RESUMEN
Sulfur autotrophic denitrification (SAD) process, as an alternative to heterotrophic denitrification (HD) filter, receives growing interest in polishing the effluent from secondary sewage treatment. Although individual studies have indicated several advantages of SAD over HD, rare study has compared these two systems under identical condition and by using real secondary effluent. In this study, two small pilot scale filters (SAD and HD) were designed with identical configuration and operated parallelly by feeding the real secondary effluent from a WWTP. The results showed SAD filter can be started up without the addition of soluble electron donor, although the time (14 days) was about 3 times longer than that of HD filter. The nitrate removal rate of SAD filter at HRT of 1.4 h was measured as 0.268 ± 0.047 kg N/(m3âd). Similar value was observed in HD filter with supplementing 90 mg/L COD. The COD concentration of effluent always kept lower than that of influent in SAD filter but not in HD filter. In addition, SAD filter could maintain a stable denitrification performance without backwash for 15 days, while decline of nitrate removal rate was observed in HD filter just 2 days after stopping the backwash. This different behavior was further confirmed as the SAD filter had a better hydraulic flow pattern. Analysis according to high-throughput 16S rRNA gene-based Illumina MiSeq sequencing clearly showed the microbial community evolution and differentiation among the samples of seed sludge, SAD and HD filters. Finally, the economic assessment was carried out, showing the operation cost of SAD filter was over 50% lower than that of HD filter.
Asunto(s)
Desnitrificación , Hidrodinámica , Reactores Biológicos , Nitratos , Nitrógeno , ARN Ribosómico 16S/genética , AzufreRESUMEN
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/m3·d) and less accumulation of intermediates (NO2- and N2O) 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.
Asunto(s)
Desnitrificación , Compuestos Ferrosos , Procesos Autotróficos , Reactores Biológicos , Hierro , Nitratos , AzufreRESUMEN
Biological removal of nitrate, a highly concerning contaminant, is limited when the aqueous environment lacks bioavailable electron donors. In this study, we demonstrated, for the first time, that bacteria can directly use the electrons originated from the photoelectrochemical process to carry out the denitrification. In such photoelectrotrophic denitrification (PEDeN) systems (denitrification biocathode coupling with TiO2 photoanode), nitrogen removal was verified solely relying on the illumination dosing without consuming additional chemical reductant or electric power. Under the UV illumination (30 mW·cm-2, wavelength at 380 ± 20 nm), nitrate reduction in PEDeN apparently followed the first-order kinetics with a constant of 0.13 ± 0.023 h-1. Nitrate was found to be almost completely converted to nitrogen gas at the end of batch test. Compared to the electrotrophic denitrification systems driven by organics (OEDeN, biocathode/acetate consuming bioanode) or electricity (EEDeN, biocathode/abiotic anode), the denitrification rate in PEDeN equaled that in OEDeN with a COD/N ratio of 9.0 or that in EEDeN with an applied voltage at 2.0 V. This study provides a sustainable technical approach for eliminating nitrate from water. PEDeN as a novel microbial metabolism may shed further light onto the role of sunlight played in the nitrogen cycling in certain semiconductive and conductive minerals-enriched aqueous environment.
Asunto(s)
Desnitrificación , Nitratos , Reactores Biológicos , Electricidad , Nitrógeno , Óxidos de NitrógenoRESUMEN
In this study, a novel scaled-up hybrid acidogenic bioreactor (HAB) was designed and adopted to evaluate the performance of azo dye (acid red G, ARG) containing wastewater treatment. Principally, HAB is an acidogenic bioreactor coupled with a biocatalyzed electrolysis module. The effects of hydraulic retention time (HRT) and ARG loading rate on the performance of HAB were investigated. In addition, the influent was switched from synthetic wastewater to domestic wastewater to examine the key parameters for the application of HAB. The results showed that the introduction of the biocatalyzed electrolysis module could enhance anoxic decolorization and COD (chemical oxygen demand) removal. The combined process of HAB-CASS presented superior performance compared to a control system without biocatalyzed electrolysis (AB-CASS). When the influent was switched to domestic wastewater, with an environment having more balanced nutrients and diverse organic matters, the ARG, COD and nitrogen removal efficiencies of HAB-CASS were further improved, reaching 73.3%±2.5%, 86.2%±3.8% and 93.5%±1.6% at HRT of 6 hr, respectively, which were much higher than those of AB-CASS (61.1%±4.7%, 75.4%±5.0% and 82.1%±2.1%, respectively). Moreover, larger TCV/TV (total cathode volume/total volume) for HAB led to higher current and ARG removal. The ARG removal efficiency and current at TCV/TV of 0.15 were 39.2%±3.7% and 28.30±1.48 mA, respectively. They were significantly increased to 62.1%±2.0% and 34.55±0.83 mA at TCV/TV of 0.25. These results show that HAB system could be used to effectively treat real wastewater.
Asunto(s)
Compuestos Azo/aislamiento & purificación , Compuestos Azo/metabolismo , Biocatálisis , Reactores Biológicos , Electrólisis/instrumentación , Eliminación de Residuos Líquidos/métodos , Aguas Residuales/química , Aerobiosis , Biodegradación Ambiental , Análisis de la Demanda Biológica de Oxígeno , Colorantes/aislamiento & purificación , Colorantes/metabolismo , Electrodos , Concentración de Iones de Hidrógeno , Eliminación de Residuos Líquidos/instrumentación , Contaminantes Químicos del Agua/aislamiento & purificación , Contaminantes Químicos del Agua/metabolismoRESUMEN
Nitrate is one of the most common pollutants in the water environment. A key factor for the effective control and removal of nitrate is the ability to accurately determine the nitrate concentration in groundwater and the secondary effluent of wastewater treatment plants. Here, a bioelectrochemical method for real-time detection of the nitrate was developed. In this work, a kinetic model was developed to describe the correlation between the nitrate concentration and the current. Standard addition experiments showed the relative error between indicator predictions and ion chromatographic values ranged from 3.14% to 9.74%. The monitoring results of secondary effluent showed that the system could give a good response at different nitrate concentrations. The average error of not >10.85% between the indicator predictions and ion chromatographic values was demonstrated. This study offers a new method for the development of sustainable bioelectrochemical system (BES)-based technology for the real-time detection of nitrate in groundwater and the secondary effluent.
Asunto(s)
Técnicas Electroquímicas/métodos , Monitoreo del Ambiente/métodos , Agua Subterránea/análisis , Nitratos/análisis , Contaminantes Químicos del Agua/análisis , Técnicas Electroquímicas/instrumentación , Monitoreo del Ambiente/instrumentación , Diseño de Equipo , Cinética , Aguas Residuales/análisisRESUMEN
A bioelectrochemical system (BES) is a technology with potential for accelerating the degradation of recalcitrant compounds, the components and configurations of which are important for treatment performance. In the present work, a membraneless sleeve-type BES (termed BioE) was designed for the treatment of synthetic coal gasification wastewater (CGW, phenol as a model pollutant) and real CGW. Compared with the biological control (termed Bio), the phenol removal rate and COD removal efficiency increased by 2.6 and 2.1 fold in the BioE, respectively. However, the coulombic efficiency of this system was relatively low, ranging from 0.42% to 2.6%. This combination of results indicated that anode respiration was not the main process in the BioE. The increased CH4 production and higher levels of methanogens obtained from the BioE confirmed that the methanogenic process proceeded, possibly facilitated by the diffusion of H2 from the cathode to the anode. This study provides new insight into biocathode function for COD oxidation removal in BESs. Moreover, this study indicates that pursuing a high coulombic efficiency may not be necessary for wastewater treatment, as it consumes less energy at the lower value.
Asunto(s)
Reactores Biológicos/microbiología , Carbón Mineral/análisis , Fenoles/aislamiento & purificación , Eliminación de Residuos Líquidos/instrumentación , Aguas Residuales/análisis , Contaminantes Químicos del Agua/aislamiento & purificación , Análisis de la Demanda Biológica de Oxígeno , Electrodos , Diseño de EquipoRESUMEN
The Nernst-Monod model is used to describe bio-anode performance with respect to the effect of the electron donor and anode potential. However, electron competition is not considered in the model, limiting its application in wastewater treatment systems. In this work, nitrate was employed to describe the influence of a competitive electron acceptor on bio-anode performance. A new dynamic model of microbial anode respiration and nitrate respiration was developed for the removal of nitrogen oxides. The competitive relationship between microbial anode respiration and nitrate respiration was investigated based on electron transfer as described by the kinetics of Nernst-Monod electron transfer and nitrate reduction. The experimental results showed that nitrate had a significant influence on microbial anode respiration. The model parameters were estimated with the experimental results obtained in a continuous-flow bioelectrochemical system (BES) fed with acetate. The simulated results revealed that nitrate respiration could indirectly affect the microbial anode respiration by altering the available substrate concentration. In addition, bacterial community analysis indicated that there were two dominant functional microorganisms coexisting in the anode chamber. The first microorganism was represented by Geobacter, which has extracellular electron-transfer abilities. The second was denitrifying bacteria, which can use the carbon sources in the anodic chamber and electrons from the electrode for nitrate reduction. This is the first time that mathematical modelling of nitrate reduction has been applied to BESs.
Asunto(s)
Fuentes de Energía Bioeléctrica/microbiología , Geobacter/metabolismo , Nitratos/metabolismo , Aguas Residuales/microbiología , Electricidad , Electrodos , Transporte de Electrón , Diseño de Equipo , Cinética , Modelos Biológicos , Nitratos/aislamiento & purificación , Purificación del AguaRESUMEN
The application of bio-electrochemical system (BESs) is strongly depended on the development of the engineering applicable electrode. Here we described an economical and readily processable electrode module with three-dimensional structure, the corrugated stainless-steel mesh electrode module (c-SMEM). This novel developed electrode module was demonstrated to provide a good hydrodynamic characteristic and significantly enhanced the decolorization performance of the BES when serving for treating azo dye (acid orange 7, AO7) containing wastewater. Compared to the conventional planar electrodes module (p-SMEM), c-SMEM was found to prolong the mean residence time (MRTθ) of AO7 and change the flow pattern closer to the plug flow. As a result, the maximum enhancement of the volumetric decolorization rate (vDR) can reach to 255%, even when the c-SMEM and p-SMEM have the same electrode surface area. In addition, a techno-economic analysis model was established to elucidated the effects of the decolorization performance and the material cost on the initial capital cost, which revealed the BES with c-SMEM could be economically comparable to or even better than the traditional bio-decolorization technologies. These results suggest c-SMEM holds great potential for engineering application, which may help paving the way of applying BES at large-scale.