Impacts of sulfur source and temperature on sulfur-driven denitrification by pure and mixed cultures of Thiobacillus

反硝化 硫代硫酸盐 硫黄 硫杆菌 化学 无机化学 硝酸盐 核化学 氮气 环境化学 有机化学
作者
Francesco Di Capua,Sarita Ahoranta,Stefano Papirio,Piet N.L. Lens,Giovanni Esposito
出处
期刊:Process Biochemistry [Elsevier BV]
卷期号:51 (10): 1576-1584 被引量:165
标识
DOI:10.1016/j.procbio.2016.06.010
摘要

This study investigated the impacts of thiosulfate (S2O32−) as well as chemically synthesized and biogenic elemental sulfur (S0) on the rates of sulfur-based denitrification in batch bioassays. The use of S2O32− resulted in the highest denitrification rate (52.5 mg N-NO3−/L d), whereas up to 10 times slower nitrate (NO3−) removal was observed with S0. Biogenic S0 was tested for the first time as electron donor for chemolithotrophic denitrification, resulting in 1.7-fold faster NO3− removal than that achieved with chemically synthesized S0. The effects of increasing concentrations of S2O32− and chemically synthesized S0 on denitrification were evaluated testing three different sulfur-to-nitrogen (S/N) molar ratios (1.8, 3.5 and 5.1) on a pure culture of Thiobacillus denitrificans and a mixotrophic enrichment dominated by Thiobacillus thioparus. S2O32− concentrations exceeding 2.2 g/L inhibited the activity of T. denitrificans, whereas a stimulatory effect was observed on mixotrophic denitrification. The increase in S0 concentration slightly enhanced denitrification by both microbial cultures due to the low solubility of chemically synthesized S0. The temperature dependence of the thiosulfate-driven denitrification by T. denitrificans was investigated to further optimize the process and modeled by the Arrhenius equation with an apparent activation energy Ea of 76.6 kJ/mol and a temperature coefficient Q10 of 3.0.
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