Exploring nutrient removal mechanisms in column-type SBR with simultaneous nitrification and denitrification

Abstract

A comprehensive investigation utilized a column-type sequencing batch reactor (SBR) to efficiently remove nutrients throughout various phases of its operational cycle by forming granules. This study assessed the influence and mechanisms of a simultaneous nitrification and denitrification (SND) system employing a column-type sequential batch reactor (SBR). The primary focus was on elucidating the functional groups involved in nitrogen transformation and removal within the extracellular polymeric substances (EPS). The research findings demonstrate the superior performance of the SBR process compared to the control group. It achieved an impressive SND efficiency of 69%, resulting in a remarkable 66% total nitrogen removal. Furthermore, a detailed analysis unveiled that the SBR process had a beneficial impact on the composition and properties of EPS. This impact was observed through increased EPS content and enhanced capacity to transport, convert, and retain nitrogen effectively. Additionally, after initial acclimatization, the SBR process showed its effectiveness in removing nutrients (88–98%) and COD (93%) from the generated wastewater within a hydraulic retention time (HRT) of 6 h. A statistically significant difference between the treatments for the investigated mixing ratios was found by univariate analysis of variance (ANOVA). Machine learning (CatBoost model) was employed to understand each parameter’s relationship and predict the outcomes in measurable quantity. The findings of the SBR trials showed that the concentration of generated wastewater and the HRT impacted the treatment efficiency. However, the effluent may still need other physicochemical processes, such as membrane filtering, coagulation, electrocoagulation, etc., as post-treatment options, even though COD, nutrients, and turbidity have been entirely or significantly effectively removed. Overall, this work offers insightful information on the critical function of the SBR bacterial community in promoting SND.