WO2021193884A1 - Transparentizing agent, resin composition containing same, molded article of said resin composition, and method for producing resin composition - Google Patents

Transparentizing agent, resin composition containing same, molded article of said resin composition, and method for producing resin composition Download PDF

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WO2021193884A1
WO2021193884A1 PCT/JP2021/012752 JP2021012752W WO2021193884A1 WO 2021193884 A1 WO2021193884 A1 WO 2021193884A1 JP 2021012752 W JP2021012752 W JP 2021012752W WO 2021193884 A1 WO2021193884 A1 WO 2021193884A1
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carbon atoms
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福井 聡
直人 上田
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株式会社Adeka
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D251/00Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/26Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
    • C07D251/30Only oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/15Heterocyclic compounds having oxygen in the ring
    • C08K5/156Heterocyclic compounds having oxygen in the ring having two oxygen atoms in the ring
    • C08K5/1575Six-membered rings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/34Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3477Six-membered rings
    • C08K5/3492Triazines
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions 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
    • C08L23/10Homopolymers or copolymers of propene
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00Materials not provided for elsewhere

Definitions

  • the present invention relates to a clearing agent, a resin composition containing the same, a molded product thereof, and a method for producing the resin composition.
  • the present invention relates to a resin composition containing, a molded product thereof, and a method for producing the resin composition.
  • Polyolefin-based resins such as polypropylene are excellent in molding processability, heat resistance, mechanical properties, etc., and have a small specific gravity, and are widely used for films, sheets, and various molded products (structural parts, etc.). There is. However, depending on the use of the molded product, the molded product made of a polyolefin resin may not be said to have sufficiently excellent transparency.
  • Patent Document 1 proposes a clearing agent containing an aromatic phosphoric acid ester metal salt and an acetal compound.
  • an object of the present invention is to provide a clearing agent capable of imparting excellent transparency to a molded product, a resin composition containing the transparent agent, a molded product thereof, and a method for producing the resin composition.
  • the clearing agent of the present invention has (A) the following general formula (1), (In the general formula (1), Ar 1 , Ar 2 and Ar 3 each independently represent an unsubstituted phenyl group or a phenyl group having a substituent), and (B) the following General formula (2), (In the general formula (2), R 1 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. R 2 , R 3 , R 4 and R 5 are independent hydrogen atoms, halogen atoms and cyano groups, respectively.
  • X represents a single bond, an acetal compound represented by -CH (OH) -group or -CH (OH) CH (OH) -group.
  • the ratio (A) / (B) of the content (parts by mass) of the (A) triazine compound to the content (parts by mass) of the (B) acetal compound is 1/99 to 99/1. It is characterized by.
  • At least one of Ar 1 , Ar 2 and Ar 3 of the general formula (1) has a substituent containing a carbonyl group.
  • R 1 , R 2 , R 3 , R 4 and R 5 in the general formula (2) are independently hydrogen atoms or alkyl groups having 1 to 4 carbon atoms, respectively. Yes, and it is preferable that X is a -CH (OH) -group.
  • the resin composition of the present invention comprises a polyolefin resin and (A) the following general formula (1), (In the general formula (1), Ar 1 , Ar 2 and Ar 3 each independently represent an unsubstituted phenyl group or a phenyl group having a substituent), and (B) the following General formula (2), (In the general formula (2), R 1 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. R 2 , R 3 , R 4 and R 5 are independent hydrogen atoms, halogen atoms and cyano groups, respectively.
  • X represents a single bond, an acetal compound represented by -CH (OH) -group or -CH (OH) CH (OH) -group.
  • the ratio (A) / (B) of the content (parts by mass) of the (A) triazine compound to the content (parts by mass) of the (B) acetal compound is 1/99 to 99/1.
  • the total content of the (A) triazine compound and the (B) acetal compound with respect to 100 parts by mass of the polyolefin-based resin is 0.001 to 10 parts by mass.
  • the polyolefin-based resin is preferably a polypropylene-based resin.
  • the molded product of the present invention is characterized by being obtained by molding the resin composition of the present invention.
  • a container is preferable as the molded product of the present invention.
  • the method for producing the resin composition of the present invention is to use a polyolefin resin according to (A) the following general formula (1).
  • Ar 1 , Ar 2 and Ar 3 each independently represent an unsubstituted phenyl group or a phenyl group having a substituent
  • B the following General formula (2)
  • R 1 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms.
  • R 2 , R 3 , R 4 and R 5 are independent hydrogen atoms, halogen atoms and cyano groups, respectively.
  • X represents a single bond, an acetal compound represented by -CH (OH) -group or -CH (OH) CH (OH) -group.
  • the ratio (A) / (B) of the blending amount (parts by mass) of the (A) triazine compound to the blending amount (parts by mass) of the (B) acetal compound is 1/99 to 99 /.
  • the total amount of the (A) triazine compound and the (B) acetal compound is 0.001 to 10 parts by mass with respect to 100 parts by mass of the polyolefin resin.
  • One preferred embodiment of the method for producing a resin composition of the present invention is a polyolefin resin and (A) the following general formula (1).
  • Ar 1 , Ar 2 and Ar 3 each independently represent an unsubstituted phenyl group or a phenyl group having a substituent.
  • R 1 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms.
  • R 2 , R 3 , R 4 and R 5 are independent hydrogen atoms, halogen atoms and cyano groups, respectively.
  • X represents a single bond, -CH (OH) -group or -CH (OH) CH (OH) -group).
  • the ratio (A) / (B) of the compounding amount (parts by mass) of the (A) triazine compound to the compounding amount (parts by mass) of the (B) acetal compound is 1/99 to 99/1.
  • the total amount of the (A) triazine compound and the (B) acetal compound is 0.001 to 10 parts by mass with respect to 100 parts by mass of the polyolefin resin.
  • R 1 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms.
  • R 2 , R 3 , R 4 and R 5 are independent hydrogen atoms, halogen atoms and cyano groups, respectively.
  • X represents a single bond, an acetal compound represented by -CH (OH) -group or -CH (OH) CH (OH) -group.
  • Ar 1 , Ar 2 and Ar 3 each independently represent an unsubstituted phenyl group or a phenyl group having a substituent.
  • the ratio (A) / (B) of the compounding amount (parts by mass) of the (A) triazine compound to the compounding amount (parts by mass) of the (B) acetal compound is 1/99 to 99/1.
  • the total amount of the (A) triazine compound and the (B) acetal compound to be blended with respect to 100 parts by mass of the polyolefin resin is 0.001 to 10 parts by mass.
  • the present invention it is possible to provide a transparent agent capable of imparting excellent transparency to a molded product, a resin composition containing the transparent agent, a molded product thereof, and a method for producing the resin composition.
  • the clearing agent of the present embodiment includes (A) a triazine compound represented by the following general formula (1) and (B) an acetal compound represented by the following general formula (2).
  • the ratio (A) / (B) of the content (parts by mass) of the (A) triazine compound to the content (parts by mass) of the (B) acetal compound is 1/99 to 99/1.
  • Ar 1 , Ar 2 and Ar 3 each independently represent an unsubstituted phenyl group or a phenyl group having a substituent
  • R 1 is hydrogen.
  • R 2 , R 3 , R 4 and R 5 independently represent a hydrogen atom, a halogen atom, a cyano group, an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, or R 2 and R 3 or R 4 and R 5 are linked to each other to represent an alkylene group having 3 to 6 carbon atoms or an alkylene dioxy group having 1 to 4 carbon atoms.
  • X represents a single bond, -CH (OH) -group or -CH (OH) CH (OH) -group.
  • Examples of the substituents of Ar 1 , Ar 2 and Ar 3 of the general formula (1) include a halogen atom, a hydroxy group, a carboxy group, and an alkyl group having 1 to 20 carbon atoms which may have a substituent.
  • An aryl group having 6 to 20 carbon atoms which may have a substituent, an amino group which may have a substituent, an aminocarbonyl group which may have a substituent also referred to as a carbamoyl group
  • alkylthio groups having 1 to 20 carbon atoms which may have a substituent
  • alkylcarbonyl groups having 2 to 20 carbon atoms which may have a substituent
  • substituents It may have an arylcarbonyl group having 7 to 20 carbon atoms, an alkylcarbonyloxy group having 2 to 20 carbon atoms which may have a substituent, and a carbon atom which may have a substituent.
  • arylcarbonyloxy groups alkoxycarbonyl groups having 2 to 20 carbon atoms which may have a substituent, aryloxycarbonyl groups having 7 to 20 carbon atoms which may have a substituent, An aminocarbonyl group which may have a substituent, an alkylcarbonylamino group which may have a substituent and has 2 to 20 carbon atoms, and an alkylcarbonylamino group which may have a substituent and which has 7 to 20 carbon atoms. Examples thereof include an arylcarbonylamino group and a heterocyclic group having 2 to 20 carbon atoms which may have a substituent.
  • the carboxy group and the sulfo group may form a salt.
  • the substituents of Ar 1 , Ar 2 and Ar 3 include, for example, methyl, ethyl, propyl, isopropyl, cyclopropyl, butyl, sec-butyl, and the like.
  • tert-butyl isobutyl, amyl, isoamyl, tert-amyl, cyclopentyl, hexyl, 2-hexyl, 3-hexyl, cyclohexyl, bicyclohexyl, 1-methylcyclohexyl, heptyl, 2-heptyl, 3-heptyl, isoheptyl, tert- Alkyl groups such as heptyl, n-octyl, isooctyl, tert-octyl, 2-ethylhexyl, nonyl, isononyl, decyl, vinyl, 1-methylethenyl, 2-methylethenyl, 2-propenyl, 1-methyl-3-propenyl, 3- Butenyl, 1-methyl-3-butenyl, isobutenyl, 3-pentenyl, 4-hexenyl, cyclohexenyl, bicyclo
  • halogen atoms of the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include fluorine, chlorine, bromine and iodine.
  • the alkyl groups having 1 to 20 carbon atoms which may have a substituent include methyl, ethyl and n-propyl. Isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, tert-amyl, 1,2-dimethylpropyl, n-hexyl, cyclohexyl, 1,3-dimethylbutyl, 1- Isopropylpropyl, 1,2-dimethylbutyl, n-heptyl, 2-heptyl, 1,4-dimethylpentyl, tert-heptyl, 2-methyl-1-isopropylpropyl, 1-ethyl-3-methylbutyl, n-octyl, tert-octyl, 2-methyl-1-isopropylpropyl, 1-ethyl-3-
  • the aryl groups having 6 to 20 carbon atoms which may have a substituent include phenyl, p-methylphenyl and o-. Methylphenyl, p-tert-butylphenyl, p-methoxyphenyl, p-chlorophenyl, p-nitrophenyl, p-cyanophenyl, o-biphenylyl, m-biphenylyl, p-biphenylyl, ⁇ -naphthyl, ⁇ -naphthyl, Examples thereof include 1-anthryl, 2-anthryl, 9-anthryl, 1-phenyl, 2-phenyl, 3-phenyl, 4-phenyl, 9-phenyl and the like.
  • amino groups that may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include the above-mentioned alkyl group or the above-mentioned alkyl group in addition to the unsubstituted amino group.
  • amino groups substituted with the above aryl groups include amino, methylamino, ethylamino, n-propylamino, isopropylamino, cyclopropylamino, n-butylamino, isobutylamino, and sec-butylamino.
  • aminocarbonyl group which may have a substituent of the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1), in addition to the unsubstituted aminocarbonyl group, the above alkyl group or the above.
  • aminocarbonyl groups substituted with aryl groups and specific examples thereof include aminocarbonyl, methylaminocarbonyl, ethylaminocarbonyl, n-propylaminocarbonyl, isopropylaminocarbonyl, n-butylaminocarbonyl, isobutylaminocarbonyl, sec.
  • Examples of the alkoxy group having 1 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include methoxy, ethoxy, and n-propoxy. Isopropoxy, n-butoxy, isobutoxy, sec-butoxy, tert-butoxy, n-pentyloxy, isopentyloxy, neopentyloxy, 1,2-dimethyl-propoxy, n-hexyloxy, cyclohexyloxy, 1,3- Examples thereof include dimethylbutoxy and 1-isopropylpropoxy.
  • the aryloxy groups having 6 to 20 carbon atoms which may have a substituent include phenoxy, naphthyloxy and p-. Methylphenoxy, o-methylphenoxy, p-tert-butylphenoxy, p-methoxyphenoxy, p-chlorpheninoxy, p-nitrophenoxy, p-cyanophenoxy, o-biphenylyloxy, m-biphenylyloxy, p -Biphenylyloxy, ⁇ -naphthyloxy, ⁇ -naphthyloxy, 1-anthryloxy, 2-antryloxy, 9-antryloxy, 1-phenanthryloxy, 2-phenanthryloxy, 3-fe Examples thereof include nantriloxy, 4-phenanthryloxy, 9-phenanthryloxy and the like.
  • alkylthio group having 1 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include methylthio group, ethylthio group and n-.
  • examples thereof include a propylthio group, an isopropylthio group, an n-butylthio group, an isobutylthio group, a sec-butylthio group, a tert-butylthio group and the like.
  • the alkylcarbonyl group having 2 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) is methylcarbonyl (also referred to as acetyl).
  • Examples of the arylcarbonyl group having 7 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include benzoyl and p-methylbenzoyl. p-tert-butylbenzoyl, p-methoxybenzoyl, p-chlorbenzoyl, p-nitrobenzoyl, p-cyanobenzoyl, o-biphenylylcarbonyl, m-biphenylylcarbonyl, p-biphenylylcarbonyl, ⁇ -naphthylcarbonyl, ⁇ -naphthylcarbonyl, 1-anthrylcarbonyl, 2-anthrylcarbonyl, 9-anthrylcarbonyl, 1-phenanthrylcarbonyl, 2-phenanthrylcarbonyl, 3-phenanthrylcarbonyl, 4-phenanthrylcarbonyl , 9-Phenantril carbonyl and
  • alkylcarbonyloxy group having 2 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) are methylcarbonyloxy and ethylcarbonyl.
  • Benzoyloxy and p-methyl are examples of arylcarbonyloxy groups having 7 to 20 carbon atoms which may have substituents among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1).
  • alkoxycarbonyl group having 2 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include methoxycarbonyl, ethoxycarbonyl and n.
  • -Propoxycarbonyl isopropoxycarbonyl, n-butoxycarbonyl, isobutoxycarbonyl, sec-butoxycarbonyl, tert-butoxycarbonyl, 1-pentyloxycarbonyl, 2-pentyloxycarbonyl, 3-pentyloxycarbonyl, isopentyloxycarbonyl, Examples thereof include neopentyloxycarbonyl, tert-pentyloxycarbonyl, 1-hexyloxycarbonyl, 2-hexyloxycarbonyl, 3-hexyloxycarbonyl, cyclohexyloxycarbonyl and the like.
  • Examples of the aryloxycarbonyl group having 7 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include phenoxycarbonyl and p-methyl. Examples thereof include phenoxycarbonyl, naphthyloxycarbonyl, biphenylyloxycarbonyl, anthryloxycarbonyl, phenanthryloxycarbonyl and the like.
  • alkylcarbonylamino group having 2 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include methylcarbonylamino and ethylcarbonyl.
  • Examples of the arylcarbonylamino group having 7 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include phenylcarbonylamino and naphthylcarbonyl.
  • the heterocyclic groups having 2 to 20 carbon atoms which may have a substituent include pyridyl, pyrimidyl, furyl and thienyl. , Tetrahydrofuryl, dioxolanyl, benzoxazole-2-yl, tetrahydropyranyl, pyrrolidyl, imidazolidyl, pyrazolysyl, thiazolidyl, isothiazolydyl, oxazolidyl, isooxazolydyl, piperidyl, piperazyl, morpholinyl and the like. Be done.
  • At least one of Ar 1 , Ar 2 and Ar 3 has a substituent containing a carbonyl group. Is preferable. In this case, it is possible to impart even better transparency to the molded product.
  • substituents containing a carbonyl group include a carboxy group, an aminocarbonyl group, an alkylcarbonyl group having 2 to 20 carbon atoms, an arylcarbonyl group having 7 to 20 carbon atoms, and an alkylcarbonyl group having 2 to 20 carbon atoms.
  • substituents containing a carbonyl group a carboxy group, an aminocarbonyl group, an alkylaminocarbonyl group having 2 to 20 carbon atoms, and an aryl having 7 to 20 carbon atoms from the viewpoint of imparting more excellent transparency to the molded product.
  • An aminocarbonyl group, a dialkylaminocarbonyl group having 3 to 20 carbon atoms, a diarylaminocarbonyl group having 13 to 20 carbon atoms, and an alkylarylaminocarbonyl group having 8 to 20 carbon atoms are preferable, and a carboxy group and an aminocarbonyl group are used. More preferably, an aminocarbonyl group is particularly preferable.
  • the triazine compound represented by the general formula (1) contained in the clearing agent of the present embodiment includes Ar 1 , Ar 2 and Ar 3 . Of these, it is preferable that only one of them has a substituent containing a carbonyl group. Further, in the triazine compound represented by the general formula (1) (A) contained in the clearing agent of the present embodiment , any one of Ar 1 , Ar 2 and Ar 3 is a substituent containing a carbonyl group. It is more preferable that the remaining two have a substituent containing no carbonyl group.
  • an alkyl group having 1 to 20 carbon atoms or a substituent which may have a substituent may be used from the viewpoint of imparting more excellent transparency to the molded product. It is preferably an aryl group having 6 to 20 carbon atoms, more preferably an alkyl group having 1 to 8 carbon atoms or an aryl group having 6 to 12 carbon atoms, and a methyl group, an ethyl group or an n-propyl group.
  • a phenyl group which may have a cyclohexyl group or a substituent is further preferable, and an n-propyl group, a phenyl group or a cyclohexyl group is even more preferable.
  • triazine compound represented by (A) general formula (1) contained in the clearing agent of the present embodiment include, for example, the following compound No. 1 to No. 61 is mentioned. Among these, from the viewpoint of imparting excellent transparency to the molded product, Compound No. 6. Compound No. 39, Compound No. 49, Compound No. 50, Compound No. 58, Compound No. 59, Compound No. 60, Compound No. The triazine compound of 61 is preferable, and the compound No. 6. Compound No. 49, Compound No. 59, Compound No. 60, Compound No. 61 triazine compounds are more preferred.
  • cyanuric chloride is used as a raw material in an organic solvent, and 1 equivalent of each of the phenol compounds corresponding to Ar 1 , Ar 2 and Ar 3 is used. Examples thereof include a method of sequentially reacting in the presence of an equivalent amount of base (triethylamine, sodium hydroxide, etc.).
  • Examples of the alkyl group having 1 to 4 carbon atoms in the general formula (2) include a methyl group, an ethyl group, a propyl group, an n-butyl group, an isobutyl group, a sec-butyl group and a tert-butyl group.
  • Examples of the alkoxy group having 1 to 4 carbon atoms include a methoxy group, an ethoxy group, a propoxy group, an n-butyloxy group, an isobutyloxy group, a sec-butyloxy group and a tert-butyloxy group.
  • Examples of the alkylene group having 3 to 6 carbon atoms in the general formula (2) include a propylene group, a butylene group, a pentylene group, and a hexylene group.
  • Examples of the alkylenedioxy group having 1 to 4 carbon atoms include a methylenedioxy group, an ethylenedioxy group, a propylenedioxy group, and a butylenedioxy group.
  • halogen atom in the general formula (2) examples include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom.
  • R 1 , R 2 , R 3 , R 4 and R 5 are independently hydrogen atoms or carbon atoms, respectively. It is preferably an alkyl group having the number 1 to 4, and X is a ⁇ CH (OH) ⁇ group.
  • acetal compound represented by the general formula (2) contained in the clearing agent of the present embodiment include the following compound No. 62-No. 65 and the like can be mentioned. Among these, from the viewpoint of imparting more excellent transparency to the molded product, Compound No. 62, Compound No. 63 and compound No. The acetal compound represented by 64 is preferable.
  • Examples of the method for producing the acetal compound represented by the general formula (2) include a method of dehydrating and condensing an alditor compound such as sorbitol and arylaldehyde in the presence of an acid catalyst.
  • acetal compounds represented by the general formula (2) (B) contained in the clearing agent of the present embodiment include, for example, Gelol D (trade name) manufactured by Shin Nihon Rika Co., Ltd. Gelol MD (trade name), Gelol DXR (trade name), Gelol E-200 (trade name), Gelol MD-LM30G (trade name), RiKAFAST P1 (trade name), Mirad 3988 manufactured by Milliken & Company (trade name) (Product name), Mirad 3988i (trade name), Mirad NX-8000 (trade name), Mirad NX-8000J (trade name), and the like.
  • the ratio (A) / (B) of the content (parts by mass) of the (A) triazine compound to the content (parts by mass) of the (B) acetal compound is 1/99 to 99/1. ..
  • the values of (A) / (B) are preferably 10/90 or more, and more preferably 25/75 or more.
  • the value of (A) / (B) is preferably 90/10 or less, and more preferably 75/25 or less.
  • the clearing agent of the present embodiment is a compound other than (A) triazine compound and (B) acetal compound, as well as (A) triazine compound and (B) acetal compound, and makes the polyolefin resin transparent. Those having a function to be given may be included.
  • Examples of such compounds include sodium-2,2'-methylenebis (4,6-di-tert-butylphenyl) phosphate, sodium benzoate, 4-tert-butyl benzoate aluminum salt, sodium adipate, 2 Carboxylic acid metal salts such as sodium bicyclo [2.2.1] heptane-2,3-dicarboxylate, calciumcyclohexane-1,2-dicarboxylate, N, N', N "-tris [2-methylcyclohexyl” ] -1,2,3-Propanetricarboxyamide, N, N', N "-tricyclohexyl-1,3,5-benzenetricarboxyamide, N, N'-dicyclohexylnaphthalenedicarboxyamide, 1,3 Examples thereof include amide compounds such as 5-tri (dimethylisopropoilamino) benzene.
  • the content of this compound is (A).
  • the total content of the triazine compound and the content of the (B) acetal compound is preferably 25 parts by mass or less, more preferably 10 parts by mass or less, and 1 part by mass or less. Is even more preferable.
  • the content of this compound may be 0.1 part by mass or more with respect to 100 parts by mass in total of (A) the content of the triazine compound and (B) the content of the acetal compound.
  • the clearing agent of the present embodiment further includes a phenol-based antioxidant, a phosphorus-based antioxidant, a sulfur-based antioxidant, other antioxidants, a hindered amine compound, an ultraviolet absorber, a flame retardant, and a flame retardant aid.
  • Various additives such as lubricants, fillers, hydrotalcites, fatty acid metal salts, antistatic agents, fluorescent whitening agents, pigments and dyes may be contained.
  • phenolic antioxidant examples include 2,6-di-tert-butyl-4-ethylphenol, 2-tert-butyl-4,6-dimethylphenol, styrene phenol, and 2,2′-methylenebis (4).
  • phosphorus-based antioxidants include triphenylphosphite, diisooctylphosphite, heptaxis (dipropylene glycol) triphosphite, triisodecylphosphite, diphenylisooctylphosphite, diisooctylphenylphosphite, and diphenyl.
  • Tridecylphosphite triisooctylphosphite, trilaurylphosphite, diphenylphosphite, tris (dipropylene glycol) phosphite, dioleylhydrogenphosphite, trilauryltrithiophosphite, bis (tridecyl) phosphite, tris (Isodecyl) phosphite, tris (tridecyl) phosphite, diphenyldecylphosphite, dinonylphenylbis (nonylphenyl) phosphite, poly (dipropylene glycol) phenylphosphite, tetraphenyldipropylene glycol diphosphite, trisnonyl Phenyl Phenyl Phenyl Phenyl, Tris (2,4-di-tert-Butylpheny
  • sulfur-based antioxidant examples include tetrakis [methylene-3- (laurylthio) propionate] methane and bis (methyl-4- [3-n-alkyl (C12 / C14) thiopropionyloxy] 5-tert-butylphenyl.
  • antioxidants include N-benzyl- ⁇ -phenylnitrone, N-ethyl- ⁇ -methylnitrone, N-octyl- ⁇ -heptylnitrone, N-lauryl- ⁇ -undecylnitrone, N-tetradecyl- ⁇ .
  • hindered amine compound examples include 2,2,6,6-tetramethyl-4-piperidyl stearate, 1,2,2,6,6-pentamethyl-4-piperidyl stearate, 2,2,6,6- Tetramethyl-4-piperidylbenzoate, bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate, tetrakis (2,2,6,6-tetramethyl-4-piperidyl) -1,2,3 , 4-Butan Tetracarboxylate, Tetrakiss (1,2,2,6,6-Pentamethyl-4-piperidyl) -1,2,3,4-Butane Tetracarboxylate, Bis (2,2,6,6- Tetramethyl-4-piperidyl) di (tridecyl) -1,2,3,4-butanetetracarboxylate, bis (1,2,2,6,6-pentamethyl-4-piperidyl) -di (tridecyl)- 1,2,3,4-butanetetracar
  • Examples of the ultraviolet absorber include 2-hydroxybenzophenones such as 2,4-dihydroxybenzophenone and 5,5'-methylenebis (2-hydroxy-4-methoxybenzophenone); 2- (2-hydroxy-5-methylphenyl).
  • Bentriazole 2- (2-hydroxy-5-tert-octylphenyl) benzotriazole, 2- (2-hydroxy-3,5-di-tert-butylphenyl) -5-chlorobenzotriazole, 2- (2) -Hydroxy-3-tert-butyl-5-methylphenyl) -5-chlorobenzotriazole, 2- (2-hydroxy-3,5-dicumylphenyl) benzotriazole, 2,2'-methylenebis (4-tert- Octyl-6-benzotriazolylphenol), 2- (2-hydroxy-3-tert-butyl-5-carboxyphenyl) benzotriazole polyethylene glycol ester, 2- [2-hydroxy-3- (2-acryloyloxy) Ethy
  • Examples of the flame retardant include triphenyl phosphate, tricresyl phosphate, trixylenyl phosphate, cresyldiphenyl phosphate, cresyl-2,6-dixylenyl phosphate, resorcinolbis (diphenyl phosphate), (1-methylethylidene).
  • Bisphenol A type epoxy resin brominated phenol novolac type epoxy resin, hexabromobenzene, pentabromotoluene, ethylenebis (pentabromophenyl), ethylenebistetrabromophthalimide, 1,2-dibromo-4- (1,2-dibromo) Ethyl) cyclohexane, tetrabromocyclooctane, hexabromocyclododecane, bis (tribromophenoxy) ethane, brominated polyphenylene ether, brominated polystyrene and 2,4,6-tris (tribromophenoxy) -1,3,5- Examples thereof include triazine, tribromophenylmaleimide, tribromophenyl acrylate, tribromophenyl methacrylate, tetrabromobisphenol A type dimethacrylate, pentabromobenzyl acrylate, and bromine-based
  • the lubricant examples include unsaturated fatty acid amides such as oleic acid amide and erucic acid amide; saturated fatty acid amides such as bechenic acid amide and stearic acid amide, butyl stearate, stearyl alcohol, stearic acid monoglyceride, and sorbitan monopalmitite. Examples thereof include sorbitan monostearate, mannitol, stearic acid, hardened castor oil, stearic acid amide, oleic acid amide, and ethylene bisstearic acid amide.
  • unsaturated fatty acid amides such as oleic acid amide and erucic acid amide
  • saturated fatty acid amides such as bechenic acid amide and stearic acid amide, butyl stearate, stearyl alcohol, stearic acid monoglyceride, and sorbitan monopalmitite. Examples thereof include sorbitan monostearate,
  • fillers for example, talc, mica, calcium carbonate, calcium oxide, calcium hydroxide, magnesium carbonate, magnesium hydroxide, magnesium oxide, magnesium sulfate, aluminum hydroxide, barium sulfate, glass powder, glass fiber, clay, dolomite, etc.
  • examples thereof include silica, alumina, potassium titanate whiskers, wallastenite, and fibrous magnesium oxysulfate, and the particle size (fiber diameter, fiber length, and aspect ratio in the fibrous form) can be appropriately selected and used.
  • talc is particularly preferably used because it has an excellent effect of imparting rigidity and is easily available.
  • a surface-treated filler can be used if necessary.
  • Examples of the fatty acid metal salt include a metal salt of a fatty acid having 12 to 20 carbon atoms including a linear or branched fatty acid residue.
  • Examples of the metal ion constituting the fatty acid metal salt include sodium ion, potassium ion, lithium ion, dihydroxyaluminum ion, calcium ion, zinc ion, barium ion, magnesium ion, hydroxyaluminum ion and the like, and among these, sodium ion. , Potassium ion, lithium ion are particularly preferable.
  • Hydrotalcites are complex salt compounds consisting of magnesium, aluminum, hydroxyl groups, carbonic acid groups and arbitrary crystalline water known as natural products and synthetic products, and magnesium or aluminum is partly made of other metals such as alkali metals and zinc. Examples thereof include those substituted with, and those substituted with a hydroxyl group and a carbonic acid group with another anionic group. Hydrotalcites may be obtained by dehydrating crystalline water, and are higher fatty acids such as stearic acid, higher fatty acid metal salts such as oleic acid alkali metal salt, and organic sulfonic acid metals such as dodecylbenzene sulfonic acid alkali metal salt.
  • hydrotalcites may be natural products or synthetic products. Examples of the method for synthesizing hydrotalcites include Japanese Patent Publication No. 46-2280, Japanese Patent Publication No. 50-30039, Japanese Patent Publication No. 51-29129, Japanese Square Root Extraction 3-36839, and Japanese Patent Application Laid-Open No. 61-174270. , Known methods described in JP-A-5-179502, etc. can be mentioned. Further, hydrotalcites can be used without being limited by their crystal structure, crystal particles and the like.
  • antistatic agent examples include a low molecular weight antistatic agent using a nonionic, anionic, cationic or amphoteric surfactant, and a polymer type antistatic agent using a polymer compound.
  • Nonionic surfactants include polyethylene glycol-type nonionic surfactants such as higher alcohol ethylene oxide adducts, fatty acid ethylene oxide adducts, higher alkylamine ethylene oxide adducts, and polyolefin glycol ethylene oxide adducts; fatty acid esters of polyethylene oxide and glycerin.
  • a carboxylate such as an alkali metal salt of a higher fatty acid
  • a sulfate ester salt such as a higher alcohol sulfate ester salt, a higher alkyl ether sulfate ester salt, an alkylbenzene sulfonate, an alkyl sulfonate, a paraffin sulfonate and the like.
  • Phosphoric acid ester salts such as higher alcohol phosphoric acid ester salts and the like can be mentioned
  • examples of the cationic surfactant include quaternary ammonium salts such as alkyltrimethylammonium salt and the like.
  • examples of the amphoteric tenside include amino acid amphoteric tenside agents such as higher alkylaminopropionate, betaine amphoteric tenside agents such as higher alkyldimethylbetaine and higher alkyldihydroxyethyl betaine, and the like.
  • anionic surfactants are preferable, and sulfonates such as alkylbenzene sulfonates, alkyl sulfonates, and paraffin sulfonates are particularly preferable.
  • Examples of the polymer type antistatic agent include ionomer and block polymer having polyethylene glycol as a hydrophilic part.
  • Examples of the ionomer include the ionomer described in JP-A-2010-132927.
  • Examples of the polymer having polyethylene glycol as a hydrophilic portion include a polyether ester amide described in JP-A-7-10989, a polymer composed of polyolefin and polyethylene glycol described in US Pat. No. 6,552,131, and JP-A-2016-023254. Examples thereof include the above-mentioned polymers composed of polyester and polyethylene glycol.
  • Fluorescent whitening agent is a compound that absorbs ultraviolet rays of sunlight or artificial light, converts it into visible light of purple to blue and radiates it, and promotes the whiteness and bluish tint of the molded product.
  • fluorescent whitening agent include benzoxazole compounds C.I. I. Fluorescent Fluorescent 184; Coumarin-based compound C.I. I. Fluorescent Fluorescent 52; diaminostilbene disulphonic acid-based compound C.I. I. Fluorescent Fluorescenter 24, 85, 71 and the like can be mentioned.
  • the pigment is not particularly limited, and a commercially available pigment can also be used.
  • pigments include, for example, Pigment Red 1, 2, 3, 9, 10, 17, 22, 23, 31, 38, 41, 48, 49, 88, 90, 97, 112, 119, 122, 123, 144, 149, 166, 168, 169, 170, 171, 177, 179, 180, 184, 185, 192, 200, 202, 209, 215, 216, 217, 220, 223, 224, 226, 227, 228, 240, 254; Pigment Orange 13, 31, 34, 36, 38, 43, 46, 48, 49, 51, 52, 55, 59, 60, 61, 62, 64, 65, 71; Pigment Yellow 1, 3, 12, 13, 14, 16, 17, 20, 24, 55, 60, 73, 81, 83, 86, 93, 95, 97, 98, 100, 109, 110, 113, 114, 117, 120, 125, 126, 127, 129,
  • dyes examples include azo dyes, anthraquinone dyes, indigoid dyes, triarylmethane dyes, xanthene dyes, alizarin dyes, acrydin dyes, stillben dyes, thiazole dyes, naphthol dyes, quinoline dyes, nitro dyes, indamine dyes, oxazine dyes, and phthalocyanine. Dyes such as dyes and cyanine dyes can be mentioned.
  • the clearing agent of the present embodiment may be a master batch further containing a polyolefin resin.
  • polystyrene-based resins examples include polyethylene-based resins such as low-density polyethylene, linear low-density polyethylene, high-density polyethylene, crosslinked polyethylene, and ultrahigh-molecular-weight polyethylene, homopolypoly, random copolymer polypropylene, and block copolymer.
  • Polypropylene resins such as polypropylene, impact copolymer polypropylene, high impact copolymer polypropylene, maleic anhydride-modified polypropylene, polybutene-1, cycloolefin polymer, poly-3-methyl-1-butene, poly-3-methyl-1-pentene, Examples thereof include ⁇ -olefin polymers such as poly-4-methyl-1-pentene, ethylene-methylmethacrylate copolymers, and ⁇ -olefin copolymers such as ethylene-vinyl acetate copolymers.
  • One of these polyolefin resins may be used alone, or two or more thereof may be used in combination. Further, the polyolefin resin may be alloyed.
  • the type for example, Cheegler catalyst, metallocene catalyst, etc.
  • the type is not particularly limited and is appropriately selected.
  • a polypropylene resin is particularly preferable.
  • the content of the polyolefin resin in the master batch may be, for example, 90% by mass or less, preferably 80% by mass or less, and 60% by mass. The following is more preferable.
  • the content of the polyolefin resin in the masterbatch may be, for example, 20% by mass or more.
  • the clearing agent of the present embodiment may be a one-pack composite additive further blended with a granulating aid such as a binder, wax, solvent, and silica, and granulated.
  • a granulating aid such as a binder, wax, solvent, and silica
  • the resin composition of the present embodiment contains a polyolefin-based resin, a triazine compound represented by the above (A) general formula (1), and an acetal compound represented by the above (B) general formula (2).
  • the ratio (A) / (B) of the content (parts by mass) of the (A) triazine compound to the content (parts by mass) of the (B) acetal compound is 1/99 to 99/1, and is polyolefin-based.
  • the total content of the (A) triazine compound and the (B) acetal compound with respect to 100 parts by mass of the resin is 0.001 to 10 parts by mass.
  • a molded product having excellent transparency can be obtained.
  • Examples of the polyolefin-based resin contained in the resin composition of the present embodiment include the same polyolefin-based resins contained in the above-mentioned masterbatch.
  • the polyolefin-based resin contained in the resin composition is preferably a polypropylene-based resin. In this case, a molded product having excellent heat resistance can be obtained.
  • the ratio (A) / (B) of the content (parts by mass) of the (A) triazine compound to the content (parts by mass) of the (B) acetal compound is It is 1/99 to 99/1.
  • the value of (A) / (B) is preferably 10/90 or more, and more preferably 25/75 or more.
  • the value of (A) / (B) is preferably 90/10 or less, and more preferably 75/25 or less.
  • the total content of the (A) triazine compound and the (B) acetal compound is 0.001 to 10 parts by mass with respect to 100 parts by mass of the polyolefin resin.
  • the total content of the (A) triazine compound and the (B) acetal compound is less than 0.001 part by mass, the transparency of the molded product is not sufficiently excellent.
  • the total content of the (A) triazine compound and the (B) acetal compound exceeds 10 parts by mass, the transparency of the molded product is not sufficiently excellent, and bloom is generated on the surface of the molded product.
  • the (A) triazine compound or (B) acetal compound may be transferred from the molded product to another article.
  • the total content of the (A) triazine compound and (B) acetal compound with respect to 100 parts by mass of the polyolefin resin is preferably 0.01 part by mass or more. It is more preferably 0.02 parts by mass or more, and further preferably 0.05 parts by mass or more. Further, from the viewpoint of further improving the transparency of the molded product and sufficiently suppressing the generation of bloom and the transfer of (A) triazine compound and (B) acetal compound, (A) with respect to 100 parts by mass of the polyolefin-based resin.
  • the total content of the triazine compound and the (B) acetal compound is preferably 2 parts by mass or less, more preferably 1 part by mass or less, further preferably 0.5 parts by mass or less, and 0.3. It is even more preferably parts by mass or less, and particularly preferably 0.1 parts by mass or less.
  • the content of the (A) triazine compound with respect to 100 parts by mass of the polyolefin resin may be, for example, 0.0005 to 9.9995 parts by mass, preferably 0.01 to 5 parts by mass, and 0.01 to 2 parts by mass. It is more preferably parts by mass, more preferably 0.02 to 1 part by mass, further preferably 0.05 to 0.5 parts by mass, and 0.05 to 0.3 parts by mass. It is particularly preferable to have.
  • the content of the (B) acetal compound with respect to 100 parts by mass of the polyolefin resin may be, for example, 0.0005 to 9.9995 parts by mass, preferably 0.01 to 5 parts by mass, and 0.01. It is more preferably to 2 parts by mass, further preferably 0.02 to 1 part by mass, further preferably 0.05 to 0.5 parts by mass, and 0.05 to 0.3 parts by mass. It is particularly preferable that it is a part.
  • the resin composition of the present embodiment includes a phenol-based antioxidant, a phosphorus-based antioxidant, a sulfur-based antioxidant, other antioxidants, and a hindered amine compound. , UV absorbers, flame retardants, flame retardants, lubricants, fillers, hydrotalcites, fatty acid metal salts, antioxidants, fluorescent whitening agents, pigments and dyes, etc. good. Examples of these various additives include the same as those exemplified as the additives that may be contained in the above-mentioned clearing agent.
  • a polyolefin resin is mixed with a triazine compound represented by the above (A) general formula (1) and an acetal compound represented by the above (B) general formula (2). , Including the step of blending.
  • the ratio (A) / (B) of the compounding amount (parts by mass) of the (A) triazine compound and the compounding amount (parts by mass) of the (B) acetal compound is 1/99 to 99/1, and is a polyolefin-based compound.
  • the total amount of the (A) triazine compound and the (B) acetal compound to be blended with respect to 100 parts by mass of the resin is 0.001 to 10 parts by mass.
  • the molded product made of the resin composition produced by the method for producing the resin composition of the present embodiment has excellent transparency.
  • the method for blending the (A) triazine compound and the (B) acetal compound with the polyolefin resin is not particularly limited, and for example, the (A) triazine compound, the (B) acetal compound and, if necessary, the polyolefin resin.
  • examples thereof include a method of blending the above-mentioned various additives and then mixing them using a mixing device such as a Henschel mixer, a mill roll, a Banbury mixer, or a super mixer.
  • the (A) triazine compound, (B) acetal compound and the above-mentioned various additives may be blended with the polyolefin-based resin in the form of the above-mentioned clearing agent.
  • the method for producing the resin composition may be a method including a step of further melt-kneading the mixture obtained by the above-mentioned method using a melt-kneading device such as a single-screw extruder or a twin-screw extruder.
  • the temperature of melt-kneading may be, for example, 180 to 280 ° C.
  • the method for producing the resin composition of the present invention is not limited to the above embodiment, and other production methods include, for example, a polyolefin resin and the triazine compound represented by the above general formula (A).
  • a production method including the step of blending the acetal compound represented by the general formula (2) in the resin composition containing (B), the polyolefin resin and the acetal compound represented by the general formula (2) above. Examples thereof include a production method including a step of blending the triazine compound represented by the general formula (1) in the resin composition containing the above (A).
  • the above-mentioned other production method is a molded product composed of a polyolefin resin and a resin composition containing the triazine compound represented by the above (A) general formula (1), or a polyolefin resin and the above (B) general formula ( It can be suitably used when producing a recycled material using a resin composition obtained by crushing a waste material of a molded product made of a resin composition containing an acetal compound represented by 2) as a raw material.
  • the molded product of this embodiment is obtained by molding the above-mentioned resin composition. This molded product has excellent transparency.
  • Molded products include injection molded products, fibers, flat yarns, biaxially stretched films, uniaxially stretched films, non-stretched films, sheets, thermoforming molded products, extrusion blow molded products, injection blow molded products, injection stretch blow molded products, Examples thereof include molded products such as deformed extrusion molded products and rotary molded products.
  • Preferred specific examples of the molded product include containers such as bottles, jars, cups, buckets, boxes, cans and tanks. When the molded product is a container, the feature of having excellent transparency can be effectively utilized.
  • the method for producing the molded product is not particularly limited, and for example, an injection molding method, an extrusion molding method, a blow molding method, a rotary molding, a vacuum molding method, an inflation molding method, a calendar molding method, a slash molding method, etc.
  • Examples include a dip molding method and a thermoforming molding method.
  • Triazine Compound-1 Compound No. 60
  • Triazine Compound-2 Compound No. 49
  • Triazine Compound-3 Compound No. 61
  • Triazine Compound-4 Compound No. 6
  • Triazine Compound-5 Compound No. 59
  • Acetal Compound-1 Compound No. 63
  • Acetal Compound-2 Compound No. 62
  • Triazine compound-1 A solution prepared by dissolving 6.5 g of sodium hydroxide, 20.4 g of 4-phenylphenol, and 2.06 g of 4-hydroxybenzamide in 300 mL of distilled water was prepared. 11.1 g of cyanuric chloride was dissolved in 300 mL of acetone in another flask and cooled to 5 ° C. in an ice bath. The prepared solution was slowly added dropwise, and after the addition, the mixture was stirred at room temperature for 4 hours. The generated precipitate was filtered off, washed with distilled water and dried, and then compound No.
  • Triazine compound-2 was prepared by the same procedure as above except that 4-phenylphenol, 4-cyclohexylphenol, 4-hydroxybenzamide and cyanuric chloride were used as raw materials.
  • Triazine compound-3 was prepared by the same procedure as above except that 4-cyclohexylphenol and cyanuric chloride were used as raw materials.
  • Triazine compound-4 was prepared by the same procedure as above except that p-cresol, 4-hydroxybenzamide and cyanuric chloride were used as raw materials.
  • Triazine compound-5 was prepared by the same procedure as above except that 4-phenylphenol, 4-n-propylphenol, 4-hydroxybenzamide and cyanuric chloride were used as raw materials.
  • FIG. 1 is a cross-sectional view of a laminate produced in the evaluation of transparency
  • FIG. 2 is a diagram for explaining a point of measuring the transmittance in the evaluation of transparency of an example, and the sample is above. It is a figure seen from.
  • 3 mm of a propylene random copolymer load 2.16 kg, melt flow rate 12 g / 10 min at a measurement temperature of 230 ° C., product name "Prime Polypro R720" manufactured by Prime Polymer Co., Ltd.
  • a square film 2 having a size of ⁇ 3 mm ⁇ 300 ⁇ m was placed.
  • the second cover glass 4 was placed on the clearing agent 3 to obtain a laminated body 10.
  • the laminate 10 thus obtained is placed on a hot stage with a temperature control function with the surface formed of the first cover glass 1 facing down, and then a 1 g weight is placed on the upper surface of the second cover glass 4.
  • the laminated body 10 was pressed uniformly.
  • the pressed laminate 10 is heated from room temperature to 220 ° C. at a rate of 100 ° C./min using a heater of a hot stage, held at 220 ° C. for 3 min, and then cooled to room temperature at 100 ° C./min. bottom.
  • the laminate after the heat treatment was used as the sample 20, and the light transmittance when the sample 20 was placed between the two polarizing plates placed on the cloth Nicol was measured to measure Examples 1 to 8 and Comparative Examples 1 to 1.
  • the transparency of the molded product made of the resin composition containing the clearing agent of No. 2 was evaluated. Specifically, using a microultraviolet visible spectrophotometer (MSV-5100 manufactured by JASCO Corporation), the measurement wavelength was set to 500 nm, the IN aperture was set to 30 ⁇ m, and the OUT aperture was set to 100 ⁇ m, and the first polarizing plate (polarized light) was set from the light source. The intensity I of the light passed through the sample 20 and the second polarizing plate and detected by the detector was measured, and the transmittance T (%) was calculated.
  • MSV-5100 microultraviolet visible spectrophotometer
  • the transmittance T (%) was calculated as follows. That is, the intensity of light when the measurement is performed by arranging only the first polarizing plate (polarizer) without arranging the sample and the second polarizing plate (photometer) is set to I 100 , and the sample and the second polarizing plate (photometer) are arranged. Light when the first polarizing plate (polarizer) is placed and the black plate is placed instead of the second polarizing plate (photometer) to perform the measurement without arranging the polarizing plate (photometer) of the above.
  • the smallest value among 28 is used as an index of the transparency of the molded product composed of the resin composition containing the clearing agents of Examples 1 to 8 and Comparative Examples 1 and 2, and "Transmittance (%)) is shown in Tables 1 and 2. It was shown as.
  • the reason why the measured value of the transmittance obtained as described above serves as an index of the transparency of the molded product made of the resin composition containing the transparent agent is as follows. That is, in the above measurement, when the light from the light source polarized by the first polarizing plate (polarizer) is incident on the sample and the incident light is scattered by the coarse crystals of the polyolefin resin in the sample, the scattered light Since the plane of polarization rotates, the scattered light passes through the second polarizing plate (photometer) and is detected by the detector. On the other hand, when the incident light is not scattered in the sample, the incident light is blocked by the detector and is not detected by the detector.
  • the smaller the measured value of the transmittance in the above measurement the smaller the ratio of the scattered light to the total incident light. Therefore, it can be said that the smaller the measured value of the transmittance in the above measurement, the more excellent the transparency of the molded product made of the resin composition containing the transparent agent.
  • the transparent agent of the present invention can impart excellent transparency to the molded product.

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Abstract

The present invention provides: a transparentizing agent which is capable of imparting a molded article with excellent transparency; a resin composition which contains this transparentizing agent; a molded article of this resin composition; and a method for producing a resin composition. This transparentizing agent contains (A) a triazine compound which is represented by general formula (1) (in general formula (1), each of Ar1, Ar2 and Ar3 independently represents an unsubstituted phenyl group or a substituted phenyl group), and (B) an acetal compound which is represented by general formula (2) (in general formula (2), R1 represents a hydrogen atom or an alkyl group having from 1 to 4 carbon atoms; each of R2, R3, R4 and R5 independently represents a hydrogen atom or the like, or alternatively, R2 and R3, or R4 and R5 may combine with each other to form an alkylene group having from 3 to 6 carbon atoms, or the like; and X represents a single bond or the like); and the ratio of the content (parts by mass) of the triazine compound (A) to the content (parts by mass) of the acetal compound (B), namely (A)/(B) is from 1/99 to 99/1.

Description

透明化剤、これを含む樹脂組成物、その成形品および樹脂組成物の製造方法A clearing agent, a resin composition containing the same, a molded product thereof, and a method for producing the resin composition.
 本発明は、透明化剤、これを含む樹脂組成物、その成形品および樹脂組成物の製造方法に関し、より詳しくは、成形品に優れた透明性を付与することができる透明化剤、これを含む樹脂組成物、その成形品および樹脂組成物の製造方法に関する。 The present invention relates to a clearing agent, a resin composition containing the same, a molded product thereof, and a method for producing the resin composition. The present invention relates to a resin composition containing, a molded product thereof, and a method for producing the resin composition.
 ポリプロピレンなどのポリオレフィン系樹脂は成形加工性、耐熱性、力学的特性等に優れ、さらに比重が小さいという特徴を有しており、フィルム、シートおよび各種成形品(構造部品等)に広く利用されている。しかしながら、成形品の用途によっては、ポリオレフィン系樹脂からなる成形品は、十分に優れた透明性を有するものとは言えない場合があった。 Polyolefin-based resins such as polypropylene are excellent in molding processability, heat resistance, mechanical properties, etc., and have a small specific gravity, and are widely used for films, sheets, and various molded products (structural parts, etc.). There is. However, depending on the use of the molded product, the molded product made of a polyolefin resin may not be said to have sufficiently excellent transparency.
 ポリオレフィン系樹脂からなる成形品の透明性を改善する方法としては、ポリオレフィン系樹脂に透明化剤を添加する方法が知られている。ポリオレフィン系樹脂に添加する透明化剤として、例えば、特許文献1では、芳香族リン酸エステル金属塩およびアセタール化合物を含む透明化剤が提案されている。 As a method for improving the transparency of a molded product made of a polyolefin resin, a method of adding a clearing agent to the polyolefin resin is known. As a clearing agent to be added to a polyolefin resin, for example, Patent Document 1 proposes a clearing agent containing an aromatic phosphoric acid ester metal salt and an acetal compound.
特開2017-036356号公報Japanese Unexamined Patent Publication No. 2017-036356
 しかしながら、特許文献1記載の透明化剤は、成形品に優れた透明性を付与する観点において、さらなる改善の余地があった。 However, the clearing agent described in Patent Document 1 has room for further improvement from the viewpoint of imparting excellent transparency to the molded product.
 そこで、本発明の目的は、成形品に優れた透明性を付与することができる透明化剤、これを含む樹脂組成物、その成形品および樹脂組成物の製造方法を提供することにある。 Therefore, an object of the present invention is to provide a clearing agent capable of imparting excellent transparency to a molded product, a resin composition containing the transparent agent, a molded product thereof, and a method for producing the resin composition.
 本発明者らは、上記課題を解決すべく鋭意検討を重ねた結果、特定の構造を有するトリアジン化合物および特定の構造を有するアセタール化合物を含む透明化剤を併用することにより、上記課題を解消することができることを見出し、本発明を完成するに至った。 As a result of diligent studies to solve the above problems, the present inventors solve the above problems by using a clearing agent containing a triazine compound having a specific structure and an acetal compound having a specific structure in combination. We have found that we can do this, and have completed the present invention.
 すなわち、本発明の透明化剤は、(A)下記一般式(1)、
Figure JPOXMLDOC01-appb-I000011
(一般式(1)中、Ar、ArおよびArは、それぞれ独立に、無置換のフェニル基または置換基を有するフェニル基を表す。)で表されるトリアジン化合物と、(B)下記一般式(2)、
Figure JPOXMLDOC01-appb-I000012
(一般式(2)中、Rは水素原子または炭素原子数1~4のアルキル基を表す。R、R、RおよびRはそれぞれ独立に水素原子、ハロゲン原子、シアノ基、炭素原子数1~4のアルキル基または炭素原子数1~4のアルコキシ基を表し、あるいはRおよびRまたはRおよびRが互いに連結して炭素原子数3~6のアルキレン基または炭素原子数1~4のアルキレンジオキシ基を表す。Xは単結合、-CH(OH)-基または-CH(OH)CH(OH)-基を表す。)で表されるアセタール化合物と、を含み、前記(A)トリアジン化合物の含有量(質量部)と前記(B)アセタール化合物の含有量(質量部)との比(A)/(B)が1/99~99/1であることを特徴とするものである。
That is, the clearing agent of the present invention has (A) the following general formula (1),
Figure JPOXMLDOC01-appb-I000011
(In the general formula (1), Ar 1 , Ar 2 and Ar 3 each independently represent an unsubstituted phenyl group or a phenyl group having a substituent), and (B) the following General formula (2),
Figure JPOXMLDOC01-appb-I000012
(In the general formula (2), R 1 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. R 2 , R 3 , R 4 and R 5 are independent hydrogen atoms, halogen atoms and cyano groups, respectively. Represents an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, or an alkylene group or carbon having 3 to 6 carbon atoms in which R 2 and R 3 or R 4 and R 5 are linked to each other. Represents an alkylenedioxy group having 1 to 4 atoms. X represents a single bond, an acetal compound represented by -CH (OH) -group or -CH (OH) CH (OH) -group. The ratio (A) / (B) of the content (parts by mass) of the (A) triazine compound to the content (parts by mass) of the (B) acetal compound is 1/99 to 99/1. It is characterized by.
 本発明の透明化剤においては、前記一般式(1)のAr、ArおよびArのうち少なくとも1つが、カルボニル基を含む置換基を有することが好ましい。また、本発明の透明化剤においては、前記一般式(2)中のR、R、R、RおよびRがそれぞれ独立に水素原子または炭素原子数1~4のアルキル基であり、Xが-CH(OH)-基であることが好ましい。 In the clearing agent of the present invention, it is preferable that at least one of Ar 1 , Ar 2 and Ar 3 of the general formula (1) has a substituent containing a carbonyl group. Further, in the clearing agent of the present invention, R 1 , R 2 , R 3 , R 4 and R 5 in the general formula (2) are independently hydrogen atoms or alkyl groups having 1 to 4 carbon atoms, respectively. Yes, and it is preferable that X is a -CH (OH) -group.
 本発明の樹脂組成物は、ポリオレフィン系樹脂と、(A)下記一般式(1)、
Figure JPOXMLDOC01-appb-I000013
(一般式(1)中、Ar、ArおよびArは、それぞれ独立に、無置換のフェニル基または置換基を有するフェニル基を表す。)で表されるトリアジン化合物と、(B)下記一般式(2)、
Figure JPOXMLDOC01-appb-I000014
(一般式(2)中、Rは水素原子または炭素原子数1~4のアルキル基を表す。R、R、RおよびRはそれぞれ独立に水素原子、ハロゲン原子、シアノ基、炭素原子数1~4のアルキル基または炭素原子数1~4のアルコキシ基を表し、あるいはRおよびRまたはRおよびRが互いに連結して炭素原子数3~6のアルキレン基または炭素原子数1~4のアルキレンジオキシ基を表す。Xは単結合、-CH(OH)-基または-CH(OH)CH(OH)-基を表す。)で表されるアセタール化合物と、を含み、前記(A)トリアジン化合物の含有量(質量部)と前記(B)アセタール化合物の含有量(質量部)との比(A)/(B)が1/99~99/1であり、前記ポリオレフィン系樹脂100質量部に対する前記(A)トリアジン化合物および前記(B)アセタール化合物の合計含有量が0.001~10質量部であることを特徴とするものである。
The resin composition of the present invention comprises a polyolefin resin and (A) the following general formula (1),
Figure JPOXMLDOC01-appb-I000013
(In the general formula (1), Ar 1 , Ar 2 and Ar 3 each independently represent an unsubstituted phenyl group or a phenyl group having a substituent), and (B) the following General formula (2),
Figure JPOXMLDOC01-appb-I000014
(In the general formula (2), R 1 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. R 2 , R 3 , R 4 and R 5 are independent hydrogen atoms, halogen atoms and cyano groups, respectively. Represents an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, or an alkylene group or carbon having 3 to 6 carbon atoms in which R 2 and R 3 or R 4 and R 5 are linked to each other. Represents an alkylenedioxy group having 1 to 4 atoms. X represents a single bond, an acetal compound represented by -CH (OH) -group or -CH (OH) CH (OH) -group. The ratio (A) / (B) of the content (parts by mass) of the (A) triazine compound to the content (parts by mass) of the (B) acetal compound is 1/99 to 99/1. The total content of the (A) triazine compound and the (B) acetal compound with respect to 100 parts by mass of the polyolefin-based resin is 0.001 to 10 parts by mass.
 本発明の樹脂組成物においては、前記ポリオレフィン系樹脂が、ポリプロピレン系樹脂であることが好ましい。 In the resin composition of the present invention, the polyolefin-based resin is preferably a polypropylene-based resin.
 本発明の成形品は、本発明の樹脂組成物を成形して得られることを特徴とするものである。 The molded product of the present invention is characterized by being obtained by molding the resin composition of the present invention.
 本発明の成形品としては容器が好ましい。 A container is preferable as the molded product of the present invention.
 本発明の樹脂組成物の製造方法は、ポリオレフィン系樹脂に、(A)下記一般式(1)、
Figure JPOXMLDOC01-appb-I000015
(一般式(1)中、Ar、ArおよびArは、それぞれ独立に、無置換のフェニル基または置換基を有するフェニル基を表す。)で表されるトリアジン化合物と、(B)下記一般式(2)、
Figure JPOXMLDOC01-appb-I000016
(一般式(2)中、Rは水素原子または炭素原子数1~4のアルキル基を表す。R、R、RおよびRはそれぞれ独立に水素原子、ハロゲン原子、シアノ基、炭素原子数1~4のアルキル基または炭素原子数1~4のアルコキシ基を表し、あるいはRおよびRまたはRおよびRが互いに連結して炭素原子数3~6のアルキレン基または炭素原子数1~4のアルキレンジオキシ基を表す。Xは単結合、-CH(OH)-基または-CH(OH)CH(OH)-基を表す。)で表されるアセタール化合物と、を配合する工程を含み、前記(A)トリアジン化合物の配合量(質量部)と前記(B)アセタール化合物の配合量(質量部)との比(A)/(B)が1/99~99/1であり、前記ポリオレフィン系樹脂100質量部に対する前記(A)トリアジン化合物および前記(B)アセタール化合物の合計配合量が0.001~10質量部であることを特徴とするものである。
The method for producing the resin composition of the present invention is to use a polyolefin resin according to (A) the following general formula (1).
Figure JPOXMLDOC01-appb-I000015
(In the general formula (1), Ar 1 , Ar 2 and Ar 3 each independently represent an unsubstituted phenyl group or a phenyl group having a substituent), and (B) the following General formula (2),
Figure JPOXMLDOC01-appb-I000016
(In the general formula (2), R 1 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. R 2 , R 3 , R 4 and R 5 are independent hydrogen atoms, halogen atoms and cyano groups, respectively. Represents an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, or an alkylene group or carbon having 3 to 6 carbon atoms in which R 2 and R 3 or R 4 and R 5 are linked to each other. Represents an alkylenedioxy group having 1 to 4 atoms. X represents a single bond, an acetal compound represented by -CH (OH) -group or -CH (OH) CH (OH) -group. Including the step of blending, the ratio (A) / (B) of the blending amount (parts by mass) of the (A) triazine compound to the blending amount (parts by mass) of the (B) acetal compound is 1/99 to 99 /. The total amount of the (A) triazine compound and the (B) acetal compound is 0.001 to 10 parts by mass with respect to 100 parts by mass of the polyolefin resin.
 本発明の樹脂組成物の製造方法の一好適な実施の形態は、ポリオレフィン系樹脂と(A)下記一般式(1)、
Figure JPOXMLDOC01-appb-I000017
(一般式(1)中、Ar、ArおよびArは、それぞれ独立に、無置換のフェニル基または置換基を有するフェニル基を表す。)で表されるトリアジン化合物とを含む樹脂組成物に(B)下記一般式(2)、
Figure JPOXMLDOC01-appb-I000018
(一般式(2)中、Rは水素原子または炭素原子数1~4のアルキル基を表す。R、R、RおよびRはそれぞれ独立に水素原子、ハロゲン原子、シアノ基、炭素原子数1~4のアルキル基または炭素原子数1~4のアルコキシ基を表し、あるいはRおよびRまたはRおよびRが互いに連結して炭素原子数3~6のアルキレン基または炭素原子数1~4のアルキレンジオキシ基を表す。Xは単結合、-CH(OH)-基または-CH(OH)CH(OH)-基を表す。)で表されるアセタール化合物を配合する工程を含み、前記(A)トリアジン化合物の配合量(質量部)と前記(B)アセタール化合物の配合量(質量部)との比(A)/(B)が1/99~99/1であり、前記ポリオレフィン系樹脂100質量部に対する前記(A)トリアジン化合物および前記(B)アセタール化合物の合計配合量が0.001~10質量部であることを特徴とする。
One preferred embodiment of the method for producing a resin composition of the present invention is a polyolefin resin and (A) the following general formula (1).
Figure JPOXMLDOC01-appb-I000017
(In the general formula (1), Ar 1 , Ar 2 and Ar 3 each independently represent an unsubstituted phenyl group or a phenyl group having a substituent.) A resin composition containing a triazine compound represented by the above. (B) The following general formula (2),
Figure JPOXMLDOC01-appb-I000018
(In the general formula (2), R 1 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. R 2 , R 3 , R 4 and R 5 are independent hydrogen atoms, halogen atoms and cyano groups, respectively. Represents an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, or an alkylene group or carbon having 3 to 6 carbon atoms in which R 2 and R 3 or R 4 and R 5 are linked to each other. It represents an alkylenedioxy group having 1 to 4 atoms. X represents a single bond, -CH (OH) -group or -CH (OH) CH (OH) -group). Including the step, the ratio (A) / (B) of the compounding amount (parts by mass) of the (A) triazine compound to the compounding amount (parts by mass) of the (B) acetal compound is 1/99 to 99/1. The total amount of the (A) triazine compound and the (B) acetal compound is 0.001 to 10 parts by mass with respect to 100 parts by mass of the polyolefin resin.
 本発明の樹脂組成物の製造方法の他の実施の形態は、ポリオレフィン系樹脂と(B)下記一般式(2)、
Figure JPOXMLDOC01-appb-I000019
(一般式(2)中、Rは水素原子または炭素原子数1~4のアルキル基を表す。R、R、RおよびRはそれぞれ独立に水素原子、ハロゲン原子、シアノ基、炭素原子数1~4のアルキル基または炭素原子数1~4のアルコキシ基を表し、あるいはRおよびRまたはRおよびRが互いに連結して炭素原子数3~6のアルキレン基または炭素原子数1~4のアルキレンジオキシ基を表す。Xは単結合、-CH(OH)-基または-CH(OH)CH(OH)-基を表す。)で表されるアセタール化合物とを含む樹脂組成物に、(A)下記一般式(1)、
Figure JPOXMLDOC01-appb-I000020
(一般式(1)中、Ar、ArおよびArは、それぞれ独立に、無置換のフェニル基または置換基を有するフェニル基を表す。)で表されるトリアジン化合物を配合する工程を含み、前記(A)トリアジン化合物の配合量(質量部)と前記(B)アセタール化合物の配合量(質量部)との比(A)/(B)が1/99~99/1であり、前記ポリオレフィン系樹脂100質量部に対する前記(A)トリアジン化合物および前記(B)アセタール化合物の合計配合量が0.001~10質量部であることを特徴とする。
Other embodiments of the method for producing the resin composition of the present invention include polyolefin resins and (B) the following general formula (2).
Figure JPOXMLDOC01-appb-I000019
(In the general formula (2), R 1 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. R 2 , R 3 , R 4 and R 5 are independent hydrogen atoms, halogen atoms and cyano groups, respectively. Represents an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, or an alkylene group or carbon having 3 to 6 carbon atoms in which R 2 and R 3 or R 4 and R 5 are linked to each other. Represents an alkylenedioxy group having 1 to 4 atoms. X represents a single bond, an acetal compound represented by -CH (OH) -group or -CH (OH) CH (OH) -group. In the resin composition, (A) the following general formula (1),
Figure JPOXMLDOC01-appb-I000020
(In the general formula (1), Ar 1 , Ar 2 and Ar 3 each independently represent an unsubstituted phenyl group or a phenyl group having a substituent.) Including a step of blending a triazine compound represented by the above. The ratio (A) / (B) of the compounding amount (parts by mass) of the (A) triazine compound to the compounding amount (parts by mass) of the (B) acetal compound is 1/99 to 99/1. The total amount of the (A) triazine compound and the (B) acetal compound to be blended with respect to 100 parts by mass of the polyolefin resin is 0.001 to 10 parts by mass.
 本発明によれば、成形品に優れた透明性を付与することができる透明化剤、これを含む樹脂組成物、その成形品および樹脂組成物の製造方法を提供することができる。 According to the present invention, it is possible to provide a transparent agent capable of imparting excellent transparency to a molded product, a resin composition containing the transparent agent, a molded product thereof, and a method for producing the resin composition.
実施例の透明性の評価において作製される積層体の断面図である。It is sectional drawing of the laminated body produced in the evaluation of the transparency of an Example. 実施例の透明性の評価において透過率を測定する点を説明するための図である。It is a figure for demonstrating the point of measuring the transmittance in the evaluation of the transparency of an Example.
 以下、本発明の実施形態について詳細に説明する。先ず、本発明の実施形態に係る透明化剤について説明する。 Hereinafter, embodiments of the present invention will be described in detail. First, the clearing agent according to the embodiment of the present invention will be described.
<透明化剤>
 本実施形態の透明化剤は、(A)下記一般式(1)で表されるトリアジン化合物と(B)下記一般式(2)で表されるアセタール化合物とを含む。そして、(A)トリアジン化合物の含有量(質量部)と(B)アセタール化合物の含有量(質量部)との比(A)/(B)が1/99~99/1である。
<Transparent agent>
The clearing agent of the present embodiment includes (A) a triazine compound represented by the following general formula (1) and (B) an acetal compound represented by the following general formula (2). The ratio (A) / (B) of the content (parts by mass) of the (A) triazine compound to the content (parts by mass) of the (B) acetal compound is 1/99 to 99/1.
Figure JPOXMLDOC01-appb-I000021
Figure JPOXMLDOC01-appb-I000021
Figure JPOXMLDOC01-appb-I000022
Figure JPOXMLDOC01-appb-I000022
 ここで、一般式(1)中、Ar、ArおよびArは、それぞれ独立に、無置換のフェニル基または置換基を有するフェニル基を表し、一般式(2)中、Rは水素原子または炭素原子数1~4のアルキル基を表す。R、R、RおよびRはそれぞれ独立に水素原子、ハロゲン原子、シアノ基、炭素原子数1~4のアルキル基または炭素原子数1~4のアルコキシ基を表し、あるいはRおよびRまたはRおよびRが互いに連結して炭素原子数3~6のアルキレン基または炭素原子数1~4のアルキレンジオキシ基を表す。Xは単結合、-CH(OH)-基または-CH(OH)CH(OH)-基を表す。 Here, in the general formula (1), Ar 1 , Ar 2 and Ar 3 each independently represent an unsubstituted phenyl group or a phenyl group having a substituent, and in the general formula (2), R 1 is hydrogen. Represents an atom or an alkyl group having 1 to 4 carbon atoms. R 2 , R 3 , R 4 and R 5 independently represent a hydrogen atom, a halogen atom, a cyano group, an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, or R 2 and R 3 or R 4 and R 5 are linked to each other to represent an alkylene group having 3 to 6 carbon atoms or an alkylene dioxy group having 1 to 4 carbon atoms. X represents a single bond, -CH (OH) -group or -CH (OH) CH (OH) -group.
 本実施形態の透明化剤によれば、成形品に優れた透明性を付与することができる。 According to the transparent agent of the present embodiment, excellent transparency can be imparted to the molded product.
 一般式(1)のAr、ArおよびArが有する置換基としては、例えばハロゲン原子、ヒドロキシ基、カルボキシ基、置換基を有していてもよい炭素原子数1~20のアルキル基、置換基を有していてもよい炭素原子数6~20のアリール基、置換基を有していてもよいアミノ基、置換基を有していてもよいアミノカルボニル基(カルバモイル基ともいう)、ニトロ基、シアノ基、チオール基、スルホ基、スルホンアミド基、ホルミル基、置換基を有していてもよい炭素原子数1~20のアルコキシ基、置換基を有していてもよい炭素原子数6~20のアリールオキシ基、置換基を有していてもよい炭素原子数1~20のアルキルチオ基、置換基を有していてもよい炭素原子数2~20のアルキルカルボニル基、置換基を有していてもよい炭素原子数7~20のアリールカルボニル基、置換基を有していてもよい炭素原子数2~20のアルキルカルボニルオキシ基、置換基を有していてもよい炭素原子数7~20のアリールカルボニルオキシ基、置換基を有していてもよい炭素原子数2~20のアルコキシカルボニル基、置換基を有していてもよい炭素原子数7~20のアリールオキシカルボニル基、置換基を有していてもよいアミノカルボニル基、置換基を有していてもよい炭素原子数2~20のアルキルカルボニルアミノ基、置換基を有していてもよい炭素原子数7~20のアリールカルボニルアミノ基、置換基を有してもよい炭素原子数2~20の複素環基等が挙げられる。ここで、カルボキシ基、スルホ基は塩を形成していてもよい。 Examples of the substituents of Ar 1 , Ar 2 and Ar 3 of the general formula (1) include a halogen atom, a hydroxy group, a carboxy group, and an alkyl group having 1 to 20 carbon atoms which may have a substituent. An aryl group having 6 to 20 carbon atoms which may have a substituent, an amino group which may have a substituent, an aminocarbonyl group which may have a substituent (also referred to as a carbamoyl group), A nitro group, a cyano group, a thiol group, a sulfo group, a sulfonamide group, a formyl group, an alkoxy group having 1 to 20 carbon atoms which may have a substituent, and a number of carbon atoms which may have a substituent. 6 to 20 aryloxy groups, alkylthio groups having 1 to 20 carbon atoms which may have a substituent, alkylcarbonyl groups having 2 to 20 carbon atoms which may have a substituent, and substituents. It may have an arylcarbonyl group having 7 to 20 carbon atoms, an alkylcarbonyloxy group having 2 to 20 carbon atoms which may have a substituent, and a carbon atom which may have a substituent. 7 to 20 arylcarbonyloxy groups, alkoxycarbonyl groups having 2 to 20 carbon atoms which may have a substituent, aryloxycarbonyl groups having 7 to 20 carbon atoms which may have a substituent, An aminocarbonyl group which may have a substituent, an alkylcarbonylamino group which may have a substituent and has 2 to 20 carbon atoms, and an alkylcarbonylamino group which may have a substituent and which has 7 to 20 carbon atoms. Examples thereof include an arylcarbonylamino group and a heterocyclic group having 2 to 20 carbon atoms which may have a substituent. Here, the carboxy group and the sulfo group may form a salt.
 Ar、ArおよびArが有する置換基のうち、置換基を有していてもよい基が有する置換基としては、例えばメチル、エチル、プロピル、イソプロピル、シクロプロピル、ブチル、sec-ブチル、tert-ブチル、イソブチル、アミル、イソアミル、tert-アミル、シクロペンチル、ヘキシル、2-ヘキシル、3-ヘキシル、シクロヘキシル、ビシクロヘキシル、1-メチルシクロヘキシル、ヘプチル、2-ヘプチル、3-ヘプチル、イソヘプチル、tert-ヘプチル、n-オクチル、イソオクチル、tert-オクチル、2-エチルヘキシル、ノニル、イソノニル、デシル等のアルキル基、ビニル、1-メチルエテニル、2-メチルエテニル、2-プロペニル、1-メチル-3-プロペニル、3-ブテニル、1-メチル-3-ブテニル、イソブテニル、3-ペンテニル、4-ヘキセニル、シクロヘキセニル、ビシクロヘキセニル、ヘプテニル、オクテニル、デセニル、ぺンタデセニル、エイコセニル、トリコセニル等のアルケニル基、ベンジル、フェネチル、ジフェニルメチル、トリフェニルメチル、スチリル、シンナミル等のアリールアルキル基、フェニル、ナフチル等のアリール基、ピリジル、ピリミジル、ピリダジル、ピペリジル、ピラニル、ピラゾリル、トリアジル、ピロリル、キノリル、イソキノリル、イミダゾリル、ベンゾイミダゾリル、トリアゾリル、フリル、フラニル、ベンゾフラニル、チエニル、チオフェニル、ベンゾチオフェニル、チアジアゾリル、チアゾリル、ベンゾチアゾリル、オキサゾリル、ベンゾオキサゾリル、イソチアゾリル、イソオキサゾリル、インドリル、2-ピロリジノン-1-イル、2-ピペリドン-1-イル、2,4-ジオキシイミダゾリジン-3-イル、2,4-ジオキシオキサゾリジン-3-イル等の複素環基、フッ素、塩素、臭素、ヨウ素等のハロゲン原子、スルホンアミド基、スルホニル基、カルボキシ基、シアノ基、スルホ基、水酸基、ニトロ基、メルカプト基、イミド基、カルバモイル基、スルホンアミド基等が挙げられる。ここで、カルボキシ基およびスルホ基は、塩を形成していてもよい。 Among the substituents of Ar 1 , Ar 2 and Ar 3 , the substituents of the group which may have a substituent include, for example, methyl, ethyl, propyl, isopropyl, cyclopropyl, butyl, sec-butyl, and the like. tert-butyl, isobutyl, amyl, isoamyl, tert-amyl, cyclopentyl, hexyl, 2-hexyl, 3-hexyl, cyclohexyl, bicyclohexyl, 1-methylcyclohexyl, heptyl, 2-heptyl, 3-heptyl, isoheptyl, tert- Alkyl groups such as heptyl, n-octyl, isooctyl, tert-octyl, 2-ethylhexyl, nonyl, isononyl, decyl, vinyl, 1-methylethenyl, 2-methylethenyl, 2-propenyl, 1-methyl-3-propenyl, 3- Butenyl, 1-methyl-3-butenyl, isobutenyl, 3-pentenyl, 4-hexenyl, cyclohexenyl, bicyclohexenyl, heptenyl, octenyl, decenyl, pentadecenyl, eicosenyl, alkenyl groups such as tricosenyl, benzyl, phenethyl, diphenylmethyl, Arylalkyl groups such as triphenylmethyl, styryl, cinnamyl, aryl groups such as phenyl and naphthyl, pyridyl, pyrimidyl, pyridadyl, piperidyl, pyranyl, pyrazolyl, triadyl, pyrrolyl, quinolyl, isoquinolyl, imidazolyl, benzoimidazolyl, triazolyl, frills, flanyl , Benzofuranyl, thienyl, thiophenyl, benzothiophenyl, thiadiazolyl, thiazolyl, benzothiazolyl, oxazolyl, benzoxazolyl, isothiazolyl, isooxazolyl, indolyl, 2-pyrrolidinone-1-yl, 2-piperidone-1-yl, 2,4- Heterocyclic groups such as dioxyimidazolidine-3-yl and 2,4-dioxyoxazolidine-3-yl, halogen atoms such as fluorine, chlorine, bromine and iodine, sulfonamide groups, sulfonyl groups, carboxy groups and cyano groups. , Sulf group, hydroxyl group, nitro group, mercapto group, imide group, carbamoyl group, sulfonamide group and the like. Here, the carboxy group and the sulfo group may form a salt.
 一般式(1)中のAr、ArおよびArが有する置換基の、ハロゲン原子の例としては、フッ素、塩素、臭素、ヨウ素が挙げられる。 Examples of halogen atoms of the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include fluorine, chlorine, bromine and iodine.
 一般式(1)中のAr、ArおよびArが有する置換基の、置換基を有していてもよい炭素原子数1~20のアルキル基としては、メチル、エチル、n-プロピル、イソプロピル、n-ブチル、イソブチル、sec-ブチル、tert-ブチル、n-ペンチル、イソペンチル、ネオペンチル、tert-アミル、1,2-ジメチルプロピル、n-ヘキシル、シクロヘキシル、1,3-ジメチルブチル、1-イソプロピルプロピル、1,2-ジメチルブチル、n-ヘプチル、2-ヘプチル、1,4-ジメチルペンチル、tert-ヘプチル、2-メチル-1-イソプロピルプロピル、1-エチル-3-メチルブチル、n-オクチル、tert-オクチル、2-エチルヘキシル、2-メチルヘキシル、2-プロピルヘキシル、n-ノニル、イソノニル、n-デシル、イソデシル、n-ウンデシル、イソウンデシル、n-ドデシル、イソドデシル、n-トリデシル、イソトリデシル、n-テトラデシル、イソテトラデシル、n-ペンタデシル、イソペンタデシル、n-ヘキサデシル、イソヘキサデシル、n-ヘプタデシル、イソヘプタデシル、n-オクタデシル、イソオクタデシル、n-ノナデシル、イソノナデシル、n-イコシル、イソイコシル、シクロペンチル、シクロヘキシル、シクロオクチル、シクロドデシル、ベンジル、フェネチル、2-フェニルプロパン-2-イル、スチリル、シンナミル、ジフェニルメチル、トリフェニルメチル等が挙げられる。 Of the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1), the alkyl groups having 1 to 20 carbon atoms which may have a substituent include methyl, ethyl and n-propyl. Isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, tert-amyl, 1,2-dimethylpropyl, n-hexyl, cyclohexyl, 1,3-dimethylbutyl, 1- Isopropylpropyl, 1,2-dimethylbutyl, n-heptyl, 2-heptyl, 1,4-dimethylpentyl, tert-heptyl, 2-methyl-1-isopropylpropyl, 1-ethyl-3-methylbutyl, n-octyl, tert-octyl, 2-ethylhexyl, 2-methylhexyl, 2-propylhexyl, n-nonyl, isononyl, n-decyl, isodecil, n-undecyl, isoundecyl, n-dodecyl, isododecyl, n-tridecyl, isotridecyl, n- Tetradecyl, isotetradecyl, n-pentadecyl, isopentadecyl, n-hexadecyl, isohexadecyl, n-heptadecyl, isoheptadecyl, n-octadecyl, isooctadecyl, n-nonadecil, isononadecyl, n-icosyl, isoicosyl, cyclopentyl, cyclohexyl. , Cyclooctyl, cyclododecyl, benzyl, phenethyl, 2-phenylpropan-2-yl, styryl, cinnamyl, diphenylmethyl, triphenylmethyl and the like.
 一般式(1)のAr、ArおよびArが有する置換基の、置換基を有していてもよい炭素原子数6~20のアリール基としては、フェニル、p-メチルフェニル、o-メチルフェニル、p-tert-ブチルフェニル、p-メトキシフェニル、p-クロルフェニル、p-ニトロフェニル、p-シアノフェニル、o-ビフェニリル、m-ビフェニリル、p-ビフェニリル、α-ナフチル、β-ナフチル、1-アントリル、2-アントリル、9-アントリル、1-フェナントリル、2-フェナントリル、3-フェナントリル、4-フェナントリル、9-フェナントリル等が挙げられる。 Of the substituents of Ar 1 , Ar 2 and Ar 3 of the general formula (1), the aryl groups having 6 to 20 carbon atoms which may have a substituent include phenyl, p-methylphenyl and o-. Methylphenyl, p-tert-butylphenyl, p-methoxyphenyl, p-chlorophenyl, p-nitrophenyl, p-cyanophenyl, o-biphenylyl, m-biphenylyl, p-biphenylyl, α-naphthyl, β-naphthyl, Examples thereof include 1-anthryl, 2-anthryl, 9-anthryl, 1-phenyl, 2-phenyl, 3-phenyl, 4-phenyl, 9-phenyl and the like.
 一般式(1)中のAr、ArおよびArが有する置換基の、置換基を有していてもよいアミノ基の例を挙げると、無置換のアミノ基のほか、上記アルキル基または上記アリール基で置換されたアミノ基が挙げられ、具体的には、アミノ、メチルアミノ、エチルアミノ、n-プロピルアミノ、イソプロピルアミノ、シクロプロピルアミノ、n-ブチルアミノ、イソブチルアミノ、sec-ブチルアミノ、tert-ブチルアミノ、シクロブチルアミノ、1-ペンチルアミノ、2-ペンチルアミノ、3-ペンチルアミノ、イソペンチルアミノ、ネオペンチルアミノ、tert-ペンチルアミノ、シクロペンチルアミノ、1-ヘキシルアミノ、2-ヘキシルアミノ、3-ヘキシルアミノ、シクロヘキシルアミノ、1-メチル-n-ペンチルアミノ、1,1,2-トリメチル-n-プロピルアミノ、1,2,2-トリメチル-n-プロピルアミノ、3,3-ジメチル-n-ブチルアミノ、ジメチルアミノ、ジエチルアミノ、ジ-n-プロピルアミノ、ジイソプロピルアミノ、ジシクロプロピルアミノ、ジ-n-ブチルアミノ、ジイソブチルアミノ、ジ-sec-ブチルアミノ、ジ-tert-ブチルアミノ、ジシクロブチルアミノ、ジ-1-ペンチルアミノ、ジ-2-ペンチルアミノ、ジ-3-ペンチルアミノ、ジイソペンチルアミノ、ジ-ネオペンチルアミノ、ジ-tert-ペンチルアミノ、ジシクロペンチルアミノ、ジ-1-ヘキシルアミノ、ジ-2-ヘキシルアミノ、ジ-3-ヘキシルアミノ、ジシクロヘキシルアミノ、ジ-(1-メチル-n-ペンチル)アミノ、ジ-(1,1,2-トリメチル-n-プロピル)アミノ、ジ-(1,2,2-トリメチル-n-プロピル)アミノ、ジ-(3,3-ジメチル-n-ブチル)アミノ、メチル(エチル)アミノ、メチル(n-プロピル)アミノ、メチル(イソプロピル)アミノ、メチル(シクロプロピル)アミノ、メチル(n-ブチル)アミノ、メチル(イソブチル)アミノ、メチル(sec-ブチル)アミノ、メチル(tert-ブチル)アミノ、メチル(シクロブチル)アミノ、エチル(n-プロピル)アミノ、エチル(イソプロピル)アミノ、エチル(シクロプロピル)アミノ、エチル(n-ブチル)アミノ、エチル(イソブチル)アミノ、エチル(sec-ブチル)アミノ、エチル(tert-ブチル)アミノ、エチル(シクロブチル)アミノ、n-プロピル(イソプロピル)アミノ、n-プロピル(シクロプロピル)アミノ、n-プロピル(n-ブチル)アミノ、n-プロピル(イソブチル)アミノ、n-プロピル(sec-ブチル)アミノ、n-プロピル(tert-ブチル)アミノ、n-プロピル(シクロブチル)アミノ、イソプロピル(シクロプロピル)アミノ、イソプロピル(n-ブチル)アミノ、イソプロピル(イソブチル)アミノ、イソプロピル(sec-ブチル)アミノ、イソプロピル(tert-ブチル)アミノ、イソプロピル(シクロブチル)アミノ、シクロプロピル(n-ブチル)アミノ、シクロプロピル(イソブチル)アミノ、シクロプロピル(sec-ブチル)アミノ、シクロプロピル(tert-ブチル)アミノ、シクロプロピル(シクロブチル)アミノ、n-ブチル(イソブチル)アミノ、n-ブチル(sec-ブチル)アミノ、n-ブチル(tert-ブチル)アミノ、n-ブチル(シクロブチル)アミノ、イソブチル(sec-ブチル)アミノ、イソブチル(tert-ブチル)アミノ、イソブチル(シクロブチル)アミノ、sec-ブチル(tert-ブチル)アミノ、sec-ブチル(シクロブチル)アミノ、tert-ブチル(シクロブチル)アミノ、フェニルアミノ、ナフチルアミノ、p-メチルフェニルアミノ、o-メチルフェニルアミノ、p-tert-ブチルフェニルアミノ、p-メトキシフェニルアミノ、p-クロルフェニルアミノ、p-ニトロフェニルアミノ、p-シアノフェニルアミノ、o-ビフェニリルアミノ、m-ビフェニリルアミノ、p-ビフェニリルアミノ、α-ナフチルアミノ、β-ナフチルアミノ、1-アントリルアミノ、2-アントリルアミノ、9-アントリルアミノ、1-フェナントリルアミノ、2-フェナントリルアミノ、3-フェナントリルアミノ、4-フェナントリルアミノ、9-フェナントリルアミノ、ジフェニルアミノ、ジナフチルアミノ、フェニルナフチルアミノ、メチルフェニルアミノ、エチルフェニルアミノ、イソプロピルフェニルアミノ、sec-ブチルフェニルアミノ、tert-ブチルフェニルアミノ、n-ヘキシルフェニルアミノ、シクロヘキシルフェニルアミノ、メチルナフチルアミノ、エチルナフチルアミノ等が挙げられる。 Examples of amino groups that may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include the above-mentioned alkyl group or the above-mentioned alkyl group in addition to the unsubstituted amino group. Examples thereof include amino groups substituted with the above aryl groups, and specific examples thereof include amino, methylamino, ethylamino, n-propylamino, isopropylamino, cyclopropylamino, n-butylamino, isobutylamino, and sec-butylamino. , Tert-Butylamino, Cyclobutylamino, 1-Pentylamino, 2-Pentylamino, 3-Pentylamino, Isopentylamino, Neopentylamino, tert-Pentylamino, Cyclopentylamino, 1-Hexylamino, 2-Hexylamino , 3-Hexylamino, Cyclohexylamino, 1-Methyl-n-pentylamino, 1,1,2-trimethyl-n-propylamino, 1,2,2-trimethyl-n-propylamino, 3,3-dimethyl- n-Butylamino, dimethylamino, diethylamino, di-n-propylamino, diisopropylamino, dicyclopropylamino, di-n-butylamino, diisobutylamino, di-sec-butylamino, di-tert-butylamino, di Cyclobutylamino, di-1-pentylamino, di-2-pentylamino, di-3-pentylamino, diisopentylamino, di-neopentylamino, di-tert-pentylamino, dicyclopentylamino, di-1 -Hexylamino, di-2-hexylamino, di-3-hexylamino, dicyclohexylamino, di- (1-methyl-n-pentyl) amino, di- (1,1,2-trimethyl-n-propyl) amino , Di- (1,2,2-trimethyl-n-propyl) amino, di- (3,3-dimethyl-n-butyl) amino, methyl (ethyl) amino, methyl (n-propyl) amino, methyl (isopropyl) ) Amino, methyl (cyclopropyl) amino, methyl (n-butyl) amino, methyl (isobutyl) amino, methyl (sec-butyl) amino, methyl (tert-butyl) amino, methyl (cyclobutyl) amino, ethyl (n-) Propyl) amino, ethyl (isopropyl) amino, ethyl (cyclopropyl) amino, ethyl (n-butyl) amino, ethyl (isobutyl) amino, ethyl (sec-butyl) amino, ethyl (tert-butyl) amino, ethyl (cyclobutyl) ) Amino, n-Pro Pill (isopropyl) amino, n-propyl (cyclopropyl) amino, n-propyl (n-butyl) amino, n-propyl (isobutyl) amino, n-propyl (sec-butyl) amino, n-propyl (tert-butyl) ) Amino, n-propyl (cyclobutyl) amino, isopropyl (cyclopropyl) amino, isopropyl (n-butyl) amino, isopropyl (isobutyl) amino, isopropyl (sec-butyl) amino, isopropyl (tert-butyl) amino, isopropyl ( Cyclobutyl) amino, cyclopropyl (n-butyl) amino, cyclopropyl (isobutyl) amino, cyclopropyl (sec-butyl) amino, cyclopropyl (tert-butyl) amino, cyclopropyl (cyclobutyl) amino, n-butyl (isobutyl) ) Amino, n-butyl (sec-butyl) amino, n-butyl (tert-butyl) amino, n-butyl (cyclobutyl) amino, isobutyl (sec-butyl) amino, isobutyl (tert-butyl) amino, isobutyl (cyclobutyl) ) Amino, sec-butyl (tert-butyl) amino, sec-butyl (cyclobutyl) amino, tert-butyl (cyclobutyl) amino, phenylamino, naphthylamino, p-methylphenylamino, o-methylphenylamino, p-tert -Butylphenylamino, p-methoxyphenylamino, p-chlorophenylamino, p-nitrophenylamino, p-cyanophenylamino, o-biphenylylamino, m-biphenylylamino, p-biphenylylamino, α-naphthyl Amino, β-naphthylamino, 1-anthrylamino, 2-anthrylamino, 9-anthrylamino, 1-phenanthrylamino, 2-phenanthrylamino, 3-phenanthrylamino, 4-phenan Trillamino, 9-phenanthrilamino, diphenylamino, dinaphthylamino, phenylnaphthylamino, methylphenylamino, ethylphenylamino, isopropylphenylamino, sec-butylphenylamino, tert-butylphenylamino, n-hexylphenylamino , Cyclohexylphenylamino, methylnaphthylamino, ethylnaphthylamino and the like.
 一般式(1)中のAr、ArおよびArが有する置換基の、置換基を有していてもよいアミノカルボニル基としては、無置換のアミノカルボニル基のほか、上記アルキル基または上記アリール基で置換されたアミノカルボニル基が挙げられ、具体的には、アミノカルボニル、メチルアミノカルボニル、エチルアミノカルボニル、n-プロピルアミノカルボニル、イソプロピルアミノカルボニル、n-ブチルアミノカルボニル、イソブチルアミノカルボニル、sec-ブチルアミノカルボニル、tert-ブチルアミノカルボニル、1-ペンチルアミノカルボニル、2-ペンチルアミノカルボニル、3-ペンチルアミノカルボニル、i-ペンチルアミノカルボニル、ネオペンチルアミノカルボニル、tert-ペンチルアミノカルボニル、1-ヘキシルアミノカルボニル、2-ヘキシルアミノカルボニル、3-ヘキシルアミノカルボニル、シクロヘキシルアミノカルボニル、フェニルアミノカルボニル、ナフチルアミノカルボニル、p-メチルフェニルアミノカルボニル、o-メチルフェニルアミノカルボニル、p-tert-ブチルフェニルアミノカルボニル、p-メトキシフェニルアミノカルボニル、p-クロルフェニルアミノカルボニル、p-ニトロフェニルアミノカルボニル、p-シアノフェニルアミノカルボニル、o-ビフェニリルアミノカルボニル、m-ビフェニリルアミノカルボニル、p-ビフェニリルアミノカルボニル、α-ナフチルアミノカルボニル、β-ナフチルアミノカルボニル、1-アントリルアミノカルボニル、2-アントリルアミノカルボニル、9-アントリルアミノカルボニル、1-フェナントリルアミノカルボニル、2-フェナントリルアミノカルボニル、3-フェナントリルアミノカルボニル、4-フェナントリルアミノカルボニル、9-フェナントリルアミノカルボニル、ジメチルアミノカルボニル、ジエチルアミノカルボニル、ジ-n-プロピルアミノカルボニル、ジイソプロピルアミノカルボニル、ジシクロプロピルアミノカルボニル、ジ-n-ブチルアミノカルボニル、ジイソブチルアミノカルボニル、ジ-sec-ブチルアミノカルボニル、ジ-tert-ブチルアミノカルボニル、ジシクロブチルアミノカルボニル、ジ-1-ペンチルアミノカルボニル、ジ-2-ペンチルアミノカルボニル、ジ-3-ペンチルアミノカルボニル、ジイソペンチルアミノカルボニル、ジ-ネオペンチルアミノカルボニル、ジ-tert-ペンチルアミノカルボニル、ジシクロペンチルアミノカルボニル、ジ-1-ヘキシルアミノカルボニル、ジ-2-ヘキシルアミノカルボニル、ジ-3-ヘキシルアミノカルボニル、ジシクロヘキシルアミノカルボニル、ジ-(1-メチル-n-ペンチル)アミノカルボニル、ジ-(1,1,2-トリメチル-n-プロピル)アミノカルボニル、ジ-(1,2,2-トリメチル-n-プロピル)アミノカルボニル、ジ-(3,3-ジメチル-n-ブチル)アミノカルボニル、メチル(エチル)アミノカルボニル、メチル(n-プロピル)アミノカルボニル、メチル(イソプロピル)アミノカルボニル、メチル(シクロプロピル)アミノカルボニル、メチル(n-ブチル)アミノカルボニル、メチル(イソブチル)アミノカルボニル、メチル(sec-ブチル)アミノカルボニル、メチル(tert-ブチル)アミノカルボニル、メチル(シクロブチル)アミノカルボニル、エチル(n-プロピル)アミノカルボニル、エチル(イソプロピル)アミノカルボニル、エチル(シクロプロピル)アミノカルボニル、エチル(n-ブチル)アミノカルボニル、エチル(イソブチル)アミノカルボニル、エチル(sec-ブチル)アミノカルボニル、エチル(tert-ブチル)アミノカルボニル、エチル(シクロブチル)アミノカルボニル、n-プロピル(イソプロピル)アミノカルボニル、n-プロピル(シクロプロピル)アミノカルボニル、n-プロピル(n-ブチル)アミノカルボニル、n-プロピル(イソブチル)アミノカルボニル、n-プロピル(sec-ブチル)アミノカルボニル、n-プロピル(tert-ブチル)アミノカルボニル、n-プロピル(シクロブチル)アミノカルボニル、イソプロピル(シクロプロピル)アミノカルボニル、イソプロピル(n-ブチル)アミノカルボニル、イソプロピル(イソブチル)アミノカルボニル、イソプロピル(sec-ブチル)アミノカルボニル、イソプロピル(tert-ブチル)カルボニルアミノ、イソプロピル(シクロブチル)アミノカルボニル、シクロプロピル(n-ブチル)アミノカルボニル、シクロプロピル(イソブチル)アミノカルボニル、シクロプロピル(sec-ブチル)アミノカルボニル、シクロプロピル(tert-ブチル)アミノカルボニル、シクロプロピル(シクロブチル)アミノカルボニル、n-ブチル(イソブチル)アミノカルボニル、n-ブチル(sec-ブチル)アミノカルボニル、n-ブチル(tert-ブチル)アミノカルボニル、n-ブチル(シクロブチル)アミノカルボニル、イソブチル(sec-ブチル)アミノカルボニル、イソブチル(tert-ブチル)アミノカルボニル、イソブチル(シクロブチル)アミノカルボニル、sec-ブチル(tert-ブチル)アミノカルボニル、sec-ブチル(シクロブチル)アミノカルボニル、tert-ブチル(シクロブチル)アミノカルボニル、ジフェニルアミノカルボニル、ジナフチルアミノカルボニル、ジ(p-メチルフェニル)アミノカルボニル、フェニルナフチルアミノカルボニル、メチルフェニルアミノ、エチルフェニルアミノ、イソプロピルフェニルアミノ、sec-ブチルフェニルアミノ、tert-ブチルフェニルアミノ、n-ヘキシルフェニルアミノ、シクロヘキシルフェニルアミノ、メチルナフチルアミノ、エチルナフチルアミノ等が挙げられる。 As the aminocarbonyl group which may have a substituent of the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1), in addition to the unsubstituted aminocarbonyl group, the above alkyl group or the above. Examples thereof include aminocarbonyl groups substituted with aryl groups, and specific examples thereof include aminocarbonyl, methylaminocarbonyl, ethylaminocarbonyl, n-propylaminocarbonyl, isopropylaminocarbonyl, n-butylaminocarbonyl, isobutylaminocarbonyl, sec. -Butylaminocarbonyl, tert-butylaminocarbonyl, 1-pentylaminocarbonyl, 2-pentylaminocarbonyl, 3-pentylaminocarbonyl, i-pentylaminocarbonyl, neopentylaminocarbonyl, tert-pentylaminocarbonyl, 1-hexylamino Carbonyl, 2-hexylaminocarbonyl, 3-hexylaminocarbonyl, cyclohexylaminocarbonyl, phenylaminocarbonyl, naphthylaminocarbonyl, p-methylphenylaminocarbonyl, o-methylphenylaminocarbonyl, p-tert-butylphenylaminocarbonyl, p -Methoxyphenylaminocarbonyl, p-chlorophenylaminocarbonyl, p-nitrophenylaminocarbonyl, p-cyanophenylaminocarbonyl, o-biphenylylaminocarbonyl, m-biphenylylaminocarbonyl, p-biphenylylaminocarbonyl, α- Naftylaminocarbonyl, β-naphthylaminocarbonyl, 1-anthrylaminocarbonyl, 2-anthrylaminocarbonyl, 9-anthrylaminocarbonyl, 1-phenanthrylaminocarbonyl, 2-phenanthrylaminocarbonyl, 3-fe Nantrilaminocarbonyl, 4-phenanthrilaminocarbonyl, 9-phenanthrilaminocarbonyl, dimethylaminocarbonyl, diethylaminocarbonyl, di-n-propylaminocarbonyl, diisopropylaminocarbonyl, dicyclopropylaminocarbonyl, di-n- Butylaminocarbonyl, diisobutylaminocarbonyl, di-sec-butylaminocarbonyl, di-tert-butylaminocarbonyl, dicyclobutylaminocarbonyl, di-1-pentylaminocarbonyl, di-2-pentylaminocarbonyl, di-3- Pentylaminocarbonyl, diisopentylaminocarbo Nyl, di-neopentylaminocarbonyl, di-tert-pentylaminocarbonyl, dicyclopentylaminocarbonyl, di-1-hexylaminocarbonyl, di-2-hexylaminocarbonyl, di-3-hexylaminocarbonyl, dicyclohexylaminocarbonyl, Di- (1-methyl-n-pentyl) aminocarbonyl, di- (1,1,2-trimethyl-n-propyl) aminocarbonyl, di- (1,2,2-trimethyl-n-propyl) aminocarbonyl, Di- (3,3-dimethyl-n-butyl) aminocarbonyl, methyl (ethyl) aminocarbonyl, methyl (n-propyl) aminocarbonyl, methyl (isopropyl) aminocarbonyl, methyl (cyclopropyl) aminocarbonyl, methyl (n) -Butyl) aminocarbonyl, methyl (isobutyl) aminocarbonyl, methyl (sec-butyl) aminocarbonyl, methyl (tert-butyl) aminocarbonyl, methyl (cyclobutyl) aminocarbonyl, ethyl (n-propyl) aminocarbonyl, ethyl (isopropyl) ) Aminocarbonyl, ethyl (cyclopropyl) aminocarbonyl, ethyl (n-butyl) aminocarbonyl, ethyl (isobutyl) aminocarbonyl, ethyl (sec-butyl) aminocarbonyl, ethyl (tert-butyl) aminocarbonyl, ethyl (cyclobutyl) Aminocarbonyl, n-propyl (isopropyl) aminocarbonyl, n-propyl (cyclopropyl) aminocarbonyl, n-propyl (n-butyl) aminocarbonyl, n-propyl (isobutyl) aminocarbonyl, n-propyl (sec-butyl) Aminocarbonyl, n-propyl (tert-butyl) aminocarbonyl, n-propyl (cyclobutyl) aminocarbonyl, isopropyl (cyclopropyl) aminocarbonyl, isopropyl (n-butyl) aminocarbonyl, isopropyl (isobutyl) aminocarbonyl, isopropyl (sec) -Butyl) aminocarbonyl, isopropyl (tert-butyl) carbonylamino, isopropyl (cyclobutyl) aminocarbonyl, cyclopropyl (n-butyl) aminocarbonyl, cyclopropyl (isobutyl) aminocarbonyl, cyclopropyl (sec-butyl) aminocarbonyl, Cyclopropyl (tert-butyl) aminocarbonyl, cyclopropyl (cyclobutyl) aminocalc Bonil, n-butyl (isobutyl) aminocarbonyl, n-butyl (sec-butyl) aminocarbonyl, n-butyl (tert-butyl) aminocarbonyl, n-butyl (cyclobutyl) aminocarbonyl, isobutyl (sec-butyl) aminocarbonyl , Isobutyl (tert-butyl) aminocarbonyl, isobutyl (cyclobutyl) aminocarbonyl, sec-butyl (tert-butyl) aminocarbonyl, sec-butyl (cyclobutyl) aminocarbonyl, tert-butyl (cyclobutyl) aminocarbonyl, diphenylaminocarbonyl, Dinaphthylaminocarbonyl, di (p-methylphenyl) aminocarbonyl, phenylnaphthylaminocarbonyl, methylphenylamino, ethylphenylamino, isopropylphenylamino, sec-butylphenylamino, tert-butylphenylamino, n-hexylphenylamino, Cyclohexylphenylamino, methylnaphthylamino, ethylnaphthylamino and the like can be mentioned.
 一般式(1)中のAr、ArおよびArが有する置換基の、置換基を有していてもよい炭素原子数1~20のアルコキシ基としては、メトキシ、エトキシ、n-プロポキシ、イソプロポキシ、n-ブトキシ、イソブトキシ、sec-ブトキシ、tert-ブトキシ、n-ペンチルオキシ、イソペンチルオキシ、ネオペンチルオキシ、1,2-ジメチル-プロポキシ、n-ヘキシルオキシ、シクロヘキシルオキシ、1,3-ジメチルブトキシ、1-イソプロピルプロポキシ等が挙げられる。 Examples of the alkoxy group having 1 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include methoxy, ethoxy, and n-propoxy. Isopropoxy, n-butoxy, isobutoxy, sec-butoxy, tert-butoxy, n-pentyloxy, isopentyloxy, neopentyloxy, 1,2-dimethyl-propoxy, n-hexyloxy, cyclohexyloxy, 1,3- Examples thereof include dimethylbutoxy and 1-isopropylpropoxy.
 一般式(1)中のAr、ArおよびArが有する置換基の、置換基を有していてもよい炭素原子数6~20のアリールオキシ基としては、フェノキシ、ナフチルオキシ、p-メチルフェノキシ、o-メチルフェノキシ、p-tert-ブチルフェノキシ、p-メトキシフェノキシ、p-クロルフェニノキシ、p-ニトロフェノキシ、p-シアノフェノキシ、o-ビフェニリルオキシ、m-ビフェニリルオキシ、p-ビフェニリルオキシ、α-ナフチルオキシ、β-ナフチルオキシ、1-アントリルオキシ、2-アントリルオキシ、9-アントリルオキシ、1-フェナントリルオキシ、2-フェナントリルオキシ、3-フェナントリルオキシ、4-フェナントリルオキシ、9-フェナントリルオキシ等が挙げられる。 Among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1), the aryloxy groups having 6 to 20 carbon atoms which may have a substituent include phenoxy, naphthyloxy and p-. Methylphenoxy, o-methylphenoxy, p-tert-butylphenoxy, p-methoxyphenoxy, p-chlorpheninoxy, p-nitrophenoxy, p-cyanophenoxy, o-biphenylyloxy, m-biphenylyloxy, p -Biphenylyloxy, α-naphthyloxy, β-naphthyloxy, 1-anthryloxy, 2-antryloxy, 9-antryloxy, 1-phenanthryloxy, 2-phenanthryloxy, 3-fe Examples thereof include nantriloxy, 4-phenanthryloxy, 9-phenanthryloxy and the like.
 一般式(1)中のAr、ArおよびArが有する置換基の、置換基を有していてもよい炭素原子数1~20のアルキルチオ基としては、メチルチオ基、エチルチオ基、n-プロピルチオ基、イソプロピルチオ基、n-ブチルチオ基、イソブチルチオ基、sec-ブチルチオ基、tert-ブチルチオ基等が挙げられる。 Examples of the alkylthio group having 1 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include methylthio group, ethylthio group and n-. Examples thereof include a propylthio group, an isopropylthio group, an n-butylthio group, an isobutylthio group, a sec-butylthio group, a tert-butylthio group and the like.
 一般式(1)中のAr、ArおよびArが有する置換基の、置換基を有していてもよい炭素原子数2~20のアルキルカルボニル基としては、メチルカルボニル(アセチルともいう)、エチルカルボニル、n-プロピルカルボニル、イソプロピルカルボニル、n-ブチルカルボニル、イソブチルカルボニル、sec-ブチルカルボニル、tert-ブチルカルボニル、1-ペンチルカルボニル、2-ペンチルカルボニル、3-ペンチルカルボニル、イソペンチルカルボニル、ネオペンチルカルボニル、tert-ペンチルカルボニル、1-ヘキシルカルボニル、2-ヘキシルカルボニル、3-ヘキシルカルボニル、シクロヘキシルカルボニル等が挙げられる。 The alkylcarbonyl group having 2 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) is methylcarbonyl (also referred to as acetyl). , Ethylcarbonyl, n-propylcarbonyl, isopropylcarbonyl, n-butylcarbonyl, isobutylcarbonyl, sec-butylcarbonyl, tert-butylcarbonyl, 1-pentylcarbonyl, 2-pentylcarbonyl, 3-pentylcarbonyl, isopentylcarbonyl, neo Examples thereof include pentylcarbonyl, tert-pentylcarbonyl, 1-hexylcarbonyl, 2-hexylcarbonyl, 3-hexylcarbonyl, cyclohexylcarbonyl and the like.
 一般式(1)中のAr、ArおよびArが有する置換基の、置換基を有していてもよい炭素原子数7~20のアリールカルボニル基としては、ベンゾイル、p-メチルベンゾイル、p-tert-ブチルベンゾイル、p-メトキシベンゾイル、p-クロルベンゾイル、p-ニトロベンゾイル、p-シアノベンゾイル、o-ビフェニリルカルボニル、m-ビフェニリルカルボニル、p-ビフェニリルカルボニル、α-ナフチルカルボニル、β-ナフチルカルボニル、1-アントリルカルボニル、2-アントリルカルボニル、9-アントリルカルボニル、1-フェナントリルカルボニル、2-フェナントリルカルボニル、3-フェナントリルカルボニル、4-フェナントリルカルボニル、9-フェナントリルカルボニル等が挙げられる。 Examples of the arylcarbonyl group having 7 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include benzoyl and p-methylbenzoyl. p-tert-butylbenzoyl, p-methoxybenzoyl, p-chlorbenzoyl, p-nitrobenzoyl, p-cyanobenzoyl, o-biphenylylcarbonyl, m-biphenylylcarbonyl, p-biphenylylcarbonyl, α-naphthylcarbonyl, β-naphthylcarbonyl, 1-anthrylcarbonyl, 2-anthrylcarbonyl, 9-anthrylcarbonyl, 1-phenanthrylcarbonyl, 2-phenanthrylcarbonyl, 3-phenanthrylcarbonyl, 4-phenanthrylcarbonyl , 9-Phenantril carbonyl and the like.
 一般式(1)中のAr、ArおよびArが有する置換基の、置換基を有していてもよい炭素原子数2~20のアルキルカルボニルオキシ基としては、メチルカルボニルオキシ、エチルカルボニルオキシ、n-プロピルカルボニルオキシ、イソプロピルカルボニルオキシ、n-ブチルカルボニルオキシ、イソブチルカルボニルオキシ、sec-ブチルカルボニルオキシ、tert-ブチルカルボニルオキシ、ペンチルカルボニルオキシ、ヘキシルカルボニルオキシ、シクロヘキシルカルボニルオキシ、ヘプチルカルボニルオキシ、ヘプタン-3-イルカルボニルオキシ等が挙げられる。 Examples of the alkylcarbonyloxy group having 2 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) are methylcarbonyloxy and ethylcarbonyl. Oxy, n-propylcarbonyloxy, isopropylcarbonyloxy, n-butylcarbonyloxy, isobutylcarbonyloxy, sec-butylcarbonyloxy, tert-butylcarbonyloxy, pentylcarbonyloxy, hexylcarbonyloxy, cyclohexylcarbonyloxy, heptylcarbonyloxy, Examples thereof include heptane-3-ylcarbonyloxy.
 一般式(1)中のAr、ArおよびArが有する置換基の、置換基を有していてもよい炭素原子数7~20のアリールカルボニルオキシ基としては、ベンゾイルオキシ、p-メチルベンゾイルオキシ、p-tert-ブチルベンゾイルオキシ、p-メトキシベンゾイルオキシ、p-クロルベンゾイルオキシ、p-ニトロベンゾイルオキシ、p-シアノベンゾイルオキシ、o-ビフェニリルカルボニルオキシ、m-ビフェニリルカルボニルオキシ、p-ビフェニリルカルボニルオキシ、α-ナフチルカルボニルオキシ、β-ナフチルカルボニルオキシ、1-アントリルカルボニルオキシ、2-アントリルカルボニルオキシ、9-アントリルカルボニルオキシ、1-フェナントリルカルボニルオキシ、2-フェナントリルカルボニルオキシ、3-フェナントリルカルボニルオキシ、4-フェナントリルカルボニルオキシ、9-フェナントリルカルボニルオキシ等が挙げられる。 Benzoyloxy and p-methyl are examples of arylcarbonyloxy groups having 7 to 20 carbon atoms which may have substituents among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1). Benzoyloxy, p-tert-butylbenzoyloxy, p-methoxybenzoyloxy, p-chlorobenzoyloxy, p-nitrobenzoyloxy, p-cyanobenzoyloxy, o-biphenylylcarbonyloxy, m-biphenylylcarbonyloxy, p -Biphenylylcarbonyloxy, α-naphthylcarbonyloxy, β-naphthylcarbonyloxy, 1-anthrylcarbonyloxy, 2-anthrylcarbonyloxy, 9-anthrylcarbonyloxy, 1-phenanthrylcarbonyloxy, 2-fe Examples thereof include nantrilcarbonyloxy, 3-phenanthrylcarbonyloxy, 4-phenanthrylcarbonyloxy, 9-phenanthrylcarbonyloxy and the like.
 一般式(1)中のAr、ArおよびArが有する置換基の、置換基を有していてもよい炭素原子数2~20のアルコキシカルボニル基としては、メトキシカルボニル、エトキシカルボニル、n-プロポキシカルボニル、イソプロポキシカルボニル、n-ブトキシカルボニル、イソブトキシカルボニル、sec-ブトキシカルボニル、tert-ブトキシカルボニル、1-ペンチルオキシカルボニル、2-ペンチルオキシカルボニル、3-ペンチルオキシカルボニル、イソペンチルオキシカルボニル、ネオペンチルオキシカルボニル、tert-ペンチルオキシカルボニル、1-ヘキシルオキシカルボニル、2-ヘキシルオキシカルボニル、3-ヘキシルオキシカルボニル、シクロヘキシルオキシカルボニル等が挙げられる。 Examples of the alkoxycarbonyl group having 2 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include methoxycarbonyl, ethoxycarbonyl and n. -Propoxycarbonyl, isopropoxycarbonyl, n-butoxycarbonyl, isobutoxycarbonyl, sec-butoxycarbonyl, tert-butoxycarbonyl, 1-pentyloxycarbonyl, 2-pentyloxycarbonyl, 3-pentyloxycarbonyl, isopentyloxycarbonyl, Examples thereof include neopentyloxycarbonyl, tert-pentyloxycarbonyl, 1-hexyloxycarbonyl, 2-hexyloxycarbonyl, 3-hexyloxycarbonyl, cyclohexyloxycarbonyl and the like.
 一般式(1)中のAr、ArおよびArが有する置換基の、置換基を有していてもよい炭素原子数7~20のアリールオキシカルボニル基としては、フェノキシカルボニル、p-メチルフェノキシカルボニル、ナフチルオキシカルボニル、ビフェニリルオキシカルボニル、アントリルオキシカルボニル、フェナントリルオキシカルボニル等が挙げられる。 Examples of the aryloxycarbonyl group having 7 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include phenoxycarbonyl and p-methyl. Examples thereof include phenoxycarbonyl, naphthyloxycarbonyl, biphenylyloxycarbonyl, anthryloxycarbonyl, phenanthryloxycarbonyl and the like.
 一般式(1)中のAr、ArおよびArが有する置換基の、置換基を有していてもよい炭素原子数2~20のアルキルカルボニルアミノ基としては、メチルカルボニルアミノ、エチルカルボニルアミノ、n-プロピルカルボニルアミノ、イソプロピルカルボニルアミノ、n-ブチルカルボニルアミノ、イソブチルカルボニルアミノ、sec-ブチルカルボニルアミノ、tert-ブチルカルボニルアミノ、1-ペンチルカルボニルアミノ、2-ペンチルカルボニルアミノ、3-ペンチルカルボニルアミノ、イソペンチルカルボニルアミノ、ネオペンチルカルボニルアミノ、tert-ペンチルカルボニルアミノ、1-ヘキシルカルボニルアミノ、2-ヘキシルカルボニルアミノ、3-ヘキシルカルボニルアミノ、シクロヘキシルカルボニルアミノ等が挙げられる。 Examples of the alkylcarbonylamino group having 2 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include methylcarbonylamino and ethylcarbonyl. Amino, n-propylcarbonylamino, isopropylcarbonylamino, n-butylcarbonylamino, isobutylcarbonylamino, sec-butylcarbonylamino, tert-butylcarbonylamino, 1-pentylcarbonylamino, 2-pentylcarbonylamino, 3-pentylcarbonyl Examples thereof include amino, isopentylcarbonylamino, neopentylcarbonylamino, tert-pentylcarbonylamino, 1-hexylcarbonylamino, 2-hexylcarbonylamino, 3-hexylcarbonylamino and cyclohexylcarbonylamino.
 一般式(1)中のAr、ArおよびArが有する置換基の、置換基を有していてもよい炭素原子数7~20のアリールカルボニルアミノ基としては、フェニルカルボニルアミノ、ナフチルカルボニルアミノ、p-メチルフェニルカルボニルアミノ、o-メチルフェニルカルボニルアミノ、p-tert-ブチルフェニルカルボニルアミノ、p-メトキシフェニルカルボニルアミノ、p-クロルフェニルカルボニルアミノ、p-ニトロフェニルカルボニルアミノ、p-シアノフェニルカルボニルアミノ、o-ビフェニリルカルボニルアミノ、m-ビフェニリルカルボニルアミノ、p-ビフェニリルカルボニルアミノ、α-ナフチルカルボニルアミノ、β-ナフチルカルボニルアミノ、1-アントリルカルボニルアミノ、2-アントリルカルボニルアミノ、9-アントリルカルボニルアミノ、1-フェナントリルカルボニルアミノ、2-フェナントリルカルボニルアミノ、3-フェナントリルカルボニルアミノ、4-フェナントリルカルボニルアミノ、9-フェナントリルカルボニルアミノ等が挙げられる。 Examples of the arylcarbonylamino group having 7 to 20 carbon atoms which may have a substituent among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1) include phenylcarbonylamino and naphthylcarbonyl. Amino, p-methylphenylcarbonylamino, o-methylphenylcarbonylamino, p-tert-butylphenylcarbonylamino, p-methoxyphenylcarbonylamino, p-chlorophenylcarbonylamino, p-nitrophenylcarbonylamino, p-cyanophenyl Carbonylamino, o-biphenylylcarbonylamino, m-biphenylylcarbonylamino, p-biphenylylcarbonylamino, α-naphthylcarbonylamino, β-naphthylcarbonylamino, 1-anthrylcarbonylamino, 2-anthrylcarbonylamino, Examples thereof include 9-anthrylcarbonylamino, 1-phenanthrylcarbonylamino, 2-phenanthrylcarbonylamino, 3-phenanthrylcarbonylamino, 4-phenanthrylcarbonylamino, 9-phenanthrylcarbonylamino and the like. ..
 一般式(1)中のAr、ArおよびArが有する置換基の、置換基を有していてもよい炭素原子数2~20の複素環基としては、ピリジル、ピリミジル、フリル、チエニル、テトラヒドロフリル、ジオキソラニル、ベンゾオキサゾール-2-イル、テトラヒドロピラニル、ピロリジル、イミダゾリジル、ピラゾリジル、チアゾリジル、イソチアゾリジル、オキサゾリジル、イソオキサゾリジル、ピペリジル、ピペラジル、モルホリニル等の5~7員複素環等が挙げられる。 Among the substituents of Ar 1 , Ar 2 and Ar 3 in the general formula (1), the heterocyclic groups having 2 to 20 carbon atoms which may have a substituent include pyridyl, pyrimidyl, furyl and thienyl. , Tetrahydrofuryl, dioxolanyl, benzoxazole-2-yl, tetrahydropyranyl, pyrrolidyl, imidazolidyl, pyrazolysyl, thiazolidyl, isothiazolydyl, oxazolidyl, isooxazolydyl, piperidyl, piperazyl, morpholinyl and the like. Be done.
 本実施形態の透明化剤に含まれる(A)一般式(1)で表されるトリアジン化合物においては、Ar、ArおよびArのうち少なくとも1つが、カルボニル基を含む置換基を有することが好ましい。この場合、成形品にさらに優れた透明性を付与できる。 In the triazine compound represented by (A) general formula (1) contained in the clearing agent of the present embodiment, at least one of Ar 1 , Ar 2 and Ar 3 has a substituent containing a carbonyl group. Is preferable. In this case, it is possible to impart even better transparency to the molded product.
 カルボニル基を含む置換基の例を挙げると、カルボキシ基、アミノカルボニル基、炭素原子数2~20のアルキルカルボニル基、炭素原子数7~20のアリールカルボニル基、炭素原子数2~20のアルキルカルボニルオキシ基、炭素原子数7~20のアリールカルボニルオキシ基、炭素原子数2~20のアルコキシカルボニル基、炭素原子数7~20のアリールオキシカルボニル基、炭素原子数2~20アルキルアミノカルボニル基、炭素原子数7~20のアリールアミノカルボニル基、炭素原子数3~20のジアルキルアミノカルボニル基、炭素原子数13~20のジアリールアミノカルボニル基、炭素原子数8~20のアルキルアリールアミノカルボニル基、炭素原子数2~20のアルキルカルボニルアミノ基、炭素原子数7~20のアリールカルボニルアミノ基等が挙げられ、これらは前述の置換基で置換されていてもよい。また、カルボキシ基は塩を形成していてもよい。 Examples of substituents containing a carbonyl group include a carboxy group, an aminocarbonyl group, an alkylcarbonyl group having 2 to 20 carbon atoms, an arylcarbonyl group having 7 to 20 carbon atoms, and an alkylcarbonyl group having 2 to 20 carbon atoms. Oxy group, arylcarbonyloxy group with 7 to 20 carbon atoms, alkoxycarbonyl group with 2 to 20 carbon atoms, aryloxycarbonyl group with 7 to 20 carbon atoms, alkylaminocarbonyl group with 2 to 20 carbon atoms, carbon Arylaminocarbonyl group with 7 to 20 atoms, dialkylaminocarbonyl group with 3 to 20 carbon atoms, diarylaminocarbonyl group with 13 to 20 carbon atoms, alkylarylaminocarbonyl group with 8 to 20 carbon atoms, carbon atom Examples thereof include an alkylcarbonylamino group having a number of 2 to 20, an arylcarbonylamino group having a carbon atom number of 7 to 20, and the like, which may be substituted with the above-mentioned substituent. Further, the carboxy group may form a salt.
 カルボニル基を含む置換基の中でも、成形品にさらに優れた透明性を付与する観点から、カルボキシ基、アミノカルボニル基、炭素原子数2~20のアルキルアミノカルボニル基、炭素原子数7~20のアリールアミノカルボニル基、炭素原子数3~20のジアルキルアミノカルボニル基、炭素原子数13~20のジアリールアミノカルボニル基、炭素原子数8~20のアルキルアリールアミノカルボニル基が好ましく、カルボキシ基、アミノカルボニル基がより好ましく、アミノカルボニル基が特に好ましい。 Among the substituents containing a carbonyl group, a carboxy group, an aminocarbonyl group, an alkylaminocarbonyl group having 2 to 20 carbon atoms, and an aryl having 7 to 20 carbon atoms from the viewpoint of imparting more excellent transparency to the molded product. An aminocarbonyl group, a dialkylaminocarbonyl group having 3 to 20 carbon atoms, a diarylaminocarbonyl group having 13 to 20 carbon atoms, and an alkylarylaminocarbonyl group having 8 to 20 carbon atoms are preferable, and a carboxy group and an aminocarbonyl group are used. More preferably, an aminocarbonyl group is particularly preferable.
 成形品にさらに優れた透明性を付与する観点から、本実施形態の透明化剤に含まれる(A)一般式(1)で表されるトリアジン化合物においては、Ar、ArおよびArのうち、いずれか一つのみがカルボニル基を含む置換基を有することが好ましい。また、本実施形態の透明化剤に含まれる(A)一般式(1)で表されるトリアジン化合物においては、Ar、ArおよびArのうち、いずれか一つがカルボニル基を含む置換基を有し、残りの二つがカルボニル基を含まない置換基を有することがより好ましい。 From the viewpoint of imparting more excellent transparency to the molded product, the triazine compound represented by the general formula (1) contained in the clearing agent of the present embodiment includes Ar 1 , Ar 2 and Ar 3 . Of these, it is preferable that only one of them has a substituent containing a carbonyl group. Further, in the triazine compound represented by the general formula (1) (A) contained in the clearing agent of the present embodiment , any one of Ar 1 , Ar 2 and Ar 3 is a substituent containing a carbonyl group. It is more preferable that the remaining two have a substituent containing no carbonyl group.
 ここで、カルボニル基を含まない置換基としては、成形品にさらに優れた透明性を付与する観点から、置換基を有していてもよい炭素原子数1~20のアルキル基または置換基を有していてもよい炭素原子数6~20のアリール基が好ましく、炭素原子数1~8のアルキル基または炭素原子数6~12のアリール基がより好ましく、メチル基、エチル基、n-プロピル基、シクロヘキシル基、置換基を有していてもよいフェニル基がさらに好ましく、n-プロピル基、フェニル基またはシクロヘキシル基がさらに一層好ましい。 Here, as the substituent containing no carbonyl group, an alkyl group having 1 to 20 carbon atoms or a substituent which may have a substituent may be used from the viewpoint of imparting more excellent transparency to the molded product. It is preferably an aryl group having 6 to 20 carbon atoms, more preferably an alkyl group having 1 to 8 carbon atoms or an aryl group having 6 to 12 carbon atoms, and a methyl group, an ethyl group or an n-propyl group. , A phenyl group which may have a cyclohexyl group or a substituent is further preferable, and an n-propyl group, a phenyl group or a cyclohexyl group is even more preferable.
 本実施形態の透明化剤に含まれる(A)一般式(1)で表されるトリアジン化合物の具体例としては、例えば、下記の化合物No.1~No.61が挙げられる。これらの中では、成形品に優れた透明性を付与する観点から、化合物No.6、化合物No.39、化合物No.49、化合物No.50、化合物No.58、化合物No.59、化合物No.60、化合物No.61のトリアジン化合物が好ましく、化合物No.6、化合物No.49、化合物No.59、化合物No.60、化合物No.61のトリアジン化合物がより好ましい。 Specific examples of the triazine compound represented by (A) general formula (1) contained in the clearing agent of the present embodiment include, for example, the following compound No. 1 to No. 61 is mentioned. Among these, from the viewpoint of imparting excellent transparency to the molded product, Compound No. 6. Compound No. 39, Compound No. 49, Compound No. 50, Compound No. 58, Compound No. 59, Compound No. 60, Compound No. The triazine compound of 61 is preferable, and the compound No. 6. Compound No. 49, Compound No. 59, Compound No. 60, Compound No. 61 triazine compounds are more preferred.
Figure JPOXMLDOC01-appb-I000023
Figure JPOXMLDOC01-appb-I000024
Figure JPOXMLDOC01-appb-I000025
Figure JPOXMLDOC01-appb-I000026
Figure JPOXMLDOC01-appb-I000027
Figure JPOXMLDOC01-appb-I000028
Figure JPOXMLDOC01-appb-I000029
Figure JPOXMLDOC01-appb-I000030
Figure JPOXMLDOC01-appb-I000031
Figure JPOXMLDOC01-appb-I000032
Figure JPOXMLDOC01-appb-I000033
Figure JPOXMLDOC01-appb-I000023
Figure JPOXMLDOC01-appb-I000024
Figure JPOXMLDOC01-appb-I000025
Figure JPOXMLDOC01-appb-I000026
Figure JPOXMLDOC01-appb-I000027
Figure JPOXMLDOC01-appb-I000028
Figure JPOXMLDOC01-appb-I000029
Figure JPOXMLDOC01-appb-I000030
Figure JPOXMLDOC01-appb-I000031
Figure JPOXMLDOC01-appb-I000032
Figure JPOXMLDOC01-appb-I000033
 一般式(1)で表されるトリアジン化合物の製造方法としては、例えば、有機溶媒下でシアヌル酸クロリドを原料とし、それぞれ1当量のAr、Ar、Arに対応するフェノール化合物をそれぞれ1当量の塩基(トリエチルアミン、水酸化ナトリウム等)存在下で順次反応させる方法等が挙げられる。 As a method for producing the triazine compound represented by the general formula (1), for example, cyanuric chloride is used as a raw material in an organic solvent, and 1 equivalent of each of the phenol compounds corresponding to Ar 1 , Ar 2 and Ar 3 is used. Examples thereof include a method of sequentially reacting in the presence of an equivalent amount of base (triethylamine, sodium hydroxide, etc.).
 一般式(2)における炭素原子数1~4のアルキル基としては、メチル基、エチル基、プロピル基、n-ブチル基、イソブチル基、sec-ブチル基、tert-ブチル基が挙げられる。また、炭素原子数1~4のアルコキシ基としては、メトキシ基、エトキシ基、プロポキシ基、n-ブチルオキシ基、イソブチルオキシ基、sec-ブチルオキシ基、tert-ブチルオキシ基が挙げられる。 Examples of the alkyl group having 1 to 4 carbon atoms in the general formula (2) include a methyl group, an ethyl group, a propyl group, an n-butyl group, an isobutyl group, a sec-butyl group and a tert-butyl group. Examples of the alkoxy group having 1 to 4 carbon atoms include a methoxy group, an ethoxy group, a propoxy group, an n-butyloxy group, an isobutyloxy group, a sec-butyloxy group and a tert-butyloxy group.
 一般式(2)における炭素原子数3~6のアルキレン基としては、例えばプロピレン基、ブチレン基、ペンチレン基、ヘキシレン基などが挙げられる。また、炭素原子数1~4のアルキレンジオキシ基としては、例えばメチレンジオキシ基、エチレンジオキシ基、プロピレンジオキシ基、ブチレンジオキシ基などが挙げられる。 Examples of the alkylene group having 3 to 6 carbon atoms in the general formula (2) include a propylene group, a butylene group, a pentylene group, and a hexylene group. Examples of the alkylenedioxy group having 1 to 4 carbon atoms include a methylenedioxy group, an ethylenedioxy group, a propylenedioxy group, and a butylenedioxy group.
 一般式(2)におけるハロゲン原子としては、フッ素原子、塩素原子、臭素原子、ヨウ素原子が挙げられる。 Examples of the halogen atom in the general formula (2) include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom.
 本実施形態の透明化剤に含まれる(B)一般式(2)で表されるアセタール化合物としては、R、R、R、RおよびRがそれぞれ独立に水素原子または炭素原子数1~4のアルキル基であり、Xが-CH(OH)-基であるものが好ましい。 As the acetal compound represented by the general formula (2) contained in the clearing agent of the present embodiment, R 1 , R 2 , R 3 , R 4 and R 5 are independently hydrogen atoms or carbon atoms, respectively. It is preferably an alkyl group having the number 1 to 4, and X is a −CH (OH) − group.
 本実施形態の透明化剤に含まれる(B)一般式(2)で表されるアセタール化合物の具体例としては、例えば、下記の化合物No.62~No.65などが挙げられる。これらの中では、成形品にさらに優れた透明性を付与する観点から、化合物No.62、化合物No.63および化合物No.64で表されるアセタール化合物が好ましい。 Specific examples of the acetal compound represented by the general formula (2) contained in the clearing agent of the present embodiment include the following compound No. 62-No. 65 and the like can be mentioned. Among these, from the viewpoint of imparting more excellent transparency to the molded product, Compound No. 62, Compound No. 63 and compound No. The acetal compound represented by 64 is preferable.
Figure JPOXMLDOC01-appb-I000034
Figure JPOXMLDOC01-appb-I000034
 一般式(2)で表されるアセタール化合物の製造方法としては、例えばソルビトールなどのアルジトール化合物とアリールアルデヒドとを、酸触媒の存在下、脱水縮合させる方法などが挙げられる。 Examples of the method for producing the acetal compound represented by the general formula (2) include a method of dehydrating and condensing an alditor compound such as sorbitol and arylaldehyde in the presence of an acid catalyst.
 本実施形態の透明化剤に含まれる(B)一般式(2)で表されるアセタール化合物のうち、市販されているものとしては、例えば、新日本理化社製のゲルオールD(商品名)、ゲルオールMD(商品名)、ゲルオールDXR(商品名)、ゲルオールE-200(商品名)、ゲルオールMD-LM30G(商品名)、RiKAFAST P1(商品名)、ミリケン・アンド・カンパニー社製のミラッド3988(商品名)、ミラッド3988i(商品名)、ミラッドNX-8000(商品名)、ミラッドNX-8000J(商品名)などが挙げられる。 Among the acetal compounds represented by the general formula (2) (B) contained in the clearing agent of the present embodiment, commercially available products include, for example, Gelol D (trade name) manufactured by Shin Nihon Rika Co., Ltd. Gelol MD (trade name), Gelol DXR (trade name), Gelol E-200 (trade name), Gelol MD-LM30G (trade name), RiKAFAST P1 (trade name), Mirad 3988 manufactured by Milliken & Company (trade name) (Product name), Mirad 3988i (trade name), Mirad NX-8000 (trade name), Mirad NX-8000J (trade name), and the like.
 上述したように、(A)トリアジン化合物の含有量(質量部)と(B)アセタール化合物の含有量(質量部)との比(A)/(B)は1/99~99/1である。成形品により優れた透明性を付与する観点から、(A)/(B)の値は10/90以上であることが好ましく、25/75以上であることがより好ましい。また、同様の観点から、(A)/(B)の値は90/10以下であることが好ましく、75/25以下であることがより好ましい。 As described above, the ratio (A) / (B) of the content (parts by mass) of the (A) triazine compound to the content (parts by mass) of the (B) acetal compound is 1/99 to 99/1. .. From the viewpoint of imparting more excellent transparency to the molded product, the values of (A) / (B) are preferably 10/90 or more, and more preferably 25/75 or more. From the same viewpoint, the value of (A) / (B) is preferably 90/10 or less, and more preferably 75/25 or less.
 本実施形態の透明化剤には、(A)トリアジン化合物および(B)アセタール化合物に加え、さらに(A)トリアジン化合物および(B)アセタール化合物以外の化合物であって、ポリオレフィン系樹脂に透明性を付与する機能を備えるものが含まれていてもよい。このような化合物としては、例えば、ナトリウム-2,2’-メチレンビス(4,6-ジ-tert-ブチルフェニル)ホスフェート、安息香酸ナトリウム、4-tert-ブチル安息香酸アルミニウム塩、アジピン酸ナトリウム、2ナトリウムビシクロ[2.2.1]ヘプタン-2,3-ジカルボキシレート、カルシウムシクロヘキサン-1,2-ジカルボキシレート等のカルボン酸金属塩、N,N’,N”-トリス[2-メチルシクロヘキシル]-1,2,3-プロパントリカルボキシアミド、N,N’,N”-トリシクロヘキシル-1,3,5-ベンゼントリカルボキシアミド、N,N’-ジシクロヘキシルナフタレンジカルボキシアミド、1,3,5-トリ(ジメチルイソプロポイルアミノ)ベンゼン等のアミド化合物等が挙げられる。透明化剤に(A)トリアジン化合物および(B)アセタール化合物以外の化合物であって、ポリオレフィン系樹脂に透明性を付与する機能を備えるものが含まれる場合、この化合物の含有量は、(A)トリアジン化合物の含有量および(B)アセタール化合物の含有量の合計100質量部に対して25質量部以下であることが好ましく、10質量部以下であることがより好ましく、1質量部以下であることがさらに好ましい。また、この化合物の含有量は、(A)トリアジン化合物の含有量および(B)アセタール化合物の含有量の合計100質量部に対して0.1質量部以上であればよい。 The clearing agent of the present embodiment is a compound other than (A) triazine compound and (B) acetal compound, as well as (A) triazine compound and (B) acetal compound, and makes the polyolefin resin transparent. Those having a function to be given may be included. Examples of such compounds include sodium-2,2'-methylenebis (4,6-di-tert-butylphenyl) phosphate, sodium benzoate, 4-tert-butyl benzoate aluminum salt, sodium adipate, 2 Carboxylic acid metal salts such as sodium bicyclo [2.2.1] heptane-2,3-dicarboxylate, calciumcyclohexane-1,2-dicarboxylate, N, N', N "-tris [2-methylcyclohexyl" ] -1,2,3-Propanetricarboxyamide, N, N', N "-tricyclohexyl-1,3,5-benzenetricarboxyamide, N, N'-dicyclohexylnaphthalenedicarboxyamide, 1,3 Examples thereof include amide compounds such as 5-tri (dimethylisopropoilamino) benzene. When the clearing agent contains a compound other than the (A) triazine compound and the (B) acetal compound having a function of imparting transparency to the polyolefin-based resin, the content of this compound is (A). The total content of the triazine compound and the content of the (B) acetal compound is preferably 25 parts by mass or less, more preferably 10 parts by mass or less, and 1 part by mass or less. Is even more preferable. The content of this compound may be 0.1 part by mass or more with respect to 100 parts by mass in total of (A) the content of the triazine compound and (B) the content of the acetal compound.
 本実施形態の透明化剤には、さらにフェノール系酸化防止剤、リン系酸化防止剤、硫黄系酸化防止剤、その他の酸化防止剤、ヒンダードアミン化合物、紫外線吸収剤、難燃剤、難燃助剤、滑剤、充填剤、ハイドロタルサイト類、脂肪酸金属塩、帯電防止剤、蛍光増白剤、顔料、染料等の各種添加剤が含まれていてもよい。 The clearing agent of the present embodiment further includes a phenol-based antioxidant, a phosphorus-based antioxidant, a sulfur-based antioxidant, other antioxidants, a hindered amine compound, an ultraviolet absorber, a flame retardant, and a flame retardant aid. Various additives such as lubricants, fillers, hydrotalcites, fatty acid metal salts, antistatic agents, fluorescent whitening agents, pigments and dyes may be contained.
 フェノール系酸化防止剤としては、例えば、2,6-ジ-tert-ブチル-4-エチルフェノール、2-tert-ブチル-4,6-ジメチルフェノール、スチレン化フェノール、2,2’-メチレンビス(4-エチル-6-tert-ブチルフェノール)、2,2’-チオビス-(6-tert-ブチル-4-メチルフェノール)、2,2’-チオジエチレンビス[3-(3,5-ジ-tert-ブチル-4-ヒドロキシフェニル)プロピオネート]、2-メチル-4,6-ビス(オクチルスルファニルメチル)フェノール、2,2’-イソブチリデンビス(4,6-ジメチルフェノール)、イソオクチル-3-(3,5-ジ-tert-ブチル-4-ヒドロキシフェニル)プロピオネート、N,N’-ヘキサン-1,6-ジイルビス[3-(3,5-ジ-tert-ブチル-4-ヒドロキシフェニル)プロピオンアミド]、2,2’-オキサミド-ビス[エチル-3-(3,5-ジ-tert-ブチル-4-ヒドロキシフェニル)プロピオネート]、2-エチルヘキシル-3-(3’,5’-ジ-tert-ブチル-4’-ヒドロキシフェニル)プロピオネート、2,2’-エチレンビス(4,6-ジ-tert-ブチルフェノール)、3,5-ジ-tert-ブチル-4-ヒドロキシベンゼンプロパン酸およびC13-15アルキルのエステル、2,5-ジ-tert-アミルヒドロキノン、ヒンダードフェノールの重合物(ADEKA POLYMER ADDITIVES EUROPE SAS社製 商品名「AO.OH.98」)、2,2’-メチレンビス[6-(1-メチルシクロヘキシル)-p-クレゾール]、2-tert-ブチル-6-(3-tert-ブチル-2-ヒドロキシ5-メチルベンジル)-4-メチルフェニルアクリレート、2-[1-(2-ヒドロキシ-3,5-ジ-tert-ペンチルフェニル)エチル]-4,6-ジ-tert-ペンチルフェニルアクリレート、6-[3-(3-tert-ブチル-4-ヒドロキシ-5-メチル)プロポキシ]-2,4,8,10-テトラ-tert-ブチルベンズ[d,f][1,3,2]-ジオキサホスフォビン、ヘキサメチレンビス[3-(3,5-ジ-tert-ブチル-4-ヒドロキシフェニル)プロピオネート]、ビス[モノエチル(3,5-ジ-tert-ブチル-4-ヒドロキシベンジル)ホスホネート]カルシウム塩、5,7-ビス(1,1-ジメチルエチル)-3-ヒドロキシ-2(3H)-ベンゾフラノンとo-キシレンとの反応生成物、2,6-ジ-tert-ブチル-4-(4,6-ビス(オクチルチオ)-1,3,5-トリアジン-2-イルアミノ)フェノール、DL-a-トコフェノール(ビタミンE)、2,6-ビス(α-メチルベンジル)-4-メチルフェノール、ビス[3,3-ビス-(4’-ヒドロキシ-3’-tert-ブチル-フェニル)ブタン酸]グリコールエステル、2,6-ジ-tert-ブチル-p-クレゾール、2,6-ジフェニル-4-オクタデシロキシフェノール、ステアリル(3,5-ジ-tert-ブチル-4-ヒドロキシフェニル)プロピオネート、ジステアリル(3,5-ジ-tert-ブチル-4-ヒドロキシベンジル)ホスホネート、トリデシル-3,5-tert-ブチル-4-ヒドロキシベンジルチオアセテート、チオジエチレンビス[(3,5-ジ-tert-ブチル-4-ヒドロキシフェニル)プロピオネート]、4,4’-チオビス(6-tert-ブチル-m-クレゾール)、2-オクチルチオ-4,6-ジ(3,5-ジ-tert-ブチル-4-ヒドロキシフェノキシ)-s-トリアジン、2,2’-メチレンビス(4-メチル-6-tert-ブチルフェノール)、ビス[3,3-ビス(4-ヒドロキシ-3-tert-ブチルフェニル)ブチリックアシッド]グリコールエステル、4,4’-ブチリデンビス(2,6-ジ-tert-ブチルフェノール)、4,4’-ブチリデンビス(6-tert-ブチル-3-メチルフェノール)、2,2’-エチリデンビス(4,6-ジ-tert-ブチルフェノール)、1,1,3-トリス(2-メチル-4-ヒドロキシ-5-tert-ブチルフェニル)ブタン、ビス[2-tert-ブチル-4-メチル-6-(2-ヒドロキシ-3-tert-ブチル-5-メチルベンジル)フェニル]テレフタレート、1,3,5-トリス(2,6-ジメチル-3-ヒドロキシ-4-tert-ブチルベンジル)イソシアヌレート、1,3,5-トリス(3,5-ジ-tert-ブチル-4-ヒドロキシベンジル)イソシアヌレート、1,3,5-トリス(3,5-ジ-tert-ブチル-4-ヒドロキシベンジル)-2,4,6-トリメチルベンゼン、1,3,5-トリス[(3,5-ジ-tert-ブチル-4-ヒドロキシフェニル)プロピオニルオキシエチル]イソシアヌレート、テトラキス[メチレン-3-(3’,5’-tert-ブチル-4’-ヒドロキシフェニル)プロピオネート]メタン、2-tert-ブチル-4-メチル-6-(2-アクリロイルオキシ-3-tert-ブチル-5-メチルベンジル)フェノール、3,9-ビス[2-(3-tert-ブチル-4-ヒドロキシ-5-メチルヒドロシンナモイルオキシ)-1,1-ジメチルエチル]-2,4,8,10-テトラオキサスピロ[5.5]ウンデカン、トリエチレングリコールビス[β-(3-tert-ブチル-4-ヒドロキシ-5-メチルフェニル)プロピオネート]、ステアリル-3-(3,5-ジ-tert-ブチル-4-ヒドロキシフェニル)プロピオン酸アミド、パルミチル-3-(3,5-ジ-tert-ブチル-4-ヒドロキシフェニル)プロピオン酸アミド、ミリスチル-3-(3,5-ジ-tert-ブチル-4-ヒドロキシフェニル)プロピオン酸アミド、ラウリル-3-(3,5-ジ-tert-ブチル-4-ヒドロキシフェニル)プロピオン酸アミド等の3-(3,5-ジアルキル-4-ヒドロキシフェニル)プロピオン酸誘導体等が挙げられる。 Examples of the phenolic antioxidant include 2,6-di-tert-butyl-4-ethylphenol, 2-tert-butyl-4,6-dimethylphenol, styrene phenol, and 2,2′-methylenebis (4). -Ethyl-6-tert-butylphenol), 2,2'-thiobis- (6-tert-butyl-4-methylphenol), 2,2'-thiodiethylenebis [3- (3,5-di-tert-) Butyl-4-hydroxyphenyl) propionate], 2-methyl-4,6-bis (octylsulfanylmethyl) phenol, 2,2'-isobutylidenebis (4,6-dimethylphenol), isooctyl-3- (3) , 5-Di-tert-butyl-4-hydroxyphenyl) propionate, N, N'-hexane-1,6-diylbis [3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionamide] , 2,2'-Oxamide-bis [ethyl-3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionate], 2-ethylhexyl-3- (3', 5'-di-tert- Butyl-4'-hydroxyphenyl) propionate, 2,2'-ethylenebis (4,6-di-tert-butylphenol), 3,5-di-tert-butyl-4-hydroxybenzenepropanoic acid and C13-15 alkyl , 2,5-Di-tert-amylhydroquinone, a polymer of hindered phenol (ADEKA POLYMER ADDITIVES EUROPE SAS, trade name "AO.OH.98"), 2,2'-methylenebis [6- (1) -Methylcyclohexyl) -p-cresol], 2-tert-butyl-6- (3-tert-butyl-2-hydroxy 5-methylbenzyl) -4-methylphenylacrylate, 2- [1- (2-hydroxy-) 3,5-Di-tert-pentylphenyl) ethyl] -4,6-di-tert-pentylphenyl acrylate, 6- [3- (3-tert-butyl-4-hydroxy-5-methyl) propoxy] -2 , 4,8,10-tetra-tert-butylbenz [d, f] [1,3,2] -dioxaphosphobin, hexamethylenebis [3- (3,5-di-tert-butyl-4-) Hydroxyphenyl) propionate], bis [monoethyl (3,5-di-tert-butyl-4-hydroxybenzyl) phosphonate] calcium salt, Reaction product of 5,7-bis (1,1-dimethylethyl) -3-hydroxy-2 (3H) -benzofuranone and o-xylene, 2,6-di-tert-butyl-4- (4,6) -Bis (octylthio) -1,3,5-triazine-2-ylamino) phenol, DL-a-tocophenol (vitamin E), 2,6-bis (α-methylbenzyl) -4-methylphenol, bis [ 3,3-Bis- (4'-hydroxy-3'-tert-butyl-phenyl) butanoic acid] glycol ester, 2,6-di-tert-butyl-p-cresol, 2,6-diphenyl-4-octa Decyloxyphenol, stearyl (3,5-di-tert-butyl-4-hydroxyphenyl) propionate, distearyl (3,5-di-tert-butyl-4-hydroxybenzyl) phosphonate, tridecyl-3,5-tert -Butyl-4-hydroxybenzylthioacetate, thiodiethylenebis [(3,5-di-tert-butyl-4-hydroxyphenyl) propionate], 4,4'-thiobis (6-tert-butyl-m-cresol) , 2-octylthio-4,6-di (3,5-di-tert-butyl-4-hydroxyphenoxy) -s-triazine, 2,2'-methylenebis (4-methyl-6-tert-butylphenol), bis [3,3-bis (4-hydroxy-3-tert-butylphenyl) butyric acid] glycol ester, 4,4'-butylidenebis (2,6-di-tert-butylphenol), 4,4'-butylidenebis ( 6-tert-butyl-3-methylphenol), 2,2'-ethylidenebis (4,6-di-tert-butylphenol), 1,1,3-tris (2-methyl-4-hydroxy-5-tert) -Butylphenyl) butane, bis [2-tert-butyl-4-methyl-6- (2-hydroxy-3-tert-butyl-5-methylbenzyl) phenyl] terephthalate, 1,3,5-tris (2, 6-Dimethyl-3-hydroxy-4-tert-butylbenzyl) isocyanurate, 1,3,5-tris (3,5-di-tert-butyl-4-hydroxybenzyl) isocyanurate, 1,3,5- Tris (3,5-di-tert-butyl-4-hydroxybenzyl) -2,4,6-trimethylbenzene, 1,3,5-tris [(3,5-di-tert-butyl-4-hydroxyphenyl) Nyl) propionyloxyethyl] isocyanurate, tetrakis [methylene-3- (3', 5'-tert-butyl-4'-hydroxyphenyl) propionate] methane, 2-tert-butyl-4-methyl-6- (2) -Acryloyloxy-3-tert-butyl-5-methylbenzyl) phenol, 3,9-bis [2- (3-tert-butyl-4-hydroxy-5-methylhydrocinnamoyloxy) -1,1-dimethyl Ethyl] -2,4,8,10-tetraoxaspiro [5.5] undecane, triethylene glycolbis [β- (3-tert-butyl-4-hydroxy-5-methylphenyl) propionate], stearyl-3 -(3,5-di-tert-butyl-4-hydroxyphenyl) propionic acid amide, palmityl-3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionic acid amide, myristyl-3- (3,5-di-tert-butyl-4-hydroxyphenyl) 3- (3,5) such as 3,5-di-tert-butyl-4-hydroxyphenyl) propionic acid amide, lauryl-3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionic acid amide, etc. -Dialkyl-4-hydroxyphenyl) propionic acid derivatives and the like can be mentioned.
 リン系酸化防止剤としては、例えば、トリフェニルホスファイト、ジイソオクチルホスファイト、ヘプタキス(ジプロピレングリコール)トリホスファイト、トリイソデシルホスファイト、ジフェニルイソオクチルホスファイト、ジイソオクチルフェニルホスファイト、ジフェニルトリデシルホスファイト、トリイソオクチルホスファイト、トリラウリルホスファイト、ジフェニルホスファイト、トリス(ジプロピレングリコール)ホスファイト、ジオレイルヒドロゲンホスファイト、トリラウリルトリチオホスファイト、ビス(トリデシル)ホスファイト、トリス(イソデシル)ホスファイト、トリス(トリデシル)ホスファイト、ジフェニルデシルホスファイト、ジノニルフェニルビス(ノニルフェニル)ホスファイト、ポリ(ジプロピレングリコール)フェニルホスファイト、テトラフェニルジプロピレングリコールジホスファイト、トリスノニルフェニルホスファイト、トリス(2,4-ジ-tert-ブチルフェニル)ホスファイト、トリス(2,4-ジ-tert-ブチル-5-メチルフェニル)ホスファイト、トリス〔2-tert-ブチル-4-(3-tert-ブチル-4-ヒドロキシ-5-メチルフェニルチオ)-5-メチルフェニル〕ホスファイト、トリ(デシル)ホスファイト、オクチルジフェニルホスファイト、ジ(デシル)モノフェニルホスファイト、ジステアリルペンタエリスリトールとステアリン酸カルシウム塩との混合物、アルキル(C10)ビスフェノールAホスファイト、テトラフェニル-テトラ(トリデシル)ペンタエリスリトールテトラホスファイト、ビス(2,4-ジ-tert-ブチル-6-メチルフェニル)エチルホスファイト、テトラ(トリデシル)イソプロピリデンジフェノールジホスファイト、テトラ(トリデシル)-4,4’-n-ブチリデンビス(2-tert-ブチル-5-メチルフェノール)ジホスファイト、ヘキサ(トリデシル)-1,1,3-トリス(2-メチル-4-ヒドロキシ-5-tert-ブチルフェニル)ブタントリホスファイト、テトラキス(2,4-ジ-tert-ブチルフェニル)ビフェニレンジホスホナイト、9,10-ジハイドロ-9-オキサ-10-ホスファフェナンスレン-10-オキサイド、(1-メチル-1-プロペニル-3-イリデン)トリス(1,1-ジメチルエチル)-5-メチル-4,1-フェニレン)ヘキサトリデシルホスファイト、2,2’-メチレンビス(4,6-ジ-tert-ブチルフェニル)-2-エチルヘキシルホスファイト、2,2’-メチレンビス(4,6-ジ-tert-ブチルフェニル)-オクタデシルホスファイト、2,2’-エチリデンビス(4,6-ジ-tert-ブチルフェニル)フルオロホスファイト、4,4’-ブチリデンビス(3-メチル-6-tert-ブチルフェニルジトリデシル)ホスファイト、トリス(2-〔(2,4,8,10-テトラキス-tert-ブチルジベンゾ〔d,f〕〔1,3,2〕ジオキサホスフェピン-6-イル)オキシ〕エチル)アミン、3,9-ビス(4-ノニルフェノキシ)-2,4,8,10-テトラオキサ-3,9-ジホスフェススピロ[5,5]ウンデカン、2,4,6-トリ-tert-ブチルフェニル-2-ブチル-2-エチル-1,3-プロパンジオールホスファイト、ポリ4,4’-イソプロピリデンジフェノールC12-15アルコールホスファイト、ビス(ジイソデシル)ペンタエリスリトールジホスファイト、ビス(トリデシル)ペンタエリスリトールジホスファイト、ビス(オクタデシル)ペンタエリスリトールジホスファイト、ビス(ノニルフェニル)ペンタエリスリトールジホスファイト、ビス(2,4-ジ-tert-ブチルフェニル)ペンタエリスリトールジホスファイト、ビス(2,4,6-トリ-tert-ブチルフェニル)ペンタエリスリトールジホスファイト、ビス(2,6-ジ-tert-ブチル-4-メチルフェニル)ペンタエリスリトールジホスファイト、ビス(2,4-ジクミルフェニル)ペンタエリスリトールジホスファイト等が挙げられる。 Examples of phosphorus-based antioxidants include triphenylphosphite, diisooctylphosphite, heptaxis (dipropylene glycol) triphosphite, triisodecylphosphite, diphenylisooctylphosphite, diisooctylphenylphosphite, and diphenyl. Tridecylphosphite, triisooctylphosphite, trilaurylphosphite, diphenylphosphite, tris (dipropylene glycol) phosphite, dioleylhydrogenphosphite, trilauryltrithiophosphite, bis (tridecyl) phosphite, tris (Isodecyl) phosphite, tris (tridecyl) phosphite, diphenyldecylphosphite, dinonylphenylbis (nonylphenyl) phosphite, poly (dipropylene glycol) phenylphosphite, tetraphenyldipropylene glycol diphosphite, trisnonyl Phenyl Phenyl Phenyl Phenyl, Tris (2,4-di-tert-Butylphenyl) Phenyl Phenyl, Tris (2,4-Di-tert-Butyl-5-Methylphenyl) Phenyl Phenyl, Tris [2-tert-Butyl-4- (3-tert-Butyl-4-hydroxy-5-Methylphenylthio) -5-Methylphenyl] Phenylphosphite, tri (decyl) phosphite, octyldiphenylphosphite, di (decyl) monophenylphosphenyl, distearylpenta Mixture of erythritol and calcium stearate, alkyl (C10) bisphenol A phosphite, tetraphenyl-tetra (tridecyl) pentaerythritol tetraphosphite, bis (2,4-di-tert-butyl-6-methylphenyl) ethylphos Fight, tetra (tridecyl) isopropyridene diphenol diphosphite, tetra (tridecyl) -4,4'-n-butylidenebis (2-tert-butyl-5-methylphenol) diphosphite, hexa (tridecyl) -1,1, 3-Tris (2-methyl-4-hydroxy-5-tert-butylphenyl) butanetriphosphite, tetrakis (2,4-di-tert-butylphenyl) biphenylenediphosphonite, 9,10-dihydro-9-oxa -10-Phenylphenylanthrene-10-oxide, (1-methyl-1-propenyl-3-ylidene) tris (1,1-dimethylethyl) -5-methyl-4,1-phenylene) hex Satridecylphosphite, 2,2'-methylenebis (4,6-di-tert-butylphenyl) -2-ethylhexylphosphite, 2,2'-methylenebis (4,6-di-tert-butylphenyl) -octadecyl Phosphite, 2,2'-ethylidenebis (4,6-di-tert-butylphenyl) fluorophosphite, 4,4'-butylidenebis (3-methyl-6-tert-butylphenylditridecyl) phosphite, tris (2-[(2,4,8,10-tetrakiss-tert-butyldibenzo [d, f] [1,3,2] dioxaphosfepine-6-yl) oxy] ethyl) amine, 3,9 -Bis (4-nonylphenoxy) -2,4,8,10-tetraoxa-3,9-diphosphespiro [5,5] undecane, 2,4,6-tri-tert-butylphenyl-2-butyl -2-Ethyl-1,3-propanediol phosphite, poly 4,4'-isopropyridene diphenol C12-15 alcohol phosphite, bis (diisodecyl) pentaerythritol diphosphite, bis (tridecyl) pentaerythritol diphosphite , Bis (octadecyl) pentaerythritol diphosphite, bis (nonylphenyl) pentaerythritol diphosphite, bis (2,4-di-tert-butylphenyl) pentaerythritol diphosphite, bis (2,4,6-tri) -Tert-Butylphenyl) pentaerythritol diphosphite, bis (2,6-di-tert-butyl-4-methylphenyl) pentaerythritol diphosphite, bis (2,4-dicumylphenyl) pentaerythritol diphosphite And so on.
 硫黄系酸化防止剤としては、例えば、テトラキス[メチレン-3-(ラウリルチオ)プロピオネート]メタン、ビス(メチル-4-[3-n-アルキル(C12/C14)チオプロピオニルオキシ]5-tert-ブチルフェニル)スルファイド、ジトリデシル-3,3’-チオジプロピオネート、ジラウリル-3,3’-チオジプロピオネート、ジミリスチル-3,3’-チオジプロピオネート、ジステアリル-3,3’-チオジプロピオネート、ラウリル/ステアリルチオジプロピオネート、4,4’-チオビス(6-tert-ブチル-m-クレゾール)、2,2’-チオビス(6-tert-ブチル-p-クレゾール)、ジステアリル-ジサルファイドが挙げられる。 Examples of the sulfur-based antioxidant include tetrakis [methylene-3- (laurylthio) propionate] methane and bis (methyl-4- [3-n-alkyl (C12 / C14) thiopropionyloxy] 5-tert-butylphenyl. ) Sulfide, ditridecyl-3,3'-thiodipropionate, dilauryl-3,3'-thiodipropionate, dimyristyl-3,3'-thiodipropionate, distearyl-3,3'-thiodipropio Nate, lauryl / stearylthiodipropionate, 4,4'-thiobis (6-tert-butyl-m-cresol), 2,2'-thiobis (6-tert-butyl-p-cresol), distearyl-di Sulfuride can be mentioned.
 その他の酸化防止剤としては、N-ベンジル-α-フェニルニトロン、N-エチル-α-メチルニトロン、N-オクチル-α-ヘプチルニトロン、N-ラウリル-α-ウンデシルニトロン、N-テトラデシル-α-トリデシルニトロン、N-ヘキサデシル-α-ペンタデシルニトロン、N-オクチル-α-ヘプタデシルニトロン、N-ヘキサデシル-α-ヘプタデシルニトロン、N-オクタデシル-α-ペンタデシルニトロン、N-ヘプタデシル-α-ヘプタデシルニトロン、N-オクタデシル-α-ヘプタデシルニトロン等のニトロン化合物、3-アリールベンゾフラン-2(3H)-オン、3-(アルコキシフェニル)ベンゾフラン-2-オン、3-(アシルオキシフェニル)ベンゾフラン-2(3H)-オン、5,7-ジ-tert-ブチル-3-(3,4-ジメチルフェニル)-ベンゾフラン-2(3H)-オン、5,7-ジ-tert-ブチル-3-(4-ヒドロキシフェニル)-ベンゾフラン-2(3H)-オン、5,7-ジ-tert-ブチル-3-{4-(2-ヒドロキシエトキシ)フェニル}-ベンゾフラン-2(3H)-オン、6-(2-(4-(5,7-ジ-tert-2-オキソ-2,3-ジヒドロベンゾフラン-3-イル)フェノキシ)エトキシ)-6-オキソヘキシル-6-((6-ヒドロキシヘキサノイル)オキシ)ヘキサノエート、5-ジ-tert-ブチル-3-(4-((15-ヒドロキシ-3,6,9,13-テトラオキサペンタデシル)オキシ)フェニル)ベンゾフラン-2(3H)オン等のベンゾフラン化合物等が挙げられる。 Other antioxidants include N-benzyl-α-phenylnitrone, N-ethyl-α-methylnitrone, N-octyl-α-heptylnitrone, N-lauryl-α-undecylnitrone, N-tetradecyl-α. -Tridecyl nitrone, N-hexadecyl-α-pentadecyl nitrone, N-octyl-α-heptadecyl nitrone, N-hexadecyl-α-heptadecylnitrone, N-octadecyl-α-pentadecylnitrone, N-heptadecyl-α -Nitron compounds such as heptadecylnitron, N-octadecyl-α-heptadecylnitron, 3-arylbenzofuran-2 (3H) -one, 3- (alkoxyphenyl) benzofuran-2-one, 3- (acyloxyphenyl) benzofuran -2 (3H) -one, 5,7-di-tert-butyl-3- (3,4-dimethylphenyl) -benzofuran-2 (3H) -one, 5,7-di-tert-butyl-3- (4-Hydroxyphenyl) -benzofuran-2 (3H) -one, 5,7-di-tert-butyl-3-{4- (2-hydroxyethoxy) phenyl} -benzofuran-2 (3H) -one, 6 -(2- (4- (5,7-di-tert-2-oxo-2,3-dihydrobenzofuran-3-yl) phenoxy) ethoxy) -6-oxohexyl-6-((6-hydroxyhexanoyl) ) Oxy) hexanoate, 5-di-tert-butyl-3-(4-((15-hydroxy-3,6,9,13-tetraoxapentadecyl) oxy) phenyl) benzofuran-2 (3H) on, etc. Examples include benzofuran compounds.
 ヒンダードアミン化合物としては、例えば、2,2,6,6-テトラメチル-4-ピペリジルステアレート、1,2,2,6,6-ペンタメチル-4-ピペリジルステアレート、2,2,6,6-テトラメチル-4-ピペリジルベンゾエート、ビス(2,2,6,6-テトラメチル-4-ピペリジル)セバケート、テトラキス(2,2,6,6-テトラメチル-4-ピペリジル)-1,2,3,4-ブタンテトラカルボキシレート、テトラキス(1,2,2,6,6-ペンタメチル-4-ピペリジル)-1,2,3,4-ブタンテトラカルボキシレート、ビス(2,2,6,6-テトラメチル-4-ピペリジル)・ジ(トリデシル)-1,2,3,4-ブタンテトラカルボキシレート、ビス(1,2,2,6,6-ペンタメチル-4-ピペリジル)-ジ(トリデシル)-1,2,3,4-ブタンテトラカルボキシレート、ビス(1,2,2,4,4-ペンタメチル-4-ピペリジル)-2-ブチル-2-(3,5-ジ-tert-ブチル-4-ヒドロキシベンジル)マロネート、1-(2-ヒドロキシエチル)-2,2,6,6-テトラメチル-4-ピペリジノ-ル/コハク酸ジエチル重縮合物、1,6-ビス(2,2,6,6-テトラメチル-4-ピペリジルアミノ)ヘキサン/2,4-ジクロロ-6-モルホリノ-s-トリアジン重縮合物、1,6-ビス(2,2,6,6-テトラメチル-4-ピペリジルアミノ)ヘキサン/2,4-ジクロロ-6-tert-オクチルアミノ-s-トリアジン重縮合物、1,5,8,12-テトラキス〔2,4-ビス(N-ブチル-N-(2,2,6,6-テトラメチル-4-ピペリジル)アミノ)-s-トリアジン-6-イル〕-1,5,8,12-テトラアザドデカン、1,5,8,12-テトラキス〔2,4-ビス(N-ブチル-N-(1,2,2,6,6-ペンタメチル-4-ピペリジル)アミノ)-s-トリアジン-6-イル〕-1,5,8-12-テトラアザドデカン、1,6,11-トリス[2,4-ビス(N-ブチル-N-(2,2,6,6-テトラメチル-4-ピペリジル)アミノ-s-トリアジン-6-イルアミノ]ウンデカン、1,6,11-トリス[2,4-ビス(N-ブチル-N-(1,2,2,6,6-ペンタメチル-4-ピペリジル)アミノ-s-トリアジン-6-イルアミノ]ウンデカン、3,9-ビス〔1,1-ジメチル-2-{トリス(2,2,6,6-テトラメチル-4-ピペリジルオキシカルボニル)ブチルカルボニルオキシ}エチル〕-2,4,8,10-テトラオキサスピロ〔5.5〕ウンデカン、3,9-ビス〔1,1-ジメチル-2-{トリス(1,2,2,6,6-ペンタメチル-4-ピペリジルオキシカルボニル)ブチルカルボニルオキシ}エチル〕-2,4,8,10-テトラオキサスピロ〔5.5〕ウンデカン、ビス(1-ウンデシルオキシ-2,2,6,6-テトラメチルピペリジン-4-イル)カーボネート、2,2,6,6-テトラメチル-4-ピペリジルヘキサデカノエート、2,2,6,6-テトラメチル-4-ピペリジルオクタデカノエート等が挙げられる。 Examples of the hindered amine compound include 2,2,6,6-tetramethyl-4-piperidyl stearate, 1,2,2,6,6-pentamethyl-4-piperidyl stearate, 2,2,6,6- Tetramethyl-4-piperidylbenzoate, bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate, tetrakis (2,2,6,6-tetramethyl-4-piperidyl) -1,2,3 , 4-Butan Tetracarboxylate, Tetrakiss (1,2,2,6,6-Pentamethyl-4-piperidyl) -1,2,3,4-Butane Tetracarboxylate, Bis (2,2,6,6- Tetramethyl-4-piperidyl) di (tridecyl) -1,2,3,4-butanetetracarboxylate, bis (1,2,2,6,6-pentamethyl-4-piperidyl) -di (tridecyl)- 1,2,3,4-butanetetracarboxylate, bis (1,2,2,4,4-pentamethyl-4-piperidyl) -2-butyl-2- (3,5-di-tert-butyl-4) -Hydroxybenzyl) malonate, 1- (2-hydroxyethyl) -2,2,6,6-tetramethyl-4-piperidinol / diethyl polycondensate succinate, 1,6-bis (2,2,6) , 6-Tetramethyl-4-piperidylamino) hexane / 2,4-dichloro-6-morpholino-s-triazine polycondensate, 1,6-bis (2,2,6,6-tetramethyl-4-piperidyl) Amino) hexane / 2,4-dichloro-6-tert-octylamino-s-triazine polycondensate, 1,5,8,12-tetrakis [2,4-bis (N-butyl-N- (2,2)) , 6,6-Tetramethyl-4-piperidyl) amino) -s-triazine-6-yl] -1,5,8,12-tetraazadodecane, 1,5,8,12-tetrakis [2,4- Bis (N-butyl-N- (1,2,2,6,6-pentamethyl-4-piperidyl) amino) -s-triazine-6-yl] -1,5,8-12-tetraazadodecane, 1, , 6,11-Tris [2,4-bis (N-butyl-N- (2,2,6,6-tetramethyl-4-piperidyl) amino-s-triazine-6-ylamino] undecane, 1,6 , 11-Tris [2,4-bis (N-butyl-N- (1,2,2,6,6-pentamethyl-4-piperidyl) amino-s-triazine-6-ylamino] undecane, 3,9- Bis [1,1-dimethyl-2- {Tris (2, 2,6,6-tetramethyl-4-piperidyloxycarbonyl) butylcarbonyloxy} ethyl] -2,4,8,10-tetraoxaspiro [5.5] undecane, 3,9-bis [1,1- Dimethyl-2- {tris (1,2,2,6,6-pentamethyl-4-piperidyloxycarbonyl) butylcarbonyloxy} ethyl] -2,4,8,10-tetraoxaspiro [5.5] undecane, Bis (1-undecyloxy-2,2,6,6-tetramethylpiperidine-4-yl) carbonate, 2,2,6,6-tetramethyl-4-piperidylhexadecanoate, 2,2,6 , 6-Tetramethyl-4-piperidyl octadecanoate and the like.
 紫外線吸収剤としては、例えば、2,4-ジヒドロキシベンゾフェノン、5,5’-メチレンビス(2-ヒドロキシ-4-メトキシベンゾフェノン)等の2-ヒドロキシベンゾフェノン類;2-(2-ヒドロキシ-5-メチルフェニル)ベンゾトリアゾール、2-(2-ヒドロキシ-5-tert-オクチルフェニル)ベンゾトリアゾール、2-(2-ヒドロキシ-3,5-ジ-tert-ブチルフェニル)-5-クロロベンゾトリアゾール、2-(2-ヒドロキシ-3-tert-ブチル-5-メチルフェニル)-5-クロロベンゾトリアゾール、2-(2-ヒドロキシ-3,5-ジクミルフェニル)ベンゾトリアゾール、2,2’-メチレンビス(4-tert-オクチル-6-ベンゾトリアゾリルフェノール)、2-(2-ヒドロキシ-3-tert-ブチル-5-カルボキシフェニル)ベンゾトリアゾールのポリエチレングリコールエステル、2-〔2-ヒドロキシ-3-(2-アクリロイルオキシエチル)-5-メチルフェニル〕ベンゾトリアゾール、2-〔2-ヒドロキシ-3-(2-メタクリロイルオキシエチル)-5-tert-ブチルフェニル〕ベンゾトリアゾール、2-〔2-ヒドロキシ-3-(2-メタクリロイルオキシエチル)-5-tert-オクチルフェニル〕ベンゾトリアゾール、2-〔2-ヒドロキシ-3-(2-メタクリロイルオキシエチル)-5-tert-ブチルフェニル〕-5-クロロベンゾトリアゾール、2-〔2-ヒドロキシ-5-(2-メタクリロイルオキシエチル)フェニル〕ベンゾトリアゾール、2-〔2-ヒドロキシ-3-tert-ブチル-5-(2-メタクリロイルオキシエチル)フェニル〕ベンゾトリアゾール、2-〔2-ヒドロキシ-3-tert-アミル-5-(2-メタクリロイルオキシエチル)フェニル〕ベンゾトリアゾール、2-〔2-ヒドロキシ-3-tert-ブチル-5-(3-メタクリロイルオキシプロピル)フェニル〕-5-クロロベンゾトリアゾール、2-〔2-ヒドロキシ-4-(2-メタクリロイルオキシメチル)フェニル〕ベンゾトリアゾール、2-〔2-ヒドロキシ-4-(3-メタクリロイルオキシ-2-ヒドロキシプロピル)フェニル〕ベンゾトリアゾール、2-〔2-ヒドロキシ-4-(3-メタクリロイルオキシプロピル)フェニル〕ベンゾトリアゾール等の2-(2-ヒドロキシフェニル)ベンゾトリアゾール類;フェニルサリシレート、レゾルシノールモノベンゾエート、2,4-ジ-tert-ブチルフェニル-3,5-ジ-tert-ブチル-4-ヒドロキシベンゾエート、オクチル(3,5-ジ-tert-ブチル-4-ヒドロキシ)ベンゾエート、ドデシル(3,5-ジ-tert-ブチル-4-ヒドロキシ)ベンゾエート、テトラデシル(3,5-ジ-tert-ブチル-4-ヒドロキシ)ベンゾエート、ヘキサデシル(3,5-ジ-tert-ブチル-4-ヒドロキシ)ベンゾエート、オクタデシル(3,5-ジ-tert-ブチル-4-ヒドロキシ)ベンゾエート、ベヘニル(3,5-ジ-tert-ブチル-4-ヒドロキシ)ベンゾエート等のベンゾエート類;2-エチル-2’-エトキシオキザニリド、2-エトキシ-4’-ドデシルオキザニリド等の置換オキザニリド類;エチル-α-シアノ-β,β-ジフェニルアクリレート、メチル-2-シアノ-3-メチル-3-(p-メトキシフェニル)アクリレート等のシアノアクリレート類;2-(4,6-ジフェニル-1,3,5-トリアジン-2-イル)-5-ヘキシルオキシフェノール、2-(2-ヒドロキシ-4-オクトキシフェニル)-4,6-ビス(2,4-ジメチルフェニル)-1,3,5-トリアジン、トリオクチル-2,2’,2”-((1,3,5-トリアジン-2,4,6-トリイル)トリス(3-ヒドロキシベンゼン-4-,1-ジイル)トリプロピオネート)、2-(4,6-ジフェニル-1,3,5-トリアジン-2-イル)-5-[2-(2-エチルヘキサノイルオキシ)エトキシ]フェノール、2,4,6-トリス(2-ヒドロキシ-4-ヘキシルオキシ-3-メチルフェニル)-1,3,5-トリアジン、1,12-ビス[2-[4-(4,6-ジフェニル-1,3,5-トリアジン-2-イル)-3-ヒドロキシフェノキシ]エチル]ドデカンジオエート等のトリアジン類;各種の金属塩、または金属キレート、特にニッケル、クロムの塩、またはキレート類等が挙げられる。 Examples of the ultraviolet absorber include 2-hydroxybenzophenones such as 2,4-dihydroxybenzophenone and 5,5'-methylenebis (2-hydroxy-4-methoxybenzophenone); 2- (2-hydroxy-5-methylphenyl). ) Bentriazole, 2- (2-hydroxy-5-tert-octylphenyl) benzotriazole, 2- (2-hydroxy-3,5-di-tert-butylphenyl) -5-chlorobenzotriazole, 2- (2) -Hydroxy-3-tert-butyl-5-methylphenyl) -5-chlorobenzotriazole, 2- (2-hydroxy-3,5-dicumylphenyl) benzotriazole, 2,2'-methylenebis (4-tert- Octyl-6-benzotriazolylphenol), 2- (2-hydroxy-3-tert-butyl-5-carboxyphenyl) benzotriazole polyethylene glycol ester, 2- [2-hydroxy-3- (2-acryloyloxy) Ethyl) -5-methylphenyl] benzotriazole, 2- [2-hydroxy-3- (2-methacryloyloxyethyl) -5-tert-butylphenyl] benzotriazole, 2- [2-hydroxy-3- (2-) Methacryloyloxyethyl) -5-tert-octylphenyl] benzotriazole, 2- [2-hydroxy-3- (2-methacryloyloxyethyl) -5-tert-butylphenyl] -5-chlorobenzotriazole, 2- [2 -Hydroxy-5- (2-methacryloyloxyethyl) phenyl] benzotriazole, 2- [2-hydroxy-3-tert-butyl-5- (2-methacryloyloxyethyl) phenyl] benzotriazole, 2- [2-hydroxy -3-tert-Amil-5- (2-methacryloyloxyethyl) phenyl] benzotriazole, 2- [2-hydroxy-3-tert-butyl-5- (3-methacryloyloxypropyl) phenyl] -5-chlorobenzo Triazole, 2- [2-hydroxy-4- (2-methacryloyloxymethyl) phenyl] benzotriazole, 2- [2-hydroxy-4- (3-methacryloyloxy-2-hydroxypropyl) phenyl] benzotriazole, 2- [2-Hydroxy-4- (3-methacryloyloxypropyl) phenyl] 2- (2-Hydroxyphenyl) benzotriazoles such as benzotriazole Phenylsalicylate, resorcinol monobenzoate, 2,4-di-tert-butylphenyl-3,5-di-tert-butyl-4-hydroxybenzoate, octyl (3,5-di-tert-butyl-4-hydroxy) Benzoate, dodecyl (3,5-di-tert-butyl-4-hydroxy) benzoate, tetradecyl (3,5-di-tert-butyl-4-hydroxy) benzoate, hexadecyl (3,5-di-tert-butyl- Benzoates such as 4-hydroxy) benzoate, octadecyl (3,5-di-tert-butyl-4-hydroxy) benzoate, behenyl (3,5-di-tert-butyl-4-hydroxy) benzoate; 2-ethyl- Substituted oxanilides such as 2'-ethoxyoxanilide, 2-ethoxy-4'-dodecyloxanilide; ethyl-α-cyano-β, β-diphenylacrylate, methyl-2-cyano-3-methyl-3- Cyanoacrylates such as (p-methoxyphenyl) acrylate; 2- (4,6-diphenyl-1,3,5-triazine-2-yl) -5-hexyloxyphenol, 2- (2-hydroxy-4-) Octoxyphenyl) -4,6-bis (2,4-dimethylphenyl) -1,3,5-triazine, trioctyl-2,2', 2 "-((1,3,5-triazine-2,4) , 6-Triyl) Tris (3-hydroxybenzene-4-,1-diyl) tripropionate), 2- (4,6-diphenyl-1,3,5-triazine-2-yl) -5-[2 -(2-Ethylhexanoyloxy) ethoxy] phenol, 2,4,6-tris (2-hydroxy-4-hexyloxy-3-methylphenyl) -1,3,5-triazine, 1,12-bis [ Triazines such as 2- [4- (4,6-diphenyl-1,3,5-triazine-2-yl) -3-hydroxyphenoxy] ethyl] dodecandioate; various metal salts or metal chelates, especially Examples thereof include nickel, chromium salts, and chelates.
 難燃剤としては、例えば、トリフェニルホスフェート、トリクレジルホスフェート、トリキシレニルホスフェート、クレジルジフェニルホスフェート、クレジル-2,6-ジキシレニルホスフェート、レゾルシノールビス(ジフェニルホスフェート)、(1-メチルエチリデン)-4,1-フェニレンテトラフェニルジホスフェート、1,3-フェニレンテトラキス(2,6-ジメチルフェニル)ホスフェート、株式会社ADEKA製商品名「アデカスタブFP-500」、「アデカスタブFP-600」、「アデカスタブFP-800」の芳香族リン酸エステル、フェニルホスホン酸ジビニル、フェニルホスホン酸ジアリル、フェニルホスホン酸(1-ブテニル)等のホスホン酸エステル、ジフェニルホスフィン酸フェニル、ジフェニルホスフィン酸メチル、9,10-ジヒドロ-9-オキサ-10-ホスファフェナントレン-10-オキシド誘導体等のホスフィン酸エステル、ビス(2-アリルフェノキシ)ホスファゼン、ジクレジルホスファゼン等のホスファゼン化合物、リン酸メラミン、ピロリン酸メラミン、ポリリン酸メラミン、ポリリン酸メラム、ポリリン酸アンモニウム、リン酸ピペラジン、ピロリン酸ピペラジン、ポリリン酸ピペラジン、リン含有ビニルベンジル化合物および赤リン等のリン系難燃剤、水酸化マグネシウム、水酸化アルミニウム等の金属水酸化物、臭素化ビスフェノールA型エポキシ樹脂、臭素化フェノールノボラック型エポキシ樹脂、ヘキサブロモベンゼン、ペンタブロモトルエン、エチレンビス(ペンタブロモフェニル)、エチレンビステトラブロモフタルイミド、1,2-ジブロモ-4-(1,2-ジブロモエチル)シクロヘキサン、テトラブロモシクロオクタン、ヘキサブロモシクロドデカン、ビス(トリブロモフェノキシ)エタン、臭素化ポリフェニレンエーテル、臭素化ポリスチレンおよび2,4,6-トリス(トリブロモフェノキシ)-1,3,5-トリアジン、トリブロモフェニルマレイミド、トリブロモフェニルアクリレート、トリブロモフェニルメタクリレート、テトラブロモビスフェノールA型ジメタクリレート、ペンタブロモベンジルアクリレート、および、臭素化スチレン等の臭素系難燃剤等が挙げられる。これら難燃剤はフッ素樹脂等のドリップ防止剤や多価アルコール、ハイドロタルサイト等の難燃助剤と併用することが好ましい。 Examples of the flame retardant include triphenyl phosphate, tricresyl phosphate, trixylenyl phosphate, cresyldiphenyl phosphate, cresyl-2,6-dixylenyl phosphate, resorcinolbis (diphenyl phosphate), (1-methylethylidene). -4,1-Phenylenetetraphenyldiphosphate, 1,3-phenylenetetrakis (2,6-dimethylphenyl) phosphate, manufactured by ADEKA Co., Ltd. Product names "Adecastab FP-500", "Adecastab FP-600", "Adecastab FP" -800 "aromatic phosphate ester, divinyl phenylphosphonate, diallyl phenylphosphonate, phosphonic acid ester such as phenylphosphonic acid (1-butenyl), phenyl diphenylphosphinate, methyl diphenylphosphinate, 9,10-dihydro- Phenylate esters such as 9-oxa-10-phosphaphenanthrene-10-oxide derivative, phosphazene compounds such as bis (2-allylphenoxy) phosphazene, dicredylphosphazene, melamine phosphate, melamine pyrophosphate, melamine polyphosphate, polyline Phenyl-based flame retardants such as melam acid, ammonium polyphosphate, piperazine phosphate, piperazine pyrophosphate, piperazine polyphosphate, phosphorus-containing vinylbenzyl compound and red phosphorus, metal hydroxides such as magnesium hydroxide and aluminum hydroxide, bromide. Bisphenol A type epoxy resin, brominated phenol novolac type epoxy resin, hexabromobenzene, pentabromotoluene, ethylenebis (pentabromophenyl), ethylenebistetrabromophthalimide, 1,2-dibromo-4- (1,2-dibromo) Ethyl) cyclohexane, tetrabromocyclooctane, hexabromocyclododecane, bis (tribromophenoxy) ethane, brominated polyphenylene ether, brominated polystyrene and 2,4,6-tris (tribromophenoxy) -1,3,5- Examples thereof include triazine, tribromophenylmaleimide, tribromophenyl acrylate, tribromophenyl methacrylate, tetrabromobisphenol A type dimethacrylate, pentabromobenzyl acrylate, and bromine-based flame retardants such as brominated styrene. These flame retardants are preferably used in combination with a drip inhibitor such as fluororesin and a flame retardant aid such as polyhydric alcohol and hydrotalcite.
 滑剤としては、例えば、オレイン酸アミド、エルカ酸アミド等の不飽和脂肪酸アミド;ベヘン酸アミド、ステアリン酸アミド等の飽和脂肪酸アミド、ブチルステアレート、ステアリルアルコール、ステアリン酸モノグリセライド、ソルビタンモノパルミチテート、ソルビタンモノステアレート、マンニトール、ステアリン酸、硬化ひまし油、ステアリンサンアマイド、オレイン酸アマイド、エチレンビスステアリン酸アマイド等が挙げられる。 Examples of the lubricant include unsaturated fatty acid amides such as oleic acid amide and erucic acid amide; saturated fatty acid amides such as bechenic acid amide and stearic acid amide, butyl stearate, stearyl alcohol, stearic acid monoglyceride, and sorbitan monopalmitite. Examples thereof include sorbitan monostearate, mannitol, stearic acid, hardened castor oil, stearic acid amide, oleic acid amide, and ethylene bisstearic acid amide.
 充填剤としては、例えばタルク、マイカ、炭酸カルシウム、酸化カルシウム、水酸化カルシウム、炭酸マグネシウム、水酸化マグネシウム、酸化マグネシウム、硫酸マグネシウム、水酸化アルミニウム、硫酸バリウム、ガラス粉末、ガラス繊維、クレー、ドロマイト、シリカ、アルミナ、チタン酸カリウムウィスカー、ワラステナイト、繊維状マグネシウムオキシサルフェート等を挙げることができ、粒子径(繊維状においては繊維径や繊維長およびアスペクト比)を適宜選択して用いることができる。これら充填剤の中では、剛性を付与する効果に優れ、かつ入手が容易であることから、タルクが特に好ましく用いられる。また、充填剤は、必要に応じて表面処理したものを用いることができる。 As fillers, for example, talc, mica, calcium carbonate, calcium oxide, calcium hydroxide, magnesium carbonate, magnesium hydroxide, magnesium oxide, magnesium sulfate, aluminum hydroxide, barium sulfate, glass powder, glass fiber, clay, dolomite, etc. Examples thereof include silica, alumina, potassium titanate whiskers, wallastenite, and fibrous magnesium oxysulfate, and the particle size (fiber diameter, fiber length, and aspect ratio in the fibrous form) can be appropriately selected and used. Among these fillers, talc is particularly preferably used because it has an excellent effect of imparting rigidity and is easily available. Further, as the filler, a surface-treated filler can be used if necessary.
 脂肪酸金属塩としては、例えば直鎖または分岐状の脂肪酸残基を含む炭素原子数12~20の脂肪酸の金属塩等が挙げられる。脂肪酸金属塩を構成する金属イオンとしては、例えばナトリウムイオン、カリウムイオン、リチウムイオン、ジヒドロキシアルミニウムイオン、カルシウムイオン、亜鉛イオン、バリウムイオン、マグネシウムイオン、ヒドロキシアルミニウムイオン等が挙げられ、これらの中でもナトリウムイオン、カリウムイオン、リチウムイオンが特に好ましい。 Examples of the fatty acid metal salt include a metal salt of a fatty acid having 12 to 20 carbon atoms including a linear or branched fatty acid residue. Examples of the metal ion constituting the fatty acid metal salt include sodium ion, potassium ion, lithium ion, dihydroxyaluminum ion, calcium ion, zinc ion, barium ion, magnesium ion, hydroxyaluminum ion and the like, and among these, sodium ion. , Potassium ion, lithium ion are particularly preferable.
 ハイドロタルサイト類は、天然物や合成物として知られるマグネシウム、アルミニウム、水酸基、炭酸基および任意の結晶水からなる複合塩化合物であり、マグネシウムまたはアルミニウムの一部をアルカリ金属や亜鉛等他の金属で置換したものや水酸基、炭酸基を他のアニオン基で置換したものが挙げられる。ハイドロタルサイト類は、結晶水を脱水したものであってもよく、ステアリン酸等の高級脂肪酸、オレイン酸アルカリ金属塩等の高級脂肪酸金属塩、ドデシルベンゼンスルホン酸アルカリ金属塩等の有機スルホン酸金属塩、高級脂肪酸アミド、高級脂肪酸エステルまたはワックス等で被覆されたものであってもよい。ハイドロタルサイト類は、天然物であってもよく、また合成品であってもよい。ハイドロタルサイト類の合成方法としては、特公昭46-2280号公報、特公昭50-30039号公報、特公昭51-29129号公報、特公平3-36839号公報、特開昭61-174270号公報、特開平5-179052号公報等に記載されている公知の方法が挙げられる。また、ハイドロタルサイト類は、その結晶構造、結晶粒子等に制限されることなく使用することができる。 Hydrotalcites are complex salt compounds consisting of magnesium, aluminum, hydroxyl groups, carbonic acid groups and arbitrary crystalline water known as natural products and synthetic products, and magnesium or aluminum is partly made of other metals such as alkali metals and zinc. Examples thereof include those substituted with, and those substituted with a hydroxyl group and a carbonic acid group with another anionic group. Hydrotalcites may be obtained by dehydrating crystalline water, and are higher fatty acids such as stearic acid, higher fatty acid metal salts such as oleic acid alkali metal salt, and organic sulfonic acid metals such as dodecylbenzene sulfonic acid alkali metal salt. It may be coated with a salt, a higher fatty acid amide, a higher fatty acid ester, a wax or the like. The hydrotalcites may be natural products or synthetic products. Examples of the method for synthesizing hydrotalcites include Japanese Patent Publication No. 46-2280, Japanese Patent Publication No. 50-30039, Japanese Patent Publication No. 51-29129, Japanese Square Root Extraction 3-36839, and Japanese Patent Application Laid-Open No. 61-174270. , Known methods described in JP-A-5-179502, etc. can be mentioned. Further, hydrotalcites can be used without being limited by their crystal structure, crystal particles and the like.
 帯電防止剤としては、例えば、非イオン性、アニオン性、カチオン性または両性の界面活性剤等による低分子型帯電防止剤、高分子化合物による高分子型帯電防止型が挙げられる。非イオン性界面活性剤としては、高級アルコールエチレンオキシド付加物、脂肪酸エチレンオキシド付加物、高級アルキルアミンエチレンオキシド付加物、ポリオレフィングリコールエチレンオキシド付加物等のポリエチレングリコール型非イオン界面活性剤;ポリエチレンオキシド、グリセリンの脂肪酸エステル、ペンタエリスリットの脂肪酸エステル、ソルビット若しくはソルビタンの脂肪酸エステル、多価アルコールのアルキルエーテル、アルカノールアミンの脂肪族アミド等の多価アルコール型非イオン界面活性剤等が挙げられ、アニオン性界面活性剤としては、例えば、高級脂肪酸のアルカリ金属塩等のカルボン酸塩;高級アルコール硫酸エステル塩、高級アルキルエーテル硫酸エステル塩等の硫酸エステル塩、アルキルベンゼンスルホン酸塩、アルキルスルホン酸塩、パラフィンスルホン酸塩等のスルホン酸塩;高級アルコールリン酸エステル塩等のリン酸エステル塩等が挙げられ、カチオン性界面活性剤としては、アルキルトリメチルアンモニウム塩等の第4級アンモニウム塩等が挙げられる。両性界面活性剤としては、高級アルキルアミノプロピオン酸塩等のアミノ酸型両性界面活性剤、高級アルキルジメチルベタイン、高級アルキルジヒドロキシエチルベタイン等のベタイン型両性界面活性剤等が挙げられる。これらの中ではアニオン性界面活性剤が好ましく、特に、アルキルベンゼンスルホン酸塩、アルキルスルホン酸塩、パラフィンスルホン酸塩等のスルホン酸塩が好ましい。 Examples of the antistatic agent include a low molecular weight antistatic agent using a nonionic, anionic, cationic or amphoteric surfactant, and a polymer type antistatic agent using a polymer compound. Nonionic surfactants include polyethylene glycol-type nonionic surfactants such as higher alcohol ethylene oxide adducts, fatty acid ethylene oxide adducts, higher alkylamine ethylene oxide adducts, and polyolefin glycol ethylene oxide adducts; fatty acid esters of polyethylene oxide and glycerin. , Pentaerislit fatty acid ester, sorbit or sorbitan fatty acid ester, polyhydric alcohol alkyl ether, polyhydric alcohol type nonionic surfactant such as aliphatic amide of alkanolamine, etc., and examples thereof include anionic surfactants. Is, for example, a carboxylate such as an alkali metal salt of a higher fatty acid; a sulfate ester salt such as a higher alcohol sulfate ester salt, a higher alkyl ether sulfate ester salt, an alkylbenzene sulfonate, an alkyl sulfonate, a paraffin sulfonate and the like. Sulfates: Phosphoric acid ester salts such as higher alcohol phosphoric acid ester salts and the like can be mentioned, and examples of the cationic surfactant include quaternary ammonium salts such as alkyltrimethylammonium salt and the like. Examples of the amphoteric tenside include amino acid amphoteric tenside agents such as higher alkylaminopropionate, betaine amphoteric tenside agents such as higher alkyldimethylbetaine and higher alkyldihydroxyethyl betaine, and the like. Among these, anionic surfactants are preferable, and sulfonates such as alkylbenzene sulfonates, alkyl sulfonates, and paraffin sulfonates are particularly preferable.
 高分子型帯電防止剤としては、アイオノマーやポリエチレングリコールを親水部とするブロックポリマー等が挙げられる。アイオノマーとしては特開2010-132927号公報に記載のアイオノマーが挙げられる。ポリエチレングリコールを親水部とするポリマーとしては、例えば特開平7-10989号公報に記載のポリエーテルエステルアミド、米国特許第6552131号公報記載のポリオレフィンとポリエチレングリコールからなるポリマー、特開2016-023254号公報記載のポリエステルとポリエチレングリコールからなるポリマー等が挙げられる。 Examples of the polymer type antistatic agent include ionomer and block polymer having polyethylene glycol as a hydrophilic part. Examples of the ionomer include the ionomer described in JP-A-2010-132927. Examples of the polymer having polyethylene glycol as a hydrophilic portion include a polyether ester amide described in JP-A-7-10989, a polymer composed of polyolefin and polyethylene glycol described in US Pat. No. 6,552,131, and JP-A-2016-023254. Examples thereof include the above-mentioned polymers composed of polyester and polyethylene glycol.
 蛍光増白剤とは、太陽光や人工光の紫外線を吸収し、これを紫~青色の可視光線に変えて輻射する蛍光作用によって、成形体の白色度や青味を助長させる化合物である。蛍光増白剤としては、ベンゾオキサゾール系化合物C.I.Fluorescent Brightener184;クマリン系化合物C.I.Fluorescent Brightener52;ジアミノスチルベンジスルフォン酸系化合物C.I.Fluorescent Brightener24、85、71等が挙げられる。 Fluorescent whitening agent is a compound that absorbs ultraviolet rays of sunlight or artificial light, converts it into visible light of purple to blue and radiates it, and promotes the whiteness and bluish tint of the molded product. Examples of the fluorescent whitening agent include benzoxazole compounds C.I. I. Fluorescent Fluorescent 184; Coumarin-based compound C.I. I. Fluorescent Fluorescent 52; diaminostilbene disulphonic acid-based compound C.I. I. Fluorescent Fluorescenter 24, 85, 71 and the like can be mentioned.
 顔料は特に限定されるものではなく、市販の顔料を用いることもできる。顔料の具体例としては、例えばピグメントレッド1、2、3、9、10、17、22、23、31、38、41、48、49、88、90、97、112、119、122、123、144、149、166、168、169、170、171、177、179、180、184、185、192、200、202、209、215、216、217、220、223、224、226、227、228、240、254;ピグメントオレンジ13、31、34、36、38、43、46、48、49、51、52、55、59、60、61、62、64、65、71;ピグメントイエロー1、3、12、13、14、16、17、20、24、55、60、73、81、83、86、93、95、97、98、100、109、110、113、114、117、120、125、126、127、129、137、138、139、147、148、150、151、152、153、154、166、168、175、180、185;ピグメントグリーン7、10、36;ピグメントブルー15、15:1、15:2、15:3、15:4、15:5、15:6、22、24、29、56、60、61、62、64;ピグメントバイオレット1、15、19、23、27、29、30、32、37、40、50等が挙げられる。 The pigment is not particularly limited, and a commercially available pigment can also be used. Specific examples of pigments include, for example, Pigment Red 1, 2, 3, 9, 10, 17, 22, 23, 31, 38, 41, 48, 49, 88, 90, 97, 112, 119, 122, 123, 144, 149, 166, 168, 169, 170, 171, 177, 179, 180, 184, 185, 192, 200, 202, 209, 215, 216, 217, 220, 223, 224, 226, 227, 228, 240, 254; Pigment Orange 13, 31, 34, 36, 38, 43, 46, 48, 49, 51, 52, 55, 59, 60, 61, 62, 64, 65, 71; Pigment Yellow 1, 3, 12, 13, 14, 16, 17, 20, 24, 55, 60, 73, 81, 83, 86, 93, 95, 97, 98, 100, 109, 110, 113, 114, 117, 120, 125, 126, 127, 129, 137, 138, 139, 147, 148, 150, 151, 152, 153, 154, 166, 168, 175, 180, 185; Pigment Green 7, 10, 36; Pigment Blue 15, 15: 1, 15: 2, 15: 3, 15: 4, 15: 5, 15: 6, 22, 24, 29, 56, 60, 61, 62, 64; Pigment Violet 1, 15, 19, 23, 27, 29, 30, 32, 37, 40, 50 and the like can be mentioned.
 染料としては、例えばアゾ染料、アントラキノン染料、インジゴイド染料、トリアリールメタン染料、キサンテン染料、アリザリン染料、アクリジン染料、スチルベン染料、チアゾール染料、ナフトール染料、キノリン染料、ニトロ染料、インダミン染料、オキサジン染料、フタロシアニン染料、シアニン染料等の染料が挙げられる。 Examples of dyes include azo dyes, anthraquinone dyes, indigoid dyes, triarylmethane dyes, xanthene dyes, alizarin dyes, acrydin dyes, stillben dyes, thiazole dyes, naphthol dyes, quinoline dyes, nitro dyes, indamine dyes, oxazine dyes, and phthalocyanine. Dyes such as dyes and cyanine dyes can be mentioned.
 本実施形態の透明化剤は、さらにポリオレフィン系樹脂を含むマスターバッチであってもよい。 The clearing agent of the present embodiment may be a master batch further containing a polyolefin resin.
 マスターバッチに含まれるポリオレフィン系樹脂としては、例えば、低密度ポリエチレン、直鎖状低密度ポリエチレン、高密度ポリエチレン、架橋ポリエチレン、超高分子量ポリエチレンなどのポリエチレン系樹脂、ホモポリプロピレン、ランダムコポリマーポリプロピレン、ブロックコポリマーポリプロピレン、インパクトコポリマーポリプロピレン、ハイインパクトコポリマーポリプロピレン、無水マレイン酸変性ポリプロピレンなどのポリプロピレン系樹脂、ポリブテン-1、シクロオレフィンポリマー、ポリ-3-メチル-1-ブテン、ポリ-3-メチル-1-ペンテン、ポリ-4-メチル-1-ペンテン等のα-オレフィン重合体、エチレン-メチルメタクリレート共重合体、エチレン-酢酸ビニル共重合体等のα-オレフィン共重合体等が挙げられる。これらポリオレフィン系樹脂は、1種が単独で用いられても、2種以上が併用されてもよい。またポリオレフィン系樹脂はアロイ化されていてもよい。ポリオレフィン系樹脂の分子量、重合度、密度、軟化点、溶媒への不溶分の割合、立体規則性の程度、触媒残渣の有無、原料となるモノマーの種類や配合比率、重合に使用される触媒の種類(例えば、チーグラー触媒、メタロセン触媒等)等は特に限定されるものではなく、適宜選択される。 Examples of the polyolefin-based resin contained in the master batch include polyethylene-based resins such as low-density polyethylene, linear low-density polyethylene, high-density polyethylene, crosslinked polyethylene, and ultrahigh-molecular-weight polyethylene, homopolypoly, random copolymer polypropylene, and block copolymer. Polypropylene resins such as polypropylene, impact copolymer polypropylene, high impact copolymer polypropylene, maleic anhydride-modified polypropylene, polybutene-1, cycloolefin polymer, poly-3-methyl-1-butene, poly-3-methyl-1-pentene, Examples thereof include α-olefin polymers such as poly-4-methyl-1-pentene, ethylene-methylmethacrylate copolymers, and α-olefin copolymers such as ethylene-vinyl acetate copolymers. One of these polyolefin resins may be used alone, or two or more thereof may be used in combination. Further, the polyolefin resin may be alloyed. Molecular weight, degree of polymerization, density, softening point, ratio of insoluble matter in solvent, degree of stereoregularity, presence or absence of catalyst residue, type and compounding ratio of raw material monomer, catalyst used for polymerization The type (for example, Cheegler catalyst, metallocene catalyst, etc.) is not particularly limited and is appropriately selected.
 マスターバッチに含まれるポリオレフィン系樹脂としては、ポリプロピレン系樹脂が特に好ましい。 As the polyolefin resin contained in the masterbatch, a polypropylene resin is particularly preferable.
 透明化剤がポリオレフィン系樹脂を含むマスターバッチである場合、マスターバッチ中におけるポリオレフィン系樹脂の含有量は、例えば90質量%以下であればよく、80質量%以下であることが好ましく、60質量%以下であることがより好ましい。また、マスターバッチ中におけるポリオレフィン系樹脂の含有量は、例えば20質量%以上であればよい。 When the clearing agent is a master batch containing a polyolefin resin, the content of the polyolefin resin in the master batch may be, for example, 90% by mass or less, preferably 80% by mass or less, and 60% by mass. The following is more preferable. The content of the polyolefin resin in the masterbatch may be, for example, 20% by mass or more.
 さらに、本実施形態の透明化剤は、バインダー、ワックス、溶剤、シリカ等の造粒助剤がさらに配合され、造粒されたワンパック複合添加剤であってもよい。 Further, the clearing agent of the present embodiment may be a one-pack composite additive further blended with a granulating aid such as a binder, wax, solvent, and silica, and granulated.
 次に、本発明の実施形態に係る樹脂組成物について説明する。
<樹脂組成物>
 本実施形態の樹脂組成物は、ポリオレフィン系樹脂と、上記(A)一般式(1)で表されるトリアジン化合物と、上記(B)一般式(2)で表されるアセタール化合物とを含む。そして、(A)トリアジン化合物の含有量(質量部)と(B)アセタール化合物の含有量(質量部)との比(A)/(B)が1/99~99/1であり、ポリオレフィン系樹脂100質量部に対する(A)トリアジン化合物および(B)アセタール化合物の合計含有量が0.001~10質量部である。
Next, the resin composition according to the embodiment of the present invention will be described.
<Resin composition>
The resin composition of the present embodiment contains a polyolefin-based resin, a triazine compound represented by the above (A) general formula (1), and an acetal compound represented by the above (B) general formula (2). The ratio (A) / (B) of the content (parts by mass) of the (A) triazine compound to the content (parts by mass) of the (B) acetal compound is 1/99 to 99/1, and is polyolefin-based. The total content of the (A) triazine compound and the (B) acetal compound with respect to 100 parts by mass of the resin is 0.001 to 10 parts by mass.
 本実施形態の樹脂組成物によれば、優れた透明性を備える成形品が得られる。 According to the resin composition of the present embodiment, a molded product having excellent transparency can be obtained.
 本実施形態の樹脂組成物に含まれるポリオレフィン系樹脂としては、上述のマスターバッチに含まれるポリオレフィン系樹脂と同じものが挙げられる。樹脂組成物に含まれるポリオレフィン系樹脂は、ポリプロピレン系樹脂であることが好ましい。この場合、優れた耐熱性を備える成形品を得ることができる。 Examples of the polyolefin-based resin contained in the resin composition of the present embodiment include the same polyolefin-based resins contained in the above-mentioned masterbatch. The polyolefin-based resin contained in the resin composition is preferably a polypropylene-based resin. In this case, a molded product having excellent heat resistance can be obtained.
 上述したように、本実施形態の樹脂組成物において、(A)トリアジン化合物の含有量(質量部)と(B)アセタール化合物の含有量(質量部)との比(A)/(B)は1/99~99/1である。より優れた透明性を備える成形品を得る観点から、(A)/(B)の値は10/90以上であることが好ましく、25/75以上であることがより好ましい。また、同様の観点から、(A)/(B)の値は90/10以下であることが好ましく、75/25以下であることがより好ましい。 As described above, in the resin composition of the present embodiment, the ratio (A) / (B) of the content (parts by mass) of the (A) triazine compound to the content (parts by mass) of the (B) acetal compound is It is 1/99 to 99/1. From the viewpoint of obtaining a molded product having more excellent transparency, the value of (A) / (B) is preferably 10/90 or more, and more preferably 25/75 or more. From the same viewpoint, the value of (A) / (B) is preferably 90/10 or less, and more preferably 75/25 or less.
 また、上述したように、本実施形態の樹脂組成物において、ポリオレフィン系樹脂100質量部に対する(A)トリアジン化合物および(B)アセタール化合物の合計含有量は、0.001~10質量部である。(A)トリアジン化合物および(B)アセタール化合物の合計含有量が0.001質量部未満である場合、成形品の透明性が十分に優れたものとならない。また、(A)トリアジン化合物および(B)アセタール化合物の合計含有量が10質量部を超える場合も成形品の透明性が十分に優れたものとならず、さらに成形品の表面にブルームが発生する場合や、(A)トリアジン化合物または(B)アセタール化合物が成形品から他の物品に移行する場合がある。成形品の透明性をさらに優れたものとする観点から、ポリオレフィン系樹脂100質量部に対する(A)トリアジン化合物および(B)アセタール化合物の合計含有量は0.01質量部以上であることが好ましく、0.02質量部以上であることがより好ましく、0.05質量部以上であることがさらに好ましい。また、成形品の透明性をさらに優れたものとし、かつブルームの発生や(A)トリアジン化合物および(B)アセタール化合物の移行を十分に抑制する観点から、ポリオレフィン系樹脂100質量部に対する(A)トリアジン化合物および(B)アセタール化合物の合計含有量は2質量部以下であることが好ましく、1質量部以下であることがより好ましく、0.5質量部以下であることがさらに好ましく、0.3質量部以下であることがさらに一層好ましく、0.1質量部以下であることが特に好ましい。 Further, as described above, in the resin composition of the present embodiment, the total content of the (A) triazine compound and the (B) acetal compound is 0.001 to 10 parts by mass with respect to 100 parts by mass of the polyolefin resin. When the total content of the (A) triazine compound and the (B) acetal compound is less than 0.001 part by mass, the transparency of the molded product is not sufficiently excellent. Further, when the total content of the (A) triazine compound and the (B) acetal compound exceeds 10 parts by mass, the transparency of the molded product is not sufficiently excellent, and bloom is generated on the surface of the molded product. In some cases, the (A) triazine compound or (B) acetal compound may be transferred from the molded product to another article. From the viewpoint of further improving the transparency of the molded product, the total content of the (A) triazine compound and (B) acetal compound with respect to 100 parts by mass of the polyolefin resin is preferably 0.01 part by mass or more. It is more preferably 0.02 parts by mass or more, and further preferably 0.05 parts by mass or more. Further, from the viewpoint of further improving the transparency of the molded product and sufficiently suppressing the generation of bloom and the transfer of (A) triazine compound and (B) acetal compound, (A) with respect to 100 parts by mass of the polyolefin-based resin. The total content of the triazine compound and the (B) acetal compound is preferably 2 parts by mass or less, more preferably 1 part by mass or less, further preferably 0.5 parts by mass or less, and 0.3. It is even more preferably parts by mass or less, and particularly preferably 0.1 parts by mass or less.
 ポリオレフィン系樹脂100質量部に対する(A)トリアジン化合物の含有量は、例えば0.0005~9.9995質量部であればよく、0.01~5質量部であることが好ましく、0.01~2質量部であることがより好ましく、0.02~1質量部であることがさらに好ましく、0.05~0.5質量部であることがさらに一層好ましく、0.05~0.3質量部であることが特に好ましい。また、ポリオレフィン系樹脂100質量部に対する(B)アセタール化合物の含有量は、例えば0.0005~9.9995質量部であればよく、0.01~5質量部であることが好ましく、0.01~2質量部であることがより好ましく、0.02~1質量部であることがさらに好ましく、0.05~0.5質量部であることがさらに一層好ましく、0.05~0.3質量部であることが特に好ましい。 The content of the (A) triazine compound with respect to 100 parts by mass of the polyolefin resin may be, for example, 0.0005 to 9.9995 parts by mass, preferably 0.01 to 5 parts by mass, and 0.01 to 2 parts by mass. It is more preferably parts by mass, more preferably 0.02 to 1 part by mass, further preferably 0.05 to 0.5 parts by mass, and 0.05 to 0.3 parts by mass. It is particularly preferable to have. The content of the (B) acetal compound with respect to 100 parts by mass of the polyolefin resin may be, for example, 0.0005 to 9.9995 parts by mass, preferably 0.01 to 5 parts by mass, and 0.01. It is more preferably to 2 parts by mass, further preferably 0.02 to 1 part by mass, further preferably 0.05 to 0.5 parts by mass, and 0.05 to 0.3 parts by mass. It is particularly preferable that it is a part.
 本実施形態の樹脂組成物には、(A)トリアジン化合物および(B)アセタール化合物以外に、フェノール系酸化防止剤、リン系酸化防止剤、硫黄系酸化防止剤、その他の酸化防止剤、ヒンダードアミン化合物、紫外線吸収剤、難燃剤、難燃助剤、滑剤、充填剤、ハイドロタルサイト類、脂肪酸金属塩、帯電防止剤、蛍光増白剤、顔料および染料等の各種添加剤が含まれていてもよい。これら各種添加剤としては、上述の透明化剤に含まれてもよい添加剤として例示したものと同じものが挙げられる。 In addition to the (A) triazine compound and (B) acetal compound, the resin composition of the present embodiment includes a phenol-based antioxidant, a phosphorus-based antioxidant, a sulfur-based antioxidant, other antioxidants, and a hindered amine compound. , UV absorbers, flame retardants, flame retardants, lubricants, fillers, hydrotalcites, fatty acid metal salts, antioxidants, fluorescent whitening agents, pigments and dyes, etc. good. Examples of these various additives include the same as those exemplified as the additives that may be contained in the above-mentioned clearing agent.
 次に、本発明の実施形態に係る樹脂組成物の製造方法について説明する。
<樹脂組成物の製造方法>
 本実施形態の樹脂組成物の製造方法は、ポリオレフィン系樹脂に、上記(A)一般式(1)で表されるトリアジン化合物と、上記(B)一般式(2)で表されるアセタール化合物と、を配合する工程を含む。そして、(A)トリアジン化合物の配合量(質量部)と(B)アセタール化合物の配合量(質量部)との比(A)/(B)が1/99~99/1であり、ポリオレフィン系樹脂100質量部に対する(A)トリアジン化合物および(B)アセタール化合物の合計配合量が0.001~10質量部である。
Next, a method for producing the resin composition according to the embodiment of the present invention will be described.
<Manufacturing method of resin composition>
In the method for producing a resin composition of the present embodiment, a polyolefin resin is mixed with a triazine compound represented by the above (A) general formula (1) and an acetal compound represented by the above (B) general formula (2). , Including the step of blending. The ratio (A) / (B) of the compounding amount (parts by mass) of the (A) triazine compound and the compounding amount (parts by mass) of the (B) acetal compound is 1/99 to 99/1, and is a polyolefin-based compound. The total amount of the (A) triazine compound and the (B) acetal compound to be blended with respect to 100 parts by mass of the resin is 0.001 to 10 parts by mass.
 本実施形態の樹脂組成物の製造方法で製造された樹脂組成物からなる成形品は、優れた透明性を有するものになる。 The molded product made of the resin composition produced by the method for producing the resin composition of the present embodiment has excellent transparency.
 ポリオレフィン系樹脂に(A)トリアジン化合物および(B)アセタール化合物を配合する方法としては特に限定されるものではなく、例えばポリオレフィン系樹脂に(A)トリアジン化合物、(B)アセタール化合物および必要に応じて上述の各種添加剤を配合した後、ヘンシェルミキサー、ミルロール、バンバリーミキサー、スーパーミキサー等の混合装置を用いて混合する方法などが挙げられる。ここで、(A)トリアジン化合物、(B)アセタール化合物および上述の各種添加剤は、上述した透明化剤の形態で、ポリオレフィン系樹脂に配合されてもよい。また、(A)トリアジン化合物、(B)アセタール化合物および上述の各種添加剤のうち少なくとも一つの成分が、ポリオレフィン系樹脂モノマーまたはオリゴマーの重合前または重合中に配合され、得られた重合体に残りの成分が配合されてもよい。さらに、樹脂組成物の製造方法は、上述の方法によって得られた混合物をさらに単軸押出機、二軸押出機等の溶融混練装置を用いて溶融混練する工程を含む方法であってもよい。ここで溶融混練の温度は、例えば180~280℃であればよい。 The method for blending the (A) triazine compound and the (B) acetal compound with the polyolefin resin is not particularly limited, and for example, the (A) triazine compound, the (B) acetal compound and, if necessary, the polyolefin resin. Examples thereof include a method of blending the above-mentioned various additives and then mixing them using a mixing device such as a Henschel mixer, a mill roll, a Banbury mixer, or a super mixer. Here, the (A) triazine compound, (B) acetal compound and the above-mentioned various additives may be blended with the polyolefin-based resin in the form of the above-mentioned clearing agent. Further, at least one component of (A) triazine compound, (B) acetal compound and the above-mentioned various additives is blended before or during polymerization of the polyolefin resin monomer or oligomer, and remains in the obtained polymer. Ingredients may be blended. Further, the method for producing the resin composition may be a method including a step of further melt-kneading the mixture obtained by the above-mentioned method using a melt-kneading device such as a single-screw extruder or a twin-screw extruder. Here, the temperature of melt-kneading may be, for example, 180 to 280 ° C.
 本発明の樹脂組成物の製造方法は、上記実施形態に限定されるものではなく、その他の製造方法として、例えば、ポリオレフィン系樹脂と上記(A)一般式(1)で表されるトリアジン化合物とを含む樹脂組成物に、上記(B)一般式(2)で表されるアセタール化合物を配合する工程を含む製造方法、ポリオレフィン系樹脂と上記(B)一般式(2)で表されるアセタール化合物とを含む樹脂組成物に、上記(A)一般式(1)で表されるトリアジン化合物を配合する工程を含む製造方法等が挙げられる。 The method for producing the resin composition of the present invention is not limited to the above embodiment, and other production methods include, for example, a polyolefin resin and the triazine compound represented by the above general formula (A). A production method including the step of blending the acetal compound represented by the general formula (2) in the resin composition containing (B), the polyolefin resin and the acetal compound represented by the general formula (2) above. Examples thereof include a production method including a step of blending the triazine compound represented by the general formula (1) in the resin composition containing the above (A).
 上述したその他の製造方法は、ポリオレフィン系樹脂および上記(A)一般式(1)で表されるトリアジン化合物を含む樹脂組成物からなる成形品、または、ポリオレフィン系樹脂および上記(B)一般式(2)で表されるアセタール化合物を含む樹脂組成物からなる成形品の廃材を粉砕して得られる樹脂組成物を原料としてリサイクル材料を製造する際などに好適に用いることができる。 The above-mentioned other production method is a molded product composed of a polyolefin resin and a resin composition containing the triazine compound represented by the above (A) general formula (1), or a polyolefin resin and the above (B) general formula ( It can be suitably used when producing a recycled material using a resin composition obtained by crushing a waste material of a molded product made of a resin composition containing an acetal compound represented by 2) as a raw material.
 次に、本発明の実施形態に係る成形品について説明する。
<成形品>
 本実施形態の成形品は、上述した樹脂組成物を成形して得られるものである。この成形品は透明性が優れたものになる。
Next, the molded article according to the embodiment of the present invention will be described.
<Molded product>
The molded product of this embodiment is obtained by molding the above-mentioned resin composition. This molded product has excellent transparency.
 成形品としては、射出成形品、繊維、フラットヤーン、二軸延伸フィルム、一軸延伸フィルム、無延伸フィルム、シート、サーモフォーミング成形品、押出ブロー成形品、射出ブロー成形品、射出延伸ブロー成形品、異形押出成形品、回転成形品等の成形品が挙げられる。成形品の好ましい具体例としては、ボトル、ジャー、カップ、バケツ、箱、缶、タンク等の容器が挙げられる。成形品が容器である場合、優れた透明性を備えるという特徴を有効に活用できる。 Molded products include injection molded products, fibers, flat yarns, biaxially stretched films, uniaxially stretched films, non-stretched films, sheets, thermoforming molded products, extrusion blow molded products, injection blow molded products, injection stretch blow molded products, Examples thereof include molded products such as deformed extrusion molded products and rotary molded products. Preferred specific examples of the molded product include containers such as bottles, jars, cups, buckets, boxes, cans and tanks. When the molded product is a container, the feature of having excellent transparency can be effectively utilized.
 成形品を製造する方法としては、特に限定されるものではなく、例えば、射出成形法、押出成形法、ブロー成形法、回転成形、真空成形法、インフレーション成形法、カレンダー成形法、スラッシュ成形法、ディップ成形法、サーモフォーミング成形法等の方法が挙げられる。 The method for producing the molded product is not particularly limited, and for example, an injection molding method, an extrusion molding method, a blow molding method, a rotary molding, a vacuum molding method, an inflation molding method, a calendar molding method, a slash molding method, etc. Examples include a dip molding method and a thermoforming molding method.
 以下、本発明を、実施例を用いてさらに詳細に説明するが、本発明はこれらに限定されるものではない。 Hereinafter, the present invention will be described in more detail with reference to examples, but the present invention is not limited thereto.
 実施例において用いられたトリアジン化合物およびアセタール化合物は以下の通りである。
トリアジン化合物-1:化合物No.60
トリアジン化合物-2:化合物No.49
トリアジン化合物-3:化合物No.61
トリアジン化合物-4:化合物No.6
トリアジン化合物-5:化合物No.59
アセタール化合物-1:化合物No.63
アセタール化合物-2:化合物No.62
The triazine compounds and acetal compounds used in the examples are as follows.
Triazine Compound-1: Compound No. 60
Triazine Compound-2: Compound No. 49
Triazine Compound-3: Compound No. 61
Triazine Compound-4: Compound No. 6
Triazine Compound-5: Compound No. 59
Acetal Compound-1: Compound No. 63
Acetal Compound-2: Compound No. 62
<トリアジン化合物の調製>
(トリアジン化合物-1)
 蒸留水300mLに水酸化ナトリウム6.5g、4-フェニルフェノール20.4g、4-ヒドロキシベンズアミド2.06gを溶解した溶液を調整した。別のフラスコでシアヌル酸クロリド11.1gをアセトン300mLに溶解し、氷浴で5℃まで冷却した。調整した溶液をゆっくり滴下し、滴下後室温にて4時間撹拌した。生成した沈殿をろ別し、蒸留水で洗浄・乾燥した後、展開溶媒をアセトン/酢酸エチルとしたシリカゲルカラムクロマトグラフィーにより化合物NO.60を単離した。得られた白色固体を乳鉢で粉砕し、300μmのメッシュを通過させることにより粗大粒子を除去し、トリアジン化合物-1を得た。
<Preparation of triazine compound>
(Triazine compound-1)
A solution prepared by dissolving 6.5 g of sodium hydroxide, 20.4 g of 4-phenylphenol, and 2.06 g of 4-hydroxybenzamide in 300 mL of distilled water was prepared. 11.1 g of cyanuric chloride was dissolved in 300 mL of acetone in another flask and cooled to 5 ° C. in an ice bath. The prepared solution was slowly added dropwise, and after the addition, the mixture was stirred at room temperature for 4 hours. The generated precipitate was filtered off, washed with distilled water and dried, and then compound No. 1 was obtained by silica gel column chromatography using acetone / ethyl acetate as the developing solvent. 60 was isolated. The obtained white solid was pulverized in a mortar and passed through a mesh of 300 μm to remove coarse particles to obtain triazine compound-1.
(トリアジン化合物-2)
 原料として4-フェニルフェノール、4-シクロヘキシルフェノール、4-ヒドロキシベンズアミドおよびシアヌル酸クロリドを使用した以外は上記と同様の手順で、トリアジン化合物-2を調製した。
(Triazine compound-2)
Triazine compound-2 was prepared by the same procedure as above except that 4-phenylphenol, 4-cyclohexylphenol, 4-hydroxybenzamide and cyanuric chloride were used as raw materials.
(トリアジン化合物-3)
 原料として4-シクロヘキシルフェノールおよびシアヌル酸クロリドを使用した以外は上記と同様の手順で、トリアジン化合物-3を調製した。
(Triazine compound-3)
Triazine compound-3 was prepared by the same procedure as above except that 4-cyclohexylphenol and cyanuric chloride were used as raw materials.
(トリアジン化合物-4)
 原料としてp-クレゾール、4-ヒドロキシベンズアミドおよびシアヌル酸クロリドを使用した以外は上記と同様の手順で、トリアジン化合物-4を調製した。
(Triazine compound-4)
Triazine compound-4 was prepared by the same procedure as above except that p-cresol, 4-hydroxybenzamide and cyanuric chloride were used as raw materials.
(トリアジン化合物-5)
 原料として4-フェニルフェノール、4-n-プロピルフェノール、4-ヒドロキシベンズアミドおよびシアヌル酸クロリドを使用した以外は上記と同様の手順で、トリアジン化合物-5を調製した。
(Triazine compound-5)
Triazine compound-5 was prepared by the same procedure as above except that 4-phenylphenol, 4-n-propylphenol, 4-hydroxybenzamide and cyanuric chloride were used as raw materials.
<透明化剤の作製>
(実施例1~8および比較例1~2)
 表1、2に示す配合割合で(A)トリアジン化合物および(B)アセタール化合物を配合し、乳鉢を用いて粉砕混合することにより、実施例1~8および比較例1~2の透明化剤を作製した。
<Preparation of transparent agent>
(Examples 1 to 8 and Comparative Examples 1 to 2)
By blending the (A) triazine compound and the (B) acetal compound in the blending ratios shown in Tables 1 and 2 and pulverizing and mixing them using a mortar, the clearing agents of Examples 1 to 8 and Comparative Examples 1 and 2 were obtained. Made.
<透明性の評価>
 図1は、透明性の評価において作製される積層体の断面図であり、図2は、実施例の透明性の評価において透過率を測定する点を説明するための図であり、試料を上から見た図である。先ず、第一のカバーガラス1の上に、プロピレンランダム共重合体(荷重2.16kg、測定温度230℃におけるメルトフローレート12g/10min、プライムポリマー社製 商品名「プライムポリプロ R720」)からなる3mm×3mm×300μmの正方形フィルム2を配置した。次に、このフィルム2上の中央部に、上記の透明化剤3を約0.05mg配置した。さらに、透明化剤3の上に第二のカバーガラス4を配置し、積層体10を得た。こうして得られた積層体10を、第一のカバーガラス1からなる面を下にして、温度制御機能付きホットステージの上に設置した後、第二のカバーガラス4の上面に1gの重りを乗せることにより、積層体10を均一に押圧した。続いて、押圧された積層体10を、ホットステージのヒーターを用いて、室温から100℃/minの速度で220℃まで加熱し、220℃で3min保持した後、100℃/minで室温まで冷却した。こうして熱処理をした後の積層体を試料20とし、クロスニコルに配置した2枚の偏光板の間に試料20を配置した際の光透過率を測定することにより、実施例1~8および比較例1~2の透明化剤を含む樹脂組成物からなる成形品の透明性を評価した。具体的には、顕微紫外可視分光光度計(日本分光社製 MSV-5100)を用い、測定波長を500nm、INアパーチャーを30μm、OUTアパーチャーを100μmに設定し、光源から第一の偏光板(偏光子)、試料20および第二の偏光板を通過して検出器にて検出された光の強度Iを測定し、透過率T(%)を算出した。
<Evaluation of transparency>
FIG. 1 is a cross-sectional view of a laminate produced in the evaluation of transparency, and FIG. 2 is a diagram for explaining a point of measuring the transmittance in the evaluation of transparency of an example, and the sample is above. It is a figure seen from. First, 3 mm of a propylene random copolymer (load 2.16 kg, melt flow rate 12 g / 10 min at a measurement temperature of 230 ° C., product name "Prime Polypro R720" manufactured by Prime Polymer Co., Ltd.) on the first cover glass 1. A square film 2 having a size of × 3 mm × 300 μm was placed. Next, about 0.05 mg of the above-mentioned clearing agent 3 was placed in the central portion on the film 2. Further, the second cover glass 4 was placed on the clearing agent 3 to obtain a laminated body 10. The laminate 10 thus obtained is placed on a hot stage with a temperature control function with the surface formed of the first cover glass 1 facing down, and then a 1 g weight is placed on the upper surface of the second cover glass 4. As a result, the laminated body 10 was pressed uniformly. Subsequently, the pressed laminate 10 is heated from room temperature to 220 ° C. at a rate of 100 ° C./min using a heater of a hot stage, held at 220 ° C. for 3 min, and then cooled to room temperature at 100 ° C./min. bottom. The laminate after the heat treatment was used as the sample 20, and the light transmittance when the sample 20 was placed between the two polarizing plates placed on the cloth Nicol was measured to measure Examples 1 to 8 and Comparative Examples 1 to 1. The transparency of the molded product made of the resin composition containing the clearing agent of No. 2 was evaluated. Specifically, using a microultraviolet visible spectrophotometer (MSV-5100 manufactured by JASCO Corporation), the measurement wavelength was set to 500 nm, the IN aperture was set to 30 μm, and the OUT aperture was set to 100 μm, and the first polarizing plate (polarized light) was set from the light source. The intensity I of the light passed through the sample 20 and the second polarizing plate and detected by the detector was measured, and the transmittance T (%) was calculated.
 なお、透過率T(%)は以下のようにして算出した。すなわち、試料および第二の偏光板(検光子)を配置せず、第一の偏光板(偏光子)のみを配置して測定を行った際の光の強度をI100とし、試料および第二の偏光板(検光子)を配置せず、第一の偏光板(偏光子)を配置するとともに、第二の偏光板(検光子)の代わりに黒板を配置して測定を行った際の光の強度をIとして、下記式より透過率T(%)を算出した。
T(%)=100×(I-I)/(I100-I
The transmittance T (%) was calculated as follows. That is, the intensity of light when the measurement is performed by arranging only the first polarizing plate (polarizer) without arranging the sample and the second polarizing plate (photometer) is set to I 100 , and the sample and the second polarizing plate (photometer) are arranged. Light when the first polarizing plate (polarizer) is placed and the black plate is placed instead of the second polarizing plate (photometer) to perform the measurement without arranging the polarizing plate (photometer) of the above. The transmittance T (%) was calculated from the following formula, where I 0 was set to the intensity of.
T (%) = 100 x (I-I 0 ) / (I 100- I 0 )
 図2に示すように、試料20の中央部には、溶融固化して凝集した透明化剤の粒子5が存在する。この粒子の外縁の1点Aと粒子の中心点Oとを通る直線上、点Aから粒子の外側に向かって30μm間隔で30点の測定点X~X30を設定し、上記の条件にて透過率T(%)を測定した。ここで、測定点X~X30における透過率T(%)の測定値をそれぞれY~Y30とする。隣接する3個の測定点における透過率T(%)の測定値の平均m=(Y+Yi+1+Yi+2)/3(i=1~28)を算出し、算出されたm~m28のうち最も小さい値を、実施例1~8および比較例1~2の透明化剤を含む樹脂組成物からなる成形品の透明性の指標とし、表1~2に「透過率(%)」として示した。なお、透明化剤3を配置しない以外は上記と同様にして積層体を作製し、上記と同様に熱処理をした後、上記と同様の測定を行った際の透過率T(%)の値は、60~70%であった。 As shown in FIG. 2, in the central portion of the sample 20, particles 5 of the clearing agent that have been melt-solidified and aggregated are present. Straight line passing through the center point O of the point A and the particles of the outer edge of the particle, set the measurement points X 1 ~ X 30 30 points at 30μm intervals toward the point A on the outside of the particle, the above conditions The transmittance T (%) was measured. Here, the measured value of the transmittance T (%) at the measurement point X 1 ~ X 30 and Y 1 ~ Y 30, respectively. The average mi = (Y i + Y i + 1 + Y i + 2 ) / 3 (i = 1 to 28) of the measured values of the transmittance T (%) at the three adjacent measurement points was calculated, and the calculated m 1 to m. The smallest value among 28 is used as an index of the transparency of the molded product composed of the resin composition containing the clearing agents of Examples 1 to 8 and Comparative Examples 1 and 2, and "Transmittance (%)) is shown in Tables 1 and 2. It was shown as. The value of the transmittance T (%) when the laminate was prepared in the same manner as above except that the transparent agent 3 was not arranged, the heat treatment was performed in the same manner as above, and then the same measurement as above was performed. , 60-70%.
 上記のようにして得られた透過率の測定値が透明化剤を含む樹脂組成物からなる成形品の透明性の指標となる理由は以下の通りである。すなわち、上記測定において、第一の偏光板(偏光子)によって偏光された光源からの光が試料に入射し、入射光が試料中でポリオレフィン系樹脂の粗大結晶によって散乱される場合、散乱光の偏光面は回転するため、散乱光は第二の偏光板(検光子)を通過して、検出器により検出される。一方、入射光が試料中で散乱されない場合、入射光は検光子により遮断されるため、検出器により検出されない。したがって、上記測定における透過率の測定値が小さいほど、全入射光に対する、散乱光の割合が小さいといえる。したがって、上記測定における透過率の測定値が小さいほど、透明化剤を含む樹脂組成物からなる成形品は、より優れた透明性を有するものであるといえる。 The reason why the measured value of the transmittance obtained as described above serves as an index of the transparency of the molded product made of the resin composition containing the transparent agent is as follows. That is, in the above measurement, when the light from the light source polarized by the first polarizing plate (polarizer) is incident on the sample and the incident light is scattered by the coarse crystals of the polyolefin resin in the sample, the scattered light Since the plane of polarization rotates, the scattered light passes through the second polarizing plate (photometer) and is detected by the detector. On the other hand, when the incident light is not scattered in the sample, the incident light is blocked by the detector and is not detected by the detector. Therefore, it can be said that the smaller the measured value of the transmittance in the above measurement, the smaller the ratio of the scattered light to the total incident light. Therefore, it can be said that the smaller the measured value of the transmittance in the above measurement, the more excellent the transparency of the molded product made of the resin composition containing the transparent agent.
Figure JPOXMLDOC01-appb-T000035
Figure JPOXMLDOC01-appb-T000035
Figure JPOXMLDOC01-appb-T000036
Figure JPOXMLDOC01-appb-T000036
 表1、2に示す結果から、実施例1~8の透明化剤は、成形品に優れた透明性を付与できるものであることが分かった。一方、比較例1~2の透明化剤は、成形品に十分な透明性を付与できるものとはいえなかった。 From the results shown in Tables 1 and 2, it was found that the clearing agents of Examples 1 to 8 can impart excellent transparency to the molded product. On the other hand, the clearing agents of Comparative Examples 1 and 2 could not be said to be able to impart sufficient transparency to the molded product.
 以上より、本発明の透明化剤は、成形品に優れた透明性を付与できるものであることが確認された。 From the above, it was confirmed that the transparent agent of the present invention can impart excellent transparency to the molded product.

Claims (10)

  1.  (A)下記一般式(1)、
    Figure JPOXMLDOC01-appb-I000001
    (一般式(1)中、Ar、ArおよびArは、それぞれ独立に、無置換のフェニル基または置換基を有するフェニル基を表す。)で表されるトリアジン化合物と、
     (B)下記一般式(2)、
    Figure JPOXMLDOC01-appb-I000002
    (一般式(2)中、Rは水素原子または炭素原子数1~4のアルキル基を表す。R、R、RおよびRはそれぞれ独立に水素原子、ハロゲン原子、シアノ基、炭素原子数1~4のアルキル基または炭素原子数1~4のアルコキシ基を表し、あるいはRおよびRまたはRおよびRが互いに連結して炭素原子数3~6のアルキレン基または炭素原子数1~4のアルキレンジオキシ基を表す。Xは単結合、-CH(OH)-基または-CH(OH)CH(OH)-基を表す。)で表されるアセタール化合物と、
    を含み、
     前記(A)トリアジン化合物の含有量(質量部)と前記(B)アセタール化合物の含有量(質量部)との比(A)/(B)が1/99~99/1であることを特徴とする透明化剤。
    (A) The following general formula (1),
    Figure JPOXMLDOC01-appb-I000001
    (In the general formula (1), Ar 1 , Ar 2 and Ar 3 each independently represent an unsubstituted phenyl group or a phenyl group having a substituent.)
    (B) The following general formula (2),
    Figure JPOXMLDOC01-appb-I000002
    (In the general formula (2), R 1 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. R 2 , R 3 , R 4 and R 5 are independent hydrogen atoms, halogen atoms and cyano groups, respectively. Represents an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, or an alkylene group or carbon having 3 to 6 carbon atoms in which R 2 and R 3 or R 4 and R 5 are linked to each other. Represents an alkylenedioxy group having 1 to 4 atoms. X represents a single bond, an acetal compound represented by -CH (OH) -group or -CH (OH) CH (OH) -group.
    Including
    The ratio (A) / (B) of the content (parts by mass) of the (A) triazine compound to the content (parts by mass) of the (B) acetal compound is 1/99 to 99/1. Clearing agent.
  2.  前記一般式(1)のAr、ArおよびArのうち少なくとも1つが、カルボニル基を含む置換基を有する請求項1記載の透明化剤。 The clearing agent according to claim 1, wherein at least one of Ar 1 , Ar 2 and Ar 3 of the general formula (1) has a substituent containing a carbonyl group.
  3.  前記一般式(2)中のR、R、R、RおよびRがそれぞれ独立に水素原子または炭素原子数1~4のアルキル基であり、Xが-CH(OH)-基である請求項1または2記載の透明化剤。 R 1 , R 2 , R 3 , R 4 and R 5 in the general formula (2) are independently hydrogen atoms or alkyl groups having 1 to 4 carbon atoms, and X is an −CH (OH) − group. The clearing agent according to claim 1 or 2.
  4.  ポリオレフィン系樹脂と、
     (A)下記一般式(1)、
    Figure JPOXMLDOC01-appb-I000003
    (一般式(1)中、Ar、ArおよびArは、それぞれ独立に、無置換のフェニル基または置換基を有するフェニル基を表す。)で表されるトリアジン化合物と、
     (B)下記一般式(2)、
    Figure JPOXMLDOC01-appb-I000004
    (一般式(2)中、Rは水素原子または炭素原子数1~4のアルキル基を表す。R、R、RおよびRはそれぞれ独立に水素原子、ハロゲン原子、シアノ基、炭素原子数1~4のアルキル基または炭素原子数1~4のアルコキシ基を表し、あるいはRおよびRまたはRおよびRが互いに連結して炭素原子数3~6のアルキレン基または炭素原子数1~4のアルキレンジオキシ基を表す。Xは単結合、-CH(OH)-基または-CH(OH)CH(OH)-基を表す。)で表されるアセタール化合物と、
    を含み、
     前記(A)トリアジン化合物の含有量(質量部)と前記(B)アセタール化合物の含有量(質量部)との比(A)/(B)が1/99~99/1であり、
     前記ポリオレフィン系樹脂100質量部に対する前記(A)トリアジン化合物および前記(B)アセタール化合物の合計含有量が0.001~10質量部であることを特徴とする樹脂組成物。
    Polyolefin resin and
    (A) The following general formula (1),
    Figure JPOXMLDOC01-appb-I000003
    (In the general formula (1), Ar 1 , Ar 2 and Ar 3 each independently represent an unsubstituted phenyl group or a phenyl group having a substituent.)
    (B) The following general formula (2),
    Figure JPOXMLDOC01-appb-I000004
    (In the general formula (2), R 1 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. R 2 , R 3 , R 4 and R 5 are independent hydrogen atoms, halogen atoms and cyano groups, respectively. Represents an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, or an alkylene group or carbon having 3 to 6 carbon atoms in which R 2 and R 3 or R 4 and R 5 are linked to each other. Represents an alkylenedioxy group having 1 to 4 atoms. X represents a single bond, an acetal compound represented by -CH (OH) -group or -CH (OH) CH (OH) -group.
    Including
    The ratio (A) / (B) of the content (parts by mass) of the (A) triazine compound to the content (parts by mass) of the (B) acetal compound is 1/99 to 99/1.
    A resin composition characterized in that the total content of the (A) triazine compound and the (B) acetal compound is 0.001 to 10 parts by mass with respect to 100 parts by mass of the polyolefin-based resin.
  5.  前記ポリオレフィン系樹脂が、ポリプロピレン系樹脂である請求項4記載の樹脂組成物。 The resin composition according to claim 4, wherein the polyolefin-based resin is a polypropylene-based resin.
  6.  請求項4または5記載の樹脂組成物を成形して得られることを特徴とする成形品。 A molded product obtained by molding the resin composition according to claim 4 or 5.
  7.  容器である請求項6記載の成形品。 The molded product according to claim 6, which is a container.
  8.  ポリオレフィン系樹脂に、
     (A)下記一般式(1)、
    Figure JPOXMLDOC01-appb-I000005
    (一般式(1)中、Ar、ArおよびArは、それぞれ独立に、無置換のフェニル基または置換基を有するフェニル基を表す。)で表されるトリアジン化合物と、
     (B)下記一般式(2)、
    Figure JPOXMLDOC01-appb-I000006
    (一般式(2)中、Rは水素原子または炭素原子数1~4のアルキル基を表す。R、R、RおよびRはそれぞれ独立に水素原子、ハロゲン原子、シアノ基、炭素原子数1~4のアルキル基または炭素原子数1~4のアルコキシ基を表し、あるいはRおよびRまたはRおよびRが互いに連結して炭素原子数3~6のアルキレン基または炭素原子数1~4のアルキレンジオキシ基を表す。Xは単結合、-CH(OH)-基または-CH(OH)CH(OH)-基を表す。)で表されるアセタール化合物と、
    を配合する工程を含み、
     前記(A)トリアジン化合物の配合量(質量部)と前記(B)アセタール化合物の配合量(質量部)との比(A)/(B)が1/99~99/1であり、
     前記ポリオレフィン系樹脂100質量部に対する前記(A)トリアジン化合物および前記(B)アセタール化合物の合計配合量が0.001~10質量部であることを特徴とする樹脂組成物の製造方法。
    For polyolefin resin
    (A) The following general formula (1),
    Figure JPOXMLDOC01-appb-I000005
    (In the general formula (1), Ar 1 , Ar 2 and Ar 3 each independently represent an unsubstituted phenyl group or a phenyl group having a substituent.)
    (B) The following general formula (2),
    Figure JPOXMLDOC01-appb-I000006
    (In the general formula (2), R 1 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. R 2 , R 3 , R 4 and R 5 are independent hydrogen atoms, halogen atoms and cyano groups, respectively. Represents an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, or an alkylene group or carbon having 3 to 6 carbon atoms in which R 2 and R 3 or R 4 and R 5 are linked to each other. Represents an alkylenedioxy group having 1 to 4 atoms. X represents a single bond, an acetal compound represented by -CH (OH) -group or -CH (OH) CH (OH) -group.
    Including the process of blending
    The ratio (A) / (B) of the compounding amount (parts by mass) of the (A) triazine compound to the compounding amount (parts by mass) of the (B) acetal compound is 1/99 to 99/1.
    A method for producing a resin composition, wherein the total amount of the (A) triazine compound and the (B) acetal compound is 0.001 to 10 parts by mass with respect to 100 parts by mass of the polyolefin resin.
  9.  ポリオレフィン系樹脂と(A)下記一般式(1)、
    Figure JPOXMLDOC01-appb-I000007
    (一般式(1)中、Ar、ArおよびArは、それぞれ独立に、無置換のフェニル基または置換基を有するフェニル基を表す。)で表されるトリアジン化合物とを含む樹脂組成物に(B)下記一般式(2)、
    Figure JPOXMLDOC01-appb-I000008
    (一般式(2)中、Rは水素原子または炭素原子数1~4のアルキル基を表す。R、R、RおよびRはそれぞれ独立に水素原子、ハロゲン原子、シアノ基、炭素原子数1~4のアルキル基または炭素原子数1~4のアルコキシ基を表し、あるいはRおよびRまたはRおよびRが互いに連結して炭素原子数3~6のアルキレン基または炭素原子数1~4のアルキレンジオキシ基を表す。Xは単結合、-CH(OH)-基または-CH(OH)CH(OH)-基を表す。)で表されるアセタール化合物を配合する工程を含み、
     前記(A)トリアジン化合物の配合量(質量部)と前記(B)アセタール化合物の配合量(質量部)との比(A)/(B)が1/99~99/1であり、
     前記ポリオレフィン系樹脂100質量部に対する前記(A)トリアジン化合物および前記(B)アセタール化合物の合計配合量が0.001~10質量部であることを特徴とする樹脂組成物の製造方法。
    Polyolefin resin and (A) General formula (1) below,
    Figure JPOXMLDOC01-appb-I000007
    (In the general formula (1), Ar 1 , Ar 2 and Ar 3 each independently represent an unsubstituted phenyl group or a phenyl group having a substituent.) A resin composition containing a triazine compound represented by the above. (B) The following general formula (2),
    Figure JPOXMLDOC01-appb-I000008
    (In the general formula (2), R 1 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. R 2 , R 3 , R 4 and R 5 are independent hydrogen atoms, halogen atoms and cyano groups, respectively. Represents an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, or an alkylene group or carbon having 3 to 6 carbon atoms in which R 2 and R 3 or R 4 and R 5 are linked to each other. It represents an alkylenedioxy group having 1 to 4 atoms. X represents a single bond, -CH (OH) -group or -CH (OH) CH (OH) -group). Including the process
    The ratio (A) / (B) of the compounding amount (parts by mass) of the (A) triazine compound to the compounding amount (parts by mass) of the (B) acetal compound is 1/99 to 99/1.
    A method for producing a resin composition, wherein the total amount of the (A) triazine compound and the (B) acetal compound is 0.001 to 10 parts by mass with respect to 100 parts by mass of the polyolefin resin.
  10.  ポリオレフィン系樹脂と(B)下記一般式(2)、
    Figure JPOXMLDOC01-appb-I000009
    (一般式(2)中、Rは水素原子または炭素原子数1~4のアルキル基を表す。R、R、RおよびRはそれぞれ独立に水素原子、ハロゲン原子、シアノ基、炭素原子数1~4のアルキル基または炭素原子数1~4のアルコキシ基を表し、あるいはRおよびRまたはRおよびRが互いに連結して炭素原子数3~6のアルキレン基または炭素原子数1~4のアルキレンジオキシ基を表す。Xは単結合、-CH(OH)-基または-CH(OH)CH(OH)-基を表す。)で表されるアセタール化合物とを含む樹脂組成物に、(A)下記一般式(1)、
    Figure JPOXMLDOC01-appb-I000010
    (一般式(1)中、Ar、ArおよびArは、それぞれ独立に、無置換のフェニル基または置換基を有するフェニル基を表す。)で表されるトリアジン化合物を配合する工程を含み、
     前記(A)トリアジン化合物の配合量(質量部)と前記(B)アセタール化合物の配合量(質量部)との比(A)/(B)が1/99~99/1であり、
     前記ポリオレフィン系樹脂100質量部に対する前記(A)トリアジン化合物および前記(B)アセタール化合物の合計配合量が0.001~10質量部であることを特徴とする樹脂組成物の製造方法。
    Polyolefin resin and (B) General formula (2) below,
    Figure JPOXMLDOC01-appb-I000009
    (In the general formula (2), R 1 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. R 2 , R 3 , R 4 and R 5 are independent hydrogen atoms, halogen atoms and cyano groups, respectively. Represents an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, or an alkylene group or carbon having 3 to 6 carbon atoms in which R 2 and R 3 or R 4 and R 5 are linked to each other. Represents an alkylenedioxy group having 1 to 4 atoms. X represents a single bond, an acetal compound represented by -CH (OH) -group or -CH (OH) CH (OH) -group. In the resin composition, (A) the following general formula (1),
    Figure JPOXMLDOC01-appb-I000010
    (In the general formula (1), Ar 1 , Ar 2 and Ar 3 each independently represent an unsubstituted phenyl group or a phenyl group having a substituent.) Including a step of blending a triazine compound represented by the above. ,
    The ratio (A) / (B) of the compounding amount (parts by mass) of the (A) triazine compound to the compounding amount (parts by mass) of the (B) acetal compound is 1/99 to 99/1.
    A method for producing a resin composition, wherein the total amount of the (A) triazine compound and the (B) acetal compound is 0.001 to 10 parts by mass with respect to 100 parts by mass of the polyolefin resin.
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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06218A (en) * 1992-06-22 1994-01-11 Chisso Corp Medical tool
CN102585353A (en) * 2011-01-13 2012-07-18 绵阳鸿琪新材料科技有限公司 Impact-resistance and low temperature-resistance transparent polypropylene composition and preparation method for transparent polypropylene composition
JP2013209662A (en) * 2013-05-31 2013-10-10 Adeka Corp Transparentizing agent composition and polyolefin resin composition containing the same
WO2019084360A1 (en) * 2017-10-27 2019-05-02 W.R. Grace & Co.-Conn. Polyolefin polymers with increased melt strength
WO2020241503A1 (en) * 2019-05-24 2020-12-03 株式会社Adeka Resin composition and molded article thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06218A (en) * 1992-06-22 1994-01-11 Chisso Corp Medical tool
CN102585353A (en) * 2011-01-13 2012-07-18 绵阳鸿琪新材料科技有限公司 Impact-resistance and low temperature-resistance transparent polypropylene composition and preparation method for transparent polypropylene composition
JP2013209662A (en) * 2013-05-31 2013-10-10 Adeka Corp Transparentizing agent composition and polyolefin resin composition containing the same
WO2019084360A1 (en) * 2017-10-27 2019-05-02 W.R. Grace & Co.-Conn. Polyolefin polymers with increased melt strength
WO2020241503A1 (en) * 2019-05-24 2020-12-03 株式会社Adeka Resin composition and molded article thereof

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