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
  • B32B27/06—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
  • 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
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
• • 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
  • B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
  • B32B7/04—Interconnection of layers
  • B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
  • C08F255/02—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having two or three carbon atoms
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
  • C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
  • C08L51/003—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
  • C08L51/06—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
  • C09D151/003—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
  • C09D151/06—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J123/00—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
  • C09J123/02—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
  • C09J123/04—Homopolymers or copolymers of ethene
  • C09J123/08—Copolymers of ethene
  • C09J123/0846—Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
  • C09J123/0869—Acids or derivatives thereof
  • C09J123/0884—Epoxide containing esters
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J151/00—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
  • C09J151/003—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J151/00—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
  • C09J151/06—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
• • 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
• • 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
  • B32B2367/00—Polyesters, e.g. PET, i.e. polyethylene terephthalate
• • 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
  • B32B2439/70—Food packaging
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
  • C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
• • 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]
  • Y10T428/31652—Of asbestos
  • Y10T428/31667—Next to addition polymer from unsaturated monomers, or aldehyde or ketone condensation product
• • 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]
  • Y10T428/31786—Of polyester [e.g., alkyd, etc.]
• • 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
  • Y10T428/31928—Ester, halide or nitrile of addition polymer

Definitions

• the present invention relates to a packaging material comprising a layer of silicon oxide and a layer of polyolefin.
• It relates more particularly to a structure comprising a film covered with silicon oxide and a polyolefin film, an adhesion binder being disposed between the silicon oxide and the polyolefin film.
• a structure comprising a film covered with silicon oxide and a polyolefin film, an adhesion binder being disposed between the silicon oxide and the polyolefin film.
• One can, for example, on the side of the polyolefin film hot paste this material on cardboard, then cover each side of the assembly obtained with a polyethylene sheet.
• JP 03099842 published on April 25, 1991 describes EVOH ⁇ / inyl silane films covered with silicon oxide onto which a polypropylene sheet is bonded using a urethane adhesive.
• JP 05330568 published on December 14, 1993 describes polyester films coated with silica onto which an ethylene resin sheet is glued using an adhesive which is an ethylene-maleic anhydride-ethyl acrylate copolymer.
• the present invention is a material comprising a film covered with silicon oxide and a polyolefin film, such that the binder placed between the silicon oxide and the polyolefin film is chosen from:
• the film covered with silicon oxide is known from the prior art. It is for example a polyester film such as polyethylene terephthalate (PET) or polybutylene terephthalate (PBT) or polyamide (PA).
• PET polyethylene terephthalate
• PBT polybutylene terephthalate
• PA polyamide
• the polyolefin film is made of polyethylene, polypropylene or ethylene copolymers such as for example ethylene-propylene, ethylene butene, ethylene hexene, ethylene - (meth) acrylate or ethylene-vinyl acetate copolymers.
• the polyolefins which are grafted with alkoxysilanes can be chosen from: - homopolymers of ethylene, or of propylene;
• alkyl (meth) acrylate - copolymers of ethylene and at least one alkyl (meth) acrylate.
• the alkyl group of alkyl (meth) acrylate has up to 10 carbon atoms and can be linear, branched or cyclic.
• alkyl (meth) acrylate there may be mentioned in particular n-butyl acrylate, methyl acrylate, isobutyl acrylate, 2-ethylhexyl acrylate, l cyclohexyl acrylate, methyl methacrylate, ethyl methacrylate.
• acrylates ethyl acrylate, methyl acrylate, n-butyl acrylate and methyl methacrylate are preferred.
• - copolymers of ethylene and an alphaolefin such as butene or hexene are preferred.
• APAO - amorphous polyalphaolefins
• the APAOs derived from ethylene, propylene, butene or hexene are used.
• ethylene propylene butene copolymers with a high butene content or ethylene propylene butene copolymers with a high propylene content or homo or copolymers of butene are used.
• ethylene / alkyl (meth) acrylate copolymers are used.
• CH 2 CR 1 - CO - O - Y - Si (OR) 3 the (meth) acryloxyalkyltrialcoxysilanes (or (meth) acrylsilanes) in which: R is an alkyl having from 1 to 5 carbon atoms or an alkoxyl - R 2 OR 3 in which R 2 and R 3 are alkyls having at most 5 carbon atoms for the whole R 2 and R 3 .
• Ri is hydrogen or methyl.
• Y is an alkylene having from 1 to 5 carbon atoms.
• vinylsilanes such as trimethoxyvinylsilane, triethloxyvinylsilane, triprbpoxyvinylsilane, tributoxyvinylsilane, tripentoxyvinylsilane, tris ( ⁇ -methoxyethoxy) -vinylsilane, allylsilanesilanesilanesilanesiloxy, triethoxylanesilane, triethoxyallylsilane, triethoxyallylsilane, triethoxyallylsoxyane , withthacryloxyméthylméthoxysilane, acryloxyéthyltriméthoxysilane, usethacryloxyméthylméthoxysilane, acryloxyéthyltriméthoxysilane, acryloxyéthyltriméthoxysilane, orthacryloxyéthyltriméthoxysilane, acryloxyéthyltriméthoxysilane, methacryloxy
• CH 2 CH - Si - (OCH 2 CH 3 ) 3 vinyltriethoxysilane (VTEO)
• CH 2 CH - Si - (OCH 2 OCH 2 CH 3 ) 3 vinyltrimethoxyethoxysilane (VTMOEO) and (3- (methacryloxy) propyl) trimethoxysilane.
• CH 2 C (CH 3 ) - CO - 0 - (CH 2 ) 3 - Si (OCH 3 ) 3
• Polyolefins can be grafted in the molten state in the presence of radical initiator (s).
• the grafting reaction is carried out in a single or twin screw extruder fed with polyolefins in a feed hopper, for example in the form of granules; ue in the first zone of the extruder, one proceeds to the melting polyolefins by c: .. f wise and in a second zone, the reactants are introduced in the mass foncue polyolefins.
• the radical initiators can be chosen from peroxides, peracids, peresters, peracetals. They are generally used in an amount of 0.01% to 0.5% by mass relative to the polyolefins to be grafted.
• peroxides peracids
• peresters peracetals. They are generally used in an amount of 0.01% to 0.5% by mass relative to the polyolefins to be grafted.
• the reagent introduction zone is long enough and at a temperature low enough to ensure good dispersion of the reactants and the lowest possible thermal decomposition of the radical initiator.
• the actual grafting reaction takes place in a third zone of the extruder at a temperature capable of ensuring the total decomposition of the radical initiator; before the outlet of the melt at the head of the extruder, a degassing zone is provided where the decomposition products of the initiator and the unreacted vinylsilane are degassed, for example under vacuum.
• the grafted polyolefins are recovered at the extruder outlet, for example in the form of granulated rods after cooling in cold air.
• the weight ratio of the grafts to the grafted polymer is generally between 0.1 and 5% and preferably 0.15 to 2.5%.
• the polyolefins which are grafted with unsaturated epoxides can be chosen from the same group as those which are grafted with unsaturated alkoxysilanes.
• ethylene / alkyl (meth) acrylate copolymers are used.
• unsaturated epoxides there may be mentioned in particular glycidyl esters and ethers, glycidyl itaconate, vinyl glycidyl ether, allyl glycidyl ether, vinylcyclohexenemonoxide.
• unsaturated epoxides very particularly preferred is acrylate and glycidyl methacrylate.
• acrylate and glycidyl methacrylate are particularly preferred.
• the same process can be used as for grafting the unsaturated alkoxysilanes.
• the epoxide can be chosen from the same family as those already mentioned for the binders which are polyolefins grafted with unsaturated epoxides.
• This copolymer of ethylene and at least one unsaturated epoxide can also comprise an alkyl (meth) acrylate or vinyl acetate.
• the alkyl (meth) acrylate can be chosen from the same family as mentioned above for the possible comonomers of the polyolefins grafted with unsaturated alkoxysilanes.
• copolymers of ethylene and of at least one unsaturated epoxide mention may be made of copolymers of ethylene, of an alkyl (meth) acrylate and of glycidyl methacrylate containing by weight 2 to 10% preferably 6 to 8% glycidyl methacrylate and at least 50% ethylene.
• coil 1 and coil 2 the layer of silicon oxide deposited in plasma is 200 angstroms and PET 12 microns.
• b ethylene-butyl acrylate-maleic anhydride copolymer with 3% maleic anhydride with 15% acrylate with a melt index of 5 dg / min.
• ç ethylene-methyl acrylate copolymer identical to grafted at 0.45% by weight with vinyltrimethoxysilane.
• the peel strength of the silicon oxide coated PET binder complexes was measured.
• Ethylene / methyl acrylate binders of the same composition as the binder were prepared with different grafting rates of vinyltrimethoxysilane.
• the grafting rate is by weight of graft relative to the grafted polymer.
• the binder / PET film complex coated with silicon oxide was prepared by heat sealing.
• the thickness of the binder film is 350 ⁇ m.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Health & Medical Sciences (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Wood Science & Technology (AREA)
• Laminated Bodies (AREA)
• Compositions Of Macromolecular Compounds (AREA)
• Adhesives Or Adhesive Processes (AREA)
• Graft Or Block Polymers (AREA)

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• 1994
  • 1994-06-30 FR FR9408090A patent/FR2721939B1/fr not_active Expired - Fee Related
• 1995
  • 1995-06-28 US US08/604,962 patent/US5731092A/en not_active Expired - Fee Related
  • 1995-06-28 KR KR1019960701016A patent/KR100241582B1/ko not_active IP Right Cessation
  • 1995-06-28 EP EP05076517A patent/EP1609593A3/de not_active Withdrawn
  • 1995-06-28 EP EP95924377A patent/EP0716631A1/de not_active Ceased
  • 1995-06-28 WO PCT/FR1995/000860 patent/WO1996000656A1/fr not_active Application Discontinuation
  • 1995-06-28 AU AU28908/95A patent/AU691937B2/en not_active Ceased
  • 1995-06-28 CN CN95190598A patent/CN1079322C/zh not_active Expired - Fee Related
  • 1995-06-28 CA CA002169378A patent/CA2169378C/fr not_active Expired - Fee Related
  • 1995-06-28 JP JP8502877A patent/JP3065354B2/ja not_active Expired - Fee Related
• 1996
  • 1996-02-09 NO NO960535A patent/NO302742B1/no unknown
  • 1996-02-28 FI FI960928A patent/FI115899B/fi active IP Right Grant

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