Bio-based PBT copolyesters derived from D-glucose: influence of composition on properties

被引:62
作者
Japu, Cristina [1 ]
Martinez de Ilarduya, Antxon [1 ]
Alla, Abdelilah [1 ]
Gracia Garcia-Martin, Ma [2 ]
Galbis, Juan A. [2 ]
Munoz-Guerra, Sebastian [1 ]
机构
[1] Univ Politecn Cataluna, ETSEIB, E-08028 Barcelona, Spain
[2] Univ Seville, Fac Farm, E-41012 Seville, Spain
关键词
POLY(BUTYLENE TEREPHTHALATE); SUCCINIC ACID; POLYESTERS; ISOSORBIDE; GALACTITOL; FUTURE;
D O I
10.1039/c3py01425h
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Two series of bio-based PBT copolyesters were obtained by polycondensation in the melt of 2,4: 3,5-di-Omethylene-D-glucitol (Glux-diol) or dimethyl 2,4: 3,5-di-O-methylene-D-glucarate (Glux-diester) with 1,4-butanediol and dimethyl terephthalate. The glucose-based bicyclic compounds used as comonomers were synthesized from commercially available 1,5-D-gluconolactone. The prepared PBT copolyesters had weight-average molecular weights in the 30 000-50 000 range; they had a random microstructure, and they were stable above 300 degrees C. The copolyesters containing less than 30% of sugar-based units were semicrystalline and were found to adopt the triclinic structure of PBT. These copolyesters with low contents in Glux were able to crystallize from the melt but at lower rates than PBT. The T-g value of PBT steadily increased with the incorporation of Glux units in the polyester chain with an increasing ratio of similar to 1.7 degrees C or similar to 1 degrees C per % Glux point, depending on which unit, the diol or the diacid, was replaced. The copolyesters hydrolyzed at higher rates than PBT, and those containing glucarate units displayed an appreciable susceptibility towards biodegradation.
引用
收藏
页码:3190 / 3202
页数:13
相关论文
共 27 条
[1]   Technology development for the production of biobased products from biorefinery carbohydrates-the US Department of Energy's "Top 10" revisited [J].
Bozell, Joseph J. ;
Petersen, Gene R. .
GREEN CHEMISTRY, 2010, 12 (04) :539-554
[2]  
Burk MJ, 2010, INT SUGAR J, V112, P30
[3]   Cyclic and noncyclic polycarbonates of isosorbide (1,4:3,6-dianhydro-D-glucitol) [J].
Chatti, Saber ;
Schwarz, Gert ;
Kricheldorf, Hans R. .
MACROMOLECULES, 2006, 39 (26) :9064-9070
[4]   Plastics Derived from Biological Sources: Present and Future: A Technical and Environmental Review [J].
Chen, Guo-Qiang ;
Patel, Martin K. .
CHEMICAL REVIEWS, 2012, 112 (04) :2082-2099
[5]   Synthesis and radiocarbon evidence of terephthalate polyesters completely prepared from renewable resources [J].
Colonna, Martino ;
Berti, Corrado ;
Fiorini, Maurizio ;
Binassi, Enrico ;
Mazzacurati, Marzia ;
Vannini, Micaela ;
Karanam, Sreepadaraj .
GREEN CHEMISTRY, 2011, 13 (09) :2543-2548
[6]   Polymers from renewable 1,4:3,6-dianhydrohexitols (isosorbide, isomannide and isoidide): A review [J].
Fenouillot, F. ;
Rousseau, A. ;
Colomines, G. ;
Saint-Loup, R. ;
Pascault, J. -P. .
PROGRESS IN POLYMER SCIENCE, 2010, 35 (05) :578-622
[7]   Synthetic Polymers from Readily Available Monosaccharides [J].
Galbis, J. A. ;
Garcia-Martin, M. G. .
CARBOHYDRATES IN SUSTAINABLE DEVELOPMENT II: A MINE FOR FUNCTIONAL MOLECULES AND MATERIALS, 2010, 295 :147-176
[8]  
Gandini A., 2008, MONOMERS POLYM COMPO, P89
[9]   Materials from renewable resources based on furan monomers and furan chemistry: work in progress [J].
Gandini, Alessandro ;
Coelho, Dora ;
Gomes, Monica ;
Reis, Bruno ;
Silvestre, Armando .
JOURNAL OF MATERIALS CHEMISTRY, 2009, 19 (45) :8656-8664
[10]   Polymers from Renewable Resources: A Challenge for the Future of Macromolecular Materials [J].
Gandini, Alessandro .
MACROMOLECULES, 2008, 41 (24) :9491-9504