Van Deemter equation

The Van Deemter equation in chromatography relates the variance per unit length of a separation column to the linear mobile phase velocity by considering physical, kinetic, and thermodynamic properties of a separation.[1] These properties include pathways within the column, diffusion (axial and longitudinal), and mass transfer kinetics between stationary and mobile phases. In liquid chromatography, the mobile phase velocity is taken as the exit velocity, that is, the ratio of the flow rate in ml/second to the cross-sectional area of the ‘column-exit flow path.’ For a packed column, the cross-sectional area of the column exit flow path is usually taken as 0.6 times the cross-sectional area of the column. Alternatively, the linear velocity can be taken as the ratio of the column length to the dead time. If the mobile phase is a gas, then the pressure correction must be applied. The variance per unit length of the column is taken as the ratio of the column length to the column efficiency in theoretical plates. The Van Deemter equation is a hyperbolic function that predicts that there is an optimum velocity at which there will be the minimum variance per unit column length and, thence, a maximum efficiency. The Van Deemter equation was the result of the first application of rate theory to the chromatography elution process.

Van Deemter equation

The van Deemter equation relates the resolving power (HETP, height equivalent to a theoretical plate) of a chromatographic column to the various flow and kinetic parameters which cause peak broadening, as follows:

HETP = A + \frac{B}{u} + (C_s +C_m)\cdot u

Where

In open tubular capillaries, the A term will be zero as the lack of packing means channeling does not occur. In packed columns, however, multiple distinct routes ("channels") exist through the column packing, which results in band spreading. In the latter case, A will not be zero.

The form of the van Deemter equation is such that HETP achieves a minimum value at a particular flow velocity. At this flow rate, the resolving power of the column is maximized, although in practice, the elution time is likely to be impractical. Differentiating the van Deemter equation with respect to velocity, setting the resulting expression equal to zero, and solving for the optimum velocity yields the following:

u = \sqrt{\frac{B}{C}}

Plate count

Two well resolved peaks in a chromatogram

The plate height given as:

H = \frac{L}{N} \,

with L \, the column length and :N\, the number of theoretical plates can be estimated from a chromatogram by analysis of the retention time t_R \, for each component and its standard deviation \sigma \, as a measure for peak width, provided that the elution curve represents a Gaussian curve.

In this case the plate count is given by:[2]

N = \left(\frac{t_R}{\sigma}\right)^2 \,

By using the more practical peak width at half height W_{1/2} \, the equation is:

N = 8 \ln(2) \cdot \left(\frac{t_R}{W_{1/2}}\right)^2 \,

or with the width at the base of the peak:

N = 16 \cdot \left(\frac{t_R}{W_{base}}\right)^2 \,

Expanded van Deemter

The Van Deemter equation can be further expanded to:[3]

H = 2\lambda d_p + {2\gamma D_m \over u} + {\omega(d_p \mbox{ or } d_c)^2 u \over D_m}+{Rd_f^2 u \over D_s}

Where:

External links

See also

Rodrigues equation

References

  1. ↑ van Deemter JJ, Zuiderweg FJ and Klinkenberg A (1956). "Longitudinal diffusion and resistance to mass transfer as causes of non ideality in chromatography". Chem. Eng. Sc. 5: 271–289. doi:10.1016/0009-2509(56)80003-1.
  2. ↑ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (2006–) "plate number, N".
  3. ↑ Kazakevich, Yuri. "Band broadening theory (Van Deemter equation)". Seton Hall University. Retrieved 5 February 2014.
This article is issued from Wikipedia - version of the Thursday, November 26, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.