聚苯乙烯
结晶度
傅里叶变换红外光谱
辐照
离子
聚合物
材料科学
分析化学(期刊)
通量
光化学
红外光谱学
红外线的
化学
化学工程
结晶学
有机化学
光学
工程类
物理
核物理学
作者
Shiv Govind Prasad,Chhagan Lal
标识
DOI:10.1016/j.radphyschem.2023.111300
摘要
The effects of 1.75 MeV N5+ ion beams of varying fluences, ranging from 1 × 1011 to 1 × 1014 ions/cm2, have been used to investigate the structural, optical, and chemical properties of polystyrene using X-ray diffraction (XRD), UV–Visible spectroscopic, and Fourier transform infrared (FTIR) spectroscopic techniques. The changes in polystyrene polymer depend on ion fluence. The crystallinity has been increased drastically up to the ion fluence of 5 × 1012 ions/cm2, and decreases further up to 1 × 1014 ions/cm2. The energy of the direct bandgap is found to be reduced by up to 50% when compared to the pristine one. The shift in absorption maxima towards a higher wavelength supports color development in polymer films and is due to the formation of extended conjugation. The developments of FTIR peaks at 1601, 1697, 3321, and 3723 cm−1 support the existence of aromatic rings, carbonyl (>CO), acetylenic (-CC-), and hydroxyl functional groups in the irradiated polystyrene. Functional group generation is exponentially dependent on the quantity of ion fluences. The reaction mechanism of degradation products formation chemistry has been discussed.
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