WO2013133352A1 - ポリエステル系樹脂組成物及びその製造方法、並びに該樹脂組成物を用いた成形体 - Google Patents
ポリエステル系樹脂組成物及びその製造方法、並びに該樹脂組成物を用いた成形体 Download PDFInfo
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
- C08L67/03—Polyesters derived from dicarboxylic acids and dihydroxy compounds the dicarboxylic acids and dihydroxy compounds having the carboxyl- and the hydroxy groups directly linked to aromatic rings
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- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D1/00—Containers having bodies formed in one piece, e.g. by casting metallic material, by moulding plastics, by blowing vitreous material, by throwing ceramic material, by moulding pulped fibrous material, by deep-drawing operations performed on sheet material
- B65D1/02—Bottles or similar containers with necks or like restricted apertures, designed for pouring contents
- B65D1/0207—Bottles or similar containers with necks or like restricted apertures, designed for pouring contents characterised by material, e.g. composition, physical features
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- C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
- C08F212/02—Monomers containing only one unsaturated aliphatic radical
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- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/32—Esters containing oxygen in addition to the carboxy oxygen containing epoxy radicals
- C08F220/325—Esters containing oxygen in addition to the carboxy oxygen containing epoxy radicals containing glycidyl radical, e.g. glycidyl (meth)acrylate
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- C08J3/00—Processes of treating or compounding macromolecular substances
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- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/08—Copolymers of styrene
- C08L25/14—Copolymers of styrene with unsaturated esters
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- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur, or oxygen atoms in addition to the carboxy oxygen
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D1/00—Containers having bodies formed in one piece, e.g. by casting metallic material, by moulding plastics, by blowing vitreous material, by throwing ceramic material, by moulding pulped fibrous material, by deep-drawing operations performed on sheet material
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- C—CHEMISTRY; METALLURGY
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2367/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
- C08J2367/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
- C08J2367/03—Polyesters derived from dicarboxylic acids and dihydroxy compounds the dicarboxylic acids and dihydroxy compounds having the hydroxy and the carboxyl groups directly linked to aromatic rings
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- C08J2477/00—Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers
- C08J2477/06—Polyamides derived from polyamines and polycarboxylic acids
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
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- C—CHEMISTRY; METALLURGY
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/10—Transparent films; Clear coatings; Transparent materials
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/14—Gas barrier composition
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08L2203/00—Applications
- C08L2203/16—Applications used for films
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- C—CHEMISTRY; METALLURGY
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2310/00—Masterbatches
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/06—Polyamides derived from polyamines and polycarboxylic acids
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
- Y10T428/1397—Single layer [continuous layer]
Definitions
- the present invention relates to a polyester-based resin composition and a molded body using the resin composition, and more specifically, a resin composition containing a specific polyester resin as a main component and containing a specific polyamide resin, and the resin composition. It relates to the molded body used.
- polyesters represented by polyethylene terephthalate (PET) are transparent, mechanical performance, melt stability, aroma retention, recycling It is widely used for various packaging materials such as films, sheets and hollow containers.
- PET polyethylene terephthalate
- polyester has insufficient gas barrier properties against oxygen, carbon dioxide gas, etc.
- the range of use of packaging containers made of polyester has been limited.
- As a means for improving the gas barrier property of polyester a method of depositing aluminum oxide or silicon oxide on a molded body or packaging container made of polyester, or a resin having a gas barrier performance higher than that of polyester on a molded body or packaging container made of polyester. The method of apply
- coating etc. are mentioned.
- there are problems such as requiring a complicated manufacturing process and recyclability and mechanical performance being impaired, the range of use has been limited.
- thermoplastic resin having a high gas barrier property As a means for simply improving the gas barrier property of the polyester while solving the above problems, there is a method of melt-mixing a thermoplastic resin having a high gas barrier property into the polyester resin.
- a resin having a high gas barrier property is an ethylene-vinyl alcohol copolymer resin, but the ethylene-vinyl alcohol copolymer resin has poor compatibility with polyesters due to the characteristics of its molecular structure.
- the resin composition obtained by mixing the resin is cloudy and has the disadvantage of impairing the transparency characteristic of polyester.
- ethylene-vinyl alcohol copolymer resins deteriorate rapidly when exposed to processing temperatures suitable for polyethylene terephthalate, which is the most widely used polyester, and may cause foreign matters such as gels and koges.
- Examples of the gas barrier resin other than the ethylene-vinyl alcohol copolymer include polyamides represented by nylon 6, nylon 66 and the like, and in particular, a diamine component mainly composed of metaxylylenediamine and adipic acid as a major component.
- Polymetaxylylene adipamide (MXD6) obtained by polymerizing a dicarboxylic acid component to be produced is a polyamide having particularly excellent gas barrier properties, and polyethylene terephthalate, glass transition temperature, melting point, crystallinity, which are particularly widely used among polyesters Therefore, the processability of the polyester is not impaired. From this, it can be said that polymetaxylylene adipamide is a very suitable resin as a material for improving the gas barrier property of polyester.
- JP 58-160344 A Japanese Patent Laid-Open No. 03-130125 JP 58-90033 A Japanese Patent Laid-Open No. 08-183092 JP 2011-37989 A JP 2011-132394 A
- the problem to be solved by the present invention is to provide a polyester resin composition excellent in gas barrier properties and transparency, and a molded body using the resin composition.
- the inventors have a polyester resin as a main component, and by blending a specific epoxy functional polymer with a resin component containing a specific polyamide resin, the gas barrier property is excellent. It was also found that a resin composition with improved transparency can be provided. In particular, it has been found that transparency is excellent when a molded body is drawn using the resin composition. The present invention has been completed based on such findings.
- this invention relates to the following polyester-type resin compositions, its manufacturing method, and the molded object using this resin composition.
- Step 1 A master batch (X) is prepared by melt-kneading 10 to 40 parts by mass of an epoxy-functional polymer (C) to 100 parts by mass of a polyester resin (A) containing an aromatic dicarboxylic acid unit and a diol unit. Process.
- Step 2 Polyester resin (A) containing aromatic dicarboxylic acid unit and diol unit (A) 80 to 98% by mass, diamine unit containing metaxylylenediamine unit 70 mol% or more, and ⁇ , ⁇ -aliphatic dicarboxylic acid unit
- the master batch (X) obtained in step 1 is added in an amount of 0.055 to 1.5 with respect to 100 parts by mass of the resin component containing 20 to 2% by mass of the polyamide resin (B) containing 70 mol% or more of the dicarboxylic acid unit.
- the molded resin of the present invention having at least one layer composed of the polyester resin composition of the present invention and the resin composition is excellent in gas barrier properties and transparency.
- the stretched molded article is excellent in transparency.
- the polyester resin (A) used in the present invention contains an aromatic dicarboxylic acid unit and a diol unit.
- the aromatic dicarboxylic acid unit is preferably 70 mol% or more, more preferably 80 mol% or more, and still more preferably 90 to 100 mol% from the viewpoint of the crystallinity of the polyester resin and the ease of drying before use. Contains mol%.
- the diol unit preferably contains an aliphatic glycol unit having 2 to 4 carbon atoms in an amount of 70 mol% or more, more preferably 80 mol% or more, and further preferably 90 to 100 mol%.
- aromatic dicarboxylic acids that can be used in addition to terephthalic acid and its derivatives that can constitute the aromatic dicarboxylic acid unit of the polyester resin (A) include aromatics such as benzene, naphthalene, diphenyl, oxydiphenyl, sulfonyldiphenyl, and methylenediphenyl. Dicarboxylic acids having a nucleus and derivatives thereof can be used.
- isophthalic acid, 2,6-naphthalenedicarboxylic acid, 1,5-naphthalenedicarboxylic acid, naphthalenedicarboxylic acid such as 2,7-naphthalenedicarboxylic acid, 4,4′-biphenyldicarboxylic acid, 3,4′-biphenyldicarboxylic acid Acids and the like and derivatives thereof are preferred, and among these, isophthalic acid, 2,6-naphthalenedicarboxylic acid and derivatives thereof are more preferably used.
- the proportion is 1 to 10 mol%, preferably 1 to 8 mol%, more preferably 1 to 6 mol%, based on the total amount of the dicarboxylic acid component.
- a copolymer resin obtained by adding the above-mentioned amount of isophthalic acid as a dicarboxylic acid component has a low crystallization rate and can improve moldability.
- dicarboxylic acids having an aromatic nucleus in which a sulfonic acid metal base is bonded to a benzene, naphthalene, diphenyl, oxydiphenyl, sulfonyldiphenyl, or methylenediphenyl nucleus, and these derivatives can also be used as the dicarboxylic acid constituting the polyester resin (A).
- alkali metal ions such as lithium, sodium and potassium as alkaline metal ions of sulfonate, alkaline earth metal ions such as magnesium and calcium, zinc, sulfophthalic acid, sulfoterephthalic acid, sulfoisophthalic acid as aromatic acid nuclei, 4 -Dicarboxylic acid compounds obtained by combining sulfonaphthalene-2,7-dicarboxylic acid and derivatives thereof, among which metal salts of sulfoisophthalic acid such as sodium 5-sulfoisophthalate and zinc 5-sulfoisophthalate and derivatives thereof Is preferably used.
- the ratio of these dicarboxylic acids is preferably 0.01 to 2 mol%, more preferably 0.03 to 1.5 mol%, still more preferably 0.06 to 1 mol, based on all dicarboxylic acids. 0.0 mol%. By setting it as this range, compatibility can be improved, without impairing the characteristic of a polyester resin (A).
- aliphatic dicarboxylic acids such as adipic acid, azelaic acid, sebacic acid
- monocarboxylic acids such as benzoic acid, propionic acid, butyric acid, trimellitic acid, pyromellitic acid, etc.
- Carboxylic acid anhydrides such as monovalent carboxylic acid, trimellitic anhydride and pyromellitic anhydride can be used.
- the at least one glycol selected from aliphatic glycols having 2 to 4 carbon atoms that can constitute the diol unit of the polyester resin (A) ethylene glycol and butylene glycol are preferably used, and ethylene glycol is particularly preferably used.
- the diol component that can be used in addition to the aliphatic glycol having 2 to 4 carbon atoms include 1,4-cyclohexanedimethanol, 1,6-hexanediol, and the like, and ester-forming derivatives thereof.
- monoalcohols such as butyl alcohol, hexyl alcohol and octyl alcohol, polyhydric alcohols such as trimethylolpropane, glycerin and pentaerythritol, diol components having a cyclic acetal skeleton, etc. are used within a range not impairing the effects of the present invention. You can also.
- the polyester resin (A) is obtained by polymerizing an aromatic dicarboxylic acid and a diol, and a known method such as a direct esterification method or a transesterification method can be applied to the polyester resin (A).
- a known method such as a direct esterification method or a transesterification method can be applied to the polyester resin (A).
- the polycondensation catalyst during the production of polyester include known antimony compounds such as antimony trioxide and antimony pentoxide, and germanium compounds such as germanium oxide.
- polyesters in the present invention include polyethylene terephthalate, ethylene terephthalate-isophthalate copolymer, ethylene-1,4-cyclohexanedimethylene-terephthalate copolymer, polyethylene-2,6-naphthalene dicarboxylate, ethylene- There are 2,6-naphthalenedicarboxylate-terephthalate copolymer and ethylene-terephthalate-4,4′-biphenyldicarboxylate copolymer.
- Particularly preferred polyesters are polyethylene terephthalate and ethylene terephthalate-isophthalate copolymer.
- the polyester resin (A) used in the present invention is preferably dried to a moisture content in the polymer of 200 ppm or less, preferably 100 ppm or less, more preferably 50 ppm or less before use.
- the intrinsic viscosity is in the range of 0.6 to 2.0 dl / g
- the molecular weight of the polyester is sufficiently high and the viscosity at the time of melting is not too high. Can be easily produced, and can exhibit the mechanical properties required as a structure.
- the polyamide resin (B) used for this invention provides the effect which improves the gas barrier property of a polyester resin (A).
- the diamine unit in the polyamide resin (B) contains a metaxylylenediamine unit of 70 mol% or more, preferably 80 mol% or more, more preferably 90 to 100 mol%.
- the gas barrier property of the polyamide obtained by using metaxylylenediamine as the main component of the diamine unit can be improved efficiently.
- Diamines that can be used in addition to metaxylylenediamine include paraxylylenediamine, 1,3-bis (aminomethyl) cyclohexane, 1,4-bis (aminomethyl) cyclohexane, tetramethylenediamine, hexamethylenediamine, and nonanemethylenediamine. , 2-methyl-1,5-pentanediamine and the like, but are not limited thereto.
- the dicarboxylic acid unit in the polyamide resin (B) contains ⁇ , ⁇ -aliphatic dicarboxylic acid in an amount of 70 mol% or more, preferably 75 mol% or more, more preferably 80 to 100 mol%.
- ⁇ , ⁇ -aliphatic dicarboxylic acid By setting the content of ⁇ , ⁇ -aliphatic dicarboxylic acid to 70 mol% or more, it is possible to avoid a decrease in gas barrier properties and an excessive decrease in crystallinity.
- Examples of the ⁇ , ⁇ -aliphatic dicarboxylic acid include suberic acid, adipic acid, azelaic acid, sebacic acid and the like, and adipic acid and sebacic acid are preferably used.
- dicarboxylic acid units other than ⁇ , ⁇ -aliphatic dicarboxylic acids include alicyclic dicarboxylic acids such as 1,3-cyclohexanedicarboxylic acid and 1,4-cyclohexanedicarboxylic acid, terephthalic acid, isophthalic acid, orthophthalic acid, xylylene diene
- aromatic dicarboxylic acids such as carboxylic acid and naphthalenedicarboxylic acid, but are not limited thereto.
- the units constituting the polyamide resin (B) may be lactams such as ⁇ -caprolactam and laurolactam, aminocaproic acid, aminoundecanoic acid as long as the effects of the present invention are not impaired.
- lactams such as ⁇ -caprolactam and laurolactam
- aminocaproic acid aminoundecanoic acid as long as the effects of the present invention are not impaired.
- Aliphatic aminocarboxylic acids such as para-aminomethylbenzoic acid and the like can also be used as copolymerized units.
- the polyamide resin (B) is produced by a melt polycondensation (melt polymerization) method.
- the melt polycondensation method for example, there is a method in which a nylon salt composed of diamine and dicarboxylic acid is heated in the presence of water under pressure and polymerized in a molten state while removing added water and condensed water. It can also be produced by a method in which diamine is directly added to a molten dicarboxylic acid and polycondensed. In this case, in order to keep the reaction system in a uniform liquid state, diamine is continuously added to the dicarboxylic acid, while the reaction system is heated up so that the reaction temperature does not fall below the melting point of the generated oligoamide and polyamide. The polycondensation proceeds.
- a phosphorus atom-containing compound may be added in order to obtain an effect of promoting an amidation reaction and an effect of preventing coloring during polycondensation.
- phosphorus atom-containing compounds include dimethylphosphinic acid, phenylmethylphosphinic acid, hypophosphorous acid, sodium hypophosphite, potassium hypophosphite, lithium hypophosphite, ethyl hypophosphite, phenylphosphonous acid, Sodium phenylphosphonite, potassium phenylphosphonite, lithium phenylphosphonite, ethyl phenylphosphonite, phenylphosphonic acid, ethylphosphonic acid, sodium phenylphosphonate, potassium phenylphosphonate, lithium phenylphosphonate, phenylphosphonic acid Examples include diethyl, sodium ethylphosphonate, potassium ethylphosphonate, phosphorous acid,
- hypophosphorous Hypophosphite metal salts such as sodium, potassium hypophosphite, lithium hypophosphite and the like are preferably used because they have a high effect of promoting amidation reaction and are excellent in anti-coloring effect, especially sodium hypophosphite.
- the phosphorus atom-containing compounds that can be used in the present invention are not limited to these compounds.
- the amount of the phosphorus atom-containing compound added to the polycondensation system of the polyamide resin (B) is preferably 1 to 500 ppm, more preferably 5 to 450 ppm in terms of the phosphorus atom concentration in the polyamide resin (B). Yes, more preferably 10 to 400 ppm.
- an alkali metal compound in combination with the phosphorus atom-containing compound.
- a sufficient amount of the phosphorus atom-containing compound needs to be present, but in some cases, the gelation of the polyamide may be accelerated, so the amidation reaction rate is adjusted. Therefore, it is preferable to coexist an alkali metal compound or an alkaline earth metal compound.
- lithium hydroxide, sodium hydroxide, potassium hydroxide, rubidium hydroxide, cesium hydroxide, magnesium hydroxide, calcium hydroxide, barium hydroxide and other alkali metal / alkaline earth metal hydroxides lithium acetate
- Examples include sodium acetate, potassium acetate, rubidium acetate, cesium acetate, magnesium acetate, calcium acetate, barium acetate, and other alkali metal / alkaline earth metal acetates, etc., but these compounds can be used without limitation. .
- the value obtained by dividing the number of moles of the compound by the number of moles of the phosphorus atom-containing compound should be 0.5 to 2.0. Is more preferably 0.6 to 1.8, and still more preferably 0.7 to 1.5. By setting it as the above-mentioned range, it becomes possible to suppress the formation of gel while obtaining the amidation reaction promoting effect by the phosphorus atom-containing compound.
- the polyamide resin (B) obtained by melt polycondensation is once taken out, pelletized, and dried before use.
- solid phase polymerization may be performed.
- a heating device used in drying or solid phase polymerization a continuous heating drying device, a rotary drum type heating device called a tumble dryer, a conical dryer, a rotary dryer or the like, and a rotary blade inside a nauta mixer are used.
- a conical heating apparatus provided with can be used suitably, a well-known method and apparatus can be used without being limited to these.
- the rotating drum type heating device can seal the inside of the system, and it is easy to proceed with polycondensation in a state where oxygen causing coloring is removed.
- the rotating drum type heating device can seal the inside of the system, and it is easy to proceed with polycondensation in a state where oxygen causing coloring is removed.
- the polyamide resin (B) obtained through the above-mentioned steps has little coloration and little gel.
- b in the color difference test of JIS-K-7105 is preferably used, more preferably 3 or less, and still more preferably 1 or less.
- the relative viscosity is generally used.
- a preferred relative viscosity is 1.5 to 4.2, more preferably 1.6 to 4.0, and still more preferably 1.7 to 3.8.
- the terminal amino group concentration of the polyamide resin (B) used in the present invention is preferably 10 to 40 ⁇ eq / g, more preferably 12 to 35 ⁇ eq / g, and further preferably 15 to 30 ⁇ eq / g. .
- the content of metaxylylenediamine remaining in the polyamide resin (B) is preferably 10 ppm or less, more preferably 5 ppm or less, and further preferably 1 ppm.
- the residual amount of metaxylylenediamine is 10 ppm or less, yellowing of the appearance caused by the reaction between the acetaldehyde generated from the polyester resin (A) and the terminal amino group is suppressed.
- the means for reducing the content of metaxylylenediamine to 10 ppm or less include a method of heating the polyamide after polymerization under reduced pressure, a method of melting it with an extruder and the like, and reducing the pressure inside the system. Various methods can be used without being limited to the above.
- an oligomer composed of a dicarboxylic acid unit and a diamine unit may be mixed.
- a monomer (cyclic monomer) in which metaxylylenediamine and adipic acid are cyclized may float on the surface of the molded container during melt processing and impair the appearance of the container.
- the amount of the cyclic monomer contained in the polyamide resin (B) is preferably 1% by mass or less, more preferably 0.8% by mass or less, and still more preferably 0.5% by mass or less. is there.
- the polyamide resin (B) is washed with water, treated at a high temperature and under a high vacuum, or removed by reducing the pressure inside the extrusion apparatus during melt extrusion.
- the present invention is not limited to these methods, and known methods for removing low molecular weight or volatile components can be appropriately employed.
- the method for measuring the content of the cyclic monomer in the present invention can be obtained by pulverizing polyamide by freeze pulverization, extracting it at 80 ° C. for 1 hour with methanol as a solvent, and analyzing it by liquid chromatography. .
- the mass ratio of the polyester resin (A) to the polyamide resin (B) is mechanical strength and gas barrier property. From the viewpoint, when the total mass of the polyester resin (A) and the polyamide resin (B) is 100, it is 80 to 98/20 to 2, preferably 82 to 97/18 to 3, more preferably 85 to 96. / 15 to 4, more preferably 87 to 95/13 to 5.
- the resin component of the polyester resin composition of the present invention may contain a resin other than the polyester resin (A) and the polyamide resin (B) as long as the effects of the present invention are not impaired.
- a resin other than the polyester resin (A) and the polyamide resin (B) examples include nylon 6 and nylon 66, various polyamides such as amorphous nylon using aromatic dicarboxylic acid as a monomer, modified resins thereof, polyolefin and modified resins thereof, and styrene in the skeleton. And the like.
- Epoxy functional polymer (C) The epoxy functional polymer (C) used in the present invention has at least a styrene unit represented by the following general formula (c1) and a glycidyl (meth) acrylate unit represented by the following general formula (c2), preferably Furthermore, it has a (meth) acrylate unit represented by the following general formula (c3).
- R 1 to R 5 each independently represents a hydrogen atom or an alkyl group having 1 to 12 carbon atoms
- R 6 represents an alkyl group having 1 to 12 carbon atoms.
- R 1 to R 5 each independently represents a hydrogen atom or an alkyl group having 1 to 12 carbon atoms, and when R 1 to R 5 are alkyl groups, Is 1 to 12, preferably 1 to 6, and may be linear, branched or cyclic. Specific examples of the alkyl group include a methyl group, an ethyl group, and a propyl group, and a methyl group is particularly preferable.
- R 6 represents an alkyl group having 1 to 12 carbon atoms, preferably 1 to 6 carbon atoms, and may be linear, branched or cyclic.
- alkyl group examples include a methyl group, an ethyl group, and a propyl group, and a methyl group is particularly preferable.
- R 4 in the general formula (c2) is a methyl group
- R 5 in the general formula (c3) is a methyl group
- a polyester resin composition containing the epoxy functional polymer Since the molded object which consists of is excellent in transparency, it is especially preferable.
- the number x of styrene units represented by the general formula (c1) and the number y of glycidyl (meth) acrylate units represented by the general formula (c2) contained in the epoxy functional polymer are each independently 1 From the viewpoint of transparency, y is preferably 2 to 30, and more preferably 4 to 25. x + y is preferably 10 to 70, more preferably 15 to 60.
- the number y of acrylate units and the number z of (meth) acrylate units represented by the general formula (c3) are each independently 1 to 20, and y is preferably 2 to 20, from the viewpoint of transparency. More preferably, it is 3-10.
- x + z is preferably greater than 10.
- the respective structural units can be bonded in any order, and the epoxy functional polymer represented by the general formula (I) may be a block copolymer or a random copolymer.
- epoxy functional polymer represented by the general formula (I) Commercially available products can be used as the epoxy functional polymer represented by the general formula (I), and examples thereof include “Joncry ADR” (trade name) manufactured by BASF.
- the epoxy functional polymer (C) is contained in an amount of 0.005 to 0.1 parts by mass, preferably 0.02 to 0.05 parts by mass, with respect to 100 parts by mass of the resin component. If it is less than 0.005 parts by mass, the transparency cannot be improved, and if it exceeds 0.1 parts by mass, the melt viscosity of the resulting polyester resin composition is remarkably increased and there is a concern of gelation. Absent.
- the transparency can be improved without deteriorating the gas barrier property. Can be improved.
- the mechanism of action is not clear, but the polymer end groups of the polyester resin (A) and the polyamide resin (B) are chemically reacted with the epoxy functional polymer (C) and bonded to each other. It is estimated that the island of polyamide resin (B) can be finely dispersed in the sea.
- the resin composition of the present invention includes an antioxidant, a matting agent, a heat stabilizer, a weather stabilizer, a UV absorber, a nucleating agent, a plasticizer, a flame retardant, and an antistatic agent as long as the effects of the present invention are not impaired.
- Additives such as anti-coloring agents, lubricants and anti-gelling agents, clays such as layered silicates, nanofillers, and the like can also be blended.
- a cobalt compound can be blended with the resin composition of the present invention for the purpose of inducing an oxidation reaction of the polyamide resin (B) and enhancing the oxygen absorption function.
- cobalt carboxylates such as cobalt octoate, cobalt naphthenate, cobalt acetate, and cobalt stearate are preferably used.
- the amount of the cobalt compound added is preferably 10 to 1000 ppm, more preferably 30 to 600 ppm, and still more preferably 50 to 50 ppm as the concentration of cobalt metal with respect to the total mass of the resin composition from the viewpoint of providing an effective oxygen absorption function. 400 ppm.
- the above-described cobalt compound functions not only as a polyamide resin (B) but also as a catalyst for an oxidation reaction of an organic compound having an unsaturated carbon bond or a compound having secondary or tertiary hydrogen in the molecule. Therefore, in order to further enhance the oxygen absorption function, the resin composition of the present invention includes polymers of unsaturated hydrocarbons such as polybutadiene and polyisoprene or oligomers thereof, xylylenediamine in addition to the above-described cobalt compound. And various compounds exemplified by a compound having a functional group added to enhance the compatibility between the compound and the polyester.
- the method for producing the polyester resin composition is not particularly limited.
- a desired resin composition can be obtained by melt-kneading a polyester resin (A), a polyamide resin (B), and an epoxy functional polymer (C) in an extruder.
- a polyester resin (A) or polyamide resin (B) and an epoxy functional polymer (C) are melt-kneaded in advance to prepare a master batch, and the polyester resin (A) and polyamide resin (B) are melted.
- Step 1 A master batch (X) is prepared by melt-kneading 10 to 40 parts by mass of an epoxy-functional polymer (C) to 100 parts by mass of a polyester resin (A) containing an aromatic dicarboxylic acid unit and a diol unit. Process.
- Step 2 Polyester resin (A) containing aromatic dicarboxylic acid unit and diol unit (A) 80 to 98% by mass, diamine unit containing metaxylylenediamine unit 70 mol% or more, and ⁇ , ⁇ -aliphatic dicarboxylic acid unit
- the master batch (X) obtained in step 1 is added in an amount of 0.055 to 1.5 with respect to 100 parts by mass of the resin component containing 20 to 2% by mass of the polyamide resin (B) containing 70 mol% or more of the dicarboxylic acid unit.
- the polyester-based resin composition of the present invention can be used in various applications that require gas barrier properties such as various packaging materials and industrial materials, and can be formed into molded articles such as films, sheets, and thin-walled hollow containers.
- the molded article of the present invention has at least one layer made of the polyester resin composition.
- the molded body of the present invention may have a single-layer structure made of the polyester resin composition, and another thermoplastic resin layer (for example, a polyester resin layer or an adhesive) is attached to at least one of the layers made of the polyester resin composition. Resin layer) or a multilayer structure in which two or more polyester resin composition layers are laminated.
- the film or sheet can be formed by extruding the resin composition melted through a T die, a circular die or the like from an extruder.
- the obtained film can be processed into a stretched film by stretching.
- a bottle-shaped packaging container can be obtained by injecting a molten resin composition into a mold from an injection molding machine to produce a preform, heating to a stretching temperature, and blow-drawing.
- Containers such as trays and cups can be obtained by injecting a molten resin composition into a mold from an injection molding machine, or by forming a sheet by a molding method such as vacuum molding or pressure molding. .
- a molded body using the resin composition of the present invention can be produced through various methods regardless of the production method described above.
- the haze is preferably 5% or less, more preferably 4% or less.
- the haze becomes like this. Preferably it is 9.5% or less, More preferably, it is 9.0% or less, More preferably, it is 8.5% or less.
- the measuring method of haze is as having described in the Example mentioned later.
- the packaging container using the polyester resin composition of the present invention can store and store various articles.
- various articles such as beverages, seasonings, cereals, liquids and solid processed foods that require aseptic filling or heat sterilization, chemicals, liquid daily necessities, pharmaceuticals, semiconductor integrated circuits, and electronic devices can be stored. it can.
- the present invention will be described in more detail based on examples, but the present invention is not limited to these examples.
- the material used for the Example and the comparative example, the analysis / measurement method, and the manufacturing method of a molded object are as follows.
- Polyester resin The following materials were used in Examples and Comparative Examples.
- Polyester resin The following PET resins were used. In use, pellets dried at 150 ° C. for 6 hours in a dehumidifying dryer were used.
- Epoxy functional polymer (C), masterbatch (X) An epoxy functional polymer (manufactured by BASF, trade name: “Joncry ADR-4368”, weight average molecular weight 6,800, epoxy value 285 g / mol) was used.
- the polymer used in this example has at least the units represented by the general formulas (c1) and (c2), R 1 to R 3 are each a hydrogen atom, R 4 is a methyl group, and x is 31 to 34, y is 22-25.
- a resin composition (masterbatch (X)) obtained by melt-kneading 30 parts by mass of an epoxy functional polymer (C) with 100 parts by mass of a PET resin (A) is obtained by using a vacuum dryer. What was dried at 5 ° C. for 5 hours was used.
- Terminal carboxyl group concentration [COOH] mmol / kg) 0.5 g of polyamide resin was precisely weighed, and polyamide was dissolved in 30 ml of benzyl alcohol with stirring at 160 to 180 ° C. in a nitrogen stream. After the polyamide was completely dissolved, it was cooled to 80 ° C. under a nitrogen stream, 10 ml of methanol was added with stirring, and neutralization titration with an aqueous N / 100 sodium hydroxide solution was performed.
- Oxygen permeability measurement of polyester-based container About an unstretched sheet and a biaxially stretched film, an oxygen permeability measuring device (manufactured by MOCON, trade name: “OX-TRAN 2 / 21SH”) is used. The oxygen permeability of the 0.3 mm sheet and 35 ⁇ m film was measured under the conditions of 60 ° C. and 60% RH. The lower the value, the less oxygen permeation is preferable.
- an oxygen transmission rate measuring device manufactured by MOCON, trade name: “OX-TRAN 2/21”
- the internal humidity of the container is 100% RH
- the external humidity 50% RH
- the temperature is 23 ° C.
- the oxygen permeability was measured under the conditions. The lower the value, the less oxygen permeation is preferable.
- master batch (X) prepared in advance 0.0231 part by mass as epoxy functional polymer (C)
- Example 2 Unstretched sheet and biaxially stretched film in the same manner as in Example 1 except that the addition amount of the master batch (X) was changed to 0.2 parts by mass (0.0462 parts by mass as the epoxy functional polymer (C)). Got.
- Comparative Example 1 An unstretched sheet and a biaxially stretched film were obtained in the same manner as in Example 1 except that the master batch (X) was not added.
- Table 1 shows the haze and oxygen permeability of unstretched sheets and biaxially stretched films obtained in Examples and Comparative Examples.
- the unstretched sheet and biaxially stretched film of Examples 1 and 2 to which a predetermined amount of the epoxy functional polymer (C) was added were the unstretched sheet and the biaxially stretched film of Comparative Example 1 to which the epoxy functional polymer (C) was not added.
- the transparency could be greatly improved while maintaining the gas barrier property.
- the biaxially stretched film is excellent in transparency without increasing haze.
- Example 4 A single layer bottle was obtained in the same manner as in Example 3 except that the addition amount of the master batch (X) was changed to 0.2 parts by mass (0.0462 parts by mass as the epoxy functional polymer (C)).
- Comparative Example 2 A single-layer bottle was obtained in the same manner as in Example 3 except that the master batch (X) was not added.
- Comparative Example 3 A single layer bottle was obtained in the same manner as in Example 3 except that the addition amount of the master batch (X) was changed to 0.005 parts by mass (0.0012 parts by mass as the epoxy functional polymer (C)).
- Table 2 shows the haze and oxygen permeability of the single layer bottles obtained in Examples and Comparative Examples.
- the single-layer bottles of Examples 3 and 4 to which a predetermined amount of the epoxy-functional polymer (C) was added had a gas barrier property compared to the single-layer bottle of Comparative Example 2 to which no epoxy-functional polymer (C) was added. Transparency could be greatly improved while maintaining. Also, the single-layer bottle of Comparative Example 3 in which the epoxy functional polymer (C) was slightly added, unlike the single-layer bottles of Examples 3 and 4, could not improve the transparency.
- Example 5 A single layer bottle was obtained in the same manner as in Example 3 except that PET2 was used as the polyester resin (A).
- Example 6 A single layer bottle was obtained in the same manner as in Example 4 except that PET2 was used as the polyester resin (A).
- Comparative Example 4 A single-layer bottle was obtained in the same manner as in Comparative Example 2 except that PET2 was used as the polyester resin (A).
- Table 3 shows the haze and oxygen permeability of the single-layer bottles obtained in Examples and Comparative Examples.
- the single-layer bottles of Examples 5 and 6 to which a predetermined amount of the epoxy-functional polymer (C) was added had a gas barrier property as compared with the single-layer bottle of Comparative Example 4 to which no epoxy-functional polymer (C) was added. Transparency could be greatly improved while maintaining.
- the polyester-based resin composition and molded body of the present invention can achieve both excellent gas barrier properties and transparency, and can be used for sheets, films, packaging containers, other various molded products, and composite materials (for example, multilayer films, multilayer containers). ) And so on.
Abstract
Description
ポリエステルのガスバリア性を改善する手段としては、酸化アルミニウムや酸化ケイ素をポリエステルからなる成形体や包装容器に蒸着する方法や、ポリエステルよりも高いガスバリア性能を有する樹脂をポリエステルからなる成形体や包装容器に塗布する方法等が挙げられる。しかし、複雑な製造工程を必要としたり、リサイクル性や機械的性能が損なわれたりする等の問題点があるため、その利用範囲は限定されたものであった。
PETとMXD6との混合物は、ポリエチレンテレフタレートの成形加工条件をほぼそのまま適用して加工できるため、フィルムやボトル等、様々な包装材料への適用が開示されている(例えば、特許文献1~6参照)。
しかしながら、PETとMXD6とのブレンドからなる従来の成形体は、未延伸の状態では比較的透明性を有するが、延伸するとヘイズ(曇り値)が増加し、透明性が低下するという問題を有する。
<1>芳香族ジカルボン酸単位とジオール単位とを含むポリエステル樹脂(A)80~98質量%、及びメタキシリレンジアミン単位を70モル%以上含むジアミン単位と、α,ω-脂肪族ジカルボン酸単位を70モル%以上含むジカルボン酸単位とを含むポリアミド樹脂(B)20~2質量%を含む樹脂成分100質量部に対し、下記一般式(c1)で表されるスチレン単位及び下記一般式(c2)で表されるグリシジル(メタ)アクリレート単位を含むエポキシ官能性ポリマー(C)0.005~0.1質量部を含有する、ポリエステル系樹脂組成物。
<2>下記工程1及び2を含む、上記<1>に記載のポリエステル系樹脂組成物の製造方法。
工程1:芳香族ジカルボン酸単位とジオール単位とを含むポリエステル樹脂(A)100質量部に対してエポキシ官能性ポリマー(C)10~40質量部を溶融混練してマスターバッチ(X)を調製する工程。
工程2:芳香族ジカルボン酸単位とジオール単位とを含むポリエステル樹脂(A)80~98質量%、及びメタキシリレンジアミン単位を70モル%以上含むジアミン単位と、α,ω-脂肪族ジカルボン酸単位を70モル%以上含むジカルボン酸単位とを含むポリアミド樹脂(B)20~2質量%を含む樹脂成分100質量部に対し、工程1で得られたマスターバッチ(X)を0.055~1.1質量部を溶融混練する工程。
<3>上記<1>に記載のポリエステル系樹脂組成物からなる層を少なくとも1層有する成形体。
本発明に用いられるポリエステル樹脂(A)は、芳香族ジカルボン酸単位とジオール単位を含む。芳香族ジカルボン酸単位は、ポリエステル樹脂の結晶性、及び使用前の乾燥の容易さの観点から、テレフタル酸単位を好ましくは70モル%以上、より好ましくは80モル%以上、更に好ましくは90~100モル%含む。また、ジオール単位は、同様の観点から、炭素数2~4の脂肪族グリコール単位を好ましくは70モル%以上、より好ましくは80モル%以上、更に好ましくは90~100モル%含む。
本発明に用いられるポリアミド樹脂(B)は、ポリエステル樹脂(A)のガスバリア性を改善する効果を付与する。
ポリアミド樹脂(B)におけるジアミン単位としては、メタキシリレンジアミン単位を70モル%以上、好ましくは80モル%以上、より好ましくは90~100モル%含む。メタキシリレンジアミンをジアミン単位の主成分とすることで得られるポリアミドのガスバリア性を効率良く高めることができる。
メタキシリレンジアミン以外に使用できるジアミンとしては、パラキシリレンジアミン、1,3-ビス(アミノメチル)シクロヘキサン、1,4-ビス(アミノメチル)シクロヘキサン、テトラメチレンジアミン、ヘキサメチレンジアミン、ノナンメチレンジアミン、2-メチル-1,5-ペンタンジアミン等が例示できるが、これらに限定されるものではない。
α,ω-脂肪族ジカルボン酸としてはスベリン酸、アジピン酸、アゼライン酸、セバシン酸等が挙げられるが、アジピン酸やセバシン酸が好ましく用いられる。
α,ω-脂肪族ジカルボン酸以外のジカルボン酸単位としては、1,3-シクロヘキサンジカルボン酸や1,4-シクロヘキサンジカルボン酸等の脂環族ジカルボン酸、テレフタル酸、イソフタル酸、オルソフタル酸、キシリレンジカルボン酸、ナフタレンジカルボン酸などの芳香族ジカルボン酸等が例示できるが、これらに限定されるものではない。
なお、ここで言う相対粘度は、ポリアミド1gを96%硫酸100mLに溶解し、キャノンフェンスケ型粘度計にて25℃で測定した落下時間(t)と、同様に測定した96%硫酸そのものの落下時間(t0)との比であり、次式で示される。
相対粘度=t/t0
本発明に用いられるエポキシ官能性ポリマー(C)は、下記一般式(c1)で表されるスチレン単位及び下記一般式(c2)で表されるグリシジル(メタ)アクリレート単位を少なくとも有し、好ましくは更に下記一般式(c3)で表される(メタ)アクリレート単位を有する。
また、R6は炭素数1~12のアルキル基を表し、好ましくは炭素数1~6であり、直鎖状、分岐状又は環状であってもよい。該アルキル基の具体例としては、メチル基、エチル基、プロピル基等が挙げられ、メチル基が特に好ましい。
なかでも、前記一般式(c2)中のR4がメチル基である場合、並びに前記一般式(c3)中のR5がメチル基である場合、該エポキシ官能性ポリマーを含むポリエスエル系樹脂組成物からなる成形体は透明性に優れることから、特に好ましい。
また、前記一般式(c3)で表される(メタ)アクリレート単位を有する場合、前記一般式(c1)で表されるスチレン単位の数x、前記一般式(c2)で表されるグリシジル(メタ)アクリレート単位の数y及び前記一般式(c3)で表される(メタ)アクリレート単位の数zは、それぞれ独立に1~20であり、yは、透明性の観点から好ましくは2~20、より好ましくは3~10である。x+zは、好ましくは10より大きい。
各構成単位は任意の順序で結合でき、前記一般式(I)で表されるエポキシ官能性ポリマーは、ブロック共重合体であってもランダム共重合体であってもよい。
本発明の樹脂組成物には、本発明の効果を損なわない範囲で酸化防止剤、艶消剤、耐熱安定剤、耐候安定剤、紫外線吸収剤、核剤、可塑剤、難燃剤、帯電防止剤、着色防止剤、滑剤、ゲル化防止剤等の添加剤、層状珪酸塩等のクレイやナノフィラー等を配合することもできる。
前記ポリエステル系樹脂組成物を製造する方法は特に限定されない。例えば、ポリエステル樹脂(A)とポリアミド樹脂(B)とエポキシ官能性ポリマー(C)とを押出機内で溶融混練して所望の樹脂組成物を得ることができる。また、あらかじめポリエステル樹脂(A)又はポリアミド樹脂(B)とエポキシ官能性ポリマー(C)とを溶融混練してマスターバッチを調製し、これとポリエステル樹脂(A)とポリアミド樹脂(B)とを溶融混練してもよい。分散性の観点からは、下記工程1及び2を含む方法が好ましい。
工程1:芳香族ジカルボン酸単位とジオール単位とを含むポリエステル樹脂(A)100質量部に対してエポキシ官能性ポリマー(C)10~40質量部を溶融混練してマスターバッチ(X)を調製する工程。
工程2:芳香族ジカルボン酸単位とジオール単位とを含むポリエステル樹脂(A)80~98質量%、及びメタキシリレンジアミン単位を70モル%以上含むジアミン単位と、α,ω-脂肪族ジカルボン酸単位を70モル%以上含むジカルボン酸単位とを含むポリアミド樹脂(B)20~2質量%を含む樹脂成分100質量部に対し、工程1で得られたマスターバッチ(X)を0.055~1.1質量部を溶融混練する工程。
本発明のポリエステル系樹脂組成物は、各種包装材料、工業用材料などのガスバリア性を要求されるあらゆる用途に利用でき、フィルム、シート、薄肉中空容器等の成形体に成形できる。
本発明の成形体は、前記ポリエステル系樹脂組成物からなる層を少なくとも1層有する。本発明の成形体は、前記ポリエステル系樹脂組成物からなる単層構造であってもよく、前記ポリエステル系樹脂組成物からなる層の少なくとも一方に他の熱可塑性樹脂層(例えばポリエステル樹脂層や接着性樹脂層)を積層してもよく、前記ポリエステル系樹脂組成物層を2層以上積層した多層構造を有するものでもよい。
また、トレイやカップ等の容器は射出成形機から金型中に溶融した樹脂組成物を射出して製造する方法や、シートを真空成形や圧空成形等の成形法によって成形して得ることができる。本発明の樹脂組成物を利用してなる成形体は上述の製造方法によらず、様々な方法を経て製造することが可能である。
実施例及び比較例では以下の材料を使用した。
(1)ポリエステル樹脂(A)
以下のPET樹脂を使用した。使用に際しては、除湿乾燥機にて150℃6時間乾燥したペレットを用いた。
PET1(日本ユニペット(株)製、商品名:「RT-543C」、固有粘度=0.75dl/g、ホモPET)
PET2(日本ユニペット(株)製、商品名:「BK-2180」、固有粘度=0.83dl/g、1.5モル%イソフタル酸共重合PET)
(2)ポリアミド樹脂(B)
ポリメタキシリレンアジパミド(三菱ガス化学(株)製、商品名:「MXナイロンS6007」、数平均分子量Mn=23,000)のペレットを使用した。
(3)エポキシ官能性ポリマー(C)、マスターバッチ(X)
エポキシ官能性ポリマー(BASF社製、商品名:「Joncryl ADR-4368」、重量平均分子量6,800、エポキシ価285g/mol)を使用した。本実施例で使用したポリマーは、少なくとも前記一般式(c1)及び(c2)で表される単位をそれぞれ有し、R1~R3がそれぞれ水素原子、R4がメチル基、xが31~34、yが22~25である。使用に際しては、PET樹脂(A)100質量部に対してエポキシ官能性ポリマー(C)30質量部を溶融混練して得られる樹脂組成物(マスターバッチ(X))を、真空乾燥機にて140℃5時間乾燥したものを用いた。
実施例及び比較例で使用した材料の物性並びにポリエステル系容器の物性は、以下の方法によって分析及び測定を行った。
(1)ポリアミド樹脂の末端基濃度
(a)末端アミノ基濃度([NH2]mmol/kg)
ポリアミド樹脂0.5gを精秤し、フェノール/エタノール=4/1容量溶液30mlにポリアミドを撹拌下に溶解した。ポリアミドが完全に溶解した後、N/100塩酸で中和滴定して求めた。
(b)末端カルボキシル基濃度([COOH]mmol/kg)
ポリアミド樹脂0.5gを精秤し、ベンジルアルコール30mlに窒素気流下160~180℃でポリアミドを撹拌下に溶解した。ポリアミドが完全に溶解した後、窒素気流下80℃まで冷却し、撹拌しながらメタノール10mlを加え、N/100水酸化ナトリウム水溶液で中和滴定して求めた。
ポリアミド樹脂のアミノ基濃度([NH2]mmol/kg)及びカルボキシル基濃度([COOH]mmol/kg)から、下式により数平均分子量(Mn)を算出した。
Mn=2×106/([NH2]+[COOH])
(3)ポリエステル樹脂及びポリアミド樹脂の融点
示差走査熱量計((株)島津製作所製、商品名:「DSC-60」)を用い、窒素気流下にて昇温速度10℃/minにて測定を行い、融解ピーク温度を融点とした。
未延伸シート及び二軸延伸フィルムのヘイズは、JIS K7105に準じて、5cm×5cmに切出し、色彩・濁度同時測定器(日本電色工業(株)製、商品名:「COH-400」)を用いて測定した。
ポリエステル系容器のヘイズは、JIS K7105に準じて、ボトル胴部を5cm×5cmに切出し、上記と同様に測定した。
未延伸シート及び二軸延伸フィルムについては、酸素透過率測定装置(MOCON社製、商品名:「OX-TRAN 2/21SH」)を使用して、23℃、60%RHの条件にて0.3mmシート及び35μmフィルムの酸素透過率の測定を行った。数値が低いほど酸素の透過量が少なく好ましい。
単層ボトルについては、酸素透過率測定装置(MOCON社製、商品名:「OX-TRAN 2/21」)を使用して、容器内部湿度100%RH、外湿度50%RH、温度23℃の条件にて酸素透過率の測定を行った。数値が低いほど酸素の透過量が少なく好ましい。
タンブラーに、ポリエステル樹脂(A)のPET1の乾燥したペレットとポリアミド樹脂(B)のペレットとを、ポリエステル樹脂/ポリアミド樹脂=95/5の質量比で添加し、それらのペレット全量100質量部に対し、予め作製しておいたマスターバッチ(X)0.1質量部(エポキシ官能性ポリマー(C)として0.0231質量部)を添加した後、10分間混合した。
次いで、二軸押出機((株)プラスチック工学研究所製、スクリュー径:30mmφ、L/D=27)を用い、Tダイ法によりシリンダー温度250~275℃、Tダイ温度270℃、スクリュー回転数100rpm、冷却ロール温度75℃の条件下で成膜し、未延伸シート(幅25mm、厚さ約0.3mm)を得た。
さらに、二軸延伸機((株)東洋精機製作所製)を用いて、上記未延伸シートを100℃で1分間予備加熱した後、線延伸速度3000mm/分、縦及び横方向の延伸倍率がそれぞれ3.0倍の条件で、縦及び横方向に同時に延伸し、厚さ約35μmの二軸延伸フィルムを得た。
マスターバッチ(X)の添加量を0.2質量部(エポキシ官能性ポリマー(C)として0.0462質量部)に変更したこと以外は実施例1と同様にして未延伸シート及び二軸延伸フィルムを得た。
マスターバッチ(X)を添加しなかったこと以外は実施例1と同様にして未延伸シート及び二軸延伸フィルムを得た。
タンブラーに、ポリエステル樹脂(A)のPET1の乾燥したペレットとポリアミド樹脂(B)のペレットとを、ポリエステル樹脂/ポリアミド樹脂=95/5の質量比で添加し、それらのペレット全量100質量部に対し、マスターバッチ(X)0.1質量部(エポキシ官能性ポリマー(C)として0.0231質量部)を添加した後、10分間混合した。
次いで、射出成形機(名機製作所(株)製、型式:「M200」、4個取り)を用いて、上記の混合したペレットを下記条件により射出成形し、単層プリフォーム(全長95mm、外径22mm、肉厚3.0mm)を得た。
<単層プリフォーム成形条件>
射出シリンダー温度:260℃
金型内樹脂流路温度:260℃
金型冷却水温度 :22℃
(二軸延伸ブロー成形条件)
プリフォーム加熱温度:103℃
延伸ロッド用圧力:0.5MPa
一次ブロー圧力:0.5MPa
二次ブロー圧力:2.5MPa
一次ブロー遅延時間:0.32sec
一次ブロー時間:0.28sec
二次ブロー時間:2.0sec
ブロー排気時間:0.6sec
金型温度:30℃
マスターバッチ(X)の添加量を0.2質量部(エポキシ官能性ポリマー(C)として0.0462質量部)に変更したこと以外は実施例3と同様にして単層ボトルを得た。
マスターバッチ(X)を添加しなかったこと以外は実施例3と同様にして単層ボトルを得た。
マスターバッチ(X)の添加量を0.005質量部(エポキシ官能性ポリマー(C)として0.0012質量部)に変更したこと以外は実施例3と同様にして単層ボトルを得た。
ポリエステル樹脂(A)としてPET2を用いた以外は実施例3と同様にして単層ボトルを得た。
ポリエステル樹脂(A)としてPET2を用いた以外は実施例4と同様にして単層ボトルを得た。
ポリエステル樹脂(A)としてPET2を用いた以外は比較例2と同様にして単層ボトルを得た。
Claims (10)
- 前記ポリエステル樹脂(A)が、テレフタル酸単位を70モル%以上含む芳香族ジカルボン酸単位と、炭素数2~4の脂肪族グリコール単位を70モル%以上含むジオール単位とを含む、請求項1又は2に記載のポリエステル系樹脂組成物。
- 前記ポリエステル樹脂(A)が、芳香族ジカルボン酸単位中にスルホイソフタル酸金属塩単位を0.01~2モル%含む、請求項1~3のいずれかに記載のポリエステル系樹脂組成物。
- 前記一般式(c2)のR4が水素原子又はメチル基を表す、請求項1~4のいずれかに記載のポリエステル系樹脂組成物。
- 前記一般式(c3)中R5が水素原子又はメチル基を表す、請求項2~5のいずれかに記載のポリエステル系樹脂組成物。
- 前記一般式(c3)中のR6がメチル基を表す、請求項2~6のいずれかに記載のポリエステル系樹脂組成物。
- 下記工程1及び2を含む、請求項1~7のいずれかに記載のポリエステル系樹脂組成物の製造方法。
工程1:芳香族ジカルボン酸単位とジオール単位とを含むポリエステル樹脂(A)100質量部に対してエポキシ官能性ポリマー(C)10~40質量部を溶融混練してマスターバッチ(X)を調製する工程。
工程2:芳香族ジカルボン酸単位とジオール単位とを含むポリエステル樹脂(A)80~98質量%、及びメタキシリレンジアミン単位を70モル%以上含むジアミン単位と、α,ω-脂肪族ジカルボン酸単位を70モル%以上含むジカルボン酸単位とを含むポリアミド樹脂(B)20~2質量%を含む樹脂成分100質量部に対し、工程1で得られたマスターバッチ(X)を0.055~1.1質量部を溶融混練する工程。 - 請求項1~7のいずれかに記載のポリエステル系樹脂組成物からなる層を少なくとも1層有する成形体。
- フィルム、シート又は容器である、請求項9に記載の成形体。
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JP6013553B1 (ja) * | 2015-04-30 | 2016-10-25 | 株式会社イノアックコーポレーション | 樹脂組成物と中空成形体 |
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US10066099B2 (en) * | 2013-12-25 | 2018-09-04 | Mitsubishi Gas Chemical Company, Inc. | Polyester-based resin composition, and molded body using the resin composition |
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JPWO2017094542A1 (ja) * | 2015-12-01 | 2018-09-13 | 三菱瓦斯化学株式会社 | ポリエステル系樹脂組成物及びその製造方法、成形体及びその製造方法、並びに、マスターバッチ |
US11130859B2 (en) | 2015-12-01 | 2021-09-28 | Mitsubishi Gas Chemical Company, Inc. | Polyester-based resin composition and production process therefor, molded object and production process therefor, and masterbatch |
WO2017150109A1 (ja) * | 2016-02-29 | 2017-09-08 | 三菱瓦斯化学株式会社 | 塩素系液体漂白剤組成物用容器及び漂白剤物品 |
JPWO2017150109A1 (ja) * | 2016-02-29 | 2018-12-20 | 三菱瓦斯化学株式会社 | 塩素系液体漂白剤組成物用容器及び漂白剤物品 |
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Publication number | Publication date |
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EP2824145A4 (en) | 2015-10-21 |
CN104159970A (zh) | 2014-11-19 |
TW201343778A (zh) | 2013-11-01 |
RU2623261C2 (ru) | 2017-06-23 |
US20150030793A1 (en) | 2015-01-29 |
RU2014140749A (ru) | 2016-04-27 |
KR101991502B1 (ko) | 2019-06-20 |
CN104159970B (zh) | 2016-05-25 |
EP2824145A9 (en) | 2015-04-29 |
JP2013185138A (ja) | 2013-09-19 |
EP2824145A1 (en) | 2015-01-14 |
JP6028343B2 (ja) | 2016-11-16 |
EP2824145B1 (en) | 2018-08-29 |
KR20140135970A (ko) | 2014-11-27 |
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