US2581310A - Porcelain enamel article and method of producing same - Google Patents
Porcelain enamel article and method of producing same Download PDFInfo
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- US2581310A US2581310A US255130A US25513051A US2581310A US 2581310 A US2581310 A US 2581310A US 255130 A US255130 A US 255130A US 25513051 A US25513051 A US 25513051A US 2581310 A US2581310 A US 2581310A
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- United States
- Prior art keywords
- work piece
- nickel
- steel
- enamel
- solution
- Prior art date
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- 238000000034 method Methods 0.000 title claims description 54
- 239000000037 vitreous enamel Substances 0.000 title claims description 24
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical class [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 142
- 229910000831 Steel Inorganic materials 0.000 claims description 49
- 239000010959 steel Substances 0.000 claims description 49
- 230000008569 process Effects 0.000 claims description 31
- 210000003298 dental enamel Anatomy 0.000 claims description 29
- 239000000243 solution Substances 0.000 claims description 29
- 239000011248 coating agent Substances 0.000 claims description 15
- 238000000576 coating method Methods 0.000 claims description 15
- 239000003638 chemical reducing agent Substances 0.000 claims description 14
- 239000007864 aqueous solution Substances 0.000 claims description 13
- 238000010304 firing Methods 0.000 claims description 9
- 238000005342 ion exchange Methods 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 7
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 claims description 7
- 230000001737 promoting effect Effects 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 229910052759 nickel Inorganic materials 0.000 description 70
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 17
- 238000005554 pickling Methods 0.000 description 14
- 229910052573 porcelain Inorganic materials 0.000 description 14
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 13
- 229910017604 nitric acid Inorganic materials 0.000 description 13
- 150000002815 nickel Chemical class 0.000 description 12
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 10
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 10
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 10
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 9
- 239000001632 sodium acetate Substances 0.000 description 9
- 235000017281 sodium acetate Nutrition 0.000 description 9
- 230000009471 action Effects 0.000 description 8
- 238000000151 deposition Methods 0.000 description 8
- KWSLGOVYXMQPPX-UHFFFAOYSA-N 5-[3-(trifluoromethyl)phenyl]-2h-tetrazole Chemical compound FC(F)(F)C1=CC=CC(C2=NNN=N2)=C1 KWSLGOVYXMQPPX-UHFFFAOYSA-N 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 229910001379 sodium hypophosphite Inorganic materials 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 230000008021 deposition Effects 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 5
- 238000004140 cleaning Methods 0.000 description 5
- 238000004534 enameling Methods 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 5
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 description 5
- 238000006722 reduction reaction Methods 0.000 description 5
- 125000002091 cationic group Chemical group 0.000 description 4
- GQZXNSPRSGFJLY-UHFFFAOYSA-N hydroxyphosphanone Chemical compound OP=O GQZXNSPRSGFJLY-UHFFFAOYSA-N 0.000 description 4
- 229940046817 hypophosphorus acid Drugs 0.000 description 4
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 4
- 239000007800 oxidant agent Substances 0.000 description 4
- 238000007747 plating Methods 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 238000007788 roughening Methods 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 239000010960 cold rolled steel Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000001117 sulphuric acid Substances 0.000 description 3
- 235000011149 sulphuric acid Nutrition 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- BZSXEZOLBIJVQK-UHFFFAOYSA-N 2-methylsulfonylbenzoic acid Chemical compound CS(=O)(=O)C1=CC=CC=C1C(O)=O BZSXEZOLBIJVQK-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 239000010953 base metal Substances 0.000 description 2
- 229910052793 cadmium Inorganic materials 0.000 description 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- -1 dirt Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000004519 grease Substances 0.000 description 2
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000005488 sandblasting Methods 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- 238000003466 welding Methods 0.000 description 2
- XXSPKSHUSWQAIZ-UHFFFAOYSA-L 36026-88-7 Chemical compound [Ni+2].[O-]P=O.[O-]P=O XXSPKSHUSWQAIZ-UHFFFAOYSA-L 0.000 description 1
- 241000271039 Agkistrodon Species 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910001377 aluminum hypophosphite Inorganic materials 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229910001610 cryolite Inorganic materials 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000010433 feldspar Substances 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 159000000014 iron salts Chemical class 0.000 description 1
- 229910001381 magnesium hypophosphite Inorganic materials 0.000 description 1
- SEQVSYFEKVIYCP-UHFFFAOYSA-L magnesium hypophosphite Chemical compound [Mg+2].[O-]P=O.[O-]P=O SEQVSYFEKVIYCP-UHFFFAOYSA-L 0.000 description 1
- FLFJVPPJGJSHMF-UHFFFAOYSA-L manganese hypophosphite Chemical compound [Mn+2].[O-]P=O.[O-]P=O FLFJVPPJGJSHMF-UHFFFAOYSA-L 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 235000021110 pickles Nutrition 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
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
- C23C18/00—Chemical 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
- C23C18/16—Chemical 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 reduction or substitution, e.g. electroless plating
- C23C18/31—Coating with metals
- C23C18/32—Coating with nickel, cobalt or mixtures thereof with phosphorus or boron
- C23C18/34—Coating with nickel, cobalt or mixtures thereof with phosphorus or boron using reducing agents
- C23C18/36—Coating with nickel, cobalt or mixtures thereof with phosphorus or boron using reducing agents using hypophosphites
-
- 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
- C23D3/00—Chemical treatment of the metal surfaces prior to coating
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9335—Product by special process
- Y10S428/936—Chemical deposition, e.g. electroless plating
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9335—Product by special process
- Y10S428/939—Molten or fused coating
Definitions
- This invention relates, as indicated, to per.- celain enameling and has more particular reference to an enameling procedure and articles produced therefrom characterized by the direct application to a steel surface of porcelain enamel of the type ordinarily referred to. as cover coat porcelain enamel in that it does not contain any substantial amounts of those materials, such as oxides of cobalt and nickel for example, which have heretofore been deemed necessary in order to insure satisfactory adherence between the enamel and the steel.
- this invention comprises the method of porcelain enamelling a steel work piece which comprises cleaning and roughening the surface of the work piece so as to produce a surface condition characterized by deep sharp edged pits therein characteristic of the surface resulting from pickling with an aqueous solution of nitric acid, immersing said roughened steel work piece in an aqueous solution of a nickel salt, said solution containing a.
- reducing agent selected from the class consisting of hypophosphorous acid and those salts thereof, the cationic portion of which is above tin in the electromotive series whereby when the steel work piece is immersed in said solution the nickel salt is reduced and nickel deposited on the work piece without ion exchange between the work piece and the solution, maintaining the work piece in said solution until there has been deposited on the roughened surface thereof from about .04 to about .25 grams per square foot of nickel coating thereon, washing and drying the work piece, then applying directly on the thus nickelcoated roughened surface of the work piece a cover coat porcelain enamel which is substantially free of adherence promoting oxides, and then firing such enamel thereon.
- the steel surface to which the porcelain enamel is to be eventually applied when practicing my invention needs to have two primary characteristics. First, it must be relatively clean, that is free from all foreign materials such as dirt, grease and the usual coat of metallic oxide. Second the surface of the steel must be reasonably rough for best adherence of the porcelain enamel. This preparation of the steel surface may be accomplished by chemical means or by mechanical means or by a combination of the two. If it is desirable to effect the preparation of the surface by chemical means only, this can be accomplished conveniently by the use of pickling baths which leave a relatively rough surface.
- the pickling baths which are available for this purposes are, for example those employing nitric acid and combinations of nitric acid with other acids and baths which are primarily sulphuric acid baths, but which also contain nitric acid or other oxidizing agents.
- This type of bath has two principal characteristics. First the bath is extremely vigorous in its action so that the required pickling time is relatively short and second, this type of bath produces a surface which may be identified, for convenience, as a deeply etched surface, in that it contains pits which are relatively deep with the crests between such pits relatively sharp. Because of this peculiar type of surface just described which is produced by pickling baths of the type ust described they are preferred for use in my process since it has been found that adherence between the enamel and the steel is greatest when the steel surface is thus preliminarily prepared.
- All of the various pickling processes referred to above are capable of producing; the roughened surface on the work which is characterized by deep sharp-edged pits therein.
- This type of surface preferably is produced by means of a pickling solution which is an aqueous solution of nitric acid containing about one part of concentrated nitric acid to each four parts oi; water.
- a satisfactory surface will usually be produced in about one minute at room temperature. As the temperature increases the time is accordinghr reduced.
- Typical examples of sulphuric acid baths containing oxidizing agents which are effective to produce a surface characterized by deep sharp-edged pits therein will depend not only on the temperature of the bath, but also on the relative concentrations of sulfuric acid and oxldizng agent.
- the sodium chlorate bath given above will usually produce a satisfactory surface, when operated at 160 F. temperature, for 3 minutes.
- the sulfuric acid bath utilizing nitric acid as the oxidizing agent as given above when operated at F. temperature will produce a satisfactory result in about 3 minutes.
- NICKEL DEPOSITIONS The nickel flash method previously referred to, i. e. the process for the deposition of nickel which depends upon galvanic action by the work piece and the bath has not been satisfactory for use in my process. It is believed that one reason why deposition of the nickel by galvanic action does not give satisfactory results is not only the inconsistency of that process and the variations in the deposits resulting therefrom, but also the nature of character of the nickel deposit resulting from such process. Since the very nature of the process is galvani this requires that there be a certain area of the steel surface always exposed to the action of the bath if the galvanic process is to proceed.
- the nickel layer thus laid down by the galvanic process is not what may be termed a uniform or substantially continuous layer of nickel. Instead it is a coating of nickel which is interrupted by areas wherein the base metal is exposed or only superficially coated.
- the nickel coating deposit be substantially uniform while at the same time permitting the occurrence of at least a minor amount of iron, in' free or combined form, at the bond.
- the process of depositing nickel by means of an electrolytic bath will produce a substantially continuous layer of nickel but such process is unsatisfactory for a number of reasons. First it can be used successfully only on simple shapes suchas flat sheets because if the article treated has any substantial contour deviating from a fiat plane there will be sufficient variation in the thickness of the nickel deposited on the various areas of the article to produce best results. Since the nature of the nickel deposit, 1.
- the thickness of the coat on the high points for example, will be sufllciently different from the thickness of the coat on the low points for example, so that if the coating at one place is adjusted to the narrower range for best results, the coating on the other area will be outside of such range.
- the process of depositing the nickel electrolytically can be used satisfactorily only on flat surfaces such as unfabricated steel sheets and strips and even on such surfaces the character of the deposit laid down by the electrolytic method is sufliciently different from the character of the deposits laid down by a chemical reduction method that it is not possible to secure the high order of adherence with the electrolytic process as it is with the process wherein the nickel is laid down by chemical reduction.
- fiat steel sheets are prepared by the electrolytic process and they are then subsequently formed into the various shapes required by the enameling industry, such forming, especially if it is accomplished with any burnishing, grinding or welding steps will either sufficiently disrupt the layer of deposited nickel or destroy it entirely so that the resultant work piece is defective because of unsatisfactory adherence in the area where these operations have been performed.
- my invention comprises the coating of the work piece with nickel which is deposited thereon from a bath wherein the nickel is generated by chemical reduction and without ion exchange between the work and bath.
- the amount of nickel deposited is critical for best results. There is one feature, however, which has an influence on the amount of nickel which will produce optimum results and that is the roughness characteristic of the steel sheet. It will be found that as the roughness or etched characteristics of the sheet vary the amount of nickel to be deposited will vary also. As indicated above, preferred results are secured when the surface preparation of the work leaves it in a deeply etched condition. On this type of surface the amount of nickel to be deposited for best results will be found to lie between about 0.04 and about 0.250 grams of nickel per sq. ft. of surface area. A coating of approximately 0.150 to 0.1750 grams of nickel per sq. ft. of surface area will generally be the preferred range.
- the baths which may be used for the chemical reduction of nickel and its deposition onto the work are described in the literature, for example U. S. Patent No. 2,532,283. These baths may be either alkaline or acid.
- the alkaline baths are described in Journal of Research- National Bureau of Standards, July 1946.
- a typical example of an alkaline bath which may be used in carrying out my invention is as follows:
- the alkaline baths have one drawback in that they are, under certain circumstances, inconvenient and uneconomical because at elevated temperatures there is a rapid loss of ammonium and the bath gives ofi copious fumes.
- the acid type baths which may be used in this step of my process are described in Journal of Research- National Bureau of Standards, November 1947.
- a representative example of an acid bath is as follows:
- Example II Nickel chloride g./liter 30 Sodium hypophosphite do 10 Sodium acetate do 10 Since the acid baths generally operate with a very low loss of constituents by vaporization this type of bath is somewhat more controllable than the alkaline type baths described above.
- hypophosphorus acid and the salts thereof may be used instead of using hypophosphorus acid and the salts thereof, the cationic portion of which is above tin in the electromotive series.
- the expression just used in the identification of the cationic portion of the salt is intended to include not only the metals, but also the ammonium radicle which can be said to have a chemical action similar to the alkali metals. While all salts formed of cations which are above tin in the electromotive series are of utility, they are by no means of equal commercial value. The alkali metals and the alkaline earth metals are very much preferred for use.
- hypophosphite salts thereof are not as active reducing agents as hypophosphorus acid and the alkali and alkaline earth and ammonium salts thereof which have been indicated as preferred. It has been found that the cadmium, zinc and chromium hypophosphites are so slow in their action that they do not lend themselves readily to continuous commercial operations where time is always a factor.
- the work is removed from the nickel bath it is washed, preferably in warm water, preparatory to receiving the application of porcelain enamel which occurs in the third step of my process.
- the application of the porcelain enamel comprises the third step of my process and should be performed within a reasonable time after the completion of the nickel deposition, in order to have a clean surface onto which to apply the porcelain enamel. It should be noted that the surface of the nickel will not change substantially from the condition in which it was, immediately after the nickel was laid down.
- the steel sheet which may be conventional cold rolled steel as produced in large quantities in this country and of appropriate gauge on the order of 18 or 20 gauge, is first cut to size and formed to the desired contour of the finished article.
- the blank thus produced is then cleaned of adhering dirt and grease by the use of a conventional alkaline cleaning bath after which the work piece is thoroughly rinsed.
- the work piece carries any rust on its surface which was not removed during the alkaline cleaning step, such rust should be removed and this can be accomplished by immersing the work piece in a sulfuric acid bath consisting of about a 6 to 7% aqueous solution of concentrated sulfuric acid, such bath being maintained at a temperature of about to F.
- the work piece is kept in this sulfuric acid for a length of time sufficient to remove the rust. Since this bath does not contain any oxidizing agent. it will not have any particular effect in producing the necessary roughened surface on the steel required as a preliminary to the application of the nickel.
- this sulfuric acid pickle step may be omitted. If it is necessary to use this sulfuric acid bath ihen the work piece, after being taken from such oath, should be thoroughly rinsed before it is subjected to the roughening step.
- the thus preliminarily cleaned work piece (which need not be dried) is then subjected to the required roughening action which can be accomplished as indicated by immersing the work in a 10% aqueous solution of nitric acid at room temperature for a period of about one minute.
- the thus roughened work piece (which need not be dried) is then immersed in any of the nickel baths referred to above under such conditions of time and temperature as to deposit thereon an amount of nickel within the limits stated.
- time and temperature conditions of this step it will be noted that when employing an acid bath as per Example II, with the bath maintained at about 70 C., the time of immersion will be on the order of about one minute to lay down the desired amount of nickel.
- the porcelain enamel used may be any of the sheet steel cover coat porcelain enamels available, a representative formula of which has been given above. As is well-known, this enamel is initially prepared in the form of a frit and a suspension thereof is then made by milling the frit in a ball mill along with suitable mill additions. The mill additions employed will depend upon the particular enamel selected for use and the other desired properties of the ultimate slip, all of which is conventional in porcelain enamelling practice.
- the enamel is applied as by dipping or spraying directly onto the nickel coated work piece and after being initially dried as is conventional in enamelling practice, is then fired under conditions which, as explained above, are the best conditions at which the particular porcelain enamel matures.
- the firing temperature as indicated will be in the neighborhood of 1400 to 1500 F. and the firing time on the order of from.
- the coated sheet which is described, was then sprayed with a cover coat enamel having an analysis substantially like that given above at a weight of about -30 grams (dry components) per sq. ft. of surface area and fired at about 1520 F. for about 3 minutes.
- the finished fired sheet had an extremely smooth texture, no surface pits or copperheads and had superior glass-metal adherence when tested by the conventional impact test used to determine adherence.
- the pickling step was performed in a 7% sulphuric acid bath containing from 1 to 3% c 3 sodium chlorate with the pickling performed at a temperature of F.
- the process comprising my invention may be used to advantage, for example, in enameling shops and when used makes possible the fabricating of the desired work pieces from untreated cold rolled steel which is one of the lowest cost forms of sheet steel available today.
- the article After the article has been completely fabricated, i. e., all welding, burnishing or like steps completed, the article is then subjected to the steps outlined and the described process will produce a finished article in which the superior surface coating is uniform throughout.
- the steps comprising immersing said roughened steel work piece in an aqueous solution of a nickel salt, said solution containing a reducing agent selected from the class consisting of hypophosphorous acid and salts thereof in which the cationic portion is above tin in the electromotive series, whereby when the steel work piece is immersed in said solution the nickel salt is reduced and nickel deposited on the work piece without ion exchange between the work piece and the solution, maintaining the work piece.
- a nickel salt selected from the class consisting of hypophosphorous acid and salts thereof in which the cationic portion is above tin in the electromotive series
- the steps comprising immersing said roughened steel work piece in an aqueous solution of a nickel salt, said solution containing as a reducing agent an alkali metal hypophosphite, whereby when the steel work piece is immersed in said solution the nickel salt is reduced and nickel deposited on the work piece without ion exchange between the work piece and the solution, maintaining the work piece in said solution until there has been deposited on the roughened surface thereof from about .04 to about .25 grams per square foot of nickel coating thereon, washing and drying the work piece, then applying directly on the thus nickelcoated roughened surface of the work piece a cover coat porcelain enamel which is substantially free of adherence promoting oxides, and then firing such enamel thereon.
- the steps comprising immersing said roughened steel work piece in an aqueous solution of a nickel salt, said solution containing as a reducing agent an alkaline earth metal hypophosphite, whereby when the steel work piece is immersed in said solution the nickel salt is reduced and nickel deposited on the work-piece without ion exchange between the work piece and the solution, maintaining the work piece in said solution until there has been deposited on the roughened surface thereof from about .04 to about .25 grams per square foot of nickel coating thereon, washing and drying the work piece, then applying directly on the thus nickel-coated roughened surface of the work piece a cover coat porcelain enamel which is substantially free of adherence promoting oxides, and then firing such enamel thereon.
- the steps comprising immersing said roughened steel work piece in an aqueous solution of a nickel salt, said solution containing as a reducing agent hypophosphorous acid, whereby when the steel work piece is immersed in said solution the nickel salt is reduced and nickel deposited on the work piece without ion exchange between the work piece and the solution, maintaining the work piece in said solution until there has been deposited on the roughened surface thereof from about .04 to about .25 grams per square foot of nickel coating thereon, washing and drying the work piece, then applying directly on the thus nickel-coated roughened surface of the work piece a cover coat porcelain enamel which is substantially free of adherence promoting oxides, and then firing such enamel thereon.
- the method of porcelain enamelling a steel work piece which comprises cleaning and roughening the surface of the work piece so as to produce deep sharp edged pits therein by means of an aqueous solution of nitric acid, immersing said roughened steel work piece in an aqueous solution of a nickel salt, said solution containing as a reducing agent sodium hypophosphite, whereby when the steel work piece is immersed in said solution the nickel salt is reduced and nickel deposited on the work piece without ion exchange between the work piece and the solution, maintaining the work piece in said solution until there has been deposited on the roughened surface thereof from about .04 to about .25 grams per square foot of nickel coating thereon, washing and drying the work piece, then applying directly on the thus nickel-coated roughened surface of the work piece a cover coat porcelain enamel which is substantially free of adherence promoting oxides, and then firing such enamel thereon.
Description
Patented Jan. I, 1952 PORCELAIN ENAMEL ARTICLE AND METHOD OF PRODUCING SAME Benjamin J. Sweo, Lakewood, Ohio, aasignor to Fem Corporation, Cleveland, Ohio, a corporation of Ohio No Drawing. Application November 6, 1951, Serial No. 255,130
8 Claims. (Cl. 111-53) The present invention is a continuation-111+ part of my co-pending invention bearing Serial Number 139,963 filed January 21, 1950, entitled Porcelain Enamel Article and Method of Producing Same, now abandoned.
This invention relates, as indicated, to per.- celain enameling and has more particular reference to an enameling procedure and articles produced therefrom characterized by the direct application to a steel surface of porcelain enamel of the type ordinarily referred to. as cover coat porcelain enamel in that it does not contain any substantial amounts of those materials, such as oxides of cobalt and nickel for example, which have heretofore been deemed necessary in order to insure satisfactory adherence between the enamel and the steel.
As indicated above, the prior art practice of insuring adequate adherence between enamel and steel has been to use adherence-promoting oxides. These are, however, usually dark in color so that if the finished product is to be white,
or of a light shade it has been necessary to.
apphf a cover coat of such light enamel. Various methods have been used in an endeavor to improve the adherence of cover coat enamels to steel. One of such methods has been by the use of steels of special compositions. Another has been by the use of a so-called nickel flash" step by which a predetermined amount of nickel is deposited on the surface by galvanic action. The use of special steels is undesirable for many reasons, the principal one being cost.
The use of the galvanic process for the deposition of nickel onto the steel surface to promote adherence between the enamel and the steel has been only partially successful. By the use of the nickel flash" method the adherence of the enamel to the steel has been improved. However, that method leads to inconsistent results in that the nickel deposits on various steels from a conventional bath varies in character and amount. Thus while the nickel flash" formation method has been used for the purposes of improving the bond between the enamel and the steel, that improvement has never been great enough to make possible the omission from the enamels of at least certain amounts of adherence-promoting oxides so that in most cases the industry has continued to use the twocoat process when producing light colored work, a first or ground coat-of dark colored enamel and a second coat of the desired light color.
It is the principal object of my invention to provide a porcelain enameled article and a meth- 0d of producing the same characterized by the direct application to the work piece of enamels which do not require the use of a ground coat or the presence therein of any substantial amounts of adherence-promoting oxides and the like.
It is a further object of my invention to provide porcelain enameled. articles which are superior from the standpoint of surface characteristics and appearance with respect to any which have beenbapable of production by any known prior art methods. Other objects of my invention will appear as the description proceeds.
To the accomplishment of the foregoing and related ends, said invention then comprises the features hereinafter fully described and particularly pointed out in the claims, the following description setting forth in detail certain illustrative embodiments of the invention, these being indicative, however, of but a few of the various ways in which the principle of the invention may be employed.
Broadly stated, this invention comprises the method of porcelain enamelling a steel work piece which comprises cleaning and roughening the surface of the work piece so as to produce a surface condition characterized by deep sharp edged pits therein characteristic of the surface resulting from pickling with an aqueous solution of nitric acid, immersing said roughened steel work piece in an aqueous solution of a nickel salt, said solution containing a. reducing agent selected from the class consisting of hypophosphorous acid and those salts thereof, the cationic portion of which is above tin in the electromotive series whereby when the steel work piece is immersed in said solution the nickel salt is reduced and nickel deposited on the work piece without ion exchange between the work piece and the solution, maintaining the work piece in said solution until there has been deposited on the roughened surface thereof from about .04 to about .25 grams per square foot of nickel coating thereon, washing and drying the work piece, then applying directly on the thus nickelcoated roughened surface of the work piece a cover coat porcelain enamel which is substantially free of adherence promoting oxides, and then firing such enamel thereon.
It will be observed from the foregoing broad statement of my invention that the method which comprises such invention for the production of articles which are likewise new, in that they have never been made heretofore, may be divided into three principal steps which for convenience in the further description of my invention will be treated in the order in which they are usually performed.
CLEANING AND ROUGEENING THE METAL The steel surface to which the porcelain enamel is to be eventually applied when practicing my invention needs to have two primary characteristics. First, it must be relatively clean, that is free from all foreign materials such as dirt, grease and the usual coat of metallic oxide. Second the surface of the steel must be reasonably rough for best adherence of the porcelain enamel. This preparation of the steel surface may be accomplished by chemical means or by mechanical means or by a combination of the two. If it is desirable to effect the preparation of the surface by chemical means only, this can be accomplished conveniently by the use of pickling baths which leave a relatively rough surface. The pickling baths which are available for this purposes are, for example those employing nitric acid and combinations of nitric acid with other acids and baths which are primarily sulphuric acid baths, but which also contain nitric acid or other oxidizing agents. This type of bath has two principal characteristics. First the bath is extremely vigorous in its action so that the required pickling time is relatively short and second, this type of bath produces a surface which may be identified, for convenience, as a deeply etched surface, in that it contains pits which are relatively deep with the crests between such pits relatively sharp. Because of this peculiar type of surface just described which is produced by pickling baths of the type ust described they are preferred for use in my process since it has been found that adherence between the enamel and the steel is greatest when the steel surface is thus preliminarily prepared.
Instead of utilizing baths of the character referred to above satisfactory results may be obtained by utilizing pickling baths in which the principal components are salts which are readily reduced in the presence of iron, for example, trivalent iron salts such as ferric chloride. Since the ferric chloride pickling process wherein the effective components of the bath are continuously regenerated by the introduction of chlorine thereto are well-known in the pickling art, it is believed unnecessary to further describe such process at this point.
All of the various pickling processes referred to above are capable of producing; the roughened surface on the work which is characterized by deep sharp-edged pits therein. This type of surface preferably is produced by means of a pickling solution which is an aqueous solution of nitric acid containing about one part of concentrated nitric acid to each four parts oi; water. When using such a bath, a satisfactory surface will usually be produced in about one minute at room temperature. As the temperature increases the time is accordinghr reduced. Typical examples of sulphuric acid baths containing oxidizing agents which are effective to produce a surface characterized by deep sharp-edged pits therein The length of time during which the work piece must be immersed in baths of the type represented by the last two examples above will depend not only on the temperature of the bath, but also on the relative concentrations of sulfuric acid and oxldizng agent. The sodium chlorate bath given above will usually produce a satisfactory surface, when operated at 160 F. temperature, for 3 minutes. The sulfuric acid bath utilizing nitric acid as the oxidizing agent as given above when operated at F. temperature will produce a satisfactory result in about 3 minutes.
Instead of chemically preparing the surface of the steel in the manner just described satisfactory results may be secured by a. simple sand blasting operation which is effective to not only remove the foreign material and oxides from the sheet, but also leave the sheet reasonably rough for the reception of the nickel deposit. It is within the contemplation of my invention to combine chemical and physical means for the preparation of the sheet and in this the sand blasting operation which is described may be preceded or followed by a second step and when the pickling step is the last to be employed then it should preferably be of the type which will produce the deeply etched surface of the character previously described.
NICKEL DEPOSITIONS The nickel flash method previously referred to, i. e. the process for the deposition of nickel which depends upon galvanic action by the work piece and the bath has not been satisfactory for use in my process. It is believed that one reason why deposition of the nickel by galvanic action does not give satisfactory results is not only the inconsistency of that process and the variations in the deposits resulting therefrom, but also the nature of character of the nickel deposit resulting from such process. Since the very nature of the process is galvani this requires that there be a certain area of the steel surface always exposed to the action of the bath if the galvanic process is to proceed. The nickel layer thus laid down by the galvanic process is not what may be termed a uniform or substantially continuous layer of nickel. Instead it is a coating of nickel which is interrupted by areas wherein the base metal is exposed or only superficially coated.
It has been established that porcelain enamel deposited over a thick layer of pure nickel has very poor adherence to such nickel. It will be concluded therefore that for proper adherence by the enamel to the work piece there must be a certain amount of iron in combination or elemental form available in the bonded area. I have found that the iron thus available on a surface coated with nickel by the galvanic method is too great for best results and it is believed that this accounts for the poor bond which is secured between the base metal and the enamel if only galvanically deposited nickel is used and if there are no adherence-promoting oxides present in the porcelain enamel.
In order to provide a lower ratio of iron to nickel on the surface of the steel work piece and to bring such ratio into the range wherein greatest adherence between the enamel and the work piece is secured, it is essential that the nickel coating deposit be substantially uniform while at the same time permitting the occurrence of at least a minor amount of iron, in' free or combined form, at the bond. The process of depositing nickel by means of an electrolytic bath will produce a substantially continuous layer of nickel but such process is unsatisfactory for a number of reasons. First it can be used successfully only on simple shapes suchas flat sheets because if the article treated has any substantial contour deviating from a fiat plane there will be sufficient variation in the thickness of the nickel deposited on the various areas of the article to produce best results. Since the nature of the nickel deposit, 1. e. its thickness and character are quite critical, when the article is contoured the thickness of the coat on the high points, for example, will be sufllciently different from the thickness of the coat on the low points for example, so that if the coating at one place is adjusted to the narrower range for best results, the coating on the other area will be outside of such range. Thus the process of depositing the nickel electrolytically can be used satisfactorily only on flat surfaces such as unfabricated steel sheets and strips and even on such surfaces the character of the deposit laid down by the electrolytic method is sufliciently different from the character of the deposits laid down by a chemical reduction method that it is not possible to secure the high order of adherence with the electrolytic process as it is with the process wherein the nickel is laid down by chemical reduction. When fiat steel sheets are prepared by the electrolytic process and they are then subsequently formed into the various shapes required by the enameling industry, such forming, especially if it is accomplished with any burnishing, grinding or welding steps will either sufficiently disrupt the layer of deposited nickel or destroy it entirely so that the resultant work piece is defective because of unsatisfactory adherence in the area where these operations have been performed.
Accordingly my invention comprises the coating of the work piece with nickel which is deposited thereon from a bath wherein the nickel is generated by chemical reduction and without ion exchange between the work and bath.
As previously indicated, the amount of nickel deposited is critical for best results. There is one feature, however, which has an influence on the amount of nickel which will produce optimum results and that is the roughness characteristic of the steel sheet. It will be found that as the roughness or etched characteristics of the sheet vary the amount of nickel to be deposited will vary also. As indicated above, preferred results are secured when the surface preparation of the work leaves it in a deeply etched condition. On this type of surface the amount of nickel to be deposited for best results will be found to lie between about 0.04 and about 0.250 grams of nickel per sq. ft. of surface area. A coating of approximately 0.150 to 0.1750 grams of nickel per sq. ft. of surface area will generally be the preferred range. The baths which may be used for the chemical reduction of nickel and its deposition onto the work are described in the literature, for example U. S. Patent No. 2,532,283. These baths may be either alkaline or acid. The alkaline baths are described in Journal of Research- National Bureau of Standards, July 1946. A typical example of an alkaline bath which may be used in carrying out my invention is as follows:
ExampleI Nickel chloride g./liter Sodium hypophosphite do 10 Ammonium chloride .do.. Sodium citrate do 100 Ammonium hydroxide to a pH of 8 to 10 The alkaline baths have one drawback in that they are, under certain circumstances, inconvenient and uneconomical because at elevated temperatures there is a rapid loss of ammonium and the bath gives ofi copious fumes. The acid type baths which may be used in this step of my process are described in Journal of Research- National Bureau of Standards, November 1947. A representative example of an acid bath is as follows:
Example II Nickel chloride g./liter 30 Sodium hypophosphite do 10 Sodium acetate do 10 Since the acid baths generally operate with a very low loss of constituents by vaporization this type of bath is somewhat more controllable than the alkaline type baths described above.
While the aforegoing examples of plating baths show the use of sodium hypophosphite as the reducing agent I have successfully used various other hypophosphite salts and hypophosphorus acid, however, since the sodium salt is the cheapest and most readily obtainable I prefer the use of sodium hypophosphite.
Instead of employing sodium hypophosphite as the reducing agent in the nickel plating baths I may use instead hypophosphorus acid and the salts thereof, the cationic portion of which is above tin in the electromotive series. The expression just used in the identification of the cationic portion of the salt is intended to include not only the metals, but also the ammonium radicle which can be said to have a chemical action similar to the alkali metals. While all salts formed of cations which are above tin in the electromotive series are of utility, they are by no means of equal commercial value. The alkali metals and the alkaline earth metals are very much preferred for use. While cadmium, zinc and chromium occur in the electromotive series above tin and are useful, the hypophosphite salts thereof are not as active reducing agents as hypophosphorus acid and the alkali and alkaline earth and ammonium salts thereof which have been indicated as preferred. It has been found that the cadmium, zinc and chromium hypophosphites are so slow in their action that they do not lend themselves readily to continuous commercial operations where time is always a factor.
The following is a list of examples of additional nickel plating baths employing hypophosphites other than the preferred sodium hypophosphite used in examples I and 11.
7 Example VI Nickel chloride -g./liter 30 Magnesium hypophosphite do 24.6 Sodium acetate do pH 4 to 6 Example VII Nickel chloride g./liter 80 HypOphosphorus acid (30%) .ml./liter 17.8 Sodium acetate g./liter 10 pH 4 to 6 Example VIII Nickel chloride g./liter 30 Manganous hypophosphite do 9.6 Sodium acetate do 10 pH 4 to 6 Example IX Nickel chloride g./liter 30 Ferrous hypophosphite do 8.8 Sodium acetate do 10 pH 4 to 6 Example X Nickel chloride g./liter 30 Aluminum hypophosphite do 7 Sodium acetate do 10 pH 4 to 6 Example XI Nickel chloride g./liter 30 Nickel hypophosphite do 14 Sodium acetate do 10 pH 4 to 6 Example XII Nickel chloride g./iiter 30 Cobalt hypophosphite do 8.9 Sodium acetate do 10 pH 4 to 6 Example XIII Nickel chloride g./liter- 30 Zinc hypophosphite do 92 Sodium acetate do 10 pH 4 to 6 In carrying out the nickel deposition step the previously treated sheet as prepared by step 1 of my improved process is immersed in the bath for a length of time on the order to about one minute at about 70 0., i. e., for a period of time dependin on temperature and other conditions such as the condition of the bath in order to lay down a deposit of nickel within the ranges specified above. After the work is removed from the nickel bath it is washed, preferably in warm water, preparatory to receiving the application of porcelain enamel which occurs in the third step of my process. The application of the porcelain enamel comprises the third step of my process and should be performed within a reasonable time after the completion of the nickel deposition, in order to have a clean surface onto which to apply the porcelain enamel. It should be noted that the surface of the nickel will not change substantially from the condition in which it was, immediately after the nickel was laid down.
THE ENAMEL STEP This third step of my process is substantially conventional porcelain enameling practice such as would be followed in the application of cover coats to work pieces previously provided with Dehydrated Borax ..-.Jbs.-.. 159 Feldspar do 143 Sodium nitrate do.. 364 Cryolite do" 195 Zinc oxide do 96 Boric acid do 345 Powdered quartz do 1204 Titanium dioxide do 294 The foregoing enamel fires out on 20 gauge steel in about 3% minutes at about 1480 F. It will be found that when carrying out my process and utilizing conventional sheet steel cover coat porcelain enamels, of which there are many variations available, best results will be secured if the porcelain enamel is fired slightly harder than the conditions under which it would be fired as applied over a ground coat. Thus, the porcelain enamel given above which would normally be fired over a ground coat for 3% minutes at 1480" F. gives unexpected superior results when fired out at about 1520 F. for the same length of time.
The following is a representative series of steps which may be followed in the process of producing a porcelain enamelled sheet steel article when utilizing my invention.
The steel sheet, which may be conventional cold rolled steel as produced in large quantities in this country and of appropriate gauge on the order of 18 or 20 gauge, is first cut to size and formed to the desired contour of the finished article. The blank thus produced is then cleaned of adhering dirt and grease by the use of a conventional alkaline cleaning bath after which the work piece is thoroughly rinsed.
If the work piece carries any rust on its surface which was not removed during the alkaline cleaning step, such rust should be removed and this can be accomplished by immersing the work piece in a sulfuric acid bath consisting of about a 6 to 7% aqueous solution of concentrated sulfuric acid, such bath being maintained at a temperature of about to F. The work piece is kept in this sulfuric acid for a length of time sufficient to remove the rust. Since this bath does not contain any oxidizing agent. it will not have any particular effect in producing the necessary roughened surface on the steel required as a preliminary to the application of the nickel. If the work piece does not carry any rust, this sulfuric acid pickle step may be omitted. If it is necessary to use this sulfuric acid bath ihen the work piece, after being taken from such oath, should be thoroughly rinsed before it is subjected to the roughening step.
The thus preliminarily cleaned work piece (which need not be dried) is then subjected to the required roughening action which can be accomplished as indicated by immersing the work in a 10% aqueous solution of nitric acid at room temperature for a period of about one minute.
After the work is removed from the nitric acid bath it should be washed with water and then immediately dipped several times in a 6 to 7% aqueous solution of concentrated sulfuric acid at a temperature of about 140 to 150 F. to remove from the surface any salts which may have been formed thereon by the reaction of the nitric acid with the work. The work is then again washed with water.
The thus roughened work piece (which need not be dried) is then immersed in any of the nickel baths referred to above under such conditions of time and temperature as to deposit thereon an amount of nickel within the limits stated. As an indication of the time and temperature conditions of this step it will be noted that when employing an acid bath as per Example II, with the bath maintained at about 70 C., the time of immersion will be on the order of about one minute to lay down the desired amount of nickel.
After the work is removed from the nickel plating bath it is then washed again and preferably dried before the application of the porcelain enamel thereto.
The porcelain enamel used may be any of the sheet steel cover coat porcelain enamels available, a representative formula of which has been given above. As is well-known, this enamel is initially prepared in the form of a frit and a suspension thereof is then made by milling the frit in a ball mill along with suitable mill additions. The mill additions employed will depend upon the particular enamel selected for use and the other desired properties of the ultimate slip, all of which is conventional in porcelain enamelling practice.
The enamel is applied as by dipping or spraying directly onto the nickel coated work piece and after being initially dried as is conventional in enamelling practice, is then fired under conditions which, as explained above, are the best conditions at which the particular porcelain enamel matures. The firing temperature as indicated will be in the neighborhood of 1400 to 1500 F. and the firing time on the order of from.
2 to minutes.
As a striking example of the unexpected results which can be secured by the use of my process, a sample of ordinary cold rolled steel. which up to the time of my invention was considered to be practically unusable for direct cover coat application, was pickled at room temperature in a nitric acid bath comprising one volume of nitric acid to four volumes of water; pickling time one minute. The sheet was then rinsed in warm water and immersed in the chemical acid reduction nickel bath, the analysis of which has been given above, at a temperature of 70 C. for one minute. The sheet was then rinsed again in warm water and dried. By chemical analysis the sheet was found to carry a coating of .163 grams of nickel per sq. ft. of surface area.
The coated sheet, which is described, was then sprayed with a cover coat enamel having an analysis substantially like that given above at a weight of about -30 grams (dry components) per sq. ft. of surface area and fired at about 1520 F. for about 3 minutes. The finished fired sheet had an extremely smooth texture, no surface pits or copperheads and had superior glass-metal adherence when tested by the conventional impact test used to determine adherence. In another test on the same base equally satisfactory results were re-cured by the same procedure excepting that the pickling step was performed in a 7% sulphuric acid bath containing from 1 to 3% c 3 sodium chlorate with the pickling performed at a temperature of F. The process comprising my invention may be used to advantage, for example, in enameling shops and when used makes possible the fabricating of the desired work pieces from untreated cold rolled steel which is one of the lowest cost forms of sheet steel available today. After the article has been completely fabricated, i. e., all welding, burnishing or like steps completed, the article is then subjected to the steps outlined and the described process will produce a finished article in which the superior surface coating is uniform throughout.
Other modes of applying the principle of the invention may be employed, change being made as regards the details described, provided the features stated in any of the following claims or the equivalent of such be employed.
I therefore particularly point out and distinctly claim as my invention:
1. In the method of porcelain enamelling a cleaned and roughened steel work piece surface having deep sharp edged pits therein, the steps comprising immersing said roughened steel work piece in an aqueous solution of a nickel salt, said solution containing a reducing agent selected from the class consisting of hypophosphorous acid and salts thereof in which the cationic portion is above tin in the electromotive series, whereby when the steel work piece is immersed in said solution the nickel salt is reduced and nickel deposited on the work piece without ion exchange between the work piece and the solution, maintaining the work piece. in said solution until there has been deposited on the roughened surface thereof from about .04 to about .25 grams per square foot of nickel coating thereon, washing and drying the work piece, then applying directly on the thus nickel-coated roughened surface of the work piece a cover coat porcelain enamel which is substantially free of adherence promoting oxides. and then firing such enamel thereon. I
2. In the method of porcelain enamelling a cleaned and roughened steel work piece surface having deep sharp edged pits therein, the steps comprising immersing said roughened steel work piece in an aqueous solution of a nickel salt, said solution containing as a reducing agent an alkali metal hypophosphite, whereby when the steel work piece is immersed in said solution the nickel salt is reduced and nickel deposited on the work piece without ion exchange between the work piece and the solution, maintaining the work piece in said solution until there has been deposited on the roughened surface thereof from about .04 to about .25 grams per square foot of nickel coating thereon, washing and drying the work piece, then applying directly on the thus nickelcoated roughened surface of the work piece a cover coat porcelain enamel which is substantially free of adherence promoting oxides, and then firing such enamel thereon.
3. In the method of porcelain enamelling a cleaned and roughened steel work piece surface having deep sharp edged pits therein, the steps comprising immersing said roughened steel work piece in an aqueous solution of a nickel salt, said solution containing as a reducing agent an alkaline earth metal hypophosphite, whereby when the steel work piece is immersed in said solution the nickel salt is reduced and nickel deposited on the work-piece without ion exchange between the work piece and the solution, maintaining the work piece in said solution until there has been deposited on the roughened surface thereof from about .04 to about .25 grams per square foot of nickel coating thereon, washing and drying the work piece, then applying directly on the thus nickel-coated roughened surface of the work piece a cover coat porcelain enamel which is substantially free of adherence promoting oxides, and then firing such enamel thereon.
4. In the method of porcelain enamelling a cleaned and roughened steel work piece surface having deep sharp edged pits therein, the steps comprising immersing said roughened steel work piece in an aqueous solution of a nickel salt, said solution containing as a reducing agent hypophosphorous acid, whereby when the steel work piece is immersed in said solution the nickel salt is reduced and nickel deposited on the work piece without ion exchange between the work piece and the solution, maintaining the work piece in said solution until there has been deposited on the roughened surface thereof from about .04 to about .25 grams per square foot of nickel coating thereon, washing and drying the work piece, then applying directly on the thus nickel-coated roughened surface of the work piece a cover coat porcelain enamel which is substantially free of adherence promoting oxides, and then firing such enamel thereon.
5. The method of porcelain enamelling a steel work piecewhich comprises cleaning and roughening the surface of the work piece so as to produce deep sharp edged pits therein by means of an aqueous solution of nitric acid, immersing said roughened steel work piece in an aqueous solution of a nickel salt, said solution containing as a reducing agent sodium hypophosphite, whereby when the steel work piece is immersed in said solution the nickel salt is reduced and nickel deposited on the work piece without ion exchange between the work piece and the solution, maintaining the work piece in said solution until there has been deposited on the roughened surface thereof from about .04 to about .25 grams per square foot of nickel coating thereon, washing and drying the work piece, then applying directly on the thus nickel-coated roughened surface of the work piece a cover coat porcelain enamel which is substantially free of adherence promoting oxides, and then firing such enamel thereon.
6. As a new article of manufacture, a porcelain enamelied steel article produced by the process of claim 1.
BENJAMIN J. SWEO.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,032,256 Canfleld Feb. 25, 1936 2,101,950 McGohan Dec. 14, 1937 2,109,487 Kreidl Mar. 1, 1938 2,265,467 Alexander Dec. 9, 1941 2,532,283 Brenner et al. Dec. 5. i950
Claims (2)
1. IN THE METHOD OF PROCELAIN ENAMELLING A CLEANED AND ROUGHENED STEEL WORK PIECE SURFACE HAVING DEEP SHARP EDGED PITS THEREIN, THE STEPS COMPRISING IMMERSING SAID ROUGHENED STEEL WORK PIECE IN AN AQUEOUS SOLUTION OF A NICKEL SALT, SAID SOLUTION CONTAINING A REDUCING AGENT SELECTED FROM THE CLASS CONSISTING OF HYPOPHOSPHOROUS ACID AND SALTS THEREOF IN WHICH THE CATIONIC PORTION IS ABOVE TIN IN THE ELECTROMOTIVE SERIES, WHEREBY WHEN THE STEEL WORK PIECE IS IMMERSED IN SAID SOLUTION THE NICKEL SALT IS REDUCED AND NICKEL DEPOSITED ON THE WORK PIECE WITHOUT ION EXCHANGE BETWEEN THE WORK PIECE AND THE SOLUTION, MAINTAINING THE WORK PIECE IN SAID SOLUTION UNTIL THERE HAS BEEN DEPOSITED ON THE ROUGHENED SURFACE THEREOF FROM ABOUT .04 TO ABOUT .25 GRAMS PER SQUARE FOOT OF NICKEL COATING THEREON, WASHING AND DRYING THE WORK PIECE, THEN APPLYING DIRECTLY ON THE THUS NICKEL-COATED ROUGHENED SURFACE OF THE WORK PIECE A COVER COAT PORCELAIN ENAMEL WHICH IS SUBSTANTIALLY FREE OF ADHERENCE PROMOTING OXIDES, AND THEN FIRING SUCH ENAMEL THEREON.
6. AS A NEW ARTICLE OF MANUFACTURE, A PORCELAIN ENAMELLED STEEL ARTICLE PRODUCED BY THE PROCESS OF CLAIM 1.
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
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BE508136D BE508136A (en) | 1950-01-21 | ||
GB16032/50A GB680844A (en) | 1950-01-21 | 1950-06-27 | Improvement in porcelain enamel article and method of producing same |
US255130A US2581310A (en) | 1951-11-06 | 1951-11-06 | Porcelain enamel article and method of producing same |
FR1054289D FR1054289A (en) | 1950-01-21 | 1951-12-27 | Porcelain enamel article and its manufacturing process |
GB30362/51A GB706450A (en) | 1950-01-21 | 1951-12-28 | Improvements in or relating to the porcelain enamelling of steel articles |
CH309198D CH309198A (en) | 1950-01-21 | 1951-12-29 | Enamelling process of a steel part and enamelled part obtained by this process. |
DEF8047A DE913977C (en) | 1950-01-21 | 1952-01-01 | Enamelling process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US255130A US2581310A (en) | 1951-11-06 | 1951-11-06 | Porcelain enamel article and method of producing same |
Publications (1)
Publication Number | Publication Date |
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US2581310A true US2581310A (en) | 1952-01-01 |
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Application Number | Title | Priority Date | Filing Date |
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US255130A Expired - Lifetime US2581310A (en) | 1950-01-21 | 1951-11-06 | Porcelain enamel article and method of producing same |
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Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2609594A (en) * | 1949-10-18 | 1952-09-09 | Gilron Products Company | Method of producing vitreous enamelled metal articles |
US2695249A (en) * | 1950-04-05 | 1954-11-23 | Ferro Corp | Porcelain enamel article and method of making same |
US2772183A (en) * | 1953-09-24 | 1956-11-27 | Gen Am Transport | Chemical nickel plating processes |
US2872352A (en) * | 1953-06-11 | 1959-02-03 | Inland Steel Co | Method of producing articles for enamelling |
US2886498A (en) * | 1957-09-06 | 1959-05-12 | Republic Steel Corp | Process of preparing steel for enameling |
US2908419A (en) * | 1955-06-10 | 1959-10-13 | Gen Am Transport | Lined containers and methods of making the same |
US2940865A (en) * | 1957-10-14 | 1960-06-14 | Smith Corp A O | Method of applying a glass coating to steel by using an intermediate layer of nickelous oxide |
US2961337A (en) * | 1958-10-08 | 1960-11-22 | Ferro Corp | Method of metal preparation for porcelain enameling |
US2975072A (en) * | 1958-12-09 | 1961-03-14 | Ferro Corp | Protective coatings for combustion engine exhaust systems |
US2976171A (en) * | 1957-10-14 | 1961-03-21 | Smith Corp A O | Glass coated steel structure and method of making the same |
US3378400A (en) * | 1965-07-30 | 1968-04-16 | Ralph E. Sickles | Autocatalytic deposition of nickel, cobalt and alloys thereof |
NL6915235A (en) * | 1968-10-10 | 1970-04-14 | ||
US4861625A (en) * | 1984-12-27 | 1989-08-29 | Ngb Spark Plug Co., Ltd. | Method of manufacturing a thermal printing head having a partially-glazed ceramic substrate |
US5920977A (en) * | 1995-12-07 | 1999-07-13 | Wyckoff; James L. | Porcelain coated substrate and process for making same |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2032256A (en) * | 1932-09-06 | 1936-02-25 | American Rolling Mill Co | Metal articles for coating |
US2101950A (en) * | 1934-03-21 | 1937-12-14 | American Rolling Mill Co | Preparing metal for enameling |
US2109487A (en) * | 1931-02-12 | 1938-03-01 | Kreidl Ignaz | Enameled ware |
US2265467A (en) * | 1939-02-23 | 1941-12-09 | Gen Motors Corp | Control of nickel-dip solutions |
US2532283A (en) * | 1947-05-05 | 1950-12-05 | Brenner Abner | Nickel plating by chemical reduction |
-
1951
- 1951-11-06 US US255130A patent/US2581310A/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2109487A (en) * | 1931-02-12 | 1938-03-01 | Kreidl Ignaz | Enameled ware |
US2032256A (en) * | 1932-09-06 | 1936-02-25 | American Rolling Mill Co | Metal articles for coating |
US2101950A (en) * | 1934-03-21 | 1937-12-14 | American Rolling Mill Co | Preparing metal for enameling |
US2265467A (en) * | 1939-02-23 | 1941-12-09 | Gen Motors Corp | Control of nickel-dip solutions |
US2532283A (en) * | 1947-05-05 | 1950-12-05 | Brenner Abner | Nickel plating by chemical reduction |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2609594A (en) * | 1949-10-18 | 1952-09-09 | Gilron Products Company | Method of producing vitreous enamelled metal articles |
US2695249A (en) * | 1950-04-05 | 1954-11-23 | Ferro Corp | Porcelain enamel article and method of making same |
US2872352A (en) * | 1953-06-11 | 1959-02-03 | Inland Steel Co | Method of producing articles for enamelling |
US2772183A (en) * | 1953-09-24 | 1956-11-27 | Gen Am Transport | Chemical nickel plating processes |
US2908419A (en) * | 1955-06-10 | 1959-10-13 | Gen Am Transport | Lined containers and methods of making the same |
US2886498A (en) * | 1957-09-06 | 1959-05-12 | Republic Steel Corp | Process of preparing steel for enameling |
US2940865A (en) * | 1957-10-14 | 1960-06-14 | Smith Corp A O | Method of applying a glass coating to steel by using an intermediate layer of nickelous oxide |
US2976171A (en) * | 1957-10-14 | 1961-03-21 | Smith Corp A O | Glass coated steel structure and method of making the same |
US2961337A (en) * | 1958-10-08 | 1960-11-22 | Ferro Corp | Method of metal preparation for porcelain enameling |
US2975072A (en) * | 1958-12-09 | 1961-03-14 | Ferro Corp | Protective coatings for combustion engine exhaust systems |
US3378400A (en) * | 1965-07-30 | 1968-04-16 | Ralph E. Sickles | Autocatalytic deposition of nickel, cobalt and alloys thereof |
NL6915235A (en) * | 1968-10-10 | 1970-04-14 | ||
US4861625A (en) * | 1984-12-27 | 1989-08-29 | Ngb Spark Plug Co., Ltd. | Method of manufacturing a thermal printing head having a partially-glazed ceramic substrate |
US5920977A (en) * | 1995-12-07 | 1999-07-13 | Wyckoff; James L. | Porcelain coated substrate and process for making same |
US6233857B1 (en) | 1995-12-07 | 2001-05-22 | Photo-Cut Graphics, Inc. | Porcelain coated substrate and process for making same |
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