Non-Isothermal Crystallization Behaviors of Poly (Trimethylene Terephthalate Isophthalate-Co-Polyethylene Glycol) with Lower Melting Point

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The non-isothermal crystallization behaviors of poly (trimethylene terephthalate) (PTT), poly (trimethylene terephthalate-co-isophthalate) (PTTI) and poly (trimethylene terephthalate isophthalate-co-polyethylene glycol) (PTTI-PEG) were investigated using Differential Scanning Calorimetry (DSC). The experimental results showed the crystallization temperature of PTT, PTTI and PTTI-PEG increased when the heating rate increased, and the Avrami exponents n of PTT, PTTI ranged from 3.5 to 5.5, and it was assumed that the non-isothermal crystallization mechanism for PTT and PTTI was the combination of homogenous and heterogeneous nucleation. However, the n value of PTTI-PEG was below 2.5, and the non-isothermal crystallization mechanism was ascribed to heterogeneous nucleation different from that of PTT and PTTI. The activation energy of PTTI increased with the IPA ratios increasing, and the activation energy of PTTI-PEG was the highest, suggesting that the crystallization rate was more sensitive to the temperature in comparison with PTT. Therefore, it was of great importance to control the temperature in processing.

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Advanced Materials Research (Volumes 332-334)

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275-280

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September 2011

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© 2011 Trans Tech Publications Ltd. All Rights Reserved

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[1] I. Aravind, K.J. Eichhorn, H. Komber, D. Jehnichen and S. Thomas: J. Phys. Chem. B, Vol. 113 (2009),p.1569

Google Scholar

[2] R.M. Ho: Macromolecules, Vol. 33 (2000),p.7529

Google Scholar

[3] T. Wu, Y. Li, Q. Wu, L. Song and G. Wu: Europ. Poly. J., Vol. 41 (2005),p.2216

Google Scholar

[4] K.Q. Chen, X.Z. Tang, J. Shen, Y. Zhou and B. Zhang: Macromol. Mater. Eng. Vol. 289 (2004),p.539

Google Scholar

[5] S. Kalakkunnath and D.S. Kalika: Polymer, Vol. 47 (2006),p.7085

Google Scholar

[6] H.H. Chuah: Macromolecules, Vol. 34 (2001),p.6985

Google Scholar

[7] T.W. Shyr, C.M. Lo and S.R. Ye: Eur. Polymer, Vol.46 (2005),p.5284

Google Scholar

[8] H.B. Jia, Y. Xu, S.R. Ye and J.W. Qian: J. Mater. Sci., Vol. 41 (2007),p.8381

Google Scholar

[9] Y. Xu, H.B. Jia, S.R. Ye and J. Huang: J. Mater. Sci., Vol. 42 (2006),p.31

Google Scholar

[10] C.Y. Ko, M. Chen, C.L. Wang, H.C. Wang, R.Y. Chen and I.M. Tseng: Polymer, Vol. 48 (2007),p.2415

Google Scholar

[11] Y.Y. Yao, L.C. Cui, C.M. Jiang, W.Y. Lv, X.H. Wang, Z.C. Huang and W.X Chen: Journal of Textile Research, Vol. 32 (2011),p.1

Google Scholar

[12] M. Avrami: J. Chem. Phys., Vol. 12 (1939),p.1103

Google Scholar

[13] M. Avrami: J. Chem. Phys., Vol. 8(1940),p.212

Google Scholar

[14] M. Avrami: J. Chem. Phys., Vol. 9(1941),p.177

Google Scholar

[15] L. Mandelkern: Methods of Experimental Physics (Academic Press, New York 1980)

Google Scholar

[16] A. Jeziorny: Polymer, Vol. 10 (1978),p.1142

Google Scholar

[17] H. E. Kissinger: Anal. Chem., Vol. 29(1957),p.1702

Google Scholar