CA1246767A - Solderable conductive compositions having high adhesive strength - Google Patents
Solderable conductive compositions having high adhesive strengthInfo
- Publication number
- CA1246767A CA1246767A CA000485269A CA485269A CA1246767A CA 1246767 A CA1246767 A CA 1246767A CA 000485269 A CA000485269 A CA 000485269A CA 485269 A CA485269 A CA 485269A CA 1246767 A CA1246767 A CA 1246767A
- Authority
- CA
- Canada
- Prior art keywords
- composition
- resin
- weight
- substrate
- amount
- 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
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
- B23K35/22—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
- B23K35/36—Selection of non-metallic compositions, e.g. coatings, fluxes; Selection of soldering or welding materials, conjoint with selection of non-metallic compositions, both selections being of interest
- B23K35/362—Selection of compositions of fluxes
-
- 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
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/20—Conductive material dispersed in non-conductive organic material
- H01B1/22—Conductive material dispersed in non-conductive organic material the conductive material comprising metals or alloys
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/09—Use of materials for the conductive, e.g. metallic pattern
- H05K1/092—Dispersed materials, e.g. conductive pastes or inks
- H05K1/095—Dispersed materials, e.g. conductive pastes or inks for polymer thick films, i.e. having a permanent organic polymeric binder
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/901—Printed circuit
Abstract
Patent Application of Frank St. John and Samson Shahbazi for SOLDERABLE CONDUCTIVE COMPOSTIONS HAVING
HIGH ADHESIVE STRENGTH
ABSTRACT OF THE DISCLOSURE
This invention provides conductive compositions that are directly solderable and that can be bonded directly to substrates. The compositions are made of silver exclusively in the form of flake and a resin system, said rosin system comprising phenolic rosin, acrylic resin, polyurethane resin, vinyl chloride/vinyl acetate copolymer, epoxy resin and epoxy hardener. By making a mixture of such a complex vehicle system a composition is produced that displays outstanding solderability and adhesion. Also provided is a method of making these compositions.
HIGH ADHESIVE STRENGTH
ABSTRACT OF THE DISCLOSURE
This invention provides conductive compositions that are directly solderable and that can be bonded directly to substrates. The compositions are made of silver exclusively in the form of flake and a resin system, said rosin system comprising phenolic rosin, acrylic resin, polyurethane resin, vinyl chloride/vinyl acetate copolymer, epoxy resin and epoxy hardener. By making a mixture of such a complex vehicle system a composition is produced that displays outstanding solderability and adhesion. Also provided is a method of making these compositions.
Description
~246767 BACKGROUND OF THE INVENTION
. .
1. Fleld Or the Invention ThiS invention relates to conductive compo~itions that may be used on electronic appllcations such as ele¢trical circults on printed circult boards. More partlcularly thlq invention relates to conductive composltion3 which are dl~ectly solderable and whlch can be bonded directly to substrates.
. .
1. Fleld Or the Invention ThiS invention relates to conductive compo~itions that may be used on electronic appllcations such as ele¢trical circults on printed circult boards. More partlcularly thlq invention relates to conductive composltion3 which are dl~ectly solderable and whlch can be bonded directly to substrates.
2. escrlDtlon of Prlor Art An electrlcally conductive composition ~pplled to a ~ supporting or base structure must be qufficiently ; conductlve to carry electrlc current and must be fl~mly adhered or bonded to the support or base. Furthermore, lt ; ls desirable that the conductlve composltlon be directly lS solderable.
U. S. Patent 3,030,237 dlscloses an improved coating materlal essentially comprised o~ organlc resln carrier and a sultable metalllc plgment. The lnventlon lles ln the dlscovery that a coatlng havlng a metalllc plgment component conslsting o~ a mlxture o~ ball and flake partlcles, havlng partlcular dlmenslons and used ln certain proportions, ln combination wlth an organic resin carrier, can exhibit good adhesion and electrical conductlvlty. Al~o disclo~ed 1~ that conventlonal wlre ~246767 leads may be sllver soldered to the cured coatlng u~lng entlrely common sllver solde-lng technlques.
U.S. Patent 2,959,498 dlscloses a method Or rormlng ¢onductlve sllver clrcults by rlrst applylng to a reslnous dlelectrlc sur~ace a layer Or an lncompletely cured thermosettlng re~in, and then applylng on sald layer, ln the outllne Or the deslred conductlve clrcult, a layer Or ~lnely dlvlded sllver admlxed wlth 8 thermoplastlc re~ln contalnlng a ~olvent ror both Or ~ald reslns, and then heatlng to cure both layers Or applled reslns. It 18 e~sentlal that the reslnous panel rlrst be coated wlth a thermo~ettlng resln and that thl~ resln 18 only partlally cured be~ore appllcatlon Or the conductlve composltlon.
The conduotlve clrcult 18 applled over the undercoating, 15 prererably by Jqueezlng a ~llver paste ln the deslred electrlcal clrcult pattern. The partlcles ln a thermopla~tlc realn ln a ratlo Or between 4:1 and 10:1 ~llver to resln. The resultlng ~llver clrcult pattern wlll be rlrmly adhered to the reslnous sub~trate and the ~llver llnes wlll readlly accept ~older.
U.S. Patent 4,371,459 dl~clo~es screen prlntable conductor compo~ltlon that 1~ rlexlble comprlslng (a) a conductlve phase contalnlng sllver and base metal powders dl~per~ed ln a ~olutlon Or (b) a multlpolymer prepared by copolymcrlzatlon Or vlnyl acetate, vlnyl chlorlde, and an ethylenlcally unsaturated dlcarboxyllc acld and a llnear aromatlc polyester resln dl~solved ln (c) volatlle nonhydrocarbon solvent. Tbe~e composltlons are partlcularly userul rOr appllcatlon to membrane touch awltches.
Canadian Patent Application Serial No. 463,352, F.W. Martin et al, filed September 17, 1984, discloses a solderabl~
electrlcally conductlve composltlon comprlslng metalllc sllver partlcle~ embedded ln a matrlx rormed rrom ac-yllc, carbo~ylated vlnyl and an epoxy. The composltlon 18 ormed by dlssolvlng acryllc powder and vlnyl powder ln -: ~246767 respectlve solvents to rorm a rlrst solutlon and a second solutlon. The solutlon3 are then mlxed wlth metalllc sllver partlcles and an epoxy to rorm an lnk whlch ls applled to a substrate to form a fllm thereon. The rllm ls cured to evaporate the solvent~ and allow poly~erlzatlon to occur thereby havlng a solderable electrlcally conductlve rllm.
Heretofore, conductlve composltlons developed ror use ln conne¢tlon wlth supportlng or base structures or other electrlcal equlpment have been characterlzed by unacceptably high electrlcal reslstlvlty or unacceptably low adheslon to the supportlng or base materlal.
Furthermore, many prlor art compositlons surrer rrom the deflclency Or not belng dlrectly solderable; that 18, the tlme consumlng and expenslve process Or electroless platlng or the llke must be employed ln order to apply solder to the conductlve composltlon. The composltlons that are capable Or belng soldered elther are not solderable by a varlety of solderlng technlques or do not ;~, 20 accept the solder very well. Addltlonally, many Or the prlor art composltlons cannot be bonded dlrectly to the substrate on whlch they are applled.
Whlle some prlor art composltlons do solve some Or these derlclencles they are deflclent ln that compllcated rormulatlons employlng addltlonal compounds must be used and addltlonal processlng steps must be conducted.
Furthermore, none Or the p-lor art compounds exhlblt the characterlstlcs Or surrlclent conductlvlty, and solderablllty whlle at the same tlme belng capable Or dlrect bondlng to substrates wlth outstandlng adheslon resultlng. Addltlonally, the prlor art compounds must be cured at very hlgh temperatures whlch places great energy demands on the process and adds to processlng compllcatlons.
It has been a long sought goal to provlde conductlve composltlons that have good conductlvlty, are dlrectly ~Z46767 solderable wlthout havlng to resort to the need ror compllcated procedures or formulatlons and whlch can be bonded dlrectly to substrates wlth a hlgh degree of adheslon resultlng.
SUMMARY OF THE INVENTION
It 18 thererore an obJect Or the lnventlon to provlde conductlve composltlons that are dlrectly ~olderable and whlch can be bonded dl~ectlg to substrates.
It 18 another obJect to provlde conductlve composltlons that are dl-ectly soldera~le uslng a varlety Or methods such as, for example, dlp , rerlow and wave solderlng technlques.
It 18 stlll another ob~ect to provlde composltlons wlth excellent conductivlty characterlstlcs.
It 18 a rurther obJect to provlde condu¢tlve ¢omposltlons wlth outstandlng reflow soldersblllty ~nd hlgh adheslon to the substrate on whl¢h they are applled.
; It ls ~tlll a ~urther obJect to provlde ¢omposltlons that have good aolder wettability.
It 18 another obJect to provlde compositlons that can be ¢ured at low temperatures.
It 1~ yet another obJe¢t to provlde a method ror maklng these ¢omposltlons.
Theae ob~e¢ts and others that wlll be¢ome apparent, are a¢hleved by the present lnvention, whl¢h comprlses, ln one aspe¢t, a dl-e¢tly solde-able conductlve compo~ltlon ¢omprlalng sllver ex¢luslvely ln the form Or rlake and a resln system, sald resln system comprlslng phenollc resln, a¢ryllc realn, polyurethane resln, vlnyl ¢hlo-lde/vlnyl a¢etate ¢opolymer, epoxy resln and epoxy hardener. Another aspe¢t Or the lnventlon 18 a method Or maklng a dlrectly solderable conductlve ¢omposltlon ¢omprlslng substantlally dlssolvlng phenollc reslnJ a¢ryllc resln, polyurethane resln, epoxy resln and epoxy hardener in ester solvent to rorm a flr~t solutlon, dlssolvlng vlnyl ¢hlorlde/vlnyl .' ~.
.
~246767 acetate copolymer ln ketone ~olvent to form a second solutlon and mlxlng the rlrst and second solutlons wlth silver n ake to ~orm a mlxture such that the sllver rIake 18 substantlally dlspersed and wetted. Yet another aspect of the lnventlon 19 a method Or applylng a conductlve composltlon to a substrate comprlslng bonding the conductlve composltlon dlrectly to the substrate.
CETAILED DESCRIPTION OF THE INVENTION
The composltlons Or thls lnventlon comprlse sllver excluslvely ln the rorm Or flake and a re~ln s~stem, sald re~ln sy~tem comprl~lng phenollc resln, acryllc resln, polyurethane resln, vlnyl chlorlde/vlnyl acetate copolymer, epoxy resln and cpoxy hardener. In practice the sllver rlake 1~ dlstrlbuted throughout the re~ln ~ystem.
The reJln ~y~tem not only holds the sllver flake ln suspens~on but also provlde~ adheslon Or the sflver M ake ~ to a sub~trate, holds ths sllver rlake together ~uch that ; a conductlve path 18 rormed and provldes M exlblllty.
- Furthermore, on curlng the resln pulls away rrom the sllver towards the ~ubstrate thus leavlng a hlghly enrlched ~llve- layer on top.
The compo~ltlon~ Or the lnstant lnventlon are applled ; to ~ubstrate~ while ln the llquld state, that 18, the ;~ compo~ltlon~ are ml~ed wlth a ~olvent whlch act~ as a vehlcle. Once appll d to the ~ubstrate the composltlon 18 cured and thc ~olvent evaporates leavlng a drled, cured compo~ltlon that contalns only traces Or solvent. In the rollowlng dlacusslon, ratlo~ Or certaln elements employed wlll be dlsclo~ed; lt la lmportant to polnt out that these ratlos relate to the composltlon ln lts drled and cured ~tate, not to the composltlon ln lts llquld state durlng the process Or manuracture, that 18, when contalnlng a solvent, unless otherwlse lndlcated.
It 1~ lmportant to note that ror the purpose Or thl~
lnventlon the ~llver employed must be lOOS sllver rlake.
lZ46767 Sllver ln other rorms such a8, for example, ball or mixtures or ball and rlake wlll not lead to the production r a composltlon that demon~trates all Or the advantage~
the composltlons produced accordlng to the lnstant S lnventlon. We conslder a partlcle to be ln rlake form ~; when the dlstance across the psrtlcle ls at least rlve tImes greater than the partlcle 18 thlck. Preferably, the psrtlcle ~hould be ten tlmes greater across than lt 18 thlck. The presence Or only Jllver rlake has a ~urther ;~ lO advantage ln that lt (the ~llver rlake) ~eems to contrlbute to reduclng or eliminating silver migration problems seen ln the prlor art compo~ltlons. The ~verage partlcle ~ize Or the sllver rlake may be rrom about .5 mlcrons to 50 mlcrons, préferably ln the range Or about 2 mlcrons to about 4 mlcrons. It 18 understood that sllver ~lake partlcle~ may be present havlng a partlcle ~lze Or ; les~ than .5 mlcron~ or more than 50 mlcrons; as long as the average partlcle ~lze Or the sllver ~lake 1~ between .5 mlcrons and 50 mlcron~, the composltlons o~ the lnventlon can be prepared. Ir the average partlcle ~lze Or the ~llver rlake 18 less than .5 mlcrons, there wlll be dlrrlculty ln gettlng the composltlons to load thls quantity Or ~llver. Ir the Jllver 18 too rlne, the consistency Or the compo~ltlon wlll be too clay-llke. Ir the average partlcle slze Or the ~llver rlake 18 above about 50 mlcron~, then the ¢omposltlon wlll be very lrrlcult to apply. For e~ample, the composltlon wlll tend to clog up durlng a screenlng process or the llke.
The cured composltlons Or the lnventlon contaln between about 88% and 93S, by welght, ~llver rlake.
The vlnyl chlorlde/vlnyl acetate used has a number average molecular welght range Or between about 14,000 and 35,000. Prererably, the number average molecular welght Or the copolymer 1~ about 20,000. The hlgher molecular welght vlnyl chlorlde/vlnyl acetate copolymer has better durablllty and toughness characterlstlcs than the lower 124676~7 molecular welght vlnyl chlorlde/vlnyl acetate copolymers. We have round that othe- types Or vlnyl acetate/vlnyl chlorlde copolymers do not functlon as the vlnyl chlo-lde/vlnyl acetate copolymer does Or the lnstant lnvention. E.I. DuPont de NemourQ & Co. sells a carboxyl S modlrled vlnyl chlorlde/vlnyl acetate copolymer deslgnated V.M.C.C. Thls product has a welght ratlo Or vlnyl ,~ chlorlde to vlnyl acetate to malelc acld Or 83:16:1.
Composltlons made wlth thls product deterlorate as soon as 801der 18 applled. Apparently, the presence Or the dlcarboxyll¢ acld 1~ detrlmental to the end uses dlsclosed ln thls lnventlon. A polyvlnyl butyral was also trled.
ThlJ 1~ a modlrled polyvlnyl alcohol. The composltlon made wlth thls res1n also dlslntegrated as soon as solder wa~ applled. The composltlons o~ the lnstant lnventlon lS requlre a hlgh perrormance vlnylchlorlde/vlnyl acetate copolymer; low molecular welght or modlrled vlnyl chlorlde/vlnyl acetate copolymers do not work. The welght ~ ratlo Or vlnyl chlorlde to vlnyl acetate can be rrom about ; 80:20 to about 90:10. Prererably, the welght ratlo ls rrom about 86:16 to about 88:12. The vlnyl chlorlde/vlnyl acetate copolymer havlng a nu~ber average molecular welght Or 35,000 had a welght ratlo Or vlnyl chlorlde to vlnyl acetate Or about 90:10j the vlnyl chlorlde/vlnyl acetate copolymer havlng a number average molecular welght of 14,000 had a welght ratlo Or vlnyl chlorlde to vlnyl acetate Or about 86:14.
Although the examples contained ln thls speclrlcatlon were all carrled out by a vlnyl chlorlde/vlnyl acetate copolymer deslgned VYHH supplled by Vnlon Carblde, other type~ Or vlnyl chlorlde/vlnyl acetate copolymer may be employed as long as the copolymer conforms to the specl~lcatlons herelnberore descrlbed.
~ The epoxy resln employed as part Or the resln system ; can be any type Or epoxy resin that 18 commerclally avallable and that conrorms to the the ~ollowlng S.
. . .
speclricatlons. We have used an epoxy resln ~old by Ciba Gelgy deslgnated Araldite~ 6010. Thi~ ls an unmodified llquld o~ medlum vl~coslty whlch 18 based on bl~phenol A
' a~d epichlorohydrln. The epoxy hardener employed is also ~' s supplled by Clba Gelgy and deslgnatcd HY940. The purpose o~ the epoxy ha~r ls to crossllnk wlth the epoxy resin ~, to rOrm a solld under curing condltions; the epo~y re31n and epoxy han~r employed must not crossllnk at room temperature. It muat be a one step heat curable ~ystem and be compatlble wlth the other lngredlents such as the solvent. The ~inal stlpulfltlon ls that the epo~y resin can't be a water based epoxy resin.
The phenollc resln u~ed was a one step heat curing long chaln solld phenollc'resln sold by Reichhold Chemlcal Company under the trade mark Varcum 29-112 Any slmllar type Or phenollc resln may be used as long as lt does not crossllnk at room temperature. The number average molecular welght Or the resln should be g~eater than 400 and less than 1000. or course lt must al~o be ~oluble ln ester solvent.
The acryl~c resln u~ed was a solld acryllc resln sold by Rohm and Haas Company under the trade deslgnatlon Acrylold- B-66. Any acryllc resln may be employed as long as lt ls ~oluble ln e~ter solvent.
The polyurethane resln used was obtalned from B. P. Goodrl¢h Comany. It ls ~o,ld under the trade de~lgnatlon E~tane 5702 and has a glass transltlon temperature Or rrom -10C to -50C. Other polyurethane -eslns havlng a glass transltlon temperature wlthln thls range may be used.
The ratlo used Or sllver rlake to resln system 18 lmportant. If these elements are not used wlthln the ranges Or ratlos speclrled, the compos~tlons produced will not possess all Or the characte-l~tlcs herelnberore descrlbed. In the broadest sense, the welght ratlo o~
sllver rlake to ~esln system should be rrom about 75:25 to iZ46~767.
, g about 90:10 ind prererably rrom about 80:20 to about 85:15.
Wlthin the resln system the ratlo Or epoxy re31n to epoxy han~r should be rrom about 45:55 to about 30:70.
The composltlon~ of thls lnventlon should have sllve-rlake present ln an amount Or rrom about 80% to about 85%, by welght, Or the total co0positlon, the phenollc re~ln present ln an amount Or from about .6~ to about 1.6% by welght, Or the total composltlon, the polyurethane resln present ln an amount Or r-om about .4% to about .8S, by welght, Or the total composltion, the acryllc resln present ln an amount Or rrom about .8% to about 1.6%, by welght, Or the total composltlon, the vlnyl chlorlde/vlnyl acetate copolymer present ln an amount Or from about 1.2%
to about 3.5% by welght, Or the total composltlon, the epoxy resln present ln an amount o~ rrom about l.OS to about 3.0S by welght, Or the total composltlon and the epoxy ha~ preaent ln an amount Or about 2.5S to about 4.0S, by wclght, Or the total compo~ltlon.
An advantage Or the composltlons Or the lnstant lnventlon la that they are dl-ectly solde-able. Thls means that they accept solder dlrectly wlthout the englneer havlng to resort to the use Or tlme consumlng and expenslve procedures such as electroless platlng. The composltlons can be soldered by any one Or a number Or method~ such as, ror example, dlp or reflow solderlng technlques as long as the solde- temperature does not exceed 205C. or course, the need rOr the use of a solder rlux 18 not obviated by the composltlons Or the instant lnventlon. Solder rlux 1~ a resln based mate~lal that alds the wetabllity Or composltlons. Solder flux 18 non-conductlve, 18 wldely used and 18 generally a llquld. The lux can be applled ln n varlety Or ways. Pre-rluxlng can be employed whereln the composltlon to be soldered 18 rl-st dlpped lnto llquld flux and then the solder 1~
~i applied when the composition is still wet.
Alternatively, the flux can be a component of a solder-alloy mixture. In this case, the vehicle i8 the :Elux and 5 pre-fluxing is not required. Additionally, the flux may also be activated or not activated. Activated flux cleans the surface to be soldered.
As previously indicated the composition s of the invention are applied to substrates in liquid form and 10 are then cured. The compositions of the invention can be applied to a variety of 6ubstrates that may be made from a variety of materials. Specifically, the substrates must be ceramic or resinous in nature. An example of a typical substrate is a printed circuit board. The only 15 limitation on the 6ubstrate i8 that it must be able to withstand the condition~ of the solder both without being deformed or destroyed.
The compositions of this invention are made by substantially dissolving phenolic resin, acrylic resin, 20 polyurethane resin, epoxy resin, epoxy hardener in ester solvent to form a first solution, dissolving vinyl chloride/vinyl acetate copolymer in ketone solvent to form a second solution and mixing the first and second solutions with silver flake to form a mixture such that 25 the silver flake is substantially wetted and dispersed.
The ratio of the silver flake to the first solution to the second solution is from about 65: 20: lS to about 80: 10: 10. The ratio of total resin to solvent in the first solution is from about 1: 1 to about 1: 2 and the 30 ratio of total resin to solvent in the second solution is from about 3: 1 to about 9: 1.
With respect to the total mixture the silver flake i8 preBent in an amount of from about 65% to about 80% by weight, of the total composition, the first solution is 35 present in an amount of from about 10% to about 20%, by weight, of the total composition and the second solution is present in an amount of from about 10% to about 15%, by lZ~6767 ~''.
welght, o~ the total composltlon.
There are no speclal technlques requlred ln carrylng out the method Or thls ~nventlon other than the phenollc, ; acryllc, polyuretbane and epoxy ha~ rs mu~t be substantlally dl~solved ln an ester solvent and the vlnyl chlorlde/vlnyl acetate copolymer must be d~ssolved in a ketone solvent. The sllver flake may be added by any conventlonal technlque. The ketone solvent may be any ketone solvent such as, for example, gamma butyrolactone, acetone or cyclohexane or the llke. The ester solvent can be any e~ter solvent such as, ror example, butyl Carbltol~
acetate or the llke; butyl Carbltol~ acetate ls an ester solvént supplled by Unlon Carblde.
Prlor to the appllcatlon Or the composltlon to a subatrate, the rlneness Or grlnd must be checked and round to be 25 mlcron~ or les~. Flneness o~ g-lnd can be checked ualng any standard technlque employlng a rlneness grlnd gauge. I~ the rlneness Or g-lnd 18 not 25 mlcrona or leas, then the composltlon should be paJsed throu p a 3 roll mlll untll the proper flneneas Or grlnd la obtalned. Ualng reeler gauges, the roll gaps should be ~et aa tollowa: .002~ gap between the apron roll snd mlddle roll and .015~ gap between the mlddle roll and back roll. The compoaltion ahould not be passed through the 3 roll mlll more than three tlmes. Addltlonally, the vlaco~lty Or the composltlon ahould range rrom about 30,000 c.p.a. to about 100,000 c.p.s. at 25C when mea~ured uslng a ~tandard Brookrleld vlscometer.
Prererably, the vlscoslty 18 between about 30,000 c.p.s.
~ and 70,000 c.p.s.
; 30 The mlxture 80 rormed can be applled to a substrate by any one Or a number Or technl~ues ~uch a~ by allk screenlng, spraylng, or brushing. The substrate may be lexlble or rlgld and may be Or a varlety Or types such as reslnous or ceramlc. Typlcal examples Or substrates are prlnted clrcult boards. The mlxture can be applled at a . ~
., lZ46767 thickness Or 1 mll or more. Once applled to the substrate, the mlxture 18 dried and cured at a temperatu-e Or rrom about 100C to about 170C for about 15 to about 60 mlnutes. The drylng and curlng can be carrled out by any Or a number Or technlques such as baklng ln an oven.
The composltlons Or thls invention may be bonded dlrectly to substrates. The method 18 slmply applylng a conductlve composltlon onto a substrate comprl~lng bondlng the conductlve composltlon comprlslng sllver excluslvely ln the form Or Plake and a resln system comp~lslng phenollc resln, acryllc resln, polyurethane resln, vlnyl chlorlde/vlnyl acetate copolymer, epoxy re~ln, and epoxy han~r dl-ectly to the substrate. The substrate does not need to have been precoated or pretreated wlth any compo~ltlon or by any process. Once drled and cured the compo~ltlons demonstrate excellent adheslon to the substrste. The average rorce requl-ed to remove the composltlon rrom a rlgld sub~trate 18 g-eater than 1000 p - ~
In mea~urlng the rorce requl-ed to remove (or destroy) the compo~ltlon rrom a rlgld substrate, Q pad Or composltlonal materlal 18 coated on the substrate one tenth Or an lnch square. Thls pad 18 then ~oldered. A 22 gauge tln coated copper wlre 1~ then soldered lnto the pad perpendlcular to the ~ubstrate. The force requlred to tear the pad Orr Or the substrate 18 then 0easured by conventlonal meana. Any rallure 18 ln the ablllty Or the pad to adhere to the sub~trate, not ln the wl-e adherlng to the pad. Any removal Or the composltlon or deterloratlon Or the compos~tlon 18 consldered a rallure.
In order that those skllled ln the art wlll better be able to practlce the lnventlon, the rollowlng example is glven by way Or lllustration, and not by way Or llmltatlon.
.
1246'767 EXAMPLE
Method of Making the Composition The following ingredients were m xed together and dissolved in 83.3 grams butyl Carbitol acetate to make a first solution:
16.6 grams "Varcum 29-112" (trademark) 14.3 grams "Acryloid B-66" (trademark) 9.0 grams Estane 5702 47.5 grams Araldite 6010 29.4 grams epoxy hardener - HY940 20 grams of vinyl chloride/vinyl acetate copolymer having a number average molecular weight of 20,000 was dissolved in 80 grams of gamma butyrolactone to form a second solution.
The two solutions were then mixed together with 700 grams of silver having an average particle size of 23 microns. The silver flakes were blended into the ~olution so that the flakes were wetted and dispersed.
The fineness of grind of this mixture was checked and found to be 23 microns.
The resultant mixture was applied to a printed circuit board by silk screening and then cured for 30 minutes at 165C.
U. S. Patent 3,030,237 dlscloses an improved coating materlal essentially comprised o~ organlc resln carrier and a sultable metalllc plgment. The lnventlon lles ln the dlscovery that a coatlng havlng a metalllc plgment component conslsting o~ a mlxture o~ ball and flake partlcles, havlng partlcular dlmenslons and used ln certain proportions, ln combination wlth an organic resin carrier, can exhibit good adhesion and electrical conductlvlty. Al~o disclo~ed 1~ that conventlonal wlre ~246767 leads may be sllver soldered to the cured coatlng u~lng entlrely common sllver solde-lng technlques.
U.S. Patent 2,959,498 dlscloses a method Or rormlng ¢onductlve sllver clrcults by rlrst applylng to a reslnous dlelectrlc sur~ace a layer Or an lncompletely cured thermosettlng re~in, and then applylng on sald layer, ln the outllne Or the deslred conductlve clrcult, a layer Or ~lnely dlvlded sllver admlxed wlth 8 thermoplastlc re~ln contalnlng a ~olvent ror both Or ~ald reslns, and then heatlng to cure both layers Or applled reslns. It 18 e~sentlal that the reslnous panel rlrst be coated wlth a thermo~ettlng resln and that thl~ resln 18 only partlally cured be~ore appllcatlon Or the conductlve composltlon.
The conduotlve clrcult 18 applled over the undercoating, 15 prererably by Jqueezlng a ~llver paste ln the deslred electrlcal clrcult pattern. The partlcles ln a thermopla~tlc realn ln a ratlo Or between 4:1 and 10:1 ~llver to resln. The resultlng ~llver clrcult pattern wlll be rlrmly adhered to the reslnous sub~trate and the ~llver llnes wlll readlly accept ~older.
U.S. Patent 4,371,459 dl~clo~es screen prlntable conductor compo~ltlon that 1~ rlexlble comprlslng (a) a conductlve phase contalnlng sllver and base metal powders dl~per~ed ln a ~olutlon Or (b) a multlpolymer prepared by copolymcrlzatlon Or vlnyl acetate, vlnyl chlorlde, and an ethylenlcally unsaturated dlcarboxyllc acld and a llnear aromatlc polyester resln dl~solved ln (c) volatlle nonhydrocarbon solvent. Tbe~e composltlons are partlcularly userul rOr appllcatlon to membrane touch awltches.
Canadian Patent Application Serial No. 463,352, F.W. Martin et al, filed September 17, 1984, discloses a solderabl~
electrlcally conductlve composltlon comprlslng metalllc sllver partlcle~ embedded ln a matrlx rormed rrom ac-yllc, carbo~ylated vlnyl and an epoxy. The composltlon 18 ormed by dlssolvlng acryllc powder and vlnyl powder ln -: ~246767 respectlve solvents to rorm a rlrst solutlon and a second solutlon. The solutlon3 are then mlxed wlth metalllc sllver partlcles and an epoxy to rorm an lnk whlch ls applled to a substrate to form a fllm thereon. The rllm ls cured to evaporate the solvent~ and allow poly~erlzatlon to occur thereby havlng a solderable electrlcally conductlve rllm.
Heretofore, conductlve composltlons developed ror use ln conne¢tlon wlth supportlng or base structures or other electrlcal equlpment have been characterlzed by unacceptably high electrlcal reslstlvlty or unacceptably low adheslon to the supportlng or base materlal.
Furthermore, many prlor art compositlons surrer rrom the deflclency Or not belng dlrectly solderable; that 18, the tlme consumlng and expenslve process Or electroless platlng or the llke must be employed ln order to apply solder to the conductlve composltlon. The composltlons that are capable Or belng soldered elther are not solderable by a varlety of solderlng technlques or do not ;~, 20 accept the solder very well. Addltlonally, many Or the prlor art composltlons cannot be bonded dlrectly to the substrate on whlch they are applled.
Whlle some prlor art composltlons do solve some Or these derlclencles they are deflclent ln that compllcated rormulatlons employlng addltlonal compounds must be used and addltlonal processlng steps must be conducted.
Furthermore, none Or the p-lor art compounds exhlblt the characterlstlcs Or surrlclent conductlvlty, and solderablllty whlle at the same tlme belng capable Or dlrect bondlng to substrates wlth outstandlng adheslon resultlng. Addltlonally, the prlor art compounds must be cured at very hlgh temperatures whlch places great energy demands on the process and adds to processlng compllcatlons.
It has been a long sought goal to provlde conductlve composltlons that have good conductlvlty, are dlrectly ~Z46767 solderable wlthout havlng to resort to the need ror compllcated procedures or formulatlons and whlch can be bonded dlrectly to substrates wlth a hlgh degree of adheslon resultlng.
SUMMARY OF THE INVENTION
It 18 thererore an obJect Or the lnventlon to provlde conductlve composltlons that are dlrectly ~olderable and whlch can be bonded dl~ectlg to substrates.
It 18 another obJect to provlde conductlve composltlons that are dl-ectly soldera~le uslng a varlety Or methods such as, for example, dlp , rerlow and wave solderlng technlques.
It 18 stlll another ob~ect to provlde composltlons wlth excellent conductivlty characterlstlcs.
It 18 a rurther obJect to provlde condu¢tlve ¢omposltlons wlth outstandlng reflow soldersblllty ~nd hlgh adheslon to the substrate on whl¢h they are applled.
; It ls ~tlll a ~urther obJect to provlde ¢omposltlons that have good aolder wettability.
It 18 another obJect to provlde compositlons that can be ¢ured at low temperatures.
It 1~ yet another obJe¢t to provlde a method ror maklng these ¢omposltlons.
Theae ob~e¢ts and others that wlll be¢ome apparent, are a¢hleved by the present lnvention, whl¢h comprlses, ln one aspe¢t, a dl-e¢tly solde-able conductlve compo~ltlon ¢omprlalng sllver ex¢luslvely ln the form Or rlake and a resln system, sald resln system comprlslng phenollc resln, a¢ryllc realn, polyurethane resln, vlnyl ¢hlo-lde/vlnyl a¢etate ¢opolymer, epoxy resln and epoxy hardener. Another aspe¢t Or the lnventlon 18 a method Or maklng a dlrectly solderable conductlve ¢omposltlon ¢omprlslng substantlally dlssolvlng phenollc reslnJ a¢ryllc resln, polyurethane resln, epoxy resln and epoxy hardener in ester solvent to rorm a flr~t solutlon, dlssolvlng vlnyl ¢hlorlde/vlnyl .' ~.
.
~246767 acetate copolymer ln ketone ~olvent to form a second solutlon and mlxlng the rlrst and second solutlons wlth silver n ake to ~orm a mlxture such that the sllver rIake 18 substantlally dlspersed and wetted. Yet another aspect of the lnventlon 19 a method Or applylng a conductlve composltlon to a substrate comprlslng bonding the conductlve composltlon dlrectly to the substrate.
CETAILED DESCRIPTION OF THE INVENTION
The composltlons Or thls lnventlon comprlse sllver excluslvely ln the rorm Or flake and a re~ln s~stem, sald re~ln sy~tem comprl~lng phenollc resln, acryllc resln, polyurethane resln, vlnyl chlorlde/vlnyl acetate copolymer, epoxy resln and cpoxy hardener. In practice the sllver rlake 1~ dlstrlbuted throughout the re~ln ~ystem.
The reJln ~y~tem not only holds the sllver flake ln suspens~on but also provlde~ adheslon Or the sflver M ake ~ to a sub~trate, holds ths sllver rlake together ~uch that ; a conductlve path 18 rormed and provldes M exlblllty.
- Furthermore, on curlng the resln pulls away rrom the sllver towards the ~ubstrate thus leavlng a hlghly enrlched ~llve- layer on top.
The compo~ltlon~ Or the lnstant lnventlon are applled ; to ~ubstrate~ while ln the llquld state, that 18, the ;~ compo~ltlon~ are ml~ed wlth a ~olvent whlch act~ as a vehlcle. Once appll d to the ~ubstrate the composltlon 18 cured and thc ~olvent evaporates leavlng a drled, cured compo~ltlon that contalns only traces Or solvent. In the rollowlng dlacusslon, ratlo~ Or certaln elements employed wlll be dlsclo~ed; lt la lmportant to polnt out that these ratlos relate to the composltlon ln lts drled and cured ~tate, not to the composltlon ln lts llquld state durlng the process Or manuracture, that 18, when contalnlng a solvent, unless otherwlse lndlcated.
It 1~ lmportant to note that ror the purpose Or thl~
lnventlon the ~llver employed must be lOOS sllver rlake.
lZ46767 Sllver ln other rorms such a8, for example, ball or mixtures or ball and rlake wlll not lead to the production r a composltlon that demon~trates all Or the advantage~
the composltlons produced accordlng to the lnstant S lnventlon. We conslder a partlcle to be ln rlake form ~; when the dlstance across the psrtlcle ls at least rlve tImes greater than the partlcle 18 thlck. Preferably, the psrtlcle ~hould be ten tlmes greater across than lt 18 thlck. The presence Or only Jllver rlake has a ~urther ;~ lO advantage ln that lt (the ~llver rlake) ~eems to contrlbute to reduclng or eliminating silver migration problems seen ln the prlor art compo~ltlons. The ~verage partlcle ~ize Or the sllver rlake may be rrom about .5 mlcrons to 50 mlcrons, préferably ln the range Or about 2 mlcrons to about 4 mlcrons. It 18 understood that sllver ~lake partlcle~ may be present havlng a partlcle ~lze Or ; les~ than .5 mlcron~ or more than 50 mlcrons; as long as the average partlcle ~lze Or the sllver ~lake 1~ between .5 mlcrons and 50 mlcron~, the composltlons o~ the lnventlon can be prepared. Ir the average partlcle ~lze Or the ~llver rlake 18 less than .5 mlcrons, there wlll be dlrrlculty ln gettlng the composltlons to load thls quantity Or ~llver. Ir the Jllver 18 too rlne, the consistency Or the compo~ltlon wlll be too clay-llke. Ir the average partlcle slze Or the ~llver rlake 18 above about 50 mlcron~, then the ¢omposltlon wlll be very lrrlcult to apply. For e~ample, the composltlon wlll tend to clog up durlng a screenlng process or the llke.
The cured composltlons Or the lnventlon contaln between about 88% and 93S, by welght, ~llver rlake.
The vlnyl chlorlde/vlnyl acetate used has a number average molecular welght range Or between about 14,000 and 35,000. Prererably, the number average molecular welght Or the copolymer 1~ about 20,000. The hlgher molecular welght vlnyl chlorlde/vlnyl acetate copolymer has better durablllty and toughness characterlstlcs than the lower 124676~7 molecular welght vlnyl chlorlde/vlnyl acetate copolymers. We have round that othe- types Or vlnyl acetate/vlnyl chlorlde copolymers do not functlon as the vlnyl chlo-lde/vlnyl acetate copolymer does Or the lnstant lnvention. E.I. DuPont de NemourQ & Co. sells a carboxyl S modlrled vlnyl chlorlde/vlnyl acetate copolymer deslgnated V.M.C.C. Thls product has a welght ratlo Or vlnyl ,~ chlorlde to vlnyl acetate to malelc acld Or 83:16:1.
Composltlons made wlth thls product deterlorate as soon as 801der 18 applled. Apparently, the presence Or the dlcarboxyll¢ acld 1~ detrlmental to the end uses dlsclosed ln thls lnventlon. A polyvlnyl butyral was also trled.
ThlJ 1~ a modlrled polyvlnyl alcohol. The composltlon made wlth thls res1n also dlslntegrated as soon as solder wa~ applled. The composltlons o~ the lnstant lnventlon lS requlre a hlgh perrormance vlnylchlorlde/vlnyl acetate copolymer; low molecular welght or modlrled vlnyl chlorlde/vlnyl acetate copolymers do not work. The welght ~ ratlo Or vlnyl chlorlde to vlnyl acetate can be rrom about ; 80:20 to about 90:10. Prererably, the welght ratlo ls rrom about 86:16 to about 88:12. The vlnyl chlorlde/vlnyl acetate copolymer havlng a nu~ber average molecular welght Or 35,000 had a welght ratlo Or vlnyl chlorlde to vlnyl acetate Or about 90:10j the vlnyl chlorlde/vlnyl acetate copolymer havlng a number average molecular welght of 14,000 had a welght ratlo Or vlnyl chlorlde to vlnyl acetate Or about 86:14.
Although the examples contained ln thls speclrlcatlon were all carrled out by a vlnyl chlorlde/vlnyl acetate copolymer deslgned VYHH supplled by Vnlon Carblde, other type~ Or vlnyl chlorlde/vlnyl acetate copolymer may be employed as long as the copolymer conforms to the specl~lcatlons herelnberore descrlbed.
~ The epoxy resln employed as part Or the resln system ; can be any type Or epoxy resin that 18 commerclally avallable and that conrorms to the the ~ollowlng S.
. . .
speclricatlons. We have used an epoxy resln ~old by Ciba Gelgy deslgnated Araldite~ 6010. Thi~ ls an unmodified llquld o~ medlum vl~coslty whlch 18 based on bl~phenol A
' a~d epichlorohydrln. The epoxy hardener employed is also ~' s supplled by Clba Gelgy and deslgnatcd HY940. The purpose o~ the epoxy ha~r ls to crossllnk wlth the epoxy resin ~, to rOrm a solld under curing condltions; the epo~y re31n and epoxy han~r employed must not crossllnk at room temperature. It muat be a one step heat curable ~ystem and be compatlble wlth the other lngredlents such as the solvent. The ~inal stlpulfltlon ls that the epo~y resin can't be a water based epoxy resin.
The phenollc resln u~ed was a one step heat curing long chaln solld phenollc'resln sold by Reichhold Chemlcal Company under the trade mark Varcum 29-112 Any slmllar type Or phenollc resln may be used as long as lt does not crossllnk at room temperature. The number average molecular welght Or the resln should be g~eater than 400 and less than 1000. or course lt must al~o be ~oluble ln ester solvent.
The acryl~c resln u~ed was a solld acryllc resln sold by Rohm and Haas Company under the trade deslgnatlon Acrylold- B-66. Any acryllc resln may be employed as long as lt ls ~oluble ln e~ter solvent.
The polyurethane resln used was obtalned from B. P. Goodrl¢h Comany. It ls ~o,ld under the trade de~lgnatlon E~tane 5702 and has a glass transltlon temperature Or rrom -10C to -50C. Other polyurethane -eslns havlng a glass transltlon temperature wlthln thls range may be used.
The ratlo used Or sllver rlake to resln system 18 lmportant. If these elements are not used wlthln the ranges Or ratlos speclrled, the compos~tlons produced will not possess all Or the characte-l~tlcs herelnberore descrlbed. In the broadest sense, the welght ratlo o~
sllver rlake to ~esln system should be rrom about 75:25 to iZ46~767.
, g about 90:10 ind prererably rrom about 80:20 to about 85:15.
Wlthin the resln system the ratlo Or epoxy re31n to epoxy han~r should be rrom about 45:55 to about 30:70.
The composltlon~ of thls lnventlon should have sllve-rlake present ln an amount Or rrom about 80% to about 85%, by welght, Or the total co0positlon, the phenollc re~ln present ln an amount Or from about .6~ to about 1.6% by welght, Or the total composltlon, the polyurethane resln present ln an amount Or r-om about .4% to about .8S, by welght, Or the total composltion, the acryllc resln present ln an amount Or rrom about .8% to about 1.6%, by welght, Or the total composltlon, the vlnyl chlorlde/vlnyl acetate copolymer present ln an amount Or from about 1.2%
to about 3.5% by welght, Or the total composltlon, the epoxy resln present ln an amount o~ rrom about l.OS to about 3.0S by welght, Or the total composltlon and the epoxy ha~ preaent ln an amount Or about 2.5S to about 4.0S, by wclght, Or the total compo~ltlon.
An advantage Or the composltlons Or the lnstant lnventlon la that they are dl-ectly solde-able. Thls means that they accept solder dlrectly wlthout the englneer havlng to resort to the use Or tlme consumlng and expenslve procedures such as electroless platlng. The composltlons can be soldered by any one Or a number Or method~ such as, ror example, dlp or reflow solderlng technlques as long as the solde- temperature does not exceed 205C. or course, the need rOr the use of a solder rlux 18 not obviated by the composltlons Or the instant lnventlon. Solder rlux 1~ a resln based mate~lal that alds the wetabllity Or composltlons. Solder flux 18 non-conductlve, 18 wldely used and 18 generally a llquld. The lux can be applled ln n varlety Or ways. Pre-rluxlng can be employed whereln the composltlon to be soldered 18 rl-st dlpped lnto llquld flux and then the solder 1~
~i applied when the composition is still wet.
Alternatively, the flux can be a component of a solder-alloy mixture. In this case, the vehicle i8 the :Elux and 5 pre-fluxing is not required. Additionally, the flux may also be activated or not activated. Activated flux cleans the surface to be soldered.
As previously indicated the composition s of the invention are applied to substrates in liquid form and 10 are then cured. The compositions of the invention can be applied to a variety of 6ubstrates that may be made from a variety of materials. Specifically, the substrates must be ceramic or resinous in nature. An example of a typical substrate is a printed circuit board. The only 15 limitation on the 6ubstrate i8 that it must be able to withstand the condition~ of the solder both without being deformed or destroyed.
The compositions of this invention are made by substantially dissolving phenolic resin, acrylic resin, 20 polyurethane resin, epoxy resin, epoxy hardener in ester solvent to form a first solution, dissolving vinyl chloride/vinyl acetate copolymer in ketone solvent to form a second solution and mixing the first and second solutions with silver flake to form a mixture such that 25 the silver flake is substantially wetted and dispersed.
The ratio of the silver flake to the first solution to the second solution is from about 65: 20: lS to about 80: 10: 10. The ratio of total resin to solvent in the first solution is from about 1: 1 to about 1: 2 and the 30 ratio of total resin to solvent in the second solution is from about 3: 1 to about 9: 1.
With respect to the total mixture the silver flake i8 preBent in an amount of from about 65% to about 80% by weight, of the total composition, the first solution is 35 present in an amount of from about 10% to about 20%, by weight, of the total composition and the second solution is present in an amount of from about 10% to about 15%, by lZ~6767 ~''.
welght, o~ the total composltlon.
There are no speclal technlques requlred ln carrylng out the method Or thls ~nventlon other than the phenollc, ; acryllc, polyuretbane and epoxy ha~ rs mu~t be substantlally dl~solved ln an ester solvent and the vlnyl chlorlde/vlnyl acetate copolymer must be d~ssolved in a ketone solvent. The sllver flake may be added by any conventlonal technlque. The ketone solvent may be any ketone solvent such as, for example, gamma butyrolactone, acetone or cyclohexane or the llke. The ester solvent can be any e~ter solvent such as, ror example, butyl Carbltol~
acetate or the llke; butyl Carbltol~ acetate ls an ester solvént supplled by Unlon Carblde.
Prlor to the appllcatlon Or the composltlon to a subatrate, the rlneness Or grlnd must be checked and round to be 25 mlcron~ or les~. Flneness o~ g-lnd can be checked ualng any standard technlque employlng a rlneness grlnd gauge. I~ the rlneness Or g-lnd 18 not 25 mlcrona or leas, then the composltlon should be paJsed throu p a 3 roll mlll untll the proper flneneas Or grlnd la obtalned. Ualng reeler gauges, the roll gaps should be ~et aa tollowa: .002~ gap between the apron roll snd mlddle roll and .015~ gap between the mlddle roll and back roll. The compoaltion ahould not be passed through the 3 roll mlll more than three tlmes. Addltlonally, the vlaco~lty Or the composltlon ahould range rrom about 30,000 c.p.a. to about 100,000 c.p.s. at 25C when mea~ured uslng a ~tandard Brookrleld vlscometer.
Prererably, the vlscoslty 18 between about 30,000 c.p.s.
~ and 70,000 c.p.s.
; 30 The mlxture 80 rormed can be applled to a substrate by any one Or a number Or technl~ues ~uch a~ by allk screenlng, spraylng, or brushing. The substrate may be lexlble or rlgld and may be Or a varlety Or types such as reslnous or ceramlc. Typlcal examples Or substrates are prlnted clrcult boards. The mlxture can be applled at a . ~
., lZ46767 thickness Or 1 mll or more. Once applled to the substrate, the mlxture 18 dried and cured at a temperatu-e Or rrom about 100C to about 170C for about 15 to about 60 mlnutes. The drylng and curlng can be carrled out by any Or a number Or technlques such as baklng ln an oven.
The composltlons Or thls invention may be bonded dlrectly to substrates. The method 18 slmply applylng a conductlve composltlon onto a substrate comprl~lng bondlng the conductlve composltlon comprlslng sllver excluslvely ln the form Or Plake and a resln system comp~lslng phenollc resln, acryllc resln, polyurethane resln, vlnyl chlorlde/vlnyl acetate copolymer, epoxy re~ln, and epoxy han~r dl-ectly to the substrate. The substrate does not need to have been precoated or pretreated wlth any compo~ltlon or by any process. Once drled and cured the compo~ltlons demonstrate excellent adheslon to the substrste. The average rorce requl-ed to remove the composltlon rrom a rlgld sub~trate 18 g-eater than 1000 p - ~
In mea~urlng the rorce requl-ed to remove (or destroy) the compo~ltlon rrom a rlgld substrate, Q pad Or composltlonal materlal 18 coated on the substrate one tenth Or an lnch square. Thls pad 18 then ~oldered. A 22 gauge tln coated copper wlre 1~ then soldered lnto the pad perpendlcular to the ~ubstrate. The force requlred to tear the pad Orr Or the substrate 18 then 0easured by conventlonal meana. Any rallure 18 ln the ablllty Or the pad to adhere to the sub~trate, not ln the wl-e adherlng to the pad. Any removal Or the composltlon or deterloratlon Or the compos~tlon 18 consldered a rallure.
In order that those skllled ln the art wlll better be able to practlce the lnventlon, the rollowlng example is glven by way Or lllustration, and not by way Or llmltatlon.
.
1246'767 EXAMPLE
Method of Making the Composition The following ingredients were m xed together and dissolved in 83.3 grams butyl Carbitol acetate to make a first solution:
16.6 grams "Varcum 29-112" (trademark) 14.3 grams "Acryloid B-66" (trademark) 9.0 grams Estane 5702 47.5 grams Araldite 6010 29.4 grams epoxy hardener - HY940 20 grams of vinyl chloride/vinyl acetate copolymer having a number average molecular weight of 20,000 was dissolved in 80 grams of gamma butyrolactone to form a second solution.
The two solutions were then mixed together with 700 grams of silver having an average particle size of 23 microns. The silver flakes were blended into the ~olution so that the flakes were wetted and dispersed.
The fineness of grind of this mixture was checked and found to be 23 microns.
The resultant mixture was applied to a printed circuit board by silk screening and then cured for 30 minutes at 165C.
Claims (22)
1. A directly solderable conductive composition comprising silver exclusively in the form of flake and a resin system, said resin system comprising phenolic resin, acrylic resin, polyurethane resin, vinyl chloride/vinyl acetate copolymer, epoxy resin and epoxy hardener, the weight ratio of silver flake to resin system being from about 75:25 to about 90:10.
2. The composition of claim 1 wherein the weight ratio of silver flake to resin system is from about 80:20 to about 85:15.
3. The composition of claim 1 wherein the ratio of epoxy resin to epoxy hardener is from about 45:55 to about 30:70.
4. The composition of claim 1 wherein silver flake is prevent in an amount of from about 80% to 85%, by weight, of the total composition, the phenolic resin is present in an amount of from about .6% to about 1.6%, by weight, of the total composition, the acrylic resin is present in an amount of from about .8% to about 1.6%, by weight, of the total composition, the polyurethane resin is present in an amount of from about .4% to .8%, by weight, of the total composition, the vinyl chloride/vinyl acetate copolymer is prevent in an amount of from about 1.2% to about 3.5%, by weight, of the total composition, the epoxy resin is present in an amount of from about 1.0%
to about 3.0%, by weight, of the total composition and the epoxy hardener is present in an amount of from about 2.5%
to about 4.0%, by weight, of the total composition,
to about 3.0%, by weight, of the total composition and the epoxy hardener is present in an amount of from about 2.5%
to about 4.0%, by weight, of the total composition,
5. The composition of claim 1 wherein the particle size of the silver flake is from about .5 microns to about 50 microns.
6. The composition of claim 1 wherein the ratio of vinyl chloride to vinyl acetate is from about 80:20 to about 90:10.
7. An article comprising a substrate coated with the composition of claim 1.
8. The article of claim 7 wherein the substrate is a printed circuit board.
9. The article Or claim 7 wherein the force required to remove the conductive composition from the substrate is from about 1000 p.s.i. to about 1800 p.s.i.
10. A method of soldering the composition of claim 1 comprising applying solder directly to the composition.
11. The method of claim 10 wherein the solder is applied at a temperature of 205°C or less.
12. The method of claim 10 wherein the solder is applied by dip or reflow soldering techniques.
13. A method of making a directly solderable conductive composition comprising substantially dissolving phenolic resin, acrylic resin, polyurethane resin, epoxy resin and epoxy hardener in an ester solvent to form a first solution, dissolving vinyl chloride/vinyl acetate copolymer in ketone solvent to form a second solution and mixing the first and second solutions with silver flake to form a mixture wherein the weight ratio of silver flake to resin is from about 75:25 to about 90:10.
14. The method of claim 13 wherein the ratio of silver flake to the first solution to the second solution is from about 65:20:15 to about 80:10:10.
15. The method of claim 13 wherein the ratio of total resin to solvent in the first solution is from about 1:1 to about 1:2 and the ratio of total resin to solvent in the second solution is from about 3:1 to about 9:1.
16. The method of claim 13 wherein the silver flake is present in an amount of from about 65% to about 80%, by weight, of the total composition, the first solution is present in an amount of from about 10% to about 20%, by weight, of the total composition and the second solution is present in an amount of from about 10% to about 15%, by weight, of the total composition.
17. The method of claim 13 additionally comprising applying the mixture to a substrate, then drying and curing the mixture.
18. The method of claim 17 wherein the substrate is a printed circuit board.
19. The method of claim 17 wherein the mixture is dried and cured at a temperature of from about 125°C to about 180°C for about 15 minutes to about 120 minutes.
20. A method of applying a conductive composition to a substrate comprising bonding the conductive composition of claim 1 directly to the substrate.
21. The method of claim 20 wherein the force required to remove the conductive composition from the substrate is greater than 1000 p.s.i.
22. The method of claim 20 wherein the substrate is a printed circuit board.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US631,974 | 1984-07-18 | ||
| US06/631,974 US4595606A (en) | 1984-07-18 | 1984-07-18 | Solderable conductive compositions having high adhesive strength |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1246767A true CA1246767A (en) | 1988-12-13 |
Family
ID=24533555
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000485269A Expired CA1246767A (en) | 1984-07-18 | 1985-06-26 | Solderable conductive compositions having high adhesive strength |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4595606A (en) |
| EP (1) | EP0169060B1 (en) |
| JP (1) | JPS6140316A (en) |
| KR (1) | KR860000921A (en) |
| AT (1) | ATE36919T1 (en) |
| CA (1) | CA1246767A (en) |
| DE (1) | DE3564743D1 (en) |
| PH (1) | PH21722A (en) |
| SG (1) | SG86788G (en) |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4680141A (en) * | 1984-11-29 | 1987-07-14 | Mcdonnell Douglas Corporation | Solder composition |
| US4673532A (en) * | 1986-01-22 | 1987-06-16 | Mcdonnell Douglas Corporation | Rosin-free solder composition |
| AU8107987A (en) * | 1986-09-30 | 1988-04-21 | Wilde Membran Impulstechnik G.m.b.H. | Electrically conductive structure with applied metallization |
| DE3724013A1 (en) * | 1987-07-21 | 1989-02-02 | Flachglas Ag | METHOD OF APPLYING A COLORED COATING ON A SURFACE OF A GLASS PAN |
| US5147453A (en) * | 1987-11-03 | 1992-09-15 | Basf Corporation | Paint compositions containing silver metal flake pigment |
| US4896250A (en) * | 1988-02-12 | 1990-01-23 | Emerson & Cuming, Inc. | Solvent-processible electrically conductive coatings |
| US5006575A (en) * | 1989-10-20 | 1991-04-09 | E. I. Du Pont De Nemours And Company | Die attach adhesive composition |
| US5180523A (en) * | 1989-11-14 | 1993-01-19 | Poly-Flex Circuits, Inc. | Electrically conductive cement containing agglomerate, flake and powder metal fillers |
| US5183593A (en) * | 1989-11-14 | 1993-02-02 | Poly-Flex Circuits, Inc. | Electrically conductive cement |
| US5089173A (en) * | 1990-05-02 | 1992-02-18 | Advanced Products Inc. | Highly conductive polymer thick film compositions |
| JPH0412595A (en) * | 1990-05-02 | 1992-01-17 | Mitsubishi Petrochem Co Ltd | Conductive paste composition |
| US5141777A (en) * | 1990-05-02 | 1992-08-25 | Advanced Products, Inc. | Highly conductive polymer thick film compositions |
| US5112687A (en) * | 1990-05-02 | 1992-05-12 | Advanced Products Inc. | Highly conductive polymer thick film compositions |
| US5136365A (en) * | 1990-09-27 | 1992-08-04 | Motorola, Inc. | Anisotropic conductive adhesive and encapsulant material |
| JPH07123179B2 (en) * | 1990-10-05 | 1995-12-25 | 信越ポリマー株式会社 | Circuit board connection structure with anisotropic conductive adhesive |
| US5283007A (en) * | 1992-04-28 | 1994-02-01 | E. I. Du Pont De Nemours And Company | Conductive polymer compositions |
| WO1992020073A2 (en) * | 1991-05-01 | 1992-11-12 | E.I. Du Pont De Nemours And Company | Conductive polymer compositions |
| JPH04345664A (en) * | 1991-05-01 | 1992-12-01 | Du Pont Japan Ltd | Conductive resin composition |
| JPH0521208A (en) * | 1991-05-07 | 1993-01-29 | Daito Tsushinki Kk | Ptc element |
| JPH0826251B2 (en) * | 1991-06-05 | 1996-03-13 | 福田金属箔粉工業株式会社 | Silver powder for baking type conductive paint and baking type conductive paint using the same |
| JP2730357B2 (en) * | 1991-11-18 | 1998-03-25 | 松下電器産業株式会社 | Electronic component mounted connector and method of manufacturing the same |
| US5447267A (en) * | 1993-02-08 | 1995-09-05 | Matsushita Electric Industrial Co., Ltd. | Method of soldering electronic part using a bond for tacking the electronic part |
| US5780143A (en) * | 1995-03-01 | 1998-07-14 | Tokuyama Corporation | Circuit board |
| JPH09116273A (en) * | 1995-08-11 | 1997-05-02 | Shinko Electric Ind Co Ltd | Multilayered circuit board and its manufacture |
| JPH0959553A (en) * | 1995-08-30 | 1997-03-04 | Dainippon Printing Co Ltd | Transparent electroconductive ink |
| KR100269830B1 (en) * | 1996-04-18 | 2000-10-16 | 포만 제프리 엘 | Organic-metallic composite coating for copper surface protection |
| KR100629923B1 (en) * | 1998-09-30 | 2006-09-29 | 돗빤호무즈가부시기가이샤 | Conductive paste, curing method therof, method for fabricating antenna for contactless data transmitter-receiver, and contactless data transmitter-receiver |
| US6750301B1 (en) * | 2000-07-07 | 2004-06-15 | National Starch And Chemical Investment Holding Corporation | Die attach adhesives with epoxy compound or resin having allyl or vinyl groups |
| JP2005234464A (en) * | 2004-02-23 | 2005-09-02 | Tdk Corp | Optical transceiver and optical module used therefor |
| EP2481060B1 (en) * | 2009-09-24 | 2015-07-15 | E. I. du Pont de Nemours and Company | Polymer thick film silver electrode composition for use as a plating link |
| US20120119163A1 (en) * | 2010-11-17 | 2012-05-17 | E. I. Du Pont De Nemours And Company | Solderable polymer thick film silver electrode composition for use in thin-film photovoltaic cells and other applications |
| US8704087B2 (en) | 2011-06-01 | 2014-04-22 | E I Du Pont De Nemours And Company | Solderable polymer thick film conductive electrode composition for use in thin-film photovoltaic cells and other applications |
| JP6233792B2 (en) * | 2013-01-28 | 2017-11-22 | 国立大学法人群馬大学 | Conductive paste |
| EP2918371A1 (en) * | 2014-03-11 | 2015-09-16 | Heraeus Precious Metals North America Conshohocken LLC | Solderable conductive polymer thick film composition |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3412043A (en) * | 1966-08-05 | 1968-11-19 | Dexter Corp | Electrically conductive resinous compositions |
| GB1251834A (en) * | 1968-04-02 | 1971-11-03 | ||
| JPS57185316A (en) * | 1981-05-11 | 1982-11-15 | Sumitomo Metal Mining Co Ltd | Electrically conductive resin paste |
| US4371459A (en) * | 1981-12-17 | 1983-02-01 | E. I. Du Pont De Nemours And Company | Flexible screen-printable conductor composition |
| US4535012A (en) * | 1983-09-30 | 1985-08-13 | Electro Materials Corp. Of America | Fast curing solderable conductor |
| US4564563A (en) * | 1983-09-30 | 1986-01-14 | Electro Materials Corp. Of America | Solderable conductor |
-
1984
- 1984-07-18 US US06/631,974 patent/US4595606A/en not_active Expired - Fee Related
-
1985
- 1985-06-26 CA CA000485269A patent/CA1246767A/en not_active Expired
- 1985-07-02 PH PH32475A patent/PH21722A/en unknown
- 1985-07-16 KR KR1019850005082A patent/KR860000921A/en not_active Application Discontinuation
- 1985-07-17 DE DE8585305082T patent/DE3564743D1/en not_active Expired
- 1985-07-17 AT AT85305082T patent/ATE36919T1/en not_active IP Right Cessation
- 1985-07-17 EP EP85305082A patent/EP0169060B1/en not_active Expired
- 1985-07-17 JP JP15796285A patent/JPS6140316A/en active Pending
-
1988
- 1988-12-08 SG SG867/88A patent/SG86788G/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0169060B1 (en) | 1988-08-31 |
| DE3564743D1 (en) | 1988-10-06 |
| PH21722A (en) | 1988-02-03 |
| EP0169060A2 (en) | 1986-01-22 |
| KR860000921A (en) | 1986-02-20 |
| JPS6140316A (en) | 1986-02-26 |
| EP0169060A3 (en) | 1986-08-27 |
| ATE36919T1 (en) | 1988-09-15 |
| US4595606A (en) | 1986-06-17 |
| SG86788G (en) | 1989-06-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA1246767A (en) | Solderable conductive compositions having high adhesive strength | |
| CA1254323A (en) | Conductive compositions that are directly solderable and flexible and that can be bonded directly to substrates | |
| US4447492A (en) | Articles having an electrically conductive surface | |
| US4548879A (en) | Solderable polymer thick films | |
| KR100832628B1 (en) | Conductive paste | |
| CA2727611A1 (en) | Conductive inks and pastes | |
| EP0667031A1 (en) | Electrically conductive resin pastes and multilayer ceramic capacitors having a terminal electrode comprised of the same | |
| JPH0421721B2 (en) | ||
| US4517118A (en) | New nickel coating composition for shielding electronic equipment and the like | |
| JP4928021B2 (en) | Conductive adhesive and circuit using the same | |
| EP1229088A1 (en) | Electrically conductive ink or paint, process for the preparation thereof and writing implements having the ink packed therein | |
| CA1262589A (en) | Low resistance resistor compositions | |
| JPS62230869A (en) | Electrically conductive coating compound to be soldered | |
| JPS6350384B2 (en) | ||
| JPH1166956A (en) | Conductive paste | |
| US4786437A (en) | One-component, particle-filled compositions | |
| JPH0149390B2 (en) | ||
| JP2005082632A (en) | Anisotropically conducting adhesive and connection structure | |
| JPH0249352B2 (en) | ||
| KR20220147611A (en) | Conductive paste and conductive pattern using same | |
| CN1010524B (en) | Weldable conductive composite with high adhesive strength | |
| JPH024627B2 (en) | ||
| CN1009734B (en) | Weldable thick polymeric coatings | |
| JPH0585588B2 (en) | ||
| JPH047369A (en) | Electron beam curing conductive paste composition |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |