Background

Adhesives find wide applications in optical displays. Such applications include, but are not limited to, bonding polarizers to modules of a liquid crystal display (LCD) and attaching various optical films to a glass lens in mobile hand held devices (MHH). The polarizers may be in direct or indirect contact with the adhesive.

Recently, there has been an upward trend to introduce and combine touch panel functions in various display applications. Touch panels typically include a corrosion sensitive layer, such as a layer of indium-tin oxide, coated polyethylene terephtalate film or coated on glass. These coated substrates are often attached to the display modules using adhesives. In some touch panel designs, the adhesive contacts the corrosion sensitive layer. In other display applications, the adhesive may also contact corrosion sensitive layers such as vapor coated mirror surfaces or electro-magnetic interference shielding layers. These layers are also frequently derived from metals and metal alloys that are electro-conductive.

Summary

The present disclosure addresses the need for an adhesive that is compatible with a corrosion sensitive layer, such as a metal or metal alloy. That is, the adhesive only minimally changes the resistance of such layer once in contact with it. In this disclosure, the following definitions are used:

"a change" as used to describe the electrical resistance that the corrosion sensitive layer exhibits means generally an absolute value difference in electrical resistance of the layer as before and after conditioning;

"acid number" generally denotes the acid content of the polymer and is defined as the amount of potassium hydroxide (typically in milligrams) that is needed to neutralize the acids in one gram of polymer, generally following ASTM D974;

"addition cure silicone" generally involves a reaction of a vinyl terminated oligomer/polymer, such as a vinyl terminated polydimethylsiloxane (PDMS), with a hydride containing oligomer/polymer, such as a PDMS containing a silicon hydride, typically in the presence of a platinum catalyst; "adhesive" generally means a viscoelastic material having viscous and elastic components such that while the adhesive displays some level of resiliency under compressive stress, it is generally not a spring-like material, i.e., it is not an elastic solid;

"corrosion sensitive layer" means generally a layer that is susceptible to oxidation upon exposure to air and moisture, and the layer is capable of carrying a current once a voltage is applied to it;

"cure-in-place adhesive" generally means a liquid system that can be delivered to a desired location where the adhesive components either nearly spontaneously react with each other or do so when exposed to an energy source (such as heat or radiation);

"heat activated adhesive" generally means an adhesive that exhibits substantially no tack in dry form using finger pressure at room temperature but with exposure to elevated temperatures, the adhesive is tacky, wets out the substrate surfaces well, and after cooling to room temperature, adheres to a variety of dissimilar surfaces;

"microstructure" as used to describe any generic layer or substrate generally means one that contains repeating structures projecting from a major surface of the layer, the structures can be in a variety of form, including but not limited to, peaks and pyramids;

"optically clear" generally means that a material exhibits about 5% or less haze, as measured on a 25 micrometer thick sample in the manner described below in the Example section; and

"pressure sensitive adhesive" generally means that the adhesive is aggressively and permanently tacky in dry form at room temperature and firmly adheres to a variety of dissimilar surfaces.

In one aspect, the present disclosure pertains to an article comprising an adhesive having an acid number of less than about 5 and selected from the group consisting of polyurea, polyamide, polyurethane, polyester, addition cure silicone and combinations thereof in contact with a corrosion sensitive layer selected from the group of metal and metal alloys, wherein when the article is conditioned for about 21 days at about 6O ⁰ C and 90% relative humidity, the corrosion sensitive layer exhibits a change from its initial electrical resistance value of 20% or less. In one embodiment, the adhesive and corrosion sensitive layer are disposed on a first major surface of a substrate such that the corrosion sensitive layer and optionally the adhesive are in contact with the first major surface of the substrate. In another aspect, the present disclosure pertains to a method of making an article comprising the steps of: (i) providing a substrate having a corrosion sensitive layer disposed on at least a portion thereof; (ii) providing a tape comprising (a) a backing having opposing first and second major surfaces, (b) an adhesive having an acid number of less than about 5 and selected from the group consisting of polyurea, polyamide, polyurethane, polyester, addition cure silicone and combinations thereof; and (iii) laminating the tape to the substrate such that the adhesive contacts the corrosion sensitive layer. The corrosion sensitive layers disclosed herein are substantially flat; i.e., they do not contain microstructures. In other embodiments, the backing, if a tape is used, or the substrate is substantially flat.

In one exemplary application, the articles and the method of making the articles described in the present disclosure can be integrated into electronic devices such as, but not limited to, liquid crystal display panel, capacitive type touch panels, cell phones, hand held devices, and a laptop computers.

Other features and advantages will be apparent from the following detailed description and the claims. The above summary is not intended to describe each illustrated embodiment or every implementation of the present disclosure. The detailed description that follows more particularly exemplifies certain presently preferred embodiments using the principles disclosed herein.

Brief Description of the Drawings

The invention can be better described with reference to the drawings, wherein:

Figure 1 is a top plan view of an exemplary article according to the present disclosure;

Figure 2 is a cross-sectional view of another exemplary article according to the present disclosure;

Figure 3 is a schematic view of an exemplary method of making an article according to the present disclosure;

Figures 4A and 4B are schematic views of another exemplary method of making an article according to the present disclosure;

Figure 5 is a cross-sectional view of another exemplary article according to the present disclosure; and Figure 6 shows the relationship of the resistance change as a function of time for Examples 1 to 5 and a Control sample during various stages of conditioning.

The figures are idealized, are not drawn to scale, and are intended only for illustrative purposes.

Detailed Description

All numbers are herein assumed to be modified by the term "about." The recitation of numerical ranges by endpoints includes all numbers subsumed within that range (e.g., 1 to 5 includes 1, 1.5, 2, 2.75, 3, 3.80, 4, and 5). All parts recited herein are by weight unless otherwise indicated.

Turning now to the figures, Figure 1 shows a top plan view of an article 1 that can be used in electronic devices. The article includes a substrate 4 having a plurality of corrosion sensitive traces 5, in the form of a grid, disposed on a first major surface of the substrate. A connector pad 6 lies adjacent to each end of the corrosion sensitive trace. When a current is applied to the connector pads, they are in electrical communication with the corrosion sensitive traces. The adhesive disclosed herein will typically be applied to the substrate such that it is in direct contact with the corrosion sensitive layer and the first major surface of the substrate.

Figure 2 depicts a cross-sectional view of an exemplary article 10 having a plurality of alternating layers of adhesive 18 and substrate 14 having a corrosion sensitive layer 15 disposed on a first surface 14a of the substrate. Connector pads 16 lie adjacent to the edge of the substrate. The connector pads are in communication with the corrosion sensitive layer such that the pads and the corrosion sensitive layers are in electrical communication with one another when current passes through the layer 15. While only two sets of alternating layers of the substrate and adhesive are shown, it is within the scope of the present disclosure to use a higher number of alternating layers or to use one set of substrate and adhesive.

Figure 3 depicts a schematic view of an exemplary process of making an article. The process includes a step of providing a first substrate 24 having a non-continuous corrosion sensitive layer 25 disposed on first surface 24a of the substrate. Connector pads 26 lie adjacent to the substrate, as in Figure 1. A roll of tape 20 has an adhesive 28 coated on a backing 21. Optionally, the backing includes release coatings allowing for the roll of tape to unwind. The tape is laminated to the first surface 24a of the first substrate 24 such that the adhesive 28 is in contact with the corrosion sensitive layer and the exposed portion of the first surface 24a i.e., that portion that is not covered by the corrosion sensitive layer. In one embodiment, the backing 21 functions as a second substrate and becomes a part of the article. In another embodiment, the backing can be removed and discarded and a second substrate can be laminated on to the now exposed surface of the adhesive 28. While Figure 3 depicts the use of a roll of tape, the method can also be practiced using cut sheets of tapes.

Figures 4A and 4B depict schematic views of another exemplary process of making an article according to the present disclosure. The process includes a step of providing a cavity 43 formed by first and second substrates 44a and 44b, which may be substantially coplanar with one another. A corrosion sensitive layer 45 is disposed on at least one of the first and second substrate. An electrical connector pad 46 lies adjacent to one of the two substrates and is in communication with the corrosion sensitive layer. For illustrative purposes, the corrosion sensitive layer is shown to be disposed on the second substrate, 44b. A delivery mechanism, such as a multi-chamber syringe 50 includes a first chamber 50a and a second chamber 50b where the components of the adhesive are stored separately. In use, one can depress a plunger in the syringe and the components will mix in a third chamber where a mixer is housed and the adhesive composition 58 can be mixed. In this way, the components can be stored under stable conditions until it is ready for use. In Figure 4b, the adhesive composition 58 has been mixed in and dispensed from the syringe and fills the cavity. After mixing, the components may be sufficiently reactive for them to polymerize and yield the final adhesive. Optionally an energy source 60, such as heat from an oven or an infrared light source can be used to cure the adhesive composition. This particular method has the advantage in that the adhesive composition, while in liquid form, can better accommodate non-uniform thickness between the first and second substrate and where the substrates are rough. This method is particularly suited for the situation where the first and second substrates are glass or a transparent substantially rigid polymeric material.

Figure 5 shows a cross-sectional view of a multi-layer article 30. The article includes a center substrate 34 having opposing first and second major surfaces, 34a and 34b respectively. On each of the first and second surfaces lies a corrosion sensitive electro-conductive layer 35. While Figure 5 shows two continuous layers 35, it is within the scope of the present disclosure to have only one layer 35 and the layer can be discontinuous. Optionally, an electrical connector pad (not shown) is attached to the substrate and the pad may be in communication with the layer 35. Covering the layers 35 are two adhesive layers 38. And, if desired, the adhesive layers can be covered with a protective liner 39.

Adhesive

The adhesives suitable for use in the present disclosure include those that are neutral or basic in nature. In other words, the adhesive preferably does not contain or contains only minor amounts of acid functionality, such that the adhesive has an acid number of less than about 5. The acid content in the adhesive does not appreciably interfere with the electrical performance of the corrosion sensitive layer over the life span of the article. The adhesive suitable for use in the present disclosure can be a pressure sensitive adhesive (PSA), a heat activated adhesive (HAA), or a cure-in-place adhesive (CIPA). In one embodiment, the adhesive is optically clear. Thus, the adhesive can be one of the following: an optically clear PSA or a non-optically clear PSA, an optically clear HAA or a non-optically clear HAA, or an optically clear CIPA or a non-optically clear CIPA.

Exemplary adhesives include polyurea, polyamide, polyurethane, polyester, addition cure silicone and combinations thereof. The adhesive has an acid number less than about 5, preferably less than 3, and more preferably less than 1. The polymers disclosed herein are typically derived from polyols or polyamines that are chain-extended with multifunctional isocyanates (to make the polyurethanes, polyureas or their combinations) or multifunctional esters (to make the polyamides, polyesters, or their combinations). Polyamides may also be derived from cyclic amides (lactams) by ring opening polymerization, but chain-extension is preferred for easy introduction of other segments. Polyesters may also be derived from polyols and multifunctional acid chlorides, provided that the acid number of less than about 5 is met. The ureas, amides, esters, or urethane groups typically provide the rigid, reinforcing segments of the polymer. Strong hydrogen bonding between these groups provides cohesive strength. In some cases, a short chain extender (typically a low molecular weight polyamine or polyol) can be used to provide additional hard segment. Optionally, the polymer may be terminated with terminal or structo-pendant curing groups, such as for example silanes, acrylates, methacrylates, residual isocyanates, epoxies, and the like. To facilitate the heat activation of the adhesives or to make them inherently tacky, soft segments derived from polyols and polyamines with lower modulus and/or lower T _g are typically preferred. Examples of these polyamines or polyols include aminopropyl functional polydimethylsiloxanes, hydroxypropyl functional polydimethylsiloxanes, polybutadiene diol, polyethylenebutylene diol, polyether diols (such as polytetrahydrofuran diol), polyether diamines (such as Jeffamine™), low T _g polyesters, and the like. Where desired, the adhesives of this invention may be further formulated with tackifϊers, and optional catalysts for the curing groups.

Preferably, the pressure sensitive adhesive has a shear elastic modulus of 3 x 10 ⁵ Pascal or lower at room temperature and has a glass transition temperature (T _g ) of about 1O ⁰ C or lower. A heat-activated adhesive typically has a for shear elastic modulus of 5 x 10 ⁵ Pascal or lower at the temperature of heat-activation and has a T _g less than the heat activation temperature. All three types of adhesive, PSA, HAA, and CIPA, whether optically clear or not, typically have both an elastic and viscous component in their modulus, i.e., the deformation (strain) of the material is not directly proportional to the applied stress and some viscous dissipation is present. The adhesive can be produced using a solvent-based solution polymerization or using bulk polymerization.

In a solution polymerization, solvent-based adhesive, the components and additives are mixed in an organic solvent, coated from solution, and then dried. When it is desired to solvent coat the adhesive, the reaction may be carried in a suitable solvent (i.e., the solvent does not interfere with the polymerization reaction) or the reaction may be carried out in bulk and the resulting polymer is dissolved in a suitable solvent for coating. Phase separation of hard and soft segments in the polymer change frequently yields a physically crosslinked network. This network provides high cohesive strength to the polymer and coating. In some cases the solvent based adhesive may be additionally cross- linked during the drying process, or in some cases it may be crosslinked after the drying step. Such crosslinkers include thermal or UV crosslinkers, which are activated during or after the drying step of preparing solvent coated adhesives. Radiation induced crosslinking such as electron beam may also be used. In addition, the polymers of the present disclosure may also include one or more curable groups. Examples of these curable groups include silanes or terminal isocyanates which are typically cured by moisture, epoxies and ethylenically unsaturated groups like acrylates, which can be cured with heat or radiation, optionally in the presence of a catalyst or initiator. The solvent- based adhesive may be coated upon suitable flexible backing materials by any known coating technique to produce adhesive coated sheet materials.

In a bulk polymerization, a monomer premix comprising the components of the adhesive are mixed using a static mixer, extruder, or a mechanical mixer to promote the reagents to come into intimate contact with each other. Optionally, a catalyst such as dibutyltindilaurate may also be added to the mixture. Bulk polymerization as described herein lends itself well for producing thick (e.g., 0.005 to 0.040 inch) adhesive films for use in rigid-to-rigid lamination applications. For example, such a thick adhesive film can be laminated to a piece of glass or be used to laminate two pieces of glasses together.

In yet another method, the components of the adhesive are mixed with the optional additives (e.g., tackifiers, thermal stabilizers, fillers) and optional crosslinker. The monomer or monomer mixture can be used in a gap-filling application, as in, e.g., filling a space between two substrates such as between two glass substrates. In one application, a syringe is used to deliver the adhesive components into the gap, and the reagent is cured using thermal radiation. Such a method and delivery mechanism is well suited for gaps with varying thicknesses or where the substrates have surfaces that are not substantially flat.

The flexible backing materials may be any materials conventionally used as a tape backing, optical film, release liner or any other flexible material. When the final product application requires adhesive contact with the corrosion sensitive surface but is outside of the optical path, the backing does not have to be optically clear. Typical examples of flexible backing materials used as tape backing that may be useful for the adhesive compositions include those made of plastic films such as polypropylene, polyethylene, polyurethane, polyvinyl chloride, polyester (e.g., polyethylene terephthalate), cellulose acetate, and ethyl cellulose. Some flexible backing may have coatings. For example a release liner may be coated with a low adhesion component, such as silicone. Illustrative coating techniques include roll coating, spray coating, knife coating, die coating, printing, and the like. Solution processing as described herein lends itself well for producing thin e.g. 25 to 75 micron (0.001 to 0.003 inch) adhesive films for use as transfer tapes. The resulting tape has low volatile residuals after oven drying.

Examples

These examples are merely for illustrative purposes only and are not meant to be limiting on the scope of the appended claims. All parts, percentages, ratios, etc. in the examples and the rest of the specification are by weight, unless noted otherwise. Solvents and other reagents used were obtained from Sigma-Aldrich Chemical Company; Milwaukee, Wisconsin unless otherwise noted.

Haze and Transmission Testing

A 25 micron thick sample of the adhesive was laminated to a 25 micron thick Melinex ^® polyester film 454 (from DuPont Company, Wilmington, DE) in a manner so as to assure that no air bubbles are trapped between the film and the adhesive layer. A 75mm by 50 mm plain micro slide (a glass slide from Dow Corning, Midland, MI), that had been wiped three times with isopropanol, was laminated to the adhesive sample using a hand roller to assure no air bubbles were trapped between the adhesive and the glass slide. The percent (%) transmission and haze were measured using a Model 9970 BYK Gardner TCS Plus Spectrophotometer (from BYK Gardner, Columbia, MD). The background measurement was made with a sandwich of the Melinex ^® polyester film 454 and the glass slide. The % transmission and the haze of the adhesive sample were then obtained directly on the film/adhesive/glass laminate in the spectrophotometer.

Each of the adhesives of Examples 1 to 5 had an optical transmission value greater than 90% and a haze value below 5%.

ITO Compatibility Study of Corrosion Sensitive Layer

The compatibility of the adhesive with the corrosion sensitive layer, which was a layer of indium-tin-oxide (ITO), was done as follows. A sample of the adhesive was transferred to a 0.0015 inch thick primed polyester (PET) backing to form a tape. The tape was then laminated to a PET film having a major surface coated with ITO layer such that the adhesive was in direct contact with the traces to from a laminate. An initial surface resistance was measured on the ITO trace using an ohm meter where electrical leads of the meter are placed across the connector pads. The resulting laminate was conditioned in an oven set at 60 ⁰ C and 90% relative humidity. The surface resistance for each sample was measured periodically over a period of 28 days using an ohm meter. An average of five surface resistance measurements was recorded.

A control sample included an ITO trace exposed to ambient conditions, i.e., no adhesive was laminated onto the PET substrate having the ITO containing trace.

Compatibility Testing with Other Corrosion Sensitive Surfaces

The compatibility of the adhesive with the corrosion sensitive material, which was a nickel or aluminum vapor metallized PET, was done as follows. A sample of the adhesive was transferred to a 0.0015 inch thick primed polyester (PET) backing to form a tape. The tape was then laminated to the metallized PET film such that the adhesive was in direct contact with the nickel or aluminum. Initial light transmittance and Delta(E) of the laminates were measured using a Model 9970 BYK Gardner TCS Plus Spectrophotometer (from BYK Gardner, Columbia, MD). The resulting laminate was conditioned in an oven set at 60 ⁰ C and 90% relative humidity and the light transmittance and Delta(E) for each sample were measured periodically over a period of 25 days. Delta(E) is used to describe (mathematically) the distance between two colors. It is defined as the square -root of the sum of (Li-L ₂ ) ² , (ai_a ₂ ) ² , and (bi-b ₂ ) ² , where L, a, and b are color indexes.

Example 1

Into a reactor was charged 800 grams Jeffamine ^® D-2000 polyetheramine (from Huntsman Corp., The Woodlands, Texas), 800 grams isopropanol, 22.35 grams Dytek ^® A diamine (from DuPont, Wilmington, Delaware), and 151.36 grams Desmodur ^® W monomeric cycloaliphatic diisocyanate (from Bayer Material Science AG, Leverkusen, Germany) dissolved in 600 grams isopropanol. The resulting mixture was placed on a mechanical roller at room temperature for 48 hours. The solution was then coated on a siliconized polyester release liner and dried at 7O ⁰ C for 10 minutes to a final pressure sensitive polyamide -based adhesive with a thickness of 25 microns (0.001 inch). Example 2

Into a reactor was charged 86 grams hydroxyl functionalized polybutadiene with a number average molecular weight of 2,800 (CAS number 69102-90-5, available from Aldrich, Milwaukee, Wisconsin) with 9.15 grams isophorone diisocyanate (0.08 equivalents). The resulting mixture was allowed to react under a dry nitrogen atmosphere for 2 hours at 8O ⁰ C. Thereafter, 5.3 grams aminopropyl trimethoxysilane (0.21 equivalents) was added. The mixture was stirred for 10 minutes and then 66.7 grams of toluene was added to produce a 60% solids solution of silane terminated urethane. The solution was coated onto a liner and dried at 7O ⁰ C for 15 minutes to a final pressure sensitive thickness of 48 microns (0.0019 inch). Due to the presence of the terminal trimethoxy silane groups, this dry polymer coating can continue to cure in the presence of moisture to yield a crosslinked polymer coating. Moisture curing can be accelerated in the presence of a catalyst such as dibutyl tin dilaurate.

Example 3

Into a reactor was charged 150 grams of Priplast ^® 3192, semicrystalline polyester polyol (1020 hydroxyl equivalent weight, 0.147 equivalents, from Uniqema, New Castle, Delaware) and 27.7 grams isophorone diisocyanate (0.25 equivalents). The resulting mixture was allowed to react under a dry nitrogen atmosphere for 2 hours at 8O ⁰ C. Thereafter, 22.3 grams aminopropyl trimethoxysilane (0.10 equivalents) was added. The mixture was stirred for 10 minutes and then 66.7 grams of toluene was added to produce a 75% solids solution of silane terminated urethane. The solution was coated onto a liner and dried at 7O ⁰ C for 15 minutes to a final pressure sensitive thickness of 38 microns (0.0015 inch). Like the material of Example 2, this polymer can also be crosslinked in the presence of moisture. Table 1 Components for Examples 4 and 5

Preparative Example A: Synthesis of Silicone Polyurea (SPU) Elastomer

In a reaction vessel PDMS diamine 33,000, DYTEK A, and H12MDI were charged in a mole ratio of 1 :1 :2 in a sufficient amount of 2-propanol to give a 20% solids solution of the reagents. The mixture was stirred for 2 hours to give a silicone polyurea elastomer at 20% solids.

Preparative Example B

A sample of 14K PDMS diamine (830.00 grams) was placed in a 2 liter, 3-neck resin flask equipped with a mechanical stirrer, heating mantle, nitrogen inlet tube (with stopcock), and an outlet tube. The flask was purged with nitrogen for 15 minutes and then, with vigorous stirring, diethyl oxalate (33.56 grams) was added dropwise. This reaction mixture was stirred for approximately one hour at room temperature and then for 75 minutes at 8O ⁰ C. The reaction flask was fitted with a distillation adaptor and receiver. The reaction mixture was heated under vacuum (133 Pascals, 1 Torr) for 2 hours at 12O ⁰ C and then for 30 minutes at 13O ⁰ C, until no further distillate was able to be collected. The reaction mixture was cooled to room temperature to provide an oxamido ester terminated silicone product (i.e., the silicone diamine is terminated on both ends with monoethyl oxamide ester groups). Gas chromatographic analysis of the clear, mobile liquid showed that no detectable amount of diethyl oxalate remained. The ester equivalent weight of this precursor for preparative example C was determined by titration (equivalent weight = 8,272 grams/equivalent).

Titration Method to Determine Equivalent Weight

Approximately 10 grams of the precursor compound of preparative example B was added to a jar. Approximately 50 grams THF solvent was added. The contents were mixed using a magnetic stir bar mix until the mixture was homogeneous. The theoretical equivalent weight of precursor was calculated and then an amount of N-hexylamine in the range of 3 to 4 times this number of equivalents was added. The reaction mixture was stirred for a minimum of 4 hours. Bromophenol blue (10-20 drops) was added and the contents were mixed until homogeneous. The mixture was titrated to a yellow endpoint with 1.0N (or 0.1N) hydrochloric acid. The number of equivalents of precursor was equal to the number of equivalents of N-hexylamine added to the sample minus the number of equivalents of hydrochloric acid added during titration. The equivalent weight (grams/equivalent) was equal to the sample weight of the precursor divided by the number of equivalents of the precursor.

Preparative Example C

The precursor of Preparative Example B (98.13 grams) and ethylene diamine (0.36 grams) were weighed into a jar. The jar was sealed and the mixture was rapidly agitated until the contents became too viscous to flow. The jar was placed on a roller mill overnight at ambient temperature. The solid product was collected.

Example 4

For Example 4, the silicone polyurea elastomer adhesive was prepared by blending the silicone polyurea elastomer (80 parts) from Preparative Example A with Additive Oil (20 parts) using conventional solvent means, at 20% solids in a solvent blend of IPA (120.00 parts), 30 % by weight and toluene, (280.00 parts) 70 % by weight. These samples were coated from the solvent mixture onto Primed PET and dried to 25 micron final thickness.

Example 5

The copolymer of Preparative Example C (18.50 grams) was dissolved in THF (45.60 grams). MQ Resin (30.83 grams, 60.0% solids) was added to the polymer solution. The resulting mixture was mixed overnight at ambient conditions and then knife coated onto PET. The coated film was dried for about 15 minutes at ambient temperature followed by 10 minutes in a 13O ⁰ C oven, to yield a 25 micron dry thickness coating.

Figure 5 shows the compatibility study of the adhesives of Examples 1 to 5 and a Control sample over a 28 day period as described in the test method recited above. As the data shows, all five samples exhibited 20% or less increase in resistance after 28 days exposure 6O ⁰ C and 90% relative humidity (RH), well within the target of less than 20% electrical resistance change in 21 days exposure. While the Control sample showed the smallest increase in resistance as compared to the examples, in use for product devices contemplated herein, an adhesive will be required.

Example 6

The adhesive of Example 5 (25 micron) was laminated to both sides of a polyolefm (ExxonMobil EXACT 8210) carrier film (125 mil) to yield a adhesive transfer tape, with a polyolefm core and silicone adhesive surfaces.

Tables 2 and 3 show the compatibility studies of the adhesives of Example 6 on nickel and aluminum vapor metallized PET films. The data show minimum corrosion of the metallic surfaces by the adhesive as indicated by comparable increase of transmittance and Delta(E). Table 2

Transmittance measurement of metal coated PET films after exposure at

60°C/90%RH

Table 3 Delta(E) measurement of metal coated PET films after exposure at 60°C/90%RH

Example 7

Two silicone adhesives, Dow Corning 7657 and Dow Corning 7658 (70/30 dry- weight ratio), were mixed with Dow Corning Syl-Off 7678 crosslinker (0.16 parts) and the Dow Corning Syl-Off 4000 catalyst. The mixed solution was dried on a fluorosilicone liner for about 15 minutes in a 13O ⁰ C oven to yield a 36 micron dry thickness coating. The dried adhesive was then laminated to both sides of a polyolefin (ExxonMobil EXACT 8210) carrier film (100 mil) to yield an adhesive transfer tape.

Table 4 displays the surface resistance change when the adhesive of Example 7 was placed on an ITO surface. The data shows minimum ITO corrosion as indicated by the small increase in resistance.

Table 4 Surface resistance change after ITO film exposure at 60°C/90%RH