KR20070022419A - Ethylene vinyl Acetate CopolymerEVA compounds for a footwear sole, Method for producing a sponge by using thereof and a sponge - Google Patents

Ethylene vinyl Acetate CopolymerEVA compounds for a footwear sole, Method for producing a sponge by using thereof and a sponge Download PDF

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KR20070022419A
KR20070022419A KR1020050076605A KR20050076605A KR20070022419A KR 20070022419 A KR20070022419 A KR 20070022419A KR 1020050076605 A KR1020050076605 A KR 1020050076605A KR 20050076605 A KR20050076605 A KR 20050076605A KR 20070022419 A KR20070022419 A KR 20070022419A
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parts
sponge
vinyl acetate
ethylene vinyl
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임희순
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • C08L23/0846Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
    • C08L23/0853Vinylacetate
    • AHUMAN NECESSITIES
    • A43FOOTWEAR
    • A43BCHARACTERISTIC FEATURES OF FOOTWEAR; PARTS OF FOOTWEAR
    • A43B1/00Footwear characterised by the material
    • A43B1/14Footwear characterised by the material made of plastics
    • AHUMAN NECESSITIES
    • A43FOOTWEAR
    • A43BCHARACTERISTIC FEATURES OF FOOTWEAR; PARTS OF FOOTWEAR
    • A43B13/00Soles; Sole-and-heel integral units
    • A43B13/02Soles; Sole-and-heel integral units characterised by the material
    • A43B13/04Plastics, rubber or vulcanised fibre
    • AHUMAN NECESSITIES
    • A43FOOTWEAR
    • A43BCHARACTERISTIC FEATURES OF FOOTWEAR; PARTS OF FOOTWEAR
    • A43B17/00Insoles for insertion, e.g. footbeds or inlays, for attachment to the shoe after the upper has been joined
    • A43B17/003Insoles for insertion, e.g. footbeds or inlays, for attachment to the shoe after the upper has been joined characterised by the material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/02Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of definite length, i.e. discrete articles
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/20Compounding polymers with additives, e.g. colouring
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0014Use of organic additives
    • C08J9/0028Use of organic additives containing nitrogen
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/09Carboxylic acids; Metal salts thereof; Anhydrides thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L97/00Compositions of lignin-containing materials
    • C08L97/02Lignocellulosic material, e.g. wood, straw or bagasse
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/02Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Footwear And Its Accessory, Manufacturing Method And Apparatuses (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Abstract

본 발명은 신발창용 에틸렌 비닐아세테이트 공중합체 조성물에 관한 것으로서, 더욱 상세하게는 코르크 자체의 팽창력과 에틸렌 비닐아세테이트 공중합체 조성물(이하 EVA라 한다)의 발포배율을 응용하여 코르크 분말을 배합과 동시에 첨가하여 된 신발창(안창, 중창 및 밑창)용 발포용 스펀지를 제조하기 위한 에틸렌 비닐아세테이트 공중합체 조성물 및 이를 이용한 스펀지의 제조방법이 제공된다. The present invention relates to an ethylene vinyl acetate copolymer composition for footwear, and more specifically, by applying the expansion coefficient of the cork itself and the expansion ratio of the ethylene vinyl acetate copolymer composition (hereinafter referred to as EVA) by adding the cork powder at the same time with the compounding Provided are an ethylene vinyl acetate copolymer composition for producing a foam for a shoe sole (insole, midsole and sole) and a method for producing a sponge using the same.

코르크, 스펀지, EVA, 가교제, 연화제, 발포제, 신발창 Cork, sponge, EVA, crosslinking agent, softener, foaming agent, sole

Description

신발창용 에틸렌 비닐아세테이트 공중합체 조성물, 이를 이용한 신발창 제조용 스펀지의 제조방법 및 신발창용 스펀지{Ethylene vinyl Acetate Copolymer(EVA) compounds for a footwear sole, Method for producing a sponge by using thereof and a sponge}Ethylene vinyl Acetate Copolymer (EVA) compounds for a footwear sole, Method for producing a sponge by using approximately and a sponge}

도 1은 본 발명의 신발창 제조용 스펀지의 제조방법을 도시한 공정도.1 is a process chart showing a method of manufacturing a shoe sole manufacturing sponge of the present invention.

본 발명은 신발창용 에틸렌 비닐아세테이트 공중합체 조성물에 관한 것으로서, 더욱 상세하게는 코르크 자체의 팽창력과 에틸렌 비닐아세테이트 공중합체 조성물(이하 EVA라 한다)의 발포배율을 응용하여 코르크 분말을 배합과 동시에 첨가하여 된 신발창(안창, 중창 및 밑창)용 발포용 스펀지를 제조하기 위한 에틸렌 비닐아세테이트 공중합체 조성물 및 이를 이용한 스펀지의 제조방법에 관한 것이다. The present invention relates to an ethylene vinyl acetate copolymer composition for footwear, and more specifically, by applying the expansion coefficient of the cork itself and the expansion ratio of the ethylene vinyl acetate copolymer composition (hereinafter referred to as EVA) by adding the cork powder at the same time with the compounding The present invention relates to an ethylene vinyl acetate copolymer composition for producing a foam for a shoe sole (insole, midsole and sole) and a method for producing a sponge using the same.

통상적으로 신발의 창은 일정한 경도, 인장력, 신장력, 인력, 복원력, 충격흡수, 마모, 미끄럼 방지, 성형성 등 각 부품의 특성에 따라 요구되는 물리적 특성 이 매우 중요하다. Typically, the window of the shoe is very important physical properties required according to the characteristics of each part, such as constant hardness, tensile force, elongation, attractive force, restoring force, shock absorption, wear, non-slip, moldability.

종래의 신발창용 스펀지는 대부분 열가소성 합성수지스펀지를 사용하여 만들고 있다. 이것은 합성수지스펀지가 가지고 있는 열가소성의 성질 때문에 우수한 성형성을 가지고 있어 작업성이 매우 용이하기 때문에 대부분 합성수지스펀지를 사용한다. Conventional shoe sole sponges are mostly made using a thermoplastic synthetic resin sponge. Since most synthetic resin sponges have excellent moldability due to the thermoplastic properties of the resin and workability is very easy, most synthetic resin sponges are used.

반면에 내열성이 매우 약하고 압축변형이 나쁘기 때문에 보통 운동화를 착용하고 일주일 정도 경과 되면 안창에 사용된 합성수지스펀지가 얇아지는 것도 함성수지스펀지가 열에 약하고 압축변형이 나쁘기 때문이다. On the other hand, because the heat resistance is very weak and the compression deformation is bad, the synthetic resin sponge used in the insole becomes thinner about a week after wearing sneakers, because the synthetic resin sponge is weak in heat and the compression deformation is bad.

신발의 중창(Midsole) 또한 이와 같은 현상은 마찬가지이다. Midsoles of shoes are the same.

이와 같이 약한 내열성과 압축변형은 부품의 경도에 따라서 차이는 있지만 합성수지스펀지의 최대의 단점이다.Such weak heat resistance and compressive deformation are the biggest disadvantages of the synthetic resin sponge, although there are differences depending on the hardness of the parts.

종래의 합성수지스펀지의 제조방법은 널리 알려져 있으나 간단히 요약하면 EVA수지에다 발포제, 가교제, 조제 등을 배합하여 혼합기에 1차 믹싱 후 로루기에거 2차 믹싱 작업을 한 다음 카렌다에서 두께 2~4mm정도 시트를 만든 다음 냉각 한 후 열프레스에서 압축가열하여 제조하게 된다. 이때 평판 시트의 규격은 금형치수와 발포배율에 따라 다르게 나타난다. Conventional methods of manufacturing synthetic resin sponges are widely known, but briefly summarized, after mixing the EVA resin with a blowing agent, a crosslinking agent, a preparation agent, etc., first mixing in a mixer, and then performing a second mixing operation in a rougegi sheet, and then sheeting about 2 to 4 mm thick in a calendar. After cooling, it is manufactured by compression heating in a heat press after cooling. At this time, the specification of the flat sheet is different depending on the mold size and the expansion ratio.

한편 높은 내열성과 가벼움, 습기조절, 충격흡수, 복원력 등 신발창에서 요구되는 중요한 물리적 특성을 많이 가지고 있는 천연코르크를 분말화하여 합성수지와 혼합하여 제조하거나 또는 코르크 분말에 접착제 처리를 한 다음 압축하여 시트를 만들어 신발창을 만들어 사용하기도 하지만 상기 코르크분말을 사용하여 제조할 경우 매우 고가이고 작업성도 좋지 못한 단점이 있어 특수한 경우에만 일부 국한되어 사용되고 있다. On the other hand, natural cork, which has many important physical properties such as high heat resistance, lightness, moisture control, shock absorption, and resilience, is powdered and manufactured by mixing with synthetic resin or by applying adhesive treatment to cork powder and compressing the sheet. It is also used to make a shoe sole, but when manufactured using the cork powder is very expensive and has a disadvantage of poor workability has been limited to some special cases are used.

또한, 열가소성 합성수지스펀지와 천연코르크의 장점을 살리기 위하여 합성수지스펀지와 코르크분말을 이용하여 제조된 시트를 일정한 규격으로 만들어 접착가공을 한 다음 성형금형에 넣고 압축하여 열냉각 방식을 이용하여 신발창을 제조한다. 그러나 이러한 방법은 작업공정(접착, 재단 등)의 증가로 인하여 원가 상승 및 난이도가 높은 형상은 성형이 어려운 문제가 있다. In addition, in order to take advantage of the thermoplastic synthetic resin sponge and natural cork, the sheet manufactured using the synthetic resin sponge and the cork powder is made to a certain standard, and then subjected to adhesive processing, and then put into a molding mold and compressed to manufacture a shoe sole using a thermal cooling method. . However, this method is difficult to mold the shape of high cost and difficulty due to the increase of the work process (gluing, cutting, etc.).

따라서, 본 발명은 상기와 같은 종래의 문제점을 해결하기 위한 것으로서, 천연코르크의 우수한 물리적 특성과 합성수지스펀지의 물리적 특성을 잘 조정하여 다량의 코르크를 배합하여 신발창의 특성에 맞는 에틸렌 비닐아세테이트 공중합체 조성물, 이를 이용한 신발창 제조용 스펀지의 제조방법 및 신발창 제조용 스펀지를 제공하는 것을 기술적 과제로 한다. Accordingly, the present invention is to solve the conventional problems as described above, ethylene vinyl acetate copolymer composition suitable for the characteristics of the sole by mixing a large amount of cork by adjusting the physical properties of the natural cork excellent physical properties and synthetic resin sponge well It is a technical problem to provide a method for manufacturing a shoe sole manufacturing sponge using the same and a shoe sole manufacturing sponge.

상기와 같은 기술적 과제를 해결한 본 발명은 에틸렌 비닐아세테이트 공중합체 100중량부, 코르크미분말 5~50중량부, 연화제 0.5~2.5중량부, 가교제 0.5~1.5중량부 및 발포제 2.0~8.0중량부로 이루어진 것을 특징으로 하는 신발창용 에틸렌 비닐아세테이트 공중합체 조성물을 제공한다. The present invention that solved the above technical problem is composed of 100 parts by weight of ethylene vinyl acetate copolymer, 5 to 50 parts by weight of cork fine powder, 0.5 to 2.5 parts by weight of softener, 0.5 to 1.5 parts by weight of crosslinking agent and 2.0 to 8.0 parts by weight of blowing agent. An ethylene vinyl acetate copolymer composition for footwear is provided.

또한, 본 발명은 에틸렌 비닐아세테이트 공중합체 100중량부, 코르크미분말 5~50중량부, 연화제 0.5~2.5중량부, 가교제 0.5~1.5중량부를 혼합기에 넣고 온도 80~90℃에서 12~14분간 혼합한 후 발포제 2.0~8.0중량부를 투입하여 1~3분간 혼합하는 1차 혼합공정, 상기 1차 혼합된 배합물을 2차혼합기인 믹싱롤에서 표면온도 70~80℃에서 13~17분 동안 혼합하는 2차 혼합공정, 상기 2차 혼합된 배합물을 상온에서 2시간 이상 냉각 및 숙성시키는 공정, 상기 배합물을 믹싱롤에서 표면온도 70~80℃에서 13~17분 동안 재혼합하는 3차 혼합공정, 상기 혼합된 배합물을 3본 카렌다에서 가로 500m/m 세로 1000m/m 두께 2~3m/m이 되도록 절단하여 상온에서 2시간 이상 냉각 및 숙성시키는 공정, 상기 냉각된 배합물을 금형규격에 따라 평량한 다음 금형에 투입한 후 152~158℃ 온도, 160㎏f/㎠의 압력으로 42분동안 가류 및 발포하는 프레스발포공정 및 상기 프레스발포공정에서 제조된 스펀지를 냉각하는 공정으로 이루어진 것을 특징으로 하는 신발창용 스펀지 제조방법을 제공한다. In the present invention, 100 parts by weight of ethylene vinyl acetate copolymer, 5 to 50 parts by weight of cork fine powder, 0.5 to 2.5 parts by weight of a softener, and 0.5 to 1.5 parts by weight of a crosslinking agent were put into a mixer, and mixed at a temperature of 80 to 90 ° C. for 12 to 14 minutes. After the first mixing step of mixing for 1 to 3 minutes by adding 2.0 to 8.0 parts by weight of the blowing agent, the second mixing the primary blended mixture for 13 to 17 minutes at a surface temperature 70 ~ 80 ℃ in a mixing roll which is a secondary mixer Mixing step, the step of cooling and aging the second blended blend at room temperature for 2 hours or more, the third blending step of remixing the blend in a mixing roll for 13-17 minutes at a surface temperature of 70 ~ 80 ℃, the mixed The compound is cut in three calenders to have a width of 500 m / m and a length of 1000 m / m and a thickness of 2 to 3 m / m, followed by cooling and aging at room temperature for at least 2 hours. The cooled compound is weighed according to mold specifications and then put into a mold. 152 ~ 158 ℃ temperature, 160kgf / ㎠ pressure In the press foaming step of vulcanizing and foaming for 42 minutes and provides a sponge manufacturing method for a shoe sole, characterized in that consisting of a step of cooling the sponge produced in the press foaming step.

또한, 본 발명은 상기한 기재의 방법으로 제조되는 신발창 제조용 스펀지를 제공한다. The present invention also provides a shoe sole manufacturing sponge manufactured by the method described above.

이하, 본 발명을 첨부도면을 참조하여 보다 상세히 설명하면 다음과 같다. Hereinafter, the present invention will be described in more detail with reference to the accompanying drawings.

첨부도면 도 1은 본 발명의 신발창 제조용 스펀지의 제조공정을 나타낸 공정도이다. Accompanying drawings Figure 1 is a process diagram showing the manufacturing process of the shoe sole manufacturing sponge of the present invention.

본 발명에서 제안하고자 하는 것은 천연코르크가 지니고 있는 장점을 최대한 살리면서 열가소성 스펀지의 우수한 작업성과 장점을 동시에 가질 수 있는 신발창 제조용 스펀지 및 상기 스펀지를 제조하기 위한 에틸렌 비닐아세테이트 공중합체 조성물을 제안하고자 하는 것이다. It is to be proposed in the present invention to propose a shoe sole manufacturing sponge and an ethylene vinyl acetate copolymer composition for preparing the sponge that can simultaneously have the excellent workability and advantages of the thermoplastic sponge while maximizing the advantages of natural cork. .

즉, 에틸렌 비닐아세테이트 공중합체(이하 EVA라 한다)와 가교제, 연화제, 발포제, 코르크분말을 혼합기에서 1차 혼합을 한 다음 2차 혼합기 믹싱롤에서 재혼합을 한 후 냉각하여 열프레스기에 압축하여 발포시킨다. 이때 코르크 입자가 연결이 되면 오픈셀이 되어 불량이 발생되므로 많은 주의를 요한다. 이와 같이 제조된 스펀지는 EVA와 코르크를 동시에 함유하고 있어 합성수지스펀지와 코르크의 물리적특성을 동시에 지니게 된다. That is, the ethylene vinyl acetate copolymer (hereinafter referred to as EVA), the crosslinking agent, the softener, the foaming agent, and the cork powder are first mixed in a mixer, then remixed in a secondary mixer mixing roll, cooled, compressed into a hot press, and foamed. Let's do it. At this time, when the cork particles are connected, it becomes an open cell, which requires a lot of attention. The sponge thus prepared contains EVA and cork at the same time, thereby simultaneously possessing physical properties of the synthetic resin sponge and cork.

이에 대한 상세한 조성비 및 제조방법을 첨부도면 도 1을 참조하여 설명한다. Detailed composition ratio and manufacturing method thereof will be described with reference to FIG. 1.

본 발명에 따르는 에틸렌 비닐아세테이트 공중합체 조성물은 에틸렌 비닐아세테이트 공중합체, 코르크미분말, 연화제, 가교제 및 발포제로 이루어진다.The ethylene vinyl acetate copolymer composition according to the present invention consists of ethylene vinyl acetate copolymer, cork fine powder, softener, crosslinking agent and blowing agent.

여기서 상기 에틸렌 비닐아세테이트 공중합체는 통상의 사용되는 것을 이용하며, 상기 코르크미분말은 통상의 천연코르크를 이용하여 평균입경 0.1~3.0㎜이 되도록 분말화하여 사용하며, 에틸렌비닐아세테이트 공중합체 100중량부에 대해 5~50중량부를 첨가하는 것이 바람직하다. 만일 그 첨가량이 5중량부 미만일 경우 코르크가 가지는 물리적 성질을 기대할 수 없는 문제가 있고, 50중량부를 초과하여 될 경우에는 제조원가의 상승 및 발포성 저하와 작업성이 현저히 떨어지는 문제가 있다. 또한, 사용되는 코르크분말의 평균입경이 0.1㎜미만인 경우에는 코르크 입자가 미세하여 코르크 형상이 잘 나타나지 아니하고, 3.0㎜이상일 경우는 코르크입자 와 입자가 서로 연결이 되어 오픈셀이 되어 불량이 발생하게 되는 문제가 있다. Here, the ethylene vinyl acetate copolymer is used in the conventional one, and the fine cork powder is used to powder to an average particle diameter of 0.1 ~ 3.0㎜ using a normal natural cork, to 100 parts by weight of ethylene vinyl acetate copolymer It is preferable to add 5-50 weight part with respect to. If the added amount is less than 5 parts by weight, there is a problem that the physical properties of the cork can not be expected, if it exceeds 50 parts by weight, there is a problem that the rise in manufacturing cost, the foamability and the workability is significantly reduced. In addition, when the average particle diameter of the cork powder to be used is less than 0.1 mm, the cork particles are fine and the cork shape does not appear well. there is a problem.

본 발명에 사용되는 상기 연화제로는 스테아린산을 사용하며 그 첨가량은 0.5~2.5인 것이 바람직하다. 만일 그 첨가량이 0.5중량부 미만일 경우에는 유연성의 감소 및 혼합작업이 나쁜 문제가 있고, 2.5중량부를 초과할 경우에는 표면에 침출하거나 물성이 저하되는 문제가 발생하게 된다. 상기 스테아린산 외에 본 발명을 저해하지 않는 범위에서 통상 사용되는 다른 연화제를 사용할 수 있다. Stearic acid is used as the softener used in the present invention, and the amount thereof is preferably 0.5 to 2.5. If the added amount is less than 0.5 parts by weight, there is a problem of reduced flexibility and poor mixing operation, and if it exceeds 2.5 parts by weight, the problem of leaching on the surface or deteriorated physical properties. In addition to the stearic acid described above, other emollients commonly used within the scope of not inhibiting the present invention can be used.

본 발명에 사용되는 상기 가교제는 DCP(Dicumyl Peroxide)를 사용하며 그 첨가량은 0.5~1.5인 것이 바람직하다. 만일 그 첨가량이 0.5중량부 미만일 경우에는 미가류현상이 발생하거나 가류시간이 길어져 생산성이 떨어지는 문제가 있고, 1.5중량부를 초과할 경우에는 과가류가 일어나 발포율이 저하되고 기포불량발생으로 인하여 물성이 저하되는 문제가 발생하게 된다. 상기 DCP외에 본 발명을 저해하지 않는 범위에서 통상 사용되는 다른 가교제를 사용할 수 있다. The crosslinking agent used in the present invention uses DCP (Dicumyl Peroxide), and the amount thereof is preferably 0.5 to 1.5. If the added amount is less than 0.5 parts by weight, there is a problem of uncured phenomena or a long vulcanization time, resulting in a decrease in productivity. When it is more than 1.5 parts by weight, excess vulcanization occurs, resulting in a decrease in foaming rate and poor foaming. This deterioration problem occurs. In addition to the above DCP, other crosslinking agents usually used in a range that does not inhibit the present invention can be used.

본 발명에 사용되는 상기 발포제는 아조디카본아마이드(AD, Azodicarbonamide)를 사용하며, 그 첨가량은 2.0~8.0인 것이 바람직하다. 만일 그 첨가량이 2.0중량부 미만일 경우에는 저발포로 인하여 경도가 높고 비중이 높음으로 스펀지의 기능이 상실되는 문제가 있고, 8.0중량부를 초과할 경우에는 발포개스의 과다발생으로 스펀지의 불량이 발생하는 문제가 있다. 상기 아조디카본아마이드 외에 본 발명을 저해하지 않는 범위에서 통상사용되는 발포제를 사용할 수 있다. The blowing agent used in the present invention uses azodicarbonamide (AD, Azodicarbonamide), the amount is preferably 2.0 ~ 8.0. If the amount is less than 2.0 parts by weight, there is a problem in that the function of the sponge is lost due to high hardness and high specific gravity due to low foaming. If it exceeds 8.0 parts by weight, the sponge may be defective due to excessive foam gas. there is a problem. In addition to the azodicarbonamide, a blowing agent usually used in a range that does not inhibit the present invention can be used.

본 발명에 있어서, 상기한 조성물 외에 본 발명을 저해하지 않는 범위에서 신발창(안창, 중창 및 밑창)의 사용용도에 따라 물성을 조절하기 위하여 각종 블렌 드용 수지, 고무 또는 기타의 충전제를 더욱 첨가할 수 있다. In the present invention, various blending resins, rubbers or other fillers may be further added to control the physical properties according to the use of the sole (insole, midsole, and sole) in the range that does not inhibit the present invention in addition to the above-described composition. have.

이상과 같이 구성되는 본 발명의 에틸렌 비닐아세테이트 공중합체 조성물을 이용하여 신발창을 제조하기 위해 사용되는 스펀지를 제조하는 공정을 설명하면 다음과 같다. Referring to the process for producing a sponge used to manufacture a shoe sole using the ethylene vinyl acetate copolymer composition of the present invention configured as described above are as follows.

먼저 에틸렌 비닐아세테이트 공중합체 100중량부, 코르크미분말 5~50중량부, 연화제 0.5~2.5중량부, 가교제0.5~1.5중량부를 혼합기에 넣고 온도 80~90℃에서 12~14분간 혼합한 후 발포제 2.0~8.0중량부를 투입하여 1~3분간 1차 혼합기에서 혼합하고(S100, S110), 상기 1차 혼합된 배합물을 2차혼합기인 믹싱롤에서 표면온도 70~80℃에서 13~17분 동안 재혼합하여 상온에서 2시간 이상 냉각 및 숙성시키고(S120, S130), 상기 숙성된 배합물을 믹싱롤에서 표면온도 70~80℃에서 13~17분 동안 재혼합한 후 3본 카렌다에서 가로 500m/m 세로 1000m/m 두께 2~3m/m이 되도록 절단하여 상온에서 2시간 이상 냉각 및 숙성시키고(S140, S150, S160), 상기 냉각된 배합물을 금형규격에 따라 평량(평량예: 금형규격이 620 × 1140 × 19m/m일경우 투입중량은 11,500g이 된다)한 다음 금형에 투입한 후 152~158℃ 온도, 160㎏f/㎠의 압력으로 42분동안 가류 및 발포하는 프레스발포 후 상온에서 자연냉각하여 스펀지를 제조하게 된다(S170, S180, S190, S200).First, 100 parts by weight of ethylene vinyl acetate copolymer, 5 to 50 parts by weight of cork fine powder, 0.5 to 2.5 parts by weight of softener, and 0.5 to 1.5 parts by weight of crosslinking agent are added to a mixer, and mixed at a temperature of 80 to 90 ° C. for 12 to 14 minutes, followed by foaming agent 2.0 to 8.0 parts by weight was added and mixed in the primary mixer for 1 to 3 minutes (S100, S110), and the mixture was mixed firstly in a mixing roll which is a secondary mixer at a surface temperature of 70 to 80 ℃ for 13 to 17 minutes at room temperature After cooling and ripening for at least 2 hours at (S120, S130), the aged compound was remixed for 13 to 17 minutes at a surface temperature of 70 to 80 ℃ in a mixing roll, and then 500 m / m length and 1000 m / m thickness in three calenders. Cut to 2 ~ 3m / m and cooled and aged at room temperature for 2 hours or more (S140, S150, S160), and the basis weight according to the mold specification (Balance weight: 620 × 1140 × 19m / m Weight is 11,500g), and then put into mold, and then the temperature is 152 ~ 158 ℃, 16 After pressing foaming and foaming for 42 minutes at a pressure of 0 kgf / cm 2, the sponge is naturally cooled at room temperature to prepare a sponge (S170, S180, S190, and S200).

상기 배합물의 투입중량은 금형규격에 따라 다르게 평량되며 그 투입중량 계산방법은 아래의 수학식 1 과 같다. The input weight of the compound is basis weight differently according to the mold specification and the input weight calculation method is as shown in Equation 1 below.

수학식Equation 1 One

투입중량=(금형의 가로×세로×높이)/압축 배합물 비중Input weight = (width × length × height of mold) / specific gravity of compression compound

이하, 본 발명을 바람직한 실시예를 들어 보다 상세히 설명하기로 한다. 그러나 본 발명이 하기 실시예에 의해 한정되는 것은 아니다. Hereinafter, the present invention will be described in more detail with reference to preferred embodiments. However, the present invention is not limited by the following examples.

[실시예 1]Example 1

EVA공중합체 100중량부에 코르크미분말 40중량부, 연화제로 스테아린산 1.3중량부, 가교제로 DCP 0.9중량부 및 발포제로 AD 6.1중량부를 용량 75리터의 리다기에서 1차 혼합하고, 상기 1차 혼합물을 믹싱롤에서 2차 혼합하여 상온에서 냉각 숙성시칸 후 다시 믹싱롤에서 3차 혼합을 한다. 상기 3차혼합물을 3본 카렌다에서 규격 500×1000×2m/m인 시트를 제조하고 자연냉각한 후 규격 620×1140×19m/m인 금형에 중량 11,500g을 투입하고 열프레스에서 발포하여 스펀지를 제조한 후, 가로 150m/m 세로 200m/m 두께 10m/m의 크기로 시편을 제조하여 각종 물성을 시험하였으며 그 결과는 표 1에 기재하였다. 100 parts by weight of EVA copolymer, 40 parts by weight of fine cork powder, 1.3 parts by weight of stearic acid as a softener, 0.9 parts by weight of DCP as a crosslinking agent and 6.1 parts by weight of AD as a blowing agent were mixed first in a 75 liter capacity Lida group, and the primary mixture was mixed. Secondary mixing in the mixing roll, and then cooled and aged at room temperature, the third mixture is mixed again in the mixing roll. The third mixture is prepared in three calenders, and the sheet is 500 × 1000 × 2m / m in size. Naturally cooled, 11,500 g of the weight is added to a mold of 620 × 1140 × 19m / m and foamed in a hot press. After the preparation, specimens were prepared in a size of 150 m / m horizontal 200 m / m thickness 10 m / m and tested for various physical properties. The results are shown in Table 1.

[비교예 1]Comparative Example 1

EVA 공붕합체 100중량부에 연화제로 스테아린산 1.3중량부, 가교제로 DCP 0.9중량부 및 발포제로 AD 6.1중량부를 혼합하여 실시예1과 같은 방법으로 스펀지를 제조한 후 시편을 제조하여 각종 물성을 시험하였으며 그 결과는 표 1에 나타내었다. 1.3 parts by weight of stearic acid as a softener, 0.9 parts by weight of DCP as a crosslinking agent and 6.1 parts by weight of AD as a blowing agent were mixed with 100 parts by weight of the EVA co-condensate to prepare a sponge in the same manner as in Example 1, and then specimens were prepared and tested for various physical properties. The results are shown in Table 1.

〈표 1〉<Table 1>

물성항목  Property item 기준치 Reference value 실시예 Example 비교예 Comparative example 인 장  Seal 10.0이상 10.0 or more 14kg/㎠ 14kg / ㎠ 15kg/㎠ 15kg / ㎠ 인 렬  Fragment 6.0이상 6.0 and above 8kg/㎝ 8kg / cm 9kg/㎝ 9 kg / cm 신장율  Elongation 80이상 80 or more 110% 110% 180% 180% 수 축  Shrink 1.0이하 1.0 or less 0.3% 0.3% 0.8% 0.8% 경 도  Hardness C TYPE C TYPE 48° 48 ° 40° 40 ° 비 중  importance 0.26이하 0.26 or less 0.23 0.23 0.19 0.19 축변형율  Axial strain 65%이하 65% or less 55% 55% 65% 65%

상기 결과에서 보는 바와 같이 코르크 입자의 배합으로 합성수지 스펀지에 비하여 압축변형율 및 수축경도의 물성이 현저히 증가함을 알 수 있다. As shown in the results, it can be seen that the physical properties of the compressive strain and the shrinkage hardness are significantly increased compared to the synthetic resin sponge by the cork particles.

이상 설명한 바와 같이 제조된 스펀지를 사용하여 각종 신발창을 제조할 경우 합성수지가 가지고 있는 물성과 코르크가 가지고 있는 물성을 동시에 가지게 됨으로써 종래의 합성수지 또는 코르크만으로 된 스펀지에 비해 경제성이 우수하고 합성수지와 코르크의 상호보완작용을 하게 되어 각종 물성이 우수한 신발창을 제조할 수 있어 종래의 합성수지만으로 제조된 신발창에 비해 경도, 영구압축변형률이 우수하게 된다. When manufacturing various shoe soles using the sponges prepared as described above, the synthetic resins and cork have the same properties as those of synthetic resins or cork-only sponges. Complementary effect makes it possible to manufacture a shoe sole excellent in various physical properties, it is excellent in hardness, permanent compression strain compared to a shoe sole made of conventional synthetic resin.

이상 설명한 바와 같이 본 발명에 따르는 신발창용 조성물은 에틸렌 비닐아세테이트 공중합체에 천연코르크 분말을 첨가하여 각종 블렌드물과 혼합한 후, 이 혼합물을 이용하여 신발창용 스펀지를 제조할 경우 합성수지와 코르크의 물리적특성이 상호 보완작용을 하여 압축변형, 내열성 등 신발창 제조시 요구되는 각종 물리적 특성이 향상되는 효과가 있다. As described above, the sole composition according to the present invention is mixed with various blends by adding natural cork powder to ethylene vinyl acetate copolymer, and then, when manufacturing the sole sponge using the mixture, physical properties of the synthetic resin and cork This complementary action has the effect of improving the various physical properties required for the production of the shoe sole, such as compression deformation, heat resistance.

또한, 코르크만으로 제조할 경우 문제가 되는 작업공정성 및 원가상승의 문제도 합성수지와의 혼합조성에 의해 개선되는 효과가 있다. In addition, the problem of work processability and cost increase, which is a problem when manufactured only with cork, is also improved by mixing composition with synthetic resin.

Claims (8)

에틸렌 비닐아세테이트 공중합체 100중량부, 코르크미분말 5~50중량부, 연화제 0.5~2.5중량부, 가교제 0.5~1.5중량부 및 발포제 2.0~8.0중량부를 혼합하여 된 것을 특징으로 하는 신발창용 에틸렌 비닐아세테이트 공중합체 조성물.100 parts by weight of ethylene vinyl acetate copolymer, 5 to 50 parts by weight of cork fine powder, 0.5 to 2.5 parts by weight of softener, 0.5 to 1.5 parts by weight of crosslinking agent and 2.0 to 8.0 parts by weight of foaming agent. Coalescing composition. 제 1 항에 있어서, 상기 코르크미분말의 평균입경은 0.1~3.0㎜인 것을 특징으로 하는 신발창용 에틸렌 비닐아세테이트 공중합체 조성물.The sole ethylene vinyl acetate copolymer composition according to claim 1, wherein the cork fine powder has an average particle diameter of 0.1 to 3.0 mm. 제 1 항에 있어서, 상기 연화제는 스테아린산인 것을 특징으로 하는 신발창용 에틸렌 비닐아세테이트 공중합체 조성물.The sole ethylene vinyl acetate copolymer composition according to claim 1, wherein the softener is stearic acid. 제 1 항에 있어서, 상기 가교제는 DCP인 것을 특징으로 하는 신발창용 에틸렌 비닐아세테이트 공중합체 조성물.The sole ethylene vinyl acetate copolymer composition according to claim 1, wherein the crosslinking agent is DCP. 제 1 항에 있어서, 상기 발포제는 아조디카본아마이드인 것을 특징으로 하는 신발창용 에틸렌 비닐아세테이트 공중합체 조성물.The method of claim 1 wherein the blowing agent is ethylene vinyl acetate copolymer composition, characterized in that the azodicarbonamide. 에틸렌 비닐아세테이트 공중합체 100중량부, 코르크미분말 5~50중량부, 연화제 0.5~2.5중량부, 가교제 0.5~1.5중량부를 혼합기에 넣고 온도 80~90℃에서 12~14분간 혼합한 후 발포제 2.0~8.0중량부를 투입하여 1~3분간 혼합하는 1차 혼합공정,100 parts by weight of ethylene vinyl acetate copolymer, 5 to 50 parts by weight of cork fine powder, 0.5 to 2.5 parts by weight of softener, 0.5 to 1.5 parts by weight of crosslinking agent, were mixed in a mixer at a temperature of 80 to 90 ° C. for 12 to 14 minutes, and then foaming agent 2.0 to 8.0. First mixing process by mixing 1 to 3 minutes by weight, 상기 1차 혼합된 배합물을 2차혼합기인 믹싱롤에서 표면온도 70~80℃에서 13~17분 동안 혼합하는 2차 혼합공정,A secondary mixing step of mixing the first blended blend for 13 to 17 minutes at a surface temperature of 70 ~ 80 ℃ in a mixing roll which is a secondary mixer, 상기 2차 혼합된 배합물을 상온에서 2시간 이상 냉각 및 숙성시키는 공정,Cooling and aging the secondary mixed formulation at room temperature for at least 2 hours, 상기 배합물을 믹싱롤에서 표면온도 70~80℃에서 13~17분 동안 재혼합하는 3차 혼합공정,Tertiary mixing process of re-mixing the compound for 13 to 17 minutes at a surface temperature of 70 ~ 80 ℃ in a mixing roll, 상기 혼합된 배합물을 3본 카렌다에서 가로 500mm 세로 1000mm 두께 2~3mm이 되도록 절단하여 상온에서 2시간 이상 냉각 및 숙성시키는 공정,The mixed compound is cut in three calenders to have a thickness of 500mm length 1000mm thickness 2-3mm, cooling and aging at room temperature for 2 hours or more, 상기 냉각된 배합물을 금형규격에 따라 평량한 다음 금형에 투입한 후 152~158℃ 온도, 160㎏f/㎠의 압력으로 42분동안 가류 및 발포하는 프레스발포공정 및 Press cooled step of weighing the cooled compound according to the mold specification and then injecting into the mold for vulcanization and foaming for 42 minutes at a temperature of 152 ~ 158 ℃, 160kgf / ㎠ and 상기 프레스발포공정에서 제조된 스펀지를 냉각하는 공정으로 이루어진 것을 특징으로 하는 신발창용 스펀지의 제조방법.Method for producing a shoe sole sponge, characterized in that consisting of a step of cooling the sponge produced in the press foaming process. 제 6 항에 있어서, 상기 코르크미분말의 평균입경은 0.1~3.0㎜인 것을 특징으로 하는 신발창용 스펀지의 제조방법.The method of claim 6, wherein the average particle diameter of the fine cork powder is 0.1 ~ 3.0mm. 청구항 제 6항 내지 제7항 기재의 방법으로 제조되는 것을 특징으로 하는 신발창용 스펀지.A sponge for a shoe sole, which is produced by the method of claim 6.
KR1020050076605A 2005-08-22 2005-08-22 Ethylene vinyl Acetate CopolymerEVA compounds for a footwear sole, Method for producing a sponge by using thereof and a sponge KR100695401B1 (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100967137B1 (en) * 2008-10-20 2010-07-05 임희순 the ethylene vynil acetate copolymer composition for insole and the manufacturing method for insole sponge utilizing the same
KR101067512B1 (en) * 2009-01-16 2011-09-27 전명자 EVA form composition, method for manufacturing thereof and moulding used it
KR101293154B1 (en) * 2010-07-29 2013-08-12 에코메이드(주) Method for producing a sponge by using Ethylene vinyl Acetate and sulphur powder

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ES2379185B1 (en) * 2010-07-29 2012-11-02 Gregorio Sánchez García Soto PROCEDURE FOR THE MANUFACTURE OF FOOTWEAR FLOORS WITH CORK ASPECT.

Family Cites Families (6)

* Cited by examiner, † Cited by third party
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US4042543A (en) 1976-02-13 1977-08-16 Strickman Robert L Material for stoppers
JPH0815441B2 (en) * 1993-06-26 1996-02-21 ヤマト株式会社 Sandals that fit well on the foot and manufacturing method
KR970010857B1 (en) * 1993-10-15 1997-07-01 한국신발피혁연구소 Composition for binder
KR950023343A (en) * 1994-01-05 1995-08-18 장규용 Manufacturing method of shoe sole using cork
KR20000003134A (en) * 1998-06-26 2000-01-15 치아-챵 첸 Mid sol manufacturing method using cork imitating material and product thereof
KR20020089604A (en) * 2001-05-23 2002-11-30 이명재 an insole of shoes and its manufacturing method

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100967137B1 (en) * 2008-10-20 2010-07-05 임희순 the ethylene vynil acetate copolymer composition for insole and the manufacturing method for insole sponge utilizing the same
KR101067512B1 (en) * 2009-01-16 2011-09-27 전명자 EVA form composition, method for manufacturing thereof and moulding used it
KR101293154B1 (en) * 2010-07-29 2013-08-12 에코메이드(주) Method for producing a sponge by using Ethylene vinyl Acetate and sulphur powder

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