ES2758535T3 - Copoliésteres termoplásticos de poli(furanoato de isoidida) y un uso de los mismos en el envasado de llenado en caliente - Google Patents
Copoliésteres termoplásticos de poli(furanoato de isoidida) y un uso de los mismos en el envasado de llenado en caliente Download PDFInfo
- Publication number
- ES2758535T3 ES2758535T3 ES15720080T ES15720080T ES2758535T3 ES 2758535 T3 ES2758535 T3 ES 2758535T3 ES 15720080 T ES15720080 T ES 15720080T ES 15720080 T ES15720080 T ES 15720080T ES 2758535 T3 ES2758535 T3 ES 2758535T3
- Authority
- ES
- Spain
- Prior art keywords
- isoidide
- butanediol
- temperature
- copolyester
- furanoate
- 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
- KLDXJTOLSGUMSJ-UNTFVMJOSA-N (3s,3ar,6s,6ar)-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan-3,6-diol Chemical compound O[C@H]1CO[C@@H]2[C@@H](O)CO[C@@H]21 KLDXJTOLSGUMSJ-UNTFVMJOSA-N 0.000 title claims abstract description 41
- SMNDYUVBFMFKNZ-UHFFFAOYSA-N 2-furoic acid Chemical compound OC(=O)C1=CC=CO1 SMNDYUVBFMFKNZ-UHFFFAOYSA-N 0.000 title claims abstract description 11
- 238000004806 packaging method and process Methods 0.000 title claims description 16
- 229920006344 thermoplastic copolyester Polymers 0.000 title description 3
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims abstract description 24
- 229920001634 Copolyester Polymers 0.000 claims abstract description 20
- CHTHALBTIRVDBM-UHFFFAOYSA-N furan-2,5-dicarboxylic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)O1 CHTHALBTIRVDBM-UHFFFAOYSA-N 0.000 claims abstract description 17
- OWBTYPJTUOEWEK-UHFFFAOYSA-N butane-2,3-diol Chemical compound CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 claims abstract description 12
- 238000006116 polymerization reaction Methods 0.000 claims description 36
- 229920000642 polymer Polymers 0.000 claims description 31
- 239000000155 melt Substances 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 18
- 238000009833 condensation Methods 0.000 claims description 6
- 230000005494 condensation Effects 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 230000008569 process Effects 0.000 claims description 5
- 235000013305 food Nutrition 0.000 claims description 4
- 229920006126 semicrystalline polymer Polymers 0.000 claims description 4
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 claims description 2
- 239000000463 material Substances 0.000 description 23
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 20
- 229920000728 polyester Polymers 0.000 description 15
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 150000002009 diols Chemical class 0.000 description 10
- 229910052757 nitrogen Inorganic materials 0.000 description 10
- 229920000139 polyethylene terephthalate Polymers 0.000 description 10
- 239000005020 polyethylene terephthalate Substances 0.000 description 10
- BYEAHWXPCBROCE-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropan-2-ol Chemical compound FC(F)(F)C(O)C(F)(F)F BYEAHWXPCBROCE-UHFFFAOYSA-N 0.000 description 9
- KLDXJTOLSGUMSJ-JGWLITMVSA-N Isosorbide Chemical compound O[C@@H]1CO[C@@H]2[C@@H](O)CO[C@@H]21 KLDXJTOLSGUMSJ-JGWLITMVSA-N 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 229960002479 isosorbide Drugs 0.000 description 9
- 238000003756 stirring Methods 0.000 description 9
- 230000009477 glass transition Effects 0.000 description 8
- 229920001707 polybutylene terephthalate Polymers 0.000 description 7
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 238000005227 gel permeation chromatography Methods 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 238000001816 cooling Methods 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 229920001169 thermoplastic Polymers 0.000 description 5
- 239000010936 titanium Substances 0.000 description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 238000000113 differential scanning calorimetry Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000011049 filling Methods 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 238000010348 incorporation Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 238000001556 precipitation Methods 0.000 description 4
- 238000002411 thermogravimetry Methods 0.000 description 4
- 239000004416 thermosoftening plastic Substances 0.000 description 4
- DTQVDTLACAAQTR-UHFFFAOYSA-N trifluoroacetic acid Substances OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 238000005481 NMR spectroscopy Methods 0.000 description 3
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 229920001519 homopolymer Polymers 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 229940078552 o-xylene Drugs 0.000 description 3
- 238000002103 osmometry Methods 0.000 description 3
- 239000005022 packaging material Substances 0.000 description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
- 239000004926 polymethyl methacrylate Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- -1 bicyclic diols Chemical class 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 229920000402 bisphenol A polycarbonate polymer Polymers 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 230000001627 detrimental effect Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000001374 small-angle light scattering Methods 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 2
- 238000004736 wide-angle X-ray diffraction Methods 0.000 description 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- AXPZIVKEZRHGAS-UHFFFAOYSA-N 3-benzyl-5-[(2-nitrophenoxy)methyl]oxolan-2-one Chemical compound [O-][N+](=O)C1=CC=CC=C1OCC1OC(=O)C(CC=2C=CC=CC=2)C1 AXPZIVKEZRHGAS-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-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
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-ZXXMMSQZSA-N D-iditol Chemical compound OC[C@@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-ZXXMMSQZSA-N 0.000 description 1
- 238000011993 High Performance Size Exclusion Chromatography Methods 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229920006392 biobased thermoplastic Polymers 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000006210 cyclodehydration reaction Methods 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 231100000507 endocrine disrupting Toxicity 0.000 description 1
- 238000006345 epimerization reaction Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 235000015203 fruit juice Nutrition 0.000 description 1
- 235000012055 fruits and vegetables Nutrition 0.000 description 1
- 239000005431 greenhouse gas Substances 0.000 description 1
- 229920006258 high performance thermoplastic Polymers 0.000 description 1
- 235000021268 hot food Nutrition 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 239000011846 petroleum-based material Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- CUNPJFGIODEJLQ-UHFFFAOYSA-M potassium;2,2,2-trifluoroacetate Chemical compound [K+].[O-]C(=O)C(F)(F)F CUNPJFGIODEJLQ-UHFFFAOYSA-M 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 238000013374 right angle light scattering Methods 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000011496 sports drink Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 238000000870 ultraviolet spectroscopy Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 235000015192 vegetable juice Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/66—Polyesters containing oxygen in the form of ether groups
- C08G63/668—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/672—Dicarboxylic acids and dihydroxy compounds
-
- 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
- C08G63/66—Polyesters containing oxygen in the form of ether groups
-
- 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
- C08G63/78—Preparation processes
-
- 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
- C08G63/78—Preparation processes
- C08G63/80—Solid-state polycondensation
-
- 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
- C08G63/88—Post-polymerisation treatment
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyesters Or Polycarbonates (AREA)
- Wrappers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201461986257P | 2014-04-30 | 2014-04-30 | |
| PCT/EP2015/059555 WO2015166070A1 (en) | 2014-04-30 | 2015-04-30 | Polyisoidide furanoate thermoplastic polyesters and copolyesters and a use thereof in hot fill packaging |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2758535T3 true ES2758535T3 (es) | 2020-05-05 |
Family
ID=53039907
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES15720080T Active ES2758535T3 (es) | 2014-04-30 | 2015-04-30 | Copoliésteres termoplásticos de poli(furanoato de isoidida) y un uso de los mismos en el envasado de llenado en caliente |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US10125216B2 (enExample) |
| EP (1) | EP3137531B1 (enExample) |
| JP (1) | JP6554485B2 (enExample) |
| KR (2) | KR102378006B1 (enExample) |
| CN (1) | CN106471038B (enExample) |
| AU (1) | AU2015254523B2 (enExample) |
| BR (1) | BR112016025235B1 (enExample) |
| CA (1) | CA2946080C (enExample) |
| ES (1) | ES2758535T3 (enExample) |
| MX (1) | MX380350B (enExample) |
| WO (1) | WO2015166070A1 (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6175501B2 (ja) * | 2012-08-31 | 2017-08-02 | ソシエテ アノニム デ ゾ ミネラル デヴィアン エ オン ナブレジェ“エス．ア．ウ．エム．ウ” | ボトルの製造方法 |
| ES2935593T3 (es) | 2015-02-24 | 2023-03-08 | Archer Daniels Midland Co | Fabricación y purificación de isoidida |
| CA3039502A1 (en) * | 2016-10-05 | 2018-04-12 | Furanix Technologies B.V. | Process for the production of a solid-state polymerized poly(tetramethylene-2,5-furan dicarboxylate) polymer and polymer thus produced |
| CN110914335A (zh) * | 2017-05-18 | 2020-03-24 | 阿凡田知识中心有限公司 | 聚酯共聚物 |
| FR3072094B1 (fr) | 2017-10-11 | 2020-09-04 | Roquette Freres | Polyester thermoplastique hautement incorpore en motif 1,4 : 3,6-dianhydro-l-iditol |
| CN108264634B (zh) * | 2018-01-29 | 2021-08-06 | 中国科学院成都有机化学有限公司 | 一种2,5-呋喃二甲酸共聚酯及其制备方法 |
| CN108467479B (zh) * | 2018-05-08 | 2021-07-06 | 成都中科普瑞净化设备有限公司 | 一种增韧2,5-呋喃二甲酸共聚酯 |
| US11447322B2 (en) * | 2019-02-21 | 2022-09-20 | Pepsico, Inc. | Beverage container |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6063464A (en) * | 1998-04-23 | 2000-05-16 | Hna Holdings, Inc. | Isosorbide containing polyesters and methods for making same |
| US7052764B2 (en) * | 2002-12-19 | 2006-05-30 | E. I. Du Pont De Nemours And Company | Shaped articles comprising poly[(trimethylene-co-dianhydrosugar ester) dicarboxylate] or poly(trimethylene-co-dianhydro-dicarboxylate with improved stability |
| BRPI0410573B1 (pt) * | 2003-05-21 | 2015-12-01 | Dak Americas Mississippi Inc | resinas de poliéster de cristalização lenta e o método para a produção das mesmas |
| US20100160548A1 (en) * | 2006-09-15 | 2010-06-24 | Bart Adrianus Johannes Noordover | Process for the production of a dianhydrohexitol based polyester |
| ITMI20080507A1 (it) * | 2008-03-26 | 2009-09-27 | Novamont Spa | Poliestere biodegradabile, suo processo di preparazione e prodotti comprendenti detto poliestere. |
| IT1387503B (it) * | 2008-05-08 | 2011-04-13 | Novamont Spa | Poliestere biodegradabile alifatico-aromatico |
| IT1403611B1 (it) * | 2010-12-22 | 2013-10-31 | Novamont Spa | Composizione di poliesteri |
| JP6046059B2 (ja) * | 2011-03-15 | 2016-12-14 | オセ−テクノロジーズ ビーブイ | バイオ系ポリエステルラテックス |
| KR20120121477A (ko) * | 2011-04-27 | 2012-11-06 | 에스케이케미칼주식회사 | 단단한 폴리(1,4:3,6-디안히드로헥시톨 에스테르) 제조방법 |
| IN2014MN01416A (enExample) * | 2012-01-04 | 2015-04-03 | Pepsico Inc | |
| NZ628958A (en) * | 2012-03-30 | 2016-02-26 | Du Pont | Polyesters and fibers made therefrom |
| NL1039833C2 (en) * | 2012-10-02 | 2014-04-22 | Stichting Dutch Polymeer Inst | Polymer, process for producing such polymer and composition comprising such polymer. |
| JP2016536172A (ja) * | 2013-08-30 | 2016-11-24 | ザ コカ・コーラ カンパニーＴｈｅ Ｃｏｃａ‐Ｃｏｌａ Ｃｏｍｐａｎｙ | フラン酸ポリマーのプリフォーム、容器および加工 |
| FR3020811B1 (fr) * | 2014-05-09 | 2016-06-10 | Roquette Freres | Polyesters aromatiques thermoplastiques comprenant des motifs tetrahydrofuranedimethanol et acide furanedicarboxylique |
-
2015
- 2015-04-30 MX MX2016014215A patent/MX380350B/es unknown
- 2015-04-30 BR BR112016025235-7A patent/BR112016025235B1/pt active IP Right Grant
- 2015-04-30 ES ES15720080T patent/ES2758535T3/es active Active
- 2015-04-30 KR KR1020217009396A patent/KR102378006B1/ko active Active
- 2015-04-30 EP EP15720080.9A patent/EP3137531B1/en active Active
- 2015-04-30 CA CA2946080A patent/CA2946080C/en active Active
- 2015-04-30 WO PCT/EP2015/059555 patent/WO2015166070A1/en not_active Ceased
- 2015-04-30 US US15/304,644 patent/US10125216B2/en active Active
- 2015-04-30 JP JP2016563424A patent/JP6554485B2/ja active Active
- 2015-04-30 CN CN201580022528.1A patent/CN106471038B/zh active Active
- 2015-04-30 AU AU2015254523A patent/AU2015254523B2/en active Active
- 2015-04-30 KR KR1020167032214A patent/KR20170008232A/ko not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| CA2946080C (en) | 2020-11-10 |
| BR112016025235A2 (pt) | 2017-08-15 |
| EP3137531B1 (en) | 2019-10-23 |
| CA2946080A1 (en) | 2015-11-05 |
| KR20170008232A (ko) | 2017-01-23 |
| AU2015254523B2 (en) | 2018-11-29 |
| EP3137531A1 (en) | 2017-03-08 |
| MX2016014215A (es) | 2017-06-06 |
| US10125216B2 (en) | 2018-11-13 |
| BR112016025235B1 (pt) | 2021-07-27 |
| US20170037181A1 (en) | 2017-02-09 |
| KR102378006B1 (ko) | 2022-03-24 |
| AU2015254523A1 (en) | 2016-10-27 |
| CN106471038B (zh) | 2019-12-31 |
| MX380350B (es) | 2025-03-12 |
| KR20210038997A (ko) | 2021-04-08 |
| JP2017514937A (ja) | 2017-06-08 |
| CN106471038A (zh) | 2017-03-01 |
| JP6554485B2 (ja) | 2019-07-31 |
| WO2015166070A1 (en) | 2015-11-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2758535T3 (es) | Copoliésteres termoplásticos de poli(furanoato de isoidida) y un uso de los mismos en el envasado de llenado en caliente | |
| Kim et al. | Sustainable terpolyester of high Tg based on bio heterocyclic monomer of dimethyl furan-2, 5-dicarboxylate and isosorbide | |
| Kang et al. | Synthesis and characterization of biobased isosorbide-containing copolyesters as shape memory polymers for biomedical applications | |
| ES2869249T3 (es) | Procedimiento para la preparación de poli(tereftalato de etileno) modificado con propiedades de barrera, mecánicas y térmicas mejoradas y productos del mismo | |
| KR102210711B1 (ko) | 무수당 알코올과 무수당 알코올-알킬렌 글리콜을 포함하는 생분해성 공중합 폴리에스테르 수지 및 이의 제조 방법 | |
| ES2962764T3 (es) | Procedimiento para preparar poli(furandicarboxilato de trimetileno) | |
| Zhang et al. | Aliphatic–aromatic poly (butylene carbonate‐co‐terephthalate) random copolymers: Synthesis, cocrystallization, and composition‐dependent properties | |
| Zhu et al. | Synthesis of high-Tg fluorinated polyesters based on 2, 5-furandicarboxylic acid | |
| Gagliardi et al. | Chemical synthesis of a biodegradable PEGylated copolymer from ε-caprolactone and γ-valerolactone: evaluation of reaction and functional properties | |
| EP4039724B1 (en) | Polyester resin including diester compound and anhydrosugar alcohol, and method for preparing same | |
| ES2962479T3 (es) | Proceso para preparar poli(furandicarboxilato de alquileno) | |
| US20170037182A1 (en) | Polyester resin, method for manufacturing polyester resin, and coating composition containing polyester resin | |
| ES2880324T3 (es) | Proceso para preparar poli(furandicarboxilato de trimetileno) usando catalizador de zinc | |
| TWI703171B (zh) | 聯苯二甲酸共聚酯及其製法 | |
| Jang et al. | An investigation of novel biodegradable flexible copolyester derived from bio-based isosorbide: Synthesis and characterization of poly (butylene-co-isosorbide sebacate) | |
| Hussain et al. | Synthesis and unique characteristics of biobased high Tg copolyesters with improved performance properties for flexible electronics and packaging applications | |
| CN102918078B (zh) | 乳酸-异山梨醇共聚酯及其制备方法 | |
| JP2017160359A (ja) | ポリテトラメチレングリコール共重合ポリブチレンテレフタレート | |
| KR102589193B1 (ko) | 무수당 알코올과 무수당 알코올계 폴리카보네이트 디올을 포함하는 생분해성 공중합 폴리에스테르 수지 및 이의 제조 방법, 및 이를 포함하는 성형품 | |
| KR102589197B1 (ko) | 무수당 알코올계 폴리카보네이트 디올을 포함하는 생분해성 공중합 폴리에스테르 수지 및 이의 제조 방법, 및 이를 포함하는 성형품 | |
| Chen et al. | Synthesis of Pyrrolidone-Based Copolyesters with Enhanced Glass Transition Temperatures and Abiotic Hydrolysability | |
| lakshmi Prabha et al. | Design, Synthesis and Characterisation of Novel Biodegradable Aliphatic Copolyesters-Poly (ethylene sebacate-co-butylene succinate) and Poly (ethylene sebacate-co-butylene adipate) | |
| Zakharova | Poly (butylene succinate) copolyesters containing cyclic acetalized tartrate units | |
| Lavilla Aguilar | Bio-based polyesters from cyclic monomers derived from carbohydrates |