NL1009288C2 - UV stabiele polyetherester copolymeer samenstelling en folie daarvan. - Google Patents
UV stabiele polyetherester copolymeer samenstelling en folie daarvan. Download PDFInfo
- Publication number
- NL1009288C2 NL1009288C2 NL1009288A NL1009288A NL1009288C2 NL 1009288 C2 NL1009288 C2 NL 1009288C2 NL 1009288 A NL1009288 A NL 1009288A NL 1009288 A NL1009288 A NL 1009288A NL 1009288 C2 NL1009288 C2 NL 1009288C2
- Authority
- NL
- Netherlands
- Prior art keywords
- hals
- copolymer composition
- composition according
- polyether ester
- ester copolymer
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 35
- 229920001577 copolymer Polymers 0.000 title claims abstract description 18
- 239000011888 foil Substances 0.000 title claims description 15
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 39
- 150000001412 amines Chemical class 0.000 claims abstract description 8
- 239000004611 light stabiliser Substances 0.000 claims abstract description 6
- 150000002148 esters Chemical class 0.000 claims description 21
- 229910052799 carbon Inorganic materials 0.000 claims description 18
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 11
- 229920000570 polyether Polymers 0.000 claims description 11
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 7
- 239000002245 particle Substances 0.000 claims description 7
- JLZIIHMTTRXXIN-UHFFFAOYSA-N 2-(2-hydroxy-4-methoxybenzoyl)benzoic acid Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1C(O)=O JLZIIHMTTRXXIN-UHFFFAOYSA-N 0.000 claims description 6
- 239000006185 dispersion Substances 0.000 claims description 6
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 4
- 239000011164 primary particle Substances 0.000 claims description 4
- 229920000233 poly(alkylene oxides) Polymers 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 2
- 238000011835 investigation Methods 0.000 claims 2
- 239000013589 supplement Substances 0.000 claims 1
- -1 alkylene glycols Chemical class 0.000 description 25
- 238000002474 experimental method Methods 0.000 description 11
- 239000010408 film Substances 0.000 description 11
- 230000000694 effects Effects 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 7
- 230000005855 radiation Effects 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 4
- 239000007983 Tris buffer Substances 0.000 description 4
- 239000012528 membrane Substances 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 229920010784 Arnitel® EM400 Polymers 0.000 description 3
- 239000004594 Masterbatch (MB) Substances 0.000 description 3
- 239000012963 UV stabilizer Substances 0.000 description 3
- 230000032683 aging Effects 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 150000002334 glycols Chemical class 0.000 description 3
- 125000001841 imino group Chemical group [H]N=* 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- HNTWDNMNGNBFEA-UHFFFAOYSA-N 3,3,5,5-tetramethylpiperazin-2-one Chemical compound CC1(C)CNC(=O)C(C)(C)N1 HNTWDNMNGNBFEA-UHFFFAOYSA-N 0.000 description 2
- STEYNUVPFMIUOY-UHFFFAOYSA-N 4-Hydroxy-1-(2-hydroxyethyl)-2,2,6,6-tetramethylpiperidine Chemical compound CC1(C)CC(O)CC(C)(C)N1CCO STEYNUVPFMIUOY-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 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
- 239000002253 acid Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 230000002431 foraging effect Effects 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 239000001384 succinic acid Substances 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- 150000003852 triazoles Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- HOLZCMFSCBLOLX-UHFFFAOYSA-N 1-octadecylpyrrole-2,5-dione Chemical compound CCCCCCCCCCCCCCCCCCN1C(=O)C=CC1=O HOLZCMFSCBLOLX-UHFFFAOYSA-N 0.000 description 1
- DVIFVFGPATZWCB-UHFFFAOYSA-N 2-[4,4-bis(1,2,2,6,6-pentamethylpiperidin-3-yl)butyl]-2-[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]propanedioic acid Chemical compound CC1(C)N(C)C(C)(C)CCC1C(C1C(N(C)C(C)(C)CC1)(C)C)CCCC(C(O)=O)(C(O)=O)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 DVIFVFGPATZWCB-UHFFFAOYSA-N 0.000 description 1
- RLHGFJMGWQXPBW-UHFFFAOYSA-N 2-hydroxy-3-(1h-imidazol-5-ylmethyl)benzamide Chemical compound NC(=O)C1=CC=CC(CC=2NC=NC=2)=C1O RLHGFJMGWQXPBW-UHFFFAOYSA-N 0.000 description 1
- FBIXXCXCZOZFCO-UHFFFAOYSA-N 3-dodecyl-1-(2,2,6,6-tetramethylpiperidin-4-yl)pyrrolidine-2,5-dione Chemical compound O=C1C(CCCCCCCCCCCC)CC(=O)N1C1CC(C)(C)NC(C)(C)C1 FBIXXCXCZOZFCO-UHFFFAOYSA-N 0.000 description 1
- JLACFGSVTHUABX-UHFFFAOYSA-N 5-oxo-5-[1,2,3-tris(1,2,2,6,6-pentamethylpiperidin-4-yl)tridecan-4-yloxy]pentane-1,2,3-tricarboxylic acid Chemical compound C1C(C)(C)N(C)C(C)(C)CC1C(C(OC(=O)CC(C(CC(O)=O)C(O)=O)C(O)=O)CCCCCCCCC)C(C1CC(C)(C)N(C)C(C)(C)C1)CC1CC(C)(C)N(C)C(C)(C)C1 JLACFGSVTHUABX-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FMRHJJZUHUTGKE-UHFFFAOYSA-N Ethylhexyl salicylate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1O FMRHJJZUHUTGKE-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- 239000013036 UV Light Stabilizer Substances 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- CMXLJKWFEJEFJE-UHFFFAOYSA-N bis(1,2,2,6,6-pentamethylpiperidin-4-yl) 2-[(4-methoxyphenyl)methylidene]propanedioate Chemical compound C1=CC(OC)=CC=C1C=C(C(=O)OC1CC(C)(C)N(C)C(C)(C)C1)C(=O)OC1CC(C)(C)N(C)C(C)(C)C1 CMXLJKWFEJEFJE-UHFFFAOYSA-N 0.000 description 1
- GOJOVSYIGHASEI-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) butanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCC(=O)OC1CC(C)(C)NC(C)(C)C1 GOJOVSYIGHASEI-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical compound OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 description 1
- WTVNFKVGGUWHQC-UHFFFAOYSA-N decane-2,4-dione Chemical compound CCCCCCC(=O)CC(C)=O WTVNFKVGGUWHQC-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine powder Natural products NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- HYONQIJZVYCWOP-UHFFFAOYSA-N n',n'-bis(2,2,6,6-tetramethylpiperidin-4-yl)hexane-1,6-diamine Chemical compound C1C(C)(C)NC(C)(C)CC1N(CCCCCCN)C1CC(C)(C)NC(C)(C)C1 HYONQIJZVYCWOP-UHFFFAOYSA-N 0.000 description 1
- ORECYURYFJYPKY-UHFFFAOYSA-N n,n'-bis(2,2,6,6-tetramethylpiperidin-4-yl)hexane-1,6-diamine;2,4,6-trichloro-1,3,5-triazine;2,4,4-trimethylpentan-2-amine Chemical compound CC(C)(C)CC(C)(C)N.ClC1=NC(Cl)=NC(Cl)=N1.C1C(C)(C)NC(C)(C)CC1NCCCCCCNC1CC(C)(C)NC(C)(C)C1 ORECYURYFJYPKY-UHFFFAOYSA-N 0.000 description 1
- FDAKZQLBIFPGSV-UHFFFAOYSA-N n-butyl-2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CCCCNC1CC(C)(C)NC(C)(C)C1 FDAKZQLBIFPGSV-UHFFFAOYSA-N 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 125000005936 piperidyl group Chemical group 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- 229960002920 sorbitol Drugs 0.000 description 1
- 235000010356 sorbitol Nutrition 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000009864 tensile test Methods 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
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- JWUXJYZVKZKLTJ-UHFFFAOYSA-N triacetone amine Natural products CC1(C)CC(=O)CC(C)(C)N1 JWUXJYZVKZKLTJ-UHFFFAOYSA-N 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31786—Of polyester [e.g., alkyd, etc.]
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)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Polyesters Or Polycarbonates (AREA)
Priority Applications (13)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL1009288A NL1009288C2 (nl) | 1998-05-29 | 1998-05-29 | UV stabiele polyetherester copolymeer samenstelling en folie daarvan. |
| DE69910218T DE69910218T2 (de) | 1998-05-29 | 1999-05-27 | Film aus uv-stabiler polyetherester copolymer-zusammensetzung |
| PCT/NL1999/000331 WO1999062997A1 (en) | 1998-05-29 | 1999-05-27 | Uv stable polyetherester copolymer composition and film therefrom |
| AT99925467T ATE246713T1 (de) | 1998-05-29 | 1999-05-27 | Film aus uv-stabiler polyetherester copolymer- zusammensetzung |
| AU41734/99A AU4173499A (en) | 1998-05-29 | 1999-05-27 | Uv stable polyetherester copolymer composition and film therefrom |
| NZ508476A NZ508476A (en) | 1998-05-29 | 1999-05-27 | UV stable polyetherester copolymer composition and film therefrom |
| EP99925467A EP1100844B1 (en) | 1998-05-29 | 1999-05-27 | Film from uv stable polyetherester copolymer composition |
| CNB998067695A CN100360603C (zh) | 1998-05-29 | 1999-05-27 | 紫外稳定的聚醚酯共聚物组合物及由其制造的薄膜 |
| CA002333462A CA2333462C (en) | 1998-05-29 | 1999-05-27 | Uv stable polyetherester copolymer composition and film therefrom |
| HU0102214A HU227483B1 (hu) | 1998-05-29 | 1999-05-27 | Ultraibolya fénynek ellenálló poli(éter-észter)kopolimer kompozíció és az abból készült fólia |
| PL344441A PL198282B1 (pl) | 1998-05-29 | 1999-05-27 | Kompozycja kopolimeru polieteroestrowego i jej zastosowanie |
| CZ20004251A CZ300066B6 (cs) | 1998-05-29 | 1999-05-27 | Polyetheresterová kopolymerní kompozice, fólie a její použití |
| US09/722,416 US6534585B1 (en) | 1998-05-29 | 2000-11-28 | UV stable polyetherester copolymer composition and film therefrom |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL1009288 | 1998-05-29 | ||
| NL1009288A NL1009288C2 (nl) | 1998-05-29 | 1998-05-29 | UV stabiele polyetherester copolymeer samenstelling en folie daarvan. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL1009288C2 true NL1009288C2 (nl) | 1999-11-30 |
Family
ID=19767229
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL1009288A NL1009288C2 (nl) | 1998-05-29 | 1998-05-29 | UV stabiele polyetherester copolymeer samenstelling en folie daarvan. |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US6534585B1 (cs) |
| EP (1) | EP1100844B1 (cs) |
| CN (1) | CN100360603C (cs) |
| AT (1) | ATE246713T1 (cs) |
| AU (1) | AU4173499A (cs) |
| CA (1) | CA2333462C (cs) |
| CZ (1) | CZ300066B6 (cs) |
| DE (1) | DE69910218T2 (cs) |
| HU (1) | HU227483B1 (cs) |
| NL (1) | NL1009288C2 (cs) |
| NZ (1) | NZ508476A (cs) |
| PL (1) | PL198282B1 (cs) |
| WO (1) | WO1999062997A1 (cs) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6740406B2 (en) * | 2000-12-15 | 2004-05-25 | Kimberly-Clark Worldwide, Inc. | Coated activated carbon |
| JP4860837B2 (ja) * | 2001-06-18 | 2012-01-25 | 出光興産株式会社 | 遷移金属化合物、α−オレフィン製造用触媒及びα−オレフィンの製造方法 |
| WO2004108410A2 (en) * | 2003-06-02 | 2004-12-16 | Kappler, Inc. | Outdoor fabric |
| US7189777B2 (en) * | 2003-06-09 | 2007-03-13 | Eastman Chemical Company | Compositions and method for improving reheat rate of PET using activated carbon |
| DE10361230A1 (de) * | 2003-12-24 | 2005-07-28 | Ticona Gmbh | Verbundkörper, Verfahren zu dessen Herstellung und dessen Verwendung |
| US20060058435A1 (en) * | 2004-09-16 | 2006-03-16 | Szekely Peter L | Slush molded elastomeric layer |
| CN100432160C (zh) * | 2004-12-16 | 2008-11-12 | 汕头大学 | 水性反应型受阻胺涂料配方及涂层的光稳定化方法 |
| CN100432159C (zh) * | 2004-12-17 | 2008-11-12 | 汕头大学 | 反应型受阻胺涂料配方及涂层的光稳定化方法 |
| CN102112549B (zh) * | 2008-07-30 | 2013-03-27 | 纳幕尔杜邦公司 | 包含多羟基聚合物的耐热热塑性制品 |
| WO2010094559A1 (en) * | 2009-02-17 | 2010-08-26 | Dsm Ip Assets B.V. | Sheet having high water vapor permeability |
| KR101379619B1 (ko) * | 2011-01-20 | 2014-04-01 | 코오롱플라스틱 주식회사 | 열가소성 폴리에테르에스테르 엘라스토머 수지 조성물 및 이로부터 제조된 탄성 모노 필라멘트 |
| US10017639B2 (en) | 2013-12-20 | 2018-07-10 | Invista North America S.A.R.L. | Polyester-ether resin blends |
| JP6913521B2 (ja) * | 2017-06-09 | 2021-08-04 | 株式会社アズ | 機能性布帛およびその製造方法 |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4391943A (en) * | 1982-01-04 | 1983-07-05 | The Polymer Corporation | UV Stabilized nylon 6 |
| US4524165A (en) * | 1983-10-24 | 1985-06-18 | Eastman Kodak Company | Stabilized copolyesterether compositions suitable for outdoor applications |
| US4699942A (en) * | 1985-08-30 | 1987-10-13 | Eastman Kodak Co. | Polyester compositions |
| WO1996028503A1 (fr) * | 1995-03-10 | 1996-09-19 | Nyltech France | Composition a base de polyamide a stabilite lumiere elevee |
| EP0783016A2 (de) * | 1996-01-02 | 1997-07-09 | Akzo Nobel N.V. | Mit Kohlenstoffteilchen pigmentierte wasserdampfdurchlässige, wasserdichte Polyetherestermembran |
| EP0885924A2 (en) * | 1997-06-17 | 1998-12-23 | Hoechst Celanese Corporation | Improved monofilament |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3778387A (en) * | 1971-06-21 | 1973-12-11 | Calgon Corp | Activated carbon with antioxidant properties and a method of preparing the same |
| JPS61111282A (ja) * | 1984-11-02 | 1986-05-29 | Murata Mach Ltd | ワ−パ−クリ−ルへのパツケ−ジ供給装置 |
| EP0964944B1 (en) * | 1997-03-04 | 2002-08-28 | E.I. Du Pont De Nemours And Company | Uv resistant elastomeric monofilament |
-
1998
- 1998-05-29 NL NL1009288A patent/NL1009288C2/nl not_active IP Right Cessation
-
1999
- 1999-05-27 AU AU41734/99A patent/AU4173499A/en not_active Abandoned
- 1999-05-27 CZ CZ20004251A patent/CZ300066B6/cs not_active IP Right Cessation
- 1999-05-27 PL PL344441A patent/PL198282B1/pl unknown
- 1999-05-27 HU HU0102214A patent/HU227483B1/hu not_active IP Right Cessation
- 1999-05-27 DE DE69910218T patent/DE69910218T2/de not_active Expired - Lifetime
- 1999-05-27 CN CNB998067695A patent/CN100360603C/zh not_active Expired - Lifetime
- 1999-05-27 CA CA002333462A patent/CA2333462C/en not_active Expired - Lifetime
- 1999-05-27 NZ NZ508476A patent/NZ508476A/xx not_active IP Right Cessation
- 1999-05-27 AT AT99925467T patent/ATE246713T1/de active
- 1999-05-27 WO PCT/NL1999/000331 patent/WO1999062997A1/en active IP Right Grant
- 1999-05-27 EP EP99925467A patent/EP1100844B1/en not_active Expired - Lifetime
-
2000
- 2000-11-28 US US09/722,416 patent/US6534585B1/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4391943A (en) * | 1982-01-04 | 1983-07-05 | The Polymer Corporation | UV Stabilized nylon 6 |
| US4524165A (en) * | 1983-10-24 | 1985-06-18 | Eastman Kodak Company | Stabilized copolyesterether compositions suitable for outdoor applications |
| US4699942A (en) * | 1985-08-30 | 1987-10-13 | Eastman Kodak Co. | Polyester compositions |
| WO1996028503A1 (fr) * | 1995-03-10 | 1996-09-19 | Nyltech France | Composition a base de polyamide a stabilite lumiere elevee |
| EP0783016A2 (de) * | 1996-01-02 | 1997-07-09 | Akzo Nobel N.V. | Mit Kohlenstoffteilchen pigmentierte wasserdampfdurchlässige, wasserdichte Polyetherestermembran |
| EP0885924A2 (en) * | 1997-06-17 | 1998-12-23 | Hoechst Celanese Corporation | Improved monofilament |
Also Published As
| Publication number | Publication date |
|---|---|
| CZ300066B6 (cs) | 2009-01-21 |
| AU4173499A (en) | 1999-12-20 |
| CA2333462A1 (en) | 1999-12-09 |
| CN1303408A (zh) | 2001-07-11 |
| WO1999062997A1 (en) | 1999-12-09 |
| HU227483B1 (hu) | 2011-07-28 |
| ATE246713T1 (de) | 2003-08-15 |
| DE69910218T2 (de) | 2004-06-09 |
| EP1100844A1 (en) | 2001-05-23 |
| US6534585B1 (en) | 2003-03-18 |
| DE69910218D1 (de) | 2003-09-11 |
| CN100360603C (zh) | 2008-01-09 |
| HUP0102214A2 (hu) | 2001-10-28 |
| HUP0102214A3 (en) | 2002-10-28 |
| PL344441A1 (en) | 2001-11-05 |
| CZ20004251A3 (cs) | 2001-04-11 |
| CA2333462C (en) | 2009-09-01 |
| EP1100844B1 (en) | 2003-08-06 |
| NZ508476A (en) | 2003-04-29 |
| PL198282B1 (pl) | 2008-06-30 |
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| Date | Code | Title | Description |
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| PD2B | A search report has been drawn up | ||
| SD | Assignments of patents |
Owner name: DSM IP ASSETS B.V. Effective date: 20050915 |
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| TD | Modifications of names of proprietors of patents |
Owner name: KONINKLIJKE DSM N.V. Effective date: 20050915 |
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| VD1 | Lapsed due to non-payment of the annual fee |
Effective date: 20061201 |