WO2023036251A1 - Vacuum carburizing method for obtaining dispersedly distributed fine carbide - Google Patents

Vacuum carburizing method for obtaining dispersedly distributed fine carbide Download PDF

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Publication number
WO2023036251A1
WO2023036251A1 PCT/CN2022/117851 CN2022117851W WO2023036251A1 WO 2023036251 A1 WO2023036251 A1 WO 2023036251A1 CN 2022117851 W CN2022117851 W CN 2022117851W WO 2023036251 A1 WO2023036251 A1 WO 2023036251A1
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Prior art keywords
carburizing
temperature
stage
pulse
quenching
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PCT/CN2022/117851
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French (fr)
Chinese (zh)
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丛培武
徐跃明
杜春辉
陆文林
陈旭阳
何龙祥
王赫
薛丹若
杨广文
范雷
凡占稳
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中国机械总院集团北京机电研究所有限公司
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Publication of WO2023036251A1 publication Critical patent/WO2023036251A1/en

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    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C8/00Solid 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
    • C23C8/06Solid 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
    • C23C8/08Solid 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
    • C23C8/20Carburising
    • 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
    • C21D1/00General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
    • C21D1/74Methods of treatment in inert gas, controlled atmosphere, vacuum or pulverulent material
    • C21D1/773Methods of treatment in inert gas, controlled atmosphere, vacuum or pulverulent material under reduced pressure or vacuum
    • 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
    • C21D11/00Process control or regulation for heat treatments
    • C21D11/005Process control or regulation for heat treatments for cooling

Definitions

  • the invention relates to a vacuum carburizing heat treatment technology, in particular to a variable temperature vacuum carburizing method for obtaining dispersed fine carbides.
  • Heat treatment is a process technology that gives or improves the service performance of the workpiece by changing the microstructure inside the workpiece, or changing the chemical composition of the workpiece surface, and fully exploits the potential of the material.
  • Heat treatment is a key core technology in the machinery manufacturing industry. With the continuous emphasis on heat treatment technology, the heat treatment industry has gradually developed from extensive to refined, and more attention has been paid to new processes, new technologies, improving product intrinsic quality, saving energy, reducing consumption and prolonging life. Focus on economic benefits, etc. Vacuum low-pressure carburizing technology gradually replaces controllable atmosphere carburizing equipment with the advantages of less oxidation, energy saving and emission reduction, and clean heat treatment. It is more and more widely used in key parts such as gears and transmission shafts.
  • Heavy-duty gears, shafts and other key load-bearing parts are widely used in aerospace, wind power, high-speed locomotives, heavy-duty vehicles and other industries. It is generally required to be "hard on the outside and tough on the inside", and the surface layer is usually strengthened by carburizing and quenching. Studies have shown that increasing the carbon content of the carburized layer and obtaining fine, well-formed and well-distributed carbides is very beneficial to the strength and toughness of the heat-treated workpiece, and the surface hardness is as high as 800-1000HV1.
  • One object of the present invention is to provide a variable temperature vacuum carburizing method for obtaining dispersed fine carbides, which can increase the carbon content of the carburized layer while avoiding harmful network carbides, so as to realize the external hardness of the material.
  • the method has the advantages of short technological process, high carburizing efficiency, cleanness and pollution-free, and strong practicability.
  • variable temperature vacuum carburizing method for obtaining dispersed fine carbides of the present invention includes a heating and heat preservation stage, a pulse carburizing stage, a variable temperature stage, and a quenching stage;
  • the pulse carburizing stage includes alternately performing multiple carburizing cycles and diffusion cycles at the carburizing temperature, wherein in the carburizing cycle, the carburizing gas is pulsed into the carburizing chamber, and the carbon concentration gradient of the surface layer of the workpiece and The effective hardened layer depth can be adjusted by the number of alternate carburizing cycles and the diffusion cycle and the duration of each time.
  • the carbon content of the surface layer of the workpiece is close to the carbon in the austenite at the carburizing temperature. the maximum solubility;
  • the temperature changing stage includes: filling the carburizing chamber with cooling gas after the pulse carburizing stage to rapidly cool the surface layer of the workpiece to a temperature below 700°C and stabilize it for a period of time, so that carbides are uniformly precipitated and Spheroidizing, then evacuate to vacuum, immediately raise the temperature to the quenching temperature of 750°C to 980°C and hold it for a period of time, so that the workpiece is evenly heated and completely austenitized;
  • any one of the following quenching methods is selected: direct high-pressure gas quenching, direct oil quenching, and gas-oil composite quenching.
  • At least one intermediate temperature change stage and at least one second pulse carburizing stage are included before the temperature change stage; the intermediate temperature change stage includes filling the carburizing chamber with cooling gas The surface layer of the workpiece is rapidly cooled to a temperature below 700°C and stabilized for a period of time, so that the carbides are uniformly precipitated and spheroidized, and then vacuumed, and the temperature is immediately raised to the temperature required for the second pulse carburizing stage.
  • the alternating times and duration of each carburizing period and diffusion period in the second pulse carburizing stage and the respective carburizing periods and diffusion periods in the pulse carburizing stage are at least partially different.
  • the carburizing temperature is 750 to 980°C
  • the carburizing pressure is 800 to 1500Pa
  • the total time of the carburizing cycle and the The ratio of the total time of the diffusion cycle is 1:2 to 1:7.
  • the pressure of the cooling gas is ⁇ 2 ⁇ 10 5 Pa, and the holding time after cooling down to a temperature below 700°C is 5 to 60 minutes.
  • the holding time after the temperature is 750°C to 980°C is 5 to 120 minutes.
  • the carburizing gas is acetylene or propane
  • the cooling gas is nitrogen, argon or helium.
  • the duration of the pulse carburizing stage is ⁇ 30 minutes.
  • the duration of the pulse carburizing stage is ⁇ 120 minutes.
  • variable temperature vacuum carburizing method for obtaining dispersed fine carbides adopts alternate carburizing cycles and diffusion cycles in the pulse carburizing stage and adjusts their cycle numbers and Cycle time, to obtain the required carbon concentration gradient curve; in the variable temperature stage, the surface layer of the workpiece is rapidly cooled by pressurized air to uniformly precipitate carbides and refine the structure.
  • the treated member can obtain dispersed fine carbides, so as to realize the principle of the treated member being hard on the outside and tough on the inside. target properties.
  • the method has the advantages of short technological process, high carburizing efficiency, cleanness and no pollution, and strong practicability, so that the treated material can obtain better strength and toughness, and the service performance of the material is improved.
  • Fig. 1 is a schematic diagram of the traditional process curve of vacuum low-pressure carburizing in the prior art
  • Fig. 2 is the schematic diagram of the curve of temperature and pressure changing with time of the variable temperature vacuum carburizing method of an embodiment of the present invention
  • Fig. 3 is the topography diagram of the carbide structure on the surface of the shaft treated by the traditional vacuum low-pressure carburizing method in the prior art, with a magnification of 500;
  • Figure 4a is a topography diagram of carbides on the surface of the shaft treated by the variable temperature vacuum carburizing method according to an embodiment of the present invention, with a magnification of 500;
  • Fig. 4b is a SEM spherical carbide microstructure diagram of a shaft treated by a variable temperature vacuum carburizing method according to an embodiment of the present invention
  • Fig. 5 is a schematic diagram of curves of temperature and pressure changing with time in a variable temperature vacuum carburizing method according to another embodiment of the present invention.
  • Fig. 6a is a fine carbide structure topography diagram of a gear treated by a variable temperature vacuum carburizing method according to another embodiment of the present invention, with a magnification of 500;
  • Fig. 6b is a fine carbide microstructure diagram of the gear treated by the vacuum pulse carburizing method without any variable temperature stage, with a magnification of 500;
  • Fig. 7 is the hardness-depth distribution curve of the carburized layer of the gear treated by the variable temperature vacuum carburizing method according to another embodiment of the present invention.
  • Fig. 8 is the contact fatigue damage accumulation curve of the gear treated by the variable temperature vacuum carburizing method according to another embodiment of the present invention.
  • the numerical ranges should be understood as specifically disclosing all the ranges formed by the pairing of any upper limit, lower limit and preferred value within the numerical range , regardless of whether the range is explicitly stated; for example, if the numerical range "2-8" is stated, then the numerical range should be interpreted as including “2-7", “2-6", “5-7” , “3 ⁇ 4 and 6 ⁇ 7", “3 ⁇ 5 and 7", “2 and 5 ⁇ 7” and other ranges. Unless otherwise indicated, numerical ranges recited herein include their endpoints and all integers and fractions subsumed within the numerical range.
  • variable temperature vacuum carburizing method for obtaining dispersed fine carbides of the present invention includes a heating and heat preservation stage, a pulse carburizing stage, a variable temperature stage, and a quenching stage;
  • the pulse carburizing stage includes alternate carburizing cycles and diffusion cycles, wherein carburizing gas is pulsed into the carburizing chamber during the carburizing cycle, and the carbon concentration gradient and effective hardened layer depth on the surface of the workpiece can pass through the carburizing cycle.
  • the number of times the carburizing cycle and the diffusion cycle are alternated and the duration of each time are adjusted; in some embodiments, after the pulse carburizing stage, the carbon content on the surface of the material is close to the carbon at the carburizing temperature Maximum solubility in austenite;
  • the temperature changing stage includes: filling the carburizing chamber with cooling gas to quickly cool the surface of the workpiece to a temperature below 700°C, that is, the temperature below the Acl line, and stabilize it for a period of time, so that the carbides are uniformly precipitated and spheroidized. Then evacuate to a vacuum, immediately raise the temperature to the quenching temperature of 750°C-980°C, that is, 30-50°C above the Ac3 or Ac1 line, and keep it warm for a period of time, so that the workpiece is evenly heated and completely austenitized;
  • any one of the following quenching methods is selected: direct high-pressure gas quenching, direct oil quenching, and gas-oil quenching.
  • the heating and heat preservation stage it can be determined whether the heating process is segmented according to the material and size of the workpiece, and the heating temperature, heating time, and heat preservation time of each segment can be set. After the heating curve is compiled, the workpiece is placed in a vacuum furnace to evacuate and heated according to the heating curve.
  • the carburizing temperature is 750 to 980°C, and the carburizing pressure is 800 to 1500Pa.
  • the number of carburizing cycles and diffusion cycles and the duration of each cycle are based on the required effective hardened layer depth. Or determined by the carbon concentration gradient curve, the ratio of the total time of the carburizing cycle to the total time of the diffusion cycle is 1:2 to 1:7, and the value of the surface carbon content can be set at 0.8% to 2.0%, preferably 0.8% to 1.3% .
  • acetylene or propane atmosphere is selected as the carburizing gas.
  • the duration of the pulse carburizing phase is ⁇ 30 minutes. In some embodiments, the duration of the pulse carburizing phase is > 120 minutes.
  • the carburizing chamber is filled with cooling gas with a pressure ⁇ 2 ⁇ 10 5 Pa, the temperature is lowered to below 700°C and then kept for 5 to 60 minutes, and the temperature is raised to the quenching temperature of 750°C to 980°C and then kept for heat preservation 5 to 120 minutes.
  • nitrogen, argon or helium is selected as the gas filled into the carburizing chamber.
  • the pulse carburizing stage an acetylene or propane atmosphere is introduced under vacuum conditions, and the high temperature causes active carbon atoms to diffuse in the solid material and form carbides, and the surface hardening of the material is achieved after cooling.
  • the pulse carburizing stage is very critical. The duration and alternating times of the carburizing cycle and the diffusion cycle directly affect the carbon concentration gradient curve on the surface of the material, which in turn affects the microstructure and properties of the material, the carburizing temperature and the total carburizing The length of time determines whether the austenite grains will grow.
  • the workpiece In the temperature-changing stage after the end of pulse carburizing, the workpiece remains in the vacuum carburizing chamber, the heating is stopped, and nitrogen, argon or helium is charged in a pulsed manner, and it can be assisted by a fan to extract air, so that The surface temperature of the workpiece can be quickly lowered to a temperature below 700°C and stabilized for a period of time, which promotes the precipitation and spheroidization of carbon atoms in the grains, and then nucleates and grows to form fine carbides in a dispersed distribution.
  • the method of the invention is especially suitable for surface layer strengthening of high-end high-performance carburized gear parts and shaft parts.
  • the present invention designs the alternating times of carburizing cycle and diffusion cycle and the specific duration of each cycle according to the carbon concentration gradient curve required by the workpiece, and precisely controls the carbon concentration gradient curve of the carburizing layer;
  • the forced circulation of pressurized air rapidly cools the surface of the workpiece to below 700°C, so that carbides are uniformly precipitated and the structure is refined. Martensite and retained austenite (grade 1-2) on the surface of the workpiece, with a hardness above 62HRC.
  • the method of the invention has the advantages of short technological process, high carburizing efficiency, cleanness and pollution-free, and strong practicability.
  • Heat treatment technical requirements standard JB/T6141.3-1992 vacuum carburized carburized layer carbide ⁇ 2 grades, surface martensite and retained austenite ⁇ 2 grades, carburized layer 0.9 ⁇ 1.2mm, surface hardness above HRC62 .
  • Carburizing method respectively adopt the traditional vacuum low-pressure carburizing method in the prior art and the variable temperature vacuum carburizing method of the present embodiment provided below.
  • the present embodiment provides a variable temperature vacuum carburizing method for obtaining dispersed fine carbides, including the following stages:
  • Heating and holding stage heat the workpiece to 650°C within 30 minutes, hold it for 60 minutes, then heat it to 960°C required for the subsequent pulse carburizing stage within 30 minutes, and hold it at this temperature for 20 minutes.
  • Pulse carburizing stage At 960°C, 14 carburizing cycles and diffusion cycles were alternated for a total duration of 200 minutes.
  • the carburizing time of the first carburizing cycle was 5.4 minutes and the number of pulses was 3.
  • the second to fourteenth carburizing cycles are 1.8 minutes, and the number of pulses is 1.
  • the second to fourteenth diffusion cycle durations were 2.8 minutes, 4.0 minutes, 5.1 minutes and 6.2 minutes, 7.3 minutes, 8.3 minutes, 9.4 minutes, 10.5 minutes, 11.6 minutes, 12.6 minutes, 13.7 minutes, 14.8 minutes, 15.9 minutes and 50 minutes.
  • the carburizing gas is acetylene, the flow rate of acetylene is 40L/min, and the carburizing pressure is 1000Pa. After the carburizing cycle and the diffusion cycle are all over, the carbon content on the surface of the workpiece is close to the maximum solubility of carbon in austenite at the quenching temperature of the material.
  • Temperature change stage Fill the furnace with 3 ⁇ 10 5 Pa nitrogen and use a fan to force circulation, so that the surface of the workpiece is rapidly cooled to 620°C, kept at this temperature for 10 minutes, then exhausted and vacuumed, and then immediately heated to The quenching temperature is 800°C, and the temperature is kept for 60 minutes for soaking. After changing the temperature, carbon atoms precipitate and spheroidize in the grains, which promotes the formation of fine carbides in a dispersed distribution.
  • Quenching stage fill the furnace with 0.8 ⁇ 10 5 Pa nitrogen gas again and maintain the pressure, cool the workpiece with oil with an oil temperature of 60°C and continue stirring, and perform gas-oil composite quenching to solidify and further refine the grains .
  • the martensite is 4th grade
  • the retained austenite is 4th grade
  • the surface carbide is 4th grade And was reticular.
  • the surface hardness of the test piece is HRC58.5
  • the surface carbon content is 1.5%
  • the effective hardened layer depth is 1.1mm.
  • the martensite is grade 2 and is cryptocrystalline or fine needle-like structure, and the residual austenite
  • the body is grade 1
  • the carbide is grade 1 and dispersedly distributed
  • the carbide size is 200nm to 500nm
  • the shape is mainly spherical.
  • the surface hardness of the test piece is HRC63.7
  • the surface carbon content is 1.2%
  • the effective hardened layer depth is 1.1mm.
  • the vacuum low-pressure carburizing method of the present invention can increase the carbon content of the carburized layer and obtain a fine, well-formed and well-distributed carbide structure, thereby enabling the processed material to obtain better strength and toughness, and improving the strength of the material. service performance.
  • Heat treatment technical requirements standard JB/T6141.3-1992 vacuum carburized carburized layer carbide ⁇ 2 grades, surface martensite and retained austenite ⁇ 2 grades, carburized layer 1.9 ⁇ 2.2mm, surface hardness HRC62 or more .
  • Carburizing method The variable temperature vacuum carburizing method and the vacuum pulse carburizing method without any variable temperature stage provided below are respectively used.
  • the present embodiment provides a variable temperature vacuum carburizing method for obtaining dispersed fine carbides, including the following stages:
  • Heating and holding stage heat the workpiece to 650°C within 30 minutes, hold it for 100 minutes, then heat it to 930°C required for the subsequent pulse carburizing stage within 30 minutes, and hold it at this temperature for 45 minutes.
  • Pulse carburizing stage At 930°C, 18 carburizing cycles and diffusion cycles were alternated, and the total duration was 310 minutes.
  • the duration of the first carburizing cycle in the pulse carburizing stage is 4.5 minutes, and the number of pulses is 3; the second to eighteenth carburizing cycles are 1.5 minutes, and the number of pulses is 1.
  • the carburizing gas is acetylene, the flow rate of acetylene is 40L/min, and the carburizing pressure is 1000Pa.
  • the durations of the first to eighteenth diffusion cycles in this pulse carburizing stage are 3.4 minutes, 5.0 minutes, 6.4 minutes, 7.8 minutes, 9.2 minutes, 10.6 minutes, 12.0 minutes, 13.4 minutes, 14.8 minutes, 16.2 minutes, 17.6 minutes , 19.1 minutes, 20.5 minutes, 21.9 minutes, 23.3 minutes, 24.8 minutes, 26.2 minutes and 27.7 minutes.
  • the carbon content on the surface of the workpiece is close to the maximum solubility of carbon in austenite at the carburizing temperature.
  • the second pulse carburizing stage At 930°C, 15 carburizing cycles and diffusion cycles were alternated for a total duration of 615 minutes.
  • the duration of the first carburizing cycle in the pulse carburizing stage is 3 minutes, and the number of pulses is 2; the second to fifteenth carburizing cycles are 1.5 minutes, and the number of pulses is 1.
  • the carburizing gas is acetylene, the flow rate of acetylene is 40L/min, and the carburizing pressure is 1000Pa.
  • the durations of the first to fifteenth diffusion cycles in the pulse carburizing stage are 5.8 minutes, 10.2 minutes, 14.6 minutes, 19.2 minutes, 23.9 minutes, 28.6 minutes, 33.5 minutes, 38.4 minutes, 43.3 minutes, 48.3 minutes, 53.4 minutes , 58.6 minutes, 64.1 minutes, 70.1 minutes and 79 minutes.
  • Temperature change stage Fill the furnace with 3 ⁇ 10 5 Pa nitrogen and use a fan to force the circulation, so that the surface of the workpiece is rapidly cooled to 620°C within 5 minutes, kept at this temperature for 15 minutes, and then exhausted and evacuated. Then immediately raise the temperature to the quenching temperature of 850°C, and keep the temperature for 45 minutes to soak.
  • Quenching stage fill the furnace with 0.8 ⁇ 10 5 Pa nitrogen again and maintain the pressure, cool the workpiece with oil at 60°C and continue to stir, and perform gas-oil composite quenching to solidify and further refine the grains .
  • an intermediate temperature change stage and a second pulse carburizing stage are added between the temperature change stage and the quenching stage.
  • Fig. 6a is a morphology diagram of the fine carbide structure of the gear treated by the variable temperature vacuum carburizing method in this embodiment.
  • the martensite structure is grade 1, and the carbides are grade 1 and spherical in shape and fine in size and diffusely distributed.
  • Figure 6b shows the fine carbide structure morphology of the gear treated by the vacuum pulse carburizing method without any temperature change stage, and the carbide grade is grade 3 (grain block system).
  • Fig. 7 is a hardness-depth distribution curve of the carburized layer of the gear treated by the variable temperature vacuum carburizing method of this embodiment, wherein the carburized layer depth is 2.16mm, and the surface hardness is >820HV.
  • Fig. 8 is the detection result of the contact fatigue strength of the gear treated by the variable temperature vacuum carburizing method of this embodiment, the contact fatigue limit is 1921Mpa, which is 17.3% higher than the contact fatigue limit of the conventional carburizing and quenching gear which is 1638Mpa.
  • the heating process is segmented according to the workpiece material, size and other factors. If segmented, the heating temperature, heating time, and holding time of each segment are determined.
  • the carburizing temperature of the pulse step, the number of carburizing cycles and diffusion cycles in the carburizing stage, the duration of each cycle, and the carburizing cycle can be determined according to the carbon concentration gradient of the workpiece surface and the effective hardened layer depth.
  • the number of pulses determine the gas pressure, temperature change temperature, temperature change duration, quenching temperature, and quenching duration in the variable temperature stage; and determine the specific quenching means in the quenching stage, such as oil temperature in oil quenching, gas-oil composite quenching in Inflation pressure, inflation time, oil temperature.

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Abstract

Disclosed are a temperature-variable vacuum carburizing method for obtaining dispersedly distributed fine carbides, comprising a heating and insulating stage, a pulse carburizing stage, a temperature-variable stage and a quenching stage. The pulse carburizing stage comprises carrying out alternating carburizing periods and diffusion periods multiple times at a carburization temperature, wherein a carburizing gas is filled into a carburizing chamber in a pulsed manner during the carburizing periods. The temperature-variable stage comprises: introducing a cooling gas into the carburizing chamber after the pulse carburizing stage, so that a surface layer of a workpiece is rapidly cooled to a temperature below 700°C and stabilized for a period of time, so that carbides are uniformly precipitated and spheroidized; then pumping to vacuum, immediately heating to a quenching temperature of 750-980°C and maintaining the temperature, and quenching and cooling once the workpiece is completely austenitized. In the present method, the strength and toughness of the material are developed to the greatest extent, thereby improving the service performance of the workpiece.

Description

一种获得弥散分布的细小碳化物的真空渗碳方法A Vacuum Carburizing Method for Obtaining Dispersed Fine Carbide 技术领域technical field
本发明涉及一种真空渗碳热处理技术,尤其涉及一种获得弥散分布的细小碳化物的变温真空渗碳方法。The invention relates to a vacuum carburizing heat treatment technology, in particular to a variable temperature vacuum carburizing method for obtaining dispersed fine carbides.
背景技术Background technique
热处理是通过改变工件内部的显微组织,或改变工件表面的化学成分,赋予或改善工件的服役性能,充分发挥材料潜力的一种工艺技术。热处理是机械制造行业的关键核心技术,随着对热处理技术的不断重视,热处理产业逐渐由粗放型向精细化发展,更加重视新工艺、新技术、提高产品内在质量、节能节材降耗延寿、关注经济效益等。真空低压渗碳技术以少无氧化、节能减排、清洁热处理等优势,逐步替代可控气氛渗碳设备,在关键零部件如齿轮、传动轴等方面应用越来越广泛。Heat treatment is a process technology that gives or improves the service performance of the workpiece by changing the microstructure inside the workpiece, or changing the chemical composition of the workpiece surface, and fully exploits the potential of the material. Heat treatment is a key core technology in the machinery manufacturing industry. With the continuous emphasis on heat treatment technology, the heat treatment industry has gradually developed from extensive to refined, and more attention has been paid to new processes, new technologies, improving product intrinsic quality, saving energy, reducing consumption and prolonging life. Focus on economic benefits, etc. Vacuum low-pressure carburizing technology gradually replaces controllable atmosphere carburizing equipment with the advantages of less oxidation, energy saving and emission reduction, and clean heat treatment. It is more and more widely used in key parts such as gears and transmission shafts.
重载齿轮、轴等关键承载零部件广泛应用于航空航天、风电、高速机车、重载汽车等行业,普遍要求“外硬内韧”,通常采用渗碳淬火方式实现表层强化。研究表明,提高渗碳层的含碳量并获得细小、形态和分布良好的碳化物对热处理工件的强韧性十分有利,表面硬度高达800-1000HV1。Heavy-duty gears, shafts and other key load-bearing parts are widely used in aerospace, wind power, high-speed locomotives, heavy-duty vehicles and other industries. It is generally required to be "hard on the outside and tough on the inside", and the surface layer is usually strengthened by carburizing and quenching. Studies have shown that increasing the carbon content of the carburized layer and obtaining fine, well-formed and well-distributed carbides is very beneficial to the strength and toughness of the heat-treated workpiece, and the surface hardness is as high as 800-1000HV1.
如图1、图3所示,利用当前现有的真空渗碳方法无法实现上述要求,只能在较低含碳量(0.8%以下)时实现对碳化物的尺寸和形态的有效控制,一旦提高渗碳层的含碳量往往出现对产品性能有害的网状碳化物,即碳原子总是在奥氏体晶界处析出,却无法获得在奥氏体晶粒内形核、长大并形成弥散分布的碳化物,难以最大程度发挥材料的强韧性。As shown in Figure 1 and Figure 3, the above requirements cannot be achieved by using the current vacuum carburizing method, and the effective control of the size and shape of carbides can only be achieved at a low carbon content (below 0.8%). Increasing the carbon content of the carburized layer often produces network carbides that are harmful to product performance, that is, carbon atoms are always precipitated at the austenite grain boundaries, but cannot be nucleated, grown and formed in the austenite grains. The formation of diffusely distributed carbides makes it difficult to maximize the strength and toughness of the material.
发明内容Contents of the invention
有鉴于现有技术的上述问题,特此提出本发明。In view of the above-mentioned problems of the prior art, the present invention is hereby proposed.
本发明的一个目的是提供了一种获得弥散分布的细小碳化物的变温真空渗碳方法,在提高渗碳层的含碳量的同时避免产生有害的网状碳化物,从而实现材料的外硬内韧的目标特性。该方法工艺流程短、渗碳效率高、清洁无污染、实用性强。One object of the present invention is to provide a variable temperature vacuum carburizing method for obtaining dispersed fine carbides, which can increase the carbon content of the carburized layer while avoiding harmful network carbides, so as to realize the external hardness of the material. The target characteristic of internal toughness. The method has the advantages of short technological process, high carburizing efficiency, cleanness and pollution-free, and strong practicability.
本发明的目的是通过以下技术方案实现的:The purpose of the present invention is achieved through the following technical solutions:
本发明的获得弥散分布的细小碳化物的变温真空渗碳方法,包括加热保温阶段、脉冲渗碳阶段、变温阶段、淬火阶段;The variable temperature vacuum carburizing method for obtaining dispersed fine carbides of the present invention includes a heating and heat preservation stage, a pulse carburizing stage, a variable temperature stage, and a quenching stage;
所述脉冲渗碳阶段包括在渗碳温度下交替进行多次渗碳周期和扩散周期,其中在所述渗碳周期中渗碳气体以脉冲方式充入渗碳室,工件表层的碳浓度梯度和有效硬化层深度能够通过所述渗碳周期和所述扩散周期交替进行的次数及每次的持续时间进行调整,所述工件表层的含碳量接近所述渗碳温度下碳在奥氏体中的最大溶解度;The pulse carburizing stage includes alternately performing multiple carburizing cycles and diffusion cycles at the carburizing temperature, wherein in the carburizing cycle, the carburizing gas is pulsed into the carburizing chamber, and the carbon concentration gradient of the surface layer of the workpiece and The effective hardened layer depth can be adjusted by the number of alternate carburizing cycles and the diffusion cycle and the duration of each time. The carbon content of the surface layer of the workpiece is close to the carbon in the austenite at the carburizing temperature. the maximum solubility;
所述变温阶段包括:在所述脉冲渗碳阶段后向所述渗碳室充入冷却气体以使所述工件表层快速冷却至700℃以下一温度并稳定一段时间,从而使碳化物均匀析出并球化,随后抽至真空,立即升温至淬火温度750℃至980℃并保温一段时间,从而使工件均热且完全奥氏体化;The temperature changing stage includes: filling the carburizing chamber with cooling gas after the pulse carburizing stage to rapidly cool the surface layer of the workpiece to a temperature below 700°C and stabilize it for a period of time, so that carbides are uniformly precipitated and Spheroidizing, then evacuate to vacuum, immediately raise the temperature to the quenching temperature of 750°C to 980°C and hold it for a period of time, so that the workpiece is evenly heated and completely austenitized;
所述淬火阶段选择以下任一种淬火方式:直接高压气淬、直接油淬、气油复合淬火。In the quenching stage, any one of the following quenching methods is selected: direct high-pressure gas quenching, direct oil quenching, and gas-oil composite quenching.
在本发明的一种可能实现方式中,在所述变温阶段前还包括至少一个中间变温阶段和至少一个第二脉冲渗碳阶段;所述中间变温阶段包括向所述渗碳室充入冷却气体以使工件表层快速冷却至700℃以下一温度并稳定一段时间,从而使碳化物均匀析出并球化,随后抽至真空,立即升温至所述第二脉冲渗碳阶段所需的温度。In a possible implementation of the present invention, at least one intermediate temperature change stage and at least one second pulse carburizing stage are included before the temperature change stage; the intermediate temperature change stage includes filling the carburizing chamber with cooling gas The surface layer of the workpiece is rapidly cooled to a temperature below 700°C and stabilized for a period of time, so that the carbides are uniformly precipitated and spheroidized, and then vacuumed, and the temperature is immediately raised to the temperature required for the second pulse carburizing stage.
在本发明的一种可能实现方式中,所述第二脉冲渗碳阶段中的各个渗碳周期和扩散周期的交替次数和持续时间和所述脉冲渗碳阶段的各个渗碳周期和扩散周期的交替次数和持续时间至少部分不同。In a possible implementation of the present invention, the alternating times and duration of each carburizing period and diffusion period in the second pulse carburizing stage and the respective carburizing periods and diffusion periods in the pulse carburizing stage The number and duration of the alternations are at least partially different.
在本发明的一种可能实现方式中,在所述脉冲渗碳阶段中,所述渗碳温度为750至980℃,渗碳压力为800至1500Pa,所述渗碳周期的总时间和所述扩散周期的总时间的比率为1:2至1:7。In a possible implementation of the present invention, in the pulse carburizing stage, the carburizing temperature is 750 to 980°C, the carburizing pressure is 800 to 1500Pa, the total time of the carburizing cycle and the The ratio of the total time of the diffusion cycle is 1:2 to 1:7.
在本发明的一种可能实现方式中,在所述变温阶段中,所述冷却气体的压力≥2×10 5Pa,降温至温度700℃以下后的保温时长为5至60分钟,升温至淬火温度750℃至980℃后的保温时长为5至120分钟。 In a possible implementation of the present invention, in the temperature changing stage, the pressure of the cooling gas is ≥2×10 5 Pa, and the holding time after cooling down to a temperature below 700°C is 5 to 60 minutes. The holding time after the temperature is 750°C to 980°C is 5 to 120 minutes.
在本发明一种可能实现方式中,所述渗碳气体为乙炔或丙烷,所述冷却气体为氮气、氩气或氦气。In a possible implementation manner of the present invention, the carburizing gas is acetylene or propane, and the cooling gas is nitrogen, argon or helium.
在本发明一种可能实现方式中,所述脉冲渗碳阶段的持续时间≥30分钟。In a possible implementation manner of the present invention, the duration of the pulse carburizing stage is ≥30 minutes.
在本发明一种可能实现方式中,所述脉冲渗碳阶段的持续时间≥120分钟。In a possible implementation manner of the present invention, the duration of the pulse carburizing stage is ≥120 minutes.
与现有技术相比,本发明所提供的获得弥散分布的细小碳化物的变温真空渗碳方 法,在脉冲渗碳阶段通过采用交替多次的渗碳周期和扩散周期并调整它们的周期数和周期时间,获得所需的碳浓度梯度曲线;在变温阶段通过加压充气使工件表层快速冷却从而均匀析出碳化物并细化组织。由此,在提高被处理构件的渗碳层的含碳量的同时避免产生有害的网状碳化物,使被处理构件获得弥散分布的细小碳化物,从而实现被处理构件的外硬内韧的目标特性。该方法工艺流程短、渗碳效率高、清洁无污染、实用性强,使经处理的材料获得更好的强韧性,提高了材料的服役性能。Compared with the prior art, the variable temperature vacuum carburizing method for obtaining dispersed fine carbides provided by the present invention adopts alternate carburizing cycles and diffusion cycles in the pulse carburizing stage and adjusts their cycle numbers and Cycle time, to obtain the required carbon concentration gradient curve; in the variable temperature stage, the surface layer of the workpiece is rapidly cooled by pressurized air to uniformly precipitate carbides and refine the structure. Thus, while increasing the carbon content of the carburized layer of the treated member, avoiding the generation of harmful network carbides, the treated member can obtain dispersed fine carbides, so as to realize the principle of the treated member being hard on the outside and tough on the inside. target properties. The method has the advantages of short technological process, high carburizing efficiency, cleanness and no pollution, and strong practicability, so that the treated material can obtain better strength and toughness, and the service performance of the material is improved.
附图说明Description of drawings
附图中采用示意性显示,其中主要特性及效应被部分地显著放大展示,用以阐释功能、作用原理、技术方案及特征。因此,在附图中示出的曲线图的尺寸及比例在此并非一定按比例绘示,也不代表具体数值。在可实施的许多实施方式中,尺寸及比例等可能有别于此处的图示。Schematic representations are used in the drawings, in which some of the main features and effects are significantly enlarged to illustrate functions, principles of action, technical solutions and features. Therefore, the dimensions and proportions of the graphs shown in the accompanying drawings are not necessarily drawn to scale, nor represent specific numerical values. In many embodiments that can be implemented, the dimensions, proportions, etc. may be different from those shown here.
图1为现有技术中真空低压渗碳传统工艺曲线示意图;Fig. 1 is a schematic diagram of the traditional process curve of vacuum low-pressure carburizing in the prior art;
图2为本发明一个实施例的变温真空渗碳方法的温度、压力随时间变化的曲线示意图;Fig. 2 is the schematic diagram of the curve of temperature and pressure changing with time of the variable temperature vacuum carburizing method of an embodiment of the present invention;
图3为经过现有技术中传统真空低压渗碳方法处理的轴的表面碳化物组织形貌图,放大倍数为500;Fig. 3 is the topography diagram of the carbide structure on the surface of the shaft treated by the traditional vacuum low-pressure carburizing method in the prior art, with a magnification of 500;
图4a为经过本发明一实施例的变温真空渗碳方法处理的轴的表面碳化物组织形貌图,放大倍数为500;Figure 4a is a topography diagram of carbides on the surface of the shaft treated by the variable temperature vacuum carburizing method according to an embodiment of the present invention, with a magnification of 500;
图4b为经过本发明一实施例的变温真空渗碳方法处理的轴的SEM球状碳化物组织形貌图;Fig. 4b is a SEM spherical carbide microstructure diagram of a shaft treated by a variable temperature vacuum carburizing method according to an embodiment of the present invention;
图5为本发明另一实施例的变温真空渗碳方法的温度、压力随时间变化的曲线示意图;Fig. 5 is a schematic diagram of curves of temperature and pressure changing with time in a variable temperature vacuum carburizing method according to another embodiment of the present invention;
图6a为经过本发明另一实施例的变温真空渗碳方法处理的齿轮的细小碳化物组织形貌图,放大倍数为500;Fig. 6a is a fine carbide structure topography diagram of a gear treated by a variable temperature vacuum carburizing method according to another embodiment of the present invention, with a magnification of 500;
图6b为经过不含任何变温阶段的真空脉冲渗碳方法处理的齿轮的细小碳化物组织形貌图,放大倍数为500;Fig. 6b is a fine carbide microstructure diagram of the gear treated by the vacuum pulse carburizing method without any variable temperature stage, with a magnification of 500;
图7为经过本发明另一实施例的变温真空渗碳方法处理的齿轮的渗碳层的硬度-深度分布曲线图;Fig. 7 is the hardness-depth distribution curve of the carburized layer of the gear treated by the variable temperature vacuum carburizing method according to another embodiment of the present invention;
图8为经过本发明另一实施例的变温真空渗碳方法处理的齿轮的接触疲劳损伤累积曲 线。Fig. 8 is the contact fatigue damage accumulation curve of the gear treated by the variable temperature vacuum carburizing method according to another embodiment of the present invention.
具体实施方式Detailed ways
下面结合本发明实施例中的附图,对本发明实施例中的技术方案进行清楚、完整地描述;显然,所描述的实施例仅仅是本发明一部分实施例,而不是全部的实施例,这并不构成对本发明的限制。基于本发明的实施例,本领域普通技术人员在没有做出创造性劳动前提下所获得的所有其他实施例,都属于本发明的保护范围。The technical solutions in the embodiments of the present invention are clearly and completely described below in conjunction with the accompanying drawings in the embodiments of the present invention; obviously, the described embodiments are only some of the embodiments of the present invention, not all of them, and this does not mean It does not constitute a limitation of the present invention. Based on the embodiments of the present invention, all other embodiments obtained by persons of ordinary skill in the art without making creative efforts belong to the protection scope of the present invention.
首先对本文中可能使用的术语进行如下说明:First, the terms that may be used in this article are explained as follows:
术语“和/或”是表示两者任一或两者同时均可实现,例如,X和/或Y表示既包括“X”或“Y”的情况也包括“X和Y”的三种情况。The term "and/or" means that either or both can be realized at the same time, for example, X and/or Y means that both "X" or "Y" and "X and Y" are included .
术语“包括”、“包含”、“含有”、“具有”或其它类似语义的描述,应被解释为非排它性的包括。例如:包括某技术特征要素(如原料、组分、成分、载体、剂型、材料、尺寸、零件、部件、机构、装置、步骤、工序、方法、反应条件、加工条件、参数、算法、信号、数据、产品或制品等),应被解释为不仅包括明确列出的某技术特征要素,还可以包括未明确列出的本领域公知的其它技术特征要素。The terms "comprising", "comprising", "containing", "having" or other descriptions with similar meanings shall be construed as non-exclusive inclusions. For example: including certain technical feature elements (such as raw materials, components, ingredients, carriers, dosage forms, materials, dimensions, parts, components, mechanisms, devices, steps, procedures, methods, reaction conditions, processing conditions, parameters, algorithms, signals, data, products or products, etc.), should be interpreted as including not only a certain technical feature element explicitly listed, but also other technical feature elements not explicitly listed in the art.
术语“由……组成”表示排除任何未明确列出的技术特征要素。若将该术语用于权利要求中,则该术语将使权利要求成为封闭式,使其不包含除明确列出的技术特征要素以外的技术特征要素,但与其相关的常规杂质除外。如果该术语只是出现在权利要求的某子句中,那么其仅限定在该子句中明确列出的要素,其他子句中所记载的要素并不被排除在整体权利要求之外。The term "consisting of" means excluding any technical characteristic elements not explicitly listed. If this term is used in a claim, the term will make the claim closed so that it does not contain technical characteristic elements other than those expressly listed, except for conventional impurities related to them. If the term only appears in a certain clause of a claim, it only limits the elements explicitly listed in the clause, and the elements stated in other clauses are not excluded from the entire claim.
除另有明确的规定或限定外,术语“安装”、“相连”、“连接”、“固定”等术语应做广义理解,例如:可以是固定连接,也可以是可拆卸连接,或一体地连接;可以是机械连接,也可以是电连接;可以是直接相连,也可以通过中间媒介间接相连,可以是两个元件内部的连通。对于本领域的普通技术人员而言,可以根据具体情况理解上述术语在本文中的具体含义。Unless otherwise expressly stipulated or limited, terms such as "mounted", "connected", "connected" and "fixed" should be interpreted in a broad sense, for example: it can be a fixed connection or a detachable connection, or an integral Connection; it can be a mechanical connection or an electrical connection; it can be a direct connection or an indirect connection through an intermediary, and it can be the internal communication of two components. Those of ordinary skill in the art can understand the specific meanings of the above terms herein according to specific situations.
当浓度、温度、压力、尺寸或者其它参数以数值范围形式表示时,该数值范围应被理解为具体公开了该数值范围内任何上限值、下限值、优选值的配对所形成的所有范围,而不论该范围是否被明确记载;例如,如果记载了数值范围“2~8”时,那么该数值范围应被解释为包括“2~7”、“2~6”、“5~7”、“3~4和6~7”、“3~5和7”、“2和5~7”等范围。除另有说明外,本文中记载的数值范围既包括其端值也包括在该数值范围内的所有 整数和分数。When the concentration, temperature, pressure, size or other parameters are expressed in the form of numerical ranges, the numerical ranges should be understood as specifically disclosing all the ranges formed by the pairing of any upper limit, lower limit and preferred value within the numerical range , regardless of whether the range is explicitly stated; for example, if the numerical range "2-8" is stated, then the numerical range should be interpreted as including "2-7", "2-6", "5-7" , "3~4 and 6~7", "3~5 and 7", "2 and 5~7" and other ranges. Unless otherwise indicated, numerical ranges recited herein include their endpoints and all integers and fractions subsumed within the numerical range.
术语“中心”、“纵向”、“横向”、“长度”、“宽度”、“厚度”、“上”、“下”、“前”、“后”、“左”、“右”、“竖直”、“水平”、“顶”、“底”“内”、“外”、“顺时针”、“逆时针”等指示的方位或位置关系为基于附图所示的方位或位置关系,仅是为了便于描述和简化描述,而不是明示或暗示所指的装置或元件必须具有特定的方位、以特定的方位构造和操作,因此不能理解为对本文的限制。The terms "center", "longitudinal", "transverse", "length", "width", "thickness", "top", "bottom", "front", "rear", "left", "right", " The orientation or positional relationship indicated by "vertical", "horizontal", "top", "bottom", "inner", "outer", "clockwise", "counterclockwise", etc. is based on the orientation or positional relationship shown in the drawings , is only for convenience and simplification of description, but does not express or imply that the device or element referred to must have a specific orientation, be constructed and operated in a specific orientation, and thus should not be construed as a limitation on this document.
本发明实施例中未作详细描述的内容属于本领域专业技术人员公知的现有技术。本发明实施例中未注明具体条件者,按照本领域常规条件或制造商建议的条件进行。本发明实施例中所用试剂或仪器未注明生产厂商者,均为可以通过市售购买获得的常规产品。The content not described in detail in the embodiments of the present invention belongs to the prior art known to those skilled in the art. In the embodiment of the present invention, if no specific conditions are indicated, it is carried out according to the conventional conditions in the art or the conditions suggested by the manufacturer. The reagents or instruments used in the examples of the present invention, whose manufacturers are not indicated, are all conventional products that can be purchased from the market.
本发明的获得弥散分布的细小碳化物的变温真空渗碳方法,包括加热保温阶段、脉冲渗碳阶段、变温阶段、淬火阶段;The variable temperature vacuum carburizing method for obtaining dispersed fine carbides of the present invention includes a heating and heat preservation stage, a pulse carburizing stage, a variable temperature stage, and a quenching stage;
所述脉冲渗碳阶段包括交替多次的渗碳周期和扩散周期,其中在渗碳周期中渗碳气体以脉冲方式充入渗碳室,工件表层的碳浓度梯度和有效硬化层深度能够通过所述渗碳周期和所述扩散周期交替进行的次数及每次的持续时间进行调整;在一些实施方式中,在经过所述脉冲渗碳阶段后,材料表面含碳量接近该渗碳温度下碳在奥氏体中的最大溶解度;The pulse carburizing stage includes alternate carburizing cycles and diffusion cycles, wherein carburizing gas is pulsed into the carburizing chamber during the carburizing cycle, and the carbon concentration gradient and effective hardened layer depth on the surface of the workpiece can pass through the carburizing cycle. The number of times the carburizing cycle and the diffusion cycle are alternated and the duration of each time are adjusted; in some embodiments, after the pulse carburizing stage, the carbon content on the surface of the material is close to the carbon at the carburizing temperature Maximum solubility in austenite;
所述变温阶段包括:向所述渗碳室充入冷却气体以使工件表层快速冷却至700℃以下一温度,即Acl线以下温度,并稳定一段时间,从而使碳化物均匀析出并球化,随后抽至真空,立即升温至淬火温度750℃-980℃,即Ac3或Ac1线以上30-50℃,并保温一段时间,从而使工件均热且完全奥氏体化;The temperature changing stage includes: filling the carburizing chamber with cooling gas to quickly cool the surface of the workpiece to a temperature below 700°C, that is, the temperature below the Acl line, and stabilize it for a period of time, so that the carbides are uniformly precipitated and spheroidized. Then evacuate to a vacuum, immediately raise the temperature to the quenching temperature of 750°C-980°C, that is, 30-50°C above the Ac3 or Ac1 line, and keep it warm for a period of time, so that the workpiece is evenly heated and completely austenitized;
所述淬火阶段选择以下任一种淬火方式:直接高压气淬、直接油淬、气油淬。In the quenching stage, any one of the following quenching methods is selected: direct high-pressure gas quenching, direct oil quenching, and gas-oil quenching.
在所述加热保温阶段中,可以根据工件材质及尺寸确定加热过程是否分段,设定各段的加热温度、加热时间、保温时间。在编制加热曲线后,将工件放于真空炉抽真空,根据加热曲线进行加热。In the heating and heat preservation stage, it can be determined whether the heating process is segmented according to the material and size of the workpiece, and the heating temperature, heating time, and heat preservation time of each segment can be set. After the heating curve is compiled, the workpiece is placed in a vacuum furnace to evacuate and heated according to the heating curve.
在所述脉冲渗碳阶段中,渗碳温度为750至980℃,渗碳压力为800至1500Pa,渗碳周期和扩散周期交替进行的次数及每次的持续时间根据所需的有效硬化层深度或碳浓度梯度曲线确定,渗碳周期总时间和扩散周期总时间的比率为1:2至1:7,表面含碳量数值可以设定为0.8%至2.0%,优选为0.8%至1.3%。In the pulse carburizing stage, the carburizing temperature is 750 to 980°C, and the carburizing pressure is 800 to 1500Pa. The number of carburizing cycles and diffusion cycles and the duration of each cycle are based on the required effective hardened layer depth. Or determined by the carbon concentration gradient curve, the ratio of the total time of the carburizing cycle to the total time of the diffusion cycle is 1:2 to 1:7, and the value of the surface carbon content can be set at 0.8% to 2.0%, preferably 0.8% to 1.3% .
在所述脉冲渗碳阶段中,选择乙炔或丙烷气氛为渗碳气体。In the pulse carburizing stage, acetylene or propane atmosphere is selected as the carburizing gas.
所述脉冲渗碳阶段的持续时间≥30分钟。在一些实施方式中,所述脉冲渗碳阶段的持续时间≥120分钟。The duration of the pulse carburizing phase is ≥30 minutes. In some embodiments, the duration of the pulse carburizing phase is > 120 minutes.
在所述变温阶段中,在所述渗碳室充入冷却气体的压力≥2×10 5Pa,降温至温度700℃以下后保温5至60分钟,升温至淬火温度750℃至980℃后保温5至120分钟。 In the temperature changing stage, the carburizing chamber is filled with cooling gas with a pressure ≥ 2×10 5 Pa, the temperature is lowered to below 700°C and then kept for 5 to 60 minutes, and the temperature is raised to the quenching temperature of 750°C to 980°C and then kept for heat preservation 5 to 120 minutes.
在所述变温阶段中,充入所述渗碳室的气体选择氮气、氩气或氦气。In the temperature changing stage, nitrogen, argon or helium is selected as the gas filled into the carburizing chamber.
本发明中:In the present invention:
在所述脉冲渗碳阶段中,在真空条件下通入乙炔或丙烷气氛,高温使活性碳原子在材料固体中扩散并形成碳化物,冷却后实现材料表面硬化的目的。脉冲渗碳阶段非常关键,渗碳周期和扩散周期的持续时间和交替次数直接影响着材料表层的碳浓度梯度曲线,进而影响着材料的显微组织及性能,渗碳温度的高低以及总渗碳时间的长短决定了奥氏体晶粒是否会长大。In the pulse carburizing stage, an acetylene or propane atmosphere is introduced under vacuum conditions, and the high temperature causes active carbon atoms to diffuse in the solid material and form carbides, and the surface hardening of the material is achieved after cooling. The pulse carburizing stage is very critical. The duration and alternating times of the carburizing cycle and the diffusion cycle directly affect the carbon concentration gradient curve on the surface of the material, which in turn affects the microstructure and properties of the material, the carburizing temperature and the total carburizing The length of time determines whether the austenite grains will grow.
在脉冲渗碳结束后的所述变温阶段中,使工件继续留在真空所述渗碳室内,停止加热,以脉冲方式充入氮气、氩气或者氦气,并且可以辅以风机抽气,使得工件表面温度能够快速降低至700℃以下一温度并稳定一段时间,促使碳原子在晶粒中析出并球化,进而形核、长大,促使形成弥散分布的细小碳化物。In the temperature-changing stage after the end of pulse carburizing, the workpiece remains in the vacuum carburizing chamber, the heating is stopped, and nitrogen, argon or helium is charged in a pulsed manner, and it can be assisted by a fan to extract air, so that The surface temperature of the workpiece can be quickly lowered to a temperature below 700°C and stabilized for a period of time, which promotes the precipitation and spheroidization of carbon atoms in the grains, and then nucleates and grows to form fine carbides in a dispersed distribution.
本发明的方法尤其适用于高端高性能的渗碳齿轮件、轴类件的表层强化。The method of the invention is especially suitable for surface layer strengthening of high-end high-performance carburized gear parts and shaft parts.
与现有技术相比,本发明的有益效果是:Compared with prior art, the beneficial effect of the present invention is:
本发明在脉冲渗碳阶段根据工件所需的碳浓度梯度曲线设计渗碳周期和扩散周期交替的次数及各个周期具体的持续时间,精确控制渗碳层的碳浓度梯度曲线;在变温阶段依靠加压充气的强制循环,使工件表层快速冷却至700℃以下,从而均匀析出碳化物并细化组织。工件表面马氏体及残余奥氏体(1~2级),硬度62HRC以上。本发明方法具有工艺流程短、渗碳效率高、清洁无污染、实用性强的优点。In the pulse carburizing stage, the present invention designs the alternating times of carburizing cycle and diffusion cycle and the specific duration of each cycle according to the carbon concentration gradient curve required by the workpiece, and precisely controls the carbon concentration gradient curve of the carburizing layer; The forced circulation of pressurized air rapidly cools the surface of the workpiece to below 700°C, so that carbides are uniformly precipitated and the structure is refined. Martensite and retained austenite (grade 1-2) on the surface of the workpiece, with a hardness above 62HRC. The method of the invention has the advantages of short technological process, high carburizing efficiency, cleanness and pollution-free, and strong practicability.
为了更加清晰地展现出本发明所提供的技术方案及所产生的技术效果,下面以具体实施例对本发明实施例所提供的进行详细描述。In order to more clearly demonstrate the technical solutions provided by the present invention and the technical effects produced, the following will describe in detail the embodiments of the present invention provided by specific examples.
实施例1-轴Example 1 - Shaft
尺寸(mm):轴直径φ38,长度150mmDimensions (mm): shaft diameter φ38, length 150mm
材料:18CrNiMo7-6。Material: 18CrNiMo7-6.
热处理技术要求:标准JB/T6141.3-1992真空渗碳后渗碳层碳化物≤2级、表面马氏体及残留奥氏体≤2级、渗碳层0.9~1.2mm、表面硬度HRC62以上。Heat treatment technical requirements: standard JB/T6141.3-1992 vacuum carburized carburized layer carbide ≤ 2 grades, surface martensite and retained austenite ≤ 2 grades, carburized layer 0.9 ~ 1.2mm, surface hardness above HRC62 .
渗碳方法:分别采用现有技术中传统真空低压渗碳方法与以下提供的本实施例的变 温真空渗碳方法。Carburizing method: respectively adopt the traditional vacuum low-pressure carburizing method in the prior art and the variable temperature vacuum carburizing method of the present embodiment provided below.
参阅图2,本实施例提供一种获得弥散分布的细小碳化物的变温真空渗碳方法,包括以下阶段:Referring to Fig. 2, the present embodiment provides a variable temperature vacuum carburizing method for obtaining dispersed fine carbides, including the following stages:
(1)加热保温阶段:在30分钟内将工件加热至650℃,保温60分钟,然后在30分钟分钟内加热至后续脉冲渗碳阶段所需的960℃,在该温度下保温20分钟。(1) Heating and holding stage: heat the workpiece to 650°C within 30 minutes, hold it for 60 minutes, then heat it to 960°C required for the subsequent pulse carburizing stage within 30 minutes, and hold it at this temperature for 20 minutes.
(2)脉冲渗碳阶段:在960℃下,交替14个渗碳周期和扩散周期,持续总时间为200分钟。第一个渗碳周期的渗碳时间为5.4分钟,脉冲次数为3。第二至第十四渗碳周期为1.8分钟,脉冲次数为1。第二至第十四扩散周期持续时间分别为2.8分钟、4.0分钟、5.1分钟和6.2分钟、7.3分钟、8.3分钟、9.4分钟、10.5分钟、11.6分钟、12.6分钟、13.7分钟、14.8分钟、15.9分钟和50分钟。渗碳气体为乙炔,乙炔流量为40L/分钟,渗碳压力为1000Pa。渗碳周期和扩散周期全部结束后,工件表面含碳量接近该材料淬火温度下碳在奥氏体中的最大溶解度。(2) Pulse carburizing stage: At 960°C, 14 carburizing cycles and diffusion cycles were alternated for a total duration of 200 minutes. The carburizing time of the first carburizing cycle was 5.4 minutes and the number of pulses was 3. The second to fourteenth carburizing cycles are 1.8 minutes, and the number of pulses is 1. The second to fourteenth diffusion cycle durations were 2.8 minutes, 4.0 minutes, 5.1 minutes and 6.2 minutes, 7.3 minutes, 8.3 minutes, 9.4 minutes, 10.5 minutes, 11.6 minutes, 12.6 minutes, 13.7 minutes, 14.8 minutes, 15.9 minutes and 50 minutes. The carburizing gas is acetylene, the flow rate of acetylene is 40L/min, and the carburizing pressure is 1000Pa. After the carburizing cycle and the diffusion cycle are all over, the carbon content on the surface of the workpiece is close to the maximum solubility of carbon in austenite at the quenching temperature of the material.
(3)变温阶段:向炉中充入3×10 5Pa氮气并使用风机强制循环,使工件表面快速冷却至620℃,在该温度下保温10分钟,随后排气抽真空,然后立即升温至淬火温度800℃,保温60分钟均热。变温后,碳原子在晶粒中析出并球化,促使形成弥散分布的细小碳化物。 (3) Temperature change stage: Fill the furnace with 3×10 5 Pa nitrogen and use a fan to force circulation, so that the surface of the workpiece is rapidly cooled to 620°C, kept at this temperature for 10 minutes, then exhausted and vacuumed, and then immediately heated to The quenching temperature is 800°C, and the temperature is kept for 60 minutes for soaking. After changing the temperature, carbon atoms precipitate and spheroidize in the grains, which promotes the formation of fine carbides in a dispersed distribution.
(4)淬火阶段:再次向炉中充入0.8×10 5Pa氮气并保持该气压,用油温为60℃油冷却工件并持续搅拌,进行气油复合淬火,以固化、进一步细化晶粒。 (4) Quenching stage: fill the furnace with 0.8×10 5 Pa nitrogen gas again and maintain the pressure, cool the workpiece with oil with an oil temperature of 60°C and continue stirring, and perform gas-oil composite quenching to solidify and further refine the grains .
如图3所示,在经过现有技术中传统真空低压渗碳方法处理后的试件的显微组织中,马氏体为4级,残余奥氏体为4级,表面碳化物为4级且呈网状。试件的表面硬度HRC58.5,表面碳含量1.5%,有效硬化层深度1.1mm。这表明,在现有技术中传统真空低压渗碳方法中,表面往往形成网状碳化物这一有害组织,近表层则常常出现残余奥氏体过多且马氏体粗大的现象,难以满足高端高性能渗碳齿轮件、轴类件的表层强化要求。As shown in Figure 3, in the microstructure of the specimen treated by the traditional vacuum low-pressure carburizing method in the prior art, the martensite is 4th grade, the retained austenite is 4th grade, and the surface carbide is 4th grade And was reticular. The surface hardness of the test piece is HRC58.5, the surface carbon content is 1.5%, and the effective hardened layer depth is 1.1mm. This shows that in the traditional vacuum low-pressure carburizing method in the prior art, the harmful structure of network carbide is often formed on the surface, and the phenomenon of excessive residual austenite and coarse martensite often appears in the near surface layer, which is difficult to meet the high-end requirements. Surface strengthening requirements for high-performance carburized gear parts and shaft parts.
如图4a和图4b所示,在经过实施例1的变温真空渗碳方法处理后的试件的显微组织中,马氏体为2级且呈隐晶或细针状组织,残余奥氏体为1级,碳化物为1级且弥散分布,碳化物尺寸为200nm至500nm,形态以球状为主。试件的表面硬度HRC63.7,表面碳含量1.2%,有效硬化层深度1.1mm。这表明,本发明的真空低压渗碳方法可提高渗碳层的含碳量并获得细小、形态和分布良好的碳化物组织,从而使经处理的材料获得更好的强韧性,提高了材料的服役性能。As shown in Figure 4a and Figure 4b, in the microstructure of the specimen treated by the variable temperature vacuum carburizing method in Example 1, the martensite is grade 2 and is cryptocrystalline or fine needle-like structure, and the residual austenite The body is grade 1, the carbide is grade 1 and dispersedly distributed, the carbide size is 200nm to 500nm, and the shape is mainly spherical. The surface hardness of the test piece is HRC63.7, the surface carbon content is 1.2%, and the effective hardened layer depth is 1.1mm. This shows that the vacuum low-pressure carburizing method of the present invention can increase the carbon content of the carburized layer and obtain a fine, well-formed and well-distributed carbide structure, thereby enabling the processed material to obtain better strength and toughness, and improving the strength of the material. service performance.
实施例2–齿轮Example 2 – Gears
尺寸(mm):
Figure PCTCN2022117851-appb-000001
169×75,模数6.5,齿数24
Dimensions(mm):
Figure PCTCN2022117851-appb-000001
169×75, module 6.5, number of teeth 24
材料:18CrNiMo7-6。Material: 18CrNiMo7-6.
热处理技术要求:标准JB/T6141.3-1992真空渗碳后渗碳层碳化物≤2级、表面马氏体及残留奥氏体≤2级、渗碳层1.9~2.2mm、表面硬度HRC62以上。Heat treatment technical requirements: standard JB/T6141.3-1992 vacuum carburized carburized layer carbide ≤ 2 grades, surface martensite and retained austenite ≤ 2 grades, carburized layer 1.9 ~ 2.2mm, surface hardness HRC62 or more .
渗碳方法:分别采用以下提供的本实施例的变温真空渗碳方法和不含任何变温阶段的真空脉冲渗碳方法。Carburizing method: The variable temperature vacuum carburizing method and the vacuum pulse carburizing method without any variable temperature stage provided below are respectively used.
参阅图5,本实施例提供一种获得弥散分布的细小碳化物的变温真空渗碳方法,包括以下阶段:Referring to Fig. 5, the present embodiment provides a variable temperature vacuum carburizing method for obtaining dispersed fine carbides, including the following stages:
(1)加热保温阶段:在30分钟内将工件加热至650℃,保温100分钟,然后在30分钟内加热至后续脉冲渗碳阶段所需的930℃,在该温度下保温45分钟。(1) Heating and holding stage: heat the workpiece to 650°C within 30 minutes, hold it for 100 minutes, then heat it to 930°C required for the subsequent pulse carburizing stage within 30 minutes, and hold it at this temperature for 45 minutes.
(2)脉冲渗碳阶段:在930℃下,交替18个渗碳周期和扩散周期,持续总时间为310分钟。该脉冲渗碳阶段的第一个渗碳周期的持续时间为4.5分钟,脉冲次数为3;第二至第十八渗碳周期为1.5分钟,脉冲次数为1。渗碳气体为乙炔,乙炔流量为40L/分钟,渗碳压力为1000Pa。该脉冲渗碳阶段的第一至第十八扩散周期持续时间分别为3.4分钟、5.0分钟、6.4分钟、7.8分钟、9.2分钟、10.6分钟、12.0分钟、13.4分钟、14.8分钟、16.2分钟、17.6分钟、19.1分钟、20.5分钟、21.9分钟、23.3分钟、24.8分钟、26.2分钟和27.7分钟。渗碳周期和扩散周期全部结束后,工件表面含碳量接近该渗碳温度下碳在奥氏体中的最大溶解度。(2) Pulse carburizing stage: At 930°C, 18 carburizing cycles and diffusion cycles were alternated, and the total duration was 310 minutes. The duration of the first carburizing cycle in the pulse carburizing stage is 4.5 minutes, and the number of pulses is 3; the second to eighteenth carburizing cycles are 1.5 minutes, and the number of pulses is 1. The carburizing gas is acetylene, the flow rate of acetylene is 40L/min, and the carburizing pressure is 1000Pa. The durations of the first to eighteenth diffusion cycles in this pulse carburizing stage are 3.4 minutes, 5.0 minutes, 6.4 minutes, 7.8 minutes, 9.2 minutes, 10.6 minutes, 12.0 minutes, 13.4 minutes, 14.8 minutes, 16.2 minutes, 17.6 minutes , 19.1 minutes, 20.5 minutes, 21.9 minutes, 23.3 minutes, 24.8 minutes, 26.2 minutes and 27.7 minutes. After the carburizing cycle and the diffusion cycle are all over, the carbon content on the surface of the workpiece is close to the maximum solubility of carbon in austenite at the carburizing temperature.
(3)中间变温阶段:向炉中充入3×10 5Pa氮气并使用风机强制循环,使工件表面快速冷却至620℃,在该温度下保温15分钟,随后排气抽真空,然后立即在15分钟内升温至后续脉冲渗碳阶段所需的930℃变温后,碳原子在晶粒中析出并球化,促使形成弥散分布的细小碳化物。 (3) Intermediate temperature change stage: Fill the furnace with 3×10 5 Pa nitrogen and use a fan to force circulation, so that the surface of the workpiece is rapidly cooled to 620°C, and kept at this temperature for 15 minutes, then exhausted and vacuumed, and then immediately in the After the temperature is raised to 930 °C required for the subsequent pulse carburizing stage within 15 minutes, carbon atoms are precipitated and spheroidized in the grains, which promotes the formation of fine carbides in a dispersed distribution.
(4)第二脉冲渗碳阶段:在930℃下,交替15个渗碳周期和扩散周期,持续总时间为615分钟。该脉冲渗碳阶段的第一个渗碳周期的持续时间为3分钟,脉冲次数为2;第二至第十五渗碳周期为1.5分钟,脉冲次数为1。渗碳气体为乙炔,乙炔流量为40L/分钟,渗碳压力为1000Pa。该脉冲渗碳阶段的第一至第十五扩散周期持续时间分别为5.8分钟、10.2分钟、14.6分钟、19.2分钟、23.9分钟、28.6分钟、33.5分钟、38.4分钟、43.3分钟、48.3分钟、53.4分钟、58.6分钟、64.1分钟、70.1分钟和79分钟。(4) The second pulse carburizing stage: At 930°C, 15 carburizing cycles and diffusion cycles were alternated for a total duration of 615 minutes. The duration of the first carburizing cycle in the pulse carburizing stage is 3 minutes, and the number of pulses is 2; the second to fifteenth carburizing cycles are 1.5 minutes, and the number of pulses is 1. The carburizing gas is acetylene, the flow rate of acetylene is 40L/min, and the carburizing pressure is 1000Pa. The durations of the first to fifteenth diffusion cycles in the pulse carburizing stage are 5.8 minutes, 10.2 minutes, 14.6 minutes, 19.2 minutes, 23.9 minutes, 28.6 minutes, 33.5 minutes, 38.4 minutes, 43.3 minutes, 48.3 minutes, 53.4 minutes , 58.6 minutes, 64.1 minutes, 70.1 minutes and 79 minutes.
(5)变温阶段:向炉中充入3×10 5Pa氮气并使用风机强制循环,使工件表面在5分钟内快速冷却至620℃,在该温度下保温15分钟,随后排气抽真空,然后立即升温至淬火温度850℃,保温45分钟均热。 (5) Temperature change stage: Fill the furnace with 3×10 5 Pa nitrogen and use a fan to force the circulation, so that the surface of the workpiece is rapidly cooled to 620°C within 5 minutes, kept at this temperature for 15 minutes, and then exhausted and evacuated. Then immediately raise the temperature to the quenching temperature of 850°C, and keep the temperature for 45 minutes to soak.
(6)淬火阶段:再次向炉中充入0.8×10 5Pa氮气并保持该气压,用油温为60℃油冷却工件并持续搅拌,进行气油复合淬火,以固化、进一步细化晶粒。 (6) Quenching stage: fill the furnace with 0.8×10 5 Pa nitrogen again and maintain the pressure, cool the workpiece with oil at 60°C and continue to stir, and perform gas-oil composite quenching to solidify and further refine the grains .
在本实施例中,为增加渗碳层厚度,在变温阶段与淬火阶段之间增加了一个中间变温阶段和一个第二脉冲渗碳阶段。In this embodiment, in order to increase the thickness of the carburized layer, an intermediate temperature change stage and a second pulse carburizing stage are added between the temperature change stage and the quenching stage.
图6a为经过本实施例变温真空渗碳方法处理的齿轮的细小碳化物组织形貌图,马氏体组织为1级,碳化物为1级且呈球形、尺寸细小弥散分布。Fig. 6a is a morphology diagram of the fine carbide structure of the gear treated by the variable temperature vacuum carburizing method in this embodiment. The martensite structure is grade 1, and the carbides are grade 1 and spherical in shape and fine in size and diffusely distributed.
图6b中为经过不含任何变温阶段的真空脉冲渗碳方法处理的齿轮的细小碳化物组织形貌图,碳化物级别为3级(粒块系)。Figure 6b shows the fine carbide structure morphology of the gear treated by the vacuum pulse carburizing method without any temperature change stage, and the carbide grade is grade 3 (grain block system).
图7经过本实施例的变温真空渗碳方法处理的齿轮的渗碳层的硬度-深度分布曲线图,其中渗碳层深度为2.16mm,表面硬度>820HV。Fig. 7 is a hardness-depth distribution curve of the carburized layer of the gear treated by the variable temperature vacuum carburizing method of this embodiment, wherein the carburized layer depth is 2.16mm, and the surface hardness is >820HV.
图8为经过本实施例的变温真空渗碳方法处理的齿轮的接触疲劳强度的检测结果,接触疲劳极限为1921Mpa,比常规渗碳淬火齿轮的接触疲劳极限1638Mpa,提高比例为17.3%。Fig. 8 is the detection result of the contact fatigue strength of the gear treated by the variable temperature vacuum carburizing method of this embodiment, the contact fatigue limit is 1921Mpa, which is 17.3% higher than the contact fatigue limit of the conventional carburizing and quenching gear which is 1638Mpa.
对于本领域技术人员而言,显然本发明不限于上述示范性实施例的细节,而且在不背离本发明的精神或基本特征的情况下,能够以其他的具体形式实现本发明。例如,可以根据工件材质、尺寸等因素确定加热过程是否分段,如分段,则确定各段的加热温度、加热时间、保温时间等。类似地,可以根据工件表层的碳浓度梯度和有效硬化层深度等因素确定脉冲阶的渗碳温度、渗碳阶段的渗碳周期和扩散周期的交替次数、各个周期的持续时间、渗碳周期中的脉冲次数;确定变温阶段中的气体压力、变温温度、变温持续时间、淬火温度、淬火持续时间;以及确定淬火阶段中的具体淬火手段,例如油淬中的油温度,气油复合淬火中的充气压力、充气时间、油温。因此,无论从哪一点来看,均应将实施例看作是示范性的,而且是非限制性的,本发明的范围由所附权利要求而不是上述说明限定,因此旨在将落在权利要求的等同要件的含义和范围内的所有变化囊括在本发明内。It will be apparent to those skilled in the art that the invention is not limited to the details of the above-described exemplary embodiments, but that the invention can be embodied in other specific forms without departing from the spirit or essential characteristics of the invention. For example, it can be determined whether the heating process is segmented according to the workpiece material, size and other factors. If segmented, the heating temperature, heating time, and holding time of each segment are determined. Similarly, the carburizing temperature of the pulse step, the number of carburizing cycles and diffusion cycles in the carburizing stage, the duration of each cycle, and the carburizing cycle can be determined according to the carbon concentration gradient of the workpiece surface and the effective hardened layer depth. The number of pulses; determine the gas pressure, temperature change temperature, temperature change duration, quenching temperature, and quenching duration in the variable temperature stage; and determine the specific quenching means in the quenching stage, such as oil temperature in oil quenching, gas-oil composite quenching in Inflation pressure, inflation time, oil temperature. Accordingly, the embodiments should be regarded in all points of view as exemplary and not restrictive, the scope of the invention being defined by the appended claims rather than the foregoing description, and it is therefore intended that the scope of the invention be defined by the appended claims rather than by the foregoing description. All changes within the meaning and range of equivalents of the elements are embraced in the present invention.
此外,应当理解,虽然本说明书按照实施方式加以描述,但并非每个实施方式仅包含一个独立的技术方案,说明书的这种叙述方式仅仅是为清楚起见,本领域技术人员应当将说明书作为一个整体,各实施例中的技术方案也可以经适当组合,形成本领域技术 人员可以理解的其他实施方式。In addition, it should be understood that although this specification is described according to implementation modes, not each implementation mode only contains an independent technical solution, and this description in the specification is only for clarity, and those skilled in the art should take the specification as a whole , the technical solutions in the various embodiments can also be properly combined to form other implementations that can be understood by those skilled in the art.
以上所述,仅为本发明较佳的具体实施方式,但本发明的保护范围并不局限于此,任何熟悉本技术领域的技术人员在本发明披露的技术范围内,可轻易想到的变化或替换,都应涵盖在本发明的保护范围之内。因此,本发明的保护范围应该以权利要求书的保护范围为准。本文背景技术部分公开的信息仅仅旨在加深对本发明的总体背景技术的理解,而不应当被视为承认或以任何形式暗示该信息构成已为本领域技术人员所公知的现有技术。The above is only a preferred embodiment of the present invention, but the scope of protection of the present invention is not limited thereto. Any person familiar with the technical field can easily conceive of changes or changes within the technical scope disclosed in the present invention. Replacement should be covered within the protection scope of the present invention. Therefore, the protection scope of the present invention should be determined by the protection scope of the claims. The information disclosed in this Background section is only intended to enhance the understanding of the general background of the present invention, and should not be considered as an acknowledgment or any form of suggestion that the information constitutes the prior art that is already known to those skilled in the art.

Claims (8)

  1. 一种获得弥散分布的细小碳化物的变温真空渗碳方法,其特征在于,包括加热阶段、脉冲渗碳阶段、变温阶段、淬火阶段;A variable temperature vacuum carburizing method for obtaining dispersed fine carbides, characterized in that it includes a heating stage, a pulse carburizing stage, a variable temperature stage, and a quenching stage;
    所述脉冲渗碳阶段包括在渗碳温度下交替进行多次渗碳周期和扩散周期,其中在所述渗碳周期中渗碳气体以脉冲方式充入渗碳室,工件表层的碳浓度梯度和有效硬化层深度能够通过所述渗碳周期和所述扩散周期交替进行的次数及每次的持续时间进行调整,所述工件表层的含碳量接近所述渗碳温度下碳在奥氏体中的最大溶解度;The pulse carburizing stage includes alternately performing multiple carburizing cycles and diffusion cycles at the carburizing temperature, wherein in the carburizing cycle, the carburizing gas is pulsed into the carburizing chamber, and the carbon concentration gradient of the surface layer of the workpiece and The effective hardened layer depth can be adjusted by the number of alternate carburizing cycles and the diffusion cycle and the duration of each time. The carbon content of the surface layer of the workpiece is close to the carbon in the austenite at the carburizing temperature. the maximum solubility;
    所述变温阶段包括:在所述脉冲渗碳阶段后向所述渗碳室充入冷却气体以使所述工件表层快速冷却至700℃以下一温度并稳定一段时间,从而使碳化物均匀析出并球化,随后抽至真空,立即升温至淬火温度750℃至980℃并保温一段时间,从而使工件均热且完全奥氏体化;The temperature changing stage includes: filling the carburizing chamber with cooling gas after the pulse carburizing stage to rapidly cool the surface layer of the workpiece to a temperature below 700°C and stabilize it for a period of time, so that carbides are uniformly precipitated and Spheroidizing, then evacuate to vacuum, immediately raise the temperature to the quenching temperature of 750°C to 980°C and hold it for a period of time, so that the workpiece is evenly heated and completely austenitized;
    所述淬火阶段选择以下任一种淬火方式:直接高压气淬、直接油淬、气油复合淬火。In the quenching stage, any one of the following quenching methods is selected: direct high-pressure gas quenching, direct oil quenching, and gas-oil composite quenching.
  2. 根据权利要求1所述的获得弥散分布的细小碳化物的变温真空渗碳方法,其特征在于,在所述变温阶段前还包括至少一个中间变温阶段和至少一个第二脉冲渗碳阶段;The variable temperature vacuum carburizing method for obtaining dispersed fine carbides according to claim 1, further comprising at least one intermediate temperature variable stage and at least one second pulse carburizing stage before the variable temperature stage;
    所述中间变温阶段包括向所述渗碳室充入冷却气体以使工件表层快速冷却至700℃以下一温度并稳定一段时间,从而使碳化物均匀析出并球化,随后抽至真空,立即升温至所述第二脉冲渗碳阶段所需的温度。The intermediate temperature change stage includes filling the carburizing chamber with cooling gas to quickly cool the surface of the workpiece to a temperature below 700°C and stabilize it for a period of time, so that the carbides are uniformly precipitated and spheroidized, and then pumped to a vacuum to raise the temperature immediately to the temperature required for the second pulse carburizing stage.
  3. 根据权利要求2所述的获得弥散分布的细小碳化物的变温真空渗碳方法,其特征在于,The variable temperature vacuum carburizing method for obtaining dispersed fine carbides according to claim 2, characterized in that,
    所述第二脉冲渗碳阶段中的各个渗碳周期和扩散周期的交替次数和持续时间和所述脉冲渗碳阶段的各个渗碳周期和扩散周期的交替次数和持续时间至少部分不同。The number of alternations and durations of the respective carburization cycles and diffusion cycles in the second pulse carburizing stage are at least partially different from the number of alternations and durations of the respective carburizing cycles and diffusion cycles of the pulse carburizing stage.
  4. 根据权利要求1至3任一项所述的获得弥散分布的细小碳化物的变温真空渗碳方法,其特征在于,在所述脉冲渗碳阶段中,所述渗碳温度为750至980℃,渗碳压力为800至1500Pa,所述渗碳周期的总时间和所述扩散周期的总时间的比率为1:2至1:7。The temperature-variable vacuum carburizing method for obtaining dispersed fine carbides according to any one of claims 1 to 3, characterized in that, in the pulse carburizing stage, the carburizing temperature is 750 to 980°C, The carburizing pressure is 800 to 1500 Pa, and the ratio of the total time of the carburizing cycle to the total time of the diffusion cycle is 1:2 to 1:7.
  5. 根据权利要求1至3任一项所述的获得弥散分布的细小碳化物的变温真空渗碳方法,其特征在于,在所述变温阶段中,所述冷却气体的压力≥2×10 5Pa,降温至温度700℃以下后的保温时长为5至60分钟,升温至淬火温度750℃至980℃后的保温时长为5至120分钟。 The variable temperature vacuum carburizing method for obtaining fine carbides dispersedly distributed according to any one of claims 1 to 3, characterized in that, in the variable temperature stage, the pressure of the cooling gas is ≥2×10 5 Pa, The heat preservation time after cooling down to a temperature below 700°C is 5 to 60 minutes, and the heat preservation time after the temperature is raised to a quenching temperature of 750°C to 980°C is 5 to 120 minutes.
  6. 根据权利要求1至5任一项所述的获得弥散分布的细小碳化物的变温真空渗碳方 法,其特征在于,所述渗碳气体为乙炔或丙烷,所述冷却气体为氮气、氩气或氦气。The temperature-variable vacuum carburizing method for obtaining fine carbides dispersedly distributed according to any one of claims 1 to 5, wherein the carburizing gas is acetylene or propane, and the cooling gas is nitrogen, argon or helium.
  7. 根据权利要求1至5任一项所述的获得弥散分布的细小碳化物的变温真空渗碳方法,其特征在于,所述脉冲渗碳阶段的持续时间≥30分钟。The temperature-variable vacuum carburizing method for obtaining dispersed fine carbides according to any one of claims 1 to 5, characterized in that the duration of the pulse carburizing stage is ≥ 30 minutes.
  8. 根据权利要求7所述的获得弥散分布的细小碳化物的变温真空渗碳方法,其特征在于,所述脉冲渗碳阶段的持续时间≥120分钟。The variable temperature vacuum carburizing method for obtaining fine carbides dispersedly distributed according to claim 7, characterized in that the duration of the pulse carburizing stage is ≥ 120 minutes.
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CN113737126B (en) * 2021-09-09 2023-09-29 中国机械总院集团北京机电研究所有限公司 Vacuum carburization method for obtaining dispersed fine carbide
CN115109899A (en) * 2022-06-27 2022-09-27 北京机电研究所有限公司 Heat treatment process of low-carbon alloy steel material
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Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000303160A (en) * 1999-04-19 2000-10-31 Nippon Techno:Kk Carburizing treating method
JP2002212642A (en) * 2001-01-10 2002-07-31 Ntn Corp Gas carburized hardening method of rolling-formed parts and rolling-formed parts obtained with this method
CN1898405A (en) * 2003-12-22 2007-01-17 卡特彼勒公司 Carbide method and article for hard finishing resulting in improved wear resistance
CN101029398A (en) * 2007-03-21 2007-09-05 中国重汽集团济南技术中心有限公司 Gear carburizing quenching process for heavy-duty automobile
JP2016017212A (en) * 2014-07-09 2016-02-01 トヨタ自動車株式会社 Carburizing and quenching method for steel
JP2016033243A (en) * 2014-07-31 2016-03-10 トヨタ自動車株式会社 Carburization treatment method and carburization treatment device of steel material
CN109609893A (en) * 2019-01-22 2019-04-12 北京机电研究所有限公司 A kind of method of thinning microstructure after vacuum carburization
CN110951962A (en) * 2019-12-16 2020-04-03 武汉理工大学 High-performance gear heat treatment method for realizing fine and homogenized structure
CN113737126A (en) * 2021-09-09 2021-12-03 北京机电研究所有限公司 Vacuum carburization method for obtaining dispersed fine carbides

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000303160A (en) * 1999-04-19 2000-10-31 Nippon Techno:Kk Carburizing treating method
JP2002212642A (en) * 2001-01-10 2002-07-31 Ntn Corp Gas carburized hardening method of rolling-formed parts and rolling-formed parts obtained with this method
CN1898405A (en) * 2003-12-22 2007-01-17 卡特彼勒公司 Carbide method and article for hard finishing resulting in improved wear resistance
CN101029398A (en) * 2007-03-21 2007-09-05 中国重汽集团济南技术中心有限公司 Gear carburizing quenching process for heavy-duty automobile
JP2016017212A (en) * 2014-07-09 2016-02-01 トヨタ自動車株式会社 Carburizing and quenching method for steel
JP2016033243A (en) * 2014-07-31 2016-03-10 トヨタ自動車株式会社 Carburization treatment method and carburization treatment device of steel material
CN109609893A (en) * 2019-01-22 2019-04-12 北京机电研究所有限公司 A kind of method of thinning microstructure after vacuum carburization
CN110951962A (en) * 2019-12-16 2020-04-03 武汉理工大学 High-performance gear heat treatment method for realizing fine and homogenized structure
CN113737126A (en) * 2021-09-09 2021-12-03 北京机电研究所有限公司 Vacuum carburization method for obtaining dispersed fine carbides

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