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Matrix effects using an ICP-MS with a single positive ion lens and grounded stop: analyte mass dependent?

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Abstract

Matrix effects in ICP-MS are generally considered to be more severe for heavy matrix elements and light analyte elements, consistent with space charge repulsion of ions during their travel from the plasma to the mass analyzer. However, the severity of matrix-induced changes in analyte sensitivity as a function of analyte mass may depend on the ion optics design, voltages applied to the ion optics and plasma parameters (robustness). Comprehensive characterization of matrix effects using an instrument with ion optics consisting of a grounded stop, a single positive cylindrical lens and a grounded aperture prior to the RF quadrupole is described. Matrix effects were studied as a function of analyte mass, matrix mass, matrix element concentration, lens voltage, and nebulizer gas flow rate. The effects of high concentrations of a wide mass range of matrix elements (Na, Cu, Y, In, Cs, Tb, Lu, and Tl) on analyte sensitivities with a wide range of masses (7Li+, 11B+, 24Mg+, 45Sc+, 60Ni+, 71Ga+, 75As+, 88Sr+, 111Cd+, 138Ba+, 153Eu+, 172Yb+, 209Bi+, and 238U+) were investigated. Matrix effects for equimolar matrix element concentrations were more severe as the matrix element mass increased. However, the severity of matrix effects depended less on the analyte ion mass than expected. Furthermore, matrix effects on high mass analyte sensitivities were more severe than those reported for first generation ICP-MS instruments.

Graphical abstract: Matrix effects using an ICP-MS with a single positive ion lens and grounded stop: analyte mass dependent?

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Publication details

The article was received on 28 Jan 2017, accepted on 15 Mar 2017 and first published on 17 Mar 2017


Article type: Paper
DOI: 10.1039/C7JA00043J
Citation: J. Anal. At. Spectrom., 2017, Advance Article
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    Matrix effects using an ICP-MS with a single positive ion lens and grounded stop: analyte mass dependent?

    J. W. Olesik and S. Jiao, J. Anal. At. Spectrom., 2017, Advance Article , DOI: 10.1039/C7JA00043J

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