US20090317649A1 - Multilayer Clear Over Color Polyolefin Sheets and Layered Backing Structure - Google Patents

Abstract

A multilayer structure includes a clear polyolefin layer, a colored polyolefin layer, and a random polyolefin backing layer. The colored and backing layers are coextruded and are permanently bonded at a layer interface, which is exclusive of an adhesive. The structure has a DOI of 70 or greater and passes a gravelometer impact test per the GM9508P standard, with a 10 pint load, at a −30° C. temperature, and at an impact angle of 30 degrees. Among other uses, the structures are appropriate for use as body panels in the motor vehicle industry. The structures display a “class A” finish and meet a variety of requirements for durability and weatherability. An ABA structured backing layer and a method of making it are also described herein.

Description

CROSS REFERENCE TO RELATED APPLICATION
• This application is a continuation of PCT application No. PCT/US09/42704, which was filed on May 4, 2009, which in turn claimed the benefit of priority from U.S. Provisional Application No. 61/050,465, filed on May 5, 2008. These prior applications, including the written description and drawing figures, are hereby incorporated into the present application by reference.
BACKGROUND
• Many different types of articles produced today are formed from coextruded or laminated sheets. For the composition of these sheets there are several different types of competing technologies, such as painted plastic, solvent cast fluoro-acrylic film, coextruded ionomer decorative sheet, painted metal, & coextruded acrylic/ABS sheet.
• For many polymeric articles of manufacture, optical and durability characteristics are very important. Particularly in the transportation industry, the qualities of distinction of image, gloss, imprint resistance, scratch resistance, mar resistance, and corrosion resistance are highly desirable among other measures of durability and optical quality. Achieving a balance of excellent optical qualities and excellent durability qualities is a difficult endeavor and is complicated by the unpredictability of chemical interactions between various materials used in such compositions. It is particularly difficult to achieve an excellent balance of properties in a final formed product that has been subjected to heat and/or elongation.
• In addition, sheet formed thermoplastic polyolefin (TPO) typically includes a mixture of both virgin polymer and regrind polymer. TPO is a blend of an olefin, an elastomer, and a filler such as talc. The addition of regrind polymer is considered a necessary practice within the sheet extrusion industry in order to control costs by minimizing waste and reducing the overall raw material cost of the final part. Although the economics improve with the addition of regrind, the added regrind contributes to a lower melt strength and the sag resistance of the sheet is significantly reduced. A low sag resistance can cause defects such as excessive “webbing” in tight corners, surface tears in areas of high stretch, and non-uniform wall thickness. Significant variation in wall thickness throughout a part can cause excessive warping and/or deterioration of physical properties.
SUMMARY
• This application describes novel multilayer structures that include a clear polyolefin layer, a colored polyolefin layer, and a random polyolefin backing layer. The colored and backing layers are coextruded and are permanently bonded at a layer interface. In another embodiment, the clear polyolefin layer is also coextruded and permanently bonded over the colored backing layer. These structures have a DOI of 70 or greater and pass a gravelometer impact test per the GM9508P standard, with a 10 pint load, at a −30° C. temperature, and at an impact angle of 30 degrees. The multilayer structures retain DOI and gravelometer impact standards as stated above even after being subjected to heat and/or elongation to make a final formed product. Among other uses, the structures are appropriate for use as vehicle body panels.
• A formed product is described that includes a coextruded clear isotactic polypropylene/ethylene copolymer layer of 1 mil to 20 mils in thickness, alternatively 2.5 mils to 20 mils in thickness; a coextruded colored isotactic polypropylene/ethylene copolymer layer of 3 mils to 20 mils in thickness, alternatively 1 mil to 20 mils in thickness; and a polyolefin backing layer with a random microstructure. The clear and color layers are coextruded and are permanently bonded at a layer interface. The formed product has a DOI of 70 or greater. The formed product is substantially non-oriented by stretching. The formed product has a gloss of 75 or greater at a 60° angle and a gloss of 60 or greater at a 20° angle. The clear polyolefin layer has a light transmittance of 90% or greater. The clear polyolefin layer has a haze of 10 or less. The formed product exhibits no gauze imprint at 70° C. minimum under a 500 g load applied over a 40 mm diameter for two hours. The formed product passes a gravelometer impact test per the GM9508 standard, with a 10 pint load, at a −30° C. temperature, and at an impact angle of 30 degrees.
• A vehicle body panel is described herein that includes a multilayer structure. The multilayer structure includes a coextruded clear isotactic polypropylene/ethylene copolymer layer of 1 mil to 20 mils in thickness, alternatively 2.5 mils to 20 mils in thickness; a coextruded colored isotactic polypropylene/ethylene polyolefin layer of 1 mils to 20 mils thick, alternatively 3 mils to 20 mils in thickness; and a polyolefin backing layer with a random microstructure. The clear and color layers are coextruded and are permanently bonded at a layer interface. The structure has a DOI of 70 or greater. The structure is substantially non-oriented by stretching. The structure has a gloss of 75 or greater at a 60° angle and a gloss of 60 or greater at a 20° angle. The clear polyolefin layer has a light transmittance of 90% or greater. The clear polyolefin layer has a haze of 10 or less. The structure exhibits no gauze imprint at 70° C. minimum under a 500 g load applied over a 40 mm diameter for two hours. The structure passes a gravelometer impact test per the GM9508 standard, with a 10 pint load, at a −30° C. temperature, and at an impact angle of 30 degrees. Furthermore, the clear and/or color layers include an additive selected from the group consisting of: antioxidants, UV stabilizers, slip agents, and combinations of these.
• In another embodiment, a multilayer structure includes a clear polyolefin layer, and a colored polyolefin backing layer with a random microstructure. The clear and backing layers are coextruded and are permanently bonded at a layer interface. The interface is exclusive of an adhesive layer, and the structure has a DOI of 70 or greater. In addition, the structure passes a gravelometer impact test per the GM9508P standard, with a 10 pt load, at a −30° C. temperature, and at an angle of 30 degrees.
• A method of forming the above structures is also described.
• This application further describes a multilayer structure that includes a first thermoplastic layer having a polymeric component consisting essentially of virgin polyolefin, a second thermoplastic layer including regrind polyolefin, and an optional third thermoplastic layer having a polymeric component consisting essentially of virgin polyolefin. The second thermoplastic layer is adjacent to the first thermoplastic layer and the third thermoplastic layer, if present.
• A method for forming a multilayered polymeric structure is also described. The method includes: coextruding a first thermoplastic layer having a polymeric component that consists essentially of a virgin polyolefin with a second thermoplastic layer that includes regrind polyolefin, and optionally with a third thermoplastic layer having a polymeric component that consists essentially of a virgin polyolefin. The second thermoplastic layer is adjacent to the first thermoplastic layer and the third thermoplastic layer, if present.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a cross-sectional view of an example coextruded three-layer film.
• FIG. 2 is a cross-sectional view of an example three-layer film for lamination.
• FIG. 3 is a cross-sectional view of an example coextruded four-layer film.
• FIG. 4 is a cross-sectional view of an example four-layer film for lamination.
• FIG. 5 is a cross-sectional view of an example coextruded two-layer film.
• FIG. 6 is a cross-sectional view of an example vehicle body panel.
• FIG. 7 is a cross-sectional view of a second example vehicle body panel.
• FIG. 8 is a cross-sectional view of an example multi-layer structure with an ABA backing layer.
• FIG. 9 is a cross-sectional view of an example multi-layer structure with an AB backing layer.
• FIG. 10 is a cross-sectional view of a mono-layer virgin/regrind blended backing layer and an ABA backing layer.
• FIG. 11 is a graph comparing the “bag time” of a mono-layer virgin/regrind blended backing layer and an ABA backing layer.
DETAILED DESCRIPTION
• The example multilayer structures disclosed herein provide a paint-free plastic sheet structure that may be designed to simulate the appearance of painted metal or plastic. Example multilayer structures include a clear polyolefin layer over a colored polyolefin layer. Another example is a multilayer structure with a clear polyolefin layer over a translucent polyolefin layer, over a color polyolefin layer. For each of these examples the multi-layer structures are provided with a thermoplastic polyolefin backing layer. Yet another example includes a clear polyolefin layer over a colored backing layer. Preferably, there is no adhesive layer at the interface between the clear layer and the color layer and there is no adhesive layer at the interface between the layer attached to the backing layer. Most preferably, the interface between all layers of the multilayer structures is free of all adhesives. An additional disposable mask layer may be provided on each of the example structures. Furthermore, in some examples, more than one color layer, more than one clear layer, and/or more than one backing layer may be employed.
• The example multilayer structures may be formed into an article or laminated onto a substrate to produce an article. Example articles include a vehicle body panel, bumper fascia, and rocker panel.
• In the field of polymeric multilayer sheets, compositional design changes that result in improvements in one or more optical or material characteristics typically result in a deterioration in another optical or material characteristic. For example, modifying a product to make it more durable will likely result in a deterioration in optical qualities. This is partly due to the unpredictable nature of the chemical interactions, differences in refractive indexes of the blended components, and component compatibilities. This makes it quite difficult to achieve a balance of excellent properties across several categories of optical and durability characteristics.
• The example multilayer structures display an excellent balance of properties. Improvements in durability and weatherability were realized without sacrificing the appearance requirements needed (DOI—70 min, 85 min preferred; Gloss—75 min @ 60 degrees, 60 min @ 20 degrees) in order to achieve a “Class A” finish on parts of 0% stretch or greater. These improvements enable the multi-layer structures to be used by auto manufacturers and others as vehicle panels, bumper fascias, and/or rocker panels, among other uses.
• In the example multilayer structures, a combination of several design elements produces the desired balance of excellent properties. An efficient, reduced-layer structure is employed that does not require an adhesive to bond the layers of the structure together. Like chemistries in the bonded layers allows the layers to bond to each other at the layer interface. Coextrusion technology promotes the bonding of layers and provides a smooth finish. Appropriate selection of polyolefins, additives, and pigmentation for each layer also contributes to the balance of properties. In addition, further processing techniques and additives are also used to optimize the optical and durability characteristics of the multilayer structures.
• The clear layer, the color layer, and the backing layer of the example multilayer structures are permanently bonded by using like chemistries. Like chemistries in this application means belonging to same family of olefinic hydrocarbons. Each layer is coextruded from a like olefinic material. This results in permanent bonding at each layer interface between the like olefinic materials. By eliminating the adhesive at the interface, the durability of the multilayer structures is improved. As mentioned above, the bond at each layer interface is permanent which results in a product that does not delaminate when exposed to heat, sunlight, extreme cold, humidity, water immersion, chemicals, and gravel impact. In contrast, if there were a coextruded adhesive layer interposed between the layers it would create a structure that inherently has a “weak link” that could fail and result in delamination. In addition, the example multilayer structures have a ΔL of 2 or less, according to the GM9302P stress whitening resistance standard. An added benefit to the adhesive-layer-free structures is that the sheet product becomes less complex to manufacture.
• The clear layer, the color layer, and the backing layer of the multilayer structures are primarily composed of an olefinic material. For example, polypropylene/ethylene copolymer may be used as the olefinic material for each layer.
• FIGS. 1 and 2 both show example three-layer coextruded olefinic sheet structures.
• FIG. 1 illustrates anexample sheet structure1 that can be used to make both thick and thin sheets. A multilayer structure as thin as 3 mils to as thick as 540 mils may be created according to thissheet structure1. Multilayer structures of intermediate thicknesses may also be created, for example, 8.5 mils to 540 mil, 20 mils to 450 mil, 50 mils to 300 mil, or 150 mils to 250 mils. Relatively thick sheets may be used in applications where it is desired to thermoform a part directly from the sheet itself, or thinner sheets may be desirable to thermoform a shell that is suitable to be backfilled via injection molding to achieve the final thickness. Other processes that can be used with this type of sheet/film structure include compression molding and simultaneous in-mold thermoforming/injection backfill processes.
• Theclear layer3 is 1 to 20 mils in thickness, for example, 2.5 to 20 mils, 3.0 to 15 mils, or 5.0 to 10 mils. It is primarily made of a polyolefin, such as a polypropylene/ethylene copolymer. An example polypropylene/ethylene copolymer for use in theclear layer3 has a monomer ratio of 0.5-12% ethylene, such as 1-7%, 2-10%, or 3-7% ethylene. The example polypropylene/ethylene copolymer may be isotactic, such as greater 70%, greater 80%, or greater than 90% isotactic and have a random microstructure. The crystallinity of the example polypropylene/ethylene copolymer may be greater than 60%, such as greater than 70%, or greater than 90%. The example copolymer may have a Rockwell hardness of R80 or greater, such as R100 or greater, or R105 or greater. The melting point of the example copolymer is greater than 155° C., such as, 156° C. to 300° C., 156° C. to 170° C., or 156° C. to 165° C. The example polypropylene/ethylene copolymer may have a flexural modulus of greater than 1850 MPa, such as 1900 to 2500 MPa, or 2000 to 2100 MPa. A blend of polyolefins may also be employed in theclear layer3; for example, a blend of majority isotactic polyolefin and a minority of syndiotactic polyolefin or atactic polyolefin. Example isotactic polyolefins include those sold under the following trade names: INSPIRE 404 polypropylene (Dow), CLYRELL RC514 L (LyondellBasell), INSPIRE 117 polypropylene (Dow), SR257M (LyondellBasell), 6289MZ (Total), 6D83K (Dow), and PRISMA 3410 polypropylene (Braskem). Example syndiotactic polyolefins include those sold under the following trade names: TOTAL Polypropylene 1251 (2 MI, 6.9% Haze, 130° C. melt point) and TOTAL polypropylene 1471 (4 MI, 4.8% Haze, 130° C. melt point). Another example polyolefin is NOTIO from Mitsui Chemicals (Haze 4-7%,Melt point 100° C.-135° C.). An example atactic polypropylene is FF018F from Sunoco (1.8 Melt Flow g/10 min at 230 C with 2.16 kg weight). A metallocene-based copolymer or homopolymer of propylene may also be used. INSPIRE 404, for example, is a highly isotactic, highly crystalline polypropylene/ethylene copolymer containing about 1-7% ethylene monomer. It has a flexural modulus of 2070 MPa (⅛ inch bar), a melting point of 156° C., an enthalpy of melting of 96 J/g, and a Rockwell hardness of R105 hardness. Additives, such as UV stabilizer, e.g. CYASORB THT 7001 (Cytec Industries), Antioxidants, e.g. HOSTANOX PEP-Q (Clariant), and slip agents, e.g. CRODAMIDE ER (Croda), may also be added to the polyolefin.
• Theclear layer3 should have a light transmittance of 85-100%, such as 88-100%, or 90-100%. It should also have a haze of no greater than 10%, such as no greater than 8%, no greater than 5%, no greater than 2.5%, or no greater than 1.0%. For certain applications it may be desirable to include a small amount of pigment or special effects in theclear layer3.
• Thecolor layer5 is 1 to 20 mils in thickness, for example 3.0 to 20 mils, 4.0 to 15 mils, or 5.0 to 10 mils. Thecolor layer5 is primarily made of a polyolefin, such as polypropylene/ethylene copolymer. Preferably, theclear layer3 and thecolor layer5 will have like chemistries, that is, they will be of the same type of polyolefin and similar enough in properties that when coextruded as layers they will become chemically bonded at the clear/color layer interface4. As such, an example polypropylene/ethylene copolymer for use in thecolor layer5 has a monomer ratio of 0.5-12% ethylene, such as 2-10%, or 3-7% ethylene. The example polypropylene/ethylene copolymer may also be isotactic, such as 60-90%, or 70-85% isotactic and have a random microstructure. The crystallinity of the example polypropylene/ethylene copolymer may be greater than 60%, such as greater than 70%, or greater than 90%. The example copolymer may have a Rockwell hardness of greater R100, such as R105 or greater. The melting point of the example copolymer is greater than 155° C., such as 156° C. to 300° C., 156° C. to 170° C., or 156° C. to 165° C. The example polypropylene/ethylene copolymer may have a flexural modulus of greater than 1000 MPa, such as greater than 1850 MPa, for example as 1900 to 2500 MPa, or 2000 to 2100 MPa. A blend of polyolefins may also be employed in thecolor layer5; for example, a blend of majority isotactic polyolefin and a minority of syndiotactic or atactic polyolefin. Example isotactic polyolefins include those sold under the following trade names: INSPIRE 404 polypropylene (Dow), CLYRELL RC514 L (LyondellBasell), INSPIRE 117 polypropylene (Dow), SR257M (LyondellBasell), 6289MZ (Total), 6D83K (Dow), and PRISMA 3410 polypropylene (Braskem). Example syndiotactic polyolefins include those sold under the following trade names: Polypropylene 1251 (Total Petrochemicals) (2 MI, 6.9% Haze, 130° C. melt point) and Polypropylene 1471 (Total Petrochemicals) (4 MI, 4.8% Haze, 130° C. melt point). Another example polyolefin is NOTIO from Mitsui Chemicals (Haze 4-7%,melt point 100° C.-135° C.). An example atactic polypropylene is FF018F from Sunoco (1.8 Melt Flow g/10 min at 230 C with 2.16 kg weight). A metallocene-based homopolymer or copolymer of propylene may also be used. Additives, such as UV stabilizer, e.g. CYASORB THT 7001, Antioxidants, e.g. HOSTANOX PEP-Q (Clariant), and slip agents, e.g. CRODAMIDE ER (Croda), may also be added to the polyolefin.
• Thecolor layer5 contains pigment, including opaque pigments, translucent pigments, and special effect pigments such as metal flake, pearlescent, fluorescent, phosphorescent, & mirrored glass. Typically, thecolor layer5 will be essentially opaque, such as 10% to 0%, 5% to 0.1%, or 1% to 0.01% light transmittance.
• Regarding the pigmentation of the color layer5 (and other polyolefin layers when desired), the pigment is introduced into thelayer5 as a pigment/carrier pre-dispersion. The carrier and pigment are mixed in a pre-dispersion, and then added to thecolor layer5 polyolefin before coextrusion. The carrier is a polymer resin that is selected based on its ability to mix well with the polyolefin and pigment and not negatively affect the properties of the structure, during or after processing. Pigments compatible with the pigment pre-dispersions disclosed herein include organic and inorganic pigments. Examples of the types of pigments that can be included in such a pigment pre-dispersion include, but are not limited to, carbon black, titanium dioxide, zinc oxide, calcium carbonate, black iron oxide, red iron oxide, yellow iron oxide, green iron oxide, mixed metal oxides, bismuth vanadate, phthalocyanine blue, phthalocyanine green, quinacridone reds, anthraquinone, perylene reds, polyazos, or mixtures thereof. Generally, organic pigments are smaller and more difficult to disperse than inorganic pigments. Examples of resins compatible with polyolefins for use in the claimed pigment pre-dispersions include, ethylene/acrylic acid copolymer waxes, ethylene/acrylic acid copolymer resins, ethyl methyl acrylate copolymer, and polypropylene/ethylene copolymers, such as TC-110 EMA (Exxon Mobil), AC540 wax (Honeywell), INSPIRE 404, and PRIMACOR 1410 (Dow).
• Many factors can affect the choice of a carrier resin for use in a pigment pre-dispersion. Specifically at issue is the compatibility of a carrier resin with the polyolefin into which it will be blended. The refractive index of a carrier resin compatible with a polyolefin may be very close to the refractive index of the polyolefin, e.g., within 0.005 of the refractive index of the polyolefin (sodium-D filter at 20° C.). Typically, it is advantageous to select a carrier resin with a melt flow rate that is greater than or equal to the melt flow rate of the polyolefin when measured at the same temperature and load as the polyolefin. Melt flow rate may be measured, for example, according to ASTM D1238. Furthermore, a carrier resin should also be compatible and miscible with the polyolefin into which it will be blended. The appearance properties of the final product improve as the compatibility between the carrier resin and the polyolefin increases.
• The particle size of the pigment should generally be minimized to optimize dispersion of the pigment in the polyolefin. As different pigments are unique compounds having widely varying sizes and molecular properties, there is no single size that can be suggested as optimal. Generally, the quality of the dispersion achieved upon mixing a pigment pre-dispersion with a polyolefin will be improved with smaller pigment particles. Typically, pigment particle sizes in a pigment pre-dispersion of less than or equal to about 25 micrometers are capable of being well dispersed. Thus, the pigments used in the multilayer structure should have a particle size of less than or equal to about 25 micrometers, such as 25 micrometers, 15 micrometers, or 10 micrometers.
• The pre-dispersion can be made as described in the co-owned U.S. application Ser. No. 11/592,883, titled, “Ionomer Pigmentation,” which is hereby incorporated by reference.
• The pigment pre-dispersion may be added to the polyolefin as the polyolefin is processed in an apparatus such as an extruder. The pigment pre-dispersion can be pre-mixed with polyolefin pellets or powder prior to the polyolefin being added to the processing apparatus. Additionally, the pigment pre-dispersion can be let down into an intermediate carrier and this intermediate mixture can then be blended with the polyolefin. If let down into an intermediate carrier, the pigment pre-dispersion level can be, for example, about 25% to about 50% of the intermediate mixture. The intermediate mixture may then be mixed with a polyolefin at a level, for example, of about 2% to about 10% of the polyolefin.
• Theexample backing layer7 ofFIG. 1 is 1 to 500 mils in thickness, for example 3 to 500 mils, 10 to 300 mils, or 100 to 200 mils. Theexample backing layer7 is primarily composed of a thermoplastic polyolefin, such as polypropylene/ethylene copolymer. The thermoplastic polyolefin is preferably of a random microstructure, and may be exclusive of block copolymers. Example random isotactic polyolefins include high-impact copolymers, for example those having 7 to 30% ethylene homo or copolymer content, such as Pro-Fax 7823 PP (LyondellBassell). Other example random isotactic polyolefins include those sold under the following trade names: INSPIRE 404 polypropylene (Dow), CLYRELL RC514 L (LyondellBasell), INSPIRE 117 polypropylene (Dow), SR257M (LyondellBasell), 6289MZ (Total), 6D83K (Dow), and PRISMA 3410 polypropylene (Braskem). Example random syndiotactic polyolefins include those sold under the following trade names: Total Polypropylene 1251 (2 MI, 6.9% Haze, 130° C. melt point) and Total Polypropylene 1471 (4 MI, 4.8% Haze, 130° C. melt point). Another example polyolefin is NOTIO from Mitsui Chemicals (Haze 4-7%,melt point 100° C.-135° C.). A metallocene-based homopolymer or copolymer of propylene may also be used.
• The example backing layer also may contain an elastomer, such as, for example, ethylene alpha-olefin copolymers where the alpha-olefin portion can contain 3-20 carbon atoms. Examples of such materials include but are not limited to ethylene octene copolymer, ethylene butene copolymer, ethylene hexene copolymer, ethylene heptene copolymer. These type of alpha olefins represent the following PE families: LDPE, VLDPE, ULDPE. Additional elastomers include, but are not limited to, ethylene propylene copolymer, ethylene propylene diene terpolymer, ethylene alpha-olefin diene terpolymer, styrenic block copolymer including styrene-butadiene-styrene and styrene-ethylene-propylene-styrene. The very low density polyethylene rubber may have a density of 0.75 to 0.95 g/cm³, such as about 0.88 g/cm³. Preferably, thebacking layer7 and thecolor layer5 will have like chemistries, e.g. olefinic. Anexample backing layer7 includes 40-95%, 60-80%, such as 55-70%, of a propylene/ethylene copolymer, the propylene/ethylene copolymer may have a monomer ratio of 0.5-12% ethylene, such as 1-7%, 2-10%, or 3-7% ethylene. The elastomer component when present may make up 50% or less of the backing layer, such as 5-40%, 10-35%, or 6-10%.
• A filler, such as talc may constitute 0-40%, such as 20-30%, or 22-28% of the example backing layer. Furthermore, various other additives such as process aids, dispersing aids, UV stabilizers, antioxidants, and nucleators may also be utilized in the backing layer in small amounts, such as 0.001% to 10%, 0.01% to 5.0%, or 0.1 to 3.5%. Examples of such additives include TR016 wax (Struktol) (process aid & dispersing aid), CHIMASSORB 119 (Ciba) (UV stabilizer), SYNPRO 12B calcium stearate (Ferro) (process aid & dispersing aid), IRGANOX3114 (Ciba) (antioxidant), HOSTANOX PEP-Q (Clariant) (antioxidant), VANOX ZMTI (R.T. Vanderbilt) (antioxidant), and HPN 20E (Milliken) (nucleator). Thebacking layer7 may also include pigment and/or effect materials in some applications.
• FIG. 2 shows an example sheet structure that is similar toexample structure1 shown inFIG. 1, however, the sheet structure ofFIG. 2 is amultilayer tape structure10. Although the examplemultilayer tape structure10 itself is coextruded, thetape structure10 may be applied to a substrate during a lamination process. In this case, themultilayer tape structure10 would be laminated to another substrate prior to, during, or after the forming of an article. In order to achieve good adhesion after lamination, thebacking layer17 in this structure may contain an additional adhesive component that will have a lower melting point compared to the other existing olefinic ingredients. The lamination may be by melt lamination or by an additional laminated adhesive layer. Examples of laminated adhesive layer include pressure-sensitive tape, roll-applied adhesive, and two-sided tape. It is also possible to omit the adhesive component if thebacking layer17 will adhere to a desired substrate sufficiently without the adhesive. As adhesive components are added to thebacking layer17, the addition of a release liner, such as the mask layers described in the commonly owned WIPO Publication WO 2006/014281, titled “Co-extruded Mask Layer,” which is hereby incorporated by reference, may be helpful in order to prevent the roll from sticking to itself. Amultilayer tape structure10 as thin as 3 mils to as thick as 25.0 mils, such as 5.0 mils to 25.0 mils may be created.Multilayer tape structures10 of intermediate thicknesses may also be created, for example, 10.0 to 20.0 mil, or 12.0 to 18.0 mils.
• The exampleclear layer13 ofFIG. 2 is 1 to 10.0 mils in thickness, for example 2.0 to 10.0 mils, 3.0 to 8.0 mils, or 4.0 to 6.0 mils. Otherwise, the exampleclear layer13 of thetape structure10 is essentially the same as the exampleclear layer3 ofFIG. 1, described above.
• Theexample color layer15 ofFIG. 2 is 1 to 10 mils in thickness, for example 2.0 to 10.0 mils, 3.0 to 8.0 mils, or 4.0 to 6.0 mils. Otherwise, theexample color layer15 of thetape structure10 is essentially the same as theexample color layer5 ofFIG. 1, described above.
• Theexample backing layer17 ofFIG. 2 is 1 to 5.0 mils in thickness, for example 1.5 to 4.5 mils, or 2.0 to 4.0 mils. Theexample backing layer17 of thetape structure10 is essentially the same as theexample backing layer7 ofFIG. 1, described above, except it contains an adhesive as part of the polymeric blend. The adhesive component may be used in practically any weight percentage in the backing structure, for example, 60 to 100%, 20-60%, 30-50%, or 35-45%. The adhesive component may be olefinic polymers, or copolymers such as polypropylene/ethylene copolymers with a high level of ethylene monomer content, and a low melting point, for example, ethylene alpha-olefin copolymers where the alpha-olefin portion can contain 3-20 carbon atoms. Examples of such materials include, but are not limited to, ethylene octene copolymer, ethylene butene copolymer, ethylene hexene copolymer, ethylene heptene copolymer. These type of alpha olefins represent the following polyethylene families: LDPE, VLDPE, ULDPE. Additional elastomers include, but are not limited to, ethylene propylene copolymers, ethylene propylene diene terpolymer, ethylene alpha-olefin diene terpolymer, styrenic block copolymers including styrene-butadiene-styrene, styrene-ethylene-propylene-styrene and the like, a particular example of ethylene-propylene elastomer is VERSIFY 2300 (Dow). The adhesive component could also include, but is not limited to, other olefinic or non-olefinic materials such as ethylene-acrylate-GMA terpolymers, ethylene butyl (or methyl or hexyl)acrylate copolymers, EVA, ester and ether based urethanes, ethylene acid copolymers, and maleic anhydride grafted copolymers.
• Varying the type of adhesive component in polymeric blend allows the multilayer structure to be laminated to different substrates, including, but not limited to: polypropylene, TPO, polyethylene, a polymeric blend or alloy containing polypropylene or polypropylene in it, ABS, ABS containing blends or alloys, acrylic, polycarbonate, polycarbonate containing blends or alloys, metal, glass, wood, ceramic, thermoset plastics, and composites. Theadhesive layer17 may be provided with pigment and/or effect material.
• FIGS. 3 and 4 depict the four-layer structure20,30 counterparts of the three-layer structures1,10 ofFIGS. 1 and 2. As such, the four-layer structures20,30 are used in substantially the same manner as described forFIGS. 1 and 2, respectively, and are similar in composition, except as noted below. The four-layer structures20,30 inFIGS. 3 and 4 each have aclear layer23,33, acolor layer25,35, and abacking layer27,37. The structures ofFIGS. 3 and 4, however, differ from the structure ofFIGS. 1 and 2 in that each has atranslucent color layer29,39 between the clear23,33 andcolor layers25,35. Thetranslucent color layer29,39 is primarily made of a polyolefin, such as polypropylene/ethylene copolymer. An example polypropylene/ethylene copolymer for use in thetranslucent color layer29,39 has a monomer ratio of 0.5-12% ethylene, such as 2-10%, or 3-7% ethylene. The example polypropylene/ethylene copolymer may also be isotactic, such as 60-90%, or 70-85% isotactic and have a random microstructure. The crystallinity of the example polypropylene/ethylene copolymer may be greater than 60%, such as greater than 70%, or greater than 90%. The example copolymer may have a Rockwell hardness of greater R100, such as R105 or greater. The melting point of the example copolymer is greater than 155° C., such as 156° C. to 300° C., 156° C. to 170° C., or 156° C. to 165° C. The example polypropylene/ethylene copolymer may have a flexural modulus of greater than 1000 MPa, such as greater than 1850 MPa, 1900 to 2500 MPa, or 2000 to 2100 MPa. A blend of polyolefins may also be employed in thetranslucent color layer29,39; for example, a blend of majority isotactic polyolefin and a minority of syndiotactic or atactic polyolefin. Example random isotactic polyolefins include those sold under the following trade names: INSPIRE 404 polypropylene (Dow), CLYRELL RC514 L (LyondellBasell), INSPIRE 117 polypropylene (Dow), SR257M (LyondellBasell), 6289MZ (Total), 6D83K (Dow), and PRISMA 3410 polypropylene (Braskem). Example random syndiotactic polyolefins include those sold under the following trade names: Polypropylene 1251 (Total)(2 MI, 6.9% Haze, 130 C melt point) and Polypropylene 1471 (Total)(4 MI, 4.8% Haze, 130 C melt point). Another example polyolefin is NOTIO from Mitsui Chemicals (Haze 4-7%, Melt point 100 C-135 C). An example atactic polypropylene is FF018F from Sunoco (1.8 Melt Flow g/10 min at 230 C with 2.16 kg weight). A metallocene-based homopolymer or copolymer of propylene may also be used. This translucent color layer may be used to create various special effects such as metal flake, pearlescent, fluorescent, phosphorescent, and mirrored glass and/or improve the depth of color for the underlying opaque color layer. The polyolefin that makes up the translucent color layer may be of the same chemistry as the clear23,33 andcolor layers25,35 to promote adhesive-free bonding at the layer interfaces24,34,26,36,28,38.
• Thetranslucent color layer29,39 does not require that only translucent pigments are used therein. In this case, “translucent” is meant to refer to the percent loading of color used in thetranslucent layer29,39. All pigments used in thecolor layer25,35 can also be used in thetranslucent layer29,39, but are used in lower amounts (relative to the underlying essentiallyopaque color layer25,35) in order to maintain some level of the base resin clarity.
• Regarding the example four-layer structure ofFIG. 3, thestructure20 may be as thin as 4.0 mils to as thick as 560 mil, such as 11 mils to 560 mils. Multilayer structures of intermediate thicknesses may also be created, for example, 20 mils to 450 mil, 50 mils to 300 mil, or 150 mils to 250 mils. Relatively thick sheets may be used in applications where it is desired to thermoform a part directly from the sheet itself, or thinner sheets may be desirable to thermoform a shell that is suitable to be backfilled via injection molding to achieve the final thickness. Thetranslucent layer29 may be 1 to 20 mils in thickness, such as 2.5 to 20 mils, 5.0 to 15 mils, or 7.0 to 12.0 mils.
• Regarding the example four-layer tape structure30 ofFIG. 4, thestructure30 may be as thin as 4 mils to as thick as 35.0 mils. Multilayer structures of intermediate thicknesses may also be created, for example, 7 mils to 35 mils, 8.0 mils to 30.0 mils, 10 mils to 20.0 mils, or 12.0 mils to 18.0 mils. Thetranslucent layer39 is 1 to 10 mils in thickness, for example 2.0 to 10 mils, 3.0 to 8.0 mils, or 4.0 to 6.0 mils. As with thetape structure10 ofFIG. 2, the four-layer tape structure30 would be laminated to another substrate prior to or during the forming of an article. In order to achieve good adhesion after lamination, thebacking layer37 in thisstructure30 may contain an additional adhesive component that will have a lower melting point compared to the other existing olefinic ingredients.
• FIG. 5 depicts an example twolayer structure40 that includes aclear polyolefin layer43 over acolored backing layer47. Theclear layer43 has the same characteristics as the exampleclear layer3 ofFIG. 1, except that it is coextruded with and permanently bonded directly to thecolored backing layer47 at alayer interface44. Thecolored backing layer47 is the same as thebacking layer7 ofFIG. 1, except it is provided with pigment and/or effect materials. Carrier resins may also be used to incorporate the pigment and/or effect materials into thecolored backing layer47. Example carrier resins, pigments, and effect materials may be selected from those listed above in the discussion of thecolor layer7 ofFIG. 1. The carrier resin, however, should be carefully selected to be compatible with the majority component polymer of thecolored backing layer47. That is, the carrier resin should have similar melt flow rate, refractive index, and be miscible in the majority component polymer. The pigment and/or effect materials may be incorporated into thecolored backing layer47 in an amount of 0.0001% to 30%, for example, 0.01% to 20%, 1.0% to 10%, or 0.0001% to 0.01%.
• In an alternative example, theclear polyolefin layer43 may be replaced with a colored layer as described above having pigments and/or effect materials.
• Some examples of different formed products in which this two layer structure is used include: RV exterior wall panels, heavy truck and RV air cones, fenders or body panels for agricultural vehicles, and truck farings.
• Thestructures1,10,20,30,40 shown inFIGS. 1-5 may be used with or without a mask layer, such as a protective mask, forming mask, or combination of protective/forming mask, for example, the mask layers described in WIPO Publication WO 2006/014281. The mask layer could be laminated onto or coextruded with the structures illustrated inFIGS. 1-4.
• In order to improve or modify the performance of an individual layer or the structure as a whole, each layer shown inFIGS. 1-5 may contain additive ingredients from the following list in any combination. The list is as follows:
• Antioxidants
• UV stabilizers
• Waxes as Property Modifiers
• Lubricants
• Antistats
• Process Aids
• Dispersion Aids
• Flame Retardants
• Smoke Suppressors
• Foaming Agents
• Colorants (pigments, dyes, all special effect additives)
• Antimicrobials
• Antiblock Agents
• Fiber Additives
• Plasticizers (e.g. polypropylene plasticizers such as Elevast or polyethylene-glycol)
• Antifog Agents
• Clarifying Agents
• Nucleating Agents
• Acid Scavengers
• Low Temperature Impact Modifiers
• Fillers (inorganic & wood)
• Gloss Agents
• Gloss Reducing Agents
• Scratch Mar Additives
• Stress Whitening Modifiers
• Surfactants
• Silicone, Siloxanes, Organo-Modified Siloxanes, or Silicone Graft Copolymers (e.g., Evonik Tegomer which may contain alkyl, epoxide, hydroxy, amino, carboxyl, and/or acrylate organic substituents)
• Functional grafted polypropylene modifiers (e.g. acid grafted polypropylene, maleic anhydride grafted polypropylene, and ionic functional grafted polypropylene)
• In particular, one or more clarifying agents may be added to polymers that are already clarified by various methods or the clarifying agents may be added to non-clarified polymers. Stress whitening agents may be added to improve blush resistance.
• The aforementioned additives may also be utilized in each layer in relatively small amounts, such as 0.0001% to 10%, 0.0001% to 0.001%, 0.0001 to 1%, 1% to 5%, and 5% to 10%, and for fillers, fibers, retardants, functional grafted polypropylene modifiers, and smoke suppressor additives, up to 50%, such as up to 40%, or 10-30%.
• The example multilayer structures are not substantially oriented either axially or biaxially by stretching. By not substantially oriented, it is meant that the polymers are not purposely stretched to induce orientation that would affect the physically properties of the material. The multilayer structure may have a flexural modulus of 1000 MPa or greater, such as 1500 to 7000 MPa, 1700 to 3000 MPa, 3000 to 6000 MPa, or 2500 to 5500 MPa.
• The example multilayer structures display excellent optical qualities. The example multilayer structures have a distinction of image (DOI) of at least 70, such as 75 or greater, 85 or greater, 90 or greater, and 95 or greater. Furthermore, the multilayer structures have a gloss of 75 or greater at a 60° angle, such as 85 or greater, 90 or greater, and 95 or greater. The multilayer structures also have a gloss of 60 or greater at a 20° angle, such as 70 or greater, 80 or greater, and 85 or greater.
• The example multilayer structures also posses excellent durability and mar resistance, exemplified by several tests required by auto manufacturers (see Table 2 below). For instance, the multilayer structures will pass a five-finger scratch and mar resistance test defined by GMW 3943. The structures also exhibit no gauze imprint at 70° C. minimum under a 500 g load applied over a 40 mm diameter for two hours. Furthermore, the multilayer structures show no signs of gloss loss, staining, or surface swelling at 70° C. with exposure to methanol, motor oil, lithium grease, and egg albumin.
• The multilayer structures can be thermoformed into formed products, such as, for example, an automobile bumper or other exterior trim panel. Such a part can be made from a multilayer structure that is thick enough to provide sufficient structural stability to be used alone. Furthermore, the multi-layer structure can be injection molded from behind with additional polymer material to provide support to the multilayer structure. The pigmented polyolefins with their minimized pigment particle size are able to maintain color uniformity and opacity in high draw regions created during thermoforming.
• The layers of the multilayer structures are coextruded and include those layers shown inFIGS. 1-5 and described herein. Additional co-extruded layers can include, but are not limited to, polymers such as polypropylene, polypropylene copolymer, polyethylene, polyethylene copolymer, polyamide, polyester, ABS, styrene terpolymer, and polyurethane.
• The polyolefin layers and multilayer films as described herein may be exposed to various structure modifying treatments to further enhance aspects of physical performance. These products may, for example, be subjected to corona discharge treatment, ozone treatment, low temperature plasma treatment which incorporates either oxygen or nitrogen gas, glow plasma treatment, reverse sputtering treatment, oxidation treatment using chemicals, UV curing, e-beam irradiation, gamma beam irradiation, x-rays and the like. Such treatments may, among other things, cross-link the polymer structure of the polyolefin layers and the multilayer films. As an example, the multilayer films could be exposed to gamma beam, electron beam, or x-ray radiation at dosing levels of between 0.1 and 50 meg-rads. These treatments can improve the surface hardness, scratch resistance, mar resistance, chemical resistance and/or oxygen/air barrier efficiency of the multilayer structures while maintaining low haze, high gloss, transparency, and distinction of image. Additionally, weathering performance can be maintained or enhanced and material memory can be maintained. These treatments may also improve the adhesion properties of thetape structures10,30 to various substrates.
• The improvements realized in the multilayer structures described herein in both design and durability performance allow them to be used in a variety of markets which require a “Class A” finish, such as:
• Motor Vehicles
• Light/Consumer Automotive
• Heavy Trucks
• RV
• Agriculture
• ATV's
• Motorcycles
• Snowmobiles
• Jet Skis
• Marine
• Farm Machinery
• Signage
• Appliances
• Consumer Electronics.
• Example articles the multilayer sheets could be formed into include:
• Bumper fascias
• Rocker panels
• Cell-Phone covers
• Computer housings
• Motor covers
• Fenders
• Heavy truck fairings
• Running boards
• RV wall panels
• Appliance housings.
• FIGS. 6 and 7 show example cross-sections of vehicle body panels constructed of the multilayer structure of the present disclosure. InFIG. 6, the multilayer film has aclear layer53, acolor layer55, and abacking layer57, and the multilayer film is laminated onto arigid substrate59. InFIG. 7, themultilayer structure60 has aclear layer63, acolor layer65, and abacking layer67. Themultilayer structure60 is thick and rigid enough to be a vehicle body panel without an additional rigid substrate. The translucent layer discussed above may also be used in combination with or in place of the colored layer on vehicle body panels. Also, the colored backing layer may be used in place of the backing layer and with only a clear layer on top in vehicle body panels.
• In an additional example, thestructures1,10,20,30 inFIGS. 1-4 andstructures40,50, and60 inFIGS. 5-7 utilize regrind as an additional layer adjacent to the backing layer or as a component of the backing layer. As explained below, the example backing layer provides significant and unexpected advantages over backing layers that mix regrind and virgin polymer in one layer.
• Thermoforming TPO sheet is typically difficult due to the material's inherently weak melt strength. Inadequate melt strength during heating results in excessive “sheet sag,” which in turn can cause various defects during forming of the part. Defects include excessive “webbing” in tight corners, surface “tears” in areas of high stretch, and non-uniform wall thickness. Significant variation in wall thickness throughout a part can cause excessive warping and/or reduced physical properties.
• During sheet production, the melt strength of TPO is further compromised due to the addition of regrind which causes an increase in the severity of the above mentioned defects. The addition of regrind is performed in order to control costs by minimizing waste and reducing the overall raw material cost of the final part. Although the economics improve with the addition of regrind, the melt strength, sag resistance, and other properties of the sheet are significantly reduced.
• It was unexpectedly discovered that the reduction of melt strength and sag resistance due to the addition of regrind can be significantly reduced by changing the structure of the TPO sheet.
• As shown inFIGS. 8 and 9 the thermoplastic polyolefin backing layer has multiple layers as components. There is a separate layer of virgin thermoplastic polyolefin material (Layer A) and a separate layer of regrind thermoplastic polyolefin material (Layer B).FIG. 8 shows anexample sheet structure70 with an ABA multilayered backing layer structure andFIG. 9 shows anexample sheet structure80 with an ABbacking layer structure80.
• Theexample sheet structure70 inFIG. 8 has an ABA backing layer made up of afirst A layer71, asecond A layer73, and aB layer72 disposed between the first and second A layers71,73. First Alayer71 is adjacent to one side of theB layer72 and thesecond A layer73 is adjacent to the opposite side of theB layer72. The ABA backing layer is combined with anupper section75 that comprises a clear layer and optionally a translucent and/or color layer, as those layers are described above and are depicted instructures1,10,20,30,40,50,60 shown inFIGS. 1-7. Thefirst A layer71 is adjacent to theupper section75.
• The polymeric base for first Alayer71 and thesecond A layer73 of theexample sheet structure70 ofFIG. 8 is 100% virgin thermoplastic polyolefin. Virgin thermoplastic means a thermoplastic that has not been reprocessed and/or previously used in another product. The thermoplastic polyolefin may be selected from the thermoplastic polyolefins described above for thebacking layer7 ofFIG. 1. Additives may also be included as described herein for the backing layer.
• Thefirst A layer71 is, for example, 5% to 45% of the total thickness of the ABA backing layer, such as 10 to 35%, 5 to 20%, or 25 to 45% of the total backing layer thickness. The entire example ABA backing layer structure is 3.0 to 500 mils, so thefirst A layer71 may be 0.15 mils to 225 mils, such as 5 to 10 mils, 10-80 mils, or 20 to 150 mils. Thesecond A layer73 has the same range of thicknesses, however, its thickness is independently selected from the thickness of thefirst A layer71.
• The polymeric base for theB layer72 is 100% regrind polyolefin material (meaning a polyolefin that has been previously used and/or reprocessed). If desired for certain applications, theB layer72 may also be a mixture of regrind and virgin polymeric material. For example, the polymeric base for the B layer may comprise 10 to 99% regrind, such as 10 to 49%, 51 to 99%, or 25 to 75% regrind material, whereas the remainder of the polymeric base is virgin polyolefin material.
• The regrind material is produced from sources such as trim scrap, products that do not meet quality control or specifications, or various other sources that would otherwise be waste materials. The original polymer used in the regrind material may, for example, be selected from the thermoplastic polyolefins described above for thebacking layer7 ofFIG. 1. The original material used for the regrind material may also include additives as described herein for the backing layer. In one example, the regrind material is miscellaneous polypropylene homopolymers and copolymers with talc filler, colorants, and stabilizers.
• TheB layer72 is, for example, 10-90% of the total thickness of the ABA backing layer, such as 10 to 49%, 51 to 90%, or 20 to 60% of the total backing layer thickness. The entire example ABA backing layer structure is 3.0 to 500 mils, so theB layer72 may be 0.3 mils to 450 mils, such as 5 to 20 mils, 20-120 mils, or 40 to 300 mils.
• In an alternate example, thefirst A layer71 and optionally thesecond A layer73 also include a pigment to supply the layer with a desired color. This colored backing layer is particularly suitable for use with anupper section75 that includes only a clear layer. This can be considered a two-layer structure as described above and shown inFIG. 5, although the backing layer is divided into three separate layers.
• Theexample sheet structure80 shown inFIG. 9 has an AB backing layer made up of anA layer81 and aB layer83. The AB backing layer is combined with anupper section85 that comprises a clear layer and optionally a translucent and/or color layer, as those layers are described above, and are depicted instructures1,10,20,30,40,50,60 shown inFIGS. 1-7. TheA layer81 is adjacent to theB layer83 on one side and is adjacent to theupper section85 on the other side.
• TheA layer81 andB layer83 are composed of the same materials as disclosed for the ABA layer example shown inFIG. 8. Coloring may also be added to theA layer81 as described above, particularly when the AB backing layer is used in conjunction with just a clear layer in theupper section85.
• TheA layer81 is, for example, 10-90% of the total thickness of the AB backing layer, such as 20-60%, 10 to 49%, or 51-90% of the total backing layer thickness. The entire example AB backing layer structure is 3.0 to 500 mils, so theA layer81 may be 0.3 mils to 450 mils, such as 5 to 20 mils, 20-120 mils, or 40 to 300 mils.
• TheB layer83 is, for example, 10-90% of the total thickness of the AB backing layer, such as 20-60%, 10 to 49%, or 51-90% of the total backing layer thickness. The entire example AB backing layer structure is 3.0 to 500 mils, so theB layer83 may be 0.3 mils to 450 mils, such as 5 to 20 mils, 20-120 mils, or 40 to 300 mils.
• The ABA and AB backing layers may be formed by coextrusion. The ABA and AB backing layers can be coextruded with the upper section that includes a clear layer and optionally a color and/or translucent layer. In another example, further thermoplastic polyolefin layers may be added. For example, the backing layer may be structured as an ABABA layered structure.
• Theexample sheet structure70,80 may also be used in conjunction withupper sections75,85 that comprise chemistries other than the polyolefin layers described above. For example, theupper sections75,85 may comprise polymeric components such as acrylic, ionomer, fluoracrylic, fluoropolymers, cast-fluoroacrylic, polystyrene, polyethylene, polycarbonate, acrylic styrene acrylonitrile (ASA), or mixtures thereof. These alternative upper section chemistries could also be extruded or laminated onto the ABA backing layer. In certain embodiments theupper sections75,85 could even be paint.
Examples 1-6
• Example 1 is a prospective, generic example, and is set forth to demonstrate an example range of different ingredients that may be added to each layer of the multilayer structure. The optimal concentration and presence of these ingredients will vary based on the color and type of pigment desired. Other application specific parameters may also affect the composition of the multilayer structure.
Prospective Generic Example 1Clear Layer
• 70-100% Inspire 404 Clear PP* *Inspire 404 PP is a highly isotactic, highly crystalline polypropylene/ethylene copolymer containing about 1-7% ethylene monomers, and having a flexural modulus of 2070 MPa (⅛ inch bar), 156° C. melting point, 95.6 J/g enthalpy of melting, Rockwell C hardness)
• 0-3.0% UV Stabilizer e.g. Cyasorb THT 7001
• 0-10.0% Slip Agent e.g. Crodamide ER (an effective amount that does not impact haze detrimentally)
• 0-3% Clarifier, e.g. NX20
• 0-1.0% Antioxidant, e.g. Hostanox Pep-Q
• 0-1.0% Second Antioxidant, e.g. Irganox 3114
• Translucent Color Layer (this Layer is Optional & the Formula Varies with Color & Special Effects)
• 60.000-99.000% Polypropylene, e.g. Inspire 404 PP*
• 0-1.0% Antioxidant, e.g. Hostanox Pep-Q
• 0-3% Clarifier, e.g. NX20
• >0-10.000% pigment &/or special effects
• 00.000-20.000% Color carrier 1 e.g. LLDPE purchased from Lancer Dispersions
• 00.000-20.000% Color carrier 2, e.g. Ethylene Acid Copolymer
• 00.000-20.000% Color carrier 3, e.g. AC540 Wax
• 00.000-20.000% Color carrier 4, e.g. Inspire 404 PP
• 00.000-3.00% UV Stabilizer, e.g. Cyasorb THT 7001
• 0-1.0% Antioxidant, e.g. Irganox 3114
• Color Layer (this Formula Varies with Color & Special Effects)
• 50.000-95.000% Polypropylene, e.g. Inspire 404 PP*
• 0-3% Clarifier, e.g. NX20
• 0-1.0% Antioxidant, e.g. Hostanox Pep-Q
• >0-20.000% Pigment &/or special effects
• 00.000-25.000% Color carrier 1, e.g. LLDPE
• 00.000-25.000% Color carrier 2, e.g. Ethylene Acid Copolymer
• 00.000-25.000% Color carrier 3, e.g. AC540 Wax
• 00.000-25.000% Color carrier 4, e.g. Inspire 404 PP
• 00.000-3.00% UV Stabilizer, e.g. Cyasorb THT 7001
• 0-1.0% Second antioxidant, e.g. Irganox 3114
• Backing Layer
• 40-95% Polypropylene, e.g. Pro-Fax 7823 PP** **Pro-Fax 7823 PP is a polypropylene/ethylene copolymer, Rockwell 80R scale, flexural modulus of 1120 MPa by ASTM D790, melting point greater than 120° C.
• 0-60% Rubber, e.g. DFDB 1088NT VLDPE
• 0-40% Talc Filler, e.g. Premium HTP Ultra 5 L
• 0-2% Process aid and dispersing aid, e.g. TR016 Wax
• 0-3% UV stabilizer, e.g. Chimassorb 119
• 0-2% Second process aid and dispersing aid, e.g. Synpro 12B Calcium Stearate
• 0-1% Antioxidant, e.g. Irganox 3114
• 0-1% Second Antioxidant, e.g. Hostanox Pep-Q
• 0-1% Third Antioxidant, e.g. Vanox ZMTI
• 0-0.5% Nucleator, e.g. HPN 20E
• 0-8.000% Pigment or Color Concentrate (A. Schulman)
• Examples 2-6 are actual, non-generic examples, optimized for certain pigments.
Example 2Three-Layer Structure
• Clear Layer
• 96.1% Inspire 404 Clear PP*
• 00.3% Cyasorb THT 7001 (UV stabilizer)
• 00.3% Crodamide ER (slip agent)
• 3% NX20 (Milliken Chemical) (clarifier)
• 0.300% Hostanox Pep-Q (antioxidant)
• Color Layer
• 90.280% Inspire 404 PP*
• 3% NX20 (clarifier)
• 4.000% AC540 Wax (organic pigment carrier)
• 0.360% TC-110 EMA (inorganic pigment carrier)
• 0.040% Red Iron Oxide 116M (Nubiola) (pigment)
• 0.720% Perylene Red 179 229-8436 (Sun Chemical) (pigment)
• 1.000% DPP Red 254 Cromophtal 2030 (Ciba) (pigment)
• 0.300% Cyasorb THT 7001 (UV Stabilizer)
• 0.300% Hostanox Pep-Q (antioxidant)
• Backing Layer
• 61.944% Pro-Fax 7823 PP**
• 7.680% DFDB 1088NT VLDPE (Dow Chemical)
• 24.48% Premium HTP Ultra 5 L talc filler (Imi Fabi)
• 0.576% TR016 Wax (process aid & dispersing aid)
• 0.288% Chimassorb 119 (UV stabilizer)
• 0.048% Synpro 12B Calcium Stearate (process aid & dispersing aid)
• 0.288% Irganox 3114 (antioxidant)
• 0.288% Hostanox Pep-Q (antioxidant)
• 0.288% Vanox ZMTI (antioxidant)
• 0.120% HPN 20E (Milliken Chemical) (nucleator)
• 4.000% Schulman Gray Color Concentrate (A. Schulman)
Example 3Four-Layer Structure
• Clear Layer
• 99.1% Inspire 404 Clear PP*
• 00.3% Cyasorb THT 7001 (UV stabilizer)
• 00.3% Crodamide ER (slip agent)
• 00.3% Hostanox Pep-Q (antioxidant)
• Translucent Color Layer
• 98.700% Inspire 404 PP*
• 0.490% AC540 Wax (organic pigment carrier)
• 0.210% DPP Red 254 Cromophtal 2030 (pigment)
• 0.300% Cyasorb THT 7001 (UV Stabilizer)
• 0.300% Hostanox Pep-Q (antioxidant)
• Color Layer
• 79.400% Inspire 404 PP* 14.000% R104 TiO2 (pigment) (DuPont)
• 4.796% HB9200 propylene homopolymer (Ineos USA LLC) (pigment carrier)
• 1.204% Profax 6301 polypropylene (Lyondell Bassell) (pigment carrier)
• 0.300% Cyasorb THT 7001 (UV Stabilizer)
• 0.300% Hostanox Pep-Q (antioxidant)
• Backing Layer
• 61.944% Pro-Fax 7823 PP**
• 7.680% DFDB 1088NT VLDPE
• 24.48% Premium HTP Ultra 5 L (talc filler)
• 0.576% TR016 Wax (process aid & dispersing aid)
• 0.288% Chimassorb 119 (UV stabilizer)
• 0.048% Synpro 12B Calcium Stearate (process aid & dispersing aid)
• 0.288% Irganox 3114 (antioxidant)
• 0.288% Hostanox Pep-Q (antioxidant)
• 0.288% Vanox ZMTI (antioxidant)
• 0.120% HPN 20E (nucleator)
• 4.000% Schulman Gray Color Concentrate (A. Schulman)
Example 4Four-Layer Structure
• Clear Layer
• 96.1% Inspire 404 Clear PP*
• 3% NX20(clarifier)
• 00.3% Cyasorb THT 7001 (UV Stabilizer)
• 00.3% Crodamide ER (Slip Agent)
• 0.30% Hostanox Pep-Q (antioxidant)
• Translucent Color Layer
• 94.400% Inspire 404 PP*
• 3% NX20(clarifier)
• 1.120% AC540 Wax (organic pigment carrier)
• 0.480% PR177 (DIC) (pigment)
• 0.240% Primacor1410 (pigment carrier)
• 0.160% 9320J Hi-Lite Sparkle Orange (BASF) (special effects pigment)
• 0.300% Cyasorb THT 7001 (UV Stabilizer)
• 0.300% Hostanox (antioxidant)
• Color Layer
• 93.450% Inspire 404 PP*
• 3% NX20(clarifier)
• 0.875% AC540 Wax (organic pigment carrier)
• 0.375% BP1300 (Cabot) (carbon black) (pigment black #7)
• 2.000% Silver ET-2025 Aluminum Flake (Silberline)
• 0.300% Cyasorb THT 7001 (UV Stabilizer)
• 0.300% Hostanox Pep-Q (antioxidant)
• Backing Layer
• 61.944% Pro-Fax 7823 PP**
• 7.680% DFDB 1088NT VLDPE
• 24.48% Premium HTP Ultra 5 L (talc filler)
• 0.576% TR016 Wax (process aid & dispersing aid)
• 0.288% Chimassorb 119 (UV stabilizer)
• 0.048% Synpro 12B Calcium Stearate (process aid & dispersing aid)
• 0.288% Irganox 3114 (antioxidant)
• 0.288% Hostanox Pep-Q (antioxidant)
• 0.288% Vanox ZMTI (antioxidant)
• 0.120% HPN 20E (nucleator)
• 4.000% Schulman Gray Color Concentrate (A. Schulman)
Example 5Three-Layer Structure
• Clear Layer
• 96.900% Pristene RM2091*** ***Pristene RM2091 is an metallocene based isotactic polypropylene/ethylene copolymer, melting point 130° C., flexural modulus 1000 MPa by ISO 178.
• 1.000% Hostavin PR-31 (Clariant)
• 0.150% Hostavin VSU (Clariant)
• 0.300% Hostanox Pep-Q (antioxidant)
• 0.300% Irgastab FS-042 (Ciba)
• 0.350% Tinuvin 328 (Ciba)
• 1.000% Crodamide ER (slip agent)
• Color Layer
• 90.780% Pristene RM2091***
• 4.000% AC540 Wax (organic pigment carrier)
• 0.360% LLDPE (Lancer Dispersions) (inorganic pigment carrier)
• 0.040% Red Iron Oxide 116M (inorganic pigment)
• 0.720% Perylene Red 179 229-8436 (organic pigment)
• 1.000% DPP Red 254 CROMOPHTAL 2030 (organic pigment)
• 1.000% Hostavin PR-31 (Clariant) (UV additive)
• 0.150% Hostavin VSU (Clariant) (UV additive)
• 0.300% Hostanox Pep-Q (antioxidant)
• 0.300% Irgastab FS-042 (Ciba) (antioxidant)
• 0.350% Tinuvin 328 (Ciba) (UV additive)
• 1.000% Crodamide ER (slip agent)
• Backing Layer
• 58.704% Pro-fax 7823 PP**
• 11.520% DBDB 1088 NT VLDPE (Dow)
• 24.480% Premium HTP Ultra 5 L Talc (filler)
• 0.048% Calcium Stearate Synpro 12B 0.518% Irganox 3114 (antioxidant)
• 0.346% Doverphos F9228 (antioxidant) (Dover Chemical Corp.)
• 0.288% Chimasorb 119 (UV stabilizer)
• 0.096% Tinuvin 328 (Ciba) (UV additive)
• 4.000% Schulman Gray Color Concentrate (A. Schulman)
Example 6Two-Layer Structure with Colored TPO
• Clear Layer
• 90% Inspire 404 PP*
• 6.9% RM2091 (LyondellBasell)
• 1.000% Hostavin PR-31 (UV additive)
• 0.150% Hostavin VSU (UV additive)
• 0.300% Hostanox Pep-Q (antioxidant)
• 0.350% Tinuvin 328 (UV additive)
• 1.000% Crodamide ER (slip agent)
• Colored TPO Layer
• 62.123% Profax PP7823**
• 7.640% DFDB 1088 NT VLDPE
• 24.352% Hi Talc Premium HTP Ultra 5 L
• 0.048% Synpro 12B calcium stearate (process aid & dispersing aid)
• 0.516% Irganox 3114 (antioxidant)
• 0.344% Hostanox Pep-Q (antioxidant)
• 0.382% Tinuvin XT850 (Ciba) (UV additive)
• 03095% Tinuvin 328 (UV additive)
• 4.500% Schulman PX-1657 Ford White P Color Concentrate (A. Schulman)
(All Percentages are by Weight.)Process for Example 2
• Clear Layer
• First, an additive concentrate was made by feeding the UV stabilizer and slip agent along with about 2.4% by weight (based upon the total weight of the clear layer) of the INSPIRE 404 polypropylene copolymer to a twin screw extruder. The INSPIRE 404 polypropylene copolymer acts as a carrier resin in this stage of the process. The extruded product is a pelletized additive concentrate.
• The clear layer was then fabricated by feeding the remaining approximately 93.7% of the INSPIRE 404 polypropylene copolymer to a single screw extruder along with the additive concentrate, the clarifier, and the antioxidant. The additive concentrate makes up 3% of the total weight of the clear layer.
• Color Layer
• An additive concentrate was made for the color layer, just as described above for the clear layer, except no slip agent is present.
• Additionally, a first color concentrate was made by combining water, the organic pigments (Perylene Red 179 229-8436 and DPP Red 254 Cromophtal 2030) and organic pigment carrier (AC540 Wax). The water is displaced by the addition of the organic pigment carrier during a flushing process, as described in U.S. patent publication 2005/0282962, which is herein incorporated by reference. A second color concentrate was made by adding the inorganic pigment and inorganic carrier resin to a mill.
• The color layer was then fabricated by feeding the INSPIRE 404 polypropylene copolymer to a single screw extruder along with the additive concentrate and the first and second color concentrates.
• Backing Layer
• In a separate process, a Farrell Continuous Mixer was loaded with Pro-Fax 7823 polypropylene and the DFDB 1088NT very low density polyethylene. Talc and the other additives listed in the formula for Example 2 were added also. The product of the mixer was natural TPO in pellet form.
• The color concentrate pellets and the natural TPO pellets were then added to a single screw extruder, which produced the backing layer.
• Coextrusion Setup
• The single screw extruders for the clear, color, and backing layers were positioned so that each layer would be coextruded in a multilayer stack.
Process for Example 3
• Clear Layer
• The clear layer was made by the process described above in Example 2, but with the formula for Example 3.
• Translucent Layer
• The color concentrate was made by the same process used to make the color layer as described in Example 2, but with the pigment and carrier resin given in the formula above for Example 3.
• The translucent layer was then fabricated by feeding the INSPIRE 404 polypropylene copolymer to a single screw extruder along with the color concentrate, the antioxidant, and the UV additive.
• Color Layer
• The color layer was fabricated by feeding the INSPIRE 404 polypropylene copolymer to a single screw extruder along with the two carrier resins and one pigment, the antioxidant, and the UV additive.
• Backing Layer
• The backing layer was made by the process described above in Example 2.
• Coextrusion Setup
• The single screw extruders for the clear, translucent, color, and backing layers were positioned so that each layer would be coextruded in a multilayer stack.
Process for Example 4
• Clear Layer
• The clear layer was made by the process described above in Example 2, but with the formula for Example 4.
• Translucent Layer
• The translucent layer was made by the same process used to make the translucent layer as described in Example 3, but with the formula for Example 4.
• Color Layer
• An additive concentrate was made for the color layer, just as described above for the clear layer, except no slip agent is present.
• Additionally, a color concentrate was made by combining water, the carbon black pigment BP1300 and organic pigment carrier (AC540 Wax). The water is displaced by the addition of the organic pigment carrier during the flushing process, as described in U.S. patent publication 2005/0282962.
• The color layer was then fabricated by feeding the INSPIRE 404 polypropylene copolymer to a single screw extruder along with the additive concentrate, the color concentrate, and the aluminum flake.
• Backing Layer
• The backing layer was made by the process described above in Example 2.
• Coextrusion Setup
• The single screw extruders for the clear, translucent, color, and backing layers were positioned so that each layer would be coextruded in a multilayer stack.
Process for Example 5
• Clear Layer
• First, an additive concentrate was made by feeding the UV stabilizer, antioxidant, and slip agent along with about 6.9% by weight (based upon the total weight of the clear layer) of the INSPIRE 404 polypropylene copolymer to a twin screw extruder. The INSPIRE 404 polypropylene copolymer acts as a carrier resin in this stage of the process. The extruded product is a pelletized additive concentrate.
• The clear layer was then fabricated by feeding the remaining approximately 90% of the INSPIRE 404 polypropylene copolymer to a single screw extruder along with the additive concentrate. The additive concentrate makes up about 10% of the total weight of the clear layer.
• Color Layer
• An additive concentrate was made for the color layer, just as described above for the clear layer of Example 5.
• Additionally, a first color concentrate was made by combining water, the organic pigments (Perylene Red 179 229-8436 and DPP Red 254 Cromophtal 2030) and organic pigment carrier (AC540 Wax). The water is displaced by the addition of the organic pigment carrier during a flushing process, as described in U.S. patent publication 2005/0282962.
• A second color concentrate was made by adding the inorganic pigment and inorganic carrier resin (LLDPE) to a mill.
• The color layer was then fabricated by feeding the INSPIRE 404 polypropylene copolymer to a single screw extruder along with additive concentrate and the first and second color concentrates in the amounts shown in the formula above.
• Backing Layer
• In a separate process, a Farrell Continuous Mixer was loaded with Pro-Fax 7823 polypropylene and the DFDB 1088NT very low density polyethylene. Talc and the other additives listed in the formula for Example 5 were added also. The product of the mixer was natural TPO in pellet form.
• The color concentrate pellets and the natural TPO pellets were then added to a single screw extruder, which produced the backing layer.
• Coextrusion Setup
• The single screw extruders for the clear, color, and backing layers were positioned so that each layer would be coextruded in a multilayer stack.
Process for Example 6
• Clear Layer
• The clear layer was made by the process described above in Example 2, but with the formula for Example 6.
• Colored Backing Layer
• The colored backing layer was made by the process described above in Example 2, but with the formula for Example 6.
• Coextrusion Setup
• The single screw extruders for the clear and colored backing layers were positioned so that each layer would be coextruded in a multilayer stack.
Results
• Table 1 summarizes the advantages over competitive technologies in terms of design simplification, design flexibility, process flexibility, & environmental friendliness. Table 2 shows that the multilayer sheets in olefinic Examples 2-6 display the best overall durability performance in comparison to competitive designs. The comparative example of a polyolefin material with block copolymer base and no slip additive is prospective based on known polypropylene examples with no additives.

• 	TABLE 1
  	Olefinic
  	Examples	Iono-	Acrylic/	Solvent	Painted	Painted
  	2-6	mer	ABS	Cast	Plastic	Metal

  Paint	Yes	Yes	Yes	No	No	No
  Free/
  Recyclable
  No Adhesive	Yes	No	Yes	No	No	No
  Between Color
  & Backing
  Layers
  Can Be	Yes	Yes	No	No	No	No
  Laminated or
  Directly
  Formed
  Can Be Used	Yes	Yes	No	Yes	No	No
  as a Tape
  Product
  Can Coextrude	Yes	Yes	Yes	No	No	No
  the Entire
  Structure from
  Thin to Thick
  Sheet With No
  Change in
  Tooling
  Color retention	Pass	Pass	Pass	Fail	Fail	Fail
  vs. percent
  elongation (1.0
  delta E max @
  60%)

• TABLE 2
  				Prospective
  				Comparative
  				Example		Acrylic/
  				Olefin		ABS or
  				w/block		Acrylic/	Solvent
  			Olefinic	copolymer		ASA or	Cast
  		Pass/Fail	Examples	base and no		PC/ASA	Fluoro-	Painted	Painted
  Test	Standard	Criteria	2-6	slip additive	Ionomer	or PC	Acrylic	Plastic	Metal
  Imprint	Honda #16	No Imprint,	Pass	Pass	Fail	Pass	Pass	Pass	Pass
  Resistance		No
  @ 70° C.		Adhesion
  Oil	GM9533P	Compare to	Pass	Pass	Fail	Pass	Pass	Pass (8)	Pass
  Resistance		Control	(8-10)		(4)	(10)	(10)		(8)
  @ 70° C.
  Grease	GM9533P	Compare to	Pass	Pass	Fail	Pass	Pass	Fail (6)	Fail
  Resistance		Control	(8-10)		(4)	(10)	(10)		(6)
  @ 70° C.
  Egg	GM9533P	Compare to	Pass	Pass	Fail	Pass	Fail	Pass (8)	Fail (6)
  Albumin		Control	(10)		(4)	(10)	(6-8)
  Resistance
  @ 70° C.
  Methanol	GM9509P	1	Pass	Pass	Pass	Pass	Pass	Pass	Pass
  Resistance		maximum
  @ RT
  Scratch &	GMW3943	Compare to	Pass	Fail	Pass	Fail	Pass	Pass	Pass
  Mar		Control
  Resistance
  Gravelometer	GM9508P	7 or greater	9	Fail	9	Fails	<7	<7	<7
  	5 pints/					(cracks)
  	90°
  	Impact
  	angle/
  	−30° C.
  Gravelometer	GM9508P	7 or greater	9	Fail	7 but	Fails	<7	<7	<7
  	10 pints/				failed	(cracks)
  	30°				due to
  	degree				delamination
  	impact
  	angle/
  	−30° C.
  Low Temp	GM 9904P	All ductile	Pass	Pass	Pass	Fail	Fail	Fail	Pass
  Impact	GMP.E/P.	failures				shatters
  	148	@ −30° C.
  Crock Mar	CLP 463	Compare to	Pass	Fail	Fail	Fail	Pass	Pass	Pass
  	PB-54	Control
  GM9533P Scale: 10 = no change, 8 = Slight, 6 = Moderate, 4 = Pronounced, 2 = Severe
  GM9509P Scale: 0 = no change, 1 = Slight, 3 = Moderate, 5 = Severe
  GM9508P Scale: 0 = Fail, 1 = Poor−, 2 = Poor, 3 = Poor+, 4 = Fair−, 5 = Fair, 6 = Fair+, 7 = Good−, 8 = Good, 9 = Good+, 10 = no damage/no chipping
  GMW3943 Scale: 1 = no scratch, 2, 3, 4, 5 = Worst
  The test standards used above are available from General Motors, Honda, and Chrysler. Testing was performed by Ghesquire Plastic Testing, Inc. of Harper Woods, MI and A. Schulman Invision of Sharon Center, OH.

• In summary, the favorable results for the example olefinic multilayer structures shown in both tables were made without sacrificing the high gloss and DOI requirements that are needed in order to achieve a Class “A” surface.
Examples 1A-8A
• Examples 1A-8A illustrate the unexpected results obtained by using a multi-layered virgin/regrind/virgin backing layer instead of a blended regrind and virgin monolayer backing layer.FIG. 10 shows anABA backing layer90 that corresponds to Examples 1A-4A.FIG. 10 also shows amonolayer backing layer100 that corresponds to Examples 5A-8A. Bothstructures90,100 were 100 mils in thickness in all the Examples 1A-8A.
• Example 1A is a control showing a single A layer that is not blended with regrind.
• In Examples 2A-4A, the A layers are coextruded with the B layer adjacent to them. The A layer is composed of the materials as specified in Table 3. Percentages are given in weight percents. Though fillers, colorants, stabilizers and other additives are present, the polymeric base is 100% virgin polymer. The B layer is composed of regrind miscellaneous polypropylene homo- and copolymers with talc, filler, colorants, and stabilizers. The polymeric base of the B layer is 100% regrind polymer. Examples 1A-4A vary in the thickness of the A layers and the B layers. In Examples 2A-4A the two A layers in each Example are of equal thicknesses, in values of 40 mil, 30 mil, and 20 mil, respectively.
• In Examples 5A-7A regrind is blended with the virgin polymer and other additives in the amounts disclosed in Table 4. Example 8A is a control using 100% regrind. The same type of regrind material was used in Examples 5A-8A as was used in Examples 2A-4A. The structure in Examples 5A-8A is a single-layer extruded sheet.

• 	TABLE 3
  	Example

  1A

  2A

  3A

  	4A

  A/B/A Layer Thicknesses

  Total A Layer thickness (mils)	100	80.0	60.0	40.0
  B Layer thickness (mils)	0.00	20.0	40.0	60.0

  A Layer Composition

  Pro-Fax 7823 PP (%)	64.301	64.301	64.301	64.301
  DFDB 1088 NT VLDPE (%)	7.920	7.920	7.920	7.920
  Premium HTP Ultra 5L	25.245	25.245	25.245	25.245
  (talc filler) (%)
  TR016 wax	0.594	0.594	0.594	0.594
  (process aid & dispersing aid) (%)
  Chimassorb 119 (UV stabilizer)	0.297	0.297	0.297	0.297
  (%)
  Synpro 12B Calcium Stearate	0.049	0.049	0.049	0.049
  (process aid & dispersing aid) (%)
  Evanstab 18 DSTDP (Evans	0.198	0.198	0.198	0.198
  Chemetics) (antioxidant)
  Irganox B225 (CIBA) (antioxidant)	0.396	0.396	0.396	0.396
  (%)
  Polyblak 3123B (A. Schulman)	1.000	1.000	1.000	1.000
  (black color concentrate) (%)

• 	TABLE 4
  	Example

  5A

  6A

  7A

  	8A

  Total Mono Layer thickness (mils)	100	100	100	100
  Mono-Layer Composition
  Pro-Fax 7823 PP (%)	51.440	38.580	25.720	0.000
  DFDB 1088 NT VLDPE (%)	6.336	4.752	3.168	0.000
  Premium HTP Ultra 5L (talc filler)	20.196	15.147	10.098	0.000
  (%)
  TR016 wax (process aid &	0.475	0.356	0.238	0.000
  dispersing aid) (%)
  Chimassorb 119 (UV stabilizer)	0.238	0.178	0.119	0.000
  (%)
  Synpro 12B Calcium Stearate	0.040	0.030	0.020	0.000
  (process aid & dispersing aid) (%)
  Evanstab 18 DSTDP (antioxidant)	0.158	0.119	0.079	0.000
  Irganox B225 (antioxidant) (%)	0.317	0.238	0.158	0.000
  Polyblak 3123B (black color	1.000	1.000	1.000	1.000
  concentrate) (%)
  Regrind (%)	19.800	39.600	59.400	99.000

• The A layers of Examples 1A-4A were made by the following process. The Pro-Fax 7823 polypropylene and the DFDB 1088NT very low density polyethylene were fed into a Farrell Continuous Mixer. Talc and the other additives listed in Tables 3 were also added. The product of the mixer was natural TPO in pellet form. In the next step, pelletized black color concentrate and the natural TPO pellets were added to a single screw extruder.
• The mono-layer Example 1A was the product of extruding the A layer as a mono-layer sheet.
• The B layers of Examples 2A-4A were made by feeding pelletized and ground up regrind to a single screw extruder.
• In Examples 2A-4A, the extruders were positioned so that each layer would be coextruded in a multilayer stack.
• In Examples 5A-7A Pro-Fax 7823 polypropylene and the DFDB 1088NT very low density polyethylene were fed to a Farrell Continuous Mixer. Talc and the other additives listed in Table 4 were also added. The product of the mixer was a virgin TPO in pellet form. In the next step, pelletized black color concentrate, the virgin TPO pellets, and regrind were added to a single screw extruder and extruded as a mono-layer sheet.
• Example 8A was made by the same process as Examples 4A-7A, except no virgin polymer “Pro-Fax 7823 polypropylene” was added.
Results
• FIG. 11 compares the virgin backing layer of Example 1 and the virgin/regrind/virgin ABA structured backing layers of Examples 2A-4A to the mono-layer structured backing layers of Examples 5A-8A. In particular,FIG. 11 shows the impact of varying amounts of regrind on sag resistance for each type of structure. In these Examples, sag resistance was measured in terms of “bag time,” which is the amount of time required to reach a bag depth of seven inches after heating of the sheet is initiated. The sheet sample size was 40 inches by 20 inches. The sample was heated at 340° F. on a thermoformer. As the data shows, the “bag time” decreases (decreasing sag resistance) as the % regrind increases in both sets of Examples. However, Examples 2A to 4A show improved sag resistance versus Examples 5A to 7A. For example, improvements of 3.5% or greater in terms of time to bag, such as 5% and greater are exhibited by Examples 2A to 4A over Examples 5A to 7A.
• In addition, other properties of the ABA structured backing layer show unexpected improvement compared to the blended mono-layer structure. Table 5 summarizes the results of additional testing performed on Examples 1A-8A. The columns are offset so that Examples that are directly comparative in terms of regrind percentage are in vertical alignment.

• 	TABLE 5
  	Example

  1A

  2A

  3A

  	4A
  	Flex Mod (MPa)	2520	2612	2559	2391
  	% Elong @ Break	327	311	251	199
  	Tensile @ Yield (MPa)	19	19.3	19.8	21
  	Ductile/Brittle Pt (° C.)	−20	−20	−20	−10
  	Energy to Max Load (J)	29	29	31	29
  	Total Energy (J)	49	49	51	49

  Example

  5A

  6A

  7A

  	8A
  	Flex Mod (MPa)	2474	2278	2030	1278
  	% Elong @ Break	325	251	264	33
  	Tensile @ Yield (Mpa)	19	19	20	19
  	Ductile/Brittle Pt (° C.)	−10	−10	−10	brittle
  					@ 0
  	Energy to Max Load (J)	30	30	31	3
  	Total Energy (J)	51	49	51	4

• The flexural modulus was tested according ISO 178 at 2 mm/min and a 64 mm span. The elongation at break and tensile at yield parameters were tested according to ISO 527 at 50 mm/min. The ductile/brittle point, energy to Max Load, and total energy measurements were tested according to GM9904P at 2.2 m/s. For the flexural modulus, percent elongation at break, and tensile at yield tests, the samples were cut parallel to the direction of the extrusion flow.
• This written description sets forth the best mode of the invention, and describes the invention so as to enable a person skilled in the art to make and use the invention, by presenting examples. The patentable scope of the invention is defined by the claims, and may include other examples that occur to those skilled in the art.

Claims (18)

1. A multilayer structure comprising:

a first thermoplastic layer having a polymeric component consisting essentially of virgin polyolefin;

a second thermoplastic layer including regrind polyolefin; and

a third thermoplastic layer having a polymeric component consisting essentially of virgin polyolefin;

the second thermoplastic layer being adjacent to the first thermoplastic layer and the third thermoplastic layer.

2. The multilayer structure ofclaim 1 wherein the multilayer structure includes a clear polymer layer.

3. The multilayer structure ofclaim 1 wherein the polymeric component of the second layer consists essentially of regrind.

4. The multilayer structure ofclaim 3 wherein the bag strength of the first, second, and third layer is at least 5% greater than a control sample that is identical to the first, second, and third layer in formulation and dimension, but has a mono-layer structure that incorporates a blend of the regrind and the virgin polymer instead of a multi-layered structure.

5. The multilayer structure ofclaim 2 wherein the multilayer structure further comprises a colored polymeric layer adjacent to the clear layer.

6. The multilayer structure ofclaim 1 wherein the virgin polyolefin comprises a propylene homopolymer or a copolymer including polypropylene, and further comprises a very low density polyethylene.

7. A backing layer for a multilayered polymeric structure comprising:

a first thermoplastic layer including a polymeric component, wherein the polymeric component consists essentially of a virgin polyolefin;

a second thermoplastic layer including regrind polyolefin;

a third thermoplastic layer having a polymeric component, wherein the polymeric component consists essentially of a virgin polyolefin;

the second thermoplastic layer being adjacent to the first thermoplastic layer and the third thermoplastic layer, if present.

8. The backing layer ofclaim 7 wherein the polymeric component of the second layer consists essentially of regrind.

9. The backing layer ofclaim 7 wherein the bag strength of the backing layer is at least 3% higher in terms of the time to bag, than a control sample that is identical to the backing layer in formulation and dimension, but has a mono-layer structure that incorporates a blend of the regrind and the virgin polymer instead of a multi-layered structure.

10. The backing layer ofclaim 7 wherein the virgin polyolefin comprises a propylene homopolymer or a copolymer including polypropylene, and further comprises a very low density polyethylene.

11. A method for forming a multilayered polymeric structure, the method comprising coextruding a first thermoplastic layer having a polymeric component that consists essentially of a virgin polyolefin, with a second thermoplastic layer including regrind polyolefin, and a third thermoplastic layer having a polymeric component that consists essentially of a virgin polyolefin;

the second thermoplastic layer being adjacent to the first thermoplastic layer and the third thermoplastic layer.

12. The method ofclaim 11 wherein the coextrusion step further comprises coextruding a clear polymeric layer with the first, second, and third thermoplastic layers.

13. The method ofclaim 11 wherein the coextrusion step further comprises coextruding a clear polymeric layer and a colored polymeric layer with the first, second, and third thermoplastic layers.

14. The method ofclaim 11 further comprising thermoforming the coextruded multilayered polymeric structure to make a formed product.

15. The method ofclaim 11 wherein the polymeric component of the second layer consists essentially of regrind.

16. The method ofclaim 11 wherein the virgin polyolefin comprises a propylene homopolymer or a copolymer including polypropylene, and further comprises a very low density polyethylene.

17. The method claim of11 wherein the formed product is a backing layer for a vehicle body panel.

18. The method ofclaim 11 wherein the bag strength of the multilayered polymeric structure after coextrusion is at least 3% higher in terms of the time to bag, than a control sample that is identical to the backing layer in formulation and dimension but has a mono-layer structure that incorporates a blend of the regrind and the virgin polymer instead of a multi-layered structure.

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