GB1200739A - Method of improving dielectrics - Google Patents
Method of improving dielectricsInfo
- Publication number
- GB1200739A GB1200739A GB26120/67A GB2612067A GB1200739A GB 1200739 A GB1200739 A GB 1200739A GB 26120/67 A GB26120/67 A GB 26120/67A GB 2612067 A GB2612067 A GB 2612067A GB 1200739 A GB1200739 A GB 1200739A
- Authority
- GB
- United Kingdom
- Prior art keywords
- triphenyl
- antimony
- tin
- polyethylene
- dicyclopentadienyl
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 239000003989 dielectric material Substances 0.000 title 1
- -1 vinylidene halides Chemical class 0.000 abstract 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 abstract 4
- 239000004698 Polyethylene Substances 0.000 abstract 3
- 229910052742 iron Inorganic materials 0.000 abstract 3
- 229920000573 polyethylene Polymers 0.000 abstract 3
- 229920000642 polymer Polymers 0.000 abstract 3
- YDDDHSUYUDHYCR-UHFFFAOYSA-N C(C)(=O)[Fe](C1C=CC=C1)C1C=CC=C1 Chemical compound C(C)(=O)[Fe](C1C=CC=C1)C1C=CC=C1 YDDDHSUYUDHYCR-UHFFFAOYSA-N 0.000 abstract 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 2
- 239000004642 Polyimide Substances 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 abstract 2
- 229910052787 antimony Inorganic materials 0.000 abstract 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 abstract 2
- 229920002301 cellulose acetate Polymers 0.000 abstract 2
- 229920001577 copolymer Polymers 0.000 abstract 2
- 239000003822 epoxy resin Substances 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 150000002894 organic compounds Chemical class 0.000 abstract 2
- 229920000058 polyacrylate Polymers 0.000 abstract 2
- 229920000647 polyepoxide Polymers 0.000 abstract 2
- 229920000570 polyether Polymers 0.000 abstract 2
- 229920001721 polyimide Polymers 0.000 abstract 2
- 229920001021 polysulfide Polymers 0.000 abstract 2
- 229920002635 polyurethane Polymers 0.000 abstract 2
- 239000004814 polyurethane Substances 0.000 abstract 2
- BPLUKJNHPBNVQL-UHFFFAOYSA-N triphenylarsine Chemical compound C1=CC=CC=C1[As](C=1C=CC=CC=1)C1=CC=CC=C1 BPLUKJNHPBNVQL-UHFFFAOYSA-N 0.000 abstract 2
- ZHXAZZQXWJJBHA-UHFFFAOYSA-N triphenylbismuthane Chemical compound C1=CC=CC=C1[Bi](C=1C=CC=CC=1)C1=CC=CC=C1 ZHXAZZQXWJJBHA-UHFFFAOYSA-N 0.000 abstract 2
- AKQNYQDSIDKVJZ-UHFFFAOYSA-N triphenylsilane Chemical compound C1=CC=CC=C1[SiH](C=1C=CC=CC=1)C1=CC=CC=C1 AKQNYQDSIDKVJZ-UHFFFAOYSA-N 0.000 abstract 2
- HVYVMSPIJIWUNA-UHFFFAOYSA-N triphenylstibine Chemical compound C1=CC=CC=C1[Sb](C=1C=CC=CC=1)C1=CC=CC=C1 HVYVMSPIJIWUNA-UHFFFAOYSA-N 0.000 abstract 2
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 abstract 1
- VLDPXPPHXDGHEW-UHFFFAOYSA-N 1-chloro-2-dichlorophosphoryloxybenzene Chemical compound ClC1=CC=CC=C1OP(Cl)(Cl)=O VLDPXPPHXDGHEW-UHFFFAOYSA-N 0.000 abstract 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract 1
- 239000005062 Polybutadiene Substances 0.000 abstract 1
- 229920002367 Polyisobutene Polymers 0.000 abstract 1
- 239000004721 Polyphenylene oxide Substances 0.000 abstract 1
- 239000004743 Polypropylene Substances 0.000 abstract 1
- 239000004793 Polystyrene Substances 0.000 abstract 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- 150000001336 alkenes Chemical class 0.000 abstract 1
- 229910052785 arsenic Inorganic materials 0.000 abstract 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 abstract 1
- 229910052797 bismuth Inorganic materials 0.000 abstract 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 abstract 1
- 239000004020 conductor Substances 0.000 abstract 1
- JJPZOIJCDNHCJP-UHFFFAOYSA-N dibutyl(sulfanylidene)tin Chemical compound CCCC[Sn](=S)CCCC JJPZOIJCDNHCJP-UHFFFAOYSA-N 0.000 abstract 1
- 150000001993 dienes Chemical class 0.000 abstract 1
- RIBJLXBLWQKWLO-UHFFFAOYSA-N diphenylstiborylbenzene Chemical compound C=1C=CC=CC=1[Sb](C=1C=CC=CC=1)(=O)C1=CC=CC=C1 RIBJLXBLWQKWLO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052732 germanium Inorganic materials 0.000 abstract 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 abstract 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 abstract 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 abstract 1
- 238000009413 insulation Methods 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- PQEAVIKJSKOOHN-UHFFFAOYSA-N methyl 2-amino-3-(1-methylimidazol-4-yl)propanoate Chemical compound COC(=O)C(N)CC1=CN(C)C=N1 PQEAVIKJSKOOHN-UHFFFAOYSA-N 0.000 abstract 1
- 238000005065 mining Methods 0.000 abstract 1
- 229910052759 nickel Inorganic materials 0.000 abstract 1
- 229920000620 organic polymer Polymers 0.000 abstract 1
- 230000000737 periodic effect Effects 0.000 abstract 1
- 229910052698 phosphorus Inorganic materials 0.000 abstract 1
- 239000011574 phosphorus Substances 0.000 abstract 1
- 229920001084 poly(chloroprene) Polymers 0.000 abstract 1
- 229920002239 polyacrylonitrile Polymers 0.000 abstract 1
- 229920002857 polybutadiene Polymers 0.000 abstract 1
- 229920000515 polycarbonate Polymers 0.000 abstract 1
- 239000004417 polycarbonate Substances 0.000 abstract 1
- 229920000728 polyester Polymers 0.000 abstract 1
- 229920000139 polyethylene terephthalate Polymers 0.000 abstract 1
- 239000005020 polyethylene terephthalate Substances 0.000 abstract 1
- 229920001195 polyisoprene Polymers 0.000 abstract 1
- 229920001155 polypropylene Polymers 0.000 abstract 1
- 229920002223 polystyrene Polymers 0.000 abstract 1
- FZHCFNGSGGGXEH-UHFFFAOYSA-N ruthenocene Chemical compound [Ru+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 FZHCFNGSGGGXEH-UHFFFAOYSA-N 0.000 abstract 1
- 229910052710 silicon Inorganic materials 0.000 abstract 1
- 239000010703 silicon Substances 0.000 abstract 1
- 229920003048 styrene butadiene rubber Polymers 0.000 abstract 1
- 229920001897 terpolymer Polymers 0.000 abstract 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 abstract 1
- CRHIAMBJMSSNNM-UHFFFAOYSA-N tetraphenylstannane Chemical compound C1=CC=CC=C1[Sn](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 CRHIAMBJMSSNNM-UHFFFAOYSA-N 0.000 abstract 1
- 229910052718 tin Inorganic materials 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/303—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups H01B3/38 or H01B3/302
- H01B3/306—Polyimides or polyesterimides
-
- 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
- C08K5/56—Organo-metallic compounds, i.e. organic compounds containing a metal-to-carbon bond
-
- 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
- C08K5/56—Organo-metallic compounds, i.e. organic compounds containing a metal-to-carbon bond
- C08K5/57—Organo-tin compounds
-
- 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
- C08K5/56—Organo-metallic compounds, i.e. organic compounds containing a metal-to-carbon bond
- C08K5/57—Organo-tin compounds
- C08K5/58—Organo-tin compounds containing sulfur
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Insulating Materials (AREA)
- Epoxy Resins (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
Abstract
1,200,739. Polymer compositions. MINNESOTA MINING & MFG. CO. 6 June, 1967 [7 June, 1966], No. 26120/67. Headings C3B, C3F, C3P and C3R. [Also in Division C7] Insulation for electrical conductors suitable for high voltages comprises a dielectric organic polymer and 0À1 to 20% by weight of the polymer of an organo compound of an element of Groups IVB, VB or VIII of the Periodic Table of Elements having an atomic number of 14 to 83. Many polymeric materials are specified including epoxy resins; cellulose acetate; polymers of olefins, diolefins, vinyl and vinylidene halides, tetrafluoroethylene, hexafluoropropylene, styrene and acrylic compounds; polyurethanes; polysulphides; polyesters; polycarbonates; polyimides and chlorinated polyethers. Organo compounds of silicon, germanium, tin, lead, phosphorus, arsenic, antimony, bismuth and iron are listed, and examples describe compositions of (1) polyacrylate and triphenyl silane, polyacrylonitrile and trinaphthyl antimony, polyurethane and dioyclopentadienyl nickel, polychloroprene and triphenyl arsenic, polyisobutylene and triphenyl bismuth, polyisoprene and acetyl dicyclopentadienyl iron, chlorosulphonated polyethylene and dibutyl tin sulphide, ethylene/propylene copolymer and triphenyl lead chloride, polybutadiene and dicyclopentadienyl iron, styrene/butadiene copolymer and dicyclopentadienyl ruthenium, polysulphide and bis(tributyl tin) oxide, and vinylidene fluoride/ hexafluoropropene copolymer and triphenyl phosphine; (2) polyethylene and triphenyl arsenic, polyacrylate and triphenyl silane, ABS terpolymer and bis(tributyl tin) oxide, cellulose acetate and triphenyl antimony oxide, polystyrene and triphenyl antimony, and chlorinated polyether and acetyl dicyclopentadienyl iron; (3) polyethylene terephthalate and tetraphenyl tin; (4) polypropylene and triphenyl bismuth; (5) epoxy resin and dicyclopentadienyl iron; (6) polyimide derived from pyromellitic dianhydride and 4,4<SP>1</SP>-diaminodiphenyl ether and triphenyl phosphine; and (7) polyethylene and triphenyl antimony.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US55569566A | 1966-06-07 | 1966-06-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1200739A true GB1200739A (en) | 1970-07-29 |
Family
ID=24218261
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB26120/67A Expired GB1200739A (en) | 1966-06-07 | 1967-06-06 | Method of improving dielectrics |
Country Status (3)
| Country | Link |
|---|---|
| JP (1) | JPS4519663B1 (en) |
| DE (1) | DE1694623B2 (en) |
| GB (1) | GB1200739A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4049618A (en) | 1972-02-17 | 1977-09-20 | Syntex (U.S.A.) Inc. | Polyvinyl chloride composition containing ferrocene smoke suppressant additives |
| US4076657A (en) * | 1974-07-05 | 1978-02-28 | Syntex (U.S.A.) Inc. | Polyurethane smoke suppression additive |
| WO1993014157A1 (en) * | 1992-01-17 | 1993-07-22 | E.I. Du Pont De Nemours And Company | Process for preparing a strengthened polyimide film containing organometallic compounds for improving adhesion |
| EP3070115A1 (en) * | 2015-03-19 | 2016-09-21 | ABB Research Ltd. | Epoxy resin composition with improved dielectric breakdown strength |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5957313B2 (en) * | 2012-06-27 | 2016-07-27 | 住友化学株式会社 | Film containing organic antimony compound and polymer compound |
-
1967
- 1967-05-10 JP JP2919167A patent/JPS4519663B1/ja active Pending
- 1967-06-06 DE DE19671694623 patent/DE1694623B2/en active Pending
- 1967-06-06 GB GB26120/67A patent/GB1200739A/en not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4049618A (en) | 1972-02-17 | 1977-09-20 | Syntex (U.S.A.) Inc. | Polyvinyl chloride composition containing ferrocene smoke suppressant additives |
| US4076657A (en) * | 1974-07-05 | 1978-02-28 | Syntex (U.S.A.) Inc. | Polyurethane smoke suppression additive |
| WO1993014157A1 (en) * | 1992-01-17 | 1993-07-22 | E.I. Du Pont De Nemours And Company | Process for preparing a strengthened polyimide film containing organometallic compounds for improving adhesion |
| US5272194A (en) * | 1992-01-17 | 1993-12-21 | E. I. Du Pont De Nemours And Company | Process for preparing a strengthened polyimide film containing organometallic compounds for improving adhesion |
| EP3070115A1 (en) * | 2015-03-19 | 2016-09-21 | ABB Research Ltd. | Epoxy resin composition with improved dielectric breakdown strength |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS4519663B1 (en) | 1970-07-04 |
| DE1694623A1 (en) | 1970-11-05 |
| DE1694623B2 (en) | 1972-04-20 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |