Studies on Crystal Transition of Polyamide 11 Nanocomposites by Variable-temperature X-Ray Diffraction

Tian-xi Liu; Dan Chen; In Yee Phang; Chun Wei

doi:10.1007/s10118-014-1383-3

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Studies on Crystal Transition of Polyamide 11 Nanocomposites by Variable-temperature X-Ray Diffraction

Note | Updated：2021-06-21

- Studies on Crystal Transition of Polyamide 11 Nanocomposites by Variable-temperature X-Ray Diffraction
- Chinese Journal of Polymer Science Vol. 32, Issue 1, Pages: 115-122(2014)
- Affiliations：
  
  a.Key Laboratory of New Processing Technology for Nonferrous Metals and Materials, Ministry of Education, College of Materials Science and Engineering, Guilin University of Technology, Guilin 541004, China
  b.State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science, Fudan University, Shanghai 200433, China
  c.Institute of Materials Research and Engineering, A*STAR (Agency for Science, Technology and Research), 3 Research Link, 117602, Singapore
- Author bio：
  
  **Tian-xi Liu (刘天西), E-mail: txliu@fudan.edu.cn
  Chun Wei (韦春), E-mail: 1986024@glut.edu.cn
- Funds：
- DOI：10.1007/s10118-014-1383-3
  CLC：
- Received：26 August 2013，
  
  Revised：2013-10-06，
  
  Accepted：09 October 2013，
  
  Published：2014-01
- Accepted：
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Tian-xi Liu, Dan Chen, In Yee Phang, et al. Studies on Crystal Transition of Polyamide 11 Nanocomposites by Variable-temperature X-Ray Diffraction[J]. Chinese Journal of Polymer Science, 2014, 32(1): 115-122.
DOI：

Tian-xi Liu, Dan Chen, In Yee Phang, et al. Studies on Crystal Transition of Polyamide 11 Nanocomposites by Variable-temperature X-Ray Diffraction[J]. Chinese Journal of Polymer Science, 2014, 32(1): 115-122. DOI： 10.1007/s10118-014-1383-3.

摘要

Abstract

Polyamide 11 (PA11) and its nanocomposites with different organoclay loadings were prepared by melt-compounding and subsequent pelletizing. The crystal phase transitions of PA11 and its clay nanocomposites were investigated by variable-temperature X-ray diffraction. It was found that the Brill transition of the nanocomposite was 20 K higher than that of the neat PA11 for both heating and cooling processes. The PA11

-spacings of the nanocomposites were observed to be smaller than those of the neat PA11 for melt crystallization. The constraints imposed by the addition of layered clay

restricting the thermal expansion of the polymer chains

are probably responsible for such a reduction of the

-spacing.

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