Evaluating the Feasibility of Two Reduced Sulfur Compounds as Energy Sources and Electron Donors for Partial Autotrophic Denitrification: Thiocyanate and Sulfite

Autotrophic denitrification using sulfur compounds is considered an alternative to heterotrophic denitrification for the treatment of organic carbon-deficient wastewaters. However, the stoichiometric characteristics of denitrification using different sulfur species, particularly thiocyanate (SCN−) and sulfite (SO32−), remain poorly understood. Here, partial autotrophic denitrification driven by thiocyanate or sulfite was studied in two batch reactors. The stoichiometry of thiocyanate-oxidizing denitrification was assessed based on valence and ultimate product analysis. No nitrate removal was observed in the sulfite-fed system, indicating that sulfite could not serve as an effective electron donor for autotrophic denitrification under the tested conditions. In contrast, simultaneous removal of SCN− and NO3− was achieved in the thiocyanate-fed system, with removal efficiencies of 100% and 92.5 ± 3.6%, respectively. After 36 h, total nitrogen removal reached 63.3%, with nitrite identified as the dominant intermediate product (26.7%). NO2− and NH4+ accumulated during the process could be further removed through anaerobic ammonium oxidation. Thiocyanate sulfur was primarily oxidized to sulfate via elemental sulfur as a transient intermediate. These findings provide a theoretical basis for applying thiocyanate-driven partial autotrophic denitrification to nitrogen removal from industrial wastewaters, particularly those generated via coal gasification and cyanide-utilizing gold mining processes.