Nylon Composition For Improved Sublimation

Abstract

A sublimated polymer composition with improved weatherability having a coating applied to a substrate by a sublimation process. The substrate includes about 60-90% by weight of polymer selected from the group consisting of polyamides, polyester, polyether and combinations thereof; UV absorber; UV inhibitor; pigment, and antioxidant.

Claims

1. A sublimated polymer composition comprising: a substrate comprising about 60-90% by weight of polymer selected from the group consisting of polyamides, polyester, polyether and combinations thereof; UV absorber; UV inhibitor; pigment; antioxidant; and a sublimated design applied to the substrate by a sublimation process; wherein the pigment is a compound that is different from at least one of the UV absorber and the UV inhibitor.

2. The sublimated polymer composition of claim 1, wherein the composition comprises about 0.1-10% UV absorber.

3. The sublimated polymer composition of claim 1, wherein the composition comprises about 0.1-10% UV inhibitor.

4. The sublimated polymer composition of claim 1, wherein the antioxidant is present at about 0.1-10% by weight of the composition.

5. The sublimated polymer composition of claim 1, wherein the pigment is present at about 10-30% by weight of the composition.

6. The sublimated polymer composition of claim 1, wherein the polymer consists of polyamide.

7. The sublimated polymer composition of claim 6, wherein the polyamide is selected from the group consisting of nylon 6, nylon 6,6, nylon 6,10, nylon 11, and nylon 12.

8. The sublimated polymer composition of claim 1, wherein the sublimated design is digitally printed onto the substrate.

9. The sublimated polymer composition of claim 1, wherein the sublimated design is rotogravure printed onto the substrate.

10. The sublimated polymer composition of claim 1, wherein the sublimated design is plotter printed onto the substrate.

11. The sublimated polymer composition of claim 1, wherein the sublimated composition exhibits greater resistance to weathering after 200 hours of exposure in accordance with ISO 16474-2:2013.

12. The sublimated polymer composition of claim 1, wherein the sublimated composition exhibits greater resistance to weathering after 600 hours of exposure in accordance with ISO 16474-2:2013.

13. A pellet prepared from the composition of claim 1.

14. A melt-extruded product prepared from the composition of claim 1.

15. A sublimated polymer composition for improved sublimation comprising a substrate comprising about 60-90% by weight of at least one polyamide selected from the group consisting of nylon 6, nylon 6,6, nylon 6,10, nylon 11, nylon 12 and combinations thereof; about 0.1-10% organic UV absorber; about 0.1-10% organic UV inhibitor; about 10 to 30% pigment; about 0.1 to 10% by weight antioxidant; and a sublimated design applied to the substrate by a sublimation process.

16. The sublimated polymer composition of claim 15, wherein the polyamide consists essentially of nylon 6,6.

17. The sublimated polymer composition of claim 15, wherein the UV absorber is selected from the group consisting of hindered amine light stabilizers, hydroxybenzophenones, hydroxybenzotriazoles, hydroxybenzotriazines, cyanoacrylates, oxanilides, benzoxazinones, benzotriazoles, triazines, and combinations thereof.

18. The sublimated polymer composition of claim 15, wherein the UV inhibitor comprises one or more benzotriazoles.

19. The sublimated polymer composition of claim 15, wherein the pigment is a non-white pigment.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0029] FIG. 1 is a sublimated polymer article in accordance with the invention.

[0030] FIG. 2 shows comparative results of product produced in accordance with and without the invention after exposure to an accelerated weathering test.

[0031] FIG. 3 shows comparative results of product produced in accordance with and without the invention after exposure to an accelerated weathering test.

[0032] The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.

DETAILED DESCRIPTION OF THE INVENTION

[0033] Sublimated polymer-based products prepared from polyamide, polyester or polyether polymer compositions containing UV absorber show improvement in weatherability. The inventor has found that compositions comprising about 60-90% by weight of polymer selected from the group consisting of polyamides, polyester, polyether and combinations thereof; UV absorber; UV inhibitor; pigment, and antioxidant, which may be formed into plastic pellets or other products for sublimation, have increased resistance to weathering compared to prior polymer compositions.

[0034] FIG. 1 shows a sublimated plastic automatic gear of a car 10 in accordance with the invention. The gear 10 comprises a polymer-based substrate 2 to which a patterned design 4 has been applied by a sublimation printing process. The substrate 2 is comprised of thermoplastic polymer, UV absorber, UV inhibitor, pigment, and antioxidant.

[0035] Polymer:

[0036] The term, polymer refers to, but is not limited to, oligomers, homopolymers, copolymers, terpolymers, and the like.

[0037] The polymer may be thermoplastic. In one embodiment the thermoplastic polymer may be a melt-processable polymer which may be employed together with the UV absorbers, UV inhibitors, pigments and antioxidants of this disclosure. Typically the polymer is a high molecular weight polymer and is thermoplastic. High molecular weight is meant to describe polymers having a melt index value of about 0.01 to about 50, typically from about 2 to about 10 as measured by ASTM method D1238-98. By melt-processable, it is meant a polymer that can be extruded, molded, laminated or otherwise converted into shaped articles through a stage that involves obtaining the polymer in a molten state.

[0038] The polymer must be able to withstand temperatures above 170-180 C., typically greater than 200 C., in a sublimation process, or adaptable to withstand such temperatures by incorporation with additional ingredients.

[0039] In another embodiment, the polymer is thermosetting. Thermosetting resins are those which change irreversibly due to heat or or catalyst from a fusible and or soluble material into one which is infusible and insoluble through the formation of a covalently cross linked, thermally stable network. Typical thermosetting resins include epoxy, phenolic, amino, unsaturated polyester and urethanes.

[0040] Polymers which are preferred for use in this disclosure include, by way of example but not limited thereto, are polymers of the polyamide family, polyester family and polyether family.

[0041] In general, polyamides refer to high molecular weight polymers in which amide linkages (CONH) occur along the length of the molecular chain. Suitable polyamides for use in the compositions of this invention may be obtained, for example, by: (1) polycondensation of (a) a dicarboxylic acid, such as oxalic acid, adipic acid, sebacic acid, terephthalic acid, isophthalic acid or 1,4-cyclohexanedicarboxylic acid, with (b) a diamine, such as ethylenediamine, tetramethylenediamine, pentamethylenediamine, hexamethylenediamine, or decamethylenediamine, 1,4-cyclohexyldiamine or m-xylylenediamine; (2) a ring-opening polymerization of cyclic lactam, such as -caprolactam or -laurolactam; (3) polycondensation of an aminocarboxylic acid, such as 6-aminocaproic acid, 9-aminononanoic acid, 11-aminoundecanoic acid or 12-aminododecanoic acid; or (4) copolymerization of a cyclic lactam with a dicarboxylic acid and a diamine.

[0042] The polymers may have various structures including, but not limited to, regular, irregular, alternating, periodic, random, block, graft, linear, branched, isotactic, syndiotactic, atactic, and the like.

[0043] Polyamide polymers include, but are not limited to, polyamide copolymers (copolyamides) having two types of monomers, copolymers having three types of monomers, and copolymers having more than three types of monomers. Blends and alloys of polyamides also may be made in accordance with this invention as described further below. Specific examples of suitable polyamides include, but are not limited to, nylon 6, nylon 6,6; nylon 6,10; nylon 11, and nylon 12. Aliphatic and aromatic polyamides and blends thereof may be prepared in accordance with this invention. In certain preferred embodiments, the polyamide may be nylon 6,6. Different commercially-available nylon resins may be used in accordance with the present invention including, but not limited to polyammide 6.6 resins available from Ascend Performance Materials and LG Chem LTD, Plastamid, Trimid and Polyram nylon 6,6 and nylon 6 resins, available from Polymer Technology & Services, LLC; Technyl nylon 6,6 and nylon 6 resins, available from Rhodia Engineering Plastics; Ultramid and Capron nylon 6 resins, available from BASF; Cristamid and Rilsan nylon resins, available from Arkema Inc; Vestamid nylon resins, available from Evonik Industries; Zytel and Elvamide nylon resins, available from the DuPont Company; and Grivory GTR 45 and Grilamid TR-90, transparent nylon resins, available from Grilamid EMS.

[0044] Another example of a group of suitable polyamides is thermoplastic polyamide elastomers. Thermoplastic polyamide elastomers typically are copolymers of a polyamide and polyester or polyether. For example, the thermoplastic polyamide elastomer can contain a polyamide (for example, nylon 6, nylon 6,6; nylon 11, nylon 12 and the like) as a hard segment and a polyether or polyester as a soft segment.

[0045] Polyesters refers to polymers that contain a plurality of ester linkages. The most commonly used polyester is polyethylene terephthalate (PET). Other commonly used polyesters include polybutylene terephthalate (PBT), polybutylene succinate (PBS), polyethylene adipate (PEA), polycaprolactone (PCL), and polylactic acid (PLA). Different commercially-available polyester resins may be used in accordance with the present invention.

[0046] Polyethers refers to a group of compounds containing a comprehensive monol having an ether bond, and polyols and derivatives thereof. Different commercially-available polyether resins may be used in accordance with the present invention.

[0047] In particular embodiments, the polymer may be selected from the group consisting of Polyammide 66=PA 66, Polyammide 6=PA 6, Polyammide 6 10=PA 610, Polyammide 11=PA 11 and Polyammide 12=PA 12. Alternatively, the polymer may be selected from the group consisting of Polybutilentereftalato=PBT and Polyetilentereftalato=PET. In certain embodiments, the polymer may be selected from the group consisting of Polyetersolfone=PSO, Polysulfone=PSU and Polyfenil oxide=PPO. Mixtures of polymers are also contemplated.

[0048] Different rheological modifiers may be included in the polymer at about 10% to about 30% by weight, more preferably 15% to 25% by weight, most preferably at around 20% by weight. As one non limiting example polyamide 6 may be used to modify polyamide 6,6 polymer.

[0049] The polymer is present in the amount of about 60% to 99% by weight, more preferably about 60% to about 90% by weight of the composition, based on the total weight of solids. In some embodiments, the polymer is present in the amount of about 80%20. Most preferably, the polymer is present in the amount of about 80%.

[0050] Pigment:

[0051] Any conventional colorant such as a pigment, dye or a dispersed dye may be used in this disclosure to impart color to the polymer-based product wherein the pigment is resistant to temperatures greater than or equal to 170 C. In one embodiment, generally, about 0.1% to about 30% by weight of conventional pigments, based on the total weight of the component solids, can be added. More typically, about 10% to about 30% by weight of conventional pigments, based on the total weight of component solids, can be added. Most typically, about 20% by weight of conventional pigments, based on the total weight of component solids, can be added. Conventional compounding techniques such as Banbury, twin screw, or continuous mixer may be used to disperse the pigments to form a compound or concentrate. The compound or concentrate may then be blended with additional constituents of the polymer-based product in order to form the final product.

[0052] The pigment component of this disclosure may be any of the generally well-known pigments or mixtures thereof used in polymer-based products wherein the pigment is resistant to temperatures greater than or equal to 170 C. Some suitable examples may be found in Chapter IV, Volume I Powder Coatings, The Technology, Formulation and Application of Powder Coatings by David M Howell (2000), Special Effect Pigments by Gerhard Pfaff (2008), and Metallic Effect Pigments by Peter Wissling (2006). Any of the commercial pigments used in polymer-based products can be utilized in these compositions such as the following: metallic oxides, such as titanium dioxide, zinc oxide, aluminum oxide, and iron oxide, metal hydroxide, metal flakes, such as aluminum flake, chromates, such as lead chromate, sulfides, sulfates, carbonates, carbon black, silica, talc, china clay, phthalocyanine blues and greens, organo reds, organo maroons, pearlescent pigments and other organic pigments and dyes. If desired chromate-free pigments, such as barium metaborate, zinc phosphate, aluminum triphosphate and mixtures thereof, can also be used.

[0053] Some useful pigments include C.I. Pigments: Black 12, Black 26, Black 28, Black 30, Blue 15.0, Blue 15.3 (G), Blue 15.3 (R), Blue 28, Blue 36, Blue 385, Brown 24, Brown 29, Brown 33, Brown 10P850, Green 7 (Y), Green 7 (B), Green 17, Green 26, Green 50, Violet 14, Violet 16, Yellow 1, Yellow 3, Yellow 12, Yellow 13, Yellow 14, Yellow 17, Yellow 62, Yellow 74, Yellow 83, Yellow 164, Yellow 53, Red 2, Red 3 (Y), Red 3 (B), Red 4, Red 48.1, Red 48.2, Red 48.3, Red 48.4, Red 52.2, Red 49.1, Red 53.1, Red 57.1 (Y), Red 57.1 (B), Red 112, Red 146, Red 170 (FSRK Type) Bluer, C.I. Pigment Orange 5, Pigment Orange 13, Pigment Orange 34, Pigment Orange 23 (R), and Pigment Orange 23 (B). Some useful organic pigments include: Pigment Yellow 151, Pigment Yellow 154, Pigment Yellow 155, Pigment Red 8, Pigment Red 8, Pigment Red 49.2, Pigment Red 81, Pigment Red 169, Pigment Blue 1, Pigment Violet 1, Pigment Violet 3, Pigment Violet 27, Pigment Red 122, Pigment Violet 19. Some useful inorganic pigments include: Middle Chrome, Lemon Chrome, Prime-Rose Chrome, Scarlet Chrome, and Zinc Chromate.

[0054] More typical pigments include: Black 12, Black 26, Black 28, Black 30, Blue 28, Blue 36, Blue 385, Brown 24, Brown 29, Brown 33, Green 17, Green 26, Green 50, Violet 14, Violet 16, Yellow 164 and Yellow 53.

[0055] Suitable preferred pigments may be commercially obtained from BASF, Clarian and Allnex.

[0056] UV Inhibitor:

[0057] Suitable UV inhibitors include, for example, benzotriazoles such as 2-(2-hydroxy-5-methylphenyl)benzotriazole, 2-(2-hydroxy-5-tert-octylphenyl)-benzotriazole and 2-hydroxy-4-n-octoxy benzophenone or the like or combinations including at least one of the foregoing light stabilizers.

[0058] These types of ingredients may also be obtained from BASF, Clarian and Allnex.

[0059] UV inhibitors are generally used in amounts of 0.1 wt. % to 10.0 wt. %, or about [insert narrower range] wt. %, of the polymer composition, but could be used in other amounts.

[0060] UV Absorber:

[0061] Suitable UV absorbers include conventionally disclosed UV absorbers, for example, hydroxybenzophenones; hydroxybenzotriazoles; hydroxybenzotriazines; cyanoacrylates; oxanilides; benzoxazinones; 2-(2H-benzotriazol-2-yl)-4-(I,I,3,3-tetramethylbutyl)-phenol (CYASORBT 5411); 2-hydroxy-4-n-octyloxybenzophenone (CYASORB 531); 2-[4,6-bis(2,4-dimethylphenyl)-I,3,5-triazin-2-yl]-5-(octyloxy)-phenol (CYASORB 1164); 2,2-(I,4-phenylene)bis(4H-3,I-benzoxazin-4-one) (CYASORB UV-3638); I,3-bis[(2-cyano-3,3-diphenylacryloyl)oxy]-2,2-bis[[(2-cyano-3,3-diphenylacryloyl)oxy]methyl]propane (UVINUL 3030); 2,2-(I,4-phenylene)bis(4H-3,I-benzoxazin-4-one); 1,3-bis[(2-cyano-3,3-diphenylacryloyl)oxy]-2,2-bis[[(2-cyano-3,3-diphenylacryloyl)oxy]methyl]propane; nano-size inorganic materials such as titanium oxide, cerium oxide, and zinc oxide, all with particle size less than 100 nanometers.

[0062] Suitable UV absorbers further includes hindered amine light stabilizers (HALS) or the like, or combinations including at least one of the foregoing conventional UV absorbers. Blends of HALS with other UV absorbers that may be suitable are available from BASF under the Tinuvin product line. Preferable UV absorbers may also be commercially obtained from Clarian and Allnex.

[0063] In some embodiments, the UV absorber is preferably a second generation absorber. In certain preferred embodiments the UV absorber is selected from one or more of benzotriazole, HALS, triazine and hydro phenyltriazine.

[0064] UV absorbers have been described in Powder Coatings Chemistry and Technology by Pieter Gillis de Lange (a photocopy of a relevant page is included with the IDS), which is incorporated herein by reference in its entirety.

[0065] UV absorbers are generally included in amounts of 0.1 wt. % to 10.0 wt. %, or about 0.5% to about 7.5% of the composition, more preferably about 2.0% to about 5.0% of composition.

[0066] Antioxidants:

[0067] Suitable antioxidants are conventionally known in the polymer arts and include, for example, organophosphites such as tris(nonyl phenyl)phosphite, tris(2,4-di-t-butylphenyl)phosphite, bis(2,4-di-t-butylphenyl)pentaerythritol diphosphite, distearyl pentaerythritol diphosphite or the like; alkylated monophenols or polyphenols; alkylated reaction products of polyphenols with dienes, such as tetrakis[methylene(3,5-di-tert-butyl-4-hydroxyhydrocinnamate)]methane, or the like; butylated reaction products of para-cresol or dicyclopentadiene; alkylated hydroquinones; hydroxylated thiodiphenyl ethers; alkylidene-bisphenols; benzyl compounds; esters of beta-(3,5-di-tert-butyl-4-hydroxyphenyl)-propionic acid with monohydric or polyhydric alcohols; esters of beta-(5-tert-butyl-4-hydroxy-3-methylphenyl)-propionic acid with monohydric or polyhydric alcohols; esters of thioalkyl or thioaryl compounds such as distearylthiopropionate, dilaurylthiopropionate, ditridecylthiodipropionate, octadecyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, pentaerythrityl-tetrakis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate or the like; amides of beta-(3,5-di-tert-butyl-4-hydroxyphenyl)-propionic acid or the like, or combinations including at least one of the foregoing antioxidants.

[0068] Antioxidants preferably may also be obtained from BASF, Clarian and Allnex.

[0069] Antioxidants are generally used in amounts of 0.1 wt. % to 10 wt. %, or about 1.0 to about 7.0 wt. %, of the resin composite, but could be used in other amounts. Most preferably, antioxidant is present at about 3 wt. %.

[0070] Other Components:

[0071] Optionally, the polymer blends disclosed herein can comprise at least one additive for the purposes of improving and/or controlling the processibility, appearance, physical, chemical, and/or mechanical properties of the polymer blends. In some embodiments, the polymer blends do not comprise an additive. Any plastics additive known to a person of ordinary skill in the art may be used in the polymer blends disclosed herein. Non-limiting examples of suitable additives include slip agents, anti-blocking agents, plasticizers, fillers, lubricants, antifogging agents, flow aids, coupling agents, cross-linking agents, nucleating agents, surfactants, solvents, flame retardants, antistatic agents, oil or extender, odor absorber and combinations thereof.

[0072] Other components may be present in the polymer composition at 0-5% by weight.

[0073] Functional additives may be included in the compositions at 0-60%, more preferably 10-50%, most preferably 20-40% by weight. Non-limiting examples include antimicrobial additives, additives to lower the electrical resistance in order to improve conductability, pigments that can change colors with temperature and with different electrical tension applied and glow in the dark additive.

[0074] Preparation of Polymer Pellets

[0075] The present disclosure provides a process for preparing a polymer-based product from a powder-containing polymer composition. Typically, in this process, the composition components are weighed in the lab and mixed in a suitable container. The container is installed on a mixer to obtain perfect mixing of all components. The material is extruded so that it has a homogeneous mixture and the extruded materials are cooled. Subsequently, the cooled material is broken into pellets in a shape and size that is ideal for future use.

[0076] In one embodiment, pigment, UV inhibitor and UV absorber, and antioxidant may be contacted with a melt processable polymer. Any melt compounding techniques, known to those skilled in the art may be used. Any means of combining or blending the ingredients known to those skilled in the art may be used. Processing temperatures depend on the polymer and the blending method used, and these are well known to those skilled in the art. The intensity of mixing depends on the polymer characteristics.

[0077] The resulting polymer compositions of this disclosure are useful in production of shaped substrates. The amount of polymer, pigment, UV absorber, UV inhibitor, antioxidant and additional components present in this polymer composition and shaped polymer-based product will vary depending on the end use application.

[0078] It is preferable that the compositions are able to withstand high temperatures necessary for sublimation and pressures of 30-90 psi.

[0079] Substrates:

[0080] The polymer compositions and pellets may be used to form various substrates suitable for sublimation.

[0081] In one embodiment, a polymer-based product or shaped article such as a plastic part is typically produced by feeding an injection molding machine with pellets of the invention, and adjusting the setting of the machine as per technical data sheets of the pellets. The pellets are fused inside an injection syringe and then injected in a mold. The space of the mold is filled with the pellets and then immediately cooled down so the piece can exit the mold.

[0082] This disclosure is particularly suitable for producing articles such as windows, doors, garage doors, railing, fencing, decking, shutters, louvers, awning, thresholds, furniture for office, and patio, cabinets, bar table-chairs, lockers, doors, shelves, racks, display cabinets, signage, stanchions, trash cans, and components of bicycles, motorcycles, cars, etc.

[0083] The shaped articles are suitable for sublimation printing processes. Sublimation printing may be carried out using typical conditions/equipments used in the art. Preferably, a coating is digitally printed, rotogravure printed or plotter printed onto the polymer-based substrate.

[0084] Coating:

[0085] The coating applied to the substrate may include decorative powder coatings, transfer films and inks. Powder coatings includes polyesters, polyurethanes and epoxy. Transfer films includes film to paper or pet. Inks that may be applied in the coating include sublimation inks.

[0086] Decoral System provides turn-key sublimation equipment to OEMs, extruders, and powder coating facilities throughout the world. Products are initially powder coated (or liquid painted). A transfer film, printed with special inks, is applied over the products under vacuum for a tight contact. Products are then loaded into a decoration machine at high temperature that turns inks into a gas that penetrates deep into the coated layer. Products are then taken out of the decoration machine and the used films are peeled off to reveal the images. At this point the products are completely decorated and ready for shipment. No additional protection coatings are required.

[0087] The coating may take the form of various patterns. For instance a wide range of wood grain, marble, granite and fantasy patterns may be applied during the sublimation printing.

[0088] The sublimated substrates are advantageously Anti-Graffiti, Anti-Slip, Anti-Microbial, Anti-Scratch, Super-Durable (UV resistant) and TGIC free (non-toxic).

[0089] Accelerated weathering tests including ISO 16474-2:2013, ASTM D2565, ASTM D4459, ASTM DG155, ISO 4892, and SAE J1885 use Xenon arc exposure to assess how a plastic will perform outdoors. Although these tests provide useful information, they do not precisely predict with how long a plastic part will last in an outdoor environment. A typical guideline is that it takes 1500 hours of xenon arc exposure to achieve the same amount of radiation as 12 months of outdoor use in Florida.

[0090] Sublimated articles produced in accordance with the invention exhibit greater resistance to weathering after 200 and 600 hours of exposure in accordance with ISO 16474-2:2013 than product that does not employ the inventive polymer compositions and are expected to produce superior results when subjected to alternative weathering tests. The content of ISO 16474-2:2013 is incorporated herein by reference.

[0091] The examples which follow are not intended to limit the scope of the disclosure. Various modifications, alternative constructions and equivalents may be employed without departing from the true spirit and scope of the invention.

EXAMPLES

Example 1

Formulation of Sublimation Polymer

[0092]

TABLE-US-00001 FORMULATION SUBLIMATION POLYMER Description of components Quantity Range Nylon polymer 80 20 Rheologic Polymer Modifier 20 10 Various Functional Additives 30 30 Phenolic base 1.5 1 Phosfit/diphosfit base (Antioxidant) 1.5 1 UV absorber 1 1.8 1 UV absorber 2 1.8 1 UV absorber 3 0.5 0.3 UV absorber 4 0.5 0.3 Other various pigments resistant t >250 C. 20 10

Example 2

Comparative Study

[0093] Objective: Study and evaluation of Decoral System plastic polymer.

[0094] Sample Specification:

TABLE-US-00002 ID Type of Sample Sublimation Film Exposure Time 1 w/o UV absorber 6007/01 600 hours 2 With UV absorber 6007/01 600 hours 3 w/o UV absorber Film by Plotter 200 hours 4 With UV absorber Film by Plotter 200 hours

[0095] Testing Machine: Qsun 3000, Reference method: ISO 16474-2 with a dry cycle of 102 minutes and a wet cycle of 18 minutes (550 W/m2 290-800 nm) until the end of the test. Visual evaluation was conducted before and after test due to unusual shape of the samples.

[0096] Results: FIG. 2 shows results of sample ID 1 on left and sample ID 2 on right. Exposed sample is shown on the top and reference samples are shown on the bottom. FIG. 3 shows results of sample ID 4 on the left and sample ID 3 on the right. Reference product is shown on top and exposed sample is shown on the bottom.

[0097] Observations: the Decoral System plastic polymer, with and without UV absorber, can receive sublimation ink from rotogravure printing (6007/01 film) and also from plotter printing; if UV absorber is used, improved resistance of sample and protection of the sublimation ink was observed. It is understood that the UV absorber may also be referred to as a UV inhibitor.

[0098] It is understood that the compositions and products described and illustrated herein represent only some embodiments of the invention. It is appreciated by those skilled in the art that various changes and additions can be made to compositions and products without departing from the spirit and scope of this invention. It is intended that all such embodiments be covered by the appended claims.