AU1988697A - Creation of Inventions and Patents with Artificial Intelligence

AU1988697A – Zeolite in packaging film
– Google Patents

AU1988697A – Zeolite in packaging film
– Google Patents
Zeolite in packaging film

Info

Publication number
AU1988697A

AU1988697A
AU19886/97A
AU1988697A
AU1988697A
AU 1988697 A
AU1988697 A
AU 1988697A
AU 19886/97 A
AU19886/97 A
AU 19886/97A
AU 1988697 A
AU1988697 A
AU 1988697A
AU 1988697 A
AU1988697 A
AU 1988697A
Authority
AU
Australia
Prior art keywords
film
layer
zeolite
oxygen
article
Prior art date
1996-03-07
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.)

Granted

Application number
AU19886/97A
Other versions

AU727948B2
(en

AU727948C
(en

Inventor
Thomas A. Blinka
Frank B. Edwards
Nathanael R. Miranda
Drew V. Speer
Jeffrey A. Thomas
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.)

Cryovac LLC

Original Assignee
Cryovac LLC
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.)
1996-03-07
Filing date
1997-03-07
Publication date
1997-09-22
Family has litigation

First worldwide family litigation filed
litigation
Critical
https://patents.darts-ip.com/?family=27086752&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AU1988697(A)
“Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1997-03-07
Application filed by Cryovac LLC
filed
Critical
Cryovac LLC

1997-03-07
Priority claimed from US08/812,637
external-priority
patent/US5834079A/en

1997-09-22
Publication of AU1988697A
publication
Critical
patent/AU1988697A/en

2001-01-04
Publication of AU727948B2
publication
Critical
patent/AU727948B2/en

2003-03-14
Priority to AU2003201319A
priority
Critical
patent/AU2003201319B2/en

2005-10-27
Application granted
granted
Critical

2005-10-27
Publication of AU727948C
publication
Critical
patent/AU727948C/en

2017-03-07
Anticipated expiration
legal-status
Critical

Status
Expired
legal-status
Critical
Current

Links

Espacenet

Global Dossier

Discuss

Classifications

B—PERFORMING OPERATIONS; TRANSPORTING

B32—LAYERED PRODUCTS

B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM

B32B27/00—Layered products comprising a layer of synthetic resin

B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives

A—HUMAN NECESSITIES

A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE

A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES

A61L33/00—Antithrombogenic treatment of surgical articles, e.g. sutures, catheters, prostheses, or of articles for the manipulation or conditioning of blood; Materials for such treatment

A61L33/06—Use of macromolecular materials

A61L33/068—Use of macromolecular materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds

B—PERFORMING OPERATIONS; TRANSPORTING

B32—LAYERED PRODUCTS

B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM

B32B27/00—Layered products comprising a layer of synthetic resin

B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material

B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin

C—CHEMISTRY; METALLURGY

C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON

C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS

C08G83/00—Macromolecular compounds not provided for in groups C08G2/00 – C08G81/00

C08G83/007—Polyrotaxanes; Polycatenanes

C—CHEMISTRY; METALLURGY

C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON

C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients

C08K3/00—Use of inorganic substances as compounding ingredients

C08K3/34—Silicon-containing compounds

C08K3/36—Silica

C—CHEMISTRY; METALLURGY

C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON

C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients

C08K5/00—Use of organic ingredients

C08K5/0008—Organic ingredients according to more than one of the “one dot” groups of C08K5/01 – C08K5/59

C—CHEMISTRY; METALLURGY

C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON

C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS

C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers

C08L71/02—Polyalkylene oxides

B—PERFORMING OPERATIONS; TRANSPORTING

B32—LAYERED PRODUCTS

B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM

B32B2439/00—Containers; Receptacles

B—PERFORMING OPERATIONS; TRANSPORTING

B32—LAYERED PRODUCTS

B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM

B32B2581/00—Seals; Sealing equipment; Gaskets

Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T428/00—Stock material or miscellaneous articles

Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]

Y10T428/131—Glass, ceramic, or sintered, fused, fired, or calcined metal oxide or metal carbide containing [e.g., porcelain, brick, cement, etc.]

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T428/00—Stock material or miscellaneous articles

Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]

Y10T428/1334—Nonself-supporting tubular film or bag [e.g., pouch, envelope, packet, etc.]

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T428/00—Stock material or miscellaneous articles

Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]

Y10T428/1334—Nonself-supporting tubular film or bag [e.g., pouch, envelope, packet, etc.]

Y10T428/1341—Contains vapor or gas barrier, polymer derived from vinyl chloride or vinylidene chloride, or polymer containing a vinyl alcohol unit

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T428/00—Stock material or miscellaneous articles

Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]

Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T428/00—Stock material or miscellaneous articles

Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]

Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]

Y10T428/1355—Elemental metal containing [e.g., substrate, foil, film, coating, etc.]

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T428/00—Stock material or miscellaneous articles

Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]

Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]

Y10T428/1355—Elemental metal containing [e.g., substrate, foil, film, coating, etc.]

Y10T428/1359—Three or more layers [continuous layer]

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T428/00—Stock material or miscellaneous articles

Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]

Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]

Y10T428/1379—Contains vapor or gas barrier, polymer derived from vinyl chloride or vinylidene chloride, or polymer containing a vinyl alcohol unit

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T428/00—Stock material or miscellaneous articles

Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]

Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]

Y10T428/1397—Single layer [continuous layer]

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T428/00—Stock material or miscellaneous articles

Y10T428/249921—Web or sheet containing structurally defined element or component

Y10T428/249953—Composite having voids in a component [e.g., porous, cellular, etc.]

Y10T428/249955—Void-containing component partially impregnated with adjacent component

Y10T428/249956—Void-containing component is inorganic

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T428/00—Stock material or miscellaneous articles

Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer

Y10T428/2813—Heat or solvent activated or sealable

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T428/00—Stock material or miscellaneous articles

Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer

Y10T428/2813—Heat or solvent activated or sealable

Y10T428/2817—Heat sealable

Y10T428/2826—Synthetic resin or polymer

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T428/00—Stock material or miscellaneous articles

Y10T428/31504—Composite [nonstructural laminate]

Y10T428/31855—Of addition polymer from unsaturated monomers

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T428/00—Stock material or miscellaneous articles

Y10T428/31504—Composite [nonstructural laminate]

Y10T428/31855—Of addition polymer from unsaturated monomers

Y10T428/31909—Next to second addition polymer from unsaturated monomers

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T428/00—Stock material or miscellaneous articles

Y10T428/31504—Composite [nonstructural laminate]

Y10T428/31855—Of addition polymer from unsaturated monomers

Y10T428/31909—Next to second addition polymer from unsaturated monomers

Y10T428/31913—Monoolefin polymer

Description

ZEOLITE IN PACKAGING FILM
FIELD OF THE INVENTION
The invention generally relates to compositions, articles and methods for scavenging by-products of an oxygen scavenging reaction.
BACKGROUND OF THE INVENTION
It is well known that limiting the exposure of an oxygen-sensitive product to oxygen maintains and enhances the quality and “shelf-life” of the product. In the food packaging industry, several means for regulating oxygen exposure have already been developed.
These means include modified atmosphere packaging (MAP) for modifying the interior environment of a package; gas flushing; vacuum packaging; vacuum packaging combined with the use of oxygen barrier packaging materials; etc. Oxygen barrier films and laminates reduce or retard oxygen permeation from the outside environment into the package interior.
Another method currently being used is through “active packag¬ ing.” The inclusion of oxygen scavengers within the cavity or interior of the package is one form of active packaging. Typically, such oxygen scavengers are in the form of sachets which contain a composition which scavenges the oxygen through chemical reactions. One type of sachet contains iron compositions which oxidize. Another type of sa¬ chet contains unsaturated fatty acid salts on a particulate adsorbent. Yet another type of sachet contains metal/ polyamide complex.
One disadvantage of sachets is the need for additional packaging operations to add the sachet to each package. A further disadvantage arising from the use of some sachets is that certain atmospheric condi¬ tions (e.g., high humidity, low CO2 level) in the package are required in order for scavenging to occur at an adequate rate.

Another means for limiting the exposure to oxygen involves incor¬ porating an oxygen scavenger into the packaging structure itself. This achieves a more uniform scavenging effect throughout the package. This may be specially important where there is restricted air circulation inside the package. In addition, such incorporation can provide a means of intercepting and scavenging oxygen as it passes through the walls of the package (herein referred to as an “active oxygen barrier”), thereby maintaining the lowest possible oxygen level throughout the package. One attempt to prepare an oxygen-scavenging wall involves the incorporation of inorganic powders and/or salts. However, incorpora¬ tion of these powders and/or salts causes degradation of the wall’s transparency and mechanical properties such as tear strength. In ad¬ dition, these compounds can lead to processing difficulties, especially in the fabrication of thin films, or thin layers within a film structure. Even further, the scavenging rates for walls containing these compounds are unsuitable for some commercial oxygen- scavenging applications, e.g. such as those in which sachets are employed.
Other efforts have been directed to incorporating a metal catalyst- polyamide oxygen scavenging system into the package wall. However, this system does not exhibit oxygen scavenging at a commercially fea¬ sible rate.
Oxygen scavengers suitable for commercial use in films of the present invention are disclosed in U.S. Patent No. 5,350,622, and a method of initiating oxygen scavenging generally is disclosed in U.S.
Patent No 5,21 1,875. Both applications are incorporated herein by ref¬ erence in their entirety. According to U.S. Patent No. 5,350,622, oxygen scavengers are made of an ethylenically unsaturated hydrocarbon and transition metal catalyst. The preferred ethylenically unsaturated hy- drocarbon may be either substituted or unsubstituted. As defined herein, an unsubstituted ethylenically unsaturated hydrocarbon is any

compound which possesses at least one aliphatic carbon-carbon double bond and comprises 100% by weight carbon and hydrogen. A substi¬ tuted ethylenically unsaturated hydrocarbon is defined herein as an ethylenically unsaturated hydrocarbon which possesses at least one aliphatic carbon-carbon double bond and comprises about 50% – 99% by weight carbon and hydrogen. Preferable substituted or unsubsti¬ tuted ethylenically unsaturated hydrocarbons are those having two or more ethylenically unsaturated groups per molecule. More preferably, it is a polymeric compound having three or more ethylenically unsatu- rated groups and a molecular weight equal to or greater than 1,000 weight average molecular weight.
Preferred examples of unsubstituted ethylenically unsaturated hydrocarbons include, but are not limited to, diene polymers such as polyisoprene, (e.g., trans-polyisoprene) and copolymers thereof, cis and trans 1,4-polybutadiene, 1,2-polybutadienes, (which are defined as those polybutadienes possessing greater than or equal to 50% 1 ,2 mi¬ cro structure), and copolymers thereof, such as styrene-butadiene co- polymer. Such hydrocarbons also include polymeric compounds such as polypentenamer, polyoctenamer, and other polymers prepared by cyclic olefin metathesis; diene oligomers such as squalene; and poly¬ mers or copolymers with unsaturation derived from dicyclopentadiene, norbornadiene, 5-ethylidene-2-norbornene, 5-vinyl-2-norbornene, 4- vinylcyclohexene, or other monomers containing more than one carbon- carbon double bond (conjugated or non-conjugated). Preferred substituted ethylenically unsaturated hydrocarbons in¬ clude, but are not limited to, those with oxygen -containing moieties, such as esters, carboxylic acids, aldehydes, ethers, ketones, alcohols, peroxides, and/ or hydroperoxides. Specific examples of such hydro¬ carbons include, but are not limited to, condensation polymers such as polyesters derived from monomers containing carbon-carbon double bonds, and unsaturated fatty acids such as oleic, ricinoleic, dehydrated

ricinoleic, and linoleic acids and derivatives thereof, e.g. esters. Such hydrocarbons also include polymers or copolymers derived from (meth)allyl (meth)acrylates. Suitable oxygen scavenging polymers can be made by trans-esterification. Such polymers are disclosed in WO 95/02616, incorporated herein by reference as if set forth in full. The composition used may also comprise a mixture of two or more of the substituted or unsubstituted ethylenically unsaturated hydrocarbons described above. While a weight average molecular weight of 1 ,000 or more is preferred, an ethylenically unsaturated hydrocarbon having a lower molecular weight is usable, provided it is blended with a film- forming polymer or blend of polymers.
As will also be evident, ethylenically unsaturated hydrocarbons which are appropriate for forming solid transparent layers at room tem¬ perature are preferred for scavenging oxygen in the packaging articles described above. For most applications where transparency is neces¬ sary, a layer which allows at least 50% transmission of visible light is preferred.
When making transparent oxygen-scavenging layers according to this invention, 1 ,2-polybutadiene is especially preferred for use at room temperature. For instance, 1,2-polybutadiene can exhibit transpar¬ ency, mechanical properties and processing characteristics similar to those of polyethylene. In addition, this polymer is found to retain its transparency and mechanical integrity even after most or all of its oxy¬ gen capacity has been consumed, and even when little or no diluent resin is present. Even further, 1,2-polybutadiene exhibits a relatively high oxygen capacity and, once it has begun to scavenge, it exhibits a relatively high scavenging rate as well.
When oxygen scavenging at low temperatures is desired, 1,4- polybutadiene, and copolymers of styrene with butadiene, and styrene with isoprene are especially preferred. Such compositions are disclosed in U.S. Patent No. 5,310,497 issued to Speer et al. on May 10, 1994

and incorporated herein by reference as if set forth in full. In many cases it may be desirable to blend the aforementioned polymers with a polymer or copolymer of ethylene.
Other oxygen scavengers which can be used in connection with this invention are disclosed in U.S. Patent Nos. 5, 075,362 (Hofeldt et al.), 5, 106,886 (Hofeldt et al.), 5, 204,389 (Hofeldt et al.), and 5, 227,41 1 (Hofeldt et al.), all incorporated by reference herein in their entirety. These oxygen scavengers include ascorbates or isoascorbates or mixtures thereof with each other or with a sulfite, often sodium sul- fite.
Still other oxygen scavengers which can be used in connection with this invention are disclosed in PCT patent publications WO 91 / 17044 (Zapata Industries) and WO94/09084 (Aquanautics Corpo¬ ration), both incorporated by reference herein in their entirety. These oxygen scavengers include an ascorbate with a transition metal cata¬ lyst, the catalyst being a simple metal or salt or a compound, complex or chelate of the transition metal; or a transition metal complex or chelate of a polycarboxylic or salicylic acid or polyamine, optionally with a reducing agent such as ascorbate, where the transition metal complex or chelate acts primarily as an oxygen scavenging composition.
Yet other oxygen scavengers which can be used in connection with this invention are disclosed in PCT patent publication WO 94/ 12590 (Commonwealth Scientific and Industrial Research Organi¬ sation), incorporated by reference herein in its entirety. These oxygen scavengers include at least one reducible organic compound which is reduced under predetermined conditions, the reduced form of the com¬ pound being oxidizable by molecular oxygen, wherein the reduction and /or subsequent oxidation of the organic compound occurs inde¬ pendent of the presence of a transition metal catalyst. The reducible organic compound is preferably a quinone, a photoreducible dye, or a carbonyl compound which has absorbence in the UV spectrum.

Sulfites, alkali metal salts of sulphites, and tannins, are also contemplated as oxygen scavenging compounds.
As indicated above, the ethylenically unsaturated hydrocarbon is combined with a transition metal catalyst. While not being bound by any particular theory, the inventors observe that suitable metal cata¬ lysts are those which can readily interconvert between at least two oxi¬ dation states. See Sheldon, R. A.; Kochi, J. K.; “Metal-Catalyzed Oxida¬ tions of Organic Compounds” Academic Press, New York 1981.
Preferably, the catalyst is in the form of a transition metal salt, with the metal selected from the first, second or third transition series of the Periodic Table. Suitable metals include, but are not limited to, manganese II or III, iron II or III, cobalt II or III, nickel II or III, copper I or II, rhodium II, III or IV, and ruthenium II or III. The oxidation state of the metal when introduced is not necessarily that of the active form. The metal is preferably iron, nickel or copper, more preferably manga¬ nese and most preferably cobalt. Suitable counterions for the metal include, but are not limited to, chloride, acetate, stearate, palmitate, caprylate, linoleate, tallate, 2 -ethylhexanoate, neodecanoate, oleate or naphthenate. Particularly preferable salts include cobalt (II) 2- ethylhexanoate and cobalt (II) neodecanoate. The metal salt may also be an ionomer, in which case a polymeric counterion is employed. Such ionomers are weli known in the art.
The ethylenically unsaturated hydrocarbon and transition metal catalyst can be further combined with one or more polymeric diluents, such as thermoplastic polymers which are typically used to form film layers in plastic packaging articles. In the manufacture of certain packaging articles well known thermosets can also be used as the polymeric diluent.
Polymers which can be used as the diluent include, but are not limited to, polyethylene terephthalate (PET), polyethylene, low or very low density polyethylene, ultra-low density polyethylene, linear low

density polyethylene, polypropylene, polyvinyl chloride, polystyrene, and ethylene copolymers such as ethylene-vinyl acetate, ethylene-alkyl (meth)acrylates, ethylene-(meth)acrylic acid and ethylene- (meth) acrylic acid ionomers. Blends of different diluents may also be used. However, as indicated above, the selection of the polymeric diluent largely de¬ pends on the article to be manufactured and the end use. Such selec¬ tion factors are well known in the art.
Further additives can also be included in the composition to im¬ part properties desired for the particular article being manufactured. Such additives include, but are not necessarily limited to, fillers, pig¬ ments, dyestuffs, antioxidants, stabilizers, processing aids, plasticizers, fire retardants, anti-fog agents, etc.
The mixing of the components listed above is preferably accom¬ plished by melt-blending at a temperature in the range of 50°C to 300°C. However alternatives such as the use of a solvent followed by evaporation may also be employed. The blending may immediately precede the formation of the finished article or preform or precede the formation of a feedstock or masterbatch for later use in the production of finished packaging articles. Although these technologies offers great potential in packaging applications, it has been found that oxygen scavenging structures can sometimes generate reaction byproducts which can affect the taste and smell of the packaged material (i.e. organoleptic properties), or raise food regulatory issues. These by-products can include acids, aldehydes and ketones.
The inventors have found that this problem can be minimized by the use of zeolites (such as organophilic zeolites) which absorb odor- causing reaction byproducts. The zeolites can be incorporated into one or more layers of a multilayer film or container which includes an oxy- gen scavenging layer. However, one of ordinary skill in the art will read¬ ily recognize that the present invention is applicable to any oxygen

scavenging system that produces by-products such as acids, aldehydes, and ketones.
DEFINITIONS “Film” (F) herein means a film, laminate, sheet, web, coating, or the like which can be used to package a product.
“Zeolite” herein refers to molecular sieves, including alumino- phosphates and aluminosilicates with a framework structure enclosing cavities occupied by large ions and/or water molecules, both of which have considerable freedom of movement permitting ion exchange and reversible dehydration. The framework may also contain other cations such as Mn, Ti, Co, and Fe. An example of such materials are the tita- nosilicate and titanoaluminosilicate molecular sieves. Unlike amor¬ phous materials, these crystalline structures contain voids of discrete size. A typical naturally occurring zeolite is the mineral faujasite with formula
Nai3Ca1 ιMg9K2Al55Si i37θ384-235H20.
Ammonium and alkylammonium cations may be incorporated in synthetic zeolites, e.g. NH4, CH3NH3, (CH3)2NH2, (CH3)3 H, and
(CH3)4N. Some zeolites have frameworks of linked truncated octahedra (Beta-cages) characteristic of the structure of sodalite. Numerous syn¬ thetic zeolites are available.
“Oxygen scavenger” (OS) and the like herein means a composi- tion, article or the like which consumes, depletes or reacts with oxygen from a given environment.
“Actinic radiation” and the like herein means any form of radia¬ tion, such as ultraviolet radiation or electron beam irradiation, dis¬ closed in U.S. Patent No. 5.21 1 ,875 (Speer et al.). “Polymer” and the like herein means a homopolymer, but also co¬ polymers thereof, including bispolymers, terpolymers, etc.

“Ethylene alpha-olefin copolymer” and the like herein means such heterogeneous materials as linear low density polyethylene (LLDPE), linear medium density polyethylene (LMDPE) and very low and ultra low density polyethylene (VLDPE and ULDPE); and homogeneous polymers such as metallocene catalyzed polymers such as EXACT (TM) materials supplied by Exxon, and TAFMER (TM) materials supplied by Mitsui Pet¬ rochemical Corporation. These materials generally include copolymers of ethylene with one or more comonomers selected from C4 to C JO a^_ pha-olefins such as butene- 1 (i.e., 1-butene), hexene- 1 , octene- 1 , etc. in which the molecules of the copolymers comprise long chains with rela¬ tively few side chain branches or cross-linked structures. This molecu¬ lar structure is to be contrasted with conventional low or medium density polyethylenes which are more highly branched than their re¬ spective counterparts. Other ethylene /alpha-olefin copolymers, such as the long chain branched homogeneous ethylene /alpha-olefin copoly¬ mers available from the Dow Chemical Company, known as AFFINITY (TM) resins, are also included as another type of ethylene alpha-olefin copolymer useful in the present invention.
As used herein, the term “polyamide” refers to polymers having amide linkages along the molecular chain, and preferably to synthetic polyamides such as nylons. Furthermore, such term encompasses both polymers comprising repeating units derived from monomers, such as caprolactam, which polymerize to form a polyamide, as well as copoly¬ mers of two or more amide monomers, including nylon terpolymers, also referred to generally as “copoly amides” herein.
“LLDPE” herein means linear low density polyethylene, which is an ethylene alpha olefin copolymer.
“EVOH” herein means ethylene vinyl alcohol copolymer. “EVA” herein means ethylene vinyl acetate copolymer.

SUMMARY OF THE INVENTION
In one aspect of the invention, an article of manufacture com¬ prises an oxygen scavenger and a zeolite. In a second aspect of the invention, a package comprisesan arti¬ cle and a container into which the oxygen sensitive article is disposed, the container including a component comprising an oxygen scavenger and a zeolite.
In a third aspect of the invention, a method of making an article of manufacture having reduced migration of by-products of an oxygen scavenging reaction comprises providing an article comprising an oxy¬ gen scavenger and a zeolite and exposing the article to actinic radiation.
BRIEF DESCRIPTION OF THE DRAWINGS The invention may be further understood with reference to the drawings wherein Figures 1 through 5 are schematic cross-sections of various embodiments of a film of the present invention.
DESCRIPTION OF THE PREFERRED EMBODIMENTS The invention can be used to make various articles of manufac¬ ture, compounds, compositions of matter, coatings, etc. Two preferred forms are sealing compounds, and flexible films, both useful in packag¬ ing of food and non-food products.
It is known to use sealing compounds in the manufacture of gas- kets for the rigid container market. Large, wide diameter gaskets are typically made using a liquid plastisol. This plastisol is a highly vis¬ cous, liquid suspension of polymer particles in a plasticizer. In the manufacture of metal or plastic caps, lids, and the like, this liquid plastisol is applied to the annulus of a container such as a jar, and the container with the applied plastisol is “fluxed” in an oven to solidify the

plastisol into a gasket. The result is a gasket formed around the annu- lus of the container.
Smaller gaskets are typically made for use in beer crowns in bot¬ tles. A polymer melt is applied by cold molding to the entire inner sur- face of the crown. Both PVC and other polymers are used in this appli¬ cation.
Discs for plastic caps are typically made by taking a ribbon of gasket material and making discs, and inserting the discs into the plastic cap. In all of these applications, the use of an oxygen scavenger and zeolite beneficially provides removal of oxygen from the interior envi¬ ronment of the container, while controlling undesirable by-products of the oxygen scavenging reaction.
Thus, a gasket includes a polymeric composition, an oxygen scav- enger, and a zeolite. The gasket adheres a metal or plastic lid or clo¬ sure to a rigid or semi-rigid container, thus sealing the lid or closure to the container.
Referring to Figure 1, a multilayer film 10 is shown, having layer 12 and layer 14. Figure 2 shows a multilayer film with layers 12, 14, and 16. Lay¬ ers 12, 14, and 16 are preferably polymeric.
Layer 12 comprises a zeolite. Preferred materials are the molecu¬ lar sieves of the type disclosed in U.S. Patent No. 4,795,482 (Gioffre et al.), incorporated herein by reference in its entirety. Also useful in the present invention are zeolites supplied by the Davison division of
W.R.Grace & Co. -Conn. Preferred particle sizes for zeolites used in the present invention are between 0.1 and 10 micrometers, and more pref¬ erably between 0.5 and 3 micrometers.
Layer 14 comprises an oxygen scavenger, preferably a polymeric oxygen scavenger, more preferably one of the materials described above.

Layer 16 comprises an oxygen barrier material, such as ethylene vinyl alcohol copolymer (EVOH), Saran (vinylidene chloride copolymer), polyester, polyamide, metal, silica coating, etc.
Figure 3 shows a laminated film in which a three layer film is ad- hered to a second film. Layers 32, 34, and 36 correspond functionally and compositionally to 12, 14, and 16 respectively of Figure 2, and layer 38 is an intermediate layer which can comprise any polymeric material such as polyolefin, more preferably ethylenic polymers such as ethylene/ alpha-olefin and ethylene/ unsaturated ester copolymers, more preferably ethylene /vinyl acetate copolymer. Layer 31 represents a conventional adhesive such as polyurethane adhesive. Comparative 2 in Table 6 exemplifies the laminated film of Figure 3.
Figure 4 shows a laminated film in which a four layer film is ad¬ hered to a second film. Layers 42, 44, 46 and 48 correspond function – ally and compositionally to layers 32, 34, 36 and 38 respectively of Fig¬ ure 3. Layer 49 is an innermost heat sealable layer which can comprise any polymeric material such as polyolefin, more preferably ethylenic polymers such as ethylene /alpha-olefin and ethyene/ unsaturated ester copolymers, such as ethylene vinyl acetate copolymer. Layer 46 pro- vides oxygen barrier to the film structure, and adheres to layer 48 by means of conventional adhesive 41. This adhesive corresponds to layer 31 of Figure 3, and is shown simply as a thickened line. Examples 2 and 3 of Table 6 exemplify the laminated film of Figure 4.
Figure 5 shows a nine layer film. Example 1 and Comparative 1 in Table 2 exemplify the film of Figure 5.
Layer 57 is an abuse-resistant layer useful as an outermost layer of a film when used in a packaging application.
Layers 54 and 56 correspond functionally and compositionally to layers 14 and 16 respectively of Figures 2 and 3, as well as to layers 44 and 46 respectively of Figure 4.

Layers 52, 53, 58 and 59 comprise an adhesive. The adhesive is preferably polymeric, more preferably acid or acid anhydride-grafted polyolefins. In addition, these layers can comprise a zeolite.
Layer 55 comprises a heat resistant material. This can be any suitable polymeric material, preferably an amide polymer such as nylon 6, or a polyester such as polyethylene terephthalate.
Layer 51 comprises a heat sealable material. This can be any suitable polymeric material, preferably an olefinic polymer such as an ethylenic polymer, more preferably an ethylene alpha olefin copolymer. In addition, layer 51 can further comprise a zeolite.
The invention may be further understood by reference to the ex¬ amples shown below. Table 1 identifies the materials used in the ex¬ amples. The remaining tables describe the films made with these mate¬ rials, and organoleptic or migration data resulting from testing some of these films.
TABLE 1

SUBSTrrUTE SHEET (RULE 26)

Certain materials were blended together for some of the film structures, and these blends are identified as follows: PEB i = 90% PEi + 10% AB j .
PEB2 = 90% PEi + 10% PEB3. PEB3 = 80% PE3 + 20% PE4.
PPBi = 60% PPi + 40% EBi .
PPB = 40% PPi + 60% EB i .
OSBi = 76.5% OSi + 13.5% OS2 + 9.2% EVi + 0.5% PI j + 0.3% TCi.
OSB2 = 50% OS3 + 40% PE3 + 8.54% EVi + 0.90% TC ι+ 0.50% PI j + 0.05% calcium oxide + 0.01% antioxidant (Irganox 1076).
OSB3 = 60% OS + 38.83% EV3 + 1.06% TC2 + 0.10% PI2 + 0.01% antioxidant (Irganox 1076).
OSB4 = 40% OS3 + 58.83% EV3 + 1.06% TC2 + 0. 10% PI2 + 0.01% antioxidant (Irganox 1076). ZB i = 87% PEi + 10% AB i + 3% Z .
ZB2 = 90% PE2 + 10% Zi .
ZB3 = 90% PE2 + 10% Z2.
ZB4 = 90% PE + 6% PE3 + 2% PE4 + 1% Z3 + 1% Z4
ZB5 = 80% PE2 + 20% Z2. ZB6 = 80% PE3 + 20% Z2.
In Table 2, a nine-layer film structure in accordance with the in¬ vention, and a comparative film, are disclosed. These were each made by coextrusion of the layers.
TABLE 2

The target (and approximate actual) gauge (in mils) of each layer of the nine-layer film is shown below. Layer 9 would preferably form the food or product contact layer in a typical packaging application.

The films of Example 1 and Comparative 1 were subjected to food law migration tests to evaluate whether zeolites could reduce the con¬ centration of extractables. The films were triggered by ultraviolet light according to the procedure disclosed in U.S. Patent No 5,21 1 ,875. The films were converted into 280 cm2 pouches and the pouches were filled with a food simulant. The filled pouches were then retorted at 100°C for 30 minutes and stored at 50°C for 10 days. The food simulant was decanted from the pouches and analyzed. Table 3 shows a list of po¬ tential extractables. Table 4 shows the concentration of the same ex¬ tractables, where the films were extracted with 8% ethanol solution as the food simulant. Table 5 shows the concentration of the same ex¬ tractables, where the films were extracted with water as the food simu¬ lant. In both Tables 4 and 5, the concentration of each extractable is in units of nanograms/milliliter. Zeolites can reduce the concentration of certain extractables which could cause regulatory issues.
TABLE 3

E3 = 2,2′-methylene bis (4-ethyl-6-( l-methylcyclohexyl)phenol).
TABLE 4

TABLE 5

In Table 6, two five-layer laminate structures in accordance with the invention, and one comparative four-layer laminate structure, are disclosed. The two five-layer structures were each made by laminating a coextruded four-layer film, using a conventional adhesive, to a second film (= layer 5). The comparative structure was made by laminating a coextruded three-layer film, using a conventional adhesive, to a second film (= layer 4).
TABLE 6

The target (and approximate actual) gauge (in mils) of each layer of the laminate structures of the invention was: layer 1 layer 2 layer 3 layer 4 adhesive layer 5
0.20 0.20 0.50 1.00 (minimal) 0.50
The target (and approximate actual) gauge (in mils) of each layer of the comparative laminate structures was:

The film of Examples 2 and 3 were subjected to food law migra¬ tion tests to evaluate whether zeolites could remove oxidation by¬ products. Their efficacy was compared with Comparative 2. The list of extractables can be found in Table 3. The test results from the extrac¬ tion of the films with Miglyol 812 (available from Hϋls America), a fatty food simulant, are summarized in Table 7. Zeolites can reduce the con¬ centration of certain extractables which could cause regulatory issues.
TABLE 7

D.L. = detection limit = 50 parts per billion (food equivalent). Q.L. = quantifiable limit = 150 parts per billion (food equivalent).
In Table 8, three five-layer laminate structures in accordance with the invention, and one comparative five-layer laminate structure, are disclosed. The five-layer structures were each made by laminating a coextruded four-layer film, using a conventional adhesive, to a second film (= layer 5).
TABLE 8

The target (and approximate actual) gauge (in mils) of each layer of the laminate structures of the invention and the comparative was:

Sliced turkey breast was stored in packages made from the films of Examples 4, 5, 6 and Comparative 3. A sensory panel tasted the turkey slices to evaluate whether or not zeolites can reduce the off- flavor caused by byproducts of the oxygen -scavenging reaction.
The films were triggered by ultraviolet light according to the pro¬ cedure disclosed in U.S. Patent No 5,21 1,875. The films were converted into packages on a Multivac© R7000 packaging machine. Cryovac T6070B film was used as the bottom web of the packages. Each pack¬ age contained one slice of turkey. Each package was flushed with a gas
SUBSTTI UTE SHEET (RULE 26)

Sliced turkey breast was stored in packages made from the films of Examples 7 and 8 and Comparatives 4 and 5. A sensory panel tasted the turkey slices to evaluate whether or not zeolites can reduce the off- flavor caused by the byproducts of the oxygen-scavenging reaction.
The films were triggered by ultraviolet light according to the pro¬ cedure disclosed in U.S. Patent No 5,211 ,875. The films were converted into packages on a Multivac® R7000 packaging machine. Cryovac® T6070B film was used as the bottom web of the packages. Each pack- age contained one slice of turkey. Each package was flushed with a gas mixture consisting of 99% N2 and 1% 02. Packages were stored in the dark for 7 days at 40°F.
A sensory panel rated the taste of the turkey slices. The scale ranged from 1 to 6, with 1 indicating extreme off-flavor and 6 indicating no off-flavor. Table 1 1 summarizes the percentage of the panelists which did not taste an off-flavor (i.e. a score of 6) in the packaged tur¬ key slices. In some cases, zeolites can significantly reduce the off-flavor caused by the byproducts of the oxygen-scavenging reaction.

A headspace gas chromatography (GC) method was used to de¬ termine the ability of a material to absorb aldehydes. The material

(either 6 to 7 mg of powder or 25mm disk of LLDPE film containing 4% absorber) was placed in a headspace GC vial (22 mL), and 2 μL of an al¬ dehyde mixture containing about 0.1% each of the indicated aldehydes in methanol was injected into each vial. The vials were incubated at 80 °C for 1 hour and were injected into a GC. The data in Table 12 shows the percent change in the aldehyde concentration for each material relative to an appropriate control (vial with no absorber or LLDPE disk) .
Table 12. Percent of Aldehydes Absorbed by Candidate Absorbers

n/t means not included in this test.
The data in Table 12 shows that various zeolites are capable of reducing the migration of aldehydes. In addition, due to specificity of various materials it can be seen that blends of materials can be advan- tageous.
Films of the invention can been made by any conventional means, including coextrusion, lamination, extrusion coating, or corona bond¬ ing, and then optionally irradiated and /or oriented. They can be made heat shrinkable through orientation or tenterframing if desired, at ori- entation ratios of 1:2 to 1:9 in either or both of the machine and trans¬ verse directions. For shrink applications, they can be made to have a free shrink of at least 10%, more preferably at least 20%, most pref¬ erably at least 30%, in either or both directions at 90°C.
Gasket compositions of the invention can be made by any con- ventional process, including, but not limited to, extrusion compounding for thermoplastic compositions, and conventional mixing equipment for plastisol compositions. The gasket compositions of the invention can

then be formed into gaskets on lids by any conventional process, in¬ cluding but not limited to, cold molding processes, inserted discs, ap¬ plication of liquid plastisols via pressurized nozzles followed by solidifi¬ cation in an oven, etc. Various changes and modifications may be made without depart¬ ing from the scope of the invention defined below. For example, a blend of different zeolites can be used in the same article (e.g. film or sealing compound). In films, although it is preferred that the zeolite be used in the film and as a packaging material such that the zeolite is disposed closer to the contents of the package, which can be food or any oxygen- sensitive product, than the oxygen scavenger, there may be applications where the zeolite is disposed “outside of the oxygen scavenger, such that the oxygen scavenger-containing layer is disposed closer to the contents of a package made from the film, than the zeolite -containing layer. The zeolite can alternatively be disposed on both sides of the oxygen scavenger. Also, within the same film, a first zeolite can be used in a first layer, and a second zeolite, different from the first zeolite, can be used in another layer of the film.
Alternatively, the zeolite, in addition to or instead of the arrange- ments described above, can be disposed in the same layer or layers as the oxygen scavenging material. Thus, by way of example, any of layers 14, 34, 44, and 54 of the examples and figures can include any suitable percent, by weight of the layer, of a zeolite. A preferred blend of oxygen scavenging and zeolite in such a blend layer is between 95% and 99.5% oxygen scavenger, and between 0.5% and 5% zeolite. Any suitable polymeric materials can be employed in films containing the zeolites, and are not limited to those listed herein.
The amount of zeolite used in a film of the present invention is preferably between 0.1 % and 5% of the layer in which it occurs. These percentages are based on the zeolite material (e.g. zeolite) per se, with suitable adjustment to be made if the zeolite material is used as a

masterbatch with another material such as polyethylene. Above 5% of the layer, optics of the film can be compromised to some extent, al¬ though the film can still be used in many applications. In end-use applications where optics are not a critical feature of the package, such as opaque films or gaskets for containers, higher amounts of zeolites can be beneficially used.
Zeolites disclosed herein can be used with or in films or coatings, or absorbed into a variety of other supports for scavenging or other uses, such as a layer or coating on another object, or as a bottle cap or bottle liner, as an adhesive or non-adhesive insert, sealant, gasket, fi¬ brous matte or other inserts, or as a non-integral component of a rigid, semi-rigid, or flexible container.

Claims (20)

WHAT IS CLAIMED IS:

1. An article of manufacture comprising an oxygen scavenger and a zeolite.

2. The article of claim 1 wherein the article comprises a film.

3. The film of claim 2 wherein the film comprises: a) a layer comprising an oxygen scavenger; and b) a layer comprising a zeolite.

4. The film of claim 2 wherein the film comprises a layer comprising an oxygen scavenger and a zeolite.

5. The film of claim 2 wherein the oxygen scavenger comprises a material selected from the group consisting of: i) oxidizable compound and a transition metal catalyst, ii) ethylenically unsaturated hydrocarbon and a transition metal catalyst, iii) ascorbate, iv) isoascorbate, v) sulfite, vi) ascorbate with a transition metal catalyst, the catalyst comprising a simple metal or salt, or a compound, complex or chelate of the transition metal; vii) a transition metal complex or chelate of a polycarboxylic acid, salicylic acid, or polyamine; viii) a reduced form of a quinone, a photoreducible dye, or a carbonyl compound which has absorbence in the UV spec- trum, and ix) tannin.

6. The film of claim 2 wherein the zeolite is selected from the group consisting of microporous crystalline aluminosilicates and micro- porous crystalline aluminophosphates.

7. The film of claim 2 wherein the zeolite comprises a synthetic zeo¬ lite.

8. The film of claim 2 further comprising an oxygen barrier layer.

9. The film of claim 2 further comprising an abuse resistant layer.

10. The film of claim 2 further comprising a heat sealable layer.

1 1. The film of claim 2 further comprising an intermediate adhesive layer disposed between any of the abuse-resistant layer and oxy¬ gen barrier layer, between the oxygen barrier layer and the layer comprising the oxygen scavenger, between the layer comprising the oxygen scavenger and the layer comprising the zeolite, and between the layer comprising the zeolite and the heat sealable layer.

12. The film of claim 2 wherein the film is cross-linked.

13. The film of claim 2 wherein the film is oriented.

14. The film of claim 2 wherein the film is heat shrinkable.

15. The article of claim 1 wherein the article is in the form of a seal- ing compound.

16. The sealing compound of claim 15 wherein the sealing compound is in the form of a gasket.

17. The gasket of claim 16 wherein the gasket comprises a polymer, an oxygen scavenger, and a zeolite.

18. The gasket of claim 16 wherein the gasket adheres a lid to a rigid or semi-rigid container.

19. A package comprising: a) an oxygen-sensitive article; and b) a container into which the oxygen sensitive article is dis- posed, the container including a component comprising an oxygen scavenger, and a zeolite.

20. A method of making an article of manufacture having reduced migration of by-products of an oxygen scavenging reaction comprising providing an article comprising an oxygen scavenger and a zeolite; and exposing the article to actinic radiation.

AU19886/97A
1996-03-07
1997-03-07
Zeolite in packaging film

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(en)

1996-03-07
1997-03-07
Zeolite in packaging film

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(en)

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Cited By (1)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

AU741535B2
(en)

1997-05-16
2001-12-06
Cryovac, Inc.
Amorphous silica in packaging film

Families Citing this family (39)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

US5904960A
(en)

1997-10-29
1999-05-18
Cryovac, Inc.
Method and apparatus for treating an article containing an oxidizable organic compound

JP3824036B2
(en)

1998-02-18
2006-09-20
三菱瓦斯化学株式会社

Oxygen absorber composition

SE515824C2
(en)

2000-01-26
2001-10-15
Tetra Laval Holdings & Finance

Method for manufacturing a multilayered packaging laminate by wet coating, as well as laminates made according to the procedure

DE10020621A1
(en)

2000-04-27
2001-11-08
Degussa

Colorless, low-emission polymer

US6525123B1
(en)

2000-05-19
2003-02-25
Chevron Phillips Chemical Company Lp
Compatible blend systems from ethylene vinyl alcohol and oxygen scavenging polymers

JP4823411B2
(en)

2000-09-01
2011-11-24
株式会社クラレ

Oxygen-absorbing resin composition

US7740926B2
(en)

2001-07-26
2010-06-22
M&G Usa Corporation
Oxygen-scavenging containers

US6780916B2
(en)

2001-07-26
2004-08-24
M & G Usa Corporation
Oxygen-scavenging resin compositions having low haze

JP4656367B2
(en)

2003-07-18
2011-03-23
東洋製罐株式会社

Oxygen-absorbing material, oxygen-absorbing resin composition, and oxygen-absorbing laminate

US20050085577A1
(en)

2003-09-11
2005-04-21
Ta Yen Ching
Oxygen scavenging packaging having improved sensory properties

US20050129812A1
(en)

2003-12-12
2005-06-16
Brown Martha J.M.
Packaging for eliminating off-odors

EP1721737B1
(en)

2004-02-19
2016-11-09
Toyo Seikan Kaisha, Ltd.
Plastic multilayer structure

JP5024718B2
(en)

2004-06-18
2012-09-12
東洋製罐株式会社

Odor trapping resin composition

US7241481B2
(en)

2004-06-25
2007-07-10
Cryovac, Inc.
Method of removing sulfur odors from packages

US7332025B2
(en)

2004-08-24
2008-02-19
The Nippon Synthetic Chemical Industry Co., Ltd.
Resin composition and process for preparing multi-layer structure using the same

US7371335B2
(en)

2004-10-21
2008-05-13
E.I. Dupont De Nemours And Company
Curable thick film compositions for use in moisture control

US7514152B2
(en)

2005-02-10
2009-04-07
Cryovac, Inc.
Oxygen scavenging film with good interply adhesion

US7691290B2
(en)

2005-02-15
2010-04-06
Constar International Inc.
Oxygen scavenging compositions and packaging comprising said compositions

TWI292340B
(en)

2005-07-13
2008-01-11
Ind Tech Res Inst
Antireflective transparent zeolite hardcoat film, method for fabricating the same, and solution capable of forming said transparent zeolite film

US7629009B2
(en)

2005-11-28
2009-12-08
G3 Enterprises
Highly selective molecular confinement for the prevention and removal of taint in foods and beverages

US20080063845A1
(en)

2006-09-12
2008-03-13
Excel-Pac Inc.
Multilayer structures, uses and preparation thereof

WO2009020688A1
(en)

2007-05-21
2009-02-12
University Of Maine System Board Of Trustees
Zeolite composite materials for waste odor control

US20090045095A1
(en)

2007-08-13
2009-02-19
Bag Innovations Group, Llc
Packaging for Extending Life of Respiring Produce and Other Perishable Foodstuffs

AU2008340129B2
(en)

2007-12-21
2013-10-17
Basf Se
Oxygen-scavenging mixtures

US20100237068A1
(en)

2009-03-17
2010-09-23
Rubbermaid Incorporated
Container With In-Molded Exposed Panel

CN102712865B
(en)

2009-11-30
2016-06-08
路博润公司
Stabilized mixture containing friction improver

CO6380009A1
(en)

2010-08-13
2012-02-15
Perilla Jorge Alberto Medina

OXYGEN ABSORBING COMPOUND ENCAPSULATED IN A SILICA MATRIX AND METHOD TO PRODUCE IT

TWI515113B
(en)

2010-09-01
2016-01-01
Kyodo Printing Co Ltd

Laminated body, packaging container and package

DE202011104629U1
(en)

2011-06-24
2011-11-16
Smurfit Kappa Hoya Papier Und Karton Gmbh

Fiber product for packaging

CA2871480C
(en)

2012-04-30
2021-08-17
Plastipak Packaging, Inc.
Oxygen scavenging compositions

JP5582181B2
(en)

2012-09-28
2014-09-03
東洋製罐株式会社

Multi-layer container

US9415990B2
(en)

2013-02-13
2016-08-16
Cryovac, Inc.
Bag-in-box system for use in dispensing a pumpable product

WO2015102614A1
(en)

2013-12-31
2015-07-09
Multisorb Technologies, Inc.
Oxygen scavenging film containing moisture regulator

US11338983B2
(en)

2014-08-22
2022-05-24
Plastipak Packaging, Inc.
Oxygen scavenging compositions, articles containing same, and methods of their use

US10351692B2
(en)

2014-10-17
2019-07-16
Plastipak Packaging, Inc.
Oxygen scavengers, compositions comprising the scavengers, and articles made from the compositions

JP2016193731A
(en)

2015-03-31
2016-11-17
株式会社吉野工業所
Humidity conditioning container

MX2017015176A
(en)

2015-05-29
2018-04-13
Cryovac Inc
Oxygen scavenging films.

AR108339A1
(en)

2016-04-27
2018-08-08
Cryovac Inc

MOVIE THAT HAS AN OXYGEN CLEANER AND A VOLATILE ORGANOLEPTIC COMPOUND CLEANER

KR20200062251A
(en)

2017-09-29
2020-06-03
다이니폰 인사츠 가부시키가이샤

Sealant film for packaging liquid contents and a laminate comprising the same, and packaging material for liquid contents, package for liquid contents

Family Cites Families (60)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

US3977901A
(en)

1974-10-23
1976-08-31
Westinghouse Electric Corporation
Metal/air cells and improved air electrodes for use therein

US4230595A
(en)

1978-03-13
1980-10-28
Teijin Limited
Oxygen scavenging and heat-generating compositions, and deoxygenating and heat-generating structures

DE2833675C2
(en)

1978-08-01
1982-06-24
Degussa Ag, 6000 Frankfurt

Thermoplastic mixtures for the production of plastic films with antiblocking properties

US4366179A
(en)

1980-03-17
1982-12-28
Mitsubishi Gas Chemical Company, Inc.
Oxygen and carbon dioxide absorbent and process for storing coffee by using the same

US4536409A
(en)

1981-01-23
1985-08-20
American Can Company
Oxygen scavenger

US4540727A
(en)

1982-10-29
1985-09-10
Raychem Corporation
Polyamide compositions

JPS60163911A
(en)

1984-02-02
1985-08-26
Suriibondo:Kk
Photocurable rubbery elastic composition

JPS60223867A
(en)

1984-04-19
1985-11-08
Dainippon Toryo Co Ltd
Curable coating composition

KR890002855B1
(en)

1985-06-26
1989-08-05
미쯔비시 가스 가가구 가부시기가이샤
Sheet-type deoxide material

KR900001379B1
(en)

1985-09-13
1990-03-09
이데미쯔세끼유가가꾸 가부시기가이샤
Polyethylene resin composition

EP0223245A3
(en)

1985-11-21
1989-05-10
Mitsui Petrochemical Industries, Ltd.
Curable compositions for dental drugs having sustained release property

DE3804488A1
(en)

1987-02-14
1988-08-25
Mitsubishi Gas Chemical Co

OXYGEN ABSORPTION AGENT

JPH0618899B2
(en)

1987-06-30
1994-03-16
品川燃料株式会社

Film containing antibacterial zeolite

WO1989001012A1
(en)

1987-07-27
1989-02-09
Mb Group Plc
Improvements in and relating to packaging

US5227411A
(en)

1988-02-10
1993-07-13
W. R. Grace & Co.-Conn.
Sealed containers and sealing compositions for them

GB8803062D0
(en)

1988-02-10
1988-03-09
Grace W R & Co
Sealed containers & sealing compositions for them

US5204389A
(en)

1988-02-10
1993-04-20
W. R. Grace & Co.-Conn.
Sealed containers and sealing compositions for them

EP0367835B1
(en)

1988-04-30
1996-07-31
Toyo Seikan Kaisha, Ltd.
Multilayered plastic container

US5126174A
(en)

1989-02-16
1992-06-30
Wm. Wrigley Jr. Company
Food packaging improvements

JPH0649354B2
(en)

1989-07-10
1994-06-29
東洋製罐株式会社

Plastic multi-layer container

JPH02269667A
(en)

1990-03-26
1990-11-05
Toyo Seikan Kaisha Ltd
Container lid

DK0527207T3
(en)

1990-05-02
2001-02-26
Grace W R & Co

Polymer composition containing oxygen scavenging compounds

ES2144461T3
(en)

1990-05-02
2000-06-16
Grace W R & Co

POLYMER COMPOSITIONS CONTAINING OXYGEN SENSING COMPOUNDS.

JPH0474515A
(en)

1990-07-13
1992-03-09
Toray Ind Inc
Oxygen absorbing body

ZA924298B
(en)

1991-03-14
1993-04-28
Nat Brands Limited
Oxygen scavenger system

CA2062083C
(en)

1991-04-02
2002-03-26
Drew Ve Speer
Compositions, articles and methods for scavenging oxygen

US5364555A
(en)

1991-04-30
1994-11-15
Advanced Oxygen Technologies, Inc.
Polymer compositions containing salicylic acid chelates as oxygen scavengers

US5211875A
(en)

1991-06-27
1993-05-18
W. R. Grace & Co.-Conn.
Methods and compositions for oxygen scavenging

JPH05247276A
(en)

1992-03-04
1993-09-24
Toppan Printing Co Ltd
Oxygen-barrier resin composition

JPH05319411A
(en)

1992-05-21
1993-12-03
Dainippon Ink & Chem Inc
Packaging method and packaging material

US5492741A
(en)

1992-06-19
1996-02-20
Fuji Photo Film Co., Ltd.
Packaging material for photographic photosensitive materials and light-shielding bag formed thereof

BR9202713A
(en)

1992-07-13
1994-02-01
Itap S A

A PVC-FREE ELASTOMERIC THERMOPLASTIC COMPOSITION INTENDED TO MAKE SELLERS FOR DRINK CONTAINER LID

HU9202502D0
(en)

1992-07-31
1992-10-28
Laszlo Toth
Plastic-based packaging material of absorbent effect and method for producing said material

JPH06100042A
(en)

1992-09-14
1994-04-12
Toppan Printing Co Ltd
Oxygen barrier laminate

US5310497A
(en)

1992-10-01
1994-05-10
W. R. Grace & Co.-Conn.
Oxygen scavenging compositions for low temperature use

US5284892A
(en)

1992-11-10
1994-02-08
E. I. Du Pont De Nemours And Company
Aldehyde scavenging compositions and methods relating thereto

CN1096315A
(en)

1992-11-24
1994-12-14
联邦科学及工业研究组织
Deoxidizing compositions

JPH06183453A
(en)

1992-12-17
1994-07-05
Toyo Seikan Kaisha Ltd
Container lid

JPH06263172A
(en)

1993-03-12
1994-09-20
Toppan Printing Co Ltd
Deodorant, oxygen-barriering laminated body

US5362784A
(en)

1993-05-28
1994-11-08
E. I. Du Pont De Nemours And Company
Aldehyde scavenging compositions and methods relating thereto

DK0659195T4
(en)

1993-07-13
2002-08-26
Chevron Chem Co

Ethylene-containing oxygen scavenging compositions and processes for preparing them by esterification or transesterification in a reaction extruder

US5744056A
(en)

1993-07-16
1998-04-28
Amoco Corporation
Oxygen-scavenging compositions and articles

JP2699814B2
(en)

1993-08-06
1998-01-19
東洋製罐株式会社

Plastic multilayer container and cooked rice package with excellent flavor retention

JP3630706B2
(en)

1993-09-01
2005-03-23
東洋製罐株式会社

Plastic multilayer container with excellent content preservation

AU1305195A
(en)

1993-12-14
1995-07-03
Zapata Technologies, Inc.
Liner composition for a closure element for a fluid container

US5413827A
(en)

1994-01-03
1995-05-09
E. I. Du Pont De Nemours And Company
Aldehyde scavenging compositions and methods relating thereto

EP0664317A1
(en)

1994-01-19
1995-07-26
Du Pont De Nemours International S.A.
Deodorized thermoplastics

JPH07227260A
(en)

1994-02-14
1995-08-29
Sumitomo Chem Co Ltd
Multilayer sheet for oxygen absorption

JPH07227940A
(en)

1994-02-16
1995-08-29
Goyo Paper Working Co Ltd
Sheet base material for food container

DE4424775A1
(en)

1994-07-05
1996-01-11
Grace Gmbh

Antiblocking agent and process for its manufacture

JPH10504341A
(en)

1994-08-15
1998-04-28
チバスペシャルティケミカルズホールディングインコーポレーテッド

Stabilized PVC containing PVC

JPH08132573A
(en)

1994-11-07
1996-05-28
Toppan Printing Co Ltd
Oxygen absorbing laminate

WO1996022160A1
(en)

1995-01-17
1996-07-25
E.I. Du Pont De Nemours And Company
Sulfide scavenging packaging materials

JPH0929901A
(en)

1995-05-17
1997-02-04
Nippon Tetrapack Kk
Laminate for packing liquid food

CA2223867A1
(en)

1995-06-07
1996-12-19
E.I. Du Pont De Nemours And Company
Sulfide scavenging packaging materials

WO1997000905A1
(en)

1995-06-20
1997-01-09
Ciba Specialty Chemicals Holding Inc.
Stabilized polyvinyl chloride containing recycled material

US5798055A
(en)

1995-12-15
1998-08-25
Blinka; Thomas Andrew
Oxygen scavenging metal-loaded ion-exchange compositions

EP0868400A4
(en)

1995-12-15
1999-03-17
Grace W R & Co
Oxygen scavenging metal-loaded ion-exchange compositions

ATE204595T1
(en)

1996-03-07
2001-09-15
Cryovac Inc

ZEOLITE IN A PACKAGING FILM

US5942297A
(en)

1996-03-07
1999-08-24
Cryovac, Inc.
By-product absorbers for oxygen scavenging systems

1997

1997-03-07
CN
CNB01141135XA
patent/CN1235956C/en
not_active
Expired – Fee Related

1997-03-07
CN
CN97194442A
patent/CN1090201C/en
not_active
Expired – Fee Related

1997-03-07
JP
JP53194397A
patent/JP3529139B2/en
not_active
Expired – Lifetime

1997-03-07
EP
EP19970908040
patent/EP0885257B1/en
not_active
Expired – Lifetime

1997-03-07
WO
PCT/US1997/003526
patent/WO1997032924A1/en
active
IP Right Grant

1997-03-07
NZ
NZ331414A
patent/NZ331414A/en
not_active
IP Right Cessation

1997-03-07
CA
CA 2247904
patent/CA2247904C/en
not_active
Expired – Fee Related

1997-03-07
DK
DK97908040T
patent/DK0885257T3/en
active

1997-03-07
AU
AU19886/97A
patent/AU727948C/en
not_active
Expired

1997-03-07
BR
BR9708172A
patent/BR9708172A/en
not_active
IP Right Cessation

1998

1998-05-07
US
US09/074,058
patent/US6365245B2/en
not_active
Expired – Lifetime

2000

2000-10-18
US
US09/691,570
patent/US6391403B1/en
not_active
Expired – Fee Related

2001

2001-07-31
US
US09/919,225
patent/US6458438B2/en
not_active
Expired – Lifetime

Cited By (2)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

AU741535B2
(en)

1997-05-16
2001-12-06
Cryovac, Inc.
Amorphous silica in packaging film

AU741535C
(en)

1997-05-16
2005-07-21
Cryovac, Inc.
Amorphous silica in packaging film

Also Published As

Publication number
Publication date

US20020018865A1
(en)

2002-02-14

US20010008662A1
(en)

2001-07-19

US6391403B1
(en)

2002-05-21

AU727948B2
(en)

2001-01-04

EP0885257B1
(en)

2001-08-22

CN1235956C
(en)

2006-01-11

JP3529139B2
(en)

2004-05-24

WO1997032924A1
(en)

1997-09-12

CN1218488A
(en)

1999-06-02

AU727948C
(en)

2005-10-27

JP2002504159A
(en)

2002-02-05

EP0885257A1
(en)

1998-12-23

DK0885257T3
(en)

2001-10-08

CN1090201C
(en)

2002-09-04

BR9708172A
(en)

1999-07-27

NZ331414A
(en)

2000-04-28

US6365245B2
(en)

2002-04-02

CA2247904C
(en)

2002-09-03

CA2247904A1
(en)

1997-09-12

CN1394902A
(en)

2003-02-05

US6458438B2
(en)

2002-10-01

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