journal article·2021-07Open access

Structure, stability, and properties of phenolic fibers modified by phenyl molybdate

Yang Kai, Jiao Mingli, Zhang Xiaomei, Jia Wanshun, Diao Quan, Liu Ying, Cao Jian

Polymers and Polymer Composites· Volume 29· Issue 6

Abstract

Phenyl molybdate-modified phenolic fibers (PMoPFs) were prepared by melt spinning from the corresponding resin which was polymerized from phenol, formaldehyde, and phenyl molybdate, followed by solution curing and then heat curing processes. The molecular structures, including characteristic groups and molecular weight, were examined by nuclear magnetic resonance, Fourier transform infrared spectroscopy, and gel permeation chromatography. The influences of the curing processes were demonstrated by mechanical properties, scanning electron microscopy, and thermogravimetric analysis characterization. PMoPF with 8 wt% molybdic acid and cured in an oven possessed a tensile strength as high as 187 MPa, initial decomposition temperature of 300°C, and a char yield under nitrogen atmosphere at 800°C as high as 66.0%, with the molybdate (MoO 4 2− ) groups being introduced into the phenolic main chain.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Flame retardant materials and properties · Synthesis and properties of polymers · Fiber-reinforced polymer composites

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Fashion Design and Engineering, School of Fashion, Zhongyuan University of Technology, Zhengzhou, China

Department of Polymer Materials and Engineering, School of Materials and Chemical Engineering, Zhongyuan University of Technology, Zhengzhou, China

Funding

the Science and Technology Foundation of Henan Province

References (26)

Show source-provided references
1. Economy J, Clark RA. Fibers from novolacs. Patent 3650102, USA, 1972.
2. 10.1016/0008-6223(94)90075-210.1016/0008-6223(94)90075-2 ↗
3. 10.1016/S0254-0584(01)00358-310.1016/S0254-0584(01)00358-3 ↗
4. 10.1016/j.matchemphys.2013.09.02710.1016/j.matchemphys.2013.09.027 ↗
5. 10.1007/s12221-012-0495-z10.1007/s12221-012-0495-z ↗
6. 10.1016/j.polymdegradstab.2005.05.02510.1016/j.polymdegradstab.2005.05.025 ↗
7. 10.2298/TSCI1504411J10.2298/TSCI1504411J ↗
8. 10.1016/j.polymer.2003.09.01910.1016/j.polymer.2003.09.019 ↗
9. 10.1080/10402004.2015.107740410.1080/10402004.2015.1077404 ↗
10. 10.1016/j.polymdegradstab.2003.09.01210.1016/j.polymdegradstab.2003.09.012 ↗
11. 10.1016/j.apsusc.2013.07.09710.1016/j.apsusc.2013.07.097 ↗
12. Liu X · Gongcheng Suliao Yingyong · 2002 · 30 · 4
13. 10.1021/ma60070a04610.1021/ma60070a046 ↗
14. 10.1002/app.2180810.1002/app.21808 ↗
15. 10.1016/j.poly.2015.09.00910.1016/j.poly.2015.09.009 ↗
16. 10.1007/s12221-016-5651-410.1007/s12221-016-5651-4 ↗
17. 10.1016/S0141-3910(03)00225-810.1016/S0141-3910(03)00225-8 ↗
18. Ouyang Z · Chem Ind Eng Prog · 2005 · 24 · 901
19. Qiang M · Naihuo Cailiao · 2005 · 39 · 119
20. 10.1016/j.mseb.2005.07.00510.1016/j.mseb.2005.07.005 ↗
21. 10.1016/j.apsusc.2005.08.06410.1016/j.apsusc.2005.08.064 ↗
22. 10.1016/j.matchemphys.2009.12.04210.1016/j.matchemphys.2009.12.042 ↗
23. 10.1080/10402004.2015.106502510.1080/10402004.2015.1065025 ↗
24. 10.1016/j.polymdegradstab.2007.11.00310.1016/j.polymdegradstab.2007.11.003 ↗
25. 10.1016/S0141-3910(02)00107-610.1016/S0141-3910(02)00107-6 ↗
26. 10.1016/S0141-3910(96)00171-110.1016/S0141-3910(96)00171-1 ↗