Divalent/Monovalent Selectivities and Secondary Interactions of Multibasic Acids on Anion Exchange Resins

Abstract

The ion exchange equilibria of Br<sup>–</sup> on three strongly basic anion exchange resins of different exchange capacities and different cross-linking degrees by five alkanoates (MC<sub><i>m</i></sub>), a phosphate, and eight alkanedioates (DC<sub><i>n</i></sub>; <i>m</i>,<i>n</i> = number of carbon atoms) were analyzed, and the selectivity coefficients for their monoanion and dianion, <i>K</i><sub>11</sub> and <i>K</i><sub>21</sub> were evaluated as a function of percent exchange (%E). The decrease in the <i>K</i><sub>11</sub> values of MC<sub><i>m</i></sub> with an increase in %E was attributed to the interference with hydration of MC<sub><i>m</i></sub> in the resin phase, while the increase in the <i>K</i><sub>11</sub> values of DC<sub><i>n</i></sub> to the intermolecular hydrogen bonding between exchanged acidic anions. The log <i>K</i><sub>21</sub> values of DC<sub><i>n</i></sub> at %<i>E</i> = 0 plotted against <i>n</i> showed the minimum rather than the maximum as described previously. The reason has been discussed in terms of the hydrophobic interaction of DC<sub><i>n</i></sub> with the polymer matrix, intramolecular hydrogen bonding, and the charge density

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