US3186870A - Process for removing thin films of cobalt oxide from vitreous surfaces - Google Patents
Process for removing thin films of cobalt oxide from vitreous surfaces Download PDFInfo
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- US3186870A US3186870A US59142A US5914260A US3186870A US 3186870 A US3186870 A US 3186870A US 59142 A US59142 A US 59142A US 5914260 A US5914260 A US 5914260A US 3186870 A US3186870 A US 3186870A
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- Prior art keywords
- phosphoric acid
- ferrous
- film
- cobalt oxide
- temperature
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- 229910000428 cobalt oxide Inorganic materials 0.000 title claims description 14
- 238000000034 method Methods 0.000 title claims description 14
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 title description 12
- 239000010409 thin film Substances 0.000 title description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 58
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 29
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims description 16
- 229910001448 ferrous ion Inorganic materials 0.000 claims description 15
- 239000007864 aqueous solution Substances 0.000 claims description 6
- UBEWDCMIDFGDOO-UHFFFAOYSA-N cobalt(2+);cobalt(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[Co+2].[Co+3].[Co+3] UBEWDCMIDFGDOO-UHFFFAOYSA-N 0.000 claims description 2
- 239000010408 film Substances 0.000 description 33
- 235000003891 ferrous sulphate Nutrition 0.000 description 14
- 239000011790 ferrous sulphate Substances 0.000 description 14
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 14
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 14
- 239000000243 solution Substances 0.000 description 12
- 239000011521 glass Substances 0.000 description 11
- 239000002253 acid Substances 0.000 description 10
- 229960002089 ferrous chloride Drugs 0.000 description 9
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 description 9
- -1 ferrous compound Chemical class 0.000 description 7
- 150000002736 metal compounds Chemical class 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 238000012217 deletion Methods 0.000 description 2
- 230000037430 deletion Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000012224 working solution Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000005357 flat glass Substances 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000005341 toughened glass Substances 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- G02B5/208—Filters for use with infrared or ultraviolet radiation, e.g. for separating visible light from infrared and/or ultraviolet radiation
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C23/00—Other surface treatment of glass not in the form of fibres or filaments
Definitions
- the present invention relates broadly to films of metal compounds and more particularly to the removal of such films from surfaces to which they have been applied.
- Ultra-thin, transparent films of metal compounds, particularly the oxides and to some extent the fluorides, have recently come into rather wide use for a number of purposes ranging from electrical conductivity to light modification.
- the primary object of this invention is to provide a novel and improved way in which part or all of an ultra-thin film can be removed from its supporting base.
- a more specific object is the provision of a method of removing metal compound film from vitreous surfaces.
- a still more specific object is to provide a procedure for removing thin, transparent cobalt oxide films from glass surfaces.
- the single figure is a graphic comparison of the removal times and temperatures for removal agents of different compositions.
- the process of the present invention is effected by subjecting a surface, filmed with a metal compound, to a heated aqueous solution of phosphoric acid containing a small percentage of a film solution accelerator, namely a ferrous ion.
- a ferrous ion may be supplied by means of a suitable ferrous compound of appropriate solubility and it has been found that ferrous Fatented June 1, 1965 'ice sulfate and ferrous chloride are satisfactory for this purpose.
- the concentration of phosphoric acid may be in the range from 50 weight percent to 85 weight percent; and, it has been found desirable to practice the invention at an acid concentration of about to percent. Any grade of phosphoric acid of the desired concentration may be employed. However, we have preferred to use technical grade phosphoric acid which contains 85% acid and has a specific gravity of 1.689 (11.98 pounds per gallon).
- the ferrous ion may be employed in a range from about 0.25% to about 5.0% based on the weight of the phosphoric acid.
- the upper limit of ferrous ion is determined by the solubility in phosphoric acid of the ferrous compound employed to furnish the ferrous ion. For example, at 266 F., ferrous sulfate is soluble in 85% phosphoric acid to the extent of 1.6% iron; ferrous chloride is soluble to the extent of 4.8% iron at this temperature.
- compositions of the present invention are all temperature dependent.
- curve A the time in seconds to remove a 30% transmitting film of cobalt oxide is plotted against the acid temperature; a 30% transmitting film of cobalt oxide transmits 30% of Illuminant C (artificial daylight).
- Illuminant C artificial daylight
- the film removing composition is suitably made by adding the ferrous compound as a concentrated aqueous solution to the aqueous phosphoric acid.
- the Water in which the ferrous compound is dissolved will evaporate when the acid solution is heated to an operating temperature of about 250 F.
- ferrous compound is ferrous sulfate
- the addition of solid ferrous sulfate to the phosphoric acid to form the film removing solution is to be avoided since ferrous sulfate is only slowly soluble in phosphoric acid. Also a 1% concentration of ferrous sulfate is recommended as a working figure because of the possibility that higher concentrations may recrystallize on cooling.
- ferrous compound is ferrous chloride
- the addition of solid ferrous chloride to the phosphoric acid to form the film removing composition is practicable due to the higher solubility in the phosphoric acid.
- Higher concentrations of ferrous chloride depending upon acid concentration and temperature, can also be employed in contrast to the ferrous sulfate due to the higher solubility of the ferrous chloride.
- Ferrous sulfate is soluble in water at room temperature (70 F.) to the extent of 1.2 pounds per gallon.
- the aqueous ferrous sulfate addition solution can therefore be made up to this concentration.
- one gallon of the addition agent may be employed for every gallons or 120 pounds of 85 phosphoric acid to make a working solution containing 1% by weight of ferrous sulfate. This will provide approximately 0.3% ferrous ion in the solution.
- ferrous chloride (FeCl -4I-I O) is solu- Ible in water at 50 F, to the extent of approximately 14 pounds per gallon.
- the aqueous ferrous chloride addition solution can therefore be made up to this concentration.
- one gallon of the addition agent may be employed for every 23.3 gallons or 280 pounds of 85% phosphoric acid to make a working solution containing about 5% by weight of ferrous chloride. This will provide approximately 1.5% of ferrous ion in the solution.
- the ferrous ion is slowly exhausted as filmed glass is treated in the bath.
- the ferrous ion concentration can be maintained substantially constant by adding a suitable amount of the ferrous compound to the phosphoric acid make-up which is required to replace that removed by the deleted lights;
- the curve A shown in FIG. 1 represents the times required for completely deleting a transmitting cobalt oxide film.
- many automobile back windows are rejected because of spots, which are heavy deposits of cobalt oxide. These spots usually require 2 to 3 times the deleting time of the film.
- Example I Removal rates of FIG. 1 were plotted by making a series of runs wherein a bath of aqueous phosphoric acid of a concentration of 85 weight percent acid, and containing 1% by Weight of ferrous sulfate, was heated at increasing temperature increments in the range from about 140 F. to about 350 F.
- curve A shows that the combination of phosphoric acid and ferrous sulfate is about 30 times faster than phosphoric acid at the same temperature.
- the invention is applicable to the treatment of both tempered and untempered glass.
- the thermal shock encountered when treating tempered glass of room temperature will be harmless.
- the invention is applicable to the removal of films from vitreous surfaces in general, including glass, quartz, porcelain and the like.
- a process for removing a film of cobalt oxide from a vitreous surface including the steps of, providing a bath made up of an aqueous solution of phosphoric acid of a concentration in the range from about 50 to about 85% by weight and ferrous ion equal to at least 0.5% by weight of the phosphoric acid, said ferrous ion being supplied by adding ferrous sulfate to said acid, heating said bath to a temperature in the range from about 140 F. to about 350 F., subjecting said filmed surface to said bath for a time sufiicient to remove the film, and removing the solution from the vitreous surface.
- a process for removing a film of cobalt oxide from a vitreous surface including the steps of, providing a bath made up of an aqueous solution of phosphoric acid of a concentration in the range from about 50 to about 85% by weight and ferrous ion equal to at least 0.5% by weight of the phosphoric acid, said ferrous ion being supplied by adding ferous chloride to said acid, heating said bath to a temperature in the range from about 140 F. to about 350 F., subjecting said filmed surface to said bath for a time sufiicient to remove the film, and removing the solution from the vitreous surface.
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- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Engineering & Computer Science (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Surface Treatment Of Glass (AREA)
Description
June 1, 1965 R. G. MENTZER 3,186,870
PROCESS FOR REMOVING THIN FILMS OF COBALT OXIDE FROM VITREOUS SURFACES Filed Sept. 22, 1960 Txme 1n Seconds Temper=dtcme in Deg' ees-F IN V EN TOR.
A TTORNE YS United States Patent 3 186 87 0 PROCESS FOR REMGVHNG FILMS 0F COBALT OXlDE FRQM VITREGUS SURFACES Robert G. Mentzer, Toledo, Ohio, assignor to Libbeytlwens-Ford Glass Company, Toledo, Ohio, a corporatlon of Ohio Filed Sept. 22, 1960, Ser. No. 59,142 6 Claims. (Cl. 134-3) The present invention relates broadly to films of metal compounds and more particularly to the removal of such films from surfaces to which they have been applied.
This application is a continuation-in-part of my copending application Serial No. 841,724, now abandoned filed September 23, 1959.
Ultra-thin, transparent films of metal compounds, particularly the oxides and to some extent the fluorides, have recently come into rather wide use for a number of purposes ranging from electrical conductivity to light modification.
By way of example only, it may be mentioned that certain light modifying films have recently found an important place in the automotive industry. This arose from the fact that in the present-day large area rear Wmdows or backlights for automobiles, passengers experience considerable discomfort from the suns rays through the unusual expanse of glass which extends well into the roof of the car.
In order to overcome this problem it has been proposed to apply a film, such as a very thin cobalt oxide film, along the upper area of the rear window to reduce the transmission of objectionable components of the suns rays while at the same time preserving a substantial amount of visibility through the window.
However, there are instances where it is found upon critical inspection, after it has been applied, that the film is not sufficiently perfect for commercial acceptance. In this event, removal of the film is desirable so that the expensive bent, polished plate glass window need not be scrapped but may be reprocessed to produce a new backlight with a satisfactory film. There are also instances where it is necessary or desirable to delete portions of thin films from selected areas only of a filmed or partially filmed base or to remove part of a film in order to reduce its thickness.
Accordingly, the primary object of this invention is to provide a novel and improved way in which part or all of an ultra-thin film can be removed from its supporting base.
A more specific object is the provision of a method of removing metal compound film from vitreous surfaces.
A still more specific object is to provide a procedure for removing thin, transparent cobalt oxide films from glass surfaces.
Further objects and advantages of the invention will become more apparent during the course of the following description when taken in connection with the accompanying drawings.
In the drawings, wherein like numerals are employed to designate like part throughout the same:
The single figure is a graphic comparison of the removal times and temperatures for removal agents of different compositions.
Broadly speaking, the process of the present invention is effected by subjecting a surface, filmed with a metal compound, to a heated aqueous solution of phosphoric acid containing a small percentage of a film solution accelerator, namely a ferrous ion. The ferrous ion may be supplied by means of a suitable ferrous compound of appropriate solubility and it has been found that ferrous Fatented June 1, 1965 'ice sulfate and ferrous chloride are satisfactory for this purpose.
The concentration of phosphoric acid may be in the range from 50 weight percent to 85 weight percent; and, it has been found desirable to practice the invention at an acid concentration of about to percent. Any grade of phosphoric acid of the desired concentration may be employed. However, we have preferred to use technical grade phosphoric acid which contains 85% acid and has a specific gravity of 1.689 (11.98 pounds per gallon).
The ferrous ion may be employed in a range from about 0.25% to about 5.0% based on the weight of the phosphoric acid. The upper limit of ferrous ion is determined by the solubility in phosphoric acid of the ferrous compound employed to furnish the ferrous ion. For example, at 266 F., ferrous sulfate is soluble in 85% phosphoric acid to the extent of 1.6% iron; ferrous chloride is soluble to the extent of 4.8% iron at this temperature.
It is to be understood that, while the present invention is in no way limited to use with films of any specific metal compound or to the removal of films from any specific supporting surface, it has been found to be particularly effective in removing cobalt oxide films from glass and, for purposes of illustration, will be specifically described in that connection here.
The deletion rates of compositions of the present invention are all temperature dependent. In FIG. 1, curve A, the time in seconds to remove a 30% transmitting film of cobalt oxide is plotted against the acid temperature; a 30% transmitting film of cobalt oxide transmits 30% of Illuminant C (artificial daylight). It will be seen that at a temperature of 140 F, approximately seconds are required for a solution containing 85% phosphoric acid and 1% ferrous sulfate to remove the film. On the other hand, at a temperature of 350 F. the deletion time is reduced to approximately 2 seconds. Thus temperatures in the range from F. to 350 F. are within the scope of the present invention. However, for preferred operation, the process is practiced at a temperature in the range from about 212 F. to about 250 F. By so operating, the acid concentration of the treating bath will be retained substantially constant because the water loss therefrom due to evaporation will be approximately negligible.
The film removing composition is suitably made by adding the ferrous compound as a concentrated aqueous solution to the aqueous phosphoric acid. The Water in which the ferrous compound is dissolved will evaporate when the acid solution is heated to an operating temperature of about 250 F.
Where the ferrous compound is ferrous sulfate, the addition of solid ferrous sulfate to the phosphoric acid to form the film removing solution is to be avoided since ferrous sulfate is only slowly soluble in phosphoric acid. Also a 1% concentration of ferrous sulfate is recommended as a working figure because of the possibility that higher concentrations may recrystallize on cooling.
Where the ferrous compound is ferrous chloride, however, the addition of solid ferrous chloride to the phosphoric acid to form the film removing composition is practicable due to the higher solubility in the phosphoric acid. Higher concentrations of ferrous chloride, depending upon acid concentration and temperature, can also be employed in contrast to the ferrous sulfate due to the higher solubility of the ferrous chloride.
Ferrous sulfate is soluble in water at room temperature (70 F.) to the extent of 1.2 pounds per gallon. The aqueous ferrous sulfate addition solution can therefore be made up to this concentration. Thus, one gallon of the addition agent may be employed for every gallons or 120 pounds of 85 phosphoric acid to make a working solution containing 1% by weight of ferrous sulfate. This will provide approximately 0.3% ferrous ion in the solution.
As an example, ferrous chloride (FeCl -4I-I O) is solu- Ible in water at 50 F, to the extent of approximately 14 pounds per gallon. The aqueous ferrous chloride addition solution can therefore be made up to this concentration. Thus one gallon of the addition agent may be employed for every 23.3 gallons or 280 pounds of 85% phosphoric acid to make a working solution containing about 5% by weight of ferrous chloride. This will provide approximately 1.5% of ferrous ion in the solution.
The ferrous ion is slowly exhausted as filmed glass is treated in the bath. However, the ferrous ion concentration can be maintained substantially constant by adding a suitable amount of the ferrous compound to the phosphoric acid make-up which is required to replace that removed by the deleted lights;
The curve A shown in FIG. 1 represents the times required for completely deleting a transmitting cobalt oxide film. However, many automobile back windows are rejected because of spots, which are heavy deposits of cobalt oxide. These spots usually require 2 to 3 times the deleting time of the film.
The novelty of the present invention is highlighted by the following example:
Example I Removal rates of FIG. 1 were plotted by making a series of runs wherein a bath of aqueous phosphoric acid of a concentration of 85 weight percent acid, and containing 1% by Weight of ferrous sulfate, was heated at increasing temperature increments in the range from about 140 F. to about 350 F.
At each temperature level a sheet of glass, containing a 30% transmitting cobalt oxide film was immersed in the bath for the time required for film removal. Thereafter the glass was removed, rinsed and dried. Removal times were plotted against temperature as curve A.
Runs were also made wherein the bath consisted of aqueous phosphoric acid of a concentration of 85 weight percent, with no ferrous sulfate added, Removal times were plotted against temperatures as curve B.
It will be seen from FIG. 1 that the removal rates plotted by curve A are unexpectedly higher than those of phosphoric acid alone in curve B.
Thus curve A shows that the combination of phosphoric acid and ferrous sulfate is about 30 times faster than phosphoric acid at the same temperature.
The invention is applicable to the treatment of both tempered and untempered glass. Generally the thermal shock encountered when treating tempered glass of room temperature will be harmless. However, when treating untempered glass, it may be necessary to heat the glass to about the temperature of the acid bath before immersion to avoidbreakage.
The invention is applicable to the removal of films from vitreous surfaces in general, including glass, quartz, porcelain and the like.
While the invention has been specifically described in its preferred embodiment as immersing a glass sheet 4 film-removing solution to the sheet by spraying, brushing or the like.
It will be understood that this invention is susceptible to modification in order to adapt it to different usages and conditions and accordingly, it is desired to comprehend such modifications within the scope of the appended claims.
I claim:
1. In a process for removing a film of cobalt oxide from a vitreous surface, the steps of subjecting the filmed surface to the action of an aqueous solution of phosphoric acid, in a concentration in the range of about 50 to by weight, with a ferrous ion, in a range from about 0.25% to 5.0% based .on the weight of the phosphoric acid, at a temperature in the range from about F. to about 350 F.
2. A process as defined in claim 1 wherein the solution is at a temperature in the range from about 212 F. to about 350 F.
3. A process for removing a film of cobalt oxide from a vitreous surface including the steps of, providing a bath made up of an aqueous solution of phosphoric acid of a concentration in the range from about 50 to about 85% by weight and ferrous ion equal to at least 0.5% by weight of the phosphoric acid, said ferrous ion being supplied by adding ferrous sulfate to said acid, heating said bath to a temperature in the range from about 140 F. to about 350 F., subjecting said filmed surface to said bath for a time sufiicient to remove the film, and removing the solution from the vitreous surface.
4. A process as defined in claim 3 wherein the bath is heated to a temperature in the range from about 212 F. to about 350 F.
5. A process for removing a film of cobalt oxide from a vitreous surface including the steps of, providing a bath made up of an aqueous solution of phosphoric acid of a concentration in the range from about 50 to about 85% by weight and ferrous ion equal to at least 0.5% by weight of the phosphoric acid, said ferrous ion being supplied by adding ferous chloride to said acid, heating said bath to a temperature in the range from about 140 F. to about 350 F., subjecting said filmed surface to said bath for a time sufiicient to remove the film, and removing the solution from the vitreous surface.
6. A process as defined in claimS wherein the bath is heated to a temperature in the range from about 212 F. to about 350 F.
References Cited by the Examiner UNITED STATES PATENTS 2,337,460 12/43 French 252-79.2 X 2,360,509 10/44 Morgan et a1 134-3 2,465,750 3/49 Reid 1343 2,557,983 6/51 Lindcr 117-8 X 2,606,566 8/52 Tarnopol 11721l X 2,613,141 10/52 Cochran 1343 2,617,742 11/52 Olson 1172ll 2,762,725 9/56 Saunders 1l7211 X r 2,806,000 9/57 S-treicher 134-2 X 2,850,409 9/ 58 Boicey et al 1l7-211 2,692,189 10/ 59 Bo-Shin Ro 134-3 2,977,241 3/61 Oliver et al. 117-50 DONALD H. SYLVESTER, Primary Examiner.
SIDNEY JAMES, CHARLES A, WILLMUTH,
MORR S Q- WOLK, Examiners.
Git-nu.
Claims (1)
1. IN A PROCESS FOR REMOVING A FILM OF COBALT OXIDE FROM A VITREOUS SURFACE, THE STEPS OF SUBJECTING THE FILMED SURFACE TO THE ACTION OF AN AQUEOUS SOLUTION OF PHOSPHORIC ACID, IN A CONCENTRATION IN THE RANGE OF ABOUT 50 TO 85% BY WEIGHT, WITH A FERROUS ION, IN A RANGE FROM ABOUT 0.25% TO 5.0% BASED ON THE WEIGHT OF THE PHOSPHORIC ACID, AT A TEMPERATURE IN THE RANGE FROM ABOUT 140*F. TO ABOUT 350*F.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US59142A US3186870A (en) | 1960-09-22 | 1960-09-22 | Process for removing thin films of cobalt oxide from vitreous surfaces |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US59142A US3186870A (en) | 1960-09-22 | 1960-09-22 | Process for removing thin films of cobalt oxide from vitreous surfaces |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3186870A true US3186870A (en) | 1965-06-01 |
Family
ID=22021105
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US59142A Expired - Lifetime US3186870A (en) | 1960-09-22 | 1960-09-22 | Process for removing thin films of cobalt oxide from vitreous surfaces |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3186870A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3374116A (en) * | 1963-10-03 | 1968-03-19 | Libbey Owens Ford Glass Co | Process for removing thin films from vitreous surfaces |
| US3489624A (en) * | 1965-03-31 | 1970-01-13 | Westinghouse Canada Ltd | Etching techniques for glass |
| WO1995012450A1 (en) * | 1993-11-04 | 1995-05-11 | Tom Miller, Inc. | Humidifier and method for humidifying air |
| US5620503A (en) * | 1993-11-04 | 1997-04-15 | Tom Miller, Inc. | Humidifier and method for humidifying air |
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| US2337460A (en) * | 1942-02-25 | 1943-12-21 | Pittsburgh Plate Glass Co | Formation of thin films upon glass surfaces |
| US2360509A (en) * | 1942-03-04 | 1944-10-17 | Cities Service Oil Co | Pickling solvent |
| US2465750A (en) * | 1944-05-23 | 1949-03-29 | Reid Engineering Company | Composition for preparing aluminum and the like for welding |
| US2557983A (en) * | 1949-03-22 | 1951-06-26 | Pittsburgh Plate Glass Co | Transparent electroconductive article |
| US2606566A (en) * | 1948-01-28 | 1952-08-12 | Pittsburgh Plate Glass Co | Treatment of films with liquid |
| US2613141A (en) * | 1949-07-29 | 1952-10-07 | Aluminum Co Of America | Chemical brightening of aluminum |
| US2617742A (en) * | 1951-12-19 | 1952-11-11 | Pittsburgh Plate Glass Co | Electroconductive article and production thereof |
| US2692189A (en) * | 1952-04-15 | 1954-10-19 | Khe Beng Chiong | Chemical polishing solution and method |
| US2762725A (en) * | 1952-03-14 | 1956-09-11 | Pittsburgh Plate Glass Co | Method of producing a metal film on a refractory base having a metal oxide film thereon |
| US2806000A (en) * | 1956-06-21 | 1957-09-10 | Du Pont | Cleaning stainless steel |
| US2850409A (en) * | 1955-04-25 | 1958-09-02 | Libbey Owens Ford Glass Co | Method of deleting electrically conductive films from a surface |
| US2977241A (en) * | 1959-03-04 | 1961-03-28 | Gen Electric | One coat enamel process |
-
1960
- 1960-09-22 US US59142A patent/US3186870A/en not_active Expired - Lifetime
Patent Citations (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2337460A (en) * | 1942-02-25 | 1943-12-21 | Pittsburgh Plate Glass Co | Formation of thin films upon glass surfaces |
| US2360509A (en) * | 1942-03-04 | 1944-10-17 | Cities Service Oil Co | Pickling solvent |
| US2465750A (en) * | 1944-05-23 | 1949-03-29 | Reid Engineering Company | Composition for preparing aluminum and the like for welding |
| US2606566A (en) * | 1948-01-28 | 1952-08-12 | Pittsburgh Plate Glass Co | Treatment of films with liquid |
| US2557983A (en) * | 1949-03-22 | 1951-06-26 | Pittsburgh Plate Glass Co | Transparent electroconductive article |
| US2613141A (en) * | 1949-07-29 | 1952-10-07 | Aluminum Co Of America | Chemical brightening of aluminum |
| US2617742A (en) * | 1951-12-19 | 1952-11-11 | Pittsburgh Plate Glass Co | Electroconductive article and production thereof |
| US2762725A (en) * | 1952-03-14 | 1956-09-11 | Pittsburgh Plate Glass Co | Method of producing a metal film on a refractory base having a metal oxide film thereon |
| US2692189A (en) * | 1952-04-15 | 1954-10-19 | Khe Beng Chiong | Chemical polishing solution and method |
| US2850409A (en) * | 1955-04-25 | 1958-09-02 | Libbey Owens Ford Glass Co | Method of deleting electrically conductive films from a surface |
| US2806000A (en) * | 1956-06-21 | 1957-09-10 | Du Pont | Cleaning stainless steel |
| US2977241A (en) * | 1959-03-04 | 1961-03-28 | Gen Electric | One coat enamel process |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3374116A (en) * | 1963-10-03 | 1968-03-19 | Libbey Owens Ford Glass Co | Process for removing thin films from vitreous surfaces |
| US3489624A (en) * | 1965-03-31 | 1970-01-13 | Westinghouse Canada Ltd | Etching techniques for glass |
| WO1995012450A1 (en) * | 1993-11-04 | 1995-05-11 | Tom Miller, Inc. | Humidifier and method for humidifying air |
| US5620503A (en) * | 1993-11-04 | 1997-04-15 | Tom Miller, Inc. | Humidifier and method for humidifying air |
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