KR20110078521A - Polycarbonate resin composition having good flame retardancy - Google Patents

Abstract

PURPOSE: A polycarbonate resin composition is provided to ensure environment-friendliness while maintaining excellent flame retardancy and heat resistance and to enable the application to the molded products of electric/electronic materials. CONSTITUTION: A polycarbonate resin composition includes 100 parts by weight of a base resin and 0.1~40 parts by weight of a phosphorus compound. The phosphorus compound includes a phosphate-based compound represented by chemical formula 2 and a phosphate-based compound represented by chemical formula 3. The base resin comprises 30~99 weight% of a polycarbonate resin and 1~70 weight% of a rubber-modified aromatic vinyl resin.

Description

Polycarbonate Resin Composition Having Good Flame Retardancy

The present invention relates to a polycarbonate resin composition excellent in flame retardancy. More specifically, the present invention relates to a thermoplastic resin composition having excellent flame resistance and excellent heat resistance by applying a combination of two phosphorus compounds to a base resin of a polycarbonate resin and a rubber-modified aromatic vinyl resin as a flame retardant.

Recently, the use of plastic polymers or synthetic resins has been diversified, such as vehicles, building materials, aircraft, railways, and home appliances, and as the development of various functional additives is rapidly progressing, its application range is explosively increasing. However, the plastic itself has the property of easy combustion and is not resistant to fire. Therefore, the plastic can be easily burned by the external ignition source, and can serve to spread the fire further. In light of this, countries such as the US, Japan, and Europe regulate the use of polymer resins that meet the flame retardant standards to ensure the safety of fires in electronic products.

Flame retardant methods of polymers include a method of synthesizing a thermally stable resin through design or molecular structure design, a method of chemically improving a conventional polymer (reactive type), a method of physically adding a flame retardant by blending or compounding. (Additive type), a method of coating or painting a flame retardant. The most widely known flame retardant method is to add a flame retardant to the polymer resin. Additive flame retardants are classified into halogen-based, phosphorus-based, nitrogen-based, silicon-based and inorganic flame-retardants depending on the constituents.

Halogen-based flame retardant plays a role of suppressing the chain reaction of the combustion process through the reaction with radicals generated in the gas phase during the combustion process of the polymer in the resin. As the halogen compound, polybromodiphenyl ether, tetrabromobisphenol A, brominated substituted epoxy compound and chlorinated polyethylene are mainly used, and antimony trioxide and antimony pentoxide are mainly used as the antimony compound. Bromine-based flame retardants are the most widely used because of their unique properties, price, and excellent flame retardancy, especially in the electrical and electronics fields, but environmental issues continue to be discussed. As a result, in July 2006, the RoHS (Restriction of Use of Hazardous Substances in Electrical and Electronic Products) came into effect, and as a result, some of the general-purpose bromine-based flame retardants, also called deca, have been discontinued.

Phosphorus-based flame retardants have recently emerged as a representative non-halogen flame retardant that can respond to environmental regulations as an environmentally friendly flame retardant. Phosphorus-based flame retardants exhibit excellent flame retardant effects in solid phase reactions and are particularly effective for plastics containing large amounts of oxygen. Phosphorus-based flame retardants are classified into phosphates, phosphine oxides, phosphites, phosphonates, and the like and achieve flame retardancy by using char forming agents such as polycarbonate resins or polyphenylene ether resins. As the phosphorus compound, aromatic phosphate esters such as triphenyl phosphate and resorcinol bisphenol phosphate are mainly used.

U.S. Patent 4,692,488 discloses thermoplastic resin compositions consisting of non-halogen aromatic polycarbonate resins, non-halogen styrene-acrylonitrile copolymers, non-halogen phosphorus compounds, tetrafluoroethylene polymers and small amounts of ABS copolymers. U.S. Patent No. 5,061,745 discloses flame retardant resin compositions composed of aromatic polycarbonate resins, ABS graft copolymers, styrenic copolymers, phosphate esters and tetrafluoroethylene polymers. However, there is a problem in that a certain amount or more must be added in order to exhibit an effect of flame retardancy by adding phosphate ester.

Accordingly, the present inventors added an phosphorous compound using a mixture of phosphate and phosphonate as a flame retardant to a basic resin composed of a polycarbonate resin and a rubber-modified aromatic vinyl resin, thereby exhibiting excellent flame resistance and excellent heat resistance. It is early to develop.

An object of the present invention is to provide a polycarbonate resin composition excellent in flame retardancy.

Another object of the present invention is to provide a polycarbonate resin composition having excellent heat resistance as well as flame retardancy.

Another object of the present invention is to provide an environmentally friendly flame retardant polycarbonate resin composition.

Still another object of the present invention is to provide a flame retardant polycarbonate resin composition which is excellent in flame retardancy and can be applied as a molded article of an electric / electronic material.

The above and other objects of the present invention can be achieved by the present invention described below.

In order to solve the above technical problem, the polycarbonate resin composition according to the present invention 100% by weight of the base resin containing (A) 30 to 99% by weight of polycarbonate resin and (B) 1 to 70% by weight of rubber modified aromatic vinyl resin 0.1-40 weight part of phosphorus compounds which consist of (C) (C1) phosphate type compound and (C2) phosphonate type compound with respect to a part.

In one embodiment of the present invention, the phosphorus compound (C) is (C1) 20 to 80% by weight of the phosphate compound represented by the formula (2); And (C2) 20 to 80 wt% of the phosphonate compound represented by the formula (3).

In another embodiment of the present invention, the phosphorus content of the phosphorus compound (C) is 0.8 to 1.1 wt%.

In another embodiment of the present invention, the resin composition may further include additives such as flame retardants, lubricants, plasticizers, heat stabilizers, anti-drip agents, antioxidants, compatibilizers, light stabilizers, pigments, dyes, inorganic additives. .

In order to solve the said another technical subject, this invention provides the molded article manufactured from the said resin composition.

The present invention has the effect of providing an environmentally friendly thermoplastic resin composition while maintaining excellent flame retardancy by applying two kinds of phosphorus compounds to polycarbonate resin and rubber-modified aromatic vinyl resin.

Hereinafter, the present invention will be described in more detail.

The polycarbonate resin composition of the present invention is based on 100 parts by weight of the base resin containing (A) 30 to 99% by weight of the polycarbonate resin and (B) 1 to 70% by weight of the rubber-modified aromatic vinyl resin, (C) (C1 A phosphorus compound comprising 0.1 to 40 parts by weight of a phosphate compound and a (C2) phosphonate compound.

(A) polycarbonate resin

Polycarbonate resin composition according to an embodiment of the present invention can be produced by a method known to those skilled in the art, or commercially available polycarbonate resin can be used without limitation.

For example, the polycarbonate resin may be prepared by reacting a diphenol compound represented by Chemical Formula 1 with phosgene, halogen formate, or carbonic acid diester.

[Formula 1]

Wherein A represents a single bond, C ₁ -C ₅ alkylene, C ₁ -C ₅ alkylidene, C ₅ -C ₆ cycloalkylidene, -S- or -SO _2-

Specific examples of the diphenol compound of Formula 1 include hydroquinone, resorcinol, 4,4'-dihydroxydiphenyl, 2,2-bis- (4-hydroxyphenyl) -propane, 2,4-bis- (4-hydroxyphenyl) -2-methylbutane, 1,1-bis- (4-hydroxyphenyl) -cyclohexane, 2,2-bis- (3-chloro-4-hydroxyphenyl) -propane, 2,2-bis- (3,5-dichloro-4-hydroxyphenyl) -propane, and the like, and the like. Among these, 2,2-bis- (4-hydroxyphenyl) -propane, 2,2-bis- (3,5-dichloro-4-hydroxyphenyl) -propane, 1,1-bis- (4- Preference is given to using hydroxyphenyl) -cyclohexane and the like, more preferably 2,2-bis- (4-hydroxyphenyl) -propane, also called bisphenol-A (Bisphenol-A, BPA). The polycarbonate resin of the present invention preferably has a weight average molecular weight (M _w ) of 10,000 to 200,000 g / mol, more preferably 15,000 to 80,000 g / mol.

As the polycarbonate, not only linear polycarbonate resins, but also branched polycarbonate resins or polyester-carbonate resins may be used without limitation. At this time, the branched polycarbonate may be prepared by adding 0.05-2 mol% of trivalent or more polyfunctional compounds, such as compounds having trivalent or more phenol groups, based on the total amount of diphenol compounds.

As the polycarbonate used in the production of the resin composition of the present invention, homopolycarbonate or gecko polycarbonate can be used without limitation, and it is also possible to use it in the form of a blend of homo polycarbonate and copolycarbonate.

In addition, the polycarbonate used in the preparation of the resin composition of the present invention may be partially or entirely replaced by an aromatic polyester-carbonate resin obtained by polymerizing in the presence of an ester precursor, for example, a bifunctional carboxylic acid. It is possible.

The polycarbonate resin (A) content used in the flame retardant polycarbonate resin composition of the present invention is 30 to 30 of the base resins (A) + (B) made of polycarbonate resin (A) 'and rubber-modified aromatic vinyl resin (B). 99% by weight, preferably 40 to 90% by weight, more preferably 50 to 80% by weight, still more preferably 60 to 77% by weight. When applied within the above range, excellent flame retardancy and mechanical property balance can be obtained.

(B) rubber modified aromatic vinyl resin

Rubber-modified aromatic vinyl resins are polymers in which rubber polymers are dispersed and present in the form of particles in a matrix form (continuous phase) made of an aromatic vinyl polymer.

The rubber-modified aromatic vinyl resin may be prepared by adding an aromatic vinyl monomer and a copolymerizable vinyl monomer therein in the presence of a rubbery polymer. Such rubber-modified aromatic vinyl resins can be produced by known polymerization methods such as emulsion polymerization, suspension polymerization, and bulk polymerization.

Typically, a rubber-derived graft copolymer resin and a rubber-containing copolymer resin are separately prepared, and then the mixture is extruded to prepare a rubber-modified aromatic vinyl resin. However, in the case of the bulk polymerization, the rubber-modified aromatic vinyl resin can be prepared in one step reaction process without separately preparing the graft copolymer resin and the copolymer resin.

In any of the above polymerization methods, the rubber content in the final rubber-modified aromatic vinyl resin component is 1 to 30% by weight, preferably 3 to 20% by weight, and more preferably 5 to 15% by weight, based on the entire base resin. %to be. The rubber particle size is 0.1-6.0 μm in Z-average, preferably 0.25-4 μm. Examples of such resins include acrylonitrile-butadiene-styrene copolymer resins (ABS), acrylonitrile-acryl rubber-styrene copolymer resins (AAS), acrylonitrile-ethylenepropylene rubber-styrene copolymer resins (AES) , Rubber reinforced polystyrene (HIPS), and the like. They can also be applied in mixtures of two or more.

The rubber-modified aromatic vinyl resin may be applied in combination of graft resin alone or graft copolymer resin and copolymer resin, and is preferably blended in consideration of their compatibility. More specifically, 10-100 wt% of graft copolymer resin (B ₁ ) and copolymer resin (B ₂ ) in rubber-modified aromatic vinyl resins  It is preferable to mix | blend 0 to 90 weight%. In an embodiment, the rubber-modified aromatic vinyl resin (B) may be blended with 55 to 90 wt% of the graft copolymer resin (B ₁ ) and 10 to 45 wt% of the copolymer resin (B ₂ ). In another embodiment, the rubber-modified aromatic vinyl resin (B) may be blended with 15 to 50 wt% of the graft copolymer resin (B ₁ ) and 50 to 85 wt% of the copolymer resin (B ₂ ).

The content of the rubber-modified aromatic vinyl resin (B) used in the flame retardant polycarbonate resin composition of the present invention is 1 to 70% by weight of the base resin (A) + (B), preferably 1 to 50% by weight. More preferably 5 to 40% by weight.

Hereinafter, the graft copolymer resin (B ₁ ) and the copolymer resin (B ₂ ) which are components of the rubber-modified aromatic vinyl resin (B) according to the present invention will be described in detail.

(B ₁ ) graft copolymer resin

The graft copolymer resin (B ₁ ) used in the present invention is produced by polymerizing an aromatic vinyl monomer capable of graft copolymerization with a rubbery polymer and a monomer copolymerizable with the aromatic vinyl monomer.

Examples of the rubber used for the graft copolymer resin include diene rubbers such as polybutadiene, poly (styrene-butadiene) and poly (acrylonitrile-butadiene), saturated rubbers hydrogenated with the diene-based rubber, isoprene rubber, Acrylic rubber such as chloroprene rubber and butyl polyacrylate, ethylene-propylene rubber, ethylene-propylene-diene monomer terpolymer (EPDM) and the like. The rubber may be used alone or in combination of two or more thereof. Among these, "diene-based" rubber is preferred, and more preferably butadiene-based rubber is suitable. The content of rubber is suitably 5 to 65 weight percent of the total weight of the graft copolymer resin. The average particle size of the rubber particles is in the range of 0.1 to 4 μm in consideration of the impact strength and appearance.

The aromatic vinyl monomers include styrene monomers such as styrene, α-methylstyrene, β-methylstyrene, p-methylstyrene, para t-butylstyrene, ethyl styrene, monochlorostyrene, dichlorostyrene, dibromostyrene, and the like. It can be used representatively. The styrene monomers may be used alone or in combination of two or more thereof. Of these, styrene is most preferred. The content of the aromatic vinyl monomer is 34 to 94% by weight of the graft copolymer resin.

One or more monomers copolymerizable with the aromatic vinyl monomers may be introduced. As a monomer which can be introduce | transduced, an unsaturated nitrile type compound like acrylonitrile and methacrylonitrile is preferable. The unsaturated nitrile compound may be used alone or in combination of two or more thereof. The content of the copolymerizable monomer may be used in 1 to 30% by weight of the graft copolymer resin.

In the preparation of the graft copolymer, monomers such as acrylic acid, methacrylic acid, maleic anhydride, and N-substituted maleade may be further added to give graft polymerization properties such as processability and heat resistance. Monomers adding the processability and heat resistance may be used alone or in combination of two or more thereof. The added content is in the range of 0 to 15 weight percent of the total graft copolymer resin.

(B ₂ ) copolymer resin

The copolymer resin of the present invention is polymerized in consideration of compatibility in a content equivalent to the monomer ratio excluding rubber among the components of the graft copolymer.

Examples of the aromatic vinyl monomer used in the copolymer resin include styrene, α-methylstyrene, β-methylstyrene, p-methylstyrene, para t-butylstyrene, ethyl styrene, monochlorostyrene, dichlorostyrene and dibromostyrene. Etc. Styrene-based monomers may be used, but are not necessarily limited thereto. Of these, styrene is most preferred. These can be used individually or in mixture of 2 or more types. The addition amount of the aromatic vinyl monomer in the copolymer resin is preferably 60 to 90% by weight.

As a monomer copolymerizable with the said aromatic aromatic vinyl monomer, an unsaturated nitrile type compound like acrylonitrile and methacrylonitrile is preferable. The unsaturated nitrile compound may be used alone or in combination of two or more thereof. The content of the copolymerizable monomer may be used in 10 to 40% by weight of the total weight of the graft copolymer resin.

In addition, in order to impart properties such as processability and heat resistance, the copolymers may be copolymerized by adding monomers such as acrylic acid, methacrylic acid, maleic anhydride, and N-substituted maleade by adding 0-30 wt% to the total weight of the copolymer resin. Can be.

(C) phosphorus compounds

Phosphorus-based flame retardants exhibit excellent flame retardant effects in solid phase reactions and are particularly effective for plastics containing large amounts of oxygen. In the present invention, by using a mixture of two kinds of phosphorus compounds with respect to the thermoplastic resin composition gives excellent flame retardancy compared to the single application. Phosphorus compounds (C1) and (C2) are for imparting flame retardancy of the present invention and have structures represented by the following formulas (2) and (3). Phosphorus compound (C1) is a phosphate type compound, (C2) is a phosphonate type compound. Each phosphorus compound is used in combination to provide synergistic effect in application, providing excellent flame resistance and high heat resistance. Phosphorus-based compound (C) of the present invention can be easily prepared by those skilled in the art. The phosphorus compound (C) is (C1) 20 to 80% by weight of a phosphate compound represented by the following formula (2); And (C2) 20 to 80% by weight of a phosphonate compound represented by the following Chemical Formula 3, where each component is as follows.

(C1) phosphate compounds

[Formula 2]

(In Formula 2, R ₁ , R ₂ , R ₃ , R ₄ , R ₅ , R ₆ are each independently hydrogen or an alkyl group of C ₁ -C ₄ , X is an aryl group or alkyl group of C ₆ -C ₂₀ Substituted C ₆ -C ₂₀ aryl group derived from dialshol of resorcinol, hydroquinol, bisphenol-A, n ranges from 0 to 4)

In the present invention, the phosphate compound (C1) may be used alone or as a mixture of two or more kinds, and constitutes 20 to 80% by weight, preferably 30 to 70% by weight of the phosphorus compound (C). When used in less than 20% by weight, the flame retardancy and heat resistance of the resin composition is poor. On the other hand, when it exceeds 80 weight%, the mechanical strength of a resin composition falls.

(C2) phosphonate compound

(3)

(In Formula 3, R ₁ is independently an C ₁ -C ₁₀ alkyl group, an aryl group or an aryl group substituted with an alkyl group, an aralkyl group.)

In the present invention, the phosphonate compound (C2) may be used alone or as a mixture of two or more kinds, and constitutes 20 to 80% by weight, preferably 30 to 70% by weight of the phosphorus compound (C).

In the specific example of this invention, it is preferable that the phosphorus compound (C) of this invention contains 0.8-1.1 weight% of phosphorus in all the phosphorus compounds (C). In case of applying phosphorus compound (C) having a phosphorus content of less than 0.8 wt%, sufficient physical properties such as flame retardancy cannot be secured, and in the case of applying phosphorus compound (C) having a phosphorus content of more than 1.1 wt%, due to excessive input of a flame retardant. There is a problem that the impact strength is lowered.

In an embodiment of the present invention, the phosphorus compound (C) is applied by mixing (C1) and (C2) and the total content of (C1) and (C2) is 0.1 to 40 parts by weight, based on 100 parts by weight of the base resin, It is preferably used in an amount of 1 to 30 parts by weight, more preferably 2 to 20 parts by weight. When the phosphorus-based compound (C) is used in less than 0.1 parts by weight, there is a problem that can not ensure sufficient flame retardancy, while when used in excess of 40 parts by weight there is a problem that mechanical properties such as impact strength is lowered Not .

In an embodiment of the present invention, the polycarbonate resin composition may further include an additive according to each use. As the additive, a flame retardant, lubricant, plasticizer, heat stabilizer, anti-drip agent, antioxidant, compatibilizer, light stabilizer, pigment, dye, inorganic additive, and the like may be used, but are not necessarily limited thereto. These can be used individually or in mixture of 2 or more types. Preferred examples of the inorganic additives include asbestos, glass fibers, talc, ceramics or sulfates.

The additive may be used in an amount of 30 parts by weight or less, preferably 0.1 to 30 parts by weight, based on 100 parts by weight of the base resin.

The polycarbonate resin composition according to the present invention can be produced by a known method for producing a resin composition. For example, the components of the present invention and other additives may be mixed at the same time and then melt-extruded in an extruder to produce pellets or chips.

Since the polycarbonate resin composition of the present invention is excellent in flame retardancy and excellent in heat resistance, for example, TV, audio, cell phone, digital camera, navigation, washing machine, computer, monitor, MP3, video player, CD player, It can be widely used in housing of electrical and electronic products such as washing machines, office automation equipment and other large injection molding products.

There is no particular limitation on the method of molding the plastic molded article using the polycarbonate resin composition according to the present invention, and for example, an extrusion, injection or casting molding method may be applied. The molding can be easily carried out by those skilled in the art to which the present invention pertains.

The present invention may be further embodied by the following examples, which are only specific examples of the present invention, and are not intended to limit or limit the protection scope of the present invention.

Example

The specification of each component used in the following Examples and Comparative Examples is as follows.

(A) polycarbonate resin

PANLITE L-1250W manufactured by Teijin, Japan was used as a bicarbonate-type polycarbonate having a weight average molecular weight of 25,000 g / mol.

(B) rubber modified aromatic vinyl resin

CHT, a rubber-reinforced styrene resin of Cheil Industries, Inc., was used.

(C) phosphorus compounds

(C1) phosphate compounds

(C1-a) Dihatch's PX200 was used.

(C1-b) An RDP from Dihatch was used.

(C1-c) Phosphate in which R ₂ is a tert-butyl group was used.

(C2) phosphonate compound

(C2-a) A phosphonate in which R ₁ is a phenyl group was used.

(C2-b) A phosphonate in which R ₁ is a benzyl group was used.

Examples 1-6 and Comparative Examples 1-3

The pellets were prepared by extruding the components in a temperature range of 200˜280 ° C. using a conventional twin screw extruder in a content such as Tables 1 and 2 below. The prepared pellets were dried at 80 ° C. for 2 hours, and then injected into a 10-ounce injection machine under conditions of a molding temperature of 180 to 280 ° C. and a mold temperature of 40 to 80 ° C. to prepare a specimen.

Property evaluation method

(1) Flame retardancy: evaluated by using a specimen of 1/8 '' thickness according to the UL 94 VB flame retardant standard.

(2) Total combustion time: The sum of both primary and secondary combustion times for five specimens for flame retardancy evaluation.

(3) Heat resistance: VST (Vicat Softening Temperature) was weighted at 5 kg according to ISO R 306.

(4) IZOD impact strength: measured in accordance with ASTM D-256 specification at 1/8 "thickness (kgfcm / cm).

Comparative Example One 2 3 (A) polycarbonate resin 70 70 70 (B) rubber modified aromatic vinyl resin 30 30 30 (C) take over
compound (C1) phosphate (C1-a) 8 - - (C1-b) - 8 - (C1-c) - - 8 (C2) phosphonate (C2-a) - - - (C2-b) - - - Phosphorus content (% by weight) 0.67 0.72 0.56 Total burning time (s) - - - UL-94 Fail Fail Fail Heat resistance degree (℃) 111 108 104 IZOD impact strength 23 21 20

As shown in Table 1, Examples 1 to 6 in which the phosphate-based compound (C1) and the phosphonate-based compound (C2) of the phosphorus-based compound were used in combination with each other. It can be seen that the flame retardancy, impact strength and heat resistance at 1/8 "thickness are more excellent.

Simple modifications and variations of the present invention can be easily made by those skilled in the art, and all such modifications or changes can be seen to be included in the scope of the present invention.

Claims (9)

(A) 30 to 99% by weight of a polycarbonate resin; And (B) 1 to 70% by weight of the rubber-modified aromatic vinyl resin; With respect to 100 parts by weight of the base resin containing the (A) + (B), 0.1 to 40 parts by weight of a phosphorus compound composed of (C) (C1) a phosphate compound represented by Formula 2 below and (C2) a phosphonate compound represented by Formula 3 below; A polycarbonate resin composition having excellent flame retardancy, comprising: [Formula 2]

In Formula 2, R ₁ , R ₂ , R ₃ , R ₄ , R ₅ , and R ₆ are each independently hydrogen or an alkyl group of C ₁ -C ₄ , and X is an aryl group or alkyl group of C ₆ -C ₂₀ . C ₆ -C ₂₀ aryl group derived from dialshol of resorcinol, hydroquinol, bisphenol-A, n ranges from 0 to 4 (3)

R ₁ in Formula 3 is independently an alkyl group, an aryl group or an aryl group substituted with an alkyl group, an aralkyl group of C ₁ -C ₁₀ . The method of claim 1, wherein the rubber modified aromatic vinyl resin (B) is (B ₁ ) 5 to 65% by weight of the rubbery polymer, 34 to 94% by weight of the aromatic vinyl monomer, 1 to 30% by weight of the monomer copolymerizable with the aromatic vinyl monomer, and 0 to monomer which adds processability and heat resistance. 10 to 100% by weight of the graft copolymer resin graft polymerized 15% by weight; And (B ₂ ) 60 to 90% by weight of an aromatic vinyl monomer, 10 to 40% by weight of a monomer copolymerizable with the aromatic vinyl monomer, and 0 to 30% by weight of a copolymer resin which adds processability and heat resistance. Polycarbonate resin composition excellent in flame retardancy, characterized in that consisting of 90% by weight. The method of claim 2, wherein the aromatic vinyl monomer is styrene, α-methylstyrene, β-methylstyrene, p-methylstyrene, para t- butyl styrene, ethyl styrene, monochloro styrene, dichloro styrene, dibromo styrene and A polycarbonate resin composition excellent in flame retardancy, characterized in that it is selected from the group consisting of these mixtures. The polycarbonate resin composition having excellent flame retardancy according to claim 2, wherein the monomer copolymerizable with the aromatic vinyl monomer is an unsaturated nitrile compound. The polycarbonate resin composition having excellent flame retardancy according to claim 2, wherein the monomer adding processability and heat resistance is selected from the group consisting of acrylic acid, methacrylic acid, maleic anhydride, N-substituted maleade, and mixtures thereof. . The method of claim 1, wherein the phosphorus compound (C) is (C1) 20 to 80% by weight of the phosphate compound represented by the formula (2); And (C2) 20 to 80% by weight of a phosphonate compound represented by Chemical Formula 3, wherein the polycarbonate resin composition has excellent flame retardancy. The polycarbonate resin composition having excellent flame retardancy according to claim 1, wherein the phosphorus content of the phosphorus compound (C) is 0.8 to 1.1 wt%. The method of claim 1, wherein the resin composition further comprises at least one additive selected from the group consisting of flame retardants, flame retardant aids, lubricants, plasticizers, heat stabilizers, anti-drip agents, antioxidants, compatibilizers, light stabilizers, pigments, dyes and inorganic additives. Thermoplastic resin composition excellent in the flame retardancy characterized by including. The molded article manufactured from the resin composition of any one of Claims 1-8.