Two-Component Model Measurement Error Model in Analytical
Chemistry: Abstract
July 23, 1998
Statistical Engineering Division
Two-Component Model Measurement Error Model in Analytical Chemistry
Professor David M. Rocke
Center for Image Processing and Integrated Computing
The University of California, Davis
Often the standard deviation of analytical errors is assumed to increase
proportionally to the concentration of the analyte, a model that cannot be used
for very low concentrations. For near-zero amounts, the standard deviation is
often assumed constant, which does not apply to larger quantities. Neither
model applies across the full range of concentrations of an analyte. By
positing two error components, one additive and one multiplicative, we obtain a
model that exhibits sensible behavior at both low and high concentration
levels. In this presentation, new data will be presented on the use of maximum
likelihood and weighted least squares to estimate this model and comparisons
will be made of this model to the more conventional model in which the standard
deviation is a linear function of the mean concentration. Example data are
drawn from measurements of organics and metals in water.
Date created: 6/5/2001
Last updated: 6/21/2001
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