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
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
• • 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
  • B32B15/00—Layered products comprising a layer of metal
  • B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
  • B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
• • 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
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
  • B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
• • 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
  • B32B27/00—Layered products comprising a layer of synthetic resin
• • 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
  • B32B38/00—Ancillary operations in connection with laminating processes
  • B32B38/0008—Electrical discharge treatment, e.g. corona, plasma treatment; wave energy or particle radiation
• • 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
  • B32B2255/00—Coating on the layer surface
  • B32B2255/10—Coating on the layer surface on synthetic resin layer or on natural or synthetic rubber layer
• • 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
  • B32B2255/00—Coating on the layer surface
  • B32B2255/20—Inorganic coating
  • B32B2255/205—Metallic coating
• • 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
  • B32B2310/00—Treatment by energy or chemical effects
  • B32B2310/14—Corona, ionisation, electrical discharge, plasma treatment
• • 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
  • B32B2323/00—Polyalkenes
  • B32B2323/04—Polyethylene
  • B32B2323/043—HDPE, i.e. high density polyethylene
• • 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
  • B32B2323/00—Polyalkenes
  • B32B2323/10—Polypropylene
• • 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
  • B32B2439/00—Containers; Receptacles
• • Y—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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
  • Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
  • Y10T428/24851—Intermediate layer is discontinuous or differential
  • Y10T428/24868—Translucent outer layer
• • Y—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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
  • Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
  • Y10T428/24917—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.] including metal layer
• • Y—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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
  • Y10T428/24942—Structurally defined web or sheet [e.g., overall dimension, etc.] including components having same physical characteristic in differing degree
  • Y10T428/2495—Thickness [relative or absolute]
• • Y—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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31—Surface property or characteristic of web, sheet or block
• • Y—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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31678—Of metal
  • Y10T428/31692—Next to addition polymer from unsaturated monomers
• • Y—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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31855—Of addition polymer from unsaturated monomers
  • Y10T428/31909—Next to second addition polymer from unsaturated monomers
• • Y—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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31855—Of addition polymer from unsaturated monomers
  • Y10T428/31909—Next to second addition polymer from unsaturated monomers
  • Y10T428/31913—Monoolefin polymer
• • Y—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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31855—Of addition polymer from unsaturated monomers
  • Y10T428/31935—Ester, halide or nitrile of addition polymer

Definitions

• U.S. Patent No. 4,345,005 discloses oriented polypropylene film having enhanced adhesion to metallized coatings produced by coextruding a film substrate having a polypropylene homopolymer core layer and a propylene- ethylene copolymer outer layer, biaxially orienting the film, and corona discharge treating the outer layer. A metal coating may then be deposited on the corona discharge treated layer.
• U.S. Patent No. 4,692,380 discloses metallized biaxially oriented polypropylene films produced by coextruding polypropylene homopolymer containing a fatty acid amide slip agent as the core layer with a propylene- ethylene copolymer which forms a thin layer on one surface of the polypropylene core layer, subjecting the propylene- ethylene layer to a corona discharge treatment, and metallizing the corona-discharge treated surface.
• U.S. Patent No. 5,126,198 discloses heat-laminatable multilayer films comprising a polypropylene base layer and at least one additional layer containing a mixture of an ethylene/ vinyl acetate copolymer and an ethylene/acrylic acid copolymer.
• a metallized multilayer film suitable for packaging applications comprising a film substrate having in cross-section a polymer core layer, on at least one surface of which is a skin layer of a polymer having a lower melting temperature than the polymer of the core layer, the exposed surface of such skin layer having been treated, e.g., flame or corona discharge treated, prior to coating to increase its adherence to other materials, such film substrate containing a metal layer, e.g., of aluminum, deposited on said treated skin layer surface and a low temperature sealable coating (LTSC) comprising a copolymer of 10 to 35 wt.% of an alpha, beta-ethylenically unsaturated carboxylic acid with 65 to 90 wt.% of ethylene, an alkyl acrylate or methacrylate, acrylonitrile or a mixture thereof, deposited directly, i.e., without a primer, on the exposed surface of the metal layer.
• LTSC low temperature sealable coating
• the film of this invention is suitable for packaging applications where the metal layer is protected from damage by a sealable coating with good metal adhesion and high seal strength.
• the polymer of the core layer of the film of this invention generally has mechanical properties considered necessary or desirable in the film.
• such polymer is a polyolefin having a melting point, for example, of at least 125°C and up to for example, 190°C, and a relatively high degree of crystallinity.
• a particularly desirable polyolefin making up the core layer is an isotactic polypropylene homopolymer which is, for example, 93 to 99% isotactic and has a crystallinity of 70 to 80%, and a melting point, for example, of 145°C or higher, e.g. , up to 167°C.
• HDPE high density polyethy ⁇ lene
• microspheres may optionally be dispersed in the core layer polymer before extrusion and orientation of the film.
• Such microspheres are composed of a material higher melting than and immiscible with the core layer polymer and may be any of those disclosed, for example, in U.S. Patent Nos. 4,377,616 and 4,632,869.
• the microspheres may be composed of a polymer, e.g.
• microspheres a polyester such as a polybutylene terephthalate (PBT) or polyethylene terephthalate (PET) , a nylon, an acrylic resin, or polystyrene, or an inorganic material such as glass, metal or ceramic.
• PBT polybutylene terephthalate
• PET polyethylene terephthalate
• the preferred material for the microspheres is PBT.
• the particle size of the microspheres may be, for example, 0.1 to 10 microns, preferably 0.75 to 2 microns.
• the microspheres may be present in the core layer in an amount of up to 20 wt.%, preferably 6 to 12 wt.% based on the total weight of the core layer.
• a thin layer of core layer polymer in the absence of microspheres may be coextruded on one or both sides of the microsphere-containing core layer polymer.
• the total of the microsphere- containing polymer layer and the non-microsphere-containing polymer layers may be considered the overall core layer of the film on each side of which is an adjacent skin layer having a greater adhesiveness to other materials than the core layer.
• the polymer of the skin layer adjacent to one or both surfaces of the core layer is preferably an extrudable hydrocarbon polymer such as a polyolefin having a lower melting point, e.g. , at least 5°C lower and up to 50°C lower, than the polymer of the core layer.
• Suitable polymers include isotactic polypropylene homopolymer, isotactic copolymers of propylene and a minor amount, e.g., 1 to 10 wt.%, of one or more different 1-olefins, e.g., ethylene or a higher 1-olefin having, for example 4 to 8 carbons atoms.
• Other polymers which can be used for the skin layers of the film substrate when the core layer polymer is an isotactic polypropylene homopolymer are, for example, high density polyethylene (HDPE) , and linear low density polyethylene (LLDPE) .
• HDPE high density polyethylene
• LLDPE linear low density polyethylene
• the polymer of the skin layers adjacent to the core layer may be any of the polymers disclosed previously except for HDPE itself, as long as the polymer has a lower melting point than the HDPE making up the core layer.
• the polymers of the skin layers may be the same or different.
• the film is usually prepared by coextruding the polymers of these layers. After such extrusion of the basic film substrate utilizing conventional extrusion techniques, the film is heated and molecularly oriented in the longitudinal, i.e., machine, direction and optionally in the transverse direction.
• This uniaxial or biaxial orientation which greatly improves the stiffness and tensile strength properties of the film, is accomplished by utilizing conventional techniques to stretch sequentially the film, for example, three to eight times in the machine direction and optionally, five to twelve times in the transverse direction, at a drawing temperature of 100° to 200°C.
• a coextruded film having a core layer of polypropylene homopolymer would be biaxially oriented, while a film having a core layer of LDPE would be uniaxially oriented, i.e., only in the machine direction.
• the final polymer substrate is essentially unoriented and the final metallized film is generally much less stiff than films in which the substrate is prepared by a coextrusion and orientation process.
• the surfaces intended to receive the metal coating and optionally the opposite surface are treated to insure that the coatings will be strongly adherent to the film substrate, thereby eliminating the possibility of the coatings peeling or being stripped from the film.
• This treatment can be accomplished by employing known prior art techniques such as for example, film chlorination, i.e., exposure of the film to gaseous chlorine, treatment with oxidizing agents such as chromic acid, hot air or steam treatment, flame treatment, corona discharge treatment, and the like. Flame or corona discharge treatment of the surfaces is typical in the production of the films of this invention.
• a metal layer to a treated surface of the film substrate is usually accomplished by conventional vacuum deposition although other methods known in the art such as electroplating or sputtering may also be used.
• Aluminum is preferred as the metal utilized for this purpose although other metals similarly capable of being deposited such as gold, zinc, copper, silver and others known in the art may also be utilized for certain purposes.
• the unsaturated carboxylic acid may be, for example, acrylic acid, methacrylic acid, maleic acid, crotonic acid, itaconic acid, citraconic acid, or mixtures thereof.
• the copolymer is a copolymer of 65 to 90 wt.%, more usually 75 to 85 wt.% of ethylene, and 10 to 35 wt.%, usually 15 to 25 wt.% of acrylic acid (an EAA copolymer) or methacrylic acid (an EMA copolymer) .
• the copolymer may have a number average molecular weight (Mn) of, for example, 2,000 to 50,000, preferably 4,000 to 10,000.
• the carboxylic acid copolymer in the low temperature sealable coating applied to the metallized surface is often obtained as a solution or fine dispersion of an ammonium salt of the copolymer in an ammoniacal water solution.
• ammonia is given off and the ionized and water sensitive carboxylate groups are converted to largely unionized and less water sensitive free carboxyl groups.
• the quantity of such metallic ions may be in the range sufficient to neutralize, for example, 2 to 80%, preferably 10 to 50% of the total carboxylate groups in the copolymer.
• the presence of such metallic ions has been found in many cases to result in an improvement in certain properties, e.g., coefficient of friction (COF) , hot tack, and blocking, without an unacceptable sacrifice of other properties, e.g., low minimum seal temperatures (MST) .
• the amount of sodium hydroxide added corresponding to the foregoing percentages of carboxylate groups neutralized may be, for example, 0.33 to 8.8 phr, preferably 1.1 to 5.5 phr, where "phr" stands for parts by weight per hundred parts of the total resin, which is the same as the EAA copolymer when no other resin is present.
• phr stands for parts by weight per hundred parts of the total resin, which is the same as the EAA copolymer when no other resin is present.
• all the carboxylate groups of the ethylene copolymer are assumed to be in their free carboxyl (-C00H) form.
• the sealable coating applied to the metallized surface may also contain a dispersed wax, e.g. , a relatively large particle size carnauba or microcrystalline wax as an anti-blocking agent.
• a dispersed wax e.g. , a relatively large particle size carnauba or microcrystalline wax as an anti-blocking agent.
• Other waxes which may be used are, for example, natural waxes such as paraffin wax, beeswax, japan wax, montan wax, etc., and synthetic waxes such as hydrogenated castor oil, chlorinated hydrocarbon waxes, long chain fatty acid amides, etc.
• the wax may be present in the coating in an amount of, for example, 2 to 12 phr, preferably 3 to 5 phr.
• the wax when incorporated into the coatings of the present invention also functions to improve the "cold- slip" properties of the films coated therewith, i.e., the ability of a film to satisfactorily slide across surfaces at room temperature.
• the sealable coating applied to the metallized surface of the film may also contain a particulate material, e.g., an amorphous silica, for the purpose of further reducing the tack of the coating at room temperature.
• Amorphous silica is composed of particles which are agglomerations of smaller particles and which have an average particle size of, for example, 2 to 9 microns, preferably 3 to 5 microns, and may be present in the sealable coating in an amount, for example, of 0.1 to 2.0 phr, preferably 0.2 to 0.4 phr.
• additives which may be included in the sealable coating applied to the metallized surface of the film include other particulate materials such as talc which may be present in an amount, for example, of 0 to 2 phr, cross-linking agents such as melamine formaldehyde resins which may be present in an amount, for example, of 0 to 20 phr, and anti-static agents such as poly(oxyethylene) sorbitan monooleate which may be present in an amount, for example, of 0 to 6 phr.
• An anti-bacterial agent may also be present.
• a polymeric, film-forming coating may optionally be applied to the surface of the film opposite the metallized surface.
• a coating of primer is first applied to such surface, either after the skin layer on such surface is treated to increase further its adhesiveness to other materials or in the absence of such treatment.
• Primer materials which are suitable are well known in the art and include, for example, titanates, poly(ethyleneimine) , and reaction products of an epoxy resin and an aminoethylated vinyl polymer. The primer is applied to the treated surface of the film substrate by conventional solution coating means.
• a particularly effective primer herein is poly(ethylene imine) applied as either an aqueous or organic solvent e.g., ethanol, solution, or as a solution in a mixture of water and organic solvent, containing 0.5 wt.% of the imine.
• an aqueous or organic solvent e.g., ethanol, solution, or as a solution in a mixture of water and organic solvent, containing 0.5 wt.% of the imine.
• the coating applied to the primer-containing surface of the film opposite the metallized surface may be a sealable coating of the same type as that applied to the metallized surface or it may be any of other types of polymeric, film-forming coatings known in the art.
• a particularly suitable coating is one containing as a film- forming component an interpolymer of 1) 18 to 80 wt.% of at least one alkyl methacrylate, 2) 18 to 80 wt.% of at least one C ⁇ -C 4 alkyl acrylate, and 3) 1 to 15 wt.% of at least one alpha, beta-ethylenically unsaturated carboxylic acid based on the weight of the polymer (an "acrylic terpolymer”) ; and colloidal silica as a hot slip agent in an amount, for example of 30 to 60 phr and having a particle size of, for example, 10 to 200 millimicrons.
• the unsaturated acid of the acrylic terpolymer may be any of those disclosed previously as suitable for the copolymer in the low temperature sealable coating applied to the metallized surface of the film, although acrylic and/or methacrylic acid are preferred.
• the copolymer may be utilized in the coating composition as a partially neutralized aqueous solution or as a dispersion, i.e., a latex.
• Additives may be present in the coating compositions which are the same or similar in nature and amount as those disclosed previously as suitable in the low temperature sealable coating applied to the metallized surface of the film, particularly a wax such as carnauba wax which functions as an antiblocking and cold slip agent, and talc which acts as a lubricant.
• composition is disclosed, for example, in U.S. Patents Nos. 3,753,769 and 4,749,616.
• Another type of polymeric coating which may be applied to the surface of the film opposite the metallized surface in conjunction with a primer is a coating in which the film-forming component is a polymer of at least 50 wt.% of vinylidine chloride, preferably 75 to 92 wt.% of vinylidine chloride, 2 to 6 wt.% of an alpha, beta-ethylenically unsaturated acid such as any of those disclosed previously as suitable for the copolymers in sealable coatings and the remainder a Ci-C 4 alkyl acrylate or methacrylate, or acrylonitrile.
• the vinylidine chloride copolymer may be utilized as a partially neutralized aqueous solution or as an aqueous dispersion, i.e., a latex. This type of coating is disclosed, for example, in U.S. Patent No. 4,944,990.
• the contemplated low temperature sealable coating (LTSC) composition is applied to the metallized surface of the polymer film, and, if used, the primer and polymeric coatings to the opposite surface, in any suitable manner such as by gravure coating, roll coating, dipping, spraying, etc.
• the excess aqueous solution can be removed by squeeze rolls, doctor knives, etc.
• the coating compositions will ordinarily be applied in such an amount that there will be deposited following drying, a smooth, evenly distributed layer of from 0.2 to 1 gram/1000 sq. in. of film surface.
• the thickness of the applied LTSC is such that it is sufficient to impart the desired sealability, coefficient of friction (COF) , and hot slip characteristics to the substrate polymer film.
• the coating once applied to the film is subsequently dried by hot air, radiant heat or by any other suitable means thereby providing a non-water soluble, adherent, glossy coated film product useful, for example, as a packaging film.
• a printed ink pattern may be applied to the coating on either surface of the film, or to the uncoated surface opposite the metallized surface if no coating is applied to such opposite surface, using, for example a conventional solvent-based ink composition.
• the printed pattern may be covered with an overlacquer to prevent the pattern from damage.
• the overlacquer may cover the entire surface containing the printed pattern, in which case sealing is accomplished solely by the softening of the coating or a polymer skin layer on the opposite surface of the film on the portion of the film constituting the outer film of the seal.
• an "in to out” seal wherein sealing is also accomplished by the softening of the coating or polymer skin layer on the surface containing the printed ink pattern, a portion of which constitutes the inner film of the seal, then the printing and overlacquering is done in a pattern to allow the coating or polymer skin layer to be exposed in the sealing region.
• the laminating film may be laminated to a surface of the metallized film of this invention, to which an overlacquer has not been applied, for the purpose of improving the mechanical properties, e.g., tear strength, and machinability, increasing the stiffness, protecting the printed pattern and/or providing hermetic seals of the metallized film.
• the laminating film may be bonded to a sealable coating on either the metallized surface or the opposite surface of the film of this invention, either after a printed pattern has been applied to the sealable coating or in the absence of such printed pattern, or the bonding of the laminated film may be to said opposite surface in the absence of any sealable coating.
• the laminating film may, for example, comprise a polymer having superior mechanical properties, e.g., isotactic polypropylene homopolymer, which is bonded to the film of the invention using as an adhesive molten polymer having a lower melting point than the laminating polymer, e.g., low density polyethylene (LDPE), or the laminating film may comprise a major layer of such polymer of superior mechanical properties and a minor layer of a polymer having a lower melting temperature than the polymer of the major layer with the lamination being accomplished by pressing the surface of the laminating film containing such minor layer against the desired surface of the metallized film of the invention at a temperature high enough to render tacky the polymer of the minor layer.
• LDPE low density polyethylene
• EXAMPLE A three layer film is extruded with a core layer of an isotactic polypropylene homopolymer sold as Fina 3371, a coextruded skin layer of HDPE on one surface of the core layer, and a coextruded skin layer of an isotactic terpolymer of over 90 wt.% of propylene and 1-5 wt.% each of ethylene and butene-1, sold as Chisso 7780 on the other surface of the core layer.
• the HDPE skin layer was composed of 97.5 wt.% of a pure HDPE sold as Exxon HX0353.67, 0.5 wt.% of a fluoropolymer to prevent die build up sold as Huntsman Polcomm A27527, and 2.0 wt.% of a master batch of HDPE with high stabilizer to prevent gels.
• the coextrudate was quenched at 30° to -50°C, reheated to 115°C and stretched in the machine direction 5 times using transport rolls operating at different speeds. After the desired machine direction, the film was transversely stretch oriented 8 times, at an appropriate temperature profile ranging from 155° to 180°C.
• the resulting film substrate had an overall optical gauge thickness of 70 ga. (gauge, 1/100 mil) with a core layer of 62 ga. (layer B) , an HDPE skin layer of 2 ga., (layer A) and a propylene-ethylene-butene-1 terpolymer skin layer of 6 ga., (layer C) .
• the HDPE skin layer was flame treated and metallized by vacuum deposition of aluminum under standard conditions for high barrier aluminum metallizing to an optical density of 2.3.
• a sealable coating composition is prepared by adding to an aqueous solution or fine dispersion of 25 wt.% of an a ⁇ unonium salt of a copolymer of 80 wt.% of ethylene and 20 wt.% of acrylic acid, sold by Michelman as MichemPrime 4983 EAA, 1.5 phr (parts by weight per hundred parts of the copolymer) of sodium hydroxide (NaOH) , 4 phr of carnauba wax sold by Michelman as MichemLube 215, 0.4 phr of talc, and 0.3 phr of amorphous silica sold as Syloid 42.
• the coating composition was applied to the metallized surface of the film in the absence of a primer using standard gravure and coating apparatus and techniques, and the coating was dried at 240°F.
• the total coating weight on the film following drying was from 0.65 grara/1,000 in 2 of film.
• the untreated surface of the film substrate which is opposite the metallized surface and which contains a skin layer of a propylene-ethylene-butene-1 terpolymer was first primed with a 0.5 wt.% solution of poly(ethylene- imine) in a mixture of 85% water and 15% ethanol.
• the primed surface was then coated with a composition comprising an aqueous dispersion or solution of a terpolymer of methyl methacrylate, ethyl acrylate and methacrylic acid, colloidal silica, and carnauba wax, with a total solids content of 13 wt.%, as described in U.S. Patent No. 2,753,769, to a coating weight of 0.6 gm/1000 in 2 of film, using standard gravure coating apparatus and techniques and a drying temperature of 240°C.
• the coated film of this example was tested for Water Vapor Transmission Rate (WVTR) in g/100 in 2 /day measured at 100°F and 90% R.H. , Oxygen Transmission Rate (OTR) in cc/100in 2 /day measured at 73°F and 0% R.H. , Minimum Seal Temperature (MST) in degrees F to obtain lOOgm/in flat seal with metallized HDPE (A) layer, and the crimp seal strength (CRIMP) of the metallized HDPE (A) layer at 20 psi, 0.75 sec. and 260°F.
• WVTR Water Vapor Transmission Rate
• OTR Oxygen Transmission Rate
• MST Minimum Seal Temperature
• MST Minimum Seal Temperature
• CRIMP crimp seal strength

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• 1996
  • 1996-05-07 US US08/646,429 patent/US6013353A/en not_active Expired - Fee Related
• 1997
  • 1997-05-05 BR BR9710840-5A patent/BR9710840A/pt not_active Application Discontinuation
  • 1997-05-05 EP EP97925458A patent/EP0904196B1/en not_active Expired - Lifetime
  • 1997-05-05 JP JP09540124A patent/JP2000510060A/ja not_active Ceased
  • 1997-05-05 KR KR1019980708986A patent/KR20000010844A/ko not_active Withdrawn
  • 1997-05-05 DE DE69730028T patent/DE69730028T2/de not_active Expired - Fee Related
  • 1997-05-05 ES ES97925458T patent/ES2225972T3/es not_active Expired - Lifetime
  • 1997-05-05 AU AU30589/97A patent/AU708299B2/en not_active Ceased
  • 1997-05-05 CA CA002253808A patent/CA2253808A1/en not_active Abandoned
  • 1997-05-05 WO PCT/US1997/007586 patent/WO1997042028A1/en not_active Ceased
  • 1997-05-07 AR ARP970101898A patent/AR007037A1/es unknown
  • 1997-05-07 ID IDP971529A patent/ID16883A/id unknown

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