KR20120072972A - 아크릴계 수지 조성물 및 이를 이용한 성형품 - Google Patents
아크릴계 수지 조성물 및 이를 이용한 성형품 Download PDFInfo
- Publication number
- KR20120072972A KR20120072972A KR1020100134928A KR20100134928A KR20120072972A KR 20120072972 A KR20120072972 A KR 20120072972A KR 1020100134928 A KR1020100134928 A KR 1020100134928A KR 20100134928 A KR20100134928 A KR 20100134928A KR 20120072972 A KR20120072972 A KR 20120072972A
- Authority
- KR
- South Korea
- Prior art keywords
- weight
- copolymer
- resin composition
- acrylic
- compound
- Prior art date
Links
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 title description 2
- 239000011342 resin composition Substances 0.000 title description 2
- -1 vinyl cyanide compound Chemical class 0.000 claims abstract description 99
- 229920006243 acrylic copolymer Polymers 0.000 claims abstract description 54
- 229920001577 copolymer Polymers 0.000 claims abstract description 53
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 44
- 239000000203 mixture Substances 0.000 claims abstract description 43
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 37
- 239000004925 Acrylic resin Substances 0.000 claims abstract description 36
- 229920000178 Acrylic resin Polymers 0.000 claims abstract description 36
- 239000002245 particle Substances 0.000 claims abstract description 20
- 239000011258 core-shell material Substances 0.000 claims abstract description 14
- 239000002356 single layer Substances 0.000 claims abstract description 12
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 32
- 239000010410 layer Substances 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 14
- 150000003440 styrenes Chemical class 0.000 claims description 14
- 125000005843 halogen group Chemical group 0.000 claims description 7
- VTPNYMSKBPZSTF-UHFFFAOYSA-N 1-ethenyl-2-ethylbenzene Chemical group CCC1=CC=CC=C1C=C VTPNYMSKBPZSTF-UHFFFAOYSA-N 0.000 claims description 6
- XHUZSRRCICJJCN-UHFFFAOYSA-N 1-ethenyl-3-ethylbenzene Chemical group CCC1=CC=CC(C=C)=C1 XHUZSRRCICJJCN-UHFFFAOYSA-N 0.000 claims description 6
- WHFHDVDXYKOSKI-UHFFFAOYSA-N 1-ethenyl-4-ethylbenzene Chemical group CCC1=CC=C(C=C)C=C1 WHFHDVDXYKOSKI-UHFFFAOYSA-N 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 abstract description 5
- 229920003023 plastic Polymers 0.000 abstract description 3
- 239000004033 plastic Substances 0.000 abstract description 3
- 239000002355 dual-layer Substances 0.000 abstract 2
- 230000000704 physical effect Effects 0.000 description 13
- 125000000217 alkyl group Chemical group 0.000 description 12
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 9
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 7
- 229920002877 acrylic styrene acrylonitrile Polymers 0.000 description 7
- 238000007720 emulsion polymerization reaction Methods 0.000 description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- TVONJMOVBKMLOM-UHFFFAOYSA-N 2-methylidenebutanenitrile Chemical compound CCC(=C)C#N TVONJMOVBKMLOM-UHFFFAOYSA-N 0.000 description 4
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 238000012662 bulk polymerization Methods 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 4
- 229920000578 graft copolymer Polymers 0.000 description 4
- 150000002391 heterocyclic compounds Chemical class 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 238000010557 suspension polymerization reaction Methods 0.000 description 4
- YAAQEISEHDUIFO-UHFFFAOYSA-N C=CC#N.OC(=O)C=CC=CC1=CC=CC=C1 Chemical compound C=CC#N.OC(=O)C=CC=CC1=CC=CC=C1 YAAQEISEHDUIFO-UHFFFAOYSA-N 0.000 description 3
- 239000004609 Impact Modifier Substances 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 230000003078 antioxidant effect Effects 0.000 description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
- 239000004926 polymethyl methacrylate Substances 0.000 description 3
- 229920000638 styrene acrylonitrile Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing 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
- 230000000996 additive effect Effects 0.000 description 2
- 125000005250 alkyl acrylate group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- WWPXOMXUMORZKI-UHFFFAOYSA-N butyl prop-2-enoate;prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1.CCCCOC(=O)C=C WWPXOMXUMORZKI-UHFFFAOYSA-N 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000002667 nucleating agent Substances 0.000 description 2
- UTOPWMOLSKOLTQ-UHFFFAOYSA-N octacosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O UTOPWMOLSKOLTQ-UHFFFAOYSA-N 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 230000000475 sunscreen effect Effects 0.000 description 2
- 239000000516 sunscreening agent Substances 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 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 description 1
- UWSMKYBKUPAEJQ-UHFFFAOYSA-N 5-Chloro-2-(3,5-di-tert-butyl-2-hydroxyphenyl)-2H-benzotriazole Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O UWSMKYBKUPAEJQ-UHFFFAOYSA-N 0.000 description 1
- 108700042658 GAP-43 Proteins 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- XITRBUPOXXBIJN-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1 XITRBUPOXXBIJN-UHFFFAOYSA-N 0.000 description 1
- 238000000071 blow moulding Methods 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- AYBQEWUIMBWDHL-UHFFFAOYSA-N buta-1,3-diene;methyl 2-methylprop-2-enoate;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N.COC(=O)C(C)=C AYBQEWUIMBWDHL-UHFFFAOYSA-N 0.000 description 1
- 125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 description 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 125000001072 heteroaryl group Chemical group 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 description 1
- 125000005638 hydrazono group Chemical group 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- DEAKWVKQKRNPHF-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;prop-2-enenitrile;styrene Chemical compound C=CC#N.COC(=O)C(C)=C.C=CC1=CC=CC=C1 DEAKWVKQKRNPHF-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 235000013872 montan acid ester Nutrition 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010558 suspension polymerization method Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000003856 thermoforming Methods 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 239000000326 ultraviolet stabilizing agent 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
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/08—Homopolymers or copolymers of acrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/18—Homopolymers or copolymers of nitriles
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L35/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L35/06—Copolymers with vinyl aromatic monomers
-
- 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
- C08L51/003—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 by reactions only involving unsaturated carbon-to-carbon bonds
-
- 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
- C08L51/04—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 rubbers
-
- 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
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)
- Laminated Bodies (AREA)
Abstract
Description
항목 | 실시예 | 비교예 | ||||||||||
1 | 2 | 3 | 4 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | ||
(A) 제1 아크릴계 공중합체(중량%) | 25 | 25 | 25 | 25 | 25 | 25 | 25 | 25 | 25 | 25 | 25 | |
(B) 제2 아크릴계 공중합체(중량%) | 15 | 15 | 15 | 15 | 15 | 15 | 15 | 15 | 15 | 15 | 15 | |
(C) 내열 공중합체(중량%) | 40 | 40 | 40 | 60 | 40 | 40 | 40 | 40 | 40 | - | 60 | |
(D) 폴리알킬(메타)아크릴레이트(중량부*) | (D-1) | 2 | 3 | 4 | 3 | - | - | - | - | - | - | - |
(D-2) | - | - | - | - | - | 4 | - | - | - | - | - | |
(D-3) | - | - | - | - | - | - | 4 | - | - | - | - | |
(E) SAN(중량%) | 20 | 20 | 20 | - | 20 | 20 | 20 | - | 10 | 60 | - | |
(F) MSAN(중량부*) | - | - | - | - | - | - | - | 20 | 10 | - | - | |
충격강도(kgf?cm/cm) | 16 | 16 | 16 | 16 | 16 | 16 | 12 | 12 | 13 | 16 | 12 | |
내후성 | ΔE | 2.2 | 2.0 | 1.7 | 1.9 | 6.3 | 5.9 | 6.1 | 3.8 | 4.6 | 6.8 | 5.5 |
Δb | 1.5 | 1.1 | 0.9 | 1.0 | 5.2 | 4.8 | 5.0 | 2.0 | 2.6 | 6.0 | 3.9 | |
광택도(%) | 38.9 | 42.7 | 45.8 | 43.6 | 1.3 | 8.5 | 7.7 | 22.7 | 16.9 | 0.9 | 6.7 | |
연필경도 | 2B | B | B | B | 4B | 2B | 3B | 2B | 2B | 4B | 4B | |
내열도(℃) | 104 | 104 | 104 | 105 | 104 | 104 | 100 | 103 | 103 | 98 | 106 |
Claims (10)
- (A) 이중층 고무를 포함하는 코어-쉘 구조의 제1 아크릴계 공중합체;
(B) 단일층 고무를 포함하는 코어-쉘 구조의 제2 아크릴계 공중합체;
(C) α-메틸 스티렌, 페닐 N-치환 말레이미드, 또는 이들의 조합을 포함하는 방향족 비닐 화합물과 시안화 비닐 화합물의 내열 공중합체; 및
(D) 20,000 내지 30,000 g/mol의 중량평균 분자량을 가진 폴리알킬(메타)아크릴레이트
를 포함하는 아크릴계 수지 조성물.
- 제1항에 있어서,
상기 아크릴계 수지 조성물은
상기 제1 아크릴계 공중합체(A) 10 내지 50 중량%;
상기 제2 아크릴계 공중합체(B) 10 내지 30 중량%;
상기 방향족 비닐 화합물과 시안화 비닐 화합물의 내열 공중합체(C) 30 내지 70 중량%; 및
상기 (A), (B) 및 (C) 성분의 총량 100 중량부에 대하여 상기 폴리알킬(메타)아크릴레이트(D) 2 내지 4 중량부
를 포함하는 것인 아크릴계 수지 조성물.
- 제1항에 있어서,
상기 이중층 고무는 0.1 내지 0.5 ㎛의 평균입경을 가지는 것인 아크릴계 수지 조성물.
- 제1항에 있어서,
상기 이중층 고무는 아크릴계 화합물과 방향족 비닐 화합물의 공중합체를 포함하는 내부층, 및 아크릴계 화합물을 포함하는 외부층을 포함하는 것인 아크릴계 수지 조성물.
- 제1항에 있어서,
상기 단일층 고무는 0.5 내지 1.0 ㎛의 평균입경을 가지는 제1 고무와, 0.1 내지 0.3 ㎛의 평균입경을 가지는 제2 고무를 포함하는 것인 아크릴계 수지 조성물.
- 제1항에 있어서,
상기 단일층 고무는 아크릴계 화합물을 포함하는 것인 아크릴계 수지 조성물.
- 제1항에 있어서,
상기 제1 아크릴계 공중합체(A)와 상기 제2 아크릴계 공중합체(B)는 80:20 내지 20:80의 중량비로 포함되는 것인 아크릴계 수지 조성물.
- 제1항에 있어서,
상기 폴리알킬(메타)아크릴레이트(D)는 상기 (A), (B) 및 (C) 성분의 총량 100 중량부에 대하여 2 내지 3 중량부로 포함되는 것인 아크릴계 수지 조성물.
- 제1항에 있어서,
상기 아크릴계 수지 조성물은 (E) 방향족 비닐 화합물과 시안화 비닐 화합물의 공중합체를 더 포함하고,
상기 방향족 비닐 화합물은 스티렌, o-에틸 스티렌, m-에틸 스티렌, p-에틸 스티렌, 할로겐 치환 스티렌, 또는 이들의 조합을 포함하는 것인 아크릴계 수지 조성물.
- 제1항 내지 제9항 중 어느 한 항의 아크릴계 수지 조성물을 이용하여 제조된 성형품.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020100134928A KR101466152B1 (ko) | 2010-12-24 | 2010-12-24 | 아크릴계 수지 조성물 및 이를 이용한 성형품 |
PCT/KR2011/006969 WO2012086901A1 (ko) | 2010-12-24 | 2011-09-21 | 아크릴계 수지 조성물 및 이를 이용한 성형품 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020100134928A KR101466152B1 (ko) | 2010-12-24 | 2010-12-24 | 아크릴계 수지 조성물 및 이를 이용한 성형품 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20120072972A true KR20120072972A (ko) | 2012-07-04 |
KR101466152B1 KR101466152B1 (ko) | 2014-11-27 |
Family
ID=46314144
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020100134928A KR101466152B1 (ko) | 2010-12-24 | 2010-12-24 | 아크릴계 수지 조성물 및 이를 이용한 성형품 |
Country Status (2)
Country | Link |
---|---|
KR (1) | KR101466152B1 (ko) |
WO (1) | WO2012086901A1 (ko) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9447275B2 (en) | 2013-09-03 | 2016-09-20 | Samsung Sdi Co., Ltd. | Molded article for automobile using thermoplastic resin composition |
KR20170057205A (ko) * | 2017-05-12 | 2017-05-24 | 롯데첨단소재(주) | 착색성 및 기계적 물성이 우수한 열가소성 수지 조성물 |
US9783668B2 (en) | 2013-06-28 | 2017-10-10 | Lotte Advanced Materials Co., Ltd. | Thermoplastic resin composition and molded article using the same |
KR20200055662A (ko) * | 2018-11-13 | 2020-05-21 | 주식회사 엘지화학 | 열가소성 수지 조성물 |
WO2020101326A1 (ko) * | 2018-11-13 | 2020-05-22 | 주식회사 엘지화학 | 열가소성 수지 조성물 |
WO2020101332A1 (ko) * | 2018-11-13 | 2020-05-22 | 주식회사 엘지화학 | 열가소성 수지 조성물 |
US11608401B2 (en) | 2018-10-31 | 2023-03-21 | Lg Chem, Ltd. | Thermoplastic resin composition |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3632938B1 (en) * | 2018-10-05 | 2023-05-03 | Trinseo Europe GmbH | Vinylidene substituted aromatic monomer and cyclic (meth)acrylate ester polymers |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU683128B2 (en) * | 1994-01-10 | 1997-10-30 | Umg Abs, Ltd. | Maleimide copolymer and resin composition containing the same |
KR100530567B1 (ko) * | 1999-02-04 | 2005-11-22 | 제일모직주식회사 | 내충격성이 우수한 열가소성 수지 조성물 |
KR100585942B1 (ko) * | 1999-06-24 | 2006-06-01 | 제일모직주식회사 | 내열성 및 신율특성이 우수한 열가소성 수지 조성물 |
KR100433572B1 (ko) * | 2001-10-23 | 2004-06-02 | 제일모직주식회사 | 표면광택, 내충격성 및 유동성이 우수한 열가소성 수지조성물 |
KR100497169B1 (ko) * | 2002-07-31 | 2005-06-23 | 주식회사 엘지화학 | 고무중합체의 제조방법 및 이를 포함하는 abs계 수지 |
KR100515592B1 (ko) * | 2003-06-18 | 2005-09-20 | 주식회사 엘지화학 | 열가소성 수지 조성물 |
EP1831306B1 (en) * | 2004-12-31 | 2010-12-29 | LG Chem, Ltd. | Plastic resin composition having improved heat resistance, weld strength, chemical resistance, impact strength and elongation |
KR100815995B1 (ko) * | 2006-06-08 | 2008-03-21 | 제일모직주식회사 | 저온 및 상온 내충격성과 착색성 및 내후성이 우수한asa 그라프트 공중합체 및 이를 포함한 열가소성 수지조성물 |
KR101211341B1 (ko) * | 2008-06-30 | 2012-12-11 | 주식회사 엘지화학 | 열가소성 수지 |
KR101151108B1 (ko) * | 2008-10-20 | 2012-06-01 | 주식회사 엘지화학 | 열가소성 수지 및 그 제조방법 |
-
2010
- 2010-12-24 KR KR1020100134928A patent/KR101466152B1/ko active IP Right Grant
-
2011
- 2011-09-21 WO PCT/KR2011/006969 patent/WO2012086901A1/ko active Application Filing
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9783668B2 (en) | 2013-06-28 | 2017-10-10 | Lotte Advanced Materials Co., Ltd. | Thermoplastic resin composition and molded article using the same |
US9447275B2 (en) | 2013-09-03 | 2016-09-20 | Samsung Sdi Co., Ltd. | Molded article for automobile using thermoplastic resin composition |
KR20170057205A (ko) * | 2017-05-12 | 2017-05-24 | 롯데첨단소재(주) | 착색성 및 기계적 물성이 우수한 열가소성 수지 조성물 |
US11608401B2 (en) | 2018-10-31 | 2023-03-21 | Lg Chem, Ltd. | Thermoplastic resin composition |
KR20200055662A (ko) * | 2018-11-13 | 2020-05-21 | 주식회사 엘지화학 | 열가소성 수지 조성물 |
WO2020101326A1 (ko) * | 2018-11-13 | 2020-05-22 | 주식회사 엘지화학 | 열가소성 수지 조성물 |
WO2020101332A1 (ko) * | 2018-11-13 | 2020-05-22 | 주식회사 엘지화학 | 열가소성 수지 조성물 |
JP2021523283A (ja) * | 2018-11-13 | 2021-09-02 | エルジー・ケム・リミテッド | 熱可塑性樹脂組成物 |
US11377547B2 (en) | 2018-11-13 | 2022-07-05 | Lg Chem, Ltd. | Thermoplastic resin composition |
US11499046B2 (en) | 2018-11-13 | 2022-11-15 | Lg Chem, Ltd. | Thermoplastic resin composition |
TWI828793B (zh) * | 2018-11-13 | 2024-01-11 | 南韓商Lg化學股份有限公司 | 熱塑性樹脂組成物 |
Also Published As
Publication number | Publication date |
---|---|
KR101466152B1 (ko) | 2014-11-27 |
WO2012086901A1 (ko) | 2012-06-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR101466152B1 (ko) | 아크릴계 수지 조성물 및 이를 이용한 성형품 | |
EP3219755B1 (en) | Thermoplastic resin composition and molded product produced therefrom | |
KR101681212B1 (ko) | 열가소성 수지 조성물을 이용한 자동차용 성형품 | |
KR101531613B1 (ko) | 열가소성 수지 조성물 및 이를 이용한 성형품 | |
US9422426B2 (en) | Transparent thermoplastic resin composition and molded article using the same | |
US9783668B2 (en) | Thermoplastic resin composition and molded article using the same | |
KR20140005510A (ko) | 열가소성 수지 조성물 및 이를 이용한 성형품 | |
KR101770454B1 (ko) | 열가소성 수지 조성물 및 이로부터 제조된 성형품 | |
KR101466151B1 (ko) | 아크릴계 수지 조성물 및 이를 이용한 성형품 | |
KR102396611B1 (ko) | 열가소성 수지 조성물 및 이를 이용한 성형품 | |
US11814513B2 (en) | Thermoplastic resin composition and molded product using same | |
KR101466148B1 (ko) | 아크릴계 열가소성 수지 조성물 및 이를 이용한 성형품 | |
KR101497131B1 (ko) | 아크릴계 열가소성 수지 조성물 및 이를 이용한 성형품 | |
KR101760976B1 (ko) | 열가소성 수지 조성물 및 이로부터 제조된 성형품 | |
KR102066598B1 (ko) | 열가소성 수지 조성물, 이의 제조방법 및 이를 포함하여 제조되는 성형품 | |
KR20240134842A (ko) | 열가소성 수지 조성물 및 이를 이용한 성형품 | |
KR102001485B1 (ko) | 열가소성 수지 조성물 및 이를 이용한 성형품 | |
KR102417772B1 (ko) | 열가소성 수지 조성물 및 이로부터 제조된 성형품 | |
KR102581489B1 (ko) | 열가소성 수지 조성물 및 이로부터 제조된 성형품 | |
KR20160035579A (ko) | 투명 열가소성 수지 조성물 및 이를 이용한 성형품 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 20101224 |
|
PG1501 | Laying open of application | ||
A201 | Request for examination | ||
PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20120806 Comment text: Request for Examination of Application Patent event code: PA02011R01I Patent event date: 20101224 Comment text: Patent Application |
|
E902 | Notification of reason for refusal | ||
PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20131017 Patent event code: PE09021S01D |
|
E902 | Notification of reason for refusal | ||
PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20140417 Patent event code: PE09021S01D |
|
E701 | Decision to grant or registration of patent right | ||
PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20141015 |
|
GRNT | Written decision to grant | ||
PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 20141121 Patent event code: PR07011E01D |
|
PR1002 | Payment of registration fee |
Payment date: 20141121 End annual number: 3 Start annual number: 1 |
|
PG1601 | Publication of registration | ||
FPAY | Annual fee payment |
Payment date: 20171011 Year of fee payment: 4 |
|
PR1001 | Payment of annual fee |
Payment date: 20171011 Start annual number: 4 End annual number: 4 |
|
FPAY | Annual fee payment |
Payment date: 20181008 Year of fee payment: 5 |
|
PR1001 | Payment of annual fee |
Payment date: 20181008 Start annual number: 5 End annual number: 5 |
|
FPAY | Annual fee payment |
Payment date: 20191008 Year of fee payment: 6 |
|
PR1001 | Payment of annual fee |
Payment date: 20191008 Start annual number: 6 End annual number: 6 |
|
PR1001 | Payment of annual fee |
Payment date: 20201006 Start annual number: 7 End annual number: 7 |
|
PR1001 | Payment of annual fee |
Payment date: 20231004 Start annual number: 10 End annual number: 10 |