KR20130104550A - Primer composition for difficulty adhesion shoe material without halogen - Google Patents

Primer composition for difficulty adhesion shoe material without halogen Download PDF

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KR20130104550A
KR20130104550A KR1020120026144A KR20120026144A KR20130104550A KR 20130104550 A KR20130104550 A KR 20130104550A KR 1020120026144 A KR1020120026144 A KR 1020120026144A KR 20120026144 A KR20120026144 A KR 20120026144A KR 20130104550 A KR20130104550 A KR 20130104550A
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weight
primer composition
shoe material
resin
adhesive
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KR101357270B1 (en
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천제환
정부영
천정미
오상택
김태균
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한국신발피혁연구원
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04Polyurethanes
    • C09D175/14Polyurethanes having carbon-to-carbon unsaturated bonds
    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/34Silicon-containing compounds
    • C08K3/346Clay
    • 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
    • C08K5/01Hydrocarbons
    • 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
    • C08K5/05Alcohols; Metal alcoholates
    • 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
    • C08K5/07Aldehydes; Ketones
    • 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
    • C08K5/10Esters; Ether-esters
    • C08K5/101Esters; Ether-esters of monocarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/04Homopolymers or copolymers of esters
    • C08L33/14Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur, or oxygen atoms in addition to the carboxy oxygen
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/20Diluents or solvents
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/60Additives non-macromolecular
    • C09D7/61Additives non-macromolecular inorganic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/60Additives non-macromolecular
    • C09D7/63Additives non-macromolecular organic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/65Additives macromolecular

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Dispersion Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

PURPOSE: A non-halogen type primer composition is provided to improve wettability and cohesive force without using harmful aromatic solvent and halogenic resin, and the adhesive strength of an inadhesive shoe material such as biodegradable ethylene vinyl acetate form, etc. CONSTITUTION: A primer composition comprises 2-6 weight% of polyurethane acrylate resin, 1.0-2.5 weight% of thermoplastic polyurethane resin, 0.5-1.5 weight% of nanocomposite, 0.5-1.5 weight% of tackifier, and 88.5-96 weight% of solvent. Polyurethane prepolymer including hydroxyl group is manufactured using 35-45 mole% of polycaprolactone having hydroxyl group in the end and 50 mole% of diisocyanate. The polyurethane acrylate resin is manufactured by synthesizing the polyurethane prepolymer with 5-15 mole% of hydroxyethyl methacrylate as a chain lengthener.

Description

비할로겐 타입 난접착 신발 소재용 프라이머 조성물{PRIMER COMPOSITION FOR DIFFICULTY ADHESION SHOE MATERIAL WITHOUT HALOGEN}Primer composition for non-halogen type non-adhesive shoes material {PRIMER COMPOSITION FOR DIFFICULTY ADHESION SHOE MATERIAL WITHOUT HALOGEN}

본 발명은 비할로겐 타입 난접착 신발 소재용 프라이머 조성물에 관한 것으로, 더욱 상세하게는 난접착 신발 소재인 생분해성 에텔렌비닐아세테이트계 폼 등에 대한 접착력이 우수하면서도 유해성 방향족 용제와 할로겐 함유 수지를 사용하지 않아 친환경적인 비할로겐 타입 난접착 신발 소재용 프라이머 조성물에 관한 것이다.
The present invention relates to a primer composition for non-halogen-type hard-adhesive shoe materials, and more particularly, does not use harmful aromatic solvents and halogen-containing resins while having excellent adhesion to biodegradable ethylene vinyl acetate-based foams which are hard-adhesive shoe materials. It relates to a primer composition for environmentally friendly non-halogen type non-adhesive shoe material.

현재 신발산업에서는 신발용 부품으로 에텔렌비닐아세테이트계 폼 소재가 미드솔 및 인솔 용도로 다수 사용되고 있으며, 상기 에틸렌비닐아세테이트 폼 소재가 비극성이기 때문에 접착이 어려워 통상적으로 프라이머 처리에 의한 표면처리를 한 후 UV를 조사하고 프라이머 및 접착제 순으로 도포하여 신발용 부품들을 접착하고 있지만 저장 안정성 및 접착력을 신뢰할 수 없는 문제점이 있었다.
Currently, in the shoe industry, ethylene vinyl acetate foam materials are used for midsoles and insoles as shoe parts, and since the ethylene vinyl acetate foam materials are non-polar, they are difficult to bond, and thus, after surface treatment by primer treatment, UV is usually applied. Was investigated and applied in the order of primer and adhesive in order to bond the shoe parts, but there was a problem that the storage stability and adhesion strength is not reliable.

따라서, 상기 에텔렌비닐아세테이트계 폼 소재와 같은 난접착 신발 소재의 접착력을 향상시키기 위하여 극성 용제를 사용하여 프라이머를 제조하였으나 이는 작업자들의 건강을 저해하고 작업시 불쾌감을 유발하며 환경보호의 측면에서도 좋지 않은 영향을 미치고 있는 등의 문제점을 가지고 있어 가능한 자극적인 용제의 사용을 최대한 줄이고 프라이머의 접착력 등 접착물성을 개선시키기 위한 연구개발들이 활발히 진행되었다.
Therefore, in order to improve the adhesion of the hard-adhesive shoe material, such as the ethylene vinyl acetate foam material, a primer was prepared using a polar solvent, which impairs the health of workers and causes discomfort during work and is also good in terms of environmental protection. The research and development has been actively carried out to reduce the use of irritating solvents as possible and to improve adhesive properties such as primer adhesion.

이에, 본 출원인은 특허문헌 1인 대한민국 공개특허공보 제10-2010-0078473호와 같은 프라이머 조성물을 선출원하였으며, 상기 선출원된 프라이머 조성물은 열가소성 폴리우레탄 수지에 염화폴리올레핀 수지, 접착증진제, 실란 커플링제, 저독성 용제를 사용하여 프라이머를 제조함으로써, 난접착성 신발소재에 대한 접착력을 향상시키면서도 작업자가 휘발성 유독 유기용제로부터 받는 위생성의 피해를 감소시켜 쾌적한 작업 환경을 유지시킬 수 있도록 하였다.
Accordingly, the present applicant has filed a primer composition such as Korean Patent Application Publication No. 10-2010-0078473, which is Patent Document 1, wherein the primer composition is applied to a thermoplastic polyurethane resin, a polyolefin resin, an adhesion promoter, a silane coupling agent, By preparing a primer using a low toxicity solvent, while improving the adhesion to the hard-adhesive shoe material while reducing the damage to the hygiene from workers volatile organic solvents to maintain a comfortable working environment.

하지만, 최근 각종 산업에서 사용하는 다양한 종류의 부품 소재들은 기능성과 환경친화성을 동시에 고려하여 제품 사용 후 생태계에서 자연적으로 분해되는 생분해성 소재를 사용하여 신발 부품을 제조하고자 하는 노력이 진행되고 있다.However, in recent years, various kinds of component materials used in various industries are considering efforts to manufacture shoe parts using biodegradable materials that are naturally decomposed in an ecosystem after product use in consideration of functionality and environmental friendliness.

따라서, 자연적으로 분해가 되지 않는 상기 에틸렌비닐아세테이트 폼에 자연적으로 분해될 수 있는 폴리락트산(polylactic acid) 등을 30~40%정도 사용하여 생분해성 신발용 폼을 제조하고 있다.
Therefore, the biodegradable shoe foam is manufactured using about 30 to 40% of polylactic acid, which can be naturally decomposed, to the ethylene vinyl acetate foam that is not naturally decomposed.

하지만, 본 출원인은 대한민국 공개특허공보 제10-2010-0078473호와 같은 프라이머 조성물은, 에텔렌비닐아세테이트계 폼 소재와 같은 난접착 신발 소재에 접착력을 향상시킬 수는 있으나, 폴리락트산 등의 생분해성 물질이 포함된 난접착 신발 소재의 접착력을 향상시키는데는 한계가 있었다.However, the present applicant is a primer composition such as the Republic of Korea Patent Publication No. 10-2010-0078473, although it is possible to improve the adhesion to the non-adhesive shoe material, such as ethylene vinyl acetate foam material, biodegradability such as polylactic acid There has been a limit to improving the adhesion of the hard-adhesive shoe material containing the material.

그 이유는, 폴리락트산 등의 생분해성 물질이 포함된 난접착 신발 소재에 단순히 방향족계 저독성 용제를 사용하면 프라이머의 주성분인 폴리머의 용해가 쉽지 않고 생분해성 에틸렌비닐아세테이트 폼에 젖음성이 저하되는 문제점이 있었을 뿐만 아니라 치수안정성이 저하되고 부품 표면이 훼손되어 상품가치가 떨어지는 문제점이 있었다.
The reason for this is that simply using an aromatic low toxicity solvent in a hard-adhesive shoe material containing biodegradable substances such as polylactic acid is not easy to dissolve the polymer, which is the main component of the primer, and the wettability of the biodegradable ethylene vinyl acetate foam is reduced. Not only that, there was a problem that the dimensional stability was lowered and the surface of the part was damaged, resulting in a drop in product value.

즉, 종래에는 생분해성 에틸렌비닐아세테이트 폼 등과 같은 난접착 신발 소재의 접착력을 향상시킬 수 있으면서도 유해성 방향족 용제와 화합물 및 장기적으로 작업자의 건강 및 환경을 해칠 수 있는 할로겐 함유 수지를 사용하지 않는 프라이머 조성물이 부재한 실정이며, 이에 대한 개발이 지속적으로 요구되고 있다.
That is, in the related art, a primer composition which can improve adhesion of hard-adhesive shoe materials such as biodegradable ethylene vinyl acetate foam, but does not use harmful aromatic solvents and compounds and halogen-containing resins that can harm the health and environment of workers in the long term, The situation is absent, the development of this is constantly required.

: 대한민국 공개특허공보 제10-2010-0078473호 "접착보강용 프라이머 조성물": Republic of Korea Patent Publication No. 10-2010-0078473 "Adhesive reinforcing primer composition"

본 발명은 상기와 같은 문제점을 해결하기 위한 것으로, 폴리우레탄 아크릴레이트 수지, 열가소성 폴리우레탄 수지, 나노복합재, 점착부여제 및 3종 이상의 용제로 이루어진 프라이머 조성물을 제공함으로써, 유해성 방향족 용제와 할로겐 함유 수지를 사용하지 않으면서도 그 젖음성 및 응집력을 향상시켜 생분해성 에틸렌비닐아세테이트 폼 등과 같은 난접착 신발 소재의 접착력을 향상시킨 비할로겐 타입 난접착 신발 소재용 프라이머 조성물을 제공함을 과제로 한다.
The present invention is to solve the above problems, by providing a primer composition consisting of a polyurethane acrylate resin, a thermoplastic polyurethane resin, a nanocomposite, a tackifier and three or more solvents, a hazardous aromatic solvent and a halogen-containing resin It is an object of the present invention to provide a primer composition for a non-halogen type non-adhesive shoe material that improves the wettability and cohesive force without improving the adhesion of the non-adhesive shoe material such as biodegradable ethylene vinyl acetate foam.

또한, 상기 프라이머 조성물에 용제를 사용함에 있어, 페놀, 벤젠, 톨루엔, 자일렌 등의 유해성 방향족 용제를 사용하지 않아 친환경적일 뿐만 아니라 생분해성 에틸렌비닐아세테이트 폼 등과 같은 난접착 신발 소재와 접착제의 상호작용을 고려한 분자설계로부터 조성물의 종류와 조성비를 선정하고, 또한 방향족 탄화수소계를 제외한 용제와 생분해성 에틸렌비닐아세테이트 폼 부품과의 상용성을 개선시킨 비할로겐 타입 난접착 신발 소재용 프라이머 조성물을 제공함을 다른 과제로 한다.
In addition, in using the solvent in the primer composition, it does not use harmful aromatic solvents such as phenol, benzene, toluene, and xylene, which is not only environmentally friendly, but also the interaction between adhesive materials such as biodegradable ethylene vinyl acetate foam and adhesives. To provide a primer composition for the non-halogen type, non-adhesive shoe material that improves the compatibility of the solvent and the biodegradable ethylene vinyl acetate foam parts except the aromatic hydrocarbon type from the molecular design in consideration of It is a task.

본 발명은 난접착 신발 소재용 프라이머 조성물에 있어서, 폴리우레탄 아크릴레이트 수지 2~6 중량%, 열가소성 폴리우레탄 수지 1.0~2.5 중량%, 나노복합재 0.5~1.5 중량%, 점착 부여제 0.5~1.5 중량% 및 용제 88.5~96 중량%로 이루어진 것을 특징으로 하는 비할로겐 타입 난접착 신발 소재용 프라이머 조성물을 과제의 해결 수단으로 한다.
The present invention is a primer composition for hard-adhesive shoe material, 2 to 6% by weight of polyurethane acrylate resin, 1.0 to 2.5% by weight of thermoplastic polyurethane resin, 0.5 to 1.5% by weight of nanocomposite, 0.5 to 1.5% by weight of tackifier And the primer composition for non-halogen type hard-adhesive shoe material which consists of 88.5 to 96 weight% of solvents as a solution to a subject.

이때, 폴리우레탄 아크릴레이트 수지는, 말단에 수산기를 가지고 있는 폴리카프로락톤 35~45 몰%에 디이소시아네이트 50 몰%를 사용하여 말단에 수산기를 포함하는 폴리우레탄 프리폴리머를 제조하고, 사슬연장제로 하이드록시에틸 메타크릴레이트를 5~15 몰% 사용하여 합성한 폴리우레탄 아크릴레이트 화합물을 사용하는 것이 바람직하다.
In this case, the polyurethane acrylate resin is a polyurethane prepolymer containing a hydroxyl group at the end by using 50 mole% of diisocyanate to 35 to 45 mol% of polycaprolactone having a hydroxyl group at the end, and hydroxy as a chain extender It is preferable to use the polyurethane acrylate compound synthesize | combined using 5-15 mol% of ethyl methacrylate.

아울러, 상기 나노복합재는,PEGMA/(Na-MMT)-co-MMA/MA 나노복합재로써, 폴리(에틸렌 글리콜) 메틸 에테르 메타크릴레이트(PEGMA, Poly(ethylene glycol) methyl ether methacrylate)를 소듐 몬모릴로나이트(Na-MMT, Na-montmorillonite)의 층간에 삽입한 후, 메타크릴산메틸(MMA, Methyl Methacrylate) 및 아크릴산메틸(MA, Methyl Acrylate) 단량체와의 공중합시킨 화합물이다.
In addition, the nanocomposite, PEGMA / (Na-MMT) -co-MMA / MA nanocomposite, poly (ethylene glycol) methyl ether methacrylate (PEGMA, Poly (ethylene glycol) methyl ether methacrylate) to sodium montmorillonite ( The compound is inserted between the layers of Na-MMT and Na-montmorillonite, and then copolymerized with methyl methacrylate (MMA) and methyl acrylate (MA) monomers.

또한, 상기 용제는, 노말 헥산, 에틸아세테이트, 메틸에틸케톤, 아세톤, 이소프로필알콜, 에탄올, 메탄올, 싸이클로헥산, 메틸싸이클로헥산으로 이루어진 군에서 3종 이상 병용하여 사용하는 것이 바람직하다.
In addition, the solvent is preferably used in combination of three or more of the group consisting of normal hexane, ethyl acetate, methyl ethyl ketone, acetone, isopropyl alcohol, ethanol, methanol, cyclohexane, and methyl cyclohexane.

본 발명은 폴리우레탄 아크릴레이트 수지, 열가소성 폴리우레탄 수지, 나노복합재, 점착부여제 및 3종 이상의 용제로 이루어진 프라이머 조성물을 제공함으로써, 유해성 방향족 용제 및 할로겐 함유 수지를 사용하지 않아 친환경적이며, 생분해성 에틸렌비닐아세테이트 폼 등과 같은 소재의 접착력을 향상시킬 뿐만 아니라 상기 소재가 사용되는 분야인 신발 산업, 가구 산업 분야 등 다양한 산업분야에 널리 적용할 수 있는 장점이 있다.
The present invention provides a primer composition consisting of a polyurethane acrylate resin, a thermoplastic polyurethane resin, a nanocomposite, a tackifier, and three or more solvents, thereby avoiding the use of hazardous aromatic solvents and halogen-containing resins, thereby being environmentally friendly and biodegradable ethylene. In addition to improving the adhesive strength of the material, such as vinyl acetate foam, there is an advantage that can be widely applied to a variety of industries, such as the shoe industry, furniture industry, the field in which the material is used.

상기의 효과를 달성하기 위한 본 발명은 비할로겐 타입 난접착 신발 소재용 프라이머 조성물에 관한 것으로서, 본 발명의 기술적 구성을 이해하는데 필요한 부분만이 설명되며 그 이외 부분의 설명은 본 발명의 요지를 흩트리지 않도록 생략될 것이라는 것을 유의하여야 한다.
The present invention for achieving the above effect relates to a primer composition for non-halogen type non-adhesive shoe material, only the parts necessary for understanding the technical configuration of the present invention is described, the description of other parts scatter the gist of the present invention. Note that it will be omitted so as not to fall short.

이하, 본 발명에 따른 비할로겐 타입 난접착 신발 소재용 프라이머 조성물을 상세히 설명하면 다음과 같다.
Hereinafter, the primer composition for a non-halogen type hard-adhesive shoe material according to the present invention will be described in detail.

본 발명은 난접착 신발 소재용 프라이머 조성물에 있어서, The present invention is a primer composition for non-adhesive shoe material,

폴리우레탄 아크릴레이트 수지 2~6 중량%, 열가소성 폴리우레탄 수지 1.0~2.5 중량%, 나노복합재 0.5~1.5 중량%, 점착 부여제 0.5~1.5 중량% 및 용제 88.5~96 중량%로 이루어진 것을 특징으로 한다.
2 to 6% by weight of polyurethane acrylate resin, 1.0 to 2.5% by weight of thermoplastic polyurethane resin, 0.5 to 1.5% by weight of nanocomposite, 0.5 to 1.5% by weight of tackifier and 88.5 to 96% by weight of solvent. .

본 발명에 사용된 폴리우레탄 아크릴레이트 수지는 피착재의 표면젖음성 및 응집력을 향상시키기 위한 역할을 하며, 2~6 중량%를 사용하는 것이 바람직하다. 폴리우레탄 아크릴레이트 수지의 함량이 2 중량% 미만이 될 경우에는 기재에 대한 부착성, 젖음성 등의 화학적 성능이 저하되어 접착력이 감소하게 될 우려가 있으며, 6 중량%를 초과하면 프라이머의 가격 상승의 원인이 되며, 수지 용액의 점도가 증가하고 작업성 및 용제에 대한 용해도가 저하될 우려가 있다.
Polyurethane acrylate resin used in the present invention serves to improve the surface wettability and cohesion of the adherend, it is preferable to use 2 to 6% by weight. If the content of the polyurethane acrylate resin is less than 2% by weight, chemical performance such as adhesion to the substrate, wettability, etc. may be degraded, thereby reducing the adhesion. There is a concern that the viscosity of the resin solution increases and the workability and solubility in the solvent decrease.

한편, 상기 폴리우레탄 아크릴레이트 수지는 말단에 수산기를 가지고 있는 폴리카프로락톤 35~45 몰%에 디이소시아네이트를 50 몰%를 사용하여 말단에 수산기를 포함하는 폴리우레탄 프리폴리머를 제조하고, 사슬연장제로 하이드록시에틸 메타크릴레이트를 5~15 몰% 사용하여 합성한 폴리우레탄 아크릴레이트 화합물을 사용한다.
On the other hand, the polyurethane acrylate resin is a polyurethane prepolymer containing a hydroxyl group at the end by using 50 mol% of diisocyanate in 35 ~ 45 mol% of polycaprolactone having a hydroxyl group at the end, and a hydro-extension agent The polyurethane acrylate compound synthesize | combined using 5-15 mol% of oxyethyl methacrylate is used.

이때, 상기 폴리카프로락톤의 사용량이 35 몰% 미만일 경우, 폴리우레탄 아크릴레이트의 물성이 너무 하드(hard)하여 초기 고정성이 저하될 우려가 있으며, 45 몰%를 초과할 경우, 응집력이 떨어져 프라이머의 접착력을 저하시킬 우려가 있다.At this time, when the amount of the polycaprolactone is less than 35 mol%, there is a risk that the physical properties of the polyurethane acrylate is too hard (hard), the initial fixability is lowered, if it exceeds 45 mol%, cohesive force is lowered primer There is a risk of reducing the adhesive strength of the.

아울러, 디이소시아네이트의 사용량이 50 몰%을 벗어날 경우, 폴리우레탄이 충분히 합성되지 않을 우려가 있다.In addition, when the usage-amount of diisocyanate exceeds 50 mol%, there exists a possibility that a polyurethane may not fully synthesize | combine.

한편, 사슬연장제의 사용량이 5 몰% 미만일 경우, 소프트 세그멘트(soft segment)의 함량이 증가하여 유연성은 증가하나 기계적 물성이 취약해 질수 있고 15 몰%를 초과할 경우, 하드 세그멘트(hard segment)의 함량이 증가하여 딱딱해질 우려가 있다.
On the other hand, when the amount of the chain extender is less than 5 mol%, the soft segment content increases to increase the flexibility, but the mechanical properties may be weak, and when the content exceeds 15 mol%, the hard segment There is a fear that the content of is increased and becomes hard.

본 발명에서 사용된 열가소성 폴리우레탄 수지는 접착강도, 내노화성, 응집력이 우수하고 높은 강도를 발현하는 수지로서, 취급하기에 용이하고 다른 수지와의 혼합이 용이한데 이를 1.0~2.5 중량% 범위 내에서 사용하는 것이 바람직하다. 열가소성 폴리우레탄 수지의 함량이 1.0 중량% 미만이 될 경우에는 응집력이 저하되어 접착력이 감소하게 될 우려가 있고, 열가소성 폴리우레탄 수지의 함량이 2.5 중량%를 초과하면 프라이머의 점도가 증가하여 작업성이 떨어져 접착불량의 원인이 될 수 있으며, 프라이머의 사용량이 많아져 경제성이 저하된다.
The thermoplastic polyurethane resin used in the present invention is excellent in adhesive strength, aging resistance, cohesion and high strength, and is easy to handle and easy to mix with other resins, which is within the range of 1.0 to 2.5% by weight. It is preferable to use. If the content of the thermoplastic polyurethane resin is less than 1.0% by weight, the cohesive force may be reduced to reduce the adhesive strength. If the content of the thermoplastic polyurethane resin is more than 2.5% by weight, the viscosity of the primer may be increased to improve workability. This may cause poor adhesion, and the amount of primer used increases, resulting in lower economic efficiency.

본 발명에서 사용된 나노복합재는 프라이머의 응집력 및 젖음성을 향상하기 위해서 사용하며, 그 사용량은 0.5~1.5 중량% 범위내에서 사용하는 것이 바람직하다. 나노복합재 함량이 0.5 중량% 미만일 때는 첨가 효과가 떨어져 프라이머의 응집력이 떨어지며 1.5 중량%를 초과 사용하였을 때는 나노복합재에 포함되어 있는 나노 무기물에 의해 프라이머의 저장 안정성이 떨어질 우려가 있다.The nanocomposite used in the present invention is used to improve the cohesion and wettability of the primer, and the amount thereof is preferably used in the range of 0.5 to 1.5% by weight. When the content of the nanocomposite is less than 0.5% by weight, the addition effect is reduced, so that the cohesive strength of the primer is lowered. When the content of the nanocomposite is more than 1.5% by weight, the storage stability of the primer may be reduced by the nano-inorganic material contained in the nanocomposite.

한편, 상기 나노복합재는 폴리(에틸렌 글리콜) 메틸 에테르 메타크릴레이트(PEGMA, Poly(ethylene glycol) methyl ether methacrylate)를 소듐 몬모릴로나이트(Na-MMT, Na-montmorillonite)에 삽입한 후, 메타크릴산메틸(MMA, Methyl Methacrylate) 및 아크릴산메틸(MA, Methyl Acrylate) 단량체와의 공중합을 행하여 합성된 PEGMA/(Na-MMT)-co-MMA/MA 나노복합재를 사용하며, 이의 합성방법은 후술하기로 한다.
On the other hand, the nanocomposite is a poly (ethylene glycol) methyl ether methacrylate (PEGMA, Poly (ethylene glycol) methyl ether methacrylate) is inserted into sodium montmorillonite (Na-MMT, Na-montmorillonite) and then methyl methacrylate ( PEGMA / (Na-MMT) -co-MMA / MA nanocomposites synthesized by copolymerization with MMA, Methyl Methacrylate) and Methyl Acrylate (MA) monomers are used.

본 발명에서 사용되는 점착부여제 사용량은 0.5~1.5 중량%를 사용하는 것이 바람직하며, 점착부여제 함량이 0.5 중량% 미만일 경우에는 초기 점착력이 감소하게 될 우려가 있고, 점착부여제 함량이 1.5 중량%를 초과할 경우에는 프라이머 조성에 저분자량이 많아 프라이머의 응집력이 감소하고 특히 점착력이 높아 프라이머의 물성 저하가 우려된다.The amount of the tackifier used in the present invention is preferably 0.5 to 1.5% by weight. When the content of the tackifier is less than 0.5% by weight, the initial adhesive strength may decrease, and the content of the tackifier is 1.5% by weight. When it exceeds%, there are many low molecular weights in the primer composition, so that the cohesive force of the primer decreases, and in particular, the adhesive force is high, so that the physical properties of the primer may be deteriorated.

상기 점착부여제는 석유수지계, 변성 석유수지, 알킬페놀수지, 열가소성 테르펜변성 페놀수지, 로진 및 로진에스테르수지, 쿠마론인덴수지 중에서 1종 또는 그 이상을 선택하여 사용하는 것이 바람직하다.
The tackifier is preferably used by selecting one or more of petroleum resin, modified petroleum resin, alkylphenol resin, thermoplastic terpene modified phenol resin, rosin and rosin ester resin, and coumarone indene resin.

본 발명에 사용된 용제의 함량은 88.5~96 중량%인 것이 바람직하며, 프라이머 조성물의 고형분이 6~10 중량%가 되도록 점도를 조절하여 사용하는 것이 바람직하다. 특히 톨루엔을 사용하지 않기 때문에 프라이머의 용해도가 현저히 떨어지므로 용제를 필히 3종 이상 사용하여야 한다.
The content of the solvent used in the present invention is preferably 88.5 to 96% by weight, it is preferable to adjust the viscosity so that the solid content of the primer composition is 6 to 10% by weight. In particular, since toluene is not used, solubility of the primer is remarkably decreased, so three or more solvents must be used.

본 발명에 사용 가능한 용제는 노말 헥산, 에틸아세테이트, 메틸에틸케톤, 아세톤, 이소프로필알콜, 에탄올, 메탄올, 싸이클로헥산, 메틸싸이클로헥산으로 이루어진 군에서 3종 이상 병용하여 사용하는 것이 바람직하다.
Solvents usable in the present invention are preferably used in combination of three or more from the group consisting of normal hexane, ethyl acetate, methyl ethyl ketone, acetone, isopropyl alcohol, ethanol, methanol, cyclohexane, and methyl cyclohexane.

한편, 상기와 같은 본 발명의 난접착 신발 소재용 프라이머 조성물은 사용시에 이소시아네이트계 경화제를 혼합시켜 사용하여야 한다.
On the other hand, the primer composition for the non-adhesive shoe material of the present invention as described above should be used by mixing isocyanate-based curing agent at the time of use.

본 발명에서 사용 가능한 경화제는 통상적인 경화제로서 이소시아네이트를 상기 프라이머 조성물 100 중량부에 대하여 5~10 중량부 사용하는 것이 바람직하다.It is preferable to use 5-10 weight part of isocyanate with respect to 100 weight part of said primer compositions as a conventional hardening | curing agent which can be used by this invention.

상기에서 경화제의 혼합량이 5 중량부 미만이 될 경우에는 이소시아네이트 혼합량의 부족으로 인해 열가소성 폴리우레탄계 탄성체용 프라이머 조성물이 제대로 경화되지 않을 우려가 있고, 경화제의 혼합량이 10 중량부를 초과할 경우에는 경화속도가 빨라 작업시간이 짧아짐에 따라 불량률이 발생할 우려가 있다. When the mixing amount of the curing agent is less than 5 parts by weight, the primer composition for the thermoplastic polyurethane-based elastomer may not be cured properly due to the lack of the isocyanate mixing amount, and when the mixing amount of the curing agent exceeds 10 parts by weight, the curing rate is increased. As the working time gets shorter as soon as possible, there is a risk of defective rate.

본 발명에서 사용 가능한 이소시아네이트는 통상적인 용제형 경화제로서 NCO 함량이 6~20% 범위의 것을 사용할 수 있다.
Isocyanate usable in the present invention can be used as a conventional solvent type curing agent having an NCO content of 6 to 20% range.

이하, 본 발명의 실시 예를 들면서 상세히 설명하는 바, 본 발명이 다음의 실시예에 의해서만 반드시 한정되는 것은 아니다.
Hereinafter, the present invention will be described in detail with reference to Examples. However, the present invention is not necessarily limited to the following Examples.

1. 폴리우레탄 아크릴레이트 수지의 제조1. Preparation of polyurethane acrylate resin

환류 냉각기와 교반기, 온도계 및 질소주입장치를 설치한 500ml 반응기에메틸에틸케톤, 폴리카프로락톤(Aldrich, Mw=2000) 40 몰%에 대하여, 메틸렌 비스 (p-시클로헥실 이소시아네이트)(H12MDI) 50 몰%를 투입한 다음 70℃에서 3시간을 100 rpm 의 교반속도로 교반하여 폴리우레탄 프리폴리머를 제조하였다. 다음으로 하이드록시에틸 메타크릴레이트 10 몰%를 투입한 뒤 40℃에서 3시간을 80 rpm의 교반속도로 교반하여 반응시킨 후 용제를 휘발시켜 폴리우레탄 아크릴레이트 수지를 제조하였다.
Methylene bis (p-cyclohexyl isocyanate) (H 12 MDI) with respect to 40 mol% of methyl ethyl ketone and polycaprolactone (Aldrich, Mw = 2000) in a 500 ml reactor equipped with a reflux condenser, a stirrer, a thermometer, and a nitrogen injection device. 50 mol% was added, followed by stirring at 70 ° C. for 3 hours at a stirring speed of 100 rpm to prepare a polyurethane prepolymer. Next, 10 mol% of hydroxyethyl methacrylate was added thereto, followed by stirring at 40 ° C. for 3 hours at a stirring speed of 80 rpm to evaporate the solvent to prepare a polyurethane acrylate resin.

2. 나노복합재의 제조2. Preparation of Nanocomposites

혼합용매를 포함하는 환류 냉각기와 교반기, 온도계 및 질소주입장치를 설치한 250ml 반응기에 진공 건조된 소듐 몬모릴로나이트(Na-MMT)(Southern Clay) 70 중량%, 폴리(에틸렌 글리콜) 메틸 에테르 메타크릴레이트(PEGMA) 30 중량%를 가하여 교반기로 상온에서 24시간 교반하고 원심분리한 것을 혼합용매로 반복하여 세척하고 이것을 진공건조기에서 25℃에서 48시간 동안 건조하여 층간 삽입된 PEGMA/Na-MMT를 제조한 후,70% by weight of vacuum-dried sodium montmorillonite (Na-MMT) (Southern Clay), poly (ethylene glycol) methyl ether methacrylate in a 250 ml reactor equipped with a reflux cooler containing a mixed solvent, a stirrer, a thermometer, and a nitrogen injector. PEGMA) 30% by weight was added and stirred at room temperature with a stirrer for 24 hours, and centrifuged and washed repeatedly with a mixed solvent, which was dried at 25 ° C. for 48 hours in a vacuum dryer to prepare an intercalated PEGMA / Na-MMT. ,

환류 냉각기와 교반기, 온도계 및 질소주입장치를 설치한 1L 4구 반응기에 용매로서 에틸아세테이트를 넣고 PEGMA 또는 상기 PEGMA/Na-MMT를 5 중량%를 가하여 상온에서 3시간 동안 잘 교반하여 분산시킨 후, 혼합 아크릴레이트 단량체 100 중량%에 사슬연장제로 메칼탑 1.5 중량%, 개시제로 아조비스이소부티로나이트릴 0.5 중량%를 가하고 70℃에서 15시간 동안 라디칼 중합을 행하여 PEGMA/(Na-MMT)-co-MMA/MA를 제조하였다.
Ethyl acetate as a solvent was added to a 1 L four-necked reactor equipped with a reflux condenser, a stirrer, a thermometer, and a nitrogen injector. 5 wt% of PEGMA or PEGMA / Na-MMT was added thereto, followed by dispersion for 3 hours at room temperature. To 100% by weight of the mixed acrylate monomer, 1.5% by weight of the mecartop was added as a chain extender and 0.5% by weight of azobisisobutyronitrile as the initiator, followed by radical polymerization at 70 ° C. for 15 hours to give PEGMA / (Na-MMT) -co -MMA / MA was prepared.

3. 난접착 신발 소재용 프라이머 조성물의 제조
3. Preparation of primer composition for non-adhesive shoe material

(실시예 1)(Example 1)

온도조절과 속도조절이 가능한 혼합용기에 폴리우레탄 아크릴레이트 수지 2 중량%, 열가소성 폴리우레탄 수지(pearstic 45-50/18, MERQINSA) 2.5 중량%, 나노복합재 1 중량%에 점착부여제(SU-120, 코오롱유화) 1 중량%를 첨가한 후, 용제로써 메틸에틸케톤 50 중량%, 노말헥산 24.5 중량%, 사이클로헥산 19 중량%를 투입하여 50℃의 온도에서 8시간 교반하여 용해시킨 혼합액의 총고형분이 6.5 중량%인 프라이머 조성물을 제조하였다.
Tackifier (SU-120) in 2% by weight of polyurethane acrylate resin, 2.5% by weight of thermoplastic polyurethane resin (pearstic 45-50 / 18, MERQINSA) and 1% by weight of nanocomposite in a mixing vessel with temperature and speed control 1% by weight of Kolon Emulsifier), 50% by weight of methyl ethyl ketone, 24.5% by weight of normal hexane, and 19% by weight of cyclohexane were added and stirred at a temperature of 50 ° C. for 8 hours to dissolve the total solids. This 6.5 wt% primer composition was prepared.

(실시예 2)(Example 2)

온도조절과 속도조절이 가능한 혼합용기에 폴리우레탄 아크릴레이트 수지 5 중량%, 열가소성 폴리우레탄 수지(pearstic 45-50/18, MERQINSA) 2 중량%, 나노복합재 1.5 중량%에 점착부여제(SU-120, 코오롱유화) 0.5 중량%를 첨가한 후 용제로써 메틸에틸케톤 50 중량%, 노말헥산 27 중량%, 사이클로헥산 15 중량%를 투입하여 50℃의 온도에서 8시간 교반하여 용해시킨 혼합액의 총고형분이 8 중량%인 프라이머 조성물을 제조하였다.Tackifier (SU-120) in 5% by weight of polyurethane acrylate resin, 2% by weight of thermoplastic polyurethane resin (pearstic 45-50 / 18, MERQINSA), and 1.5% by weight of nanocomposite in a mixing vessel with temperature and speed control , Kolon Emulsifier) 0.5% by weight of methyl ethyl ketone, 27% by weight of normal hexane and 15% by weight of cyclohexane were added as a solvent, and the total solid content of the mixed solution was dissolved by stirring at a temperature of 50 ° C for 8 hours. A primer composition of 8% by weight was prepared.

(실시예 3)(Example 3)

온도조절과 속도조절이 가능한 혼합용기에 폴리우레탄 아크릴레이트 수지 3 중량%, 열가소성 폴리우레탄 수지(pearstic 45-50/18, MERQINSA) 2.5 중량%, 나노복합재 1.5 중량%에 점착부여제(SU-120, 코오롱유화) 0.5 중량%를 첨가한 후 용제로써 메틸에틸케톤 50 중량%, 노말헥산 27 중량%, 사이클로헥산 15.5 중량%를 투입하여 50℃의 온도에서 8시간 교반하여 용해시킨 혼합액의 총고형분이 7.5 중량%인 프라이머 조성물을 제조하였다.
Tackifier (SU-120) in 3% by weight of polyurethane acrylate resin, 2.5% by weight of thermoplastic polyurethane resin (pearstic 45-50 / 18, MERQINSA) and 1.5% by weight of nanocomposite in a mixing vessel with temperature and speed control , Kolon Emulsifier) 0.5% by weight of methyl ethyl ketone, 27% by weight of normal hexane and 15.5% by weight of cyclohexane were added as a solvent, and the total solid content of the mixed solution was dissolved by stirring at a temperature of 50 ° C for 8 hours. A 7.5 wt% primer composition was prepared.

(실시예 4)(Example 4)

온도조절과 속도조절이 가능한 혼합용기에 폴리우레탄 아크릴레이트 수지 3 중량%, 열가소성 폴리우레탄 수지(pearstic 45-50/18, MERQINSA) 1 중량%, 나노복합재 1.5 중량%에 점착부여제(SU-120, 코오롱유화) 1.5 중량%를 첨가한 후 용제로써 메틸에틸케톤 50 중량%, 노말헥산 26 중량%, 사이클로헥산 17 중량%를 투입하여 50℃의 온도에서 8시간 교반하여 용해시킨 혼합액의 총고형분이 7 중량%인 프라이머 조성물을 제조하였다.
3% by weight of polyurethane acrylate resin, 1% by weight of thermoplastic polyurethane resin (pearstic 45-50 / 18, MERQINSA), 1.5% by weight of nanocomposite in mixed container with temperature control and speed control (SU-120 , Kolon Emulsification) 1.5% by weight of methyl ethyl ketone, 26% by weight of normal hexane and 17% by weight of cyclohexane were added as a solvent, and the total solid content of the mixed solution was dissolved by stirring at a temperature of 50 ° C for 8 hours. A 7 wt% primer composition was prepared.

(비교예 1)(Comparative Example 1)

온도조절과 속도조절이 가능한 혼합용기에 개질된 염화폴리올레핀 수지 2 중량%, 열가소성 폴리우레탄 수지(pearstic 45-50/18, MERQINSA) 2.5 중량%, 나노복합재 1 중량%에 점착부여제(SU-120, 코오롱유화) 1 중량%를 첨가한 후 용제로써 메틸에틸케톤 50 중량%, 노말헥산 24.5 중량%, 사이클로헥산 19 중량%를 투입하여 50℃의 온도에서 8시간 교반하여 용해시킨 혼합액의 총고형분이 6.5 중량%인 프라이머 조성물을 제조하였다.Tackifier (SU-120) in 2% by weight of chlorinated polyolefin resin, 2.5% by weight of thermoplastic polyurethane resin (pearstic 45-50 / 18, MERQINSA), 1% by weight of nanocomposite material , Kolon Emulsifier) 1% by weight of methyl ethyl ketone, 24.5% by weight of normal hexane and 19% by weight of cyclohexane were added as a solvent, and the total solid content of the mixed solution was dissolved by stirring at a temperature of 50 ° C for 8 hours. A 6.5 wt% primer composition was prepared.

(비교예 2)(Comparative Example 2)

온도조절과 속도조절이 가능한 혼합용기에 열가소성 개질된 염화폴리올레핀 수지 5 중량%, 열가소성 폴리우레탄 수지(pearstic 45-50/18, MERQINSA) 1 중량%에 점착부여제(SU-120, 코오롱유화) 1 중량%를 첨가한 후 용제로써 메틸에틸케톤 50 중량%, 노말헥산 27 중량%, 사이클로헥산 16 중량%를 투입하여 50℃의 온도에서 8시간 교반하여 용해시킨 혼합액의 총고형분이 7 중량%인 프라이머 조성물을 제조하였다.
Tackifier (SU-120, Kolon Emulsifier) in 5% by weight of thermoplastically modified chlorinated polyolefin resin and 1% by weight of thermoplastic polyurethane resin (pearstic 45-50 / 18, MERQINSA) in a mixing vessel capable of temperature control and speed control 1 After adding the wt%, 50% by weight of methyl ethyl ketone, 27% by weight of normal hexane, and 16% by weight of cyclohexane were added as a solvent, and the mixture was stirred for 8 hours at a temperature of 50 ° C. The total solid content of the mixed solution was 7% by weight. The composition was prepared.

(비교예 3)(Comparative Example 3)

화승 T&C사에서 생산한 프라이머 제품인 PR-708을 사용하였다.
PR-708, a primer product produced by Hwaseung T & C, was used.

4. 난접착 신발 소재용 프라이머 조성물의 평가
4. Evaluation of primer composition for non-adhesive shoe material

상기 실시예 및 비교예에 의거하여 제조한 난접착 신발 소재용 프라이머 조성물 100 중량부에 대하여 경화제인 이소시아네이트 5 중량부를 혼합한 다음 생분해성 에틸렌비닐아세테이트 폼 부품에 적용하여 고무와의 접착력을 아래 방법에의해 평가하였으며 그 결과는 아래 [표 1]의 내용과 같다. 5 parts by weight of isocyanate, which is a curing agent, was mixed with respect to 100 parts by weight of the primer composition for the non-adhesive shoe material prepared according to the above Examples and Comparative Examples, and then applied to a biodegradable ethylene vinyl acetate foam part, thereby adhering the adhesive strength with the rubber to the following method. The results are summarized in [Table 1] below.

가, 생분해성 에틸렌비닐아세테이트 폼과 고무 시편의 접착Adhesion between Biodegradable Ethylene Vinyl Acetate Foam and Rubber Specimens

25×100mm의 크기의 기능성 에틸렌비닐아세테이트 폼 부품에 메틸에틸케톤으로 세척한 후 건조한 다음 상기 제조된 프라이머 100중량부에 대하여 경화제(동성화학 DRF) 5 중부를 혼합한 후 도포하고 60℃에서 5분간 건조하였다.After washing with methyl ethyl ketone on a functional ethylene vinyl acetate foam part having a size of 25 × 100 mm and drying, 5 parts by weight of a curing agent (Dynamic Chemical DRF) was mixed and applied to 100 parts by weight of the prepared primer, and applied at 60 ° C. for 5 minutes. Dried.

아울러, 고무 시트도 25×100mm의 크기로 준비하여 세척한 후 건조한 다음 고무용 프라이머(화승 T&C PR-700)를 도포한 후 60℃에서 5분간 건조하였다.In addition, the rubber sheet was also prepared in the size of 25 × 100mm, washed and dried, and then coated with a rubber primer (Hwaseung T & C PR-700) and dried at 60 ℃ for 5 minutes.

다음으로 위의 두 피착재에 접착제를 각각 도포한 후 60℃에서 5분간 건조한 후 접합하여 10kg의 하중으로 압착하여 접착하였다. 이때 동일 시험에 사용하는 시험 시편은 5개를 사용하였다.
Next, after applying the adhesive to each of the above two adherends, and then dried for 5 minutes at 60 ℃ and bonded by pressing with a load of 10kg. At this time, five test specimens used in the same test was used.

나, 초기 접착력 평가B, initial adhesion evaluation

제조된 접착시편을 실온에서 30분간 방치한 후 만능인장시험기를 사용하여 100mm/분의 인장속도로 박리하여 접착 강도를 측정하였다.
The prepared adhesive specimen was left at room temperature for 30 minutes, and then peeled at a tensile speed of 100 mm / min using a universal tensile tester to measure adhesive strength.

다, 상태 접착력 평가C, state adhesion evaluation

제조된 접착시편을 실온에서 24시간 방치한 후 만능인장시험기(UTM)를 사용하여 100mm/분의 인장속도로 박리하여 접착 강도를 측정하였다.
The prepared adhesive specimen was left at room temperature for 24 hours, and then peeled at a tensile speed of 100 mm / min using a universal tensile tester (UTM) to measure adhesive strength.

특성characteristic 실시예Example 비교예Comparative example 1One 22 33 44 1One 22 33 초기 접착력(kgf/cm)Initial Adhesion (kg f / cm) 2.92.9 2.82.8 2.92.9 2.52.5 3.13.1 1.81.8 2.62.6 상태 접착력(kgf/cm)Adhesive state (kg f / cm) 3.83.8 3.63.6 3.43.4 3.43.4 3.63.6 2.22.2 2.92.9 치수안정성Dimensional stability 양호Good 양호Good 양호Good 양호Good 양호Good 양호Good 불량Bad

상기 [표 1]에 나타난 바와 같이 본 발명에 따른 실시예 1 내지 4는 유해성 방향족 용제와 할로겐 함유 수지를 사용하지 않으면서도 비교예 1 내지 3에 비해 초기 접척력과 상태 접착력이 모두 우수하였으며, 특히 상태 접착력이 우수한 것으로 평가되었다. As shown in Table 1, Examples 1 to 4 according to the present invention were excellent in both the initial adhesive force and the state adhesive force, compared to Comparative Examples 1 to 3 without using a hazardous aromatic solvent and a halogen-containing resin, in particular It was evaluated that the state adhesion was excellent.

또한 비교예 3에 비하여 치수안정성이 현저히 향상되었으며, 접착력 또한 우수하게 나타났다.
In addition, compared with Comparative Example 3, the dimensional stability was significantly improved, the adhesion was also excellent.

상술한 바와 같이, 본 발명에 따른 비할로겐 타입 난접착 신발 소재용 프라이머 조성물을 상기의 바람직한 실시 예를 통해 설명하고, 그 우수성을 확인하였지만 해당 기술분야의 당업자라면 하기의 특허청구범위에 기재된 본 발명의 사상 및 영역으로부터 벗어나지 않는 범위 내에서 본 발명을 다양하게 수정 및 변경시킬 수 있음을 이해할 수 있을 것이다.As described above, the primer composition for non-halogen-type hard-adhesive shoe material according to the present invention has been described through the above-described preferred embodiments, and the superiority thereof has been confirmed, but those skilled in the art will appreciate the present invention described in the following claims. It will be understood that various modifications and changes can be made in the present invention without departing from the spirit and scope of the invention.

Claims (4)

난접착 신발 소재용 프라이머 조성물에 있어서,
폴리우레탄 아크릴레이트 수지 2~6 중량%, 열가소성 폴리우레탄 수지 1.0~2.5 중량%, 나노복합재 0.5~1.5 중량%, 점착 부여제 0.5~1.5 중량% 및 용제 88.5~96 중량%로 이루어진 것을 특징으로 하는 비할로겐 타입 난접착 신발 소재용 프라이머 조성물.
In the primer composition for hard-adhesive shoe material,
2 to 6 wt% of polyurethane acrylate resin, 1.0 to 2.5 wt% of thermoplastic polyurethane resin, 0.5 to 1.5 wt% of nanocomposite, 0.5 to 1.5 wt% of tackifier and 88.5 to 96 wt% of solvent Primer composition for non-halogen type, non-adhesive shoe material.
제 1항에 있어서,
상기 폴리우레탄 아크릴레이트 수지는,
말단에 수산기를 가지고 있는 폴리카프로락톤 35~45 몰%에 디이소시아네이트 50 몰%를 사용하여 말단에 수산기를 포함하는 폴리우레탄 프리폴리머를 제조하고, 사슬연장제로 하이드록시에틸 메타크릴레이트를 5~15 몰% 사용하여 합성한 폴리우레탄 아크릴레이트 화합물을 사용하는 것을 특징으로하는 비할로겐 타입 난접착 신발 소재용 프라이머 조성물.
The method of claim 1,
The polyurethane acrylate resin,
To prepare a polyurethane prepolymer containing a hydroxyl group at the terminal using 35 to 45 mol% of polycaprolactone having a hydroxyl group at the end and 50 mol% of diisocyanate, and 5 to 15 mol of hydroxyethyl methacrylate as a chain extender. A primer composition for a non-halogen type hard-adhesive shoe material, characterized in that a polyurethane acrylate compound synthesized using% is used.
제 1항에 있어서,
상기 나노복합재는,
PEGMA/(Na-MMT)-co-MMA/MA 나노복합재로써, 폴리(에틸렌 글리콜) 메틸 에테르 메타크릴레이트(PEGMA, Poly(ethylene glycol) methyl ether methacrylate)를 소듐 몬모릴로나이트(Na-MMT, Na-montmorillonite)의 층간에 삽입한 후,
메타크릴산메틸(MMA, Methyl Methacrylate) 및 아크릴산메틸(MA, Methyl Acrylate) 단량체와의 공중합시킨 것을 특징으로 하는 비할로겐 타입 난접착 신발 소재용 프라이머 조성물.
The method of claim 1,
The nanocomposite,
As a PEGMA / (Na-MMT) -co-MMA / MA nanocomposite, poly (ethylene glycol) methyl ether methacrylate (PEGMA) is converted to sodium montmorillonite (Na-MMT, Na-montmorillonite). Between the layers of
Primer composition for a non-halogen type hard-adhesive shoe material, characterized in that copolymerized with methyl methacrylate (MMA, Methyl Methacrylate) and methyl acrylate (MA, Methyl Acrylate) monomer.
제 1항에 있어서,
상기 용제는,
노말 헥산, 에틸아세테이트, 메틸에틸케톤, 아세톤, 이소프로필알콜, 에탄올, 메탄올, 싸이클로헥산, 메틸싸이클로헥산으로 이루어진 군에서 3종 이상 병용하여 사용하는 것을 특징으로 하는 비할로겐 타입 난접착 신발 소재용 프라이머 조성물.
The method of claim 1,
The solvent,
Primer for non-halogen type hard-adhesive shoe material, characterized in that used in combination of three or more in the group consisting of normal hexane, ethyl acetate, methyl ethyl ketone, acetone, isopropyl alcohol, ethanol, methanol, cyclohexane, methyl cyclohexane Composition.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106349959A (en) * 2016-08-21 2017-01-25 马爱芬 Adhesion enhancer for polyurethane and preparation method, application and use method of adhesion enhancer
KR20200059009A (en) * 2018-11-20 2020-05-28 한국신발피혁연구원 Primer composition for polycarbonate material
CN111286297A (en) * 2020-02-28 2020-06-16 天津斯多福新材料研发有限公司 High-strength ultraviolet/moisture dual-curing adhesive and preparation method and use method thereof

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101061073B1 (en) * 2008-12-30 2011-08-31 한국신발피혁연구소 Adhesion Reinforcement Primer Composition
KR101108549B1 (en) * 2009-03-10 2012-01-31 한국신발피혁연구소 Composition of water based primer for vulcanizing shoes
KR101157113B1 (en) * 2010-03-15 2012-06-22 한국신발피혁연구소 Primer compositions for thermoplastic polyurethane elastomer
KR101297673B1 (en) * 2011-04-26 2013-08-21 한국신발피혁연구원 Primer composition for difficulty adhesion shoe material

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106349959A (en) * 2016-08-21 2017-01-25 马爱芬 Adhesion enhancer for polyurethane and preparation method, application and use method of adhesion enhancer
KR20200059009A (en) * 2018-11-20 2020-05-28 한국신발피혁연구원 Primer composition for polycarbonate material
CN111286297A (en) * 2020-02-28 2020-06-16 天津斯多福新材料研发有限公司 High-strength ultraviolet/moisture dual-curing adhesive and preparation method and use method thereof

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