NZ202957A - Aluminium foil/ethylene copolymer laminate web and containers made therefrom - Google Patents
Aluminium foil/ethylene copolymer laminate web and containers made therefromInfo
- Publication number
- NZ202957A NZ202957A NZ202957A NZ20295783A NZ202957A NZ 202957 A NZ202957 A NZ 202957A NZ 202957 A NZ202957 A NZ 202957A NZ 20295783 A NZ20295783 A NZ 20295783A NZ 202957 A NZ202957 A NZ 202957A
- Authority
- NZ
- New Zealand
- Prior art keywords
- copolymer
- ethylene
- web
- container
- poly
- Prior art date
Links
- 229920001038 ethylene copolymer Polymers 0.000 title description 3
- 239000005030 aluminium foil Substances 0.000 title 1
- 239000011888 foil Substances 0.000 claims description 39
- 229920001577 copolymer Polymers 0.000 claims description 24
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 18
- 239000005977 Ethylene Substances 0.000 claims description 18
- 229910052782 aluminium Inorganic materials 0.000 claims description 16
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 14
- 230000003412 degenerative effect Effects 0.000 claims description 12
- -1 poly(ethylene/acrylic acid) Polymers 0.000 claims description 11
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 10
- 229920002125 Sokalan® Polymers 0.000 claims description 10
- 239000004584 polyacrylic acid Substances 0.000 claims description 10
- 229920000642 polymer Polymers 0.000 claims description 10
- 229910052804 chromium Inorganic materials 0.000 claims description 9
- 239000011651 chromium Substances 0.000 claims description 9
- 238000007765 extrusion coating Methods 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 239000000758 substrate Substances 0.000 claims description 7
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 6
- 229920000554 ionomer Polymers 0.000 claims description 5
- 239000000155 melt Substances 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 4
- 125000004185 ester group Chemical group 0.000 claims description 4
- 229920005989 resin Polymers 0.000 claims description 4
- 239000011347 resin Substances 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 3
- 230000001476 alcoholic effect Effects 0.000 claims description 3
- 239000004075 cariostatic agent Substances 0.000 claims description 3
- 239000000551 dentifrice Substances 0.000 claims description 3
- 238000001125 extrusion Methods 0.000 claims description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 2
- 229920001903 high density polyethylene Polymers 0.000 claims description 2
- 239000004700 high-density polyethylene Substances 0.000 claims description 2
- 238000000151 deposition Methods 0.000 claims 2
- 238000010438 heat treatment Methods 0.000 claims 2
- 238000001816 cooling Methods 0.000 claims 1
- 239000000047 product Substances 0.000 description 21
- 239000010410 layer Substances 0.000 description 19
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 16
- 239000002987 primer (paints) Substances 0.000 description 15
- 239000004698 Polyethylene Substances 0.000 description 8
- 229920000573 polyethylene Polymers 0.000 description 8
- 238000003860 storage Methods 0.000 description 8
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 239000010445 mica Substances 0.000 description 6
- 229910052618 mica group Inorganic materials 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 230000032798 delamination Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000004806 packaging method and process Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000000606 toothpaste Substances 0.000 description 4
- 229940034610 toothpaste Drugs 0.000 description 4
- 229920012753 Ethylene Ionomers Polymers 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000004568 cement Substances 0.000 description 3
- 238000005336 cracking Methods 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 229920001684 low density polyethylene Polymers 0.000 description 3
- 239000004702 low-density polyethylene Substances 0.000 description 3
- 239000000123 paper Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 230000006353 environmental stress Effects 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 239000013615 primer Substances 0.000 description 2
- 230000037452 priming Effects 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 238000004826 seaming Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229920003182 Surlyn® Polymers 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000007850 degeneration Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229940063559 methacrylic acid Drugs 0.000 description 1
- 125000005395 methacrylic acid group Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000012260 resinous material Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- ANOBYBYXJXCGBS-UHFFFAOYSA-L stannous fluoride Chemical compound F[Sn]F ANOBYBYXJXCGBS-UHFFFAOYSA-L 0.000 description 1
- 229960002799 stannous fluoride Drugs 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B3/00—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form
Landscapes
- Laminated Bodies (AREA)
- Tubes (AREA)
- Wrappers (AREA)
- Containers Having Bodies Formed In One Piece (AREA)
Description
New Zealand Paient Spedficaiion for Paient Number £02957
202957
Priority Date(s): J%. '. J:.$R
Complete Specification Filed: &*;J.
Class:
3&$4&$/0Q...
Publication Date: ... HAP. J
P.O. Journal, No: .iSfrJ
NO iRAllNgS
m 6 JAN 1983 Receives ~~~
Patents form No. 5
NEW ZEALAND PATENTS ACT 1953 COMPLETE SPECIFICATION
"LAMINATE WEB PRODUCED WITH POLYACRYLIC ACID COMPLEX PRIMER"
<f,WE AMERICAN CAN COMPANY, a corporation organized and existing under the laws of the State of New Jersey, of American Lane, Greenwich, Connecticut, 06830, United States of America,
hereby declare the invention, for which /we pray that a patent may be granted to p^/us, and the method by which it is to be performed, to be particularly described in and by the following statement:-
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BACKGROUND OF THE INVENTION
Tubes and other containers made of laminated webs, that ar^ in turn fabricated from a metal foil and layers of synthetic resinous materials, are widely used for the packaging of a variety of products, such as toothpaste and the like; American Can Company, of Greenwich, Connecticut, markets such tubular containers under its GLAMINATE trademark. By properly designing and constructing the laminate, the oxygen and moisture barrier properties necessary for the containment of many commodities are afforded, as are the heat sealability arid dead fold characteristics that are desirable in a tube-like package. Typically, the product side of the laminate web will comprise an oiefiriicpolymer, such as low density polyethylene, ethylene-acrylic acid copolymer (EAA) or Surlyn ionomer, bonded to the inner surface of the metal layer, which is normally aluminum foil.
although' containers so constructed are entirely - — satisfactory under most circumstances, the ingredients of certain products have a tendency to degrade or otherwise attack the materials of construction, causing failure of the container. Certain dentifrice products are notoriously difficult to package in such a laminate web structure, particularly those that contain stannous or sodium fluoride as an anticaries agent. Due to the acid environment and/or the essential flavoring oils and detergents that are present, there is a strong tendency for ingredients of the toothpast to permeate the inner plastic layer, and to migrate to the interface, thereby promoting delamination in the web structure and causing deterioration of the contained
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2 02 95 7
product. Of course, the longer the period of storage the more pronounced will be the tendency for degeneration to occur in the laminate web, and particularly so if the packaged is stored at a relatively elevated temperature.
Various measures have teen: taken in the past not only to enhance the initial level of adhesion achieved between the plastic film and the foil, but also to improve resistance to delamination over extended storage periods, i.e., to extend shelf life. These efforts include flame treatment of the foil, the utilization of interlayers of various adhesive materials, and chemical priming of the metal to increase the strength of the bond at the interface. A notable example of the latter approach entails the utilization of a polyacrylic acid chromium complex product as a foil primer to promote adhesion to polyethylene; laminate structures so produced have been used for the packaging of alcohol-saturated swabs. While the utilization of such a primer^Ts"seen™to significantly enhance,bond strength," still it is not entirely satisfactory on long-term storage, and the use of polyethylene as the product-side layer may be undesirable in some instances, due to the tendency of that material to show environmental stress cracking in the presence of certain " products, such as toothpaste.
Accordingly, it is a primary object of the present invention to provide a novel laminate web comprised of aluminum foil and a layer of a copolymer of ethylene with an acrylic acid or acrylic acid ester monomer, which web is adapted for use to contain degenerative products for extended periods of time.
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It is also an object of the invention to provide a novel container and package fabricated from such a laminate web.
Additional objects of the invention are to provide novel methods for the production of such webs, containers and packages.
SUMMARY OF THE INVENTION It has now been found that certain of the foregoing and related objects of the invention are readily attained by the provision of a laminate web comprising aluminum foil, a film of a copolymer of ethylene having in its molecule pendant carboxylic acid or ester groups, and a layer of a polyacrylic acid chromium complex primer therebetween. In preferred embodiments of the web,„the..copolymer of the film will be selected from the group consisting of poly(ethylene/acrylic acid), poly(ethylene/meth-acrylic acid), poly(ethylene/methylacrylate), poly(ethylene/ methyl methacrylate), poly(ethylene/vinyl acetate), and ionomer resins. _.The__primer coating will be of at least monomolecular thickness,"and" the web will generally comprise at least one additional layer; normally it will include at least one synthetic resinous polymer layer disposed upon the side of the foil opposite to that upon which the primer is applied.
Other objects of the invention are attained by the practice of a method for the production of a laminate web, wherein at least a monomolecular layer of a polyacrylic acid chromium complex primer, formulated as an aqueous alcoholic solution, is deposited upon at least one side of an aluminum foil substrate, rhe coated substrate is thereafter heated to substantially dry the primer, following which a film of a copolymer of ethylene (as described above) is extrusion coated upon the primed surface; the y
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laminate is cooled to provide the finished web. Preferably, in the extrusion coating step, the copolymer melt will have a temperature of about 550° to 600° Fahrenheit, and most desirably its temperature will be at about 575° to 590° Fahrenheit.
Additional objects of the invention are realized by the provision of a container for a degenerative product, which container is fabricated from a laminate web constructed as described, and having the copolymer film disposed on the product side thereof. Other objects are obtained in such a container filled with a degenerative product, maximum benefit in this regard often being realized when the contained product is a dentrifice substance containing a fluoride anticaries agent and/or one or'more essential oils. Usually, such a container will be in the form of a tube, with the laminate web constituting the sidewall and with a headpiece bonded within one end of the tubular structure; the headpiece will generally be made of a polyolefin.resin, such as high density polyethylene. Still • -: further objects of the invention are attained in a method for the production of a container, and in a packaging method utilizing the same, in accordance with which the above-described laminate web is formed into a container structure with the copolymer film disposed on the inside surface, and the container being filled with a degenerative product.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
As noted initially, foil/ethylene copolymer laminate webs have previously been used for container fabrication. The present invention provides means by which the strength of the bond between the foil and the copolymer layer on the product side is
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greatly enhanced, and is rendered substantially less susceptible to degenerative ingredients that may migrate to the interface.
The chrome complexes that are utilized to prime the aluminum foil surface are commercially available from the Mica Corporation, of Stamford, Connecticut, under the trade designation MICA A-291, which is a seven percent aqueous solution of a polyacrylic acid chromium complex; it is acidic in nature and has a viscosity of about ten centipoise. . The MICA A-291 product literature indicates use for bonding polyethylene to aluminum foil, for packaging and industrial applications requiring high bonds and resistance to a variety of hard-to-hold materials, including fluorides and essential pi-Is. It is not -believed, however, that there has heretofore been any recognition that the use of such a primer will achieve the results attained by the instant process; i.e., the development of extremely durable ibonds between aluminum foil and extrusion coatings of carboxcylic acid or ester-containing copolymers of ethylene, which bonds endure despite intimate contact with products considered to be of a highly degenerative nature.
Although the above-identified chromium complex is believed to be the most effective primer for use herein, other closely-related substances may be substituted if so desired. Thus, the length of the polyacrylic acid chain may vary, as may the proportion of"the acrylic acid moiety in the copolymer and the ratio of the metal to the organic portion of the complex. Indeed, it is possible that other transition metals, such as cobalt, copper, nickel, and the like, might be substituted for the chrome ion.
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As indicated above, the primer will generally be applied a dilute water/alcohol solution, to maximize leveling and wettii»_ of the substrate, and thereby afford optimal levels of adhesion of the polymer layer thereto. To prepare the working liquid, th-~ commercial MICA A-291 product may suitably be mixed with .additional water and isopropyl alcohol in a volumetric ratio of 30: 60: 10, respectively.
The resulting solution will be used in an amount suffician" to—provide,- when dried, about 0.03 to~0i08, and preferably about 0.035, pound of complex solids per ream (i.e., 3,000 square feet of surface area). In any event, the primer must be of at least monomolecular thickness, and generally it will be at least some-! what heavier. After drying of the primer, typically by passage of the foil structure through an oven held at a suitable temperature, (i.e., about 250° to 400° Fahrenheit), the web may be presented .directly to a-copolymer extrusion station; at that point, its temperature will generally be about 100° to 150° Fahrenheit.
The techniques utilized for extrusion coating of the ethylene copolymer upon the aluminum foil are well known to those skilled in the art, and need not be discussed in detail. It should, however, be appreciated that the temperature of the melt is critical to the attainment of optimal bonding, bearing in mind that the copolymer must not only be strongly adhered to the foil, but that its capacity for self-bonding (i.e., for heat sealing) and for bonding to other portions of the ultimate container must also be preserved. Specifically, and as has been pointed out above, the laminate webs of the invention will find there widest utility in the production of tubular containers, for which
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applications the web must be capable of side seaming and secure attachment to the molded headpiece. High melt temperatures favor bonding to the foil; on the other hand, they also promote oxidation, which inhibits the formation of good bonds with other polymeric surfaces (e.g., the headpiece). Consequently (and depending to an extent upon the air gap distance beyond the. extruder die lips) , EAA will generally be extruded, in the practice of the present method, at a temperature of 550° to 600° Fahrenheit^ and an optimum balance of ^bonding properties will usually be realized with a melt temperature of about 575° to 590° Fahrenheit.
While EAA or ionomer will usually constitute the:
product-side layer in the laminate web, other copolymers of ethylene having pendant carboxylic acid or ester groups can also be used, such as copolymers with acrylic or methacrylic acids, methylacrylate, methylmethacrylate, and vinyl acetate.; The techique normally used to produce the foil/copoiymer composite will be extrusion coating in view of the recognized economic and practical benefits of doing so; however, other techniques may be found to be feasible under certain circumstances, and may be employed if so desired. Generally, the thickness of the product-side polymer will.range from about 1.0 to 4.0, and more commonly 1.5 to 3.0, mils, to provide an optimal functional and economic balance.
Insofar as the foil component is concerned, as a practical matter thin-gauge (i.e., about 0.285 to 3.0 mils) aluminum will normally be utilized, although for certain applications foils of other metals might be substituted. The laminate web will
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generally contain additional polymer layers for various purposes, and a paper layer will usually be included to enable facile printing or decoration of the article. A typical laminate profile will comprise (from the outside in): polyethylene, paper, polyethylene, EAA, foil, primer, and EAA, which structure is (save for the foil, primer, EAA subcombination) conventional and not an essential aspect of the present invention. Similarly, the manner in which the laminate web is converted into the container (e.g., head bonding, side seaming, and end sealing to form and close a tube) may be entirely conventional and known to those skilled in the art; accordingly, detailed description is unnecessary. It might be mentioned, however, that in forming the
- overlap - , - _•■•••
side seam it is common practice to the edges of the web.
Since this will expose both sides of the laminate to the product, advantage can be seen in priming both surfaces of the foil, in accordance herewith.
Exemplary of the efficacy of the present invention are the1 following specific examples:
EXAMPLE ONE
Webs are produced utilizing a laminate subassembly ~ comprised of layers of polymers and paper bonded to 0.7 mil of aluminum foil, the overall gauge of the subassembly being about 10.2 mils. The exposed side of the foil is primed by applying, from a rotogravure cylinder, somewhat in excess of a monomolecular layer of a polyacrylic acid chromium complex, using a 30: 60: 10 solution of MICA A-291: water: isopropyl alcohol, which is subsequently forced air dried in an oven, at about 250° Fahrenheit.
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A first laminate is produced by extrusion coating the primed foil surface with 43.5 pounds per ream of low density polyethylene, the extrudate being at a temperature of about 600° Fahrenheit; the laminate is designated "A". A second laminate, designated "B", is prepared by extrusion coating the subassembly with the same thickness of an EAA copolymer containing 3.5 percent of the acrylic acid monomer, the temperature of the melt also being about 600° Fahrenheit; a third web (laminate "C"), is prepared in the same manner utilizing, in place of the 3.5 percent resin, an EAA copolymer containing 8.0 percent of the acrylic acid moiety.
The foregoing laminates are converted to small pillows measuring 1 x 5-5/8 inches, which are filed with a commercial dentifrice product (i.e.. Proctor & Gamble CREST toothpaste), and. are thereafter sealed. Several pillows produced from each of the three laminates are held at a controlled temperature for -periods-*-
of from two weeks to six months, after which the condition of the web is determined. Specifically, five pillows of each sample are held at temperatures of 75° and 105° Fahrenheit, and three pillows of each sample are held at a temperature of 120°
t
Fahrenheit; they are evaluated at intervals of two, four, eight, twelve, and twenty-six weeks. The results are set forth in Table One, which follows:
fO
LAMINATE
TABLB ONB
Peiod (Weeks)i Tea; erature (° F) i
2 Weeks
4 Weeks
8 Weeks
12 Weeks
26 Weeks
75 105 120 75 105 120 75 105 120 75 105 120 75 105 120
G-E F
G-E F P-F G F
P-F
B
G-E
G-E G-E G-E G-E F
G-E G-E
G-E F-G
G-E
G-E G-E G-E G-E G
G-E G-E
G-E G-E
M
O
NJ
sO
Ul
N|
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As used in the Table, the designations "E", "G", "F", and "P", mean that the condition of the web is judged to be excellent, good, fair, or poor, respectively; a dash mark indicates that no test is performed under the indicated conditions. To be considered excellent, the level of adhesion must be such that the pdlymer layer becomes stretched in endeavoring to separate it form the foil. Good adhesion 'indicates that separation is achieved and sustained only with difficulty. If the laminate offers a significant amount of resistance to separation it __is. deemed to be fair, and if it is easily delaminated the level of adhesion is regarded to be poor.
From Table One, it is seen that surprisingly high levels of bond strength are achieved utilizing the EAA film on the primed foil (laminates "B* and "C") , as compared to that which is exhibited when the laminated polymer is polyethylene (laminate "A"). More particularly, after storage for four weeks at 120°_ Fahrenheit,;- and 8 or 12 weeks at 105° Fahrenheit, the - " EAA-containing laminates both exhibit good-to-excellent adhesion, whereas the polyethylene web has only fair bond strength. While these are the most dramatic differences reflected in Table One, it can be seen, that. in all instances the EAA laminates are " invariably superior to those made with the low density polyethylene.
In addition to the foregoing delamination tests, environmental stress cracking of the three laminate webs is evaluated by hand squeezing selected pillows. After six months storage time at 105° Fahrenheit, the pillows produced from the polyethylene web are found to be highly prone to cracking when
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manually squeezed. In contrast, the EAA—based laminates, conditioned in the same way, satisfactorily survive such manipulation.
EXAMPLE TWO
A commercial household cement product (i.e., duPont DUCO cement) is sealed within pouches 'produced from laminates containing either 3.5 percent EAA or ionomer on aluminum foil, the polymer and foil gauges being 2.0 and 0.332 mil; respectively, in all cases. Two versions of each laminate are produced; i.e., both with and without pretreatment of the foil with the MICA A-291 primer. The pouches are sealed and stored at a temperature of 105° Fahrenheit, different ones being opened after one and two months' storage time to assess the levels of adhesion that are maintained between the polymer layer and the foil. . ■ .. ...
. - After.:storage: for - one- raonthV"-:;tli"e^ ^ebs- made wi;feh--the-; prim"ed'
aluminum show good adhesion regardless of whether the polymer layer, is comprised, of EAA or ionomer. The unprimed aluminum, on the other hand, produces webs in which delamination (in the case of EAA) or poor adhesion (in the case of the ionomer) occurs J The results are the same following the two-months storage period.
Although the foregoing specific examples demonstrate the outstanding ability of the instant laminate webs to withstand the degenerative effects of a fluoride toothpaste and a household cement containing highly active organic solvents, it should be appreciated that the instant webs can be used advantageously for the containment of a wide range of other products deemed to be
/ 1
202957
Claims (13)
1. A laminate web suitable for use in producing containers for degenerative products, comprising aluminum foil, a film of a copolymer of ethylene having in its molecule pendant carboxylic acid or ester groups, and at least a monomolecular layer of a polyacrylic acid chromium complex primer therebetween.
2. The web of claim 1, wherein said copolymer is selected from the group consisting of poly(ethylene/acrylic 10 acid), poly(ethylene/methacrylic acid), poly(ethylene/methyl acrylate), poly(ethylene/methyl methacrylate), poly(ethylene/ vinyl acetate), and ionomer.
3. The web of claim 1 or claim 2, wherein said web additionally includes a film of a synthetic resinous polymer upon the side of said foil opposite to that upon which said primer layer is applied.
4. In a method for the production of a laminate web suitable for use in producing containers for degenerative products, the steps including: depositing upon at least one 20 surface of an aluminum foil substrate at least a monomolecular layer of a polyacrylic acid chromium complex primer, as an aqueous alcoholic solution; heating said coated substrate to substantially dry said primer; extrusion coating a film of a copolymer of ethylene upon at least one of said primed surfaces of said foil, said copolymer having pendant carboxylic acid or ester groups in its molecule; and cooling the laminate to provide said web.
5. The method of claim 4, wherein said copolymer is selected from the group consisting of poly(ethylene/acrylic 30 acid) and ionomer resin. 202957
6. The method of claim 5, wherein said copolymer is poly(ethylene/acrylic acid), and wherein said copolymer exits from the extrusion dye at a melt temperature of 550° to 600° Fahrenheit.
7. The method of claim 6, wherein said melt temperature is 575° to 590° Fahrenheit.
8. A container for a degenerative product fabricated from the laminate web of any one of claims 1 to 3, wherein said copolymer film is on the product side of said container.
9. A package comprised of the container of claim 8, said package including a degenerative product contained therewithin.
10. The package of claim 9, wherein said product is a dentifrice substance containing a fluoride anticaries agent.
11. The container of any one of claims 8 to 10, wherein said laminate web is formed into a tubular configuration, and wherein said container additionally includes a headpiece secured to one end of said tubular structure.
12. The container of claim 11, wherein said headpiece is fabricated from high density polyethylene.
13. In a method for the production of a container for a degenerative product, the steps comprising: depositing upon at least one surface of an aluminum foil substrate at least a monomolecular layer of a polyacrylic acid chromium complex primer, as an aqueous alcoholic solution; heating said coated substrate to substantially dry said primer; extrusion coating at a melt temperature of 550° to 600° Fahrenheit, a film of a copolymer of ethylene upon at least one of said primed surfaces of said foil, said copolymer
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US34046882A | 1982-01-18 | 1982-01-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
NZ202957A true NZ202957A (en) | 1986-03-14 |
Family
ID=23333479
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NZ202957A NZ202957A (en) | 1982-01-18 | 1983-01-06 | Aluminium foil/ethylene copolymer laminate web and containers made therefrom |
Country Status (17)
Country | Link |
---|---|
JP (2) | JPS58124642A (en) |
KR (1) | KR900004782B1 (en) |
AR (1) | AR240951A1 (en) |
BR (1) | BR8300184A (en) |
CA (1) | CA1201050A (en) |
DK (1) | DK162753C (en) |
ES (1) | ES530166A0 (en) |
GR (1) | GR77880B (en) |
IE (1) | IE54134B1 (en) |
IL (1) | IL67555A (en) |
IN (2) | IN159631B (en) |
MX (2) | MX163612B (en) |
NO (1) | NO161965C (en) |
NZ (1) | NZ202957A (en) |
PH (1) | PH20707A (en) |
PT (1) | PT76096B (en) |
ZA (1) | ZA829458B (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0721338U (en) * | 1994-09-12 | 1995-04-18 | 大日本印刷株式会社 | Low-odor packaging material manufacturing method |
JP4499071B2 (en) * | 1996-10-02 | 2010-07-07 | 大成化工株式会社 | Metal extruded tube, its production method and its use |
KR20010011802A (en) * | 1999-07-30 | 2001-02-15 | 조문수 | Surface sheet, sandwich structure, article using |
CN114955047A (en) * | 2022-07-01 | 2022-08-30 | 深圳市红标点科技有限公司 | Composite kraft paper coating method for bundled books |
-
1982
- 1982-09-28 CA CA000412377A patent/CA1201050A/en not_active Expired
- 1982-09-29 JP JP57170827A patent/JPS58124642A/en active Granted
- 1982-12-23 ZA ZA829458A patent/ZA829458B/en unknown
- 1982-12-24 IL IL67555A patent/IL67555A/en not_active IP Right Cessation
- 1982-12-28 IN IN1496/CAL/82A patent/IN159631B/en unknown
-
1983
- 1983-01-06 NZ NZ202957A patent/NZ202957A/en unknown
- 1983-01-11 GR GR70235A patent/GR77880B/el unknown
- 1983-01-12 AR AR291843A patent/AR240951A1/en active
- 1983-01-14 NO NO830112A patent/NO161965C/en unknown
- 1983-01-17 MX MX195924A patent/MX163612B/en unknown
- 1983-01-17 BR BR8300184A patent/BR8300184A/en not_active IP Right Cessation
- 1983-01-17 PT PT76096A patent/PT76096B/en unknown
- 1983-01-17 PH PH28625A patent/PH20707A/en unknown
- 1983-01-17 IE IE79/83A patent/IE54134B1/en not_active IP Right Cessation
- 1983-01-18 DK DK018983A patent/DK162753C/en not_active IP Right Cessation
- 1983-01-18 KR KR1019930000167A patent/KR900004782B1/en not_active IP Right Cessation
-
1984
- 1984-02-29 ES ES530166A patent/ES530166A0/en active Granted
-
1986
- 1986-03-27 IN IN249/CAL/86A patent/IN162390B/en unknown
-
1990
- 1990-04-17 JP JP2099456A patent/JPH03646A/en active Granted
-
1991
- 1991-07-10 MX MX9100155A patent/MX9100155A/en unknown
Also Published As
Publication number | Publication date |
---|---|
IN159631B (en) | 1987-05-30 |
IL67555A (en) | 1988-03-31 |
IN162390B (en) | 1988-05-21 |
AR240951A1 (en) | 1991-03-27 |
MX163612B (en) | 1992-06-05 |
AR240951A2 (en) | 1991-03-27 |
JPH0555380B2 (en) | 1993-08-16 |
PT76096A (en) | 1983-02-01 |
DK162753B (en) | 1991-12-09 |
ZA829458B (en) | 1984-02-29 |
NO161965C (en) | 1989-10-18 |
DK162753C (en) | 1992-04-27 |
KR840003069A (en) | 1984-08-13 |
JPH03646A (en) | 1991-01-07 |
BR8300184A (en) | 1983-10-11 |
NO830112L (en) | 1983-07-19 |
IE54134B1 (en) | 1989-06-21 |
NO161965B (en) | 1989-07-10 |
DK18983A (en) | 1983-07-19 |
PH20707A (en) | 1987-03-30 |
JPH0259056B2 (en) | 1990-12-11 |
PT76096B (en) | 1986-03-18 |
GR77880B (en) | 1984-09-25 |
ES8502904A1 (en) | 1985-02-01 |
DK18983D0 (en) | 1983-01-18 |
CA1201050A (en) | 1986-02-25 |
IE830079L (en) | 1983-07-18 |
MX9100155A (en) | 1993-01-01 |
KR900004782B1 (en) | 1990-07-05 |
ES530166A0 (en) | 1985-02-01 |
JPS58124642A (en) | 1983-07-25 |
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