Non-isothermal crystallization of HDPE/nano-SiO2 composite
Source abstract
Abstract
The kinetics of non-isothermal crystallization of high density polyethylene/nano-scale silicon dioxide (HDPE/nano-SiO2) composite was investigated by means of differential scanning calorimetry at various cooling rates. Several theoretical models were applied to describe the process of non-isothermal crystallization. The results showed that the Avrami analysis modified by Jeziorny or by Mo's treatment could describe the non-isothermal crystallization of the composite very well, but the Ozawa analysis did not give an adequate description. The Avrami exponent n of HDPE/nano-SiO2 composite is slightly larger than that of HDPE. The values of half-time t 1/2 and Z c showed that the crystallization rate increased with increasing cooling rates for both HDPE and HDPE/nano-SiO2 composite, but the crystallization rate of HDPE/nano-SiO2 composite was faster than that of HDPE. The activation energies were estimated to be 166.3, 206.2, 251.1 and 266.0 kJ/mol for non-isothermal crystallization of pure HDPE and HDPE/nano-SiO2 composites with different SiO2 loadings of 1%, 3%, and 5% respectively.
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Research context
OpenAlex topics: Polymer crystallization and properties · Polymer Nanocomposites and Properties · biodegradable polymer synthesis and properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (20)
Show source-provided references
1. Z. H. Liu, K. W. Kwok, R. K. Li and C. L. Choy, Polymer 43 (2002) 2501.10.1016/S0032-3861(02)00048-4 ↗
2. W. Thongruang, C. M. Balik and R. J. Spontak, J. Polym. Sci. Part B: Polym. Phys. 40 (2002) 1013.10.1002/polb.10157 ↗
3. J. Suwanprateeb, J. Appl. Polym. Sci. 75 (2000) 1503.10.1002/(SICI)1097-4628(20000321)75:12<1503::AID-APP9>3.0.CO;2-X ↗
4. V. P. Privalko, D. I. Sukhorukov, E. G. Privalko, R. Walter, K. Friedrich and F. J. BaltÁ Calleja,ibid. 73 (1999) 1041.10.1002/(SICI)1097-4628(19990808)73:6<1041::AID-APP23>3.0.CO;2-6 ↗
5. H. G. Jeon, H. T. Jung, S. W. Lee and S. D. Hudson, Polymer Bulletin 41 (1998) 107.10.1007/s002890050339 ↗
6. T. Li, G. Liu and K. Qi, J. Appl. Polym. Sci. 67 (1998) 1227.10.1002/(SICI)1097-4628(19980214)67:7<1227::AID-APP10>3.0.CO;2-Z ↗
7. W. B. Xu, M. L. Ge and P. S. He, J. Polym. Sci. Part B: Polym. Phys. Ed. 40 (2002) 408.10.1002/polb.10101 ↗
8. Idem., J. Appl. Polym. Sci. 82 (2001) 2281.10.1002/app.2076 ↗
9. Q. A. Zheng, M. Peng and X. S. Yi, Materials Letters 40 (1999) 91.10.1016/S0167-577X(99)00054-3 ↗
10. W. P. Xu, R. Huang, B. H. Cai and W. Fan, China Plastics 12(6) (1998) 30 (in Chinese).
11. P. He and A. C. Zhao, Plastics 30(1) (2001) 39 (in Chinese).
12. M. L. Di lorenzo and C. Silvestre, Prog. Polym. Sci. 24 (1999) 917.10.1016/S0079-6700(99)00019-2 ↗
13. A. Jeziorny, Polymer 19 (1979) 1142.10.1016/0032-3861(78)90060-5 ↗
14. A. K. Gupta, S. K. Rana and B. L. Deopura, J. Appl. Polym. Sci. 51 (1994) 231.10.1002/app.1994.070510204 ↗
15. T. Ozawa, Polymer 12 (1971) 150.10.1016/0032-3861(71)90041-3 ↗
16. M. Eder and A. Wlochowicz, ibid. 24 (1983) 1593.10.1016/0032-3861(83)90177-5 ↗
17. T. Liu, Z. S. Mo, S. Wang and H. Zhang, Polym. Eng. Sci. 37 (1997) 568.10.1002/pen.11700 ↗
18. Y. An, L. Li, L. Do, Z. Mo and Z. Feng, J. Polym. Sci. Part B: Polym. Phys. 37 (1999) 443.10.1002/(SICI)1099-0488(19990301)37:5<443::AID-POLB4>3.0.CO;2-B ↗
19. H. E. Kissinger, J. Res. Natl. Stds. 57 (1956) 217.10.6028/jres.057.026 ↗
20. S. Jiang, D. Yu, X. Ji, L. An and B. Jiang, Polymer 41 (2000) 2041.10.1016/S0032-3861(99)00342-0 ↗