碳化
衣康酸
聚丙烯腈
丙烯腈
聚合
材料科学
碳纤维
傅里叶变换红外光谱
脱氢
高分子化学
催化作用
化学
有机化学
化学工程
聚合物
吸附
复合材料
共聚物
工程类
复合数
作者
Ravindra V. Ghorpade,Sungho Lee,Sung Chul Hong
标识
DOI:10.1016/j.polymdegradstab.2020.109373
摘要
The carbonization procedure is a crucial step for polyacrylonitrile (PAN)-based precursors to be transformed into carbon materials. In this study, PAN and poly(acrylonitrile-co-itaconic acid)s (PAIs) with different contents of itaconic acid (IA) were prepared through free radical polymerization, and their carbonization behaviors were investigated at different thermal treatment temperatures. As confirmed by Fourier transform infrared spectroscopy analyses, functional groups containing heteroatoms practically disappeared above 600 °C, due to crosslinking, condensation, dehydrogenation, and gas-evolution reactions of the carbonization processes. Deconvolution of the carbon, oxygen and nitrogen peaks from X-ray photoelectron spectroscopy analyses revealed the development of ordered and doped graphitic carbons at elevated thermal treatment temperatures. The total yields of PAIs with excess amounts of IA (3 ~ 6 mol%) demonstrated a large carbon loss during the carbonization procedures. PAI with 1 ~ 2 mol% IA afforded carbon materials with a relatively high graphitic carbon content at 1200 °C, which is potentially important for electrical conductivity. Meanwhile, carbon materials prepared from PAI with 2 mol% IA at 1200 °C exhibited a relatively high content of pyridinic nitrogen, suggesting potentially superior catalytic activity. This study afforded technical guidelines on the structural elements of PAN-based precursors to prepare carbon materials with predesigned characteristics.
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