Mass-Transfer Simulation of Salicylic Acid on Weakly Polar Hyper-cross-linked Resin XDA-200 with Coadsorption of Sodium Ion.

The mass-transfer process of salicylic acid on hyper-cross-linked resin XDA-200 was experimentally and theoretically studied. Undissociated salicylic acid was found to be the favorable form for salicylic acid adsorption on the resin. A pH-dependent adsorption isotherm model established in this paper could well fit the adsorption isotherm data at different pH values. Surface diffusion is the main mass-transfer mode for salicylic acid in resin particles. The salicylate anions and Na+ coadsorbed on the resin. The modified surface diffusion model considering the coadsorption was proposed. The model could satisfactorily fit the concentration decay curves of salicylic acid at different pH values and feed concentrations. NaOH aqueous solution at pH 12 could elute salicylic acid in the fixed bed efficiently. A pH-dependent dynamic adsorption and elution process model considering axial diffusion, external mass transfer, surface diffusion, pH-dependent adsorption equilibrium, as well as coadsorption of salicylate anions and Na+ was established. The model could well predict the breakthrough and elution curves at different feed concentrations. The research carried out in this paper has reference significance for optimizing the separation process of salicylic acid and its analogues.

Adsorption separation of guanosine 5'-Monophosphate and cytidine 5'-Monophosphate by mixed-mode Resin HD-1: Experimental study and mathematical modeling.

The preparative separation of guanosine 5'-monophosphate (GMP) and cytidine 5'-monophosphate (CMP) on mixed-mode resin HD-1 was experimentally and theoretically investigated. The adsorption mechanisms of the two nucleotides were elucidated by analyzing adsorption equilibria and kinetics at different pH values. The adsorption dynamics of GMP and CMP in a fixed bed packed with resin HD-1 were studied. All nucleotide monovalent cations, zwitterions, and monovalent anions were adsorbed by the resin. Further, a general adsorption isotherm model was developed by considering the adsorption of different nucleotide species and the dissociation equilibrium behaviors of resin ligands. The model fit the adsorption isotherm data of GMP and CMP well. A modified liquid-film linear driving force model with the combined physical adsorption of nucleotides in different dissociation states and ion exchange of Na+ was established. The dissociation equilibria of resin ligands and nucleotides were considered. The model satisfactorily predicted the adsorption kinetic data at different pH values. The values of the efficient diffusion coefficients for GMP and CMP were not significantly influenced by the solution pH. A modified transport-diffusion model with pH gradient elution was proposed. The model accurately predicted the elution chromatographic peaks of GMP and CMP, as well as the pH at the outlet of the fixed bed packed with resin HD-1.