JP5163597B2 - Non-halogen flame retardant resin composition, method for producing the same, and electric wire / cable using the same - Google Patents

Description

  The present invention relates to a non-halogen flame retardant resin composition that forms a dispersed phase in an olefin-based resin matrix by using a dynamic crosslinking technique, and in particular, a continuous silane-crosslinked ethylene-vinyl acetate copolymer as a dispersed phase. The present invention relates to a non-halogen flame-retardant resin composition obtained by using an ethylene-ethyl acrylate copolymer as a phase and highly filling a flame retardant, a method for producing the same, and an electric wire / cable using the same.

  Awareness of environmental problems is increasing worldwide, and non-halogen flame retardant resins that do not generate harmful gases during combustion and that can be recycled are becoming widespread.

  Various halogen-free flame retardant resins have been developed so far. For example, as shown in Patent Documents 1 and 2, an olefin-based resin which is a fluid component is used as a matrix by using a dynamic crosslinking technique, and the matrix There is a technique for dispersing olefinic rubber and the like inside.

  In general, non-halogen highly flame-retardant resins used for insulating materials for electric wires and cables need to be highly filled with metal hydroxides such as aluminum hydroxide and magnesium hydroxide.

JP-A-11-228750 JP 2008-31354 A

  However, a non-halogen flame retardant resin highly filled with a metal hydroxide has a poor melt flow property, so that a high torque is applied during extrusion processing, and high speed extrusion becomes difficult. Not only that, the elongation decreases significantly. In applications where heat resistance is required, such as for electric wires for equipment, it is necessary to improve resistance to heat deformation and cut-through by crosslinking with an electron beam. Inferior.

  Therefore, the object of the present invention is to solve the above-mentioned problems and to form a silane-crosslinked ethylene-vinyl acetate copolymer as a dispersed phase when forming a dispersed phase in an olefin resin matrix using a dynamic crosslinking technique. By using an ethylene-ethyl acrylate copolymer as a continuous phase, it has high mechanical strength and heat resistance without cross-linking with an electron beam, and can be extruded at high speed even when highly filled with a flame retardant, and is good The present invention provides a non-halogen flame retardant resin composition exhibiting elongation, a production method thereof, and an electric wire / cable using the same.

  In order to achieve the above object, the invention of claim 1 is as follows: (A) ethylene-vinyl acetate copolymer 40-80 parts by mass, (B) ethylene-ethyl acrylate copolymer 60-20 masses having a melting point of 100 ° C. or higher. Part, (C) the metal hydroxide consists of 20 to 300 parts by mass with respect to 100 parts by mass in total of (A) and (B), and the ethylene-vinyl acetate copolymer (A) is silane-crosslinked This is a halogen-free flame retardant resin composition.

  The invention of claim 2 is characterized in that the phase of (A) ethylene-vinyl acetate copolymer is dispersed in the phase of (B) ethylene-ethyl acrylate copolymer having a melting point of 100 ° C. or higher. The non-halogen flame retardant resin composition according to claim 1.

  The invention according to claim 3 is the non-halogen flame retardant resin composition according to claim 1 or 2, wherein the metal hydroxide (C) is magnesium hydroxide and is surface-treated with a silane coupling agent. .

  Invention of Claim 4 WHEREIN: The said (C) metal hydroxide is 200-300 mass parts with respect to a total of 100 mass parts of (A) and (B), The halogen-free flame retardant of Claim 1 or 2 It is an adhesive resin composition.

According to a fifth aspect of the present invention, there is provided a method for producing the non-halogen flame retardant resin composition according to any one of the first to fourth aspects, wherein the silane-crosslinked ethylene-vinyl acetate copolymer is grafted with a silane compound. It is a method for producing a halogen-free flame retardant resin composition, which is formed by kneading a polymerized ethylene-vinyl acetate copolymer, a metal hydroxide and a silanol condensation catalyst.

  The invention according to claim 6 is the halogen-free flame retardant resin composition according to claim 5, wherein the ethylene-vinyl acetate copolymer is graft copolymerized with a silane compound, and then the ethylene-ethyl acrylate copolymer and the metal hydroxide are added. It is a manufacturing method of a thing.

The invention of claim 7, the non-halogen flame retardant resin composition according to any one of claims 1 to 4, a wire or cable characterized in that it uses an insulator or sheath.

  According to the present invention, a non-halogen flame-resistant material that has high mechanical strength and heat resistance without cross-linking with an electron beam after cable formation, can be extruded at high speed even when highly filled with a flame retardant, and exhibits good elongation. The excellent effect that a flammable resin composition can be obtained is exhibited. Moreover, since it is not cross-linked with an electron beam, it is excellent in recyclability.

It is detailed sectional drawing of the electric wire and cable to which this invention is applied. It is detailed sectional drawing of the electric wire and cable to which this invention is applied. It is a figure which shows an example of the manufacturing apparatus used for the manufacturing method of the electric wire and cable which concerns on this invention.

  A preferred embodiment of the present invention will be described below in detail with reference to the accompanying drawings.

  First, an electric wire / cable to which the present invention is applied will be described with reference to FIGS.

  In FIG. 1, a copper conductor 1 is coated with an insulator 2 made of a halogen-free flame retardant resin composition to form an electric wire 5, and three wires 5 are twisted together. An electric wire / cable 4 formed by fully extruding the sheath 3 is shown.

  FIG. 2 shows an electric wire / cable 4 formed by extruding the sheath 3 into a tube shape on the outer periphery of the three twisted electric wires 5.

  FIG. 3 shows an apparatus for producing an electric wire 5 by extruding an insulator 2 on a copper conductor 1 or producing an electric wire 5 by extruding a sheath 3 on a cable core 12 in which a plurality of electric wires 5 are twisted together. It is.

  In the figure, a cable core 12 comprising a copper conductor 1 and a twisted electric wire 5 is fed from an unwinding machine 11 to an extrusion die 13, while the non-halogen flame retardant resin composition of the present invention is extruded from an extrusion machine 10 to an extrusion die 13. And is covered with the copper conductor 1 and the cable core 12 to be the electric wire 5 or the electric wire / cable 4. After being cooled in the cooling water tank 14, the electric wire 5 or the electric wire / The cable 4 is manufactured.

  The present invention provides a non-halogen flame retardant resin composition in which a silane cross-linked ethylene-vinyl acetate copolymer (A) is used as a disperse phase when a disperse phase is formed in an olefin resin matrix using a dynamic cross-linking technique. Without cross-linking with an electron beam by using an ethylene-ethyl acrylate copolymer (B) having a melting point of 100 ° C. or higher as a continuous phase and highly filling the flame retardant (C) metal hydroxide, Non-halogen flame retardant resin composition having high mechanical strength and heat resistance, capable of high-speed extrusion even when highly filled with a flame retardant, and exhibiting good elongation, a method for producing the same, and an electric wire / cable using the same It is what.

  The ethylene-vinyl acetate copolymer (A) defined in the present invention is not particularly limited in terms of molecular weight, melt viscosity and the like, and any one can be used.

  In addition, the (A) ethylene-vinyl acetate copolymer is copolymerized with a silane compound for silane crosslinking. Silane compounds are required to have both a group capable of reacting with a polymer and an alkoxy group that forms a crosslink by silanol condensation. Specifically, vinyltrimethoxysilane, vinyltriethoxysilane, vinyltris (β -Methoxyethoxy) silane and other vinylsilane compounds, γ-aminopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, N-β- (aminoethyl) γ-aminopropyltrimethoxysilane, β- (aminoethyl) γ- Aminosilane compounds such as aminopropylmethyldimethoxysilane, N-phenyl-γ-aminopropyltrimethoxysilane, β- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-glycid Xypropylmethyldiethoxy Epoxy silane compounds such as run, acrylic silane compounds such as γ-methacryloxypropyltrimethoxysilane, polysulfides such as bis (3- (triethoxysilyl) propyl) disulfide, bis (3- (triethoxysilyl) propyl) tetrasulfide Examples thereof include mercaptosilane compounds such as silane compounds, 3-mercaptopropyltrimethoxysilane, and 3-mercaptopropyltriethoxysilane.

  A known general method for graft copolymerization of a silane compound, that is, a predetermined amount of a silane compound and a free radical generator are mixed with a base ethylene-vinyl acetate copolymer and melt-kneaded at a temperature of 80 to 200 ° C. The method can be used.

  As the free radical generator, organic peroxides such as dicumyl peroxide can be mainly used.

  Although the addition amount of the silane compound is not particularly defined, 0.5 to 10 parts by mass is preferable with respect to 100 parts by mass of the ethylene-vinyl acetate copolymer in order to obtain good physical properties. If the amount is less than 0.5 parts by mass, a sufficient crosslinking effect cannot be obtained, and the strength and heat resistance of the composition are inferior. When it exceeds 10 mass parts, workability will fall remarkably.

  Moreover, the optimal amount of the organic peroxide which is a free radical generator is 0.001-3 mass parts with respect to 100 mass parts of ethylene-vinyl acetate copolymers. When the amount is less than 0.001 part by mass, the silane compound is not sufficiently graft copolymerized and a sufficient crosslinking effect cannot be obtained. If it exceeds 3 parts by mass, scorching of the ethylene-vinyl acetate copolymer tends to occur.

  (B) As the ethylene-ethyl acrylate copolymer having a melting point (Tm) of 100 ° C. or higher, a known one can be used. Here, an ethylene-ethyl acrylate copolymer having a melting point (Tm) of less than 100 ° C. is not preferable because the heat shrinkage rate at 100 ° C. is increased and good characteristics cannot be obtained.

  By using an ethylene-ethyl acrylate copolymer having a melting point (Tm) of 100 ° C. or higher, the present invention can be suitably used for a cable that requires heat shrinkage resistance at 100 ° C. or higher. It is easy to process into an electric wire.

  In the present invention, the blending ratio of the (A) ethylene-vinyl acetate copolymer and the (B) ethylene-ethyl acrylate copolymer having a melting point of 100 ° C. or higher is such that (A) When the component (A) is 40 to 80 parts by mass and (B) is 60 to 20 parts by mass, the tensile strength is significantly reduced. On the other hand, when the amount of the component (A) is less than 40 parts by mass, the elongation characteristics are remarkably deteriorated, and good flexibility cannot be obtained.

  The (C) metal hydroxide used in the present invention imparts flame retardancy in the composition and promotes crosslinking of the ethylene-vinyl acetate copolymer obtained by graft copolymerization with the silane compound together with the silanol condensation catalyst. And enables cross-linking during kneading.

  Although the details of the mechanism for promoting crosslinking are unknown, it is speculated that the water content of the metal hydroxide promotes hydrolysis of the alkoxy group, and the silanol condensation catalyst promotes dehydration condensation of the silanol group. .

  Examples of such metal hydroxides include magnesium hydroxide, aluminum hydroxide, calcium hydroxide, and the like. Among them, magnesium hydroxide having the highest flame retardant effect is preferable. The metal hydroxide is preferably surface-treated from the dispersibility parent point.

  As the surface treatment agent, a silane coupling agent, a titanate coupling agent, a fatty acid, a fatty acid metal salt, or the like can be used, and among them, a silane coupling agent is preferable in terms of improving the adhesion between the resin and the metal hydroxide.

  Examples of silane coupling agents that can be used include vinylsilane compounds such as vinyltrimethoxysilane, vinyltriethoxysilane, and vinyltris (β-methoxyethoxy) silane, γ-aminopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, N- aminosilane compounds such as β- (aminoethyl) γ-aminopropyltrimethoxysilane, β- (aminoethyl) γ-aminopropylmethyldimethoxysilane, N-phenyl-γ-aminopropyltrimethoxysilane, β- (3,4 Epoxycyclohexyl) Epoxysilane compounds such as ethyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-glycidoxypropylmethyldiethoxysilane, and acrylic silanization such as γ-methacryloxypropyltrimethoxysilane , Polysulfide silane compounds such as bis (3- (triethoxysilyl) propyl) disulfide, bis (3- (triethoxysilyl) propyl) tetrasulfide, 3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane, etc. And mercaptosilane compounds.

  As a method of treating these surface treatment agents with a metal hydroxide, known methods such as a wet method, a dry method, and a direct kneading method may be used.

  The surface treatment amount is not particularly specified, but it is preferably in the range of 0.1 to 5 mass% with respect to the metal hydroxide. If the surface treatment amount is less than 0.1 mass%, the strength of the resin composition decreases. And when more than 5 mass%, workability will worsen.

  The average particle diameter of the metal hydroxide is more preferably 4 μm or less from the viewpoint of mechanical properties, dispersibility, and flame retardancy.

  (C) The addition amount of the metal hydroxide is 20 to 20 parts by mass with respect to a total of 100 parts by mass of (A) an ethylene-vinyl acetate copolymer and (B) an ethylene-ethyl acrylate copolymer having a melting point of 100 ° C. or higher. 300 parts by mass. If the amount is less than 20 parts by mass, the flame retardant effect cannot be obtained. However, if the amount is 20 parts by mass or more, the characteristics of the 60-degree inclined flame test of the flame retardant test (1) are high. VW-1 characteristics of the flammability test (2) can be satisfied. If it exceeds 300 parts by mass, the moldability is remarkably lowered and kneading becomes impossible.

  In the present invention, an unsaturated carboxylic acid or a derivative thereof is copolymerized with (A) a part of the ethylene-vinyl acetate copolymer or (B) a part of the ethylene-ethyl acrylate copolymer having a melting point of 100 ° C. or higher. It is possible to use an ethylene-vinyl acetate copolymer or an ethylene-ethyl acrylate copolymer. That is, (C) an ethylene-vinyl acetate copolymer or an ethylene-ethyl acrylate copolymer obtained by copolymerizing a metal hydroxide and an unsaturated carboxylic acid or a derivative thereof can be used. As a result, a reaction occurs between (C) the metal hydroxide and the unsaturated carboxylic acid or derivative thereof, and the mechanical strength of the composition is improved by increasing the adhesion. As the ethylene-vinyl acetate copolymer or the ethylene-ethyl acrylate copolymer here, those described above can be used as they are. The unsaturated carboxylic acid or derivative thereof is not particularly limited, but maleic anhydride is preferred. The amount to be replaced is arbitrary, but 0.5 to 10 parts by mass is desirable. If the amount is less than 0.5 parts by mass, the effect of improving the strength cannot be obtained, and if it exceeds 10 parts by mass, the workability is remarkably lowered.

  Examples of the silanol condensation catalyst that can be used in the present invention include cibutyltin dilaurate, dibutyltin diacetate, dibutyltin dioctate, stannous acetate, stannous caprylate, zinc caprylate, lead naphthenate, cobalt naphthenate, and the like. The amount of addition depends on the type of catalyst, but is set to 0.001 to 0.1 parts by mass per 100 parts by mass in total of (A) and (B).

  As an addition method, there is a method of using a master batch previously mixed with (A) an ethylene-vinyl acetate copolymer or (B) an ethylene-ethyl acrylate copolymer, in addition to the method of adding as it is.

  In addition to the above, process oil, processing aid, flame retardant aid, crosslinking agent, crosslinking aid, antioxidant, lubricant, inorganic filler, compatibilizer, stabilizer, carbon black, colorant, etc. It is also possible to add other additives.

  Although there is no limitation in the apparatus which manufactures the composition of this invention, general purpose things, such as a kneader, a Banbury mixer, a roll, a twin screw extruder, can be used.

  Hereinafter, Examples 1 to 9 and Comparative Examples 1 to 7 of the present invention will be described together with Table 1.

  In Examples 1-9 and Comparative Examples 1-7, (A) an ethylene-vinyl acetate copolymer was graft copolymerized with a silane compound, and then an ethylene-ethyl acrylate copolymer (Examples 1-7, comparison) Examples 1-4, Comparative Example 6) or a step of kneading a polyolefin resin (Comparative Examples 5 and 6), and kneading compounding agents such as the kneaded product, metal hydroxide, silanol condensation catalyst, and ethylene-vinyl acetate. The copolymer was prepared by a silane crosslinking step.

  In the step of grafting the silane compound to the ethylene-vinyl acetate copolymer and then kneading the ethylene-ethyl acrylate copolymer or polyolefin resin, the raw material (A) ethylene-vinyl acetate copolymer (vinyl acetate) Content VA, 42 mass%) 30 to 90 parts by mass, vinyltrimethoxysilane 3.5 parts by mass, dicumyl peroxide 0.02 parts by mass, ethylene-ethyl acrylate copolymer or polyolefin resin (polypropylene, linear The low-density polyethylene was charged into a 40 mm twin screw extruder (L / D = 60) set at 206 ° C. in the range of 10 to 70 parts by mass.

  The ethylene-ethyl acrylate copolymer or polyolefin resin is introduced from the side after the grafting reaction of the ethylene-vinyl acetate copolymer by the silane compound proceeds.

  Next, (C) a metal hydroxide, a silanol condensation catalyst (dibutyltin laurate), and an antioxidant are introduced into a wonder kneader (55 L) so that the blending ratio shown in Table 1 is obtained. The kneaded product was prepared by crosslinking the ethylene-vinyl acetate copolymer that was kneaded and graft copolymerized during the kneading.

  The kneaded material, metal hydroxide prepared in the step of kneading the ethylene-ethyl acrylate copolymer after graft-copolymerizing the silane compound to the ethylene-vinyl acetate copolymer at a chamber temperature of 120 ° C. to 160 ° C. Are put into Wonder Nida at once. The metal hydroxide may be added separately or in a batch. In addition, when an activator such as polymethyl methacrylate or another flame retardant such as melamine cyanurate is added, it is added simultaneously with the metal hydroxide. After sufficiently kneading and dispersing, when the resin temperature reaches 140 ° C. to 150 ° C., a silanol condensation catalyst is added and kneaded to crosslink the ethylene-vinyl acetate copolymer with silane, and the resin temperature is 180 ° C. to 190 ° C. At the stage of reaching this point, this was pelletized and used as a material for cable production.

  The wires and cables were produced by extrusion coating the cable core to a thickness of 1.5 mm using a 40 mm extruder (L / D = 24) preheated to 180 ° C. As the cable core, a copper conductor having an outer diameter of 2 mm coated with polyethylene with a thickness of 0.8 mm was twisted with three cores together with interposition and wound with a kraft paper tape.

  The electric wires and cables produced by the above procedure were evaluated by the following method.

  For additional heat of winding, after winding the wire / cable 6 times around the tube of the wire / cable diameter and holding it at 121 ° C. for 1 hour, after confirming that there was no crack in the appearance observation, conduct an AC 1000V voltage test. Those without dielectric breakdown were considered acceptable.

  For low temperature winding, the cable was wound 6 times around a tube of twice the cable diameter and held at minus 10 ° C. for 4 hours, and then the cable having no cracks was accepted.

  Mechanical strength, heat resistance, oil resistance, and flame resistance were evaluated in accordance with JIS C3005. A tensile strength of 8.27 MPa or more and an elongation at break of 100% or more were considered acceptable.

  Heat deformation was evaluated by a heat deformation test (75 ° C., load 10 N), and a thickness reduction rate of 50% or less was accepted.

  For heat shrinkage, cut the produced wire / cable to a length of 1 m and hold it at 100 ° C. for 2 hours, then measure the length of the insulator protruding from the sheath, and the amount of protrusion of the insulator should be 3 mm or less at both ends. Passed.

  The heat resistance was determined to be acceptable if the tensile strength residual ratio was 75% or more after being held at 136 ° C. for 168 hours.

  For the flame retardancy evaluation, a flame retardancy test (1) a 60-degree inclined flame test and a higher flame retardancy test (2) VW-1 test were performed.

  (1) In the 60-degree inclined combustion test, the fire spread time after removing the flame was measured, and the fire extinguished naturally within 60 seconds was regarded as acceptable.

  (2) In the VW-1 test, the cable was placed vertically, flame was applied to the lower part of the cable for 15 seconds using methane gas, and after 60 seconds, the flame did not reach the flag 50 cm above the flash point and spontaneous digestion The test was repeated 5 times, and 5 times, natural digestion and those in which the flame did not reach the flag were accepted.

  In the above, as shown in Table 1, Examples 1 to 9 have good characteristics.

  In Comparative Example 1, the content of (C) metal hydroxide is 100 parts by mass in total of (A) an ethylene-vinyl acetate copolymer and (B) an ethylene-ethyl acrylate copolymer having a melting point of 100 ° C. or higher. On the other hand, it is a case of 10 parts by mass, and the flame retardant effect is not obtained. However, in Example 3, when the content of (C) metal hydroxide is 20 parts by mass, flame retardant (2) VW-1 Although the above characteristics are unacceptable, it is acceptable in the flame retardant (1) 60 degree oblique combustion test. Therefore, the content of (C) metal hydroxide is preferably 20 parts by mass or more.

  In Examples 4 to 6, the content of (C) the metal hydroxide was increased to 100, 200, and 300 parts by mass, but the flame retardancy (2) was achieved by setting the content to 200 to 300 parts by mass. The characteristics of VW-1 are acceptable. In particular, Example 6 can be kneaded even when the content of (C) the metal hydroxide is 300 parts by mass, and satisfies the properties of flame retardant (1) 60 degree oblique combustion test and (2) VW-1. However, in Comparative Example 2, the content of (C) the metal hydroxide is 350 parts by mass, and kneading is impossible, and (C) the metal hydroxide is (A) an ethylene-vinyl acetate copolymer. And (B) The moldability cannot be sufficiently dispersed and kneaded in the ethylene-ethyl acrylate copolymer, and the moldability is significantly reduced.

  Therefore, (C) 20 to 300 parts by mass of the metal hydroxide is preferable when more flame resistance is required for the electric wire / cable.

  Next, with respect to the mixing ratio of (A) ethylene-vinyl acetate copolymer and (B) ethylene-ethyl acrylate copolymer, Comparative Example 3 has 30 parts by mass for (A) and 70 parts by mass for (B). Although the elongation and the heat deformation are poor, in Example 1, (A) is 40 parts by mass, (B) is 60 parts by mass, and the elongation and the heat deformation satisfy the regulations. Therefore, (A) ethylene- The vinyl acetate copolymer is preferably 40 parts by mass or more.

  In Comparative Example 4, (A) is 90 parts by mass and (B) is 10 parts by mass. Among the characteristics, the tensile strength does not satisfy the regulation. In Example 2, (A) is 80 parts by mass, ( B) is 20 parts by mass, and the tensile strength satisfies the regulation.

  Therefore, (A) 40 parts by weight or more and 80 parts by weight or less of the ethylene-vinyl acetate copolymer is preferable.

  Next, Examples 7 and 8 are examples in which magnesium hydroxide and aluminum hydroxide were used as the (C) metal hydroxide, and both characteristics were satisfied. In Example 9, 5 parts by mass of polymethyl methacrylate was added as an activator, and high-speed extrudability comparable to that in Examples 3 and 4 with a small amount of metal hydroxide added was obtained.

  In Examples 1 to 9, the melting point of (B) ethylene-ethyl acrylate copolymer was 104 ° C and 100 ° C, whereas Comparative Example 7 had a melting point of 95 ° C and less than 100 ° C. In this example, an ethylene-ethyl acrylate copolymer is used, and the heat shrinkage at 100 ° C. increases and the thermal deformation increases.

  Therefore, the melting point of the (B) ethylene-ethyl acrylate copolymer is preferably 100 ° C. or higher.

  Comparative Examples 5 and 6 are examples in which polypropylene and linear low-density polyethylene were used instead of (B) ethylene-ethyl acrylate copolymer, both of which are elongations that are indicators of high-speed extrudability, Heat shrinkage was poor, and Comparative Example 5 failed in the additional heat of winding and low-temperature winding, and (2) VW-1 failed even when 200 parts by mass of metal hydroxide was added.

  Although each composition of the present invention has been described above, in addition to the composition of the resin composition according to the present invention described above, a process oil, a processing aid, a flame retardant aid, a crosslinking agent, a crosslinking aid, an oxidation as necessary. It is also possible to add additives such as inhibitors, lubricants, inorganic fillers, compatibilizers, stabilizers, carbon black, and colorants.

  In order to further improve the flame retardant effect, a flame retardant such as melamine cyanurate is kneaded or a phosphorus flame retardant is used as (A) an ethylene-vinyl acetate copolymer or (B) ethylene having a melting point of 100 ° C. or higher. It is also possible to graft the ethyl acrylate copolymer.

  In order to reduce the motor load of the kneader during kneading, as shown in Example 9, it is possible to knead an active agent such as polymethyl methacrylate. The polymethyl methacrylate is not particularly limited, but the average particle diameter is more preferably 10 μm or less in terms of mechanical properties and dispersibility, and the amount of polymethyl methacrylate added is (A) ethylene- 0.1-10 mass parts is suitable with respect to a total of 100 mass parts of a vinyl acetate copolymer and (B) ethylene-ethyl acrylate copolymer whose melting | fusing point is 100 degreeC or more.

1 Copper conductor 2 Insulator 3 Sheath 4 Electric wire / cable 5 Electric wire

Claims (7)

  (A) 40-80 parts by mass of an ethylene-vinyl acetate copolymer, (B) 60-20 parts by mass of an ethylene-ethyl acrylate copolymer having a melting point of 100 ° C. or higher, (C) a metal hydroxide with (A) A non-halogen flame retardant resin composition comprising 20 to 300 parts by mass per 100 parts by mass of (B), wherein the ethylene-vinyl acetate copolymer (A) is silane-crosslinked.   The non-halogen according to claim 1, wherein the phase of (A) ethylene-vinyl acetate copolymer is dispersed in the phase of (B) ethylene-ethyl acrylate copolymer having a melting point of 100 ° C or higher. Flame retardant resin composition.   The non-halogen flame retardant resin composition according to claim 1 or 2, wherein the metal hydroxide (C) is magnesium hydroxide and is surface-treated with a silane coupling agent.   The non-halogen flame retardant resin composition according to claim 1 or 2, wherein the (C) metal hydroxide is 200 to 300 parts by mass with respect to 100 parts by mass in total of (A) and (B). The method for producing the non-halogen flame retardant resin composition according to any one of claims 1 to 4 , wherein the silane-crosslinked ethylene-vinyl acetate copolymer is obtained by graft-copolymerizing a silane compound. A method for producing a non-halogen flame retardant resin composition, which is formed by kneading a copolymer, a metal hydroxide and a silanol condensation catalyst.   6. The method for producing a non-halogen flame retardant resin composition according to claim 5, wherein the silane compound is graft copolymerized with the ethylene-vinyl acetate copolymer, and then the ethylene-ethyl acrylate copolymer and the metal hydroxide are added. Wires and cables, characterized in that the halogen-free flame retardant resin composition according to any one of claims 1 to 4, used in the insulator or sheath.

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