form coarse recrystal grain, so that breaked spherical particle carbide is from crystal boundary It is transferred to inside coarse recrystal grain, to mitigate grain boundary corrosion tendency.It is quickly cooled down in addition to can be to avoid a small amount of remnants Outside the crystal boundary of carbide is precipitated, most important purpose is to control the segregation of Cu element, improves the solid solubility of Cu element, obtains high Intensity and hardness.
According to the requirement of the size of product and Surface Quality, cooling medium is selected, when product size is larger, can be adopted The liquid mediums such as water intaking, oil, which are realized, to be quickly cooled down, and thin plate or small part can take the fast quickly cooling of the gas mediums such as argon gas, nitrogen helium But.
The implementation of above-mentioned high-temperature heat treatment method can be used heating in vacuum-air quenching, laser heating-water hardening, continuously add Heat-high pressure gas quenching, gas shield heating-water (oil) are quenched.Carried out after annealing aligning or setting treatment, aligning or sizing at The deflection of reason should be less than 2%.
304L-CCZ stainless steel by above-mentioned high-temperature heat treatment is corroded using Ta Feier (Tafel) line extrapolation Electric current as the foundation of comparative alloy corrosion resistance, and measures the hardness and tensile mechanical properties of alloy.
Ta Feier (Tafel) line extrapolation is a kind of method for measuring corrosion rate.Way is that electricity is made in metal sample Pole is immersed in corrosive medium, is measured volt-ampere (E~I) data of stable state, is made log | I |~E figure, and by the straight of negative anodic polarization curve Line part extends.Corresponding gained intersection point is logIcor, by corrosion current IcorDivided by the sample area of prior precise measurement S0To get corrosion rate.This method is quickly time saving, the measurement suitable for metal homogeneous corrosion.
It simulates under Proton Exchange Membrane Fuel Cells working environment, therefore selects 80 DEG C to carry out corrosive nature as test temperature Comparison.The specific determination condition of corrosion rate are as follows: with 1cm2Stainless steel is working electrode, using saturated calomel electrode as reference electricity Pole, using platinized platinum as auxiliary electrode;Containing 5 × 10-6F-0.5mol/L H2SO4Electrolyte is heated to 80 DEG C with water bath, and to electricity Oxygen is passed through with the flow velocity of 20ml/min in solution liquid;Linear sweep voltametry, sweep speed 2mV/s are carried out to sample.With electrification The potentiostat function of learning constant potential tester or electrochemical workstation completes measurement, and the test software using instrument is to measuring Polarization curve carries out Ta Feier (Tafel) fitting, obtains corrosion current.The 304L stainless steel of above method measurement is rotten in room temperature Erosion electric current is 25 μ A/cm2, it is 659 μ A/cm at 80 DEG C2
Of the invention is mainly characterized by the basis of 304L stainless steel alloy, adds carbide Zr, drop The solid solubility of practical C in low austenite grain;It adds Cu element and improves High temperature diffusion ability, avoid Cr, Ni Element segregation;Addition Co element reduces stainless steel hardness;Subsequently through thermal deformation, cold deformation, causes carbide broken, is quenched by high temperature, Coarse grain is formed, so that alloy softens, and there are superior anti-corrosion abilities.304L-CCZ alloy after high temperature quenching treatment For corrosion current under the conditions of logical oxygen, 80 DEG C contain 5 × 10-6F-0.5mol/L H2SO4It is 1.12~1.94 μ A/ in electrolyte cm2, corrosion rate is greatly lowered, suitable with the corrosion rate of the bipolar plate of stainless steel through surface coated treatment.Hardness is 165 ~176HV1, yield strength are 183~192MPa, and tensile strength is 574~592MPa, and elongation percentage 43~49% has low hard Degree and high extension feature, are particularly conducive to the forming processes of bipolar plate runner.
Detailed description of the invention
3 corrosion surface electron microscope scanning figure of Fig. 1 present example;
4 polarization curve of Fig. 2 present example;
5 tensile mechanical properties curve graph of Fig. 3 present example.
Specific embodiment
Various method of smelting of the invention, casting method are not limited by following examples, any to want in right of the invention The improvements and changes in range for asking book claimed are all within protection scope of the present invention.
Selection electrical pure iron, crome metal piece, metal nickel plate, stainless steel waste material, fine copper block, pure cobalt piece, ferrozirconium or metal zirconium, Graphite block is raw material, is configured to alloy in the composition range that invention requires.
For the requirement of shape, dimensions and surface quality, prepared stainless steel and its part are subsequent that machine can be used Tool processing, polishing and corresponding chemical cleaning and polishing treatment, the present invention is not specifically limited.
Embodiment 1
Choosing electrical pure iron, crome metal piece, metal nickel plate, 304 stainless steel waste materials, fine copper block, pure cobalt piece, metal zirconium is original Material, the stainless composition of steel of configuration are as follows: C=0.03, Ni=9.5, Cr=20.0, Zr=0.22, Cu=0.2, Co=0.1, Mn =1.2, Si=0.8, P≤0.035, S≤0.030, Fe=surplus.
After weighing good corresponding raw material according to component requirements proportion, argon arc melting, bath temperature is protected when melting Hold 1720 DEG C;Calm 10 minutes of molten steel before being poured, molten steel is at 1600 DEG C, argon for protecting pouring.
Plate uses flat roll mill hot rolling cogging, and hot rolling scheme is that slab is heated to 1290 DEG C, and heat preservation is come out of the stove after 5 hours rolls System, hot rolling start temperature are 1190 DEG C, and finishing temperature is 950 DEG C.Always lower amount is 60% to plate hot rolling.
Plate uses cold-rolling deformation, and cold rolling overall reduction is 80%.
Plate is made annealing treatment at 1115 DEG C, and soaking time is 30 minutes, is protected when heating using argon gas;After annealing, Using water quenching cooling.
For the corrosion current of 304L-CCZ alloy after high temperature quenching treatment under the conditions of logical oxygen, 80 DEG C contain 5 × 10-6F-'s The H of 0.5mol/L2SO4It is 1.46 μ A/cm in electrolyte2.The hardness of alloy is 170HV1, yield strength 184MPa, and tension is strong Degree is 574MPa, elongation percentage 47%.
Embodiment 2
Choosing 304L stainless steel waste material, fine copper block, pure cobalt piece, ferrozirconium is raw material, and the stainless composition of steel of configuration is as follows: C= 0.014, Ni=8.0, Cr=18.8, Zr=0.30, Cu=0.3, Co=0.5, Mn=1.2, Si=0.7, P≤0.035, S≤ 0.030, Fe=surplus.
After weighing good corresponding raw material according to component requirements proportion, through vacuum induction melting, bath temperature is kept when melting 1680℃;Calm 5 minutes of molten steel before being poured, molten steel is at 1500 DEG C, vacuum pouring.
Plate uses flat roll mill hot rolling cogging, and hot rolling scheme is that slab is heated to 1270 DEG C, and heat preservation is come out of the stove after 5 hours rolls System, hot rolling start temperature are 1160 DEG C, and finishing temperature is 1000 DEG C.Always lower amount is 65% to plate hot rolling.
Plate uses cold-rolling deformation, and cold rolling overall reduction is 85%.
Plate keeps the temperature 120 minutes at 1055 DEG C, and helium air quenching is taken after vacuum annealing.
For the corrosion current of 304L-CCZ alloy after high temperature quenching treatment under the conditions of logical oxygen, 80 DEG C contain 5 × 10-6F-'s The H of 0.5mol/L2SO4It is 1.64 μ A/cm in electrolyte2.The hardness of alloy is 176HV1, yield strength 183MPa, and tension is strong Degree is 585MPa, elongation percentage 43%.
Embodiment 3
Choosing electrical pure iron, crome metal piece, metal nickel plate, fine copper block, pure cobalt piece, ferrozirconium, graphite block is raw material, configuration Stainless composition of steel is as follows: C=0.025, Ni=10.0, Cr=19.0, Zr=0.36, Cu=0.4, Co=0.2, Mn=0.8, Si =0.5, P≤0.035, S≤0.030, Fe=surplus.
After weighing good corresponding raw material according to component requirements proportion, induction melting is protected through argon gas, bath temperature when melting Kept for 1700 DEG C;Calm 7 minutes of molten steel before being poured, molten steel is at 1550 DEG C, argon for protecting pouring.
Plate uses flat roll mill hot rolling cogging, and hot rolling scheme is that slab is heated to 1280 DEG C, and heat preservation is come out of the stove after 4 hours rolls System, hot rolling start temperature are 1180 DEG C, and finishing temperature is 980 DEG C.Always lower amount is 70% to plate hot rolling.
Plate uses cold-rolling deformation, and cold rolling overall reduction is 82%.
Plate is made annealing treatment at 1100 DEG C, and soaking time is 60 minutes, using nitrogen protection;Take continuous annealing furnace Annealing, is quickly cooled down after annealing with high pressure nitrogen.
For the corrosion current of 304L-CCZ alloy after high temperature quenching treatment under the conditions of logical oxygen, 80 DEG C contain 5 × 10-6F-'s The H of 0.5mol/L2SO4It is 1.72 μ A/cm in electrolyte2, Fig. 1 is the electron microscope scanning figure of its corrosion surface.Alloy it is hard Degree is 165HV1, yield strength 189MPa, tensile strength 590MPa, elongation percentage 44%.
From fig. 1, it can be seen that corrosion surface is very smooth, crystal grain is very coarse, does not remain corrosion product, but has many smooth Aperture, is mainly distributed on intra-die, and crystal boundary is seldom.It falls off this is because the tiny carbide in surface preferentially corrodes, it is remaining Smooth surface is homogeneous, and crystal boundary is clear, has stronger resistance to corrosion.
Embodiment 4
Choosing 304L stainless steel waste material, fine copper block, pure cobalt piece, metal zirconium, graphite block is raw material, the stainless composition of steel of configuration It is as follows: C=0.016, Ni=8.9, Cr=18.0, Zr=0.32, Cu=0.5, Co=0.3, Mn=1.3, Si=0.3, P≤ 0.035, S≤0.030, Fe=surplus.
After weighing good corresponding raw material according to component requirements proportion, through vacuum induction melting, bath temperature is kept when melting 1690℃;Calm 8 minutes of molten steel before being poured, molten steel is at 1550 DEG C, vacuum pouring.The side's of being cast as ingot.
Ingot casting uses hot rolling cogging, and hot rolling scheme is that slab is heated to 1290 DEG C, rolling of coming out of the stove after keeping the temperature 3 hours, Hot rolling initial forging temperature is 1200 DEG C, and finishing temperature is 1020 DEG C, and always lower amount is 68% for hot rolling.
Plate uses cold-rolling deformation, and cold rolling overall reduction is 85%.
It is made annealing treatment after cold rolling at 1105 DEG C, soaking time is 45 minutes, and vacuum annealing, oil quenching are used when heating.
For the corrosion current of 304L-CCZ alloy after high temperature quenching treatment under the conditions of logical oxygen, 80 DEG C contain 5 × 10-6F-'s The H of 0.5mol/L2SO4It is 1.28 μ A/cm in electrolyte2, Fig. 2 is its corrosion test polarization curve.The hardness of alloy is 171HV1, yield strength 192MPa, tensile strength 579MPa, elongation percentage 45%.
Embodiment 5
Choosing electrical pure iron, crome metal piece, metal nickel plate, fine copper block, pure cobalt piece, ferrozirconium, graphite block is raw material, configuration Stainless composition of steel is as follows: C=0.027, Ni=12.0, Cr=18.5, Zr=0.45, Cu=0.7, Co=0.4, Mn=0.6, Si =0.3, P≤0.035, S≤0.030, Fe=surplus.
After weighing good corresponding raw material according to component requirements proportion, through argon atmosphere electric arc melting, bath temperature when melting Kept for 1700 DEG C;Calm 6 minutes of molten steel before being poured, molten steel is at 1580 DEG C, argon for protecting pouring.Plate uses flat roll mill hot rolling Cogging, hot rolling scheme are that slab is heated to 1280 DEG C, and rolling of coming out of the stove after keeping the temperature 4 hours, hot rolling start temperature is 1180 DEG C, finish to gauge Temperature is 1000 DEG C.Always lower amount is 65% to plate hot rolling.
Plate uses cold-rolling deformation, and cold rolling overall reduction is 85%.
Plate is made annealing treatment at 1100 DEG C, and soaking time is 90 minutes, is heated and is used vacuum protection when keeping the temperature, protects High pressure argon gas air quenching is used after temperature.
For the corrosion current of 304L-CCZ alloy after high temperature quenching treatment under the conditions of logical oxygen, 80 DEG C contain 5 × 10-6F-'s The H of 0.5mol/L2SO4It is 1.12 μ A/cm in electrolyte2.The hardness of alloy is 174HV1, yield strength 190MPa, and tension is strong Spending is 596MPa, elongation percentage 48%, and tensile mechanical properties curve is shown in Fig. 3.
Embodiment 6
Choosing 304L stainless steel waste material, fine copper block, pure cobalt piece, ferrozirconium, graphite block is raw material, and the stainless composition of steel of configuration is such as Under: C=0.03, Ni=10.2, Cr=18.5, Zr=0.52, Cu=0.8, Co=0.26, Mn=1.2, Si=0.6, P≤ 0.035, S≤0.030, Fe=surplus.
After weighing good corresponding raw material according to component requirements proportion, through vacuum induction melting, bath temperature is kept when melting 1710℃;Calm 8 minutes of molten steel before being poured, molten steel is at 1580 DEG C, vacuum pouring.
Plate uses flat roll mill hot rolling cogging, and hot rolling scheme is that slab is heated to 1290 DEG C, and heat preservation is come out of the stove after 4.5 hours Rolling, hot rolling start temperature are 1180 DEG C, and finishing temperature is 1050 DEG C.Always lower amount is 80% to plate hot rolling.
Plate uses cold-rolling deformation, and cold rolling overall reduction is 88%.
Plate is made annealing treatment at 1065 DEG C, and soaking time is 85 minutes, cold using nitrogen gas protection and oil.
For the corrosion current of 304L-CCZ alloy after high temperature quenching treatment under the conditions of logical oxygen, 80 DEG C contain 5 × 10-6F-'s The H of 0.5mol/L2SO4It is 1.94 μ A/cm in electrolyte2.The hardness of alloy is 173HV1, yield strength 189MPa, and tension is strong Degree is 587MPa, elongation percentage 49%.
The performance detection of the preparation process of above-described embodiment 304L-CCZ alloy obtained is as described below:
1. pair example alloy material carries out hardness test, load 1Kg, after making a call to 5 points using HVS-50 Vickers It is averaged, is listed in table 1.
2. pair example alloy material carries out stretching experiment using almighty test machine, the nominal section of sample having a size of 1~2 × The rectangular specimen of 5 × 30mm takes the average value of the tensile strength of 3 same treatment samples, yield strength and elongation percentage to be listed in table 1
3. pair example alloy carries out corrosion current measurement, the condition of test are as follows: with corruption using CHI660D electrochemical workstation Erosion face area is 1cm2Example alloy is working electrode, using saturated calomel electrode as reference electrode, using platinized platinum as auxiliary electrode;Contain 5×10-6F-0.5mol/L H2SO4Electrolyte is heated to 80 DEG C with water bath, and into electrolyte with the flow velocity of 20ml/min It is passed through oxygen;Linear sweep voltametry, sweep speed 2mV/s are carried out to sample.It is averaged after measuring 3 samples, is listed in table 1.
The ingredient and corrosion current, hardness and tensile property of 1 embodiment of table
The ingredients such as Mn, Si, P, S of each embodiment meet alloy invention and require in table 1, and Fe is surplus, is not arranged in table 1 Out.

Claims (5)

1. a kind of cobalt improved austenitic stainless steel of copper zirconium, it is characterised in that: each element mass percent in alloy are as follows: C≤0.03, Ni=8.0~12.0, Cr=18.0~20.0, Zr≤0.53, Cu=0.2~0.8, Co=0.1~0.5, Mn≤2.0, Si≤ 1.0, P≤0.035, S≤0.030, wherein 7.59 × C≤Zr≤7.59 × C+0.3, surplus Fe.
2. the process and heat treatment method of the cobalt improved austenitic stainless steel of copper zirconium as described in claim 1, it is characterised in that packet Include following steps:
(1) smelting and casting of stainless steel
By each element mass percent of alloy requirement, electrical pure iron, crome metal piece, metal nickel plate, stainless steel waste material, pure is chosen Copper billet, pure cobalt piece, ferrozirconium or metal zirconium, graphite block are raw material, after electric arc melting or induction melting, are cast into alloy casting Ingot;
Bath temperature is kept for 1700 DEG C ± 20 DEG C when melting;Molten steel calmness 5~10 minutes before being poured, molten steel is at 1550 DEG C ± 50 DEG C, vacuum or argon gas protective casting, the side's of being cast as ingot or billet;
(2) hot rolling cogging
Plate uses flat roll mill hot rolling cogging, and hot rolling scheme is after slab is heated to 1280 DEG C ± 10 DEG C, heat preservation 3~5 hours It comes out of the stove rolling, hot rolling start temperature is 1180 DEG C ± 20 DEG C, finishing temperature >=950 DEG C;Plate hot rolling is always lower to measure >=60%;Pipe, Hot forging, groove rolling or universal rolling cogging can be used in stick, line, profile and cold punching part, ingot casting;
(3) cold-rolling deformation
Plate uses cold-rolling deformation, cold rolling overall reduction >=80%;
Pipe, stick, line, profile using reciprocating type tube rolling, groove rolling, universal rolling or draw the method dialled to carry out cold deformation, obtain Size, the specification of product requirement;
(4) high-temperature heat treatment
It after cold deformation, is made annealing treatment at 1085 DEG C ± 30 DEG C, soaking time is 30 minutes~120 minutes, and when heating uses Vacuum or protective gas protection;After annealing, it is quickly cooled down using water, oil or protective gas medium;
For the corrosion current of alloy under the conditions of logical oxygen, 80 DEG C contain 5 × 10-6F-0.5mol/L H2SO4In electrolyte for 1.12~ 1.94μA/cm2, corrosion rate is greatly lowered, suitable with the corrosion rate of the bipolar plate of stainless steel through surface coated treatment;Firmly Degree is 165~176HV1, and yield strength is 183~192MPa, and tensile strength is 574~592MPa, elongation percentage 43~49%, tool There are soft and high extension feature, is conducive to the forming processes of bipolar plate runner.
3. the process and heat treatment method of the cobalt improved austenitic stainless steel of copper zirconium as claimed in claim 2, it is characterised in that: institute State protective gas are as follows: argon gas, nitrogen or helium.
4. the process and heat treatment method of the cobalt improved austenitic stainless steel of copper zirconium as claimed in claim 2, it is characterised in that: step Suddenly high-temperature heat treatment method described in (4) is with heating in vacuum-air quenching, laser heating-water hardening, laser heating-high pressure gas Body quenching, gas shield heating-water quenching or gas shield heating-oil quenching.
5. the process and heat treatment method of the cobalt improved austenitic stainless steel of copper zirconium as claimed in claim 2, it is characterised in that: move back Aligning or setting treatment are carried out after fire, align or the deflection of setting treatment is less than 2%.
CN201811576377.6A 2018-12-22 2018-12-22 A kind of cobalt improved austenitic stainless steel of copper zirconium and its process and heat treatment method Withdrawn CN109338247A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110484836A (en) * 2019-09-24 2019-11-22 哈尔滨工程大学 A kind of hafnium zirconium titanium molybdenum enhancing austenitic stainless steel and preparation method thereof
CN110607490A (en) * 2019-09-24 2019-12-24 南京佑天金属科技有限公司 Hafnium zirconium titanium reinforced austenitic stainless steel and preparation method thereof
CN111304415A (en) * 2020-02-26 2020-06-19 江阴康瑞成型技术科技有限公司 Machining process of austenitic stainless steel medical instrument part

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110484836A (en) * 2019-09-24 2019-11-22 哈尔滨工程大学 A kind of hafnium zirconium titanium molybdenum enhancing austenitic stainless steel and preparation method thereof
CN110607490A (en) * 2019-09-24 2019-12-24 南京佑天金属科技有限公司 Hafnium zirconium titanium reinforced austenitic stainless steel and preparation method thereof
CN110607490B (en) * 2019-09-24 2021-03-26 南京佑天金属科技有限公司 Hafnium zirconium titanium reinforced austenitic stainless steel and preparation method thereof
CN111304415A (en) * 2020-02-26 2020-06-19 江阴康瑞成型技术科技有限公司 Machining process of austenitic stainless steel medical instrument part
CN111304415B (en) * 2020-02-26 2022-03-04 江苏康瑞新材料科技股份有限公司 Machining process of austenitic stainless steel medical instrument part

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