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Resonance ionization mass spectrometry of uranium with intracavity laser ionization

Journal Article · · Anal. Chem.; (United States)
DOI:https://doi.org/10.1021/ac00268a058· OSTI ID:5234355
Resonance ionization mass spectrometry (RIMS) is a highly selective and sensitive tool for elemental and isotopic analysis. While most RIMS work to date has been carried out with high-power pulsed lasers, it has been suggested and verified, that continuous wave (CS) lasers may prove to be a viable alternative. One expects that increases in laser intensity should lead to increased ion yields for CW excitation. For CW, and in some cases flashlamp-pumped dye lasers, it is well-known that the circulating power inside the cavity is much greater than that coupled out of the cavity. The cavity of a flashlamp-pumped dye laser was extended to contain the source region of a time-of-flight mass spectrometer. Experiments were carried out with uranium, using the three-photon doubly resonant ionization at 591.5 nm. This process is particularly attractive for uranium because photons of a single nominal frequency are resonant with both bound-bound transitions. Thus, a single laser can be used to ionize uranium through sequential resonances. 22 references, 2 figures.
Research Organization:
Los Alamos National Lab., NM
OSTI ID:
5234355
Journal Information:
Anal. Chem.; (United States), Journal Name: Anal. Chem.; (United States) Vol. 56:4; ISSN ANCHA
Country of Publication:
United States
Language:
English