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Determination of Iridium in Natural Waters by Clean Chemical Extraction and Negative Thermal Ionization Mass Spectrometry

Anbar, A. D. and Papanastassiou, D. A. and Wasserburg, G. J. (1997) Determination of Iridium in Natural Waters by Clean Chemical Extraction and Negative Thermal Ionization Mass Spectrometry. Analytical Chemistry, 69 (13). pp. 2444-2450. ISSN 0003-2700. https://resolver.caltech.edu/CaltechAUTHORS:20131216-141955489

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Abstract

Methods for the precise, routine measurement of Ir in seawater, riverwater, and estuarine water using isotope dilution negative thermal ionization mass spectrometry (ID-NTIMS) have been developed. After equilibration with a ^(191)Ir-enriched spike, Ir is separated from solution by coprecipitation with ferric hydroxide, followed by anion exchange chromatography using a reductive elution technique. UV irradiation is employed for the decomposition of trace organics, which interfere with negative ion production. IrO_2- ions are produced in the mass spectrometer by heating the sample on a Ni-wire filament in the presence of Ba(OH)_2. Detection efficiencies ranged from 0.1% to 0.3%. We have used these procedures to determine the concentrations of Ir in 4 kg samples from the Pacific Ocean, the Atlantic Ocean, the Baltic Sea, and the rivers supplying the Baltic. Our chemical procedures introduce a total blank of ~2 × 10^8 atoms per sample. The distribution of Ir in the oceans is fairly uniform, averaging ~4 × 10^8 atoms kg^(-1). The concentrations in the rivers supplying the Baltic Sea range from (17.4 ± 0.9) × 10^8 for a pristine river to (92.9 ± 2.2) × 10^8 atoms kg^(-1) for a polluted river. The distribution, speciation, and transport of Ir in natural waters can now be subjected to intensive study.


Item Type:Article
Related URLs:
URLURL TypeDescription
http://dx.doi.org/10.1021/ac961129n DOIArticle
http://pubs.acs.org/doi/abs/10.1021/ac961129nPublisherArticle
ORCID:
AuthorORCID
Wasserburg, G. J.0000-0002-7957-8029
Additional Information:© 1997 American Chemical Society. Received for review November 7, 1996. Accepted February 27, 1997. We are grateful to R. A. Creaser for his critical contributions to the development of the reductive elution technique and for his general assistance in the early stages of this project. We thank M. Anbar and G. R. Rossman for many helpful conversations, especially pertaining to the UV photolysis procedure. ICPMS analyses were performed with the assistance of P. G. Green. T.- L. Ku and J. Chen suggested solvent extraction to purify iron and provided a solvent-extracted sample for testing. This research was supported by Contract No. DOE-DE-FG03-88ER13851 and by an NSF Graduate Research Fellowship to A.D.A. Pacific Ocean sampling was supported by NSF Grant No. OCE-9303094 (R. Lukas) and OCE-9301368 (D. Karl). Atlantic Ocean sampling was assisted by D. Steinberg and other scientists in the BATS program. Baltic Sea sampling was supported by the Swedish Meteorological and Hydrological Institute with the cooperation of P. S. Andersson. Division contribution No. 5689 (944).
Funders:
Funding AgencyGrant Number
Department of Energy (DOE)DE-FG03-88ER13851
NSF Graduate Research FellowshipUNSPECIFIED
NSFOCE-9303094
NSFOCE-9301368
Other Numbering System:
Other Numbering System NameOther Numbering System ID
Caltech Division of Geological and Planetary Sciences5689
Lunatic Asylum Lab944
Issue or Number:13
Record Number:CaltechAUTHORS:20131216-141955489
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20131216-141955489
Official Citation:Determination of Iridium in Natural Waters by Clean Chemical Extraction and Negative Thermal Ionization Mass Spectrometry A. D. Anbar,*,†, D. A. Papanastassiou, and, and G. J. Wasserburg Analytical Chemistry 1997 69 (13), 2444-2450
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:43030
Collection:CaltechAUTHORS
Deposited By: Tony Diaz
Deposited On:17 Dec 2013 00:06
Last Modified:09 Mar 2020 13:19

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