EP3105297A1 - Ruban adhesif - Google Patents

Ruban adhesif

Info

Publication number
EP3105297A1
EP3105297A1 EP15704767.1A EP15704767A EP3105297A1 EP 3105297 A1 EP3105297 A1 EP 3105297A1 EP 15704767 A EP15704767 A EP 15704767A EP 3105297 A1 EP3105297 A1 EP 3105297A1
Authority
EP
European Patent Office
Prior art keywords
adhesive tape
adhesive
tape according
previous
film
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
EP15704767.1A
Other languages
German (de)
English (en)
Inventor
Frank Lange
Patrick Kerep
Bernhard MÜSSIG
Tanja URBAN
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Tesa SE
Original Assignee
Tesa SE
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
Application filed by Tesa SE filed Critical Tesa SE
Publication of EP3105297A1 publication Critical patent/EP3105297A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • C09J107/00—Adhesives based on natural rubber
    • 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
    • C09J5/00—Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers
    • 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
    • C09J7/38—Pressure-sensitive adhesives [PSA]
    • C09J7/381—Pressure-sensitive adhesives [PSA] based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C09J7/383—Natural or synthetic rubber
    • 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
    • C09J2301/00—Additional features of adhesives in the form of films or foils
    • C09J2301/30—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
    • C09J2301/312—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier parameters being the characterizing feature
    • 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
    • C09J2407/00—Presence of natural rubber
    • 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
    • C09J2423/04—Presence of homo or copolymers of ethene
    • C09J2423/046—Presence of homo or copolymers of ethene 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
    • C09J2423/00—Presence of polyolefin
    • C09J2423/10—Presence of homo or copolymers of propene
    • C09J2423/106—Presence of homo or copolymers of propene in the substrate

Definitions

  • the invention relates to an adhesive tape.
  • So-called strapping tapes are particularly suitable for bundling objects.
  • Such items are for example tubes, profiles or stacked boxes (strapping application).
  • the strapping applications include the fixation of moving parts on white appliances (such as refrigerators and freezers or air conditioners), on red devices such as (gas) stoves and generally on electrical appliances such as printers.
  • white appliances such as refrigerators and freezers or air conditioners
  • red devices such as (gas) stoves
  • electrical appliances such as printers.
  • Appliance area fixation of moving parts of refrigerators, freezers and other household appliances such as gas stoves etc.
  • unwanted residues of the adhesive tape on the substrate be it in the form of parts of the tape itself or parts of the adhesive.
  • a strapping tape that can be used universally on all substrates relevant to the application, such as the plastics ABS, PS, PP, PE, PC, POM, such as various metals, such as solvent, water-based and applied as a powder paints and other solvent-free paints (for example, UV-curing paints), which at the same time adheres to these substrates with sufficiently high bond strengths of usually at least 2.5 N / cm, but still without residue and damage even after prolonged storage at different temperatures (temperature range: -20 ° C to +60 ° C) and UV irradiation can be removed.
  • substrates relevant to the application such as the plastics ABS, PS, PP, PE, PC, POM, such as various metals, such as solvent, water-based and applied as a powder paints and other solvent-free paints (for example, UV-curing paints)
  • strapping tapes are used in a wide variety of applications, they have some essential properties to meet the particular requirements placed on them. These are - without this list claims to be exhaustive - a very high tensile strength (maximum tensile strength), a very good tensile strength corresponding to a high modulus at low strains and a low elongation at break, a sufficient but not too high bond strength, a metered bond strength on the own rear side, the residue-free redetachability after the stresses of the actual application, the robustness of the wearer opposite mechanical stress and, for some applications, also the resistance of the adhesive tape to UV radiation and to many chemicals.
  • the extensibility and tensile strength are essentially based on the physical properties of the support material used.
  • An adhesive tape which is to be used as a (strapping) adhesive tape should therefore have the following properties:
  • the tape must secure loose parts during transport, ie the tape should have high tear resistance and sufficient bond strength.
  • the tape should not stretch much under load, ie the tape should have high F1 -F10% values (high tensile strength at 1% - and
  • the tape must work under different climatic conditions, ie the tape should have a climatic resistance in the temperature range between -20 ° C to 40 ° C and a relative humidity of up to 95%. ⁇ The tape should be removable in the temperature range between -20 ° C to 40 ° C and a relative humidity of up to 95%.
  • the tape should be heat resistant when drying the adhesive coating in the tape manufacturing process.
  • the adhesive tape should be easy to use, that is, the adhesive tape should preferably have a low unwind force, which can be ensured in particular by using a carbamate or silicone release.
  • the adhesive tape should adhere well to various adhesion reasons and have sufficient cohesion to secure the goods to be transported, ie the adhesive tape may have an adhesive based on natural rubber, SIS rubber or acrylate.
  • the prior art includes tapes, which are used in the field of strapping (bundling), appliance (transport security of moving parts such as drawers, shelves, flaps especially in household appliances, etc.) and in the furniture industry and when used for other applications weaknesses in removing the tape from Substrate in the lower temperature range (below approx. 10 ° C).
  • Biaxially oriented PET films with a thickness of between 30 and 60 ⁇ m.
  • Monoaxially oriented PP films with a thickness between 40 and 150 ⁇ m
  • Biaxially stretched PET supports are known to be advantageous over monoaxially stretched PP supports (MOPP) because of the higher cold cracking resistance, but earlier tear machine direction (MD) than MOPP, are more expensive and colorless in the marketplace.
  • a coloring of the adhesive tape based on a PET film takes place via a subsequent printing process or coloring of the adhesive.
  • Monoaxially stretched PP films are cheaper and easily dyeable (easily recognizable), which is a general requirement for adhesive tapes that are to be removed again. Both types of films are due to the high modulus of elasticity under tensile load in the application little stretchy, so well suited.
  • MOPP strapping tapes are typically used to wrap palletized cartons; the foil does not split when peeled off because the paper easily splits on the surface.
  • MOPP film for surface-protection adhesive tapes if the adhesive adheres so weakly that no adhesive or residual tape with film content remains.
  • an adhesive tape for surface protection applications for example, as a transport lock for PC printers, refrigerators, electric and gas stoves or furniture available, which has a high adhesion, but is residue-free removable and the especially below normal room temperature - for example, between - 20 ° C and +15 ° C.
  • the toughness of a polypropylene film decreases and at the same time the adhesive strength of the adhesive increases. The challenge is to minimize this behavior in the cold and to find a solution to the technical problem by a suitable combination of film and adhesive.
  • the adhesive tape For the functionality of the adhesive tape, the best possible internal strength in the cold of the MOPP support used and the choice of a suitable adhesive are of great importance.
  • the adhesive must enable secure bonding, that is, the bond strengths on the various substrates must not fall below a certain level.
  • the residue-free Wiederablosles the tapes of the different substrates is absolutely necessary, that is, the adhesive must not cohesively fail when peeling off, leave deposits or lead to excessive cracking to splitting or tearing the tape.
  • the object of the invention is to achieve a significant improvement over the prior art and to provide an adhesive tape which has a reduced gap when removing the adhesive tape in the cold at a temperature range between - 20 ° C and up to +15 ° C.
  • the cold gap strength is to be improved in the transverse and z-direction with jerky load on the wearer.
  • an adhesive tape as characterized in detail in the main claim.
  • Advantageous embodiments of the invention are described in the subclaims.
  • the use of the adhesive tape according to the invention is included.
  • the invention relates to an adhesive tape with a support made of a film, to which at least one side an adhesive is applied, wherein the film is a monoaxially stretched film containing at least 50 wt .-% of a polypropylene homopolymer and 10 to 25 wt. %, preferably 12 to 20 wt%, more preferably 15 wt%, of a copolymer of ethylene and 2 to 6 mol% of an ⁇ -olefin, wherein the ⁇ -olefin of the copolymer is a diene having at least four carbon atoms is and is preferably selected from the group butene, hexene and / or octene.
  • the adhesive composition comprises a polyisoprene rubber and one or more tackifier resins wherein the rubber / adhesive resin weight ratio is greater than 1.10.
  • the film of the adhesive tape according to the invention is obtained by extrusion and stretching in the longitudinal direction using conventional, generally known methods.
  • the polypropylene homopolymer used is preferably a granulate which contains only polypropylene as the polymer.
  • the polypropylene homopolymer can also be used in the form of a polypropylene reactor blend.
  • the preparation of such reactor blends is described in EP 0 808 870 A1, EP 0 877 039 A1 and M. Pires et al., J. Appl. Poly. Be. Vol. 92 pp. 2155 to 2162 (2004). They consist of a finely divided, formed during the polymerization mixture of a polypropylene homopolymer and a substantially amorphous ethylene-propylene copolymer (EPR, ethylene propylene rubber).
  • EPR substantially amorphous ethylene-propylene copolymer
  • a reactor blend with a high proportion of the EPR copolymer, ie a proportion of 5 to 12 wt .-% (that is, the flexural modulus of the raw material or the modulus of elasticity of the film are less than 1250 MPa) results in admixture with a copolymer of ethylene and octene, soft films.
  • a polypropylene reactor blend is contained in the film in addition to the pure polypropylene homopolymer and the copolymer of ethylene and octene as the third polymer component.
  • the compatibility of polypropylene and polyethylene is limited (that is, the adhesion of the two phases to each other is poor), therefore, a reactor blend can serve as a compatibilizer in the polymer blend according to the invention and thus improve the mechanical properties.
  • a particularly preferred film contains 55 to 80% by weight of a polypropylene homopolymer, 10 to 25% by weight (preferably 15% by weight) of a copolymer of ethylene and octene according to the invention and 10 to 20% by weight (preferably 15% by weight). -%) of an EPR.
  • the EPR can in addition to the invention Main ingredients are also added as an independent raw material, examples of trade names are Vistamaxx® and Versify®.
  • Another particularly preferred film contains 75 to 90% by weight of a polypropylene impact copolymer, 10 to 25% by weight (preferably 15% by weight) of a copolymer of ethylene and octene according to the invention.
  • the EPR is preferably used as part of a polypropylene reactor blend.
  • Polypropylene random copolymers are also suitable as compatibilizers for the main components according to the invention, but disadvantageous because of their lower heat stability during coating with the adhesive.
  • the film according to the invention also essentially consists of a homopolymer or a polypropylene impact copolymer and not of a random copolymer.
  • the melt index of the polypropylene of the invention (230 ° C) is preferably in the range of 0.5 to 5 dg / min (g / 10 min) and crystallite melting point at least 158 ° C and the flexural modulus preferably at least 1400 MPa.
  • the copolymer of ethylene and octene preferably has a melt index of 0.5 to 5 dg / min (190 ° C) and preferably a density of 0.895 to 0.925 g / cm 3 .
  • the ethylene copolymer may also be an ⁇ -olefin having four, five, six, seven, nine and more carbon atoms.
  • the ⁇ -olefin of the copolymer is not propylene (having three carbon atoms) because such mixtures on stripping lead to carrier cleavage, presumably due to the significantly higher glass transition temperature than the copolymers of the present invention.
  • the film may also be added to PE and PP based masterbatches such as PM2979E4 from Techmer PM.
  • Masterbatch or color granules are plastic additives in the form of granules with levels of colorants or additives that are higher than in the end use. They are added to the natural plastic (raw polymer) for coloring or for changing the properties. Masterbatches increase process reliability compared to pastes, powders or liquid additives and are very easy to process.
  • the stretch ratio in the stretching of the extruded primary film in the longitudinal direction (machine direction) is preferably 1: 5 to 1: 9, particularly preferably 1: 6 to 1: 7.5, very particularly preferably 1: 6 to 1: 6.5.
  • a stretch ratio of 1: 6 indicates that a section of 6 m length of the stretched film is formed from a section of the film of, for example, 1 m in length.
  • the stretching takes place without the width of the primary film substantially decreasing, solely at the expense of the thickness of the film.
  • the usual film thickness after stretching is between 40 and 150 ⁇ . Preference is given to 50 to 100 ⁇ .
  • At least one corona or else flame pretreatment of the side of the film carrier to be coated later with the adhesive takes place in order to better anchor the adhesive to the carrier.
  • a further improvement in adhesion equivalent to the anchoring of the adhesive on the support can be achieved by the use of primers.
  • the surface energy can be adjusted in a targeted manner and, on the other hand, for example when using isocyanate-containing primers, a chemical attachment of the elastomeric adhesive component to the carrier can be pursued.
  • the usual surface application weight of the primer is between 0.1 and 10 g / m 2 .
  • Another way to improve the anchoring is the use of carrier films, which are equipped by coextrusion at the film manufacturer specifically with a favorable for the connection to the pressure sensitive adhesive polymer surface.
  • the adhesive according to the invention contains a polyisoprene rubber and one or more adhesive resins, the rubber / adhesive resin weight ratio being greater than 1.10.
  • the rubber / adhesive resin weight ratio is between 1.10 and 1.60, preferably between 1.30 and 1.50.
  • Preferred polyisoprene rubber is natural rubber. Its Mooney viscosity (conditions 1 + 4, 125 ° C) is preferably between 50 and 110, more preferably between 55 and 75, more preferably at 75.
  • the adhesive consists only of rubber and tackifier resins, more preferably only of rubber and tackifier resins, with up to 20 % By weight (based on the total composition) of anti-aging agents.
  • the adhesive consists only of polyisoprene rubber as the elastomer component, more preferably only of natural rubber, to which (in addition to the tackifier resins) the customary and known additives can be added.
  • an adhesive is used whose elastomer consists of the group of natural rubbers or a blend of natural rubbers and / or synthetic rubbers, wherein the proportion of the synthetic rubber in the blend according to a preferred variant is at most as large as the proportion of natural rubber.
  • the natural rubber or natural rubbers can in principle be made of all available grades such as Crepe, RSS, ADS, TSR or CV grades, depending on the required level of purity and viscosity, and the synthetic rubber or synthetic rubbers from the group of random copolymerized Styrene butadiene rubbers (SBR), butadiene rubbers (BR), synthetic polyisoprenes (IR), butyl rubbers (II FR), halogenated butyl rubbers (XIIR), acrylate rubbers (ACM), ethylene Vinyl acetate copolymers (EVA) and the polyurethanes and / or their blends are selected.
  • SBR Styrene butadiene rubbers
  • BR butadiene rubbers
  • IR butyl rubbers
  • XIIR halogenated butyl rubbers
  • ACM ethylene Vinyl acetate copolymers
  • EVA ethylene Vinyl acetate copolymers
  • thermoplastic elastomers in a weight proportion of 10 to 20% by weight, based on the total elastomer content.
  • SIS styrene-isoprene-styrene
  • SBS styrene-butadiene-styrene
  • Rubber adhesives show a good combination of bond strength, tack and cohesion as well as balanced adhesion on almost all relevant substrates and are thus predestined.
  • General information on rubber adhesives can be found, inter alia, in standard works for adhesive tapes such as, for example, the "Handbook of Pressure Sensitive Adhesive Technology" by Donatas Satas.
  • hydrogenated and nonhydrogenated hydrocarbon resins and polyterpene resins can be used as adhesive resins in the (self) adhesive, for example as main component.
  • Unhydrogenated hydrocarbon resins and rosin-based adhesive resins can also be used.
  • Can an adjustment of the T g s of the relationship of resins of high softening point can be controlled to resins having low softening point by using different adhesive resins having different softening points, in addition to K / H ratio.
  • tackifier resin the skilled person understands a resin-based substance which increases the tackiness.
  • Preferred resins used are C 5 -hydrocarbon resins.
  • hydrogenated and unhydrogenated hydrocarbon resins and polyterpene resins can be used as adhesive resins in the case of the self-adhesive composition as main component.
  • hydrogenated polymers of dicyclopentadiene for example Escorez 5300 series, Exxon Chemicals
  • hydrogenated polymers of preferably C 8 and C 9 aromatics for example Regalite and Regalrez series, Eastman Inc. or Arkon P series, Arakawa
  • C 8 and C 9 aromatics for example Regalite and Regalrez series, Eastman Inc. or Arkon P series, Arakawa
  • These can flow by hydrogenation of polymers of pure aromatic streams or based by hydrogenation of polymers based on mixtures of different aromatics.
  • partially hydrogenated polymers of C 8 and C 9 aromatics for example Regalite and Regalrez series, Eastman Inc.
  • Arkon M Arakawa
  • hydrogenated polyterpene resins for example Clearon M, Yasuhara
  • hydrogenated C 5 / C 9 Polymers for example, ECR-373, Exxon Chemicals
  • aromatically modified, selectively hydrogenated dicyclopentadiene derivatives e.g., Escorez 5600 series, Exxon Chemicals.
  • the aforementioned adhesive resins can be used both alone and in admixture.
  • Hydrogenated hydrocarbon resins are particularly suitable as a blending component for crosslinkable styrenic block copolymers, as described for example in EP 0 447 855 A1, US Pat. No. 4,133,731 A and US Pat. No. 4,820,746 A, since crosslinking can not be disturbed by the absence of double bonds.
  • non-hydrogenated resins can also be used if crosslinking promoters, such as, for example, polyfunctional acrylates, are used.
  • crosslinking promoters such as, for example, polyfunctional acrylates
  • Other non-hydrogenated hydrocarbon resins, non-hydrogenated analogs of the hydrogenated resins described above may also be used.
  • rosin-based resins for example, foral, foralyn
  • rosin-based resins for example, foral, foralyn
  • the rosins mentioned above include, for example, natural rosin, polymerized rosin, partially hydrogenated rosin, fully hydrogenated rosin, esterified products of these rosins (such as glycerol esters, pentaerythritol esters, ethylene glycol esters and methyl esters) and rosin derivatives (such as disproportionating rosin, fumaric acid-modified rosin, and lime modified rosin).
  • the tackifier resins from bio-based raw materials are polyterpene resins based on ⁇ -pinene and / or ⁇ -pinene and / or ⁇ -lime or terpene-phenolic resins.
  • the amount by weight of the resins is at most 90.91 (more specifically, 100/1, 1) phr (that is, 100 parts by weight of isoprene rubber), preferably 60 to 90 phr.
  • the adhesive may be added to stabilize conventional additives such as anti-aging agents (antiozonants, antioxidants, sunscreens, etc.).
  • additives to the adhesive are typically used:
  • Plasticizers such as plasticizer oils or low molecular weight liquid polymers such as low molecular weight
  • secondary antioxidants such as phosphites or thiosynergists (thioethers)
  • correspondingly useful elastomers include, but are not limited to, those based on pure hydrocarbons, for example, unsaturated polydienes such as natural or synthetically produced polyisoprene or polybutadiene, chemically substantially saturated elastomers such as saturated ethylene-propylene copolymers, ⁇ -olefin copolymers, polyisobutylene, butyl rubber, ethylene Propylene rubber, as well as chemically functionalized hydrocarbons such as halogen-containing, acrylate-containing, allyl or vinyl ether-containing polyolefins
  • unsaturated polydienes such as natural or synthetically produced polyisoprene or polybutadiene
  • chemically substantially saturated elastomers such as saturated ethylene-propylene copolymers, ⁇ -olefin copolymers, polyisobutylene, butyl rubber, ethylene Propylene rubber, as well as chemically functionalized hydrocarbons such as halogen-containing, acrylate-containing
  • Fillers such as fibers, carbon black, zinc oxide, titanium dioxide, micro-solid spheres, solid or hollow glass spheres, silica, silicates, chalk
  • the adhesive in conjunction with said film allows in the range of the usual application temperature, which is between - 20 ° C and + 40 ° C, a residue-free peeling.
  • the usual surface application weight of the dry adhesive is between 10 and 50 g / m 2 , preferably between 20 and 40 g / m 2 . According to the invention, it can be shown that with the increase of the rubber / adhesive resin weight ratio, which leads to a reduction of the dynamic T g s within the adhesive, a reduction of the carrier crevice during cold stripping can be achieved. Although the bond strengths are reduced compared to the adhesive tapes known from the prior art, this reduction is not so strong that a sufficiently good bond strength is no longer present. This is shown in FIG. 1.
  • the upper curve shows the bond strengths measured at different temperatures on polystyrene of a standard strapping adhesive tape with a dynamic T g at 10 rad / s of the adhesive of +6 ° C. at a K / H ratio of 0.89 (rounded up to 0.90).
  • the carrier used corresponds to the carrier film 1 described in the examples.
  • the lower curve shows the bond strengths on polystyrene of an adhesive tape according to the invention at different test temperatures.
  • the adhesive has a dynamic T g at 10 rad / s of -12 ° C at a K / H ratio of 1.4.
  • the carrier used corresponds to the carrier film 1 described in the examples.
  • the K / H ratio should be 1, 1 or more, which is shown in FIG. Due to this K / H ratio, the dynamic T g of the adhesive is lowered, which significantly reduces the splitting of the adhesive tape when polystyrene is peeled off in the cold and is therefore significantly above the previously known level in the inventive sense.
  • FIG. 4 shows the same situation with respect to T g s.
  • a K / H ratio of 0.85 corresponds to a dynamic T g of 6.8 ° C
  • a K H ratio of 1.1 corresponds to a dynamic T g of -3.6 ° C
  • a K / H ratio of 1, 3 corresponds to a dynamic T g of -9 ° C
  • a K / H ratio of 1, 4 corresponds to a dynamic T g of -12 ° C.
  • adheresive tape encompasses all flat structures such as films or film sections which are expanded in two dimensions, tapes of extended length and limited width, strip sections and the like, and ultimately also diecuts or labels.
  • the adhesive tape can be rolled up on itself in the form of a roll, that is to say in the form of an Archimedean spiral, and also produced with adhesive materials such as siliconized paper or siliconized film.
  • a backside lacquer can be applied to favorably influence the unwinding properties of the adhesive tape wound on the Archimedean spiral.
  • This backcoat can be equipped with silicone or fluorosilicone compounds as well as polyvinyl stearyl carbamate, Polyethyleniminstearylcarbamid or fluoroorganic compounds as abhesive (anti-adhesive) acting substances.
  • Suitable release agents include surfactant-release systems based on long-chain alkyl groups such as Stearylsulfosuccinate or Stearylsulfosuccinamate, but also polymers which can be selected from the group consisting of Polyvinylstearylcarbamaten, Polyethyleniminstearylcarbamiden, chromium complexes of CM to C 2 8 fatty acids and stearyl copolymers as For example, in DE 28 45 541 A are described. Also suitable are release agents based on acrylic polymers with perfluorinated alkyl groups, silicones or fluorosilicone compounds, for example based on poly (dimethyl-siloxanes).
  • the release layer comprises a silicone-based polymer.
  • Particularly preferred examples of such separating effective Silicone-based polymers comprise polyurethane- and / or polyurea-modified silicones, preferably organopolysiloxane / polyurea / polyurethane block copolymers, particularly preferably those as described in Example 19 of EP 1 336 683 B1, very particularly preferably anionically stabilized polyurethane- and urea-modified silicones with a silicone rubber. Weight fraction of 70% and an acid number of 30 mg KOH / g.
  • the use of polyurethane and / or urea-modified silicones causes the effect that the products according to the invention have an optimized separation behavior with optimized aging resistance and universal compatibility.
  • the release layer comprises 10 to 20% by weight, particularly preferably 13 to 18% by weight, of the release-active constituent.
  • Inventive adhesive tapes are preferably used in the widths of 9 to 50 mm, in particular 19 to 25 mm and have a preferred thickness of 40 to 200 ⁇ , preferably 70 to 180 ⁇ , more preferably 75 to 120 ⁇ .
  • FIG. 5 shows a typical structure of the adhesive tape according to the invention.
  • the product consists of a film (a) and an adhesive (b).
  • a primer for improving the adhesion between the adhesive and the backing and a reverse side release (d).
  • the carrier (a) consists of a monoaxially oriented polypropylene film with a preferred thickness between 30 and 150 ⁇ .
  • the adhesive (b) is a mixture of natural rubber or other elastomers and various resins and may optionally also contain plasticizers, fillers and anti-aging agents.
  • the formulation of the adhesive is adjusted so that the ratio of elastomer / resin is chosen so that the T g of the total mixture is in the range of application temperature or even below the minimum application temperature. Further lowering of the T g by suitable plasticizers or low T g resins is possible.
  • the preparation and processing of the PSAs can be carried out from solution, dispersion and from the melt.
  • Preferred production and processing methods are carried out from solution as well as from the melt.
  • Particularly preferred is the production of Melt adhesive from the melt, in particular batch or continuous processes can be used.
  • Particularly advantageous is the continuous production of the PSAs by means of an extruder.
  • the pressure-sensitive adhesives prepared in this way can then be applied to the carrier by the generally known methods. When processed from the melt, these can be application methods via a nozzle or a calender.
  • the adhesive tape of the invention shows a good Wiederablos Hampshire of a variety of substrates at temperatures of up to - 20 ° C.
  • the reversibility is also given at positive temperatures (+40 ° C), that is, there are no residues due to cohesive failure of the adhesive, Masseumspulen (poor ground anchorage) or a carrier column to observe.
  • the carrier has a sufficient internal strength in all three spatial directions and high impact resistance even in the cold.
  • FIG. 6 shows in detail the results of various patterns.
  • Examples 1 and 4 with a K / H ratio of 0.92 are not comparative examples according to the invention.
  • the support When removing the adhesive tape produced therewith, the support fails at least occasionally even at comparatively high temperatures of 0 ° C., while at -20 ° C. an almost complete gap can be observed in all cases.
  • the adhesive tape can be excellently used as a strapping adhesive tape for bundling and palletizing cardboard boxes and other goods, even at low temperatures.
  • the adhesive tape according to the invention can also be used advantageously in the following applications:
  • PE 6 wt.% By weight PE and with 3 wt.% By weight of an n-heptane-soluble constituent of an ethylene-propylene copolymer (EPR)
  • Carrier film 1
  • a film of a total thickness of about 550 ⁇ m and a width of 1400 mm is extruded onto a chill roll via a slot die.
  • This primary film is fed via preheat rollers to a roll erector of conventional design and stretched at temperatures of 100 ° C to 135 ° C in the ratio 1: 6.5 along.
  • the resulting film has a thickness of 85 ⁇ and after edge trimming a width of 1200 mm.
  • Carrier film 2
  • Carrier production such as carrier film 1.
  • a commercial carbamate varnish from the class of polyvinyl stearyl carbamates having a melting point between 85 ° C and 1 10 ° C is applied.
  • the separating substance is applied as a 2% solution in toluene with a roller applicator and then dried.
  • the coating thickness (dry) is 0.05 g / m 2 .
  • a commercially available silicone release varnish from the class of condensation-crosslinking two-component systems or an addition-crosslinking silicone system can be applied.
  • the separating substance is applied as a 5% solution in toluene with a roller applicator.
  • the coating thickness (dry) is 0.15 g / m 2 .
  • a prior art primer is applied on the corona-pretreated surface of the second side.
  • the pressure-sensitive adhesive is applied to the primer.
  • the adhesive is applied as a 30% solution in gasoline followed by drying.
  • the glue application is 25 g / m 2 .
  • the order from the melt is possible.
  • the coated carrier webs are cut on special cutting machines to 19 mm wide and 66 m long rolls and wound up. Test Methods
  • the measurements are (unless otherwise stated) at a test climate of 23 ⁇ 1 ° C and 50 ⁇ 5% rel. Humidity carried out.
  • the determination of the bond strength is carried out as follows.
  • a defined primer galvanized sheet steel with a thickness of 2 mm (supplied by Rocholl GmbH) is used.
  • the glued surface element to be examined is cut to a width of 20 mm and a length of about 25 cm, provided with a handling section and immediately thereafter pressed five times with a steel roller of 4 kg at a feed rate of 10 m / min on the selected primer.
  • the measured value (in N / cm) is the average of three individual measurements.
  • amorphous or partially crystalline systems are characterized by the transformation of the more or less hard amorphous or partially crystalline phase into a softer (rubbery to viscous) phase.
  • "thawing” or “freezing” upon cooling) of the Brownian motion of longer chain segments occurs.
  • the glass transition temperature can be given as dynamic or as static glass transition temperature depending on its measurement.
  • the dynamic glass transition temperature data in this disclosure refers to determination by dynamic mechanical analysis (DMA) at a low frequency (temperature sweep, measuring frequency: 10 rad / s, temperature range: -35 ° C to 80 ° C, heating rate: 2) , 5 ° C / min; Rheometric Scientific DSR I; parallel plate assembly, measuring head 200 g air-bearing with normal force; temperature control: Peltier element; sample thickness 1 mm: sample diameter 25 mm: preload with a load of 3N; stress of the samples in all measurements 2500 Pa).
  • DMA dynamic mechanical analysis
  • the glass transition temperature corresponds to the temperature at which the loss factor (tanö) has its maximum.
  • the glued test panels are stored under defined test conditions in the heating cabinet (1 d at 43 ° C), so that a sufficiently good wetting of the primer can be done with the adhesive. Afterwards, the test plates are brought directly from the drying oven into a walk - in climate chamber at - 10 ° C and stored there for another 24 h. After 24 hours, the actual extraction test in the walk-in climate chamber is carried out at the respective selected withdrawal temperature (0 ° C, -5 ° C, -10 ° C and -20 ° C).
  • the bonded adhesive tape strips are peeled off from the primer under a peel angle of successively 90 ° and then 180 ° and a drawing speed of initially 0.3 m / min and then 30 m / min.
  • melt flow index "Melt Flow Ratio" is measured according to ISO 1 133. For polyethylenes this is determined at 190 ° C and a weight of 2.16 kg, for polypropylenes at a temperature of 230 ° C.
  • the crystallite melting point is determined as usual according to ISO 3146 with DSC and a heating rate of 10 K / min.
  • the density is measured according to ASTM D 792.
  • the adhesive resin softening temperature is carried out according to the relevant method known as Ring and Ball, which is standardized according to ASTM E28.
  • a Ring-Kugel-Automat HRB 754 from Herzog is used to determine the adhesive resin softening temperature of the resins. Resin samples are first finely ground. The resulting powder is placed in a brass cylinder with bottom opening (inner diameter at the upper part of the cylinder 20 mm, diameter of the bottom opening of the cylinder 16 mm, height of the cylinder 6 mm) and melted on a heating table. The filling amount is chosen so that the resin after melting completely fills the cylinder without supernatant. The resulting specimen, including the cylinder, is inserted in the sample holder of the HRB 754. Glycerol is used to fill the tempering bath, provided that the adhesive resin softening temperature is between 50 ° C and 150 ° C.
  • the test balls have a diameter of 9.5 mm and weigh 3.5 g.
  • the ball is placed above the specimen in the temperature control bath and deposited on the specimen. 25 mm below the cylinder bottom there is a catch plate, 2 mm above this a light barrier.
  • the temperature is increased at 5 ° C / min.
  • the ball begins to move through the bottom opening of the cylinder until it eventually stops on the catch plate. In this position, it is detected by the photocell and registered at this time, the temperature of the bath. There is a double determination.
  • the adhesive resin softening temperature is the average of the two individual measurements.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Adhesive Tapes (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

Ruban adhésif qui comporte un support constitué d'une feuille sur au moins une face de laquelle est appliquée une colle, ladite feuille étant une feuille monoaxialement étirée, constituée d'au moins 50 % en poids d'un homopolymère de polypropylène et de 10 à 25 % en poids, de préférence de 15 %, d'un copolymère d'éthylène et de 2 à 6 % en moles d'une α-oléfine. Ladite α-oléfine est une diène ayant au moins quatre atomes de carbone, et la colle contient un caoutchouc polyisopropylène et une ou plusieurs résines adhésives, le rapport pondéral caoutchouc/résine adhésive étant supérieur à 1,10.
EP15704767.1A 2014-02-10 2015-02-09 Ruban adhesif Withdrawn EP3105297A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102014202341 2014-02-10
PCT/EP2015/052595 WO2015118138A1 (fr) 2014-02-10 2015-02-09 Ruban adhesif

Publications (1)

Publication Number Publication Date
EP3105297A1 true EP3105297A1 (fr) 2016-12-21

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Application Number Title Priority Date Filing Date
EP15704767.1A Withdrawn EP3105297A1 (fr) 2014-02-10 2015-02-09 Ruban adhesif

Country Status (7)

Country Link
US (1) US20160355707A1 (fr)
EP (1) EP3105297A1 (fr)
JP (1) JP6503378B2 (fr)
KR (1) KR20160121559A (fr)
CN (1) CN106062112B (fr)
CA (1) CA2937602A1 (fr)
WO (1) WO2015118138A1 (fr)

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DE102017203066A1 (de) * 2017-02-24 2018-08-30 tesa SE, Kst. 9500 - Bf. 645 Klebeband
DE102017203068A1 (de) * 2017-02-24 2018-08-30 Tesa Se Klebeband
DE202017003329U1 (de) * 2017-06-26 2018-09-27 Tesa Se Klebeband und Folie
KR200492161Y1 (ko) * 2018-08-20 2020-08-20 테사 소시에타스 유로파에아 접착 테이프
KR200493725Y1 (ko) * 2018-08-20 2021-05-25 테사 소시에타스 유로파에아 접착 테이프

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DK0544098T3 (da) * 1991-11-27 1999-05-17 Mitsubishi Chem Corp Polyolefinbaseret emballagefolie
DE19718900A1 (de) * 1997-05-05 1998-11-12 Targor Gmbh Polypropylen Formmasse mit ausgezeichneter Steifigkeits-Zähigkeitsrelation
DE19939076A1 (de) * 1999-08-18 2001-02-22 Beiersdorf Ag Verpackungsklebeband mit Naturkautschuk-Schmelzhaftkleber
DE10036705A1 (de) * 2000-07-27 2002-03-28 Tesa Ag Klebeband insbesondere zu Verpackungszwecken
JP4271388B2 (ja) * 2001-07-16 2009-06-03 株式会社日立プラントテクノロジー トラフ式自動スカムスキマ
JP4737655B2 (ja) * 2002-05-24 2011-08-03 大日本印刷株式会社 金属接着用介在フィルム
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DE102008005564A1 (de) * 2008-01-22 2009-07-23 Tesa Ag Trägerfolie insbesondere für ein Klebeband und Verwendung derselben
DE102008005565A1 (de) * 2008-01-22 2009-07-23 Tesa Ag Folie aus Polypropylen, Verwendung derselben sowie Verfahren zur Herstellung der Folie
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JP5916386B2 (ja) * 2009-07-03 2016-05-11 三井化学株式会社 表面保護フィルム
JP5598334B2 (ja) * 2011-01-07 2014-10-01 王子ホールディングス株式会社 粘着テープ
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Also Published As

Publication number Publication date
JP2017508057A (ja) 2017-03-23
CA2937602A1 (fr) 2015-08-13
CN106062112A (zh) 2016-10-26
WO2015118138A1 (fr) 2015-08-13
JP6503378B2 (ja) 2019-04-17
CN106062112B (zh) 2019-09-17
US20160355707A1 (en) 2016-12-08
KR20160121559A (ko) 2016-10-19

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