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·2350·                            精细化工   FINE CHEMICALS                                  第 36 卷

            缩聚法是主要方法。当前催化剂以有机钛和有机锡                                 comparison  of  thermal  behavior  and  solid  state  structure  with  its
                                                                   terephthalate  and  naphthalate  homologues[J].  Polymer,  2015,  62:
            为主,酶和有机碱是催化剂的研究热点。2,5-呋喃二
                                                                   28-38.
            甲酸聚酯在热学性能(玻璃化转变温度、热稳定性)                            [13]  Zhu  J  H,  Cai  J  L,  Xie  W  C,  et al.  Poly  (butylene  2,5-furan
                                                                   dicarboxylate),  a  biobased  alternative  to  PBT:  synthesis,  physical
            和力学性能(杨氏模量、抗拉强度)上与相应对苯
                                                                   properties,  and  crystal  structure[J].  Macromolecules,  2013,  46(3):
            二甲酸基聚酯接近,2,5-呋喃二甲酸聚酯对 CO 2 、                           796-804.
            O 2 和 H 2 O 的阻隔性优于对苯二甲酸基聚酯,但 2,5-                  [14]  Ma  J  P,  Yu  X  F,  Xu  J,  et al.  Synthesis  and  crystallinity  of  poly
                                                                   (butylene 2,5-furandicarboxylate)[J]. Polymer, 2012, 53(19): 4145-4151.
            呋喃二甲酸聚酯的断裂伸长率较低,不利于后续加                             [15]  Terzopoulou  Z,  Tsanaktsis  V,  Nerantzaki  M,  et al.  Decomposition
            工和应用。为改善 2,5-呋喃二甲酸聚酯的力学和热                              mechanism  of  polyesters  based  on  2,5-furandicarboxylic  acid  and
                                                                   aliphatic  diols  with  medium  and  long  chain  methylene  groups[J].
            学等性能,采取了无机纳米改性、扩链改性和共聚                                 Polymer Degradation and Stability, 2016, 132: 127-136.
            改性这 3 种方法,其中共聚是最有效的办法。然而,                          [16]  Tsanaktsis V, Terzopoulou Z, Nerantzaki M, et al. New poly (pentylene
                                                                   furanoate) and poly (heptylene furanoate) sustainable polyesters from
            目前的共聚改性单体中只有 1,4-环己烷二甲醇可以                              diols  with  odd  methylene  groups[J].  Materials  Letters,  2016,  178:
            取得较好的综合改性效果。柔性适中的共聚单体是                                 64-67.
                                                               [17]  Tsanaktsis V, Papageorgiou G Z, Bikiaris D N. A facile  method to
            2,5-呋喃二甲酸聚酯共聚改性成功的关键。可以预
                                                                   synthesize  high-molecular-weight  biobased  polyesters  from  2,5-
            见,一旦 2,5-呋喃二甲酸基共聚物的热学、热稳定                              furandicarboxylic  acid  and  long-chain  diols[J].  Journal  of  Polymer
            性、力学性能和气体阻隔性能达到相应对苯二甲酸                                 Science, Part A: Polymer Chemistry, 2015, 53(22): 2617-2632.
                                                               [18]  Terzopoulou Z, Tsanaktsis V, Nerantzaki M, et al. Thermal degradation
            基聚酯的水平,就可实现生物基聚酯替代石油基聚                                 of  biobased  polyesters:  Kinetics  and  decomposition  mechanism  of
            酯达到绿色可持续的目标。                                           polyesters from  2,5-furandicarboxylic acid  and  long-chain  aliphatic
                                                                   diols[J].  Journal  of  Analytical  and  Applied  Pyrolysis,  2016,  117:
                                                                   162-175.
            参考文献:
                                                               [19]  Soares M J, Dannecker P K, Vilela C, et al. Poly (1,20-eicosanediyl
            [1]   Werpy T A, Holladay J E, White J F. Top value added chemicals from   2,5-furandicarboxylate),  a  biodegradable  polyester  from  renewable
                 biomass I. results of screening for potential candidates from sugars   resources[J]. European Polymer Journal, 2017, 90: 301-311.
                 and synthesis gas[R]. Synthetic Fuels, 2004: 1-67.     [20]  van  Berkel  J  G,  Guigo  N,  Visser  H  A,  et al.  Chain  structure  and
            [2]   Zhou Jiadong (周佳栋), Cao Fei (曹飞), Yu Zuolong (余作龙), et al.   molecular  weight  dependent  mechanics  of  poly  (ethylene  2,
                 Research  progress  in  preparation  and  application  of  bio-based  2,   5-furandicarboxylate)  compared  to  poly  (ethylene  terephthalate)[J].
                 5-furandicarboxylic acid as polyester monomer[J]. Acta Polymerica   Macromolecules, 2018, 51(21): 8539-8549.
                 Sinica (高分子学报) , 2016, (1): 1-13.             [21]  Gubbels E, Jasinska-Walc L, Koning C E. Synthesis and characterization
            [3]   Tong  X  L,  Ma  Y,  Li  Y  D.  Biomass  into  chemicals:  Conversion of   of  novel  renewable  polyesters  based  on  2,5-furandicarboxylic  acid
                 sugars  to  furan  derivatives  by  catalytic  processes[J].  Applied   and 2,3-butanediol[J]. Journal of Polymer Science, Part  A-Polymer
                 Catalysis A: General, 2010, 385(1/2): 1-13.       Chemistry, 2013, 51(4): 890-898.
            [4]   James G N D, James L. Improvements in polymers: GB621971[P].   [22]  Wu L L, Mascal M, Farmer T J, et al. Electrochemical coupling of
                 1946-11-12.                                       biomass-derived acids: New C-8 platforms for renewable polymers
            [5]   Gandini A, Silvestre A J D, Neto C P, et al. The furan counterpart of   and fuels[J]. Chemsuschem, 2017, 10(1): 166-170.
                 poly  (ethylene  terephthalate):  An  alternative  material  based  on   [23]  Terzopoulou  Z,  Kasmi  N,  Tsanaktsis  V,  et al.  Synthesis  and
                 renewable resources[J]. Journal of Polymer Science, Part A: Polymer   characterization  of  bio-based  polyesters:  Poly  (2-methyl-1,3-
                 Chemistry, 2009, 47(1): 295-298.                  propylene-2,5-furanoate),  poly  (isosorbide-2,5-furanoate),  poly
            [6]   Gandini  A.  Furans  as  offspring  of  sugars  and  polysaccharides  and   (1,4-cyclohexanedimethylene-2,5-furanoate)[J].  Materials  (Basel),
                                                                   2017, 10(7): 801-820.
                 progenitors of a family of remarkable polymers: A review of recent   [24]  Tsanaktsis  V,  Terzopoulou  Z,  Exarhopoulos  S,  et al.  Sustainable,
                 progress[J]. Polymer Chemistry, 2010, 1(3): 245-251.
            [7]   Gomes  M,    Gandini  A,  Silvestre  A  J  D,  et al.  Synthesis  and   eco-friendly  polyesters  synthesized  from  renewable  resources:
                                                                   Preparation and thermal characteristics of poly (dimethyl-propylene
                 characterization  of  poly  (2,  5-furan  dicarboxylate)s  based  on  a   furanoate)[J]. Polymer Chemistry, 2015, 6(48): 8284-8296.
                 variety  of  diols[J].  Journal  of  Polymer  Science,  Part  A:  Polymer   [25]  Moore  J  A, Kelly J E K.  Polyesters derived from  furan  and
                 Chemistry, 2011, 49(17): 3759-3768.               tetrahydrofuran nuclei[J]. Macromolecules, 1978, 11(3): 568-573.
            [8]   Eerhart A J J E, Faaij A P C, Patel M K. Replacing fossil based PET   [26]  Kanetaka  Y,  Yamazaki  S,  Kimura  K.  High  performance  polyesters
                 with  biobased  PEF;  process  analysis,  energy  and  GHG  balance[J].   prepared  from  bio‐based  2,5‐furandicarboxylic  acid[J].  Journal  of
                 Energy & Environmental Science, 2012, 5(4): 6407-6422.     Fiber Science and Technology, 2016, 72(2): 54-60.
            [9]   Yu  Z  L,  Cao  F,  Zhang  Q  G,  et al.  Synthesis,  characterization  and   [27]  Moore  J  A,  Kelly  J  E.  Polyhydroxymethylfuroate[poly  (2,5-
                 thermal properties of bio-based poly (ethylene 2,5-furan dicarboxylate)   furandiylcarbonyloxymethylene)][J].  Journal  of  Polymer  Science,
                 [J]. Journal of Macromolecular Science,Part B-Physics, 2016, 55(12):   Part A-Polymer Chemistry, 1984, 22(3): 863-864.
                 1135-1145.                                    [28]  Storbeck R, Ballauff M. Synthesis and properties of polyesters based
            [10]  Wu  J  P, Xie H Z,  Wu L B,  et al.  DBU-catalyzed  biobased  poly   on  2,5-furandicarboxylic  acid  and  1,4/3,6-dianhydrohexitols[J].
                 (ethylene 2,5-furandicarboxylate) polyester with rapid melt crystallization:   Polymer, 1993, 34(23): 5003-5006.
                 synthesis, crystallization kinetics and melting behavior[J]. RSC Adv,   [29]  Gopalakrishnan P, Narayan-Sarathy S, Ghosh T, et al. Synthesis and
                 2016, 6(103): 101578-101586.                      characterization  of  bio-based  furanic  polyesters[J].  Journal  of
            [11]  Vannini M, Marchese P, Celli A, et al. Fully biobased poly (propylene   Polymer Research, 2013, 21(1): 340-349.
                 2,5-furandicarboxylate) for packaging applications: Excellent barrier   [30]  Wu  J,  Eduard  P,  Thiyagarajan  S,  et al.  Semi-aromatic  polyesters
                 properties  as  a  function  of  crystallinity[J].  Green  Chemistry,  2015,   based on a carbohydrate-derived rigid diol for engineering plastics[J].
                 17(8): 4162-4166.                                 Chem Sus Chem, 2015, 8(1): 67-72.
            [12]  Papageorgiou G Z, Papageorgiou D G, Tsanaktsis V, et al. Synthesis   [31]  Matos M, Sousa A F, Silvestre A J D. Improving the thermal properties
                 of the bio-based polyester poly (propylene 2,5-furan dicarboxylate).   of  poly  (2,5-furandicarboxylate)s  using  cyclohexylene  moieties: A
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