NO311576B1 - Bitumen/polymerblandinger med forbedret stabilitet og anvendelse derav for fremstilling av overflatebelegg - Google Patents
Bitumen/polymerblandinger med forbedret stabilitet og anvendelse derav for fremstilling av overflatebelegg Download PDFInfo
- Publication number
- NO311576B1 NO311576B1 NO19980084A NO980084A NO311576B1 NO 311576 B1 NO311576 B1 NO 311576B1 NO 19980084 A NO19980084 A NO 19980084A NO 980084 A NO980084 A NO 980084A NO 311576 B1 NO311576 B1 NO 311576B1
- Authority
- NO
- Norway
- Prior art keywords
- bitumen
- ethylene
- weight
- polymer
- copolymers
- Prior art date
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- 239000010426 asphalt Substances 0.000 title claims abstract description 132
- 238000000576 coating method Methods 0.000 title claims abstract description 5
- 229920002959 polymer blend Polymers 0.000 title claims description 48
- 238000002360 preparation method Methods 0.000 title description 5
- 239000000203 mixture Substances 0.000 claims abstract description 80
- 229920000642 polymer Polymers 0.000 claims abstract description 69
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims abstract description 25
- 239000004593 Epoxy Substances 0.000 claims abstract description 24
- 229920005596 polymer binder Polymers 0.000 claims abstract description 8
- 239000002491 polymer binding agent Substances 0.000 claims abstract description 8
- 229920001971 elastomer Polymers 0.000 claims abstract description 5
- 239000000806 elastomer Substances 0.000 claims abstract description 5
- 229920001577 copolymer Polymers 0.000 claims description 71
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 68
- 239000005977 Ethylene Substances 0.000 claims description 65
- 239000000178 monomer Substances 0.000 claims description 34
- -1 C12 diene Chemical class 0.000 claims description 31
- 230000001788 irregular Effects 0.000 claims description 18
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 17
- 239000000654 additive Substances 0.000 claims description 17
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 claims description 16
- 125000005250 alkyl acrylate group Chemical group 0.000 claims description 14
- 229920001684 low density polyethylene Polymers 0.000 claims description 14
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 14
- 229920001897 terpolymer Polymers 0.000 claims description 14
- 239000004215 Carbon black (E152) Substances 0.000 claims description 12
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims description 12
- 229930195733 hydrocarbon Natural products 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 claims description 12
- BAPJBEWLBFYGME-UHFFFAOYSA-N acrylic acid methyl ester Natural products COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 11
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 11
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 11
- 150000002430 hydrocarbons Chemical class 0.000 claims description 11
- 239000004743 Polypropylene Substances 0.000 claims description 10
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 10
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 10
- 229920000636 poly(norbornene) polymer Polymers 0.000 claims description 10
- 229920001155 polypropylene Polymers 0.000 claims description 10
- 239000010413 mother solution Substances 0.000 claims description 9
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical group COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Chemical group OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 8
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical group CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 8
- 150000008064 anhydrides Chemical group 0.000 claims description 8
- 230000004907 flux Effects 0.000 claims description 8
- 239000004702 low-density polyethylene Substances 0.000 claims description 8
- 239000011976 maleic acid Substances 0.000 claims description 8
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid group Chemical group C(\C=C/C(=O)O)(=O)O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 8
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 8
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 150000001993 dienes Chemical class 0.000 claims description 7
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 7
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 7
- 229920000768 polyamine Polymers 0.000 claims description 6
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 6
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 6
- 239000004698 Polyethylene Substances 0.000 claims description 5
- 229920002367 Polyisobutene Polymers 0.000 claims description 5
- 229920005549 butyl rubber Polymers 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 5
- 125000003700 epoxy group Chemical group 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 229920002857 polybutadiene Polymers 0.000 claims description 5
- 229920000573 polyethylene Polymers 0.000 claims description 5
- 229920001195 polyisoprene Polymers 0.000 claims description 5
- 230000000996 additive effect Effects 0.000 claims description 4
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 claims description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
- 229920001519 homopolymer Polymers 0.000 claims description 4
- 229920001083 polybutene Polymers 0.000 claims description 4
- 229920005862 polyol Polymers 0.000 claims description 4
- 150000003077 polyols Chemical class 0.000 claims description 4
- 229920002725 thermoplastic elastomer Polymers 0.000 claims description 4
- 239000005062 Polybutadiene Substances 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- 238000007865 diluting Methods 0.000 claims description 3
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims description 3
- 239000000155 melt Substances 0.000 claims description 3
- 229920001084 poly(chloroprene) Polymers 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 2
- JJRUAPNVLBABCN-UHFFFAOYSA-N 2-(ethenoxymethyl)oxirane Chemical compound C=COCC1CO1 JJRUAPNVLBABCN-UHFFFAOYSA-N 0.000 claims description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Natural products CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
- 229920000800 acrylic rubber Polymers 0.000 claims description 2
- 150000001298 alcohols Chemical class 0.000 claims description 2
- 150000001336 alkenes Chemical class 0.000 claims description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N alpha-Methyl-n-butyl acrylate Natural products CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims description 2
- 239000011230 binding agent Substances 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 239000000839 emulsion Substances 0.000 claims description 2
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 claims description 2
- GFJVXXWOPWLRNU-UHFFFAOYSA-N ethenyl formate Chemical compound C=COC=O GFJVXXWOPWLRNU-UHFFFAOYSA-N 0.000 claims description 2
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 claims description 2
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 229920001903 high density polyethylene Polymers 0.000 claims description 2
- 239000004700 high-density polyethylene Substances 0.000 claims description 2
- 150000002734 metacrylic acid derivatives Chemical class 0.000 claims description 2
- 150000002739 metals Chemical class 0.000 claims description 2
- 230000000737 periodic effect Effects 0.000 claims description 2
- 150000003141 primary amines Chemical class 0.000 claims description 2
- 150000003335 secondary amines Chemical class 0.000 claims description 2
- 239000000758 substrate Substances 0.000 claims description 2
- 239000004711 α-olefin Substances 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 238000010790 dilution Methods 0.000 abstract description 3
- 239000012895 dilution Substances 0.000 abstract description 3
- 229920000034 Plastomer Polymers 0.000 abstract description 2
- 239000000463 material Substances 0.000 abstract 1
- 238000003756 stirring Methods 0.000 description 10
- 239000003208 petroleum Substances 0.000 description 6
- 238000003860 storage Methods 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 230000007903 penetration ability Effects 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- PWGJDPKCLMLPJW-UHFFFAOYSA-N 1,8-diaminooctane Chemical compound NCCCCCCCCN PWGJDPKCLMLPJW-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 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
- 125000003277 amino group Chemical group 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 150000004984 aromatic diamines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- GHWVXCQZPNWFRO-UHFFFAOYSA-N butane-2,3-diamine Chemical compound CC(N)C(C)N GHWVXCQZPNWFRO-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- VHQNTEJDZCFQHP-UHFFFAOYSA-N cyclododecane-1,1-diamine Chemical compound NC1(N)CCCCCCCCCCC1 VHQNTEJDZCFQHP-UHFFFAOYSA-N 0.000 description 1
- YMHQVDAATAEZLO-UHFFFAOYSA-N cyclohexane-1,1-diamine Chemical compound NC1(N)CCCCC1 YMHQVDAATAEZLO-UHFFFAOYSA-N 0.000 description 1
- XHMWGEWUBYMZDB-UHFFFAOYSA-N cyclooctane-1,1-diamine Chemical compound NC1(N)CCCCCCC1 XHMWGEWUBYMZDB-UHFFFAOYSA-N 0.000 description 1
- OWEZJUPKTBEISC-UHFFFAOYSA-N decane-1,1-diamine Chemical compound CCCCCCCCCC(N)N OWEZJUPKTBEISC-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- JMLPVHXESHXUSV-UHFFFAOYSA-N dodecane-1,1-diamine Chemical compound CCCCCCCCCCCC(N)N JMLPVHXESHXUSV-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 150000004675 formic acid derivatives Chemical class 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- GKQPCPXONLDCMU-CCEZHUSRSA-N lacidipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C GKQPCPXONLDCMU-CCEZHUSRSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000004704 methoxides Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- NTNWKDHZTDQSST-UHFFFAOYSA-N naphthalene-1,2-diamine Chemical compound C1=CC=CC2=C(N)C(N)=CC=C21 NTNWKDHZTDQSST-UHFFFAOYSA-N 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- ZNZJJSYHZBXQSM-UHFFFAOYSA-N propane-2,2-diamine Chemical compound CC(C)(N)N ZNZJJSYHZBXQSM-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 229940034610 toothpaste Drugs 0.000 description 1
- 239000000606 toothpaste Substances 0.000 description 1
- 229960001124 trientine Drugs 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L95/00—Compositions of bituminous materials, e.g. asphalt, tar, pitch
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/16—Elastomeric ethene-propene or ethene-propene-diene copolymers, e.g. EPR and EPDM rubbers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/10—Homopolymers or copolymers of methacrylic acid esters
- C08L33/12—Homopolymers or copolymers of methyl methacrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D195/00—Coating compositions based on bituminous materials, e.g. asphalt, tar, pitch
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/04—Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/04—Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
- C08L2666/08—Homopolymers or copolymers according to C08L7/00 - C08L21/00; Derivatives thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Structural Engineering (AREA)
- Civil Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Road Paving Structures (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9605827A FR2748487B1 (fr) | 1996-05-10 | 1996-05-10 | Compositions bitume/polymere a stabilite amelioree et leur application a la realisation de revetements |
| PCT/FR1997/000811 WO1997043341A1 (fr) | 1996-05-10 | 1997-05-06 | Compositions bitume/polymere a stabilite amelioree et leur application a la realisation de revetements |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO980084D0 NO980084D0 (no) | 1998-01-08 |
| NO980084L NO980084L (no) | 1998-03-02 |
| NO311576B1 true NO311576B1 (no) | 2001-12-10 |
Family
ID=9492008
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19980084A NO311576B1 (no) | 1996-05-10 | 1998-01-08 | Bitumen/polymerblandinger med forbedret stabilitet og anvendelse derav for fremstilling av overflatebelegg |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US6020404A (ko) |
| EP (1) | EP0837909B1 (ko) |
| JP (1) | JPH11509889A (ko) |
| KR (1) | KR19990028873A (ko) |
| CN (1) | CN1152090C (ko) |
| AT (1) | ATE259397T1 (ko) |
| AU (1) | AU2902597A (ko) |
| BR (1) | BR9702204A (ko) |
| CA (1) | CA2224415C (ko) |
| DE (1) | DE69727528T2 (ko) |
| ES (1) | ES2216148T3 (ko) |
| FR (1) | FR2748487B1 (ko) |
| ID (1) | ID18235A (ko) |
| MX (1) | MX9800117A (ko) |
| MY (1) | MY129081A (ko) |
| NO (1) | NO311576B1 (ko) |
| WO (1) | WO1997043341A1 (ko) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69628553T2 (de) | 1995-03-13 | 2004-04-29 | Mathy Construction Co., Onalaska | Mit säure umgesetzte, polymermodifizierte asphaltzusammensetzungen und deren herstellung |
| FR2748488B1 (fr) * | 1996-05-10 | 1998-07-10 | Elf Antar France | Procede de preparation de compositions bitume/polymere a tres faible susceptibilite thermique et application des compositions obtenues a la production de liants bitume/polymere pour revetements |
| JPH10120839A (ja) * | 1996-10-15 | 1998-05-12 | Sumitomo Chem Co Ltd | アスファルト改質材及び該改質材を含むアスファルト組成物 |
| JPH10120843A (ja) * | 1997-06-12 | 1998-05-12 | Sumitomo Chem Co Ltd | アスファルト改質材及び該改質材を含むアスファルト組成物 |
| FR2795418B1 (fr) * | 1999-06-22 | 2001-09-28 | Elf Antar France | Procede de preparation de compositions bitume/polymere reticulees et/ou fonctionnalisees a tres faible susceptibilite thermique et application des compositions obtenues a la realisation de revetements |
| US7081492B1 (en) | 2000-05-16 | 2006-07-25 | Dennis Krivohlavek | Ambient temperature anhydrous liquid cross-linking agent |
| US20030187104A1 (en) * | 2002-04-01 | 2003-10-02 | Guilbault Lawrence James | Polymer-modified asphalt |
| FR2849047B1 (fr) * | 2002-12-20 | 2005-12-02 | Totalfinaelf France | Procede de preparation de compositions bitume/polymere a resistance aux solvants petroliers amelioree, compositions ainsi obtenues et leur utilisation comme liant bitumineux |
| FR2849048B1 (fr) * | 2002-12-23 | 2005-11-04 | Totalfinaelf France | Procede de preparation de compositions bitume/polymere epoxyde reticule, composition ainsi obtenues et leur utilisation |
| FR2878856B1 (fr) * | 2004-12-03 | 2007-04-06 | Smac Acieroid Sa | Enrobe bitumineux, procede de preparation, et applications de cet enrobe |
| BRPI0613289A2 (pt) * | 2005-06-23 | 2010-12-28 | Du Pont | composição, processo, uso de uma composição e pavimentação de rodovia ou folha de telhado |
| FR2918066B1 (fr) | 2007-06-26 | 2010-11-19 | Total France | Liant concentre non gelifiable et pompable pour bitume/polymere |
| FR2919298B1 (fr) | 2007-07-24 | 2012-06-08 | Total France | Composition bitume/polymere a reticulation thermoreversible. |
| FR2919294B1 (fr) | 2007-07-24 | 2012-11-16 | Total France | Polymere greffe et composition de bitume a reticulation thermoreversible comprenant ledit polymere greffe. |
| US8076399B2 (en) | 2007-12-07 | 2011-12-13 | Shell Oil Company | Binder composition and asphalt mixture |
| FR2929616B1 (fr) | 2008-04-08 | 2011-09-09 | Total France | Procede de reticulation de compositions bitume/polymere presentant des emissions reduites d'hydrogene sulfure |
| US9896582B2 (en) | 2009-03-08 | 2018-02-20 | Lehigh Technologies, Inc. | Micronized asphalt modifiers, methods of modifying asphalt, asphalt compositions and methods of making |
| US9617424B2 (en) * | 2009-03-08 | 2017-04-11 | Lehigh Technologies, Inc. | Polyolefin asphalt modifiers, methods of modifying asphalt, asphalt compositions and methods of making |
| US9884965B2 (en) | 2009-03-08 | 2018-02-06 | Lehigh Tehnologies, Inc. | Functional group asphalt modifiers, methods of modifying asphalt, asphalt compositions and methods of making |
| US8541523B2 (en) * | 2010-04-05 | 2013-09-24 | Promerus, Llc | Norbornene-type polymers, compositions thereof and lithographic process using such compositions |
| CN102086349B (zh) * | 2010-12-10 | 2012-10-03 | 上海台安工程实业有限公司 | 一种具双重特性的非固化防水涂胶 |
| CN102399493A (zh) * | 2011-10-27 | 2012-04-04 | 北京东方雨虹防水技术股份有限公司 | 蠕变型热熔橡胶沥青防水涂料 |
| FR2984342B1 (fr) | 2011-12-20 | 2014-01-03 | Total Raffinage Marketing | Procede de production d'une composition bitume/polymere reticulee avec reduction des emissions de h2s |
| CN102604297B (zh) | 2012-03-09 | 2013-11-13 | 湖北省高速公路实业开发有限公司 | 一种沥青路面用缓释型防冰材料及其制备方法 |
| CN103030314B (zh) * | 2012-12-31 | 2015-01-07 | 哈尔滨工业大学 | 一种沥青混合料缓释络合盐填料的制备方法 |
| FR3005058B1 (fr) | 2013-04-25 | 2017-09-08 | Arkema France | Composition de pre-melange pour bitumes |
| CN103525303A (zh) * | 2013-09-27 | 2014-01-22 | 吴润秀 | 聚烯烃涂料 |
| CN104987607A (zh) * | 2015-06-30 | 2015-10-21 | 南阳理工学院 | 一种防腐防水材料 |
| FR3041355B1 (fr) | 2015-09-18 | 2017-09-01 | Total Marketing Services | Composition bitume / polymere presentant des proprietes mecaniques ameliorees |
| WO2017116831A1 (en) * | 2015-12-29 | 2017-07-06 | E. I. Du Pont De Nemours And Company | Modified asphalt using epoxide-containing polymers |
| CN110093836A (zh) * | 2018-01-27 | 2019-08-06 | 深圳善跑体育产业集团有限公司 | 塑胶跑道及施工工艺 |
| FR3080856B1 (fr) | 2018-05-02 | 2020-07-10 | Total Marketing Services | Composition bitume/polymere presentant des proprietes mecaniques ameliorees |
| FR3099486B1 (fr) | 2019-07-31 | 2023-04-28 | Total Marketing Services | Composition bitume/polymère fluxée et son procédé de préparation |
| CN113683959B (zh) * | 2021-10-27 | 2022-02-18 | 科顺防水科技股份有限公司 | 双组份橡胶沥青防水涂料组合物及应用该双组份橡胶沥青防水涂料组合物的结构 |
| JP2023170479A (ja) * | 2022-05-19 | 2023-12-01 | 住友化学株式会社 | アスファルト組成物及びアスファルト舗装材組成物 |
| CN116814160B (zh) * | 2023-05-26 | 2023-12-19 | 佛山市科顺建筑材料有限公司 | 一种反应改性沥青防水卷材涂盖料组合物、防水卷材涂盖料及其制备方法与应用 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1511604A (fr) * | 1966-12-19 | 1968-02-02 | Produits élasto-plastiques et leur application | |
| CA1282513C (en) * | 1986-03-04 | 1991-04-02 | Raymond T. Woodhams | Bitumen - polyolefin compositions |
| US4818367A (en) * | 1986-04-14 | 1989-04-04 | J. H. Diamond Company | Asphalt, copolymer and elastomer composition |
| EP0384254A3 (en) * | 1989-02-21 | 1992-04-01 | BASF Aktiengesellschaft | Latex compounds for asphalt modifications |
| EP0507838A4 (en) * | 1989-12-29 | 1993-03-17 | Chevron Research Company | Polymer and asphalt reaction process and polymer-linked-asphalt product |
| DE4128640A1 (de) * | 1991-08-29 | 1993-03-04 | Roehm Gmbh | Alkyl(meth)acrylat-maleinsaeureanhydrid copolymer-modifiziertes bitumen |
| JPH06116333A (ja) * | 1992-10-02 | 1994-04-26 | Elf Atochem Japan Kk | 改良された舗装用アスファルト組成物 |
| US5331028A (en) * | 1993-06-30 | 1994-07-19 | Chevron Research And Technology Company, A Division Of Chevron U.S.A. Inc. | Polymer-modified asphalt composition and process for the preparation thereof |
| FR2718747B1 (fr) * | 1994-04-18 | 1996-06-07 | Elf Antar France | Procédé de préparation de compositions bitume/polymère à caractère multigrade renforcé et application des compositions obtenues à la production de liants bitume/polymère pour revêtements. |
| EP0718373A1 (en) * | 1994-12-20 | 1996-06-26 | Bridgestone/Firestone, Inc. | Polymer modified asphaltic compounds with improved dispersion and improved products therefrom |
| JPH08199073A (ja) * | 1995-01-30 | 1996-08-06 | Elf Atochem Japan Kk | 改質アスファルト組成物 |
| US5708062A (en) * | 1995-01-30 | 1998-01-13 | Elf Atochem S.A. | Bitumen compositions |
-
1996
- 1996-05-10 FR FR9605827A patent/FR2748487B1/fr not_active Expired - Fee Related
-
1997
- 1997-05-06 KR KR1019980700175A patent/KR19990028873A/ko not_active Application Discontinuation
- 1997-05-06 AU AU29025/97A patent/AU2902597A/en not_active Abandoned
- 1997-05-06 WO PCT/FR1997/000811 patent/WO1997043341A1/fr active IP Right Grant
- 1997-05-06 US US08/983,300 patent/US6020404A/en not_active Expired - Lifetime
- 1997-05-06 MX MX9800117A patent/MX9800117A/es unknown
- 1997-05-06 CA CA002224415A patent/CA2224415C/fr not_active Expired - Lifetime
- 1997-05-06 AT AT97923148T patent/ATE259397T1/de not_active IP Right Cessation
- 1997-05-06 DE DE69727528T patent/DE69727528T2/de not_active Expired - Lifetime
- 1997-05-06 JP JP9540577A patent/JPH11509889A/ja active Pending
- 1997-05-06 BR BR9702204A patent/BR9702204A/pt not_active IP Right Cessation
- 1997-05-06 CN CNB971906947A patent/CN1152090C/zh not_active Expired - Lifetime
- 1997-05-06 ES ES97923148T patent/ES2216148T3/es not_active Expired - Lifetime
- 1997-05-06 EP EP97923148A patent/EP0837909B1/fr not_active Expired - Lifetime
- 1997-05-09 MY MYPI97002039A patent/MY129081A/en unknown
- 1997-05-12 ID IDP971581A patent/ID18235A/id unknown
-
1998
- 1998-01-08 NO NO19980084A patent/NO311576B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| ES2216148T3 (es) | 2004-10-16 |
| KR19990028873A (ko) | 1999-04-15 |
| US6020404A (en) | 2000-02-01 |
| NO980084D0 (no) | 1998-01-08 |
| CA2224415A1 (fr) | 1997-11-20 |
| DE69727528D1 (de) | 2004-03-18 |
| JPH11509889A (ja) | 1999-08-31 |
| NO980084L (no) | 1998-03-02 |
| AU2902597A (en) | 1997-12-05 |
| BR9702204A (pt) | 1999-07-20 |
| EP0837909A1 (fr) | 1998-04-29 |
| DE69727528T2 (de) | 2004-12-23 |
| CA2224415C (fr) | 2006-10-17 |
| CN1152090C (zh) | 2004-06-02 |
| ATE259397T1 (de) | 2004-02-15 |
| CN1195362A (zh) | 1998-10-07 |
| MX9800117A (es) | 1998-04-30 |
| MY129081A (en) | 2007-03-30 |
| ID18235A (id) | 1998-03-19 |
| EP0837909B1 (fr) | 2004-02-11 |
| WO1997043341A1 (fr) | 1997-11-20 |
| FR2748487B1 (fr) | 1998-07-10 |
| FR2748487A1 (fr) | 1997-11-14 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK1K | Patent expired |