WO2000015728A1 - Revetements en polyurethane pouvant etre reactives par la chaleur et leur utilisation en tant qu'adhesifs - Google Patents

Revetements en polyurethane pouvant etre reactives par la chaleur et leur utilisation en tant qu'adhesifs Download PDF

Info

Publication number
WO2000015728A1
WO2000015728A1 PCT/US1999/021118 US9921118W WO0015728A1 WO 2000015728 A1 WO2000015728 A1 WO 2000015728A1 US 9921118 W US9921118 W US 9921118W WO 0015728 A1 WO0015728 A1 WO 0015728A1
Authority
WO
WIPO (PCT)
Prior art keywords
coating
film
polyurethane
heat
sealing
Prior art date
Application number
PCT/US1999/021118
Other languages
English (en)
Inventor
Bruno R. L. Gringoire
Lajos E. Keller
Christian Leger
Original Assignee
Mobil Oil Corporation
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from GBGB9820121.3A external-priority patent/GB9820121D0/en
Application filed by Mobil Oil Corporation filed Critical Mobil Oil Corporation
Priority to AU59233/99A priority Critical patent/AU5923399A/en
Priority to JP2000570257A priority patent/JP2003525958A/ja
Priority to BR9913739-9A priority patent/BR9913739A/pt
Priority to EP99946931A priority patent/EP1127095A4/fr
Priority to CA002344340A priority patent/CA2344340A1/fr
Publication of WO2000015728A1 publication Critical patent/WO2000015728A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04—Coating
    • C08J7/052—Forming heat-sealable coatings
    • 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
    • B32B27/38—Layered products comprising a layer of synthetic resin comprising epoxy resins
    • 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 form; Layered products having particular features of form
    • B32B3/26—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar form; Layered products having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer
    • B32B3/266—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar form; Layered products having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer characterised by an apertured layer, the apertures going through the whole thickness of the layer, e.g. expanded metal, perforated layer, slit layer regular cells B32B3/12
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/0804—Manufacture of polymers containing ionic or ionogenic groups
    • C08G18/0819—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups
    • C08G18/0823—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups containing carboxylate salt groups or groups forming them
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6633—Compounds of group C08G18/42
    • C08G18/6637—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38
    • C08G18/6648—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3225 or C08G18/3271 and/or polyamines of C08G18/38
    • C08G18/6651—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3225 or C08G18/3271 and/or polyamines of C08G18/38 with compounds of group C08G18/3225 or polyamines of C08G18/38
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04—Coating
    • C08J7/0427—Coating with only one layer of a composition containing a polymer binder
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04—Coating
    • C08J7/043—Improving the adhesiveness of the coatings per se, e.g. forming primers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04—Coating
    • C08J7/046—Forming abrasion-resistant coatings; Forming surface-hardening coatings
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04—Coating
    • C08J7/056—Forming hydrophilic coatings
    • 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
    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/20—Adhesives in the form of films or foils characterised by their carriers
    • C09J7/22—Plastics; Metallised plastics
    • 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
    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/20—Adhesives in the form of films or foils characterised by their carriers
    • C09J7/22—Plastics; Metallised plastics
    • C09J7/24—Plastics; Metallised plastics based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C09J7/241—Polyolefin, e.g.rubber
    • C09J7/243—Ethylene or propylene polymers
    • 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
    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
    • C09J7/35—Heat-activated
    • 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
    • B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
    • B32B37/14—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers
    • B32B37/24—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with at least one layer not being coherent before laminating, e.g. made up from granular material sprinkled onto a substrate
    • B32B2037/243—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
    • B32B2309/00—Parameters for the laminating or treatment process; Apparatus details
    • B32B2309/02—Temperature
    • 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
    • B32B2309/00—Parameters for the laminating or treatment process; Apparatus details
    • B32B2309/04—Time
    • 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
    • B32B2363/00—Epoxy resins
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2170/00—Compositions for adhesives
    • C08G2170/20—Compositions for hot melt adhesives
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2475/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • 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
    • C09J2423/00—Presence of polyolefin
    • C09J2423/006—Presence of polyolefin in the substrate
    • 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
    • C09J2463/00—Presence of epoxy resin
    • C09J2463/003—Presence of epoxy resin in the primer coating
    • 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
    • C09J2475/00—Presence of polyurethane

Definitions

  • This invention relates to sheets coated with heat-activatable coatings, their production, and their uses in forming sealed packages and in lamination applications.
  • heat-activatable adhesive coatings on films and other sheets. These heat-activatable coatings can either be for heat sealing or cold sealing.
  • a heat-sealable, heat-activatable, coating is one which has to be heated to render it tacky and is pressed against the surface to which it is to adhere while it is still tacky. Often the heating and the pressing are conducted simultaneously using heated jaws.
  • a cold-sealable, heat-activatable, coating is one which is activated by heating generally until it is tacky, it is then allowed to cool during which time its tackiness may decrease, and is then pressed without significant heating against a receiving surface to which it adheres.
  • the jaws or other device for causing the pressing are usually at ambient temperature (e g., 25°C) but may be heated slightly, e.g., up to 30 or 35°C, or may be cooled (e. , to 0°C or below, for instance when packaging ice cream or other frozen or chilled products).
  • the receiving surface is another coating of the same material. Good sealing usually requires that the cold sealing is effected before the coating loses all its tacky feel
  • Heat-activatable adhesive coatings formed mainly of thermoplastic polyurethane are described in EP-A-574803 and, especially, in CA-A-2174288.
  • the normal way of applying the coating to the film or other sheet material is by coating a liquid coating composition containing the appropriate coating solids onto a sheet as the sheet travels continuously past a coating station, evaporating the liquid carrier, and thereby forming a tacky coating, cooling the tacky coating to render it non tacky, and then winding the coated sheet into a roll. It is important that the coating does not block or otherwise bond to the reverse face of the sheet in the roll since otherwise it is difficult, inefficient or impossible to unwind the roll. In practice therefore it is generally desirable that the coating should lose adhesive activity as fast and as fully as possible during the cooling step, so as to minimise the risk of blocking.
  • the coating When the coating is to be used for hot sealing, it is desirable that it should be capable of being heated easily and quickly to form a tacky coating, and that this should give a good seal when hot pressed to the receiving surface It is an unfortunate fact that coatings that give a good seal under these conditions tend to have tend to be rather slow at losing their sealing activity during the cooling step in initial manufacture, and may have some tendency to block in the roll. It is particularly difficult to obtain a good balance between blocking and sealing when the coating is to be used for cold sealing. Cold sealing is particularly important when the adhesive is to be applied to a packet containing heat sensitive material, such as chocolate or other low melting material, ice cream or other chilled or frozen material, or various other food stuffs.
  • heat sensitive material such as chocolate or other low melting material, ice cream or other chilled or frozen material, or various other food stuffs.
  • the heat from the heated jaws or other means for heat sealing might damage the material in the package. Accordingly it is desirable to activate the coating by heating at one station in the production line, insert the heat sensitive material in the package at a subsequent station, and then cold seal around the packaged material at a third station (while the coating is still activated). If the coating is to give a good cold seal, it must remain active for a significant period after the activation station. Unfortunately this means it will remain active for a significant period at the cooling stage during initial manufacture Accordingly coatings which give a good cold seal have a tendency to give major blocking problems when the film is initially coated and wound-up during initial manufacture. If blocking is low and satisfactory, an inadequate seal tends to be obtained when the time between the heating station and cold sealing station is sufficiently long to avoid damage to the heat sensitive ingredients.
  • the described coatings can include hydrophobic auxiliaries and various commercial auxiliaries and additives. It is said that the packaged film can be used for heat sealing or that it can be used by heat-activating the film and then simultaneously or within 10 minutes cooling below the melting point and cold sealing it. Although it is also asserted that the film surfaces can, after cooling, be brought into contact with one another without adhesion and low blocking values were recorded in a laboratory test, it also warns that rolling up the film with a release paper may be necessary to avoid blocking if the cooling is inadequate during manufacture.
  • Cold sealing properties and low blocking are relatively easy to achieve when the processing conditions and materials are relatively non-challenging, for instance when the coating equipment is very lengthy and/or when the film speed during initial manufacture is relatively slow (so that there is plenty of time for thorough deactivation before the film is wound up), or when the reverse face of the film is repellent to the coating.
  • the polyurethanes described in CA-A-2, 174,288 cannot satisfactorily be used on many substrates simultaneously to give low blocking during high speed commercial manufacture of a roll on the one hand and subsequent good heat sealing or cold sealing on the other. On many substrates, if good heat or cold sealing is achieved then blocking in the roll is a problem, but if blocking is not a problem then cold or hot sealing tends to be inferior
  • Blocking tendency may be low with, for instance uncoated polypropylene but may be high when the surface has polar properties, for instance of the type that are generally required to make that face printable by convenient printing inks.
  • blocking may be a particular problem when the reverse face is coated with a hydrophilic acrylic coating.
  • a coated sheet carrying a heat-activatable adhesive coating of coating solids which are mainly thermoplastic polyurethane, and have a melting point of 40 to 100°C.
  • the coating on the sheet is crystalline and has an average crystal size of below 10 ⁇ m
  • the actual crystal size is influenced to some extent by the thickness of the coating and the conditions by which the cooled crystalline coating is achieved.
  • the coating can be defined in terms of the time the coating, after being molten, remains tacky when cooled at 25°C.
  • a coated sheet wherein the coating remains tacky when pressed on itself, for at least 2 seconds but not more than 50 seconds when cooled at 25°C from the molten state.
  • a molten coating of the desired thickness on the desired substrate is formed at or just above the melting point of the compositions, and the time for the coating to become non-tacky when exposed to an ambient atmosphere at 25°C is measured.
  • the coating is usually molten in an oven at 100°C and is then exposed to an ambient temperature of 25°C. The methods for determining crystal size and tack are described in more detail below.
  • the preferred coating on the sheet is a coating which remains tacky for at least 5 seconds but not more than 50 seconds upon cooling at 25°C from the molten state. In general, this period of tackiness seems to be associated with the preferred crystal sizes, which are preferably in the range 0.5 to 5 ⁇ m.
  • the duration of tackiness is preferably at least 10 seconds and usually less than 40 seconds and preferably less than 30 seconds, e.g., 10 to 30 seconds or 10 to 20 seconds.
  • the period during which the coating can be cold sealed is usually somewhat less than the period of tackiness, but the period of tackiness is a useful guide to the sealing and blocking properties of the coating and for convenience is referred to herein as the deactivation period
  • the invention makes it possible to obtain a better compromise between sealing performance and blocking problems.
  • it is now possible to reduce the tendency for blocking problems to increase in proportion to sealing performance In particular we can achieve reduced blocking problems against most of the typical polar surfaces at any particular cold (and/or hot) sealing performance.
  • it is now possible to obtain improved cold seal (and/or hot seal) performance The invention allows the conduct of fast commercial coating and sealing processes (for instance by selection of coating thickness, coating temperature, activation temperature and film speeds) that give an improved combination of good cold (and/or hot) sealing performance benefits with reduced blocking problems.
  • the composition of the adhesive coating so as to achieve much smaller crystal size, and in practice this is associated with faster crystallisation and shorter duration of deactivation.
  • this is associated with faster crystallisation and shorter duration of deactivation.
  • the preferred coatings have a crystal size of not more than 2 ⁇ m. Crystal sizes as low as this are associated with a significantly reduced blocking tendency with the result that the film or other sheet material can be coated on a high speed compact production line with minimum risk of blocking.
  • the crystal size is at least 0.3 or 0.5 ⁇ m. Best results for cold sealing applications seem to be achieved with a crystal size in the range 0.7 to 3, preferably 0.7 to 2 ⁇ m. However the very low crystal sizes, for instance down to 0 1 or 0.3 ⁇ m, can be used for heat sealing applications, depending on the choice of wax or other way of controlling crystal size.
  • thermoplastic polyurethane preferably has hydrophilic groups which render it water- dispersible.
  • the polyurethane, and the total composition of coating solids and the coating itself each have a melting point of from 40 to 100°C, generally 40 to 70° or 80°C. Best results are achieved with a melting point of around 50 to 70°C If the melting point is too low, there is increased tendency towards blocking
  • the polyurethane, and the coating solids of the coating preferably has an enthalpy of fusion in the defined melting range of at least 20 J/G and often at least 50 J/G, for instance 60 to 100 J/G.
  • the polyurethane must be one which crystallises on solidifying from the molten or tacky state.
  • it is formed from reaction of polyfunctional isocyanate and a mixture of high molecular weight (usually M w 500 to 5000 or higher) polyol and low molecular weight (usually M w 60 to 500) polyol, the polyols often being diols
  • the high molecular weight diol or other polyol preferably has a melting point of from 30 to 100°C and an enthalpy of fusion in this temperature range of at least 50 J/G.
  • Additional monomers that may be incorporated for forming the polyurethane are other hydroxy or amino compounds and other monomers which will introduce potentially hydrophilic groups so as to render the polyurethane water dispersible
  • the molecular weight of the polyurethane may be selected to any chosen value (typically in the range 10,000 to 100,000) by selecting monomers and their amounts, and the polymerisation conditions, in conventional manner
  • the coating solids i.e., the total materials in the actual coating
  • at least 60%, and normally at least 80% and generally at least 90% by weight of the coating solids are such a polyurethane
  • additives include thickeners, thixotropes, colourants, dyes and pigments together with fillers and blowing agents or any other conventional additives.
  • the additives are preferably such that the coating remains optically clear.
  • Preferred emulsifiers are aryl sulphonates.
  • the preferred amounts are 0.05 to 10% by weight based on solids, generally 0.1 to 3%
  • antifoam is present Suitable antifoams are silicone antifoams, typically added in amounts of 1 to 50, typically 2 to 10, parts per million, based on the aqueous dispersion.
  • a slip aid is included in the coating composition so as to reduce the coefficient of friction coating/metal plate (COF) and to improve slip behaviour on the coating machines and on the packaging machines.
  • slip additives can be any of the conventional mineral or synthetic particles known for this purpose, generally having a size of 0.1 to 10 ⁇ m. Suitable materials include silicones, polymethyl methacrylates and various other minerals.
  • the total amount of slip aid is generally in the range 0.1 to 5% by weight of coating solids, most preferably 0.3 to 1%) by weight of coating solids
  • the coating has COF below 0.25, preferably 0.1 to 0.2, and if the coating without slip aid has a higher COF it is preferred to include sufficient of slip aid to reduce the COF to the desired value
  • the total amount of these minor additives is usually below 20% and preferably below
  • the coating solids are formulated so as to provide a coating having the desired crystallisability and/or deactivation period.
  • One way of achieving this is by appropriate selection of the polyurethane component. Conventional reproduction of the manufacturing processes described in CA-A-2, 174,288 will tend to give a polyurethane having an essentially monomodal molecular weight distribution.
  • At least 10% and generally at least 30% by weight of the polyurethane can be a relatively low molecular weight polyurethane, for instance having a substantially monomodal distribution of from 10,000 to 45,000, often around 20,000 to 30,000, and at least 10% and generally at least 30% by weight of the polyurethane has a higher molecular weight distribution, for instance being a monomodal molecular weight distribution with an average of from 50,000 to 100,000, often around 50,000 to 70,000
  • the proportions of low and high molecular weight polyurethanes are 2: 1 to 1 :2, generally around 1 : 1 by weight. If desired, three or more polyurethanes may be blended.
  • polyurethane has an essentially monomodal distribution with an average molecular weight of at least 10,000 and usually at least 20,000 and most usually at least 30,000, but usually not more than 80,000 or, at most, 100,000 We find best results are generally obtained in the range 30,000 to 60,000.
  • the monomodal molecular weight distributions used in the invention generally reflect a M w /TVI n ratio of between 15 and 1, generally between 5 and 1. With a monomodal distribution the preferred crystal size and/or deactivation period generally is not obtained unless a crystallisation initiator is included in the coating solids.
  • the preferred coating solids in the invention include a crystallisation initiator whereby the size of the crystals is reduced relative to the same coating solids underthe same test conditions but formed in the absence of the crystallisation initiator
  • a crystallisation initiator it may be referred to as a nucleating agent
  • Crystallisation depends upon the interaction between the polymer and the additive or additives in the coating solids which promote crystallisation
  • the polymer it should be one which has a molecular structure which permits crystalline ordering and which can crystallise at a temperature below the melting point but preferably not too close to the glass point.
  • this additive should be a material which has a melting point higher than the melting point of the polymer, which is insoluble in the polymer but which is wetted or absorbed by the polymer and which can be homogeneously dispersed in a melt of the coating solids as a very fine dispersion.
  • the overall effect of the additive should be to increase the isothermal recrystallisation velocity of the composition from a molten state and which will promote a spherulitic crystalline superstructure and reduce the crystal size to the desired size, as a consequence of this.
  • Nucleating agents for crystallisable melts are well known and materials suitable for any particular coating composition or coating can be found by routine testing. Mixtures of materials may be used to provide the nucleation or crystallisation effect which is required in the invention. Indeed, some suitable additives are themselves mixtures of materials, for instance various waxes.
  • Preferred waxes are hydrocarbon waxes which melt at a higher temperature than the polyurethane, and which preferably melt at above 80°C and generally above 100°C, for instance at 100 to 150°C.
  • paraffin waxes having a melting point of, for instance, above 50°C can be suitable with some polymers, it is generally preferred to use higher melting waxes such as waxes having melting points of 50 to 150°C, preferably 80 to 130°C
  • the waxes can be cyclic or branched hydrocarbon waxes but are preferably substantially linear, aliphatic, saturated waxes. Fischer Tropsch waxes are particularly suitable.
  • Waxes which are based on aliphatic and/or aromatic esters or mixtures of these optionally with fatty acids and/or fatty alcohols, ketones or hydrocarbons can also be used.
  • Suitable ester waxes are Carnauba and, especially, Montan wax.
  • waxes since they can migrate to the surface and provide further reduction in blocking (in addition to the reduction in crystal size and/or deactivation period), and in COF, by a surface effect
  • nucleating agents can be selected from (depending upon the particular polymer) conventional inorganic nucleating agents such as kaolin, silica and talc and conventional organic nucleating agents such as salts of acids (for instance lithium benzoate) aryl sulphonates and certain pigments, as well as waxes and particular polymers such as ethylene/acrylic acid copolymers
  • inorganic nucleating agents such as kaolin, silica and talc
  • organic nucleating agents such as salts of acids (for instance lithium benzoate) aryl sulphonates and certain pigments, as well as waxes and particular polymers such as ethylene/acrylic acid copolymers
  • the amount of the crystallisation initiator will be selected so as to promote the desired crystal size. It is usually at least 0 1% by weight of the solids and generally at least 0.5%) It is usually below 20% and usually below 7% by weight of the coating solids. Best results are generally obtained with from 0.5 to 5, generally 0 5 to 2.5, parts crystallisation initiator per 100 parts coating solids Since the coating solids are mainly polyurethane, the amount can alternatively be expressed as 0 5 to 5, preferably 0 5 to 2 5, parts by weight initiator per hundred parts polyurethane.
  • the coating composition should be formulated so that it does not interfere with the optical properties of the coating or the coated film.
  • the coating should be substantially clear and transparent, and so the selection of the initiator and the other components of the coating is preferably made so as to minimise any tendency towards opacity or translucency in the coating when it has crystallised
  • the reduction in crystal size achieved in the invention is beneficial in this respect since the transparency of the coating will generally tend to improve as the crystal size is reduced, with the coatings having very small crystal size being substantially wholly transparent. This is of particular benefit when the sheet substrate which is coated is itself transparent.
  • the coated sheets of the invention are made by applying a coating composition containing the coating solids to the sheet
  • the method of production is preferably continuous and thus the preferred processes of the invention comprise continuously forming a coating by applying the coating solids to the film and then winding up the coated film or other sheet.
  • the coating initially has to be in a liquid form in order that in can be applied and thus the coating initially goes through a tacky state.
  • the process generally involves cooling the coating to render it non-tacky, and the coated film should therefore not be wound up until it is non-tacky and until the tendency to blocking is sufficiently low.
  • the liquid form of the composition during its application to the sheet can be a melt, solution, emulsion or dispersion
  • the coating could be applied by a melt coating technique through a dye or other melt coater
  • the composition is an aqueous composition, preferably an emulsion or dispersion of the coating solids in water. It may be applied by any convenient technique, preferably by a gravure roll such as in direct gravure technology.
  • the coating solids preferably include emulsifier and antifoam, as discussed above, in order to facilitate the application of the coating.
  • the total solids content of the aqueous dispersion or emulsion is generally in the range 10 to 60%, preferably 20 to 40%, by weight
  • the coating is generally applied to the film or other sheet material by any conventional doctor blade, roller coating or other coating mechanism.
  • the dry weight of the coating is usually at least 0.3, and preferably at least 0.5 g/m 2 . There is usually no need for it to be more than 5 g/m 2 and usually it does not have to be more than 3 g/m 2
  • a particular advantage of the invention is that good results are obtained at low coating weights of below 2g/m 2 , for instance 0.5 to 1.9 g/m 2 .
  • Suitable coating thicknesses are from 0 5 to 2 ⁇ m
  • the coating is fluid when it contacts the film and it is usually necessary to heat the coating in order to drive off the water or other liquid carrier
  • the film is usually either coated in an oven or passes through an oven substantially immediately after coating, the oven being at a suitable temperature to drive off the water or other liquid carrier.
  • the oven is at a temperature of 50 to 100°C or more, usually at a temperature of above 90°C.
  • the heating temperature is usually above the melting point of the coating solids and the coating.
  • the coating procedure results in the formation of a tacky coating. In the invention, the coating is then cooled so as to render it non-tacky.
  • the cooling can be by mere exposure to ambient conditions but preferably the coated film is chilled by a chill roll and/or by a forced air stream at the desired cooling temperature so as to accelerate the cooling
  • air at, for instance, 5 to 30°C, often 25°C can be blown across the tacky coating
  • Accelerating the cooling and/or providing a low coating weight can both contribute to the formation of the desired small crystal size, irrespective of the choice of nucleating agent or other combination of materials to promote crystallisation.
  • the cooling must not only render the surface non-tacky to the touch, but must also result in the coating having a suitably low tendency to blocking when it is wound up at the end of the coating operation.
  • the duration between the start of cooling and the winding is from 1 to 20 seconds, most preferably 3 to 10 seconds.
  • the sheet is generally travelling past the coating station and to the winder at a speed of from 200 to 1000 metres per minute, preferably 250 to 600 metres per minute.
  • the coating can be a continuous coating, i e , an overall coating, or it can be discontinuous. For instance the coating can be applied only to patches, strips or other regions where adhesion will be required.
  • the coating weights mentioned above relate to the weight per square metre that is actually coated.
  • the sheet material can be any sheet which is to be bonded by hot or cold sealing to another surface.
  • the sheet can be, for instance, a paper sheet cardboard or metal foil but preferably the sheet material is a polymeric film
  • the preferred film is a polyolefin film such as a film based on polyethylene, polypropylene, polybutylene, or a copolymer or terpolymer of ethylene and or propylene and/or butylene, with polyethylene or polypropylene being the preferred film.
  • This film may be constituted by several layers of different polymers which are coextrdued, the main layer in weight, being polypropylene or polyethylene.
  • At least one external side of the film could be constituted by polyethylene, polypropylene, copolymer PE-PP, terpolymer PE-PP-polybutylene, copolymer ethylene-vinyl alcohol, or any other type of extrduable polymer.
  • Other polymeric films include PET or other polyester films, polyamide films, polyacrylonitrile films, cellulose derivative films, polyacrylate films, polystyrene and other polyaromatic films and polyvinyl films such as films based on polyvinyl chloride, polyvinylidene chloride and polyvinyl acetate. Films based on copolymers may be used.
  • the films may have been made by conventional film-forming techniques to a thickness of, typically, 3 ⁇ m to 5,000 ⁇ m, preferably 10 ⁇ m to 200 ⁇ m
  • the films may be made extrusion, coextrusion, coating or lamination.
  • the films can consist of a single layer or a laminate. They may be unoriented or they may be monoaxially or biaxially oriented. They may be cavitated (for instance as a result of biaxial orientation of a film containing a cavity-formation component such as spheres of polybutyl terephthalate as described in US patents No 4,632,869 and 4,720,416, or any other type of particles including some cavities)
  • the films may contain conventional additives such as dyes, pigments, antistatic additives and stabilisers.
  • the surface of the film on to which the polyurethane coating is to be applied may carry a suitable primer in order to improve adhesion, for instance if the film would otherwise give poor adhesion.
  • Suitable primers depend upon the composition of the coating solids and the nature of the film and are selected in conventional manner from conventional primers such as polyimines, polyurethanes, polyesters, polyethers, polyacrylates, chlorinated polypropylene and epoxy primers.
  • the adhesion of the primer to the film, or the adhesion of the polyurethane coating to the film can be improved by for instance corona, flame or plasma treatment of the film surface if desired. It is naturally necessary to select the polyurethane, the film substrate, and the primer (if present) in conventional manner so as to obtain appropriate coating and bonding.
  • the polypropylene film may comprise a polypropylene core with one or more coextruded facing layers.
  • the core may be a microvoided core
  • the reverse face of the film can be non-polar but the invention is of particular value when the reverse face of the film is polar (for instance so that the film is printable). There would (prior to the invention) then be a particular tendency for the polyurethane to block against the polar reverse face of the film when the coated film is wound up
  • the polar properties can be provided by a primer or by flame, corona, plasma, electron beam or chemical grafting.
  • a hydrophilic acrylic coating on the reverse face of the film for instance an acrylic coating.
  • Another useful embodiment of the invention arises when the reverse face of the film is coated with a material to which significant blocking does not occur in the roll but to which heat sealing can be effected by the application of appropriate heat and pressure at a subsequent stage.
  • the reverse face can be coated with an acrylic coating composition or with a polyvinylidene chloride coating composition.
  • the coated film may have the crystallisable polyurethane coating on one face and the other face may be metallised with aluminium or otherwise treated with silane, oxide or other metal.
  • the invention also includes processes where the crystalline polyurethane is applied over a preliminary coating of metal, oxide or silane or other barrier-improving substrate for the polyurethane.
  • the film or other sheet carrying the adhesive polyurethane coating is laminated to a receiving sheet by the adhesive coating, either by hot sealing or by cold sealing.
  • the sheet material which is to serve as the receiving sheet may be formed from any of the films or sheet materials discussed above as the substrate for the adhesive polyurethane coating.
  • the surface of the receiving sheet material to which the adhesive coating is to be bonded is itself a coating on a substrate, for instance a coating of polyvinylidene chloride, acrylic polymer, polyvinyl alcohol, epoxy, or polyurethane
  • the coated sheet material is to be bonded to another piece of the same material or it may be bonded to itself to form a package
  • the coated sheet may be folded upon itself and then end sealed and/or edge sealed either with the polyurethane-coated face bonded to the reverse face of the film to form a flat seal or two polyurethane-coated surfaces may be bonded in face-to- face contact to each other as a fin seal, both polyurethane coatings preferably being in accordance with the invention.
  • the bonding may be achieved by activation of the coating followed by sealing, or by simultaneous activation and sealing. Usually it is preferred to preactivate the coating.
  • the preactivation can be by conduction, convection or radiation.
  • it can be by infra-red radiation, hot air or through contact with a heated surface
  • Activation by methods that do not require contact between a heated surface and the film is generally preferred, for instance hot air or, preferably, infra-red radiation
  • the coating on the film, during the activation is generally heated to close to or above its melting temperature.
  • the activation must be sufficiently intense to render the coating tacky and usually the maximum surface temperature of the coating during activation is from 50 to 160°C, preferably 80 to 130°C.
  • the entire coating may be activated if required, but it is often preferred to activate only those parts of the coating which are to be sealed, for instance in a pattern.
  • preferred films according to the invention have an overall heat-activatable coating but are then activated only in those regions where sealing is to occur For instance localised activation in this manner can be achieved by localised direct or indirect heating of the coating in the desired pattern of activation.
  • Sealing is applied after activation by pressing together by jaws the surfaces which are to be bonded to one another.
  • the duration between activation and the sealing step is normally such that the coating still feels tacky at the time it is sealed and so is usually less than the measured activation period for the coating. Generally therefore the period is from 3 to 30 or 40 seconds.
  • the jaws or other sealing apparatus can be located relatively close to the activation stage, even when cold sealing is to be used, and thus the packaging machinery can be very compact
  • the distance between the activation stage and the sealing stage is typically in the range 1 to 5 metres and the packaging speed is typically in the range 9 to 120 metres per minute.
  • the preactivation is generally applied prior to the forming collar of the packaging machine, and the sealing is applied subsequently by appropriate jaws
  • activated coating is cold sealed to the receiving surface while it is still activated.
  • the temperature of the sealing jaws is generally at about or below ambient (for instance 0 to 30°C) but if desired the jaws may be heated slightly for instance up to 35°C or 40°C, or other cool temperature well below the melting point of the coating.
  • the activated coating is hot sealed by the application of heated jaws, for instance having a temperature of less than 100°C, generally 40 to 80°C.
  • the invention is applied to the packaging of heat- sensitive components such as chocolate, ice cream or other foodstuffs, the coating is activated (usually before the forming collar) and then, at a position sufficiently distant from the activation heaters, the heat-sensitive component is wrapped in the activated sheet material to form a packet, and the sides and/or ends of the packet are then cold-sealed between cold jaws or other cold sealing apparatus.
  • the activation is confined solely to those areas where cold sealing is to be applied
  • cold sealing including cool sealing
  • the invention is used for cold sealing in which event a preferred process comprises heat activating the heat-activatable coating on the sheet or sheets and subsequently cold-sealing or cool-sealing the coating while still activated.
  • the invention can also be applied to substantially simultaneous activation and sealing processes in which the film is activated either by the sealing jaws or immediately ahead of the sealing jaws, i.e., with the activation heat and the sealing pressure being applied substantially simultaneously.
  • the bonding may be by heat sealing, in which event the sheets which are to be bonded to one another may be pressed together between heated jaws, i.e., appropriate other heated pressure applicators in conventional manner so as to provide melt sealing.
  • the jaws may be heated to above the meeting point of the coating, but an advantage of the invebtion is that cool sealing at for instance above 40°C, and often above 50°C up to 70°C or 80°C can give good results.
  • Suitable sealing machines are Horizontal Form Fill Seal (HFFS), Vertical FFS (VFFS), or other suitable machines.
  • the invention can also be applied for lamination of two sheet materials, for instance a film or other sheet coated with the crystallisable polyurethane of the invention and a receiving sheet which may be, for instance, board, film or other sheet which may be coated with crystallisable polyurethane or may be coated with other coating which will promote sealing (generally heat sealing) or may be uncoated.
  • the lamination may involve bonding over the entire interface between the two sheets (in which event a continuous coating of the polyurethane would be required) or it may merely involve localised bonding, for instance in stripes or other pattern.
  • the bonding used for lamination can involve cold sealing but it is usually convenient to conduct it by hot sealing either between two hot-heated rolls or between one cold roll and one hot roll, the latter generally being the roll which drives the polyurethane-coated film.
  • hot- sealing by this or other means is to be conducted the temperature of the heated roll or rolls should be above 50°C and preferably above 80°C
  • the crystal size is determined in the invention by examining the relevant film using an optical microscope to observe crystal sizes where most of the crystals are above 2 or 3 ⁇ m, and using an Atomic Force Microscope to determine smaller crystal sizes.
  • the operator selects a random area (or several random areas if there is significant variation between them) and measures the horizontal and vertical dimensions for a number of the crystals or spherulites that are observed, and thereby calculates the diameter of each spherulite.
  • a typical selection of a plurality of these spherulites is made and the average diameter is calculated from each of these.
  • a coated sheet is cut inwards from one edge into a series of parallel bands each 30 mm wide After the sheet is heated for one minute at 100°C in an oven in order to render the coating molten and tacky, the sheet is removed from the oven and exposed to ambient temperature. At 5 seconds, the first of the bands is pressed on itself and immediately peeled apart by hand. This is repeated at 10 seconds for the second band, 15 seconds for the third band and so forth. The last coating which shows significant tackiness when peeling the band away from itself indicates the time for which the coating remains tacky. Thus if the band at 30 seconds does feel tacky but the band at 35 seconds does not, the coating is assessed as remaining tacky for 30 seconds and as having a deactivation period of 30 seconds.
  • a polyurethane as described in CA-A-2, 174,288 is emulsified in water to give an emulsion having a 20% solids content together with 0.1% aryl sulphonate as emulsifier, 10 ppm of a silicone antifoam, and 0.5 parts (per hundred parts polyurethane) of a slip aid which is sold under the trade name Tospearl and which consists mainly of spherical cross linked particles having an average diameter 4.5 ⁇ m.
  • the coating composition is made by blending these ingredients using a pneumatic stirrer.
  • slip aid had the result that the coefficient of friction (COF) of films made from the coating, as discussed in the following examples, generally fell within the range 0.13 to 0.25, whereas in the absence of sufficient (or any) slip aid the typical COF for the composition is around 0 4 or higher
  • aqueous dispersion of example 1 was coated by a direct gravure process and the coated film was heated to 110°C so as to dry it and convert the polyurethane coating into an adhesive coating and was then cooled by air.
  • the crystal size in the resultant coating was determined by Atomic Force microscope or (for the larger crystal sizes) by optical microscope, as explained above.
  • the activation period (the time taken for the coating to be cooled down during manufacture from its temperature in the coating oven to the time when it no longer exhibited tacl , as explained above).
  • the polyurethane coated surface of the film was pressed against the reverse surface of the film 52.5 kg/cm 2 pressure was applied for 24 hours at 4°C in order to simulate what can happen in a roll
  • the films were then peeled apart and the peeling force was recorded as grams per 25 mm.
  • the blocking value is for the A/B configuration.
  • Cold sealing was conducted using a horizontal form fill seal (HFFS) packaging machine operating at various web speeds, usually 50 metres per minute or 80 metres per minute.
  • HFFS horizontal form fill seal
  • the jaws were at a temperature of 20°C and were located at a travel time of 1.8 seconds when the film is travelling at 50 m/min and 1.1 seconds when the film is travelling at 80 m/min, i.e., a linear distance of 1.5 metres from the activation stage which used short wave infra-red and generated a surface temperature of 60°C
  • the polyurethane coating was being pressed against, and sealed to, itself and thus the HFFS cold value is for the A/A configuration.
  • the film was not pre-activated but instead was subjected to heat sealing using heated jaws.
  • the heat seal was determined as an HFFS value at a draw temperature of 80°C and a film speed of 40 m/min for the A/A configuration.
  • the minimum sealing temperature which was required to reach a sealing strength of 250 g/25 mm for the A/A configuration was recorded The results are set out in the following tables.
  • Table 1 The results in Table 1 are the results obtained when the starting film is a 33 ⁇ m white cavitated polypropylene film having a density of 0 6 having coextruded surface layers of terpolymer of propylene, ethylene and butylene (Terpo) and which is reverse coated with an acrylic coating and coated on the other face with an epoxy primer. The polyurethane coating is then applied on to this primer.
  • F/T wax is Fisher Tropsch wax. TABLE 1
  • Test 5 shows that an improved combination of blocking and sealing can also be obtained by adding 2.5 phr (parts per hundred resin) paraffin wax.
  • the addition of montan wax gives a further improvement in blocking but with a slightly adverse effect on sealing properties and so if montan wax is used the amount may need to be optimised depending upon whether the primary objective is improved sealing or reduced blocking
  • carnauba wax was found to prevent cold sealing although it gave reasonable hot seal and good blocking properties. This cold sealing failure may have been due to unknown additive or other component in that particular sample of in the carnauba wax.
  • Test 6 shows that the best combination of blocking and sealing properties, combined with the smallest crystal size and a short activation period, is obtained using 2.5 parts Fischer Tropsch wax per hundred parts resin, as nucleating agent.
  • Table 2 show the effect of varying the nature of the base film (the film itself, its surface coating, its primer coating or its reverse surface) when applying a system otherwise similar to test 6, i.e., using polyurethane molecular weight 50,000 with 2.5 phr Fischer Tropsch wax.
  • film A is the 33 micron polypropylene cavitated white film having density 0.6.
  • Film B is a 35 ⁇ m polypropylene white cavitated film having a density of 0.72.
  • Film C is a 23 micron transparent plain polypropylene film having a density of 0.9
  • Film PET is a 12 ⁇ m plain transparent polyester film.
  • Film OPA is a 12 ⁇ m plain transparent polyamide film and the paper is an 80 ⁇ m sheet. In each instance the primer is applied over a surface coating and in each instance the reverse surface of the film had an acrylic coating or other specified treatment, except as shown.
  • Comparison of tests 6, 9 and 10 shows that, as with any film coating process, selection of the primer can have negative influence on the final properties of the film and that it is therefore necessary to optimise the primer with respect to the substrate and the heat-activatable composition, in accordance with conventional techniques.
  • Comparison of tests 6 and 11 show that even varying the density of the substrate film can influence results.
  • Tests 12 to 22 show that useful combinations of sealing and blocking can be obtained with a wide variety of substrates, including variations in the reverse face treatments of the substrates.

Abstract

Une feuille est revêtue d'une couche adhésive de polyuréthane thermoplastique pouvant être réactivé par la chaleur et dont le point de fusion est compris entre 40 et 100 °C. Le revêtement peut être cristallin et comporter des cristaux dont la taille moyenne est inférieure à 10 νm. En outre, ce revêtement, lorsqu'il est fondu, peut rester collant pendant une période comprise entre 2 à 50 secondes. Des procédés préférés consistent à réactiver ce revêtement par la chaleur, puis à le souder par pression à froid ou à température ambiante, par exemple pour empaqueter une matière thermosensible.
PCT/US1999/021118 1998-09-15 1999-09-14 Revetements en polyurethane pouvant etre reactives par la chaleur et leur utilisation en tant qu'adhesifs WO2000015728A1 (fr)

Priority Applications (5)

Application Number Priority Date Filing Date Title
AU59233/99A AU5923399A (en) 1998-09-15 1999-09-14 Heat-activatable polyurethane coatings and their use as adhesives
JP2000570257A JP2003525958A (ja) 1998-09-15 1999-09-14 熱活性化可能なポリウレタン被覆物及びその接着剤としての使用
BR9913739-9A BR9913739A (pt) 1998-09-15 1999-09-14 Revestimentos de poliuretana ativados pelo calor e seu uso como adesivos
EP99946931A EP1127095A4 (fr) 1998-09-15 1999-09-14 Revetements en polyurethane pouvant etre reactives par la chaleur et leur utilisation en tant qu'adhesifs
CA002344340A CA2344340A1 (fr) 1998-09-15 1999-09-14 Revetements en polyurethane pouvant etre reactives par la chaleur et leur utilisation en tant qu'adhesifs

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GBGB9820121.3A GB9820121D0 (en) 1998-09-15 1998-09-15 Heat-activatable polyurethane coatings and their use as adhesives
GB9820121.3 1998-09-15
US21579998A 1998-12-18 1998-12-18
US09/215,799 1998-12-18

Publications (1)

Publication Number Publication Date
WO2000015728A1 true WO2000015728A1 (fr) 2000-03-23

Family

ID=26314374

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1999/021118 WO2000015728A1 (fr) 1998-09-15 1999-09-14 Revetements en polyurethane pouvant etre reactives par la chaleur et leur utilisation en tant qu'adhesifs

Country Status (7)

Country Link
EP (1) EP1127095A4 (fr)
JP (1) JP2003525958A (fr)
AR (1) AR022093A1 (fr)
AU (1) AU5923399A (fr)
BR (1) BR9913739A (fr)
CA (1) CA2344340A1 (fr)
WO (1) WO2000015728A1 (fr)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007006583A1 (fr) * 2005-07-14 2007-01-18 Dsm Ip Assets B.V. Composition de polyurethanne supportee par un solvant
WO2007128789A1 (fr) * 2006-05-09 2007-11-15 Basf Se Feuille polyuréthane thermo-activable
DE202009015262U1 (de) 2009-07-30 2010-03-11 Lohmann Gmbh & Co. Kg Latent reaktive, hitzeaktivierbare Klebmasse und damit hergestellte Klebemittel
WO2011160912A1 (fr) * 2010-06-23 2011-12-29 Henkel Ag & Co. Kgaa Adhésif à contrecoller à base de tpu
US20150068060A1 (en) * 2011-12-27 2015-03-12 Hee-Dae Park Composite of adhesive films and shoe sole using same
EP2944662A1 (fr) 2014-05-16 2015-11-18 Henkel AG & Co. KGaA Adhésif thermofusible de polyuréthane thermoplastique
CN105694792A (zh) * 2014-12-15 2016-06-22 H.B.富乐公司 对金属表面具有改进的粘合性的反应性膜粘合剂
WO2018085039A1 (fr) * 2016-11-04 2018-05-11 Daybreak Technologies, Inc. Bandes et feuilles imprimées numériques ayant des couches d'amorces de polymère semi-interpénétrant
WO2018184082A1 (fr) * 2017-04-05 2018-10-11 Do Carmo Rafael Ricardo Matière collante pour le revêtement décoratif d'espaces ambiants
US11629273B2 (en) 2017-02-28 2023-04-18 3M Innovative Properties Company Polyurethane adhesive with chemical resistant
US11639316B2 (en) 2018-09-26 2023-05-02 3M Innovative Properties Company Fiber tows with a heat-activated sizing
WO2023152355A1 (fr) * 2022-02-14 2023-08-17 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung eingetragener Verein Film composite pour l'équipement permanent de moules avec une couche de séparation

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4581389B2 (ja) * 2003-12-12 2010-11-17 東亞合成株式会社 オレフィン系樹脂の接着方法
JP4581390B2 (ja) * 2003-12-12 2010-11-17 東亞合成株式会社 オレフィン系樹脂の接着方法
JP5281225B2 (ja) * 2003-12-12 2013-09-04 東亞合成株式会社 オレフィン系樹脂の接着方法
JP2006015675A (ja) * 2004-07-05 2006-01-19 Toray Ind Inc 建築材料用積層ポリエステルフィルム
BR112013010658B1 (pt) * 2010-11-01 2021-04-27 Dow Brasil S.A. Artigo, kit e método para modificar a superfície de um substrato de poliolefina
BR112018002508B1 (pt) * 2015-08-06 2022-11-16 Actega North America, Inc Composição de revestimento em dispersão aquosa formadora de película com aplicação como revestimento por selagem térmica para aplicações em embalagens do tipo blister

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5115073A (en) * 1989-09-23 1992-05-19 Bayer Aktiengesellschaft Rapidly crystallizing polyurethane systems
US5472785A (en) * 1994-04-12 1995-12-05 Minnesota Mining And Manufacturing Company Reactive wax-containing moisture curable hot melt composition
CA2174288A1 (fr) * 1995-04-20 1996-10-21 Ulrike Licht Films d'emballage revetus de polyurethane

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4419449A1 (de) * 1994-06-03 1995-12-07 Henkel Kgaa Schnell abbindender Polyurethan-Schmelzklebstoff

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5115073A (en) * 1989-09-23 1992-05-19 Bayer Aktiengesellschaft Rapidly crystallizing polyurethane systems
US5472785A (en) * 1994-04-12 1995-12-05 Minnesota Mining And Manufacturing Company Reactive wax-containing moisture curable hot melt composition
CA2174288A1 (fr) * 1995-04-20 1996-10-21 Ulrike Licht Films d'emballage revetus de polyurethane

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP1127095A4 *

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8492458B2 (en) 2005-07-14 2013-07-23 Dsm Ip Assets B.V. Solvent borne polyurethane composition
WO2007006583A1 (fr) * 2005-07-14 2007-01-18 Dsm Ip Assets B.V. Composition de polyurethanne supportee par un solvant
WO2007128789A1 (fr) * 2006-05-09 2007-11-15 Basf Se Feuille polyuréthane thermo-activable
DE202009015262U1 (de) 2009-07-30 2010-03-11 Lohmann Gmbh & Co. Kg Latent reaktive, hitzeaktivierbare Klebmasse und damit hergestellte Klebemittel
DE102010013145A1 (de) 2009-07-30 2011-02-03 Lohmann Gmbh & Co. Kg Latent reaktive, hitzeaktivierbare Klebmasse und damit hergestellte Klebemittel
CN102947365B (zh) * 2010-06-23 2016-03-16 汉高股份有限及两合公司 Tpu层压粘合剂
WO2011160912A1 (fr) * 2010-06-23 2011-12-29 Henkel Ag & Co. Kgaa Adhésif à contrecoller à base de tpu
CN102947365A (zh) * 2010-06-23 2013-02-27 汉高股份有限及两合公司 Tpu层压粘合剂
US9605191B2 (en) * 2011-12-27 2017-03-28 Hee-Dae Park Composite of adhesive films and shoe sole using same
US20150068060A1 (en) * 2011-12-27 2015-03-12 Hee-Dae Park Composite of adhesive films and shoe sole using same
EP2944662A1 (fr) 2014-05-16 2015-11-18 Henkel AG & Co. KGaA Adhésif thermofusible de polyuréthane thermoplastique
CN105694792A (zh) * 2014-12-15 2016-06-22 H.B.富乐公司 对金属表面具有改进的粘合性的反应性膜粘合剂
CN105694793A (zh) * 2014-12-15 2016-06-22 H.B.富乐公司 对金属表面具有改进的粘合性的反应性粘合剂
WO2018085039A1 (fr) * 2016-11-04 2018-05-11 Daybreak Technologies, Inc. Bandes et feuilles imprimées numériques ayant des couches d'amorces de polymère semi-interpénétrant
US11629273B2 (en) 2017-02-28 2023-04-18 3M Innovative Properties Company Polyurethane adhesive with chemical resistant
WO2018184082A1 (fr) * 2017-04-05 2018-10-11 Do Carmo Rafael Ricardo Matière collante pour le revêtement décoratif d'espaces ambiants
US11639316B2 (en) 2018-09-26 2023-05-02 3M Innovative Properties Company Fiber tows with a heat-activated sizing
WO2023152355A1 (fr) * 2022-02-14 2023-08-17 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung eingetragener Verein Film composite pour l'équipement permanent de moules avec une couche de séparation

Also Published As

Publication number Publication date
AU5923399A (en) 2000-04-03
CA2344340A1 (fr) 2000-03-23
BR9913739A (pt) 2001-06-05
AR022093A1 (es) 2002-09-04
EP1127095A1 (fr) 2001-08-29
JP2003525958A (ja) 2003-09-02
EP1127095A4 (fr) 2001-12-12

Similar Documents

Publication Publication Date Title
EP1127095A1 (fr) Revetements en polyurethane pouvant etre reactives par la chaleur et leur utilisation en tant qu'adhesifs
EP1984177B1 (fr) Film de polyester
TWI402167B (zh) 熱可密封之複合聚合性薄膜
TWI252859B (en) Process for the production of coated polymeric film
EP1355005B1 (fr) Procédé de production d'un laminé et articles fabriqués avec un tel revêtement
KR20230134158A (ko) 압출 가공이 가능한 김서림방지 코폴리에스테르 열 밀봉 수지
KR20170134236A (ko) 가열-밀봉 및 박리가능한 폴리에스테르 필름, 그의 용도 및 그의 제조 방법
GB2233251A (en) Production of polymeric films
EP1784467A1 (fr) Pellicules polymères thermocollables
KR20190013604A (ko) 박리가능한 폴리에스테르 필름, 그의 용도 및 그의 제조 방법
JPS62222831A (ja) 易劈開性フイルム

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AU BR CA CN ID JP KR SG VN

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
ENP Entry into the national phase

Ref document number: 2344340

Country of ref document: CA

Ref country code: CA

Ref document number: 2344340

Kind code of ref document: A

Format of ref document f/p: F

ENP Entry into the national phase

Ref country code: JP

Ref document number: 2000 570257

Kind code of ref document: A

Format of ref document f/p: F

WWE Wipo information: entry into national phase

Ref document number: 59233/99

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: 1999946931

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: 1999946931

Country of ref document: EP

WWW Wipo information: withdrawn in national office

Ref document number: 1999946931

Country of ref document: EP