Hyperfine structures and isotopic shifts of uranium transitions using tunable laser spectroscopy of laser ablation plumes

被引:33
|
作者
Harilal, S. S. [1 ]
Murzyn, C. M. [2 ]
Phillips, M. C. [3 ,4 ]
Martin, J. B. [2 ]
机构
[1] Pacific Northwest Natl Lab, Richland, WA 99352 USA
[2] Sandia Natl Labs, POB 5800, Albuquerque, NM 87185 USA
[3] Univ Arizona, Coll Opt Sci, Tucson, AZ 85721 USA
[4] Opticslah LLC, Albuquerque, NM 87106 USA
关键词
Laser ablation; Laser-induced fluorescence; Laser absorption spectroscopy; LIBS; Tunable laser spectroscopy; Isotopic analysis; Hyperfine structure; Uranium; INDUCED BREAKDOWN SPECTROSCOPY; FLUORESCENCE SPECTROSCOPY; ABSORPTION-SPECTROSCOPY; SOLID SAMPLES; U-235; EMISSION; SOIL;
D O I
10.1016/j.sab.2020.105828
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
We report isotopic shifts and hyperfine structures of selected U transitions employing tunable spectroscopy viz: laser-induced fluorescence and laser absorption spectroscopy of laser ablation plumes. The plasmas were produced during ns laser ablation on a natural U metal target which contains 0.73% U-235. Our results show that isotopic shifts between U-238 and U-235 are entangled with hyperfine structures of U-235. Measurements obtained using laser-induced fluorescence are affected by the high absorbance of U-238. Time-resolved laser absorption spectroscopy is carried out for evaluating the optical absorption and estimating the hyperfine constants.
引用
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页数:8
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