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 (https=) | 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 (https=) |
| EP (1) | EP1451247B1 (https=) |
| JP (1) | JP2005511844A (https=) |
| KR (1) | KR20040068934A (https=) |
| CN (1) | CN1266205C (https=) |
| DE (1) | DE60223837T2 (https=) |
| TW (1) | TWI297345B (https=) |
| WO (1) | WO2003050179A1 (https=) |
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 |
| JP4987298B2 (ja) * | 2003-03-12 | 2012-07-25 | 藤森工業株式会社 | 複室容器 |
| 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 |
| CN101889209A (zh) * | 2007-10-22 | 2010-11-17 | 贝克顿·迪金森公司 | 评价在含有机基聚硅氧烷的悬浮液中蛋白质聚集的方法和用含蛋白质溶液的有机基聚硅氧烷涂布的医疗制品 |
| GB0721065D0 (en) | 2007-10-26 | 2007-12-05 | Fujifilm Imaging Colorants Ltd | Improvements in and relating to toners made from latexes |
| EP3536363A1 (en) | 2008-09-22 | 2019-09-11 | Becton, Dickinson and Company | Systems for coating the interior of a container |
| US8802603B2 (en) | 2010-06-17 | 2014-08-12 | Becton, Dickinson And Company | Medical components having coated surfaces exhibiting low friction and low reactivity |
| 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 |
| US10342735B2 (en) | 2015-06-11 | 2019-07-09 | Tokitae Llc | Multi-monodose containers |
| EP3353538B1 (en) | 2015-09-22 | 2024-04-10 | Bio-Rad Laboratories, Inc. | Electrophoresis receptacle and method |
| CN107063940B (zh) | 2016-02-10 | 2019-10-18 | 贝克顿迪金森法国公司 | 用于评价基于蛋白质的制剂的稳定性的方法 |
| 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 |
|---|---|---|---|---|
| SG64882A1 (en) * | 1987-05-01 | 2001-06-19 | Mitsui Chemicals Inc | Cycloolefin type random copolymer compositions and uses thereof |
| 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 JP JP2003551201A patent/JP2005511844A/ja active Pending
- 2002-12-09 WO PCT/US2002/039295 patent/WO2003050179A1/en not_active Ceased
- 2002-12-09 KR KR10-2004-7008814A patent/KR20040068934A/ko not_active Ceased
- 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 EP EP02795787A patent/EP1451247B1/en not_active Expired - Lifetime
- 2002-12-09 DE DE60223837T patent/DE60223837T2/de not_active Expired - Fee Related
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 |
|---|---|
| EP1451247A1 (en) | 2004-09-01 |
| CN1602336A (zh) | 2005-03-30 |
| EP1451247B1 (en) | 2007-11-28 |
| US20030149148A1 (en) | 2003-08-07 |
| DE60223837D1 (de) | 2008-01-10 |
| WO2003050179A1 (en) | 2003-06-19 |
| TWI297345B (en) | 2008-06-01 |
| TW200303894A (en) | 2003-09-16 |
| CN1266205C (zh) | 2006-07-26 |
| US6951898B2 (en) | 2005-10-04 |
| KR20040068934A (ko) | 2004-08-02 |
| DE60223837T2 (de) | 2008-10-23 |
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