Page 23 - 精细化工2019年第12期
P. 23
第 12 期 王贤松,等: 生物基 2,5-呋喃二甲酸聚酯的研究进展 ·2351·
comparative study[J]. Macromolecular Chemistry and Physics, 2017, [50] Wu B S, Xu Y T, Bu Z Y, et al. Biobased poly (butylene
218(5): 1600492-1600502. 2,5-furandicarboxylate) and poly (butylene adipate-co-butylene
[32] Wang J G, Liu X Q, Zhang Y J, et al. Modification of poly (ethylene 2,5-furandicarboxylate)s: From synthesis using highly purified
2,5-furandicarboxylate) with 1,4-cyclohexanedimethylene: Influence 2,5-furandicarboxylic acid to thermo-mechanical properties[J].
of composition on mechanical and barrier properties[J]. Polymer, Polymer, 2014, 55(16): 3648-3655.
2016, 103: 1-8. [51] Burgess S K, Kriegel R M, Koros W J. Carbon dioxide sorption and
[33] Hong S, Min K D, Nam B U, et al. High molecular weight bio transport in amorphous poly (ethylene furanoate)[J]. Macromolecules,
furan-based co-polyesters for food packaging applications: Synthesis, 2015, 48(7): 2184-2193.
characterization and solid-state polymerization[J]. Green Chemistry, [52] Burgess S K, Mikkilineni D S, Yu D B, et al. Water sorption in poly
2016, 18(19): 5142-5150. (ethylene furanoate) compared to poly (ethylene terephthalate). part
[34] Diao L C, Su K M, Li Z H, et al. Furan-based co-polyesters with 2: kinetic sorption[J]. Polymer, 2014, 55(26): 6870-6882.
enhanced thermal properties: Poly (1,4-butylene-co-1,4- [53] Burgess S K, Karvan O, Johnson J R, et al. Oxygen sorption and
cyclohexanedimethylene-2,5-furandicarboxylic acid)[J]. RSC Adv, transport in amorphous poly (ethylene furanoate)[J]. Polymer, 2014,
2016, 6(33): 27632-27639. 55(18): 4748-4756.
[35] Hachihama Y, Shono T, Hyono K. Syntheses of polyesters containing [54] de Jong E, Dam M A, Sipos L, et al. Furandicarboxylic acid (FDCA),
a furan ring[J]. Technology Reports of the Osaka University, 1958, 8: a versatile building block for a very interesting class of polyesters[J].
475-480. ACS Symposium Series, 2012, 1105(13): 1-13.
[36] Jiang M, Liu Q, Zhang Q, et al. A series of furan-aromatic polyesters [55] Papageorgiou G Z, Tsanaktsis V, Bikiaris D N. Synthesis of poly
synthesized via direct esterification method based on renewable (ethylene furandicarboxylate) polyester using monomers derived
resources[J]. Journal of Polymer Science, Part A: Polymer Chemistry, from renewable resources: thermal behavior comparison with PET
2012, 50(5): 1026-1036. and PEN[J]. Phys Chem Chem Phys, 2014, 16(17): 7946-7958.
[37] Knoop R J I, Vogelzang W, van Haveren J, et al. High molecular [56] Burgess S K, Leisen J E, Kraftschik B E, et al. Chain mobility,
weight poly (ethylene-2,5-furanoate), critical aspects in synthesis and thermal, and mechanical properties of poly (ethylene furanoate)
mechanical property determination[J]. Journal of Polymer Science, compared to poly (ethylene terephthalate)[J]. Macromolecules, 2014,
Part A: Polymer Chemistry, 2013, 51(19): 4191-4199. 47(4): 1383-1391.
[38] Jiang Y, Woortman A J J, Alberda van Ekenstein G O R, et al. A [57] Gert-Jan M, Gruter L S, Matheus A D. Accelerating research into
biocatalytic approach towards sustainable furanic–aliphatic polyesters bio-based FDCA-polyesters by using small scale parallel film
[J]. Polymer Chemistry, 2015, 6(29): 5198-5211. reactors[J]. Combinatorial Chemistry & High Throughput Screening,
[39] Martino L, Niknam V, Guigo N, et al. Morphology and thermal 2012, 15(2): 180-188.
properties of novel clay-based poly (ethylene 2,5-furandicarboxylate) [58] Pfister D, Storti G, Tancini F, et al. Synthesis and ring-opening
(PEF) nanocomposites[J]. RSC Adv, 2016, 6(64): 59800-59807. polymerization of cyclic butylene 2,5-furandicarboxylate[J].
[40] Stoclet G, Gobius du S G, Yeniad B, et al. Isothermal crystallization Macromolecular Chemistry and Physics, 2015, 216(21): 2141-2146.
and structural characterization of poly (ethylene-2,5-furanoate)[J]. [59] Laszlo Sipos. Process for preparing a polymer having a
Polymer, 2015, 72: 165-176. 2,5-furandicarboxylate moiety within the polymer backone and such
[41] Carlos M H J, Martínez de Ilarduya A, Muñoz-Guerra S. Poly (co) polymers: US20160312008[P]. 2016-10-27.
(alkylene 2,5-furandicarboxylate)s (PEF and PBF) by ring opening [60] Terzopoulou Z, Karakatsianopoulou E, Kasmi N, et al. Effect of
polymerization[J]. Polymer, 2016, 87: 148-158. catalyst type on recyclability and decomposition mechanism of poly
[42] Lotti N, Munari A, Gigli M, et al. Thermal and structural response of (ethylene furanoate) biobased polyester[J]. Journal of Analytical and
in situ prepared biobased poly (ethylene 2,5-furan dicarboxylate) Applied Pyrolysis, 2017, 126: 357-370.
nanocomposites[J]. Polymer, 2016, 103: 288-298. [61] Maniar D, Jiang Y, Woortman A J J, et al. Furan-based copolyesters
[43] Papageorgiou G Z, Tsanaktsis V, Papageorgiou D G, et al. Evaluation from renewable resources: Enzymatic synthesis and properties[J].
of polyesters from renewable resources as alternatives to the current Chem Sus Chem, 2019, 12(5): 990-999.
fossil-based polymers. phase transitions of poly (butylene 2,5-furan- [62] Aparaschivei D, Todea A, Frissen A E, et al. Enzymatic synthesis and
dicarboxylate)[J]. Polymer, 2014, 55(16): 3846-3858. characterization of novel terpolymers from renewable sources[J].
[44] Papageorgiou G Z, Tsanaktsis V, Papageorgiou D G, et al. Furan- Pure and Applied Chemistry, 2019, 91(3): 397-408.
based polyesters from renewable resources: Crystallization and [63] Cruz-Izquierdo A, van den Broek L A M, Serra J L, et al.
thermal degradation behavior of poly (hexamethylene 2,5-furan- Lipase-catalyzed synthesis of oligoesters of 2,5-furandicarboxylic
dicarboxylate)[J]. European Polymer Journal, 2015, 67: 383-396. acid with aliphatic diols[J]. Pure and Applied Chemistry, 2015, 87(1):
[45] Papageorgiou G Z, Guigo N, Tsanaktsis V, et al. On the bio-based 59-69.
furanic polyesters: Synthesis and thermal behavior study of poly [64] Cao Xiaoyu (曹小玉), Li Yuanyuan (李圆圆), Li Yue (李跃), et al.
(octylene furanoate) using fast and temperature modulated scanning Chain extension of poly (ethylene 2,5-furandicarboxylate) by
calorimetry[J]. European Polymer Journal, 2015, 68: 115-127. diisocyanate[J]. Polymeric Materials Science and Engineering (高分
[46] Tsanaktsis V, Bikiaris D N, Guigo N, et al. Synthesis, properties and 子材料科学与工程), 2017, 33(1): 1-6.
thermal behavior of poly (decylene-2,5-furanoate): A biobased [65] Terzopoulou Z, Tsanaktsis V, Bikiaris D N, et al. Biobased poly
polyester from 2,5-furan dicarboxylic acid[J]. RSC Adv, 2015, 5(91): (ethylene furanoate-co-ethylene succinate) copolyesters: Solid state
74592-74604. structure, melting point depression and biodegradability[J]. RSC
[47] Papageorgiou G Z, Guigo N, Tsanaktsis V, et al. Fast crystallization Adv, 2016, 6(87): 84003-84015.
and melting behavior of a long-spaced aliphatic furandicarboxylate [66] Lomelí-Rodríguez M, Martín-Molina M, Jiménez-Pardo M, et al.
biobased polyester, poly (dodecylene 2,5-furanoate)[J]. Industrial & Synthesis and kinetic modeling of biomass-derived renewable
Engineering Chemistry Research, 2016, 55(18): 5315-5326. Polyesters[J]. Journal of Polymer Science, Part A: Polymer Chemistry,
[48] Wang J G, Liu X Q, Jia Z, et al. Synthesis of bio-based poly (ethylene 2016, 54(18): 2876-2887.
2,5-furandicarboxylate) copolyesters: higher glass transition temperature, [67] Yu Z L, Zhou J D, Cao F, et al. Chemosynthesis and characterization
better transparency, and good barrier properties[J]. Journal of Polymer of fully biomass-based copolymers of ethylene glycol, 2,5-
Science, Part A: Polymer Chemistry, 2017, 55(19): 3298-3307. furandicarboxylic acid, and succinic acid[J]. Journal of Applied
[49] Wu L, Mincheva R, Xu Y, et al. High molecular weight poly Polymer Science, 2013, 130(2): 1415-1420.
(butylene succinate-co-butylene furandicarboxylate) copolyesters: [68] Hu H, Zhang R Y, Wang J G, et al. Fully bio-based poly (propylene
from catalyzed polycondensation reaction to thermomechanical succinate-co-propylene furandicarboxylate) copolyesters with proper
properties[J]. Biomacromolecules, 2012, 13(9): 2973-2981. mechanical, degradation and barrier properties for green packaging