KR100455761B1 - Water-based acrylic polymer having adhesion characteristic - Google Patents

Water-based acrylic polymer having adhesion characteristic Download PDF

Info

Publication number
KR100455761B1
KR100455761B1 KR10-2001-0063458A KR20010063458A KR100455761B1 KR 100455761 B1 KR100455761 B1 KR 100455761B1 KR 20010063458 A KR20010063458 A KR 20010063458A KR 100455761 B1 KR100455761 B1 KR 100455761B1
Authority
KR
South Korea
Prior art keywords
monomer
weight
parts
adhesive
acid
Prior art date
Application number
KR10-2001-0063458A
Other languages
Korean (ko)
Other versions
KR20030031364A (en
Inventor
오상택
김구니
이규찬
Original Assignee
한국신발피혁연구소
이규찬
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 한국신발피혁연구소, 이규찬 filed Critical 한국신발피혁연구소
Priority to KR10-2001-0063458A priority Critical patent/KR100455761B1/en
Publication of KR20030031364A publication Critical patent/KR20030031364A/en
Application granted granted Critical
Publication of KR100455761B1 publication Critical patent/KR100455761B1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C09J133/04—Homopolymers or copolymers of esters
    • C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09J133/08—Homopolymers or copolymers of acrylic acid esters
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C09J133/04—Homopolymers or copolymers of esters
    • C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09J133/10—Homopolymers or copolymers of methacrylic acid esters
    • C09J133/12—Homopolymers or copolymers of methyl methacrylate
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C09J133/18—Homopolymers or copolymers of nitriles
    • C09J133/20—Homopolymers or copolymers of acrylonitrile
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J9/00—Adhesives characterised by their physical nature or the effects produced, e.g. glue sticks

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

본 발명은 아크릴계 에멀젼형 접착성 고분자에 관한 것으로서, 더욱 상세하게는 응집성 단량체 및 점착성 단량체의 조성을 변화시켜 유리전이 온도와 극성을 변화시키고 가교 가능한 작용기를 갖는 단량체로 에틸렌계 불포화 카르본산 단량체를 사용하여 합성된 아크릴계 에멀젼형 접착성 고분자 및 이 고분자로 제조된 상태 접착력 및 내수 접착력이 우수한 접착제에 관한 것이다.The present invention relates to an acrylic emulsion-type adhesive polymer, and more particularly, using an ethylenically unsaturated carboxylic acid monomer as a monomer having a crosslinkable functional group and a glass transition temperature and polarity by changing the composition of the cohesive monomer and the adhesive monomer. The present invention relates to a synthetic acrylic emulsion-type adhesive polymer and an adhesive excellent in state adhesiveness and water resistance adhesiveness prepared from the polymer.

Description

아크릴계 에멀젼형 접착성 고분자{Water-based acrylic polymer having adhesion characteristic}Water-based acrylic polymer having adhesion characteristic

본 발명은 아크릴계 에멀젼형 접착성 고분자에 관한 것으로서, 더욱 상세하게는 응집성 단량체 및 점착성 단량체의 조성을 변화시켜 유리전이 온도와 극성을 변화시키고 가교 가능한 작용기를 갖는 단량체로 에틸렌계 불포화 카르본산 단량체를 사용하여 합성된 아크릴계 에멀젼형 접착성 고분자 및 이 고분자로 제조된 상태 접착력 및 내수 접착력이 우수한 접착제에 관한 것이다.The present invention relates to an acrylic emulsion-type adhesive polymer, and more particularly, using an ethylenically unsaturated carboxylic acid monomer as a monomer having a crosslinkable functional group and a glass transition temperature and polarity by changing the composition of the cohesive monomer and the adhesive monomer. The present invention relates to a synthetic acrylic emulsion-type adhesive polymer and an adhesive excellent in state adhesiveness and water resistance adhesiveness prepared from the polymer.

타일용 접착제는 수성형과 반응형으로 대별된다. 수성형은 아크릴 에멀젼이나 스티렌-부타디엔 라텍스(SB latex)를 기본 수지로 하고 충진제, 점착부여수지, 유기용제, 가소제 등을 혼합하여 제조되는 페이스트상의 일액형 접착제가 사용된다. 반응형은 우레탄 수지 또는 에폭시 수지를 기본으로 하여 각종 첨가제를 혼합하여 이액형으로 사용된다.Adhesives for tiles are roughly classified into aqueous and reactive forms. As the aqueous type, a paste-type one-component adhesive prepared by mixing an acrylic emulsion or styrene-butadiene latex (SB latex) as a base resin and a filler, a tackifying resin, an organic solvent, and a plasticizer is used. Reaction type is used as two-component type by mixing various additives based on urethane resin or epoxy resin.

수성형 접착제는 공해 및 화재의 위험성이 낮고 사용하기가 간편하여 현장에서 시공하는 타일용 접착제의 주류를 이루고 있다. 그러나, 내수성이 좋지 못하여물을 많이 사용하는 곳에서는 사용이 어려운 한계점이 있다.Water-based adhesives have a low risk of pollution and fire and are easy to use, making the mainstream of tile adhesives for construction in the field. However, where the water resistance is not good, the use of a lot of water has a difficult point of use.

이에, 본 발명자들은 타일용 수성 접착제의 내수성을 향상시키기 위하여 접착성 고분자인 아크릴계 에멀젼을 합성하였고 이를 이용하여 접착제를 제조함으로써 본 발명을 완성하게 되었다.Thus, the present inventors synthesized an acrylic emulsion, which is an adhesive polymer, in order to improve the water resistance of the water-based adhesive for tiles, and completed the present invention by preparing the adhesive using the same.

따라서, 본 발명은 우수한 상태 접착력 및 내수 접착력을 가지는 아크릴계 에멀젼 접착제를 제공하는데 그 목적이 있다.Accordingly, an object of the present invention is to provide an acrylic emulsion adhesive having excellent state adhesion and water resistance.

본 발명은 이중결합을 갖는 단량체를 유화중합하여 제조한 아크릴계 에멀젼 접착성 고분자에 있어서,상기 이중결합을 갖는 단량체 100 중량부 중에는, 응집성 단량체 20 ∼ 60 중량부, 점착성 단량체 20 ∼ 80 중량부, 에틸렌계 불포화 카르본산 단량체 0.1 ∼ 20 중량부가 포함되어 있고,상기한 단량체를 유화중합하여 제조한 것으로 유리전이온도가 -25 ∼ 15 ℃ 범위인 아크릴계 에멀젼 접착성 고분자를 그 특징으로 한다.The present invention is an acrylic emulsion adhesive polymer prepared by emulsion polymerization of a monomer having a double bond, in 100 parts by weight of the monomer having a double bond, 20 to 60 parts by weight of cohesive monomer, 20 to 80 parts by weight of adhesive monomer, ethylene 0.1 to 20 parts by weight of the unsaturated unsaturated carboxylic acid monomer is contained, and is prepared by the emulsion polymerization of the above-mentioned monomer, characterized in that the acrylic emulsion adhesive polymer having a glass transition temperature of -25 ~ 15 ℃ range.

또한, 상기 아크릴계 에멀젼형 접착성 고분자로 제조된 접착제를 포함한다.It also includes an adhesive made of the acrylic emulsion adhesive polymer.

이와 같은 본 발명을 상세히 설명하면 다음과 같다.The present invention will be described in detail as follows.

본 발명에 따른 아크릴계 에멀젼 접착성 고분자는 응집성 단량체, 점착성 단량체, 카르복실기를 갖는 가교성 단량체, 개시제 및 유화제를 사용하여 유화중합시켜 제조한다.The acrylic emulsion adhesive polymer according to the present invention is prepared by emulsion polymerization using a cohesive monomer, an adhesive monomer, a crosslinkable monomer having a carboxyl group, an initiator and an emulsifier.

본 발명에 사용될 수 있는 응집성 단량체로서는 메틸아크릴레이트, 메틸메타크릴레이트, 에틸아크릴레이트, 에틸메타크릴레이트, 부틸메타크릴레이트, 시클로헥실 메타크릴레이트, 아크릴로니트릴, 메타크릴로니트릴, 비닐아세테이트 중에서 선택된 1종 또는 2종 이상이 바람직하며, 전체 단량체 사용량 100 중량부에 대하여 응집성 단량체는 20 ∼ 60 중량부를 함유한다. 이때 20 중량부 미만이면 얻어지는 중합체의 응집력이 낮아서 접착력이 저하하는 문제점이 있고, 60 중량부를 초과하면 에멀젼 중합체의 합성이 용이하지 않으며 유리전이온도가 높아져서 에멀젼 자체의 피막 형성이 어렵게 되고 따라서 접착력이 저하하는 문제가 있다.Cohesive monomers that can be used in the present invention include methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, butyl methacrylate, cyclohexyl methacrylate, acrylonitrile, methacrylonitrile, and vinyl acetate. One or two or more selected are preferable, and the cohesive monomer contains 20 to 60 parts by weight based on 100 parts by weight of the total amount of monomers used. At this time, if the content is less than 20 parts by weight, there is a problem in that the adhesive strength is lowered due to the low cohesive strength of the obtained polymer. If the content is more than 60 parts by weight, the synthesis of the emulsion polymer is not easy, and the glass transition temperature is increased, making the film of the emulsion itself difficult. There is a problem.

또한, 점착성 단량체로는 부틸아크릴레이트, 2-에틸헥실아크릴레이트, 헥실아크릴레이트, 프로필아크릴레이트 중에서 선택된 1종 또는 2종 이상이 바람직하다. 상기 전체 단량체 사용량 100 중량부에 대하여 점착성 단량체는 20 ∼ 80 중량부를 함유한다. 이때 20 중량부 미만이면 점착성이 낮아서 초기 부착력이 저하되는 문제점이 있고, 80 중량부를 초과하면 접착제의 기능보다는 점착제의 특성이 우세하게 나타나서 초기 부착성은 증가하지만 응집력 저하로 인한 접착력이 저하하는 문제가 있다.Moreover, 1 type (s) or 2 or more types chosen from a butyl acrylate, 2-ethylhexyl acrylate, hexyl acrylate, and propyl acrylate are preferable as an adhesive monomer. The adhesive monomer contains 20 to 80 parts by weight based on 100 parts by weight of the total amount of the monomer used. At this time, if less than 20 parts by weight, the adhesiveness is low, there is a problem that the initial adhesive strength is lowered, if it exceeds 80 parts by weight, the properties of the adhesive is superior to the function of the adhesive appears to increase the initial adhesiveness, but there is a problem that the adhesive strength due to the decrease in cohesion .

본 발명에서는 분자쇄 중에 카르복실기의 도입을 위하여 전체 단량체 사용량100 중량부에 대하여 0.1 ∼ 20 중량부 범위 내에서, 바람직하기는 0.5 ∼ 10 중량부의 에틸렌계 불포화 카르본산 단량체를 사용할 수 있으며, 불포화 카르본산 단량체로서는 아크릴산, 메타크릴산, 크로톤산, 말레인산, 푸말산 및 이타콘산 중에서 선택된 1종 또는 2종 이상을 들 수 있다. 0.1 중량부 미만 사용하게 되면 내수성의 향상에 기여하지 못하며 20 중량부를 초과하면 에멀젼 합성시 겔화가 진행되므로 바람직하지 못하다.In the present invention, within the range of 0.1 to 20 parts by weight, preferably 0.5 to 10 parts by weight of an ethylenically unsaturated carboxylic acid monomer, based on 100 parts by weight of the total amount of monomers used for introduction of carboxyl groups in the molecular chain, and unsaturated carboxylic acids. As a monomer, 1 type, or 2 or more types chosen from acrylic acid, methacrylic acid, crotonic acid, maleic acid, fumaric acid, and itaconic acid are mentioned. If it is used less than 0.1 parts by weight does not contribute to the improvement of water resistance, if it exceeds 20 parts by weight it is not preferable because the gelation proceeds in the synthesis of the emulsion.

중합반응은 통상의 유화중합방법에 의하며, 유화중합용 개시제로서는 일반적인 유화중합용 개시제는 모두 사용될 수 있다. 특히, 바람직하기로는 과황산암모늄, 과황산칼륨, 과황산나트륨, t-부틸히드로퍼옥시드 등을 0.1 ∼ 5 중량부를 사용한다. 이때, 0.1 중량부 미만을 사용하면 개시제의 효율이 저하하여 반응이 쉽게 진행되지 못하므로 에멀젼 중합체의 합성이 어려운 문제가 있고, 5 중량부를 초과 사용하면 순간적인 발열반응에 의하여 겔이 생성되는 문제점이 있다.The polymerization reaction is carried out by a conventional emulsion polymerization method, and any initiator for emulsion polymerization may be used as the initiator for emulsion polymerization. In particular, 0.1 to 5 parts by weight of ammonium persulfate, potassium persulfate, sodium persulfate, t-butylhydroperoxide and the like are preferably used. At this time, if less than 0.1 parts by weight, the efficiency of the initiator is lowered because the reaction is not easily progressed, there is a problem that the synthesis of the emulsion polymer is difficult, and if more than 5 parts by weight of the gel is generated by the instantaneous exothermic reaction have.

유화제 역시 한정되지는 않으며 음이온성 및 비이온성 유화제를 병용하는 것이 좋다. 이들 유화제는 전체 단량체 사용량 100 중량부에 대하여 0.1 ∼ 20 중량부, 바람직하기는 1 ∼ 10 중량부가 좋다. 0.1 중량부 미만 사용하게 되면 에멀젼의 합성이 용이하지 않으며 20 중량부를 초과하면 내수성이 저하되는 단점이 있다.The emulsifier is also not limited, and it is preferable to use anionic and nonionic emulsifiers in combination. These emulsifiers are preferably 0.1 to 20 parts by weight, preferably 1 to 10 parts by weight based on 100 parts by weight of the total amount of monomers. If it is used less than 0.1 parts by weight of the synthesis of the emulsion is not easy, if more than 20 parts by weight has a disadvantage in that the water resistance is lowered.

본 발명에서 사용될 수 있는 비이온계 계면활성제의 예로서는 폴리옥시에틸렌라우릴에테르, 폴리옥시에틸렌스테아릴에테르, 폴리옥시에틸렌세틸에테르 등의 폴리옥시에틸렌알킬에테르, 폴리옥시에틸렌옥틸페닐에테르 등의 폴리옥시에틸렌알킬아릴에테르, 폴리옥시에틸렌 유도체, 옥시에틸렌·옥시프로필렌 블록 공중합체, 글리세린지방산에스테르, 폴리옥시에틸렌지방산에스테르 등을 사용할 수 있다. 음이온성 계면활성제로는 폴리옥시에틸렌 노닐페닐 에테르 황산암모늄, 도데실벤젠술폰산소다, 라우릴황산나트륨 등을 들 수 있다. 특히, 계면활성제로는 폴리옥시에틸렌알킬아릴에테르, 폴리옥시에틸렌 노닐페닐 에테르 황산암모늄, 도데실벤젠술폰산소다 등이 바람직하다.Examples of nonionic surfactants that can be used in the present invention include polyoxyethylene lauryl ether, polyoxyethylene stearyl ether, polyoxyethylene alkyl ether such as polyoxyethylene cetyl ether, and polyoxy such as polyoxyethylene octylphenyl ether. Ethylene alkyl aryl ether, a polyoxyethylene derivative, an oxyethylene oxypropylene block copolymer, glycerin fatty acid ester, polyoxyethylene fatty acid ester, etc. can be used. Examples of the anionic surfactants include polyoxyethylene nonylphenyl ether ammonium sulfate, sodium dodecylbenzene sulfonate, sodium lauryl sulfate and the like. In particular, as the surfactant, polyoxyethylene alkyl aryl ether, polyoxyethylene nonylphenyl ether ammonium sulfate, dodecyl benzene sulfonate and the like are preferable.

상기와 같은 조성으로 합성된 아크릴계 에멀젼형 접착성 고분자를 이용하여 타일용 수성 접착제를 제조한다. 또한, 아크릴 에멀젼의 전화율, 유리전이온도, 상태 접착강도 및 내수 접착강도를 측정한 결과, 아크릴 에멀젼의 전화율은 99.5% 이상, 유리전이온도는 -25 ∼ 15 ℃이며, 접착제의 상태 접착력 및 내수 접착력은 매우 우수하게 나타났다.Using the acrylic emulsion-type adhesive polymer synthesized in the composition as described above to prepare an aqueous adhesive for tiles. In addition, the conversion rate, glass transition temperature, state adhesive strength and water resistance of the acrylic emulsion were measured. As a result, the conversion rate of the acrylic emulsion was 99.5% or more and the glass transition temperature was -25 to 15 ° C. Appeared very excellent.

이하, 본 발명을 다음 실시예에 의거하여 더욱 상세히 설명하겠는 바, 본 발명에 이에 한정되는 것은 아니다.Hereinafter, the present invention will be described in more detail based on the following examples, which are not intended to limit the present invention.

제조예: 에멀젼 합성Preparation Example: Emulsion Synthesis

다음 표 1의 조성에 따라 단량체와 유화제를 칭량한 후 1000 rpm으로 교반하여 단량체 유화액을 얻었다. 교반기, 냉각기, 온도계, 적하깔대기, 질소 주입 장치가 장착된 6구 분리형 반응기에 물 107 g을 가하고 질소분위기 하에서 교반하면서 80 ℃로 유지시켰다. 개시제와 단량체 유화물을 5 시간에 걸쳐 적하하였다. 적하가 끝난 후 1시간 30분 동안 더 교반하고 40 ℃ 이하로 냉각하여 반응을 종료하였다.Next, the monomer and the emulsifier were weighed according to the composition of Table 1 and stirred at 1000 rpm to obtain a monomer emulsion. 107 g of water was added to a six-necked separate reactor equipped with a stirrer, a cooler, a thermometer, a dropping funnel, and a nitrogen injector, and maintained at 80 ° C. under stirring in a nitrogen atmosphere. The initiator and monomer emulsion were added dropwise over 5 hours. After the addition was completed, the mixture was further stirred for 1 hour and 30 minutes, cooled to 40 ° C or less, and the reaction was completed.

구 분division 합성예 1Synthesis Example 1 합성예 2Synthesis Example 2 합성예 3Synthesis Example 3 합성예 4Synthesis Example 4 합성예 5Synthesis Example 5 합성예 6Synthesis Example 6 아크릴로니트릴(g)Acrylonitrile (g) 77 88 3030 22 22 55 메틸메타릴레이트(g)Methyl methacrylate (g) 3535 19.519.5 1010 55 55 77 비닐아세테이트(g)Vinyl acetate (g) 33 -- 55 88 88 44 에틸메타크릴레이트(g)Ethyl methacrylate (g) -- 22 -- 44 44 33 부틸아크릴레이트(g)Butyl acrylate (g) 2727 34.534.5 2727 4545 4545 3535 2-에틸헥실아크릴레이트(g)2-ethylhexyl acrylate (g) 2727 3535 2727 3535 3535 4545 아크릴산(g)Acrylic acid (g) -- -- 1One -- 1One 1One 메타크릴산(g)Methacrylic acid (g) 1One 1One -- -- -- -- 음이온성 계면활성제(g)Anionic Surfactant (g) 2.12.1 2.12.1 2.12.1 2.12.1 2.12.1 2.12.1 비이온성 계면활성제(g)Nonionic surfactant (g) 4.94.9 4.94.9 4.94.9 4.94.9 4.94.9 4.94.9

실시예 1 ∼ 3 및 비교예 1 ∼ 4Examples 1-3 and Comparative Examples 1-4

1. 접착제 제조1. glue manufacturer

다음 표 2의 조성에 따라 타일용 수성 접착제를 제조하였다.Next, an aqueous adhesive for tiles was prepared according to the composition of Table 2.

셀룰로오스[준세이, 일본] 2 g을 물 100 g에 용해시키고 합성된 아크릴 에멀젼, 계면활성제로 NP-1020[동남합성㈜] 1 g 및 가소제로 DBP(디부틸프탈레리트)[준세이, 일본] 3 g을 첨가하여 균일하게 교반하였다. 탄산칼슘[준세이, 일본] 200 g을 첨가하여 진흙반죽 상태가 되도록 교반하였다. 마지막으로 수산화암모늄[준세이, 일본] 3 g을 첨가하고 1시간동안 교반하여 접착제를 제조하였다.2 g of cellulose [Junsei, Japan] was dissolved in 100 g of water, a synthetic acrylic emulsion, 1 g of NP-1020 [Dongnam Synthetic Co., Ltd.] as a surfactant, and DBP (dibutyl phthalate) as a plasticizer [Junsei, Japan] 3 g was added and stirred uniformly. 200 g of calcium carbonate [Junsei, Japan] was added, and it stirred so that it might become mud dough. Finally, 3 g of ammonium hydroxide [Junsei, Japan] was added and stirred for 1 hour to prepare an adhesive.

조 성Furtherance 실시예 1Example 1 실시예 2Example 2 실시예 3Example 3 비교예 1Comparative Example 1 비교예 2Comparative Example 2 비교예 3Comparative Example 3 비교예 4Comparative Example 4 아크릴 에멀젼(g)Acrylic Emulsion (g) 합성예 1Synthesis Example 1 100100 -- -- -- -- -- -- 합성예 2Synthesis Example 2 -- 100100 -- -- -- -- -- 합성예 3Synthesis Example 3 -- -- 100100 -- -- -- -- 합성예 4Synthesis Example 4 -- -- -- 100100 -- -- -- 합성예 5Synthesis Example 5 -- -- -- -- 100100 -- -- 합성예 6Synthesis Example 6 -- -- -- -- -- 100100 -- 스티렌-부타디엔 라텍스* Styrene-butadiene latex * -- -- -- -- -- -- 100100 * KOSYL KSL 341 (금호석유화학㈜)* KOSYL KSL 341 (Kumho Petrochemical Co., Ltd.)

2. 시편 몰타르 제조2. Specimen Maltar Manufacturing

다음 표 3의 조성(KSL 1593)에 따라 배합한 후 상온에서 24시간 양생하고 이를 상온의 물속에서 다시 6일간 양생하였다. 몰타르를 물에서 건져내고 상온에서 7일간 양생한 후 150번 연마지로 표면을 연마하여 시편 몰타르를 제조하였다.After blending according to the composition of Table 3 (KSL 1593) and curing for 24 hours at room temperature, it was again cured in water at room temperature for 6 days. After the mortar was removed from the water and cured at room temperature for 7 days, a specimen mortar was prepared by grinding the surface with the abrasive paper No. 150.

몰타르의 조성Composition of maltar 종류Kinds 무게weight 시멘트(g)Cement (g) 520520 모래(g)Sand (g) 10401040 물(g)Water (g) 338338 ABAB 접착제와 타일의 경계면Interface between glue and tile

시험예 1: 아크릴 에멀젼의 전화율 측정Test Example 1: Conversion of Acrylic Emulsion

합성한 아크릴 에멀젼을 120 ℃의 적외선 건조기에서 2시간 동안 건조한 후 잔량을 고형분으로 보고, 다음 수학식 1을 이용하여 전화율을 계산하였다.The synthesized acrylic emulsion was dried in an infrared dryer at 120 ° C. for 2 hours, and the residual amount was reported as solids. Then, the conversion ratio was calculated using Equation 1 below.

시험예 2 : 접착강도측정Test Example 2: Adhesion Strength Measurement

1. 상태 접착강도1. State adhesive strength

상태 접착강도는 몰타르에 접착제를 빗으로 도포한 후 타일을 접착하고 실온에서 8시간 방치하였다. 다시 40 ℃에서 2일간 양생하여 만능인장 시험기[독일, 쯔빅사]로 측정하였다. 이때 인장 속도는 3 mm/min로 하였다.The adhesive strength of the state was applied to the mortar with a comb, and then the tiles were bonded and left at room temperature for 8 hours. It was cured again at 40 ° C. for 2 days and measured with a universal tensile tester [Zwick, Germany]. At this time, the tensile velocity was 3 mm / min.

2. 내수 접착강도2. Waterproofing strength of water

몰타르에 접착제를 빗으로 도포한 후 타일을 접착하고 40 ℃에서 2일간 양생된 시편을 실온의 수산화칼슘 포화용액에 2일간 침지한 후 꺼내어 즉시 만능인장 시험기로 측정하였다. 이때 인장 속도는 3 mm/min로 하였다.The adhesive was applied to the mortar with a comb, and the tiles were adhered. The specimens cured for 2 days at 40 ° C. were immersed in a saturated calcium hydroxide solution at room temperature for 2 days, and then taken out and immediately measured by a universal tensile tester. At this time, the tensile velocity was 3 mm / min.

구 분division 실시예 1Example 1 실시예 2Example 2 실시예 3Example 3 비교예 1Comparative Example 1 비교예 2Comparative Example 2 비교예 3Comparative Example 3 비교예 4Comparative Example 4 전화율(%)% Conversion 100100 100100 99.599.5 99.899.8 100100 100100 -- 에멀젼의 Tg(℃)Tg of the emulsion (° C.) -5.2-5.2 -24.9-24.9 -7.5-7.5 -40.9-40.9 -40.0-40.0 -39.2-39.2 -- 상태 접착강도(kgf/cm2)State Adhesive Strength (kgf / cm 2 ) 8.18.1 7.97.9 8.48.4 5.15.1 5.55.5 4.14.1 4.64.6 내수 접착강도(kgf/cm2)Water Resistance Adhesive Strength (kgf / cm 2 ) 2.62.6 1.91.9 2.22.2 0.10.1 0.60.6 0.30.3 0.20.2

상기 표 4에 나타낸 바와 같이, 실시예가 비교예에 비해 상태 접착력 및 내수 접착력이 매우 우수함을 알 수 있었다.As shown in Table 4, it can be seen that the Example is very excellent in the state adhesive strength and the water resistant adhesive strength compared to the comparative example.

이상에서 설명한 바와 같이, 본 발명의 아크릴계 에멀젼 접착성 고분자는 응집성 단량체와 점착성 단량체의 조성을 변화시켜 유리전이 온도와 극성을 변화시키고 가교 가능한 작용기를 갖는 단량체를 적절히 사용함으로써 매우 우수한 상태 접착력 및 내수 접착력을 발현할 수 있는 기능을 부여한다.As described above, the acrylic emulsion adhesive polymer of the present invention can change the composition of the cohesive monomer and the adhesive monomer to change the glass transition temperature and polarity, and use a monomer having a crosslinkable functional group so that excellent adhesiveness and water resistance can be obtained. Gives the ability to express.

Claims (4)

이중결합을 갖는 단량체를 유화중합하여 제조한 아크릴계 에멀젼 접착성 고분자에 있어서,In the acrylic emulsion adhesive polymer prepared by emulsion polymerization of a monomer having a double bond, 상기 이중결합을 갖는 단량체 100 중량부 중에는, 메틸메타크릴레이트, 아크릴로니트릴, 에틸메타크릴레이트 및 비닐아세테이트 중에서 선택된 1종 또는 2종 이상의 응집성 단량체 20 ∼ 60 중량부,In 100 parts by weight of the monomer having a double bond, 20 to 60 parts by weight of one or two or more cohesive monomers selected from methyl methacrylate, acrylonitrile, ethyl methacrylate, and vinyl acetate, 2-에틸헥실아크릴레이트 및 부틸아크릴레이트 중에서 선택된 1종 또는 2종 의 점착성 단량체 20 ∼ 80 중량부,20 to 80 parts by weight of one or two sticky monomers selected from 2-ethylhexyl acrylate and butyl acrylate, 아크릴산, 메타크릴산, 크로톤산, 말레인산, 푸말산 및 이타콘산 중에서 선택된 1종 또는 2종 이상의 에틸렌계 불포화 카르본산 단량체 0.1 ∼ 20 중량부가 포함되어 있고,0.1-20 parts by weight of one or two or more ethylenically unsaturated carboxylic acid monomers selected from acrylic acid, methacrylic acid, crotonic acid, maleic acid, fumaric acid and itaconic acid, 상기한 단량체를 유화중합하여 제조한 것으로 유리전이온도가 -25 ∼ 15 ℃ 범위인 것임을 특징으로 하는 아크릴계 에멀젼 접착성 고분자.Acrylic emulsion adhesive polymer prepared by emulsion polymerization of the above monomers, characterized in that the glass transition temperature is in the range of -25 ~ 15 ℃. 삭제delete 삭제delete 청구항 1의 아크릴계 에멀젼 접착성 고분자를 이용하여 제조된 타일용 수성 접착제.Aqueous adhesive for tiles manufactured using the acrylic emulsion adhesive polymer of claim 1.
KR10-2001-0063458A 2001-10-15 2001-10-15 Water-based acrylic polymer having adhesion characteristic KR100455761B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR10-2001-0063458A KR100455761B1 (en) 2001-10-15 2001-10-15 Water-based acrylic polymer having adhesion characteristic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR10-2001-0063458A KR100455761B1 (en) 2001-10-15 2001-10-15 Water-based acrylic polymer having adhesion characteristic

Publications (2)

Publication Number Publication Date
KR20030031364A KR20030031364A (en) 2003-04-21
KR100455761B1 true KR100455761B1 (en) 2004-11-15

Family

ID=29564692

Family Applications (1)

Application Number Title Priority Date Filing Date
KR10-2001-0063458A KR100455761B1 (en) 2001-10-15 2001-10-15 Water-based acrylic polymer having adhesion characteristic

Country Status (1)

Country Link
KR (1) KR100455761B1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101366102B1 (en) * 2012-05-24 2014-02-28 한국신발피혁연구원 Primer composition for difficulty adhesion material

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20030043070A (en) * 2001-11-26 2003-06-02 건설화학공업(주) 1-Component Room Temperature-Cross linkable Emulsion Composition
KR20060046287A (en) 2004-05-31 2006-05-17 가부시키가이샤 닛폰 쇼쿠바이 Emulsion, production method thereof and use thereof
CN100400612C (en) * 2005-09-19 2008-07-09 北京高盟化工有限公司 Prepn of water-base composite acrylic adhesive
KR100868078B1 (en) * 2008-03-12 2008-11-11 주식회사 휴다임건축사사무소 Adhesion composition of emulsion-type for mixing with cement mortar having eco-friendly
WO2014093273A1 (en) * 2012-12-10 2014-06-19 Avery Dennison Corporation Rf activatable adhesives and applications thereof
CN115216256B (en) * 2022-08-15 2024-02-20 衡水新光新材料科技有限公司 High-performance ceramic tile adhesive

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06220414A (en) * 1993-01-22 1994-08-09 Kuraray Co Ltd Adhesive composition for tile
KR970042906A (en) * 1995-12-29 1997-07-26 김충세 Adhesive composition
KR0165527B1 (en) * 1996-07-09 1999-01-15 박상욱 Acryl-emulsion adhesvie composition
KR20000030217A (en) * 2000-02-10 2000-06-05 진기창 Adhesive of two component acrylic urethane emulsion
KR20030015565A (en) * 2001-08-16 2003-02-25 주식회사 리콘스 Water soluble tile adhesive agent

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06220414A (en) * 1993-01-22 1994-08-09 Kuraray Co Ltd Adhesive composition for tile
KR970042906A (en) * 1995-12-29 1997-07-26 김충세 Adhesive composition
KR0165527B1 (en) * 1996-07-09 1999-01-15 박상욱 Acryl-emulsion adhesvie composition
KR20000030217A (en) * 2000-02-10 2000-06-05 진기창 Adhesive of two component acrylic urethane emulsion
KR20030015565A (en) * 2001-08-16 2003-02-25 주식회사 리콘스 Water soluble tile adhesive agent

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101366102B1 (en) * 2012-05-24 2014-02-28 한국신발피혁연구원 Primer composition for difficulty adhesion material

Also Published As

Publication number Publication date
KR20030031364A (en) 2003-04-21

Similar Documents

Publication Publication Date Title
US9950954B2 (en) Two component cement composition
EP1048676B1 (en) Polymer compositions
CN103476730B (en) The painted latex composition of high solid
CN106715491A (en) A dispersion of (meth)acrylate copolymer containing a hydroxyalkyl (meth)acrylate functional monomer unit for flexible cementitious waterproofing materials
JP2008540718A (en) Use of silicon-containing polymers as building adhesives
JPH0742376B2 (en) Curable composition
NO831898L (en) DIFFERENT ARTIFICIAL DISTRIBUTION BASED ON A COPOLYMER OF OLEFINICALLY SATURDED COMPOUNDS
JPWO2016163434A1 (en) Primer composition and method for producing the same
CN109181595A (en) A kind of ceramic tile gum and preparation method thereof and application method
CN101679707A (en) Copolymer mixture
KR100455761B1 (en) Water-based acrylic polymer having adhesion characteristic
CN104870498A (en) Plasticizer free caulks and sealants comprising waterborne acrylic polymeric composites and methods for making the same
JPH10231325A (en) Acrylic polymer and resin composition containing the same polymer
CN108026193A (en) For elasticity building gap filler and the multistage copolymer compositions of sealant
CN109836876A (en) A kind of road aqueous double-deck modified luminous paint of silicon fiml grafting and its preparation method and application
CN100467416C (en) Redispersible polymer viscose glue powder and preparation method thereof
CN104364218A (en) Re-emulsifiable synthetic resin powder composition for polymer cement and polymer cement mortar formed using same
JPH11189764A (en) Adhesive composition for tile
EP3034481B1 (en) Aqueous resin dispersion for mortar, mortar composition and hardened mortar product
CA2618043A1 (en) Adhesive for nonceramic floor coverings
JP2646305B2 (en) Base emulsion for adhesives
JPH01126251A (en) Cement composition
JPH07102232A (en) Hardenable pressure-sensitive adhesive of water-base emulsion type
JP2003171157A (en) Polymer emulsion for cement mortar and cement mortar composition
WO2023107204A1 (en) Acrylic copolymer compositions for use as sealants

Legal Events

Date Code Title Description
A201 Request for examination
E902 Notification of reason for refusal
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 20121025

Year of fee payment: 9

FPAY Annual fee payment

Payment date: 20131025

Year of fee payment: 10

LAPS Lapse due to unpaid annual fee