KR100657020B1 - Water Soluble Asphalt Waterproofing Agent For Waterproofing Film Formation - Google Patents
Water Soluble Asphalt Waterproofing Agent For Waterproofing Film Formation Download PDFInfo
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- KR100657020B1 KR100657020B1 KR1020050130161A KR20050130161A KR100657020B1 KR 100657020 B1 KR100657020 B1 KR 100657020B1 KR 1020050130161 A KR1020050130161 A KR 1020050130161A KR 20050130161 A KR20050130161 A KR 20050130161A KR 100657020 B1 KR100657020 B1 KR 100657020B1
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- asphalt
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- waterproofing agent
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- waterproofing
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- 238000004078 waterproofing Methods 0.000 title claims abstract description 65
- 239000010426 asphalt Substances 0.000 title claims abstract description 62
- 239000003795 chemical substances by application Substances 0.000 title claims abstract description 49
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title abstract description 20
- 230000015572 biosynthetic process Effects 0.000 title description 2
- 239000011248 coating agent Substances 0.000 claims abstract description 31
- 238000000576 coating method Methods 0.000 claims abstract description 31
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 22
- 239000000178 monomer Substances 0.000 claims abstract description 22
- 239000000839 emulsion Substances 0.000 claims abstract description 21
- 239000011347 resin Substances 0.000 claims abstract description 20
- 229920005989 resin Polymers 0.000 claims abstract description 20
- 239000000203 mixture Substances 0.000 claims abstract description 13
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 8
- 125000004427 diamine group Chemical group 0.000 claims abstract description 8
- 239000000126 substance Substances 0.000 claims abstract description 8
- 229920000178 Acrylic resin Polymers 0.000 claims abstract description 7
- 239000004925 Acrylic resin Substances 0.000 claims abstract description 7
- 239000002253 acid Substances 0.000 claims abstract description 6
- 238000004132 cross linking Methods 0.000 claims abstract description 6
- 125000000129 anionic group Chemical group 0.000 claims description 4
- 125000002091 cationic group Chemical group 0.000 claims description 4
- 230000000379 polymerizing effect Effects 0.000 claims 1
- 238000001035 drying Methods 0.000 abstract description 13
- 230000036314 physical performance Effects 0.000 abstract description 5
- 238000004904 shortening Methods 0.000 abstract description 3
- 239000011387 rubberized asphalt concrete Substances 0.000 description 11
- 238000010276 construction Methods 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 239000003505 polymerization initiator Substances 0.000 description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- 229920005731 JONCRYL® 67 Polymers 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 230000003472 neutralizing effect Effects 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- HXHCOXPZCUFAJI-UHFFFAOYSA-N prop-2-enoic acid;styrene Chemical compound OC(=O)C=C.C=CC1=CC=CC=C1 HXHCOXPZCUFAJI-UHFFFAOYSA-N 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- IBVAQQYNSHJXBV-UHFFFAOYSA-N adipic acid dihydrazide Chemical compound NNC(=O)CCCCC(=O)NN IBVAQQYNSHJXBV-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000003111 delayed effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002085 enols Chemical group 0.000 description 2
- -1 ethyl acrylate ester Chemical class 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 description 2
- 230000003014 reinforcing effect Effects 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- IBDVWXAVKPRHCU-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCOC(=O)C(C)=C IBDVWXAVKPRHCU-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002081 enamines Chemical class 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 229920002681 hypalon Polymers 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229920006173 natural rubber latex Polymers 0.000 description 1
- 238000010428 oil painting Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- XUCQTRUISKSFOC-UHFFFAOYSA-N prop-2-enoyl 3-oxobutaneperoxoate Chemical compound CC(=O)CC(=O)OOC(=O)C=C XUCQTRUISKSFOC-UHFFFAOYSA-N 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- 230000003252 repetitive effect Effects 0.000 description 1
- 239000010454 slate Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920006174 synthetic rubber latex Polymers 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/65—Additives macromolecular
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, 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 an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/16—Homopolymers or copolymers of alkyl-substituted styrenes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/24—Homopolymers or copolymers of amides or imides
- C08L33/26—Homopolymers or copolymers of acrylamide or methacrylamide
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D195/00—Coating compositions based on bituminous materials, e.g. asphalt, tar, pitch
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Paints Or Removers (AREA)
- Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
Abstract
내수성 및 강도 등의 성능이 우수한 방수 도막 형성용 수용성 아스팔트계 방수제가 개시되어 있다. 상기 방수제는 산값이 120 내지 210mgKOH/g이고, 알칼리 용해 가능한 중화된 스티렌/아크릴계 수지와 알킬기를 갖는 단량체와 아세토기를 갖는 단량체 혼합물을 중합한 후, 디아민기를 갖는 물질을 투입하여 제조된 상온 가교형 에멀젼 수지 10 내지 70 중량% 및 유화 아스팔트 30 내지 90 중량%를 포함한다. 이러한 조성을 갖는 방수제는 형성되는 수용성 아스팔트계 방수 도막 내에 가교 성능을 부여함으로써 내부 건조시간이 단축되고 내수성 및 강도 등의 화학적, 물리적 성능이 우수한 방수 도막을 형성시킬 수 있다.A water-soluble asphalt-based waterproofing agent for forming a waterproof coating film having excellent performances such as water resistance and strength is disclosed. The waterproofing agent has an acid value of 120 to 210 mgKOH / g, and polymerizes a monomer mixture having an alkali-soluble neutralized styrene / acrylic resin, a monomer having an alkyl group, and an aceto group, and then adding a substance having a diamine group to prepare a room temperature crosslinking emulsion. 10 to 70% by weight resin and 30 to 90% by weight emulsified asphalt. The waterproofing agent having such a composition provides a crosslinking performance in the water-soluble asphalt-based waterproofing film to be formed, thereby shortening the internal drying time and forming a waterproofing coating having excellent chemical and physical performances such as water resistance and strength.
Description
본 발명은 방수제에 관한 것으로, 더욱 상세하게는 방수 도막을 형성할 수 있는 방수 도막 형성용 수용성 아스팔트계 방수제에 관한 것이다. The present invention relates to a waterproofing agent, and more particularly, to a water-soluble asphalt-based waterproofing agent for forming a waterproofing coating that can form a waterproofing coating.
일반적으로 방수제는 수성 또는 유성의 액상 형태의 방수제를 표면에 도포하여 수분 또는 용제가 증발되고 남은 피막을 이용하여 방수효과를 거두는 조성물을 말한다. 상기 방수제는 일반적으로 건축, 토목 구조물의 외부 방수와, 지하구조물의 옹벽 또는 천정의 방수 및 화장실, 욕실, 베란다 등의 실내 방수를 위해 사용된다. In general, the waterproofing agent refers to a composition in which a waterproofing agent in an aqueous or oily liquid form is applied to a surface to obtain a waterproofing effect using a remaining film after evaporation of water or a solvent. The waterproofing agent is generally used for external waterproofing of construction and civil engineering structures, waterproofing of retaining walls or ceilings of underground structures, and indoor waterproofing of toilets, bathrooms, verandas, and the like.
상기 방수제는 크게 고무화 아스팔트, 아크릴고무 또는 아크릴 수지 등을 주성분으로 하는 에멀젼형과, 클로로프렌 또는 클로로설폰화폴리에틸렌이 함유되어 있고 우레탄 또는 에폭시수지를 주성분으로 하는 반응형으로 구분된다. 이들 중 에멀젼형의 고무화 아스팔트계 방수제와 반응형의 우레탄계 방수제가 주로 사용되고 있다.The waterproofing agent is classified into an emulsion type mainly composed of rubberized asphalt, acrylic rubber or acrylic resin, and a reactive type containing chloroprene or chlorosulfonated polyethylene and having a urethane or epoxy resin as a main component. Among these, emulsion type rubberized asphalt waterproofing agents and reactive urethane waterproofing agents are mainly used.
특히, 상기 고무화 아스팔트계 방수제는 아스팔트에 스티렌 계통의 중합체, 에틸렌-비닐 아세테이트 또는 스티렌-부타디엔 라텍스 중 적어도 하나가 포함되며, 상기 아스팔트가 가지지 못한 우수한 신장율, 내균열성, 내한성 및 접합성 등의 특성을 갖도록 개질시켜 형성된다. 또한, 상기 아스팔트의 내열성과 강도 및 경도를 보다 강화시키기 위해 계면활성제나 경화 촉진제가 첨가되기도 하며, 열가소성 엘라스토머(thermoplastic elastomer)가 첨가되어 형성될 수 있다. In particular, the rubberized asphalt-based waterproofing agent includes at least one of a styrene-based polymer, ethylene-vinyl acetate, or styrene-butadiene latex in the asphalt, and characteristics such as excellent elongation, crack resistance, cold resistance, and bondability that the asphalt does not have It is formed by modifying to have. In addition, a surfactant or a curing accelerator may be added to further enhance the heat resistance, strength, and hardness of the asphalt, and may be formed by adding a thermoplastic elastomer.
이때, 상기 고무화 아스팔트계 방수제는 크게 수용성과 유성으로 분류되는데 유성의 방수제의 경우는 환경 오염의 문제점을 내포하고 있다. 즉, 상기 유성의 고무화 아스팔트계 방수제는 용제로서 톨루엔 등을 포함하고 있는데, 상기 톨루엔은 환경 오염물로서 오염물 처리 문제를 유발한다. 또한, 피도포재 표면에 수분이 잔류하는 경우에 침투력이 약하여 상기 유성의 고무화 아스팔트계 방수제는 접착력이 떨어지는 문제점을 유발한다. At this time, the rubberized asphalt-based waterproofing agent is classified into water-soluble and oily, but the oil-based waterproofing agent has a problem of environmental pollution. That is, the oil-based rubberized asphalt-based waterproofing agent contains toluene, etc. as a solvent, the toluene causes pollution problems as environmental pollutants. In addition, when moisture remains on the surface of the coating material, the penetration force is weak, causing the oily rubberized asphalt-based waterproofing agent to be inferior in adhesive strength.
따라서, 상기 유성의 고무화 아스팔트계 방수제에 비해 환경친화적이며, 피도포재 표면에 수분 함량이 많은 경우에도 시공을 할 수 있는 상기 수용성의 고무화 아스팔트계 방수제가 일반적으로 많이 사용되고 있다.Therefore, the water-soluble rubberized asphalt-based waterproofing agent which is more environmentally friendly than the oil-based rubberized asphalt-based waterproofing agent which can be applied even when the surface of the coated material has a large amount of water is generally used.
상기 수용성의 고무화 아스팔트계 방수제를 이용하여 방수 도막을 형성하기 위해서는 우선, 방수 도막을 형성하고자 하는 장소에 솔, 롤러 또는 스프레이 등을 이용하여 상기 수용성의 고무화 아스팔트계 방수제를 도포시켜 예비 방수 도막을 형성한다. 이어서, 상기 수용성의 고무화 아스팔트계 방수제에 포함되어 있는 수분을 자연 건조시켜 방수 도막을 형성한다. In order to form a waterproof coating using the water-soluble rubberized asphalt-based waterproofing agent, first, by applying a water-soluble rubberized asphalt-based waterproofing agent using a brush, roller or spray to a place where the waterproofing film is to be formed, a preliminary waterproofing film To form. Subsequently, moisture contained in the water-soluble rubberized asphalt waterproofing agent is naturally dried to form a waterproof coating film.
그러나, 상기 방수 도막을 형성하기 위해 수분이 완전히 건조되어 경화가 이 루어지기까지는 대략 24시간이 소요되므로 후속공정 투입이 늦어 공사기간이 지연되는 문제점을 갖는다. 특히, 시공 후 24시간(경화시간)이내에 비를 맞으면 상기 방수제가 물에 용해되어 방수층 파단으로 인한 재시공의 번거로움이 발생된다. 또한, 추운 지역에서는 수분의 증발이 어렵기 때문에 경화가 어려워 상기 수용성의 방수제를 사용하기에 곤란하고, 더운 지역에서는 도포한 상기 방수 도막이 흘러내리기 때문에 일정한 두께를 유지하기 위해서는 2 내지 5회 반복 시공을 필요로 하는 등 온도 조건 및 기후 조건에 따른 문제가 있어 적용하기가 힘든 실정이다.However, it takes about 24 hours until the moisture is completely dried to harden to form the waterproof coating film has a problem that the construction process is delayed because the subsequent process input is late. In particular, when rain falls within 24 hours (curing time) after construction, the waterproofing agent is dissolved in water, causing trouble of re-installation due to breakage of the waterproofing layer. In addition, it is difficult to use the water-soluble waterproofing agent because it is hard to evaporate moisture in a cold region, and in order to maintain a constant thickness, two to five repetitive constructions are performed because the waterproof coating film applied flows down in a hot region. It is difficult to apply because there is a problem depending on the temperature and climate conditions, such as need.
즉, 상기 방수 도막 형성용 수용성 아스팔트계 방수제는 수분 증발 속도에 따라 도막의 건조 속도가 결정되는 열가소성 방수 도막을 형성하기 때문에 특히, 습도가 매우 높거나 기온이 낮은 시공 현장에서 건조 불량이 발생된다. 또한, 상기 방수 도막을 형성하기 위한 표면 또는 내부 건조가 지연되는 경우가 공사 지연에 가장 큰 원인이 되고 있는 실정이다.That is, since the water-soluble asphalt-based waterproofing agent for forming a waterproofing coating film forms a thermoplastic waterproofing coating in which the drying rate of the coating is determined according to the rate of evaporation of water, in particular, poor drying occurs in a construction site having a very high humidity or a low temperature. In addition, the case where the surface or the internal drying for forming the waterproof coating film is delayed is the situation causing the greatest delay in construction.
본 발명의 목적은 내부 건조 시간을 단축시키고 내수성 및 강도가 향상된 방수 도막을 형성할 수 있는 수용성 아스팔트계 방수제를 제공하는 것이다.An object of the present invention is to provide a water-soluble asphalt-based waterproofing agent capable of shortening the internal drying time and forming a waterproof coating with improved water resistance and strength.
상기 목적을 달성하기 위하여 본 발명의 방수 도막 형성용 수용성 아스팔트계 방수제는 산값이 120 내지 210mgKOH/g이고, 알칼리 용해 가능한 중화된 스티렌/아크릴계 수지와 알킬기를 갖는 단량체와 아세토기를 갖는 단량체 혼합물을 중합한 후, 디아민기를 갖는 물질을 투입하여 제조된 상온 가교형 에멀젼 수지 10 내지 70 중량% 및 유화 아스팔트 30 내지 90 중량%를 포함한다.In order to achieve the above object, the water-soluble asphalt waterproofing agent for forming a waterproof coating film of the present invention has an acid value of 120 to 210 mgKOH / g, and polymerized a monomer mixture having an alkali-soluble neutralized styrene / acrylic resin, a monomer having an alkyl group, and an aceto group. After that, 10 to 70 wt% of the room temperature crosslinkable emulsion resin prepared by adding a substance having a diamine group and 30 to 90 wt% of the emulsified asphalt.
일 예로서, 상기 유화 아스팔트는 양이온계 유화 아스팔트, 음이온계 유화 아스팔트 및 비이온계 유화 아스팔트 등을 사용할 수 있다. 특히, 상기 수용성 아스팔트계 방수제는 상기 상온 가교형 에멀젼 수지 20 내지 60 중량% 및 상기 유화 아스팔트 40 내지 80 중량%를 포함할 수 있다.As an example, the emulsified asphalt may be cationic emulsified asphalt, anionic emulsified asphalt, nonionic emulsified asphalt, or the like. In particular, the water-soluble asphalt-based waterproofing agent may include 20 to 60% by weight of the room temperature cross-linked emulsion resin and 40 to 80% by weight of the emulsified asphalt.
상술한 조성을 갖는 수용성 아스팔트계 방수제는 형성되는 방수 도막 내에 상온 가교성 에멀젼 수지가 포함되어 가교 구조를 형성할 수 있으므로 내수성, 바닥과의 점착성 및 강도를 보강시킬 수 있다. 따라서, 내부 건조시간이 단축시킬 수 있는 방수 도막을 형성할 수 있다. 또한 개질된 유화 아스팔트를 첨가함으로써 방수성, 방청성 및 점착성 등의 화학적, 물리적 성능이 우수한 아스팔트계 방수 도막을 형성할 수 있다.The water-soluble asphalt-based waterproofing agent having the above-mentioned composition may include a room temperature crosslinkable emulsion resin in a waterproof coating film to be formed to form a crosslinked structure, thereby reinforcing water resistance, adhesiveness with the bottom, and strength. Therefore, the waterproof coating film which can shorten an internal drying time can be formed. In addition, by adding the modified emulsified asphalt, it is possible to form an asphalt-based waterproof coating film having excellent chemical and physical performances such as water resistance, rust resistance and adhesion.
이하, 본 발명의 방수 도막 형성용 수용성 아스팔트계 방수제에 대하여 상세히 설명하기로 한다.Hereinafter, the water-soluble asphalt-based waterproofing agent for forming a waterproof coating film of the present invention will be described in detail.
본 발명의 방수 도막 형성용 수용성 아스팔트계 방수제는 상온 가교형 에멀젼 수지 및 유화 아스팔트(emulsified asphalt)를 포함하는 조성을 갖는다.The water-soluble asphalt-based waterproofing agent for forming a waterproof coating film of the present invention has a composition including a room temperature cross-linkable emulsion resin and emulsified asphalt.
상기 수용성 아스팔트계 방수제를 형성하기 위해 적용되는 상기 상온 가교형 에멀젼 수지는 산값이 190 내지 210mgKOH/g 범위를 갖는 스티렌/아크릴계 알칼리에 용해가능한 수지를 중화제로 중화시키고, 단량체와 아세토기를 갖는 단량체 혼합물을 중합한 후, 디아민기를 갖는 물질을 첨가하여 제조한다.The room temperature crosslinkable emulsion resin applied to form the water-soluble asphalt-based waterproofing agent neutralizes a resin soluble in a styrene / acrylic alkali having an acid value in the range of 190 to 210 mgKOH / g with a neutralizing agent and a monomer mixture having a monomer and an aceto group. After the polymerization, a substance having a diamine group is added to prepare it.
상기 스티렌/아크릴계 수지의 사용량이 10 중량% 미만일 경우 에멀젼 수지의 입자경이 커지면서 에멀젼 입자간 안정성이 떨어진다. 반면에 그 사용량이 40 중량%를 초과할 경우 에멀젼 수지의 입자경이 작아지면서 점도와 산값이 높아져 내수성 및 내알칼리성이 취약해진다. 따라서, 상기 스티렌/아크릴계 수지는 상기 알킬기를 갖는 단량체 전체 중량의 약 10 내지 40 중량%를 사용하는 것이 바람직하다. 상기 스티렌/아크릴계 알칼리에 용해가능한 수지의 구체적인 예로서는 J.C. Johnson 사의 산값이 200인 Joncryl-67을 들 수 있다. When the amount of the styrene / acrylic resin is less than 10% by weight, the particle size of the emulsion resin is increased while the stability between emulsion particles is poor. On the other hand, when the amount of use exceeds 40% by weight, the particle size of the emulsion resin is reduced, the viscosity and acid value is increased, so that the water resistance and alkali resistance is weak. Therefore, the styrene / acrylic resin preferably uses about 10 to 40% by weight of the total weight of the monomer having an alkyl group. Specific examples of the resin soluble in the styrene / acrylic alkali include J.C. Joncryl-67, which has an acid value of 200, is available from Johnson.
또한, 상기 스티렌/아크릴계 수지를 중화시키기 위해 사용되는 상기 중화제의 예로서는 암모니아 수용액, 수산화나트륨 등을 들 수 있다. In addition, examples of the neutralizing agent used for neutralizing the styrene / acrylic resin include aqueous ammonia solution, sodium hydroxide and the like.
상기 중합에 사용되는 상기 단량체 혼합물에는 아세토기를 갖는 단량체와 알킬기를 갖는 단량체를 포함한다. 상기 아세토기를 갖는 단량체의 예로서는 디아세톤아크릴아마이드, 아세토아세톡시아크릴레이트 및 아세토아세톡시에틸 메타아크릴레이트 등을 들 수 있으며, 단독으로 또는 2종 이상을 혼합하여 사용할 수 있다. The monomer mixture used for the polymerization includes a monomer having an aceto group and a monomer having an alkyl group. Examples of the monomer having an aceto group include diacetone acrylamide, acetoacetoxy acrylate, acetoacetoxyethyl methacrylate, and the like, and may be used alone or in combination of two or more thereof.
또한, 상기 알킬기를 갖는 단량체의 예로서는 메틸메타아크릴레이트, 에틸메타아크릴레이트, 프로필메타아크릴레이트, 부틸메타아크릴레이트, 2-에틸헥실메타아크릴레이트, 부틸아크릴레이트, 스티렌, 메타아크릴산에스테르, 에틸아크릴산에스테르 및 부틸아크릴산에스테르 등을 들 수 있으며, 마찬가지로 단독으로 또는 2종 이상의 혼합물로서 사용된다. In addition, examples of the monomer having an alkyl group include methyl methacrylate, ethyl methacrylate, propyl methacrylate, butyl methacrylate, 2-ethylhexyl methacrylate, butyl acrylate, styrene, methacrylic acid ester, and ethyl acrylate ester. And butyl acrylate ester etc. are mentioned, It is similarly used individually or as a mixture of 2 or more types.
이때, 상기 아세토기를 갖는 단량체의 첨가량이 0.1 중량% 미만일 경우 가교 구조가 잘 일어나지 못하고, 10 중량%를 초과하면 중합시 미반응 잔류량이 많아지 며 상기 미반응 잔류량이 이후 개시제와 만나 티를 형성시켜 수지의 외관이 불량해진다. 따라서, 상기 아세토기를 갖는 단량체의 사용량은 상기 알킬기를 갖는 단량체의 사용량의 약 0.1 내지 10 중량%를 사용하는 것이 바람직하다. 여기에 중합개시제가 첨가될 수 있으며, 사용되는 중합개시제는 일예로서 과황산암모늄, 과황산칼륨 등을 들 수 있다. 상기 중합개시제의 첨가량은 상기 알킬기를 갖는 단량체에 대해 0.05 내지 3 중량%까지 사용된다.At this time, when the amount of the monomer having an aceto group is less than 0.1% by weight, the crosslinking structure does not occur well. When the amount of the monomer having an aceto group exceeds 10% by weight, the amount of unreacted residue during polymerization increases, and the unreacted residue subsequently forms a tee with an initiator. The appearance of the resin becomes poor. Therefore, the amount of the monomer having an aceto group is preferably used from about 0.1 to 10% by weight of the amount of the monomer having an alkyl group. A polymerization initiator may be added thereto, and the polymerization initiator used may include, for example, ammonium persulfate, potassium persulfate, and the like. The addition amount of the polymerization initiator is used up to 0.05 to 3% by weight based on the monomer having an alkyl group.
그리고, 상기 디아민기를 갖는 물질은 에틸렌디아민, 헥사메틸렌디아민, 히드라진 및 아디픽디하이드라자이드 등을 사용할 수 있다. 상기 디아민기를 갖는 물질을 첨가하면 상온에서 수분의 증발과 더불어 에멀젼 입자에 있는 아세토기가 케토-에놀 토토머리즘을 통해 에놀형으로 전환된다. 이때, 상기 에놀형으로 전환된 아세토기의 두 분자가 디아민기를 갖는 물질의 한 분자와 반응하여 물 두 분자가 빠져나가면서 에나민 가교 결합을 이룬다. 따라서 상기 방수 도막 형성용 수용성 아스팔트계 방수제로 형성한 방수 도막에 가교 성능을 부여하게 된다.As the material having the diamine group, ethylenediamine, hexamethylenediamine, hydrazine, adipic dihydrazide, and the like may be used. The addition of the material having the diamine group converts the aceto groups in the emulsion particles into the enol form through keto-enol totomism with the evaporation of water at room temperature. At this time, two molecules of the aceto group converted to the enol form react with one molecule of a substance having a diamine group, thereby forming two molecules of water to form an enamine crosslink. Therefore, the crosslinking performance is imparted to the waterproof coating film formed of the water-soluble asphalt-based waterproofing agent for forming the waterproof coating film.
여기서, 상기 형성하고자 하는 방수제에 포함된 상온 가교형 에멀젼 수지의 함량이 10 중량% 미만일 경우 기존의 아스팔트계 방수 도막에 부여되는 가교 성능이 저하된다. 반면에, 그 함량이 70 중량%를 초과할 경우 아스팔트의 연성, 방수, 방청 및 접착 성능이 현저히 떨어지고, 경제적으로도 효과를 얻을 수 없다. Here, when the content of the room temperature cross-linked emulsion resin contained in the waterproofing agent to be formed is less than 10% by weight, the crosslinking performance imparted to the existing asphalt-based waterproof coating is lowered. On the other hand, when the content exceeds 70% by weight, the ductility, waterproofing, rust prevention and adhesion performance of the asphalt is significantly reduced, and economically ineffective.
따라서, 상기 수용성 아스팔트계 방수제는 상온 가교형 에멀젼 수지를 10 내지 70 중량% 포함하고, 바람직하게는 20 내지 60 중량%의 함량을 포함한다.Therefore, the water-soluble asphalt-based waterproofing agent contains 10 to 70 wt% of the room temperature crosslinkable emulsion resin, and preferably contains 20 to 60 wt%.
상기 유화 아스팔트의 예로서는 상기 유화제가 양전하를 띠고 있는 양이온계 유화 아스팔트, 음전하를 띠고 있는 음이온계 유화 아스팔트 및 양/음전하 중 어느 전하도 갖지 않는 비이온계 유화 아스팔트 등을 들 수 있다. 또한, 상기 유화 아스팔트를 합성고무 라텍스와 천연고무 라텍스 등으로 개질시킨 양이온계, 음이온계 및 비이온계 유화 아스팔트 등도 사용할 수 있다. Examples of the emulsified asphalt include cationic emulsified asphalt in which the emulsifier has a positive charge, anionic emulsified asphalt in a negative charge, and nonionic emulsified asphalt having neither of positive or negative charges. In addition, cationic, anionic and nonionic emulsified asphalt may be used in which the emulsified asphalt is modified with synthetic rubber latex and natural rubber latex.
상기 형성하고자 하는 방수제를 형성하기 위해 적용되는 상기 유화 아스팔트의 함량이 30 중량% 미만일 경우에 아스팔트의 연성, 방수, 방청 및 점착 성능이 현저히 떨어진다. 반면에, 상기 유화 아스팔트의 함량이 90 중량%를 초과할 경우 기계적 강도 등의 물리적 성능이 현저히 감소된다. When the content of the emulsified asphalt applied to form the waterproofing agent to be formed is less than 30% by weight, the ductility, waterproofing, rustproofing and adhesion performance of the asphalt are significantly reduced. On the other hand, when the content of the emulsified asphalt exceeds 90% by weight, physical performance such as mechanical strength is significantly reduced.
따라서, 상기 수용성 아스팔트계 방수제는 상기 유화 아스팔트를 30 내지 90 중량% 포함하고, 바람직하게는 40 내지 80 중량%의 함량을 포함한다. Therefore, the water-soluble asphalt-based waterproofing agent contains 30 to 90% by weight of the emulsified asphalt, and preferably contains a content of 40 to 80% by weight.
이하, 본 발명의 구체적인 실시예 및 평가예를 통하여 수용성 아스팔트계 방수제를 상세히 설명하기로 한다. 그러나, 본 발명은 하기의 실시예 및 평가예로 한정되는 것은 아니다. Hereinafter, the water-soluble asphalt-based waterproofing agent will be described in detail through specific examples and evaluation examples of the present invention. However, the present invention is not limited to the following examples and evaluation examples.
실시예Example
2L 플라스크에 이온 교환수 487.7g, Joncryl-67 120g, 중화제인 암모니아 수용액 10.3g을 투입한 후 60℃로 승온 유지하면서 Joncryl-67을 용해시켰다. 완전히 용해된 것을 확인하고 80℃로 승온한 후, 중합개시제인 과황산암모늄 1g을 이온교환수 10g에 녹여 투입하였다. 이후, 스티렌 모노머 150g과 n-부틸아크릴레이트 50g 의 단량체 혼합액을 2시간 동안 적하하였다. 이어서, 스티렌 모노머 50g, n-부틸아크릴레이트 90g, 메틸메타아크릴레이트 60g, 디아세톤아크릴아마이드 4g의 단량체 혼합물과 과황산암모늄 1g을 이온교환수 100g에 녹인 수용액을 동시에 3시간 동안 적하하였다. 적하 종료 후, 반응을 1시간 동안 유지한 후 50℃ 이하로 냉각하고, 암모니아 수용액 5g, 디아민기를 갖는 아디픽디하이드라자이드 2g을 이온교환수 13g에 녹여 투입하여 상온 가교성 에멀젼 수지를 합성하였다.487.7 g of ion-exchanged water, 120 g of Joncryl-67, and 10.3 g of an aqueous ammonia solution were added to the 2 L flask, and Joncryl-67 was dissolved while maintaining the temperature at 60 ° C. After confirming that the solution was completely dissolved, the temperature was raised to 80 ° C, and 1 g of ammonium persulfate as a polymerization initiator was dissolved in 10 g of ion-exchange water. Thereafter, a monomer mixture of 150 g of styrene monomer and 50 g of n-butylacrylate was added dropwise for 2 hours. Subsequently, a monomer mixture of 50 g of styrene monomer, 90 g of n-butyl acrylate, 60 g of methyl methacrylate, and 4 g of diacetone acrylamide and an aqueous solution of 1 g of ammonium persulfate dissolved in 100 g of ion-exchanged water were simultaneously added dropwise for 3 hours. After completion of the dropwise addition, the reaction was maintained for 1 hour and then cooled to 50 ° C. or less, 5 g of ammonia aqueous solution and 2 g of adipic dihydrazide having a diamine group were dissolved in 13 g of ion-exchanged water to synthesize a room temperature crosslinkable emulsion resin.
1L 플라스크에 유화 아스팔트 300g를 투입하고 교반기를 이용하여 교반하면서 상기 합성한 상온 가교성 에멀젼 수지 200g를 천천히 투입시켜 수용성 아스팔트계 방수제를 수득하였다.300 g of emulsified asphalt was added to a 1 L flask and 200 g of the synthesized room temperature crosslinkable emulsion resin was slowly added while stirring using a stirrer to obtain a water-soluble asphalt waterproofing agent.
수용성 아스팔트계 방수제의 방수 도막 평가Evaluation of Waterproofing Film of Water Soluble Asphalt Waterproofing Agent
상기 실시예에 의해 제조된 수용성 아스팔트계 방수제 및 유화 아스팔트를 각각 슬레이트 판에 0.01 내지 2mm의 두께로 도장하여 방수 도막을 얻었다. 또한, 각각의 방수 도막 시편에 대해 건조 시간을 측정하였다. 그 결과는 하기 표 1에 개시되어 있다. The water-soluble asphalt-based waterproofing agent and the emulsified asphalt prepared in the above Examples were respectively coated on a slate plate to a thickness of 0.01 to 2 mm to obtain a waterproof coating film. In addition, drying time was measured for each waterproof coating film specimen. The results are shown in Table 1 below.
[표 1]TABLE 1
상기 표 1을 참조하면, 상기 실시예의 건조시간 평가 결과에서 알 수 있듯이 수득된 수용성 아스팔트계 방수제는 기존 유화 아스팔트만을 사용하여 방수 도막을 형성한 후 건조할 때에 비해 건조시간이 약 2배 이상으로 감소되는 효과를 가졌다. 이는 에멀젼 수지를 혼합함으로써 에멀젼 수지의 가교 구조 형성이 건조시간을 단축시키는 효과를 가져온 것으로 보인다. Referring to Table 1, as can be seen from the drying time evaluation results of the embodiment, the obtained water-soluble asphalt-based waterproofing agent reduced the drying time by about two times or more compared with drying after forming a waterproof coating film using only conventional emulsified asphalt. Had the effect of. This seems to result in the formation of the crosslinked structure of the emulsion resin by shortening the drying time by mixing the emulsion resin.
상술한 조성을 갖는 수용성 아스팔트계 방수제는 형성되는 방수 도막 내에 상온 가교성 에멀젼 수지가 포함되어 가교 구조를 형성할 수 있으므로 내수성, 바닥과의 점착성 및 강도를 보강시킬 수 있다. 따라서, 내부 건조시간이 단축시킬 수 있는 방수 도막을 형성할 수 있다. 또한 개질된 유화 아스팔트를 첨가함으로써 방수성, 방청성 및 점착성 등의 화학적, 물리적 성능이 우수한 아스팔트계 방수 도막을 형성할 수 있다.The water-soluble asphalt-based waterproofing agent having the above-mentioned composition may include a room temperature crosslinkable emulsion resin in a waterproof coating film to be formed to form a crosslinked structure, thereby reinforcing water resistance, adhesiveness with the bottom, and strength. Therefore, the waterproof coating film which can shorten an internal drying time can be formed. In addition, by adding the modified emulsified asphalt, it is possible to form an asphalt-based waterproof coating film having excellent chemical and physical performances such as water resistance, rust resistance and adhesion.
이와 같이, 건축토목 공사에 있어서 기존에 사용하고 있던 방수 도막 형성용 수용성 아스팔트계 방수제가 안고 있는 매우 느린 내부 건조시간으로 인한 공사기간 지연 문제점과 수용성의 열가소성 도막의 물리적 성능이 취약한 문제점을 동시에 해결할 수 있어 실내용 및 건축용 방수 시공을 빠르고 효과적으로 수행할 수 있다.As such, it is possible to solve the problem of delay in the construction period due to the very slow internal drying time of the water-soluble asphalt-based waterproofing agent used in the construction civil engineering and the physical performance of the water-soluble thermoplastic coating at the same time. It can be performed quickly and effectively for indoor and construction waterproofing.
이상, 본 발명의 바람직한 실시예를 참조하여 설명하였지만 해당 기술분야의 숙련된 당업자라면 하기의 특허 청구의 범위에 기재된 본 발명의 사상 및 영역으로부터 벗어나지 않는 범위 내에서 본 발명을 다양하게 수정 및 변경시킬 수 있 음을 이해할 수 있을 것이다. Although the above has been described with reference to the preferred embodiments of the present invention, those skilled in the art can variously modify and change the present invention without departing from the spirit and scope of the present invention as set forth in the claims below. I can understand that you can.
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
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CN106010253A (en) * | 2016-06-24 | 2016-10-12 | 衡水中铁建土工材料制造有限公司 | Waterproof double-component rubber spray coating realizing rapid hardening and preparation method of coating |
KR20200094347A (en) | 2019-01-30 | 2020-08-07 | 주식회사 신영기업 | Water soluble elastic insulation waterproof agent and method for pavement marking using the same |
KR102161202B1 (en) | 2020-04-29 | 2020-10-05 | (주) 세원방수 | Composition and Method of water proofing material for reaction curing waterborne-rubber asphalt |
CN116574424A (en) * | 2023-05-10 | 2023-08-11 | 广东衡光新材料科技有限公司 | A special emulsion for water-based asphalt-based waterproof coating and its preparation method and application |
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KR20010099040A (en) * | 2001-08-16 | 2001-11-09 | 정인규 | Compisition of flooring agent for wateborn-rubber asphalt moltar |
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KR20010099040A (en) * | 2001-08-16 | 2001-11-09 | 정인규 | Compisition of flooring agent for wateborn-rubber asphalt moltar |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
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CN106010253A (en) * | 2016-06-24 | 2016-10-12 | 衡水中铁建土工材料制造有限公司 | Waterproof double-component rubber spray coating realizing rapid hardening and preparation method of coating |
KR20200094347A (en) | 2019-01-30 | 2020-08-07 | 주식회사 신영기업 | Water soluble elastic insulation waterproof agent and method for pavement marking using the same |
KR102161202B1 (en) | 2020-04-29 | 2020-10-05 | (주) 세원방수 | Composition and Method of water proofing material for reaction curing waterborne-rubber asphalt |
CN116574424A (en) * | 2023-05-10 | 2023-08-11 | 广东衡光新材料科技有限公司 | A special emulsion for water-based asphalt-based waterproof coating and its preparation method and application |
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