WO2017100085A1 - Stratifié, kit adhésif, structure stratifiée et procédé de production de celle-ci, et composition adhésive de contact - Google Patents

Stratifié, kit adhésif, structure stratifiée et procédé de production de celle-ci, et composition adhésive de contact Download PDF

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Publication number
WO2017100085A1
WO2017100085A1 PCT/US2016/064540 US2016064540W WO2017100085A1 WO 2017100085 A1 WO2017100085 A1 WO 2017100085A1 US 2016064540 W US2016064540 W US 2016064540W WO 2017100085 A1 WO2017100085 A1 WO 2017100085A1
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WO
WIPO (PCT)
Prior art keywords
contact adhesive
microspheres
adhesive layer
mass
laminate
Prior art date
Application number
PCT/US2016/064540
Other languages
English (en)
Inventor
Hidetoshi Abe
Yuji Kashiwazaki
Mamoru Kanno
Original Assignee
3M Innovative Properties Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from JP2015239631A external-priority patent/JP6838857B2/ja
Application filed by 3M Innovative Properties Company filed Critical 3M Innovative Properties Company
Priority to EP16822786.6A priority Critical patent/EP3387082A1/fr
Priority to CN201680071674.8A priority patent/CN108368386A/zh
Priority to US15/780,312 priority patent/US20180273812A1/en
Publication of WO2017100085A1 publication Critical patent/WO2017100085A1/fr
Priority to US17/691,846 priority patent/US20220194053A1/en

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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
    • C09J5/00—Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers
    • C09J5/04—Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers involving separate application of adhesive ingredients to the different surfaces to be joined
    • 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
    • C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/20—Adhesives in the form of films or foils characterised by their 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
    • 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
    • C09J2411/00—Presence of chloroprene
    • 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
    • C09J2433/00—Presence of (meth)acrylic polymer

Definitions

  • the present disclosure relates to a laminate having a contact adhesive layer, an adhesive kit, a laminated structure, a production method of such a laminated structure, and a contact adhesive composition.
  • Decorative sheets are used for decorating interior or exterior walls, furniture or automobiles. These decorative sheets typically have pressure-sensitive adhesive layer on a back surface and they are applied to the adhered via the pressure sensitive adhesive layers. It is often difficult to apply the decorative sheet on an accurate position because of tackiness of the pressure sensitive adhesive layer. Therefore, it has been developed technology of controlling the tackiness of the pressure sensitive adhesive layer.
  • a pressure-sensitive adhesive layer having, on at least one surface thereof, a layer of evenly dispersed non-adhesive solid particles having an average particle diameter of 10 to 60 microns, wherein at least about half of the solid particles proj ect from the surface of the adhesive layer to a height corresponding to at least about one-fourth of the average particle diameter of the solid particles, and if the solid particles are hollow particles, the walls of the hollow particles are not rupturable by the pressure of bonding.
  • the pressure- sensitive adhesive layer has a very low initial adhesion strength (adhesion strength before press-bonding). After press-bonding, it rapidly develops adhesion strength, and attains a very high final adhesion strength"
  • US5795636 describes "An adhesive sheet having an adhesive layer and at least one surface being topologically microstructured, either with configured structures or a coating of particles and an underlying adhesive such that the adhesive layer has at least two levels of adhesion, a contact bond and an application bond, such that initial contact bond is substantially less than the application bond and that the contact bond simultaneously changes to the application bond with the application of pressure onto the adhesive sheet.”
  • JP4049450B describes "an aqueous contact adhesive formed by heat- melting, in the presence of an alkaline substance, a low acid-value tackifier resin that is solid at room temperature and that has a softening point of 100°C or lower, in a liquid containing a chloroprene rubber latex obtained by copolymerizing an ethylene-based unsaturated carboxylic acid that is copolymerizable with
  • chloroprene and chloroprene in the presence of polyvinyl alcohol or a chloroprene rubber latex obtained by copolymerizing an ethylene-based unsaturated carboxylic acid that is copolymerizable with chloroprene and chloroprene in the presence of polyvinyl alcohol and glycol ethers" .
  • the adhesive layer is a contact adhesive containing a plurality of beads.
  • the shape and sizing of the beads, and the ratio of beads to contact adhesive is selected such that the presence of the beads in the adhesive layer effects a plurality of protrusions from the adhesive layer.
  • the protrusions prevent aggressive bonding of between the adhesive layer and an installation substrate, and allow the adhesive-backed laminate construction to slide over an installation surface, effecting good repositionability during the installation process. Once positioning of the adhesive-backed laminate is satisfactory, the position may be finally set by pressing the adhesive-backed laminate against the installation surface.
  • Decorative adhesive-backed films have typically required the use of a release liner.
  • the release liner protects the adhesive layer during manufacturing and transport, and is removed at the time of installation, revealing the adhesive surface of the adhesive-backed laminate. It is later discarded. Besides being wasteful, the presence a release liner can introduce difficulties into the application process, particularly for large sheets of decorative film, for which the liner removal may be complicated and give rise to wrinkles in the installed laminate.
  • the present disclosure provides a contact adhesive-backed laminate construction having a low tack adhesive surface that may preclude, in some embodiments, the need for a traditional liner. The low tack adhesive surface may exhibit good slidability and repositionability during application. Upon further pressing of the adhesive securely bonds to the application substrate.
  • Adhesive kit embodiments are also described, which additionally involve the use of a primer adhesive layer applied to the installation substrate before installation of the adhesive-backed laminate.
  • a laminate construction comprising a substrate layer; a contact adhesive layer containing a contact adhesive agent containing at least one of chloroprene rubber or acrylic copolymers, and
  • microspheres having an average particle size of 0.5 ⁇ or greater in the contact adhesive layer, wherein the contact adhesive layer contains from 5 parts by mass to 500 parts by mass of the microspheres per 100 parts by mass of the contact adhesive agent, and wherein the contact adhesive layer has a plurality of protruding microsphere portions.
  • Another embodiment described herein concerns a film-based article comprising the laminate recited above and a primer agent containing a second contact adhesive agent containing at least one of chloroprene rubber or acrylic copolymers.
  • Yet another embodiment described herein concerns a method of applying a laminated structure to an installation surface, the method comprising preparing the laminate described above; applying a primer agent containing a second contact adhesive agent containing at least one of chloroprene rubber or acrylic copolymers on a installation surface so as to form a second contact adhesive layer, and placing the laminate on the second contact adhesive layer, and then pressing (and thereby adhering) the contact adhesive layer of the laminate to the second contact adhesive layer.
  • Yet another embodiment described herein concerns a laminated structure formed on a base material to be adhered comprising the laminate recited above, and a second contact adhesive layer covered on the installation surface, wherein both of the contact adhesive layer of the laminate and the second contact adhesive layer are adhered to each other, the second contact adhesive layer containing a second contact adhesive agent containing at least one of chloroprene rubber or acrylic copolymers.
  • a contact adhesive composition comprising a contact adhesive agent containing at least one of chloroprene rubber or acrylic copolymers, and microspheres having an average particle size of 0.5 ⁇ or greater, and further comprising from 5 parts by mass to 500 parts by mass of the organic resin microspheres per 100 parts by mass of the contact adhesive agent.
  • a protective liner may not be necessary.
  • the laminate of the present disclosure can be produced, stored, and transported as a continuous roll of film, or as a stack of a film sheets. This eliminates waste and money associated with the use of liners.
  • the surface of the adhesive layer of the laminate of the present disclosure provides good slidability, positioning, and repositioning
  • the laminate may be adhesively set pressing, with a roller or one's hand, the laminate onto the installation substrate.
  • the adhesive kit of the present disclosure contains the laminate as described above, and additionally includes a primer agent that is suitable for the contact adhesion of the laminate, thus providing good slidability and better contact adhesion of the laminate upon installation.
  • the primer is applied to the installation surface before the laminate.
  • the contact adhesive composition of the present disclosure can be suitably used in the production of the laminate described above.
  • FIG. 1 is a cross sectional view of a laminate of an embodiment of the present invention.
  • FIG. 2 is a drawing for explaining the method of producing a laminated structure of an embodiment of the present disclosure.
  • FIG. 3 is a cross sectional view of a laminated structure.
  • FIG. 4A and 4B are for explaining the method of installing flooring panels using a laminated structure of an embodiment of the present disclosure.
  • the laminate of an embodiment of the present disclosure comprises a substrate layer; a contact adhesive layer comprising a contact adhesive agent containing at least one of chloroprene rubber or acrylic copolymers, and
  • microspheres having an average particle size of 0.5 ⁇ or greater in the contact adhesive layer, wherein the contact adhesive layer contains from 5 parts by mass to 500 parts by mass of the microspheres per 100 parts by mass of the contact adhesive agent.
  • the contact adhesive layer has a plurality of protrusions from its surface, effected by the presence of the microspheres in the adhesive layer.
  • contact adhesive refers to an adhesive which is typically applied to two surfaces to be adhered together, dried to form film adhesive layers, and brought into contact with pressure so as to form an immediate, durable bond.
  • microspheres refers to particles having diameters than several micrometers. In some preferred embodiments, they are sustainably spherical.
  • Substantially spherical means having a cross-sectional shape corresponding to that of a circle or an ellipse, or having a spherical surface.
  • the laminate of an embodiment of the present disclosure is illustrated as a cross sectional view in FIG. 1.
  • the laminate 10 illustrated in FIG. 1 has a substrate layer 12 and a contact adhesive layer 14, and the contact adhesive layer 14 has a contact adhesive agent 16 and organic resin microspheres 18.
  • the microspheres 18 are illustrated as being completely covered by the contact adhesive agent 16; however, a part of the microspheres 18 may be exposed to the outside.
  • the microspheres 18 are illustrated as separate particles arranged regularly; however, a plurality of the microspheres 18 may be agglomerated, or a single or a plurality of agglomerated microspheres 18 may be arranged irregularly on the surface of the contact adhesive layer. There are a plurality of protruding portions because of the existing of the microspheres on a surface of the laminate 10.
  • the substrate layer may be selected from various materials and articles depending on the purpose thereof.
  • the substrate layer include paper, transparent films, decorative films, decorative plates, wallpaper, flooring materials, metal plates, woven fabric, nonwoven fabric, foam, and the like.
  • the substrate layer may be a laminate composed of a plurality of layers.
  • the substrate layer may also be a part of an article having a substrate layer, such as a part of a decorative sheet.
  • each of the substrate layer and the adherend may be a part of one article, such as a flap and a corresponding surface of an envelope.
  • the substrate layer may have undergone surface treatment, such as primer treatment or corona treatment, on a bonding face for the contact adhesive layer.
  • the contact adhesive layer may have a plurality of protruding portions and a surface that is substantially nontacky at operating temperature (typically room temperature).
  • substantially nontacky at room temperature refers to a condition where an adherend can be removed with no or substantially no resistance that can be felt by hands after the adherend was pressed lightly on the surface of the contact adhesive layer at 23°C ⁇ 0.5°C. In this condition, if the contact adhesive is lightly pressed onto an installation surface directly, as would occur during initial positioning of a laminate during an installation, the contact adhesive does not adhere to the installation surfaceat all, or if there is adhesion it is very light and easily succumbs to an installer's further maneuvering.
  • a plurality of protruding portions of the contact adhesive layer formed due to the microspheres 18 makes the surface of the contact adhesive layer rough.
  • the degree of the surface roughness of the contact adhesive layer can be evaluated by, for example, a 60 degree gloss value.
  • the 60 degree gloss value of the contact adhesive layer surface is approximately 1 or greater, approximately 2 or greater, or approximately 3 or greater, but approximately 40 or less, approximately 35 or less, or approximately 30 or less, when measured in accordance with Japanese Industrial Standard Z8741 or ISO 2813.
  • a part of the contact adhesive layer that interfaces with the installation surface may be covered by another material, such as printing ink or metal thin film, so long as it does not unduly interfere with the performance of the contact adhesive.
  • the contact adhesive layer also serves as a receiving layer of printing ink, such as ink for inkj et printing.
  • a liner may be arranged on the contact adhesive layer surface.
  • the contact adhesive layer surface can be protected from oils and fats, dust, or the like when the laminate is used as an intermediate product and is subj ected to further processing or treatment.
  • the contact adhesive agent is a component serving as a base of the contact adhesive layer.
  • the contact adhesive agent adheres to itself or to a chemically similar material by applying pressure without a significant increase in temperature (e.g. without requiring a temperature higher than 50°C). Therefore, unlike pressure-sensitive adhesive agent, the contact adhesive agent does not adhere to a chemically different material or shows little adhesive force to such a material, typically, at a temperature of approximately 10°C to approximately 50°C. On the other hand, the pressure-sensitive adhesive agents show tackiness at room
  • the contact adhesive agent contains at least one of chloroprene rubber or acrylic copolymers as an adhesive component.
  • the chloroprene rubber (CR) may be a homopolymer or copolymer of chloroprene (2-chloro-l,3-butadiene). Typically, a highly crystalline chloroprene rubber is used due to its excellent contact adhesion. Chloroprene rubber can be obtained by polymerizing chloroprene and, optionally, a copolymerizable monomer by solution polymerization, emulsion polymerization, suspension polymerization, or the like.
  • Examples of the copolymerizable monomer for chloroprene rubber include vinyl-based unsaturated monomers such as styrene, vinyltoluene, 2,3- dichlorobutadiene, acrylic acid, methacrylic acid, methacrylates, acrylates, acrylonitrile, vinyl acetate, and polyvinyl alcohol.
  • Chloroprene rubber may be crosslinked due to the double bond present in chloroprene rubber and a reaction caused by a crosslinking agent.
  • An acrylic copolymer can be obtained by copolymerizing alkyl acrylates having an alkyl group having from 1 to 8 carbons, alkoxy ethyl acrylates having an alkoxy group having from 1 to 4 carbons, acrylic acid, hydroxy group-containing acrylates, such as 2-hydroxyethyl acrylate, acrylic monomers, such as acrylamide, styrene, vinyltoluene, alkyl methacrylates having an alkyl group having from 1 to 8 carbons, such as methyl methacrylate and ethyl methacrylate, methacrylic acid, hydroxy group-containing methacrylates, such as 2-hydroxyethyl methacrylate, and other vinyl-based unsaturated monomers, such as methacrylamide, maleic acid, and itaconic acid, by solution polymerization, emulsion polymerization, suspension polymerization, or the like.
  • alkyl acrylate having an alkyl group having from 1 to 8 carbons examples include methyl acrylate, ethyl acrylate, n-butyl acrylate, 2-ethylhexyl acrylate, and the like.
  • alkoxy ethyl acrylate having an alkyl group having from 1 to 4 carbons examples include 2-methoxyethyl acrylate, 2- ethoxyethyl acrylate, 2-butoxyethyl acrylate, and the like.
  • the acrylic copolymer may be crosslinked.
  • the glass transition temperature of the acrylic contact adhesive is preferably approximately 0°C or higher, approximately 10°C or higher, or approximately 20°C or higher, but approximately 60°C or lower, approximately 50°C or lower, or approximately 40°C or lower.
  • Tg glass transition temperature
  • the contact adhesive agent may contain additional polymer components.
  • additional polymer component include natural rubber,
  • polybutadiene polyisoprene
  • ethylene-vinyl acetate copolymers polyvinyl acetate
  • polyvinyl acetate copolymers polyvinyl acetate copolymers
  • styrene-butadiene copolymers styrene-isoprene copolymers
  • butadiene-acrylonitrile copolymers polyurethane, polyvinylidene chloride, and the like, and combinations of these.
  • the additional polymer component is contained in the contact adhesive agent at an amount of approximately 5% by mass or greater, approximately 10% by mass or greater, or approximately 15% by mass or greater, but approximately 60% by mass or less, approximately 50% by mass or less, or approximately 40% by mass or less, in terms of solid content of the contact adhesive agent.
  • the contact adhesive agent may contain a tackifier.
  • a tackifier rosin derivatives, such as polymerized rosin and hydrogenated rosin, terpene-modified products, such as terpene resins and terpene phenol resins, coumarone-indene resins, aliphatic hydrocarbon resins, aromatic petroleum resins, phenol-based resins, styrene-based resins, xylene resins, and the like can be used.
  • the tackifier is contained in the contact adhesive agent at an amount of approximately 1% by mass or greater, approximately 2% by mass or greater, or approximately 5% by mass or greater, but approximately 50% by mass or less, approximately 30% by mass or less, or approximately 20% by mass or less, in terms of solid content of the contact adhesive agent.
  • the contact adhesive agent may further contain, as an optional component, an emulsifier, surfactant, and/or pH adjusting agent that are(is) used for emulsion polymerization or suspension polymerization of the adhesive component, a plasticizer, an antioxidant, a viscosity adjusting agent, a surfactant, a humectant, a UV absorbing agent, a photostabilizer, a pigment, a biocide, a preservative, a corrosion inhibitor, an inorganic filler, or the like.
  • the contact adhesive can be cross-linked.
  • the microspheres have an average particle size of approximately 0.5 ⁇ or greater.
  • the average particle size of the microspheres is defined as a volume average particle size (Dv) that can be measured by a laser diffraction scattering type particle size distribution analyzer.
  • a plurality of adhesive protrusions extend outward from the adhesive layer surface, thereby raising the adhesive layer surface somewhat, keeping it from making intimate contact with an installation surface (except in the presence of intentional pressure), and thereby making the surface substantially nontacky.
  • the plurality of the microspheres may be agglomerated in the contact adhesive layer. Such an agglomerate of the microspheres
  • the average particle size of the microspheres is
  • the average particle size is less than 0.3 ⁇ , it may be difficult to form the protruding portions based on the existing of the microspheres on the contact adhesive layer surface. If the average particle size is greater than 100 ⁇ , the protruding portions be unsuitably rough and thus be noticeable on final application.
  • the microspheres are preferably an organic resin.
  • the organic resin particles are relatively light compared to inorganic particles, the organic resin microspheres tend not to settle and can keep good dispersibility, when they are mixed with the contact adhesive. Eventually, the microspheres can be dispersed more uniformly in the contact adhesive layer.
  • specific gravity of the microspheres for the contact adhesive is approximately 0.9 or greater, approximately 1.0 or greater, or approximately 1.05 or greater, but approximately 1.50 or less, approximately 1.40 or less, or approximately 1.35 or less.
  • the density of the microspheres is within the range described above, slidability characteristics can be more uniformly imparted to the entire surface of the contact adhesive layer, by preventing extremely uneven distribution (e.g., precipitation) of the microspheres in the contact adhesive layer during the formation of the contact adhesive layer.
  • the microspheres are nontacky.
  • the nontackiness refers to a condition where microspheres have flowability at the operation temperature, typically at room temperature (23°C ⁇ 0.5°C). If nontacky
  • microspheres are used, microspheres can obtain the flowability among
  • slidability features can be more uniformly imparted to the entire surface of the contact adhesive layer by preventing extremely uneven distribution (e.g., precipitation) of the microspheres in the contact adhesive layer during the formation of the contact adhesive layer.
  • the microspheres may contain a polymer, such as an acrylic polymer (e.g. homopolymers and copolymers of alkyl acrylates such as polymethyl methacrylate and n-butyl acrylate, or the like), polycarbonate, polyurethane, polyester, and polystyrene. These polymers may be crosslinked.
  • the microspheres are preferably acrylic polymers, which show suitable dispersibility in the contact adhesive agent. Since the microspheres of crosslinked acrylic polymer are unlikely to be deformed due to its high hardness, the microspheres can impart even higher slidability to the contact adhesive layer. Further, it is preferably used crosslinked polymer for micorshereas to obtain solvent resistance and stable high elasticity for large temperature range.
  • the microspheres may be solid microspheres or hollow microspheres.
  • shell and core type particle can be used.
  • microspheres having the shell part made of urethane resin and the core part made of acrylic resin can be used.
  • the microspheres can be colored by pigments or dye.
  • Microspheres are preferably solid ones. Solid microspheres, typically more unlikely to be deformed under load , may impart even higher slidability
  • microspheres are preferably acrylic polymers, particularly preferably solid microspheres of crosslinked acrylic polymer, due to the high hardness and a good load bearing when being rolled up.
  • the shape of the microspheres is, in one embodiment, substantially spherical or spherical.
  • substantially spherical or spherical microspheres By using substantially spherical or spherical microspheres, as compared with non-spherical shapes, slidability of the contact adhesive layer can be further enhanced.
  • the microspheres preferably have high elasticity and are hard to deform.
  • the elastic modulus of the microspheres is approximately 2 x 10 6 Pa or greater, approximately 5 x 10 6 Pa or greater, or approximately lxl O 7 Pa or greater; but approximately 5xl 0 u Pa or less, approximately lxl O u Pa or less, or approximately 5xl 0 10 Pa or less.
  • the microspheres are contained in the contact adhesive layer at ratio of approximately 5 parts by mass to approximately 500 parts by mass per 100 parts by mass of the contact adhesive agent. In some embodiments, the microspheres are contained in the contact adhesive layer at a ratio of approximately 2 parts by mass or greater, approximately 5 parts by mass or greater, or approximately 8 parts by mass or greater; but approximately 550 parts by mass or less, approximately 500 parts by mass or less, or approximately 450 parts by mass or less, per 100 parts by mass of the contact adhesive agent.
  • a laminate having a contact adhesive with a plurality of protruding portions makes the surface of the contact adhesive layer substantially nontacky at room temperature, and provides good slidability during application of the laminate.
  • the laminate does not require a a protective liner.
  • a contact adhesive layer can be formed by using a contact adhesive composition comprising a contact adhesive agent containing at least one of chloroprene rubber or acrylic copolymers, and nontacky microspheres having an average particle size of approximately 0.5 ⁇ or greater, and containing from approximately 5 parts by mass to approximately 500 parts by mass of the microspheres per 100 parts by mass of the contact adhesive agent.
  • the components and the amounts contained in the contact adhesive composition are as described above for the contact adhesive layer.
  • the contact adhesive composition can be prepared by mixing the
  • microspheres into a solvent system, emulsion system, or solventless system composition containing at least one of chloroprene rubber or acrylic copolymers as an adhesive component, and other optional components, such as an additional polymer component, a tackifier, a plasticizer, and the like.
  • the solvent system composition include organic solvents such as methanol, ethanol, hexane, toluene, acetone, methyl ethyl ketone, and ethyl acetate, and combinations of these. From the perspectives of requiring no organic solvent treatment during the production step of the laminate and achieving excellent coatability, it is
  • the contact adhesive composition is an aqueous emulsion.
  • the solid content thereof can be set to, for example, approximately 20% by mass or greater, approximately 30% by mass or greater, or approximately 40% by mass or greater; but approximately 80% by mass or less, approximately 70% by mass or less, or approximately 60% by mass or less. By setting the solid content to be within the range described above, a composition having good coatability and drying property can be obtained.
  • the laminate of the present disclosure can be produced by applying the contact adhesive composition on a surface of a substrate layer and, as necessary, drying or curing it to form a contact adhesive layer on the substrate layer.
  • the application of the contact adhesive composition onto the substrate layer surface can be performed using, for example, knife coating, bar coating, blade coating, doctor coating, roll coating, cast coating, spraying, screen printing, stencil printing, brush coating, or the like.
  • composition such as coating speed, application temperature, coating thickness (wet thickness), and drying or curing conditions including for example drying or curing temperature, can be selected in a manner that the protruding portions are formed with sufficient density on the contact adhesive layer surface.
  • the contact adhesive composition is preferably applied on the substrate layer surface in a manner that the mass per unit area of the contact adhesive layer is approximately 5 g/m 2 or greater, approximately 10 g/m 2 or greater, or
  • the protruding portions can be formed on the entire surface of the contact adhesive layer with sufficient density and in-plane uniformity of the slidability can be enhanced.
  • the thickness of the contact adhesive layer can be set typically to
  • the protruding portions can be formed on the contact adhesive layer surface in a manner such that the microspheres are not completely embedded in the contact adhesive layer and protrude somewhat from, or sit proud of, the contact adhesive layer.
  • kits which is a
  • the kit could be sold to a customer.
  • the primer agent is used to form a second contact adhesive layer on the installation surface and contains a second contact adhesive agent containing at least one of chloroprene rubber or acrylic copolymers, and optionally, nontacky second microspheres having an average particle size of approximately 0.5 ⁇ or greater.
  • the microspheres are an optional component, and the components and the amounts of the microspheres contained in the primer agent are the same as those described for the contact adhesive composition.
  • the second contact adhesive agent and/or the second microspheres, which are an optional component, contained in the primer agent may be the same as or different from the contact adhesive agent (first contact adhesive agent) and/or the microspheres (first microspheres) contained in the contact adhesive layer (first contact adhesive layer) of the laminate.
  • substances having chemical properties that are similar to those of the adhesive component contained in the first contact adhesive agent and the adhesive component contained in the second contact adhesive agent i.e. both of the adhesive components in the first and second contact adhesive agents being chloroprene rubber or the both of the adhesive components being acrylic copolymers, even higher contact adhesion can be achieved.
  • the primer agent contains the second microspheres at an amount of approximately 2 parts by mass or greater, approximately 5 parts by mass or greater, or approximately 8 parts by mass or greater; but approximately 550 parts by mass or less, approximately 500 parts by mass or less, or approximately 450 parts by mass or less, per 100 parts by mass of the second contact adhesive agent.
  • the plurality of protruding portions formed on the surface of the second contact adhesive layer of the installation surface via application of the primer agent reduces the initial contact area of a laminate brought into contact with the prime installation surface, and thus the laminate can be more easily slid and positioned on the adherend surface.
  • shear adhesion can be enhanced by making the microspheres contained in the contact adhesive layer of the laminate and the microspheres in the second contact adhesive layer formed on the surface of the installation surface to engage each other when the laminate is adhered to the installation surface via further pressing (as by an installer's hand or via rollers or the like).
  • the substrate layer of the laminate is flexible like a decorative film
  • dimensional stability of the laminate may be enhanced by suppressing the in-plane shrinkage of the substrate layer due to the engaging of the microspheres.
  • Friction, and thus slideability, between the contact adhesive layer of the laminate and the the primer agent is a function of the total amount of the
  • the total of the amount (part by mass) of the microspheres (first microspheres) per 100 parts by mass of the contact adhesive agent (first contact adhesive agent) contained in the contact adhesive layer of the laminate and the amount (part by mass) of the second microspheres per 100 parts by mass of the second contact adhesive agent of the primer agent is approximately 5 parts by mass or greater, approximately 7 parts by mass or greater, or approximately 9 parts by mass or greater; but approximately 1100 parts by mass or less, approximately 1000 parts by mass or less, or approximately 900 parts by mass or less.
  • a method of producing a laminated structure is shown.
  • the method comprises the steps of preparing laminate 10; applying the primer agent on a surface of an installation surface 30 so as to form a second contact adhesive layer 20; and placing the laminate 10 on the second contact adhesive layer 20.
  • the laminate 10 can slide because of the plurality of protruding portions 18 on the contact adhesive layer 14, accordingly, the laminate 10 can be repositioned to an accurate position.
  • the laminate 10 can exhibit better slidability.
  • the contact adhesive layer 14 of the laminate 10 may be brought into more intimate contact with the second contact adhesive layer 20 by the installer applying pressure to successive portions of the laminate 10 onto the installation surface 30 so as to form a laminate structure shown in Fig.3.
  • pressure may be applied using techniques well known in the art, such as by pressing with a hand, roller, or the like.
  • Fig. 4A and Fig.4B show a method of installing floor materials such as flooring panels using an adhesive kit of the present disclosure.
  • Flooring panels typically have a protrusion on a side surface, and at installation they are positioned to mate with the a recess on the side surface of an adj acent material.
  • Flooring panels are often bonded to a carier material such as particle board, mortar, or the like, which is arranged on a floor of a building, in a manner that the flooring panels mates with an adj acent flooring panels.
  • a contact adhesive comprising a contact adhesive layer 116 having a plurality of protruding portion because of microspheres 118 can be formed on the substrate layer 116 of a flooring panel, and, meanwhile, a primer agent containing microspheres 124 can be applied on a surface of a floor 130 to form a second contact adhesive layer 122 on the floor 130 using an adhesive kit in this disclosure.
  • the contact adhesive layer 116 of the flooring panel 110 can slide smoothly, allowing for easy repositioning. Once the panels are in proper position, their position may be fixd by pressing with a pressure tool 140.
  • the installation surface may be, for example, a surface of a piece of furniture, such as bookshelf, cupboard, or chest, an inner wall or floor of a building, an inner wall or outer wall of an automobile or a railway vehicle, a surface of a household item. .
  • the application of the primer agent onto the installation surface can be performed in the same manner as for the application of the contact adhesive composition onto the substrate layer surface, as mentioned above. Examples include the use of knife coating, bar coating, blade coating, doctor coating, roll coating, cast coating, spraying, screen printing, stencil printing, brush coating, or the like. After the primer agent is applied to the installation surface, drying or curing may be performed as necessary.
  • the application conditions of the primer agent such as coating speed, application temperature, coating thickness (wet thickness), and drying or curing conditions including, for example, drying or curing temperature, can be selected in a manner that the protruding portions are formed with sufficient density on the second contact adhesive layer surface.
  • the pressure applied to the laminate can be set to, for example, approximately lk Pa or greater, approximately 5kPa or greater, or approximately 10 k Pa or greater; but approximately 1000k Pa or less, approximately 600k Pa or less, or approximately 200k Pa or less.
  • Positioning or repositioning of the laminate can be performed by sliding the laminate on the installation surface.
  • the lamination is typically performed at approximately 10°C or higher, or approximately 20°C or higher; but approximately 100°C or lower, or approximately 50°C or lower or approximately 1 second or longer, or approximately 3 seconds or longer; but approximately 60 mins or shorter, or approximately 30 mins or shorter.
  • an installed structure having the substrate layer, the first contact adhesive layer (contact adhesive layer of the laminate), the second contact adhesive layer (applied to the installation surface), and then the installation surface, in this order can be formed.
  • the first contact adhesive layer and the second contact adhesive layer have identical chemical composition, the interface between these adhesive layers, after the two layers are pressed together, may not be easily observed.
  • the laminate, the adhesive kit, and the contact adhesive composition of the present disclosure can be widely used for industrial purposes such as for interior and exterior of automobiles, railway vehicles, and the like, general household utensils, such as envelopes, as well as for housing and building purposes, including applications of a decorative sheet or decorative plate to furniture, such as bookshelf, cupboard, or chest, or to an inner wall of a building, installing interior building materials, such as flooring materials, on a floor of a building, or the like. Furthermore, use of protective liners processing paper, processing film, or the like during the production of a decorative sheet can be omitted, in some embodiments, by using the laminate of the present disclosure.
  • Acrylic Chemisnow (trademark) MX-500H 100 microspheres nontacky solid microspheres
  • Acrylic Chemisnow (trademark) MZ-10HN 100 microspheres nontacky solid microspheres
  • Acrylic Chemisnow (trademark) MZ-30H 100 microspheres nontacky solid microspheres
  • Primer 2 (P2) A mixed solution of A2 and B 1, Water
  • Primer 4 (P4) A mixed solution of A2 and B 1, Water
  • Primer 5 A mixed solution of Al and B 10, Water
  • the glass transition temperatures (Tg) of the adhesive agent 1 (Al) and the adhesive agent 2 (A2) were measured using an ARES dynamic viscoelasticity measuring device (manufactured by TA Instruments Japan Inc., Shinagawa-ku, Tokyo, Japan). Al or A2 was formed into a film having a dry thickness of 3 mm, and test samples having a diameter of about 7.9 mm were produced by punching out the film.
  • the adhesive agent 3 (A3) was prepared by the following procedure.
  • A3 was prepared as an ethyl acetate solution (solid content: 33%) by dissolving 94 parts by mass of n-butyl acrylate (BA) and 6 parts by mass of acrylic acid (AA) in 200 parts by mass of ethyl acetate, adding 0.2 parts by mass of 2,2'-azobis(2,4- dimethylvaleronitrile) (trade name: V-65, manufactured by Wako Pure Chemical Industries, Ltd., Osaka-shi, Osaka, Japan) as a polymerization initiator, and then reacting the mixture for 24 hours at 65°C in a nitrogen atmosphere.
  • BA n-butyl acrylate
  • AA acrylic acid
  • V-65 2,2'-azobis(2,4- dimethylvaleronitrile)
  • the weight average molecular weight (Mw) of A3 was 560,000, and the glass transition temperature (Tg) was -48°C.
  • the Tg was determined by the Fox equation (below equation) assuming that each polymer is formed by copolymerization of n types of monomers.
  • Tg2 Glass transition temperature of homopolymer of component 2
  • Tg n Glass transition temperature of homopolymer of component n
  • the test piece was cut into a length of 300 mm and a width of 210 mm.
  • the test piece had no release liner.
  • the test piece was wound around a 6-inch core and left at 23°C for 48 hours.
  • the test piece did not adhere to the embossed surface of the film and was easily peeled off, the test piece was evaluated as being "excellent” .
  • the test piece was slightly adhered to the embossed surface of the film but was peeled off, the test piece was evaluated as being "good” .
  • the test piece was firmly adhered to the embossed surface of the film but was peeled off without extending the film, the test piece was evaluated as being “fair " .
  • the test piece was firmly adhered to the embossed surface of the film and separation of these was difficult, the test piece was evaluated as being “poor” .
  • Two test pieces were prepared.
  • the adhesive layer face of the first test piece was lightly placed on the top of the face on which no adhesive agent was coated of the second test piece, at 23°C.
  • the case was evaluated as being "excellent” .
  • the case was evaluated as being "good” .
  • test piece was cut into a length of 150 mm and a width of 25 mm.
  • the adhesive layer face of the test piece was lightly brought into contact with the primer-treated face of plasterboard at 25°C.
  • the test piece was evaluated as being "excellent” .
  • the test piece was evaluated as being "good” .
  • the test piece was evaluated as being “poor” .
  • Two test pieces were prepared.
  • the adhesive layer face of the first test piece was placed on the top of the adhesive layer face of the second test piece without applying pressure at 23°C.
  • the case was evaluated as "good” .
  • the case was evaluated as being "poor” .
  • the test piece was cut into a length of 150 mm and a width of 25 mm.
  • the adhesive layer face of the test piece was pressure-adhered to the primer-treated face of plasterboard at 23 °C using a squeegee, and then left at 23 °C for 48 hours.
  • the adhesive force was measured in accordance with JIS Z 0237 8.2.3.
  • a tensile testing machine Teensilon universal testing machine, model : RTC-1210A, manufactured by A&D Company, Limited, Toshima-ku, Tokyo, Japan
  • 180° peel strength was measured at a peeling rate of 300 mm/min at 20°C.
  • peeling mode was for surface breakage of the plasterboard, and the peak value of the adhesive force was recorded as the representative value.
  • test pieces Two test pieces were prepared.
  • the adhesive layer face of the first test piece was placed on the top of the adhesive layer face of the second test piece and pressure-adhered using a squeegee in an environment at 23°C.
  • the test pieces were left for 5 minutes in an environment at 23°C. When the test pieces were firmly adhered, the case was evaluated as being “good” . When the test pieces were easily peeled, the case was evaluated as being “poor” .
  • the 60 Degree gloss values of contact adhesive layer were measured by portable gloss meter GMX-202 (Manufactured by Murakami Color Research Laboratory (Chuo-ku, Tokyo, Japan). The values were measured at three positions. Averaged value was calculated.
  • a contact adhesive composition was prepared by mixing the adhesive agent 1 (Al) and the acrylic microspheres 1 (B l). The mass ratio of Al and B l was 100: 10 in terms of solid content.
  • the contact adhesive composition was coated on a smooth surface of an embossed polyvinyl chloride (PVC) film having a thickness of about 170 ⁇ using a knife coater and dried for 4 minutes at 40°C. After the drying, a contact adhesive layer having a thickness of 16 ⁇ was obtained.
  • the contact adhesive layer had recesses and protrusions on the surface.
  • the coated amount of the contact adhesive layer was 23 g/m 2 .
  • the surface of the contact adhesive layer was substantially nontackey and it is unnecessary to cover the surface by a release liner.
  • the primer 1 (P I) was coated on a plasterboard using a brush.
  • the primer layer was dried for 1 hour at 23°C. After the drying, the coated amount of the primer layer was 35 g/m 2 .
  • the PVC film having the contact adhesive layer was pressure- adhered to the primer layer of the plasterboard using a squeegee at 23°C.
  • the evaluation results are also shown is Table 2.
  • test piece of Example 2 to 51 were produced in the same manner as in
  • Example 1 each formulation of adhesive and microspheres for the adhesive layer and primer condition, and manufacturing conditions are shown is Table 2. The evaluation results are also shown is Table 2. Comparative Example 1
  • a pressure-sensitive adhesive composition was prepared by mixing the adhesive agent 3 (A3) and the crosslinking agent 1 (CLl). The mass ratio of A3 and CLl was 100:0.1 in terms of solid content.
  • the pressure-sensitive adhesive composition was coated on a smooth surface of an embossed polyvinyl chloride (PVC) film having a thickness of 170 ⁇ using a knife coater and dried for 5 minutes at 95°C. After the drying, a pressure-sensitive adhesive layer having a thickness of 38 ⁇ was obtained. The coated amount of the pressure-sensitive adhesive layer was 46 g/m 2 . As the pressure-sensitive adhesive layer has high tackiness at room temperature, it was necessary to cover the surface of the adhesive layer by a release liner.
  • the primer 3 (P3) was coated on a plasterboard using a brush.
  • the primer layer was dried for 1 hour at 23°C.
  • the PVC film having the pressure-sensitive adhesive layer was pressure- adhered to the primer layer of the plasterboard using a squeegee at 23°C.
  • the evaluation results are shown is Table 3.
  • test piece of Comparative Examples 2 to 14 were produced in the same manner as in Example 1. However, each formulation of adhesive and microspheres for the adhesive layer and primer condition, and manufacturing conditions are shown is Table 3. The evaluation results are also shown is Table 3.
  • a contact adhesive composition was prepared by mixing the adhesive agent 1 (Al) and the acrylic microspheres 1 (B l). The mass ratio of Al and B l was 100:30 in terms of solid content.
  • the contact adhesive composition was coated on one face of a plywood board (150 mm x 70 mm x 1 mm thickness) using a brush, and dried at 23°C for 60 minutes. After the drying, the contact adhesive layer had recesses and protrusions on the surface. The coated amount of the contact adhesive layer was approximately 35 g/m 2 .
  • the evaluation results are shown in Table 4.
  • Example 2-2 The evaluation results are shown in Table 4.
  • Example 2-2 The test piece of Example 2-2 was produced in the same manner as in Example 2-1 except for changing the adhesive agent to the adhesive agent 2 (A2). Comparative Example 2-1 to 2-3
  • test piece of Comparative Example 2- 1 to 2-3 were produced in the same manner. However, each condition of the material compositions and evaluation results are shown in Table 4.
  • Second contact adhesive layer 20 Second contact adhesive layer 22 Second contact adhesive agent 24 Second organic resin microsphere 30 Adherend

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Adhesive Tapes (AREA)
  • Laminated Bodies (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

La présente invention concerne un stratifié comprenant une couche de substrat ; une couche adhésive de contact comportant un agent adhésif de contact comportant au moins l'un d'un caoutchouc chloroprène ou de copolymères acryliques, ainsi que des microsphères ayant une taille de particule moyenne de 0,5 µm ou plus dans la couche adhésive de contact, la couche adhésive de contact contenant de 5 parties en masse à 500 parties en masse des microsphères pour 100 parties en masse de l'agent adhésif de contact, et la couche adhésive de contact comportant une pluralité de parties saillantes en raison des microsphères.
PCT/US2016/064540 2015-12-07 2016-12-02 Stratifié, kit adhésif, structure stratifiée et procédé de production de celle-ci, et composition adhésive de contact WO2017100085A1 (fr)

Priority Applications (4)

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EP16822786.6A EP3387082A1 (fr) 2015-12-07 2016-12-02 Stratifié, kit adhésif, structure stratifiée et procédé de production de celle-ci, et composition adhésive de contact
CN201680071674.8A CN108368386A (zh) 2015-12-07 2016-12-02 层合物、粘合剂套件、层合结构及其制造方法，以及接触粘合剂组合物
US15/780,312 US20180273812A1 (en) 2015-12-07 2016-12-02 Laminate, adhesive kit, laminated structure and production method thereof, and contact adhesive composition
US17/691,846 US20220194053A1 (en) 2015-12-07 2022-03-10 Laminate, adhesive kit, laminated structure and production method thereof, and contact adhesive composition

Applications Claiming Priority (4)

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US201562264308P 2015-12-07 2015-12-07
US62/264,308 2015-12-07
JP2015239631A JP6838857B2 (ja) 2015-12-07 2015-12-08 積層体、接着キット、積層構造体及びその製造方法、並びにコンタクト接着剤組成物
JP2015-239631 2015-12-08

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US17/691,846 Continuation US20220194053A1 (en) 2015-12-07 2022-03-10 Laminate, adhesive kit, laminated structure and production method thereof, and contact adhesive composition

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US11407925B2 (en) 2017-04-10 2022-08-09 3M Innovative Properties Company Adhesive sheet and method of applying adhesive sheet to rough surface
WO2023006629A1 (fr) * 2021-07-26 2023-02-02 Tesa Se Matière auto-adhésive en forme de bande contenant du polyuréthane et/ou du silicone
TWI839787B (zh) 2021-07-26 2024-04-21 德商特薩歐洲股份公司 包含聚胺基甲酸酯系填料及/或聚矽氧系填料之帶狀壓敏性黏著劑、其製造方法及其用途

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EP0534393A1 (fr) * 1991-09-24 1993-03-31 Air Products And Chemicals, Inc. Colle de contact à haute performance contenant microsphères
US5795636A (en) 1995-11-15 1998-08-18 Minnesota Mining And Manufacturing Company Positionable and repositionable adhesive article
WO2001070897A2 (fr) * 2000-03-22 2001-09-27 The Procter & Gamble Company Feuille adhesive a resistance d'adhesion elevee, pouvant etre repositionnee
USRE37612E1 (en) * 1983-12-21 2002-03-26 Beiersdorf Ag Residuelessly redetachable contact-adhesive sheetlike structures
US20070224395A1 (en) * 2006-03-24 2007-09-27 Rowitsch Robert W Sprayable water-based adhesive
JP4049450B2 (ja) 1998-06-25 2008-02-20 コニシ株式会社 水性コンタクト接着剤
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USRE37612E1 (en) * 1983-12-21 2002-03-26 Beiersdorf Ag Residuelessly redetachable contact-adhesive sheetlike structures
US5008139A (en) 1987-10-31 1991-04-16 Nippon Carbide Kogyo Kabushiki Kaisha Pressure-sensitive adhesive layer
EP0534393A1 (fr) * 1991-09-24 1993-03-31 Air Products And Chemicals, Inc. Colle de contact à haute performance contenant microsphères
US5795636A (en) 1995-11-15 1998-08-18 Minnesota Mining And Manufacturing Company Positionable and repositionable adhesive article
JP4049450B2 (ja) 1998-06-25 2008-02-20 コニシ株式会社 水性コンタクト接着剤
WO2001070897A2 (fr) * 2000-03-22 2001-09-27 The Procter & Gamble Company Feuille adhesive a resistance d'adhesion elevee, pouvant etre repositionnee
US20070224395A1 (en) * 2006-03-24 2007-09-27 Rowitsch Robert W Sprayable water-based adhesive
US20080118693A1 (en) * 2006-11-17 2008-05-22 Bilski Lori A Method of making a microsphere transfer adhesive

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11407925B2 (en) 2017-04-10 2022-08-09 3M Innovative Properties Company Adhesive sheet and method of applying adhesive sheet to rough surface
WO2023006629A1 (fr) * 2021-07-26 2023-02-02 Tesa Se Matière auto-adhésive en forme de bande contenant du polyuréthane et/ou du silicone
TWI839787B (zh) 2021-07-26 2024-04-21 德商特薩歐洲股份公司 包含聚胺基甲酸酯系填料及/或聚矽氧系填料之帶狀壓敏性黏著劑、其製造方法及其用途

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