Chem. J. Chinese Universities ›› 2019, Vol. 40 ›› Issue (5): 1071.doi: 10.7503/cjcu20180751

• Polymer Chemistry • Previous Articles     Next Articles

Synthesis and Properties of a Novel Bio-based Benzoxazine

YIN Ping1,2, YAN Hongqiang1,*(), CHENG Jie1, FANG Zhengping1   

  1. 1. Laboratory of Polymer Material and Engineering, Ningbo Institute of Technology, Zhejiang University, Ningbo 315100, China
    2. Chemical Engineering and Bioengineering, Zhejiang University, Hangzhou 310027, China
  • Received:2018-11-06 Online:2019-03-29 Published:2019-03-29
  • Contact: YAN Hongqiang E-mail:yanhongqiang@nit.net.cn
  • Supported by:
    † Supported by the Natural Science Foundation of Zhejiang Province, China(No.LY19E030004), the Natural Science Foundation of Ningbo City, China(No.2018A610184) and the Major Industrial Projects of Ningbo City, China(No.2015B11005)

Abstract:

A novel bio-based benzoxazine resin(phenolphthalein-furfuramine-benzoxazine, PTL-F-BOZ), used bio-based furfurylamine, phenolphthalein, and paraformaldehyde as raw materials, was synthesized and characterized by Fourier transform infrared spectroscopy(FTIR), nuclear magnetic resonance(1H NMR and 13C NMR). The curing, thermal and flame retardant properties were analyzed by differential scanning calorimetric(DSC), thermogravimetric analyzer(TG), limiting oxygen index(LOI), vertical burning test, microscale combustion calorimetry(MCC), cone calorimeter(Cone) and scanning electron microscope(SEM). The DSC curve of PTL-F-BOZ showed a two-stage curing with two maxima at 224 and 251 ℃ respectively, and had lower curing temperature than that of the traditional fossil-based bisphenol benzoxazine bisphenol A-aniline benzoxazine(bisphenol A-aniline-benzoxazine, BPA-A-BOZ). The presence of the furan ring in the furfurylamine increased the cross-linking density of polymer, retarded the rearrangement reaction from the phenoxy structure to the phenol structure, and resulted in two curing peaks in the DSC curve of PTL-F-BOZ. Under nitrogen and air atmospheres, the temperatures of 5% mass loss(T5%) for PPTL-F-BOZ resin were 380 and 370 ℃, respectively and the residual chars at 800 ℃ were 63.0% and 10.5%, respectively. Compared with PBPA-A-BOZ resin, PPTL-F-BOZ resin both possessed higher T5% and residual char of 800 ℃. From the DTG curve, the maximum mass loss rates of two decomposition stage(Peak 1 and Peak 2 values) of PPTL-F-BOZ resin were 0.67%/min and 3.28%/min, which were only 7.38% and 63.44% of PBPA-A-BOZ(9.07%/min and 5.17%/min) under nitrogen atmosphere, and those were also the same under air atmosphere. LOI of PPTL-F-BOZ resin was 36.2%, which was higher than that of PBPA-A-BOZ resin. Meanwhile, in the UL-94 test, PPTL-F-BOZ resin extinguished quickly and released less smoke during combustion process, and the original morphology was kept well and a stable carbon layer was formed after burning. Its first ignition time(t1) and second ignition time(t2) were 1.4 and 8.5 s, respectively, far smaller than the maximum permissible values of 10 s, and a UL94 V-0 rating was also achieved. Hence, PPTL-F-BOZ resin showed excellent thermal and flame retardant properties.

Key words: Bio-based benzoxazine, Phenolphthalein-furfuramine-benzoxazine resin, Curing reaction, Thermal property, Flame retardancy

CLC Number: 

TrendMD: