AU708233B2 - Tree resistant cable - Google Patents

Tree resistant cable Download PDF

Info

Publication number: AU708233B2
Authority: AU; Australia
Prior art keywords: range; weight; cable; electrical conductors; parts
Prior art date: 1995-03-30
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.): Ceased

Application number

AU50382/96A

Other languages

English (en)

Other versions

AU5038296A (en

Inventor

Laurence Herbert Gross

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Union Carbide Chemicals and Plastics Technology LLC

Original Assignee

Union Carbide Chemicals and Plastics Technology LLC

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.)

1995-03-30

Filing date

1996-03-29

Publication date

1999-07-29

1996-03-29 Application filed by Union Carbide Chemicals and Plastics Technology LLC filed Critical Union Carbide Chemicals and Plastics Technology LLC

1996-10-10 Publication of AU5038296A publication Critical patent/AU5038296A/en

1999-07-29 Application granted granted Critical

1999-07-29 Publication of AU708233B2 publication Critical patent/AU708233B2/en

2016-03-29 Anticipated expiration legal-status Critical

Status Ceased legal-status Critical Current

Links

-1 each Substances 0.000 claims abstract description 31
239000004698 Polyethylene Substances 0.000 claims abstract description 25
229920000573 polyethylene Polymers 0.000 claims abstract description 25
239000002202 Polyethylene glycol Substances 0.000 claims abstract description 16
229920001223 polyethylene glycol Polymers 0.000 claims abstract description 16
239000000203 mixture Substances 0.000 claims abstract description 14
239000004020 conductor Substances 0.000 claims abstract description 11
229920001577 copolymer Polymers 0.000 claims description 15
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 11
239000005977 Ethylene Substances 0.000 claims description 11
239000000155 melt Substances 0.000 claims description 8
239000004711 α-olefin Substances 0.000 claims description 6
239000003054 catalyst Substances 0.000 claims description 5
125000004432 carbon atom Chemical group C* 0.000 claims description 4
239000004033 plastic Substances 0.000 claims 1
229920003023 plastic Polymers 0.000 claims 1
239000000126 substance Substances 0.000 claims 1
KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 20
TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 10
240000005572 Syzygium cordatum Species 0.000 description 8
235000006650 Syzygium cordatum Nutrition 0.000 description 8
239000011347 resin Substances 0.000 description 8
229920005989 resin Polymers 0.000 description 8
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 4
239000000654 additive Substances 0.000 description 4
NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical group CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 4
239000000463 material Substances 0.000 description 4
239000000243 solution Substances 0.000 description 4
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 description 3
WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 3
239000003963 antioxidant agent Substances 0.000 description 3
239000003431 cross linking reagent Substances 0.000 description 3
239000011810 insulating material Substances 0.000 description 3
238000011144 upstream manufacturing Methods 0.000 description 3
ZNRLMGFXSPUZNR-UHFFFAOYSA-N 2,2,4-trimethyl-1h-quinoline Chemical compound C1=CC=C2C(C)=CC(C)(C)NC2=C1 ZNRLMGFXSPUZNR-UHFFFAOYSA-N 0.000 description 2
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
239000012975 dibutyltin dilaurate Substances 0.000 description 2
150000001993 dienes Chemical class 0.000 description 2
238000001125 extrusion Methods 0.000 description 2
239000000945 filler Substances 0.000 description 2
239000003966 growth inhibitor Substances 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
238000009413 insulation Methods 0.000 description 2
239000012968 metallocene catalyst Substances 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
238000000034 method Methods 0.000 description 2
150000001451 organic peroxides Chemical class 0.000 description 2
150000002978 peroxides Chemical class 0.000 description 2
239000003381 stabilizer Substances 0.000 description 2
RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
DMWVYCCGCQPJEA-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane Chemical compound CC(C)(C)OOC(C)(C)CCC(C)(C)OOC(C)(C)C DMWVYCCGCQPJEA-UHFFFAOYSA-N 0.000 description 1
RPUOOWZETIYCHL-UHFFFAOYSA-N 2-[[2-carboxy-3-(3,5-ditert-butyl-4-hydroxyphenyl)-2-methylpropyl]sulfanylmethyl]-3-(3,5-ditert-butyl-4-hydroxyphenyl)-2-methylpropanoic acid Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CC(C)(CSCC(C)(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(O)=O)C(O)=O)=C1 RPUOOWZETIYCHL-UHFFFAOYSA-N 0.000 description 1
YFHKLSPMRRWLKI-UHFFFAOYSA-N 2-tert-butyl-4-(3-tert-butyl-4-hydroxy-5-methylphenyl)sulfanyl-6-methylphenol Chemical compound CC(C)(C)C1=C(O)C(C)=CC(SC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 YFHKLSPMRRWLKI-UHFFFAOYSA-N 0.000 description 1
HXIQYSLFEXIOAV-UHFFFAOYSA-N 2-tert-butyl-4-(5-tert-butyl-4-hydroxy-2-methylphenyl)sulfanyl-5-methylphenol Chemical compound CC1=CC(O)=C(C(C)(C)C)C=C1SC1=CC(C(C)(C)C)=C(O)C=C1C HXIQYSLFEXIOAV-UHFFFAOYSA-N 0.000 description 1
MQWCQFCZUNBTCM-UHFFFAOYSA-N 2-tert-butyl-6-(3-tert-butyl-2-hydroxy-5-methylphenyl)sulfanyl-4-methylphenol Chemical compound CC(C)(C)C1=CC(C)=CC(SC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O MQWCQFCZUNBTCM-UHFFFAOYSA-N 0.000 description 1
BIISIZOQPWZPPS-UHFFFAOYSA-N 2-tert-butylperoxypropan-2-ylbenzene Chemical compound CC(C)(C)OOC(C)(C)C1=CC=CC=C1 BIISIZOQPWZPPS-UHFFFAOYSA-N 0.000 description 1
XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 description 1
XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical group CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 description 1
239000003508 Dilauryl thiodipropionate Substances 0.000 description 1
239000002656 Distearyl thiodipropionate Substances 0.000 description 1
239000004606 Fillers/Extenders Substances 0.000 description 1
AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
239000006057 Non-nutritive feed additive Substances 0.000 description 1
JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 1
ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
239000006096 absorbing agent Substances 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
SRIDKWFKROYRSX-UHFFFAOYSA-N bis[(2-methylpropan-2-yl)oxy]-phenylphosphane Chemical compound CC(C)(C)OP(OC(C)(C)C)C1=CC=CC=C1 SRIDKWFKROYRSX-UHFFFAOYSA-N 0.000 description 1
239000002981 blocking agent Substances 0.000 description 1
PZGVVCOOWYSSGB-UHFFFAOYSA-L but-2-enedioate;dioctyltin(2+) Chemical compound CCCCCCCC[Sn]1(CCCCCCCC)OC(=O)C=CC(=O)O1 PZGVVCOOWYSSGB-UHFFFAOYSA-L 0.000 description 1
BQAOUQHHGGJEHP-UHFFFAOYSA-N butyl 3-(4-hydroxyphenyl)propanoate Chemical compound CCCCOC(=O)CCC1=CC=C(O)C=C1 BQAOUQHHGGJEHP-UHFFFAOYSA-N 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
238000013329 compounding Methods 0.000 description 1
238000007906 compression Methods 0.000 description 1
230000006835 compression Effects 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
239000007822 coupling agent Substances 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
PNOXNTGLSKTMQO-UHFFFAOYSA-L diacetyloxytin Chemical compound CC(=O)O[Sn]OC(C)=O PNOXNTGLSKTMQO-UHFFFAOYSA-L 0.000 description 1
235000019304 dilauryl thiodipropionate Nutrition 0.000 description 1
235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
239000004205 dimethyl polysiloxane Substances 0.000 description 1
DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 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
230000005684 electric field Effects 0.000 description 1
FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical group CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
238000009533 lab test Methods 0.000 description 1
GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229920001684 low density polyethylene Polymers 0.000 description 1
239000004702 low-density polyethylene Substances 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
238000005259 measurement 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
239000002667 nucleating agent Substances 0.000 description 1
239000003921 oil Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
239000000049 pigment Substances 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
239000012763 reinforcing filler Substances 0.000 description 1
150000004756 silanes Chemical class 0.000 description 1
SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 1
239000012748 slip agent Substances 0.000 description 1
239000000779 smoke Substances 0.000 description 1
125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
LVEOKSIILWWVEO-UHFFFAOYSA-N tetradecyl 3-(3-oxo-3-tetradecoxypropyl)sulfanylpropanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCC LVEOKSIILWWVEO-UHFFFAOYSA-N 0.000 description 1
229910052720 vanadium Inorganic materials 0.000 description 1
LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
UIYCHXAGWOYNNA-UHFFFAOYSA-N vinyl sulfide Chemical group C=CSC=C UIYCHXAGWOYNNA-UHFFFAOYSA-N 0.000 description 1
CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 1

Classifications

- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B7/00—Insulated conductors or cables characterised by their form
- H01B7/17—Protection against damage caused by external factors, e.g. sheaths or armouring
- H01B7/28—Protection against damage caused by moisture, corrosion, chemical attack or weather
- H01B7/2813—Protection against damage caused by electrical, chemical or water tree deterioration
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B7/00—Insulated conductors or cables characterised by their form
- H01B7/17—Protection against damage caused by external factors, e.g. sheaths or armouring
- H01B7/28—Protection against damage caused by moisture, corrosion, chemical attack or weather
- 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

Landscapes

Physics & Mathematics (AREA)
Spectroscopy & Molecular Physics (AREA)
Organic Insulating Materials (AREA)
Compositions Of Macromolecular Compounds (AREA)
Communication Cables (AREA)
Insulated Conductors (AREA)
Flexible Shafts (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

AU50382/96A 1995-03-30 1996-03-29 Tree resistant cable Ceased AU708233B2 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US41323695A	1995-03-30	1995-03-30
US08/413236		1995-03-30

Publications (2)

Publication Number	Publication Date
AU5038296A AU5038296A (en)	1996-10-10
AU708233B2 true AU708233B2 (en)	1999-07-29

Family

ID=23636415

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
AU50382/96A Ceased AU708233B2 (en)	1995-03-30	1996-03-29	Tree resistant cable

Country Status (11)

Country	Link
EP (1)	EP0735545B1 (da)
KR (1)	KR100271686B1 (da)
AT (1)	ATE181453T1 (da)
AU (1)	AU708233B2 (da)
BR (1)	BR9601205A (da)
CA (1)	CA2173038C (da)
DE (1)	DE69602872T2 (da)
DK (1)	DK0735545T3 (da)
ES (1)	ES2135169T3 (da)
GR (1)	GR3030891T3 (da)
TW (1)	TW403916B (da)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5731082A (en) *	1996-06-24	1998-03-24	Union Carbide Chemicals & Plastics Technology Corporation	Tree resistant cable
JPH10168298A (ja) *	1996-12-10	1998-06-23	Elf Atochem Japan Kk	熱可塑性樹脂組成物及び成形品
US5919565A (en) *	1997-03-20	1999-07-06	Union Carbide Chemicals & Plastics Technology Corporation	Tree resistant cable
DK0992041T3 (da) *	1997-06-20	2006-01-16	Union Carbide Chem Plastic	Træresistent kabel
US5962362A (en)	1997-12-09	1999-10-05	Union Carbide Chemicals & Plastics Technology Corporation	Unbridged monocyclopentadienyl metal complex catalyst and a process for polyolefin production
US6127302A (en) *	1997-12-09	2000-10-03	Union Carbide Chemicals & Plastics Technology Corporation	Unbridged monocyclopentadienyl metal complex catalyst and a process for polyolefin production
US6159889A (en) *	1997-12-09	2000-12-12	Union Carbide Chemicals & Plastics Technology Corporation	Unbridged monocyclopentadienyl metal complex catalyst and a process for polyolefin production
US6203907B1 (en) *	1998-04-20	2001-03-20	Union Carbide Chemicals & Plastics Technology Corporation	Tree resistant cable
TWI224607B (en)	1998-06-16	2004-12-01	Union Carbide Chem Plastic	Tree resistant cable
EP0989139A1 (en) *	1998-09-25	2000-03-29	Union Carbide Chemicals & Plastics Technology Corporation	Unbridged monocyclopentadienyl metal complex catalyst for olefin polymerization by reacting with particulate solids with functional groups
MXPA01005017A (es) *	1998-11-20	2003-09-10	Union Carbide Chem Plastic	Un proceso para controlar ramificaciones de agua.
SE516260C2 (sv) *	1999-07-01	2001-12-10	Borealis Polymers Oy	Isolerande komposition för en elektrisk kraftkabel
US6191230B1 (en) *	1999-07-22	2001-02-20	Union Carbide Chemicals & Plastics Technology Corporation	Polyethylene crosslinkable composition
EP1564261B1 (de)	2004-02-09	2016-05-25	Merck Patent GmbH	Interferenzpigmente
KR102210037B1 (ko)	2012-12-21	2021-02-01	다우 글로벌 테크놀로지스 엘엘씨	개선된 발포성 및 향상된 가공성을 위한 폴리올레핀-기재 케이블 화합물 제제
WO2019178747A1 (en)	2018-03-20	2019-09-26	Dow Global Technologies Llc	Polyolefin-and-polyvinylpyrrolidone formulation

Citations (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4305849A (en) *	1979-08-16	1981-12-15	Nippon Unicar Company Limited	Polyolefin composition containing high molecular weight polyethylene glycol useful for electrical insulation
US4812505A (en) *	1987-05-18	1989-03-14	Union Carbide Corporation	Tree resistant compositions
US5246783A (en) *	1991-08-15	1993-09-21	Exxon Chemical Patents Inc.	Electrical devices comprising polymeric insulating or semiconducting members

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS57126004A (en) *	1981-01-30	1982-08-05	Nippon Unicar Co Ltd	Semiconductive polyolefin composition and cable using same
CA1181940A (en) *	1982-03-31	1985-02-05	Robert J. Turbett	Compositions of hydrocarbon-substituted diphenyl amines and high molecular weight polyethylene glycols; and the use thereof as water-tree retardants for polymers
JPS63310517A (ja) *	1987-06-11	1988-12-19	Sanyo Electric Co Ltd	超伝導線材化法

1996
- 1996-03-07 TW TW085102785A patent/TW403916B/zh not_active IP Right Cessation
- 1996-03-15 EP EP96301806A patent/EP0735545B1/en not_active Expired - Lifetime
- 1996-03-15 AT AT96301806T patent/ATE181453T1/de not_active IP Right Cessation
- 1996-03-15 ES ES96301806T patent/ES2135169T3/es not_active Expired - Lifetime
- 1996-03-15 DE DE69602872T patent/DE69602872T2/de not_active Expired - Lifetime
- 1996-03-15 DK DK96301806T patent/DK0735545T3/da active
- 1996-03-26 KR KR1019960008291A patent/KR100271686B1/ko not_active Expired - Lifetime
- 1996-03-29 AU AU50382/96A patent/AU708233B2/en not_active Ceased
- 1996-03-29 BR BR9601205A patent/BR9601205A/pt not_active IP Right Cessation
- 1996-03-29 CA CA002173038A patent/CA2173038C/en not_active Expired - Lifetime
1999
- 1999-07-30 GR GR990401972T patent/GR3030891T3/el unknown

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4305849A (en) *	1979-08-16	1981-12-15	Nippon Unicar Company Limited	Polyolefin composition containing high molecular weight polyethylene glycol useful for electrical insulation
US4812505A (en) *	1987-05-18	1989-03-14	Union Carbide Corporation	Tree resistant compositions
US5246783A (en) *	1991-08-15	1993-09-21	Exxon Chemical Patents Inc.	Electrical devices comprising polymeric insulating or semiconducting members

Also Published As

Publication number	Publication date
TW403916B (en)	2000-09-01
CA2173038C (en)	1999-08-10
AU5038296A (en)	1996-10-10
EP0735545A2 (en)	1996-10-02
GR3030891T3 (en)	1999-11-30
CA2173038A1 (en)	1996-10-01
DK0735545T3 (da)	1999-11-22
DE69602872T2 (de)	1999-10-21
ATE181453T1 (de)	1999-07-15
BR9601205A (pt)	1998-01-06
EP0735545B1 (en)	1999-06-16
KR960035666A (ko)	1996-10-24
ES2135169T3 (es)	1999-10-16
EP0735545A3 (en)	1997-04-16
DE69602872D1 (de)	1999-07-22
KR100271686B1 (ko)	2000-11-15

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Date	Code	Title	Description
2003-10-30	MK14	Patent ceased section 143(a) (annual fees not paid) or expired

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