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Determination of boron with molecular emission using laser-induced breakdown spectroscopy combined with laser-induced radical fluorescence
被引:41
|作者:
Guo, L. B.
[1
]
Zhu, Z. H.
[1
]
Li, J. M.
[1
]
Tang, Y.
[1
]
Tang, S. S.
[1
]
Hao, Z. Q.
[1
,2
]
Li, X. Y.
[1
]
Lu, Y. F.
[1
]
Zeng, X. Y.
[1
]
机构:
[1] Huazhong Univ Sci & Technol, WNLO, Wuhan 430074, Hubei, Peoples R China
[2] Yichun Univ, Coll Phys Sci & Engn Technol, Yichun 336000, Jiangxi, Peoples R China
来源:
基金:
中国博士后科学基金;
中国国家自然科学基金;
关键词:
SPECTROMETRY;
LIBS;
QUANTIFICATION;
PRESSURE;
ABLATION;
BANDS;
STEEL;
D O I:
10.1364/OE.26.002634
中图分类号:
O43 [光学];
学科分类号:
070207 ;
0803 ;
摘要:
Boron is an essential element for industry, but it is hard to accurately and rapidly determine high boron content with conventional laser-induced breakdown spectroscopy (LIBS), due to the matrix and self-absorption effect. Using molecular emission is an alternative method for boron content analysis, but its weak spectra are major challenges. Here, boron monoxide (BO) radicals were used to establish calibration assisted by LIBS and laser-induced radical fluorescence (LIBS-LIRF). Two types of BO radical excitations, vibrational ground state excitation (LIRFG) and vibrational excited state excitation (LIRFE), were compared. The results showed that LIRFG achieved better sensitivity with a limit of detection of 0.0993 wt.%, while the LIRFE was more accurate with a root mean square error of cross validation of 0.2514 wt.%. In conclusion, this work provided a potential approach for molecular emission analysis with LIBS-LIRF. (C) 2018 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
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页码:2634 / 2642
页数:9
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