US2399848A - Process for the introduction of chromium into steel articles - Google Patents
Process for the introduction of chromium into steel articles Download PDFInfo
- Publication number
- US2399848A US2399848A US339132A US33913240A US2399848A US 2399848 A US2399848 A US 2399848A US 339132 A US339132 A US 339132A US 33913240 A US33913240 A US 33913240A US 2399848 A US2399848 A US 2399848A
- Authority
- US
- United States
- Prior art keywords
- chromium
- carbon
- articles
- introduction
- steel
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C10/00—Solid state diffusion of only metal elements or silicon into metallic material surfaces
- C23C10/28—Solid state diffusion of only metal elements or silicon into metallic material surfaces using solids, e.g. powders, pastes
- C23C10/34—Embedding in a powder mixture, i.e. pack cementation
- C23C10/36—Embedding in a powder mixture, i.e. pack cementation only one element being diffused
- C23C10/38—Chromising
- C23C10/40—Chromising of ferrous surfaces
Definitions
- the surface of iron and steel articles may be enriched in chromium by diffusion.
- Vaporisable chromium compounds have recently been used for the introduction of chromium and especially vaporous chromium chlorine compounds, of which chromium chloride has proved to be peculiarly suitable.
- vaporisable chromium chlorine compounds By using vaporisable chromium chlorine compounds a considerable reduction of the high treating temperatures and of the treating period has been ob.- tained, e. g. the treating temperature has been reduced to 1000 and the treating period to some 5 hours, in the course of which good chromium layers ma be obtained on the surface to depths of 0.1 mm. on an average.
- the procedure of the chromium diffusion and the quality of the chromium layers formed on the surfaces also depend upon the composition of the materials to be treated; it is known that the chromium diffusion is rendered difllcult with increasing carbon content of the same. For this reason, iron alloys having not more than 0.2%, possibly not more than 0.1%, have so far been demanded for the introduction of chromium.
- this can be counteracted by adding to the alloys having such a value of F(b) certain 7 elements, which suppress the migration of the carbon in the cross section, e. g. titanium, manganese, niobium or aluminium.
- the drawing graphically illustrates in detail the reciprocity between the diifusion process and the quality of the chromium layer on the surface 2 assasss diifusion specially good chromiferoug surfaces onnon-alloyed' iron or steel.
- the space between the curve AB and the co-ordinates encloses therefore the conditions which are to be observed in case of non-alloyed kinds of iron and steel in order to obtain chromium zones which can stand a. g. strong deformations like a bending radius of about 2 mm. and which fully resist considerable wet corrosion. .(Test in the salt water spray box.)
- the articles to be treated can be made of non-alloyed sorts of iron and steel and the carbon content of thesamecanbearrangedwithrespecttothewali size of the articles so as to conform with the conditions of the space between the curves AB andCD- Whilst chromiierous surfaces of the good propertiesofthespacebelowthe curve ABcanbe well obtained in the space above the curve CD by completely binding the carbon content of the used alloys y means of titanium, vanadium, niobium or the like, chromium zones of the properties corresponding to those which are met in the space between the curves AB and CD can also be obtained above the curve CD, by adding to the iron carbon, alloys from which the articles are made smaller quantities of titanium, vanadium, niobium or the like than are necessary for :efimpletely binding the carbon content of the To recapitulate, the invention first discloses the knowledge that.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
- Solid-Phase Diffusion Into Metallic Material Surfaces (AREA)
- Physical Vapour Deposition (AREA)
Description
May 7, 1946. G. BECKER ET AL 2,399,348 PROCESS FOR THE INTRODUCTION OF CHROMIUM INTO STEEL ARTICLES Filed June 6, 1940 Patented May 7, 1946 UNITED PROCESS FOR THE INTRODUCTION OF CHROMIUM INTO STEEL ARTICLES Gottfried Becker, Buderich, near Dusseldorf, Karl Daeves, Dusseldorf, and Fritz Steinberg, Dusseldorf-Eller, Germany; vested in the Allen Property Custodian Application June .6, 1940, Serial No. 339,132 In Germany June 8, 1939 1 Claim. (01. 11'7--22l This invention relates to improvements in or relating to a process for the introduction of chromium into iron or steel articles.
As is known, the surface of iron and steel articles may be enriched in chromium by diffusion.
' This was done, according to previousmethods,
b packing the articles in chromium powder or ferrochrome powder and then heating the whole for many hours to very high temperatures, e, g. 1200 to 1300" C. Vaporisable chromium compounds have recently been used for the introduction of chromium and especially vaporous chromium chlorine compounds, of which chromium chloride has proved to be peculiarly suitable. By using vaporisable chromium chlorine compounds a considerable reduction of the high treating temperatures and of the treating period has been ob.- tained, e. g. the treating temperature has been reduced to 1000 and the treating period to some 5 hours, in the course of which good chromium layers ma be obtained on the surface to depths of 0.1 mm. on an average.
The procedure of the chromium diffusion and the quality of the chromium layers formed on the surfaces also depend upon the composition of the materials to be treated; it is known that the chromium diffusion is rendered difllcult with increasing carbon content of the same. For this reason, iron alloys having not more than 0.2%, possibly not more than 0.1%, have so far been demanded for the introduction of chromium.
However, experiments on a large scale have shown that a low-carbon prime material alone does not lead directly to a good progress of the introduction of chromium and to useful surfaces, because, as has been found, such results do not depend upon the proportion of carbon but upon the total amount of the carbon in the material. It has been found that, when introducing the chromium, migration of the carbon from the interior of the cross section towards the surface takes place, and this migration is the stronger, the greater the carbon of the cross section. Thus. for instance, it is not possible, when the diffusion is carried out under the usual conditions, to produce satisiactory layers on an article made from steel of about 0.02% carbon content and having a wall size of about mm., whereas very good and tough chromium zones are obtainable on the same steel and under the same conditions, if the article has a wall size of some 2 mm. This clearly demonstrates that, with respect to the diffusion process and the quality of the chromium layers formed on the surface, the wall size of the articles to be treated and the carbon content of the material to be treated depend upon each other and that there must be certain limits in this function, above which no useful chromium layers and below which very useful ones may be obtained. In view of the fact that it has been ascertained by previous experiments that the disadvantageous influence of the carbon may be suppressed by adding certain alloying elements to the iron, e. g. titanium, vanadium, niobium, manganese or aluminium, it is possible in each casemaking use of the firm relation existing between the wall size and the carbon content of the articles to be treated-42o produce with absolute certainty and in a most economical way useful chromiferous surfaces on iron or steel articles of even higher carbon content and with an ample wall size tolerance.
The firm relation existing between the wall size and the carbon content with respect to the diffusion process and the quality of the chromi um layers formed on the surface is, according to the invention, determined by the equation a.b=F(b), in which equation a is the wall size in millimetres and b the percentage of the carbon content. If F(b) exceeds a certain value in this equation, satisfactory chromium layers 0 n no longer be produced on the surface of articlesfrom pure iron-carbon alloys, 1. e. there will result, when the diffusion is carried on under the usual conditions, chromiferous zones which are brittle and have a relatively low resistance to corrosion. However, according to the present invention, this can be counteracted by adding to the alloys having such a value of F(b) certain 7 elements, which suppress the migration of the carbon in the cross section, e. g. titanium, manganese, niobium or aluminium.
The value of PG?) above which the quality of the chromiferous surfaces is no longer satisfactory without additional alloying steps, and below which there will result in each case very good and useful chromiferous surfaces, may be substituted, in a manner which is absolutel suflicient for practise, for three roughly graduated ranges of carbon content, by certain constants. For the lowest range of carbon up toabout 0.05% C this constant is 0.08, for the range of about 0.1% to about 0.4% C this constant is 0.12,, and for a range of 0.5 to about 1.5% C the constant is 0.17. These constants representing practical approximations only, are subject to a variation of :0.02
max.
The drawing graphically illustrates in detail the reciprocity between the diifusion process and the quality of the chromium layer on the surface 2 assasss diifusion specially good chromiferoug surfaces onnon-alloyed' iron or steel. The space between the curve AB and the co-ordinates encloses therefore the conditions which are to be observed in case of non-alloyed kinds of iron and steel in order to obtain chromium zones which can stand a. g. strong deformations like a bending radius of about 2 mm. and which fully resist considerable wet corrosion. .(Test in the salt water spray box.)
If it is intended to obtain the same properties of the chromiferous surfaces in case of wall sizes and carbon contents above those of the curve AB, it is, according to the invention, no longer possible to use pure iron or steel for the production of the articles to be treated, but it is necessary to use iron-carbon alloys, which contain additions of titanium, vanadium, niobium or of elements of similar effect, and that at least up to such an amount that the total carbon content of the alloy is bound by them. The same effect canalso be obtained by adding manganese or aluminium, e. g. to form an alloy which contains, apart from about 0.1% carbon, about 3% manganese.
The transition of the properties of the chromiferous surfaces from the space below the curve AB to the space above the curve is not sudden, but between the curve AB and a further curve CD having a constant value for 1"(b) which is by 0.06 higher, there is a space in which also nonalloyed kinds of iron and steel may still be coated by chromiierous layers which stand average deformations like light bending etc. and which resist humid air. This resistance is also indicated by non-corrosion in 30 percent hot nitric acid. It, therefore. it is intended to obtain chromiferous surfaces of this average quality only, the articles to be treated can be made of non-alloyed sorts of iron and steel and the carbon content of thesamecanbearrangedwithrespecttothewali size of the articles so as to conform with the conditions of the space between the curves AB andCD- Whilst chromiierous surfaces of the good propertiesofthespacebelowthe curve ABcanbe well obtained in the space above the curve CD by completely binding the carbon content of the used alloys y means of titanium, vanadium, niobium or the like, chromium zones of the properties corresponding to those which are met in the space between the curves AB and CD can also be obtained above the curve CD, by adding to the iron carbon, alloys from which the articles are made smaller quantities of titanium, vanadium, niobium or the like than are necessary for :efimpletely binding the carbon content of the To recapitulate, the invention first discloses the knowledge that. with respect to the diifusion process and the quality of the chromium layers produced on the surfaces, the wall size and the carbon content of the articles to be treated dea diiiusion, i. e. for the diifusion in pure metallic condition as well as for the diffusion by means of vaporisable or vaporous chromium compounds, specially chromium chlorine compounds.
We claim:
as A method of producing ferrous metal articles of dimensions and compositions in which the product of the wall thickness in millimeters and the carbon content in percentage exceeds the value represented by curve AB in the accom- 40 panying drawing, which comprises including in the composition of which the articles are fashioned about 3% of manganese and 0.1% carbon, and diflusing chromium into the surface of the article.
GO'I'I'FRIED BECKER. KARL DAEVES. FRITZ STEINBERG.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2399848X | 1939-06-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
US2399848A true US2399848A (en) | 1946-05-07 |
Family
ID=7995789
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US339132A Expired - Lifetime US2399848A (en) | 1939-06-08 | 1940-06-06 | Process for the introduction of chromium into steel articles |
Country Status (1)
Country | Link |
---|---|
US (1) | US2399848A (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2791517A (en) * | 1953-11-30 | 1957-05-07 | Deutsche Edelstahlwerke Ag | Chromium-coating steel surfaces by the diffusion process |
US2792657A (en) * | 1946-05-16 | 1957-05-21 | Battelle Development Corp | Gun barrel coated with tantalum |
US2875112A (en) * | 1955-06-13 | 1959-02-24 | Deutsche Edelstahlwerke Ag | Process for improving the physical properties of chromized articles |
US3108013A (en) * | 1960-01-28 | 1963-10-22 | Pfaudler Permutit Inc | Method of chromizing |
DE1159238B (en) * | 1954-03-05 | 1963-12-12 | Deutsche Edelstahlwerke Ag | Material for rust-resistant, gas-chromed steel objects |
US3118762A (en) * | 1960-07-25 | 1964-01-21 | Weatherley Eric George | Diffusion process for the manufacture of a malleable iron-chromium alloy |
US3620816A (en) * | 1968-10-16 | 1971-11-16 | John J Rausch | Method of diffusion coating metal substrates using molten lead as transport medium |
US3969550A (en) * | 1973-08-13 | 1976-07-13 | National Steel Corporation | Chromizing process using columbium as stabilizer |
US4042426A (en) * | 1975-03-10 | 1977-08-16 | National Steel Corporation | Chromized steel substrate |
US4526817A (en) * | 1982-11-01 | 1985-07-02 | Material Sciences Corporation | Process for surface diffusing steel products in coil form |
-
1940
- 1940-06-06 US US339132A patent/US2399848A/en not_active Expired - Lifetime
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2792657A (en) * | 1946-05-16 | 1957-05-21 | Battelle Development Corp | Gun barrel coated with tantalum |
US2791517A (en) * | 1953-11-30 | 1957-05-07 | Deutsche Edelstahlwerke Ag | Chromium-coating steel surfaces by the diffusion process |
DE1159238B (en) * | 1954-03-05 | 1963-12-12 | Deutsche Edelstahlwerke Ag | Material for rust-resistant, gas-chromed steel objects |
US2875112A (en) * | 1955-06-13 | 1959-02-24 | Deutsche Edelstahlwerke Ag | Process for improving the physical properties of chromized articles |
US3108013A (en) * | 1960-01-28 | 1963-10-22 | Pfaudler Permutit Inc | Method of chromizing |
US3118762A (en) * | 1960-07-25 | 1964-01-21 | Weatherley Eric George | Diffusion process for the manufacture of a malleable iron-chromium alloy |
US3620816A (en) * | 1968-10-16 | 1971-11-16 | John J Rausch | Method of diffusion coating metal substrates using molten lead as transport medium |
US3969550A (en) * | 1973-08-13 | 1976-07-13 | National Steel Corporation | Chromizing process using columbium as stabilizer |
US4042426A (en) * | 1975-03-10 | 1977-08-16 | National Steel Corporation | Chromized steel substrate |
US4526817A (en) * | 1982-11-01 | 1985-07-02 | Material Sciences Corporation | Process for surface diffusing steel products in coil form |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2399848A (en) | Process for the introduction of chromium into steel articles | |
US2266481A (en) | Age hardenable, low expansion, nickel-iron-titanium alloy | |
US3676109A (en) | Rust and heat resisting ferrous base alloys containing chromium and aluminum | |
JPS6017818B2 (en) | A sintered powder compact useful as a cutting tool and its manufacturing method | |
US2240940A (en) | Aluminum alloy | |
US3146096A (en) | Weldable high strength magnesium base alloy | |
US2255482A (en) | Process which consists in causing chromium to diffuse | |
US2813788A (en) | Nickel-chromium-iron heat resisting alloys | |
US2137144A (en) | Process for the production of metal carbides | |
US1892316A (en) | Noncorrosive steel alloy | |
US2317980A (en) | Magnesium-base alloy | |
US2242865A (en) | Nickel alloy | |
US1941368A (en) | Nickel alloys | |
US1307853A (en) | Assigwob | |
US1919211A (en) | Alloy steel | |
US2097024A (en) | Production of a protective layer on iron | |
US2153906A (en) | Method of heat treating chromiumcontaining corrosion and/or heat resisting steels | |
US2253385A (en) | Steel | |
US1704253A (en) | Plastic light aluminum alloy and process oe producing same | |
US2103610A (en) | Alloy steels | |
US1572744A (en) | Nickel alloy and method of making the same | |
US1932848A (en) | Aluminum alloys | |
US2325044A (en) | Manganese alloys | |
US1365178A (en) | Aluminum alloy and method of making same | |
US1831987A (en) | Magnesium-tin-zinc alloys |