Diverse mathematical models for chromatographic peak description-Gaussian, log-normal, gamma, Weibull, Haarhoff and der Van Linde, Littlewood, exponentially modified Gaussian, Gram-Charlier, and Edgeworth-Cramer series-are evaluated by curve fitting to solutions of the differential mass balance equation obtained numerically by an implicit finite differences method. The peak profiles generated from this equation are representative of diverse integration conditions encompassing different adsorption equilibrium isotherms (linear, Langmuir, and Freundlich), injection modes (pulse, exponential, reverse ramp, semiparabolic, and triangular), and axial longitudinal dispersion coefficients. Curve fitting is performed with a generalized least-squares method. The results show a good correspondence between the solutions of the mass balance equation, combined with a linear isotherm, and symmetric injection modes, with the Gaussian function and the functions that may approach Gaussian expressions (exponentially modified Gaussian, Gram-Charlier, Edgeworth-Cramer, log-normal, Haarhoff and der Van Linde). The exponentially modified Gaussian function gives the best fit for the profiles generated with this isotherm and the exponential injection modes. The solution of the mass balance equation, combined with the Langmuir isotherm, shows that the Haarhoff and der Van Linde function is better adapted to this type of profile. Finally, a good correlation between the log-normal function and the solutions of the mass balance equation, combined with the Freundlich isotherm, is observed
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