Assessing rare-earth elements and anthropogenic gadolinium in water samples from an urban artificial lake and its tributaries in the Brazilian Federal District

2019 ◽  
Vol 148 ◽  
pp. 27-34 ◽  
Author(s):  
Artur Moraes Amorim ◽  
Fernando Fabriz Sodré ◽  
Tristan C.C. Rousseau ◽  
Poliana Dutra Maia
2013 ◽  
Vol 69 (2) ◽  
pp. 312-319 ◽  
Author(s):  
Cennet Karadaş ◽  
Derya Kara

A new method has been developed for the determination of rare earth elements (REEs) (Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu) in water samples based on preconcentration with a mini-column packed with 6-(2-thienyl)-2-pyridinecarboxaldehyde functionalized Amberlite XAD-4 resin prior to their determination using inductively coupled plasma optical emission spectrometry (ICP-OES). The optimum experimental parameters for preconcentration of REEs, such as pH of the sample, sample and eluent flow rates and sample volume, were investigated. The optimum pH values for quantitative (90–110%) sorption of the REE ions were between 6.0 and 8.0. The elution process was carried out using 2 mL of 1.0 mol L–1 HNO3 solution. Under the optimum conditions, detection limits between 0.032 and 0.963 μg L−1 for a 10 mL sample volume and 0.006 and 0.193 μg L−1 for a 50 mL sample volume were determined. The proposed method was successfully applied to the determination of REEs in water samples with recoveries in the range of 90.1–110.5%.


2013 ◽  
pp. 71-81 ◽  
Author(s):  
Maja Todorovic ◽  
Petar Papic ◽  
Marina Cuk ◽  
Jana Stojkovic

Twenty-one bottled mineral and spring waters from Serbia were analyzed for 16 inorganic chemical parameters, including lanthanides and yttrium which belong to the group of so-called rare earth elements (REE). REE concentrations in the bottled water samples varied over a broad range, from 5.39 to 1585.82 ng/L. Total concentrations in the bottled water samples were calculated taking into account the classification of lanthanides into heavy (HREE) and light (LREE), with yttrium added to the HREE group. The LREE concentrations ranged from 3.62 to 1449.63 ng/L, while those of the HREE were from 0 to 136.19 ng/L. Distinct REE signatures were observed in waters that drained specific rocks. The REE patterns in groundwater from granitic and related rocks showed LREE and HREE enrichment, while groundwater with mafic rock influence exhibited slightly LREE enrichment. Several bottled water samples featured naturally-occurring carbon dioxide, whose solutional capacity contributed to the highest REE concentrations in the analyzed samples. High REE concentrations are also a result of sudden changes in oxidation-reduction conditions, which particularly affect La, Ce and Eu. Aquifers developed in granitic and related rocks (methamorphic and sedimentary rocks) constitute favorable environments for HREE in groundwater, corroborated by the occurrence of HREE in bottled water samples. The bottled water samples largely exhibited a negative cerium anomaly and nearly all the samples showed a positive europium anomaly.


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