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

Polymer International - Tập 57 Số 9 - Trang 1052-1066 - 2008
Guoyong Xu1,2, Longchao Du3, Hu Wang2, Ru Xia3, Xiangchun Meng2, Qingren Zhu4
1Anhui Zhongding Share Co. Ltd, Ningguo 242300, People's Republic of China
2Center of Modern Experimental Technology, Anhui University, Hefei 230039, People’s Republic of China
3School of Chemistry & Chemical Engineering, Anhui University, Hefei 230039, People's Republic of China
4Hefei National Laboratory for Physical Sciences at the Microscale, Structure Research Laboratory, University of Science and Technology of China, Chinese Academy of Sciences, Hefei 230026, People's Republic of China

Tóm tắt

AbstractBACKGROUND: The technological development of poly(ε‐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 (Xc), peak crystallization temperature (Tp), half‐time of crystallization (t1/2) 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 (Ea) calculated with the Kissinger model is higher when a small amount of MWNTs is added, then gradually decreases; all the Ea 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. Copyright © 2008 Society of Chemical Industry

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Tài liệu tham khảo

10.1038/354056a0

10.1038/363603a0

10.1142/p080

10.1126/science.265.5176.1212

10.1002/(SICI)1521-4095(200005)12:10<750::AID-ADMA750>3.0.CO;2-6

10.1038/423703a

10.1002/(SICI)1521-4095(199910)11:15<1281::AID-ADMA1281>3.0.CO;2-6

10.1063/1.1651339

10.1021/jp027726x

10.1021/nl034028v

10.1021/ma021263b

10.1016/S0009-2614(00)01013-7

10.1016/S0921-5093(99)00263-4

10.1016/S0025-5408(01)00775-9

10.1016/S0032-3861(02)00151-9

10.1016/j.polymer.2006.06.027

10.1088/0957-4484/17/10/005

10.1088/0957-4484/18/14/145606

10.1002/pi.2212

10.1021/jp014622y

10.1002/app.20703

10.1002/mame.200300303

10.1021/nl034336t

10.1016/j.polymer.2004.04.031

10.1021/ma049132t

10.1016/j.eurpolymj.2006.08.018

10.1021/ma049768k

10.1016/S0032-3861(03)00344-6

10.1002/polb.10028

10.1016/j.polymer.2004.04.057

10.1016/S0032-3861(97)10132-X

Lanza RP, 1998, Principles of Tissue Engineering

10.1002/mame.200500003

10.1002/(SICI)1521-3927(20000201)21:3<117::AID-MARC117>3.0.CO;2-X

10.1021/cm960514q

Pitt CG, 1980, Controlled Release of Bioactive Materials, 186

10.1002/pen.20620

10.1002/polb.20722

10.1016/j.polymdegradstab.2007.02.019

10.1016/j.polymer.2005.05.101

10.1295/polymj.26.786

10.1016/0032-3861(71)90041-3

10.1002/pen.11700

10.1103/PhysRevLett.84.1820

10.1063/1.1487900

10.1016/0032-3861(78)90060-5

10.1039/tf9454100365

10.1002/polb.20740

10.1016/S0032-3861(96)00552-6

10.1016/j.polymer.2003.10.028

10.1016/0022-3093(93)90736-H

10.1016/0022-3093(93)90737-I

10.1016/S0014-3057(96)00159-0

10.1007/BF03219011

10.6028/jres.057.026

10.1002/1521-3927(20020901)23:13<771::AID-MARC771>3.0.CO;2-G

10.1016/S0040-6031(00)00443-3

Flynn JH, 1966, J Res Natl Bur Stand (US), 487, 70A

10.1246/bcsj.38.1881

10.1021/jp026592k

10.1002/polc.5070060121

10.1002/1096-987X(20010130)22:2<178::AID-JCC5>3.0.CO;2-#

10.1016/S0040-6031(03)00258-2

10.1016/S0142-9418(03)00078-3

10.1016/j.tca.2004.09.001

10.1016/0032-3861(95)90934-T

10.1021/nl035009o

10.1016/j.polymer.2006.03.076

10.1002/app.1994.070510705

10.1002/polb.20527

10.1016/j.polymer.2005.06.094

10.1023/A:1026362727368