Patent Application
20190338141
A variety of coatings and films are used to protect windows (e.g., building and automobile windows) and optical displays (e.g., as cathode ray tube (CRT) and light emitting diode (LED) displays).
Additional options for protecting windows and optical displays are desired, particularly those having relatively good or better hardness, weatherability, and optical properties (e.g., visibility) at the same time.
In one aspect, the present disclosure provides an article comprising, in order:
a substrate;
a hardcoat comprising:
a layer comprising SiOxCy, where 0<x<2 and 0<y<1; and
a hydrophilic layer.
Embodiments of articles described herein typically have good transparency and hardness, and are useful, for example, for optical displays (e.g., cathode ray tubes (CRT) and light emitting diode (LED) displays), personal digital assistants (PDAs), cell phones, liquid crystal display (LCD) panels, touch-sensitive screens, removable computer screens, window films, and goggles.
The FIGURE is a schematic of a side view of an exemplary article described herein.
Referring to the FIGURE, article 100 comprising, in order, substrate 102, hardcoat 104, layer 108, and hydrophilic layer 109. Hardcoat 104 comprises binder 105 and nanoparticles 106. Layer 108 comprises SiOxCy, where 0<x<2 and 0<y<1.
Substrates
Exemplary substrates for having the hardcoat described herein thereon include a film, a polymer plate, a sheet glass, and a metal sheet. The film may be transparent or non-transparent. As used herein “transparent” refers that total transmittance is 90% or more and “untransparent” refers that total transmittance is less than 90%. Exemplary films includes those made of polycarbonate, poly(meth)acrylate (e.g., polymethyl methacrylate (PMMA)), polyolefins (e.g., polypropylene (PP)), polyurethane, polyesters (e.g., polyethylene terephthalate (PET)), polyamides, polyimides, phenolic resins, cellulose diacetate, cellulose triacetate, polystyrene, styrene-acrylonitrile copolymers, acrylonitrile butadiene styrene copolymer (ABS), epoxies, polyethylene, polyacetate and vinyl chloride, or glass. The polymer plate may be transparent or non-transparent. Exemplary polymer plates include those made of polycarbonate (PC), polymethyl methacrylate (PMMA), styrene-acrylonitrile copolymers, acrylonitrile butadiene styrene copolymer (ABS), a blend of PC and PMMA, or a laminate of PC and PMMA. The metal sheet may be flexible or rigid. As used herein, “flexible metal sheet” refers to metal sheets that can undergo mechanical stresses (e.g., bending or stretching) without significant irreversible change. “Rigid metal sheet” refers to metal sheets that cannot undergo mechanical stresses (e.g., bending or stretching) without significant irreversible change. Exemplary flexible metal sheets include those made of aluminum. Exemplary rigid metal sheets include those made of aluminum, nickel, nickel-chrome, and stainless steel. When metal sheets are used, it may be desirable to apply a primer layer between the hardcoat and the substrate.
Typically, the thickness of the film substrate is in a range from about 5 micrometers to about 500 micrometers. Typically the thickness for a polymer plate is in a range from about 0.5 mm to about 10 mm (in some embodiments, from about 0.5 mm to about 5 mm, or even about 0.5 mm to about 3 mm). For sheet glass or metal sheet as the substrate, the typical thickness is in a range from about 5 micrometers to about 500 micrometers (in some embodiments, about 0.5 mm to about 10 mm, about 0.5 mm to about 5 mm, or even about 0.5 mm to about 3 mm). Thickness outside of these ranges may also be useful.
Optional Primer
In some embodiments, the substrate includes a primer such that a primer layer is between the substrate and the hardcoat layer. Substrates having a primer layer thereon are commercially available. For example, a primed polyethylene terephthalate (PET) substrate is available under trade designation “LUMIRROR U32” from Toray Industries, Inc., Tokyo, Japan; and “COSMOSHINE” from Toyobo Co., Ltd., Tokyo, Japan.
Techniques for applying the primer precursor (solution) to the surface of the substrate are known in the art, and include bar coating, dip coating, spin coating, capillary coating, spray coating, gravure coating, and screen printing. The coated primer precursor can be dried and cured by polymerization methods known in the art such as ultraviolet (UV) or thermal polymerization.
Binder
The amount of binder in the precursor to form the hardcoat is typically sufficient to provide the hardcoat with binder present in a range from 10 wt. % to 40 wt. %, based on the total weight of the hardcoat.
Exemplary binders include at least one of cured (meth)acrylic oligomer or monomer.
Exemplary binders such as trifunctional aliphatic urethane acrylate are available, for example, from Daicel-Allnex, Ltd., under the trade designation “EBECRYL 8701.”
In some embodiments, the binder (and hardcoat) comprise at least one silicone (meth)acrylate additive (e.g., polydimethylsiloxane (PDMS) having at least one of an acrylate, (meth)acrylate, hydroxyl, glycidyl, carbonyl, amino, or (m)ethoxy group). For example, the silicone (meth)acrylate additive is present in an amount in a range from 0.01 wt. % to 10 wt. %, based on the total weight of the hardcoat layer.
Nanoparticles
Exemplary nanoparticles include at least one of SiO2 nanoparticles, ZnO nanoparticles, ZrO2 nanoparticles, indium-tin-oxide (ITO) nanoparticle or antimony-doped tin oxide (ATO) nanoparticles. Suitable nanoparticles are known in the art and include SiO2, which is available, for example, under trade designation “NALCO 2327” from Nalco Company, Naperville, Ill.; and ZnO, which is available, for example, under trade designation“NANOBYK3820” from BYK Japan KK, Tokyo, Japan; ZrO2, which is available, for example, under the trade designation “BAILAR Zr—C20” from Taki Chemical, Ltd., Hyogo, Japan; indium-tin oxide, which is available, for example, under the trade designation “PI-3;” from Mitsubishi Materials Electronic Chemicals Co., Ltd., Akita, Japan; and antimony doped tin oxide, which is available, for example, under the trade designation “549541” from Sigma-Aldrich Co. LLC, St. Louis, Mo.
In general, the nanoparticles themselves (i.e., absent any coating) have a particle size in a range from about 2 nm to 400 nm (in some embodiments, 2 nm to 300 nm). The average diameter of nanoparticles is measured with transmission electron microscopy (TEM) using commonly employed techniques in the art. For measuring the average particle size of nanoparticles, sol samples can be prepared for TEM imaging by placing a drop of the sol sample onto a 400 mesh copper TEM grid with an ultra-thin carbon substrate on top of a mesh of lacey carbon (available from Ted Pella Inc., Redding, Calif.). Part of the drop can be removed by touching the side or bottom of the grid with filter paper. The remainder can be allowed to dry. This allows the particles to rest on the ultra-thin carbon substrate and be imaged with less interference from a substrate. TEM images can be recorded at multiple locations across the grid. Enough images are recorded to allow sizing of 500 to 1000 particles. The average diameters of the nanoparticles can then be calculated based on the particle size measurements for each sample. TEM images can be obtained using a high resolution transmission electron microscope (available under the trade designation “HITACHI H-9000” from Hitachi, Tokyo, Japan) operating at 300 KV (with a LaB6 source). Images can be recorded using a camera (e.g., Model No. 895, 2 k×2 k chip available under the trade designation “GATAN ULTRASCAN CCD” from Gatan, Inc., Pleasanton, Calif.). Images can be taken, for example, at a magnification of 50,000× and 100,000×. For some samples, images may be taken at a magnification of 300,000×.
Hardcoat Layer
A hardcoat precursor can be prepared by combining components using techniques known in the art, such as adding curable monomers and/or oligomers in solvent (e.g., methyl ethyl ketone (MEK) or 1-methoxy-2-propanol (MP-OH)) with an inhibitor to solvent. In some embodiments, depending, for example, on the curable monomers and/or oligomers used, a solvent-free (i.e., organic solvent free, or 100% water) process may be used to form the coatings.
In some embodiments, two or more different sized nanoparticle sols, with or without modification, may be mixed with curable monomers and/or oligomers in solvent with an initiator to furnish a hardcoat precursor. The desired weight % in solid of the hardcoat precursor can be adjusted by adding the solvent.
Optionally, the hardcoat may further include known additives such as an anti-fog agent, an antistatic agent, and an easy clean agent (e.g., an anti-fingerprinting agent, an anti-oil agent, an anti-lint agent, an anti-smudge agent, or other agents adding an easy-cleaning function).
Inclusion of silicon polyether acrylate (available, for example, under the trade designation “TEGORAD 2250” from Evonic Goldschmidt GmbH, Essen, Germany) in the hardcoat may also improve the easy-clean function of the hardcoat. Exemplary amounts of silicon polyether acrylate include in a range from about 0.01 wt. % to about 5.0 wt. % (in some embodiments, about 0.05 wt. % to about 1.5 wt. %, or even about 0.1 wt. % to about 0.5 wt. %), based on the total weight of the hardcoat.
Techniques for applying the hardcoat precursor (solution) to the surface of the substrate are known in the art, and include bar coating, dip coating, spin coating, capillary coating, spray coating, gravure coating, and screen printing. The coated hardcoat precursor can be dried and cured by polymerization methods known in the art such as ultraviolet (UV) or thermal polymerization.
For those substrates having more than one surface, a hardcoat may be disposed on more than one surface of the substrate. Also, more than one hardcoat layer may be applied to a surface.
Typically, the hardcoat layer has a thickness up to 100 micrometers (in some embodiments, up to 50 micrometers, or even up to 10 micrometers; in some embodiments, in a range from 1 micrometer to 50 micrometers, or even 1 micrometer to 10 micrometers).
SiOxCy Layer
The layer comprising SiOxCy can be provided, for example, via plasma-enhanced chemical vapor deposition (PECVD), wherein the plasma is formed, for example, from 1,1,3,3-tetramethyldisiloxane (TMDSO) and oxygen gas, or hexamethyledisiloxane (HMDSO) and oxygen gas.
The plasma density is the calculated power (e.g., RF (13.56 MHz) applied per unit area of the electrode). In some embodiments, plasma density is greater than 0.1 W/cm2 (in some embodiments, greater than 0.2 W/cm2 or even 0.23 W/cm2).
Plasma dose is the plasma density per resident time. In some embodiment, the plasma dose range is in a range from 1 Joule/cm2 to 15 Joule/cm2 (in some embodiments, 4 Joule/cm2 to 10 Joule/cm2).
In some embodiments, the layer comprising SiOxCy has a thickness up to 5 micrometers (in some embodiments, in a range 5 nm to 5 micrometer; 10 nm to 500 nm, 25 nm to 500 nm, 25 nm to 250 nm, or even 50 nm to 150 nm).
In some embodiments, the layer comprising SiOxCy is amorphous. In some embodiments, the layer comprising SiOxCy is hydrophilic. The degree of hydrophilicity is observed to change based on the ratio of Si:O:C. In some embodiments, the layer comprising SiOxCy has a water contact angle not greater than 40 degrees (in some embodiments, not greater than 35 degrees, 30 degrees, 25 degrees, or even 20 degrees) as measured by the “Water Contact Angle Determination” in the Examples.
In some embodiments, the layer comprising SiOxCy has a haze value less than 3% as determined by the “Haze Test” described in the Examples. In some embodiments, the layer comprising SiOxCy has a haze value less than 0.2% as determined by the “Haze Test” described in the Examples.
Hydrophilic Layer
Exemplary materials for preparing a hydrophilic composition for providing the hydrophilic layer include at least one of alcoxy silane or zwitter ionic alcoxy silane in water. Hydrophilic materials are commercially available, for example, under the trade designation “LAMBIC 400EP” from Osaka Organic Chemical Industry, Ltd., Osaka, Japan. In some embodiments the hydrophilic material (e.g., alcoxy silane) is present in a range from 0.001 wt. % to 40 wt. % (in some embodiments, in a range from 0.001 wt. % to 30 wt. %, 0.001 wt. % to 20 wt. %, 0.001 wt. % to 10 wt. %, 0.5 wt. % to 5 wt. %, or even 1 wt. % to 4 wt. %), based on the total weight of the hydrophilic composition. In some embodiments, the hydrophilic layer comprises a silane coupling agent having at least one of zwitterionic or polyethylene glycol (PEG) functionality.
Techniques for applying the hydrophilic composition to the surface of the layer comprising SiOxCy are known in the art, and include bar coating, dip coating, spin coating, capillary coating, spray coating, gravure coating, and screen printing. The coated hydrophilic composition can be dried and cured with hydrolysis and condensation reaction.
In some embodiments, the hydrophilic layer has a thickness up to 1 micrometer (in some embodiments, in a range from 5 nm to 1 micrometer, 5 nm to 500 nm, 5 nm to 100 nm, or even 5 nm to 20 nm).
In some embodiments, the hydrophilic layer has an outer surface, and the outer surface has a haze in range from −1.0 to 1.0 as determined by the “Haze Test” described in the Examples.
In some embodiments, the hydrophilic layer has an outer surface, wherein the outer surface has an “OK” of easy clean performance as determined by the “Easy Clean Test” described in the Examples.
In some embodiments, the hydrophilic layer has an outer surface, wherein the outer surface has an “OK” for anti-fogging performance as determined by the “Anti-Fogging Test” described in the Examples.
Optional Adhesive Layer
Optionally, an adhesive layer may be applied on the opposite surface of the substrate having the hardcoat layer thereon. Exemplary adhesives are known in the art, and include acrylic adhesive, urethane adhesive, silicone adhesive, polyester adhesive, and rubber adhesive.
Further, if an adhesive layer is present, optionally a liner (e.g., release liner) is included over the adhesive layer. Release liners are known in the art and include paper and a polymer sheet.
Articles described herein are useful, for example, for optical displays (e.g., cathode ray tube (CRT), light emitting diode (LED) displays), plastic cards, lenses, camera bodies, fans, door knobs, tap handles, mirrors, and home electronics (e.g., washing machines), and for optical displays (e.g., cathode ray tube (CRT) and light emitting diode (LED) displays), personal digital assistants (PDAs), cell phones, liquid crystal display (LCD) panels, touch-sensitive screens, removable computer screens, window films, and goggles. Further, the hardcoat described herein may be useful, for example, for furniture, doors and windows, toilet bowls and bath tubs, vehicle interiors/exteriors, camera lenses and glasses, and solar panels.
1A. An article comprising, in order:
a substrate;
a hardcoat comprising:
a layer comprising SiOxCy, where 0<x<2 and 0<y<1; and
a hydrophilic layer.
2A. The article of Exemplary Embodiment 1A, wherein the substrate comprises one of a film, a polymer plate, a glasssheet, and a metal sheet.
3A. The article of any preceding A Exemplary Embodiment, further comprising a primer layer between the substrate and the hardcoat layer.
4A. The article of any preceding A Exemplary Embodiment, wherein the binder comprises at least one of cured (meth)acrylic oligomer or monomer.
5A. The article of any preceding A Exemplary Embodiment, wherein the binder is present in a range from 5 wt. % to 60 wt. %, based on the total weight of the hardcoat.
6A. The article of any preceding A Exemplary Embodiment, wherein the hardcoat comprises at least one silicone (meth)acrylate additive (e.g., polydimethylsiloxane (PDMS) acrylate).
7A. The article of Exemplary Embodiment 6A, wherein the at least one silicone (meth)acrylate additive is present in an amount in a range from 0.01 wt. % to 10 wt. %, based on the total weight of the hardcoat layer.
8A. The article of any preceding A Exemplary Embodiment, wherein the nanoparticles are at least one of SiO2 nanoparticles, ZnO nanoparticles, ZrO2 nanoparticles, indium-tin-oxide (ITO) nanoparticles or antimony-doped tin oxide (ATO) nanoparticles.
9A. The article of any preceding A Exemplary Embodiment, wherein the hardcoat layer has a thickness up to 100 micrometers (in some embodiments, up to 50 micrometers, or even up to 10 micrometers; in some embodiments, in a range from 1 micrometer to 50 micrometers, or even 1 micrometer to 10 micrometers).
10A. The article of any preceding A Exemplary Embodiment, wherein the layer comprising SiOxCy is amorphous.
11A. The article of any preceding A Exemplary Embodiment, wherein the layer comprising SiOxCy is hydrophilic.
12A. The article of any preceding A Exemplary Embodiment, wherein the layer comprising SiOxCy has a water contact angle not greater than 40 degrees (in some embodiments, not greater than 35 degrees, 30 degrees, 25 degrees, even 20 degrees) as determined by the Water Contract Angle Determination described in the Examples.
13A. The article of any preceding A Exemplary Embodiment, wherein the layer comprising SiOxCy has a haze value less than 3% as determined by the Haze Test described in the Examples.
14A. The article of Exemplary Embodiment 13A, wherein the layer comprising SiOxCy has a haze value less than 0.2% as determined by the Haze Test described in the Examples.
15A. The article of any preceding A Exemplary Embodiment, wherein the hydrophilic layer has an outer surface, and wherein said outer surface has a haze in range from −1.0 to 1.0 as determined by the Haze Test described in the Examples.
16A. The article of any preceding A Exemplary Embodiment, wherein the layer comprising SiOxCy has a thickness up to 5 micrometers (in some embodiments, in a range 5 nm to 5 micrometers, 10 nm to 500 nm, 25 nm to 500 nm, 25 nm to 250 nm, or even 50 nm to 150 nm).
17A. The article of any preceding A Exemplary Embodiment, wherein the hydrophilic layer comprises a silane coupling agent having at least one of zwitterionic or polyethylene glycol (PEG) functionality.
18A. The article of any preceding A Exemplary Embodiment, wherein the hydrophilic layer has a thickness up to 1 micrometer (in some embodiments, in a range from 5 nm to 1 micrometer, 5 nm to 500 nm, 5 nm to 100 nm, or even 5 nm to 20 nm).
19A. The article of any preceding A Exemplary Embodiment passing the Easy Clean Test described in the Examples.
20A. The article of any preceding A Exemplary Embodiment passing the Anti-Fogging Test described in the Examples.
1B. A method of making the article of any preceding A Exemplary Embodiment comprising:
providing a substrate with the hardcoat thereon, and in turn, the layer comprising SiOxCy; on the hardcoat; and
applying the hydrophilic layer on the layer comprising SiOxCy.
2B. The method of Exemplary Embodiment 1B, further comprising, providing the layer comprising SiOxCy via plasma-enhanced chemical vapor deposition (PECVD), wherein the plasma is formed from 1,1,3,3-tetramethyldisiloxane (TMDSO) and oxygen gas, or hexamethyledisiloxane (HMDSO) and oxygen gas.
3B. The method of any preceding B Exemplary Embodiment, further comprising, providing the hardcoat layer via:
depositing a layer comprising uncured binder and a mixture of nanoparticles in a range from 60 wt. % to 90 wt. %, based on the total weight of the hardcoat, wherein a range from 10 wt. % to 50 wt. % (in some embodiments, in a range from 15 wt. % to 45 wt. %, or even from 20 wt. % to 40 wt. %) of the nanoparticles comprise a first group of nanoparticles having an average particle diameter in a range from 2 nm to 200 nm (in some embodiments, in a range from 2 nm to 150 nm), and in a range from 50 wt. % to about 90 wt. % (in some embodiments, in a range from 55 wt. % to 85 wt. %, or even from 60 wt. % to 80 wt. %) of the nanoparticles comprise a second group of nanoparticles having an average particle diameter in a range from 60 nm to 400 nm (in some embodiments, in a range from 70 nm to 300 nm), based on the total weight of nanoparticles in the hardcoat, and having a ratio of the average particle size of the first group of nanoparticles to the average particle size of the second group of nanoparticles are in a range from 1:2 to 1:200 (in some embodiments, 1:2.5 to 1:100); and
curing the binder.
4B. The method of Exemplary Embodiment 3B, wherein the uncured binder comprises at least one silicone (meth)acrylate additive (e.g., polydimethylsiloxane (PDMS) acrylate).
5B. The method of Exemplary Embodiment 4B, wherein the at least one silicone (meth)acrylate additive is present in an amount in a range from 0.01 wt. % to 10 wt. %, based on the total weight of the hardcoat layer.
6B. The method of any of Exemplary Embodiments 3B to 5B, further comprising, providing the hydrophilic layer via depositing a hydrophilic composition comprising alcoxy silane.
7B. The method of Exemplary Embodiment 6B, wherein the alcoxy silane is present in a range from 0.001 wt. % to 40 wt. % (in some embodiments, in a range from 0.001 wt. % to 30 wt. %, 0.001 wt. % to 20 wt. %, 0.001 wt. % to 10 wt. %, 0.5 wt. % to 5 wt. %, or even 1 wt. % to 4 wt. %), based on the total weight of the hydrophilic composition.
8B. The method of either Exemplary Embodiment 6B or 7B, wherein the hydrophilic composition further comprises at least one of water or an alcohol (e.g., ethanol).
9B. The method of Exemplary Embodiments 6B to 8B, wherein the composition further comprises a silane coupling agent having at least one of zwitterionic or polyethylene glycol (PEG) functionality.
Advantages and embodiments of this invention are further illustrated by the following examples, but the particular materials and amounts thereof recited in these examples, as well as other conditions and details, should not be construed to unduly limit this invention. Unless otherwise noted, all parts, percentages, ratios, etc., in the Examples and the rest of the specification are by weight.
The pencil hardness of the samples prepared according to the Examples and Comparative Examples was determined according to JIS K 5600-5-4 (1999), the disclosure of which is incorporated herein by reference. The test was run by rubbing the samples with pencil leads of varying hardnesses (from softest to hardest) at a 45-degree angle under an applied load of 750 grams and determining the highest pencil hardness a sample survived, without scratching. The pencil hardness tester used for this method was obtained under trade designation “NO. 431 PENCIL SCRATCH HARDNESS TESTER” from Toyo Seiki Seisaku-Sho, Ltd., Tokyo, Japan.
Adhesion performance of the samples prepared according to the Examples and Comparative Examples was evaluated by a cross-cut test according to JIS K5600-5-6 (1999), the disclosure of which is incorporated herein by reference. Adhesion test assesses the resistance of a coating to separation from the substrate. First, a right angle lattice pattern (a 5×5 grid with 1 mm of interval grid (i.e., 25 one mm by one mm squares)) was cut into the coating penetrating through to the substrate. An adhesive tape (obtained under the trade designation “NICHIBAN CT24” from Nitto Denko Co., Ltd., Osaka, Japan) was adhered over the lattice and then pulled off at a right angle. Presence/absence of cracks on the lattice was then determined by using an optical microscope. A lack of cracking (or presence of only a few cracks), is an indication of more desirable or improved flexibility and adherence. The results are reported as the number of squares lacking cracks out of the 25 cut in the sample and a tape.
The optical properties such as clarity, haze, and percent transmittance (TT) of the samples prepared according to the Examples and Comparative Examples were measured by using a haze meter (obtained under the trade designation “NDH5000W” from Nippon Denshoku Industries Co., Ltd, Tokyo, Japan). Optical properties were determined on as-prepared samples (i.e., initial optical properties) and after subjecting the samples to steel wool abrasion resistance testing. The “Haze Test” compared the difference in haze values before and after subjecting the samples to steel wool abrasion resistance testing.
The scratch resistance of the samples, prepared according to the Examples and Comparative Examples, was evaluated by the surface changes after the steel wool abrasion test using 2.7×2.7 cm2 head area with #0000 steel wool after 20 cycles at 500 grams load and at 60 cycles/min. rate. The strokes were 85 mm long. The instrument used for the test was an abrasion tester (obtained under the trade designation “IMC-157C” from Imoto Machinery Co., Ltd., Kyoto Japan). The optical properties (percent transmittance, haze, and Haze (i.e., haze after abrasion test minus initial haze)) were measured again using the method described above.
The presence of scratches was rated as described in Table 1, below.
The water contact angle of a surface of the samples, prepared according to the Examples and Comparative Examples, was measured by sessile drop method using a contact angle meter (obtained under the trade designation “DROPMASTER FACE” from Kyowa Interface Science Co., Ltd., Saitama, Japan). The contact angle was measured from an optical photograph image after 2.0 microliters of water were dropped on the surface. The value of contact angle was calculated from the average of 5 measurements.
The easy clean performance of the samples, prepared according to the Examples and Comparative Examples, was evaluated by removing or attempting to remove an ink mark (made from a marker obtained under the trade designation “MACKEE EXTRA FINE MO-120-MC-BK” from Zebra, Co., Ltd., Tokyo, Japan) using a wet cotton ball. The wet cotton ball was swiped back and forth, up to five times, over the ink mark under moderate manual force. The easy clean performance of the samples was then determined by visual inspection and rated based on the following criteria:
The anti-fogging performance of the samples, prepared according to the Examples and Comparative Examples, was evaluated by the visual inspection as follows. 450 mL of water was added into 500 mL conical flask. The temperature of the water was controlled to 60° C. The sample tested was held 10 cm above the water level in the flask. Then, the time until fogging up of the sample was observed.
The anti-fogging performance was rated with the following criteria:
5.95 grams of 3-methacryloxypropyl-trimethoxysilane (obtained under trade designation “SILQUEST A-174” from Alfa Aesar, Ward Hill, Mass.,) and 0.5 gram of 4-hydroxy-2,2,6,6-tetramethylpiperidine 1-oxyl (5 wt. %; obtained under trade designation “PROSTAB” from Aldrich Chemical Company, Milwaukee, Wis.) was added to a mixture of 400 grams of 75 nm diameter SiO2 sol (obtained under trade designation “NALCO 2329” from Nalco Company, Naperville, Ill.) and 450 grams of 1-methoxy-2-propanol (obtained from Sigma-Aldrich Co., LLC, St. Louis, Mo.) in a glass jar with stirring at room temperature for 10 minutes. The jar was sealed and placed in an oven at 80° C. for 16 hours. The water was removed from the resultant solution with a rotary evaporator at 60° C. until the solid content of the solution was about 45 wt. %. 200 grams of 1-methoxy-2-propanol was charged into the resultant solution, and the remaining water removed using the rotary evaporator at 60° C. This latter step was repeated for a second time to further remove water from the solution. Sufficient amount of 1-methoxy-2-propanol was added to the sol to provide a SiO2 sol containing 45.0 wt. % of surface modified SiO2 nanoparticles with an average size of 75 nm (“Sol-1”).
25.25 grams of 3-methacryloxypropyl-trimethoxysilane (“SILQUEST A-174”) and 0.5 gram of 4-hydroxy-2,2,6,6-tetramethylpiperidine 1-oxyl (5 wt. %; “PROSTAB”) was added to a mixture of 400 grams of 20 nm diameter SiO2 sol (obtained under trade designation “NALCO 2327” from Nalco Company) and 450 grams of 1-methoxy-2-propanol in a glass jar with stirring at room temperature for 10 minutes. The jar was sealed and placed in an oven at 80° C. for 16 hours. The water was removed from the resultant solution with a rotary evaporator at 60° C. until the solid content of the solution was about 45 wt %. 200 grams of 1-methoxy-2-propanol was charged into the resultant solution, and the remaining water removed by using the rotary evaporator at 60° C. This latter step was repeated for a second time to further remove water from the solution. Sufficient amount of 1-methoxy-2-propanol was added to the sol to provide a SiO2 sol containing 45.0 wt. % of surface modified SiO2 nanoparticles with an average size of 20 nm (“Sol-2”).
42.98 grams of Sol-1, 23.14 grams of Sol-2, 8.93 grams of trifunctional aliphatic urethane acrylate (obtained from under trade designation “EBECRYL 8701” from Daicel-Allnex, Ltd. Tokyo, Japan) and 0.99 gram of 1,6-hexanediol diacrylate (obtained under trade designation “SARTOMER SR238NS” from Arkema Americas, Clear Lake, Tex.) were mixed. 0.79 gram of 1-[4-(2-hydroxyethoxy)-phenyl]-2-hydroxy-2-methyl-1-propane-1-one (obtained under trade designation “IRGACURE 2959” from BASF Japan Ltd., Tokyo, Japan) as the photoinitiator and 0.02 gram of acrylated poly dimethyl siloxane (PDMS) (obtained under trade designation “TEGORAD 2250” from Evonik Industries, Essen, Germany) was added to the mixture. The mixture was adjusted to 40.49 wt. % in solid by adding 19.84 grams of metylisobutyl ketone (obtained from obtained from Sigma-Aldrich Co., LLC) and 3.31 grams of 1-methoxy-2-propanol (obtained from Sigma-Aldrich Co., LLC) to prepare the hardcoat precursor solution (“HC-1”).
A 100-micrometer thick polyethylene terephthalate (PET) film (obtained under trade designation“LUMIRROR U34” from Toray Industries, Inc., Tokyo, Japan) was used as a substrate. HC-1 hardcoat precursor solution was roll-to-roll (R2R) coated onto the PET film using gravure coating line equipped with a 2-inch (5 cm) diameter gravure coating roll. The gravure coating roll had 130 grooves per lineal inch (51 grooves per lineal cm) and was operated at a wiping ratio of 180%. The HC-1 hardcoat precursor solution (40.49 wt. % solids) was filtered in-line using a filter (obtained under the trade designation “HT-40EY ROKI” from Roki Techno Co., Ltd., Tokyo, Japan). The coating was first cured by passing the sample through an oven equipped with three heating zones. The temperature of the three heating zones (zones 1, 2, and 3) of the oven were set to 87° C., 85° C., and 88° C., respectively. Note that the actual measured temperatures for heating zones 1, 2 and 3 inside the oven were 59° C., 67° C., and 66° C., respectively. Each of the heating zones (zones 1, 2 and 3) of the oven was fitted with a fan. The fans for zones 1, 2 and 3 were set to operate at 30 Hz, 40 HZ, and 40 Hz, respectively. Then the coating was ultraviolet (UV) cured under N2 atmosphere (N2 gas having an O2 content of 120-240 ppm) using a Fusion UV curing system equipped with an H-bulb (240 W/cm power; obtained under trade designation “HERAEUS/FUSION UV F600 SERIES” from Heraeus Noblelight America, LLC, Buford, Ga.). Line speed through the UV curing system was fixed at 6 meters per minute and the UV power was set at 40% output. The web tension was 20, 24, 19 and 20 N (for a 250-mm web) at unwinder, input, oven, winder, respectively. For the unwinder and winder, 3-inch (7.5 cm) diameter roll cores were used.
A (R2R) plasma deposition system was used for deposition of SiOx on the coated polymer films. The system included an aluminum vacuum chamber that contained two roll shape electrodes with chamber walls acting as the counter electrode. Because of the larger surface area of the counter electrode, the system was considered to be asymmetric, resulting in large sheath potential at the powered electrode, around which the substrate film to be coated was wrapped. The chamber was pumped by pumping system, which included dual turbo-molecular pumps backed by a mechanical pump. Process gases were metered through mass flow controllers and blended in a manifold before they were introduced into the chamber. The process gases, oxygen, and hexamethyldisiloxane (obtained under the trade designation “HMDSO” from Iwatani Corporation, Tokyo, Japan) were stored remotely in gas cabinets and piped to the mass flow controller. The plasma was powered by a 13.56 MHz-10500W radio frequency power supply (obtained under the trade designation “MKS SPECTRUM” (Model B-10513) from MKS Instruments, Inc., Andover, Mass.) through an impedance matching network (Model MWH-100, obtained from MKS Instruments, Inc.). The hard coated substrate described above was treated by R2R plasma equipment using one of the conditions described in Table 2, below. The mixed gases of hexamethyldisiloxane (“HMDSO”) and oxygen provided the resulting SiOx layer on the hardcoat layer.
EX-1 was prepared as follows. HC-1 was coated on a 100-micrometer thick PET film (“LUMIRROR U34”) and cured as described above (see “Coating and Curing of Hardcoat Layer”), resulting in a PET film having a 3-micrometer thick (dry) nanoparticle-filled hardcoat. The hardcoated substrate was treated by using the R2R plasma equipment (see “Plasma Deposition”) with process condition #2, in Table 2 (above).
The plasma deposited film was fixed on a soda lime glass plate with a size of 50 mm×150 mm×3 mm. 5 wt. % of a hydrophilic silane (obtained under trade designation “LAMBIC 400EP” from Osaka Organic Chemical Industry, Ltd., Osaka, Japan) was applied as a hydrophilic topcoat by applied on to the plasma-deposited hardcoat film substrate. The hydrophilic topcoat was coated using a Mayer Rod #4, and dried for 10 minutes at 100° C. in air.
EX-2 was prepared as described for EX-1, except plasma condition #3, in Table 2 (above), was used.
EX-3 was prepared as described for EX-1, except plasma condition #4, in Table 2 (above), was used.
CE-1 was a bare 100-micrometer thick PET film (“LUMIRROR U34”).
CE-2 was prepared as follows. A 100-micrometer thick PET film (“LUMIRROR U34”) was treated with the R2R plasma equipment using the plasma condition #1, in Table 2 (above). No nanoparticle-filled hardcoat was applied. Finally, a hydrophilic silane layer (“LAMBIC 400EP”) was deposited and dried as described above (see EX-1).
The resulting CE-1, CE-2, and EX-1 to EX-3 samples were tested using methods described above. The results are summarized in Table 3, below.
Haze
Foreseeable modifications and alterations of this disclosure will be apparent to those skilled in the art without departing from the scope and spirit of this invention. This invention should not be restricted to the embodiments that are set forth in this application for illustrative purposes.
This application claims the benefit of U.S. Provisional Patent Application No. 62/436,032, filed Dec. 19, 2016, the disclosure of which is incorporated by reference herein in its entirety.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2017/065731 | 12/12/2017 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62436032 | Dec 2016 | US |
