ZA200706627B - Process for preparing crosslinked polymers - Google Patents
Process for preparing crosslinked polymers Download PDFInfo
- Publication number
- ZA200706627B ZA200706627B ZA200706627A ZA200706627A ZA200706627B ZA 200706627 B ZA200706627 B ZA 200706627B ZA 200706627 A ZA200706627 A ZA 200706627A ZA 200706627 A ZA200706627 A ZA 200706627A ZA 200706627 B ZA200706627 B ZA 200706627B
- Authority
- ZA
- South Africa
- Prior art keywords
- process according
- unsaturated polyolefin
- crosslinking agent
- blend
- crosslinking
- Prior art date
Links
- 229920006037 cross link polymer Polymers 0.000 title claims abstract description 12
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 9
- 239000000203 mixture Substances 0.000 claims abstract description 82
- 229920000098 polyolefin Polymers 0.000 claims abstract description 66
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 49
- 238000004132 cross linking Methods 0.000 claims abstract description 43
- 238000002156 mixing Methods 0.000 claims abstract description 30
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 24
- 239000007788 liquid Substances 0.000 claims abstract description 24
- 238000001125 extrusion Methods 0.000 claims abstract description 17
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims abstract description 10
- 239000000758 substrate Substances 0.000 claims abstract description 5
- 238000000034 method Methods 0.000 claims description 47
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 31
- 239000000654 additive Substances 0.000 claims description 28
- 239000003963 antioxidant agent Substances 0.000 claims description 28
- 150000002978 peroxides Chemical class 0.000 claims description 23
- 230000003078 antioxidant effect Effects 0.000 claims description 22
- -1 siloxanes Chemical group 0.000 claims description 18
- 230000000996 additive effect Effects 0.000 claims description 13
- 239000004698 Polyethylene Substances 0.000 claims description 11
- 229920000573 polyethylene Polymers 0.000 claims description 11
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 8
- 239000005977 Ethylene Substances 0.000 claims description 8
- 239000000178 monomer Substances 0.000 claims description 7
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 7
- XWJBRBSPAODJER-UHFFFAOYSA-N 1,7-octadiene Chemical group C=CCCCCC=C XWJBRBSPAODJER-UHFFFAOYSA-N 0.000 claims description 6
- 150000001336 alkenes Chemical class 0.000 claims description 5
- 150000001993 dienes Chemical group 0.000 claims description 5
- 239000011247 coating layer Substances 0.000 claims description 3
- 239000004020 conductor Substances 0.000 claims description 3
- 239000003381 stabilizer Substances 0.000 claims description 3
- UCKITPBQPGXDHV-UHFFFAOYSA-N 7-methylocta-1,6-diene Chemical compound CC(C)=CCCCC=C UCKITPBQPGXDHV-UHFFFAOYSA-N 0.000 claims description 2
- PWENCKJTWWADRJ-UHFFFAOYSA-N 9-methyldeca-1,8-diene Chemical compound CC(C)=CCCCCCC=C PWENCKJTWWADRJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000006057 Non-nutritive feed additive Substances 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- NLDGJRWPPOSWLC-UHFFFAOYSA-N deca-1,9-diene Chemical compound C=CCCCCCCC=C NLDGJRWPPOSWLC-UHFFFAOYSA-N 0.000 claims description 2
- WGMIOQPQEKMMGM-UHFFFAOYSA-N dodeca-1,11-diene;tetradeca-1,13-diene Chemical compound C=CCCCCCCCCC=C.C=CCCCCCCCCCCC=C WGMIOQPQEKMMGM-UHFFFAOYSA-N 0.000 claims 1
- 125000002081 peroxide group Chemical group 0.000 claims 1
- 229920000642 polymer Polymers 0.000 description 42
- 239000008188 pellet Substances 0.000 description 16
- 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 13
- 230000000052 comparative effect Effects 0.000 description 8
- 239000000155 melt Substances 0.000 description 8
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 7
- 230000001965 increasing effect Effects 0.000 description 7
- 150000003254 radicals Chemical class 0.000 description 7
- 229920002554 vinyl polymer Polymers 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000000843 powder Substances 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 4
- 239000004594 Masterbatch (MB) Substances 0.000 description 4
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- ZOKCNEIWFQCSCM-UHFFFAOYSA-N (2-methyl-4-phenylpent-4-en-2-yl)benzene Chemical compound C=1C=CC=CC=1C(C)(C)CC(=C)C1=CC=CC=C1 ZOKCNEIWFQCSCM-UHFFFAOYSA-N 0.000 description 3
- KRDXTHSSNCTAGY-UHFFFAOYSA-N 2-cyclohexylpyrrolidine Chemical compound C1CCNC1C1CCCCC1 KRDXTHSSNCTAGY-UHFFFAOYSA-N 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 239000008240 homogeneous mixture Substances 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 239000011369 resultant mixture Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- CCNDOQHYOIISTA-UHFFFAOYSA-N 1,2-bis(2-tert-butylperoxypropan-2-yl)benzene Chemical compound CC(C)(C)OOC(C)(C)C1=CC=CC=C1C(C)(C)OOC(C)(C)C CCNDOQHYOIISTA-UHFFFAOYSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- SDJHPPZKZZWAKF-UHFFFAOYSA-N 2,3-dimethylbuta-1,3-diene Chemical compound CC(=C)C(C)=C SDJHPPZKZZWAKF-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 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 2
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000012986 chain transfer agent Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000011243 crosslinked material Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 239000011256 inorganic filler Substances 0.000 description 2
- 229910003475 inorganic filler Inorganic materials 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical group C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 150000003623 transition metal compounds Chemical class 0.000 description 2
- SOVOPSCRHKEUNJ-VQHVLOKHSA-N (e)-dec-4-ene Chemical compound CCCCC\C=C\CCC SOVOPSCRHKEUNJ-VQHVLOKHSA-N 0.000 description 1
- NALFRYPTRXKZPN-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane Chemical compound CC1CC(C)(C)CC(OOC(C)(C)C)(OOC(C)(C)C)C1 NALFRYPTRXKZPN-UHFFFAOYSA-N 0.000 description 1
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 1
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 1
- ODBCKCWTWALFKM-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhex-3-yne Chemical compound CC(C)(C)OOC(C)(C)C#CC(C)(C)OOC(C)(C)C ODBCKCWTWALFKM-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
- RCBGGJURENJHKV-UHFFFAOYSA-N 2-methylhept-1-ene Chemical compound CCCCCC(C)=C RCBGGJURENJHKV-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 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
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000002902 bimodal effect Effects 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000000071 blow moulding Methods 0.000 description 1
- 238000010504 bond cleavage reaction Methods 0.000 description 1
- BXIQXYOPGBXIEM-UHFFFAOYSA-N butyl 4,4-bis(tert-butylperoxy)pentanoate Chemical compound CCCCOC(=O)CCC(C)(OOC(C)(C)C)OOC(C)(C)C BXIQXYOPGBXIEM-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000012718 coordination polymerization Methods 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- IYPLTVKTLDQUGG-UHFFFAOYSA-N dodeca-1,11-diene Chemical compound C=CCCCCCCCCC=C IYPLTVKTLDQUGG-UHFFFAOYSA-N 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000006353 environmental stress Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 125000000687 hydroquinonyl group Chemical class C1(O)=C(C=C(O)C=C1)* 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 150000004059 quinone derivatives Chemical class 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 238000001175 rotational moulding Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 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
- XMRSTLBCBDIKFI-UHFFFAOYSA-N tetradeca-1,13-diene Chemical compound C=CCCCCCCCCCCC=C XMRSTLBCBDIKFI-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0025—Crosslinking or vulcanising agents; including accelerators
-
- 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
-
- 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
- C08L23/26—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment
-
- 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
- C08K5/14—Peroxides
-
- 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
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0807—Copolymers of ethene with unsaturated hydrocarbons only containing more than three carbon atoms
- C08L23/083—Copolymers of ethene with aliphatic polyenes, i.e. containing more than one unsaturated bond
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Processes Specially Adapted For Manufacturing Cables (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05004358A EP1695992B1 (en) | 2005-02-28 | 2005-02-28 | Process for preparing crosslinked polymers |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200706627B true ZA200706627B (en) | 2008-06-25 |
Family
ID=34933984
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200706627A ZA200706627B (en) | 2005-02-28 | 2007-08-08 | Process for preparing crosslinked polymers |
Country Status (18)
Country | Link |
---|---|
US (1) | US20080182935A1 (no) |
EP (1) | EP1695992B1 (no) |
JP (1) | JP2008531795A (no) |
KR (1) | KR100880998B1 (no) |
CN (1) | CN101128520B (no) |
AT (1) | ATE456607T1 (no) |
BR (1) | BRPI0607656B1 (no) |
CA (1) | CA2597772A1 (no) |
DE (1) | DE602005019132D1 (no) |
DK (1) | DK1695992T3 (no) |
EA (1) | EA014017B1 (no) |
ES (1) | ES2335894T3 (no) |
IL (1) | IL185098A0 (no) |
MX (1) | MX2007010222A (no) |
NO (1) | NO338467B1 (no) |
PL (1) | PL1695992T3 (no) |
WO (1) | WO2006089793A1 (no) |
ZA (1) | ZA200706627B (no) |
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---|---|---|---|---|
CA2644747C (en) * | 2006-03-24 | 2014-05-13 | Saudi Basic Industries Corporation | An extrusion coating composition |
EP1944327B2 (en) * | 2007-01-09 | 2018-11-28 | Borealis Technology Oy | A cross-linking agent |
CN101848947B (zh) * | 2007-11-06 | 2012-07-18 | 帝斯曼知识产权资产管理有限公司 | 用于制造(超)高分子量聚乙烯的方法 |
DE602007005503D1 (de) * | 2007-12-28 | 2010-05-06 | Borealis Tech Oy | Vernetzbares Gemisch zur Herstellung eines geschichteten Artikels |
US9058918B2 (en) | 2008-06-05 | 2015-06-16 | Union Carbide Chemicals & Plastics Technology Llc | Method for producing water tree-resistant, TRXLPE-type cable sheath |
US8722763B2 (en) | 2008-12-22 | 2014-05-13 | Borealis Ag | Masterbatch and process for preparing a polymer composition |
EP2256158B1 (en) | 2009-05-26 | 2014-07-02 | Borealis AG | Polymer composition for crosslinked articles |
EP2454076B1 (en) | 2009-06-22 | 2013-08-14 | Borealis AG | Chlorine dioxide resistant polyethylene pipes, their preparation and use |
ES2758129T3 (es) | 2009-11-11 | 2020-05-04 | Borealis Ag | Un cable y procedimiento de producción del mismo |
CN102666602B (zh) | 2009-11-11 | 2015-11-25 | 博瑞立斯有限公司 | 具有有利的电性能的可交联的聚合物组合物和电缆 |
JP5902094B2 (ja) | 2009-11-11 | 2016-04-13 | ボレアリス エージー | ポリマー組成物およびそれを含む電力ケーブル |
EA022362B1 (ru) | 2009-11-11 | 2015-12-30 | Бореалис Аг | Силовой кабель, способ его получения и применение полимерной композиции, содержащей полиолефин |
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CN102947384B (zh) | 2010-03-17 | 2016-08-10 | 北欧化工股份公司 | 具有优异电特性的适于电线电缆应用的聚和物组合物 |
EP2439234B1 (en) | 2010-10-07 | 2013-04-03 | Borealis AG | Polymer Composition |
EP3591670A1 (en) | 2010-11-03 | 2020-01-08 | Borealis AG | A polymer composition and a power cable comprising the polymer composition |
WO2012150285A1 (en) * | 2011-05-04 | 2012-11-08 | Borealis Ag | Polymer composition for electrical devices |
JP6428199B2 (ja) * | 2013-11-26 | 2018-11-28 | 日本ポリエチレン株式会社 | 太陽電池封止材用樹脂組成物、並びにそれを用いた太陽電池封止材及び太陽電池モジュール |
US11355260B2 (en) | 2013-12-19 | 2022-06-07 | Borealis Ag | Low MFR polymer composition, power cable insulation and power cable |
WO2015090639A1 (en) | 2013-12-19 | 2015-06-25 | Borealis Ag | A new polymer composition, power cable insulation and power cable |
EP3083796B1 (en) * | 2013-12-19 | 2019-05-22 | Borealis AG | A new crosslinked polymer composition, power cable insulation and power cable |
KR102448281B1 (ko) * | 2015-05-22 | 2022-09-29 | 다우 글로벌 테크놀로지스 엘엘씨 | 가교결합된 절연층으로 케이블을 제조하는 방법 및 상기 케이블 |
WO2019121716A1 (en) | 2017-12-18 | 2019-06-27 | Borealis Ag | Cable made from crosslinkable composition without antioxidant and with beneficial methane formation |
EP3728440B1 (en) * | 2017-12-18 | 2022-08-17 | Borealis AG | Polymer composition comprising a polyethylene |
EP3728441B1 (en) * | 2017-12-18 | 2023-03-01 | Borealis AG | Crosslinkable composition without antioxidant and beneficial methane formation with reduced crosslinking |
KR20200100737A (ko) * | 2017-12-18 | 2020-08-26 | 보레알리스 아게 | 산화방지제를 갖는 가교결합성 조성물 및 메탄 형성 및 제품 |
CN116063763A (zh) * | 2021-11-01 | 2023-05-05 | 中国石油化工股份有限公司 | 聚乙烯组合物和过氧化物交联聚乙烯管材 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS6019745B2 (ja) * | 1978-03-27 | 1985-05-17 | 三井化学株式会社 | ペルオキシド組成物、その製法、その用途 |
US4528155A (en) * | 1983-07-12 | 1985-07-09 | Alcan Aluminum Corporation | Production of cross-linked polymeric extruded articles |
JP2855875B2 (ja) * | 1990-04-16 | 1999-02-10 | 日本油脂株式会社 | エチレン系ポリマーの架橋可能な組成物及び架橋方法 |
JP2924087B2 (ja) * | 1990-05-24 | 1999-07-26 | 三菱化学株式会社 | ランダム共重合体の架橋体及び架橋発泡体 |
JPH04212208A (ja) * | 1990-09-13 | 1992-08-03 | Furukawa Electric Co Ltd:The | ゴム・プラスチック絶縁電力ケーブルとその接続部、ならびに、それらの製造方法 |
SE9103077D0 (sv) * | 1991-10-22 | 1991-10-22 | Neste Oy | Omaettad etensampolymer och saett foer framstaellning daerav |
JPH09306265A (ja) * | 1996-05-16 | 1997-11-28 | Nippon Unicar Co Ltd | 電力ケーブルおよびその製造方法 |
SE507045C2 (sv) * | 1996-05-31 | 1998-03-23 | Borealis As | Etensampolymer med förhöjd omättnadsgrad och sätt för framställning därav |
SE515111C2 (sv) * | 1998-10-23 | 2001-06-11 | Borealis As | Elektronisk kabel och sätt för framställning därav |
US6231978B1 (en) * | 1999-03-31 | 2001-05-15 | Union Carbide Chemicals & Plastics Technology Corporation | Crosslinkable polyethylene composition |
SE516260C2 (sv) * | 1999-07-01 | 2001-12-10 | Borealis Polymers Oy | Isolerande komposition för en elektrisk kraftkabel |
DE10060775A1 (de) * | 2000-12-07 | 2002-06-13 | Creavis Tech & Innovation Gmbh | Oligomere Silasesquioxane und Verfahren zur Herstellung von oligomeren Silasesquioxanen |
DE602005008366D1 (de) * | 2005-02-28 | 2008-09-04 | Borealis Tech Oy | Versengungshemmende Polymerzusammensetzung |
-
2005
- 2005-02-28 DE DE602005019132T patent/DE602005019132D1/de active Active
- 2005-02-28 PL PL05004358T patent/PL1695992T3/pl unknown
- 2005-02-28 EP EP05004358A patent/EP1695992B1/en active Active
- 2005-02-28 ES ES05004358T patent/ES2335894T3/es active Active
- 2005-02-28 DK DK05004358.7T patent/DK1695992T3/da active
- 2005-02-28 AT AT05004358T patent/ATE456607T1/de not_active IP Right Cessation
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2006
- 2006-02-27 KR KR1020077022351A patent/KR100880998B1/ko active IP Right Grant
- 2006-02-27 MX MX2007010222A patent/MX2007010222A/es unknown
- 2006-02-27 WO PCT/EP2006/001793 patent/WO2006089793A1/en not_active Application Discontinuation
- 2006-02-27 JP JP2007557402A patent/JP2008531795A/ja active Pending
- 2006-02-27 CN CN2006800062533A patent/CN101128520B/zh active Active
- 2006-02-27 CA CA002597772A patent/CA2597772A1/en not_active Abandoned
- 2006-02-27 EA EA200701561A patent/EA014017B1/ru not_active IP Right Cessation
- 2006-02-27 US US11/885,141 patent/US20080182935A1/en not_active Abandoned
- 2006-02-27 BR BRPI0607656-4A patent/BRPI0607656B1/pt active IP Right Grant
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2007
- 2007-08-07 IL IL185098A patent/IL185098A0/en unknown
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Also Published As
Publication number | Publication date |
---|---|
KR100880998B1 (ko) | 2009-02-03 |
IL185098A0 (en) | 2007-12-03 |
WO2006089793A1 (en) | 2006-08-31 |
CN101128520A (zh) | 2008-02-20 |
ES2335894T3 (es) | 2010-04-06 |
EA014017B1 (ru) | 2010-08-30 |
US20080182935A1 (en) | 2008-07-31 |
PL1695992T3 (pl) | 2010-07-30 |
EP1695992A1 (en) | 2006-08-30 |
NO20074099L (no) | 2007-09-04 |
DE602005019132D1 (de) | 2010-03-18 |
JP2008531795A (ja) | 2008-08-14 |
BRPI0607656B1 (pt) | 2017-07-04 |
DK1695992T3 (da) | 2010-05-10 |
NO338467B1 (no) | 2016-08-22 |
KR20070116840A (ko) | 2007-12-11 |
CN101128520B (zh) | 2012-01-18 |
CA2597772A1 (en) | 2006-08-31 |
EA200701561A1 (ru) | 2008-02-28 |
ATE456607T1 (de) | 2010-02-15 |
EP1695992B1 (en) | 2010-01-27 |
BRPI0607656A2 (pt) | 2009-09-22 |
MX2007010222A (es) | 2007-11-07 |
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