NO332804B1 - Polymersammensetninger som omfatter telomerer som har tallmidlere telomeriseringsgrad pa mindre enn eller lik 8 og artikler eller artikkeldeler fremstilt ved anvendelse av disse sammensetningene - Google Patents
Polymersammensetninger som omfatter telomerer som har tallmidlere telomeriseringsgrad pa mindre enn eller lik 8 og artikler eller artikkeldeler fremstilt ved anvendelse av disse sammensetningene Download PDFInfo
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- NO332804B1 NO332804B1 NO20033265A NO20033265A NO332804B1 NO 332804 B1 NO332804 B1 NO 332804B1 NO 20033265 A NO20033265 A NO 20033265A NO 20033265 A NO20033265 A NO 20033265A NO 332804 B1 NO332804 B1 NO 332804B1
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- BSVQJWUUZCXSOL-UHFFFAOYSA-N cyclohexylsulfonyl ethaneperoxoate Chemical compound CC(=O)OOS(=O)(=O)C1CCCCC1 BSVQJWUUZCXSOL-UHFFFAOYSA-N 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
- KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- SJMLNDPIJZBEKY-UHFFFAOYSA-N ethyl 2,2,2-trichloroacetate Chemical compound CCOC(=O)C(Cl)(Cl)Cl SJMLNDPIJZBEKY-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-L fumarate(2-) Chemical class [O-]C(=O)\C=C\C([O-])=O VZCYOOQTPOCHFL-OWOJBTEDSA-L 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 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
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N itaconic acid Chemical class OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000013521 mastic Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000001455 metallic ions Chemical class 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical class CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- DUVTXUGBACWHBP-UHFFFAOYSA-N methyl 2-(1h-benzimidazol-2-ylmethoxy)benzoate Chemical compound COC(=O)C1=CC=CC=C1OCC1=NC2=CC=CC=C2N1 DUVTXUGBACWHBP-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 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
- 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
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000012436 odor-modifying agent Substances 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- UDKSLGIUCGAZTK-UHFFFAOYSA-N phenyl pentadecane-1-sulfonate Chemical compound CCCCCCCCCCCCCCCS(=O)(=O)OC1=CC=CC=C1 UDKSLGIUCGAZTK-UHFFFAOYSA-N 0.000 description 1
- JQCXWCOOWVGKMT-UHFFFAOYSA-N phthalic acid diheptyl ester Natural products CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC JQCXWCOOWVGKMT-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- LLLCSBYSPJHDJX-UHFFFAOYSA-M potassium;2-methylprop-2-enoate Chemical compound [K+].CC(=C)C([O-])=O LLLCSBYSPJHDJX-UHFFFAOYSA-M 0.000 description 1
- 229940088417 precipitated calcium carbonate Drugs 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229940047670 sodium acrylate Drugs 0.000 description 1
- VYGBQXDNOUHIBZ-UHFFFAOYSA-L sodium formaldehyde sulphoxylate Chemical compound [Na+].[Na+].O=C.[O-]S[O-] VYGBQXDNOUHIBZ-UHFFFAOYSA-L 0.000 description 1
- SONHXMAHPHADTF-UHFFFAOYSA-M sodium;2-methylprop-2-enoate Chemical compound [Na+].CC(=C)C([O-])=O SONHXMAHPHADTF-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate group Chemical group S(=O)(=O)([O-])[O-] QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- KQYLUTYUZIVHND-UHFFFAOYSA-N tert-butyl 2,2-dimethyloctaneperoxoate Chemical compound CCCCCCC(C)(C)C(=O)OOC(C)(C)C KQYLUTYUZIVHND-UHFFFAOYSA-N 0.000 description 1
- PZTAGFCBNDBBFZ-UHFFFAOYSA-N tert-butyl 2-(hydroxymethyl)piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCCCC1CO PZTAGFCBNDBBFZ-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
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 125000005591 trimellitate group Chemical group 0.000 description 1
- 238000013022 venting Methods 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- 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
-
- 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
- C08K5/10—Esters; Ether-esters
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0100778A FR2819816B1 (fr) | 2001-01-19 | 2001-01-19 | Compositions de polymeres comprenant des telomeres qui ont un degre de telomerisation moyen en nombre inferieur ou egal a 8 et articles ou parties d'articles fabriques en utilisant ces compositions |
| PCT/EP2002/000505 WO2002057351A1 (fr) | 2001-01-19 | 2002-01-16 | Compositions polymeres comprenant des telomeres et des articles ou parties d'articles fabriques a l'aide de ces compositions |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20033265D0 NO20033265D0 (no) | 2003-07-18 |
| NO20033265L NO20033265L (no) | 2003-09-16 |
| NO332804B1 true NO332804B1 (no) | 2013-01-14 |
Family
ID=8859057
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20033265A NO332804B1 (no) | 2001-01-19 | 2003-07-18 | Polymersammensetninger som omfatter telomerer som har tallmidlere telomeriseringsgrad pa mindre enn eller lik 8 og artikler eller artikkeldeler fremstilt ved anvendelse av disse sammensetningene |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US7019068B2 (fr) |
| EP (1) | EP1368422B1 (fr) |
| JP (1) | JP2004520464A (fr) |
| KR (1) | KR100854013B1 (fr) |
| CN (1) | CN1279096C (fr) |
| AT (1) | ATE302815T1 (fr) |
| BR (1) | BR0206592B1 (fr) |
| CA (1) | CA2434785C (fr) |
| CZ (1) | CZ297772B6 (fr) |
| DE (1) | DE60205726T2 (fr) |
| DK (1) | DK1368422T3 (fr) |
| ES (1) | ES2248530T3 (fr) |
| FR (1) | FR2819816B1 (fr) |
| MX (1) | MXPA03006459A (fr) |
| NO (1) | NO332804B1 (fr) |
| PL (1) | PL210648B1 (fr) |
| SI (1) | SI1368422T1 (fr) |
| WO (1) | WO2002057351A1 (fr) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7741524B2 (en) * | 2003-04-22 | 2010-06-22 | Solvay (Societe Anonyme) | Iodinated organic substances of low molecular mass and process for preparing them |
| WO2005028557A1 (fr) * | 2003-09-23 | 2005-03-31 | Solvay (Société Anonyme) | Composition polymere |
| US8372912B2 (en) | 2005-08-12 | 2013-02-12 | Eastman Chemical Company | Polyvinyl chloride compositions |
| EP2057243B1 (fr) * | 2006-08-30 | 2013-01-23 | Eastman Chemical Company | Compositions d'agent d'étanchéité comprenant un nouveau plastifiant |
| CN102850968B (zh) * | 2006-08-30 | 2015-09-09 | 伊士曼化工公司 | 乙酸乙烯酯聚合物组合物中作为增塑剂的对苯二甲酸酯 |
| CN101993548A (zh) * | 2010-09-30 | 2011-03-30 | 浙江嘉澳环保科技股份有限公司 | 一种环保复合型增塑剂及制备方法 |
| MX341216B (es) * | 2011-09-30 | 2016-08-11 | Dow Global Technologies Llc | Proceso para mezclar cloruro de polivinilo con un plastificador de base biologica. |
| KR101784100B1 (ko) * | 2015-04-06 | 2017-10-10 | 주식회사 엘지화학 | 가소제 조성물, 수지 조성물 및 이들의 제조 방법 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2820772A (en) * | 1953-12-30 | 1958-01-21 | Minnesota Mining & Mfg | Halogenated olefin polymers plasticized with a telomer containing perfluorochloroolefin monomer units and method of preparing same |
| US3022261A (en) * | 1954-06-25 | 1962-02-20 | Monsanto Chemicals | Vinyl resin plasticized with an adduct of an alkyl vinylphosphonate |
| US3173888A (en) * | 1962-11-13 | 1965-03-16 | Eastman Kodak Co | Diesters of diglycolic acid and vinyl chloride polymers plasticized therewith |
| FR1469454A (fr) * | 1963-02-11 | 1967-02-17 | Rohm & Haas | Compositions résineuses contenant des oligoesters |
| FR1441248A (fr) * | 1964-07-31 | 1966-06-03 | Air Reduction | Procédé de fabrication de télomères d'esters vinyliques |
| US3655589A (en) * | 1969-03-27 | 1972-04-11 | Bayer Ag | Flameproofed organic synthetic resins |
| US5071895A (en) * | 1990-01-18 | 1991-12-10 | Rohm And Haas Company | Functionally terminated acrylic acid telomers |
-
2001
- 2001-01-19 FR FR0100778A patent/FR2819816B1/fr not_active Expired - Fee Related
-
2002
- 2002-01-16 SI SI200230219T patent/SI1368422T1/sl unknown
- 2002-01-16 BR BRPI0206592-4A patent/BR0206592B1/pt not_active IP Right Cessation
- 2002-01-16 MX MXPA03006459A patent/MXPA03006459A/es active IP Right Grant
- 2002-01-16 CA CA002434785A patent/CA2434785C/fr not_active Expired - Fee Related
- 2002-01-16 PL PL367281A patent/PL210648B1/pl not_active IP Right Cessation
- 2002-01-16 AT AT02714091T patent/ATE302815T1/de active
- 2002-01-16 JP JP2002558419A patent/JP2004520464A/ja active Pending
- 2002-01-16 CN CNB028067681A patent/CN1279096C/zh not_active Expired - Fee Related
- 2002-01-16 ES ES02714091T patent/ES2248530T3/es not_active Expired - Lifetime
- 2002-01-16 EP EP02714091A patent/EP1368422B1/fr not_active Expired - Lifetime
- 2002-01-16 US US10/466,105 patent/US7019068B2/en not_active Expired - Fee Related
- 2002-01-16 DK DK02714091T patent/DK1368422T3/da active
- 2002-01-16 KR KR1020037009547A patent/KR100854013B1/ko not_active IP Right Cessation
- 2002-01-16 CZ CZ20031966A patent/CZ297772B6/cs not_active IP Right Cessation
- 2002-01-16 DE DE60205726T patent/DE60205726T2/de not_active Expired - Lifetime
- 2002-01-16 WO PCT/EP2002/000505 patent/WO2002057351A1/fr active IP Right Grant
-
2003
- 2003-07-18 NO NO20033265A patent/NO332804B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE60205726T2 (de) | 2006-06-22 |
| ATE302815T1 (de) | 2005-09-15 |
| CN1279096C (zh) | 2006-10-11 |
| SI1368422T1 (sl) | 2006-02-28 |
| MXPA03006459A (es) | 2004-02-12 |
| CA2434785A1 (fr) | 2002-07-25 |
| CZ297772B6 (cs) | 2007-03-28 |
| PL210648B1 (pl) | 2012-02-29 |
| US20040097625A1 (en) | 2004-05-20 |
| FR2819816B1 (fr) | 2003-04-11 |
| BR0206592A (pt) | 2004-02-17 |
| NO20033265L (no) | 2003-09-16 |
| EP1368422B1 (fr) | 2005-08-24 |
| WO2002057351A1 (fr) | 2002-07-25 |
| JP2004520464A (ja) | 2004-07-08 |
| DK1368422T3 (da) | 2006-01-09 |
| ES2248530T3 (es) | 2006-03-16 |
| NO20033265D0 (no) | 2003-07-18 |
| CZ20031966A3 (cs) | 2003-12-17 |
| KR20030077581A (ko) | 2003-10-01 |
| CA2434785C (fr) | 2009-04-07 |
| CN1498246A (zh) | 2004-05-19 |
| KR100854013B1 (ko) | 2008-08-26 |
| PL367281A1 (en) | 2005-02-21 |
| EP1368422A1 (fr) | 2003-12-10 |
| FR2819816A1 (fr) | 2002-07-26 |
| BR0206592B1 (pt) | 2011-06-28 |
| US7019068B2 (en) | 2006-03-28 |
| DE60205726D1 (de) | 2005-09-29 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM1K | Lapsed by not paying the annual fees |