NO784363L - Isolert traad eller kabel. - Google Patents

Isolert traad eller kabel.

Info

Publication number: NO784363L
Authority: NO; Norway
Prior art keywords: water; substituted; ethylene; cable; electric wire
Prior art date: 1977-12-27

Application number

NO784363A

Other languages

English (en)

Norwegian (no)

Inventor

Arnold Clifton Ashcraft

Robert John Turbett

Timothy Richard Burke

Original Assignee

Union Carbide Corp

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.)

1977-12-27

Filing date

1978-12-22

Publication date

1979-06-28

1978-12-22 Application filed by Union Carbide Corp filed Critical Union Carbide Corp

1979-06-28 Publication of NO784363L publication Critical patent/NO784363L/no

Links

239000000203 mixture Substances 0.000 claims description 48
229920000573 polyethylene Polymers 0.000 claims description 23
238000000034 method Methods 0.000 claims description 15
150000001282 organosilanes Chemical class 0.000 claims description 13
238000009413 insulation Methods 0.000 claims description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
239000003431 cross linking reagent Substances 0.000 claims description 9
239000003112 inhibitor Substances 0.000 claims description 9
229920001577 copolymer Polymers 0.000 claims description 7
XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 claims description 6
125000004104 aryloxy group Chemical group 0.000 claims description 6
239000004020 conductor Substances 0.000 claims description 4
229920000089 Cyclic olefin copolymer Polymers 0.000 claims description 3
150000001336 alkenes Chemical class 0.000 claims description 3
125000003118 aryl group Chemical group 0.000 claims description 3
125000000732 arylene group Chemical group 0.000 claims description 3
238000004132 cross linking Methods 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 3
150000001451 organic peroxides Chemical class 0.000 claims description 3
239000004711 α-olefin Substances 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
125000000217 alkyl group Chemical group 0.000 claims 2
125000004423 acyloxy group Chemical group 0.000 claims 1
125000003545 alkoxy group Chemical group 0.000 claims 1
125000002947 alkylene group Chemical group 0.000 claims 1
240000005572 Syzygium cordatum Species 0.000 description 17
235000006650 Syzygium cordatum Nutrition 0.000 description 17
-1 polyethylene Polymers 0.000 description 13
239000003989 dielectric material Substances 0.000 description 11
239000005977 Ethylene Substances 0.000 description 10
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 9
230000015556 catabolic process Effects 0.000 description 9
238000012360 testing method Methods 0.000 description 8
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 7
239000004698 Polyethylene Substances 0.000 description 7
239000000654 additive Substances 0.000 description 7
239000003963 antioxidant agent Substances 0.000 description 7
229920000642 polymer Polymers 0.000 description 7
230000015572 biosynthetic process Effects 0.000 description 6
150000001875 compounds Chemical class 0.000 description 6
239000000155 melt Substances 0.000 description 6
230000003078 antioxidant effect Effects 0.000 description 4
230000000694 effects Effects 0.000 description 4
230000005684 electric field Effects 0.000 description 4
229920001684 low density polyethylene Polymers 0.000 description 4
239000004702 low-density polyethylene Substances 0.000 description 4
229920001169 thermoplastic Polymers 0.000 description 4
239000004416 thermosoftening plastic Substances 0.000 description 4
239000008151 electrolyte solution Substances 0.000 description 3
239000011810 insulating material Substances 0.000 description 3
150000002978 peroxides Chemical group 0.000 description 3
229920005638 polyethylene monopolymer Polymers 0.000 description 3
239000000047 product Substances 0.000 description 3
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
239000007787 solid Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
239000002023 wood Substances 0.000 description 3
XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 description 2
TXFPEBPIARQUIG-UHFFFAOYSA-N 4'-hydroxyacetophenone Chemical compound CC(=O)C1=CC=C(O)C=C1 TXFPEBPIARQUIG-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
230000000996 additive effect Effects 0.000 description 2
ASCHNMXUWBEZDM-UHFFFAOYSA-N chloridodioxygen(.) Chemical compound [O]OCl ASCHNMXUWBEZDM-UHFFFAOYSA-N 0.000 description 2
238000011109 contamination Methods 0.000 description 2
238000000354 decomposition reaction Methods 0.000 description 2
238000010586 diagram Methods 0.000 description 2
239000012153 distilled water Substances 0.000 description 2
229920001971 elastomer Polymers 0.000 description 2
239000003792 electrolyte Substances 0.000 description 2
229920001038 ethylene copolymer Polymers 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
229920001519 homopolymer Polymers 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
238000005259 measurement Methods 0.000 description 2
229920000098 polyolefin Polymers 0.000 description 2
238000012545 processing Methods 0.000 description 2
229910000077 silane Inorganic materials 0.000 description 2
238000010998 test method Methods 0.000 description 2
QYCGBAJADAGLLK-UHFFFAOYSA-N 1-(cyclohepten-1-yl)cycloheptene Chemical compound C1CCCCC=C1C1=CCCCCC1 QYCGBAJADAGLLK-UHFFFAOYSA-N 0.000 description 1
KAJRUHJCBCZULP-UHFFFAOYSA-N 1-cyclohepta-1,3-dien-1-ylcyclohepta-1,3-diene Chemical compound C1CCC=CC=C1C1=CC=CCCC1 KAJRUHJCBCZULP-UHFFFAOYSA-N 0.000 description 1
KSNRDYQOHXQKAB-UHFFFAOYSA-N 2,2,4-trimethyl-3,4-dihydro-1h-quinoline Chemical compound C1=CC=C2C(C)CC(C)(C)NC2=C1 KSNRDYQOHXQKAB-UHFFFAOYSA-N 0.000 description 1
RBTBFTRPCNLSDE-UHFFFAOYSA-N 3,7-bis(dimethylamino)phenothiazin-5-ium Chemical compound C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 RBTBFTRPCNLSDE-UHFFFAOYSA-N 0.000 description 1
XOUQAVYLRNOXDO-UHFFFAOYSA-N 6-tert-butyl-m-cresol Natural products CC1=CC=C(C(C)(C)C)C(O)=C1 XOUQAVYLRNOXDO-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
201000004624 Dermatitis Diseases 0.000 description 1
206010013142 Disinhibition Diseases 0.000 description 1
239000002656 Distearyl thiodipropionate Substances 0.000 description 1
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
229920000181 Ethylene propylene rubber Polymers 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
244000043261 Hevea brasiliensis Species 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
229920006311 Urethane elastomer Polymers 0.000 description 1
230000001133 acceleration Effects 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
208000010668 atopic eczema Diseases 0.000 description 1
238000009835 boiling Methods 0.000 description 1
IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
238000010382 chemical cross-linking Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
229910000423 chromium oxide Inorganic materials 0.000 description 1
230000003750 conditioning effect Effects 0.000 description 1
239000000356 contaminant Substances 0.000 description 1
230000002950 deficient Effects 0.000 description 1
150000001993 dienes Chemical class 0.000 description 1
PWWSSIYVTQUJQQ-UHFFFAOYSA-N distearyl thiodipropionate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCCCCCC PWWSSIYVTQUJQQ-UHFFFAOYSA-N 0.000 description 1
235000019305 distearyl thiodipropionate Nutrition 0.000 description 1
239000000975 dye Substances 0.000 description 1
239000000806 elastomer Substances 0.000 description 1
CGPRUXZTHGTMKW-UHFFFAOYSA-N ethene;ethyl prop-2-enoate Chemical compound C=C.CCOC(=O)C=C CGPRUXZTHGTMKW-UHFFFAOYSA-N 0.000 description 1
HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
229920001903 high density polyethylene Polymers 0.000 description 1
239000004700 high-density polyethylene Substances 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
239000012774 insulation material Substances 0.000 description 1
230000016507 interphase Effects 0.000 description 1
238000011835 investigation Methods 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
230000007774 longterm Effects 0.000 description 1
239000010687 lubricating oil Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
239000006078 metal deactivator Substances 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
229960000907 methylthioninium chloride Drugs 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229920003052 natural elastomer Polymers 0.000 description 1
229920001194 natural rubber Polymers 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
230000002028 premature Effects 0.000 description 1
238000011160 research Methods 0.000 description 1
239000004065 semiconductor Substances 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
229920000468 styrene butadiene styrene block copolymer Polymers 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000012815 thermoplastic material Substances 0.000 description 1
239000010936 titanium Substances 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
238000012546 transfer Methods 0.000 description 1
238000009489 vacuum treatment Methods 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
UIYCHXAGWOYNNA-UHFFFAOYSA-N vinyl sulfide Chemical group C=CSC=C UIYCHXAGWOYNNA-UHFFFAOYSA-N 0.000 description 1
238000004073 vulcanization Methods 0.000 description 1
230000003313 weakening effect Effects 0.000 description 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
- H01B3/44—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 vinyl resins; acrylic resins
- H01B3/441—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 vinyl resins; acrylic resins from alkenes
- 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
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
- 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
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
- C08F255/02—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having two or three carbon atoms
- 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
- C08K5/5425—Silicon-containing compounds containing oxygen containing at least one C=C bond

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Physics & Mathematics (AREA)
Spectroscopy & Molecular Physics (AREA)
Organic Insulating Materials (AREA)
Compositions Of Macromolecular Compounds (AREA)
Insulated Conductors (AREA)
Communication Cables (AREA)

NO784363A 1977-12-27 1978-12-22 Isolert traad eller kabel. NO784363L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US86475177A	1977-12-27	1977-12-27

Publications (1)

Publication Number	Publication Date
NO784363L true NO784363L (no)	1979-06-28

Family

ID=25343986

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO784363A NO784363L (no)	1977-12-27	1978-12-22	Isolert traad eller kabel.

Country Status (10)

Country	Link
EP (1)	EP0002830B1 (da)
JP (1)	JPS54129382A (da)
AR (1)	AR224866A1 (da)
AU (1)	AU524306B2 (da)
BR (1)	BR7808478A (da)
CA (1)	CA1103915A (da)
DE (1)	DE2862277D1 (da)
DK (1)	DK579478A (da)
NO (1)	NO784363L (da)
ZA (1)	ZA787062B (da)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AT374298B (de) *	1979-07-26	1984-04-10	Union Carbide Corp	Isolierstoffmischung, insbesondere als isolierung elektrischer draehte oder kabel
DE2935224A1 (de) *	1979-08-31	1981-03-19	Kabel- und Metallwerke Gutehoffnungshütte AG, 3000 Hannover	Wasserfeste hochspannungsisolierung fuer elektrische kabel
US4369331A (en) *	1980-12-22	1983-01-18	Union Carbide Corporation	Ethylene polymer compositions stabilized against water treeing by an organic titanate; and the use thereof as insulation about electrical conductors
US4376180A (en) *	1981-09-30	1983-03-08	Union Carbide Corporation	Ethylene polymers stabilized against water-treeing by N-phenyl substituted amino silanes; and the use of these compositions as insulation about electrical conductors
WO1983001893A1 (en) *	1981-12-01	1983-06-09	Univ California	A catheter assembly
EP0109797A3 (en) *	1982-11-18	1984-06-27	Dow Corning Corporation	Polymeric compositions resistant to electrical and water treeing
EP0114495A3 (en) *	1982-12-27	1984-10-17	Dow Corning Corporation	Anti-treeing additives
US4514539A (en) *	1983-05-05	1985-04-30	Reichhold Chemicals, Inc.	Stain resistant polymeric insulating compositions
JPS60167206A (ja) *	1984-02-09	1985-08-30	株式会社フジクラ	直流電力ケ−ブル用絶縁体組成物およびこれを用いた直流電力ケ−ブル
IT1186155B (it) *	1985-12-20	1987-11-18	Pirelli Cavi Spa	Cavi elettrici e materiale per formare rivestimenti di conduttori di cavi elettrici
CA1284405C (en) *	1986-01-13	1991-05-28	Dow Corning Corporation	Mineral filled rubber composites
US4840983A (en) *	1986-05-23	1989-06-20	Dow Corning Corporation	Anti-treeing additives
KR100345419B1 (ko) *	1994-04-20	2002-11-29	더 다우 케미칼 캄파니	실질적으로선형인실란가교결합성에틸렌중합체,이의제조방법및이로부터제조된제품
US5824718A (en) *	1995-04-20	1998-10-20	The Dow Chemical Company	Silane-crosslinkable, substantially linear ethylene polymers and their uses
CN116444727B (zh) *	2022-01-06	2026-02-06	中国石油化工股份有限公司	抗水树改性丙烯基热塑性绝缘材料及其制备方法和应用
CN116444931B (zh) *	2022-01-06	2025-12-09	中国石油化工股份有限公司	耐电树枝化热塑性绝缘材料及其制备方法和应用

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3079370A (en)	1955-05-18	1963-02-26	Gen Electric	Peroxide cured polyethylene
CA647433A (en)	1955-05-18	1962-08-28	General Electric Company	Peroxide cured polyethylene
BE547998A (da)	1955-05-24
NL126833C (da)	1959-01-14
US3296189A (en)	1965-07-29	1967-01-03	Warren O Eastman	Chemically cross-linked polyethylene stabilized with polymerized trimethyl quinoline
DE1694612A1 (de) *	1966-04-13	1970-09-17	Monsanto Co	Verstaerkte Polyolefine und Verfahren zur Herstellung derselben
BE794718Q (fr) *	1968-12-20	1973-05-16	Dow Corning Ltd	Procede de reticulation d'olefines
US3606736A (en)	1969-06-16	1971-09-21	Wheelabrator Corp	Apparatus for filtering suspended solids from gaseous medium and for removal of filter cake from filter elements
GB1346588A (en) *	1970-10-14	1974-02-13	Dow Corning Ltd	Cross linked polyolefin sheets and films and the preparation thereof
BE794485A (fr) *	1972-02-04	1973-05-16	Gen Electric	Acryloxy et methacryloxy silanes et procede de fabrication
US3922442A (en) *	1972-06-01	1975-11-25	Nat Distillers Chem Corp	Flame retardant compositions
JPS565257B2 (da) *	1973-07-16	1981-02-04
US3957719A (en) *	1974-08-08	1976-05-18	General Electric Company	Method of heat treating an ethylene containing polymer electrical insulating composition and product formed thereby
JPS5134866A (ja) *	1974-09-19	1976-03-24	Asahi Chemical Ind	Haigasujokahoho
US4011382A (en)	1975-03-10	1977-03-08	Union Carbide Corporation	Preparation of low and medium density ethylene polymer in fluid bed reactor
GB1502164A (en) *	1976-02-20	1978-02-22	Ici Ltd	Organo-silicon compounds and their use for cross-linking polymers
FR2353119A1 (fr) *	1976-05-25	1977-12-23	Comp Generale Electricite	Cable electrique de puissance resistant a l'humidite
US4133789A (en) *	1977-11-03	1979-01-09	Gulf Oil Corporation	Adhesive composition for bonding a low-energy plastic surface to metal
ZA787061B (en) *	1977-12-27	1980-08-27	Union Carbide Corp	Dielectric compositions stabilized against water treeing with organo silane compounds
NZ190052A (en) *	1978-03-31	1980-11-14	Union Carbide Corp	Water-curable silane-modified alkylene alkylacrylate copolymers

1978
- 1978-12-18 ZA ZA787062A patent/ZA787062B/xx unknown
- 1978-12-21 CA CA318,390A patent/CA1103915A/en not_active Expired
- 1978-12-21 AU AU42812/78A patent/AU524306B2/en not_active Expired
- 1978-12-22 NO NO784363A patent/NO784363L/no unknown
- 1978-12-22 DK DK579478A patent/DK579478A/da unknown
- 1978-12-26 JP JP15938878A patent/JPS54129382A/ja active Granted
- 1978-12-26 AR AR274965A patent/AR224866A1/es active
- 1978-12-26 BR BR7808478A patent/BR7808478A/pt unknown
- 1978-12-27 DE DE7878101852T patent/DE2862277D1/de not_active Expired
- 1978-12-27 EP EP78101852A patent/EP0002830B1/en not_active Expired

Also Published As

Publication number	Publication date
CA1103915A (en)	1981-06-30
ZA787062B (en)	1980-04-30
AR224866A1 (es)	1982-01-29
AU4281278A (en)	1979-07-05
JPS5757804B2 (da)	1982-12-07
EP0002830A2 (en)	1979-07-11
BR7808478A (pt)	1979-07-31
DK579478A (da)	1979-06-28
AU524306B2 (en)	1982-09-09
EP0002830B1 (en)	1983-05-25
DE2862277D1 (en)	1983-07-07
EP0002830A3 (en)	1979-07-25
JPS54129382A (en)	1979-10-06

Publication	Publication Date	Title
NO784362L (no)	1979-06-28	Dielektrisk preparat.
NO784363L (no)	1979-06-28	Isolert traad eller kabel.
US4212756A (en)	1980-07-15	Dielectric composition stabilized against water treeing with organo silane compounds
KR880002101B1 (ko)	1988-10-15	반도체 폴리올레핀 조성물 및 이 조성물로 피복된 케이블
KR100413016B1 (ko)	2003-12-31	트리 내성 케이블
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