Thin film for waste packing cassettes

Information

  • Patent Grant
  • 9604430
  • Patent Number
    9,604,430
  • Date Filed
    Thursday, December 20, 2012
    12 years ago
  • Date Issued
    Tuesday, March 28, 2017
    7 years ago
Abstract
The present invention refers to a polymeric film comprising an odor barrier material and being able to pack malodorous waste.
Description

The present U.S. patent application claims priority to European Patent Application No. 12 154 500.8, filed Feb. 8, 2012, the disclosure of which is incorporated herein by reference in its entirety.


The present invention refers to a polymeric film comprising an odor barrier material and being able to pack malodorous waste.


A lot of waste products produce smells that are annoying to the environment. Examples are decayed food, kid nappies and cat litter.


In the prior art there are many films that could be used for protection from malodors. As well known in the art, the use of materials like EVOH, PVDC, polyacrylonitrile is recommended in order to not allow malodors escape from the container (e.g. bag or other configuration) and create an unpleasant atmosphere.


There are also a lot of known configurations of packing a certain length of film (e.g. 20 meters) in a compressed form (e.g. in a cassette). Examples of the representative cassettes are shown in U.S. Pat. No. 4,934,529 or U.S. Pat. No. 3,356,192.


Generally the cassette comprises a tubular core, casing wall and cassette bottom. The film is pulled through the area between the lid of the cassette and the casing wall. The flexible tubing is dispensed from the cassette. After the malodorous item (e.g. diaper) is thrown into the bag the core is rotated and the flexible tube is twisted so that it closes as hermetically as possible the waste/environment area.


To dispose the next diaper the user pushes the next portion of film. The previous hermetically closed diaper is pushed downwards and the new diaper is packed in a new configuration. All these different packs are stored in a bin which is periodically emptied. Separation of one pack to the other can be done by various means. A rotary knife is preferred.


Recently other methods of packing waste have been emerged such as the use of adhesive films. In prior art patent application US2008/0115463 use of adhesive film is suggested as an alterative way to pack malodorous items. However, there is no detail about how the film could be formulated or any hint about its structure.


The challenge the present application tackles is to achieve the following film characteristics:

    • 1. Low thickness material for economical production and competitiveness.
    • 2. Odor barrier.
    • 3. Possibility to bond to itself by a slight hand pressure
    • 4. Easy unwinding of the reel.
    • 5. Good mechanical properties to handle consumer abuse during using.


      Film Characteristics


We have surprisingly found that all these features can be achieved with a very lightweight multilayer film with a grammage of less than 25 g/m2. This is extremely beneficial for the environment as multilayer films are extremely difficult to be produced with so small weight per surface. Prior art films are characterized by a weight per surface ratio of more than 25 g/m2 and often of more than 30 g/m2.


SUMMARY OF THE INVENTION

The invention is directed to a multilayer film with a weight per surface ratio of less than 25 g/m2 used in malodorous item packaging, where the film comprises at least one oxygen barrier material and a layer comprising a self-adhesive material.


The films according to the invention show superior results regarding tensile strength and elongation characteristics. Furthermore, the films according to the invention were comparable in odor testing compared to commercially available films.


DEFINITIONS

In this application the following definitions are used:


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 (MD) and transverse (TD) directions when heated at 90° C. for 4 seconds. The shrinkability is measured in water according to ASTM 2732. For temperatures like 100° C. or more, glycerine is used as a reference liquid.


The term “total heat shrinkability” refers to the sum of heat shrinkability at the MD (machine) direction and heat shrinkability at the TD (transverse) direction. In all cases, ASTM 2732 is used for measurement of shrinkabilities.


The term “multilayer” refers to a film comprising 2 or more layers.


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


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


The phrase “outer 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 “polyolefin” refers to any polymerized olefin, which can be linear, branched, cyclic, aliphatic, substituted or unsubstituted. More specifically, included in the term polyolefin are homopolymers of olefin, copolymers of olefin, copolymers of an olefin and a non olefinic comonomer (such as ester) etc.


Specific examples include polyethylene homopolymer, polypropylene homopolymer, polybutene homopolymer, ethylene alpha olefin copolymer, propylene alpha olefin copolymer, butene alpha olefin copolymer, ionomer, ethylene ester copolymer etc.


As used herein the term “polyethylene” identifies polymers consisting essentially of the ethylene repeating unit, i.e. more than 50% of it are formed by ethylene repeating units. 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 catalyzed polymers and polyethylene plastomers and elastomers.


As used herein the term “homogenous ethylene alpha olefin copolymers” refer to ethylene alpha olefin copolymers having a molecular weight distribution less than 2.7 as measured by GPC (gas permeation chromatography). Typical examples of these polymers are AFFINITY® from Dow or EXACT® from Exxon.


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” or EMA refers to copolymers of ethylene and methacrylate monomer. The monomer content is less than 40% per mol.


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


As used herein the phrase “ethylene ester copolymer” includes any polymer made from ethylene and ester monomers. It is obvious that this term includes EVAs, EMAs and other polymers.


As used herein the term “oxygen barrier polymer” refers to polymers which have the property to limit the passage of oxygen through a film or a layer comprising the polymer. Common materials are EVOH, PVDC or polyamide.


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% per mol. All the later references to EVOH ethylene content will be in % per mol.


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. A major amount is defined as one of more than 50%.


As used herein the term “polyamide” refers to homopolymers and copolymers. Polyamide 6, polyamide 66, polyamide 12, polyamide 6/66, polyamide 6/12, polyamide elastomers, MXD polyamides and other copolymers are specifically useful for the invention.


As used herein the term “polyester” refers to polymers comprising terephthalate units. Examples of polyesters are PET (polyethylene terephthalate), PBT (polybutylene terephthalate), polyester elastomer (block copolymer comprising ester or ether units), PTT (polytrimethylene terephthalate) and other similar polymers.


As used herein, the term “ionomer” comprises the copolymers of ethylene and methacrylic or acrylic acid being metal neutralized. An example of such material is Surlyn from Dupont.


As used herein, the term “polypropylene” refers to polymers incorporating propylene structural units. Examples of these, are homo polypropylenes, random copolymers of propylene and ethylene, block copolymers of propylene and ethylene, copolymers or blends of propylene and rubber (such as blends of polypropylene and ethylene propylene rubber), propylene ethylene alpha olefin terpolymers and others.


The above polymers may be isotactic, syndiotactic or atactic. Isotactic configuration is preferred.


As used herein the term “self-adhesive material” refers to materials that when produced into film form can be bonded to themselves by pressure only without the need to be heated. The bonding level which separates self-adhesive from non self-adhesive materials is 5 g/15 mm when the bonding has been done on a 100×1500 mm film piece with a pressure of 3 bar under ambient conditions and with a contact time of 5 seconds. Values of equal to or more than 5 g/15 mm according to this test show that the material is self-adhesive whereas values of lower than 5 g/15 mm show the film being non self-adhesive.


As used herein the term “substantially non resilient material” refers to materials or material compounds comprising at least 40% per weight inorganics like calcium carbonate, titanium dioxide, wollastonite, mica, glass fibers, dolomite and the like. The rest percentage per weight can be polyethylene, polypropylene, styrene polymer or other thermoplastic material.


As used herein the term “tackifier” refers to low molecular weight materials used to increase the stickiness of the surface of an adhesive. Typical examples are rosins and their derivatives, terpenes and modified terpenes, hydrogenated hydrocarbon resins, C5 aliphatic resins, C9 aromatic resins, C5/C9 resins, terpene/phenol resins and the like.


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.


All percentages are based on weight per weight ratio, except when otherwise stated.







DETAILED DESCRIPTION OF THE INVENTION

According to a first aspect the present invention is directed to a multilayer film with weight per surface ratio of less than 25 g/m2 used in malodorous item packaging, where the film comprises a layer comprising a self-adhesive material and a layer comprising an oxygen barrier material.


According to a further aspect the present invention is directed to a multilayer film with weight per surface ratio of less than 20 g/m2 used in malodorous item packaging, where the film comprises a layer comprising self-adhesive material and a layer comprising an oxygen barrier material.


According to a further aspect the present invention is directed to a multilayer film with weight per surface ratio of less than 15 g/m2 used in malodorous item packaging, where the film comprises a layer comprising self-adhesive material and a layer comprising an oxygen barrier material.


In a further preferred embodiment, the film comprises the construction:


OUTER LAYER/ABUSE LAYER/INTERMEDIATE LAYER/BARRIER LAYER/INTERMEDIATE LAYER/ABUSE LAYER/INNER LAYER


In another preferred embodiment, the film comprises the construction:


OUTER LAYER/INTERMEDIATE LAYER/BARRIER LAYER/INTERMEDIATE LAYER/INNER LAYER


Detailed description of layers:


Barrier Layer


In a preferred embodiment of the invention, the oxygen barrier material is EVOH. The EVOH used preferably has an ethylene content less than 48%, more preferably less than 44%, more preferably less than 38%, more preferably from 27 to 32% ethylene per mol.


In another preferred embodiment, the oxygen barrier material comprises polyamide.


The oxygen barrier material preferably has a weight of less than 3 g/m2, more preferably less than 2 g/m2 and even more preferably less than 1.5 g/m2.


Outer Layer


In a preferred embodiment, the outer layer comprises self-adhesive material.


In a further preferred embodiment, the weight per surface ratio of the outer layer is less than 6 g/m2, more preferably less than 5 g/m2.


In a preferred version, the self-adhesive material comprises ethylene vinyl acetate copolymer where the vinyl acetate weight ratio is at least 20%, more preferably at least 25% even more preferably at least 25%, even more preferably at least 40%.


In another preferred version the self-adhesive material is a propylene ethylene copolymer where the ethylene content is at least 10% per weight.


In another preferred version the self-adhesive material comprises an ethylene alpha olefin copolymer with density less than 0.9 g/cm3, even more preferably less than 0.880 g/m3. Preferred alpha olefins are butene, hexene or octene.


In another preferred version, the self-adhesive material comprises a maleic anhydrite grafted polyolefin. Examples are maleic anhydrite grafted ethylene vinyl acetate copolymer of linear low density polyethylene.


In another preferred version, the self-adhesive material comprises styrene copolymers with a styrene content of less than 50% per weight. Typical examples are styrene butadiene styrene copolymers, styrene isoprene styrene copolymers, styrene ethylene butadiene copolymers and the like.


In another preferred version, the self-adhesive material comprises ethylene methyl acrylate copolymer with a methyl acrylate content of at least 20% per weight.


In another preferred version, the self-adhesive material comprises ethylene butyl acrylate material with a butyl acrylate content of at least 15% per weight.


In another preferred version, the self-adhesive material comprises poly-isobutylene polymer (PIB) or polybutene copolymer.


In a further preferred version, the self-adhesive material comprises silicone elastomer.


The outer layer may also comprise non self-adhesive materials such as polyolefins (preferably polyethylene homopolymers of copolymers) but not to the extent that the self-adhesive properties are falling below 5 grams/15 mm measured by the method described below.


In another version, the outer layer may comprise tackifiers such as hydrocarbon resins, terpene resins, rosins and the like. Typical examples are Escorez materials from Exxon.


In a further preferred version the outer layer may comprise materials such as “substantially non resilient materials” (SNR). See the above definition of this term.


In a preferred version of the invention, the self-adhesive material in the outer layer is an extrudable material, meaning that it is melt processed by extrusion process.


As defined above, the phrase “outer 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.


Inner Layer


Preferred materials for the inner layer include polyolefins, such as low density polyethylene, high density polyethylene, ethylene ester copolymer, ethylene alpha olefin copolymer and polypropylene. Ionomers and styrene copolymers are also possible. Ethylene alpha olefin copolymer is particularly preferred.


According to a further embodiment, the present invention is of the same configuration where inner layer comprises a “substantially non resilient material” (SNR).


In a preferred version of the invention, the SNR material is at least 10 percent, preferably at least 20, preferably at least 30 percent per weight of the inner layer.


In a preferred version the inner layer comprises at least one release agent that is a polymer or chemical substance that allows the surface tension of the inner side to decrease. The reason for this is to allow the easy unwinding of the reel when the inner and the outer side come in contact one to the other.


Intermediate Layers


In the intermediate layers, also called adjacent layers, typical adhesive resins like maleic anhydrite modified polyolefins may be used. Typical examples are BYNEL® from Dupont and OREVAC® from Arkema.


In another preferred version of the invention, polyamide could be used as intermediate layer.


General


The preferred production method for the film is the hot blown film method, which is well known in the art. Other methods like extrusion through flat cast die are also possible.


Additives well known in the art may be used in one or more layers of the present invention. Slip additives, antiblock additives, antifog, polymer processing aids may be used if pertinent. Antimicrobial additives may also be used in one or more of the layers to inhibit the microbe formation. Preferably the antimicrobial is put on the side where the waste is in direct vicinity.


In order to increase the mechanical properties the film may be crosslinked with one of the following methods:


E-beam radiation, gamma radiation, moisture crosslinking using silane grafting compounds, peroxide crosslinking.


The film may be in tubular form or sealed at the edges or single sheet configuration. Centerfold configuration is also possible.


In a preferred version the film tears easily along the transverse direction. Even if the tear is initiated by an operator along the MD, then a further propagation leads the tear along the transverse direction.


EXAMPLES
Example 1

A 5 layer film is produced in a commercial hot blown film line with the following recipe:















Inner layer,
80% EAO1 + 15% SNR1 + 5% ADDITIVES


Adjacent layer
100% ADH 1


Barrier layer
EVOH 1


Adjacent layer
100% ADH1


Outer layer
Ethylene vinyl acetate copolymer comprising 80% vinyl



acetate per weight (= a blend of EVA with 90%



vinyl acetate + 10% low density polyethylene)









See table 1


The thickness of the structure is 5/1.5/1.5/1.5/4 starting from the inner and going to the outer layer.













TABLE 1









Density



Type
Description
g/cm3




















EAO1
Ethylene octene copolymer
0.92



SNR1
Calcium carbonate compound
1.6



ADH1
LLDPE mod.
0.92




Adhesive tie



EVOH 1
EVOH with 32% ethylene
1.19










The weight per surface ratio of the film is 15.2 g/m2.


Example 2

A 5 layer film is produced in a hot blown film commercial line with the following recipe


















Inner layer,
80% EAO1 + 15% SNR1 + 5% ADDITIVES



Adjacent layer
100% ADH 1



Barrier layer
EVOH 1



Adjacent layer
100% ADH1



Outer layer
Propylene ethylene copolymer










The thickness of the structure is 5/1.5/1.5/1.5/3 starting from the inner and going to the outer layer.


The weight per surface ratio of the material is 13.2 g/m2.


Example 3

A 5 layer film is produced in a commercial hot blown film line with the following recipe


















Inner layer
80% EAO1 + 15% SNR1 + 5% ADDITIVES



Adjacent layer
100% ADH 1



Barrier layer
EVOH 1



Adjacent layer
100% ADH1



Outer layer
A blend of 90% ethylene vinyl acetate copolymer




comprising 80% vinyl acetate per weight + 10%




calcium carbonate polyethylene compound










See table 1


The thickness of the structure is 5/1.5/1.5/1.5/4 starting from the inner and going to the outer layer.


Example 4

A 5 layer film is produced in a hot blown film commercial line with the following recipe


















Inner layer
80% EAO1 + 15% SNR1 + 5% ADDITIVES



Adjacent layer
100% ADH 1



Barrier layer
EVOH 1



Adjacent layer
100% ADH1



Outer layer
Styrene butadiene styrene copolymer










The thickness of the structure is 5/1.5/1.5/1.5/3 starting from the inner and going to the outer layer.


The weight per surface ratio of the material is 13.2 g/m2.


Tests






    • 1. Tensile strength and elongation test is done according to ASTM D 882.

    • 2. Odor test is done in the following way.


      Test 1.

    • Tensile strength and elongation is measured as per ASTM D882.

    • MD stands for machine direction, whereas TD stands for transverse direction.




















TENSILE
ELONG-
TENSILE
ELONG-



STRENGTH
ATION
STRENGTH
ATION


EXAMPLE
(MD)
(MD)
(TD)
(TD)



















1
25.5
110
23.5
430


2
27.2
104
24.3
430


3
26
160
16
400


4
22
180
18
505










Odor Testing


10 soiled diapers are put in a film of the present invention and also in a commercially sold film. The commercially sold film is believed to be monolayer.


The packs are put in PVDC comprising bags, so the odor cannot escape during the time of the evaluation.


The bags are opened 3 days after the soiling of the diapers and smell was evaluated by a 5 member panel.


The packs made from examples 1-4 were found substantially less smelly than the commercially sold ones.


Adhesive Property Testing


Films of examples 1, 2, 3, 4 were tested as per adhesive property as follows:


Two pieces of dimensions 100×1500 mm film are cut by the operator. Then the operator places them under the jaw of a TOSS sealing machine under temperature 20° C. The pressure of the jaws is 3 bar. Contact (sealing time) of the two pieces of the film is 5 seconds. The self-adhesive side of the first piece is bonded to the self-adhesive side of the second piece.


Then 15 mm stripes are cut either along the MD (machine direction) or along the TD (transverse direction). The adhesive force is measured in an Instron® Instron machine as per the methodology of ASTM D882.


According to this test the self-adhesive force is


Example 1, 15 grams


Example 2, 11 grams


Example 3, 115 grams


Example 4, 80 grams


The above numbers are averages of the measurements along the MD and TD direction. A commercially used film tested as per adhesive property gave practically a self-adhesive force of 0 grams therefore it could not be potentially used in the application.


Tear Test


It was noticed that when a human operator tears the film along the machine direction then a further propagation of the tear follows the transverse direction. This unexpected controlled tear property can be useful in various applications.

Claims
  • 1. A multilayer film having a weight per surface ratio of less than 25 g/m2 for use in malodorous item packaging, where the film comprises at least an outer layer comprising a self-adhesive material and a layer comprising an oxygen barrier material; where the layer comprising the self-adhesive material is configured to be in direct contact with an item packed in the film when the film is in use for packaging and wherein the self-adhesive material comprises a material selected from the group consisting of an ethylene vinyl acetate copolymer where the vinyl acetate weight ratio is at least 20%, an ethylene vinyl acetate copolymer where the vinyl acetate weight ratio is at least 25%, an ethylene vinyl acetate copolymer where the vinyl acetate weight ratio is at least 30%, an ethylene vinyl acetate copolymer where the vinyl acetate weight ratio is at least 40%, a propylene ethylene copolymer where the ethylene content is at least 10% per weight, styrene copolymers with a styrene content of less than 50% per weight, an ethylene alpha olefin copolymer with a density less than 0.9 g/cm3, a maleic anhydrite grafted polyolefin, an ethylene methyl acrylate copolymer with a methyl acrylate content of at least 20%, an ethylene butyl acrylate material with a butyl acrylate content of at least 15%, a poly-isobutylene polymer (PIB), a polybutene copolymer, a silicone elastomer, and mixtures thereof.
  • 2. The film of claim 1, where the weight per surface ratio of the film is less than 20 g/m2.
  • 3. The film of claim 1, where the weight per surface ratio of the film is less than 15 g/m2.
  • 4. The film of claim 1, where the film comprises or consists of the structure: OUTER LAYER/ABUSE LAYER/INTERMEDIATE LAYER/BARRIER LAYER/INTERMEDIATE LAYER/ABUSE LAYER/INNER LAYER.
  • 5. The film of claim 1, where the film comprises or consists of the structure: OUTER LAYER/INTERMEDIATE LAYER/BARRIER LAYER/INTERMEDIATE LAYER/INNER LAYER.
  • 6. The film of claim 1, where the self-adhesive material comprises ethylene vinyl acetate copolymer, where the vinyl acetate weight ratio is at least 20%.
  • 7. The film of claim 1, where the self-adhesive material comprises ethylene vinyl acetate copolymer, where the vinyl acetate weight ratio is at least 25%.
  • 8. The film of claim 1, where the self-adhesive material comprises ethylene vinyl acetate copolymer, where the vinyl acetate weight ratio is at least 30%.
  • 9. The film of claim 1, where the self-adhesive material comprises ethylene vinyl acetate copolymer, where the vinyl acetate weight ratio is at least 40%.
  • 10. The film of claim 1, where the self-adhesive material comprises a propylene ethylene copolymer where the ethylene content is at least 10% per weight, or an ethylene alpha olefin copolymer with density less than 0.9 g/cm3, ora maleic anhydrite grafted polyolefin, orstyrene copolymers with styrene content less than 50% per weight, oran ethylene methyl acrylate copolymer with a methyl acrylate content of at least 20%, oran ethylene butyl acrylate material with a butyl acrylate content of at least 15%, ora poly-isobutylene polymer (PIB) or a polybutene copolymer, ora silicone elastomer,or mixtures thereof.
  • 11. The film of claim 10, where the self-adhesive material comprises an ethylene alpha olefin copolymer with a density less than 0.880 g/cm3.
  • 12. The film of claim 1, where the barrier layer comprises EVOH, polyamide or mixtures thereof.
  • 13. The film of claim 1, where the film comprises an inner layer comprising a polyolefin.
  • 14. The film of claim 13, where the inner layer comprises an ethylene alpha olefin copolymer.
  • 15. The film of claim 1, where the film comprises an inner layer comprising a substantially non resilient material.
  • 16. A multilayer film having a weight per surface ratio of less than 25 g/m2 for use in malodorous item packaging, where the film comprises at least an outer layer comprising a self-adhesive material; a layer comprising an oxygen barrier material; and an inner layer comprising a substantially non resilient material, wherein the self-adhesive material is selected from the group consisting of an ethylene vinyl acetate copolymer where the vinyl acetate weight ratio is at least 20%, an ethylene vinyl acetate copolymer where the vinyl acetate weight ratio is at least 25%, an ethylene vinyl acetate copolymer where the vinyl acetate weight ratio is at least 30%, an ethylene vinyl acetate copolymer where the vinyl acetate weight ratio is at least 40%, a propylene ethylene copolymer where the ethylene content is at least 10% per weight, and a styrene copolymer with a styrene content of less than 50% per weight.
Priority Claims (1)
Number Date Country Kind
12154500 Feb 2012 EP regional
US Referenced Citations (155)
Number Name Date Kind
2380054 Lautmann Aug 1943 A
2376185 Randall May 1945 A
3214884 Langdon Nov 1965 A
3299194 Golike Jan 1967 A
3356192 Cameron Dec 1967 A
3456044 Pahlke Jul 1969 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
4207363 Lustig Jun 1980 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
4857399 Vicik Aug 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
5382470 Vicik Jan 1995 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
6610046 Usami et al. Aug 2003 B1
6663905 Ennis et al. Dec 2003 B1
6682792 Schmal et al. Jan 2004 B2
6777046 Tatarka et al. Aug 2004 B1
6869686 Idlas Mar 2005 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
9290320 Gkinosatis Mar 2016 B2
9365687 Gkinosatis Jun 2016 B2
20020038535 Jensen et al. Apr 2002 A1
20020066261 Richards Jun 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
20040020913 Hovorka 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
20040159972 Koschmieder et al. 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
20090196962 Gkinosatis Aug 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
20130227916 Gkinosatis Sep 2013 A1
20150010764 Gkinosatis Jan 2015 A1
20150210454 Gkinosatis Jul 2015 A1
20160176612 Ginosatis Jun 2016 A1
Foreign Referenced Citations (58)
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
0 627 465 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
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
WO 9712758 Apr 1997 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 (124)
Entry
Interview Summary corresponding to U.S. Appl. No. 11/801,609 dated Jul. 31, 2012.
Official Action corresponding to U.S. Appl. No. 12/150,168 dated Aug. 14, 2012.
Official Action corresponding to U.S. Appl. No. 12/319,149 dated Aug. 27, 2012.
Official Action corresponding to U.S. Appl. No. 12/319,150 dated Mar. 14, 2013.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Jan. 17, 2012.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Sep. 25, 2012.
Unisource—Moisture Barrier & Oxygen Barrier Transmission Rates; <http://www.unisourcelink.com/packaging/pdf/MoistureBarrier.pdf> (Retrieved on Jan. 10, 2012).
“Baymod L 2450,” Product Data Sheet, LANXESS. (2 pages) (2007).
“Elvaloy resins,” Product Data Sheet, DuPont Packaging & Industrial Polymers. (2 pages) (2010).
Interview Summary corresponding to U.S. Appl. No. 12/319,150 dated Sep. 6, 2013.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Jul. 24, 2013.
“15.13xEA—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.
“Polybutylene terephthalate,” Britannica Online Encyclopedia. pp. 1-3 (Accessed on Sep. 7, 2011) <http://www.britannica.com/EBchecked/topic/468341/polybuylene-terephthalate-PBT>.
“Polybutylene terephthalate (PBT),” 1 page <http://www.britannica.com/EBchecked/topic/468341/polybutylene-terephthalate-PBT> (Accessed on Jun. 13, 2012).
“Polymer Blend,” IUPAC Compendium of Chemical Terminology. 2nd Edition (1997).
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 D 882-09. Standard Test Method for Tensile Properties of Thin Plastic Sheeting. American National Standards Institute. Jan. 2009. www.astm.org.
ASTM D 1003-07 “Haze and Luminous Transmittance of Transparent Plastics,” ASTM International. pp. 1-7.
ASTM D 1525-07 “Vicat Softening Temperature of Plastics,” ASTM International. pp. 1-9.
ASTM D 2732-03 “Unrestrained Linear Thermal Shrinkage of Plastic Film and Sheeting,” ASTM International. pp. 1-5.
ASTM D 3418-08. 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 D 3985. 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.
ASTM F 1927-07. 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.
BS 2782-0:2004 “Methods of Testing Plastics,” British Standards Institution. pp. 1-29 (2004).
English abstract of JP 2005-103902, USUI, Apr. 2005.
European Search Report corresponding to European Patent Application No. 08173056.6-2109 dated Mar. 16, 2009.
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. 08154742.4-2124 dated Jul. 2, 2009.
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.
Extended European Search Report corresponding to European Patent Application No. 10193414.9-1217 dated May 9, 2011.
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 Dec. 28, 2010.
Interview Summary corresponding to U.S. Appl. No. 12/150,261 dated Sep. 21, 2011.
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 Oct. 17, 2011.
Interview Summary corresponding to U.S. Appl. No. 12/319,149 dated Jun. 15, 2012.
Interview Summary corresponding to U.S. Appl. No. 12/319,150 dated Sep. 23, 2011.
Interview Summary corresponding to U.S. Appl. No. 12/322,347 dated Sep. 21, 2011.
Interview Summary corresponding to U.S. Appl. No. 12/508,233 dated Apr. 26, 2012.
Kipp, “Plastic Material Data Sheets,” MatWeb (2004) (5 pages).
Machine Translation of JP 2005-103902, USUI, Apr. 2005.
Notice of Allowance corresponding to U.S. Appl. No. 11/528,741 dated Oct. 28, 2011.
Official Action corresponding to U.S. Appl. No. 11/528,741 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. 11/528,741 dated May 18, 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. 11/801,609 dated Jun. 20, 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 Feb. 16, 2011.
Official Action corresponding to U.S. Appl. No. 12/150,168 dated Sep. 23, 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. 12/150,261 dated Mar. 22, 2011.
Official Action corresponding to U.S. Appl. No. 12/150,261 dated Jan. 31, 2012.
Official Action corresponding to U.S. Appl. No. 12/154,662 dated Mar. 29, 2011.
Official Action corresponding to U.S. Appl. No. 12/154,662 dated Aug. 18, 2011.
Official Action corresponding to U.S. Appl. No. 12/154,662 dated Jan. 18, 2012.
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. 12/319,149 dated Mar. 22, 2011.
Official Action corresponding to U.S. Appl. No. 12/319,149 dated Dec. 2, 2011.
Official Action corresponding to U.S. Appl. No. 12/319,150 dated Oct. 15, 2010.
Official Action corresponding to U.S. Appl. No. 12/319,150 dated Apr. 26, 2011.
Official Action corresponding to U.S. Appl. No. 12/319,150 dated Nov. 4, 2011.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated Sep. 14, 2010.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated Mar. 16, 2011.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated Oct. 26, 2011.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated May 15, 2012.
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 Mar. 9, 2011.
Official Action corresponding to U.S. Appl. No. 12/508,233 dated Nov. 23, 2011.
Official Action corresponding to U.S. Appl. No. 12/508,233 dated Jun. 6, 2012.
Official Action corresponding to U.S. Appl. No. 12/512,361 dated Aug. 31, 2011.
Official Action corresponding to U.S. Appl. No. 12/512,361 dated May 2, 2012.
Petrie, “Handbook of Adhesives and Sealants,” 2nd Edition. McGraw-Hill: New York, New York. pp. 465-466 (2007).
Search Report corresponding to French Patent Application No. 1059997 dated Jan. 16, 2012.
Official Action corresponding to U.S. Appl. No. 12/150,168 dated Apr. 26, 2013.
“Filling and sealing of containers” in Fellows, P.J. (2000). Food Processing Technology—Principles and Practice (2nd Edition). Woodhead Publishing.
Advisory Action corresponding to U.S. Appl. No. 12/319,150 dated Nov. 13, 2013.
Notice of Allowance corresponding to U.S. Appl. No. 12/150,168 dated Nov. 25, 2013.
Official Action corresponding to New Zealand Patent Application No. 626181 dated Jun. 18, 2014.
Official Action corresponding to United Kingdom Patent Application No. GB1020302.4 dated Jul. 2, 2014.
Official Action corresponding to U.S. Appl. No. 13/157,876 dated Nov. 19, 2013.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Nov. 29, 2013.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Apr. 24, 2014.
Official Action corresponding to U.S. Appl. No. 13/157,876 dated Jun. 2, 2014.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated Aug. 1, 2014.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Sep. 24, 2014.
Official action corresponding to European Patent Application No. 10 193 414.9-1303 dated Oct. 29, 2014.
Official Action corresponding to United Kingdom Patent Application No. GB1020302.4 dated Dec. 11, 2014.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Jan. 7, 2015.
Official Action corresponding to U.S. Appl. No. 13/523,462 dated Jan. 30, 2015.
Official Action corresponding to U.S. Appl. No. 13/157,876 dated Mar. 3, 2015.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated May 20, 2015.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Jun. 12, 2015.
Official Action corresponding to U.S. Appl. No. 13/682,160 dated Jun. 15, 2015.
Notice of Allowance corresponding to U.S. Appl. No. 13/157,876 dated Nov. 12, 2015.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Feb. 2, 2016.
Official Action corresponding to U.S. Appl. No. 12/319,150 dated Jul. 22, 2015.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Sep. 16, 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. 14/612,175 dated Dec. 9, 2015.
Advisory Action corresponding to U.S. Appl. No. 11/801,609 dated Jun. 16, 2016.
Notice of Allowance correspoding to U.S. Appl. No. 12/319,150 dated Feb. 12, 2016.
Notice of Allowance corresponding to U.S. Appl. No. 13/523,462 dated May 16, 2016.
Official Action corresponding to U.S. Appl. No. 12/322,347 dated Feb. 18, 2016.
Official Action corresponding to U.S. Appl. No. 12/957,947 dated Mar. 31, 2016.
Official Action corresponding to U.S. Appl. No. 13/682,160 dated Jun. 30, 2016.
Office Action corresponding U.S. Appl. No. 14/304,101 dated Jun. 30, 2016.
“Polymer Materials Selection for Radiation-Sterilized Products.” <http://www.mddionline.com/article/polymer-materials-selection-radiation-sterilized-products> dated Feb. 1, 2000.
Advisory Action, Examiner Initiated Interview Summary, and AFCP 2.0 Decision corresponding to U.S. Appl. No. 14/612,175 dated Jan. 4, 2017.
Interview Summary corresponding to U.S. Appl. No. 13/682,160 dated Oct. 28, 2016.
Notice of Decision form Post-Prosectuion Pilot Program (P3) Conference corresponding to U.S. Appl. No. 12/957,947 dated Dec. 14, 2016.
Official Action corresponding to U.S. Appl. No. 11/801,609 dated Nov. 16, 2016.
Official Action corresponding to U.S. Appl. No. 14/304,101 dated Dec. 9, 2016.
Related Publications (1)
Number Date Country
20130209797 A1 Aug 2013 US