[go: up one dir, main page]

US3248235A - Anti-tarnish composition for coppercontaining surfaces - Google Patents

Anti-tarnish composition for coppercontaining surfaces Download PDF

Info

Publication number
US3248235A
US3248235A US141292A US14129261A US3248235A US 3248235 A US3248235 A US 3248235A US 141292 A US141292 A US 141292A US 14129261 A US14129261 A US 14129261A US 3248235 A US3248235 A US 3248235A
Authority
US
United States
Prior art keywords
copper
tarnish
abrasive
mercaptan
composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US141292A
Inventor
Donald M Pryor
Louis F Cason
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
3M Co
Original Assignee
Minnesota Mining and Manufacturing Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to BE622957D priority Critical patent/BE622957A/xx
Priority to NL283747D priority patent/NL283747A/xx
Application filed by Minnesota Mining and Manufacturing Co filed Critical Minnesota Mining and Manufacturing Co
Priority to US141292A priority patent/US3248235A/en
Priority to ES280824A priority patent/ES280824A1/en
Priority to SE10116/62A priority patent/SE310529B/xx
Priority to FR910332A priority patent/FR1347705A/en
Priority to CH1126362A priority patent/CH418088A/en
Priority to DK420562AA priority patent/DK113660B/en
Priority to GB36944/62A priority patent/GB956927A/en
Application granted granted Critical
Publication of US3248235A publication Critical patent/US3248235A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23GCLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
    • C23G1/00Cleaning or pickling metallic material with solutions or molten salts
    • C23G1/02Cleaning or pickling metallic material with solutions or molten salts with acid solutions
    • C23G1/10Other heavy metals
    • C23G1/103Other heavy metals copper or alloys of copper
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0043For use with aerosol devices
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F11/00Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • C23F11/08Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
    • C23F11/10Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F11/00Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • C23F11/08Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
    • C23F11/10Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
    • C23F11/16Sulfur-containing compounds
    • C23F11/161Mercaptans

Definitions

  • V W 1 am "m agents or surfactants, Eckeners or VlSCS m/Z' S L/ A 3,248,235 ANTI-TARNISH COMPOSITION FOR COPPER- CONTAINING SURFACES Donald M. Pryor and Louis F. Cason, both of St. Paul,
  • This invention relates to an anti-tarnish composition for treating tarnished copper-containing surfaces and to a method for rendering such surfaces tarnish resistant.
  • Copper-containing surfaces including copper alloys such as bronze, brass, etc.
  • copper cleaners have been suggested for the removal of tarnish deposits, e.g. copper oxides and sulfides.
  • the problem of inhibiting the tarnishing of the cleaned copper-containing surface through the use of di- is to provide a composition which simultaneously cleans copper-containing surfaces and renders such surfaces tarnish resistant for prolonged periods of time.
  • a highly eflicient composition -for cleaning copper-containing surfaces and for rendering such surfaces tarnish resistant over an extended period of time comprises an aliphatic mercaptan of the formula C H SH wherein n is from 12 to 25,
  • aliphatic mercaptans of the above formula provide a thin, colorless, non-oily protective layer on clean copper-containing surfaces, bonding to the copper through the thiol grouping, and that such mercaptans may be incorporated into copper cleaning formulations to provide a protective layer on the copper substrate as the tarnish is effectively removed by the cleaning ingredients.
  • the bond between the copper and the mercaptans is unusually strong, resisting washing with dilute alkaline or acid solutions, and with detergent solutions. of equal importance is the colorless, transparent protective layer of these mercaptan molecules, which does not adversely effect the luster of the copper-containing surface and which does not discolor or embrittle with aging.
  • the film of mercaptan is virtually invisible to the naked eye, the presence of the protective layer may be detected by the hydrophobic or water repellent properties of the protected surface.
  • the acidic cleaners are preferred because of their high efiioiency.
  • the various combinations of acidic ingredi ents suitable for cleaning copper-containing surfaces are well known. Generally, when using acidic cleaning ingredients in aqueous media, a pH of below about 2.5 is preferred.
  • Hydrochloric acid also is also is an effective non-abrasive copper cleaner. Since the anti-tarnish composition must be essentially nonoxidative, stron-g oxidizing acids, such as nitric acid, should not be used. Suitable acids having a pH between 1 and 5, which are water soluble, stable non-oxidizing the tarnish forming compounds. Con'ventionaL copper acids which do not form water insoluble compounds with cleaners frequently contain mild orgz'ifiic'iicids, such" as ESTEZE oT'sulfamic acidf t'ogether with sodium chloride, various surfactants and abrasives.
  • the copper containing surfaces are extremely reactive in contact with the corroding environment. It is therefore preferable, for providing prolonged tarnish resistance, to accomplish the cleaning and the tarnish prevention simultaneously.
  • abrasive containing mercaptan formulations effectively clean and condition the tarnished surface, the concentration or loading" of abrasive required to remove the tarnish deposits tends to remove the protective mercaptan film as it is formed.
  • the presence of non-abrasive copper cleaning ingredients permits the elimination of, or a reduction in,'
  • surfactant particularly the nonionic variety
  • Viscosity acidic media are usually employed.
  • mercaptan or mixture of mereaptans
  • mercaptan conoentration within the 0.5 to 25, preferably 0.5 to 10, weight percent range is particularly effective in formations containing a non-abrasive copper cleaner. Less than about 0.5 percent of mercaptan does not generally provide suflicient tarnish resistance.
  • the most preferred formulations usually contain from about 1 to weight percent of mercaptan, 0.01% to 25% of a weak organic f acid, 0.01% to 25% of an alkali metal halide (e.g., alkali metal chlorides, etc.), 0.05% to 1% of a surfactant, 0 to of an abrasive, sufficient water to emulsify the mercaptan, and sutiicient acid stable thickeners to provide the desired viscosity.
  • a weak organic f acid e.g., alkali metal chlorides, etc.
  • an alkali metal halide e.g., alkali metal chlorides, etc.
  • Example I Test panels of copper and brass were degreased with trichloroethylene and polished with a commercial copper cleaner containing a non-abrasive copper cleaner, i.e., citric acid and sodium chloride, to remove all traces of tarnish. Immediately after cleaning (a water rinse is preferable), the dry copper-containing surfaces were sprayed with a one percent solution of n-octadecane-lthiol in petroleum ether and buffed with a soft cloth. The panels were then exposed to hydrogen sulfide at about 70% relative humidity along with cleaned uncoated control panels. A marked difference in tarnish rate was noticed, the deposits forming on the controls in less than 15 minutes and the coated panels remaining essentially tarnish free for several hours.
  • a commercial copper cleaner containing a non-abrasive copper cleaner i.e., citric acid and sodium chloride
  • Example 11 The procedure of Example I was repeated using nheneicosane-l-thiol instead of n-ocadecane-l-thiol. After exposure to the hydrogen sulfide atmosphere, the control panels (both copper and brass) tarnished in less than 15 minutes, whereas the treated panels were essentially tarnish free for several hours.
  • Example III The following formulation was prepared, the percentages being by weight:
  • Nonionic surfactant 1 Percent Water 60 Colloidal alumina (AlOOH) 3 n-Octadecane-l-mercaptan l0 Citric acid 8 Sodium chloride 8 Abrasive (50% diatomaceous earth and 50% of 240 mesh silica) 10 Nonionic surfactant 1
  • the colloidal alumina thickener was dissolved in water and the temperature raised to C. After mixing the mercaptan and the nonion-ic surfactant and heating to 80 C., the mixture was added to the colloidal alumina solution with high speed mixing, forming a thick creamy emulsion. Once emulsification was complete, the citric acid and the abrasive were added with continued stirring until a homogeneous dispersion was obtained. Then upon adding the sodium chloride, immediate thickening to a. smooth viscous paste occurred.
  • Copper panels were treated with the above formulation using a soft cloth, followed by water rinsing and air drying. Untreated copper panels whch had been cleaned to remove tarnish were used as controls. After immersing both a treated and an untreated panel in a 1% aqueous solution of hydrogen sulfide, the untreated control was observed to tarnish after 5 seconds whereas tarnishing of the treated panel occurred only after about 2 hours. A similar comparative test using a salt bath (5% aqueous sodium chloride) resulted in tarnishing of the untreated control in 30 minutes and no visible tarnishing of the treated panel after two days.
  • a salt bath 5% aqueous sodium chloride
  • Still another comparative test was made by placing both treated and untreated panels in a high temperature (212 F.) oxidative (air) environment, resulting in tarnishing of the untreated control in 10 minutes and tarnishing of the treated panel only after 6 hours.
  • the time reported is the time required for visible signs of tarnish to appear.
  • Example IV Results similar to those in Example III are obtained with the following formulation:
  • copper is used interchangeably with copper-containing and includes, besides copper, such copper-containing alloys as brass, bronze, etc. having significant quantities of copper therein.
  • An aqueous anti-tarnish composition for copper which consists essentially of 0.01% to 25% of a weak organic acid, 0.01% to 25% of an alkali metal halide, 0.05% to 1% of a surfactant, 0 to 20% of abrasive, and 1 to 15% of a mercaptan of the formula where n is an integer from 12 to 25, the pH of said composition being below about 2.5.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Detergent Compositions (AREA)
  • Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)

Description

I V W 1:. am "m agents or surfactants, Eckeners or VlSCS m/Z' S L/ A 3,248,235 ANTI-TARNISH COMPOSITION FOR COPPER- CONTAINING SURFACES Donald M. Pryor and Louis F. Cason, both of St. Paul,
Minn., assignors to Minnesota Mining and Manufacturing Company, St. Paul, Minn., a corporation of Delaware No Drawing. Filed Sept. 28, 1961, Ser. No. 141,292
6 Claims. (Cl. 106-3) This invention relates to an anti-tarnish composition for treating tarnished copper-containing surfaces and to a method for rendering such surfaces tarnish resistant.
Copper-containing surfaces, including copper alloys such as bronze, brass, etc., are notoriously susceptible to discoloration due to tarnishing of the copper. A great variety of copper cleaners have been suggested for the removal of tarnish deposits, e.g. copper oxides and sulfides. However, the problem of inhibiting the tarnishing of the cleaned copper-containing surface through the use of di- A further object is to provide a composition which simultaneously cleans copper-containing surfaces and renders such surfaces tarnish resistant for prolonged periods of time.
Yet another object is to provide a process for both cleaning and rendering copper-containing surfaces tarnish resist-ant.
Other objects and advantages will become apparent from the following description.
In accordance with this invention, a highly eflicient composition -for cleaning copper-containing surfaces and for rendering such surfaces tarnish resistant over an extended period of time comprises an aliphatic mercaptan of the formula C H SH wherein n is from 12 to 25,
preferably from 16 to 21, and at least one non-abrasive copper cleaning ingredient. If desired r als ma ed to the compo no u ing suspending k e. The adv a I 0 e 1 workers skilled in the art are considered to come within the contemplation of this invention.
In cleaning copper-containing surfaces various nonabrasive ingredients have been used to chemically remove mselves to United States Patent 0 3,248,235 Patented Apr. 26, 1966 the abrasive content of the formulation and provides significantly more effective tarnish resistance and a more efiicient utilization of the mercaptan compound.
It has now been found that aliphatic mercaptans of the above formula provide a thin, colorless, non-oily protective layer on clean copper-containing surfaces, bonding to the copper through the thiol grouping, and that such mercaptans may be incorporated into copper cleaning formulations to provide a protective layer on the copper substrate as the tarnish is effectively removed by the cleaning ingredients. The bond between the copper and the mercaptans is unusually strong, resisting washing with dilute alkaline or acid solutions, and with detergent solutions. of equal importance is the colorless, transparent protective layer of these mercaptan molecules, which does not adversely effect the luster of the copper-containing surface and which does not discolor or embrittle with aging. Moreover, although the film of mercaptan is virtually invisible to the naked eye, the presence of the protective layer may be detected by the hydrophobic or water repellent properties of the protected surface.
Both branched and straight chain aliphatic mercaptans may be employed, although the straight chain mercaptans 5 are preferred. Mercaptans having less than twelve carbon atoms are not as desirable because of their somewhat greater volatility and greater difficulty in formulating with other desired cleaning ingredients. Mercaptans having more than twenty-five carbon atoms are not as desirable because they are higher melting solids and are more difficult to formulate. In general, these mercaptans have a mild odor which, if desired, may be masked with a suitable odorizer. They are non-toxic, particularly when considering the extremely minute quantities that are retained on the copper surface. Illustrative of the preferred mercaptans are n-hexadecane-l-thiol, n-dodecane-l-thiol, noctadecane-l-thiol, n-beneicos-ane-l-thio (C H SH), etc.
Of the many non-abrasive copper cleaning ingredients which do not react with these mercaptans and which may be used in the anti tarnish compositions of this invention the acidic cleaners are preferred because of their high efiioiency. The various combinations of acidic ingredi ents suitable for cleaning copper-containing surfaces are well known. Generally, when using acidic cleaning ingredients in aqueous media, a pH of below about 2.5 is preferred. The combination of a weak acid, e.g., citric acid, sulfamic aci cl, etc., and an alka 1 meta a e, efgf, sodium chloride, potassium chloride, etc., is an effective non-abrasive tarnish remover. Hydrochloric acid also is also is an effective non-abrasive copper cleaner. Since the anti-tarnish composition must be essentially nonoxidative, stron-g oxidizing acids, such as nitric acid, should not be used. Suitable acids having a pH between 1 and 5, which are water soluble, stable non-oxidizing the tarnish forming compounds. Con'ventionaL copper acids which do not form water insoluble compounds with cleaners frequently contain mild orgz'ifiic'iicids, such" as ESTEZE oT'sulfamic acidf t'ogether with sodium chloride, various surfactants and abrasives. After dissolution of the tarnish deposits by the non-a5rasive copper cleaning in gredients, which are usually acidic, and dislodging im- 0 bedded tarnish by abrasive and/or surfactant action, if desired, the copper containing surfaces are extremely reactive in contact with the corroding environment. It is therefore preferable, for providing prolonged tarnish resistance, to accomplish the cleaning and the tarnish prevention simultaneously. Moreover, although abrasive containing mercaptan formulations effectively clean and condition the tarnished surface, the concentration or loading" of abrasive required to remove the tarnish deposits tends to remove the protective mercaptan film as it is formed. The presence of non-abrasive copper cleaning ingredients permits the elimination of, or a reduction in,'
copper, as shown in US. Patent 2,628,199, are preferred.
The non-abrasive copper cleaners not only remove oxides from the tarnished copper surface but also permit the simultaneous formation of the continuous transparent fihn of the mercaptan compound. As mentioned earlier, when abrasives alone are employed in conjunction with the mercaptans compounds, the abrading effect tends to remove or disrupt the continuity of the protective film. Although abrasives may desirably be used in addition to the non-abrasive copper cleaners, particularly when heavy sulfide tarnish deposits are encountered, they constitute less than about 20 weight percent of the formulation and are preferably mild abrasives. Among the abrasive materials are finely divided (including m sillcas), clays, d-iatomaceous earths, precipitated chalks, etc.
In addition, sinall quantities of surfactant, particularly the nonionic variety, are usually employed. Viscosity acidic media.
stick or as a paste. Fol-certain uses it may be desirable ta impre griat fabrics with these anti-tarnish compositions to provide a convenient applicator cloth. It is also possible to dispense these compositions from pressurized containers, e.g., aerosols, etc.
Although the mercaptan, or mixture of mereaptans, can be incorporated in varying amounts into the compositions of this invention, depending partly on the physical nature of the formulation, it has been found that mercaptan conoentration within the 0.5 to 25, preferably 0.5 to 10, weight percent range is particularly effective in formations containing a non-abrasive copper cleaner. Less than about 0.5 percent of mercaptan does not generally provide suflicient tarnish resistance.
In an aqueous liquid composition the most preferred formulations usually contain from about 1 to weight percent of mercaptan, 0.01% to 25% of a weak organic f acid, 0.01% to 25% of an alkali metal halide (e.g., alkali metal chlorides, etc.), 0.05% to 1% of a surfactant, 0 to of an abrasive, sufficient water to emulsify the mercaptan, and sutiicient acid stable thickeners to provide the desired viscosity.
The anti-tarnish composition may be applied to the copper-containing surface by spraying, dipping, roll coating, applicator cloth, etc. If an abrasive is included in the formulation, the copper surface is polished until the tarnish deposits are removed. When -no abrasive is used, suflioient contact time is allowed to permit the copper cleaner to loosen and/or remove the tarnish, preferably followed y bufiing or wiping to bring out the lustre of the coppe surface. The removal of all tarnish is essential to obtain the continuous protective film required for extended protection of the surface. In all instances it is usually preferable to rinse the treated surface with water to remove an residual non-abrasive o0 er cleaner and g firasives Ihe following examples Wlll illustrate he various preferred formulations, their use and effectiveness in preventing the tarnishing of copper-containing surfaces for prolonged periods.
Example I Test panels of copper and brass were degreased with trichloroethylene and polished with a commercial copper cleaner containing a non-abrasive copper cleaner, i.e., citric acid and sodium chloride, to remove all traces of tarnish. Immediately after cleaning (a water rinse is preferable), the dry copper-containing surfaces were sprayed with a one percent solution of n-octadecane-lthiol in petroleum ether and buffed with a soft cloth. The panels were then exposed to hydrogen sulfide at about 70% relative humidity along with cleaned uncoated control panels. A marked difference in tarnish rate was noticed, the deposits forming on the controls in less than 15 minutes and the coated panels remaining essentially tarnish free for several hours.
Example 11 The procedure of Example I was repeated using nheneicosane-l-thiol instead of n-ocadecane-l-thiol. After exposure to the hydrogen sulfide atmosphere, the control panels (both copper and brass) tarnished in less than 15 minutes, whereas the treated panels were essentially tarnish free for several hours.
4 Example III The following formulation was prepared, the percentages being by weight:
Percent Water 60 Colloidal alumina (AlOOH) 3 n-Octadecane-l-mercaptan l0 Citric acid 8 Sodium chloride 8 Abrasive (50% diatomaceous earth and 50% of 240 mesh silica) 10 Nonionic surfactant 1 The colloidal alumina thickener was dissolved in water and the temperature raised to C. After mixing the mercaptan and the nonion-ic surfactant and heating to 80 C., the mixture was added to the colloidal alumina solution with high speed mixing, forming a thick creamy emulsion. Once emulsification was complete, the citric acid and the abrasive were added with continued stirring until a homogeneous dispersion was obtained. Then upon adding the sodium chloride, immediate thickening to a. smooth viscous paste occurred.
Copper panels were treated with the above formulation using a soft cloth, followed by water rinsing and air drying. Untreated copper panels whch had been cleaned to remove tarnish were used as controls. After immersing both a treated and an untreated panel in a 1% aqueous solution of hydrogen sulfide, the untreated control was observed to tarnish after 5 seconds whereas tarnishing of the treated panel occurred only after about 2 hours. A similar comparative test using a salt bath (5% aqueous sodium chloride) resulted in tarnishing of the untreated control in 30 minutes and no visible tarnishing of the treated panel after two days. Still another comparative test was made by placing both treated and untreated panels in a high temperature (212 F.) oxidative (air) environment, resulting in tarnishing of the untreated control in 10 minutes and tarnishing of the treated panel only after 6 hours. In each of the foregoing comparative tests the time reported is the time required for visible signs of tarnish to appear.
Example IV Results similar to those in Example III are obtained with the following formulation:
Percent Water 76 Hydrochloric acid 2.5 Colloidal alumina 4 Abrasive 15 n-Octadecane-l-mercaptan 2.4 Nonionic surfactant 0.1
Example V Results similar to those in Example III are obtained with the following formulation:
Percent Colloidal alumina 2.5 n-Octadecane-l-mercaptan 2.4 Citric acid 12 Sodium chloride 12 Diatomaceous earth 15 Nonionic surfactant 1 Water 55 Example VI A composition for dip treatment of tarnished copper panels was prepared with the following ingredients:
Tarnished copper panels were immersed in the above formulation, agitation being used to stabilize the dispersion. Tarnish deposits were removed within a few seconds. The panels were then rinsed with water Excellent resistance to tarnishing over an extended period of time was noted.
As used herein, copper is used interchangeably with copper-containing and includes, besides copper, such copper-containing alloys as brass, bronze, etc. having significant quantities of copper therein.
Various other embodiments and modifications will be apparent to those skilled in the art from the foregoing disclosure without departing from the spirit and scope of this invention.
We claim:
1. An aqueous anti-tarnish composition for copper which consists essentially of 0.01% to 25% of a weak organic acid, 0.01% to 25% of an alkali metal halide, 0.05% to 1% of a surfactant, 0 to 20% of abrasive, and 1 to 15% of a mercaptan of the formula where n is an integer from 12 to 25, the pH of said composition being below about 2.5.
References Cited by the Examiner UNITED STATES PATENTS 3/1945 Barnum 1486.24 7/1958 Murphy 1486.24
OTHER REFERENCES Bennett et al., The Chemical Formulary, vol. I, pages 417-32, published by D. Van Nostrand Co., Inc., New York., 1933.
ALEXANDER H. BRODMERKEL, Primary Examiner.
JOSEPH REBOLD, MORRIS LIEBMAN, Examiners.

Claims (1)

1. AN AQEOUS ANTI-TARNISH COMPOSITION FOR COPPER WHICH CONSISTS ESSENTIALLY OF 0.01% TO 25% OF A WEAK ORGANIC ACID, 0.01% TO 25% OF AN ALKALI METAL HALIDE, 0.05% TO 1% OF A SURFACTANT, 0 TO 20% OF ABRASIVE, AND 1 TO 15% OF A MERCAPTAN OF THE FORMULA
US141292A 1961-09-28 1961-09-28 Anti-tarnish composition for coppercontaining surfaces Expired - Lifetime US3248235A (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
BE622957D BE622957A (en) 1961-09-28
NL283747D NL283747A (en) 1961-09-28
US141292A US3248235A (en) 1961-09-28 1961-09-28 Anti-tarnish composition for coppercontaining surfaces
ES280824A ES280824A1 (en) 1961-09-28 1962-09-15 Improvements introduced in the preparation of compositions against binding in copper (Machine-translation by Google Translate, not legally binding)
SE10116/62A SE310529B (en) 1961-09-28 1962-09-20
FR910332A FR1347705A (en) 1961-09-28 1962-09-25 Composition preventing tarnishing of copper-based surfaces
CH1126362A CH418088A (en) 1961-09-28 1962-09-25 Mixture to prevent tarnishing of copper-containing surfaces
DK420562AA DK113660B (en) 1961-09-28 1962-09-27 Method and means for providing an anti-tarnish film on a decorative copper surface or copper-containing surface.
GB36944/62A GB956927A (en) 1961-09-28 1962-09-28 Anti-tarnish composition for copper-containing surfaces

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US141292A US3248235A (en) 1961-09-28 1961-09-28 Anti-tarnish composition for coppercontaining surfaces

Publications (1)

Publication Number Publication Date
US3248235A true US3248235A (en) 1966-04-26

Family

ID=22495046

Family Applications (1)

Application Number Title Priority Date Filing Date
US141292A Expired - Lifetime US3248235A (en) 1961-09-28 1961-09-28 Anti-tarnish composition for coppercontaining surfaces

Country Status (8)

Country Link
US (1) US3248235A (en)
BE (1) BE622957A (en)
CH (1) CH418088A (en)
DK (1) DK113660B (en)
ES (1) ES280824A1 (en)
GB (1) GB956927A (en)
NL (1) NL283747A (en)
SE (1) SE310529B (en)

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3345295A (en) * 1963-02-13 1967-10-03 Shulton Inc Copper cleaning compositions
US3346405A (en) * 1964-12-14 1967-10-10 Gen Electric Metal protectant
US3385682A (en) * 1965-04-29 1968-05-28 Sprague Electric Co Method and reagent for surface polishing
US3410703A (en) * 1965-05-18 1968-11-12 Hunt Chem Corp Philip A Silver and copper tarnish preventatives
US3442810A (en) * 1966-02-25 1969-05-06 Garman Co Inc Chemical polishing composition and method
US3452503A (en) * 1966-05-10 1969-07-01 North American Rockwell Process and product for confining hydrogen gas
US3458300A (en) * 1966-07-05 1969-07-29 Wyandotte Chemicals Corp Abrasive cleaning compositions
US3491491A (en) * 1968-01-15 1970-01-27 Us Industries Inc Aluminous slurries containing ferric ammonium citrate
US3503883A (en) * 1964-08-19 1970-03-31 Goddard & Sons Ltd J Metal surface protecting preparations
US3518098A (en) * 1963-06-25 1970-06-30 Goddard & Sons Ltd J Metal protecting preparations
US3637508A (en) * 1970-03-06 1972-01-25 William B Willsey Process and composition for dissolving copper oxide
US3652301A (en) * 1969-10-14 1972-03-28 Almeda J Damron Polish composition
US3944491A (en) * 1975-01-20 1976-03-16 Phillips Petroleum Company Lubricants
US4305779A (en) * 1980-05-28 1981-12-15 The United States Of America As Represented By The United States Department Of Energy Method of polishing nickel-base alloys and stainless steels
US4755223A (en) * 1986-08-22 1988-07-05 Antonio Castaldo Liquid composition for cleaning and polishing cymbals comprising kaolin clay
US4853000A (en) * 1987-11-25 1989-08-01 Potter John L Process and composition for a metal polish
WO2005095675A1 (en) * 2004-03-30 2005-10-13 Middlesex Silver Co. Limited Water-based metal treatment composition
US20090068119A1 (en) * 2005-10-14 2009-03-12 Lee Cawthorne Sprayable Depilatory Composition and a Method of use
EP2278593A4 (en) * 2008-04-30 2013-08-28 Hitachi Chemical Co Ltd CONNECTING MATERIAL AND SEMICONDUCTOR DEVICE
US20230323159A1 (en) * 2020-12-03 2023-10-12 Beijing Huaxia Feiyi Xiangyang The Cultural Industry Co., Ltd Noble metal surface cleaning paste, and preparation method therefor and application thereof

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4100096A (en) 1976-06-04 1978-07-11 Addressograph Multigraph Corp. Cleaner for hydrophilic metal surfaces of lithographic duplicators
NL8301070A (en) * 1983-03-28 1984-10-16 Philips Nv DIE AND METHOD FOR THE MANUFACTURE OF PLASTIC ARTICLES BY APPLICATION OF THE DIE.
US4640713A (en) * 1984-11-19 1987-02-03 S. C. Johnson & Son, Inc. Tarnish remover/metal polish formulation comprising a metal iodide, an acid, and water
US20120189485A1 (en) * 2011-01-21 2012-07-26 Ppg Idustries Ohio, I Nc. Methods of removing rust from a ferrous metal-containing surface
US8852357B2 (en) 2011-09-30 2014-10-07 Ppg Industries Ohio, Inc Rheology modified pretreatment compositions and associated methods of use

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2371143A (en) * 1945-03-13 Corrosion protection of metals
US2841501A (en) * 1957-04-17 1958-07-01 James G Murphy Silver polish

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2371143A (en) * 1945-03-13 Corrosion protection of metals
US2841501A (en) * 1957-04-17 1958-07-01 James G Murphy Silver polish

Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3345295A (en) * 1963-02-13 1967-10-03 Shulton Inc Copper cleaning compositions
US3518098A (en) * 1963-06-25 1970-06-30 Goddard & Sons Ltd J Metal protecting preparations
US3503883A (en) * 1964-08-19 1970-03-31 Goddard & Sons Ltd J Metal surface protecting preparations
US3346405A (en) * 1964-12-14 1967-10-10 Gen Electric Metal protectant
US3385682A (en) * 1965-04-29 1968-05-28 Sprague Electric Co Method and reagent for surface polishing
US3410703A (en) * 1965-05-18 1968-11-12 Hunt Chem Corp Philip A Silver and copper tarnish preventatives
US3442810A (en) * 1966-02-25 1969-05-06 Garman Co Inc Chemical polishing composition and method
US3452503A (en) * 1966-05-10 1969-07-01 North American Rockwell Process and product for confining hydrogen gas
US3458300A (en) * 1966-07-05 1969-07-29 Wyandotte Chemicals Corp Abrasive cleaning compositions
US3491491A (en) * 1968-01-15 1970-01-27 Us Industries Inc Aluminous slurries containing ferric ammonium citrate
US3652301A (en) * 1969-10-14 1972-03-28 Almeda J Damron Polish composition
US3637508A (en) * 1970-03-06 1972-01-25 William B Willsey Process and composition for dissolving copper oxide
US3944491A (en) * 1975-01-20 1976-03-16 Phillips Petroleum Company Lubricants
US4305779A (en) * 1980-05-28 1981-12-15 The United States Of America As Represented By The United States Department Of Energy Method of polishing nickel-base alloys and stainless steels
US4755223A (en) * 1986-08-22 1988-07-05 Antonio Castaldo Liquid composition for cleaning and polishing cymbals comprising kaolin clay
US4853000A (en) * 1987-11-25 1989-08-01 Potter John L Process and composition for a metal polish
WO2005095675A1 (en) * 2004-03-30 2005-10-13 Middlesex Silver Co. Limited Water-based metal treatment composition
US20070277906A1 (en) * 2004-03-30 2007-12-06 Middlesex Silver Co., Limited Water-Based Metal Treatment Composition
US20090068119A1 (en) * 2005-10-14 2009-03-12 Lee Cawthorne Sprayable Depilatory Composition and a Method of use
US9358196B2 (en) * 2005-10-14 2016-06-07 Reckitt Benckiser (Uk) Limited Sprayable depilatory composition and a method of use
EP2278593A4 (en) * 2008-04-30 2013-08-28 Hitachi Chemical Co Ltd CONNECTING MATERIAL AND SEMICONDUCTOR DEVICE
US20230323159A1 (en) * 2020-12-03 2023-10-12 Beijing Huaxia Feiyi Xiangyang The Cultural Industry Co., Ltd Noble metal surface cleaning paste, and preparation method therefor and application thereof

Also Published As

Publication number Publication date
CH418088A (en) 1966-07-31
BE622957A (en)
GB956927A (en) 1964-04-29
ES280824A1 (en) 1963-03-01
NL283747A (en)
SE310529B (en) 1969-05-05
DK113660B (en) 1969-04-14

Similar Documents

Publication Publication Date Title
US3248235A (en) Anti-tarnish composition for coppercontaining surfaces
AU653567B2 (en) Method for cleaning aluminum and aluminum alloys
US3598741A (en) Acid compound for metal surface
CN1089378C (en) Composition for cleaning silver or copper
US4970014A (en) Aluminum cleaning and brightening composition and method of manufacture thereof
US3653095A (en) Synergistic combination for inhibiting the attack of alkaline solutions on alkali sensitive substrates
US2689808A (en) Metal plating
US4931102A (en) Metal cleaning process
US2220451A (en) Composition
US2841501A (en) Silver polish
US5215676A (en) Rust and stain removal composition
US3510432A (en) Noncorrosive rust remover
US5614028A (en) Method of cleaning and passivating a metal surface with acidic system and ethoxylated tertiary dodecyl mercaptan
US5019288A (en) Cleaning composition for copper and copper alloys and method of manufacture thereof
NO130387B (en)
US3173875A (en) Acid bowl cleaner
US3653931A (en) Anti-tarnish composition for metal surfaces and process for its use
US3365312A (en) Metal cleaner, article and method
US3398003A (en) Silver polish-tarnish retarder containing a dialkyl disulfide having from 8 to 20 carbon atoms in each alkyl radical
US4925491A (en) Solutions and creams for silver plating and polishing
EP0182368A2 (en) Tarnish remover/metal polish formulation comprising a metal iodide, an acid and water
US3117012A (en) Silver polish
US5534177A (en) Compositions useful for removing products of metal corrosion
US3649373A (en) Passivating agent for protecting the surfaces of silver-bearing materials
US4561895A (en) Non-abrasive metal cleaning agent