US2462197A - Etching method - Google Patents
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- US2462197A US2462197A US555979A US55597944A US2462197A US 2462197 A US2462197 A US 2462197A US 555979 A US555979 A US 555979A US 55597944 A US55597944 A US 55597944A US 2462197 A US2462197 A US 2462197A
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- copper
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25F—PROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
- C25F3/00—Electrolytic etching or polishing
- C25F3/02—Etching
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- the object of this invention is to provide for treating metal surfaces to produce a surface .structure for better adhesion of Aorganic nishes. ⁇ Other objects of the invention will in part be obvious and will inpart appear hereinafter.
- Figure 1 is a schematic elevational view of an apparatus for carrying out the invention
- Fig. 2 is a fragmentarysectional view showing a metal sheet provided with an organic finish
- Fig. 3 i-s a photomicrograph of the surface of a sheetof brass treated according to the invention.
- Fig. 4 is a photomicrograph of the surface -of la. sheet of untreated cold rolled brass.
- thel finish will either .crack and flake :off .orelse lose its adhesion to the copper base sheet and ,upon b eingfsubjected to slight mechanical :abrasion willqeasily beremoved.
- the failureof the organicinsh is undesirable. Accordingly the manutaetureris frequently forced to substitute'metals which are more expensive than copper base alloys paramount to avoid this objectionable feature.
- copper :base ,alloys in the form of sheets, machined parts, vforgings and other smooth surfaced shapes are subjected to an'electrolytic treatment Wherebi7 ,the surface of the metal is given a tooth ormicroscopic roughening suiicient f or a greatly enhanced ad.
- the metal When provided with such a surface, the metal may be bent and subjected to ,other stresses without premature failure of the coating of Vorganic finish by flaking and the like. Furthermore, the organic iinishpnplectrclytically treated surfaces vwill withstand considerably more abrasion before lossof the organic vfinish than on untreated surfaces.
- This treatment Willproduce a suiiicient microscopic alteration ,of the metal to rougher; and pit the surface vto provide a ⁇ greatly improved adherence .of organic ⁇ finishes. togthe surface.
- the apparatus ⁇ ll f .for carrying out the etohingpperation includes an endless conveyor tracky l2 whereby-copper Vbase members to ⁇ be electrolytically etchedaare carried through the entire process of operations.
- VAt portion .1li .of the conveyor I2 is lccatedf a loading statio-nfor loading articles 38 iiponcon veyors zfonsubsequent processing.'
- The'gmembers 38 are suspended upon hooks 3,2 of the conveyor 28 provided'with Wheel-S30 for-travelalong track l2.
- the etching solution tank 48 is made the cathode by connecting thereto a direct current cathode conductor 44 to a portion of the tank 48.
- the tank 40 is made of some conducting metal which will be resistant Ito the etching solution.
- a lead liner, for example, is satisfactory for the purpose, but steel cathode liners are preferred.
- the etching solution 42 is an equeous electrolyte containing from 20% to 85% phosphoric acid (H3PO4) by weight from 0.1% to 25% nitric acid by weight.
- the solutions with higher concentrations of phosphoric acid are employed for copper base metals which contain the higher percentages of copper.
- the main function of the nitric acidin the electrolytic solution appears to be to remove a surface layer of soft non-adherent copper parfticles which form during'the electrolytic treatment.
- the electrolyte of phosphoric acid and nitric acid operates satisfactorily when applied to copper base alloys having substantially no impurities, particularly metallic impurities such as lead, arsenic, and iron. If these metallic impurities are present in the copper base alloy, 'a surface smut may be left on the electro-etched copper alloy. It has been found that the additionof oxidizing compounds of chromium and oxygen, such for example, as chromic acid, sodium chromate and potassium dichromate, to the electrolyte will prevent formation of the smut. The amount of the chromium and oxygen compound may be as much as of the weight of the bath.
- the electrolyte solution was prepared from 1450 milliliters of 85% Hal-O4 and 150 milliliters of 70% HNOa diluted with Water -to Ia roughly 45% by weight phosphoric acidand 3% by weight nitric acid,
- the solution containedbrass for example, a solution having 50% phos-4 phoric acid, 1% nitricacid and 1/2% potassium dichromate by weight gave a highly effective etch in four minutes at a current density of 40 amperes per square foot.
- the proportions of the electrolyte composition obviously may bermodifled for different amounts and kinds of impurities and the copper base alloys being subjected to the treatment.
- the copper base alloy metal After the copper base alloy metal has been electrolytically etched, washed and dried, an examination of the surface will reveal a marked dulling of the original bright finish due mainly to the fact that the surface has Ibeen preferentially etched to produce a roughening which is substantially microscopic in character.
- the etched surface produced by the treatment is in much better condition for the reception of organic finishes than the original highly finished surface.
- the etched surface In the preparation of dials for instruments and recorders and similar apparatus, for example, the etched surface will hold a white enamel background lfinish and black enamel indicia much better than the untreated copper alloy.
- the finish will adhere as well nto the electrolytically etched copper base metal as it will to'more expensive alloys heretofore deemed necessary for the purpose.
- FIG. 2 of the drawing there is shown an enlarged sectional view of a plate 50, of brass or the like, with an electrolytically etched surface 54.
- An organic finish 52 is keyed to the plate 50 by the microscopic roughened surface 54.
- the coated unit of Figure 2 constitutes 'a desirable improvement in the art.
- FIG. 4 there is shown photomicrographs at a magnification of about 300X of the surfaces of an alloy of (5W/2% copper, the balance being substantially zinc, after having being electro-etched according tov the present invention and the original cold rolled surface respectively.
- Examination of the photomicrograph of Figure 3 shows that the surface has many iine pits distributed uniformly over the entire surface. The pits are disposed without regard to crystals of the brass, high spots or other gross features. It is these fine pits that provide for good paint adhesion without any roughness apparent in, the paint coating.
- the rolled surface exhibits a relatively smooth structure that does not provide a coating of paint means to effect a good bond thereto.
- a sheet of brass his inch thick had half of its surface etched while the other half remained unaltered.
- the entire member was then coated with a standard white lacquer and the coated metal baked to harden the organic lacquer.
- the opposite edges of the coated sheet were then bent substantially back upon themselves with the organic nish being upon the external side of the bend.
- the organic finish did not flake off or indicate any'other evidence of failure at the bend.
- the organic finish had been applied to the unetched surface the organic finish was cracked and small flakes had become disrupted.
- the method of electroetching the surface of a copper base alloy member containing at least 60% copper comprising making the member the anode in an electrical circuit, applying to the surface of the member an aqueous electrolyte having as its essential ingredients from 20% to 85% by weight of phosphoric acid, from 25% to 0.1% by weight of nitric acid and the balance water, and passing an electrical current through the circuit including the member and the aqueous electrolyte to etch the surface of the member to produce a substantially uniform microscopic roughening and pitting of the surface to enable organic finishes to adhere more tenaciously.
- the method of electroetching the surface of a-copper base alloy member containing at least 60% copper comprising making the member the anode in an electrical circuit, applying to the surface of the member an aqueous electrolyte having as its essential ingredients from 20% to 85% by weight of phosphoric acid, from 25% to 0.1% by weight of nitric acid and the balance water, and passing an electrical current of from 20 to 100 amperes per square foot of surface of the member through the circuit including the member and the aqueous electrolyte to etch the surface of the member to produce a substantially uniform microscopic roughening and pitting of the surface to enable organic finishes to adhere more tenaciously.
- the method of electroetching the surface of a copper base alloy member containing at least 60% copper, the alloy having impurities therein tending to form a surface smut on etching comprising making the member the anode in an electrical circuit, applying to the surface of a member an aqueous electrolyte having as its essential ingredients from 20% to 85% by weight of phosphoric acid, from 25% to 0.1% nitric acid, from effective amounts up to by weight of a water soluble oxidizing compounds of chromium and oxygen selected from the group consisting of chromates, dichromates and chromic acid to oxidize the impurities that would otherwise form a smut and the balance water, and passing an electrical current throughthe circuit including the member and the aqueous electrolyte to etch the surface of the member to produce a substantially uniform microscopic roughening and pitting of the surface to enable organic finishes to adhere more tenaciously.
- the method of electroetching the surface of a copper base alloy member containing at least 60% copper, the alloy having impurities therein tending to form a surface smut on etching comprising making the member the anode in an electrical circuit, applying to the surface of the member an aqueous electrolyte having as its essential ingredients from 20% to 85% by weight of phosphoric acid, from to 0.1% nitric acid, from effective amounts up to 5%.by weight of a water soluble oxidizing compound of chromium and oxygen selected from the group consisting of chromates, dichromates and chromic acid to oxidize the impurities that would otherwise form a smut and the balance water, and passing an electrical current of from 20 to 100 amperes per square foot of surface of the member through the circuit including the member and the aqueous electrolyte to etch the surface of the member to produce a substantially uniform microscopic roughening and pitting of the surface to enable organic finishes to adhere more tenaciously.
Description
Feb 22, l949 G. w. JERNsTED-r ETCHING METHOD 2 Sheets-Sheet `Il.
Filed Sept. 27, 1944 INVENTOR ATT WITNESSES:
9- G. w. JERNSTEDT 2,462,197
ETCHING METHOD Feb. 22, 19
Filed Sept. 27, 1944 2 Sheets-Sheet 2 Fig 3.
wlTNEssEs.- INVENTOR @[M George WJnszedz.
Patented Feb. 22, 1949 UNITED STATES PATENT lG'FliIC-E y 2,462,197 Eremo METHOD George W. Jernstedt, Belleville, N. J., assigner to Westinghouse Electric Corporation, East Pittsburgh, Pa., a corporation of Pennsylvania Applicationseptember 27, 1944, SerialNo.f555,979
4 Claims.
is ordinarily not entirely satisfactory. Brightly finished brass sheet, for example, when coated with enamels or lacquers and subjected to bending or further rWorking loses the adhesion of the enamel or lacquer to the brass surface with consequent iiaking of the organic finish. Even in cases where the organic finish does not akeoff the brass on bending, the bond becomes so Weak- `ened that a slight rubbing or scratching Will cause the organic finish to flake off readily.
The object of this invention is to provide for treating metal surfaces to produce a surface .structure for better adhesion of Aorganic nishes. `Other objects of the invention will in part be obvious and will inpart appear hereinafter.
For a fuller understanding of the nature and objectsI of the invention, reference may be had to the following ydetailed description, taken in conjunction with the accompanying drawing, in which:
Figure 1 is a schematic elevational view of an apparatus for carrying out the invention;
Fig. 2 is a fragmentarysectional view showing a metal sheet provided with an organic finish;
Fig. 3 i-s a photomicrograph of the surface of a sheetof brass treated according to the invention; and
Fig. 4 is a photomicrograph of the surface -of la. sheet of untreated cold rolled brass.
In the production of smooth nished copper .alloy sheets, such as brass sheets for example, the sheet metal is frequently subjected to cold rolling and other surfacetreatment which results in a smooth surface but which Vhas insuflicient tooth or roughness for the best advvhesicn of subsequent Yorganic linish coatings. It Ais desirable, on the other hand, in fabricating members from such `copper base alloys, to apply to :the member some decorative iinish. Ordinary sprayed or brushed paint and lacquer coatings when vapplied to highly fini-shed copper base alloy-sheets do not 4adhere to the metal. with sufficient tenacity to insure .an adequate life for the finish. Where the .member is subjected to .slight bending or tensile stresses, thel finish will either .crack and flake :off .orelse lose its adhesion to the copper base sheet and ,upon b eingfsubjected to slight mechanical :abrasion willqeasily beremoved. The failureof the organicinsh is undesirable. Accordingly the manutaetureris frequently forced to substitute'metals which are more expensive than copper base alloys lider to avoid this objectionable feature.
According to this invention copper :base ,alloys in the form of sheets, machined parts, vforgings and other smooth surfaced shapes are subjected to an'electrolytic treatment Wherebi7 ,the surface of the metal is given a tooth ormicroscopic roughening suiicient f or a greatly enhanced ad.-
herence of organic finishes. When provided with such a surface, the metal may be bent and subjected to ,other stresses without premature failure of the coating of Vorganic finish by flaking and the like. Furthermore, the organic iinishpnplectrclytically treated surfaces vwill withstand considerably more abrasion before lossof the organic vfinish than on untreated surfaces.
In some cases vshot or sand blasting ,offcopper alloy sheets has been resorted to in orderftp prepare a better surface forzsubsequent coating-s of organic finish. Shot blasting-.Will ,distort thin sheet metal and damagedelicate members Whereas electroetching can be safely appl-iedto the thinnest sheets and -most fragile Aparts. ther the shot or sand blasting isr not always form. 4In many Vcases the treatment ,of .copper alloy electrolytically isless expensive. y
Briefly the electrolytic treatmentccmprises lthe anodic etching of copper base alloymembersin an aqueous solutionofphosphoric acid and nitric acid. This treatment Willproduce a suiiicient microscopic alteration ,of the metal to rougher; and pit the surface vto provide a `greatly improved adherence .of organic `finishes. togthe surface.
In carrying out the process, reference should behad to- Fig. 1 showing a suggested Imode of treating copper base metals. Other Possible modes and forms ;of apparatus will Ahecht/,ions to those skilled inthe art. The apparatus `ll f .for carrying out the etohingpperation includes an endless conveyor tracky l2 whereby-copper Vbase members to `be electrolytically etchedaare carried through the entire process of operations. VAt portion .1li .of the conveyor I2 is lccatedf a loading statio-nfor loading articles 38 iiponcon veyors zfonsubsequent processing.' The'gmembers 38 are suspended upon hooks 3,2 of the conveyor 28 provided'with Wheel-S30 for-travelalong track l2. When the wheeled conveyors .gtrayel .from Yloafilinsstation .14 of track .1.2, them-,ap-
. volume of one gallon.
makes contact with an anode bar 35 whereby electrical current flowsfrom the bar 36 to contact 34 through conveyor 28 to the hook 32 and thence to the member 38 to be etched. After each conveyor 28 has remained a predetermined length of time upon portion I8 of the track I2, the conveyors are caused to move upwardly along rise 20 of the track.
Passing further the conveyors 28 descend on portion 22 of the track to a lower horizontal portion 24 whereby the members 38 are dipped into a water wash solution 48 contained Within tank 46. The wash solution 48 removes the etching acids. The members 38 are then brought up out of the wash solution to the unloading portion 26 of the track l2. After drying in an oven or by other suitable means, the members are in condition for further processing.
The etching solution tank 48 is made the cathode by connecting thereto a direct current cathode conductor 44 to a portion of the tank 48. The tank 40 is made of some conducting metal which will be resistant Ito the etching solution. A lead liner, for example, is satisfactory for the purpose, but steel cathode liners are preferred.
The etching solution 42 is an equeous electrolyte containing from 20% to 85% phosphoric acid (H3PO4) by weight from 0.1% to 25% nitric acid by weight. The solutions with higher concentrations of phosphoric acid are employed for copper base metals which contain the higher percentages of copper.
The main function of the nitric acidin the electrolytic solution appears to be to remove a surface layer of soft non-adherent copper parfticles which form during'the electrolytic treatment.
The electrolyte of phosphoric acid and nitric acid operates satisfactorily when applied to copper base alloys having substantially no impurities, particularly metallic impurities such as lead, arsenic, and iron. If these metallic impurities are present in the copper base alloy, 'a surface smut may be left on the electro-etched copper alloy. It has been found that the additionof oxidizing compounds of chromium and oxygen, such for example, as chromic acid, sodium chromate and potassium dichromate, to the electrolyte will prevent formation of the smut. The amount of the chromium and oxygen compound may be as much as of the weight of the bath.
In operating the etching bath it has been discovered that best results are obtained when the amperage per square foot of surface being treated varies between 20 and 100 amperes. With current of this strength, a good etch for the subsequent application of organic finishes is obtained in from 2 to 10 minutes. Four minutes of treatment has been found in many cases to produce highly effective results.
In treating a relatively pure brass composed of 671/2% copper, the balance being substantially all zinc, the electrolyte solution was prepared from 1450 milliliters of 85% Hal-O4 and 150 milliliters of 70% HNOa diluted with Water -to Ia roughly 45% by weight phosphoric acidand 3% by weight nitric acid,
In the treatment of a. relatively impure 40-60 The solution containedbrass, for example, a solution having 50% phos-4 phoric acid, 1% nitricacid and 1/2% potassium dichromate by weight gave a highly effective etch in four minutes at a current density of 40 amperes per square foot.
The proportions of the electrolyte composition obviously may bermodifled for different amounts and kinds of impurities and the copper base alloys being subjected to the treatment.
After the copper base alloy metal has been electrolytically etched, washed and dried, an examination of the surface will reveal a marked dulling of the original bright finish due mainly to the fact that the surface has Ibeen preferentially etched to produce a roughening which is substantially microscopic in character. The etched surface produced by the treatment is in much better condition for the reception of organic finishes than the original highly finished surface. In the preparation of dials for instruments and recorders and similar apparatus, for example, the etched surface will hold a white enamel background lfinish and black enamel indicia much better than the untreated copper alloy. The finish will adhere as well nto the electrolytically etched copper base metal as it will to'more expensive alloys heretofore deemed necessary for the purpose.
Referring to Figure 2 of the drawing, there is shown an enlarged sectional view of a plate 50, of brass or the like, with an electrolytically etched surface 54. An organic finish 52 is keyed to the plate 50 by the microscopic roughened surface 54. The coated unit of Figure 2 constitutes 'a desirable improvement in the art.
Referring to Figures and 4, there is shown photomicrographs at a magnification of about 300X of the surfaces of an alloy of (5W/2% copper, the balance being substantially zinc, after having being electro-etched according tov the present invention and the original cold rolled surface respectively. Examination of the photomicrograph of Figure 3 shows that the surface has many iine pits distributed uniformly over the entire surface. The pits are disposed without regard to crystals of the brass, high spots or other gross features. It is these fine pits that provide for good paint adhesion without any roughness apparent in, the paint coating. In Figure 4 the rolled surface exhibits a relatively smooth structure that does not provide a coating of paint means to effect a good bond thereto. vThe difference in iiatness between the surfaces is imperceptible except` under a microscope. Visually the electro-etched surface of Figure 3 has a dull appearance as compared to that of Figure 4. It is believed 'that no treatment known to the art heretofore etched to roughen the metal surface without regard to crystal structure by etching pits over the entire surface as uniformly as shown in the'photomicrograph of Figure 3.
The following is illustrative of the improvement in adhesion secured by the invention. A sheet of brass his inch thick had half of its surface etched while the other half remained unaltered. The entire member was then coated with a standard white lacquer and the coated metal baked to harden the organic lacquer. The opposite edges of the coated sheet were then bent substantially back upon themselves with the organic nish being upon the external side of the bend. In the case where the etching has been employed, the organic finish did not flake off or indicate any'other evidence of failure at the bend. On the other hand where the organic finish had been applied to the unetched surface the organic finish was cracked and small flakes had become disrupted. Lightly rubbing the organic finish at the bend with the iingernail failed to remove any of the lacquer from the etched metal portion while on the unetched metal the lacquer came off easily and freely. A great improvement in the adhesion of the organic nish for the metal has thus been secured by electrolytically etching the surface.
Since certain changes may be made in the above invention and different embodiments of the invention could be made without departing from the scope thereof, it is intended that all matter contained in the above description or taken in connection with the accompanying drawings shall be interpreted as illustrative and not in a limiting sense.
I claim as my invention:
1. The method of electroetching the surface of a copper base alloy member containing at least 60% copper comprising making the member the anode in an electrical circuit, applying to the surface of the member an aqueous electrolyte having as its essential ingredients from 20% to 85% by weight of phosphoric acid, from 25% to 0.1% by weight of nitric acid and the balance water, and passing an electrical current through the circuit including the member and the aqueous electrolyte to etch the surface of the member to produce a substantially uniform microscopic roughening and pitting of the surface to enable organic finishes to adhere more tenaciously.
2. The method of electroetching the surface of a-copper base alloy member containing at least 60% copper comprising making the member the anode in an electrical circuit, applying to the surface of the member an aqueous electrolyte having as its essential ingredients from 20% to 85% by weight of phosphoric acid, from 25% to 0.1% by weight of nitric acid and the balance water, and passing an electrical current of from 20 to 100 amperes per square foot of surface of the member through the circuit including the member and the aqueous electrolyte to etch the surface of the member to produce a substantially uniform microscopic roughening and pitting of the surface to enable organic finishes to adhere more tenaciously.
3. The method of electroetching the surface of a copper base alloy member containing at least 60% copper, the alloy having impurities therein tending to form a surface smut on etching, comprising making the member the anode in an electrical circuit, applying to the surface of a member an aqueous electrolyte having as its essential ingredients from 20% to 85% by weight of phosphoric acid, from 25% to 0.1% nitric acid, from effective amounts up to by weight of a water soluble oxidizing compounds of chromium and oxygen selected from the group consisting of chromates, dichromates and chromic acid to oxidize the impurities that would otherwise form a smut and the balance water, and passing an electrical current throughthe circuit including the member and the aqueous electrolyte to etch the surface of the member to produce a substantially uniform microscopic roughening and pitting of the surface to enable organic finishes to adhere more tenaciously.
4. The method of electroetching the surface of a copper base alloy member containing at least 60% copper, the alloy having impurities therein tending to form a surface smut on etching, comprising making the member the anode in an electrical circuit, applying to the surface of the member an aqueous electrolyte having as its essential ingredients from 20% to 85% by weight of phosphoric acid, from to 0.1% nitric acid, from effective amounts up to 5%.by weight of a water soluble oxidizing compound of chromium and oxygen selected from the group consisting of chromates, dichromates and chromic acid to oxidize the impurities that would otherwise form a smut and the balance water, and passing an electrical current of from 20 to 100 amperes per square foot of surface of the member through the circuit including the member and the aqueous electrolyte to etch the surface of the member to produce a substantially uniform microscopic roughening and pitting of the surface to enable organic finishes to adhere more tenaciously.
GEORGE W. JERNSTEDT.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,069,151 Loewenthal Aug. 5, 1913 1,946,647 Taylor et al Feb. 13, 1934 1,946,766 Shonkwiler et al. Feb. 13, 1934 2,142,024 I-Iall Dec. 27, 1933 2,182,244 Beall Dec. 5, 1939 OTHER REFERENCES
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US555979A US2462197A (en) | 1944-09-27 | 1944-09-27 | Etching method |
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US555979A US2462197A (en) | 1944-09-27 | 1944-09-27 | Etching method |
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US2462197A true US2462197A (en) | 1949-02-22 |
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US555979A Expired - Lifetime US2462197A (en) | 1944-09-27 | 1944-09-27 | Etching method |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2553937A (en) * | 1948-01-17 | 1951-05-22 | Alais & Froges & Camarque Cie | Method of electrolytically polishing aluminum and its alloys |
US2626589A (en) * | 1948-12-01 | 1953-01-27 | Gen Motors Corp | Electrostatic spray painting apparatus |
US2872387A (en) * | 1948-05-12 | 1959-02-03 | Kolodney Morris | Anodic treatment of uranium |
US3103481A (en) * | 1963-09-10 | Electrolytic cell | ||
US4746416A (en) * | 1986-03-07 | 1988-05-24 | Western Industries Inc. | Hanger for use in electrocoating |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1069151A (en) * | 1912-12-16 | 1913-08-05 | Jacques Loewenthal | Process for the production of an insulating-coating on electrical conductors. |
US1946647A (en) * | 1932-05-25 | 1934-02-13 | Eastman Kodak Co | Process of coating copper with cellulose acetate lacquer |
US1946766A (en) * | 1933-04-08 | 1934-02-13 | Albert H Shonkwiler | Finishing ferrous sheet material |
US2142024A (en) * | 1936-09-30 | 1938-12-27 | Egyptian Lacquer Mfg Company | Coating surfaces of zinc-base |
US2182244A (en) * | 1936-10-15 | 1939-12-05 | Frank H Beall | Chromium plating |
-
1944
- 1944-09-27 US US555979A patent/US2462197A/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1069151A (en) * | 1912-12-16 | 1913-08-05 | Jacques Loewenthal | Process for the production of an insulating-coating on electrical conductors. |
US1946647A (en) * | 1932-05-25 | 1934-02-13 | Eastman Kodak Co | Process of coating copper with cellulose acetate lacquer |
US1946766A (en) * | 1933-04-08 | 1934-02-13 | Albert H Shonkwiler | Finishing ferrous sheet material |
US2142024A (en) * | 1936-09-30 | 1938-12-27 | Egyptian Lacquer Mfg Company | Coating surfaces of zinc-base |
US2182244A (en) * | 1936-10-15 | 1939-12-05 | Frank H Beall | Chromium plating |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3103481A (en) * | 1963-09-10 | Electrolytic cell | ||
US2553937A (en) * | 1948-01-17 | 1951-05-22 | Alais & Froges & Camarque Cie | Method of electrolytically polishing aluminum and its alloys |
US2872387A (en) * | 1948-05-12 | 1959-02-03 | Kolodney Morris | Anodic treatment of uranium |
US2626589A (en) * | 1948-12-01 | 1953-01-27 | Gen Motors Corp | Electrostatic spray painting apparatus |
US4746416A (en) * | 1986-03-07 | 1988-05-24 | Western Industries Inc. | Hanger for use in electrocoating |
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