PVDC formulation and heat shrinkable film

Information

  • Patent Grant
  • 9365687
  • Patent Number
    9,365,687
  • Date Filed
    Wednesday, December 31, 2008
    16 years ago
  • Date Issued
    Tuesday, June 14, 2016
    8 years ago
Abstract
The present invention is directed to a polymer blend formulation and to heat shrinkable film, bags, pouches and the like made therefrom. The invention is further directed to a method of producing a heat shrinkable film with the proper gas permeability properties so that it is ideal for packaging and preservation of gassing cheese.
Description
RELATED APPLICATIONS

This application claims the benefit of European Application No. 08150005.0, filed Jan. 2, 2008, the entire disclosure of which is herein incorporated by reference.


TECHNICAL FIELD

The present invention is directed to a polymer blend formulation and to heat shrinkable film, bags, pouches and the like made therefrom. The invention is further directed to a method of producing a heat shrinkable film with the proper gas permeability properties so that it is ideal for packaging and preservation of gassing cheese.


BACKGROUND

Gassing cheese products are generally characterized by the emission of carbon dioxide during their curing process. Packaging films used for packaging of such cheese must be able to allow carbon dioxide escape, so that a possible “ballooning” effect is avoided. At the same time, oxygen permeability should be as low as possible, so that the oxidation-deterioration of the cheese is minimized.


Heat shrinkable films are often used for gassing cheese packaging due to the good aesthetic appearance that heat shrinkability induces. High transparency of the pack is also important, so that possible consumers are attracted by the pack.


The majority of heat shrinkable films used in this area comprise PVDC as barrier layer. PVDC is difficult to extrude and quite easy to burn and deteriorate during the extrusion process.


PVDC formulations like for example described in prior art patents are commonly used.


Generally these PVDC formulations incorporate high percentage of plasticizers or stabilizers in order to increase the permeability to CO2. Common plasticizers/stabilizers are epoxidized compounds like epoxidized soybean oil, epoxidized linseed oil, etc. One negative effect is that these compounds tend to migrate from the PVDC layer to other layers, thus creating delaminations and, most dangerously, change of barrier properties as time passes. This is an undesirable phenomenon.


So, several features that should characterize a heat shrinkable film intended for use in packaging of gassing cheese are


1. High shrinkage


2. Excellent optics


3. Efficient heat sealability so that bags can be made


4. Avoidance of plasticizer use


5. Good processability of PVDC, no oxidation during extrusion


6. High CO2 permeability, not changing over time


7. High O2 barrier, not changing over time.


These features are matched with the PVDC combination of the present invention and with the heat shrinkable films we further advice.


SUMMARY OF THE INVENTION

It is therefore the object of this invention to make a polymer blend providing the above characteristics.


This is solved by a polymer blend comprising

    • A. PVDC polymer
    • B. Ethylene vinyl acetate with more than 40% vinyl acetate (per weight)
    • C. PVC
    • D. Epoxidized oil compound and optionally other additives.


For example, the invention comprises a PVDC combination with the following recipe:


Blend of

    • a copolymer PVDC as base resin
    • epoxidized materials less than 2% per weight
    • ethylene vinyl acetate copolymer with percentage of 40 to 50% vinyl acetate per weight
    • PVC content more than 0% and less than 2%
    • silica and talc
    • possibly other materials like silicon polymers, high density polyethylene, tetrasodium pyrophospthate


It is further the object of this invention to extrude the above described PVDC formulation without deterioration even in high shear rates.


It is further the object of this invention to produce a multilayer film incorporating a PVDC layer comprising the above described recipe. The other layers may preferably comprise ethylene alpha olefin copolymers, propylene alpha olefin copolymers, propylene ethylene copolymers, styrene polymers or ionomers.


THE DEFINITIONS USED IN THE FOLLOWING ARE AS FOLLOWS

The term “film” refers to a flat or tubular flexible structure of thermoplastic material.


The term “heat shrinkable” refers to a film that shrinks at least 10% in at least one of the longitudinal and transverse directions when heated at 90° C. for 4 seconds. The shrinkability is measured according to ASTM 2732 with water as a heating medium. This test method covers the determination of the degree of unrestrained linear thermal shrinkage at given specimen temperatures of a plastic film and sheeting of 0.76 mm thickness or less.


All measurement methods mentioned herein are readily available for the skilled person. For example, they can be obtained from the American National Standards Institute at: www.webstore.ansi.org


The phrase “longitudinal direction” or “machine direction” herein abbreviated “MD” refers to a direction along the length of the film.


The phrase “outside layer” refers to the film layer which comes in immediate contact with the outside environment (atmosphere).


The phrase “middle layer” refers to the layer which is exactly in the middle between outer and sealing layer, such as outer layer/next layer/middle layer/next layer/sealing layer.


The phrase “inner layer” refers to the film layer that comes in direct contact with the product packed. This is also called “sealing layer” as this layer must be hermetically sealed in order to protect the product from ingress of air.


As used herein, the term “homopolymer” refers to a polymer resulting from polymerization of a single monomer.


As used herein, the term “copolymer” refers to a polymer resulting from polymerization of at least two different polymers.


As used herein, the term “polymer” includes both above types.


As used herein the term “polyethylene” identifies polymers consisting essentially of the ethylene repeating unit. The ones that have a density more than 0.940 are called high density polyethylene (HDPE), the ones that are have less than 0.940 are low density polyethylene (LDPE).


As used herein the phrase “ethylene alpha olefin copolymer” refers to polymers like linear low density polyethylene (LLDPE), medium density polyethylene (MDPE), very low density polyethylene (VLDPE), ultra low density polyethylene (ULDPE), metallocene catalysed polymers and polyethylene plastomers and elastomers.


As used herein the phrase “styrene polymers” refers to styrene homopolymer such as polystyrene and to styrene copolymers such as styrene-butadiene copolymers, styrene-butadiene-styrene copolymers, styrene-isoprene-styrene copolymers, styrene-ethylene-butadiene-styrene copolymers, ethylene-styrene copolymers and the like.


As used herein the phrase “ethylene methacrylate copolymers” refers to copolymers of ethylene and methacrylate monomer. The monomer content is preferably less than 40%.


As used herein the phrase “ethylene vinyl acetate copolymer” refer to copolymers of ethylene and vinyl acetate.


As used herein, the term EVOH refers to saponified products of ethylene vinyl ester copolymers. The ethylene content is typically in the range of 25 to 50%.


As used herein the term PVDC refers to a vinylidene chloride copolymer wherein a major amount of the copolymer comprises vinylidene chloride and a minor amount of the copolymer comprises one or more monomers such as vinyl chloride and/or alkyl acrylates and methacrylates.


As used herein the term polyamide refers to homopolymers and copolymers. Typical examples are polyamide 6, polyamide 66, polyamide 6/66, polyamide 6/12 and MXD nylon.


As used herein the term “polypropylene” refers to any homopolymer, copolymer, terpolymer, tetrapolymer etc. that includes mer units of propylene. The term as used in the present application includes homopolymers, random copolymers, propylene alpha olefin copolymers, propylene ethylene copolymers propylene-ethylene-alpha olefin copolymers and other propylene polymers.


As used herein, the term “polybutylene” refers to homopolymer of butene-1 or to copolymers with ethylene or propylene.







DETAILED DESCRIPTION

The PVDC used in this invention is preferably a copolymer of vinylidene chloride and vinyl chloride or a copolymer of vinylide chloride and methyl acrylate or a blend of both.


The percentage of EVA used preferably is less than 20% per weight of the total blend.


The percentage of PVC used preferably is less than 2% per weight of the total polymer blend.


The percentage of the epoxidized oil compound preferably is less than 5% per weight of the total polymer blend.


The plasticizer-stabilizer used is preferably one of epoxidized soybean oil, epoxidized linseed oil.


The blend of EVA copolymer, PVC and additives can be a ready made compound in pallet or powder form. A preferred compound is BAYMOD L2450 purchased by the company Lanxess.


The epoxidized soybean oil or epoxidized linseed oil may be preblended to the PVDC copolymer or blended at the same time with the rest of components. Well known mixing techniques may be used to secure that the final blend is homogeneous.


Powder is preferable when the PVDC used is also powder.


In a second aspect, a plastic film is disclosed comprising a layer comprising the composition as mentioned above.


Preferably, the film is comprising five layers, where the middle layer comprises the composition as defined above and the film is heat shrinkable.


In the outside layer the following materials may be used:

    • 1. A polypropylene homopolymer or copolymer having a vicat softening point of less than 105° C. measured under ASTM D 1525. Preferably the polymer is homogeneous, having low molecular weight distribution and comonomer distribution.
    • 2. PP polymer such as random copolymer or homopolymer (among others)
    • 3. Polyethylene polymer such as an alpha olefin copolymer with density 0.860 to about 0.960 or such as an ethylene ester copolymer
    • 4. a cyclic olefin copolymer
    • 5. a styrene polymer
    • 6. an ionomer or a methacrylic acid copolymer
    • 7. a polyamide (care is needed in the barrier property evaluation).


A preferred version comprises a:

    • 1. styrene butadiene copolymer
    • 2. a blend of styrene butadiene copolymer and an ethylene alpha olefin copolymer


Between the inner heat sealing layer and the oxygen barrier layer may exist further layers that could comprise any of the polymers mentioned in the possibilities for inner heat sealing layer. Preferred materials are ethylene vinyl acetate, ethylene alpha olefin copolymers, EMA polymers, polypropylene copolymers, polybutylene, styrene homopolymers or copolymers.


Between the outer layer and the PVDC layer, one or more layers may be present.


Preferred materials are ethylene vinyl acetate, ethylene alpha olefin copolymers, EMA polymers, polypropylene copolymers, polybutylene, styrene homopolymers or copolymers.


Typical materials used in the sealing layer are ethylene alpha olefin copolymers and polypropylene copolymers.


Any of the layers described above may also include additives well known in the art such as slip agents, antiblock, polymer processing aids, antistatic, antifog, acid scavengers, odor scavengers and the like. A person skilled in the art may select the right additives according to any particular needs.


In a preferred version of the application, the film is irradiated with e beam radiation of levels from 1 to 10 MRAD.


The material of this invention is preferably biaxially oriented and heat shrinkable.


In a further aspect, the invention comprises a bag or pouch made by the film of the invention and a cheese packed in such a film.


EXAMPLES
Example 1

A 5 layer film is produced in a double bubble commercial line with the following structure:


Inner (sealing) layer, 100% PL1, thickness 25 microns


Adjacent layer 93% E1+7% ADDITIVES, thickness 5 microns


Barrier layer PVDC 1, thickness 4.5 microns


Adjacent layer 30% M1+65% E3+5% ADDITIVES, thickness 11 microns


Outer layer 100% SB1, thickness 7.5 microns


See table 1, 2


Example 2

Inner (sealing) layer, 100% PL1


Adjacent layer 93% E1+7% ADDITIVES


Barrier layer PVDC 2


Adjacent layer 30% M1+65% E2+5% ADDITIVES


Outer layer 100% SB1


Thicknesses the same as example 1.


Comparative Example 3

A 5 layer film is produced in a double bubble (the double bubble method is described in U.S. Pat. No. 3,456,044) commercial line with the following recipe


Inner (sealing layer), 100% PL1


Adjacent layer 93% E1+7% ADDITIVES


Barrier layer PVDC commercial grade


Adjacent layer 30% M1+65% E2+5% ADDITIVES


Outer layer 95% S1+5% ADDITIVES


The difference between the examples 1 and 2 which represent the invention and ex. 3 is that the PVDC formulation used in ex. 3 is believed to have a much bigger percentage of migratory materials like epoxidized oils (more than 5% in the blend). These materials are used in order to adjust the permeability to CO2 and O2.


The present invention proposes another way to adjust the permeability, without sacrificing the processability of the blend. As seen in table 3, the formulations of the invention are much more stable even after 3 months.


With the inventive formulations, problems like delaminations of PVDC are also much improved.


All the samples were e-beam radiated with a dose of 4 MRAD prior to bag making.














TABLE 1








Melt







Index
Density
Melting point


Type
Description
Manufacturer
g/10 min
g/cm3
° C.




















E1
EVA
Dupont 3135 X
0.35
0.93
95


E2
EVA
Dupont 3165
0.7
0.94
89


S1
SB
DK13
10
1.01



COPOLYMER


M1
EMA copolymer
ARKEMA LOTRYL
2-3.5
0.95
61




29MAO3


P1
Ethylene
DOW AFFINITY PL
1
0.902
100



octene
1880



copolymer









Manufacture of the Three PVDC

PVDC 1. Blend of PVDC copolymer (which already incorporates about 2% per weight epoxidized soybean oil) with 11% BAYMOD L2450.


PVDC 2. Blend of PVDC copolymer (which already incorporates about 2% per weight epoxidized soybean oil) with 16% BAYMOD L2450. This blend is used for packaging of special “high gassing” types of cheeses.


PVDC 3. Commercial PVDC with more than 5% epoxidized soybean oil.


Measurements were done three days after the irradiation step.













TABLE 3







O2
CO2
CO2 transmission



transmission
transmission
After 3 months





















Example 1
155
810
750



Example 2
410
2100
1950



Example 3
140
780
450










O2 transmission is measured in 23C, 75% RH according to ASTM D3985. Units are cc/m2*atm*day.


CO2 transmission is measured according to internal method using a MOCON type instrument. Units are cc/m2*atm*day. Conditions 23° C. at 0% RH.


We see that the combinations 1 and 2 are much more stable overtime. This is beneficial as it reduces the risks of pack “ballooning” after a certain period of time.

Claims
  • 1. A film comprising five layers, where a middle layer comprises a polymer blend comprising: a) a polyvinylidene chloride (PVDC) polymer, wherein the PVDC polymer is a copolymer wherein a major amount of the copolymer comprises vinylidene chloride and a minor amount of the copolymer comprises one or more monomers selected from the group consisting of vinyl chloride, alkyl acrylate and alkyl methacrylate;b) unmodified ethylene vinyl acetate (EVA) with more than 40% vinyl acetate (per weight);c) polyvinyl chloride (PVC); andd) an epoxidized oil compound and optionally other additives.
  • 2. A film according to claim 1, where the film is heat shrinkable.
  • 3. The film according to claim 1, wherein an outer layer of the film comprises one of: a polypropylene polymeran ethylene alpha olefin copolymera styrene butadiene polymera polyamidea polybutene and/oran ethylene vinyl alcohol (EVOH) polymer.
  • 4. The film of according to claim 1, wherein a sealing layer of the film comprises ethylene alpha olefin copolymer.
  • 5. The film according to claim 1, wherein the film is irradiated.
  • 6. The film according to claim 1, having a flat or tubular form.
  • 7. A bag or pouch made from the film of claim 1.
  • 8. A cheese packed in a film according to claim 1.
  • 9. A film comprising at least an outer layer, a sealing layer, and a layer comprising a polyvinylidene chloride (PVDC) blend, wherein the outer layer is a layer which comes into immediate contact with the outside environment and the sealing layer is a layer that comes into direct contact with a product when the film is used to pack a product, and wherein the layer comprising the PVDC blend comprises: a) a PVDC polymer, wherein the PVDC polymer is a copolymer wherein a major amount of the copolymer comprises vinylidene chloride and a minor amount of the copolymer comprises one or more monomers selected from the group consisting of vinyl chloride, alkyl acrylate and alkyl methacrylate;b) unmodified ethylene vinyl acetate (EVA) with more than 40% vinyl acetate (per weight);c) polyvinyl chloride (PVC); andd) an epoxidized oil compound and optionally other additives.
  • 10. The film according to claim 9, wherein the film is heat shrinkable.
  • 11. The film according to claim 9, wherein the outer layer of the film comprises one of: a polypropylene polymeran ethylene alpha olefin copolymera styrene butadiene polymera polyamidea polybutene and/oran ethylene vinyl alcohol (EVOH) polymer.
  • 12. The film according to claim 9, wherein the sealing layer of the film comprises ethylene alpha olefin copolymer.
  • 13. The film according to claim 9, wherein the film is irradiated.
  • 14. The film according to claim 9, having a flat or tubular form.
  • 15. The film according to claim 9, wherein the percentage of EVA in the PVDC blend is less than 20% per weight of the total PVDC blend.
  • 16. The film according to claim 9, wherein the percentage of PVC in the PVDC blend is less than 2% per weight of the total PVDC blend.
  • 17. The film according to claim 9, wherein the percentage of epoxidized oil compound in the PVDC blend is less than 5% per weight of the total PVDC blend.
  • 18. A bag or pouch made from the film of claim 9.
  • 19. A cheese packed in a film according to claim 9.
  • 20. A film comprising at least an outer layer, a sealing layer, and a barrier layer, wherein the outer layer is a layer which comes into immediate contact with the outside environment and the sealing layer is a layer that comes into direct contact with a product when the film is used to pack a product, and wherein the barrier layer comprises a polymer blend comprising: a) a polyvinylidene chloride (PVDC) polymer, wherein the PVDC polymer is a copolymer wherein a major amount of the copolymer comprises vinylidene chloride and a minor amount of the copolymer comprises one or more monomers selected from the group consisting of vinyl chloride, alkyl acrylate and alkyl methacrylate;b) unmodified ethylene vinyl acetate (EVA) with more than 40% vinyl acetate (per weight);c) polyvinyl chloride (PVC); andd) an epoxidized oil compound and optionally other additives.
Priority Claims (1)
Number Date Country Kind
08150005 Jan 2008 EP regional
US Referenced Citations (144)
Number Name Date Kind
2380054 Lautmann Aug 1943 A
2376185 Randall May 1945 A
3299194 Golike Jan 1967 A
3356192 Cameron Dec 1967 A
3456044 Pahlke Jul 1969 A
3536192 Couper Oct 1970 A
3846569 Kaplan Nov 1974 A
3908336 Forslund Sep 1975 A
3956229 Bollen et al. May 1976 A
4064296 Bornstein et al. Dec 1977 A
4207364 Nyberg Jun 1980 A
4254869 Heier Mar 1981 A
4362834 Lefevre et al. Dec 1982 A
4399181 Yoshimura et al. Aug 1983 A
4595433 Ford et al. Jun 1986 A
4612221 Biel et al. Sep 1986 A
4650721 Ashcraft et al. Mar 1987 A
4705707 Winter Nov 1987 A
4716061 Winter Dec 1987 A
4786561 Fong Nov 1988 A
4801486 Quacquarella et al. Jan 1989 A
4863769 Lustig et al. Sep 1989 A
4869049 Richards et al. Sep 1989 A
4911979 Nishimoto et al. Mar 1990 A
4912149 Robeson et al. Mar 1990 A
4934529 Richards et al. Jun 1990 A
4941310 Kristen Jul 1990 A
4976898 Lustig et al. Dec 1990 A
4977022 Mueller Dec 1990 A
4990562 Chou et al. Feb 1991 A
5001192 Sun Mar 1991 A
5034281 Kawasaki et al. Jul 1991 A
5079051 Garland et al. Jan 1992 A
5169708 Amaral et al. Dec 1992 A
5179168 Hirasawa Jan 1993 A
5256351 Lustig et al. Oct 1993 A
5256428 Lustig et al. Oct 1993 A
5296580 Matsunaga et al. Mar 1994 A
5298202 Schirmer Mar 1994 A
5302402 Dudenhoeffer et al. Apr 1994 A
5397613 Georgelos Mar 1995 A
5562958 Walton et al. Oct 1996 A
5593747 Georgelos Jan 1997 A
5645788 Bekele Jul 1997 A
5698279 Vicik Dec 1997 A
5834077 Babrowicz Nov 1998 A
5837335 Babrowicz Nov 1998 A
5851610 Ristey et al. Dec 1998 A
5888615 Mascarenhas et al. Mar 1999 A
5983607 Mihalov et al. Nov 1999 A
6013378 White et al. Jan 2000 A
6058998 Kristen May 2000 A
6065272 Lecomte May 2000 A
6074715 Lind et al. Jun 2000 A
6088996 Maruyama Jul 2000 A
6146726 Yoshii et al. Nov 2000 A
6221410 Ramesh et al. Apr 2001 B1
6258423 Giori Jul 2001 B1
6274246 Eggers et al. Aug 2001 B1
6299984 Forloni Oct 2001 B1
6346285 Ramesh Feb 2002 B1
6406763 Wolf et al. Jun 2002 B1
6458437 Ito et al. Oct 2002 B1
6506463 Cahill et al. Jan 2003 B1
6514583 Ahlgren et al. Feb 2003 B1
6516588 Jensen et al. Feb 2003 B2
6531198 Lind et al. Mar 2003 B2
6534137 Vadhar Mar 2003 B1
6558760 Paleari et al. May 2003 B1
6572959 Buongiorno et al. Jun 2003 B1
6592975 Ueyama et al. Jul 2003 B1
6663905 Ennis et al. Dec 2003 B1
6682792 Schmal et al. Jan 2004 B2
6777046 Tatarka et al. Aug 2004 B1
6960635 Stevens et al. Nov 2005 B2
6984695 Brown et al. Jan 2006 B2
7473473 Verrocchi Jan 2009 B2
7611770 Kennedy et al. Nov 2009 B2
7736726 McAllister et al. Jun 2010 B2
8129006 Ginossatis Mar 2012 B2
8697211 Gkinosatis Apr 2014 B2
20020038535 Jensen et al. Apr 2002 A1
20020119334 Shepard et al. Aug 2002 A1
20020172834 Rivett et al. Nov 2002 A1
20030008084 Vicik et al. Jan 2003 A1
20030012900 Wolf et al. Jan 2003 A1
20030073785 Okada et al. Apr 2003 A1
20030124452 Nair et al. Jul 2003 A1
20030213804 Chomik et al. Nov 2003 A1
20030218022 Chomik et al. Nov 2003 A1
20030220453 Ebara et al. Nov 2003 A1
20040020175 Stravitz Feb 2004 A1
20040043238 Wuest et al. Mar 2004 A1
20040048086 Kennedy et al. Mar 2004 A1
20040065052 Ramesh et al. Apr 2004 A1
20040074904 Share et al. Apr 2004 A1
20040157077 Roussos Aug 2004 A1
20040194433 Chomik et al. Oct 2004 A1
20050044819 Chomik et al. Mar 2005 A1
20050064123 Chomik et al. Mar 2005 A1
20050129811 Kraimer et al. Jun 2005 A1
20050147778 Tai et al. Jul 2005 A1
20050191439 Hirose et al. Sep 2005 A1
20050235611 Roussos Oct 2005 A1
20050239961 Saraf et al. Oct 2005 A1
20050271877 Ginossatis Dec 2005 A1
20060010837 Jurus Jan 2006 A1
20060172143 Breese et al. Aug 2006 A1
20060177616 Barber et al. Aug 2006 A1
20060177641 Breese et al. Aug 2006 A1
20060199030 Liang et al. Sep 2006 A1
20060199912 Fuchs et al. Sep 2006 A1
20060254219 Alipour et al. Nov 2006 A1
20060272767 Kreitman et al. Dec 2006 A1
20060283153 Nakano Dec 2006 A1
20060286323 Siegel et al. Dec 2006 A1
20070042089 Grah Feb 2007 A1
20070082150 Ginossatis Apr 2007 A1
20070089688 Nitzsche et al. Apr 2007 A1
20070178285 Rasanen et al. Aug 2007 A1
20080003332 Ginossatis Jan 2008 A1
20080070047 Rehkugler et al. Mar 2008 A1
20080095960 Schell et al. Apr 2008 A1
20080115463 Wilson May 2008 A1
20080255311 Chang et al. Oct 2008 A1
20080274314 Gkinosatis Nov 2008 A1
20080274328 Gkinosatis Nov 2008 A1
20080305220 Gkinosatis Dec 2008 A1
20090013656 Nasiatka et al. Jan 2009 A1
20090176117 Gkinosatis Jul 2009 A1
20090191392 Gkinosatis Jul 2009 A1
20090240227 Toro et al. Sep 2009 A1
20090263599 Gkinosatis Oct 2009 A1
20100028574 Gkinosatis Feb 2010 A1
20100032098 Lalli et al. Feb 2010 A1
20100034939 Gkinosatis Feb 2010 A1
20110159263 Gkinosatis Jun 2011 A1
20120279181 Gkinosatis Nov 2012 A1
20120289645 Tice et al. Nov 2012 A1
20130019568 Gkinosatis Jan 2013 A1
20130209797 Gkinosatis Aug 2013 A1
20130227916 Gkinosatis Sep 2013 A1
20150010764 Gkinosatis Jan 2015 A1
20150210454 Gkinosatis Jul 2015 A1
Foreign Referenced Citations (59)
Number Date Country
511 195 Jul 1980 AU
0 005 660 Nov 1979 EP
0 286 407 Oct 1988 EP
0 402 043 Dec 1990 EP
0 472 418 Feb 1992 EP
0 627 466 Dec 1994 EP
627465 Dec 1994 EP
0 810 087 Dec 1997 EP
1 072 632 Jan 2001 EP
0 930 349 Jun 2003 EP
1 060 077 Jun 2003 EP
1 131 205 Dec 2004 EP
1 514 680 Mar 2005 EP
1 415 930 Apr 2006 EP
1 770 116 Apr 2007 EP
1 854 625 Nov 2007 EP
08162162.5 Aug 2008 EP
1 985 440 Oct 2008 EP
1 985 443 Oct 2008 EP
1 995 058 Nov 2008 EP
2 077 239 Jul 2009 EP
2 077 297 Jul 2009 EP
2 085 216 Aug 2009 EP
2 111 979 Oct 2009 EP
2 147 783 Jan 2010 EP
792290 Mar 1958 GB
1 140 765 Jan 1969 GB
2 236 531 Apr 1991 GB
2236531 Apr 1991 GB
62107810 May 1987 JP
03 200534 Sep 1991 JP
07196818 Aug 1995 JP
07206004 Aug 1995 JP
07206005 Aug 1995 JP
07206006 Aug 1995 JP
2002-234975 Aug 2002 JP
2003-159761 Jun 2003 JP
2005-047959 Feb 2005 JP
2005-335111 Dec 2005 JP
2006-247870 Sep 2006 JP
567768 Nov 2009 NZ
567767 May 2010 NZ
WO9601736 Jan 1996 WO
WO9746384 Dec 1997 WO
WO9821274 May 1998 WO
WO9821276 May 1998 WO
WO9944824 Sep 1999 WO
WO9957612 Nov 1999 WO
WO0061439 Oct 2000 WO
WO0123268 Apr 2001 WO
WO0226493 Apr 2002 WO
WO03020515 Mar 2003 WO
WO 2006053885 May 2006 WO
WO2006075141 Jul 2006 WO
WO2006102152 Sep 2006 WO
WO2007053603 May 2007 WO
WO2008091321 Jul 2008 WO
WO2008118554 Oct 2008 WO
WO 2011029597 Mar 2011 WO
Non-Patent Literature Citations (106)
Entry
European Search Report corresponding to European Patent Application No. 08173056.6-2109 dated Mar. 16, 2009.
ASTM BS2782.
ASTM D1003.
ASTM D1525.
ASTM D2732.
Annonymous, “Advantages of metallocene ethylene olymer resins in multilayer stretch films,” Research Disclosure, Mason Publications, Hampshire, GB. vol. 419, No. 26 (1999).
Annonymous, “Some benefits from the use of metallocene ethylene polymers in blown and cast films,” Research Disclosure, Mason Publications, Hampshire, GB. vol. 392, No. 54 (1996).
ASTM D3418-08. Standard Test Method for Transition Temperatures and Enthalpies of Fusion and Crystallization of Polymers by Differential Scanning Calorimetry. American National Standards Institute. Dec. 2008. www.astm.org.
ASTM D882-09. Standard Test Method for Tensile Properties of Thin Plastic Sheeting. American National Standards Institute. Jan. 2009. www.astm.org.
ASTM F1927-07. Standard Test Method for Determination of Oxygen Gas Transmission Rate, Permeability and Permeance at Controlled Relative Humidity Through Barrier Materials Using a Coulometric Detector. American National Standards Institute. Aug. 2007. www.astm.org.
English abstract of JP 2005-103902, USUI, Apr. 2005.
European Search Report corresponding to European Patent Application No. 08173057.4-2307 dated Sep. 22, 2009.
Extended European Search Report corresponding to European Patent Application No. 05021541.7-2115 dated Dec. 2, 2005.
Extended European Search Report corresponding to European Patent Application No. 08156814 dated Oct. 9, 2008.
Extended European Search report corresponding to European Patent Application No. 09151289.7-2124 dated Jun. 8, 2009.
Interview Summary corresponding to U.S. Appl. No. 12/150,261 dated Dec. 28, 2010.
Machine Translation of JP 2005-103902, USUI, Apr. 2005.
Official Action corresponding to U.S. Appl. No. 11/528,741 dated Mar. 30, 2010.
Official Action corresponding to U.S. Appl. No. 11/528,741 dated Jan. 4, 2011.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Sep. 15, 2009.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Feb. 5, 2010.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Jul. 15, 2010.
Official Action corresponding to U.S. Appl. No. 12/150,168 dated Feb. 16, 2011.
Official Action corresponding to U.S. Appl. No. 12/150,261 dated Oct. 27, 2009.
Official Action corresponding to U.S. Appl. No. 12/150,261 dated Jul. 7, 2010.
Official Action corresponding to U.S. Appl. No. 12/319,149 dated Oct. 15, 2009.
Official Action corresponding to U.S. Appl. No. 12/319,149 dated Jul. 7, 2010.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated Sep. 14, 2010.
Official Action corresponding to U.S. Appl. No. 12/508,233 dated Mar. 9, 2011.
ASTM D3985. Standard Test Method for Oxygen Gas Transmission Rate Through Plastic Film and Sheeting Using a Coulometric Sensor. American National Standards Institute. pp. 1-7. www.astm.org.
Official Action corresponding to U.S. Appl. No. 12/150,261 dated Mar. 22, 2011.
Official Action corresponding to U.S. Appl. No. 12/154,662 dated Mar. 29, 2011.
Official Action corresponding to U.S. Appl. No. 12/319,149 dated Mar. 22, 2011.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated Mar. 16, 2011.
“15.13×EA—Ethylene Vinyl Acetate (EVA) Copolymers (>50% Ethylene)—European Adhesives,” The ChemQuest Group, Inc. http://web.archive.org/web/20080219220919/http://www.chemquest.com/store/ethylene-vinyl-acetate-copolymers-european-adhesives.html (Aug. 26, 2011) (2 pages).
“DuPont™ Elvax® 3170,” DuPont Packaging & Industrial Polymers. 3 pages (2004) http://web.archive.org/web/20060516114601/http://www2.dupont.com/Elvax/en—US/assets/downloads/vax3170.pdf.
Extended European Search Report corresponding to European Patent Application No. 08154742.4-2124 dated Jul. 2, 2009.
Harper, “Modern Plastics Handbook,” McGraw-Hill: New York, New York. pp. 3.17-3.22 (2000).
Hough, M., and Dolbey, R., “Modern Plastics Compendium, vol. 1—Key Properties and Sources,” Smithers Rapra Technology. pp. 87-124 (1995).
Huskić, M., and {hacek over (S)}ebenik, A., “Characterization of Crosslinked Ethylene-Vinylacetate Copolymers,” Polymer International. vol. 31, No. 1 pp. 41-44 (1993).
Interview Summary corresponding to U.S. Appl. No. 12/150,261 dated Sep. 21, 2011.
Interview Summary corresponding to U.S. Appl. No. 12/322,347 dated Sep. 21, 2011.
Kipp, “Plastic Material Data Sheets,” MatWeb (2004) (5 pages).
Official Action corresponding to U.S. Appl. No. 11/528,741 dated May 18, 2011.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Jun. 20, 2011.
Official Action corresponding to U.S. Appl. No. 12/154,662 dated Aug. 18, 2011.
Official Action corresponding to U.S. Appl. No. 12/512,361 dated Aug. 31, 2011.
Petrie, “Handbook of Adhesives and Sealants,” 2nd Edition. McGraw-Hill: New York, New York. pp. 465-466 (2007).
“Polymer Blend,” IUPAC Compendium of Chemical Terminology. 2nd Edition (1997).
Interview Summary corresponding to U.S. Appl. No. 12/319,149 dated Oct. 17, 2011.
Notice of Allowance corresponding to U.S. Appl. No. 11/528,741 dated Oct. 28, 2011.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Jan. 30, 2012.
Official Action corresponding to U.S. Appl. No. 12/150,168 dated Sep. 23, 2011.
Official Action corresponding to U.S. Appl. No. 12/154,662 dated Jan. 18, 2012.
Official Action corresponding to U.S. Appl. No. 12/319,149 dated Dec. 2, 2011.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated Oct. 26, 2011.
Official Action corresponding to U.S. Appl. No. 12/508,233 dated Nov. 23, 2011.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Jan. 17, 2012.
Unisource—Moisture Barrier & Oxygen Barrier Transmission Rates; <http://www.unisourcelink.com/packaging/pdf/MoistureBarrier.pdf> (Retrieved on Jan. 10, 2012).
“Filling and sealing of containers” in Fellows, P.J. (2000). Food Processing Technology—Principles and Practice (2nd Edition). Woodhead Publishing.
Extended European Search Report corresponding to European Patent Application No. 10193414.9—1217 dated May 9, 2011.
Interview Summary corresponding to U.S. Appl. No. 11/801,609 dated Jul. 31, 2012.
Interview Summary corresponding to U.S. Appl. No. 12/150,261 dated Jun. 12, 2012.
Interview Summary corresponding to U.S. Appl. No. 12/319,149 dated Jun. 15, 2012.
Interview Summary corresponding to U.S. Appl. No. 12/508,233 dated Apr. 26, 2012.
Interview Summary corresponding to U.S. Appl. No. 13/722,323 dated Jan. 22, 2016.
Notice of Allowance corresponding to U.S. Appl. No. 12/150,168 dated Nov. 25, 2013.
Notice of Allowance corresponding to U.S. Appl. No. 13/157,876 dated Nov. 12, 2015.
Official action corresponding to European Patent Application No. 10 193 414.9—1303 dated Oct. 29, 2014.
Official Action corresponding to New Zealand Patent Application No. 626181 dated Jun. 18, 2014.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Feb. 2, 2016.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Jun. 12, 2015.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Nov. 29, 2013.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Sep. 24, 2014.
Official Action corresponding to U.S. Appl. No. 12/150,168 dated Apr. 26, 2013.
Official Action corresponding to U.S. Appl. No. 12/150,168 dated Aug. 14, 2012.
Official Action corresponding to U.S. Appl. No. 12/150,261 dated Jan. 31, 2012.
Official Action corresponding to U.S. Appl. No. 12/319,149 dated Aug. 27, 2012.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated Aug. 1, 2014.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated May 15, 2012.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated May 20, 2015.
Official Action corresponding to U.S. Appl. No. 12/426,496 dated Feb. 7, 2012.
Official Action corresponding to U.S. Appl. No. 12/508,233 dated Jun. 6, 2012.
Official Action corresponding to U.S. Appl. No. 12/512,361 dated May 2, 2012.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Apr. 24, 2014.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Jan. 7, 2015.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Jul. 24, 2013.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Sep. 16, 2015.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Sep. 25, 2012.
Official Action corresponding to U.S. Appl. No. 13/157,876 dated Jun. 2, 2014.
Official Action corresponding to U.S. Appl. No. 13/157,876 dated Mar. 3, 2015.
Official Action corresponding to U.S. Appl. No. 13/157,876 dated Nov. 19, 2013.
Official Action corresponding to U.S. Appl. No. 13/523,462 dated Jan. 30, 2015.
Official Action corresponding to U.S. Appl. No. 13/523,462 dated Sep. 21, 2015.
Official Action corresponding to U.S. Appl. No. 13/682,160 dated Jan. 29, 2016.
Official Action corresponding to U.S. Appl. No. 13/682,160 dated Jun. 15, 2015.
Official Action corresponding to U.S. Appl. No. 13/722,323 dated Jan. 7, 2015.
Official Action corresponding to U.S. Appl. No. 13/722,323 dated Jul. 17, 2015.
Official Action corresponding to U.S. Appl. No. 13/722,323 dated Mar. 27, 2014.
Official Action corresponding to U.S. Appl. No. 14/612,175 dated Dec. 9, 2015.
Official Action corresponding to United Kingdom Patent Application No. GB1020302.4 dated Dec. 11, 2014.
Official Action corresponding to United Kingdom Patent Application No. GB1020302.4 dated Jul. 2, 2014.
“Baymod L 2450,” Product Data Sheet, LANXESS. (2 pages) (2007).
“Elvaloy resins,” Product Data Sheet, DuPont Packaging & Industrial Polymers. (2 pages) (2010).
“Polybutylene terephthalate (PBT),” 1 page <http://www.britannica.com/EBchecked/topic/468341/polybutylene-terephthalate-PBT> (Accessed on Jun. 13, 2012).
“Polybutylene terephthalate,” Britannica Online Encyclopedia. pp. 1-3 (Accessed on Sep. 7, 2011) <http://www.britannica.com/EBchecked/topic/468341/polybutylene-terephthalate-PBT>.
Related Publications (1)
Number Date Country
20090196962 A1 Aug 2009 US