US20020001684A1 - Barrier compositions and articles made therefrom - Google Patents
Barrier compositions and articles made therefrom Download PDFInfo
- Publication number
- US20020001684A1 US20020001684A1 US08/941,873 US94187397A US2002001684A1 US 20020001684 A1 US20020001684 A1 US 20020001684A1 US 94187397 A US94187397 A US 94187397A US 2002001684 A1 US2002001684 A1 US 2002001684A1
- Authority
- US
- United States
- Prior art keywords
- mxd6
- blend
- ppm
- polyester
- multiple layer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 118
- 230000004888 barrier function Effects 0.000 title claims abstract description 94
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 83
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 83
- 239000001301 oxygen Substances 0.000 claims abstract description 83
- 239000010410 layer Substances 0.000 claims abstract description 73
- 229920000728 polyester Polymers 0.000 claims abstract description 56
- 239000004952 Polyamide Substances 0.000 claims abstract description 40
- 229920002647 polyamide Polymers 0.000 claims abstract description 40
- MMEDJBFVJUFIDD-UHFFFAOYSA-N 2-[2-(carboxymethyl)phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC=C1CC(O)=O MMEDJBFVJUFIDD-UHFFFAOYSA-N 0.000 claims abstract description 37
- 239000010941 cobalt Substances 0.000 claims abstract description 27
- 229910017052 cobalt Inorganic materials 0.000 claims abstract description 27
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims abstract description 26
- 125000006839 xylylene group Chemical group 0.000 claims abstract description 24
- 239000012792 core layer Substances 0.000 claims abstract description 14
- 229920006121 Polyxylylene adipamide Polymers 0.000 claims description 108
- 101000576320 Homo sapiens Max-binding protein MNT Proteins 0.000 claims description 107
- 229920002292 Nylon 6 Polymers 0.000 claims description 39
- 239000004677 Nylon Substances 0.000 claims description 36
- 238000000034 method Methods 0.000 claims description 36
- 229920001778 nylon Polymers 0.000 claims description 36
- 239000003054 catalyst Substances 0.000 claims description 32
- 229910052723 transition metal Inorganic materials 0.000 claims description 15
- 150000003624 transition metals Chemical class 0.000 claims description 15
- 238000004806 packaging method and process Methods 0.000 claims description 13
- 238000010101 extrusion blow moulding Methods 0.000 claims description 7
- 235000013305 food Nutrition 0.000 claims description 7
- 238000002156 mixing Methods 0.000 claims description 5
- 239000011241 protective layer Substances 0.000 claims description 5
- 239000000565 sealant Substances 0.000 claims description 5
- 238000000071 blow moulding Methods 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 229920000098 polyolefin Polymers 0.000 claims description 3
- 239000012790 adhesive layer Substances 0.000 claims description 2
- 238000009459 flexible packaging Methods 0.000 claims 12
- 238000010438 heat treatment Methods 0.000 claims 3
- 239000002356 single layer Substances 0.000 abstract description 7
- 229920000139 polyethylene terephthalate Polymers 0.000 description 55
- 239000005020 polyethylene terephthalate Substances 0.000 description 55
- 239000000463 material Substances 0.000 description 38
- 238000010521 absorption reaction Methods 0.000 description 12
- 230000008569 process Effects 0.000 description 11
- 229920000232 polyglycine polymer Polymers 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 8
- 230000008859 change Effects 0.000 description 7
- 239000007789 gas Substances 0.000 description 7
- 238000001125 extrusion Methods 0.000 description 6
- -1 polyethylene Polymers 0.000 description 6
- 230000001954 sterilising effect Effects 0.000 description 6
- 229920006122 polyamide resin Polymers 0.000 description 5
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 150000001868 cobalt Chemical class 0.000 description 4
- UFRKOOWSQGXVKV-UHFFFAOYSA-N ethene;ethenol Chemical compound C=C.OC=C UFRKOOWSQGXVKV-UHFFFAOYSA-N 0.000 description 4
- 239000004715 ethylene vinyl alcohol Substances 0.000 description 4
- 230000000670 limiting effect Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 241001312297 Selar Species 0.000 description 3
- 229920003365 Selar® Polymers 0.000 description 3
- 230000002939 deleterious effect Effects 0.000 description 3
- 239000005022 packaging material Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 230000002000 scavenging effect Effects 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 208000035155 Mitochondrial DNA-associated Leigh syndrome Diseases 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 235000013405 beer Nutrition 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 208000003531 maternally-inherited Leigh syndrome Diseases 0.000 description 2
- 235000013372 meat Nutrition 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 229920013683 Celanese Polymers 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 229940123973 Oxygen scavenger Drugs 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 229920001986 Vinylidene chloride-vinyl chloride copolymer Polymers 0.000 description 1
- FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 238000004299 exfoliation Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 235000014214 soft drink Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
Images
Classifications
-
- 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
- C08K3/02—Elements
- C08K3/08—Metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
-
- 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.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
-
- 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
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31562—Next to polyamide [nylon, etc.]
-
- 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
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31565—Next to polyester [polyethylene terephthalate, etc.]
-
- 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
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31725—Of polyamide
- Y10T428/31736—Next to polyester
-
- 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
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31786—Of polyester [e.g., alkyd, etc.]
Definitions
- a problem with conventional barrier materials is that due to their high cost or their unstable structural characteristics or other weaknesses, it is difficult to fabricate commercial packaging solely out of barrier materials.
- EVOH while having superior oxygen barrier properties, suffers moisture problems because of the many hydroxyl groups in the polymer.
- Other barrier materials are so expensive that to manufacture structures solely from those barriers would be cost prohibitive. Accordingly, it has become a common practice to use multilayer structures, whereby, the amount of expensive or sensitive barrier material may be reduced to a thin layer and an inexpensive polymer can be used on one or both sides of the barrier layer as structural layers.
- the use of multilayer structures permits the barrier layer to be protected from Deterioration by structural layers on one or both sides of the barrier layer.
- multilayer structures containing a barrier layer may be cheaper and stronger than a single layer of barrier materials, such structures are more complicated to Manufacture than single-layered ones.
- multilayer structures comprised of layers of a variety of different materials may be opposed in some instances on environmental grounds, they may be more difficult to recycle since it is often difficult and expensive to separate the layers.
- reducing the thickness of the barrier layer in a multilayer structure can reduce the barrier properties of the film. Accordingly, there is a need for a single-layer packaging material with suitable barrier properties but without the cost or structural weaknesses of packaging made solely from a barrier material.
- additional multilayer structures having improved barrier properties wherein, the barrier material is reduced to a thinner layer and replace in part by inexpensive structural layers. These structures have the same barrier properties of prior art barriers but at lower cost due to a decrease in the amount of expensive barrier material used.
- oxygen absorption or oxygen scavenging materials are useful in reducing the amount of oxygen that contaminate the product packaged in the container.
- An example of oxygen scavenging materials and methods of using them is disclosed in U.S. Pat. No. 4,425,410 to Farrell et al, the disclosure of which is hereby incorporated by reference herein.
- Another useful aspect of oxygen absorbing material is that such materials can reduce residual oxygen which is trapped in the headspace of a container during sealing, thereby preventing it from having a deleterious effect on the packaged products.
- PET polyethylene terephthalate resin
- PEN polyethylene naphthalate
- polyesters In order to enhance polyester's gas barrier properties, polyesters have been used in a multilayer structure in combination with a layer having excellent gas barrier properties such as EVOH.
- a layer having excellent gas barrier properties such as EVOH.
- multilayer structures employing polyester, such as PET Frequently have adhesion problems between the polyester and the barrier layer which frequently leads to delamination over time.
- One approach to enhancing the gas barrier property of PET is to use a resin mixture which includes PET and a xylylene group containing polyamide resin.
- resin materials are disclosed in U.S. Pat. No. 4,501,781 to Kushida en al.
- One of the considerations encountered with such blends accordingly to Kushida is that there is a limit to the amount of xylylene group-containing polyamide resin that may be present in the PET blend.
- Kushida indicates that amounts of xylylene group-containing polyamide resin greater than 30% by weight causes the container to become a laminated foil structure which is susceptible to exfoliation between the foil layers of the container.
- the permeation of oxygen gas through the walls of a container is less when the container is made with PET and a xylylene group-containing polyamide than when the container is made solely of PET.
- Kushida reports that a bottle shaped container made with PET-xylylene group-containing polyamide measured 0.0001 cc of oxygen Permeation per day compared to 0.0180 cc of oxygen permeation per day for a container made with PET.
- a preferred xylylene group-containing polyamide resin in the present invention is an aromatic polyamide formed by polymerizing meta-xylylene-diamine (H 2 NCH 2 —m—C 6 H 4 —CH 2 NH 2 ) with adipic acid (HO 2 C(CH 2 ) 4 CO 2 H) .
- the most preferred such polymer is manufactured and sold by Mitsubishi Gas Chemicals, Japan, under the designation MXD6 or MXD6 nylon.
- the gas barrier property of polyester is enhanced by blending polyester with xylylene group-containing polyamide and a transition metal catalyst.
- Preferred embodiments include blends of PET/MXD6/Cobalt and exhibit superior oxygen barrier and oxygen absorption characteristics that were not present in the prior art structures.
- the structures in this invent-on are not as clear as the prior art structures.
- Hong discloses that it is believed that the high orientation of the blend increases the surface areas and interface between PET and MXD6 nylon so that there are a greater number of sites at which a reaction or an absorption of oxygen catalyzed by the transition metal catalyst takes place. This increased surface area and interface between PET and MXD6 nylon also causes a change in the refractive characteristics of the materials and results in an increased diffusion of light passing through the structures.
- the disclosures made in the Hong application are hereby incorporated by reference herein.
- FIG. 1 shows a pouch, sealed on three sides and made with the sheet structure of this invention.
- FIG. 2 shows a cross-section of the pouch of FIG. 1 taken at 2 - 2 of FIG. 1.
- FIG. 3 shows a cross-section of sheet structure used to form the pouch shown in FIGS. 1 and 2.
- MXD6 nylon oxygen barrier properties of MXD6 nylon are improved by the addition of cobalt octoate and that structures formed from MXD6/cobalt octoate blends and MXD6/cobalt octoate/PET blends have improved clarity and retort characteristics.
- the blends can be made into structures in the form of containers, films, sheets, pouches or lidstock.
- he MXD6/cobalt salt blend and the MXD6/cobalt salt/PET blend can be a single layer film or one layer of a multiple layer film which has been coextruded, extrusion coated or laminated.
- PET is the preferred polyester used in the MXD6/cobalt octoate/polyster blends
- any thermoformable grade polyester with oxygen barrier qualities greater than those of polyolefins can be used.
- PET blends is utilized to produce clear structures having improved oxygen barrier properties by limiting the degree of orientation so that the MXD6 domain increases in size up to less than the wavelength of light.
- the oxygen barrier and oxygen absorbing compositions of the present invention can also be formed into multiple Layer structures. These multiple layer structures have a core layer of either a MXD6 nylon/cobalt octoate blend or a MXD6 nylon/polyester/cobalt octoate blend disposed between two adjacent layers.
- the two adjacent layers are comprised of either a Polyester or a polyamide.
- one adjacent layer can be a polyester and the other adjacent layer can be a polyamide.
- the polyester is PET and the polyamide is nylon 6.
- these structures are orientated to a degree so that the MXD6 domain increases in size up to less than the wavelength of light.
- any thermoformable grade polyester with oxygen barrier qualities greater than those of polyolefins can be used to form clear packages and containers with almost zero oxygen permeability when blended with MXD6 and cobalt octzate. It has been discovered that the problem of haze is solved by extrusion blow molding the blend when it is in a molten state. This minimizes the orientation that occurs when the packages or containers are fabricated. By limiting the orientation, the domain sizes of the polyester and MXD6 do not increase to where they are greater than the wavelength of light and diffusion occurs.
- Table 2 shows a comparison of the amount of haze in bottles produced by extrusion blow molding and injection-reheat blow molding.
- the extrusion blow molded bottles display a significant reduction in the percent haze.
- TABLE 2 COMPARISON OF THE HAZE OF INJECTION BLOW MOLDED AND EXTRUSION BLOW MOLDED BOTTLES NORMALIZED HAZE BOTTLES (% HAZE/MIL) INJECTION-REHEAT 3.16 BLOW MOLDED EXTRUSION BLOW 0.2 MOLDED-MATTE FINISH MOLD EXTRUSION BLOW 0.12 MOLDED-POLISHED MOLD
- Cast film were prepared using Selar polyester which was blended with MXD6 nylon with and without the addition of cobalt octoate. In the presence of MXD6, these films showed a mild grey color. However, when these films were thermoformed, clear structures were produced. Moreover, haze was significantly reduced by minimizing the degree of orientation. Table 3 shows the normalized % haze/mil of materials compared to haze in injection-reheat blow molded bottles.
- the composition of the present invention also comprises a blend of polyester, such a PET, and up to about 30% of a barrier material, such as a xylylene group-containing polyamide with about 49 ppm to about 110 ppm catalyst, most preferably in the form of a nascent catalyst residue from the PET.
- the barrier material is preferably a xylylene group-containing polyamide rein commonly known as MXD6 nylon which is available from Toyobo or Mitsubishi Gas Chemicals Company.
- the PET is available from Eastman Hoechst Celanese, ICI America, Shell Chemical or DuPont.
- the catalyst is a transition metal. Cobalt has been found to be Particularly useful in the present invention. Transition metal catalysts are defined as catalysts of metals which have filled or partially filled outer “d” orbitals or are those having filled “d” orbitals and filled or partially filled “p” orbitals.
- Multi-layer structures having a barrier layer of MXD6 nylon and two outer layers of PET wherein the MXD6 nylon comprises about 10 wt. % of the total structure will provide a clear film or ccrtainer.
- the oxygen barrier properties of such multilayer structures are not as good as blends of the present invention.
- such multiayer structures will not provide the oxygen absorption capabilities of the present invention.
- a physical blend of the pellets be made in a suitable mixing device.
- the process disperses the particles of he barrier material in the polyester.
- PET, MXD6 nylon and cobalt salt are mixed together in a screw extruder to form a blend. This extrusion is then oriented to a limited degree by extrusion blow-molding to form a structure such as a container or bottle.
- the barrier material is normally present as spherical particles dispersed in PET.
- Containers made in accordance with this method are clear, unlike the prior art structures described above. However, these containers exhibit the same superior oxygen barrier and oxygen absorption characteristics of the prior art structures disclosed by Hong.
- a blend consisting of PET, up to about 30 wt. % MXD6 nylon (preferably up to 10 wt. % MXD6 nylon) and up to about 110 ppm cobalt salt is coextruded as a barrier Layer with a layer of PET on each surface thereof to form a three layer structure.
- the barrier layer would be a blend of 10 wt. % MXD6 nylon and the overall percentage of MXD6 nylon in the structure would be about 2 wt. %.
- Containers made from this structure are clear and do not exhibit the haze found in prior art containers.
- the catalyst in the blends of the present invention improves the barrier properties of structures made therefrom by providing oxygen absorption capabilities.
- compositions of blends of a xylylene group—containing polyamide and up to 250 PPM of a transition metal catalyst do not have heir oxygen barrier characteristics adversely affected by the high relative humidity conditions experienced during retort. Therefore, they can be used to form films that do not require additional moisture barrier layers.
- the preferred blends of these compositions are comprised of MXD6 and cobalt octoate and they are used to form the oxygen barrier layer of a single or multiple layer film.
- the barrier layer is disposed between two adjacent layers.
- One, or both, of the adjacent layers is comprised of a polyester or a polyamide.
- the preferred polyester As PET and the preferred polyamide is nylon 6.
- these compositions are oriented to a degree so that the MXD6 domain increases in size up to less than the wavelength of light.
- FIG. 1 illustrates a pouch such as is the desired packaging structure of one of the embodiments of this invention.
- a cross-section of a portion of the pouch is shown in FIG. 2.
- the sheet material used to make the pouch is seen in FIG. 3.
- the FIG. 2 construction consists of two sheet elements of the FIG. 3 construction in face to face relation with the layers 12 joined at the one edge in heat seal.
- the pouch is formed by arranging the two sheet elements in face to face relationship and forming heat seals 19 about the common periphery.
- the pouch may be formed by folding a sheet element onto itself and forming heat seals about the edges. Either way the formed pouch appears as shown in FIG. 1.
- layer 12 is a heat sealable layer comprised of a polyester or a polyamide.
- Layer 14 is an optional adhesive, or tie layer, selected based on the materials in the adjacent layers.
- Layer 16 a blend of a xylylene group-containing polyamide and up to 250 ppm of a transition metal catalyst.
- Layer 18 is also an optional adhesive, or tie, layer and is also selected based on the materials in the adjacent layers.
- Layer 20 is an outer protective layer comprised of a polyester or a polyamide.
- the formed pouch is intended for packaging products which are subjected to a sterilizing process after the product is in the package and the package is sealed.
- a common sterilizing process is known as autoclave, or retort, processing.
- closed and sealed packages are placed in a pressure vessel. Steam and water are then introduced into the vessel at about 275° F. at a sufficiently high pressure to permit maintenance of the desired temperature. The temperature and pressure are usually maintained for about 30 minutes. Finally, the pressure vessel is cooled and the pressure temporarily maintained until the packages cool Internally. Finally the pressure is released and the processed packages are removed.
- Sheet structures of this invention generally range in thickness from about 3 mils up to about 10 mils.
- the thickest layer is usually the sealant layer and the thinnest layers usually are the tie layers and the oxygen barrier layer.
- the sheet structures of this invention may be made by conventional processes and combinations of processes.
- the process and its sequences may be selected according to the equipment and polymers available.
- the specific structure selected and the compositions of the oxygen barrier layer and the outer layers of polyester will be at least partially dependent on the process and its sequences.
- concentrations of about 49 ppm to about 120 ppm residual catalyst in a polyester-barrier material blend such as a PET-xylylene group-containing polyamide resin blend, have not only superior oxygen barrier properties but also significant oxygen scavenging capabilities.
- compositions having superior oxygen barrier and oxygen absorption characteristics may be employed as a mono or multilayer film, such as, for example, in a pouch or flexible lidstock. These compositions may also be formed into rigid containers or may comprise the sidewall, body, lid or entire container. Also, the composition of the present invention may be formed into a chip and used in a container as an oxygen scavenger.
- a preferred embodiment of the present invention is a bend of PET and MXD6 nylon, wherein the MXD6 nylon is present in an amount of from about 2.5 weight % to about 15 weight % with the balance being PET. Cobalt is present in a range of 49 ppm to about 120 ppm with 62 ppm being most preferable.
- Another embodiment is pure MXD6 with between 49 and 120 ppm cobalt.
- the MXD6 nylon is present in an amount of from about 4 weight % to about 10 weight % with the balance being PET.
- Cobalt is preferably present in the range of from about 49 ppm to about 120 ppm and most preferably present in an amount of about 62 ppm.
- MXD6 nylon is present In the blend in an amount of about 7.5% with the remainder being PET and cobalt, present in the amounts stated above.
- nascent cobalt is present as a residual of the PET polymerization catalyst.
- Specially added cobalt is preferably present as a cobalt salt dispersed in mineral spirits such as that sold under the trademark Nuodex by Huls America.
- the Nuodex products contain up to about 15% by weight cobalt.
- the preferred maximum amount of catalyst is about 250 ppm and is dependent on the structure being formed from the PET/MXD6/cobalt blends.
- the xylylene group containing polyamide is preferably a MXD6 nylon which is produced by condensation polymerization of metha-xylylene diamine (MXDA) and adipic acid.
- MXDA metha-xylylene diamine
- the degree of orientation not exceed the limit at which the refractive characteristics of the blend materials change and the clarity of the structures deteriorates.
- the multiple layer sheet structures have outer layers comprised of polyesters or polyamides that are suitable for heat sealing.
- an adhesive layer is disposed on one or both sides of the barrier blend layer to bond the polyester or polyamide layers to the blend layer.
- One of the embodiments of the present invention relates to the improvement in the clarity of polyester/xylylene group containing polyamide blend bottles through a change in the process rather than a change in the materials used.
- the preferred blends are comprised of PET and MXD6 nylon. It is known in the art that the color in PET/MXD6 structures is due to the presence of catalyst residue in the polyester. This color can be controlled by limiting the amount of catalyst. Also, the orientation of PET and MXD6 during the manufacturing process (two stage injection—reheat blow molding) results in the development of haze caused by refractive index chances and the enlarged domains of MXD6.
- the present invention provides a solution to the problems of color and haze by using the extrusion blow-molding process and extrudable Polyester.
- the preferred polyester is PET.
- extrusion blow molding the bottle is produced when the polymer is in its molten state and therefore, the orientation is minimized. It is believed that he domain size of unoriented MXD6 is less than the wavelength of light and the refractive indices of PET and MXD6 are nearly the same. Thus, light passing through unoriented MXD6 structures does not scatter and produce haze.
- polyester/MXD6/cobalt blend is disposed between two polyester layers.
- the preferred polyester is PET.
- the cobalt octoate is present in an amount of up to 250 ppm.
- the preferred amount is 120 ppm.
- a three layer structure of the present invention having outer layers of PET and a core layer of MXD6 nylon/100 ppm cobalt octoate blend (wherein the core layer comprised 10% of the structure) was used to produce bottles on a Nissei stretch blow molding machine. Other bottles were produced by the same means and from similar material except the core layer did not contain cobalt. After the bottles were aged for three months at 0% relative humidity, they were tested for oxygen permeation. The results are shown below in table 5. TABLE 5 thickness oxygen permeation Variables (mils) (ccmil/m*2 day) (1) PET/MXD6/PET 27 42 (2) PET/MXD6 + 100 ppm Co/PET 28 9
- Flexible lidstock or pouches can be formed from coextruded film structures in accordance with the present invention having a core layer of a blend of MXD6 nylon and cobalt octoate disposed between two layers of nylon 6.
- the film was tested before and after retort for oxygen permeation at test conditions of 100% oxygen, 0% relative humidity (RH) and at 100% oxygen, 100% RH. The results are shown below in tables 6 and 7.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Laminated Bodies (AREA)
- Wrappers (AREA)
Abstract
Description
- This application is a continuation-in-part of application Ser. No. 07/472,400, filed Jan. 31, 1990, entitled “Improved Barrier Composition and Articles Made Therefrom”, incorporated herein by reference. The present invention relates to further improvements in the composition and articles of application Ser. No. 07/472,400.
- A continuation-in-part application, Ser. No. 07/761,490 entitled “Improved Barrier Composition and Articles Made Therefrom”, was filed on Sep. 18, 1991 as a continuation of application Ser. No. 07/472,400. Application Ser. No. 07/761,490 is incorporated herein by reference.
- Many products, particularly food products are sensitive to the presence of oxygen and/or the loss or absorption of water. These products are susceptible to deterioration, when packaged, due to oxygen and/or moisture absorption or loss through the wall of the package. Attempts to solve the problem have led to the widespread use of oxygen barriers and/or moisture barriers in packaging materials. Typical moisture barriers include polyethylene and polypropylene. Suitable oxygen barriers include EVOH, PVCH, Nylon and blends thereof. Vinylidene chloride—vinyl chloride copolymers and vinylidene chloride—methyl acrzlate copolymers are suitable as both moisture and oxygen barriers.
- A problem with conventional barrier materials is that due to their high cost or their unstable structural characteristics or other weaknesses, it is difficult to fabricate commercial packaging solely out of barrier materials. For instance, EVOH, while having superior oxygen barrier properties, suffers moisture problems because of the many hydroxyl groups in the polymer. Other barrier materials are so expensive that to manufacture structures solely from those barriers would be cost prohibitive. Accordingly, it has become a common practice to use multilayer structures, whereby, the amount of expensive or sensitive barrier material may be reduced to a thin layer and an inexpensive polymer can be used on one or both sides of the barrier layer as structural layers. In addition, the use of multilayer structures permits the barrier layer to be protected from Deterioration by structural layers on one or both sides of the barrier layer.
- Although multilayer structures containing a barrier layer may be cheaper and stronger than a single layer of barrier materials, such structures are more complicated to Manufacture than single-layered ones. In addition, multilayer structures comprised of layers of a variety of different materials may be opposed in some instances on environmental grounds, they may be more difficult to recycle since it is often difficult and expensive to separate the layers. In addition, reducing the thickness of the barrier layer in a multilayer structure can reduce the barrier properties of the film. Accordingly, there is a need for a single-layer packaging material with suitable barrier properties but without the cost or structural weaknesses of packaging made solely from a barrier material. There is also a need for additional multilayer structures having improved barrier properties wherein, the barrier material is reduced to a thinner layer and replace in part by inexpensive structural layers. These structures have the same barrier properties of prior art barriers but at lower cost due to a decrease in the amount of expensive barrier material used.
- In addition to barrier properties, it is frequently desirable to use materials which have oxygen absorption capabilities. These oxygen absorption or oxygen scavenging materials are useful in reducing the amount of oxygen that contaminate the product packaged in the container. An example of oxygen scavenging materials and methods of using them is disclosed in U.S. Pat. No. 4,425,410 to Farrell et al, the disclosure of which is hereby incorporated by reference herein. Another useful aspect of oxygen absorbing material is that such materials can reduce residual oxygen which is trapped in the headspace of a container during sealing, thereby preventing it from having a deleterious effect on the packaged products.
- A material that is commonly used in Packaging applications is polyethylene terephthalate resin, hereinafter referred to as PET. While PET has a number of valuable properties in packaging, it does not Stave as good a gas barrier property as is frequently required or desired in many applications. For example, although PET has good carbon dioxide barrier properties for soft drinks, it has not been found useful in packaging such products as beer because beer rapidly loses its flavor due to oxygen migration to the bottle. Similar problems are encountered with citrus products, tomato based products and aseptically packed meat. A packaging material with physical properties similar to PET is polyethylene naphthalate (PEN) which is 3-20 times more effective as a barrier but is considerably more expensive.
- In order to enhance polyester's gas barrier properties, polyesters have been used in a multilayer structure in combination with a layer having excellent gas barrier properties such as EVOH. However, multilayer structures employing polyester, such as PET, Frequently have adhesion problems between the polyester and the barrier layer which frequently leads to delamination over time.
- One approach to enhancing the gas barrier property of PET is to use a resin mixture which includes PET and a xylylene group containing polyamide resin. Such resin materials are disclosed in U.S. Pat. No. 4,501,781 to Kushida en al. One of the considerations encountered with such blends accordingly to Kushida is that there is a limit to the amount of xylylene group-containing polyamide resin that may be present in the PET blend. Kushida indicates that amounts of xylylene group-containing polyamide resin greater than 30% by weight causes the container to become a laminated foil structure which is susceptible to exfoliation between the foil layers of the container.
- According to Kushida, the permeation of oxygen gas through the walls of a container is less when the container is made with PET and a xylylene group-containing polyamide than when the container is made solely of PET. Kushida reports that a bottle shaped container made with PET-xylylene group-containing polyamide measured 0.0001 cc of oxygen Permeation per day compared to 0.0180 cc of oxygen permeation per day for a container made with PET.
- A preferred xylylene group-containing polyamide resin in the present invention is an aromatic polyamide formed by polymerizing meta-xylylene-diamine (H 2NCH2—m—C6H4—CH2NH2) with adipic acid (HO2C(CH2)4CO2H) . The most preferred such polymer is manufactured and sold by Mitsubishi Gas Chemicals, Japan, under the designation MXD6 or MXD6 nylon.
- In U.S. application Ser. No. 07/472,400 to Hong et al., the gas barrier property of polyester is enhanced by blending polyester with xylylene group-containing polyamide and a transition metal catalyst. Preferred embodiments include blends of PET/MXD6/Cobalt and exhibit superior oxygen barrier and oxygen absorption characteristics that were not present in the prior art structures. However, the structures in this invent-on are not as clear as the prior art structures. Hong discloses that it is believed that the high orientation of the blend increases the surface areas and interface between PET and MXD6 nylon so that there are a greater number of sites at which a reaction or an absorption of oxygen catalyzed by the transition metal catalyst takes place. This increased surface area and interface between PET and MXD6 nylon also causes a change in the refractive characteristics of the materials and results in an increased diffusion of light passing through the structures. The disclosures made in the Hong application are hereby incorporated by reference herein.
- In U.S. Pat. No. 4,407,873 to Christensen et al., the need for the proper selection of materials in films used in retort applications is discusses. Common to the requirements of retort pouch packaging is the requirement that the filled and sealed package be subjected to sterilizing conditions of relatively high temperature after the pouch is filled with product and sealed. Typical sterilizing conditions range in severity up to about 275° F. with residence times at that temperature of as much as 30 minutes or more. Such conditions impose severe stresses on the packages. Many packaging structures provide excellent protection for the package contents at less severe conditions. Or example, relatively simple packaging structures for packaging requiring the ability to withstand boiling water, such as at 212° F. are readily available from several suppliers. When sterilizing conditions are required, however, most of these packages fail to survive the processing. Typically, problems are encountered with excessive weakening or failure of the heat seals about the periphery of the couch. Also certain weaknesses or separations ray develop between the layers in the multiple layer sheet structure In addition, the high humidity experienced during the sterilizing process can change the chemical or structural properties of some materials.
- While Hong reports improved barrier properties using PET/MXD6/cobalt blends, there is a further need for oxygen barriers of greater clarity. In addition, there is a need for compositions which can be used in retort application in addition to acting as a clear oxygen barrier material thus, it is an object of the present invention to provide an improved monolayer barrier structure that satisfies both clarity and retort functions.
- It is also an object of the present invention to provide a clear monolayer barrier structure that has barrier properties superior to known barrier materials.
- It is a further object of the present invention to provide a multilayer structure having a layer comprising an MXD6/cobalt blend that does not delaminate under conditions of high relative humidity.
- FIG. 1 shows a pouch, sealed on three sides and made with the sheet structure of this invention.
- FIG. 2 shows a cross-section of the pouch of FIG. 1 taken at 2-2 of FIG. 1.
- FIG. 3 shows a cross-section of sheet structure used to form the pouch shown in FIGS. 1 and 2.
- It has been discovered that the oxygen barrier properties of MXD6 nylon are improved by the addition of cobalt octoate and that structures formed from MXD6/cobalt octoate blends and MXD6/cobalt octoate/PET blends have improved clarity and retort characteristics. The blends can be made into structures in the form of containers, films, sheets, pouches or lidstock. When used in a film, he MXD6/cobalt salt blend and the MXD6/cobalt salt/PET blend can be a single layer film or one layer of a multiple layer film which has been coextruded, extrusion coated or laminated.
- Although PET is the preferred polyester used in the MXD6/cobalt octoate/polyster blends, any thermoformable grade polyester with oxygen barrier qualities greater than those of polyolefins can be used.
- The addition of cobalt octoate to MXD6 nylon, or to a blend of MXD6 nylon and PET, produces blends that are significantly more impervious to oxygen than structures of MXD6 nylon or MXD6 nylon/PET blends. The improved barrier properties of the compositions of the present invention are unaffected by fluctuations of temperature and humidity. The oxygen barrier properties of previously known barrier polymers such as EVOH are adversely affected at 100% relative humidity RH) and so they must be protected by a moisture barrier polymer. In cue present invention, it has been discovered that the addition of cobalt octoate in an amount of up to about 250 ppm to a xylylene group-containing polyamide, preferably MXD6, or a xylylene group containing polyamide and polyester (preferably PET) blend produces a blend that does not require protection from 100% RH and thus, eliminates the need for a moisture barrier layer.
- Structures containing PET/MXD6/Cobalt oczoate blends or MXD6/cobalt octoate blends known in the art are oriented to increase oxygen barrier and oxygen absorption. However, such orientation ray have a deleterious effect on the color and clarity of the structure. These problems are caused by a change in the refractive index of the materials when the polymers are oriented. Orientation enlarges the domain size of MXD6 so that it is greater than the wavelength of light and this results in the increased scattering of light. See Table 1. In the present invention, knowledge of the processing and orientation characteristics of she MXD6/cobalt octoate blends and MXD6/cobalt octoate. PET blends is utilized to produce clear structures having improved oxygen barrier properties by limiting the degree of orientation so that the MXD6 domain increases in size up to less than the wavelength of light.
TABLE 1 THE EFFECT OF REFRACTIVE INDEX AND PARTICLE SIZE ON HAZE ORIENTATION REFRACTIVE INDEX PARTICLE NORMALIZED BLEND DRAWDOWN MXD 6 PET SIZE (um) HAZE (% HAZE/MIL) 0 1.580 1.578 0.1-0.3 0.2 9 1.589 1.620 2-4 0.8 - The oxygen barrier and oxygen absorbing compositions of the present invention can also be formed into multiple Layer structures. These multiple layer structures have a core layer of either a MXD6 nylon/cobalt octoate blend or a MXD6 nylon/polyester/cobalt octoate blend disposed between two adjacent layers. The two adjacent layers are comprised of either a Polyester or a polyamide. Also, one adjacent layer can be a polyester and the other adjacent layer can be a polyamide. In preferred embodiments, the polyester is PET and the polyamide is nylon 6. In another preferred embodiment, these structures are orientated to a degree so that the MXD6 domain increases in size up to less than the wavelength of light.
- In the present invention, any thermoformable grade polyester with oxygen barrier qualities greater than those of polyolefins, can be used to form clear packages and containers with almost zero oxygen permeability when blended with MXD6 and cobalt octzate. It has been discovered that the problem of haze is solved by extrusion blow molding the blend when it is in a molten state. This minimizes the orientation that occurs when the packages or containers are fabricated. By limiting the orientation, the domain sizes of the polyester and MXD6 do not increase to where they are greater than the wavelength of light and diffusion occurs.
- Table 2 shows a comparison of the amount of haze in bottles produced by extrusion blow molding and injection-reheat blow molding. The extrusion blow molded bottles display a significant reduction in the percent haze.
TABLE 2 COMPARISON OF THE HAZE OF INJECTION BLOW MOLDED AND EXTRUSION BLOW MOLDED BOTTLES NORMALIZED HAZE BOTTLES (% HAZE/MIL) INJECTION-REHEAT 3.16 BLOW MOLDED EXTRUSION BLOW 0.2 MOLDED-MATTE FINISH MOLD EXTRUSION BLOW 0.12 MOLDED-POLISHED MOLD - Cast film were prepared using Selar polyester which was blended with MXD6 nylon with and without the addition of cobalt octoate. In the presence of MXD6, these films showed a mild grey color. However, when these films were thermoformed, clear structures were produced. Moreover, haze was significantly reduced by minimizing the degree of orientation. Table 3 shows the normalized % haze/mil of materials compared to haze in injection-reheat blow molded bottles.
TABLE 3 MEASUREMENTS OF % HAZE/THICKNESS (% HAZE/MIL) Cast Film Formed Into Injection-Blow Cast Film Thermoformed Meat Molded Bottles Material Unoriented Packages Oriented Selar PT207 0.2 0.18 0.16 Selar PT207 + 0.25 0.3 3.16 7.5% MXD6 +120 PPM Cobalt - The composition of the present invention also comprises a blend of polyester, such a PET, and up to about 30% of a barrier material, such as a xylylene group-containing polyamide with about 49 ppm to about 110 ppm catalyst, most preferably in the form of a nascent catalyst residue from the PET. The barrier material is preferably a xylylene group-containing polyamide rein commonly known as MXD6 nylon which is available from Toyobo or Mitsubishi Gas Chemicals Company. The PET is available from Eastman Hoechst Celanese, ICI America, Shell Chemical or DuPont. The catalyst is a transition metal. Cobalt has been found to be Particularly useful in the present invention. Transition metal catalysts are defined as catalysts of metals which have filled or partially filled outer “d” orbitals or are those having filled “d” orbitals and filled or partially filled “p” orbitals.
- Multi-layer structures having a barrier layer of MXD6 nylon and two outer layers of PET wherein the MXD6 nylon comprises about 10 wt. % of the total structure will provide a clear film or ccrtainer. However, the oxygen barrier properties of such multilayer structures are not as good as blends of the present invention. In addition, such multiayer structures will not provide the oxygen absorption capabilities of the present invention.
- In blending the polyester with the oxygen barrier material, it is preferable that a physical blend of the pellets be made in a suitable mixing device. The process disperses the particles of he barrier material in the polyester. In one embodiment of the present invention, PET, MXD6 nylon and cobalt salt are mixed together in a screw extruder to form a blend. This extrusion is then oriented to a limited degree by extrusion blow-molding to form a structure such as a container or bottle. When barrier material is blended with polyester, the barrier material is normally present as spherical particles dispersed in PET.
- Containers made in accordance with this method are clear, unlike the prior art structures described above. However, these containers exhibit the same superior oxygen barrier and oxygen absorption characteristics of the prior art structures disclosed by Hong. In a second embodiment, a blend consisting of PET, up to about 30 wt. % MXD6 nylon (preferably up to 10 wt. % MXD6 nylon) and up to about 110 ppm cobalt salt is coextruded as a barrier Layer with a layer of PET on each surface thereof to form a three layer structure. In a preferred embodiment for example, the barrier layer would be a blend of 10 wt. % MXD6 nylon and the overall percentage of MXD6 nylon in the structure would be about 2 wt. %. Containers made from this structure are clear and do not exhibit the haze found in prior art containers. In addition, the catalyst in the blends of the present invention improves the barrier properties of structures made therefrom by providing oxygen absorption capabilities.
- It has been discovered that compositions of blends of a xylylene group—containing polyamide and up to 250 PPM of a transition metal catalyst do not have heir oxygen barrier characteristics adversely affected by the high relative humidity conditions experienced during retort. Therefore, they can be used to form films that do not require additional moisture barrier layers. The preferred blends of these compositions are comprised of MXD6 and cobalt octoate and they are used to form the oxygen barrier layer of a single or multiple layer film. When used in a multiple layer film, the barrier layer is disposed between two adjacent layers. One, or both, of the adjacent layers is comprised of a polyester or a polyamide. The preferred polyester As PET and the preferred polyamide is nylon 6. In one embodiment of the present invention, these compositions are oriented to a degree so that the MXD6 domain increases in size up to less than the wavelength of light.
- The invention will now be described in detail and in relation to the drawings. FIG. 1 illustrates a pouch such as is the desired packaging structure of one of the embodiments of this invention. A cross-section of a portion of the pouch is shown in FIG. 2. The sheet material used to make the pouch is seen in FIG. 3. By comparison of FIGS. 2 and 3 it is seen that the FIG. 2 construction consists of two sheet elements of the FIG. 3 construction in face to face relation with the
layers 12 joined at the one edge in heat seal. The pouch is formed by arranging the two sheet elements in face to face relationship and formingheat seals 19 about the common periphery. Alternately, the pouch may be formed by folding a sheet element onto itself and forming heat seals about the edges. Either way the formed pouch appears as shown in FIG. 1. - Referring now to FIGS. 2 and is,
layer 12 is a heat sealable layer comprised of a polyester or a polyamide.Layer 14 is an optional adhesive, or tie layer, selected based on the materials in the adjacent layers. Layer 16 a blend of a xylylene group-containing polyamide and up to 250 ppm of a transition metal catalyst.Layer 18 is also an optional adhesive, or tie, layer and is also selected based on the materials in the adjacent layers.Layer 20 is an outer protective layer comprised of a polyester or a polyamide. - The formed pouch is intended for packaging products which are subjected to a sterilizing process after the product is in the package and the package is sealed. A common sterilizing process is known as autoclave, or retort, processing. In this process, closed and sealed packages are placed in a pressure vessel. Steam and water are then introduced into the vessel at about 275° F. at a sufficiently high pressure to permit maintenance of the desired temperature. The temperature and pressure are usually maintained for about 30 minutes. Finally, the pressure vessel is cooled and the pressure temporarily maintained until the packages cool Internally. Finally the pressure is released and the processed packages are removed.
- Sheet structures of this invention generally range in thickness from about 3 mils up to about 10 mils. The thickest layer is usually the sealant layer and the thinnest layers usually are the tie layers and the oxygen barrier layer.
- The sheet structures of this invention may be made by conventional processes and combinations of processes. The process and its sequences may be selected according to the equipment and polymers available. The specific structure selected and the compositions of the oxygen barrier layer and the outer layers of polyester will be at least partially dependent on the process and its sequences.
- Both the orientation and the large amounts of catalysts used in prior art structures frequently had a deleterious effect on haze, color and other properties of the structure. These undesirable effects have been overcome in the present invention by controlling the degree of orientation and limiting the amount of catalyst to levels that do not change the refractive characteristics and color, respectively of the blend materials.
- Prior art structures that used cobalt as a catalyst tended to appear green in color. In the present invention, his problem has been solved by controlling the amount of cobalt added to the barrier blend material. The result is an improved structure that is clear and free from the green tint of the prior art structures.
- Although the detailed absorption/reaction mechanism Is not fully understood, concentrations of about 49 ppm to about 120 ppm residual catalyst in a polyester-barrier material blend, such as a PET-xylylene group-containing polyamide resin blend, have not only superior oxygen barrier properties but also significant oxygen scavenging capabilities.
- Thus, in the present invention there is provided a composition having superior oxygen barrier and oxygen absorption characteristics. This composition may be employed as a mono or multilayer film, such as, for example, in a pouch or flexible lidstock. These compositions may also be formed into rigid containers or may comprise the sidewall, body, lid or entire container. Also, the composition of the present invention may be formed into a chip and used in a container as an oxygen scavenger.
- A preferred embodiment of the present invention is a bend of PET and MXD6 nylon, wherein the MXD6 nylon is present in an amount of from about 2.5 weight % to about 15 weight % with the balance being PET. Cobalt is present in a range of 49 ppm to about 120 ppm with 62 ppm being most preferable. Another embodiment is pure MXD6 with between 49 and 120 ppm cobalt.
- In a more preferred embodiment, the MXD6 nylon is present in an amount of from about 4 weight % to about 10 weight % with the balance being PET. Cobalt is preferably present in the range of from about 49 ppm to about 120 ppm and most preferably present in an amount of about 62 ppm.
- In the most preferred embodiment, MXD6 nylon is present In the blend in an amount of about 7.5% with the remainder being PET and cobalt, present in the amounts stated above.
- In some PET, nascent cobalt is present as a residual of the PET polymerization catalyst. Specially added cobalt is preferably present as a cobalt salt dispersed in mineral spirits such as that sold under the trademark Nuodex by Huls America. The Nuodex products contain up to about 15% by weight cobalt. The preferred maximum amount of catalyst is about 250 ppm and is dependent on the structure being formed from the PET/MXD6/cobalt blends.
- The xylylene group containing polyamide is preferably a MXD6 nylon which is produced by condensation polymerization of metha-xylylene diamine (MXDA) and adipic acid.
- In biaxially orienting the blends of the present invention, it is preferred that the degree of orientation not exceed the limit at which the refractive characteristics of the blend materials change and the clarity of the structures deteriorates.
- In one of the embodiments of the invention, the multiple layer sheet structures have outer layers comprised of polyesters or polyamides that are suitable for heat sealing.
- In another embodiment, an adhesive layer is disposed on one or both sides of the barrier blend layer to bond the polyester or polyamide layers to the blend layer.
- One of the embodiments of the present invention relates to the improvement in the clarity of polyester/xylylene group containing polyamide blend bottles through a change in the process rather than a change in the materials used. The preferred blends are comprised of PET and MXD6 nylon. It is known in the art that the color in PET/MXD6 structures is due to the presence of catalyst residue in the polyester. This color can be controlled by limiting the amount of catalyst. Also, the orientation of PET and MXD6 during the manufacturing process (two stage injection—reheat blow molding) results in the development of haze caused by refractive index chances and the enlarged domains of MXD6.
- The present invention provides a solution to the problems of color and haze by using the extrusion blow-molding process and extrudable Polyester. The preferred polyester is PET. In extrusion blow molding, the bottle is produced when the polymer is in its molten state and therefore, the orientation is minimized. It is believed that he domain size of unoriented MXD6 is less than the wavelength of light and the refractive indices of PET and MXD6 are nearly the same. Thus, light passing through unoriented MXD6 structures does not scatter and produce haze.
- When multilayer, coextruded bottles are produced the polyester/MXD6/cobalt blend is disposed between two polyester layers. The preferred polyester is PET.
- The cobalt octoate is present in an amount of up to 250 ppm. The preferred amount is 120 ppm.
- Clear, non-hazy structures with PET/MXD6/cobalt blends have been successfully prepared using the extrusion blow-molding process. Multilayer, coextruded bottles having a core layer of 92.5% PET/7.5%. MXD6/120 ppm cobalt were successfully prepared using the process.
- As an example of this invention, cast films consisting of MXD6 nylon and 250 ppm cobalt octcate were prepared in thicknesses from 5 to 35 mils and were tested for oxygen permeations against cast films of MXD6 nylon without cobalt octoate. The results shown below in Table 4 demonstrate the improved oxygen barrier characteristics of films of MXD6 nylon and cobalt octoate.
TABLE 4 oxygen permeation (ccmil/m*2 day) (green cast films at 0% RH) thickness (hrs) Variables (mils) 36 84 180 276 324 I. MXD6 film 5 17 15 5 11 12 9 15 13 9 — — 19 30 12 12 — — 32 93 38 13 7 12 II. MXD6 5 8 3 1 0.3 0.5 film + 250 ppm 11 — 0 2 — — Co 19 23 1 2 — — 35 39 0 2 — — - A three layer structure of the present invention having outer layers of PET and a core layer of MXD6 nylon/100 ppm cobalt octoate blend (wherein the core layer comprised 10% of the structure) was used to produce bottles on a Nissei stretch blow molding machine. Other bottles were produced by the same means and from similar material except the core layer did not contain cobalt. After the bottles were aged for three months at 0% relative humidity, they were tested for oxygen permeation. The results are shown below in table 5.
TABLE 5 thickness oxygen permeation Variables (mils) (ccmil/m*2 day) (1) PET/MXD6/PET 27 42 (2) PET/MXD6 + 100 ppm Co/PET 28 9 - Flexible lidstock or pouches can be formed from coextruded film structures in accordance with the present invention having a core layer of a blend of MXD6 nylon and cobalt octoate disposed between two layers of nylon 6. The film was tested before and after retort for oxygen permeation at test conditions of 100% oxygen, 0% relative humidity (RH) and at 100% oxygen, 100% RH. The results are shown below in tables 6 and 7.
TABLE 6 (TEST CONDITIONS: 100% OXYGEN; 0% RH; UNAGED SAMPLE) TOTAL STEADY STATE THICKNESS PERMEATION SAMPLE (MILS) RATE* POST RETORT NYLON 6/1 MIL 3.53 6.2 MXD6+120 PPM Co/NYLON 6 PRE RETORT NYLON 6/2 MIL 4.44 0.1 MXD6+120 PPM Co/NYLON 6 POST RETORT NYLON 6/2 MIL 4.74 0.1 MXD6+120 PPM Co/NYLON 6 PRE RETORT NYLON 6/1 MIL 3.31 0.6 MXD6+250 PPM Co/NYLON 6 POST RETORT NYLON 6/1 MIL 3.38 3.2 MXD6+250 PPM Co/NYLON 6 PRE RETORT NYLON 6/2 MIL 4.50 0.2 MXD6+250 PPM Co/NYLON 6 POST RETORT NYLON 6/2 MIL 4.84 0.0 MXD6+250 PPM Co/NYLON 6 PRE RETORT NYLON 6 3.14 48.0 POST RETORT NYLON 6 2.88 39.4 -
TABLE 7 (TEST CONDITIONS: 100% OXYGEN; 100% RH; UNAGED SAMPLE) TOTAL STEADY STATE THICKNESS PERMEATION SAMPLE (MILS) RATE* POST RETORT NYLON 6/1 MIL 3.53 60.4 MXD6+120 PPM Co/NYLON 6 PRE RETORT NYLON 6/2 MIL 4.44 31.4 MXD6+120 PPM Co/NYLON 6 POST RETORT NYLON 6/2 MIL 4.74 2.6 MXD6+120 PPM Co NYLON 6 PRE RETORT NYLON 6/1 MIL 3.31 6.6 MXD6+250 PPM Co/NYLON 6 POST RETORT NYLON 6/1 MIL 3.38 22.4 MXD6+250 PPM Co/NYLON 6 PRE RETORT NYLON 6/2 MIL 4.50 2.6 MXD6+250 PPM Co/NYLON 6 POST RETORT NYLON 6/2 MIL 4.84 0.2 MXD6+250 PPM Co/NYLON 6 PRE RETORT NYLON 6 3.14 288 POST RETORT NYLON 6 2.88 314
Claims (70)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/941,873 US20020001684A1 (en) | 1990-01-31 | 1997-09-30 | Barrier compositions and articles made therefrom |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/472,400 US5281360A (en) | 1990-01-31 | 1990-01-31 | Barrier composition and articles made therefrom |
| US07/761,490 US5314987A (en) | 1990-01-31 | 1991-09-18 | Barrier compositions and film made therefrom having improved optical and oxygen barrier properties |
| US24806594A | 1994-05-23 | 1994-05-23 | |
| US08/941,873 US20020001684A1 (en) | 1990-01-31 | 1997-09-30 | Barrier compositions and articles made therefrom |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US24806594A Continuation | 1990-01-31 | 1994-05-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20020001684A1 true US20020001684A1 (en) | 2002-01-03 |
Family
ID=46246466
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/761,490 Expired - Lifetime US5314987A (en) | 1990-01-31 | 1991-09-18 | Barrier compositions and film made therefrom having improved optical and oxygen barrier properties |
| US08/941,873 Abandoned US20020001684A1 (en) | 1990-01-31 | 1997-09-30 | Barrier compositions and articles made therefrom |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/761,490 Expired - Lifetime US5314987A (en) | 1990-01-31 | 1991-09-18 | Barrier compositions and film made therefrom having improved optical and oxygen barrier properties |
Country Status (1)
| Country | Link |
|---|---|
| US (2) | US5314987A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040043233A1 (en) * | 2002-08-27 | 2004-03-04 | Cryovac, Inc. | Dual-ovenable, heat-sealable packaging film |
| US20040121049A1 (en) * | 2002-12-18 | 2004-06-24 | Cryovac, Inc. | Dual-ovenable, heat-sealable packaging tray |
| US20040121054A1 (en) * | 2002-12-20 | 2004-06-24 | Berrier Arthur L. | Method of preparing food |
| US20040224111A1 (en) * | 2003-01-31 | 2004-11-11 | Sisson Edwin A. | Article comprising light absorbent composition to mask visual haze and related methods |
| US20100247935A1 (en) * | 2009-03-24 | 2010-09-30 | Baxter International Inc. | Non-pvc films having barrier layer |
| EP2366734A1 (en) | 2005-10-07 | 2011-09-21 | M & G Polimeri Italia S.P.A. | Polyamides and polyesters blended with a lithium salt interfacial tension reducing agent |
| US20110262668A1 (en) * | 2010-04-27 | 2011-10-27 | Graham Packaging Company, L.P. | Delamination resistant multilayer containers |
| US9988198B2 (en) | 2010-08-23 | 2018-06-05 | Cryovac, Inc. | Ovenable heat-sealed package |
Families Citing this family (57)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2207439B (en) * | 1987-07-27 | 1992-02-12 | Metal Box Plc | Improvements in and relating to packaging |
| US20030134966A1 (en) * | 1990-01-31 | 2003-07-17 | Kim Yong Joo | Barrier compositions and articles made therefrom |
| WO1995011801A1 (en) * | 1993-10-25 | 1995-05-04 | American National Can Company | Improved barrier compositions and articles made therefrom |
| ES2196096T3 (en) * | 1994-12-14 | 2003-12-16 | Continental Pet Technologies | TRANSPARENT CONTAINER CONTAINING AN ALIFATIC POLYETHONE OXYGEN SUPPRESSION AGENT. |
| US5759653A (en) * | 1994-12-14 | 1998-06-02 | Continental Pet Technologies, Inc. | Oxygen scavenging composition for multilayer preform and container |
| US6162857A (en) | 1997-07-21 | 2000-12-19 | Eastman Chemical Company | Process for making polyester/platelet particle compositions displaying improved dispersion |
| US6486252B1 (en) | 1997-12-22 | 2002-11-26 | Eastman Chemical Company | Nanocomposites for high barrier applications |
| EP1054925B1 (en) * | 1998-02-03 | 2011-10-12 | Graham Packaging PET Technologies Inc. | Enhanced oxygen-scavenging polymers, and packaging made therefrom |
| US20020037377A1 (en) | 1998-02-03 | 2002-03-28 | Schmidt Steven L. | Enhanced oxygen-scavenging polymers, and packaging made therefrom |
| US20040005475A1 (en) * | 1998-04-17 | 2004-01-08 | Curie Kevin James | Transparent multilayer polypropylene container with barrier protection |
| US6677013B1 (en) * | 1998-04-17 | 2004-01-13 | Pechiney Emballage Flexible Europe | Transparent multilayer polypropylene container with barrier protection |
| WO2000034375A1 (en) | 1998-12-07 | 2000-06-15 | Eastman Chemical Company | A polymer/clay nanocomposite comprising a clay mixture and a process for making same |
| WO2000034378A1 (en) * | 1998-12-07 | 2000-06-15 | Eastman Chemical Company | Polymer/clay nanocomposite and process for making same |
| US6417262B1 (en) | 1998-12-07 | 2002-07-09 | Eastman Chemical Company | High barrier amorphous polyamide-clay nanocomposite and a process for preparing same |
| CA2353966A1 (en) * | 1998-12-07 | 2000-06-15 | Sam Richard Turner | Process for preparing an exfoliated, high i.v. polymer nanocomposite with an oligomer resin precursor and an article produced therefrom |
| BR9916039A (en) | 1998-12-07 | 2001-12-04 | Eastman Chem Co | Polymer-clay nanocomposite, article, composition, and process for the preparation of a polymer-clay nanocomposite |
| US6548587B1 (en) | 1998-12-07 | 2003-04-15 | University Of South Carolina Research Foundation | Polyamide composition comprising a layered clay material modified with an alkoxylated onium compound |
| US6552114B2 (en) | 1998-12-07 | 2003-04-22 | University Of South Carolina Research Foundation | Process for preparing a high barrier amorphous polyamide-clay nanocomposite |
| NZ514992A (en) * | 1999-04-16 | 2003-11-28 | Pechiney Emballage Flexible Eu | Transparent multilayer polypropylene container with barrier protection |
| BR0012815A (en) | 1999-07-30 | 2002-05-07 | Eastman Chem Co | Mixture of polymer, article, and method to reduce permeability to polyester gas |
| US6777479B1 (en) | 1999-08-10 | 2004-08-17 | Eastman Chemical Company | Polyamide nanocomposites with oxygen scavenging capability |
| US6610772B1 (en) | 1999-08-10 | 2003-08-26 | Eastman Chemical Company | Platelet particle polymer composite with oxygen scavenging organic cations |
| US6486253B1 (en) | 1999-12-01 | 2002-11-26 | University Of South Carolina Research Foundation | Polymer/clay nanocomposite having improved gas barrier comprising a clay material with a mixture of two or more organic cations and a process for preparing same |
| JP2003515648A (en) | 1999-12-01 | 2003-05-07 | イーストマン ケミカル カンパニー | Polymer-clay nanocomposites containing amorphous oligomers |
| US6737464B1 (en) | 2000-05-30 | 2004-05-18 | University Of South Carolina Research Foundation | Polymer nanocomposite comprising a matrix polymer and a layered clay material having a low quartz content |
| JP2003535204A (en) | 2000-05-30 | 2003-11-25 | ユニバーシティ オブ サウスカロライナ リサーチ ファウンデーション | Polymer nanocomposites containing matrix polymers and layered clay materials with improved levels of extractables |
| KR20040050926A (en) * | 2001-10-24 | 2004-06-17 | 페쉬니 앙발라쥬 플렉서블 유럽 | Polypropylene container and process for making it |
| US6953768B2 (en) * | 2002-11-26 | 2005-10-11 | Teck Cominco Metals Ltd. | Multi-component catalyst system for the polycondensation manufacture of polyesters |
| DE10302033A1 (en) * | 2003-01-21 | 2004-07-29 | Mitsubishi Polyester Film Gmbh | Polyester film with improved oxygen barrier and poly (m-xylene-adipinamide) -containing cover layer, process for its production and its use |
| US7526108B2 (en) * | 2003-02-11 | 2009-04-28 | Topaz Systems, Inc. | Wireless data management system |
| CN1787904B (en) * | 2003-05-14 | 2010-05-26 | 三菱树脂株式会社 | Fluororesin laminated film and process for producing the same |
| US20050009976A1 (en) * | 2003-07-10 | 2005-01-13 | Honeywell International, Inc. | Delamination-resistant, barrier polyamide compositions for 3-layer pet beverage bottles |
| EP1504999A1 (en) * | 2003-08-05 | 2005-02-09 | Amcor Limited | Rigid plastic container having gas-barrier properties and high transparency |
| US20050069694A1 (en) * | 2003-09-26 | 2005-03-31 | Gilder Stephen D. | Anti-microbial carpet underlay and method of making |
| US20050159526A1 (en) * | 2004-01-15 | 2005-07-21 | Bernard Linda G. | Polymamide nanocomposites with oxygen scavenging capability |
| US8192676B2 (en) | 2004-02-12 | 2012-06-05 | Valspar Sourcing, Inc. | Container having barrier properties and method of manufacturing the same |
| DE102004030978A1 (en) * | 2004-06-26 | 2006-01-19 | Mitsubishi Polyester Film Gmbh | Adhesive polyester film containing poly (m-xyleneadipamide) |
| DE102004030980A1 (en) * | 2004-06-26 | 2006-01-19 | Mitsubishi Polyester Film Gmbh | Polyester film containing poly (m-xyleneadipamide) |
| DE102004030977A1 (en) * | 2004-06-26 | 2006-01-19 | Mitsubishi Polyester Film Gmbh | Metallized or ceramic-coated polyester film containing poly (mxyloladipinamide) |
| DE602005009210D1 (en) | 2004-08-17 | 2008-10-02 | Invista Tech Sarl | COLORED OXYGEN-ABSORBING POLYMERS |
| US20060099362A1 (en) * | 2004-11-05 | 2006-05-11 | Pepsico, Inc. | Enhanced barrier packaging for oxygen sensitive foods |
| US20070039268A1 (en) * | 2004-12-01 | 2007-02-22 | L&P Property Management Company | Energy Absorptive/Moisture Resistive Underlayment Formed using Recycled Materials and a Hard Flooring System Incorporating the Same |
| US20060144012A1 (en) * | 2004-12-01 | 2006-07-06 | Norman Manning | Recycled energy absorbing underlayment and moisture barrier for hard flooring system |
| JP2008523170A (en) * | 2004-12-06 | 2008-07-03 | イーストマン ケミカル カンパニー | Polyester-based cobalt concentrate for oxygen scavenging compositions |
| BRPI0517151A (en) * | 2004-12-06 | 2008-09-30 | Constar Int Inc | fused formulated polyester polymer composition, process for producing an article, isolated solid and solid concentrate |
| US7375154B2 (en) * | 2004-12-06 | 2008-05-20 | Eastman Chemical Company | Polyester/polyamide blend having improved flavor retaining property and clarity |
| MX2007014612A (en) * | 2005-05-18 | 2008-01-17 | M & G Polimeri Italia Spa | Polyester composition. |
| US8124204B2 (en) * | 2005-07-08 | 2012-02-28 | Mitsubishi Gas Chemical Company, Inc. | Multi-layered bottle |
| US8080191B2 (en) * | 2006-10-20 | 2011-12-20 | Pepsico, Inc. | Extrudable polyethylene terephthalate blend |
| US20080161529A1 (en) * | 2006-12-28 | 2008-07-03 | Jason Christopher Jenkins | Oxygen-scavenging polyesters useful for packaging |
| US7521523B2 (en) * | 2006-12-28 | 2009-04-21 | Eastman Chemical Company | Oxygen-scavenging polyester compositions useful in packaging |
| US20080226852A1 (en) * | 2007-03-16 | 2008-09-18 | Weyerhaeuser Co. | Gas barrier packaging board |
| US20080226851A1 (en) * | 2007-03-16 | 2008-09-18 | Weyerhaeuser Co. | Gas barrier packaging board |
| US20080299403A1 (en) * | 2007-06-01 | 2008-12-04 | Weyerhaeuser Co. | Gas barrier packaging board |
| US20100252101A1 (en) * | 2007-11-16 | 2010-10-07 | Okura Industrial Co. Ltd | Back protective sheet for solar cell module and solar cell module protected thereby |
| ES2718245T3 (en) | 2008-04-18 | 2019-06-28 | Pepsico Inc | Polyester compositions and procedure for preparing articles by extrusion and blow molding |
| CN102408683A (en) * | 2011-08-05 | 2012-04-11 | 江阴市龙山合成材料有限公司 | Glass fiber reinforced halogen hydrolysis-resistant flame-retardant PBT (polybutylene terephthalate) and preparation method thereof |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4433117A (en) * | 1982-03-23 | 1984-02-21 | Kuraray Co., Ltd. | Copolyesteramide and production of the same |
| WO1989001012A1 (en) * | 1987-07-27 | 1989-02-09 | Mb Group Plc | Improvements in and relating to packaging |
-
1991
- 1991-09-18 US US07/761,490 patent/US5314987A/en not_active Expired - Lifetime
-
1997
- 1997-09-30 US US08/941,873 patent/US20020001684A1/en not_active Abandoned
Cited By (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7504158B2 (en) | 2002-08-27 | 2009-03-17 | Cryovac, Inc. | Dual-ovenable, heat-sealable packaging film |
| US6979494B2 (en) | 2002-08-27 | 2005-12-27 | Cryovac, Inc. | Dual-ovenable, heat-sealable packaging film |
| US20060088678A1 (en) * | 2002-08-27 | 2006-04-27 | Berrier Arthur L | Dual-ovenable, heat-sealable packaging film |
| US20040043233A1 (en) * | 2002-08-27 | 2004-03-04 | Cryovac, Inc. | Dual-ovenable, heat-sealable packaging film |
| US20040121049A1 (en) * | 2002-12-18 | 2004-06-24 | Cryovac, Inc. | Dual-ovenable, heat-sealable packaging tray |
| US7919161B2 (en) | 2002-12-18 | 2011-04-05 | Cryovac, Inc. | Dual-ovenable, heat-sealable packaging tray |
| US20040121054A1 (en) * | 2002-12-20 | 2004-06-24 | Berrier Arthur L. | Method of preparing food |
| US20100316825A1 (en) * | 2003-01-31 | 2010-12-16 | Edwin Andrew Sisson | Article Comprising Light Absorbent Composition to Mask Visual Haze and Related Methods |
| US8110264B2 (en) | 2003-01-31 | 2012-02-07 | M&G Usa Corporation | Article comprising light absorbent composition to mask visual haze and related methods |
| US20070138707A1 (en) * | 2003-01-31 | 2007-06-21 | Sisson Edwin A | Process to Make an Article Comprising Light Absorbent Composition to Mask Visual Haze and Related Methods |
| EP1590398B2 (en) † | 2003-01-31 | 2017-03-29 | M&G USA Corporation | Article comprising light absorbent composition to mask visual haze and related methods |
| US7833595B2 (en) * | 2003-01-31 | 2010-11-16 | M&G Usa Corporation | Article comprising light absorbent composition to mask visual haze and related methods |
| US20100316827A1 (en) * | 2003-01-31 | 2010-12-16 | Edwin Andrew Sisson | Article Comprising Light Absorbent Composition to Mask Visual Haze and Related Methods |
| US20100316826A1 (en) * | 2003-01-31 | 2010-12-16 | Edwin Andrew Sisson | Article Comprising Light Absorbent Composition to Mask Visual Haze and Related Methods |
| US20070128390A1 (en) * | 2003-01-31 | 2007-06-07 | Simone Ferrero | Article Comprising Light Absorbent Composition to Mask Visual Haze and Related Methods |
| US20100323137A1 (en) * | 2003-01-31 | 2010-12-23 | Edwin Andrew Sisson | Article Comprising Light Absorbent Composition to Mask Visual Haze and Related Methods |
| US20040224111A1 (en) * | 2003-01-31 | 2004-11-11 | Sisson Edwin A. | Article comprising light absorbent composition to mask visual haze and related methods |
| US9266638B2 (en) | 2003-01-31 | 2016-02-23 | M&G Usa Corporation | Article comprising light absorbent composition to mask visual haze and related method |
| US8999468B2 (en) | 2003-01-31 | 2015-04-07 | M&G Usa Corporation | Article comprising light absorbent composition to mask visual haze and related method |
| US8053050B2 (en) | 2003-01-31 | 2011-11-08 | M&G Usa Corporation | Article comprising light absorbent composition to mask visual haze and related methods |
| US8052917B2 (en) | 2003-01-31 | 2011-11-08 | M&G Usa Corporation | Process to make an article comprising light absorbent composition to mask visual haze and related methods |
| US8057874B2 (en) | 2003-01-31 | 2011-11-15 | M&G Usa Corporation | Article comprising light absorbent composition to mask visual haze and related methods |
| US8067074B2 (en) | 2003-01-31 | 2011-11-29 | M&G Usa Corporation | Article comprising light absorbent composition to mask visual haze and related methods |
| US7438960B2 (en) | 2003-01-31 | 2008-10-21 | M & G Usa Corporation | Article comprising light absorbent composition to mask visual haze and related methods |
| US8927076B2 (en) | 2003-01-31 | 2015-01-06 | M&G Usa Corporation | Article comprising light absorbent composition to mask visual haze and related method |
| EP2366734A1 (en) | 2005-10-07 | 2011-09-21 | M & G Polimeri Italia S.P.A. | Polyamides and polyesters blended with a lithium salt interfacial tension reducing agent |
| US20100247935A1 (en) * | 2009-03-24 | 2010-09-30 | Baxter International Inc. | Non-pvc films having barrier layer |
| US8822001B2 (en) * | 2010-04-27 | 2014-09-02 | Graham Packaging Company, L.P. | Delamination resistant multilayer containers |
| US20110262668A1 (en) * | 2010-04-27 | 2011-10-27 | Graham Packaging Company, L.P. | Delamination resistant multilayer containers |
| US9988198B2 (en) | 2010-08-23 | 2018-06-05 | Cryovac, Inc. | Ovenable heat-sealed package |
Also Published As
| Publication number | Publication date |
|---|---|
| US5314987A (en) | 1994-05-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US6239210B1 (en) | Barrier compositions and articles made therefrom | |
| US20020001684A1 (en) | Barrier compositions and articles made therefrom | |
| US20050106343A1 (en) | Barrier compositions and articles made therefrom | |
| US5866649A (en) | Barrier compositions and articles made therefrom | |
| RU2189337C2 (en) | Thermoplastic container for food products, thermoplastic and method of its manufacturing, multilayer thermoplastic container | |
| EP3946758B1 (en) | Recyclable film for thermoforming | |
| US5804236A (en) | Oxygen scavenging container | |
| EP1413429B1 (en) | Gas-barrier multi-layer structure | |
| AU692480B2 (en) | Improved barrier compositions and articles made therefrom | |
| EP2898012B1 (en) | Oxygen scavenging plastic material | |
| EP1752286B1 (en) | Gas-barrier multilayer structure and process for producing the same | |
| EP2057012A2 (en) | Pctfe film with extrusion coating of eva or eva with uv absorbers | |
| EP0580360A1 (en) | Multilayer container | |
| CA2175051C (en) | Barrier compositions and articles made therefrom | |
| ES2328243T3 (en) | POLYMER PACKAGING COAT WITH IMPROVED SEPARATION PROPERTIES. | |
| WO1998013266A9 (en) | Transparent oxygen-scavenging article including biaxially-oriented polyester | |
| EP2915842A1 (en) | Oxygen scavenging composition for plastic material | |
| CA2356355C (en) | Improved active oxygen scavenger packaging | |
| EP3774336B1 (en) | Autoclavable barrier film | |
| EP2535185B1 (en) | Multilayer film made of recyclable plastic material, container comprising said film and related package | |
| JPH03503867A (en) | Improvements in and related to packaging | |
| EP0919365B1 (en) | Composite sheet and sealed container | |
| US5439718A (en) | Multilayer container of polycarbonate and amorphous polyamide of improved barrier and stress crack resistant properties | |
| JP2002234127A (en) | Multilayered molded object |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: PECHINEY PLASTIC PACKAGINC, INC., ILLINOIS Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:AMERICAN NATIONAL CAN COMPANY;REEL/FRAME:012463/0131 Effective date: 20011112 |
|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |
|
| AS | Assignment |
Owner name: PECHINEY EMBALLAGE FLEXIBLE EUROPE, FRANCE Free format text: RESUBMISSION OF DOCUMENT ID NO 102198992;ASSIGNOR:PECHINEY PLASTIC PACKAGING, INC.;REEL/FRAME:013467/0484 Effective date: 20020117 |