scholarly journals Determination of Inorganic Arsenic(III) and Arsenic(V) in Water Samples by Ion Chromatography/Inductively Coupled Plasma-Mass Spectrometry

2007 ◽  
Vol 90 (1) ◽  
pp. 284-290 ◽  
Author(s):  
Yiu-Chung Yip ◽  
Hei-Shing Chu ◽  
Chung-Fai Yuen ◽  
Wing-Cheong Sham
Keyword(s):  
Mass Spectrometry ◽  
Ion Chromatography ◽  
Water Samples ◽  
Inductively Coupled Plasma ◽  
New York State ◽  
Sample Preservation ◽  
Inductively Coupled ◽  
Relative Standard ◽  
Plasma Mass Spectrometry

Abstract A method was validated for the direct determination of As(III) and As(V) in water samples by ion chromatography/inductively coupled plasma-mass spectrometry. Sample preservation required only dilution with a mobile phase containing a sufficient amount of ethylenediaminetetraacetic acid and acetic acid. Analyses of 6 certified reference materials (CRMs) of various water matrixes, including seawater, demonstrated good method accuracy. The matrixes included 2 natural water samples National Institute of Standards and Technology Standard Reference Material (NIST SRM) 1643e and NIST SRM 1640, 1 fortified standard solution (TMDA-64), 1 fortified water sample (TM-DWS), and 2 seawater samples (CASS-4 and NASS-5). The sum of As(III) and As(V) in each CRM agreed with the respective certified value for the total amount of As within its stated uncertainty. Quantitative recoveries (96.7-102.1%) were obtained. Satisfactory results were achieved for intraday repeatability relative standard deviation (RSD 0.3-5.1%] and interday precision (RSD 0.7-4.1%). In the study of fortified blanks and fortified CRMs, quantitative recoveries of As(III) and As(V) (92.5-102.6%) were obtained. Interconversion of As(III) and As(V) was not observed under the conditions of sample preservation. International comparability of analytical results was demonstrated by the analysis of 2 interlaboratory proficiency test samples, NY7011 and NY8511, from the New York State Department of Health.

scholarly journals tudy on the determination of ¹⁰B/¹¹B isotope ratio in water samples by isotope dilution – inductively coupled plasma mass spectrometry (ID-ICPMS)

2021 ◽  
Vol 7 (3) ◽  
pp. 8-16
Author(s):  
Kim Dung Nguyen Thi ◽  
Thi Lien Nguyen
Keyword(s):  
Mass Spectrometry ◽  
Isotope Dilution ◽  
Water Samples ◽  
Inductively Coupled Plasma ◽  
Isotope Ratio ◽  
Isotopic Ratio ◽  
Primary Coolant ◽  
Inductively Coupled ◽  
Plasma Mass Spectrometry

The determination of 10B/11B isotope ratio and boron concentration in various watersamples using isotope dilution technique with inductively coupled plasma mass spectrometry (ICPMS) was studied. The interferences on precision and accuracy in isotopic ratio determination by ICPMS such as memory effects, dead time, spectral overlap of 12C were investigated for the selection of optimum conditions. By the addition of certain amounts of enriched 10B into samples, the 10B/11B ratio was determined through ICP-MS signal of 10B and 11B. The detection limit for 10B and 11B was experimentally obtained as 0.26 µg/L and 0.92 µg/L, respectively. The ratios of 10B/11B in measured water samples varied in the ranged between 0.1905 and 0.2484 for different matrices. This method has been then applied for the determination of boron isotopic ratio in VVER-1000 reactor-type simulated primary coolant water and in some environmental water samples.

scholarly journals Determination of Arsenic, Cadmium, Mercury, and Lead by Inductively Coupled Plasma/Mass Spectrometry in Foods after Pressure Digestion: NMKL Interlaboratory Study

2007 ◽  
Vol 90 (3) ◽  
pp. 844-856 ◽  
Author(s):  
Kaare Julshamn ◽  
Amund Maage ◽  
Hilde Skaar Norli ◽  
Karl H Grobecker ◽  
Lars Jorhem ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Inductively Coupled Plasma ◽  
Method Performance ◽  
Inductively Coupled ◽  
Icp Ms ◽  
Relative Standard ◽  
Limit Of Quantitation ◽  
Plasma Mass Spectrometry ◽  
Standard Deviations

Abstract Thirteen laboratories participated in an interlaboratory method performance (collaborative) study on a method for the determination of arsenic, cadmium, mercury, and lead by inductively coupled plasma/mass spectrometry (ICP/MS) after pressure digestion including the microwave heating technique. Prior to the study, the laboratories were able to practice on samples with defined element levels (pretrial test). The method was tested on a total of 7 foodstuffs: carrot puree, fish muscle, mushroom, graham flour, simulated diet, scampi, and mussel powder. The elemental concentrations in mg/kg dry matter (dm) ranged from 0.0621.4 for As, 0.0328.3 for Cd, 0.040.6 for Hg, and 0.012.4 for Pb. The materials used in the study were presented to the participants as blind duplicates, and the participants were asked to perform single determinations on each sample. The repeatability relative standard deviations (RSDr) for As ranged from 3.8 to 24%, for Cd from 2.6 to 6.9%, for Hg from 4.8 to 8.3%, and for Pb from 2.9 to 27%. The reproducibility relative standard deviations (RSDR) for As ranged from 9.0 to 28%, for Cd from 2.8 to 18%, for Hg from 9.9 to 24%, and for Pb from 8.0 to 50%. The HorRat values were less than 1.5 for all test samples, except for the determination of Pb in wheat flour at a level close to the limit of quantitation (0.01 mg/kg dm). The study showed that the ICP/MS method is satisfactory as a standard method for elemental determinations in foodstuffs.

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