DE1669976A1 - Stabilisierte nicht- bzw. helleingefaerbte Polyamide - Google Patents
Stabilisierte nicht- bzw. helleingefaerbte PolyamideInfo
- Publication number
- DE1669976A1 DE1669976A1 DE19671669976 DE1669976A DE1669976A1 DE 1669976 A1 DE1669976 A1 DE 1669976A1 DE 19671669976 DE19671669976 DE 19671669976 DE 1669976 A DE1669976 A DE 1669976A DE 1669976 A1 DE1669976 A1 DE 1669976A1
- Authority
- DE
- Germany
- Prior art keywords
- colored
- carbon atoms
- chain
- straight
- addition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000004952 Polyamide Substances 0.000 title claims description 8
- 229920002647 polyamide Polymers 0.000 title claims description 8
- 150000002989 phenols Chemical class 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- -1 aliphatic alcohols Chemical class 0.000 claims description 6
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical class OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 6
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 3
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 125000004185 ester group Chemical group 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 125000004417 unsaturated alkyl group Chemical group 0.000 claims description 2
- 239000003381 stabilizer Substances 0.000 description 9
- 229910052724 xenon Inorganic materials 0.000 description 4
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 4
- 239000004327 boric acid Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 3
- 238000006068 polycondensation reaction Methods 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- ASLNDVUAZOHADR-UHFFFAOYSA-N 2-butyl-3-methylphenol Chemical compound CCCCC1=C(C)C=CC=C1O ASLNDVUAZOHADR-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- NMAKPIATXQEXBT-UHFFFAOYSA-N didecyl phenyl phosphite Chemical compound CCCCCCCCCCOP(OCCCCCCCCCC)OC1=CC=CC=C1 NMAKPIATXQEXBT-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- GPOGLVDBOFRHDV-UHFFFAOYSA-N (2-nonylphenyl) dihydrogen phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(O)O GPOGLVDBOFRHDV-UHFFFAOYSA-N 0.000 description 1
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- MQWCQFCZUNBTCM-UHFFFAOYSA-N 2-tert-butyl-6-(3-tert-butyl-2-hydroxy-5-methylphenyl)sulfanyl-4-methylphenol Chemical compound CC(C)(C)C1=CC(C)=CC(SC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O MQWCQFCZUNBTCM-UHFFFAOYSA-N 0.000 description 1
- ADRNSOYXKABLGT-UHFFFAOYSA-N 8-methylnonyl diphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OCCCCCCCC(C)C)OC1=CC=CC=C1 ADRNSOYXKABLGT-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- NOQGZXFMHARMLW-UHFFFAOYSA-N Daminozide Chemical compound CN(C)NC(=O)CCC(O)=O NOQGZXFMHARMLW-UHFFFAOYSA-N 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- BLXLSQIOCCHAHJ-UHFFFAOYSA-N [2,3,4-tri(nonyl)phenyl] dihydrogen phosphite Chemical compound CCCCCCCCCC1=CC=C(OP(O)O)C(CCCCCCCCC)=C1CCCCCCCCC BLXLSQIOCCHAHJ-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000006487 butyl benzyl group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000003857 carboxamides Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 125000005266 diarylamine group Chemical group 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002895 organic esters Chemical class 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 229920003987 resole Polymers 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- WAXLMVCEFHKADZ-UHFFFAOYSA-N tris-decyl borate Chemical compound CCCCCCCCCCOB(OCCCCCCCCCC)OCCCCCCCCCC WAXLMVCEFHKADZ-UHFFFAOYSA-N 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
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)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3585268A GB1180158A (en) | 1967-08-08 | 1968-07-26 | Stabilised Colourless or Light-Coloured Polyamides |
| FR1576859D FR1576859A (cs) | 1967-08-08 | 1968-08-07 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DED0053796 | 1967-08-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1669976A1 true DE1669976A1 (de) | 1971-08-26 |
Family
ID=7055256
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19671669976 Pending DE1669976A1 (de) | 1967-08-08 | 1967-08-08 | Stabilisierte nicht- bzw. helleingefaerbte Polyamide |
Country Status (7)
| Country | Link |
|---|---|
| AT (1) | AT283744B (cs) |
| BE (1) | BE718467A (cs) |
| CH (1) | CH503770A (cs) |
| DE (1) | DE1669976A1 (cs) |
| ES (1) | ES356519A1 (cs) |
| NL (1) | NL6810948A (cs) |
| SE (1) | SE332297B (cs) |
-
1967
- 1967-08-08 DE DE19671669976 patent/DE1669976A1/de active Pending
-
1968
- 1968-07-23 CH CH1102068A patent/CH503770A/de not_active IP Right Cessation
- 1968-07-24 BE BE718467D patent/BE718467A/xx unknown
- 1968-07-26 ES ES356519A patent/ES356519A1/es not_active Expired
- 1968-08-01 NL NL6810948A patent/NL6810948A/xx unknown
- 1968-08-07 AT AT773668A patent/AT283744B/de not_active IP Right Cessation
- 1968-08-07 SE SE1066768A patent/SE332297B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES356519A1 (es) | 1970-01-16 |
| AT283744B (de) | 1970-08-25 |
| NL6810948A (cs) | 1969-02-11 |
| SE332297B (cs) | 1971-02-01 |
| CH503770A (de) | 1971-02-28 |
| BE718467A (cs) | 1968-12-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE918778C (de) | Verfahren zur Herstellung von Polykondensationsprodukten | |
| DE1719223B2 (de) | Stabilisierte vinylhalogenidpolymerisat-formmasse | |
| CH501033A (de) | Verfahren zur Stabilisierung eines halogenhaltigen organischen Polymers | |
| DE1223541B (de) | Verfahren zum Stabilisieren von Polypropylen durch eine Phosphonsaeureester enthaltende Stabilisatormischung | |
| DE1231891B (de) | Verfahren zum Stabilisieren von Polymerisaten monoolefinisch ungesaettigter Kohlenwasserstoffe | |
| DE1669989A1 (de) | Verwendung von Stabilisatormischungen zur Stabilisierung von halogenhaltigen Polymerisatkunststoffmischungen | |
| DE1669976A1 (de) | Stabilisierte nicht- bzw. helleingefaerbte Polyamide | |
| DE1694354A1 (de) | Stabilisierte Polyphenylaether | |
| DE2509552C2 (de) | Terephthalat von 2,2'-Methylen-bis(4-methyl-6-tert.-butylphenol) sowie dessen Verwendung | |
| DE1943695B2 (de) | Mischung aus einem Epoxydharz mit 1,2-Epoxydgruppen und einem Härtungsmittel | |
| DE2321120B2 (de) | Verfahren zur Stabilisierung von Polyesteramiden | |
| DE2308225A1 (de) | Pvc-mischung | |
| DE1768076A1 (de) | Normalerweise fluessiges Phosphatesterpraeparat | |
| DE849903C (de) | Verfahren zur Herstellung von Kunstharzen | |
| DE2338711C2 (de) | Brandschutzmittel-Konzentrat zum Ausrüsten von Polypropylen | |
| DE1220601B (de) | Formmassen auf Basis von festen Propylenpolymerisaten | |
| EP0302289B1 (de) | Verfahren zur Reduzierung der Formaldehydemission bei säurehärtenden Lacken auf Basis von Alkydharz-Harnstoffharz-Kombinationen | |
| DE1226784B (de) | Verfahren zum Stabilisieren von Polyolefinen | |
| DE1694455B2 (de) | Stabilisierung von polyurethanmaterialien | |
| DE3533451A1 (de) | 2,2,6,6-tetramethylpiperidylamide substituierter carbonsaeuren und die mit ihnen stabilisierten lichtbestaendigen polymermischungen | |
| DE2114235A1 (de) | Selbstverloeschende Polyamid-Formmassen | |
| DE1235577B (de) | Verfahren zum Stabilisieren von linear gebauten thermoplastischen Polyharnstoffen | |
| DE1142439B (de) | Ungiftige, gegen thermische Oxydation bestaendige Polyaethylenformmassen | |
| DE224812C (cs) | ||
| DE1962229A1 (de) | 4-Hydroxyisophthalsaeurealkylphenylester und ihre Verwendung als UV-Licht-Stabilisatoren |