Method validation and uncertainty for the determination of rare earth elements, yttrium, thorium and phosphorus in monazite samples by ICP-OES

2019 ◽  
Author(s):  
Chem Int

A method is described for the inductively coupled plasma optical emission spectrometric (ICP-OES) determination of rare earth elements (REE), yttrium (Y), thorium (Th) and phosphorus (P) in monazite samples. Sample preparation was carried out by fuming with sulphuric acid followed by fluoride fusion of the remaining residue. The method was validated using the single laboratory approach by assessment of analytical performance characteristics like specificity, linearity, range, accuracy and precision. Spectral interferences were observed in the case of some heavy REE (Ho,Er,Tm) by light REE (Nd) and correction factors were deduced and applied. The limit of quantification, instrument linearity and the method range were evaluated. Relative standard deviation (RSD) values ranging from 2.6 to 10.2 % were obtained for repeatability studies and RSD values ranging from 1.7 to 11.1% for intra-lab reproducibility studies. Accuracy was established by application to a monazite certified reference material (CRM) and also through comparison of results obtained by present method with those obtained by an alternate method. The validation results were compliant with the acceptance criteria for the various parameters assessed. A simple procedure has been described for the estimation of associated measurement uncertainty using the GUM “bottom-up” modelling approach and results presented in this paper. The validated method was applied to the determination of REE, Y, Th and P in some monazite samples from India.

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%.


2020 ◽  
Vol 11 (2) ◽  
pp. 160-167
Author(s):  
Mohammed Jamaluddin Ahmed ◽  
Faisal Hossain ◽  
Esham Mahmood

A simple, ultra-sensitive, and highly selective spectrophotometric method has been established for the trace quantification of zinc (Zn), using 2-hydroxynaphthaldehyde benzoylhydrazone (HNABH). Zn forms a pale yellowish-green complex (maximum absorption at 426 nm) with HNABH (1:1, v:v) in a marginally acidic solution (0.00005-0.00023 M H2SO4). The average molar absorption coefficient and Sandell’s sensitivity were found: 2.87×105 L/mol.cm and 12 ng/cm2 of Zn, respectively. The observed linearity range for Zn was 0.01-50 mg/Lwith a detection limit of 1 µg/L. The analysis of biological, food, and vegetable samples using the suggested method were found to be in tremendous accord with those acquired by Atomic Absorption Spectroscopy (AAS) and Inductively Coupled Plasma-Optical Emission Spectroscopy (ICP-OES). The method has high precision and accuracy (s = ±0.01 for 0.5 mg/L). The limit of quantification of the proposed method was 10 µg/L.


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