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C-13-NMR study on cure-accelerated phenol-formaldehyde resins with carbonates

机译:碳酸盐固化促进的酚醛树脂的C-13-NMR研究

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摘要

Both liquid- and solid-state carbon-13-nuclear magnetic resonance (C-13-NMR) spectroscopies mere used to investigate the cure acceleration effects of three carbonates (propylene carbonate, sodium carbonate, and potassium carbonate) on liquid and cured phenol-formaldehyde (PF) resins. The liquid-phase C-13-NMR spectra showed that the cure acceleration mechanism in the propylene carbonate-added PF resin seemed to be involved in increasing reactivity of the phenol rings, whereas the addition of both sodium carbonate and potassium carbonate into PF resin apparently resulted in the presence of ortho-ortho methylene linkages. Proton spin-lattice rotating frame relaxation time (T-1 rho H) measured by solid-state C-13 cross polarization/magic-angle spinning NMR spectroscopy was smaller for the cure-accelerated PF resins than that of the control PF resin. The result indicated that the cure-accelerated PF resins are less rigid than the control PF resin. (C) 2000 John Wiley & Sons, Inc. [References: 34]
机译:液态和固态碳13核磁共振谱(C-13-NMR)均仅用于研究三种碳酸盐(碳酸亚丙酯,碳酸钠和碳酸钾)对液体和固化苯酚的固化促进作用。甲醛(PF)树脂。液相C-13-NMR谱表明,在添加碳酸亚丙酯的PF树脂中,固化促进机理似乎与酚环反应性的提高有关,而向PF树脂中同时加入碳酸钠和碳酸钾则明显导致存在邻-邻亚甲基键。对于固化促进的PF树脂,通过固态C-13交叉极化/魔角旋转NMR光谱法测量的质子自旋晶格旋转框架弛豫时间(T-1 rho H)小于对照PF树脂。结果表明,固化促进的PF树脂的硬度低于对照PF树脂。 (C)2000 John Wiley&Sons,Inc. [参考:34]

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