NO333375B1 - Stabilisert isolasjonssammensetning for en mellom- og hoyspenningskabel - Google Patents
Stabilisert isolasjonssammensetning for en mellom- og hoyspenningskabel Download PDFInfo
- Publication number
- NO333375B1 NO333375B1 NO20021657A NO20021657A NO333375B1 NO 333375 B1 NO333375 B1 NO 333375B1 NO 20021657 A NO20021657 A NO 20021657A NO 20021657 A NO20021657 A NO 20021657A NO 333375 B1 NO333375 B1 NO 333375B1
- Authority
- NO
- Norway
- Prior art keywords
- tert
- alkyl
- bis
- phenyl
- polyethylene
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 56
- 238000009413 insulation Methods 0.000 title claims abstract description 9
- -1 polyethylene Polymers 0.000 claims abstract description 107
- 239000004698 Polyethylene Substances 0.000 claims abstract description 30
- 229920000573 polyethylene Polymers 0.000 claims abstract description 30
- 239000003063 flame retardant Substances 0.000 claims abstract description 27
- 150000001451 organic peroxides Chemical class 0.000 claims abstract description 13
- 238000002844 melting Methods 0.000 claims abstract description 9
- 230000008018 melting Effects 0.000 claims abstract description 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 29
- 125000000217 alkyl group Chemical group 0.000 claims description 28
- 238000004132 cross linking Methods 0.000 claims description 28
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims description 23
- 150000001875 compounds Chemical class 0.000 claims description 21
- 150000002978 peroxides Chemical class 0.000 claims description 19
- GQBHYWDCHSZDQU-UHFFFAOYSA-N 4-(2,4,4-trimethylpentan-2-yl)-n-[4-(2,4,4-trimethylpentan-2-yl)phenyl]aniline Chemical compound C1=CC(C(C)(C)CC(C)(C)C)=CC=C1NC1=CC=C(C(C)(C)CC(C)(C)C)C=C1 GQBHYWDCHSZDQU-UHFFFAOYSA-N 0.000 claims description 16
- 125000006705 (C5-C7) cycloalkyl group Chemical group 0.000 claims description 15
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 15
- 239000001257 hydrogen Substances 0.000 claims description 15
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 14
- 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 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- GAODDBNJCKQQDY-UHFFFAOYSA-N 2-methyl-4,6-bis(octylsulfanylmethyl)phenol Chemical compound CCCCCCCCSCC1=CC(C)=C(O)C(CSCCCCCCCC)=C1 GAODDBNJCKQQDY-UHFFFAOYSA-N 0.000 claims description 11
- 125000003944 tolyl group Chemical group 0.000 claims description 11
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims description 10
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims description 10
- 230000002028 premature Effects 0.000 claims description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
- 150000001412 amines Chemical class 0.000 claims description 8
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 8
- 238000000354 decomposition reaction Methods 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 5
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- OPEKHRGERHDLRK-UHFFFAOYSA-N 4-tert-butyl-n-(4-tert-butylphenyl)aniline Chemical compound C1=CC(C(C)(C)C)=CC=C1NC1=CC=C(C(C)(C)C)C=C1 OPEKHRGERHDLRK-UHFFFAOYSA-N 0.000 claims description 4
- UOMXLEWVJZEVGP-UHFFFAOYSA-N 4-tert-butyl-n-phenylaniline Chemical compound C1=CC(C(C)(C)C)=CC=C1NC1=CC=CC=C1 UOMXLEWVJZEVGP-UHFFFAOYSA-N 0.000 claims description 4
- OSFOTMWFXQGWKZ-UHFFFAOYSA-N n-phenyl-4-(2,4,4-trimethylpentan-2-yl)aniline Chemical compound C1=CC(C(C)(C)CC(C)(C)C)=CC=C1NC1=CC=CC=C1 OSFOTMWFXQGWKZ-UHFFFAOYSA-N 0.000 claims description 4
- VTFXHGBOGGGYDO-UHFFFAOYSA-N 2,4-bis(dodecylsulfanylmethyl)-6-methylphenol Chemical compound CCCCCCCCCCCCSCC1=CC(C)=C(O)C(CSCCCCCCCCCCCC)=C1 VTFXHGBOGGGYDO-UHFFFAOYSA-N 0.000 claims description 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 2
- 229920003020 cross-linked polyethylene Polymers 0.000 claims 2
- 239000004703 cross-linked polyethylene Substances 0.000 claims 2
- AKFWYZBRXBSZJX-UHFFFAOYSA-N 2-[[3-tert-butyl-5-(carboxymethylsulfanylmethyl)-4-hydroxyphenyl]methylsulfanyl]acetic acid Chemical compound CC(C)(C)C1=CC(CSCC(O)=O)=CC(CSCC(O)=O)=C1O AKFWYZBRXBSZJX-UHFFFAOYSA-N 0.000 description 17
- 229920000642 polymer Polymers 0.000 description 11
- 150000002148 esters Chemical class 0.000 description 8
- 229920001684 low density polyethylene Polymers 0.000 description 8
- 238000001125 extrusion Methods 0.000 description 7
- 239000004702 low-density polyethylene Substances 0.000 description 7
- 239000003381 stabilizer Substances 0.000 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 description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
- YFHKLSPMRRWLKI-UHFFFAOYSA-N 2-tert-butyl-4-(3-tert-butyl-4-hydroxy-5-methylphenyl)sulfanyl-6-methylphenol Chemical class 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 5
- 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 5
- 238000004073 vulcanization Methods 0.000 description 5
- ZBHJTSZJYILOET-UHFFFAOYSA-N 3-[[3-tert-butyl-5-(2-carboxyethylsulfanylmethyl)-4-hydroxyphenyl]methylsulfanyl]propanoic acid Chemical compound CC(C)(C)C1=CC(CSCCC(O)=O)=CC(CSCCC(O)=O)=C1O ZBHJTSZJYILOET-UHFFFAOYSA-N 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- 239000004020 conductor Substances 0.000 description 4
- 239000003431 cross linking reagent Substances 0.000 description 4
- 229920001519 homopolymer Polymers 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 238000001723 curing Methods 0.000 description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
- QKIUAMUSENSFQQ-UHFFFAOYSA-N dimethylazanide Chemical compound C[N-]C QKIUAMUSENSFQQ-UHFFFAOYSA-N 0.000 description 3
- 230000029142 excretion Effects 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- NNBYRCDMGTYHRV-UHFFFAOYSA-N n'-[2-(3-aminopropylamino)ethyl]propane-1,3-diamine;2-n,4-n-dibutyl-6-methyl-2-n,4-n-bis(1,2,2,6,6-pentamethylpiperidin-4-yl)-1,3,5-triazine-2,4-diamine Chemical compound NCCCNCCNCCCN.N=1C(C)=NC(N(CCCC)C2CC(C)(C)N(C)C(C)(C)C2)=NC=1N(CCCC)C1CC(C)(C)N(C)C(C)(C)C1 NNBYRCDMGTYHRV-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 230000035900 sweating Effects 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- CVKLQWPMXWTXJK-UHFFFAOYSA-N 2-[[3-tert-butyl-5-(1-carboxyethylsulfanylmethyl)-4-hydroxyphenyl]methylsulfanyl]propanoic acid Chemical compound OC(=O)C(C)SCC1=CC(CSC(C)C(O)=O)=C(O)C(C(C)(C)C)=C1 CVKLQWPMXWTXJK-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 2
- SPJPATBUSZJVAW-UHFFFAOYSA-N 3-[[3-tert-butyl-5-(3-carboxybutan-2-ylsulfanylmethyl)-4-hydroxyphenyl]methylsulfanyl]-2-methylbutanoic acid Chemical compound OC(=O)C(C)C(C)SCC1=CC(CSC(C)C(C)C(O)=O)=C(O)C(C(C)(C)C)=C1 SPJPATBUSZJVAW-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- 125000000304 alkynyl group Chemical group 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000003749 cleanliness Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 125000001841 imino group Chemical group [H]N=* 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- KDGNCLDCOVTOCS-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy propan-2-yl carbonate Chemical compound CC(C)OC(=O)OOC(C)(C)C KDGNCLDCOVTOCS-UHFFFAOYSA-N 0.000 description 1
- OXYKVVLTXXXVRT-UHFFFAOYSA-N (4-chlorobenzoyl) 4-chlorobenzenecarboperoxoate Chemical compound C1=CC(Cl)=CC=C1C(=O)OOC(=O)C1=CC=C(Cl)C=C1 OXYKVVLTXXXVRT-UHFFFAOYSA-N 0.000 description 1
- RIPYNJLMMFGZSX-UHFFFAOYSA-N (5-benzoylperoxy-2,5-dimethylhexan-2-yl) benzenecarboperoxoate Chemical compound C=1C=CC=CC=1C(=O)OOC(C)(C)CCC(C)(C)OOC(=O)C1=CC=CC=C1 RIPYNJLMMFGZSX-UHFFFAOYSA-N 0.000 description 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
- BLKRGXCGFRXRNQ-SNAWJCMRSA-N (z)-3-carbonoperoxoyl-4,4-dimethylpent-2-enoic acid Chemical compound OC(=O)/C=C(C(C)(C)C)\C(=O)OO BLKRGXCGFRXRNQ-SNAWJCMRSA-N 0.000 description 1
- WKKRYWQLVOISAU-UHFFFAOYSA-N 1,3,5-tris(2-tert-butylperoxypropan-2-yl)benzene Chemical compound CC(C)(C)OOC(C)(C)C1=CC(C(C)(C)OOC(C)(C)C)=CC(C(C)(C)OOC(C)(C)C)=C1 WKKRYWQLVOISAU-UHFFFAOYSA-N 0.000 description 1
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N 1,4-Benzenediol Natural products OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 1
- UICXTANXZJJIBC-UHFFFAOYSA-N 1-(1-hydroperoxycyclohexyl)peroxycyclohexan-1-ol Chemical compound C1CCCCC1(O)OOC1(OO)CCCCC1 UICXTANXZJJIBC-UHFFFAOYSA-N 0.000 description 1
- RZLFNZFPQFDUFW-UHFFFAOYSA-N 2,4-bis(1,3-benzothiazol-2-ylsulfanylmethyl)-6-tert-butylphenol Chemical compound C1=CC=C2SC(SCC=3C=C(CSC=4SC5=CC=CC=C5N=4)C=C(C=3O)C(C)(C)C)=NC2=C1 RZLFNZFPQFDUFW-UHFFFAOYSA-N 0.000 description 1
- CPALSSDUQKWXFM-UHFFFAOYSA-N 2,4-bis(benzylsulfanylmethyl)-6-methylphenol Chemical compound C=1C(CSCC=2C=CC=CC=2)=C(O)C(C)=CC=1CSCC1=CC=CC=C1 CPALSSDUQKWXFM-UHFFFAOYSA-N 0.000 description 1
- CWTXAAIRSCFWLN-UHFFFAOYSA-N 2,4-bis(benzylsulfanylmethyl)-6-tert-butylphenol Chemical compound C=1C(CSCC=2C=CC=CC=2)=C(O)C(C(C)(C)C)=CC=1CSCC1=CC=CC=C1 CWTXAAIRSCFWLN-UHFFFAOYSA-N 0.000 description 1
- CTEWOKQOBCDFBF-UHFFFAOYSA-N 2,4-bis(butan-2-ylsulfanylmethyl)-6-tert-butylphenol Chemical compound CCC(C)SCC1=CC(CSC(C)CC)=C(O)C(C(C)(C)C)=C1 CTEWOKQOBCDFBF-UHFFFAOYSA-N 0.000 description 1
- VJPJFFZUPSNVBX-UHFFFAOYSA-N 2,4-bis(dodecylsulfanylmethyl)-6-(2-ethylhexyl)phenol Chemical compound CCCCCCCCCCCCSCC1=CC(CSCCCCCCCCCCCC)=C(O)C(CC(CC)CCCC)=C1 VJPJFFZUPSNVBX-UHFFFAOYSA-N 0.000 description 1
- SHOFCMBBNVNGRM-UHFFFAOYSA-N 2,4-bis(dodecylsulfanylmethyl)-6-(2-methylbutan-2-yl)phenol Chemical compound CCCCCCCCCCCCSCC1=CC(CSCCCCCCCCCCCC)=C(O)C(C(C)(C)CC)=C1 SHOFCMBBNVNGRM-UHFFFAOYSA-N 0.000 description 1
- VEYURQYVHJAECH-UHFFFAOYSA-N 2,4-bis(dodecylsulfanylmethyl)-6-(2-methylpentan-2-yl)phenol Chemical compound CCCCCCCCCCCCSCC1=CC(CSCCCCCCCCCCCC)=C(O)C(C(C)(C)CCC)=C1 VEYURQYVHJAECH-UHFFFAOYSA-N 0.000 description 1
- ILIVLFQJLLUVKN-UHFFFAOYSA-N 2,4-bis(dodecylsulfanylmethyl)-6-(4-methylphenyl)phenol Chemical compound CCCCCCCCCCCCSCC1=CC(CSCCCCCCCCCCCC)=C(O)C(C=2C=CC(C)=CC=2)=C1 ILIVLFQJLLUVKN-UHFFFAOYSA-N 0.000 description 1
- KGAUIOQJPCLOAQ-UHFFFAOYSA-N 2,4-bis(dodecylsulfanylmethyl)-6-phenylphenol Chemical compound CCCCCCCCCCCCSCC1=CC(CSCCCCCCCCCCCC)=C(O)C(C=2C=CC=CC=2)=C1 KGAUIOQJPCLOAQ-UHFFFAOYSA-N 0.000 description 1
- DEHMQOBXMQCZOO-UHFFFAOYSA-N 2,4-bis(dodecylsulfanylmethyl)-6-prop-2-enylphenol Chemical compound CCCCCCCCCCCCSCC1=CC(CSCCCCCCCCCCCC)=C(O)C(CC=C)=C1 DEHMQOBXMQCZOO-UHFFFAOYSA-N 0.000 description 1
- WJKUELLRFKSAID-UHFFFAOYSA-N 2,4-bis(dodecylsulfanylmethyl)-6-propan-2-ylphenol Chemical compound CCCCCCCCCCCCSCC1=CC(CSCCCCCCCCCCCC)=C(O)C(C(C)C)=C1 WJKUELLRFKSAID-UHFFFAOYSA-N 0.000 description 1
- XLGUCKPCTUPVPQ-UHFFFAOYSA-N 2,4-bis(octylsulfanylmethyl)-6-phenylphenol Chemical compound CCCCCCCCSCC1=CC(CSCCCCCCCC)=C(O)C(C=2C=CC=CC=2)=C1 XLGUCKPCTUPVPQ-UHFFFAOYSA-N 0.000 description 1
- MYKNPTDEYBNKKU-UHFFFAOYSA-N 2,4-bis(octylsulfanylmethyl)-6-prop-2-enylphenol Chemical compound CCCCCCCCSCC1=CC(CSCCCCCCCC)=C(O)C(CC=C)=C1 MYKNPTDEYBNKKU-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
- TUAPLLGBMYGPST-UHFFFAOYSA-N 2,5-dimethyl-2,5-bis(2-methylbutan-2-ylperoxy)hexane Chemical compound CCC(C)(C)OOC(C)(C)CCC(C)(C)OOC(C)(C)CC TUAPLLGBMYGPST-UHFFFAOYSA-N 0.000 description 1
- SLQFXVVIVBSBFH-UHFFFAOYSA-N 2,6-ditert-butyl-4-[2-[[3-tert-butyl-5-[2-(3,5-ditert-butyl-4-hydroxyphenyl)ethylsulfanylmethyl]-4-hydroxyphenyl]methylsulfanyl]ethyl]phenol Chemical compound C=1C(CSCCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C(O)C(C(C)(C)C)=CC=1CSCCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SLQFXVVIVBSBFH-UHFFFAOYSA-N 0.000 description 1
- PQTBJHKPISMUGU-UHFFFAOYSA-N 2-(2-ethylhexyl)-4,6-bis(octylsulfanylmethyl)phenol Chemical compound CCCCCCCCSCC1=CC(CSCCCCCCCC)=C(O)C(CC(CC)CCCC)=C1 PQTBJHKPISMUGU-UHFFFAOYSA-N 0.000 description 1
- VORDWPFVOXISLM-UHFFFAOYSA-N 2-(2-methylpentan-2-yl)-4,6-bis(octylsulfanylmethyl)phenol Chemical compound CCCCCCCCSCC1=CC(CSCCCCCCCC)=C(O)C(C(C)(C)CCC)=C1 VORDWPFVOXISLM-UHFFFAOYSA-N 0.000 description 1
- SHCPGNGCMHININ-UHFFFAOYSA-N 2-(4-methylphenyl)-4,6-bis(octylsulfanylmethyl)phenol Chemical compound CCCCCCCCSCC1=CC(CSCCCCCCCC)=C(O)C(C=2C=CC(C)=CC=2)=C1 SHCPGNGCMHININ-UHFFFAOYSA-N 0.000 description 1
- ZEKHKSIENLGKRM-UHFFFAOYSA-N 2-[[3-(2-acetyloxyethylsulfanylmethyl)-5-tert-butyl-4-hydroxyphenyl]methylsulfanyl]ethyl acetate Chemical compound CC(=O)OCCSCC1=CC(CSCCOC(C)=O)=C(O)C(C(C)(C)C)=C1 ZEKHKSIENLGKRM-UHFFFAOYSA-N 0.000 description 1
- NGWNICNKXKEEMM-UHFFFAOYSA-N 2-[[3-tert-butyl-4-hydroxy-5-(1-oxopropan-2-ylsulfanylmethyl)phenyl]methylsulfanyl]propanal Chemical compound O=CC(C)SCC1=CC(CSC(C)C=O)=C(O)C(C(C)(C)C)=C1 NGWNICNKXKEEMM-UHFFFAOYSA-N 0.000 description 1
- IKSPANFZXPSGLH-UHFFFAOYSA-N 2-benzyl-4,6-bis(dodecylsulfanylmethyl)phenol Chemical compound CCCCCCCCCCCCSCC1=CC(CSCCCCCCCCCCCC)=C(O)C(CC=2C=CC=CC=2)=C1 IKSPANFZXPSGLH-UHFFFAOYSA-N 0.000 description 1
- DYFZTQLLBHZCAY-UHFFFAOYSA-N 2-benzyl-4,6-bis(octylsulfanylmethyl)phenol Chemical compound CCCCCCCCSCC1=CC(CSCCCCCCCC)=C(O)C(CC=2C=CC=CC=2)=C1 DYFZTQLLBHZCAY-UHFFFAOYSA-N 0.000 description 1
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 1
- QOOIECWFYOYLNV-UHFFFAOYSA-N 2-cyclohexyl-4,6-bis(dodecylsulfanylmethyl)phenol Chemical compound CCCCCCCCCCCCSCC1=CC(CSCCCCCCCCCCCC)=C(O)C(C2CCCCC2)=C1 QOOIECWFYOYLNV-UHFFFAOYSA-N 0.000 description 1
- VOMGSCULUZCURL-UHFFFAOYSA-N 2-cyclohexyl-4,6-bis(octylsulfanylmethyl)phenol Chemical compound CCCCCCCCSCC1=CC(CSCCCCCCCC)=C(O)C(C2CCCCC2)=C1 VOMGSCULUZCURL-UHFFFAOYSA-N 0.000 description 1
- KRDXTHSSNCTAGY-UHFFFAOYSA-N 2-cyclohexylpyrrolidine Chemical compound C1CCNC1C1CCCCC1 KRDXTHSSNCTAGY-UHFFFAOYSA-N 0.000 description 1
- SQVVNFZBSPUHDK-UHFFFAOYSA-N 2-ethylhexyl 2-[[3-[[2-(2-ethylhexoxy)-2-oxoethyl]sulfanylmethyl]-4-hydroxy-5-methylphenyl]methylsulfanyl]acetate Chemical compound CCCCC(CC)COC(=O)CSCC1=CC(C)=C(O)C(CSCC(=O)OCC(CC)CCCC)=C1 SQVVNFZBSPUHDK-UHFFFAOYSA-N 0.000 description 1
- JJRDRFZYKKFYMO-UHFFFAOYSA-N 2-methyl-2-(2-methylbutan-2-ylperoxy)butane Chemical compound CCC(C)(C)OOC(C)(C)CC JJRDRFZYKKFYMO-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- OBCGHTWADUANHH-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(2-ethylhexylsulfanylmethyl)phenol Chemical compound CCCCC(CC)CSCC1=CC(CSCC(CC)CCCC)=C(O)C(C(C)(C)C)=C1 OBCGHTWADUANHH-UHFFFAOYSA-N 0.000 description 1
- VUNXZIAWEWTTRR-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(2-hydroxyethylsulfanylmethyl)phenol Chemical compound CC(C)(C)C1=CC(CSCCO)=CC(CSCCO)=C1O VUNXZIAWEWTTRR-UHFFFAOYSA-N 0.000 description 1
- OEMRNJYOAJHCMP-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(butylsulfanylmethyl)phenol Chemical compound CCCCSCC1=CC(CSCCCC)=C(O)C(C(C)(C)C)=C1 OEMRNJYOAJHCMP-UHFFFAOYSA-N 0.000 description 1
- UJVLWJVGJQJTKV-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(cyclohexylsulfanylmethyl)phenol Chemical compound C=1C(CSC2CCCCC2)=C(O)C(C(C)(C)C)=CC=1CSC1CCCCC1 UJVLWJVGJQJTKV-UHFFFAOYSA-N 0.000 description 1
- VTQRESWFHDTZOP-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(decylsulfanylmethyl)phenol Chemical compound CCCCCCCCCCSCC1=CC(CSCCCCCCCCCC)=C(O)C(C(C)(C)C)=C1 VTQRESWFHDTZOP-UHFFFAOYSA-N 0.000 description 1
- VIPWOQWDGJKMNW-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(dodecylsulfanylmethyl)phenol Chemical compound CCCCCCCCCCCCSCC1=CC(CSCCCCCCCCCCCC)=C(O)C(C(C)(C)C)=C1 VIPWOQWDGJKMNW-UHFFFAOYSA-N 0.000 description 1
- NRUHXQWZAZOAPO-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(ethylsulfanylmethyl)phenol Chemical compound CCSCC1=CC(CSCC)=C(O)C(C(C)(C)C)=C1 NRUHXQWZAZOAPO-UHFFFAOYSA-N 0.000 description 1
- ONVPBHGYOGCYHG-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(hexadecylsulfanylmethyl)phenol Chemical compound CCCCCCCCCCCCCCCCSCC1=CC(CSCCCCCCCCCCCCCCCC)=C(O)C(C(C)(C)C)=C1 ONVPBHGYOGCYHG-UHFFFAOYSA-N 0.000 description 1
- KHASFNSBLQNSHW-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(hexylsulfanylmethyl)phenol Chemical compound CCCCCCSCC1=CC(CSCCCCCC)=C(O)C(C(C)(C)C)=C1 KHASFNSBLQNSHW-UHFFFAOYSA-N 0.000 description 1
- IBDZMVMIJIDGGR-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(icosylsulfanylmethyl)phenol Chemical compound CCCCCCCCCCCCCCCCCCCCSCC1=CC(CSCCCCCCCCCCCCCCCCCCCC)=C(O)C(C(C)(C)C)=C1 IBDZMVMIJIDGGR-UHFFFAOYSA-N 0.000 description 1
- ZIHBXNBKVBTZNR-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(methylsulfanylmethyl)phenol Chemical compound CSCC1=CC(CSC)=C(O)C(C(C)(C)C)=C1 ZIHBXNBKVBTZNR-UHFFFAOYSA-N 0.000 description 1
- ZEFCPDNXDIXUSZ-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(octadecylsulfanylmethyl)phenol Chemical compound CCCCCCCCCCCCCCCCCCSCC1=CC(CSCCCCCCCCCCCCCCCCCC)=C(O)C(C(C)(C)C)=C1 ZEFCPDNXDIXUSZ-UHFFFAOYSA-N 0.000 description 1
- ZYJXQDCMXTWHIV-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(octylsulfanylmethyl)phenol Chemical compound CCCCCCCCSCC1=CC(CSCCCCCCCC)=C(O)C(C(C)(C)C)=C1 ZYJXQDCMXTWHIV-UHFFFAOYSA-N 0.000 description 1
- FDNIHGGWNUXZMN-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(phenylsulfanylmethyl)phenol Chemical compound C=1C(CSC=2C=CC=CC=2)=C(O)C(C(C)(C)C)=CC=1CSC1=CC=CC=C1 FDNIHGGWNUXZMN-UHFFFAOYSA-N 0.000 description 1
- HGYCIUGAHIOJSW-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(prop-2-enylsulfanylmethyl)phenol Chemical compound CC(C)(C)C1=CC(CSCC=C)=CC(CSCC=C)=C1O HGYCIUGAHIOJSW-UHFFFAOYSA-N 0.000 description 1
- OLSHZEQMMKHCDJ-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(propan-2-ylsulfanylmethyl)phenol Chemical compound CC(C)SCC1=CC(CSC(C)C)=C(O)C(C(C)(C)C)=C1 OLSHZEQMMKHCDJ-UHFFFAOYSA-N 0.000 description 1
- PHVKQQZJMOESQM-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(tert-butylsulfanylmethyl)phenol Chemical compound CC(C)(C)SCC1=CC(CSC(C)(C)C)=C(O)C(C(C)(C)C)=C1 PHVKQQZJMOESQM-UHFFFAOYSA-N 0.000 description 1
- ISYPQCHHXCSGTF-UHFFFAOYSA-N 2-tert-butyl-4,6-bis(tetradecylsulfanylmethyl)phenol Chemical compound CCCCCCCCCCCCCCSCC1=CC(CSCCCCCCCCCCCCCC)=C(O)C(C(C)(C)C)=C1 ISYPQCHHXCSGTF-UHFFFAOYSA-N 0.000 description 1
- OKKTWRDEUFRMIA-UHFFFAOYSA-N 2-tert-butyl-4,6-bis[(2-hydroxycyclohexyl)sulfanylmethyl]phenol Chemical compound C=1C(CSC2C(CCCC2)O)=C(O)C(C(C)(C)C)=CC=1CSC1CCCCC1O OKKTWRDEUFRMIA-UHFFFAOYSA-N 0.000 description 1
- HEORCJWNFHRQBC-UHFFFAOYSA-N 2-tert-butyl-4,6-bis[(3,5-ditert-butyl-4-hydroxyphenyl)sulfanylmethyl]phenol Chemical compound C=1C(CSC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C(O)C(C(C)(C)C)=CC=1CSC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 HEORCJWNFHRQBC-UHFFFAOYSA-N 0.000 description 1
- XWMIPLCUXPEVRH-UHFFFAOYSA-N 2-tert-butyl-4,6-bis[(4-chlorophenyl)sulfanylmethyl]phenol Chemical compound C=1C(CSC=2C=CC(Cl)=CC=2)=C(O)C(C(C)(C)C)=CC=1CSC1=CC=C(Cl)C=C1 XWMIPLCUXPEVRH-UHFFFAOYSA-N 0.000 description 1
- SYIAVRMBFSBTIF-UHFFFAOYSA-N 2-tert-butyl-4,6-bis[(4-methoxyphenyl)sulfanylmethyl]phenol Chemical compound C1=CC(OC)=CC=C1SCC1=CC(CSC=2C=CC(OC)=CC=2)=C(O)C(C(C)(C)C)=C1 SYIAVRMBFSBTIF-UHFFFAOYSA-N 0.000 description 1
- PHCJJMOSGYJCTH-UHFFFAOYSA-N 2-tert-butyl-4,6-bis[(4-methylphenyl)sulfanylmethyl]phenol Chemical compound C1=CC(C)=CC=C1SCC1=CC(CSC=2C=CC(C)=CC=2)=C(O)C(C(C)(C)C)=C1 PHCJJMOSGYJCTH-UHFFFAOYSA-N 0.000 description 1
- XYFRHHAYSXIKGH-UHFFFAOYSA-N 3-(5-methoxy-2-methoxycarbonyl-1h-indol-3-yl)prop-2-enoic acid Chemical compound C1=C(OC)C=C2C(C=CC(O)=O)=C(C(=O)OC)NC2=C1 XYFRHHAYSXIKGH-UHFFFAOYSA-N 0.000 description 1
- QWQQRBYTGIOUFI-UHFFFAOYSA-N 3-[[3-(2,3-dihydroxypropylsulfanylmethyl)-4-hydroxy-2,5-dimethylphenyl]methylsulfanyl]propane-1,2-diol Chemical compound CC1=CC(CSCC(O)CO)=C(C)C(CSCC(O)CO)=C1O QWQQRBYTGIOUFI-UHFFFAOYSA-N 0.000 description 1
- GHACUGQBJIXJGB-UHFFFAOYSA-N 3-[[3-tert-butyl-4-hydroxy-5-(3-oxobutan-2-ylsulfanylmethyl)phenyl]methylsulfanyl]butan-2-one Chemical compound CC(=O)C(C)SCC1=CC(CSC(C)C(C)=O)=C(O)C(C(C)(C)C)=C1 GHACUGQBJIXJGB-UHFFFAOYSA-N 0.000 description 1
- XDQMBMWWTZICAY-UHFFFAOYSA-N 3-[[3-tert-butyl-5-(2,3-dihydroxypropylsulfanylmethyl)-4-hydroxyphenyl]methylsulfanyl]propane-1,2-diol Chemical compound CC(C)(C)C1=CC(CSCC(O)CO)=CC(CSCC(O)CO)=C1O XDQMBMWWTZICAY-UHFFFAOYSA-N 0.000 description 1
- QDVRXJQKEIGTIM-UHFFFAOYSA-N 3-[[3-tert-butyl-5-(2-cyanoethylsulfanylmethyl)-4-hydroxyphenyl]methylsulfanyl]propanenitrile Chemical compound CC(C)(C)C1=CC(CSCCC#N)=CC(CSCCC#N)=C1O QDVRXJQKEIGTIM-UHFFFAOYSA-N 0.000 description 1
- CAMBAGZYTIDFBK-UHFFFAOYSA-N 3-tert-butylperoxy-2-methylpropan-1-ol Chemical compound CC(CO)COOC(C)(C)C CAMBAGZYTIDFBK-UHFFFAOYSA-N 0.000 description 1
- MKTOIPPVFPJEQO-UHFFFAOYSA-N 4-(3-carboxypropanoylperoxy)-4-oxobutanoic acid Chemical compound OC(=O)CCC(=O)OOC(=O)CCC(O)=O MKTOIPPVFPJEQO-UHFFFAOYSA-N 0.000 description 1
- CCOJJJCQUHWYAT-UHFFFAOYSA-N 4-methyl-4-(2-methylbutan-2-ylperoxy)pentan-2-ol Chemical compound CCC(C)(C)OOC(C)(C)CC(C)O CCOJJJCQUHWYAT-UHFFFAOYSA-N 0.000 description 1
- JNSWFNBIZLIBPH-UHFFFAOYSA-N 4-tert-butylperoxy-4-methylpentan-2-ol Chemical compound CC(O)CC(C)(C)OOC(C)(C)C JNSWFNBIZLIBPH-UHFFFAOYSA-N 0.000 description 1
- DWUSYXYBLHQJBV-UHFFFAOYSA-N 6-tert-butyl-3-methyl-2,4-bis(phenylsulfanylmethyl)phenol Chemical compound C1=C(C(C)(C)C)C(O)=C(CSC=2C=CC=CC=2)C(C)=C1CSC1=CC=CC=C1 DWUSYXYBLHQJBV-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- LMYHHCDPOACYBO-UHFFFAOYSA-N C(C#C)SCC1=C(C(=CC(=C1)CSCC#C)C(C)(C)C)O Chemical compound C(C#C)SCC1=C(C(=CC(=C1)CSCC#C)C(C)(C)C)O LMYHHCDPOACYBO-UHFFFAOYSA-N 0.000 description 1
- GURFSDXJFMXYJZ-UHFFFAOYSA-N C(CCCCCCCCCCC)SCC1=C(C(=CC(=C1)CSCCCCCCCCCCCC)CC#C)O Chemical compound C(CCCCCCCCCCC)SCC1=C(C(=CC(=C1)CSCCCCCCCCCCCC)CC#C)O GURFSDXJFMXYJZ-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-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
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000006547 cyclononyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 1
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- QZYRMODBFHTNHF-UHFFFAOYSA-N ditert-butyl benzene-1,2-dicarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1C(=O)OOC(C)(C)C QZYRMODBFHTNHF-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000000816 ethylene group Chemical class [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 125000006351 ethylthiomethyl group Chemical group [H]C([H])([H])C([H])([H])SC([H])([H])* 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 125000000687 hydroquinonyl group Chemical class C1(O)=C(C=C(O)C=C1)* 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- MJCJUDJQDGGKOX-UHFFFAOYSA-N n-dodecyldodecan-1-amine Chemical compound CCCCCCCCCCCCNCCCCCCCCCCCC MJCJUDJQDGGKOX-UHFFFAOYSA-N 0.000 description 1
- 125000003136 n-heptyl 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])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 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
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- XCZNNZGOSKIBGW-UHFFFAOYSA-N octadecyl 2-[[4-hydroxy-2,5-dimethyl-3-[(2-octadecoxy-2-oxoethyl)sulfanylmethyl]phenyl]methylsulfanyl]acetate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CSCC1=CC(C)=C(O)C(CSCC(=O)OCCCCCCCCCCCCCCCCCC)=C1C XCZNNZGOSKIBGW-UHFFFAOYSA-N 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
- 150000002989 phenols Chemical class 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 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
- 239000002516 radical scavenger Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000012086 standard solution Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- WYKYCHHWIJXDAO-UHFFFAOYSA-N tert-butyl 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)C WYKYCHHWIJXDAO-UHFFFAOYSA-N 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- JZFHXRUVMKEOFG-UHFFFAOYSA-N tert-butyl dodecaneperoxoate Chemical compound CCCCCCCCCCCC(=O)OOC(C)(C)C JZFHXRUVMKEOFG-UHFFFAOYSA-N 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000001029 thermal curing Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 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
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 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
-
- 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)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Insulating Materials (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP01810356 | 2001-04-10 | ||
EP01810511 | 2001-05-23 |
Publications (3)
Publication Number | Publication Date |
---|---|
NO20021657D0 NO20021657D0 (no) | 2002-04-08 |
NO20021657L NO20021657L (no) | 2002-10-11 |
NO333375B1 true NO333375B1 (no) | 2013-05-13 |
Family
ID=26077366
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20021657A NO333375B1 (no) | 2001-04-10 | 2002-04-08 | Stabilisert isolasjonssammensetning for en mellom- og hoyspenningskabel |
Country Status (15)
Country | Link |
---|---|
US (1) | US7056967B2 (zh) |
JP (1) | JP4051667B2 (zh) |
KR (1) | KR100923284B1 (zh) |
CN (1) | CN1250636C (zh) |
AR (1) | AR033211A1 (zh) |
AU (1) | AU784703B2 (zh) |
BR (1) | BR0201173B1 (zh) |
CA (1) | CA2380987C (zh) |
CZ (1) | CZ305019B6 (zh) |
MX (1) | MXPA02003611A (zh) |
MY (1) | MY133253A (zh) |
NO (1) | NO333375B1 (zh) |
SG (1) | SG103854A1 (zh) |
SK (1) | SK287686B6 (zh) |
TW (1) | TWI239019B (zh) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0508350D0 (en) * | 2005-04-26 | 2005-06-01 | Great Lakes Chemical Europ | Stabilized crosslinked polyolefin compositions |
KR100727207B1 (ko) * | 2006-02-24 | 2007-06-13 | 주식회사 엘지화학 | 스웨트-아웃 억제 및 전기 절연특성이 우수한 가교 폴리에틸렌 조성물 |
CA2596750C (en) * | 2006-02-24 | 2011-02-01 | Lg Chem, Ltd. | Cross-linked polyethylene having excellent inhibition of sweat-out and insulation properties |
WO2009012092A1 (en) * | 2007-07-13 | 2009-01-22 | Dow Global Technologies Inc. | Low dielectric loss power cable sheaths comprising high pressure polyolefins free of silane functionality |
KR101362560B1 (ko) | 2011-08-08 | 2014-02-14 | 주식회사 엘지화학 | 가교 폴리에틸렌 조성물 |
CN104334630B (zh) | 2012-06-04 | 2018-03-20 | 神华集团有限责任公司 | 一种加工性能改善的交联聚乙烯组合物 |
WO2013185302A1 (zh) | 2012-06-13 | 2013-12-19 | 北京低碳清洁能源研究所 | 一种交联聚乙烯组合物 |
CA2894934C (en) * | 2012-12-29 | 2020-07-07 | Dow Global Technologies Llc | Cross-linkable polymeric compositions, methods for making the same, and articles made therefrom |
GB201320919D0 (en) | 2013-11-27 | 2014-01-08 | Addivant Switzerland Gmbh | Composition |
JP6421217B2 (ja) * | 2017-06-07 | 2018-11-07 | ダウ グローバル テクノロジーズ エルエルシー | 架橋性高分子組成物、それを作製する方法、およびそれから作製される物品 |
KR101953630B1 (ko) | 2018-04-26 | 2019-03-04 | 정대기 | 다결정 실리콘 조성물 |
KR102060324B1 (ko) | 2018-04-26 | 2019-12-30 | 정대기 | 다결정 실리콘 절연체와 그의제조방법 및 그를 포함하는 애자,전력기기 및 부싱 |
KR102061478B1 (ko) | 2018-04-26 | 2020-01-02 | 정대기 | 다결정 실리콘 성형체 및 그의 제조방법 |
KR102055569B1 (ko) | 2018-04-26 | 2019-12-13 | (주) 이우티이씨 | 다결정 실리콘 절연체를 포함하는 애자 및 피뢰기 |
KR102133574B1 (ko) | 2018-05-29 | 2020-07-13 | 정대기 | 다결정 실리콘 절연체를 포함하는 케이블용 피복재 |
CN115219634A (zh) * | 2022-08-26 | 2022-10-21 | 南方电网科学研究院有限责任公司 | 电缆用可交联聚乙烯绝缘料抗烧焦性的评估方法 |
Family Cites Families (102)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR732895A (fr) * | 1932-10-18 | 1932-09-25 | Consortium Elektrochem Ind | Objets filés en alcool polyvinylique |
US4329383A (en) * | 1979-07-24 | 1982-05-11 | Nippon Zeon Co., Ltd. | Non-thrombogenic material comprising substrate which has been reacted with heparin |
EP0165209B1 (de) | 1984-06-12 | 1989-07-19 | Ciba-Geigy Ag | o,p-Bifunktionalisierte, o'-substituierte Phenole |
US4656242A (en) * | 1985-06-07 | 1987-04-07 | Henkel Corporation | Poly(ester-amide) compositions |
US4733665C2 (en) * | 1985-11-07 | 2002-01-29 | Expandable Grafts Partnership | Expandable intraluminal graft and method and apparatus for implanting an expandable intraluminal graft |
ES2014433B3 (es) * | 1985-11-13 | 1990-07-16 | Ciba-Geigy Ag | Fenoles sustituidos, como estabilizadores. |
DE3785320D1 (zh) * | 1986-12-24 | 1993-05-13 | Ciba-Geigy Ag, Basel, Ch | |
US5721131A (en) * | 1987-03-06 | 1998-02-24 | United States Of America As Represented By The Secretary Of The Navy | Surface modification of polymers with self-assembled monolayers that promote adhesion, outgrowth and differentiation of biological cells |
US4800882A (en) * | 1987-03-13 | 1989-01-31 | Cook Incorporated | Endovascular stent and delivery system |
US5019096A (en) * | 1988-02-11 | 1991-05-28 | Trustees Of Columbia University In The City Of New York | Infection-resistant compositions, medical devices and surfaces and methods for preparing and using same |
EP0346283B1 (de) * | 1988-06-09 | 1992-07-29 | Ciba-Geigy Ag | Schmierölzusammensetzung |
US4908404A (en) * | 1988-08-22 | 1990-03-13 | Biopolymers, Inc. | Synthetic amino acid-and/or peptide-containing graft copolymers |
IL90193A (en) * | 1989-05-04 | 1993-02-21 | Biomedical Polymers Int | Polurethane-based polymeric materials and biomedical articles and pharmaceutical compositions utilizing the same |
US5298260A (en) * | 1990-05-01 | 1994-03-29 | Mediventures, Inc. | Topical drug delivery with polyoxyalkylene polymer thermoreversible gels adjustable for pH and osmolality |
US5300295A (en) * | 1990-05-01 | 1994-04-05 | Mediventures, Inc. | Ophthalmic drug delivery with thermoreversible polyoxyalkylene gels adjustable for pH |
US5292516A (en) * | 1990-05-01 | 1994-03-08 | Mediventures, Inc. | Body cavity drug delivery with thermoreversible gels containing polyoxyalkylene copolymers |
US5306501A (en) * | 1990-05-01 | 1994-04-26 | Mediventures, Inc. | Drug delivery by injection with thermoreversible gels containing polyoxyalkylene copolymers |
US5258020A (en) * | 1990-09-14 | 1993-11-02 | Michael Froix | Method of using expandable polymeric stent with memory |
GB9027793D0 (en) * | 1990-12-21 | 1991-02-13 | Ucb Sa | Polyester-amides containing terminal carboxyl groups |
MX9702434A (es) * | 1991-03-07 | 1998-05-31 | Masimo Corp | Aparato de procesamiento de señales. |
US5417981A (en) * | 1992-04-28 | 1995-05-23 | Terumo Kabushiki Kaisha | Thermoplastic polymer composition and medical devices made of the same |
US5464650A (en) * | 1993-04-26 | 1995-11-07 | Medtronic, Inc. | Intravascular stent and method |
US5861168A (en) * | 1993-06-11 | 1999-01-19 | The Board Of Trustees Of The Leland Stanford Junior University | Intramural delivery of nitric oxide enhancer for inhibiting lesion formation after vascular injury |
US5380299A (en) * | 1993-08-30 | 1995-01-10 | Med Institute, Inc. | Thrombolytic treated intravascular medical device |
WO1995010989A1 (en) * | 1993-10-19 | 1995-04-27 | Scimed Life Systems, Inc. | Intravascular stent pump |
US6051576A (en) * | 1994-01-28 | 2000-04-18 | University Of Kentucky Research Foundation | Means to achieve sustained release of synergistic drugs by conjugation |
AU2068595A (en) | 1994-03-22 | 1995-10-09 | Ciba-Geigy Ag | Process for the stabilization of hdpe |
US5516881A (en) * | 1994-08-10 | 1996-05-14 | Cornell Research Foundation, Inc. | Aminoxyl-containing radical spin labeling in polymers and copolymers |
US5485496A (en) * | 1994-09-22 | 1996-01-16 | Cornell Research Foundation, Inc. | Gamma irradiation sterilizing of biomaterial medical devices or products, with improved degradation and mechanical properties |
US5482720A (en) * | 1994-10-11 | 1996-01-09 | Church & Dwight Co., Inc. | Encapsulated co-micronized bicarbonate salt compositions |
JPH10509696A (ja) * | 1994-10-12 | 1998-09-22 | フォーカル, インコーポレイテッド | 生分解性ポリマーを介する標的化送達 |
US5869127A (en) * | 1995-02-22 | 1999-02-09 | Boston Scientific Corporation | Method of providing a substrate with a bio-active/biocompatible coating |
US5837313A (en) * | 1995-04-19 | 1998-11-17 | Schneider (Usa) Inc | Drug release stent coating process |
US6010530A (en) * | 1995-06-07 | 2000-01-04 | Boston Scientific Technology, Inc. | Self-expanding endoluminal prosthesis |
US5609629A (en) * | 1995-06-07 | 1997-03-11 | Med Institute, Inc. | Coated implantable medical device |
US7611533B2 (en) * | 1995-06-07 | 2009-11-03 | Cook Incorporated | Coated implantable medical device |
US6774278B1 (en) * | 1995-06-07 | 2004-08-10 | Cook Incorporated | Coated implantable medical device |
US7550005B2 (en) * | 1995-06-07 | 2009-06-23 | Cook Incorporated | Coated implantable medical device |
US5877224A (en) * | 1995-07-28 | 1999-03-02 | Rutgers, The State University Of New Jersey | Polymeric drug formulations |
US5723219A (en) * | 1995-12-19 | 1998-03-03 | Talison Research | Plasma deposited film networks |
US6033582A (en) * | 1996-01-22 | 2000-03-07 | Etex Corporation | Surface modification of medical implants |
US6054553A (en) * | 1996-01-29 | 2000-04-25 | Bayer Ag | Process for the preparation of polymers having recurring agents |
US5610241A (en) * | 1996-05-07 | 1997-03-11 | Cornell Research Foundation, Inc. | Reactive graft polymer with biodegradable polymer backbone and method for preparing reactive biodegradable polymers |
US5876433A (en) * | 1996-05-29 | 1999-03-02 | Ethicon, Inc. | Stent and method of varying amounts of heparin coated thereon to control treatment |
US5874165A (en) * | 1996-06-03 | 1999-02-23 | Gore Enterprise Holdings, Inc. | Materials and method for the immobilization of bioactive species onto polymeric subtrates |
NL1003459C2 (nl) * | 1996-06-28 | 1998-01-07 | Univ Twente | Copoly(ester-amides) en copoly(ester-urethanen). |
US5711958A (en) * | 1996-07-11 | 1998-01-27 | Life Medical Sciences, Inc. | Methods for reducing or eliminating post-surgical adhesion formation |
US6530951B1 (en) * | 1996-10-24 | 2003-03-11 | Cook Incorporated | Silver implantable medical device |
US6240616B1 (en) * | 1997-04-15 | 2001-06-05 | Advanced Cardiovascular Systems, Inc. | Method of manufacturing a medicated porous metal prosthesis |
US6159978A (en) * | 1997-05-28 | 2000-12-12 | Aventis Pharmaceuticals Product, Inc. | Quinoline and quinoxaline compounds which inhibit platelet-derived growth factor and/or p56lck tyrosine kinases |
US6180632B1 (en) * | 1997-05-28 | 2001-01-30 | Aventis Pharmaceuticals Products Inc. | Quinoline and quinoxaline compounds which inhibit platelet-derived growth factor and/or p56lck tyrosine kinases |
US6211249B1 (en) * | 1997-07-11 | 2001-04-03 | Life Medical Sciences, Inc. | Polyester polyether block copolymers |
AU8901798A (en) * | 1997-08-08 | 1999-03-01 | Procter & Gamble Company, The | Laundry detergent compositions with amino acid based polymers to provide appearance and integrity benefits to fabrics laundered therewith |
US20030040790A1 (en) * | 1998-04-15 | 2003-02-27 | Furst Joseph G. | Stent coating |
WO1999055396A1 (en) * | 1998-04-27 | 1999-11-04 | Surmodics, Inc. | Bioactive agent release coating |
US6228917B1 (en) * | 1998-06-16 | 2001-05-08 | Union Carbide Chemicals & Plastics Technology Corporation | Polyethylene crosslinkable composition |
US6299604B1 (en) * | 1998-08-20 | 2001-10-09 | Cook Incorporated | Coated implantable medical device |
US6335029B1 (en) * | 1998-08-28 | 2002-01-01 | Scimed Life Systems, Inc. | Polymeric coatings for controlled delivery of active agents |
US6011125A (en) * | 1998-09-25 | 2000-01-04 | General Electric Company | Amide modified polyesters |
US6530950B1 (en) * | 1999-01-12 | 2003-03-11 | Quanam Medical Corporation | Intraluminal stent having coaxial polymer member |
US6143822A (en) * | 1999-03-18 | 2000-11-07 | Union Carbide Chemicals & Plastics Technology Corporation | Polyethylene crosslinkable composition |
EP1036805B1 (en) | 1999-03-18 | 2013-01-09 | Union Carbide Chemicals & Plastics Technology LLC | A polyethylene crosslinkable composition |
US6231978B1 (en) | 1999-03-31 | 2001-05-15 | Union Carbide Chemicals & Plastics Technology Corporation | Crosslinkable polyethylene composition |
JP2000306433A (ja) * | 1999-04-23 | 2000-11-02 | Sumitomo Electric Ind Ltd | 絶縁樹脂組成物とこれを用いた電線、ケーブルおよび電力ケーブルの接続部 |
US6283947B1 (en) * | 1999-07-13 | 2001-09-04 | Advanced Cardiovascular Systems, Inc. | Local drug delivery injection catheter |
US6494862B1 (en) * | 1999-07-13 | 2002-12-17 | Advanced Cardiovascular Systems, Inc. | Substance delivery apparatus and a method of delivering a therapeutic substance to an anatomical passageway |
US6177523B1 (en) * | 1999-07-14 | 2001-01-23 | Cardiotech International, Inc. | Functionalized polyurethanes |
US6191230B1 (en) * | 1999-07-22 | 2001-02-20 | Union Carbide Chemicals & Plastics Technology Corporation | Polyethylene crosslinkable composition |
US6713119B2 (en) * | 1999-09-03 | 2004-03-30 | Advanced Cardiovascular Systems, Inc. | Biocompatible coating for a prosthesis and a method of forming the same |
US6379381B1 (en) * | 1999-09-03 | 2002-04-30 | Advanced Cardiovascular Systems, Inc. | Porous prosthesis and a method of depositing substances into the pores |
US6503954B1 (en) * | 2000-03-31 | 2003-01-07 | Advanced Cardiovascular Systems, Inc. | Biocompatible carrier containing actinomycin D and a method of forming the same |
US6503556B2 (en) * | 2000-12-28 | 2003-01-07 | Advanced Cardiovascular Systems, Inc. | Methods of forming a coating for a prosthesis |
US6262157B1 (en) | 1999-09-29 | 2001-07-17 | Union Carbide Chemicals & Plastics Technology Corporation | Polyethylene crosslinkable composition |
US6203551B1 (en) * | 1999-10-04 | 2001-03-20 | Advanced Cardiovascular Systems, Inc. | Chamber for applying therapeutic substances to an implant device |
US6613432B2 (en) * | 1999-12-22 | 2003-09-02 | Biosurface Engineering Technologies, Inc. | Plasma-deposited coatings, devices and methods |
US6527801B1 (en) * | 2000-04-13 | 2003-03-04 | Advanced Cardiovascular Systems, Inc. | Biodegradable drug delivery material for stent |
US20020007213A1 (en) * | 2000-05-19 | 2002-01-17 | Robert Falotico | Drug/drug delivery systems for the prevention and treatment of vascular disease |
US6776796B2 (en) * | 2000-05-12 | 2004-08-17 | Cordis Corportation | Antiinflammatory drug and delivery device |
US20020005206A1 (en) * | 2000-05-19 | 2002-01-17 | Robert Falotico | Antiproliferative drug and delivery device |
US20020007215A1 (en) * | 2000-05-19 | 2002-01-17 | Robert Falotico | Drug/drug delivery systems for the prevention and treatment of vascular disease |
US20020007214A1 (en) * | 2000-05-19 | 2002-01-17 | Robert Falotico | Drug/drug delivery systems for the prevention and treatment of vascular disease |
US6673385B1 (en) * | 2000-05-31 | 2004-01-06 | Advanced Cardiovascular Systems, Inc. | Methods for polymeric coatings stents |
US6555157B1 (en) * | 2000-07-25 | 2003-04-29 | Advanced Cardiovascular Systems, Inc. | Method for coating an implantable device and system for performing the method |
US6503538B1 (en) * | 2000-08-30 | 2003-01-07 | Cornell Research Foundation, Inc. | Elastomeric functional biodegradable copolyester amides and copolyester urethanes |
US6716444B1 (en) * | 2000-09-28 | 2004-04-06 | Advanced Cardiovascular Systems, Inc. | Barriers for polymer-coated implantable medical devices and methods for making the same |
US6506437B1 (en) * | 2000-10-17 | 2003-01-14 | Advanced Cardiovascular Systems, Inc. | Methods of coating an implantable device having depots formed in a surface thereof |
US6544543B1 (en) * | 2000-12-27 | 2003-04-08 | Advanced Cardiovascular Systems, Inc. | Periodic constriction of vessels to treat ischemic tissue |
US6540776B2 (en) * | 2000-12-28 | 2003-04-01 | Advanced Cardiovascular Systems, Inc. | Sheath for a prosthesis and methods of forming the same |
US6544582B1 (en) * | 2001-01-05 | 2003-04-08 | Advanced Cardiovascular Systems, Inc. | Method and apparatus for coating an implantable device |
US6544223B1 (en) * | 2001-01-05 | 2003-04-08 | Advanced Cardiovascular Systems, Inc. | Balloon catheter for delivering therapeutic agents |
US20030032767A1 (en) * | 2001-02-05 | 2003-02-13 | Yasuhiro Tada | High-strength polyester-amide fiber and process for producing the same |
US20030004141A1 (en) * | 2001-03-08 | 2003-01-02 | Brown David L. | Medical devices, compositions and methods for treating vulnerable plaque |
US6712845B2 (en) * | 2001-04-24 | 2004-03-30 | Advanced Cardiovascular Systems, Inc. | Coating for a stent and a method of forming the same |
US6695920B1 (en) * | 2001-06-27 | 2004-02-24 | Advanced Cardiovascular Systems, Inc. | Mandrel for supporting a stent and a method of using the mandrel to coat a stent |
US6673154B1 (en) * | 2001-06-28 | 2004-01-06 | Advanced Cardiovascular Systems, Inc. | Stent mounting device to coat a stent |
US6706013B1 (en) * | 2001-06-29 | 2004-03-16 | Advanced Cardiovascular Systems, Inc. | Variable length drug delivery catheter |
US6527863B1 (en) * | 2001-06-29 | 2003-03-04 | Advanced Cardiovascular Systems, Inc. | Support device for a stent and a method of using the same to coat a stent |
US7195640B2 (en) * | 2001-09-25 | 2007-03-27 | Cordis Corporation | Coated medical devices for the treatment of vulnerable plaque |
US20030059520A1 (en) * | 2001-09-27 | 2003-03-27 | Yung-Ming Chen | Apparatus for regulating temperature of a composition and a method of coating implantable devices |
US20030065377A1 (en) * | 2001-09-28 | 2003-04-03 | Davila Luis A. | Coated medical devices |
US20030073961A1 (en) * | 2001-09-28 | 2003-04-17 | Happ Dorrie M. | Medical device containing light-protected therapeutic agent and a method for fabricating thereof |
US6709514B1 (en) * | 2001-12-28 | 2004-03-23 | Advanced Cardiovascular Systems, Inc. | Rotary coating apparatus for coating implantable medical devices |
-
2002
- 2002-04-05 US US10/117,650 patent/US7056967B2/en not_active Expired - Lifetime
- 2002-04-05 SK SK470-2002A patent/SK287686B6/sk not_active IP Right Cessation
- 2002-04-08 CZ CZ2002-1236A patent/CZ305019B6/cs not_active IP Right Cessation
- 2002-04-08 NO NO20021657A patent/NO333375B1/no not_active IP Right Cessation
- 2002-04-08 TW TW091106946A patent/TWI239019B/zh not_active IP Right Cessation
- 2002-04-08 AR ARP020101284A patent/AR033211A1/es active IP Right Grant
- 2002-04-09 JP JP2002106732A patent/JP4051667B2/ja not_active Expired - Lifetime
- 2002-04-09 CN CNB021060223A patent/CN1250636C/zh not_active Expired - Lifetime
- 2002-04-09 MY MYPI20021283A patent/MY133253A/en unknown
- 2002-04-09 KR KR1020020019147A patent/KR100923284B1/ko active IP Right Grant
- 2002-04-09 CA CA2380987A patent/CA2380987C/en not_active Expired - Lifetime
- 2002-04-09 AU AU32998/02A patent/AU784703B2/en not_active Expired
- 2002-04-09 SG SG200202081A patent/SG103854A1/en unknown
- 2002-04-10 MX MXPA02003611A patent/MXPA02003611A/es active IP Right Grant
- 2002-04-10 BR BRPI0201173-5A patent/BR0201173B1/pt not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
CZ305019B6 (cs) | 2015-04-01 |
CN1250636C (zh) | 2006-04-12 |
KR100923284B1 (ko) | 2009-10-23 |
CA2380987C (en) | 2011-03-15 |
BR0201173B1 (pt) | 2012-01-10 |
AU3299802A (en) | 2002-10-17 |
BR0201173A (pt) | 2003-06-10 |
AR033211A1 (es) | 2003-12-10 |
SK4702002A3 (en) | 2002-11-06 |
MXPA02003611A (es) | 2002-11-07 |
CN1381522A (zh) | 2002-11-27 |
SK287686B6 (sk) | 2011-06-06 |
MY133253A (en) | 2007-10-31 |
US20020198344A1 (en) | 2002-12-26 |
US7056967B2 (en) | 2006-06-06 |
KR20020079525A (ko) | 2002-10-19 |
JP4051667B2 (ja) | 2008-02-27 |
NO20021657D0 (no) | 2002-04-08 |
CZ20021236A3 (cs) | 2002-11-13 |
AU784703B2 (en) | 2006-06-01 |
TWI239019B (en) | 2005-09-01 |
NO20021657L (no) | 2002-10-11 |
CA2380987A1 (en) | 2002-10-10 |
JP2002363351A (ja) | 2002-12-18 |
SG103854A1 (en) | 2004-05-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
NO333375B1 (no) | Stabilisert isolasjonssammensetning for en mellom- og hoyspenningskabel | |
JP6598793B2 (ja) | N,n,n’,n’,n’’,n’’−ヘキサアリル−1,3,5−トリアジン−2,4,6−トリアミン架橋助剤を有する架橋性ポリマー組成物、それを作製するための方法、及びそれから作製された物品 | |
EP0296355B1 (en) | Water treeing/resistant compositions | |
US7452933B2 (en) | Cross-linked polyethylene having excellent inhibition of sweat-out and insulation properties | |
KR100727207B1 (ko) | 스웨트-아웃 억제 및 전기 절연특성이 우수한 가교 폴리에틸렌 조성물 | |
JP6599353B2 (ja) | ジアリルイソシアヌレート架橋助剤を有する架橋性ポリマー組成物、それを作製するための方法、及びそれから作製された物品 | |
KR102617022B1 (ko) | 메틸-라디칼 스캐빈저를 갖는 가교결합성 중합체 조성물 및 이로부터 제조된 물품 | |
JP6598794B2 (ja) | ジアリルアミド架橋助剤を有する架橋性ポリマー組成物、それを作製するための方法、及びそれから作製された物品 | |
EP1249845B1 (en) | Stabilized medium and high voltage cable insulation composition | |
JPH0662817B2 (ja) | 優れた耐熱老化性を有するvldpe基材組成物 | |
RU2318843C2 (ru) | Стабилизированный материал и композиции для высоковольтной изоляции кабеля | |
US20040242781A1 (en) | Elastomeric composition for the insulation of electric cables | |
JPH0114932B2 (zh) | ||
CN113383038A (zh) | 可湿固化聚烯烃调配物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MK1K | Patent expired |