WO2014208633A1 - Flame retardant composition and molded article including the same - Google Patents
Flame retardant composition and molded article including the same Download PDFInfo
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- WO2014208633A1 WO2014208633A1 PCT/JP2014/066918 JP2014066918W WO2014208633A1 WO 2014208633 A1 WO2014208633 A1 WO 2014208633A1 JP 2014066918 W JP2014066918 W JP 2014066918W WO 2014208633 A1 WO2014208633 A1 WO 2014208633A1
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- WIPO (PCT)
- Prior art keywords
- flame retardant
- weight
- retardant composition
- percent
- content
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 65
- 239000003063 flame retardant Substances 0.000 title claims abstract description 63
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 title claims abstract description 62
- 229920001971 elastomer Polymers 0.000 claims abstract description 31
- 229920002678 cellulose Polymers 0.000 claims abstract description 30
- 239000001913 cellulose Substances 0.000 claims abstract description 27
- 239000012757 flame retardant agent Substances 0.000 claims abstract description 23
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 20
- 229920005989 resin Polymers 0.000 claims description 22
- 239000011347 resin Substances 0.000 claims description 22
- 150000001875 compounds Chemical class 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 15
- 229920007019 PC/ABS Polymers 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 238000002156 mixing Methods 0.000 claims description 7
- 238000004898 kneading Methods 0.000 claims description 6
- 238000000465 moulding Methods 0.000 claims description 5
- 238000001125 extrusion Methods 0.000 claims description 3
- 238000001746 injection moulding Methods 0.000 claims description 3
- 235000010980 cellulose Nutrition 0.000 description 22
- 238000012360 testing method Methods 0.000 description 15
- -1 boric acid compound Chemical class 0.000 description 11
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 10
- 239000004810 polytetrafluoroethylene Substances 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 8
- 239000008188 pellet Substances 0.000 description 7
- 229910019142 PO4 Inorganic materials 0.000 description 6
- 229920000297 Rayon Polymers 0.000 description 6
- 239000010452 phosphate Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 239000000835 fiber Substances 0.000 description 5
- 239000003963 antioxidant agent Substances 0.000 description 3
- 230000003078 antioxidant effect Effects 0.000 description 3
- 239000011258 core-shell material Substances 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 229920000515 polycarbonate Polymers 0.000 description 3
- 239000004417 polycarbonate Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 238000004513 sizing Methods 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- 239000006087 Silane Coupling Agent Substances 0.000 description 2
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 2
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 2
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 2
- 239000008108 microcrystalline cellulose Substances 0.000 description 2
- 229940016286 microcrystalline cellulose Drugs 0.000 description 2
- 239000013500 performance material Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920000747 poly(lactic acid) Polymers 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 229910000077 silane Inorganic materials 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- OWICEWMBIBPFAH-UHFFFAOYSA-N (3-diphenoxyphosphoryloxyphenyl) diphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=C(OP(=O)(OC=2C=CC=CC=2)OC=2C=CC=CC=2)C=CC=1)(=O)OC1=CC=CC=C1 OWICEWMBIBPFAH-UHFFFAOYSA-N 0.000 description 1
- ZMKVBUOZONDYBW-UHFFFAOYSA-N 1,6-dioxecane-2,5-dione Chemical compound O=C1CCC(=O)OCCCCO1 ZMKVBUOZONDYBW-UHFFFAOYSA-N 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000219146 Gossypium Species 0.000 description 1
- 240000000797 Hibiscus cannabinus Species 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 241001618237 Peltophorum africanum Species 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- BQPNUOYXSVUVMY-UHFFFAOYSA-N [4-[2-(4-diphenoxyphosphoryloxyphenyl)propan-2-yl]phenyl] diphenyl phosphate Chemical compound C=1C=C(OP(=O)(OC=2C=CC=CC=2)OC=2C=CC=CC=2)C=CC=1C(C)(C)C(C=C1)=CC=C1OP(=O)(OC=1C=CC=CC=1)OC1=CC=CC=C1 BQPNUOYXSVUVMY-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- APOXBWCRUPJDAC-UHFFFAOYSA-N bis(2,6-dimethylphenyl) hydrogen phosphate Chemical compound CC1=CC=CC(C)=C1OP(O)(=O)OC1=C(C)C=CC=C1C APOXBWCRUPJDAC-UHFFFAOYSA-N 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000012796 inorganic flame retardant Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
- C08L1/02—Cellulose; Modified cellulose
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/08—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds
- C08L51/085—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds on to polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L55/00—Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
- C08L55/02—ABS [Acrylonitrile-Butadiene-Styrene] polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K21/00—Fireproofing materials
- C09K21/06—Organic materials
- C09K21/12—Organic materials containing phosphorus
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G21/00—Arrangements not provided for by groups G03G13/00 - G03G19/00, e.g. cleaning, elimination of residual charge
- G03G21/16—Mechanical means for facilitating the maintenance of the apparatus, e.g. modular arrangements
- G03G21/1604—Arrangement or disposition of the entire apparatus
- G03G21/1619—Frame structures
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0066—Flame-proofing or flame-retarding additives
-
- 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
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
-
- 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
- C08K9/00—Use of pretreated ingredients
- C08K9/04—Ingredients treated with organic substances
- C08K9/06—Ingredients treated with organic substances with silicon-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/02—Flame or fire retardant/resistant
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/08—Stabilised against heat, light or radiation or oxydation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/20—Applications use in electrical or conductive gadgets
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- 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
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
Definitions
- the present invention relates to a flame retardant composition .
- PTL 1 has disclosed a method in which after the flame retardancy is imparted to natural fibers using boric acid or a boric acid compound, the natural fibers are compounded with a resin to form a flame retardant resin composition while a high heat resistance and a high rigidity are maintained.
- the flame retardancy of the disclosed resin composition was rated as UL-94 V-l, and a high flame retardancy (UL-94 5VB) required, for example, for housings of office machines could not be obtained .
- the present invention provides a flame retardant composition having a high flame retardancy and high mechanical properties, the flame retardant composition including a thermoplastic resin, a cellulose, a rubber having a siloxane bond, and a. flame retardant agent.
- the present invention relates to a flame retardant composition including a thermoplastic resin, a cellulose, a rubber having a siloxane bond, and a flame retardant agent.
- a flame retardant composition including a thermoplastic resin, a cellulose, a rubber having a siloxane bond, and a flame retardant agent.
- the content of the flame retardant composition when the weight of the flame retardant composition is set to 100 percent by weight, the content of the thermoplastic resin is 50 to 90 percent by weight, the content of the cellulose is 1 to 30 percent by weight, the content of the rubber having a siloxane bond is 3 to 20 percent by weight, and the content of the flame retardant agent is 5 to 20 percent by weight.
- FIG. 1A is an external view showing one example of an image forming apparatus according to an embodiment.
- Fig. IB is a schematic view showing the inside of one example of the image forming apparatus according to the embodiment .
- a flame retardant composition of the present invention includes a thermoplastic resin, a cellulose, a rubber having a siloxane bond, and a flame retardant agent.
- the thermoplastic resin is called an A
- the cellulose is called a B component
- the rubber having a siloxane bond is called a C component
- the flame retardant agent is called a D component in some cases.
- the flame retardant composition of the present invention has a high flame retardancy and is rated as UL-94 5VB.
- the flame retardant composition of the present invention includes a thermoplastic resin.
- the content of the thermoplastic resin is preferably 50 to 90 percent by weight.
- thermoplastic resin of the present invention for example, a polyethylene (PE), a polypropylene (PP), a polystyrene (PS), a polycarbonate (PC), a poly (ethylene terephthalate) (PET), a poly (butylene terephthalate ) ( PBT) , a poly (lactic acid) (PLA) , a poly (butylene succinate) (PBS), an acrylonitrile-butadiene-styrene copolymer compound (ABS) , a styrene-acrylonitrile copolymer compound (SAN) , and a polymer alloy, such as PC/ABS or PC/SAN, may be mentioned.
- Those resins may be used alone, or at least two types
- PC/ABS and PC/SAN are preferable.
- the flame retardant composition of the present invention includes a cellulose.
- the content of the cellulose is preferably 1 to 30 percent by weight and more preferably 3 to 15 percent by weight.
- the flame retardant composition can obtain sufficient impact strength and flame retardancy.
- a compound primarily formed of a cellulose may be used, and any compound extracted from a plant or formed by a chemical synthesis may be used.
- the cellulose is not limited, for example, by the manufacturing method, the shape, and the degree of crystallization thereof. As particular examples of the cellulose, for example, there may be
- bamboo powder wood powder, kenaf, flax, cotton, jute, used paper, wood pulp, microcrystalline cellulose, and microfibrillated cellulose.
- celluloses mentioned above may be used alone, or at least two types thereof may be used in combination.
- a cellulose having a fiber shape and a fiber diameter of 100 ⁇ or less is preferably used.
- a molded article may be provided without degrading the appearance thereof.
- a known surface treatment may be performed on the celluloses mentioned above.
- a surface treatment method for example, a sizing treatment, a silane coupling treatment, or an esterification treatment may be mentioned. Among those mentioned above, a sizing treatment and a silane coupling treatment are preferable.
- the flame retardant composition of the present invention includes a rubber having a siloxane bond.
- the content of the rubber having a siloxane bond is preferably 3 to 20 percent by weight and more preferably 5 to 15 percent by weight.
- the rubber having a siloxane bond of the present invention is a rubber having a siloxane bond in a polymer structure.
- thermoplastic resin is preferable, and as a particular example, a silicone rubber may be mentioned, or in more particular, a silicone-acrylic-based core-shell rubber may be mentioned.
- the core-shell rubber is a rubber having a core portion and a shell portion.
- the silicone-acrylic-based core-shell rubber has, for example, a silicone-acrylic composite rubber as the core portion and a graft layer of a vinyl-based polymer as the shell portion.
- the flame retardant composition of the present invention includes a flame retardant agent.
- the content of the flame retardant agent is
- the content of the flame retardant agent is set to 5 to 20 percent by weight, a high impact strength and a sufficient flame retardancy can be obtained.
- an organic flame retardant agent such as triphenyl phosphate, tricresyl phosphate, or trixylyl phosphate
- a condensed phosphate ester such as resorcinol bis (diphenyl phosphate), bisphenol A bis (diphenyl phosphate), or resorcinol bis (di- 2,6-xylyl phosphate).
- a commercially available condensed phosphate ester for example, CR-733S, CR-741, and PX-200, each manufactured by Daihachi Chemical Industry Co., Ltd., may be mentioned.
- the flame retardant composition of the present invention may further include an anti-dripping agent, a pigment, a thermal stabilizer, an antioxidant, an inorganic filler, a weather resistant agent, a lubricant, a mold- releasing agent, an antistatic agent, and the like as long as the properties of the flame retardant composition are not impaired.
- an anti-dripping agent a pigment, a thermal stabilizer, an antioxidant, an inorganic filler, a weather resistant agent, a lubricant, a mold- releasing agent, an antistatic agent, and the like.
- composition is set to 100 percent by weight, 20 percent by weight or less of the above additives may be contained.
- the flame retardant composition of the present invention may also include a fluorinated compound.
- the fluorinated compound functions as an anti-dripping agent.
- the type of fluorinated compound is not
- P FE polytetrafluoroethylene
- the content of the fluorinated compound (E component) included in the flame retardant composition of this embodiment is preferably 0.1 to 1.0 percent by weight.
- the content is less than 0.1 percent by weight, a resin is melted and dripped from a flame-retardant test piece when a flame is brought into contact therewith, and as a result, the flame retardancy is difficult to be rated as UL-94 5BV.
- PTFE polytetrafluoroethylene
- Metablen A-3800 (trade name, manufactured by Mitsubishi Rayon Co. Ltd.), which is an acrylic resin- modified PTFE, may be mentioned.
- the . ratio between charge amounts may be regarded as the composition ratio of the composition.
- the composition ratio of the composition may also be measured.
- a molded article including the flame retardant composition of the present invention may have a desired shape by molding. Although a molding method is not
- extrusion molding or injection molding particularly limited, for example, a known technique, such as extrusion molding or injection molding, may be used.
- extrusion molding or injection molding is preferably used.
- composition of this embodiment may be a recovered resin.
- the flame retardant composition may be called a recycle resin.
- the recycle resin is manufactured, a cellulose, a rubber having a siloxane bond, and a flame retardant agent may be added to a prepared resin.
- melt-kneading performed by a kneading machine is preferable.
- the recovered resin may be obtained from a
- recovered molded article for example, housings of image forming apparatuses, camera components, housings and internal components of personal computers, housings and internal components of television sets, and water bottles may be mentioned.
- the molded articles of this embodiment may be used for components, each of which is required to have flame retardancy, of image forming .
- apparatuses such as a copying machine, a laser beam printer, and an ink jet printer.
- a housing accommodating a
- photosensitive member a component provided around a fixing device, and a component provided around a power source may be mentioned.
- the molded article may also be used as an exterior member as long as the design characteristics are not adversely influenced.
- an apparatus shown in Figs. 1A and IB may be mentioned.
- Fig. 1A is an external view showing one example of the image forming apparatus.
- the exterior members are shown in Fig. 1A.
- Fig. IB is a schematic view showing the inside of one example of the image forming apparatus. The internal
- PC/ABS (808 g) , a silicone-acrylic-based rubber (50 g, Metablen SX-005, manufactured by Mitsubishi Rayon Co.
- melt-kneading was performed at a cylinder temperature of 240°C to 250°C by a biaxial extruder
- Performance Materials, Inc. to have a content of 1 percent by weight were weighed and mixed together.
- melt-kneading was performed at a cylinder temperature of 200°C to 210°C by a biaxial extruder
- multipurpose test pieces (each having a size of 80 mmxlO mmxt (thickness) 4 mm) were molded at a cylinder temperature of 210°C to 230°C and at a mold temperature of 60°C, and flame-retardant test pieces (each having a size of 125 mmxl2.5 mmxt 2 mm) were molded at a cylinder temperature of 210°C to 230°C and at a mold temperature of 40°C.
- Silane coupling agent "Silquest A-1110" manufactured by manufactured by Momentive Performance Materials, Inc.
- Test method In accordance with the 5V test of UL-94 (125 mm vertical burning test)
- Sample shape Multipurpose test piece (80 mmxlO mmxt 4 mm) Notch machining: The type A notch is formed using a notching tool A-3 (manufactured by Toyo Seiki Sei.saku-sho, Ltd.).
- Measurement device Digital impact test machine DG-UB
- Placement method flat placement
- Measurement device HDT/VSPT test device TM-4126 (manufactured by Ueshima Seisakusho Co., Ltd.)
- cellulose, the rubber having a siloxane bond, and the flame retardant agent are blended together, a flame retardancy of 5VB, a Charpy impact strength of 5 kJ/m 2 or more, and a deflection temperature under load of 70°C or more were obtained as the evaluation results.
- a flame retardant composition having a low environment load, a high flame retardancy, and high
- mechanical properties may be used as a molding material for office machine housings, electric/electronic components, automobile components, building components, and the like.
- thermoplastic resin a thermoplastic resin
- cellulose a cellulose
- rubber having a siloxane bond a thermoplastic resin
- flame retardant agent a flame retardant agent
- a retardant composition having a high flame retardancy and high mechanical properties can be provided.
- a molded article having a high flame retardancy can be provided.
Abstract
The present invention provides a flame retardant composition including a thermoplastic resin, a cellulose, a rubber having a siloxane bond, and a flame retardant agent.
Description
DESCRIPTION
FLAME RETARDANT COMPOSITION AND MOLDED ARTICLE
INCLUDING THE SAME
Technical Field
[0001] The present invention relates to a flame retardant composition .
Background Art
[0002] In recent years, in consideration of emission reduction of carbon dioxide and usage reduction of fossil resources which might be depleted in near future, research and development of low environmental load resins has been actively carried out using bio-renewable raw materials, and in particular, attention has been paid to the use of
celluloses which occur abundantly · in nature.
[0003] However, when a cellulose is compounded with a resin, although the heat resistance and the rigidity of the resin are improved, the impact strength and the flame retardancy thereof are remarkably degraded. Hence, a method for improving the impact strength and the flame retardancy has been pursued.
[0004] In order to solve the problem described above, PTL 1 has disclosed a method in which after the flame retardancy is imparted to natural fibers using boric acid or a boric
acid compound, the natural fibers are compounded with a resin to form a flame retardant resin composition while a high heat resistance and a high rigidity are maintained.
[0005] According to PTL 1, an attempt was performed to improve the flame retardancy and mechanical properties, such as the impact strength and the heat resistance, of a
cellulose composite thermoplastic resin. However, the flame retardancy of the disclosed resin composition was rated as UL-94 V-l, and a high flame retardancy (UL-94 5VB) required, for example, for housings of office machines could not be obtained .
Citation List
Patent Literature
[0006] PTL 1 Japanese Patent Laid-Open No. 2007-231034 Summary of Invention
[0007] Accordingly, the present invention provides a flame retardant composition having a high flame retardancy and high mechanical properties, the flame retardant composition including a thermoplastic resin, a cellulose, a rubber having a siloxane bond, and a. flame retardant agent.
[0008] Hence, the present invention relates to a flame retardant composition including a thermoplastic resin, a cellulose, a rubber having a siloxane bond, and a flame retardant agent. In the flame retardant composition
described above, when the weight of the flame retardant
composition is set to 100 percent by weight, the content of the thermoplastic resin is 50 to 90 percent by weight, the content of the cellulose is 1 to 30 percent by weight, the content of the rubber having a siloxane bond is 3 to 20 percent by weight, and the content of the flame retardant agent is 5 to 20 percent by weight.
[0009] Further features of the present invention will become apparent from the following description of exemplary embodiments with reference to the attached drawings.
Brief Description of Drawings
[0010] Fig. 1A is an external view showing one example of an image forming apparatus according to an embodiment.
[0011] Fig. IB is a schematic view showing the inside of one example of the image forming apparatus according to the embodiment .
Description of Embodiments
[0012] A flame retardant composition of the present invention includes a thermoplastic resin, a cellulose, a rubber having a siloxane bond, and a flame retardant agent. Hereinafter, the thermoplastic resin is called an A
component, the cellulose is called a B component, the rubber having a siloxane bond is called a C component, and the flame retardant agent is called a D component in some cases.
[0013] The flame retardant composition of the present invention has a high flame retardancy and is rated as UL-94
5VB.
[0014] The flame retardant composition of the present invention includes a thermoplastic resin. When the weight of the flame retardant composition is set to 100 percent by weight, the content of the thermoplastic resin is preferably 50 to 90 percent by weight.
[0015] As the thermoplastic resin of the present invention, for example, a polyethylene (PE), a polypropylene (PP), a polystyrene (PS), a polycarbonate (PC), a poly (ethylene terephthalate) (PET), a poly (butylene terephthalate ) ( PBT) , a poly (lactic acid) (PLA) , a poly (butylene succinate) (PBS), an acrylonitrile-butadiene-styrene copolymer compound (ABS) , a styrene-acrylonitrile copolymer compound (SAN) , and a polymer alloy, such as PC/ABS or PC/SAN, may be mentioned. Those resins may be used alone, or at least two types
thereof may be used in combination. In particular, PC/ABS and PC/SAN are preferable.
[0016] The flame retardant composition of the present invention includes a cellulose. When the weight of the flame retardant composition is set to 100 percent by weight, the content of the cellulose is preferably 1 to 30 percent by weight and more preferably 3 to 15 percent by weight.
[0017] When the content of the cellulose is 30 percent by weight or less., the flame retardant composition can obtain sufficient impact strength and flame retardancy.
[0018] As the cellulose of the present invention, a compound primarily formed of a cellulose may be used, and any compound extracted from a plant or formed by a chemical synthesis may be used. In addition, the cellulose is not limited, for example, by the manufacturing method, the shape, and the degree of crystallization thereof. As particular examples of the cellulose, for example, there may be
mentioned bamboo powder, wood powder, kenaf, flax, cotton, jute, used paper, wood pulp, microcrystalline cellulose, and microfibrillated cellulose.
[0019] Those celluloses mentioned above may be used alone, or at least two types thereof may be used in combination.
In particular, a cellulose having a fiber shape and a fiber diameter of 100 μπι or less is preferably used. When the fiber diameter is 100 μπι or less, a molded article may be provided without degrading the appearance thereof.
[0020] In addition, a known surface treatment may be performed on the celluloses mentioned above. As a surface treatment method, for example, a sizing treatment, a silane coupling treatment, or an esterification treatment may be mentioned. Among those mentioned above, a sizing treatment and a silane coupling treatment are preferable.
[0021] The flame retardant composition of the present invention includes a rubber having a siloxane bond. When the weight of the flame retardant composition is set to 100
percent by weight, the content of the rubber having a siloxane bond is preferably 3 to 20 percent by weight and more preferably 5 to 15 percent by weight.
[ 0022 ] When the content of the rubber having a siloxane bond is set to 3 to 20 percent by weight, a high impact strength and a high flame retardancy can be obtained.
[ 0023 ] The rubber having a siloxane bond of the present invention is a rubber having a siloxane bond in a polymer structure. A rubber having a high affinity for a
thermoplastic resin is preferable, and as a particular example, a silicone rubber may be mentioned, or in more particular, a silicone-acrylic-based core-shell rubber may be mentioned.
[ 0024 ] The core-shell rubber is a rubber having a core portion and a shell portion. The silicone-acrylic-based core-shell rubber has, for example, a silicone-acrylic composite rubber as the core portion and a graft layer of a vinyl-based polymer as the shell portion.
[ 0025 ] The flame retardant composition of the present invention includes a flame retardant agent. When the weight of the flame retardant composition is set to 100 percent by weight, the content of the flame retardant agent is
preferably 5 to 20 percent by weight.
[0026] When the content of the flame retardant agent is set to 5 to 20 percent by weight, a high impact strength and
a sufficient flame retardancy can be obtained.
[0027] As the flame retardant agent of the present
invention, an organic flame retardant agent, an inorganic flame retardant agent, or a mixture therebetween may be used. A phosphorus-based flame retardant agent is preferable. As particular examples thereof, for example, there may be mentioned a phosphate ester, such as triphenyl phosphate, tricresyl phosphate, or trixylyl phosphate; or a condensed phosphate ester, such as resorcinol bis (diphenyl phosphate), bisphenol A bis (diphenyl phosphate), or resorcinol bis (di- 2,6-xylyl phosphate). As a commercially available condensed phosphate ester, for example, CR-733S, CR-741, and PX-200, each manufactured by Daihachi Chemical Industry Co., Ltd., may be mentioned.
[0028] The flame retardant composition of the present invention may further include an anti-dripping agent, a pigment, a thermal stabilizer, an antioxidant, an inorganic filler, a weather resistant agent, a lubricant, a mold- releasing agent, an antistatic agent, and the like as long as the properties of the flame retardant composition are not impaired. When the weight of the flame retardant
composition is set to 100 percent by weight, 20 percent by weight or less of the above additives may be contained.
[0029] The flame retardant composition of the present invention may also include a fluorinated compound. The
fluorinated compound functions as an anti-dripping agent. Although the type of fluorinated compound is not
particularly limited, because of good handling properties and dispersibility, a polytetrafluoroethylene (hereinafter referred to as " P FE" ) , a PTFE modified with another resin, or a PTFE-containing mixture is preferably used.
[0030] When the weight of the flame retardant compound is set to 100 percent by weight, the content of the fluorinated compound (E component) included in the flame retardant composition of this embodiment is preferably 0.1 to 1.0 percent by weight. When the content is less than 0.1 percent by weight, a resin is melted and dripped from a flame-retardant test piece when a flame is brought into contact therewith, and as a result, the flame retardancy is difficult to be rated as UL-94 5BV.
[0031] In addition, in consideration of the influence on the environment, when the total flame retardant composition of this embodiment is set to 100 percent by weight, the content of the PTFE included in the composition is
preferably 0.5 percent by weight or less.
[0032] For example, in the case of a fluorinated compound containing 50 percent by weight of a PTFE, when the weight of the flame retardant composition is set to 100 percent by weight, the content of the fluorinated compound is
preferably set to 1.0 percent by weight or less.
[ 0033 ] Although the type of fluorinated compound (E component) used in the present invention is not particularly limited, since being excellent in handling properties and dispersibility, a polytetrafluoroethylene (hereinafter referred to as " PTFE" ) , a PTFE modified with another resin, or a PTFE-containing mixture is preferably used. In
particular, Metablen A-3800 (trade name, manufactured by Mitsubishi Rayon Co. Ltd.), which is an acrylic resin- modified PTFE, may be mentioned.
[ 0034 ] As for the weight ratio of the flame retardant composition of the present invention, the. ratio between charge amounts may be regarded as the composition ratio of the composition. Alternatively, by the measurement of a molded article by instrumental analysis using NMR, pyrolytic GC/MS, or the like, the composition ratio of the composition may also be measured.
[ 0035] A molded article including the flame retardant composition of the present invention may have a desired shape by molding. Although a molding method is not
particularly limited, for example, a known technique, such as extrusion molding or injection molding, may be used. In particular, extrusion molding or injection molding is preferably used.
[0036 ] The resin included in the flame retardant
composition of this embodiment may be a recovered resin.
When a recovered resin is used, the flame retardant composition may be called a recycle resin. When the recycle resin is manufactured, a cellulose, a rubber having a siloxane bond, and a flame retardant agent may be added to a prepared resin.
[0037] Although a mixing method used for the addition is not particularly limited, melt-kneading performed by a kneading machine is preferable.
[0038] The recovered resin may be obtained from a
recovered molded article. As the recovered molded articles, for example, housings of image forming apparatuses, camera components, housings and internal components of personal computers, housings and internal components of television sets, and water bottles may be mentioned.
[0039] The molded articles of this embodiment may be used for components, each of which is required to have flame retardancy, of image forming .apparatuses, such as a copying machine, a laser beam printer, and an ink jet printer. In particular,' for example, a housing accommodating a
photosensitive member, a component provided around a fixing device, and a component provided around a power source may be mentioned.
[0040] In addition, the molded article may also be used as an exterior member as long as the design characteristics are not adversely influenced.
[0041] As the image forming apparatus, for example, an apparatus shown in Figs. 1A and IB may be mentioned. Fig. 1A is an external view showing one example of the image forming apparatus. The exterior members are shown in Fig. 1A. Fig. IB is a schematic view showing the inside of one example of the image forming apparatus. The internal
components are shown in Fig. IB.
Examples
Example 1
[0042] PC/ABS (Cycoloy C1200HF manufactured by SABIC
Innovative Plastics) was dried at 80°C for 6 hours.
[0043] PC/ABS (808 g) , a silicone-acrylic-based rubber (50 g, Metablen SX-005, manufactured by Mitsubishi Rayon Co.
Ltd.), a condensed phosphate ester-based flame retardant agent (100 g, PX-200, manufactured by Daihachi Chemical
Industry Co., Ltd.), an anti-dripping agent (10 g, Metablen A-3800, manufactured by Mitsubishi Rayon Co. Ltd.), and an antioxidant (2 g, Irganox B220, manufactured by BASF) were weighed and mixed together.
[0044] Next, melt-kneading was performed at a cylinder temperature of 240°C to 250°C by a biaxial extruder
(Laboplasto Mill, manufactured by Toyo Seiki Seisaku-sho, Ltd.). A resin extruded from a front end of the extruder is cut into pellets, so that pellets of the resin were obtained. The pellets thus obtained were dried at 80°C for 6 hours.
[0045] Subsequently, 970 g of the pellets described above and 30 g of a cotton powder processed with a silane coupling agent (Silquest A-1110, manufactured by Momentive
Performance Materials, Inc.,) to have a content of 1 percent by weight were weighed and mixed together.
[0046] Next, melt-kneading was performed at a cylinder temperature of 200°C to 210°C by a biaxial extruder
(Laboplasto Mill, manufactured by Toyo Seiki Seisaku-sho, Ltd. ) . A resin extruded from a front end of the extruder is cut into pellets, so that pellets of the resin were obtained.
[0047] After the pellets thus obtained were dried at 80°C for 6 hours, by using an injection machine (SE18DU,
manufactured by Sumitomo Heavy Industries, Ltd:),
multipurpose test pieces (each having a size of 80 mmxlO mmxt (thickness) 4 mm) were molded at a cylinder temperature of 210°C to 230°C and at a mold temperature of 60°C, and flame-retardant test pieces (each having a size of 125 mmxl2.5 mmxt 2 mm) were molded at a cylinder temperature of 210°C to 230°C and at a mold temperature of 40°C.
Examples 2 to 9
[0048] Raw materials were mixed together at a mass ratio as shown in Table 1. Except for that described above,
multipurpose test pieces and flame-retardant test pieces were molded using a resin in a manner similar to that in
Example 1.
Comparative Examples 1 to 3
[0049] Raw materials were mixed together at a mass ratio as shown in Table 1. Except for that described above, multipurpose test pieces and flame-retardant test pieces were molded using a resin in a manner similar to that in Example 1.
[0050] As the materials shown in Table 1, the following materials were used.
• PC/ABS "Cycoloy C1200HF" manufactured by SABIC Innovative Plastics .
• Microcrystalline cellulose "Ceolus ST-100" manufactured by Asahi Kasei Chemicals Corporation.
• Silane coupling agent "Silquest A-1110" manufactured by manufactured by Momentive Performance Materials, Inc.
• Sizing agent "SIZEPINE K-931" manufactured by Arakawa Chemical industries, Ltd.
• Silicone-acrylic-based rubber "Metablen SX-005"
manufactured by Mitsubishi Rayon Co. Ltd.
• Condensed phosphate ester-based flame retardant agent "PX- 200" manufactured by Daihachi Chemical Industry Co., Ltd.
• MBS-based rubber "Metablen C-223A" manufactured by
Mitsubishi Rayon Co. Ltd.
• Talc "High Micron HE5" manufactured by Takehara Chemical Industry . Co . , Ltd.
• Anti-dripping agent "Metablen A-3800" manufactured by
Mitsubishi Rayon Co. Ltd.
• Antioxidant "Irganox B220" manufactured by BASF.
In addition, as the evaluation, the following tests were performed.
[0051] (1) Flame retardancy
Test method: In accordance with the 5V test of UL-94 (125 mm vertical burning test)
Sample shape: Flame-retardant test piece (125 mmxl2.5 mmxt 2 mm)
(2) Charpy impact strength
Test method: In accordance with JIS K 7111
Sample shape: Multipurpose test piece (80 mmxlO mmxt 4 mm) Notch machining: The type A notch is formed using a notching tool A-3 (manufactured by Toyo Seiki Sei.saku-sho, Ltd.). Measurement device: Digital impact test machine DG-UB
(manufactured by Toyo Seiki Seisaku-sho, Ltd.)
(3) Deflection temperature under load
Test method: In .accordance with JIS K 7191-2
Sample shape: Multipurpose test piece (80 mmxlO mmxt 4 mm)
Placement method: flat placement
Flexural stress: 1.80 MPa
Span length: 64 mm
Temperature rise rate: 120°C/h
Heat medium: silicone oil
Measurement device: HDT/VSPT test device TM-4126
(manufactured by Ueshima Seisakusho Co., Ltd.)
The mixing ratio and the evaluation results of the flame retardancy, the Charpy impact strength, the deflection temperature under load of each of Examples 1 to 9 and
Comparative Examples 1 to 3 are shown in Table 1.
[0052] As apparent from Table 1, when PC/ABS, the
cellulose, the rubber having a siloxane bond, and the flame retardant agent are blended together, a flame retardancy of 5VB, a Charpy impact strength of 5 kJ/m2 or more, and a deflection temperature under load of 70°C or more were obtained as the evaluation results.
[0053] On the other hand, when the rubber having a siloxane bond is not used, the 5VB test was not passed, and the Charpy impact strength was also low.
[0054]
Table 1-1
Table 1-2
[ 0056] A flame retardant composition having a low environment load, a high flame retardancy, and high
mechanical properties may be used as a molding material for office machine housings, electric/electronic components, automobile components, building components, and the like.
[0057 ] According to the present invention, since including a thermoplastic resin, a cellulose, a rubber having a siloxane bond, and a flame retardant agent, a flame
retardant composition having a high flame retardancy and high mechanical properties can be provided. In addition, a molded article having a high flame retardancy can be
provided using the flame retardant composition described above .
[0058 ] While the present invention has been described with reference to exemplary embodiments, it is to be understood that the invention is not limited to the disclosed exemplary embodiments. The scope of the following claims is to be accorded the broadest interpretation so as to encompass all such modifications and equivalent structures and functions.
[0059] This application claims the benefit of Japanese Patent Application No. 2013-136156, filed June 28, 2013, which is hereby incorporated by reference herein in its entirety .
Claims
[1] A flame retardant composition comprising:
a thermoplastic resin;
a cellulose;
a rubber having a siloxane bond; and
a flame retardant agent,
wherein when the weight of the flame retardant
composition is set to 100 percent by weight,
the content of the thermoplastic resin is 50 t.o 90 percent by weight,
the content of the cellulose is 1 to 30 percent by weight,
the content of the rubber having a siloxane bond is 3 to 20 percent by weight, and
the content of the flame retardant agent is 5 to 20 percent by weight.
[2] The flame retardant composition according to Claim 1, wherein when the weight of the flame retardant
composition is set to 100 percent by weight, the content of the cellulose is 3 to 15 percent by weight.
[3] The flame retardant composition according to Claim 1 or 2,
wherein when the weight of the flame retardant
composition is set to 100 percent by "weight, the content of
the rubber having a siloxane bond is 5 to 15 percent by weight .
[4] The flame retardant composition according to any one of Claims 1 to 3,
wherein the thermoplastic resin includes at least one of PC/ABS and PC/SA .
[5] The flame retardant composition according to any one of
Claims 1 to 4,
further comprising a fluorinated compound,
wherein when the weight of the flame retardant
composition is set to 100 percent by weight, the content of the fluorinated compound is 0.1 to 1.0 percent by weight.
[6] The flame retardant composition according to any one of
Claims 1 to 5,
wherein the flame retardant composition is rated as UL- 94 5VB.
[7] The flame retardant composition according to any one of Claims 1 to 6,
wherein the thermoplastic resin is a recovered resin. ■
[8] A molded article obtained by molding the flame
retardant composition according to any one of Claims 1 to 7.
[9] An image forming apparatus comprising:
a photosensitive member; and
a housing accommodating the photosensitive member, wherein the housing includes the molded article
according to Claim 8.
[10] A method for manufacturing a flame retardant
composition, the method comprising:
mixing, a thermoplastic resin, a cellulose, a rubber having a siloxane bond, and a flame retardant agent,
wherein when the weight of the flame retardant
composition is set to 100 percent by weight, the mixing is performed so that the content of the thermoplastic resin is 50 to 90 percent by weight, the content of the cellulose is 1 to 30 percent by weight, the content of the rubber having a siloxane bond is 3 to 20 percent by weight, and the content of the flame retardant agent is 5 to 20 percent by weight .
[11] The method for manufacturing a flame retardant
composition according to Claim 10,
further comprising mixing a fluorinated compound with the thermoplastic resin, the cellulose, the rubber having a siloxane bond, and the flame retardant agent,
wherein when the weight of the flame retardant
composition is set to 100 percent by weight, the mixing is performed so that the content of the fluorinated compound in the flame retardant composition is 0.1 to 1.0 percent by weight .
[12] The method for manufacturing a flame retardant
composition according to Claim 10 or 11,
wherein the mixing of the thermoplastic resin, the cellulose, the rubber having a siloxane bond, and the flame retardant agent is melt-kneading performed by a kneading machine .
[13] A method for manufacturing a molded article, the method comprising :
preparing a flame retardant composition; and
molding the flame retardant composition,
wherein the flame retardant composition is manufactured by the method for manufacturing a flame retardant
composition according to any one of Claims 10 to 12.
[14] The method for manufacturing a molded article according to Claim 13,
wherein the molding is extrusion molding or injection molding .
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP14816782.8A EP2989166B1 (en) | 2013-06-28 | 2014-06-19 | Flame retardant composition and molded article including the same |
CN201480034019.6A CN105308126B (en) | 2013-06-28 | 2014-06-19 | Flame-retardant composition and molded product including it |
US14/900,275 US20160369093A1 (en) | 2013-06-28 | 2014-06-19 | Flame retardant composition and molded article including the same |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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JP2013136156A JP6091358B2 (en) | 2013-06-28 | 2013-06-28 | Flame retardant composition and molded article having the same |
JP2013-136156 | 2013-06-28 |
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EP (1) | EP2989166B1 (en) |
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JP6399901B2 (en) * | 2013-11-26 | 2018-10-03 | キヤノン株式会社 | Flame retardant composition |
JP6425501B2 (en) * | 2013-11-28 | 2018-11-21 | キヤノン株式会社 | Flame retardant composition having polybutylene terephthalate |
CN106543634A (en) * | 2016-11-25 | 2017-03-29 | 西华大学 | A kind of flame-retardant ABS compound material and preparation method thereof |
WO2019124199A1 (en) * | 2017-12-22 | 2019-06-27 | ポリプラスチックス株式会社 | Thermoplastic resin composition |
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JP2015010154A (en) | 2015-01-19 |
EP2989166A1 (en) | 2016-03-02 |
CN105308126B (en) | 2019-02-26 |
EP2989166A4 (en) | 2016-11-30 |
US20160369093A1 (en) | 2016-12-22 |
CN105308126A (en) | 2016-02-03 |
EP2989166B1 (en) | 2018-08-08 |
JP6091358B2 (en) | 2017-03-08 |
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