Packaging and method of making packaging
09610755 ยท 2017-04-04
Assignee
Inventors
Cpc classification
B32B27/322
PERFORMING OPERATIONS; TRANSPORTING
Y10T428/31797
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
Y10T428/31743
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
B32B2255/10
PERFORMING OPERATIONS; TRANSPORTING
B32B27/16
PERFORMING OPERATIONS; TRANSPORTING
B32B27/28
PERFORMING OPERATIONS; TRANSPORTING
Y10T428/31928
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
B32B2270/00
PERFORMING OPERATIONS; TRANSPORTING
B32B7/12
PERFORMING OPERATIONS; TRANSPORTING
B32B27/306
PERFORMING OPERATIONS; TRANSPORTING
Y10T428/31895
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
B32B29/00
PERFORMING OPERATIONS; TRANSPORTING
B32B27/308
PERFORMING OPERATIONS; TRANSPORTING
B32B29/002
PERFORMING OPERATIONS; TRANSPORTING
Y10T428/3192
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
Y10T428/31909
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
B32B2307/546
PERFORMING OPERATIONS; TRANSPORTING
B32B27/327
PERFORMING OPERATIONS; TRANSPORTING
Y10T428/31855
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
International classification
B32B7/12
PERFORMING OPERATIONS; TRANSPORTING
B32B37/02
PERFORMING OPERATIONS; TRANSPORTING
B32B37/00
PERFORMING OPERATIONS; TRANSPORTING
B32B27/30
PERFORMING OPERATIONS; TRANSPORTING
B32B29/00
PERFORMING OPERATIONS; TRANSPORTING
B32B27/16
PERFORMING OPERATIONS; TRANSPORTING
B32B27/28
PERFORMING OPERATIONS; TRANSPORTING
Abstract
Packaging and a method of making the packaging is disclosed. The packaging includes a substrate with an asymmetrical coextrusion attached there to. The coextrusion includes an ethylene vinyl alcohol layer that is disposed toward the substrate.
Claims
1. A method of making packaging, the method comprising: providing a substrate; extruding an asymmetrical coextrusion including an ethylene vinyl alcohol layer and at least one support layer, wherein the ethylene vinyl alcohol layer has a first face and a second face, wherein the first face is supported by the at least one support layer during the extrusion and wherein the second face does not interface with any other layer of the asymmetrical coextrusion; and attaching the second face of the ethylene vinyl alcohol layer of the asymmetrical coextrusion to the substrate to form the packaging.
2. The method of claim 1, further comprising the step of applying a polymeric barrier layer to at least a portion of at least one side of the substrate before attaching the second face of the ethylene vinyl alcohol layer of the asymmetrical coextrusion to the substrate to form the packaging.
3. The method of claim 2, wherein the second face of the ethylene vinyl alcohol layer is directly attached to the polymeric barrier layer.
4. The method of claim 2, further comprising the step of treating a surface of the polymeric barrier layer prior to attaching the second face of the ethylene vinyl alcohol layer of the asymmetrical coextrusion to the substrate to form the packaging.
5. The method of claim 4, wherein the step of treating includes flame treating the surface.
6. The method of claim 4, wherein the step of treating includes corona treating the surface.
7. The method of claim 4, wherein the step of treating includes liquid priming the surface.
8. The method of claim 2, wherein the polymeric barrier layer is low density polyethylene.
9. The method of claim 2, wherein the polymeric barrier layer includes at least one of low density polyethylene, medium density polyethylene, high density polyetheylene, linear low-density polyethylene, and metallocene catalyzed linear low density polyethylene.
10. The method of claim 2, wherein the polymeric barrier layer includes at least one of polypropylene, ethylene vinyl acetate resin, IONOMER, Nylon, ethylene acrylic acid copolymer (EAA), ethylene methacrylic acid copolymer (EMAA), ethylene methyl acrylate copolymer (EMAC), and ethylene n-butyl acrylate copolymer (EnBA).
11. The method of claim 1, wherein the substrate comprises paper.
12. The method of claim 1, wherein the substrate comprises a clear or metallized film selected from the group consisting of polyethylene terephthalate, oriented polypropylene (OPP), nylon, and polylactic acid (PLA) films.
13. The method of claim 1, wherein the one or more support layers includes a tie resin layer and a sealant layer.
14. The method of claim 1, wherein the one or more support layers includes a layer formed of a tie resin and a sealant blended together to form a tie sealant resin blend layer.
15. The method of claim 14, wherein the asymmetrical coextrusion is a two layer coextrusion including the ethylene vinyl alcohol layer and said tie sealant resin blend layer.
16. The method of claim 15, wherein the asymmetrical coextrusion is formable using a two resin capable coextruder.
17. The method of claim 13, wherein the tie resin layer is disposed between the ethylene vinyl alcohol layer and the sealant layer.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1)
(2)
DETAILED DESCRIPTION OF THE INVENTION
(3) Disclosed below are structures for a packaging containing EVOH which do not require complex coextrusion machinery configurations capable of forming five layer coextrusions. As used herein, a - is used to indicate layers that are coextruded with one another and / is used to indicate layers that are separated attached to one another.
(4) Now with reference to
(5) (1) PAPER/LDPE/EVOH-TSRB
(6) (2) PAPER/LDPE/EVOH-TIE-SEALANT
(7) (3) PET FILM/LDPE/EVOH-TSRB
(8) As used herein, TSRB refers to a tie resin and sealant resin blend in which the tie resin and sealant are blended together such that the blend may be coextruded as a single layer, whereas EVOH-TIE-SEALANT refers to three discrete separately formed layers of EVOH, tie resin (which is a type of resin designed to adhere the EVOH and the sealant layers together), and sealant. With respect to the figures, like reference numerals are used to describe like items in which the hundreds digit has been increased to correspond to the figure number (e.g., TSRB layer 110 corresponds to TSRB layer 310).
(9) Looking first at
(10) It is contemplated that the paper substrate may be a paper of a type having a machine glazed (MG) or a machine finished (MF) type finish, may be clay coated paper, may be of a white or a natural color, and may be of a Kraft, ground wood, recycled, or sulfite furnish. The paper may include laminations of one or more layers of paper or include a clear or metallized PET, oriented polypropylene (OPP), Nylon, or PLA film laminated to the paper.
(11) In one preferred form, the polymeric barrier layer is low density polyethylene (LDPE). However, the polymeric barrier layer on the paper may alternatively be MDPE, HDPE, LLDPE, POP (polyolefin plastomer), mLLDPE, or blends thereof as well as coextrusions thereof. Additives such as colors can be used. Other resins can be used in place of LDPE such as PP, EVA, IONOMER, Nylon, EAA, EMAA, EMAC, EnBA, and the like. If needed, EVOH tie resin can be blended into the poly layer for improved adhesion, especially if PP or HDPE is used in place of LDPE. In all cases, the materials used for the polymeric barrier layer are not extruded from the extruders used to make the asymmetrical EVOH coextrusion.
(12) To ensure good adhesion, the paper and/or polymeric barrier layers may be subjected to flame treatment, corona treatment, or other such priming to ready the surfaces for attachment.
(13) With respect to the specific chemical composition of the layers, the ethylene vinyl alcohol may be 35 mol % ethylene EVOH (available as EVAL C109B from Eval Company of America) and the TSRB may be 50% POP (polyolefin plastomer, available as DOW PT1450 from Dow Chemical Company), 25% tie resin (such as ADMER AT1000A available from Mitsui Chemicals America, Inc.), and 25% LDPE (low-density polyethylene, available as CHEVRON 1013 available from Chevron Chemical). The exact percentages of the constituent components may be varied depending on the temperatures, times, and pressures used to form the heat seal and the quality of the seal desired. Although EVOH with 35 mol % or higher ethylene content is believed to provide the best results, EVOH is available in 24% ethylene to 48% ethylene content. It is contemplated that any amount of ethylene content might be used or selected based on the desired properties of the barrier or for appropriate economy. Generally speaking, the lower the ethylene content, the better the aroma and oxygen barrier provided by the EVOH layer. It is contemplated that the basis weight of the EVOH layer may be in the range of 0.1#/3,000 ft.sup.2 to 10.0#/3,000 ft.sup.2.
(14) The TSRB may have a tie resin content from 10 wt % to 80 wt % and a polyethylene content from 20 wt % to 90 wt %. The tie resin may be an anhydride modified LDPE based adhesive resin concentrate such as ADMER AT1000A or DUPONT BYNEL 41E170. The polyethylene sealant resin may be LDPE, MDPE, HDPE, LLDPE, POP, mLLDPE and blends thereof, and copolymers of polyethylene such as, for example: EVA, IONOMER, EAA, EMAA, EMAC, EnBA, and the like. TSRB can be further modified with slip, antiblock, or color concentrates depending upon customer needs.
(15) The particular tie sealant resin blend selected may be configured to maximize the quality of the seal. The basis weight of the TSRB layer may be in the range of 1.0#/3,000 ft.sup.2 to 30.0#/3,000 ft.sup.2 and modified to provide enough TSRB material to form a robust seal.
(16) In order to achieve a thin and stable coating layer, EVOH is not extrusion coated as its own single layer, but can be coextruded with the TSRB or, as will be described with respect to structures (2) and (3) below, the tie resin and sealant layers. Of course, a benefit of using the tie sealant resin blend as in structures (1) and (3) is that a three resin capable coextruder is not required, but a two resin capable coextruder will be sufficient. In contrast, standard three resin, five layer EVOH extrusion coating production would require a more complex and costly coextruder, and add sealant and tie resin layers to the inside of the EVOH layer which have been rendered unnecessary by the inclusion of the polymeric barrier coating on the substrate which serves as a moisture barrier on that side of the EVOH layer.
(17) Turning now to
(18) Now with reference to
(19) In alternative forms, the PET film in structure (3) might alternatively be any kind of clear or metalized polyethylene terephthalate, polypropylene, nylon, or PLA (polylactic acid) film.
(20) Looking at the structures (1)-(3) above, it can be seen that the EVOH coextrusion is asymmetrical in all forms, unlike the LDPE-Tie Resin-EVOH-Tie Resin-LDPE structures which have been previously produced. Now, when extruded, the EVOH layer is initially at least partially exposed with one side of the layer being supported and protected by either the tie sealant resin blend layer or the tie resin and sealant layers. As will be described in more detail below with respect to the method of making the packaging, this initially exposed side of the EVOH layer is attached or laminated to the substrate, or polymeric barrier coating thereon, such that this exposed face is no longer exposed.
(21) It should be appreciated that in all three structures (1) through (3), the initially-exposed face of the EVOH layer is attached to a polymeric barrier layer which helps to protect that side of the EVOH layer from moisture. While this polymeric barrier layer is preferable for many applications, it is also contemplated that the polymeric barrier layer may be eliminated and the EVOH layer directly attached to the paper substrate or PET film substrate. To some extent, the removal of the polymeric barrier layer will increase the exposure of the EVOH layer to moisture which increases the rate of oxygen or aroma transmission through the EVOH layer. However, the PET film substrate may, at least to some degree, serve as a moisture barrier. Accordingly, by increasing either the substrate thickness and/or the EVOH layer thickness, the integrity of the product may be preserved for a longer period of time, even in the absence of the polymeric barrier layer. If the product to be housed in the packaging does not require good moisture vapor barrier, then it may be acceptable to remove the polymeric barrier layer.
(22) These structures provide a number of advantages over known flexible packaging solutions. In applications where a moderate oxygen barrier is required, EVOH provides good oxygen barrier at a lower cost than Al foil, metallized PET (MPET) film, and PVDC (polyvinylidene chloride) coated PET or OPP films. Further, for those applications which previously included PVDC in the packaging materials as a barrier material, the EVOH replaces the PVDC coated flexible packaging materials with a product that can be incinerated without worries of producing hydrochloric acid or other chlorinated hydrocarbon fumes into the air.
(23) In one preferred form for the packaging, the packaging has a structure of 25# PAPER/10# LDPE/4# EVOH-7# TSRB. (#/ream is based on a 3,000 ft.sup.2 ream size) The paper basis weight can range from 9#/ream to 100#/ream. The paper may be Kraft paper with a machine glaze type finish and of bleached white color which may be flame treated for good adhesion of the LDPE to the paper. The LDPE may be corona treated for good adhesion of the EVOH coextrusion to the LDPE coated paper. The LDPE for the polymeric layer (Chevron 4517) would be of slightly higher density than the LDPE used in the TSRB (Chevron 1013). This will provide improved moisture barrier for protection of the EVOH, while the LDPE used in the TSRB would be optimized for heat seal properties. The EVOH in the 4# EVOH-7# TSRB coextrusion is 35 mol % ethylene EVOH. However, for other applications the composition of the TSRB in the coextrusion may be tweaked. In this form, the TSRB may be 25% tie resin (ADMER AT1000A) and 75% LDPE (CHEVRON 1013). Even though a LDPE layer is present between the paper and the EVOH, it should be appreciated that the EVOH-TSRB coextrusion is formed from a single die and this part of the structure does not require more than a two resin coextruder station.
(24) Some specific additional variations are provided below with respect to the disclosed structures. According to one form, the structure of the packaging material is 25# PAPER/10# LDPE/4# EVOH-1.5# TIE-5.5# PE SEALANT. In another form, the structure of the packaging material is 25# PAPER/10# LDPE/1# TIE-4# EVOH-1# TIE-5# PE SEALANT to introduce a tie layer between the EVOH and the LDPE deposited on the paper. Similarly, the type of polyethylene in the polymeric layer can be different than the LDPE used in the sealant and the thickness of the LDPE layer can be independently adjusted to optimize product performance.
(25) Now with reference to
(26) The line 400 includes two sections. The first section forms a coated substrate including the paper or PET layer with the polymeric barrier layer coated there on. The second section then applies the EVOH coextrusion to the coated substrate.
(27) In the form shown, the first section of the line 400 prepares the substrate, which may be, for example, the paper or PET film substrate. The substrate is unrolled from a main substrate roll 402 and fed toward an extrusion coater 406 which coats the substrate with the polymeric barrier layer.
(28) On the way to the extrusion laminator 406, the substrate from the main substrate roll 402 is fed past a treater 404 such as a flame treater or a corona treater that treats the surface of the substrate from the main substrate roll 402 such that the polymeric barrier layer created at the extrusion coater 406 will adhere well to the substrate. A liquid primer might also be applied to treat the surface. Although treatment of the substrate is depicted, it should be appreciated that such treatment is not required and some substrate materials may not need treatment prior to application of the polymeric barrier layer.
(29) At the extrusion coater 406, the substrate is fed through a nip point at which point the polymeric barrier layer is applied on the substrate as a melt curtain. The nip point occurs between a rubber nip roll 408 and a chill roll 410. As the substrate approaches the nip point, at a location above the nip point, a die 412 supplies a molten resin A (which may be, for example, low density polyethylene or any of the polymeric barrier materials listed above) as a melt curtain. This molten resin A is applied to a top surface of the substrate at the nip point, is cooled by the chill roll 410 to form a substrate/polymeric barrier layer structure, and then this coated substrate exits the extrusion coater 406.
(30) It should be appreciated that while the line 400 is shown including the extrusion coater 406 for the formation of the substrate/polymeric barrier layer structure, that if the coextrusion is to be directly applied to the paper that the extrusion coater station may be eliminated. Further, it is possible that the substrate could be coated by the polymeric barrier layer using methods other than an extrusion coater. For example, a spray coating could be applied to the paper or PET substrate.
(31) In any event, the substrate may be optionally fed past a treater 414 that treats the surface of the substrate for better adhesion to the coextrusion further down the line 400. Again, the treater 414 may incorporate a flame treatment, liquid priming, or a corona treatment to prepare the surface of the substrate.
(32) In the second portion of the line 400, a coextrusion coater 416 applies or coats the substrate with the EVOH coextrusion to form the packaging. In the coextrusion coater 416, the substrate is fed between a rubber nip roll 418 and a chill roll 420. A feedblock 422 of the coextruder 424 receives molten EVOH and at least one other molten resin B and/or C. If an EVOH-TSRB coextrusion is being formed, then the molten TSRB is also fed into the feedblock 422 (as B, with no C resin being fed) and a two layer coextrusion of EVOH-TSRB is extruded by the die 426 proximate the nip point such that the EVOH layer side contacts the paper substrate. In this form, the coextruder 424 may be only a two resin capable coextruder (i.e., the coextruder 424 does not need to be capable of receiving or extruding a molten resin C). If an EVOH-Tie-Sealant coextrusion is being formed, then in addition to the molten EVOH, the feedblock 422 receives both a molten tie resin (as B) and a molten sealant (as C) and the die 426 extrudes an EVOH-Tie-Sealant coextrusion such that the EVOH layer is applied to the substrate and laminated to the substrate at the nip point. After exiting the coextrusion coater 416, the packaging is wound up on a product wind-up roll 428.
(33) While specific embodiments of the present invention has been shown, various modifications falling within the breadth and scope of the invention will be apparent to one skilled in the art. Thus, the following claims should be looked to in order to understand the full scope of the invention.