ES2630713T3 - TPU hidrofóbico transparente - Google Patents
TPU hidrofóbico transparente Download PDFInfo
- Publication number
- ES2630713T3 ES2630713T3 ES14705001.7T ES14705001T ES2630713T3 ES 2630713 T3 ES2630713 T3 ES 2630713T3 ES 14705001 T ES14705001 T ES 14705001T ES 2630713 T3 ES2630713 T3 ES 2630713T3
- Authority
- ES
- Spain
- Prior art keywords
- chain extender
- mixture
- reaction
- diol
- carbon atoms
- 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.)
- Active
Links
- 230000002209 hydrophobic effect Effects 0.000 title claims abstract description 41
- 239000004970 Chain extender Substances 0.000 claims abstract description 95
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims abstract description 93
- 239000004433 Thermoplastic polyurethane Substances 0.000 claims abstract description 68
- 239000000203 mixture Substances 0.000 claims abstract description 52
- 229920005862 polyol Polymers 0.000 claims abstract description 41
- 150000003077 polyols Chemical class 0.000 claims abstract description 40
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 28
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 25
- 239000000194 fatty acid Substances 0.000 claims abstract description 25
- 229930195729 fatty acid Natural products 0.000 claims abstract description 25
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 24
- 125000005442 diisocyanate group Chemical group 0.000 claims abstract description 20
- 150000002009 diols Chemical group 0.000 claims abstract description 18
- 229920000642 polymer Polymers 0.000 claims abstract description 18
- 239000003054 catalyst Substances 0.000 claims abstract description 15
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229920005906 polyester polyol Polymers 0.000 claims abstract description 8
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 3
- 238000006243 chemical reaction Methods 0.000 claims description 45
- 238000000034 method Methods 0.000 claims description 32
- DSKYSDCYIODJPC-UHFFFAOYSA-N 2-butyl-2-ethylpropane-1,3-diol Chemical group CCCCC(CC)(CO)CO DSKYSDCYIODJPC-UHFFFAOYSA-N 0.000 claims description 23
- 239000011541 reaction mixture Substances 0.000 claims description 12
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical group C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 claims description 10
- GHLKSLMMWAKNBM-UHFFFAOYSA-N dodecane-1,12-diol Chemical group OCCCCCCCCCCCCO GHLKSLMMWAKNBM-UHFFFAOYSA-N 0.000 claims description 10
- 239000007788 liquid Substances 0.000 claims description 10
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 4
- 239000008240 homogeneous mixture Substances 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims 1
- 239000003153 chemical reaction reagent Substances 0.000 description 17
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 12
- 239000008188 pellet Substances 0.000 description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 9
- 239000012948 isocyanate Substances 0.000 description 7
- 150000002513 isocyanates Chemical class 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 230000005484 gravity Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 238000010923 batch production Methods 0.000 description 3
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 3
- 239000000539 dimer Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000005059 1,4-Cyclohexyldiisocyanate Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- -1 aliphatic monocarboxylic acids Chemical class 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 239000002981 blocking agent Substances 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical compound CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RTTZISZSHSCFRH-UHFFFAOYSA-N 1,3-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC(CN=C=O)=C1 RTTZISZSHSCFRH-UHFFFAOYSA-N 0.000 description 1
- ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 description 1
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
- JRQLZCFSWYQHPI-UHFFFAOYSA-N 4,5-dichloro-2-cyclohexyl-1,2-thiazol-3-one Chemical compound O=C1C(Cl)=C(Cl)SN1C1CCCCC1 JRQLZCFSWYQHPI-UHFFFAOYSA-N 0.000 description 1
- SIJNQSUSNJLGSC-UHFFFAOYSA-N C(CCCCCCCCCCC)(=O)O.C(CCCCCCCCCCC)(=O)O.C(CCC)CCCCC Chemical compound C(CCCCCCCCCCC)(=O)O.C(CCCCCCCCCCC)(=O)O.C(CCC)CCCCC SIJNQSUSNJLGSC-UHFFFAOYSA-N 0.000 description 1
- 101100188975 Caenorhabditis elegans ddo-3 gene Proteins 0.000 description 1
- 206010072064 Exposure to body fluid Diseases 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920005830 Polyurethane Foam Polymers 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- 230000000447 dimerizing effect Effects 0.000 description 1
- GTZOYNFRVVHLDZ-UHFFFAOYSA-N dodecane-1,1-diol Chemical compound CCCCCCCCCCCC(O)O GTZOYNFRVVHLDZ-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- LZKLAOYSENRNKR-LNTINUHCSA-N iron;(z)-4-oxoniumylidenepent-2-en-2-olate Chemical compound [Fe].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O LZKLAOYSENRNKR-LNTINUHCSA-N 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- VQPKAMAVKYTPLB-UHFFFAOYSA-N lead;octanoic acid Chemical compound [Pb].CCCCCCCC(O)=O VQPKAMAVKYTPLB-UHFFFAOYSA-N 0.000 description 1
- AKTIAGQCYPCKFX-FDGPNNRMSA-L magnesium;(z)-4-oxopent-2-en-2-olate Chemical compound [Mg+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O AKTIAGQCYPCKFX-FDGPNNRMSA-L 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- OOCYPIXCHKROMD-UHFFFAOYSA-M phenyl(propanoyloxy)mercury Chemical compound CCC(=O)O[Hg]C1=CC=CC=C1 OOCYPIXCHKROMD-UHFFFAOYSA-M 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000011496 polyurethane foam Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
Classifications
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6603—Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
- C08G18/6607—Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6633—Compounds of group C08G18/42
- C08G18/6637—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38
- C08G18/664—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B9/00—Making granules
- B29B9/02—Making granules by dividing preformed material
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4236—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups
- C08G18/4238—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups derived from dicarboxylic acids and dialcohols
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
- C08G18/7657—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
- C08G18/7664—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
- C08G18/7671—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups containing only one alkylene bisphenyl group
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Polyurethanes Or Polyureas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361760352P | 2013-02-04 | 2013-02-04 | |
| US201361760352P | 2013-02-04 | ||
| PCT/US2014/014373 WO2014121174A1 (en) | 2013-02-04 | 2014-02-03 | Clear hydrophobic tpu |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2630713T3 true ES2630713T3 (es) | 2017-08-23 |
Family
ID=50114589
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES14705001.7T Active ES2630713T3 (es) | 2013-02-04 | 2014-02-03 | TPU hidrofóbico transparente |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US20150368392A1 (https=) |
| EP (1) | EP2951224B1 (https=) |
| JP (1) | JP6363105B2 (https=) |
| KR (1) | KR102171723B1 (https=) |
| CN (1) | CN104955860B (https=) |
| AU (1) | AU2014212059B2 (https=) |
| BR (1) | BR112015018472B1 (https=) |
| CA (1) | CA2899226C (https=) |
| CR (1) | CR20150398A (https=) |
| ES (1) | ES2630713T3 (https=) |
| MX (1) | MX380882B (https=) |
| MY (1) | MY169924A (https=) |
| SG (1) | SG11201505805SA (https=) |
| TW (1) | TWI624486B (https=) |
| WO (1) | WO2014121174A1 (https=) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI568792B (zh) * | 2015-12-17 | 2017-02-01 | 財團法人工業技術研究院 | 用於電容去離子電極的黏結劑與其形成方法 |
| CN111269381B (zh) * | 2018-12-05 | 2022-04-22 | 万华化学集团股份有限公司 | 一种用于颜色浓缩物载体的热塑性聚氨酯 |
| JP7171922B2 (ja) | 2018-12-21 | 2022-11-15 | ダウ グローバル テクノロジーズ エルエルシー | ２成分無溶剤接着剤組成物 |
| JP2022531375A (ja) * | 2019-05-03 | 2022-07-06 | スリーエム イノベイティブ プロパティズ カンパニー | 熱可塑性ポリウレタンフィルム及びそれから形成される歯科装具 |
| KR102509426B1 (ko) * | 2019-12-13 | 2023-03-13 | 주식회사 아이센스 | 비혼합형 양친매성 열가소성 폴리우레탄, 이의 제조방법 및 이를 포함하는 삽입형 의료장치 |
| TW202248261A (zh) | 2021-04-19 | 2022-12-16 | 美商貝伊材料有限責任公司 | 具有改良的應力保持性及耐濕性的聚氨酯組成物 |
| CN113980217A (zh) * | 2021-10-22 | 2022-01-28 | 东莞市米儿塑胶原料有限公司 | 一种透明tpu的制备方法 |
| CN114751828B (zh) * | 2022-04-20 | 2023-08-29 | 江苏恒力化纤股份有限公司 | 羟基封端油酸酯、环保型疏水聚氨酯及其制备方法和应用 |
| CN115197391B (zh) * | 2022-08-15 | 2023-10-31 | 河北邦泰氨纶科技有限公司 | 一种纤维级聚氨酯切片及其制备方法和应用 |
| CN116217882A (zh) * | 2022-12-07 | 2023-06-06 | 山东一诺威聚氨酯股份有限公司 | 隐形车衣高强度低雾度tpu及其制备方法 |
| WO2025191134A1 (en) | 2024-03-14 | 2025-09-18 | Analog Devices International Unlimited Company | Chloride sensor |
| WO2026013182A2 (en) | 2024-07-10 | 2026-01-15 | Analog Devices International Unlimited Company | Membrane for reference electrode |
| CN119143963B (zh) * | 2024-11-18 | 2025-01-24 | 山东一诺威聚氨酯股份有限公司 | 一种兼具导热和自清洁的tpu材料及其制备方法与应用 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3930523A1 (de) * | 1989-09-13 | 1991-03-21 | Bayer Ag | Polyurethanelastomere mit geringer haerte |
| JPH06211959A (ja) * | 1993-01-18 | 1994-08-02 | Toagosei Chem Ind Co Ltd | ポリウレタン用組成物 |
| US8357768B2 (en) * | 2005-12-09 | 2013-01-22 | Hani Farah | Low haze thermoplastic polyurethane using co-chain extenders |
| WO2008121133A1 (en) * | 2007-03-29 | 2008-10-09 | Lubrizol Advanced Materials, Inc. | Low haze thermoplastic polyurethane using mixture of chain extenders including 1,3-and 1,4-cyclohexanedimethanol |
| AU2009206538B2 (en) * | 2008-01-24 | 2014-07-10 | Lubrizol Advanced Materials, Inc. | Soft thermoplastic elastomer composition |
| US8802770B2 (en) | 2008-01-24 | 2014-08-12 | Lubrizol Advanced Materials, Inc. | Hydrophobic thermoplastic polyurethane |
| US20110135899A1 (en) * | 2008-08-06 | 2011-06-09 | Lubrizol Advanced Materials, Inc. | Films And Articles Made With Thermoplastic Block Copolymers |
| US8273845B2 (en) | 2008-09-02 | 2012-09-25 | Lubrizol Advanced Materials, Inc. | Soft thermoplastic elastomer composition |
| JP5350315B2 (ja) * | 2010-05-11 | 2013-11-27 | 三井化学株式会社 | ポリウレタンエラストマーおよび成形品 |
-
2014
- 2014-02-03 KR KR1020157023721A patent/KR102171723B1/ko not_active Expired - Fee Related
- 2014-02-03 SG SG11201505805SA patent/SG11201505805SA/en unknown
- 2014-02-03 ES ES14705001.7T patent/ES2630713T3/es active Active
- 2014-02-03 EP EP14705001.7A patent/EP2951224B1/en active Active
- 2014-02-03 BR BR112015018472-3A patent/BR112015018472B1/pt active IP Right Grant
- 2014-02-03 WO PCT/US2014/014373 patent/WO2014121174A1/en not_active Ceased
- 2014-02-03 CA CA2899226A patent/CA2899226C/en active Active
- 2014-02-03 AU AU2014212059A patent/AU2014212059B2/en not_active Ceased
- 2014-02-03 JP JP2015556196A patent/JP6363105B2/ja active Active
- 2014-02-03 US US14/765,657 patent/US20150368392A1/en not_active Abandoned
- 2014-02-03 MY MYPI2015702400A patent/MY169924A/en unknown
- 2014-02-03 CN CN201480006465.6A patent/CN104955860B/zh active Active
- 2014-02-03 MX MX2015009830A patent/MX380882B/es unknown
- 2014-02-05 TW TW103103741A patent/TWI624486B/zh not_active IP Right Cessation
-
2015
- 2015-07-31 CR CR20150398A patent/CR20150398A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BR112015018472B1 (pt) | 2020-12-22 |
| AU2014212059B2 (en) | 2017-02-16 |
| JP2016505090A (ja) | 2016-02-18 |
| SG11201505805SA (en) | 2015-08-28 |
| MX380882B (es) | 2025-03-12 |
| TW201434871A (zh) | 2014-09-16 |
| MY169924A (en) | 2019-06-17 |
| CA2899226A1 (en) | 2014-08-07 |
| CN104955860A (zh) | 2015-09-30 |
| CR20150398A (es) | 2015-10-07 |
| TWI624486B (zh) | 2018-05-21 |
| EP2951224A1 (en) | 2015-12-09 |
| AU2014212059A1 (en) | 2015-08-13 |
| WO2014121174A1 (en) | 2014-08-07 |
| KR102171723B1 (ko) | 2020-10-29 |
| EP2951224B1 (en) | 2017-04-05 |
| US20150368392A1 (en) | 2015-12-24 |
| MX2015009830A (es) | 2015-10-05 |
| JP6363105B2 (ja) | 2018-07-25 |
| KR20150115866A (ko) | 2015-10-14 |
| BR112015018472A2 (pt) | 2017-07-18 |
| CN104955860B (zh) | 2018-09-21 |
| CA2899226C (en) | 2020-08-25 |
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