GB2076434A - Heat treatment of metals - Google Patents

Heat treatment of metals Download PDF

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Publication number
GB2076434A
GB2076434A GB8113550A GB8113550A GB2076434A GB 2076434 A GB2076434 A GB 2076434A GB 8113550 A GB8113550 A GB 8113550A GB 8113550 A GB8113550 A GB 8113550A GB 2076434 A GB2076434 A GB 2076434A
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Prior art keywords
furnace
atmosphere
metal
volume
ammonia
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GB8113550A
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GB2076434B (en
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BOC Ltd
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BOC Ltd
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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
    • C23C8/80After-treatment
    • 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
    • C23C8/28Solid 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 more than one element being applied in one step
    • C23C8/30Carbo-nitriding
    • C23C8/32Carbo-nitriding of ferrous surfaces

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Solid-Phase Diffusion Into Metallic Material Surfaces (AREA)

Abstract

Ferrous metal is treated by austenitic nitro-carburising in a heat treatment furnace. A suitable atmosphere is created by admitting to the furnace nitrogen; ammonia; and a liquid or vaporous organic compound of carbon, hydrogen and oxygen. The atmosphere is maintained at a temperature in the range 690 to 750 DEG C. The organic compound is typically methanol and the atmosphere typically comprises nitrogen, carbon monoxide, hydrogen and free ammonia as well as small amounts of methane, carbon dioxide and water vapour. After being removed from the furnace, the ferrous metal is quenched. It has an outer surface layer of white, scuff-resistant, epsilon compound and an inner carbo-nitrided case containing austenitic and martensitic zone. The ferrous metal may then be treated to convert austenite to martensite or lower bainite.

Description

SPECIFICATION Heat tratment of metals This invention relates to the heat treatment of metals.
One method of heat treatment, in daily commercial use, is the carbonitriding of low carbon steels. If the components to be carbonitrided are of relatively thin cross-section they tend to become physically distorted.
Attempts have therefore been made to find alternative heat treatment processes to carbonitriding in order to avoid this problem of distortion. One such process is ferritic nitrocarburising. It has been found that the process of ferritic nitro-carburising of mild steel components enables the problem of distortion to be overcome and enables a scuff-resistant surface finish to be obtained. One drawback of the process of ferritic nitro-carburising is, however, that the components, after treatment by the process, tend to have poor indentation resistance. Another process which overcomes the aforementioned problem of distortion is austenitic nitrocarburising. Moreover, mild steel components can be given good scuff-resistance and indentationresistance by being subjected to austenitic nitrocarburising.
In order to perform a process of austenitic nitrocarburising of components of mild or other low carbon steel, it has hitherto been the practice to produce the necessary atmosphere by adding ammonia to an atmosphere produced by an endothermic generator and to supply the resultant gas mixture (or the two gas streams separately) to a furnace (typically a sealed quench furnace) in which the treatment is performed. Endothermic generators do however have certain disadvantages. In particular, they can be expensive to maintain, and skilled operatives are often required for this purpose; they are relatively expensive items of capital equipment which have a finite life; and they are quite bulky and take up floorspace which could otherwise be used for a different purpose in a heat treatment workshop.
We have now found that it is possible to provide a suitable atmosphere for austenitic nitrocarburising of steel or other ferrous metal without using an endothermic generator.
According to the present invention there is provided a method of austenitic nitro-carburising ferrous metal in a heat treatment furnace, in which method a suitable atmosphere is created by admitting to the furnace nitrogen; ammonia; and a liquid or vaporous organic compound of carbon, hydrogen and oxygen and is maintained at a temperature in the range 690 to 7500C.
The said compound is preferably methanol.
Preferably for each unit volume of ammonia admitted to the furnace, two unit volumes of nitrogen are supplied thereto, and for each (standard) cubic foot of nitrogen, one-sixtieth of a litre of methanol (measured as a liquid) is supplied to the furnace. In other words, preferably for each 2 moSes of nitrogen admitted to the furnace, 2 moles of methanol and 1 mole of ammonia are admitted to the furnace. The methanol may be dripped into the furnace, or maybe vaporised upstream of the furnace and introduced as a vapour into the furnace.
Typically, the nitrogen for use in the process is stored in liquid state in an insulated vessel and vaporised upsteam of the furnace.
In the furnace the methanol decomposes and a gas mixture comprising nitrogen, hydrogen, carbon monoxide, carbon dioxide, water vapour and methane is formed. Furthermore, most but not all of the ammonia decomposes to form nitrogen and hydrogen. Thus, the furnace atmosphere comprises nitrogen, hydrogen, carbon monoxide, water vapour, methane and ammonia. Preferably, the atmosphere includes 7 to 1 1% by volume of carbon monoxide; from 30 to 40% by volume of hydrogen, and from 6 to 11% by volume of free ammonia. With such levels of carbon monoxide, hydrogen and free ammonia, the atmosphere typically includes from 1 to 2% by volume of carbon dioxide and from 2 to 3% by volume of methane and has a dew point between -50C and +50C.Such an atmosphere may be formed in, for example, a sealed quench furnace at 7000C by admitting to the furnace 120 cubic feet per hour of nitrogen, 60 cubic feet per hour of ammonia and 2 litres per hour of methanol (measured as liquid). In one example, we have found that a furnace atmosphere, comprising 36% by volume of hydrogen; 9% by volume of carbon monoxide; 8.5% by volume of ammonia; 2.6% by volume of methane; 1.3% by volume of carbon dioxide and balance nitrogen, with a dew point in the range -20C to +20C, is produced. If desired the proportion of free ammonia in the furnace may be controlled by using a dissociation burette.
Typically, the components to be nitrocarburised may be kept in the atmosphere at a temperature of 690 C to 7500C for a period of 2 hours. During this period a relatively thin, white, outer layer is formed at the surfaces of the components (or other work) to be treated. This layer is of the kind referred to in the art as being of epsilon compound, and includes oxygen, nitrogen and carbon. The outer layer has scuff-resistant properties. In addition to the outer layer there is an inner carbo-nitrided case surrounding a ferritic core. After quencing the components in oil, the case has two zones, one austenitic and the other martensitic. It is then desirable to transform the austenite to lower bainite or martensite so as to optimise the mechanical properties of the case.
The transformation to lower bainite is typically effected isothermally by tempering at 2500C or above for at least one hour (and preferably at 3000C or above for at least two hours). The transformation to martensite is effected by reducing the temperature of the components to -700C or below, and then allowing the components to return to ambient temperature. In order to prevent the austenite from stabilising it is desirable to start to reduce the temperature of the components to -700C oi below within two hours of completion of the (oil) quench.
Typically, if the components are of mild steel and if they are maintained in the furnace atmosphere at 7OO0C for two hours, the (outer) layer of epsilon compound has a depth of from 0.0010 to 0.0012 inches and the (inner) case has a depth of from 0.005 to 0.006 inches.
Typical micro-hardness traverses on samples of mild steel that has been subjected to austenitic nitro-carburising in accordance with the invention are shown in the accompanying drawing which is a graph showing how the hardness (HV x 0.1) of the samples vary with increasing depth of sample.
The results for three samples are shown in the graph. All samples were maintained for two hours in an atmosphere, at 700 C, of the kind described herein. The austenite of a first sample was transformed isothermally to lower bainite by tempering for two hours at 30006, and the austenite of a second sample was transformed to martensite by reducing the temperature of the sample to 700 C, while the third sample was given no treatment to transform its austenite. The first sample has a surface more ductile but less hard than that of the second surface.
The invention also includes within its scope ferrous metal that has been treated by a method of austenitic nitro-carburising as described herein.

Claims (14)

1. A method of austenitic nitro-carburising ferrous metal in a heat treatment furnace, in which method a suitable atmosphere is created by admitting to the furnace nitrogen; ammonia; and a liquid or vaporous organic compound of carbon, hydrogen and oxygen and is maintained at a temperature in the range 690 to 75O0C.
2. A method is claimed in claim 1, in which the said compound is methanol.
3. A method is claimed in claim 2, in which for each 2 moles of nitrogen admitted to the furnace, 2 moles of methanol and 1 mole of ammonia are admitted to the furnace.
4. A method as claimed in any one of the preceding claims, in which an atmosphere is created in the furnace inciuding 7 to 1 1% by volume of carbon monoxide; 30 to 40% by volume of hydrogen, and from 6 to 1 1% by volume of free ammonia.
5. A method as claimed in claim 4, in which the atmosphere additionally includes carbon dioxide, methane and water vapour.
6. A method as claimed in claim 5, in which the atmosphere includes from 1 to 2% by volume of carbon dioxide, and from 2 to 3% by volume of methane, and has a dew point in the range to +50C.
7. A method as claimed in any one of the preceding claims, in which the ferrous metal is maintained in the atmosphere for at least two hours.
8. A method as claimed in claim 7, in which the metal is then quenched.
9. A method as claimed in claim 8, in which after quencing austenite in the metal is transformed isothermally to lower bainite.
10. A method as claimed in claim 9, in which the transformation is effected by tempering the metal at a temperature of at least 250 C for at least one hour.
11. A method as claimed in claim 10, in which the metal is tempered at a temperature of at least 300"C for at least 2 hours.
12. A method as claimed in claim 8, in which, after quencing, austenite in the metal is transformed to martensite.
13. A method as claimed in claim 12, in which the transformation is effected by reducing the temperature of the metal to -700C or below.
14. Articles of ferrous metal that has been treated by a method as claimed in any one of the preceding claims.
GB8113550A 1980-05-02 1981-05-01 Heat treatment of metals Expired GB2076434B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB8113550A GB2076434B (en) 1980-05-02 1981-05-01 Heat treatment of metals

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Application Number Priority Date Filing Date Title
GB8014576 1980-05-02
GB8113550A GB2076434B (en) 1980-05-02 1981-05-01 Heat treatment of metals

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GB2076434A true GB2076434A (en) 1981-12-02
GB2076434B GB2076434B (en) 1984-06-27

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115572937A (en) * 2022-10-28 2023-01-06 西安理工大学 High-hardness antifriction steel wire ring and preparation method thereof
CN115612972A (en) * 2022-09-27 2023-01-17 南京丰东热处理工程有限公司 Steel surface layer thickness controllable nitrogen-containing martensite composite modified layer and process method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115612972A (en) * 2022-09-27 2023-01-17 南京丰东热处理工程有限公司 Steel surface layer thickness controllable nitrogen-containing martensite composite modified layer and process method thereof
CN115572937A (en) * 2022-10-28 2023-01-06 西安理工大学 High-hardness antifriction steel wire ring and preparation method thereof

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Publication number Publication date
GB2076434B (en) 1984-06-27

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PE20 Patent expired after termination of 20 years

Effective date: 20010430