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Automated determination of gallium in seawater using seaFAST pre-concentration and high-resolution inductively-coupled plasma mass spectrometry.

作者信息

Gilbert Melissa, Ho Peng, Whitmore Laura, Shiller Alan

机构信息

University of Southern Mississippi, 1020 Balch Blvd Stennis Space Center, MS, 39529, USA.

University of Southern Mississippi, 1020 Balch Blvd Stennis Space Center, MS, 39529, USA.

出版信息

Anal Chim Acta. 2023 Feb 8;1241:340799. doi: 10.1016/j.aca.2023.340799. Epub 2023 Jan 3.

DOI:10.1016/j.aca.2023.340799
PMID:36657873
Abstract

There has been increased interest in dissolved gallium (Ga) in natural waters due to its long residence time and its usefulness in tracking water masses; however, current analytical approaches are time consuming and labor intensive (e.g., magnesium hydroxide co-precipitation method, (Mg(OH))) or have concerns such as carryover and sample recovery (automated resin column extraction). Ocean observing programs, such as GEOTRACES, recover hundreds of samples per expedition. There are both logistical (sample volume) and analytical (person-hour) demands to economically collect and analyze Ga. We present an automated isotope dilution method (using 99.8% enriched Ga) to determine Ga in seawater utilizing commercially available equipment while addressing the challenges of a) sample volume and sample pre-concentration factor, b) instrumental interferences, c) sample-sample carryover, d) sample recovery variability, and e) improving sample detection limits, accuracy and precision. A seaFAST SC-4DXS pico (Elemental Scientific, Inc.; ESI) was used to pre-concentrate 20 mL of sample on a Nobias PA1 resin column 67-fold before analysis in medium resolution on a ThermoFisher high-resolution inductively-coupled plasma mass spectrometer (HR-ICP-MS) equipped with an APEX Q FAST enabled spray chamber (ESI) to increase signal intensity and decrease instrument interferences. The new automated seaFAST method reproduced Ga concentrations determined by the Mg(OH) method, but with greater precision (RSD <4%) and a lower detection limit (0.10 pmol L). This method is ideal for high throughput applications and can be easily implemented using commercially available equipment.

摘要

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