Reaction chemistry and collisional processes in multipole devices for resolving isobaric interferences in ICP-MS

• Published in: Analytical and bioanalytical chemistry 2001-07, Vol.370 (5), p.454-470
• Main Authors: BANDURA, D. R, BARANOV, V. I, TANNER, S. D
• Format: Article
• Language: English
• Subjects: Analytical chemistry; Chemical reactions; Chemistry; Damping; Dipole interactions; Exact sciences and technology; Fragmentation; Hydroxylation; Interference; Ions; Multipoles; Neutral gases; Oxidation; Spectrometric and optical methods; Zirconium
• ISSN: 0937-0633; 1618-2642; 1432-1130; 1618-2650
• DOI: 10.1007/s002160100869

A low-level review of the fundamentals of ion-molecule interactions is presented. These interactions are used to predict the efficiencies of collisional fragmentation, energy damping and reaction for a variety of neutral gases as a function of pressure in a rf-driven collision/reaction cell. It is shown that the number of collisions increases dramatically when the ion energies are reduced to near-thermal (< 0.1 eV), because of the ion–induced dipole and ion–dipole interaction. These considerations suggest that chemical reaction can be orders of magnitude more efficient at improving the analyte signal/background ratio than can collisional fragmentation. Considerations that lead to an appropriate selection of type of gas, operating pressure, and ion energies for efficient operation of the cell for the alleviation of spectral interferences are discussed. High efficiency (large differences between reaction efficiencies of the analyte and interference ions, and concomitant suppression of secondary chemistry) might be required to optimize the chemical resolution (determination of an analyte in the presence of an isobaric interference) when using ion-molecule chemistry to suppress the interfering ion. In many instances atom transfer to the analyte, which shifts the analytical m/z by the mass of the atom transferred, provides high chemical resolution, even when the efficiency of reaction is relatively low. Examples are given of oxidation, hydroxylation, and chlorination of analyte ions (V+, Fe+, As+, Se+, Sr+, Y+, and Zr+) to improve the capability of determination of complex samples. Preliminary results are given showing O-atom abstraction by CO from CaO+ to enable the determination of Fe in high-Ca samples.