EP0775051A4 - Packaging seal layer - Google Patents

Packaging seal layer

Info

Publication number
EP0775051A4
EP0775051A4 EP95930805A EP95930805A EP0775051A4 EP 0775051 A4 EP0775051 A4 EP 0775051A4 EP 95930805 A EP95930805 A EP 95930805A EP 95930805 A EP95930805 A EP 95930805A EP 0775051 A4 EP0775051 A4 EP 0775051A4
Authority
EP
European Patent Office
Prior art keywords
seal layer
ethylene
carbon monoxide
component
thermoplastic
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.)
Ceased
Application number
EP95930805A
Other languages
German (de)
French (fr)
Other versions
EP0775051A1 (en
Inventor
Karlheinz Hausmann
H Dieter Flieger
Heiko E Schenck
David R Sparrow
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Priority to EP95930805A priority Critical patent/EP0775051A4/en
Publication of EP0775051A1 publication Critical patent/EP0775051A1/en
Publication of EP0775051A4 publication Critical patent/EP0775051A4/en
Ceased legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered 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
    • B32B27/08Layered 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/30Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B32B27/306Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising vinyl acetate or vinyl alcohol (co)polymers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/32Layered products comprising a layer of synthetic resin comprising polyolefins
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B37/00Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
    • B32B37/14Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers
    • B32B37/15Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with at least one layer being manufactured and immediately laminated before reaching its stable state, e.g. in which a layer is extruded and laminated while in semi-molten state
    • B32B37/153Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with at least one layer being manufactured and immediately laminated before reaching its stable state, e.g. in which a layer is extruded and laminated while in semi-molten state at least one layer is extruded and immediately laminated while in semi-molten state
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/04Interconnection of layers
    • B32B7/06Interconnection of layers permitting easy separation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/04Interconnection of layers
    • B32B7/12Interconnection of layers using interposed adhesives or interposed materials with bonding properties
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D75/00Packages comprising articles or materials partially or wholly enclosed in strips, sheets, blanks, tubes, or webs of flexible sheet material, e.g. in folded wrappers
    • B65D75/52Details
    • B65D75/58Opening or contents-removing devices added or incorporated during package manufacture
    • B65D75/5855Peelable seals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L73/00Compositions of macromolecular compounds obtained by reactions forming a linkage containing oxygen or oxygen and carbon in the main chain, not provided for in groups C08L59/00 - C08L71/00; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J123/00Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
    • C09J123/02Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
    • C09J123/04Homopolymers or copolymers of ethene
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2250/00Layers arrangement
    • B32B2250/24All layers being polymeric
    • B32B2250/246All polymers belonging to those covered by groups B32B27/32 and B32B27/30
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2323/00Polyalkenes
    • B32B2323/04Polyethylene
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2331/00Polyvinylesters
    • B32B2331/04Polymers of vinyl acetate, e.g. PVA
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2553/00Packaging equipment or accessories not otherwise provided for
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02Organic macromolecular compounds, natural resins, waxes or and bituminous materials
    • C08L2666/14Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
    • C08L2666/22Macromolecular compounds not provided for in C08L2666/16 - C08L2666/20

Definitions

  • the present invention relates to a peelable seal layer formed from blends of polar and non-polar polyolefins, such peelable seal layers being useful for adhering adjacent thermoplastic films together to form a package.
  • Such packaging is easy to open by pulling the adjacent films apart due to the relative ease in rupturing the seal layer.
  • the present invention relates to a peelable seal layer formed from a thermoplastic polymer blend comprising (a) a non-polar, non-ionomeric polyolefin and (b) a polar ethylene copolymer having carbon monoxide functionality, and its use to adhere adjacent thermoplastic films together to form a package. Since the bonding strength of the thermoplastic films to one another and to the seal layer is greater than the internal cohesion strength of the peelable seal layer, the peelable seal layer provides for an easy to open package.
  • thermoplastic films sealed by vacuum skin packaging, thermoforming or other processes A wide variety of products, particularly perishable food products are sealed in packages using thermoplastic films sealed by vacuum skin packaging, thermoforming or other processes.
  • vacuum skin packaging a product is placed on a support of a film or of a tray of relatively rigid material and, by differential air pressure, a heated thermoplastic film above the product is molded down upon and around the product and against the support, the space between the upper film and the support having been evacuated.
  • the heated film forms a tight skin around the product and is sealed to the support.
  • the thermoplastic film is sealed to the flange-like edges of the support using heated sealing bars or similar equipment.
  • packaging processes for which the packaging material employs the peelable seal layer of the present invention include packaging in vertical or horizontal form-fill machines, as used in cereal packages and the like.
  • a problem that is encountered in these types of packaging is that the heated thermoplastic film seals so strongly to the support that it is difficult to separate them from each other in order to open the package.
  • An easy to open package of this type should be easily openable by manually pulling apart the two films, normally starting from a point like a corner of the package where the film has purposely not been sealed to the support. In this manner the use of scissors, a knife or other devices to open the package can be avoided.
  • a packaging material described in EP 0 192 131 Bl which addresses this problem consists of an upper and lower web of a thermoplastic material and a seal layer disposed there between and adhered to each of the opposite surfaces of the two webs, the adhesive seal strength of the seal layer to the first and second surfaces being greater than its internal cohesive strength.
  • the upper and lower webs are peeled apart manually, during which time the seal layer separates due to internal cohesive failure, whereby portions of the seal layer are left on the first and second surfaces.
  • the seal layer in these types of packaging materials can be a blend ofan ionomer and a modified ethylene- vinyl acetate copolymer. While these materials work well, they have the disadvantage that ionomers tend to be relatively costly in comparison to other thermoplastics, therefore commercially unattractive for certain end-uses.
  • thermoplastic polymer blend comprising (a) a non-polar polyolefin and (b) a polar ethylene copolymer having carbon monoxide functionality; whereby component (b) is present in the blend in a weight range between 1 and 90 %; and to provide a packaging material comprising the peelable seal layer and a thermoplastic film.
  • Non-polar, non-ionomeric thermoplastic polyolefin means any polyolefin polymer which is thermoplastic but which excludes polar ethylene copolymers and ionomers, as defined herein.
  • Useful polyolefins homopolymers include various polyethylenes, e.g. high density polyethylene (PE-HD), low density polyethylene (PE-LD), very low density polyethylene (PE-VLD), linear low density polyethylene (PE-LLD), as well as polypropylene.
  • Suitable polyolefin copolymers include copolymers of ethylene and a vinyl ester of an alkanoic acid (e.g. vinyl acetate) or an ester of an ethylenically unsaturated carboxylic acid (e.g. methyl acrylate, ethyl acrylate etc.).
  • Component (a) may also be a polypropylene (PP), which, as used herein, includes homopolymers of propylene as well as copolymers of polypropylene which can contain about 1 to about 20 weight percent ethylene or an alpha olefin comonomer of 4 to 16 carbon atoms.
  • the polypropylene can be highly crystalline isotactic or syndiotactic polypropylene.
  • the copolymer can be either a random or block copolymer.
  • the density of the PP or copolymer can be from about 0.88 to about 0.92 g cc; generally, from about 0.89 to about 0.91 g/cc.
  • PE-HD useful as a polyolefin resin of this invention has a density of about 0.941 to about 0.965 g/cc.
  • PE-HD is an established product of commerce and its manufacture and general properties are well known in the art.
  • PE-HD has a relatively broad molecular weight distribution, characterized by the ratio of weight average molecular weight to number average molecular weight of from about 20 to about 40.
  • PE-LD means both low and medium density polyethylene having densities of about 0.910 g/cc to about 0.940 g/cc.
  • the terns include linear polyethylene as well as copolymers of ethylene which are thermoplastic resins, but non-polar.
  • PE-VLD means polyethylene having a density below about 0.910 g/cc and includes linear polyethylene as well as copolymers of ethylene which are thermoplastic resins, but non-polar.
  • PE-LLD is a class of low density polyethylene characterized by little, if any long chain branching, in contrast to conventional PE-LD.
  • the processes for producing PE-LLD are well known in the art and commercial grades of this polyolefin are available.
  • the term PE-LLD means copolymers of ethylene and other alphaolefins such 1-octene, which tend to form clear films that are suitable for packaging applications.
  • Blends of the aforementioned homopolymers and copolymers may also be used in the invention.
  • Preferred component (a)'s according to the invention are PE-LD, PE-LLD and ethylene vinyl acetate (EVA).
  • thermoplastic polyolefins which are not included within the scope of the thermoplastic polyolefins defined for component (a), are well known thermoplastic materials, and may be described as copolymers containing ethylene and an olefinically unsaturated organic acid such as acrylic or methacrylic acid, wherein the acid is neutralized in whole or in part to produce a salt; c.f, for example US. Pat. Nos. 3,264,272, 3,404,134, 3,355,319 and 4,321,337.
  • Component (b) of the thermoplastic blend according to the invention is a polar ethylene copolymer having carbon monoxide functionality.
  • polar ethylene copolymers preferably consist essentially of ethylene, carbon monoxide and, optionally, one or more termonomers which are copolymerizable ethylenically unsaturated organic compounds.
  • Such termonomers are selected from the class consisting of unsaturated mono- and dicarboxylic acids of 3-20 carbon atoms, esters of such unsaturated mono-or dicarboxylic acids, vinyl esters of saturated carboxylic acids wherein the acid group has 1 - 18 carbon atoms, vinyl alkyl ethers wherein the alkyl group has 1-18 carbon atoms, acrylonitrile, methacrylonitrile, copolymerizable unsaturated hydrocarbons such as alpha-olefins of 3-12 carbon atoms, ring compounds such as norbomene and vinyl aromatic compounds.
  • these copolymers consist essentially of, by weight, (1) 30-80% ethylene (preferably 55-75%), (2) 2-30 % carbon monoxide (preferably 5-15%) and (3) 0-60% of one or more termonomers copolymerizable therewith to produce solid copolymers (preferably 20-50%).
  • More preferred copolymers include those in which the termonomer is vinyl acetate or an alkyl (1 -8 carbons) acrylate or alkyl methacrylate (particularly n-butyl acrylate).
  • Preferred component (b)'s according to the invention are ethylene-butylacrylate-carbon monoxide (EnBACO), ethylene-vinyl acetate-carbon monoxide (EVACO) and ethylene-carbon monoxide (ECO).
  • Component (b) will be present in the blend in a weight ratio between 1 and 90%, more preferably 3 to 20%.
  • thermoplastic films which are sealed together using the peelable seal film according to the present invention, may be the previously defined olefinic polymers of component (a), as well as polyesters, polyamides and other thermoplastic polymers.
  • Preferred thermoplastic webs will be made of low density polyethylene (PE-LD).
  • the resistance of the seal layer to peeling from the surface of the thermoplastic film is preferably about 1 - 12 N/15 mm, as measured according to ASTM D882.
  • the thermoplastic polymer blend according to the invention can be made by convention blending techniques. For example, they may be mixed in pellet form and then melt extruded.
  • the thickness of the seal layer is preferably in the range of about 5 to 60 ⁇ m, more preferably 6 to 20 ⁇ m.
  • the thickness of the thermoplastic film to which is adhered the seal layer is preferably in the range of about 10 to 100 ⁇ m, more preferably 20 to 50 ⁇ m.
  • the peelable seal layer may be applied to the thermoplastic film by conventional coextrusion processes to form packaging material.
  • Thermoplastic blends for peelable seal layers according to the present invention are prepared as followed.
  • Multilayer blown film with barrier Three different types of films can be produced: a. Monolayer blown film b. Multilayer blown film for lamination c. Multilayer blown film with barrier
  • Blends of thermoplastic resin pellets indicated in Table 1 are tumble blended and fed into a 30 mm laboratory Brabender Plasticoder extruder (PL 650) with a L/D ratio of 24 and equipped with a laboratory blown film unit Model
  • the processing temperature is set at about 210 °C. Peelable seal layers are extruded having a thickness of from 60-100 mm.
  • the extruded seal layers and the coextruded film for lamination produced on the standard, full scale blown film line are supported on oriented PET lidding film (12 ⁇ m in thickness).
  • the coextruded films with barrier are used directly in a way that the films are sealed against themselves in a fashion such that the peelable seal layer is positioned between the PET film at the indicated temperatures using a heat sealing machine (Kopp PK-110). Under fixed standard conditions (0.4 mPa pressure, 1 sec. dwell time) for each temperature (from 90 °C to 160 °C) the samples are produced.
  • the peel blend is coextruded with polyolefins like PE-LD and PE-HD.
  • the peel blend is produced by dry blending the thermoplastic resin pellet listed below in Tables 1 to 4.
  • the peel blend produced in the same way, is coextruded with PA6 (nylon 6) using a coextrudable adhesive (BYNEL* 3930 available from the DuPont Company).
  • EXAMPLE 90 100 110 120 130 140 150 160
  • EY* ELVALOY* (available from the DuPont Company)
  • the peelable seal layer ideally has a seal strength between 2 and 12 N/15 mm over a wide range of sealing temperatures. As indicated in Table 5 above, the control example demonstrates a steep and unacceptable increase in seal strength at sealing temperatures exceeding 100°C, whereas the examples according to the invention maintain good sealing level over the entire range of sealing temperatures typically encountered. In general (see Table 8), peelable seal layers containing higher levels of component (b) according to the invention will have
  • the peel value obtained is a function of the second phase concentration.
  • the type of ELVALOY* grade used has in general no dominating influence on the peel performance as the peel effect is related to polarity of the polymer generated by the CO-group (Ti ⁇ le 7 . A more significant effect is the

Abstract

The present invention relates to a peelable seal layer formed from blends of polar and non-polar polyolefins, such peelable seal layers being useful for adhering adjacent thermoplastic films together to form a package. Such packaging is easy to open by pulling the adjacent films apart due to the relative ease in rupturing the seal layer.

Description

TITLE PACKAGING SEAL LAYER
The present invention relates to a peelable seal layer formed from blends of polar and non-polar polyolefins, such peelable seal layers being useful for adhering adjacent thermoplastic films together to form a package. Such packaging is easy to open by pulling the adjacent films apart due to the relative ease in rupturing the seal layer.
More particularly, the present invention relates to a peelable seal layer formed from a thermoplastic polymer blend comprising (a) a non-polar, non-ionomeric polyolefin and (b) a polar ethylene copolymer having carbon monoxide functionality, and its use to adhere adjacent thermoplastic films together to form a package. Since the bonding strength of the thermoplastic films to one another and to the seal layer is greater than the internal cohesion strength of the peelable seal layer, the peelable seal layer provides for an easy to open package.
Background of the Invention
A wide variety of products, particularly perishable food products are sealed in packages using thermoplastic films sealed by vacuum skin packaging, thermoforming or other processes. In vacuum skin packaging, a product is placed on a support of a film or of a tray of relatively rigid material and, by differential air pressure, a heated thermoplastic film above the product is molded down upon and around the product and against the support, the space between the upper film and the support having been evacuated. The heated film forms a tight skin around the product and is sealed to the support. In the thermoforming process the thermoplastic film is sealed to the flange-like edges of the support using heated sealing bars or similar equipment.
Other packaging processes for which the packaging material employs the peelable seal layer of the present invention include packaging in vertical or horizontal form-fill machines, as used in cereal packages and the like. A problem that is encountered in these types of packaging is that the heated thermoplastic film seals so strongly to the support that it is difficult to separate them from each other in order to open the package. An easy to open package of this type should be easily openable by manually pulling apart the two films, normally starting from a point like a corner of the package where the film has purposely not been sealed to the support. In this manner the use of scissors, a knife or other devices to open the package can be avoided. A packaging material described in EP 0 192 131 Bl, which addresses this problem consists of an upper and lower web of a thermoplastic material and a seal layer disposed there between and adhered to each of the opposite surfaces of the two webs, the adhesive seal strength of the seal layer to the first and second surfaces being greater than its internal cohesive strength. To break the seal of such packages, the upper and lower webs are peeled apart manually, during which time the seal layer separates due to internal cohesive failure, whereby portions of the seal layer are left on the first and second surfaces. The seal layer in these types of packaging materials can be a blend ofan ionomer and a modified ethylene- vinyl acetate copolymer. While these materials work well, they have the disadvantage that ionomers tend to be relatively costly in comparison to other thermoplastics, therefore commercially unattractive for certain end-uses.
Accordingly, it is an object of the present invention to provide a lower cost alternative polymer blend for use as a peelable seal layer in packaging. More particularly, it is an object of the present invention to provide a peelable seal layer formed from a thermoplastic polymer blend comprising (a) a non-polar polyolefin and (b) a polar ethylene copolymer having carbon monoxide functionality; whereby component (b) is present in the blend in a weight range between 1 and 90 %; and to provide a packaging material comprising the peelable seal layer and a thermoplastic film.
Detailed Description of the Invention
Certain terms used herein have the following meanings. "Non-polar, non-ionomeric thermoplastic polyolefin" means any polyolefin polymer which is thermoplastic but which excludes polar ethylene copolymers and ionomers, as defined herein. Useful polyolefins homopolymers include various polyethylenes, e.g. high density polyethylene (PE-HD), low density polyethylene (PE-LD), very low density polyethylene (PE-VLD), linear low density polyethylene (PE-LLD), as well as polypropylene. Suitable polyolefin copolymers include copolymers of ethylene and a vinyl ester of an alkanoic acid (e.g. vinyl acetate) or an ester of an ethylenically unsaturated carboxylic acid (e.g. methyl acrylate, ethyl acrylate etc.).
Component (a) may also be a polypropylene (PP), which, as used herein, includes homopolymers of propylene as well as copolymers of polypropylene which can contain about 1 to about 20 weight percent ethylene or an alpha olefin comonomer of 4 to 16 carbon atoms. The polypropylene can be highly crystalline isotactic or syndiotactic polypropylene. The copolymer can be either a random or block copolymer. The density of the PP or copolymer can be from about 0.88 to about 0.92 g cc; generally, from about 0.89 to about 0.91 g/cc. PE-HD useful as a polyolefin resin of this invention, has a density of about 0.941 to about 0.965 g/cc. PE-HD is an established product of commerce and its manufacture and general properties are well known in the art. Typically, PE-HD has a relatively broad molecular weight distribution, characterized by the ratio of weight average molecular weight to number average molecular weight of from about 20 to about 40.
PE-LD, as used herein, means both low and medium density polyethylene having densities of about 0.910 g/cc to about 0.940 g/cc. The terns include linear polyethylene as well as copolymers of ethylene which are thermoplastic resins, but non-polar. PE-VLD, as used herein, means polyethylene having a density below about 0.910 g/cc and includes linear polyethylene as well as copolymers of ethylene which are thermoplastic resins, but non-polar.
PE-LLD is a class of low density polyethylene characterized by little, if any long chain branching, in contrast to conventional PE-LD. The processes for producing PE-LLD are well known in the art and commercial grades of this polyolefin are available. The term PE-LLD means copolymers of ethylene and other alphaolefins such 1-octene, which tend to form clear films that are suitable for packaging applications.
Blends of the aforementioned homopolymers and copolymers may also be used in the invention.
Preferred component (a)'s according to the invention are PE-LD, PE-LLD and ethylene vinyl acetate (EVA).
"Ionomers", which are not included within the scope of the thermoplastic polyolefins defined for component (a), are well known thermoplastic materials, and may be described as copolymers containing ethylene and an olefinically unsaturated organic acid such as acrylic or methacrylic acid, wherein the acid is neutralized in whole or in part to produce a salt; c.f, for example US. Pat. Nos. 3,264,272, 3,404,134, 3,355,319 and 4,321,337.
Component (b) of the thermoplastic blend according to the invention is a polar ethylene copolymer having carbon monoxide functionality. Useful such copolymers are described in US Patent 3,780,140. These polar ethylene copolymers preferably consist essentially of ethylene, carbon monoxide and, optionally, one or more termonomers which are copolymerizable ethylenically unsaturated organic compounds. Such termonomers are selected from the class consisting of unsaturated mono- and dicarboxylic acids of 3-20 carbon atoms, esters of such unsaturated mono-or dicarboxylic acids, vinyl esters of saturated carboxylic acids wherein the acid group has 1 - 18 carbon atoms, vinyl alkyl ethers wherein the alkyl group has 1-18 carbon atoms, acrylonitrile, methacrylonitrile, copolymerizable unsaturated hydrocarbons such as alpha-olefins of 3-12 carbon atoms, ring compounds such as norbomene and vinyl aromatic compounds.
In particular, these copolymers consist essentially of, by weight, (1) 30-80% ethylene (preferably 55-75%), (2) 2-30 % carbon monoxide (preferably 5-15%) and (3) 0-60% of one or more termonomers copolymerizable therewith to produce solid copolymers (preferably 20-50%). More preferred copolymers include those in which the termonomer is vinyl acetate or an alkyl (1 -8 carbons) acrylate or alkyl methacrylate (particularly n-butyl acrylate).
Preferred component (b)'s according to the invention are ethylene-butylacrylate-carbon monoxide (EnBACO), ethylene-vinyl acetate-carbon monoxide (EVACO) and ethylene-carbon monoxide (ECO). Component (b) will be present in the blend in a weight ratio between 1 and 90%, more preferably 3 to 20%.
The thermoplastic films, which are sealed together using the peelable seal film according to the present invention, may be the previously defined olefinic polymers of component (a), as well as polyesters, polyamides and other thermoplastic polymers. Preferred thermoplastic webs will be made of low density polyethylene (PE-LD).
The resistance of the seal layer to peeling from the surface of the thermoplastic film is preferably about 1 - 12 N/15 mm, as measured according to ASTM D882. The thermoplastic polymer blend according to the invention can be made by convention blending techniques. For example, they may be mixed in pellet form and then melt extruded.
The thickness of the seal layer is preferably in the range of about 5 to 60 μ m, more preferably 6 to 20 μ m. The thickness of the thermoplastic film to which is adhered the seal layer is preferably in the range of about 10 to 100 μ m, more preferably 20 to 50 μ m.
The peelable seal layer may be applied to the thermoplastic film by conventional coextrusion processes to form packaging material.
Examples
Thermoplastic blends for peelable seal layers according to the present invention are prepared as followed.
Preparation
Three different types of films can be produced: a. Monolayer blown film b. Multilayer blown film for lamination c. Multilayer blown film with barrier
The above films are produced in the following way: a. Monolayer blown film
Blends of thermoplastic resin pellets indicated in Table 1 are tumble blended and fed into a 30 mm laboratory Brabender Plasticoder extruder (PL 650) with a L/D ratio of 24 and equipped with a laboratory blown film unit Model
840805. The processing temperature is set at about 210 °C. Peelable seal layers are extruded having a thickness of from 60-100 mm.
The extruded seal layers and the coextruded film for lamination produced on the standard, full scale blown film line are supported on oriented PET lidding film (12 μm in thickness). The coextruded films with barrier are used directly in a way that the films are sealed against themselves in a fashion such that the peelable seal layer is positioned between the PET film at the indicated temperatures using a heat sealing machine (Kopp PK-110). Under fixed standard conditions (0.4 mPa pressure, 1 sec. dwell time) for each temperature (from 90 °C to 160 °C) the samples are produced.
b. Multilayer blown film without barrier
Using a standard production type of blown film line and extruders (extruders: 3 x 50 mm Reifenhauser, Smooth barrel / 3 zones heating/cooling plus 1 heating zone; screw: UO 26, with mixing head, length 4 D, feed zone length 8.8 D, compression ratio 3.5; die: three layers, Bermag, 200 mm, rotating, spiral design, die gap: 0.9 mm; airring: dual lip design, Western) the peel blend is coextruded with polyolefins like PE-LD and PE-HD. The peel blend is produced by dry blending the thermoplastic resin pellet listed below in Tables 1 to 4.
c. Multilayer blown film with barrier
Using the same three layer die described under b. the peel blend, produced in the same way, is coextruded with PA6 (nylon 6) using a coextrudable adhesive (BYNEL* 3930 available from the DuPont Company).
Table 1 Monolayer Peel Blends with High Loading Compositions
(parts by weight)
EXAMPLE
1 2 3 4 5 6 Control
EVA1 88 85 80 100
PE-LD2 80 85 80
EnBACO3 12 15 20 20 15
EnBACO4 20
Table 2 Influence of the matrix resin
Product 1 2 3 4
EVA1 88 85 - -
PE-LD2 - - 85 80
EnBACO3 12 15 15 20
Table 3 Influence of second phase material/modifier
Product 1 2 3 4
PE-LD2 15% 15% 15% 15%
EnBACO3 85%
EnVACO5 85%
EnBACO4 85%
EnBACO6 85% 05056
7
Table 4 Influence of second phase concentration
Product 1 2__ 3
PE-LD2 90 86 84 EnBACO4 10 14 16
1 Ethylene vinyl acetate (7.5% vinyl acetate; MI = 7)
2 Stamylan 2102 (available from DSM)
3 Ethylene butyl acrylate (30% n-butyl acrylate; 13% CO; MI = 12) 4 Ethylene butyl acrylate (30% n-butyl acrylate; 10% C; MI = 12)
5 Ethylene vinyl acetate (24 % Vinyl acetate; 10% CO; MI = 35)
6 Ethylene butyl acrylate (30% n-butyl acrylate; 10% CO; MI = 8) MI = melt index measured according to ASTM D 1238
Peel strength testing method
Sealed films so produced are peeled apart in a tensile testing machine (Zwick Model 1435) in machine direction using an angle of 90° according to ASTM D882. Typical crosshead speed used is 100 mm/min. The peel forces are read from a display and are plotted. The test is repeated for all five samples and the control, and the average value is calculated, as set forth in Tables 5 to 8.
Table 5 Monolayer Peel Strength (N/15 mm)
Temperatui re (°C)
EXAMPLE 90 100 110 120 130 140 150 160
1 0.5 4.3 6.0 6.2 6.5 6.5 6.5 6.5
2 - 3 .0 3 . 1 3.2 4.2 4.6 4.8 4.8
3 - 0.6 2. 1 2.2 2.3 2.5 2.7 2.9
4 - - 0.4 1.2 1.5 1.7 2.0 2.2
5 - 0.5 1.7 2.4 2.5 2.8 2.8 3.2
6 - 0.2 1.3 2.3 2.4 2.6 2.9 3.3 control 3.8 6.1 00 00 00 00 00 00
∞ Could not be peeled apart Table 6 Influence of Matrix Resin Peel Strength (N/15mm)
a: Matrix: = ELVAX* 3120 (available from the DuPont Company) Load 100°C 110°C 120°C 130°C 140°C 160°C
15 % 3.5 4.1 3.9 4.6 5 5.8 12 % 4.8 4.6 4.8 5.5 5.8 6.8
b: Matrix: = PE-LD2, MI=2
Load 100°C 110°C 120°C 130°C 140°C 160°C
20 % 0.1 4 4.6 4.6 4.2 4.8
15 % 0.1 5.6 5.6 8.2 8.1 8.2
Table 7 Influence of Second Phase Material/Modifier (15 % Load)
Second Phase 100°C 120°C 140°C 160°C
EY* 4051 2 3.4 4.5 5.5 EY* 741A 1.6 2.1 2.7 3.3 EY* 441 3.6 4.2 5.2 5.8 EY* 4015 3 4 5 6.1
Conditions:
15% EY* load in PE-LD2, MI=1
EY* = ELVALOY* (available from the DuPont Company)
Table 8 Influence of Second Phase Concentration - Peel Strength (N/15mm)
Influence of concentration (Second Phase - ELVALOY* HP 441)
Load 100°C 110°C 120°C 140°C 160°C
10 % 0 0.6 2.8 3.8 4.3 14 % 0 0.4 2.5 3.1 3.4 16 % 0 0.3 1.7 2.7 3
Conditions:
Blend of ELVALOY* HP 441 in PE-LD2 MI=1 Discussion of results
The peelable seal layer ideally has a seal strength between 2 and 12 N/15 mm over a wide range of sealing temperatures. As indicated in Table 5 above, the control example demonstrates a steep and unacceptable increase in seal strength at sealing temperatures exceeding 100°C, whereas the examples according to the invention maintain good sealing level over the entire range of sealing temperatures typically encountered. In general (see Table 8), peelable seal layers containing higher levels of component (b) according to the invention will have
10 lower seal strength .
The peel value obtained is a function of the second phase concentration. The type of ELVALOY* grade used has in general no dominating influence on the peel performance as the peel effect is related to polarity of the polymer generated by the CO-group (Tiφle 7 . A more significant effect is the
u_

Claims

/05056 PC17 1011
10
CLAIMS:
1. A seal layer for an easy to open package formed from a thermoplastic polymer blend comprising
(a) a non-polar, non-ionomeric polyolefin; and
(b) a polar ethylene copolymer having carbon monoxide functionality; whereby component (b) is present in the blend in a weight range between 1 and 90 %.
2. A seal layer according to claim 1 wherein component (a) comprises polyethylene or ethyl vinyl acetate.
3. A seal layer according to claim 1 wherein component (b) is present in a weight range between 2 and 30 %.
4. A seal layer according to claims 1 or 2 wherein component (b) comprises, by weight, (1) 30-80% ethylene, (2) 2-30 % carbon monoxide and (3) 0-60% of one or more termonomers copolymerizable therewith to produce solid copolymers.
5. A seal layer according to claim 4 wherein component (b) comprises, by weight, (1) 30-80% ethylene, (2) 5-15% carbon monoxide and (3) 20-50% n-butyl acrylate or vinyl acetate.
6. A seal layer according to claim 1 wherein component (b) comprises ethylene-butylacrylate-carbon monoxide, ethylene-vinyl acetate-carbon monoxide or ethylene-carbon monoxide.
7. Packaging material comprising a peelable seal layer according to claim 1 and a thermoplastic film.
8. Packaging material according to claim 7 wherein the thermoplastic film comprises polyethylene.
EP95930805A 1994-08-10 1995-08-09 Packaging seal layer Ceased EP0775051A4 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP95930805A EP0775051A4 (en) 1994-08-10 1995-08-09 Packaging seal layer

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP94202300 1994-08-10
EP94202300 1994-08-10
EP95930805A EP0775051A4 (en) 1994-08-10 1995-08-09 Packaging seal layer
PCT/US1995/010112 WO1996005056A1 (en) 1994-08-10 1995-08-09 Packaging seal layer

Publications (2)

Publication Number Publication Date
EP0775051A1 EP0775051A1 (en) 1997-05-28
EP0775051A4 true EP0775051A4 (en) 1997-11-19

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Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6133367A (en) * 1997-06-17 2000-10-17 E. I. Du Pont De Nemours And Company Ethylene vinyl acetate blends
US6361844B1 (en) 1999-01-27 2002-03-26 David T. Ou-Yang Release article and adhesive article comprising the release article
US6558809B1 (en) 1999-05-18 2003-05-06 The Dow Chemical Company Flexible, halogen-free, radio-frequency sealable films
US6465091B1 (en) 2000-03-27 2002-10-15 3M Innovative Properties Company Release article and adhesive article containing a polymeric release material
AT9750U1 (en) * 2006-07-13 2008-03-15 Teich Ag COMPOSITE MATERIAL, METHOD FOR THE PRODUCTION THEREOF AND ITS USE AS PACKAGING MATERIAL

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1378222A (en) * 1971-08-30 1974-12-27 Du Pont Ethylene interpolymer pellets of reduced tackiness and process of preparation
JPS60159853A (en) * 1984-01-31 1985-08-21 Rokuou Shoji Kk Light shielding masking film

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Publication number Priority date Publication date Assignee Title
GB1350290A (en) * 1971-05-18 1974-04-18 Ucb Sa Wrapping film capable of forming a peelable seal
US4247584A (en) * 1979-05-22 1981-01-27 American Can Company Composition comprising a blend of EVA polymers having differing VA contents; films and laminates made therefrom by extrusion; and heat-sealed food bags made from the laminates
DK262081A (en) * 1980-06-20 1981-12-21 Ucb Sa HEAT-SEALABLE PACKAGING MOVIES WHICH PROVIDE A SEPARATE SEAL
US4678713A (en) * 1984-08-31 1987-07-07 The Dow Chemical Company Co-extruded laminates containing carbon monoxide interpolymers
DE3504463A1 (en) * 1985-02-09 1986-08-14 W.R. Grace & Co., New York, N.Y. EASILY OPENABLE PACKING AND METHOD FOR THE PRODUCTION THEREOF
US5126176A (en) * 1990-02-27 1992-06-30 E. I. Du Pont De Nemours And Company Lidding for containers

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1378222A (en) * 1971-08-30 1974-12-27 Du Pont Ethylene interpolymer pellets of reduced tackiness and process of preparation
JPS60159853A (en) * 1984-01-31 1985-08-21 Rokuou Shoji Kk Light shielding masking film

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
PATENT ABSTRACTS OF JAPAN vol. 010, no. 003 (P - 418) 8 January 1986 (1986-01-08) *
See also references of WO9605056A1 *

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WO1996005056A1 (en) 1996-02-22
EP0775051A1 (en) 1997-05-28

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