US3425946A - Electroless plating composition - Google Patents
Electroless plating composition Download PDFInfo
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- US3425946A US3425946A US594952A US3425946DA US3425946A US 3425946 A US3425946 A US 3425946A US 594952 A US594952 A US 594952A US 3425946D A US3425946D A US 3425946DA US 3425946 A US3425946 A US 3425946A
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- United States
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- solution
- base
- plastic
- stannous chloride
- electroless plating
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- Expired - Lifetime
Links
- 238000007772 electroless plating Methods 0.000 title description 5
- 239000000203 mixture Substances 0.000 title description 3
- 239000000243 solution Substances 0.000 description 28
- 238000000034 method Methods 0.000 description 21
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 18
- 239000004033 plastic Substances 0.000 description 18
- 229920003023 plastic Polymers 0.000 description 18
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 12
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 12
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 12
- 239000001119 stannous chloride Substances 0.000 description 12
- 235000011150 stannous chloride Nutrition 0.000 description 12
- -1 copper and nickel Chemical class 0.000 description 10
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical class CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 8
- 229910052802 copper Inorganic materials 0.000 description 8
- 239000010949 copper Substances 0.000 description 8
- 238000005530 etching Methods 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 230000003750 conditioning effect Effects 0.000 description 4
- 230000008021 deposition Effects 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 238000007747 plating Methods 0.000 description 4
- 235000013772 propylene glycol Nutrition 0.000 description 4
- 230000001235 sensitizing effect Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000005215 alkyl ethers Chemical class 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 150000001879 copper Chemical class 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical class [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- AOPDRZXCEAKHHW-UHFFFAOYSA-N 1-pentoxypentane Chemical class CCCCCOCCCCC AOPDRZXCEAKHHW-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 235000001543 Corylus americana Nutrition 0.000 description 1
- 240000007582 Corylus avellana Species 0.000 description 1
- 235000007466 Corylus avellana Nutrition 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 150000001983 dialkylethers Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical class [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Chemical class 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical class [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000011006 sodium potassium tartrate Nutrition 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- CVNKFOIOZXAFBO-UHFFFAOYSA-J tin(4+);tetrahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[Sn+4] CVNKFOIOZXAFBO-UHFFFAOYSA-J 0.000 description 1
- QHGNHLZPVBIIPX-UHFFFAOYSA-N tin(ii) oxide Chemical class [Sn]=O QHGNHLZPVBIIPX-UHFFFAOYSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
- C23C18/18—Pretreatment of the material to be coated
- C23C18/20—Pretreatment of the material to be coated of organic surfaces, e.g. resins
- C23C18/22—Roughening, e.g. by etching
- C23C18/26—Roughening, e.g. by etching using organic liquids
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
- C23C18/18—Pretreatment of the material to be coated
- C23C18/20—Pretreatment of the material to be coated of organic surfaces, e.g. resins
- C23C18/28—Sensitising or activating
- C23C18/285—Sensitising or activating with tin based compound or composition
Definitions
- the present invention is directed to plating of metals, such as copper and nickel, on non-conducting bases, and more particularly to electroless deposition of the metal.
- Procedures of this kind have been in use for a considerable time. They treated the plastic base to clean the surface, then sensitized the base which was then treated with a palladium chloride solution which was a catalyst or activator, after which the copper salt solution was applied to form the plating.
- etching and conditioning solutions are highly acidic solutions that chemically alter the surface of the plastic without overly marring or breaking down its molecular structure. Unlike etching, conditioning does not roughen the surface.
- One process employs an acid dip conditioner followed by sensitizing and activating solutions which prepare the surface for an electroless copper deposit.
- the sensitizer normally used is an acidified solution of stannous chloride.
- the other process uses an intermediate step following the etching treatment. This step forms a thin, water-soluble film of resin on the surface of the plastic. This resin is not crosslinked at this point, so as to allow the absorption of a sensitizing metal from solution in a later step. Following this step, the resin film is crosslinked and the surface prepared catalytically for the deposition of electroless copper in a pre-plate solution.
- the present invention is intended and adapted to eliminates the difiiculties and disadvantages inherent in prior processes and to provide a one-step process thereby eliminating the necessity of a three-step process (precleaning, etching and sensitizing), as heretofore described, for the preparation and conditioning of substrate prior to the deposition of electroless plating.
- the invention is based on the discovery that a glycol ether solvent has all the properties necessary to properly prepare the surface of a plastic body so as to hold the copper plate firmly in position. Most solvents leave the surface of a plastic, such as an acrylic resin, hydrophobic or do not attack the surface at all or do not wet the surface.
- glycol ethers such as the alkyl ethers of ethylene or propylene glycols and the dialkyl ethers of such glycols attack the surface of an acrylic resin, and are sufficiently soluble in water so that they rinse off the work readily. As such these solvents are readily removable and are not adsorbed onto the resin. In addition, they have a mild etching action on the base.
- glycol ethers When such glycol ethers are used alone to condition the surface it is found that the eventual plate is apt not to be even and it is sometimes difiicult to control the action thereof on the base. It has been found that stannous chloride is soluble in these glycol ethers and also that such a solution when applied to the base conditions the surface, sensitizes it and cleans off any film of oil or other substances on the surface due to handling. The effect of the solution is definite and readily controllable. Therefore, such a solution is preferred for the operation.
- the three steps previously employed are combined into one step.
- the use of this one step method increases the adhesion properties on the surface of the plastic making the metalto-plastic bond stronger and more readily acceptable to subsequent deposits of electroless copper.
- the plastic is cleaned, etched and swollen to expose the pores, made hydrophilic, and sensitized in one bath. On subsequent rinsing and the rise in pH, the
- stannous chloride is preciptated as the oxide or hydroxide, and excess solvent is readily leached from the plastic, reducing the swelling and firmly bonding the sensitizer to the plastic mechanically as well as the chemical bonds which are present.
- the glycol ethers used may be of the ethylene glycol ether (Cellosolve) or diethylene glycol ether (Carbitol) family, methyl to the butyl or amyl ethers being most readily available.
- Other glycol ethers such as propylene glycol ethers may also be used.
- the said glycol ethers are those in which the alkyl radicals have from 1 to 5 carbon atoms.
- the stannous chloride content may be as low as .1% up to the saturation point, although above 5% the bulk of the stannous chloride is rinsed from the work.
- Other sensitizers such as titanous chloride may be treated in a like manner.
- the time of treatment wth the stannous chloride-glycol solution may vary considerably. A treatment for about one minute will result in a bright copper deposit because of the extreme thinness of the deposit, since it has a smoother surface. Such deposits are useful primarily for decorative articles not subject to wear or abrasion.
- the treatment may be as long as ten or more minutes of etching time resulting in good adhesion of the plating on the plastic base, making an article which is quite resistant to abrasion. It has been found that etching for about 5 to 8 minutes gives highly satisfactory results. The operation is conducted at approximately room temperature.
- auxiliary solvent such as monohydric alcohols, esters of low carbon acids, ketones, halogenated hydrocarbons, such as chlorinated solvents, said compounds having 1 to 8 carbon atoms, and acid activators which are advantageous where titanium dioxide filler is present, to increase the etch or swell or plastic.
- acids include the lower aliphatic acids, such as chloracetic, butyric and others, even inorganic acids.
- the stannous chloride-glycol solution in hydrochloric acid is placed in contact with the acrylic base for say 5 minutes. Then the base is rinsed with water to remove the acid, whereby the pH rises and the stannous chloride breaks down to stannous hydroxide or oxide, being held on the surface of the base. The water becomes cloudy during the operation. Then, as in the prior art a 1% solution in water of palladium chloride in hydrochloric acid is applied to the base; it reacts with the stannous compound and is transformed to a colloidal form of palladium which becomes firmly keyed to the etched irregularities of the base.
- a solution of a copper salt such as copper sulfate, containing sodium hydroxide and Rochelle salts and formaldehyde, forming a smooth, non-porous, highly adherent deposit.
- the essence of the invention lies in the preliminary treatment of the base, which may be other resins or plastic non-conducting materials than acrylic resins.
- This treatment is by a substantially water-free solution of the stannous chloride in the glycols described herein. It eliminates the necessity for such pretreatments of the base as degreasing, abrading, cleaning, etc. It combines three steps of the prior art into one step and avoids the necessity of heating in the operation.
- a method of treating a substantially non-conducting plastic base for electroless plating of a metal thereon which comprises preparing a solution consisting essentially of a reducible stannous compound in a glycol ether selected from the class consisting of the alkyl ethers of ethylene glycol, diethylene glycol, and propylene glycol wherein the alkyl radicals have from 1 to 5 carbon atoms, and contacting said base with said solution for a sufficient time to etch the surface of said base, and then washing said treated base to remove excess of said solution.
- a composition for treating a substantially nonconducting plastic base for electroless plating consisting essentially of a solution in a glycol ether selected from the class consisting of the alkyl ethers of ethylene glycol, diethylene glycol, and propylene glycol wherein the alkyl radicals have from 1 to 5 carbon atoms of about 0.1% to saturation of stannous chloride.
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- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemically Coating (AREA)
Description
United States Patent 3,425,946 ELECTROLESS PLATING COMPOSITION William M. Emons, Jr., Hazel Drive, Branford, Conn. 06405, and Saul Charms, 300 Calvin St., Westwood,
NJ. 07675 No Drawing. Filed Aug. 26, 1966, Ser. No. 594,952 US. Cl. 252-79.1 Claims Int. Cl. C09k 3/00 ABSTRACT OF THE DISCLOSURE The present invention is directed to plating of metals, such as copper and nickel, on non-conducting bases, and more particularly to electroless deposition of the metal.
Procedures of this kind have been in use for a considerable time. They treated the plastic base to clean the surface, then sensitized the base which was then treated with a palladium chloride solution which was a catalyst or activator, after which the copper salt solution was applied to form the plating.
Two techniques for preparing the surface of plastic prior to electroless copper deposition had been developed employing either etching or conditioning solutions in a special bath. Both etching and conditioning solutions are highly acidic solutions that chemically alter the surface of the plastic without overly marring or breaking down its molecular structure. Unlike etching, conditioning does not roughen the surface. One process employs an acid dip conditioner followed by sensitizing and activating solutions which prepare the surface for an electroless copper deposit.
The sensitizer normally used is an acidified solution of stannous chloride. The other process uses an intermediate step following the etching treatment. This step forms a thin, water-soluble film of resin on the surface of the plastic. This resin is not crosslinked at this point, so as to allow the absorption of a sensitizing metal from solution in a later step. Following this step, the resin film is crosslinked and the surface prepared catalytically for the deposition of electroless copper in a pre-plate solution.
Such processes required a series of steps of treatment of the surface of the base with intermediate revising after each step. This introduced the necessity for a substantial amount of equipment and considerable amount of labor for the operations. One of the prior processes involved the application of a chromate chemical etchant, which had a number of disadvantages in that considerable time was necessary for the treatment, the chemicals were corrosive and poisonous creating a hazard for the workmen, and elevated temperatures were necessary in carrying out the treatment, as well as disposal problems of spent solutions.
The present invention is intended and adapted to eliminates the difiiculties and disadvantages inherent in prior processes and to provide a one-step process thereby eliminating the necessity of a three-step process (precleaning, etching and sensitizing), as heretofore described, for the preparation and conditioning of substrate prior to the deposition of electroless plating.
The invention is based on the discovery that a glycol ether solvent has all the properties necessary to properly prepare the surface of a plastic body so as to hold the copper plate firmly in position. Most solvents leave the surface of a plastic, such as an acrylic resin, hydrophobic or do not attack the surface at all or do not wet the surface. On the other hand glycol ethers such as the alkyl ethers of ethylene or propylene glycols and the dialkyl ethers of such glycols attack the surface of an acrylic resin, and are sufficiently soluble in water so that they rinse off the work readily. As such these solvents are readily removable and are not adsorbed onto the resin. In addition, they have a mild etching action on the base.
When such glycol ethers are used alone to condition the surface it is found that the eventual plate is apt not to be even and it is sometimes difiicult to control the action thereof on the base. It has been found that stannous chloride is soluble in these glycol ethers and also that such a solution when applied to the base conditions the surface, sensitizes it and cleans off any film of oil or other substances on the surface due to handling. The effect of the solution is definite and readily controllable. Therefore, such a solution is preferred for the operation.
By the use of stannous chloride dissolved in a glycol ether, soluble or partially soluble in water, the three steps previously employed are combined into one step. The use of this one step method increases the adhesion properties on the surface of the plastic making the metalto-plastic bond stronger and more readily acceptable to subsequent deposits of electroless copper. By the use of this disclosure the plastic is cleaned, etched and swollen to expose the pores, made hydrophilic, and sensitized in one bath. On subsequent rinsing and the rise in pH, the
stannous chloride is preciptated as the oxide or hydroxide, and excess solvent is readily leached from the plastic, reducing the swelling and firmly bonding the sensitizer to the plastic mechanically as well as the chemical bonds which are present.
The glycol ethers used may be of the ethylene glycol ether (Cellosolve) or diethylene glycol ether (Carbitol) family, methyl to the butyl or amyl ethers being most readily available. Other glycol ethers such as propylene glycol ethers may also be used. The said glycol ethers are those in which the alkyl radicals have from 1 to 5 carbon atoms. The stannous chloride content may be as low as .1% up to the saturation point, although above 5% the bulk of the stannous chloride is rinsed from the work. Other sensitizers such as titanous chloride may be treated in a like manner.
The time of treatment wth the stannous chloride-glycol solution may vary considerably. A treatment for about one minute will result in a bright copper deposit because of the extreme thinness of the deposit, since it has a smoother surface. Such deposits are useful primarily for decorative articles not subject to wear or abrasion. The treatment may be as long as ten or more minutes of etching time resulting in good adhesion of the plating on the plastic base, making an article which is quite resistant to abrasion. It has been found that etching for about 5 to 8 minutes gives highly satisfactory results. The operation is conducted at approximately room temperature.
The following specific example is given as a suitable bath for acrylonitrile-butadiene-styrene plastic (A.B.S.):
Composition- Percent by weight Cellosolve (ethylene glycol ether) 99 Stannous chloride 2H O 1 Various other plastics may require an auxiliary solvent such as monohydric alcohols, esters of low carbon acids, ketones, halogenated hydrocarbons, such as chlorinated solvents, said compounds having 1 to 8 carbon atoms, and acid activators which are advantageous where titanium dioxide filler is present, to increase the etch or swell or plastic. Among such acids are the lower aliphatic acids, such as chloracetic, butyric and others, even inorganic acids.
The stannous chloride-glycol solution in hydrochloric acid is placed in contact with the acrylic base for say 5 minutes. Then the base is rinsed with water to remove the acid, whereby the pH rises and the stannous chloride breaks down to stannous hydroxide or oxide, being held on the surface of the base. The water becomes cloudy during the operation. Then, as in the prior art a 1% solution in water of palladium chloride in hydrochloric acid is applied to the base; it reacts with the stannous compound and is transformed to a colloidal form of palladium which becomes firmly keyed to the etched irregularities of the base.
The excess of solution is thoroughly rinsed off. There is applied to the clean wet surface a solution of a copper salt such as copper sulfate, containing sodium hydroxide and Rochelle salts and formaldehyde, forming a smooth, non-porous, highly adherent deposit.
The essence of the invention lies in the preliminary treatment of the base, which may be other resins or plastic non-conducting materials than acrylic resins. This treatment is by a substantially water-free solution of the stannous chloride in the glycols described herein. It eliminates the necessity for such pretreatments of the base as degreasing, abrading, cleaning, etc. It combines three steps of the prior art into one step and avoids the necessity of heating in the operation.
While the invention has been described by an example in which a certain proportion of the stannous chloride was used in solution in the glycol ether, such proportions may be varied within the scope of the invention. The procedure subsequent to the sensitizing may be that known in the art which includes the activation of the surface of the base with salts of palladium, gold, platinum and others. The strengths of the acid palladium solutions may vary over a considerable range, as is known. The electroless copper solutions for plating the sensitized base are also well known and have been described in the literature. The present process is useful for many purposes, as in the making of printed circuits, the coating of such non-conductive bodies as car handles, boat lighting fixtures and lamps, and many other items.
What is claimed is:
1. A method of treating a substantially non-conducting plastic base for electroless plating of a metal thereon which comprises preparing a solution consisting essentially of a reducible stannous compound in a glycol ether selected from the class consisting of the alkyl ethers of ethylene glycol, diethylene glycol, and propylene glycol wherein the alkyl radicals have from 1 to 5 carbon atoms, and contacting said base with said solution for a sufficient time to etch the surface of said base, and then washing said treated base to remove excess of said solution.
2. A method of treating in accordance with claim 1 in which said solution contains at least 0.1% of said stannous compound.
3. A method of treating in accordance with claim 1 in which said compound is stannous chloride.
4. A method of treating in accordance with claim 1 in which said solution contains at least 0.1% of said stannous compound and up to saturation.
5. A method of treating in accordance with claim 1 in which said solution contains from about 0.1% to 5.0% of said stannous compound.
6. A method of treating in accordance with claim 1 in which said contacting is conducted at approximately room temperatures.
7. A method of treating in accordance with claim 1 in which the time of contact is from about 1 to 10 minutes.
8. A method of treating in accordance with claim 1 in which the time of contact is from about 5 to 8 minutes.
9. A method of treating in accordance with claim 1 in which there is present in said solution hydrochloric acid.
10. A composition for treating a substantially nonconducting plastic base for electroless plating consisting essentially of a solution in a glycol ether selected from the class consisting of the alkyl ethers of ethylene glycol, diethylene glycol, and propylene glycol wherein the alkyl radicals have from 1 to 5 carbon atoms of about 0.1% to saturation of stannous chloride.
References Cited UNITED STATES PATENTS 2,602,757 7/1952 Kantrowitz et al. 11747 XR MAYER WEINBLATT, Primary Examiner.
U.S. Cl. X.R.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US59495266A | 1966-08-26 | 1966-08-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3425946A true US3425946A (en) | 1969-02-04 |
Family
ID=24381098
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US594952A Expired - Lifetime US3425946A (en) | 1966-08-26 | 1966-08-26 | Electroless plating composition |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3425946A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3524754A (en) * | 1967-04-28 | 1970-08-18 | Shell Oil Co | Metal plating of plastics |
| US3790400A (en) * | 1972-07-24 | 1974-02-05 | Macdermid Inc | Preparation of plastic substrates for electroless plating and solutions therefor |
| US3819526A (en) * | 1970-12-23 | 1974-06-25 | Philadelphia Quartz Co | Coated detergent compositions |
| US3898136A (en) * | 1973-03-19 | 1975-08-05 | Mitsubushi Gas Chemical Compan | Process for coating shaped resin articles |
| US4160050A (en) * | 1976-04-13 | 1979-07-03 | Kollmorgen Technologies Corporation | Catalyzation processes for electroless metal deposition |
| US4241105A (en) * | 1979-12-17 | 1980-12-23 | Western Electric Company, Inc. | Method of plating the surface of a substrate |
| EP0040090A1 (en) * | 1980-05-12 | 1981-11-18 | Macdermid, Incorporated | Process for mechanically depositing heavy metallic coatings |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2602757A (en) * | 1948-04-09 | 1952-07-08 | Morris S Kantrowitz | Method and composition for producing silver coatings |
-
1966
- 1966-08-26 US US594952A patent/US3425946A/en not_active Expired - Lifetime
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2602757A (en) * | 1948-04-09 | 1952-07-08 | Morris S Kantrowitz | Method and composition for producing silver coatings |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3524754A (en) * | 1967-04-28 | 1970-08-18 | Shell Oil Co | Metal plating of plastics |
| US3819526A (en) * | 1970-12-23 | 1974-06-25 | Philadelphia Quartz Co | Coated detergent compositions |
| US3790400A (en) * | 1972-07-24 | 1974-02-05 | Macdermid Inc | Preparation of plastic substrates for electroless plating and solutions therefor |
| US3898136A (en) * | 1973-03-19 | 1975-08-05 | Mitsubushi Gas Chemical Compan | Process for coating shaped resin articles |
| US4160050A (en) * | 1976-04-13 | 1979-07-03 | Kollmorgen Technologies Corporation | Catalyzation processes for electroless metal deposition |
| US4241105A (en) * | 1979-12-17 | 1980-12-23 | Western Electric Company, Inc. | Method of plating the surface of a substrate |
| EP0040090A1 (en) * | 1980-05-12 | 1981-11-18 | Macdermid, Incorporated | Process for mechanically depositing heavy metallic coatings |
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