AU580433B2 - Process for conditioning the surface of plastic substrates prior to metal plating - Google Patents
Process for conditioning the surface of plastic substrates prior to metal platingInfo
- Publication number
- AU580433B2 AU580433B2 AU59914/86A AU5991486A AU580433B2 AU 580433 B2 AU580433 B2 AU 580433B2 AU 59914/86 A AU59914/86 A AU 59914/86A AU 5991486 A AU5991486 A AU 5991486A AU 580433 B2 AU580433 B2 AU 580433B2
- Authority
- AU
- Australia
- Prior art keywords
- resin
- plastic
- metal
- polar material
- organic solvent
- 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.)
- Ceased
Links
- 229920003023 plastic Polymers 0.000 title claims description 33
- 239000004033 plastic Substances 0.000 title claims description 33
- 229910052751 metal Inorganic materials 0.000 title claims description 32
- 239000002184 metal Substances 0.000 title claims description 32
- 238000000034 method Methods 0.000 title claims description 32
- 238000007747 plating Methods 0.000 title claims description 25
- 230000008569 process Effects 0.000 title claims description 15
- 239000000758 substrate Substances 0.000 title claims description 10
- 230000003750 conditioning effect Effects 0.000 title claims description 8
- 229920005989 resin Polymers 0.000 claims description 36
- 239000011347 resin Substances 0.000 claims description 36
- 239000000203 mixture Substances 0.000 claims description 35
- 239000000463 material Substances 0.000 claims description 26
- 238000005530 etching Methods 0.000 claims description 15
- 239000003960 organic solvent Substances 0.000 claims description 13
- 239000004697 Polyetherimide Substances 0.000 claims description 12
- 229920001601 polyetherimide Polymers 0.000 claims description 12
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 9
- 238000000576 coating method Methods 0.000 claims description 8
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 7
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000011248 coating agent Substances 0.000 claims description 6
- 230000001143 conditioned effect Effects 0.000 claims description 5
- 150000002500 ions Chemical class 0.000 claims description 5
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical group COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 claims description 4
- 230000001070 adhesive effect Effects 0.000 claims description 4
- 239000011521 glass Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 230000003213 activating effect Effects 0.000 claims description 3
- 229910001430 chromium ion Inorganic materials 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 238000009713 electroplating Methods 0.000 claims description 3
- 230000001235 sensitizing effect Effects 0.000 claims description 2
- 229960001760 dimethyl sulfoxide Drugs 0.000 claims 2
- 239000000243 solution Substances 0.000 description 19
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 14
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 11
- 239000010949 copper Substances 0.000 description 11
- 229910052802 copper Inorganic materials 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical group [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- -1 ethylene glycol Chemical class 0.000 description 5
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 4
- 239000012190 activator Substances 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 239000003638 chemical reducing agent Substances 0.000 description 4
- 150000002170 ethers Chemical class 0.000 description 4
- 229910052763 palladium Inorganic materials 0.000 description 4
- 229940032330 sulfuric acid Drugs 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- 230000000630 rising effect Effects 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- HUHGPYXAVBJSJV-UHFFFAOYSA-N 2-[3,5-bis(2-hydroxyethyl)-1,3,5-triazinan-1-yl]ethanol Chemical compound OCCN1CN(CCO)CN(CCO)C1 HUHGPYXAVBJSJV-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 229920004738 ULTEM® Polymers 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 238000007772 electroless plating Methods 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 230000001976 improved effect Effects 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000003313 weakening effect Effects 0.000 description 2
- AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- MIMUSZHMZBJBPO-UHFFFAOYSA-N 6-methoxy-8-nitroquinoline Chemical compound N1=CC=CC2=CC(OC)=CC([N+]([O-])=O)=C21 MIMUSZHMZBJBPO-UHFFFAOYSA-N 0.000 description 1
- 241000272470 Circus Species 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 229940113088 dimethylacetamide Drugs 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- ROZPNEGZBIUWBX-UHFFFAOYSA-N n-[bis(diethylamino)phosphoryl]-n-ethylethanamine Chemical compound CCN(CC)P(=O)(N(CC)CC)N(CC)CC ROZPNEGZBIUWBX-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- RAOIDOHSFRTOEL-UHFFFAOYSA-N tetrahydrothiophene Chemical group C1CCSC1 RAOIDOHSFRTOEL-UHFFFAOYSA-N 0.000 description 1
- 229910001432 tin ion Inorganic materials 0.000 description 1
- IUTCEZPPWBHGIX-UHFFFAOYSA-N tin(2+) Chemical compound [Sn+2] IUTCEZPPWBHGIX-UHFFFAOYSA-N 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K3/00—Apparatus or processes for manufacturing printed circuits
- H05K3/38—Improvement of the adhesion between the insulating substrate and the metal
-
- 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
- C23C18/24—Roughening, e.g. by etching using acid aqueous solutions
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K3/00—Apparatus or processes for manufacturing printed circuits
- H05K3/38—Improvement of the adhesion between the insulating substrate and the metal
- H05K3/381—Improvement of the adhesion between the insulating substrate and the metal by special treatment of the substrate
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/03—Use of materials for the substrate
- H05K1/0313—Organic insulating material
- H05K1/032—Organic insulating material consisting of one material
- H05K1/0346—Organic insulating material consisting of one material containing N
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K2203/00—Indexing scheme relating to apparatus or processes for manufacturing printed circuits covered by H05K3/00
- H05K2203/07—Treatments involving liquids, e.g. plating, rinsing
- H05K2203/0779—Treatments involving liquids, e.g. plating, rinsing characterised by the specific liquids involved
- H05K2203/0783—Using solvent, e.g. for cleaning; Regulating solvent content of pastes or coatings for adjusting the viscosity
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K3/00—Apparatus or processes for manufacturing printed circuits
- H05K3/10—Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern
- H05K3/18—Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern using precipitation techniques to apply the conductive material
- H05K3/181—Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern using precipitation techniques to apply the conductive material by electroless plating
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Manufacturing & Machinery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemically Coating (AREA)
- Manufacturing Of Printed Wiring (AREA)
- Electroplating Methods And Accessories (AREA)
Description
Description
PROC ESS FOR CONDITIONING TH E SURFAC E OF PLASTIC SUBSTRATES P RIOR TO M ETAL PLATING
Technical Field
This inv ention relates to the metal plating of plastics and, in particular, to enhancing the adhesion of metal plating to polyetherimide plastics, such as, the plastic sub st rate of elect ronic circu it boards, by conditioning the board p rior to metal plating of the board.
Backg round Art
The metal plating of plastic parts is well-known to be of considerable commercial importance because the desirable characteristics of both the plastic and the metal are combined to offer the technical and aesthetic advantag es of each. Thus, a part plated with a b right, metallic finish tak es advantag e of the economies in cost and weight afforded by substituting mold ed plastic parts for metal and, additionally, the plated finishes are not as susceptible to pitting and corrosion because there is no galvanic reaction between a plastic substrate and a plated metal. Such metal plating of plastics is used for a wide range of applications f rom decorative plating to radio f requency shielding.
An important process is the preparation of electronic circuit boards which requires the electroless plating of a conductive metal layer, usually copper, onto the plastic substrate of the board. At present, boards are predominately made of epoxy resins but there is a constant search for different materials which will offer improved economies and other benefits. One such material is a olyetherimide resin which has a higher temperature stability than epoxy and which can be injection molded with through-holes, thus eliminating the costly drilling step now required when preparing epoxy boards. Resins of this type are made by General Electric Company under the trademark ULTEM. For convenience the following description will relate specifically to the process for conditioning polyetherimi e resins although it will be understood that the process may be suitably employed for other resin materials.
These boards vary in design and may have a copper layer on each surface face of the polyetherimide resin (two-sided boards) or they can be multi-layer boards which have a plurality of inter-leaved parallel planar copper and resin layers. In both type boards through-holes in the boards are metal ' plated to facilitate connection between the circuits on the copper layers. The problems in plating either the through-holes or other plastic parts of the board are well-known in the art and a number of methods have been developed to improve the adhesion of the metal plating to the plastic substrate.
While different uses require different adhesive strengths, in general, it has been established that a minimum peel strength of about 8 lbs. per linear inch (approximately 1.4 kilograms per centimeter) as measured by the Jacquet Peel Test is required to prevent a metal coating from blistering or peeling from a plastic surface during manufacture and use. According to ASEP
Guidelines, the test measures the force needed to peel a one-inch (2.5 centimeters) wide plate strip 37.5 micrometers ± 0.51 thick acting at 90° ± 5° to the substrate surface. The measurement is done with an Instron Tensometer programmed to peel the plate strip from the substrate. at the rate of 1.0 + 0.1 inch (2.5 + 0.2 centimeters) per minute.
The present invention treats the plastic surface before plating to enhance the adhesiveness of the metal plating using a procedure generally known as a swell and etch technique and employs solvents which condition or swell the plastic and oxidants to etch the plastic. U.S. Patent No. 3,758,332 discloses the use of chemicals such as methyl ethyl ketone, tetrahydrofuran, dioxane, pyridine, dimethylf orma ide, and an alcohol mixture comprising methyl ethyl ketone, ethanol and methanol as SWellants for epoxy resin. The swelled plastic is then exposed to an etchant for a sufficient period of time to etch the swelled surface without unduly weakening or otherwise adversely affecting the physical characteristics of the plastic. Etchants are oxidizing materials and are generally aqueous solutions containing materials such as sulfuric acid, phosphoric acid, permanganate ions, Cr+6 ions and the like. U.S. Patent No. 4,086,128 shows pretreatment of an epoxy resin with an organic solvent comprising alcohols, acids, esters, ketone, nitriles, nitro compounds, and polyhydric
compounds such as ethylene glycol, gylcerine and 1, 2-p ropylene gylcol p rior to etching with hydrogen peroxide and sulfu ric acid. U.S. Patent No. 3,865,623 shows immersion of expoxy resin in an organic solvent 5 such as dimethylformamide to render the epoxy receptive to an acid etch. The disclosu res of the above publications are hereby incorporated by reference.
To be commercially useful, however, it is important 10 that the swell and etch process provide a consistent and reproducible resin conditioning effect which results in the minimum peel strength being achieved practically for g reater than 99% of the parts being conditioned and plated. Without this reproducibility the costs to the ---5 printed circuit board industry would be staggering and result in highly increased manufactu ring expenses.
Disclosu re of Invention 20
It has now been discovered that the adhesiveness of metal plating and, in particular, electroless metal plating, to plastics such as polyetherimide can be enhanced by a swell and etch process using specially
25 formulated compositions und er controlled op erating conditions. The method includes first exposing the plastic for a suitable time to a swellant composition comprising a solution of a polar material, preferably having a dielectric constant g reater than about 15 and a
30 dipole moment g reater than about 3 Debye Units (D) and an org anic solvent such as a carboxylic acid, ketone, hyd rocarbon, ether, ester, alcohol, p olyhyd ric, e.g., glycol and gylcol ethers and esters. The swelled plastic is then exposed to an etchant comprising C r+6 ions,
35 an d , p r ef erably, also including an acid such as
H2S04 , at an elevated temperatu re, e.g., above about 160°F., for a sufficient period to etch the swelled su rface without unduly weakening or otherwise adversely affecting the physical characteristics of the plastic.
The resultant etched su rface is now in a condition of improved adhesion for any species such as p rinting inks, paints, coatings, and, in particular, for metal coatings, which may be deposited thereon. As will be app reciated by those skilled in the art, rinsing of the plastic may be performed at any stage of the process and removal of residual etchant or etchant-plastic material may require fu rther treatment if desired.
In general, the process of using the compositions of the invention in manufactu ring printed circuit boards and,- in particular, boards containing through-holes, is a sequ ence of steps comm encing with a laminate or multi-lamin ate m ade f rom, e.g., filled polyetherimide material. A predesigned series of through-holes may be formed in the board by injection molding or d rilling. The board is then contacted with the swellant composition of the invention and, after water rinsing, the board is etched at an elevated temperatu re with an oxidant such as a solution of H2 S04 and C r03 and w ater rin sed. Treatment with a reductant to lower the oxidation state of the chrome residues is then typically performed and the board rinsed providing a board ready for electroless metal plating using conventional p rocedu res. A p referred step is to pretreat the board with a composition such as ENPLATE PC-4459 sold by Enthone, Incorporated to remove hyd rocarbon soils and promote the catalyst and then to contact the board with a composition such as ENPLATE PC-236 to eliminate d rag-in. The board is now immersed in a catalyst, such as a tin-palladium solution, which
conditions the surface of the resin for electroless copper plating. ENPLATE Activator 444 is exemplary of this type of catalyst. The board is then immersed in a post activator such as ENPLATE PA-493 to activate the Scatalyst by removing the excess tin and freeing the metal palladium ions on the board, rinsed and immersed in an electroless copper plating solution for a period of time sufficient to plate copper to the desired thickness on the surfaces and to plate the surfaces of the holes to lOform through-hole connections between the laminate surfaces. ENPLATE CU-700 and other similar plating compositions may be employed. The boards may then be immersed in dilute sulfuric acid followed by electroplating using conventional techniques if a thicker
15coating is desired. Rinsing of the board between steps may be conventionally employed as is well-known in the art.
20Modes for Carrying Out The Invention
It is preferred that the polyetherimide resin contain other materials, preferably a filler or reinforcing material, e.g., glass fibers. Other fillers include
2 >aper, synthetic fibers, carbon black, alumina powders, silica powders, wax, etc. Pigments, mold release agents, and other conventional additives may also be employed in the resin for specific purposes.
30 It has been found that a swellant pretreat ent is necessary to enable the etching process to roughen, or to otherwise condition, the surface and to provide the enhanced adhesion of the invention. The swellant composition comprises a solution of a polar material and
35an organic solvent, which composition is essential to
provide a swelled plastic capable of being etched and plated with the desired adhesiveness at a high degree of reproducability as will be demonstrated in the examples.
The polar materials useful herein are those materials having dielectric constants greater than about 15, preferably greater than about 20, most preferably greater than about 30 and dipole moments greater than about 3 D and preferably greater than about 3.5 D. Exemplary of these materials are dimethylformamide, dimethylacet amide, dimethyl sulfoxide, tetrahydrothiophene dioxide, N-methylpyrrolidone, hexa ethylphosphoric triamide, tetramethylurea, and acetonitrile. Other materials of similar structures may also be utilized as the polar materials hereof. Thus, other sulfoxides which are liquid at or near room temperature may be so employed, e.g., those having the formula
"
R-S-Rl
wherein R and Rl may each comprise alkyl groups of from 1 to 4 carbon atoms. Similarly, other sulfones may be so used, e.g., those of the formula
R2-S02-R3
wherein R2 and R3 may be lower alkyl (1 to 4 carbon atoms) or may be linked to form a tetrahydrothiophene ring.
The second component of the swellant composition may be any suitable organic solvent selected from the carboxylic acids, ketones, hydrocarbons, ethers, esters.
alcohols, polyhydrics, e.g., glycols and polyglycols, including ethers and esters thereof. In general, the organic solvent will typically contain less than about 10 carbon atoms, with the proviso that the polar material be soluble in the organic solvent to produce the desired composition. Exemplary solvents include acetic acid, n-pentane, ethyl acetate, ethanol, methoanol, and the like.
The preferred organic solvents because of their demonstrated effectiveness are the polyhydrics such as the glycols, and the ethers and esters thereof. These solvents may be represented by the formula
RlO(AO)nR2 wherein Rl and R2 are independently selected from the group consisting of hydrogen atoms, aryl groups and alkyl and acyl groups of 1-4 carbon atoms, A is a straight or branched chain C2 to C4 alkylene group, and n is an integer of 1 to 4. Examples of these solvents include ethylene glycol, ethylene glycol m on om ethyl ether, propylene glycol, propylene glycol monomethyl ether, ethylene glycol acetyl ester, etc.
It will be appreciated by those skilled in the art that the polar material and organic solvent swellant mixture may comprise one or more compounds of each ingredient. The swellant composition may also be used in the form of an aqueous solution although it has been found that the water is desirably limited, in weight percent, to less than about 20%, and preferably less than 10% and more preferably less than 5% and even 1%. In general, water decreases the swellant effect of the composition and the adhesiveness of the subsequent metal plating.
Two particularly preferred polar materials are dim ethylsu If o ide (DMSO) and N-methylpyrr olid one and the preferred solvents are the polyhydrics represented by the formula RlO(AO)nR2. In general, compositions of the two components contain, by volume, about 25% to 90% DMSO, preferably 50% to 85% and most preferably 70% to 80%, with the balance being the polyhydric component. For compositions containing N-methylpyrrolidone a range of 15% to 70%, preferably 20% to 50% and most preferably 20% to 30% may be employed. A preferred solvent because of its demonstrated effectiveness is propylene glycol onomethyl ether wherein Rl is H, A is C3, n is 1 and R2 is methyl.
Suitable additives can be employed in the swellant composition for specific purposes such as wetting agents to enhance the capability of spreading the composition on the resin surface.
To practice the method of the invention the plastic substrate is contacted with the swellant composition at an elevated temperature for a sufficient time to render the surface receptive to the etching process. Contacting procedures may vary widely, e.g., 1 to 60 minutes at temperatures up to about 180°F. (82°C), and preferably 2 to 20 minutes at 140° to 160°F. (60° to 71°C). Satisfactory results for glass-filled polyetherimide resin are provided by immersing the part in the composition for about 5 minutes at 150°F. (65°C). The time and temperature will, in general, vary inversely as will be appreciated by those skilled in the art. Other means such as spraying, may be used for treating the plastic part.
The treated plastic part is then ready for oxidative
etching using a chrome containing solution and basically comprises contacting the treated plastic part with the etchant at an elevated temperature for a sufficient time to promote adhesion to the surface. It is preferred to then rinse the etched plastic part to remove excess solution and to remove any chrome residues by neutralization with a material such as sodium bisulfite or chemical reduction using reductants such as hydrazine and oxalic acid.
The aqueous chrome containing etchant solutions are well-known in the art and preferably comprise Cr+6 ions, e.g., Cr207= and Crθ3. An acid such as
H2S04 is preferably included in the etchant solution and other acids like H3P04 may also be employed. A preferred etchant composition is an aqueous solution of H2S04 and Cr03. Suitable additives may also be used such as surfactants, e.g., perf luorinated sulfonates, to insure uniform etching of the conditioned resin surface. The concentration of the etchant solution may vary widely with the chromium component added as Cr03 being, by weight, about 100 grams/liter (g/1) to saturation, preferably about 200 to 600 g/1, and most preferably about 300 to 500 g/1. The acid component is about 100 to 500 g/1, and more preferably about 200 to 400 g/1. A preferred composition contains about 400-450 g/1 Cr03, e.g., 420 g/1, and 250-350 g/1 H2S04, e.g., 300 g/1.
An important feature of the invention is the temperature of the etching process. Conventional etching procedures utilize a temperature which may vary over a broad spectrum from as low as room temperature to the boiling point of the etching solution. It has been found for the conditioned polyetherimide resins however, that
temperatu res above about 160°F. (71°C) and p referably above about 170°F. (77°C) are n ecessary and that unexpected adhesive p roperties to the metal coating are p rovided. While the etching time will vary depending on the concentration of the etching solution and temperatu re of the etching p rocess as will be app reciated by those skilled in the art, for the p referred composition of 420 g/1 C r03 and 300 g/1 H2 S04 , an etching time of about 5-15 minutes at 170°F. (77°C) p rovides excellent results. In general, the etching time may be up to about 60 minutes but is typically less than 30 minutes.
It is to be understood and stressed for both the s w ellant and etchant p rocedu res, that the above concentrations, temperatu res and time parameters are all interdependent and that variations in temperatu re will p roduce variations in the other parameters whereby optimum results will be attained. In this regard, the variou s parameters and their interdepend ency are well known in the art and their interaction between one another is also well known or can be easily ascertained experimentally by one skilled in the art.
An optional step of removing traces of deposits on the etched resin may now be performed. Rinsing will remove deposits but a p referred p rocedu re is to contact the resin with a suitable reducing ag ent for chromium ions such as NaHS03 , NaOH, and the lik e. Immersion of the etched resin in a solution of 150 g/1 NaHS03 for 5 minutes has p roduced satisfactory results. Typically, exposu re to the reducing agent rang es f rom 30 seconds to 10 minutes at a temperatu re ranging f rom room temperatu re to 160°F. (71°C).
If a smoother metal plated su rface is desired, another
optional step is to treat the etched resin to dissolve part of the filler material. Materials such as hydrogen fluoride and ammonium bifluoride may be suitably employed. ACTANE 70 sold by Enthone, Incorporated has proven very satisfactory for this purpose.
The etched resin is now prepared for metal plating by known means to render the surface catalytic. Among them are cleaning, applying catalyst promoters, sensitizing using an aqueous tin chloride solution and then activating by means of palladium chloride. On the other hand, unitary baths may be employed for such purposes, such as the dispersions of colloidal palladium and tin ions described in Shipley, U.S. Patent No. 3,011,920 or the soluble complexes of noble metals, stannous ion and anions as described in Zeblisky, U.S. Patent No. 3,672,938. The surface may now be plated, with a film of metal by 'electroless' plating. Activating and plating compositions and methods for copper metal electroless deposition are described in U.S. Patent Nos. 2,874,072; 3,011,920; 3,075,855; 3,095,309; 3,672,938; and 3,736,156; the disclosures of said patents being hereby incorporated reference. Other methods of deposition may also be used such as vacuum vapor deposition, electrolytic plating or a combination of electroless plating and electorlytic plating.
The present invention will now be described in detail by reference to the following examples.
EXAMPLE I
The following example illustrates the process of using the swellant and etchant compositions to enhance the adhesiveness of electroless plated copper to glass-filled polyetherimide resin.
An injection molded plaqu e of ULTEM glass-filled polyetherimide resin was metallized using the following p rocedu re:
(a) immerse the plaqu e for 5 minutes at 150°F. (65°C) with mild agitation in a solution comp rising, by volume, 75 % DMSO and 25 % propylene glycol monomethyl ether (PGMM E);
(b) rinse for 5 minutes in running water;
(c) etch for 10 minutes at 170°F. (77°C) with mild agitation in a solution comp rising 420 g/1 C r03 and 3 00 g/1 H2S04 ;
(d) rinse for 5 minutes in running water;
(e) neutralize for 5 minutes at room temperatu re in a solution comp rising 150 g/1 NaHS03 ; (f) rinse in running water for 5 minutes;
(g) immerse in conditioning cleaner ENPLATE PC-4459 for 5 minutes at 150°F. (65°C);
(h) rinse in running water for 5 minutes: (i) immerse in ENPLATE PC-236 for 2 minutes at room temperatu re;
(j) immerse in one-step palladium catalyst ENPLATE Activator 44 for 5 minutes at 75°F. (24°C); (k) rinse with running water;
(1) immerse in post activator solution ENPLAT E PA-493 for 5 minutes at room temperatu re;
(m) rinse in running water for 5 minutes; (n) plate in an electroless copper solution ENPLATE CU-700 for 30 minutes at 118°F. (48°C); (o) rinse with running water; (p) immerse in 3 % sulfu ric acid for 1 minute;
(q) electroplate in an acid copper electrolyte to about 0.001 inch (25 microns);
(r) rinse with running water for 2 minutes; and (s) air dry.
The metal layer was tested for adhesion using the Jacquet Peel Test and an ultimate peel strength of greater than 11 lbs/in (2 kilograms/cm) was obtained. The peel strength generally increases with time to a maximum (ultimate) value and the ultimate peel strength as used herein represents the adhesion value obtained for the metal layer greater than 3 days after metallization.
EXAMPLE II
EXAMPLE I was repeated except that the etched board was treated with ACTANE 70 prior to step (g) and a smooth adhesive coating was obtained.
EXAMPLE III
The procedure of EXAMPLE I was repeated except that a swellant composition containing, by volume, 25% N-methylpyrrolidone and 75% PGMME was used in step (a) instead of the DMSO composition and immersed for 10 minutes instead of 5. An ultimate peel strength of greater than 10 lbs/in was obtained.
EXAMPLE IV
Step (a) of EXAMPLE I was repeated using 100% DMSO and the plaque's surface was attacked and unsuitable for further processing. Similar results were obtained when 100% N-methylpyrrolidone was used in Step (a).
It will be apparent that many changes and modifications of the several features described herein
may be made without departing from the spirit and scope of the invention. It is therefore apparent that the foregoing description is by way of illustration of the invention rather than limitation of the invention.
Claims (8)
1. A method for improving the adhesive properties of a polyetherimide resin comprising:
(a) conditioning the resin by contacting the resin with a swellant compositon comprising a solution of a polar material having a dielectric constant greater than about 15 and a dipole moment greater than about 3 Debye Units and an organic solvent at an elevated temperature for a sufficent time to render the resin receptive to an etching process; and
(b) contacting the conditioned resin with an etchant composition comprising chromium ions at an elevated temperature above about 70°C. for a sufficent time to promote adhesion of metal plating on the plastic.
2. The method of claim 1 wherein the plastic is glass -filled polyetherimide.
3. The method of claim 2 wherein the swellant composition comprises a polar material selected from the group consisting of dim ethylsulf oxide; dimethylformamide; N-methylpyrrolidone; and mixtures thereof and the organic solvent is a polyhydric compound.
4. The method of claim 3 wherein the etchant composition comprises Crθ3 or Cr207 ions and H2S04.
5. The method of claim 3 wherein the polar material is N-methylpyrrolidone and the organic solvent is propylene glycol monomethyl ether.
6. The method of claim 3 wherein the polar material is dimethylsulfoxide and the organic solvent is propylene glycol monomethyl ether.
7. A polyetherimide resin product prepared in 5 accordance with the method of claim 1.
8. In a method for producing a metal coating on a pol etherimide resin substrate which comprises sensitizing and activating the surface of the resin and lOelect rolessly coating a metal thereon followed, optionally, by electroplating, the improvement for increasing the adhesiveness of the metal coating on the resin substrate comprising:
15 (a) conditioning the resin by contacting the resin with a . swellant composition comprising a mixture of a polar material having a dielectric 'constant greater than about 15 and a dipole moment greater than about 3 Debye Units and an organic
20 solvent at an elevated temperature for a sufficent time to render the resin receptive to an etching process; and
(b) contacting the conditioned resin with an etchant composition comprising chromium ions at an
25 elevated temperature above about 70°C. for a sufficient time to promote adhesion of metal plating on the resin.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US74811985A | 1985-06-24 | 1985-06-24 | |
| PCT/US1986/001199 WO1987000391A1 (en) | 1985-06-24 | 1986-05-28 | Process for conditioning the surface of plastic substrates prior to metal plating |
| US748119 | 1991-08-21 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU5991486A AU5991486A (en) | 1987-01-30 |
| AU580433B2 true AU580433B2 (en) | 1989-01-12 |
Family
ID=25008108
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU59914/86A Ceased AU580433B2 (en) | 1985-06-24 | 1986-05-28 | Process for conditioning the surface of plastic substrates prior to metal plating |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP0227746A4 (en) |
| JP (1) | JPS63500249A (en) |
| KR (1) | KR880700620A (en) |
| AU (1) | AU580433B2 (en) |
| BR (1) | BR8606709A (en) |
| CA (1) | CA1249188A (en) |
| ES (1) | ES8800992A1 (en) |
| IL (1) | IL79044A0 (en) |
| WO (1) | WO1987000391A1 (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4846929A (en) * | 1988-07-13 | 1989-07-11 | Ibm Corporation | Wet etching of thermally or chemically cured polyimide |
| US4941940A (en) * | 1988-11-07 | 1990-07-17 | Jp Laboratories, Inc. | Pre-swelling and etching of plastics for plating |
| US5049230A (en) * | 1988-11-07 | 1991-09-17 | Jp Laboratories, Inc. | Single step pre-swelling and etching of plastics for plating |
| US5015329A (en) * | 1988-11-07 | 1991-05-14 | Jp Laboratories, Inc. | Pre-swelling and etching of plastics for plating |
| US4999251A (en) * | 1989-04-03 | 1991-03-12 | General Electric Company | Method for treating polyetherimide substrates and articles obtained therefrom |
| DE3922477A1 (en) * | 1989-07-06 | 1991-01-17 | Schering Ag | SOURCING AGENT FOR PRE-TREATING SYNTHETIC RESIN BEFORE ELECTRICIZED METALIZATION |
| US5183552A (en) * | 1989-09-14 | 1993-02-02 | Schering Aktiengesellschaft | Process for metallization of a nonconductor surface, especially on a circuit board having preexisting copper surfaces |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4171240A (en) * | 1978-04-26 | 1979-10-16 | Western Electric Company, Inc. | Method of removing a cured epoxy from a metal surface |
| US4385084A (en) * | 1979-05-17 | 1983-05-24 | Nitto Electric Industrial Co., Ltd. | Process for preparing a selective permeable membrane |
| US4424095A (en) * | 1981-01-12 | 1984-01-03 | Kollmorgen Technologies Corporation | Radiation stress relieving of polymer articles |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5333628B1 (en) * | 1969-09-05 | 1978-09-14 | ||
| US3808028A (en) * | 1971-08-11 | 1974-04-30 | Western Electric Co | Method of improving adhesive properties of a surface comprising a cured epoxy |
| US3758332A (en) * | 1971-08-20 | 1973-09-11 | Western Electric Co | Method of metal coating an epoxy surface |
| US3790400A (en) * | 1972-07-24 | 1974-02-05 | Macdermid Inc | Preparation of plastic substrates for electroless plating and solutions therefor |
| JPS5584330A (en) * | 1978-12-22 | 1980-06-25 | Teijin Chem Ltd | Plating of polycarbonate resin molded article |
| CA1162354A (en) * | 1981-09-30 | 1984-02-21 | John F. Fogarty | Process for electroless metal plating of a polysulfone substrate |
| JPS61252691A (en) * | 1985-05-02 | 1986-11-10 | キヤノン株式会社 | Manufacturing method of printed wiring board |
-
1986
- 1986-05-28 WO PCT/US1986/001199 patent/WO1987000391A1/en not_active Ceased
- 1986-05-28 KR KR870700155A patent/KR880700620A/en not_active Ceased
- 1986-05-28 BR BR8606709A patent/BR8606709A/en unknown
- 1986-05-28 EP EP19860903950 patent/EP0227746A4/en not_active Withdrawn
- 1986-05-28 AU AU59914/86A patent/AU580433B2/en not_active Ceased
- 1986-05-28 JP JP61503368A patent/JPS63500249A/en active Pending
- 1986-06-04 CA CA000510800A patent/CA1249188A/en not_active Expired
- 1986-06-05 IL IL79044A patent/IL79044A0/en unknown
- 1986-06-23 ES ES556423A patent/ES8800992A1/en not_active Expired
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4171240A (en) * | 1978-04-26 | 1979-10-16 | Western Electric Company, Inc. | Method of removing a cured epoxy from a metal surface |
| US4385084A (en) * | 1979-05-17 | 1983-05-24 | Nitto Electric Industrial Co., Ltd. | Process for preparing a selective permeable membrane |
| US4424095A (en) * | 1981-01-12 | 1984-01-03 | Kollmorgen Technologies Corporation | Radiation stress relieving of polymer articles |
Also Published As
| Publication number | Publication date |
|---|---|
| AU5991486A (en) | 1987-01-30 |
| EP0227746A4 (en) | 1987-10-06 |
| EP0227746A1 (en) | 1987-07-08 |
| KR880700620A (en) | 1988-03-15 |
| CA1249188A (en) | 1989-01-24 |
| ES556423A0 (en) | 1987-12-01 |
| JPS63500249A (en) | 1988-01-28 |
| IL79044A0 (en) | 1986-09-30 |
| ES8800992A1 (en) | 1987-12-01 |
| BR8606709A (en) | 1987-08-11 |
| WO1987000391A1 (en) | 1987-01-15 |
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