US2101950A - Preparing metal for enameling - Google Patents

Preparing metal for enameling Download PDF

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US2101950A
US2101950A US716674A US71667434A US2101950A US 2101950 A US2101950 A US 2101950A US 716674 A US716674 A US 716674A US 71667434 A US71667434 A US 71667434A US 2101950 A US2101950 A US 2101950A
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nickel
iron
metal
coating
sheet
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US716674A
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George W Mcgohan
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American Rolling Mill Co
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American Rolling Mill Co
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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
    • C23C18/00Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
    • C23C18/02Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition
    • 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
    • C23DENAMELLING OF, OR APPLYING A VITREOUS LAYER TO, METALS
    • C23D3/00Chemical treatment of the metal surfaces prior to coating

Definitions

  • My invention relates to providing an initial coating of metallic substance, comprising an adhesion promoting-metal, preferably nickel, on
  • my invention provides a 10 method of forming in the surface elements of a sheet or other piece of metal an extremely small thickness of coating which greatly assists in promoting adhesion of a subsequently applied coating of vitreous enamel.
  • My method has the advantage of being subject to accurate control, and is admirably adapted to use at the rolling mill where the iron or steel sheets are prepared.
  • Sheets which are very low in carbon are recognized as the best for vitreous enameling, and while my method can be applied to steel of higher carbon content, the very low carbon is the best. Also,-although my coating is productive of most excellent bond of a first'coat of enamel even on a cold rolled high finish sheet, still if applied to a sheet which has been sand blasted or is roughened in-some other way, it will be easier to build up a first coat of desired thickness thereon prior to firing (of enamel).
  • My method has the further advantageof' permitting the formation of the desired surface coat- 40 ing at various stages in the process of manufacturing the sheets themselves. Thus it is-possible usual way. I am-able thus to allocate the coat- -ing operation to any convenient point'in the processing sequence, and in particular to arrange to employ such heating stepor steps as form a part.
  • I may take an iron sheet and dip it in a solution of about 3 to 5% nickel sulphate, and then dry the sheet and raise it to a temperature of around 700 Fahr. or greater, with the result 2 of forming on the sheet a very thin coating of nickel, nickel iron alloy or at least of some nickel
  • a sulphuric acid pickling bath of usual iron and steel pickling concentration I find that the nickel iron alloy is unaffected and/or any decomposable nickel compound is reduced, and/on'if reduction has already taken place, other undesirable reaction products are removed, as will hereinafter be 30 explained.
  • I I may apply the-sulphatesolution to a hotrolled sheet prior'to pickling-and only pickle the product once after the annealing.
  • the thin scale does not seem to interfere with the treatment resulting in the formation of metallic nickel alloy on the surface of the sheet. I prefer, however, to pickle and remove the scale by washing the bars or other material from which the sheets are rolled and then proceed to the dipping in nickel sulphate solution prior to final rolling.
  • the heating step is an essential part of the process, for the purp se of decomposing the nickel salt. Not only would a coatin of nickel salt as such, 1. e., without the heating step, be lacking in ultimate adhesion, but it would be highly undesirable in the enameling step because of the setting-up effect of the nickel salt upon the enamel itself.
  • a coatin of nickel salt as such, 1. e., without the heating step, be lacking in ultimate adhesion, but it would be highly undesirable in the enameling step because of the setting-up effect of the nickel salt upon the enamel itself.
  • An ultimate pickling step is of importance, not only to possibly effect the reduction of any nickel compounds which persist but also to remove the iron sulphide produced as I have indicated above.
  • this pickling need not immediately follow the heat treatment, but may be any pickling which is incident to the process of producing sheets at the rolling mill, or may even be, as I have indicated above, the usual pickling applied to the sheets by the enameler.
  • coatings of nickel or the like may be produced on pieces for rolling, such as sheet bars, rough plate or thin bars,-by the steps of coating with the salt of the coating metal, followed by a heat treatment,
  • thin bars produced as usual on the roughing mill, are preferably pickled to obtain. a clean surface which will be easily wet.
  • the pickled thin bars are then wetted with a nickel solution, preferably by running them between rag I rolls soakedwith the solution, whereupon they may or may not be dried. They are then heated for hot reduction of thickness in the usual manner and are processed according to the ordinary veniently be located in the production line. 01-.-
  • pickled thin bars are coated as described, and then are heated in a furnace at approximately 1000 to 1500 Fahr., which forms the nickel alloy on the surface of the bars.
  • the heating of the thin bars is, of course, an extra operation, but is necessary for reasons which will be clear from thelforegoing explanation.
  • the heating at'approximately 1000 to 1500 Fahr. forms a thin gray-blue oxide on the sheets, which is very tightly adhering.
  • the heating forms'the nickel alloy in the surface elements of the sheet or bar so that it is not removed during the cold reduction.
  • the scale which I have Just described, does not appear to have any detrimental effect upon the rolls in the cold mills, and it has the advantage of providing an ultimate pickled sheet the surfaces of which are alloyed with nickel and are also slightly roughened. This likewise promotes adhesion of the enamel.
  • nickel sulphate is approximately 55 to 60 grams of nickel sulphate (NiSO4.6H2O) per cc. of solution, applied to rolling pieces of twice the final thickness.
  • the desirable. thickness of nickel deposit according to my investigation is between '.03 and .10 gram per square foot of surface as determined by chemical analysis. It can be regulated by controlling the concentration of nickel sulphate solution in which the sheet is initially dipped. A suitable dried film of nickel sulphate [weighing from .14 gram per square foot to .46
  • a cobalt flashing can be applied by following my method, also other salts than the sulphate salt of adhesion promoting metals can be used but I preferably employ nickel sulphate because it is quite inexpensive.
  • the product in sheet form may be shipped to the enameler and by him formed into shape, followed by the usual pickling and cleaning methods, without interfering with the effectiveness of the coating.
  • a process of preparing iron or steel for vitreous enameling which consists in coating the metal with a heat decomposable salt of an adherence enhancing metal, heating the metal to decompose the salt and form a thin coating of the adherence enhancing metal alloyed with the iron or steel and'acid treating the product, said metal being nickel.
  • a process for the purposedescribed which comprises coating iron or steel pieces with a sulphate salt of an adhesion promoting metal for enameling work, decomposing said salt on the surface of said pieces by a heat treatment whereby in part at least, an alloy of iron and the adhesion promoting metal is'produced, together
  • sheet with a compound or iron and sulphur and alterward pickling said pieces sufllciently at ieast to decompose said compound of iron and sulphur.
  • a process of preparing iron or steel for vitreous enameling which comprises dipping iron or steel pieces in awate'r solution of a. heat decomposable'salt of an adherence enhancing metal chosen from a group consisting of cobalt and nickel, and drying and heating the metal to decompose the salt and form a thin coating of the adherence enhancing metal alloyedwith the iron or steel, afterward acid treating said pieces.
  • a process 'of preparing iron or steel for vitreous enameling which comprises coating iron or steel pieces with a water solution of a sulphate salt of an adherence enhancing metal chosen from a group consisting of cobalt and nickel, drying and heating the metal to decompose the salt and to form a thin coating of the adherence enhancing metal alloyed with the ironbr tee], the concentration of the solution being suc as to result in a final coating after full treatment of more than .02 gram and less than around .14 gram of the Y adherence enhancing metal per square foot of the surface of the pieces, and after- 'ward acid treating the pieces.
  • a process as claimed in claim 3 including also the step of reducing said pieces by rolling after the formation of the alloyed coating thereon.
  • a process for the purpose described which comprises coating iron or steel pieces with a sulphate salt of an adhesion promoting metal for enameling work, decomposing said salt on the surface of said pieces by a heat treatment whereby in part at least, an alloy of iron and the ad hesion promoting metal is produced, together with a compound of iron and sulphur, afterward reducingsaid pieces by rolling andflnally picksaid compound of iron and sulphur.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Heat Treatment Of Sheet Steel (AREA)
  • Metal Rolling (AREA)

Description

Patented Dec. 14,1937
UNITED STATES 2,101,950 PREPARING METAL FOR ENAMELING George W. McGohan, Middletown, Ohio, assign- L or to- The American Rolling Mill Company, Middletown, Ohio, a corporation 01' Ohio No Drawing. Continuation of application Serial- N0. 675,645, June 13, 1933. This application March 21, 1934, Serial No. 716,674
6 Claims. -(c1. 148-1) This is a continuation of my application of the same title, Serial No. 675,645, filed June 13, 1933.
My invention relates to providing an initial coating of metallic substance, comprising an adhesion promoting-metal, preferably nickel, on
iron and steel, and more particularly on sheet metal, was to prepare itfor enameling as with vitreous enamel. Y
' Among other things, my invention provides a 10 method of forming in the surface elements of a sheet or other piece of metal an extremely small thickness of coating which greatly assists in promoting adhesion of a subsequently applied coating of vitreous enamel. My method has the advantage of being subject to accurate control, and is admirably adapted to use at the rolling mill where the iron or steel sheets are prepared.
Sheets which are very low in carbon are recognized as the best for vitreous enameling, and while my method can be applied to steel of higher carbon content, the very low carbon is the best. Also,-although my coating is productive of most excellent bond of a first'coat of enamel even on a cold rolled high finish sheet, still if applied to a sheet which has been sand blasted or is roughened in-some other way, it will be easier to build up a first coat of desired thickness thereon prior to firing (of enamel).
While my method can be divided-into parts so that the final step may be carried out at the plant'of theenameler, yet, one of the'desirable features of my invention is that it is excellently adapted to being performed entirely at the rollingmill plant, since the surface effect is not interfered with by the pickling applied by the enameler for cleaning his metal prior to applying the first coat of enamel. Y
My method has the further advantageof' permitting the formation of the desired surface coat- 40 ing at various stages in the process of manufacturing the sheets themselves. Thus it is-possible usual way. I am-able thus to allocate the coat- -ing operation to any convenient point'in the processing sequence, and in particular to arrange to employ such heating stepor steps as form a part.
of the reduction process.
- One principle on which my invention isbased I 5.5 is my discovery that if a piece'of iron or steel compound.
is coated with a solution of a nickel salt, or the salt of some other metal which promotes adhesion in vitreous enameling, and heated high enough to convert the coating to a layer of the metal itself, or at least to a decomposable form 5 which will yield the metal itself, in subsequent processing steps it will yield an adherent and fixed coating which is believed to be formed of the adhesion promoting metal alloyed with the base'metal. Another principle on which my in- 10 vention is based is my discovery that my coating of nickel alloy or-the like is persistent through the ordinary reduction processes.
I shall first describe myinv'ention as a treatment applied to finished sheets, taking up here,- 1 inafter the other aspects'of my invention.
Thus, I may take an iron sheet and dip it in a solution of about 3 to 5% nickel sulphate, and then dry the sheet and raise it to a temperature of around 700 Fahr. or greater, with the result 2 of forming on the sheet a very thin coating of nickel, nickel iron alloy or at least of some nickel By subsequently picklingsthe sheet in a sulphuric acid pickling bath of usual iron and steel pickling concentration, I find that the nickel iron alloy is unaffected and/or any decomposable nickel compound is reduced, and/on'if reduction has already taken place, other undesirable reaction products are removed, as will hereinafter be 30 explained.
I have produced my product by dipping sheets in a 5% solution of nickel sulphate, then drying and heating at around 1l50 Fahr. I have also attained the desired results by normalizing at 35 1800 Fahn after. dipping but without necessity of drying, since the sheets are normalized individually and dry in'the furnace. A neutral or slightly reducing atmosphere seems to be desirable during the heating, and a highly oxidizing 40 flame is to be avoided, for reasons hereinafter made,clear. a
In my process I prefer to avoid plating out of any nickel from my original solution, because then I do not. have to keep adding nickel salt to 45 keep up the desired concentration, and all depos ited films of the nickel salt are substantially uniform. Moreover, a coating 'formedin my pro-. cedure differs in. important respects from a plated coating of nickel, electrically orchemically depos- 5o ited.
I I may apply the-sulphatesolution to a hotrolled sheet prior'to pickling-and only pickle the product once after the annealing. The thin scale does not seem to interfere with the treatment resulting in the formation of metallic nickel alloy on the surface of the sheet. I prefer, however, to pickle and remove the scale by washing the bars or other material from which the sheets are rolled and then proceed to the dipping in nickel sulphate solution prior to final rolling.
It will be clear that the heating step is an essential part of the process, for the purp se of decomposing the nickel salt. Not only would a coatin of nickel salt as such, 1. e., without the heating step, be lacking in ultimate adhesion, but it would be highly undesirable in the enameling step because of the setting-up effect of the nickel salt upon the enamel itself. When the pieces are heated in an atmosphere which is not highly oxidizing, and particularly in neutral or reducing atmospheres, a relatively strongly adherent coating is produced. I do not desire to be bound by theory; but I am led by my results to believe that unless the atmosphere of the furnace is extremely oxidizing, a chemical reactionoccurs between a nickel compound at some stage and the iron itself, involving a reduction of one or more nickel compounds to metallic nickel, which alloys or otherwise is joined to the surface of the iron. I have .reason to believe therefore, that a thin nickel iron alloy layer is formed at the surface, together with the production of considerable quantities of iron oxide and iron sulphide, instead of a nickel oxide layer. This conclusion appears to be supported by the following experimental evidence: A thin oxide layer formed by heating the treated iron piece to scaling temperature, as may be done during heating for rolling, or during annealing, appears to' consist essentially entirely of iron oxide with very little, if any, nickel oxide. Too, it is impossible by scrubbing or the like to remove any appreciable proportions of the nickel. Sandblasting of the sheet surface fails to remove the nickel, while grinding with abrasion wheels does remove it. While I therefore believe that a true nickel-iron alloy is produced, yet where I use the term "alloy I desire to be understood as referring to the result produced by following my process, irrespective of the correctness of the theoretical explanation which'I have advanced.
} An ultimate pickling step is of importance, not only to possibly effect the reduction of any nickel compounds which persist but also to remove the iron sulphide produced as I have indicated above.
' and to clean the sheet. It is to be noted, however,
that this pickling need not immediately follow the heat treatment, but may be any pickling which is incident to the process of producing sheets at the rolling mill, or may even be, as I have indicated above, the usual pickling applied to the sheets by the enameler.
I have discovered as indicated, that coatings of nickel or the like may be produced on pieces for rolling, such as sheet bars, rough plate or thin bars,-by the steps of coating with the salt of the coating metal, followed by a heat treatment,
. with or without a pickling, and that such coatings will be persistent throughout subsequent sheet reducing operations.
For example, in following a hot reduction method, thin bars, produced as usual on the roughing mill, are preferably pickled to obtain. a clean surface which will be easily wet. -The pickled thin bars are then wetted with a nickel solution, preferably by running them between rag I rolls soakedwith the solution, whereupon they may or may not be dried. They are then heated for hot reduction of thickness in the usual manner and are processed according to the ordinary veniently be located in the production line. 01-.-
dinarily, finished sheets will be given anannealing'.
It has been pointed out above that in so far as a heat treatment results in scaling, the scale will be found to consist almost entirely of iron. Consequently, the usual annealing treatment is not destructive of 'my coating. .The annealing is usually followed by a pickling, and the effects of this pickling have been outlined above.
In 'the exemplary cold reduction method,
pickled thin bars are coated as described, and then are heated in a furnace at approximately 1000 to 1500 Fahr., which forms the nickel alloy on the surface of the bars. The bars'are afterward cooled and reduced to sheets by cold rolling methods as usually practiced in the art. In this exemplary process the heating of the thin bars is, of course, an extra operation, but is necessary for reasons which will be clear from thelforegoing explanation. The heating at'approximately 1000 to 1500 Fahr. forms a thin gray-blue oxide on the sheets, which is very tightly adhering. The heating forms'the nickel alloy in the surface elements of the sheet or bar so that it is not removed during the cold reduction. The scale which I have Just described, does not appear to have any detrimental effect upon the rolls in the cold mills, and it has the advantage of providing an ultimate pickled sheet the surfaces of which are alloyed with nickel and are also slightly roughened. This likewise promotes adhesion of the enamel.
It has been found by experience that the optimum concentration of nickel sulphate is approximately 55 to 60 grams of nickel sulphate (NiSO4.6H2O) per cc. of solution, applied to rolling pieces of twice the final thickness.
It will be understood, in these specifications, where I employ such terms as nickel coating, decomposable substance, oxide layer, nickel-iron alloy, etc., that I do not use these expressions in a limiting sense, but desire them to be understood, in the light of the explanations which I have given hereinabove, as referring to such coatings as produce the surface effect resulting from the teachings set forth in these specifications.
tained. The desirable. thickness of nickel deposit according to my investigation is between '.03 and .10 gram per square foot of surface as determined by chemical analysis. It can be regulated by controlling the concentration of nickel sulphate solution in which the sheet is initially dipped. A suitable dried film of nickel sulphate [weighing from .14 gram per square foot to .46
gram per square foot of surface, will serve the purpose; but my invention is not limited by these figures. I have, for example, secured excellent results by treating thin bar with the concentration of .nickel solution given above, so as to produpe a bar having .07 to .10 gram of metallic So far as I have been able to determine, any
type of annealing of the metal sheet will serve as the heat treatment necessary to decompose the salt originally deposited on the sheet.
A cobalt flashing can be applied by following my method, also other salts than the sulphate salt of adhesion promoting metals can be used but I preferably employ nickel sulphate because it is quite inexpensive.
It is practical, instead of giving a pickle to the heat-treated product directly, to ship the product with the resulting film upon it, and have the enameler pickle it.
The product in sheet form may be shipped to the enameler and by him formed into shape, followed by the usual pickling and cleaning methods, without interfering with the effectiveness of the coating.
Having thus described my invention, what I claim as new and desire to secure by Letters Patent, is:--
1. A process of preparing iron or steel for vitreous enameling which consists in coating the metal with a heat decomposable salt of an adherence enhancing metal, heating the metal to decompose the salt and form a thin coating of the adherence enhancing metal alloyed with the iron or steel and'acid treating the product, said metal being nickel.
2. A process for the purposedescribed which comprises coating iron or steel pieces with a sulphate salt of an adhesion promoting metal for enameling work, decomposing said salt on the surface of said pieces by a heat treatment whereby in part at least, an alloy of iron and the adhesion promoting metal is'produced, together By the term sheet with a compound or iron and sulphur, and alterward pickling said pieces sufllciently at ieast to decompose said compound of iron and sulphur.
3. A process of preparing iron or steel for vitreous enameling, which comprises dipping iron or steel pieces in awate'r solution of a. heat decomposable'salt of an adherence enhancing metal chosen from a group consisting of cobalt and nickel, and drying and heating the metal to decompose the salt and form a thin coating of the adherence enhancing metal alloyedwith the iron or steel, afterward acid treating said pieces.
4. A process 'of preparing iron or steel for vitreous enamelingwhich comprises coating iron or steel pieces with a water solution of a sulphate salt of an adherence enhancing metal chosen from a group consisting of cobalt and nickel, drying and heating the metal to decompose the salt and to form a thin coating of the adherence enhancing metal alloyed with the ironbr tee], the concentration of the solution being suc as to result in a final coating after full treatment of more than .02 gram and less than around .14 gram of the Y adherence enhancing metal per square foot of the surface of the pieces, and after- 'ward acid treating the pieces.
5. A process as claimed in claim 3 including also the step of reducing said pieces by rolling after the formation of the alloyed coating thereon.
6. A process for the purpose described which comprises coating iron or steel pieces with a sulphate salt of an adhesion promoting metal for enameling work, decomposing said salt on the surface of said pieces by a heat treatment whereby in part at least, an alloy of iron and the ad hesion promoting metal is produced, together with a compound of iron and sulphur, afterward reducingsaid pieces by rolling andflnally picksaid compound of iron and sulphur.
' ling said pieces sufllciently at least to decompose GEORGE w. MCGOHAN.
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Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2421719A (en) * 1942-06-06 1947-06-03 Western Electric Co Vitreous enamelled article
US2495762A (en) * 1945-06-04 1950-01-31 George N Hibben Enameled article
US2495835A (en) * 1945-10-15 1950-01-31 George N Hibben Light-colored enameled steel article
US2510071A (en) * 1945-08-09 1950-06-06 Poor & Co Vitreous enameling of ferrous metal
US2581310A (en) * 1951-11-06 1952-01-01 Ferro Corp Porcelain enamel article and method of producing same
US2639264A (en) * 1949-04-13 1953-05-19 Poor & Co Vitreous enameling processes and products
US2650903A (en) * 1947-07-05 1953-09-01 Westinghouse Electric Corp Protection of molybdenum against oxidation
US2662270A (en) * 1943-07-01 1953-12-15 Olin Ind Inc Manufacture of laminated structures
US2695249A (en) * 1950-04-05 1954-11-23 Ferro Corp Porcelain enamel article and method of making same
US2755210A (en) * 1949-06-25 1956-07-17 Armco Steel Corp Method of treating iron or mild steel to promote the adherence of porcelain enamel, and stock so produced
US2768904A (en) * 1946-08-09 1956-10-30 Poor & Co Vitreous enameling process
US2819207A (en) * 1953-06-22 1958-01-07 Republic Steel Corp Process for enameling steel
US2975072A (en) * 1958-12-09 1961-03-14 Ferro Corp Protective coatings for combustion engine exhaust systems
US3468724A (en) * 1966-03-31 1969-09-23 Amchem Prod Metal coating process
US3911177A (en) * 1972-05-16 1975-10-07 Cockerill Process for preparing steel for enameling

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2421719A (en) * 1942-06-06 1947-06-03 Western Electric Co Vitreous enamelled article
US2662270A (en) * 1943-07-01 1953-12-15 Olin Ind Inc Manufacture of laminated structures
US2495762A (en) * 1945-06-04 1950-01-31 George N Hibben Enameled article
US2510071A (en) * 1945-08-09 1950-06-06 Poor & Co Vitreous enameling of ferrous metal
US2495835A (en) * 1945-10-15 1950-01-31 George N Hibben Light-colored enameled steel article
US2768904A (en) * 1946-08-09 1956-10-30 Poor & Co Vitreous enameling process
US2963784A (en) * 1946-08-09 1960-12-13 Poor & Co Base stock for vitreous enamel coatings
US2650903A (en) * 1947-07-05 1953-09-01 Westinghouse Electric Corp Protection of molybdenum against oxidation
US2639264A (en) * 1949-04-13 1953-05-19 Poor & Co Vitreous enameling processes and products
US2755210A (en) * 1949-06-25 1956-07-17 Armco Steel Corp Method of treating iron or mild steel to promote the adherence of porcelain enamel, and stock so produced
US2695249A (en) * 1950-04-05 1954-11-23 Ferro Corp Porcelain enamel article and method of making same
US2581310A (en) * 1951-11-06 1952-01-01 Ferro Corp Porcelain enamel article and method of producing same
US2819207A (en) * 1953-06-22 1958-01-07 Republic Steel Corp Process for enameling steel
US2975072A (en) * 1958-12-09 1961-03-14 Ferro Corp Protective coatings for combustion engine exhaust systems
US3468724A (en) * 1966-03-31 1969-09-23 Amchem Prod Metal coating process
US3911177A (en) * 1972-05-16 1975-10-07 Cockerill Process for preparing steel for enameling

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