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WO2013008861A1 - Composition de résine et film antiadhésif - Google Patents

Composition de résine et film antiadhésif Download PDF

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Publication number
WO2013008861A1
WO2013008861A1 PCT/JP2012/067746 JP2012067746W WO2013008861A1 WO 2013008861 A1 WO2013008861 A1 WO 2013008861A1 JP 2012067746 W JP2012067746 W JP 2012067746W WO 2013008861 A1 WO2013008861 A1 WO 2013008861A1
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WO
WIPO (PCT)
Prior art keywords
release
release film
propylene
ethylene
resin composition
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.)
Ceased
Application number
PCT/JP2012/067746
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English (en)
Japanese (ja)
Inventor
可奈子 池田
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.)
Mitsubishi Chemical Corp
Original Assignee
Mitsubishi Chemical Corp
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 Mitsubishi Chemical Corp filed Critical Mitsubishi Chemical Corp
Priority to KR1020147000467A priority Critical patent/KR20140038509A/ko
Priority to CN201280034091.XA priority patent/CN103649204A/zh
Publication of WO2013008861A1 publication Critical patent/WO2013008861A1/fr
Anticipated expiration legal-status Critical
Ceased 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
    • C09J123/00—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
    • C09J123/02—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
    • 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
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C33/00—Moulds or cores; Details thereof or accessories therefor
    • B29C33/56—Coatings, e.g. enameled or galvanised; Releasing, lubricating or separating agents
    • B29C33/60—Releasing, lubricating or separating agents
    • B29C33/62—Releasing, lubricating or separating agents based on polymers or oligomers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C33/00—Moulds or cores; Details thereof or accessories therefor
    • B29C33/56—Coatings, e.g. enameled or galvanised; Releasing, lubricating or separating agents
    • B29C33/68—Release sheets
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10—Homopolymers or copolymers of propene
    • C08L23/12—Polypropene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10—Homopolymers or copolymers of propene
    • C08L23/14—Copolymers of propene
    • 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
    • C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
    • C09J4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09J159/00 - C09J187/00
    • 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
    • C09J7/40—Adhesives in the form of films or foils characterised by release liners
    • C09J7/401—Adhesives in the form of films or foils characterised by release liners characterised by the release coating 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
    • C09J2423/00—Presence of polyolefin
    • C09J2423/04—Presence of homo or copolymers of ethene
    • C09J2423/045—Presence of homo or copolymers of ethene in the release coating
    • 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
    • C09J2423/00—Presence of polyolefin
    • C09J2423/10—Presence of homo or copolymers of propene
    • C09J2423/105—Presence of homo or copolymers of propene in the release coating
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2453/00—Presence of block copolymer
    • C09J2453/005—Presence of block copolymer in the release coating

Definitions

  • the present invention relates to a resin composition and a release film having good release properties.
  • the present invention relates to a release film suitable for surface protection of various members and a resin composition suitable as a release layer for the release film.
  • the present invention relates to a release film for surface protection suitable for protecting the surface of a building member, an automobile member, a display member and the like, and a resin composition suitable as a release layer for the release film for surface protection.
  • the present invention relates to a release film for surface protection suitable for protecting the surface of a resin, metal, glass or the like, and a resin composition suitable for a release layer of the release film for surface protection.
  • release films are frequently used for double-sided adhesive tapes, single-sided adhesive tapes with release films, product protective films, and the like.
  • a release film conventionally, a method of applying a release agent such as a silicone compound, a long chain alkyl compound, polyvinyl alcohol or carbamate to the surface of a substrate such as a resin film or paper has been adopted.
  • a release agent such as a silicone compound, a long chain alkyl compound, polyvinyl alcohol or carbamate
  • the type of release film that applies such a release agent to the substrate is difficult to apply uniformly, and it is difficult to control the release force, or when the release film is rolled.
  • the problem is that the release agent is transferred to the facing adhesive layer side and the re-adhesiveness (adhesive strength of the adhesive layer after the release film is peeled off) is lowered.
  • a release film using a polyolefin resin crosslinked with polysiloxane see Patent Document 1
  • a release film containing a fatty acid amide compound in a polyethylene resin see Patent Document 2
  • blended the mold release agent in resin, such as the release film (refer patent document 3) containing the fatty acid bisamide type compound in the propylene-type polymer is disclosed.
  • an agricultural film comprising a resin composition obtained by adding a fatty acid bisamide compound to an ethylene- ⁇ -olefin copolymer has been disclosed (see Patent Document 4).
  • the release film in the above-mentioned adhesive tape, protective film, etc. it is important to protect the adhesive surface and have good release properties for the adhesive, but in recent release films, It is required to have a uniform releasability at a higher level.
  • a wide tape is formed by forming a wide tape and then cutting it with equally spaced slits.
  • a large area protective film is required, but these require uniform adhesiveness and releasability. Yes.
  • release films are usually produced by co-extrusion molding or extrusion laminate molding.
  • the adhesive layer adheres firmly to the facing release layer.
  • the film cannot be fed out from the roll (unwinding property is poor).
  • a release film having uniform and appropriate release properties, good re-adhesiveness of the adhesive layer, and good roll unwinding properties by coextrusion molding is obtained. It was not clear how it could be achieved.
  • An object of the present invention is to provide a release film and a resin composition having good release properties.
  • the present invention provides a release film having uniform and appropriate release properties, good re-adhesiveness of the adhesive layer, and good roll unwinding property even by coextrusion molding, It is an object to provide a resin composition suitable as a release layer of a release film.
  • an object of the present invention is to provide a release film suitable for protecting the surface of various members and a resin composition suitable as a release layer for the release film.
  • the present invention provides a release film for surface protection suitable for protecting the surface of a building member, automobile member, display member, etc., and a resin composition suitable as a release layer for the release film for surface protection. Is an issue.
  • the present invention also provides a release film for surface protection suitable for protecting the surface of synthetic resin, metal, glass and the like, and a resin composition suitable as a release layer for the release film for surface protection. Let it be an issue.
  • the present inventor can solve the above problems by incorporating a fatty acid bisamide compound having a specific chemical structure into a polyolefin resin having a specific bending elastic modulus. As a result, the present invention has been completed.
  • a resin composition comprising a polyolefin resin (A) having a flexural modulus of 800 MPa or less and a fatty acid bisamide compound (B) represented by the following general formula (1).
  • R—CONH— (CH 2 ) n —NHCO—R (1) (In the formula, n represents an integer of 1 to 6, and each R independently represents an aliphatic group having 19 or more carbon atoms.)
  • n represents an integer of 1 to 6, and each R independently represents an aliphatic group having 19 or more carbon atoms.
  • n represents an integer of 1 to 6, and each R independently represents an aliphatic group having 19 or more carbon atoms.
  • n represents an integer of 1 to 6, and each R independently represents an aliphatic group having 19 or more carbon atoms.
  • the release film and resin composition which have favorable mold release property can be provided.
  • a release film having uniform and appropriate release properties, good re-adhesiveness of the adhesive layer, and good roll unwinding property even by coextrusion molding, and the release film A resin composition suitable as a mold release layer can be provided.
  • a release film for surface protection suitable for protecting the surface of a building member, an automobile member, a display member, etc., and a resin composition suitable as a release layer of the release film for surface protection are provided. can do.
  • the present invention also provides a release film for surface protection suitable for protecting the surface of synthetic resin, metal, glass and the like, and a resin composition suitable as a release layer for the release film for surface protection. it can.
  • release does not mean only release from a specific shape, but is synonymous with “peel”.
  • the resin composition of the present invention contains a polyolefin resin (A) and a fatty acid bisamide compound (B).
  • the release film of the present invention has at least a release layer containing the resin composition.
  • the polyolefin resin used as the polyolefin resin (A) is not particularly limited.
  • a homopolymer such as ethylene, propylene, 1-butene; a copolymer of the homopolymers; or the homopolymer and 3-methyl- Other ⁇ -olefins having about 4 to 20 carbon atoms such as 1-butene, 1-pentene, 4-methyl-1-pentene, 1-hexene, 1-octene, 1-decene, (meth) acrylic acid, methyl
  • examples thereof include various (meth) acrylates such as (meth) acrylate, polar monomers such as vinyl acetate, vinyl alcohol, and maleic anhydride, and styrene monomers such as styrene and styrene derivatives.
  • (meth) acrylic acid means acrylic acid or methacrylic acid, and the same applies to (meth) acrylate.
  • polyolefin resins may be modified with an unsaturated carboxylic acid such as maleic anhydride, maleic acid or acrylic acid or a derivative thereof, an unsaturated silane compound, or the like. Furthermore, you may have a crosslinked structure partially.
  • the chain form in the case of using a copolymer as the polyolefin resin is not limited and may be any of a block copolymer, a random copolymer, a graft copolymer, and the like.
  • These polyolefin resins may be used individually by 1 type, or may use 2 or more types together.
  • the polyolefin resin (A) in the present invention is a polyolefin resin having a flexural modulus of 800 MPa or less.
  • the flexural modulus of the polyolefin resin exceeds the above upper limit, the releasability and uniformity of the release film are lowered.
  • the cause of this is not clear, but it is considered that the polyolefin resin having a low flexural modulus has a low crystallinity, and this low crystallinity contributes to good and uniform release properties.
  • the presence of a certain amount or more of the amorphous region of the polyolefin resin has good affinity with the fatty acid bisamide compound (B) described later.
  • the above-described polyolefin resin may be appropriately selected and prepared so that the flexural modulus is 800 MPa or less.
  • the upper limit value of the flexural modulus of the polyolefin resin is preferably 700 MPa or less, more preferably 650 MPa or less, and further preferably 600 MPa or less, for the same reason as described above.
  • the flexural modulus of the polyolefin resin is a value measured according to JIS K7203 (1995) (the same applies to the following measurements).
  • the lower limit of the flexural modulus of the polyolefin resin is not limited, but is usually 5 MPa or more, preferably 10 MPa or more, more preferably 15 MPa or more. When the flexural modulus of the polyolefin resin is less than the lower limit, the moldability tends to decrease and the mechanical properties of the release film tend to decrease.
  • propylene polymer As one aspect
  • the propylene-based polymer used as the polyolefin resin (A) is not limited as long as it has a propylene monomer unit, that is, polymerized using propylene as one component of a raw material monomer. Is a polymer having 50% by weight or more, preferably 70% by weight or more, more preferably 80% by weight or more.
  • the propylene monomer unit constituting the propylene-based polymer is at least the lower limit value, the release property and uniformity of the obtained release film tend to be optimized.
  • the upper limit of the propylene monomer unit constituting the propylene-based polymer is not limited and may be a propylene homopolymer, but preferably 98% by weight or less, more preferably 95% by weight or less of the propylene monomer unit. Further, a copolymer having 90% by weight or less is more preferable.
  • the propylene monomer unit constituting the propylene-based polymer is set to the upper limit value or less, it becomes easier to achieve the bending elastic modulus required for the polyolefin resin (A). For this reason, when it is set as a release film, it exists in the tendency for the mold release property and its uniformity to become favorable.
  • the propylene-based polymer used in the present invention may be a propylene homopolymer as described above.
  • isotactic homopolypropylene and syndiotactic homopolypropylene can achieve the bending elastic modulus defined in the present invention. Have difficulty. Therefore, when a propylene homopolymer is used as the polyolefin resin (A), one having a reduced tacticity is usually used.
  • a propylene-based polymer is used as the polyolefin resin (A), it is preferably a copolymer of a propylene monomer and another monomer as compared with a propylene homopolymer.
  • the monomer copolymerized with propylene is not limited as long as it is a compound copolymerizable with propylene.
  • ethylene 1-butene, 1-pentene, 3-methyl-1-butene, 1- Carbons such as hexene, 4-methyl-1-pentene, 3-methyl-1-pentene, 1-heptene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicosene, etc.
  • ⁇ -olefins having a number of about 4 to 20; (meth) acrylic acid; various (meth) acrylates such as methyl (meth) acrylate; polar monomers such as vinyl acetate, vinyl alcohol, maleic anhydride; styrene, styrene derivatives, etc. Examples thereof include styrene monomers.
  • (meth) acrylic acid means acrylic acid or methacrylic acid, and the same applies to the (meth) acrylate.
  • These monomers may be used alone or in combination of two or more.
  • the monomer copolymerized with propylene ethylene and an ⁇ -olefin having about 4 to 20 carbon atoms are preferable.
  • Such a copolymer is not limited, and specifically, a propylene / ethylene copolymer, a propylene / 1-butene copolymer, a propylene / ethylene / 1-butene copolymer, a propylene / 4-methyl-1 -A pentene copolymer, a copolymer of propylene and other ⁇ -olefin, a copolymer of propylene and a polar monomer, and the like.
  • Each of these copolymers may be not only a random copolymer but also a block copolymer, a graft copolymer, or the like.
  • the propylene chain portion may be any of isotactic, syndiotactic, atactic, stereoblock and the like.
  • a well-known thing can be suitably employ
  • the propylene polymer in the present invention may be modified with an unsaturated carboxylic acid or a derivative thereof, an unsaturated silane compound, or the like. Furthermore, you may have a crosslinked structure partially.
  • the propylene polymer a propylene / ethylene copolymer, a propylene / 1-butene copolymer, and a propylene / ethylene / 1-butene copolymer are preferable.
  • the propylene polymer may be used in combination of two or more of the above resins, or a propylene polymer and a polyolefin other than the propylene polymer may be used in combination.
  • the propylene polymer in the present invention has a flexural modulus of 800 MPa or less.
  • the bending elastic modulus of the propylene-based polymer exceeds the upper limit value, the releasability and the uniformity thereof when used as a release film are lowered.
  • the cause of this is not clear, but propylene polymers with low flexural modulus have low crystallinity, and this low crystallinity is considered to contribute to good and uniform release. .
  • it is considered that the presence of a certain amount or more of the amorphous region of the propylene polymer has good affinity with the fatty acid bisamide compound (B) described later.
  • the upper limit value of the flexural modulus of the propylene-based polymer is preferably 700 MPa or less, more preferably 650 MPa or less, and further preferably 600 MPa or less, for the same reason as described above.
  • the lower limit of the flexural modulus of the propylene-based polymer is not limited, but is usually 5 MPa or more, preferably 10 MPa or more, more preferably 15 MPa or more. When the flexural modulus of the propylene polymer is less than the lower limit value, the moldability tends to be lowered and the mechanical properties of the release film tend to be lowered.
  • the melt flow rate (MFR) of the propylene-based polymer is not particularly limited, but is usually 0.5 to 50 g / 10 minutes, preferably 1 to 30 g / 10 at 230 ° C. and a load of 2.16 kg (21.18 N). Min, more preferably 2 to 25 g / 10 min.
  • MFR melt flow rate
  • [Propylene / ethylene-block copolymer] it is suitable to use the block copolymer which is one aspect
  • a block copolymer composed of a propylene block and at least one block of ethylene and ⁇ -olefin hereinafter referred to as “a propylene block and at least one block of ethylene and ⁇ -olefin”.
  • ⁇ -olefins examples include ⁇ -olefins having about 4 to 20 carbon atoms.
  • the at least one block of ethylene and ⁇ -olefin is not only a polymer block of ethylene alone, a polymer block of ⁇ -olefin alone, but also a copolymer block of ethylene and ⁇ -olefin, 2
  • a block having two or more different ⁇ -olefins is also included, and propylene is also included as a structural unit thereof.
  • the propylene / ethylene-block copolymer usually has a domain of a propylene polymer block and a domain of at least one polymer block of ethylene and ⁇ -olefin.
  • the releasability and uniformity of the release film using the resin composition of the present invention are improved. It tends to be excellent in impact resistance and rigidity.
  • a preferred embodiment of the propylene / ethylene-block copolymer includes a block copolymer containing a propylene homopolymer portion (a) and an ethylene / propylene-random copolymer portion (b).
  • the content ratio of the propylene homopolymer part (a) and the ethylene / propylene-random copolymer part (b) is not limited, but the propylene homopolymer part (a) is 20 to 50% by weight, and the ethylene / propylene / random copolymer part.
  • B) is preferably 80 to 50% by weight.
  • the content ratio of the propylene homopolymer part (a) is within the above range, the mold release property and uniformity thereof when using the resin composition of the present invention as a release film are improved and the chemical resistance is improved. In some cases, it is excellent in impact resistance, rigidity, and the like.
  • the preferred range of the content ratio of the propylene homopolymer part (a) and the ethylene / propylene-random copolymer part (b) is 30 to 45% by weight of the propylene homopolymer part (a) for the same reason as above.
  • the propylene-random copolymer part (b) is 70 to 55% by weight.
  • the ethylene content in the propylene / ethylene-random copolymer part (b) is not limited and may be composed only of an ⁇ -olefin containing propylene, but the ethylene content is preferably 40 to 70% by weight.
  • the ethylene content is within the above range, the mold release property and uniformity thereof when using the resin composition of the present invention are good, and the impact resistance and rigidity are excellent. There is a case.
  • the flexural modulus of the polyolefin resin (A) in the present invention is 800 MPa or less.
  • the polyolefin resin (A) a propylene homopolymer part (a), an ethylene / propylene-random copolymer part (b), and
  • the bending elastic modulus of the ethylene / propylene-random copolymer portion (b) may be 800 MPa or less. That is, when the flexural modulus of the ethylene / propylene-random copolymer portion (b) is 800 MPa or less, the case where the overall flexural modulus of the block copolymer exceeds 800 MPa is also included.
  • the propylene / ethylene-block copolymer usually has a domain of a propylene polymer block and a domain of at least one polymer block of ethylene and ⁇ -olefin.
  • This phase is present independently, so that the effect of the present invention can be obtained if the flexural modulus of the ethylene / propylene-random copolymer portion (b) is 800 MPa or less.
  • the flexural modulus of the ethylene / propylene-random copolymer part (b) is preferably 700 MPa or less, more preferably 650 MPa or less, and further preferably 600 MPa or less for the same reason as described above.
  • the lower limit of the flexural modulus of the ethylene / propylene-random copolymer part (b) is not limited, but is usually 5 MPa or more, preferably 10 MPa or more, more preferably 15 MPa or more.
  • the flexural modulus of the ethylene / propylene-random copolymer part (b) is less than the lower limit, the moldability tends to be lowered and the mechanical properties of the release film tend to be lowered.
  • a block copolymer containing a propylene homopolymer part (a) and an ethylene / propylene / random copolymer part (b) as a method for confirming the bending elastic modulus of the ethylene / propylene / random copolymer part (b) May produce a copolymer having a composition corresponding only to the ethylene / propylene-random copolymer part (b) and measure the flexural modulus thereof. If the block copolymer can be separated into a propylene homopolymerized portion (a) and an ethylene / propylene-random copolymerized portion (b) by dissolving in a solvent, this can be separated and recovered. You may measure a bending elastic modulus. Examples of the conditions for fractionation include a method of extracting at 150 to 200 ° C. using orthodichlorobenzene as a solvent.
  • the method for producing the propylene / ethylene-block copolymer is not limited, but it is usually produced by slurry polymerization, gas phase polymerization or liquid phase bulk polymerization using a highly stereoregular catalyst.
  • the polymerization method is batch polymerization. Both types of continuous polymerization can be employed.
  • a propylene homopolymer part (a) is first formed by homopolymerization of propylene, and then a random copolymer of ethylene with at least one of ⁇ -olefin and propylene.
  • an ethylene / propylene-random copolymer portion (b) formed by polymerization is preferred.
  • propylene homopolymerization is performed using a catalyst in which an organic aluminum compound component is combined with a solid component formed by contacting magnesium tetrachloride with titanium tetrachloride, an organic acid halide, and an organic silicon compound, and then ethylene and propylene are combined. It can manufacture by performing random copolymerization.
  • the propylene / ethylene-block copolymer may be a ternary or higher copolymer containing other unsaturated compounds, for example, vinyl esters such as vinyl acetate, within the range not impairing the effects of the present invention, Moreover, these mixtures may be sufficient.
  • propylene / ethylene-block copolymers examples include “Zeras 7023” manufactured by Mitsubishi Chemical Corporation, “Novatech PP BC3H” manufactured by Nippon Polypro Co., Ltd., “Cataloy CA7320A” manufactured by Sun Allomer, “Cataloy Adflex C200F”, and the like. It can be used suitably.
  • Polyolefin resin other than propylene polymer (A) examples include the following. Specifically, low, medium and high density polyethylene (branched or straight chain) ethylene homopolymers, ethylene / propylene copolymers, ethylene / 1-butene copolymers, ethylene / 4-methyl, etc.
  • ethylene / 1-pentene copolymer ethylene / 1-hexene copolymer, ethylene / 1-octene copolymer, ethylene / vinyl alcohol copolymer (including saponified ethylene / vinyl acetate copolymer), ethylene / ( Ethylene polymers such as (meth) acrylic acid copolymers; 1-butene homopolymers, 1-butene polymers such as 1-butene / ethylene copolymers, 1-butene / propylene copolymers; Examples include so-called cyclic polyolefin resins such as ring metathesis polymers, norbornene derivatives and ethylene copolymers.
  • the ethylene polymer means a polymer containing ethylene as a main component as a raw material monomer, preferably containing 50% by weight or more of ethylene, and the same applies to a 1-butene polymer.
  • the polyolefin resin other than the propylene-based polymer used as the polyolefin resin (A) is a resin having a flexural modulus of 800 MPa or less, preferably 700 MPa or less, more preferably 650 MPa or less, and even more preferably 600 MPa or less. Is selected.
  • the lower limit of the flexural modulus is not limited, but is usually 5 MPa or more, preferably 10 MPa or more, more preferably 15 MPa or more.
  • the melt flow rate (MFR) of the polyolefin resin other than the propylene-based polymer used as the polyolefin resin (A) is not limited, but is usually 0.5 to 50 g / 10 minutes, preferably 1 to 30 g / 10 minutes, more preferably 2 ⁇ 25 g / 10 min.
  • MFR means a value at 230 ° C. and 21.2 N load as described above, but the polyolefin resin (A) is an ethylene polymer, 1 In the case of a butene polymer or other polyolefin resin, it means a value at 190 ° C. and 21.2 N load.
  • the MFR of the polyolefin resin (A) is smaller than the lower limit value, or exceeds the upper limit value, in any case, the moldability when producing the release film of the present invention may be insufficient. is there.
  • polyolefin resin (A) 4 weight% or more of components other than propylene are contained in polyolefin resin (A).
  • the measuring method of components other than propylene in polyolefin resin (A) can be implemented with the following procedures.
  • -Extraction method of release layer component from film Using a polarizing microscope, cross-sectional observation is performed to measure the release layer thickness in the film. Peel off the release layer using a blade or the like. At this time, the film may be immersed in a solvent such as ethanol or acetone, swollen, and peeled off.
  • -Components other than propylene (C3) are calculated
  • the release layer extracted from the film is completely protonated and measured according to the following conditions by a coupling method. It can be determined by analyzing a 13 C-NMR spectrum.
  • a coupling method for example, GSX-400 manufactured by JEOL Ltd. or an equivalent device (carbon nuclear resonance frequency of 100 MHz or more) can be used, and the measurement conditions are as follows.
  • [PPP] k ⁇ I (T ⁇ ) (a)
  • [PPE] k ⁇ I (T ⁇ ) (b)
  • [EPE] k ⁇ I (T ⁇ ) (c)
  • [PEP] k ⁇ I (S ⁇ ) (d)
  • [PEE] k ⁇ I (S ⁇ ) (e)
  • [EEE] k ⁇ ⁇ I (S ⁇ ) / 2 + I (S ⁇ ) / 4 ⁇ (f)
  • square brackets “[]” indicate the fraction of triads, for example, [PPP] is the fraction of PPP triads in all triads.
  • [PPP] + [PPE] + [EPE] + [PEP] + [PEE] + [EEE] 1 (g) It is. Further, k is a coefficient, I indicates a spectral intensity, and for example, I (T ⁇ ) means a peak intensity of 28.7 ppm assigned by T ⁇ .
  • Ethylene content (mol%) ([PEP] + [PEE] + [EEE]) ⁇ 100
  • the conversion of the ethylene content from mole% to weight% is performed using the following formula.
  • Ethylene content (% by weight) (28 ⁇ X / 100) / ⁇ 28 ⁇ X / 100 + 42 ⁇ (1 ⁇ X / 100) ⁇ ⁇ 100
  • X is the ethylene content in mol%.
  • the method described here is a method for obtaining the ethylene content, and the content of components other than ethylene can be converted by assigning a spectrum to each.
  • the fatty acid bisamide compound (B) in the present invention is a compound represented by the following general formula (1).
  • the aliphatic groups R at both ends may be the same or different, but are preferably the same for ease of production.
  • the chemical structure of the aliphatic group R represented by the general formula (1) affects the release performance. Since the fatty acid bisamide compound (B) in the present invention is a fatty acid bisamide compound having an aliphatic group having 19 or more carbon atoms at both ends, it can form a crystal structure with little disturbance. For this reason, when the release layer containing the fatty acid bisamide compound (B) comes into contact with the adhesive layer, the entanglement of molecules between both layers is suppressed, and good release performance can be exhibited.
  • a release layer containing the fatty acid bisamide compound (B) when the adhesive layer is coated and dried on the release layer to receive heat, Even when it is stored in a high temperature environment in a bonded state, it is possible to exhibit good release performance. This is because the fatty acid bisamide compound (B) has a high melting temperature, so that its crystal structure can be maintained even at high temperatures, and molecular entanglement with the adhesive substance is suppressed. As a result, stable release characteristics can be exhibited over time.
  • each is preferably selected from fatty acid bisamide compounds having an aliphatic group having 19 to 27 carbon atoms, more preferably 19 to 23 carbon atoms, and still more preferably 21 to 23 carbon atoms.
  • the fatty acid bisamide compound in which the aliphatic group has the carbon number within the above range sufficient release performance is obtained, and when producing a resin composition or a release film with the polyolefin resin (A), fuming or foaming is produced. This is preferable because it is difficult to cause such problems.
  • Each of the two aliphatic groups (R in the above formula) in the fatty acid bisamide compound may be a linear aliphatic group or a branched aliphatic group, but is preferably a linear aliphatic group.
  • the release performance is good. The reason is not clear, but it is considered that the fatty acid bisamide compound having a linear aliphatic group having 19 or more carbon atoms can form a crystal structure with less disturbance.
  • Each of the two aliphatic groups (R in the above formula) in the fatty acid bisamide compound may be a saturated aliphatic group or an unsaturated aliphatic group, but is preferably a saturated aliphatic group.
  • Examples of the aliphatic group include nonadecyl group, icosanyl group, heneicosanyl group, docosanyl group, and tricosanyl group.
  • an alkyl group having 21 to 23 carbon atoms is preferable, and specifically, heicosanyl group and tricosanyl group are particularly preferable.
  • the fatty acid bisamide compound (B) has a divalent linking group for linking two amide groups (corresponding to the — (CH 2 ) n — moiety in the above formula).
  • this bivalent coupling group is not specifically limited, A methylene group, ethylene group, trimethylene group, tetramethylene group, hexamethylene group is mentioned, Preferably it is a methylene group or ethylene group.
  • a compound corresponding to the general formula (1) may be used alone, or two or more different compounds may be used in combination. Moreover, in this invention, you may use together fatty acid bisamide compounds other than the said General formula (1).
  • R is a linear aliphatic group having 18 or less carbon atoms
  • the fatty acid bisamide compound in the present invention can be produced by a general method of amidating a predetermined fatty acid and a predetermined alkylene diamine according to a conventional method.
  • the fatty acid bisamide compound obtained by amidation may be purified by a conventional method.
  • a general method for producing a fatty acid bisamide compound for example, a temperature of 100 to 250 ° C. under normal pressure or pressurization in an inert gas atmosphere, an alkali borohydride compound, phosphorous acid, hypophosphorous acid or It can be produced by reacting a fatty acid with an alkylene diamine in the presence of these alkali metal salts or alkaline earth metal salts.
  • the fatty acid as the raw material is preferably a fatty acid having 20 or more carbon atoms, preferably 20 to 28 carbon atoms, more preferably 20 to 24 carbon atoms, and still more preferably 22 to 24 carbon atoms.
  • Examples thereof include arachidic acid and behenic acid.
  • Examples include acids and lignoceric acid. Preferred are behenic acid and lignoceric acid.
  • various molecular structures of the fatty acid bisamide obtained can be obtained, but if the fatty acid bisamide corresponding to the general formula (1) is included, It may be a mixture of fatty acid bisamides having different molecular structures.
  • alkylene diamine examples include alkylene diamines having 1 to 6 carbon atoms. Examples thereof include methylene diamine, ethylene diamine, trimethylene diamine, tetramethylene diamine, and hexamethylene diamine. Preferred are methylene diamine and ethylene diamine, and more preferred is ethylene diamine.
  • resins other than the polyolefin resin (A) include polyolefins not included in the polyolefin resin (A); polyphenylene ether resins; polyamide resins such as nylon 6, nylon 66, and nylon 11; polycarbonate resins Polyester resins such as polyethylene terephthalate and polybutylene terephthalate; (meth) acrylic resins such as polymethyl methacrylate; thermoplastic resins such as styrene resins such as polystyrene; and various thermoplastic elastomers.
  • polyolefins not included in the polyolefin resin (A) include propylene homopolymers which are propylene polymers having a flexural modulus of more than 800 MPa.
  • the resin composition of the present invention is preferably used in combination with a polyolefin resin (A) and a propylene-based polymer having a flexural modulus exceeding 800 MPa.
  • additives include various heat stabilizers, antioxidants, ultraviolet absorbers, light stabilizers, anti-aging agents, nucleating agents, plasticizers, impact modifiers, compatibilizers, antifoaming agents, Examples thereof include a sticking agent, a crosslinking agent, a surfactant, a lubricant, an antiblocking agent, a processing aid, an antistatic agent, a flame retardant, a flame retardant aid, a filler, a colorant, and an inorganic crystal nucleating agent. Moreover, you may contain mold release agents other than a fatty-acid bisamide compound. These other resins and additives may be used alone or in combination of two or more in any combination and ratio.
  • Non-halogen flame retardants include phosphorus flame retardants, hydrated metal compounds (aluminum hydroxide and magnesium hydroxide) flame retardants, nitrogen-containing compounds (melamine and guanidine) flame retardants and inorganic compounds (borate and molybdenum) Compound) flame retardant and the like.
  • ⁇ Fillers are roughly classified into organic fillers and inorganic fillers.
  • the organic filler include naturally occurring polymers such as starch, cellulose fine particles, wood flour, okara, fir husk, bran, and modified products thereof.
  • Inorganic fillers include talc, calcium carbonate, zinc carbonate, wollastonite, silica, alumina, magnesium oxide, calcium silicate, sodium aluminate, calcium aluminate, sodium aluminosilicate, magnesium silicate, glass balloon, carbon Examples thereof include black, zinc oxide, antimony trioxide, zeolite, hydrotalcite, metal fiber, metal whisker, ceramic whisker, potassium titanate, boron nitride, graphite, and carbon fiber.
  • nucleating agents include sorbitol compounds and metal salts thereof; benzoic acid and metal salts thereof; phosphoric acid ester metal salts; ethylene bisoleic acid amide, methylene bisacrylic acid amide, ethylene bisacrylic acid amide, hexamethylene bis-9,10 -Dihydroxystearic acid bisamide, p-xylylene bis-9,10-dihydroxystearic acid amide, decanedicarboxylic acid dibenzoyl hydrazide, hexanedicarboxylic acid dibenzoyl hydrazide, 1,4-cyclohexanedicarboxylic acid dicyclohexylamide, 2,6-naphthalenedicarboxylic acid Dianilide, N, N ′, N ′′ -tricyclohexyltrimesic acid amide, trimesic acid tris (t-butylamide), 1,4-cyclohexanedicarboxylic acid dianilide, 2,
  • the content in the case of using these “other components” in the release layer in the present invention is not limited, but is usually 0.01% by weight or more, preferably 0.2% in the release layer or the resin composition described later. It is desirable that the content is not less than 10% by weight, usually not more than 10% by weight, preferably not more than 5% by weight.
  • These other components have a concentration of 2 to 50 times, preferably 3 to 30 times the above-described content when used as a masterbatch in the case where the raw material used for the release layer is preliminarily used as a resin composition. It can also be contained.
  • the resin composition of the present invention is a resin composition containing a polyolefin resin (A), a fatty acid bisamide compound (B), and optionally other components.
  • the release layer in the present invention is a layer containing a polyolefin resin (A), a fatty acid bisamide compound (B), and optionally other components.
  • the fatty acid bisamide compound (B) is added to 100 parts by weight of the polyolefin resin (A). Usually 0.5 parts by weight or more, preferably 1 part by weight or more, more preferably 2 parts by weight or more, while usually 20 parts by weight or less, preferably 15 parts by weight or less, more preferably 10 parts by weight or less. .
  • the content rate of a fatty acid bisamide compound (B) is less than the said lower limit, there exists a tendency for the mold release property and its uniformity at the time of setting it as a mold release film to fall.
  • the content ratio of the fatty acid bisamide compound (B) exceeds the upper limit, the excess fatty acid bisamide compound leaks from the release layer and is transferred to the adhesive layer side, or the release film mechanically. The strength may decrease.
  • the content ratio of the fatty acid bisamide compound (B) in the resin composition or the release layer is not limited, but is usually 0.5 parts by weight or more, preferably 1 part by weight or more, more preferably 2 parts by weight or more, The content is usually 20 parts by weight or less, preferably 15 parts by weight or less, more preferably 10 parts by weight or less.
  • the content rate of a fatty acid bisamide compound (B) is less than the said lower limit, there exists a tendency for the mold release property and its uniformity at the time of setting it as a mold release film to fall.
  • the content ratio of the fatty acid bisamide compound (B) exceeds the upper limit, the excess fatty acid bisamide compound leaks from the release layer and is transferred to the adhesive layer side, or the release film mechanically. The strength may decrease.
  • the release layer in the present invention can be obtained by blending the above-mentioned components as raw materials and molding as it is to obtain a molded body. However, these are previously set as the resin composition of the present invention, and the resin composition is molded. It is preferable to produce a molded product obtained in this manner and use this as a release layer.
  • the resin composition of the present invention can be obtained by mixing the above-described components at a predetermined ratio.
  • the mixing method is not particularly limited as long as the raw material components can be uniformly dispersed and mixed. That is, a composition in which each component is uniformly distributed can be obtained by mixing the above-described raw material components simultaneously or in any order.
  • the raw material components of the resin composition may be mixed in an arbitrary order and then heated, or may be mixed while sequentially melting all the raw material components. Furthermore, only a part of the above-described components may be left as a resin composition, and the resin composition and other components may be blended and used for forming a release layer.
  • the mixing method and mixing conditions are not particularly limited as long as each raw material component is uniformly mixed, but from the viewpoint of productivity, the raw materials are mixed using, for example, a tumbler blender, V blender, ribbon blender, Henschel mixer, etc.
  • a melt kneading method using a continuous kneader such as a single screw extruder or a twin screw extruder and a batch kneader such as a mill roll, a Banbury mixer, or a pressure kneader is preferable.
  • the temperature at the time of melt mixing may be a temperature at which at least one of the raw material components is in a molten state, but usually a temperature at which all the components used are melted is selected, and generally it is carried out at 150 to 250 ° C.
  • the melt flow rate (MFR) of the resin composition of the present invention is not particularly limited, but is usually 0.5 to 200 g / 10 minutes, preferably 1 to 50 g under the conditions of 230 ° C. and a load of 2.16 kg (21.18 N). / 10 minutes, more preferably 2 to 25 g / 10 minutes. If the MFR is less than the lower limit, molding at high speed may be difficult. Moreover, when MFR exceeds the said upper limit, the mechanical strength of the mold release layer obtained by shape
  • the release film of the present invention may be a single-layer film obtained by molding only the release layer alone, as long as it has the release layer, or a layer other than the release layer (hereinafter referred to as other layers). May be referred to as a layer).
  • the other layers include a base layer (support layer) such as other resin, metal, and glass, a protective layer, and a coating layer, in addition to the adhesive layer described later. Since the release film of the present invention is excellent in releasability, the effect can be remarkably exhibited by using it as a laminate having a release layer and other layers.
  • the layer structure of the laminate is arbitrary, and the other layer may have a plurality of the same or different layers, or may have two or more release layers.
  • the shape of the release film of the present invention is not limited, and is usually a flat shape of a single sheet or a roll shape obtained by winding a flat film, but may be a cylindrical shape or an indefinite shape.
  • the method for producing the release film of the present invention is not particularly limited, but melt extrusion is preferred.
  • melt extrusion molding a release film can be obtained by extruding a raw material from an extruder into a film or sheet.
  • the melt extrusion molding includes inflation molding and blow molding.
  • a release film can be manufactured by a molding method such as injection molding or press molding. Further, the release film obtained by these molding methods may be subjected to stretching treatment such as uniaxial or biaxial.
  • the release film as the laminate is preferably manufactured by coextrusion molding, extrusion lamination molding, extrusion coating, or the like in terms of manufacturing efficiency.
  • at least one base layer is usually used. That is, it is a method of unwinding an already formed base material layer, laminating a molten resin or the like on the surface of the base material layer, or coating and drying a solution.
  • the release layer can be used as a base material layer, and other layers can be used as the base material layer.
  • the raw material of the release layer in the present invention and the raw material resin constituting the other layer are extruded from different extruders and laminated in a die for molding. Since the release layer in the present invention has good releasability, an appropriate laminate release film can be obtained even by coextrusion molding by appropriately selecting a resin or the like to be used as another layer. In addition, it can also be set as the laminated body of a 3 or more layer structure by coextrusion molding.
  • the release film of the present invention has a good release property of the release layer, the above problems do not occur.
  • the fatty acid bisamide compound (B) has a specific aliphatic group, so that it forms a stable crystal structure, and the polyolefin resin (A) has a specific bending elastic modulus. It is thought that it originates in having favorable affinity with a compound (B). By this, it is thought that a fatty acid bisamide compound (B) transfers to another layer, and, thereby, it is possible to obtain a release film having good release properties even by coextrusion molding.
  • release film of the present invention "single-layer release film” consisting only of the release layer, “double-sided adhesive tape with release film” having a release layer on one or both sides of the adhesive layer, “Single-sided adhesive tape with release film” in which base layer and adhesive layer are integrated, and release layer is laminated on the adhesive layer side, “single-sided adhesive tape” in which release layer and adhesive layer are integrated Can be mentioned.
  • a function of the release layer when storing the adhesive layer in a non-use state, etc., a function to protect the adhesive surface so that other substances do not adhere, a shielding function to prevent the adhesive layers from sticking to each other, It has a function of preventing the adhesive component from leaking out, and can be easily peeled off from the adhesive layer, and it should not cause a decrease in adhesive force due to the release agent component remaining in the adhesive layer. .
  • the release film of the present invention has the above properties at a high level because the release force of the release layer is uniform. Furthermore, even when a wide release film is formed, the release performance in the width direction of the sheet can be made uniform. For this reason, even when it is set as the release film of a large area, uniform adhesiveness and mold release property can be exhibited. Further, even when a plurality of thin release films (tapes) are manufactured by slit cutting a wide release film, the adhesiveness and release properties between lots can be kept uniform.
  • the thickness of the release film of the present invention is not particularly limited, but the thickness of the release layer in the single-layer release film or laminate is usually 0.1 to 100 ⁇ m, preferably 0.5 to 100 ⁇ m. When the thickness is in the above range, there is no deterioration in the mold release performance due to non-uniform thickness, and it is economically preferable.
  • the total thickness when the release film of the present invention is a laminate is not particularly limited, but is usually 0.5 ⁇ m to 5 mm, preferably 1 ⁇ m to 2 mm, more preferably 10 ⁇ m to 1 mm.
  • the pressure-sensitive adhesive layer constituting the release film as the laminate is not limited as long as it has a pressure-sensitive adhesive performance to other substances. Further, in the present invention, not only when the pressure-sensitive adhesive layer is independently provided, but also when the pressure-sensitive adhesive layer functions as a pressure-sensitive adhesive layer by applying or impregnating the surface of the release layer or the base material layer, for example. Included in the adhesive layer.
  • a base material layer may be a porous material or a fibrous material such as a nonwoven fabric.
  • Examples of the material used for the adhesive layer in the present invention include amorphous or low crystalline resins having a glass transition temperature of 23 ° C. or lower, thermoplastic elastomers, various oligomers having a number average molecular weight of 500 to 10,000, and the like. Or a mixture thereof. Further, a crosslinked or non-crosslinked resin may be used by dissolving or swelling with a low-volatile solvent.
  • Specific examples of the material for the adhesive layer include thermoplastic elastomers such as styrene thermoplastic elastomer, olefin thermoplastic elastomer, polyester thermoplastic elastomer, acrylic adhesive, natural rubber adhesive, and synthetic rubber adhesive. Examples thereof include an adhesive and a silicone-based adhesive. Among these, it is preferable to use a styrene thermoplastic elastomer or a silicone pressure sensitive adhesive. These may be used alone or in combination of two or more.
  • the styrenic thermoplastic elastomer examples include a block copolymer having a polymer block mainly composed of a vinyl aromatic compound and a polymer block imparting flexibility. Specifically, it is obtained by hydrogenating a block copolymer having a polymer block mainly composed of a vinyl aromatic compound and a polymer block mainly composed of butadiene and / or isoprene and / or the block copolymer. Examples thereof include hydrogenated block copolymers.
  • the vinyl aromatic compound is not limited, but styrene derivatives such as styrene and ⁇ -methylstyrene are preferable.
  • thermoplastic elastomer examples include copolymers having monomer components such as ethylene, propylene, ⁇ -olefins having about 4 to 10 carbon atoms, non-conjugated dienes, vinyl acetate, and the like.
  • a copolymer of ethylene and propylene a copolymer of ethylene and an ⁇ -olefin having about 4 to 10 carbon atoms, a copolymer of propylene and an ⁇ -olefin having about 4 to 10 carbon atoms, Copolymers of ethylene and non-conjugated diene components, copolymers of ethylene and ⁇ -olefins having about 3 to 10 carbon atoms and non-conjugated diene components, blends of olefin resins such as polypropylene and olefin rubber, etc. Is mentioned. These may be any of a block copolymer, a graft copolymer, and a random copolymer.
  • the olefinic thermoplastic elastomer may be cross-linked.
  • Examples of the ⁇ -olefin include 1-butene, 3-methyl-1-butene, 1-pentene, 4-methyl-1-pentene, 1-hexene, 1-octene and 1-decene.
  • Examples of the non-conjugated diene include 1,4-hexadiene, 1,6-octadiene, 2-methyl-1,5-hexadiene, 6-methyl-1,5-heptadiene, and 7-methyl-1,6-octadiene.
  • Chain non-conjugated dienes cyclohexadiene, dicyclopentadiene, methyltetrahydroindene, 5-vinylnorbornene, 5-ethylidene-2-norbornene, 5-methylene-2-norbornene, 5-isopropylidene-2-norbornene, 6- And cyclic non-conjugated dienes such as chloromethyl-5-isopropenyl-2-norbornene.
  • polyester-based thermoplastic elastomer examples include block copolymers of crystalline polyester and polyalkylene ether or aliphatic polyester.
  • crystalline polyester block include aromatic polyesters such as polybutylene terephthalate, and alicyclic polyesters such as polyester obtained by condensation from cyclohexanedicarboxylic acid and cyclohexanedimethanol.
  • polyalkylene ether block examples include polytetramethylene ether glycol, polytrimethylene ether glycol, polypropylene ether glycol, and polyethylene ether glycol.
  • the aliphatic polyester is condensed from an aliphatic dicarboxylic acid having about 2 to 10 carbon atoms such as adipic acid or sebacic acid and an aliphatic diol having about 2 to 10 carbon atoms such as ethylene glycol or 1,4-butanediol.
  • an aliphatic dicarboxylic acid having about 2 to 10 carbon atoms such as adipic acid or sebacic acid
  • an aliphatic diol having about 2 to 10 carbon atoms such as ethylene glycol or 1,4-butanediol.
  • the pressure-sensitive adhesive layer used in the present invention may similarly contain the other components that may be contained in the release layer.
  • the adhesive layer may preferably contain a hydrocarbon rubber softener.
  • a hydrocarbon rubber softener is preferably a mineral oil or synthetic resin softener, more preferably a mineral oil softener.
  • Mineral oil softeners are generally a mixture of aromatic hydrocarbons, naphthenic hydrocarbons and paraffinic hydrocarbons, with paraffinic oils in which 50% or more of all carbon atoms are paraffinic hydrocarbons, About 30-45% or more of all carbon atoms are called naphthenic oils, and about 35% or more of all carbon atoms are aromatic hydrocarbons are called carbon atom aromatic oils. ing. Of these, paraffinic oil is preferred because of its good hue.
  • the synthetic resin softener include polybutene and low molecular weight polybutadiene.
  • the hydrocarbon rubber softener may be any one of the above-mentioned various softeners or a mixture of plural kinds.
  • the kinematic viscosity at 40 ° C. of the hydrocarbon rubber softener is preferably 20 centistokes or more, more preferably 50 centistokes or more, while it is preferably 800 centistokes or less, 600 centistokes. It is preferably less than or equal to Stokes.
  • the flash point (COC method) of the hydrocarbon rubber softener is not limited, but is preferably 200 ° C. or higher, and more preferably 250 ° C. or higher.
  • a tackifier for example, petroleum-based resins such as aliphatic / aromatic copolymer systems and alicyclic systems, coumarone-indene resins, terpene resins, terpene phenols, etc.
  • resins, alkylphenol resins, rosin resins, xylene resins, and hydrides thereof can be appropriately selected and used.
  • the tackifier used in the present invention may be composed mainly of these tackifiers.
  • the release film of the present invention is not limited, it can be suitably used as a release film for protecting the surface of various products (hereinafter sometimes referred to as a surface protective film).
  • a surface protective film the layer structure in the case of using as a surface protective film is not limited, the single-sided adhesive tape with a release film or a single-sided adhesive tape is suitable among the above-mentioned aspects of a release film. That is, the base material layer and the adhesive layer are integrated, and the release layer is peeled off from the “single-sided adhesive tape with a release film” in which the release layer is laminated on the adhesive layer side.
  • the adhesive layer of the “single-sided adhesive tape” in which the release layer and the adhesive layer are integrated may be attached to an object for surface protection.
  • the material of the object to be surface-protected is not limited, and examples thereof include resin, metal, glass, and other inorganic substances. Further, the object may be one whose surface is painted or chemically or physically treated. Although the use of the target object which protects a surface is not limited, A building member, a motor vehicle member, a display member, daily necessities, etc. are mentioned. As a building member, an exterior member, an interior member, a bathtub, a kitchen member etc. are mentioned, for example. Examples of the automobile member include a bonnet, a door panel, a bumper, a dash panel, a window, and a roof. Examples of the display member include a polarizing plate, a retardation plate, and an exterior of an OA device.
  • the release film of the present invention is used as a surface protective film for these various products, it maintains good adhesiveness during product protection, and when released from the product, the release film or release agent is the product. It can be peeled off from the product with a stable release force. Furthermore, even when a product to which the release film of the present invention is attached is held in a high temperature environment, good release performance and adhesive performance can be exhibited.
  • A-4 Tuffmer P0480 (MFR (230 ° C., 2.16 kg) 1.8 g / 10 min, flexural modulus 20 MPa, ethylene / propylene copolymer) manufactured by Mitsui Chemicals, Inc.
  • A-5 Nippon Polypro Co., Ltd., Novatec PP MA3 (MFR (230 ° C., 2.16 kg) 11 g / 10 min, flexural modulus 1500 MPa, propylene homopolymer)
  • A-6 Novatec PP FW4B manufactured by Nippon Polypro Co., Ltd.
  • A-7 Novatec PP EG7F manufactured by Nippon Polypro Co., Ltd. (MFR (230 ° C., 2.16 kg) 1.3 g / 10 min, flexural modulus 1050 MPa, propylene / ethylene copolymer)
  • A-8 Tuffmer A4085S manufactured by Mitsui Chemicals, Inc. (MFR (230 ° C., 2.16 kg) 3.4 g / 10 min, flexural modulus 70 MPa, ethylene / butene copolymer)
  • ⁇ Release agent> B-1 Behenic acid bisamide 115.6 parts of behenic acid (C 21 H 43 COOH, Tokyo Chemical Industry Co., Ltd., purity 95% or more) were melted at 140 ° C. in a nitrogen atmosphere, and ethylenediamine (Wako Pure Chemical Industries, Ltd.) was melted there. 10 parts) (purity 99% or more). After the addition, the mixture was heated to 160 ° C. and reacted for 6 hours. Moisture generated during the reaction was separated and removed using a Dean-Stark tube. After the reaction, after cooling to room temperature, 1320 parts of xylene was added, heated to 160 ° C. and stirred for 1 hour to dissolve.
  • fatty acid bisamide (B-1) mainly composed of behenic acid bisamide.
  • B-2 Armoslip E (erucic acid amide) manufactured by Lion Corporation B-3 (for comparative example): Alfro AD-281F (ethylene bisoleic acid amide) manufactured by NOF Corporation
  • B-4 for comparative example: Sripax E (ethylene bis stearic acid amide) manufactured by Nippon Kasei Co., Ltd.
  • -Adhesive tape 1 Commercially available silicone adhesive tape with a width of 25 mm (Nitto Denko Corporation, No. 903UL)
  • -Adhesive tape 2 Acrylic adhesive tapes cut to a width of 25 mm (Nitto Denko Corporation, No. 31B)
  • -Adhesive tape 3 Using a three-layer, three-layer T-die film molding machine manufactured by Plako, with the molding temperature of 220 ° C and the take-up speed of 10 m / min, the outer layer / intermediate layer / adhesive layer from the cooling roll side. A laminate having a thickness of 10 ⁇ m, 35 ⁇ m, and 5 ⁇ m was obtained. The outer layer and the intermediate layer are the same resin and are regarded as a single layer having a thickness of 45 ⁇ m. The obtained laminate was cut as an adhesive tape having a width of 25 mm in the extrusion direction to obtain an adhesive tape. Resins used for the outer layer / intermediate layer and the adhesive layer are as follows.
  • Example 1 6 parts by weight of B-1 is blended with 100 parts by weight of A-1, and melt-kneaded at 230 ° C. in an extruder (manufactured by Nippon Steel Works, TEX30 twin screw extruder) to form pellets of a resin composition Got. Using the pellets of this resin composition as a release layer, using the above-mentioned Nippon Polypro Co., Ltd., Novatec PP FY4 as a raw material for the support layer, Plako Co., Ltd., a multilayer T-die coextrusion molding machine with a thickness of 50 ⁇ m : 10 ⁇ m, support layer: 40 ⁇ m), and a laminate (release film) having a width of 25 cm was formed. Evaluation 1 of the following mold release performance was performed using the obtained laminated body (release film). The results are shown in Table 1.
  • ⁇ Evaluation 1> The laminate (release film) produced above is cut into a rectangle with a width of 30 mm in the extrusion direction (MD direction), and the adhesive tape 1, the adhesive tape 2, and the adhesive tape 3 on the release layer side surface. After any of the pressure-sensitive adhesive surfaces were put together, a rubber roller having a weight of 2 kg was reciprocated once and pressure-bonded to obtain a test piece for evaluation. After leaving the test piece for evaluation at room temperature for 1 hour, the force required to peel the interface between the release layer and the adhesive layer in the 180 ° direction at a tensile speed of 300 mm / min (average value of 5 samples) is measured. This was defined as “release force (N / cm)”.
  • test specimens for evaluation cut to a width of 30 mm were sampled at seven locations in the width direction from one end to the other end of a 25 cm wide laminate (release film), and (1) to (7), respectively. They were numbered, and the respective release forces were measured ((1) and (7) are the end portions of the sheet, and (4) is the central portion of the sheet width).
  • the average value was measured five times, and the maximum value and the minimum value of the release force in the test specimens of (1) to (7) were confirmed. It is preferable that the value of the releasing force is small and the difference between the maximum value and the minimum value is small.
  • Examples 2 to 9 Comparative Examples 1 to 9> Except that the type of the propylene polymer and the blending amount of the release agent were as shown in Table 1, pellets of the resin composition were produced in the same manner as in Example 1, and the laminate (release agent) was obtained in the same manner as in Example 1. Mold film). Evaluation 1 of release performance was performed in the same manner as Example 1 using the obtained laminate (release film). The results are shown in Table 1.
  • the release force was uniform in any case where the amount of the release agent was changed, and no difference depending on the position of the sheet was observed.
  • a comparative example using a propylene polymer having a high flexural modulus as a raw material there was a difference in the release force depending on the position of the laminate (release film). This difference in performance becomes more prominent when a wider-width laminate (release film) is produced.
  • Examples 10 to 16 Comparative Examples 10 to 20> Except that the type and amount of the release agent are as shown in Table 2, pellets of the resin composition were produced in the same manner as in Example 1, and a laminate (release film) was formed in the same manner as in Example 1. did. Using the obtained laminate (release film), the following evaluation performance evaluation 2 and evaluation 3 were performed. The results of evaluation 2 are shown in Table 2, and the results of evaluation 3 are shown in Table 3.
  • the raw material blend compositions of Examples 10 to 16 are the same as those of Examples 1 to 6 and 8, respectively.
  • This value corresponds to the release force of the evaluation test piece (4) in Evaluation 1. This value is preferably small.
  • the adhesive layer side of the peeled evaluation test piece is attached to the upper surface of a stainless steel (SUS) plate (the adhesive surface of the adhesive tape is attached to the stainless steel plate), and a rubber roller weighing 2 kg is made to reciprocate once. And crimped. After standing at room temperature for 1 hour, the force (average value of 5 samples) required to peel the interface between the stainless steel plate and the adhesive tape in the 180 ° direction at a tensile speed of 300 mm / min was measured. (N / cm) ". A large value is preferable.
  • heating release force (N / cm) This was defined as “heating release force (N / cm)”. This value is preferably small.
  • the adhesive layer side of the peeled evaluation test piece is attached to the upper surface of a stainless steel (SUS) plate (the adhesive surface of the adhesive tape is attached to the stainless steel plate), and a rubber roller weighing 2 kg is made to reciprocate once. And crimped. After leaving at room temperature for 1 hour, the force (average value of 5 samples) required to peel the interface between the stainless steel plate and the adhesive tape in the 180 ° direction at a tensile speed of 300 mm / min was measured. Force (N / cm) ". A large value is preferable.
  • the release property is good in any case where the compounding amount of the release agent is changed, and the adhesive layer and the release layer are bonded together. Even when stored in a high temperature environment, the variation in peel force was small and the adhesive performance of the abutting adhesive tape was excellent. On the other hand, in comparative examples that do not use a release agent and in comparative examples that use a release agent different from the general formula (1) as a raw material, the releasability is poor and the adhesive layer and the release layer are bonded together. It was confirmed that the peel force fluctuated greatly when stored in a high temperature environment.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Laminated Bodies (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Adhesive Tapes (AREA)

Abstract

L'objet de la présente invention réside dans un film antiadhésif et dans une composition de résine qui présentent une performance antiadhésive uniforme et modérée, qui sont également avantageux en termes de ré-adhérence d'une couche adhésive et qui présentent une performance de déroulement de rouleau avantageuse également lors de la coextrusion. La présente invention réside dans une composition de résine contenant une résine (A) polyoléfinique présentant un module de flexion d'au moins 800 MPa et un composé (B) de bisamide d'acide gras représenté par la formule générale (1), et réside également dans un film antiadhésif présentant une couche antiadhésive contenant la composition de résine. R-CONH-(CH2)n-NHCO-R (1) (dans la formule, n représente un entier de 1 à 6, et chaque R représente indépendamment un groupe aliphatique en C19 ou supérieur).
PCT/JP2012/067746 2011-07-12 2012-07-11 Composition de résine et film antiadhésif Ceased WO2013008861A1 (fr)

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KR1020147000467A KR20140038509A (ko) 2011-07-12 2012-07-11 수지 조성물 및 이형 필름
CN201280034091.XA CN103649204A (zh) 2011-07-12 2012-07-11 树脂组合物和离型膜

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TWI568782B (zh) 2017-02-01
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KR20140038509A (ko) 2014-03-28
CN103649204A (zh) 2014-03-19
JP2013227472A (ja) 2013-11-07

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