KR100792233B1 - A microcellular foam of thermoplastic resin prepared with a die having improved cooling property - Google Patents

Abstract

The present invention relates to a micro-foam of a thermoplastic resin, and more particularly, to a micro-foam having a skin layer having a porosity of less than 5% and a core layer having a porosity of 5% or more, wherein the thickness of the skin layer is 5 to 50% of the total thickness. It is about.

Compared with the general microfoam, the microfoam of the present invention has a thicker skin layer, a smaller size of the micropores of the core layer, and a uniform distribution thereof, and thus exhibits similar mechanical properties to those of the conventional nonfoamed sheet.

Fine foam, polyvinyl chloride, skin layer, extrusion, cooling section

Description

A micro foam of a thermoplastic resin manufactured using a die having improved cooling performance {A MICROCELLULAR FOAM OF THERMOPLASTIC RESIN PREPARED WITH A DIE HAVING IMPROVED COOLING PROPERTY}

1 is a cross-sectional view showing an example of an extrusion die including a pressure drop section, a temperature change section, and a cooling section.

2 is a cross-sectional view showing an example of an extrusion die including a pressure drop section, a temperature change section, and a cooling section together, and including a plurality of cooling means and heating means.

Figure 3 is a block diagram showing the configuration of an extrusion apparatus for producing a micro-foam of the embodiment of the present invention.

Figure 4 is a cross-sectional view showing the configuration of an extrusion die for producing the micro-foam of Comparative Examples 1, and 2 of the present invention.

Figure 5 is a cross-sectional view showing the configuration of an extrusion die for producing a micro-foam of Comparative Example 3 of the present invention.

Figure 6 is a scanning electron micrograph of the fracture surface of the micro-foam sheet according to Example 1.

7 is a scanning electron micrograph of the fracture surface of the foam sheet according to Comparative Example 3.

[Industrial use]

The present invention relates to a micro-foam of the thermoplastic resin, and more particularly to a micro-foam of the thermoplastic resin having a mechanical property similar to the conventional non-foamed sheet at a low specific gravity.

[Private Technology]

Soundproofing, insulation, building materials, lightweight structural materials, packaging materials, insulating materials, cushioning materials, dustproof materials, shoes, etc. for the purpose of thermal insulation, sound absorption, buoyancy, elasticity, light weight, sound insulation, or by foaming plastics with foaming gas or foaming agents The foam may be prepared using a physical blowing agent or a chemical blowing agent.

Examples of physical blowing agents include carbon dioxide, nitrogen, or hydrofluorocarbons, and examples of chemical blowing agents may include gas generating organic materials such as azodicarbonamide.

According to US Pat. No. 6,225,365, chemical foaming agents reduce the physical properties of the final product because residues remain after decomposition, while physical foaming agents are free of residues to provide better foams. However, this foaming method tends to have low mechanical strength and toughness because the resulting pores are relatively large (about 100 μm or more) and have a high level of porosity (about 50% or more).

In order to solve this problem, an ultra-fine foaming method for producing a plastic foam having a high pore density and a small pore size has been developed, which is described in US Patent No. 4,473,665 (1984.09.25).

In addition, various methods have been proposed for continuously producing a foam material having a microstructure. US Patent No. 5,866,053 (1999.02.02) discloses a continuous method of forming microfoams. The invention is characterized by a rapid drop in the pressure of a single phase solution of blowing agent and polymer to produce nuclei of voids and to maintain the nucleation rate high enough to form microfoamed structures in the final product.

In Korean Patent Laid-Open Publication No. 2004-34975, a supercritical gas is introduced into the extruder when the fiber-forming polymer is melted and kneaded in an extruder to prepare a single-phase polymer melt-gas solution having a uniform concentration, and then a sudden rapid pressure. Preparing a microporous discharge by imparting a dropping speed, quenching the microporous discharge with a cooling medium immediately after discharge, and winding it at a winding speed of 10 to 6,000 m / min so that the spinning draft is 2 to 300. A method for producing a microporous fiber is disclosed.

Japanese Patent No. 3,555,986 discloses a gas dissolving step of impregnating a molten thermoplastic resin with an adapter having a first extruder and a mixing portion connected thereto to form a completely compatible state of the thermoplastic resin and the inert gas; (2) A fine process including a cooling process of lowering the temperature of the molten resin while being pressurized by the extruder, a nucleation process of generating a plurality of bubble nuclei by rapid pressure drop, and a foam control process of controlling the bubble diameter. A method for producing a thermoplastic resin foam having a plurality of bubbles uniformly is disclosed.

In Japanese Patent Laid-Open No. 2004-322341, a melting step of melting a molding material containing a crystalline thermoplastic resin, a mixing step of mixing an inert fluid with the molten molding material, and a molding material in a molten state in which the inert fluid is mixed is crystallized. Extrusion foam molding method of a microcell foam is disclosed, including the step of extruding within a range of 0.5 to 5 ℃ high temperature relative to.

In Japanese Patent Laid-Open No. 2004-338396, a melting step of melting a molding material including a thermoplastic resin, a mixing step of mixing an inert fluid with the molten molding material, and a molding material in a molten state in which the inert fluid is mixed is higher than the solidification temperature. Disclosed is an extrusion foam molding method of a microcell foam, including an extrusion process for extruding at a temperature and at an instant of extruding to be in a low foaming state or an external force applying process for applying an external force to the extruded molding material and foaming.

However, the mechanical properties of the final products produced by the above patents are still lower than those of the foam-free.

The present invention is to solve the above problems, the object of the present invention is a microfoam with a low specific gravity, the thickness of the skin layer is thickened, by controlling the size and distribution of the micro-pores of the core layer similar to the non-foamed mechanical It is to provide a micro-foam showing physical properties.

In order to achieve the above object, the present invention includes a skin layer having a porosity of less than 5% and a core layer having a porosity of 5% or more, and provides a microfoam having a thickness of 5 to 50% of the total thickness of the skin layer.

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

The microfoam of the present invention includes a core layer having a thick skin layer and micropores, as compared to a general microfoam. In the present invention, the porosity is calculated by the following formula 1, 'skin layer' is defined as a portion having a porosity of less than 5%, 'core layer' is defined as a portion having a porosity of 5% or more. However, in the present invention, the core layer more preferably has a porosity of 5 to 90% in order to secure excellent mechanical properties.

[Calculation 1]

Porosity (%) = (ρ _N -ρ _F ) / ρ _N × 100

In the above formula, ρ _N represents the density of the foamless body and ρ _F represents the density of the foam.

In the microfoam of the present invention, the thickness of the skin layer is preferably 5 to 50% of the total microfoam thickness, more preferably 10 to 40%. When the thickness of the skin layer is less than 5% of the total microfoam thickness, mechanical properties such as elongation may be lowered, and when the thickness of the skin layer exceeds 50%, it is difficult to obtain a desired specific gravity reduction effect.

The form of the micro-foam of the present invention is not particularly limited, but is preferably in the form of a sheet having a skin layer formed on one or both sides, a L-shaped cross section, or a chassis having a chamber therein. Since the micro-foam can be manufactured to an appropriate thickness according to the use, the thickness of the cross-section of the micro-foam is not particularly limited, but more preferably has a thickness of 0.5 to 5 mm.

In addition, in the micro-foam of the present invention, the skin layer preferably has an average thickness of 50 to 500 ㎛ each. If the thickness of the skin layer is less than 50 ㎛ causes a reduction in mechanical properties, if it exceeds 500 ㎛ it is difficult to obtain the desired specific gravity decrease.

It is preferred that the micro-foam of the present invention have an average porosity of 5 to 80%, more preferably 10 to 70% porosity, and most preferably 15 to 30% porosity. If the total porosity of the micro-foaming body is less than 5% on average, it does not have the characteristics as a micro-foaming, if it exceeds 80% the physical properties of the micro-foaming may be lowered due to excessive pore generation.

In particular, when the total porosity of the total porosity is 15 to 30%, compared to the non-foam prepared under the condition that the impact absorption energy by the rheological drop test measured according to ASTM D 4226 method is equal. It is preferably 70% or more, more preferably 90 to 150%. The higher the shock absorption energy is better, but it is virtually difficult to obtain more than 150% shock absorption energy compared to the foam-free.

The voids formed in the core layer of the micro-foaming body preferably have an average diameter of 0.1 to 50 μm, and preferably have an average diameter of 1 to 30 μm. The smaller the pore size, the better the effect of improving the physical properties of the micro-foam, but it is difficult to form the micro-pore less than 0.1 μm, and when it exceeds 50 μm, the decrease in mechanical properties increases.

The micro-foam of the present invention comprises a thermoplastic resin capable of forming a foam, preferably acrylonitrile-butadiene-styrene (ABS) copolymer, polycarbonate (PC), polyvinyl chloride (PVC), polystyrene (PS) It is preferable to include at least one polymer selected from the group consisting of polymethyl methacrylate (PMMA), polyester, polypropylene, and nylon, acrylonitrile-butadiene-styrene (ABS) copolymer, polycarbonate It is more preferable to include at least one polymer selected from the group consisting of (PC), polyvinyl chloride (PVC), and polystyrene (PS).

The micro-foam of the present invention is preferably 70% or more, more preferably 90 to 150% of the elongation of the non-foam prepared under the same conditions as measured by ASTM D638 method. The higher the elongation of the foam, the better, but it is virtually difficult to obtain an elongation of more than 150% of the foam-free foam, and when the elongation of the foam is less than 70% of the elongation of the foam-free foam, application as a product becomes difficult.

In addition, the micro-foam of the present invention is preferably 70% or more, more preferably 90 to 150% with respect to the tensile strength of the non-foam prepared under the conditions equal to the tensile strength measured according to ASTM D638 method. The higher the tensile strength of the micro-foaming body, the better, but it is virtually difficult to obtain a tensile strength of more than 150% compared to the non-foaming, and less than 70% with respect to the tensile strength of the non-foaming, it is difficult to apply as a product due to the deterioration of physical properties.

The micro-foam of the present invention can be used for the interior and exterior materials for building, or the optical reflecting plate of the display device, if necessary, and is particularly suitable for use as interior and exterior materials for building, in particular soundproofing materials, insulation, building materials, lightweight structural materials, packaging materials, insulation It is suitable for use as interior and exterior building materials for materials, cushioning materials, or dustproof materials.

Method for producing a micro-foam of the present invention is a) mixing a plasticized thermoplastic polymer resin and a blowing agent using an extruder, b) passing the plasticized mixture through a pressure drop section of the extrusion die to form a fine void And c) cooling the molten mixture in which the fine pores are formed while passing through the cooling section of the extrusion die.

At this time, the temperature of the end point of the pressure drop section and the temperature of the start point of the cooling section is preferably to have a temperature difference of 30 to 200 ℃, more preferably to have a temperature difference of 50 to 150 ℃. Do. When the temperature difference is less than 30 ℃, micropores formed in the pressure drop section continues to grow, it is difficult to form a skin layer of sufficient thickness on the foam, when the temperature difference exceeds 200 ℃, due to rapid solidification The process is difficult to proceed.

The pressure drop section and the cooling section may be integrally included in one extrusion die or may be separately included in each block-type extrusion die separated by sections. However, it is preferable to be integrally included in one extrusion die to control micropores and to form a skin layer of the microfoam, and when included separately in the separate extrusion die, the pressure at the end point of the pressure drop section is strongly maintained in the cooling section. It is desirable to fasten.

In addition, the extrusion die may include a heating means for preventing a temperature drop at the end of the pressure drop section. The heating means may be formed inside the pressure drop section of the extrusion die, or may be formed together inside and outside the pressure drop section of the extrusion die.

As the heating means, a normal electric heating element can be used, and other heating means can also be used, and therefore it is not particularly limited in the present invention.

The extrusion die may include cooling means for preventing the temperature rise at the start of the cooling section. The cooling means is also formed inside the cooling section of the extrusion die, as the heating means, it may be formed together inside and outside the cooling section of the extrusion die.

As the cooling means, a cooling device such as a pipeline through which a refrigerant flows can be used, and other cooling means can also be used, and therefore the present invention is not particularly limited.

1 is a cross-sectional view illustrating an example of an extrusion die 10 including a pressure drop section 11, a temperature change section 12, and a cooling section 13. The nozzle 14 is formed in the extrusion direction in the extrusion die 10, and the place where the actual pressure drop is made is the end portion of the nozzle.

The extrusion die includes heating means 15 for maintaining the pressure drop section at a constant temperature, and cooling means 17 for maintaining the temperature of the cooling section. However, the shape of the extrusion die used in the production method of the present invention is not limited only to the case of FIG.

In the production method of the present invention, the temperature of the end point of the pressure drop section can be adjusted to a preferred range depending on the thermoplastic resin used, it is preferably 150 to 250 ℃. If the temperature of the end point of the pressure drop section is less than 150 ℃, it is difficult to form a sufficient micro-pore, if the temperature exceeds 250 ℃ there is a risk of deterioration of the thermoplastic resin and over-foaming.

In addition, the temperature of the start point of the cooling section can also be adjusted to a desired range according to the thermoplastic resin used, it is preferable to maintain at a level slightly higher than the melting point or softening point of the thermoplastic resin, more preferably 40 to 150 ℃ desirable. If the temperature of the start point of the cooling section is less than 40 ℃, the manufacturing process is difficult to proceed due to the rapid solidification, if the temperature exceeds 150 ℃ micropores formed in the pressure drop section continues to grow even in the cooling section. It is difficult to form a skin layer of sufficient thickness.

In particular, the temperature change in the pressure drop section and the cooling section is preferably maintained within ± 5 ℃, more preferably within ± 2 ℃. When the temperature change in the pressure drop section and the cooling section exceeds ± 5 ℃, it is difficult to obtain a uniform extrudate and the mechanical properties are lowered.

The feed rate of the thermoplastic polymer resin in the pressure drop section and the cooling section is not particularly limited within a range capable of securing the normal processability, but is preferably 0.5 to 20 m / min.

 In the method for producing a micro-foam of the present invention may include a temperature change section between the pressure drop section and the cooling section. In the temperature change section, a sudden temperature change occurs, and serves to prevent heat exchange between the pressure drop section and the cooling section. In the temperature change section, it is preferable that the temperature change rate in the advancing direction represented by the following formula 2 is 2 ° C / mm or more, and more preferably 3 to 40 ° C / mm. The higher the temperature change rate is, the better the effect of controlling the micropores by the cooling section is less than 2 ° C / mm.

[Calculation 2]

T _L = (T _h -T _c ) / L

Where T _L is the temperature change rate, T _h is the temperature at the end of the pressure drop section, T _c is the temperature at the start of the cooling section, and L is the length of the temperature change section.

As the length of the temperature change section is narrower, it may cause a sudden temperature change, but the narrower it is, the more advantageous for the manufacturing method of the present invention, but preferably 1 to 150 mm. When the length of the temperature change section exceeds 150 mm, a gentle temperature change occurs between the pressure drop section and the cooling section, which is not preferable for the preparation of the micro-foam.

In this case, the pressure drop section, the temperature change section, and the cooling section are preferably integrally included in one extrusion die. In particular, the extrusion die preferably includes a heating means for preventing the temperature drop at the end of the pressure drop section, it is preferable to include a cooling means for preventing the temperature rise at the start point of the cooling section. At this time, the information about the heating means and the cooling means is the same as the above-described content, the temperature change section may be defined as a section between the heating means and the cooling means.

2 shows an extrusion die 20 in which a plurality of heating means 25 and 26 and cooling means 27 and 28 are added to increase the effect of the heating means and cooling means. Also in this case, it is preferable that the pressure drop section 21, the temperature change section 22, and the cooling section 23 are integrally included in one die. It is also possible to use an extrusion die. The nozzle 24 is formed in the extrusion direction in the extrusion die 20.

The heating means and the cooling means may be added and used in an appropriate number as needed, the shape of the extrusion die used in the production method of the present invention is not limited to the case of FIG.

The thermoplastic polymer resin used in the preparation of the micro-foam of the present invention may be any thermoplastic resin capable of forming a foam, preferably an acrylonitrile-butadiene-styrene (ABS) copolymer or a polycarbonate (PC). , Polyvinyl chloride (PVC), polystyrene (PS), polymethyl methacrylate (PMMA), polyester, polypropylene (PP), and preferably comprises one or more polymers selected from the group consisting of nylon, It is more preferred to include at least one polymer selected from the group consisting of acrylonitrile-butadiene-styrene (ABS) copolymers, polycarbonate (PC), polyvinylchloride (PVC), and polystyrene (PS).

In addition, the blowing agent used in the production method of the present invention preferably uses an inert gas, more preferably using carbon dioxide, nitrogen, or a mixture of these. In addition, the blowing agent is preferably mixed in 3 to 0.1 parts by weight with respect to 97 to 99.9 parts by weight of the thermoplastic resin. When the content of the blowing agent is less than 0.1 parts by weight, sufficient foaming does not occur in the pressure drop section, so that the micropores cannot be formed, and when the content of the blowing agent is more than 3 parts by weight, it is no longer melted in the resin.

The blowing agent is preferably mixed in a supercritical state. When the foaming agent is in the supercritical state, the compatibility with the polymer resin is increased to form uniform pores in the resin, and the pore size can be reduced and the pore density can be increased. The blowing agent may be converted into a supercritical state after using the blowing agent which is already in a supercritical state or after being introduced into the extruder.

For example, for carbon dioxide, the critical pressure is 75.3 kgf / cm ² , the critical temperature is 31.35 ° C., for nitrogen the critical pressure is 34.6 kgf / cm ² , and the critical temperature is -147 ° C. Typically, the conditions for converting the gas into the supercritical state in the extruder are preferably 70 to 400 kgf / cm ² at a pressure of 100 to 400 ° C.

In addition, the conditions for converting the nitrogen into the supercritical state may be adjusted according to the type of blowing agent used, and therefore, the present invention is not limited to a specific range.

Hereinafter, preferred embodiments of the present invention are described. However, the following examples are only preferred embodiments of the present invention, and the present invention is not limited to the following examples.

EXAMPLE

Example 1

As shown in FIG. 3, the extrusion die 34 and the adapter 35 in which the pressure drop section 31, the temperature change section 32, and the cooling section 33 are integrally formed may be twin-screw extruders (G ㆆ ttfert). Extrusiometer 350) (36) was prepared to the extrusion device 30 for producing a micro-foam. At this time, the length of the pressure drop section 31 of the extrusion die was 125 mm, the length of the temperature change section 32 was 27 mm, and the length of the cooling section 33 was 40 mm.

98 parts by weight of a hard polyvinyl chloride (PVC) compound (manufactured by LG Chemical), which is used for interior and exterior materials of windows and buildings, is introduced into the extruder to completely plasticize the PVC, and 2 parts by weight of nitrogen is added to the extruder using a high pressure pump. It was injected into barrel 4 of 3 to prepare a mixture of a single phase, which was foam molded to prepare a microfoam sheet having a thickness of 2 mm and a width of 100 mm.

The extruder conditions were such that the temperature of the barrel 1 was 190 ° C., the barrels 2-4 were 180 ° C., the barrel 5 was 175 ° C., and the adapter was maintained at 135 ° C.

In addition, the pressure drop section, the temperature change section, and the cooling section of the extrusion die are summarized in Table 1 below.

Examples 2 to 3

A micro-foam sheet was prepared in the same manner as in Example 1 except that the barrel conditions of the extruder, the pressure drop section, the temperature change section, and the cooling section of the extruder were changed as shown in Table 1 below.

Example 4

The conditions of the barrel of the extruder and the pressure drop section, the temperature change section, and the cooling section of the extrusion die are changed as shown in Table 1 below, and the remaining conditions except for using a die having a sheet having a thickness of 1 mm are used in Example 1 In the same manner as the prepared microfoam sheet.

Comparative Example 1

Except not using a blowing agent, having a temperature change section and a cooling section as shown in Figure 4, except that the extrusion die 40 using only the nozzle 44 and the heating means 45, 46 in the pressure drop section is used. A foam-free sheet was prepared in the same manner as in Example 1.

Comparative Example 2

Foamed body in the same manner as in Example 1 except for using the extrusion die 40, which has only the nozzle 44 and the heating means 45, 46 in the pressure drop section without having a temperature change section and a cooling section as shown in FIG. Sheets were prepared.

Comparative Example 3

5 includes a pressure drop section 51, a temperature change section 52, and a cooling section 53, the nozzle 54 is formed inside the pressure drop section, the heating means (outside the pressure drop section) 55) is provided, and the foam sheet in the same manner as in Example 1, except that the conditions of Table 1 are applied by using the extrusion die 50 provided with cooling means (57, 58) in the cooling section. Was prepared.

TABLE 1

Temperature (℃) Pressure drop section Temperature change section Cooling section location starting point End point starting point End point starting point End point Example 1 165 165 165 52 52 50 Example 2 175 175 175 45 45 43 Example 3 160 160 160 50 50 50 Example 4 177 177 177 77 77 74 Comparative Example 1 180 180 - - - - Comparative Example 2 180 180 - - - - Comparative Example 3 170 155 145 100 91 75

[Test Example]

The physical properties of the sheets prepared according to Examples 1 to 4 and Comparative Examples 1 to 3 were measured by the following methods, and the results are summarized in Table 2 below.

1. Specific gravity: The specific gravity of the entire sheet was measured according to the ASTM D 792 method.

2. Porosity, pore size, and thickness of skin layer: After the fracture surface was cut out on the sheet, it was measured using a scanning electron microscope (SEM).

FIG. 6 is a fracture scanning electron microscope photograph of the microfoam sheet according to Example 1, and FIG. 7 is a fracture scanning electron microscope photograph of the foam sheet according to Comparative Example 3. FIG.

3. Tensile Strength, and Elongation: Tensile strength and elongation of the sheet were measured according to the ASTM D 638 method.

4. Impact resistance strength: The impact absorption energy was measured by the ASTM D 4226 method using a rheological drop test (RDT) apparatus.

TABLE 2

division Example 1 Example 2 Example 3 Example 4 Comparative Example 1 Comparative Example 2 Comparative Example 3 importance 1.2 1.14 1.2 1.15 1.4 1.0 1.0 Skin layer thickness (㎛) 300 300 200 150 none Less than 50 Less than 50 Average pore size (㎛) 30 20 25 30 none 126 60 % Elongation 136 150 136 112 130 24 42 Tensile Strength (N / mm ² ) 40 43 41 44 44 23.9 36 Shock Absorption Energy (J) 12 13 11 8 15.2 1.2 3.3

As shown in Table 2, the micro-foam produced according to an embodiment of the present invention has a fine pore size, uniform distribution, as shown in Figure 6, the skin layer is thick, the same level as the non-foamed sheet even at low specific gravity On the other hand, the foam sheet of the comparative example which does not form a cooling section or undergoes a gentle cooling treatment has a large pore size and a thin skin layer as shown in FIG.

 Compared with the general microfoam, the microfoam of the present invention has a thicker skin layer, a smaller size of the micropores of the core layer, and a uniform distribution thereof, and thus exhibits similar mechanical properties to those of the conventional nonfoam.

Claims (16)

Including a thermoplastic polymer resin including a skin layer having a porosity of less than 5% and a core layer having a porosity of 5% or more, as defined by Formula 1 below, The thermoplastic polymer resin is acrylonitrile-butadiene-styrene (ABS) copolymer, polycarbonate (PC), polyvinyl chloride (PVC), polystyrene (PS), polymethyl methacrylate (PMMA), polyester, polypropylene (PP), and at least one resin selected from the group consisting of nylon, Microfoam having a thickness of the skin layer of 5 to 50% of the total thickness: [Calculation 1] Porosity (%) = (ρ _N -ρ _F ) / ρ _N × 100 Where ρ _N is the density of foam-free and ρ _F is the density of foam. The microfoam according to claim 1, wherein the microfoam has a sheet having a skin layer formed on one or both surfaces thereof, a L-shaped cross section, or a chassis having a chamber therein. The microfoam according to claim 2, wherein the microfoam has a sheet having a thickness of 0.5 to 5 mm, a cross section, or a chassis having a chamber therein. The micro-foam of claim 1, wherein the skin layer has an average thickness of 50 to 500 μm. The microfoam according to claim 1, wherein the total porosity of the microfoam is 5 to 80%. The non-foaming body of claim 1, wherein the micro-foaming body has a porosity of 15 to 30% and a shock-absorbing energy produced by the rheological drop test measured according to ASTM D 4226. 70% or more of the microfoam. According to claim 6, wherein the micro-foam has a total porosity of 15 to 30%, the non-foaming body prepared under the same conditions as the impact absorption energy by the rheological drop test (Rheometric Drop Test) measured according to the ASTM D 4226 method 90 to 150% of the micro-foam. The micro-foam of claim 1, wherein the core layer has pores having an average diameter of 0.1 to 50 μm. The microfoam according to claim 1, wherein the microfoam has a total porosity of 15 to 30% and an elongation measured according to the ASTM D638 method is 70% or more with respect to the elongation of the nonfoam prepared under the same conditions. The microfoam according to claim 9, wherein the microfoam has a total porosity of 15 to 30% and an elongation of 90% to 150% with respect to the elongation of the nonfoam prepared under the same conditions as measured by ASTM D638. The microfoam according to claim 1, wherein the microfoam has a total porosity of 15 to 30% and is 70% or more with respect to the tensile strength of the non-foam prepared under the same conditions as measured by ASTM D638. The micro-foam of claim 11, wherein the micro-foam has a total porosity of 15 to 30% and 90 to 150% with respect to the tensile strength of the non-foam prepared under the same conditions as measured by ASTM D638. delete The microfoam of claim 1, wherein the microfoam is a building interior and exterior material. The method of claim 1, wherein the micro-foaming body a) mixing the plasticized thermoplastic polymer resin and the blowing agent using an extruder; b) passing the plasticized mixture through a pressure drop zone to form fine pores; And c) passing the molten mixture having the fine pores through the cooling section and cooling the mixture; The temperature of the end point of the pressure drop section and the temperature of the start point of the cooling section has a temperature difference of 30 to 200 ℃, manufactured using an extrusion die (die) including both the pressure drop section and the cooling section Microfoam. The method according to claim 15, wherein the micro-foaming body further comprises a temperature change section between the pressure die section and the cooling section of the extrusion die, and according to the direction of travel in the temperature change section represented by Formula 2 below. Microfoam which is prepared by a manufacturing method having a temperature change rate of 2 to 40 ℃ / mm: [Calculation 2] T _L = (T _h -T _c ) / L Where T _L is the temperature change rate, T _h is the temperature at the end of the pressure drop section, T _c is the temperature at the start of the cooling section, and L is the length of the temperature change section.

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