Xueqin Lu

Enhanced dewaterability of sewage sludge in the presence of Fe(II)-activated persulfate oxidation

The potential benefits of Fe(II)-activated persulfate oxidation on sludge dewatering and its mechanisms were investigated in this study. Capillary suction time (CST) was used to evaluate sludge dewaterability. Both extracellular polymeric substances (EPS) and viscosity were determined in an attempt to explain the observed changes in sludge dewaterability. The optimal conditions to give preferable dewaterability characteristics were found to be persulfate (S(2)O(8)(2-)) 1.2 mmol/gVSS, Fe(II) 1.5 mmol/gVSS, and pH 3.0-8.5, which demonstrated a very high CST reduction efficiency (88.8% reduction within 1 min). It was further observed that both soluble EPS and viscosity played relatively negative roles in sludge dewatering, whereas no correlation was established between sludge dewaterability and bound EPS. Three-dimensional excitation-emission matrix (EEM) fluorescence spectra also revealed that soluble EPS of sludge were degraded and sludge flocs were ruptured by persulfate oxidation, which caused the release of water in the intracellular pace and subsequent improvement of its dewaterability.

Novel insights into enhanced dewaterability of waste activated sludge by Fe(II)-activated persulfate oxidation

The potential of Fe(II)-activated persulfate (S(2)O(8)(2-)) oxidation on enhancing the dewaterability of sludge flocs from 3-full scale wastewater treatment plants (WWTPs) were investigated. Normalized capillary suction time (CST) was applied to evaluate sludge dewaterability. Both extracellular polymeric substances (EPS) and metabolic activity of microorganisms were determined to explore the responsible mechanism. Fe(II)-S(2)O(8)(2-) oxidation effectively improved sludge dewaterability. The most important mechanisms were proposed to be the degradation of EPS incorporated in sludge flocs and rupture of microbial cells. Three-dimensional excitation-emission matrix (EEM) fluorescence spectroscopy confirmed that the powerful SO(4)(-) from Fe(II)-S(2)O(8)(2-) system destroyed the particular functional groups of fluorescing substances (i.e., aromatic protein-, tryptophan protein-, humic- and fulvic-like substances) in EPS and caused cleavage of linkages in the polymeric backbone and simultaneous destruction of microbial cells, resulting in the release of EPS-bound water, intracellular materials and water of hydration inside cells, and subsequent enhancement of dewaterability.

Synergetic pretreatment of waste activated sludge by Fe(II)–activated persulfate oxidation under mild temperature for enhanced dewaterability

The potential benefits of Fe(II)-activated persulfate (S(2)O(8)(2-)) oxidation under mild temperature in enhancing the dewaterability of waste activated sludge were investigated. Capillary suction time (CST) was used to characterize sludge dewatering. Zeta potential, particle size distribution, three-dimensional excitation-emission matrix (EEM) fluorescence spectroscopy, fourier-transformed infrared (FT-IR) spectroscopy and scanning electronic microscopy (SEM) were employed to explore influencing mechanisms. The results indicated that the dewaterability was deteriorated with single thermal treatment, but significantly enhanced in the presence of Fe(II)-S(2)O(8)(2-) oxidation and further advanced together with thermal treatment. EEM and FT-IR analysis indicated that combined thermal and Fe(II)-S(2)O(8)(2-) oxidation pretreatment led to degrading of tyrosine and tryptophan protein-like substances in extracellular polymeric substances (EPS) and cleavage of linkages in polymeric backbone. SEM images further revealed the rupture of sludge flocs at the colloidal scale, which contributed to the release of EPS-bound water and interstitial water trapped between flocs, and subsequent enhanced dewaterability.

Innovative combination of electrolysis and Fe(II)-activated persulfate oxidation for improving the dewaterability of waste activated sludge

The feasibility of electrolysis integrated with Fe(II)-activated persulfate (S2O8(2-)) oxidation to improve waste activated sludge (WAS) dewaterability was evaluated. The physicochemical properties (sludge volume (SV), total suspended solids (TSS) and volatile suspended solids (VSS)) and extracellular polymeric substances (EPS), including slime EPS, loosely bound EPS (LB-EPS) and tightly bound EPS (TB-EPS) were characterized to identify their exact roles in sludge dewatering. While dewaterability negatively corresponded to LB-EPS, TB-EPS, protein (PN) and polysaccharide (PS) in LB-EPS and TB-EPS, it was independent of SV, TSS, VSS, slime EPS and PN/PS. Further study through scanning electron microscope (SEM) verified the entrapment of bacterial cells by TB-EPS, protecting them against electrolysis disruption. Comparatively, electrolysis integrated with S2O8(2-)/Fe(II) oxidation was able to effectively disrupt the protective barrier and crack the entrapped cells, releasing the water inside EPS and cells. Therefore, the destruction of both TB-EPS and cells is the fundamental reason for the enhanced dewaterability.

Understanding methane bioelectrosynthesis from carbon dioxide in a two-chamber microbial electrolysis cells (MECs) containing a carbon biocathode.

To better understand the underlying mechanisms for methane bioelectrosynthesis, a two-chamber MECs containing a carbon biocathode was developed and studied. Methane production substantially increased with increasing cathode potential. Considerable methane yield was achieved at a poised potential of -0.9 V (vs. Ag/AgCl), reaching 2.30±0.34 mL after 5 h of operation with a faradaic efficiency of 24.2±4.7%. Confirmatory tests done at 0.9 V by switching the type of flushed substrates (CO2/N2) or the electrical exposure modes (ON/OFF) demonstrated that cathode serving as an electron donor was the vital driving force for methanogenesis occurring at microbe-electrode surface. Fluorescence in situ hybridization reveled Methanobacteriaceae (particularly Methanobacterium) was the predominant methanogens, supporting the mechanisms of direct electron transfer between cell-electrode. Additionally, the analysis of scanning electron microscope confirmed that the multiple pathways of electron transfer, including direct cathode-to-cell, interspecies exchange and semi-conductive conduits all together ensured the successful electromethanogenesis process.

Biocatalysis conversion of methanol to methane in an upflow anaerobic sludge blanket (UASB) reactor: Long-term performance and inherent deficiencies.

Long-term performance of methanol biocatalysis conversion in a lab-scale UASB reactor was evaluated. Properties of granules were traced to examine the impact of methanol on granulation. Methanolic wastewater could be stably treated during initial 240d with the highest biogas production rate of 18.6 ± 5.7 L/Ld at OLR 48 g-COD/Ld. However, the reactor subsequently showed severe granule disintegration, inducing granule washout and process upsets. Some steps (e.g. increasing influent Ca(2+) concentration, etc.) were taken to prevent rising dispersion, but no clear improvement was observed. Further characterizations in granules revealed that several biotic/abiotic factors all caused the dispersion: (1) depletion of extracellular polymeric substances (EPS) and imbalance of protein/polysaccharide ratio in EPS; (2) restricted formation of hard core and weak Ca-EPS bridge effect due to insufficient calcium supply; and (3) simplification of species with the methanol acclimation. More efforts are required to solve the technical deficiencies observed in methanolic wastewater treatment.

Biomethane recovery from Egeria densa in a microbial electrolysis cell-assisted anaerobic system: Performance and stability assessment.

Renewable energy recovery from submerged aquatic plants such as Egeria densa (E. densa) via continuous anaerobic digestion (AD) represents a bottleneck because of process instability. Here, a single-chamber membrane-free microbial electrolysis cell (MEC) equipped with a pair of Ti/RuO2 mesh electrodes (i.e. the combined MEC-AD system) was implemented at different applied voltages (0-1.0 V) to evaluate the potential effects of bioelectrochemical stimulation on methane production and process stability of E. densa fermentation. The application of MEC effectively stabilized E. densa fermentation and upgraded overall process performance, especially solid matters removal. E. densa AD process was operated steadily throughout bioelectrochemical process without any signs of imbalance. The solubilization-removal of solid matters and methane conversion efficiency gradually increased with increasing applied voltage, with an average methane yield of approximately 248.2 ± 21.0 mL L(-1) d(-1) at 1.0 V. Whereas, the stability of the process became worse immediately once the external power was removed, with weaken solid matters removal along with methane output, evidencing the favorable and indispensable role in maintaining process stability. The stabilizing effect was further quantitatively demonstrated by statistical analysis using standard deviation (SD), coefficient of variance (CV) and box-plots. The syntrophic and win-win interactions between fermenting bacteria and electroactive bacteria might have contributed to the improved process stability and bioenergy recovery.

Effect of influent COD/SO42− ratios on biodegradation behaviors of starch wastewater in an upflow anaerobic sludge blanket (UASB) reactor

A lab-scale upflow anaerobic sludge blanket (UASB) has been run for 250days to investigate the influence of influent COD/SO4(2-) ratios on the biodegradation behavior of starch wastewater and process performance. Stepwise decreasing COD/SO4(2-) ratio enhanced sulfidogenesis, complicating starch degradation routes and improving process stability. The reactor exhibited satisfactory performance at a wide COD/SO4(2-) range ⩾2, attaining stable biogas production of 1.15-1.17LL(-1)d(-1) with efficient simultaneous removal of total COD (73.5-80.3%) and sulfate (82.6±6.4%). Adding sulfate favored sulfidogenesis process and diversified microbial community, invoking hydrolysis-acidification of starch and propionate degradation and subsequent acetoclastic methanogenesis; whereas excessively enhanced sulfidogenesis (COD/SO4(2-) ratios <2) would suppress methanogenesis through electrons competition and sulfide inhibition, deteriorating methane conversion. This research in-depth elucidated the role of sulfidogenesis in bioenergy recovery and sulfate removal, advancing the applications of UASB technology in water industry from basic science.

Biogas recirculation for simultaneous calcium removal and biogas purification within an expanded granular sludge bed system treating leachate.

Biogas, generated from an expanded granular sludge bed (EGSB) reactor treating municipal solid waste (MSW) leachate, was recirculated for calcium removal from the leachate via a carbonation process with simultaneous biogas purification. Batch trials were performed to optimize the solution pH and imported biogas (CO2) for CaCO3 precipitation. With applicable pH of 10-11 obtained, continuous trials achieved final calcium concentrations of 181-375 mg/L (removal efficiencies≈92.8-96.5%) in the leachate and methane contents of 87.1-91.4% (purification efficiencies≈65.4-82.2%) in the biogas. Calcium-balance study indicates that 23-986 mg Ca/d was released from the bio-system under the carbonized condition where CaCO3 precipitating was moved outside the bioreactor, whereas 7918-9517 mg Ca/d was trapped into the system for the controlled one. These findings demonstrate that carbonation removal of calcium by biogas recirculation could be a promising alternative to pretreat calcium-rich MSW leachate and synergistically to improve methane content.

Response of morphology and microbial community structure of granules to influent COD/SO42 – ratios in an upflow anaerobic sludge blanket (UASB) reactor treating starch wastewater

Biochemical properties of granules are of vital importance to UASB performance. This study characterized the granules cultivated at different COD/SO42- ratios to elucidate the influence of sulfidogenesis on starch wastewater (1000 mg-COD L-1) biodegradation kinetics and process stability. Suitable sulfate addition enriched granular microecosystems and stimulated the secretion of extracellular substances, facilitating cells cohersion and sludge aggregation. The percentage of granules larger than 2.8 mm increased from <10.0% to 58.8-69.4% with decreasing COD/SO42- ratio from 10 to 2. Starch-fed granules tended to grow flagella-like filaments on the surface. The filaments overwhelmed by hydrophilic biopolymers had high affinity for biogas-bubbles and water-molecules aggravating granule floatation and washout. 16 s rRNA gene analysis revealed that decreasing COD/SO42- ratio shifted Syntrophobacterales to Desulfovibrio, which co-worked with Methanosaeta while suppressing Methanobacterium thereby altering starch bioconversion routes. Decrease in Syntrophobacterales caused propionate accumulation and slight process upset.