Abstract

Weak base phenol formaldehyde anion exchange resins were found to have an excellent capacity for removing the anionic organic species benzenesulfonate (BS), p-toluenesulfonate (PTS) and dodecylbenzenesulfonate (DBS) from pH 2 and 4 solutions. The capacity for DBS was generally greater than that of activated carbon and significantly greater than that of a polystyrene-divinylbenzene resin with no ion exchange functional groups. The maximum capacity of the weak base resins appeared to be limited by the exchange capacity of the resin. The mechanism of removal was strongly indicated as being either ion exchange at the amine functional groups in the acid form, or uptake of a proton by the amine groups in the free base form with the organic anion as the associated counter ion. Increasing concentrations of Cl− decreased the amount of organic anion that could be sorbed.The swelling of one of the resins, Duolite A-7, also had a marked effect on its sorption capacity. The pores of the acid chloride or acid organic anion form of the resin were apparently larger than those of the free base form; thus, as conversion of the resin to the acid form took place, a greater amount of uptake was observed. The effect of swelling on the capacity of Duolite S-37 was much less, apparently owing to its larger pore structure, but its capacity for DBS at low pH was lower than that for A-7 because of its lower nitrogen content. Also, BS and DBS were easily removed from the weak base resins by washing them with NaOH. Four bed volumes of 1 m NaOH gave essentially complete regeneration of BS saturated A-7.

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