WO2014035055A1 - 아크릴로니트릴-아크릴레이트-스티렌 그라프트 공중합체 및 이를 포함하는 열가소성 수지 조성물 - Google Patents
아크릴로니트릴-아크릴레이트-스티렌 그라프트 공중합체 및 이를 포함하는 열가소성 수지 조성물 Download PDFInfo
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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
- 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
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F285/00—Macromolecular compounds obtained by polymerising monomers on to preformed graft polymers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F291/00—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00
- C08F291/12—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00 on to nitrogen-containing macromolecules
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/08—Copolymers of styrene
- C08L25/12—Copolymers of styrene with unsaturated nitriles
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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
- 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
- C08L51/06—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 homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1804—C4-(meth)acrylate, e.g. butyl (meth)acrylate, isobutyl (meth)acrylate or tert-butyl (meth)acrylate
Definitions
- the present invention relates to an acrylonitrile-acrylate-styrene graft copolymer and a thermoplastic resin composition comprising the same, and more particularly, an acrylic having a refractive index difference in which a rubber morphology is controlled, and in consideration of a refractive index of a target matrix polymer. It relates to a ronitrile-acrylate-styrene graft copolymer and a thermoplastic resin composition having excellent impact and weather resistance and excellent appearance characteristics.
- ABS resin is an acrylonitrile-butadiene-styrene terpolymer and has excellent impact resistance, rigidity, chemical resistance, and processability, and is widely used in various fields such as electric and electronic, construction, and automobile.
- ABS resin has a problem in that it is not suitable as an outdoor material because of poor weather resistance by using butadiene polymer as a rubber.
- thermoplastic resins excellent in weatherability and aging resistance are ASA resins (acrylonitrile-styrene-acrylate terpolymers) using crosslinked alkyl acrylate rubber polymers that have proven to be suitable.
- ASA resin has excellent weather resistance and aging resistance, and is used in various fields such as automobiles, ships, leisure products, building materials, and gardening.
- ASA polymers with excellent weatherability and aging resistance is disclosed in German Patent No. 1,260,135, wherein the core used is a large diameter latex of crosslinked acrylate having an average particle diameter of 150 to 800 nm and a narrow particle size distribution.
- the core used is a large diameter latex of crosslinked acrylate having an average particle diameter of 150 to 800 nm and a narrow particle size distribution.
- polymers comprising large diameter polyacrylate latex have improved notch impact strength, greater hardness and reduced shrinkage.
- large diameter acrylonitrile-acrylate-styrene graft copolymers have a disadvantage in that coloring is difficult compared to small diameter acrylonitrile-acrylate-styrene graft copolymers.
- materials known to date have excellent weather resistance and mechanical properties and have improved colorability.
- the coloring improvement effect of these materials is still insufficient due to the mixed use of a large diameter acrylonitrile-acrylate-styrene graft copolymer which lowers the coloring.
- These materials used alkyl acrylate polymers crosslinked with rubber components, and the refractive index of the alkyl acrylate was too low in comparison with styrene and acrylonitrile, so that a very vivid color could not be realized in coloring.
- An object of the present invention is to control the morphology of the rubber, and in addition to acrylonitrile-acrylate-styrene graft copolymer having a refractive index difference in consideration of the refractive index of the target matrix polymer, and excellent impact and weather resistance including the same, but also excellent in appearance characteristics It is to provide a thermoplastic resin composition.
- the present invention is an acrylonitrile-acrylate-styrene graft copolymer composition
- Seeds comprising at least one compound of an aromatic vinyl compound, a vinylcyan compound, and an alkyl (meth) acrylate compound; A rubber core surrounding the seed and comprising an alkyl acrylate; And a graft copolymer and a matrix polymer including a shell surrounding the core and including at least one of an aromatic vinyl compound, a vinyl cyan compound, and an alkyl (meth) acrylate compound.
- the morphology of satisfies the following Equations 1 and 2 at the same time,
- Refractive index of the oxide and the shell is a matrix, the refractive index of the polymer ( ⁇ D 25) and are each less than 0.035, a difference of 0.03 or less, or 0.02 or less, the refractive index of the core is the difference between the refractive index of the matrix polymer ( ⁇ D 25) 0.056 Exceeding, 0.08 or more, or 0.1 or more.
- Equation 1 may be, for example, 150 ⁇ 2 * r2 ⁇ 370, 150 ⁇ 2 * r2 ⁇ 350 or 200 ⁇ 2 * r2 ⁇ 300.
- Equation 2 may be, for example, 10 ⁇ r2-r1 ⁇ 70, 20 ⁇ r2-r1 ⁇ 50, or 20 ⁇ r2-r1 ⁇ 40.
- the present invention is an ASA (acrylonitrile-acrylate-styrene) -based graft copolymer composition, wherein the acrylonitrile-acrylate-styrene graft copolymer and the matrix polymer are 10:90 to 90:10. , 10:90 to 60:40, or 15:85 to 50:50.
- ASA acrylonitrile-acrylate-styrene
- the matrix polymer may be, for example, at least one selected from polymers including at least one compound of an aromatic vinyl compound, a vinyl cyan compound, and an alkyl (meth) acrylate compound.
- the present invention is a molded article
- the rubber morphology is controlled, and in addition to maintaining the existing impact properties in consideration of the refractive index of the target matrix polymer, the seed refractive index is prepared close to the refractive index of the target matrix polymer, so as not to reduce the colorability, the core having a large difference in refractive index
- the thickness and refractive index of the seed and the core are controlled to adjust the morphology of the chromium to improve the colorability to provide an acrylonitrile-acrylate-styrene graft copolymer having excellent appearance characteristics.
- the acrylonitrile-acrylate-styrene graft copolymer provided in the present invention includes, for example, a seed comprising at least one compound of an aromatic vinyl compound, a vinyl cyan compound, and an alkyl (meth) acrylate compound; A rubber core surrounding the seed and comprising an alkyl acrylate; And a shell surrounding the core, the shell including at least one compound of an aromatic vinyl compound, a vinyl cyan compound, and an alkyl (meth) acrylate compound.
- Seeds, cores and shells constituting the acrylonitrile-acrylate-styrene graft copolymer are, for example, in the range of 5 to 40: 20 to 60: 20 to 60, or 10 to 35: 30 to 55:30 It is especially preferable to be in the range of 50 to improve colorability while maintaining a moderate impact.
- the rubber content decreases, so that the impact reinforcing effect may be reduced as a graft copolymer. If the content exceeds the above range, the rubber content may fall and the rubber may aggregate together when the shell content falls. As a result, the compatibility with the resin may be significantly lowered, and thus the desired refractive index may not be obtained with the reduction of the impact reinforcing effect.
- the rubber content is lowered, the impact is reduced, and when the content of the alkyl acrylate is excessive, the content of the shell is lowered, the rubber is agglomerated and impacted by the reduction of resin compatibility The reinforcing effect is lowered and the refractive index is lowered.
- alkyl acrylate included in the core for example, methyl acrylate, ethyl acrylate, propyl acrylate, butyl acrylate, hexyl acrylate, octyl acrylate or 2-ethylhexyl acrylate may be used. N-butyl acrylate or 2-ethylhexyl acrylate can be used.
- the core of the rubber component may be, for example, a polymerized acrylic rubber including an alkyl acrylate and a crosslinking agent, and the gel content may be controlled when the crosslinking agent is included, and the rigidity is excellent.
- the average particle diameter to the core is, for example, more than 0.14 ⁇ m to less than 0.38 ⁇ m, 0.15 to 0.37 ⁇ m, 0.15 to 0.35 ⁇ m, or 0.2 to 0.3 ⁇ m, which is preferable for maintaining impact resistance and colorability balance.
- the aromatic vinyl compound that can be used for the seed and the shell may be at least one selected from the group consisting of styrene monomer derivatives of styrene, ⁇ -styrene, p-styrene and vinyl toluene, for example.
- the vinylcyan compound that may be used in the seed and the shell may be, for example, acrylonitrile, methacrylonitrile, or a mixture thereof.
- alkyl (meth) acrylate compounds that can be used in the seeds and shells are, for example, methyl acrylate, ethyl acrylate, propyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, methyl methacrylate, ethyl methacrylate. It may be at least one selected from the group consisting of late propyl methacrylate, 2-ethylhexyl methacrylate, methyl acrylate and ethyl acrylate.
- the seed, the core or both may be made by further including at least one compound represented by the following formula (1) as a crosslinking agent.
- A is independently a substituent or a (meth) acrylate group having a vinyl group
- a ' is a hydrogen group, a substituent having a vinyl group, an alkyl group having 1 to 30 carbon atoms or an arylalkyl group having 5 to 24 carbon atoms, or 5 carbon atoms It is an arylamine group of 24 to 24, or an aryl group of 6 to 30 carbon atoms,
- R is independently a divalent ethyl group or a propyl group, n is an integer from 0 to 15, 0 to 5, or 0 to 4).
- the seeds, cores or both are crosslinking agents such as divinylbenzene, 1,3-butanediol diacrylate, 1,3-butanediol dimethacrylate, 1,4-butanediol diacrylate, 1,4- Butanediol dimethacrylate, aryl acrylate, aryl methacrylate, trimethylolpropane triacrylate, tetraethylene glycol diacrylate, ethylene glycol dimethacrylate, diethylene glycol dimethacrylate, triethylene glycol dimethacryl It may further comprise one or more from the group consisting of latex, neopentyl glycol dimethacrylate, triallyl isocyanurate, triarylamine, and diallylamine.
- crosslinking agents such as divinylbenzene, 1,3-butanediol diacrylate, 1,3-butanediol dimethacrylate, 1,4-butanediol diacryl
- the crosslinking agent may be used in an amount of 0.01 to 5 parts by weight based on 100 parts by weight of the total monomers used in the preparation of the ASA graft copolymer, and in another example, 0.1 to 3 parts by weight.
- the shell may be included in an amount of 20 to 60 parts by weight based on a total of 100 parts by weight of the monomer forming the acrylonitrile-acrylate-styrene graft copolymer, for example.
- the content of the shell is small, the graft efficiency is reduced and the rubber is agglomerated to reduce the impact reinforcement effect due to the reduction of compatibility with the resin.
- the impact efficiency is decreased due to the reduction of the relative rubber content.
- the shell is, for example, a copolymer formed by graft polymerization including one or more selected from the group consisting of alkyl methacrylates, aromatic vinyl compounds and vinyl cyan compounds in order to control polymerization reactivity and refractive index to an appropriate level. .
- the shell is formed by graft polymerization with a copolymer comprising an aromatic vinyl compound and a vinyl cyan compound, or an aromatic vinyl compound, a vinyl cyan compound and an alkyl methacrylate.
- the final gel content of the graft copolymer is, for example, less than 92%, less than 90%, or 30 to 90%, and the graft rate is, for example, more than 20%, at least 25%, 25 to 100%, or 25 to 80%. It may be.
- the gel content is within the above range, the rigidity is excellent, and when the graft ratio is within the above range, the cohesive property is improved, which is advantageous for dispersion.
- the present invention is characterized in that the morphology of the rubber core satisfies the following Equations 1 and 2 simultaneously.
- the r1 is, for example, the radius of the seed, or the average radius, which means half of the seed particle size or the average particle diameter.
- the r2 is, for example, the radius of the core including the seed, or the average radius, which means 1/2 of the particle diameter or the average particle diameter of the core including the seed.
- the matrix polymer usable may be at least one selected from matrix polymers comprising at least one of aromatic vinyl compounds, vinyl cyan compounds and alkyl (meth) acrylate compounds.
- the matrix polymer may be, for example, a hard matrix resin.
- the hard matrix resin means a resin made of a hard polymer-forming monomer having a glass transition temperature of at least 80 ° C. or higher, or 80 to 200 ° C.
- the matrix polymer may be a SAN (styrene-acrylonitrile) resin.
- the refractive index of the refractive index of the oxide and the shell is preferred when it is less than the difference between the refractive index of the matrix polymer ( ⁇ D 25) 0.035, 0.03 or less, or 0.03 of less than considering the colored side to give transparency to the graft copolymer .
- the refractive index of the core is greater than 0.056, 0.08 or more, 0.06 to 0.15, or 0.08 to 0.13, which is different from the refractive index of the matrix polymer ( ⁇ D 25 ), so that the effect of improving colorability is remarkable and the refractive index is reduced to lower the refractive index difference.
- this relatively high butadiene or styrene is used for the core, the weather resistance and the impact strength are lowered, respectively.
- the ASA graft copolymer composition according to the present invention is an acrylonitrile-acrylate-styrene graft copolymer and one of an aromatic vinyl compound, a vinyl cyan compound, and an alkyl (meth) acrylate compound as a thermoplastic matrix resin. It is preferable to include at least one selected from hard matrix resins including at least one species in a weight ratio of 10:90 to 90:10.
- the acrylonitrile-acrylate-styrene graft copolymer can be prepared according to methods well known in the art such as, for example, emulsion polymerization.
- the acrylonitrile-acrylate-styrene graft copolymer may be prepared through the following three steps.
- the content of the monomers and the like used is based on 100 parts by weight of the total monomers used to prepare the acrylonitrile-styrene-acrylate copolymer.
- a seed is prepared by polymerizing 4 to 30 parts by weight of one or more monomers or monomer mixtures selected from the group consisting of aromatic vinyl compounds, vinyl cyan compounds and alkyl acrylates as a first step.
- the electrolyte may include 0.001 to 1 part by weight, a crosslinking agent of 0.01 to 3 parts by weight, an initiator of 0.01 to 3 parts by weight, and an emulsifier of 0.01 to 5 parts by weight.
- a core is then prepared by polymerizing a monomer mixture comprising 20 to 80 parts by weight of alkyl acrylate monomer and 0.01 to 3 parts by weight of crosslinking agent in the presence of the seed as a second step.
- the initiator may include 0.01 to 3 parts by weight and an emulsifier 0.01 to 5 parts by weight.
- the graft shell is then prepared by polymerizing 10 to 70 parts by weight of at least one monomer or monomer mixture selected from the group consisting of aromatic vinyl compounds and vinylcyan compounds in the presence of the rubber core as a third step.
- the initiator may include 0.01 to 3 parts by weight, a molecular weight regulator 0 to 3 parts by weight and an emulsifier 0.01 to 5 parts by weight.
- thermoplastic resin composition according to the present invention may be, for example, at least one selected from the group consisting of flame retardants, lubricants, antibacterial agents, mold release agents, nucleating agents, plasticizers, thermal stabilizers, antioxidants, light stabilizers, UV stabilizers, compatibilizers, pigments, dyes, and inorganic additives.
- the additive may further comprise 0.1 to 10 parts by weight based on a total of 100 parts by weight of the ASA graft polymer and the matrix resin.
- the thermoplastic resin composition may contain 0.1 to 5 weights of one or more additives selected from the group consisting of lubricants, antioxidants, UV stabilizers, pigments, and inorganic additives, based on 100 parts by weight of the total ASA graft polymer and the matrix resin. Parts, or 0.1 to 3 parts by weight may be further included.
- Molded articles prepared from such ASA-based graft copolymer composition is characterized in that the impact properties, weather resistance and colorability and gloss is improved to improve the appearance characteristics, but is not limited to, automotive parts, electrical / electronic components or It can be used for building materials.
- the acrylonitrile-acrylate-styrene graft copolymer is prepared in which the refractive index of the seed is made close to the refractive index of the target matrix while maintaining the existing impact properties in consideration of the refractive index of the target matrix polymer, thereby reducing colorability.
- the morphology of the core having a large difference in refractive index from the target matrix it is excellent in appearance characteristics when applied to the thermoplastic resin composition.
- thermoplastic resin composition 20% by weight of styrene, 45% by weight of butyl acrylate, and 35% by weight of chloro-acrylonitrile (26.25% by weight SM, 8.75% by weight AN), with r1 of 75 nm and r2 of 115 nm.
- Phosphorus acrylonitrile-acrylate-styrene graft copolymer 40 parts by weight and styrene-acrylonitrile copolymer 60 parts by weight (SM 45 parts by weight, AN 15 parts by weight, refractive index 1.573), lubricant 1 part by weight, antioxidant 0.5 weight part and 0.5 weight part of ultraviolet stabilizers were mixed, and the thermoplastic resin composition was prepared.
- the difference in refractive index between the seed, shell and matrix of the acrylonitrile-acrylate-styrene graft copolymer is ⁇ 0.02
- the difference in refractive index between the core and the matrix is 0.11
- the acrylonitrile-acrylate-styrene graft air The gel content of the coalescence is ⁇ 90%, the graft rate is characterized in that 35%.
- r1 and r2 were able to obtain a desired value by controlling the emulsifier content during polymerization
- SM is styrene monomer
- AN is acrylonitrile monomer
- MMA is methyl methacrylate
- BA is butyl acrylate.
- 2-EHA means 2-ethylhexyl acrylate.
- Example 1 consists of 10% by weight of styrene, 55% by weight of butyl acrylate, and 35% by weight of chloro-acrylonitrile (26.25% by weight SM, 8.75% by weight AN), r1 is 35 nm
- a thermoplastic resin composition was prepared in the same manner except that r 2 was 75 nm. At this time, the refractive index difference, the gel content and the graft ratio are the same as in Example 1.
- Example 1 consists of 25% by weight of seed styrene, 45% by weight of butyl acrylate as core, and 30% by weight of chloro-acrylonitrile (SM 22.5% by weight, 7.5% by AN), r1 is 110 nm
- a thermoplastic resin composition was prepared in the same manner except that r2 was 150 nm and the graft ratio was 28%. The refractive index difference and gel content at this time are the same as in Example 1.
- Example 1 it consisted of 30% by weight of seed styrene, 40% by weight of butyl acrylate, and 30% by weight of chloro-acrylonitrile (SM 22.5%, AN 7.5% by weight), r1 is 135 nm A thermoplastic resin composition was prepared in the same manner except that r2 was 175 nm and the graft rate was 25%. The refractive index difference and gel content at this time are the same as in Example 1.
- Example 1 consists of 25% by weight of styrene styrene, 45% by weight of butyl acrylate, and 30% by weight of chloro-acrylonitrile (22.5 parts by weight of SM, 7.5 parts by weight of AN), r1 is 80 nm and r2
- the thermoplastic resin composition was prepared in the same manner except for 110 nm, the graft ratio of 28%, and the gel content of 90%. The difference in refractive index at this time is the same as in Example 1.
- Example 1 consists of 25% by weight of styrene styrene, 35% by weight of butyl acrylate, and 40% by weight of chloro-acrylonitrile (30% by weight SM, 10% by weight AN), r1 is 100 nm
- a thermoplastic resin composition was prepared in the same manner except that r2 was 130 nm, the graft ratio was 40%, and the gel content was 85%. The difference in refractive index at this time is the same as in Example 1.
- Example 1 consists of 15% by weight of styrene, 45% by weight of butyl acrylate, and 40% by weight of chloro-acrylonitrile (30% by weight of SM, 10% by weight of AN), r1 is 70 nm
- a thermoplastic resin composition was prepared in the same manner except that r2 was 120 nm and the graft ratio was 45%.
- the refractive index difference and gel content at this time are the same as in Example 1.
- Example 1 it consists of 20% by weight of styrene, 45% by weight of butyl acrylate, and 35% by weight of chloro-acrylonitrile (SM 26.25%, AN 8.75% by weight), r1 is 100 nm A thermoplastic resin composition was prepared in the same manner except that r2 was 150 nm. At this time, the refractive index difference, the gel content and the graft ratio are the same as in Example 1.
- Example 1 consists of 25% by weight of styrene styrene, 30% by weight of butyl acrylate and 45% by weight of chloro-acrylonitrile (33.75% by SM, 11.25% by AN), with r1 of 90 nm
- a thermoplastic resin composition was prepared in the same manner except that r2 was 110 nm, the graft ratio was 45%, and the gel content was 80%.
- the refractive index difference and gel content at this time are the same as in Example 1.
- Example 1 consists of 35% by weight of seed styrene, 30% by weight of butyl acrylate as core, and 35% by weight of chloro-acrylonitrile (SM 26.25% by weight, AN 8.75% by weight), r1 is 115 nm
- a thermoplastic resin composition was prepared in the same manner except that r 2 was 135 nm. At this time, the refractive index difference, the gel content and the graft ratio are the same as in Example 1.
- the seed composition in Example 1 was styrene-acrylonitrile-methylmethacrylate (SM 15 wt%, AN 2 wt%, MMA 3 wt%) and the seed and matrix of acrylonitrile-acrylate-styrene graft copolymer A thermoplastic resin composition was prepared in the same manner except that the difference in refractive index between and was ⁇ 0.03. The gel content and graft rate at this time were the same as in Example 1.
- Example 1 Except that the seed composition in Example 1 is styrene-butyl acrylate (SM 15% by weight, BA 5% by weight) and the refractive index difference between the matrix and the seed of the acrylonitrile-acrylate-styrene graft copolymer is ⁇ 0.03. And to prepare a thermoplastic resin composition in the same manner. The gel content and graft rate at this time were the same as in Example 1.
- Example 1 Except that the seed composition in Example 1 is styrene-acrylonitrile (SM 15 wt%, AN 5 wt%) and the refractive index difference between the matrix and the seed of the acrylonitrile-acrylate-styrene graft copolymer is ⁇ 0.02. And to prepare a thermoplastic resin composition in the same manner. The gel content and graft rate at this time were the same as in Example 1.
- Seed composition in Example 1 is styrene-acrylonitrile-butyl acrylate (SM 12 wt.%, BA 4 wt.%, AN 4 wt.%), Seed and matrix of acrylonitrile-acrylate-styrene graft copolymer.
- a thermoplastic resin composition was prepared in the same manner except that the difference in refractive index between and was ⁇ 0.03. The gel content and graft rate at this time were the same as in Example 1.
- Example 1 the core composition is butyl acrylate-2-ethylhexyl acrylate (BA 25 wt%, 2-EHA 20 wt%), and the core of the acrylonitrile-acrylate-styrene graft copolymer with the matrix
- a thermoplastic resin composition was prepared in the same manner except that the difference in refractive index was 0.115.
- the gel content and graft rate at this time were the same as in Example 1.
- Example 1 the shell composition is styrene-acrylonitrile-methyl methacrylate (SM 26.25 wt%, AN 3.5 wt%, MMA 5.25 wt%) and the shell of acrylonitrile-acrylate-styrene graft copolymer
- SM 26.25 wt%, AN 3.5 wt%, MMA 5.25 wt% styrene-acrylonitrile-methyl methacrylate
- MMA 5.25 wt% styrene-acrylonitrile-methyl methacrylate
- a thermoplastic resin composition was prepared in the same manner except that the refractive index difference from the matrix was ⁇ 0.03.
- the gel content and graft rate at this time were the same as in Example 1.
- Example 1 4% by weight of styrene, 55% by weight of butyl acrylate, and 41% by weight of chloro-acrylonitrile (30.75% by weight SM, 10.25% by weight AN), r1 is 55 nm; A thermoplastic resin composition was prepared in the same manner except r2 was 135 nm and the graft ratio was 45%. The refractive index difference and gel content at this time are the same as in Example 1.
- Example 1 it consisted of 30% by weight of seed styrene, 40% by weight of butyl acrylate, and 30% by weight of chloro-acrylonitrile (SM 22.5%, AN 7.5% by weight), r1 is 50 nm. r2 was 70 nm and the thermoplastic resin composition was prepared in the same manner except that the graft ratio was 28%. The refractive index difference and gel content at this time are the same as in Example 1.
- Example 1 it consists of 30% by weight of seed styrene, 40% by weight of butyl acrylate and 30% by weight of chloro-acrylonitrile (22.5% by weight, 7.5% by weight AN), r1 is 145 nm. r2 is 190 nm, and the thermoplastic resin composition was prepared in the same manner except that the graft ratio was 28%. The refractive index difference and gel content at this time are the same as in Example 1.
- Example 1 consists of 10% by weight of styrene, 55% by weight of butyl acrylate, and 35% by weight of chloro-acrylonitrile (SM 26.25%, AN 8.75% by weight), r1 is 100 nm A thermoplastic resin composition was prepared in the same manner except r2 was 190 nm and the graft ratio was 35%. The refractive index difference and gel content at this time are the same as in Example 1.
- Example 1 consists of 10% by weight butyl acrylate, 50% by weight butyl acrylate and 40% by weight chloro-acrylonitrile (30% by weight SM, 10% by weight AN), r1 is 75 nm And r2 was 115 nm, except that the difference between the seed and the matrix refractive index was> 0.035 and the graft rate was 40%.
- the refractive index difference and gel content at this time are the same as in Example 1.
- Example 1 the seed composition was styrene-acrylonitrile-methyl methacrylate (SM 7 wt%, AN 3 wt%, MMA 10 wt%) and the seed of acrylonitrile-acrylate-styrene graft copolymer A thermoplastic resin composition was prepared in the same manner except that the refractive index difference from the matrix was 0.04. The gel content and graft rate at this time were the same as in Example 1.
- Example 1 the seed composition was styrene-butyl acrylate (SM 9 wt%, BA 11 wt%), except that the refractive index difference between the seed and the matrix of the acrylonitrile-acrylate-styrene graft copolymer was 0.05. And to prepare a thermoplastic resin composition in the same manner. The gel content and graft rate at this time were the same as in Example 1.
- the seed composition in Example 1 was styrene-acrylonitrile-butyl acrylate (SM 8% by weight, AN 4% by weight, BA 8% by weight) and the seed and matrix of acrylonitrile-acrylate-styrene graft copolymer Except that the refractive index difference between and 0.05 was prepared in the same manner as the thermoplastic resin composition.
- the gel content and graft rate at this time were the same as in Example 1.
- Example 1 Except that the core composition in Example 1 is butyl acrylate-styrene (SM 9 wt%, BA 11 wt%) and the refractive index difference between the core and the matrix of the acrylonitrile-acrylate-styrene graft copolymer is 0.05 And to prepare a thermoplastic resin composition in the same manner. The gel content and graft rate at this time were the same as in Example 1.
- thermoplastic resin composition was manufactured in the same manner as in Example 1, except that the core composition was butyl butadiene, and the refractive index difference between the core and the matrix of the acrylonitrile-acrylate-styrene graft copolymer was 0.056. At this time, the gel content was 94%, and the graft rate was 45%.
- thermoplastic resin composition and the like were evaluated for physical properties through the following methods:
- Refractive index The powder was compressed and measured with a refractometer (Metricon 2010).
- r1 was measured by dividing the average seed particle size in half
- r2 was measured by dividing the average particle diameter of the seed-containing core in half.
- Resin colorability 1 wt% carbon black was added during resin processing, and the L value of the colorimetric measurement test piece was measured using a color difference meter. The lower the L value, the darker the black color, which means better pigment colorability.
- Examples 1 to 16 and Comparative Examples 1 to 10 were expressed by the rubber morphologies of Equations 1 and 2, and the refractive index difference (the refractive index of the seed and the shell was 0.03 or less compared to the matrix resin, and the refractive index of the core was 0.08 or more relative to the resin) and the like.
- Example 1 19 1.6 95 27.0 Example 2 16 1.4 98 26.5 Example 3 23 1.9 92 27.2 Example 4 25 2.0 91 27.5 Example 5 18 1.5 95 26.8 Example 6 29 1.5 95 26.9 Example 7 18 1.7 99 27.3 Example 8 24 1.8 93 27,4 Example 9 17 1.4 98 26.3 Example 10 18 1.5 96 26.5 Example 11 18 1.5 98 26.7 Example 12 19 1.4 95 26.9 Example 13 19 1.4 96 26.8 Example 14 18 1.6 97 26.7 Example 15 21 1.6 94 27.3 Example 16 18 1.2 96 26.5
- Examples 1 to 16 are all excellent compared with Comparative Examples 1 to 10, while maintaining the impact strength equal or more, excellent in colorability and gloss, excellent in appearance characteristics, excellent weather resistance, and overall physical properties. The balance was excellent.
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Abstract
Description
구분 | 비교예 1-5 | 비교예 6-8 | 비교예 9-10 |
시드 굴절율 | 부적절 | ||
코어 굴절율 | 부적절 | ||
코어 두께/사이즈 | 부적절 |
구분 | 충격강도 | 내후성 | 광택 | 착색성 |
실시예 1 | 19 | 1.6 | 95 | 27.0 |
실시예 2 | 16 | 1.4 | 98 | 26.5 |
실시예 3 | 23 | 1.9 | 92 | 27.2 |
실시예 4 | 25 | 2.0 | 91 | 27.5 |
실시예 5 | 18 | 1.5 | 95 | 26.8 |
실시예 6 | 29 | 1.5 | 95 | 26.9 |
실시예 7 | 18 | 1.7 | 99 | 27.3 |
실시예 8 | 24 | 1.8 | 93 | 27,4 |
실시예 9 | 17 | 1.4 | 98 | 26.3 |
실시예 10 | 18 | 1.5 | 96 | 26.5 |
실시예 11 | 18 | 1.5 | 98 | 26.7 |
실시예 12 | 19 | 1.4 | 95 | 26.9 |
실시예 13 | 19 | 1.4 | 96 | 26.8 |
실시예 14 | 18 | 1.6 | 97 | 26.7 |
실시예 15 | 21 | 1.6 | 94 | 27.3 |
실시예 16 | 18 | 1.2 | 96 | 26.5 |
구분 | 충격강도 | 내후성 | 광택 | 착색성 |
비교예 1 | 22 | 2.0 | 85 | 29.0 |
비교예 2 | 6 | 1.5 | 95 | 26.5 |
비교예 3 | 25 | 1.7 | 81 | 29.3 |
비교예 4 | 25 | 1.6 | 88 | 29.8 |
비교예 5 | 21 | 1.5 | 75 | 30.6 |
비교예 6 | 16 | 1.4 | 95 | 29.2 |
비교예 7 | 20 | 1.5 | 91 | 29.5 |
비교예 8 | 19 | 1.5 | 93 | 29.4 |
비교예 9 | 7 | 1.6 | 95 | 26.5 |
비교예 10 | 25 | 8.6 | 98 | 26.5 |
Claims (15)
- 시드, 코어 및 쉘로 구성된 ASA계 그라프트 공중합체; 및 매트릭스 중합체;를 포함하여 이루어지되,상기 시드와 쉘의 굴절율은 상기 매트릭스 중합체의 굴절율(μD 25)과의 차이가 각각 0.035 미만이고,상기 코어의 굴절율은 상기 매트릭스 중합체의 굴절율(μD 25)과의 차이가 0.056 초과이며,상기 ASA 그라프트 공중합체는 하기 수학식 1 및 2를 동시에 만족시키는 것을 특징으로 하는 ASA계 그라프트 공중합체 조성물.[수학식 1]140<2*r2<380[수학식 2]r2-r1<80(상기 수학식 1, 2에서, r1은 상기 그라프트 공중합체의 중심으로부터 시드까지의 두께(nm)이고, r2는 상기 그라프트 공중합체의 중심으로부터 코어까지의 두께(nm)이다.)
- 제1항에 있어서,상기 ASA계 그라프트 공중합체는 겔 함량이 92% 미만인 것을 특징으로 하는 ASA계 그라프트 공중합체 조성물.
- 제1항에 있어서,상기 ASA 그라프트계 공중합체는 그라프트율이 20% 초과인 것을 특징으로 하는 ASA계 그라프트 공중합체 조성물.
- 제1항에 있어서,상기 ASA계 그라프트 공중합체는 방향족 비닐 화합물, 비닐시안 화합물, 및 알킬 (메타)아크릴레이트 화합물 중 1종 이상의 화합물을 포함하여 이루어지는 시드; 상기 시드를 감싸며, 알킬 아크릴레이트를 포함하여 이루어지는 고무 코어; 및 상기 코어를 감싸며, 방향족 비닐 화합물, 비닐시안 화합물 및 알킬 (메타)아크릴레이트 화합물 중 1종 이상의 화합물을 포함하여 이루어지는 쉘;을 포함하는 것을 특징으로 하는 ASA계 그라프트 공중합체 조성물.
- 제1항에 있어서,상기 시드 대 코어 대 쉘의 중량비가 5~40: 20~60: 20~60 범위 내인 것을 특징으로 하는 ASA계 그라프트 공중합체 조성물.
- 제4항에 있어서,상기 알킬 아크릴레이트는 메틸아크릴레이트, 에틸아크릴레이트, 프로필아크릴레이트, 부틸아크릴레이트, 헥실아크릴레이트, 옥틸아크릴레이트 및 2-에틸헥실아크릴레이트로 이루어진 군으로부터 선택된 하나 이상인 것을 특징으로 하는 ASA계 그라프트 공중합체 조성물.
- 제4항에 있어서,상기 방향족 비닐 화합물은 스티렌, α-스티렌, p-스티렌 및 비닐 톨루엔의 스티렌 단량체 유도체로 이루어지는 군으로부터 선택된 1종 이상인 것을 특징으로 하는 ASA계 그라프트 공중합체 조성물.
- 제4항에 있어서,상기 비닐시안 화합물은 아크릴로니트릴, 메타크릴로니트릴, 또는 이들의 혼합인 것을 특징으로 하는 ASA계 그라프트 공중합체 조성물.
- 제4항에 있어서,상기 알킬 (메타)아크릴레이트 화합물은 메틸아크릴레이트, 에틸아크릴레이트, 프로필아크릴레이트, 부틸아크릴레이트, 2-에틸헥실아크릴레이트, 메틸메타크릴레이트, 에틸메타크릴레이트 프로필메타크릴레이트, 2-에틸헥실 메타크릴레이트, 메틸에타크릴레이트 및 에틸에타크릴레이트로 이루어지는 군으로부터 선택된 1종 이상인 것을 특징으로 하는 ASA계 그라프트 공중합체 조성물.
- 제1항에 있어서,상기 시드, 코어 또는 이들 모두가, 디비닐벤젠, 1,3-부탄디올 디아크릴레이트, 1,3-부탄디올 디메타크릴레이트, 1,4-부탄디올 디아크릴레이트, 1,4-부탄디올 디메타크릴레이트, 아릴 아크릴레이트, 아릴 메타크릴레이트, 트리메틸올프로판 트리아크릴레이트, 테트라에틸렌글리콜 디아크릴레이트, 에틸렌글리콜 디메타크릴레이트, 디에틸렌글리콜 디메타크릴레이트, 트리에틸렌글리콜 디메타크릴레이트, 네오펜틸 글리콜 디메타크릴레이트, 트리알릴 이소시아누레이트, 트리아릴아민, 디알릴아민 및 하기 화학식 1로 표시되는 화합물로 이루어진 군으로부터 선택된 1종 이상을 가교제로 포함하는 것을 특징으로 하는 ASA계 그라프트 공중합체 조성물.[화학식 1](상기 식에서, A는 독립적으로 비닐기를 가진 치환기 혹은 (메트)아크릴레이트기이고, A'는 수소기, 비닐기를 가진 치환기, 탄소수 1 내지 30의 알킬기 혹은 탄소수 5 내지 24의 아릴알킬기, 혹은 탄소수 5 내지 24의 아릴아민기, 혹은 탄소수 6 내지 30의 아릴기이고, R은 독립적으로 에틸기 혹은 프로필기이고, n은 0 내지 15의 정수이다.)
- 제10항에 있어서,상기 가교제는 ASA계 그라프트 공중합체 제조시 사용되는 단량체 총 100 중량부를 기준으로 0.01 내지 5 중량부 범위내로 사용하는 것을 특징으로 하는 ASA계 그라프트 공중합체 조성물.
- 제1항에 있어서,상기 매트릭스 중합체는 방향족 비닐 화합물, 비닐시안 화합물 및 알킬 (메타)아크릴레이트 화합물 중 1종 이상의 화합물을 포함하는 경질 매트릭스 중합체 중 선택된 1종 이상인 것을 특징으로 하는 ASA계 그라프트 공중합체 조성물.
- 제1항에 있어서,상기 ASA계 그라프트 공중합체와 매트릭스 중합체는 10:90 내지 90:10의 중량비로 포함되는 것을 특징으로 하는 ASA계 그라프트 공중합체 조성물.
- 제1항에 있어서,상기 ASA계 그라프트 공중합체 조성물은 난연제, 활제, 항균제, 이형제, 핵제, 가소제, 열안정제, 산화방지제, 광안정제, 상용화제, 안료, 염료 및 무기물 첨가제로 이루어진 군으로부터 선택된 하나 이상의 첨가제를 ASA계 그라프트 공중합체 조성물 총 100 중량부를 기준으로 0.1 내지 10 중량부 범위 내로 포함하는 것을 특징으로 하는 ASA계 그라프트 공중합체 조성물.
- 제1항 내지 제14항 중 어느 한 항의 ASA계 그라프트 공중합체 조성물로부터 제조됨을 특징으로 하는 성형품.
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US14/118,678 US9353255B2 (en) | 2012-08-27 | 2013-07-16 | Acrylonitrile-acrylate-styrene graft copolymer and thermoplastic resin composition comprising thereof |
JP2014533228A JP5948716B2 (ja) | 2012-08-27 | 2013-07-16 | アクリロニトリル−アクリレート−スチレングラフト共重合体、及びそれを含む熱可塑性樹脂組成物 |
EP13788870.7A EP2889317B1 (en) | 2012-08-27 | 2013-07-16 | Acrylonitrile-acrylate-styrene graft copolymer and thermoplastic resin composition including same |
CN201380002159.0A CN103764700B (zh) | 2012-08-27 | 2013-07-16 | 丙烯腈-丙烯酸酯-苯乙烯接枝共聚物和包含该共聚物的热塑性树脂组合物 |
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CN109627621B (zh) * | 2018-10-31 | 2021-07-20 | 浙江科普特新材料有限公司 | 一种高光、高表面硬度asa材料及其制备方法 |
CN111087554A (zh) * | 2019-12-24 | 2020-05-01 | 广州熵能创新材料股份有限公司 | 一种高抗冲丙烯酸酯-苯乙烯-丙烯腈接枝聚合物及其制备方法和应用 |
Also Published As
Publication number | Publication date |
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EP2889317B1 (en) | 2016-12-07 |
US9353255B2 (en) | 2016-05-31 |
CN103764700A (zh) | 2014-04-30 |
CN103764700B (zh) | 2016-09-21 |
US20140235749A1 (en) | 2014-08-21 |
JP2014527570A (ja) | 2014-10-16 |
KR20140027872A (ko) | 2014-03-07 |
KR101425754B1 (ko) | 2014-08-05 |
EP2889317A1 (en) | 2015-07-01 |
EP2889317A4 (en) | 2016-03-30 |
JP5948716B2 (ja) | 2016-07-06 |
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