NO801543L - Komposisjoner av organotrinn - stabilisatorer for vinylhalogen-harpikser. - Google Patents
Komposisjoner av organotrinn - stabilisatorer for vinylhalogen-harpikser.Info
- Publication number
- NO801543L NO801543L NO801543A NO801543A NO801543L NO 801543 L NO801543 L NO 801543L NO 801543 A NO801543 A NO 801543A NO 801543 A NO801543 A NO 801543A NO 801543 L NO801543 L NO 801543L
- Authority
- NO
- Norway
- Prior art keywords
- compounds
- mixture
- organotin
- tin
- stabilizers
- Prior art date
Links
- -1 VINYL HALOGEN Chemical class 0.000 title claims description 18
- 239000000203 mixture Substances 0.000 title claims description 14
- 239000003381 stabilizer Substances 0.000 title claims description 13
- 229920002554 vinyl polymer Polymers 0.000 title claims description 5
- 229920005989 resin Polymers 0.000 title description 9
- 239000011347 resin Substances 0.000 title description 9
- 229910052736 halogen Inorganic materials 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 12
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 8
- 239000004800 polyvinyl chloride Substances 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 claims description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 3
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
- 125000003158 alcohol group Chemical group 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 150000001336 alkenes Chemical class 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 125000005358 mercaptoalkyl group Chemical group 0.000 claims description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims description 2
- 150000003606 tin compounds Chemical class 0.000 claims description 2
- DUXYWXYOBMKGIN-UHFFFAOYSA-N trimyristin Chemical compound CCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCC DUXYWXYOBMKGIN-UHFFFAOYSA-N 0.000 claims 2
- KKZDAVJPUYTNHE-UHFFFAOYSA-L 2-(6-methylheptylsulfanyl)acetate tin(2+) Chemical compound [Sn+2].C(CCCCC(C)C)SCC(=O)[O-].C(CCCCC(C)C)SCC(=O)[O-] KKZDAVJPUYTNHE-UHFFFAOYSA-L 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims 1
- 229920001291 polyvinyl halide Polymers 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 230000006641 stabilisation Effects 0.000 claims 1
- 238000011105 stabilization Methods 0.000 claims 1
- 238000009472 formulation Methods 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 238000002845 discoloration Methods 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000007983 Tris buffer Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 230000000087 stabilizing effect Effects 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 2
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- JNHUZSVMIPOGQO-UHFFFAOYSA-N 2-sulfanylethyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCS JNHUZSVMIPOGQO-UHFFFAOYSA-N 0.000 description 1
- FPRWILGFWFTOHA-UHFFFAOYSA-N 2-sulfanylethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCS FPRWILGFWFTOHA-UHFFFAOYSA-N 0.000 description 1
- BNZMFBWZRAWMQT-UHFFFAOYSA-N 2-sulfanylethyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCCS BNZMFBWZRAWMQT-UHFFFAOYSA-N 0.000 description 1
- YWSBAZUYMJQRRQ-UHFFFAOYSA-M CCCCCCCCCCCCCCCCCC(=O)OCCS[Sn] Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCS[Sn] YWSBAZUYMJQRRQ-UHFFFAOYSA-M 0.000 description 1
- QBCZEPUQKQTKQL-UHFFFAOYSA-K Cl[Sn](CCCC(=O)OC)(Cl)Cl Chemical compound Cl[Sn](CCCC(=O)OC)(Cl)Cl QBCZEPUQKQTKQL-UHFFFAOYSA-K 0.000 description 1
- 239000004605 External Lubricant Substances 0.000 description 1
- FCSHMCFRCYZTRQ-UHFFFAOYSA-N N,N'-diphenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)NC1=CC=CC=C1 FCSHMCFRCYZTRQ-UHFFFAOYSA-N 0.000 description 1
- 241000208181 Pelargonium Species 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- YSCDKUPSJMMGGT-UHFFFAOYSA-L [dibutyl-[2-(6-methylheptylsulfanyl)acetyl]oxystannyl] 2-(6-methylheptylsulfanyl)acetate Chemical compound CC(C)CCCCCSCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CSCCCCCC(C)C YSCDKUPSJMMGGT-UHFFFAOYSA-L 0.000 description 1
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 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
- 150000002367 halogens Chemical class 0.000 description 1
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 238000009428 plumbing Methods 0.000 description 1
- 229920002493 poly(chlorotrifluoroethylene) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 239000005023 polychlorotrifluoroethylene (PCTFE) polymer Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Chemical group 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
- 239000002904 solvent Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/226—Compounds with one or more Sn-S linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7913109A FR2457298A1 (fr) | 1979-05-23 | 1979-05-23 | Compositions de stabilisants organostanniques pour resines halogeno-vinyliques |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO801543L true NO801543L (no) | 1980-11-24 |
Family
ID=9225766
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO801543A NO801543L (no) | 1979-05-23 | 1980-05-22 | Komposisjoner av organotrinn - stabilisatorer for vinylhalogen-harpikser. |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US4329279A (el) |
| EP (1) | EP0021033B2 (el) |
| JP (1) | JPS55157639A (el) |
| AU (1) | AU536523B2 (el) |
| BR (1) | BR8003214A (el) |
| CA (1) | CA1139309A (el) |
| DE (1) | DE3061996D1 (el) |
| DK (1) | DK224080A (el) |
| ES (1) | ES8200114A1 (el) |
| FI (1) | FI801645A (el) |
| FR (1) | FR2457298A1 (el) |
| GR (1) | GR68429B (el) |
| IE (1) | IE49818B1 (el) |
| IL (1) | IL60143A (el) |
| IN (1) | IN154328B (el) |
| NO (1) | NO801543L (el) |
| PT (1) | PT71268A (el) |
| YU (1) | YU136280A (el) |
| ZA (1) | ZA803047B (el) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5744215A (en) | 1996-01-04 | 1998-04-28 | Ppg Industries, Inc. | Reduction of haze in transparent coatings |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL91173C (el) * | 1900-01-01 | |||
| CH341992A (de) * | 1953-07-24 | 1959-10-31 | Metal & Thermit Corp | Verfahren zur Verbesserung der Hitze- und Lichtbeständigkeit von halogenhaltigen Harzen |
| NL7412230A (nl) * | 1974-09-16 | 1976-03-18 | Akzo Nv | Werkwijze voor de bereiding van organotintri- halogeniden. |
| US4105684A (en) * | 1974-09-16 | 1978-08-08 | Akzo N.V. | Process for the preparation of organotin trihalides |
| NL7503116A (nl) * | 1975-03-17 | 1976-09-21 | Akzo Nv | Werkwijze voor het bereiden van organotindihaloge- niden, alsmede daarvan afgeleide organotinstabi- lisatoren. |
| US4080363A (en) * | 1975-03-17 | 1978-03-21 | Akzo N.V. | Process for making organotin dihalides and trihalides and stabilizers prepared therefrom |
| US4167520A (en) * | 1976-01-23 | 1979-09-11 | Akzo N.V. | Process for preparing organotin trihalides |
| US4124618A (en) * | 1976-11-02 | 1978-11-07 | M&T Chemicals Inc. | Method for preparing bis(organotin mercaptoalkanol ester) sulfides |
| US4104292A (en) * | 1976-11-02 | 1978-08-01 | M&T Chemicals Inc. | Method for preparing organotin compounds |
| DE2735810B2 (de) * | 1977-08-09 | 1981-01-29 | Hoechst Ag, 6000 Frankfurt | Gemische aus Organozinnverbindungen und ihre Verwendung als Stabilisatoren für chlorhaltige Polymere |
| DE2860601D1 (en) * | 1977-09-09 | 1981-04-30 | Ciba Geigy Ag | Organotin compounds, process for their preparation and their use as intermediate products for stabilisers |
| NL7712313A (nl) * | 1977-11-09 | 1979-05-11 | Akzo Nv | Werkwijze ter bereiding van organotin verbin- dingen. |
-
1979
- 1979-05-23 FR FR7913109A patent/FR2457298A1/fr active Granted
-
1980
- 1980-05-19 IN IN363/DEL/80A patent/IN154328B/en unknown
- 1980-05-20 DE DE8080102794T patent/DE3061996D1/de not_active Expired
- 1980-05-20 EP EP80102794A patent/EP0021033B2/fr not_active Expired
- 1980-05-20 PT PT71268A patent/PT71268A/pt unknown
- 1980-05-20 US US06/151,638 patent/US4329279A/en not_active Expired - Lifetime
- 1980-05-21 FI FI801645A patent/FI801645A/fi not_active Application Discontinuation
- 1980-05-21 YU YU01362/80A patent/YU136280A/xx unknown
- 1980-05-21 AU AU58632/80A patent/AU536523B2/en not_active Ceased
- 1980-05-22 ZA ZA00803047A patent/ZA803047B/xx unknown
- 1980-05-22 IL IL60143A patent/IL60143A/xx unknown
- 1980-05-22 IE IE1075/80A patent/IE49818B1/en unknown
- 1980-05-22 ES ES491739A patent/ES8200114A1/es not_active Expired
- 1980-05-22 CA CA000352526A patent/CA1139309A/fr not_active Expired
- 1980-05-22 BR BR8003214A patent/BR8003214A/pt unknown
- 1980-05-22 JP JP6718880A patent/JPS55157639A/ja active Granted
- 1980-05-22 DK DK224080A patent/DK224080A/da unknown
- 1980-05-22 NO NO801543A patent/NO801543L/no unknown
- 1980-05-22 GR GR62027A patent/GR68429B/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0021033A1 (fr) | 1981-01-07 |
| CA1139309A (fr) | 1983-01-11 |
| GR68429B (el) | 1981-12-30 |
| IE801075L (en) | 1980-11-23 |
| AU536523B2 (en) | 1984-05-10 |
| EP0021033B2 (fr) | 1987-10-21 |
| IN154328B (el) | 1984-10-20 |
| DE3061996D1 (en) | 1983-03-24 |
| IL60143A (en) | 1986-03-31 |
| AU5863280A (en) | 1980-09-25 |
| US4329279A (en) | 1982-05-11 |
| FR2457298B1 (el) | 1982-07-02 |
| ES491739A0 (es) | 1981-10-16 |
| FI801645A (fi) | 1980-11-24 |
| JPH0153296B2 (el) | 1989-11-13 |
| JPS55157639A (en) | 1980-12-08 |
| BR8003214A (pt) | 1980-12-30 |
| IL60143A0 (en) | 1980-07-31 |
| FR2457298A1 (fr) | 1980-12-19 |
| EP0021033B1 (fr) | 1983-02-16 |
| DK224080A (da) | 1980-11-24 |
| PT71268A (fr) | 1980-06-01 |
| ZA803047B (en) | 1981-05-27 |
| IE49818B1 (en) | 1985-12-25 |
| ES8200114A1 (es) | 1981-10-16 |
| YU136280A (en) | 1983-09-30 |
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