Selective catalytic activation of non-conductive substrates

Abstract

A process of providing a pattern of a metal on a non-conductive substrate to create loop antennae for wireless articles and for creating circuitry for smart cards, such as phone cards is provided. The method comprises the steps of catalyzing the non-conductive substrate by applying a catalytic ink, reducing a source of catalytic metal ions in the catalytic ink to its associated metal, depositing electroless metal on the pattern of catalytic ink on the surface of the substrate; and plating electrolytic metal on the electroless metal layer to produce the desired pattern of metal on the non-conductive substrate. The catalytic ink typically comprises one or more solvents, a source of catalytic metal ions, a crosslinking agent, one or more copolymers, a polyurethane polymer, and, optionally, one or more fillers.

1 . A method of providing a pattern of a metal on a non-conductive substrate, the method comprising the steps of: 
 a) applying a catalytic ink in a desired pattern on a surface of the non-conductive substrate, wherein the catalytic ink comprises:    a source of catalytic metal ions;    b) reducing the source of catalytic metal ions to its associated metal with a suitable reducing agent;    c) plating metal on the pattern of catalytic ink.    
     
     
         2 . The method according to  claim 1 , wherein the catalytic ink is applied by printing it onto the substrate.  
     
     
         3 . The method according to  claim 1 , wherein the catalytic ink comprises a solvent selected from the group consisting of aromatic and aliphatic hydrocarbons, glycerol, ketones, esters, glycol ethers, and esters of glycol ethers.  
     
     
         4 . The method according to  claim 3 , wherein the solvent is selected from the group consisting of toluene, xylene, glycerol, methyl ethyl ketone, cyclohexanone, butyl acetate, dioctyl phthalate, butyl glycolate, ethylene glycol monomethyl ether, diethylene glycol dimethyl ether, propylene glycol monomethyl ether, ethylene glycol acetate, propylene glycol monomethyl ether-acetate, acetone, isophorone, methyl propyl ketone, methyl amyl ketone, diacetone-alcohol, and combinations of the foregoing.  
     
     
         5 . The method according to  claim 4 , wherein the solvent is cyclohexanone.  
     
     
         6 . The method according to  claim 1 , wherein the catalytic metal ions are selected from the group consisting of palladium, gold, silver, platinum, copper, and combinations of the foregoing.  
     
     
         7 . The method according to  claim 6 , wherein the catalytic metal ions comprise palladium.  
     
     
         8 . The method according to  claim 7 , wherein the source of palladium is selected from the group consisting of palladium dichloride and palladium acetate.  
     
     
         9 . The method according to  claim 8 , wherein the source of palladium is a solution of about 10% to about 20% palladium dichloride in water with hydrochloric acid.  
     
     
         10 . The method according to  claim 8 , wherein the source of palladium is a solution of about 0.1% to about 2% palladium acetate in cyclohexanone.  
     
     
         11 . The method according to  claim 1 , wherein the catalytic ink comprises a crosslinking agent is comprising a polyisocyanate.  
     
     
         12 . The method according to  claim 1 , wherein the catalytic ink comprises a copolymer comprising vinyl chloride and hydroxylpropyl acrylate.  
     
     
         13 . The method according to  claim 1 , wherein the catalytic ink comprises one or more fillers selected from the group consisting of talc, oxides of manganese, titanium, magnesium, aluminum, bismuth, copper, nickel, tin, zinc, and silicon, silicates, bentonites, chalk, carbon black, and combinations of the foregoing.  
     
     
         14 . The method according to  claim 13 , wherein the one or more fillers comprise talc and fumed silica.  
     
     
         15 . The method according to  claim 1 , wherein the non-conductive substrate is selected from the group consisting of polyimides, polyethylene terephthalate, polyesters, acrylonitrile-butadiene-styrene, polyvinylidine chloride, paper and polycarbonates.  
     
     
         16 . The method according to  claim 15 , wherein the non-conductive substrate is polyethylene terephthalate.  
     
     
         17 . The method according to  claim 1 , wherein the source of catalytic metal ions is reduced to its associated metal with a reducing agent selected from the group consisting of sodium borohydride, hydrazine, hydrazine hydrate, hydrazine sulfate, and dihydrazine sulfate.  
     
     
         18 . The method according to  claim 17 , wherein the reducing agent is sodium borohydride.  
     
     
         19 . The method according to  claim 1 , wherein the plating is selected from the group consisting of electroless copper, electroless nickel, and combinations thereof.  
     
     
         20 . The method according to  claim 1 , wherein the plating is plated using an acid copper plating bath.  
     
     
         21 . (canceled)  
     
     
         22 . A method of providing a pattern of a metal on a non-conductive substrate, the method comprising the steps of: 
 a) applying a catalytic ink on a surface of the non-conductive substrate, wherein the catalytic ink comprises:    a source of catalytic metal ions;    b) reducing the source of catalytic metal ions to be its associated metal with a suitable reducing agent;    c) plating metal on the catalytic ink on the surface of the substrate;    d) printing a UV etch resist with the desired pattern; and    e) etching away the plated metal between the resist to define the desired circuit.    
     
     
         23 . The method according to  claim 22 , wherein the catalytic ink is applied by printing.  
     
     
         24 . The method according to  claim 22 , wherein the catalytic ink comprises a solvent is selected from the group consisting of aromatic and aliphatic hydrocarbons, glycerol, ketones, esters, glycol ethers, and esters of glycol ethers.  
     
     
         25 . The method according to  claim 24 , wherein the solvent is selected from the group consisting of toluene, xylene, glycerol, methyl ethyl ketone, cyclohexanone, butyl acetate, dioctyl phthalate, butyl glycolate, ethylene glycol monomethyl ether, diethylene glycol dimethyl ether, propylene glycol monomethyl ether, ethylene glycol acetate, propylene glycol monomethyl ether-acetate, acetone, isophorone, methyl propyl ketone, methyl amyl ketone, diacetone-alcohol and combinations of the foregoing.  
     
     
         26 . The method according to  claim 25 , wherein the solvent is cyclohexanone.  
     
     
         27 . The method according to  claim 22 , wherein the catalytic metal ions are selected from the group consisting of palladium, gold, silver, platinum, copper, and combinations of the foregoing.  
     
     
         28 . The method according to  claim 27 , wherein the catalytic metal ions comprise palladium.  
     
     
         29 . The method according to  claim 28 , wherein the source of palladium is selected from the group consisting of palladium dichloride and palladium acetate.  
     
     
         30 . The method according to  claim 29 , wherein the source of palladium is a solution of about 10% to about 20% palladium dichloride in water with hydrochloric acid.  
     
     
         31 . The method according to  claim 29 , wherein the source of palladium is a solution of about 0.1 % to about 2% palladium acetate in cyclohexanone.  
     
     
         32 . (canceled)  
     
     
         33 . The method according to  claim 22 , wherein the catalytic ink comprises a copolymer comprising vinyl chloride and hydroxylpropyl acrylate.  
     
     
         34 . The method according to  claim 22 , wherein the catalytic ink comprises one or more fillers selected from the group consisting of talc, oxides of manganese, titanium, magnesium, aluminum, bismuth, copper, nickel, tin, zinc, and silicon, silicates, bentonites, chalk, carbon black, and combinations of the foregoing.  
     
     
         35 . The method according to  claim 34 , wherein the one or more fillers comprise talc and fumed silica.  
     
     
         36 . The method according to  claim 22 , wherein the non-conductive substrate is selected from the group consisting of polyimides, polyethylene terephthalate, polyesters, acrylonitrile-butadiene-styrene, polyvinylidine chloride, and polycarbonates.  
     
     
         37 . The method according to  claim 36 , wherein the non-conductive substrate is polyethylene terephthalate.  
     
     
         38 . The method according to  claim 22 , wherein the source of catalytic metal ions is reduced to its associated metal with a reducing agent selected from the group consisting of sodium borohydride, hydrazine, hydrazine hydrate, hydrazine sulfate, and dihydrazine sulfate.  
     
     
         39 . The method according to  claim 38 , wherein the reducing agent is sodium borohydride.  
     
     
         40 . The method according to  claim 22 , wherein the plating is selected from the group consisting of electroless copper, electroless nickel, and combinations thereof.  
     
     
         41 . The method according to  claim 22 , wherein the plating is plated using an acid copper plating bath.  
     
     
         42 . (canceled)  
     
     
         43 . A method of providing a desired pattern of metal on a non-conductive substrate comprising the steps of: 
 a) applying a catalytic ink on a surface of the non-conductive substrate, wherein the catalytic ink comprises    a source of catalytic metal ions:    b) reducing the source of catalytic metal ions to its associated metal using a suitable reducing agent;    c) printing resist in a desired pattern on the catalytic ink;    d) plating metal on the catalytic ink in the areas not covered by the printed resist.    
     
     
         44 . The method according to  claim 43 , wherein the catalytic ink is applied by printing.  
     
     
         45 . The method according to  claim 43 , wherein the catalytic ink comprises solvent selected from the group consisting of aromatic and aliphatic hydrocarbons, glycerol, ketones, esters, glycol ethers, and esters of glycol ethers.  
     
     
         46 . The method according to  claim 45 , wherein the solvent is selected from the group consisting of toluene, xylene, glycerol, methyl ethyl ketone, cyclohexanone, butyl acetate, dioctyl phthalate, butyl glycolate, ethylene glycol monomethyl ether, diethylene glycol dimethyl ether, propylene glycol monomethyl ether, ethylene glycol acetate, propylene glycol monomethyl ether-acetate, acetone, isophorone, methyl propyl ketone, methyl amyl ketone, diacetone-alcohol and combinations of the foregoing.  
     
     
         47 . The method according to  claim 46 , wherein the solvent is cyclohexanone.  
     
     
         48 . The method according to  claim 43 , wherein the catalytic metal ions are selected from the group consisting of palladium, gold, silver, platinum, copper, and combinations of the foregoing.  
     
     
         49 . The method according to  claim 48 , wherein the catalytic metal ions comprise palladium.  
     
     
         50 . The method according to  claim 49 , wherein the source of palladium is selected from the group consisting of palladium dichloride and palladium acetate.  
     
     
         51 . The method according to  claim 50 , wherein the source of palladium is a solution of about 10% to about 20% palladium dichloride in water with hydrochloric acid.  
     
     
         52 . The method according to  claim 50 , wherein the source of palladium is a solution of about 0.1 % to about 2% palladium acetate in cyclohexanone.  
     
     
         53 . The method according to  claim 43 , wherein the catalytic ink comprises a crosslinking agent comprising a polyisocyanate.  
     
     
         54 . The method according to  claim 43 , wherein the catalytic ink comprises a copolymer comprising vinyl chloride and hydroxylpropyl acrylate.  
     
     
         55 . The method according to  claim 43 , wherein the catalytic ink comprises one or, more fillers selected from the group consisting of talc, oxides of manganese, titanium, magnesium, aluminum, bismuth, copper, nickel, tin, zinc, and silicon, silicates, bentonites, chalk, carbon black, and combinations of the foregoing.  
     
     
         56 . The method according to  claim 55 , wherein the one or more fillers comprise talc and fumed silica.  
     
     
         57 . The method according to  claim 43 , wherein the non-conductive substrate is selected from the group consisting of polyimides, polyethylene terephthalate, polyesters, acrylonitrile-butadiene-styrene, polyvinylidine chloride, and polycarbonates.  
     
     
         58 . The method according to  claim 57 , wherein the non-conductive substrate is polyethylene terephthalate.  
     
     
         59 . The method according to  claim 43 , wherein the source of catalytic metal ions is reduced to its associated metal with a reducing agent selected from the group consisting of sodium borohydride, hydrazine, hydrazine hydrate, hydrazine sulfate, and dihydrazine sulfate.  
     
     
         60 . The method according to  claim 59 , wherein the reducing agent is sodium borohydride.  
     
     
         61 . The method according to  claim 43 , wherein the plating is selected from the group consisting of electroless copper, electroless nickel, and combinations thereof.  
     
     
         62 . The method according to  claim 43 , wherein the electrolytic metal plating is plated using an acid copper plating bath.  
     
     
         63 . (canceled)