JP2005511844A - 改善された光学的性質を有するシクロオレフィン共重合体樹脂 - Google Patents
改善された光学的性質を有するシクロオレフィン共重合体樹脂 Download PDFInfo
- Publication number
- JP2005511844A JP2005511844A JP2003551201A JP2003551201A JP2005511844A JP 2005511844 A JP2005511844 A JP 2005511844A JP 2003551201 A JP2003551201 A JP 2003551201A JP 2003551201 A JP2003551201 A JP 2003551201A JP 2005511844 A JP2005511844 A JP 2005511844A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- cycloolefin
- copolymer
- cycloolefin copolymer
- glass transition
- 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
- 150000001925 cycloalkenes Chemical class 0.000 title claims abstract description 35
- 230000003287 optical effect Effects 0.000 title claims abstract description 12
- 229920006026 co-polymeric resin Polymers 0.000 title claims abstract description 7
- 229920001577 copolymer Polymers 0.000 claims abstract description 61
- 229920005989 resin Polymers 0.000 claims abstract description 46
- 239000011347 resin Substances 0.000 claims abstract description 46
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 30
- 229930195729 fatty acid Natural products 0.000 claims abstract description 30
- 239000000194 fatty acid Substances 0.000 claims abstract description 30
- -1 fatty acid esters Chemical class 0.000 claims abstract description 29
- 230000009477 glass transition Effects 0.000 claims abstract description 28
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 claims abstract description 24
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 17
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000000314 lubricant Substances 0.000 claims abstract description 7
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 5
- 239000000203 mixture Substances 0.000 claims description 46
- 229920005604 random copolymer Polymers 0.000 claims description 14
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 8
- 239000005977 Ethylene Substances 0.000 claims description 8
- 239000003963 antioxidant agent Substances 0.000 claims description 8
- 239000002530 phenolic antioxidant Substances 0.000 claims description 8
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- OCKWAZCWKSMKNC-UHFFFAOYSA-N [3-octadecanoyloxy-2,2-bis(octadecanoyloxymethyl)propyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCCCC)(COC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC OCKWAZCWKSMKNC-UHFFFAOYSA-N 0.000 claims description 4
- 230000003078 antioxidant effect Effects 0.000 claims description 4
- 238000009826 distribution Methods 0.000 claims description 4
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims description 3
- 125000006736 (C6-C20) aryl group Chemical group 0.000 claims description 3
- FSEJJKIPRNUIFL-UHFFFAOYSA-N [2,2-bis(hydroxymethyl)-3-octadecanoyloxypropyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CO)(CO)COC(=O)CCCCCCCCCCCCCCCCC FSEJJKIPRNUIFL-UHFFFAOYSA-N 0.000 claims description 3
- 229910052794 bromium Inorganic materials 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 150000002431 hydrogen Chemical class 0.000 claims description 3
- 229910052740 iodine Inorganic materials 0.000 claims description 3
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 claims description 3
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000002015 acyclic group Chemical group 0.000 claims description 2
- 239000007858 starting material Substances 0.000 claims description 2
- 239000000654 additive Substances 0.000 description 7
- 150000004665 fatty acids Chemical class 0.000 description 7
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 5
- 229910052709 silver Inorganic materials 0.000 description 5
- 239000004332 silver Substances 0.000 description 5
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- 238000004383 yellowing Methods 0.000 description 4
- 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 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000600 sorbitol Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- 235000019445 benzyl alcohol Nutrition 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 150000003623 transition metal compounds Chemical class 0.000 description 2
- ARIWANIATODDMH-AWEZNQCLSA-N 1-lauroyl-sn-glycerol Chemical compound CCCCCCCCCCCC(=O)OC[C@@H](O)CO ARIWANIATODDMH-AWEZNQCLSA-N 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- NGFBEQCLQRWZGA-UHFFFAOYSA-N C.C=CC(C(=O)O)C1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C.C=CC(C(=O)O)C1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C.C=CC(C(=O)O)C1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C.C=CC(C(=O)O)C1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C Chemical compound C.C=CC(C(=O)O)C1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C.C=CC(C(=O)O)C1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C.C=CC(C(=O)O)C1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C.C=CC(C(=O)O)C1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C NGFBEQCLQRWZGA-UHFFFAOYSA-N 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000004262 Ethyl gallate Substances 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- ARIWANIATODDMH-UHFFFAOYSA-N Lauric acid monoglyceride Natural products CCCCCCCCCCCC(=O)OCC(O)CO ARIWANIATODDMH-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 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
- 229940116226 behenic acid Drugs 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- UHUSDOQQWJGJQS-UHFFFAOYSA-N glycerol 1,2-dioctadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCCCCCCCCCCCC UHUSDOQQWJGJQS-UHFFFAOYSA-N 0.000 description 1
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 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
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000013307 optical fiber Substances 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical compound OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 229920000636 poly(norbornene) polymer Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L45/00—Compositions of homopolymers or copolymers of compounds having no unsaturated aliphatic radicals in side chain, and having one or more carbon-to-carbon double bonds in a carbocyclic or in a heterocyclic ring system; Compositions of derivatives of such polymers
-
- 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
- C08K5/101—Esters; Ether-esters of monocarboxylic acids
- C08K5/103—Esters; Ether-esters of monocarboxylic acids with polyalcohols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F232/00—Copolymers of cyclic compounds containing no unsaturated aliphatic radicals in a side chain, and having one or more carbon-to-carbon double bonds in a carbocyclic ring system
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)
- Optical Record Carriers And Manufacture Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/016,334 US6951898B2 (en) | 2001-12-10 | 2001-12-10 | Cycloolefin copolymer resins having improved optical properties |
| PCT/US2002/039295 WO2003050179A1 (en) | 2001-12-10 | 2002-12-09 | Cycloolefin copolymer resins having improved optical properties |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005511844A true JP2005511844A (ja) | 2005-04-28 |
| JP2005511844A5 JP2005511844A5 (enExample) | 2006-02-02 |
Family
ID=21776615
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003551201A Pending JP2005511844A (ja) | 2001-12-10 | 2002-12-09 | 改善された光学的性質を有するシクロオレフィン共重合体樹脂 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US6951898B2 (enExample) |
| EP (1) | EP1451247B1 (enExample) |
| JP (1) | JP2005511844A (enExample) |
| KR (1) | KR20040068934A (enExample) |
| CN (1) | CN1266205C (enExample) |
| DE (1) | DE60223837T2 (enExample) |
| TW (1) | TWI297345B (enExample) |
| WO (1) | WO2003050179A1 (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008542460A (ja) * | 2005-05-27 | 2008-11-27 | バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ | 良好な白化抵抗を有するポリオレフィン性組成物 |
| JP2012510548A (ja) * | 2008-12-01 | 2012-05-10 | エメリー・オレオケミカルス・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | 熱可塑性ポリマー用潤滑剤 |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040170785A1 (en) * | 2003-02-28 | 2004-09-02 | Wurtzel Kenneth Charles | Cosmetic containers |
| US8668971B2 (en) * | 2003-03-12 | 2014-03-11 | Fujimori Kogyo Co., Ltd. | Multiple compartment container |
| JP4183546B2 (ja) * | 2003-04-11 | 2008-11-19 | 独立行政法人理化学研究所 | テラヘルツ波光学系 |
| EP1505382A1 (en) * | 2003-08-08 | 2005-02-09 | Albert-Ludwigs-Universität Freiburg | Use of the plastic materials topas and zeonex for biotechnological applications in the terahertz range |
| KR20060084256A (ko) * | 2005-01-19 | 2006-07-24 | 삼성전자주식회사 | 액정 표시 장치용 발광 다이오드 소자의 렌즈 조성물,이를 포함하는 발광 다이오드 소자, 백라이트 유닛 및액정 표시 장치 |
| WO2009055427A2 (en) | 2007-10-22 | 2009-04-30 | Becton, Dickinson And Company | Methods for evaluating the aggregation of a protein in a suspension including organopolysiloxane and medical articles coated with organopolysiloxane containing a protein solution |
| GB0721065D0 (en) | 2007-10-26 | 2007-12-05 | Fujifilm Imaging Colorants Ltd | Improvements in and relating to toners made from latexes |
| ES2910551T3 (es) | 2008-09-22 | 2022-05-12 | Becton Dickinson Co | Un sistema para revestir el interior de un recipiente usando un método de deposición química en fase vapor asistida por fotólisis |
| US8802603B2 (en) | 2010-06-17 | 2014-08-12 | Becton, Dickinson And Company | Medical components having coated surfaces exhibiting low friction and low reactivity |
| US10342735B2 (en) | 2015-06-11 | 2019-07-09 | Tokitae Llc | Multi-monodose containers |
| US10077122B2 (en) | 2015-06-11 | 2018-09-18 | Tokitae Llc | Method of packaging multi-monodose containers |
| US20160361232A1 (en) | 2015-06-11 | 2016-12-15 | Tokitae Llc | Packaging Multi-Monodose Containers |
| US10732145B2 (en) | 2015-09-22 | 2020-08-04 | Bio-Rad Laboratories, Inc. | Electrophoresis receptacles and methods |
| ES2797298T3 (es) | 2016-02-10 | 2020-12-01 | Becton Dickinson France | Procedimiento para evaluar la estabilidad de una formulación a base de proteína |
| CN106188616A (zh) * | 2016-07-21 | 2016-12-07 | 嘉兴瑞勒新材料科技有限公司 | 烯烃扩链酸润滑剂、其制备及含该润滑剂的热塑性塑料 |
| US10988274B2 (en) * | 2017-02-07 | 2021-04-27 | Adhezion Biomedical, Llc | Packaging for adhesive compositions |
| US20250073123A1 (en) | 2023-08-30 | 2025-03-06 | Becton, Dickinson And Company | Medical Device Comprising Self-Lubricating Rubber Component |
| CN118496584B (zh) * | 2024-07-18 | 2025-02-18 | 拓烯科技(衢州)有限公司 | 一种改性环烯烃共聚物及其制备方法和应用 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE234882T1 (de) * | 1987-05-01 | 2003-04-15 | Mitsui Chemicals Inc | Ungeordnete cycloolefincopolymerzusammensetzungen und deren anwendung |
| US5270393A (en) * | 1990-10-24 | 1993-12-14 | Mitsui Petrochemical Industries, Ltd. | Ethylene cycloolefin random copolymer compositions |
| DE4233851A1 (de) * | 1992-10-08 | 1994-04-14 | Hoechst Ag | Substrat aus zumindest einem Cycloolefin-Copolymer für Aufzeichnungsmedien und Verfahren zu seiner Herstellung |
| US5965665A (en) * | 1997-08-07 | 1999-10-12 | General Electric Company | Low gloss thermoplastic resin composition |
-
2001
- 2001-12-10 US US10/016,334 patent/US6951898B2/en not_active Expired - Fee Related
-
2002
- 2002-12-09 DE DE60223837T patent/DE60223837T2/de not_active Expired - Fee Related
- 2002-12-09 KR KR10-2004-7008814A patent/KR20040068934A/ko not_active Ceased
- 2002-12-09 JP JP2003551201A patent/JP2005511844A/ja active Pending
- 2002-12-09 TW TW091135546A patent/TWI297345B/zh not_active IP Right Cessation
- 2002-12-09 CN CNB028246314A patent/CN1266205C/zh not_active Expired - Fee Related
- 2002-12-09 WO PCT/US2002/039295 patent/WO2003050179A1/en not_active Ceased
- 2002-12-09 EP EP02795787A patent/EP1451247B1/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008542460A (ja) * | 2005-05-27 | 2008-11-27 | バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ | 良好な白化抵抗を有するポリオレフィン性組成物 |
| JP2012510548A (ja) * | 2008-12-01 | 2012-05-10 | エメリー・オレオケミカルス・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | 熱可塑性ポリマー用潤滑剤 |
Also Published As
| Publication number | Publication date |
|---|---|
| US6951898B2 (en) | 2005-10-04 |
| EP1451247B1 (en) | 2007-11-28 |
| TW200303894A (en) | 2003-09-16 |
| TWI297345B (en) | 2008-06-01 |
| DE60223837D1 (de) | 2008-01-10 |
| CN1266205C (zh) | 2006-07-26 |
| DE60223837T2 (de) | 2008-10-23 |
| CN1602336A (zh) | 2005-03-30 |
| EP1451247A1 (en) | 2004-09-01 |
| KR20040068934A (ko) | 2004-08-02 |
| WO2003050179A1 (en) | 2003-06-19 |
| US20030149148A1 (en) | 2003-08-07 |
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