AU671435B2 - Polymeric films - Google Patents

Polymeric films Download PDF

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Publication number
AU671435B2
AU671435B2 AU35541/93A AU3554193A AU671435B2 AU 671435 B2 AU671435 B2 AU 671435B2 AU 35541/93 A AU35541/93 A AU 35541/93A AU 3554193 A AU3554193 A AU 3554193A AU 671435 B2 AU671435 B2 AU 671435B2
Authority
AU
Australia
Prior art keywords
layer
voided
films
film according
propylene homopolymer
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
AU35541/93A
Other versions
AU3554193A (en
Inventor
David Williamson
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.)
Akzo Nobel Films Holding Ltd
Original Assignee
Courtaulds Films and Packaging Holdings Ltd
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
Priority claimed from GB929206603A external-priority patent/GB9206603D0/en
Application filed by Courtaulds Films and Packaging Holdings Ltd filed Critical Courtaulds Films and Packaging Holdings Ltd
Publication of AU3554193A publication Critical patent/AU3554193A/en
Application granted granted Critical
Publication of AU671435B2 publication Critical patent/AU671435B2/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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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
    • B32B27/16Layered products comprising a layer of synthetic resin specially treated, e.g. irradiated
    • 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
    • B32B27/18Layered products comprising a layer of synthetic resin characterised by the use of special additives
    • B32B27/20Layered products comprising a layer of synthetic resin characterised by the use of special additives using fillers, pigments, thixotroping agents
    • 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
    • B32B3/00Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar form; Layered products having particular features of form
    • B32B3/26Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar form; Layered products having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer
    • 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
    • B32B2250/242All polymers belonging to those covered by group B32B27/32
    • 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
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/30Properties of the layers or laminate having particular thermal properties
    • B32B2307/31Heat sealable
    • 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
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/50Properties of the layers or laminate having particular mechanical properties
    • B32B2307/514Oriented
    • B32B2307/518Oriented bi-axially
    • 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
    • B32B2323/046LDPE, i.e. low density polyethylene

Description

r iv
AUSTRALIA
PATENTS ACT 1990 COMPLETE SPECIFICATION NAME OF APPLICANT(S): Courtaulds Films (Holdings) Limited ADDRESS FOR SERVICE: DAVIES COLLISON CAVE Patent Attorneys 1 Little Collins Street, Melbourne, 3000.
C.,'r tti t r t I INVENTION TITLE: Polymeric films The following statement is a full description of this invention, including the best method of performing it known to me/us:- C t I t 4 P:\OPER\MLA\35541-93.191 9/7/96 This invention concerns polymeric films and especially polypropylene films having puncture resistance combined with good gloss.
It has been proposed hitherto in Research Disclosure 226030A to impart puncture resistance to polymeric films by the inclusion of a layer consisting of a blend of polypropylene with a low density polyethylene. Although such layers impart some degree of puncture resistance, depending upon their relative thickness compared with that of the film itself, they have the disadvantage of reducing the gloss of the films.
According to the present invention there is provided a biaxially oriented polymeric film comprising a first layer of a propylene homopolymer contain a pigmentary amount of titanium dioxide, a second layer on one side of the first layer said second layer being of a non-voided propylene homopolymer, a third layer on the other surface of the core layer, the third layer being of a voided propylene homopolymer containing a voiding agent and a pigmentary 15 amount of titanium dioxide, and an outer heat sealable layer on the said third layer.
Films of the present invention have shown good puncture resistance combined with particularly good gloss when viewed from the side having the non-voided polypropylene layer next to the heat seal layer. In addition, films of the present invention can provide tamper evidence after sealing the other side of the films to a substrate, for example by the voided i layer rupturing when such seals are peeled and thereby giving evidence of tampering with the seal.
The said first layer of propylene homopolymer generally serves as a core layer, i.e. it is 25 usually the thickest layer of the films.
The said first layer can be voided or non-voided, voiding for example being used to reduce the overall density of the films. However, voiding of this layer can affect the gloss of the heat seal layer thereon and it is therefore generally preferred that the degree of viding of this 30 layer be kept low whilst providing the films with reduced density through voiding. The first 1- 1-1 1 NS P:\OPER\MLA35541-93.191 -9/7/96 -2layer can contain up to 10 percent, e.g. about 5 per cent, by weight of voiding agent but lower amounts, e.g. up to 2 percent or more preferably about 1 percent, by weight are usually required if the gloss of the heat seal layer on the said second layer is not to be significantly adversely affected.
Voiding of the said third layer, and where desired the first, layers can be effected using organic or inorganic voiding agents, for example polyamides, e.g. nylons, polyesters, e.g.
polyethylene terephthalate or polyisobutylene.
t I 0e I ei I i
I
S C I I i *11
ZL
terephthalate, or chalk. The use of voiding agents with polypropylene is well known in the art, as are the particle sizes of the voiding agent required to effect voiding.
Voiding of the third layer is preferably effected using from to 15 percent by weight of voiding agent based on the weight of the third layer, it being preferred to use larger amounts than are necessary merely to induce voiding when it is requi-ed to impart the ability to show evidence of tampering of seals between the film and a substrate to which the film has been heat sealed. Tamper evidence can usually "i be provided by the third layer containing up to 25 percent by weight of voiding agent, especially chalk, and although percent by weight or less of voiding agent can be used for the purpose it is generally preferred to use at least 20 percent by weight of voiding agent, all such percentages being based on the weight of the third layer. Large amounts of voiding agent can, however, be undesirable as they can lead to excessive weakening of the films.
Any or all of the said first, second and third polypropylene layers can include a pigment. Such pigments are additional to any voiding agents which may be included in such layers to impart properties to the film resulting from voiding, the second layer being non-voided. Examples of pigments which S"can be used include titanium dioxide. The particle size of the pigment will usually be sub-micronic in order to avoid voiding of the layer in which it is present.
Although a pigment can be present in all three of the said first, second and third layers, it is generally preferred that at least the third of said layers should contain a pigment, but usually in an amount of not more than percent by weight of the third layer. It is also preferred that the first of said layers should contain a pigment, and it is preferred to use not more than 20 percent by L C I 4 weight of the first layer. Although it is generally not preferred to include a pigment in the said second layer since such pigments often reduce the gloss of the heat seal layer on the said second layer, it is often necessary to do so to impart the desired degree of opacity to the films.
The second layer can, therefore, contain up to 14 percent by weight of a non-voiding pigment based on the weight of the second layer, although lesser amounts are generally preferred.
The said second layer has a heat sealable layer coextensive therewith, for example formed from a copolymer containing units derived from propylene and at least one of ethylene and but-l-ene, or a linear low density polyethylene, e.g.
propylene/ethylene or propylene/but-l-ene copolymers, or :propylene/ethylene/but-l-ene terpolymers.
Films in accordance with the present invention will usually include one or more layers coextensive with the said third layer to provide the films with sealability. For example, the films can include a heat sealable layer, itself preferably coextensive with the said third layer, or they can include at least one coextensive layer, for example of a non-heat sealable polymer, to which can be applied a hot or cold sealable layer, for example a cold seal adhesive composition or polyvinylidene chloride. Examples of heat sealable layers which can be used include copolymers of propylene with at least one of ethylene and but-l-ene, i.e.
propylene/ethylene and propylene/but-l-ene copolymers, and propylene/ethylene/but-l-ene terpolymers, or linear low density polyethylene. When sealable compositions are to be applied to the said third layer, they will usually be applied to a layer of polypropylene homopolymer coextensive with the said third layer.
The said third layer can furthermore be provided with one or more layers which impart other properties to the films. For example, a metallizable layer on the said third layer can form an outer surface of the films.
Films in accordance with the present invention can include one or more additives used in the art, for example to provide antiblock, antistatic or slip properties to the films.
Films in accordance with the present invention can be produced by known methods, and advantageously by coextrusion of the respective layers followed by biaxial stretching which is preferably effected sequentially.
Films in accordance with the present invention can be a prepared of a variety of thicknesses, the individual layers also being of a variety of thicknesses. For example, the films can be from 30 to 60nm thick, e.g. about 40m thick.
The said first layer is preferably the thickest layer, for example from 20 to 401um thick, with the third layer usually being the second thickest layer, for example from 5 to 15m i S *thick. The second layer can be up to 10im or more, but it "is usually sufficient for the second layer to be about 54m thick in order to impart high gloss to the heat seal layer thereon.
The heat seal layer or layers will usually be not more than 2jum thick, for example about lpm thick, in order to confer heat sealability. However, thicker heat seal layers can be used when it is desired to impart a particularly high degree of heat sealability.
The following Examples are given by way of illustration only. All parts are by weight unless stated otherwise.
6 6 Example 1 A five-layer polymer web was produced by coextruding through a slot die a core layer of propylene homopolymer containing 2 percent by weight of titanium dioxide of mean particle size 0.8pm with a layer of propylene homopolymer on one side and a layer of propylene homopolymer containing 5 percent by weight of titanium dioxide of mean particle size 0.8um and about 20 percent by weight of chalk having a mean particle size of about 3.5um, and outer layers of a propylene/ethylene (4 percent ethylene) copolymer on either side of the polypropylene homopolymer layers.
The fiv.e-layer web was then stretched 4.5 times in the Sdirection of extrusion over heated rollers at 110 0 C with H different peripheral speeds, and 10 times in the transverse direction in a stenter oven at 156°C. The resulting five layer, biaxially oriented film was then subjected to corona discharge on the surface formed by the copolymer on the non-voided homopolymer layer, and the film was wound up.
The film had a total thickness of 40pm, the central, core layer containing titanium dioxide being non-voided and 23pum thick, with the voided layer containing the chalk being thick, and the non-voided, non-pigmented homopolymer layer being 5im thick. The two copolymer layers were each lmw thick.
SThe resulting film showed a gloss of 52 for the copolymer surface on the non-voided homopolymer compared with 5 for the opposite film surface. The film had an optical density of 0.52 and a density of 0.70g/cm 3 Its puncture resistance was 0.52 using the 1mm probe and 3.19 using the 3mm probe.
Example 2 A five-layer polymer web was produced by coextruding through 7 a slot die a core layer of propylene homopolymer containing percent by weight of titanium dioxide of mean particle size 0.84m and 5 percent by weight of calcium carbonate of mean particle size 31um with a layer of propylene homopolymer containing 10 percent by weight of titanium dioxide of mean particle size 0.8pm on one side and a layer of propylene homopolymer containing 5 percent by weight of titanium dioxide of mean particle size 0.8u4m and 14 percent by weight of chalk having a mean particle size of about 3un, an outer layer of a propylene/ethylene (4 percent ethylene) copolymer on the polypropylene homopolymer layer not containing chalk, and an outer layer of a propylene/ethylene/butene terpolymer on the other side.
The five-layer web was then stretched 4.5 times in the direction of extrusion over heated rollers at 110 0 C with different peripheral speeds, and 10 times in the transverse direction in a stenter oven at 156 0 C. The resulting five layer, biaxially oriented film was then subjected to corona discharge treatment on the surface formed by the propylene/ethylene copolymer layer, and the film was wound up. The film had a total thickness of 44pm, the central, core layer containing titanium dioxide being voided and 28.5im thick, with the voided layer containing 14 percent of chalk being Sun thick, and the non-voided, pigmented hompolymer layer being 8im thick. The propylene/ethylene copolymer layer was lium thick and the propylene/ethylene/butene terpolymer layer was 1.5im thick.
The resulting film showed a gloss of 30 for the copolymer surface on the non-voided hompolymer compared with 5 for the opposite film surface. *The film had an optical density of 0.71 and a density of 0.69/cm 3 Its puncture resistance was 0.52 using 1mm probe and 3.11 using the 3mm probe.
8 Example 3 A five-layer film was produced as described in Example 2 except that the core layer contained 7 percent by weight of calcium carbonate of mean particle size lim instead of percent by weight of mean particle size 3um.
The resulting film showed a gloss of 39 for the copolymer surface on the non-voided homopolymer compared with 5 for the opposite film surface. The film had an optical density of 0.75 and a density of 0.69/cm 3 Its puncture resistance was 0.49 using the 1mm probe and 2.97 using the 3mm probe.
S Example 4 (Comparison) A three-layer polymer web was produced by coextruding through a slot die a core layer of propylene homopolymer containing 5 percent by weight of calcium carbonate of 3mun mean particle size and 2 percent by weight of titanium dioxide having a mean particle size of 0.8mun with an outer layer on each side of the core layer and consisting of a S: propylene/ethylene (4 percent ethylene) copolymer.
The web was then biaxially stretched to produce a three-layer film with an overall thickness of 43pm, the core layer being 40m thick and the two outer layers each being 1.51m thick.
Both outer surfaces of this film had a gloss of 10, the film having an optical density of 0.56 and a density of 0.69g/cm 3 Its puncture resistance was 0.43 using the 1mm probe and 1.75 using the 3mm probe.
The films of Examples 1, 2 and 3 showed a considerably higher gloss for one of their surfaces than that of either of the surfaces of the comparison film of Example 4.
Lr I I- P:\OPER\ILA\35541-93. 191 -9/796 -9- Furthermore, when the films of Examples 1, 2 and 3 were heat sealed to a polyethlyene container to form a heat seal on the container, they gave evidence of tampering when peeled from the container as a result of the voided layer rupturing when peeling is effected. They also showed evidence of tampering when peeled apart after heat sealing to themselves.
Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stater integer or group of integers but not the exclusion of any other integer or group of integers.
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rr r rr rri r

Claims (9)

1. A biaxially oriented polymeric film comprising a first layer of a propylene homopolymer containing a pigmentary amount of titanium dioxide, a second layer on one side of the first layer said second layer being of a non-voided propylene homopolymer, a third layer on the other surface of the first layer, the third layer being of a voided propylene homopolymer containing a voiding agent and a pigmentary amount of titanium dioxide, and an outer heat sealable layer on the said third layer.
2. A film according to claim 1, wherein the first layer is non-voided.
3. A film according to claim 1, wherein the first layer is voided.
4. A film according to claim 3, wherein the first layer contains chalk as the voiding agent.
A film according to any of the preceding claims, wherein the second layer contains a pigmentary amount of titanium dioxide.
6. A film according to any of the preceding claims, wherein the third layer contains chalk Sas the voiding agent. S
7. A film according to any of the preceding claims, wherein and a heat sealable layer on the said third layer, the said third layer contains from 14 to 25 percent by weight of chalk as S 25 the voiding agent.
8. A film according to any of the preceding claims, having an outer layer on the said second layer. 4 P:\OPERMA35541-93.191 10/1196
9. A film according to claim 1, substantially as herein described with reference to any of Examples 1 to 3. DATED this 10th day of July, 1996. COURTAULDS FILMS (HOLDINGS) LTD. By its Patent Attorneys DAVIES COLLISON CAVE 440 S Y -L ABSTRACT 99 r Biaxially oriented polymeric films consisting of a first layer of a propylene homopolymer having on one side thereof and coextensive therewith a second layer of a non-voided propylene homopolymer and on the other side thereof and coextensive therewith a third layer of a voided propylene homopolymer, the said second layer having a heat sealable layer thereon and coextensive therewith. Films of the invention have puncture resistance combined with good gloss.
AU35541/93A 1992-03-26 1993-03-26 Polymeric films Ceased AU671435B2 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GB929206603A GB9206603D0 (en) 1992-03-26 1992-03-26 Polymeric films
GB9206603 1992-03-26
GB9304470 1993-03-05
GB9304470A GB2265332B (en) 1992-03-26 1993-03-05 Polymeric films

Publications (2)

Publication Number Publication Date
AU3554193A AU3554193A (en) 1993-11-11
AU671435B2 true AU671435B2 (en) 1996-08-29

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Family Applications (1)

Application Number Title Priority Date Filing Date
AU35541/93A Ceased AU671435B2 (en) 1992-03-26 1993-03-26 Polymeric films

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EP (1) EP0562867A1 (en)
AU (1) AU671435B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4443411A1 (en) * 1994-12-07 1996-06-13 Hoechst Ag Sealable, white-opaque, biaxially oriented polypropylene multilayer film, process for its preparation and its use
GB9706901D0 (en) * 1997-04-04 1997-05-21 Rexam Med Packaging Ltd Polymeric films
DE69820240T2 (en) * 1997-04-04 2004-10-14 Amcor Flexibles Winterbourne Ltd. PLASTIC FILMS AND PACKAGES MADE THEREOF

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0312226A1 (en) * 1987-10-05 1989-04-19 COURTAULDS FILMS & PACKAGING (HOLDINGS) LTD. Polymeric films
AU2983392A (en) * 1991-12-03 1993-06-10 Trespaphan Gmbh Polymeric films

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3940173A1 (en) * 1989-12-05 1991-06-06 Hoechst Ag DOUBLE-SIDED SEALABLE, BIAXIAL-ORIENTED POLYOLEFIN MULTILAYER FILM, THEIR PRODUCTION AND THEIR USE
US4965123A (en) * 1989-12-29 1990-10-23 Mobil Oil Corporation Opaque oriented polymeric film structure and method of preparing same
US5091236A (en) * 1991-05-14 1992-02-25 Mobil Oil Corporation Multi-layer high opacity film structures

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0312226A1 (en) * 1987-10-05 1989-04-19 COURTAULDS FILMS & PACKAGING (HOLDINGS) LTD. Polymeric films
AU2983392A (en) * 1991-12-03 1993-06-10 Trespaphan Gmbh Polymeric films

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Publication number Publication date
AU3554193A (en) 1993-11-11
EP0562867A1 (en) 1993-09-29

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