JPH0331340A - Asphalt emulsion - Google Patents
Asphalt emulsionInfo
- Publication number
- JPH0331340A JPH0331340A JP16635489A JP16635489A JPH0331340A JP H0331340 A JPH0331340 A JP H0331340A JP 16635489 A JP16635489 A JP 16635489A JP 16635489 A JP16635489 A JP 16635489A JP H0331340 A JPH0331340 A JP H0331340A
- Authority
- JP
- Japan
- Prior art keywords
- emulsion
- asphalt
- asphalt emulsion
- rubber
- acid compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000839 emulsion Substances 0.000 title claims abstract description 70
- 239000010426 asphalt Substances 0.000 title claims abstract description 65
- -1 acrylic acid compound Chemical class 0.000 claims abstract description 25
- 229920000126 latex Polymers 0.000 claims abstract description 24
- 229920001971 elastomer Polymers 0.000 claims abstract description 15
- 239000005060 rubber Substances 0.000 claims abstract description 15
- 239000007787 solid Substances 0.000 claims abstract description 13
- 229920001577 copolymer Polymers 0.000 claims abstract description 12
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 125000000129 anionic group Chemical group 0.000 claims abstract description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 10
- 230000002378 acidificating effect Effects 0.000 claims abstract description 6
- 239000003054 catalyst Substances 0.000 claims abstract description 6
- 239000003513 alkali Substances 0.000 claims abstract description 5
- 238000002156 mixing Methods 0.000 abstract description 11
- 239000000463 material Substances 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 10
- 230000008023 solidification Effects 0.000 description 10
- 238000007711 solidification Methods 0.000 description 10
- 229920003048 styrene butadiene rubber Polymers 0.000 description 10
- 239000002174 Styrene-butadiene Substances 0.000 description 9
- 230000008439 repair process Effects 0.000 description 8
- 239000004816 latex Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 5
- 239000003945 anionic surfactant Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 230000009477 glass transition Effects 0.000 description 4
- 230000000379 polymerizing effect Effects 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000002685 polymerization catalyst Substances 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- NXQMCAOPTPLPRL-UHFFFAOYSA-N 2-(2-benzoyloxyethoxy)ethyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCCOCCOC(=O)C1=CC=CC=C1 NXQMCAOPTPLPRL-UHFFFAOYSA-N 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 2
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 2
- 239000004575 stone Substances 0.000 description 2
- VDYWHVQKENANGY-UHFFFAOYSA-N 1,3-Butyleneglycol dimethacrylate Chemical compound CC(=C)C(=O)OC(C)CCOC(=O)C(C)=C VDYWHVQKENANGY-UHFFFAOYSA-N 0.000 description 1
- NMMHHKWLQMFEDM-UHFFFAOYSA-N 2-(9-pentylheptadecan-9-yloxycarbonyl)benzoic acid Chemical compound CCCCCCCCC(CCCCC)(CCCCCCCC)OC(=O)C1=CC=CC=C1C(=O)O NMMHHKWLQMFEDM-UHFFFAOYSA-N 0.000 description 1
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 1
- DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 description 1
- LTHJXDSHSVNJKG-UHFFFAOYSA-N 2-[2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOCCOC(=O)C(C)=C LTHJXDSHSVNJKG-UHFFFAOYSA-N 0.000 description 1
- FWWXYLGCHHIKNY-UHFFFAOYSA-N 2-ethoxyethyl prop-2-enoate Chemical compound CCOCCOC(=O)C=C FWWXYLGCHHIKNY-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 description 1
- GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 1
- FIHBHSQYSYVZQE-UHFFFAOYSA-N 6-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCCOC(=O)C=C FIHBHSQYSYVZQE-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 239000004606 Fillers/Extenders Substances 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
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 1
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- BQSLMFSQEBXZHN-UHFFFAOYSA-N bis(8-methylnonyl) butanedioate Chemical compound CC(C)CCCCCCCOC(=O)CCC(=O)OCCCCCCCC(C)C BQSLMFSQEBXZHN-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 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
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- 238000011038 discontinuous diafiltration by volume reduction Methods 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- DWXAVNJYFLGAEF-UHFFFAOYSA-N furan-2-ylmethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1=CC=CO1 DWXAVNJYFLGAEF-UHFFFAOYSA-N 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000010903 husk Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- WIBFFTLQMKKBLZ-SEYXRHQNSA-N n-butyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCCC WIBFFTLQMKKBLZ-SEYXRHQNSA-N 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
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- MUTNCGKQJGXKEM-UHFFFAOYSA-N tamibarotene Chemical compound C=1C=C2C(C)(C)CCC(C)(C)C2=CC=1NC(=O)C1=CC=C(C(O)=O)C=C1 MUTNCGKQJGXKEM-UHFFFAOYSA-N 0.000 description 1
- SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- KEROTHRUZYBWCY-UHFFFAOYSA-N tridecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCOC(=O)C(C)=C KEROTHRUZYBWCY-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Road Paving Structures (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
[発明の目的]
(産業上の利用分野)
本発明は、コンクリートや、アスファルト舗装道路の亀
裂補修等に適したアスファルト系エマルジョンに関する
。Detailed Description of the Invention [Object of the Invention] (Industrial Application Field) The present invention relates to an asphalt-based emulsion suitable for repairing cracks in concrete and asphalt-paved roads.
(従来の技術)
従来よりアスファルト舗装道路の亀裂補修には、一般に
溶融アスファルトやゴムラテックスを混合した溶融アス
ファルト、あるいはアスファルト乳剤を流し込むという
方法がとられている。(Prior Art) Conventionally, cracks in asphalt-paved roads have been repaired by pouring molten asphalt, molten asphalt mixed with rubber latex, or asphalt emulsion.
しかしながら、この方法によると、亀裂部に入った溶融
アスファルトは、直ちに冷却されて固化してしまうため
亀裂の先端部にまで充填できず、道路の表面付近だけを
塞いだ形になっているため補修部分の強度が弱く、再度
亀裂が生じやすい。However, with this method, the molten asphalt that enters the crack immediately cools and solidifies, making it impossible to fill the tip of the crack, leaving only the area near the surface of the road closed. The strength of the parts is weak and cracks are likely to occur again.
また、使用できる温度範囲が一り5℃〜35℃程度と狭
いため、夏期には溶融しやすく寒冷地では亀裂を生じや
すい。さらに、ゴムラテックスを混合した溶融アスファ
ルトは、100℃程度に熱したアスファルトをゴムラテ
ックス中に少量ずつ滴下する製法を経るため作業性が悪
いうえに、粘着性のある高温物質であるので、作業者に
およぼす危険性も高いという欠点を有している。Furthermore, since the temperature range in which it can be used is narrow, from about 5°C to 35°C, it tends to melt in the summer and easily cracks in cold regions. Furthermore, molten asphalt mixed with rubber latex is manufactured by dropping asphalt heated to about 100°C into the rubber latex little by little, making it difficult to work with. It also has the disadvantage of being highly dangerous.
さらにまた、アスファルト乳剤は、硬化に1週間以上を
要し、かつ水分が約50重量%を占めるため硬化後の体
積減少が著しく、再度補修を必要とする場合も多く、ま
た、流動温度が低いため、わだち掘れ等を生じやすい。Furthermore, asphalt emulsions require more than a week to harden, and since the water content is about 50% by weight, the volume decreases significantly after hardening, often requiring repair, and the flow temperature is low. Therefore, rutting etc. are likely to occur.
一方、建物やトンネル、地下道等におけるコンクリート
の亀裂補修や、コンクリートと、鋼材の結合剤としては
、従来からコンクリート、コンクリートミルク、コンク
リートと樹脂の混合物等が使用されているが、これらは
乾燥に多くの時間がかかるという問題がある。On the other hand, concrete, concrete milk, mixtures of concrete and resin, etc. have traditionally been used for repairing cracks in concrete in buildings, tunnels, underpasses, etc., and as binding agents for concrete and steel, but these are often used for drying purposes. The problem is that it takes time.
さらに近年ではアスファルト乳剤にゴムラテックスを配
合したアスファルト舗装用亀裂補修材が提案されている
が、この補修材は乾燥固化が水分の蒸発による自然放置
の場合には非常に長い時間を要し、早く乾燥させるため
には加熱により脱水乾燥を促進する必要があるという欠
点を有している。また、補修材の厚さが厚い場合には表
面のみが固まって内部が固まらず、さらに乾燥後の体積
減少が大きいうえに、熱や紫外線による劣化が激しく耐
候性に劣るという欠点がある。Furthermore, in recent years, crack repair materials for asphalt pavement have been proposed that are made by blending rubber latex with asphalt emulsion. It has the disadvantage that in order to dry it, it is necessary to accelerate dehydration and drying by heating. In addition, if the repair material is thick, only the surface hardens and the inside does not harden, and furthermore, there is a large volume reduction after drying, and there are drawbacks such as severe deterioration due to heat and ultraviolet rays and poor weather resistance.
上記のような汎用止水材の他に、シリコーン系止水材、
エポキシ系■ヒ水材、吸水性ポリマー系止水材、あるい
はアスファルトを特定の有機溶剤に溶解してなるカット
バックアスファルト等が止水材、亀裂補修剤として用い
られるが、シリコーン系止水材、エポキシ系止水材は浸
透性が悪く亀裂の先端まで充填できないこと、接着性に
劣ること、コスト高であること等の欠点を有し、吸水性
ポリマー系止水材はゲル状に硬化するので極めて脆く、
耐寒性、耐熱性に劣る等の欠点を有し、さらにカットバ
ックアスファルトは耐寒性、耐熱性に劣る等の欠点を有
している。In addition to the general-purpose water-stopping materials mentioned above, silicone-based waterstopping materials,
Epoxy-based water-stopping materials, water-absorbing polymer-based water-stopping materials, or cutback asphalt made by dissolving asphalt in a specific organic solvent are used as water-stopping materials and crack repair agents, but silicone-based water-stopping materials, Epoxy-based water-stopping materials have disadvantages such as poor permeability and inability to fill to the tip of cracks, poor adhesion, and high cost, while water-absorbing polymer-based waterstopping materials harden into a gel-like state. Extremely fragile;
It has drawbacks such as poor cold resistance and heat resistance, and furthermore, cutback asphalt has drawbacks such as poor cold resistance and heat resistance.
さらに、近年、カチオン性のアスファルト乳剤に、アク
リル酸またはメタクリル酸の重合体のカチオン性エマル
ジョンを混合して強度を向上させた補修材も開発されて
いるが、これは硬化速度が速過ぎて亀裂の先端部まで充
分に充填することができないうえに、エマルジョンの状
態が不安定で作業性がよくないという問題があった。Furthermore, in recent years, repair materials have been developed that improve strength by mixing cationic asphalt emulsions with cationic emulsions of acrylic acid or methacrylic acid polymers, but these repair materials cure too quickly and crack. There were problems in that it was not possible to fully fill the tip of the emulsion, and the state of the emulsion was unstable, resulting in poor workability.
このように、上水材、亀裂補修剤としては種々の材料が
提案されているが、未だ浸透性、耐寒性、高いゴム弾性
、適当な硬化速度等の諸特性を充分に満足するものが得
られていないのが現状である。As described above, various materials have been proposed as water supply materials and crack repair agents, but it is still difficult to find a material that fully satisfies various properties such as permeability, cold resistance, high rubber elasticity, and appropriate curing speed. The current situation is that this is not the case.
(発明が解決しようとする課題)
本発明は、亀裂の先端部にまで充填が可能で、かつゴム
弾性を高め、適用できる温度範囲を広げて寒冷地での使
用にも充分耐え得るとともに、浸透および作業に適当な
固化時間を有するアスファルト系エマルジョンを提供す
ることを目的とする。(Problems to be Solved by the Invention) The present invention enables filling up to the tips of cracks, increases rubber elasticity, expands the applicable temperature range, can withstand use in cold regions, and penetrates into cracks. The object of the present invention is to provide an asphalt emulsion having a solidification time suitable for the work.
[発明の構成]
(課題を解決するための手段)
本発明のアスファルト系エマルジョンは、(a)アスフ
ァルト乳剤および/またはゴム・アスファルト乳剤と、
(b)アクリル酸化合物および/またはメタクリル酸化
合物と酢酸ビニルとを酸性触媒の存在下で重合させ、ア
ルカリでpl+を7より大とした共重合体のアニオン性
エマルジッンとを、(a): (b)が99:1〜5
0:50の固形分重量比で混合し、またはこれにさらに
(c)ゴムラテックスを、(a): (b)+ (c
)が99+1〜70:30の固形分子f!ffi比とな
るよう混合してなることを特徴としている。[Structure of the Invention] (Means for Solving the Problems) The asphalt emulsion of the present invention comprises (a) an asphalt emulsion and/or a rubber/asphalt emulsion;
(b) An anionic emulsion of a copolymer obtained by polymerizing an acrylic acid compound and/or a methacrylic acid compound and vinyl acetate in the presence of an acidic catalyst and having a pl+ of greater than 7 with an alkali, (a): ( b) is 99:1-5
(a): (b) + (c
) is 99+1 to 70:30 solid molecule f! It is characterized by being mixed so that the ffi ratio is achieved.
まず、本発明に使用される(a)のアニオン性のアスフ
ァルト乳剤およびゴム・アスファルト乳剤について説明
する。(以下、ffi′量部および重量比はすべて固形
分換算である。)
アニオン性のアスファルト乳剤は、天然アスファルト、
石油アスファルトのようなアスファルトを溶融しこれを
アニオン系界面活性剤を用いて乳化させたもので、固化
までに充分な作業時間、浸透時間がとれ、補修作業がし
やすいという利点がある。アニオン性のゴム、アスファ
ルト乳剤としては、ゴムラテックス 100重2部(以
下、単に部と示す)に加熱溶融したアスファルト 10
0−1200部を配合し、さらにアニオン系界面活性剤
と分散安定剤を混合した含有水分量8〜35重量%(以
下、単に%と示す。)の高濃度エマルジョンが好適する
。上記の高濃度エマルジョンに使用されるゴムラテック
スとしては、S[3R、ビニルピリジンSBR。First, the anionic asphalt emulsion and rubber asphalt emulsion (a) used in the present invention will be explained. (Hereinafter, all ffi' parts and weight ratios are based on solid content.) The anionic asphalt emulsion is made of natural asphalt,
It is made by melting asphalt such as petroleum asphalt and emulsifying it using an anionic surfactant, which has the advantage of allowing sufficient working time and penetration time to solidify and making repair work easier. As an anionic rubber or asphalt emulsion, asphalt 100 parts by weight of rubber latex (hereinafter simply referred to as "parts") is heated and melted.
A high concentration emulsion containing 0 to 1200 parts of water and an anionic surfactant and a dispersion stabilizer with a water content of 8 to 35% by weight (hereinafter simply referred to as %) is suitable. The rubber latex used in the above high concentration emulsion is S[3R, vinylpyridine SBR.
カルボキシ変性SBI? 、NBRのラテックスがある
。Carboxy-modified SBI? , NBR latex is available.
また、アスファルトとしては天然アスファルト、石油ア
スファルトのいずれでもよく、これらの°ストレートア
スファルト、ブローンアスファルト、その他を単独また
は混合して使用する。これらのアスファルトのゴムラテ
ックスへの添加温度は、分散性やゴムラテックスの安定
性から、70〜150℃の範囲が好ましい。The asphalt may be either natural asphalt or petroleum asphalt, and straight asphalt, blown asphalt, and others may be used alone or in combination. The temperature at which these asphalts are added to the rubber latex is preferably in the range of 70 to 150°C from the viewpoint of dispersibility and stability of the rubber latex.
アニオン系界面活性剤としては脂肪酸塩、高級アルコー
ル硫酸エステル塩、アルキルベンゼンスルホン酸塩、ロ
ジン酸塩等がある。Examples of anionic surfactants include fatty acid salts, higher alcohol sulfate ester salts, alkylbenzene sulfonates, and rosinates.
分散安定剤としては、無機系ではベントナイト、クレー
等があり、有機系ではポリビニルアルコール、メチルセ
ルロース、ヒドロキシエチルセルロース、カルボキシメ
チルセルロース、ポリアクリル酸ソーダ、デンプン、カ
ゼイン等があり、単独または混合して使用することによ
り、得られるゴム・アスファルト乳剤の安定性を良好に
する。Dispersion stabilizers include inorganic ones such as bentonite and clay, and organic ones such as polyvinyl alcohol, methyl cellulose, hydroxyethyl cellulose, carboxymethyl cellulose, sodium polyacrylate, starch, and casein, which can be used alone or in combination. This improves the stability of the resulting rubber/asphalt emulsion.
本発明のアクリル酸化合物および/またはメタクリル酸
化合物と酢酸ビニルとの共重合体のアニオン性エマルジ
ョンは、これらの化合物と水と乳化剤との混合液に過硫
酸アンモニウムのような酸性触媒を添加して温水中で攪
拌することにより重合させ、次いでアンモニア水のよう
なアル号りで中和してpiを7より大として反応を停止
させることにより得られる。The anionic emulsion of a copolymer of an acrylic acid compound and/or a methacrylic acid compound and vinyl acetate of the present invention can be produced by adding an acidic catalyst such as ammonium persulfate to a mixture of these compounds, water, and an emulsifier, and then adding an acidic catalyst such as ammonium persulfate to the mixture with hot water. It can be obtained by polymerizing by stirring in an aqueous solution, followed by neutralization with alkali such as aqueous ammonia to make pi greater than 7 and stopping the reaction.
アクリル酸化合物およびメタクリル酸化合物としては、
アクリル酸、アクリル酸エステル、ポリアクリル酸ソー
ダ、アクリル酸塩類モノマー アクリル酸ジメチルアミ
ノエチルエステル、アクリル酸イソブチル、アクリル酸
ジエチレングリコールエトキシレート、2−エトキシエ
チルアクリレート、エポキシアクリレート、n−エステ
ルアクリレート、テトラヒドロフルフリルアクリレート
、トリメチロールプロパントリアクリレート、2−ヒド
ロキシエチルアクリレート、2−ヒドロキシプロピルア
クリレート、1.4−ブタンジオールジアクリレート、
1,6−ヘキサンジオールジアクリレート、ペンタエリ
スリトールトリアクリレート、ラウリル−トリデシル(
混合)アクリレート、メチルメタクリレート(メタクリ
ル酸t−ブチル、メタクリル酸2−エチルヘキシル、メ
タクリル酸トリデシル、メタクリル酸ステアリル、゛メ
タクリル酸シクロヘキシル、メタクリル酸、メタクリル
酸2−ヒドロキシプロピル、メタクリル酸ジメチルアミ
ノエチル、テトラヒトメタクリル酸フルフリル、ジメタ
クリル酸エチレン、ジメタクリル酸テトラエチレングリ
コール、ジメタクリル酸1,3・−ブチレン、トリメタ
クリル酸トリメチロールプロパン、グリシジルメタクリ
レート、n−プチルメタクリレート、インブチルメタク
リレート、2−ヒドロキシエチルメタクリレート、ラウ
リルメタクリレート等がある。As acrylic acid compounds and methacrylic acid compounds,
Acrylic acid, acrylic acid ester, sodium polyacrylate, acrylate monomers dimethylaminoethyl acrylate, isobutyl acrylate, diethylene glycol ethoxylate acrylate, 2-ethoxyethyl acrylate, epoxy acrylate, n-ester acrylate, tetrahydrofurfuryl acrylate, trimethylolpropane triacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, 1,4-butanediol diacrylate,
1,6-hexanediol diacrylate, pentaerythritol triacrylate, lauryl-tridecyl (
Mixed) acrylate, methyl methacrylate (t-butyl methacrylate, 2-ethylhexyl methacrylate, tridecyl methacrylate, stearyl methacrylate, cyclohexyl methacrylate, methacrylic acid, 2-hydroxypropyl methacrylate, dimethylaminoethyl methacrylate, tetrahedron) Furfuryl methacrylate, ethylene dimethacrylate, tetraethylene glycol dimethacrylate, 1,3-butylene dimethacrylate, trimethylolpropane trimethacrylate, glycidyl methacrylate, n-butyl methacrylate, inbutyl methacrylate, 2-hydroxyethyl methacrylate , lauryl methacrylate, etc.
共重合させる各化合物の重量比は、アクリル酸化合物お
よび/またはメタクリル酸化合物:酢酸ビニル(モノマ
ー)■10:90〜90:10の範囲が好ましく、酢酸
ビニル゛成分がこれより多いとポリ酢酸ビニル部分が多
くなるため得られる固化物の硬度が充分でなくなる。逆
に酢酸ビニル成分がこれより少ないと硬度が高くなりす
ぎる。The weight ratio of each compound to be copolymerized is preferably in the range of 10:90 to 90:10: acrylic acid compound and/or methacrylic acid compound: vinyl acetate (monomer); if the vinyl acetate component is larger than this, polyvinyl acetate Since the number of parts increases, the hardness of the solidified product obtained will not be sufficient. Conversely, if the vinyl acetate component is less than this, the hardness will be too high.
本発明に使用される(c)のゴムラテックスとしては、
スチレン−ブタジェン共重合体(SBR)、ビニルピリ
ジンSBR、カルボキシ変性SBR、アクリロニトリル
・ブタジェン共重合体(NBI?)、天然ゴム等のラテ
ックスがある。SBRラテックスとしては、SBRラテ
ックス及びカルボキシ変性SBRラテックスを単独ある
いは混合して用いるのが望ましい。混合する場合、カル
ボキシ変性SBRラテックスの割合を多くすると、得ら
れるアスファルト系エマルジョンの固化後の引張り強度
と弾性が高くなるので、用途に応じて適宜配合比を変え
ればよい。The rubber latex (c) used in the present invention includes:
There are latexes such as styrene-butadiene copolymer (SBR), vinylpyridine SBR, carboxy-modified SBR, acrylonitrile-butadiene copolymer (NBI?), and natural rubber. As the SBR latex, it is desirable to use SBR latex and carboxy-modified SBR latex alone or in combination. When mixing, increasing the proportion of carboxy-modified SBR latex increases the tensile strength and elasticity of the resulting asphalt emulsion after solidification, so the blending ratio may be changed as appropriate depending on the application.
(b)の共重合体のアニオン性エマルジョンと、(c)
のゴムラテックスとの混合比は、(b):(c) −1
:10G〜240:10G (固形分換算重量比、以
下同じ)が適当であり、lO:100〜120:100
がより好ましい。(b) an anionic emulsion of the copolymer; and (c)
The mixing ratio with rubber latex is (b):(c) -1
:10G to 240:10G (solid content weight ratio, same below) is appropriate, and lO:100 to 120:100
is more preferable.
また、(a)のアスファルト乳剤等と(b)のアニオン
性エマルジョンとの混合比は(a):(b ) −99
:1〜50:50、(a)のアスファルト乳剤等と(b
)のアニオン性エマルジョンと(c)のゴムラテックス
との混合比は(a): (b)+(c)−99:1〜
70:30の固形分重量比とする。゛(b)成分単独あ
るいは(b)成分と(c)成分の合計量がこれより多い
と得られるアスファルト系エマルジョンの固化速度が速
くなり過ぎて亀裂部分への注入が不可能になり、またこ
れより少いと同化時間が長くかかり過ぎて(1週間以上
)好ましくな・い。Also, the mixing ratio of (a) asphalt emulsion etc. and (b) anionic emulsion is (a):(b) -99
:1 to 50:50, asphalt emulsion etc. of (a) and (b)
The mixing ratio of the anionic emulsion in ) and the rubber latex in (c) is (a): (b) + (c) -99:1 ~
The solids weight ratio is 70:30.゛If the amount of component (b) alone or the total amount of components (b) and (c) is greater than this, the solidification rate of the resulting asphalt-based emulsion will become too fast, making it impossible to inject into cracks. If the amount is less, the assimilation time will take too long (more than a week), which is undesirable.
なお本発明においては、さらに耐候性、耐寒性、柔軟性
の向上をはかるために、老化防止剤や可塑剤を、得られ
るアスファルト系エマルジョンのゴム成分の5重量%以
下の割合で添加することができる。可塑剤としてはポリ
ブテン−1やフタル酸エステル系化合物(フタル酸ジオ
クチルヘキシル、フタル酸ジメチル等)、脂肪族二塩基
酸エステル系化合物(コハク酸ジイソデシル等)、グリ
コールエステル系化合物(ジエチレングリコールジベン
ゾエート等)、脂肪酸エステル系化合物(オレイン酸ブ
チル等、)リン酸エステル系化合物(トリクレジル等)
等がある。また、硬化促進剤、増量剤、あるいは増粘剤
として、アルミナやマグネシア、酸化鉄等の金属酸化物
、金属粉末、石粉(炭酸カルシウム粉末)、砕石粉、砂
利、木粉(もみがら、おがくず等)、セメント、クレー
等の充填剤を、得られるアスファルト系エマルジョンの
固形分の10%以下の割合で添加することができる。In addition, in the present invention, in order to further improve weather resistance, cold resistance, and flexibility, anti-aging agents and plasticizers may be added at a rate of 5% by weight or less of the rubber component of the asphalt emulsion obtained. can. Plasticizers include polybutene-1, phthalate ester compounds (dioctylhexyl phthalate, dimethyl phthalate, etc.), aliphatic dibasic acid ester compounds (diisodecyl succinate, etc.), and glycol ester compounds (diethylene glycol dibenzoate, etc.). , fatty acid ester compounds (butyl oleate, etc.), phosphate ester compounds (tricresyl, etc.)
etc. In addition, as hardening accelerators, extenders, or thickeners, alumina, magnesia, metal oxides such as iron oxide, metal powders, stone powder (calcium carbonate powder), crushed stone powder, gravel, wood powder (rice husks, sawdust, etc.) ), cement, clay, and other fillers can be added at a rate of 10% or less of the solid content of the resulting asphalt emulsion.
本発明のアスファルト系エマルジョンを道路の亀裂部等
に充填する場合には、充填する直前か数日前に上記の各
成分を混合したものを、ノズルやホース等によって亀裂
等に注入すればよい。When filling cracks in roads with the asphalt emulsion of the present invention, a mixture of the above-mentioned components may be injected into the cracks using a nozzle, hose, etc. just before filling or several days before filling.
(作用)
本発明のアスファルト系エマルジョンは、アスファルト
乳剤等に上記共重合体エマルジョンやゴムラテックス等
を添加したことにより、アスファルト系エマルジョンの
固化時間が適当に調整され、路面等の亀裂の先端部にま
で確実に充填することができ、かつ硬化も適当な時間内
に行なわせることができる。さらに共重合体エマルジョ
ンやゴムラテックス等の存在により固化物がゴム弾性や
耐寒性等の優れた特性を発揮する。(Function) The asphalt emulsion of the present invention has the above-mentioned copolymer emulsion, rubber latex, etc. added to the asphalt emulsion, etc., so that the solidification time of the asphalt emulsion is appropriately adjusted, and the solidification time of the asphalt emulsion is adjusted appropriately, so that the asphalt emulsion can be applied to the tips of cracks on the road surface, etc. It is possible to reliably fill up to 100%, and also to cure within an appropriate amount of time. Furthermore, due to the presence of copolymer emulsion, rubber latex, etc., the solidified product exhibits excellent properties such as rubber elasticity and cold resistance.
またさらにアニオン性に調整することにより°エマルジ
ョンの安定性が向上し、長期に亘って安定な状態を維持
することができる。Further, by adjusting the emulsion to be anionic, the stability of the emulsion can be improved and a stable state can be maintained for a long period of time.
(実施例) 以下、本発明の実施例について説明する。(Example) Examples of the present invention will be described below.
実施例1〜9
次表に示す配合で各成分を混合してアスファルト系エマ
ルジョンを調製した。なお、使用した各成分は次のよう
にして調整したものである。Examples 1 to 9 Asphalt emulsions were prepared by mixing each component in the formulation shown in the following table. In addition, each component used was adjusted as follows.
アスファルト乳剤ニアスフアルドを加熱溶融し、これを
アニオン系界面活性剤を溶解した水中に、アスファルト
:水が50:50となるように注下して撹拌し分散させ
たもの。Asphalt emulsion Niasphald is heated and melted, poured into water in which an anionic surfactant has been dissolved, at a ratio of asphalt:water of 50:50, and stirred and dispersed.
ゴム・アスファルト乳剤:ゴムラテックス100部(固
形分50%)°に加熱溶出したアスファルト100部を
注下し、さらにアニオン系界面活性剤と分散安定剤とを
添加して撹拌し分散させたもの。Rubber/asphalt emulsion: 100 parts of heat-eluted asphalt is poured into 100 parts of rubber latex (solid content: 50%), and an anionic surfactant and a dispersion stabilizer are added to the mixture, followed by stirring and dispersion.
共重合体エマルジョン*1:メタクリル酸メチルモノマ
ーを10部と酢酸ビニルモノマーの10部とを20部の
水に溶解し、界面活性剤を4部、重合触媒として過硫酸
アンモニウムを1部添加し、85〜90℃で8時間撹拌
し、重合した後、アンモニア水を注下してpl+8.5
に調整したもの。Copolymer emulsion *1: Dissolve 10 parts of methyl methacrylate monomer and 10 parts of vinyl acetate monomer in 20 parts of water, add 4 parts of surfactant and 1 part of ammonium persulfate as a polymerization catalyst, After stirring at ~90°C for 8 hours and polymerizing, aqueous ammonia was poured to bring the pl+8.5
adjusted to.
共重合体エマルジョン*2ニアクリル酸メチルモノマー
を10部と酢酸ビニルモノマーの10部とを20部の水
に溶解し、界面活性剤を4部、重合触媒として過硫酸ア
ンモニウムを1部添加し、85〜90℃で0時間撹拌し
、重合した後、アンモニア水を注下してpl+8.5に
調整したもの。Copolymer emulsion *2 10 parts of methyl acrylate monomer and 10 parts of vinyl acetate monomer are dissolved in 20 parts of water, 4 parts of surfactant and 1 part of ammonium persulfate as a polymerization catalyst are added, and 85~ After stirring at 90°C for 0 hours and polymerizing, aqueous ammonia was added to adjust the PL to +8.5.
SBRラテックス:固形分50%、ガラス転移点−69
℃。SBR latex: solid content 50%, glass transition point -69
℃.
NBRラテックス:固形分50%、ガラス転移点−55
℃。NBR latex: solid content 50%, glass transition point -55
℃.
メタクリル酸メチルエマルジョン:メタクリル酸メチル
モノマーの10部を10部の水に溶解し、界面活性剤を
2部、重合触媒として過硫酸アンモニウムを0.5部添
加し、85〜90℃で6時間撹拌し、重合した後、アン
モニア水を注下してpH8,5に調整したもの。Methyl methacrylate emulsion: Dissolve 10 parts of methyl methacrylate monomer in 10 parts of water, add 2 parts of surfactant and 0.5 part of ammonium persulfate as a polymerization catalyst, and stir at 85-90°C for 6 hours. , After polymerization, the pH was adjusted to 8.5 by pouring aqueous ammonia.
また比較のために、表中比較例に示すように、本発明の
組成から外れた割合で各成分を混合し、アスファルト系
エマルジョンを調製した。For comparison, as shown in Comparative Example in the table, asphalt emulsions were prepared by mixing each component in a ratio different from the composition of the present invention.
次いで実施例および比較例でそれぞれ得られたアスファ
・ルト系エマルジョンに対して、以下の方法で各種の試
験を行った。Next, various tests were conducted on the asphalt emulsions obtained in the Examples and Comparative Examples using the following methods.
針入度および軟化点: JIS K 22085.13
1:準じて測定した。Penetration and softening point: JIS K 22085.13
1: Measured in the same manner.
ガラス転移点:示差走査熱量計を用いて測定した。Glass transition point: Measured using a differential scanning calorimeter.
固化時間:容積200ccのポリ容器内に試料20gを
とり、空気中(約23℃)に放置したときの固化に要す
る時間を測定した。Solidification time: 20g of a sample was placed in a plastic container with a volume of 200cc, and the time required for solidification when left in the air (about 23°C) was measured.
耐候性:直径15o+sの円板上に試料を3a+mの厚
さに設け、これを45@の角度に立てかけた状態で屋外
暴露し、クラックの有無を調べた。Weather resistance: A sample with a thickness of 3a+m was placed on a disk with a diameter of 15o+s, and exposed outdoors while leaning at an angle of 45@, and the presence or absence of cracks was examined.
これらの測定結果を次表の下欄に示す。The results of these measurements are shown in the lower column of the table below.
(以下余白)
同表に示したように本発明のアスファルト系エマルジョ
ンは、適当な固化時間を有し、各成分の混合比を変える
ことによって固化時間を容易に調整することができる。(The following is a blank space) As shown in the same table, the asphalt emulsion of the present invention has an appropriate solidification time, and the solidification time can be easily adjusted by changing the mixing ratio of each component.
さらにガラス転移点と軟化点との差が大きいので、幅広
い温度範囲に適用することができ、かつ耐候性にも優れ
ている。Furthermore, since the difference between the glass transition point and the softening point is large, it can be applied over a wide temperature range and has excellent weather resistance.
[発明の効果]
本発明のアスファルト系エマルジョンは、前述のように
構成されているので、以下に述べるような効果を発揮す
る。[Effects of the Invention] Since the asphalt emulsion of the present invention is configured as described above, it exhibits the following effects.
(a)成分としてアスファルト乳剤を使用した場合には
、浸透性が良好で作業上も安全であり、またゴム・アス
ファルト乳剤を使用した場合には、これらの効果に加え
て固化物の軟化点、ゴム弾性、耐候性がさらに向上し、
夏期にも充分に特性を発揮する。またこれらの主剤にア
ニオン性のアクリル酸化合物および/またはメタクリル
酸化合物と酢酸ビニルとの共重合体エマルシヨンが使用
されているので、乾燥固化に要する時間が大幅に短縮さ
れ、かつ耐寒性が向上する。When an asphalt emulsion is used as component (a), it has good permeability and is safe to work with, and when a rubber asphalt emulsion is used, in addition to these effects, the softening point of the solidified product, Rubber elasticity and weather resistance are further improved,
It fully demonstrates its characteristics even in the summer. In addition, since a copolymer emulsion of an anionic acrylic acid compound and/or methacrylic acid compound and vinyl acetate is used as the main ingredient, the time required for drying and solidification is significantly shortened and cold resistance is improved. .
さらにこれらの硬化剤とともにゴムラテックスを併用す
ると、エマルジョン中のゴム成分の割合が多くなるので
、弾力性などの機械的特性がさらに向上し、外力が加わ
ってもクラックを生じにくい。Furthermore, when rubber latex is used together with these curing agents, the proportion of rubber components in the emulsion increases, so mechanical properties such as elasticity are further improved, and cracks are less likely to occur even when external forces are applied.
Claims (2)
スファルト乳剤と、(b)アクリル酸化合物および/ま
たはメタクリル酸化合物と酢酸ビニルとを酸性触媒の存
在下で重合させ、アルカリでpHを7より大とした共重
合体のアニオン性エマルジョンとを、(a):(b)=
99:1〜50:50の固形分重量比で混合してなるこ
とを特徴とするアスファルト系エマルジョン。(1) (a) Asphalt emulsion and/or rubber/asphalt emulsion, (b) acrylic acid compound and/or methacrylic acid compound, and vinyl acetate are polymerized in the presence of an acidic catalyst, and the pH is increased to higher than 7 with an alkali. (a):(b)=
An asphalt emulsion characterized by being mixed at a solid content weight ratio of 99:1 to 50:50.
スファルト乳剤と、(b)アクリル酸化合物および/ま
たはメタクリル酸化合物と酢酸ビニルとを酸性触媒の存
在下で重合させ、アルカリでpHを7より大とした共重
合体のアニオン性エマルジョンと、(c)ゴムラテック
スとを、(a):(b)+(c)=99:1〜70:3
0の固形分重量比で混合してなることを特徴とするアス
ファルト系エマルジョン。(2) Polymerize (a) an asphalt emulsion and/or a rubber/asphalt emulsion, (b) an acrylic acid compound and/or a methacrylic acid compound, and vinyl acetate in the presence of an acidic catalyst, and then raise the pH to more than 7 with an alkali. An anionic emulsion of the copolymer and (c) rubber latex, (a):(b)+(c)=99:1 to 70:3
An asphalt emulsion characterized by being mixed at a solid content weight ratio of 0.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16635489A JPH0331340A (en) | 1989-06-27 | 1989-06-27 | Asphalt emulsion |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16635489A JPH0331340A (en) | 1989-06-27 | 1989-06-27 | Asphalt emulsion |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0331340A true JPH0331340A (en) | 1991-02-12 |
Family
ID=15829829
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16635489A Pending JPH0331340A (en) | 1989-06-27 | 1989-06-27 | Asphalt emulsion |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0331340A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003082986A1 (en) * | 2000-10-04 | 2003-10-09 | Nippon Shokubai Co., Ltd. | Asphalt modifying material having specific composition, modified asphalt mixture and method of pavement using the same, and composition |
-
1989
- 1989-06-27 JP JP16635489A patent/JPH0331340A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003082986A1 (en) * | 2000-10-04 | 2003-10-09 | Nippon Shokubai Co., Ltd. | Asphalt modifying material having specific composition, modified asphalt mixture and method of pavement using the same, and composition |
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