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Study on structures and properties of ultra-hot drawing UHMWPE fibers fabricated via dry spinning method

  • Xinwei Wang EMAIL logo , Han Zheng and Yongfei Sun
Published/Copyright: April 19, 2018
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Abstract

High tensile strength ultra high molecular weight polyethylene (UHMWPE) fibers were prepared via the dry spinning method. Raw material was UHMWPE resin with 6 million viscosity-average molecular weight (Mv). Changes of morphology, mechanical properties, thermal properties and crystallization process of the fibers in the ultra-hot drawing process were studied by scanning electron microscopy (SEM), tensile tester, differential scanning calorimetry (DSC), and wide-angle X-ray diffraction (WAXD). Results show that there was a maximum value of fracture force at a draw ratio of 40 and excessive draw ratio destroyed crystal structures in fibers and led to a decrease in the fracture force value. A shoulder peak appeared in DSC curves of ultra-drawing samples and its peak value maintained at 154°C in different samples. In addition, three peaks can be observed in all WAXD patterns of drawing samples. The mechanism of microstructural changes during the hot drawing process was elucidated.

  1. Funding: Science and Technonlogy Commission of shanghai Municipality, Grant Number: 16160731300.

References

[1] Barham PJ, Keller A. J. Mater. Sci. 1985, 20, 2281–2302.10.1007/BF00556059Search in Google Scholar

[2] Smith P, Lemstra PJ. J. Polym. Sci. Pol. Phys. 1979, 180, 2983–2986.10.1002/macp.1979.021801220Search in Google Scholar

[3] Smith P, Lemstra PJ, Kalb B, Pennings AJ. Polym. Bull. 1979, 1, 733–736.10.1007/BF00254487Search in Google Scholar

[4] Savitsky AV, Gorshkova IA, Frolova IL, Shmikk GN, Ioffe AF. Polym. Bull. 1984, 12, 195–202.10.1007/BF00275968Search in Google Scholar

[5] Murase H, Ohta Y, Hashimoto T. J. Polym. Sci. Pol. Chem. 2011, 44, 7335–7350.10.1021/ma2008817Search in Google Scholar

[6] Smith P, Lemstra PJ. Colloid Polym. Sci. 1980, 258, 891–894.10.1007/BF01566246Search in Google Scholar

[7] Bastiaansen CWM, Froehling P, Pijpers AJ, Lemstra PJ, Integration of Fundamental Polymer Science and Technology, Springer Netherlands: Netherlands, 1986.Search in Google Scholar

[8] Xiao M, Yu J, Zhu J, Chen L, Zhu J, Hu Z. J. Mater. Sci. 2011, 46, 5690–5697.10.1007/s10853-011-5520-xSearch in Google Scholar

[9] Smook J, Pennings J. Colloid Polym. Sci. 1984, 262, 712–722.10.1007/BF01451543Search in Google Scholar

[10] Liu H, Lv F, Li J, Cao T, Wan C, Zhang W, Li L, Zheng G, Shen C. J. Appl. Polym. Sci. 2015, 132, 42823.10.1002/app.42823Search in Google Scholar

[11] Karacan I. J. Appl. Polym. Sci. 2006, 101, 1317–1333.10.1002/app.22952Search in Google Scholar

[12] Yeh JT, Lin SC, Tu CW, Hsie KH, Chang FC. J. Mater. Sci. 2008, 43, 4892–4900.10.1007/s10853-008-2711-1Search in Google Scholar

[13] Hofmann D, Schulz E. Polymer 1989, 30, 1964–1968.10.1016/0032-3861(89)90279-6Search in Google Scholar

[14] Riekel C, Cedola A, Heidelbach F, Wagner K. Macromolecules 1997, 30, 1033–1037.10.1021/ma960799sSearch in Google Scholar

[15] Kwon YK, Boller A, Pyda M, Wunderlich B. Polymer 2000, 41, 6237–6249.10.1016/S0032-3861(99)00839-3Search in Google Scholar

[16] Hsieh YL, Hu XP. J. Polym. Sci. Pol. Phys. 1997, 35, 623–630.10.1002/(SICI)1099-0488(199703)35:4<623::AID-POLB10>3.0.CO;2-ISearch in Google Scholar

[17] Smook, J, Pennings. J. Colloid Polym. Sci. 1984, 262, 712–722.10.1007/BF01451543Search in Google Scholar

[18] Ratner S, Weinberg A, Marom G. Polym. Compos. 2003, 24, 422–427.10.1002/pc.10040Search in Google Scholar

[19] Hsieh YL, Ju J. J. Appl. Polym. Sci. 1994, 53, 347–354.10.1002/app.1994.070530312Search in Google Scholar

Received: 2017-11-25
Accepted: 2018-03-09
Published Online: 2018-04-19
Published in Print: 2018-10-25

©2018 Walter de Gruyter GmbH, Berlin/Boston

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