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Resolution is calculated using the separation of two peaks in terms of their average peak width at the base (tR2 > tR1). In the case of two adjacent peaks, it may be assumed that the peak width at the base wb1 wb2, and thus, the width of the second peak may be substituted for the average value.
Resolution is calculated using the separation of two peaks in terms of their average peak width at the base (tR2 > tR1). In the case of two adjacent peaks, it may be assumed that the peak width at the base wb1 wb2, and thus, the width of the second peak may be substituted for the average value.
Equation (1) indicates that the resolution is the difference between peak retention times divided by the average peak width. In a peak with Gaussian distribution, the peak width is W = 4 (where is the standard deviation) and the peak FHM is W0.
In chromatography, resolution is a measure of the separation of two peaks of different retention time t in a chromatogram.
One of the simplest ways to improve resolution is to adjust solute B's retention factor. If all other terms in equation 12.19 remain constant, increasing KB improves resolution. As shown by the green curve in Figure 12.15, however, the improvement is greatest if the initial value of KB is small.
It is generally calculated by k' = (tR — TM)/TM = tRy'/TM. g) The selectivity factor () of a column for two analytes (A eluting before B) is given by = KB/A = k'(B)/k'(A) = tRy'(B)/tR'(A).
Resolution. The resolution of an elation is a quantitative measure of how well two elation peaks can be differentiated in a chromatographic separation. It is defined as the difference in retention times between the two peaks, divided by the combined widths of the elation peaks.
Resolution (r) = 1.22/(NA(obj) + NA(cold)) Where r is resolution (the smallest resolvable distance between two objects), NA is a general term for the microscope numerical aperture, is the imaging wavelength, NA(obj) equals the objective numerical aperture, and NA(cold) is the condenser numerical aperture.
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