[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

US3412032A - Etching bath composition - Google Patents

Etching bath composition Download PDF

Info

Publication number
US3412032A
US3412032A US429635A US42963565A US3412032A US 3412032 A US3412032 A US 3412032A US 429635 A US429635 A US 429635A US 42963565 A US42963565 A US 42963565A US 3412032 A US3412032 A US 3412032A
Authority
US
United States
Prior art keywords
etching
etching bath
metal
acid
aqueous
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
US429635A
Inventor
Richard H Jenks
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.)
Revere Copper and Brass Inc
Original Assignee
Revere Copper and Brass Inc
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
Application filed by Revere Copper and Brass Inc filed Critical Revere Copper and Brass Inc
Priority to US429635A priority Critical patent/US3412032A/en
Application granted granted Critical
Publication of US3412032A publication Critical patent/US3412032A/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
    • 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
    • C23F1/00Etching metallic material by chemical means
    • C23F1/10Etching compositions
    • C23F1/14Aqueous compositions
    • C23F1/16Acidic compositions

Definitions

  • This invention relates to the etching of metal and, more particularly, to a novel etching bath composition capable of effecting controlled etching of metal surfaces.
  • Controlled etching of a metal surface is required in a number of arts.
  • the surface is covered with a light-sensitive coating, the coating is exposed to light through a negative of the desired image, and then the exposed surface is heated to develop the image on the metal surf-ace in the form of an acid-insoluble residue called the resist.
  • the resist-bearing metal surface is bathed by splashing over it a corrosive acid mixture of proper composition, the corrosion of the metal not pro tected by the resist can be controlled so as not to undercut the metal lying under the resist.
  • a similar type of controlled etching is required in the production of printed electronic circuits and chemical milling.
  • Controlled etching bath com-positions are described in United States Patents Nos. 2,640,763, 2,640,764, 2,640,- 765, 2,640,766, 2,640,767, 2,763,536, 2,828,194, 2,940,- 836, 2,979,387 and 3,023,138.
  • the effectiveness of the baths described in all of these patents is based upon the use of nitric acid as the corrosive medium.
  • the novel etching bath of the present invention comprises a mixture of an aqueous solution of sulfuric acid and hydrogen peroxide with an organic corrosion inhibitor.
  • the sulfuric acid content of the aqueous corrosion medium of the new etching bath is effective within the range of about 4% to about 20% by volume of H 50 Within this range, the optimum acid concentration varies with the metal to be etched. For example, in etching zinc an acid concentration of about 5 to 7% is particularly satisfactory, and for etching copper an acid concentration of about 8 to 12% is presently preferred.
  • the sulfuric acid need not, of course, be added as 100% acid but can be used in any concentration capable, considering the water content of the added hydrogen peroxide component, of establishing the H SO content within the aforementioned prescription.
  • the hydrogen peroxide content of the aqueous corrosion medium is effective within a range of about 4% to about 15% by volume of H 0 Within this range the optimum concentration varies with the metal being etched and can be readily determined by simple testing. For example, in etching zinc, concentrations of about 5% to about 8% are particularly satisfactory, and a concentration of about 5 to 6% is presently preferred.
  • the hydrogen peroxide is advantageously added in the form of a 50% aqueous solution, but other concentrations of the hydrogen peroxide component can be used provided that they are sufficiently high to permit the formation of an aqueous corrosion medium containing both the sulfuric acid and the hydrogen peroxide within the recited ranges of concentrations.
  • the inhibitor can be (-a) a saturated aliphatic monobasic or poly'basic acid or its metal salt, advantageously limited to those containing 5 to 26 carbon atoms, in which at least one carboxylic group is present, such, for example, as oleic and stearic acids, metal oleates and stearates, etc., (b) an ester of such an aliphatic acid and a polyhydric aliphatic alcohol, (c) an ester of sulfosuccinic acid and an aliphatic alcohol, (d) a petroleum sulfonate such as a petroleum sulfonic acid or a mahogany soap, (e) a Water-soluble anionic surface-active agent containing a sulfate radical with at least about 8% s
  • the amount of organic corrosion inhibitor useful in practicing the invention generally does not exceed about 1.5% by weight of the aqueous sulfuric acid-hydrogen peroxide solution and at present is used in amounts less than about 1% but not less than about 0.1% by weight of the aqueous corrosion medium.
  • the optimum specific amount of any such organic corrosion inhibitor used in the practice of the invention depends upon the concentration of the sulfuric acid and hydrogen peroxide components of the aqueous corrosion medium, the temperature of this medium used in the etching operation, the composition of the metal being etched, and the design of the vessel and etchant-splashing device used for the etching operation.
  • the inhibitor action can be modified by further addition to the etching bath of a water-insoluble organic liquid such as kerosene, gasoline, benzene, coal oil and lubricating oils, in amounts ranging from about 0.1 to about 10% by volume of the aqueous corrosion medium, and the presence of such an organic liquid in the etching bath will also affect the optimum amount of organic corrosion inhibitor.
  • a water-insoluble organic liquid such as kerosene, gasoline, benzene, coal oil and lubricating oils
  • etching bath compositions of the present invention are useful in effecting controlled etching of such metals as zinc, copper, magnesium, nickel and iron, as well as alloys based on these metals.
  • EXAMPLE A zinc-base alloy of the type used for commercial photoengraving was conventionally exposed and developed by etching in a standard photoengraving etching machine.
  • the aqueous etching bath having a total volume of 78 liters, was prepared by adding to the water component 6% by volume of C.P. H SO 5% by volume of H 0 (added as 10% by volume of a 50% aqueous solution of H 0 0.27% of sulfonated castor oil (American Cyanamids AR), 0.047% of a petroleum sulfonate having a molecular weight range of about 200-600, and 0.013% of commercial grade oleic acid.
  • the plate was etched in this bath in the machine for 20 minutes, following which the plate was washed and dried.
  • the etched plate showed controlled etching of the metal with lines and half-tones representative of the image being reproduced.
  • a metal controlled-etching bath consisting essentially of an aqueous solution containing by volume about 5 to 7% H 80 and about 5 to 6% H 0 said solution further containing about 0.1 to 1% by weight of an organic corrosion inhibitor.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • ing And Chemical Polishing (AREA)

Description

United States Patent 3,412,032 ETCHING BATH COMPOSITION Richard H. Jenks, Sauquoit, N.Y., assignor to Revere Copper and Brass Incorporated, Rome, N.Y., a corporation of Maryland No Drawing. Filed Feb. 1, 1965, Ser. No. 429,635 1 Claim. (Cl. 25279.4)
This invention relates to the etching of metal and, more particularly, to a novel etching bath composition capable of effecting controlled etching of metal surfaces.
Controlled etching of a metal surface is required in a number of arts. For example, in the production of photoengraving metal printing surfaces, the surface is covered with a light-sensitive coating, the coating is exposed to light through a negative of the desired image, and then the exposed surface is heated to develop the image on the metal surf-ace in the form of an acid-insoluble residue called the resist. If the resist-bearing metal surface is bathed by splashing over it a corrosive acid mixture of proper composition, the corrosion of the metal not pro tected by the resist can be controlled so as not to undercut the metal lying under the resist. A similar type of controlled etching is required in the production of printed electronic circuits and chemical milling.
Controlled etching bath com-positions are described in United States Patents Nos. 2,640,763, 2,640,764, 2,640,- 765, 2,640,766, 2,640,767, 2,763,536, 2,828,194, 2,940,- 836, 2,979,387 and 3,023,138. The effectiveness of the baths described in all of these patents is based upon the use of nitric acid as the corrosive medium. I have now discovered that an aqueous mixture of sulfuric acid and hydrogen peroxide can be substituted for the aqueous nitric acid solution in each of the aforementioned patents and that the corrosion inhibitors described in those patents are effective, in combination with an aqueous sulfuric acid-hydrogen peroxide solution, in forming an etching bath capable of controlled etching of the surface of zinc, magnesium, copper, nickel and iron, and alloys based On these metals, for producing photoengraving and printed circuit sheets, and the like. Thus, the novel etching bath of the present invention comprises a mixture of an aqueous solution of sulfuric acid and hydrogen peroxide with an organic corrosion inhibitor.
The sulfuric acid content of the aqueous corrosion medium of the new etching bath is effective within the range of about 4% to about 20% by volume of H 50 Within this range, the optimum acid concentration varies with the metal to be etched. For example, in etching zinc an acid concentration of about 5 to 7% is particularly satisfactory, and for etching copper an acid concentration of about 8 to 12% is presently preferred. The sulfuric acid need not, of course, be added as 100% acid but can be used in any concentration capable, considering the water content of the added hydrogen peroxide component, of establishing the H SO content within the aforementioned prescription.
The hydrogen peroxide content of the aqueous corrosion medium is effective within a range of about 4% to about 15% by volume of H 0 Within this range the optimum concentration varies with the metal being etched and can be readily determined by simple testing. For example, in etching zinc, concentrations of about 5% to about 8% are particularly satisfactory, and a concentration of about 5 to 6% is presently preferred. The hydrogen peroxide is advantageously added in the form of a 50% aqueous solution, but other concentrations of the hydrogen peroxide component can be used provided that they are sufficiently high to permit the formation of an aqueous corrosion medium containing both the sulfuric acid and the hydrogen peroxide within the recited ranges of concentrations.
To the aqueous corrosion medium consisting essentially of the sulfuric acid and hydrogen peroxide solution, there is admixed an organic corrosion inhibitor such as any of those referred to in the aforementioned patents. Thus, the inhibitor can be (-a) a saturated aliphatic monobasic or poly'basic acid or its metal salt, advantageously limited to those containing 5 to 26 carbon atoms, in which at least one carboxylic group is present, such, for example, as oleic and stearic acids, metal oleates and stearates, etc., (b) an ester of such an aliphatic acid and a polyhydric aliphatic alcohol, (c) an ester of sulfosuccinic acid and an aliphatic alcohol, (d) a petroleum sulfonate such as a petroleum sulfonic acid or a mahogany soap, (e) a Water-soluble anionic surface-active agent containing a sulfate radical with at least about 8% sulfation such, for example, as sulfated tall oil, sulfated castor oil, etc., (f) alkylarylsulfonates such as alkylbenzene and alkylnaphthalene sulfonates in which the alkyl group contains 8 to 18 carbon atoms, and (g) halogenated diaryloxide sulfonic acids and their salts, such as those described in United States Patent No. 2,081,876.
The amount of organic corrosion inhibitor useful in practicing the invention generally does not exceed about 1.5% by weight of the aqueous sulfuric acid-hydrogen peroxide solution and at present is used in amounts less than about 1% but not less than about 0.1% by weight of the aqueous corrosion medium. The optimum specific amount of any such organic corrosion inhibitor used in the practice of the invention depends upon the concentration of the sulfuric acid and hydrogen peroxide components of the aqueous corrosion medium, the temperature of this medium used in the etching operation, the composition of the metal being etched, and the design of the vessel and etchant-splashing device used for the etching operation. Moreover, the inhibitor action can be modified by further addition to the etching bath of a water-insoluble organic liquid such as kerosene, gasoline, benzene, coal oil and lubricating oils, in amounts ranging from about 0.1 to about 10% by volume of the aqueous corrosion medium, and the presence of such an organic liquid in the etching bath will also affect the optimum amount of organic corrosion inhibitor.
The etching bath compositions of the present invention are useful in effecting controlled etching of such metals as zinc, copper, magnesium, nickel and iron, as well as alloys based on these metals.
The following example is illustrative of the practice of the invention:
EXAMPLE A zinc-base alloy of the type used for commercial photoengraving was conventionally exposed and developed by etching in a standard photoengraving etching machine. The aqueous etching bath, having a total volume of 78 liters, was prepared by adding to the water component 6% by volume of C.P. H SO 5% by volume of H 0 (added as 10% by volume of a 50% aqueous solution of H 0 0.27% of sulfonated castor oil (American Cyanamids AR), 0.047% of a petroleum sulfonate having a molecular weight range of about 200-600, and 0.013% of commercial grade oleic acid. The plate was etched in this bath in the machine for 20 minutes, following which the plate was washed and dried. The etched plate showed controlled etching of the metal with lines and half-tones representative of the image being reproduced.
I claim:
1. A metal controlled-etching bath consisting essentially of an aqueous solution containing by volume about 5 to 7% H 80 and about 5 to 6% H 0 said solution further containing about 0.1 to 1% by weight of an organic corrosion inhibitor.
References Cited UNITED STATES PATENTS Hull 25279.2 X Kepfer 252-79.2 X Hopkins et al. 252151 X Margulies 252-79.2X Le Boucher 252-395 MAYER WEINBLATI, Primary Examiner.

Claims (1)

1. A METAL CONTROLLED-ETCHING BATH CONSISTING ESSENTIALLY OF AN AQUEOUS SOLUTION CONTAINING BY VOLUME ABOUT 5 TO 7% H2SO4 AND ABOUT 5 TO 6% H2O2, SAID SOLUTION FURTHER CONTAINING ABOUT 0.1 TO 1% BY WEIGHT OF AN ORGANIC CORROSIN INHIBITOR.
US429635A 1965-02-01 1965-02-01 Etching bath composition Expired - Lifetime US3412032A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US429635A US3412032A (en) 1965-02-01 1965-02-01 Etching bath composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US429635A US3412032A (en) 1965-02-01 1965-02-01 Etching bath composition

Publications (1)

Publication Number Publication Date
US3412032A true US3412032A (en) 1968-11-19

Family

ID=23704094

Family Applications (1)

Application Number Title Priority Date Filing Date
US429635A Expired - Lifetime US3412032A (en) 1965-02-01 1965-02-01 Etching bath composition

Country Status (1)

Country Link
US (1) US3412032A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2364162A1 (en) * 1972-12-22 1974-07-11 Furukawa Electric Co Ltd ACID AQUATIC SOLUTION FOR TREATMENT OF METALS
US3931030A (en) * 1973-10-02 1976-01-06 Kenseido Kagaku Kogyo Kabushiki Kaisha Etching composition for etching nickel screen rolls or plates
US3948703A (en) * 1973-03-27 1976-04-06 Tokai Denka Kogyo Kabushiki Kaisha Method of chemically polishing copper and copper alloy
US4233111A (en) * 1979-06-25 1980-11-11 Dart Industries Inc. Dissolution of metals utilizing an aqueous H2 SO4 -H2 O2 -3-sulfopropyldithiocarbamate etchant
US4233112A (en) * 1979-06-25 1980-11-11 Dart Industries Inc. Dissolution of metals utilizing an aqueous H2 SO4 -H2 O2 -polysulfide etchant
US4233113A (en) * 1979-06-25 1980-11-11 Dart Industries Inc. Dissolution of metals utilizing an aqueous H2 O2 -H2 SO4 -thioamide etchant
US4236957A (en) * 1979-06-25 1980-12-02 Dart Industries Inc. Dissolution of metals utilizing an aqueous H2 SOY --H2 O.sub. -mercapto containing heterocyclic nitrogen etchant
US4904340A (en) * 1988-10-31 1990-02-27 Microelectronics And Computer Technology Corporation Laser-assisted liquid-phase etching of copper conductors
US6310017B1 (en) 1999-02-01 2001-10-30 Ct Associates, Inc. Cleaner composition, method for making and using same

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2154451A (en) * 1934-12-17 1939-04-18 Du Pont Bright dip
US2154455A (en) * 1934-02-08 1939-04-18 Du Pont Cadmium bright dip
US2828194A (en) * 1956-09-28 1958-03-25 Dow Chemical Co Etching
US2923608A (en) * 1956-04-13 1960-02-02 Fmc Corp Method of improving the bonding properties of steel surfaces
US3062612A (en) * 1959-04-25 1962-11-06 Inst Francais Du Petrole Method of protecting metals against electrochemical corrosion of the acidic type

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2154455A (en) * 1934-02-08 1939-04-18 Du Pont Cadmium bright dip
US2154451A (en) * 1934-12-17 1939-04-18 Du Pont Bright dip
US2923608A (en) * 1956-04-13 1960-02-02 Fmc Corp Method of improving the bonding properties of steel surfaces
US2828194A (en) * 1956-09-28 1958-03-25 Dow Chemical Co Etching
US3062612A (en) * 1959-04-25 1962-11-06 Inst Francais Du Petrole Method of protecting metals against electrochemical corrosion of the acidic type

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2364162A1 (en) * 1972-12-22 1974-07-11 Furukawa Electric Co Ltd ACID AQUATIC SOLUTION FOR TREATMENT OF METALS
US3905907A (en) * 1972-12-22 1975-09-16 Furukawa Electric Co Ltd Solutions for chemical dissolution treatment of metal materials
US3948703A (en) * 1973-03-27 1976-04-06 Tokai Denka Kogyo Kabushiki Kaisha Method of chemically polishing copper and copper alloy
US3931030A (en) * 1973-10-02 1976-01-06 Kenseido Kagaku Kogyo Kabushiki Kaisha Etching composition for etching nickel screen rolls or plates
US4233111A (en) * 1979-06-25 1980-11-11 Dart Industries Inc. Dissolution of metals utilizing an aqueous H2 SO4 -H2 O2 -3-sulfopropyldithiocarbamate etchant
US4233112A (en) * 1979-06-25 1980-11-11 Dart Industries Inc. Dissolution of metals utilizing an aqueous H2 SO4 -H2 O2 -polysulfide etchant
US4233113A (en) * 1979-06-25 1980-11-11 Dart Industries Inc. Dissolution of metals utilizing an aqueous H2 O2 -H2 SO4 -thioamide etchant
US4236957A (en) * 1979-06-25 1980-12-02 Dart Industries Inc. Dissolution of metals utilizing an aqueous H2 SOY --H2 O.sub. -mercapto containing heterocyclic nitrogen etchant
US4904340A (en) * 1988-10-31 1990-02-27 Microelectronics And Computer Technology Corporation Laser-assisted liquid-phase etching of copper conductors
US6310017B1 (en) 1999-02-01 2001-10-30 Ct Associates, Inc. Cleaner composition, method for making and using same

Similar Documents

Publication Publication Date Title
US3668131A (en) Dissolution of metal with acidified hydrogen peroxide solutions
US3412032A (en) Etching bath composition
US4705665A (en) Method for inhibiting oxidation of ferrous metals with alkyl glycosides and composition for cleaning ferrous metals
US4004956A (en) Selectively stripping tin or tin-lead alloys from copper substrates
EP0183775B1 (en) Selective nickel stripping compositions and method of stripping
US3407141A (en) Dissolution of metal with acidified hydrogen peroxide solutions
GB865192A (en) Improvements in or relating to corrosion inhibitors
US2979387A (en) Etching
US2828194A (en) Etching
AU612305B2 (en) Hydrogen peroxide compositions containing a substituted aminobenzaldehyde
US4256602A (en) Fluoroborate complex composition and method for cleaning aluminum at low temperatures
US2846295A (en) Etching bath
US3023138A (en) Powderless etching bath and method of etching plates therewith
US3761331A (en) Bath and method for etching aluminum
US2314818A (en) Surface treatment of tinned material
US2692188A (en) Acid pickling compositions and method of pickling
US3689417A (en) Powderless etching bath
US3197340A (en) Composition and method for cleaning aluminum castings
US2154469A (en) Bright dip
US3736197A (en) Powderless etching bath compositions and additives
US3251777A (en) Powderless etching bath
Ammar et al. The anodic behaviour and Passivity of Tin in sulphate solutions
US3656886A (en) Corrosion inhibitors
US3362911A (en) Chromic acid-sulfuric acid solutions containing chloride catalyst for dissolving metals
US3402083A (en) Powderless etching method for etching relief images in aluminum