KR20220075886A - Solvent-free type water soluble epoxy flooring - Google Patents

Solvent-free type water soluble epoxy flooring Download PDF

Info

Publication number
KR20220075886A
KR20220075886A KR1020200164476A KR20200164476A KR20220075886A KR 20220075886 A KR20220075886 A KR 20220075886A KR 1020200164476 A KR1020200164476 A KR 1020200164476A KR 20200164476 A KR20200164476 A KR 20200164476A KR 20220075886 A KR20220075886 A KR 20220075886A
Authority
KR
South Korea
Prior art keywords
calcium carbonate
solvent
bisphenol
soluble epoxy
diglycidyl ether
Prior art date
Application number
KR1020200164476A
Other languages
Korean (ko)
Other versions
KR102476926B1 (en
Inventor
임종일
정우선
Original Assignee
주식회사 제일화성
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 주식회사 제일화성 filed Critical 주식회사 제일화성
Priority to KR1020200164476A priority Critical patent/KR102476926B1/en
Publication of KR20220075886A publication Critical patent/KR20220075886A/en
Application granted granted Critical
Publication of KR102476926B1 publication Critical patent/KR102476926B1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/20Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
    • C08G59/22Di-epoxy compounds
    • C08G59/226Mixtures of di-epoxy compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/4007Curing agents not provided for by the groups C08G59/42 - C08G59/66
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/50Amines
    • C08G59/504Amines containing an atom other than nitrogen belonging to the amine group, carbon and hydrogen

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Epoxy Resins (AREA)

Abstract

경화 시 기계적 강도가 우수하고, 부착성, 침투성, 내마모성, 내수성, 내약품성이 우수하며, 저장성 및 침전 방지성이 우수한 무용제형 수용성 에폭시 바닥재에 대하여 개시한다.
본 발명에 따른 무용제형 수용성 에폭시 바닥재는 주제; 및 경화제;를 포함하며, 상기 주제는 비스페놀 A 다이글리시딜 에테르, 1,4-부탄디올디글리시딜 에테르를 포함하고, 상기 경화제는 탄산칼슘, 폴리(옥시프로필렌)디아민, 비스페놀 A-비스페놀 A 디글리시딜 에테르 중합체를 포함한다.
Disclosed is a solvent-free, water-soluble epoxy flooring material having excellent mechanical strength during curing, excellent adhesion, permeability, abrasion resistance, water resistance and chemical resistance, and excellent storage and precipitation prevention properties.
Solvent-free water-soluble epoxy flooring according to the present invention is the main subject; and a curing agent; wherein the subject includes bisphenol A diglycidyl ether, 1,4-butanediol diglycidyl ether, and the curing agent includes calcium carbonate, poly(oxypropylene)diamine, bisphenol A-bisphenol A diglycidyl ether polymers.

Description

무용제형 수용성 에폭시 바닥재{SOLVENT-FREE TYPE WATER SOLUBLE EPOXY FLOORING}Solvent-free water-soluble epoxy flooring {SOLVENT-FREE TYPE WATER SOLUBLE EPOXY FLOORING}

본 발명은 무용제형 수용성 에폭시 바닥재에 관한 것이다. The present invention relates to a solvent-free water-soluble epoxy flooring.

일반적으로 건물의 바닥에는 분진 방지 기능, 내마모성, 내구성, 난연성 등을 고려하여 적절한 바닥재 선정이 이루어진다. 이러한 바닥 마감 공법으로서, 종래 에폭시 및 우레탄 코팅, 무용제 에폭시나 우레탄과 에폭시 레진 몰탈 등 다양한 소재의 제품이 사용되고 있다.In general, for the floor of a building, an appropriate flooring material is selected in consideration of the dust prevention function, abrasion resistance, durability, and flame retardancy. As such a floor finishing method, conventional epoxy and urethane coatings, solvent-free epoxy, urethane and epoxy resin mortar, etc. are used.

이와 관련하여, 시멘트계 아크릴 무기질 바닥재와 시멘트계 우레탄 무기질 바닥재 등이 개발되어 사용되고 있다.In this regard, cement-based acrylic inorganic flooring materials and cement-based urethane inorganic flooring materials have been developed and used.

하지만, 무기질 바닥재 외에 보편적으로 사용되는 유기계 도료는, 화재에 매우 취약하며, 화재 시 유독 가스를 방출하는 등 점차 사용이 제한되고 있는 실정이다.However, organic paints that are commonly used in addition to inorganic flooring materials are very vulnerable to fire, and their use is gradually restricted, such as emitting toxic gas in case of fire.

또한 상기 종래 기술들은 모두 VOCs(휘발성유기화합물)을 함유하는 유성제품으로서 시공 시 작업성 향상을 위해 희석제(Thinner)를 적게는 2~3%에서 많게는 30~40%까지 희석해서 사용해야 하며, 이는 인체에 유해함은 물론 환경파괴의 원인이 되고 있다.In addition, all of the above prior arts are oil-based products containing VOCs (volatile organic compounds), and in order to improve workability during construction, a thinner should be used after diluting from 2-3% to 30-40% as much as possible. It is not only harmful to the environment, but also causes environmental damage.

한편, 최근에 각광받고 있는 무기질 바닥재는 기존의 유기계 도료의 문제점을 보완하여, 환경 친화적인 제품으로 인정받고 있으나, 제품의 기준이 아직 정립이 않되 있어, 품질이 불안정하다. 또한 필요 이상의 과도한 자재 사용으로, 가격이 비싸며, 시공이 까다로워 전문 시공 인력이 필요하다.On the other hand, inorganic flooring materials, which have recently been spotlighted, are recognized as environmentally friendly products by supplementing the problems of existing organic paints, but the product standards have not yet been established, so the quality is unstable. In addition, the use of excessive materials more than necessary, the price is high, and the construction is difficult, so professional construction personnel are required.

본 발명의 목적은 경화 시 기계적 강도가 우수하고, 부착성, 침투성, 내마모성, 내수성, 내약품성이 우수한 무용제형 수용성 에폭시 바닥재를 제공하는 것이다.An object of the present invention is to provide a solvent-free water-soluble epoxy flooring material having excellent mechanical strength upon curing, and excellent adhesion, permeability, abrasion resistance, water resistance and chemical resistance.

또한 본 발명의 목적은 친환경적이며, 내먼지성, 저장성 및 침전 방지성이 우수한 무용제형 수용성 에폭시 바닥재를 제공하는 것이다. It is also an object of the present invention to provide a solvent-free water-soluble epoxy flooring material that is environmentally friendly and has excellent dust resistance, storability and precipitation prevention properties.

본 발명의 목적들은 이상에서 언급한 목적으로 제한되지 않으며, 언급되지 않은 본 발명의 다른 목적 및 장점들은 하기의 설명에 의해서 이해될 수 있고, 본 발명의 실시예에 의해 보다 분명하게 이해될 것이다. 또한, 본 발명의 목적 및 장점들은 특허 청구 범위에 나타낸 수단 및 그 조합에 의해 실현될 수 있음을 쉽게 알 수 있을 것이다.The objects of the present invention are not limited to the above-mentioned objects, and other objects and advantages of the present invention not mentioned can be understood by the following description, and will be more clearly understood by the examples of the present invention. It will also be readily apparent that the objects and advantages of the present invention may be realized by the means and combinations thereof indicated in the appended claims.

본 발명에 따른 무용제형 수용성 에폭시 바닥재는 주제; 및 경화제;를 포함하며, 상기 주제는 비스페놀 A 다이글리시딜 에테르, 1,4-부탄디올디글리시딜 에테르를 포함하고, 상기 경화제는 탄산칼슘, 폴리(옥시프로필렌)디아민, 비스페놀 A-비스페놀 A 디글리시딜 에테르 중합체를 포함한다.Solvent-free water-soluble epoxy flooring according to the present invention is the main subject; and a curing agent; wherein the subject includes bisphenol A diglycidyl ether, 1,4-butanediol diglycidyl ether, and the curing agent includes calcium carbonate, poly(oxypropylene)diamine, bisphenol A-bisphenol A diglycidyl ether polymers.

본 발명에 따른 무용제형 수용성 에폭시 바닥재는 경화 시 기계적 강도가 우수하고, 부착성, 침투성, 내마모성, 내수성, 내약품성이 우수하며, 광택이 우수하여 표면이 미려하다.The solvent-free water-soluble epoxy flooring material according to the present invention has excellent mechanical strength when cured, has excellent adhesion, permeability, abrasion resistance, water resistance, and chemical resistance, and has a beautiful surface due to excellent gloss.

또한 상기 무용제형 수용성 에폭시 바닥재는 밀폐된 공간에서도 작업이 용이하며 친환경적이다.In addition, the solvent-free water-soluble epoxy flooring is easy to work in a closed space and is environmentally friendly.

또한 상기 무용제형 수용성 에폭시 바닥재는 내먼지성이 우수하다.In addition, the solvent-free water-soluble epoxy flooring material has excellent dust resistance.

또한 상기 무용제형 수용성 에폭시 바닥재는 저장성 및 침전 방지성이 우수하다. In addition, the solvent-free water-soluble epoxy flooring material has excellent storage properties and precipitation prevention properties.

상술한 효과와 더불어 본 발명의 구체적인 효과는 이하 발명을 실시하기 위한 구체적인 사항을 설명하면서 함께 기술한다.In addition to the above-described effects, the specific effects of the present invention will be described together while describing specific details for carrying out the invention below.

전술한 목적, 특징 및 장점은 첨부된 도면을 참조하여 상세하게 후술되며, 이에 따라 본 발명이 속하는 기술분야에서 통상의 지식을 가진 자가 본 발명의 기술적 사상을 용이하게 실시할 수 있을 것이다. 본 발명을 설명함에 있어서 본 발명과 관련된 공지 기술에 대한 구체적인 설명이 본 발명의 요지를 불필요하게 흐릴 수 있다고 판단되는 경우에는 상세한 설명을 생략한다. 이하, 첨부된 도면을 참조하여 본 발명에 따른 바람직한 실시예를 상세히 설명하기로 한다. 도면에서 동일한 참조부호는 동일 또는 유사한 구성요소를 가리키는 것으로 사용된다.The above-described objects, features and advantages will be described below in detail with reference to the accompanying drawings, and accordingly, those of ordinary skill in the art to which the present invention pertains will be able to easily implement the technical idea of the present invention. In describing the present invention, if it is determined that a detailed description of a known technology related to the present invention may unnecessarily obscure the gist of the present invention, the detailed description will be omitted. Hereinafter, preferred embodiments according to the present invention will be described in detail with reference to the accompanying drawings. In the drawings, the same reference numerals are used to indicate the same or similar components.

또한 어떤 구성요소가 다른 구성요소에 "연결", "결합" 또는 "접속"된다고 기재된 경우, 상기 구성요소들은 서로 직접적으로 연결되거나 또는 접속될 수 있지만, 각 구성요소 사이에 다른 구성요소가 "개재"되거나, 각 구성요소가 다른 구성요소를 통해 "연결", "결합" 또는 "접속"될 수도 있는 것으로 이해되어야 할 것이다. Also, when it is described that a component is "connected", "coupled" or "connected" to another component, the components may be directly connected or connected to each other, but other components are "interposed" between each component. It should be understood that “or, each component may be “connected,” “coupled,” or “connected,” through another component.

이하에서는, 본 발명의 몇몇 실시예에 따른 무용제형 수용성 에폭시 바닥재를 설명하도록 한다.Hereinafter, a solvent-free water-soluble epoxy flooring according to some embodiments of the present invention will be described.

본 발명의 무용제형 수용성 에폭시 바닥재는 우수한 기계적 특성과 함께 내마모성, 내약품성, 미려한 표면이 요구되는 바닥재로, 일반공장, 물류창고, 지하주차장, 병원, 원자력발전소, 실험실, 일반사무실, 복도 등의 바닥재로 사용될 수 있다.The solvent-free water-soluble epoxy flooring material of the present invention is a flooring material that requires excellent mechanical properties as well as abrasion resistance, chemical resistance, and a beautiful surface. can be used as

본 발명의 무용제형 수용성 에폭시 바닥재는 주제 및 경화제를 포함한다.The solvent-free water-soluble epoxy flooring of the present invention includes a main agent and a curing agent.

상기 주제는 비스페놀 A 다이글리시딜 에테르, 1,4-부탄디올디글리시딜 에테르를 포함한다.The subject includes bisphenol A diglycidyl ether, 1,4-butanediol diglycidyl ether.

비스페놀 A 다이글리시딜 에테르는 주제의 주성분이며, 물성에 주요한 영향을 미친다. 비스페놀 A 다이글리시딜 에테르는 2,2''-((1-METHYLETHYLIDENE)BIS(4,1-PHENYLENEOXYMETHYLENE))BIS-OXIRANE 이라고도 불리우며, CAS 번호는 1675-54-3이다. Bisphenol A diglycidyl ether is the main component of the subject and has a major influence on physical properties. Bisphenol A diglycidyl ether is also called 2,2''-((1-METHYLETHYLIDENE)BIS(4,1-PHENYLENEOXYMETHYLENE))BIS-OXIRANE, CAS number 1675-54-3.

1,4-부탄디올디글리시딜 에테르는 2,2'-(1,4-부탄디일비스(옥시메틸렌))비스-옥시란 이라고도 불리우며, CAS 번호는 2425-79-8이다. 1,4-Butanedioldiglycidyl ether is also called 2,2'-(1,4-butanediylbis(oxymethylene))bis-oxirane, CAS number 2425-79-8.

상기 주제는 비스페놀 A 다이글리시딜 에테르 100중량부에 대하여, 1,4-부탄디올디글리시딜 에테르 20~40중량부를 포함한다. The subject includes 20 to 40 parts by weight of 1,4-butanediol diglycidyl ether based on 100 parts by weight of bisphenol A diglycidyl ether.

1,4-부탄디올디글리시딜 에테르의 함량이 20~40중량부를 벗어나는 경우, 경화 시, 요구하는 물성을 나타내기 어려울 수 있다.When the content of 1,4-butanediol diglycidyl ether is out of 20 to 40 parts by weight, it may be difficult to exhibit required physical properties during curing.

상기 경화제는 탄산칼슘, 폴리(옥시프로필렌)디아민, 비스페놀 A-비스페놀 A 디글리시딜 에테르 중합체를 포함한다.The curing agent includes calcium carbonate, poly(oxypropylene)diamine, and bisphenol A-bisphenol A diglycidyl ether polymer.

탄산칼슘은 에폭시 바닥재의 침전 방지를 위해 경화제에 투입되는 것이 바람직하다.Calcium carbonate is preferably added to the curing agent to prevent precipitation of the epoxy flooring material.

구체적으로, 탄산칼슘은 저장성 및 침전 방지를 위해 서로 다른 직경을 갖는 탄산칼슘을 포함한다.Specifically, calcium carbonate includes calcium carbonate having different diameters for storage stability and prevention of precipitation.

상기 탄산칼슘은 D1의 직경을 갖는 제1탄산칼슘, D2의 직경을 갖는 제2탄산칼슘, D3의 직경을 갖는 제3탄산칼슘을 포함한다. The calcium carbonate includes primary calcium carbonate having a diameter of D1, secondary calcium carbonate having a diameter of D2, and tertiary calcium carbonate having a diameter of D3.

이 경우, 직경을 비교해보면 D1〈 D2〈 D3 일 수 있다.In this case, if the diameter is compared, it may be D1 < D2 < D3.

예를 들어, D1 은 0.1~3㎛ 이고, D2는 4~8㎛, D3은 9~15㎛ 일 수 있다.For example, D1 may be 0.1 to 3 μm, D2 may be 4 to 8 μm, and D3 may be 9 to 15 μm.

상기 제1탄산칼슘의 함량이 A, 제2탄산칼슘의 함량이 B, 제3탄산칼슘의 함량이 C라고 할 때, A 〈 B〈 C 일 수 있다.When the content of the first calcium carbonate is A, the content of the second calcium carbonate is B, and the content of the third calcium carbonate is C, A < B < C.

예를 들어, 탄산칼슘은 제3탄산칼슘 100중량부에 대하여, 제2탄산칼슘은 20~50중량부, 제1탄산칼슘은 0.1~10중량부를 포함할 수 있다.For example, calcium carbonate may contain 20 to 50 parts by weight of calcium carbonate, 0.1 to 10 parts by weight of calcium carbonate, and 0.1 to 10 parts by weight of calcium carbonate, based on 100 parts by weight of calcium tertiary.

제1탄산칼슘, 제2탄산칼슘, 제3탄산칼슘의 상기 함량을 만족함에 따라 경화성 및 내수성 뿐만 아니라 기계적 강도를 확보하기에 유리할 수 있다.As the content of the first calcium carbonate, the second calcium carbonate, and the third calcium carbonate is satisfied, it may be advantageous to secure mechanical strength as well as hardenability and water resistance.

폴리(옥시프로필렌)디아민은 CAS 번호 9046-10-0이다.Poly(oxypropylene)diamine is CAS number 9046-10-0.

비스페놀 A-비스페놀 A 디글리시딜 에테르 중합체는 CAS 번호 25036-25-3이다.The bisphenol A-bisphenol A diglycidyl ether polymer is CAS number 25036-25-3.

상기 경화제는 탄산칼슘 100중량부에 대하여, 폴리(옥시프로필렌)디아민 15~40중량부, 비스페놀 A-비스페놀 A 디글리시딜 에테르 중합체 1~15중량부를 포함한다.The curing agent includes 15 to 40 parts by weight of poly(oxypropylene)diamine and 1 to 15 parts by weight of bisphenol A-bisphenol A diglycidyl ether polymer based on 100 parts by weight of calcium carbonate.

폴리(옥시프로필렌)디아민과 비스페놀 A-비스페놀 A 디글리시딜 에테르 중합체의 함량이 상기 범위를 벗어나는 경우, 경화 시 요구하는 물성을 나타내기 어려울 수 있다.When the content of poly(oxypropylene)diamine and bisphenol A-bisphenol A diglycidyl ether polymer is out of the above range, it may be difficult to exhibit physical properties required during curing.

상기 주제의 점도는 25℃에서 1000~1500cps 일 수 있고, 비중이 1.0~1.2일 수 있다.The viscosity of the subject may be 1000 ~ 1500 cps at 25 ℃, the specific gravity may be 1.0 ~ 1.2.

상기 경화제의 점도는 25℃에서 1500~3000cps 일 수 있고, 비중이 1.3~1.4일 수 있다.The viscosity of the curing agent may be 1500 ~ 3000cps at 25 ℃, specific gravity may be 1.3 ~ 1.4.

상기 경화제는 경화 촉진제로서 2,4,6-트리스(다이메틸아미노메틸)페놀을 더 포함할 수 있다. 상기 2,4,6-트리스(다이메틸아미노메틸)페놀은 경화제에 포함되어 경화시간을 조절한다.The curing agent may further include 2,4,6-tris(dimethylaminomethyl)phenol as a curing accelerator. The 2,4,6-tris(dimethylaminomethyl)phenol is included in the curing agent to control the curing time.

상기 경화제는 탄산칼슘 100중량부에 대하여, 2,4,6-트리스(다이메틸아미노메틸)페놀 0.1~15중량부를 더 포함할 수 있다.The curing agent may further include 0.1 to 15 parts by weight of 2,4,6-tris(dimethylaminomethyl)phenol based on 100 parts by weight of calcium carbonate.

상기 2,4,6-트리스(다이메틸아미노메틸)페놀의 함량이 0.1~15중량부를 벗어나는 경우, 경화시간 및 가사시간을 조절하기 어려워 작업성이 저하될 수 있다.When the content of the 2,4,6-tris(dimethylaminomethyl)phenol is out of 0.1 to 15 parts by weight, it is difficult to control the curing time and the pot life, and workability may be deteriorated.

추가로, 상기 경화제는 안료를 더 포함할 수 있다.Additionally, the curing agent may further include a pigment.

안료는 색상을 나타내기 위해 투입하는 원료라면 제한없이 사용될 수 있다.The pigment may be used without limitation as long as it is a raw material input to express color.

본 발명의 무용제형 수용성 에폭시 바닥재 수지 : 경화제는 1 : 0.8 ~ 1 : 1.2의 당량비로 포함된다. 이때 경화제는 탄산칼슘 필러가 포함되지 않은 경화제를 가리킨다.Solvent-free water-soluble epoxy flooring resin of the present invention: curing agent is included in an equivalent ratio of 1: 0.8 to 1: 1.2. In this case, the curing agent refers to a curing agent that does not contain a calcium carbonate filler.

그리고 상기 주제 : 경화제는 1 : 1 ~ 1 : 3의 중량비로 포함된다.And the subject: the curing agent is included in a weight ratio of 1:1 to 1:3.

경화제에 탄산칼슘이라는 필러가 포함되어 주제보다 경화제의 함량이 좀 더 클 수 있다. 경화제의 비율에 따라 바닥재 경화 시 물성이 변화할 수 있으며, 1 : 1 ~ 1 : 3 범위에서 우수한 물성을 확보할 수 있다.Since the curing agent contains a filler called calcium carbonate, the content of the curing agent may be larger than that of the main agent. Depending on the ratio of the curing agent, the physical properties may change during hardening of the flooring, and excellent physical properties may be secured in the range of 1:1 to 1:3.

본 발명에 따른 무용제형 수용성 에폭시 바닥재는 다음과 같이 제조될 수 있다.The solvent-free water-soluble epoxy flooring material according to the present invention can be prepared as follows.

먼저, 비스페놀 A 다이글리시딜 에테르, 1,4-부탄디올디글리시딜 에테르를 제시한 범위로 혼합하여 주제를 마련한다.First, bisphenol A diglycidyl ether and 1,4-butanediol diglycidyl ether are mixed in the indicated ranges to prepare a main ingredient.

그리고 탄산칼슘, 폴리(옥시프로필렌)디아민, 비스페놀 A-비스페놀 A 디글리시딜 에테르 중합체를 제시한 범위로 혼합하여 경화제를 마련한다.Then, calcium carbonate, poly(oxypropylene)diamine, and bisphenol A-bisphenol A diglycidyl ether polymer are mixed in the indicated ranges to prepare a curing agent.

마련된 주제와 경화제를 중량비로 혼합하여 무용제형 수용성 에폭시 바닥재를 제조할 수 있다.A solvent-free water-soluble epoxy flooring material can be prepared by mixing the prepared main material and a curing agent in a weight ratio.

상기 무용제형 수용성 에폭시 바닥재를 이용한 가사시간은 대략 10~60분일 수 있고, 지촉 건조시간은 4~5시간, 경화시간은 적어도 24시간 이상일 수 있다.Pot life using the solvent-free water-soluble epoxy flooring may be approximately 10 to 60 minutes, dry to touch time may be 4 to 5 hours, and curing time may be at least 24 hours or longer.

또한 무용제형 수용성 에폭시 바닥재의 경화물은 쇼어 경도 D 70이상을 나타낼 수 있다.In addition, the cured product of the solvent-free water-soluble epoxy flooring material may exhibit a shore hardness of D 70 or more.

이처럼, 본 발명에 따른 무용제형 수용성 에폭시 바닥재는 비스페놀 A 계열을 주성분으로 하는 주제에, 탄산칼슘을 주성분으로 하는 경화제를 당량비로 혼합함으로써, 경화 시 기계적 강도가 우수하고, 부착성, 침투성, 내마모성, 내수성, 내약품성이 우수한 효과가 있다.As such, the solvent-free water-soluble epoxy flooring material according to the present invention has excellent mechanical strength during curing by mixing a bisphenol A-based main component with a curing agent containing calcium carbonate as a main component in an equivalent ratio, adhesion, permeability, abrasion resistance, It has excellent water resistance and chemical resistance.

또한 무용제형 수용성 에폭시 바닥재는 친환경적이며, 내먼지성, 저장성 및 침전 방지성이 우수한 효과가 있다.In addition, solvent-free water-soluble epoxy flooring is eco-friendly and has excellent dust resistance, storability and precipitation prevention properties.

이와 같이 무용제형 수용성 에폭시 바닥재에 대하여 그 구체적인 실시예를 살펴보면 다음과 같다.As described above, a specific example of the solvent-free water-soluble epoxy flooring material will be described as follows.

1. 무용제형 수용성 에폭시 바닥재의 제조1. Preparation of solvent-free water-soluble epoxy flooring

실시예 1Example 1

비스페놀 A 다이글리시딜 에테르 100중량부에 대하여, 1,4-부탄디올디글리시딜 에테르 20중량부를 혼합하여 주제를 마련하였다.With respect to 100 parts by weight of bisphenol A diglycidyl ether, 20 parts by weight of 1,4-butanediol diglycidyl ether was mixed to prepare a main agent.

탄산칼슘 100중량부에 대하여, 폴리(옥시프로필렌)디아민 15중량부, 비스페놀 A-비스페놀 A 디글리시딜 에테르 중합체 5중량부를 혼합하여 경화제를 마련하였다.With respect to 100 parts by weight of calcium carbonate, 15 parts by weight of poly(oxypropylene)diamine and 5 parts by weight of bisphenol A-bisphenol A diglycidyl ether polymer were mixed to prepare a curing agent.

상기 탄산칼슘은 직경이 9~15㎛인 제3탄산칼슘 100중량부에 대하여, 직경이 0.1~3㎛인 제1탄산칼슘 5중량부, 직경이 4~8㎛인 제2탄산칼슘 20중량부를 포함하였다.The calcium carbonate is based on 100 parts by weight of tertiary calcium carbonate having a diameter of 9 to 15 μm, 5 parts by weight of first calcium carbonate having a diameter of 0.1 to 3 μm, and 20 parts by weight of second calcium carbonate having a diameter of 4 to 8 μm. included.

마련된 주제와 경화제를 1:2의 중량비로 혼합하여 무용제형 수용성 에폭시 바닥재를 제조하였다.A solvent-free water-soluble epoxy flooring was prepared by mixing the prepared main material and curing agent in a weight ratio of 1:2.

실시예 2Example 2

주제에서 1,4-부탄디올디글리시딜 에테르 40중량부를 혼합한 점을 제외하고는 실시예 1과 동일한 조건으로 무용제형 수용성 에폭시 바닥재를 제조하였다.A solvent-free water-soluble epoxy flooring material was prepared under the same conditions as in Example 1, except that 40 parts by weight of 1,4-butanediol diglycidyl ether was mixed in the subject matter.

실시예 3Example 3

경화제에서 폴리(옥시프로필렌)디아민 40중량부, 비스페놀 A-비스페놀 A 디글리시딜 에테르 중합체 15중량부를 혼합한 점을 제외하고는 실시예 1과 동일한 조건으로 무용제형 수용성 에폭시 바닥재를 제조하였다.A solvent-free water-soluble epoxy flooring was prepared under the same conditions as in Example 1, except that 40 parts by weight of poly(oxypropylene)diamine and 15 parts by weight of bisphenol A-bisphenol A diglycidyl ether polymer were mixed in the curing agent.

실시예 4Example 4

경화제에 탄산칼슘 100중량부에 대하여, 2,4,6-트리스(다이메틸아미노메틸)페놀 10중량부를 더 포함한 점을 제외하고는 실시예 1과 동일한 조건으로 무용제형 수용성 에폭시 바닥재를 제조하였다.A solvent-free water-soluble epoxy flooring was prepared under the same conditions as in Example 1, except that 10 parts by weight of 2,4,6-tris(dimethylaminomethyl)phenol was further included with respect to 100 parts by weight of calcium carbonate in the curing agent.

비교예 1Comparative Example 1

주제에서 1,4-부탄디올디글리시딜 에테르 50중량부를 혼합한 점을 제외하고는 실시예 1과 동일한 조건으로 무용제형 수용성 에폭시 바닥재를 제조하였다.A solvent-free water-soluble epoxy flooring material was prepared under the same conditions as in Example 1, except that 50 parts by weight of 1,4-butanediol diglycidyl ether was mixed in the subject matter.

비교예 2Comparative Example 2

경화제에서 폴리(옥시프로필렌)디아민 50중량부, 비스페놀 A-비스페놀 A 디글리시딜 에테르 중합체 20중량부를 혼합한 점을 제외하고는 실시예 1과 동일한 조건으로 무용제형 수용성 에폭시 바닥재를 제조하였다.A solvent-free water-soluble epoxy flooring was prepared under the same conditions as in Example 1, except that 50 parts by weight of poly(oxypropylene)diamine and 20 parts by weight of bisphenol A-bisphenol A diglycidyl ether polymer were mixed in the curing agent.

비교예 3Comparative Example 3

경화제에 직경이 9~15㎛인 탄산칼슘만을 포함한 점을 제외하고는 실시예 1과 동일한 조건으로 무용제형 수용성 에폭시 바닥재를 제조하였다.A solvent-free water-soluble epoxy flooring was prepared under the same conditions as in Example 1, except that only calcium carbonate having a diameter of 9 to 15 μm was included in the curing agent.

비교예 4Comparative Example 4

주제와 경화제를 1:0.5의 중량비로 혼합한 점을 제외하고는 실시예 1과 동일한 조건으로 무용제형 수용성 에폭시 바닥재를 제조하였다.A solvent-free water-soluble epoxy flooring was prepared under the same conditions as in Example 1, except that the main agent and the curing agent were mixed in a weight ratio of 1:0.5.

2. 물성 평가 방법 및 그 결과2. Methods for evaluating physical properties and their results

상기 실시예 1~4 및 비교예 1~4에서 제조된 무용제형 수용성 에폭시 바닥재를 이용하여 다음과 같이, 물성 평가를 실시하였다.Using the solvent-free water-soluble epoxy flooring prepared in Examples 1 to 4 and Comparative Examples 1 to 4, physical properties were evaluated as follows.

경도(Sh.D)는 KSM ISO 868에 의거하여 측정하였고, 압축강도(N/mm2), 굽힘강도(N/mm2), 충격강도(J/m), 인장강도(N/mm2) 는 KSM 3015에 의거하여 측정하였다.Hardness (Sh.D) was measured according to KSM ISO 868, compressive strength (N/mm 2 ), bending strength (N/mm 2 ), impact strength (J/m), tensile strength (N/mm 2 ) was measured according to KSM 3015.

[표 1][Table 1]

Figure pat00001
Figure pat00001

표 1을 참조하면, 본 발명에 따른 무용제형 수용성 에폭시 바닥재 실시예 1 내지 4의 경화물은 우수한 기계적 강도를 나타낸다.Referring to Table 1, the cured products of Examples 1 to 4 of the solvent-free water-soluble epoxy flooring according to the present invention exhibit excellent mechanical strength.

압축강도는 100~120N/mm2, 굽힘강도는 50~60N/mm2, 충격강도는 17~30 J/m, 인장강도는 36~50N/mm2을 보인다.Compressive strength is 100~120N/mm 2 , bending strength is 50~60N/mm 2 , impact strength is 17~30 J/m, and tensile strength is 36~50N/mm 2 .

실시예 1 내지 4는 기존 유성 바닥재에 비해 동등 이상의 물성을 나타내며, 휘발성 유기화합물을 발생시키지 않아 친환경 제품으로 사용될 수 있다.Examples 1 to 4 exhibit physical properties equal to or greater than those of conventional oil-based flooring materials, and do not generate volatile organic compounds, so they can be used as eco-friendly products.

따라서, 우수한 기계적 강도를 나타냄과 동시에 친환경적으로 사용되기 위해서는 비스페놀 A 다이글리시딜 에테르, 1,4-부탄디올디글리시딜 에테르를 포함하는 주제와, 탄산칼슘, 폴리(옥시프로필렌)디아민, 비스페놀 A-비스페놀 A 디글리시딜 에테르 중합체를 포함하는 경화제를 포함하는 것이 바람직하다.Therefore, in order to exhibit excellent mechanical strength and be environmentally friendly at the same time, a main agent containing bisphenol A diglycidyl ether and 1,4-butanediol diglycidyl ether, calcium carbonate, poly(oxypropylene)diamine, and bisphenol A - Preference is given to including a curing agent comprising a bisphenol A diglycidyl ether polymer.

이상과 같이 본 발명에 대해서 예시한 실시예를 참조로 하여 설명하였으나, 본 명세서에 개시된 실시예에 의해 본 발명이 한정되는 것은 아니며, 본 발명의 기술사상의 범위 내에서 통상의 기술자에 의해 다양한 변형이 이루어질 수 있음은 자명하다. 아울러 앞서 본 발명의 실시 예를 설명하면서 본 발명의 구성에 따른 작용 효과를 명시적으로 기재하여 설명하지 않았을 지라도, 해당 구성에 의해 예측 가능한 효과 또한 인정되어야 함은 당연하다.As described above, the present invention has been described with reference to the illustrated embodiments, but the present invention is not limited by the embodiments disclosed herein, and various modifications can be made by those skilled in the art within the scope of the technical spirit of the present invention. It is obvious that this can be done. In addition, although the effects according to the configuration of the present invention have not been explicitly described and described while describing the embodiments of the present invention, it is natural that the effects predictable by the configuration should also be recognized.

Claims (6)

주제; 및 경화제;를 포함하며,
상기 주제는
비스페놀 A 다이글리시딜 에테르, 1,4-부탄디올디글리시딜 에테르를 포함하고,
상기 경화제는 탄산칼슘, 폴리(옥시프로필렌)디아민, 비스페놀 A-비스페놀 A 디글리시딜 에테르 중합체를 포함하는 무용제형 수용성 에폭시 바닥재.
topic; and a curing agent; and
the subject is
bisphenol A diglycidyl ether, 1,4-butanediol diglycidyl ether;
The curing agent is a solvent-free water-soluble epoxy flooring material comprising calcium carbonate, poly (oxypropylene) diamine, bisphenol A-bisphenol A diglycidyl ether polymer.
제1항에 있어서,
상기 주제는 비스페놀 A 다이글리시딜 에테르 100중량부에 대하여, 1,4-부탄디올디글리시딜 에테르 20~40중량부를 포함하고,
상기 경화제는 탄산칼슘 100중량부에 대하여, 폴리(옥시프로필렌)디아민 15~40중량부, 비스페놀 A-비스페놀 A 디글리시딜 에테르 중합체 1~15중량부를 포함하는 무용제형 수용성 에폭시 바닥재.
The method of claim 1,
The subject contains 20 to 40 parts by weight of 1,4-butanediol diglycidyl ether based on 100 parts by weight of bisphenol A diglycidyl ether,
The curing agent, based on 100 parts by weight of calcium carbonate, poly (oxypropylene) diamine 15 to 40 parts by weight, bisphenol A-bisphenol A diglycidyl ether polymer 1 to 15 parts by weight of a solvent-free water-soluble epoxy flooring containing.
제1항에 있어서,
상기 주제 : 경화제는 1 : 1 ~ 1 : 3의 중량비로 포함되는 무용제형 수용성 에폭시 바닥재.
The method of claim 1,
The above subject: a solvent-free water-soluble epoxy flooring material containing a curing agent in a weight ratio of 1:1 to 1:3.
제1항에 있어서,
상기 탄산칼슘은 D1의 직경을 갖는 제1탄산칼슘, D2의 직경을 갖는 제2탄산칼슘, D3의 직경을 갖는 제3탄산칼슘을 포함하며,
D1〈 D2〈 D3 인 무용제형 수용성 에폭시 바닥재.
The method of claim 1,
The calcium carbonate includes first calcium carbonate having a diameter of D1, secondary calcium carbonate having a diameter of D2, and tertiary calcium carbonate having a diameter of D3,
Solvent-free water-soluble epoxy flooring with D1<D2< D3.
제1항에 있어서,
상기 탄산칼슘은 서로 다른 직경을 갖는 제1탄산칼슘, 제2탄산칼슘, 제3탄산칼슘을 포함하며,
제1탄산칼슘의 함량이 A, 제2탄산칼슘의 함량이 B, 제3탄산칼슘의 함량이 C라고 할 때, A 〈 B〈 C 인 무용제형 수용성 에폭시 바닥재.
The method of claim 1,
The calcium carbonate includes first calcium carbonate, second calcium carbonate, and third calcium carbonate having different diameters,
A solvent-free water-soluble epoxy flooring material with A < B < C when the content of primary calcium carbonate is A, the content of secondary calcium carbonate is B, and the content of tertiary calcium carbonate is C.
제1항에 있어서,
상기 경화제는 탄산칼슘 100중량부에 대하여, 2,4,6-트리스(다이메틸아미노메틸)페놀 0.1~15중량부를 더 포함하는 무용제형 수용성 에폭시 바닥재.
The method of claim 1,
The curing agent, based on 100 parts by weight of calcium carbonate, 2,4,6-tris (dimethylaminomethyl) phenol solvent-free water-soluble epoxy flooring further comprising 0.1 to 15 parts by weight.
KR1020200164476A 2020-11-30 2020-11-30 Solvent-free type water soluble epoxy flooring KR102476926B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1020200164476A KR102476926B1 (en) 2020-11-30 2020-11-30 Solvent-free type water soluble epoxy flooring

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1020200164476A KR102476926B1 (en) 2020-11-30 2020-11-30 Solvent-free type water soluble epoxy flooring

Publications (2)

Publication Number Publication Date
KR20220075886A true KR20220075886A (en) 2022-06-08
KR102476926B1 KR102476926B1 (en) 2022-12-14

Family

ID=81981555

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1020200164476A KR102476926B1 (en) 2020-11-30 2020-11-30 Solvent-free type water soluble epoxy flooring

Country Status (1)

Country Link
KR (1) KR102476926B1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102448907B1 (en) * 2022-06-29 2022-09-29 이재식 Lining composition and coating film construction method using the same
KR102511372B1 (en) 2022-12-28 2023-03-17 주식회사 명진화학 A method for producing a water-soluble epoxy composition containing nano-silica and a method for constructing a flooring material using the same

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102559263B1 (en) 2023-05-08 2023-07-25 동양에폭시 주식회사 Epoxy coating material for wood and coating method using the same

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100962259B1 (en) * 2009-11-19 2010-06-11 (주)그린텍컴 Water-soluble epoxy resin for thick coating
KR101076670B1 (en) * 2011-06-09 2011-10-26 (주)미성빌드 Water-soluble thick epoxy paint composition having antibacterial function and construction method using thereof
KR101263382B1 (en) * 2012-04-13 2013-05-21 (주)그린텍컴 Method of forming a coating layer using water-soluble epoxy resin mortar eco-friendly
KR101478946B1 (en) * 2014-03-28 2015-01-05 (주)동서에코라인 The waterproof construction method for concrete structure using the membrane agent
KR101540926B1 (en) * 2015-03-27 2015-08-06 (주)그린텍컴 Odor-free and Non-toxic Two Liquids Type of Epoxy Resin Based Composition and Method for Preparing the Same
KR20190074155A (en) * 2017-12-19 2019-06-27 주식회사 유니테크 Adhesive composition for automobility

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100962259B1 (en) * 2009-11-19 2010-06-11 (주)그린텍컴 Water-soluble epoxy resin for thick coating
KR101076670B1 (en) * 2011-06-09 2011-10-26 (주)미성빌드 Water-soluble thick epoxy paint composition having antibacterial function and construction method using thereof
KR101263382B1 (en) * 2012-04-13 2013-05-21 (주)그린텍컴 Method of forming a coating layer using water-soluble epoxy resin mortar eco-friendly
KR101478946B1 (en) * 2014-03-28 2015-01-05 (주)동서에코라인 The waterproof construction method for concrete structure using the membrane agent
KR101540926B1 (en) * 2015-03-27 2015-08-06 (주)그린텍컴 Odor-free and Non-toxic Two Liquids Type of Epoxy Resin Based Composition and Method for Preparing the Same
KR20190074155A (en) * 2017-12-19 2019-06-27 주식회사 유니테크 Adhesive composition for automobility

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102448907B1 (en) * 2022-06-29 2022-09-29 이재식 Lining composition and coating film construction method using the same
KR102511372B1 (en) 2022-12-28 2023-03-17 주식회사 명진화학 A method for producing a water-soluble epoxy composition containing nano-silica and a method for constructing a flooring material using the same

Also Published As

Publication number Publication date
KR102476926B1 (en) 2022-12-14

Similar Documents

Publication Publication Date Title
KR20220075886A (en) Solvent-free type water soluble epoxy flooring
SA516370362B1 (en) Intumescent coating composition
KR102042801B1 (en) Solvent-free epoxy coating composition
CN109890913A (en) Anti-flammability coating composition
KR101583731B1 (en) Paint composition for steel structure having steel bridge, and method for painting of steel structure using this same
KR101586980B1 (en) Repair-reinforcement method for concrete structure using polymer mortar comprising aramid fibers and surface protectant containing ceramic urethane
CN108034332A (en) A kind of Waterborne Fire Retardant Coatings for Steel and preparation method thereof
KR102341582B1 (en) Epoxy Coating Composition
SA516371615B1 (en) Water-based epoxy formulations for applied fireproofing
KR101937432B1 (en) Environmentally friendly water-soluble epoxy resin composition for preventing salt damage and neutralization of concrete structures and method of construction using the same
KR102067736B1 (en) Repair-reinforcement method for concrete structure using base coating material containing functional-aqueous epoxy, polymer mortar containing aramid fibers and surface protectant containing nano-size silver
KR102214479B1 (en) Water soluble elastic insulation waterproof agent and method for pavement marking using the same
KR101932242B1 (en) Aqueous epoxy coating agent and manufacturing method thereof and waterproof method using thereof
WO2016021915A1 (en) Composition for environment-friendly floor finishing material
KR101753523B1 (en) Epoxy paint composition having excellent noise reduction property for coating floor
KR101012000B1 (en) water-proof floor coating composition
KR102215875B1 (en) Epoxy Coating Composition
CN115612405A (en) Thick-coating type fireproof coating and preparation method thereof
JP2001342048A (en) Coating material for concrete and repairing or protecting method of concrete surface
KR101877635B1 (en) Water soluable paint composition
JP2009073879A (en) Water-based epoxy resin composition and coated floor
KR102133243B1 (en) Eco-friendly water-soluble coating material for medium corrosion and spray-type medium corrosion coating method using the same
CN112280342A (en) Inorganic anticorrosive fireproof coating and preparation method thereof
RU2489465C1 (en) Double-package composition for protective and decorative floor coating
US10118864B2 (en) Decorative coating compositions