EP4055110A1 - Couche de masse adhésive expansée et ruban adhésif comprenant la couche de masse adhésive expansée - Google Patents

Couche de masse adhésive expansée et ruban adhésif comprenant la couche de masse adhésive expansée

Info

Publication number
EP4055110A1
EP4055110A1 EP20800890.4A EP20800890A EP4055110A1 EP 4055110 A1 EP4055110 A1 EP 4055110A1 EP 20800890 A EP20800890 A EP 20800890A EP 4055110 A1 EP4055110 A1 EP 4055110A1
Authority
EP
European Patent Office
Prior art keywords
weight
adhesive
pressure
layer
sensitive adhesive
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.)
Pending
Application number
EP20800890.4A
Other languages
German (de)
English (en)
Inventor
Thilo Dollase
Michael Egger
Aranzazu Escudero Vallejo
Jessika Gargiulo
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 EP4055110A1 publication Critical patent/EP4055110A1/fr
Pending legal-status Critical Current

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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
    • C09J153/00—Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
    • C09J153/02—Vinyl aromatic monomers and conjugated dienes
    • 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
    • C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/32—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof from compositions containing microballoons, e.g. syntactic foams
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L53/02—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
    • 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
    • C09J193/00—Adhesives based on natural resins; Adhesives based on derivatives thereof
    • C09J193/04—Rosin
    • 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
    • C09J7/10—Adhesives in the form of films or foils without carriers
    • 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
    • C09J7/387—Block-copolymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00—Applications
    • C08L2203/14—Applications used for foams
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00—Applications
    • C08L2203/20—Applications use in electrical or conductive gadgets
    • C08L2203/206—Applications use in electrical or conductive gadgets use in coating or encapsulating of electronic parts
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00—Polymer mixtures characterised by other features
    • C08L2205/14—Polymer mixtures characterised by other features containing polymeric additives characterised by shape
    • C08L2205/18—Spheres
    • C08L2205/20—Hollow spheres
    • 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
    • C09J2301/10—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
    • C09J2301/12—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers
    • C09J2301/124—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers the adhesive layer being present on both sides of the carrier, e.g. double-sided adhesive tape
    • 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
    • C09J2301/302—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 the adhesive being pressure-sensitive, i.e. tacky at temperatures inferior to 30°C
    • 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
    • C09J2301/308—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 the adhesive tape or sheet losing adhesive strength when being stretched, e.g. stretch adhesive
    • 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
    • C09J2301/40—Additional features of adhesives in the form of films or foils characterized by the presence of essential components
    • C09J2301/412—Additional features of adhesives in the form of films or foils characterized by the presence of essential components presence of microspheres
    • 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
    • C09J2400/00—Presence of inorganic and organic materials
    • C09J2400/20—Presence of organic materials
    • C09J2400/24—Presence of a foam
    • 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
    • C09J2453/00—Presence of block copolymer
    • 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
    • C09J2493/00—Presence of natural resin

Definitions

  • the invention relates to foamable PSAs, foamed PSA layers, self-adhesive products containing them such as, in particular, adhesive tapes, and the use of double-sided adhesive variants of the adhesive tapes in a composite with two substrates such as components of mobile devices.
  • Synthetic rubber-based PSAs which contain styrene block copolymers are well known and are used in a wide variety of applications. Advantages of this type of PSA are the high bond strength on substrates of different surface energy and, above all, on substrates with low surface energy. At the same time, they impress with their very high holding power under normal ambient conditions.
  • mobile devices includes, for example, devices of the consumer electronics industry, which include electronic, optical and precision mechanical devices, in the sense of this application in particular devices as they are in class 9 of the international classification of goods and services for the registration of Brands (Classification of Nice), 10th edition (NCL (10-2013)), if they are electronic, optical or precision mechanical devices, clocks and timekeeping devices according to class 14 (NCL (10-2013)) are still to be classified, like in particular
  • Solar cell modules such as electrochemical dye solar cells, organic solar cells, thin-film cells,
  • adhesive tapes in particular are required that have a high holding capacity. In some cases, there is also a desire for later removability. In many applications, high strength is also required at elevated temperatures.
  • the adhesive tapes do not fail in their holding capacity if the mobile device, for example a cell phone, is dropped and hits the ground.
  • the adhesive strip or the adhesive bond must therefore have a very high shock resistance.
  • Pressure-sensitive adhesives based on styrene block copolymers are among the classic adhesive families used in self-adhesive products. A number of technological aspects relating to such PSAs are described, for example, by D. Satas (FC Jagisch, JM Tancrede in Handbook of Pressure Sensitive Adhesive Technology, D. Satas (ed.), 3rd edition!., 1999, Satas & Associates, Warwick , Rhode Island, chapter 16).
  • EP 3 075 775 A1 describes foamed block copolymer coatings with adhesive resin (combinations).
  • adhesive resin for example, hydrocarbon and polyterpene resins, oxygen-containing adhesive resins can be used, but these are not specified further.
  • DE 10 2008 056 980 A1 and DE 10 2008 004 388 A1 teach formulations made tacky with adhesive resins and disclose a formulation which, inter alia, contains a polystyrene-polyisoprene block copolymer and, for example, a rosin ester.
  • the adhesives contain a relatively high proportion of microballoons, which accordingly leads to very low densities.
  • the invention relates to a foamable pressure-sensitive adhesive, in particular for double-sided self-adhesive tapes, comprising a) 41.7% by weight to 62.0% by weight of an elastomer component, b) 37.7% by weight to 58.0% by weight % of an adhesive resin component, c) 0% by weight to 15% by weight of a soft resin component, d) 0% by weight to 18% by weight of further additives and e) expandable, ie in particular unexpanded, microballoons with a proportion of preferably 0.3% by weight to 2.5% by weight, more preferably 0.5 % By weight to 2.0% by weight and very preferably 0.7% by weight to 1.7% by weight, at least 90% by weight of the elastomer component (a) being composed of polyvinylaromatic-polydiene block copolymers and wherein the adhesive resin component (b) contains from 4% by weight to 100% by weight (based on the adhesive resin component) at least one type K1 of
  • the invention also relates to a foamed pressure-sensitive adhesive layer, in particular for double-sided self-adhesive tapes, comprising a) 41.7% by weight to 62.0% by weight of an elastomer component, b) 37.7% by weight to 58.0% by weight % of an adhesive resin component, c) 0% by weight to 15% by weight of a soft resin component, d) 0% by weight to 18% by weight of further additives and e) microballoons with a proportion of preferably 0.3% by weight % to 2.5% by weight, more preferably 0.5% by weight to 2.0% by weight and very preferably 0.7% by weight to 1.7% by weight, the microballoons at least partially are expanded, the elastomer component (a) consisting of at least 90 wt .-% of polyvinylaromatic-polydiene block copolymer, the adhesive resin component (b) from 4% by weight to 100% by weight (based on the adhesive resin component) at least one Type K1 of
  • the further claims relate, in particular, to double-sided adhesive tapes comprising at least one pressure-sensitive adhesive layer according to the invention, to composites in which two substrates are bonded by means of such an adhesive tape, and to the Use of such an adhesive tape for bonding components of mobile devices, such as batteries.
  • a component can be a single chemical compound or a single material or a mixture of several chemical compounds or materials.
  • a pressure-sensitive adhesive is an adhesive which allows a permanent bond with almost all substrates even under relatively light pressure and, if necessary, can be removed again from the substrate after use, essentially without leaving any residue.
  • a pressure-sensitive adhesive has a permanent pressure-sensitive adhesive effect at room temperature, that is to say has a sufficiently low viscosity and high tack, so that it wets the surface of the respective adhesive base even when there is little pressure.
  • the bondability of the adhesive is based on its adhesive properties and the redetachability on its cohesive properties. According to the invention, the terms “pressure-sensitive adhesive” and “self-adhesive” (or terms derived therefrom) are used synonymously.
  • Foamed pressure-sensitive adhesive layers according to the invention have improved shock resistance compared to a reference pressure-sensitive adhesive layer which does not contain any rosin oligomer according to the invention in the adhesive resin component, but is otherwise the same with regard to composition, degree of foaming and self-adhesive tape pattern structure.
  • the shock resistance is preferably improved by more than 10%, very preferably by more than 20%.
  • PSA layers of the invention are particularly attractive if they meet the criteria for bond strength and shock resistance (shock resistance) listed in the following catalog of requirements.
  • PSA layers according to the invention preferably meet all three criteria of the following catalog of requirements as described in Table 1:
  • the elastomer component (a) consists of at least 90% by weight, such as, for example, essentially, of polyvinylaromatic-polydiene block copolymer.
  • the elastomer component typically contains at least one synthetic rubber in the form of a block copolymer with a structure ABA, (AB) n , (AB) n X or (ABA) n X, in which
  • the blocks B independently of one another for a polymer formed by the polymerization of conjugated dienes having 4 to 18 carbon atoms;
  • all synthetic rubbers of the pressure-sensitive adhesive (layer) of the invention can be block copolymers with a structure as set out above.
  • the pressure-sensitive adhesive (layer) of the invention can thus also contain mixtures of different block copolymers with a structure as above.
  • the at least one suitable block copolymer thus typically comprises one or more rubber-like blocks B (soft blocks) and at least two glass-like blocks A (Hard blocks).
  • At least one synthetic rubber of the foamable PSA or foamed PSA layer of the invention is particularly preferably a block copolymer with a structure ABA, (AB) 2 X, (AB) 3 X or (AB) 4 X, where A, B and X are as defined above .
  • All synthetic rubbers of the PSA (layer) block copolymers according to the invention can have a structure ABA, (AB) 2X, (AB) sX or (AB) 4X, A, B and X having the above meanings.
  • the elastomer component can also contain one or more diblock copolymers AB.
  • the synthetic rubber of the pressure-sensitive adhesive (layer) of the invention is a mixture of block copolymers with a structure AB, ABA, (AB) sX or (AB) 4X, which preferably contains at least diblock copolymers AB and / or triblock copolymers ABA.
  • a mixture of diblock and T riblock copolymers and (AB) n or (AB) n X block copolymers with n greater than or equal to 3 is also advantageous.
  • PSAs or PSA layers typically found are those based on block copolymers comprising polymer blocks predominantly formed by vinyl aromatics (A blocks), preferably styrene, and those predominantly formed by the polymerization of 1,3-dienes (B blocks) such as butadiene and isoprene or a copolymer from these applications.
  • a blocks vinyl aromatics
  • B blocks 1,3-dienes
  • the block copolymers of the PSAs or PSA layers preferably have polystyrene end blocks.
  • the block copolymers resulting from the A and B blocks can contain the same or different B blocks.
  • the block copolymers can therefore have linear A-B-A structures.
  • block copolymers of radial shape as well as star-shaped and linear multiblock copolymers can also be used.
  • polymer blocks based on other aromatics-containing homopolymers and copolymers preferably Cs to C12 aromatics
  • vinyl aromatics such as a-methylstyrene-containing aromatic blocks. It can also contain the same or different A blocks.
  • Vinyl aromatics for building up block A preferably include styrene, ⁇ -methylstyrene and / or other styrene derivatives. The block A can thus be present as a homo- or copolymer.
  • Block A is particularly preferably a polystyrene.
  • Preferred conjugated dienes as monomers for the soft block B are in particular selected from the group consisting of butadiene, isoprene, ethylbutadiene, phenylbutadiene, piperylene, pentadiene, hexadiene, ethylhexadiene and dimethylbutadiene and any mixtures of these monomers.
  • Block B can also be present as a homopolymer or as a copolymer.
  • the conjugated dienes are particularly preferred as monomers for the soft block B selected from butadiene and isoprene.
  • the soft block B is a polyisoprene or a polybutadiene or a polymer made from a mixture of butadiene and isoprene.
  • Block B is very particularly preferably a polybutadiene.
  • a blocks are also referred to as “hard blocks” in the context of this invention.
  • B-blocks are also called “soft blocks” or “elastomer blocks”. This reflects the selection according to the invention of the blocks according to their glass transition temperatures (for A blocks at least 25 ° C., in particular at least 50 ° C., and for B blocks, at most 25 ° C., in particular at most -25 ° C.). These details relate to the pure, unmixed block copolymers and can be determined, for example, by means of DSC (Test IV).
  • the proportion of hard block in the block copolymers is at least 12% by weight and at most 40% by weight, preferably at least 15% by weight and at most 35% by weight and, in particular, very preferably in the case of polybutadiene-containing block copolymers at least 20% by weight.
  • a linear tri- or multiblock copolymer preferably has a peak molar mass according to test V (i) of at least 100,000 g / mol or even at least 125,000 g / mol.
  • a radial or star-shaped block copolymer preferably has a peak molar mass according to test V (i) of at least 150,000 g / mol or even at least 200,000 g / mol. ok
  • a diblock copolymer preferably has a peak molar mass according to test V (i) of at least 50,000 g / mol or even at least 80,000 g / mol.
  • the proportion of vinyl aromatic block copolymers, in particular styrene block copolymers, based on the total pressure-sensitive adhesive (layer), is at least 42% by weight and at most 55% by weight, more preferably at least 45% by weight and at most 52% by weight. %.
  • Too low a proportion of vinyl aromatic block copolymers has the consequence that the thermal shear strength of the pressure-sensitive adhesive (layer) is relatively low. Too high a proportion of vinyl aromatic block copolymers in turn has the consequence that the pressure-sensitive adhesive (layer) is hardly pressure-sensitive.
  • the block copolymers resulting from the A and B blocks can contain the same or different B blocks in terms of microstructure (relative ratio of the types of monomer linkages possible for polybutadiene or polyisoprene 1, 4-cis, 1, 4-trans, 1, 2 and 3.4; preferred is a 1.4 proportion (cis + trans) of> 75 mol%, very preferably> 85 mol% based on the polydiene blocks and a 1.4 cis proportion of> 40 mol% based on the polydiene blocks, such as can be determined by means of 1 H-NMR spectroscopy) and / or chain length.
  • microstructure relative ratio of the types of monomer linkages possible for polybutadiene or polyisoprene 1, 4-cis, 1, 4-trans, 1, 2 and 3.4; preferred is a 1.4 proportion (cis + trans) of> 75 mol%, very preferably> 85 mol% based on the polydiene blocks and a 1.4 cis proportion of> 40 mol% based on the polyd
  • a high proportion of 1,4-linkage and, in particular, 1,4-cis-linkage of the monomer units in the polydiene blocks leads to a lower glass transition temperature, so that good shock resistance can be achieved even in a cold environment.
  • Polybutadiene is therefore also the preferred type for the B block or B blocks.
  • the foamable PSAs or foamed PSA layers have at least one adhesive resin in order to increase the adhesion in the desired manner.
  • the adhesive resin should be compatible with the elastomer block of the block copolymers.
  • an “adhesive resin” is understood to mean an oligomeric or polymeric resin which increases the adhesion (the tack, the inherent tack) of the PSA in comparison to the PSA containing no adhesive resin but otherwise identical.
  • Adhesive resins are special compounds with a lower molar mass compared to elastomers, usually with a weight-average molecular weight (test Vii) Mw ⁇ 5,000 g / mol.
  • the weight average molecular weight is typically from 400 to less than 5,000 g / mol, preferably from 500 to 2,000 g / mol.
  • the adhesive resin component (b) has at least one type K1 of a rosin oligomer with a softening temperature (Ring & Ball, Test VI) of at least 90 ° C, with a proportion based on the adhesive resin component of at least 4% by weight and a maximum of 100% by weight .-%.
  • the adhesive resin component preferably has at least 5 to 70% by weight, more preferably 10 to 50% by weight and in particular 15 to 40% by weight, such as 20% by weight to 30% by weight, for example a representative of this type of adhesive resin K1.
  • This adhesive resin type K1 can also be used in combination. Too low a softening temperature does not lead to the desired increase in shock resistance.
  • colophony oligomer is typically understood to mean a compound in the molar mass range described above (Mw ⁇ 5,000 g / mol) which contains at least two structural units originating from colophony as structural elements, these being selected in particular from abietic acid, neoabietic acid, palustric acid, dihydroabietic acid, Dehydroabietic acid, pimaric acid, isopimaric acid derivatives of these and mixtures of these.
  • abietic acid neoabietic acid
  • palustric acid dihydroabietic acid
  • Dehydroabietic acid Dehydroabietic acid
  • pimaric acid isopimaric acid derivatives of these and mixtures of these.
  • dimerized compounds and, very advantageously, esters that are two, three, four or more are suitable Contain rosin units.
  • the tackifier resins can be hydrogenated, stabilized or disproportionated.
  • the K1 rosin oligomer preferably has an acid number of at least 100 mg KOH / g, very preferably at least 50 mg KOH / g, for example at least 75% by weight, such as in particular 100% by weight.
  • the adhesive resin component (b) can contain further adhesive resins in addition to the rosin oligomer of the K1 type.
  • the adhesive resin component (b) can, for example, also preferably have at least one type K2 of an adhesive resin that has a DACP (diacetone alcohol cloud point, Test VII) of greater than -20 ° C, preferably greater than 0 ° C, and a softening temperature (Ring & Ball, Test VI) is greater than or equal to 70 ° C, preferably greater than or equal to 100 ° C and at most +140 ° C.
  • the adhesive resin component (b) typically contains up to 96% by weight, preferably at least 30% by weight and at most 95% by weight, more preferably 50 to 90% by weight, even more preferably 60 to 85% by weight % By weight and in particular 70 to 80% by weight of this type of adhesive resin K2.
  • Suitable representatives of the adhesive resin type K2 are non-polar hydrocarbon resins, for example hydrogenated and non-hydrogenated polymers of dicyclopentadiene, non-hydrogenated, partially, selectively or fully hydrogenated hydrocarbon resins based on Cs, C 5 / C 9 or Cg monomer streams and polyterpene resins based on a -Pinene and / or ß-pinene and / or ⁇ -limonene.
  • the abovementioned tackifier resins can be used either alone or as a mixture, the person skilled in the art for polyisoprene block copolymers or polybutadiene block copolymers selecting from type K2 tackifier resins in accordance with current guidelines on compatibility.
  • a publication by C. Donker for example, can be consulted for this purpose (C. Donker, Proceedings of the Pressure Sensitive Tape Council, 2001, pp. 149-164).
  • the proportion of adhesive resin component (b) in the PSA formulation has an effect on the bond strength.
  • the proportion of adhesive resin should therefore not be too low. However, it has been shown that too high a proportion of adhesive resin (s) has a negative influence on the shock resistance.
  • the proportion of adhesive resin component (b), such as in particular K1 + K2 is therefore at least 37.7% by weight and a maximum of 58 in the context of this invention % By weight, preferably at least 45% by weight and at most 55% by weight, in each case in relation to the total pressure-sensitive adhesive or pressure-sensitive adhesive layer.
  • the optionally replaceable soft resin or soft resin mixture is used for the final fine adjustment of the cohesion / adhesion balance. It typically has a softening temperature of ⁇ 30 ° C (* Ring & Ball, Test VI), very preferably it is a soft resin or soft resin mixture with a melt viscosity at 25 ° C and 1 Hz of at least 20 Pa * s, preferably at least 50 Pa * s. The melt viscosity is determined according to test VIII.
  • the soft resin can be a rosin-based or, very preferably, a hydrocarbon or polyterpene-based soft resin.
  • the soft resin or the soft resin mixture is used in relation to the entire adhesive (layer) in a proportion of 0% by weight to 15% by weight, and preferably of at least 2% by weight and at most 10% by weight. Too high a proportion of soft resin leads to a reduction in cohesion, which has a negative effect on the thermal shear strength.
  • plasticizers such as mineral oils are not advantageous for the purposes of this invention, but can also be used. Their proportion in the overall formulation is then preferably below 5% by weight, very preferably such plasticizers are completely dispensed with.
  • a disadvantage of plasticizers of low viscosity is the risk of migration into layers in contact with the pressure-sensitive adhesive layer or residues after any detachment of the self-adhesive tape from an adhesive substrate.
  • protective agents can be added to the foamable PSA or foamed PSA layer.
  • Primary and secondary aging inhibitors, light and UV protection agents and flame retardants may be mentioned here, but also fillers, dyes and pigments.
  • the adhesive (layer) can be colored as desired or white, gray or black. As such or other additional additives can typically be used:
  • Plasticizers such as, for example, low molecular weight liquid polymers, such as, for example, low molecular weight polybutenes, preferably with a proportion of 0.2 to less than 5% by weight based on the total weight of the pressure-sensitive adhesive (layer)
  • Primary antioxidants such as sterically hindered phenols, preferably in a proportion of 0.2 to 1% by weight based on the total weight of the pressure-sensitive adhesive (layer),
  • Secondary antioxidants such as phosphites or thioethers, preferably in a proportion of 0.2 to 1% by weight based on the total weight of the pressure-sensitive adhesive (layer),
  • Process stabilizers such as C radical scavengers, preferably with a proportion of 0.2 to 1% by weight based on the total weight of the pressure-sensitive adhesive (layer),
  • light stabilizers such as UV absorbers or sterically hindered amines, preferably in a proportion of 0.2 to 1% by weight based on the total weight of the pressure-sensitive adhesive (layer),
  • Processing aids preferably in a proportion of 0.2 to 1% by weight based on the total weight of the pressure-sensitive adhesive (layer),
  • End block reinforcement resins if desired, preferably in a proportion of 0.2 to 10% by weight based on the total weight of the pressure-sensitive adhesive (layer) and
  • elastomeric nature include those based on pure hydrocarbons, for example unsaturated polydienes such as natural or synthetic polyisoprene or polybutadiene, chemically essentially saturated elastomers such as saturated ethylene-propylene copolymers, ⁇ -olefin copolymers, polyisobutylene, butyl rubber, ethylene Propylene rubber and chemically functionalized hydrocarbons such as halogen-containing, acrylate-containing, allyl or vinyl ether-containing polyolefins, preferably in a proportion of 0.2 to less than 10% by weight, based on the total weight of the pressure-sensitive adhesive (layer).
  • the type and amount of the mixing components can be selected as required and the latter can also be higher than the preferred upper limits.
  • the adhesive (layer) does not contain some or even all of the additives mentioned in each case.
  • the present invention relates to a foamable pressure-sensitive adhesive which contains expandable, i.e. unexpanded, microballoons. It also relates to a foamed pressure-sensitive adhesive layer which contains microballoons which are at least partially expanded.
  • At least partially expanded microballoons is typically understood according to the invention to mean that the microballoons in their entirety are expanded at least to the extent that a reduction in density of the adhesive is effected to a technically meaningful extent compared to the same adhesive with the unexpanded microballoons. This means that the microballoons do not necessarily have to be completely expanded.
  • the individual microballoons, viewed individually, are preferably expanded to at least twice their maximum extent in the unexpanded state.
  • the term “at least partially expanded microballoons” can also mean that only some of the microballoons under consideration are (on) expanded.
  • the microballoons are fully expanded, i.e. the layer has been foamed in such a way that a minimum density of the layer is achieved for a given proportion of microballoons.
  • the foaming takes place in particular by the introduction and subsequent expansion of microballoons.
  • Microballoons are elastic and thus expandable microspheres in their basic state, which have a thermoplastic polymer shell. These spheres are filled with low-boiling liquids or liquefied gas.
  • low-boiling liquids or liquefied gas In particular, polyacrylonitrile, PVDC, PVC or polyacrylates are used as the shell material.
  • Hydrocarbons in particular are used as the low-boiling liquid lower alkanes, for example isobutane or isopentane, which are enclosed as a liquefied gas under pressure in the polymer shell.
  • the outer polymer shell softens.
  • the liquid propellant in the shell changes into its gaseous state.
  • the microballoons expand irreversibly and expand three-dimensionally. The expansion is finished when the internal and external pressures equalize. Since the polymer shell is retained, a closed-cell foam is achieved.
  • microballoons are commercially available, which differ essentially in terms of their size (6 to 45 ⁇ m diameter in the unexpanded state) and their starting temperatures (75 to 220 ° C.) required for expansion.
  • microballoons are also available as aqueous dispersions with a solid or microballoon content of approx. 40 to 45% by weight, and also as polymer-bound microballoons (masterbatches), for example in ethyl vinyl acetate with a microballoon concentration of approx. 65% by weight. Both the microballoon dispersions and the masterbatches, like the DU types, are conceivable for producing a foamed PSA of the invention.
  • a foamed pressure-sensitive adhesive layer according to the invention can also be produced with so-called pre-expanded microballoons.
  • pre-expanded microballoons for example, under the name Dualite® ® from Chase Corp. or with the type designation Expancel DE (Dry Expanded) commercially available from Nouryon.
  • At least 90% of all voids formed by microballoons in the foamed pressure-sensitive adhesive layer preferably have a maximum diameter of from 20 to 75 ⁇ m, more preferably from 25 to 65 ⁇ m.
  • Maximum diameter is understood to mean the maximum expansion of a microballoon in any spatial direction of the cryogenic fracture edge in the SEM.
  • the diameter is determined using a cryogenic edge in the scanning electron microscope (SEM) at 500-fold magnification. The diameter of each individual microballoon is determined graphically.
  • the microballoons can be added to the formulation as a batch, paste or as an uncut or blended powder. Furthermore, they can be suspended in a solvent.
  • the proportion of microballoons in the adhesive (layer) is typically from 0.3% by weight to 2.5% by weight, preferably between 0.5% by weight and 2.0% by weight and very particularly between 0.7% by weight and 1.7% by weight, based in each case on the overall composition of the adhesive (layer).
  • the information relates typically to unexpanded microballoons, and with regard to the foamed adhesive layer, typically to the unexpanded or pre-expanded microballoons used.
  • a pressure-sensitive adhesive comprising expandable hollow microspheres used according to the invention may additionally also contain non-expandable hollow microspheres.
  • the only decisive factor is that almost all caverns containing gas are closed by a permanently tight membrane, regardless of whether this membrane consists of an elastic and thermoplastically stretchable polymer mixture or, for example, of elastic and - in the range of temperatures possible in plastics processing - non-thermoplastic glass.
  • the density of the foamed PSA layer of the invention is at least 600 kg / m 3 and at most 920 kg / m 3 , preferably at least 650 kg / m 3 and at most 870 kg / m 3 , very preferably at least 700 kg / m 3 and a maximum of 820 kg / m 3 .
  • the typical application quantity range is particularly advantageous for microballoons with a maximum diameter of below 40 ⁇ m. In the case of microballoons with an expanded diameter of 40 ⁇ m, less than 2.0% is used.
  • the invention also relates to self-adhesive products, especially double-sided self-adhesive products, i.e. in particular double-sided adhesive tapes which contain at least one pressure-sensitive adhesive layer according to the invention. Adhesive transfer tapes are particularly advantageous.
  • the self-adhesive product can also contain a (permanent) intermediate carrier.
  • Self-adhesive tapes produced using at least one pressure-sensitive adhesive layer of the invention can accordingly in particular be designed as
  • Multilayer, double-sided self-adhesive tapes in which the layers each consist of the pressure-sensitive adhesive layers of the invention or a pressure-sensitive adhesive layer of the invention and a pressure-sensitive adhesive layer not according to the invention;
  • Adhesive tapes which are self-adhesive on both sides and have an intermediate carrier (a so-called permanent carrier) which is arranged either in a layer of adhesive or between two layers of adhesive.
  • Single-layer, double-sided self-adhesive products composed of a single pressure-sensitive adhesive layer according to the invention are preferred.
  • the intermediate carrier consists of only a single layer, in particular a polymer film. It is also preferred if the intermediate carrier contains at least one layer of a formulation which contains at least one type of vinyl aromatic block copolymer and at least one type of adhesive resin.
  • the double-sided products regardless of the type of intermediate carrier, can have a symmetrical or an asymmetrical product structure with regard to the type of pressure-sensitive adhesive layers, such as, for example, the composition and / or thickness of the pressure-sensitive adhesive layers.
  • Typical assembly forms of the pressure-sensitive adhesive layer of the invention are rolls of adhesive tape and adhesive strips, such as are obtained, for example, in the form of diecuts.
  • all layers essentially have the shape of a cuboid. More preferably, all layers are connected to one another over their entire surface.
  • the shape of diecuts differs from that of a cuboid. Shapes in which the angles between the width and length of the die cut are greater or less than 90 ° can be particularly advantageous; H. Have tapers. Diecuts can also be a structure of adhesive tape webs which also encircle areas free of adhesive tape. Diecuts can also have different types of other recesses.
  • adheresive tape encompasses all flat structures such as films or film sections extended in two dimensions, tapes with extended length and limited width, tape sections and the like, ultimately also diecuts or labels.
  • the adhesive tape thus has a longitudinal dimension and a width dimension.
  • the adhesive tape also has a thickness running perpendicular to both dimensions, the width dimension and the longitudinal dimension being able to be many times greater than the thickness.
  • the thickness is as equal as possible, preferably essentially the same, over the entire surface area of the adhesive tape determined by the length and width.
  • the adhesive tape is in web form.
  • a path is understood to mean an object whose length is many times greater than the width and the width is preferably designed to be exactly the same along the entire length.
  • the adhesive tape can be produced in the form of a roll, that is to say rolled up on itself in the form of an Archimedean spiral.
  • adhesive layers according to the invention in self-adhesive products are also conceivable, ie in particular adhesive tapes which can be removed from an adhesive bond by stretching, for example in the bond plane, essentially without leaving any residue or destruction, so-called strippable adhesive film strips or self-adhesive strips.
  • strippable adhesive film strips In order for the relevant known strippable adhesive film strips to be removed easily and without leaving any residue, they must have certain technical adhesive properties:
  • strippable adhesive tapes In order that strippable adhesive tapes can be removed again easily and without leaving any residue, they must have certain mechanical properties in addition to the adhesive properties described above.
  • the ratio of the tear force and the stripping force is particularly advantageously greater than two, preferably greater than three.
  • such strips also have good tear strength.
  • the stripping force is the force that has to be used to release an adhesive strip from an adhesive joint by pulling it in parallel in the direction of the bond plane.
  • This stripping force is made up of the force that is required to detach the adhesive tape from the adhesive substrates, as described above, and the force that has to be used to deform the adhesive tape. The force required to deform the adhesive tape depends on the thickness of the adhesive film strip.
  • the force required for detachment is independent of the thickness of the adhesive strip in the thickness range of the adhesive film strip considered (50 ⁇ m to 800 ⁇ m).
  • the tensile strength increases proportionally to the thickness of the adhesive strips. It follows from this that for self-adhesive tapes with a single-layer structure, as disclosed in DE 33 31 016 C2, the tensile strength below a certain thickness is smaller than that Pull-off force. Above a certain thickness, however, the ratio of pull-off force to stripping force is greater than two.
  • Foamed PSA layers according to the invention are used in self-adhesive products as described above. These self-adhesive products can be designed as an adhesive film, adhesive tape or adhesive die cut.
  • the self-adhesive products contain at least one foamed pressure-sensitive adhesive layer according to the invention.
  • This layer can have a layer thickness of 10 to 2000 ⁇ m. The thickness is preferably between 15 ⁇ m and 250 ⁇ m, more preferably between 25 ⁇ m and 150 ⁇ m, in particular it is at most 100 ⁇ m.
  • Example layer thicknesses are 30 pm, 50 pm, 75 pm, 100 pm, 125 pm, 150 pm, 200 pm and 250 pm. Layer thicknesses of 500 to 2000 ⁇ m, such as in particular 1000 to 1500 ⁇ m, are likewise preferred.
  • the thickness can be 750 or 1000 ⁇ m.
  • the self-adhesive products are typically designed to be adhesive on both sides. The advantages of the formulations according to the invention can be used particularly well in double-sided adhesive self-adhesive products when two components, and in particular in a mobile device, are to be glued to one another.
  • the inventive concept also encompasses structures with an intermediate carrier (also called permanent carrier) within the self-adhesive product, in particular in the middle of the single pressure-sensitive adhesive layer.
  • the intermediate carrier is stretchable, the stretchability of the intermediate carrier having to be sufficient for some applications in order to ensure that the adhesive strip is detached by stretching.
  • Very stretchable foils can serve as intermediate carriers.
  • a maximum stretchability of the film in at least one direction, preferably in both directions, of at least 250%, preferably of at least 400% (ISO 527-3) is advantageous.
  • Examples of advantageously replaceable expandable intermediate carriers are designs from WO 2011/124782 A1, DE 10 2012 223 670 A1, WO 2009/114683 A1, WO 2010/077541 A1, WO 2010/078396 A1.
  • stretchable intermediate carrier film film-forming or extrudable polymers are used, which can also be mono-axially or biaxially oriented.
  • polyolefins are used.
  • Preferred polyolefins are made from ethylene, propylene, butylene and / or hexylene, the pure in each case
  • Monomers can be polymerized or mixtures of the monomers mentioned can be copolymerized.
  • the polymerization process and the selection of the monomers allow the physical and mechanical properties of the polymer film to be controlled, such as the softening temperature and / or the tear strength.
  • Polyurethanes can preferably be used as starting materials for stretchable intermediate carrier layers.
  • Polyurethanes are chemically and / or physically crosslinked polycondensates that are typically built up from polyols and isocyanates.
  • expandable materials are available which can be used advantageously for the purposes of this invention.
  • Raw materials which are available to the formulator for this purpose are mentioned, for example, in EP 0 894 841 B1 and EP 1 308 492 B1. The person skilled in the art is familiar with further raw materials from which intermediate carrier layers according to the invention can be built up.
  • rubber-based materials in intermediate carrier layers in order to achieve extensibility.
  • natural rubber can basically be made from all available qualities such as crepe, RSS, ADS, TSR or CV types, depending on the required level of purity and viscosity, and synthetic rubber or the synthetic rubbers from the group of randomly copolymerized styrene-butadiene rubbers (SBR), butadiene rubbers (BR), synthetic polyisoprenes (IR), butyl rubbers (IIR), halogenated butyl rubbers (XI IR) , the acrylate rubbers (ACM), the ethylene vinyl acetate copolymers (EVA) and the polyurethanes and / or their blends can be selected.
  • SBR randomly copolymerized styrene-butadiene rubbers
  • BR butadiene rubbers
  • IR butyl rubbers
  • XI IR halogenated butyl rubbers
  • ACM acrylate rubbers
  • EVA ethylene vinyl
  • Block copolymers are particularly advantageously replaceable as materials for stretchable intermediate carrier layers. Individual polymer blocks are covalently linked to one another. The block linkage can be in a linear form, but also in a star-shaped or graft copolymer variant.
  • An example of an advantageously replaceable block copolymer is a linear triblock copolymer whose two terminal blocks have a softening temperature of at least 40.degree. C., preferably at least 70.degree. C., and whose central block has a softening temperature of at most 0.degree has a maximum of -30 ° C. Higher block copolymers, such as tetra block copolymers, can also be replaced.
  • the block copolymer contains at least two polymer blocks of the same or different types which each have a softening temperature of at least 40 ° C, preferably at least 70 ° C and which have a softening temperature of at most 0 ° C, preferably at most - 30 ° C are separated from each other in the polymer chain.
  • polymer blocks are polyethers, such as, for example, polyethylene glycol, polypropylene glycol or polytetrahydrofuran, polydienes, such as, for example, polybutadiene or polyisoprene, hydrogenated polydienes, such as, for example, polyethylene butylene or polyethylene propylene, polyesters, such as, for example, polyethylene terephthalate, polybutanediol vinyl adipate, polyhexanediol adipate Monomers, such as, for example, polystyrene or poly- [a] -methylstyrene, polyalkyl vinyl ethers, polyvinyl acetate, polymer blocks [a], [ß] -unsaturated esters such as, in particular, acrylates or methacrylates.
  • polyethers such as, for example, polyethylene glycol, polypropylene glycol or polytetrahydrofuran
  • polydienes such as, for example, polybutadiene or poly
  • an intermediate carrier material it may also be advisable here to add additives and other components that improve the film-forming properties, reduce the tendency to form crystalline segments and / or specifically improve or possibly worsen the mechanical properties.
  • Foams in web form are also suitable.
  • the intermediate carriers can be designed in multiple layers.
  • the intermediate carriers can have cover layers, for example barrier layers, which prevent the penetration of components from the adhesive into the intermediate carrier or vice versa. These cover layers can also have barrier properties in order to prevent water vapor and / or oxygen from diffusing through.
  • the intermediate carriers can be pretreated using known measures such as corona, plasma or flames. The use of a primer is also possible. Ideally, however, pre-treatment can be dispensed with.
  • the inventive concept also includes structures with an intermediate carrier with a high modulus of elasticity and low extensibility within the self-adhesive product, in particular in the middle of the single pressure-sensitive adhesive layer, the modulus of elasticity of the intermediate carrier advantageously being at least 750 MPa, preferably at least 1 GPa (ISO 527-3) and the maximum extensibility (according to ISO 527-3) is in particular a maximum of 200%.
  • Such structures are particularly easy to replace in stamping processes and make them easier to handle in the application process.
  • Permanent carriers of this type are also advantageous if the self-adhesive product is to be detached again by peeling.
  • film-forming or extrudable polymers are used which, in particular, can additionally be mono-axially or biaxially oriented.
  • Polyester films and particularly preferably films based on polyethylene terephthalate (PET) are particularly suitable as film material for the at least one layer of a film for this embodiment.
  • Polyester films are preferably biaxially stretched.
  • Films made from polyolefins, in particular from polybutene, cyclo-olefin copolymer, polymethylpentene, polypropylene or polyethylene, for example made from monoaxially stretched polypropylene, biaxially stretched polypropylene or biaxially stretched polyethylene, are also conceivable. This list is intended to show examples; further systems are known to the person skilled in the art which correspond to the concept of the present invention.
  • an intermediate carrier material it may also be advisable here to add additives and other components that improve the film-forming properties, reduce the tendency to form crystalline segments and / or specifically improve or possibly worsen the mechanical properties.
  • the intermediate carriers can be designed in multiple layers. Furthermore, the intermediate carriers can have cover layers, for example barrier layers, which prevent the penetration of components from the adhesive into the intermediate carrier or vice versa. These cover layers can also have barrier properties in order to prevent water vapor and / or oxygen from diffusing through.
  • the intermediate carriers can be pretreated using known measures such as corona, plasma or flames.
  • the use of a primer is also possible. Ideally, however, pre-treatment can be dispensed with.
  • the thickness of the intermediate carrier layer is typically in the range from 2 ⁇ m to 200 ⁇ m, preferably between 5 and 100 ⁇ m and in particular between 10 and 80 ⁇ m.
  • the self-adhesive product such as, in particular, adhesive tape
  • a liner that is to say a temporary carrier that has an anti-adhesive coating on one or both sides.
  • a liner (release paper, release film) is not part of an adhesive tape but only an aid for its production, storage or for further processing by punching. In addition, unlike an adhesive tape backing, a liner is not firmly connected to an adhesive layer.
  • the formulations i.e. pressure-sensitive adhesives, and the coatings or self-adhesive products produced therefrom can be produced using organic solvents or without solvents.
  • the substrate is preferably a planar element, in particular a carrier material, a film, a (release) liner, a transfer material and / or a cover material.
  • Substrates can also be the surfaces of the production line in the manufacturing process.
  • a pressure-sensitive adhesive is processed into at least one pressure-sensitive adhesive layer with a thickness of greater than or equal to 15 ⁇ m or even greater than or equal to 10 ⁇ m, and the flatly applied pressure-sensitive adhesive layer is optionally dried or the solvents are removed.
  • a hotmelt adhesive is processed solvent-free.
  • the coating processes used for the planar elements used according to the invention include knife-edge processes, knife-edge knife processes, roller-bar nozzle processes, extrusion nozzle processes, pouring nozzles and pouring processes.
  • Application methods such as roller application methods, printing methods, screen printing methods, anilox roller methods, inkjet methods and spraying methods are also according to the invention. Hotmelt processes (extrusion, nozzle) are preferred.
  • the resulting combination of planar element and pressure-sensitive adhesive is cut to length goods comprising tapes and / or diecuts are punched out, and the tapes are optionally rolled up to form a banderole.
  • the invention also extends to adhesive composites obtained by using self-adhesive products which contain at least one pressure-sensitive adhesive layer according to the invention. That is to say, the invention relates to a composite of an adhesive tape according to the invention and two substrates, such as in particular components of a mobile device, which are connected with the adhesive tape.
  • the invention particularly preferably relates to the bonding of mobile devices, since the adhesive tape used according to the invention is particularly useful here because of the unexpectedly good properties (very high shock resistance).
  • Some portable devices, ie mobile devices, are listed below, without wishing to restrict the subject matter of the invention unnecessarily by the specifically named representatives in this list. • Cameras, digital cameras, photography accessories (such as light meters, flash units, bezels, photo housings, lenses, etc.), film cameras, video cameras
  • Monitors displays, screens, touch-sensitive screens (touch screens, “touchscreen devices”), projectors
  • Radios also small and pocket radios
  • walkmen also small and pocket radios
  • disemen music players for e.g. CD, DVD, Blu-ray, cassettes, USB, MP3, headphones
  • the determination of the bond strength is carried out as follows.
  • a polished steel plate with a thickness of 2 mm is used as a defined primer.
  • the bondable surface element to be examined (which is equipped on the back with a 36 ⁇ m etched PET film as a support film) is cut to a width of 20 mm and a length of about 25 cm, provided with a handling section and immediately afterwards with a steel roller of 4 kg at a feed rate of 10 m / min onto the chosen primer.
  • the measured value (in N / cm) is the mean value from three individual measurements.
  • the adhesive tape to be examined (50 ⁇ m transfer tape) is stuck to one of the sides of the adhesive on a 50 ⁇ m thick aluminum foil.
  • the adhesive tape prepared in this way is cut to a size of 10 mm * 50 mm.
  • the sample is reinforced flush with a sturdy adhesive strip that serves as a support for the displacement sensor.
  • the sample is then suspended by means of the steel plate in such a way that the longer protruding end of the adhesive tape points vertically downwards.
  • the lower end of the sample to be measured is loaded with a weight of 50 g.
  • the steel test plate with the bonded sample is heated to the final temperature of 200 ° C starting at 25 ° C at a rate of 9 K / min.
  • the slipping path of the sample is observed by means of a displacement sensor as a function of temperature and time.
  • the maximum slip distance is set at 1000 pm (1 mm); if it is exceeded, the test is aborted and the failure temperature is noted.
  • Test climate room temperature 23 +/- 3 ° C, relative humidity 50 +/- 5%. The result is the mean value from two individual measurements and is given in ° C.
  • Test III dielectric strength; z-plane (DuPont test)
  • a square, frame-shaped sample is cut out of the adhesive tape to be examined (external dimensions 33 mm x 33 mm; web width 2.0 mm; internal dimensions (window cutout) 29 mm x 29 mm).
  • This sample is glued to a polycarbonate (PC) frame (external dimensions 45 mm ⁇ 45 mm; web width 10 mm; internal dimensions (window cutout) 25 mm ⁇ 25 mm; thickness 3 mm).
  • a PC window measuring 35 mm x 35 mm is glued to the other side of the double-sided adhesive tape.
  • the PC frame, adhesive tape frame and PC window are glued in such a way that the geometric centers and the diagonals are each superimposed (corner-to-corner).
  • the bond area is 248 mm 2 .
  • the bond is pressed with 248 N for 5 s and stored conditioned for 24 hours at 23 ° C / 50% relative humidity.
  • the adhesive composite of PC frame, adhesive tape and PC window is clamped with the protruding edges of the PC frame in a sample holder in such a way that the composite is aligned horizontally.
  • the PC frame lies flat on the protruding edges of the sample holder, so that the PC window is freely floating (held by the adhesive tape pattern) below the PC frame.
  • the specimen holder is then placed centrically in the intended receptacle of the "DuPont Impact Tester".
  • the 150 g impact head is used in such a way that the circular impact geometry with a diameter of 24 mm rests centrally and flush on the surface of the PC window that is freely accessible from above.
  • the height of the falling weight is increased in 5 cm steps until the impact energy introduced destroys the sample due to the impact load and the PC window detaches from the PC frame.
  • the glass transition temperature of polymer blocks in block copolymers is determined by means of dynamic scanning calorimetry (DSC). For this purpose, approx. 5 mg of the untreated block copolymer samples are weighed into a small aluminum crucible (volume 25 ⁇ l) and closed with a perforated lid. A DSC 204 F1 from Netzsch is used for the measurement and inertization is carried out under nitrogen. The sample is first cooled to -150 ° C, heated to +150 ° C at a heating rate of 10 K / min and then cooled again to -150 ° C. The subsequent second heating curve is run again at 10 K / min and the change in heat capacity is recorded. Glass transitions are recognized as steps in the thermogram.
  • DSC dynamic scanning calorimetry
  • the glass transition temperature is evaluated as follows (see Figure 3). A tangent is applied to the baseline of the thermogram before 1 and after 2 of the level. In the area of the step, a regression line 3 is laid parallel to the ordinate so that it intersects the two tangents in such a way that two surfaces 4 and 5 (between the one tangent, the regression line and the measurement curve) have the same content. The intersection of the regression line positioned in this way with the measurement curve gives the glass transition temperature. Test V - Molecular Weight (GPC)
  • GPC can be used as a metrological method to determine the molar mass of individual polymer modes in mixtures of different polymers.
  • the molar mass distributions are typically sufficiently narrow so that polymer modes which can be assigned to T riblock copolymers, diblock copolymers or multiblock copolymers occur sufficiently resolved from one another in the eligram.
  • the peak molar mass for the individual polymer modes can then be read off from the elograms.
  • the (adhesive) resin softening temperature also known as the (adhesive) resin softening point, is carried out according to the relevant methodology known as Ring & Ball and standardized according to ASTM E28.
  • Test VII-DACP is carried out according to the relevant methodology known as Ring & Ball and standardized according to ASTM E28.
  • test substance the adhesive resin sample to be examined
  • xylene isomer mixture, CAS [1330-20-7],> 98.5%, Sigma-Aldrich # 320579 or comparable
  • the test substance is dissolved at 130 ° C and then cooled to 80 ° C. Any xylene that has escaped is topped up with additional xylene so that 5.0 g of xylene are again available.
  • diacetone alcohol 4-hydroxy-4-methyl-2-pentanone, CAS [123-42-2], 99%, Aldrich # H41544 or comparable
  • the solution is heated to 100 ° C.
  • the sample glass with the resin solution is then placed in a cloud point measuring device Chemotronic Cool from Novomatics and heated there to 110 ° C. It is cooled at a cooling rate of 1.0 K / min.
  • the cloud point is detected optically.
  • the temperature at which the turbidity of the solution is 70% is recorded. The result is given in ° C.
  • the lower the DACP value the higher the polarity of the test substance.
  • a shear stress sweep is carried out in rotation in a shear stress-controlled DSR 200 N rheometer from Rheometrics Scientific.
  • a cone / plate measuring system with a diameter of 25 mm (cone angle 0.1002 rad) is used, the measuring head has air bearings and is suitable for normal force measurements.
  • the gap is 0.053 mm and the measuring temperature is 25 ° C.
  • the frequency is varied from 0.002 Hz to 200 Hz and the melt viscosity is registered at 1 Hz.
  • the density that is to say absolute density, of an adhesive or adhesive layer is determined by forming the quotient of the amount of material applied and the thickness of the adhesive layer applied to a carrier or liner.
  • the application of mass can be determined by determining the mass of a section defined in terms of its length and width of such an adhesive mass (layer) applied to a carrier or liner, minus the (known or separately ascertainable) mass of a section of the same dimensions of the carrier or liner used. Liners.
  • the thickness of an adhesive can be determined by determining the thickness of a section defined in terms of its length and width of such an adhesive layer applied to a carrier or liner, minus the (known or separately ascertainable) thickness of a section of the same dimensions of the T used rägers or liners.
  • the thickness of the adhesive (layer) can be determined using commercially available thickness measuring devices (button test devices) with an accuracy of less than 1 ⁇ m.
  • the precision thickness measuring device model 2000 F from Wolf Messtechnik GmbH is used, which has a circular probe with a diameter of 10 mm (flat).
  • the measuring force is 4 N.
  • the value is read 1 s after the load. If fluctuations in thickness are found, the mean value of measurements is given at at least three representative points, that is to say in particular not measured at kinks, folds, specks and the like.
  • the pressure-sensitive adhesive (layer) of the invention is described below in a preferred embodiment using a number of examples, without thereby wishing to restrict the invention in any way.
  • the constituents of the PSAs were dissolved at 40% in special boiling point spirit / toluene / acetone, mixed with the microballoons suspended in gasoline, and spread with a spreader bar in the desired layer thickness onto a PET film equipped with a separating silicone.
  • the solvent was then evaporated off at 100 ° C. for 15 min and the mass layer was dried in this way. This is possible in the examples given because microballoons are used here whose expansion temperature is above 100 ° C. When using other microballoons, the person skilled in the art selects appropriate manufacturing temperatures without departing from the scope of the present invention.
  • the adhesive layer was covered with a second layer of PET liner as defined above, free of any air inclusions, and foamed for 30 s at 170 ° C. between the two liners in a circulating drying cabinet.
  • Table 2 shows the raw materials used.
  • Tables 3a to 3f show the formulations of the examples and comparative examples (percentages of the compositions are% by weight) and their characteristics.
  • Table 3b further recipes and their characteristics.
  • Table 3c further recipes and their characteristics.
  • Table 3d further recipes and their characteristics.
  • Table 3e further recipes and their characteristics.
  • Table 3f further recipes and their characteristics.
  • a comparison of Examples C1, E2, E3 and E4 shows in particular the positive influence of the proportion of grade K1 of a rosin oligomer with a softening temperature (Ring & Ball, Test VI) of at least 90 ° C on the shock resistance and the bond strength, with comparable thermal shear strength.
  • a comparison of Examples C5 and E6 to E9, in which a different type of adhesive resin K1 is used likewise shows, in particular, the positive influence of the proportion of type K1 on the shock resistance and the bond strength, with comparable thermal shear strength. It is particularly interesting here that the shock resistance and the adhesive strength pass through a maximum depending on the proportion of type K1.
  • C10 and E11 show the relationships shown using a different elastomer or adhesive resin K1.
  • C1 and E12 show the relationships shown using a modified elastomer composition.
  • Example C17 shows in particular that too little elastomer has a negative effect on shock resistance.
  • Table 3f shows that the selection of the amount of microballoons used is also essential for achieving the desired improvement in performance, in particular shock resistance.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Adhesive Tapes (AREA)

Abstract

L'invention concerne une couche de masse adhésive expansée comprenant a) de 41,7 à 62,0 % en poids d'un composant élastomère, b) de 37,7 à 58,0 % en poids d'un composant de résine adhésive, c) de 0 à 15 % en poids d'un composant de résine souple, d) de 0 à 18 % en poids d'autres additifs, et e) des microballons ayant une proportion de préférence de 0,3 à 2,5 % en poids, de préférence de 0,5 à 2,0 % en poids et de manière particulièrement préférée de 0,7 à 1,7 % en poids, les microballons étant au moins partiellement expansés, le composant élastomère (a) consistant en au moins 90 % en poids d'un copolymère séquencé polydine composé aromatique polyvinylique, le composant de résine adhésive (b) contient jusqu'à 4 à 100 % en poids d'au moins un type K1 si un oligomère de colophane ayant une température de ramollissement (bille et anneau, Test VI) d'au moins 90 °C, et la densité (texte IX) de la couche de masse adhésive expansée étant d'au moins 600 kg/m ³ et d'au plus 920 kg/m ³.
EP20800890.4A 2019-11-04 2020-11-03 Couche de masse adhésive expansée et ruban adhésif comprenant la couche de masse adhésive expansée Pending EP4055110A1 (fr)

Applications Claiming Priority (2)

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DE102019216938.4A DE102019216938A1 (de) 2019-11-04 2019-11-04 Geschäumte Haftklebemasseschicht und Klebeband enthaltend die geschäumte Haftklebemasseschicht
PCT/EP2020/080777 WO2021089523A1 (fr) 2019-11-04 2020-11-03 Couche de masse adhésive expansée et ruban adhésif comprenant la couche de masse adhésive expansée

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US (1) US20220380641A1 (fr)
EP (1) EP4055110A1 (fr)
KR (1) KR20220092587A (fr)
CN (1) CN114641547A (fr)
DE (1) DE102019216938A1 (fr)
WO (1) WO2021089523A1 (fr)

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DE102019216942A1 (de) * 2019-11-04 2021-05-06 Tesa Se Haftklebemassen,diese enthaltende Selbstklebeprodukte und Verbunde
DE102021206799A1 (de) * 2021-06-30 2023-01-05 Tesa Se Stanzbares Reaktivklebeband
DE102022107748A1 (de) 2022-03-31 2023-10-05 Tesa Se Klebeband zur Verklebung auf Lacken
DE102023109899A1 (de) * 2023-04-19 2024-10-24 Tesa Se Selbstklebeband mit MOPP-Träger

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DE3331016A1 (de) 1983-04-06 1984-10-11 Beiersdorf Ag, 2000 Hamburg Klebfolie fuer wiederloesbare klebbindungen
DE19733014A1 (de) 1997-07-31 1999-02-04 Beiersdorf Ag Selbstklebeband
DE10153677A1 (de) 2001-10-31 2003-05-15 Tesa Ag Doppelseitiges Klebeband
DE102008004388A1 (de) * 2008-01-14 2009-07-16 Tesa Ag Geschäumte, insbesondere druckempfindliche Klebemasse, Verfahren zur Herstellung sowie die Verwendung derselben
US8673419B2 (en) 2008-03-14 2014-03-18 3M Innovative Properties Company Stretch releasable adhesive tape
DE102008056980A1 (de) * 2008-11-12 2010-05-20 Tesa Se Strahlenchemisch vernetzbare, geschäumte Selbstklebemasse basierend auf Vinylaromatenblockcopolymeren
CN102325850B (zh) 2008-12-31 2014-03-12 3M创新有限公司 可拉伸剥离的粘合带
US8703977B2 (en) 2009-01-02 2014-04-22 Emory University Compounds, intermediates, and methods of preparing the same
FR2957905B1 (fr) 2010-03-29 2012-04-06 Otor Sa Procede et dispositif de transfert de decoupes pour boites d'emballage
DE102012223670A1 (de) 2012-12-19 2014-06-26 Tesa Se Wiederablösbarer Haftklebestreifen
DE102013206624A1 (de) * 2013-04-15 2014-10-16 Tesa Se Haftklebemasse und Verwendung derselben in einem Haftklebstreifen
JP6199734B2 (ja) 2013-12-26 2017-09-20 住友ゴム工業株式会社 タイヤ用ゴム組成物及び空気入りタイヤ
DE102016202018A1 (de) * 2016-02-10 2017-08-10 Tesa Se Haftklebemasse, diese enthaltende Selbstklebeprodukte und Verbunde
DE102016209707A1 (de) * 2016-06-02 2017-12-07 Tesa Se Haftklebestreifen
EP3333235B1 (fr) * 2016-12-09 2023-06-07 tesa SE Bande adhésive

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US20220380641A1 (en) 2022-12-01
KR20220092587A (ko) 2022-07-01
WO2021089523A1 (fr) 2021-05-14
DE102019216938A1 (de) 2021-05-06
CN114641547A (zh) 2022-06-17

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