1. Effect of the presence of inorganic ions and operational parameters on free cyanide degradation by ultraviolet C activation of persulfate in synthetic mining wastewater
- Author
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Efraím A. Serna-Galvis, Valentina Satizabal-Gómez, Samir Fernando Castilla-Acevedo, Manuel Alejandro Collazos-Botero, Ricardo A. Torres-Palma, Juan J. Bravo-Suárez, and Fiderman Machuca-Martínez
- Subjects
Cyanide ,Inorganic chemistry ,Inorganic ions ,chemistry.chemical_element ,Persulfate ,02 engineering and technology ,010501 environmental sciences ,Advanced oxidation process ,01 natural sciences ,Oxygen ,020501 mining & metallurgy ,chemistry.chemical_compound ,Free cyanide degradation ,Dissolved oxygen ,Reaction rate constant ,Nitrate ,Mining wastewater ,0105 earth and related environmental sciences ,Mechanical Engineering ,General Chemistry ,Geotechnical Engineering and Engineering Geology ,Phosphate ,0205 materials engineering ,chemistry ,Control and Systems Engineering - Abstract
This work studied the influence of several parameters on free cyanide (CN−) degradation (50 mg L−1) by the UVC-activated persulfate (PS) at alkaline conditions (UVC/PS). Firstly, photolysis and alkaline activation of PS were evaluated. Then, the effect of initial PS concentration (0.2, 0.4, and 0.6 g L−1) and dissolved oxygen in solution (absence/presence) were studied. Lastly, the influence of phosphate, carbonate, and nitrate presence at different concentrations (50, 150, 350, and 500 mg L−1) on CN− elimination was tested. Additionally, the electric energy per order (EEO), a measure of the energy consumption in the process was determined, and a mechanistic view of CN− degradation was proposed. The results show that photolysis and alkaline activation of PS degraded 8 and 11% of CN−, respectively, whereas their combination presented a synergistic effect on CN− pollutant elimination. While oxygen had a vital role in photolysis due to the formation of 1O2 to oxidize CN− to CNO−, HO• and SO4•− were primarily responsible for CN− degradation by UVC/PS. It was also found that cyanide removal followed a pseudo-first-order kinetics whose apparent reaction rate constant (k) increased from 0.0104 to 0.0297 min−1 as the initial concentration of PS increased from 0.2 to 0.6 g L−1, indicating a strong dependency of the removal efficiency on the PS amount. Remarkably, cyanide degradation by the combined UVC/PS showed a high CN− conversion and selectivity even in the presence of high concentrations of phosphate, carbonate, and nitrate ions (500 mg L−1), which resulted in CN− removals higher than 80% after 60 min of degradation treatment. Furthermore, the EEO values were similar in the presence and absence of phosphate or carbonate; however, they decreased slightly with nitrate presence. All these results suggest the feasibility of the combined UVC/PS process for the elimination of cyanide such as that found in mining wastewater.
- Published
- 2021