Abstract

The first of two new methods for reducing oxide interferences in inductively coupled plasma mass spectrometry is described. This method utilizes careful manipulation of the central-channel gas flow to impart distinguishable frequency-specific behavior to analyte and oxide species. Subsequently, application of a Fourier transform (FT) permits contributions from the analyte and oxide superimposed at a given mass to be unraveled. Through application of this correction method, a greater than ten-fold error at m/z 156 caused by the interference of 140Ce16O+ on 156Gd+ has been effectively eliminated. This correction method is well suited for overcoming multiple analyte–oxide interferences (most notably where monoisotopic elements have been compromised) in a simultaneous manner. Although a time-of-flight mass analyzer was utilized here, this correction method is well suited also for implementation with scan-based systems (e.g. quadrupoles and sector-field mass spectrometers).

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