JP4561115B2 - Polymer cement composition and concrete structure thereof - Google Patents
Polymer cement composition and concrete structure thereof Download PDFInfo
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- JP4561115B2 JP4561115B2 JP2004032133A JP2004032133A JP4561115B2 JP 4561115 B2 JP4561115 B2 JP 4561115B2 JP 2004032133 A JP2004032133 A JP 2004032133A JP 2004032133 A JP2004032133 A JP 2004032133A JP 4561115 B2 JP4561115 B2 JP 4561115B2
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- 239000000203 mixture Substances 0.000 title claims description 105
- 239000011414 polymer cement Substances 0.000 title claims description 86
- 239000000839 emulsion Substances 0.000 claims description 138
- 239000004568 cement Substances 0.000 claims description 44
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 32
- 230000009477 glass transition Effects 0.000 claims description 22
- 239000000463 material Substances 0.000 claims description 22
- 239000007787 solid Substances 0.000 claims description 20
- 239000000945 filler Substances 0.000 claims description 13
- 229910052808 lithium carbonate Inorganic materials 0.000 claims description 10
- 238000004078 waterproofing Methods 0.000 claims description 10
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 claims description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 5
- 239000004908 Emulsion polymer Substances 0.000 claims 1
- 239000010410 layer Substances 0.000 description 43
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 27
- 239000005038 ethylene vinyl acetate Substances 0.000 description 23
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 23
- 229920000642 polymer Polymers 0.000 description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 23
- 239000004925 Acrylic resin Substances 0.000 description 19
- 229920000178 Acrylic resin Polymers 0.000 description 19
- 239000011248 coating agent Substances 0.000 description 15
- 238000000576 coating method Methods 0.000 description 15
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 14
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 12
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 10
- 239000000725 suspension Substances 0.000 description 10
- 239000000454 talc Substances 0.000 description 10
- 229910052623 talc Inorganic materials 0.000 description 10
- 239000004576 sand Substances 0.000 description 9
- 239000000377 silicon dioxide Substances 0.000 description 9
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 8
- 239000000178 monomer Substances 0.000 description 8
- 239000001993 wax Substances 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 229920003002 synthetic resin Polymers 0.000 description 7
- 239000000057 synthetic resin Substances 0.000 description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 239000000084 colloidal system Substances 0.000 description 6
- 238000010276 construction Methods 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 230000001681 protective effect Effects 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 5
- 239000005977 Ethylene Substances 0.000 description 5
- 239000004372 Polyvinyl alcohol Substances 0.000 description 5
- 239000002518 antifoaming agent Substances 0.000 description 5
- 239000003995 emulsifying agent Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 229920002451 polyvinyl alcohol Polymers 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- -1 2-ethylhexyl Chemical group 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 238000007429 general method Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000004570 mortar (masonry) Substances 0.000 description 4
- 239000012188 paraffin wax Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000010454 slate Substances 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 239000003638 chemical reducing agent Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229910003002 lithium salt Inorganic materials 0.000 description 3
- 159000000002 lithium salts Chemical class 0.000 description 3
- 239000002736 nonionic surfactant Substances 0.000 description 3
- 239000003505 polymerization initiator Substances 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- IIPYXGDZVMZOAP-UHFFFAOYSA-N lithium nitrate Chemical compound [Li+].[O-][N+]([O-])=O IIPYXGDZVMZOAP-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000002893 slag Substances 0.000 description 2
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 2
- 229920003169 water-soluble polymer Polymers 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- XFWJKVMFIVXPKK-UHFFFAOYSA-N calcium;oxido(oxo)alumane Chemical group [Ca+2].[O-][Al]=O.[O-][Al]=O XFWJKVMFIVXPKK-UHFFFAOYSA-N 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- JCCYXJAEFHYHPP-OLXYHTOASA-L dilithium;(2r,3r)-2,3-dihydroxybutanedioate Chemical compound [Li+].[Li+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O JCCYXJAEFHYHPP-OLXYHTOASA-L 0.000 description 1
- JHFZWTMEVGPUTE-UHFFFAOYSA-L dilithium;2-hydroxybutanedioate Chemical compound [Li+].[Li+].[O-]C(=O)C(O)CC([O-])=O JHFZWTMEVGPUTE-UHFFFAOYSA-L 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- XIXADJRWDQXREU-UHFFFAOYSA-M lithium acetate Chemical compound [Li+].CC([O-])=O XIXADJRWDQXREU-UHFFFAOYSA-M 0.000 description 1
- 229940071264 lithium citrate Drugs 0.000 description 1
- WJSIUCDMWSDDCE-UHFFFAOYSA-K lithium citrate (anhydrous) Chemical compound [Li+].[Li+].[Li+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O WJSIUCDMWSDDCE-UHFFFAOYSA-K 0.000 description 1
- INHCSSUBVCNVSK-UHFFFAOYSA-L lithium sulfate Inorganic materials [Li+].[Li+].[O-]S([O-])(=O)=O INHCSSUBVCNVSK-UHFFFAOYSA-L 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000001451 organic peroxides Chemical class 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
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000004968 peroxymonosulfuric acids Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910021487 silica fume Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 235000010262 sodium metabisulphite Nutrition 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- RBTVSNLYYIMMKS-UHFFFAOYSA-N tert-butyl 3-aminoazetidine-1-carboxylate;hydrochloride Chemical compound Cl.CC(C)(C)OC(=O)N1CC(N)C1 RBTVSNLYYIMMKS-UHFFFAOYSA-N 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Landscapes
- Curing Cements, Concrete, And Artificial Stone (AREA)
Description
本発明は、コンクリート構造物などに施工して、防水性を付与する硬化物を得ることができる防水性のポリマーセメント組成物及びそのポリマーセメント組成物の硬化物層を有するコンクリート構造体に関する。 The present invention relates to a waterproof polymer cement composition that can be applied to a concrete structure or the like to obtain a cured product that imparts waterproof properties, and a concrete structure having a cured product layer of the polymer cement composition.
コンクリート構造物の屋上、地下、ベランダなどに防水性を付与するため、樹脂エマルジョンなどにセメントを配合したポリマーセメント組成物が施工されている。 In order to provide waterproof properties to rooftops, basements, and verandas of concrete structures, a polymer cement composition in which cement is blended with a resin emulsion or the like is applied.
例えば、特許文献1には、炭素数4〜10のアルキル基を有するアルキル(メタ)アクリレートから選ばれた1種以上の単量体30〜98重量%、(メタ)アクリル酸0.1〜3重量%及びグリシジル(メタ)アクリレート0.1〜5重量%を必須構成単量体とし、かつガラス転移温度が−20℃以下である重合体がカチオン性又はノニオン性の界面活性剤により水に乳化分散されているエマルションと、無機質水硬性物質からなることを特徴とする防水材組成物が開示されている。 For example, Patent Document 1 discloses 30 to 98% by weight of one or more monomers selected from alkyl (meth) acrylates having an alkyl group having 4 to 10 carbon atoms, and 0.1 to 3 (meth) acrylic acid. A polymer having an essential constituent monomer of 0.1% by weight and glycidyl (meth) acrylate and having a glass transition temperature of −20 ° C. or lower is emulsified in water by a cationic or nonionic surfactant. There is disclosed a waterproof material composition comprising a dispersed emulsion and an inorganic hydraulic substance.
特許文献2には、ポリマー成分、セメント、骨材、減水剤及び保水剤の各成分を含有し、該ポリマー成分はガラス転移温度(Tg)が−5℃以下で、かつ−20℃を超えるアニオン−カチオン両性アルカリ硬化型アクリル−スチレン系合成樹脂エマルションからなり、セメントに対する該エマルションの樹脂固形分の重量%(P/C)は30〜80%であり、ポゾラン反応を起こす成分としてのシリカフューム微粒子(SiO2含有量が90%以上で、平均粒子径が0.1〜0.2μm)をセメントに対して5〜20%含有することを特徴とするコンクリート防水用組成物が開示されている。 Patent Document 2 contains a polymer component, a cement, an aggregate, a water reducing agent, and a water retention agent. The polymer component has an anion having a glass transition temperature (Tg) of −5 ° C. or lower and exceeding −20 ° C. -It consists of a cationic amphoteric alkali curable acrylic-styrene synthetic resin emulsion, and the weight percentage (P / C) of the resin solid content of the emulsion with respect to cement is 30 to 80%. Silica fume fine particles as a component that causes a pozzolanic reaction ( A concrete waterproofing composition is disclosed, which contains SiO 2 content of 90% or more and an average particle size of 0.1 to 0.2 μm) with respect to cement.
特許文献3には、建造物の表面に、下塗材として下記組成物(1)を施工した後、その塗膜表面上に防水材として下記組成物(2)を施工することを特徴とする湿潤面用防水工法が開示されている。
(1)全固形分を基準にして、1〜50重量%のエポキシ樹脂と5〜99重量%のセメントを含有し、かつこれらの合計量が40重量%以上である組成物。
(2)炭素数4〜10のアルキル基を有するアルキル(メタ)アクリレートから選ばれる1種以上の単量体、(メタ)アクリル酸及びグリシジル(メタ)アクリレートを必須構成単量体とし、かつガラス転移点は−20℃以下である重合体が、界面活性剤により水に乳化分散されているエマルションと、無機質水硬性物質とからなる組成物。
Patent Document 3 discloses that the following composition (1) is applied as a primer to the surface of a building, and then the following composition (2) is applied as a waterproof material to the coating surface. A waterproofing method for a surface is disclosed.
(1) A composition containing 1 to 50% by weight of an epoxy resin and 5 to 99% by weight of cement, based on the total solid content, and the total amount of which is 40% by weight or more.
(2) One or more monomers selected from alkyl (meth) acrylates having an alkyl group having 4 to 10 carbon atoms, (meth) acrylic acid and glycidyl (meth) acrylate as essential constituent monomers, and glass A composition comprising an emulsion in which a polymer having a transition point of −20 ° C. or lower is emulsified and dispersed in water by a surfactant, and an inorganic hydraulic substance.
特許文献4には、建造物の表面に下記(1)からなる下塗材を施工し、その塗膜表面上に下記(2)からなる防水材を施工する防水施工法が開示されている。
(1)特定のアルキル(メタ)アクリレート、メチルアクリレート又はエチルアクリレート及び(メタ)アクリル酸を必須構成単量体とする重合体のエマルションと、無機質水硬性物質からなる組成物。
(2)特定のアルキル(メタ)アクリレート、メチル(メタ)アクリレート及びN−メチロール(メタ)アクリルアミド又はN−アルコキシメチル(メタ)アクリルアミドを必須構成単量体とし、かつTg点が−20℃以下である重合体のエマルションと、無機質水硬性物質からなる組成物。
Patent Document 4 discloses a waterproof construction method in which a primer material composed of the following (1) is applied on the surface of a building, and a waterproof material composed of the following (2) is applied on the surface of the coating film.
(1) A composition comprising a polymer emulsion containing a specific alkyl (meth) acrylate, methyl acrylate or ethyl acrylate and (meth) acrylic acid as essential constituent monomers, and an inorganic hydraulic substance.
(2) A specific alkyl (meth) acrylate, methyl (meth) acrylate and N-methylol (meth) acrylamide or N-alkoxymethyl (meth) acrylamide is an essential constituent monomer, and the Tg point is −20 ° C. or lower. A composition comprising an emulsion of a polymer and an inorganic hydraulic substance.
コンクリート防水用にポリマーを含有するセメント組成物が用いられている。ポリマーを含有するセメント組成物をコンクリート構造体上に被覆し、硬化させて防水層を形成させる時に、コンクリートとセメント組成物の防水層の間にふくれが発生する場合があり、その抑制がもとめられている。 Cement compositions containing polymers have been used for waterproofing concrete. When a cement composition containing a polymer is coated on a concrete structure and cured to form a waterproof layer, blistering may occur between the concrete and the waterproof layer of the cement composition. ing.
本発明は、エマルジョン系のポリマー成分とアルミナセメントとを含むセメント組成物を、コンクリート構造物に施工し、コンクリートとセメント組成物の硬化層との間にふくれの発生を改善した耐水性及び施工性に優れるポリマーエマルジョン系の防水層を形成用のポリマーセメント組成物の提供を目的とする。 The present invention relates to water resistance and workability in which a cement composition containing an emulsion-based polymer component and alumina cement is applied to a concrete structure, and blistering is improved between the concrete and the hardened layer of the cement composition. It is an object of the present invention to provide a polymer cement composition for forming a water-resistant layer of a polymer emulsion system that is excellent in water resistance.
本発明の第一は、アルミナセメントと、エマルジョン及び硬化促進剤を含むことを特徴とするポリマーセメント組成物を提供することである。 The first of the present invention is to provide a polymer cement composition comprising an alumina cement, an emulsion and a hardening accelerator.
本発明の第二は、コンクリート層に、ポリマーセメント組成物の硬化物層を積層したコンクリート構造体であり、
ポリマーセメント組成物が本発明の第一に記載のポリマーセメント組成物であることを特徴とするコンクリート構造体を提供することである。
2nd of this invention is the concrete structure which laminated | stacked the hardened | cured material layer of the polymer cement composition on the concrete layer,
It is to provide a concrete structure characterized in that the polymer cement composition is the polymer cement composition according to the first aspect of the present invention.
本発明の第三は、コンクリート層に、プライマーの硬化物層、ポリマーセメント組成物の硬化物層の順に積層したコンクリート構造体であり、
ポリマーセメント組成物が本発明の第一に記載のポリマーセメント組成物であり、
プライマーがエマルジョンであることを特徴とするコンクリート構造体を提供することである。
The third aspect of the present invention is a concrete structure in which a hardened material layer of a primer and a hardened material layer of a polymer cement composition are laminated in this order on a concrete layer,
The polymer cement composition is the polymer cement composition according to the first aspect of the present invention,
It is to provide a concrete structure characterized in that the primer is an emulsion.
本発明の第一、第二又は第三の好ましい態様を以下に示す。
ポリマーセメント組成物は、エマルジョンの固形分100質量部に対し、アルミナセメントを3〜175質量部含むことが好ましい。
ポリマーセメント組成物は、アルミナセメント100質量部に対し、硬化促進剤を0.1〜7質量部含むことが好ましい。
ポリマーセメント組成物は、エマルジョンの固形分100質量部に対し、アルミナセメントを3〜175質量部含み、アルミナセメント100質量部に対し、硬化促進剤を1〜7質量部含むことが好ましい。
ポリマーセメント組成物は、エマルジョンがガラス転移温度0℃以下のエマルジョンを含むことが好ましい。
ポリマーセメント組成物は、エマルジョンが、エチレン−酢酸ビニル系エマルジョン及びアクリル系エマルジョンから選択される1以上のガラス転移温度が0℃以下のエマルジョンを含むことが好ましい。
ポリマーセメント組成物は、さらに充填材を含み、エマルジョンの固形分100質量部に対し、アルミナセメント3〜175質量部含み、かつアルミナセメントと充填材の合計量20〜350質量部を含むことが好ましい。
ポリマーセメント組成物は、コンクリート防水用であることが好ましい。
ポリマーセメント組成物は、防水用ポリマーセメント組成物であることが好ましい。
ポリマーセメント組成物は、ポリマーセメント組成物の可使時間が、0.25時間以上であることが好ましい。
硬化促進剤は、炭酸リチウムを含むことが好ましい。
充填材は珪砂及び/又はタルクを含むことが好ましい。
The 1st, 2nd or 3rd preferable aspect of this invention is shown below.
The polymer cement composition preferably contains 3 to 175 parts by mass of alumina cement with respect to 100 parts by mass of the solid content of the emulsion.
It is preferable that a polymer cement composition contains 0.1-7 mass parts of hardening accelerators with respect to 100 mass parts of alumina cement.
The polymer cement composition preferably contains 3 to 175 parts by mass of alumina cement with respect to 100 parts by mass of the solid content of the emulsion, and 1 to 7 parts by mass of a hardening accelerator with respect to 100 parts by mass of the alumina cement.
In the polymer cement composition, the emulsion preferably contains an emulsion having a glass transition temperature of 0 ° C. or lower.
In the polymer cement composition, the emulsion preferably contains one or more emulsions having a glass transition temperature of 0 ° C. or lower selected from ethylene-vinyl acetate emulsions and acrylic emulsions.
The polymer cement composition further contains a filler, preferably 3 to 175 parts by mass of alumina cement and 20 to 350 parts by mass of the total amount of the alumina cement and filler with respect to 100 parts by mass of the solid content of the emulsion. .
The polymer cement composition is preferably for concrete waterproofing.
The polymer cement composition is preferably a waterproof polymer cement composition.
In the polymer cement composition, the pot life of the polymer cement composition is preferably 0.25 hours or more.
The curing accelerator preferably contains lithium carbonate.
The filler preferably contains silica sand and / or talc.
本発明のポリマーセメント組成物は、施工後の乾燥時間の短い組成物であり、施工するコンクリート構造体とポリマーセメント組成物の硬化物の層との間のふくれの発生を抑制又はなくすことが出来、美観に優れる構造体を得ることが出来る。
本発明のポリマーセメント組成物は、施工性に優れているだけでなく、塗膜特性に優れた防水層を与える。従って、コンクリート構造物への長期防水性付与においてその利用価値は高い。
本発明のコンクリート構造体は、本発明のポリマーセメント組成物の硬化物層を表面に有するため、美観に優れ、防水性などに優れた構造体である。
The polymer cement composition of the present invention is a composition with a short drying time after construction, and can suppress or eliminate the occurrence of blistering between the concrete structure to be constructed and the cured layer of the polymer cement composition. A structure with excellent aesthetics can be obtained.
The polymer cement composition of the present invention is not only excellent in workability but also provides a waterproof layer excellent in coating film characteristics. Therefore, the utility value is high in providing long-term waterproofing to a concrete structure.
Since the concrete structure of the present invention has the cured product layer of the polymer cement composition of the present invention on the surface, the concrete structure is excellent in aesthetics and excellent in waterproofness.
本発明のポリマーセメント組成物は、アルミナセメントと、エマルジョン及び硬化促進剤を含むものであり、さらに充填材などを含むことが好ましい。 The polymer cement composition of the present invention contains alumina cement, an emulsion and a hardening accelerator, and preferably further contains a filler.
本発明のポリマーセメント組成物において、
エマルジョンの固形分100質量部に対し、アルミナセメントを好ましくは3〜175質量部、さらに好ましくは5〜100質量部、より好ましくは10〜85質量部、特に好ましくは20〜60質量部含むことにより、
(1)水和反応により組成物の乾燥を促進させ、硬化した塗膜の耐水性及び強度確保に優れ、
(2)エマルジョンの固形分100質量部に対し、アルミナセメントの含有量が、上記範囲より小さい場合は塗膜の乾燥時間、強度が不十分となり、また上記範囲より大きい場合ポットライフが短く、また粘度が上昇して作業性、施工性に支障を来す場合があり好ましくない。
本発明のポリマーセメント組成物では、塗膜の乾燥時間が、1〜4.75時間、好ましくは1.5〜4.5、さらに好ましくは2〜4.5時間とすることができ、施工性に優れる。
In the polymer cement composition of the present invention,
By containing alumina cement preferably 3 to 175 parts by mass, more preferably 5 to 100 parts by mass, more preferably 10 to 85 parts by mass, and particularly preferably 20 to 60 parts by mass with respect to 100 parts by mass of the solid content of the emulsion. ,
(1) Promoting the drying of the composition by a hydration reaction, excellent in ensuring water resistance and strength of the cured coating film,
(2) When the content of alumina cement is less than the above range with respect to 100 parts by mass of the solid content of the emulsion, the drying time and strength of the coating film are insufficient, and when it is greater than the above range, the pot life is short, It is not preferable because the viscosity increases and the workability and workability may be hindered.
In the polymer cement composition of the present invention, the drying time of the coating film can be 1 to 4.75 hours, preferably 1.5 to 4.5, and more preferably 2 to 4.5 hours. Excellent.
ポリマーセメント組成物は、アルミナセメント100質量部に対し、硬化促進剤を好ましくは0.1〜7質量部、さらに好ましくは0.5〜6質量部、より好ましくは0.8〜5質量部、特に好ましくは3〜5質量部含むことが、コンクリート層上のポリマーセメント組成物の硬化物層のふくれの発生を抑制するために好ましい。 The polymer cement composition is preferably 0.1 to 7 parts by weight, more preferably 0.5 to 6 parts by weight, more preferably 0.8 to 5 parts by weight, based on 100 parts by weight of the alumina cement. The content of 3 to 5 parts by mass is particularly preferable in order to suppress the occurrence of blistering of the cured layer of the polymer cement composition on the concrete layer.
ポリマーセメント組成物は、エマルジョンの固形分100質量部に対し、アルミナセメントを好ましくは3〜175質量部、さらに好ましくは5〜100質量部、より好ましくは10〜85質量部、特に好ましくは20〜60質量部含み、アルミナセメント100質量部に対し、炭酸リチウムを好ましくは0.1〜7質量部、さらに好ましくは0.5〜6質量部、より好ましくは2質量部を超えて5質量部以下、特に好ましくは3〜5質量部含むことが、ポリマーセメント組成物の粘度を上げずに施工性を確保し、さらにコンクリート層上のポリマーセメント組成物の硬化物層のふくれの発生を抑制するために好ましい。 The polymer cement composition is preferably 3 to 175 parts by mass of alumina cement, more preferably 5 to 100 parts by mass, more preferably 10 to 85 parts by mass, and particularly preferably 20 to 100 parts by mass with respect to 100 parts by mass of the solid content of the emulsion. 60 parts by mass, and 0.1 to 7 parts by mass, more preferably 0.5 to 6 parts by mass, more preferably more than 2 parts by mass and 5 parts by mass or less with respect to 100 parts by mass of alumina cement. In particular, 3 to 5 parts by mass is preferably included to ensure workability without increasing the viscosity of the polymer cement composition and to suppress the occurrence of swelling of the cured layer of the polymer cement composition on the concrete layer. Is preferable.
本発明のポリマーセメント組成物において、エマルジョンの固形分100質量部に対し、アルミナセメント及び充填材とを好ましくは20〜350質量部、さらに好ましくは30〜300質量部、より好ましくは50〜250質量部、特に好ましくは100〜230質量部を含むことが好ましい。
アルミナセメントと充填材とを含む粉体が、エマルジョンの固形分に対して含まれる割合が、上記範囲より大きい場合、得られるポリマーセメント組成物の粘度が高くなり施工性が低下するとともに、十分な下地ひび割れ追従性が得られないため好ましくなく、上記範囲より小さい場合、十分な下地ひび割れ追従性が得られるが、塗膜強度が低下すること、塗膜のタックが強くなるなど好ましくない。
In the polymer cement composition of the present invention, the alumina cement and the filler are preferably 20 to 350 parts by weight, more preferably 30 to 300 parts by weight, and more preferably 50 to 250 parts by weight with respect to 100 parts by weight of the solid content of the emulsion. Part, particularly preferably 100 to 230 parts by weight.
When the ratio of the powder containing the alumina cement and the filler to the solid content of the emulsion is larger than the above range, the resulting polymer cement composition has a high viscosity and the workability is lowered. Substrate crack followability is not obtained, and this is not preferable. If it is smaller than the above range, sufficient base crack followability can be obtained, but this is not preferable because the coating film strength is lowered and the tackiness of the coating film is increased.
本発明においてエマルジョンとは、合成樹脂エマルジョンであり、ポリ酢酸ビニルエマルジョン、エチレンと酢酸ビニルを共重合して得られるエチレン−酢酸ビニル系エマルジョン; エチレン、酢酸ビニルと(メタ)クリル酸誘導体の共重合体エマルジョン、エチレンと(メタ)クリル酸誘導体との共重合体エマルジョン、ポリ(メタ)クリル酸誘導体のエマルジョン、スチレンと(メタ)クリル酸誘導体との共重合体エマルジョンなどの(メタ)クリル酸誘導体を含むアクリル系樹脂エマルジョン、ポリクロロプレンラテックス、酢酸ビニルと塩化ビニルの共重合体エマルジョン、スチレンとブタジエンの共重合体エマルジョン、アクリロニトリとブタジエンの共重合体エマルジョンなどを少なくとも1種含む合成樹脂のエマルジョンを用いることができる。(メタ)クリル酸誘導体は、アクリル酸及びメタクリル酸、これらのエステルなどの酸誘導体を意味する。
エマルジョンとしては、エチレン−酢酸ビニル系エマルジョン、アクリル系樹脂エマルジョンなどの建築用途に開発された樹脂系エマルジョン、さらにエチレン−酢酸ビニル系エマルジョン、アクリル系樹脂エマルジョンなどの建築用途に開発されたポリマー成分のガラス転移温度が0℃以下の樹脂系エマルジョンを好ましく用いることができる。
エマルジョンに含まれるポリマー成分のガラス転移温度は、どのようなものでも用いることができるが、好ましくは0℃以下のもの、さらに好ましくは−45〜0℃、より好ましくは−45〜−5℃ものであれば特に制限はなく用いることが出来る。
エマルジョンは、ポリマー成分のガラス転移温度が0℃以下のものを含むエマルジョン、さらに好ましくはポリマー成分のガラス転移温度が0℃以下のものを50重量%以上含むエマルジョン、特に好ましくはポリマー成分のガラス転移温度が0℃以下のものを80重量%以上含むエマルジョンを用いることが好ましい。
エマルジョンは、ガラス転移温度が0℃以下のエチレン−酢酸ビニル系エマルジョン及びガラス転移温度が0℃以下のアクリル系エマルジョンから選択されるエマルジョンを含むことが好ましい。
エマルジョンの固形分は、水などの溶媒を除去した後のポリマー成分を主成分とする固形物の質量である。
In the present invention, the emulsion is a synthetic resin emulsion, a polyvinyl acetate emulsion, an ethylene-vinyl acetate emulsion obtained by copolymerizing ethylene and vinyl acetate; a copolymer of ethylene, vinyl acetate and a (meth) acrylic acid derivative. (Meth) acrylic acid derivatives such as coalescence emulsion, copolymer emulsion of ethylene and (meth) acrylic acid derivative, emulsion of poly (meth) acrylic acid derivative, copolymer emulsion of styrene and (meth) acrylic acid derivative A synthetic resin emulsion containing at least one kind of acrylic resin emulsion containing polychloroprene latex, copolymer emulsion of vinyl acetate and vinyl chloride, copolymer emulsion of styrene and butadiene, copolymer emulsion of acrylonitrile and butadiene, etc. for Can be. The (meth) acrylic acid derivative means acid derivatives such as acrylic acid, methacrylic acid, and esters thereof.
Emulsions include resin-based emulsions developed for architectural applications such as ethylene-vinyl acetate emulsions and acrylic resin emulsions, and polymer components developed for architectural applications such as ethylene-vinyl acetate emulsions and acrylic resin emulsions. A resin emulsion having a glass transition temperature of 0 ° C. or lower can be preferably used.
Any glass transition temperature can be used for the polymer component contained in the emulsion, but it is preferably 0 ° C. or lower, more preferably −45 to 0 ° C., and more preferably −45 to −5 ° C. If there is no particular limitation, it can be used.
The emulsion contains an emulsion having a glass transition temperature of the polymer component of 0 ° C. or less, more preferably an emulsion containing 50% by weight or more of the polymer component having a glass transition temperature of 0 ° C. or less, particularly preferably a glass transition of the polymer component. It is preferable to use an emulsion containing 80% by weight or more of one having a temperature of 0 ° C. or lower.
The emulsion preferably includes an emulsion selected from an ethylene-vinyl acetate emulsion having a glass transition temperature of 0 ° C. or lower and an acrylic emulsion having a glass transition temperature of 0 ° C. or lower.
The solid content of the emulsion is the mass of a solid material mainly composed of a polymer component after removing a solvent such as water.
エマルジョンにおいて、エチレン−酢酸ビニル系エマルジョン又はガラス転移温度が0℃以下のエチレン−酢酸ビニル系エマルジョンを用いる場合には、好ましくはエチレン−酢酸ビニル系エマルジョンを50質量%以上含むエマルジョン、さらに好ましくはエチレン−酢酸ビニル系エマルジョンを60質量%以上含むエマルジョン、特に好ましくはエチレン−酢酸ビニル系エマルジョンを70質量%以上含むエマルジョンを用いることが好ましい。
エマルジョンにおいて、アクリル系樹脂エマルジョン又はガラス転移温度が0℃以下のアクリル系樹脂エマルジョンを用いる場合には、好ましくはアクリル系樹脂エマルジョンを5質量%以上含むエマルジョン、さらに好ましくはアクリル系樹脂エマルジョンを10質量%以上含むエマルジョン、特に好ましくはアクリル系樹脂エマルジョンを20質量%以上含むエマルジョンを用いることが好ましい。
エマルジョンにおいて、特にエチレン−酢酸ビニル系エマルジョン及びアクリル系樹脂エマルジョンを含むエマルジョンを、又は、ガラス転移温度が0℃以下のエチレン−酢酸ビニル系エマルジョン及びガラス転移温度が0℃以下のアクリル系樹脂エマルジョンを含むエマルジョンを用いる場合には、エチレン−酢酸ビニル系エマルジョンを50質量%以上及びアクリル系樹脂エマルジョンを50質量%以下含むエマルジョン、さらに好ましくはエチレン−酢酸ビニル系エマルジョンを60質量%以上及びアクリル系樹脂エマルジョンを40質量%以下含む含むエマルジョン、特に好ましくはエチレン−酢酸ビニル系エマルジョンを70質量%以上及びアクリル系樹脂エマルジョンを30質量%以下含むエマルジョンを用いることが好ましい。
In the case of using an ethylene-vinyl acetate emulsion or an ethylene-vinyl acetate emulsion having a glass transition temperature of 0 ° C. or lower in the emulsion, the emulsion preferably contains 50% by mass or more of an ethylene-vinyl acetate emulsion, more preferably ethylene. -It is preferable to use an emulsion containing 60% by mass or more of a vinyl acetate emulsion, particularly preferably an emulsion containing 70% by mass or more of an ethylene-vinyl acetate emulsion.
When an acrylic resin emulsion or an acrylic resin emulsion having a glass transition temperature of 0 ° C. or lower is used in the emulsion, the emulsion preferably contains 5% by mass or more of the acrylic resin emulsion, more preferably 10% by mass of the acrylic resin emulsion. %, Particularly preferably an emulsion containing 20% by mass or more of an acrylic resin emulsion.
In particular, an emulsion including an ethylene-vinyl acetate emulsion and an acrylic resin emulsion, or an ethylene-vinyl acetate emulsion having a glass transition temperature of 0 ° C. or less and an acrylic resin emulsion having a glass transition temperature of 0 ° C. or less. In the case of using an emulsion containing 50 wt% or more of an ethylene-vinyl acetate emulsion and 50 wt% or less of an acrylic resin emulsion, more preferably 60 wt% or more of an ethylene-vinyl acetate emulsion and an acrylic resin. It is preferable to use an emulsion containing 40% by mass or less of an emulsion, particularly preferably an emulsion containing 70% by mass or more of an ethylene-vinyl acetate emulsion and 30% by mass or less of an acrylic resin emulsion.
エマルジョンは、公知の製造方法により得られるものを用いることができ、例えば、乳化剤の存在下に、重合開始剤を用いて、水又は含水溶媒中で合成樹脂の原料となる重合性モノマーを乳化重合する方法などにより製造することができる。 As the emulsion, one obtained by a known production method can be used. For example, by using a polymerization initiator in the presence of an emulsifier, a polymerizable monomer that is a raw material for a synthetic resin is emulsion-polymerized in water or a hydrous solvent. It can manufacture by the method to do.
乳化剤としては、公知のものを用いることができ、アニオン性、ノニオン性、カチオン性又は両性の界面活性剤やポリビニルアルコール等の保護コロイドなどを挙げることができる。
重合開始剤としては、水又は含水溶媒中でラジカル重合できるものが好ましく、過酸化水素、過酢酸、過硫酸又はこれらのアンモニウム塩や硫酸塩等の水溶性の過酸化物やその塩などを挙げることができる。また、ベンゾイルパーオキサイド、t−ブチルハイドロパーオキサイド、2,2’−アゾビスイソブチルニトリルなどの有機過酸化物、メタ亜硫酸ナトリウムやピロ亜硫酸ナトリウムなどの還元剤を併用することができる。
重合開始剤の使用量は、エマルジョンが製造できる範囲であれば適宜選択できる。
As the emulsifier, known ones can be used, and examples thereof include anionic, nonionic, cationic or amphoteric surfactants and protective colloids such as polyvinyl alcohol.
As the polymerization initiator, those capable of radical polymerization in water or a hydrous solvent are preferable, and examples thereof include hydrogen peroxide, peracetic acid, persulfuric acid, water-soluble peroxides such as ammonium salts and sulfates thereof, and salts thereof. be able to. Further, organic peroxides such as benzoyl peroxide, t-butyl hydroperoxide, 2,2′-azobisisobutylnitrile, and reducing agents such as sodium metasulfite and sodium pyrosulfite can be used in combination.
The amount of the polymerization initiator used can be appropriately selected as long as the emulsion can be produced.
エマルジョンは、水又は含水溶媒を含まない粉末状の合成樹脂粒子を含み、粉末状の合成樹脂粒子を用いると、水又は含水溶媒を除いた全成分を一つのパッケージとすることができ、施工現場では水を添加するだけで使用できるので便利である。 The emulsion contains powdery synthetic resin particles that do not contain water or a water-containing solvent. When powdery synthetic resin particles are used, all components excluding water or the water-containing solvent can be made into one package, and the construction site Then, it can be used simply by adding water.
水又は含水溶媒を含まない粉末状の合成樹脂を除く水又は含水溶媒を含むエマルジョンでは、エマルジョン中に含まれるポリマーの固形分は適宜選択することができるが、エマルジョン中に含まれるポリマーの固形分はエマルジョン100質量部中、30〜80質量部が好ましく、40〜60質量部がより好ましい。30質量部未満だと硬化しにくいおそれがあり、80質量部を越えると粘度が大きすぎて作業性が低下したり、塗膜を均一に形成できない場合が考えられる。 In an emulsion containing water or a water-containing solvent excluding powdered synthetic resin not containing water or a water-containing solvent, the solid content of the polymer contained in the emulsion can be appropriately selected. Is preferably 30 to 80 parts by mass, more preferably 40 to 60 parts by mass in 100 parts by mass of the emulsion. If it is less than 30 parts by mass, it may be difficult to cure. If it exceeds 80 parts by mass, the viscosity may be too high and workability may be reduced, or a coating film may not be formed uniformly.
エチレン−酢酸ビニル共重合体エマルジョンは、エチレンと酢酸ビニルとを共重合した公知のエマルジョンを用いることが出来る。
エチレン酢酸ビニル共重合体エマルジョンとしては、ポリビニルアルコール、セルロース誘導体などの水溶性高分子を乳化剤や保護コロイドとして用いる物を好ましく用いることが出来る。特にエチレン酢酸ビニル共重合体エマルジョンは、保護コロイドとしてポリビニルアルコールを用いたものが好ましい。
エチレン−酢酸ビニル共重合体エマルジョンの重合体成分において、酢酸ビニル含有量は、好ましくは30〜90質量%、さらに好ましくは50〜90質量%、特に好ましくは60〜86質量%が好ましい。
エチレン酢酸ビニル共重合体エマルジョン中のエチレン酢酸ビニル共重合体成分の含有量は、好ましくは40〜65質量%、さらに好ましくは45〜60質量%、特に好ましくは47〜60質量%である。
As the ethylene-vinyl acetate copolymer emulsion, a known emulsion obtained by copolymerizing ethylene and vinyl acetate can be used.
As the ethylene vinyl acetate copolymer emulsion, a product using a water-soluble polymer such as polyvinyl alcohol or cellulose derivative as an emulsifier or protective colloid can be preferably used. In particular, the ethylene vinyl acetate copolymer emulsion is preferably one using polyvinyl alcohol as a protective colloid.
In the polymer component of the ethylene-vinyl acetate copolymer emulsion, the vinyl acetate content is preferably 30 to 90% by mass, more preferably 50 to 90% by mass, and particularly preferably 60 to 86% by mass.
The content of the ethylene vinyl acetate copolymer component in the ethylene vinyl acetate copolymer emulsion is preferably 40 to 65% by mass, more preferably 45 to 60% by mass, and particularly preferably 47 to 60% by mass.
アクリル系樹脂エマルジョンとしては、メチル(メタ)アクリレート、エチル(メタ)アクリレート、ブチル(メタ)アクリレート、2−エチルヘキシル(メタ)アクリレートなどのアルキル(メタ)アクリレートなど(メタ)アクリレート化合物などを1種または2種以上を重合したもの、さらにこれらのモノマーと共重合可能なスチレン、酢酸ビニル、塩化ビニリデンなどのビニル化合物と共重合させたものを用いることが出来る。(メタ)アクリレートとは、メタクリレート及びアクリレートを意味する。
アクリル系樹脂エマルジョンは、エマルジョンに含まれるポリマー成分が、架橋していないポリマー、さらに好ましくはポリマー内又はポリマー間で架橋していないポリマーを用いることにより、伸びに優れるために好ましい。
アクリル系樹脂エマルジョンは、公知の乳化剤や保護コロイドを用いることができ、例えば、ポリビニルアルコール、セルロース誘導体などの水溶性高分子、非イオン界面活性剤、イオン性界面活性剤などの乳化剤や保護コロイドを用いることが出来る。
アクリル系樹脂エマルジョンは、公知のエマルジョンを用いることができ、アクリル系樹脂成分の含有量は特に制限がない。
As the acrylic resin emulsion, one or more (meth) acrylate compounds such as alkyl (meth) acrylate such as methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, or the like Those obtained by polymerizing two or more kinds, and those obtained by copolymerization with vinyl compounds such as styrene, vinyl acetate and vinylidene chloride which can be copolymerized with these monomers can be used. (Meth) acrylate means methacrylate and acrylate.
The acrylic resin emulsion is preferable because the polymer component contained in the emulsion is excellent in elongation by using a polymer that is not crosslinked, more preferably a polymer that is not crosslinked within or between polymers.
For the acrylic resin emulsion, known emulsifiers and protective colloids can be used. For example, water-soluble polymers such as polyvinyl alcohol and cellulose derivatives, emulsifiers and protective colloids such as nonionic surfactants and ionic surfactants can be used. Can be used.
As the acrylic resin emulsion, a known emulsion can be used, and the content of the acrylic resin component is not particularly limited.
本発明のポリマーセメント組成物は、エマルジョンの他に、ワックスサスペンションを含むことが出来る。
ワックスサスペンションとしては、パラフィンワックスサスペンション、オレフィンワックスサスペンション、フィッシャートロプシュワックスサスペンションなどの水分散型などの公知のワックスサスペンションを用いることが出来る。
パラフィンワックスサスペンションとしては、n−パラフィンを主成分とするパラフィンワックスのサスペンションを用いることが出来る。
オレフィンワックスサスペンションとしては、ポリエチレンワックス、ポリプロピレンワックスなどの低中分子量のポリオレフィンのサスペンションを用いることが出来る。
The polymer cement composition of the present invention can contain a wax suspension in addition to the emulsion.
As the wax suspension, a known wax suspension such as a water dispersion type such as a paraffin wax suspension, an olefin wax suspension, and a Fischer-Tropsch wax suspension can be used.
As the paraffin wax suspension, a suspension of paraffin wax mainly composed of n-paraffin can be used.
As the olefin wax suspension, a suspension of low and medium molecular weight polyolefin such as polyethylene wax and polypropylene wax can be used.
アルミナセメントは、潜在的に急硬性を有しており、硬化後は耐化学薬品性、耐火性に優れた硬化体を与える。アルミナセメントは鉱物組成が異なるものが数種知られ市販されており、何れも主成分はモノカルシウムアルミネート(CA)であるが、強度および着色性の面からは、CA成分が多く且つC4AF等の少量成分が少ないアルミナセメントが好ましい。
本発明のポリマーセメント組成物において、セメント成分としてはアルミナセメント単独で用いることが好ましく、アルミナセメントのほかに本発明の特性を損なわない範囲でポルトランドセメント、石膏、高炉スラグなどの水硬性成分を含んでもよい。
Alumina cement has a potentially rapid hardening property, and gives a cured product excellent in chemical resistance and fire resistance after curing. Alumina cement is commercially available is known several those mineral composition is different, but both major component is monocalcium aluminate (CA), from the viewpoint of strength and coloring, CA component number and C 4 Alumina cement with a small amount of small components such as AF is preferred.
In the polymer cement composition of the present invention, it is preferable to use alumina cement alone as the cement component. In addition to alumina cement, it contains hydraulic components such as Portland cement, gypsum and blast furnace slag as long as the characteristics of the present invention are not impaired. But you can.
充填材は、珪砂、スラグ粉、フライアッシュ、石灰石粉、タルク、カオリン、アルミナ粉、酸化チタン、水酸化アルミニウム、マイカ、パイロフィライトなどを添加して用いることが出来、これらの充填材を1種または2種以上用いることが出来る。特に珪砂の場合、表面精度の面から5〜7号の使用が好ましい。
本発明のポリマーセメント組成物は、充填材としてタルクを含むことが好ましく、さらにタルク及び珪砂を含むことが好ましい。
本発明のポリマーセメント組成物は、エマルジョンの固形分100質量部に対し、充填材としてタルクを好ましくは0.1〜40質量部、さらに好ましくは1〜35質量部、より好ましくは5〜30質量部、特に好ましくは15〜25質量部を含むことが好ましく、さらにタルク0.1〜40質量部及び珪砂17〜300質量部含むことが好ましい。
The filler can be used by adding silica sand, slag powder, fly ash, limestone powder, talc, kaolin, alumina powder, titanium oxide, aluminum hydroxide, mica, pyrophyllite, etc. Two or more species can be used. In particular, in the case of silica sand, use of No. 5 to 7 is preferable in terms of surface accuracy.
The polymer cement composition of the present invention preferably contains talc as a filler, and further preferably contains talc and silica sand.
The polymer cement composition of the present invention is preferably 0.1 to 40 parts by weight, more preferably 1 to 35 parts by weight, more preferably 5 to 30 parts by weight of talc as a filler with respect to 100 parts by weight of the solid content of the emulsion. Parts, particularly preferably 15 to 25 parts by mass, and further preferably 0.1 to 40 parts by mass of talc and 17 to 300 parts by mass of silica sand.
硬化促進剤としては、公知のリチウム塩で、炭酸リチウム、塩化リチウム、硫酸リチウム、硝酸リチウム、水酸化リチウム、酢酸リチウム、酒石酸リチウム、リンゴ酸リチウム、クエン酸リチウムなどの有機系及び無機系のリチウム塩を用いることができる。硬化促進剤としては、特に炭酸リチウムを含む又は炭酸リチウムを用いることが、ふくれの抑制効果、入手容易性、価格の面から好ましい。
リチウム塩は、リチウム塩の粒径は50μm以下、さらに30μm以下、特に10μm以下が、溶解性に優れ、微細な多数の斑点となり表面の美観を損なうことがないために好ましい。
Curing accelerators are known lithium salts such as lithium carbonate, lithium chloride, lithium sulfate, lithium nitrate, lithium hydroxide, lithium acetate, lithium tartrate, lithium malate, lithium citrate, and other organic and inorganic lithium. A salt can be used. As the curing accelerator, it is particularly preferable to contain lithium carbonate or use lithium carbonate from the viewpoint of the suppression effect of blistering, availability, and cost.
The lithium salt preferably has a lithium salt particle size of 50 μm or less, more preferably 30 μm or less, and particularly preferably 10 μm or less because it has excellent solubility and does not impair the appearance of the surface due to many fine spots.
本発明のポリマーセメント組成物は、硬化時間や流動性を調整するため、又は本発明の特性を損なわない範囲で添加剤を含むことが出来る。
添加剤としては、本発明の用いる硬化促進剤を除く一般的に用いられる凝結遅延剤や凝結促進剤などの凝結速度調整剤、減水剤、流動化剤、消泡剤、増粘剤などを挙げることが出来る。
The polymer cement composition of the present invention can contain additives in order to adjust the setting time and fluidity, or within a range not impairing the characteristics of the present invention.
Examples of the additive include commonly used setting retarders such as setting retarders and setting accelerators other than the curing accelerator used in the present invention, water reducing agents, fluidizers, antifoaming agents, thickeners, and the like. I can do it.
本発明の防水用ポリマーセメント組成物は、塗膜の強度を向上させる目的で、ガラス繊維を含むことができる。 The waterproof polymer cement composition of the present invention can contain glass fibers for the purpose of improving the strength of the coating film.
本発明の防水用ポリマーセメント組成物は、塗膜の強度や防水性を向上させる目的で、消泡剤を含むことが好ましい。
消泡剤は、シリコン系、アルコール系、ポリエーテル、フッ素系などの合成物質または植物由来の天然物質など、公知のものを用いることが出来る。
消泡剤の添加量は、本発明の特性を損なわない範囲で添加することができ、アルミナセメント及びエマルジョンの固形分と、必要に応じて添加されるタルクや珪砂などの固形分との合計量100質量部に対して、2質量部以下、特に0.2質量部以下が好ましい。消泡剤の添加量は、上記より多く添加する場合、消泡効果の向上がみとめられない場合がある。
The waterproof polymer cement composition of the present invention preferably contains an antifoaming agent for the purpose of improving the strength and waterproofness of the coating film.
As the antifoaming agent, known materials such as synthetic materials such as silicon-based, alcohol-based, polyether, and fluorine-based materials or plant-derived natural materials can be used.
The defoaming agent can be added within a range that does not impair the properties of the present invention. The total amount of solids of alumina cement and emulsion and solids such as talc and silica sand added as necessary. 2 parts by mass or less, particularly 0.2 parts by mass or less is preferable with respect to 100 parts by mass. When the defoaming agent is added in a larger amount than the above, the defoaming effect may not be improved.
本発明のポリマーセメント組成物は、
(1)コンクリート層に、ポリマーセメント組成物の硬化物層を積層することによりコンクリート構造体を得ることが出来る。また、コンクリート層に、ポリマーセメント組成物の硬化物層を直接又は積層することができる。
本発明のポリマーセメント組成物は、コンクリート層にプライマーの硬化物層を設け、さらにポリマーセメント組成物の硬化物層の順に積層することによりコンクリート構造体を得ることが出来る。また、コンクリート層にプライマーの硬化物層を直接設けることができ、さらにプライマーの硬化物層に、ポリマーセメント組成物の硬化物層を直接積層することができる。
The polymer cement composition of the present invention comprises:
(1) A concrete structure can be obtained by laminating a cured layer of a polymer cement composition on a concrete layer. Moreover, the hardened | cured material layer of a polymer cement composition can be directly or laminated | stacked on a concrete layer.
In the polymer cement composition of the present invention, a concrete structure can be obtained by providing a hardened material layer of a primer on a concrete layer and further laminating the hardened material layer of the polymer cement composition in this order. Moreover, the hardened | cured material layer of a primer can be directly provided in a concrete layer, and also the hardened | cured material layer of a polymer cement composition can be directly laminated | stacked on the hardened | cured material layer of a primer.
本発明のコンクリート構造体の施工の一例を示すと、
(1)コンクリート又はモルタルを屋上、床面又は壁に打設し、コテ、機械等で仕上げた後、コンクリート又はモルタルを硬化させてコンクリート層を形成させ、(2)プライマーの硬化物層表面に、本発明のポリマーセメント組成物をローラー、コテ及びスプレーなどを用いる一般的方法で塗布し、その後ポリマーセメント組成物を硬化させた硬化物層を形成させることにより、コンクリート構造体を施工することができる。
When showing an example of the construction of the concrete structure of the present invention,
(1) After placing concrete or mortar on the roof, floor or wall and finishing it with a trowel, machine, etc., the concrete or mortar is cured to form a concrete layer. (2) On the cured product layer surface of the primer The concrete structure can be applied by applying the polymer cement composition of the present invention by a general method using a roller, a trowel, a spray, and the like, and then forming a cured product layer obtained by curing the polymer cement composition. it can.
本発明のコンクリート構造体のプライマーの硬化物層を有する施工の一例を示すと、
(1)コンクリート又はモルタルを屋上、床面又は壁に打設し、コテ、機械等で仕上げた後、コンクリート又はモルタルを硬化させてコンクリート層を形成させ、(2)コンクリート層表面に、プライマー(エマルジョンの希釈液又は希釈水溶液)をローラー、コテ及びスプレーなどを用いる一般的方法で塗布又は吹き付けを行い、その後プライマーを硬化させた硬化物層を形成させ、
(3)プライマーの硬化物層表面に、本発明のポリマーセメント組成物をローラー、コテ及びスプレーなどを用いる一般的方法で塗布し、その後ポリマーセメント組成物を硬化させた硬化物層を形成させることにより、コンクリート構造体を施工することができる。
When showing an example of construction having a cured product layer of the primer of the concrete structure of the present invention,
(1) After placing concrete or mortar on the roof, floor or wall and finishing it with a trowel, machine, etc., the concrete or mortar is cured to form a concrete layer. (2) Primer ( Emulsion diluted solution or diluted aqueous solution) is applied or sprayed by a general method using a roller, a trowel and a spray, and then a cured product layer is formed by curing the primer,
(3) Applying the polymer cement composition of the present invention to the surface of the cured product layer of the primer by a general method using a roller, a trowel and a spray, and then forming a cured product layer obtained by curing the polymer cement composition. Thus, a concrete structure can be constructed.
プライマーの硬化物層は、プライマーとして公知のエチレン−酢酸ビニル共重合体系エマルジョン、アクリル系樹脂エマルジョンなどのエマルジョンを用いることができ、これらのエマルジョンの硬化物からなる層が好ましい。
プライマーの硬化物層は、本発明のポリマーセメント組成物に含まれるエマルジョンと同じ樹脂成分を用いること又は本発明のポリマーセメント組成物に使用するエマルジョンと同じ樹脂成分を用いることが、プライマー層と本発明のポリマーセメント組成物との層間の接着強度が優れるために好ましい。
As the primer cured product layer, known primers such as ethylene-vinyl acetate copolymer emulsions and acrylic resin emulsions can be used, and a layer made of a cured product of these emulsions is preferred.
The cured product layer of the primer uses the same resin component as the emulsion contained in the polymer cement composition of the present invention or uses the same resin component as the emulsion used in the polymer cement composition of the present invention. It is preferable because the adhesive strength between the layers with the polymer cement composition of the invention is excellent.
本発明のポリマーセメント組成物は、コンクリート防水用、コンクリート床防水用、コンクリート屋上防水用などの防水用途に用いることが出来、コンクリートの被施工物表面に塗布したコンクリート構造体を得ることが出来る。 The polymer cement composition of the present invention can be used for waterproofing applications such as concrete waterproofing, concrete floor waterproofing, concrete rooftop waterproofing, and the like, and a concrete structure coated on the surface of concrete work can be obtained.
本発明のポリマーセメント組成物は、攪拌容器にエマルジョンを所定量計量し、攪拌機でエマルジョンを攪拌しながら所定量のアルミナセメント、炭酸リチウムなどの硬化促進剤、さらに必要に応じて充填材や添加剤などを添加し、数分間攪拌・混合して調整することができる。その際水の添加は、材料分離及び塗膜物性低下の面から行わないほうが好ましい。
アルミナセメント、炭酸リチウムなどの硬化促進剤、充填材或いは添加剤などは、単独で添加しても良いし、予め他の数種と混合したものを添加しても良く、添加順序は特に選ばない。また、攪拌機は、一般的な固液攪拌機など撹拌機能を有するものを問題なく用いることが出来る。
The polymer cement composition of the present invention measures a predetermined amount of an emulsion in a stirring vessel, and while stirring the emulsion with a stirrer, a predetermined amount of a hardening accelerator such as alumina cement or lithium carbonate, and further, if necessary, a filler or an additive Etc., and can be adjusted by stirring and mixing for several minutes. In that case, it is preferable not to add water from the viewpoint of material separation and film property deterioration.
A hardening accelerator such as alumina cement and lithium carbonate, a filler or an additive may be added alone, or may be added in advance mixed with other several kinds, and the order of addition is not particularly limited. . Moreover, what has a stirring function, such as a general solid-liquid stirrer, can be used for a stirrer without a problem.
本発明のポリマーセメント組成物及びプライマーは、刷毛、ローラー、コテ及びスプレーなどを用いる一般的方法で被施工物表面に塗布などの方法で施工される。ポリマーセメント組成物の施工された層は、乾燥、硬化後に更に同じ操作を繰り返し、複数の硬化層を形成させるのが好ましい。また、屋上などの施工でメッシュを硬化物間に挟んだ構造とする場合には、乾燥後のポリマーセメント組成物上にメッシュを置き、メッシュの上からポリマーセメント組成物を施工してメッシュを固定する工程を加える工法が採用できる。さらに、最外層に別の組成物や材料を施工・乾燥させた保護層を形成させて仕上げることも可能である。 The polymer cement composition and the primer of the present invention are applied by a method such as application to the surface of an object by a general method using a brush, a roller, a trowel and a spray. It is preferable that the applied layer of the polymer cement composition repeats the same operation after drying and curing to form a plurality of cured layers. In addition, when constructing a structure in which the mesh is sandwiched between hardened materials by construction on the rooftop, place the mesh on the polymer cement composition after drying, and fix the mesh by constructing the polymer cement composition from above the mesh It is possible to adopt a method of adding a process to perform. Furthermore, it is also possible to finish by forming a protective layer in which another composition or material is applied and dried on the outermost layer.
本発明のポリマーセメント組成物において、20℃の可使時間は、好ましくは0.25時間以上、さらに好ましくは0.35時間以上、特に好ましくは0.5時間以上が、作業時間確保のために好ましい。 In the polymer cement composition of the present invention, the pot life of 20 ° C. is preferably 0.25 hours or more, more preferably 0.35 hours or more, and particularly preferably 0.5 hours or more in order to ensure working time. preferable.
本発明のポリマーセメント組成物は、スラリー粘度が、好ましくは5〜100Pa・s、さらに好ましくは10〜75Pa・s、特に好ましくは10〜50Pa・sが、ダレ防止及びコテ作業性確保のために好ましい。 The polymer cement composition of the present invention has a slurry viscosity of preferably 5 to 100 Pa · s, more preferably 10 to 75 Pa · s, and particularly preferably 10 to 50 Pa · s, in order to prevent sagging and to ensure the workability of the iron. preferable.
以下、本発明を実施例に基づき、さらに詳細に説明する。但し、本発明は下記実施例により制限されるものでない。 Hereinafter, the present invention will be described in more detail based on examples. However, the present invention is not limited by the following examples.
塗膜物性の評価は以下のように行う。
(1)スラリー粘度測定法: 20℃室温にて、表1に示す各成分及びその配合割合で容器中に所定量を計量し、攪拌後ポリマーセメント組成物を調製し、直ちに(株)トキメック製DVH−BII型粘度計により、ローターNo.6を用い回転数20rpmの条件で粘度を測定する。
(2)20℃の可使時間の評価法:20℃室温にて、表1に示すポリマーセメント組成物を調製後、スレート板(各実施例及び比較例と同じエマルジョンを用い、エマルジョンに水を添加し10倍に希釈した液(プライマー)を、スレート表面に0.4kg/m2の量で塗布し1日放置する)にコテ塗りしたさい、ポリマーセメント組成物がコテで良く延びなくなった状態までの経過時間を測定する。
(3)60℃のふくれ発生量の評価法:20℃室温にて、表1に示すポリマーセメント組成物を調製後、300×300×4mmのスレート板(各実施例及び比較例と同じエマルジョンを用い、エマルジョンに水を添加し10倍に希釈した液(プライマー)を、スレート表面に0.4kg/m2の量で塗布し1日放置し、評価前1時間60℃の乾燥器中に放置する)に0.9kg/m2コテ塗りし、直ちに60℃の乾燥器に入れ、10分後、20分後、30分後に塗膜表面のふくれ発生量を目視で観察する。
Evaluation of physical properties of the coating film is performed as follows.
(1) Slurry viscosity measurement method: At 20 ° C., room temperature, each component shown in Table 1 and its blending ratio are weighed into a container, and after stirring, a polymer cement composition is prepared. Immediately manufactured by Tokimec Co., Ltd. With a DVH-BII viscometer, the rotor No. 6 is used to measure the viscosity under the condition of a rotation speed of 20 rpm.
(2) Evaluation method of pot life at 20 ° C .: After preparing the polymer cement composition shown in Table 1 at 20 ° C., use a slate plate (the same emulsion as in each example and comparative example, When the solution (primer) added and diluted 10 times is applied to the surface of the slate in an amount of 0.4 kg / m 2 and left for 1 day, the polymer cement composition does not extend well with the iron. Measure the elapsed time until.
(3) Evaluation method of the amount of blistering at 60 ° C .: After preparing the polymer cement composition shown in Table 1 at room temperature of 20 ° C., a 300 × 300 × 4 mm slate plate (the same emulsion as each example and comparative example) A solution (primer) diluted 10-fold by adding water to the emulsion was applied to the slate surface in an amount of 0.4 kg / m 2 and allowed to stand for 1 day, then left in a 60 ° C. dryer for 1 hour before evaluation. 0.9 kg / m 2 , and immediately put in a drier at 60 ° C. After 10 minutes, 20 minutes and 30 minutes, the amount of blistering on the coating film surface is visually observed.
(4)ガラス転移温度: ガラス板上にエマルジョンを適量滴下し、60℃で16時間乾燥し、得られた質量が9.5〜10.5mgの範囲に入った乾燥塗膜を、示差走査熱量計(島津製作所社製、DSC−50)を用い、ガラス転移温度を測定する。
DSCの測定条件は、室温から150℃に10分間で昇温し、150℃を10分間保持した後に計算で得られた試料のTgより50℃低い温度まで下げ、再度150℃まで10分間で昇温するさいに、1回目のTgの測定を行う。次に1回目で測定したTgより50℃低い温度まで下げるさいに、2回目のTgの測定を行い、2回目のTgの値をガラス転移温度とする。
(4) Glass transition temperature: An appropriate amount of emulsion was dropped on a glass plate, dried at 60 ° C. for 16 hours, and the resulting dried coating film having a mass in the range of 9.5 to 10.5 mg was subjected to differential scanning calorimetry. The glass transition temperature is measured using a meter (manufactured by Shimadzu Corporation, DSC-50).
The DSC measurement conditions were as follows: room temperature was raised from 150 ° C. over 10 minutes, held at 150 ° C. for 10 minutes, lowered to a temperature 50 ° C. lower than the Tg of the sample obtained by calculation, and again raised to 150 ° C. over 10 minutes When warming, the first Tg is measured. Next, when the temperature is lowered to 50 ° C. lower than the Tg measured in the first time, the second Tg is measured, and the second Tg value is defined as the glass transition temperature.
実施例1〜4及び比較例1
(1)原料は、以下の物を用いる。
・エマルジョンA:エチレン−酢酸ビニル共重合体エマルジョン(電気化学工業社製、商品名:EVA#59、ポリビニルアルコールを保護コロイドとしたもの、エマルジョンA中の固形分成分含有量:56重量%、エマルジョンA中の酢酸ビニル重合体成分含有量:41重量%、ガラス転移温度:−15℃)。
・エマルジョンB:アクリル系重合体エマルジョン(高圧ガス工業社製、商品名:ぺガール842、エマルジョンB中の固形分成分含有量:54重量%、ガラス転移温度:−15℃)。
・アルミナセメント:市販アルミナセメント(JIS・R−2511による第3種)。
・珪砂:市販6号珪砂。
・タルク:日本タルク製、商品名:タルクS。
・炭酸リチウム(市販品)(粒径:10μm以下のものを使用)。
Examples 1 to 4 and Comparative Example 1
(1) The following materials are used as raw materials.
Emulsion A: ethylene-vinyl acetate copolymer emulsion (manufactured by Denki Kagaku Kogyo Co., Ltd., trade name: EVA # 59, using polyvinyl alcohol as a protective colloid, solid content in emulsion A: 56% by weight, emulsion Content of vinyl acetate polymer component in A: 41% by weight, glass transition temperature: −15 ° C.).
Emulsion B: Acrylic polymer emulsion (manufactured by High Pressure Gas Industry Co., Ltd., trade name: Pegar 842, solid content in emulsion B: 54% by weight, glass transition temperature: −15 ° C.).
Alumina cement: Commercially available alumina cement (type 3 according to JIS R-2511).
Silica sand: Commercially available No. 6 silica sand.
-Talc: Made by Nippon Talc, Trade name: Talc S.
-Lithium carbonate (commercially available) (particle size: 10 μm or less used).
(2)ポリマーセメント組成物の調製
2Lのポリ容器にエマルジョン、アルミナセメント、珪砂及び炭酸リチウムを、表1に示す配合割合(合計1250g)で加え、0.15KW攪拌機を使用し1300rpmの条件下で3分間混合し、スラリー状のポリマーセメント組成物を得た。
得られたポリマーセメント組成物は、粘度、可使時間及び塗膜のふくれ発生量の評価を行い、結果を表2に示す。
表1の配合割合は、エマルジョンは固形分の重量を示す。
(2) Preparation of polymer cement composition Emulsion, alumina cement, silica sand, and lithium carbonate were added to a 2 L plastic container at a blending ratio shown in Table 1 (total 1250 g), and a 0.15 KW stirrer was used at 1300 rpm. The mixture was mixed for 3 minutes to obtain a slurry polymer cement composition.
The obtained polymer cement composition was evaluated for viscosity, pot life and amount of blistering of the coating film, and the results are shown in Table 2.
The blending ratios in Table 1 indicate the weight of the solid content of the emulsion.
Claims (9)
エマルジョンの固形分100質量部に対し、アルミナセメントと充填材の合計量20〜350質量部を含むことを特徴とする請求項1〜3のいずれか1項に記載のポリマーセメント組成物。 The polymer cement composition further includes a filler,
The solid content 100 parts by weight of the emulsion, the polymer cement composition according to any one of claims 1 to 3, characterized in that it comprises a total amount from 20 to 350 parts by weight of alumina cement and the filler.
ポリマーセメント組成物が請求項1〜7のいずれか1項に記載のポリマーセメント組成物であることを特徴とするコンクリート構造体。 A concrete structure in which a hardened layer of a polymer cement composition is laminated on a concrete layer,
A concrete structure, wherein the polymer cement composition is the polymer cement composition according to any one of claims 1 to 7 .
ポリマーセメント組成物が請求項1〜7のいずれか1項に記載のポリマーセメント組成物であり、
プライマーがエマルジョンであることを特徴とするコンクリート構造体。 A concrete structure in which a hardened material layer of a primer and a hardened material layer of a polymer cement composition are laminated in this order on a concrete layer,
The polymer cement composition is the polymer cement composition according to any one of claims 1 to 7 ,
A concrete structure characterized in that the primer is an emulsion.
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JPS60260457A (en) * | 1984-06-05 | 1985-12-23 | 積水化学工業株式会社 | Polymer cement composition |
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JPH10273357A (en) * | 1997-01-28 | 1998-10-13 | Ube Ind Ltd | Hydraulic coloring finishing material composition |
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