WO2010059008A2

WO2010059008A2 - Conductive resin composition including carbon composite

Info

Publication number: WO2010059008A2
Application number: PCT/KR2009/006909
Authority: WO
Inventors: 정만우; 전성윤; 한주희; 오주석; 이진서; 도승회; 홍성철
Original assignee: 한화석유화학 주식회사
Priority date: 2008-11-24
Filing date: 2009-11-24
Publication date: 2010-05-27
Also published as: TW201035996A; TWI406301B; WO2010059008A3

Abstract

The present invention relates to a conductive resin composition including a carbon composite, and more specifically to a polymer composition having a carbon composite which is economical and highly conductive. The polymer composition is a conductive resin composition comprising: 100 wt parts of a thermoplastic resin; 0.1–5 wt parts of a carbon nano tube that has undergone surface modification with respect to 100 wt parts of the thermoplastic resin; and 1–20 wt parts of a carbon compound with respect to 100 wt parts of the thermoplastic resin. The present invention also relates to a conductive resin composition with excellent foaming properties by further comprising 0.01–5 wt parts of a foaming agent with respect to 100 wt parts of the thermoplastic resin.

Description

Conductive Resin Compositions Including Composite Carbon Materials

The present invention relates to a highly conductive polymer mixture comprising a composite carbon material and to a polymer composition comprising a composite carbon material having excellent economic and conductivity.

Thermoplastic resins are excellent in processability and formability, and are widely applied to various household goods, office automation equipment, electrical and electronic products, and the like. Moreover, according to the kind and the characteristic of the product in which such a thermoplastic resin is used, in addition to the said excellent workability and moldability, the attempt to add a special property to a thermoplastic resin and to use it as a high value-added material is continuously made.

Among these, many attempts have been made to impart electrical conductivity to thermoplastic resins, and to use such electrically conductive thermoplastic resins for applications such as automobiles, various electrical devices, electronic assemblies, or cables to exhibit electromagnetic shielding performance.

Such electrically conductive thermoplastic resins are typically prepared using an electrically conductive thermoplastic resin composition in which a thermoplastic resin is mixed with a conductive additive such as carbon black, carbon fiber, metal powder, metal coated inorganic powder or metal fiber. By the way, it is difficult to ensure the electrical conductivity of the electrically conductive thermoplastic resin sufficiently to a desired degree unless a substantial amount of the conductive additive is added.

In addition, in the case of a polymer composite using carbon materials such as carbon black or carbon fiber, high hardness of the resin, surface roughness, and physical property deterioration are caused due to the input of a large amount of inorganic material, and it is difficult to realize the required high conductivity.

In addition, due to the additives added, there is a disadvantage in that foaming is not performed well when preparing expanded polymers.

On the other hand, there has been an attempt to impart excellent electrical conductivity to the electrically conductive thermoplastic resin using carbon nanotubes as the conductive additive.

However, when carbon nanotubes are mixed with the thermoplastic resin and injected to obtain the electrically conductive thermoplastic resin, the shear stress generated during the injection processing causes the agglomeration or orientation of the carbon nanotubes, and the carbon nanotubes in the electrically conductive thermoplastic resin appear. As the tubes are poorly dispersed, it is difficult to achieve the desired degree of electrical conductivity.

In Korean Patent Inventive No. 706652, 80 to 99 parts by weight of a thermoplastic resin; 0.1 to 10 parts by weight of carbon nanotubes; And it has been proposed an electrically conductive thermoplastic resin composition comprising 0.1 to 10 parts by weight of the organic nanoclay.

Further, according to Korean Patent Publication No. 2006-52657, A) 99. 6 to 10 parts by weight of at least one thermoplastic resin, B) 0 to 50 parts by weight of at least one rubber-elastic polymer, C) 0.2 to 10.0 parts by weight of carbon nano A composition has been proposed comprising fibrils, D) from 0.2 to 10.0 parts by weight of at least one particulate carbon compound, preferably carbon black or graphite powder, E) from 0 to 50 parts by weight of at least one filler and / or reinforcing material.

However, the patented method is still difficult to disperse the carbon nanotubes in the resin in order to maximize the performance of the carbon nanotubes, and a large amount of carbon nanotubes must be added to demonstrate the conductivity, so that the existing carbon black or carbon fiber There is a problem that the consumption of expensive raw materials is more expensive than using carbon materials, such as the economy.

In order to solve the above problems, an object of the present invention is to provide a polymer composition having excellent dispersibility, high conductivity, and economical efficiency by complexing a surface-modified carbon nanotube and another carbon compound to improve dispersibility. In addition, the present invention provides a polymer composition having excellent impact mitigation properties.

The present invention 100 parts by weight of thermoplastic resin to achieve the above object; 0.1 to 5.0 parts by weight of surface-modified carbon nanotubes based on 100 parts by weight of the thermoplastic resin; It provides a conductive resin composition comprising; and 1 to 20 parts by weight of the carbon compound with respect to 100 parts by weight of the thermoplastic resin. In another aspect, the present invention provides a conductive resin composition further comprises 0.01 to 5 parts by weight of the blowing agent relative to 100 parts by weight of the thermoplastic resin.

In addition, the present invention is the surface-modified carbon nanotube is a conductive resin that is surface-modified to include 0.1 to 10 parts by weight of an element selected from the group consisting of oxygen, nitrogen and mixtures thereof with respect to 100 parts by weight of carbon nanotubes To provide a composition.

In addition, the surface-modified carbon nanotubes of the present invention provides a conductive resin composition obtained by oxidation of a carbon nanotube surface by adding carboxylic acid, nitric acid, phosphoric acid or sulfuric acid to the carbon nanotubes.

In addition, the surface-modified carbon nanotubes of the present invention using a oxidizing agent selected from oxygen, air, ozone, hydrogen peroxide, nitric acid, nitro compounds and mixtures thereof, at a pressure of 50 to 400 atm and a temperature of 100 to 600 ° C. It provides a conductive resin composition obtained by oxidizing the carbon nanotube surface in the counting or supercritical water conditions.

In addition, the surface-modified carbon nanotubes of the present invention using a oxidizing agent selected from oxygen, air, ozone, hydrogen peroxide, nitric acid, nitro compounds and mixtures thereof, at a pressure of 50 to 400 atm and a temperature of 100 to 600 ° C. The carbon nanotube surface is oxidized under counting or supercritical conditions, followed by carboxyl, carboxyl salt, amine, amine salt, tetravalent-amine, phosphate group, phosphate, sulfate group, sulfate, alcohol, thiol, ester, amide, epoxide A functional compound having at least one functional group selected from the group consisting of side, aldehyde, ketone, and mixtures thereof is injected into a surface reforming reaction tank at a pressure of 50 to 400 atm and a temperature of 100 to 600 ° C. to provide a conductive resin composition obtained by surface treatment. .

In the present invention, the thermoplastic resin is a polyacetal resin, acrylic resin, polycarbonate resin, styrene resin, polyester resin, vinyl resin, polyphenylene ether resin, polyolefin resin, acrylonitrile-butadiene-styrene copolymer Resin, polyarylate resin, polyamide resin, polyamideimide resin, polyarylsulfone resin, polyetherimide resin, polyethersulfone resin, polyphenylene sulfide resin, fluorine resin, polyimide resin, polyetherketone resin, Polybenzoxazole resin, polyoxadiazole resin, polybenzothiazole resin, polybenzimidazole resin, polypyridine resin, polytriazole resin, polypyrrolidine resin, polydibenzofuran resin, polysulfone resin, polyurea resin, One resin, two or more copolymers selected from the group consisting of polyphosphazene resins and liquid crystal polymer resins It provides a resin or a mixture of two or more of the conductive resin composition.

In addition, the present invention provides a conductive resin composition containing carbon black, graphite or carbon fiber as the carbon compound.

In another aspect, the present invention provides a conductive resin composition having an average particle diameter of 0.001㎛ ~ 300㎛.

In another aspect, the present invention provides a molding prepared by extruding the conductive resin composition.

In another aspect, the present invention provides a plastic molding capable of flexibly varying the surface resistance of the molding, electromagnetic shielding, electrostatic dispersion and antistatic.

Hereinafter, a preferred embodiment of the present invention to the present invention will be described in detail. In describing the present invention, detailed descriptions of related well-known functions or configurations are omitted in order not to obscure the subject matter of the present invention.

As used herein, the terms “about”, “substantially”, and the like, are used at, or in close proximity to, numerical values when manufacturing and material tolerances inherent in the meanings indicated are intended to aid the understanding of the invention. Accurate or absolute figures are used to assist in the prevention of unfair use by unscrupulous infringers.

According to the present invention, by using a composite material of carbon nanotubes and a carbon compound modified in a thermoplastic resin, by using a surface-modified carbon nanotubes to improve dispersibility, an effect of increasing conductivity and a large amount of expensive carbon nanotubes is achieved. In order to compensate for the economic effects of using carbon nanotubes, the functionalities of carbon blacks, carbon black, graphite, and carbon fibers, which can support them, are used together with surface-modified carbon nanotubes. It is intended to extend the applicability of the conductive composition by providing synergy to provide functionality and economy. In addition, the present invention is intended to expand the applicability of the conductive composition exhibiting impact relaxation (buffering) with the addition of an excellent blowing agent and an excellent conductivity.

The present invention 100 parts by weight of thermoplastic resin; 0.1 to 5.0 parts by weight of surface-modified carbon nanotubes based on 100 parts by weight of the thermoplastic resin; It provides a conductive resin composition comprising; and 1 to 20 parts by weight of the carbon compound with respect to 100 parts by weight of the thermoplastic resin. The present invention also relates to a conductive resin composition further comprising 0.01 to 5 parts by weight of the blowing agent based on 100 parts by weight of the thermoplastic resin.

The thermoplastic resin used in the present invention is polyacetal resin, acrylic resin, polycarbonate resin, styrene resin, polyester resin, vinyl resin, polyphenylene ether resin, polyolefin resin, acrylonitrile-butadiene-styrene copolymer resin , Polyarylate resin, polyamide resin, polyamideimide resin, polyarylsulfone resin, polyetherimide resin, polyethersulfone resin, polyphenylene sulfide resin, fluorine resin, polyimide resin, polyetherketone resin, poly Benzoxazole resin, polyoxadiazole resin, polybenzothiazole resin, polybenzimidazole resin, polypyridine resin, polytriazole resin, polypyrrolidine resin, polydibenzofuran resin, polysulfone resin, polyurea resin, poly One resin, two or more copolymers selected from the group consisting of phosphazene resins and liquid crystal polymer resins Resins or mixtures of two or more may be used. Polyolefin resin or polyester resin is preferable, and polyethylene is more preferable among them.

In addition, the surface-modified carbon nanotubes of the present invention may be used as 0.1 to 5.0 parts by weight of surface-modified carbon nanotubes based on 100 parts by weight of the thermoplastic resin. The surface modified carbon nanotubes of the present invention can make excellent balance between mechanical properties and electrical conductivity. If the surface-modified carbon nanotubes are used at less than 0.1 part by weight, the effect of improving conductivity is insignificant. If the surface-modified carbon nanotubes are used in excess of 5.0 parts by weight, the mechanical properties of the thermoplastic resin may be deteriorated. This results in expensive raw material waste.

Carbon nanotubes of the present invention is composed of a single-walled, double walled, thin multi-walled, multi-walled, bundled and mixtures thereof Any form selected from the group is possible.

In addition, the surface-modified carbon nanotubes of the present invention is preferably surface-modified to include 0.1 to 10 parts by weight of a material selected from the group consisting of oxygen, nitrogen and mixtures thereof with respect to 100 parts by weight of carbon nanotubes.

The surface-modified carbon nanotubes through the oxidation have a significantly higher dispersibility in mixing with the resin and affect the conductivity. In addition, mixing with not only the resin but also other carbon materials or carbon compounds is facilitated.

Therefore, the surface-modified carbon nanotubes of the present invention include a method of causing oxidation of a surface by adding an acid, a method of oxidizing a surface of a carbon nanotube by reactivity of water under high temperature and high pressure.

For example, the surface-modified carbon nanotube of the present invention is oxygen, air, ozone, hydrogen peroxide, nitric acid, nitro compounds And oxidizing the surface of the carbon nanotubes under subcritical water or supercritical water conditions at a pressure of 50 to 400 atm and a temperature of 100 to 600 ° C. using an oxidant selected from a mixture thereof. Environmentally friendly surface modified carbon nanotubes can be obtained using oxidants that are not harmful in subcritical or supercritical conditions and are easy to handle and treat in wastewater. The surface modification of the subcritical water or supercritical water condition is that the oxidant is easily introduced to increase the surface modification effect of the carbon nanotubes, thereby increasing the dispersibility.

In addition, the surface-modified carbon nanotubes are subcritical water or supercritical water at a pressure of 50 to 400 atm and a temperature of 100 to 600 ° C. using an oxidant selected from oxygen, air, ozone, hydrogen peroxide, nitric acid, nitro compounds, and mixtures thereof. The carbon nanotube surface is oxidized under counting conditions, followed by carboxyl, carboxyl salt, amine, amine salt, tetra-amine, phosphate group, phosphate, sulfate group, sulfate, alcohol, thiol, ester, amide, epoxide, aldehyde And functional compounds having at least one functional group selected from the group consisting of ketones and mixtures thereof may be obtained by injecting a surface treatment reactor at a pressure of 50 to 400 atm and a temperature of 100 to 600 ° C.

In another example, the surface-modified carbon nanotubes may be obtained by adding carboxylic acid, nitric acid, phosphoric acid, or sulfuric acid to the carbon nanotubes by oxidation of the surface of the carbon nanotubes. Oxidation can be provided.

The carbon compound used in the present invention may be included as 1 to 20 parts by weight of the carbon compound based on 100 parts by weight of the thermoplastic resin. If the carbon compound is less than 1 part by weight, there is no effect of economical supplementation due to the addition of the carbon compound, and if it exceeds 20 parts by weight, there is no synergistic effect of the excess amount or conductivity.

The carbon compound may be used as long as the carbon compound includes carbon black, graphite or carbon fiber, and is not limited thereto.

In addition, in the case of carbon black, the carbon compound may have an average particle diameter of 0.001 to 0.5 µm, and graphite may have an average particle diameter of 1 to 300 µm in powder form. Moreover, the carbon fiber is also preferably a fine fiber having an average particle diameter of 0.01 to 0.1 mu m.

In addition to the carbon compound, the present invention may be used by mixing a carbon composite material with a conductive additive such as metal powder, metal coated inorganic powder, or metal fiber, and more preferably, lead (Pb), aluminum ( Al) metal powder can be used.

In addition, the present invention may further comprise 0.01 to 5 parts by weight of the blowing agent with respect to 100 parts by weight of the thermoplastic resin, the blowing agent is a component that can improve the conductivity, azodicarboxyamide, azobistetrazoldiaminoguanidine, azo Selected from bistetrazoleguanidine, 5-phenyltetrazole, bistetrazoleguanidine, bistetrazole piperazine, bistetrazolediammonium, N, N-dinitrosopentamethylenetetramine, hydrazodicarboxyamide and mixtures thereof Can be appropriately selected according to the thermoplastic resin. In the present invention, by using the foaming agent in 0.01 to 5 parts by weight, the dispersibility is good together with the surface-modified carbon nanotubes and the carbon compound, it is possible to excellently improve the conductivity and at the same time forming a good foam (foam) without trouble.

The present invention can be prepared by a known method by mixing the respective conductive resin compositions. The mixing of each of these components can be made into pellets by conventional extrusion, which can be used for various purposes, and the prepared pellets can be made into moldings to suit the purpose of sheets, films and the like.

The present invention is a conductive paint, electrostatic dispersion material, electrostatic dispersion paint, conductive material, electromagnetic wave shielding material, electromagnetic wave absorbing material, electromagnetic wave shielding paint, electromagnetic wave absorbing paint, solar cell material, dye-sensitized battery (DSSC) electrode material, electric device, electronic device , Semiconductor device, optoelectronic device, notebook component material, computer component material, mobile phone component material, PDA (PDA) component material, game machine component material, housing material, transparent electrode material, opaque electrode material, field emission display ( Field emission display (FED) materials, back light unit (BLU) materials, liquid crystal display (LCD) materials, plasma display panel (PDP) materials, light emitting diodes (LED) ) Materials, touch panel materials, billboard materials, billboard materials, display materials, heating elements, radiators, plating materials, catalysts, promoters, oxidants, reducing agents, automotive parts materials, ship parts Materials, aircraft component materials, electronic envelope materials, protective tape materials, adhesive materials, tray materials, clean room materials, transportation equipment component materials, flame retardant materials, antibacterial materials, metal composite materials, nonferrous metal composite materials, medical device component materials, One or more from the group consisting of building materials, flooring materials, wallpaper materials, light source component materials, lamp materials, optical component component materials, textile manufacturing component component materials, garment manufacturing component component materials, electrical appliance manufacturing equipment materials and electronic manufacturing equipment materials It relates to a conductive resin composition comprising a composite carbon material, characterized in that used for the selected material.

As described above, the conductive resin composition including the composite carbon material of the present invention has excellent conductivity by using a surface-modified carbon nanotube and a carbon compound such as graphite, carbon black, and carbon fiber together as a composite material, and a small amount. The use of carbon nanotubes has an economic effect of showing high conductivity. In addition, the resin composition further includes a foaming agent and has good foaming property, and exhibits excellent buffering effect due to excellent foaming, and has an excellent impact relaxation effect with conductivity. In addition, the conductive resin composition of the present invention has the effect of showing high conductivity even when using a small amount of expensive carbon nanotubes.

In addition, the carbon nanotubes of the present invention by using the surface-modified carbon nanotubes in subcritical water or supercritical water conditions to exclude the use of acids to facilitate the surface modification under environmentally friendly conditions and improve the dispersibility with the resin There is.

In addition, the conductive resin including the composite carbon material of the present invention is produced by the pellets has the effect of extending the applicability according to the application.

Through the following examples will be described in more detail.

Preparation Example 1

MWCNT solution was prepared in a pretreatment tank by mixing 12 g of Multi Wall Carbon Nano Tube (hereinafter referred to as MWCNT) (HANWHA NANOTECH, product name: CM95) with 988 g of distilled water and a circulation pump. Before the MWCNT solution is introduced into the preheater at a flow rate of 30 g / min through a high pressure injection pump, the oxygen in the gaseous state compressed to 245 atm to 252 atm is mixed with the MWCNT solution at a flow rate of 0.8 g / min at the front end of the heat exchanger The mixed solution was added to a preheating tank preheated to 200 to 260 ° C. through a heat exchanger. The preheated mixed solution is injected into a surface reforming reactor in a subcritical water state of 350 ° C. and 230 atm to 250 atm, and the surface modified product is transferred to a heat exchanger, and then first cooled to 200 ° C., and then again through a cooling device. After cooling to a temperature of about 25 ℃ to obtain a surface-modified continuously 11.8g multilayer carbon nanotubes.

Preparation Example 2

Except for using air instead of oxygen as the oxidizing agent was prepared in the same manner as in Preparation Example 1.

Preparation Example 3

Except for using ozone instead of oxygen as the oxidizing agent was prepared in the same manner as in Preparation Example 1.

Preparation Example 4

It was prepared in the same manner as in Preparation Example 1, except that 108.8 g (1.6 M) of 50% hydrogen peroxide aqueous solution was added instead of oxygen as the oxidizing agent.

Preparation Example 5

It was prepared in the same manner as in Preparation Example 1, except that 25.2 g (0.4 M) of nitric acid was added instead of oxygen as the oxidizing agent.

Example 1

Into a hopper of a rotating twin screw extruder, 940 g of low density polyethylene (LDPE 830; HCC), 10 g of surface modified carbon nanotubes (MWCNT) of Preparation Example 1, and 50 g of carbon black (VXC500; CABOT) were added. Rotation of the extruder shaft at 200 ° C. melted the polymer resin at, kneaded with the carbon material and continuously exited through the extruder die. Polyethylene strands exiting the extruder were made into conventional short pellets using a pelletizer, and then the pellets were made into a sheet having a thickness of 2 mm using a press.

Example 2

Into the hopper of the twin screw extruder, 905 g of low density polyethylene (LDPE 830; HCC), 5 g of surface modified carbon nanotube (MWCNT) of Preparation Example 2, and 90 g of carbon black (VXC500; CABOT) were added. Except that, it was carried out in the same manner as in Example 1.

Example 3

Instead of the surface-modified carbon nanotubes of Preparation Example 1 was carried out in the same manner as in Example 1, except that 10g of the surface-modified carbon nanotubes of Preparation Example 3, 50g of carbon fibers having an average particle diameter of 0.1㎛ instead of 50g of carbon black. .

Example 4

Instead of the surface-modified carbon nanotubes of Preparation Example 1 was carried out in the same manner as in Example 2, except that 5g of the surface-modified carbon nanotubes of Preparation Example 4, 90g of carbon fibers having an average particle diameter of 10.0㎛ instead of carbon black 90g. .

Example 5

Instead of the surface-modified carbon nanotubes of Preparation Example 1 was carried out in the same manner as in Example 2 except that 5g of the surface-modified carbon nanotubes of Preparation Example 5, 90g of carbon fibers having an average particle diameter of 10.0㎛ instead of 90g of carbon black. .

Example 6

938 g of low density polyethylene (LDPE 830; HCC), 10 g of carbon nanotubes (MWCNT) of Preparation Example 1, 50 g of carbon black (VXC500; CABOT), and 2 g of azodicarboxyamide were added to a hopper of a rotating twin screw extruder. . The polymer resin was melted and kneaded with the carbon material by the rotating screw in the extruder maintained at 150 ° C. to continuously eject the sheet through the extruder die. This sheet was placed in an oven at 200 ° C. to obtain a foam sheet.

Example 7

903 g of low density polyethylene (LDPE 830; HCC), 5 g of carbon nanotube (MWCNT) of Preparation Example 2, and 90 g of carbon black (VXC500; CABOT) were added to the hopper of the twin screw extruder. , The same as in Example 6.

Example 8

The carbon nanotubes of Preparation Example 1 were used in the same manner as in Example 6 except that 10g of carbon nanotubes of Preparation Example 3 and 50g of carbon fibers having an average particle diameter of 0.1 μm were used instead of 50g of carbon black.

Example 9

Instead of the carbon nanotubes of Preparation Example 1 was carried out in the same manner as in Example 7, except that 5g of carbon nanotubes of Preparation Example 4 and 90g of carbon black instead of 90g of carbon black.

Example 10

The carbon nanotubes of Preparation Example 1 were used in the same manner as in Example 7, except that 5g of the carbon nanotubes of Preparation Example 5 and 90g of carbon fibers having an average particle diameter of 10.0 μm were used instead of 90g of carbon black.

Comparative Example 1

970 g of low density polyethylene (LDPE 830; HCC) and 30 g of unmodified carbon nanotubes (MWCNT) of Preparation Example 1 were added to a hopper of a rotating twin screw extruder. Rotation of the extruder shaft at 200 ° C. melted the polymer resin at, kneaded with the carbon material and continuously exited through the extruder die. Polyethylene strands exiting the extruder were made into conventional short pellets using a pelletizer, and then the pellets were made into a sheet having a thickness of 2 mm using a press.

Comparative Example 2

Except for using the surface-modified carbon nanotubes of Preparation Example 1 instead of the surface-modified carbon nanotubes were carried out in the same manner as in Comparative Example 1.

Comparative Example 3

The same procedure was followed as in Comparative Example 1 except that 650 kg of low density polyethylene (LDPE830; HCC) and 350 g of carbon black (VXC500; CABOT) were added to a hopper of a rotating twin screw extruder.

Comparative Example 4

The same procedure was followed as in Comparative Example 1 except that 750 g of low density polyethylene (LDPE830; HCC) and 250 g of carbon fiber having an average particle diameter of 0.1 μm were added to a hopper of a rotating twin screw extruder.

Comparative Example 5

Except for using surface-modified carbon nanotubes 5g unmodified carbon nanotubes (MWCNT) was carried out in the same manner as in Example 1.

Comparative Example 6

The same procedure as in Example 2 was carried out except that 5 g of unmodified carbon nanotubes (MWCNT) were used instead of the surface modified carbon nanotubes.

Comparative Example 7

The same procedure as in Example 3 was carried out except that 10 g of unmodified carbon nanotubes (MWCNT) were used instead of the surface modified carbon nanotubes.

Comparative Example 8

Except for using surface-modified carbon nanotubes 5g unmodified carbon nanotubes (MWCNT) was carried out in the same manner as in Example 4.

Comparative Example 9

Same as Example 6, except that 968 g of low density polyethylene (LDPE 830; HCC), 30 g of unmodified carbon nanotube (MWCNT), and 2 g of azodicarboxyamide were added to the hopper of the rotating twin screw extruder. It was carried out.

Comparative Example 10

Except for using the surface-modified carbon nanotubes of Preparation Example 1 instead of the surface-modified carbon nanotubes were carried out in the same manner as in Comparative Example 9.

Comparative Example 11

The same procedure as in Comparative Example 9 was conducted except that 648 g of low density polyethylene (LDPE830; HCC) and 350 g of carbon black (VXC500; CABOT) were added to a hopper of a rotating twin screw extruder.

Comparative Example 12

The same procedure as in Comparative Example 9 was conducted except that 748 g of low density polyethylene (LDPE830; HCC) and 250 g of carbon fiber having an average particle diameter of 0.1 µm were added to a hopper of a rotating twin screw extruder.

Comparative Example 13

The same procedure as in Example 6 was conducted except that 5 g of unmodified carbon nanotubes (MWCNT) were used.

Comparative Example 14

The same procedure as in Example 7 was carried out except that 5 g of unmodified carbon nanotubes (MWCNT) were used.

Comparative Example 15

The same procedure as in Example 8 was conducted except that 10 g of unmodified carbon nanotubes (MWCNT) were used.

Comparative Example 16

The same procedure as in Example 9 was carried out except that 5 g of unmodified carbon nanotubes (MWCNT) were used.

Comparative Example 17

The same procedure as in Example 6 was carried out except that low density polyethylene (LDPE 830; HCC) was adjusted to 940 g without using azodicarboxyamide.

*Test Methods

1. Surface Resistance Measurement

It was measured according to JISK 7194 / ASTM D991 using Mitsubishi's Loresta GP (MCP-T600).

TABLE 1

TABLE 2

The present invention described above is not limited to the above-described embodiments and the accompanying drawings, and various substitutions, modifications, and changes can be made without departing from the technical spirit of the present invention. It will be evident to those who have knowledge of.

Claims

100 parts by weight of thermoplastic resin;

0.1-5 parts by weight of surface-modified carbon nanotubes; And

1 to 20 parts by weight of carbon compound;

Conductive resin composition comprising a.
The method of claim 1,

The conductive resin composition further comprises 0.01 to 5 parts by weight of a blowing agent based on 100 parts by weight of the thermoplastic resin.
The method according to claim 1 or 2,

The surface-modified carbon nanotubes are surface-modified conductive resin composition such that 0.1 to 10 parts by weight of an element selected from the group consisting of oxygen, nitrogen, and mixtures thereof, based on 100 parts by weight of carbon nanotubes.
The method of claim 3,

The surface-modified carbon nanotubes are oxygen, air, ozone, hydrogen peroxide, nitric acid, nitro compounds And a conductive resin composition obtained by oxidizing a carbon nanotube surface under subcritical water or supercritical water conditions at a pressure of 50 to 400 atm and a temperature of 100 to 600 ° C. using an oxidant selected from a mixture thereof.
The method of claim 3,

The surface-modified carbon nanotubes are subcritical water or supercritical condition at a pressure of 50 to 400 atm and a temperature of 100 to 600 ° C. using an oxidant selected from oxygen, air, ozone, hydrogen peroxide, nitric acid, nitro compounds, and mixtures thereof. Oxidation of the surface of the carbon nanotubes, followed by carboxyl, carboxyl salt, amine, amine salt, tetra-amine, phosphate group, phosphate, sulfate group, sulfate, alcohol, thiol, ester, amide, epoxide, aldehyde, ketone And a conductive resin composition obtained by surface treatment by injecting a functional compound having at least one functional group selected from the group consisting of a mixture thereof into a surface reforming reaction tank at a pressure of 50 to 400 atm and a temperature of 100 to 600 ° C.
The method of claim 3,

The surface-modified carbon nanotubes are obtained by adding a carboxylic acid, nitric acid, phosphoric acid or sulfuric acid to the carbon nanotubes by oxidation of the surface of the carbon nanotubes.
The method according to claim 1 or 2,

The thermoplastic resin is polyacetal resin, acrylic resin, polycarbonate resin, styrene resin, polyester resin, vinyl resin, polyphenylene ether resin, polyolefin resin, acrylonitrile-butadiene-styrene copolymer resin, polyarylate Resin, polyamide resin, polyamideimide resin, polyarylsulfone resin, polyetherimide resin, polyethersulfone resin, polyphenylene sulfide resin, fluorine-based resin, polyimide resin, polyetherketone resin, polybenzoxazole resin, Polyoxadiazole resin, polybenzothiazole resin, polybenzimidazole resin, polypyridine resin, polytriazole resin, polypyrrolidine resin, polydibenzofuran resin, polysulfone resin, polyurea resin, polyphosphazene resin and One resin, two or more copolymer resins or two selected from the group consisting of liquid crystal polymer resins Mixture of conductive resin composition on the.
The method according to claim 1 or 2,

The carbon compound is a conductive resin composition selected from the group consisting of carbon black, graphite, carbon fibers and mixtures thereof.
The method of claim 8,

The carbon compound is a conductive resin composition having an average particle diameter of 0.001㎛ ~ 300㎛.
The method of claim 2,

The blowing agent is azodicarboxyamide, azobistetrazoldiaminoguanidine, azobistetrazolguanidine, 5-phenyltetrazole, bistetrazolguanidine, bistetrazolpiperazine, bistrezazolediammonium, N, N-di A conductive resin composition selected from nitrosopentamethylenetetramine, hydrazodicarboxyamide and mixtures thereof.
The method according to claim 1 or 2,

The conductive resin composition may include conductive paints, electrostatic dispersion materials, electrostatic dispersion paints, conductive materials, electromagnetic wave shielding materials, electromagnetic wave absorbing materials, electromagnetic wave shielding paints, electromagnetic wave absorbing paints, solar cell materials, dye-sensitized battery (DSSC) electrode materials, electrical devices, Electronic device, semiconductor device, optoelectronic device, notebook component material, computer component material, mobile phone component material, PDA (PDA) component material, game machine component material, housing material, transparent electrode material, opaque electrode material, field emission Field emission display (FED) materials, back light unit (BLU) materials, liquid crystal display (LCD) materials, plasma display panel (PDP) materials, light emitting diodes (LEDs); luminescent diode) materials, touch panel materials, billboard materials, billboard materials, display materials, heating elements, radiators, plating materials, catalysts, promoters, oxidants, reducing agents, automotive parts Materials, ship parts materials, aircraft parts materials, electronic envelope materials, protective tape materials, adhesive materials, tray materials, clean room materials, transportation equipment parts materials, flame retardant materials, antibacterial materials, metal composite materials, nonferrous metal composite materials, medical Consists of device component materials, building materials, flooring materials, wallpaper materials, light source component materials, lamp materials, optical equipment component materials, textile manufacturing equipment component materials, garment manufacturing equipment component materials, electrical appliance manufacturing equipment materials and electronic manufacturing equipment materials A conductive resin composition comprising a composite carbon material, characterized in that it is used in at least one material selected from the group.
A molded article prepared by extruding the conductive resin composition of claim 1.
The method of claim 12,

The molding is a plastic molding capable of shielding electromagnetic waves, electrostatic dispersion or antistatic by controlling the surface resistance.