JPS58201843A - ウォータートリーイング抵抗性を有するエチレン系重合体組成物 - Google Patents
ウォータートリーイング抵抗性を有するエチレン系重合体組成物Info
- Publication number
- JPS58201843A JPS58201843A JP58052821A JP5282183A JPS58201843A JP S58201843 A JPS58201843 A JP S58201843A JP 58052821 A JP58052821 A JP 58052821A JP 5282183 A JP5282183 A JP 5282183A JP S58201843 A JPS58201843 A JP S58201843A
- Authority
- JP
- Japan
- Prior art keywords
- composition according
- composition
- water
- diphenylamine
- hydrocarbon
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims description 73
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 title claims description 61
- 240000005572 Syzygium cordatum Species 0.000 title claims description 35
- 235000006650 Syzygium cordatum Nutrition 0.000 title claims description 35
- 229920001223 polyethylene glycol Polymers 0.000 title claims description 24
- 229920000642 polymer Polymers 0.000 title claims description 16
- 239000002202 Polyethylene glycol Substances 0.000 title claims description 11
- 239000004215 Carbon black (E152) Substances 0.000 title claims description 7
- 229930195733 hydrocarbon Natural products 0.000 title claims description 7
- 239000003112 inhibitor Substances 0.000 title description 6
- 125000001183 hydrocarbyl group Chemical group 0.000 title 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 28
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 19
- 229910000077 silane Inorganic materials 0.000 claims description 19
- 229920000573 polyethylene Polymers 0.000 claims description 13
- 239000004705 High-molecular-weight polyethylene Chemical class 0.000 claims description 10
- -1 methylvinylsiloxane Chemical class 0.000 claims description 10
- 239000000654 additive Substances 0.000 claims description 9
- 238000004132 cross linking Methods 0.000 claims description 9
- 239000003623 enhancer Substances 0.000 claims description 9
- 150000002430 hydrocarbons Chemical group 0.000 claims description 9
- 239000007788 liquid Substances 0.000 claims description 9
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 8
- 230000000996 additive effect Effects 0.000 claims description 8
- 150000001412 amines Chemical class 0.000 claims description 8
- 229920001577 copolymer Polymers 0.000 claims description 8
- 150000001451 organic peroxides Chemical class 0.000 claims description 8
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical group CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 claims description 5
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims description 4
- 239000004698 Polyethylene Substances 0.000 claims description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 8
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 4
- 230000002401 inhibitory effect Effects 0.000 claims 3
- MJXSSIDXOOAJHN-UHFFFAOYSA-N 1,2-dihydroxyethanesulfonic acid Chemical class OCC(O)S(O)(=O)=O MJXSSIDXOOAJHN-UHFFFAOYSA-N 0.000 claims 1
- 229920001038 ethylene copolymer Polymers 0.000 claims 1
- 238000012360 testing method Methods 0.000 description 16
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 12
- YLJJAVFOBDSYAN-UHFFFAOYSA-N dichloro-ethenyl-methylsilane Chemical compound C[Si](Cl)(Cl)C=C YLJJAVFOBDSYAN-UHFFFAOYSA-N 0.000 description 9
- 239000012212 insulator Substances 0.000 description 8
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000155 melt Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 3
- XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000004020 conductor Substances 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000004711 α-olefin Substances 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- LIKFHECYJZWXFJ-UHFFFAOYSA-N dimethyldichlorosilane Chemical compound C[Si](C)(Cl)Cl LIKFHECYJZWXFJ-UHFFFAOYSA-N 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000005325 percolation Methods 0.000 description 2
- 150000002978 peroxides Chemical group 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 1
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical group CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 description 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- SDJUKATYFRSDAS-UHFFFAOYSA-N 2-tert-butyl-3-methylphenol Chemical compound CC1=CC=CC(O)=C1C(C)(C)C SDJUKATYFRSDAS-UHFFFAOYSA-N 0.000 description 1
- XOUQAVYLRNOXDO-UHFFFAOYSA-N 2-tert-butyl-5-methylphenol Chemical compound CC1=CC=C(C(C)(C)C)C(O)=C1 XOUQAVYLRNOXDO-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
- UJAWGGOCYUPCPS-UHFFFAOYSA-N 4-(2-phenylpropan-2-yl)-n-[4-(2-phenylpropan-2-yl)phenyl]aniline Chemical compound C=1C=C(NC=2C=CC(=CC=2)C(C)(C)C=2C=CC=CC=2)C=CC=1C(C)(C)C1=CC=CC=C1 UJAWGGOCYUPCPS-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000218645 Cedrus Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- 239000002656 Distearyl thiodipropionate Substances 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241000270666 Testudines Species 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 238000004090 dissolution Methods 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
- 238000004821 distillation Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000011067 equilibration Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229960000907 methylthioninium chloride Drugs 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 238000002360 preparation method Methods 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
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- NGSWKAQJJWESNS-ZZXKWVIFSA-N trans-4-coumaric acid Chemical compound OC(=O)\C=C\C1=CC=C(O)C=C1 NGSWKAQJJWESNS-ZZXKWVIFSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UIYCHXAGWOYNNA-UHFFFAOYSA-N vinyl sulfide Chemical group C=CSC=C UIYCHXAGWOYNNA-UHFFFAOYSA-N 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
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/06—Ethers; Acetals; Ketals; Ortho-esters
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
- C08K5/18—Amines; Quaternary ammonium compounds with aromatically bound amino groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
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)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Insulating Materials (AREA)
- Insulated Conductors (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US36295982A | 1982-03-31 | 1982-03-31 | |
| US362959 | 1982-03-31 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58201843A true JPS58201843A (ja) | 1983-11-24 |
| JPH0119691B2 JPH0119691B2 (enExample) | 1989-04-12 |
Family
ID=23428218
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58052821A Granted JPS58201843A (ja) | 1982-03-31 | 1983-03-30 | ウォータートリーイング抵抗性を有するエチレン系重合体組成物 |
| JP62316388A Pending JPS63178151A (ja) | 1982-03-31 | 1987-12-16 | エチレン系重合体組成物用ウオータートリー抑制添加剤組成物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62316388A Pending JPS63178151A (ja) | 1982-03-31 | 1987-12-16 | エチレン系重合体組成物用ウオータートリー抑制添加剤組成物 |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP0090427B1 (enExample) |
| JP (2) | JPS58201843A (enExample) |
| AU (1) | AU550853B2 (enExample) |
| BR (1) | BR8301639A (enExample) |
| CA (1) | CA1181940A (enExample) |
| DE (1) | DE3365239D1 (enExample) |
| ES (1) | ES521159A0 (enExample) |
| GR (1) | GR77987B (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63178151A (ja) * | 1982-03-31 | 1988-07-22 | ユニオン・カーバイド・コーポレーシヨン | エチレン系重合体組成物用ウオータートリー抑制添加剤組成物 |
| JPS6433145A (en) * | 1987-05-18 | 1989-02-03 | Union Carbide Corp | Anti-tree composition |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0217585A3 (en) * | 1985-09-24 | 1989-08-30 | Du Pont Canada Inc. | Manufacture of film from linear low density polyethylene |
| US4797511A (en) * | 1987-09-25 | 1989-01-10 | Uniroyal Chemical Company, Inc. | Polyethylene stabilized by mixture of hindered phenol and amine antioxidants |
| JPH0794582B2 (ja) * | 1990-08-24 | 1995-10-11 | ダイキン工業株式会社 | 固着性の改良されたフルオロエラストマー組成物 |
| JP2634771B2 (ja) * | 1993-06-16 | 1997-07-30 | 日本冶金工業株式会社 | 電磁調理器用容器及びその製造方法 |
| TW403916B (en) * | 1995-03-30 | 2000-09-01 | Union Carbide Chem Plastic | Tree resistant cable |
| GB0022687D0 (en) * | 2000-09-15 | 2000-11-01 | Biccgeneral Uk Cables Ltd | Polymer composition and a method and apparatus for testing the resistance of the of the polymer composition to electrical stress induced degradation |
| EP1769512A1 (en) | 2004-06-09 | 2007-04-04 | Dow Corning Corporation | Anti-corrosion additive for electrical cable restoration fluids |
| EP2935424B1 (en) | 2012-12-21 | 2020-08-26 | Dow Global Technologies LLC | Polyolefin-based cable compound formulation for improved foamability and enhanced processability |
| CN109593265B (zh) * | 2018-12-14 | 2021-07-27 | 成都鑫成鹏高分子科技股份有限公司 | 一种低收缩硅烷交联电缆料及其制备方法 |
| EP4201214A4 (en) | 2020-08-24 | 2024-03-13 | Tiecher, Mauro | System for adjusting bearings for poultry offal processing machines |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5628231A (en) * | 1979-08-16 | 1981-03-19 | Nippon Yunikaa Kk | Polyolefin composition for electrical insulation |
| 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 |
-
1983
- 1983-03-25 CA CA000424555A patent/CA1181940A/en not_active Expired
- 1983-03-30 DE DE8383103194T patent/DE3365239D1/de not_active Expired
- 1983-03-30 EP EP83103194A patent/EP0090427B1/en not_active Expired
- 1983-03-30 ES ES521159A patent/ES521159A0/es active Granted
- 1983-03-30 GR GR70943A patent/GR77987B/el unknown
- 1983-03-30 AU AU13030/83A patent/AU550853B2/en not_active Expired
- 1983-03-30 BR BR8301639A patent/BR8301639A/pt unknown
- 1983-03-30 JP JP58052821A patent/JPS58201843A/ja active Granted
-
1987
- 1987-12-16 JP JP62316388A patent/JPS63178151A/ja active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63178151A (ja) * | 1982-03-31 | 1988-07-22 | ユニオン・カーバイド・コーポレーシヨン | エチレン系重合体組成物用ウオータートリー抑制添加剤組成物 |
| JPS6433145A (en) * | 1987-05-18 | 1989-02-03 | Union Carbide Corp | Anti-tree composition |
Also Published As
| Publication number | Publication date |
|---|---|
| CA1181940A (en) | 1985-02-05 |
| DE3365239D1 (en) | 1986-09-18 |
| AU1303083A (en) | 1983-10-06 |
| EP0090427A1 (en) | 1983-10-05 |
| ES8405828A1 (es) | 1984-06-16 |
| JPH0119691B2 (enExample) | 1989-04-12 |
| EP0090427B1 (en) | 1986-08-13 |
| JPS63178151A (ja) | 1988-07-22 |
| ES521159A0 (es) | 1984-06-16 |
| GR77987B (enExample) | 1984-09-25 |
| BR8301639A (pt) | 1983-12-13 |
| AU550853B2 (en) | 1986-04-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4440671A (en) | Compositions of hydrocarbon-substituted diphenyl amines and high molecular weight polyethylene glycols; and the use thereof as water-tree retardants for polymers | |
| CN105246960B (zh) | 2,5-呋喃二甲酸二烷基酯增塑剂和增塑的聚合组合物 | |
| JPS59501955A (ja) | ポリフェニレンエ−テル樹脂組成物 | |
| JPH0119691B2 (enExample) | ||
| JP2002514262A (ja) | エチレン−酢酸ビニルコポリマーとエチレン−酢酸ビニル−一酸化炭素ターポリマーとの配合物 | |
| KR0122076B1 (ko) | 힌더 페놀 및 아민 산화방지제 혼합물을 포함하는 폴리에틸렌의 안정화 조성물 | |
| EP0278555A1 (en) | Polyamide compositions | |
| CN114829462A (zh) | 聚烯烃组合物 | |
| US3118866A (en) | Polyethylene composition and process of crosslinking | |
| JPS59157151A (ja) | 電気伝導性有機熱可塑性組成物 | |
| EP0124106A1 (en) | Poly(arylene sulfide) compositions | |
| JPS6158496B2 (enExample) | ||
| JPS5869236A (ja) | ウオ−タ−トリ−イングがｎ−フエニル置換アミノシランにより安定化されたエチレン重合体及び電気導体の絶縁体としてのこれら組成物の使用 | |
| JPS62500894A (ja) | 電気ワイヤ−およびケ−ブル | |
| CN110073446A (zh) | 可固化的半导体组合物 | |
| WO1992009653A1 (en) | Improvement in or relating to polyester compositions | |
| EP0278559A2 (en) | Polyamide compositions | |
| EP0090382B1 (en) | Organo siloxanes, method for the preparation thereof and polymeric compositions containing same | |
| BR112019007054B1 (pt) | Composição de masterbatch de aditivo, composição de poliolefina curável por umidade, método de preparação de uma composição poliolefínica curável por umidade, artigo fabricado, condutor revestido e método de conduzir eletricidade | |
| JP2022502527A (ja) | 誘電性強化ポリエチレン配合物 | |
| US4492647A (en) | Organopolysiloxanes useful as dielectric fluids and anti-treeing additives | |
| US3915945A (en) | Dielectric polyolefin compositions | |
| US4483954A (en) | Silanes useful as water tree and electrical tree resistant additives | |
| TWI805586B (zh) | 可交聯組合物、製品以及導電方法 | |
| JPS59206445A (ja) | トリ−化防止剤 |