A sustainable and simple energy dispersive X-ray fluorescence method for sulfur determination at trace levels in biodiesel samples via formation of biodiesel spots on a suitable solid support
| Autor: | Ignacio Queralt, Eva Marguí, Martín Resano |
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| Přispěvatelé: | Ministerio de Economía y Competitividad (España), Queralt, Ignacio, Queralt, Ignacio [0000-0002-8790-8382] |
| Jazyk: | angličtina |
| Rok vydání: | 2019 |
| Předmět: |
Accuracy and precision
Materials science Trace Amounts Sample (material) Analytical chemistry chemistry.chemical_element X-ray fluorescence 01 natural sciences Analytical Chemistry Matrix (chemical analysis) 0103 physical sciences Deposition (phase transition) Instrumentation Spectroscopy 010302 applied physics Biodiesel 010401 analytical chemistry Sulfur Atomic and Molecular Physics and Optics 0104 chemical sciences chemistry Preconcentration EDXRF |
| Zdroj: | Zaguán. Repositorio Digital de la Universidad de Zaragoza Consejo Superior de Investigaciones Científicas (CSIC) Digital.CSIC. Repositorio Institucional del CSIC instname |
| Popis: | The aim of the present work is the development of a simple, sensitive and sustainable EDXRF method for the determination of trace amounts of sulfur in biodiesel samples. In this method, the deposition of several microliters of sample onto an organic thin layer and the analysis of the resulting adsorbed biodiesel spot by benchtop EDXRF is proposed. A careful study was performed to select the volume and the best solid support to deposit biodiesel samples, including filters made of different materials (glass fiber, Nylon, cellulose, paper) and a commercial disposable absorbent pad (UltraCarry, Rigaku). A critical issue that limits the use of most of these solid supports was the relative high blank signals that hamper the determination of sulfur at trace levels. Finally, it was found that best strategy was the deposition of 50 μL of biodiesel on the UltraCarry sample retainer. Operating conditions for EDXRF measurements were also evaluated to obtain the best instrumental sensitivity for sulfur determination (Excitation: 20 kV, no primary filter, measurement time: 300 s). Using the best analytical conditions the quantification limit of the method was 7 mg kg−1 of sulfur. This value is even better than the one reported in the ASTM D4294 method (LOQ: 16.0 mg kg−1) but using a sample amount 100 times smaller. The linearity was confirmed in the range of 10–100 mg kg−1by analyzing a set of commercial biodiesel standards. Accuracy and precision of the results, evaluated by the analysis of samples prepared with the same matrix as the standards, with levels of 20, 40 and 75 mg kg−1of sulfur, and processed as unknowns, proved acceptable (Recoveries: 94.3–110.6%, RSD: 10.8–13.6%, n = 3) for the intended purpose. Overall, the performance of the method developed is promising and it could be used to determine trace amounts of sulfur in biodiesel samples in a simple, sustainable and cost-effective way. Furthermore, since the original sample is adsorbed onto a solid support, repeat confirmatory analyses on the same specimen, if needed, can be carried out. © 2019 Elsevier B.V. MR acknowledges the funding obtained via CTQ2015-64684P (MINECO/FEDER) and from the Aragón Government (Fondo Social Europeo). Authors would like to acknowledge to Mr. Arnau Ortiz for his contribution on the performance of the experimental work. |
| Databáze: | OpenAIRE |
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