2001
DOI: 10.1016/s0003-2670(01)01301-0
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On-line removal of Ca, Na and Mg from iminodiacetate resin for the determination of trace elements in seawater and fish otoliths by flow injection ICP-MS

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Cited by 43 publications
(26 citation statements)
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“…The column-conditioning step removes any residual acid that remains from the previous sample elution step and ensures that the resin is no longer in the protonated form, which might otherwise reduce retention of the analyte and thereby lessen the sensitivity of the method. Willie et al (2001) demonstrated that a 0.1-M ammonium acetate rinse Detection limit (UHP water), pM 3.8 5 (Cannizzaro et al 2000) Linear range, pM 3.8-2000 5-850 pM (Cannizzaro et al 2000) Blanks, pM 4.2 ± 1.5…”
Section: Assessmentmentioning
confidence: 99%
“…The column-conditioning step removes any residual acid that remains from the previous sample elution step and ensures that the resin is no longer in the protonated form, which might otherwise reduce retention of the analyte and thereby lessen the sensitivity of the method. Willie et al (2001) demonstrated that a 0.1-M ammonium acetate rinse Detection limit (UHP water), pM 3.8 5 (Cannizzaro et al 2000) Linear range, pM 3.8-2000 5-850 pM (Cannizzaro et al 2000) Blanks, pM 4.2 ± 1.5…”
Section: Assessmentmentioning
confidence: 99%
“…Acidified samples were UV-oxidized for 30 min prior to analysis. Trace metals were then concentrated on the resin at the appropriate pH and eluted with 1 M QHNO 3 (Willie et al, 1998;Warnken et al, 2000;Willie et al, 2001;Ndung'u et al, 2003). The filtrates were loaded onto the resin column for 2 min for medium resolution analytes ( 56 Fe, 59 Co, 63 Cu, and 66 Zn) at a pH of 5.5 with an ammonium acetate buffer and 30 s for low resolution analytes ( 55 Mn, 111 Cd) at a pH of 8.9 with an ammonium chloride buffer in separate analyses (Hurst and Bruland, 2007).…”
Section: Particulate and Dissolved Trace Metal Analysesmentioning
confidence: 99%
“…Currently, isotope dilution inductively coupled plasma mass spectrometry appears to be a method of choice and several successful reports of its use for the accurate and precise characterization for otolith material have appeared. [7][8][9][10][11] However, research in this area has generally been impeded by a lack of certified reference materials for analytical quality assurance. The National Institute for Environmental Studies (NIES), Environment Agency of Japan, recently released a fish otolith reference material certified for Na, Mg, K, Sr and Ba for this purpose, 9 but there remains a need not only for complementary materials, but for materials which are certified for additional trace heavy metals that can serve as additional markers to extend the usefulness of otolith composition for fisheries studies.…”
Section: Introductionmentioning
confidence: 99%