Time-resolved LIBS of atomic and molecular carbon from coal in air, argon and helium

被引:102
作者
Dong, Meirong [1 ,2 ]
Mao, Xianglei [1 ]
Gonzalez, Jhanis J. [1 ]
Lu, Jidong [2 ]
Russo, Richard E. [1 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA
[2] S China Univ Technol, Sch Elect Power, Guangzhou 510640, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
INDUCED BREAKDOWN SPECTROSCOPY; LASER-ABLATION; TEMPERATURE-MEASUREMENTS; ELEMENTAL ANALYSIS; PLASMA PLUME; GRAPHITE; EMISSION; NITROGEN; SPECTRA; C-2;
D O I
10.1039/c2ja30222e
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Laser ablation chemical analysis of a coal sample was studied by LIBS (laser-induced breakdown spectroscopy). Ablation was performed using a 266 nm Nd:YAG laser in different gas environments (air, argon and helium) at atmospheric pressure. We present characteristics of spectra measured from coal with special attention to atomic and molecular carbon including CI, C-2 and CN. The influence of the ambient gas on the laser-induced coal plasma was studied by using time-resolved analysis. Atomic iron emission lines were employed to construct Boltzmann plots for the plasma excitation temperature. Computer simulations of C-2 spectra were used to deduce the molecular rotational temperature. Electron density and total atomic and molecular number density are reported to describe emission differences of atomic and molecular carbon in the different gas environments. These data demonstrate that the plasma excitation temperature is the primary factor contributing to differences among the atomic carbon emission in the gas environments. Reactions between the plasma species and ambient gas, and the total molecular number are main factors influencing molecular carbon emission. Finally, the influence of laser energy on the rotational temperature was studied in the air environment to demonstrate that the rotational temperature derived from C-2 band emission can be utilized to correct plasma fluctuations.
引用
收藏
页码:2066 / 2075
页数:10
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