US3438805A - Chemical metallizing process - Google Patents
Chemical metallizing process Download PDFInfo
- Publication number
- US3438805A US3438805A US540517A US3438805DA US3438805A US 3438805 A US3438805 A US 3438805A US 540517 A US540517 A US 540517A US 3438805D A US3438805D A US 3438805DA US 3438805 A US3438805 A US 3438805A
- Authority
- US
- United States
- Prior art keywords
- metal
- substrate
- plating
- complex
- salt
- 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
- 238000000034 method Methods 0.000 title claims description 71
- 230000008569 process Effects 0.000 title description 9
- 239000000126 substance Substances 0.000 title description 6
- 229910052751 metal Inorganic materials 0.000 claims description 97
- 239000002184 metal Substances 0.000 claims description 97
- 239000000758 substrate Substances 0.000 claims description 85
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 64
- 150000003839 salts Chemical class 0.000 claims description 64
- 238000007747 plating Methods 0.000 claims description 60
- 229910001385 heavy metal Inorganic materials 0.000 claims description 38
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims description 32
- 238000010438 heat treatment Methods 0.000 claims description 17
- 230000000737 periodic effect Effects 0.000 claims description 15
- 239000007787 solid Substances 0.000 claims description 11
- 238000000354 decomposition reaction Methods 0.000 claims description 3
- 238000000576 coating method Methods 0.000 description 29
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 25
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 25
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
- 239000000243 solution Substances 0.000 description 24
- 239000000203 mixture Substances 0.000 description 23
- 239000002904 solvent Substances 0.000 description 23
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 22
- 229910052802 copper Inorganic materials 0.000 description 22
- 239000010949 copper Substances 0.000 description 22
- -1 ir-on Chemical compound 0.000 description 22
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- 239000000463 material Substances 0.000 description 7
- 238000001465 metallisation Methods 0.000 description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
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- 125000001183 hydrocarbyl group Chemical group 0.000 description 6
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- QQVIHTHCMHWDBS-UHFFFAOYSA-L isophthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC(C([O-])=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-L 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
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- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
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- 229910052753 mercury Inorganic materials 0.000 description 1
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- XVDBWWRIXBMVJV-UHFFFAOYSA-N n-[bis(dimethylamino)phosphanyl]-n-methylmethanamine Chemical compound CN(C)P(N(C)C)N(C)C XVDBWWRIXBMVJV-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- 125000005064 octadecenyl group Chemical group C(=CCCCCCCCCCCCCCCCC)* 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 229910052762 osmium Inorganic materials 0.000 description 1
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
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- SDKPSXWGRWWLKR-UHFFFAOYSA-M sodium;9,10-dioxoanthracene-1-sulfonate Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2S(=O)(=O)[O-] SDKPSXWGRWWLKR-UHFFFAOYSA-M 0.000 description 1
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- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
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- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
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- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/08—Metals
-
- 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
Definitions
- This invention relates to a chemical metallizing process and more particularly to a method of chemically metallizing a substrate by heating a metal salt/phosphine complex in the presence of the substrate.
- Metal-coated articles are presently enjoying wide utility. They are often conveniently obtained by chemical or non-electrolytic methods, starting with a compound of the coating metal and converting it to the metal under controlled conditions. In general, however, the known methods are not entirely satisfactory; they each have one or more disadvantages such as requiring exceedingly high temperatures or preformed organometallic compounds, or are limited to aqueous plating baths or to the use of active metal substrates in accordance with the electro motive series, or are otherwise not readily adapted to plating a wide variety of substrates. Of particular interest at the present time is the coating of non-metallic substrates such as plastics.
- substrates can be chemically metallized by the process which comprises heating a metal salt/phosphine complex derived from one mole of a non-organometallic salt of a normally solid heavy metal of the Deming Periodic Table and about 1 to 4 moles of a triorgano phosphine in which each organo group is a hydrocarbyl or dihydrocarbylamino radical in the presence of the substrate to be metallized at a temperature of about 25 to 350 C., but below decomposition temperature of the substrate and the heavy metal salt alone, provided that when the substrate is not a heavy metal of the Deming Periodic Table other than the plating metal, the metal salt/phosphine complex is in substantially pure form in direct contact with the substrate.
- metallized metal-coated or metalimpregnated.
- normally solid heavy metals heavymetals which are solid at normal ambient temperatures, thereby excluding metals such as Hg and Ga which are liquid at temperatures as low as about 30 C.
- plating metal is meant the heavy metal of the salt from which the complex is derived.
- substantially pure form is meant undiluted by any substantial amount of solvent, diluent or carrier. Minor amounts of impurities and additives are readily tolerated.
- the substrate When the substrate is a normally solid heavy metal of the Deming Periodic Table other than the plating metal, the substrate may be immersed in a bath containing the metal salt/phosphine complex dissolved in an inert solvent and the bath is heated for a time sufiicient to provide an adherent coating of the plating metal on the substrate.
- the metal salt/phosphine complex is heated in substantially pure form in direct contact with the substrate.
- direct contact between the complex in substantially pure form and the substrate is required, it is most conveniently provided by coating the substrate with the complex alone, especially in the case of a liquid complex, or by mixing the complex with a volatile carrier such as a solvent or diluent, coating the substrate with the mixture, evaporating the volatile carrier and heating the coated substrate thereby metallizing the substrate.
- metal impregnates as well as coatings can be produced with a wide variety of polymeric substrates that are also soluble in such solvents and can be recovered and reconstituted by solvent evaporation.
- a substrate such as plastic
- the metal salt/phosphine complex and a soluble polymer are dissolved in a mutual inert volatile solvent, the solvent is evaporated to form an intimate metal salt/phosphinepolymer mixture which is heated to produce the impregnated plastic.
- a solvent is chosen which softens, swells or dissolves the plastic substrate thereby allowing the plating components to penetrate the surface or to become completely and intimately associated therewith.
- Solutions of the metal salt/phosphine complex and the substrate polymer can be cast as films, spun into fibers or molded into any desired shape and, with evaporation of the solvent and heating, converted into a metallized product.
- the method of this invention comprises heating the metal salt/phosphine complex in the presence of the substrate to be metallized at the temperature required to etfect the metal salt/phosphine to metal transformation in the particular case.
- the required temperature which may be as high as 350 C., but usually is in the range of 25 to 250 C., is significantly lower than that required to decompose the metal salt alone to the free metal.
- plating temperatures generally range from about 25 to 150 C.
- the substrate is other than the specified heavy metals, somewhat higher temperatures in the range of about to 250 C. are generally required.
- metal plating with the same metal salt/ phosphine complex may require diiferent temperatures depending upon whether or not the substrate is one of the specified heavy metals.
- any of the heavy metals can be plated on any other heavy metal at substantially reduced temperatures.
- the complexes used in accordance with this invention are derived in part from salts of the normally solid heavy metals of the Deming Periodic Table. These heavy metals are defined in the Deming Periodic Table as shown by H. G. Deming in Fundamental Chemistry, 2nd edition (1947), page 255, John Wiley & Sons, Inc. and by Lange in Handbook of Chemistry, 10th Edition, pages 56 and 57.
- Suitable heavy metals which may be used in accordance with this invention include: Cu, Ag and Au (Group I-B); Zn and Cd (Group II-B); Al, T1 and In (Group III); Sn, Pb, Ti and Zr (Group IV); Sb, V, Nb, Ta and Bi (Group V); Cr, Mo and W (Group VI); Mn and Re (Group VII); Fe, Ru, Co, Rh, Ni, Pd, Pt, Os and Ir (Group VIII).
- the heavy metal salts from which the metal salt/ phosphine complexes are derived are non-organometallic salts.
- non-organometallic salt is meant a salt which is free of carbon-metal bonds.
- this invention is directed to the utilization of heavy metal compounds in their commonly available essentially organic salt forms and does not require that the metal salts first be activated by conversion to an intermediary organometallic form.
- the heavy metals are commonly available and conveniently used as the chlorides, bromides, iodides, cyanides, nitrites, nitrates, perchlorates, fluoroborates, carbonates or carboxylates such as acetates and trifiuoroacetates.
- Preferred plating metals are the ductile, noble and precious metals of Groups LB, and VIII, especially the salts of silver, copper, gold, nickel, cobalt, palladium and platinum. Still other preferred plating metals are titanium, chromium, zinc and tin. These are preferably employed as the readily available chlorides, bromides and iodides, but sometimes, as in the case of silver, are more advantageously used as the nitrites, nitrates or perchlorates.
- the complexes are also derived in part from triorgano phospines in which each organo group is a hydrocarbyl or dihydrocarbylamino radical.
- each organo group is a hydrocarbyl or dihydrocarbylamino radical.
- Each of the hydrocarbyl groups including those in the dihydrocarbylamino radical, may he aliphatic, cycloaliphatic or aromatic and, for reasons of availability and economy, normally contain from about 1 to 10 carbon atoms, but may contain up to about 18 carbon atoms.
- These groups may be straightchain, branched-chain, saturated or unsaturated including ethylenic and acetylenic unsaturation.
- Exemplifying such groups are methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, amyl, hexyl, octyl, decyl, dodecyl, hexadecyl, octadecyl, propenyl, allyl, butenyl, propargyl, octadecenyl, cyclopentyl, cyclohexyl, cyclohexenyl, phenyl, tolyl, xylyl, ethylphenyl, styryl and dodecylphenyl.
- the trialkyl phosphines are preferred, particularly the trilower alkyl phosphines having from about 1 to carbon atoms in each alkyl group.
- hydrocarbyl secondary amino groups are preferably, for reasons of availability and economy, di-lower alkylamino groups where each alkyl has from about 1 to 5 carbon atoms such as dimethylamino, diethylamino, methylethylamino, dibutylamino, methyl amylamino and diamylamino.
- Suitable homologs and analogs include dioctylamino, methyl octadecylamino, ethyloctadecenylamino, methyl cyclopentylamino, methyl cyclohexylamino, octyl cyclohexylamino, dicyclohexylamino, N- methylanilino, N-ethylanilino and N-methyl toluidino.
- the hydrocarbyl group may also constitute a single divalent radical such as the pyrrolidino and piperidino radicals.
- the process of this invention may be carried out using a preformed metal salt/phosphine complex, or the complex may be prepared in situ by adding the metal salt and phosphine separately to a solvent in which the complex is soluble. In either case, the complex is formed and acts as a necessary component in the process. When the complex is formed in situ small excesses of metal salt or phosphine may be present. These do not interfere with the metallization process.
- phosphines and heavy metal salts generally form definite coordination complexes involving from 1 to 4 moles of the phosphine per mole of the salt.
- the phosphine is normally present in amounts corresponding to at least about one mole per mole of heavy metal salt. More than about four moles of the phosphine per mole of salt is generally not needed, but may be used, if desired. The optimum amount of the phosphine may vary depending on the particular heavy metal salt and the substrate to be coated.
- the metal salt/phosphine complexes decompose to form metal at or slightly above their melting points and in general this is completed at temperatures below about 350 C.
- the triaryl phosphine complexes are thermally more stable than the trialkyl phosphine complexes and require higher metallization temperatures. This may be advantageously used where enhanced thermal stability of a complex is needed as in controlled and step-Wise metal deposition.
- the wide variety of phosphines that are available enables one to control or vary the temperature of metallization to suit the particular processing need.
- the metal salt/phosphine complexes in contrast to the metal salts from which they are derived, are highly soluble in a wide variety of organic solvents making possible the formulation of a wide range of plating compositions.
- the solvent of course should be substantially inert to the plating ingredients and the substrate.
- Suitable solvents include alcohols such as methanol, ethanol, 2- propanol and 2-methyl-1-propanol; ethers such as diethyl ether, furan, tetrahydrofuran and dioxane; ketones such as acetone and methyl ethyl ketone; hydrocarbons such as pentane, hexane, isooctane, tetradecane, benzene, xylene and toluene; halogenated hydrocarbons such as chloroform, methylene chloride, carbon tetrachloride, chlorobenzene, dichlorobenzene, trichloroethylene, 1,1, 2,2 tetrachloro-1,2-difiuoroethane, l,1,2-trichloro-1,2,2- trifluoroethane, trichlorofluoromethane, chlorotrifiuoromethane and mixtures and azeotropes thereof;
- the main function of the solvent is to provide liquid, easily handled compositions which can effectively bring the metal salt/phosphine complex in intimate contact with the substrate to be metallized.
- the solvent may also serve to transfer heat to the metallizing components and as a vehicle for other ingredients having beneficial effects such as plating promoters and surface conditioners. Volatile solvents are preferred, particularly those which can be evaporated from the metallizing compositions at temperatures at or below the temperature at which metallization occurs.
- the method of this invention can be applied to a wide variety of substrates, including metallic and non-metallic materials.
- the metals may be any of those normally used for decorative, structural or electrical purposes. These are usually the normally solid heavy metals of the Deming Periodic Table and alloys thereof. For practical reasons the substrate metal is generally different from the plating metal except where special elfects such as relief are desired. Besides the heavy metals, other metals may also serve as substrates including the rare earths such as cerium and actinides such as uranium. As pointed out above the substrate metal may be higher or lower than the plating metal in the electromotive series of the metals.
- siliceous solids such as glass, Pyrex glass, spun glass, and asbestos
- carbonaceous materials such as graphite and the various amorphous carbon blacks
- refractory materials such as Carborundum, ceramics and cermets
- natural and synthetic cellulosic materials such as cotton, hemp, jute, paper, parchment, wood, cellulose acetate, and rayon
- proteinous materials such as silk, wool, leather, mohair and fur.
- Still other important substrates are the synthetic polymeric compositions exemplified by the polyvinyls such as polyacrylonitrile, polyvinyl chloride, polytrifiuorochloroethylene, polytetrafiuoroethylene, polystyrene, polyethylene, polypropylene, polyvinyl acetate, polyvinylidene fiuoride, poly(alkyl methacrylates) and copolymers thereof; polybutadiene, poly(diallyl esters) such as poly(diallyl phthalate); polyamides such as nylon, polyimides, polyesters, polyurethanes, polyacetals, melamine-formaldehyde, urea-formaldehyde, phenol-formaldehyde and epoxies.
- the metallization temperature should be below the deformation temperature of the polymer.
- the substrate may be particulate, for example powdered, or it may have a continuous surface in the form of a sheet, film, tape, foil, wire, fiber, fabric or foam. It may be a highly surface porous mass which is to be impregnated and coated at the same time such as a porous catalyst support.
- the substrate to be plated should be clean especially with respect to grease and loose scale.
- Any of the known techniques may be used to prepare the surface to be plated.
- metal surfaces can be treated as described by Burns and Bradley in Protective Coatings for Metals, 2nd Edition, Chapter 2, Reinhold Publishing Corporation.
- Plastic surfaces can also be preconditioned according to known techniques.
- the surface can be mechanically satinized as described by Bruner and Baranano in Modern Plastics, December 1961, and in Chemical and Engineering News, Mar, 25, 1963, pages 48 and 49.
- the surfaces may be chemically etched, as in the case of polyfluoroethylene being treated with an alkali metal-amine solution as described in Canadian Patent No. 653,304, or with an alkali metal-aromatic ether solution as described in US. Patent No. 2,809,130.
- conditioners such as the commonly employed hydrohalic acids including hydrochloric, hydrobromic, hydrofluoric and hydroiodic acids or sulfuric acid, or by treating with a small amount of an inorganic reducing salt such as stannous chloride.
- conditioners such as the commonly employed hydrohalic acids including hydrochloric, hydrobromic, hydrofluoric and hydroiodic acids or sulfuric acid, or by treating with a small amount of an inorganic reducing salt such as stannous chloride.
- Such promoters may be incorporated directly into the metal salt/phosphine plating composition of this invention, if desired. Conveniently this may be done in a carrier solvent, especially alcohols such as methyl, ethyl and propyl alcohols.
- the temperature or time required for metallization in accordance with this invention can be further reduced by sensitizing the metal salt/ phosphine complex to subsequent thermal treatment.
- Sensitization may be accomplished by incorporating into the metal salt/phosphine complex plating composition a thermally dissociable free radical generator such as carbon tetrabromide or an organic peroxide, or by irradiating the complex with ultraviolet light, or exposing it to an electron beam or contacting it with a spark discharge.
- the temperature requirement can be reduced by as much as 100 C, for plating on nonmetallic substrates.
- the sensitizing step is particularly advantageous in the case of heat sensitive substrates such as certain plastics. This improvement allows the use of a wider variety of complexes with these substrates.
- Examples 16 to 25 The procedure of Examples 1-15 was repeated with a solution containing 1 part of (CH P-AuCl, 200 parts of methanol and 3 parts of concentrated hydrochloric acid to produce adherent gold plates on various metal substrates at 60 C. and the time indicated in the table below.
- Example 27 The procedure of Example 26 was repeated using 200 mesh powdered nickel as the substrate 'with the same result.
- Example 28 The procedure of Example 26 was repeated using 200 mesh powdered stainless steel as the substrate with the same result.
- Example 29 A plating solution containing 1 part of (CH P-AuCl, 200 parts of ethanol and 3 parts of concentrated hydrochloric acid was prepared. A 316 stainless steel coupon was placed in the solution for 2 hours at boiling. An adherent gold coating was produced on the 316 stainless steel.
- Example 30 The procedure of Example 29 was repeated except that 200 parts of 2-propanol were substituted for the ethanol with the same result.
- Example 31 The procedure of Example 29 was repeated except that 200 parts of 2-methyl1-propanol were substituted for the ethanol with the same result.
- Example 32 The procedure of Example 29 was repeated except that 200 parts of acetone were substituted for the ethanol with the same result.
- Example 33 The procedure of Example 29 was repeated except that 200 parts of chloroform were substituted for the ethanol with the same result.
- Example 42 Silver-plating compositions, prepared by dissolving 1 part of (CH P-AgI in 250 parts of 2-propanol, and adding 0.5 part of concentrated hydrochloric acid, produced lustrous, adherent silver plates on brass coupons immersed in the boiling solution for 0.5 hour.
- Example 43 The procedure of Example 42 was repeated using 250 parts of triethylamine in place of the 2-propanol with the same result.
- Example 44 The procedure of Example 42 was repeated using 250 parts of acetone in place of the 2-propanol with the same result.
- Example 45 The procedure of Example 42 was repeated using 25 0 parts of acetonitrile in place of the 2-propanol with the same result.
- Examples 52 to 55 Various copper salt/phosphine complexes were used in the procedure of Examples 1 to 15 to produce lustrous, adherent copper plates on various substrates under the conditions indicated in the table below.
- Example 5 6 The liquid complex, (C H PAu'Cl, was spread on a silicon wafer which was then heated on a 180 C. hot plate. Within 5 minutes, the Wafer had become coated with an adherent, electrically conductive gold layer. When cooled, the resistance of the wafer was less than 0.5 ohm/cm. or less than of the original resistance.
- Example 57 A 0.1% solution of (CH P-AgNO in acetone was spread over a 1 in. x 1 in. film of polytetrafluoroethyleue whose surface previously had been treated with a sodiumnaphthalene-te'trahydrofuran solution essentially as disclosed in US. Patent No. 2,809,120. After the acetone had evaporated, the film was placed with the coated side up on a 100 C. hot plate while the coated side was simultaneously heated with a hot air stream from a commercial hair dryer at a somewhat lower temperature. A bright silver coating appeared almost immediately.
- the silver coating was flexible, adherent, had a resistance of about 10 ohm/cmfi, and could be wiped with a paper towel to a mirror bright finish. Rubbing and compressing the coating with a spatula further improved its luster and conductivity.
- Example 5 8 Example 57 was repeated on a film of Delrin polyacetal resin that had previously been satinized as described by Bruner and Baranano in Modern Plastics, December 1961. Simply heating on a hot plate at C. for 15 minutes produced a lustrous, flexible, adherent and electrically-conductive silver coating on the film.
- Example 59 The procedure of Example 58 was repeated except that an untreated Zytel polyamide resin film was used as the substrate with essentially the same result.
- Example 70 Aluminum was plated on copper by heating a copper test coupon at 35 C. for 6 hours in a plating solution
- Example 60 prepared by adding 20 g. of triphenylphosphine (0.076 The procedure of Example 58 was repeated except that mole) in 100 ml. of ether to a filtered solution containing 5 g. of anhydrous -AlCl (0.038 mole) in 100 ml. of ether an untreated Mylar polyester film was used as the sub d Strata with essfinfiany the same result an removing the small amount of 011 that separated.
- Example 5 8 The procedure of Example 5 8 was repeated except that Thanipm was plated on 9 by heating a copper test an untreated Kapton type H polyimide film was used as coupon m a solution contanilng T1OC(O)CH3 the substrate with essentially the same result (0'01 11.1016) and of.tr.lbutylphosphme (0'02 mole) mole) in 50 m1. of acetonitrile for 3 hours at 80 C.
- Example 62 A solution containing 1 part of (CH C*H P-AgNO 1 part of a film-forming vinylidene fluoride/tetrafluoro- Infimm was heavlly ileposlted a g l coupon y ethylene copolymer and 4 parts of acetone was cast as a heating the gold coupon 1n a solut1o n conta1n1ng 2.2 g. of film on aluminum foil. The acetone was evaporated and 20 Incls H1016) and f trlb ylph phu le (0.04 the coated piece heated at 180 C.
- Example 73 The Procedure of Examplfi 62 was repeated except h A lustrous and adherent tin coating was obtained on a glass plate was used in place of the aluminum foil with copper by heating a copper test coupon for 2 hours at the same result. The metal-impregnated coating adhered 0 in a plating Solution Prepared by mixing 1 part to the glass. each of SnCl -2H O and (C H P in about 10 parts of Example 64 methanol.
- Such metallized polyimide structures are particularly useful for preparing mirrors, automotive interior hardware, printed circuits and battery electrodes.
- Example 106 A CH P -AuCl /polyacrylontrile/dimethylformamide solution, substantially as described in Example 105, was spread on a glass slide and the dimethylformamide evaporated by warming under a heat lamp. The resulting film was then covered with a stencil, irradiated with high intensity light by contact flashing with a 200 watt-second xenon flash tube (Hico lite, Model K; one millisecond duration fiash), then heated at C. for about 5 minutes. The resulting slide showed a lustrous, electrically conductive, adherent golden image corresponding to the irradiated areas.
- Example 107 Example was repeated with 1 part of (CH3 3P per 5 parts of poly[4,4'(hexafluoroisopropylidene)diphenol isophthalate] polyester as the carrier substrate in 100 parts of methylene chloride. The resulting film, after having been exposed to the spark discharge and heated at 200 C. for 2 minutes, was golden, adherent and electrically conductive.
- Such products are useful in printed circuitry for use at elevated temperatures.
- Example 108 The procedure of Example 107 was repeated except that a piece of porcelain was used in place of the glass slide with substantially the same result.
- Example 109 The procedure of Example 107 was repeated except that a piece of wood was used in place of the glass slide with substantially the same result.
- Example 110 The procedure of Example 107 was repeated except that a carbon sheet was used in place of the glass slide with substantially the same result.
- Example 1 1 1 The procedure of Example 107 was repeated except that a piece of ceramic was used in place of the glass slide with substantially the same result.
- Example 1 12 Repeating Example 107 with 0.5 part of the gold complex produced uniformly colored purple slides, indicating colloidal gold dispersed throughout the polymeric film, which were useful as interference filters.
- Example 1 13 A mixture of 1 part of (CH P-AgNO and 70 parts of film-forming polyvinylchloride, cast as a film on glass from dimethylformamide solution, was irradiated 3 times through a stencil with the light source described in Example 1-06 and then heated to 180 C. for 5 minutes to develop a silvery image. The silver deposit was much less noticeable in the unirradiated area.
- Example 114 The procedure of Example 113 was repeated except that 1 part of (C H P-AgClO was used as the silver complex with the same result.
- Example 115 The procedure of Example 113 was repeated except that 1 part of (C H P-AgOC()CH was used as the silver complex with the same result.
- Example 116 The procedure of Example 113 was repeated except that 1 part of (C H P-AgI was used as the silver complex with the same result.
- Example 117 The procedure of Example 113 was repeated except that 1 part of (C H P-AgOC(O)CF was used as the silver complex with the same result.
- Example 1 18 The procedure of Example 113 was repeated except that 1 part of [(CgH P] -Ag CO' was used as the silver complex with the same result.
- Example 119 The procedure of Example 113 was repeated except that 1 part of (C H P-AgCN was used as the silver complex with the same result.
- Example 120 The procedure of Example 113 was repeated except that 1 part of (C H P-AgNO was used as the silver complex with the same result.
- Example 121 metallized objects having continuous, adherent and, where needed, flexible, electrically conductive metal coatings.
- metallic coatings that protect the underlying material and that reflect light and infrared radiation
- electrically conductive articles such as printed circuits, resistors, capacitors, and electrodes for fuel cells and batteries
- various decorative pieces e.g. automotive hardware
- effects, and images based on the formation of metal surfaces (4) new catalyst structures wherein a catalytically active heavy metal is impregnated and coated on a porous substrate carrier; and (5) metallized films showing selective light transmission which can be used as optical filters.
- a method of chemically metalizing a substrate which comprises heating a metal salt/phosphjne complex derived from one mole of a non-organometallic salt of a normally solid heavy metal of the Deming Periodic Table and 1 .to 4 moles of a triorganophosph ine in which each organo group is a hydrocarbyl or dihydrocarbylamino radical in the presence of the substrate to be metallized at a temperature of 25 to 350 C., but below the decomposition temperature of the substrate and the metal salt alone, provided that when the substrate is not a heavy metal of the Deming Periodic Table other than the plating metal, the metal salt/phosphine complex is in substantially pure form in direct contact with the substrate.
- the substrate is a heavy metal other than the plating metal
- the metal salt/ phosph-ine complex is dissolved in an inert solvent and the temperature is 25 to 150 C.
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Description
United States Patent 3,438,805 CHEMICAL METALLIZING PROCESS Earl M. Potrafke, New Castle County, De]., assignor to E. I. du Pont de Nemours and Company, Wilmington, Del., a corporation of Delaware No Drawing. Filed Apr. 6, 1966, Ser. No. 540,517
Int. Cl. B44d 1/22 US. Cl. 117130 16 Claims This invention relates to a chemical metallizing process and more particularly to a method of chemically metallizing a substrate by heating a metal salt/phosphine complex in the presence of the substrate.
Metal-coated articles are presently enjoying wide utility. They are often conveniently obtained by chemical or non-electrolytic methods, starting with a compound of the coating metal and converting it to the metal under controlled conditions. In general, however, the known methods are not entirely satisfactory; they each have one or more disadvantages such as requiring exceedingly high temperatures or preformed organometallic compounds, or are limited to aqueous plating baths or to the use of active metal substrates in accordance with the electro motive series, or are otherwise not readily adapted to plating a wide variety of substrates. Of particular interest at the present time is the coating of non-metallic substrates such as plastics.
It is an object of this invention to provide a new chemical plating method utilizing readily available metal salts. Another object is to provide such a method which is not dependent on aqueous plating baths, or the activity of the metal substrate in accordance with the electromotive series. Still another object is to provide such a plating process for metallizing a wide variety of substrates, including non-metal as well as metal substrates. These and other objects will become apparent from the following description of the invention.
It has now been discovered that a wide variety of substrates can be chemically metallized by the process which comprises heating a metal salt/phosphine complex derived from one mole of a non-organometallic salt of a normally solid heavy metal of the Deming Periodic Table and about 1 to 4 moles of a triorgano phosphine in which each organo group is a hydrocarbyl or dihydrocarbylamino radical in the presence of the substrate to be metallized at a temperature of about 25 to 350 C., but below decomposition temperature of the substrate and the heavy metal salt alone, provided that when the substrate is not a heavy metal of the Deming Periodic Table other than the plating metal, the metal salt/phosphine complex is in substantially pure form in direct contact with the substrate. By metallized is meant metal-coated or metalimpregnated. By normally solid heavy metals is meant heavymetals which are solid at normal ambient temperatures, thereby excluding metals such as Hg and Ga which are liquid at temperatures as low as about 30 C. By plating metal is meant the heavy metal of the salt from which the complex is derived. By substantially pure form is meant undiluted by any substantial amount of solvent, diluent or carrier. Minor amounts of impurities and additives are readily tolerated.
When the substrate is a normally solid heavy metal of the Deming Periodic Table other than the plating metal, the substrate may be immersed in a bath containing the metal salt/phosphine complex dissolved in an inert solvent and the bath is heated for a time sufiicient to provide an adherent coating of the plating metal on the substrate.
When the substrate is not a heavy metal of the Deming Periodic Table other than the plating metal, the metal salt/phosphine complex is heated in substantially pure form in direct contact with the substrate. When direct contact between the complex in substantially pure form and the substrate is required, it is most conveniently provided by coating the substrate with the complex alone, especially in the case of a liquid complex, or by mixing the complex with a volatile carrier such as a solvent or diluent, coating the substrate with the mixture, evaporating the volatile carrier and heating the coated substrate thereby metallizing the substrate.
Because the metal salt-phosphine complexes are soluble in a wide variety of solvents, metal impregnates as well as coatings can be produced with a wide variety of polymeric substrates that are also soluble in such solvents and can be recovered and reconstituted by solvent evaporation. For impregnating a substrate such as plastic the metal salt/phosphine complex and a soluble polymer are dissolved in a mutual inert volatile solvent, the solvent is evaporated to form an intimate metal salt/phosphinepolymer mixture which is heated to produce the impregnated plastic. A solvent is chosen which softens, swells or dissolves the plastic substrate thereby allowing the plating components to penetrate the surface or to become completely and intimately associated therewith. Solutions of the metal salt/phosphine complex and the substrate polymer can be cast as films, spun into fibers or molded into any desired shape and, with evaporation of the solvent and heating, converted into a metallized product.
Broadly, the method of this invention comprises heating the metal salt/phosphine complex in the presence of the substrate to be metallized at the temperature required to etfect the metal salt/phosphine to metal transformation in the particular case. The required temperature, which may be as high as 350 C., but usually is in the range of 25 to 250 C., is significantly lower than that required to decompose the metal salt alone to the free metal.
When the substrate is a normally solid heavy metal of the Deming Periodic Table other than the plating metal, plating temperatures generally range from about 25 to 150 C. When the substrate is other than the specified heavy metals, somewhat higher temperatures in the range of about to 250 C. are generally required. In other words, metal plating with the same metal salt/ phosphine complex may require diiferent temperatures depending upon whether or not the substrate is one of the specified heavy metals.
While the exact nature of this phenomenon is not definitely known, it is believed that the specified heavy metals may enter into an exchange reaction with the heavy metal of the complex. Although it is not intended that this invention be limited to any particular theory, these exchange reactions could account for the lower temperatures encountered with heavy metal substrates.
However, these exchange reactions do not follow the normal relationships encountered in the electromotive series of the metals as shown for example by Lange in Handbook of Chemistry, 10th Edition, page 1218, Me- Graw-Hill Book Co. In accordance with this invention, metals such as aluminum, manganese, zinc, chromium, ir-on, cobalt, nickel and tin are readily plated on a substrate such as copper, which is lower down in the electromotive series than these plating metals. Such exchange reactions are contrary to the accepted rules of the electromotive series.
It is possible that the presence of the phosphine in the complex may alter the normal forces in the electromotive series. It has been found that by proper selection of the phosphine and solvent, any of the heavy metals can be plated on any other heavy metal at substantially reduced temperatures.
The complexes used in accordance with this invention are derived in part from salts of the normally solid heavy metals of the Deming Periodic Table. These heavy metals are defined in the Deming Periodic Table as shown by H. G. Deming in Fundamental Chemistry, 2nd edition (1947), page 255, John Wiley & Sons, Inc. and by Lange in Handbook of Chemistry, 10th Edition, pages 56 and 57. Suitable heavy metals which may be used in accordance with this invention include: Cu, Ag and Au (Group I-B); Zn and Cd (Group II-B); Al, T1 and In (Group III); Sn, Pb, Ti and Zr (Group IV); Sb, V, Nb, Ta and Bi (Group V); Cr, Mo and W (Group VI); Mn and Re (Group VII); Fe, Ru, Co, Rh, Ni, Pd, Pt, Os and Ir (Group VIII).
The heavy metal salts from which the metal salt/ phosphine complexes are derived are non-organometallic salts. By non-organometallic salt is meant a salt which is free of carbon-metal bonds. In other words, this invention is directed to the utilization of heavy metal compounds in their commonly available essentially organic salt forms and does not require that the metal salts first be activated by conversion to an intermediary organometallic form. The heavy metals are commonly available and conveniently used as the chlorides, bromides, iodides, cyanides, nitrites, nitrates, perchlorates, fluoroborates, carbonates or carboxylates such as acetates and trifiuoroacetates.
Preferred plating metals are the ductile, noble and precious metals of Groups LB, and VIII, especially the salts of silver, copper, gold, nickel, cobalt, palladium and platinum. Still other preferred plating metals are titanium, chromium, zinc and tin. These are preferably employed as the readily available chlorides, bromides and iodides, but sometimes, as in the case of silver, are more advantageously used as the nitrites, nitrates or perchlorates.
The complexes are also derived in part from triorgano phospines in which each organo group is a hydrocarbyl or dihydrocarbylamino radical. Each of the hydrocarbyl groups, including those in the dihydrocarbylamino radical, may he aliphatic, cycloaliphatic or aromatic and, for reasons of availability and economy, normally contain from about 1 to 10 carbon atoms, but may contain up to about 18 carbon atoms. These groups may be straightchain, branched-chain, saturated or unsaturated including ethylenic and acetylenic unsaturation. Exemplifying such groups are methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, amyl, hexyl, octyl, decyl, dodecyl, hexadecyl, octadecyl, propenyl, allyl, butenyl, propargyl, octadecenyl, cyclopentyl, cyclohexyl, cyclohexenyl, phenyl, tolyl, xylyl, ethylphenyl, styryl and dodecylphenyl. The trialkyl phosphines are preferred, particularly the trilower alkyl phosphines having from about 1 to carbon atoms in each alkyl group.
The hydrocarbyl secondary amino groups are preferably, for reasons of availability and economy, di-lower alkylamino groups where each alkyl has from about 1 to 5 carbon atoms such as dimethylamino, diethylamino, methylethylamino, dibutylamino, methyl amylamino and diamylamino. Suitable homologs and analogs include dioctylamino, methyl octadecylamino, ethyloctadecenylamino, methyl cyclopentylamino, methyl cyclohexylamino, octyl cyclohexylamino, dicyclohexylamino, N- methylanilino, N-ethylanilino and N-methyl toluidino. The hydrocarbyl group may also constitute a single divalent radical such as the pyrrolidino and piperidino radicals.
The process of this invention may be carried out using a preformed metal salt/phosphine complex, or the complex may be prepared in situ by adding the metal salt and phosphine separately to a solvent in which the complex is soluble. In either case, the complex is formed and acts as a necessary component in the process. When the complex is formed in situ small excesses of metal salt or phosphine may be present. These do not interfere with the metallization process.
As is Well known in the art, phosphines and heavy metal salts generally form definite coordination complexes involving from 1 to 4 moles of the phosphine per mole of the salt. For etiicient utilization of the heavy metal salt in forming the complex in situ, the phosphine is normally present in amounts corresponding to at least about one mole per mole of heavy metal salt. More than about four moles of the phosphine per mole of salt is generally not needed, but may be used, if desired. The optimum amount of the phosphine may vary depending on the particular heavy metal salt and the substrate to be coated. Usually, however, only about two moles of the phosphine are needed per mole of salt and sometimes only about one, particularly in the case of Group I-B metals. The formation of definite metal salt/phosphine complexes constitutes an important practical advantage since the complexes are easily obtained pure and can be conveniently stored and handled at ordinary temperatures.
In general the metal salt/phosphine complexes decompose to form metal at or slightly above their melting points and in general this is completed at temperatures below about 350 C. As a class, the triaryl phosphine complexes are thermally more stable than the trialkyl phosphine complexes and require higher metallization temperatures. This may be advantageously used where enhanced thermal stability of a complex is needed as in controlled and step-Wise metal deposition. Thus, the wide variety of phosphines that are available enables one to control or vary the temperature of metallization to suit the particular processing need.
The metal salt/phosphine complexes, in contrast to the metal salts from which they are derived, are highly soluble in a wide variety of organic solvents making possible the formulation of a wide range of plating compositions. The solvent of course should be substantially inert to the plating ingredients and the substrate. Suitable solvents include alcohols such as methanol, ethanol, 2- propanol and 2-methyl-1-propanol; ethers such as diethyl ether, furan, tetrahydrofuran and dioxane; ketones such as acetone and methyl ethyl ketone; hydrocarbons such as pentane, hexane, isooctane, tetradecane, benzene, xylene and toluene; halogenated hydrocarbons such as chloroform, methylene chloride, carbon tetrachloride, chlorobenzene, dichlorobenzene, trichloroethylene, 1,1, 2,2 tetrachloro-1,2-difiuoroethane, l,1,2-trichloro-1,2,2- trifluoroethane, trichlorofluoromethane, chlorotrifiuoromethane and mixtures and azeotropes thereof; nitriles such as acetonitrile, butyronitrile and benzonitrile; amines such as triethylamine, tributylamine, pyridine and picoline; amides such as dimethylformamide, dimethylacetamide, hexamethylphosphoramide and hexaethylphosphoramide; and esters such as ethyl acetate, butyl acetate and amyl acetate.
The main function of the solvent is to provide liquid, easily handled compositions which can effectively bring the metal salt/phosphine complex in intimate contact with the substrate to be metallized. The solvent may also serve to transfer heat to the metallizing components and as a vehicle for other ingredients having beneficial effects such as plating promoters and surface conditioners. Volatile solvents are preferred, particularly those which can be evaporated from the metallizing compositions at temperatures at or below the temperature at which metallization occurs.
The method of this invention can be applied to a wide variety of substrates, including metallic and non-metallic materials. The metals may be any of those normally used for decorative, structural or electrical purposes. These are usually the normally solid heavy metals of the Deming Periodic Table and alloys thereof. For practical reasons the substrate metal is generally different from the plating metal except where special elfects such as relief are desired. Besides the heavy metals, other metals may also serve as substrates including the rare earths such as cerium and actinides such as uranium. As pointed out above the substrate metal may be higher or lower than the plating metal in the electromotive series of the metals.
There may also be used as substrates siliceous solids such as glass, Pyrex glass, spun glass, and asbestos; carbonaceous materials such as graphite and the various amorphous carbon blacks; refractory materials such as Carborundum, ceramics and cermets; natural and synthetic cellulosic materials such as cotton, hemp, jute, paper, parchment, wood, cellulose acetate, and rayon; proteinous materials such as silk, wool, leather, mohair and fur. Still other important substrates are the synthetic polymeric compositions exemplified by the polyvinyls such as polyacrylonitrile, polyvinyl chloride, polytrifiuorochloroethylene, polytetrafiuoroethylene, polystyrene, polyethylene, polypropylene, polyvinyl acetate, polyvinylidene fiuoride, poly(alkyl methacrylates) and copolymers thereof; polybutadiene, poly(diallyl esters) such as poly(diallyl phthalate); polyamides such as nylon, polyimides, polyesters, polyurethanes, polyacetals, melamine-formaldehyde, urea-formaldehyde, phenol-formaldehyde and epoxies. When the substrate is a polymeric material, the metallization temperature should be below the deformation temperature of the polymer.
The substrate may be particulate, for example powdered, or it may have a continuous surface in the form of a sheet, film, tape, foil, wire, fiber, fabric or foam. It may be a highly surface porous mass which is to be impregnated and coated at the same time such as a porous catalyst support.
As is well known in the plating art, for best results the substrate to be plated should be clean especially with respect to grease and loose scale. Any of the known techniques may be used to prepare the surface to be plated. For example, metal surfaces can be treated as described by Burns and Bradley in Protective Coatings for Metals, 2nd Edition, Chapter 2, Reinhold Publishing Corporation. Plastic surfaces can also be preconditioned according to known techniques. For example, the surface can be mechanically satinized as described by Bruner and Baranano in Modern Plastics, December 1961, and in Chemical and Engineering News, Mar, 25, 1963, pages 48 and 49. Or the surfaces may be chemically etched, as in the case of polyfluoroethylene being treated with an alkali metal-amine solution as described in Canadian Patent No. 653,304, or with an alkali metal-aromatic ether solution as described in US. Patent No. 2,809,130.
It is often beneficial to condition the surfaces to be plated, especially metal surfaces, with conditioners such as the commonly employed hydrohalic acids including hydrochloric, hydrobromic, hydrofluoric and hydroiodic acids or sulfuric acid, or by treating with a small amount of an inorganic reducing salt such as stannous chloride. Such promoters may be incorporated directly into the metal salt/phosphine plating composition of this invention, if desired. Conveniently this may be done in a carrier solvent, especially alcohols such as methyl, ethyl and propyl alcohols.
As an improvement Within the scope of this invention, it has been discovered by other inventors that for many of the metal salt/phosphine complexes, especially those derived from the noble metals, the temperature or time required for metallization in accordance with this invention can be further reduced by sensitizing the metal salt/ phosphine complex to subsequent thermal treatment. Sensitization may be accomplished by incorporating into the metal salt/phosphine complex plating composition a thermally dissociable free radical generator such as carbon tetrabromide or an organic peroxide, or by irradiating the complex with ultraviolet light, or exposing it to an electron beam or contacting it with a spark discharge. By these techniques the temperature requirement can be reduced by as much as 100 C, for plating on nonmetallic substrates. The sensitizing step is particularly advantageous in the case of heat sensitive substrates such as certain plastics. This improvement allows the use of a wider variety of complexes with these substrates.
The following examples, illustrating the novel method disclosed herein for metallizing a wide variety of substrates, are given without any intention that the invention be limited thereto. In these examples, all parts and percentages are by weight unless otherwise specified; solutions of metal salt/phosphine complexes, where employed, were prepared and used in non-metallic (usually glass) containers; and metals to be plated were in the form of 1 in. x 1 in. x A; in. coupons unless otherwise noted. Preformed metal salt/phosphine complexes, where used, were prepared by known methods. Adherence of the metal coatings to the substrate was measured by the Scotch tape cross-hatch test.
(A) GROUP I-B PLATING Examples 1 to 15 A gold plating stock solution was prepared by dissolving 1 part of (CH P-AuCl in parts of ethanol containing 5 parts of added concentrated hydrochloric acid. Aliquots were used to plate immersed test coupons of various metals by heating at 80 C. for the time indicated in the table below.
TABLE I Substrate Example Time, hours Thallium- Tin 14 Tungsten After the plating treatment, the coupons were removed, washed with water, then acetone, and inspected. All had an adherent gold coating.
Examples 16 to 25 The procedure of Examples 1-15 was repeated with a solution containing 1 part of (CH P-AuCl, 200 parts of methanol and 3 parts of concentrated hydrochloric acid to produce adherent gold plates on various metal substrates at 60 C. and the time indicated in the table below.
TABLE II Substrate Example Time, hours 405 stainless steel 24. 410 stainless steel. 25 430 stainless steel Example 26 Example 27 The procedure of Example 26 was repeated using 200 mesh powdered nickel as the substrate 'with the same result.
Example 28 The procedure of Example 26 was repeated using 200 mesh powdered stainless steel as the substrate with the same result.
Example 29 A plating solution containing 1 part of (CH P-AuCl, 200 parts of ethanol and 3 parts of concentrated hydrochloric acid was prepared. A 316 stainless steel coupon was placed in the solution for 2 hours at boiling. An adherent gold coating was produced on the 316 stainless steel.
Example 30 The procedure of Example 29 was repeated except that 200 parts of 2-propanol were substituted for the ethanol with the same result.
Example 31 The procedure of Example 29 was repeated except that 200 parts of 2-methyl1-propanol were substituted for the ethanol with the same result.
Example 32 The procedure of Example 29 was repeated except that 200 parts of acetone were substituted for the ethanol with the same result.
Example 33 The procedure of Example 29 was repeated except that 200 parts of chloroform were substituted for the ethanol with the same result.
Examples 34 to 41 Using the procedure of Examples 1 to 15, various gold-plating compositions were used to adherently plate various metallic substrates under the conditions indicated in the table below.
TABLE III Exam- Plating Solution, parts Temp., Time, Substrate ple 0. hrs.
34 1 pt. (CH3)3P-A11Cl, 80 pts. 80 1 Bronze.
95% ethanol, 3 pts. cone. HBr.
35 1 pt. (C4HD)PA11CI, 250 pts. 80 6 Copper.
acetonitrile.
36. 1 pt. (CaHmP-AuCl, 100 pts. 100 0.1 Mild steel.
dirncthylformamidc, 20 pts. acetic acid.
37 1 pt. (GHmP'AuI, 160 pts. 60 0. Niobium.
methanol, 1 pt. conc. HF.
38 1 pt. (CHmRAuI, 160 pts. 60 1 Aluminum.
methanol, 1 pt. conc. HF.
39 1 pt. (CHa)aP-Au1, 160 pts. 60 1. 5 Uranium.
methanol, 1 pt. eonc. HF.
40 1 pt. (CHahP-AuI, 160 ts. 50 1.5 Aluminum.
acetone, 1 pt. cone. H
41 1 pt. (CeH5)3P-AIII, 250 pts. 80 Stainless 95 0 ethanol. steel.
Example 42 Silver-plating compositions, prepared by dissolving 1 part of (CH P-AgI in 250 parts of 2-propanol, and adding 0.5 part of concentrated hydrochloric acid, produced lustrous, adherent silver plates on brass coupons immersed in the boiling solution for 0.5 hour.
Example 43 The procedure of Example 42 was repeated using 250 parts of triethylamine in place of the 2-propanol with the same result.
Example 44 The procedure of Example 42 was repeated using 250 parts of acetone in place of the 2-propanol with the same result.
Example 45 The procedure of Example 42 was repeated using 25 0 parts of acetonitrile in place of the 2-propanol with the same result.
Examples 46 to 51 Various silver-plating compositions were used in the procedure of Examples 1 to 15 to produce lustrous adherent silver plates on various substrates under the conditions indicated in the table below.
TABLE IV Exam- Plating Composition, parts Temp., Time, Substrate ple 0. hrs.
46 1 pt. (CH3) P-AgI, 20 pts. 50 2. 5 Phosphor acetone. bronze. 47 1 pt. (CH P-AgI, 16 pts. 50 3 Copper (200 acetone. mesh) powder. 48 1 pt. [(CeHmPh-AgNo 1 Everdur" 16 pts. methanol. Cnu-Si-Mn a 0y. 49 1 pt. [(CBH5)2CH3P]4-ANO3, 80 0.2 Copper.
40 pts. acetonitrile. 50 1 pt. (CHmP-AgNOz, 40 pts. 80 0. 2 Do.
acetonitrile. 51 1 pt. (CoHrOaP-AgNOz, 80 O. 2 D0.
pts. acetonitrile.
Examples 52 to 55 Various copper salt/phosphine complexes were used in the procedure of Examples 1 to 15 to produce lustrous, adherent copper plates on various substrates under the conditions indicated in the table below.
TABLE V Exam- Plating Solution, parts Temp., Time, Substrate ple 0. hrs.
52 1 pt. [(CeH5)3P]2-C11Clz, 100 0.3 Mild steel.
100 pts. dimethylionnamide, 20 pts. acetic acid. 53 1 pt. [(CiHt)sP]z-CuC1z, 60 2 Cast iron.
30 pts. methanol, 0.05 pt. cone. HCl. 54 1 pt. [(C4H P]z'Cl1Clz, 80 2 Brass.
100 pts. 95% ethanol, 5 pts. cone. H01. 55 1 pt. (C4Hn)aP-CI1OC(O)CH 80 3 Gold.
100 pts. acetonitrile.
Example 5 6 The liquid complex, (C H PAu'Cl, was spread on a silicon wafer which was then heated on a 180 C. hot plate. Within 5 minutes, the Wafer had become coated with an adherent, electrically conductive gold layer. When cooled, the resistance of the wafer was less than 0.5 ohm/cm. or less than of the original resistance.
It will be apparent to those skilled in the solid state electronics art that this process and the gold-coated silicon produced thereby are useful for preparing integrated microcircuits.
Example 57 A 0.1% solution of (CH P-AgNO in acetone was spread over a 1 in. x 1 in. film of polytetrafluoroethyleue whose surface previously had been treated with a sodiumnaphthalene-te'trahydrofuran solution essentially as disclosed in US. Patent No. 2,809,120. After the acetone had evaporated, the film was placed with the coated side up on a 100 C. hot plate while the coated side was simultaneously heated with a hot air stream from a commercial hair dryer at a somewhat lower temperature. A bright silver coating appeared almost immediately. The silver coating was flexible, adherent, had a resistance of about 10 ohm/cmfi, and could be wiped with a paper towel to a mirror bright finish. Rubbing and compressing the coating with a spatula further improved its luster and conductivity.
Example 5 8 Example 57 was repeated on a film of Delrin polyacetal resin that had previously been satinized as described by Bruner and Baranano in Modern Plastics, December 1961. Simply heating on a hot plate at C. for 15 minutes produced a lustrous, flexible, adherent and electrically-conductive silver coating on the film.
9 Example 59 The procedure of Example 58 was repeated except that an untreated Zytel polyamide resin film was used as the substrate with essentially the same result.
1 (C) PLATING WITH GROUP III METALS Example 70 Aluminum was plated on copper by heating a copper test coupon at 35 C. for 6 hours in a plating solution Example 60 prepared by adding 20 g. of triphenylphosphine (0.076 The procedure of Example 58 was repeated except that mole) in 100 ml. of ether to a filtered solution containing 5 g. of anhydrous -AlCl (0.038 mole) in 100 ml. of ether an untreated Mylar polyester film was used as the sub d Strata with essfinfiany the same result an removing the small amount of 011 that separated.
Example The procedure of Example 5 8 was repeated except that Thanipm was plated on 9 by heating a copper test an untreated Kapton type H polyimide film was used as coupon m a solution contanilng T1OC(O)CH3 the substrate with essentially the same result (0'01 11.1016) and of.tr.lbutylphosphme (0'02 mole) mole) in 50 m1. of acetonitrile for 3 hours at 80 C. Example 62 Example 72 A solution containing 1 part of (CH C*H P-AgNO 1 part of a film-forming vinylidene fluoride/tetrafluoro- Infimm Was heavlly ileposlted a g l coupon y ethylene copolymer and 4 parts of acetone was cast as a heating the gold coupon 1n a solut1o n conta1n1ng 2.2 g. of film on aluminum foil. The acetone was evaporated and 20 Incls H1016) and f trlb ylph phu le (0.04 the coated piece heated at 180 C. for 5 minutes to demole) 111 50 1111- f aC t mtnle for 3 hours at 80 C. glellltgraufieitglle, silvery coating WhlCh was adherent to the (D) PLATING WITH GROUP IV METALS Example 63 Example 73 The Procedure of Examplfi 62 was repeated except h A lustrous and adherent tin coating was obtained on a glass plate was used in place of the aluminum foil with copper by heating a copper test coupon for 2 hours at the same result. The metal-impregnated coating adhered 0 in a plating Solution Prepared by mixing 1 part to the glass. each of SnCl -2H O and (C H P in about 10 parts of Example 64 methanol. The emission spectrum of the coating corre- A piece of Torvex ceramic honeycomb (4 in. in disponded to that Of metalliC t nameter, l in. thick and having a in. pore size) was Exam 1e 74 dipped into one liter of a 1% solution of (CH P-Ag N O P in acetonitrrle, air dried to evaporate the acetonitnle, The procedure of Example was repeated 6Xcept that 2 i g l f gtgl zg gf if) gvgl gg g gilz 6 ggti r l g a silver telst coupon was used 1n place of copper with the a PTOXlm same resu t. The procedure was repeated eight times to build up a Examples 75 to 81 continuous silver coating throughout the porous structure Metal plates were obtained by immersing a substrate in Such product, presenting a large silver surface, but with 40 a pl ti p s t on and heating for 1-6 hours under the its open honeycomb structure substantially unchanged so C0I1d1t10 I1 S Summarlled 1n the p belOW- T Plating that gas flowing through it remains substantially unimcomposltlons w P p v approxlmatqly peded, is useful as a silver catalyst in vapor phase reacmolar P P Of a P P e, a mo ar proportion of tions a Group IVB metal salt and optionally about 10 parts of a diluent per part of metal salt. Visual inspection and, (B) PLATING W1 r H GROUP H B METALS where taken, the X-ray fluorescence or emission spectrum Examples to 71 of each resulting test piece showed a Group IV-B metallic Metal coupons to be plated, 1 in. x 1.5 in. x A in., Coatmg on Its Surface were immersed in liquid plating compositions, consisting 50 TABLE VII of 1 part of a bis(trialkylphosphine) metal halide diluted with about 2.5 parts of an inert solvent as specified in 3 salt RBRR Smvent 3 6?" 53E; the table below. The coupons were held in the baths for 75 T01 B t 1 N 100 C the times and at the temperatures noted in the table be- 3 5 1 SQZHgfiffdffi": 40 E8 77 ..I"C1 -.d A t 't '1 100 D lstgvtergmoved, rinsed wlth water and acetone, and 1n 5 78 i g g fi g m0 i g f 91ml 6. S ee Yellow metal substrates were chosen for these tests 79 TiIB Dir l l et yleli aethylghos- 100 Copper. so that the formation of silvery-white metal coatings 80 Zrch g gif; would be readily apparent on visual inspection. All coat- 81 Zr012 gg g y y ormam- 100 Do. ings were adherent.
TABLE VI Example Plating Composition Tergll, Tfime, Substrate Result 65 [(OH P] -ZnBr +dimethyl- 100 0.5 Copper.-- Zn coating.
iormamide. 66 [(C4H )3P]2-Zu(OC(O)CH3)2 25 24 Brass Do.
plus dimethyltormamide. 67 [((CH3)2N)3P]2-ZI1Clzp1llS 100 24 Copper.-- Heavy Zn hexamethylphosphoramide. coatmg. 68 [((CHa)2N)aP]2-ZI1I2 plus 100 24 d0 Do.
hexamethylphosphoramide. 69 [(C4H9)3P]2-Cd0lz plus 0.5 .do Lustrous tetradecane. 3
plating.
11 (E) PLATING WITH GROUP v METALS Examples 82 to 88- Metal plates were produced on copper test coupons with the plating compositions specified in the table below which were prepared as in Examples 75 to 81. Heating was 16 hours at 100 C. except in the case of Example 88 which was for 12 hours. Plating in Examples 82 to 84 was confirmed by X-ray emission and fluorescence spectra of the coatings.
(F) PLATING WITH GROUP VI METALS Examples 89 to '92 Metal plates were produced on copper test coupons with the plating compositions specified in the table below which were prepared as in Examples 75 to 81. Heating was 16 hours at 100 C. X-ray emission spectroscopy confirmed that the Example 91 plate was chromium.
TABLE IX Plating Composition Salt Pliosphine, R3P,R= Solvent CrCla Dimethylamino Dimethyltormamide. CrCla d Do. CrClz do Do. 92 MoCla do None.
(G) PLATING WITH GROUP VII METAL Example 93 Following the procedure of Examples 75 to 81, a manganese coating, confirmed by X-ray emission spectroscopy, was plated on copper by heating a test coupon in a [(CH P-MnCl hexamethylphosphoramide solution for 12 hours at 150 C.
(H) PLATING WITH GROUP VIII METALS Examples 94 to 103 The procedure followed was essentially that described for Examples 75 to 81, except that the plating compositions and conditions were varied as noted in the table below. In Example 94 the coating was confirmed by emission spectroscopy. In Examples 94 to 97, the salt and phosphine were separately added to the solvent; in Examples 98 to 103, the preformed complex MX -R P was added directly to the plating solvent. In all cases the coatings were adherent.
12 Example 104 About 1 g. of finely powdered [(CH P] -PdCl was spread on a 2 ml thick, 3 in. x 3 in. square of a high temperature resistant Kapton type H polyimide film. The coated film was gradually heated on a hot plate under a nitrogen atmosphere to about 350 C. until the complex had decomposed and had deposited on the film an adherent, lustrous, electrically-conductive palladium coating.
Such metallized polyimide structures are particularly useful for preparing mirrors, automotive interior hardware, printed circuits and battery electrodes.
(I) EXAMPLES I'LLUSTRATING IMPROVEMENTS WITHIN THE SCOPE OF THIS INVENTION Example 105 One part of (CH P-AuCl was dissolved in 25 parts of a 15% solution of Orlon polyacrylonitrile in dimethylformamide. The solution was spread on a glass microscope slide and warmed with a heat lamp to evaporate the dimethylformamide. The slide was then exposed to a Tesla coil spark discharge to sensitize the gold salt complex to thermal decomposition and placed treated-side up on a 200 C. hot plate for about 5 minutes. The resulting uniformly distributed golden coating was adherent to the glass and electrically conductive.
Example 106 A (CH P -AuCl /polyacrylontrile/dimethylformamide solution, substantially as described in Example 105, was spread on a glass slide and the dimethylformamide evaporated by warming under a heat lamp. The resulting film was then covered with a stencil, irradiated with high intensity light by contact flashing with a 200 watt-second xenon flash tube (Hico lite, Model K; one millisecond duration fiash), then heated at C. for about 5 minutes. The resulting slide showed a lustrous, electrically conductive, adherent golden image corresponding to the irradiated areas.
Example 107 Example was repeated with 1 part of (CH3 3P per 5 parts of poly[4,4'(hexafluoroisopropylidene)diphenol isophthalate] polyester as the carrier substrate in 100 parts of methylene chloride. The resulting film, after having been exposed to the spark discharge and heated at 200 C. for 2 minutes, was golden, adherent and electrically conductive.
Such products are useful in printed circuitry for use at elevated temperatures.
Example 108 The procedure of Example 107 was repeated except that a piece of porcelain was used in place of the glass slide with substantially the same result.
TABLE X Plating Composition Example Temp., Time, Sub- Result Salt Phosphtne Solvent 0. hrs. strate R3P,R=
Me N Hexamethyl- 12 Copper.. Fe coat.
phosphoramide. Butyl Acetonitrile 80 3 d0 Co coat. R MezN Hexamethyl- 150 12 do Rh coat.
phosphoramide. 97 NlBlg Phenyl 83% acetonitrlle, 17% 80 1 do Bright Ni acetic acid. coat. 98 N101: Butyl Acetic acid 100 3. 5 d0 Lustrous Ni coat; 99 NiBn do .d0 100 2 Bronze. Do. 100.. NlClz 95% ethanol plus 5% 70 2 Brass Ni coat.
cone. H01. do o 70 .1 do Lustrous Pd coat. 95% ethanol plus trace 70 7 Copper Lustrous HF. Pt coat. do -do 70 7 ..do Pt coat.
13 Example 109 The procedure of Example 107 was repeated except that a piece of wood was used in place of the glass slide with substantially the same result.
Example 110 The procedure of Example 107 was repeated except that a carbon sheet was used in place of the glass slide with substantially the same result.
Example 1 1 1 The procedure of Example 107 was repeated except that a piece of ceramic was used in place of the glass slide with substantially the same result.
Example 1 12 Repeating Example 107 with 0.5 part of the gold complex produced uniformly colored purple slides, indicating colloidal gold dispersed throughout the polymeric film, which were useful as interference filters.
Example 1 13 A mixture of 1 part of (CH P-AgNO and 70 parts of film-forming polyvinylchloride, cast as a film on glass from dimethylformamide solution, was irradiated 3 times through a stencil with the light source described in Example 1-06 and then heated to 180 C. for 5 minutes to develop a silvery image. The silver deposit was much less noticeable in the unirradiated area.
Example 114 The procedure of Example 113 was repeated except that 1 part of (C H P-AgClO was used as the silver complex with the same result.
Example 115 The procedure of Example 113 was repeated except that 1 part of (C H P-AgOC()CH was used as the silver complex with the same result.
Example 116 The procedure of Example 113 was repeated except that 1 part of (C H P-AgI was used as the silver complex with the same result.
Example 117 The procedure of Example 113 was repeated except that 1 part of (C H P-AgOC(O)CF was used as the silver complex with the same result.
Example 1 18 The procedure of Example 113 was repeated except that 1 part of [(CgH P] -Ag CO' was used as the silver complex with the same result.
Example 119 The procedure of Example 113 was repeated except that 1 part of (C H P-AgCN was used as the silver complex with the same result.
Example 120 The procedure of Example 113 was repeated except that 1 part of (C H P-AgNO was used as the silver complex with the same result.
Example 121 metallized objects having continuous, adherent and, where needed, flexible, electrically conductive metal coatings. For example, it is useful to produce (1) metallic coatings that protect the underlying material and that reflect light and infrared radiation; (2) electrically conductive articles such as printed circuits, resistors, capacitors, and electrodes for fuel cells and batteries; (3) various decorative pieces (e.g. automotive hardware); effects, and images based on the formation of metal surfaces; (4) new catalyst structures wherein a catalytically active heavy metal is impregnated and coated on a porous substrate carrier; and (5) metallized films showing selective light transmission which can be used as optical filters. It is also useful to obtain coatings of the normally brittle metals such as titanium, zirconium, chromium, vanadium, niobium, and manganese which are difiicult to obtain by other methods. It is also useful to produce metallized plastics wherein the metal is uniformly distributed throughout the body of the plastic as well as on its surface. This is of great practical advantage when the surface of the plastic is normally subjected to abrasion.
The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
1. A method of chemically metalizing a substrate which comprises heating a metal salt/phosphjne complex derived from one mole of a non-organometallic salt of a normally solid heavy metal of the Deming Periodic Table and 1 .to 4 moles of a triorganophosph ine in which each organo group is a hydrocarbyl or dihydrocarbylamino radical in the presence of the substrate to be metallized at a temperature of 25 to 350 C., but below the decomposition temperature of the substrate and the metal salt alone, provided that when the substrate is not a heavy metal of the Deming Periodic Table other than the plating metal, the metal salt/phosphine complex is in substantially pure form in direct contact with the substrate.
2. The method of claim 1 in which the substrate is a heavy metal other than the plating metal, the metal salt/ phosph-ine complex is dissolved in an inert solvent and the temperature is 25 to 150 C.
3. The method of claim 2 in which the complex is derived from a salt of a heavy metal of Group I-B or VIII of the Deming Periodic Table and a trialkylphosphine.
4. The method of claim 1 in which the substrate is not a heavy metal other than the plating metal.
5. The method of claim 4 in which a solution containing the metal salt/phosphi-ne complex in a volatile inert solvent is coated on the substrate, the solvent is evaporated, and the coated substrate is heated to metallize the surface.
6. The method of claim 5 in which the complex is derived from a salt of a heavy metal of Group I-B or VIIII of the Deming Periodic Table and a trialkylphosp me.
7. The method of claim 5 in which the temperature is to 350 C.
8. The method of claim 6 in which the complex is derived from gold chloride and a tri-lower alkylphosphine and the substrate is a polymeric material.
9. The method of claim 6 in which the complex is derived from silver nitrite 'and a tri-lower alkylphosphine and the substrate is a polymeric material.
10. The method of claim 6 in which the complex is derived from silver nitrite and a tri-lower alkylphosphine and the substrate is a porous ceramic body.
11. The method of claim 6 in which the complex is derived from palladium chloride and a tri-lower alkylphosphine and the substrate is a polymeric material.
12. The method of claim 4 in which the met-a1 salt/ phosphine complex and a soluble polymer are dissolved in a mutual inert volatile solvent, the solvent is evaporated to form an intimate salt/phosphine/polymer mix- 15 ture, and the mixture is heated to produce a metallized polymeric product.
13. The method of claim 12 in which the complex is derived from a salt of a heavy metal of Group I-B or VIII of the Deming Periodic Table and a trialkylphosphine.
14. The method of claim 13 in which the temperature is 100 to 350 C.
15. The method of claim 13 in which the complex is derived from gold chloride and a tri-lower alkylphosphine.
16. The method of claim 13 in which the complex is derived from silver nitrite and a tri-lower alkylphosphine.
1 6 References Cited UNITED STATES PATENTS 3,013,039 12/1961 Lambert et a1. 260-429 3,054,815 9/1962 Schroll 260439 5 3,294,828 12/1966 Werner 117-l07.2 X 3,320,293 5/1967 Colfey ll7130 X OTHER REFERENCES Mukaiyama et al., Jour. of Org. Chem, vol. 28, p. 917, 10 April 1963.
RALPH S. KENDALL, Primary Examiner.
. US. Cl. X.R.
Claims (1)
1. A METHOD OF CHEMICALLY METALIZING A SUBSTRATE WHICH COMPRISES HEATING A METAL SALT/PHOSPHINE COMPLEX DERIVED FROM ONE MOLE OF A NON-ORGANOMETALLIC SALT OF A NORMALLY SOLID HEAVY METAL OF THE DEMING PERIODIC TABLE AND 1 TO 4 MOLES OF A TRIOGANOPHOSPHINE IN WHICH EACH ORGANO GROUP IS A HYDROCARBYL OR DIHYDROCARBYLAMINO RADICAL IN THE PRESENCE OF THE SUBSTATE TO BE METALLIZED AT A TEMPERATURE OF 25* TO 350*C., BUT BELOW THE DECOMPOSITION TEMPERATURE OF THE SUBSTRATE AND THE METAL SALT ALONE, PROVIDED THAT WHEN THE SUBSTRATE IS NOT A HEAVY METAL OF THE DEMING PERIODIC TABLE OTHER THAN THE PLATING METAL, THE METAL SALT/PHOSPHINE COMPLEX IS IN SUBSTANTIALLY PURE FORM IN DIRECT CONTACT WITH THE SUBSTRATE.
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US3617340A (en) * | 1968-10-22 | 1971-11-02 | Donnelley & Sons Co | Method and composition for copperizing aluminum offset plates coated with an exposed and developed water-soluble resist |
US3625755A (en) * | 1969-04-14 | 1971-12-07 | Du Pont | Supported metal salt/phosphine complexes and metallized products therefrom |
US3655423A (en) * | 1970-03-03 | 1972-04-11 | Hooker Chemical Corp | Pretreatment of plastic surfaces before the application of an adherent organic coating |
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