Solvent Effect upon Ion-pair Extraction of Different Sodium Dyes Using Some Crown Ethers

Liquid-liquid extractive-spectrophotometric studies of sodium ion complexes of 18-crown-6(18C6), dibenzo-18-crown-6(DB18C6), 15-crown-5(15C5), and 12-crown-4(12C4) and anionic dyes 4-(2-pyridylazo)-resorcinol monosodium salt monohydrate (PAR), Eriochrom Black T (EBT), and methyl orange (MOR)] and sodium picrate (PICRAT) as the counter ion are described. The overall extraction equilibrium constants for the 1 : 1 complexes of the above crown ethers with sodium dyes between different organic solvents and water have been determined at 25deg;C. They were conducted in various solvent-water systems maintaining an identical initial cation concentration in water, M0+]w, and macrocyclic ligand concentration in the organic phase, L0]org}, so that in all extractions M0+]w : L0]org ratios were 1 : 1, 1 : 10, 1 : 20, 1 : 50, and 1 : 62.5. An ion association complex formed between the sodium-crown ether complex ion and a dye anion was extracted into the organic solvent, and then the dye concentration of the separated aqueous phase was measured with an ultraviolet-visible spectrophotometer. PAR was the best associated dye with all crown ethers sodium-dyes and the extracted dye occurs as the ion-pair complex. Methylene chloride was found to be better than other extractive solvents used in this study.