posted on 2016-05-02, 00:00authored byD.K. Hubler, J.C. Baygents, B.P. Chaplin, J. Farrell
This research investigated reaction pathways for formation of chlorite and chlorate when using boron doped diamond (BDD) film
anodes for generating hypochlorite. Batch electrolysis and voltammetry experiments were performed to investigate the rates and
potential dependency of hypochlorite and chlorite oxidation. Density functional theory (DFT) modeling was used to investigate
possible reaction pathways. The DFT simulations included reactions with hydrogen terminated surfaces, and with surface sites
produced by anodic polarization, namely: ≡C•, =C•H, ≡C–O• and =C•HO. Oxychlorine radicals (ClO•, ClO2
•) were found to
chemically adsorb to both secondary and tertiary carbon atoms on the BDD surface. These chemisorbed intermediates could react
with hydroxyl radicals to regenerate the original chlorine oxyanion (ClO− or ClO2
−), and produce ≡C–O• and =C•HO sites on
the BDD surface. The ≡C–O• and =C•HO sites also reacted with oxychlorine radicals to form chemisorbed intermediates, which
could then be converted to higher oxidation states (ClO2
−, ClO3
−) via reaction with hydroxyl radicals. The predominant pathway
for chlorite and chlorate production appears to involve oxidation of HOCl or HClO2 via direct electron transfer, followed by reaction
of ClO• or ClO2
• with a hydroxyl radical.
Funding
Funding for this work was provided by the National Science Foundation
(CBET-0931749).