TW200427752A - Salt-like reaction products of HALS derivatives and phosphor-containing organic acids for the stabilisation of polymeric materials - Google Patents
Salt-like reaction products of HALS derivatives and phosphor-containing organic acids for the stabilisation of polymeric materials Download PDFInfo
- Publication number
- TW200427752A TW200427752A TW093104031A TW93104031A TW200427752A TW 200427752 A TW200427752 A TW 200427752A TW 093104031 A TW093104031 A TW 093104031A TW 93104031 A TW93104031 A TW 93104031A TW 200427752 A TW200427752 A TW 200427752A
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- Prior art keywords
- acid
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- scope
- reaction product
- patent application
- Prior art date
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- 239000007795 chemical reaction product Substances 0.000 title claims abstract description 19
- 230000006641 stabilisation Effects 0.000 title abstract description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 title description 2
- 239000000463 material Substances 0.000 title description 2
- 150000007524 organic acids Chemical class 0.000 title description 2
- 235000005985 organic acids Nutrition 0.000 title 1
- 239000002253 acid Substances 0.000 claims abstract description 36
- 150000001875 compounds Chemical class 0.000 claims abstract description 34
- 239000000203 mixture Substances 0.000 claims abstract description 25
- 239000004952 Polyamide Substances 0.000 claims abstract description 14
- 229920002647 polyamide Polymers 0.000 claims abstract description 14
- 229920000642 polymer Polymers 0.000 claims abstract description 14
- 238000000034 method Methods 0.000 claims abstract description 10
- 150000007513 acids Chemical class 0.000 claims abstract description 8
- 229920000728 polyester Polymers 0.000 claims abstract description 8
- -1 Cycloaliphatic Chemical group 0.000 claims description 36
- 239000000047 product Substances 0.000 claims description 22
- 238000005469 granulation Methods 0.000 claims description 18
- 230000003179 granulation Effects 0.000 claims description 18
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 claims description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- 125000003118 aryl group Chemical group 0.000 claims description 16
- 125000001072 heteroaryl group Chemical group 0.000 claims description 13
- 125000001931 aliphatic group Chemical group 0.000 claims description 10
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- 238000003825 pressing Methods 0.000 claims description 6
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 238000001125 extrusion Methods 0.000 claims description 4
- CDXVUROVRIFQMV-UHFFFAOYSA-N oxo(diphenoxy)phosphanium Chemical compound C=1C=CC=CC=1O[P+](=O)OC1=CC=CC=C1 CDXVUROVRIFQMV-UHFFFAOYSA-N 0.000 claims description 4
- 238000005516 engineering process Methods 0.000 claims description 3
- 150000002466 imines Chemical class 0.000 claims description 3
- 239000004615 ingredient Substances 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 2
- QLZHNIAADXEJJP-UHFFFAOYSA-N Phenylphosphonic acid Chemical compound OP(O)(=O)C1=CC=CC=C1 QLZHNIAADXEJJP-UHFFFAOYSA-N 0.000 claims description 2
- MJUJXFBTEFXVKU-UHFFFAOYSA-N diethyl phosphonate Chemical compound CCOP(=O)OCC MJUJXFBTEFXVKU-UHFFFAOYSA-N 0.000 claims description 2
- ZJXZSIYSNXKHEA-UHFFFAOYSA-N ethyl dihydrogen phosphate Chemical compound CCOP(O)(O)=O ZJXZSIYSNXKHEA-UHFFFAOYSA-N 0.000 claims description 2
- GATNOFPXSDHULC-UHFFFAOYSA-N ethylphosphonic acid Chemical compound CCP(O)(O)=O GATNOFPXSDHULC-UHFFFAOYSA-N 0.000 claims description 2
- 238000002844 melting Methods 0.000 claims description 2
- 230000008018 melting Effects 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 230000005588 protonation Effects 0.000 claims description 2
- 238000005507 spraying Methods 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 230000000087 stabilizing effect Effects 0.000 claims 2
- 230000015556 catabolic process Effects 0.000 claims 1
- 238000006731 degradation reaction Methods 0.000 claims 1
- 125000001841 imino group Chemical group [H]N=* 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 150000003839 salts Chemical class 0.000 abstract description 5
- 238000002360 preparation method Methods 0.000 abstract description 4
- 229920006112 polar polymer Polymers 0.000 abstract description 2
- 229910019142 PO4 Inorganic materials 0.000 description 10
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 10
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 10
- 239000010452 phosphate Substances 0.000 description 10
- 229920000768 polyamine Polymers 0.000 description 8
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 7
- 239000000654 additive Substances 0.000 description 5
- 125000002947 alkylene group Chemical group 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 229920001707 polybutylene terephthalate Polymers 0.000 description 3
- 238000006068 polycondensation reaction Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000011105 stabilization Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- MQYFWRJEFAZXHE-UHFFFAOYSA-N (2-phenylphenyl)phosphonic acid Chemical compound OP(O)(=O)C1=CC=CC=C1C1=CC=CC=C1 MQYFWRJEFAZXHE-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 230000001588 bifunctional effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 239000004611 light stabiliser Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000012779 reinforcing material Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- AFINAILKDBCXMX-PBHICJAKSA-N (2s,3r)-2-amino-3-hydroxy-n-(4-octylphenyl)butanamide Chemical compound CCCCCCCCC1=CC=C(NC(=O)[C@@H](N)[C@@H](C)O)C=C1 AFINAILKDBCXMX-PBHICJAKSA-N 0.000 description 1
- CYXGBTZYTXLVDN-UHFFFAOYSA-N 1-octoxyphosphonoyloxyoctane Chemical compound CCCCCCCCOP(=O)OCCCCCCCC CYXGBTZYTXLVDN-UHFFFAOYSA-N 0.000 description 1
- PVBGKAMVCZUNFQ-UHFFFAOYSA-N 1-propoxyphosphonoyloxypropane Chemical compound CCCOP(=O)OCCC PVBGKAMVCZUNFQ-UHFFFAOYSA-N 0.000 description 1
- ADTQPWGJZBNMDS-UHFFFAOYSA-N 2-[oxido(2-phenylethoxy)phosphaniumyl]oxyethylbenzene Chemical compound P(OCCC1=CC=CC=C1)(OCCC1=CC=CC=C1)=O ADTQPWGJZBNMDS-UHFFFAOYSA-N 0.000 description 1
- BFDYSJCMAFSRDH-UHFFFAOYSA-N 2-phenylethylphosphonic acid Chemical compound OP(O)(=O)CCC1=CC=CC=C1 BFDYSJCMAFSRDH-UHFFFAOYSA-N 0.000 description 1
- XYJLPCAKKYOLGU-UHFFFAOYSA-N 2-phosphonoethylphosphonic acid Chemical compound OP(O)(=O)CCP(O)(O)=O XYJLPCAKKYOLGU-UHFFFAOYSA-N 0.000 description 1
- 239000004484 Briquette Substances 0.000 description 1
- DNWYBWXNHLBFFI-UHFFFAOYSA-N C1(=C(C(=CC=C1)C)C)OP(OC1=C(C(=CC=C1)C)C)=O Chemical compound C1(=C(C(=CC=C1)C)C)OP(OC1=C(C(=CC=C1)C)C)=O DNWYBWXNHLBFFI-UHFFFAOYSA-N 0.000 description 1
- GLEITGUARGOFBC-UHFFFAOYSA-N CC1=CC=CC=C1OP(=O)OC1=CC=CC=C1C Chemical compound CC1=CC=CC=C1OP(=O)OC1=CC=CC=C1C GLEITGUARGOFBC-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- HZCDANOFLILNSA-UHFFFAOYSA-N Dimethyl hydrogen phosphite Chemical compound COP(=O)OC HZCDANOFLILNSA-UHFFFAOYSA-N 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- JNJZLAHUXHBYIS-UHFFFAOYSA-N OP(O)(=O)OP1(=O)OCCO1 Chemical compound OP(O)(=O)OP1(=O)OCCO1 JNJZLAHUXHBYIS-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- IZQZNLBFNMTRMF-UHFFFAOYSA-N acetic acid;phosphoric acid Chemical compound CC(O)=O.OP(O)(O)=O IZQZNLBFNMTRMF-UHFFFAOYSA-N 0.000 description 1
- 238000003916 acid precipitation Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229920003232 aliphatic polyester Polymers 0.000 description 1
- 125000001118 alkylidene group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- UOKRBSXOBUKDGE-UHFFFAOYSA-N butylphosphonic acid Chemical compound CCCCP(O)(O)=O UOKRBSXOBUKDGE-UHFFFAOYSA-N 0.000 description 1
- QXJJQWWVWRCVQT-UHFFFAOYSA-K calcium;sodium;phosphate Chemical compound [Na+].[Ca+2].[O-]P([O-])([O-])=O QXJJQWWVWRCVQT-UHFFFAOYSA-K 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- LQQCGEGRINLHDP-UHFFFAOYSA-N carboxyphosphoric acid Chemical compound OC(=O)OP(O)(O)=O LQQCGEGRINLHDP-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000002993 cycloalkylene group Chemical group 0.000 description 1
- BKIHABIKDJAKKT-UHFFFAOYSA-N cyclohexyloxyphosphonoyloxycyclohexane Chemical compound C1CCCCC1OP(=O)OC1CCCCC1 BKIHABIKDJAKKT-UHFFFAOYSA-N 0.000 description 1
- FBSFTJQYCLLGKH-UHFFFAOYSA-N cyclohexylphosphonic acid Chemical compound OP(O)(=O)C1CCCCC1 FBSFTJQYCLLGKH-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- SMNZHEHSKZSQLM-UHFFFAOYSA-N ethyl(methoxy)phosphinic acid Chemical compound CCP(O)(=O)OC SMNZHEHSKZSQLM-UHFFFAOYSA-N 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- GJWAEWLHSDGBGG-UHFFFAOYSA-N hexylphosphonic acid Chemical compound CCCCCCP(O)(O)=O GJWAEWLHSDGBGG-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- MBKDYNNUVRNNRF-UHFFFAOYSA-N medronic acid Chemical compound OP(O)(=O)CP(O)(O)=O MBKDYNNUVRNNRF-UHFFFAOYSA-N 0.000 description 1
- 238000010128 melt processing Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- CAAULPUQFIIOTL-UHFFFAOYSA-L methyl phosphate(2-) Chemical compound COP([O-])([O-])=O CAAULPUQFIIOTL-UHFFFAOYSA-L 0.000 description 1
- YACKEPLHDIMKIO-UHFFFAOYSA-N methylphosphonic acid Chemical compound CP(O)(O)=O YACKEPLHDIMKIO-UHFFFAOYSA-N 0.000 description 1
- 239000012802 nanoclay Substances 0.000 description 1
- 239000002071 nanotube Substances 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- NJGCRMAPOWGWMW-UHFFFAOYSA-N octylphosphonic acid Chemical compound CCCCCCCCP(O)(O)=O NJGCRMAPOWGWMW-UHFFFAOYSA-N 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- FKKCPZSMQFVXFV-UHFFFAOYSA-N phosphonooxymethyl dihydrogen phosphate Chemical compound OP(O)(=O)OCOP(O)(O)=O FKKCPZSMQFVXFV-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- NNOBHPBYUHDMQF-UHFFFAOYSA-N propylphosphine Chemical compound CCCP NNOBHPBYUHDMQF-UHFFFAOYSA-N 0.000 description 1
- NQDAJUCXNKEDNN-UHFFFAOYSA-N pyridine-2,5-dione Chemical compound O=C1C=CC(=O)N=C1 NQDAJUCXNKEDNN-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3432—Six-membered rings
- C08K5/3435—Piperidines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/91—Polymers modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/48—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
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/35—Heterocyclic compounds having nitrogen in the ring having also oxygen in the ring
- C08K5/353—Five-membered rings
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)
- Polyamides (AREA)
- Hydrogenated Pyridines (AREA)
- Luminescent Compositions (AREA)
- Pyridine Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP03003939A EP1449872A1 (de) | 2003-02-21 | 2003-02-21 | Stabilisierung polymerer Materialien |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW200427752A true TW200427752A (en) | 2004-12-16 |
Family
ID=32731562
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW093104032A TW200420643A (en) | 2003-02-21 | 2004-02-19 | Salt-like reaction products of HALS derivatives and carboxylic acids for the stabilisation of polymeric materials |
| TW093104031A TW200427752A (en) | 2003-02-21 | 2004-02-19 | Salt-like reaction products of HALS derivatives and phosphor-containing organic acids for the stabilisation of polymeric materials |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW093104032A TW200420643A (en) | 2003-02-21 | 2004-02-19 | Salt-like reaction products of HALS derivatives and carboxylic acids for the stabilisation of polymeric materials |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US20060079610A1 (enExample) |
| EP (3) | EP1449872A1 (enExample) |
| JP (2) | JP2006518407A (enExample) |
| KR (2) | KR20050109487A (enExample) |
| CN (2) | CN1751088A (enExample) |
| AT (1) | ATE370190T1 (enExample) |
| DE (1) | DE602004008228T2 (enExample) |
| ES (1) | ES2291855T3 (enExample) |
| TW (2) | TW200420643A (enExample) |
| WO (2) | WO2004074365A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI513762B (zh) * | 2014-04-09 | 2015-12-21 | Fdc Lees Chemical Industry Co | 雙官能型安定劑及其組成物 |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1449872A1 (de) * | 2003-02-21 | 2004-08-25 | Clariant International Ltd. | Stabilisierung polymerer Materialien |
| JP4788865B2 (ja) * | 2004-10-04 | 2011-10-05 | 東洋紡績株式会社 | マスターバッチ用熱可塑性樹脂組成物およびその成形材料の製造方法およびそれらを用いた熱可塑性樹脂組成物およびその製造方法 |
| EP1773932B1 (en) * | 2004-06-22 | 2010-04-14 | INVISTA Technologies S.à.r.l. | Solubilized additive composition comprising acidic and basic constituents |
| US8557950B2 (en) | 2005-06-16 | 2013-10-15 | Grupo Petrotemex, S.A. De C.V. | High intrinsic viscosity melt phase polyester polymers with acceptable acetaldehyde generation rates |
| US9267007B2 (en) | 2005-09-16 | 2016-02-23 | Grupo Petrotemex, S.A. De C.V. | Method for addition of additives into a polymer melt |
| US7838596B2 (en) | 2005-09-16 | 2010-11-23 | Eastman Chemical Company | Late addition to effect compositional modifications in condensation polymers |
| DE102008026075B4 (de) * | 2008-05-30 | 2015-04-30 | Lurgi Zimmer Gmbh | Verfahren zur Herstellung von Polyamiden unter Verwendung von Carbonsäuren und Amiden |
| JP6107559B2 (ja) * | 2012-11-09 | 2017-04-05 | 豊田合成株式会社 | 発光装置 |
| KR102402244B1 (ko) * | 2014-05-21 | 2022-05-26 | 솔베이 스페셜티 폴리머즈 유에스에이, 엘.엘.씨. | 안정화제 화합물 |
| TWI671121B (zh) * | 2014-07-29 | 2019-09-11 | 荷蘭商帝斯曼知識產權資產管理有限公司 | 用於製備聚醯胺的方法、用於該方法中的耐綸鹽及用於製造該鹽的方法 |
| US10889704B2 (en) | 2017-05-22 | 2021-01-12 | Exxonmobil Chemical Patents Inc. | Halogenated elastomers with Mooney viscosity stability and method for preparing same |
| WO2018217294A1 (en) * | 2017-05-22 | 2018-11-29 | Exxonmobil Chemical Patents Inc. | Halogenated elastomers with mooney viscosity stability and method for preparing same |
| CN110650979B (zh) * | 2017-05-22 | 2022-06-14 | 埃克森美孚化学专利公司 | 具有门尼粘度稳定性的卤化弹性体及其制备方法 |
| CN112521659A (zh) * | 2020-12-07 | 2021-03-19 | 上海大学 | 一种改性紫外光稳定剂、制备方法及其应用 |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5976417A (en) * | 1909-01-07 | 1999-11-02 | Clariant Finance (Bvi) Limited | Mixtures of HALS compounds |
| JPS5263183A (en) * | 1975-11-19 | 1977-05-25 | Adeka Argus Chem Co Ltd | Stabilizer for organic materials |
| DE2862332D1 (en) * | 1977-12-30 | 1983-11-10 | Ciba Geigy Ag | Stabilisation of heat-curable metallic enamel paints against the action of light, humidity and oxygen by the addition of polyalkylpiperidine derivatives |
| EP0017617A3 (de) * | 1979-03-27 | 1980-10-29 | Ciba-Geigy Ag | Polyalkylpiperidin-spirooxazolone, ihre Verwendung als Lichtschutzmittel und mit diesen Verbindungen stabilisierter Kunststoff |
| JPS5962651A (ja) * | 1982-10-02 | 1984-04-10 | Adeka Argus Chem Co Ltd | 高分子材料用光安定剤 |
| US4619956A (en) * | 1985-05-03 | 1986-10-28 | American Cyanamid Co. | Stabilization of high solids coatings with synergistic combinations |
| US5795499A (en) * | 1989-12-26 | 1998-08-18 | Cytec Technology Corp. | Stabilization of high solids coatings with liquid compositions of triazine UV absorbers |
| IT1251687B (it) * | 1991-10-11 | 1995-05-19 | Mini Ricerca Scient Tecnolog | Sali di composti triazinici con acidi ossigenati del fosforo, e loro impiego in composizioni polimeriche autoestinguenti. |
| EP0559613B1 (de) * | 1992-03-05 | 1999-12-15 | Ciba SC Holding AG | Stabilisierung von organischen Pigmenten |
| US5616636A (en) * | 1992-03-11 | 1997-04-01 | Sandoz Ltd. | Phosphonite-hals and phosphite-hals compounds as stabilizers |
| FR2694761B1 (fr) * | 1992-08-17 | 1996-06-14 | Sandoz Sa | Amines steriquement encombrees, leur preparation et leur utilisation comme stabilisants des matieres polymeres. |
| TW237471B (enExample) * | 1992-09-03 | 1995-01-01 | Ciba Geigy | |
| GB9609742D0 (en) * | 1996-05-10 | 1996-07-17 | Clariant Int Ltd | Improvements in or relating to organic compounds |
| GB9615943D0 (en) * | 1996-07-30 | 1996-09-11 | Sandoz Ltd | Improvements in or relating to organic processes |
| US5969014A (en) * | 1997-09-23 | 1999-10-19 | Clariant Finance (Bvi) Limited | Synergistic polyamide stabilization method |
| DE19745099B4 (de) * | 1997-10-11 | 2014-11-06 | Lurgi Zimmer Gmbh | Verwendung eines Additivs mit kettenregelnden und stabilisierenden Eigenschaften bei der Herstellung von Polycaprolactam |
| US5965261A (en) * | 1998-11-16 | 1999-10-12 | Clariant Finance (Bvi) Limited | Polyester |
| FR2818985B1 (fr) * | 2000-12-29 | 2004-02-20 | Nylstar Sa | Procede de fabrication de compositions stabilisees a base de polyamide |
| EP1449872A1 (de) * | 2003-02-21 | 2004-08-25 | Clariant International Ltd. | Stabilisierung polymerer Materialien |
-
2003
- 2003-02-21 EP EP03003939A patent/EP1449872A1/de not_active Withdrawn
-
2004
- 2004-02-19 DE DE602004008228T patent/DE602004008228T2/de not_active Expired - Fee Related
- 2004-02-19 AT AT04712633T patent/ATE370190T1/de not_active IP Right Cessation
- 2004-02-19 EP EP04712630A patent/EP1597309A1/en not_active Withdrawn
- 2004-02-19 TW TW093104032A patent/TW200420643A/zh unknown
- 2004-02-19 WO PCT/IB2004/000508 patent/WO2004074365A1/en not_active Ceased
- 2004-02-19 KR KR1020057014897A patent/KR20050109487A/ko not_active Withdrawn
- 2004-02-19 JP JP2006502477A patent/JP2006518407A/ja not_active Withdrawn
- 2004-02-19 CN CNA2004800046033A patent/CN1751088A/zh active Pending
- 2004-02-19 EP EP04712633A patent/EP1597311B1/en not_active Expired - Lifetime
- 2004-02-19 ES ES04712633T patent/ES2291855T3/es not_active Expired - Lifetime
- 2004-02-19 WO PCT/IB2004/000509 patent/WO2004074364A1/en not_active Ceased
- 2004-02-19 US US10/546,503 patent/US20060079610A1/en not_active Abandoned
- 2004-02-19 CN CNA2004800046654A patent/CN1751087A/zh active Pending
- 2004-02-19 US US10/546,501 patent/US20060217467A1/en not_active Abandoned
- 2004-02-19 TW TW093104031A patent/TW200427752A/zh unknown
- 2004-02-19 JP JP2006502478A patent/JP2006518371A/ja not_active Withdrawn
- 2004-02-19 KR KR1020057014908A patent/KR20050101550A/ko not_active Withdrawn
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI513762B (zh) * | 2014-04-09 | 2015-12-21 | Fdc Lees Chemical Industry Co | 雙官能型安定劑及其組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1449872A1 (de) | 2004-08-25 |
| WO2004074365A1 (en) | 2004-09-02 |
| CN1751087A (zh) | 2006-03-22 |
| CN1751088A (zh) | 2006-03-22 |
| DE602004008228D1 (de) | 2007-09-27 |
| TW200420643A (en) | 2004-10-16 |
| EP1597309A1 (en) | 2005-11-23 |
| KR20050101550A (ko) | 2005-10-24 |
| ATE370190T1 (de) | 2007-09-15 |
| EP1597311B1 (en) | 2007-08-15 |
| ES2291855T3 (es) | 2008-03-01 |
| US20060079610A1 (en) | 2006-04-13 |
| KR20050109487A (ko) | 2005-11-21 |
| EP1597311A1 (en) | 2005-11-23 |
| US20060217467A1 (en) | 2006-09-28 |
| JP2006518371A (ja) | 2006-08-10 |
| JP2006518407A (ja) | 2006-08-10 |
| WO2004074364A1 (en) | 2004-09-02 |
| DE602004008228T2 (de) | 2008-05-15 |
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