Description

IMPACT MODIFIER, METHOD FOR PREPARING THE SAME

AND SCRATCH RESISTANT METHACRYLATE RESIN

COMPOSITION USING THE SAME

Technical Field

[1] The present invention relates to an impact modifier capable of improving impact resistance while maintaining transparency and scratch resistance, a method for preparing the same, and a scratch resistant methacrylate-based resin composition using the same. More particularly, the present invention relates to a scratch resistant resin impact modifier capable of improving impact resistance while maintaining transparency and scratch resistance, a method for preparing the same, and a scratch resistant methacrylate-based resin composition using the same.

[2]

Background Art

[3] In general, methacrylate-based resins have sufficient stiffness, high transmittance and excellent scratch resistance resulting from superior stiffness. Due to such characteristics, methacrylate-based resins are used in various fields. Injection molded articles of methacrylate-based resins are used as rear lamp assemblies for automobiles, instrument panel covers for automobiles, eyeglass lenses, or the like, and extruded articles of methacrylate-based resins are used as signboards and various sheet products.

[4] However, such methacrylate-based resins have a problem in that mechanical properties, particularly, impact resistance, are deteriorated. It is hard to use methacrylate-based resins as resins for housings requiring impact resistance due to the deterioration of the mechanical properties, particularly, impact resistance.

[5] Furthermore, although methacrylate-based resins have excellent surface scratch resistance resulting from superior stiffness, methacrylate-based resins have a problem in that rubbing resistance is deteriorated since fine scratches are generated on the surface of methacrylate-based resins by repeated rubbing with soft cotton or a kind of towel due to the superior stiffness of methacrylate-based resins.

[6] Although surface characteristics and impact resistance of methacrylate-based resins can be partially improved by introducing a soft impact modifier into methacrylate- based resins in order to improve impact resistance and rubbing resistance, the transparency of methacrylate-based resins is rapidly lowered relatively when a soft impact modifier is introduced into methacrylate-based resins.

[7] Some impact modifiers that partially prevent transparency from being lowered and can improve impact resistance have been developed, but the impact modifiers have a

low improvement degree of impact resistance. [8] Therefore, the present inventors have developed an impact modifier having excellent surface characteristics while improving transparency and impact resistance by adding an antioxidant when an impact modifier is polymerized, and a method for preparing the impact modifier. [9]

Disclosure of Invention

Technical Problem [10] An object of the present invention is to provide an impact modifier capable of improving impact strength. [11] Another object of the present invention is to provide an impact modifier that can improve rubbing resistance and scratch resistance. [12] A further object of the present invention is to provide an impact modifier that can improve impact strength without deteriorating transparency. [13] A still further object of the present invention is to provide an impact modifier capable of improving the balance of physical properties such as flowability, yellow index, impact strength, scratch resistance and the like. [14] A still further object of the present invention is to provide a method for preparing an impact modifier with excellent reaction stability. [15] A still further object of the present invention is to provide a method for preparing an impact modifier which does not deteriorate transmittance and mechanical properties. [16] A still further object of the present invention is to provide a methacrylate -based resin composition having excellent impact resistance, scratch resistance, transparency and appearance by employing the aforementioned impact modifier. [17] Other objects and advantages of this invention will be apparent from the ensuing disclosure and appended claims. [18]

Technical Solution [19] One aspect of the invention provides an impact modifier formed by graft polymerizing about 45 to 70 % by weight of a rubber polymer with about 30 to 55 % by weight of a methacrylate-based monomer, wherein the rubber polymer is prepared by polymerizing about 0.1 to 1 part by weight of an antioxidant with about 100 parts by weight of a monomer mixture comprising about 30 to 45 % by weight of a diene - based monomer and about 55 to 70 % by weight of alkyl acrylate. [20] In exemplary embodiments of the invention, the methacrylate-based monomer is alkyl methacrylate having 1 to 10 carbon atoms. [21] In embodiments, the alkyl acrylate is alkyl acrylate having 1 to 10 carbon atoms.

[22] The antioxidant may be octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, triethylene glycol-bis-3(3-tert-butyl-4-hydroxy-5-methylphenyl)propionat e, 2,6-di-tert-butyl-4-methylphenol, 2,2 ^/ -methylene-bis-(4-methyl-6-tert-butylphenol), tri(2,4-di-tert-butylphenyl)phosphate, n- octadecyl-3(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, l,3,5-tri(3,5-di-tert-butyl-4-hydroxyphenyl)isocyanate, 3-(3,5-di-tert-butyl-4-hydroxyphenyl), distearyl-thio-dipropionate, laurylthio propionate methane, di-phenyl-isooctyl phosphite, or mixtures thereof.

[23] Another aspect of the invention provides a method for preparing the foregoing impact modifier. The method comprises the steps of: polymerizing a monomer mixture comprising a diene-based monomer and alkyl acrylate in the presence of an antioxidant to prepare a rubber polymer with a particle diameter of about 150 to 250 nm; and adding a methacrylate-based monomer into the rubber polymer to graft polymerize the methacrylate-based monomer with the rubber polymer.

[24] In exemplary embodiments of the invention, the monomer mixture comprises about

30 to 45 % by weight of the diene-based monomer and about 55 to 70 % by weight of the alkyl acrylate.

[25] In one embodiment, the alkyl acrylate is alkyl acrylate having 1 to 10 carbon atoms.

[26] In one embodiment, the methacrylate-based monomer is alkyl methacrylate having

1 to 10 carbon atoms.

[27] In exemplary embodiments of the invention, the monomer mixture may be polymerized using a cross-linking agent and a molecular weight controlling agent.

[28] The cross-linking agent may be triallyl isocyanurate, allyl methacrylate, or a mixture thereof. The cross-linking agent may be used in an amount of about 0.5 to 1 part by weight, per about 100 parts by weight of the monomer mixture.

[29] The antioxidant may be octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate or triethylene glycol-bis-3(3-tert-butyl-4-hydroxy-5-methylphenyl)propionat e, 2,6-di-tert-butyl-4-methylphenol, 2,2 ^/ -methylene-bis-(4-methyl-6-tert-butylphenol), tri(2,4-di-tert-butylphenyl)phosphate, n- octadecyl-3(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, l,3,5-tri(3,5-di-tert-butyl-4-hydroxyphenyl)isocyanate, 3-(3,5-di-tert-butyl-4-hydroxyphenyl), distearyl-thio-dipropionate, laurylthio propionate methane, di-phenyl-isooctyl phosphite, or mixtures thereof. The antioxidant may be used in an amount of about 0.1 to 1 part by weight of the antioxidant, per about 100 parts by weight of the monomer mixture.

[30] In embodiments, the methacrylate-based monomer may be introduced when a conversion ratio of the rubber polymer is about 70 to 98 %.

[31] Another aspect of the invention provides a methacrylate-based resin composition

comprising the foregoing impact modifier. The methacrylate-based resin composition comprises about 55 to 95 % by weight of a methacrylate-based resin and about 5 to 45 % by weight of an impact modifier.

[32] Another aspect of the invention provides a molded article using the resin composition.

[33] The molded article may be prepared by molding the methacrylate-based resin composition of the present invention, wherein the molded article has an Izod notched impact strength of about 4.5 kgf-D/D or more at a thickness of 1/4" according to ASTM D256, a yellow index of about 1.7 or less according to ASTM D 1925, a pencil hardness of IH or more at a load of 500 g and a temperature of 23 ⁰ C according to JIS K5401, a total light transmittance of about 92 % or more and a haze of about 0.9 % or less respectively measured by a color computer manufactured by Suga Instrument Corporation.

[34]

Best Mode for Carrying Out the Invention

[35] An impact modifier of the present invention is formed by graft polymerizing about

45 to 70 % by weight of a rubber polymer with about 30 to 55 % by weight of a methacrylate-based monomer, wherein the rubber polymer is prepared by polymerizing about 0.1 to 1 part by weight of an antioxidant with about 100 parts by weight of a monomer mixture comprising about 30 to 45 % by weight of a diene-based monomer and about 55 to 70 % by weight of alkyl acrylate.

[36] The monomer used in the preparation of the rubber polymer may have a low glass transition temperature such that the monomer can exhibit rubber characteristics, and a composition of the monomer may be controlled to maintain the same refractive index as that of a methacrylate-based resin. For instance, it is preferable to control a refractive index to be within a range of a refractive index of a poly(methyl methacrylate) resin of about 1.49 ±0.005.

[37] A monomer having a low glass transition temperature can be used as the diene- based monomer, and preferably a monomer having a glass transition temperature of about 70 ⁰ C or less may be used. Examples of the diene-based monomer may include 1,3-butadiene, 2-methyl-l,3-butadiene, 2,3-methyl-l,3-butadiene, 1,3-pentadiene, 1,3-hexadiene and mixtures thereof. Preferably butadiene may be used as the diene- based monomer.

[38] The alkyl acrylate may be an alkyl acrylate having 1 to 10 carbon atoms. Specific examples of the alkyl acrylate may include octyl acrylate, methyl acrylate, ethyl acrylate, butyl acrylate, or the like. Preferably, butyl acrylate that is inexpensive is used as the alkyl acrylate.

[39] An alkyl methacrylate having 1 to 10 carbon atoms may be used as the methacrylate-based monomer. Examples of the methacrylate-based monomer may include methyl methacrylate, ethyl methyl methacrylate, propyl methyl methacrylate, butyl methyl methacrylate, hexyl methyl methacrylate, 2-ethylhexyl methyl methacrylate, octyl methyl methacrylate, or mixtures thereof. Preferably, the methyl methacrylate is used as the methacrylate-based monomer.

[40] In addition, an antioxidant may be used during the preparation of the rubber polymer in the present invention in order to prevent oxidation of a copolymer rubber and lower yellow index of the copolymer rubber. It is preferable to use secondary antioxidants such as a thiol-based antioxidant and a phosphorous-based antioxidant. Examples of the antioxidant may include octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, Methylene glycol- bis-3(3-tert-butyl-4-hydroxy-5-methylphenyl)propionate,

2,6-di-tert-butyl-4-methylphenol, 2,2 ^/ -methylene-bis-(4-methyl-6-tert-butylphenol), tri(2,4-di-tert-butylphenyl)phosphate, n- octadecyl-3(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, l,3,5-tri(3,5-di-tert-butyl-4-hydroxyphenyl)isocyanate, 3-(3,5-di-tert-butyl-4-hydroxyphenyl), distearyl-thio-dipropionate, laurylthio propionate methane, di-phenyl-isooctyl phosphite, or mixtures thereof. These antioxidants can be used alone or in combination with one another.

[41] It is preferable that the antioxidant is used in an amount of about 0.1 to 1 part by weight, per about 100 parts by weight of the monomer mixture. In a case where the antioxidant of the present invention is used in the aforementioned range, an anti- oxidation effect resulting from butadiene can be obtained, and polymerization can proceed smoothly without deterioration in the polymerization reaction.

[42] The rubber polymer may be prepared by polymerizing about 30 to 45 % by weight of a diene-based monomer and about 55 to 70 % by weight of an alkyl acrylate in the presence of an antioxidant. In case of the polymerization in the aforementioned ratio, a refractive index difference between the rubber polymer and a methacrylate-based resin can be minimized, and a final resin composition can maintain superior transparency. More preferably, the rubber polymer is prepared by polymerizing about 35 to 43 % by weight of the diene-based monomer and about 57 to 65 % by weight of the alkyl acrylate in the presence of the antioxidant.

[43] The rubber polymer of the present invention may have an average particle diameter range of about 150 to 250 nm, preferably about 170 to 230 nm, more preferably about 175 to 220 nm. In a case where the rubber polymer has such a range, the rubber polymer can obtain a preferable effect with respect to impact resistance and transparency.

[44] An impact modifier of the present invention can be prepared by graft polymerizing a methacrylate-based monomer with the rubber polymer.

[45] About 45 to 70 % by weight of the rubber polymer is mixed with about 30 to 55 % by weight of the methacrylate-based monomer in the graft polymerization. In a case where the aforementioned mixing ratio is used, the obtained impact modifier can be excellent in production efficiency, graft polymerization efficiency, and impact resistance. Furthermore, since a uniform graft polymerization can be performed, the impact modifier can be uniformly dispersed after performing an extrusion or an injection molding process. Preferably, about 47 to 65 % by weight of the rubber polymer is mixed with about 35 to 53 % by weight of the methacrylate-based monomer in the graft polymerization. More preferably, about 49 to 63 % by weight of the rubber polymer is mixed with about 37 to 51 % by weight of the methacrylate-based monomer.

[46] The impact modifier according to the present invention can be prepared by the following method.

[47] First, a rubber polymer for improving impact resistance is prepared, and then an impact modifier can be prepared by performing a graft polymerization using a methyl methacrylate monomer to provide compatibility of the rubber polymer with a methacrylate-based resin.

[48] In one embodiment of the present invention, the impact modifier may be prepared by polymerizing a monomer mixture comprising a diene-based monomer and an alkyl acrylate in the presence of an antioxidant to prepare a rubber polymer with a particle diameter of about 150 to 250 nm, and adding a methacrylate-based monomer into the rubber polymer to graft-polymerize them.

[49] As mentioned above, the diene-based monomer and the alkyl acrylate with low glass transition temperatures are selected such that the diene-based monomer and the alkyl acrylate can exhibit rubber characteristics, and specific examples of the diene- based monomer and the alkyl acrylate are the same as the aforementioned examples.

[50] The monomer mixture comprises about 30 to 45 % by weight of the diene-based monomer and about 55 to 70 % by weight of the alkyl acrylate such that a refractive index is maintained within a range of a refractive index of a poly(methyl methacrylate) resin of about 1.49 +0.005.

[51] The monomer mixture can be polymerized in the presence of additives such as a cross-linking agent, a molecular weight controlling agent, an emulsifier, an electrolyte, and the like.

[52] In exemplary embodiments of the invention, the rubber polymer can be prepared in an emulsion polymerization by adding a cross-linking agent, a molecular weight controlling agent and an emulsifier to a monomer mixture comprising a diene-based

monomer and an alkyl acrylate in the presence of an antioxidant.

[53] In another embodiment of the present invention, the rubber polymer can be prepared in an emulsion polymerization by adding a cross-linking agent, a molecular weight controlling agent, an emulsifier and an electrolyte to a monomer mixture comprising a diene-based monomer and an alkyl acrylate in the presence of an antioxidant.

[54] In another embodiment of the present invention, the rubber polymer can be prepared by adding a cross-linking agent, a molecular weight controlling agent, an emulsifier and an electrolyte to a monomer mixture comprising a diene-based monomer and an alkyl acrylate in the presence of an antioxidant, heating the reaction temperature to about 50~80 ⁰ C, preferably about 60~75 ⁰ C, and introducing an initiator thereinto to initiate an emulsion polymerization.

[55] Triallyl isocyanate (TAIC), allyl methacrylate (AMA) or a mixture thereof may be used as the cross-linking agent. It is preferable to use about 0.5 to 1 part by weight of the cross-linking agent with respect to about 100 parts by weight of the monomer mixture. When the cross-linking agent is used in such a range, an optimal effect can be obtained with regard to transmittance and impact resistance.

[56] The molecular weight controlling agent may include alkyl mercaptanes in the form of CH 3 (CH 2 ) n SH such as n-butyl mercaptane, n-octyl mercaptane, n-dodectl mercaptane, tertiary dodecyl mercaptane, isopropyl mercaptane and n-amyl mercaptane, and aromatic compounds such as alpha methyl styrene dimers, alpha ethyl styrene dimers and halogen compounds including carbon tetra chloride. The n-octyl mercaptane is preferably used as the molecular weight controlling agent.

[57] It is preferable in the present invention that about 0.2 to 1 part by weight of the molecular weight controlling agent with respect to about 100 parts by weight of the monomer mixture be used. When such a range is used, excellent mechanical properties can be obtained.

[58] Fatty acid-based emulsifiers such as derivatives in which lauric acid, stearic acid, oleic acid, and the like are substituted with sodium or potassium are preferable as the emulsifiers. It is preferable that about 1 to 3 parts by weight of the emulsifier with respect to about 100 parts by weight of the monomer mixture be used. When the emulsifier is used in such a range, emulsion stability is maintained to prevent the problem of deteriorated impact resistance due to a large particle diameter of 250 nm or greater or a small particle diameter and to prevent the problem of deteriorated transparency due to residual emulsifier.

[59] An electrolyte may be used to improve emulsion stability in the preparation of the rubber polymer. Potassium carbamate is preferably used as the electrolyte, but the electrolyte is not limited thereto. It is preferable to use about 1 to 3 parts by weight of

the electrolyte with respect to about 100 parts by weight of the monomer mixture. When such a range is used, this is preferable with regard to polymerization stability and it is possible to prevent the problem of emulsion stability deterioration caused by macronization of particle diameter and high viscosity of particles.

[60] A water-soluble initiator is used as the initiator used in a rubber polymer of the present invention, and particularly a persulfate-based initiator is preferable. The water- soluble initiator includes sodium persulfate, ammonium persulfate, potassium persulfate, and the like. In the present invention, about 0.3 to 1 part by weight of the initiator with respect to about 100 parts by weight of the monomer mixture is preferably used. When such a range is used, it is possible to obtain excellent reactivity and prevent the deterioration of physical properties due to a reduction of molecular weight without being affected by a polymerization inhibitor and impurities remaining in the monomer.

[61] In a conventional method for preparing a rubber polymer, a core/shell rubber can be prepared in such a manner that a core is formed using a monomer with a high glass transition temperature, the core is covered with a rubber with a low glass transition temperature, and then a hard core is formed in the rubber. However, a rubber is prepared in the present invention by a polymerization method in which a relatively hard rubber is formed by increasing the degree of cross-linking of a rubber formed in the early reaction stage using a mixture of a cross-linking agent having a relatively fast reactivity and a molecular weight controlling agent and a soft rubber is then formed in the second half of the polymerization process.

[62] The rubber is graft polymerized by a methacrylate-based monomer in order to exhibit compatibility with methacrylate resins.

[63] The graft polymerization is performed by adding a methacrylate-based monomer into the rubber at a time point when a predetermined polymerization ratio has passed during the preparation of a rubber polymer.

[64] It is desirable to inject the methacrylate monomer at a graft polymerization time point at which a copolymer rubber has a conversion rate of about 70 % to 98 %, preferably about 90 % to 96 %. If the methacrylate monomer is introduced at a graft polymerization time point at which the copolymer rubber has a conversion rate of less than about 70 %, impact resistance of a prepared impact modifier can be deteriorated. If the methacrylate monomer is introduced at a graft polymerization time point at which the copolymer rubber has a conversion rate of greater than about 98 %, stability of the impact modifier can be deteriorated since a free methacrylate polymer that is not graft polymerized is excessively formed due to a deficient graft polymerization site.

[65] In order to obtain transparency, it is preferable to inject the methacrylate monomer when the rubber has an average particle diameter of about 150 to 250 nm.

[66] In the present invention, the predetermined amount of a molecular adjusting agent may be used to adjust the molecular weight of a polymer produced during the graft polymerization.

[67] In a preferred embodiment of the present invention, a mixture of the molecular weight controlling agent and the methacrylate monomer is introduced at a time point at which the rubber has a conversion ratio of about 70 % to 98 %.

[68] The molecular weight controlling agent used during the graft polymerization includes the aforementioned molecular weight controlling agent used in the preparation of the rubber. In one embodiment of the present invention, n-octyl mercaptane is used. In the present invention, about 0.2 to 1 part by weight of the molecular weight controlling agent with respect to about 100 parts by weight of a mixture of a rubber polymer and a methacrylate monomer is preferably used during the graft polymerization. When such a range is used, excellent mechanical properties can be obtained.

[69] The prepared graft polymer is post-treated in an ordinary manner and can be used as an impact modifier. For instance, a final impact modifier can be prepared in the form of powder, particulate, particle, granule, or the like, but the form is not limited thereto.

[70] In one embodiment of the present invention, the prepared graft polymer is formed into a powder impact modifier through a post-treatment process and a dehydrating and drying process using a coagulant.

[71] When an impact modifier according to the present invention is applied to resins, it is possible to improve transparency, scratch resistance and surface characteristics as well as impact resistance of the resins.

[72] In particular, when the impact modifier is applied to methacrylate-based resins, it is possible to obtain an effect of improving transparency and scratch resistance.

[73] The present invention provides a methacrylate-based resin composition to which the impact modifier is applied. The methacrylate-based resin composition comprises about 55 to 95 % by weight of a methacrylate-based resin and about 5 to 45 % by weight of an impact modifier. The methacrylate-based resin is preferably a poly(methyl methacrylate). The methacrylate-based resin composition may be prepared by blending the impact modifier with a methacrylate-based resin.

[74] The present invention provides a molded article using the resin composition.

[75] The molded article is manufactured by molding a methacrylate-based resin composition of the present invention, wherein the molded article has an Izod notched impact strength of about 4.5 kgf-D/D or more at a thickness of 1/4" according to ASTM D256, a yellow index of about 1.7 or less according to ASTM D 1925, a pencil hardness of IH or more at a load of 500 g and a temperature of 23 ⁰ C according to JIS K5401, a total light transmittance of about 92 % or more and a haze of about 0.9 % or

less respectively measured by a color computer manufactured by Suga Instrument Corporation.

[76] In one embodiment of the present invention, the molded article has an Izod notched impact strength of about 4.5 to about 9.0 kgf-D/D at a thickness of 1/4" according to ASTM D256, a yellow index of about 1.0 to about 1.7 according to ASTM D 1925, a pencil hardness of IH to 4H at a load of 500 g and a temperature of 23 ⁰ C according to JIS K5401, a total light transmittance of about 92 % to about 98 % and a haze of about 0.5 to about 0.9 % respectively measured by a color computer manufactured by Suga Instrument Corporation.

[77] The methacrylate-based resin composition of the present invention may further comprise general additives such as flame retardants, lubricants, releasing agents, nucleating agents, antistatic agents, stabilizers and a reinforcing agent according to respective uses in addition to the foregoing components. One of the additives may be used alone or a mixture of at least two thereof may also be used.

[78] The methacrylate-based resin composition of the present invention has excellent impact resistance, scratch resistance, transparency and external appearance. Therefore, the methacrylate-based resin composition of the present invention can replace conventional methyl methacrylate resins and can be used in housings for various electrical and electronic appliances as well. For instance, the methacrylate-based resin composition of the present invention can be used for housings of various electrical and electronic appliances, such as television sets, computers, printers, washing machines, cassette players and audios, as well as rear lamp assemblies, instrument panel covers, eyeglass lenses, signboards and various sheet products.

[79] The invention may be better understood by reference to the following examples which are intended for the purpose of illustration and are not to be construed as in any way limiting the scope of the present invention, which is defined in the claims appended hereto.

[80]

Mode for the Invention

[81] EXAMPLES

[82]

[83] Example 1

[84] To a high pressure reactor were added 36.3 parts by weight of a butyl acrylate monomer, 132 parts by weight of process water, 0.6 part by weight of a cross-linking agent (TAIC), 0.3 part by weight of a molecular weight controlling agent (n-octyl mercaptane), 2.0 parts by weight of an electrolyte (potassium carbamate), 2.0 parts by weight of an emulsifier (potassium stearate) and 0.6 part by weight of an antioxidant

(octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate), and the reactor was sealed and clamped. After assessing a leak part of the reactor by pressurizing nitrogen into the reactor in order to conduct an air-tightness assessment of the reactor, 23.7 parts by weight of a butadiene monomer was introduced into the reactor. After increasing a temperature of the reactor to 70 ⁰ C, 0.8 part by weight of an initiator (potassium persulfate) was added into the reactor to initiate the reaction. The temperature of the reactor was maintained at 70 ⁰ C by using a heat medium and cooling water in a reactor jacket. The polymerization ratio and the particle diameter were measured at a time point when 4 hours were has passed after the initiator was added into the reactor, and the measured polymerization ratio and particle diameter were 94 % and 200 nm respectively. While increasing a temperature of the reactor to 85 ⁰ C for one hour, 40 parts by weight of a methyl methacrylate monomer is mixed with 0.5 part by weight of a molecular weight controlling agent (n-octyl mercaptane), and then, the mixture was continuously introduced into the reactor for 30 minutes for a graft polymerization. The reactor was cooled to finish the polymerization after maintaining the temperature of the reactor to 85 ⁰ C for about 3 hours after the methyl methacrylate monomer was introduced into the reactor. A composition for the prepared impact modifier contained a rubber comprising 60.5 % by weight of a butyl acrylate monomer and 39.5 % by weight of a butadiene monomer, and comprised 60 % by weight of a rubber polymer and 40 % by weight of a methyl methacrylate monomer.

[85] After analyzing the prepared sample in a latex state, the mixture was agglomerated by slowly adding 100 parts by weight of the analyzed sample into 140 parts by weight of a 1% sulfuric acid solution that was rotated at a rotational speed of 250 rpm and maintained at 67 ⁰ C. Hard agglomerated particles were formed by increasing a temperature of the agglomerated mixture to 90 ⁰ C, the hard agglomerated particles were dehydrated by a centrifuge, and the dehydrated agglomerated particles were dried to a water content of not more than 0.5 % by a fluidized-bed dryer. To 20 parts by weight of the dried sample, 80 parts by weight of PMMA with a weight average molecular weight of 97,000 was added and extruded to prepare a test specimen at an extrusion temperature of 230 ⁰ C using an extrusion and injection molding machine. The physical properties of the test specimens were measured, and the results are shown in Table 1.

[86]

[87] Example 2

[88] Example 2 is prepared in the same manner as in Example 1 except that the polymerization ratio, the particle diameter and the methyl methacrylate injecting time were respectively changed to 96 %, 198 nm and 80 minutes by extending a rubber polymer polymerizing time by 1 more hour, i.e., by polymerizing the rubber polymer for 5

hours.

[89]

[90] Example 3

[91] Example 3 is prepared in the same manner as in Example 1 except that the contents of the rubber polymer and the methyl methacrylate monomer were changed to 55 % by weight and 45 % by weight, respectively, and the graft polymerization was performed at a rubber polymer particle diameter of 178 nm.

[92]

[93] Comparative Example 1

[94] Comparative Example 1 is prepared in the same manner as in Example 1 except that the contents of the butadiene monomer and the butyl acrylate monomer were changed to 30 parts by weight and 30 parts by weight, respectively.

[95]

[96] Comparative Example 2

[97] Comparative Example 2 is prepared in the same manner as in Example 1 except that the contents of the rubber polymer and the methyl methacrylate monomer were changed to 80 % by weight and 20 % by weight, respectively, and the graft polymerization was performed at a rubber polymer particle diameter of 251 nm.

[98]

[99] Comparative Example 3

[100] Comparative Example 3 is prepared in the same manner as in Example 1 except that the contents of the rubber polymer and the methyl methacrylate monomer were changed to 50 % by weight and 50 % by weight, respectively, and the graft polymerization was performed at a rubber polymer particle diameter of 142 nm.

[101]

[102] Comparative Example 4

[103] Comparative Example 4 is prepared in the same manner as in Example 1 except that the content of the emulsifier was changed to 0.8 part by weight during the preparation of the rubber polymer, and the graft polymerization was performed at a rubber polymer particle diameter of 332 nm.

[104]

[105] Comparative Example 5

[106] Comparative Example 5 is prepared in the same manner as in Example 1 except that the content of the cross-linking agent was changed to 2.0 parts by weight.

[107]

[108] Comparative Example 6

[109] Comparative Example 6 is prepared in the same manner as in Example 1 except that the antioxidant was not used.

[HO]

[111] Comparative Example 7

[112] PMMA with a weight average molecular weight of 97,000 solely was extruded to prepare a test specimen at an extrusion temperature of 230 ⁰ C using an extrusion and injection molding machine. The physical properties of the test specimens were measured, and the results are shown in Table 1. [113] [114] The physical properties of the samples that had been prepared in the foregoing

Examples and Comparative Examples were evaluated by the following methods, and evaluation results are represented in Table 1. [115] (1) Conversion ratio: A polymerization degree of the monomer except for a composition of nonvolatile materials was measured after measuring the total solid content of the sample. [116] - Total solid content

[117] = (weight of sample after drying / weight of sample before drying) x 100

[118] - Conversion ratio

[119] = [(total solid content - nonvolatile material content) x total]/total monomer weight

[120] (2) Particle diameter of rubber: A volume average particle diameter of the rubber was measured using a particle size measuring instrument A380 manufactured by

Nicomp Corporation. [121] (3) Notched izod impact strength (kgf-D/D): The notch Izod impact strength was measured at a thickness of 1/4" according to ASTM D256. [122] (4) Flow index (g/10 min): The melt flow index was measured according to ASTM

D1238.

[123] (5) Yellow index: the yellow index was measured according to ASTM D 1925.

[124] (6) Pencil hardness: The pencil hardness was measured by applying 500 g load 5 times to a surface of a test sample having a size of 3 mm (thickness) x 10 mm (length) x 6 mm (width) according to JIS (Japanese Industry Standard) K5401 at 23 ⁰ C. The surface of the sample is visually checked for scratches. If scratches are observed in two or more, the test is repeated with a pencil of one grade lower hardness. The results were classified into 4B~4H. [125] (7) Rubbing characteristics: After repeatedly rubbing the sample with a towel 1000 times, a scratch degree on the surface was observed by the naked eye (© excellent > O good > δ deteriorative > ▲ bad).

[126] (8) Transparency was measured by a color computer measuring instrument manufactured by Suga Instrument Corporation, and its measurement results were represented by a total light transmittance and a haze. [127] - Total light transmittance (%)

[128] = (light transmitted at all forward angles through a specimen) / (incident light through a specimen) x 100

[129] - Haze (%) [130] = (diffused transmission light) / (total light transmittance) x 100 [131] [132] Table 1

[133] [134] As shown in Table 1, it can be observed that Examples 1, 2 and 3 in which the impact modifier is introduced have improved impact resistances and excellent surface scratch resistances without greatly deteriorated transparency and haze characteristics as compared with PMMA of Comparative Example 7 with no impact modifier used. It can be confirmed that Comparative Example 1, in which diene-based monomer and alkyl acrylate ranges deviated from the ranges of the present invention, has deteriorated transparency and yellow index and its scratch resistance also dropped rapidly. It can be seen that Comparative Example 2, in which a rubber to MMA ratio deviated from the range of the present invention, has deteriorated transparency, yellow index and also flowability.

[135] It can be seen that Comparative Example 3 in which an average particle diameter of the rubber polymer deviated from the range of the present invention has deteriorated impact resistance. It can be confirmed that Comparative Example 4 has lowered yellow index and transparency and also deteriorated rubbing characteristics.

[136] It can be observed that Comparative Example 5, in which the cross-linking agent content deviated from the range of the present invention, has lowered impact strength

and also deteriorated scratch resistance and transparency. Further, it can be confirmed that Comparative Example 6, in which an anti-oxidant is not used during the polymerization, is not suitable for the present invention since yellow index is high.

[137]

[138] According to the present invention, it will be easily understood by those skilled in the art that simple modifications and changes can be made thereto. Also, such modifications and changes are encompassed within the scope of the present invention.