LAYER SEQUENCE REPEATER MODULE FOR A MODULAR DISK CO-EXTRUSION DIE AND PRODUCTS THEREOF
A layer sequence repeater module for a co-extrusion die includes a cell formed of a plurality of thin annular disks stacked on top of each other in an axial direction of the co-extrusion die. Each disk includes a plurality of openings aligned with openings in the adjacent disks, thus forming multiple inner and outer melt passages. At least one of the layer sequence repeater module includes at least one first cap disk, at least one second cap disk, at least one distribution disk, at least one repeater disk and at least one spreader disk. The layer sequence repeater module may be a separately assembled and individually removable module of the co-extrusion die. Alternatively or additionally, the layer sequence repeater module may be incorporated into a module of the co-extrusion die.
This application is a divisional of U.S. patent application Ser. No. 13/752,458, filed Jan. 29, 2013 which in turn claims the benefit of and priority to U.S. Provisional Application No. 61/611,943, filed 16 Mar. 2012, the entirety of which applications are incorporated herein by reference.
FIELD OF INVENTIONThe present invention relates to a layer sequence repeater module for an annular die for extruding thermoplastic materials as well as products thereof More particularly, the present invention relates to an assembly of thin annular disks for an annular co-extrusion die and multi-layer products thereof.
BACKGROUND OF THE INVENTIONAnnular dies, such as, for example, co-extruded blown film dies, are used to form multi-layer products, e.g., blown films, from thermoplastic melts (hereinafter “melt”). Typically, modular co-extruded blown film dies include a module formed of an assembly of cells. Each cell usually includes several annular disks and produces one layer of a multi-layer product. Because each cell normally produces only one layer, conventional modular annular dies producing multi-layer products tend to become more bulky as more layers are added.
Co-extruded blown film dies have progressed to more and more layers over the past twenty years in order to combine diverse materials valued for performance enhancement or film properties in order to make unique specialty films. Most are now in the range of 7 to 11 layers. All vary in thickness capabilities but all may be termed as being able to make films containing micro-scale layers (hereinafter “micro-layer”).
Annular co-extruded films, tubing and parisons can vary in total thickness to the extent to which the melt is drawn from the die. The faster a melt is drawn the thinner it will be. Corresponding micro-layers within the total film thickness will be likewise proportionally affected in thickness by the draw. So the absolute thickness of any micro-layer is a moving target and may be best expressed in terms of relative thickness. Micro-layers within the standard co-extruded films usually may vary in relative thickness over a range from 1% to 100% of the total thickness. This limitation is related to total output rate of the film line and the maximum residence time of the melts within the die system before the polymer melt starts to degrade.
For example, layers within a typical 10-mil thick multi-layer product produced by conventional or modular annular dies are considered micro-layers, and typically range in thickness from about 0.1 mil to about 10 mils, and conventional and modular annular dies typically produce multi-layer products having anywhere from about 7 to 11 layers. Because cells that produce micro-layers in a modular annular die are relatively thick, increasing the number of micro-layers in a multi-layer product typically undesirably increases the overall thickness of the module containing these cells. Other conventional annular dies also have similar dimensional limitations.
There is an ongoing need for an improved modular annular die for producing multi-layer products with more, thinner layers. There is an ongoing need for multi-layer products having a higher number of layers that produce synergistic material responses such as mimicking the properties of blends without the incompatibility issues generally associated with blends. There is also a need to have films with very thin nano-layer bundles dispersed within a matrix of micro-layers so that the synergistic behavior of multiple materials in nano-layer form is not shackled by loss of high strength seal performance. Finally, there is an ongoing need for multi-layer products having many layers squeezed into the thickness or height dimensions that characterize most annular co-extrusion dies.
SUMMARY OF THE INVENTIONThe present invention is directed to a layer sequence repeater module for an annular co-extrusion die. The layer sequence repeater module of the present invention includes an assembly of thin annular disks, including at least one first cap disk, at least one distribution disk, at least one second cap disk, at least one repeater disk and at least one spreader disk. Desirably, the layer sequence repeater module of this invention includes one or more of each of the above-listed disks, depending on need. In a preferred embodiment of this invention, the entire layer sequence repeater module and/or any component disk thereof is disposable and individually replaceable.
The layer sequence repeater module of this invention can be incorporated into an existing module of an annular co-extrusion die, or, alternatively or additionally, can be a separately assembled and removable component within an annular co-extrusion die.
In one embodiment, the layer sequence repeater module includes a forward distribution section at the entry end of the layer sequence repeater module, and a reverse distribution section at the exit end of the layer sequence repeater module. Each distribution section includes a distribution disk sandwiched between a first cap disk and a second cap disk. Each distribution section distributes one melt and directs the flow of the distributed melt to inner passages and/or openings of repeater disk(s) and spreader disk(s) of the layer sequence repeater module, whereby each melt is formed into one or more layers. The forward distribution section directs the flow of the melt it distributes in a forward direction. The forward direction within the layer sequence repeater module extends from the entry end to the exit end thereof. The reverse distribution section directs the flow of the melt it distributes in a reverse direction. The reverse direction within the layer sequence repeater module extends from the exit end to the entry end thereof. Thus, in at least one embodiment of the layer sequence repeater module according to this invention, two or more melts flow in opposite directions.
The layer sequence repeater module may include additional distribution sections, each distributing at least one additional melt. Each additional distribution section may be a forward distribution section or a reverse distribution section, as described above. In one embodiment of this invention, the layer sequence repeater module only includes one or more forward distribution sections and no reverse distribution section. In another embodiment of this invention, the layer sequence repeater module only includes one or more reverse distribution sections and no forward distribution section.
The layer sequence repeater module further includes one or more repeater disks and one or more spreader disks. The repeater disk(s) and spreader disk(s) are alternately positioned within the layer sequence repeater module and receive distributed melts from one or more distribution sections and/or distributed disks. In one embodiment of the layer sequence repeater module including a forward distribution section and a reverse distribution section, the spreader disks and repeater disks are preferably positioned between the two distribution sections.
In operation, one or more melts are fed into one or more entry openings of the first cap disk. From the first cap disk, melts are directed to the remaining disks of the layer sequence repeater module. Specifically, melts may be directed to one or more distribution disks. Each distribution disk distributes one melt and directs the distributed melt from a plurality of distribution outlet openings of the distribution disk into a corresponding plurality of inner flow openings of a second cap disk and/or a plurality of inner passages of a repeater disk. After distribution, each melt flows in corresponding selections, respectively, of inner passages of repeater disks and inner openings of spreader disks. Specifically, each repeater disk has a plurality of inner passages, including one or more selections of inner passages, where each selection of inner passages accommodates one melt. In one embodiment, a selection of inner passages includes eight inner passages. Similarly, each spreader disk has a plurality of inner openings, including one or more selections of inner openings, where each selection of inner openings accommodates one melt. In one embodiment, a selection of inner openings includes eight inner openings. Desirably, one or more selections of inner passages correspond with one or more selections of inner openings, such as to provide a continuous flow path for each melt within the layer sequence repeater module. Each spreader disk further includes a flow region connected to a first selection of inner openings. The melt received by the first selection of inner openings of the spreader disk is desirably formed into a layer. The spreader disk forms a layer from a desired melt by positioning the spreader disk such that the first selection of inner openings receive the flow of the desired melt. Spreader disks desirably alternate with repeater disks such that every other disk is a spreader disk.
Because the spreader disks and repeater disks desirably alternate within the layer sequence repeater module, a layer can be formed by every other disk. Consequently, and because of the minimal thicknesses of the disks, the layer sequence repeater module according to the present invention lends itself to producing multiple-layer products with a die that is much less massive than conventional dies.
As the number of layers within a co-extruded film product increases and the corresponding layer thickness decreases, film property changes may be seen. For example, films can be made in the order of 25 layers where every other layer was an elastomer. The film properties become closer to a physical blend of the two materials without having the usual incompatibility issues such as optical haze or lowered physical properties to develop.
On the other hand, there are advantages to having one or more thicker layers strategically placed within very many thinner layers. An example would be to achieve a higher seal strength especially if the interlayer bond strength of the inner layers were weaker than the seal strength desired. Therefore, having both thicker and thinner layers within the same film structure can be extremely desirable.
In order to better identify thicker and thinner layers within the same film structure, there is a thickness term used herein to identify the thinner layers from the layer sequence repeater (LSR) module of the invention. Since the thickness of the thinner layers produced by the LSR module of this invention is at least about 10% less than the thickness of a corresponding micro-layer, these layers are herein defined using the next smaller measurement unit. Hereinafter, the term “nano-layer” will be used to refer to the thinner layers formed by the LSR module of this invention. Nano-layers typically have thickness measured in nanometers, in the sub-micron range.
In general, nano-layers will appear within a film structure having micro-layers as the major materials and therefore are clearly recognized by the fact that they appear in bundles of nano-layers, each nano-layer being in the order of about 10% or more thinner than the surrounding micro-layers.
There is a region where the thickness of the nano-layers may approach that of some of the surrounding micro-layers. This is most likely to happen in the 1-10% thickness region that in the thicker layers. The overlap is an inevitable consequence of operating at the limits of die and material capability. However, the clearly identifiable feature of having nano-layer bundles dispersed amongst micro-layers is a unique and identifiable feature of nano-layers produced by an LSR module.
The LSR module will be shown to produce many layers in a designed sequence that is joined in a parallel flow arrangement where each material is permitted to flow in a slower more natural fashion without undue stress developing. Because the melt flow undergoes less manipulation, the quality of the layers produced is very high and similar to the surrounding micro-layers. The annular nature of the LSR module also distinguishes it from the layer multiplier. Films blown from annular dies tend to have more balanced properties than films drawn from flat dies.
The layer sequence repeater module of the present invention produces nano-scale layers (hereinafter “nano-layer”) that are at least about 10% thinner, and can be an order of magnitude thinner than micro-scale layers produced by conventional modular dies.
Other advantages will be apparent to those skilled in the art from the following detailed description taken in conjunction with the drawings.
Those skilled in the art and following the teachings herein provided will appreciate that while the descriptions below of various layer sequence repeater modules of this invention include preferred configurations, such configurations are used for illustrative purposes only and may be modified as appropriate, depending on need.
The present invention relates to a layer sequence repeater module for an extrusion and/or a co-extrusion die. The layer sequence repeater module includes at least one cell that includes a plurality of axially disposed thin annular disks. The layer sequence repeater module can be used in a co-extrusion die to extrude or co-extrude resin materials to form multi-layer products, such as, for example, blown films containing nano-layers. The layer sequence repeater module of this invention used in a modular disk die may also be used to create a co-extruded tube, such as a hose, a co-extruded rod formed from multiple continuous layers of material to create a generally solid rod structure, or parison (a generally elliptical uninflated tube used in blow molding). The present invention is also directed to multi-layer products, especially those containing nano-layers, produced by the layer sequence repeater module and dies incorporating one or more layer sequence repeater modules of this invention.
The layer sequence repeater module of the present invention may be used in a modular disk co-extrusion device, such as the co-extrusion die disclosed in U.S. Pat. No. 5,762,971, issued 9 Jun. 1998, U.S. Pat. No. 6,000,926, issued 14 Dec. 1999, and/or U.S. Pat. No. 6,413,595, issued 2 Jul. 2002. The above-listed U.S. patents are hereby incorporated by reference herein in their entirety and are made a part hereof, including but not limited to those portions which specifically appear hereinafter.
The layer sequence repeater module of the present invention can be a module of a co-extrusion die. For example, one or more layer sequence repeater modules of this invention may be incorporated into any of the modules disclosed in the above-referenced U.S. patents. Alternatively or additionally, one or more layer sequence repeater modules of the present invention can be employed as separately assembled and removable components of a multi-component-module within a co-extrusion die. For example, with reference to U.S. Pat. No. 5,762,971, the layer sequence repeater module of this invention may be formed as one or more co-extrusion dies cells, or may be employed as a separately assembled and removable component positionable between two adjacent cells, or may be insertable into one or more of cells. A co-extrusion die may include one or more layer sequence repeater modules according to this invention.
The layer sequence repeater module of the invention will now be described in greater detail. Referring to
The term “nano-layer” as used throughout this specification means a layer of extruded material, the thickness of which is at least about 10% less than the thickness of a micro-layer, suitably at least about 50% less than the thickness of a micro-layer, and can be an order of magnitude (at least about 90% less) than the thickness of a micro-layer. Micro-layers typically have the thicknesses measured in micrometers or microns. The thickness of a micro-layer may range from about 1-1000 microns, suitably about 10-500 microns, or about 25-250 microns. Nano-layers typically have thicknesses measured in nanometers. The thickness of a nano-layer is typically less than one micron (1000 nanometers) and may range from about 1-1000 nanometers, suitably about 10-900 nanometers, or about 20-800 nanometers. Micro-layers 44 and nano-layers 46 are illustrated in
As illustrated in
The thin annular disks that form the layer sequence repeater module 30 of this invention will now be described in greater detail.
The term “opening”, “channel” or “passage” as used throughout this specification means an opening, a channel or a passage, respectively, extending in an axial direction of the thin annular disk through the entire thickness of the disk.
The first cap disk 32 includes at least two entry openings 33 disposed along or with respect to a circumference 35 of the first cap disk 32. In one embodiment, as shown in
For illustration purposes, the design of the layer sequence repeater module 30 shown in
One or more entry openings 33 of the first cap disk 32 may be replaced with a termination point. A termination point terminates the flow of a melt within the layer sequence repeater module at the termination point and prevents the melt to flow to the next disk, if any. A termination point preferably is a physical barrier and/or the lack of an opening. The first cap disk 32 shown in
In one embodiment, for example as shown in
The axial alignment of the distribution inlet opening 54, 54a with respect to the entry openings 33a, 33b or 33c of the first cap disk 32 determines the resin stream that is distributed by the distribution disk 36. For example, referring to
The distribution disk 36 illustrated in
In certain embodiments of this invention, for example as shown in
In one embodiment (
In operation, the second cap disk 34 may direct a distributed melt, e.g., stream b, to the next disk via the inner flow openings 65. Alternatively, the second cap disk 34 may direct stream b to the next disk via an outer flow opening 64, which may be aligned with distribution inlet opening 54 of the distribution disk 36. Alternatively, second cap disk 34 may terminate the flow of stream b by having a termination point 31 aligned with distribution inlet opening 54 of the distribution disk 36. A termination point 31 will terminate the resin passage of stream b such that the flow of stream b will stop at the second cap disk 34. For example, as shown in
Referring to
The plurality of inner passage openings 68 includes at least one selection of inner passage openings and preferably a plurality of selections of inner passage openings. Each selection of inner passage openings preferably accommodates a different melt stream. In one embodiment of this invention, the plurality of inner passage openings includes two selections of inner passage openings, such as a first selection of inner passage openings 68a and a second selection of inner passage openings 68b, as shown in
The repeater disk 40 may include one or more termination points 31 replacing one or more outer passage openings 66. The repeater disk 40 shown in
Each repeater disk 40 may have an axial thickness (not shown) of less than about 0.1 inches, preferably less than about 0.07 inches, and most preferably, less than about 0.05 inches. In one embodiment of this invention, one or more repeater disks 40 have an axial thickness of about 0.033 inches.
The spreader disk 38 includes at least one and preferably a plurality of outer openings 70 radially disposed along a circumference 74 of the spreader disk 38. The one or more outer openings 70 are axially aligned with one or more respective outer passage openings 66 of repeater disk 40, outer flow openings 64 of second cap disk 34, outer distributor openings 62 and/or distribution inlet opening 54 of the distribution disk 36 and/or entry openings 33 of the first cap disk 32. The spreader disk 38 additionally includes a plurality of inner openings 71, including a plurality of selections of inner openings. For example, in one embodiment, the spreader disk 38 includes two selections of inner openings 71, such as a first selection of inner openings 71 a and a second selection of inner openings 71b shown in
Referring to
Each spreader disk 38 may have an axial thickness (not shown) of less than about 0.1 inches, more preferably less than about 0.05 inches, and most preferably less than about 0.02 inches. In one embodiment of this invention, one or more spreader disks 38 have an axial thickness of about 0.016 inches.
The inclusion of repeater disks 40 in one or more cells of the layer sequence repeater module enables what was previously a single melt stream forming a single layer, to be divided into multiple smaller melt streams forming multiple thinner layers in the product. Without the repeater disks, a single cell would typically be capable of forming only a single layer, and would typically include a first cap disk 32, a distribution disk 36, a second cap disk 34, a spreader disk 38, and a third cap disk 32, similar to the arrangement described in U.S. Pat. No. 5,762,971. In order to make a film having multiple layers, multiple cells (each including a similar arrangement of disks) would be stacked together. The inclusion of repeater disks 40 enables multiple layers to be formed from a single cell, and allows the layers to be thinner. As shown in
The disks described above are arranged to form the layer sequence repeater module 30 of the present invention. One possible arrangement of disks is shown in
In one embodiment, the layer sequence repeater module 30 includes a plurality of thin annular disks arranged as shown in
The layer sequence repeater module 30 of this invention may include any number of spreader disks 38 alternating with repeater disks 40, depending on need. For example, if a seven nano-layer product is desired, the layer sequence repeater module 30 may include seven spreader disks 38, alternating with repeater disks 40. If a twenty-one nano-layer product is desired, the layer sequence repeater module 30 may include twenty-one spreader disks 38, alternating with repeater disks 40.
The layer sequence repeater module 30 of this invention may include one or more distribution sections 73 and/or distribution disks 36, depending on need. For example, in order to make a multi-layer product from two melts, the layer sequence repeater module 30 will desirably include two distribution sections 73 or, alternatively, two distribution disks 36. In order to make a multi-layer product from three melts, the layer sequence repeater module 30 will desirably include three distribution sections 73 or, alternatively, three distribution disks 36. In order to make a multi-layer product from four or more melts, the layer sequence repeater module will desirably have the corresponding number of distribution sections 73 and/or distribution disks 36. Alternatively, one or more melts may be distributed within the annular die before entering the layer sequence repeater module 30.
As briefly described above, the layer sequence repeater module 30 may have one or more distribution sections 73. Each distribution section 73 includes a distribution disk 36. In one embodiment, the distribution section 73, such as the distribution section 73x shown in
Distribution sections 73x and 73z shown in
Another embodiment of the layer sequence repeater module 30 is shown in
The first distribution section 73x shown in.
The layer sequence repeater module 30 shown in
The disks making up the layer sequence repeater module 30 can be made of any material suitable for use in a co-extrusion die. Suitable materials include, for example, ceramic, plastic or metallic materials that can withstand a welded attachment or the clamping pressure of the securing means and that do not chemically or thermally react with the melts being processed. Preferably the disks comprise a material that facilitates easy and inexpensive manufacture of the disks themselves. A preferred disk may comprise, for example, metallic materials such as steel and aluminum. More preferably, each disk has smooth surfaces so that a surface from a disk intimately abuts a surface from an axially adjacent disk. Such intimate contact will ensure that melt streams flowing through the layer sequence repeater module are properly directed and without leaking. Where poor surface quality disks are being used it is preferable that the disks are secured together by glue or welds to reduce leaking.
The disks in the layer sequence layer repeater module can be secured by disk bolts (not shown). These bolts can be inserted in a plurality of unused melt holes such as those aligned with inlet openings, if available. Alternatively, dedicated holes (not shown) in each disk specifically made for the disk bolts can also be provided. However, these dedicated holes are preferably placed such that the disk bolts would not interfere with the melt flow, for example, in the channels in the distribution disk 36 or the flow region of the spreader disk. Also, other securing means, such as for example, glue, may be used. Each disk can be glued to the axially adjacent disks within the layer sequence repeater module. Any glue material suitable for securing the material making up the disks may be used so long as the processed melt streams do not chemically react with the glued materials. An example of acceptable glue material for metallic disks including steel and aluminum (specifically product number DK-175-022A), is an inorganic polymer ceramic glaze from Cerdec Corporation of Washington, Pa.
In one embodiment of this invention, certain disks or sets of disks within the layer sequence repeater may be permanently joined together. One such means of permanently joining disks within the layer sequence repeater together is with spot welds between abutting surfaces of adjacent disks. Specifically, a spreader disk and a repeater disk, or a repeater disk and two spreader disks on either side of the repeater disk may be connected with respect to each other with spot welds.
Other means of welding known to those having ordinary skill in the art, such as braze welding, may be used to join two or more disks within a cell. A preferred weld would render grinding disk surfaces smooth following placement of the weld.
In yet another preferred embodiment, certain disks or a group of two or more disks can be machined from a single piece of material. Like a welded group of disks, a single-piece machined cell creates a permanent connection among groups of disks.
The layer sequence repeater module can be used to produce multilayer films having large numbers of thin layers and superior orientation properties. The superior orientation is believed to result because the thin layers are gently aligned in the melt phase, with very little stress in the alignment. Each and every nanolayer surface is formed separately between two metal die surfaces separated by a minimal gap before the slow moving melt joins the common melt path within the annulus of the die. Overall, there is more melt surface to polymer contact throughout a melt cross section leaving a modular disk die with a layer sequence repeater module, than in a conventional die. Also each nanolayer generated has a high ratio of surface area to thickness. This condition requires a gentle, low stress melt alignment to avoid breakage in the individual nanolayers.
The gentle, low stress melt flow through the layer sequence repeater module is enabled by the fact that the melt flows through the layers in parallel, instead of in series. For example, an internal die gap for each nanolayer may be set at 0.017 inch (431 microns). To produce a 25-layer film from two polymers, the layer sequence repeater module would have 25 of these gaps, 13 for the first polymer and 13 for the second polymer. This means that each polymer would have an equivalent die gap exceeding 0.2 inch (12.5 mm), specifically 0.017 inch (431 microns)×13 for the first polymer and 0.017 inch (431 microns)×12 for the second polymer. This is very large compared to the normal 0.030-0.060 inch (762-1524 microns) die gap for a single film layer in a conventional die. Thus, compared to a conventional die, the polymer flow through the layer sequence repeater module is comparatively slow and gentle, due to the parallel flow arrangement. The flow remains parallel until all of the layers are joined together at the central opening 49 defined by the inner radius 48 of the thin annular disks.
The gentle, low stress melt flow through the layer sequence repeater module results in a gentle alignment of molecules. This allows for greater stretching during subsequent uniaxial or biaxial orientation because more alignment and stretching of molecules occurs during the stretching process than would typically be the case with films made from conventional extrusion processes. The greater stretching during orientation can result in improved properties, such as tensile strength and puncture resistance. The nanolayer films also exhibit improved thermoforming, because thermoforming and orientation require similar stretching processes.
Various conventional processes can be used to orient the multilayer films prepared using the layer sequence repeater module, to obtain nanolayer oriented films. The quickest way is to stretch orient the film as it is being blown and is cooling. This generally creates oriented shrink films with low shrink force.
A double bubble process can also be used. A first blown film bubble is produced, then cooled and quenched, then reheated and stretched in a trapped air second bubble. This process involves colder biaxial stretching that results in higher shrink force and higher tensile strength films.
A tenter frame process can also be used to heat and stretch the film. The multilayer film can be blown, collapsed and slit to form flat tape. The flat tape is then heated and stretched (uniaxially or biaxially) using the tenter frame.
Other advantages and characteristics of the present invention are illustrated in the following examples.
EXAMPLESA layer sequence repeater module was assembled and inserted into an annular die, as shown in
A 2-inch die and a four-extruder downward co-extrusion line were utilized.
Extruders A and D had a 1.25-inch diameter, and 22:1 L/D steel screws with a chopper mixing tip and a breaker plate and a compression ratio of 3:1. Extruder A was driven by a 3 HP AC Vari-drive.
Two satellite ¾-inch extruders B and C were on a common drive with extruder A. Extruders B and C delivered resin at about a total of 40% of extruder A. Extruders B and C had a ¾-inch diameter, and 28:1 L/D steel screws with a chopper mixing tip and no breaker plate and a compression ratio of 3:1.
The expected layer thickness values are summarized below with extruder A delivering at 40 rpm, extruders B and C each delivering at 20% of extruder A, and extruder D delivering at 30 rpm or 20% of A×30/40.
Each of layers a (2 total layers a)=10×20/62=3.23 mil (82 microns)
Each of layers d (2 total layers d)=10×3/62=0.48 mil (12.2 microns)
Each of layers c (11 total layers c)=0.73/62=0.012 mil (305 nanometers)
Each of layers b (10 total layers b)=0.8/62=0.012 mil (305 microns)
Thick tubing was drawn slowly from the die and set aside to cool. The thick tubing was then cut with a hacksaw and shaved with a razor. Under a 10 times magnifier, about ⅓ of the thickness of the tubing consisted of two micro-layers formed from materials a and d, another ⅓ of the thickness of the tubing consisted of twenty-one nano-layers, and the final ⅓ of the thickness of the tubing consisted again of two micro-layers formed from materials d and a. The product samples are shown in
With reference to Tables 2-7 below, references to Materials A-J are made to the following Resins A-J, respectively:
- Resin A=Dow 6411, a low density polyethylene of about 2 MI obtained from Dow Plastics;
- Resin B=Topas® 8007, a cyclic olefin copolymer (COC) available from Polyplastics Co., Ltd.;
- Resin C=Rexene® 204 (E4.5% VA 2MI) obtained from Rexene Corporation;
- Resin D=DOW LDPE 4012, a low density polyethylene of about 10 MI available from Dow Plastics;
- Resin E=Vistamaxx™ 6100, a propylene-ethylene polymer available from ExxonMobil Chemical Company
- Resin F=Milliken® 3276 HPP, a clarified test resin obtained from Milliken Chemical;
- Resin G=Clyrell RC 1314, a polypropylene random copolymer available from LyondellBassell Industries;
- Resin H=960 HDPE Pactiv, a high density polyethylene of about 5 MI, obtained from Pactiv Corporation;
- Resin I=EVAL® L171B, an ethylene vinyl alcohol (EVOH) available from Eval Company of America; and
- Resin J=ADMER® NF498A, a polyethylene adhesive resin available from Mitsui Chemicals America, Inc.
Samples were prepared under extrusion conditions summarized in Table 2 below.
Samples 7-1 and 7-2 had the following structure: Resin A/Resin A/Resin B/Resin A/ . . . (alternating Resins A and B) . . . /Resin A/Resin B/Resin A/Resin A. A thick 10 mil tubing was prepared to clearly see the nano-layers in a cross section. Slight melt instability was observed.
Sample 7-5 was prepared to determine if resin viscosity changes would improve the thick film quality. The output of extruder A was increased to 40 rpm to make 15 mil tubing. Sample 7-5 had the following structure: Resin C/Resin C/Resin B/Resin C . . . (alternating Resins B and C) . . . Resin C/Resin B/Resin C/Resin C. It was observed that substituting a 10 MI resin with a 2 MI resin increased melt instability.
Sample 7-6 had the following structure: Resin C/Resin C/Resin B/Resin A . . . (alternating Resins A and B) . . . Resin A/Resin B/Resin C/Resin C. It was observed that by adding the 10 MI resin back into the twenty-one nano-layer layer sequence repeater improved the film quality. However, some melt instability was still present.
Sample 7-7 had the following structure: Resin A/Resin A/Resin B/Resin A . . . (alternating Resins A and B) . . . Resin A/Resin B/Resin A/Resin A. It was observed that the quality of film was very good and slightly better as compared with sample 7-1. However, traces of melt instability were still observed.
Sample 7-8 had the following structure: Resin A/Resin A/Resin B/Resin D/ . . . (alternating Resins B and D) . . . /Resin D/Resin B/Resin A/Resin A. It was observed that the quality of sample 7-8 was worse than sample 7-7.
Sample 7-9 had the same structure as samples 7-1 and 7-7, but the melt delivery temperature of Resin B was raised. It was observed that raising the melt delivery temperature of Resin B improved the film quality further with only the slightest traces of melt instability.
Example 2Samples were prepared under extrusion conditions summarized in Table 3 below.
Further samples were prepared under extrusion conditions summarized in Table 4 below.
The run started with the initial extrusion conditions shown in the first column of Table 3 above and then immediately progressed to the next set of extrusion conditions shown in the second column of Table 3 above. Resin B was used in extruder B. A sample of a very thick melt was collected and shaven with a razor in order to see the twenty-one nano-layers. The nano-layers were visible under a 10 times magnifier and occupied about ⅓ of the total structure. Samples 7-10 and 7-11 were collected.
The speed of the pinch rolls was increased to a setting of 100, and sample 7-12 was collected. The speed of the pinch rolls was reduced to a setting of 70, and sample 7-13 was collected. The speed of the pinch rolls was further reduced to a setting of 50, and sample 7-14 was collected. It was observed that all samples were of good quality. Resin E was then fed to extruder D, and sample 7-15 was collected. Again it was observed that the film quality was good.
Next, polypropylene (PP) was added to extruder A. With reference to Table 4, the first resin tried was Resin F. Severe melt instability was observed, and sample 7-16 was collected. The second resin tried was Resin G in extruder A. Although melt stability generally improved, some melt instability was still observed. Sample 7-17 was collected. The third resin tried was Resin H in extruder C. It was observed that the resulting melt was a much better quality melt. Samples 7-18 and 7-19 were collected.
With reference to Examples 1 and 2, it was found that Resin A and H co-extruded with Resin B were the only polyethylene melts relatively free from melt instability. Resin G used with Resin E as the adhesive resulted in good melt stability.
Example 3Samples were prepared under extrusion conditions summarized in Table 5 below.
The run started with oven dried Resin I in extruder B, Resin A in extruder A, Resin J in extruder C and Resin E in extruder D. Good melt stability was observed, and films ranging in thickness were produced and collected. Film thicknesses ranged from 6 mil in sample 8-1 to 1 mil in sample 8-7.
Example 4Samples were prepared under extrusion conditions summarized in Table 6 below.
Clarified polypropylene (PP) was used in extruder A. Resin E was used in extruder D to act as an adhesive layer on both sides of the twenty-one nano-layer structure of alternating layers of Resin J and Resin I. Samples 8-8 through 8-11 were collected. Throughout the collection of samples 8-8 through 8-11, portions of the film showed melt instability regardless of the conditions as shown in Table 6 above. The melt instability disappeared as Resin I was flushed with Resin A from extruder B, indicating that the viscosity of Resin I should be made similar to the viscosity of Resin A in order to produce quality films from these materials. Birefringence from the light was observed on the side of the film having some melt instability. Clear film samples had a special sparkle also probably due to birefringence.
Example 5Samples were prepared under extrusion conditions summarized in Table 7 below.
Thick 12-15 mil EVOH tubing was made. Samples 8-13 through 8-17 were all very similar.
With reference to Examples 3-5, films of excellent co-extrusion stability having the following structure: polyethylene (PE)/Resin E/Resin J/Resin I . . . (alternating Resins I and J) . . . Resin I/Resin J/Resin E/polyethylene (PE) were blown into films ranging in thickness from 5 mil to 1 mil. PE was then replaced with clarified PP to make clear films. Some melt instability was observed on one side of the bubble. The melt instability disappeared when Resin I was replaced with Resin A. A 12-15 mil film, similar to the first sample, was made in the final run. Birefringence was observed on the bubble with reflected light. The clear films had a brilliant sparkle to them. Since melt instability subsided when Resin A replaced Resin I, an EVOH with a melt viscosity similar to Resin A should make a better quality clear film.
Therefore, the layer sequence repeater module and/or a die including the layer sequence repeater module of the present invention has the ability to produce coextruded multi-layer products containing large numbers of layers (e.g. 21, 25, 51 and more) as well as products made up of large number of different materials. In one embodiment of this invention, a plurality of nano-layers are sandwiched between two or more micro-layers. The micro-layers may provide support and stability to the otherwise very thin nano-layers. The multi-layer products can be made of any melt material that can be extruded. Suitable materials include, for example, polyethylene (“PE”), polypropylene (“PP”), ethylene vinyl acetate (“EVA”), ethylene vinyl alcohol (“EVOH”), cyclic olefin copolymers (“COC”), and/or other thermoplastic materials as well as elastomer materials such as, for example, copolymers of alkenes having from 2 to about 30 carbons in the alkyl chain.
Additional Film StructuresThe use of ethylene vinyl alcohol (“EVOH”) to make thin nanolayer barrier films has led to the identification of a new crystal form of EVOH that is more deformable and has higher energy associated with it. The more deformable crystal structure has proven to be highly stretchable at a temperature just above its glass transition temperature (Tg) at 60° C. For example, EVOH in conventional barrier films can be about 0.3 mils (7.6 microns) thick. In a 25-layer nanofilm using EVOH for 12 of the layers, the same amount of EVOH can be split into layers having equal thickness of 635 nanometers. In another example, the total number of layers is increased to 77, with 38 of them being EVOH, and the film is stretch oriented to a total thickness of 0.026 mil (660 nm). In this example, the total amount of EVOH can be split into layers having equal thickness of 8.6 nanometers (with all 77 layers having the same thickness). A polyamide resin or a polyolefin-based adhesive can be used to form the remaining layers of the EVOH barrier film, and the entire nanolayer structure can be encapsulated between two outer layers of suitable polyethylene or other olefin polymer.
The following film structures have been produced using the layer sequence repeater module, and can be produced with or without variations.
Structure AFilm structure A, an oriented barrier film, includes a first outer layer of polyethylene, followed by a first tie (adhesive) layer, followed by 25 alternating layers of Nylon 6 (13 layers) and EVOH (12 layers), followed by a second tie layer and a second outer polyethylene layer. One or both outer polyethylene layers can be formed of a sealant material, such as a linear low density polyethylene or an ethylene vinyl acetate copolymer. The 25 nanolayers were produced as described above, using the layer sequence repeater module, with oriented layer thicknesses of 635 nm. The remaining layers were produced using conventional cells as described above with respect to
Film structure B, an oriented non-barrier microlayer shrink film, includes six layers of a first polyethylene, followed by thirteen alternating layers of second and third polyethylenes, followed by six additional layers of the first polyethylene, for a total of 25 layers. All 25 layers were microlayers produced using the layer sequence repeater module. Various types of polyethylene can be employed, including materials such as linear low density polyethylene and ethylene vinyl acetate, especially for the outer layers. As explained above, the formation of microlayers in the layer sequence repeater module involves a gentler melt flow which brings the layers together under less stress. The resulting multilayer film has improved orientation and shrink properties compared to conventional shrink films having fewer and thicker layers.
Structure CFilm structure C is a vanation of Structure A, with a larger number of polyethylene microlayers and additional barrier layers on both sides of the nanolayer barrier bundle. Structure C, an oriented barrier film, includes an eight microlayer alternating sequence of polyethylene and adhesive (repeated four times), followed by a two-layer sequence of Nylon 6/66 and EVOH, followed by the 25 nanolayer sequence of Nylon 6 (13 layers) alternating with EVOH (12 layers), followed by an additional two-layer sequence of EVOH and Nylon 6/66, followed by an additional eight microlayer alternating sequence of adhesive and polyethylene (repeated four times). The first and second eight-layer sequences of polyethylene/adhesive can utilize the same or different polyethylenes and the same or different adhesive resins. The two-layer sequences of Nylon 6/66 and EVOH can be nanolayers or microlayers. The Film structure C can be made using one or more layer sequence repeater modules stacked together, or can be made with a middle layer sequence repeater module equipped for 25 layers, sandwiched between two modular disk coextrusion die modules, each equipped for 8 layers.
Structure DFilm structure D is an all nanolayer non-barrier oriented shrink film including 26 alternating layers of a second polyethylene (13 layers) and a first polyethylene (13 layers), followed by 25 alternating layers of the second polyethylene (13 layers) and the first polyethylene (12 layers), followed by 26 alternating layers of the first polyethylene (13 layers) and the second polyethylene (13 layers), for a total of 77 alternating polyethylene layers. The film structure can be made by stacking three layer sequence repeater module together, each equipped to produce 25 or 26 alternating layers. Various polyethylene resins (including without limitation linear low density polyethylene and ethylene vinyl acetate copolymers) can be used for optimal performance.
Additional Die StructuresThe layer sequence repeater module can also be used to assemble additional, more complex coextrusion die structures, including the nanolayer-producing die structures illustrated in
Module 130 is a layer sequence repeater module similar to module 120, except that the sequence of repeater disks and spreader disks may be varied to produce a larger or smaller number of nanolayers, and the internal die gaps may vary according to the thickness of the individual disks. In the embodiment shown, for example, the sequence of repeater disks and spreader disks can be varied to produce 2 nanolayers, and the internal die gaps may again be 0.017 inc. Module 140 is another conventional modular disk coextrusion die module capable of producing a plurality of microlayers, for example six microlayers in the embodiment shown, or any desired number of microlayers. The internal die gaps may also vary according to the disk thickness, and may be 0.030 in the embodiment shown.
In order to produce barrier films using complex die 100, modules 110 and 140 can each be fed using two extruders to produce alternating layers of olefin polymer/tie layer, repeated three times. The olefin polymer layers can be polyethylene, polypropylene, linear low density polyethylene, or a sealing material such as ethylene vinyl acetate copolymer. The tie layers can be polyolefin-based adhesive, ethylene vinyl acetate copolymer, ionomer, or the like. Modules 120 and 130 can be used to produce alternating nanolayers of barrier materials such as alternating layers of polyamide/ethylene vinyl alcohol. Alternatively, the nanolayers can be alternating layers of polyamide/adhesive tie layer, or ethylene vinyl alcohol/adhesive tie layer, or any suitable barrier structure. The complex multilayer films thus produced can be uniaxially or biaxially oriented using any of the techniques described above.
Referring to
The embodiment of complex die 200 shown in
Of course, it should be understood that a wide range of changes and modifications can be made to the embodiments described above. It is therefore intended that the foregoing description illustrates rather than limits this invention, and that it is the following claims, including all equivalents, which define this invention.
Claims
1. A coextruded film comprising more than thirty layers;
- the thirty layers comprising twenty-one layers A and B in an alternating A/B sequence;
- each of the layers A comprising a first polymer composition;
- each of the layers B comprising a second polymer composition;
- wherein each of the layers A is a nanolayer having a thickness less than one micron.
2. The coextruded film of claim 1, wherein the second polymer composition is different than the first polymer composition.
3. The coextruded film of claim 1, wherein the second polymer composition is the same as the first polymer composition.
4. The coextruded film of claim 1, wherein each of the layers B is a nanolayer having a thickness less than one micron.
5. The coextruded film of claim 1, wherein each of the layers B is a micro-layer having a thickness of 1-1000 microns.
6. The coextruded film of claim 1, wherein each of the layers A has a thickness of 10-900 nanometers.
7. The coextruded film of claim 6, wherein each of the layers B has a thickness of 10-900 nanometers.
8. The coextruded film of claim 6, wherein each of the layers B has a thickness of 10-500 microns.
9. The coextruded film of claim 1, wherein one of the first and second polymer compositions comprises an elastomer.
10. The coextruded film of claim 1, wherein one of the first and second polymer compositions comprises ethylene vinyl alcohol and the other of the first and second polymer compositions comprises an adhesive.
11. The coextruded film of claim 1, wherein one of the first and second polymer compositions comprises a low density polyethylene and the other of the first and second polymer compositions comprises a cyclic olefin copolymer.
12. The coextruded film of claim 1, wherein one of the first and second polymer compositions comprises a cyclic copolymer and the other of the first and second polymer compositions comprises ethylene vinyl acetate.
13. The coextruded film of claim 1, wherein one of the first and second polymer compositions comprises ethylene vinyl alcohol and the other of the first and second polymer compositions comprises a polyethylene adhesive resin.
14. The coextruded film of claim 1, wherein one of the first and second polymer compositions comprises a polyamide and the other of the first and second polymer compositions comprises ethylene vinyl alcohol.
15. The coextruded film of claim 1, wherein one of the first and second polymer compositions comprises polyethylene and the other of the first and second polymer compositions comprises a different polyethylene.
16. The coextruded film of claim 1, comprising fifty-one layers.
17. The coextruded film of claim 1, comprising seventy-seven layers.
18. A coextruded film comprising twenty-five layers;
- the twenty-five layers comprising twenty-one layers A and B in an alternating A/B sequence;
- each of the layers A comprising a first polymer composition;
- each of the layers B comprising a second polymer composition;
- the twenty-five layers further comprising layers C and D on both sides of the twenty-one layers A and B in alternating A/B sequence;
- wherein each of the layers A, C and D is a nanolayer having a thickness of less than one micron.
19. The coextruded film of claim 18, wherein the second polymer composition is different from the first polymer composition.
20. The coextruded film of claim 18, wherein the second polymer composition is the same as the first polymer composition.
21. The coextruded film of claim 18 wherein each of the layers C and D comprises the first polymer composition.
22. The coextruded film of claim 18, wherein each of the layers C and D comprises a third polymer composition that is different from the first polymer composition.
23. The coextruded file of claim 18, comprising a plurality of layers C and D, wherein each of the layers C and D comprises a third polymer composition that is the same as the first or second polymer composition.
24. A coextruded film comprising a plurality of layer sets;
- each layer set comprising twenty-five layers, wherein the twenty-five layers comprise twenty-one layers A and B in an alternating sequence;
- each of the layers A comprising a first polymer composition;
- each of the layers B comprising a second polymer composition that is different from the first polymer composition;
- wherein each of the layers A is a nanolayer having a thickness less than one micron.
25. The coextruded film of claim 24, wherein the second polymer composition is different from the first polymer composition.
26. The coextruded film of claim 24, wherein the second polymer composition is the same as the first polymer composition.
27. The coextruded film of claim 24, comprising seventy-seven layers and including three of the layer sets.
28. The coextruded film of claim 1, wherein the film is an annular film.
29. The coextruded film of claim 1, wherein the film is an oriented shrink film.
30. The coextruded film of claim 1, wherein the film is a flat tape.
31. The coextruded film of claim 18, wherein the film is an annular film.
32. The coextruded film of claim 18, wherein the film is an oriented shrink film.
33. The coextruded film of claim 18, wherein the film is a flat tape.
34. The coextruded film of claim 24, wherein the film is an annular film.
35. The coextruded film of claim 24, wherein the film is an oriented shrink film.
36. The coextruded film of claim 24, wherein the film is a flat tape.
Type: Application
Filed: Oct 27, 2014
Publication Date: Apr 2, 2015
Inventor: Henry G. SCHIRMER (Spartanburg, SC)
Application Number: 14/524,861
International Classification: B32B 27/08 (20060101); B32B 27/30 (20060101); B32B 27/32 (20060101); B32B 7/02 (20060101);