NO309944B1 - FremgangsmÕte ved fremstilling av elastomer/bitumenblandinger og anvendelse derav som veibelegg, samt stamoppløsning til fremstilling av elastomer/bitumenblandingene - Google Patents
FremgangsmÕte ved fremstilling av elastomer/bitumenblandinger og anvendelse derav som veibelegg, samt stamoppløsning til fremstilling av elastomer/bitumenblandingene Download PDFInfo
- Publication number
- NO309944B1 NO309944B1 NO972809A NO972809A NO309944B1 NO 309944 B1 NO309944 B1 NO 309944B1 NO 972809 A NO972809 A NO 972809A NO 972809 A NO972809 A NO 972809A NO 309944 B1 NO309944 B1 NO 309944B1
- Authority
- NO
- Norway
- Prior art keywords
- bitumen
- elastomer
- mixture
- functionalizing agent
- radicals
- Prior art date
Links
- 239000010426 asphalt Substances 0.000 title claims abstract description 180
- 229920001971 elastomer Polymers 0.000 title claims abstract description 157
- 239000000806 elastomer Substances 0.000 title claims abstract description 157
- 239000000203 mixture Substances 0.000 title claims abstract description 151
- 238000000034 method Methods 0.000 title claims description 33
- 239000011550 stock solution Substances 0.000 title claims description 18
- 238000002360 preparation method Methods 0.000 title description 15
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 49
- -1 peroxide compound Chemical class 0.000 claims abstract description 41
- 238000003756 stirring Methods 0.000 claims abstract description 19
- 239000011230 binding agent Substances 0.000 claims abstract description 11
- 238000000576 coating method Methods 0.000 claims abstract description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 54
- 239000004215 Carbon black (E152) Substances 0.000 claims description 30
- 229930195733 hydrocarbon Natural products 0.000 claims description 30
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 26
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 22
- 239000007795 chemical reaction product Substances 0.000 claims description 20
- 239000000654 additive Substances 0.000 claims description 19
- 238000004519 manufacturing process Methods 0.000 claims description 18
- 150000001993 dienes Chemical class 0.000 claims description 14
- 229920001577 copolymer Polymers 0.000 claims description 13
- 239000003921 oil Substances 0.000 claims description 13
- 230000004907 flux Effects 0.000 claims description 12
- 150000002430 hydrocarbons Chemical class 0.000 claims description 12
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 11
- 229920000768 polyamine Polymers 0.000 claims description 10
- 239000011541 reaction mixture Substances 0.000 claims description 9
- 229920001400 block copolymer Polymers 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 6
- 230000035699 permeability Effects 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 6
- 230000000996 additive effect Effects 0.000 claims description 5
- 238000010790 dilution Methods 0.000 claims description 5
- 239000012895 dilution Substances 0.000 claims description 5
- 230000001788 irregular Effects 0.000 claims description 5
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 claims description 4
- 239000000047 product Substances 0.000 claims description 4
- 150000001298 alcohols Chemical class 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 239000008240 homogeneous mixture Substances 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 150000002736 metal compounds Chemical class 0.000 claims description 3
- 229920005862 polyol Polymers 0.000 claims description 3
- 150000003077 polyols Chemical class 0.000 claims description 3
- 150000001414 amino alcohols Chemical class 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims description 2
- 239000000839 emulsion Substances 0.000 claims description 2
- 150000002118 epoxides Chemical class 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 238000010348 incorporation Methods 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 150000002739 metals Chemical class 0.000 claims description 2
- 230000000737 periodic effect Effects 0.000 claims description 2
- 150000002978 peroxides Chemical class 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
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 claims 4
- 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 claims 1
- 238000010276 construction Methods 0.000 claims 1
- 150000001733 carboxylic acid esters Chemical class 0.000 abstract description 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 238000007789 sealing Methods 0.000 abstract 1
- QERYCTSHXKAMIS-UHFFFAOYSA-N thiophene-2-carboxylic acid Chemical group OC(=O)C1=CC=CS1 QERYCTSHXKAMIS-UHFFFAOYSA-N 0.000 abstract 1
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 8
- 239000012141 concentrate Substances 0.000 description 7
- YCLSOMLVSHPPFV-UHFFFAOYSA-N 3-(2-carboxyethyldisulfanyl)propanoic acid Chemical compound OC(=O)CCSSCCC(O)=O YCLSOMLVSHPPFV-UHFFFAOYSA-N 0.000 description 6
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 6
- 238000004132 cross linking Methods 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 238000007865 diluting Methods 0.000 description 4
- 150000002019 disulfides Chemical class 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 238000007306 functionalization reaction Methods 0.000 description 4
- 229920000642 polymer Polymers 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
- 206010057040 Temperature intolerance Diseases 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 230000008543 heat sensitivity Effects 0.000 description 3
- DKIDEFUBRARXTE-UHFFFAOYSA-N 3-mercaptopropanoic acid Chemical compound OC(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 238000009938 salting Methods 0.000 description 2
- 238000003860 storage Methods 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
- 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
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- WECIKJKLCDCIMY-UHFFFAOYSA-N 2-chloro-n-(2-cyanoethyl)acetamide Chemical compound ClCC(=O)NCCC#N WECIKJKLCDCIMY-UHFFFAOYSA-N 0.000 description 1
- CFPHMAVQAJGVPV-UHFFFAOYSA-N 2-sulfanylbutanoic acid Chemical compound CCC(S)C(O)=O CFPHMAVQAJGVPV-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
- YYSCJLLOWOUSHH-UHFFFAOYSA-N 4,4'-disulfanyldibutanoic acid Chemical compound OC(=O)CCCSSCCCC(O)=O YYSCJLLOWOUSHH-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
- OXIAMGMNWRAVCO-UHFFFAOYSA-N 6-[(6-carboxy-1-hydroxycyclohexa-2,4-dien-1-yl)disulfanyl]-6-hydroxycyclohexa-2,4-diene-1-carboxylic acid Chemical compound OC(=O)C1C=CC=CC1(O)SSC1(O)C(C(O)=O)C=CC=C1 OXIAMGMNWRAVCO-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
- 229920002943 EPDM rubber Polymers 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 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
- 239000002253 acid Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 150000004984 aromatic diamines Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 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
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical group 0.000 description 1
- 210000004534 cecum Anatomy 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000005336 cracking Methods 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
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000004821 distillation 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
- 125000004185 ester group Chemical group 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 150000004675 formic acid derivatives Chemical class 0.000 description 1
- 238000001879 gelation Methods 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
- 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 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000001939 inductive effect Effects 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
- 239000011707 mineral 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
- 239000010742 number 1 fuel oil Substances 0.000 description 1
- OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 1
- 229920000636 poly(norbornene) polymer Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 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
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- ACTRVOBWPAIOHC-UHFFFAOYSA-N succimer Chemical compound OC(=O)C(S)C(S)C(O)=O ACTRVOBWPAIOHC-UHFFFAOYSA-N 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
- 229920001897 terpolymer Polymers 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- NJRXVEJTAYWCQJ-UHFFFAOYSA-N thiomalic acid Chemical compound OC(=O)CC(S)C(O)=O NJRXVEJTAYWCQJ-UHFFFAOYSA-N 0.000 description 1
- 229920000428 triblock copolymer Polymers 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
- 238000005292 vacuum distillation Methods 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10C—WORKING-UP PITCH, ASPHALT, BITUMEN, TAR; PYROLIGNEOUS ACID
- C10C3/00—Working-up pitch, asphalt, bitumen
- C10C3/02—Working-up pitch, asphalt, bitumen by chemical means reaction
- C10C3/026—Working-up pitch, asphalt, bitumen by chemical means reaction with organic compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G81/00—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
- C08G81/02—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers at least one of the polymers being obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C08G81/021—Block or graft polymers containing only sequences of polymers of C08C or C08F
- C08G81/022—Block or graft polymers containing only sequences of polymers of C08C or C08F containing sequences of polymers of conjugated dienes and of polymers of alkenyl aromatic compounds
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Civil Engineering (AREA)
- Structural Engineering (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Sealing Material Composition (AREA)
- Paints Or Removers (AREA)
- Road Paving Structures (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9512276A FR2740140B1 (fr) | 1995-10-19 | 1995-10-19 | Procede de preparation de compositions bitume/elastomere fonctionnalise a large intervalle de plasticite, application des compositions obtenues a la realisation de revetements et solution mere pour cette preparation |
PCT/FR1996/001614 WO1997014754A1 (fr) | 1995-10-19 | 1996-10-16 | Procede de preparation de composition bitume/elastomere, leur application comme revetement routier |
Publications (3)
Publication Number | Publication Date |
---|---|
NO972809D0 NO972809D0 (no) | 1997-06-18 |
NO972809L NO972809L (no) | 1997-08-18 |
NO309944B1 true NO309944B1 (no) | 2001-04-23 |
Family
ID=9483688
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO972809A NO309944B1 (no) | 1995-10-19 | 1997-06-18 | FremgangsmÕte ved fremstilling av elastomer/bitumenblandinger og anvendelse derav som veibelegg, samt stamoppløsning til fremstilling av elastomer/bitumenblandingene |
Country Status (20)
Country | Link |
---|---|
US (1) | US5883162A (de) |
EP (1) | EP0799280B1 (de) |
JP (1) | JP4209944B2 (de) |
KR (1) | KR100521655B1 (de) |
CN (1) | CN1122689C (de) |
AT (1) | ATE234898T1 (de) |
AU (1) | AU7305396A (de) |
BR (1) | BR9607167A (de) |
CA (1) | CA2208587C (de) |
CZ (1) | CZ291716B6 (de) |
DE (1) | DE69626783T2 (de) |
DK (1) | DK0799280T3 (de) |
EE (1) | EE9700130A (de) |
ES (1) | ES2195015T3 (de) |
FR (1) | FR2740140B1 (de) |
MX (1) | MX9704597A (de) |
MY (1) | MY115861A (de) |
NO (1) | NO309944B1 (de) |
PL (1) | PL187259B1 (de) |
WO (1) | WO1997014754A1 (de) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2762322B1 (fr) * | 1997-04-21 | 1999-05-28 | Elf Antar France | Procede de preparation de compositions bitume/polymere, application des compositions obtenues a la production de liants bitume/polymere pour revetements et solution mere de polymere pour l'obtention desdites compositions |
CN1103353C (zh) * | 2000-09-18 | 2003-03-19 | 梁清源 | 沥青共聚烯烃复合材料及其制造方法 |
CN1321156C (zh) * | 2002-04-24 | 2007-06-13 | 旭化成化学株式会社 | 沥青组合物 |
RU2314325C2 (ru) * | 2002-10-11 | 2008-01-10 | Шелл Интернэшнл Рисерч Маатсхаппий Б.В. | Битумная композиция, способ получения и ее применение |
US7517934B2 (en) * | 2003-07-31 | 2009-04-14 | Basf Corporation | Modified anionically polymerized polymers |
ES2261077B1 (es) * | 2005-04-25 | 2007-12-16 | Repsol Ypf, S.A. | Ligante bitunimoso, procedimiento para la aplicacion del mismo y su uso para pavimentacion de carreteras. |
US7820743B2 (en) | 2005-07-21 | 2010-10-26 | Eastern Petroleum Sdn Bhd | Process for preparing bitumen/asphalt bale |
FR2911611B1 (fr) * | 2007-01-23 | 2011-01-07 | Total France | Composition bitumineuse aux proprietes thermoreversibles. |
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. |
FR2924121A1 (fr) | 2007-11-27 | 2009-05-29 | Total France Sa | Composition bitumineuse elastique reticulee de maniere thermoreversible |
FR2929616B1 (fr) | 2008-04-08 | 2011-09-09 | Total France | Procede de reticulation de compositions bitume/polymere presentant des emissions reduites d'hydrogene sulfure |
US20110160355A1 (en) * | 2009-11-06 | 2011-06-30 | Jean-Valery Martin | Asphalt additive with improved performance |
EP2787043B1 (de) * | 2010-04-30 | 2018-03-21 | Total Marketing Services | Einsatz von organogel-bildenden derivaten in bituminösen zusammensetzungen zur verbesserung ihrer widerstandskraft gegen chemische aggressionen |
CN101914365A (zh) * | 2010-09-07 | 2010-12-15 | 阎光生 | 复合反应型路面防水粘接材料 |
FR2984329B1 (fr) | 2011-12-20 | 2014-11-21 | Total Raffinage Marketing | Polymere greffe et composition bitume/polymere a reticulation thermoreversible contenant un tel polymere |
FR2992654B1 (fr) | 2012-07-02 | 2015-08-07 | Total Raffinage Marketing | Compositions bitumineuses additivees aux proprietes thermoreversibles ameliorees |
FR2992653B1 (fr) | 2012-07-02 | 2015-06-19 | Total Raffinage Marketing | Compositions bitumineuses additivees aux proprietes thermoreversibles ameliorees |
WO2016121580A1 (ja) * | 2015-01-30 | 2016-08-04 | 住友化学株式会社 | アスファルト用添加剤 |
KR102063651B1 (ko) * | 2016-03-28 | 2020-01-08 | 주식회사 엘지화학 | 아연 페라이트 촉매의 제조방법 |
CN114479365B (zh) * | 2020-10-27 | 2023-01-10 | 中国石油化工股份有限公司 | 一种抗脱落剂及其制法和应用 |
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DE2513514A1 (de) * | 1974-03-28 | 1975-10-02 | Shell Int Research | Modifiziertes bitumen und modifizierte (misch)-polymerisate enthaltendes mischmaterial und seine verwendung zur herstellung von massen, in denen das bitumen chemisch an das (die) (misch) polymerisat(e) gebunden ist |
GB1508420A (en) * | 1974-03-28 | 1978-04-26 | Shell Int Research | Compositions comprising bitumens and(co)polymers and products comprising bitumens chemically coupled with(co)polymers and their preparation |
US4126482A (en) * | 1975-01-30 | 1978-11-21 | Societe Nationale Des Petroles D'aquitaine | Thiol polyesters |
FR2528439B1 (fr) * | 1982-06-10 | 1985-11-22 | Elf France | Procede de preparation de compositions bitume-polymere, application de ces compositions a la realisation de revetements, et solution mere de polymere utilisable pour l'obtention desdites compositions |
FR2636340B1 (fr) * | 1988-09-09 | 1992-04-17 | Elf France | Procede de preparation de compositions bitume-polymere, application des compositions obtenues a la realisation de revetements et solution mere de polymere utilisable pour l'obtention desdites compositions |
FR2705681A1 (fr) * | 1992-03-03 | 1994-12-02 | Elf Antar France | Procédé de préparation de compositions bitume-polymère, application des compositions obtenues à la réalisation de revêtements et solution mère de polymère pour l'obtention desdites compositions. |
US5719216A (en) * | 1995-05-22 | 1998-02-17 | Shell Oil Company | Preparation process for polymer-modified bitumen |
FR2740138B1 (fr) * | 1995-10-19 | 1997-11-21 | Elf Aquitaine | Elastomere fonctionnalise par des groupements carboxyliques ou esters greffes et son application a la production de compositions bitume/elastomere fonctionnalise utilisables pour la realisation de revetements |
-
1995
- 1995-10-19 FR FR9512276A patent/FR2740140B1/fr not_active Expired - Fee Related
-
1996
- 1996-10-16 MX MX9704597A patent/MX9704597A/es not_active IP Right Cessation
- 1996-10-16 CZ CZ19971927A patent/CZ291716B6/cs not_active IP Right Cessation
- 1996-10-16 WO PCT/FR1996/001614 patent/WO1997014754A1/fr active IP Right Grant
- 1996-10-16 PL PL96320795A patent/PL187259B1/pl not_active IP Right Cessation
- 1996-10-16 ES ES96934920T patent/ES2195015T3/es not_active Expired - Lifetime
- 1996-10-16 KR KR1019970704128A patent/KR100521655B1/ko not_active IP Right Cessation
- 1996-10-16 BR BR9607167A patent/BR9607167A/pt not_active IP Right Cessation
- 1996-10-16 DE DE69626783T patent/DE69626783T2/de not_active Expired - Lifetime
- 1996-10-16 CA CA002208587A patent/CA2208587C/fr not_active Expired - Fee Related
- 1996-10-16 JP JP51556797A patent/JP4209944B2/ja not_active Expired - Fee Related
- 1996-10-16 CN CN96191610A patent/CN1122689C/zh not_active Expired - Fee Related
- 1996-10-16 EE EE9700130A patent/EE9700130A/xx unknown
- 1996-10-16 EP EP96934920A patent/EP0799280B1/de not_active Expired - Lifetime
- 1996-10-16 AU AU73053/96A patent/AU7305396A/en not_active Abandoned
- 1996-10-16 DK DK96934920T patent/DK0799280T3/da active
- 1996-10-16 AT AT96934920T patent/ATE234898T1/de active
- 1996-10-19 MY MYPI96004353A patent/MY115861A/en unknown
-
1997
- 1997-06-18 NO NO972809A patent/NO309944B1/no not_active IP Right Cessation
-
1998
- 1998-10-16 US US08/860,153 patent/US5883162A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
CA2208587A1 (fr) | 1997-04-24 |
CN1169745A (zh) | 1998-01-07 |
MX9704597A (es) | 1997-10-31 |
NO972809D0 (no) | 1997-06-18 |
JPH10511737A (ja) | 1998-11-10 |
CZ291716B6 (cs) | 2003-05-14 |
BR9607167A (pt) | 1997-11-11 |
ATE234898T1 (de) | 2003-04-15 |
CA2208587C (fr) | 2006-12-12 |
DK0799280T3 (da) | 2003-07-14 |
KR100521655B1 (ko) | 2005-12-27 |
EP0799280A1 (de) | 1997-10-08 |
CZ192797A3 (en) | 1997-10-15 |
EE9700130A (et) | 1997-12-15 |
FR2740140B1 (fr) | 1997-11-21 |
ES2195015T3 (es) | 2003-12-01 |
US5883162A (en) | 1999-03-16 |
PL320795A1 (en) | 1997-10-27 |
EP0799280B1 (de) | 2003-03-19 |
FR2740140A1 (fr) | 1997-04-25 |
WO1997014754A1 (fr) | 1997-04-24 |
JP4209944B2 (ja) | 2009-01-14 |
CN1122689C (zh) | 2003-10-01 |
KR987000376A (ko) | 1998-03-30 |
NO972809L (no) | 1997-08-18 |
DE69626783D1 (de) | 2003-04-24 |
AU7305396A (en) | 1997-05-07 |
DE69626783T2 (de) | 2004-02-12 |
MY115861A (en) | 2003-09-30 |
PL187259B1 (pl) | 2004-06-30 |
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