Certified reference material of bioethanol for metrological traceability in electrochemical parameters analyses

Talanta ◽  
2012 ◽  
Vol 99 ◽  
pp. 99-103 ◽  
Author(s):  
Isabel Cristina Serta Fraga ◽  
Carla Matos Ribeiro ◽  
Sidney Pereira Sobral ◽  
Júlio Cesar Dias ◽  
Mary Ane Gonçalves ◽  
...  
2018 ◽  
Vol 15 (29) ◽  
pp. 243-250
Author(s):  
D. E. GONÇALVES ◽  
J. F. S. GOMES ◽  
A. P. D. ALVARENGA ◽  
T. de O. ARAUJO ◽  
P. P. BORGES

The use of certified reference material (CRM) in chemical analyzes is an important requirement in quality assurance systems, since it allows the metrological traceability of results, thus achieving valid and comparable results. This work describes the development and production of holmium oxide reference material that, after certification, will be used in the calibration of the wavelength range of UV-Vis spectrometers and also the necessary feasibility studies to establish the measurement parameters to be used in the next steps of the material production and certification.


2019 ◽  
Vol 14 (3-4) ◽  
pp. 17-32 ◽  
Author(s):  
A. G. Budko ◽  
A. Y. Mikheeva ◽  
A. I. Krylov

The paper presents information on the development of a new certified reference material (CRM) for mass fraction of dioxins in animal fat, with established metrological traceability. A procedure for preparing and certifying CRM material is given. The GC–LRMS method with isotopic dilution was used as an analytical method for establishing certified characteristics. The uncertainties due to inhomogeneity and instability of the CRM material were estimated in order to account for their contribution to the uncertainty of certified values. In addition, the results of interlaboratory comparisons (ILC) for an experimental batch of the developed CRM are presented. Measurement results provided by ILC participants are shown to be in good agreement with the certified characteristics of the CRM. The certified values of dioxin mass fractions (PCDF group) in the CRM material are established to vary from 1 to 1000 ng / kg, with the relative expanded uncertainty ranging from 10 to 20 %.


2020 ◽  
Vol 66 (6) ◽  
pp. 769-778 ◽  
Author(s):  
W Greg Miller ◽  
Jeffrey Budd ◽  
Neil Greenberg ◽  
Cas Weykamp ◽  
Harald Althaus ◽  
...  

Abstract Establishing metrological traceability to an assigned value of a matrix-based certified reference material (CRM) that has been validated to be commutable among available end-user measurement procedures (MPs) is central to producing equivalent results for the measurand in clinical samples (CSs) irrespective of the clinical laboratory MPs used. When a CRM is not commutable with CSs, the bias due to noncommutability will be propagated to the CS results causing incorrect metrological traceability to the CRM and nonequivalent CS results among different MPs. In a commutability assessment, a conclusion that a CRM is commutable or noncommutable for use with a specific MP is made when the difference in bias between the CRM and CSs meets or does not meet a criterion for that specific MP when compared to other MPs. A conclusion regarding commutability or noncommutability requires that the magnitude of the difference in bias observed in the commutability assessment remains unchanged over time. This conclusion requires the CRM to be stable and no substantive changes in the MPs. These conditions should be periodically reverified. If an available CRM is determined to be noncommutable for a specific MP, that CRM can be used in the calibration hierarchy for that MP when an appropriately validated MP-specific correction for the noncommutability bias is included. We describe with examples how a MP-specific correction and its uncertainty can be developed and applied in a calibration hierarchy to achieve metrological traceability of results for CSs to the CRM’s assigned value.


Minerals ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 92
Author(s):  
Said Kounbach ◽  
Mokhtar Ben Embarek ◽  
Abdeljalil Chemaa ◽  
Rachid Boulif ◽  
Rachid Benhida ◽  
...  

Fluosilicic acid is a by-product of the chemical phosphate industry, mainly during the manufacture of phosphoric acid and triple super phosphate (TSP). To ensure the accurate measurement of the H2SiF6 mass fraction in this by-product, method validation is required, which needs a certified reference material (CRM) with its traceability to the International System of Units (SI). This work describes the development of a certified reference material of fluosilicic acid, which is commercially unavailable. Details of all steps, such as sample preparation, homogeneity and stability studies, value assignment, establishment of metrological traceability, and uncertainty estimation of the certified reference material, are fully described. The H2SiF6 mass fraction in the CRM was quantified by two analytical methods, i.e., UV-VIS as a primary method of analysis and flame mode atomic absorption spectroscopy (AAS) as a second method. It is worth noting that the results obtained from each method were in good agreement. The CRM certified value and corresponding expanded uncertainty, obtained from the combined standard uncertainty multiplied by the coverage factor (k = 2), for a confidence interval of 95%, was (91.5 ± 11.7) g·kg−1. The shelf life of the developed CRM is determined to be 1 year, provided that storage conditions are ensured. The developed CRM can be applied to validate analytical methods, improve the accuracy of measurement data as well as to establish the meteorological traceability of analytical results.


2011 ◽  
Vol 400 (3) ◽  
pp. 821-833 ◽  
Author(s):  
Pearse McCarron ◽  
Håkan Emteborg ◽  
Cíara Nulty ◽  
Thomas Rundberget ◽  
Jared I. Loader ◽  
...  

Molecules ◽  
2021 ◽  
Vol 26 (14) ◽  
pp. 4370
Author(s):  
Liping Fang ◽  
Linyan Huang ◽  
Gang Yang ◽  
Yang Jiang ◽  
Haiping Liu ◽  
...  

Water matrix certified reference material (MCRM) of volatile organic compounds (VOCs) is used to provide quality assurance and quality control (QA/QC) during the analysis of VOCs in water. In this research, a water MCRM of 28 VOCs was developed using a “reconstitution” approach by adding VOCs spiking, methanol solution into pure water immediately prior to analysis. The VOCs spiking solution was prepared gravimetrically by dividing 28 VOCs into seven groups, then based on ISO Guide 35, using gas chromatography-mass spectrometry (GC-MS) to investigate the homogeneity and long-term stability. The studies of homogeneity and long-term stability indicated that the batch of VOCs spiking solution was homogeneous and stable at room temperature for at least 15 months. Moreover, the water MCRM of 28 VOCs was certified by a network of nine competent laboratories, and the certified values and expanded uncertainties of 28 VOCs ranged from 6.2 to 17 μg/L and 0.5 to 5.3 μg/L, respectively.


MAPAN ◽  
2017 ◽  
Vol 32 (3) ◽  
pp. 215-222
Author(s):  
H. E. Ahmed ◽  
Mohamed Hassan ◽  
Mohamed Nour ◽  
A. B. Shehata ◽  
Maher Helmy

2010 ◽  
Vol 53 (4) ◽  
pp. 1037-1041 ◽  
Author(s):  
Sooyeun Lee ◽  
Hajime Miyaguchi ◽  
Eunyoung Han ◽  
Eunmi Kim ◽  
Yonghoon Park ◽  
...  

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