Synthesis, Characterization, and Cure Chemistry of Renewable Bis(cyanate) Esters Derived from 2-Methoxy-4-Methylphenol

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• 作者：Heather A. Meylemans ; Benjamin G. Harvey ; Josiah T. Reams ; Andrew J. Guenthner ; Lee R. Cambrea ; Thomas J. Groshens ; Lawrence C. Baldwin ; Michael D. Garrison ; Joseph M. Mabry
• 刊名：Biomacromolecules
• 出版年：2013
• 出版时间：March 11, 2013
• 年：2013
• 卷：14
• 期：3
• 页码：771-780
• 全文大小：470K
• 年卷期：v.14,no.3(March 11, 2013)
• ISSN：1526-4602

文摘

A series of renewable bis(cyanate) esters have been prepared from bisphenols synthesized by condensation of 2-methoxy-4-methylphenol (creosol) with formaldehyde, acetaldehyde, and propionaldehyde. The cyanate esters have been fully characterized by infrared spectroscopy, ¹H and ¹³C NMR spectroscopy, and single crystal X-ray diffraction. These compounds melt from 88 to 143 掳C, while cured resins have glass transition temperatures from 219 to 248 掳C, water uptake (96 h, 85 掳C immersion) in the range of 2.05鈥?.21%, and wet glass transition temperatures from 174 to 193 掳C. These properties suggest that creosol-derived cyanate esters may be useful for a wide variety of military and commercial applications. The cure chemistry of the cyanate esters has been studied with FTIR spectroscopy and differential scanning calorimetry. The results show that cyanate esters with more sterically demanding bridging groups cure more slowly, but also more completely than those with a bridging methylene group. In addition to the structural differences, the purity of the cyanate esters has a significant effect on both the cure chemistry and final T_g of the materials. In some cases, post-cure of the resins at 350 掳C resulted in significant decomposition and off-gassing, but cure protocols that terminated at 250鈥?00 掳C generated void-free resin pucks without degradation. Thermogravimetric analysis revealed that cured resins were stable up to 400 掳C and then rapidly degraded. TGA/FTIR and mass spectrometry results showed that the resins decomposed to phenols, isocyanic acid, and secondary decomposition products, including CO₂. Char yields of cured resins under N₂ ranged from 27 to 35%, while char yields in air ranged from 8 to 11%. These data suggest that resins of this type may potentially be recycled to parent phenols, creosol, and other alkylated creosols by pyrolysis in the presence of excess water vapor. The ability to synthesize these high temperature resins from a phenol (creosol) that can be derived from lignin, coupled with the potential to recycle the composites, provides a possible route to the production of sustainable, high-performance, thermosetting resins with reduced environmental impact.