IE54134B1 - Laminates incorporating a polyacrylic acid caomplex primer, packaging or containers made therefrom and manufacture of said laminates - Google Patents
Laminates incorporating a polyacrylic acid caomplex primer, packaging or containers made therefrom and manufacture of said laminatesInfo
- Publication number
- IE54134B1 IE54134B1 IE79/83A IE7983A IE54134B1 IE 54134 B1 IE54134 B1 IE 54134B1 IE 79/83 A IE79/83 A IE 79/83A IE 7983 A IE7983 A IE 7983A IE 54134 B1 IE54134 B1 IE 54134B1
- Authority
- IE
- Ireland
- Prior art keywords
- web
- ethylene
- foil
- primer
- copolymer
- Prior art date
Links
- 229920002125 Sokalan® Polymers 0.000 title claims abstract description 15
- 239000004584 polyacrylic acid Substances 0.000 title claims abstract description 15
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 238000004806 packaging method and process Methods 0.000 title claims description 6
- 239000011888 foil Substances 0.000 claims abstract description 39
- 229920001577 copolymer Polymers 0.000 claims abstract description 29
- 238000000034 method Methods 0.000 claims abstract description 18
- 230000003412 degenerative effect Effects 0.000 claims abstract description 16
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 10
- 239000011651 chromium Substances 0.000 claims abstract description 10
- 238000007765 extrusion coating Methods 0.000 claims abstract description 8
- 239000000758 substrate Substances 0.000 claims abstract description 8
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 7
- 230000001476 alcoholic effect Effects 0.000 claims abstract description 4
- 238000001125 extrusion Methods 0.000 claims abstract description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 21
- 239000005977 Ethylene Substances 0.000 claims description 21
- 239000005030 aluminium foil Substances 0.000 claims description 13
- -1 poly(ethylene/acrylic acid) Polymers 0.000 claims description 13
- 229920000642 polymer Polymers 0.000 claims description 12
- 229910052751 metal Inorganic materials 0.000 claims description 11
- 239000002184 metal Substances 0.000 claims description 11
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 8
- 239000004411 aluminium Substances 0.000 claims description 5
- 125000004185 ester group Chemical group 0.000 claims description 5
- 229920000554 ionomer Polymers 0.000 claims description 5
- 239000000155 melt Substances 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- 229910052723 transition metal Inorganic materials 0.000 claims description 5
- 150000003624 transition metals Chemical class 0.000 claims description 5
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 4
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- 239000000551 dentifrice Substances 0.000 claims description 4
- 229920005989 resin Polymers 0.000 claims description 4
- 239000011347 resin Substances 0.000 claims description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 3
- 239000004075 cariostatic agent Substances 0.000 claims description 3
- 229920001903 high density polyethylene Polymers 0.000 claims description 3
- 239000004700 high-density polyethylene Substances 0.000 claims description 3
- 238000007789 sealing Methods 0.000 claims description 3
- 238000001816 cooling Methods 0.000 claims description 2
- 238000000151 deposition Methods 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims 1
- JOGHZZBEPNPQNA-UHFFFAOYSA-N chromium;prop-2-enoic acid Chemical compound [Cr].OC(=O)C=C JOGHZZBEPNPQNA-UHFFFAOYSA-N 0.000 claims 1
- 229920001038 ethylene copolymer Polymers 0.000 abstract description 5
- 239000007864 aqueous solution Substances 0.000 abstract description 2
- 238000001035 drying Methods 0.000 abstract description 2
- 150000007942 carboxylates Chemical group 0.000 abstract 1
- 150000001735 carboxylic acids Chemical class 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 239000000047 product Substances 0.000 description 29
- 239000010410 layer Substances 0.000 description 23
- 239000002987 primer (paints) Substances 0.000 description 20
- 229920006226 ethylene-acrylic acid Polymers 0.000 description 16
- 239000004698 Polyethylene Substances 0.000 description 8
- 229920000573 polyethylene Polymers 0.000 description 8
- 238000003860 storage Methods 0.000 description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 6
- 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
- 239000000606 toothpaste Substances 0.000 description 6
- 229940034610 toothpaste Drugs 0.000 description 6
- 230000032798 delamination Effects 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- 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
- 239000000178 monomer Substances 0.000 description 3
- 239000000123 paper Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229940077232 absorbine Drugs 0.000 description 2
- 239000008330 absorbine Substances 0.000 description 2
- 125000005396 acrylic acid ester group Chemical group 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 230000006353 environmental stress Effects 0.000 description 2
- 239000013615 primer Substances 0.000 description 2
- 230000037452 priming Effects 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
- 239000000341 volatile oil Substances 0.000 description 2
- 241000207199 Citrus Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920003182 Surlyn® Polymers 0.000 description 1
- 241000270666 Testudines Species 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 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
- 235000020971 citrus fruits Nutrition 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
- 150000002148 esters Chemical class 0.000 description 1
- QHZOMAXECYYXGP-UHFFFAOYSA-N ethene;prop-2-enoic acid Chemical compound C=C.OC(=O)C=C QHZOMAXECYYXGP-UHFFFAOYSA-N 0.000 description 1
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 238000010030 laminating Methods 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
- 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
- 229920005672 polyolefin resin 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
- 238000009736 wetting Methods 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)
Abstract
PURPOSE: To allow a degenerative product to be stored in a package for a long time by forming a container of an aluminum foil, an ethylene copolymer film and a laminate web therebetween comprising polyacrylic acid chromium complex primer and placing the film on the product side in the container. CONSTITUTION: Polyacrylic acid chromium complex primer of a monomolecular layer blended as alcoholic aqueous solution is deposited on a face of an aluminum foil substrate for coating. The coated foil is heated for substantially drying the primer, thereafter an ethylene copolymer film is extrusion-coated onto a surface coated with the primer, and a formed laminate is cooled to finish a web. Preferably, a temperature of copolymer melt is approximately 288 to 316 deg.C during the extrusion-coating process. Then a container is formed with the laminate web disposed on a product side of the film container. The ethylene copolymer has carboxylic acid or a carboxylate group as a side chain.
Description
The present invention relates to laminate webs incorporating a polyacrylic acid complex primer, their applications and method of manufacture, containers ®r packages made therefrom and a method of making said containers or packages.
Tubes and other containers made of laminated webs, that are 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. American Can Company, of Greenwich, Connecticut, markets such tubular containers cnder its GLAMINATE trademark. By properly designing and constructing the laminate, oxygen and moisture barrier properties necessary for the containment cf many commodities are obtained, as are the heat sealability and dead fold characteristics that are desirable in a tube-like package. Typically, (die product side of the laminate web will comprise an olefinic polymer, 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 aluminium foil. SURLYN is a Trade Mark.
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 toothpaste to permeate the inner plastic layer, and to migrate to the metal interface, thereby promoting delamination in the web structure and causing deterioration of the contained product. Of course, the longer the period ofstorage the more pronounced will be the tendency for degeneration to occur in the laminate web, and particularly so if the package is stored at a relatively elevated temperature.
Various measures have been 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 is seen to significantly enhance bond strength, still it is not entirely satisfactory on long-term storage. The use of polyethylene as the product-facing 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 laminate web, suitable for making containers and packages, and comprised of aluminium 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.
According to the present invention, there is provided a laminate web suitable for use in producing containers for degenerative products, which includes metal e.g. aluminium foil, a film of a copolymer of ethylene having in its molecule pendant carboxylic acid or ester groups laminated to tjae foil, and at least a moncmolecular layer of a polyacrylic acid transition metal catplex primer being disposed at the interface between the foil and the film.
Also according to the present invention, there is provided 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 surface of a metal, e.g. aluminium,foil substrate at least a monomolecular layer of a polyacrylic acid transition metal complex primer from an aqueous alcoholic solution, heating the thus-coated substrate to substantially dry the primer; extrusion coating a film of a copolymer of ethylene upon the primed surface, or upon at least one of the primed surfaces, of the foil, the copolymer having pendant carboxcylic acid or ester groups
5413-1 in its molecule; and cooling the laminate to provide the web.
The primary object of the invention is readily attained by laminating the ethylenic copolymer to aluminium foil, preferably employing as the primer a polyacrylic acid chromium complex primer. 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/methacrylic acid), poly(ethylene/ methylacrylate), poly(ethylene/methyl methacrylate), poly(ethylene/vinyl acetate), and ionomer resins.
The primer coating can be significantly thicker than a monomolecular layer. 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.
To make the web, 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 aluminium foil substrate. The coated substrate is thereafter heated substantially to dry the primer. Following this, a film of a copolymer of ethylene (as described above) is extrusion coated upon the primed surface, preferably using the copolymer melt at a temperature of 550° to 600° Fahrenheit (288 to 310°C), and most desirably at a temperature of 575° to 590°
Fahrenheit (301° to 3l6°C).
A container for a degenerative product fabricated from the laminate web will have the copolymer film disposed on the product side thereof. The container may be a toothpaste tube filled with a degenerative dentrifice substance containing a fluoride anticaries agent and/or one or more essential oils. The container may thus be in the form of a tube having a headpiece bonded within one end of the tubular structure; the headpiece generally being made of a polyolefin resin, such as high density polyethylene.
The Invention will now be described in more detail by way of example only.
As noted initially, foil/ethylene copolymer laminate webs have previously been used in fabricating containers. The present invention provides means by which the strength of the bond between the foil and a copolymer layer on the product side is greatly enhanced, and is rendered substantially lass susceptible to degenerative ingredients that may migrate to the interface.
The chrome complexes that are utilized to prime the aluminium 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 (10 mPa s). The MICA A-291 product literature indicates use for bonding polyethylene to aluminium foil, for packaging and industrial applications requiring high bonds and resistance to a variety of hard-to-hold materials, including fluorides and essential oils. 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 present invention, i.e., the development of extremely durable bonds between aluminium 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
413 4 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, for example, cobalt, copper and nickel, might be substituted for chromium.
As indicated above, the primer will generally be applied as a dilute water/alcohol solution , to maximize leveling and wetting of the substrate, and thereby afford optimal levels of adhesion of the polymer layer thereto. To prepare the working liquid, the commercial MICA A-291 product may suitably be mixed with additional water and isopropyl alcohol in a volumetric ratio of 30: 60: 10 (product to water to alcohol).
The resulting solution will be used in an amount sufficient to provide, when dried, about 0.03 to 0.08, and preferably about 0.035, pound of complex solids per ream (i.e., 3,000 square feet of surface area), (48.8 g/1000 m^· 130 g/1000 and
57.0 g/1000 m^). In any event, the primer must
5413-1 be of at least monomolecular thickness, and generally it will be at least somewhat 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 or 121° to 204°C), the web may be presented directly to a copolymer extrusion station Then, its temperature will generally be about 100° to 150° Fahrenheit (38° to 66°C).
The techniques utilized for extrusion coating of the ethylene copolymer upon the aluminium 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 according to the invention will find their widest utility in the production of tubular containers, for which applications the web must be capable of side seaming and secure
413 4 attachment to a 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), as an example ethylene acrylic acid (EAA) will generally be extruded, in the practice of the present method, at a temperature of 550° to 600° Fahrenheit (288° to 316°C), An optimum balance of bonding properties will usually be realized with a melt temperature of about 575° to 590° Fahrenheit (302° to 310°C).
While EAA or ionomer will usually constitute the layer of the laminate web ultimately destined to face the product, 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 technique normally used to produce the foil/copolymer composite will be extrusion coating in view of its recognized economic and practical benefits.
However, other techniques may be found to be
413 4
IS feasible under certain circumstances, and may be employed if so desired. Generally, the thickness of the product-facing polymer will range from about 1.0 to 4.0 mils (0.02 to 0.10 mm), and more commonly 1.5 to 3.0 mils (0.04 to 0.03 mm) to provide an optimal functional and economic balance.
Insofar as the foil component is concerned, as a practical matter thin-gauge (i.e., about 0.265 to 3.0 mils or 0.007 to 0.08 mm) aluminium will normally be utilized, although for certain applications foils of other metals might be substituted. The laminate web will 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 arrangement will comprise (from the outside in) : polyethylene, paper, polyethylene, EAA, foil, primer, and lastly the EAA layer destined to face the product.
Save for the foil, primer, EAA subcombination, the basic structure is conventional.
The manner in which the laminate web is converted into a container tube (e.g., head bonding, side seaming, and end sealing to form and close the tube) may be entirely conventional and known to those skilled in the art. Accordingly, a detailed description is unnecessary. It might be mentioned, however, that in forming the side seam it is common practice to overlap 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 the following specific examples:
EXAMPLE ONE
Webs are produced, utilizing a laminate subassembly comprised of layers of polymers and paper bonded to one face of 0.7 mil (0.016 mm) thick aluminium foil, the overall gauge of the subassembly being about 10.2 mils (0.26 mm). 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 50: 60: 10 solution of MICA A-291: water: isopropyl alcohol, which is subsequently forced air dried in an oven, at about 250° Fahrenheit (121°C).
A first laminate is produced by extrusion coating the primed, foil surface with 43.5 pounds per ream (70.8 kg/m ) of low density polyethylene, the extrudate being at a temperature of about 600° Fahrenheit (316°C). This laminate is designated
A. A second laminate, designated BM, 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 (316°C). A third laminate designated 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 (2.54 x
14.3 cm), which are filled 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 (24° and 41°C), and three pillows of each sample are held at a temperature of 120° Fahrenheit (49°C). They are evaluated at intervals of two, four, eight, twelve, and twenty-six weeks. The results are set forth in Table One, which follows:
ILE ONE
CM rt
o CM rH • I 1 O rt fa J, 0 Cn 3 in *? 0 0 ci o CM rt 1 1 1 8 H fa ci ci lA ί ί 0 0 ci O CM *? H fa fa 0 8 rt fa 3 3 in *? *? n- 0 ci ci o CM rt fa ra • I ra 3 m (3 *T o O Cx ft rt m b- 1 1 1 o CM 0 1 «? rt 0 ci in O rt 1 1 1 in b- I 1 1
Cn
O
Φ h
·£
S
0) §· «<
ra υ
41 3 J
As used in the Table, the designations E,
G, F and MPH, 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 polymer layer becomes stretched in endeavoring to separate it from 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 MBn 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 (49°C), and 8 or 12 weeks at 105° Fahrenheit (41°C), 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
4.13 4 as reflected in Table One, it can b.e 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 (4l°C),the pillows produced from the polyethylene web are found to be highly prone to cracking when 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 aluminium foil, the polymer and foil gauges being 2.0 and 0.352 mil (0.051 and 0.008 mm), 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. Ihe pouches are sealed and stored at a temperature of 105°
Fahrenheit (41°C), 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 month, the webs made with the primed aluminium show good adhesion regardless of whether the polymer layer is comprised of EAA or ionomer. The unprimed aluminium, on the other hand, produces webs in which delamination (in the case of EAA) or poor adhesion (in the case of the ionomer) occurs. The results are the same following the two-months storage period.
Although, the foregoing specific examples demonstrate the outstanding ability of the present 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 webs can be used advantageously for packaging a wide range of other products deemed to be difficult to contain. For example, the web according to the Invention can successfully survive the degenerative effects of NOXEMA Brushless Shave Cream (Noxell Corporation); Helena Rubenstein Skin Lightener; Dap, Inc. Waterless Hand Cleaner; VAGINEX Cream (Schmid Laboratories);
Plymouth Citrus Products Industrial Waterless Hand Cleaner; TURTLE WAX Auto Polish Glaze;
ARTRA. Skin Tone Cream (Plough Inc.); Union Carbide Corporation car polish; ABSORBINE RUB (W.F. Young,
Inc.); Red Glazing Putty (Oatey Co.); IX 845 Auto Glaze (Petrolite Corporation), and Soupletuhe (France) Product No. 3· In all instances the degree of resistance to delamination is at a very good level, but the specific results achieved with any particular product will, of course, vary. Moreover, it will be appreciated that the foregoing list of commercial products is intended only to he exemplary, and that the laminate webs made in accordance with the present invention may be utilized with comparable advantage for many other products.
Thus, it can be seen that the present invention provides a novel laminate web comprised of aluminium foil and a layer of a copolymer of ethylene with an acrylic acid or acrylic acid ester monomer, which web is adapted for successfully containing degenerative products for extended periods of time. The invention also provides a novel container and package fabricated from such a laminate web, and novel methods for the production of such webs, containers and packages.
DUCO, NOXEMA, VAGINEX, TURTLE WAX, ARTRA, ABSORBINE RUB, AUTO GLAZE and SOUPLE-TUBE are Trade Marks.
Claims (19)
1. A laminate web suitable for use in producing containers for degenerative products, which includes metal foil, a film of a copolymer of ethylene having in its molecule pendant carboxylic acid or ester groups laminated to the foil, and at least a monomolecular layer of a polyacrylic acid transition metal complex primer being disposed at the interface between the foil and the film.
2. A web according to claim 1, wherein the metal foil is aluminium foil.
3. A web according to claim 1 or 2, wherein the copolymer is selected from poly(ethylene/acrylic acid), poly(ethylene/methacrylic acid), poly(ethylene/methyl acrylate), poly(ethylene/methyl methacrylate), poly(ethylene/vinyl acetate), and ionomer resins.
4. A web according to any one of claims l to 3, additionally including a film of a synthetic resinous polymer on the side of the foil opposite to the primer.
5. A web according to any preceding claim, wherein the primer comprises a polyacrylic acid chromium complex.
6. A web according to any preceding claim, wherein the primer is present in an amount of 48.8 to 130 g/1000 m of web, the copolymer film is 0.02 to 0.10 mm thick and the foil is 0.007 to 0.08 mm thick. •54134 1. A laminate web according to claim 1 and substantially as herein described by way of example.
7. 8. A container for a degenerative product fabricated from the laminate web claimed in any 5 of claims 1 to 7, wherein the said copolymer Ή1m is on the product-facing side thereof.
8. 9. A container according to claim 8, wherein the laminate web is formed into a tubular configuration, and a headpiece is secured to one
9. 10 end of the tubular structure. 10. a container according to claim 9, wherein the headpiece is fabricated from high density polyethylene.
10. 11. a container according to claim 5 15 or io, wherein the laminate is formed into a side-seamed tube by heat sealing and the headpiece is heat sealed thereto.
11. 12. A package comprised of the container claimed in any of claims 8 to ll, and a degenerative 20 product contained therein.
12. 13. A package according to claim 12 , wherein the said product is a dentifrice substance containing a fluoride anticaries agent. 14 . A method for the production of a 25 laminate web suitable for use in producing containers S4134 S3 for degenerative products, the steps including: depositing upon at least one surface of a metal e.g, aluminium, foil substrate at least a monomolecular layer of a polyacrylic acid transition metal complex primer from an aqueous alcoholic solution, heating the thus-coated substrate to substantially dry the primer; extrusion coating a film of a copolymer of ethylene upon the primed surface, or upon at least one of the primed surfaces, of the foil, the copolymer having pendant carboxcylic acid or ester groups in its molecule; and cooling the laminate to provide the web.
13. 15 . A method according to claim 14, wherein the copolymer is selected from poly(ethylene/ acrylic acid) poly(ethylene/methacrylic acid) poly(ethylene/methyl acrylate), poly(ethylene/ methyl methacrylate), poly(ethylene/vinyl acetate) and ionomer resins.
14. 16, A method according to claim 15, wherein the copolymer is poly(ethylene/acrylic acid), and wherein said copolymer is extruded from an extrusion dye at a melt temperature of 550° to 600° Fahrenheit (232 to 316°C).
15. 17 . a method according to claim i£*, wherein the melt temperature is 575° to 590° Fahrenheit (302 to 310°C).
16. 18. a method according to any of claims 14 to 17 wherein the foil is coated with a poly5 acrylic acid chromium complex primer.
17. 19. A method according to any of claims 14 to 18, wherein the web is formed into a container configuration with said copolymer film disposed on the inside thereof. 10 20 . A method according to claim 19, wherein the web is formed into a tubular structure, and wherein a headpiece is bonded to said web at one end of the resulting tubular structure. 21. a method according to claim 20, 15 wherein the headpiece is fabricated from high density polyethylene. 22. A packaging method comprising the steps of forming the container as claimed in claim 19,
18. 20 or 21 and filling the container with a 20 degenerative product such as a dentifrice substance containing a fluoride anticarles agent.
19. 23. A method according to claim 14 of making a laminate web and substantially as herein described by way of example.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US34046882A | 1982-01-18 | 1982-01-18 |
Publications (2)
Publication Number | Publication Date |
---|---|
IE830079L IE830079L (en) | 1983-07-18 |
IE54134B1 true IE54134B1 (en) | 1989-06-21 |
Family
ID=23333479
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IE79/83A IE54134B1 (en) | 1982-01-18 | 1983-01-17 | Laminates incorporating a polyacrylic acid caomplex primer, packaging or containers made therefrom and manufacture of said laminates |
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 PT PT76096A patent/PT76096B/en unknown
- 1983-01-17 IE IE79/83A patent/IE54134B1/en not_active IP Right Cessation
- 1983-01-17 PH PH28625A patent/PH20707A/en unknown
- 1983-01-17 BR BR8300184A patent/BR8300184A/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 |
---|---|
MX163612B (en) | 1992-06-05 |
NO830112L (en) | 1983-07-19 |
BR8300184A (en) | 1983-10-11 |
PT76096A (en) | 1983-02-01 |
NZ202957A (en) | 1986-03-14 |
JPH0555380B2 (en) | 1993-08-16 |
JPS58124642A (en) | 1983-07-25 |
IE830079L (en) | 1983-07-18 |
JPH0259056B2 (en) | 1990-12-11 |
DK162753B (en) | 1991-12-09 |
AR240951A1 (en) | 1991-03-27 |
KR900004782B1 (en) | 1990-07-05 |
AR240951A2 (en) | 1991-03-27 |
IN159631B (en) | 1987-05-30 |
PT76096B (en) | 1986-03-18 |
DK162753C (en) | 1992-04-27 |
ZA829458B (en) | 1984-02-29 |
GR77880B (en) | 1984-09-25 |
CA1201050A (en) | 1986-02-25 |
PH20707A (en) | 1987-03-30 |
DK18983D0 (en) | 1983-01-18 |
ES8502904A1 (en) | 1985-02-01 |
KR840003069A (en) | 1984-08-13 |
DK18983A (en) | 1983-07-19 |
JPH03646A (en) | 1991-01-07 |
MX9100155A (en) | 1993-01-01 |
IN162390B (en) | 1988-05-21 |
ES530166A0 (en) | 1985-02-01 |
NO161965C (en) | 1989-10-18 |
IL67555A (en) | 1988-03-31 |
NO161965B (en) | 1989-07-10 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM4A | Patent lapsed |