USH1274H - Polypropylene-polybutylene heat sealable laminated packaging film with improved optics - Google Patents
Polypropylene-polybutylene heat sealable laminated packaging film with improved optics Download PDFInfo
- Publication number
- USH1274H USH1274H US07/677,049 US67704991A USH1274H US H1274 H USH1274 H US H1274H US 67704991 A US67704991 A US 67704991A US H1274 H USH1274 H US H1274H
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- United States
- Prior art keywords
- melt index
- weight
- propylene
- film
- core
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 229920001748 polybutylene Polymers 0.000 title claims description 11
- 229920006280 packaging film Polymers 0.000 title abstract description 3
- 239000012785 packaging film Substances 0.000 title abstract description 3
- -1 polypropylene Polymers 0.000 claims abstract description 33
- 229920001519 homopolymer Polymers 0.000 claims abstract description 20
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims abstract description 18
- 229920005604 random copolymer Polymers 0.000 claims abstract description 14
- 239000012792 core layer Substances 0.000 claims abstract description 8
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims abstract 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 44
- 239000010410 layer Substances 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 21
- 239000000155 melt Substances 0.000 claims description 20
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 12
- 239000005977 Ethylene Substances 0.000 claims description 12
- 229920000642 polymer Polymers 0.000 claims description 7
- 229920001384 propylene homopolymer Polymers 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 239000004711 α-olefin Substances 0.000 claims description 5
- 239000002365 multiple layer Substances 0.000 claims 3
- 229920005606 polypropylene copolymer Polymers 0.000 claims 3
- 239000004743 Polypropylene Substances 0.000 abstract description 20
- 229920001155 polypropylene Polymers 0.000 abstract description 17
- 239000002344 surface layer Substances 0.000 abstract description 4
- 229920005630 polypropylene random copolymer Polymers 0.000 description 14
- 229920001577 copolymer Polymers 0.000 description 12
- 239000011162 core material Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 230000003287 optical effect Effects 0.000 description 9
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 8
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 7
- 238000002156 mixing Methods 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 229910010062 TiCl3 Inorganic materials 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- 229920001038 ethylene copolymer Polymers 0.000 description 2
- 238000007765 extrusion coating Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 description 2
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000007630 basic procedure Methods 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 229920005629 polypropylene homopolymer Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2323/00—Polyalkenes
- B32B2323/10—Polypropylene
Definitions
- the invention relates to a multi-layer, thermoplastic heat-sealable film suitable for conventional heat sealable packaging applications.
- Polypropylene film has become a useful and widely accepted packaging film because of its good moisture barrier, stiffness, high strength, and good optical properties.
- the optical properties of polypropylene films in certain applications are sometimes critical and improvement has long been needed.
- U.S. Pat. No. 4,230,767 discloses a laminated packaging material with heat seal packaging properties composed of a polypropylene base layer and a surface layer of a two component blend of a propylene/ethylene copolymer with a variety of other olefins and copolymers including polybutylene copolymers.
- U.S. Pat. No. 4,230,767 does not disclose the use of a high melt index polybutylene in a laminated film with a polypropylene core.
- U.S. Ser. No. 531,206, filed May 31, 1990 now U.S. Pat. No. 5,073,458 discloses a laminated film having a polypropylene core which is coated with layers of a blend of polypropylene random copolymer and a high melt index poly-1-butene. Applicant has found that a laminate having a polypropylene core and polypropylene random copolymer outer layers gives films having surprisingly better optical properties when a minor amount of a high melt index poly-1-butene is added either to the core or to the outer layers.
- the present invention is a novel multi-layer film composition having an unexpected combination of high tear strength, good processability, and improved optics.
- the film comprises a "core" or substrate of propylene homopolymer or copolymer or blends of propylene polymer with butene-1 homopolymers and copolymers.
- This core is coated on one or both sides with a propylene/ethylene random copolymer composition or a blend comprising a propylene/ethylene random copolymer and a low melt index butylene homopolymer or low melt index butylene/ethylene copolymer wherein a minor amount of a high melt index butylene homopolymer is blended with the core or the outer layer composition.
- the film may be made by any conventional technique in which a skin layer, which is substantially an ethylene/propylene copolymer blend, may be applied to a core or base layer consisting substantially of polypropylene. Any of the known methods of coextrusion or of extrusion coating can be used to make this film.
- the film-forming composition, or any component thereof, can be used unaltered or can be modified with additives for improvement of slip, antiblock or static properties of the finished film.
- Resins useful for the core layer of the present invention include low melt index propylene homopolymers and copolymers.
- the outer skin material may comprise a blend of a propylene/ethylene random copolymer optionally with a butene-1 homopolymer or copolymer and a minor amount of high melt index poly-1-butene homopolymer.
- the polypropylene used in the present invention is any crystallizable polypropylene.
- Said polypropylene can be prepared by polymerizing propylene irrespective of the method used so long as crystallizable polypropylene is formed.
- the preferred polypropylenes are the substantially isotactic polypropylenes prepared by the Ziegler/Natta or MgCl 2 -supported catalyst polymerization process.
- the propylene polymers usable in the core layer can be either propylene homopolymers or copolymers. If propylene copolymers are used, they can be random or block copolymers with the comomoner content preferably 1-30 mole % of either ethylene, butene, or an alpha olefin having from 5 to 8 carbon atoms.
- Propylene polymers useful for the core layer in the invention preferably have a melt index of less than 60, more preferably from about 1-15, as measured by ASTM D-1238, Condition L at 230° C.
- a particularly suitable propylene has a melt index of 2.6 and is available from Shell Chemical Company, of Houston, Tex. as PP5A08.
- the outer skin layers comprise a blend of a propylene-ethylene random copolymer, and optionally a low melt index butene-1 polymer and a high melt index butene-1 homopolymer.
- the propylene-ethylene random copolymers have an ethylene content of 7% by weight or less and have a melting point of 130° C. or higher or preferably 150° C. or higher and a melt index of from 2 to 20 g/10 minutes, preferably 4 to 15 g/10 minutes, most preferably 6 to 10 g/10 minutes as measured by ASTM D-1238, Condition L at 230° C.
- the low melt index butene-1 polymers referred to herein are substantially poly-1-butene homopolymers or copolymers containing at least 95%, preferably 97%, and most preferably 98% by weight of isotactic portions. Suitable poly-1-butenes have a density of 0.895-0.919.
- Suitable poly-1-butenes can be obtained, for example, according to Ziegler-Natta low pressure polymerization of butene-1 as disclosed in German Published Application No. 1,570,353.
- the butene-1 polymers usable in the outer layers are either butene-1 homopolymers or copolymers. If butene-1 copolymers are used, the non-butene comonomer content can be 0.1-20 mole % preferably 0.2-10 mole % or more preferably 0.3-6 mole % of either ethylene, propylene, or an alpha olefin having from 5 to 8 carbon atoms.
- Suitable poly-1-butenes can be obtained, for example, in accordance with Ziegler-Natta low-pressure polymerization of butene-1, e.g. by polymerizing butene-1 with catalysts of TiCl 3 or TiCl 3 .AlCl 3 and Al(C 2 H 5 ) 2 Cl at temperatures of 10°-50° C., preferably 20°-40° C., e.g. according to the process of German Published Application No. 1,570,353. High melt indices are then obtained by further processing the polymer by peroxide cracking.
- the poly-1-butenes may be modified to increase surface activity by reaction with, for example, maleic anhydride or other functional group.
- the high melt index poly-1-butene referred to herein is a butene-1 polymer containing at least about 90%, preferably at least about 95%, and more preferably about 97%, by weight of isotactic portions.
- isotactic poly-1-butenes having a low molecular weight, e.g. less than about 280,000 as determined by solution viscosity in "Decalin” (decahydronophthalene).
- Usable poly-1-butenes have a density of 0.895-0.925, preferably 0.905-0.920 and especially 0.910-0.915.
- Usable poly-1-butenes have melt indices in the range of from 20 to 1000, more preferably 30-650, more preferably 50-500, and most preferably 100-300 g/10 min. as determined by ASTM D-1238 Condition E, at 190° C.
- the intrinsic viscosity of the polybutylene may range from about 0.03 to about 0.20 preferably from about 0.06 to about 0.11 at 130° C.
- the Brookfield melt viscosity of the high melt index polybutylene may range from about 10,000 to about 200,000 centipoise, preferably 25,000 to 150,000 centipoise and most preferably from 40,000 to 100,000 centipoise at 200° C.
- the laminate compositions may also contain additives and fillers, e.g. mold release agents, UV or thermal stabilizers, slip agents, antiblock agents, nucleating agents, pigments, antioxidants, or flame retardants.
- additives and fillers e.g. mold release agents, UV or thermal stabilizers, slip agents, antiblock agents, nucleating agents, pigments, antioxidants, or flame retardants.
- Blending of the components can occur by one of several methods, dry tumble blending, masterbatch, or melt compounding techniques.
- the method of combining the ingredients of the formulation is important. For example, in most cases, it is desirable to use the least amount of energy to merge the components into an effective blend. Therefore, the preferred method of blending is dry blending the components in a powder form.
- the coated thermoplastic film of the present invention may be formed by any conventional technique for producing a multi-layered film, for example: coextrusion, lamination of previously extruded films; extrusion coating; emulsion coating; and so forth.
- the preferred method is coextrusion, but it is not our intention to limit the means of production to any single technique.
- the skin layer of the laminate structure embodied herein is usually 0.02 mil to 0.8 mil for every mil of total film thickness. Generally preferred is a skin of 0.05 mil to 0.6 mil and a total film thickness of 0.5 mil to 2.0 mils.
- the coating or skin may comprise from 3% to 30% of the total thickness of the laminated film.
- Films were prepared by coextruding a core material of polypropylene homopolymer or polypropylene hompolymer blended with high melt index poly-1-butene with a coating on both sides thereof comprising a polypropylene random copolymer alone (control) or blends with other components as shown in Table I.
- the molten polymers were coextruded from a conventional extruder through a flat 10" sheet die, the melt streams being combined in an adaptor prior to being extruded from the die.
- Each skin layer comprised approximately 1/3 of the total thickness of the film.
- the resin was extruded at about 230° C. for the skin material and 225° C. for the core material and 235° C. for the die.
- the coated sheets (about 18 mils in thickness) were rolled on a chilled roll at about 10° C. (50° F). The sheets were then trimmed and wound on cores. The sheets were then stretched by a biaxial film stretcher with 6 times in one direction and 5 times in the other direction.
- PPR is propylene random copolymer with an ethylene content of 5 wt % and a melt index of 8.0 available from Solvey as KS409.
- PP is propylene homopolymer with a melt index of 2.2 g/10 min. at 230° C. and a density of 0.905, available from U.S. Steel Corp. as FF020Y.
- PB8340 is a poly-1-butene copolymer with ethylene comonomer content of 0.75 wt % and a melt index of 4.0 g/10 min. at 190° C. and a molecular weight of 325,000 available from Shell Chemical Company, Houston, Tex.
- DP0800 is a high melt index butene-1 homopolymer with a melt index of 200 g/10 min. at 190° C., molecular weight of 108,000, available from Shell Chemical Company, Houston, Tex.
- Tables III and IV show the optical properties for the six sample films.
- Table III shows optical properties including gloss measured at an angle of 60°.
- Table IV shows optical properties including gloss, measured at an angle of 45°, of a second set of similarly prepared films. Films with surface layers, or a core layer, containing a minor amount of high melt index poly-1-butene, compositions 2, 3, 5 and 6, were processed very easily and had no handling problems since the surface was not tacky.
- the laminated films of the present invention i.e. Films 2, 3, 5 and 6 have significantly better optical properties than the control films 1 and 4 and do not have any problems associated with a tacky surface.
Landscapes
- Laminated Bodies (AREA)
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
Abstract
A packaging film comprising a core layer of polypropylene and a surface layer comprising a propylene ethylene random copolymer wherein at least one of said core or said surface layers contains a minor amount of a high melt index butylene homopolymer.
Description
1. Field of the Invention
The invention relates to a multi-layer, thermoplastic heat-sealable film suitable for conventional heat sealable packaging applications.
2. Brief Description of the Prior Art
Polypropylene film has become a useful and widely accepted packaging film because of its good moisture barrier, stiffness, high strength, and good optical properties. However, the optical properties of polypropylene films in certain applications are sometimes critical and improvement has long been needed.
U.S. Pat. No. 4,230,767 discloses a laminated packaging material with heat seal packaging properties composed of a polypropylene base layer and a surface layer of a two component blend of a propylene/ethylene copolymer with a variety of other olefins and copolymers including polybutylene copolymers. U.S. Pat. No. 4,230,767 does not disclose the use of a high melt index polybutylene in a laminated film with a polypropylene core.
U.S. Pat. Nos. 4,681,804; 4,677,025; 4,769,421; 4,343,852; and 4,766,178 disclose laminated films containing polypropylene and polybutylene, however none disclose the use of high melt index polybutylene as presently claimed.
U.S. Ser. No. 531,206, filed May 31, 1990 now U.S. Pat. No. 5,073,458 discloses a laminated film having a polypropylene core which is coated with layers of a blend of polypropylene random copolymer and a high melt index poly-1-butene. Applicant has found that a laminate having a polypropylene core and polypropylene random copolymer outer layers gives films having surprisingly better optical properties when a minor amount of a high melt index poly-1-butene is added either to the core or to the outer layers.
The present invention is a novel multi-layer film composition having an unexpected combination of high tear strength, good processability, and improved optics. The film comprises a "core" or substrate of propylene homopolymer or copolymer or blends of propylene polymer with butene-1 homopolymers and copolymers. This core is coated on one or both sides with a propylene/ethylene random copolymer composition or a blend comprising a propylene/ethylene random copolymer and a low melt index butylene homopolymer or low melt index butylene/ethylene copolymer wherein a minor amount of a high melt index butylene homopolymer is blended with the core or the outer layer composition.
The film may be made by any conventional technique in which a skin layer, which is substantially an ethylene/propylene copolymer blend, may be applied to a core or base layer consisting substantially of polypropylene. Any of the known methods of coextrusion or of extrusion coating can be used to make this film.
The film-forming composition, or any component thereof, can be used unaltered or can be modified with additives for improvement of slip, antiblock or static properties of the finished film.
Resins useful for the core layer of the present invention include low melt index propylene homopolymers and copolymers. The outer skin material may comprise a blend of a propylene/ethylene random copolymer optionally with a butene-1 homopolymer or copolymer and a minor amount of high melt index poly-1-butene homopolymer.
The polypropylene used in the present invention is any crystallizable polypropylene. Said polypropylene can be prepared by polymerizing propylene irrespective of the method used so long as crystallizable polypropylene is formed. The preferred polypropylenes are the substantially isotactic polypropylenes prepared by the Ziegler/Natta or MgCl2 -supported catalyst polymerization process.
The propylene polymers usable in the core layer can be either propylene homopolymers or copolymers. If propylene copolymers are used, they can be random or block copolymers with the comomoner content preferably 1-30 mole % of either ethylene, butene, or an alpha olefin having from 5 to 8 carbon atoms.
Propylene polymers useful for the core layer in the invention preferably have a melt index of less than 60, more preferably from about 1-15, as measured by ASTM D-1238, Condition L at 230° C. A particularly suitable propylene, has a melt index of 2.6 and is available from Shell Chemical Company, of Houston, Tex. as PP5A08.
The outer skin layers comprise a blend of a propylene-ethylene random copolymer, and optionally a low melt index butene-1 polymer and a high melt index butene-1 homopolymer.
The propylene-ethylene random copolymers have an ethylene content of 7% by weight or less and have a melting point of 130° C. or higher or preferably 150° C. or higher and a melt index of from 2 to 20 g/10 minutes, preferably 4 to 15 g/10 minutes, most preferably 6 to 10 g/10 minutes as measured by ASTM D-1238, Condition L at 230° C.
The low melt index butene-1 polymers referred to herein are substantially poly-1-butene homopolymers or copolymers containing at least 95%, preferably 97%, and most preferably 98% by weight of isotactic portions. Suitable poly-1-butenes have a density of 0.895-0.919.
Suitable poly-1-butenes can be obtained, for example, according to Ziegler-Natta low pressure polymerization of butene-1 as disclosed in German Published Application No. 1,570,353.
The butene-1 polymers usable in the outer layers are either butene-1 homopolymers or copolymers. If butene-1 copolymers are used, the non-butene comonomer content can be 0.1-20 mole % preferably 0.2-10 mole % or more preferably 0.3-6 mole % of either ethylene, propylene, or an alpha olefin having from 5 to 8 carbon atoms.
Suitable poly-1-butenes can be obtained, for example, in accordance with Ziegler-Natta low-pressure polymerization of butene-1, e.g. by polymerizing butene-1 with catalysts of TiCl3 or TiCl3.AlCl3 and Al(C2 H5)2 Cl at temperatures of 10°-50° C., preferably 20°-40° C., e.g. according to the process of German Published Application No. 1,570,353. High melt indices are then obtained by further processing the polymer by peroxide cracking. The poly-1-butenes may be modified to increase surface activity by reaction with, for example, maleic anhydride or other functional group.
The high melt index poly-1-butene referred to herein is a butene-1 polymer containing at least about 90%, preferably at least about 95%, and more preferably about 97%, by weight of isotactic portions. Useful in the present invention are isotactic poly-1-butenes having a low molecular weight, e.g. less than about 280,000 as determined by solution viscosity in "Decalin" (decahydronophthalene). Usable poly-1-butenes have a density of 0.895-0.925, preferably 0.905-0.920 and especially 0.910-0.915. Usable poly-1-butenes have melt indices in the range of from 20 to 1000, more preferably 30-650, more preferably 50-500, and most preferably 100-300 g/10 min. as determined by ASTM D-1238 Condition E, at 190° C. The intrinsic viscosity of the polybutylene may range from about 0.03 to about 0.20 preferably from about 0.06 to about 0.11 at 130° C. The Brookfield melt viscosity of the high melt index polybutylene may range from about 10,000 to about 200,000 centipoise, preferably 25,000 to 150,000 centipoise and most preferably from 40,000 to 100,000 centipoise at 200° C.
The laminate compositions may also contain additives and fillers, e.g. mold release agents, UV or thermal stabilizers, slip agents, antiblock agents, nucleating agents, pigments, antioxidants, or flame retardants.
Blending of the components can occur by one of several methods, dry tumble blending, masterbatch, or melt compounding techniques. The method of combining the ingredients of the formulation is important. For example, in most cases, it is desirable to use the least amount of energy to merge the components into an effective blend. Therefore, the preferred method of blending is dry blending the components in a powder form.
The coated thermoplastic film of the present invention may be formed by any conventional technique for producing a multi-layered film, for example: coextrusion, lamination of previously extruded films; extrusion coating; emulsion coating; and so forth. The preferred method is coextrusion, but it is not our intention to limit the means of production to any single technique.
The skin layer of the laminate structure embodied herein is usually 0.02 mil to 0.8 mil for every mil of total film thickness. Generally preferred is a skin of 0.05 mil to 0.6 mil and a total film thickness of 0.5 mil to 2.0 mils. The coating or skin may comprise from 3% to 30% of the total thickness of the laminated film.
The following Examples illustrate the invention but are not to be considered as limiting it.
Films were prepared by coextruding a core material of polypropylene homopolymer or polypropylene hompolymer blended with high melt index poly-1-butene with a coating on both sides thereof comprising a polypropylene random copolymer alone (control) or blends with other components as shown in Table I. The molten polymers were coextruded from a conventional extruder through a flat 10" sheet die, the melt streams being combined in an adaptor prior to being extruded from the die. Each skin layer comprised approximately 1/3 of the total thickness of the film. The resin was extruded at about 230° C. for the skin material and 225° C. for the core material and 235° C. for the die.
After leaving the die orifice, the coated sheets (about 18 mils in thickness) were rolled on a chilled roll at about 10° C. (50° F). The sheets were then trimmed and wound on cores. The sheets were then stretched by a biaxial film stretcher with 6 times in one direction and 5 times in the other direction.
Using this same basic procedure, films were prepared having the following compositions:
TABLE I
__________________________________________________________________________
FILM STRUCTURE
# Skin Core Skin
__________________________________________________________________________
PPR PP PPR CONTROL
PPR PP + 3% DP0800
PPR
PPR + 3% PB0B00 PP PPR + 3% DP0800
PPR + 40% PB8340 PP PPR + 40% PB8340 CONTROL
PPR + 40% PB8340 PP + 3% DP0800
PPR + 40% PB8340
PPR + 40% PB8340 + 3% DP0800
PP PPR + 40% PB8340 + 3% DP0800
__________________________________________________________________________
The various materials used for the example films were as follows:
PPR is propylene random copolymer with an ethylene content of 5 wt % and a melt index of 8.0 available from Solvey as KS409.
PP is propylene homopolymer with a melt index of 2.2 g/10 min. at 230° C. and a density of 0.905, available from U.S. Steel Corp. as FF020Y.
PB8340 is a poly-1-butene copolymer with ethylene comonomer content of 0.75 wt % and a melt index of 4.0 g/10 min. at 190° C. and a molecular weight of 325,000 available from Shell Chemical Company, Houston, Tex.
DP0800 is a high melt index butene-1 homopolymer with a melt index of 200 g/10 min. at 190° C., molecular weight of 108,000, available from Shell Chemical Company, Houston, Tex.
The typical physical properties of the high melt index polybutylene (DP0800) are listed below in Table II.
TABLE II
__________________________________________________________________________
Typical Physical Properties of DP0800 Polybutylene
Unit
ASTM Test Method
English
(Metric)
Polybutylene DP0800
__________________________________________________________________________
Melt Index
@ 190° C.
D1238 "E" -- g/10 min
200
@ 230° C.
D1238 "L" -- g/10 min
490
Density D1505 lb/ft g/cms 57.1 (0.915)
Tensile strength @ yield
D638 psi MPa 2000 (13.8)
Tensile strength @ break
D638 psi MPa 4200 (29.0)
Elongation at break
D638 % % 350
Modulus of elasticity
D638 psi MPa 35000 (241)
Hardness, Shore
D2240 D scale
D scale
55 (55)
Brittleness temperature
D746 °F.
°C.
0° (-18°)
Melting point range
DSC °F.
°C.
255-259°
(124-126°)
Soft point, Vicat
D1525 °F.
°C.
241° (116°)
Thermal conductivity,
C177 Btu/ft.sup.2 /
Kcal/m.sup.2
1.25
at 77° F. hr/°F./in
hr/°C./cm
(16)
Melt Viscosity at 200° C.
Brookfield
centipoise
-- 3.9 × 10.sup.4
__________________________________________________________________________
Tables III and IV show the optical properties for the six sample films. Table III shows optical properties including gloss measured at an angle of 60°. Table IV shows optical properties including gloss, measured at an angle of 45°, of a second set of similarly prepared films. Films with surface layers, or a core layer, containing a minor amount of high melt index poly-1-butene, compositions 2, 3, 5 and 6, were processed very easily and had no handling problems since the surface was not tacky.
TABLE III
______________________________________
OPTICAL PROPERTIES
THICKNESS HAZE GLOSS
FILM COMPOSITION
MICRONS % (@ 60°)
______________________________________
1. Control 13 0.4 113.1
2. 27.5 0.2 127.1
3. 15.5 0.2 130.0
4. Control 15.5 0.4 111.3
5. 24.5 0.3 136.5
6. 15.5 0.4 131.1
______________________________________
TABLE IV
______________________________________
OPTICAL PROPERTIES
THICKNESS HAZE GLOSS
FILM COMPOSITION
MICRONS % (@ 45°)
______________________________________
1. Control 13 0.5 80.0
2. 27.5 0.39 81.0
3. 15.5 0.43 81.5
4. Control 15.5 1.87 69.5
5. 24.5 0.55 77.0
6. 15.5 0.88 81.0
______________________________________
As can be seen from this data, the laminated films of the present invention, i.e. Films 2, 3, 5 and 6 have significantly better optical properties than the control films 1 and 4 and do not have any problems associated with a tacky surface.
Certain changes in the above description of preparing the polymer blend and film may be made without departing from the scope of this invention and it is intended that all matter contained in this description is interpreted as illustrative and not in a limiting sense.
Claims (12)
1. A multiple-layer, heat-sealable laminated film comprising:
(I) a core layer comprising propylene homopolymer and copolymers of propylene with from 1% to about 30% by weight of an α-olefin having 2 or 4 to 8 carbon atoms,
(II) on at least one side of said core, an outer layer comprising a propylene-ethylene random copolymer having an ethylene content of 7% by weight or less,
wherein at least one of said core or said outer layer contains from about 0.2% to about 10% by weight of a high melt index butene-1 homopolymer having a melt index of from about 20 to about 1000 g/10 minutes at 190° C.
2. The film of claim 1 wherein the high melt index butylene homopolymer has a melt index of from 30 to 650 g/10 minutes at 190° C.
3. The film of claim 1 wherein the high melt index butylene homopolymer has a melt index of from 50 to 300 g/10 minutes at 190° C.
4. The film of claim 1 wherein the high melt index butylene homopolymer has a melt index of from 100 to 200 g/10 minutes at 190° C.
5. The film of claim 1 wherein the high melt index butylene homopolymer has a melt viscosity of from 10,000 to about 200,000 centipoise at 200° C.
6. The film of claim 1 wherein the high melt index butylene homopolymer has a melt viscosity of from 40,000 to 100,000 centipoise at 200° C.
7. The laminated film of claim 1 wherein said outer layer is from about 0.02 mils to about 0.6 mils thick and the total film thickness is between 0.5 and 2.0 mils.
8. The laminated film of claim 1 wherein the film is formed by coextrusion.
9. A multiple-layer, heat-sealable laminated film comprising:
(I) a core layer comprising propylene homopolymers and copolymers of propylene with from 1% to about 30% by weight of an α-olefin having 2, or 4 to 8 carbon atoms,
(II) on at least one side of said core, an outer layer comprising a blend of:
(a) from 40% to 80% by weight of a propylene-ethylene random copolymer having an ethylene content of 7% by weight or less,
(b) from 20% to 60% by weight of a low melt index butene-1 polymer having a melt index of between 1.0 and 15 g/10 minutes at 190° C.,
and wherein at least one of said core or said outer layer contains from about 0.2% to about 10% by weight of a high melt index butene-1 homopolymer having a melt index of from about 20 to about 1000 g/10 minutes at 190° C.
10. The film of claim 9 wherein the outer layer comprises from 50 to 70% by weight of said propylene ethylene random copolymer, 30 to 50% by weight of said low melt index polybutylene and from 0.5 to about 5.0% by weight of said high melt index butylene homopolymer.
11. The film of claim 10 wherein the outer layer comprises from 55 to 65% by weight of said propylene ethylene random copolymer, 35 to 45% by weight of said low melt index polybutylene and from 2.0 to about 4.0% by weight of said high melt index butylene homopolymer.
12. A multiple-layer, heat-sealable laminated film comprising:
(I) a core layer comprising propylene homopolymers and copolymers of propylene with from 1% to about 30% by weight of an α-olefin having 2, or 4 to 8 carbon atoms,
(II) on at least one side of said core, an outer layer comprising a blend of:
(a) from 55% to 65% by weight of a propylene-ethylene random copolymer having an ethylene content of 7% by weight or less, and a melt index of from 6 to 10 g/10 minutes at 230° C.,
(b) from 35% to 45% by weight of a low melt index butene-1 ethylene random copolymer having an ethylene content of from 0.3 to 20.0 mole % and a melt index of between 1.0 and 15 g/10 min. at 190° C.,
wherein at least one of said core or said outer layer contains from about 2% to about 4% by weight of a high melt index butene-1 homopolymer having a melt index of from 100 to about 300 g/10 minutes at 190° C., and a melt viscosity of between 40,000 and 100,000 centipoise at 200° C.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/677,049 USH1274H (en) | 1991-03-29 | 1991-03-29 | Polypropylene-polybutylene heat sealable laminated packaging film with improved optics |
| JP4036913A JPH0564867A (en) | 1991-03-29 | 1992-01-29 | Polypropylene-polybutylene heat sealable laminated packaging film with improved optical properties |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/677,049 USH1274H (en) | 1991-03-29 | 1991-03-29 | Polypropylene-polybutylene heat sealable laminated packaging film with improved optics |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USH1274H true USH1274H (en) | 1994-01-04 |
Family
ID=24717101
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/677,049 Abandoned USH1274H (en) | 1991-03-29 | 1991-03-29 | Polypropylene-polybutylene heat sealable laminated packaging film with improved optics |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | USH1274H (en) |
| JP (1) | JPH0564867A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5733617A (en) * | 1994-03-21 | 1998-03-31 | L'oreal | Packaging made of composite plastic exhibiting a soft feel effect |
| US20030224194A1 (en) * | 2001-03-02 | 2003-12-04 | Uvtech,L.P. | Polymer system for thick polymer sheets including syndiotactic polyoropylene or poly-1-butene |
| US20040146729A1 (en) * | 2003-01-24 | 2004-07-29 | Ahmed Sharf U. | Moisture vapor permeable film including ethylene copolymer and articles including the same |
| US20080017655A1 (en) * | 2006-07-19 | 2008-01-24 | Martel Shelly A | Food container assembly |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4277220B2 (en) | 2005-06-24 | 2009-06-10 | ブラザー工業株式会社 | Image forming apparatus |
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-
1991
- 1991-03-29 US US07/677,049 patent/USH1274H/en not_active Abandoned
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5733617A (en) * | 1994-03-21 | 1998-03-31 | L'oreal | Packaging made of composite plastic exhibiting a soft feel effect |
| US20030224194A1 (en) * | 2001-03-02 | 2003-12-04 | Uvtech,L.P. | Polymer system for thick polymer sheets including syndiotactic polyoropylene or poly-1-butene |
| US20040146729A1 (en) * | 2003-01-24 | 2004-07-29 | Ahmed Sharf U. | Moisture vapor permeable film including ethylene copolymer and articles including the same |
| US7405009B2 (en) | 2003-01-24 | 2008-07-29 | H.B. Fuller Licensing & Financing, Inc. | Moisture vapor permeable film including ethylene copolymer and articles including the same |
| US20080017655A1 (en) * | 2006-07-19 | 2008-01-24 | Martel Shelly A | Food container assembly |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0564867A (en) | 1993-03-19 |
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| AS | Assignment |
Owner name: SHELL OIL COMPANY Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:HWO, CHARLES C.;REEL/FRAME:006296/0611 Effective date: 19910326 |
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