“…CO 2 (2,362 and 2,308 cm −1 ), phenol derivative (3,654 cm −1 for C aromatic -OH, 3,013 and 1,508 cm −1 for C aromatic -H, 1,604 cm −1 for C aromatic = C aromatic , and 1,174 cm −1 for C aromatic -O), methane (2,997 and 1,302 cm −1 ), carbonyl-containing compound (1,235 cm −1 for C carbonyl -O and 1,788 cm −1 for C=O), para-disubstituted benzene and unsubstituted benzene (824 and 668 cm −1 ) are the dominating products of pure PC within 40 wt% mass loss. [25,47] For PC-13.5% A3 (Figure 10b), the disappearance of the peaks at 3,013, 2,997, 824 -, and 668 cm −1 within 5% mass loss indicates that the decomposition process of PC is delayed. This phenomenon suggests the combustion of PC is effectively inhibited.…”