JP4601967B2 - Primer composition, primer, and primer treatment method using the same - Google Patents
Primer composition, primer, and primer treatment method using the same Download PDFInfo
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- JP4601967B2 JP4601967B2 JP2004008868A JP2004008868A JP4601967B2 JP 4601967 B2 JP4601967 B2 JP 4601967B2 JP 2004008868 A JP2004008868 A JP 2004008868A JP 2004008868 A JP2004008868 A JP 2004008868A JP 4601967 B2 JP4601967 B2 JP 4601967B2
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- 239000000203 mixture Substances 0.000 title claims description 23
- 238000000034 method Methods 0.000 title claims description 10
- 150000003839 salts Chemical class 0.000 claims description 27
- 239000004570 mortar (masonry) Substances 0.000 claims description 18
- 239000007787 solid Substances 0.000 claims description 14
- 239000004568 cement Substances 0.000 claims description 10
- 239000002562 thickening agent Substances 0.000 claims description 10
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 claims description 9
- 230000008439 repair process Effects 0.000 claims description 9
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 claims description 8
- 239000004815 dispersion polymer Substances 0.000 claims description 6
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 claims description 4
- 229910052808 lithium carbonate Inorganic materials 0.000 claims description 4
- WPUINVXKIPAAHK-UHFFFAOYSA-N aluminum;potassium;oxygen(2-) Chemical compound [O-2].[O-2].[Al+3].[K+] WPUINVXKIPAAHK-UHFFFAOYSA-N 0.000 claims 1
- 229920000642 polymer Polymers 0.000 description 27
- 239000000839 emulsion Substances 0.000 description 13
- 239000000853 adhesive Substances 0.000 description 11
- 230000001070 adhesive effect Effects 0.000 description 11
- 230000000694 effects Effects 0.000 description 10
- 239000007864 aqueous solution Substances 0.000 description 7
- 238000010276 construction Methods 0.000 description 6
- 239000002585 base Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 229910017053 inorganic salt Inorganic materials 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 229910002651 NO3 Inorganic materials 0.000 description 3
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 3
- -1 alkali metal rhodan salts Chemical class 0.000 description 3
- 150000004645 aluminates Chemical class 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- KVOIJEARBNBHHP-UHFFFAOYSA-N potassium;oxido(oxo)alumane Chemical compound [K+].[O-][Al]=O KVOIJEARBNBHHP-UHFFFAOYSA-N 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000002174 Styrene-butadiene Substances 0.000 description 2
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 2
- 150000001805 chlorine compounds Chemical class 0.000 description 2
- 239000013065 commercial product Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- IIPYXGDZVMZOAP-UHFFFAOYSA-N lithium nitrate Chemical compound [Li+].[O-][N+]([O-])=O IIPYXGDZVMZOAP-UHFFFAOYSA-N 0.000 description 2
- YIXJRHPUWRPCBB-UHFFFAOYSA-N magnesium nitrate Chemical compound [Mg+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O YIXJRHPUWRPCBB-UHFFFAOYSA-N 0.000 description 2
- 238000000691 measurement method Methods 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 239000011115 styrene butadiene Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- 229910001294 Reinforcing steel Inorganic materials 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical group [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- AZFNGPAYDKGCRB-XCPIVNJJSA-M [(1s,2s)-2-amino-1,2-diphenylethyl]-(4-methylphenyl)sulfonylazanide;chlororuthenium(1+);1-methyl-4-propan-2-ylbenzene Chemical compound [Ru+]Cl.CC(C)C1=CC=C(C)C=C1.C1=CC(C)=CC=C1S(=O)(=O)[N-][C@@H](C=1C=CC=CC=1)[C@@H](N)C1=CC=CC=C1 AZFNGPAYDKGCRB-XCPIVNJJSA-M 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910001514 alkali metal chloride Inorganic materials 0.000 description 1
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 229910001617 alkaline earth metal chloride Inorganic materials 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
- GJTDJAPHKDIQIQ-UHFFFAOYSA-L barium(2+);dinitrite Chemical compound [Ba+2].[O-]N=O.[O-]N=O GJTDJAPHKDIQIQ-UHFFFAOYSA-L 0.000 description 1
- 230000001680 brushing 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
- 159000000007 calcium salts Chemical class 0.000 description 1
- XFWJKVMFIVXPKK-UHFFFAOYSA-N calcium;oxido(oxo)alumane Chemical compound [Ca+2].[O-][Al]=O.[O-][Al]=O XFWJKVMFIVXPKK-UHFFFAOYSA-N 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- HDERJYVLTPVNRI-UHFFFAOYSA-N ethene;ethenyl acetate Chemical group C=C.CC(=O)OC=C HDERJYVLTPVNRI-UHFFFAOYSA-N 0.000 description 1
- 235000010944 ethyl methyl cellulose Nutrition 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- YQNQTEBHHUSESQ-UHFFFAOYSA-N lithium aluminate Chemical compound [Li+].[O-][Al]=O YQNQTEBHHUSESQ-UHFFFAOYSA-N 0.000 description 1
- 229910000032 lithium hydrogen carbonate Inorganic materials 0.000 description 1
- IDNHOWMYUQKKTI-UHFFFAOYSA-M lithium nitrite Chemical compound [Li+].[O-]N=O IDNHOWMYUQKKTI-UHFFFAOYSA-M 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- HQRPHMAXFVUBJX-UHFFFAOYSA-M lithium;hydrogen carbonate Chemical compound [Li+].OC([O-])=O HQRPHMAXFVUBJX-UHFFFAOYSA-M 0.000 description 1
- AAJBNRZDTJPMTJ-UHFFFAOYSA-L magnesium;dinitrite Chemical compound [Mg+2].[O-]N=O.[O-]N=O AAJBNRZDTJPMTJ-UHFFFAOYSA-L 0.000 description 1
- 229920003087 methylethyl cellulose Polymers 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- RAFRTSDUWORDLA-UHFFFAOYSA-N phenyl 3-chloropropanoate Chemical compound ClCCC(=O)OC1=CC=CC=C1 RAFRTSDUWORDLA-UHFFFAOYSA-N 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 239000011433 polymer cement mortar Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229940068984 polyvinyl alcohol Drugs 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 239000004304 potassium nitrite Substances 0.000 description 1
- 235000010289 potassium nitrite Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- KUKFKAPJCRZILJ-UHFFFAOYSA-N prop-2-enenitrile;prop-2-enoic acid Chemical compound C=CC#N.OC(=O)C=C KUKFKAPJCRZILJ-UHFFFAOYSA-N 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010257 thawing Methods 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
Description
本発明は、断面修復工法等で、セメントコンクリートを打ち継ぐ際の接着性の向上を目的として使用するプライマー組成物、プライマー、及びそれを用いたプライマー処理方法に関する。 The present invention relates to a primer composition, a primer, and a primer treatment method using the primer composition, which are used for the purpose of improving adhesiveness when cement concrete is handed over by a cross-section repair method or the like.
土木・建築分野におけるポリマーディスパージョンの用途の1つとしてプライマーがある。
プライマーとは、コンクリートなどの下地に塗布することによって、その上に打設したモルタルなどと、コンクリートなどの下地との付着強度を向上させる効果を有するものである。
One of the uses of polymer dispersions in the field of civil engineering and construction is a primer.
The primer has an effect of improving the adhesion strength between a mortar placed on the base such as concrete and the base such as concrete by applying to the base such as concrete.
近年、コンクリート構造物は、塩害、中性化、凍結融解、及び化学的腐食等の作用により劣化が進行し、表面にひび割れや浮きなどが発生することが急増している。
その対策として、劣化した部分を打音検査等で確認し、電動ピック、エアピック、及びウォータージェットなどにより取り除き、耐久性に優れた補修モルタルなどの補修部材を充填し補修する工事が多く行われている。
In recent years, deterioration of concrete structures has progressed due to the effects of salt damage, neutralization, freezing and thawing, chemical corrosion, and the like, and the occurrence of cracks and floats on the surface is rapidly increasing.
As countermeasures, many repairs such as repairing parts such as repair mortar with excellent durability are carried out by checking the deteriorated part by hammering inspection, removing it with an electric pick, air pick, water jet, etc. Yes.
その際に、新たに施工した補修モルタルなどと、コンクリートなどの下地との付着強度を向上させる目的で、プライマーが使用されている。 At that time, a primer is used for the purpose of improving the adhesion strength between the newly-constructed repair mortar and the like and the groundwork such as concrete.
プライマーとして、酢酸ビニル−エチレン共重合体エマルジョンや、酢酸ビニル重合体エマルジョン、アクリル酸エステル重合体エマルジョン、これらの共重合体エマルジョン、及びこれらの混合エマルジョンを使用することが提案されており、いずれも接着力が向上する効果を得ているが、無機塩類を含有させることについては示されていない(特許文献1、特許文献2参照)。 It has been proposed to use a vinyl acetate-ethylene copolymer emulsion, a vinyl acetate polymer emulsion, an acrylate polymer emulsion, a copolymer emulsion thereof, or a mixed emulsion thereof as a primer. Although the effect which the adhesive force improves is obtained, it is not shown about containing an inorganic salt (refer patent document 1 and patent document 2).
また、低温環境下や低湿度で強い風が吹く季節での施工においても、接着面で打ち継ぐモルタルの硬化が促進するので接着力が低下しないという効果を得るために、最低造膜温度が10℃以下のエチレン性不飽和化合物の重合体水性エマルジョンと、アルカリ金属の塩化物、アルカリ土類金属の塩化物、亜鉛族元素の塩化物、鉄族元素の塩化物、アルカリ金属のケイ酸塩、アルカリ金属のロダン塩、及びアルカリ土類金属のロダン塩からなる群より選ばれる水溶性無機塩からなる組成物をプライマーとして使用することが提案されている(特許文献3参照)。
しかしながら、使用する水溶性無機塩が塩化物の場合は、塩化物イオンが浸透しコンクリート内部の鉄筋を錆びさせる可能性があり、ケイ酸塩の場合は塗布しすぎると厚い膜が形成し付着強度を低下させるという課題があった。
In addition, even in the construction in a low temperature environment or in a season where strong wind blows at low humidity, the hardening of the mortar to be inherited on the adhesive surface is accelerated, so that the adhesive strength does not decrease. Polymer aqueous emulsions of ethylenically unsaturated compounds below ℃ and alkali metal chlorides, alkaline earth metal chlorides, zinc group element chlorides, iron group element chlorides, alkali metal silicates, It has been proposed to use, as a primer, a composition comprising a water-soluble inorganic salt selected from the group consisting of alkali metal rhodan salts and alkaline earth metal rhodan salts (see Patent Document 3).
However, if the water-soluble inorganic salt used is chloride, chloride ions may permeate and rust the reinforcing steel inside the concrete. There was a problem of lowering.
さらに、エチレン−酢酸ビニル系エマルジョン、スチレン−ブタジエン系エマルジョン、及びアクリル酸エステル系エマルジョンよりも接着性が高く、耐アルカリ性等の耐久性も高い、エポキシ系のプライマーを使用することが提案されている(特許文献4参照)。
しかしながら、このエポキシ系のプライマーは、他のプライマーに比べ人体に対する刺激性が高く、噴霧によるプライマー処理作業が困難となるなどの課題があった。
Furthermore, it has been proposed to use an epoxy-based primer that has higher adhesion than ethylene-vinyl acetate emulsion, styrene-butadiene emulsion, and acrylate emulsion, and has high durability such as alkali resistance. (See Patent Document 4).
However, this epoxy primer has a problem that it is highly irritating to the human body compared to other primers, and the primer treatment work by spraying becomes difficult.
このように、エマルジョン系のプライマーの場合には、天井部の施工では厚くモルタルを塗ると自重により落下しやすくなったり、充分な付着強度が得られないなどといった課題があり、エポキシ系のプライマーの場合には、充分な付着強度を得やすいが、大断面の施工では噴霧による作業ができず、刷毛やローラー塗りで施工する必要があり時間を要するといった課題があった。
本発明者は、前記課題を解決するために種々検討した結果、特定のプライマー組成物を用いることで前記課題が解決できるという知見を得て本発明を完成するに至った。
In this way, in the case of emulsion-based primers, there are problems such as falling easily due to their own weight if the mortar is thickly applied in the ceiling construction, and sufficient adhesion strength cannot be obtained. In some cases, it is easy to obtain sufficient adhesion strength, but in the construction of a large cross section, the work by spraying cannot be performed, and there is a problem that it is necessary to perform construction by brushing or roller coating, which takes time.
As a result of various studies to solve the above problems, the present inventors have obtained the knowledge that the above problems can be solved by using a specific primer composition, and have completed the present invention.
即ち、本発明は、ポリマーディスパージョンと、アルミン酸カリウム、炭酸リチウム、及び硝酸カルシウムからなる群より選ばれた一種又は二種以上の無機塩類や硫酸アルミニウムとを含有してなり、無機塩類や硫酸アルミニウムが、固形分換算のポリマーディスパージョン100部に対して、2〜100部である、下地のセメントコンクリートと補修モルタルとの付着強度を向上させるプライマー組成物であり、さらに、増粘剤を含有する該プライマー組成物であり、該プライマー組成物を含有するプライマーであり、そのプライマー処理方法である。 That is, the present invention comprises a polymer dispersion and one or more inorganic salts selected from the group consisting of potassium aluminate, lithium carbonate, and calcium nitrate, and aluminum sulfate. aluminum, the polymer dispersion 100 parts of solid basis, 2 to 100 parts, a primer composition to improve the adhesion strength between the repair mortar and cement concrete foundation, is La, thickener A primer composition containing the primer composition, a primer containing the primer composition, and a primer treatment method thereof.
以下、本発明を詳細に説明する。
なお、本発明でいうセメントコンクリートとは、ペースト、モルタル、及びコンクリートを総称するものである。
また、本発明では特に限定しない限り部や%は質量基準である。
Hereinafter, the present invention will be described in detail.
In addition, the cement concrete as used in this invention is a general term for paste, mortar, and concrete.
In the present invention, unless otherwise specified, parts and% are based on mass.
本発明で使用するポリマーディスパージョン(以下、本ポリマーという)は特に限定されるものではないが、JIS A 6203に規定されているセメント混和剤ポリマーディスパージョン、例えば、アクリロニトリル−ブタジエンゴム、スチレン−ブタジエンゴム、クロロプレンゴム、及び天然ゴムなどのゴムラテックスや、エチレン−酢酸ビニル共重合体、ポリアクリル酸エステル、酢酸ビニルビニルバーサテート系共重合体、及びスチレン−アクリル酸エステル共重合体やアクリロニトリル−アクリル酸エステルに代表されるアクリル酸エステル系共重合体等の樹脂エマルジョンなどが挙げられる。 The polymer dispersion used in the present invention (hereinafter referred to as the present polymer) is not particularly limited, but is a cement admixture polymer dispersion defined in JIS A 6203, such as acrylonitrile-butadiene rubber, styrene-butadiene. Rubber latex such as rubber, chloroprene rubber, and natural rubber, ethylene-vinyl acetate copolymer, polyacrylate ester, vinyl acetate vinyl versatate copolymer, styrene-acrylate ester copolymer, and acrylonitrile-acrylic Examples thereof include resin emulsions such as acrylic ester copolymers typified by acid esters.
本発明では、本ポリマーと、アルミン酸塩、炭酸塩、及び硝酸塩からなる群より選ばれた一種又は二種以上の無機塩類、又は本ポリマーと硫酸アルミニウムとを併用するものである。
本発明において、無機塩類や硫酸アルミニウムは、いずれもセメントの凝結を促進するもので、本ポリマーと混合して、あるいは別々にセメントコンクリートなどの下地に、処理することが可能である。
In the present invention, the present polymer and one or more inorganic salts selected from the group consisting of aluminate, carbonate and nitrate, or the present polymer and aluminum sulfate are used in combination.
In the present invention, inorganic salts and aluminum sulfate all promote the coagulation of cement, and can be mixed with the present polymer or separately on a base such as cement concrete.
アルミン酸塩としては特に限定されるものではないが、具体的には、アルミン酸リチウム、アルミン酸ナトリウム、アルミン酸カリウム、及びアルミン酸カルシウムなどが挙げられる。 The aluminate is not particularly limited, and specific examples include lithium aluminate, sodium aluminate, potassium aluminate, and calcium aluminate.
炭酸塩としては特に限定されるものではないが、具体的には、炭酸リチウム、炭酸ナトリウム、炭酸カリウム、炭酸水素リチウム、炭酸水素ナトリウム、及び炭酸水素カリウムなどが挙げられる。 Although it does not specifically limit as carbonate, Specifically, lithium carbonate, sodium carbonate, potassium carbonate, lithium hydrogencarbonate, sodium hydrogencarbonate, potassium hydrogencarbonate, etc. are mentioned.
硝酸塩としては、硝酸リチウム、硝酸ナトリウム、硝酸カリウム、硝酸カルシウム、硝酸マグネシウム、亜硝酸リチウム、亜硝酸ナトリウム、亜硝酸カリウム、亜硝酸カルシウム、亜硝酸マグネシウム、及び亜硝酸バリウムなどが挙げられる。 Examples of the nitrate include lithium nitrate, sodium nitrate, potassium nitrate, calcium nitrate, magnesium nitrate, lithium nitrite, sodium nitrite, potassium nitrite, calcium nitrite, magnesium nitrite, and barium nitrite.
これらの無機塩類のうち、アルカリ骨材反応に対して無害と考えられるリチウム塩やカルシウム塩の使用が好ましい。
無機塩類の使用量は、固形分換算の本ポリマー100部に対して、2〜100部であり、5〜50部が好ましい。2部未満ではセメントの凝結促進効果が小さく、付着力の向上効果が期待できない場合があり、100部を超えると付着力の向上効果が頭打ちとなる場合がある。
本発明で無機塩類は、あらかじめ粉体のまま又は水溶液として、本ポリマーと混合して使用することも可能であり、本ポリマーと別々に使用し、コンクリートなどの下地表面で混合することも可能である。
Of these inorganic salts, it is preferable to use lithium salts or calcium salts that are considered harmless to the alkali-aggregate reaction.
The usage-amount of inorganic salt is 2-100 parts with respect to 100 parts of this polymer of solid content conversion, and 5-50 parts is preferable. If the amount is less than 2 parts, the effect of promoting the setting of cement is small, and the effect of improving the adhesive strength may not be expected.
In the present invention, inorganic salts can be used in the form of a powder or as an aqueous solution and mixed with the present polymer. Alternatively, the inorganic salts can be used separately from the present polymer and mixed on the ground surface of concrete or the like. is there.
本発明では、セメントの凝結を促進するために無機塩類の代わりに硫酸アルミニウムを使用することが可能である。
硫酸アルミニウムの使用量は、固形分換算の本ポリマー100部に対して、2〜100部であり、5〜50部が好ましい。2部未満ではセメントの凝結促進効果が小さく、付着力の向上効果が期待できない場合があり、100部を超えると付着力の向上効果が頭打ちとなる場合がある。
In the present invention, it is possible to use aluminum sulfate in place of inorganic salts in order to promote cement setting.
The usage-amount of aluminum sulfate is 2-100 parts with respect to 100 parts of this polymer of solid content conversion, and 5-50 parts is preferable. If the amount is less than 2 parts, the effect of promoting the setting of cement is small, and the effect of improving the adhesive strength may not be expected.
本発明では、プライマー組成物の粘性を増加させ、使用したときのダレを防止したり、モルタルやコンクリートの接着面での粘着力を増加させる目的で、さらに、増粘剤を使用することが好ましい。
増粘剤としては特に限定されるものではないが、メチルセルロース、メチルエチルセルロース、ヒドロキシプロピルセルロース、ヒドロキシプロピルメチルセルロース、ヒドロキシエチルセルロース、及びカルボキシメチルセルロースなどセルロース類又はその塩、ポリアクリルアミドやその変成物、ポリアクリルアミド部分加水分解物、ポリアクリル酸ソーダやアルギン酸ソーダ、ポリビニルアルコール、並びに、グアーガムやキサンタンガムなどが挙げられる。
増粘剤の使用量は、固形分換算の本ポリマー100部に対して、0.02〜2部が好ましく、0.05〜1部がより好ましい。0.02部未満ではダレ防止やモルタルやコンクリートの粘着力向上が期待できない場合があり、2部を超えるとモルタルやコンクリートの粘着力向上が頭打ちとなる場合がある。
増粘剤の混合方法は、本ポリマーにあらかじめ混合しておくことが好ましいが、無機塩類又は硫酸アルミニウム(以下、無機塩類等という)の水溶液を調整するときはその水溶液に混合することも可能であり、無機塩類等の水溶液と本ポリマーいずれに混合することも可能である。
In the present invention, it is preferable to further use a thickener for the purpose of increasing the viscosity of the primer composition, preventing dripping when used, or increasing the adhesive force on the adhesive surface of mortar or concrete. .
The thickening agent is not particularly limited, but celluloses such as methylcellulose, methylethylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose, hydroxyethylcellulose, and carboxymethylcellulose or salts thereof, polyacrylamide and its modified products, polyacrylamide moiety Examples include hydrolysates, sodium polyacrylate, sodium alginate, polyvinyl alcohol, and guar gum and xanthan gum.
The amount of thickener used is preferably 0.02 to 2 parts, more preferably 0.05 to 1 part, based on 100 parts of the present polymer in terms of solid content. If it is less than 0.02 part, dripping prevention and improvement in adhesive strength of mortar and concrete may not be expected. If it exceeds 2 parts, improvement in adhesive strength of mortar and concrete may reach its peak.
The thickener is preferably mixed in advance with the polymer, but when preparing an aqueous solution of inorganic salts or aluminum sulfate (hereinafter referred to as inorganic salts), it can also be mixed with the aqueous solution. Yes, it can be mixed with an aqueous solution of inorganic salts and the present polymer.
本発明のプライマー組成物は、固形分換算の本ポリマー100部に対して、水100〜600部加え希釈して使用することが好ましい。本ポリマーの固形分濃度が高すぎると下地への浸透効果が得にくい場合がある。
また、無機塩類等を水溶液として使用する場合は、本ポリマーと混合した際、水が、固形分換算の本ポリマー100部に対して、100〜600部となるように調整することが好ましい。
The primer composition of the present invention is preferably used by diluting 100 to 600 parts of water with respect to 100 parts of the present polymer in terms of solid content. If the solid content concentration of the polymer is too high, it may be difficult to obtain the effect of penetrating into the base.
Moreover, when using inorganic salts etc. as aqueous solution, when mixing with this polymer, it is preferable to adjust so that water may be 100-600 parts with respect to 100 parts of this polymer of solid content conversion.
本発明のプライマー組成物の使用量は、塗布あるいは噴霧する面1m2に対して、50〜1,000gが好ましく、100〜600gがより好ましい。50g未満では接着力向上効果が得られない場合があり、1,000gを超えると接着力向上効果が頭打ちとなる場合がある。 The use amount of the primer composition of the present invention is preferably 50 to 1,000 g, more preferably 100 to 600 g, per 1 m 2 of the surface to be coated or sprayed. If it is less than 50 g, the effect of improving the adhesive strength may not be obtained, and if it exceeds 1,000 g, the effect of improving the adhesive strength may reach its peak.
本発明のプライマー組成物のプライマー処理方法は特に限定されるものではないが、刷毛やローラーを用いて表面に塗布する方法や、霧吹きや加圧散布器等を用いて噴霧する方法のいずれも可能である。
また、ポリマーディスパージョンにあらかじめ無機塩類等を混合したものを使用してもよく、無機塩類等を水溶液として、ポリマーディスパージョンと無機塩類等の水溶液を別々に塗布あるいは噴霧して使用することも可能である。
The primer treatment method of the primer composition of the present invention is not particularly limited, but any of a method of applying to a surface using a brush or a roller, or a method of spraying using a spray or a pressure sprayer is possible. It is.
In addition, polymer dispersions previously mixed with inorganic salts may be used, and inorganic salts can be used as aqueous solutions, and polymer dispersions and aqueous solutions such as inorganic salts can be applied or sprayed separately. It is.
本発明のプライマー組成物を使用することで、早期に付着強度を得ることが可能となり、天井面の施工においても、補修モルタルを厚付けしても剥落がなく充分な付着強度を得ることが可能となる。 By using the primer composition of the present invention, it becomes possible to obtain adhesion strength at an early stage, and even in the construction of the ceiling surface, it is possible to obtain sufficient adhesion strength without peeling even if the repair mortar is thickened. It becomes.
以下、実施例に基づき本発明を詳細に説明する。 Hereinafter, the present invention will be described in detail based on examples.
固形分換算の本ポリマー100部に対して、表1に示す無機塩類等を混合してプライマー組成物とし、さらに、水200部と混合してプライマーを調製した。
サンドペーパーで研磨処理したモルタル硬化体の面を下地とし、表面に、調製したプライマー300g/m2を塗布し、補修モルタルをコテで塗り付けて、2日後に付着強度を測定した。結果を表1に併記する。
To 100 parts of this polymer in terms of solid content, inorganic salts shown in Table 1 were mixed to obtain a primer composition, and further mixed with 200 parts of water to prepare a primer.
The surface of the mortar cured body polished with sandpaper was used as a base, the prepared primer 300 g / m 2 was applied to the surface, the repair mortar was applied with a trowel, and the adhesion strength was measured after 2 days. The results are also shown in Table 1.
<使用材料>
無機塩類等a:アルミン酸塩、アルミン酸カリウム、試薬1級
無機塩類等b:炭酸塩、炭酸リチウム、試薬1級
無機塩類等c:硝酸塩、硝酸カルシウム、試薬1級
本ポリマーA:エチレン−酢酸ビニル系エマルジョン、固形分濃度45%
本ポリマーB:アクリル酸エステル−アクリロニトリル系エマルジョン、固形分濃度45%
補修モルタル:コテ塗り用ポリマーセメントモルタル、市販品
<Materials used>
Inorganic salts, etc. a: aluminate, potassium aluminate, reagent primary inorganic salts, etc. b: carbonate, lithium carbonate, reagent primary inorganic salts, etc. c: nitrate, calcium nitrate, reagent primary, main polymer A: ethylene-acetic acid Vinyl emulsion, solid concentration 45%
This polymer B: acrylate-acrylonitrile emulsion, solid content concentration 45%
Repair mortar: Polymer cement mortar for iron coating, commercial product
<測定方法>
付着強度 :JIS A 1171に準拠し、建研式引抜試験機で測定
<Measurement method>
Adhesion strength: Measured with a Kenken-type pull-out tester in accordance with JIS A 1171
固形分換算の本ポリマー100部に対して、表2に示す無機塩類等dを使用し、プライマー組成物としたこと以外は実施例1と同様に行った。結果を表2に併記する。 The same procedure as in Example 1 was performed except that 100 parts of this polymer in terms of solid content was used as a primer composition using d such as inorganic salts shown in Table 2. The results are also shown in Table 2.
<使用材料>
無機塩類等d:硫酸アルミニウム、試薬1級
<Materials used>
Inorganic salts d: Aluminum sulfate, reagent grade 1
固形分換算の本ポリマーA100部に対して、無機塩類等c20部と表3に示す増粘剤を使用し、プライマー組成物としたこと以外は実施例1と同様に行った。結果を表3に併記する。 The same procedure as in Example 1 was performed except that c20 parts of inorganic salts and the thickener shown in Table 3 were used as a primer composition with respect to 100 parts of this polymer A in terms of solid content. The results are also shown in Table 3.
<使用材料>
増粘剤 :メチルセルロース、市販品
<Materials used>
Thickener: methylcellulose, commercial product
固形分換算の本ポリマーA100部に対して、無機塩類等c20部と表4に示す増粘剤を使用し、プライマー組成物とし、表4に示す量のプライマーを塗布したこと以外は実施例1と同様に行った。結果を表4に併記する。 Example 1 except that c20 parts of inorganic salts and the thickener shown in Table 4 were used for 100 parts of this polymer A in terms of solid content, and the primer composition was applied as a primer composition in the amount shown in Table 4. As well as. The results are also shown in Table 4.
本ポリマーA100部に対して、表5に示す無機塩類等と増粘剤とを混合してプライマー組成物とし、さらに水200部を混合してプライマーを調製した。
縦30cm×横30cm×厚さ6cmのサンドブラストしたコンクリート板を天井面に取り付け、その表面に、調製したプライマーを300g/m2となるように噴霧し、厚さ7cmとなるように一回で補修モルタルを塗り付けた。その時の塗り付けた補修モルタルの安定性と7日後の付着強度を測定した。結果を表5に併記する。
To 100 parts of this polymer A, inorganic salts shown in Table 5 and a thickener were mixed to obtain a primer composition, and 200 parts of water was further mixed to prepare a primer.
A 30cm long x 30cm wide x 6cm thick sandblasted concrete board is attached to the ceiling surface, and the prepared primer is sprayed on the surface to 300g / m 2 and repaired once to a thickness of 7cm. Mortar was applied. The stability of the repaired mortar applied at that time and the adhesion strength after 7 days were measured. The results are also shown in Table 5.
<測定方法>
安定性 :7cm塗り付けることができない、又は、塗り付けられても1日後剥落するようであれば×、1日後でもモルタルが剥落せずに付着していれば○とした。
付着強度 :塗り付けて2日後に内径55mmのコアドリルで下地コンクリート板から深さ5mm程度まで削孔したものを付着強度試験用供試体とし、5日間、温度60%の恒温恒湿で気中養生し、建研式引抜試験機を用いて測定。
<Measurement method>
Stability: If 7 cm cannot be applied, or even if it is applied, it will be peeled off after 1 day. If the mortar is not peeled off even after 1 day, it will be marked as ◯.
Adhesion strength: Two days after application, a core drill with an inner diameter of 55 mm drilled from the ground concrete plate to a depth of about 5 mm was used as a test specimen for the adhesion strength test for 5 days at 60% temperature and humidity. Measured using a Kenken pull-out tester.
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Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS5038404B2 (en) * | 1971-11-19 | 1975-12-09 | ||
JPH05222321A (en) * | 1992-02-07 | 1993-08-31 | Nippon Paint Co Ltd | Water-base primer composition for treating substrate consisting of aluminum or its alloy |
JPH06340462A (en) * | 1992-10-23 | 1994-12-13 | Sansou:Kk | Fiber reinforced cement composite material |
JPH08283059A (en) * | 1995-04-06 | 1996-10-29 | Nippon Cement Co Ltd | Composition for base preparation |
JP2000248381A (en) * | 1999-02-26 | 2000-09-12 | Nippon Light Metal Co Ltd | Hydrophilic treating method for aluminum material, substrate treating agent and hydrophilic coating material therefor |
JP2002356357A (en) * | 2001-05-31 | 2002-12-13 | Taiheiyo Material Kk | Mortar |
JP2003129670A (en) * | 2001-10-22 | 2003-05-08 | Denki Kagaku Kogyo Kk | Spray repair method |
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Publication number | Priority date | Publication date | Assignee | Title |
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JPS5038404B2 (en) * | 1971-11-19 | 1975-12-09 | ||
JPH05222321A (en) * | 1992-02-07 | 1993-08-31 | Nippon Paint Co Ltd | Water-base primer composition for treating substrate consisting of aluminum or its alloy |
JPH06340462A (en) * | 1992-10-23 | 1994-12-13 | Sansou:Kk | Fiber reinforced cement composite material |
JPH08283059A (en) * | 1995-04-06 | 1996-10-29 | Nippon Cement Co Ltd | Composition for base preparation |
JP2000248381A (en) * | 1999-02-26 | 2000-09-12 | Nippon Light Metal Co Ltd | Hydrophilic treating method for aluminum material, substrate treating agent and hydrophilic coating material therefor |
JP2002356357A (en) * | 2001-05-31 | 2002-12-13 | Taiheiyo Material Kk | Mortar |
JP2003129670A (en) * | 2001-10-22 | 2003-05-08 | Denki Kagaku Kogyo Kk | Spray repair method |
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