石墨
拉曼光谱
富勒烯
聚乙烯
材料科学
碳纤维
化学工程
纳米技术
物理
复合材料
化学
有机化学
复合数
光学
工程类
作者
Vilas G. Pol,Jianguo Wen,Kah Chun Lau,Samantha K. Callear,Daniel T. Bowron,C.-T Lin,Sanket A. Deshmukh,Subramanian K. R. S. Sankaranarayanan,Larry A. Curtiss,William I. F. David,Dean J. Miller,Michael M. Thackeray
出处
期刊:Carbon
[Elsevier]
日期:2014-03-01
卷期号:68: 104-111
被引量:43
标识
DOI:10.1016/j.carbon.2013.10.059
摘要
Monodispersed hard carbon spheres can be synthesized quickly and reproducibly by autogenic reactions of hydrocarbon precursors, notably polyethylene (including plastic waste), at high temperature and pressure. The carbon microparticles formed by this reaction have a unique spherical architecture, with a dominant internal nanometer layered motif, and they exhibit diamond-like hardness and electrochemical properties similar to graphite. In the present study, in situ monitoring by X-ray diffraction along with electron microscopy, Raman spectroscopy, neutron pair-distribution function analysis, and computational modeling has been used to elucidate the morphology and evolution of the carbon spheres that form from the autogenic reaction of polyethylene at high temperature and pressure. A mechanism is proposed on how polyethylene evolves from a linear chain-based material to a layered carbon motif. Heating the spheres to 2400–2800 °C under inert conditions increases their graphitic character, particularly at the surface, which enhances their electrochemical and tribological properties.
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