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Model Based Chemical Analyses. Model Based Analyses.
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Model Based Analyses The very rigid constraints of a chemical model form a framework within which the fit is confined and which results in a robust analysis, in model-free analysis, this framework is dramatically wider and looser and these methods suffer gradually from a sever lack of robustness. It must be remembered, however, that the choice of the wrong model necessarily results in the rung analysis and wrong resulting parameters.
k A B d[A] = -k [A] dt [A]0=1 k=0.2 Simple first order kinetics [A] = [A]0 exp (-kt) [B] = [A]0 (1 - exp (-kt))
Selective region for B Selective region for A
Univariate data Al=440 = eA [A]0 exp (-kt) + r Al=540 = eB [A]0 (1 - exp (-kt)) + r
How one can determine the parameters of the model? ^ Al=440 = eA [A]0 exp (-kt) + r Suppose eA=1.3 & k=0.25
How one can determine the parameters of the model? ^ Al=440 = eA [A]0 exp (-kt) + r Suppose eA=1.3 & k=0.25 RSS = S (ri2) RSS =0.15
How one can determine the parameters of the model? ^ Al=440 = eA [A]0 exp (-kt) + r Suppose eA=1.0 & k=0.20 RSS =1.42 × 10-5
0.5 < eA < 1.5 & 0.1 < k < 0.3
0.5 < eA < 1.5 & 0.1 < k < 0.3
Direct Fitting Kinfit1.m
? Modify the kinfit1 function for fitting a kinetic curve which is selective for product.
eA Linear Parameters Al=440 = eA [A]0 exp (-kt) + r = + y x eA = + r r= f (k) eA = (yTy)-1 yT x
? Investigate the effects of non-correct value of initial concentration on the results of analysis.
Selective multivariate data Al1 = eA1 {[A]0 exp (-kt)} + rl1 eA1 = + eA1 eA2 Al2 = eA2 {[A]0 exp (-kt)} + rl2 = + eA2 = +
Selective region for A Selective region for A
k A B eA eB At each non-selective wavelength A = eA [A] + eB [B] = eA eB = +
k A B eA eA eA eA eA eA eB eB eB eB eB eB At each non-selective region = C = f(k) A = C ET + R R = A – C C+ A R = f(k)
? Is there any limitation in numbers of wavelengths?
? How one can find the error of calculated parameter?