WO2019190067A1 - Composition de résine thermoplastique et article moulé formé à partir de celle-ci - Google Patents
Composition de résine thermoplastique et article moulé formé à partir de celle-ci Download PDFInfo
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- WO2019190067A1 WO2019190067A1 PCT/KR2019/002537 KR2019002537W WO2019190067A1 WO 2019190067 A1 WO2019190067 A1 WO 2019190067A1 KR 2019002537 W KR2019002537 W KR 2019002537W WO 2019190067 A1 WO2019190067 A1 WO 2019190067A1
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- resin composition
- thermoplastic resin
- weight
- aromatic vinyl
- copolymer
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Classifications
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- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/101—Esters; Ether-esters of monocarboxylic acids
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/20—Carboxylic acid amides
-
- 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
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/12—Polyester-amides
Definitions
- the present invention relates to a thermoplastic resin composition and a molded article formed therefrom. More specifically, the present invention relates to a thermoplastic resin composition having excellent antistatic property, surface hydrophobicity, and the like, and a molded article formed therefrom.
- thermoplastic resin rubber-modified aromatic vinyl copolymer resins such as acrylonitrile-butadiene-styrene copolymer resin (ABS resin) are excellent in mechanical properties, processability, appearance characteristics, etc. It is widely used as interior / exterior materials for automobiles and exterior materials for construction.
- ABS resin acrylonitrile-butadiene-styrene copolymer resin
- the plastic products prepared from the conventional thermoplastic resin composition have little moisture absorbing power in the air and accumulate without generating the generated static electricity, dust in the air may be adsorbed, causing surface contamination and electrostatic shock, and malfunction of the device. This may cause a malfunction.
- an antistatic agent may be used, but in order to obtain appropriate antistatic property, an excessive amount of antistatic agent is required, and in this case, deterioration in compatibility, mechanical properties, etc. of the thermoplastic resin composition It may occur.
- the surface when the thermoplastic resin composition is applied to a product installed outdoors such as a building exterior material, the surface may be modified to have hydrophobicity in order to reduce contamination, dust adhesion due to precipitation, snowfall, and the like.
- thermoplastic resin composition In order to have a hydrophobic surface of the thermoplastic resin composition, a method such as adding a hydrophobic film coating or the like is used, but such a method has disadvantages such as an increase in cost and a decrease in productivity due to the addition of the process.
- a method of adding various additives capable of imparting hydrophobicity may be used, but conventionally used silica-based, fluorine-based, and ionic-based additives may cause problems such as deterioration in color, appearance, physical properties, etc. due to excessive addition. There is a risk of rising issues.
- thermoplastic resin compositions having excellent antistatic property, surface hydrophobicity, balance of physical properties thereof, and the like without these problems.
- Patent Publication No. 2014-0135790 discloses in, for example, Patent Publication No. 2014-0135790.
- An object of the present invention is to provide a thermoplastic resin composition excellent in antistatic property, surface hydrophobicity and the like.
- Another object of the present invention is to provide a molded article formed from the thermoplastic resin composition.
- thermoplastic resin composition may be a rubber-modified aromatic vinyl copolymer resin; Aliphatic polyamide resins; Polyetheresteramide block copolymers; Saturated fatty acid bis amide; And aliphatic carboxylic acid ester compounds.
- thermoplastic resin composition of embodiment 1, wherein the thermoplastic resin composition comprises about 60 to about 95 wt% of the rubber-modified aromatic vinyl copolymer resin and about 100 wt% of the base resin including about 5 to about 40 wt% of the aliphatic polyamide resin.
- the polyetheresteramide block copolymer To about 1 part by weight to about 15 parts by weight of the polyetheresteramide block copolymer, about 0.1 to about 5 parts by weight of the saturated fatty acid bisamide, and about 0.1 to about 10 parts by weight of the aliphatic carboxylic acid ester compound. Can be.
- the rubber modified aromatic vinyl copolymer resin may include a rubber modified vinyl graft copolymer and an aromatic vinyl copolymer resin.
- the rubber-modified vinyl graft copolymer may be a graft polymerized monomer mixture comprising an aromatic vinyl monomer and a vinyl cyanide monomer in the rubbery polymer.
- the polyetheresteramide block copolymer is an amino carboxylic acid, lactam or diamine-dicarboxylate having 6 or more carbon atoms; Polyalkylene glycols; And it may be a block copolymer of the reaction mixture comprising a dicarboxylic acid having 4 to 20 carbon atoms.
- the saturated fatty acid bis amide is one of methylene bis stearamide, methylene bis oleamide, ethylene bis stearamide, ethylene bis oleamide, hexamethylene bis stearamide and hexamethylene bis oleamide It may contain the above.
- the aliphatic carboxylic acid ester compound may be a dehydration product of an aliphatic carboxylic acid having 10 to 100 carbon atoms and a monovalent or polyhydric alcohol having 2 to 50 carbon atoms.
- the weight ratio of the saturated fatty acid bis amide and the aliphatic carboxylic acid ester compound may be about 1: 2 to about 1: 8.
- the thermoplastic resin composition may have a surface resistance value of about 1 ⁇ 10 9 to about 2 ⁇ 10 10 ⁇ / sq. Measured according to ASTM D257.
- the thermoplastic resin composition may have a half-life of about 0.1 seconds to about 2 seconds as measured according to KS K 0555.
- the thermoplastic resin composition may drop 3 ⁇ l of distilled water into a 100 mm ⁇ 100 mm size specimen, and the contact angle of the water droplet on the surface of the specimen measured by a contact angle measuring instrument may be about 92 to about 105 °. have.
- the molded article is formed from the thermoplastic resin composition according to any one of 1 to 11.
- This invention has the effect of the invention which provides the thermoplastic resin composition excellent in antistatic property, surface hydrophobicity, etc., and the molded article formed therefrom.
- thermoplastic resin composition is (A) rubber-modified aromatic vinyl copolymer resin; (B) aliphatic polyamide resins; (C) polyetheresteramide block copolymers; (D) saturated fatty acid bis amide; And (E) aliphatic carboxylic acid ester compounds.
- the rubber modified aromatic vinyl copolymer resin of the present invention may include (A1) rubber modified vinyl graft copolymer and (A2) aromatic vinyl copolymer resin.
- Rubber-modified vinyl graft copolymer according to an embodiment of the present invention may be a graft polymerized monomer mixture comprising an aromatic vinyl monomer and a vinyl cyanide monomer in the rubber polymer.
- the rubber-modified vinyl graft copolymer may be obtained by graft polymerization of a monomer mixture comprising an aromatic vinyl monomer and a vinyl cyanide monomer in a rubbery polymer, and, if necessary, processability and The monomer which gives heat resistance can be further included and graft-polymerized.
- the polymerization may be carried out by known polymerization methods such as emulsion polymerization and suspension polymerization.
- the rubber-modified vinyl graft copolymer may form a core (rubber polymer) -shell (copolymer of monomer mixture) structure, but is not limited thereto.
- the rubbery polymer may be a diene rubber such as polybutadiene, poly (styrene-butadiene), poly (acrylonitrile-butadiene), or a saturated rubber hydrogenated to the diene rubber, isoprene rubber, C 2 to C 10 alkyl (meth) acrylate rubbers, copolymers of alkyl (meth) acrylates having 2 to 10 carbon atoms and styrene, ethylene-propylene-diene monomer terpolymers (EPDM), and the like. These can be applied individually or in mixture of 2 or more types.
- a diene rubber, (meth) acrylate rubber, etc. can be used, Specifically, butadiene rubber, butyl acrylate rubber, etc. can be used.
- the rubbery polymer (rubber particles) has an average particle size (D50) measured by particle size analyzer of about 0.05 to about 6 ⁇ m, for example about 0.15 to about 4 ⁇ m, specifically about 0.25 to about 3.5 ⁇ m Can be.
- D50 average particle size measured by particle size analyzer of about 0.05 to about 6 ⁇ m, for example about 0.15 to about 4 ⁇ m, specifically about 0.25 to about 3.5 ⁇ m Can be.
- the thermoplastic resin composition may be excellent in impact resistance, appearance characteristics, and the like.
- the content of the rubbery polymer may be about 20 to about 70% by weight, for example about 25 to about 60% by weight of the total 100% by weight of the rubber-modified vinyl-based graft copolymer, the monomer mixture (aromatic The vinyl monomer and the vinyl cyanide monomer) may be about 30 to about 80 wt%, for example about 40 to about 75 wt%, of 100 wt% of the total rubber-modified vinyl graft copolymer.
- the thermoplastic resin composition may be excellent in impact resistance, appearance characteristics, and the like.
- the aromatic vinyl monomer may be graft copolymerized to the rubbery polymer, styrene, ⁇ -methylstyrene, ⁇ -methylstyrene, p-methylstyrene, pt-butylstyrene, ethyl styrene, vinyl xylene, Monochlorostyrene, dichlorostyrene, dibromostyrene, vinylnaphthalene, etc. can be illustrated. These may be used alone or in combination of two or more thereof.
- the aromatic vinyl monomer may be included in an amount of about 10 wt% to about 90 wt%, for example, about 40 wt% to about 90 wt% in 100 wt% of the monomer mixture. In the above range, the processability, impact resistance, and the like of the thermoplastic resin composition may be excellent.
- the vinyl cyanide monomer is copolymerizable with the aromatic vinyl system, and may include acrylonitrile, methacrylonitrile, ethacrylonitrile, phenylacrylonitrile, ⁇ -chloroacrylonitrile, fumaronitrile, and the like. It can be illustrated. These may be used alone or in combination of two or more thereof. For example, acrylonitrile, methacrylonitrile, etc. can be used.
- the content of the vinyl cyanide monomer may be about 10 wt% to about 90 wt%, for example about 10 wt% to about 60 wt%, in 100 wt% of the monomer mixture. In the above range, the thermoplastic resin composition may have excellent chemical resistance, mechanical properties, and the like.
- monomers for imparting processability and heat resistance may include, but are not limited to, (meth) acrylic acid, maleic anhydride, N-substituted maleimide, and the like.
- the content may be about 15% by weight or less, for example about 0.1 to about 10% by weight of 100% by weight of the monomer mixture. In the above range, processability and heat resistance can be imparted to the thermoplastic resin composition without deteriorating other physical properties.
- the rubber-modified vinyl graft copolymer is a copolymer in which a styrene monomer, which is an aromatic vinyl compound, and an acrylonitrile monomer, which is a vinyl cyanide compound, are grafted to a butadiene rubber polymer, and butyl acryl.
- An acrylate-styrene-acrylonitrile graft copolymer (g-ASA) which is a copolymer in which the styrene monomer which is an aromatic vinyl type compound, and the acrylonitrile monomer which is a vinyl cyanide compound is grafted to a latex rubbery polymer can be illustrated. have.
- the rubber-modified vinyl graft copolymer is about 10 to about 50 weight in 100% by weight of the total rubber-modified aromatic vinyl copolymer resin (rubber modified vinyl graft copolymer and aromatic vinyl copolymer copolymer resin) %, For example from about 25 to about 45% by weight.
- the impact resistance, fluidity (molding processability), appearance properties, balance of physical properties, and the like of the thermoplastic resin composition may be excellent.
- the aromatic vinyl copolymer resin according to one embodiment of the present invention may be an aromatic vinyl copolymer resin used in a conventional rubber-modified vinyl copolymer resin.
- the aromatic vinyl copolymer resin may be a polymer of a monomer mixture including an aromatic vinyl monomer and a monomer copolymerizable with the aromatic vinyl monomer.
- the aromatic vinyl copolymer resin may be obtained by mixing an aromatic vinyl monomer and a monomer copolymerizable with an aromatic vinyl monomer, and then polymerizing them, and the polymerization may be emulsion polymerization, suspension polymerization, bulk polymerization, or the like. It can be carried out by a known polymerization method of.
- the aromatic vinyl monomers include styrene, ⁇ -methylstyrene, ⁇ -methylstyrene, p-methylstyrene, pt-butylstyrene, ethyl styrene, vinyl xylene, monochlorostyrene, dichlorostyrene, dibromostyrene , Vinylnaphthalene and the like can be used. These can be applied individually or in mixture of 2 or more types.
- the content of the aromatic vinyl monomer may be about 20 to about 90 wt%, for example about 30 to about 80 wt%, of 100 wt% of the total aromatic vinyl copolymer resin. In the above range, the impact resistance, fluidity, and the like of the thermoplastic resin composition may be excellent.
- the monomer copolymerizable with the aromatic vinyl monomer may include at least one of a vinyl cyanide monomer and an alkyl (meth) acrylic monomer.
- a vinyl cyanide monomer and an alkyl (meth) acrylic monomer may be a vinyl cyanide monomer or a vinyl cyanide monomer and an alkyl (meth) acrylic monomer, specifically, a vinyl cyanide monomer and an alkyl (meth) acrylic monomer.
- examples of the vinyl cyanide monomer may include acrylonitrile, methacrylonitrile, ethacrylonitrile, phenylacrylonitrile, ⁇ -chloroacrylonitrile, fumaronitrile, and the like, but are not limited thereto. Do not. These may be used alone or in combination of two or more thereof. For example, acrylonitrile, methacrylonitrile, etc. can be used.
- examples of the alkyl (meth) acrylic monomer may include (meth) acrylic acid and / or alkyl (meth) acrylate having 1 to 10 carbon atoms. These may be used alone or in combination of two or more thereof. For example, methyl methacrylate, methyl acrylate, etc. can be used.
- the content of the vinyl cyanide monomer may be 100% by weight of the monomer copolymerizable with the aromatic vinyl monomer.
- the thermoplastic resin composition may have excellent transparency, heat resistance, processability, and the like.
- the content of the monomer copolymerizable with the aromatic vinyl monomer may be about 10 to about 80 wt%, for example about 20 to about 70 wt%, of 100 wt% of the total aromatic vinyl copolymer resin. In the above range, the impact resistance, fluidity, and the like of the thermoplastic resin composition may be excellent.
- the aromatic vinyl copolymer resin has a weight average molecular weight (Mw) of about 10,000 to about 300,000 g / mol, for example, about 15,000 to about 150,000 g / mol, as measured by gel permeation chromatography (GPC). Can be. In the above range, the mechanical strength, moldability, and the like of the thermoplastic resin composition may be excellent.
- the aromatic vinyl copolymer resin may be included in about 50 to about 90% by weight, for example about 55 to about 75% by weight of 100% by weight of the total rubber-modified aromatic vinyl copolymer resin.
- Impact resistance, fluidity (molding processability) and the like of the thermoplastic resin composition in the above range may be excellent.
- the rubber-modified aromatic vinyl copolymer resin (A) is about 60% by weight of 100% by weight of the base resin (A + B) including the rubber-modified aromatic vinyl copolymer resin and the aliphatic polyamide resin. To about 95 weight percent, such as about 65 to about 85 weight percent. In the above range, the mechanical properties, antistatic properties, surface hydrophobicity, etc. of the thermoplastic resin composition may be excellent.
- the aliphatic polyamide resin according to one embodiment of the present invention can improve the antistatic properties of the thermoplastic resin composition even when a small amount of the antistatic agent is used, and a conventional aliphatic polyamide resin can be used.
- the aliphatic polyamide resin can be polyamide 6, polyamide 11, polyamide 12, polyamide 4.6, polyamide 6.6, polyamide 6.10, combinations thereof, and the like.
- polyamide 6, polyamide 6.6 and the like can be used.
- the aliphatic polyamide resin has a relative viscosity (RV) of about 2.0 to about 3.5, such as about 2.3 to about 3.5, as measured by a Ubbelodhde viscometer in a sulfuric acid solution (96%) at 25 ° C. About 3.2. It may be excellent in the antistatic property, heat resistance and the like of the thermoplastic resin composition in the above range.
- the aliphatic polyamide resin (B) is about 5 to about 40 weight of 100% by weight of the total base resin (A + B) comprising the rubber-modified aromatic vinyl copolymer resin and the aliphatic polyamide resin %, For example from about 15 to about 35% by weight.
- the mechanical properties of the thermoplastic resin composition may be excellent in antistatic properties.
- Polyetheresteramide block copolymer according to an embodiment of the present invention is to improve the antistatic properties of the thermoplastic resin composition (test piece), etc., a polyetheresteramide block copolymer commonly used as an antistatic agent Aminocarboxylic acids, lactams or diamine-dicarboxylates having 6 or more carbon atoms; Polyalkylene glycols; And a block copolymer of a reaction mixture containing dicarboxylic acid having 4 to 20 carbon atoms.
- Aminocarboxylic acids such as acid, ⁇ -aminocapric acid, 1,1-aminoundecanoic acid, 1,2-aminododecanoic acid and the like
- Lactams such as caprolactam, enanthlactam, capryllactam, lauryl lactam and the like
- salts of diamines and dicarboxylic acids such as salts of hexamethylenediamine-adipic acid, salts of hexamethylenediamine-isophthalic acid, and the like.
- 1,2-aminododecanoic acid, caprolactam, salts of hexamethylenediamine-adipic acid 1,2-a
- the polyalkylene glycol may include polyethylene glycol, poly (1,2- and 1,3-propylene glycol), polytetramethylene glycol, polyhexamethylene glycol, a block of ethylene glycol and propylene glycol or random air.
- a copolymer, a copolymer of ethylene glycol and tetrahydrofuran, etc. can be illustrated.
- polyethylene glycol, a copolymer of ethylene glycol and propylene glycol, etc. can be used.
- examples of the dicarboxylic acid having 4 to 20 carbon atoms include terephthalic acid, 1,4-cyclohexacarboxylic acid, sebacic acid, adipic acid, dodecanoic acid, and the like.
- the bond of the amino carboxylic acid, lactam or diamine-dicarboxylic acid salt of 6 or more carbon atoms; and the polyalkylene glycol; may be an ester bond, the amino carboxylic acid, lactam or of 6 or more carbon atoms
- the combination of the diamine-dicarboxylic acid salt and the dicarboxylic acid having 4 to 20 carbon atoms may be an amide bond, and the combination of the polyalkylene glycol; and the dicarboxylic acid having 4 to 20 carbon atoms; It may be an ester bond.
- the polyetheresteramide block copolymer may be prepared by a known synthesis method, for example, according to the synthesis method disclosed in Japanese Patent Publication No. 56-045419 and Japanese Patent Publication No. 55-133424. Can be.
- the polyetheresteramide block copolymer can comprise about 10 to about 95 weight percent of the polyether-ester block. It may be excellent in the antistatic property, heat resistance and the like of the thermoplastic resin composition in the above range.
- the polyetheresteramide block copolymer may be included in an amount of about 1 to about 15 parts by weight, such as about 2 to about 10 parts by weight, based on about 100 parts by weight of the base resin (A + B). In the above range, the antistatic property, impact resistance (impact strength) and the like of the thermoplastic resin composition may be excellent.
- Saturated fatty acid bis amide according to one embodiment of the present invention together with the aliphatic carboxylic acid ester compound, can improve the surface hydrophobicity, mold release property, etc., without deterioration of the antistatic properties of the thermoplastic resin composition, and the like Bis amides can be used.
- the saturated fatty acid bisamide is methylene bis stearamide, methylene bis oleamide, ethylene bis stearamide, ethylene bis oleamide, Hexamethylene bis stearamide, hexamethylene bis oleamide, combinations thereof, and the like.
- the saturated fatty acid bis amide may be included from about 0.1 to about 5 parts by weight, for example from about 0.1 to about 2 parts by weight, based on about 100 parts by weight of the base resin (A + B). In the above range, the surface hydrophobicity, mold release property and the like of the thermoplastic resin composition may be excellent.
- the aliphatic carboxylic acid ester compound according to one embodiment of the present invention is capable of improving surface hydrophobicity, mold release property, and the like, together with a saturated fatty acid bis amide, without deterioration of antistatic properties of the thermoplastic resin composition, and having 10 to 100 carbon atoms. It may be a dehydration product of an aliphatic carboxylic acid of and a monovalent or polyhydric alcohol having 2 to 50 carbon atoms.
- aliphatic carboxylic acid ester compound pentaerythritol tetrastearate, glycerol monostearate, palmityl palmitate, stearyl stearate, or a combination thereof may be used.
- the aliphatic carboxylic acid ester compound may be included in about 0.1 to about 10 parts by weight, for example about 1 to about 7 parts by weight, based on about 100 parts by weight of the base resin (A + B). In the above range, the surface hydrophobicity, mold release property and the like of the thermoplastic resin composition may be excellent.
- the weight ratio (C: (D + E)) of the polyetheresteramide block copolymer (C) and the saturated fatty acid bis amide (D) and aliphatic carboxylic acid ester compound (E) is from about 1: 0.2 to About 1: 1, for example, about 1: 0.43 to about 1: 0.75.
- the thermoplastic resin composition may have better antistatic property, surface hydrophobicity, release property, and the like.
- the weight ratio (D: E) of the saturated fatty acid bis amide (D) and the aliphatic carboxylic acid ester compound (E) is about 1: 2 to about 1: 8, for example about 1: 2 to about 1: 6, specifically about 1: 3 to about 1: 5.
- the surface hydrophobicity, mold release property, and the like of the thermoplastic resin composition may be more excellent.
- the thermoplastic resin composition according to one embodiment of the present invention may further include an additive included in a conventional thermoplastic resin composition.
- the additives may include, but are not limited to, flame retardants, fillers, antioxidants, anti drip agents, lubricants, mold release agents, nucleating agents, stabilizers, pigments, dyes, mixtures thereof, and the like.
- the content may be about 0.001 to about 40 parts by weight, for example about 0.1 to about 10 parts by weight, based on about 100 parts by weight of the thermoplastic resin.
- thermoplastic resin composition according to an embodiment of the present invention may be in the form of pellets mixed with the components and melt-extruded at about 200 to about 280 ° C, for example, about 220 to about 250 ° C, using a conventional twin screw extruder. Can be.
- the thermoplastic resin composition has a surface resistance value measured in accordance with ASTM D257 of about 1 ⁇ 10 9 to about 2 ⁇ 10 10 ⁇ / sq. (Square), for example about 7 ⁇ 10 9 to about 1 X 10 10 ⁇ / sq.
- the thermoplastic resin composition may have a half-life of about 0.1 to about 2 seconds, for example about 0.5 to about 1 second, as measured by KS K 0555.
- the thermoplastic resin composition is prepared by dropping 3 ⁇ l of distilled water into a 100 mm ⁇ 100 mm size specimen based on a water drop shape analysis method, and then measuring the surface of the specimen by using a drop shape analyzer (DSA 100).
- the droplet contact angle of may be about 92 to about 105 degrees, for example about 95 to about 100 degrees.
- the molded article according to the present invention is formed from the thermoplastic resin composition.
- the thermoplastic resin composition may be prepared in a pellet form, and the prepared pellet may be manufactured into various molded products (products) through various molding methods such as injection molding, extrusion molding, vacuum molding, and casting molding. Such molding methods are well known by those skilled in the art. Since the molded article is excellent in antistatic property, surface hydrophobicity, mechanical properties, balance of these properties, etc., it is useful as interior / exterior materials, interior / exterior materials for automobiles, building exterior materials, etc. of electrical / electronic products.
- SAN resin (weight average molecular weight: 130,000 g / mol) polymerized with 75% by weight of styrene and 25% by weight of acrylonitrile was used.
- polyamide 6 manufactured by Kepitchemtech, product name: EN-300 was used as the aliphatic polyamide resin (B1).
- polyamide 6T (manufacturer: DuPont, product name: HTN 501) was used.
- PELECTRON AS (PA6-PEO, manufactured by Sanyo) was used.
- Ethylene bis stearamide (manufacturer: Shin-Won Chem, product name: HI-LUB B-50) was used.
- PP-PEO olefin antistatic agent manufactured by Sanyo, product name: UC.
- Example Comparative example One 2 3 4 One 2 3 4 (A) (% by weight) 85 85 70 70 70 70 70 70 (B1) (wt%) 15 15 30 30 - 30 30 30 (B2) (wt%) - - - - 30 - - - (C) (parts by weight) 8 8 8 8 8 - 8 (D) (parts by weight) 0.5 One 0.5 One One One 6 - (E) (parts by weight) 3 5 3 5 5 5 5 5 - 6 (F) (parts by weight) - - - - - 8 - - Surface resistance value ( ⁇ / sq.) 8 ⁇ 10 9 8 ⁇ 10 9 8 ⁇ 10 9 8 ⁇ 10 9 4 ⁇ 10 11 5 ⁇ 10 11 1 ⁇ 10 10 9 ⁇ 10 9 Half-life (seconds) 0.2 0.2 0.2 0.2 4 4 0.5 0.4 Contact angle (°) 98 103 97 98 105 88 85
- thermoplastic resin composition of the present invention is excellent in both antistatic property and surface hydrophobicity.
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Abstract
Une composition de résine thermoplastique de la présente invention comprend : une résine de copolymère à base de vinyle aromatique modifiée par du caoutchouc; une résine de polyamide aliphatique; un copolymère séquencé d'amide d'ester de polyéther; un bisamide d'acide gras saturé; et un composé ester d'acide carboxylique aliphatique. La composition de résine thermoplastique présente une excellente résistance statique, une hydrophobicité de surface et similaire.
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| KR10-2018-0035544 | 2018-03-28 | ||
| KR20180035544 | 2018-03-28 | ||
| KR1020180148463A KR102234039B1 (ko) | 2018-03-28 | 2018-11-27 | 열가소성 수지 조성물 및 이로부터 형성된 성형품 |
| KR10-2018-0148463 | 2018-11-27 |
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| KR20170133445A (ko) * | 2015-03-31 | 2017-12-05 | 가부시키가이샤 아데카 | 수지 첨가제 조성물 및 대전 방지성 열가소성 수지 조성물 |
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2019
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| KR980009374A (ko) * | 1996-07-18 | 1998-04-30 | 유현식 | 영구적 대전방지성을 갖는 열가소성 스티렌계 수지 조성물 및 그 제조방법 |
| KR101276430B1 (ko) * | 2009-12-29 | 2013-06-19 | 주식회사 삼양사 | 열가소성 수지 조성물 |
| JP2011218642A (ja) * | 2010-04-08 | 2011-11-04 | Denki Kagaku Kogyo Kk | 帯電防止性能を有する多層成形体 |
| KR20170039197A (ko) * | 2014-08-06 | 2017-04-10 | 도레이 카부시키가이샤 | 섬유 강화 열가소성 수지 성형 재료 및 섬유 강화 열가소성 수지 성형품 |
| KR20170133445A (ko) * | 2015-03-31 | 2017-12-05 | 가부시키가이샤 아데카 | 수지 첨가제 조성물 및 대전 방지성 열가소성 수지 조성물 |
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