Bag made from high-strength heat-shrinkable film exhibiting directional tear, and process utilizing same
10189621 ยท 2019-01-29
Assignee
Inventors
- Richard M. Dayrit (Simpsonville, SC)
- Robert A. Odabashian (Greer, SC, US)
- Janet W. Rivett (Simpsonville, SC, US)
- Thomas D. Kennedy (Simpsonville, SC, US)
- Diana Huerta (Moore, SC, US)
- Tom Bonner (Greer, SC, US)
- Rodney R. Hodgson (Greenville, SC, US)
- Mendy W. Mossbrook (Woodruff, SC, US)
- H. Walker Stockley (Spartanburg, SC)
Cpc classification
B65D75/5805
PERFORMING OPERATIONS; TRANSPORTING
Y02W30/80
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
B65D75/00
PERFORMING OPERATIONS; TRANSPORTING
B65D75/58
PERFORMING OPERATIONS; TRANSPORTING
Abstract
A heat-shrinkable bag has a means for initiating a manual tear that can be propagated to open the bag and allow a product to be readily removed therefrom, without the use of a knife or scissors or any other implement. The bag is made from a heat-shrinkable multilayer film having a Peak Load Impact Strength of at least 50 Newtons per mil. The means for initiating tearing results in a first tear in the first side of the bag, and a second tear in the second side of the bag. The first tear and the second tear are each capable of being manually propagated through a heat seal and across the bag, or down the length of the bag, with the tear being capable of being manually propagated through and to an opposite bag edge, so that the product inside a package can be readily removed from the bag. A process for making a package and manually opening the package, comprises placing a product inside the bag, sealing the bag closed, shrinking the film around the product, manually initiating and manually propagating the first and second tears, and readily removing the product from the bag.
Claims
1. A heat-shrinkable bag comprising a heat-shrinkable multilayer film having an inside seal layer heat sealed to itself at a heat seal, the bag further comprising a first side, a second side, an open top, and a bag skirt outward of the heat seal, the bag skirt comprising a bag edge and a first means for initiating tearing, the first means being in the first side of the bag, the bag skirt also comprising a second means for initiating tearing, the second means being in the second side of the bag, the bag being capable of having a manually-initiated, manually-propagated first tear in a machine direction in the first side of the bag, and a manually-initiated and manually-propagated second tear in the machine direction in the second side of the bag, the first tear and the second tear each being capable of being propagated in the machine direction from the respective first and second means for initiating tearing, with each tear being propagated through the heat seal and across the bag, or down the length of the bag, with the tears being capable of being manually propagated in the machine direction through and to an opposite bag edge, so that upon making a package by placing a product inside the bag, sealing the bag closed so that a package is formed, and shrinking the film around the product, the resulting package can be manually opened, and the product readily removed from the bag, by manually initiating tears in the machine direction from the first and second means for initiating tearing, with the tears being manually propagated in the machine direction through the seal and to the opposite bag edge, and wherein the multilayer film exhibits a Peak Load Impact Strength, determined using ASTM D 3763-95A, of at least 50 Newtons per mil, wherein the bag further comprises a means for assisting grip of the multilayer film, wherein the means for assisting grip comprises a partial hole cut having a hanging chad therein, and wherein the heat-shrinkable bag does not comprise a patch thereon, and wherein at least one layer of the multilayer film comprises an incompatible polymer blend selected from the group consisting of: (A) a blend of ethylene/alpha-olefin copolymer with ethylene/vinyl acetate; (B) a blend of ionomer resin with ethylene/vinyl acetate copolymer, and/or polybutylene, and/or polypropylene; (C) a blend of homogeneous ethylene/alpha-olefin copolymer with recycled polymer blend comprising ethylene homopolymer, propylene homopolymer, ethylene copolymer, propylene copolymer, polyamide, ethylene/vinyl alcohol copolymer, ionomer resin, anhydride-modified ethylene/alpha-olefin copolymer, and antiblock; (D) a blend of ethylene/vinyl acetate copolymer with polypropylene, and/or polybutylene, and/or modified ethylene/vinyl acetate copolymer, and/or polystyrene; (E) a blend of ethylene/alpha-olefin copolymer with polypropylene and/or polybutylene; (F) a blend of single site catalyzed polypropylene with homogeneous ethylene/alphaolefin copolymer and/or ethylene/vinyl acetate; (G) a blend of polypropylene and/or ethylene/propylene copolymer and/or polybutylene with ethylene/methyl acrylate copolymer and/or ethylene/acrylic acid copolymer and/or ethylene/butyl acrylate copolymer; and (H) a blend of polyamide with polystyrene and/or ethylene/alpha-olefin copolymer and/or ethylene/vinyl acetate copolymer and/or styrene/butadiene copolymer.
2. The heat-shrinkable bag according to claim 1, wherein the bag is a lay-flat, end-seal bag made from a seamless tubing, the end-seal bag having an open top, first and second folded side edges, and an end seal across a bottom of the bag, with the first and second means for initiating tearing being in the bag skirt that is outward of the end seal, with the first tear being a machine-direction tear of the film, and the second tear being a machine-direction tear of the film, with each tear being capable of being manually propagated down the length of the end-seal bag to the opposite edge of the end-seal bag.
3. The heat-shrinkable bag according to claim 1, wherein the bag is a lay-flat, side-seal bag made from a seamless tubing, the side-seal bag having an open top, a folded bottom edge, and first and second side seals with respective first and second bag skirts outward of respective first and second side seals, with the first and second means for initiating tearing being in the first bag skirt and outward of the first side seal, with the first tear being a machine-direction tear and the second tear being a machine-direction tear, with each tear being capable of being manually propagated across the full width of the side-seal bag to the opposite edge of the side-seal bag.
4. The heat-shrinkable bag according to claim 1, wherein the multilayer film exhibits a Peak Load Impact Strength, determined using ASTM D 3763-95A, of from 50 to 250 Newtons per mil, and the multilayer film has a total thickness, before shrinking, of from 1.5 mils to 5 mils.
5. The heat-shrinkable bag according to claim 1, wherein the first means for initiating tearing is overlapping or coincident with the second means for initiating tearing, with the bag further comprising a third means for initiating tearing and a fourth means for initiating tearing that is overlapping or coincident with the third means for initiating tearing, with the first and second means for initiating tearing being positioned in a bag skirt for making a manual tear in a machine direction, and the third and fourth means for initiating tearing being positioned for making a manual tear in a transverse direction.
6. The heat-shrinkable bag according to claim 1, wherein upon making a package by placing a product inside the bag, evacuating the atmosphere from the bag, sealing the bag closed so that a package is formed, and shrinking the film around the product, the resulting package can be manually opened, and the product readily removed from the bag, by manually initiating tears from the first and second means for initiating tearing.
7. The heat-shrinkable bag according to claim 1, wherein at least one layer of the multilayer film comprises a polymer having a Young's modulus of at least 80,000 psi.
8. The heat-shrinkable bag according to claim 1, wherein at least one layer of the multilayer film comprises an inorganic filler.
9. The heat-shrinkable bag according to claim 8, wherein the filler comprises at least one member selected from the group consisting of silicate, silica, silicone resin, zinc sulfide, wollastonite, microsphere, glass fiber, metal oxide, calcium carbonate, sulfate, aluminum trihydrate, feldspar, perlite, gypsum, iron, fluoropolymer, crosslinked polymethylmethacrylate, talc, diatomaceous earth, zeolite, mica, kaolin, carbon black, and graphite.
10. The heat-shrinkable bag according to claim 2, wherein the first means for initiating tearing overlaps the second means for initiating tearing when the bag is in the lay-flat configuration.
11. The heat-shrinkable bag according to claim 2, wherein the first means for initiating tearing coincides with the second means for initiating tearing when the bag is in the lay-flat configuration.
12. The heat-shrinkable bag according to claim 1, wherein the multilayer film has a total free shrink at 185 F. of from 10 percent to 150 percent, measured using ASTM D-2732.
13. The heat-shrinkable bag according to claim 1, wherein the multilayer film comprises a barrier layer containing at least one member selected from the group consisting of polyvinylidene chloride, saponified ethylene/vinyl acetate copolymer, amorphous polyamide, polyamide MXD6, polyester, and polyacrylonitrile.
14. The heat-shrinkable bag according to claim 1, wherein the multilayer film comprises: (A) a first layer that is an outer food-contact layer and that also serves as a seal layer, the first layer comprising homogeneous ethylene/alpha-olefin copolymer; (B) a second layer comprising ethylene/methyl acrylate copolymer; (C) a third layer comprising a blend of polyamide 6 with polyamide 6I,6T; (D) a fourth layer comprising EVOH; (E) a fifth layer comprising a blend of polyamide 6 with polyamide 6I,6T; (F) a sixth layer comprising ethylene/methyl acrylate copolymer; and (G) a seventh layer comprising a blend of low density polyethylene and linear low density polyethylene; and wherein the layers are present in the order of first/second/third/fourth/fifth/sixth/seventh.
15. The heat-shrinkable bag according to claim 1, wherein the multilayer film comprises: (A) a first layer that is an outer food-contact layer and that also serves as a seal layer, the first layer comprising a blend of ethylene/vinyl acetate copolymer, linear low density polyethylene, and homogeneous ethylene/alpha-olefin copolymer; (B) a second layer comprising polyvinylidene chloride; (C) a third layer that comprises a blend of ethylene/vinyl acetate copolymer, linear low density polyethylene, and homogeneous ethylene/alpha-olefin copolymer; and wherein the layers are present in the order of first/second/third.
16. The heat-shrinkable bag according to claim 1, wherein the multilayer film comprises: (A) a first layer that is an outer food-contact layer and that also serves as a seal layer, the first layer comprising a blend of homogeneous ethylene/alpha-olefin copolymer and linear low density polyethylene; (B) a second layer comprising a blend of heterogeneous ethylene/alpha-olefin copolymer and ethylene/vinyl acetate copolymer; (C) a third layer comprising ethylene/vinyl acetate copolymer; (D) a fourth layer comprising polyvinylidene chloride; (E) a fifth layer comprising ethylene/vinyl acetate copolymer; (F) a sixth layer comprising a blend of heterogeneous ethylene/alpha-olefin copolymer and ethylene/vinyl acetate copolymer; and (G) a seventh layer comprising a blend of homogeneous ethylene/alpha-olefin copolymer and linear low density polyethylene; and wherein the layers are present in the order of first/second/third/fourth/fifth/sixth/seventh.
17. The heat-shrinkable bag according to claim 1, wherein the blend of incompatible polymers comprises at least one blend selected from the group consisting of: (A) a blend of ethylene/alpha-olefin copolymer with ethylene/vinyl acetate copolymer; (B) a blend of ionomer resin with ethylene/vinyl acetate copolymer, and/or polybutylene, and/or polypropylene; (C) a blend of ethylene/vinyl acetate copolymer with polypropylene, and/or polybutylene, and/or modified ethylene/vinyl acetate copolymer; (D) a blend of ethylene/alpha-olefin copolymer with polypropylene and/or polybutylene; (E) a blend of single site catalyzed polypropylene with homogeneous ethylene/alphaolefin copolymer and/or ethylene/vinyl acetate; (F) a blend of polypropylene and/or ethylene/propylene copolymer and/or polybutylene with ethylene/methyl acrylate copolymer and/or ethylene/acrylic acid copolymer and/or ethylene/butyl acrylate copolymer; and (G) a blend of polyamide with ethylene/alpha-olefin copolymer and/or ethylene/vinyl acetate copolymer.
18. The heat-shrinkable bag according to claim 1, wherein the first tear and the second tear are each being capable of being propagated in the machine direction.
19. The heat-shrinkable bag according to claim 1, wherein the bag further comprises first and second grip assist means on a first lay-flat side of the bag, and third and fourth grip assist means on the second lay-flat side of the bag, and a first means for tear initiation on the first lay-flat side of the bag between the first and second grip assist means, and a second means for tear initiation on the second lay-flat side of the bag between the third and fourth grip assist means.
20. The heat-shrinkable bag according to claim 19, wherein the first and third grip assist means are coincident and the second and fourth grip assist means are coincident and the first and second means for tear initiation are coincident.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION
(36) As used herein, the term film is inclusive of plastic web, regardless of whether it is film or sheet. The film can have a total thickness of 0.25 mm or less, or a thickness of from 1.5 mils to 10 mils, or from 1.5 to 5 mils, or from 1.8 mils to 4 mils, or from 2 mils to 3 mils.
(37) The multilayer, heat-shrinkable film from which the bag is made exhibits a Peak Load Impact Strength, determined using ASTM D 3763-95A, of at least 50 Newtons per mil. ASTM D 3763-95A is hereby incorporated, in its entirety, by reference thereto. The heat-shrinkable film can have a Peak Load Impact Strength, determined using ASTM 3763-95A, of from 50 to 250 Newtons per mil, or from 60 to 200 Newtons per mil, or from 70 to 170 Newtons per mil; or from 80 to 150 Newtons per mil; or from 85 to 140 Newtons per mil; or from 95 to 135 Newtons per mil.
(38) As used herein, the phrase machine direction refers to the direction in which the film emerges from the die. Of course, this direction corresponds with the direction the extrudate is forwarded during the film production process. The phrase machine direction corresponds with longitudinal direction. Machine direction and longitudinal direction are abbreviated as MD and LD, respectfully.
(39) However, as used herein, the phrase machine direction includes not only the direction along a film that corresponds with the direction the film traveled as it passed over idler rollers in the film production process, it also includes directions that deviate up to 44 degrees from the direction the film traveled as it passed over idler rollers in the production process.
(40) As used herein, the phrase transverse direction refers to a direction perpendicular to the machine direction. Transverse direction is abbreviated as TD. The transverse direction also includes directions that deviate up to 44 degrees from the direction the film traveled as it passed over idler rollers in the production process.
(41) As used herein, the term bag refers to a packaging article having an open top, side edges, and a bottom edge. The term bag encompasses lay-flat bags, pouches, casings (seamless casings and backseamed casings, including lap-sealed casings, fin-sealed casings, and butt-sealed backseamed casings having backseaming tape thereon). Various casing configurations are disclosed in U.S. Pat. No. 6,764,729 B2, to Ramesh et al, entitled Backseamed Casing and Packaged Product Incorporating Same, which is hereby incorporated in its entirety, by reference thereto.
(42) The term bag also includes that portion of a package that is derived from a bag. That is, once a product is placed inside a bag, the bag is sealed closed so that it surrounds the product. Excess bag length (i.e., the bag tail) can optionally be cut off along a line close to the seal made across the bag to enclose the product within the bag, and thereafter optionally the film can be shrunk around the product. The portion of the bag that remains and is configured around the product is herein also within the term bag. The phrase an opposite bag edge refers to the edge of the bag that is directly across from the bag edge having the means for initiating tear. For example, a bag top edge is opposite the bag bottom edge; a first bag side edge is opposite the second bag side edge. As used herein, the phrase a side of the bag is used with reference to each of the first and second sides of a lay-flat bag, as well as each of the two principal, flat sides of a gusseted bag.
(43) As used herein, the phrase bag skirt refers to that portion of a bag that is outward of a heat seal, i.e., the excess bag length or width on the non-product side of the heat seal. In an end-seal bag, the bag skirt is short in the machine direction and long in the transverse direction. In a side-seal bag, the bag skirt is long in the machine direction and short in the transverse direction. In either case, the width of the bag skirt is the shorter dimension of the skirt, and the length of the bag skirt is the longer dimension of the skirt. A bag skirt can have a width, before the film is shrunk, of at least 5 millimeters, or at least 10 millimeters, or at least 15 millimeters, or at least 20 millimeters, or at least 25 millimeters, or at least 30 millimeters. The bag skirt can have a width of from 5 to 100 millimeters, or from 10 to 50 millimeters, or from 15 to 40 millimeters, or from 20 to 35 millimeters.
(44) As used herein, the phrase lay-flat bag refers generically to non-gusseted bags used for the packaging of a variety of products, particularly food products. More specifically, the phrase lay-flat bag includes side seal bag, end-seal bag, L-seal bag, U-seal bag (also referred to as a pouch), and backseamed bag (also referred to as T-seal bag). The backseam can be a fin seal, a lap seal, or a butt-seal with a backseaming tape. Before the bag is shrunk, it can have a length-to-width ratio of from 1:1 to 20:1; or from 1.5:1 to 8:1; or from 1.8:1 to 6:1; or from 2:1 to 4:1.
(45) The means for initiating tear can be a cut in the bag skirt. As used herein, the term cut refers to the penetration through the film, or shearing through the film, with a shearing means or edged instrument. The term cut is inclusive of both slits and notches. As used herein, the term slit refers to a cut through the film without the separation and removal of a piece of film from the bag. A slit can be from the edge of the bag (i.e., an edge slit) or internal, i.e., not extending to an edge (i.e., internal slit also referred to as a slit hole). The slit can be straight or curved or wavy.
(46) The term hole, as used herein, includes both an internal puncture (i.e., internal hole) or internal cut (i.e., an internal slit) through the packaging article, as well as an internal cut that removes a piece of film from the article. The hole can utilize a straight cut or a curved cut. The hole can be round or square or rectangular or irregular in shape.
(47) A notch is formed by a cut that removes a piece of film along an otherwise straight or smooth curved edge of a bag skirt or a bag tail, producing a point for stress concentration during the subsequent manual application of tearing force. A notch can be V-shaped or round or square or rectangular or oval or of any regular or irregular profile.
(48) The slit or notch or hole in the bag skirt can extend across at least 10 percent of the width of the bag skirt before the bag is shrunk; or at least 20 percent, or at least 30 percent or at least 40 percent, or at least 50 percent, or at least 60 percent, or at least 70 percent, or at least 80 percent, or at least 90 percent, of the width of the bag skirt or bag tail. The slit or notch or hole can angle inward, toward the bag center.
(49) In end-seal and side-seal bags, a portion of a bag skirt is in a first lay-flat side of the bag, and a portion of the same bag skirt is in a second lay-flat side of the bag. The first lay-flat side of the bag skirt can have a first means for initiating tearing, and the second lay-flat side of the bag can have a second means for initiating tearing.
(50) The first means for initiating tearing can overlap the second means for initiating tearing when the end-seal or side-seal bag (or any other bag) is in its lay-flat configuration, as well as in the shrunken package. Overlapping enhances the ease of simultaneously initiating and propagating the tears in the first and second sides of the bags. Moreover, the first means for initiating tearing can coincide (i.e., be positioned directly over and correspond with in length and shape) with the second means for initiating tearing when the bag is in its lay-flat configuration.
(51) The bag can be provided with both a first means for initiating tearing that is overlapping or coincident with the second means for initiating tearing, with the bag further comprising a third means for initiating tearing and a fourth means for initiating tearing, the fourth means for initiating tearing being overlapping or coincident with the third means for initiating tearing. The first and second means for initiating tearing can be positioned in a bag skirt for making a manual tear in a machine direction, with the third and fourth means for initiating tearing being positioned for making a manual tear in a transverse direction. The third and fourth means for initiating tearing can be positioned in a bag skirt, or near the top edge of the bag so that they are positioned in the bag tail after the product is placed in the bag and the bag sealed closed so that it surrounds the product.
(52) As used herein, the verb to tear refers to pulling an object apart by force. The noun tear refers to the resulting break in the object being torn. The tearing of the film results from placing the film under enough tension that it is pulled apart by the force. The pulling force is concentrated by the means for initiating tearing, which allows a smaller pulling force to pull the film apart, i.e., tear the film. The high impact strength heat-shrinkable films are not susceptible to being manually torn without the presence of the means for initiating tearing. In the heat-shrinkable bag, the high impact strength multilayer film undergoes tearing from the means for initiating tearing toward the opposite edge of the bag.
(53) The phrase means for initiating tearing, as used herein, refers to any one or more of a variety of means that can be located in the bag skirt (and/or in the bag tail). The means for initiating tearing allows manual tearing force to be concentrated on a point or small region of the film(s), so that tear initiation and tear propagation can be produced manually. A slit in the bag skirt, as illustrated in
(54) As used herein, the phrase manual and the term manually are both used with reference to tearing with the hands alone i.e., without the need for a knife, scissors, or any other implement to assist with initiating or propagating tearing of the film. The term manual is used with respect to tear initiation, i.e., the manual starting of the tearing action, as well as with respect to tear propagation, i.e., the manual continuation (i.e., extension) of a tear that has been manually initiated.
(55) In addition to the means for initiating tear, the bag can be provided with means for gripping. The means for gripping can enhance the tearing of the shrunken bag. The means for gripping can be in one lay-flat side of the bag or in both lay-flat sides of the bag. The means for gripping can be a hole in the bag skirt (and/or in the bag tail), an extension of the bag skirt (and/or the bag tail), or a separate film tab fastened to the bag skirt (and/or the bag tail). The separate film tab can be made from a thermoplastic polymer, paper, or other material, and can be heat-shrinkable or non-heat-shrinkable. The multilayer, heat-shrinkable bag can be provided with the combination of a means for initiating tear and a means for enhancing gripping of the bag. For example, the bag skirt can have a slit as the means for initiating tear and a hole as the means for enhancing gripping. See
(56) With respect to the tearing of the film from which the bag is made, as used herein the phrase the tear is capable of being propagated . . . refers to the manner in which the film tends to propagate the tear when the bag is subjected to an ordinary manual opening thereof, i.e., the bag being gripped and ripped in the ordinary course of opening. The bag tends to exhibit linear tear. Usually, the tear is substantially in line with the machine direction or substantially in line with the transverse direction.
(57) If the tear is being made in the machine direction of the film, the tear may be within from 0 to 44 degrees of the actual machine direction of the film, i.e., so long as the tear can be propagated toward and to the opposite side edge of the bag; or the tear may be within from 0 to 20 degrees, or within from 0 to 15 degrees, or within from 1 to 20 degrees, or within from 0 to 10 degrees; or within from 0 to 5 degrees, or within from 0 to 2 degrees of the machine direction of the film. The same holds true of transverse direction tearing, i.e., the tear may be within from 0 to 44 degrees of the actual transverse direction of the film; or the tear may be within 0 to 20 degrees, or within 1 to 20 degrees, or within from 0 to 10 degrees; or within from 0 to 5 degrees, or within from 0 to 2 degrees of the transverse direction of the film.
(58) As used herein, the phrase readily removed is applied to the removal of a product from a packaging article surrounding or substantially surrounding the product. As used herein, the phrase readily removed refers to the manual removal of the product from within the confines of the packaging article without any further substantial amount of tearing, and without any substantial further permanent deformation of the film. As used herein, the phrase substantial tearing of the film refers to tearing greater than or equal to 2 millimeters in length. As used herein, the phrase substantial permanent deformation of the film refers to a permanent stretching of the film greater than or equal to 2 millimeters at any location on the film.
(59) As used herein, the phrases seal layer, sealing layer, heat seal layer, and sealant layer, refer to an outer film layer, or layers, involved in heat sealing the film to itself, another film layer of the same or another film, and/or another article which is not a film. Heat sealing can be performed in any one or more of a wide variety of manners, such as melt-bead sealing, thermal sealing, impulse sealing, ultrasonic sealing, hot air sealing, hot wire sealing, infrared radiation sealing, ultraviolet radiation sealing, electron beam sealing, etc.). A heat seal is usually a relatively narrow seal (e.g., 0.02 inch to 1 inch wide) across a film. One particular heat sealing means is a heat seal made using an impulse sealer, which uses a combination of heat and pressure to form the seal, with the heating means providing a brief pulse of heat while pressure is being applied to the film by a seal bar or seal wire, followed by rapid cooling.
(60) In some embodiments, the seal layer can comprise a polyolefin, particularly an ethylene/alpha-olefin copolymer. For example, the seal layer can contain a polyolefin having a density of from 0.88 g/cc to 0.917 g/cc, or from 0.90 g/cc to 0.917 g/cc. The polyolefin can be an ethylene/alpha-olefin copolymer. More particularly, the seal layer can comprise at least one member selected from the group consisting of very low density polyethylene and homogeneous ethylene/alpha-olefin copolymer. Very low density polyethylene is a species of heterogeneous ethylene/alpha-olefin copolymer. The heterogeneous ethylene/alpha-olefin (e.g., very low density polyethylene) can have a density of from 0.900 to 0.917 g/cm.sup.3, and the homogeneous ethylene/alpha-olefin copolymer can have a density of from 0.880 g/cm.sup.3 to 0.910 g/cm.sup.3, or from 0.880 g/cm.sup.3 to 0.917 g/cm.sup.3. The polyolefin can be an ionomer resin or an ethylene/alpha-olefin copolymer. Metallocene-catalyzed sealants with densities of 0.917 g/cm.sup.3 or less, as well as a very low density polyethylene having a density of 0.912 g/cm.sup.3, provided excellent optics. Plastomer-type metallocene sealants with densities less than 0.910 g/cm.sup.3 also provided excellent optics.
(61) As used herein, the term barrier, and the phrase barrier layer, as applied to films and/or film layers, are used with reference to the ability of a film or film layer to serve as a barrier to one or more gases. In the packaging art, oxygen (i.e., gaseous O.sub.2) barrier layers can comprise, for example, at least one member selected from the group consisting of hydrolyzed ethylene/vinyl acetate copolymer (designated by the abbreviations EVOH and HEVA, and also referred to as saponified ethylene/vinyl acetate copolymer and ethylene/vinyl alcohol copolymer), polyvinylidene chloride, amorphous polyamide, polyamide MXD6 (particularly MXD6/MXDI copolymer), polyester, polyacrylonitrile, etc., as known to those of skill in the art. In addition to the first and second layers, the heat-shrinkable film may further comprise at least one barrier layer.
(62) The heat-shrinkable film can exhibit O.sub.2-transmission rate of from 1 to 20 cc/m.sup.2 day atm at 23 C. and 100% relative humidity, or from 2 to 15 cc/m.sup.2 day atm at 23 C. and 100% relative humidity, or from 3 to 12 cc/m.sup.2 day atm at 23 C. and 100% relative humidity, or from 4 to 10 cc/m.sup.2 day atm at 23 C. and 100% relative humidity. Alternatively, the heat-shrinkable film can exhibit an O.sub.2-transmission rate of from 21 cc/m.sup.2 day atm to 15,000 cc/m.sup.2 day atm, or from 500 cc/m.sup.2 day atm to 10,000 cc/m.sup.2 day atm, or from 2000 cc/m.sup.2 day atm to 6,000 cc/m.sup.2 day atm.
(63) As used herein, the phrase tie layer refers to any internal layer having the primary purpose of adhering two layers to one another. Tie layers can comprise any polymer having a polar group grafted thereon. Such polymers adhere to both nonpolar polymers such as polyolefin, as well as polar polymers such as polyamide and ethylene/vinyl alcohol copolymer. Tie layers can comprise at least one member selected from the group consisting of polyolefin (particularly homogeneous ethylene/alpha-olefin copolymer), anhydride-modified polyolefin, ethylene/vinyl acetate copolymer, and anhydride-modified ethylene/vinyl acetate copolymer, ethylene/acrylic acid copolymer, and ethylene/methyl acrylate copolymer. Typical tie layer polymers comprise at least one member selected from the group consisting of anhydride modified linear low density polyethylene, anhydride modified low density polyethylene, anhydride modified polypropylene, anhydride modified methyl acrylate copolymer, anhydride modified butyl acrylate copolymer, homogeneous ethylene/alpha-olefin copolymer, and anhydride modified ethylene/vinyl acetate copolymer.
(64) As used herein, the phrases inner layer and internal layer refer to any layer, of a multilayer film, having both of its principal surfaces directly adhered to another layer of the film.
(65) As used herein, the phrase outer layer refers to any film layer having less than two of its principal surfaces directly adhered to another layer of the film. A multilayer film has two outer layers, each of which has a principal surface adhered to only one other layer of the multilayer film.
(66) As used herein, the term adhered is inclusive of films which are directly adhered to one another using a heat seal or other means, as well as films which are adhered to one another using an adhesive which is between the two films. This term is also inclusive of layers of a multilayer film, which layers are of course adhered to one another without an adhesive therebetween. The various layers of a multilayer film can be directly adhered to one another (i.e., no layers therebetween) or indirectly adhered to one another (i.e., one or more layers therebetween).
(67) As used herein, the term package refers to packaging materials configured around a product being packaged. As such, the term package includes both the packaging around the product, and the product itself, i.e., the combination of the packaging and the product(s) within the package.
(68) Once a multilayer film is heat sealed to itself or another member of the package being produced (i.e., is converted into a packaging article, e.g., a bag, pouch, or casing), one outer layer of the film is an inside layer of the packaging article and the other outer layer becomes the outside layer of the packaging article. The inside layer can be referred to as an inside heat seal/product contact layer, because this is the film layer that is sealed to itself or another article, and it is the film layer closest to the product, relative to the other layers of the film. The other outer layer can be referred to as the outside layer and/or as the outer abuse layer or outer skin layer, as it is the film layer furthest from the product, relative to the other layers of the multilayer film. Likewise, the outside surface of a packaging article (i.e., bag) is the surface away from the product being packaged within the bag.
(69) While the multilayer heat-shrinkable film can be sealed to itself to form an end-seal bag or other bag, optionally, a heat-shrinkable patch film can be adhered to the bag. The patch film can be heat-shrinkable, and can have a total free shrink at 185 F. of at least 35 percent, measured in accordance with ASTM D-2732. The bag film and the patch film can have a total free shrink at 185 F. that are within 50 percent of one another, or within 20 percent of one another, or with 10 percent of one another, or within 5 percent of one another, or within 2 percent of one another. The patch may or may not cover the heat seal. If the patch covers a heat seal, optionally the heat seal may be made through the patch. If the tear is to be made though the bag and through the patch, the patch should cover a heat seal, and the means for initiating tear should be through both the bag film and the patch film. The bag can have a curved seal and the patch can extend into and through the region of the curved seal and over and past the curved seal. If the bottom edge of the bag is curved, a bottom edge of the patch can also be curved. The patch bag can have any desired configuration of patch on bag as disclosed in any one or more of U.S. Pat. Nos. 4,755,403, 5,540,646, 5,545,419, 6,296,886, 6,383,537, 6,663,905, 6,790,468, each of which is hereby incorporated, in its entirety, by reference thereto.
(70) End-seal bags with curved heat seals, and end-seal patch bags with curved heat seals, can be designed for have manual tear initiation and manual directional tear propagation. While the end-seal may be curved, the bottom edge of the bag may be straight across the tubing, or may also be curved. A curved bottom heat seal and a straight across bag bottom edge leaves room at the bottom corners of the bag for providing the means for tear initiation, and also for a means to facilitate gripping of the bag for the tearing operation. Patch bags with curved end seals are disclosed in U.S. Pat. No. 6,270,819, to Wiese, which is hereby incorporated, in its entirety, by reference thereto.
(71) The term polymer, as used herein, is inclusive of homopolymer, copolymer, terpolymer, etc. Copolymer includes copolymer, terpolymer, etc.
(72) Blends of incompatible polymers in one or more film layers can enhance the tear initiation, tear propagation, and linear tear properties of the film, including the ability to manually tear down the full length or across the full width of a package made from a bag which in turn has been made from film, i.e., tearing through a seal and through and to the opposite edge of the bag used to make the package. For a package made from an end-seal bag, the tear can be initiated in the bag skirt, and the tear can be manually extended for up to the full length of the package, i.e., to that portion of the package that corresponds with the opposite edge of the bag after the bag is used to make the package. For a package made from a side-seal bag, the tear can be initiated in the bag skirt, and the tear can be manually extended across the full width of the package (i.e., corresponding with the full machine direction dimension of the bag) for up to the full width of the package, i.e., to that portion of the package that corresponds with the opposite edge of the side-seal bag after the bag is used to make the package.
(73) As used herein, the phrase incompatible polymers refers to two polymers (i.e., a blend of at least two polymers) that are incapable of forming a solution or even a stable two-phase blend, and that tend to separate after being mixed. When blended, incompatible polymers are not miscible with one another, and phase separate into a continuous domain and a discontinuous domain that may be finely dispersed. The presence of one or more film layers comprising a blend of incompatible polymers may assist, enhance, or even cause the linear tear property of the multilayer heat-shrinkable film used to make the heat-shrinkable bag.
(74) The blend of incompatible polymers can comprise at least one blend selected from the group consisting of: (A) a blend of ethylene/alpha-olefin copolymer with ethylene/vinyl acetate copolymer (particularly EVA with at least 10 wt. % vinyl acetate, or at least 15 wt. % vinyl acetate, or at least 20 wt % vinyl acetate, or at least 25 wt. % vinyl acetate); (B) a blend of ionomer resin with ethylene/vinyl acetate copolymer, and/or polybutylene, and/or polypropylene (particularly propylene copolymer); (C) a blend of homogeneous ethylene/alpha-olefin copolymer with recycled polymer blend comprising ethylene homopolymer, propylene homopolymer, ethylene copolymer, propylene copolymer, polyamide, ethylene/vinyl alcohol copolymer, ionomer resin, anhydride-modified ethylene/alpha-olefin copolymer, and/or antiblock; (D) a blend of ethylene/vinyl acetate copolymer with polypropylene (particularly propylene/ethylene copolymer), and/or polybutylene, and/or modified ethylene/vinyl acetate copolymer, and/or polystyrene (particularly random and/or block styrene/butadiene copolymer); (E) a blend of ethylene/norbornene copolymer with ethylene/vinyl acetate copolymer and/or polypropylene and/or polybutylene; (F) a blend of ethylene/alpha-olefin copolymer with polypropylene (particularly propylene/ethylene copolymer) and/or polybutylene and/or ethylene/norbornene; (G) a blend of single site catalyzed polypropylene (i.e., homogeneous polypropylene) with homogeneous ethylene/alpha-olefin copolymer and/or ethylene/vinyl acetate; (H) a blend of polypropylene and/or ethylene/propylene copolymer and/or polybutylene with ethylene/methyl acrylate copolymer and/or ethylene/acrylic acid copolymer and/or ethylene/butyl acrylate copolymer; and (I) a blend of polyamide with polystyrene and/or ethylene/alpha-olefin copolymer and/or ethylene/vinyl acetate copolymer and/or styrene/butadiene copolymer (random and/or block copolymer).
(75) Several specific blends of incompatible polymers that may be used include the following: (i) a blend of 50 weight percent cyclic olefin copolymer with 50 weight percent propylene homopolymer; (ii) a blend of 70 wt. percent polystyrene with 30 wt. percent ethylene/vinyl acetate copolymer having a vinyl acetate content of 9 percent or 15 percent; (iii) a blend of 70 wt. percent very low density polyethylene and 30 wt. percent cyclic olefin copolymer; (iv) a blend of 70 weight percent ethylene/propylene copolymer and 30 weight percent homogeneous ethylene/alpha-olefin copolymer; (v) a blend of 70 weight percent ethylene/propylene copolymer and 30 wt. percent ethylene/vinyl acetate copolymer having a vinyl acetate content of 9 percent or 15 percent; (vi) a blend of 70 weight percent ethylene/propylene copolymer and 30 weight percent ethylene/methyl acrylate copolymer; (vii) a blend of 70 weight percent polystyrene with 30 weight percent amorphous nylon; (viii) a blend of 70 weight percent ionomer resin with 30 weight percent ethylene/vinyl acetate copolymer having a vinyl acetate content of 4 percent; (ix) a blend of 70 weight percent polyamide with 30 weight percent low density polyethylene; (x) a blend of 65 weight percent amorphous polyamide with 35% styrene/butadiene/styrene block copolymer.
(76) The tear initiation, tear propagation, and linear tear property of a multilayer heat-shrinkable film may also be enhanced by providing one or more layers of the film with a filler material, such as an inorganic filler. Polymeric systems that incorporate high filler concentrations may also enhance linear tear behavior. Depending on the particle size and dispersion, a filler concentration as low as 5 weight percent filler (i.e., based on total layer weight) in ethylene/alpha-olefin copolymer, polypropylene, propylene/ethylene copolymer, polybutylene, polystyrene/butadiene copolymer, ionomer resin, ethylene/vinyl acetate copolymer, ethylene/butyl acrylate copolymer, ethylene/methyl acrylate copolymer, ethylene/acrylic acid copolymer, polyester, polyamide, etc., may contribute to the linear tear behavior. More particularly, the presence of filler in an amount of from 5 to 95 weight percent, or in an amount of from 5 to 50 weight percent, or in an amount of from 10 to 40 weight percent, or from 20 to 35 weight percent, may be used.
(77) Suitable fillers include silicates (particularly sodium silicate, potassium silicate, and aluminum silicate, alkali alumino silicate), silica (particularly amorphous silica), siloxane, silicone resin, zinc sulfide, wollastonite, microspheres, glass fiber, metal oxide (particularly oxides of titanium, zinc, antimony, magnesium, iron, and aluminum), calcium carbonate, sulfate (particularly barium sulfate and calcium sulfate), aluminum trihydrate, feldspar, perlite, gypsum, iron, fluoropolymer, crosslinked polymethylmethacrylate, talc, diatomaceous earth, zeolites, mica, kaolin, carbon black, and graphite.
(78) The filler concentration required to achieve low tear initiation force is dependent on particle geometry, particle size, particle aspect ratio, and compatibility of the filler and the polymer matrix. Some fillers are chemically treated to improve the compatibility of the particle and the polymer into which it is dispersed.
(79) The tear initiation, tear propagation, and linear tear property of a multilayer heat-shrinkable film may also be enhanced by providing one or more layers of the film with a polymer that provides the film with a relatively high Young's modulus, e.g., a polymer having a Young's modulus of at least 80,000 psi. Such polymers can comprise at least one member selected from the group consisting of high density polyethylene, ultra high molecular weight polyethylene, polypropylene (particularly propylene homopolymer), styrene copolymer (particularly styrene/butadiene block copolymer), ethylene/norbornene copolymer, semi-crystalline polyamide, amorphous polyamide (including polyamide 6I/6T), polycarbonate, and polyester. The multilayer heat-shrinkable film may have a Young's Modulus of at least 80,000 psi. Young's modulus may be measured in accordance with one or more of the following ASTM procedures: D638, D882; D5026-95a; D4065-89, each of which is incorporated herein in its entirety by reference. The film may have a Young's modulus of at least about, and/or at most about, any of the following: 100,000; 130,000; 150,000; 200,000; 250,000; 300,000; 350,000; and 400,000 pounds/square inch, measured at a temperature of 73 F. The film may have any of the forgoing ranges of Young's modulus in at least one direction (e.g., in the machine direction or in the transverse direction) or in both directions (i.e., the machine (i.e., longitudinal) and the transverse directions).
(80) As used herein, terms such as polyamide, polyolefin, polyester, etc are inclusive of homopolymers of the genus, copolymers of the genus, terpolymers of the genus, etc, as well as graft polymers of the genus and substituted polymers of the genus (e.g., polymers of the genus having substituent groups thereon).
(81) As used herein, the phrase propylene/ethylene copolymer refers to a copolymer of propylene and ethylene wherein the propylene mer content is greater than the ethylene mer content. Propylene/ethylene copolymer is not a species of ethylene/alpha-olefin copolymer.
(82) The phrase ethylene/alpha-olefin copolymer is particularly directed to heterogeneous copolymers such as linear low density polyethylene (LLDPE), very low and ultra low density polyethylene (VLDPE and ULDPE), as well as homogeneous polymers such as metallocene catalyzed polymers such as EXACT resins obtainable from the Exxon Chemical Company, and TAFMER resins obtainable from the Mitsui Petrochemical Corporation. All these latter copolymers include copolymers of ethylene with one or more comonomers selected from C.sub.4 to C.sub.10 alpha-olefin such as butene-1 (i.e., 1-butene), hexene-1, octene-1, etc. in which the molecules of the copolymers comprise long chains with relatively few side chain branches or cross-linked structures. This molecular structure is to be contrasted with conventional low or medium density polyethylenes which are more highly branched than their respective counterparts. The heterogeneous ethylene/alpha-olefins commonly known as LLDPE have a density usually in the range of from about 0.91 grams per cubic centimeter to about 0.94 grams per cubic centimeter. Other ethylene/alpha-olefin copolymers, such as the long chain branched homogeneous ethylene/alpha-olefin copolymers available from the Dow Chemical Company, known as AFFINITY resins, are also included as another type of homogeneous ethylene/alpha-olefin copolymer useful in the film and process described herein.
(83) As used herein, the phrase heterogeneous polymer refers to polymerization reaction products of relatively wide variation in molecular weight and relatively wide variation in composition distribution, i.e., typical polymers prepared, for example, using conventional Ziegler-Natta catalysts. Heterogeneous copolymers typically contain a relatively wide variety of chain lengths and comonomer percentages. Heterogeneous copolymers have a molecular weight distribution (Mw/Mn) of greater than 3.0.
(84) As used herein, the phrase homogeneous polymer refers to polymerization reaction products of relatively narrow molecular weight distribution and relatively narrow composition distribution. Homogeneous polymers are useful in various layers of the multilayer heat-shrinkable film. Homogeneous polymers are structurally different from heterogeneous polymers, in that homogeneous polymers exhibit a relatively even sequencing of comonomers within a chain, a mirroring of sequence distribution in all chains, and a similarity of length of all chains, i.e., a narrower molecular weight distribution. Furthermore, homogeneous polymers are typically prepared using metallocene, or other single-site type catalysis, rather than using Ziegler Natta catalysts. Homogeneous ethylene/alpha-olefin copolymer can have a Mw/Mn of 3.0.
(85) As used herein, the term polyamide refers to a polymer having amide linkages, more specifically synthetic polyamides, either aliphatic or aromatic, either in semi-crystalline or amorphous form. It is intended to refer to both polyamides and co-polyamides. The polyamides can be selected from nylon compounds approved for use in producing articles intended for use in processing, handling, and packaging food, including homopolymers, copolymers and mixtures of the nylon materials described in 21 C.F.R. 177.1500 et seq., which is incorporated herein by reference. Exemplary of such polyamides include nylon homopolymers and copolymers such as those selected from the group consisting of nylon 4,6 (poly(tetramethylene adipamide)), nylon 6 (polycaprolactam), nylon 6,6 (poly(hexamethylene adipamide)), nylon 6,9 (poly(hexamethylene nonanediamide)), nylon 6,10 (poly(hexamethylene sebacamide)), nylon 6,12 (poly(hexamethylene dodecanediamide)), nylon 6/12 (poly(caprolactam-co-laurallactam)), nylon 6,6/6 (poly(hexamethylene adipamide-co-caprolactam)), nylon 6/66 (poly(caprolactam-co-hexamethylene adipamide)), nylon 66/610 (e.g., manufactured by the condensation of mixtures of nylon 66 salts and nylon 610 salts), nylon 6/69 resins (e.g., manufactured by the condensation of epsilon-caprolactam, hexamethylenediamine and azelaic acid), nylon 11 (polyundecanolactam), nylon 12 (polyauryllactam), nylon MXD6, nylon MXDI, nylon 6I/6T, and copolymers or mixtures thereof. Unless otherwise indicated, the phrase semi-crystalline polyamide includes all polyamides that are not considered to be amorphous polyamides. All semi-crystalline polyamides have a determinable melting point.
(86) The film is a heat-shrinkable film. The film can be produced by carrying out only monoaxial orientation, or by carrying out biaxial orientation. As used herein, the phrase heat-shrinkable is used with reference to films which exhibit a total free shrink (i.e., the sum of the free shrink in both the machine and transverse directions) of at least 10% at 185 F., as measured by ASTM D 2732, which is hereby incorporated, in its entirety, by reference thereto. All films exhibiting a total free shrink of less than 10% at 185 F. are herein designated as being non-heat-shrinkable. The heat-shrinkable film multilayer film can have a total free shrink at 185 F. of from 10 percent to 150 percent, or from 15 percent to 120 percent, or from 20 percent to 100 percent, or from 30 percent to 80 percent, or from 35 percent to 60 percent, as measured by ASTM D 2732.
(87) Heat shrinkability can be achieved by carrying out orientation in the solid state (i.e., at a temperature below the glass transition temperature of the polymer). The total orientation factor employed (i.e., stretching in the transverse direction and drawing in the machine direction) can be any desired factor, such as at least 2, at least 3, at least 4, at least 5, at least 6, at least 7, at least 8, at least 9, at least 10, at least 16, or from 1.5 to 20, from 2 to 16, from 3 to 12, or from 4 to 9.
(88) In one embodiment, the film does not comprise a crosslinked polymer network. In another embodiment, the film comprises a crosslinked polymer network. Optionally, the film can be irradiated to induce crosslinking of polymer, particularly polyolefin in the film. The film can be subjected to irradiation using an energetic radiation treatment, such as corona discharge, plasma, flame, ultraviolet, X-ray, gamma ray, beta ray, and high energy electron treatment, which induce cross-linking between molecules of the irradiated material. The irradiation of polymeric films is disclosed in U.S. Pat. No. 4,064,296, to BORNSTEIN, et. al., which is hereby incorporated in its entirety, by reference thereto. BORNSTEIN, et. al. discloses the use of ionizing radiation for crosslinking polymer present in the film.
(89) Radiation dosages are referred to herein in terms of the radiation unit RAD, with one million RADS, also known as a megarad, being designated as MR, or, in terms of the radiation unit kiloGray (kGy), with 10 kiloGray representing 1 MR, as is known to those of skill in the art. A suitable radiation dosage of high energy electrons is in the range of up to about 16 to 166 kGy, more preferably about 30 to 90 kGy, and still more preferably, 30 to 50 kGy. Preferably, irradiation is carried out by an electron accelerator and the dosage level is determined by standard dosimetry processes. Other accelerators such as a van der Graaf or resonating transformer may be used. The radiation is not limited to electrons from an accelerator since any ionizing radiation may be used.
(90) The heat-shrinkable, multilayer film used to make the end-seal bag can be fully coextruded, or prepared using an extrusion-coating process. Optionally, an annular extrudate (herein also referred to as a tape) can be irradiated before the additional layers are extrusion coated onto the substrate tape. Irradiation produces a stronger polymer network by crosslinking the polymer chains. Extrusion-coating allows a portion of the final multilayer structure to be crosslinked by irradiation (and thereby strengthened), in combination with avoiding irradiation of, for example, a layer of polyvinylidene chloride applied to the substrate via extrusion coating. Irradiation of polyvinylidene chloride is undesirable because irradiation can cause degradation of polyvinylidene chloride. Extrusion coating and irradiation are disclosed in U.S. Pat. No. 4,278,738, to Brax et al, which is hereby incorporated, in its entirety, by reference thereto.
(91) In the multilayer, heat-shrinkable film, all of the film layers can be arranged symmetrically with respect to the polymeric composition of each film layer. In addition, all of the film layers can be arranged symmetrically with respect to both composition and thickness. In one embodiment, the seal layer is thicker than the second outer layer. The seal layer can have a thickness of from 110% to 300% of the thickness of the second outer layer, or from 150% to 250% of the thickness of the second outer layer.
(92) One heat-shrinkable multilayer film from which the bag can be made comprises seven layers in the order: 1/2/3/4/5/6/7. The first layer is an outer food-contact layer and seal layer, and comprises homogeneous ethylene/alpha-olefin copolymer. The second layer comprising ethylene/methyl acrylate copolymer. The third layer comprises a blend of polyamide 6 with polyamide 6I, 6T. The fourth layer comprises EVOH. The fifth layer comprises a blend of polyamide 6 with polyamide 6I, 6T. The sixth layer comprises ethylene/methyl acrylate copolymer. The seventh layer comprises a blend of low density polyethylene and linear low density polyethylene. See Example 16, below.
(93) Another heat-shrinkable multilayer film from which the bag can be made comprises three layers in the order: 1/2/3. The first layer is an outer food-contact layer that also serves as a seal layer. The first layer comprises a blend of ethylene/vinyl acetate copolymer, linear low density polyethylene, and homogeneous ethylene/alpha-olefin copolymer. The second layer comprising polyvinylidene chloride. The third layer comprises a blend of ethylene/vinyl acetate copolymer, linear low density polyethylene, and homogeneous ethylene/alpha-olefin copolymer. See Example 12, below.
(94) Another heat-shrinkable multilayer film from which the bag can be made comprises seven layers in the order: 1/2/3/4/5/6/7. The first layer that is an outer food-contact layer and that also serves as a seal layer. The first layer comprises a blend of homogeneous ethylene/alpha-olefin copolymer and linear low density polyethylene. The second layer comprises a blend of heterogeneous ethylene/alpha-olefin copolymer and ethylene/vinyl acetate copolymer. The third layer comprises ethylene/vinyl acetate copolymer. The fourth layer comprises polyvinylidene chloride. The fifth layer comprises ethylene/vinyl acetate copolymer. The sixth layer comprises a blend of heterogeneous ethylene/alpha-olefin copolymer and ethylene/vinyl acetate copolymer. The seventh layer comprises a blend of homogeneous ethylene/alpha-olefin copolymer and linear low density polyethylene. See Examples 1 and 2, below.
(95)
(96)
(97) Grip assist holes can be sized to allow a user's finger(s) to be inserted therethrough to assist in gripping the film. Grip assist holes work in conjunction with the means for tear initiation, by providing a secure manual grip of the bag in a location designed to assist in generating tear initiation force along a tear line emanating from the means for tear initiation.
(98) The grip assist hole in a first lay-flat side of the bag can overlap or coincide with the grip assist hole in a second lay-flat side of the bag. While grip assist holes can have any desired shape (e.g., round, rectangular, square, triangular, pentagonal, hexagonal, etc.), preferably the holes are round, or any corners on the holes are rounded, to reduce the presence of stress concentration points that could cause a tear to initiate from the grip assist hole, as an objective is to have the tear initiated from the means for initiating tearing, with the tear running to an opposite side edge of the bag.
(99) In one embodiment, the grip-assist holes can be made by cutting through both lay-flat sides of the bag to remove a piece of film to form the holes. However, this process is more difficult to carry out, and it produces small, loose pieces of film corresponding with the size of the cut hole. These pieces of film may lodge inside the bag and thereafter adhere to a food product placed in the bag, which of course is an undesirable result. In order to prevent the production of a small, loose pieces of film, a cut can be made in the film in a shape that corresponds with a partial hole cut, i.e., a cut through the film to make a portion of the hole, the cut not being complete so that a hole is formed. Such a cut leaves a hanging chad so that no separated small pieces of film are produced by the cut.
(100)
(101) Hanging chad 36 can be made so that it is connected to film 11 at a region oriented towards tear initiation cuts 20 and 21, as illustrated in
(102)
(103)
(104)
(105) In
(106) In
(107) In
(108) In
(109) In
(110) In
(111) In
(112) In
(113) In
(114) In
(115) In
(116) In
(117)
(118) It has been found that tear initiation can be generated with less force if the means for initiating tear is a slit angled relative to the bag side edge, i.e., into the bag, as illustrated in, for example
(119) A plurality of the heat-shrinkable end-seal bags of can be supplied individually in a container, or as a set of individual bags in shingled relationship on one or more tapes in accordance with U.S. Pat. No. 4,113,139, hereby incorporated, in its entirety, by reference thereto.
(120) Alternatively, a plurality of bags can be provided as a continuous strand of serrated bags, as illustrated in
(121)
(122)
(123) The combination of the straight tear line 73 and the curved bottom seal 71 in the strand of serrated bags illustrated in
(124)
(125) After cooling or quenching by water spray from cooling ring 126, tubing 124 is collapsed by pinch rolls 128, and is thereafter fed through irradiation vault 130 surrounded by shielding 132, where tubing 124 is irradiated with high energy electrons (i.e., ionizing radiation) from iron core transformer accelerator 134. Tubing 124 is guided through irradiation vault 130 on rolls 136. Preferably, tubing 124 is irradiated to a level of about 4.5 MR.
(126) After irradiation, irradiated tubing 138 is directed through nip rolls 140, following which tubing 138 is slightly inflated, resulting in trapped bubble 142. However, at trapped bubble 142, the tubing is not significantly drawn longitudinally, as the surface speed of nip rolls 144 are about the same speed as nip rolls 140. Furthermore, irradiated tubing 138 is inflated only enough to provide a substantially circular tubing without significant transverse orientation, i.e., without stretching.
(127) Slightly inflated, irradiated tubing 138 is passed through vacuum chamber 146, and thereafter forwarded through coating die 148. Second tubular film 150 is melt extruded from coating die 148 and coated onto slightly inflated, irradiated tube 138, to form two-ply tubular film 152. Second tubular film 150 preferably comprises an O.sub.2-barrier layer, which does not pass through the ionizing radiation. Further details of the above-described coating step are generally as set forth in U.S. Pat. No. 4,278,738, to BRAX et. Al., which is hereby incorporated by reference thereto, in its entirety.
(128) After irradiation and coating, two-ply tubing film 152 is wound up onto windup roll 154. Thereafter, windup roll 154 is removed and installed as unwind roll 156, on a second stage in the process of making the tubing film as ultimately desired. Two-ply tubular film 152, from unwind roll 156, is unwound and passed over guide roll 158, after which two-ply tubular film 152 passes into hot water bath tank 160 containing hot water 162. The now collapsed, irradiated, coated tubular film 152 is submersed in hot water 162 (having a temperature of about 210 F.) for a retention time of at least about 5 seconds, i.e., for a time period in order to bring the film up to the desired temperature for biaxial orientation. Thereafter, irradiated tubular film 152 is directed through nip rolls 164, and bubble 166 is blown, thereby transversely stretching tubular film 152. Furthermore, while being blown, i.e., transversely stretched, nip rolls 168 draw tubular film 152 in the longitudinal direction, as nip rolls 168 have a surface speed higher than the surface speed of nip rolls 164. As a result of the transverse stretching and longitudinal drawing, irradiated, coated biaxially-oriented blown tubing film 170 is produced, this blown tubing preferably having been both stretched in a ratio of from about 1:1.5-1:6, and drawn in a ratio of from about 1:1.5-1:6. More preferably, the stretching and drawing are each performed a ratio of from about 1:2-1:4. The result is a biaxial orientation of from about 1:2.25-1:36, more preferably, 1:4-1:16. While bubble 166 is maintained between pinch rolls 164 and 168, blown tubing film 170 is collapsed by rolls 172, and thereafter conveyed through nip rolls 168 and across guide roll 174, and then rolled onto wind-up roll 176. Idler roll 178 assures a good wind-up.
(129)
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(135)
(136)
Resins Utilized in the Examples
(137) Unless otherwise indicated, the following listing of resins identifies the various resins utilized in Examples 1-35 below.
(138) TABLE-US-00001 Generic Resin Name Melt {additional Density Index Resin code Tradename information} (g/cc) (dg/min) Supplier ION 1 Surlyn Zinc neutralized ethylene 0.940 14 DuPont 1702-1 methacrylic acid copolymer ION 2 Surlyn Zinc neutralized ethylene 0.950 1.55 DuPont 1650 SB methacrylic acid copolymer + slip additive SSPE 1 Affinity Homogeneous 0.900 6.0 Dow 1280G ethylene/alpha-olefin copolymer SSPE 2 Affinity PL Homogeneous 0.900 g/cc 6.0 Dow 1281G1 ethylene/octene copolymer SSPE3 Affinity PL Homogeneous 0.902 3.0 Dow 1850G ethylene/octene copolymer SSPE4 Affinity PF Homogeneous 0.8965 g/cc 1.6 Dow 1140G ethylene/octene copolymer SSPE5 DPF 1150.03 Homogeneous 0.901 0.9 Dow Ethylene/octene copolymer SSPE6 Exceed Homogeneous 0.918 4.5 Exxon 4518 PA Ethylene/hexene Mobil copolymer VLDPE 1 XUS Very low density 0.903 0.5 Dow 61520.15L polyethylene VLDPE 2 Attane 4203 Very low density 0.905 0.80 Dow polyethylene VLDPE 3 Rexell Very low density 0.915 6.6 Huntsman V3401 polyethylene VLDPE 4 ECD 364 VLDPE (ethylene/hexene 0.912 1.0 ExxonMobil copolymer) LLDPE 1 Dowlex Linear Low Density 0.920 1.0 Dow 2045.03 Polyethylene LLDPE 2 LL 3003.32 Heterogeneous 0.9175 3.2 Exxon Ethylene/hexene Mobil copolymer Ion&Eva&Pb Appel Blend of ionomer, EVA, 0.932 3.7 DuPont 72D799 and polybutylene EVA&PP Versify Blend of EVA and 0.89 3.0 Dow XUR-YM Polypropylene 2006268985 RECLAIM TO35B Recycled multilayer film Sealed containing wide variety Air Corp of polymers, including ionomer resin, ethylene homo- and co-polymers, propylene homo- and co- polymers, EVOH, polyamide, anhydride modified polymers, ionomer, antiblock, etc. PP1 Inspire 112 Propylene homopolymer 0.9 0.4 Dow PP2 Basell Pro- Propylene homopolymer 0.902 34 Basell Fax PH835 Polyolefins PP3 PP3155 Propylene homopolymer 0.900 36 Exxon Mobil PP4 Escorene PP Propylene homopolymer 0.900 36.0 Exxon 3445 Mobil PB PB8640M Butene homopolymer 0.908 1 Basell Polyolefins ssPP Eltex Propylene/ethylene 0.900 5.5 Ineos P KS 409 copolymer znPP Escorene Propylene/ethylene 0.902 6.00 Ineos PP9012E1 copolymer Et-Pr TER Vistalon Ethylene-propylene diene 0.870 1.5 Exxon 7800 terpolymer Mobil MA-LLD 1 Tymor Maleic anhydride 0.921 2.0 Rohm & 1228B modified polyethylene Haas {blended with linear low density polyethylene} MA-LLD 2 PX 3227 Maleic anhydride 0.913 1.7 Equistar modified polyethylene Division {blended with linear low of density polyethylene} Lyondell MA-LLD 3 PX3236 Maleic anhydride 0.922 2.00 Equistar modified polyethylene Division {blended with linear low of density polyethylene} Lyondell MA-EVA Bynel 3101 Acid/Acrylate 0.943 3.2 DuPont Anhydride-Modified Ethylene/Vinyl Acetate Copolymer modPP Admer Maleic anhydride 0.900 3.2 Mitsui QB510A modified polypropylene modEVA SPS-33C-3 Compounded modified 0.92 1.6 MSI EVA polymer blend Technology Et-Norb 1 Topas Ethylene norbornene 0.974 1.0 Topas 9506X1 copolymer Advanced Polymers Inc. ET-Norb2 Topas 8007 Ethylene norbornene 1.02 1.7 Topas F-04 copolymer Advanced Polymers Inc. Nylon 1 Ultramid Polyamide 6 1.13 BASF B40 Nylon 2 Ultramid Polyamide 6 1.14 BASF B40LN01 Nylon 3 Ultramid Polyamide 6/66 1.13 BASF C33 01 EVA 1 Escorene Ethylene/vinyl acetate 0.933 3.5 Exxon LD 713.93 copolymer (14.4% VA) Mobil EVA 2 Escorene LD Ethylene/vinyl acetate 0.93 2.0 Exxon 318.92 copolymer (8.7% VA) Mobil EVA 3 Escorene Ethylene/vinyl acetate 0.950 5.75 Exxon LD 761.36 copolymer (26.7% VA) Mobil EVA 4 Escorene Ethylene/vinyl acetate 0.935 0.4 Exxon LD 705.MJ copolymer (12.8% VA) Mobil EVA 5 Escorene Ethylene/vinyl acetate 0.942 2.55 Exxon LD 721.IK copolymer (18.5% VA) Mobil EVA 6 Elvax 3175 Ethylene/vinyl acetate 0.950 6 DuPont copolymer (28% VA) EBA SP 1802 Ethylene/butyl acrylate 0.928 6 Eastman copolymer (22.5% BA) Chemical EVOH Soarnol Hydrolyzed ethylene 1.17 3.2 Nippon ET3803 vinyl acetate copolymer Gohsei (EVOH with 38 mol % ethylene) PVdC Saran 806 Vinylidene chloride/ 1.69 Dow methyl acrylate copolymer Sty-But Styrolux Styrene/butadiene 1.02 99 BASF 656C copolymer AOX 10555 Antioxidant in linear low 0.932 2.5 density polyethylene SLIP 1 FSU 93E Slip and antiblock in low 0.975 7.5 Schulman density polyethylene SLIP 2 1062 Ingenia Slip masterbatch amide 0.92 2 Ingenia wax (erucamide) in linear Polymers low density polyethylene WCC 11853 White color concentrate 1.513 2.90 Ampacet in linear low density polyethylene CCC 130374 Cream color concentrate Ampacet in low density polyethylene ABConc 18042 Optical brightener in 0.92 Teknor antiblock linear low density Color concentrate polyethylene procAID1 100458 Processing aid: 0.93 2.3 Ampacet fluoropolymer in polyethylene procAID2 IP 1121 Processing aid: 0.92 2 Ampacet fluoropolymer in linear low density polyethylene
Example 1 (Working)
(139) An end-seal bag was made from a coextruded, multilayer, heat-shrinkable film produced utilizing the apparatus and process set forth in
Example 1
(140) TABLE-US-00002 Layer 1 Layer 2 Layer 6 80% 70% 70% Layer 7 SSPE1 VLDPE2 Layer 3 VLDPE1 85% 20% 30% 100% Layer 4 Layer 5 30% SSPE3 LLDPE 2 EVA1 EVA1 PVDC 100% EVA3 EVA1 15% LLDPE 1 0.42 mil 0.76 mil 0.08 mil 0.18 mil 0.13 mil 0.25 mil 0.13 mils
Example 2 (Working)
(141) An end-seal bag was made from a coextruded, multilayer, heat-shrinkable film produced utilizing the apparatus and process set forth in
Example 2
(142) TABLE-US-00003 Layer 1 Layer 2 Layer 6 80% 70% 70% Layer 7 SSPE2 VLDPE1 Layer 3 VLDPE1 80% 20% 30% 100% Layer 4 Layer 5 30% SSPE3 LLDPE 2 EVA1 EVA1 PVDC 100% EVA3 EVA1 20% LLDPE 1 0.43 mil 0.78 mil 0.09 mil 0.18 mil 0.09 mil 0.26 mil 0.17 mils
Example 3 (Comparative)
(143) An end-seal bag was made from a coextruded, multilayer, heat-shrinkable film produced utilizing the apparatus and process set forth in
Example 3 (Comparative)
(144) TABLE-US-00004 Layer 1 Layer 2 Layer 3 Layer 4 100% 100% 100% 100% VLDPE3 EVA2 PVDC EVA 2 0.26 mil 1.26 mils 0.18 mil 0.6 mil
Example 4 (Comparative)
(145) An end-seal bag was made from a coextruded, multilayer, heat-shrinkable film produced utilizing the apparatus and process set forth in
Example 4 (Comparative)
(146) TABLE-US-00005 Layer 1 Layer 2 Layer 6 Layer 7 90% 80% 99% 85% SSPE1 VLDPE2 Layer 3 Layer 5 VLDPE2 SSPE3 10% 20% 100% Layer 4 100% 1% 15% SLIP1 LLDPE1 EVA1 PVDC EVA3 AOX LLDPE 1 0.44 mil 0.71 mil 0.09 mil 0.18 mil 0.09 mil 0.27 mil 0.18 mils
Example 5 (Comparative)
(147) An end-seal bag was made from a coextruded, multilayer, heat-shrinkable film produced utilizing the apparatus and process set forth in
Example 5 (Comparative)
(148) TABLE-US-00006 Layer 1 Layer 2 Layer 6 Layer 7 80% 80% 80% 80% SSPE2 VLDPE1 VLDPE1 SSPE3 20% 20% Layer 3 Layer 4 Layer 5 20% 20% LLDPE 2 VLDPE4 100% EVA1 PVDC 100% EVA3 VLDPE4 LLDPE 1 0.46 mil 1.11 mil 0.09 mil 0.18 mil 0.09 mil 0.28 mil 0.18 mils
Example 6 (Comparative)
(149) An end-seal bag was made from a coextruded, multilayer, heat-shrinkable film produced utilizing the apparatus and process set forth in
Example 6 (Comparative)
(150) TABLE-US-00007 Layer 1 Layer 2 Layer 6 90% 90% 80% SSPE1 SSPE5 Layer 3 Layer 5 SSPE5 Layer 7 10% 10% 100% Layer 4 100% 20% 100% SLIP 2 Et-PrTER EVA1 PVDC EVA3 VLDPE1 SSPE3 0.49 mil 0.89 mil 0.1 mil 0.19 mil 0.1 mil 0.26 mil 0.18 mils
Example 7 (Comparative)
(151) An end-seal bag was made from a coextruded, multilayer, heat-shrinkable film produced utilizing the apparatus and process set forth in
Example 7 (Comparative)
(152) TABLE-US-00008 Layer 1 Layer 2 Layer 3 Layer 5 Layer 6 Layer 7 100% 100% 100% Layer 4 100% 100% 85% SSPE3 ION 1 EVA1 EVA1 PVDC EVA3 SSPE4 15% LLDPE1 0.32 mil 0.87 mil 0.16 mil 0.18 mil 0.08 mil 0.21 mil 0.12 mils
Example 8
(153) An end-seal bag was made from a coextruded, multilayer, heat-shrinkable film produced utilizing the apparatus and process set forth in
Example 8
(154) TABLE-US-00009 Layer 2 Layer 3 Layer 4 84% 85% 85% Layer 1 LLDPE1 EVA2 EVA2 100% 16% 15% 15% SSPE6 CCC LLDPE1 LLDPE1 0.25 mil 1.09 mil 0.76 mil 0.25 mil
Example 9
(155) An end-seal bag was made from a coextruded, multilayer, heat-shrinkable film produced utilizing the apparatus and process set forth in
Example 9
(156) TABLE-US-00010 Layer 1 Layer 2 Layer 3 Layer 5 Layer 6 100% 100% 100% Layer 4 100% 85% EVA2 SSPE6 VLDPE2 EVA2 100% EVA2 VLDPE2 15% LLDPE1 0.31 mil 0.8 mil 0.09 mil 0.13 mil 0.4 mil 0.27 mils
Example 10
(157) An end-seal bag was made from a coextruded, multilayer, heat-shrinkable film produced utilizing the apparatus and process set forth in
Example 10
(158) TABLE-US-00011 Layer 1 Layer 3 80% 85% SSPE1 Layer 2 SSPE3 20% 100% 15% LLDPE2 EBA LLDPE1 0.08 mil 1.84 mil 0.08 mil
Example 11 (Working)
(159) An end-seal bag was made from a coextruded, multilayer, heat-shrinkable film produced utilizing the apparatus and process set forth in
Example 11 (Working)
(160) TABLE-US-00012 Layer 3 75% Layer 2 VLDPE2 75% 16.5% Layer 1 VLDPE2 LLDPE1 100% 25% 8.5% EVA 6 LLDPE1 ABConc 0.68 mil 3.08 mil 1.24 mil
Example 12 (Working)
(161) An end-seal bag marketed commercially by Curwood, Inc., under the name Protite 34 was obtained from the marketplace. Analysis of the bag from which the multilayer film was made revealed the following layers, with the order, thickness, and composition being set forth in the table below. A small cut was made into the bag skirt, i.e., as illustrated in
Example 12 (Working)
(162) TABLE-US-00013 Layer 1 Layer 3 Blend of EVA (3% vinyl Blend of EVA (3% vinyl acetate), LLDPE, and acetate), LLDPE, and metallocene-catalyzed Layer 2 metallocene-catalyzed ethylene/alpha-olefin Polyvinylidene ethylene/alpha-olefin copolymer chloride copolymer 1.53 mil 0.21 mil 0.74 mil
Example 13 (Comparative)
(163) An end-seal bag marketed commercially by Curwood, Inc., under the name Cleartite 52 was obtained from the marketplace. Analysis of the bag from which the multilayer film was made revealed the following layers, with the order, thickness, and composition being set forth in the table below. A small cut was made into the bag skirt, i.e., as illustrated in
Example 13 (Comparative)
(164) TABLE-US-00014 Layer 1 Layer 3 Blend of EVA (4% vinyl Blend of EVA (4% vinyl acetate), LLDPE, and acetate), LLDPE, and metallocene-catalyzed Layer 2 metallocene-catalyzed ethylene/alpha-olefin Polyvinylidene ethylene/alpha-olefin copolymer chloride copolymer 1.39 mil 0.23 mil 0.68 mil
Example 14 (Comparative)
(165) An end-seal bag marketed commercially by Curwood, Inc., under the name Perflex 64 was obtained from the marketplace. Analysis of the bag from which the multilayer film was made revealed the following layers, with the order, thickness, and composition being set forth in the table below. A small cut was made into the bag skirt, i.e., as illustrated in
Example 14 (Comparative)
(166) TABLE-US-00015 Layer 1 Layer 3 Blend of EVA (4% vinyl Blend of EVA (4% vinyl acetate), LLDPE, and acetate), LLDPE, and metallocene-catalyzed Layer 2 metallocene-catalyzed ethylene/alpha-olefin Polyvinylidene ethylene/alpha-olefin copolymer chloride copolymer 1.54 mil 0.19 mil 0.63 mil
Example 15 (Comparative)
(167) An end-seal bag marketed commercially by Asahi Corporation, under the name SN3 was obtained from the marketplace. Analysis of the bag from which the multilayer film was made revealed the following layers, with the order, thickness, and composition being set forth in the table below. A small cut was made into the bag skirt, i.e., as illustrated in
Example 15 (Comparative)
(168) TABLE-US-00016 Layer 2 Layer 4 Ethylene/vinyl Ethylene/vinyl acetate acetate copolymer, copolymer, Layer 5 Layer 1 containing (15 wt % Layer 3 containing (15 wt % Low Density Polyethylene vinyl Polyvinylidene vinyl Polyethylene blend acetate mer) chloride acetate mer) (possibly a blend) 0.39 mil 0.7 0.35 mil 0.66 0.63 mil
Example 16 (Working)
(169) An end-seal bag marketed commercially by Pechiney Plastic Packaging, Inc., under the name Clearshield was obtained from the marketplace. Analysis of the bag from which the multilayer film was made revealed the following layers, with the order, thickness, and composition being set forth in the table below. A small cut was made into the bag skirt, i.e., as illustrated in
Example 16 (Working)
(170) TABLE-US-00017 Layer 1 Layer 2 Layer 3 Layer 5 Layer 6 Layer 7 Metallocene- 100% Blend of Blend of 100% Blend of low catalyzed Ethylene/ polyamide Layer 4 polyamide Ethylene/ density ethylene/alpha- methyl 6 with EVOH 6 with methyl polyethylene olefin copolymer (possibly acrylate polyamide (27 mol % polyamide acrylate and linear low with LDPE or LLDPE) copolymer 6I, 6T ethylene) 6I, 6T copolymer density polyethylene 1.58 mil 0.22 mil 0.9 mil 0.21 mil 0.85 mil 0.16 mil 0.57 mil
Example 17 (Working)
(171) An end-seal bag was made from a coextruded, multilayer, heat-shrinkable film produced utilizing the apparatus and process set forth in
Example 17 (Working)
(172) TABLE-US-00018 Layer 1 Layer 3 Layer 6 Layer 7 90% 50% 80% 80% SSPE1 Layer 2 EVA4 VLDPE1 SSPE3 10% 100% 50% Layer 4 Layer 5 20% 20% SLIP2 Ion&Eva&PB LLDPE1 100% PVdC 100% EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 18 (Working)
(173) TABLE-US-00019 Layer 1 Layer 3 Layer 6 Layer 7 90% 50% 80% 80% SSPE1 EVA4 Layer 4 VLDPE1 SSPE3 10% Layer 2 50% 100% Layer 5 20% 20% SLIP2 100% EVA&PP LLDPE1 PVdC 100% EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 19 (Working)
(174) TABLE-US-00020 Layer 1 Layer 2 Layer 3 Layer 6 Layer 7 90% 75% 50% 80% 80% SSPE1 EVA2 EVA4 VLDPE1 SSPE3 10% 25% 50% Layer 4 Layer 5 20% 20% SLIP2 modEVA LLDPE1 100% PVdC 100% EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 20 (Working)
(175) TABLE-US-00021 Layer 1 Layer 3 Layer 6 Layer 7 90% 50% 80% 80% SSPE1 EVA4 VLDPE1 SSPE3 10% Layer 2 50% Layer 4 Layer 5 20% 20% SLIP2 100% Et-Norb2 LLDPE1 100% PVdC 100% EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 21 (Working)
(176) TABLE-US-00022 Layer 1 Layer 3 Layer 6 Layer 7 90% 50% 80% 80% SSPE1 EVA4 VLDPE1 SSPE3 10% Layer 2 50% Layer 4 Layer 5 20% 20% SLIP2 100% Et-Norb1 LLDPE1 100% PVdC 100% EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 22 (Comparative)
(177) TABLE-US-00023 Layer 1 Layer 3 Layer 6 Layer 7 90% 50% 80% 80% SSPE1 Layer 2 EVA4 Layer 4 Layer 5 VLDPE1 SSPE3 10% 100% 50% 100% 100% 20% 20% SLIP2 Sty-But LLDPE1 PVdC EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 23 (Working)
(178) TABLE-US-00024 Layer 1 Layer 3 Layer 6 Layer 7 90% 50% 80% 80% SSPE1 Layer 2 EVA4 Layer 4 Layer 5 VLDPE1 SSPE3 10% 100% 50% 100% 100% 20% 20% SLIP2 PP1 LLDPE1 PVdC EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 24 (Working)
(179) TABLE-US-00025 Layer 1 Layer 2 Layer 3 Layer 6 Layer 7 90% 70% 50% 80% 80% SSPE1 Sty-But EVA4 Layer 4 Layer 5 VLDPE1 SSPE3 10% 30% 50% 100% 100% 20% 20% SLIP2 EVA5 LLDPE1 PVdC EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 25 (Working)
(180) TABLE-US-00026 Layer 1 Layer 2 Layer 3 Layer 6 Layer 7 90% 70% 50% 80% 80% SSPE1 Sty-But EVA4 Layer 4 Layer 5 VLDPE1 SSPE3 10% 30% 50% 100% 100% 20% 20% SLIP2 EVA2 LLDPE1 PVdC EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 26 (Working)
(181) TABLE-US-00027 Layer 1 Layer 2 Layer 6 Layer 7 90% 70% Layer 3 80% 80% SSPE1 VLDPE2 50% EVA4 VLDPE1 SSPE3 10% 30% 50% Layer 4 Layer 5 20% 20% SLIP2 ET-Norb2 LLDPE1 100% PVdC 100% EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 27 (Working)
(182) TABLE-US-00028 Layer 1 Layer 2 Layer 3 Layer 6 Layer 7 90% 70% 50% 80% 80% SSPE1 ssPP EVA4 Layer 4 Layer 5 VLDPE1 SSPE3 10% 30% 50% 100% 100% 20% 20% SLIP2 SSPE3 LLDPE1 PVdC EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mil.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 28 (Working)
(183) TABLE-US-00029 Layer 1 Layer 2 Layer 3 Layer 6 Layer 7 90% 70% 50% 80% 80% SSPE1 ssPP EVA4 Layer 4 Layer 5 VLDPE1 SSPE3 10% 30% 50% 100% 100% 20% 20% SLIP2 EVA2 LLDPE1 PVdC EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 29 (Working)
(184) TABLE-US-00030 Layer 1 Layer 2 Layer 3 Layer 6 Layer 7 90% 80% 50% 80% 80% SSPE1 SSPE3 EVA4 Layer 4 Layer 5 VLDPE1 SSPE3 10% 20% 50% 100% 100% 20% 20% SLIP2 WCC LLDPE1 PVdC EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 30 (Working)
(185) TABLE-US-00031 Layer 1 Layer 3 Layer 6 Layer 7 90% 50% 80% 80% SSPE1 Layer 2 EVA4 Layer 4 Layer 5 VLDPE1 SSPE3 10% 100% 50% 100% 100% 20% 20% SLIP2 ION 2 LLDPE1 PVdC EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 31 (Working)
(186) TABLE-US-00032 Layer 1 Layer 3 Layer 6 Layer 7 90% 50% 80% 80% SSPE1 Layer 2 EVA4 Layer 4 Layer 5 VLDPE1 SSPE3 10% 100% 50% 100% 100% 20% 20% SLIP2 EVA6 LLDPE1 PVdC EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 32 (Working)
(187) TABLE-US-00033 Layer 1 Layer 3 Layer 6 Layer 7 90% 50% 80% 80% SSPE1 Layer 2 EVA4 Layer 4 Layer 5 VLDPE1 SSPE3 10% 100% 50% 100% 100% 20% 20% SLIP2 PB LLDPE1 PVdC EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 33 (Working)
(188) TABLE-US-00034 Layer 1 Layer 2 Layer 3 Layer 6 Layer 7 90% 85% 50% 80% 80% SSPE1 SSPE1 EVA4 VLDPE1 SSPE3 10% 15% 50% Layer 4 Layer 5 20% 20% SLIP2 RECLAIM LLDPE1 100% PVdC 100% EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 34 (Working)
(189) TABLE-US-00035 Layer 1 Layer 2 Layer 3 Layer 6 Layer 7 90% 70% 50% 80% 80% SSPE1 SSPE1 EVA4 VLDPE1 SSPE3 10% 30% 50% Layer 4 Layer 5 20% 20% SLIP2 RECLAIM LLDPE1 100% PVdC 100% EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
Example 35
(190) TABLE-US-00036 Layer 1 Layer 2 Layer 3 Layer 6 Layer 7 90% 55% 50% 80% 80% SSPE1 SSPE1 EVA4 VLDPE1 SSPE3 10% 45% 50% Layer 4 Layer 5 20% 20% SLIP2 RECLAIM LLDPE1 100% PVdC 100% EVA3 VLDPE4 LLDPE1 3.0 mil.sup.t 3.7 mil.sup.t 11.4 mil.sup.t 2.2 mil.sup.t 1 mil.sup.t 1.5 mils.sup.t 1.5.sup.t .sup.tthickness in table represents thickness of extrudate before solid state orientation at trapped bubble stage of process
(191) A seamless film tubing of each of the films of Examples 1-35 is cut and sealed to form an end-seal bag. A small cut was made in the bag skirt, about 1 to 2 inches from the folded bag side edge. The bag skirt had a width of about 1.5 inches. A product was placed in the bag, and the bag was sealed closed and shrunk around the product. The resulting end-seal bags exhibit the following characteristics.
(192) TABLE-US-00037 Peak Load Impact Free Straight, LD Tear LD Tear Strength Total Shrink Full Propagation Propagation LD Tear per mil, via Bag of Film at 185 F. Length Max Load Energy to Resistance ASTM D Example Gauge (% MD/ Manual (gmf, i.e., Break Max Load 3763-95A No. (mils) % TD) MD Tear grams force) (gmf-in) (gmf) (N/mil) 1 2.0 32/45 Yes 31 545 98 2 2.0 35/51 Yes 23 31 598 114* 3 2.3 No 22 36 673 54.9* 4 1.96 No 31 39 566 102.6* 5 2.4 No 54 58 791 100* 114.3* 137.2* 6 2.2 No 61 68 625 138.7* 104.5* 7 1.9 No 28 34 659 102* 8 2.35 17/28 24.8 113* 9 2.0 26/42 110* 10 2.0 11 5.0 Yes 50 86 1470 105* 12 2.18 32/40 Yes 20 38 840 116.3 13 2.03 35/39 No 22 35 732 73.9 14 2.18 22/30* No 23 44 732 15 2.47 50/50 No 279 330 685 71.9 16 4.6 Yes 284 440 3110 155.0 17 2.42 24/36 Yes 35 747 18 2.48 19/36 Yes 205 797 19 2.48 20/35 Yes 23 817 20 Yes 21 2.56 23/33 Yes 21 30 676 22 2.53 24/36 No 40 726 23 2.53 20/33 Yes 21 29 724 24 2.5 23/34 Yes 32 47 848 25 2.5 22/34 Yes 22 35 707 26 2.51 24/32 Yes 20 27 723 27 2.39 18/32 Yes 13 23 843 28 2.36 15/34 Yes 21 820 29 2.39 17/34 Yes 17 30 643 30 2.29 Yes 71.0 81 551 31 2.31 Yes 15.3 557 32 2.18 Yes 113.0 140 693 33 2.55 Yes 55.0 50 427 34 2.41 Yes 57.3 55 477 35 2.45 Yes 40.2 46 638 *impact strength tested on different sample of film with same designation