KR102262833B1 - Polyurea crack reinforcing agent and reinforcing, waterprofing and protecting against corrosion using thereof - Google Patents

Polyurea crack reinforcing agent and reinforcing, waterprofing and protecting against corrosion using thereof Download PDF

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KR102262833B1
KR102262833B1 KR1020200188293A KR20200188293A KR102262833B1 KR 102262833 B1 KR102262833 B1 KR 102262833B1 KR 1020200188293 A KR1020200188293 A KR 1020200188293A KR 20200188293 A KR20200188293 A KR 20200188293A KR 102262833 B1 KR102262833 B1 KR 102262833B1
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이미경
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    • 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
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    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
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    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30Low-molecular-weight compounds
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    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
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    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
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    • C08G18/00Polymeric products of isocyanates or isothiocyanates
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    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
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    • C08G18/74Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/76Polyisocyanates or polyisothiocyanates cyclic aromatic
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Abstract

According to the present invention, provided is a crack repair agent using polyurea, including: a polyurea solution (A) prepared by mixing isocyanurate with shodium lactate ethylsilanol, 1,5-naphthalene diisocyanate, methyl vinyl ether, aluminum chloride and polyoxyethylene linoleate; and a curing agent solution (B) prepared by mixing iodobenzene with phenylhydrazine, cetylalcohol ethylene propylene copolymer, cyclopentane and diethyl ether.

Description

폴리우레아를 이용한 균열보수제 및 이를 이용한 도장, 방수 및 방식 공법{Polyurea crack reinforcing agent and reinforcing, waterprofing and protecting against corrosion using thereof}Polyurea crack reinforcing agent and coating, waterproofing and anticorrosive method using polyurea {Polyurea crack reinforcing agent and reinforcing, waterprofing and protecting against corrosion using thereof}

본 발명은 폴리우레아를 이용한 균열보수제 및 이를 이용한 도장, 방수 및 방식 공법에 관한 것으로서, 보다 상세하게는, 이소시아누레이트, 쇼듐락테이트메틸실란올, 1,5-나프탈렌디이소시아네이트, 메틸비닐에테르, 알루미늄클로라이드 및 폴리옥시에틸렌리놀레이트를 혼합하여 폴리우레아 A액을 제조하고, 아이오도벤젠, 페닐하이드라진, 세틸알콜에틸렌프로필렌코폴리머, 싸이클로펜탄 및 디에틸에테르를 혼합하여 경화제 B액을 제조한 후, A액과 B액을 소정의 부피비로 혼합한 폴리우레아를 이용한 균열보수제 및 이를 이용한 도장, 방수 및 방식 공법에 관한 것이다.The present invention relates to a crack repair agent using polyurea and a coating, waterproofing and anticorrosive method using the same, and more particularly, isocyanurate, shodium lactate methylsilanol, 1,5-naphthalene diisocyanate, methyl vinyl ether , aluminum chloride and polyoxyethylene linoleate to prepare polyurea solution A, iodobenzene, phenylhydrazine, cetyl alcohol ethylene propylene copolymer, cyclopentane and diethyl ether were mixed to prepare curing agent solution B , It relates to a crack repair agent using polyurea mixed with solution A and solution B in a predetermined volume ratio, and to a coating, waterproofing and anticorrosive method using the same.

콘크리트 구조물의 수분에 의한 부식이나 파손 등을 방지하기 위해서는 콘크리트 구조물 표면에 방수 또는 방식 처리를 하는 것이 요구된다. 이러한 방수 처리는 일반적으로 방수용 수지를 콘크리트 구조물의 표면에 도포함으로서 이루어진다.In order to prevent corrosion or damage caused by moisture in the concrete structure, it is required to waterproof or anticorrosive the surface of the concrete structure. This waterproofing treatment is generally made by applying a waterproofing resin to the surface of the concrete structure.

종래 일반적인 콘크리트 구조물 표면의 방수 공법은, 등록특허 10-1215403호 등에 개시된 바와 같이, 방수하고자 하는 구조물의 표면에 묻은 오염물을 제거하고 평탄화하는 전처리 단계와, 상기 전처리된 표면에 프라이머를 코팅하여 프라이머층을 형성하는 단계 및 상기 프라이머층 상에 폴리우레아를 도포하는 단계를 포함하여 이루어진다.As disclosed in Korean Patent Registration No. 10-1215403, a conventional general method for waterproofing the surface of a concrete structure includes a pretreatment step of removing and planarizing contaminants on the surface of a structure to be waterproofed, and coating a primer on the pretreated surface to form a primer layer. It consists of forming and applying polyurea on the primer layer.

이러한 폴리우레아의 분자는 보통의 경우 유연성을 크게 하는 요소와 경도를 크게 하는 요소들이 고르게 분포되어 있는 상태로 구성되어 있다.In general, these molecules of polyurea are composed of factors that increase flexibility and factors that increase hardness are evenly distributed.

일반적으로 알려진 바에 의하면, 유연성을 크게 하는 요소는 낮은 유리전이온도를 갖는 것으로 폴리에테르, 폴리에스테르, 폴리알킬디올 등으로 중량 평균분자량이 400-5000 사이일 때 유연성이 커지고, 경도를 크게 하려면 높은 Tg를 갖고 있으며 준결정성의 방향족 디이소시아네이트가 낮은 분자량의 사슬 확장자에 결합하면 경도가 커진다.As is generally known, the factor that increases flexibility is that it has a low glass transition temperature, such as polyether, polyester, polyalkyldiol, etc., which increases flexibility when the weight average molecular weight is between 400 and 5000, and high Tg to increase hardness. When the semi-crystalline aromatic diisocyanate binds to a low molecular weight chain extender, the hardness increases.

일반적으로 폴리우레아는 사슬 확장자와 낮은 분자량 을 갖는 디아민류와 합성되어 우레아 단위체를 만드는 것이다. 따라서 폴리우레아는 선택된 물질이나 분자량, 또는 반응되는 비율 등의 기타 다양한 요소에 의하여 그 성질이 폭 넓게 변화되어 나타난다. 즉, 그 성질이 부스러지기 쉬운 물질에서 단단한 물질 또는 부드러운 물질, 더 나아가서는 어떤 점성을 갖는 물질로 변화가 가능하다. 특히 폴리우레아의 경우에는 지방산의 아미드 에스테르 결합이 혼합된 결합을 가지므로 고온에서의 성질은 이들 폴리에스테르계와 폴리아미드계의 중간적 성질을 가지고 있다.In general, polyurea is synthesized with diamines having a chain extension and low molecular weight to make a urea unit. Accordingly, the properties of polyurea are widely changed depending on the selected material, molecular weight, or other various factors such as the reaction ratio. That is, it is possible to change its properties from a brittle material to a hard material or a soft material, and furthermore, to a material having a certain viscosity. In particular, in the case of polyurea, since the amide ester bonds of fatty acids have mixed bonds, the properties at high temperatures have intermediate properties between those polyesters and polyamides.

폴리우레아의 합성은 부가반응과 축합반응의 두 개의 큰 영역으로 구분할 수 있다. 부가반응은 불포화 단량체가 반응 개시 단계, 전개 단계, 종결 단계에서 반응하여 일어난다. 보통 단량체들은 이중결합을 가지고 있는 간단한 분자들인데 개시단계에서 두 개의 이중결합 중 하나가 깨지면서 반응 하는데 미반응 단량체가 거의 희박할 때까지 빠르게 반응이 진행된다.The synthesis of polyurea can be divided into two large areas: addition reaction and condensation reaction. The addition reaction occurs when the unsaturated monomer reacts in the reaction initiation stage, development stage, and termination stage. Usually, monomers are simple molecules with double bonds, and in the initiation stage, one of the two double bonds is broken and the reaction proceeds rapidly until the unreacted monomer is almost lean.

대부분의 경우 부가반응은 부생산물을 만들지 않고 진행된다. 축합 또는 단계적 성장 반응은 단량체들이 고분자의 사슬을 형성하기 위해 만들어진 단계에서 이중 작용기를 갖는 분자와 반응할 때 일어난다. 이는 작은 분자량을 갖는 분자들 간의 축합반응과 유사하다. 이때 작은 분자인 물이나 이산화탄소 같은 물질은 제거되기도 한다.In most cases, the addition reaction proceeds without the formation of by-products. A condensation or step-growth reaction occurs when monomers react with a molecule with a double functional group in a step made to form a chain of a polymer. This is similar to a condensation reaction between molecules having a small molecular weight. At this time, substances such as water and carbon dioxide, which are small molecules, are also removed.

부가반응은 균일 고분자나 공중합체로 구분할 수 있는데, 공중합체의 미세한 형태는 무작위, 교차, 덩어리 형태로 나눌 수 있지만 이는 반응 조건이나 농도, 단량체의 반응성 비율 등에 따라 차이가 있다. 더군다나 최종 반응 생성물인 고분자들의 반응 후 분자량이나 분자량의 분포 등을 제어하는 것은 사슬 형태를 변화시키는 시약을 사용하여 제어하는 축합반응보다도 더 어려운 것이다. 반응성의 조절은 음이온 고분자화법에 의해 조절될 수 있고 어떤 경우에는 거의 단일 연쇄상 분포의 합성도 가능하다. 축합반응은 공중합 고분자물질을 만들 때도 사용 된다. 이중 작용기를 갖는 단량체 들은 사슬형 고분자를 만들기 위해 이용되고 삼중 이상의 작용기를 갖는 것은 삼차원적 공간에 교차 결합 고분자 망을 구성할 수도 있다.The addition reaction can be divided into homogeneous polymers or copolymers. The microscopic form of the copolymer can be divided into random, crossed, and lumped forms, but there are differences depending on the reaction conditions, concentration, and the reactivity ratio of the monomers. Moreover, it is more difficult to control the molecular weight or molecular weight distribution after the reaction of polymers, which are final reaction products, than the condensation reaction controlled using a reagent that changes the chain shape. The control of reactivity can be controlled by anionic polymerisation, and in some cases the synthesis of nearly single chain distributions is possible. Condensation reaction is also used to make copolymer polymer materials. Monomers having double functional groups are used to make chain polymers, and those having triple or more functional groups can form a cross-linked polymer network in three-dimensional space.

폴리우레아는 관능기를 갖는 폴리옥시에테르 폴리아민 혼합물과 이소시아네이트 프리폴리머의 반응으로 형성되는 엘라스토머 특성을 갖는 고분자 물질로 아민과 이소시아네이트의 급속한 반응성 때문에, 일반적으로 상온에서 혼합하여 사용할 수 없으며 특수한 스프레이 장비를 이용하여 도장작업을 진행한다. 그리고 폴리우레아는 합성고무와 같은 엘라스토머 성질을 가지므로 난연성이 저조하여 화재에 취약한 문제점을 가지고 있다. Polyurea is a high molecular material with elastomeric properties formed by the reaction of a polyoxyether polyamine mixture having a functional group and an isocyanate prepolymer. Because of the rapid reactivity of amine and isocyanate, it cannot be generally mixed and used at room temperature. proceed with the work And since polyurea has the same elastomeric properties as synthetic rubber, it has low flame retardancy and is vulnerable to fire.

따라서 본 발명의 목적은 이소시아누레이트, 쇼듐락테이트메틸실란올, 1,5-나프탈렌디이소시아네이트, 메틸비닐에테르, 알루미늄클로라이드 및 폴리옥시에틸렌리놀레이트를 혼합하여 폴리우레아 A액을 제조하고, 아이오도벤젠, 페닐하이드라진, 세틸알콜에틸렌프로필렌코폴리머, 싸이클로펜탄 및 디에틸에테르를 혼합하여 경화제 B액을 제조한 후, A액과 B액을 소정의 부피비로 혼합한 폴리우레아를 이용한 균열보수제 및 이를 이용한 도장, 방수 및 방식 공법을 제공하는 것이다. Therefore, an object of the present invention is to prepare a polyurea solution A by mixing isocyanurate, shodium lactate methylsilanol, 1,5-naphthalene diisocyanate, methyl vinyl ether, aluminum chloride and polyoxyethylene linoleate, and iodine After preparing curing agent solution B by mixing dobenzene, phenylhydrazine, cetyl alcohol ethylene propylene copolymer, cyclopentane and diethyl ether, a crack repair agent using polyurea obtained by mixing solution A and solution B in a predetermined volume ratio, and this It is to provide a coating, waterproofing and anticorrosive construction method using.

한편, 본 발명의 목적은 이상에서 언급한 목적으로 제한되지 않으며, 언급되지 않은 다른 목적들은 아래의 기재로부터 통상의 기술자에게 명확하게 이해될 수 있을 것이다.On the other hand, the object of the present invention is not limited to the object mentioned above, and other objects not mentioned will be clearly understood by those skilled in the art from the following description.

이를 위하여, 본 발명에 의하면, 이소시아누레이트에 쇼듐락테이트메틸실란올, 1,5-나프탈렌디이소시아네이트, 메틸비닐에테르, 알루미늄클로라이드 및 폴리옥시에틸렌리놀레이트가 혼합되어 제조되는 폴리우레아 A액과; 아이오도벤젠에 페닐하이드라진, 세틸알콜에틸렌프로필렌코폴리머, 싸이클로펜탄 및 디에틸에테르가 혼합되어 제조되는 경화제 B액을 포함하는 폴리우레아를 이용한 균열보수제가 제공된다.To this end, according to the present invention, polyurea solution A prepared by mixing isocyanurate with shodium lactate methylsilanol, 1,5-naphthalene diisocyanate, methyl vinyl ether, aluminum chloride and polyoxyethylene linoleate, and ; There is provided a crack repair agent using polyurea containing a curing agent B solution prepared by mixing iodobenzene with phenylhydrazine, cetyl alcohol ethylene propylene copolymer, cyclopentane and diethyl ether.

여기서, A액은, 이소시아누레이트 100 중량부에 쇼듐락테이트메틸실란올 70-80 중량부, 1,5-나프탈렌디이소시아네이트 60-70 중량부, 메틸비닐에테르 50-60 중량부, 알루미늄클로라이드 40-50 중량부 및 폴리옥시에틸렌리놀레이트 20-30 중량부가 혼합되고 80℃-120℃의 온도에서 승온된 후 5-7시간 반응되어 제조되는 것이 바람직하다.Here, solution A is 70-80 parts by weight of shodium lactate methylsilanol, 60-70 parts by weight of 1,5-naphthalene diisocyanate, 50-60 parts by weight of methyl vinyl ether, aluminum chloride in 100 parts by weight of isocyanurate. It is preferable that 40-50 parts by weight and 20-30 parts by weight of polyoxyethylene linoleate are mixed and reacted for 5-7 hours after heating at a temperature of 80°C-120°C.

또한, B액은, 아이오도벤젠 100 중량부에 페닐하이드라진 50-60 중량부, 세틸알콜에틸렌프로필렌코폴리머 40-50 중량부, 싸이클로펜탄 30-40 중량부 및 디에틸에테르 10-20 중량부가 혼합되어 제조되는 것이 바람직하다.In addition, liquid B is mixed with 100 parts by weight of iodobenzene, 50-60 parts by weight of phenylhydrazine, 40-50 parts by weight of cetyl alcohol ethylene propylene copolymer, 30-40 parts by weight of cyclopentane, and 10-20 parts by weight of diethyl ether. It is preferable to be manufactured.

또한, A액과 B액은 5:5 내지 7:3의 부피비로 혼합되어 제조되는 것이 바람직하다.In addition, it is preferable that the liquid A and the liquid B are prepared by mixing in a volume ratio of 5:5 to 7:3.

한편, 본 발명에 의하면, 시공 표면이 전처리되는 단계와; 상기와 같은 폴리우레아를 이용한 균열보수제가 제조되는 단계와; 도포 또는 분사수단에 의해 상기 시공 표면에 소정의 두께로 폴리우레아를 이용한 균열제가 도포 또는 분사되는 단계를 포함하는 폴리우레아를 이용한 균열보수제를 이용한 도장, 방수 및 방식 공법이 제공된다. On the other hand, according to the present invention, the step of pre-treatment of the construction surface; manufacturing a crack repair agent using polyurea as described above; There is provided a painting, waterproofing and anticorrosive method using a crack repair agent using polyurea, which includes the step of applying or spraying a cracking agent using polyurea to a predetermined thickness on the construction surface by an application or spraying means.

따라서 본 발명에 의하면, 이소시아누레이트, 쇼듐락테이트메틸실란올, 1,5-나프탈렌디이소시아네이트, 메틸비닐에테르, 알루미늄클로라이드 및 폴리옥시에틸렌리놀레이트를 혼합하여 폴리우레아 A액을 제조하고, 아이오도벤젠, 페닐하이드라진, 세틸알콜에틸렌프로필렌코폴리머, 싸이클로펜탄 및 디에틸에테르를 혼합하여 경화제 B액을 제조한 후, A액과 B액을 소정의 부피비로 혼합한 보수성, 방수성 및 방식성이 우수한 보강을 가능하게 할 수 있다.Therefore, according to the present invention, polyurea solution A is prepared by mixing isocyanurate, shodium lactate methylsilanol, 1,5-naphthalene diisocyanate, methyl vinyl ether, aluminum chloride and polyoxyethylene linoleate, and iodine Dobenzene, phenylhydrazine, cetyl alcohol ethylene propylene copolymer, cyclopentane and diethyl ether were mixed to prepare curing agent solution B, and then solution A and solution B were mixed in a predetermined volume ratio to provide excellent water retention, waterproof and corrosion resistance. reinforcement may be possible.

한편, 본 발명의 효과는 이상에서 언급한 효과로 제한되지 않으며, 언급되지 않은 다른 효과들은 청구범위의 기재로부터 통상의 기술자에게 명확하게 이해될 수 있을 것이다.On the other hand, the effects of the present invention are not limited to the effects mentioned above, and other effects not mentioned will be clearly understood by those skilled in the art from the description of the claims.

이하, 본 발명의 바람직한 실시예에 대하여 상세히 설명하기로 한다. Hereinafter, preferred embodiments of the present invention will be described in detail.

본 발명의 바람직한 실시예에 따른 폴리우레아를 이용한 균열보수제는, 기본적으로, 이소시아누레이트에 쇼듐락테이트메틸실란올, 1,5-나프탈렌디이소시아네이트, 메틸비닐에테르, 알루미늄클로라이드 및 폴리옥시에틸렌리놀레이트가 혼합되어 제조되는 폴리우레아 A액과, 아이오도벤젠에 페닐하이드라진, 세틸알콜에틸렌프로필렌코폴리머, 싸이클로펜탄 및 디에틸에테르가 혼합되어 제조되는 경화제 B액이 소정의 부피비로 혼합되어 제조된다.The crack repair agent using polyurea according to a preferred embodiment of the present invention is basically, isocyanurate, shodium lactate methylsilanol, 1,5-naphthalenediisocyanate, methyl vinyl ether, aluminum chloride and polyoxyethylene linol. Polyurea solution A prepared by mixing the rate, and curing agent solution B prepared by mixing iodobenzene with phenylhydrazine, cetyl alcohol ethylene propylene copolymer, cyclopentane and diethyl ether is prepared by mixing in a predetermined volume ratio.

구제처적으로, 본 발명의 폴리우레아를 이용한 균열보수제는, 이소시아누레이트 100 중량부에 쇼듐락테이트메틸실란올 70-80 중량부, 1,5-나프탈렌디이소시아네이트 60-70 중량부, 메틸비닐에테르 50-60 중량부, 알루미늄클로라이드 40-50 중량부 및 폴리옥시에틸렌리놀레이트 20-30 중량부가 혼합되고 80℃-120℃의 온도에서 승온된 후 5-7시간 반응되어 폴리우레아 A액이 제조되고, 아이오도벤젠 100 중량부에 페닐하이드라진 50-60 중량부, 세틸알콜에틸렌프로필렌코폴리머 40-50 중량부, 싸이클로펜탄 30-40 중량부 및 디에틸에테르 10-20 중량부가 혼합되어 경화제 B액이 제조된 후, 상기 A액과 B액이 5:5 내지 7:3의 부피비로 혼합되어 제조된다.As a remedy, the crack repair agent using polyurea of the present invention is 70-80 parts by weight of shodium lactate methylsilanol, 60-70 parts by weight of 1,5-naphthalene diisocyanate, methylvinyl in 100 parts by weight of isocyanurate. 50-60 parts by weight of ether, 40-50 parts by weight of aluminum chloride, and 20-30 parts by weight of polyoxyethylene linoleate are mixed, heated at a temperature of 80°C-120°C, and reacted for 5-7 hours to prepare polyurea solution A and 50-60 parts by weight of phenylhydrazine, 40-50 parts by weight of cetyl alcohol ethylene propylene copolymer, 30-40 parts by weight of cyclopentane, and 10-20 parts by weight of diethyl ether are mixed with 100 parts by weight of iodobenzene, curing agent B solution After this preparation, the liquid A and the liquid B are prepared by mixing in a volume ratio of 5:5 to 7:3.

여기서, 상기 A액의 조성물들의 중량부는 이소시아누레이트 100중량부를 기준으로 하고, 상기 B액의 조성물들의 중량부는 아이오도벤젠 100중량부를 기준으로 한다.Here, the parts by weight of the compositions of the solution A are based on 100 parts by weight of isocyanurate, and the parts by weight of the compositions of the solution B are based on 100 parts by weight of iodobenzene.

한편, 본 발명의 바람직한 실시예에 따른 폴리우레아를 이용한 균열보수제의 제조방법은, 이소시아누레이트 100 중량부에 쇼듐락테이트메틸실란올 70-80 중량부, 1,5-나프탈렌디이소시아네이트 60-70 중량부, 메틸비닐에테르 50-60 중량부, 알루미늄클로라이드 40-50 중량부 및 폴리옥시에틸렌리놀레이트 20-30 중량부가 혼합되고 80℃-120℃의 온도에서 승온된 후 5-7시간 반응되어 폴리우레아 A액이 제조되는 단계와, 아이오도벤젠 100 중량부에 페닐하이드라진 50-60 중량부, 세틸알콜에틸렌프로필렌코폴리머 40-50 중량부, 싸이클로펜탄 30-40 중량부 및 디에틸에테르 10-20 중량부가 혼합되어 경화제 B액이 제조되는 단계와, 상기 A액과 B액이 5:5 내지 7:3의 부피비로 혼합되는 단계를 포함한다.On the other hand, in the method for producing a crack repair agent using polyurea according to a preferred embodiment of the present invention, 70-80 parts by weight of shodium lactate methylsilanol, 60- 1,5-naphthalene diisocyanate in 100 parts by weight of isocyanurate 70 parts by weight, 50-60 parts by weight of methyl vinyl ether, 40-50 parts by weight of aluminum chloride, and 20-30 parts by weight of polyoxyethylene linoleate are mixed, heated at a temperature of 80°C-120°C, and reacted for 5-7 hours A step of preparing a polyurea solution A, and 50-60 parts by weight of phenylhydrazine, 40-50 parts by weight of cetyl alcohol ethylene propylene copolymer, 30-40 parts by weight of cyclopentane, and 10 parts by weight of diethyl ether in 100 parts by weight of iodobenzene 20 parts by weight are mixed to prepare a curing agent solution B, and the solution A and solution B are mixed in a volume ratio of 5:5 to 7:3.

여기서, 상기 A액의 조성물들의 중량부는 이소시아누레이트 100중량부를 기준으로 하고, 상기 B액의 조성물들의 중량부는 아이오도벤젠 100중량부를 기준으로 한다.Here, the parts by weight of the compositions of the solution A are based on 100 parts by weight of isocyanurate, and the parts by weight of the compositions of the solution B are based on 100 parts by weight of iodobenzene.

이소시아누레이트는, 콘크리트 등과 같은 균열부위에 흡착 및 접착 기능을 제공하는 물질로서, 상기 주제인 A액과 경화제인 B액의 혼합물 또는 조성물의 반응속도를 빠르게 하여 단시간 내에 상기 혼합물들이 프리폴리머로 전환되도록 하고 반응을 종결시키는 기능을 수행한다. Isocyanurate is a material that provides adsorption and adhesion to cracks such as concrete, etc., and it speeds up the reaction rate of a mixture or composition of the subject A solution and the curing agent B solution, so that the mixture is converted into a prepolymer within a short time. It serves the function of terminating the reaction.

쇼듐락테이트메틸실란올은, 상기 조성물들과의 반응 시간을 결정하고 흡착 기능을 제공하는 물질로서, 상기 이소시아누레이트 100 중량부를 기준으로 70-80 중량부가 혼합되는데, 상기 중량부를 초과하는 경우에는 상기 조성물들의 반응속도가 너무 빨라지게 되어 교반성 및 시공성이 저하되고, 상기 중량부를 미만하는 경우에는 상기 조성물들의 반응속도가 너무 느려지게 되어 작업 시간이 증가하게 되는 문제점이 있으므로, 상기와 같은 한정된 범위의 중량부가 유지되는 것이 바람직하다.Shodium lactate methylsilanol is a material that determines the reaction time with the above compositions and provides an adsorption function, and is mixed in 70-80 parts by weight based on 100 parts by weight of the isocyanurate, but when it exceeds the above weight, Since the reaction rate of the compositions is too fast, the stirrability and workability are lowered, and when the amount is less than the above weight part, the reaction rate of the compositions becomes too slow and the working time increases. It is preferred that parts by weight of the range be maintained.

1,5-나프탈렌디이소시아네이트는, 상기 조성물들과 반응하여 도막층을 형성하는 물질로서, 상기 이소시아누레이트 100 중량부를 기준으로 60-70 중량부가 혼합되는데, 상기 중량부를 초과하는 경우에는 점성이 너무 커지게 되어 시공성이 저하되고, 상기 중량부를 미만하는 경우에는 접착 강도가 저하되는 문제점이 있으므로, 상기와 같은 한정된 범위의 중량부가 유지되는 것이 바람직하다.1,5-naphthalene diisocyanate is a material that reacts with the above compositions to form a coating layer, and 60-70 parts by weight is mixed based on 100 parts by weight of the isocyanurate. Since it becomes too large and the workability is reduced, and if it is less than the said weight part, there exists a problem that adhesive strength is reduced, it is preferable to maintain the weight part in the limited range as mentioned above.

메틸비닐에테르는, 도막의 접착 강도 즉, 기계적 특성을 향상시키는 기능을 결정하는 물질로서, 상기 이소시아누레이트 100 중량부를 기준으로 50-60 중량부가 혼합되는데, 상기 중량부를 초과하는 경우에는 상기 복합물의 점도가 높아지게 되어 교반 작업이 불편해지고, 상기 중량부를 미만하는 경우에는 복합물의 저장 안정성이 저조하게 되어 도막층의 접착 강도가 저하되는 문제점이 있으므로, 상기와 같은 한정된 범위의 중량부가 유지되는 것이 바람직하다.Methyl vinyl ether is a material that determines the function of improving the adhesive strength of the coating film, that is, mechanical properties, and 50-60 parts by weight is mixed based on 100 parts by weight of the isocyanurate. Since the viscosity of is increased, stirring operation is inconvenient, and when the amount is less than the above weight part, the storage stability of the composite is poor and the adhesive strength of the coating layer is lowered. Therefore, it is preferable to maintain the weight part in the limited range as described above. Do.

알루미늄클로라이드는, 콘크리트 등과 같은 균열부위에 접착력을 제공하는 물질로서, 상기 이소시아누레이트 100 중량부를 기준으로 40-50 중량부가 혼합되는데, 상기 중량부를 초과하는 경우에는 A액의 전반적인 접착력은 강해지나 작업성이 저하되고, 상기 중량부를 미만하는 경우에는 콘크리트 표면으로부터 쉽게 박리되는 문제점이 있으므로, 상기와 같은 범위의 중량부가 유지되는 것이 바람직하다.Aluminum chloride is a material that provides adhesion to cracks such as concrete, and 40-50 parts by weight is mixed based on 100 parts by weight of the isocyanurate. Since workability is deteriorated, and since there is a problem in that the workability is easily peeled off from the concrete surface when it is less than the above weight part, it is preferable to maintain the weight part in the above range.

폴리옥시에틸렌리놀레이트는, A액과 B액의 혼합시 조성물들의 확산 및 기초가 제거되도록 하여 교반 효율이 향상되도록 하는 물질로서, 상기 이소시아누레이트 100 중량부를 기준으로 20-30 중량부가 혼합되는데, 상기 중량부를 벗어나는 경우 보수, 방수 및 방식을 위한 균열보수제의 전반적인 점도와 혼합율 등의 물리적 특성이 저하되므로, 상기와 같은 범위의 중량부가 유지되는 것이 바람직하다.Polyoxyethylene linoleate is a material that improves agitation efficiency by allowing the diffusion and base of the compositions to be removed when mixing solution A and solution B. 20-30 parts by weight is mixed based on 100 parts by weight of isocyanurate. , since physical properties such as overall viscosity and mixing ratio of the crack repair agent for repair, waterproofing and anticorrosion are lowered when it is out of the above weight part, it is preferable that the weight part in the above range is maintained.

한편, 상기 A액은, 이소시아누레이트에 쇼듐락테이트메틸실란올, 1,5-나프탈렌디이소시아네이트, 메틸비닐에테르, 알루미늄클로라이드 및 폴리옥시에틸렌리놀레이트가 혼합된 후, 80℃-120℃의 온도로 승온되고 5-7시간 반응되어 제조되도록 하고 있다.On the other hand, the liquid A is isocyanurate, after mixing shodium lactate methylsilanol, 1,5-naphthalene diisocyanate, methyl vinyl ether, aluminum chloride and polyoxyethylene linoleate, 80 ℃-120 ℃ It is heated to a temperature and reacted for 5-7 hours to be prepared.

여기서, 상기 A액의 조성물들이 혼합 및 적하되는 온도를 80℃-120℃로 한정하는 것은, 적하온도 즉, 교반온도가 상기 온도보다 낮으면 팽윤율이 저하되고, 교반온도가 상기 온도보다 높으면 과팽윤이 발생되므로, 상기와 같은 한정된 범위의 교반온도가 유지되는 것이 바람직하다. Here, limiting the temperature at which the compositions of the liquid A are mixed and dropped to 80° C.-120° C. is the dropping temperature, that is, when the stirring temperature is lower than the above temperature, the swelling rate is lowered, and when the stirring temperature is higher than the above temperature, and Since swelling occurs, it is preferable to maintain the stirring temperature in the limited range as described above.

또한, 상기 A액의 조성물들이 적하되는 시간이 5-7시간으로 한정하는 것은, 적하시간 즉, 교반시간이 상기 시간 보다 짧으면 팽윤이 잘 안되고, 교반시간이 상기 시간보다 길면 고증점이 되는 문제점이 있으므로, 상기와 같은 한정된 범위의 교반시간이 유지되는 것이 바람직하다.In addition, limiting the time for which the compositions of the solution A are dropped to 5-7 hours is that, if the dropping time, that is, the stirring time is shorter than the above time, the swelling is not good, and if the stirring time is longer than the above time, there is a problem that the viscosity is high. , it is preferable that the stirring time in the limited range as described above is maintained.

아이오도벤젠은, 도막 방수 시공시 부착력 증대와 보관시 층분리 현상을 방지하여 방수성을 제공하는 2액 가교형 합성수지도료이다.Iodobenzene is a two-component cross-linked synthetic resin coating that provides waterproofness by increasing adhesion during waterproofing and preventing layer separation during storage.

페닐하이드라진은, 도막 방수 시공시 A액과 B액의 조성물들이 신속하게 경화되도록 하는 물질로서, 상기 아이오도벤젠 100 중량부를 기준으로 50-60 중량부가 혼합되는데, 상기 중량부 보다 적게 혼합되면 경화제의 주요 성분인 폴리머가 주제인 A액과 혼합되기도 전에 보관 중 A액에 안료 성질이 포함되는 경우 안료 성질의 조성물과 반응되어 경화되고, 상기 중량부 보다 많이 혼합되면 주제인 A액과의 혼합시 교반 효율이 저하되는 문제점이 있으므로, 상기와 같은 한정된 중량부를 가지는 것이 바람직하다. Phenylhydrazine is a material that allows the compositions of solution A and solution B to cure quickly when waterproofing the coating film, and 50-60 parts by weight is mixed based on 100 parts by weight of the iodobenzene. If the main component polymer contains pigment properties during storage even before being mixed with the main component A solution, it reacts with the pigment property composition and hardens, and when mixed with the main component A solution, it is stirred when mixed with more than the above weight part Since there is a problem that the efficiency is lowered, it is preferable to have a limited weight part as described above.

세틸알콜에틸렌프로필렌코폴리머는, 상기 페닐하이드라진과 함께 도막 방수 시공시 초고속 경화가 이루어지도록 하는 물질로서, 상기 아이오도벤젠 100 중량부를 기준으로 40-50중량부가 혼합되는데, 상기 중량부 보다 적게 혼합되면 교반성이 저하되고, 상기 중량부 보다 많이 혼합되면 결합력이 증대되어 A액과의 혼합성이 저하되는 문제점이 있으므로, 상기와 같은 한정된 중량부를 가지는 것이 바람직하다. The cetyl alcohol ethylene propylene copolymer is a material for super-fast curing when waterproofing a coating film together with the phenylhydrazine, and 40-50 parts by weight is mixed based on 100 parts by weight of the iodobenzene. Since there is a problem in that the stirrability is lowered, and the mixing force is increased and the miscibility with the solution A is reduced when the mixture is mixed more than the above weight parts, it is preferable to have the limited weight parts as described above.

싸이클로펜탄은, 상기 A액과 B액의 분사 및 도포시 탄화를 방지하고 셀프레벨링을 가능하게 하는 물질로서, 상기 아이오도벤젠 100 중량부를 기준으로 30-40 중량부가 혼합되는데, 상기 중량부 보다 적게 혼합되면 탄화방지성이 저하되어 오히려 부분 균열이 더 발생되어 내구성이 저하되고, 상기 중량부 보다 많이 혼합되면 탄화방지성과 평탄성이 증대되어 부분 균열시 오히려 평탄성이 저하되는 문제점이 있으므로, 상기와 같은 한정된 중량부를 가지는 것이 바람직하다.Cyclopentane is a material that prevents carbonization and enables self-leveling when spraying and applying the A and B solutions, and is mixed in 30-40 parts by weight based on 100 parts by weight of the iodobenzene, less than the above parts by weight. When mixed, the anti-carbonization property is lowered and partial cracks are rather generated, resulting in lower durability, and when mixed more than the above weight part, carbonization prevention properties and flatness are increased, and there is a problem in that flatness is rather reduced during partial cracking. It is preferable to have parts by weight.

디에틸에테르는, 상기 A액과 B액의 분사 및 도포시 가사 시간을 조절하는 물질로서, 상기 아이오도벤젠 100 중량부를 기준으로 10-20 중량부가 혼합되는데, 상기 중량부 보다 적게 혼합되면 경화 시간이 너무 길어져 작업 시간이 증가되고, 상기 중량부 보다 많이 혼합되면 경화제인 B액의 점도가 너무 높아 분사 및 도포 작업이 불가능해지는 문제점이 있으므로, 상기와 같은 한정된 중량부를 가지는 것이 바람직하다.Diethyl ether is a substance that controls the pot life when spraying and applying the liquid A and the liquid B, and 10-20 parts by weight is mixed based on 100 parts by weight of the iodobenzene. This is too long, the working time is increased, and when mixed more than the above weight parts, there is a problem that the viscosity of the curing agent B solution is too high, so that spraying and coating operations are impossible, it is preferable to have a limited weight part as described above.

한편, 주제인 A액과 경화제인 B액은 5:5 내지 7:3의 부피비로 혼합되도록 하고 있는데, 상기 A액과 B액의 부피비율이 상기 범위를 벗어나는 경우 경화시간 조절 및 무게평균분자량의 조절에 어려움이 발생되어 경화불량, 들뜸 및 물성 저하로 인하여 균열이 많이 발생하고 작업성이 저하되는 문제점이 있으므로, 상기와 같은 한정된 범위의 부피비율로 혼합되는 것이 바람직하다.On the other hand, the main agent solution A and the curing agent solution B are mixed in a volume ratio of 5:5 to 7:3. If the volume ratio of the solution A and the solution B is out of the above range, the curing time is adjusted and the weight average molecular weight It is preferable to mix in a volume ratio in the limited range as described above, because there are problems in that there are problems in that there are many cracks and deterioration of workability due to poor curing, lifting, and deterioration of physical properties due to difficulty in control.

이하, 본 발명의 바람직한 실시예에 따른 폴리우레아를 이용한 균열보수제의 효과를 구체적인 실시예를 통해 설명하기로 한다. Hereinafter, the effect of the crack repair agent using polyurea according to a preferred embodiment of the present invention will be described with reference to specific examples.

이소시아누레이트 100 중량부에 쇼듐락테이트메틸실란올 60 중량부, 1,5-나프탈렌디이소시아네이트 50 중량부, 메틸비닐에테르 40 중량부, 알루미늄클로라이드 30 중량부 및 폴리옥시에틸렌리놀레이트 10 중량부가 혼합되고 80℃의 온도에서 승온된 후 5시간 반응되어 폴리우레아 A액이 제조되고, 아이오도벤젠 100 중량부에 페닐하이드라진 70 중량부, 세틸알콜에틸렌프로필렌코폴리머 60 중량부, 싸이클로펜탄 50 중량부 및 디에틸에테르 30 중량부가 혼합되어 경화제 B액이 제조된 후, 상기 A액과 B액이 5:5의 부피비로 혼합되어 폴리우레아를 이용한 균열보수제가 제조된다.To 100 parts by weight of isocyanurate, 60 parts by weight of shodium lactate methylsilanol, 50 parts by weight of 1,5-naphthalene diisocyanate, 40 parts by weight of methyl vinyl ether, 30 parts by weight of aluminum chloride and 10 parts by weight of polyoxyethylene linoleate After mixing and heating at a temperature of 80° C., the mixture was reacted for 5 hours to prepare a polyurea solution A, and 100 parts by weight of iodobenzene, 70 parts by weight of phenylhydrazine, 60 parts by weight of cetyl alcohol ethylene propylene copolymer, 50 parts by weight of cyclopentane and 30 parts by weight of diethyl ether to prepare a curing agent solution B, and then the solution A and solution B are mixed in a volume ratio of 5:5 to prepare a crack repair agent using polyurea.

이소시아누레이트 100 중량부에 쇼듐락테이트메틸실란올 75 중량부, 1,5-나프탈렌디이소시아네이트 65 중량부, 메틸비닐에테르 55 중량부, 알루미늄클로라이드 45 중량부 및 폴리옥시에틸렌리놀레이트 25 중량부가 혼합되고 100℃의 온도에서 승온된 후 6시간 반응되어 폴리우레아 A액이 제조되고, 아이오도벤젠 100 중량부에 페닐하이드라진 55 중량부, 세틸알콜에틸렌프로필렌코폴리머 45 중량부, 싸이클로펜탄 35 중량부 및 디에틸에테르 15 중량부가 혼합되어 경화제 B액이 제조된 후, 상기 A액과 B액이 5:5의 부피비로 혼합되어 제조된다.To 100 parts by weight of isocyanurate, 75 parts by weight of shodium lactate methylsilanol, 65 parts by weight of 1,5-naphthalene diisocyanate, 55 parts by weight of methyl vinyl ether, 45 parts by weight of aluminum chloride and 25 parts by weight of polyoxyethylene linoleate After mixing and raising the temperature at 100° C., the mixture was reacted for 6 hours to prepare a polyurea solution A, 55 parts by weight of phenylhydrazine, 45 parts by weight of cetyl alcohol ethylene propylene copolymer, 35 parts by weight of cyclopentane to 100 parts by weight of iodobenzene And 15 parts by weight of diethyl ether is mixed to prepare a curing agent solution B, and then the solution A and solution B are mixed in a volume ratio of 5:5.

이소시아누레이트 100 중량부에 쇼듐락테이트메틸실란올 90 중량부, 1,5-나프탈렌디이소시아네이트 80 중량부, 메틸비닐에테르 70 중량부, 알루미늄클로라이드 60 중량부 및 폴리옥시에틸렌리놀레이트 40 중량부가 혼합되고 120℃의 온도에서 승온된 후 7시간 반응되어 폴리우레아 A액이 제조되고, 아이오도벤젠 100 중량부에 페닐하이드라진 40 중량부, 세틸알콜에틸렌프로필렌코폴리머 30 중량부, 싸이클로펜탄 20 중량부 및 디에틸에테르 5 중량부가 혼합되어 경화제 B액이 제조된 후, 상기 A액과 B액이 5:5의 부피비로 혼합되어 제조된다.To 100 parts by weight of isocyanurate, 90 parts by weight of shodium lactate methylsilanol, 80 parts by weight of 1,5-naphthalene diisocyanate, 70 parts by weight of methyl vinyl ether, 60 parts by weight of aluminum chloride and 40 parts by weight of polyoxyethylene linoleate After mixing and heating at a temperature of 120° C., the mixture was reacted for 7 hours to prepare a polyurea solution A, and 100 parts by weight of iodobenzene, 40 parts by weight of phenylhydrazine, 30 parts by weight of cetyl alcohol ethylene propylene copolymer, 20 parts by weight of cyclopentane And 5 parts by weight of diethyl ether is mixed to prepare a curing agent solution B, and then the solution A and solution B are mixed in a volume ratio of 5:5.

한편, 상기 각각의 실시예의 폴리우레아를 이용한 균열보수제의 성능을 평가하기 위하여, KSF 4922, KSD 9502 및 KSF 4936 등에 의거하여, 시험편을 상기와 같이 제조한 다음 시제품 A사 및 B사와 비교하여 물성을 측정하였으며, 그 결과를 하기 표 1에 나타내었다. On the other hand, in order to evaluate the performance of the crack repair agent using polyurea of each of the above examples, according to KSF 4922, KSD 9502 and KSF 4936, the test pieces were prepared as described above, and then the physical properties were compared with the prototypes A and B. was measured, and the results are shown in Table 1 below.

Figure 112020143641117-pat00001
Figure 112020143641117-pat00001

따라서 본 발명의 바람직한 실시예에 따른 폴리우레아를 이용한 균열보수제는, 상기 표 1에 나타낸 바와 같이, 분자 구조 내에 강도 및 강인성이 부여되고 방수, 방식, 바닥재 등의 다양한 용도로 사용될 수 있고, 또한 주제와 경화제를 스프레이 장비로 시공을 하면 기존의 균열보수제에 비하여 내균열성이 우수하여 물성 저하가 발생하지 않도록 할 수 있다.Therefore, as shown in Table 1 above, the crack repair agent using polyurea according to a preferred embodiment of the present invention is given strength and toughness in the molecular structure and can be used for various purposes such as waterproofing, anticorrosion, flooring, and the like. If the curing agent is applied with spray equipment, the crack resistance is superior to that of the existing crack repair agent, so that the deterioration of the physical properties can be prevented.

한편, 본 발명의 바람직한 실시예에 따른 폴리우레아를 이용한 균열보수제를 이용한 도장(또는 보수), 방수 및 방식 공법은 다음과 같다.On the other hand, the coating (or repair), waterproofing and anticorrosion method using a crack repair agent using polyurea according to a preferred embodiment of the present invention is as follows.

먼저, 작업자에 의해 상기와 같이 조성되는 폴리우레아를 이용한 균열보수제가 시공되기 위한 콘크리트 표면이 청소 및 처리된다.First, the surface of the concrete for construction of the crack repair agent using the polyurea composition as described above is cleaned and treated by the worker.

여기서, 콘크리트 표면의 청소는, 콘크리트 표면에 붙어 있는 먼지, 오염물, 또는 오일을 제거하고 시공될 표면의 돌출부가 매끄럽게 처리되는 것을 포함한다.Here, the cleaning of the concrete surface includes removing dust, contaminants, or oil adhering to the concrete surface and smoothing the protrusion of the surface to be constructed.

이후, 본 발명의 바람직한 실시예에 따른 폴리우레아를 이용한 균열보수제가 제조된다.Thereafter, a crack repair agent using polyurea according to a preferred embodiment of the present invention is prepared.

이후, 도포 또는 분사수단에 의해 상기 표면 처리된 시공표면에 소정의 두께로 상기 폴리우레아를 이용한 균열보수제가 도포 또는 분사된 후 건조되어 소정 두께의 도막 형성을 통하여 도장, 방수 및 방식 공법이 완료된다.After that, the crack repair agent using the polyurea is applied or sprayed to a predetermined thickness on the surface-treated construction surface by an application or spraying means, and then dried and the coating, waterproofing and anticorrosion method is completed through the formation of a coating film of a predetermined thickness. .

따라서 본 발명에 의하면, 분자 구조 내에 강도 및 강인성이 부여되고 방수, 방식, 바닥재 등의 다양한 용도로 사용될 수 있고, 또한 주제와 경화제를 스프레이 장비로 시공을 하면 기존의 균열보수제에 비하여 내균열성이 우수하여 물성 저하가 발생하지 않도록 하여 우수한 도장, 방수 및 방식 공법을 제공할 수 있다.Therefore, according to the present invention, strength and toughness are imparted to the molecular structure, and it can be used for various purposes such as waterproofing, anti-corrosion, and flooring. Also, when the main agent and hardener are sprayed with a spray device, crack resistance is better than that of conventional crack repair agents. Excellent coating, waterproofing and anticorrosive method can be provided by preventing deterioration of physical properties.

이상 첨부된 도면을 참조하여 본 발명의 바람직한 실시예를 설명하였지만, 본 발명이 속하는 기술 분야에서 통상의 지식을 가진 자는 본 발명의 기술적 사상이나 필수적인 특징을 벗어나지 않는 범위 내에서 여러 가지로 치환, 변형 및 변경이 가능하므로 다른 구체적인 형태로 실시될 수 있다는 것을 이해할 수 있을 것이다. 그러므로 이상에서 기술한 실시예들은 모든 면에서 예시적인 것이며 한정적이 아닌 것으로 이해해야만 한다.Although preferred embodiments of the present invention have been described with reference to the accompanying drawings, those of ordinary skill in the art to which the present invention pertains may substitute variously within the scope without departing from the technical spirit or essential features of the present invention. and variations are possible, so it will be understood that the embodiments may be implemented in other specific forms. Therefore, it should be understood that the embodiments described above are illustrative in all respects and not restrictive.

Claims (5)

이소시아누레이트에 쇼듐락테이트메틸실란올, 1,5-나프탈렌디이소시아네이트, 메틸비닐에테르, 알루미늄클로라이드 및 폴리옥시에틸렌리놀레이트가 혼합되어 제조되는 폴리우레아 A액과;
아이오도벤젠에 페닐하이드라진, 세틸알콜에틸렌프로필렌코폴리머, 싸이클로펜탄 및 디에틸에테르가 혼합되어 제조되는 경화제 B액을 포함하는 것을 특징으로 하는 폴리우레아를 이용한 균열보수제.
a polyurea solution A prepared by mixing isocyanurate with shodium lactate methylsilanol, 1,5-naphthalene diisocyanate, methyl vinyl ether, aluminum chloride and polyoxyethylene linoleate;
A crack repair agent using polyurea, characterized in that it contains a curing agent B solution prepared by mixing iodobenzene with phenylhydrazine, cetyl alcohol ethylene propylene copolymer, cyclopentane and diethyl ether.
제1항에 있어서, A액은,
이소시아누레이트 100 중량부에 쇼듐락테이트메틸실란올 70-80 중량부, 1,5-나프탈렌디이소시아네이트 60-70 중량부, 메틸비닐에테르 50-60 중량부, 알루미늄클로라이드 40-50 중량부 및 폴리옥시에틸렌리놀레이트 20-30 중량부가 혼합되고 80℃-120℃의 온도에서 승온된 후 5-7시간 반응되어 제조되는 것을 특징으로 하는 폴리우레아를 이용한 균열보수제.
According to claim 1, Liquid A,
70-80 parts by weight of shodium lactate methylsilanol, 60-70 parts by weight of 1,5-naphthalene diisocyanate, 50-60 parts by weight of methyl vinyl ether, 40-50 parts by weight of aluminum chloride and A crack repair agent using polyurea, characterized in that it is prepared by mixing 20-30 parts by weight of polyoxyethylene linoleate, raising the temperature at a temperature of 80°C-120°C, and reacting for 5-7 hours.
제2항에 있어서, B액은,
아이오도벤젠 100 중량부에 페닐하이드라진 50-60 중량부, 세틸알콜에틸렌프로필렌코폴리머 40-50 중량부, 싸이클로펜탄 30-40 중량부 및 디에틸에테르 10-20 중량부가 혼합되어 제조되는 것을 특징으로 하는 폴리우레아를 이용한 균열보수제.
According to claim 2, Liquid B,
It is characterized in that 50-60 parts by weight of phenylhydrazine, 40-50 parts by weight of cetyl alcohol ethylene propylene copolymer, 30-40 parts by weight of cyclopentane and 10-20 parts by weight of diethyl ether are mixed in 100 parts by weight of iodobenzene. Crack repair agent using polyurea.
제3항에 있어서, A액과 B액은,
5:5 내지 7:3의 부피비로 혼합되어 제조되는 것을 특징으로 하는 폴리우레아를 이용한 균열보수제.
According to claim 3, A solution and B solution,
A crack repair agent using polyurea, characterized in that it is prepared by mixing in a volume ratio of 5:5 to 7:3.
시공 표면이 전처리되는 단계와;
제1항 내지 제4항 중 어느 한 항에 따른 폴리우레아를 이용한 균열보수제가 제조되는 단계와;
도포 또는 분사수단에 의해 상기 시공 표면에 소정의 두께로 폴리우레아를 이용한 균열제가 도포 또는 분사되는 단계를 포함하는 것을 특징으로 하는 폴리우레아를 이용한 균열보수제를 이용한 도장, 방수 및 방식 공법.
pretreatment of the construction surface;
5. A method comprising: preparing a crack repair agent using the polyurea according to any one of claims 1 to 4;
A coating, waterproofing and anticorrosive construction method using a crack repair agent using polyurea, comprising the step of applying or spraying a cracking agent using polyurea to a predetermined thickness on the construction surface by an application or spraying means.
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Publication number Priority date Publication date Assignee Title
KR20020063284A (en) * 2000-10-30 2002-08-01 미쯔이가가꾸가부시끼가이샤 Organic Polymer and Novel Polymerizable Compound
JP2010047762A (en) * 2008-08-20 2010-03-04 E I Du Pont De Nemours & Co Method for producing polyurethane urea resin dispersion
KR101163801B1 (en) * 2004-04-14 2012-07-09 바스프 에스이 Radiation curable 1,3,5-triazine carbamates and 1,3,5-triazine ureas containing vinyl groups, methacryloyl groups, or acryloyl groups
KR101832433B1 (en) * 2017-12-13 2018-02-26 주식회사 성오방수건설 Polyurea waterproof agent with high heat exchanging function and manufacturing method thereof and waterproof method using thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20020063284A (en) * 2000-10-30 2002-08-01 미쯔이가가꾸가부시끼가이샤 Organic Polymer and Novel Polymerizable Compound
KR101163801B1 (en) * 2004-04-14 2012-07-09 바스프 에스이 Radiation curable 1,3,5-triazine carbamates and 1,3,5-triazine ureas containing vinyl groups, methacryloyl groups, or acryloyl groups
JP2010047762A (en) * 2008-08-20 2010-03-04 E I Du Pont De Nemours & Co Method for producing polyurethane urea resin dispersion
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