Wenxin Shi

High concentration powdered activated carbon-membrane bioreactor (PAC-MBR) for slightly polluted surface water treatment at low temperature.

In this study, different concentrations of PAC combined with MBR were carried out to treat slightly polluted surface water (SPSW) at low temperature (10°C). Effects of PAC on the efficiencies of operation, treatment, and the performance of the process were investigated. It was found that the effluent quality, performance efficiency, resistance of shock load were all enhanced and chemical irreversible membrane fouling was reduced with increasing dosage of PAC in MBR. Only when the concentration of PAC which acted as biological carriers was high enough (i.g., 50 g/L), nitrification without initial inoculation in the filtration tank could start within 19 days and be completed within 35 days at 10°C. Fifty grams per liter PAC was the optimal dosage in MBR for stable and extended operation. Under this condition, mean removal efficiencies of ammonia nitrogen (NH(3)-N), dissolved organic carbon (DOC) and UV(254) were 93%, 75%, and 85%, respectively.

Optimization of complex conditions by response surface methodology for APAM–oil/water emulsion removal from aqua solutions using nano-sized TiO2/Al2O3 PVDF ultrafiltration membrane

This paper studies the cumulative effect of various parameters, namely anionic polyacrylamide (APAM) concentration, oil concentration, pH, trans-membrane pressure (TMP), and total dissolved solid (TDS), and obtains optimal parameters for the minimum relative flux (J/J(0)) declining in aqueous solutions with response surface methodology (RSM). In order to analyze the mutual interaction and optimal values of parameters affecting ultrafiltration, a central composite rotatable design (CCRD), one method of RSM, was employed. The analysis of variance (ANOVA) of the cubic polynomial model demonstrated that this model was highly significant and reliable. The results show that the effect of APAM and oil on J/J(0) has an inverse trend with pH value increasing. Moreover, the mutual interaction of initial APAM (oil) concentration (C(APAM(oil))) and pH (TMP) were negligible, while the mutual interaction of C(APAM) and C(oil) has an obvious effect, i.e. the effect of initial feed C(APAM) became more important at higher values of initial feed C(oil), and the J/J(0) was only about 4%. The favorable operate conditions in this ultrafiltration process were at low C(APAM), C(oil), pH, and TMP, which agreed with the conclusions of many authors, while considering water production, C(APAM) and C(oil) < 50 mg/L, pH < 4, and TMP < 0.075 MPa could be accepted.

Highly Efficient Phosphate Scavenger Based on Well-Dispersed La(OH)3 Nanorods in Polyacrylonitrile Nanofibers for Nutrient-Starvation Antibacteria

La(OH)3 nanorods immobilized in polyacrylonitrile (PAN) nanofibers (PLNFs) were fabricated for the first time by electrospinning and a subsequent in situ surfactant-free precipitation method and then applied as a highly efficient phosphate scavenger to realize nutrient-starvation antibacteria for drinking water security. The immobilization by PAN nanofibers effectively facilitated the in situ formation of the aeolotropic and well-dispersed La(OH)3 nanostructures and, thus, rendered higher phosphate removal efficiency due to more exposed active sites for binding phosphate. The maximum phosphate capture capacity of La(OH)3 nanorods in PAN nanofibers was around 8 times that of the La(OH)3 nanocrystal fabricated by precipitation without PAN protection. Moreover, remarkably fast adsorption kinetics and high removal rate were observed toward low concentration phosphate due to the high activity of our materials, which can result in a stringent phosphate-deficient condition to kill microorganisms in water effectively. The present material is also capable of preventing sanitized water from recontamination by bacteria and keeping water biologically stable for drinking. Impressively, stabilized by PAN nanofibers, the La(OH)3 nanorods can be easily separated out after reactions and avoid leaking into water. The present development has great potential as a promising antimicrobial solution for practical drinking water security and treatment with a negligible environmental footprint.

Heterogeneous activation of peroxymonosulfate by amorphous boron for degradation of bisphenol S.

Recently, tremendous efforts have been devoted to developing carbon-based metal-free catalysts as an alternative to metal-based catalysts for remediation of emerging contaminants. However, further investigations have demonstrated that the durability of carbocatalysts is poor. Therefore, it is extremely desirable to seek a novel metal-free catalyst with high efficiency and superb stability. Herein, we first discovered that amorphous boron (A-boron) can be used as a metal-free catalyst for peroxymonosulfate (PMS) activation to produce free radicals for effective degradation of bisphenol S (BPS), which is a newly-occurring estrogenic endocrine-disrupting chemical. It exhibited outstanding catalytic activity and superior stability as comparing to metal-based and metal-free carbon-based catalysts. Moreover, many other typical organic pollutants in water such as bisphenol F, sulfamethoxazole, rhodamine B and methyl orange can also be effectively decomposed in A-boron/PMS oxidative system. The effects of reaction parameters on BPS degradation were systematically investigated. The catalytic oxidation mechanism was proposed. The intriguing catalytic feature of A-boron discovered in this study will provide new opportunities for the future development of A-boron based materials with promising applications in water remediation.

Enhanced adsorption of the cationic dyes in the spherical CuO/meso-silica nano composite and impact of solution chemistry

In this study, the spherical mesoporous silica (meso-silica MCM-41) and that inorganically modified with CuO (CuO/MCM-41 nano composite) were synthesized and characterized. It was demonstrated that CuO were successfully loaded in the synthesized nano composite CuO/MCM-41. Importantly, the loaded CuO had a significant enhancement effect on the adsorption of Crystal violet and Methylene blue. Adsorption kinetic of the tested cationic dyes in the synthesized materials fitted the pseudo-second-order kinetic model and Webers intra-particle diffusion model well. According to the Langmuir isotherm model, the maximum adsorption capacities (Qmax) of the CuO/MCM-41 towards Crystal violet and Methylene blue increased to 52.9 and 87.8mg/g, while those of the pure MCM-41 were 46.2 and 65.7mg/g, respectively. Due to the surface charge of CuO and the protonation of the dye molecules, the electrostatic forces between the loaded CuO and the organic cationic dyes contributed to the enhancement effect. Additionally, the presented results indicated that the adsorption of the cationic dyes in the CuO/MCM-41 depended on pH and ion strength of the solution but insignificantly on the coexisted humic acid due to the mesoporous character of CuO/MCM-41 nano composite.

Comparative performance between intermittently cyclic activated sludge-membrane bioreactor and anoxic/aerobic-membrane bioreactor.

A process of intermittently cyclic activated sludge-membrane bioreactor (ICAS-MBR) was developed to enhance the performance of biological phosphorus removal (EBPR), which was constructed under sequencing anoxic/anaerobic/aerobic condition. The performance between ICAS-MBR and conventional anoxic/aerobic-membrane bioreactor (A/O-MBR) in terms of phosphorus removal, nitrification performance and microbial aspects were investigated in this study. The experimental results indicated that the phosphorus removal efficiency in ICAS-MBR process increased from 65% to 83% when compared with A/O-MBR. It was also found that the COD removal efficiencies of the two processes were over 94%, and NH(4)(+)-N and TN average removal efficiencies were 96% and 69% in ICAS-MBR and 96% and 78% in A/O-MBR, respectively. Furthermore, micrographs observation obtained confirmed the succession and diversification of microorganisms in the two systems followed a similar regularity.

Membrane fouling of forward osmosis (FO) membrane for municipal wastewater treatment: A comparison between direct FO and OMBR.

In this work, membrane fouling behavior in a direct forward osmosis (FO) and an osmotic membrane bioreactor (OMBR) for municipal wastewater treatment was systematically investigated and compared. During the long-term operation, much severer flux decline was observed for the direct FO than that for the OMBR. The cake layer was found to be much thicker, together with large amounts of microorganisms growing on the membrane surface in direct FO. Interestingly, no obvious attachment of microorganisms on the membrane surface was observed in the OMBR. The fourier transform infrared spectroscopy (FTIR) and excitation emission matrices (EEM) analyses showed the polysaccharides and proteins were the dominant organic foulants in the fouling layer, and the quantity of the organic substances was also higher in direct FO than that in OMBR. Energy-dispersive X-ray (EDX) results indicated the main inorganic elements in the fouling layer were Ca, Mg, Fe and P, all of which exhibited higher relative percentages in direct FO than that in OMBR. The occurrence of higher contents of microorganisms, organic foulants and inorganic elements in the cake layer caused a higher filtration resistance for the FO membrane in the direct FO. Although more severe membrane fouling was identified in direct FO, the hydraulic and chemical cleaning was more effective on recovering the water permeability of the membrane in direct FO than that in OMBR.

Efficient As(III) removal by magnetic CuO-Fe3O4 nanoparticles through photo-oxidation and adsorption under light irradiation

A novel bifunctional CuO-Fe3O4 magnetic material was synthesized and characterized, to remove As(III) through photo-oxidation and adsorption. Photo-oxidation of As(III), adsorption characteristics of CuO-Fe3O4 nanoparticles, the effect of solution pH, ionic strength and coexisting ions on As(III) removal were investigated. Under light irradiation, As(III) could be completely oxidized to less toxic As(V) by CuO-Fe3O4 nanoparticles within 60min in the photo-oxidation reaction. Simultaneously, As(V) could be adsorbed onto the surface of nanoparticles with high efficiency. The adsorption of As(V) was well fitted by the pseudo-second-order model and the Freundlich isotherm model, respectively, and the maximum adsorption capacities of the nanoparticles was 118.11mg/g at pH 7.0. As(III) could be effectively removed by CuO-Fe3O4 nanoparticles at initial pH range from 4 to 8. Among all the common coexisting ions investigated, except for chloride and sulfate, carbonate, silicate and phosphate decreased the As(III) removal by competing with arsenic species for adsorption sites. The synthesized magnetic CuO-Fe3O4 combined the photocatalytic property of CuO and the high adsorption capacity of both CuO and Fe3O4, which make it have significant potential applications in the arsenic wastewater treatment.

Isotherm and kinetic behavior of adsorption of anion polyacrylamide (APAM) from aqueous solution using two kinds of PVDF UF membranes.

To determine the isotherm parameters and kinetic parameters of adsorption of anion polyacrylamide (APAM) from aqueous solution on PVDF ultrafiltration membrane (PM) and modified PVDF ultrafiltration membrane (MPM) is important in understanding the adsorption mechanism of ultrafiltration processes. Effect of variables including adsorption time, initial solution concentration, and temperature were investigated. The Redlich-Peterson equation of the five different isotherm models we chose was the most fitted model, and the R(2) was 0.9487, 0.9765 for PM and MPM, respectively; while, the pseudo-first-order model was the best choice among all the four kinetic models to describe the adsorption behavior of APAM onto membranes, suggesting that the adsorption mechanism was a chemical and physical combined adsorption on heterogeneous surface. The thermodynamic parameters were also calculated from the temperature dependence (Δ(r)G(m)(θ), Δ(r)H(m)(θ), Δ(r)S(m)(θ)), which showed that the process of adsorption is not spontaneous but endothermic process and high temperature favors the adsorption.

Separation of oil/water emulsion using nano-particle (TiO2/Al2O3) modified PVDF ultrafiltration membranes and evaluation of fouling mechanism

In the present study, nano-sized TiO(2)/Al(2)O(3) modified polyvinylidene fluoride (PVDF) membranes (MM) were fabricated and then utilized for oil/water emulsion separation. The results showed that, compared with PVDF membrane (OM), the contact angle of MM decreased and hydrophilicity increased. The ultrafiltration (UF) of oil in water emulsions with transmembrane pressure (TMP) increasing results in a sharp fall in relative flux with time. The cake filtration models did not always predict the performance over the complete range of filtration times very well. In the initial 30 min, all the four cake models can simulate this UF process to a certain extent, and the suitability was: cake filtration > intermediate pore blocking > standard pore blocking > complete pore blocking models. However, they were no longer adapted well with UF time extent to 60 min, but only cake filtration (R(2) = 0.9535) maintained a high adaptability. Surface and cross-sectional morphology of the membrane was investigated by SEM to make an advanced certificate of this UF mechanism.