DK176109B1 - Fremgangsmåde til fremstilling af bitumen-polymerpræparater, samt ved fremgangsmåden opnåede sådanne præparater - Google Patents

Fremgangsmåde til fremstilling af bitumen-polymerpræparater, samt ved fremgangsmåden opnåede sådanne præparater Download PDF

Info

Publication number: DK176109B1
Authority: DK; Denmark
Prior art keywords: bitumen; weight; stock solution; process according; copolymer
Prior art date: 1988-09-09

Application number

DK199001136A

Other languages

Danish (da)

English (en)

Other versions

DK113690D0 (da

DK113690A (da

Inventor

Jean-Pascal Planche

Francois Travers

Annie Zins

Original Assignee

Elf France

Priority date (The priority date 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 date listed.)

1988-09-09

Filing date

1990-05-08

Publication date

2006-07-17

1990-05-08 Application filed by Elf France filed Critical Elf France

1990-05-08 Publication of DK113690D0 publication Critical patent/DK113690D0/da

1990-06-28 Publication of DK113690A publication Critical patent/DK113690A/da

2006-07-17 Application granted granted Critical

2006-07-17 Publication of DK176109B1 publication Critical patent/DK176109B1/da

Links

229920000642 polymer Polymers 0.000 title claims description 66
238000000034 method Methods 0.000 title claims description 44
238000002360 preparation method Methods 0.000 title claims description 42
239000010426 asphalt Substances 0.000 claims description 99
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 72
239000000203 mixture Substances 0.000 claims description 65
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 58
229920001577 copolymer Polymers 0.000 claims description 58
239000007822 coupling agent Substances 0.000 claims description 50
229910052717 sulfur Inorganic materials 0.000 claims description 50
239000011593 sulfur Substances 0.000 claims description 50
239000011550 stock solution Substances 0.000 claims description 46
150000002430 hydrocarbons Chemical class 0.000 claims description 39
239000004215 Carbon black (E152) Substances 0.000 claims description 26
229930195733 hydrocarbon Natural products 0.000 claims description 26
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 24
239000003921 oil Substances 0.000 claims description 23
238000003756 stirring Methods 0.000 claims description 22
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 20
238000004073 vulcanization Methods 0.000 claims description 17
150000001993 dienes Chemical class 0.000 claims description 15
229920001021 polysulfide Polymers 0.000 claims description 15
239000005077 polysulfide Substances 0.000 claims description 14
150000008117 polysulfides Polymers 0.000 claims description 14
238000004821 distillation Methods 0.000 claims description 12
239000003208 petroleum Substances 0.000 claims description 12
230000035515 penetration Effects 0.000 claims description 9
238000000576 coating method Methods 0.000 claims description 8
150000001875 compounds Chemical class 0.000 claims description 8
239000002904 solvent Substances 0.000 claims description 8
125000003118 aryl group Chemical group 0.000 claims description 7
229920001400 block copolymer Polymers 0.000 claims description 7
229920006395 saturated elastomer Polymers 0.000 claims description 7
239000003795 chemical substances by application Substances 0.000 claims description 6
239000000243 solution Substances 0.000 claims description 6
238000004519 manufacturing process Methods 0.000 claims description 5
125000004434 sulfur atom Chemical group 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 4
150000002019 disulfides Chemical class 0.000 claims description 4
125000000753 cycloalkyl group Chemical group 0.000 claims description 3
230000001747 exhibiting effect Effects 0.000 claims description 3
125000001424 substituent group Chemical group 0.000 claims description 3
BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 claims description 2
YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 claims description 2
239000011280 coal tar Substances 0.000 claims description 2
229910052757 nitrogen Inorganic materials 0.000 claims description 2
125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
235000013311 vegetables Nutrition 0.000 claims description 2
239000004615 ingredient Substances 0.000 claims 1
150000003568 thioethers Chemical class 0.000 claims 1
230000032683 aging Effects 0.000 description 10
238000012360 testing method Methods 0.000 description 8
238000007669 thermal treatment Methods 0.000 description 6
229920001971 elastomer Polymers 0.000 description 4
239000007788 liquid Substances 0.000 description 4
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 4
229960002447 thiram Drugs 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 3
239000000470 constituent Substances 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000000806 elastomer Substances 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
238000002156 mixing Methods 0.000 description 3
238000003860 storage Methods 0.000 description 3
238000009864 tensile test Methods 0.000 description 3
-1 zinc stearate Chemical compound 0.000 description 3
UXDMWYANCHMSJX-UHFFFAOYSA-N (benzyltrisulfanyl)methylbenzene Chemical compound C=1C=CC=CC=1CSSSCC1=CC=CC=C1 UXDMWYANCHMSJX-UHFFFAOYSA-N 0.000 description 2
YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
FLLHZLOYVPKTTJ-UHFFFAOYSA-N dibenzyl tetrasulphide Natural products C=1C=CC=CC=1CSSSSCC1=CC=CC=C1 FLLHZLOYVPKTTJ-UHFFFAOYSA-N 0.000 description 2
AUZONCFQVSMFAP-UHFFFAOYSA-N disulfiram Chemical compound CCN(CC)C(=S)SSC(=S)N(CC)CC AUZONCFQVSMFAP-UHFFFAOYSA-N 0.000 description 2
239000007858 starting material Substances 0.000 description 2
230000003068 static effect Effects 0.000 description 2
229920006301 statistical copolymer Polymers 0.000 description 2
QAZLUNIWYYOJPC-UHFFFAOYSA-M sulfenamide Chemical compound [Cl-].COC1=C(C)C=[N+]2C3=NC4=CC=C(OC)C=C4N3SCC2=C1C QAZLUNIWYYOJPC-UHFFFAOYSA-M 0.000 description 2
150000003463 sulfur Chemical class 0.000 description 2
125000003837 (C1-C20) alkyl group Chemical group 0.000 description 1
125000006736 (C6-C20) aryl group Chemical group 0.000 description 1
QZXIAZMRRQBSFL-UHFFFAOYSA-N (benzylpentasulfanyl)methylbenzene Chemical compound C=1C=CC=CC=1CSSSSSCC1=CC=CC=C1 QZXIAZMRRQBSFL-UHFFFAOYSA-N 0.000 description 1
PYHGXXMMSWMRDF-UHFFFAOYSA-N (phenyltetrasulfanyl)benzene Chemical compound C=1C=CC=CC=1SSSSC1=CC=CC=C1 PYHGXXMMSWMRDF-UHFFFAOYSA-N 0.000 description 1
WYHWGJJOJLOJSZ-UHFFFAOYSA-N (phenyltrisulfanyl)benzene Chemical compound C=1C=CC=CC=1SSSC1=CC=CC=C1 WYHWGJJOJLOJSZ-UHFFFAOYSA-N 0.000 description 1
GAYUSSOCODCSNF-UHFFFAOYSA-N 1-(dodecyldisulfanyl)dodecane Chemical compound CCCCCCCCCCCCSSCCCCCCCCCCCC GAYUSSOCODCSNF-UHFFFAOYSA-N 0.000 description 1
PVEOHIPIGXRZSI-UHFFFAOYSA-N 1-(hexadecylpentasulfanyl)hexadecane Chemical compound CCCCCCCCCCCCCCCCSSSSSCCCCCCCCCCCCCCCC PVEOHIPIGXRZSI-UHFFFAOYSA-N 0.000 description 1
NWBKTDHIFNRHIR-UHFFFAOYSA-N 1-(hexadecyltetrasulfanyl)hexadecane Chemical compound CCCCCCCCCCCCCCCCSSSSCCCCCCCCCCCCCCCC NWBKTDHIFNRHIR-UHFFFAOYSA-N 0.000 description 1
QAHRXZPUWCQRAC-UHFFFAOYSA-N 1-(octylpentasulfanyl)octane Chemical compound CCCCCCCCSSSSSCCCCCCCC QAHRXZPUWCQRAC-UHFFFAOYSA-N 0.000 description 1
VAKWIIMMZSTGAI-UHFFFAOYSA-N 1-(octyltetrasulfanyl)octane Chemical compound CCCCCCCCSSSSCCCCCCCC VAKWIIMMZSTGAI-UHFFFAOYSA-N 0.000 description 1
ABUMGKFJCJEUNA-UHFFFAOYSA-N 1-(octyltrisulfanyl)octane Chemical compound CCCCCCCCSSSCCCCCCCC ABUMGKFJCJEUNA-UHFFFAOYSA-N 0.000 description 1
VVFVRTNNLLZXAL-UHFFFAOYSA-N 2-(2-methylphenyl)guanidine Chemical compound CC1=CC=CC=C1N=C(N)N VVFVRTNNLLZXAL-UHFFFAOYSA-N 0.000 description 1
HLBZWYXLQJQBKU-UHFFFAOYSA-N 4-(morpholin-4-yldisulfanyl)morpholine Chemical compound C1COCCN1SSN1CCOCC1 HLBZWYXLQJQBKU-UHFFFAOYSA-N 0.000 description 1
NRKOJWAMCFSTTK-UHFFFAOYSA-N 5,5,6,6-tetramethyltetrathiane Chemical compound CC1(C)SSSSC1(C)C NRKOJWAMCFSTTK-UHFFFAOYSA-N 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
KUGRPPRAQNPSQD-UHFFFAOYSA-N OOOOO Chemical compound OOOOO KUGRPPRAQNPSQD-UHFFFAOYSA-N 0.000 description 1
MOMWFXLCFJOAFX-UHFFFAOYSA-N OOOOOOOO Chemical compound OOOOOOOO MOMWFXLCFJOAFX-UHFFFAOYSA-N 0.000 description 1
229920002367 Polyisobutene Polymers 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000012190 activator Substances 0.000 description 1
125000002723 alicyclic group Chemical group 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
125000000732 arylene group Chemical group 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
229920005549 butyl rubber Polymers 0.000 description 1
DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
239000013256 coordination polymer Substances 0.000 description 1
230000008878 coupling Effects 0.000 description 1
238000010168 coupling process Methods 0.000 description 1
238000005859 coupling reaction Methods 0.000 description 1
125000002993 cycloalkylene group Chemical group 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000004956 cyclohexylene group Chemical group 0.000 description 1
JLQNHALFVCURHW-UHFFFAOYSA-N cyclooctasulfur Chemical compound S1SSSSSSS1 JLQNHALFVCURHW-UHFFFAOYSA-N 0.000 description 1
PGAXJQVAHDTGBB-UHFFFAOYSA-N dibutylcarbamothioylsulfanyl n,n-dibutylcarbamodithioate Chemical compound CCCCN(CCCC)C(=S)SSC(=S)N(CCCC)CCCC PGAXJQVAHDTGBB-UHFFFAOYSA-N 0.000 description 1
REQPQFUJGGOFQL-UHFFFAOYSA-N dimethylcarbamothioyl n,n-dimethylcarbamodithioate Chemical compound CN(C)C(=S)SC(=S)N(C)C REQPQFUJGGOFQL-UHFFFAOYSA-N 0.000 description 1
229940096818 dipentamethylenethiuram disulfide Drugs 0.000 description 1
239000012990 dithiocarbamate Substances 0.000 description 1
125000003438 dodecyl 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])C([H])([H])C([H])([H])* 0.000 description 1
HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000013529 heat transfer fluid Substances 0.000 description 1
238000010438 heat treatment Methods 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
239000008240 homogeneous mixture Substances 0.000 description 1
239000012456 homogeneous solution Substances 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
125000001400 nonyl group Chemical group [H]C([*])([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])[H] 0.000 description 1
125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
KNBRWWCHBRQLNY-UHFFFAOYSA-N piperidine-1-carbothioylsulfanyl piperidine-1-carbodithioate Chemical compound C1CCCCN1C(=S)SSC(=S)N1CCCCC1 KNBRWWCHBRQLNY-UHFFFAOYSA-N 0.000 description 1
229920001084 poly(chloroprene) Polymers 0.000 description 1
229920000636 poly(norbornene) polymer Polymers 0.000 description 1
229920001083 polybutene Polymers 0.000 description 1
229920001195 polyisoprene Polymers 0.000 description 1
229920000193 polymethacrylate Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000004321 preservation Methods 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
239000002344 surface layer Substances 0.000 description 1
229920001897 terpolymer Polymers 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
125000005628 tolylene group Chemical group 0.000 description 1
XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L95/00—Compositions of bituminous materials, e.g. asphalt, tar, pitch

Landscapes

Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Organic Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Civil Engineering (AREA)
Structural Engineering (AREA)
Materials Engineering (AREA)
Chemical Kinetics & Catalysis (AREA)
Health & Medical Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Compositions Of Macromolecular Compounds (AREA)
Processes Of Treating Macromolecular Substances (AREA)
Road Paving Structures (AREA)
Sealing Material Composition (AREA)
Paints Or Removers (AREA)

DK199001136A 1988-09-09 1990-05-08 Fremgangsmåde til fremstilling af bitumen-polymerpræparater, samt ved fremgangsmåden opnåede sådanne præparater DK176109B1 (da)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
FR8811825		1988-09-09
FR8811825A FR2636340B1 (fr)	1988-09-09	1988-09-09	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
FR8900453		1989-01-16
PCT/FR1989/000453 WO1990002776A1 (fr)	1988-09-09	1989-09-08	Procede de preparaton de compositions bitume-polymere

Publications (3)

Publication Number	Publication Date
DK113690D0 DK113690D0 (da)	1990-05-08
DK113690A DK113690A (da)	1990-06-28
DK176109B1 true DK176109B1 (da)	2006-07-17

Family

ID=9369877

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DK199001136A DK176109B1 (da)	1988-09-09	1990-05-08	Fremgangsmåde til fremstilling af bitumen-polymerpræparater, samt ved fremgangsmåden opnåede sådanne præparater

Country Status (13)

Country	Link
EP (1)	EP0360656B1 (de)
JP (1)	JP2731442B2 (de)
AR (1)	AR245471A1 (de)
AT (1)	ATE99723T1 (de)
AU (1)	AU628390B2 (de)
BR (1)	BR8907085A (de)
CA (1)	CA1341275C (de)
DE (1)	DE68912044T2 (de)
DK (1)	DK176109B1 (de)
ES (1)	ES2062069T3 (de)
FR (1)	FR2636340B1 (de)
NO (1)	NO178580C (de)
WO (1)	WO1990002776A1 (de)

Families Citing this family (46)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2649117B1 (fr) *	1989-06-30	1992-12-31	Elf France	Composition bitume/polymere presentant une adhesivite se conservant au stockage a temperature elevee et procede de preparation d'une telle composition
FR2670497B1 (fr) *	1990-12-18	1994-05-13	Elf France	Composante bitume/polymere utilisable pour former des compositions bitume/polymere a tres faible susceptibilite thermique applicables a la realisation de revetements.
DE69124998T2 (de) *	1990-12-18	1997-12-04	Elf Antar France, Courbevoie	Bitumen-polymer-komponente für die herstellung von bitumen-polymere-zusammensetzungen mit niedriger thermischer suszeptibilität
FR2670498B1 (fr) *	1990-12-18	1994-04-15	Elf France	Composition bitume/polymere presentant une tres faible susceptibilite thermique, procede pour sa preparation et application de cette composition a la realisation de revetements.
US5130354A (en) *	1991-05-13	1992-07-14	Shell Oil Company	Asphalt-diene polymer composition with improved adhesion to polar materials
US5494966A (en) *	1991-09-30	1996-02-27	Univ Toronto	In-situ stabilized 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.
FR2703063A1 (fr) *	1993-03-26	1994-09-30	Elf Antar France	Compositions bitume/polymère non gélifiables et stables au stockage à température élevée, leur procédé de préparation et leur application à la production de liants bitume/polymère pour revêtements.
CA2112128A1 (en) *	1992-04-23	1993-11-11	Dennis Krivohlavek	Bitumen/polymer composition vulcanisable at temperatures below 100°c, its preparation and its use
FR2693490B1 (fr) *	1992-07-07	1994-09-02	Elf Antar France	Système perfectionné anti-remontée de fissures intercalé entre la couche de structure et la couche de roulement d'une chaussée et procédé pour la réalisation d'un tel système.
ES2054579B1 (es) *	1992-11-20	1995-02-16	Repsol Petroleo Sa	Procedimiento de preparacion de composiciones complejas hidrocarbonado-polimericas reticuladas.
FR2703064B1 (fr) *	1993-03-26	1996-06-07	Elf Antar France	Compositions bitume/polymère non gélifiables et stables au stockage à température élevée, leur procédé de préparation et leur application à la production de liants bitume/polymère pour revêtements .
USH1484H (en) *	1993-11-30	1995-09-05	Shell Oil Company	Method for obtaining polymer/bitumen blends with improved stability and polymer efficiency
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.
FR2726830B1 (fr) *	1994-11-10	1996-12-20	Elf Aquitaine	Procede de preparation de compositions bitume/polymere pour la realisation de revetements et solution mere de polymere pour cette preparation
TW294704B (de) *	1995-02-28	1997-01-01	Grace W R & Co
GB2301107A (en) *	1995-05-22	1996-11-27	Shell Int Research	Preparation process for polymer-modified bitumen
ZA963986B (en) *	1995-05-22	1996-11-25	Shell Int Research	Preparation process for polymer-modified bitumen
US5719216A (en) *	1995-05-22	1998-02-17	Shell Oil Company	Preparation process for polymer-modified bitumen
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1988
- 1988-09-09 FR FR8811825A patent/FR2636340B1/fr not_active Expired - Lifetime
1989
- 1989-09-08 AR AR89314869A patent/AR245471A1/es active
- 1989-09-08 DE DE68912044T patent/DE68912044T2/de not_active Expired - Lifetime
- 1989-09-08 JP JP1509452A patent/JP2731442B2/ja not_active Expired - Lifetime
- 1989-09-08 AT AT89402453T patent/ATE99723T1/de not_active IP Right Cessation
- 1989-09-08 AU AU42176/89A patent/AU628390B2/en not_active Ceased
- 1989-09-08 WO PCT/FR1989/000453 patent/WO1990002776A1/fr not_active Ceased
- 1989-09-08 CA CA000610835A patent/CA1341275C/fr not_active Expired - Fee Related
- 1989-09-08 BR BR898907085A patent/BR8907085A/pt not_active IP Right Cessation
- 1989-09-08 ES ES89402453T patent/ES2062069T3/es not_active Expired - Lifetime
- 1989-09-08 EP EP89402453A patent/EP0360656B1/de not_active Expired - Lifetime
1990
- 1990-05-08 NO NO902038A patent/NO178580C/no unknown
- 1990-05-08 DK DK199001136A patent/DK176109B1/da not_active IP Right Cessation

Also Published As

Publication number	Publication date
BR8907085A (pt)	1990-10-02
NO178580B (no)	1996-01-15
EP0360656B1 (de)	1994-01-05
NO902038L (no)	1990-07-06
CA1341275C (fr)	2001-07-10
WO1990002776A1 (fr)	1990-03-22
FR2636340B1 (fr)	1992-04-17
DE68912044T2 (de)	1994-08-11
NO178580C (no)	1996-04-24
AU628390B2 (en)	1992-09-17
ES2062069T3 (es)	1994-12-16
DK113690D0 (da)	1990-05-08
DE68912044D1 (de)	1994-02-17
JPH03501035A (ja)	1991-03-07
AU4217689A (en)	1990-04-02
FR2636340A1 (fr)	1990-03-16
DK113690A (da)	1990-06-28
JP2731442B2 (ja)	1998-03-25
EP0360656A1 (de)	1990-03-28
AR245471A1 (es)	1994-01-31
ATE99723T1 (de)	1994-01-15
NO902038D0 (no)	1990-05-08

Legal Events

Date	Code	Title	Description
2009-09-28	PUP	Patent expired

Publication	Publication Date	Title
DK176109B1 (da)	2006-07-17	Fremgangsmåde til fremstilling af bitumen-polymerpræparater, samt ved fremgangsmåden opnåede sådanne præparater
DK169877B1 (da)	1995-03-20	Fremgangsmåde til fremstilling af bitumen-polymer-sammensætninger, anvendelse af sammensætningerne til fremstilling af belægninger, især overfladebelægninger til veje, og polymermoderopløsninger til brug ved fremstilling af sådanne bitumen-polymersammensætninger
US5874492A (en)	1999-02-23	Process for the preparation of bitumen-polymer compositions, application of the compositions obtained to the production of coatings and polymer master solution for obtaining the said compositions
CA2208253C (fr)	2006-10-10	Procede de preparation de compositions bitume/polymere a caractere multigrade renforce et application des compositions obtenues a la production de liants bitume/polymere pour revetements
CA2103811C (en)	2001-07-03	Rubber processing oil and rubber products containing it
DK169260B1 (da)	1994-09-26	Fremgangsmåde til fremstilling af en flydende bitumen-polymerblanding
JP4073951B2 (ja)	2008-04-09	ビチューメン／ポリマー組成物の製造と使用
NO309195B1 (no)	2000-12-27	Fremgangsmåte ved fremstilling av bitumen/polymerblandinger samt anvendelse derav, samt stamlösning til bruk i fremstillingen
NO311436B1 (no)	2001-11-26	Fremgangsmåte ved fremstilling av polymer/bitumen sammensetninger og deres anvendelse i beleggingsmaterialer, samtstamlösninger for anvendelse ved fremstilling av sammensetningene
NO864098L (no)	1987-04-21	Forbedret veidekkingsasfalt.
JPH0519585B2 (de)	1993-03-17
US5428085A (en)	1995-06-27	Bitumen-polymer compositions, their method of preparation and their uses
US6767939B2 (en)	2004-07-27	Method for preparation of stable bitumen polymer compositions
US6852779B1 (en)	2005-02-08	Method for the production of cross-linked and/or functionalized bitumen/polymer compositions and use of said compositions in coverings
US2814595A (en)	1957-11-26	Open gear lubricants
US3265517A (en)	1966-08-09	Hydrodechlorination processes and products of chlorinated asphaltenes and thermoplastic hydrocarbon resins
EP0559462B1 (de)	2000-04-26	Neuer mit Kunststoff modifizierter, oxidierter Asphalt und Methoden zu seiner Herstellung
KR100558496B1 (ko)	2006-10-24	중합체/비투먼 조성물의 제조방법 및 외장재에의 응용
US1875502A (en)	1932-09-06	Harold j
EP1205520A1 (de)	2002-05-15	Verfahren zur Herstellung von stabilen Mischungen von Bitumen und Polymeren
KR20000022071A (ko)	2000-04-25	작용화된 엘라스토머/비투먼 조성물의 제조방법 및 외장재에의응용