NL8105755A - Fenoxyalkoxysilanen. - Google Patents
Fenoxyalkoxysilanen. Download PDFInfo
- Publication number
- NL8105755A NL8105755A NL8105755A NL8105755A NL8105755A NL 8105755 A NL8105755 A NL 8105755A NL 8105755 A NL8105755 A NL 8105755A NL 8105755 A NL8105755 A NL 8105755A NL 8105755 A NL8105755 A NL 8105755A
- Authority
- NL
- Netherlands
- Prior art keywords
- formula
- tree
- silanes
- silane
- alkyl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 13
- 239000012433 hydrogen halide Substances 0.000 claims description 11
- 229910000039 hydrogen halide Inorganic materials 0.000 claims description 11
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 125000003342 alkenyl group Chemical group 0.000 claims description 6
- 150000001282 organosilanes Chemical class 0.000 claims description 5
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 5
- 239000011541 reaction mixture Substances 0.000 claims description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 5
- 229920002554 vinyl polymer Polymers 0.000 claims description 5
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical group 0.000 claims description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000012442 inert solvent Substances 0.000 claims description 2
- 150000001805 chlorine compounds Chemical group 0.000 claims 2
- 125000006727 (C1-C6) alkenyl group Chemical group 0.000 claims 1
- 244000025352 Artocarpus heterophyllus Species 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
- 150000004756 silanes Chemical class 0.000 description 19
- 238000012360 testing method Methods 0.000 description 11
- -1 organosilane compounds Chemical class 0.000 description 10
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 9
- 239000000654 additive Substances 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 9
- 229910000077 silane Inorganic materials 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 8
- 240000005572 Syzygium cordatum Species 0.000 description 7
- 235000006650 Syzygium cordatum Nutrition 0.000 description 7
- 230000000996 additive effect Effects 0.000 description 6
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 5
- 239000007983 Tris buffer Substances 0.000 description 5
- 230000015556 catabolic process Effects 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000009413 insulation Methods 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- NGSXJHBGCYVLMX-UHFFFAOYSA-N ethenyl-tris(2-phenoxyethoxy)silane Chemical compound C=1C=CC=CC=1OCCO[Si](OCCOC=1C=CC=CC=1)(C=C)OCCOC1=CC=CC=C1 NGSXJHBGCYVLMX-UHFFFAOYSA-N 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 239000011810 insulating material Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229960005323 phenoxyethanol Drugs 0.000 description 3
- 229920002959 polymer blend Polymers 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- JMYBSSVCXVQZFN-UHFFFAOYSA-N 1-(2-phenoxyethoxy)ethanol Chemical compound CC(O)OCCOC1=CC=CC=C1 JMYBSSVCXVQZFN-UHFFFAOYSA-N 0.000 description 2
- 238000004566 IR spectroscopy Methods 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 239000007822 coupling agent Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 239000012212 insulator Substances 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- IBIQRJWYUBZGPH-UHFFFAOYSA-N methyl-tris(2-phenoxyethoxy)silane Chemical compound C=1C=CC=CC=1OCCO[Si](OCCOC=1C=CC=CC=1)(C)OCCOC1=CC=CC=C1 IBIQRJWYUBZGPH-UHFFFAOYSA-N 0.000 description 2
- 239000012764 mineral filler Substances 0.000 description 2
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 description 1
- MDVFVXAKHVBTHQ-UHFFFAOYSA-N 1,1-diethoxy-2-phenoxyethanol Chemical compound CCOC(O)(OCC)COC1=CC=CC=C1 MDVFVXAKHVBTHQ-UHFFFAOYSA-N 0.000 description 1
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical group CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- IBLKWZIFZMJLFL-UHFFFAOYSA-N 1-phenoxypropan-2-ol Chemical compound CC(O)COC1=CC=CC=C1 IBLKWZIFZMJLFL-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical class CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 239000005047 Allyltrichlorosilane Substances 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000005540 biological transmission Effects 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
- KLJPJQLKSTTYTK-UHFFFAOYSA-N butyl(chloro)silane Chemical compound CCCC[SiH2]Cl KLJPJQLKSTTYTK-UHFFFAOYSA-N 0.000 description 1
- FQEKAFQSVPLXON-UHFFFAOYSA-N butyl(trichloro)silane Chemical compound CCCC[Si](Cl)(Cl)Cl FQEKAFQSVPLXON-UHFFFAOYSA-N 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- RHIYNXOJXCFKRZ-UHFFFAOYSA-N ethenyl-tris(3-phenoxypropoxy)silane Chemical compound C=1C=CC=CC=1OCCCO[Si](OCCCOC=1C=CC=CC=1)(C=C)OCCCOC1=CC=CC=C1 RHIYNXOJXCFKRZ-UHFFFAOYSA-N 0.000 description 1
- DALOVCFQSACUNZ-UHFFFAOYSA-N ethenyl-tris[2-(2-phenoxyethoxy)ethoxy]silane Chemical compound C=1C=CC=CC=1OCCOCCO[Si](OCCOCCOC=1C=CC=CC=1)(C=C)OCCOCCOC1=CC=CC=C1 DALOVCFQSACUNZ-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- JILYAQNQZZBHNX-UHFFFAOYSA-N ethyl-tris(phenoxymethoxy)silane Chemical compound C=1C=CC=CC=1OCO[Si](OCOC=1C=CC=CC=1)(CC)OCOC1=CC=CC=C1 JILYAQNQZZBHNX-UHFFFAOYSA-N 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007970 homogeneous dispersion Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000010338 mechanical breakdown Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 239000005055 methyl trichlorosilane Substances 0.000 description 1
- URKJEXZZAMQHMR-UHFFFAOYSA-N methyl-tris(1-phenoxypropan-2-yloxy)silane Chemical compound C=1C=CC=CC=1OCC(C)O[Si](C)(OC(C)COC=1C=CC=CC=1)OC(C)COC1=CC=CC=C1 URKJEXZZAMQHMR-UHFFFAOYSA-N 0.000 description 1
- JLUFWMXJHAVVNN-UHFFFAOYSA-N methyltrichlorosilane Chemical compound C[Si](Cl)(Cl)Cl JLUFWMXJHAVVNN-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000001367 organochlorosilanes Chemical class 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- DHFYLDMPSGAGTP-UHFFFAOYSA-N phenoxymethanol Chemical compound OCOC1=CC=CC=C1 DHFYLDMPSGAGTP-UHFFFAOYSA-N 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000005053 propyltrichlorosilane Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 230000001256 tonic effect Effects 0.000 description 1
- KBSUPJLTDMARAI-UHFFFAOYSA-N tribromo(methyl)silane Chemical compound C[Si](Br)(Br)Br KBSUPJLTDMARAI-UHFFFAOYSA-N 0.000 description 1
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 description 1
- HKFSBKQQYCMCKO-UHFFFAOYSA-N trichloro(prop-2-enyl)silane Chemical compound Cl[Si](Cl)(Cl)CC=C HKFSBKQQYCMCKO-UHFFFAOYSA-N 0.000 description 1
- DOEHJNBEOVLHGL-UHFFFAOYSA-N trichloro(propyl)silane Chemical compound CCC[Si](Cl)(Cl)Cl DOEHJNBEOVLHGL-UHFFFAOYSA-N 0.000 description 1
- 239000005052 trichlorosilane Substances 0.000 description 1
- WEHSMFCDAIHNOW-UHFFFAOYSA-N triethyl phenyl silicate Chemical compound CCO[Si](OCC)(OCC)OC1=CC=CC=C1 WEHSMFCDAIHNOW-UHFFFAOYSA-N 0.000 description 1
- TWUPPABVQZQNJZ-UHFFFAOYSA-N tris(2-phenoxyethoxy)silane Chemical class C=1C=CC=CC=1OCCO[SiH](OCCOC=1C=CC=CC=1)OCCOC1=CC=CC=C1 TWUPPABVQZQNJZ-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 239000005050 vinyl trichlorosilane Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/04—Esters of silicic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/541—Silicon-containing compounds containing oxygen
- C08K5/5415—Silicon-containing compounds containing oxygen containing at least one Si—O bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US21901280 | 1980-12-22 | ||
| US06/219,012 US4332957A (en) | 1980-12-22 | 1980-12-22 | Phenoxyalkoxy silanes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL8105755A true NL8105755A (nl) | 1982-07-16 |
Family
ID=22817437
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL8105755A NL8105755A (nl) | 1980-12-22 | 1981-12-21 | Fenoxyalkoxysilanen. |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4332957A (fr) |
| JP (1) | JPS57128695A (fr) |
| BE (1) | BE891587A (fr) |
| BR (1) | BR8108286A (fr) |
| DE (1) | DE3150076A1 (fr) |
| DK (1) | DK567781A (fr) |
| FI (1) | FI814005L (fr) |
| FR (1) | FR2496667B1 (fr) |
| GB (1) | GB2090844B (fr) |
| IT (1) | IT1140373B (fr) |
| LU (1) | LU83845A1 (fr) |
| NL (1) | NL8105755A (fr) |
| NO (1) | NO814364L (fr) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0109797A3 (fr) * | 1982-11-18 | 1984-06-27 | Dow Corning Corporation | Compositions de polymères résistantes à l'arborescence sous l'influence de l'eau ou de la tension électrique |
| EP0114495A3 (fr) * | 1982-12-27 | 1984-10-17 | Dow Corning Corporation | Additifs contre les arborescences |
| US4840983A (en) * | 1986-05-23 | 1989-06-20 | Dow Corning Corporation | Anti-treeing additives |
| US5110971A (en) * | 1989-07-05 | 1992-05-05 | Aristech Chemical Corporation | Silyl derivatives of eugenol |
| US5206323A (en) * | 1989-07-05 | 1993-04-27 | Hays Mary K | Silyl derivatives of eugenol |
| US5200234A (en) * | 1991-12-16 | 1993-04-06 | Dow Corning Corporation | Method for restoring underground electrical cable |
| US5372840A (en) * | 1993-04-20 | 1994-12-13 | Dow Corning Corporation | Method for enhancing dielectric strength of cable using fluid having a high diffusion coefficient |
| US5372841A (en) * | 1993-04-20 | 1994-12-13 | Dow Corning Corporation | Method for enhancing the dielectrical strength of cable using a fluid mixture |
| US6046156A (en) * | 1998-08-28 | 2000-04-04 | General Electric Company | Fragrance releasing olefinic silanes |
| EP1744866B1 (fr) * | 2004-03-01 | 2012-08-08 | Novinium, Inc. | Procede pour selectionner des formulations pour traiter les cables electriques |
| WO2005084321A2 (fr) * | 2004-03-01 | 2005-09-15 | Novinium, Inc. | Procede pour traiter un cable electrique a pression elevee continue |
| EP1755723B1 (fr) * | 2004-06-04 | 2009-10-21 | Radi Medical Systems Ab | Fil-guide medical avec un capteur |
| EP1897098B1 (fr) * | 2005-04-29 | 2012-05-16 | Dow Corning Corporation | Fluide de restauration de cable electrique |
| US7353601B1 (en) | 2005-08-30 | 2008-04-08 | Novinium, Inc. | Integrated method for restoring electrical power cable |
| AU2007343635B2 (en) * | 2007-01-12 | 2010-10-14 | Utilx Corporation | Composition and method for restoring an electrical cable and inhibiting corrosion in the aluminum conductor core |
| US7700871B2 (en) * | 2007-01-19 | 2010-04-20 | Novinium, Inc. | Acid-catalyzed dielectric enhancement fluid and cable restoration method employing same |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2559342A (en) * | 1949-07-26 | 1951-07-03 | Gen Electric | Organo-silicon compositions |
| US2851471A (en) * | 1954-07-13 | 1958-09-09 | Ethicon Inc | Oxidation of castor oil |
| BE554172A (fr) * | 1956-01-18 | |||
| US3308149A (en) * | 1963-06-13 | 1967-03-07 | Gen Aniline & Film Corp | Organic polyalkyleneoxy silicates |
| DE1543513A1 (de) * | 1965-12-07 | 1969-08-28 | Dynamit Nobel Ag | Verfahren zur Herstellung von halogenierten Phenoxysilanen |
| US3814691A (en) * | 1970-09-25 | 1974-06-04 | Olin Corp | Alkyl(polyalkoxy)silanes as components in hydraulic fluids |
| DE2304503A1 (de) * | 1973-01-31 | 1974-08-01 | Dynamit Nobel Ag | Verfahren zur herstellung von silanestern tertiaerer alkohole |
| US4141851A (en) * | 1975-11-21 | 1979-02-27 | Castrol Limited | Silane derivatives |
| GB1595701A (en) * | 1977-06-24 | 1981-08-19 | Castrol Ltd | Fluids suitable for use as hydraulic fluids electrical oils heat transfer fluids and refrigerant oils |
-
1980
- 1980-12-22 US US06/219,012 patent/US4332957A/en not_active Expired - Fee Related
-
1981
- 1981-11-27 GB GB8135891A patent/GB2090844B/en not_active Expired
- 1981-12-09 FR FR8123049A patent/FR2496667B1/fr not_active Expired
- 1981-12-14 FI FI814005A patent/FI814005L/fi not_active Application Discontinuation
- 1981-12-17 DE DE19813150076 patent/DE3150076A1/de not_active Withdrawn
- 1981-12-18 JP JP56203842A patent/JPS57128695A/ja active Pending
- 1981-12-21 DK DK567781A patent/DK567781A/da not_active Application Discontinuation
- 1981-12-21 LU LU83845A patent/LU83845A1/fr unknown
- 1981-12-21 IT IT25735/81A patent/IT1140373B/it active
- 1981-12-21 NL NL8105755A patent/NL8105755A/nl not_active Application Discontinuation
- 1981-12-21 NO NO814364A patent/NO814364L/no unknown
- 1981-12-21 BR BR8108286A patent/BR8108286A/pt unknown
- 1981-12-22 BE BE0/206911A patent/BE891587A/fr not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| GB2090844A (en) | 1982-07-21 |
| GB2090844B (en) | 1984-09-05 |
| US4332957A (en) | 1982-06-01 |
| FI814005L (fi) | 1982-06-23 |
| NO814364L (no) | 1982-06-23 |
| LU83845A1 (fr) | 1982-07-07 |
| JPS57128695A (en) | 1982-08-10 |
| BR8108286A (pt) | 1982-10-05 |
| FR2496667A1 (fr) | 1982-06-25 |
| IT1140373B (it) | 1986-09-24 |
| IT8125735A0 (it) | 1981-12-21 |
| FR2496667B1 (fr) | 1985-10-11 |
| BE891587A (fr) | 1982-06-22 |
| DK567781A (da) | 1982-06-23 |
| DE3150076A1 (de) | 1982-07-22 |
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