Determination of chromium in water and urine by reaction cell inductively coupled plasma mass spectrometry

Citation
Yl. Chang et Sj. Jiang, Determination of chromium in water and urine by reaction cell inductively coupled plasma mass spectrometry, J ANAL ATOM, 16(12), 2001, pp. 1434-1438
Citations number
24
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences
Journal title
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY
ISSN journal
02679477 → ACNP
Volume
16
Issue
12
Year of publication
2001
Pages
1434 - 1438
Database
ISI
SICI code
0267-9477(2001)16:12<1434:DOCIWA>2.0.ZU;2-D
Abstract
An inductively coupled plasma mass spectrometry (ICP-MS) instrument equippe d with a dynamic reaction cell (DRC) was used for the determination of chro mium in water and urine samples. The effect of the operating conditions of the DRC system was studied to get the best signal-to-noise ratio. The poten tially interfering (ArC+)-Ar-40-C-12, (ClOH+)-Cl-35-O-16, (SO)-S-34-O-18, ( ArCH+)-Ar-40-C-12 and (ClO+)-Cl-37-O-16 ions at the chromium masses m/z 52 and 53 were reduced in intensity by approximately 2-3 orders of magnitude b y using 1.0 ml min(-1) NH3 as reaction cell gas in the DRC while a q value of 0.6 was used. The limits of detection for Cr-52 and Cr-53 were 0.015 and 0.024 ng ml(-1) Cr, respectively. This method was applied to determine Cr in NRCC SLRS-3 Riverine Water reference sample, NIST SRM 1643d Trace Elemen ts in Water, NIST SRM 2670 Urine reference sample and several water and uri ne samples collected locally. The external calibration method and isotope d ilution method were used for the determination of Cr in selected samples. T he results for the reference samples agreed satisfactorily with the referen ce values. Results for other samples analyzed by different quantitation met hods agreed satisfactorily. Precision between sample replicates was better than 20% for most of the determinations.