1998
DOI: 10.1016/s0584-8547(98)00105-0
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Simultaneous speciation of selenium and arsenic using elevated temperature liquid chromatography separation with inductively coupled plasma mass spectrometry detection

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Cited by 41 publications
(16 citation statements)
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“…These elements can also be determined in the form of their volatile hydrides by using a type of sample introduction technique called hydride generation (HG) [1,2]. There is a great interest in the field of analytical chemistry in exploring the analytical capabilities of HG with respect to speciation analysis [3][4][5] and multi-element determinations [6,7] since its first use in 1968 by Holak [8].…”
Section: Introductionmentioning
confidence: 99%
“…These elements can also be determined in the form of their volatile hydrides by using a type of sample introduction technique called hydride generation (HG) [1,2]. There is a great interest in the field of analytical chemistry in exploring the analytical capabilities of HG with respect to speciation analysis [3][4][5] and multi-element determinations [6,7] since its first use in 1968 by Holak [8].…”
Section: Introductionmentioning
confidence: 99%
“…Some selected papers studying simultaneous multielemental speciation are listed in Table 2 [201][202][203][204][205]. Since selenium plays important roles in detoxification of both arsenic and mercury, much effort has been expended on the simultaneous speciation of both selenium and mercury species or both selenium and arsenic species by HPLC-ICP-MS [206][207][208]. Solvent extraction with NAA detection for different organohalogen species in biological samples like milk, human tissues, and pine needles has been studied [209][210][211][212][213].…”
Section: Structural Analysismentioning
confidence: 99%
“…The isocratic elution mode and the low concentrations of organic solvent and dissolved solids in the mobile phases permit stable operation of the ICP with no degradation in sensitivity and little matrix interference. Both anion-pairing cations such as tetraethylammonium 101,103,244 or tetrabutylammonium 250,272 and cation-pairing anions such as pentanesulfonate, 269 hexanesulfonate, 244 heptanesulfonate 243,247 and dodecyl sulfonate 272,273 were used for this purpose. 271 A 1.5 cm C 18 guard column placed before the AE column was used to remove most of the organic components from urine that would otherwise bind irreversibly to the packing material.…”
Section: Separation Of Organoarsenic Compoundsmentioning
confidence: 99%