2013
DOI: 10.1016/j.talanta.2013.06.046
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Optimization of the arsenazo-III method for the determination of uranium in water and plant samples

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Cited by 33 publications
(9 citation statements)
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“…The Environmental Protection Agency (EPA) limits the level of uranium in drinking water as 30 lg L -1 [1]. This maximum contaminant level is consistent with WHO recommendation value [3]. This stringent level regulation made scientist develop new analytical techniques for accurate determination uranium in trace levels in water samples.…”
Section: Introductionsupporting
confidence: 56%
See 1 more Smart Citation
“…The Environmental Protection Agency (EPA) limits the level of uranium in drinking water as 30 lg L -1 [1]. This maximum contaminant level is consistent with WHO recommendation value [3]. This stringent level regulation made scientist develop new analytical techniques for accurate determination uranium in trace levels in water samples.…”
Section: Introductionsupporting
confidence: 56%
“…It can be naturally found in environmental soil, rock, air and water samples [2]. According to Jouberty et al [3], it is slightly radioactive element in its natural state, but it is nonetheless harmful to body. The Environmental Protection Agency (EPA) limits the level of uranium in drinking water as 30 lg L -1 [1].…”
Section: Introductionmentioning
confidence: 99%
“…The potentials were measured by using the electrode cell assembly under optimized conditions described in this work and calibration plots were further employed to evaluate the concentration of UO 2 2+ in these samples. The results were validated using the results of the analyses of the same samples by applying Arsenazo III spectrophotometric method and the results obtained are presented in Table . As can be seen, the results obtained from both techniques are comparable, indicating the applicability of the developed electrode for accurate and precise determination of UO 2 2+ content in real samples.…”
Section: Resultsmentioning
confidence: 99%
“…Content of U (VI) was determined by the arsenazo (III) staining method [29]. 1 mL of sample was added to 1 mL of arsenazo (III) chromogenic agent, the volume of the mix was adjusted to 10 mL with 0.4 mol/L chloroacetic acid-sodium chloroacetate buffer, then the mix was shaken and left to incubate at room temperature for 30 min.…”
Section: Methodsmentioning
confidence: 99%