The anion impurities such as SO42-, Cl-, and Cr2O72- commonly present in the spent (hazardous) Cr-etch solutions from color filter manufacturing processes may influence the solutions' regeneration by the electrooxidation of Ce(III) to Ce(IV). This study, therefore, investigated the effects of these anions on Ce(III)/Ce(IV) redox reactions at glassy carbon in HNO3 - In cyclic voltammetric tests, the presence of SO42- decreased the formal potential but increased the peak potential separation (Delta E-p) of Ce(III)/Ce(IV) couple, and lowered the peak current for Ce(IV) reduction whereas Cl- did not change the formal potential and Delta E-p but the peaks for Cl- and Ce(III) oxidation partially overlapped. Cr2O72- slightly lowered the peak current for Ce(III) oxidation but significantly decreased that for Ce(IV) reduction. The Tafel slope for Ce(III) oxidation was similar to 65 mV decade(-1) the absence of anion impurities. Increasing SO42-, Cl-, or Cr2O72- in solution raised the Tafel slope. The Ce(III)/Cc(IV) equilibrium potential decreased with the increase Of SO42- or Cl- but was hardly influenced by Cr2O72- addition. These observations from individual anion species together well explained the anions' co-effect (kinetic hindrance) on the Ce(III) oxidation in HNO3, revealing that these anions are unfavorable for the electrooxidation of Ce(III) in the spent Cr-etch solutions. (C) 2007 Elsevier B.V. All rights reserved.