The limit of determination and the limit of nonzero information content

1988 ◽  
Vol 53 (8) ◽  
pp. 1647-1654 ◽  
Author(s):  
Karel Eckschlager

The limit of nonzero information content, which is the lowest result of quantitative determination that is accurate and precise enough to have nonzero information content, is suggested to serve as the lowest limit of applicability of an analytical method whose results involve a systematic error. The limit of determination at which the relative precision of results is σr = 10% can be used as the lowest limit of applicability of a method whose results are accurate.

1988 ◽  
Vol 53 (12) ◽  
pp. 3021-3028 ◽  
Author(s):  
Karel Eckschlager ◽  
Jiří Fusek

It is shown how the information content expressed in terms of the extended divergence measure I(r; p, p0) depends on the amount of the component to be determined when homoscedastic and heteroscedastic dependences of the analytical signal on the amount of the analyte are distinguished. The importance of the accuracy is pointed out, with which the amount of the analyte is known in a reference material employed for testing a particular analytical method. Rules are set, the maintaining of which is aimed at avoiding the origin of null information content of analytical results.


2018 ◽  
Vol 255 ◽  
pp. 182-186 ◽  
Author(s):  
Ana Paula Mörschbächer ◽  
Anja Dullius ◽  
Carlos Henrique Dullius ◽  
Cassiano Ricardo Bandt ◽  
Daniel Kuhn ◽  
...  

1975 ◽  
Vol 58 (5) ◽  
pp. 983-986
Author(s):  
Benny E Knuckles ◽  
Raymond E Miller ◽  
E M Bickoff

Abstract An improved analytical method for the determination of coumestrol in dried alfalfa and leaf protein concentrates is described. In this method, chlorophyll is removed from an alcohol extract prior to the paper chromatographic-fluorometric measurement of coumestrol. Ninety-eight per cent of the coumestrol added to alfalfa leaf protein concentrates is recovered by this method. This improved method gives replicate values with lower standard deviations and coefficients of variation than the literature method.


1985 ◽  
Vol 7 (7) ◽  
pp. 49
Author(s):  
Frida Maciel Pagliosa ◽  
Maria Cladis Mezzomo da Silva ◽  
Maria Elisabeth do Canto Vinadé ◽  
Sonia Maria Bittencourt Frizzo

It was established analytical parameters for steviosides standard, besides the obtainment and purification of theses paramters. The metodology for quantitative determination was proposed for the stevioside analysis in spectrofotometry U.V. The quantitative analysis by spectrofotometry was in 208nm, in ethilic alcool. The curve of calibration presented good relative precision, with analytical error 1.5%. The parameters established in caracterization of standars was: m.p: 197-200 ºC; Rf around of 0.58; maximum absorption in 208nm and molar absortivity higher 4000 in 208nm.


2021 ◽  
Vol 9 (1) ◽  
pp. 40-45
Author(s):  
Carlos Montaño-Osorio ◽  
Dalia Bonilla-Martínez ◽  
Martha Angélica Villegas-González ◽  
Adolfo Eduardo Obaya Valdivia

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