US2301741A - Coating of metal surfaces - Google Patents
Coating of metal surfaces Download PDFInfo
- Publication number
- US2301741A US2301741A US334265A US33426540A US2301741A US 2301741 A US2301741 A US 2301741A US 334265 A US334265 A US 334265A US 33426540 A US33426540 A US 33426540A US 2301741 A US2301741 A US 2301741A
- Authority
- US
- United States
- Prior art keywords
- enamel
- coating
- metal
- glass
- milled
- 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
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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
- C23D—ENAMELLING OF, OR APPLYING A VITREOUS LAYER TO, METALS
- C23D5/00—Coating with enamels or vitreous layers
- C23D5/02—Coating with enamels or vitreous layers by wet methods
Definitions
- This invention relates to-a process for coating metallic surfaces, specifically ferrous metal surfaces, with a vitreous and fused enamel coating and bonding the same to the metallic surface.
- A' further object of my invention is to provide a process of the character referred to which'involves the use of agents or materials which, when used in accordance with the process of the present invention, operate to control the bond of the vitreous coating, to the ferrous metal surface, by controlling the nature and quantity of the nascent iron oxide produced during fusion,
- a further and important object of the invention is to employ vitreous combinations having fusion points lower than the fusion points of sheet steel enamel ground or grip coats, thereby permitting the present invention to be carried-out in connection with lighter gauge metal sheets and with a wider range of base metal compositions than heretofore possible.
- Feldspathic, or metallic borosilicates having fusion points in the range of 1000 F. to 1250 F. do not have sufllclent adherence, when milled, sprayed, and fused on ferrous metal surfaces, to be used as decorative or corrosion resisting films without the preceding application of a higher firing ground or grip coat of the conventional cobalt, nickel and manganese wet-process enamel type.
- the addition to the mill or milled slip of an oxidizing agent, such as ferric sulphate, decomposing below the fusion temperature of the glass and forming stable decomposition products compatible with the vitreous body aids in bonding these glasses to low carbon enamelling iron or steel, and in particular to those ferrous alloys slightly higher in silicon, phosphorus and manganese and known commercially as hot rolled steel.
- an oxidizing agent such as ferric sulphate
- the coated metal is fired in an oxidizing amples of high lead borosilicate glasses with which the present process is particularly applicable:
- Such high lead borosilicate glasses fuse at temperatures in the range of 1000" F. to 1260 F.
- Frit-.. pounds 100 Bentoniite ounces 4 Ilmenite do 6 Black iron oxide dO. 4 Water pounds 40 The above is to give a medium gray mill; the color may be changed by changing the oxide addition at the mill.
- a distinctive feature of the present invention is to utilize with these glass or frit formulae an oxidizing agent compatible with the glass, such as ferric sulphate, as a further addition which acts atmosphere which is below 1260 F. Below this temperature there is no danger of warpage, strain and softening of the steel. With this process 30 gauge steel has been and is being successfully coated without warpage of the steel or hair-lining or crazing of the vitreous enamel coating.-
- an oxidizing agent compatible with the glass such as ferric sulphate
- the present invention can be used successfully with several glass or enamel frit formulae, and for purposes ofthe present application two such formulae may be given as ex* as an agent to cause the fused glass or porcelain' to be bonded to the ferrousmetal surface over which it has been previously applied.
- Another oxidizing agent compatible with glasses of the type mentioned, and which may be advantageously employed in the process of the present invention is sodium nitrite, which may be added to the milled slip containing ferric sulphate in the proposition of 1. cubic centimeter of a aqueous solution to 100 cubic centimeters of milled slip.
- the process may be further explained by stating that, at the low fusion temperatures employed, insufficient iron oxide is produced thenmally and dissolved by the molten glass body to 20 provide for a mutually soluble iron-glass interlocking layer between the vitreous coating and the base metal.
- the quantity of the nascent iron oxide produced is increased sufficiently to insure adequate adherence.
- ferric sulphate as the oxidizing agent provides both additional iron oxide for solution in the melt, and
- the raw materials for the enamel are mixed and smelted This fritted preferably to a fineness of 3-7% residue on a 200 0 mesh screen from a 100 gram sample.
- The20% solution of ferric sulphate is then added in the proportion of one part of sulphate solution to each one hundred parts by volume of milled slip,
- sodium nitrite 'is to be used as an auxiliary oxidizing agent it is added in the proportion of 1 cc. of a 20% aqueous solution to cc. of milled slip containing the sulphate solution. This proportion may be varied somewhat for some irons or steels, and some glasses.
- the metal articles to be coated are first cleaned, using commercial alkaline cleaning materials, then rinsed, pickled in acid, r1nsed,, neutralized and dried. Sand blasting may be substituted for cleaning and pickling in case of heavier gauge metals or cast iron.
- the metal article is then coated with th neamel slip, either by sprayin dipping; slushin or other known means; dried to remove moisture, and then fired at the proper temperature, which may be at 1070 F. for Example I and 1120 F. for Example 11. In any case, the upper limit of the temperature range does not exceed 1260 R, thereby avoiding warpage and other physical change in the metal being coated.
- oxidizing agents decomposing below a temperature of 1200" E and forming stable decomposition products compatible with the em amels used in the present process are ferric chloride, potassium dichromate, sodium dichromate, and sodium sulphate.
- mild alkali usually consisting of mixtures of sodium carbonate and borax in varying amounts
- phosphates or other water softeners are used. More specifically, there is a mixture of three parts of soda ash and one part of borax by weight in a total concentration of one-fourth ounce per gallon. The solution is used at F. and the time of immersion is approximately four minutes.
- the new step of applying to the metal sheet a, self-bonding milled slip containing a metallic boro-silicate having a fusing point in the range of 1000 F. to 1260 F. and a solution of ferric .sulphate decomposable below the fusion temperature of the glass.
- the new step of applying to the metal sheet a self-bonding milled slip containing a metallic born-silicate having a fusing. point in the range of 1000 F. to 1260 F. and a solution of ferric sulphate and sodium nitrite.
- a process of preparing a self-bonding enamel or glass composition for use in enamel-coating processes which consists in first preparing a lead boro-silicate glass frit having a fusing temperature in the range of 1000 F. to 1260" F., reducing the said frit to a milled slip, and then incorporating in said milled slip a solution of ferric sulphate.
- a process of preparing a self-bonding enamel or glass composition for use in enamel-coating processes which consists in first preparing a lead boro-silicate glass frit having a fusing temperature in the range of 1000 F. to 1260 F., re-
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Glass Compositions (AREA)
- Laminated Bodies (AREA)
Description
Patented Nov. 10, 1942 COATING OF METAL SURFACES William Collins Morris, North Chicago, Ill.) assignor to Poor a Company, Chicago, 111., a corporationof Delaware No Drawing. Application May 9, 1940, Serial No. 334,265
4 Claims.
This invention relates to-a process for coating metallic surfaces, specifically ferrous metal surfaces, with a vitreous and fused enamel coating and bonding the same to the metallic surface.
A' further object of my invention is to provide a process of the character referred to which'involves the use of agents or materials which, when used in accordance with the process of the present invention, operate to control the bond of the vitreous coating, to the ferrous metal surface, by controlling the nature and quantity of the nascent iron oxide produced during fusion,
A further and important object of the invention is to employ vitreous combinations having fusion points lower than the fusion points of sheet steel enamel ground or grip coats, thereby permitting the present invention to be carried-out in connection with lighter gauge metal sheets and with a wider range of base metal compositions than heretofore possible.
Feldspathic, or metallic borosilicates, having fusion points in the range of 1000 F. to 1250 F. do not have sufllclent adherence, when milled, sprayed, and fused on ferrous metal surfaces, to be used as decorative or corrosion resisting films without the preceding application of a higher firing ground or grip coat of the conventional cobalt, nickel and manganese wet-process enamel type. Whereas, according to the present invention, the addition to the mill or milled slip of an oxidizing agent, such as ferric sulphate, decomposing below the fusion temperature of the glass and forming stable decomposition products compatible with the vitreous body, aids in bonding these glasses to low carbon enamelling iron or steel, and in particular to those ferrous alloys slightly higher in silicon, phosphorus and manganese and known commercially as hot rolled steel.
Though it is necessary with enamel glasses firing on ferrous metal surfaces at the usual temperature ranges of 1500 F. to 1650 F. to use electric furnaces or fuel fired full muflle furnaces to insure burning atmospheres free from'the prodcts of combustion, however, according to the resent invention, it is possible to utilize direct red fuel furnaces, thereby materially decreasing equipment costs and operating expenses.
That is to say, according to the present invention, the coated metal is fired in an oxidizing amples of high lead borosilicate glasses with which the present process is particularly applicable:
Such high lead borosilicate glasses fuse at temperatures in the range of 1000" F. to 1260 F.
The mill additions for either Formula I or Formula II would be:
Frit-.. pounds 100 Bentoniite ounces 4 Ilmenite do 6 Black iron oxide dO. 4 Water pounds 40 The above is to give a medium gray mill; the color may be changed by changing the oxide addition at the mill.
A distinctive feature of the present invention is to utilize with these glass or frit formulae an oxidizing agent compatible with the glass, such as ferric sulphate, as a further addition which acts atmosphere which is below 1260 F. Below this temperature there is no danger of warpage, strain and softening of the steel. With this process 30 gauge steel has been and is being successfully coated without warpage of the steel or hair-lining or crazing of the vitreous enamel coating.-
Furthermore, the present invention can be used successfully with several glass or enamel frit formulae, and for purposes ofthe present application two such formulae may be given as ex* as an agent to cause the fused glass or porcelain' to be bonded to the ferrousmetal surface over which it has been previously applied.
With normal hot rolled black iron as purchased from steel mills, it is found that the addition of to 1% cubic centimeters of a 20% aqueous solution .of ferric sulphate to cubic centimeters of milled slip of a high lead borosilicate glass having a specific gravity of 1.95
to 3.05, bonds this material to the metal surface when the metal is sprayed with this mixed slip and fired to a maturing temperature. This can be used with the -frit of either Formula I or Formula II.
After the frit of Formula I or Formula II, with mill additions, is milled to appropriate fineness, it is measured and a 20% aqueous solution of ferric sulphate is added in the proportions of one part of sulphate solution to each one hundred parts by volume of milled slip. For some steels and some glasses different proportions of ferric sulphate will be found to work more satisfactorily.
Another oxidizing agent compatible with glasses of the type mentioned, and which may be advantageously employed in the process of the present invention, is sodium nitrite, which may be added to the milled slip containing ferric sulphate in the proposition of 1. cubic centimeter of a aqueous solution to 100 cubic centimeters of milled slip.
Two steels which were found to work very satisfactory with the ferric sulphate-enamel slip mixture described above had the following analysis:
I Ii
o. 050 0. 032 o. 420 o. 440 o. 040 0. can 0. 027 0. 03s 0. 100 0. 21s 0. 061 0.003
The process may be further explained by stating that, at the low fusion temperatures employed, insufficient iron oxide is produced thenmally and dissolved by the molten glass body to 20 provide for a mutually soluble iron-glass interlocking layer between the vitreous coating and the base metal. For example, the metallic boro= silicates, or majolica types of enamels, given in Formula I and Formula H are so strongly re- 25 ducing in nature when fluid that when fired upon hot rolled steel at temperatures from 1000"" F. to 1260" F. they have no adherence whatever. The surface'of the steel exposed upon removing such glasses from the metal is white and clean, show= ing no indication of thermal oxidation during fusion. However, by the addition of an omdizing agent which decomposes below the firing point of the enamel, and which does not form stable decomposition products harmful to the vitreous body, the quantity of the nascent iron oxide produced is increased sufficiently to insure adequate adherence. In particular, the addition of ferric sulphate as the oxidizing agent provides both additional iron oxide for solution in the melt, and
a transitory oxidizing state at the interface of the enamel and the iron before fusion of the glass is complete. The necessary quantity of oxidiaing agent is dependent upon the oxidizing char= acteristics of the steel, the chemical nature of the melt at the interface, and the quantity of iron oxide soluble in the ceramic composition being used.
Taking one phase of the process, the raw materials for the enamel are mixed and smelted This fritted preferably to a fineness of 3-7% residue on a 200 0 mesh screen from a 100 gram sample. The20% solution of ferric sulphate is then added in the proportion of one part of sulphate solution to each one hundred parts by volume of milled slip,
and if sodium nitrite 'is to be used as an auxiliary oxidizing agent it is added in the proportion of 1 cc. of a 20% aqueous solution to cc. of milled slip containing the sulphate solution. This proportion may be varied somewhat for some irons or steels, and some glasses.
The metal articles to be coated are first cleaned, using commercial alkaline cleaning materials, then rinsed, pickled in acid, r1nsed,, neutralized and dried. Sand blasting may be substituted for cleaning and pickling in case of heavier gauge metals or cast iron. The metal article is then coated with th neamel slip, either by sprayin dipping; slushin or other known means; dried to remove moisture, and then fired at the proper temperature, which may be at 1070 F. for Example I and 1120 F. for Example 11. In any case, the upper limit of the temperature range does not exceed 1260 R, thereby avoiding warpage and other physical change in the metal being coated.
ifither oxidizing agents decomposing below a temperature of 1200" E, and forming stable decomposition products compatible with the em amels used in the present process are ferric chloride, potassium dichromate, sodium dichromate, and sodium sulphate.
By way of definition of certain terms employed herein it may be explained that the reference to neutralizing the rinsed metal articles preferably means immersion in a warm bath of mild alkali usually consisting of mixtures of sodium carbonate and borax in varying amounts, the total con= centration being in general less than one ounce per gallon. In some cases where the water is extremely hard, phosphates or other water softeners are used. More specifically, there is a mixture of three parts of soda ash and one part of borax by weight in a total concentration of one-fourth ounce per gallon. The solution is used at F. and the time of immersion is approximately four minutes.
It will be further understood that modifications in the process, materials employed, and the formulae thereof, proportions of ingredients and temperature ranges, falling within the scope of the appended claims 'may be resorted to without departing from the spirit or scope'of the inven tion.
I claim:
1. In the process of enamel-coating ferrous metals, the new step of applying to the metal sheet a, self-bonding milled slip containing a metallic boro-silicate having a fusing point in the range of 1000 F. to 1260 F. and a solution of ferric .sulphate decomposable below the fusion temperature of the glass.
2. In the process of enamel-coating ferrous metals, the new step of applying to the metal sheet a self-bonding milled slip containing a metallic born-silicate having a fusing. point in the range of 1000 F. to 1260 F. and a solution of ferric sulphate and sodium nitrite.
3. A process of preparing a self-bonding enamel or glass composition for use in enamel-coating processes which consists in first preparing a lead boro-silicate glass frit having a fusing temperature in the range of 1000 F. to 1260" F., reducing the said frit to a milled slip, and then incorporating in said milled slip a solution of ferric sulphate.
4. A process of preparing a self-bonding enamel or glass composition for use in enamel-coating processes which consists in first preparing a lead boro-silicate glass frit having a fusing temperature in the range of 1000 F. to 1260 F., re-
ducing the said frit to a milled slip, and then insulphate and sodium nitrite.
WILLIAM COLLINS MORRIS.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US334265A US2301741A (en) | 1940-05-09 | 1940-05-09 | Coating of metal surfaces |
GB31108/47A GB634262A (en) | 1940-05-09 | 1947-11-24 | Improvement in coating of metal surfaces |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US334265A US2301741A (en) | 1940-05-09 | 1940-05-09 | Coating of metal surfaces |
Publications (1)
Publication Number | Publication Date |
---|---|
US2301741A true US2301741A (en) | 1942-11-10 |
Family
ID=23306402
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US334265A Expired - Lifetime US2301741A (en) | 1940-05-09 | 1940-05-09 | Coating of metal surfaces |
Country Status (2)
Country | Link |
---|---|
US (1) | US2301741A (en) |
GB (1) | GB634262A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2457678A (en) * | 1944-07-13 | 1948-12-28 | Continental Carbon Inc | Resistor and method of making |
US2554373A (en) * | 1947-06-16 | 1951-05-22 | Usines Chimiques Rhone Poulene | Process for producing glossy coatings on earthenware and metal |
US2786307A (en) * | 1953-05-18 | 1957-03-26 | Owens Illinois Glass Co | Method of making glass-to-metal seals |
US2786782A (en) * | 1954-08-31 | 1957-03-26 | Haven M Zimmerman | Enameling ground-coat composition and process of application thereof |
US2919210A (en) * | 1956-11-07 | 1959-12-29 | Owens Illinois Glass Co | Method of applying glass forming metal borates to surfaces |
US2963805A (en) * | 1957-09-03 | 1960-12-13 | Boeing Co | Porcelain enameled foil labels |
-
1940
- 1940-05-09 US US334265A patent/US2301741A/en not_active Expired - Lifetime
-
1947
- 1947-11-24 GB GB31108/47A patent/GB634262A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2457678A (en) * | 1944-07-13 | 1948-12-28 | Continental Carbon Inc | Resistor and method of making |
US2554373A (en) * | 1947-06-16 | 1951-05-22 | Usines Chimiques Rhone Poulene | Process for producing glossy coatings on earthenware and metal |
US2786307A (en) * | 1953-05-18 | 1957-03-26 | Owens Illinois Glass Co | Method of making glass-to-metal seals |
US2786782A (en) * | 1954-08-31 | 1957-03-26 | Haven M Zimmerman | Enameling ground-coat composition and process of application thereof |
US2919210A (en) * | 1956-11-07 | 1959-12-29 | Owens Illinois Glass Co | Method of applying glass forming metal borates to surfaces |
US2963805A (en) * | 1957-09-03 | 1960-12-13 | Boeing Co | Porcelain enameled foil labels |
Also Published As
Publication number | Publication date |
---|---|
GB634262A (en) | 1950-03-15 |
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