Nonisothermal crystallization kinetics and thermomechanical properties of multiwalled carbon nanotube-reinforced poly(ε-caprolactone) composites

被引:32
作者
Xu, Guoyong [1 ,2 ]
Du, Longchao [3 ]
Wang, Hu [1 ]
Xia, Ru [3 ]
Meng, Xiangchun [1 ]
Zhu, Qingren [4 ]
机构
[1] Anhui Univ, Ctr Modern Expt Technol, Hefei 230039, Peoples R China
[2] Anhui Zhongding Share Co Ltd, Ningguo 242300, Peoples R China
[3] Anhui Univ, Sch Chem & Chem Engn, Hefei 230039, Peoples R China
[4] Univ Sci & Technol China, Chinese Acad Sci, Struct Res Lab, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China
关键词
carbon nanotubes; poly (epsilon-caprolactone); mechanical properties; nonisothermal crystallization;
D O I
10.1002/pi.2448
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
BACKGROUND: The technological development of poly (e-caprolactone) (PCL) is limited by its short useful lifespan, low modulus and high crystallinity. There are a few papers dealing with the crystallization behavior of carbon nanotube-reinforced PCL composites. However, little work has been done on the crystallization kinetics of melt-compounded PCL/multiwalled carbon nanotube (MWNT) nanocomposites. In this study, PCL/MWNT nanocomposites were successfully prepared by a simple melt-compounding method, and their morphology and mechanical properties as well as their crystallization kinetics were studied. RESULTS: The MWNTs were observed to be homogeneously dispersed throughout the PCL matrix. The incorporation of a very small quantity of MWNTs significantly improved the storage modulus and loss modulus of the PCL/MWNT nanocomposites. The nonisothermal crystallization behavior of the PCL/MWNT nanocomposites exhibits strong dependencies of the degree of crystallinity (X-c), peak crystallization temperature (T-p), half-time of crystallization (t(1/2)) and Avrami exponent (n) on the MWNT content and cooling rate. The MWNTs in the PCL/MWNT nanocomposites exhibit a higher nucleation activity. The crystallization activation energy (E-a) calculated with the Kissinger model is higher when a small amount of MWNTs is added, then gradually decreases; all the E-a values are higher than that of pure PCL. CONCLUSION: This paper reports for the first time the preparation of high-performance biopolymer PCL/MWNT nanocomposites prepared by a simple melt-compounding method. The results show that the PCL/MWNT nanocomposites can broaden the applications of PCL. (C) 2008 Society of Chemical Industry.
引用
收藏
页码:1052 / 1066
页数:15
相关论文
共 77 条
[1]  
Ago H, 1999, ADV MATER, V11, P1281, DOI 10.1002/(SICI)1521-4095(199910)11:15<1281::AID-ADMA1281>3.0.CO
[2]  
2-6
[3]  
Ajayan PM, 2000, ADV MATER, V12, P750, DOI 10.1002/(SICI)1521-4095(200005)12:10<750::AID-ADMA750>3.0.CO
[4]  
2-6
[5]   ALIGNED CARBON NANOTUBE ARRAYS FORMED BY CUTTING A POLYMER RESIN-NANOTUBE COMPOSITE [J].
AJAYAN, PM ;
STEPHAN, O ;
COLLIEX, C ;
TRAUTH, D .
SCIENCE, 1994, 265 (5176) :1212-1214
[6]   Constrained crystallization and activity of filler in surface modified talc polypropylene composites [J].
Alonso, M ;
Velasco, JI ;
deSaja, JA .
EUROPEAN POLYMER JOURNAL, 1997, 33 (03) :255-262
[7]   DC and AC conductivity of carbon nanotubes-polyepoxy composites [J].
Barrau, S ;
Demont, P ;
Peigney, A ;
Laurent, C ;
Lacabanne, C .
MACROMOLECULES, 2003, 36 (14) :5187-5194
[8]   Computational aspects of kinetic analysis Part A: The ICTAC kinetics project-data, methods and results [J].
Brown, ME ;
Maciejewski, M ;
Vyazovkin, S ;
Nomen, R ;
Sempere, J ;
Burnham, A ;
Opfermann, J ;
Strey, R ;
Anderson, HL ;
Kemmler, A ;
Keuleers, R ;
Janssens, J ;
Desseyn, HO ;
Li, CR ;
Tang, TB ;
Roduit, B ;
Malek, J ;
Mitsuhashi, T .
THERMOCHIMICA ACTA, 2000, 355 (1-2) :125-143
[9]   Reinforcement of polymers with carbon nanotubes:: The role of nanotube surface area [J].
Cadek, M ;
Coleman, JN ;
Ryan, KP ;
Nicolosi, V ;
Bister, G ;
Fonseca, A ;
Nagy, JB ;
Szostak, K ;
Béguin, F ;
Blau, WJ .
NANO LETTERS, 2004, 4 (02) :353-356
[10]   A new method to determine the Avrami exponent by dsc studies of non-isothermal crystallization from the molten state [J].
Caze, C ;
Devaux, E ;
Crespy, A ;
Cavrot, JP .
POLYMER, 1997, 38 (03) :497-502