BE551803A - - Google Patents
Info
- Publication number
- BE551803A BE551803A BE551803DA BE551803A BE 551803 A BE551803 A BE 551803A BE 551803D A BE551803D A BE 551803DA BE 551803 A BE551803 A BE 551803A
- Authority
- BE
- Belgium
- Prior art keywords
- additive
- carbon atoms
- sep
- parts
- tetramethylethylenedioxy
- Prior art date
Links
- 229920001296 polysiloxane Polymers 0.000 claims description 66
- 229920000591 gum Polymers 0.000 claims description 53
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 47
- 239000000654 additive Substances 0.000 claims description 39
- 230000000996 additive Effects 0.000 claims description 30
- -1 tetramethylethylenedioxy Chemical group 0.000 claims description 28
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 24
- 239000000203 mixture Substances 0.000 claims description 23
- 239000000377 silicon dioxide Substances 0.000 claims description 21
- IVDFJHOHABJVEH-UHFFFAOYSA-N Pinacol Chemical compound CC(C)(O)C(C)(C)O IVDFJHOHABJVEH-UHFFFAOYSA-N 0.000 claims description 19
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 16
- 229920002379 silicone rubber Polymers 0.000 claims description 15
- 125000003118 aryl group Chemical group 0.000 claims description 12
- 239000004945 silicone rubber Substances 0.000 claims description 12
- UQEAIHBTYFGYIE-UHFFFAOYSA-N Hexamethyldisiloxane Chemical group C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 9
- 238000009835 boiling Methods 0.000 claims description 8
- BLRPTPMANUNPDV-UHFFFAOYSA-N silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 8
- 229910000077 silane Inorganic materials 0.000 claims description 8
- 125000004435 hydrogen atoms Chemical class [H]* 0.000 claims description 6
- 125000003342 alkenyl group Chemical group 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 239000002245 particle Substances 0.000 claims description 5
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- UBHZUDXTHNMNLD-UHFFFAOYSA-N dimethylsilane Chemical compound C[SiH2]C UBHZUDXTHNMNLD-UHFFFAOYSA-N 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 238000009833 condensation Methods 0.000 claims description 3
- 230000005494 condensation Effects 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 2
- 230000000875 corresponding Effects 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 3
- 125000004429 atoms Chemical group 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 1
- ZQDPJFUHLCOCRG-UHFFFAOYSA-N hex-3-ene Chemical group CCC=CCC ZQDPJFUHLCOCRG-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 229920001098 polystyrene-block-poly(ethylene/propylene) Polymers 0.000 description 85
- 229920001971 elastomer Polymers 0.000 description 28
- 239000000806 elastomer Substances 0.000 description 27
- 235000019589 hardness Nutrition 0.000 description 18
- 238000004073 vulcanization Methods 0.000 description 15
- 238000002360 preparation method Methods 0.000 description 12
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 8
- 238000010992 reflux Methods 0.000 description 8
- 239000000047 product Substances 0.000 description 7
- ZMANZCXQSJIPKH-UHFFFAOYSA-N triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 7
- AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- 229910002012 Aerosil® Inorganic materials 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 4
- LIKFHECYJZWXFJ-UHFFFAOYSA-N Dimethyldichlorosilane Chemical compound C[Si](C)(Cl)Cl LIKFHECYJZWXFJ-UHFFFAOYSA-N 0.000 description 3
- IJOOHPMOJXWVHK-UHFFFAOYSA-N Trimethylsilyl chloride Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 150000004756 silanes Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000005051 trimethylchlorosilane Substances 0.000 description 3
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- KOPOQZFJUQMUML-UHFFFAOYSA-N Chlorosilane Chemical class Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 2
- 239000005046 Chlorosilane Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Incidol Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating Effects 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
- BYLOHCRAPOSXLY-UHFFFAOYSA-N dichloro(diethyl)silane Chemical compound CC[Si](Cl)(Cl)CC BYLOHCRAPOSXLY-UHFFFAOYSA-N 0.000 description 2
- GNEPOXWQWFSSOU-UHFFFAOYSA-N dichloro-methyl-phenylsilane Chemical compound C[Si](Cl)(Cl)C1=CC=CC=C1 GNEPOXWQWFSSOU-UHFFFAOYSA-N 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000012258 stirred mixture Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- LEQNJUZEJVNIIP-UHFFFAOYSA-N 2,3-dimethylbutane-2,3-diol;hexahydrate Chemical compound O.O.O.O.O.O.CC(C)(O)C(C)(C)O LEQNJUZEJVNIIP-UHFFFAOYSA-N 0.000 description 1
- ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-Aminopyridine Chemical compound NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N Disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 241001182492 Nes Species 0.000 description 1
- 101710023774 SEMA4C Proteins 0.000 description 1
- 125000005741 alkyl alkenyl group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group 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
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- OSXYHAQZDCICNX-UHFFFAOYSA-N dichloro(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](Cl)(Cl)C1=CC=CC=C1 OSXYHAQZDCICNX-UHFFFAOYSA-N 0.000 description 1
- UAHXIHWRAUNYLA-UHFFFAOYSA-N ethyl-dimethyl-phenylsilane Chemical compound CC[Si](C)(C)C1=CC=CC=C1 UAHXIHWRAUNYLA-UHFFFAOYSA-N 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- 238000011068 load Methods 0.000 description 1
- LAQFLZHBVPULPL-UHFFFAOYSA-N methyl(phenyl)silicon Chemical compound C[Si]C1=CC=CC=C1 LAQFLZHBVPULPL-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L na2so4 Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000003014 reinforcing Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 125000005624 silicic acid group Chemical group 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE551803A true BE551803A (no) |
Family
ID=177208
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE551803D BE551803A (no) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE551803A (no) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1669965B1 (de) * | 1966-06-23 | 1971-03-04 | Dow Corning | Molekuelvergroesserungsinhibitoren in haertbaren gemischen aus organosiliciumverbindungen |
| US4104239A (en) * | 1976-03-05 | 1978-08-01 | Rhone-Poulenc Industries | Organopolysiloxane compositions transformable into elastomers without use of vulcanizing agents |
-
0
- BE BE551803D patent/BE551803A/fr unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1669965B1 (de) * | 1966-06-23 | 1971-03-04 | Dow Corning | Molekuelvergroesserungsinhibitoren in haertbaren gemischen aus organosiliciumverbindungen |
| US4104239A (en) * | 1976-03-05 | 1978-08-01 | Rhone-Poulenc Industries | Organopolysiloxane compositions transformable into elastomers without use of vulcanizing agents |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4057566A (en) | Fluorocarbon siloxane compositions | |
| EP1326871B1 (fr) | Organosilane polyfonctionnel utilisable comme agent de couplage et son procede d'obtention | |
| FR2487367A1 (fr) | Composition formee d'un polysilane contenant des radicaux alkyle ou phenyle, sa preparation et son application a la fabrication de matieres et articles ceramiques a base de carbure de silicium | |
| DE2642833C3 (de) | Oxysilan-Verbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung | |
| JPS5980464A (ja) | 改善された耐溶剤性加硫性シリコ−ンゴム組成物 | |
| EP0147323A2 (fr) | Composition polyorganosiloxanique durcissant en élastomère etcomportant un catalyseur à l'étain chelate. | |
| FR2487363A1 (fr) | Composition a base d'un polysilane a groupes trimethylsiloxy, sa preparation et son application a la fabrication de matieres et articles ceramiques a base de carbure de silicium | |
| CN108641086A (zh) | 一种含季铵盐硅橡胶生胶及其合成与在制备本征季铵盐型防霉抗菌密封胶中的应用 | |
| FR2487364A1 (fr) | Composition a base d'un polysilane contenant des atomes d'hydrogene lies au silicium, sa preparation et son application a la fabrication de matieres et articles ceramiques a base de carbure de silicium | |
| BE560351A (no) | ||
| FR2487365A1 (fr) | Composition formee d'un polysilane contenant des radicaux alkoxy ou phenoxy, sa preparation et son application a la fabrication de matieres et articles ceramiques a base de carbure de silicium | |
| US4152315A (en) | Bis(polyorganosiloxanyl)amines and their use | |
| BE551803A (no) | ||
| EP0544257A2 (en) | Triorganosiloxydiphenylsilanols and method for preparing same | |
| CA1162677A (fr) | Compositions organopolysiloxaniques pateuses durcissant a chaud en elastomeres | |
| EP0300862A2 (fr) | Composition à base d'un nouveau polycarbosilane, sa préparation et son application à la fabrication de produits et articles céramiques à base de carbure de silicium | |
| EP2531512A1 (de) | Verwendung von polyorganosiloxanen bei der verarbeitung und vulkanisation von kautschuk | |
| JP2697523B2 (ja) | オイルブリード性シリコーンゴム組成物及びその硬化物 | |
| JPS6119659A (ja) | 改善された液状共重合体オルガノシロキサン | |
| JPS5837338B2 (ja) | 網化してエラストマ−になり得る組成物 | |
| US6153781A (en) | Silacyclobutene compounds, methods of preparing same, and polymers formed therefrom | |
| JPH01151591A (ja) | 有機けい素化合物 | |
| JPS5920678B2 (ja) | ハロゲン化オキシシラン化合物およびその製造方法 | |
| EP0325881B1 (fr) | Diorganopolysiloxane à fonction benzylidène-3 camphre | |
| CN113444286B (zh) | 一种加成型液体氟硅橡胶抑制剂及其制备方法 |