US3753882A - Method for converting aluminum and aluminum base,and copper and copper base material surfaces from a hydrophobic to a hydraphilic state - Google Patents
Method for converting aluminum and aluminum base,and copper and copper base material surfaces from a hydrophobic to a hydraphilic state Download PDFInfo
- Publication number
- US3753882A US3753882A US00232608A US3753882DA US3753882A US 3753882 A US3753882 A US 3753882A US 00232608 A US00232608 A US 00232608A US 3753882D A US3753882D A US 3753882DA US 3753882 A US3753882 A US 3753882A
- Authority
- US
- United States
- Prior art keywords
- copper
- aluminum
- bath
- square foot
- base
- 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
Links
- 229910052782 aluminium Inorganic materials 0.000 title abstract description 49
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title abstract description 49
- 238000000034 method Methods 0.000 title abstract description 44
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title abstract description 42
- 239000010949 copper Substances 0.000 title abstract description 42
- 229910052802 copper Inorganic materials 0.000 title abstract description 42
- 230000002209 hydrophobic effect Effects 0.000 title abstract description 6
- 239000000463 material Substances 0.000 title description 21
- 239000002585 base Substances 0.000 title description 2
- 229910021538 borax Inorganic materials 0.000 abstract description 31
- 239000004328 sodium tetraborate Substances 0.000 abstract description 31
- 235000010339 sodium tetraborate Nutrition 0.000 abstract description 31
- 239000011248 coating agent Substances 0.000 abstract description 11
- 238000000576 coating method Methods 0.000 abstract description 11
- 239000003973 paint Substances 0.000 abstract description 10
- 239000004593 Epoxy Substances 0.000 abstract description 4
- 229920000877 Melamine resin Polymers 0.000 abstract description 4
- 238000009713 electroplating Methods 0.000 abstract description 4
- 239000004816 latex Substances 0.000 abstract description 4
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 abstract description 4
- 230000005660 hydrophilic surface Effects 0.000 abstract description 3
- 239000000080 wetting agent Substances 0.000 description 10
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 8
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 8
- 239000004141 Sodium laurylsulphate Substances 0.000 description 8
- 239000008139 complexing agent Substances 0.000 description 8
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 8
- 238000007747 plating Methods 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- 238000011282 treatment Methods 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 5
- 229910000906 Bronze Inorganic materials 0.000 description 4
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 4
- 239000010974 bronze Substances 0.000 description 4
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 4
- 229960001484 edetic acid Drugs 0.000 description 4
- 229910052759 nickel Inorganic materials 0.000 description 4
- KERTUBUCQCSNJU-UHFFFAOYSA-L nickel(2+);disulfamate Chemical compound [Ni+2].NS([O-])(=O)=O.NS([O-])(=O)=O KERTUBUCQCSNJU-UHFFFAOYSA-L 0.000 description 4
- 229910000881 Cu alloy Inorganic materials 0.000 description 3
- 230000004913 activation Effects 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 229920000126 latex Polymers 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- AEQDJSLRWYMAQI-UHFFFAOYSA-N 2,3,9,10-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline Chemical compound C1CN2CC(C(=C(OC)C=C3)OC)=C3CC2C2=C1C=C(OC)C(OC)=C2 AEQDJSLRWYMAQI-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 230000000536 complexating effect Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000002848 electrochemical method Methods 0.000 description 2
- 239000002659 electrodeposit Substances 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000009972 noncorrosive effect Effects 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- -1 polypropylene Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 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 2
- 239000001509 sodium citrate Substances 0.000 description 2
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 2
- 235000011083 sodium citrates Nutrition 0.000 description 2
- 239000000176 sodium gluconate Substances 0.000 description 2
- 229940005574 sodium gluconate Drugs 0.000 description 2
- 235000012207 sodium gluconate Nutrition 0.000 description 2
- 235000011006 sodium potassium tartrate Nutrition 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910001369 Brass Inorganic materials 0.000 description 1
- 101710184444 Complexin Proteins 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 241001275902 Parabramis pekinensis Species 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 238000007743 anodising Methods 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000011109 contamination Methods 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
- DOBRDRYODQBAMW-UHFFFAOYSA-N copper(i) cyanide Chemical compound [Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000000700 radioactive tracer Substances 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25F—PROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
- C25F1/00—Electrolytic cleaning, degreasing, pickling or descaling
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D11/00—Electrolytic coating by surface reaction, i.e. forming conversion layers
- C25D11/02—Anodisation
- C25D11/04—Anodisation of aluminium or alloys based thereon
- C25D11/06—Anodisation of aluminium or alloys based thereon characterised by the electrolytes used
- C25D11/08—Anodisation of aluminium or alloys based thereon characterised by the electrolytes used containing inorganic acids
Definitions
- a method of converting an aluminum or aluminum base article surface from a hydrophobic to a hydrophilic state comprising the steps of making the surface to be converted the anode in a bath comprising an acid-free aqueous borax solution at a temperature between 100 and 200 F., and maintaining an applied anode current at a current density not exceeding 5 amperes/ square foot for a total current application maximum of 300 coulombs/square foot.
- the hydrophilic surface produced is exceptionally amenable to subsequent coating by various paints such as epoxy base, melamine base, latex, oil base, etc.
- Copper and copper base surfaces are similarly made hydrophilic in the same bath but with the difference in that the copper surface is made the cathode, the current density is at least 1 ampere/square foot, and minimum total current application of 30 coulombs/square foot is utilized.
- the bath need not be acid-free.
- the hydrophilic surface so made is extremely amenable to subsequent electroplating, resulting in improved adhesion.
- This invention relates to electrochemical methods of preparing a surface for subsequent coating, particularly aluminum and copper surfaces, by use of a heated bath comprising an aqueous borax solution acid-free in the case of aluminum.
- Aluminum and aluminum base materials, and copper and copper base materials are two of the most widely used materials as bases for plating and painting, and for general coating applications.
- the surfaces of such materials can generally be prepared in the case of copper for subsequent plating, and in the case of aluminum for subsequent painting, by use of electrochemical methods.
- aluminum surfaces may be anodized utilizing sulphuric acid or chromic acid treatments, preparatory to subsequent coating by epoxy resin base paints, latex base paints, oil base paints, or polyurethane base paints, for example.
- copper surfaces are often prepared for subsequent coating by electroplating by use of ammonium persulfate activation, or by copper cyanide electrolytic strikes. While these are roughening treatments, the use of these is to assure good adhesion of subsequent electrodeposits such as those from a Watts nickel bath, sulfamate nickel bath, acid copper bath, etc.
- the method of this invention comprises the process of utilizing an aqueous borax solution (acid-free for aluminum) maintained at a temperature of substantially -200 F., placing two electrodes in the bath, one of which is the article surface to be converted to a hydrophilic state, and applying a current across the electrodes through the bath.
- aqueous borax solution acid-free for aluminum
- the article surfaces must be the anode, and the current density does not exceed 5 amperes/ square foot for a total current application not exceeding 300 coulombs/ square foot.
- copper is made the cathode, with a current density of at least one ampere/square foot for a minimum current application of at least 30 coulombs/square foot.
- wetting and complexing agents may also be utilized in this bath.
- a common analysis of equipment is utilizable in both cleaning methods.
- an aqueous borax solution is utilized in a tank that is non-corrosive and non-reactive with the borax solution, when the solution is heated in a temperature range of substantially 100- 200 F.
- the borax solution may vary in concentration from a quarter ounce per gallon to saturation amounts at the temperature involved.
- the solution is maintained acid-free for aluminum. Acid use does not appear to alfect the copper bath.
- both for copper and aluminum an additional electrode is necessary utilizing the borax bath as the electrolyte.
- the electrode should be non-corrosive or non-reactive with the bath at the temperature involved, and may be copper, stainless steel, lead or gold, as examples.
- both materials, the aluminum or aluminum base materials on the one hand and the copper and copper base materials on the other hand should be precleaned prior to the treatment to be described. This essentially means eliminating grease and dirt from the surfaces of the materials.
- cleaning methods are known in the art, such as vapor degreasing, acid dipping in nitric acid, inhibited alkaline cleaning, and the use in general of deoxidizers and desmutters. Where a freshly machined surface is utilized, only vapor decreasing may be necessary.
- general acid dips such as in hydrochloric acid, is sufficient.
- Other techniques for copper also well known in the art.
- a pre-cleaned aluminum surface may be placed into a heated bath comprising an acid-free aqueous borax solution, heated to a temperature of between substantially 100-200 F.
- the aluminum surface is made one of two electrodes in the bath, the other electrode being one of the common materials above.
- a current is applied across the electrodes through the bath acting as the electrolyte, with the aluminum surface being made the anode, and the current density controlled not to exceed amperes/ square foot at the article surface.
- the current is maintained for a time not exceeding a total current application of 300 coulombs/square foot.
- the current is discontinued the article removed from the bath, and rinsed by use of Water, alcohol, etc. and dried by spin drying, forced air drying, or other known methods.
- surfaces of aluminum or aluminum base materials prepared in this manner are extremely hydrophilic and have excellent adhesion properties for subsequent coating by epoxy resin base, epoxy phenolic, epoxy melamine, melamine, latex base paints, oil base paints, polyurethane base paints, and other commonly known paints.
- wetting agents and complexing agents may be added.
- Wetting agents are utilized for promoting uniformity of surface activation by the current and to act as supplementary cleaning agents in the removal of trace amounts of residual contaminations from the surface.
- the complexing agents are utilized to reduce the processing time and current requirements by their activating activity.
- this particular treatment causes no loss of surface brightness, as opposed to other anodizing treatments that tend to dull the surface.
- the preferred operating temperature range is within 140- 170 F., with a particular preferred temperature of 150 F. While one quarter ounce per gallon to saturation amount of borax at the operating temperature is utilizable, for aluminum, one quarter to ten ounces per gallon of borax is a preferred concentration range.
- a range of 3-6 ounces per gallon of borax is utilized, with a preferred range of l-3 amperes/ square foot, and still more preferably 2.5 amperes/square foot.
- the total current application should not exceed 300 coulombs/ square foot, with 40-75- coulombs/square foot preferred and 50 coulombs/square foot most preferred.
- Wetting agents may be utilized, particularly sodium lauryl sulphate, and most particularly sodium lauryl sulphate in a percentage of .l% on a weight/volume basis.
- a complexing agent may be utilized, particularly tetrasodium salt of ethylene diaminetetraacetic acid (EDTA), or sodium gluconate, Rochelle salts, sodium citrate, or other known complexing agents may be utilized.
- EDTA ethylene diaminetetraacetic acid
- sodium gluconate sodium gluconate
- Rochelle salts sodium citrate
- other known complexing agents may be utilized.
- optimum operating conditions have been found in a situation utilizing a borax concentration of 4 ounces per gallon at 2.5 amperes/square foot for 20 seconds at substantially 150 F.
- COPPER In the case of copper and copper base materials, the same bath is utilized. However, the acid-free requirement is waived. Acid use appears to have little or no effect upon the bath.
- the diiferences for copper is that the copper is made the cathode, whereas before, aluminum was the anode.
- copper is utilized as the cathode in the same bath comprising an aqueous borax solution at a temperature between substantially -200 F.
- the preferred range, as with aluminum, is -170" F., with a still more preferred temperature of operation of F.
- the bath be acid-free.
- a preferred concentration of borax is bet-ween one quarter ounce per gallon to saturation at the operating temperature, with a preferred operating range of 3-6 ounces per gallon of borax, and still more preferably 4 ounces per gallon.
- a minimum of one ampere/ square foot current density at the cathode surface is utilized, with a general range of 5-15 amperes/square foot preferred, with most preferably lO amperes/square foot utilized.
- a minimum of 30 coulombs/ square foot current application is utilized, with a preferred range being between 150-600 coulombs/ square foot, with 300 coulombs/square foot preferred.
- wetting agents as utilized in the aluminum bath, and the same complexing agents as utilized with the aluminum baths are utilized here.
- a preferred bath in general has 4 ounces per gallon borax concentration at 150 F. at 10 amperes/ square foot current density for approximately 30 seconds operating time. Upon removal from the bath, the article is rinsed with water, and immediately electroplated without intermediate drying.
- the surface is not attacked, and no measurable damage can be noted optically or with tracer (stylus type) instruments.
- the surface nonetheless is methodically activated and shows excellent adhesion for subsequent plating.
- Aluminum bronze materials comprising essentially 95% copper plus aluminum, silicon and cobalt, as well as unalloyed copper, and other copper alloys have been particularly used in conjunction with this bath. There is no detectable stock removal or detectable surface damage. Subsequent electrodeposits such as nickel have excellent adhesion. For example, using the preferred conditions above, nickel from a nickel sulfamate bath was successfully plated upon the copper prepared in the above manner.
- the nickel sulfamate bath utilized a half hour treatment of 40 amperes/square foot at 120 F., as known in the art. Also copper from copper sulfate bath, 40 amperes/square foot, 90 F., /2 hour. Plating adhesion was excellent meeting the requirements of US. Federal specifications (e.g. QQ-P-416), as a standard.
- aluminum bronze prepared by a three minute treatment in a borax solution at a 4-ounce per gallon concentration, containing .l% sodium lauryl sulphate as the wetting agent, the piece being held at 10 amperes/ square foot cathodic at a temperature of 140 F. was subsequently plated in a nickel sulfamate plating bath at 120 F., with a 20 amperes/ square foot current density for one hour, to put on one mil of nickel, as in the prior example.
- the plating adhesion again was excellent, as measured by the above Federal standard.
- plating was achieved after a borax activation at fom minutes at 100 F. at 10 amperes/square foot cathodic.
- Another example showed successful borox ac-- tivation with one minute at F. and ten amperes/ square foot cathodic.
- the test adhesion according to the above Federal specifications, was excellent. Unalloyed copper, brasses and other copper alloys are actually easier to) prepare for good adhesion than the aluminum bronze a ove.
- a method for converting the surface of an aluminum and aluminum base article from a hydrophobic to a hydrophilic base comprising the steps of:
- a method for converting the surface of a copper and copper base articles from a hydrophobic to a hydrophilic state comprising the steps of:
- the article surface being the cathode
- the curdensity being at least one ampere per square foot
Landscapes
- Chemical & Material Sciences (AREA)
- Metallurgy (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Electroplating Methods And Accessories (AREA)
- Electroplating And Plating Baths Therefor (AREA)
- Electrochemical Coating By Surface Reaction (AREA)
- Electrolytic Production Of Metals (AREA)
Abstract
A METHOD OF CONVERTING AN ALUMINUM OR ALUMINUM BASE ARTICLE SURFACE FROM A HYDROPHOBIC TO A HYDROPHILLIC STATE COMPRISING THE STEPS OF MAKING THE SURFACE TO BE CONVERTED THE ANODE IN A BATH COMPRISING AN ACID-FREE AQUEOUS BORAX SOLUTION ATT A TEMPERATURE BETWEEN 100 AND 200* F., AND MAINTAINING AN APPLIED ANODE CURRENT AT A CURRENT DENSITY NOT EXCEEDING 5 AMPERES/SQUARE FOOT FOR A TOTAL CURRENT APPLICATION MAXIMUM OF 300 COULOMBS/SQUARE FOOT. THE HYDROPHILLIC SURFACE PRODUCED IS EXCEPTIONALLY AMENABLE TO SUBSEQUENT COATING BY VARIOUS PAINTS SUCH AS EPOXY BASE, MELAMINE BASE, LATEX, OIL BASE, ETC. COPPER AND COPPER BASE SURFACES ARE SIMILARLY MADE HYDROPHILIC IN THE SAME BATH BUT WITH THE DIFFERENCE IN THAT THE COPPER SURFACE IS MADE THE CATHODE, THE CURRENT DENSITY IS AT LEAST 1 AMPERE/SQUAREE FOOT, AND MINIMUM TOTAL CURRENT APPLICATION OF 30 COULOMBS/SQUARE FOOT IS UTILIZED. THE BATH NEED NOT BE ACID-FREE. THE HYDROPHILIC SURFACE SO MADE IS EXTREMELY EMENABLE TO SUBSEQUENT ELECTROPLATING, RESULTING IN IMPROVED ADHESION.
Description
United States Patent METHOD FOR CONVERTING ALUMINUM AND ALUMINUM BASE, AND COPPER AND COPPER BASE MATERIAL SURFACES FROM A HYDRO- PHOBIC TO A HYDRAPIHLIC STATE Leo Missel, Palo Alto, Calif, assignor to International Business Machines Corporation, Armonk, N.Y. No Drawing. Filed Mar. 7, 1972, Ser. No. 232,608 Int. Cl. C231) 1/00, 5/50 US. Cl. 204-140 31 Claims ABSTRACT OF THE DISCLOSURE A method of converting an aluminum or aluminum base article surface from a hydrophobic to a hydrophilic state comprising the steps of making the surface to be converted the anode in a bath comprising an acid-free aqueous borax solution at a temperature between 100 and 200 F., and maintaining an applied anode current at a current density not exceeding 5 amperes/ square foot for a total current application maximum of 300 coulombs/square foot. The hydrophilic surface produced is exceptionally amenable to subsequent coating by various paints such as epoxy base, melamine base, latex, oil base, etc.
Copper and copper base surfaces are similarly made hydrophilic in the same bath but with the difference in that the copper surface is made the cathode, the current density is at least 1 ampere/square foot, and minimum total current application of 30 coulombs/square foot is utilized. The bath need not be acid-free. The hydrophilic surface so made is extremely amenable to subsequent electroplating, resulting in improved adhesion.
FIELD OF THE INVENTION This invention relates to electrochemical methods of preparing a surface for subsequent coating, particularly aluminum and copper surfaces, by use of a heated bath comprising an aqueous borax solution acid-free in the case of aluminum.
BACKGROUND OF THE INVENTION Aluminum and aluminum base materials, and copper and copper base materials are two of the most widely used materials as bases for plating and painting, and for general coating applications. The surfaces of such materials can generally be prepared in the case of copper for subsequent plating, and in the case of aluminum for subsequent painting, by use of electrochemical methods. In particular, aluminum surfaces may be anodized utilizing sulphuric acid or chromic acid treatments, preparatory to subsequent coating by epoxy resin base paints, latex base paints, oil base paints, or polyurethane base paints, for example. Similiarly, copper surfaces are often prepared for subsequent coating by electroplating by use of ammonium persulfate activation, or by copper cyanide electrolytic strikes. While these are roughening treatments, the use of these is to assure good adhesion of subsequent electrodeposits such as those from a Watts nickel bath, sulfamate nickel bath, acid copper bath, etc.
Common to both aluminum and copper surface preparations above, is the problem of safety due to the corrosive nature of the baths used, waste disposal problems, the ecological problems caused by use of such corrosive materials, the cost of the materials involved, the stability of the solutions and particularly the bath and shelf life stability, and most particularly the fact that these baths have a tendency to roughen and attack the surfaces which are being prepared for subsequent coating.
Prior art baths for aluminum have also utilized borax in solution with the addition of acids. These baths re- 3,753,882 Patented Aug. 21, 1973 quired high voltages and were self-limiting in that amperage dropped off to close to zero current density during operation, compared to a desired constant current operation.
Thus, it is an object of this invention to provide a method of preparing both aluminum and copper surfaces for subsequent coating that is (l) safe, (2) provides minimal Waste disposal problems, (3) minimizes ecological difficulties, (4) is non-hazardous, (5) is low in cost, (6) offers great solution stability, (7) oifers great bath and shelf life stability, (8) does not roughen the surface of the materials being prepared (9) does not attack the surfaces involved, and (10) results in excellent adhesion of the subsequent coating.
SUMMARY OF THE INVENTION These and other objects are met by the method of this invention, which comprises the process of utilizing an aqueous borax solution (acid-free for aluminum) maintained at a temperature of substantially -200 F., placing two electrodes in the bath, one of which is the article surface to be converted to a hydrophilic state, and applying a current across the electrodes through the bath. In the case of aluminum, the article surfaces must be the anode, and the current density does not exceed 5 amperes/ square foot for a total current application not exceeding 300 coulombs/ square foot. In the case of copper, copper is made the cathode, with a current density of at least one ampere/square foot for a minimum current application of at least 30 coulombs/square foot.
Wetting and complexing agents may also be utilized in this bath.
A detailed description of the process, and preferred embodiments utilized, toward a better understanding of the scope and advantages of this invention will best be understood in relation to the general description below.
GENERAL DESCRIPTION While the copper preparation and aluminum preparation techniques described below differ in certain aspects, a common analysis of equipment is utilizable in both cleaning methods. In both systems, an aqueous borax solution is utilized in a tank that is non-corrosive and non-reactive with the borax solution, when the solution is heated in a temperature range of substantially 100- 200 F. Thus, such common tanks such as stainless steel or polypropylene are quite acceptable. The borax solution may vary in concentration from a quarter ounce per gallon to saturation amounts at the temperature involved. The solution is maintained acid-free for aluminum. Acid use does not appear to alfect the copper bath.
Both for copper and aluminum, an additional electrode is necessary utilizing the borax bath as the electrolyte. Again, the electrode should be non-corrosive or non-reactive with the bath at the temperature involved, and may be copper, stainless steel, lead or gold, as examples. Similarly, is is evident that both materials, the aluminum or aluminum base materials on the one hand and the copper and copper base materials on the other hand, should be precleaned prior to the treatment to be described. This essentially means eliminating grease and dirt from the surfaces of the materials. For aluminum, cleaning methods are known in the art, such as vapor degreasing, acid dipping in nitric acid, inhibited alkaline cleaning, and the use in general of deoxidizers and desmutters. Where a freshly machined surface is utilized, only vapor decreasing may be necessary. In the case of copper and copper base materials, general acid dips such as in hydrochloric acid, is sufficient. Other techniques for copper also well known in the art.
3 ALUMINUM Thus, a pre-cleaned aluminum surface may be placed into a heated bath comprising an acid-free aqueous borax solution, heated to a temperature of between substantially 100-200 F. The aluminum surface is made one of two electrodes in the bath, the other electrode being one of the common materials above. A current is applied across the electrodes through the bath acting as the electrolyte, with the aluminum surface being made the anode, and the current density controlled not to exceed amperes/ square foot at the article surface. The current is maintained for a time not exceeding a total current application of 300 coulombs/square foot. Then, the current is discontinued the article removed from the bath, and rinsed by use of Water, alcohol, etc. and dried by spin drying, forced air drying, or other known methods.
It has been found that surfaces of aluminum or aluminum base materials prepared in this manner are extremely hydrophilic and have excellent adhesion properties for subsequent coating by epoxy resin base, epoxy phenolic, epoxy melamine, melamine, latex base paints, oil base paints, polyurethane base paints, and other commonly known paints.
To improve the bath properties, wetting agents and complexing agents may be added. Wetting agents are utilized for promoting uniformity of surface activation by the current and to act as supplementary cleaning agents in the removal of trace amounts of residual contaminations from the surface. The complexing agents are utilized to reduce the processing time and current requirements by their activating activity. In the case of aluminum, this particular treatment causes no loss of surface brightness, as opposed to other anodizing treatments that tend to dull the surface. For aluminum, the preferred operating temperature range is within 140- 170 F., with a particular preferred temperature of 150 F. While one quarter ounce per gallon to saturation amount of borax at the operating temperature is utilizable, for aluminum, one quarter to ten ounces per gallon of borax is a preferred concentration range. Still more preferred is the use of a range of 3-6 ounces per gallon of borax, and most preferably 4 ounces per gallon. A current density not exceeding 5 amperes/square foot is utilized, with a preferred range of l-3 amperes/ square foot, and still more preferably 2.5 amperes/square foot. The total current application should not exceed 300 coulombs/ square foot, with 40-75- coulombs/square foot preferred and 50 coulombs/square foot most preferred. Wetting agents may be utilized, particularly sodium lauryl sulphate, and most particularly sodium lauryl sulphate in a percentage of .l% on a weight/volume basis. Similarly, a complexing agent may be utilized, particularly tetrasodium salt of ethylene diaminetetraacetic acid (EDTA), or sodium gluconate, Rochelle salts, sodium citrate, or other known complexing agents may be utilized. In particular, optimum operating conditions have been found in a situation utilizing a borax concentration of 4 ounces per gallon at 2.5 amperes/square foot for 20 seconds at substantially 150 F.
It is evident that depending upon the shape of the aluminum or aluminum base article, areas can be masked to expose limited areas of the entire article, or the entire article may be placed in the bath if it is desired to subsequently coat the entire surface. The amount of area exposed is a matter of choice, but is the effective area that must be utilized in calculating the amperage per square foot and total current applied.
COPPER In the case of copper and copper base materials, the same bath is utilized. However, the acid-free requirement is waived. Acid use appears to have little or no effect upon the bath. The diiferences for copper is that the copper is made the cathode, whereas before, aluminum was the anode. Thus, copper is utilized as the cathode in the same bath comprising an aqueous borax solution at a temperature between substantially -200 F. The preferred range, as with aluminum, is -170" F., with a still more preferred temperature of operation of F.
It is preferred that the bath be acid-free. A preferred concentration of borax is bet-ween one quarter ounce per gallon to saturation at the operating temperature, with a preferred operating range of 3-6 ounces per gallon of borax, and still more preferably 4 ounces per gallon. A minimum of one ampere/ square foot current density at the cathode surface is utilized, with a general range of 5-15 amperes/square foot preferred, with most preferably lO amperes/square foot utilized. A minimum of 30 coulombs/ square foot current application is utilized, with a preferred range being between 150-600 coulombs/ square foot, with 300 coulombs/square foot preferred. The same wetting agents as utilized in the aluminum bath, and the same complexing agents as utilized with the aluminum baths are utilized here. Thus, optionally one may add sodium lauryl sulphate preferably in an amount of .l% on a weight/volume basis, and a complexing salt, preferably a tetrasodium salt such as EDTA, or the more common sodium gluconate, Rochelle salt, sodium citrate, etc. A preferred bath in general has 4 ounces per gallon borax concentration at 150 F. at 10 amperes/ square foot current density for approximately 30 seconds operating time. Upon removal from the bath, the article is rinsed with water, and immediately electroplated without intermediate drying.
As in the case of aluminum, the surface is not attacked, and no measurable damage can be noted optically or with tracer (stylus type) instruments. The surface nonetheless is methodically activated and shows excellent adhesion for subsequent plating. Aluminum bronze materials, comprising essentially 95% copper plus aluminum, silicon and cobalt, as well as unalloyed copper, and other copper alloys have been particularly used in conjunction with this bath. There is no detectable stock removal or detectable surface damage. Subsequent electrodeposits such as nickel have excellent adhesion. For example, using the preferred conditions above, nickel from a nickel sulfamate bath was successfully plated upon the copper prepared in the above manner. The nickel sulfamate bath utilized a half hour treatment of 40 amperes/square foot at 120 F., as known in the art. Also copper from copper sulfate bath, 40 amperes/square foot, 90 F., /2 hour. Plating adhesion was excellent meeting the requirements of US. Federal specifications (e.g. QQ-P-416), as a standard.
Similarly, aluminum bronze prepared by a three minute treatment in a borax solution at a 4-ounce per gallon concentration, containing .l% sodium lauryl sulphate as the wetting agent, the piece being held at 10 amperes/ square foot cathodic at a temperature of 140 F. was subsequently plated in a nickel sulfamate plating bath at 120 F., with a 20 amperes/ square foot current density for one hour, to put on one mil of nickel, as in the prior example. The plating adhesion again was excellent, as measured by the above Federal standard.
Similarly, plating was achieved after a borax activation at fom minutes at 100 F. at 10 amperes/square foot cathodic. Another example showed successful borox ac-- tivation with one minute at F. and ten amperes/ square foot cathodic. The test adhesion, according to the above Federal specifications, was excellent. Unalloyed copper, brasses and other copper alloys are actually easier to) prepare for good adhesion than the aluminum bronze a ove.
Thus, aluminum materials have been made extremely hydrophilic, for subsequent excellent adhesions of various commonly known coating materials, by the use of the borax bath under the conditions described above. Similarly, copper has been activated, including copper alloys, aluminum bronze, brass, and other copper materials, ae-
cording to use of the bath above. Subsequently electroplating adhesions are excellent.
What is claimed is: 1. A method for converting the surface of an aluminum and aluminum base article from a hydrophobic to a hydrophilic base comprising the steps of:
heating a bath comprising an acid-free aqueous borax solution to a temperature between substantially 100- 200 F.;
placing two electrodes in the bath, one of which is the article surface to be converted to a hydrophilic state; applying a current across the electrode through the bath, the article surface being made the anode, the current density not exceeding amperes per square foot at the article surface;
maintaining the applied current for a time not exceeding a total current application of 300 coulombs per square foot, and removing the article from the bath.
2. The method of claim 1 wherein the bath is heated to a temperature range of 140170 F.
3. The method of claim 1 wherein the bath is heated to a temperature of substantially 150 F.
4. The method of claim 1 wherein the bath contains a borax concentration of between one quarter to ten ounces per gallon.
5. The method of claim 1 wherein the borax concentration in the bath is between 3-6 ounces per gallon.
6. The method of claim 1 wherein the borax concentration is 4 ounces per gallon.
7. The method of claim 1 wherein the current density is between one to three amperes per square foot at the article surface.
8. The method of claim 1 wherein the current density is 2.5 amperes per square foot at the article surface.
9. The method of claim 1 wherein the applied current is maintained for a total time application of between 40-75 coulombs per square foot.
10. The method of claim 1 wherein the applied current is maintained for a time of a total current application of 50 coulombs per square foot.
11. The method of claim 1 wherein the bath includes a wetting agent.
12. The method of claim 11 wherein the wetting agent is sodium lauryl sulphate.
13. The method of claim 12 wherein the sodium lauryl sulphate is present in .1% on a weight/volume basis.
14. The method of claim 1 wherein the bath includes a complexin g agent.
15. The method of claim 14 wherein the complexing agent is tetrasodium salt of ethylenediaminetetraacetic acid.
16. A method for converting the surface of a copper and copper base articles from a hydrophobic to a hydrophilic state comprising the steps of:
heating a bath comprising an aqueous borax solution to a temperature between substantially 10020( F.,
placing two electrodes in the bath, one of which is the article surface to be converted to a hydrophilic state;
applying a current across the electrodes through the bath, the article surface being the cathode, the curdensity being at least one ampere per square foot,
maintaining the applied current for a time at least exceeding a total current application of 30 coulombs per square foot, and
removing the article from the bath.
17. The method of claim 16 wherein the bath is heated to temperature range of -170" F.
18. The method of claim 16 wherein the bath is heated to a temperature of substantially F.
19. The method of claim 16 wherein the bath contains a borax concentration of between one quarter ounce per gallon to saturation.
20. The method of claim 16 wherein the borax concentration in the bath is between 3-6 ounces per gallon.
21. The method of claim 16 wherein the borax concentration is 4 ounces per gallon.
22. The method of claim 16 wherein the current density is between 5 to 15 amperes per square foot at the article surface.
23. The method of claim 16 wherein the current density is 10 amperes per square foot at the article surface.
24. The method of claim 16 wherein the applied current is maintained for a total time application of between 150-600 coulombs per square foot.
25. The method of claim 16 wherein the applied current is maintained for a time of a total current application of 300 coulombs ped square foot.
26 The method of claim 16 wherein the bath includes a wetting agent.
27. The method of claim 26 wherein the wetting agent is sodium lauryl sulphate.
28. The method of claim 27 wherein the sodium lauryl sulphate is present in .1% on a weight to volume basis.
29. The method of claim 16 wherein the bath includes a complexing agent.
30. The method of claim 29 wherein the complexing ageit is tetrasodium salt of ethylenediaminettetraacetic ac1 31. The method of claim 16 wherein the aqueous borax solution is an acid-free aqueous borax solution.
References Cited UNITED STATES PATENTS 1,314,839 9/1919 Weeks 204-12975 2,958,610 11/1960 Ramierz 204-33 FOREIGN PATENTS 518,73 3 3/ 1940 Great Britain 20433 THOMAS TUFARIELLO, Primary Examiner US. Cl. X.R. Z0433 129,75
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US23260872A | 1972-03-07 | 1972-03-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3753882A true US3753882A (en) | 1973-08-21 |
Family
ID=22873819
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US00232608A Expired - Lifetime US3753882A (en) | 1972-03-07 | 1972-03-07 | Method for converting aluminum and aluminum base,and copper and copper base material surfaces from a hydrophobic to a hydraphilic state |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3753882A (en) |
| JP (1) | JPS5438587B2 (en) |
| DE (1) | DE2310638C2 (en) |
| FR (1) | FR2174846B1 (en) |
| GB (2) | GB1404068A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4225397A (en) * | 1978-11-06 | 1980-09-30 | Ford Motor Company | New and unique aluminum plating method |
| US4428987A (en) | 1982-04-28 | 1984-01-31 | Shell Oil Company | Process for improving copper-epoxy adhesion |
| CN102825260A (en) * | 2012-06-28 | 2012-12-19 | 北京工业大学 | Method for preparing super-hydrophilic infiltrating surface on aluminum surface |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4006363C1 (en) * | 1990-03-01 | 1991-01-17 | Heidelberger Druckmaschinen Ag, 6900 Heidelberg, De | |
| JP6081690B2 (en) * | 2009-12-22 | 2017-02-15 | 花王株式会社 | Liquid cooling method |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1532057A (en) * | 1966-07-21 | 1968-07-05 | Cooperatieve Verkopp En Produc | Process improvements for the deoxidation of copper and copper alloys |
| GB1243741A (en) * | 1969-01-31 | 1971-08-25 | Peter Neufeld | Anodising of aluminium in alkaline borate solutions |
-
1972
- 1972-03-07 US US00232608A patent/US3753882A/en not_active Expired - Lifetime
-
1973
- 1973-01-18 GB GB233675A patent/GB1404068A/en not_active Expired
- 1973-01-18 GB GB255573A patent/GB1404067A/en not_active Expired
- 1973-02-06 FR FR7305434A patent/FR2174846B1/fr not_active Expired
- 1973-02-12 JP JP1668773A patent/JPS5438587B2/ja not_active Expired
- 1973-03-02 DE DE2310638A patent/DE2310638C2/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4225397A (en) * | 1978-11-06 | 1980-09-30 | Ford Motor Company | New and unique aluminum plating method |
| US4428987A (en) | 1982-04-28 | 1984-01-31 | Shell Oil Company | Process for improving copper-epoxy adhesion |
| CN102825260A (en) * | 2012-06-28 | 2012-12-19 | 北京工业大学 | Method for preparing super-hydrophilic infiltrating surface on aluminum surface |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS49126A (en) | 1974-01-05 |
| FR2174846B1 (en) | 1976-04-09 |
| DE2310638C2 (en) | 1982-09-09 |
| JPS5438587B2 (en) | 1979-11-21 |
| FR2174846A1 (en) | 1973-10-19 |
| GB1404067A (en) | 1975-08-28 |
| DE2310638A1 (en) | 1973-09-20 |
| GB1404068A (en) | 1975-08-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4374709A (en) | Process for plating polymeric substrates | |
| US3915811A (en) | Method and composition for electroplating aluminum alloys | |
| US4601957A (en) | Method for producing a thin tin and nickel plated steel sheet for welded can material | |
| US2391289A (en) | Bright copper plating | |
| US1971761A (en) | Protection of metals | |
| US3454376A (en) | Metal composite and method of making same | |
| US2541083A (en) | Electroplating on aluminum | |
| US3753882A (en) | Method for converting aluminum and aluminum base,and copper and copper base material surfaces from a hydrophobic to a hydraphilic state | |
| US3518168A (en) | Electrolytic process of preparing a copper foil for a plastic coat | |
| US2473163A (en) | Plating nickel on aluminum | |
| US2457061A (en) | Method for bonding a nickel electrodeposit to a nickel surface | |
| US3207679A (en) | Method for electroplating on titanium | |
| US3390061A (en) | Protective localized area resin coatings for electroplating | |
| US3531379A (en) | Process of coating aluminum with other metals | |
| US2511952A (en) | Process of plating zinc on aluminum | |
| US3515650A (en) | Method of electroplating nickel on an aluminum article | |
| US2714089A (en) | Electrodepositing iron | |
| US4212907A (en) | Pre-treatment for molybdenum or molybdenum-rich alloy articles to be plated | |
| US2796361A (en) | Method of making corrosion protected articles | |
| US2557823A (en) | Method of forming a composite article comprising steel and silver | |
| US2729601A (en) | Electroplating on beryllium | |
| US2092130A (en) | Anodic cleaning process | |
| US2127640A (en) | Method of chromium plating | |
| US2118956A (en) | Method of chromium plating | |
| US1727331A (en) | Process of coating aluminum electrolytically |