Patent Application
20150275040
Touch screens are commonly found in consumer, commercial, and industrial systems. A touch screen allows a user to control various aspects of a system by touch or gestures directly on the touch screen itself For example, a user may interact with one or more objects depicted on a display device by touch or gestures that are sensed by a touch sensor. Typically, the touch sensor includes a conductive pattern disposed on a substrate that is configured to sense touch. Touch sensors are prone to damage such as, for example, scratching and breakage, due to the increased level of direct contact. As a consequence, touch screens typically include a transparent cover lens that overlays the touch sensor to protect the underlying components from environmental conditions, chemical agents, abrasion, and oxidation.
However, the transparent cover lens is conventionally composed of polyester or glass. While flexible, polyester can only provide a minimal level of hardness. For example, a transparent cover lens composed of polyester provides a pencil hardness in a range between HB and 4H that is susceptible to scratching and other failure modes. Glass provides improved hardness at the expense of flexibility. For example, a transparent cover lens composed of glass provides increased pencil hardness compared to polyester, but is inflexible and is susceptible to breakage and other failure modes.
According to one aspect of one or more embodiments of the present invention, a radiation-curable hard-coat composition includes a principal resin that includes multi-(meth)acrylate functionalized oligomers or polymers and a free radical-polymerization initiator. The initiator includes at least two photo-initiators in a predetermined ratio that generate a highly reactive species when irradiated with radiation.
Other aspects of the present invention will be apparent from the following description and claims.
One or more embodiments of the present invention are described in detail with reference to the accompanying figures. For consistency, like elements in the various figures are denoted by like reference numerals. In the following detailed description of the present invention, specific details are set forth in order to provide a thorough understanding of the present invention. In other instances, well-known features to one of ordinary skill in the art are not described to avoid obscuring the description of the present invention.
In one or more embodiments of the present invention, a radiation-curable hard-coat 160 may be used on a top, or user-facing side, of transparent cover lens (e.g., 150 of
In one or more embodiments of the present invention, a radiation-curable hard-coat 160 may be used instead of a transparent cover lens (e.g., 150 of
Touch screen enabled system 200 may include one or more printed circuit boards or flexible circuits (not shown) on which one or more processors (not shown), system memory (not shown), and other system components (not shown) may be disposed. Each of the one or more processors may be a single-core processor (not shown) or a multi-core processor (not shown) capable of executing software instructions. Multi-core processors typically include a plurality of processor cores disposed on the same physical die (not shown) or a plurality of processor cores disposed on multiple die (not shown) disposed within the same mechanical package (not shown). System 200 may include one or more input/output devices (not shown), one or more local storage devices (not shown) including solid-state memory, a fixed disk drive, a fixed disk drive array, or any other non-transitory computer readable medium, a network interface device (not shown), and/or one or more network storage devices (not shown) including a network-attached storage device or a cloud-based storage device.
In certain embodiments, touch screen 100 or 102 may include touch sensor 130 that overlays at least a portion of a viewable area 230 of display device 110. Touch sensor 130 may include a viewable area 240 that corresponds to that portion of the touch sensor 130 that overlays the light emitting pixels (not shown) of display device 110 (e.g., viewable area 230 of display device 110). Touch sensor 130 may include a bezel circuit 250 outside at least one side of the viewable area 240 that provides connectivity between touch sensor 130 and a controller 210. In other embodiments, touch sensor 130, or the function that it implements, may be integrated into display device 110 (not independently illustrated). Controller 210 electrically drives at least a portion of touch sensor 130. Touch sensor 130 senses touch (capacitance, resistance, optical, acoustic, or other technology) and conveys information corresponding to the sensed touch to controller 210.
The manner in which the sensing of touch is measured, tuned, and/or filtered may be configured by controller 210. In addition, controller 210 may recognize one or more gestures based on the sensed touch or touches. Controller 210 provides host 220 with touch or gesture information corresponding to the sensed touch or touches. Host 220 may use this touch or gesture information as user input and respond in an appropriate manner. In this way, the user may interact with touch screen enabled system 200 by touch or gestures on touch screen 100 or 102. In certain embodiments, host 220 may be the one or more printed circuit boards (not shown) or flexible circuits (not shown) on which the one or more processors (not shown) are disposed. In other embodiments, host 220 may be a subsystem (not shown) or any other part of system 200 (not shown) that is configured to interface with display device 110 and controller 210. One of ordinary skill in the art will recognize that the components and the configuration of the components of touch screen enabled system 200 may vary based on an application or design in accordance with one or more embodiments of the present invention.
In certain embodiments, controller 210 may interface with touch sensor 130 by a scanning process. In such an embodiment, controller 210 may electrically drive a selected row channel 320 (or column channel 310) and sample all column channels 310 (or row channels 320) that intersect the selected row channel 320 (or the selected column channel 310) by sensing, for example, changes in capacitance. The change in capacitance may be used to determine the location of the touch or touches. This process may be continued through all row channels 320 (or all column channels 310) such that changes in capacitance are measured at each uniquely addressable location of touch sensor 130 at predetermined intervals. Controller 210 may allow for the adjustment of the scan rate depending on the needs of a particular application or design. In other embodiments, controller 210 may interface with touch sensor 130 by an interrupt driven process. In such an embodiment, a touch or a gesture generates an interrupt to controller 210 that triggers controller 210 to read one or more of its own registers that store sensed touch information sampled from touch sensor 130 at predetermined intervals. One of ordinary skill in the art will recognize that the mechanism by which touch or gestures are sensed by touch sensor 130 and sampled by controller 210 may vary based on an application or a design in accordance with one or more embodiments of the present invention.
One of ordinary skill in the art will recognize that other touch sensor 130 stackups (not shown) may be used in accordance with one or more embodiments of the present invention. For example, single-sided touch sensor 130 stackups may include conductors disposed on a single side of a substrate 410 where conductors that cross are isolated from one another by a dielectric material (not shown), such as, for example, as used in On Glass Solution (“OGS”) touch sensor 130 embodiments. Double-sided touch sensor 130 stackups may include conductors disposed on opposing sides of the same substrate 140 (as shown in
A conductive pattern 420 or 430 may be disposed on one or more transparent substrates 410 by any process suitable for disposing conductive lines or features on a substrate. Suitable processes may include, for example, printing processes, vacuum-based deposition processes, solution coating processes, or cure/etch processes that either form conductive lines or features on substrate or form seed lines or features on substrate that may be further processed to form conductive lines or features on substrate. Printing processes may include flexographic printing processes, including the flexographic printing of a catalytic ink that may be metallized by an electroless plating process to plate a metal on top of the printed catalytic ink or direct flexographic printing of conductive ink or other materials capable of being flexographically printed, gravure printing, inkjet printing, rotary printing, or stamp printing. Deposition processes may include pattern-based deposition, chemical vapor deposition, electro deposition, epitaxy, physical vapor deposition, or casting. Cure/etch processes may include optical or Ultra-Violet (“UV”)-based photolithography, e-beam/ion-beam lithography, x-ray lithography, interference lithography, scanning probe lithography, imprint lithography, or magneto lithography. One of ordinary skill in the art will recognize that any process or combination of processes, suitable for disposing conductive lines or features on substrate, may be used in accordance with one or more embodiments of the present invention.
With respect to transparent substrate 410, transparent means capable of transmitting a substantial portion of visible light through the substrate suitable for a given touch sensor application or design. In typical touch sensor applications, transparent means transmittance of at least 85 percent of incident visible light through the substrate. However, one of ordinary skill in the art will recognize that other transmittance values may be desirable for other touch sensor applications or designs. In certain embodiments, transparent substrate 410 may be polyethylene terephthalate (“PET”), polyethylene naphthalate (“PEN”), cellulose acetate (“TAC”), cycloaliphatic hydrocarbons (“COP”), polymethylmethacrylates (“PMMA”), polyimide (“PI”), bi-axially-oriented polypropylene (“BOPP”), polyester, polycarbonate, glass, copolymers, blends, or combinations thereof. In other embodiments, transparent substrate 410 may be any other transparent material suitable for use as a touch sensor substrate. One of ordinary skill in the art will recognize that the composition of transparent substrate 410 may vary based on an application or design in accordance with one or more embodiments of the present invention.
In certain embodiments, the first plurality of parallel conductive lines oriented in the first direction 505 may be perpendicular (not shown) to the first plurality of parallel conductive lines oriented in the second direction 510, thereby forming a rectangle-type mesh (not shown). In other embodiments, the first plurality of parallel conductive lines oriented in the first direction 505 may be angled relative to the first plurality of parallel conductive lines oriented in the second direction 510, thereby forming a parallelogram-type mesh. One of ordinary skill in the art will recognize that the relative angle between the first plurality of parallel conductive lines oriented in the first direction 505 and the first plurality of parallel conductive lines oriented in the second direction 510 may vary based on an application or a design in accordance with one or more embodiments of the present invention.
In certain embodiments, a first plurality of channel breaks 515 may partition first conductive pattern 420 into a plurality of column channels 310, each electrically isolated from the others (no electrical continuity). One of ordinary skill in the art will recognize that the number of channel breaks 515, the number of column channels 310, and/or the width of the column channels 310 may vary based on an application or design in accordance with one or more embodiments of the present invention. Each column channel 310 may route to a channel pad 540. Each channel pad 540 may route via one or more interconnect conductive lines 550 to an interface connector 560. Interface connectors 560 may provide a connection interface between a touch sensor (e.g., 130 of
In certain embodiments, the second plurality of parallel conductive lines oriented in the first direction 520 may be perpendicular (not shown) to the second plurality of parallel conductive lines oriented in the second direction 525, thereby forming a rectangle-type mesh (not shown). In other embodiments, the second plurality of parallel conductive lines oriented in the first direction 520 may be angled relative to the second plurality of parallel conductive lines oriented in the second direction 525, thereby forming a parallelogram-type mesh. One of ordinary skill in the art will recognize that the relative angle between the second plurality of parallel conductive lines oriented in the first direction 520 and the second plurality of parallel conductive lines oriented in the second direction 525 may vary based on an application or a design in accordance with one or more embodiments of the present invention.
In certain embodiments, a plurality of channel breaks 530 may partition second conductive pattern 430 into a plurality of row channels 320, each electrically isolated from the others (no electrical continuity). One of ordinary skill in the art will recognize that the number of channel breaks 530, the number of row channels 320, and/or the width of the row channels 320 may vary based on an application or design in accordance with one or more embodiments of the present invention. Each row channel 320 may route to a channel pad 540. Each channel pad 540 may route via one or more interconnect conductive lines 550 to an interface connector 560. Interface connectors 560 may provide a connection interface between a touch sensor (e.g., 130 of
In certain embodiments, the first conductive pattern 420 may include a first plurality of parallel conductive lines oriented in a first direction (e.g., 505 of
In certain embodiments, one or more of the plurality of parallel conductive lines oriented in the first direction (e.g., 505 of
Conventional coating compositions for protective applications that require some measure of scratch and abrasion resistance typically employ a cross-linked polymer-based molecular structure. A cross-link is a bond, covalent or ionic, that links one monomer or polymer to another. Cross-linked polymer structures are linked together in a three-dimensional structure that increases the intermolecular forces, usually covalent bonds, within the polymer chains and limits polymeric chain relaxation. Compared to a linear polymer structure, where monomers with dual functional groups are joined together in a chain, the scratch resistance of a cross-linked polymer may be dictated by the cross-linking density. The cross-linking density refers to the percentage of cross-linked bonds within a given polymer.
While cross-linked polymer structures provide improved scratch resistance over linear polymer structures, the use of conventional coatings based on cross-linked polymer structures presents a number of issues that impede their effective use. Conventional coating compositions typically require a choice, or at least a compromise, between flexibility and hardness. In applications or designs that require a high degree of hardness for scratch resistance, the applied coating tends to be inflexible, brittle, and susceptible to breakage. Alternatively, in applications or designs that require a high degree of flexibility to resist breakage, the applied coating is prone to scratching. In addition, conventional coating compositions typically exhibit shrinkage after curing by, for example, exposure to radiation. In applications or designs that apply the coating to substrates with low mechanical strength, such as flexible PET substrates used in touch sensor applications, the shrinkage of the cured coating gives rise to undesirable curling of the flexible substrate.
In addition, conventional coating compositions are difficult to apply for a number of reasons. While a uniform and consistent coating may be obtained through a solution deposition process, crosslinked polymers cannot be dissolved in any solvent. As such, while it is desirable to apply the coating composition in a liquid state, it is necessary to form the high density of cross-linking after the curing process of the liquid coating composition to the substrate. Thus, the density of cross-linking is constrained by the effectiveness of the curing process after application of the coating to the substrate. Moreover, the application of conventional coating compositions may not be possible, or is at least made very difficult, using conventional solution-based application processes. This is due to the fact that cross-linked polymers cannot dissolve in any solvent and swell when placed in solvent. This is problematic because coating compositions typically have to be in a liquid state to allow molecules to move and react in an efficient manner. As such, conventional coating compositions require trade-offs in various properties that render the coating at least inefficient, at worst inoperable for their intended purpose, increase the difficulty and cost of manufacturing, and negatively impact yield.
To that end, UV-curable coating compositions, containing a (meth)acrylate compound as a principal resin, have been used as protective films because the cured coating provides some manner of transparency, mechanical strength, and scratch resistance. Conventionally, UV-curable coating compositions are composed of a cation radiation curable resin and a cation polymerization initiator which generates a cation when irradiated with UV radiation. In some cases, inorganic particles are included to increase the mechanical strength, pencil hardness, and scratch resistance. In contrast, radical-polymerization coating compositions have received less attention because they are difficult to process and cure. Specifically, in thin-film applications of UV-curable coating compositions, curing effectiveness is inhibited by the presence of oxygen and nitrogen sealing or the like may be required to cure at some level of effectiveness. While progress has been made in developing UV-curable coating compositions based on radical-polymerization mechanisms, a number of issues continue to impede their widespread adoption and use. For example, conventional UV-curable coating compositions based on radical-polymerization possess high internal stress due to the fast curing process and the high internal stress leads to lack of flexibility.
Accordingly, in one or more embodiments of the present invention, a radiation-curable hard-coat composition provides a transparent hard coat that provides well-balanced flexibility and hardness, a high degree of scratch and abrasion resistance, and improved adhesiveness, UV stability, and process-ability in a manufacturing environment, including, for example, touch sensor applications. The radiation-curable hard-coat composition facilitates all aspects of manufacturing including application, processing, and post-fabrication processing and improves yield while reducing costs.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition is a coating that, when cured by radiation, forms a three-dimensional cross-linked network through a free-radical polymerization mechanism. The radiation-curable hard-coat composition includes a principal resin that includes multi-(meth)acrylate functionalized oligomers or polymers and a free radical-polymerization initiator, as a curing agent, that generates a highly reactive species when exposed to radiation. The photo-initiators contains multiple components including at least two curing agents in a predetermined ratio, such as, for example, one or more surface curing agents and one or more deep curing agents that improve curing efficiency and provide homogenous curing along the depth of the applied coating. In addition, a solvent may optionally be included that enables the manufacture of the radiation-curable hard-coat composition in a manner that is fast, efficient, and cost effective to apply, process, and process post-fabrication.
As the principal resin, a multi-(meth)acrylate functionalized oligomers or polymers resin may be used as a film-forming component, which imparts the basic properties of the cured coating. Compared to small molecules, oligomers or polymers are relatively large molecules which are obtained by chemically linking tens to thousands of relatively small molecules. Specifically, multi-(meth)acrylate functionalized oligomers or polymers typically have a molecular weight in a range between 500 and 20,000 and possess between 2 and 15 acrylate functional groups per molecule. As a result, a high degree of cross-linking may be achieved for improved hardness. The multi-(meth)acrylate functionalized oligomers or polymers may be derived from various chemical backbones, such as, for example, polyol, polyester, polyurethane, polyether, epoxies, and acrylics. In terms of molecular geometry, they may be linear or branched. Because of the skeleton of the resin backbone and the molecular geometry, these multi-(meth)acrylate functionalized oligomers or polymers are highly viscous liquids with a viscosity in a range between at least a few thousand centipoises and potentially greater than one million centipoises in a broad temperature window.
Pentaerithritol tetraacrylate(“PETA”) is a commonly used UV-curable resin because it provides a high degree of cross-linking in the cured coating due to the relatively large ratio of (meth)acrylate functionality over the molecular weight. As such, it has been employed for protective coatings in various applications, including display applications where it provides a high degree of scratch resistance. However, PETA resins exhibit significant volumetric shrinkage during curing due to its intrinsic molecular structure. This presents a number of issues including, for example, a high degree of undesirable curling and brittleness. In contrast, a radiation-curable hard-coat composition that includes multi-(meth)acrylate functionalized oligomers or polymers as a principal resin may use a limited amount of PETA, if it uses any at all, as a complimentary component to provide additional cross-linking density. Because of the unique molecular characteristics noted herein, the multi-(meth)acrylate functionalized oligomers or polymers exhibit a substantially smaller amount of shrinkage, less than 5 percent by volume, after radiation curing. As such, a low level of built-in stress is induced in the coating resulting in a small curling angle after radiation curing. In addition, because of the multi-functionality of the (meth)acrylate functionalized oligomers or polymers used, the cross-linking density is very high after curing. In one or more embodiments of the present invention, in a radiation-curable hard-coat composition, the principal resin content as a percentage of weight of the composition may be in a range between 5 percent and 96 percent.
The cross-linking density of cross-linked polymers may be dictated by the effectiveness of the radiation curing. As such, photo-initiators play a critically important role in a radiation-curable coating composition. A photo initiator is a compound especially added to a composition to convert absorbed light energy, UV radiation or visible light, or other radiation into chemical energy in the form of an initiating species, such as, for example, free radicals. The free radical-polymerization initiator of the radiation-curable hard-coat composition includes at least two photo-initiators that generate a free radical when irradiated with radiation to initiate polymerization. The photo-initiators may include, but are not limited to, acetophenone, anisoin, anthraquinone, anthraquinone-2-sulfonic acid, sodium salt monohydrate, (benzene) tricarbonylchromium, benzil, benzoin, benzoin ethyl ether, benzoin isobutyl ether, benzoin methyl ether, benzophenone, benzophenone/1-hydroxycyclohexyl phenyl ketone, 50/50 blend, 3,3′,4,4′-benzophenonetetracarboxylic dianhydride, 4-benzoylbiphenyl, 2-benzyl-2-(dimethylamino)-4′-morpholinobutyrophenone, 4,4′-bis(diethylamino)benzophenone, 4,4′-bis(dimethylamino)benzophenone, camphorquinone, 2-chlorothioxanthen-9-one, dibenzosuberenone, 2,2-diethoxyacetophenone, 4,4′-dihydroxybenzophenone, 2,2-dimethoxy-2-phenylacetophenone, 4-(dimethylamino)benzophenone, 4,4′-dimethylbenzil, 2,5-dimethylbenzophenone, 3,4-dimethylbenzophenone, diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide/2-hydroxy-2-methylpropiophenone, 50/50 blend, 4′-ethoxyacetophenone, 2,4,6-trimethylbenzoyldiphenylphophine oxide, phenyl bis(2,4,6-trimethyl benzoyl)phosphine oxide, 2-ethylanthraquinone, ferrocene, 3′-hydroxyacetophenone, 4′-hydroxyacetophenone, 3-hydroxybenzophenone, 4-hydroxybenzophenone, 1-hydroxycyclohexyl phenyl ketone, 2-hydroxy-2-methylpropiophenone, 2-methylbenzophenone, 3-methylbenzophenone, methybenzoylformate, 2-methyl-4′-(methylthio)-2-morpholinopropiophenone, phenanthrenequinone, 4′-phenoxyacetophenone, and others.
In one or more embodiments of the present invention, in a radiation-curable hard-coat composition, the free radical-polymerization initiator content as a percentage of weight of the composition may be in a range between 0.5 percent and 8.0 percent, preferably in a range between 2.0 percent and 5.0 percent. Due to the spectral interference between different photo-initiators, the ratio of at least two combined photo-initiators has been quantitatively investigated and optimized with an overall photo-initiator content of 4.5 percent by weight of the composition. The samples were measured for curing characteristics in photo-assisted Differential Scanning Calorimetry (“DSC”) using DSC-Q2000 by TA Instruments. Light from a 100-W high pressure mercury lamp was used. The light intensity was determined by placing an empty DSC pan on the sample cell. The light intensity was 80 mW/cm2 over a wavelength range between 320 nanometers and 500 nanometers. Photopolymerization was carried out at 25° C. in a nitrogen atmosphere.
These plots show the enthalpy value and the curing time of the representative coating compositions. As shown in plot A, approximately 35 percent of the photo-initiator was consumed in the first irradiation cycle (0.6 seconds for each irradiation cycle) and two additional irradiation cycles were needed to initiate the curing agent up to 90 percent. As shown in plot B, there was an improvement in effectiveness of the curing in the first irradiation cycle as approximately 65 percent of photo-initiator was excited in the first irradiation cycles. This suggests that the use of multi-constituent photo-initiators may be more effective than a mono-constituent photo-initiator. As the ratio of diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide was reduced, the photo-initiating efficiency improved to consume more than 80 percent of the photo-initiator in the first irradiation cycle as shown in plot C and plot D. This result suggests that absorption spectrum interference between different photo-initiators is an important criterion in designing a multi-constituent photo-initiator for efficient curing in a minimal irradiation dose. Thus, at least two different photo-initiators, such as, for example, one for deep curing and another for surface curing, may be combined to provide sufficient cross-linking efficiency under the same irradiation exposure. This is critically important in the case of thick films of hard coat having a thickness of 10 micrometers or more.
As discussed above, cross-linked polymer materials typically cannot be directly applied or coated onto a substrate or screen through a solution-based application process because the cross-linked polymers are not dissolvable in any solvent and only swell when placed in the solvent. Coating compositions are typically provided in the liquid state to allow the molecules to move and react more efficiently. However, in many applications, a solvent is employed in the coating compositions to provide a cost-effective solution process and other property adjustments including viscosity. In this regard, the solvent is an important component of the coating composition as it plays a critically important role in determining viscosity, film thickness, coating quality, and baking process parameters for effective solvent removal. The solvent content may depend on the coating method used, the desired coating thickness, and the properties of the finished coating product. The coating composition may contain solid content in a range between 10 percent by weight and 80 percent by weight of the composition, and in some applications, solvent content in a range between 20 percent by weight and 30 percent by weight of the composition to regulate viscosity.
As discussed above, radiation-curable hard-coat composition that includes a principal resin of multi-end-capped (meth)acrylate functionalized oligomers or polymers have a large molecular weight in a range between 500 and 20,000 and between 2 and 15 acrylate functional groups per molecule. When put in a solvent, the oligomers and polymers may potentially aggregate in micro scale due to the entanglement of random-coil chains of polymers. This presence of micro-aggregation results in inconsistencies in the coating quality and sacrifices optical quality giving rise to low transmission and high haze. A desirable solvent for the radiation-curable hard-coat composition includes the ability to dissolve coating resins under acceptable conditions for production, provide suitable coating quality, provide acceptable tolerance for manufacturing to a target film thickness based on the slope of viscosity versus solid content, and fast drying rate to ensure complete evaporation of solvent during the soft-bake phase. The soft-bake phase is the physical process between the deposition of the coating on a substrate and radiation curing in which a liquid-cast resin is converted to a relative solid film through solvent evaporation. In some cases, a temperature controlled oven channel may be employed to ensure the complete elimination of added solvents because any residual solvent may adversely affect the curing and the scratch resistance properties of the coating.
In one or more embodiments of the present invention, solvents that may optionally be used in the radiation-curable hard-coat composition may include, but are not limited to, ketone-type solvents (both acyclic ketones and cyclic ketones), such as acetone, methyl ethyl ketone, iso-butyl ethyl ketone and cyclopentanone, cyclohexanone, as well as alcohol-type solvents such as ethoxy ethanol, methoxy ethanol, and 1-methoxy-2-propanol. The use of cyclopentanone advantageously tends to minimize air bubbles trapped in the coating after application. In addition, the reduction of trapped air bubbles improves cross-linking induced during radiation curing. Air bubbles tend to contain approximately 21 percent oxygen by volume and the oxygen tends to quench the free radicals. Moreover, co-solvents of two or more solvents may be applied as the coating carrier. The large variety of solvents enables flexibility in tuning the viscosity of the radiation-curable hard-coat composition for various coating techniques including, for example, inkjet printing, spray coating, slot-die coating, dip-coating, curtain coating, gravure coating, and reverse-gravure coating. One of ordinary skill in the art will recognize that other coating techniques may be used in accordance with one or more embodiments of the present invention.
In one or more embodiments of the present invention, various combinations of the above-noted components may be used to create a radiation-curable hard-coat composition that exhibit different degrees of the various characteristics of the coating composition. While a few exemplary combinations are provided herein, one of ordinary skill in the art, having the benefit of this disclosure, will recognize that other combinations may be used in accordance with one or more embodiments of the present invention.
In certain embodiments, a radiation-curable hard coat composition may include a principal resin comprising multi-(meth)acrylate functionalized oligomers or polymers and a free radical-polymerization initiator comprising at least two photo-initiators in a predetermined ratio that generate a highly reactive species when irradiated with radiation. The principal resin may comprise aliphatic urethane acrylate content in a range between 5 percent and 90 percent as a percentage of weight of the composition and PETA content in a range between 0 percent and 70 percent as a percentage of weight of the composition. The free radical-polymerization initiator may comprise initiator content in a range between 1 percent and 5 percent as a percentage of weight of the composition to absorb shorter wavelengths, that has maximum absorption in a range between 200 nanometers and 300 nanometers such as, for example, 1-hydroxycyclohexyl phenyl ketone, and initiator content in a range between 0.5 percent and 4 percent as a percentage of weight of the composition to absorb longer wavelengths, that has absorption in a range between 300 nanometers and 420 nanometers, such as, for example, diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide, where for the examples given, the predetermined ration is 4-to-1. In one or more embodiments of the present invention, the predetermined ratio of the first initiator to the second initiator is in a range between 5-to-1 and 2-to-1. A solvent comprising 1-methoxy-2-propanol content in a range between 10 percent and 80 percent as a percentage of weight of the composition. The coating composition was deposited on PMMA and PET substrates followed by UV radiation curing to achieve hard-coat films with a thickness ranging from 5 micrometers to 20 micrometers. The applied hard coat exhibited high pencil hardness (8H to 9H for PMMA substrate and 4H to 6H for PET substrate) with a loading of 750 grams based on ASTM D-3363 test, excellent abrasion resistance with no obvious scratch after 1000 cycles of steel-wool test with a loading of 750 grams based on ASTM F-2357 test, and excellent adhesion of 5B based on ASTM D-3359 test.
In other embodiments, a radiation-curable hard coat composition may include a principal resin comprising multi-(meth)acrylate functionalized oligomers or polymers and a free radical-polymerization initiator comprising at least two photo-initiators in a predetermined ratio that generate a highly reactive species when irradiated with radiation. The principal resin may comprise a hyperbranched polyester acrylate oligomer content in a range between 5 percent and 96 percent as a percentage of weight of the composition and PETA content in a range between 0 percent and 70 percent as a percentage of weight of the composition. The free radical-polymerization initiator may comprise initiator content in a range between 1 percent and 5 percent as a percentage of weight of the composition to absorb shorter wavelengths, that has maximum absorption in a range between 200 nanometers and 300 nanometers such as, for example, 1-hydroxycyclohexyl phenyl ketone and initiator content in a range between 0.5 percent and 4 percent as a percentage of weight of the composition to absorb longer wavelengths, that has absorption in a range between 300 nanometers and 420 nanometers, such as, for example, diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide, where for the examples given, the predetermined ration is 4-to-1. In one or more embodiments of the present invention, the predetermined ratio of the first initiator to the second initiator is in a range between 5-to-1 and 2-to-1. A solvent comprising 1-methoxy-2-propanol content in a range between 10 percent and 80 percent as a percentage of weight of the composition. The coating composition was deposited on PMMA and PET substrates followed by UV radiation curing to achieve hard-coat films with a thickness ranging from 5 micrometers to 20 micrometers. The applied hard coat exhibited high pencil hardness (8H to 9H for PMMA substrate and 4H to 6H for PET substrate) with a loading of 750 grams based on ASTM D-3363 test, excellent abrasion resistance with no obvious scratch after 1000 cycles of steel-wool test with a loading of 750 grams based on ASTM F-2357 test, and excellent adhesion of 5B based on ASTM D-3359 test.
In still other embodiments, a radiation-curable hard coat composition may include a principal resin comprising multi-(meth)acrylate functionalized oligomers or polymers and a free radical-polymerization initiator comprising at least two photo-initiators in a predetermined ratio that generate a highly reactive species when irradiated with radiation. The principal resin may comprise aliphatic urethane acrylate content in a range between 5 percent and 90 percent as a percentage of weight of the composition and PETA content in a range between 0 percent and 70 percent as a percentage of weight of the composition. The free radical-polymerization initiator may comprise 1-hydroxycyclohexyl phenyl ketone content and diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide content in a 1-to-1 ratio where each constitutes in a range between 1 percent and 4 percent as a percentage of weight of the composition. In one or more embodiments of the present invention, the predetermined ratio of the first initiator to the second initiator is in a range between 5-to-1 and 2-to-1. A solvent comprising 1-methoxy-2-propanol content in a range between 10 percent and 80 percent as a percentage of weight of the composition. The coating composition was deposited on PMMA and PET substrates followed by UV radiation curing to achieve hard-coat films with a thickness ranging from 5 micrometers to 20 micrometers. The applied hard coat exhibited high pencil hardness (4H to 7H for PMMA substrate and 2H to 4H for PET substrate) with a loading of 750 grams based on ASTM D-3363 test, excellent abrasion resistance with no obvious scratch after 1000 cycles of steel-wool test with a loading of 750 grams based on ASTM F-2357 test, and excellent adhesion of 5B based on ASTM D-3359 test.
Advantages of one or more embodiments of the present invention may include one or more of the following:
In one or more embodiments of the present invention, a radiation-curable hard-coat composition provides a hard-coat that is easy to apply, cures efficiently in a single UV irradiation cycle, provides improved flexibility and hardness, and provides improved process-ability for use in a manufacturing environment.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition provides improved flexibility while maintaining a high degree of hardness and scratch and abrasion resistance.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition reduces fragility and brittleness that reduces or eliminates undesirable breakage, cracking, and other failure modes that occur in post-fabrication processing of substrates with applied coatings.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition reduces curling by lowering the built-in stress that significantly reduces the curling angle when the coating is applied to substrates with low mechanical strength, such as, for example, flexible PET substrates used in touch sensor applications.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition includes a principal resin comprising multi-(meth)acrylate functionalized oligomers or polymers.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition includes a principal resin comprising multi-(meth)acrylate functionalized oligomers or polymers that may be derived from various chemical backbones including, for example, polyol, polyester, polyurethane, polyether, epoxies, and acrylics.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition includes a principal resin comprising multi-(meth)acrylate functionalized oligomers or polymers that may be linear or branched. Because of the skeleton of the resin backbone and the molecular geometry, these multi-(meth)acrylate functionalized oligomers or polymers are highly viscous in the liquid state.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition includes a principal resin comprising multi-(meth)acrylate functionalized oligomers or polymers that, after curing, form a hard and rigid polymer with high tensile strength and modulus.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition includes a principal resin comprising multi-(meth)acrylate functionalized oligomers or polymers that, after curing, exhibit a comparatively small shrinkage in volume that induces a low level of built-in stress and reduces the curling angle of the applied coating.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition includes a multi-constituent photo-initiator comprised of at least two different photo-initiators.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition includes a multi-constituent photo-initiator comprised of one or more surface curing agents and one or more deep curing agents that improve curing efficiency and provide homogenous curing along the depth of the applied coating
In one or more embodiments of the present invention, a radiation-curable hard-coat composition includes a multi-constituent photo-initiator that provides substantial absorption in a range between 200 nanometer and 480 nanometers.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition includes a multi-constituent photo-initiator that minimizes spectral interference.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition includes a multi-constituent photo-initiator that provides a high degree of photo-initiation efficiency in a single irradiation cycle.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition includes a multi-constituent photo-initiator that allows for a high coating speed of up to 200 feet per minute in a high volume manufacturing environment with low defects, high yield, and excellent coating performance.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition includes a solvent or co-solvents that prevent aggregation of the multi-(meth)acrylate functionalized oligomers or polymers in the micro scale.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition includes a solvent or co-solvents that reduces or eliminates air bubbles that quench free radicals and reduce the optical performance of the coating.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition provides improved optical performance including high transmission yield and low haze.
In one or more embodiments of the present invention, a radiation-curable hard-coat composition may be effectively applied using spray coating, slot-die coating, dip-coating, and reverse-gravure coating techniques.
While the present invention has been described with respect to the above-noted embodiments, those skilled in the art, having the benefit of this disclosure, will recognize that other embodiments may be devised that are within the scope of the invention as disclosed herein. Accordingly, the scope of the invention should be limited only by the appended claims.
This application is a continuation-in-part of U.S. patent application Ser. No. 14/354,507, filed on Aug. 5, 2014, which is a national phase entry of PCT International Application PCT/US2012/042050, filed on Jun. 12, 2012, which claims the benefit of, or priority to, U.S. Provisional Patent Application Ser. No. 61/551,009, filed on Oct. 25, 2011, and is also a continuation-in-part of U.S. patent application Ser. No. 14/354,526, filed on Apr. 25, 2014, which is a national phase entry of PCT International Application PCT/US2012/061602, filed on Oct. 24, 2012, which claims the benefit of, or priority to, U.S. Provisional Patent Application Ser. No. 61/551,030, filed on Oct. 25, 2011, all of which are hereby incorporated by reference in their entirety.
| Number | Date | Country | |
|---|---|---|---|
| 61551009 | Oct 2011 | US | |
| 61551030 | Oct 2011 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 14354507 | Aug 2014 | US |
| Child | 14727789 | US | |
| Parent | 14354526 | Apr 2014 | US |
| Child | 14354507 | US |
