WO2022268837A1 - Biologisch abbaubare haftklebemasse - Google Patents

Biologisch abbaubare haftklebemasse Download PDF

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Publication number
WO2022268837A1
WO2022268837A1 PCT/EP2022/066925 EP2022066925W WO2022268837A1 WO 2022268837 A1 WO2022268837 A1 WO 2022268837A1 EP 2022066925 W EP2022066925 W EP 2022066925W WO 2022268837 A1 WO2022268837 A1 WO 2022268837A1
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WO
WIPO (PCT)
Prior art keywords
pressure
sensitive adhesive
acid
polyhydroxyalkanoate
adhesive
Prior art date
Application number
PCT/EP2022/066925
Other languages
German (de)
English (en)
French (fr)
Inventor
Philipp WEGENER
Ernesto Rafael OSORIO BLANCO
Sara Schröder
Original Assignee
Tesa Se
Beiersdorf Ag
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, Beiersdorf Ag filed Critical Tesa Se
Priority to EP22735868.6A priority Critical patent/EP4359463A1/de
Priority to AU2022299275A priority patent/AU2022299275A1/en
Publication of WO2022268837A1 publication Critical patent/WO2022268837A1/de

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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
    • C09J167/00—Adhesives based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Adhesives based on derivatives of such polymers
    • C09J167/04—Polyesters derived from hydroxycarboxylic acids, e.g. lactones
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00—Bandages or dressings; Absorbent pads
    • A61F13/02—Adhesive bandages or dressings
    • A61F13/0246—Adhesive bandages or dressings characterised by the skin-adhering layer
    • A61F13/0253—Adhesive bandages or dressings characterised by the skin-adhering layer characterized by the adhesive material
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/06—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from hydroxycarboxylic acids
    • 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]
    • 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
    • C09J2467/00—Presence of polyester

Definitions

  • the invention relates to the technical field of pressure-sensitive adhesives, such as are used in many areas of technology for the temporary or permanent bonding of a wide variety of substrates and also in medicine for providing dressings for bonding to the skin. More specifically, the invention proposes a pressure-sensitive adhesive based on a polyhydroxyalkanoate, which has significantly improved biodegradability compared to conventional pressure-sensitive adhesives.
  • biodegradable plastics or materials based on biodegradable polymers receive the greatest attention.
  • Biodegradable polymers is a term for natural, bioidentical and synthetic polymers which, in contrast to conventional plastics, are broken down by a large number of microorganisms in a biologically active environment (compost, sludge, soil, waste water); this does not necessarily happen under normal household conditions (composting in the garden).
  • a definition of biodegradability can be found in the European standard DIN EN 13432 (biological degradation of packaging) and the international standard ISO 14855-1 (aerobic biodegradability of plastics).
  • Disintegration refers to the physical decomposition into very small fragments.
  • the material to be tested is subjected to an aerobic degradation test, and a degree of degradation of at least 90% compared to a suitable reference substance must be achieved within a maximum of six months.
  • the degree of degradation is determined by the measured development of carbon dioxide.
  • the comminuted sample is stored with vermiculite or well-performing aerated compost as inoculum in an air-fed vessel at 58 ⁇ 2°C and CO 2 evolution continuously recorded. Due to the complexity of the equipment, there are a number of testing institutes that have specialized in testing and then issue a corresponding certificate.
  • the degradation rate D is found according to equation (2) below as:
  • ThC0 2 the theoretical amount of carbon dioxide that can be formed by the test substance, in grams per vessel.
  • DIN EN 13432 also includes a test to determine the quality of the compost resulting from degradation. This must not have any negative effects on plant growth. As a rule, biodegradable components also have a high rate of disintegration, whereas the disintegration of a material does not necessarily indicate biodegradability.
  • MVTR water vapor permeability
  • heteroatoms in the main carbon chain is generally regarded as a structural condition for biodegradability. This is due to the higher polarity of the bond and the existing lone pairs of electrons
  • Heteroatoms have higher reactivity than CC bonds, often in better Accessibility to microbial degradation results, for example through hydrolysis.
  • Advantageous polymers as a basis for biodegradable adhesives are therefore those that have functional groups such as ester, amide, imine or enamine groups, which can then act as points of attack for biological degradation.
  • the backing paper consists of silicone oil-coated glassine paper; the surface material layer includes the following composition:
  • nucleating agent 0.3 to 1 part by weight of nucleating agent
  • the adhesive layer comprises the following composition:
  • a first and general subject of the invention is a pressure-sensitive adhesive which comprises at least one polyhydroxyalkanoate and which is characterized in that the polyhydroxyalkanoate
  • - comprises from 20 to 75% by weight of structural units deriving from 3-hydroxybutyric acid (3-HB); and at least one further structural unit which is based on a hydroxyalkanoic acid selected from the group consisting of 4-hydroxybutyric acid (4-HB), 3-hydroxyvaleric acid (3-HV), 4-hydroxyvaleric acid (4-HV), 3-hydroxyhexanoic acid (3- HX) and/or 4-hydroxyhexanoic acid (4-HX).
  • PSAs of this type have proven to be high-performing and reliably biodegradable.
  • a pressure-sensitive adhesive can be regarded as an extremely highly viscous liquid with an elastic portion, which consequently has characteristic viscoelastic properties that lead to the permanent inherent tack and pressure-sensitive adhesiveness described above. It is assumed that, in the case of pressure-sensitive adhesives, mechanical deformation leads both to viscous flow processes and to the build-up of elastic restoring forces. Of the The proportionate viscous flow serves to achieve adhesion, while the proportionate elastic restoring forces are necessary in particular to achieve cohesion.
  • the relationships between rheology and pressure-sensitive tack are known in the prior art and are described, for example, in "Satas, Handbook of Pressure Sensitive Adhesives Technology", Third Edition, (1999), pages 153 to 203.
  • Polyhydroxyalkanoates also known as PHAs for short, are polyesters that can formally be traced back to a monomer base of one or more hydroxyalkanoic acids. They accordingly have a structure of the formula H-[-0-RC(0)-] n -0H, where R is a branched or unbranched and functionalized or unfunctionalized alkylene radical.
  • PHAs are generally not synthesized by way of a polymerization of hydroxyalkanoic acids, but biologically produced by bacterial cultures. The composition of the PHAs is controlled by the biological material made available to the bacteria and in particular by the selection of the bacteria.
  • the hydroxyalkanoic acids on which the polyhydroxyalkanoate of the PSA of the invention is formally based are preferably hydroxylated in the 3- or 4-position.
  • the polyhydroxyalkanoate thus has a side functionalization of alkyl groups on its main chain in part.
  • the polyhydroxyalkanoate comprises 20 to 75% by weight of structural units which can be traced back to 3-hydroxybutyric acid.
  • the PHA thus has methyl groups protruding from the main chain on these structural units.
  • the polyhydroxyalkanoate of the pressure-sensitive adhesive of the invention also preferably has a glass transition temperature of less than 0.degree. This property has an advantageous effect on what is known as the flowability of the pressure-sensitive adhesive and ultimately also on its adhesive strength.
  • the polyhydroxyalkanoate of the pressure-sensitive adhesive of the invention can, in principle, comprise further structural units which are attributable to hydroxyalkanoic acids in addition to those previously mentioned. However, these structural units are preferably present in minor proportions. Examples of such further structural units are 3-hydroxyheptanoic acid, 3-hydroxyoctanoic acid, 3-hydroxynonanoic acid, 3-hydroxydecanoic acid, 3-hydroxyundecanoic acid, 3-hydroxydodecanoic acid, 4-hydroxyhexanoic acid, 4-hydroxyheptanoic acid, 4-hydroxyoctanoic acid, 4-hydroxynonanoic acid, 4-hydroxydecanoic acid, 4-hydroxyundecanoic acid and 4-hydroxydodecanoic acid.
  • the PHA comprises excluding structural units based on 3-hydroxybutyric acid (3-HB), 4-hydroxybutyric acid (4-HB), 3-hydroxyvaleric acid (3-HV), 4-hydroxyvaleric acid (4-HV), 3-
  • the crosslinking is initiated by free radicals.
  • the polyhydroxyalkanoate of the PSA of the invention is preferably free-radically crosslinked
  • Crosslinking is particularly preferably initiated by a compound selected from the group consisting of dibenzoyl peroxide, cumene hydroperoxide, cyclohexanone peroxide, di-t-butyl peroxide, cyclohexylsulfonyl acetyl peroxide, dicumyl peroxide (DCP) and 4-benzoylphenyl acrylate.
  • a compound selected from the group consisting of dibenzoyl peroxide, cumene hydroperoxide, cyclohexanone peroxide, di-t-butyl peroxide, cyclohexylsulfonyl acetyl peroxide, dicumyl peroxide (DCP) and 4-benzoylphenyl acrylate.
  • the pressure-sensitive adhesive or the composition to be crosslinked to produce the pressure-sensitive adhesive preferably contains one or more free-radical initiators in a total amount of from 0.1 to 10% by weight, more preferably from 0.5 to 7% by weight, in particular from 1 to 5% % by weight, based in each case on the total weight of PSA or of the composition.
  • the polyhydroxyalkanoate is chemically crosslinked.
  • the crosslinking is effected by means of a chemical crosslinker.
  • This is a linear or branched compound with at least two reactive centers, ie at least two functionalities in the molecule, which can react with suitable functional groups of the polyhydroxyalkanoate to form chemical bonds.
  • Preferred crosslinkers are compounds containing one or more epoxide groups, isocyanate groups, carbodiimide groups, C-C double bonds, aldehyde groups, OH groups, carboxylic acid groups and/or amino groups.
  • crosslinkers are mixed into the composition containing the polyhydroxyalkanoate to be crosslinked; then the crosslinking reaction is initiated.
  • the initiation usually takes place through temperature input, but can also start at room temperature.
  • it may be necessary to use a crosslinking catalyst or a substance with an accelerating effect.
  • the chemical crosslinking takes place via the terminal functional groups of the polymer chains of the PHA, ie usually via terminal COOH and/or OH groups.
  • the polyhydroxyalkanoate it is possible for the polyhydroxyalkanoate to have functional groups suitable for a crosslinking reaction.
  • the PHA can be used in the non-networked io 0.1 to 25% by weight, more preferably 2 to 15% by weight, in particular 5 to 12% by weight, of structural units containing functional groups suitable for crosslinking.
  • the functional groups suitable for a crosslinking reaction can also be contained in the side functionalizations of the structural units.
  • the functional groups of the structural units of the PHA are preferably selected from the group consisting of C-C double bonds, hydroxy groups, carboxy groups and amino groups; most preferably they are terminal hydroxy and/or carboxy groups of the PHA polymer chains.
  • radical initiator e.g. 2,2'-azobis(2 -methylbutyronitrile)
  • Crosslinking can be carried out directly with this composition, but it is also possible to add 5 to 10% by weight, based on the PHA to be crosslinked, of monoethylenically unsaturated compounds as reactive diluents or co-substrates, for example (meth)acrylic esters , cyclic ketene acetals or itaconates.
  • the crosslinking reaction is carried out under a nitrogen atmosphere and is started either by UV radiation or by heating the reaction mixture to 80.degree. The mixture is stirred for 5 hours and the crosslinked composition formed is purified by precipitation or dialysis or used without further purification.
  • PHAs that are functionalized with carboxyl and/or hydroxyl groups and have a weight-average molecular weight M w of ⁇ 50,000 g/mol, preferably from 10,000 to 30,000 g/mol, can be crosslinked with a diisocyanate (NCO), for example with hexamethylene diisocyanate , isophorone diisocyanate and/or methylene diphenyl isocyanate.
  • NCO diisocyanate
  • the amount of diisocyanate to be used depends on the amount of carboxyl and hydroxyl groups in the PHA (OH number). An NCO:OH ratio of approx. 1 is aimed for.
  • the network obtained can be converted to the desired final crosslinking by adding typical COOH crosslinking agents, for example difunctional or multifunctional epoxy crosslinking agents such as tetraglycidyl-m-xylenediamine degree of networking are brought.
  • typical COOH crosslinking agents for example difunctional or multifunctional epoxy crosslinking agents such as tetraglycidyl-m-xylenediamine degree of networking are brought.
  • the degree of crosslinking is preferably 0.5 to 1% and is based on the carboxy groups.
  • crosslinking preferably takes place with a polyisocyanate, for example with trimerized hexamethylene diisocyanate.
  • a polyisocyanate for example with trimerized hexamethylene diisocyanate.
  • an NCO:OH ratio of 0.6 to 1 is aimed for.
  • the polyhydroxyalkanoate of the pressure-sensitive adhesive of the invention can also be crosslinked by physical methods, for example by forming blend systems with one or more substances selected from the group consisting of polylactic acid, cellulose, starch, sorbitol, mannose and polyglycerol.
  • the pressure-sensitive adhesive of the invention can have further components which are preferably likewise biodegradable.
  • the PSA of the invention preferably comprises one or more components selected from the group consisting of UV stabilizers, antioxidants, hydrophilizing agents, tackifiers, fillers, pigments, dyes, flame retardants, foaming agents, antistatic agents, plasticizers, surfactants, breathability improvers and sugar esters.
  • the PSA of the invention comprises one or more tackifiers and/or plasticizers.
  • the PSA of the invention comprises antibacterial (antiseptic) and/or skin care substances.
  • miscible plasticizers are aliphatic and aromatic mineral oils, polyethylene and polypropylene glycol, di- or polyesters of phthalic acid, citric acid, trimellitic acid or adipic acid, liquid rubbers (e.g. low molecular weight nitrile or polyisoprene rubbers), liquid polymers of butene and/or isobutene , acrylic acid esters, polyvinyl ether, liquid and soft resins based on the raw materials of adhesive resins, wool wax and other waxes or liquid silicones.
  • liquid rubbers e.g. low molecular weight nitrile or polyisoprene rubbers
  • liquid polymers of butene and/or isobutene e.g. low molecular weight nitrile or polyisoprene rubbers
  • acrylic acid esters e.g. low molecular weight nitrile or polyisoprene rubbers
  • acrylic acid esters e.g. low molecular weight nitrile or
  • Plasticizers from renewable raw materials are particularly preferably used, such as bio-based polyoxytrimethylene glycol, vegetable oils, preferably refined vegetable oils such as rapeseed oil and soybean oil, fatty acids or fatty acid esters, or epoxidized vegetable oils, for example epoxidized soybean oil.
  • biodegradable plasticizers are used, preferably di- or poly-esters of citric acid or adipic acid.
  • the plasticizer in particular the biodegradable one, is more preferably used in amounts of up to 10% by weight (based on the total weight of the PSA), particularly preferably in amounts of up to 5% by weight (based on the total weight of the PSA) , very particularly preferably in amounts of up to 2.5 wt .-% (based on the total weight of the pressure-sensitive adhesive).
  • the addition of any plasticizers is in minor amounts up to 1% by weight is possible without the biodegradability of the pressure-sensitive adhesive of the invention being lost.
  • Plasticizers are therefore preferably dispensed with, or biodegradable plasticizers are used.
  • the pressure-sensitive adhesive of the invention can comprise at least one further polymer (B) which is different from the polyhydroxyalkanoate(s) and is likewise a polyester.
  • the polyester (B) can be another polyhydroxyalkanoate, but also a polyester other than a polyhydroxyalkanoate.
  • the pressure-sensitive adhesive of the invention can be prepared in any manner conceivable for the person skilled in the art.
  • the components can simply be dispersed and mixed in a solvent, which is then removed.
  • the PSA of the invention can also be obtained from the melt.
  • the components are melted and mixed in the melt or partly incorporated into the melt of the copolymer.
  • the invention relates to a process for producing a pressure-sensitive adhesive according to the invention, which comprises the melting of at least one polyhydroxyalkanoate which comprises o to 20 to 70% by weight of structural units which can be traced back to 3-hydroxybutyric acid (3-HB); and o comprises at least one further structural unit which reacts to an acid selected from the group consisting of 4-hydroxybutyric acid (4-HB), 3-
  • the process is carried out in particular at low temperatures, preferably at less than 60°C, in particular at less than 50°C and very particularly preferably at less than 40°C. In particular, this also enables the incorporation of temperature-sensitive substances, e.g. proteins.
  • the other potential components of the PSA of the invention described herein can also be incorporated, in particular homogeneously, into the melt.
  • the multilayer composite system is an overlay for bonding to the skin (hereinafter also “skin overlay” or “overlay”), preferably human skin.
  • skin overlay or “overlay”
  • Pads according to the invention thus offer access to biodegradable skin pads that meet all adhesive and medical requirements.
  • the carrier material preferably consists of an air and water vapor permeable but water-impermeable polymer layer with a thickness of about 10 to 200 p.m.
  • backing materials which, after application of the adhesive, can be used in such a way that they meet the requirements for a functional skin contact.
  • Textiles such as wovens, knits, scrims or fleeces, further nets, foils, foams and laminates made from the above materials and papers may be mentioned by way of example.
  • the carrier material is preferably a film, a woven fabric or a fleece, particularly preferably with a thickness of 20 to 200 ⁇ m, in particular with a weight per unit area of 20 to 200 g/m 2 .
  • Common pre-treatments are plasma or corona treatment and hydrophobing;
  • Common post-treatments are calendering, tempering, laminating, punching, covering and sterilizing.
  • the carrier material is particularly preferably a polyurethane film, a polyethylene film, a polyester fleece, a woven fabric made from viscose, polyester or cotton or a woven fabric made from any mixtures of viscose, polyester and/or cotton.
  • the pressure-sensitive adhesive of the invention can be applied to the backing material by conventional methods. It is usually covered on one side with the carrier material, and the structure created in this way is applied as a composite. Depending on the substrate used, the moisture vapor transmission rate, strength of a wound dressing, cushioning against pressure, and other physical properties of the dressing can be controlled.
  • the skin dressing may also include a substrate for absorbing wound exudate.
  • the pad can basically be used as a full-surface self-adhesive or partial self-adhesive skin pad (dressing), in particular as a wound pad, plaster, hygiene item, cosmetic and/or dermatological pad, patch, tape, bandage, colostomy bag, fixation bandage, kinesio tape, cataplasma, bandage, Surgical cover or mask be designed.
  • the overlay is preferably a patch.
  • it can also be in the form of a less adhesive patch or pad, for example, with the adhesive strength being able to be set specifically according to the particular application.
  • the pressure-sensitive adhesive of the invention is preferably present in the overlay as a layer with a layer thickness of up to 120 gm, particularly preferably up to 100 gm, in particular up to 80 gm.
  • the general expression “adhesive tape” includes all flat structures such as tapes or tape sections extended in two dimensions, tapes with extended length and limited width, diecuts, labels and the like.
  • the adhesive tape can be made available in fixed lengths such as by the meter or as endless goods on rolls (Archimedean spiral) or as cross-wound spools. A layer or optionally several layers of adhesive can be applied to one or both sides of the carrier material.
  • the backing materials used for the adhesive tape are the usual backing materials familiar to the person skilled in the art, such as paper, fabric, fleece or foils, the latter made, for example, from polyesters such as polyethylene terephthalate (PET), polyethylene, polypropylene, stretched polypropylene or polyvinyl chloride.
  • PET polyethylene terephthalate
  • the carrier material is particularly preferably based on renewable raw materials such as paper, fabrics made from, for example, cotton, hemp, yurt, nettle fibers or bio-based and/or biodegradable polymers, for example polylactic acid.
  • the backing material can be provided with a pressure-sensitive adhesive on one or both sides.
  • both pressure-sensitive adhesives are preferably pressure-sensitive adhesives of the invention.
  • the adhesive tape is preferably formed by applying the pressure-sensitive adhesive to some or all of the surface of the backing.
  • the coating can also take place in the form of one or more strips in the longitudinal direction (machine direction), optionally in the transverse direction, but in particular it is all-over.
  • the PSA can be applied in grid dot form by screen printing, in which case the adhesive dots can also be of different sizes and/or distributed differently, by gravure printing in longitudinally and transversely connected webs, by grid printing or by flexographic printing.
  • the pressure-sensitive adhesive can be in the form of a dome (produced by screen printing) or else in another pattern, such as a grid, stripes, or zigzag lines. Furthermore, it can also be sprayed on, for example, which results in an irregular application pattern.
  • the coating thickness of the PSA is preferably between 10 and 200 g/m 2 , more preferably between 15 and 75 g/m 2 and particularly preferably between 20 and 50 g/m 2 .
  • Flame treatment, corona or plasma treatment, for example, are suitable as physical surface treatments.
  • the carrier material can be subjected to an anti-adhesive physical treatment or coating on the rear or top side, ie opposite the adhesive side, in particular equipped with a release agent or release system (if appropriate mixed with other polymers).
  • a release agent or release system if appropriate mixed with other polymers.
  • separating or - synonymous referred to - release layers are those made of stearyl compounds, for example polyvinylstearyl carbamate, stearyl compounds of transition metals such as Cr or Zr, ureas of polyethyleneimine and stearyl isocyanate; or from polysiloxanes.
  • stearyl is a synonym for all straight or branched alkyl or alkenyl radicals with a carbon number of at least 10, such as an octadecyl radical.
  • Suitable release agents also include surface-active release systems based on long-chain alkyl groups such as stearyl sulfosuccinates or stearyl sulfosuccinamates, but also polymers selected from the group consisting of polyvinyl stearyl carbamates, polyethyleneimine stearyl carbamates, chromium complexes of C14 to C28 fatty acids and stearyl copolymers. Release agents based on acrylic polymers with perfluorinated alkyl groups, silicones, for example based on polydimethylsiloxanes, and fluorosilicone compounds are also suitable.
  • the stimulation is particularly preferably an electronic stimulation, e.g. an electronic muscle stimulation (electronic muscle stimulation (EMS)).
  • EMS electronic muscle stimulation
  • the structure of the medical system can in particular include a protective layer, one or more adhesive intermediate layers, one or more stamped parts, one or more insulating layers, in particular against electromagnetic radiation or interference (EMI shielding), and one or more sensors.
  • a protective layer one or more adhesive intermediate layers, one or more stamped parts, one or more insulating layers, in particular against electromagnetic radiation or interference (EMI shielding), and one or more sensors.
  • EMI shielding electromagnetic radiation or interference
  • a further subject of the invention is the use of a pressure-sensitive adhesive of the invention as an adhesive for producing bonds on the skin, in particular on human skin.
  • the adhesive of the invention can be used in particular in an overlay for bonding to the skin or in a medical device that can be worn on the skin, in each case as set out above.
  • the details of the number-average molar mass M n and the weight-average molar mass M w in this document relate to the determination by gel permeation chromatography (GPC), which is known per se. The determination is carried out on a 100 ml sample that has been filtered clear (sample concentration 4 g/l). Tetrahydrofuran with 0.1% by volume of trifluoroacetic acid is used as the eluent. The measurement takes place at 25 °C.
  • the calibration is carried out using the commercially available ReadyCal kit poly(styrene) high from PSS Polymer Standard Service GmbH, Mainz.
  • the values are universally converted to polymethyl methacrylate (PMMA) using the Mark-Houwink parameters K and alpha, so that the data are given in PMMA mass equivalents.
  • the adhesive strength was determined in a test atmosphere of 23 °C +/- 1 °C temperature and 50% +/- 5% rel. humidity.
  • the samples were cut to 20mm width and glued to a steel plate (ASTM).
  • the steel plate was cleaned and conditioned before the measurement. For this purpose, the plate was first wiped with solvent and then left in the air for 5 minutes so that the solvent could evaporate.
  • the side of the adhesive tape facing away from the test substrate was then covered with 25 ⁇ m thick, etched PET film, which prevented the sample from stretching during the measurement.
  • the test sample was then rolled onto the substrate. For this purpose, the tape was rolled back and forth five times with a 4 kg roller at a winding speed of 10 m/min. 1 min after rolling, the plate was pushed into a special holder.
  • the shear strength was determined in a test climate of 23 +/- 1 °C temperature and 50% +/- 5% rel. humidity.
  • test samples were cut to a width of 13 ⁇ 0.2 mm and stored in a climatic environment for at least 16 hours.
  • 50 x 25 mm ASTM steel plates with a thickness of 2 mm and a 20 mm marking line were used, which were intensively cleaned several times with acetone before bonding and then left to dry for 10 minutes.
  • the bond area was 13 x 20 ⁇ 0.2 mm.
  • the test strip was applied to the middle of the substrate by rubbing it with a wiper in the longitudinal direction, avoiding air pockets, so that the upper edge of the test sample lay exactly on the 20 mm marking line.
  • An adapter plate was then attached to the front of the shear test panel with a screw and nut. To ensure that the adapter plate was firmly seated on the plate, the screw was tightened firmly by hand.
  • the pull-up time between rolling and loading was 12 minutes. The time in minutes before the bond failed was measured; the measurement results are the average of three measurements. A shearing life of at least 5,000 minutes is considered a good result.
  • the constituents for producing the PSAs were initially taken in the amounts stated in Table 2 in ethyl acetate (solids content 15%) and stirred at 45° C. for 3 hours. The resulting solution was then homogenized overnight using a roller bench. The dispersions obtained were applied to backings (etched PET film, 23 gm thick), the solvent was removed and the sheet-like PSAs obtained in this way (layer thickness 25 gm) were left to stand for one day in a test atmosphere. Then the tests were carried out.
  • the PSAs of Examples 1-3 were all biodegradable according to DIN EN 13432.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biomedical Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Dermatology (AREA)
  • Engineering & Computer Science (AREA)
  • Medicinal Chemistry (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Polymers & Plastics (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Materials For Medical Uses (AREA)
PCT/EP2022/066925 2021-06-21 2022-06-21 Biologisch abbaubare haftklebemasse WO2022268837A1 (de)

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EP22735868.6A EP4359463A1 (de) 2021-06-21 2022-06-21 Biologisch abbaubare haftklebemasse
AU2022299275A AU2022299275A1 (en) 2021-06-21 2022-06-21 Biodegradable pressure-sensitive adhesive

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DE102021206354 2021-06-21
DE102021206354.3 2021-06-21

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PCT/EP2022/066925 WO2022268837A1 (de) 2021-06-21 2022-06-21 Biologisch abbaubare haftklebemasse

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US5169889A (en) * 1992-01-27 1992-12-08 National Starch And Chemical Investment Holding Corporation Poly hydroxybutyrate/hydroxyvalerate based hot melt adhesive
US20040220355A1 (en) * 2003-02-21 2004-11-04 Whitehouse Robert S. PHA blends
EP1601737B1 (en) * 2003-02-21 2007-10-31 Metabolix, Inc. Pha adhesive compositions
EP2305324A1 (en) 1999-03-25 2011-04-06 Metabolix, Inc. Medical devices and applications of polyhydroxyalkanoate polymers
CN102867459A (zh) 2011-11-07 2013-01-09 中国印刷科学技术研究所 可生物降解不干胶标签
WO2015189323A1 (de) 2014-06-11 2015-12-17 Tesa Se Polyester-polyurethan

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5169889A (en) * 1992-01-27 1992-12-08 National Starch And Chemical Investment Holding Corporation Poly hydroxybutyrate/hydroxyvalerate based hot melt adhesive
EP2305324A1 (en) 1999-03-25 2011-04-06 Metabolix, Inc. Medical devices and applications of polyhydroxyalkanoate polymers
US20040220355A1 (en) * 2003-02-21 2004-11-04 Whitehouse Robert S. PHA blends
EP1601737B1 (en) * 2003-02-21 2007-10-31 Metabolix, Inc. Pha adhesive compositions
CN102867459A (zh) 2011-11-07 2013-01-09 中国印刷科学技术研究所 可生物降解不干胶标签
WO2015189323A1 (de) 2014-06-11 2015-12-17 Tesa Se Polyester-polyurethan

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Title
SATAS: "Handbook of Pressure Sensitive Adhesives Technology", 1999

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