scholarly journals The 12th Asilomar conference of mass spectrometry, September 20 – 24, 1996 “elemental mass spectrometry,” Gary M. Hieftje, program chair The Asilomar conference center, Pacific Grove, California

1996 ◽  
Vol 7 (9) ◽  
pp. 990-990
2011 ◽  
Vol 83 (7) ◽  
pp. 2425-2429 ◽  
Author(s):  
R. Kenneth Marcus ◽  
C. Derrick Quarles ◽  
Charles J. Barinaga ◽  
Anthony J. Carado ◽  
David W. Koppenaal

2019 ◽  
Vol 91 (6) ◽  
pp. 3773-3777 ◽  
Author(s):  
Joseph E. Lesniewski ◽  
Kunyu Zheng ◽  
Paolo Lecchi ◽  
David Dain ◽  
Kaveh Jorabchi

2019 ◽  
Vol 34 (3) ◽  
pp. 426-459 ◽  
Author(s):  
Andrew Taylor ◽  
Nicola Barlow ◽  
Martin P. Day ◽  
Sarah Hill ◽  
Nicholas Martin ◽  
...  

This review discusses developments in elemental mass spectrometry, atomic absorption, emission and fluorescence, XRF and LIBS, as applied to the analysis of specimens of clinical interest, foods and beverages. Sample preparation procedures and quality assurance are also included.


1992 ◽  
Vol 46 (3) ◽  
pp. 401-406 ◽  
Author(s):  
George R. Agnes ◽  
Gary Horlick

Preliminary results for the analytical use of electrospray mass spectrometry (ES-MS) for elemental analysis are presented. Spectra with the declustered plus-one ion (M+) as the dominant species have been measured for the alkali metals (Li, Na, K, Rb, and Cs) and for several transition metals (Cr, Mn, Fe, Co, Ni, Cu, Zn, Ag, and Cd) in both aqueous and methanol solvents. A number of background ions are also observed including MH+, MO+, MOH+, and MOH(H2O)+. For vanadyl sulfate and uranyl nitrate, ES conditions can be adjusted to produce VO+ and UO2+ as the dominant ions in the mass spectra, indicating that direct speciation of inorganic solution components is possible. On the basis of these preliminary results, it appears that electrospray may offer a low-cost and simple generic ion source for elemental mass spectrometry.


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