Development of international key comparisons in the field of chemico-analytical measurements

2021 ◽  
pp. 65-72
Author(s):  
Leonid А. Konopelko ◽  
Yuri А. Kustikov ◽  
Mikhail V. Okrepilov ◽  
Anna V. Kolobova ◽  
Pavel V. Migal ◽  
...  

The most challenging goals in the field of chemico- and bioanalytical measurements are described. Solutions of these problems are presented, which are being solved in particular by participating in new international comparisons organized by the Cosultative Committee on the Amount of Substance of the International Committee on Weights and Measures (CCQM CIPM). The purposes and tasks of developing key comparisons in the following areas are described: isotopic measurements; determination of the purity of substances; organic analysis; bioanalytical measurements; measurements of aerosol particle parameters; measurements in the field of gas analysis and electrochemistry. It is shown that participation in international key comparisons makes it possible to obtain valid and reliable results of measurements of the composition and properties of gas and liquid media, as well as solid substances and materials.

2001 ◽  
Vol 73 (6) ◽  
pp. 927-931 ◽  
Author(s):  
René Dybkær

Expressing the amount of a catalyst is often most conveniently done by assessing its catalytic effect. Under zero-order kinetics the catalyzed rate of conversion for a specified reaction is constant and proportionate to the amount-of-substance concentration of catalyst present. Defining the kind-of-quantity "catalytic activity" as a property of the catalyst measured by the catalyzed rate of conversion, the coherent SI unit is mole per second. Following thorough discussions in the IUPAC, the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC), the International Union of Biochemistry and Molecular Biology (IUBMB), and the World Health Organization (WHO), a petition was presented by the IFCC to the International Committee for Weights and Measures (CIPM) on a special name "katal", symbol kat, for "mole per second" when used in measuring catalytic activity. This request was granted by the General Conference for Weights and Measures (CGPM) by Resolution 12 (1999). Hereafter, the coherent SI unit katal = 1 mol s­1 should replace the off-system IUB unit "(enzyme) unit" = 1 mmol min­1 16.67 nkat. Thus, by suitable definition of reaction conditions, results for catalytic activity and derivative kinds-of-quantity are metrologically traceable to the SI.


2020 ◽  
pp. 26-32
Author(s):  
M. I. Kalinin ◽  
L. K. Isaev ◽  
F. V. Bulygin

The situation that has developed in the International System of Units (SI) as a result of adopting the recommendation of the International Committee of Weights and Measures (CIPM) in 1980, which proposed to consider plane and solid angles as dimensionless derived quantities, is analyzed. It is shown that the basis for such a solution was a misunderstanding of the mathematical formula relating the arc length of a circle with its radius and corresponding central angle, as well as of the expansions of trigonometric functions in series. From the analysis presented in the article, it follows that a plane angle does not depend on any of the SI quantities and should be assigned to the base quantities, and its unit, the radian, should be added to the base SI units. A solid angle, in this case, turns out to be a derived quantity of a plane angle. Its unit, the steradian, is a coherent derived unit equal to the square radian.


1980 ◽  
Vol 53 (3) ◽  
pp. 437-511 ◽  
Author(s):  
D. W. Brazier

Abstract An attempt has been made to review the development of thermoanalytical procedures as they have been applied to elastomers and elastomer systems over the past 10 years. For all rubber industry products, temperature and its effects, either alone or in conjunction with the chemical environment, play an important role from the production stage through to the final failure of the product in the field. It is thus not surprising that thermal analysis, in which temperature is the prime variable, has found such diverse applications in elastomer studies. The identification and quantitative analysis of rubber formulations have received most attention. Such formulations produce characteristic “fingerprints” when studied in DTA, DSC, TG, or TMA. In DSC, the determination of the glass transition characteristics, the observation and determination of crystallinity, the detection of cyclization reactions, and the monitoring of thermal and oxidative degradation characteristics can all be observed in a single experiment covering the temperature range from −150 to +600°C. At normal heating rates, e.g., 20°C/min, such information is available in 40 min. TG/DTG analysis can yield the elastomer or elastomers content, oil and plasticizer, carbon black (level and often type), and inorganic ash in less than 60 min. Processing and curing can also be studied. Blend compatibility can be assessed on the basis of both Tg and crystallinity measurements and the data used to determine optimum mixing times. Sulfur vulcanization and peroxide curing of elastomers is readily monitored by DSC and can be used for confirmation analysis of the presence of curatives. Limitations in such analysis exist, but as understanding and ability to interpret cure exotherms increase, valuable information about the mechanism and the nature of the cured network will be obtained. The testing of rubber compounds involves many hours of labor by current procedures. The rapidity of thermal analysis promises to offer some relief. In addition to DSC and TG, TMA, a relatively new technique, offers a rapid approach to low-temperature testing. Dynamic mechanical analysis (DMA) offers a rapid route to determining dynamic properties, but as yet, relatively little has been published on the application of this new technique to elastomers. As environmental concern increases, techniques such as evolved gas analysis (EGA) and combined techniques such as TG/gas chromatography are predicted to play an important role. As for the future, it is readily apparent that the principles of the methods have been established and, in several cases, it now remains to reduce them to a practical level. In some areas, such as vulcanization studies, much remains to be undertaken to improve our interpretive skills. Although there is some indication that certain industries have produced “in-house” standards for the analysis of rubber compounds by DSC and TG/DTG, it will only be when national and international standards organizations study and produce standard procedures, that the techniques will be generally adopted. Maurer's prediction in 1969 of increased applications of DTA and TG in elastomer studies has undoubtedly proved correct, and with the proliferation of reliable commercial instrumentation, significant developments can be anticipated in the next decade.


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