WO2015115386A1 - ポリアセタール樹脂組成物および樹脂成形品 - Google Patents
ポリアセタール樹脂組成物および樹脂成形品 Download PDFInfo
- Publication number
- WO2015115386A1 WO2015115386A1 PCT/JP2015/052092 JP2015052092W WO2015115386A1 WO 2015115386 A1 WO2015115386 A1 WO 2015115386A1 JP 2015052092 W JP2015052092 W JP 2015052092W WO 2015115386 A1 WO2015115386 A1 WO 2015115386A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- polyacetal resin
- group
- compound
- carbon atoms
- mass
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/29—Compounds containing one or more carbon-to-nitrogen double bonds
- C08K5/30—Hydrazones; Semicarbazones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/22—Compounds containing nitrogen bound to another nitrogen atom
- C08K5/24—Derivatives of hydrazine
- C08K5/25—Carboxylic acid hydrazides
Definitions
- the present invention relates to a polyacetal resin composition and a resin molded product.
- Polyacetal resin has excellent mechanical properties, sliding properties, friction / abrasion properties, heat resistance, molding processability, and the like. For this reason, the polyacetal resin composition containing polyacetal resin is widely used for various machine parts, electrical parts, etc., such as a motor vehicle and OA apparatus.
- polyacetal resin uses formaldehyde as its main raw material, it undergoes a slight thermal decomposition reaction due to a thermal history during processing and the like, and generates a very small amount of formaldehyde.
- formaldehyde may cause sick house syndrome and the like, a polyacetal resin composition in which generation of formaldehyde is sufficiently suppressed is demanded.
- Patent Document 1 discloses a polyacetal resin composition in which a dihydrazone compound is blended in a predetermined ratio with a polyacetal resin. With this polyacetal resin composition, the amount of formaldehyde generated from a product is reduced and molded. It has also been proposed to suppress mold contamination during processing.
- the present invention has been made in view of the above circumstances, and is a polyacetal that can sufficiently suppress the generation of formaldehyde, can sufficiently suppress contamination of a mold during molding, and can impart excellent mechanical properties to a molded product. It aims at providing a resin composition and a resin molded product.
- the present inventors have repeatedly studied to solve the above problems. As a result, the present inventors make the end group of the dihydrazone compound a specific group that hardly causes steric hindrance, so that the reactivity between the dihydrazone compound and formaldehyde is particularly enhanced, and the generation of formaldehyde can be sufficiently suppressed. I thought that.
- the product obtained at this time is difficult to bleed out from the polyacetal resin composition, or even if bleeded out, it is difficult to adhere to the mold and the contamination of the mold during the molding process cannot be sufficiently suppressed. I thought.
- the present inventors also thought that if the dihydrazone compound is excessively added to the polyacetal resin, the mechanical properties of the molded product may be deteriorated. And the present inventors discovered that the said subject can be solved by the following invention.
- the present invention is selected from a dihydrazone compound (B1) represented by the following general formula (1) and a dihydrazone compound (B2) represented by the following general formula (2) with respect to 100 parts by mass of the polyacetal resin (A).
- R 1 represents an aliphatic hydrocarbon group having 4 to 20 carbon atoms, an alicyclic hydrocarbon group having 6 to 10 carbon atoms, or an aromatic hydrocarbon group having 6 to 10 carbon atoms.
- R 2 to R 5 each independently represents a hydrogen atom or an alkyl group having 1 or 2 carbon atoms, at least one of R 2 and R 3 represents an alkyl group having 1 or 2 carbon atoms, and among R 4 and R 5 At least one represents an alkyl group having 1 or 2 carbon atoms.
- R 8 represents an aliphatic hydrocarbon group having 4 to 20 carbon atoms, an alicyclic hydrocarbon group having 6 to 10 carbon atoms, or an aromatic hydrocarbon group having 6 to 10 carbon atoms.
- R 6 and R 7 each independently represents an alicyclic hydrocarbon group having 3 to 12 carbon atoms.
- the generation of formaldehyde can be sufficiently suppressed, contamination of the mold during molding can be sufficiently suppressed, and excellent mechanical properties can be imparted to the molded product.
- R 1 is preferably an aliphatic hydrocarbon group having 6 to 12 carbon atoms.
- the reactivity between the dihydrazone compound (B) and formaldehyde becomes higher, and the generation of formaldehyde is more effectively suppressed. Further, contamination of the mold during molding can be more sufficiently suppressed.
- R 3 and R 5 are hydrogen atoms, and R 2 and R 4 are methyl groups.
- R 3 and R 5 are preferably a hydrogen atom or a methyl group.
- the reactivity between the dihydrazone compound (B) and formaldehyde becomes higher, and the generation of formaldehyde is more effectively suppressed. Further, contamination of the mold during molding can be more sufficiently suppressed.
- the dihydrazone compound (B) is preferably blended with 100 parts by mass of the polyacetal resin (A).
- the hydrazide compound (C) is further blended at a ratio of 0.01 to 1 part by mass with respect to 100 parts by mass of the polyacetal resin (A).
- the generation of formaldehyde can be more sufficiently suppressed as compared with the case where the blending amount of the hydrazide compound (C) with respect to 100 parts by mass of the polyacetal resin (A) is less than 0.01 parts by mass.
- the compounding quantity of the hydrazide compound (C) with respect to 100 mass parts of polyacetal resin (A) exceeds 1 mass part, the contamination of the metal mold
- more excellent mechanical properties can be imparted to the molded product obtained.
- the hydrazide compound (C) is preferably composed of at least one selected from the group consisting of a monohydrazide compound and a dihydrazide compound.
- the hydrazide compound (C) is composed of a hydrazide compound having three or more hydrazide groups in the molecule, the hydrazide group can be efficiently dispersed in the polyacetal resin, and the hydrazide compound (C) The amount added can be more sufficiently suppressed.
- the hydrazide compound (C) is particularly preferably composed of a dihydrazide compound.
- the generation of formaldehyde can be more sufficiently suppressed as compared with the case where the hydrazide compound is composed of only the monohydrazide compound or the case of being composed of the monohydrazide compound and the dihydrazide compound.
- the present invention is a resin molded product obtained by molding the polyacetal resin composition.
- a polyacetal resin composition and a resin molded product that can sufficiently suppress the generation of formaldehyde, can sufficiently suppress the contamination of the mold during molding, and can impart excellent mechanical properties to the molded product. can do.
- the present invention is selected from a dihydrazone compound (B1) represented by the following general formula (1) and a dihydrazone compound (B2) represented by the following general formula (2) with respect to 100 parts by mass of the polyacetal resin (A).
- R 1 represents an aliphatic hydrocarbon group having 4 to 20 carbon atoms, an alicyclic hydrocarbon group having 6 to 10 carbon atoms, or an aromatic hydrocarbon group having 6 to 10 carbon atoms.
- R 2 to R 5 each independently represents a hydrogen atom or an alkyl group having 1 or 2 carbon atoms, at least one of R 2 and R 3 represents an alkyl group having 1 or 2 carbon atoms, and among R 4 and R 5 At least one represents an alkyl group having 1 or 2 carbon atoms.
- R 8 represents an aliphatic hydrocarbon group having 4 to 20 carbon atoms, an alicyclic hydrocarbon group having 6 to 10 carbon atoms, or an aromatic hydrocarbon group having 6 to 10 carbon atoms.
- R 6 and R 7 each independently represents an alicyclic hydrocarbon group having 3 to 12 carbon atoms.
- the polyacetal resin is not particularly limited, and even if it is a homopolymer containing only a divalent oxymethylene group as a constituent unit, the divalent oxymethylene group and 2 having 2 or more carbon atoms It may be a copolymer containing a valent oxyalkylene group as a constituent unit.
- Examples of the oxyalkylene group having 2 or more carbon atoms include an oxyethylene group, an oxypropylene group, and an oxybutylene group.
- the ratio of the oxyalkylene group having 2 or more carbon atoms to the total number of moles of the oxymethylene group and the oxyalkylene group having 2 or more carbon atoms is not particularly limited, and is 0.5 to 10 mol%, for example. If it is.
- the number of carbon atoms in the oxyalkylene group may be 2 or more, preferably 6 or less, more preferably 4 or less.
- trioxane is usually used as a main raw material.
- cyclic formal or cyclic ether can be used.
- the cyclic formal include, for example, 1,3-dioxolane, 1,3-dioxane, 1,3-dioxepane, 1,3-dioxocane, 1,3,5-trioxepane and 1,3,6-trioxocane.
- the cyclic ether include ethylene oxide, propylene oxide, butylene oxide and the like.
- 1,3-dioxolane may be used, and in order to introduce an oxypropylene group, 1,3-dioxane may be used.
- 1,3-dioxepane may be introduced.
- the amount of hemi-formal end groups, the amount of formyl end groups, the amount of end groups unstable to heat, acid, and base is small.
- the hemi-formal end group is represented by —OCH 2 OH
- the formyl end group is represented by —CHO.
- the dihydrazone compound (B) blended in the polyacetal resin composition of the present invention is a dihydrazone compound (B1) represented by the above general formula (1) and a dihydrazone represented by the above general formula (2). At least one of the compounds (B2).
- R 1 represents an aliphatic hydrocarbon group having 4 to 20 carbon atoms, an alicyclic hydrocarbon group having 6 to 10 carbon atoms, or an aromatic hydrocarbon group having 6 to 10 carbon atoms.
- the aliphatic hydrocarbon group may be saturated or unsaturated, and may be linear or branched.
- aliphatic hydrocarbon group examples include a butylene group, a pentylene group, a hexylene group, a heptylene group, an octylene group, a nonylene group, a decylene group, an undecylene group, a dodecylene group, a tridecylene group, a tetradecylene group, a pentadecylene group, and a hexadecylene group.
- Groups, alkylene groups such as heptadecylene group, octadecylene group, nonadecylene group and icosylene group.
- the aliphatic hydrocarbon group is preferably an aliphatic hydrocarbon group having 6 to 12 carbon atoms.
- the reactivity between the dihydrazone compound (B) and formaldehyde becomes higher, and generation of formaldehyde is more effectively suppressed. Further, contamination of the mold during molding can be more sufficiently suppressed.
- the alicyclic hydrocarbon group may be saturated or unsaturated.
- Examples of the alicyclic hydrocarbon group include a cycloalkylene group having 6 to 10 carbon atoms.
- Examples of the cycloalkylene group include a cyclohexylene group.
- aromatic hydrocarbon group examples include arylene groups such as a phenylene group and a naphthylene group.
- a substituent may be bonded to at least a part of the carbon atoms of the aromatic hydrocarbon group.
- substituents include a halogen group, a nitro group, and an alkyl group having 1 to 20 carbon atoms.
- R 2 to R 5 each independently represent a hydrogen atom or an alkyl group having 1 or 2 carbon atoms, and at least one of R 2 and R 3 is an alkyl group having 1 or 2 carbon atoms. And at least one of R 4 and R 5 represents an alkyl group having 1 or 2 carbon atoms.
- R 3 and R 5 are hydrogen atoms
- R 2 and R 4 are methyl groups
- 3 and R 5 are preferably a hydrogen atom or a methyl group.
- the reactivity between the dihydrazone compound (B) and formaldehyde becomes higher, and the generation of formaldehyde is more effectively suppressed. Further, contamination of the mold during molding can be more sufficiently suppressed.
- alkyl group having 1 or 2 carbon atoms examples include a methyl group and an ethyl group.
- dihydrazone compound (B1) represented by the general formula (1) examples include, for example, 1,12-bis [2- (1-methylethylidene) hydrazino]]-1,12-dodecanedione, 1,12 -Bis (2-ethylidenehydrazino) -1,12-dodecanedione, 1,12-bis (2-propylidenehydrazino) -1,12-dodecanedione, 1,12-bis [2- (1-methyl Propylidene) hydrazino] -1,12-dodecanedione, 1,12-bis [2- (1-ethylpropylidene) hydrazino] -1,12-dodecanedione, 1,10-bis [2- (1-methyl) Ethylidene) hydrazino]]-1,10-decanedione, 1,10-bis (2-propylidenehydrazino) -1,10-decanedione
- the dihydrazone compound (B1) represented by the general formula (1) may be used alone or in combination of two or more.
- R 8 is an aliphatic hydrocarbon group having 4 to 20 carbon atoms, an alicyclic hydrocarbon group having 6 to 10 carbon atoms, or an aromatic group having 6 to 10 carbon atoms in the same manner as R 1.
- a hydrocarbon group is shown.
- R 8 may be the same as or different from R 1 in the general formula (1).
- R 6 and R 7 each independently represents an alicyclic hydrocarbon group having 3 to 12 carbon atoms.
- Examples of the alicyclic hydrocarbon group having 3 to 12 carbon atoms include a cyclohexylene group.
- dihydrazone compound (B2) represented by the above general formula (2) include, for example, 1,12-bis (2-cyclohexylidenehydrazino) -1,12-dodecanedione, 1,10-bis ( And 2-cyclohexylidenehydrazino) -1,10-decanedione and 1,6-bis (2-cyclohexylidenehydrazino) -1,6-hexanedione.
- the dihydrazone compound (B2) represented by the general formula (2) may be used alone or in combination of two or more.
- the compounding quantity of a dihydrazone compound (B) is 0.02 mass part or more with respect to 100 mass parts of polyacetal resin.
- the blending amount of the dihydrazone compound (B) with respect to 100 parts by mass of the polyacetal resin is preferably 0.05 parts by mass or more, more preferably 0.1 parts by mass or more, from the viewpoint of further suppressing generation of formaldehyde. Especially preferably, it is 0.3 mass part or more.
- the compounding quantity of the dihydrazone compound (B) with respect to 100 mass parts of polyacetal resin is 5 mass parts or less. If the blending amount of the dihydrazone compound (B) exceeds 5 parts by mass, excellent mechanical properties cannot be imparted to the molded product.
- the blending amount of the dihydrazone compound (B) with respect to 100 parts by mass of the polyacetal resin is preferably 3 parts by mass or less from the viewpoint of further improving the mechanical properties of the molded product obtained by molding the polyacetal resin composition. Furthermore, it is preferable that the compounding quantity of the dihydrazone compound (B) with respect to 100 mass parts of polyacetal resins is 0.5 mass part or less from a viewpoint of suppressing mold contamination more.
- the blending amount of the dihydrazone compound (B) is preferably 0.05 to 3 parts by mass with respect to 100 parts by mass of the polyacetal resin.
- production of formaldehyde can be suppressed more fully.
- the compounding quantity of a dihydrazone compound (B) exceeds 3 mass parts, the more excellent mechanical characteristic can be provided with respect to the molded article obtained by shape
- the blending amount of the dihydrazone compound (B) is more preferably 0.1 to 1.0 part by mass with respect to 100 parts by mass of the polyacetal resin.
- the dihydrazone compound (B1) and the dihydrazone compound (B2) are produced by reacting a dicarboxylic acid derivative such as a dicarboxylic acid halide or dicarboxylic acid ester with hydrazine to produce a dihydrazide compound, and reacting the dihydrazide compound with a ketone or an aldehyde. Can be obtained.
- R 1 (COX) 2 or R 8 (COX) 2 is used as the dicarboxylic acid halide
- R 1 (COOY) 2 or R 8 (COOY) 2 is used as the dicarboxylic acid ester.
- Y represents an alkyl group.
- R 2 —C ( ⁇ O) —R 3 , R 4 —C ( ⁇ O) —R 5 , R 6 ⁇ O, or R 7 ⁇ O is used as the ketone or aldehyde.
- the polyacetal resin composition of the present invention may contain at least one of a hydrazide compound (C), a heat stabilizer (D), a release agent (E), and a weather stabilizer (F) as necessary. Good.
- a hydrazide compound (C), a heat stabilizer (D), a release agent (E), and a weather stabilizer (F) as necessary.
- the hydrazide compound (C), the heat stabilizer (D), the mold release agent (E), and the weather resistance stabilizer (F) will be described in detail.
- the hydrazide compound (C) may be any hydrazide compound having at least one hydrazide group in the molecule.
- Examples of the hydrazide compound (C) include polyhydrazide compounds such as monohydrazide compounds, dihydrazide compounds, and trihydrazide compounds.
- a hydrazide compound having three or more hydrazide groups in the molecule is referred to as a polyhydrazide compound.
- the monohydrazide compound either an aliphatic monohydrazide compound or an aromatic monohydrazide compound can be used.
- Examples of the aliphatic monohydrazide compound include propionic acid hydrazide, thiocarbohydrazide, and stearic acid hydrazide.
- aromatic monohydrazide compound examples include salicylic acid hydrazide, 3-hydroxy-2-naphthoic acid hydrazide, p-toluenesulfonyl hydrazide, aminobenzhydrazide and 4-pyridinecarboxylic acid hydrazide.
- the dihydrazide compound can be either an aliphatic monohydrazide compound or an aromatic monohydrazide compound.
- Examples of the aliphatic dihydrazide compound include carbodihydrazide, oxalic acid dihydrazide, malonic acid dihydrazide, succinic acid dihydrazide, glutaric acid dihydrazide, adipic acid dihydrazide, azelaic acid dihydrazide, sebacic acid dihydrazide 1, dodecanedioic acid dihydrazide 1, Hydrazide), 1,18-octadecandicarbohydrazide, stearic acid dihydrazide, maleic acid dihydrazide, fumaric acid dihydrazide, 7,11-octadecadiene-1,18-dicarbohydrazide and the like.
- aromatic dihydrazide compounds include isophthalic acid dihydrazide, terephthalic acid dihydrazide, 1,5-naphthalenedicarbohydrazide, 1,8-naphthalenedicarbohydrazide, 2,6-naphthalenedicarbohydrazide, 4,4′-oxybis. Examples thereof include benzenesulfonyl hydrazide and 1,5-diphenylcarbonohydrazide.
- polyhydrazide compound examples include aminopolyacrylamide and 1,3,5-tris (2-hydrazinocarbonylethyl) isocyanurate.
- the hydrazide compound (C) may be used alone or in combination of two or more.
- the blending amount of the hydrazide compound (C) with respect to 100 parts by mass of the polyacetal resin (A) is preferably 0.01 to 1 part by mass.
- the generation of formaldehyde can be more sufficiently suppressed as compared with the case where the blending amount of the hydrazide compound (C) with respect to 100 parts by mass of the polyacetal resin (A) is less than 0.01 parts by mass.
- the compounding quantity of the hydrazide compound (C) with respect to 100 mass parts of polyacetal resin (A) exceeds 1 mass part, the contamination of the metal mold
- more excellent mechanical properties can be imparted to the molded product obtained.
- the hydrazide compound (C) is preferably composed of at least one selected from the group consisting of a monohydrazide compound and a dihydrazide compound.
- the hydrazide compound (C) is composed of a hydrazide compound having three or more hydrazide groups in the molecule, the hydrazide group can be efficiently dispersed in the polyacetal resin, and the hydrazide compound (C) The amount added can be more sufficiently suppressed.
- the hydrazide compound (C) is preferably composed of a dihydrazide compound.
- generation of formaldehyde can be more sufficiently suppressed as compared with the case where the hydrazide compound is composed of only the monohydrazide compound or the case of being composed of the monohydrazide compound and the dihydrazide compound.
- the blending amount of the hydrazide compound (C) with respect to 100 parts by mass of the polyacetal resin (A) is preferably 0.3 to 1 part by mass. In this case, compared with the case where the compounding quantity of the hydrazide compound (C) with respect to 100 mass parts of polyacetal resin (A) is less than 0.3 mass part, generation
- a heat stabilizer is not specifically limited, As a heat stabilizer, a hindered phenol compound or a triazine compound is used preferably. These may be blended singly or in combination of two or more. In this case, the generation of formaldehyde is further effectively suppressed.
- the hindered phenol (sterically hindered phenol) compound is a compound having a structure represented by the following general formula (3) and having at least one structure in the molecule having a substituent at the ortho position relative to the phenolic hydroxyl group.
- R 9 and R 10 each independently represent a substituted or unsubstituted alkyl group.
- Examples of the alkyl group represented by R 9 and R 10 include those having 1 to 6 carbon atoms such as methyl, ethyl, propyl, butyl, and amyl groups. Among them, a bulky branched alkyl group such as a t-butyl group is preferable, and at least one of R 9 and R 10 is preferably such a branched alkyl group.
- a group in which a hydrogen atom of an unsubstituted alkyl group is substituted with a halogen atom such as chlorine can be used.
- hindered phenol compound used in the present invention examples include 2,2′-methylene-bis (4-methyl-6-tert-butylphenol) and 4,4′-methylene-bis (2,6-di-tert-butylphenol). ), 1,3,5-trimethyl-2,4,6-tris (3,5-di-tert-butyl-4-hydroxybenzyl) benzene, 3,5-di-tert-butyl-4-hydroxybenzyldimethyl Amine, distearyl-3,5-di-t-butyl-4-hydroxybenzylphosphonate, diethyl-3,5-di-t-butyl-4-hydroxybenzylphosphonate, 2,6,7-trioxa-1-phospha -Bicyclo [2,2,2] -oct-4-yl-methyl-3,5-di-t-butyl-4-hydroxyhydrocinnamate, 3,5-di-t-butyl-4- Droxyphenyl-3,5-dist
- R 9 and R 10 each have the same meanings as R 9 and R 10 in the general formula (3).
- 1,6-hexanediol-bis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate], pentaerythritol-tetrakis [3- (3,5-di-t-butyl- 4-hydroxyphenyl) propionate], triethylene glycol-bis [3- (3,5-dimethyl-4-hydroxyphenyl) propionate], triethylene glycol-bis [3- (3-t-butyl-5-methyl- 4-hydroxyphenyl) propionate], triethylene glycol-bis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate], 2,2′-thiodiethyl-bis [3- (3,5 -Di-t-butyl-4-hydroxyphenyl) propionate], etc.
- An ester of propionic acid having a droxyphenyl group and a polyhydric alcohol is also preferred.
- the triazine compound is basically an amino-substituted triazine compound having a structure represented by the following general formula (5), or an initial polycondensate of the amino-substituted triazine compound and formaldehyde.
- R 11 , R 12 and R 13 are each independently a hydrogen atom, halogen atom, hydroxyl group, mercapto group, alkyl group, aralkyl group, aryl group, cycloalkyl group, amino group or A substituted amino group, at least one of which represents an amino group or a substituted amino group.
- amino-substituted triazine compound or the initial polycondensate of amine-substituted triazine compound and formaldehyde include, for example, guanamine, melamine, N-butylmelamine, N-phenylmelamine, N, N-diphenylmelamine, N, N -Diallylmelamine, N, N ', N "-triphenylmelamine, N, N', N" -trimethylolmelamine, benzoguanamine, 2,4-diamino-6-methyl-sym-triazine, 2,4-diamino- 6-butyl-sym-triazine, 2,4-diamino-6-benzyloxy-sym-triazine, 2,4-diamino-6-butoxy-sym-triazine, 2,4-diamino-6-cyclohexyl-sym-triazine 2,4-di
- the blending amount of the heat stabilizer (D) is preferably 0.01 to 3 parts by weight, more preferably 0.05 to 2 parts by weight, and more preferably 0.1 to 1 part per 100 parts by weight of the polyacetal resin. More preferably, it is part by mass.
- the thermal decomposition of the polyacetal resin is less than when the blending amount of the heat stabilizer (D) is less than 0.01 parts by mass. It is more effectively suppressed and the generation of formaldehyde is more effectively suppressed.
- the mechanical characteristic of a polyacetal resin composition can be improved more.
- release agent Although a release agent is not specifically limited, as a release agent, polyethylene, silicone oil, a fatty acid, fatty acid ester, or a fatty acid metal salt is used preferably. These may be blended singly or in combination of two or more. In this case, contamination of the mold during the molding process is further effectively suppressed.
- polyethylene waxes such as low molecular weight polyethylene or low molecular weight polyethylene copolymers, and modified polyethylene waxes in which polar groups are introduced by oxidative modification or acid modification thereof.
- the number average molecular weight of polyethylene is preferably 500 to 15000, more preferably 1000 to 10,000.
- Polyethylene wax such as low molecular weight polyethylene and low molecular weight polyethylene copolymer is a method of directly polymerizing ethylene or ethylene and ⁇ -olefin using a Ziegler catalyst, a method of obtaining high molecular weight polyethylene or a by-product during the production of the copolymer Further, it can be produced by a method of thermally decomposing a high molecular weight polyethylene or copolymer.
- a polyethylene wax is preferably a copolymer type polyethylene wax of 50 to 99 mol% of ethylene and 1 to 50 mol% of an ⁇ -olefin, and a particularly preferable polyethylene wax is a polyethylene wax in which the ⁇ -olefin is propylene.
- Oxidation-modified polyethylene wax is obtained by treating polyethylene wax with peroxide or oxygen to introduce polar groups such as carboxyl groups and hydroxyl groups.
- Acid-modified polyethylene wax is introduced with polar groups such as carboxyl groups and sulfonic acid groups by treatment with inorganic acids, organic acids or unsaturated carboxylic acids in the presence of peroxide or oxygen if necessary. It is.
- These polyethylene waxes are commercially available under the names of general type high density polyethylene wax, general type low density polyethylene wax, low oxidation type polyethylene wax, high oxidation type polyethylene wax, acid-modified type polyethylene wax or special monomer modified type. And can be easily obtained.
- silicone oil examples include silicone oil made of polydimethylsiloxane, silicone oil in which a part of methyl group of polydimethylsiloxane is substituted with phenyl group, part of methyl group of polydimethylsiloxane is hydrogen or 2 or more carbon atoms Silicone oil substituted with alkyl group, silicone oil with polydimethylsiloxane partially substituted with halogenated phenyl group, silicone oil with polydimethylsiloxane partially substituted with fluoroester group Epoxy-modified silicone oils such as polydimethylsiloxane having an epoxy group, amino-modified silicone oils such as polydimethylsiloxane having an amino group, and alkylaralkyl resins such as dimethylsiloxane and phenylmethylsiloxane.
- Corn oil polyether-modified silicone oil such as polydimethylsiloxane having a structure in which a part of methyl group of dimethylsiloxane unit is substituted with polyether, a part of methyl group of dimethylsiloxane unit is substituted with polyether
- examples thereof include alkylaralkyl polyether-modified silicone oils such as polymers of dimethylsiloxane and phenylmethylsiloxane.
- Examples of the fatty acid include saturated or unsaturated fatty acids having 12 or more carbon atoms.
- Examples of fatty acids are lauric acid, tridecylic acid, myristic acid, pentadecylic acid, palmitic acid, heptadecylic acid, stearic acid, nonadecanoic acid, arachidic acid, behenic acid, lignoceric acid, serotic acid, heptacosanoic acid, montanic acid, melicic acid , Laccelic acid, oleic acid, elaidic acid, linoleic acid, linolenic acid, arachidonic acid, cetreic acid, erucic acid and the like.
- the fatty acid is preferably a saturated fatty acid having 12 to 22 carbon atoms.
- fatty acid esters include fatty acid esters of fatty acids having 5 to 32 carbon atoms and monovalent or polyhydric alcohols having 2 to 30 carbon atoms.
- fatty acids caproic acid, caprylic acid, undecylic acid, lauric acid, tridecylic acid, myristic acid, palmitic acid, stearic acid, behenic acid, lignoceric acid, serotic acid, montanic acid, melicic acid and other saturated fatty acids, or oleic acid
- unsaturated fatty acids such as elaidic acid, linoleic acid, linolenic acid, arachidonic acid, pladicic acid, erucic acid, ricinoleic acid and the like.
- Alcohols include monohydric alcohols such as propyl alcohol, isopropyl alcohol, butyl alcohol, octyl alcohol, capryl alcohol, lauryl alcohol, myristyl alcohol, stearyl alcohol, and behenyl alcohol, or ethylene glycol, propylene glycol, butanediol, glycerin, pentaerythritol. And polyhydric alcohols such as sorbitan.
- the fatty acid ester is preferably a fatty acid ester of a fatty acid having 12 to 22 carbon atoms and a monovalent or polyhydric alcohol having 2 to 22 carbon atoms.
- Fatty acid metal salt is a salt of higher fatty acid and metal.
- a higher fatty acid refers to a fatty acid having 12 or more carbon atoms. Examples of the higher fatty acid include stearic acid, oleic acid, octanoic acid, lauric acid, behenic acid, ricinoleic acid and the like. Examples of the metal include zinc, calcium, magnesium, nickel, copper and the like.
- the compounding amount of the release agent (E) is preferably 0.01 to 3 parts by mass, more preferably 0.05 to 2.5 parts by mass with respect to 100 parts by mass of the polyacetal resin. More preferably, it is ⁇ 2 parts by mass.
- the compounding amount of the release agent (E) is 0.01 to 3 parts by mass with respect to 100 parts by mass of the polyacetal resin, compared to when the compounding amount of the mold release agent (E) is less than 0.01 parts by mass.
- contamination of the mold during the molding process is more effectively suppressed.
- the mechanical characteristic of a polyacetal resin composition can be improved more.
- an anti-smudge stabilizer is further blended in the polyacetal resin composition of the present invention. In this case, generation of formaldehyde can be more effectively suppressed.
- a light stabilizer or an ultraviolet absorber is preferably used.
- a hindered amine light stabilizer is preferably used.
- those represented by the following general formula (6) are particularly preferably used.
- R 14 represents an organic group in which the bond to the nitrogen atom is a carbon atom
- X represents an organic group bonded to the 4-position of the piperidyl group via an oxygen atom or nitrogen atom, or a hydrogen atom.
- R 14 examples include linear or branched alkyl groups having 1 to 10 carbon atoms.
- alkyl group examples include a methyl group, an ethyl group, a propyl group, a t-butyl group, a hexyl group, an octyl group, and a decyl group. Of these, a methyl group is preferred.
- preferred hindered amine light stabilizers include, for example, bis (1,2,2,6,6-pentamethyl-4-piperidinyl) sebacate, 1- [2- ⁇ 3- (3,5-di-t- Butyl-4-hydroxyphenyl) propionyloxy ⁇ ethyl] -4- [3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionyloxy] -2,2,6,6-tetramethylpiperidine, Tetrakis (1,2,2,6,6-pentamethyl-4-piperidyl) -1,2,3,4-butanetetracarboxylate, 1,2,2,6,6-pentamethyl-4-piperidyl and tridecyl- 1,2,3,4-butanetetracarboxylate (part of the four ester moieties of butanetetracarboxylate is 1,2,2,6,6-pentamethyl-4-piperidi A mixture of compounds in which the others are tridecyl groups),
- the anti-stabilizing agent (F) may be blended singly or in combination of two or more.
- the blending amount of the anti-wrinkle stabilizer (F) is preferably 0.01 to 3 parts by mass, more preferably 0.03 to 2 parts by mass, and more preferably 0.05 to 1 with respect to 100 parts by mass of the polyacetal resin. More preferably, it is part by mass.
- the blending amount of the anti-wrinkle stabilizer (F) is 0.01 to 3 parts by mass, the generation of formaldehyde can be suppressed more effectively than when the blending amount is out of the above range.
- the polyacetal resin composition includes inorganic fillers, antioxidants, colorants, nucleating agents, plasticizers, optical brighteners, sliding agents, polyethylene glycol, and glycerin.
- inorganic fillers such as higher fatty acid salts may be further blended.
- an inorganic filler is mix
- any inorganic filler generally blended in a thermoplastic resin can be used.
- the inorganic filler may have any shape such as a fiber shape, a plate shape, a needle shape, a spherical shape, and a powder.
- examples of inorganic fillers include silica fibers, silica / alumina fibers, alumina fibers, zirconia fibers, boron nitride fibers, silicon nitride fibers, carbon fibers, boron fibers, potassium titanate fibers, metal fibers such as stainless steel, and fibers such as aramid fibers.
- Reinforcing filler carbon black, graphite, silica, quartz powder, glass beads, milled fiber, glass balloon, glass powder, calcium silicate, aluminum silicate, kaolin, clay, diatomaceous earth, silicates such as wollastonite, Metal oxide such as iron oxide, titanium oxide, zinc oxide, antimony trioxide, alumina, metal carbonate such as calcium carbonate, sulfate such as barium sulfate, ferrite, silicon carbide, silicon nitride, boron nitride, various metal powders, etc. Powdered inorganic fillers; mica, talc, glass flakes, etc. Jo fillers, and the like can be exemplified, may be used in combination few with these alone.
- glass fiber it is preferable to use glass fiber, carbon fiber, talc or mica.
- glass fiber from the viewpoint of mechanical properties and heat resistance.
- the inorganic filler may be used after surface treatment with a surface treatment agent such as a silane coupling agent, a titanate compound or an isocyanate compound, if necessary. Good.
- the adhesion amount is preferably 0.01 parts by mass or more and more preferably 0.05 parts by mass or more with respect to 100 parts by mass of the inorganic filler.
- thermoplastic polyurethane in order to impart toughness and impact resistance.
- a thermoplastic polyurethane a thermoplastic polyurethane having a residual isocyanate amount of 0.10% by mass or less, a water content of 3000 ppm by mass or less, and having a melt viscosity of 200,000 poise or more at 180 ° C. Is preferably used.
- the polyacetal resin composition includes a dicarboxylic acid represented by R 1 (COH) 2 , a dicarboxylic acid halide represented by R 1 (COX) 2 or R 8 (COX) 2 , R 1 (COOY) 2 or R 8 (COOY) 2 or a dicarboxylic acid ester represented by R 2 —C ( ⁇ O) —R 3 , R 4 —C ( ⁇ O) —R 5 , R 6 ⁇ O, R 7 ⁇ O, or ,
- a reaction product obtained by reacting only one end of a dihydrazide compound with R 2 —C ( ⁇ O) —R 3 , R 4 —C ( ⁇ O) —R 5 , R 6 ⁇ O, R 7 ⁇ O May further be included.
- the present invention is a resin molded product obtained by molding the polyacetal resin composition described above.
- the molding method is not particularly limited, and an injection molding method, an extrusion molding method, or the like is used as the molding method.
- the generation of formaldehyde is sufficiently suppressed. Therefore, as a countermeasure against so-called sick house syndrome, automobile interior parts, interior parts such as houses (hot water mixing plugs, etc.), clothing parts (fasteners) , Belt buckles, etc.), building material applications (piping, pump parts, etc.), and machine parts (gears, etc.).
- A Polyacetal resin (POM) An acetal copolymer obtained by copolymerizing trioxane and 1,3-dioxolane so that the content of 1,3-dioxolane in POM is 4.2% by mass, and having a melt index (ASTM-D1238) Standard: 190 ° C., 2.16 kg) is 10.5 g / 10 min.
- a glass reactor was charged with 310.0 g (1.2 mol) of dodecanedioic acid dihydrazide and 845.9 g of methanol and heated to 50 ° C. Acetone 348.5g (6.0mol) was dripped there and it reacted. After cooling, crystals were precipitated, filtered, washed with water and dried to obtain 305.0 g of B-1 (weight yield 75.1%).
- B-6 was obtained in the same manner as B-1, except that propyl aldehyde was used instead of acetone as a raw material.
- B-2 to B-5 and B-7 to B-21 were obtained in the same manner as B-1, except that acetone and dodecanedioic acid dihydrazide as raw materials were appropriately changed.
- Mold contamination suppression effect The mold contamination suppression effect was evaluated as follows. First, pellets of the polyacetal resin compositions obtained in Examples 1 to 34 and Comparative Examples 1 to 11 were molded using a so-called drop mold using a mini mat M8 / 7A molding machine manufactured by Sumitomo Heavy Industries, Ltd. 3000 shots were continuously formed at a temperature of 200 ° C. and a mold temperature of 80 ° C. After the molding, the state of the inner wall surface of the mold was observed with the naked eye.
- the standard regarding the mold contamination suppression effect was as follows. A: There is no mold deposits, and the effect of suppressing mold contamination is very good. B: Almost no mold deposits, and the effect of suppressing mold contamination is very good. C: Mold contamination with little mold deposits. Good suppression effect D: Many mold deposits, poor mold contamination suppression effect Here, A to C were accepted and D was rejected. The results are shown in Tables 1-10.
- the polyacetal resin composition of the present invention it has been confirmed that generation of formaldehyde can be sufficiently suppressed, contamination of the mold during molding can be sufficiently suppressed, and excellent mechanical properties can be imparted to the molded product. It was.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
ポリアセタール樹脂は特に限定されるものではなく、2価のオキシメチレン基のみを構成単位として含むホモポリマーであっても、2価のオキシメチレン基と、炭素数が2以上の2価のオキシアルキレン基とを構成単位として含むコポリマーであってもよい。
本発明のポリアセタール樹脂組成物に配合されるジヒドラゾン化合物(B)は、上記一般式(1)で表されるジヒドラゾン化合物(B1)及び上記一般式(2)で表されるジヒドラゾン化合物(B2)のうちの少なくとも1種である。
ヒドラジド化合物(C)は、少なくとも1個のヒドラジド基を分子内に有するヒドラジド化合物であればよい。ヒドラジド化合物(C)としては、例えばモノヒドラジド化合物、ジヒドラジド化合物、及び、トリヒドラジド化合物等のポリヒドラジド化合物が挙げられる。なお、本明細書においては、ヒドラジド基を分子内に3個以上有するヒドラジド化合物をポリヒドラジド化合物と呼ぶこととする。
熱安定剤は特に限定されるものではないが、熱安定剤としては、ヒンダードフェノール化合物又はトリアジン化合物が好ましく用いられる。これらは1種類単独で配合しても、2種類以上を組み合わせて配合してもよい。この場合、ホルムアルデヒドの発生がさらに効果的に抑制される。
離型剤は特に限定されるものではないが、離型剤としては、ポリエチレン、シリコーンオイル、脂肪酸、脂肪酸エステル又は脂肪酸金属塩が好ましく用いられる。これらは1種類単独で配合しても、2種類以上を組み合わせて配合してもよい。この場合、成形加工時の金型の汚染がさらに効果的に抑制される。
本発明のポリアセタール樹脂組成物には、さらに耐侯安定剤が配合されることが好ましい。この場合、ホルムアルデヒドの発生をより効果的に抑制できる。耐侯安定剤としては、光安定剤又は紫外線吸収剤が好ましく用いられる。光安定剤としては、ヒンダードアミン系光安定剤が好ましく用いられる。光安定剤としては、特に下記一般式(6)で表されるものが好ましく用いられる。
トリオキサンと1,3-ジオキソランとを、POM中の1,3-ジオキソランの含有率が4.2質量%となるように共重合して得られたアセタールコポリマーであって、メルトインデックス(ASTM-D1238規格:190℃、2.16kg)が10.5g/10分であるアセタールコポリマー
B-1:1,12-ビス[2-(1-メチルエチリデン)ヒドラジノ]]-1,12-ドデカンジオン
B-2:1,12-ビス[2-(1-メチルプロピリデン)ヒドラジノ]-1,12-ドデカンジオン
B-3:1,12-ビス[2-(1-エチルプロピリデン)ヒドラジノ]-1,12-ドデカンジオン
B-4:1,12-ビス(2-シクロヘキシリデンヒドラジノ)-1,12-ドデカンジオン
B-5:1,12-ビス(2-エチリデンヒドラジノ)-1,12-ドデカンジオン
B-6:1,12-ビス(2-プロピリデンヒドラジノ)-1,12-ドデカンジオン
B-7:1,8-ビス[2-(1-メチルエチリデン)ヒドラジノ]-1,8-オクタンジオン
B-8:1,6-ビス[2-(1-メチルエチリデン)ヒドラジノ]-1,6-ヘキサンジオン
B-9:1,6-ビス[2-(1-メチルプロピリデン)ヒドラジノ]-1,6-ヘキサンジオン
B-10:1,3-ビス[2-(1-メチルエチリデン)ヒドラジノカルボニル]ベンゼン
B-11:1,18-ビス[2-(1-メチルエチリデン)ヒドラジノ)-1,18-オクタデカンジオン
B-12:1,4-ビス[2-(1-メチルエチリデン)ヒドラジノ)-1,4-シクロヘキサンジオン
B-13:1,12-ビス(2-メチリデンヒドラジノ)-1,12-ドデカンジオン
B-14:1,3-ビス(2-メチリデンヒドラジノカルボニル)ベンゼン
B-15:1,12-ビス[2-(1,3-ジメチルブチリデン)ヒドラジノ]-1,12-ドデカンジオン
B-16:1,12-ビス[2-(ジフェニルメチリデン)ヒドラジノ]-1,12-ドデカンジオン
B-17:1,12-ビス(2-ベンジリデンヒドラジノ)-1,12-ドデカンジオン
B-18:1,12-ビス(2-ネオペンチリデンヒドラジノ)-1,12-ドデカンジオン
B-19:1,6-ビス[2-(1,3-ジメチルブチリデン)ヒドラジノ]-1,6-ヘキサンジオン
B-20:1,4-ビス[2-(1-メチルエチリデン)ヒドラジノ)-1,4-ブタンジオン
B-21:1,22-ビス[2-(1-メチルエチリデン)ヒドラジノ)-1,22-ドコサンジオン
C-1:1,12-ドデカン二酸ジヒドラジド
C-2:アジピン酸ジヒドラジド
C-3:イソフタル酸ジヒドラジド
C-4:ステアリン酸ヒドラジド
(実施例1~34及び比較例1~11)
ポリアセタール樹脂(A)、ジヒドラゾン化合物(B)及びヒドラジド化合物(C)を表1~10に示す配合割合で、川田製作所社製スーパーミキサーを用いて均一に混合したのち、常法に従って2軸押出機(池貝鉄工社製PCM-30、スクリュー径30mm)を用いて、スクリュー回転数120rpm、シリンダー設定温度190℃の条件下で溶融混練したのち、ストランドに押出し、ペレタイザーにてカットすることでポリアセタール樹脂組成物のペレットを製造した。なお、表1~10において、配合量の単位は質量部である。
(1)ホルムアルデヒド発生の抑制効果
ホルムアルデヒド発生の抑制効果については、ホルムアルデヒド発生量を測定し、そのホルムアルデヒド発生量に基づいて評価した。ホルムアルデヒド発生量については以下にようにして求めた。
<平板試験片の作製>
まず日精樹脂工業社製射出成形機PS-40を用い、シリンダー温度215℃、金型温度80℃にて、実施例1~34及び比較例1~11で得られたポリアセタール樹脂組成物のペレットを射出成形し、100mm×40mm×2mmの平板試験片を作製した。
<ホルムアルデヒド発生量の測定>
この平板試験片を作製した日の翌日に、この平板試験片につき、ドイツ自動車工業組合規格VDA275(自動車室内部品-改訂フラスコ法によるホルムアルデヒド放出量の定量)に記載された方法に準拠して、下記の方法によりホルムアルデヒド発生量(μg/g-POM)を測定した。
(i)まずポリエチレン容器中に蒸留水50mlを入れ、上記平板試験片を空中に吊るした状態で蓋を閉め、密閉状態で60℃にて3時間加熱した。
(ii)続いて室温で60分間放置した後、平板試験片を取り出した。
(iii)ポリエチレン容器内の蒸留水中に吸収されたホルムアルデヒド量を、UVスペクトロメーターにより、アセチルアセトン比色法で測定し、このホルムアルデヒド量を平板試験片中のPOMの質量で除した値をホルムアルデヒド発生量とした。結果を表1~10に示す。
なお、表1~10において、ホルムアルデヒド発生抑制効果に関する合否の基準は下記の通りとした。
ホルムアルデヒド発生量が2.5μg/g-POM以下 :合格
ホルムアルデヒド発生量が2.5μg/g-POM超 :不合格
金型汚染抑制効果については以下のようにして評価した。まず住友重機械工業社製ミニマットM8/7A成形機を用い、いわゆるしずく型金型を用いて、実施例1~34及び比較例1~11で得られたポリアセタール樹脂組成物のペレットを、成形温度200℃、金型温度80℃で3000ショット連続成形した。成形終了後、金型の内壁面の状態を肉眼で観察した。ここで、金型汚染抑制効果に関する基準は以下の通りとした。
A:金型付着物が全くなく、金型汚染抑制効果は極めて良好
B:金型付着物が殆ど少なく、金型汚染抑制効果は極めて良好
C:金型付着物が少しあるものの、金型汚染抑制効果は良好
D:金型付着物が多く、金型汚染抑制効果は不良
ここで、A~Cについては合格とし、Dについては不合格とした。結果を表1~10に示す。
機械特性については以下のようにして評価した。まず射出成形機(製品名:EC100S、東芝機械社製)を用い、上流から下流側に向かって配置される4つのシリンダーの各温度を、190℃、190℃、180℃、170℃に設定し、金型温度を90℃に設定して、実施例1~34及び比較例1~11で得られたポリアセタール樹脂組成物のペレットを射出成形し、ISO9988-2規格に規定される引張試験用試験片を作製した。そして、引張試験機(製品名:ストログラフAPII、東洋精機製作所社製)を用いて、ISO527規格に準拠した条件で、上記の引張試験用試験片について引張試験を行い、引張降伏強度を測定した。結果を表1~10に示す。表1~10において、機械特性の合否基準は以下の通りとした。
引張降伏強度が60MPa以上:合格
引張降伏強度が60MPa未満:不合格
Claims (8)
- ポリアセタール樹脂(A)100質量部に対して、下記一般式(1)で表されるジヒドラゾン化合物(B1)及び下記一般式(2)で表されるジヒドラゾン化合物(B2)から選ばれる群より選択される少なくとも1種のジヒドラゾン化合物(B)が0.02~5質量部配合されているポリアセタール樹脂組成物。
- 前記一般式(1)において、R1が炭素数6~12の脂肪族炭化水素基である請求項1記載のポリアセタール樹脂組成物。
- 前記一般式(1)において、R2及びR4がエチル基である場合には、R3及びR5が水素原子であり、
R2及びR4がメチル基である場合には、R3及びR5が水素原子又はメチル基である、請求項1又は2に記載のポリアセタール樹脂組成物。 - 前記ポリアセタール樹脂(A)100質量部に対して、前記ジヒドラゾン化合物(B)が0.05~3質量部配合されている請求項1~3のいずれか一項に記載のポリアセタール樹脂組成物。
- 前記ポリアセタール樹脂(A)100質量部に対して、ヒドラジド化合物(C)が0.01~1質量部の割合でさらに配合されている、請求項1~4のいずれか一項に記載のポリアセタール樹脂組成物。
- 前記ヒドラジド化合物(C)がモノヒドラジド化合物及びジヒドラジド化合物からなる群より少なくとも1種で構成される、請求項5に記載のポリアセタール樹脂組成物。
- 前記ヒドラジド化合物(C)がジヒドラジド化合物で構成される、請求項6に記載のポリアセタール樹脂組成物。
- 請求項1~7のいずれか一項に記載のポリアセタール樹脂組成物を成形してなる樹脂成形品。
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US15/112,450 US9850367B2 (en) | 2014-01-28 | 2015-01-27 | Polyacetal resin composition and resin molded article |
EP15743411.9A EP3101067B1 (en) | 2014-01-28 | 2015-01-27 | Polyacetal resin composition, and resin molded article |
CN201580004955.7A CN105916936B (zh) | 2014-01-28 | 2015-01-27 | 聚缩醛树脂组合物和树脂成型品 |
JP2015559936A JP6541578B2 (ja) | 2014-01-28 | 2015-01-27 | ポリアセタール樹脂組成物および樹脂成形品 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2014-012893 | 2014-01-28 | ||
JP2014012893 | 2014-01-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2015115386A1 true WO2015115386A1 (ja) | 2015-08-06 |
Family
ID=53756959
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2015/052092 WO2015115386A1 (ja) | 2014-01-28 | 2015-01-27 | ポリアセタール樹脂組成物および樹脂成形品 |
Country Status (5)
Country | Link |
---|---|
US (1) | US9850367B2 (ja) |
EP (1) | EP3101067B1 (ja) |
JP (1) | JP6541578B2 (ja) |
CN (1) | CN105916936B (ja) |
WO (1) | WO2015115386A1 (ja) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2016175956A (ja) * | 2015-03-18 | 2016-10-06 | 三菱エンジニアリングプラスチックス株式会社 | 撥菌材 |
JP2017025257A (ja) * | 2015-07-27 | 2017-02-02 | 三菱エンジニアリングプラスチックス株式会社 | ポリアセタール樹脂組成物及びポリアセタール樹脂成形品 |
JP2017137386A (ja) * | 2016-02-02 | 2017-08-10 | 三菱エンジニアリングプラスチックス株式会社 | ポリアセタール樹脂組成物及びそれを用いて得られる樹脂成形品 |
JP2017206665A (ja) * | 2016-05-20 | 2017-11-24 | 三菱エンジニアリングプラスチックス株式会社 | ポリアセタール樹脂組成物、その製造方法及び樹脂成形品 |
JP2019006974A (ja) * | 2017-06-20 | 2019-01-17 | 三菱エンジニアリングプラスチックス株式会社 | ポリアセタール樹脂組成物および成形品 |
JP7462495B2 (ja) | 2020-07-08 | 2024-04-05 | グローバルポリアセタール株式会社 | 樹脂組成物および成形品 |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019056334A1 (en) * | 2017-09-25 | 2019-03-28 | Dow Global Technologies Llc | AQUEOUS POLYMER COMPOSITION |
CN113166524B (zh) * | 2018-07-26 | 2024-06-18 | 杜邦聚合物公司 | 金属-聚缩醛组合件 |
CN113652054A (zh) * | 2020-05-12 | 2021-11-16 | 旭化成株式会社 | 聚缩醛树脂组合物 |
JP7078687B2 (ja) * | 2020-10-09 | 2022-05-31 | ポリプラスチックス株式会社 | ポリアセタール樹脂組成物及び自動車部品 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005137785A (ja) * | 2003-11-10 | 2005-06-02 | Polyplastics Co | アルデヒド抑制剤組成物およびポリアセタール樹脂組成物 |
JP2005325225A (ja) * | 2004-05-14 | 2005-11-24 | Mitsubishi Engineering Plastics Corp | ポリアセタール樹脂組成物およびそれからなる成形品 |
JP2005336304A (ja) * | 2004-05-26 | 2005-12-08 | Mitsubishi Engineering Plastics Corp | ポリアセタール樹脂組成物およびそれからなる成形品 |
JP2007070574A (ja) | 2005-09-09 | 2007-03-22 | Polyplastics Co | ポリアセタール樹脂組成物及び成形品 |
JP2009084369A (ja) * | 2007-09-28 | 2009-04-23 | Adeka Corp | 合成樹脂組成物 |
JP2014501827A (ja) * | 2010-12-21 | 2014-01-23 | コンパニー ゼネラール デ エタブリッスマン ミシュラン | ヒドラジド、ヒドラゾン又はポリアミンを含む天然ゴム及びカーボンブラックをベースとする組成物 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5616102B2 (ja) * | 2010-04-08 | 2014-10-29 | 旭化成ケミカルズ株式会社 | 自動車内装・機構部品 |
-
2015
- 2015-01-27 EP EP15743411.9A patent/EP3101067B1/en active Active
- 2015-01-27 JP JP2015559936A patent/JP6541578B2/ja active Active
- 2015-01-27 US US15/112,450 patent/US9850367B2/en active Active
- 2015-01-27 CN CN201580004955.7A patent/CN105916936B/zh active Active
- 2015-01-27 WO PCT/JP2015/052092 patent/WO2015115386A1/ja active Application Filing
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005137785A (ja) * | 2003-11-10 | 2005-06-02 | Polyplastics Co | アルデヒド抑制剤組成物およびポリアセタール樹脂組成物 |
JP2005325225A (ja) * | 2004-05-14 | 2005-11-24 | Mitsubishi Engineering Plastics Corp | ポリアセタール樹脂組成物およびそれからなる成形品 |
JP2005336304A (ja) * | 2004-05-26 | 2005-12-08 | Mitsubishi Engineering Plastics Corp | ポリアセタール樹脂組成物およびそれからなる成形品 |
JP2007070574A (ja) | 2005-09-09 | 2007-03-22 | Polyplastics Co | ポリアセタール樹脂組成物及び成形品 |
JP2009084369A (ja) * | 2007-09-28 | 2009-04-23 | Adeka Corp | 合成樹脂組成物 |
JP2014501827A (ja) * | 2010-12-21 | 2014-01-23 | コンパニー ゼネラール デ エタブリッスマン ミシュラン | ヒドラジド、ヒドラゾン又はポリアミンを含む天然ゴム及びカーボンブラックをベースとする組成物 |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2016175956A (ja) * | 2015-03-18 | 2016-10-06 | 三菱エンジニアリングプラスチックス株式会社 | 撥菌材 |
JP2017025257A (ja) * | 2015-07-27 | 2017-02-02 | 三菱エンジニアリングプラスチックス株式会社 | ポリアセタール樹脂組成物及びポリアセタール樹脂成形品 |
WO2017018210A1 (ja) * | 2015-07-27 | 2017-02-02 | 三菱エンジニアリングプラスチックス株式会社 | ポリアセタール樹脂組成物及びポリアセタール樹脂成形品 |
JP2017137386A (ja) * | 2016-02-02 | 2017-08-10 | 三菱エンジニアリングプラスチックス株式会社 | ポリアセタール樹脂組成物及びそれを用いて得られる樹脂成形品 |
JP2017206665A (ja) * | 2016-05-20 | 2017-11-24 | 三菱エンジニアリングプラスチックス株式会社 | ポリアセタール樹脂組成物、その製造方法及び樹脂成形品 |
JP2019006974A (ja) * | 2017-06-20 | 2019-01-17 | 三菱エンジニアリングプラスチックス株式会社 | ポリアセタール樹脂組成物および成形品 |
JP7462495B2 (ja) | 2020-07-08 | 2024-04-05 | グローバルポリアセタール株式会社 | 樹脂組成物および成形品 |
Also Published As
Publication number | Publication date |
---|---|
JP6541578B2 (ja) | 2019-07-10 |
JPWO2015115386A1 (ja) | 2017-03-23 |
EP3101067A4 (en) | 2017-09-06 |
US20160333170A1 (en) | 2016-11-17 |
US9850367B2 (en) | 2017-12-26 |
EP3101067B1 (en) | 2018-05-16 |
EP3101067A1 (en) | 2016-12-07 |
CN105916936A (zh) | 2016-08-31 |
CN105916936B (zh) | 2018-11-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6541578B2 (ja) | ポリアセタール樹脂組成物および樹脂成形品 | |
US10131782B2 (en) | Polyoxymethylene compositions, method of manufacture, and articles made therefrom | |
JP6062614B2 (ja) | ポリアセタール樹脂組成物 | |
EP3330317B1 (en) | Polyacetal resin composition and polyacetal resin molded article | |
JP5752986B2 (ja) | ポリアセタール樹脂組成物及びそれからなる成形品 | |
JP5661437B2 (ja) | ポリアセタール樹脂組成物 | |
JP2012233131A (ja) | ポリアセタール樹脂組成物及びそれからなる成形品 | |
JP2012092185A (ja) | ポリアセタール樹脂組成物及びそれからなる成形品 | |
JP5936335B2 (ja) | ポリアセタール樹脂組成物 | |
CN108026352B (zh) | 聚缩醛树脂组合物及其成型体 | |
JP2007145979A (ja) | ポリアセタール樹脂組成物及び成形品 | |
JP5890754B2 (ja) | ポリアセタール樹脂組成物 | |
JP4845174B2 (ja) | ポリアセタール樹脂組成物およびそれを含む樹脂成形品 | |
JP2013028737A (ja) | ポリオキシメチレン樹脂組成物及びそれからなる成形品 | |
JP2005162909A (ja) | ポリアセタール樹脂組成物およびそれからなる成形品 | |
JP2013100393A (ja) | ポリアセタール樹脂組成物 | |
JP2005263921A (ja) | ポリアセタール樹脂組成物およびそれからなる成形品 | |
JP2012107150A (ja) | ポリアセタール樹脂組成物及びそれからなる成形品 | |
JP2014005385A (ja) | ポリアセタール樹脂組成物 | |
JP2006045331A (ja) | ポリアセタール樹脂組成物およびそれからなる成形品 | |
JP2005171158A (ja) | ポリアセタール樹脂組成物及びそれからなる成形品 | |
JP2017137386A (ja) | ポリアセタール樹脂組成物及びそれを用いて得られる樹脂成形品 | |
JP2013103958A (ja) | ポリアセタール樹脂組成物 | |
JP2006045333A (ja) | ポリアセタール樹脂組成物およびそれからなる成形品 | |
JP2005179593A (ja) | ポリアセタール樹脂組成物およびそれからなる成形品 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 15743411 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 2015559936 Country of ref document: JP Kind code of ref document: A |
|
WWE | Wipo information: entry into national phase |
Ref document number: 15112450 Country of ref document: US |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
REEP | Request for entry into the european phase |
Ref document number: 2015743411 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2015743411 Country of ref document: EP |