EP3116964A1 - Article adhésif pouvant être enlevé par étirement, utilisation et fabrication de cet article - Google Patents

Article adhésif pouvant être enlevé par étirement, utilisation et fabrication de cet article

Info

Publication number
EP3116964A1
EP3116964A1 EP14885414.4A EP14885414A EP3116964A1 EP 3116964 A1 EP3116964 A1 EP 3116964A1 EP 14885414 A EP14885414 A EP 14885414A EP 3116964 A1 EP3116964 A1 EP 3116964A1
Authority
EP
European Patent Office
Prior art keywords
adhesive tape
weight percent
stretch releasable
releasable adhesive
polyurethane
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP14885414.4A
Other languages
German (de)
English (en)
Other versions
EP3116964A4 (fr
Inventor
Jun Li
Jingjing Ma
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.)
3M Innovative Properties Co
Original Assignee
3M Innovative Properties Co
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 3M Innovative Properties Co filed Critical 3M Innovative Properties Co
Publication of EP3116964A1 publication Critical patent/EP3116964A1/fr
Publication of EP3116964A4 publication Critical patent/EP3116964A4/fr
Withdrawn legal-status Critical Current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
    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/20—Adhesives in the form of films or foils characterised by their carriers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/04—Interconnection of layers
    • B32B7/06—Interconnection of layers permitting easy separation
    • B—PERFORMING OPERATIONS; TRANSPORTING
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    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B—PERFORMING OPERATIONS; TRANSPORTING
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    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • B—PERFORMING OPERATIONS; TRANSPORTING
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    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
    • B32B27/26—Layered products comprising a layer of synthetic resin characterised by the use of special additives using curing agents
    • B—PERFORMING OPERATIONS; TRANSPORTING
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    • B32B27/28—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
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    • B32B27/28—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
    • B32B27/288—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42 comprising polyketones
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    • B32B7/04—Interconnection of layers
    • B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
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    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
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    • C08G18/40—High-molecular-weight compounds
    • C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
    • C08G18/6216—Polymers of alpha-beta ethylenically unsaturated carboxylic acids or of derivatives thereof
    • C—CHEMISTRY; METALLURGY
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    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/78—Nitrogen
    • C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
    • C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
    • C08G18/792—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/83—Chemically modified polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04—Polyurethanes
    • C08L75/06—Polyurethanes from polyesters
    • 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
    • C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
    • C09J175/04—Polyurethanes
    • 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
    • C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
    • C09J175/04—Polyurethanes
    • C09J175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/20—Adhesives in the form of films or foils characterised by their carriers
    • C09J7/22—Plastics; Metallised plastics
    • C09J7/25—Plastics; Metallised plastics based on macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
    • 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
    • C09J7/00—Adhesives in the form of films or foils
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    • C09J7/381—Pressure-sensitive adhesives [PSA] based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C09J7/385—Acrylic polymers
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    • C—CHEMISTRY; METALLURGY
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    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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    • 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
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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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    • C—CHEMISTRY; METALLURGY
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    • C—CHEMISTRY; METALLURGY
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    • C—CHEMISTRY; METALLURGY
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    • C—CHEMISTRY; METALLURGY
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    • C09J2475/00—Presence of polyurethane
    • C09J2475/006—Presence of polyurethane in the substrate

Definitions

  • the present invention relates to adhesive tapes, more particularly to a stretch releasable adhesive tapes.
  • Adhesive tapes such as, for example, pressure-sensitive adhesive tapes
  • U.S. Pat. No. 6,527,900 discloses a removable adhesive tape that can be applied to a substrate. The adhesive tape becomes firmly bonded after being attached to the substrate, but can be easily removed without damaging the substrate by simply stretching it in a direction substantially parallel, i.e., less than about 35 ° degree, to the surface of the substrate. In some occasions, it will not be workable to remove such an adhesive tape from a direction parallel or less than 35 ° degree if the tape is used in a highly compacted electronic device, for example, a mobile phone to adhere an inside placed battery with its recessed substrate.
  • a first aspect relates to a stretch releasable adhesive tape including a backing having a first surface and a second surface, the backing being made of cross-linked thermoplastic polyurethane, and a pressure sensitive adhesive disposed on at least one of the first and second surfaces.
  • the pressure sensitive adhesive is formed from an acrylic copolymer comprising a functional group terminated polyurethane.
  • the adhesive tape has a thickness ranged between 0.05 and 0.10mm and a lengthwise elongation at break ranged between 850% and 2200%, the adhesive tape being capable of being firmly bonded to a substrate and thereafter being removable therefrom after being stretched at an angle at 90° degree or greater degree from the surface of the substrate without rupturing prior to the removal of the adhesive tape from the substrate and without leaving substantial pressure-sensitive adhesive residue on the substrate.
  • a second aspect relates to a A stretch releasable adhesive tape including a substrate having a first surface and a second surface, wherein the substrate includes cross-linked thermoplastic polyurethane and a pressure sensitive adhesive disposed on at least one of the first and second surfaces, wherein the pressure sensitive adhesive is formed from a reaction mixture comprising:
  • a third aspect relates to a stretch releasable adhesive tape being capable of being firmly bonded to a substrate and thereafter being removable therefrom after being stretched at an angle at 90° or greater degree from the surface of the substrate without leaving residue.
  • the tape includes a backing layer having a first and second opposed major surfaces, wherein the backing layer comprises cross-linked polyurethane;
  • acrylic copolymer adhesive disposed on at least one of the first and second opposed major surfaces; wherein the acrylic adhesive comprises functional group terminated polyurethane polymer to increase bonding with the backing layer such that the cohesion between the backing layer and adhesive is greater than adhesion between the substrate and the adhesive.
  • a fourth aspect relates to a stretch releasable adhesive tape including a backing and a first layer of a pressure-sensitive adhesive composition coated on at least one surface of said backing, the adhesive tape having a thickness between 0.05 and 0.10mm, and elongation at break between 850% and 2200%) , being capable of being firmly bonded to a substrate and thereafter being removable therefrom after being stretched at an angle at 90°degree or greater degree from the surface of a substrate without rupturing prior to the removal of the tape from the substrate and without leaving substantial pressure-sensitive adhesive residue on the substrate, wherein the pressure sensitive adhesive contains a functional group terminated polyurethane.
  • An electronic device comprising a stretch releasable adhesive tape of the invention is also described.
  • a fifth aspect relates to a method of making a stretch releasable adhesive tape.
  • the method includes making a modified acrylic copolymer, making a cross-linked polyurethane layer, and then coating the modified acrylic copolymer on the polyurethane layer.
  • the process of making modified acrylic copolymer includes preparing acrylic adhesive solution by mixing acrylic copolymer and functional group terminated polyurethane; providing a mixture of a cross-linking agent with the acrylic adhesive solution; coating the mixture on a liner; and curing the liner to form an adhesive layer by putting the coated liner into an oven.
  • the functional group terminated polyurethane may be selected from aliphatic sulfonic acid terminated polyurethane, or aromatic hydroxyl terminated polyurethane, or their combinations.
  • the process for making the polyurethane layer including the following steps of:
  • preparing a polyurethane solution by mixing aromatic polyester-based thermoplastic polyurethane with mehylethylketone; crosslinking the polyurethane solution; coating the polyurethane solution on a liner; and finally curing the liner under the condition of around 80°C for a predetermined period of time.
  • a stretch releasable adhesive tape can be used in many electronic devices.
  • An electronic device may be, for example, a cell phone, a personal assistance device, a music player such as, MP3, a MP4, and a laptop computer and so on.
  • the electronic device is intended to represent one desirable end use application for the stretch releasable adhesive article, but it will be recognized that the stretch releasable adhesive article may be used in a wide variety of other end-use
  • the electronic device may be a mobile phone.
  • the phone includes a battery, a battery receiving surface, and a stretch releasable adhesive article for releasably bonding the battery to the battery receiving surface.
  • a stretch force is applied to pull the adhesive tape out at an angle around 90°degree or greater degree from the battery surface. It is desirable that the stretch releasable adhesive article can removed without rupturing prior to the removal thereof from the battery surface and without leaving adhesive residue on the battery surface.
  • Fig. 1 shows an exemplary structure of a stretch releasable adhesive tape
  • Fig.2 shows an illustration of maximum bonding strength test being used to test the properties of the stretch releasable adhesive tape in Fig. 1;
  • FIG. 3 shows an illustration of stretch releasing test of the stretch releasable adhesive tape in Fig. 1;
  • Fig. 4 shows an illustration of adhesive tape drop resistance test of the stretch releasable adhesive tape in Fig. 1;
  • Fig. 5 shows comparison of stretch releasing performance of the stretch releasable adhesive tape in Fig. 1.
  • a and/or B includes, (A and B) and (A or B); “at least two” includes all numbers of two and greater (e.g., at least 4, at least 6, at least 8, at least 10, at least 25, at least 50, at least 100, etc.). “at least one” includes all numbers of one and greater (e.g., at least 2, at least 4, at least 6, at least 8, at least 10, at least 25, at least 50, at least 100, etc.).
  • cross-linking refers to connecting two pre-formed polymer chains using chemical bonds or chemical groups in order to increase the modulus of the material; “crosslinked” refers to two pre-formed polymer chains were connected using chemical bonds or chemical groups in order to increase the modulus of the material; “cross-linker” and/or “cross-linker” refers to crosslinking agents, “polymer” and “polymeric” and “polymerized product” refer to materials that are homopolymers, copolymers, terpolymers, and the like, “copolymer” and “copolymeric” refer to a polymeric material that is formed from at least two monomers. That is, a copolymer is a subset of polymers that excludes only homopolymers.
  • acrylate refers to compounds containing either an acrylate or a methacrylate structure or combinations thereof.
  • endpoints of the range are considered to be in the range.
  • the expressions “in a range from x to y”, “in a range of x to y”, “in an amount from x to y”, “in an amount of x to y”, or similar expressions include the endpoints x and y.
  • glass transition temperature refers to the temperature at which a material changes from a glassy state to a rubbery state.
  • glassy means that the material is hard and brittle (and therefore relatively easy to break) while the term “rubbery” means that the material is elastic and flexible.
  • the Tg is the critical temperature that separates their glassy and rubbery behaviors. If a polymeric material is at a temperature below its Tg, large-scale molecular motion is severely restricted because the material is essentially frozen. On the other hand, if the polymeric material is at a temperature above its Tg, molecular motion on the scale of its repeat unit takes place, allowing it to be soft or rubbery.
  • the glass transition temperature of a polymeric material is often determined using methods such as Differential Scanning Calorimetry. Any reference herein to the Tg of a monomer refers to the Tg of a homopolymer prepared from that monomer.
  • a stretch releasable adhesive tape 2 includes a release liner 4, a first layer of adhesive 6 attached to the release liner, a backing layer 8 attached to the first layer of adhesive and a second layer of adhesive 10.
  • the first layer of adhesive and second layer of adhesive may be the same.
  • the tape may include a release liner, a layer of adhesive attached to the release liner, a backing layer attached to the layer of adhesive.
  • the adhesive tape may have a minimum thickness of at least about 0.05 millimeters(mm), about 0.07 millimeters, about 0.09 millimeters, or about 1.0 millimeters, and a maximum thickness of no greater than about 1.2 millimeters.
  • 180°peel strength of the adhesive tape using ASTM D3330 testing standard is at least 0.2 N/mm, at least 0.5 N/mm, at least 0.7 N/mm, at least 0.8 N/mm, but not exceeding 1.0 N/mm.
  • backing layer 8 is made from a thermoplastic
  • the backing layer is made from a polyester based thermoplastic polyurethane polymer.
  • Suitable polyester based thermoplastic polyurethane includes but not limited to aromatic polyester based thermoplastic polyurethane, aliphatic polyester based thermoplastic polyurethane.
  • the thermoplastic polyurethane is aromatic hydroxyl terminated.
  • the weight percent of aromatic hydroxyl group is between 0.3 and 3%wt, and glass transition temperature (Tg) of soft molecular chain of the
  • thermoplastic polyurethane is between -20 to 40 ° C and glass transition
  • thermoplastic polyurethane temperature/kofler melting temperature of hard molecular chain of the thermoplastic polyurethane is between 60 tol 10 ° C .
  • thermoplastic polyurethane has tear strength above 35MPa and the shore hardness is from 55A to 70A, preferably 65 A.
  • the thermoplastic polyurethane is cross-linked by adding cross-linkers.
  • Suitable cross-linkers include isocyanate type cross-linkers.
  • the amount of isocyanate cross-linker may be from 0.1 to 0.5 weight percent, may be from 0.15 to 0.3 weight percent .
  • the the cross-linker comprises isophorondiisocyanate
  • the backing layer for the adhesive article is usually selected to have suitable mechanical properties for use in a stretch release adhesive tape.
  • the backing layer is selected so that it can be stretched (elongated) in a first direction (e.g., a lengthwise direction) at least 850 percent without breaking. That is, at least one dimension such as the length of the backing layer can be increased through stretching at least 850 percent without breaking
  • the backing layer has an elongation at break at least 850%, at least 1000%, at least 1200%, at least 1400%, at least 1600%, at least 1800%, at least 2000%), and at least 2200%).
  • the backing layer has a Young's modulus at least 25MPa, at least 30MPa, at least 35MPa, at least 45MPa, and not exceeding 50MPa.
  • the Young's Modulus can be measured, for example, using method ASTM D790-07 or ASTM D882-02.
  • the backing layer may have a thickness between 35 micron and 70 micron.
  • the backing layer may be of any suitable construction.
  • the backing layer can be in the form of a film any suitable thickness, composition, and opaqueness or clarity.
  • the backing layer can be a single layer of film, and/or multiple layers of film.
  • the adhesive layer is made of a pressure sensitive adhesive with further modification.
  • the pressure sensitive adhesive is formed from a reaction mixture which includes below components:
  • polyurethane polymer based on a total weight of the reaction mixture; 0 weight percent to 45 weight percent of tackifier based on a total weight of the reaction mixture, 0.02 weight percent to 0.1 weight percent of cross-linker based on a total weight of the reaction mixture; and
  • Suitable acrylic copolymer is described in US Pub. No. 20110104486A1 which is hereby incorporated by reference.
  • the weight percent of the acrylic copolymer may be from 25 to 90, from 30 to 90, from 40 to 80, from 50 to 70, from 60 to 65 weight percent, based on a total weight of the reaction mixture.
  • the acrylic copolymer includes 3 weight percent to 10 weight percent of acrylic acid monomer based on a total weight of the acrylic copolymer.
  • the functional group terminated polyurethane polymer includes aliphatic sulfonic acid terminated polyurethane, or aromatic hydroxyl terminated polyurethane, or their combinations.
  • the Tg of the functional group terminated polyurethane is between 60 and 80 ° C .
  • the weight percent of the functional group terminated polyurethane varies from 5 to 30, varies from 10 to 25, varies from 10 to 15, based on a total weight of the reaction mixture.
  • functional group terminated polyurethane polymer includes aliphatic sulfonic acid terminated polyurethane and the weight percent of sulfonic acid group is between 2 and 5%.
  • the tackifier used in the present invention includes but not limited to rosin resins, terpene resins.
  • the weight percent of the tackifier varies from 0 to 45, varies from 4-45, varies from 10-35, varies from 15 to 30, varies from 20 to 30, based on a total weight of the reaction mixture.
  • the cross-linker used in the present invention includes but not limited to polyisocynate.
  • the amount of the cross-linker varies from 0.02 to 0.1, 0.05 to 0.09, 0.06 to 0.08 weight percent based on a total weight of the reaction mixture.
  • the NCO (isocyanate group) content of the cross-linker is from 5 to 12% and the viscosity of cross-linker is from 400 to 800cP.
  • Suitable cross-linker includes but not limited to aliphatic polyisocyanate (IPDI trimer, HDI trimer).
  • the reaction mixture may include 0-3 weight percent of pigment if it is desired to change the color of the adhesive tape.
  • T-peel was performed according to ASTM D1876 using an an Instron
  • Stretch releasing test was performed on a sample of 90mmx20mmx0.1mm (thickness) using an Instron (model 4465) at cross head speed of 12 inch/min and at 90 degree pulling angle as shown in Fig.3. Reliability of stretch-release was recorded as a percentage of clean removal samples over total samples tested. The stretch releasing test was performed on 1) the original sample and 2) the sample after aging at 65 ° Cand RH95% for 72hrs.
  • Drop resistance test was performed on a sample of 60mmx20mm as shown in Fig.4.
  • the testing device includes a plate 14, a support 16 connected with the plate, and testing blocks 18, and a base 20 used to support the testing blocks via a rod with a certain height.
  • an article with the present invention of tape is dropped from the surface of the plate to test its drop resistance with adhered to the testing blocks 18.
  • Drop height was increased at 5 cm increment from the initial height and the height of failure (HOFF) was observed. Any partial adhesive failure/peeling was counted as failure.
  • the residue on a substrate which the adhesive is removed from is measured by visibility, i.e. by eyes.
  • Stretch releasing test was performed on a sample of 90mmx20mmx0.1mm (thickness) using an Instron (model 4465) at cross head speed of 12 inch/min and at 90 degree pulling angle as shown in Fig.3. Reliability of stretch-release was recorded as a percentage of clean removal samples over total samples tested. The stretch releasing test was performed on 1) the original sample and 2) the sample after aging at 65 ° Cand RH95% for 72hrs.
  • Adhesive solution with 40% solids was prepared by mixing the components (except cross-linker) as listed in Tab.2 under Modified Acrylic Adhesive to yield a coatable solution having a viscosity of about 8,000cps.
  • the adhesive solution is then mixed with DESMODUR DN cross-linker and coated on a polyolefin coated Kraft (PCK) release liner using a solvent coater and dried in a continuous heating oven at 105 °C for 2 minutes to yield a 21 micrometer adhesive layer.
  • PCK polyolefin coated Kraft
  • Polyurethane solution was prepared by first mixing 25 parts aromatic polyester-based thermoplastic polyurethane (ESTANE 5702) with 75 parts methylethylketone (MEK) and then introducing Z4470 cross-linker.
  • the PU solution was coated on a PCK liner using a solvent coater and dried in a continuous heating oven at 80 °C for 5 minutes to yield a 58 micrometer thickness of PU layer.
  • the multilayer adhesive tape of this invention is prepared by laminating adhesive skin layer to both surfaces of PU layer as shown in Fig 1. Such adhesives may be coated onto the backing layer 8 to form the adhesive tape 2, or such adhesives may be used to form an adhesive article in the form of a single homogeneous layer of adhesive (i.e. without a backing layer).
  • the construction of the stretch releasable tape includes the polyolefin coated KRAFT (PCK) release liner, first layer of modified acrylic adhesive, specific polyurethane core and second layer of modified acrylic adhesive just as shown in Fig.1.
  • the formulation of 1 st layer and 2nd layer of modified acrylic adhesive may be the same.
  • a hot melt process is also suitable to prepare the stretch release tape by extruder and multi-layer co-extrusion die to form the adhesive layer and core layer.
  • Comparative examples are shown in Tab.2. Comparatives CI (T company 0.1mm Bond & Detach DC tape) and C2 (M company 0.9mm) are commercial products as described in Table 2. Comparatives C3 & C4 were prepared using the same procedure described in El & E2 except the adhesive contains no thermoplastic PU addition as shown in Table 2.
  • Tab. 3 shows construction of the stretch-releasable adhesive tapes of the present invention in comparison with the competitive tapes.
  • comparatives CI and C2 show poor releasing reliability: 70% for CI and 0% for C2 as these are conventional stretch-releasable tapes originally designed for in-plane stretch-release.
  • the adhesive tape of the present invention examples El & E2 comprising a modified acrylic adhesive with aliphatic sulfonic acid terminated polyurethane, i.e. SINOCHEM and crosslinked aromatic hydroxyl terminated polyurethane, show >1000% elongation at break and >40 MPa maximums stress. Comparing the testing results of El vs. C3 and E2 vs.
  • Fig. 5 shows the vertical stretch-release performance of El, CI and C2 where CI and C2 have significantly lower elongation at break and maximum stress compared to El .
  • C2 shows noticeably reduced elongation at break and tensile while E2 maintains high elongation at break and tensile strength.
  • composition as invented not only has advantages in balanced adhesion, vertical stretch-release performance and drop resistance, but also has improved heat-humidity aging resistance over the completive tapes on the market.

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

Abstract

L'invention concerne un ruban adhésif pouvant être enlevé par étirement, comprenant un envers et une première couche d'une composition adhésive sensible à la pression, appliquée sur au moins une surface dudit envers, le ruban adhésif ayant une épaisseur comprise entre 0,05 et 0,10 mm et un allongement à la rupture compris entre 850 % et 2200 %, capable d'être fermement collé à un substrat, et pouvant ensuite en être enlevé après avoir été étiré à un angle de 90° ou plus par rapport à la surface d'un substrat, sans se rompre avant que le ruban ne soit enlevé du substrat, et sans laisser sur le substrat une quantité importante du résidu de l'adhésif sensible à la pression, l'adhésif sensible à la pression contenant un polyuréthanne terminé par un groupe fonctionnel. Un dispositif électronique est aussi décrit, comprenant un ruban adhésif pouvant être enlevé par étirement selon l'invention.
EP14885414.4A 2014-03-11 2014-03-11 Article adhésif pouvant être enlevé par étirement, utilisation et fabrication de cet article Withdrawn EP3116964A4 (fr)

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CN105524570B (zh) * 2016-01-18 2018-10-12 3M创新有限公司 胶带组件、粘结制品
JP6704783B2 (ja) * 2016-04-28 2020-06-03 日東電工株式会社 粘着シート
CN107674602B (zh) * 2016-08-02 2020-07-10 滕超 一种可拉伸移除的胶粘带及其制备方法
EP3625827B1 (fr) * 2017-05-15 2024-05-08 Carestream Health, Inc. Module de substrat flexible et procédé de fabrication
JP7094148B2 (ja) * 2017-10-02 2022-07-01 日東電工株式会社 粘着テープ
WO2019069541A1 (fr) * 2017-10-02 2019-04-11 日東電工株式会社 Ruban auto-adhésif
US20220024119A1 (en) * 2018-12-06 2022-01-27 Jabil Inc. Apparatus, system and method of additive manufacturing to impart specified characteristics to the print material and the printed output
KR102530957B1 (ko) * 2020-08-19 2023-05-09 테사 소시에타스 유로파에아 폴리우레탄 캐리어를 갖는 접착 테이프
DE102020210505A1 (de) 2020-08-19 2022-02-24 Tesa Se Klebeband mit Polyurethanträger
DE102020210503B4 (de) 2020-08-19 2023-10-26 Tesa Se Klebeband mit Polyurethanträger, Verfahren zur Herstellung und Verwendung
DE102021210261A1 (de) 2021-09-16 2023-03-16 Tesa Se Klebeband mit vernetztem Polyurethanträger
DE102022131231A1 (de) 2022-10-14 2024-04-25 Tesa Se Wiederablösbares Haftklebeband

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US4287013A (en) * 1979-05-08 1981-09-01 Minnesota Mining & Manufacturing Company Comformable, multilayered tape adherent on one surface to fusable metal alloys and on the other surface to ophthalmic lens blanks
JP4493643B2 (ja) * 2006-12-06 2010-06-30 日東電工株式会社 再剥離型粘着剤組成物、及び粘着テープ又はシート
JP5572487B2 (ja) * 2010-09-01 2014-08-13 日東電工株式会社 粘弾性体及びその製造方法
CN102602097B (zh) * 2012-03-07 2015-12-09 深圳星立东科技有限公司 一种聚氨酯保护膜
WO2013148506A1 (fr) * 2012-03-30 2013-10-03 3M Innovative Properties Company Mélanges adhésifs autocollants à base d'urée et à base d'uréthane
CN202705294U (zh) * 2012-07-16 2013-01-30 斯迪克新型材料（江苏）有限公司 压敏双面胶带

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