Evaluation of polyesters from renewable resources as alternatives to the current fossil-based polymers. Phase transitions of poly(butylene 2,5-furan-dicarboxylate)

被引:174
作者
Papageorgiou, George Z. [1 ]
Tsanaktsis, Vasilios [1 ]
Papageorgiou, Dimitrios G. [1 ]
Exarhopoulos, Stylianos [2 ]
Papageorgiou, Maria [2 ]
Bikiaris, Dimitrios N. [1 ]
机构
[1] Aristotle Univ Thessaloniki, Dept Chem, Lab Polymer Chem & Technol, GR-54124 Thessaloniki, Macedonia, Greece
[2] Technol Educ Inst Thessaloniki, Dept Food Technol, GR-57400 Thessaloniki, Greece
关键词
Poly(butylene 2,5-furan dicarboxylate); Polyesters; Crystallization; MELTING BEHAVIOR; CRYSTALLIZATION KINETICS; NONISOTHERMAL CRYSTALLIZATION; ENZYMATIC DEGRADATION; BIOBASED POLYESTERS; THERMAL-PROPERTIES; POLY(ETHYLENE-TEREPHTHALATE); FURAN; COPOLYMERS; SUCCINATE);
D O I
10.1016/j.polymer.2014.06.025
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(butylene 2,5-furan dicarboxylate) (PBF) is an alipharomatic polyester that can be prepared using monomers derived from renewable resources such as 2,5-furan dicarboxylic acid and 1,4-butanediol. In the present work the thermal behavior of PBF was studied. Multiple melting was observed during heating traces of samples isothermally crystallized from the melt using differential scanning calorimetry (DSC). The wide angle X-ray diffraction (WAXD) patterns did not reveal the presence of a second crystal population, or a crystal transition upon heating. DSC study showed that the phenomena are closely related to recrystallization. Temperature modulated DSC (TMDSC) tests indeed evidenced enhanced recrystallization. The equilibrium melting point was estimated to be 184.5 degrees C using the linear Hoffman-Weeks extrapolation. The heat of fusion of the pure crystalline polymer was found equal to 120 J/g or (27.35 kJ/mol), a little lower than that of PBT. The Lauritzen-Hoffman secondary nucleation theory was used and the surface energy values and the work of chain folding were found to be comparable to those of PBT, but quite lower than those of poly(ethylene terephthalate) (PET). The non-isothermal crystallization on cooling and the cold-crystallization of quenched samples were also studied. Condensed spherulites were observed on isothermal crystallization under large supercoolings by using polarized optical microscopy (POM), while the spherulites turned to ring-banded morphology at higher temperatures. In every case the nucleation density was high. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3846 / 3858
页数:13
相关论文
共 58 条
[1]   Isothermal and nonisothermal crystallization kinetics of poly(propylene terephthalate) [J].
Achilias, DS ;
Papageorgiou, GZ ;
Karayannidis, GP .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2004, 42 (20) :3775-3796
[2]   CALCULATION OF AVRAMI PARAMETERS FOR HETEROGENEOUS SOLID-STATE REACTIONS USING A MODIFICATION OF KISSINGER METHOD [J].
AUGIS, JA ;
BENNETT, JE .
JOURNAL OF THERMAL ANALYSIS, 1978, 13 (02) :283-292
[3]   Kinetics of phase change I - General theory [J].
Avrami, M .
JOURNAL OF CHEMICAL PHYSICS, 1939, 7 (12) :1103-1112
[4]   Correlation between chemical and solid-state structures and enzymatic hydrolysis in novel biodegradable polyesters. The case of poly(propylene alkanedicarboxylate)s [J].
Bikiaris, Dimitrios N. ;
Papageorgiou, George Z. ;
Giliopoulos, Dimitrios J. ;
Stergiou, Charalampos A. .
MACROMOLECULAR BIOSCIENCE, 2008, 8 (08) :728-740
[5]   On cross- and self-nucleation in seeded crystallization of isotactic poly(1-butene) [J].
Cavallo, Dario ;
Gardella, Lorenza ;
Portale, Giuseppe ;
Mueller, Alejandro J. ;
Alfonso, Giovanni C. .
POLYMER, 2013, 54 (17) :4637-4644
[6]   QUIESCENT POLYMER CRYSTALLIZATION - MODELING AND MEASUREMENTS [J].
CHAN, TW ;
ISAYEV, AI .
POLYMER ENGINEERING AND SCIENCE, 1994, 34 (06) :461-471
[7]   Spherulite growth rates in binary polymer blends [J].
Di Lorenzo, ML .
PROGRESS IN POLYMER SCIENCE, 2003, 28 (04) :663-689
[8]  
Dostal CAWMS, 1988, ENG MAT HDB ENG PLAS
[9]   SELF-NUCLEATION AND RECRYSTALLIZATION OF ISOTACTIC POLYPROPYLENE (ALPHA-PHASE) INVESTIGATED BY DIFFERENTIAL SCANNING CALORIMETRY [J].
FILLON, B ;
WITTMANN, JC ;
LOTZ, B ;
THIERRY, A .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1993, 31 (10) :1383-1393
[10]  
Friedman H.L., 1964, Journal of Polymer Science Part C: Polymer Symposia, V6, P183, DOI DOI 10.1002/POLC.5070060121