BE477430A - - Google Patents
Info
- Publication number
- BE477430A BE477430A BE477430DA BE477430A BE 477430 A BE477430 A BE 477430A BE 477430D A BE477430D A BE 477430DA BE 477430 A BE477430 A BE 477430A
- Authority
- BE
- Belgium
- Prior art keywords
- sep
- polymer
- carbon
- diolefin
- olefin
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 claims description 47
- 239000000203 mixture Substances 0.000 claims description 25
- 229910052799 carbon Inorganic materials 0.000 claims description 18
- 229920001971 elastomer Polymers 0.000 claims description 17
- 239000004014 plasticizer Substances 0.000 claims description 17
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 16
- 229920001577 copolymer Polymers 0.000 claims description 16
- 150000001993 dienes Chemical class 0.000 claims description 15
- 239000000806 elastomer Substances 0.000 claims description 14
- 150000001336 alkenes Chemical class 0.000 claims description 11
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 11
- 238000007334 copolymerization reaction Methods 0.000 claims description 9
- 239000000126 substance Substances 0.000 claims description 6
- 238000010348 incorporation Methods 0.000 claims description 3
- 230000009467 reduction Effects 0.000 claims description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 241001441571 Hiodontidae Species 0.000 description 5
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- 230000008602 contraction Effects 0.000 description 5
- 239000007858 starting material Substances 0.000 description 5
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 230000008961 swelling Effects 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- 238000005452 bending Methods 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- YQCIWBXEVYWRCW-UHFFFAOYSA-N methane;sulfane Chemical compound C.S YQCIWBXEVYWRCW-UHFFFAOYSA-N 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 238000004073 vulcanization Methods 0.000 description 2
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical group C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 1
- 241000238876 Acari Species 0.000 description 1
- 229910015900 BF3 Inorganic materials 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
- 238000012773 Laboratory assay Methods 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241000288936 Perodicticus potto Species 0.000 description 1
- 206010041235 Snoring Diseases 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 238000005411 Van der Waals force Methods 0.000 description 1
- 238000004378 air conditioning Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- -1 butadiene-1-5 Natural products 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 229920005684 linear copolymer Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 150000005673 monoalkenes Chemical group 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
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 239000011701 zinc Substances 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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F36/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F36/02—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F36/04—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE477430A true BE477430A (instruction) |
Family
ID=125503
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE477430D BE477430A (instruction) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE477430A (instruction) |
-
0
- BE BE477430D patent/BE477430A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| FR2682681A1 (fr) | Elastomere segmente a hautes performances. | |
| FR2961817A1 (fr) | Caoutchouc de copolymere ternaire ayant une structure sequencee en forme d'etoile, procede de preparation et utilisation correspondante | |
| EP1242486B1 (fr) | Elastomeres flouorosulfones a faible tg a base d'hexafloropropene et ne contenant ni du tetrafluoroethylene, ni de groupement siloxane | |
| FR2651787A1 (fr) | Noirs de carbone au four utiles dans des compositions de caoutchouc. | |
| WO2020074806A1 (fr) | Composition de caoutchouc | |
| WO2017103544A1 (fr) | Copolymere d'ethylene et de butadiene de microstructure homogene | |
| FR2611209A1 (fr) | Corps composites caoutchouc-cable | |
| CA2328433A1 (fr) | Elastomeres nitriles fluorosulfones reticulables a faible tg a base de fluorure de vinylidene et ne contenant ni du tetrafluoroethylene ni de groupement siloxane | |
| FR2464279A1 (fr) | Compositions de caoutchouc a base de polybutadiene | |
| Van Duin et al. | Effect of third monomer type and content on peroxide crosslinking efficiency of EPDM | |
| BE477430A (instruction) | ||
| FR2619384A1 (fr) | Procede de production d'une resine fluoree souple polymerisee par greffe | |
| FR2465703A1 (fr) | Alcoolates tertiaires de baryum, leur preparation, compositions en renfermant utilisables dans des polymerisations anioniques et procede de polymerisation de monomeres ethyleniques et de monomeres heterocycliques | |
| CN111875743B (zh) | 一种增强改性橡胶及其制备工艺 | |
| FR2497208A1 (fr) | Caoutchouc polymere a plusieurs composants | |
| EP3541635B1 (fr) | Pneumatique comprenant un copolymère à blocs comprenant un bloc élastomère avec des unités isobutylène et halogénoalkylstyrène | |
| FR3010079A1 (fr) | Copolymeres derives du polyfluorure de vinylidene | |
| EP0055698B1 (fr) | Adjuvant pour améliorer la résistance à la fracture du polychlorure de vinyle, procédé de fabrication de cet adjuvant et utilisation | |
| CN108485076A (zh) | 一种含受阻酚的新型硅烷偶联剂改性碳酸钙的聚烯烃及其制备方法 | |
| BE549696A (instruction) | ||
| BE698518A (instruction) | ||
| WO2023117840A1 (fr) | Polymère portant des groupes pendants fonctionnels particuliers époxy | |
| BE840097R (fr) | Procede de preparation de caoutchoucs synthetiques | |
| FR3058726A1 (fr) | Couche interne etanche de pneumatique comprenant une matrice elastomerique a base d'un copolymere a blocs comprenant un bloc elastomere avec des unites isobutylene et halogenoalkylstyrene | |
| WO2024160940A1 (fr) | Lame d'essuyage pour balai d'essuie-glace |