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 PDF

Info

Publication number: ES2758535T3
Authority: ES; Spain
Prior art keywords: isoidide; butanediol; temperature; copolyester; furanoate
Prior art date: 2014-04-30
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

Application number

ES15720080T

Other languages

English (en)

Spanish (es)

Inventor

Haveren Jacobus Van

Johannes Rutger Idsard Knoop

Es Daniel S Van

Willem Vogelzang

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Wageningen Universiteit

Original Assignee

Wageningen Universiteit

Priority date (The priority date 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 date listed.)

2014-04-30

Filing date

2015-04-30

Publication date

2020-05-05

2015-04-30 Application filed by Wageningen Universiteit filed Critical Wageningen Universiteit

2020-05-05 Application granted granted Critical

2020-05-05 Publication of ES2758535T3 publication Critical patent/ES2758535T3/es

Status Active legal-status Critical Current

2035-04-30 Anticipated expiration legal-status Critical

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)

ES15720080T 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 Active ES2758535T3 (es)

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 (2)
EP (1)	EP3137531B1 (2)
JP (1)	JP6554485B2 (2)
KR (2)	KR102378006B1 (2)
CN (1)	CN106471038B (2)
AU (1)	AU2015254523B2 (2)
BR (1)	BR112016025235B1 (2)
CA (1)	CA2946080C (2)
ES (1)	ES2758535T3 (2)
MX (1)	MX380350B (2)
WO (1)	WO2015166070A1 (2)

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CN104703776A (zh) *	2012-08-31	2015-06-10	依云矿泉水股份有限公司	瓶、其制造方法以及fdca和二醇单体在该瓶中的用途
ES2935593T3 (es)	2015-02-24	2023-03-08	Archer Daniels Midland Co	Fabricación y purificación de isoidida
CN109952335B (zh) *	2016-10-05	2021-11-05	福兰尼克斯科技公司	固态聚合的聚(四亚甲基-2,5-呋喃二羧酸酯)聚合物的制备方法及由此制备的聚合物
EP3625284B1 (en) *	2017-05-18	2025-05-07	Avantium Knowledge Centre B.V.	Polyester copolymer
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

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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
MXPA05012617A (es) *	2003-05-21	2006-02-08	Wellman Inc	Resinas de poliester de cristalizacion lenta.
CN101535372A (zh) *	2006-09-15	2009-09-16	斯蒂茨丁荷兰聚合物学会	基于二失水己糖醇的聚酯的制备方法
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
KR20140049516A (ko) *	2011-03-15	2014-04-25	오세-테크놀로지스 베파우	바이오-기재 폴리에스테르 라텍스
KR20120121477A (ko) *	2011-04-27	2012-11-06	에스케이케미칼주식회사	단단한 폴리(1,4:3,6-디안히드로헥시톨 에스테르) 제조방법
CN104379631A (zh) *	2012-01-04	2015-02-25	百事可乐公司	由生物质制备得到的2,5-呋喃二羧酸基聚酯
PL2831317T3 (pl) *	2012-03-30	2021-10-04	Dupont Industrial Biosciences Usa, Llc	Poliestry oraz wykonane z nich włókna
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ＴｈｅＣｏｃａ‐ＣｏｌａＣｏｍｐａｎｙ	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 AU AU2015254523A patent/AU2015254523B2/en active Active
- 2015-04-30 US US15/304,644 patent/US10125216B2/en active Active
- 2015-04-30 CN CN201580022528.1A patent/CN106471038B/zh active Active
- 2015-04-30 BR BR112016025235-7A patent/BR112016025235B1/pt active IP Right Grant
- 2015-04-30 MX MX2016014215A patent/MX380350B/es unknown
- 2015-04-30 CA CA2946080A patent/CA2946080C/en active Active
- 2015-04-30 ES ES15720080T patent/ES2758535T3/es active Active
- 2015-04-30 JP JP2016563424A patent/JP6554485B2/ja 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 KR KR1020167032214A patent/KR20170008232A/ko not_active Ceased
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Publication number	Publication date
MX2016014215A (es)	2017-06-06
AU2015254523B2 (en)	2018-11-29
CA2946080C (en)	2020-11-10
EP3137531B1 (en)	2019-10-23
BR112016025235B1 (pt)	2021-07-27
KR102378006B1 (ko)	2022-03-24
EP3137531A1 (en)	2017-03-08
MX380350B (es)	2025-03-12
JP6554485B2 (ja)	2019-07-31
CA2946080A1 (en)	2015-11-05
BR112016025235A2 (pt)	2017-08-15
US10125216B2 (en)	2018-11-13
KR20210038997A (ko)	2021-04-08
US20170037181A1 (en)	2017-02-09
CN106471038A (zh)	2017-03-01
CN106471038B (zh)	2019-12-31
KR20170008232A (ko)	2017-01-23
WO2015166070A1 (en)	2015-11-05
JP2017514937A (ja)	2017-06-08
AU2015254523A1 (en)	2016-10-27

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