Lijie Zhou

Enhanced struvite recovery from wastewater using a novel cone-inserted fluidized bed reactor.

The feasibility of struvite recovery at low (12.5 mg/L) and high (120 mg/L) phosphorus concentrations was studied by constructing a novel fluidized bed reactor with cones (FBRwc) and without cones (FBRwoc). The crystallization process was continuously operated for 133 days under different hydraulic retention times (HRT = 1-10 hr), pH (7.5-10), and molar ratios of Mg/P (0.75-1.75), N/P (1-10) and Ca/Mg (0-2). The optimum operating conditions of HRT, pH, Mg/P and N/P molar ratios were found to be 2 hr, 9, 1.25, and 7.5, respectively. Under these optimum conditions, the phosphorus precipitation efficiencies of FBRwc were 93% for low and 98% for high phosphorus influent; however, the efficiencies were 78% and 81% for FBRwoc, respectively. Due to crystal losses at each junction (17%-31%), the crystal recovery efficiency of FBRwoc was relatively low (47%-65%) for both influent concentrations. However, the losses were minimal in FBRwc, which showed 75% and 92% crystal recovery for low and high phosphorus concentrations, respectively. At low calcium concentration, crystal chemical analysis showed the product to be pure struvite (> 99%). The scanning electron microscope and X-ray diffraction results further confirmed that the crystal recovered from FBRwc contained pure struvite, which could be considered a high quality fertilizer. Except HRT, all parameters (pH, Mg/P, N/P and Ca/Mg) were found to be influencing factors for FBRwc performance. Overall, inserting cones in each part of the reactor played a significant role in enhancing struvite recovery from a wide range of phosphorus-containing wastewater.

Effects of suspended titanium dioxide nanoparticles on cake layer formation in submerged membrane bioreactor.

Effects of the suspended titanium dioxide nanoparticles (TiO2 NPs, 50 mg/L) on the cake layer formation in a submerged MBR were systematically investigated. With nanometer sizes, TiO2 NPs were found to aggravate membrane pore blocking but postpone cake layer fouling. TiO2 NPs showed obvious effects on the structure and the distribution of the organic and the inorganic compounds in cake layer. Concentrations of fatty acids and cholesterol in the cake layer increased due to the acute response of bacteria to the toxicity of TiO2 NPs. Line-analysis and dot map of energy-dispersive X-ray were also carried out. Since TiO2 NPs inhibited the interactions between the inorganic and the organic compounds, the inorganic compounds (especially SiO2) were prevented from depositing onto the membrane surface. Thus, the postponed cake layer fouling was due to the changing features of the complexes on the membrane surface caused by TiO2 NPs.

Effects of low-concentration Cr(VI) on the performance and the membrane fouling of a submerged membrane bioreactor in the treatment of municipal wastewater

The effects of low-concentration Cr(VI) (0.4 mg l−1) on the performance of a submerged membrane bioreactor (SMBR) in the treatment of municipal wastewater, as well as membrane fouling were investigated. Compared with the SMBR for control municipal wastewater, the SMBR for Cr(VI)-containing municipal wastewater had a higher concentration of soluble microbial products (SMP) with lower molecular weights, and smaller sludge particle sizes. Furthermore, low-concentration Cr(VI) induced membrane fouling, especially irreversible membrane pore blocking, which markedly shortened the service life of the membrane.

Influence and mechanism of N-(3-oxooxtanoyl)-L-homoserine lactone (C8-oxo-HSL) on biofilm behaviors at early stage

N-acyl-homoserines quenching, enzymatic quenching of bacterial quorum sensing, has recently applied to mitigate biofilm in membrane bioreactor. However, the effect of AHLs on the behavior of biofilm formation is still sparse. In this study, Pseudomonas aeruginosa biofilm was formed on ultra-filtration membrane under a series of N-(3-oxooxtanoyl)-L-homoserine lactone (Cs-oxo-HSL) concentrations. Diffusing C8-oxo-HSL increased the growth rate of cells on biofilm where the concentration of C8-oxo-HSL was over 10(-7) g/L. The C8-oxo-HSL gradient had no observable influence on cell density and extracellular polymeric substances of biofilm with over 10(-7) g/L C8-oxo-HSL. Surprisingly, 10(-11)-10(-8) g/L of C8-oxo-HSL had no effect on cell growth in liquid culture. The cell analysis demonstrated that the quorum sensing system might enhance the growth of neighboring cells in contact with surfaces into biofilm and may influence the structure and organization of biofilm.

Enhanced visible light photocatalytic activity of a floating photocatalyst based on B–N-codoped TiO2 grafted on expanded perlite

Floating photocatalysts of boron–nitrogen codoped TiO2 grafted on expanded perlite (B–N-TiO2/EP) were prepared by a facile sol–gel method. The catalysts were characterized by thermogravimetric differential thermal analysis (TG-DTA), X-ray diffraction (XRD), N2 adsorption–desorption (BET), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS) and UV-vis diffuse reflectance spectroscopy (UV-vis-DRS). The results showed that by modifying the boron doping content in B–N-TiO2/EP, we could effectively obtain photocatalysts with a high BET surface area and porosity. Increasing the boron doping contents would inhibit the transformation of anatase TiO2 to the rutile phase. Compared with N-TiO2/EP, B–N-TiO2/EP exhibits an evident red-shift of the absorption band edge and the absorption intensity of the visible region increases obviously. The enhanced RhB photodegradation rate of B0.57–N-TiO2/EP could reach 94% after 3 h of visible light irradiation. Moreover, the floating photocatalyst could be easily separated and reused, showing great potential for practical applications in environmental cleanup and solar energy conversion.

Structure and distribution of inorganic components in the cake layer of a membrane bioreactor treating municipal wastewater.

A laboratory-scale submerged anoxic-oxic membrane bioreactor treating municipal wastewater was operated to investigate the structure and distribution of the inorganic cake layer buildup on the membrane. BCR (European Community Bureau of Reference) sequential extraction, X-ray photoelectron spectroscopy (XPS), and both map and line scan of energy-dispersive X-ray analysis (EDX) were performed for cake layer characterization. BCR results showed that Si, Al, Ca, Mg, Fe, and Ba were the predominant inorganic elements in the cake layer, and they occurred mostly as crystal particles. Crystal SiO2 was the dominant inorganic compound while Ca in the form of CaSO4 (dominant) and CaCO3 were also present, but exerted little effect on the cake layer structure because most of these compounds were deposited as precipitates on the reactor bottom. EDX results indicated that Si and Al accumulated together along the cross-sectional cake layer in the form of Si-Al (SiO2-Al2O3) crystal particles.

Bioreduction of vanadium (V) in groundwater by autohydrogentrophic bacteria: Mechanisms and microorganisms.

As one of the transition metals, vanadium (V) (V(V)) in trace amounts represents an essential element for normal cell growth, but becomes toxic when its concentration is above 1mg/L. V(V) can alter cellular differentiation, gene expression, and other biochemical and metabolic phenomena. A feasible method to detoxify V(V) is to reduce it to V(IV), which precipitates and can be readily removed from the water. The bioreduction of V(V) in a contaminated groundwater was investigated using autohydrogentrophic bacteria and hydrogen gas as the electron donor. Compared with the previous organic donors, H2 shows the advantages as an ideal electron donor, including nontoxicity and less production of excess biomass. V(V) was 95.5% removed by biochemical reduction when autohydrogentrophic bacteria and hydrogen were both present, and the reduced V(IV) precipitated, leading to total-V removal. Reduction kinetics could be described by a first-order model and were sensitive to pH and temperature, with the optimum ranges of pH7.5-8.0 and 35-40°C, respectively. Phylogenetic analysis by clone library showed that the dominant species in the experiments with V(V) bioreduction belonged to the β-Proteobacteria. Previously known V(V)-reducing species were absent, suggesting that V(V) reduction was carried out by novel species. Their selective enrichment during V(V) bioreduction suggests that Rhodocyclus, a denitrifying bacterium, and Clostridium, a fermenter known to carry out metal reduction, were responsible for V(V) bioreduction.

New insight into the effects of Ca(II) on cake layer structure in submerged membrane bioreactors

The effects of Ca(II) on the structure of the cake layer in submerged membrane bioreactors (SMBRs) were investigated in this study. Three parallel laboratory-scale SMBRs were operated with synthetic municipal wastewater with three Ca(II) levels (82, 208 and 410 mg l−1). As the Ca(II) concentration increased, the sludge floc size increased and the molecular weight of the soluble microbial products (SMP) in the bulk liquid decreased. These observations were attributed to the neutralization and bridging function of Ca(II). Furthermore, Ca(II) addition did not change the thickness of the cake layer, but inhibited the deposition of other elements, such as Al, Si, Mg, and Fe. As a result of Ca(II) addition, the cake layer became less compact and more porous. The interspaces among the flocs in the cake layer helped to reduce the membrane fouling potential.

Potential acute effects of suspended aluminum nitride (AlN) nanoparticles on soluble microbial products (SMP) of activated sludge

The study aims to identify the potential acute effects of suspended aluminum nitride (AlN) nanoparticles (NPs) on soluble microbial products (SMP) of activated sludge. Cultured activated sludge loaded with 1, 10, 50, 100, 150 and 200mg/L of AlN NPs were carried out in this study. As results showed, AlN NPs had a highly inverse proportionality to bacterial dehydrogenase and OUR, indicating its direct toxicity to the activated sludge viability. The toxicity of AlN NPs was mainly due to the nano-scale of AlN NPs. In SMP, AlN NPs led to the decrease of polysaccharide and humic compounds, but had slight effects on protein. The decrease of tryptophan-like substances in SMP indicated the inhibition of AlN NPs on the bacterial metabolism. Additionally, AlN NPs reduced obviously the molecular weight of SMP, which might be due to the nano-scale of AlN.

Efficient visible light-driven in situ photocatalytic destruction of harmful alga by worm-like N,P co-doped TiO2/expanded graphite carbon layer (NPT-EGC) floating composites

The bloom of harmful algae in water has adversely affected water quality, local economies, and human health. Efficient visible light driven floating photocatalysts, namely N,P co-doped TiO2/expanded graphite carbon layer (NPT-EGC) composites, were successfully synthesized using a sol-carbonization method, and then applied as algaecides. The synthesized photocatalysts were characterized by means of XRD, FESEM/EDS, TEM, FTIR spectroscopy, XPS, UV-vis DRS, and PL spectroscopy. The results show that the NPT-EGC composites have a worm-like structure with the N,P co-doped TiO2 particles immobilized on the surface. Among the NPT-EGC photocatalysts with different calcination temperatures, NPT-EGC450 exhibits the highest photocatalytic activity. The removal rate of the algal cells is 98.15% for NPT-EGC450 following 9 h of visible light irradiation. The photocatalytic destruction process can be divided into a rapid adsorption phase and a repeat of the cell reduction phase-lag phase. During the photocatalytic process, the algal cells were damaged as a result of photocatalysis induced oxidation and inhibition. In addition, we simulated the release of MC-LR in the photocatalytic destruction process for the algal cells. The results show that the photocatalyst can remove both the algal cells and MC-LR simultaneously with high efficiency. After three consecutive cycles, the removal rate of the algal cells is still more than 90% for NPT-EGC450, which demonstrates that the NPT-EGC photocatalyst has good reusability and stability.