KR20170008232A - 폴리이소이다이드 푸라노에이트 열가소성 폴리에스테르 및 코폴리에스테르 및 고온 충전 포장에서의 이의 용도 - Google Patents
폴리이소이다이드 푸라노에이트 열가소성 폴리에스테르 및 코폴리에스테르 및 고온 충전 포장에서의 이의 용도 Download PDFInfo
- Publication number
- KR20170008232A KR20170008232A KR1020167032214A KR20167032214A KR20170008232A KR 20170008232 A KR20170008232 A KR 20170008232A KR 1020167032214 A KR1020167032214 A KR 1020167032214A KR 20167032214 A KR20167032214 A KR 20167032214A KR 20170008232 A KR20170008232 A KR 20170008232A
- Authority
- KR
- South Korea
- Prior art keywords
- semi
- butanediol
- crystalline
- melt polymerization
- temperature
- 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.)
- Ceased
Links
- 229920001634 Copolyester Polymers 0.000 title claims abstract description 22
- 238000004806 packaging method and process Methods 0.000 title claims description 9
- SMNDYUVBFMFKNZ-UHFFFAOYSA-N 2-furoic acid Chemical compound OC(=O)C1=CC=CO1 SMNDYUVBFMFKNZ-UHFFFAOYSA-N 0.000 title claims description 6
- 229920000728 polyester Polymers 0.000 title description 20
- 229920001169 thermoplastic Polymers 0.000 title description 4
- 239000004416 thermosoftening plastic Substances 0.000 title description 3
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 45
- 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 27
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims abstract description 18
- 238000009833 condensation Methods 0.000 claims abstract description 10
- OWBTYPJTUOEWEK-UHFFFAOYSA-N butane-2,3-diol Chemical compound CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229920006126 semicrystalline polymer Polymers 0.000 claims abstract description 9
- 230000005494 condensation Effects 0.000 claims abstract description 6
- 239000000155 melt Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 17
- 150000002009 diols Chemical class 0.000 claims description 15
- 230000009477 glass transition Effects 0.000 claims description 9
- 229920001577 copolymer Polymers 0.000 claims description 8
- 239000007787 solid Substances 0.000 claims description 7
- 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 claims description 6
- 238000007711 solidification Methods 0.000 claims description 4
- 235000013305 food Nutrition 0.000 claims description 3
- 230000008569 process Effects 0.000 claims description 3
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 claims description 2
- 230000003606 oligomerizing effect Effects 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 abstract description 28
- 239000000463 material Substances 0.000 abstract description 23
- 238000004519 manufacturing process Methods 0.000 abstract description 8
- 150000002148 esters Chemical class 0.000 abstract description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 20
- 229910052757 nitrogen Inorganic materials 0.000 description 10
- 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
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 229920001519 homopolymer Polymers 0.000 description 9
- 229960002479 isosorbide Drugs 0.000 description 9
- 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 8
- 239000003054 catalyst Substances 0.000 description 8
- 229920000139 polyethylene terephthalate Polymers 0.000 description 8
- 239000005020 polyethylene terephthalate Substances 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000005227 gel permeation chromatography Methods 0.000 description 6
- 229920001707 polybutylene terephthalate Polymers 0.000 description 6
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 238000000113 differential scanning calorimetry Methods 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 239000010936 titanium Substances 0.000 description 5
- 238000004736 wide-angle X-ray diffraction Methods 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- -1 polyethylene terephthalate Polymers 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- 238000002411 thermogravimetry Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 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
- 238000004458 analytical method Methods 0.000 description 3
- 239000010779 crude oil Substances 0.000 description 3
- 238000011049 filling Methods 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
- 238000002103 osmometry Methods 0.000 description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
- 239000004926 polymethyl methacrylate Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 229920005992 thermoplastic resin Polymers 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
- 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 2
- 239000002253 acid Substances 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 125000004429 atom Chemical group 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
- 239000002178 crystalline material Substances 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229940078552 o-xylene Drugs 0.000 description 2
- 238000001556 precipitation Methods 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
- 230000008023 solidification Effects 0.000 description 2
- 239000000243 solution 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
- 238000012360 testing method Methods 0.000 description 2
- 238000001291 vacuum drying Methods 0.000 description 2
- QFZTUWOWMRNMAH-UHFFFAOYSA-N 2h-pyran-2-carboxylic acid Chemical compound OC(=O)C1OC=CC=C1 QFZTUWOWMRNMAH-UHFFFAOYSA-N 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-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
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 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
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 229920013724 bio-based polymer Polymers 0.000 description 1
- 229920006392 biobased thermoplastic Polymers 0.000 description 1
- 229940106691 bisphenol a Drugs 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000006210 cyclodehydration reaction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 230000002124 endocrine Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 239000005431 greenhouse gas Substances 0.000 description 1
- FBPFZTCFMRRESA-UHFFFAOYSA-N hexane-1,2,3,4,5,6-hexol Chemical compound OCC(O)C(O)C(O)C(O)CO FBPFZTCFMRRESA-UHFFFAOYSA-N 0.000 description 1
- 229920006258 high performance thermoplastic Polymers 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 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
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 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
- 239000005022 packaging material Substances 0.000 description 1
- 238000012858 packaging process Methods 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
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 239000002861 polymer material Substances 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
- 230000001376 precipitating effect Effects 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- HKJYVRJHDIPMQB-UHFFFAOYSA-N propan-1-olate;titanium(4+) Chemical compound CCCO[Ti](OCCC)(OCCC)OCCC HKJYVRJHDIPMQB-UHFFFAOYSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000013374 right angle light scattering Methods 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 238000007789 sealing Methods 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
- 229920000576 tactic polymer Polymers 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
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 238000000870 ultraviolet spectroscopy 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
-
- 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
- C08G63/78—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)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020217009396A KR102378006B1 (ko) | 2014-04-30 | 2015-04-30 | 폴리이소이다이드 푸라노에이트 열가소성 폴리에스테르 및 코폴리에스테르 및 고온 충전 포장에서의 이의 용도 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201461986257P | 2014-04-30 | 2014-04-30 | |
| US61/986,257 | 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 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020217009396A Division KR102378006B1 (ko) | 2014-04-30 | 2015-04-30 | 폴리이소이다이드 푸라노에이트 열가소성 폴리에스테르 및 코폴리에스테르 및 고온 충전 포장에서의 이의 용도 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20170008232A true KR20170008232A (ko) | 2017-01-23 |
Family
ID=53039907
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020167032214A Ceased KR20170008232A (ko) | 2014-04-30 | 2015-04-30 | 폴리이소이다이드 푸라노에이트 열가소성 폴리에스테르 및 코폴리에스테르 및 고온 충전 포장에서의 이의 용도 |
| KR1020217009396A Active KR102378006B1 (ko) | 2014-04-30 | 2015-04-30 | 폴리이소이다이드 푸라노에이트 열가소성 폴리에스테르 및 코폴리에스테르 및 고온 충전 포장에서의 이의 용도 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020217009396A Active KR102378006B1 (ko) | 2014-04-30 | 2015-04-30 | 폴리이소이다이드 푸라노에이트 열가소성 폴리에스테르 및 코폴리에스테르 및 고온 충전 포장에서의 이의 용도 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US10125216B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP3137531B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP6554485B2 (cg-RX-API-DMAC7.html) |
| KR (2) | KR20170008232A (cg-RX-API-DMAC7.html) |
| CN (1) | CN106471038B (cg-RX-API-DMAC7.html) |
| AU (1) | AU2015254523B2 (cg-RX-API-DMAC7.html) |
| BR (1) | BR112016025235B1 (cg-RX-API-DMAC7.html) |
| CA (1) | CA2946080C (cg-RX-API-DMAC7.html) |
| ES (1) | ES2758535T3 (cg-RX-API-DMAC7.html) |
| MX (1) | MX380350B (cg-RX-API-DMAC7.html) |
| WO (1) | WO2015166070A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20160009015A1 (en) * | 2012-08-31 | 2016-01-14 | Societe Anonyme Des Eaux Minerales D'evian S.A.E.M.E | Bottle, method of making the same and use of fdca and diol monomers in such bottle |
| ES2935593T3 (es) | 2015-02-24 | 2023-03-08 | Archer Daniels Midland Co | Fabricación y purificación de isoidida |
| WO2018067007A1 (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 produce |
| JP7159213B2 (ja) * | 2017-05-18 | 2022-10-24 | アバンティウム・ナレッジ・センター・ベー・フェー | ポリエステルコポリマー |
| 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 |
| WO2004104080A1 (en) * | 2003-05-21 | 2004-12-02 | Wellman, Inc. | Slow-crystallizing polyester resins |
| JP2010503736A (ja) * | 2006-09-15 | 2010-02-04 | スティッチング ダッチ ポリマー インスティテュート | ジアンヒドロヘキシトールをベースとしたポリエステルの製造方法 |
| 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 |
| US20130171397A1 (en) * | 2012-01-04 | 2013-07-04 | Pepsico, Inc. | 2,5-furan dicarboxylic acid-based polyesters prepared from biomass |
| US20150111450A1 (en) * | 2012-03-30 | 2015-04-23 | E I Du Pont De Nemours And Company | 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. |
| BR112016004364A2 (pt) * | 2013-08-30 | 2020-07-07 | The Coca-Cola Company | Pré-formas de polímeros furanoicos, recipientes e processamento |
| FR3020811B1 (fr) * | 2014-05-09 | 2016-06-10 | Roquette Freres | Polyesters aromatiques thermoplastiques comprenant des motifs tetrahydrofuranedimethanol et acide furanedicarboxylique |
-
2015
- 2015-04-30 CA CA2946080A patent/CA2946080C/en active Active
- 2015-04-30 CN CN201580022528.1A patent/CN106471038B/zh active Active
- 2015-04-30 KR KR1020167032214A patent/KR20170008232A/ko not_active Ceased
- 2015-04-30 KR KR1020217009396A patent/KR102378006B1/ko active Active
- 2015-04-30 EP EP15720080.9A patent/EP3137531B1/en active Active
- 2015-04-30 WO PCT/EP2015/059555 patent/WO2015166070A1/en not_active Ceased
- 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 JP JP2016563424A patent/JP6554485B2/ja active Active
- 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
Also Published As
| Publication number | Publication date |
|---|---|
| WO2015166070A1 (en) | 2015-11-05 |
| MX2016014215A (es) | 2017-06-06 |
| CN106471038B (zh) | 2019-12-31 |
| BR112016025235B1 (pt) | 2021-07-27 |
| CN106471038A (zh) | 2017-03-01 |
| BR112016025235A2 (pt) | 2017-08-15 |
| ES2758535T3 (es) | 2020-05-05 |
| KR102378006B1 (ko) | 2022-03-24 |
| CA2946080C (en) | 2020-11-10 |
| EP3137531A1 (en) | 2017-03-08 |
| US10125216B2 (en) | 2018-11-13 |
| MX380350B (es) | 2025-03-12 |
| JP2017514937A (ja) | 2017-06-08 |
| AU2015254523A1 (en) | 2016-10-27 |
| CA2946080A1 (en) | 2015-11-05 |
| JP6554485B2 (ja) | 2019-07-31 |
| AU2015254523B2 (en) | 2018-11-29 |
| KR20210038997A (ko) | 2021-04-08 |
| US20170037181A1 (en) | 2017-02-09 |
| EP3137531B1 (en) | 2019-10-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR102378006B1 (ko) | 폴리이소이다이드 푸라노에이트 열가소성 폴리에스테르 및 코폴리에스테르 및 고온 충전 포장에서의 이의 용도 | |
| Kim et al. | Sustainable terpolyester of high Tg based on bio heterocyclic monomer of dimethyl furan-2, 5-dicarboxylate and isosorbide | |
| Morales-Huerta et al. | Poly (alkylene 2, 5-furandicarboxylate) s (PEF and PBF) by ring opening polymerization | |
| EP3119831B1 (en) | Polyesters comprising 2,5-furandicarboxylate and saturated diol units having a high glass transition temperature | |
| Kasmi et al. | Synthesis and crystallization of new fully renewable resources-based copolyesters: Poly (1, 4-cyclohexanedimethanol-co-isosorbide 2, 5-furandicarboxylate) | |
| de Ilarduya et al. | Chemical structure and microstructure of poly (alkylene terephthalate) s, their copolyesters, and their blends as studied by NMR | |
| US10077340B2 (en) | Poly(beta-methyl-delta-valerolactone) block polymers | |
| EP4204475B1 (en) | Process for producing polyester comprising 2,5-furandicarboxylate units | |
| US20240166801A1 (en) | Biodegradable copolymer polyester resin comprising anhydrosugar alcohol and anhydrousugar alcohol-alkylene glycol and method for preparing same | |
| WO2013184014A1 (en) | Process for preparing high molecular weight poly(lactic acid) by melt polycondensation | |
| EP4039724B1 (en) | Polyester resin including diester compound and anhydrosugar alcohol, and method for preparing same | |
| Paszkiewicz et al. | Supramolecular structure, relaxation behavior and free volume of bio-based poly (butylene 2, 5-furandicarboxylate)-block-poly (caprolactone) copolyesters | |
| Albanese et al. | The aliphatic counterpart of PET, PPT and PBT aromatic polyesters: effect of the molecular structure on thermo-mechanical properties. | |
| Colonna et al. | Poly (1, 4‐cyclohexylenedimethylene‐1, 4‐cyclohexanedicarboxylate): analysis of parameters affecting polymerization and cis–trans isomerization | |
| CN116601206A (zh) | 用于产生包括2,5-呋喃二羧酸酯单元的聚酯的工艺 | |
| KR20250065313A (ko) | 투명성 및 열적 특성이 개선된 폴리에스테르 및 그 제조방법 | |
| Jansen et al. | The microstructure of poly (butylene terephthalate) copolymers via 13C NMR sequence distribution analysis: Solid-state copolymerization versus melt copolymerization | |
| ES2880324T3 (es) | Proceso para preparar poli(furandicarboxilato de trimetileno) usando catalizador de zinc | |
| Hussain et al. | Synthesis and unique characteristics of biobased high Tg copolyesters with improved performance properties for flexible electronics and packaging applications | |
| 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) | |
| 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 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
Patent event date: 20161118 Patent event code: PA01051R01D Comment text: International Patent Application |
|
| PG1501 | Laying open of application | ||
| PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20200424 Comment text: Request for Examination of Application |
|
| PA0302 | Request for accelerated examination |
Patent event date: 20200424 Patent event code: PA03022R01D Comment text: Request for Accelerated Examination |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20200820 Patent event code: PE09021S01D |
|
| E601 | Decision to refuse application | ||
| PE0601 | Decision on rejection of patent |
Patent event date: 20201229 Comment text: Decision to Refuse Application Patent event code: PE06012S01D Patent event date: 20200820 Comment text: Notification of reason for refusal Patent event code: PE06011S01I |
|
| E601 | Decision to refuse application | ||
| E801 | Decision on dismissal of amendment | ||
| PE0601 | Decision on rejection of patent |
Patent event date: 20210304 Comment text: Decision to Refuse Application Patent event code: PE06012S01D Patent event date: 20200820 Comment text: Notification of reason for refusal Patent event code: PE06011S01I |
|
| PE0801 | Dismissal of amendment |
Patent event code: PE08012E01D Comment text: Decision on Dismissal of Amendment Patent event date: 20210304 Patent event code: PE08011R01I Comment text: Amendment to Specification, etc. Patent event date: 20210128 Patent event code: PE08011R01I Comment text: Amendment to Specification, etc. Patent event date: 20201016 Patent event code: PE08011R01I Comment text: Amendment to Specification, etc. Patent event date: 20200513 Patent event code: PE08011R01I Comment text: Amendment to Specification, etc. Patent event date: 20200424 |
|
| A107 | Divisional application of patent | ||
| PA0104 | Divisional application for international application |
Comment text: Divisional Application for International Patent Patent event code: PA01041R01D Patent event date: 20210330 |