Abstract

A computational and experimental method of certification and arrangement of intra laboratory control of the methods for analysis of air environment, i.e., air of the working zone, atmosphere air and industrial emissions into the atmosphere, is developed. Note that nowadays a rather small number of standard samples (SS) of air environment (calibration gas mixtures (CGM)) is available for less than thirty substances with determined maximum permissible concentrations (MPC) (inorganic gases and light organic compounds). About 100 sources of microcflows (MF) are also developed for light organic compounds. Such a narrow set of developed SS hinders determination of the accuracy indicators on the basis of the certification experiment for the vast majority of the methods used for analysis of air samples and, in turn, keeps out of stating standards for intra-laboratory control and implementation of the procedures of operational control and control of the stability. For those techniques (in the lack of calibration gas mixtures and sources of microflows), the error characteristics are estimated usually by calculations with exception of the stability of the calibration curves and error characteristics of the individual sampling stages which are determined experimentally. The proposed method implies a conditional division of the technique into two stages: sampling and analytical stages. For the stage of sampling, the error characteristics are determined by the calculation-experimental method, for the analytical stage, by the experimental method, similar to other methods for analysis of condensed media. The possibility of arrangement of the intra-laboratory control of the analytical stage and implementation of all the algorithms of both operational and stability control, including construction of Shewhart’s control charts is shown. The proposed method makes it possible to arrange certification of the majority of similar techniques used in the sphere of state regulation of ensuring the uniformity of measurements that have not been previously certified and provided with standard samples in the form of calibration gas mixtures and sources of microflows.

Highlights

  •  äàííîé ðàáîòå ïðåäëîæåí ðàñ÷åòíî-ýêñïåðèìåíòàëüíûé ìåòîä àòòåñòàöèè è îðãàíèçàöèè âíóòðèëàáîðàòîðíîãî êîíòðîëÿ ìåòîäèê àíàëèçà âîçäóøíûõ ñðåä — âîçäóõà ðàáî÷åé çîíû, àòìîñôåðíîãî âîçäóõà è ïðîìûøëåííûõ âûáðîñîâ â àòìîñôåðó

  • About 100 sources of microcflows (MF) are developed for light organic compounds. Such a narrow set of developed SS hinders determination of the accuracy indicators on the basis of the certification experiment for the vast majority of the methods used for analysis of air samples and, in turn, keeps out of stating standards for intra-laboratory control and implementation of the procedures of operational control and control of the stability

  • The proposed method implies a conditional division of the technique into two stages: sampling and analytical stages

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Summary

Introduction

 äàííîé ðàáîòå ïðåäëîæåí ðàñ÷åòíî-ýêñïåðèìåíòàëüíûé ìåòîä àòòåñòàöèè è îðãàíèçàöèè âíóòðèëàáîðàòîðíîãî êîíòðîëÿ ìåòîäèê àíàëèçà âîçäóøíûõ ñðåä — âîçäóõà ðàáî÷åé çîíû, àòìîñôåðíîãî âîçäóõà è ïðîìûøëåííûõ âûáðîñîâ â àòìîñôåðó. Òàêîé óçêèé íàáîð ðàçðàáîòàííûõ ÑÎ íå ïîçâîëÿåò óñòàíîâèòü íà îñíîâå àòòåñòàöèîííîãî ýêñïåðèìåíòà ïîêàçàòåëè òî÷íîñòè äëÿ ïîäàâëÿþùåãî áîëüøèíñòâà ìåòîäèê àíàëèçà ïðîá âîçäóøíûõ ñðåä è íà îñíîâå íàéäåííûõ ïîêàçàòåëåé òî÷íîñòè óñòàíîâèòü íîðìàòèâû âíóòðèëàáîðàòîðíîãî êîíòðîëÿ, à òàêæå ðåàëèçîâàòü ïðîöåäóðû îïåðàòèâíîãî êîíòðîëÿ è êîíòðîëÿ ñòàáèëüíîñòè.

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