2014/01/01 by Hervé Cottet, Jean-Philippe Biron, Jean‐Philippe Biron +1 · 6 citations
Chemistry · Engineering · #Analytical Chemistry (journal) #Capillary action #Chemistry #Chromatography #Composite material #Computer science #Dispersion (optics) #Heat and Mass Transfer in Porous Media #Innovative Microfluidic and Catalytic Techniques Innovation #Materials science #Mechanics #Microfluidic and Capillary Electrophoresis Applications #Optics #Physics #RADIUS #Taylor dispersion #Thermodynamics #Work (physics)
paper · doi:10.1039/c4an00192c
openalex publication_date 2014/01/01 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/26
In this work, we investigate the possibility of optimizing the operating conditions, namely mobilizing pressure, capillary length and capillary radius, for performing Taylor dispersion analysis on solutes having hydrodynamic diameter, 2Rh, between 1 and 100 nm. Optimizing Taylor dispersion analysis means finding the set of operating conditions that verify the conditions of validity of this method, and finding the most appropriate conditions that may enhance or maximize the separation performances. Our conclusion is that the performances of Taylor dispersion analysis are independent of the operating conditions, as far as the conditions of validity of the method are verified. The inequalities defining the set of acceptable operating conditions are given in this work as a function of the maximal relative error on the diffusion coefficient, D, fixed by the user. These inequalities define operating zones that were represented for three typical capillary diameters (25, 50 and 100 μm). Within these zones, all experiments should lead to similar results on D (or Rh) and similar separation performances. It was concluded that assuming a 3% relative error on the determination of D, a 60 cm × 50 μm i.d. capillary can be used by default for performing TDA of analytes in the 1-100 nm diameter range with mobilizing pressure in the 50-100 mbar range.