US2157594A - Method of chromizing - Google Patents

Method of chromizing Download PDF

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Publication number
US2157594A
US2157594A US120538A US12053837A US2157594A US 2157594 A US2157594 A US 2157594A US 120538 A US120538 A US 120538A US 12053837 A US12053837 A US 12053837A US 2157594 A US2157594 A US 2157594A
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Prior art keywords
chromium
chromizing
chromized
degrees
alloy
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US120538A
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Hugh S Cooper
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COOPER PRODUCTS Inc
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COOPER PRODUCTS Inc
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Priority to US120538A priority Critical patent/US2157594A/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
    • C23C10/00Solid state diffusion of only metal elements or silicon into metallic material surfaces
    • C23C10/28Solid state diffusion of only metal elements or silicon into metallic material surfaces using solids, e.g. powders, pastes
    • C23C10/34Embedding in a powder mixture, i.e. pack cementation
    • C23C10/36Embedding in a powder mixture, i.e. pack cementation only one element being diffused
    • C23C10/38Chromising
    • C23C10/40Chromising of ferrous surfaces
    • C23C10/42Chromising of ferrous surfaces in the presence of volatile transport additives, e.g. halogenated substances

Definitions

  • This invention relates to the formation of surfacealloys of chrominum on metal objects, and more especially to the formation of such surface alloys on iron and steel.
  • chromizing As applied to chromiumit is known as chromizing.
  • chromizing In the prior art of chromizing it has been customary to use more or less pure chromium powder, with or without certain diluting materials, and often with certain additional or auxiliary compounds such as chlorides or fluorides which seem to aid the process.
  • the present invention relates particularly to such auxiliary material, and to a method of chromizing that utilizes it.
  • An object of this invention is the provision of a novel and improved chromizing material that prevents oxidation of the chromium used.
  • Another object of this invention is the prov vision of a novel and improved chromizing material that prevents oxidation of the substance being chromized.
  • Another object of this invention is the provision of a novel and improved chromizing material that will not attack or react with the articles being chromized.
  • Still another object of this invention is the provision of a novel and improved chromizing material that will prevent the chromizing charge from sintering together.
  • a further object. of the invention is the provision of a novel and improved method of chromizing that produces quickly a deep coating of chromium alloy.
  • the articles to be chromized are packed in a powdered material containing free chromium or a high chromium alloy and then heated at a temperature usually exceeding 1000 degrees C.
  • the heating may be done in a neutral or reducing atmosphere, as hydrogen for instance, and the formation of the surface alloy of chromium may be 60 facilitated by the addition of certain auxiliary compounds to the chromium powder.
  • Various compounds having various degrees of effectiveness have been proposed. for this purpose, and in the main they consist of certain of the metallic l6 halides.
  • Various theories have been proposed to explain the action of some of these compounds. One is that they vaporize below the temperature at which iron oxidizes and thereby displace the oxidizing atmosphere and prevent its action.
  • Another is that they react with the chromium, or a with the iron being chromized, and thereby act as cleaning agents, or as gaseous carriers of chromium, or both.
  • ferrous chloride is an excellent addition agent to a chromizing charge 10 comprising powdered chromium metal, and that it is more effective in promotiong chromizing than any of the materials heretofore proposed, and yet its action cannot be explained by any of the theories so far advanced. Its action is 15 particularly effective at the higher range of chromizing temperatures, that is, from 1100 degrees C. to 1350 degrees C., which are necessary to produce thick layers of surface alloy, that is, say, .050" or more thick. 30
  • This container is then placed in any suitable type of furnace, and in order to help prevent oxidation the entire container, or at least the openings in it, may be covered with a suitable powdered refractory material such as alumina, magnesia, gannister, or
  • the furnace is then brought to temperature, and the heating is carried on at a temperature and for a time governed by the depth of surface alloy desired.
  • the process is operable to a degree on any 45 type of ferrous material such as cast iron, cast steel, simple steel, and alloy steel. In general, however, it works best on low carbon steels, having a carbon content of .25%' or less. Higher carbon content progressively decreases the depth of penetration of the chromium, but the presence of the usual alloying elements other than carbon is not harmful.
  • the composition of the ferrochrome casing produced is not uniform, and the alloy is richest in chromium at the extreme outer surface, the chromium content at that point being about 50%. Toward the interior the chromium content tapers oil progressively to-substantially zero.
  • a chromized article be boiled in nitric acid (about 50% water), that part of the ferro-chrome casing which contains about 12% or more of chromium remains unattacked, while the foundation metal and the remainder of the casing is dissolved away.
  • the thickness of the unattacked casing may be easily measured and is a good criterion of the total thickness 01 casing originally produced. Where thickness of coating or depth of penetration has been mentioned in this specification, it means the thickness or depth of the portion unattacked by nitric acid when treated as above.
  • An article treated according to the present process for about four hours at 1150 degrees C. to 1200 degrees C.
  • Articles chromized in the mixture or charge of this invention come out with a clean bright surface requiring no further treatment.
  • the chromium powder remains unoxidized and retains a clean gray appearance, whereas, ordinarily it turns green by partial oxidation.
  • the chromium does not sinter and may readily be separated from the chromized material, and easily proposed cause sintering at the higher temperatures. and permit a considerable degree of. oxidation and pitting.
  • the use of ferrous chloride therefore produces a novel, desirable, unobvious and unpredictable result.
  • the process of chromizing ferrous metals which comprises embedding the article to be chromized in a powdered charge containing ferrous chloride and a source of chromium metal and subsequently heating the same at a temperature of approximately 1150 degrees C. to 1350 degrees C.

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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)
  • Powder Metallurgy (AREA)

Description

METHOD OF CHROMIZIN G vHugh 8. Cooper, Cleveland Heights, Ohio, as-
signor to Cooper Products, Inc., Cleveland, Ohio, a corporation oi Ohio No Drawing. Application January 14, 1937, Serial No. 120,538
3 Claims.
This invention relates to the formation of surfacealloys of chrominum on metal objects, and more especially to the formation of such surface alloys on iron and steel. When certain metals,
I especially iron and steel, are heated in contact with chromium metal powder under suitable conditions, the chromium penetrates the iron or steel and forms a surface alloy of ferro-chrome. This general process of causing one metal to penetrate another is known as cementation, and
' as applied to chromiumit is known as chromizing. In the prior art of chromizing it has been customary to use more or less pure chromium powder, with or without certain diluting materials, and often with certain additional or auxiliary compounds such as chlorides or fluorides which seem to aid the process.
The present invention relates particularly to such auxiliary material, and to a method of chromizing that utilizes it.
An object of this invention is the provision of a novel and improved chromizing material that prevents oxidation of the chromium used.
Another object of this invention is the prov vision of a novel and improved chromizing material that prevents oxidation of the substance being chromized.
Another object of this invention is the provision of a novel and improved chromizing material that will not attack or react with the articles being chromized.
Still another object of this invention is the provision of a novel and improved chromizing material that will prevent the chromizing charge from sintering together.
A further object. of the invention is the provision of a novel and improved method of chromizing that produces quickly a deep coating of chromium alloy.
Other objects will be apparent from the following description.
In the art of chromizing as commonly practiced the articles to be chromized are packed in a powdered material containing free chromium or a high chromium alloy and then heated at a temperature usually exceeding 1000 degrees C. The heating may be done in a neutral or reducing atmosphere, as hydrogen for instance, and the formation of the surface alloy of chromium may be 60 facilitated by the addition of certain auxiliary compounds to the chromium powder. Various compounds having various degrees of effectiveness have been proposed. for this purpose, and in the main they consist of certain of the metallic l6 halides. Various theories have been proposed to explain the action of some of these compounds. One is that they vaporize below the temperature at which iron oxidizes and thereby displace the oxidizing atmosphere and prevent its action. Another is that they react with the chromium, or a with the iron being chromized, and thereby act as cleaning agents, or as gaseous carriers of chromium, or both.
I have found that ferrous chloride is an excellent addition agent to a chromizing charge 10 comprising powdered chromium metal, and that it is more effective in promotiong chromizing than any of the materials heretofore proposed, and yet its action cannot be explained by any of the theories so far advanced. Its action is 15 particularly effective at the higher range of chromizing temperatures, that is, from 1100 degrees C. to 1350 degrees C., which are necessary to produce thick layers of surface alloy, that is, say, .050" or more thick. 30
In the preferred manner of practicing this invention I use finely powdered chromium metal, or ferro-chrome containing a minor percentage of iron. To this is added finely powdered ferrous chloride. The exact percentage of ferrous chlo- $5 ride is not critical but preferably from 5% to 10% by weight is used. Preferably these two materials are ball-milled together for several hours to mix them thoroughly. To this mixture aluminum oxide, or magnesium oxide, or similar materials, may be added as diluents, but I prefer not to use such additions. The article to be cromized is placed in a suitable metal or ceramic container in which it is completely embedded in this chromizing mixture. This container is then placed in any suitable type of furnace, and in order to help prevent oxidation the entire container, or at least the openings in it, may be covered with a suitable powdered refractory material such as alumina, magnesia, gannister, or
the like. The furnace is then brought to temperature, and the heating is carried on at a temperature and for a time governed by the depth of surface alloy desired.
The process is operable to a degree on any 45 type of ferrous material such as cast iron, cast steel, simple steel, and alloy steel. In general, however, it works best on low carbon steels, having a carbon content of .25%' or less. Higher carbon content progressively decreases the depth of penetration of the chromium, but the presence of the usual alloying elements other than carbon is not harmful. The composition of the ferrochrome casing produced is not uniform, and the alloy is richest in chromium at the extreme outer surface, the chromium content at that point being about 50%. Toward the interior the chromium content tapers oil progressively to-substantially zero. If a chromized article be boiled in nitric acid (about 50% water), that part of the ferro-chrome casing which contains about 12% or more of chromium remains unattacked, while the foundation metal and the remainder of the casing is dissolved away. The thickness of the unattacked casing may be easily measured and is a good criterion of the total thickness 01 casing originally produced. Where thickness of coating or depth of penetration has been mentioned in this specification, it means the thickness or depth of the portion unattacked by nitric acid when treated as above. An article treated according to the present process for about four hours at 1150 degrees C. to 1200 degrees C. will in general have produced thereon an alloy casing about .010" thick, heating for about twenty-four hours at about 1300 degrees C. will produce an alloy casing about .060" thick or thicker. By experience, intermediate temperatures and dura-' tions can be chosen to produce any desired intermediate thickness of casing or depth of penetration.
Articles chromized in the mixture or charge of this invention, and especially those chromized at the higher temperatures necessary to produce so deep penetration, come out with a clean bright surface requiring no further treatment. The chromium powder remains unoxidized and retains a clean gray appearance, whereas, ordinarily it turns green by partial oxidation. Also, the chromium does not sinter and may readily be separated from the chromized material, and easily proposed cause sintering at the higher temperatures. and permit a considerable degree of. oxidation and pitting. The use of ferrous chloride therefore produces a novel, desirable, unobvious and unpredictable result.
Having thus described my invention, I claim:
1. The process of chromizing ferrous metals which comprises embedding the article to be chromized in a powdered charge containing ferrous chloride and a source of chromium metal and subsequently heating the same at a temperature of approximately 1150 degrees C. to 1350 degrees C.
2. The process of chromizing which comprises mbedding the article to be chromized in a pow- Q dered charge containing chromium powder and ferrous chloride and subsequently heating the same for aconsiderable period of time at a temperature above approximately 1150 degrees C.
3. The process of chromizing which comprises embedding the article to be chromized in a powdered charge containing chromium powder and ferrous chloride in a closed vessel and subsequently heating the same for a considerable period of time at a temperature above approximately 1150 degrees C. I
HUGH S. COOPER crushed for re-use. In contrast ferric chloride and other compounds that have been-
US120538A 1937-01-14 1937-01-14 Method of chromizing Expired - Lifetime US2157594A (en)

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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2415078A (en) * 1940-07-17 1947-02-04 Becker Gottfried Process for chroming steel articles
US2685543A (en) * 1951-01-17 1954-08-03 Wearex Corp Production of chromium carbide surfaced wear resistant ferrous bodies
US2809127A (en) * 1948-11-19 1957-10-08 Metal Gas Company Ltd Surface treatment of metals
US2855332A (en) * 1954-09-07 1958-10-07 Metal Diffusions Inc Method of chromizing ferrous metal
US2899332A (en) * 1959-08-11 Chromizing method and composition
DE974190C (en) * 1949-08-05 1960-10-13 Onera (Off Nat Aerospatiale) Device for the production of metallic diffusion coatings
DE1224583B (en) * 1961-10-18 1966-09-08 Alloy Surfaces Co Inc Chromating agents and process for their preparation
US3449159A (en) * 1966-02-14 1969-06-10 Alloy Surfaces Co Inc Process for forming metal coatings
US4099993A (en) * 1973-01-26 1978-07-11 Hermann Muller Process for producing an extremely hard mixed carbide layer on ferrous materials to increase their resistance to wear
US4249961A (en) * 1976-03-06 1981-02-10 Harri Nevalainen High strength steel for diffusion chromizing

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2899332A (en) * 1959-08-11 Chromizing method and composition
US2415078A (en) * 1940-07-17 1947-02-04 Becker Gottfried Process for chroming steel articles
US2809127A (en) * 1948-11-19 1957-10-08 Metal Gas Company Ltd Surface treatment of metals
DE974190C (en) * 1949-08-05 1960-10-13 Onera (Off Nat Aerospatiale) Device for the production of metallic diffusion coatings
US2685543A (en) * 1951-01-17 1954-08-03 Wearex Corp Production of chromium carbide surfaced wear resistant ferrous bodies
US2855332A (en) * 1954-09-07 1958-10-07 Metal Diffusions Inc Method of chromizing ferrous metal
DE1224583B (en) * 1961-10-18 1966-09-08 Alloy Surfaces Co Inc Chromating agents and process for their preparation
US3449159A (en) * 1966-02-14 1969-06-10 Alloy Surfaces Co Inc Process for forming metal coatings
US4099993A (en) * 1973-01-26 1978-07-11 Hermann Muller Process for producing an extremely hard mixed carbide layer on ferrous materials to increase their resistance to wear
US4249961A (en) * 1976-03-06 1981-02-10 Harri Nevalainen High strength steel for diffusion chromizing

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