AI Article Synopsis

  • The sulfur-based denitrification process is gaining attention because it eliminates the need for added organics and minimizes risks related to chemical oxygen demand (COD).
  • The proposed SICAD system, which combines sulfur with iron(II) carbonate ore, improves denitrification by acting as a buffer and electron donor while effectively extending the reaction area for bacteria.
  • The SICAD system significantly outperforms traditional methods, achieving higher denitrification rates and reduced intermediate accumulation, suggesting its potential as a highly efficient post-denitrification solution.

Article Abstract

Sulfur-based denitrification process has attracted increasing attentions because it does not rely on the external addition of organics and avoids the risk of COD exceeding the limit. Traditionally, limestone is commonly employed to maintain a neutral condition (SLAD process), but it may reduce the efficiency as the occupied zone by limestone cannot directly contribute to the denitrification. In this study, we propose a novel sulfur-based denitrification process by coupling with iron(II) carbonate ore (SICAD system). The ore was demonstrated to play roles as the buffer agent and additional electron donor. Moreover, the acid produced through sulfur driven denitrification was found to promote the Fe(II) leaching from the ore and likely extend the reaction zone from the surface to the liquid. As a result, more biomass was accumulated in the SICAD system compared with the controls (sulfur, iron(II) carbonate ore and SLAD systems). Owing to these synergistic effects of sulfur and iron(II) carbonate on denitrification, SICAD system showed much higher denitrification rate (up to 720.35 g·N/m·d) and less accumulation of intermediates (NO and NO) than the controls. Additionally, sulfate production in SICAD system was reduced. These findings offer great potential of SICAD system for practical use as a highly efficient postdenitrification process.

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Source
http://dx.doi.org/10.1021/acs.est.8b06865DOI Listing

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