WO2013129462A1 - Ruban adhésif - Google Patents

Ruban adhésif Download PDF

Info

Publication number
WO2013129462A1
WO2013129462A1 PCT/JP2013/055103 JP2013055103W WO2013129462A1 WO 2013129462 A1 WO2013129462 A1 WO 2013129462A1 JP 2013055103 W JP2013055103 W JP 2013055103W WO 2013129462 A1 WO2013129462 A1 WO 2013129462A1
Authority
WO
WIPO (PCT)
Prior art keywords
fatty acid
pressure
sensitive adhesive
acid amide
adhesive tape
Prior art date
Application number
PCT/JP2013/055103
Other languages
English (en)
Japanese (ja)
Inventor
俊隆 鈴木
石黒　繁樹
拓三 由藤
洋毅 千田
真理 松本
裕香 関口
あや 長友
文輝 浅井
敏正 杉村
白井　稚人
Original Assignee
日東電工株式会社
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 日東電工株式会社 filed Critical 日東電工株式会社
Priority to CN201380007921.4A priority Critical patent/CN104093804A/zh
Publication of WO2013129462A1 publication Critical patent/WO2013129462A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/20—Adhesives in the form of films or foils characterised by their carriers
    • C09J7/22—Plastics; Metallised plastics
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/20—Carboxylic acid amides
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00—Additional features of adhesives in the form of films or foils
    • C09J2301/10—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
    • C09J2301/12—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers
    • C09J2301/122—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers the adhesive layer being present only on one side of the carrier, e.g. single-sided adhesive tape
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00—Additional features of adhesives in the form of films or foils
    • C09J2301/40—Additional features of adhesives in the form of films or foils characterized by the presence of essential components
    • C09J2301/408—Additional features of adhesives in the form of films or foils characterized by the presence of essential components additives as essential feature of the adhesive layer
    • 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
    • C09J2301/41—Additional features of adhesives in the form of films or foils characterized by the presence of essential components additives as essential feature of the carrier layer
    • 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
    • C09J2427/00—Presence of halogenated polymer
    • C09J2427/006—Presence of halogenated polymer in the substrate
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2433/00—Presence of (meth)acrylic polymer

Definitions

  • the present invention relates to an adhesive tape.
  • a PVC film or the like has been used as a base layer of an adhesive tape that can be re-peeled in a semiconductor manufacturing process or the like.
  • the pressure-sensitive adhesive tape is constituted by applying a pressure-sensitive adhesive layer on one surface of a base material layer made of such a PVC film, and a fatty acid amide is added to the base material or pressure-sensitive adhesive (Japanese Patent Laid-Open No. 57-139163).
  • the unwinding property and the adhesion to the adherend are controlled by appropriately bleeding the fatty acid amide on the pressure-sensitive adhesive surface.
  • It has also been proposed to obtain good peelability and stain resistance by adding a urea compound and hydrotalcite to a vinyl chloride resin Japanese Patent Laid-Open No. 07-276516).
  • the adhesive property is not stable, and the adherend to the adherend such as a semiconductor wafer when the adhesive tape is peeled off is large.
  • the adhesive tape is peeled off from the adherend due to the storage state of the adhesive tape, the storage state after bonding to the adherend, etc., it becomes difficult to peel off or contaminants such as an adhesive remain on the adherend. Etc. may occur.
  • the present invention has been made in view of the above problems, and can provide a stable adhesive property and peeling property even under various environments, and can minimize contamination on an adherend.
  • the purpose is to provide.
  • the present inventors have found that methylene bis-fatty acid amide contained as an additive in the base material layer or pressure-sensitive adhesive layer of the pressure-sensitive adhesive tape.
  • the present inventors have found that there are many impurities derived from raw materials and by-products during synthesis, and that the amount of impurities in the commercial product has a large variation for each production lot. Therefore, by removing impurities of methylene bis fatty acid amide and adding it to the base material layer or pressure sensitive adhesive layer of the pressure sensitive adhesive tape, it is possible to unexpectedly stabilize the adhesive properties and to adhere to the adherend when peeled. It has been found that contamination can be significantly reduced.
  • the fatty acid generated during the formation of methylene bis fatty acid amide effectively increases the time-dependent increase in adhesive strength after bonding of the adhesive tape to the adherend. It was newly found that it can be suppressed.
  • the balance of storage of adhesive tape and pasting to adherend has been balanced and stabilized.
  • the pressure-sensitive adhesive tape of the present invention capable of obtaining adhesive properties and peeling properties has been completed.
  • the adhesive tape of the present invention is A pressure-sensitive adhesive tape in which a pressure-sensitive adhesive layer is formed on one side of a thermoplastic resin film, and at least one of the thermoplastic resin film and the pressure-sensitive adhesive layer contains methylene bis fatty acid amide and a fatty acid, Fatty acid monoamide, which is a by-product during the production of methylene bis fatty acid amide, is substantially not contained.
  • Such an adhesive tape preferably includes one or more of the following.
  • the methylene bis fatty acid amide is obtained by removing the fatty acid monoamide as the by-product by solvent extraction.
  • Methylene bis fatty acid amide is a compound represented by the formula (I).
  • R 1 —Am—CH 2 —Am—R 2 (I) (In the formula, R 1 and R 2 each independently represents a saturated or unsaturated hydrocarbon group having 6 to 23 carbon atoms, and Am represents a secondary amide group.)
  • the fatty acid is contained in the range of 0.1 to 30 parts by weight with respect to 100 parts by weight of methylene bis fatty acid amide.
  • Methylene bis fatty acid amide and fatty acid are each contained in the range of 0.1 to 5.0 parts by weight with respect to 100 parts by weight of the thermoplastic resin.
  • the thermoplastic resin film is a film made of soft polyvinyl chloride containing a plasticizer.
  • the pressure-sensitive adhesive layer contains an acrylic polymer as a base polymer.
  • a release liner is disposed on the pressure-sensitive adhesive layer side of the adhesive tape.
  • the pressure-sensitive adhesive tape of the present invention it is possible to obtain stable adhesive properties and peeling properties under various environments, and to minimize contamination on the adherend.
  • the pressure-sensitive adhesive tape of the present invention is mainly formed by a thermoplastic resin film as a base material layer and a pressure-sensitive pressure-sensitive adhesive layer laminated on one surface of the thermoplastic resin film.
  • Either one of the thermoplastic resin film and the pressure-sensitive adhesive layer contains methylene bis fatty acid amide and a fatty acid. These layers are substantially free of fatty acid monoamide.
  • the methylene bis fatty acid amide and the fatty acid may be contained only in the thermoplastic resin film or the pressure sensitive adhesive layer, either one is contained in the pressure sensitive adhesive layer, and the other is contained in the thermoplastic resin film.
  • thermoplastic resin film may be contained in the pressure-sensitive adhesive layer, the other may be contained in both the pressure-sensitive adhesive layer and the thermoplastic resin film, or one of them may be contained in the thermoplastic resin film and the other is sensitive. It may be contained in both the pressure-sensitive adhesive layer and the thermoplastic resin film, or may be contained in both the thermoplastic resin film and the pressure-sensitive adhesive layer. As will be described later, when the thermoplastic resin film and / or the pressure-sensitive adhesive layer has a laminated structure, it may be contained in one of them, but at least the thermoplastic resin film and the pressure-sensitive adhesive layer Are preferably contained in layers in contact with each other.
  • the pressure-sensitive adhesive tape of the present invention is suitably provided with a release liner in contact with the pressure-sensitive pressure-sensitive adhesive layer as necessary.
  • the methylene bis fatty acid amide in the present invention can be represented by, for example, the formula (I).
  • R 1 —Am—CH 2 —Am—R 2 (I) (In the formula, R 1 and R 2 each independently represents a saturated or unsaturated hydrocarbon group having 6 to 23 carbon atoms, and Am represents a secondary amide group.)
  • Examples of the compound represented by the formula (I) include compounds represented by the formula (II) or the formula (III). (In the formula, R 1 and R 2 each independently represents a saturated or unsaturated hydrocarbon group having 6 to 23 carbon atoms.)
  • This methylene bis fatty acid amide may be contained alone or in combination of two or more. More specifically, the compounds represented by the formula (II) and the formula (III) may each be one kind, a mixture of two or more kinds, or the formula (II) It may be a mixture of the compound represented by the formula (III). In the formulas (I) to (III), R 1 and R 2 may be different from each other but are preferably the same. Of these, the compound represented by the formula (II) is preferable. Furthermore, as the compound represented by the formula (II), a compound represented by the formula (IV) is more preferable. CH 3 — (CH 2 ) n —CO—NH—CH 2 —NH—CO— (CH 2 ) m —CH 3 (IV) (In the formula, n and m each independently represents an integer of 5 to 22.)
  • the saturated or unsaturated hydrocarbon group includes any of linear, branched, cyclic, and combinations thereof.
  • Saturated hydrocarbon groups include methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, t-butyl, pentyl, hexyl, heptyl, octyl, decyl, dodecyl
  • a chain alkyl group such as a group, tetradecyl group, hexadecyl group, octadecyl group; Branched alkyl groups such as ethylhexyl, ethyloctyl, propylhexyl; Examples thereof include cyclic alkyl groups such as a cyclopentyl group, a cyclohexyl group, and a cycloheptyl group.
  • Examples of the unsaturated hydrocarbon group include alkenyl groups such as propenyl group, isopropenyl group, 2-propenyl group, 9-octadecynyl group, cyclopentenyl group, and cyclohexenyl group, and cycloalkenyl groups.
  • the carbon number is preferably 8 to 20, and more preferably 10 to 18. Saturated hydrocarbons are preferred.
  • n and m preferably have 7 to 19 carbon atoms, more preferably 9 to 17 carbon atoms, and still more preferably 11 to 17 or 13 to 15 carbon atoms.
  • the secondary amide group in formula (I) means a divalent amide group, and the carbon atom in the amide group may be bonded to either R 1 or R 2 and a methylene group.
  • Specific compounds of formula (II) include N, N′-methylenebiscapric amide, N, N′-methylenebislauric acid amide, N, N′-methylenebismyristic acid amide, N, N′-methylenebispalmitic acid amide, N, N′-methylenebisoleic acid amide, N, N′-methylenebisstearic acid amide, N, N′-methylenebisbehenamide, N, N′-methylenebiserucic acid amide and the like can be mentioned.
  • Specific compounds of formula (III) include N, N′-dicaprylmalonic acid amide, N, N′-dilarylmalonic acid amide, N, N′-dimyristylmalonic acid amide, N, N′-dipalmitylmalonic acid amide, N, N′-dioleoylmalonic acid amide, N, N′-distearylmalonic acid amide, N, N′-dibehenylmalonic acid amide, N, N′-diercarylmalonic acid amide and the like can be mentioned.
  • N, N′-methylenebisstearic acid amide, N, N′-methylenebispalmitic acid amide and combinations thereof are preferable, and N, N′-methylenebisstearic acid amide and N, N′-methylene bisamide are preferable. More preferred is a mixture of palmitic amides.
  • methylene bis fatty acid amide is produced by the reaction of fatty acid amide and formaldehyde as shown below. Moreover, fatty acid amide is industrially produced
  • methylene bis fatty acid amide obtained by the reaction of fatty acid amide and formaldehyde and having a very high purity by the purification can exist, but in reality, as an industrial product, impurities are substantially reduced. There is no methylene bis fatty acid amide not present.
  • the methylene bis fatty acid amide itself is contained with high purity, so that the intended characteristics can be exhibited and unintended effects can be suppressed. Therefore, the methylene bis fatty acid amide obtained by the reaction of the fatty acid amide and formaldehyde is preferably purified by being subjected to extraction with a predetermined solvent (including washing).
  • a predetermined solvent including washing.
  • the solvent it is suitable to use a solvent that dissolves the mono-fatty acid amide used as a raw material but does not dissolve the methylene bis-fatty acid amide.
  • dissolving means that the amount of solvent necessary for dissolving 1 g of solute is 10 g or less, and not dissolving means that the amount of solvent necessary for dissolving 1 g of solute is 100 g or more.
  • this solvent chloroform, ethanol, methanol, these heating solvents, etc. are mentioned. Of these, chloroform, heated ethanol, heated methanol and the like are preferable.
  • Any known method can be used for extraction. Examples thereof include a method in which methylene bis fatty acid amide obtained by the reaction of fatty acid monoamide and formaldehyde is immersed in a solvent for washing, and a method in which the obtained methylene bis fatty acid amide is subjected to Soxhlet extraction using a solvent.
  • the conditions at this time are not particularly limited. For example, a solvent having a volume of about 30 to 100 times or a weight of methylene bis fatty acid amide is added, and immersion, immersion, washing or extraction is performed for about 30 minutes to several hours. Do. Depending on the type of solvent used, the solvent may be heated to room temperature to about 100 ° C. Further, if necessary, such an operation may be repeated a plurality of times by changing the solvent type or using the same type of solvent. The obtained insoluble matter is separated by a known means such as filtration.
  • drying can utilize any method commonly performed in the art.
  • the drying conditions and temperature are not particularly limited and are preferably adjusted as appropriate.
  • 40 ml of chloroform is added to about 1 g of commercially available methylene bis-fatty acid amide, soaked for 1 hour using a soaking machine, and then insoluble and soluble components by suction filtration.
  • the purified methylenebis fatty acid amide composition can be obtained by performing the same operation about the obtained chloroform-insoluble matter about twice more.
  • ethanol extraction for example, 40 ml of ethanol is added to about 1 g of commercially available methylene bis fatty acid amide, and the mixture is extracted by heating at 80 ° C. (hot plate temperature) for 1 hour. Then, it isolate
  • methylene bis fatty acid amide used in the present invention is substantially free from fatty acid monoamides.
  • fatty acid monoamide preferably fatty acid
  • it is less than 0.5% by weight, preferably Less than 0.4 wt%, less than 0.25 wt%, less than 0.2 wt%, less than 0.1 wt%, 0.05 wt%, measured below the detection limit, or contained in multiple species
  • the total amount is less than 2% by weight, preferably less than 1.6% by weight, less than 1% by weight, less than 0.8% by weight, less than 0.5% by weight, less than 0.4% by weight, 0.3% It is preferably less than wt%, 0.05 wt%, and below the detection limit.
  • the fatty acid monoamide that is not substantially contained (removed) is not only a by-product that is produced during the production of methylene bis-fatty acid amide, but is also produced at least as a by-product after the production. It means that the fatty acid monoamide of the same kind, preferably, a different kind of fatty acid monoamide is not contained.
  • the methylene bis fatty acid amide used in the present invention is a fatty acid monoamide derived from the raw material / production method or the like / different fatty acid monoamides such as lauric acid monoamide, stearic acid monoamide, oleic acid monoamide, erucic acid monoamide, capric acid.
  • the methylene bis fatty acid amide used in the present invention is a fatty acid derived from the raw material or the like or a fatty acid of the same or different type, such as capric acid, stearic acid, oleic acid, erucic acid, lauric acid, palmitic acid, myristic acid, It is preferable that behenic acid and the like, especially stearic acid, oleic acid, palmitic acid and the like are not contained, and it is more preferable that stearic acid and palmitic acid and the like are not contained. Alternatively, even if the methylene bis fatty acid amide contains a fatty acid derived from a raw material or the like, it is suitable to measure the content by analysis or the like.
  • either one of the thermoplastic resin film and the pressure-sensitive adhesive layer contains a fatty acid with a specific content.
  • the fatty acid in this case may be the same type of fatty acid as that constituting the methylene bis fatty acid amide, may be a different fatty acid, or a mixture of two or more of these. That is, the fatty acid is contained in at least one of the thermoplastic resin film and the pressure-sensitive pressure-sensitive adhesive layer, but the total amount is a combination of each component when producing the thermoplastic resin film or the pressure-sensitive pressure-sensitive adhesive layer. It is suitable to be controlled at times.
  • the methylene bis fatty acid amide used in the present invention is substantially free of fatty acid amide (preferably substantially free of fatty acid).
  • a minor component such as an amide tris may be contained. It is preferable that such a tris body is not substantially contained.
  • the amount of methylenebisfatty acid amide and fatty acid added to the thermoplastic resin film is, for example, about 0.1 to 5.0 parts by weight with respect to 100 parts by weight of the thermoplastic resin in the thermoplastic resin film, respectively.
  • the range is preferably about 0.1 to 3.0 parts by weight.
  • the amount of methylene bis fatty acid amide and fatty acid added in the pressure-sensitive adhesive layer is, for example, preferably in the range of about 0.1 to 5.0 parts by weight with respect to 100 parts by weight of the base polymer described later, More preferably, it is about 0.1 to 3.0 parts by weight.
  • the total amount added is 0.1 to 5.0 with respect to 100 parts by weight of the thermoplastic resin. It is preferable to adjust appropriately in the range of about parts by weight, and more preferably about 0.1 to 3.0 parts by weight.
  • the fatty acid is suitably contained in a range of about 0.1 to 30 parts by weight with respect to 100 parts by weight of methylenebisfatty acid amide, about 0.1 to 20 parts by weight, It is preferably contained in the range of about 0.1 to 10 parts by weight and about 0.1 to 5 parts by weight.
  • the content described above means the total amount in each layer constituting the adhesive tape.
  • thermoplastic resin film of the present invention is not particularly limited, and for example, low density polyethylene, linear polyethylene, medium density polyethylene, high density polyethylene, ultra low density polyethylene, random copolymer polypropylene, block copolymer polypropylene, homopolypropylene.
  • Polyolefins such as polybutene and polymethylpentene; ethylene-vinyl acetate copolymer, ionomer resin, ethylene- (meth) acrylic acid copolymer, ethylene- (meth) acrylic acid ester (random, alternating) copolymer, ethylene -Polyolefin resins such as butene copolymer and ethylene-hexene copolymer; Polyester resins such as polyurethane, polyethylene terephthalate, and polyethylene naphthalate; (Meth) acrylic polymers, polystyrene, polycarbonate Polyimide, polyamide, polyamideimide, polyetherimide, polysulfone, polyether sulfone, polyvinyl chloride, polyvinylidene chloride, fluorine resins, films made of cellulose resins and thermoplastic resins such as a cross-linked product thereof. These thermoplastic resins may be used by blending several kinds as required. Of these, a vinyl
  • the vinyl chloride resin includes polyvinyl chloride, a vinyl chloride copolymer, a graft copolymer onto polyvinyl chloride, and a mixture with other resins.
  • the comonomer in the vinyl chloride copolymer include vinyl esters such as vinyl acetate, vinyl ethers such as ethylene vinyl ether, ⁇ -olefins such as ethylene, propylene, and 1-butene, methyl acrylate, (Meth) acrylic acid esters such as ethyl acrylate, methyl methacrylate and butyl methacrylate, vinylidene chloride and the like.
  • a soft vinyl chloride resin to which a plasticizer described later is added is preferable.
  • the thermoplastic resin film preferably contains a plasticizer so that the pressure-sensitive adhesive tape obtained from the thermoplastic resin film exhibits appropriate flexibility. Further, if necessary, a stabilizer, a filler lubricant, a colorant, and an ultraviolet absorber. An additive such as an agent and an antioxidant may be included.
  • the plasticizer is not particularly limited. For example, phthalate ester-based, trimellitic acid ester-based (Dainippon Ink Co., Ltd.
  • an ester plasticizer You may use these individually or in combination of 2 or more types.
  • the plasticizer is suitably used in a proportion of, for example, 10 to 60 parts by weight with respect to 100 parts by weight of the thermoplastic resin, and preferably 10 to 30 parts by weight.
  • the stabilizer is not particularly limited, and examples thereof include composite stabilizers such as barium-zinc, tin, calcium-zinc, cadmium-barium.
  • the filler include inorganic fillers such as calcium carbonate, silica and mica, and metal fillers such as iron and lead.
  • the colorant include pigments and dyes. Any other additive known in the art can be used.
  • the thermoplastic resin film may be a single-layer film, or may be a laminate of films (multilayer film) that is different in material or composition and takes advantage of each resin.
  • the thickness of the thermoplastic resin film can be adjusted according to the physical properties of the adhesive tape to be obtained. For example, the thickness is 30 to 1000 ⁇ m, preferably 40 to 800 ⁇ m, more preferably 50 to 500 ⁇ m, and particularly preferably 60 to 200 ⁇ m. Can be mentioned.
  • a conventional surface treatment such as corona treatment, chromic acid treatment, Oxidation by a chemical or physical method such as ozone exposure, flame exposure, high-voltage impact exposure, or ionizing radiation treatment may be performed.
  • the pressure-sensitive adhesive (hereinafter sometimes simply referred to as “adhesive”) layer is formed of a pressure-sensitive adhesive.
  • the pressure sensitive adhesive is not particularly limited. For example, depending on the type of base polymer constituting the adhesive, a rubber adhesive, an acrylic adhesive, a polyamide adhesive, a silicone adhesive, and a polyester adhesive. Although an adhesive, a urethane type adhesive, etc. are mentioned, It can select suitably from these well-known adhesives. Among these, acrylic pressure-sensitive adhesives are excellent in various properties such as heat resistance and weather resistance, and can exhibit desired properties by selecting the types of monomer components constituting the acrylic polymer. Can be preferably used.
  • the acrylic pressure-sensitive adhesive is usually formed of a base polymer composed mainly of an acrylic polymer such as (meth) acrylic acid alkyl ester.
  • the (meth) acrylic acid alkyl ester include, for example, methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, isopropyl (meth) acrylate, butyl (meth) acrylate, (meth) Isobutyl acrylate, sec-butyl (meth) acrylate, t-butyl (meth) acrylate, pentyl (meth) acrylate, hexyl (meth) acrylate, heptyl (meth) acrylate, octyl (meth) acrylate, 2-Methylhexyl acrylate, isooctyl (meth) acrylate, nonyl (meth) acrylate, isononyl (meth
  • Acrylic polymers contain units corresponding to other monomer components copolymerizable with (meth) acrylic acid alkyl esters as necessary for the purpose of modifying cohesive strength, heat resistance, crosslinkability and the like. You may go out.
  • a monomer component for example, Carboxyl group-containing monomers such as acrylic acid, methacrylic acid, carboxyethyl acrylate, carboxypentyl acrylate, itaconic acid, maleic acid, fumaric acid, crotonic acid; Hydroxybutyl (meth) acrylate, hydroxyhexyl (meth) acrylate, hydroxyoctyl (meth) acrylate, hydroxydecyl (meth) acrylate, hydroxylauryl (meth) acrylate, (4-hydroxymethylcyclohexyl) methyl methacrylate, etc.
  • Carboxyl group-containing monomers such as acrylic acid, methacrylic acid, carboxyethyl acrylate, carboxypentyl
  • a hydroxyl group-containing monomer of Sulphonic acid groups such as styrene sulfonic acid, allyl sulfonic acid, 2- (meth) acrylamide-2-methylpropane sulfonic acid, (meth) acrylamide propane sulfonic acid, sulfopropyl (meth) acrylate, (meth) acryloyloxynaphthalene sulfonic acid Containing monomers;
  • Phosphoric acid group-containing monomers such as 2-hydroxyethyl acroyl phosphate, (meth) acrylamide, N, N-dimethyl (meth) acrylamide, N-butyl (meth) acrylamide, N-methylol (meth) acrylamide, N-methylolpropane (N-substituted) amide monomers such as (meth) acrylamide; Aminoalkyl (meth) acrylate monomers such as aminoethyl (meth) acrylate, N, N-dimethylaminoethyl (meth) acrylate, and t-butylaminoethyl (meth) acrylate; (Meth) acrylic acid alkoxyalkyl monomers; Maleimide monomers such as N-cyclohexylmaleimide, N-isopropylmaleimide, N-laurylmaleimide, N-phenylmaleimide; Itaconimide monomers such as N-
  • Succinimide monomers such as N- (meth) acryloyloxymethylenesuccinimide, N- (meth) acryloyl-6-oxyhexamethylenesuccinimide, N- (meth) acryloyl-8-oxyoctamethylenesuccinimide; Vinyl acetate, vinyl propionate, N-vinyl pyrrolidone, methyl vinyl pyrrolidone, vinyl pyridine, vinyl piperidone, vinyl pyrimidine, vinyl piperazine, vinyl pyrazine, vinyl pyrrole, vinyl imidazole, vinyl oxazole, vinyl morpholine, N-vinyl carboxylic acid amides, Vinyl monomers such as styrene, ⁇ -methylstyrene, N-vinylcaprolactam;
  • Cyanoacrylate monomers such as acrylonitrile and methacrylonitrile; Epoxy group-containing acrylic monomers such as (meth) glycidyl acrylate; Glycol-based acrylic ester monomers such as (meth) acrylic acid polypropylene glycol, (meth) acrylic acid methoxyethyl glycol, (meth) acrylic acid methoxypolypropylene glycol; Acrylic acid ester monomers having a heterocyclic ring such as tetrahydrofurfuryl (meth) acrylate, fluorine (meth) acrylate, silicone (meth) acrylate, halogen atoms, silicon atoms, etc .;
  • Polyfunctional monomers such as acrylate, pentaerythritol tri (meth) acrylate, dipentaerythritol hexa (meth) acrylate, epoxy acrylate, polyester acrylate, urethane acrylate, divinylbenzene, butyl di (meth) acrylate, hexyl di (meth) acrylate; Olefin monomers such as isoprene, dibutadiene, isobutylene; And vinyl ether monomers such as vinyl ether. These monomer components can be used alone or in combination of two or more.
  • the acrylic copolymer can be produced by subjecting the above (meth) acrylic acid alkyl ester and, if necessary, other monomers to polymerization by a known appropriate method.
  • the molecular weight of the acrylic copolymer is not particularly limited, and for example, those having a weight average molecular weight of 100,000 to 2,000,000, preferably 150,000 to 1,000,000, more preferably 300,000 to 1,000,000 can be used.
  • the weight average molecular weight can be a value measured, for example, by gel permeation chromatography (GPC) using polystyrene as a molecular weight standard substance.
  • the pressure sensitive adhesive can be made into an energy ray curable pressure sensitive adhesive by adding an energy ray polymerizable compound or introducing an energy ray polymerizable double bond into the base polymer.
  • the pressure-sensitive adhesive layer using the energy ray-curable pressure-sensitive adhesive exhibits a sufficient adhesive force with the adherend before irradiation with the energy beam, but the adhesive strength significantly decreases after the irradiation with the energy ray, and is applied to the adherend. It can be easily peeled off without applying stress and without residual adhesive.
  • energy rays include ultraviolet rays and electron beams.
  • the energy beam polymerizable compound a compound having two or more energy beam polymerizable carbon-carbon double bonds in the molecule can be used.
  • examples of such compounds include polyfunctional acrylate compounds.
  • polyfunctional acrylate compounds include 1,4-butylene di (meth) acrylate, 1,5-pentanediol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, and 1,9-nonanediol.
  • (Meth) acrylates of linear aliphatic polyols such as di (meth) acrylate, polyethylene glycol di (meth) acrylate, polypropylene glycol di (meth) acrylate;
  • (Meth) acrylates of branched aliphatic polyols such as trimethylolpropane tri (meth) acrylate, pentaerythritol tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, and their condensates (ditrimethylolpropane tetraacrylate, And dipentaerythritol hexaacrylate). You may use these individually or in combination of 2 or more types.
  • a polyfunctional acrylate oligomer such as a urethane acrylate oligomer may be used.
  • the urethane acrylate oligomer is obtained, for example, by reacting a urethane oligomer obtained by the reaction of a diisocyanate compound and a polyol compound with a (meth) acrylic acid alkyl ester having a hydroxyl group.
  • diisocyanate compound examples include tolylene diisocyanate, diphenylmethane diisocyanate, hexamethylene diisocyanate, phenylene diisocyanate, dicyclohexylmethane diisocyanate, xylene diisocyanate, tetramethylxylene diisocyanate, naphthalene diisocyanate, and isophorone diisocyanate.
  • polyol compounds include ethylene glycol, 1,4-butanediol, 1,6-hexanediol, diethylene glycol, trimethylolpropane, dipropylene glycol, polyethylene glycol, polypropylene glycol, pentaerythritol, dipentaerythritol, and glycerin.
  • Polyester polyol compound obtained by condensation reaction of alcohols, polyhydric alcohols and aliphatic dicarboxylic acids such as adipic acid, sebacic acid, azelaic acid, maleic acid or aromatic dicarboxylic acids such as terephthalic acid and isophthalic acid ;
  • Polyether polyol compounds such as polyethylene ether glycol, polypropylene ether glycol, polytetramethylene ether glycol, polyhexamethylene ether glycol; Lactone polyol compounds such as polycaprolactone glycol, polypropiolactone glycol, polyvalerolactone glycol; Examples thereof include polycarbonate polyol compounds obtained by dealcoholization reaction of polyhydric alcohols such as ethylene glycol, propylene glycol, butanediol, pentanediol, octanediol, and nonanediol with diethylene carbonate, dipropylene carbonate and the like.
  • hydroxyl group-containing (meth) acrylic acid alkyl ester compounds examples include 2-hydroxyethyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, and (meth) acrylic. 6-hydroxyhexyl acid, 8-hydroxyoctyl (meth) acrylate, 10-hydroxydecyl (meth) acrylate, 12-hydroxylauryl (meth) acrylate, (4-hydroxymethylcyclohexyl) methyl (meth) acrylate, etc. Can be mentioned.
  • the energy beam polymerizable compound can be used in the range of, for example, 5 to 200 parts by weight, preferably 10 to 100 parts by weight, and more preferably 10 to 45 parts by weight with respect to 100 parts by weight of the base polymer.
  • a method for introducing an energy beam polymerizable double bond into a base polymer for example, when preparing an acrylic polymer as a base polymer, a copolymer having a reactive functional group such as a carboxyl group, a hydroxyl group, and an amino group And a method of copolymerizing a functional monomer.
  • a functional group serving as a base point of reaction is introduced into the base polymer, and a polyfunctional monomer or oligomer having an energy ray polymerizable carbon-carbon double bond is bonded via the functional group serving as the base point of the reaction.
  • a base polymer having an energy beam polymerizable carbon-carbon double bond in the side chain can be obtained.
  • the energy ray-curable pressure-sensitive adhesive may contain a photopolymerization initiator as necessary.
  • the photopolymerization initiator is excited and activated by irradiation with energy rays to generate radicals, and promotes an efficient polymerization and curing reaction of the pressure-sensitive adhesive layer.
  • Benzoin alkyl ether initiators such as benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, benzoin isobutyl ether;
  • Benzophenone initiators such as benzophenone, benzoylbenzoic acid, 3,3′-dimethyl-4-methoxybenzophenone, polyvinylbenzophenone; ⁇ -hydroxycyclohexyl phenyl ketone, 4- (2-hydroxyethoxy) phenyl (2-hydroxy-2-propyl) ketone, ⁇ -hydroxy- ⁇ , ⁇ '-dimethylacetophenone, methoxyacetophenone, 2,2-dimethoxy-2- Aromatic initiators such as phenylacetophenone and 2,2-diethoxyacetophenone; Aromatic ketal initiators such as benzyldimethyl ketal; Thioxanthone, 2-chlorothioxanthone
  • the pressure sensitive adhesive uses a polymer having an acidic group such as a carboxyl group as a base polymer, and a hydrophilicity is imparted by adding a neutralizing agent to neutralize all or part of the acidic groups in the base polymer. It is good also as an adhesive.
  • the hydrophilic adhesive generally has little adhesive residue on the adherend, and even when adhesive residue is generated, it can be easily removed by washing with pure water.
  • the polymer having an acidic group is obtained by copolymerizing a monomer having an acidic group such as the above-mentioned carboxyl group-containing monomer when preparing the base polymer.
  • neutralizing agent examples include primary amines such as monoethylamine and monoethanolamine, secondary amines such as diethylamine and diethanolamine, triethylamine, triethanolamine, N, N, N′-trimethylethylenediamine, N-methyldiethanolamine, Examples thereof include organic amino compounds exhibiting alkalinity, such as tertiary amines such as N, N-diethylhydroxylamine.
  • the pressure-sensitive adhesive may contain a crosslinking agent as required.
  • the crosslinking agent include an epoxy crosslinking agent, an isocyanate crosslinking agent, a melamine crosslinking agent, a peroxide crosslinking agent, a metal alkoxide crosslinking agent, a metal chelate crosslinking agent, a metal salt crosslinking agent, and a carbodiimide crosslinking.
  • Crosslinkers such as an agent, an oxazoline crosslinker, an aziridine crosslinker, and an amine crosslinker can be used, and an epoxy crosslinker, an isocyanate crosslinker, and the like can be preferably used. You may use these individually or in combination of 2 or more types.
  • epoxy crosslinking agent examples include N, N, N ′, N′-tetraglycidyl-m-xylenediamine, diglycidylaniline, 1,3-bis (N, N-glycidylaminomethyl) cyclohexane, 1,6 -Hexanediol diglycidyl ether, neopentyl glycol diglycidyl ether, ethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, sorbitol polyglycidyl ether, glycerol polyglycidyl ether, pentaerythritol Polyglycidyl ether, polyglycerol polyglycidyl ether, sorbitan polyglycidyl ether, trimethylolpropane polyglycidyl ether Ter, adipic acid digly
  • isocyanate-based crosslinking agents include lower aliphatic polyisocyanates such as 1,2-ethylene diisocyanate, 1,4-butylene diisocyanate, 1,6-hexamethylene diisocyanate; cyclopentylene diisocyanate, cyclohexylene diisocyanate, isophorone diisocyanate.
  • Aliphatic polyisocyanates such as hydrogenated tolylene diisocyanate and hydrogenated xylene diisocyanate; fragrances such as 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, 4,4′-diphenylmethane diisocyanate, xylylene diisocyanate Group polyisocyanates and the like.
  • the pressure-sensitive adhesive layer preferably contains a plasticizer.
  • the plasticizer include the same ones as described above.
  • the amount of the plasticizer added is suitably 10 to 100 parts by weight, preferably 10 to 100 parts by weight with respect to 100 parts by weight of the thermoplastic resin constituting the adhesive, that is, the base polymer. 80 parts by weight, more preferably 10 to 60 parts by weight is preferred.
  • the pressure-sensitive adhesive layer may further contain additives such as a stabilizer, a filler lubricant, a colorant, an ultraviolet absorber, an antioxidant, and a colorant as necessary. These additives include the same ones as described above.
  • the pressure-sensitive adhesive layer can be formed by applying the above-mentioned pressure-sensitive adhesive on a substrate by an appropriate method such as a knife coater, a roll coater, a gravure coater, a die coater, or a reverse coater. Further, for example, an adhesive layer may be formed on an appropriate casting process sheet such as a film having a release treatment applied to the surface, and the adhesive layer may be transferred onto the thermoplastic resin film.
  • the thickness of the pressure-sensitive adhesive layer is not particularly limited, but is preferably 5 to 100 ⁇ m, more preferably 5 to 60 ⁇ m, and particularly preferably 5 to 30 ⁇ m. When the thickness of the pressure-sensitive adhesive layer is within the above range, the stress of the thermoplastic resin film can be reduced and the stress relaxation rate of the pressure-sensitive adhesive tape can be improved.
  • the pressure-sensitive adhesive tape of the present invention preferably has, for example, a silicon wafer adhesive force that is suppressed to a fluctuation value within ⁇ 0.5 N / 20 mm before and after storage regardless of the storage state. From another point of view, it is preferable to suppress the fluctuation range within ⁇ 70% of the initial value, preferably within 65%, and more preferably within ⁇ 63%. By setting the fluctuation within such a range, it is possible to prevent the adhesive force of the adhesive tape from being lowered regardless of the storage state, there is no adhesive remaining on the adherend, and the adhesion from the adherend. Peeling can be easily performed.
  • the term “before storage” and “initial value” means immediately after the adhesive tape is manufactured or immediately after the adhesive tape is manufactured and the release liner is brought into contact with the adhesive layer side.
  • the term “after storage” usually means after about one week or more has elapsed since the production or when the release liner was brought into contact with the pressure-sensitive adhesive layer side.
  • This adhesive tape can be used for various purposes.
  • various members such as optical devices or films, products having a plate shape or curved surface made of resin, glass, metal, etc., for fixing wafers in semiconductor processes, for semiconductor back grinding, for semiconductor dicing, semiconductor package, glass
  • It can be used as a pressure-sensitive adhesive tape that is attached (further removed) for dicing ceramics, etc., and for protecting circuit surfaces during these processes.
  • the pressure-sensitive adhesive tape of the present invention can have various shapes and sizes such as a shape suitable for these applications, for example, a sheet shape and a strip shape.
  • the pressure-sensitive adhesive tape of the present invention contains both methylene bis-fatty acid amide and fatty acid in at least one of the thermoplastic resin film and the pressure-sensitive pressure-sensitive adhesive layer, resulting from the raw material / production method of methylene bis-fatty acid amide, etc.
  • substantially no fatty acid monoamide problems caused by using commercially available methylene bis fatty acid amide can be unexpectedly solved.
  • a fatty acid in addition to methylene bis-fatty acid amide it is possible to further balance the storage of the adhesive tape and the bonding and storage to the adherend. In other words, a sufficient adhesive force can always be obtained regardless of the storage state (that is, even by storage or processing at a high temperature).
  • a release liner In the pressure-sensitive adhesive tape of the present invention, in order to protect the pressure-sensitive adhesive layer, a release liner may be disposed on the pressure-sensitive adhesive layer side in contact with the pressure-sensitive adhesive layer.
  • a release liner if it is normally used in the said field
  • the thickness of the substrate is not particularly limited, and for example, 5 ⁇ m to 5 mm, preferably about 30 ⁇ m to 100 ⁇ m is appropriate.
  • silicone resin On the surface of such a substrate that is in contact with the pressure-sensitive adhesive layer, silicone resin, long chain alkyl resin, fluorine resin, low molecular weight polyethylene, polypropylene, rubber polymer, phosphate ester surfactant, etc.
  • silicone resin Long chain alkyl resin
  • fluorine resin low molecular weight polyethylene
  • polypropylene polypropylene
  • rubber polymer phosphate ester surfactant
  • phosphate ester surfactant etc.
  • Examples include those subjected to a release treatment known in the art, such as applying a mold in a layer form.
  • the release liner has one or more straight, wavy, serrated, and jagged slits (so-called back cuts) in order to improve the sticking operability when sticking the adhesive tape to the adherend. Also good.
  • the pressure-sensitive adhesive tape of the present invention uses a methylene bis fatty acid amide obtained by the reaction of a fatty acid amide and formaldehyde, preferably a solvent that dissolves the fatty acid monoamide and the fatty acid constituting it, but does not dissolve the methylene bis fatty acid amide.
  • Obtained methylene bis fatty acid amide purified by extraction, Adding the methylene bis-fatty acid amide and the fatty acid to the resin to form a thermoplastic resin film or a pressure-sensitive adhesive layer; It can manufacture by laminating
  • thermoplastic resin film or a pressure-sensitive adhesive layer by adding methylene bis fatty acid amide as an additive to a resin or the like a method of forming a thermoplastic resin film or a pressure-sensitive adhesive layer by adding a fatty acid
  • Methods known in the art can be used.
  • a melt extrusion method an inflation method, a T-die method, etc.
  • the pressure-sensitive adhesive layer may be separately formed by the method described above.
  • thermoplastic resin film or the pressure-sensitive adhesive layer may be performed simultaneously. That is, a thermoplastic resin film and a pressure-sensitive adhesive layer are multilayered by a co-extrusion method, a laminating method (extrusion laminating method, a laminating method using an adhesive, etc.), or a heat sealing method (external heating method, internal heating method, etc.). It may be formed as a structure.
  • the release liner can usually be obtained by forming a pressure-sensitive adhesive tape and then sticking it to the pressure-sensitive adhesive layer side to obtain a pressure-sensitive adhesive tape with a release liner.
  • Thermoplastic resin 100 parts by weight of polyvinyl chloride resin (average degree of polymerization 1050)
  • Plasticizer 30 parts by weight of diethylhexyl phthalate
  • Stabilizer 3 parts by weight of Ba-Zn mixed stabilizer 0.7 part by weight of lubricant
  • An adhesive was prepared with the following composition.
  • Plasticizer Diethylhexyl phthalate 20 parts by weight
  • Crosslinking agent Butylated melamine resin 10 parts by weight
  • the obtained pressure-sensitive adhesive was diluted to 20% with toluene, and the thickness after drying was 10 ⁇ m. It apply
  • a release liner silicone-treated polyester film, MRF, 38 ⁇ m (manufactured by Mitsubishi Plastics)
  • Measuring device Instron type tensile tester AUTOGRAPH AG-IS made by Shimadzu Corporation Measurement atmosphere: 23 ° C., 50% RH Substrate: 8-inch mirror wafer Bonding condition: 1 reciprocation with 2 kg roller Measurement condition: 90 ° peel, 300 mm / min Pass / fail judgment: A value within ⁇ 0.5 N / 20 mm with respect to the initial value was accepted.
  • Palmitic acid Reagent grade 95% or higher
  • Stearic acid monoamide Reagent grade 95% or higher Palmitic acid monoamide: Reagent grade 95% or higher
  • the pressure-sensitive adhesive tape of the present invention can be widely used as a surface protection tape or sheet for various adherends such as electronic parts, a processing tape for protection during dicing, or a protection tape or sheet.

Landscapes

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

Abstract

L'invention a pour objectif de fournir un ruban adhésif qui tout en permettant d'obtenir des caractéristiques d'adhérence et de décollement stables dans divers environnements, permet de réduire à un minimum la pollution d'un support. Plus précisément, ce ruban adhésif est constitué par formation d'une couche adhésive sensible à la pression sur une des faces d'un film de résine thermoplastique. Un méthylènebis amide d'acide gras et un acide gras sont compris au moins dans le film de résine thermoplastique et/ou la couche adhésive sensible à la pression, mais aucun monoamide d'acide gras en tant que sous-produit lors de la production du méthylènebis amide d'acide gras, n'est sensiblement compris dans le ruban adhésif.
PCT/JP2013/055103 2012-02-27 2013-02-27 Ruban adhésif WO2013129462A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201380007921.4A CN104093804A (zh) 2012-02-27 2013-02-27 粘合带

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2012-040166 2012-02-27
JP2012040166A JP2013173876A (ja) 2012-02-27 2012-02-27 粘着テープ

Publications (1)

Publication Number Publication Date
WO2013129462A1 true WO2013129462A1 (fr) 2013-09-06

Family

ID=49082656

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2013/055103 WO2013129462A1 (fr) 2012-02-27 2013-02-27 Ruban adhésif

Country Status (4)

Country Link
JP (1) JP2013173876A (fr)
CN (1) CN104093804A (fr)
TW (1) TW201343861A (fr)
WO (1) WO2013129462A1 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6390034B2 (ja) * 2014-08-01 2018-09-19 リンテック株式会社 粘着シート
US20190048233A1 (en) * 2016-02-01 2019-02-14 3M Innovative Properties Company Conformable, peelable adhesive articles

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57139163A (en) * 1981-02-24 1982-08-27 Nitto Electric Ind Co Ltd Adhesive sheet or tape
JP2006219520A (ja) * 2005-02-08 2006-08-24 Nitto Denko Corp 表面保護シート、およびその製造方法
JP2011208087A (ja) * 2010-03-30 2011-10-20 Nitto Denko Corp ロール状粘着テープ又はシート
JP2011208086A (ja) * 2010-03-30 2011-10-20 Nitto Denko Corp 剥離ライナー付き粘着テープ又はシート
WO2012005317A1 (fr) * 2010-07-09 2012-01-12 日東電工株式会社 Composition de méthylènebis(amide d'acide gras), feuille adhésive sensible à la pression et son procédé de fabrication

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57139163A (en) * 1981-02-24 1982-08-27 Nitto Electric Ind Co Ltd Adhesive sheet or tape
JP2006219520A (ja) * 2005-02-08 2006-08-24 Nitto Denko Corp 表面保護シート、およびその製造方法
JP2011208087A (ja) * 2010-03-30 2011-10-20 Nitto Denko Corp ロール状粘着テープ又はシート
JP2011208086A (ja) * 2010-03-30 2011-10-20 Nitto Denko Corp 剥離ライナー付き粘着テープ又はシート
WO2012005317A1 (fr) * 2010-07-09 2012-01-12 日東電工株式会社 Composition de méthylènebis(amide d'acide gras), feuille adhésive sensible à la pression et son procédé de fabrication

Also Published As

Publication number Publication date
JP2013173876A (ja) 2013-09-05
TW201343861A (zh) 2013-11-01
CN104093804A (zh) 2014-10-08

Similar Documents

Publication Publication Date Title
US20110244160A1 (en) Adhesive tape or sheet with release liner
CN103205225B (zh) 粘合剂用聚合物、粘合剂组合物和热剥离性粘合片
WO2012121155A1 (fr) Bande ou feuille adhésive
JP5572418B2 (ja) 積層セラミックシート切断用熱剥離型粘着シート
JP2011208087A (ja) ロール状粘着テープ又はシート
US20080038551A1 (en) Warpage-inhibitive pressure-sensitive adhesive sheets for wafer grinding
TWI553083B (zh) 壓敏性膠黏膜及使用彼之背面研磨法
JP5406110B2 (ja) 半導体ウエハ加工用粘着シート
JP5635825B2 (ja) メチレンビス脂肪酸アミド組成物、粘着シート及びその製造方法
EP2792725A1 (fr) Composition de résine adhésive, corps stratifié, et procédé d'auto-décollement
WO2013129463A1 (fr) Ruban adhésif
WO2013129462A1 (fr) Ruban adhésif
JP2004346296A (ja) 放射線硬化型再剥離用水分散型アクリル系粘着剤組成物および放射線硬化再剥離型アクリル系粘着シート
JP2013173874A (ja) 粘着テープ
JP7509581B2 (ja) 半導体加工用粘着シート
JP6550271B2 (ja) バックグラインドテープ
WO2022270008A1 (fr) Feuille adhésive pour la fabrication d'éléments semi-conducteurs
KR20170079563A (ko) 분리막

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 13755763

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 13755763

Country of ref document: EP

Kind code of ref document: A1