DECORATIVE STRUCTURE
20220287421 · 2022-09-15
Inventors
- Christian TEISSL (Innsbruck, AT)
- Christof Neuhauser (Innsbruck, AT)
- Guenther Blasbichler (Innsbruck, AT)
- Markus Sauer (Mils, AT)
Cpc classification
B44F1/02
PERFORMING OPERATIONS; TRANSPORTING
International classification
B44C1/24
PERFORMING OPERATIONS; TRANSPORTING
Abstract
A decorative structure (20) comprising a planar support (22) and a faceted microstructure (24) on at least one side of the planar support (22) is provided. The decorative structure (20) may further comprise an at least partially reflective layer (26) configured to at least partially reflect light that passes through the microstructure (24). The faceted microstructure (24) comprises a plurality of grooves (28) creating a pattern of facets (30) over the surface of the support (22), such that the microstructure (24) is capable of splitting incident light into spectral colours. In embodiments, the grooves (28) have a triangular or V-shaped profile. Methods of making a decorative structure(20) and articles incorporating the decorative structure (20) are also described.
Claims
1. A decorative structure comprising: a support having a first planar major surface and a second planar major surface opposite the first planar major surface, a microstructure on the first planar major surface of the support, wherein the microstructure comprises a plurality of grooves creating a pattern of facets, and wherein the pattern of facets comprises at least two different types of facets, wherein each different type of facet differs from each other type of facet by its geometry and/or the angle of the facet plane relative to the planar major surface of the support.
2. The decorative structure of claim 1, wherein the decorative structure comprises: an at least partially reflective layer configured to at least partially reflect light that is incident on or passes through the surface of the facets; and two or more superimposed microstructures.
3. The decorative structure of claim 2, wherein the at least partially reflective layer is a reflective or semi-transparent layer that comprises a layer of metal.
4. The decorative structure of claim 1, wherein the grooves have a depth of between 30 μm and 3,000 μm, preferably between 30 μm and 1,000 μm, between 30 μm and 500 μm, or between 30 μm 200 μm.
5. The decorative structure of claim 1, wherein the grooves comprise two planar walls, and the angle between each of the planar walls of the grooves and the planar surface of the support are individually selected from between 5 and 35°.
6. The decorative structure of claim 1, wherein the facets of the microstructure are planar surfaces with low surface roughness and a high degree of flatness.
7. The decorative structure of claim 1, wherein the plurality of grooves comprises a first set of parallel grooves and a second set of parallel grooves that at least partially intersects with the first set of parallel grooves.
8. The decorative structure of claim 7, wherein the grooves within each set of parallel grooves are each spaced from the adjacent groove in the same set by approximately the same distance.
9. The decorative structure of claim 1, wherein the microstructure is formed from a layer of material applied on the support, and/or wherein the microstructure is formed by imprinting the support or a layer or material applied on the support, such as by imprint lithography, and/or wherein the microstructure is made from a transparent material.
10. The decorative structure of claim 1, wherein the support is made from a transparent material and/or wherein the support is a substantially flat structure.
11. The decorative structure of claim 2, wherein the two or more microstructures are separated from each other by the support and/or an at least partially reflective layer.
12. The decorative structure of claim 1, wherein the microstructure is made from a material that is non-diffusive, and/or wherein the microstructure is made from a material that has high optical dispersion; optionally wherein the material has an Abbe number below 60, and/or wherein the microstructure is made from a material obtained by curing a UV curable resin composition, the UV curable resin composition comprising acrylate and/or methacrylate monomers, and having a high aromatic content.
13. A method of making a decorative structure, the method comprising: providing a support having a first planar major surface and a second planar major surface opposite the first planar major surface; and forming a microstructure on the first planar major surface of the support, wherein the microstructure comprises a plurality of grooves creating a pattern of facets, wherein the pattern of facets comprises at least two different types of facets, wherein each different type of facet differs from each other type of facet by its geometry and/or the angle of the facet plane relative to the planar major surface of the support.
14. The method of claim 13, further comprising: (i) forming a second microstructure superimposed over the first microstructure; and (ii) applying an at least partially reflective layer on at least one surface selected from: the first microstructure after it is formed, the second microstructure after it is formed, the first planar major surface of the support prior to forming the first microstructure, and/or the second planar major surface of the support, optionally wherein the second microstructure is formed on the second planar major surface of the support, such that the two microstructures are superimposed and separated from each other by the support and/or an at least partially reflective layer.
15. The method of claim 13, wherein forming a microstructure comprises applying a layer of imprintable material and imprinting a microstructure into the layer of imprintable material using a stamp; optionally wherein the method further comprises curing the imprintable material and/or wherein the method further comprises providing a working stamp by replicating a metallic master stamp into a polymeric stamp material, or by galvanic replication of a metallic master stamp; preferably wherein the working stamp has low surface roughness and high flatness.
16. The method of claim 15, further comprising providing a metallic master stamp, wherein providing a metallic master stamp comprises creating a plurality of substantially triangular grooves in a metal substrate using a monocrystalline diamond cutting tool; optionally wherein the monocrystalline diamond cutting tool has a non-symmetrical triangular shape (cutting profile) and/or wherein creating a plurality of grooves in a metal substrate comprises creating a first set of parallel grooves, a second set of parallel grooves that at least partially intersects with the first set of parallel grooves and optionally a third set of parallel grooves that at least partially intersect with the first and second sets of parallel grooves.
17. The decorative structure of claim 3, wherein the at least partially reflective layer is a reflective or semi-transparent layer that comprises a layer of silver and/or aluminium, or a plurality of layers of material forming a dielectric mirror.
18. The decorative structure of claim 1, wherein the grooves are triangular and have a depth of between 50 and 150 μm.
19. The decorative structure of claim 1, wherein at least some of the grooves comprise or are formed from a first planar wall and a second planar wall, wherein the angle between the first planar wall and the planar surface of the substrate is different to the angle between the second planar wall and the planar surface of the substrate.
20. The decorative structure of claim 7, wherein the plurality of grooves comprises a third set of parallel grooves that at least partially intersects with the first and second sets of parallel grooves.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0154] One or more embodiments of the invention will now be described, by way of example only, with reference to the appended drawings, in which:
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DETAILED DESCRIPTION
[0171] The present inventors have surprisingly discovered that a decorative structure having a macroscopically flat profile and having many of the optical characteristics of gemstones could be obtained by combining a planar support with a faceted microstructure and optionally an at least partially reflective layer. The decorative structure can be advantageously highly sheet-like or plate-like, having a relatively small thickness, while creating the illusion of depth through the faceted microstructure.
[0172]
[0173] The microstructure 24 comprises a plurality of grooves 28, 28′, which in the embodiment shown on
[0174] The grooves 28, 28′ create a continuous pattern of facets 30 (indicated by dashed lines on
[0175] The facets 30 comprise at least two different types of facets 30a, 30b, that differ by their geometry and/or their angle α.sub.a, α.sub.b relative to the planar major surface 22a of the support. In the embodiments shown on
[0176] In the embodiments shown on
[0177] In embodiments (not shown), the facets 30 may also be provided, which are parallel to the first planar major surface. Such facets are not formed by sections of the side walls 28a, 28, 28a′, 28b′ of the grooves, but may be formed from a top surface of the microstructure or a bottom surface of one or more type of groove which surfaces are parallel to the first planar major surface of the support. Advantageously, the combination of facets formed from the walls of the groove and facets parallel to the first planar major surface of the support may result in a microstructure that has a geometry similar to that of the crown of a gemstone, with a flat table surrounded by inclined facets. Where facets are present that are parallel to the first planar major surface of the support, facets formed from the walls of the grooves (i.e. facets that are inclined relative to the planar major surface of the support) advantageously cover an area of the microstructure that is approx. 3, 4, 10, 20, 50, 100, or 140 times larger than the area covered by facets that are parallel to the first planar surface of the support. In other words, the area obtained by projection of the inclined facets of the microstructure onto the first planar surface of the support is at least approx. 3, 4, 10, 20, 50, 100, or 140 times larger than the area obtained by projection of the parallel facets of the microstructure onto the first planar surface of the support. While the use of facets parallel to the first major surface of the support may contribute to generating a “gem-like” appearance (i.e. by obtaining a geometry similar to that of the crown of a classically cut gemstone), such facets may not generate optical effects that are as complex as those generated by inclined facets. As such, excessive areas covered by parallel facets may have a negative effect on the optical properties of the decorative structure, which may appear more “dull”.
[0178] In embodiments, the grooves 28, 28′ may have a depth of between 30 μm and 200 μm. Advantageously, this range of depth of grooves may enable to create inclined facets that have angles sufficiently high to create optical effects of interest such as fire and scintillation, while maintaining a size of facets that is sufficiently large to be distinguishable by the naked eye. Without wishing to be bound by theory, it is believed that the ability to distinguish facets with the naked eye is lost when the facets are smaller than about 300 μm at their widest point, thereby reducing the “gemstone-like” appearance of the structure. In preferred embodiments, the triangular grooves have a depth of between 50 μm and 150 μm. Such depths may be particularly amenable to production by imprint lithography. In embodiments, the triangular grooves have a depth of between 60 μm and 100 μm, such as about 90 μm.
[0179] The angles α.sub.a, α.sub.b, α.sub.c, α.sub.d between the planar walls and the first planar surface 22a of the support 22 may be individually selected between about 5 and about 35°. For example, the angles between the planar walls and the planar surface of the support may be individually selected between about 5° and about 25°, preferably between about 5° and about 15°. The angles between the planar walls and the planar surface of the support may be limited to about 25°, such as at most about 20°, or at most about 17.5°. As the skilled person would understand, the fire associated with a facet may be expected to be lower with shallower angles. However, steeper angles would result in smaller facets for a given depth of the groove, where the depth of the groove is limited by the thickness of the microstructure. Angles in the above ranges may advantageously enable the structure to have acceptable fire while maintaining a size of the facets that are formed from the walls of the grooves such that these are visible with the naked eye, without exceeding depths of about 200 μm. Facets with a width of at least about 300 μm may be considered to be sufficiently large to be distinguishable with the naked eye. In the context of this disclosure, the width of a facet refers to the length of the diameter of the smallest circle that would fit the geometry of the facet. In preferred embodiments, the facets of the microstructure have a width of at least about 350 μm. Advantageously, facets that are distinguishable by the naked eye may contribute to the “gem-like” visual impression of the decorative structure.
[0180] The at least partially reflective layer 26, where present, is configured to at least partially reflect light that is incident on and/or passes through the microstructure 24 from the viewing direction, i.e. reflecting light back towards the viewing direction. In the embodiment of
[0181] The at least partially reflective layer 26 may be a reflective (also referred to as “mirror” layer) or a semi-transparent layer, depending on the intended use of the decorative structure. For example, a semi-transparent (partially reflective) layer may be used when the decorative structure is intended to be used in a context where light may be predominantly or at least partially originating from behind the structure (i.e. the other side of the decorative structure from the viewing direction), such that the light should be able to pass through the decorative structure. For example, this may be the case when the decorative structure is used in architectural applications (e.g. when the decorative structure is or is applied to a room separator, e.g. a glass panel), or to form a decorative component of a lighting device where the light source is placed on the other side of the device from the viewing direction. A reflective (mirror) layer would be expected to provide a more pronounced optical effect because it would reflect more light than a semi-transparent layer. Therefore, a reflective layer may be preferably used in applications where there is no need for light to be able to pass through the structure from the side of the structure opposite the viewing direction. This may be the case in many decorative uses such as, for example, when the decorative structure is a decorative film for application on the surface of products. In some embodiments, for example, embodiments comprising multiple microstructures as will be explained further below, combinations of semi-transparent and reflective layers may be used.
[0182] A reflective or semi-transparent layer may be obtained by applying a layer of silver and/or aluminium, where the thickness of the layer may determine whether the layer is reflective or semi-transparent. For example, layers of silver or aluminium may be applied with a thickness of between about 20 nm and about 1 μm to obtain a reflective layer. Alternatively, a reflective or semi-transparent layer may be obtained by applying a plurality of layers of material forming a dielectric mirror.
[0183] The facets of the microstructure, and hence the walls of the grooves that form the facets are preferably surfaces with low surface roughness and high flatness. In the context of the present disclosure, a surface may be considered to have low surface roughness if it has a Ra<100 nm, where Ra is the arithmetic mean deviation of the surface profile, as known in the art. In the context of the present disclosure, a surface may be considered as having high flatness (also referred to as low waviness), if it has an average flatness deviation d.sub.r below 2 μm, where the flatness deviation is the maximum deviation from the intended plane of the surface, as known in the art. Preferably, the facets of the microstructure have a surface roughness Ra below about 50 nm, below about 20 nm, below about 10 nm, or below about 5 nm. In preferred embodiments, the facets of the microstructure have a flatness deviation d.sub.f below about 1 μm, below about 800 nm, below about 500 nm or below about 200 nm. Without wishing to be bound by theory, it is believed that surface roughness in excess of the above ranges may negatively impact the brilliance of the resulting microstructure and/or the fire of the resulting microstructure, due to the appearance of stray light rather than predictable consistent patterns of reflection, refraction and dispersion. Similarly, it is believed that high levels of flatness deviation may negatively impact the brilliance and/or fire of the resulting microstructure.
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[0185] In the embodiment shown in
[0186] In the embodiment shown in
[0187] While the embodiments shown in
[0188] The two superimposed microstructures preferably have different arrangements of facets, in order to increase the complexity of the optical effects created by the combination of microstructures. Different arrangements of facets can be obtained by using two microstructures that have different geometries (e.g. different configurations of triangular grooves), or similar (possibly identical) geometries that are superimposed such that the two microstructures are not aligned when viewed perpendicular to the main planes of the microstructures (i.e. from the viewing direction). For example, the two microstructures may have similar geometries that are rotated relative to each other. Advantageously, the use of different geometries or similar geometries that are not aligned increase the complexity of the geometric pattern created by the decorative structure, thereby increasing the “gem-like” appearance of the decorative structure.
[0189] In the embodiments shown in
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[0191] Further, in the embodiments shown in
[0192] As the skilled person would understand, all of the parallel grooves in each set may be symmetrical or asymmetrical grooves, and all of the grooves within a set may be configured so as to have the same or different angles between each of the planar walls forming each groove and the planar surface of the support.
[0193] In embodiments comprising multiple superimposed microstructures, the microstructures may be chosen to have different geometries that have the same fold symmetry. For example, two microstructures may be used that both have two-fold or three-fold symmetry, but which may vary by the distance between the grooves or the combination of angles between the walls of the grooves and the surface of the support on which the microstructure is applied. Advantageously, when the two microstructures have similar geometries or the same fold symmetry, the two microstructures may be rotated relative to each other by an angle that is not a rotational angle of symmetry of the microstructures. For example, when the microstructures have two-fold symmetry, the two microstructures may be rotated relative to each other by an angle that is not 90 or 180°. Similarly, when the microstructures have three-fold symmetry, the two microstructures may be rotated relative to each other by an angle that is not 60, 120 or 180°. For example, the two microstructures may be rotated relative to each other by an angle of about 25°.
[0194] In embodiments the grooves of each set may be spaced by between approx. 300 μm and 5,000 μm. In embodiments, the grooves may be spaced by between approx. 300 μm and approx. 2,500 μm. In embodiments, the spacing between grooves may be adapted depending on the depth of the grooves. For example, deeper grooves (thicker microstructures) may be more distant from each other. In embodiments, the grooves have a depth of about 90 μm and the grooves of each set are spaced by between approx. 300 μm and approx. 500 μm. In embodiments, the width of each groove may be between 300 μm and 2,500 μm etc.
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[0196] The support 22 is preferably made from a transparent material. Within the context of the present invention, a material is called transparent if it allows the transport of light, in particular at least visible light. Typically, the material is transparent in the conventional sense, i.e. allowing (at least visible) light to pass through the material without being scattered. As the skilled person would understand, the use of a transparent support may be particularly advantageous in embodiments such as those shown in
[0197] As the skilled person would understand, the material of the support may be selected depending on at least the intended application of the decorative structure. As such, the support can be made from a variety of materials. For example, the support may be made from a material selected from glass, such as crystal glass (e.g. crystal glass as defined by the European Crystal Directive (69/493/EEC) may be particularly advantageous due to their superior optical properties), ultrathin glass, chemically strengthened glass (such as e.g. Gorilla® Glass from Corning®), or an organic polymer such as PET (polyethylene terephthalate), PMMA (poly(methyl methacrylate)), or PE (polyethylene). As the skilled person would understand, the support may be made from a composite material comprising one or more materials selected from the above list, such as, for example, one or more layers of glass and/or one or more layers of polymers. Thus, the support may be a safety glass panel comprising two layers of glass separated by a layer of transparent elastomeric material.
[0198] ‘Glass’ in this context means any frozen supercooled liquid that forms an amorphous solid. Oxidic glasses, chalcogenide glasses, metallic glasses or non-metallic glasses can be employed. Oxynitride glasses may also be suitable. The glasses may be one-component (e.g. quartz glass) or two-component (e.g. alkali borate glass) or multi-component (e.g. soda lime glass) glasses. The glass can be prepared by melting, by sol-gel processes, or by shock waves. Such methods are known to the skilled person. Inorganic glasses, especially oxidic glasses, are preferred. These include silicate glasses, soda lime glasses, borate glasses or phosphate glasses. Lead-free crystal glasses are particularly preferred. In embodiments, silicate glasses are preferred. Silicate glasses have in common that their network is mainly formed by silicon dioxide (SiO.sub.2). By adding further oxides, such as alumina or various alkali oxides, alumosilicate or alkali silicate glasses are formed. If phosphorus pentoxide or boron trioxide is the main network former of a glass, it is referred to as a phosphate or borate glass, respectively, whose properties can also be adjusted by adding further oxides. The mentioned glasses mainly consist of oxides, which is why they are generically referred to as oxidic glasses. In embodiments, the support may be made of lead and barium-free crystal glass. Examples of suitable lead and barium-free crystal glass compositions for use in the present invention are disclosed in EP 1725502 and EP 2625149, the contents of which are incorporated herein by reference.
[0199] In embodiments, the support is made of plastic. Transparent plastics are preferred. Among others, the following materials are suitable: acrylic glass (polymethyl methacrylates, PMMA); polycarbonate (PC); polyvinyl chloride (PVC); polystyrene (PS); polyphenylene ether (PPO); polyethylene (PE); polyethylene therephtalate (PET), and poly-N-methylmethacrylimide (PMMI).
[0200] An advantage of using a plastics material over glass in the manufacture of supports for use in the present invention resides, in particular, in the lower specific weight, which is only about half that of glass. In addition, other material properties may also be selectively adjusted. Further, plastics are often more readily processed as compared to glass. Some disadvantages of the use of plastics materials include the low modulus of elasticity and the low surface hardness as well as the massive drop in strength at temperatures from about 70° C. and above, as compared to glass.
[0201] In embodiments, the support is a substantially flat structure, such as e.g. a panel, sheet or film of material. For example, the support may be a flexible film of material. The support may be a film made from an organic polymer such as PET, PMMA or PE. In some such embodiments, the film has a thickness of at most 2 mm, at most about 1 mm, at most about 500 μm, between about 100 μm and about 200 μm, or suitably about 125 μm. In some embodiments, the decorative structure may have a weight below 1 kg/m.sup.2, preferably below 500 g/m.sup.2, such as about 250 g/m.sup.2. Lightweight films may advantageously be applied on large surfaces and/or light articles without negatively impacting the properties of the articles to which the film is applied.
[0202] The microstructure is also preferably made from a transparent material. Advantageously, the use of a transparent material enables visible light to travel through the material of the microstructure such that it can be at least partially reflected by the at least partially reflective layer, where the combination of faceting and reflection results in patterns of refraction that are similar to those created by a gemstone. Preferably, the microstructure is made from a material that is non-diffusive. Within the context of the invention, a material may be considered as non-diffusive if it exhibits mostly specular reflection. Beneficially, a non-diffusive material does not exhibit any diffusive reflection, or only exhibits very low levels of diffusive reflection, such that the material does not appear as milky or turbid. The microstructure may advantageously be made from a material that has high optical dispersion.
[0203] In the context of the present invention, a material may be considered to have high optical dispersion if it shows a high variation of refractive index as a function of wavelength in the visible range. For example, a material may be considered to have a high optical dispersion if it has a low Abbe number, such as an Abbe number below about 60, preferably below about 50, below about 40 or below about 35. Advantageously, the use of a material with high optical dispersion may increase the colour split that occurs when white light interacts with the facets of the structure. This may in turn improve the fire of the structure for a given maximum angle of facets. Without wishing to be bound by theory, it is believed that the fire of the structure is influenced by the optical dispersion of the material of the microstructure as well as the angles of the facets (formed by the walls of the grooves) relative to the plane of the structure. Sharper facets are expected to improve fire, as would higher dispersion. Therefore, a given requirement, e.g. in relation to the fire exhibited by the structure, may be achievable by balancing at least these two parameters. For example, in embodiments where shallow facets are preferred, materials with higher dispersion may be chosen compared to embodiments using facets at steeper/sharper angles of inclination to the planar surface of the support. The Abbe number of a material may be determined, for example, by ellipsometry, as known in the art. In particular, the refractive index of the material at multiple wavelengths at least within the visible range may be measured, for example, using variable angle spectroscopic ellipsometry, and the Abbe number may be calculated as v=(nd−1)/(nF−nC) where nd, nF and nC are the refractive indices of the material at the wavelengths of the Fraunhofer d− (He light source), F− (H light source) and C− (H light source) spectral lines (587.56 nm, 486.13 nm and 656.27 nm respectively) or v=(ne−1)/(nF′−nC′), where ne, nF′ and nC′ are the refractive indices of the material at the wavelengths of the Fraunhofer e− (Hg light source), F′− (Cd light source) and C′− (Cd light source) spectral lines (546.07 nm, 479.99 nm and 643.86 nm respectively).
[0204] In embodiments, the microstructure is made from any polymer that is suitable for imprinting, as known in the art. In embodiments, the microstructure is made from hybrid polymers. In embodiments, the microstructure is made from UV-curable or thermally curable paints. In embodiments, the microstructure is made from a thermosetting material, such as e.g. sol-gel or polycarbonate. The microstructure may be made from a material obtained by curing a curable resin composition, for example, a UV curable resin composition. This may enable the microstructure to be provided by forming a resin composition in a plastic state then curing it to obtain a substantially solid structure. In embodiments, the UV curable resin composition comprises acrylate and/or methacrylate monomers, and has a high aromatic content, as will be explained further below. In the context of the invention, a composition may be considered to have a high aromatic content if the composition has an aromatic content of at least about 40%, preferably at least about 50%. The aromatic content of a compound or composition may be quantified as the proportion of the carbon atoms in the compound or composition that are part of aromatic rings. Advantageously, the use of UV curable resin compositions with a high aromatic content may be associated with high refraction indices and high dispersion, compared to commonly used imprinting resins. As explained above, this may contribute to increasing the fire of the decorative structure.
[0205] The decorative structure may further comprise a decorative coating applied on at least a region of the microstructure. Any decorative coating that is at least semi-transparent may be used in the present invention. For example, a decorative coating may be configured to give a coloured appearance to the region of the microstructure on which it is applied. Colouring and decorative coatings may enable the decorative element to be provided with a variety of decorative effects, improving their flexibility of use. In embodiments, a decorative coating may be configured to provide a complex decorative optical effect on the region of the microstructure on which it is applied. These can be achieved using a multi-layer interference system (such as e.g. alternating layers of TiO.sub.2 and SiO.sub.2) that creates a desired optical effect, using a multi-layer system (such as e.g. alternating thin layers of Fe.sub.2O.sub.3 and Cr) that creates a desired optical effect by causing a wavelength-specific ratio of transmission and reflection of light; or using a multi-layer system that creates a desired optical effect by causing a wavelength-specific absorption and reflection of visible light such that some wavelengths are intensely reflected while others are absorbed. The layers of the multi-layer systems described above may be deposited by any PVD or CVD method known in the art, such as e.g. by sputtering.
[0206] The support and/or the microstructure may be coloured. For example, a colouring agent may be provided throughout the body of the support and/or the microstructure. For example, when the support is made of glass or crystal glass, a colouring can be achieved by introducing metal oxides in the glass. Alternatively or in addition to colouring the material of the support or the microstructure, a colouring may be provided as a coating or other surface treatment on at least a region of the support or the microstructure.
[0207] The decorative structure may further comprise a backing layer. For example, a backing layer may be provided in combination with a reflective layer, on the side of the reflective layer that is opposite from the microstructure(s).
[0208] In embodiments, the backing layer may comprise a protective layer. A protective layer may advantageously protect the decorative structure, and in particular the reflective layer on the decorative structure, from mechanical and/or chemical damage.
[0209] In embodiments, the backing layer comprises a protective layer and one or more adhesive layer(s), at least one of the one or more adhesive layers being provided on the side of the backing layer that is exposed in the finished decorative structure.
[0210] The protective layer may comprise a layer of lacquer. In embodiments, the layer of lacquer comprises a lacquer selected from the group consisting of: epoxy lacquers, one component polyurethane lacquers, bi-component polyurethane lacquers, acrylic lacquers, UV-curable lacquers, and sol-gel coatings. The lacquer may optionally be pigmented. Lacquer may be applied by any method known in the art, such as by spraying, digital printing, rolling, curtain coating or other two-dimensional application methods known in the art. Suitably, the lacquer may be selected so as to be mechanically and chemically robust and bondable. In embodiments, a lacquer is mechanically and chemically robust if it would not substantially degrade or allow degradation of an underlying reflective layer in the conditions that would be expected in the intended use. For example, the decorative structure may advantageously show high resistance to any of sweat, machine washing, temperature changes, sun exposure test, and suitable performance in anti-corrosion salt spray and climate tests. Resistance to machine washing may be tested by subjecting a sample of the decorative structure to 10 cycles of machine washing at 40° C., optionally followed by drying, and examining the decorative structure for any visible damage, with the naked eye. Suitable performance in climate tests may be tested by exposing a sample of the decorative structure to climate tests (e.g. exposure to the environment or a simulated environment) for 480 hours, and examining the decorative structure for any visible damage, with the naked eye. Resistance to sweat may be tested by putting a sample of the decorative structure in contact with artificial sweat for 48 hours, and examining the sample for any visible damage, with the naked eye. Resistance to temperature changes may be tested by subjecting a sample of the decorative structure to 20 cycles of temperature changes, and examining the sample for any visible damage, with the naked eye. For example, a cycle of temperature changes may comprise exposing the decorative element to a temperature of about 70° C., followed by a sudden transfer to −20° C., then to room temperature (such as e.g. between 20 and 25 °C.). Resistance to sun exposure may be tested by subjecting a sample of the decorative structure to a simulated solar energy of 13.8 MJ/m.sup.2 and examining the decorative element for any visible damage, with the naked eye. For example, the sample may be subjected to light between about 300 and about 800 nm at about 650 W/m.sup.2 for a period of about 48 to 72 hours, such as about 62.8 hours. Suitable performance in anti-corrosion salt spray may be tested by exposing a sample of the decorative element to sea water tests for 96 hours, and examining the sample for any visible damage, with the naked eye. The lacquer may additionally ensure that the decorative structure according to the invention is bondable. As the skilled person would understand, the choice of a suitable lacquer may depend on the material to which the decorative element is intended to be bonded, and/or on the adhesive that is intended to be used. Lacquer may be applied with a thickness of between about 4 and 14 μm (i.e. 9±5 μm); for example, the lacquer may be applied with a thickness of about 9 μm.
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[0212] At step 700, a master stamp for imprinting is provided. A master stamp is typically a metallic structure that can be used to replicate a pattern onto a working stamp. For example, a nickel or nickel phosphorus stamp may be used. Providing a metallic master stamp comprises creating a plurality of triangular grooves in a metal substrate using a monocrystalline diamond cutting tool. Advantageously, the use of a monocrystalline diamond cutting tool may enable to create a metal master stamp that has very low surface roughness and high flatness, thereby ultimately resulting in a microstructure that has low surface roughness and high flatness and, as such, better optical properties. Preferably, the master stamp has a surface roughness Ra below about 100 nm, preferably below about 50 nm, below about 20 nm, below about 10 nm, or below about 5 nm. Advantageously, the master stamp has a flatness deviation d.sub.f below about 2 μm, preferably below about 1 μm, below about 800 nm, below about 500 nm or below about 200 nm. The monocrystalline diamond cutting tool may be chosen to have a symmetrical triangular shape, to create grooves as shown on
[0213] The plurality of triangular grooves may comprise a first set of parallel grooves and a second set of parallel grooves that at least partially intersects with the first set of parallel grooves, as explained above in relation to
[0214] In embodiments where first and second microstructures are formed, the first and second microstructures may be formed using the same or different stamps, depending on the geometries of the microstructures, as explained above. As the skilled person would understand, when the microstructures are moulded or provided by filling cavities in microstructured reflective metal sheets, the first and second microstructures may similarly be formed using the same or different stamps moulds/microstructured reflective metallic sheets.
[0215] At step 710, one or more working stamp(s) are produced by replicating the metallic master stamp into a polymeric stamp material, or, for example, by replicating the metallic master stamp by galvanic replication. Any polymeric stamp material suitable for use in nanoimprinting technologies may be used in the present invention. In particular, the working stamps may be made of PDMS (polydimethylsiloxane), or using a polyurethane-acrylate resin, for example, a UV curable polyurethane-acrylate resin. Alternatively, where galvanic replication is used, the working stamps may be made of nickel or nickel phosphorus. The working stamp preferably has low surface roughness and high flatness. For example, the working stamp may have a surface roughness Ra below about 100 nm, preferably below about 50 nm, below about 20 nm, below about 10 nm, or below about 5 nm. Beneficially, the working stamp has a flatness deviation d.sub.f below about 2 μm, preferably below about 1 μm, below about 800 nm, below about 500 nm or below about 200 nm.
[0216] At step 720, a support is provided. The support has a first planar major surface and a second planar major surface opposite the first planar major surface, and may be as described above. The support may be provided on a roll or on a plate, depending for example on the configuration and materials of the support.
[0217] At step 730, a layer of imprintable material such as a curable resin is applied on the first planar major surface of the support. Applying a layer of imprintable material onto the first planar major surface of the support may be performed using a roller. The thickness of the layer of imprintable material may be between about 30 μm and about 200 μm, such as between about 50 μm and about 150 μm. The maximum thickness of the layer that can be applied may depend on the properties of the curable resin, and may in particular be limited by the penetration depth of radiations used to cure the resin.
[0218] At step 740, the layer of imprintable material is imprinted using the working stamp, for example, provided on a roller. At the same time or shortly thereafter, the imprintable material is cured. For example, when the imprintable material is a light (e.g. UV) curable resin, the resin may be cured through the stamp and/or through the support by exposing the resin to electromagnetic (e.g. UV) radiation. Preferably, the imprintable material is cured at the same time as imprinting, in order to reduce the risk of reflow of the imprintable material and/or the risk of the imprintable material adhering to the stamp. Preferably, the imprinting material is cured at least partially by exposing the imprintable material to electromagnetic radiation through the support. This may advantageously remove requirements on the stamp to be transparent to the electromagnetic radiation used. In such embodiments, the support is preferably transparent to the electromagnetic radiation in a wavelength range suitable to cure the imprintable material (e.g. allowing at least about 50%, at least about 70%, at least about 80%, at least about 90%, at least about 95% or at least about 98% of the radiation within the desired wavelength range to pass through the substrate). Such embodiments may be particularly suitable for use in embodiments where a transparent substrate (such as e.g. various polymeric films or plates, glass plates etc.) is desirable. As the skilled person would understand, the method of curing may depend on the imprintable material. In particular, different materials may require different conditions (temperature, humidity, radiations) to cure. Further, some materials may not cure but instead solidify, in which case the material may be imprinted then allowed to solidify. The curable resin may be chosen as a UV curable resin, such as a UV curable resin as described further below. In embodiments, the microstructure is formed by thermal imprinting.
[0219] At step 750, an at least partially reflective layer may optionally be applied. As explained above, the at least partially reflective layer may be provided on the microstructure and/or on the first or second planar major surface of the support. As such, step 750 may be performed prior to forming the microstructure or after a second layer of curable resin as been formed. The at least partially reflective layer may have any of the properties explained above. In particular, the one or more layers forming the at least partially reflective layer may be applied by physical vapour deposition (PVD) or chemical vapour deposition (CVD).
[0220] In embodiments, the method further comprises applying a decorative coating on the microstructure, as explained above.
[0221] According to the depicted embodiment, at step 760 which is an optional step), a second layer of imprintable material is provided, either on the second planar major surface of the support, or on the previously formed, cured and coated microstructure. In embodiments, the second layer of imprintable material is imprinted and cured 770, in a similar way as step 740. As explained above, step 770 may use the same or a different stamp from step 740. Further, it may be advantageous for the support to be rotated relative to the working stamp before imprinting at step 770, in order to produce complex optical effects arising from the combination of superimposed microstructures, as explained above.
[0222] In other embodiments (not shown), forming a microstructure may comprise providing a mould having concavo-convex structures that are configured to form the grooves of the microstructure, combining the support with the mould, and injecting a polymeric material in the space between the mould and the support. In such embodiments, the support and microstructure may be formed at the same time and/or integrally, for example, using simultaneous injection moulding or injection-compression moulding of plastics. The mould advantageously has a surface roughness Ra below about 100 nm, preferably below about 50 nm, below about 20 nm, below about 10 nm, or below about 5 nm. In embodiments, the mould has a flatness deviation d.sub.f below about 2 μm, preferably below about 1 μm, below about 800 nm, below about 500 nm or below about 200 nm.
[0223] Alternatively, forming a microstructure may comprise providing a microstructured reflective metallic sheet having concavo-convex structures configured to form the grooves of the microstructure, and assembling the microstructured reflective metallic sheet with the support using a polymeric material that substantially fills the grooves between the triangular structures of the metallic sheet. A microstructured reflective metallic sheet may be provided by deep drawing a metallic sheet to create concavo-convex structures, such as, for example, triangular structures. Beneficially, the microstructured reflective metallic sheet has a surface roughness Ra below about 100 nm, preferably below about 50 nm, below about 20 nm, below about 10 nm, or below about 5 nm. Beneficially, the microstructured reflective metallic sheet has a flatness deviation d.sub.f below about 2 μm, preferably below about 1 μm, below about 800 nm, below about 500 nm or below about 200 nm. The concavo-convex structures may have a height of between about 30 μm and about 200 μm.
[0224] According to a further aspect of the present disclosure, a UV curable resin composition is provided which is suitable for making a decorative structure as described. The UV curable resin composition comprises acrylate and/or methacrylate monomers and a photoinitiator, wherein the composition has an aromatic content of at least about 50%. Advantageously, the use of UV curable resin compositions with a high aromatic content may be associated with high refraction indices and high dispersion, compared to commonly used nanoimprint resins. This may be particularly advantageous for use in creating decorative structures according to the invention, where high dispersion creates desirable optical effects.
[0225] In embodiments, the curable resin composition has a viscosity below about 3 Pas. In embodiments, the composition has a viscosity between about 500 mPas and about 3,000 mPas. In embodiments, the curable resin composition has a viscosity between about 500 mPas and about 1,500 mPas, preferably between 500 mPas and 1,000 mPas, such as e.g. between 700 mPas and 1,000 mPas. Advantageously, resins with a pre-cured viscosity in the above ranges may be conveniently applied as thin uniform coating films. For example, the resin compositions according to the invention may have a pre-cured viscosity such that the compositions can be applied in layers of between about 15 μm and about 200 μm. This may be particularly advantageous for use in nanoimprint lithography.
[0226] In embodiments, the composition comprises methacrylate monomers as a main component. For example, methacrylate monomers may form at least about 90%, at least about 92%, at least about 94%, at least about 96%, at least about 97% or at least about 98% of the curable resin composition by weight. Without wishing to be bound by theory, it is believed that methacrylates are less likely to be a cause of skin irritation than acrylates, and as such may be desirable in some applications. In embodiments, the composition comprises acrylate monomers as a main component. For example, acrylate monomers may form at least about 90%, at least 92%, at least 94%, at least 96% or at least 98% of the curable resin composition. Without wishing to be bound by theory, it is believed that faster polymerisation speeds can be obtained using acrylate monomers than methacrylate monomers, due to higher radical polymerisation reactivity of acrylates. As such, acrylate monomers may be associated with higher production speeds, and may be advantageous in some applications.
[0227] In embodiments, the resin composition, when cured, results in a polymer material that is transparent. In embodiments, the resin composition, when cured, results in a polymer material that has high optical dispersion. In embodiments, a polymer material with high optical dispersion has a low Abbe number, such as an Abbe number below about 60, preferably below about 50, below about 40 or below about 35.
[0228] In embodiments, the photoinitiator is a photoinitiator with a high UV-A absorption coefficient, such as e.g. at least about 300, at least about 400, and preferably at least about 500 L/(mol*cm) at wavelengths between 350 nm and 400 nm. In embodiments, the photoinitiator is a photoinitiator with low absorption in the visible wavelengths, such as e.g. below about 300 L/(mol*cm), below about 250 L/(mol*cm), and preferably below about 200 L/(mol*cm) at wavelengths between 400 and 700 nm. Preferably, the photoinitiator is liquid at room temperature. Advantageously, high absorption in the UV-A range may contribute to a rapid polymerisation, while low absorption in the visible range may make the resin composition more stable and convenient to manipulate prior to exposure to UV for curing.
[0229] Suitable photoinitiators for use according to the invention include ethyl(2,4,6-trimethylbenzoyl)-phenyl phosphinate (cas no. 84434-11-7, TPO-L, available from IGM), blends of bis(2,6-dimethoexybenzoyl)-2,4,4-trimethyl pentylphosphineoxide and 1-hydroxy-cyclohexyl-phenyl-ketone (such as that available as Genocure LTM), 2,4,6-Trimethylbenzoyldiphenylphosphine oxide (available as Genocure TPO), Benzil dimethyl ketal 2,2-methoxy-1,2-diphenyl ethanone (available as Genocure BDK, also available as Irgacure 651), 2-hydroxy-2-methyl-1-phenyl-propan-1-one (available as Genocure DMHA), 1-hydroxycyclohexyl phenyl ketone (available as Irgacure 184), and blends of 1-hydroxy-cyclohexylphenyl-ketone and benzophenone (such as that available as Additol BCPK). Amongst these, compounds such as those in TPO-L, Irgacure 184, DMHA and Additol BCPK may be advantageous as they may be result in transparent cured resin layers even when the resin layer is as thick as 100 to 200 μm. Further, blends such as that available as Additol BCPK may result in a resin that has increased adhesion to substrates, such as e.g. PET or PE, when cured.
[0230] In embodiments, the photoinitiator is present in a concentration of at most about 3% by weight of the curable resin composition. In embodiments, the photoinitiator is present in a concentration of at least about 0.1% by weight of the curable resin composition, preferably between about 0.5 and 3%, such as about 1%, about 1.5% or about 2% of the total weight of the curable resin composition. Advantageously, the amount of photoinitiator may be chosen such that substantially complete crosslinking of the polymer can be achieved in the curing conditions used. Indeed, incomplete crosslinking may reduce the stability (e.g. mechanical stability) of the cured resin, and non-reacted groups that may still be present in the non-fully cured resin may cause e.g. skin irritation. As the skilled person would understand, the degree to which complete crosslinking of the polymer is achieved may depend on the concentration of the photoinitiator as well as the emission spectrum and power of the UV lamp used, and the exposure time. As such, depending on the particular curing process used, the optimal amount of photoinitiator may vary. The present inventors have found that the above ranges of photoinitiator concentrations typically resulted in adequate crosslinking at least in their curing process (below 1s polymerisation time upon UV exposure 1W/cm.sup.2 at wavelengths between 350 nm and 400 nm, such as 365 nm to 395 nm). As the skilled person would understand, including concentrations of photoinitiator that are higher than necessary for complete cross linking may result in the presence of unbound photoinitiator in the cured resin. This may be disadvantageous as it reduces the amount of “useful” (i.e. curable) polymer in the resin composition, and represents a waste of photoinitiator.
[0231] In embodiments, the (meth)acrylate monomers represent at least about 90% by weight of the curable resin composition, preferably about 95%, about 96%, about 97%, about 98% of about 99% of the total weight of the curable resin composition. In embodiments, the composition comprises about 98% by weight of the curable resin composition of (meth)acrylate monomers, and about 2% by weight of the curable resin composition of photoinitiator. In embodiments, the composition comprises at least about 96% by weight of the curable resin composition of (meth)acrylate monomers, and at most about 3% by weight of the curable resin composition of photoinitiator. In embodiments, the composition comprises at least about 97% by weight of the curable resin composition of (meth)acrylate monomers, and at most about 2% by weight of the curable resin composition of photoinitiator.
[0232] In embodiments, the composition comprises a first type of (meth)acrylate monomers that are at least bifunctional and lead to spatial crosslinking upon curing, and a second type of (meth)acrylate monomers that have very high aromatic content. For example, the second type of (meth)acrylate monomers may have an aromatic content of at least about 50%, at least about 60% or at least about 70%. In embodiments, substantially all of the (meth)acrylate monomers in the composition are either of the first or second type. In embodiments, the second type of (meth)acrylate monomers may form chains (i.e. no cross-linking) upon curing. In embodiments, the second type of (meth)acrylate monomers may be monofunctional. Advantageously, the second type of (meth)acrylate monomers may have a viscosity at room temperature below that of the first type of (meth)acrylate monomers. In embodiments, the second type of (meth)acrylate monomers may have a viscosity at room temperature below about 200 mPas. In embodiments, the first type of (meth)acrylate monomers may have a viscosity at room temperature above about 1,000 mPas. In embodiments, the second type of (meth)acrylate monomers may have a refractive index of at least about 1.51.
[0233] The present inventors have discovered that by combining (meth)acrylate monomers of the first and second type, it was possible to obtain a UV curable resin composition that, when cured, has good thermal, mechanical and/or chemical stability combined with a high refractive index and high dispersion, and that prior to curing, has adequate viscosity for applying as a thin layer (for example, by roller based coating). Without wishing to be bound by theory, it is believed that the (meth)acrylate monomers of the first type may contribute to the thermal, mechanical and/or chemical stability of the cured resin, while the (meth)acrylate monomers of the second type may contribute to increasing the refractive index and dispersion of the cured resin, and lowering the viscosity of the uncured resin.
[0234] Suitable monomers for use as a second type of monomers may include ortho-phenyl-phenol-ethyl-acrylate (available as MIWON Miramer M1142, refractive index RI(ND25)=1,577, viscosity at 25° C.=110-160 mPas) and 2-phenoxyethyl-acrylate (available as MIWON Miramer M140, refractive index RI(ND25)=1,517, viscosity at 25° C.=10-20 mPas). Further suitable monomers for use as a second type of monomers may include phenylepoxyacrylate (available as MIRAMER PE 110), benzylacrylate (available as MIRAMER M1182), benzylmethacrylate (available as MIRAMER M1183), phenoxybenzylacrylate (available as MIRAMER M1122) and 2-(phenylthio)ethylacrylate (available as MIRAMER M1162). In preferred embodiments, the composition comprises ortho-phenyl-phenol-ethyl-acrylate as the only monomer of the second type.
[0235] In embodiments, the first type of (meth)acrylate monomers may have a refractive index of at least about 1.51. Suitable monomers for use as a first type of monomers include ethoxylated(3)bisphenol-A-dimethacrylate (available as Sartomer SR348C, refractive index RI(ND25)=1,53), and aromatic urethane diacrylate oligomers such as Allnex Ebecryl 210 (E210) (refractive index approx. RI(ND25)=1,52). Further suitable monomers for use as a first type of monomers include ethoxylated (2)bisphenol-A-dimethacrylate (available as Sartomer SR348L, viscosity at 60°=1,600 mPas, refractive index similar to that of ethoxylated(3)bisphenol-A-dimethacrylate), ethoxylated (3)bisphenol-A-diacrylate (available as Sartomer SR349 or Miwon MIRAMER 244), ethoxylated (4)bisphenol-A-diacrylate (available as Miwon MIRAMER M240), bisphenol-A-diepoxyacrylate (available as Miwon MIRAMER PE210, viscosity at 60°=5000 mPas), bisphenol-A-diepoxymethacrylate (available as Miwon MIRAMER PE250, viscosity at 60°=5,000 mPas). In preferred embodiments, the first type of (meth)acrylate monomers may be selected to have a viscosity at 60° below about 3,000 mPas, preferably below about 2,000 mPas. In preferred embodiments, the curable resin composition comprises ethoxylated(3)bisphenol-A-dimethacrylate as the only monomer of the first type.
[0236] In embodiments, the curable resin composition comprises one or more (meth)acrylate monomers of the first type and one or more (meth)acrylate monomers of the second type. In embodiments, the UV curable resin composition comprises proportions of (meth)acrylate monomers of the first and second type between about 1:1 and 1:3 by weight (i.e. one part monomers of the first type to between 1 and 3 parts monomers of the second type); such as about 1:2. In other words, the UV curable resin composition may comprise at least as much of the monomers of the second type (by weight) as of the monomers of the first type, and in some embodiments a higher amount by weight of the monomers of the second type compared to the amount by weight of monomers of the first type. In embodiments, the curable resin composition comprises at least about 15%, such as at least about 20% by weight (meth)acrylate monomers of the first type, and (meth)acrylate monomers of the second type up to a total percentage by weight of (meth)acrylate monomers of at least about 90%, at least 95%, at least 96%, at least 97%, or about 98% by weight. In embodiments, the curable resin composition comprises between 10 and 35% by weight of (meth)acrylate monomers of the first type, preferably between about 15% and about 30% by weight of the curable resin composition, such as about 25%. In embodiments, the curable resin composition comprises between about 35% and about 85% by weight of (meth)acrylate monomers of the second type, such as at least about 40% by weight of the curable resin composition. As the skilled person would understand, the proportions of monomers of the first and second types may be adjusted in order to adapt the exact properties of the curable resin composition and/or the cured resin to the intended use. For example, within the ranges described, it may be advantageous to increase the proportion of monomers of the first type to obtain a stiffer and chemically more stable cured resin, and conversely the proportion of monomers of the first type may be reduced to obtain a more flexible/elastic (albeit possibly chemically less stable) cured resin.
[0237] In embodiments, the UV curable resin composition has a curing (polymerisation) time of 1 second or less when exposed to UV light in the appropriate wavelength range (e.g. 350-400 nm, such as 365/395 nm) with a power of at least 1 W/cm.sup.2.
[0238] In embodiments, the UV curable resin composition comprises ethoxylated (3)bisphenol-A-dimethacrylate (first type of monomer) and ortho-phenyl-phenol-ethyl-acrylate (second type of monomer) as major components. In some such embodiments, the UV curable resin composition comprises a combined amount of ethoxylated (3)bisphenol-A-dimethacrylate and ortho-phenyl-phenol-ethyl-acrylate of at least about 90%, at least 92%, at least 93%, at least 94%, 95%, 96%, 97%, 98% or 99% by weight of the curable resin composition. In some such embodiments, the proportion of ethoxylated (3)bisphenol-A-dimethacrylate to ortho-phenyl-phenol-ethyl-acrylate is between about 1:1 and 1:3; such as about 1:2 (i.e. the amount by weight of ortho-phenyl-phenol-ethyl-acrylate is twice the amount by weight of ethoxylated (3)bisphenol-A-dimethacrylate). In some such embodiments, the UV curable resin composition further comprises ethyl(2,4,6-trimethylbenzoyl)-phenyl phosphinate, such as in a concentration of about 0.1 to 2% by weight of the curable resin composition. In some such embodiments, the UV curable resin composition further comprises a surfactant, such as e.g. 1H,1H,5H-octafluoropentyl-acrylate or a polyether-modified poly-dimethylsiloxane, as discussed below.
[0239] In embodiments, the UV curable resin composition comprises ethoxylated (2)bisphenol-A-dimethacrylate (first type of monomer) and ortho-phenyl-phenol-ethyl-acrylate (second type of monomer) as major components. In some such embodiments, the UV curable resin composition comprises a combined amount of ethoxylated (2)bisphenol-A-dimethacrylate and ortho-phenyl-phenol-ethyl-acrylate of at least about 90%, at least 92%, at least 93%, at least 94%, 95%, 96%, 97%, 98% or 99% by weight of the curable resin composition. In some such embodiments, the proportion of ethoxylated (2)bisphenol-A-dimethacrylate to ortho-phenyl-phenol-ethyl-acrylate is between about 1:1 and 1:3; such as about 1:2 (i.e. the amount by weight of ortho-phenyl-phenol-ethyl-acrylate is twice the amount by weight of ethoxylated (2)bisphenol-A-dimethacrylate). In some such embodiments, the UV curable resin composition further comprises ethyl(2,4,6-trimethylbenzoyl)-phenyl phosphinate, such as in a concentration of about 0.1 to 2% by weight of the curable resin composition. In some such embodiments, the UV curable resin composition further comprises a surfactant, such as e.g. 1H,1H,5H-octafluoropentyl-acrylate or a polyether-modified poly-dimethylsiloxane, as discussed below.
[0240] In embodiments, the UV curable resin composition comprises ethoxylated (3)bisphenol-A-dimethacrylate (first type of monomer) and 2-phenoxyethyl-acrylate (second type of monomer) as major components. In some such embodiments, the UV curable resin composition comprises a combined amount of ethoxylated (3)bisphenol-A-dimethacrylate and 2-phenoxyethyl-acrylate of at least 90%, at least 92%, at least 93%, at least 94%, 95%, 96%, 97%, 98% or 99% by weight of the curable resin composition. In some such embodiments, the proportion of ethoxylated (3)bisphenol-A-dimethacrylate to 2-phenoxyethyl-acrylate is between about 1:1 and 1:3, preferably about 1:2 (I.e. the amount by weight of 2-phenoxyethyl-acrylate is twice the amount by weight of ethoxylated (3)bisphenol-A-dimethacrylate). In some such embodiments, the UV curable resin composition further comprises ethyl(2,4,6-trimethylbenzoyl)-phenyl phosphinate, such as in a concentration of about 0.1 to 2% by weight of the curable resin composition. In some such embodiments, the UV curable resin composition further comprises a surfactant, such as e.g. 1H,1H,5H-octafluoropentyl-acrylate or a polyether-modified poly-dimethylsiloxane, as discussed below.
[0241] In embodiments, the UV curable resin composition comprises ethoxylated (2)bisphenol-A-dimethacrylate (first type of monomer) and 2-phenoxyethyl-acrylate (second type of monomer) as major components. In some such embodiments, the UV curable resin composition comprises a combined amount of ethoxylated (2)bisphenol-A-dimethacrylate and 2-phenoxyethyl-acrylate of at least about 90%, at least 92%, at least 93%, at least 94%, 95%, 96%, 97%, 98% or 99% by weight of the curable resin composition. In some such embodiments, the proportion of ethoxylated (2)bisphenol-A-dimethacrylate to 2-phenoxyethyl-acrylate is between 1:1 and 1:3; such as about 1:2 (i.e. the amount by weight of 2-phenoxyethyl-acrylate is twice the amount by weight of ethoxylated (2)bisphenol-A-dimethacrylate). In some such embodiments, the UV curable resin composition further comprises ethyl(2,4,6-trimethylbenzoyl)-phenyl phosphinate, such as in a concentration of about 0.1 to 2% by weight of the curable resin composition. In some such embodiments, the UV curable resin composition further comprises a surfactant, such as e.g. 1H,1H,5H-octafluoropentyl-acrylate or a polyether-modified poly-dimethylsiloxane, as discussed below.
[0242] In embodiments, the UV curable resin composition comprises ethoxylated (3)bisphenol-A-diacrylate (first type of monomer) and ortho-phenyl-phenol-ethyl-acrylate (second type of monomer) as major components. In some such embodiments, the UV curable resin composition comprises a combined amount of ethoxylated (3)bisphenol-A-diacrylate and ortho-phenyl-phenol-ethyl-acrylate of at least about 90%, at least 92%, at least 93%, at least 94%, 95%, 96%, 97%, 98% or 99% by weight of the curable resin composition. In some such embodiments, the proportion of ethoxylated (3)bisphenol-A-diacrylate to ortho-phenyl-phenol-ethyl-acrylate is between about 1:1 and 1:3, such as about 1:2 (I.e. the amount by weight of ortho-phenyl-phenol-ethyl-acrylate is twice the amount by weight of ethoxylated (3)bisphenol-A-dicrylate). In some such embodiments, the UV curable resin composition further comprises ethyl(2,4,6-trimethylbenzoyl)-phenyl phosphinate,such as in a concentration of about 0.1 to 2% by weight of the curable resin composition. In some such embodiments, the UV curable resin composition further comprises a surfactant, such as e.g. 1H,1H,5H-Octafluoropentyl-acrylate or a polyether-modified poly-dimethylsiloxane, as discussed below.
[0243] In embodiments, the UV curable resin composition comprises ethoxylated (3)bisphenol-A-diacrylate (first type of monomer) and 2-phenoxyethyl-acrylate (second type of monomer) as major components. In some such embodiments, the UV curable resin composition comprises a combined amount of ethoxylated (3)bisphenol-A-diacrylate and 2-phenoxyethyl-acrylate of at least about 90%, at least 92%, at least 93%, at least 94%, 95%, 96%, 97%, 98% or 99% by weight of the curable resin composition. In some such embodiments, the proportion of ethoxylated (3)bisphenol-A-diacrylate to 2-phenoxyethyl-acrylate is between about 1:1 and 1:3; such as about 1:2 (i.e. the amount by weight of 2-phenoxyethyl-acrylate is twice the amount by weight of ethoxylated (3)bisphenol-A-diacrylate). In some such embodiments, the UV curable resin composition further comprises ethyl(2,4,6-trimethylbenzoyl)-phenyl phosphinate, such as in a concentration of about 0.1 to 2% by weight of the curable resin composition. In some such embodiments, the UV curable resin composition further comprises a surfactant, such as e.g. 1H,1H,5H-octafluoropentyl-acrylate or a polyether-modified poly-dimethylsiloxane, as discussed below.
[0244] In embodiments, the resin composition has a surface energy below about 30 J/m.sup.2. In embodiments, the resin composition further comprises a surfactant, preferably an acrylate functionalised surfactant. A surfactant may advantageously reduce adhesion between the surface of the resin and a surface used to impart structure to the resin, such as e.g. an imprint stamp. In embodiments, the surfactant is beneficially chosen such that when the resin composition is applied on a polymeric surface such as PE or PET, the surfactant segregates more at the exposed resin surface than at the polymer-resin interface. In embodiments, the surfactant does not reduce the transparency of the cured resin composition. In embodiments, the surfactant may be used in a concentration below about 2% by weight of the curable resin composition, such as between about 0.1% and 2% by weight of the curable resin composition, or between about 0.5% and about 1% by weight of the curable resin composition, such as at most about 1% by weight of the curable resin composition. Suitable surfactants for use according to the invention include 1H,1H,2H,2H-perfluorooctyl acrylate (CAS 17527-29-6, available as Fluowet® AC600), 1H,1H,5H-octafluoropentyl-acrylate (available as Viscoat 8F from OSAKA ORGANIC CHEMICAL INDUSTRY LTD), (PFPE)-urethane acrylate (typically available in solution, such as in a solvent comprising a mixture of ethyl acetate and butyl acetate (for example 1:1 by weight), such as Fluorolink AD1700), polyether-modified poly-dimethylsiloxane (available, for example, as BYK-UV 3510), 4-(1,1,3,3-TetramethylbutyI)-phenyl-poly-ethylene glycol (available, for example, as Triton® X-100). Advantageously, surfactants for use according to the invention are not solvent-based. Particularly beneficial surfactants for use according to the invention include 1H,1H,2H,2H-perfluorooctyl acrylate (CAS 17527-29-6, available as Fluowet® AC600) and 1H,1H,5H-octafluoropentyl-acrylate (available as Viscoat 8F from OSAKA ORGANIC CHEMICAL INDUSTRY LTD). These surfactants are advantageously clear in the above-mentioned concentrations, and enable the production of a cured polymer on a support surface (such as e.g. a PET or PE surface) that shows satisfactory adhesion to the surface.
[0245] In embodiments, the composition does not comprise an anti-adhesion additive, such as a surfactant. Compositions without anti-adhesion additives may advantageously result in good adhesion between the resin when cured and a support on which the resin was cured. In particular, good adhesion properties may be advantageous when the resin is applied on a support to form a composite body when cured, and the bond between the cured resin and the support is preferably resistant to exposure to temperature changes and/or humidity. In embodiments, compositions without an anti-adhesion additive may be particularly suitable for use in combination with glass or glass-like substrates.
[0246] Table 1 below shows formulae for compounds mentioned above, that may be used as the first or second type of (meth)acrylate monomers according to the disclosure, as photoinitiators, or as surfactants, as the case may be.
TABLE-US-00001 TABLE 1 compounds for use as ingredients of UV curable resins according to the disclosure. Formula Name Use
[0247] The decorative structures according to the invention are particularly suitable for use as decorative elements for use on garments, wearables, fashion accessories, etc. where the aesthetic potential combined with the light weight, low profile and flexibility of the decorative structures of the invention are important. As such, the invention also encompasses a garment comprising a decorative structure as described. For example, the garment may be a clothing accessory such as shoes, a hat, sunglasses, glasses, bags, jewellery such as a bracelet, necklace or watch, an electronic wearable such as an activity tracker, etc. or a piece of clothing such as a shirt, jacket, jumper etc.
[0248] Other variations of the invention will be apparent to the skilled person without departing from the scope of the appended claims.
EXAMPLES
Example 1
[0249] In this example, the optical properties of a prior art crystal cut (brilliant cut as shown in
[0250]
[0251]
Example 2
[0252] In this example, the optical properties of various embodiments of the decorative structures of the invention were studied.
[0253]
[0254]
[0255]
[0256]
[0257]
[0258] Therefore, the inventors set out to investigate the relationship between the fire and the angles of the facets in a 3-fold symmetrical arrangement of grooves with two different angles of walls.
[0259]
[0260]
Example 3
[0261] In this example, the inventors investigated the optical properties of various UV curable resins according to the invention and comparative examples. The refractive indices of various cured compositions were obtained by variable angle spectroscopic ellipsometry, using a Xenon lamp between 300 and 1,700 nm and measuring at 55°, 60°, 65°, 70° and 75° angle of incidence. Abbe numbers were calculated from this data as explained above.
[0262]
[0263] The samples are as follows: sample 1: Allnex RX15331 (a nano-composite resin comprising ZrO.sub.2)+TPO-L; sample 2: M1142 +TPO-L; sample 3: M1142+SR348+TPO-L (65.3% M1142, 32,7% SR348c, 2% TPO-L, by weight); sample 4: SR348+TPO-L; sample 5: SP1106+TPO-L; sample 6: M2372+M140+TPO-L; sample 7: SC9610+TPO-L; sample 8: E207+M140+TPO-L: where M1142 is Miramer M1142 (ortho-phenyl-phenol-ethyl-acrylate, with a high refractive index but showing no crosslinking and remaining thermoplastic), SR348 is Sartomer SR348c (ethoxylated(3)bisphenol-A-dimethacrylate, with high mechanical, physical and thermal stability), SP1106 is Miramer SP1106 (a hyperbranched acrylate that shows good chemical and mechanical resistance), M2372 is Miramer M2372 (THEICTA, tris(2-hydroxyethyl)isocyanurate-tri-acrylate), M140 is Miramer M140 (2-phenoxyethyl-acrylate, with high refractive index and high flexibility), E207 is Photocryl E207 (an epoxy-acrylate that shows good adhesion to glass), and SC9610 is Miramer SC9610 (a melamine acrylate that shows high hardness and gloss, and good mechanical and chemical resistance).
[0264] The data shows that compositions with a high aromatic content according to the invention, such as samples 1, 2 and 3 have low Abbe numbers, whereas compositions that do not have high aromatic content have comparatively higher Abbe numbers. In particular, comparing samples 2, 3 and 4, it can be seen that the use of SR348 alone results in a high Abbe number, whereas use of M1142 alone, which has a higher aromatic content, results in a low Abbe number. However, the combination of M1142 and SR348 results in a formulation that has both a low Abbe number (due to the presence of M1142) and good mechanical stability due to the presence of SR348. In particular, the Abbe number of composition 3 was calculated as about 23, whereas the Abbe number of composition 4 was calculated as about 29. Amongst these, Allnex RX15331 showed a yellow coloration when cured and is as such less preferred.
[0265] Although specific embodiments have been described, it would be apparent to the skilled person that modifications and variations are possible without departing from the spirit and scope of the invention, which is defined by the appended claims. As such, the appended claims intend to cover any such embodiments. Further, it would be apparent to the skilled person that many features described in relation to particular embodiments are combinable and envisaged for combination with features described in relation to other embodiments.