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1.
Influence of water depth and season on the photodegradation of micropollutants in a free-water surface constructed wetland receiving treated wastewater.
Mathon, B, Coquery, M, Miège, C, Vandycke, A, Choubert, JM
Chemosphere. 2019;:260-270
Abstract
Micropollutants such as pharmaceutical products and pesticides are still present in treated wastewater. Several of these compounds are photoactive, either by direct or indirect photodegradation. An innovative on-site experimental protocol was designed to investigate the contribution of photodegradation processes to eliminate micropolluants in constructed wetland (CW). The solar photodegradation of 23 organic micropollutants was studied using in situ photoreactors at different depths. A CW-photodegradation model was designed and calibrated to further scrutinize the contribution of direct and indirect photodegradation processes in the elimination of micropollutants. The results show that photodegradation is most effective in the first 10 cm of the water column. A classification of micropollutants in 3 groups was developed to characterize their photodegradation. A significant increase of the half-life by direct photodegradation was observed in winter compared to summer due to a lower light intensity in winter. On the opposite, for direct + indirect photodegradation, no significant difference was observed between seasons. The decrease in light intensity in winter was compensated by higher nitrates concentration which promoted the formation of hydroxyl radicals and increased indirect photodegradation. The CW-photodegradation model successfully simulated the measured concentrations for direct and indirect photodegradation for 23 micropolluants. Nonetheless, it overestimated the indirect photodegradation with hydroxyl radicals when using default parameter values derived for surface waters. Hence, the consumption of hydroxyl radicals was increased by a factor of 20 for treated water. This model highlighted the predominance of direct photodegradation in the elimination of all micropollutants, except sotalol for the winter campaign.
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2.
Removal of Acid Orange 51 by micro zero-valent iron under different operational conditions and evaluation of toxicity.
Ghariani, B, Messaoud, M, Louati, I, Mtibaà, R, Nasri, M, Mechichi, T
Environmental science and pollution research international. 2019;(18):18392-18402
Abstract
The removal of Acid Orange 51 (AO 51) dye in aqueous solution by microscale zero-valent iron (m-ZVI) was investigated. The m-ZVI powder was characterized granulometrically by laser particle sizer and morphologically by transmission electron microscopy (TEM). The effects of pH, m-ZVI concentration, H2O2 addition, and dye concentration on the decolorization of AO 51 were experimentally investigated. Results indicate that the removal efficiency is independent from pH values, increases with increasing ZVI dosage, and decreases with dye concentration. With 1 g/L of m-ZVI, AO 51 was effectively removed without and with addition of 25 mM H2O2, yielding a decolorization efficiency of around 70% and 98%, respectively, at pH 3 within 60 min of reaction time. The involvement of ˙OH in oxidizing AO 51 was examined by measuring the removal rates based on ˙OH scavenging molecule. Finally, the disappearance of AO 51 was estimated by monitoring the UV-Vis spectral evolution after 120 min of treatment while the Fourier-Transform Infrared spectroscopy (FT-IR) was performed to verify the occurrence of organic sorption on m-ZVI surface. The scanning electron microscope (SEM) images before and after the reaction illustrated morphological changes on m-ZVI surface. The detoxification of the treated solution was demonstrated using phytotoxicity test.
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3.
Rapid determination of the electroporation threshold for bacteria inactivation using a lab-on-a-chip platform.
Wang, T, Chen, H, Yu, C, Xie, X
Environment international. 2019;:105040
Abstract
Electroporation based locally enhanced electric field treatment (LEEFT) is an emerging bacteria inactivation technology for drinking water disinfection. Nevertheless, the lethal electroporation threshold (LET) for bacteria has not been studied, partly due to the tedious work required by traditional experimental methods. Here, a lab-on-a-chip device composed of platinum electrodes deposited on a glass substrate is developed for rapid determination of the LET. When voltage pulses are applied, an electric field with a linear strength gradient is generated on a channel between the electrodes. Bacterial cells exposed to the electric field stronger than the LET are inactivated, while others remain intact. After a cell staining process to differentiate dead and live bacterial cells, the LETs are obtained by analyzing the fluorescence microscopy images. Staphylococcus epidermidis has been utilized as a model bacterium in this study. The LETs range from 10 kV/cm to 35 kV/cm under different pulsed electric field conditions, decreasing with the increase of pulse width, effective treatment time, and pulsed electric field frequency. The effects of medium properties on the LET were also investigated. This lab-on-a-chip device and the experimental approach can also be used to determine the LETs for other microorganisms found in drinking water.
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4.
Removal of anionic arsenate by a PEI-coated bacterial biosorbent prepared from fermentation biowaste.
Kim, N, Park, M, Yun, YS, Park, D
Chemosphere. 2019;:67-74
Abstract
As a problematic element in water systems, arsenic exists as As(III) and As(V). Adsorption techniques can be used to remove anionic As(V) as it is present as a polyatomic anion. In the case of As(III) which exists in zero-valent state under neutral pH, it can be also removed by adsorption after being converted into As(V). Many inorganic and organic materials have been examined as potential adsorbents for anionic As(V) removal. However, most exhibit relatively low adsorption capacities (<10 mg/g). The objective of this study is to examine As(V)-removal mechanism and practical potential of a PEI-coated bacterial biosorbent prepared from fermentation biowaste. The maximum As(V) uptake of the biosorbent was determined to be 62.99 mg/g by Langmuir model. The effects of various parameters including pH, biosorbent dosage, ionic strength and temperature were also examined. Kinetic and equilibrium models were used to interpret the experimental data mathematically. A 0.01 M NaOH solution was chosen as an effective As(V)-desorbing eluent for biosorbent regeneration. The adsorption capacity of the biosorbent remained above 85% over three successive cycles of adsorption and desorption. In conclusion, the biowaste-driven biosorbent is a promising anion adsorbent for treatment of As(V)-contaminated wasters.
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5.
Photodegradation using TiO2-activated borosilicate tubes.
Khalaf, S, Shoqeir, JH, Scrano, L, Karaman, R, Bufo, SA
Environmental science and pollution research international. 2019;(19):19025-19034
Abstract
This study examines the photocatalytic activity of titanium dioxide (TiO2) semiconductor supported on borosilicate tubes (cut-off 290 nm) towards removal of a mix of persistent organic pollutants (POPs) from water. For this purpose, two widely used analgesic and anti-inflammatory drugs (NSAIDs), ibuprofen (IBU) and mefenamic acid, along with MCPA sodium monohydrate, which is a common herbicide frequently used in the agricultural activities, were selected as a case study. Borosilicate tubes were coated with titanium oxide through two different approaches: sol-gel dip-coating and a hybrid nanoparticle dip-coating and plasma-enhanced chemical vapour deposition (PECVD) process. The photochemical reactor that hosts the titania-coated tubes was designed to permit continuous throughput of liquid feed stream. The photodegradation experiments were performed in laboratory conditions under artificial irradiation simulating solar light. The efficiency of direct photolysis and heterogeneous photocatalysis (TiO2) was investigated, and the performance of each coating method was evaluated. Kinetic studies for each experiment were accomplished, the overall results showed poor efficiency and insufficient removal for NSAIDs through direct photolysis, whereas applying heterogeneous photacatalysis with TiO2 coated on borosilicate tubes was found to accelerate their degradation rate with complete decomposition. Concomitantly, kinetic experimental results showed a critical difference of performance for the two coating methods used; in particular, the degradation rates of pollutants by the sol-gel-coated tubes were much faster than the degradation by the nanoparticle/PECVD-coated tubes. Using TiO2 supported on borosilicate tubes appears to be a promising alternative to conventional TiO2 suspension and avoid post-separation stages. The results achieved in this study can be used to optimise large-scale applications, and expanding the study to cover a wide range of pollutants will lead to achieve more representative results.
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6.
Intermittent light and microbial action of mixed endogenous source DOM affects degradation of 17β-estradiol day after day in a relatively deep natural anaerobic aqueous environment.
Gu, L, Huang, B, Han, F, Xu, Z, Ren, D, He, H, Pan, X, Dionysiou, DD
Journal of hazardous materials. 2019;:40-49
Abstract
All kinds of wastewaters containing steroid estrogens (SEs) and mixed endogenous source dissolved organic matter (DOM) enter natural water environments with intermittent illumination where microbial action occurs in a relatively deep natural aqueous environment. The role of mixed endogenous source DOM in SEs' biodegradation and photochemical degradation in such environments was studied using 17β-estradiol (E2) in laboratory experiments under anaerobic conditions. The experimental results show that microbial action can improve the optical properties and electron transfer capability of mixed endogenous source DOM, promoting photodegradation and biodegradation. Intermittent illumination attenuates DOM's electron transfer capacity and its chromophore groups, but it improves the bioavailability of low molecular weight dissolved organic matter which promotes microbial growth under anaerobic conditions. DOM-mediated co-degradation by light and microbial action over three days was better than either individually. The presence of Fe(III) promoted electron transfer, and Fe(III)-DOM complexes accelerated energy transfer under irradiation, enhancing photodegradation. Any remaining estrogens will continue to degrade, most effectively in well-aerated waters with sufficient illumination.
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7.
Kinetics of chlorate formation during ozonation of aqueous chloride solutions.
Levanov, AV, Isaikina, OY, Gasanova, RB, Uzhel, AS, Lunin, VV
Chemosphere. 2019;:68-76
Abstract
Chlorate ion ClO3- is formed as a result of the complex chemical interaction of ozone with chloride ion in aqueous solution. In neutral and basic solutions, chlorate is the main product. In acid solutions, the main product is molecular chlorine Cl2, and the yield of chlorate is 50-100 times lower. Dependencies have been studied of chlorate formation rate on significant experimental factors: concentrations of initial substances, ozone and chloride ion, acidity (pH), ionic strength and temperature of the reaction solution. The kinetic laws of chlorate generation have been established, and the expressions are given for rate constants of chlorate formation as functions of temperature and ionic strength. When tert-butanol is added to the reaction system, the formation of chlorate ceases, which is an evidence of the crucial role of free radical reactions in this process.
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8.
Influence of algal organic matter of Microcystis aeruginosa on ferrate decay and MS2 bacteriophage inactivation.
Wu, X, Tang, A, Bi, X, Nguyen, TH, Yuan, B
Chemosphere. 2019;:124727
Abstract
Surface water contaminated with algae and with enteric viruses is a global problem. When surface water is used as a drinking water source, it is important to know the influence of algal organic matter on the disinfection of viruses. In this work, we studied the disinfection efficacy of ferrate and the influence of algal organic matter on the disinfection. We determined the MS2 inactivation kinetics by ferrate under three pH conditions (7, 8, and 8.7). The experimental results and pH-dependent calculation suggest that H2FeO4 and HFeO4- are 1935 and 8 times as effective as FeO42- in MS2 inactivation. We also found that intracellular algal organic matter (IAOM) had a stronger effect on MS2 inactivation kinetics than extracellular algal organic matter (EAOM) suggesting that IAOM led to higher consumption of Fe(VI) compared to EAOM. At pH 8.7, while significant consumption of FeO42- by as low as 8 mg C/L of EAOM and 2 mg C/L of IAOM was detected, MS2 inactivation was negatively influenced only when 13 mg C/L of IAOM present. This study showed that it is important to control pH and to determine the concentration of algal organic matter if ferrate is used for disinfection of surface water contaminated with algae.
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9.
Efficient Removal of Diclofenac from Aqueous Solution by Potassium Ferrate-Activated Porous Graphitic Biochar: Ambient Condition Influences and Adsorption Mechanism.
Thi Minh Tam, N, Liu, Y, Bashir, H, Yin, Z, He, Y, Zhou, X
International journal of environmental research and public health. 2019;(1)
Abstract
Porous graphitic biochar was synthesized by one-step treatment biomass using potassium ferrate (K2FeO4) as activator for both carbonization and graphitization processes. The modified biochar (Fe@BC) was applied for the removal of diclofenac sodium (DCF) in an aqueous solution. The as-prepared material possesses a well-developed micro/mesoporous and graphitic structure, which can strengthen its adsorption capacity towards DCF. The experimental results indicated that the maximum adsorption capacity (qmax) of Fe@BC for DCF obtained from Langmuir isotherm simulation was 123.45 mg·L-1 and it was a remarkable value of DCF adsorption in comparison with that of other biomass-based adsorbents previously reported. Thermodynamic quality and effect of ionic strength studies demonstrated that the adsorption was a endothermic process, and higher environmental temperatures may be more favorable for the uptake of DCF onto Fe@BC surface; however, the presence of NaCl in the solution slightly obstructed DCF adsorption. Adsorption capacity was found to be decreased with the increase of solution pH. Additionally, the possible mechanism of the DCF adsorption process on Fe@BC may involve chemical adsorption with the presence of H-bonding and π-π interaction. With high adsorption capacity and reusability, Fe@BC was found to be a promising absorbent for DCF removal from water as well as for water purification applications.
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10.
Research progress and application prospect of anaerobic biological phosphorus removal.
Yang, F, Zhang, C, Rong, H, Cao, Y
Applied microbiology and biotechnology. 2019;(5):2133-2139
Abstract
Anaerobic biological phosphorus removal has proposed a new direction for the removal of phosphorus from wastewater, and the discovery of phosphate reduction makes people have a more comprehensive understanding of microbial phosphorus cycling. Here, from the perspective of thermodynamics, the bioreduction reaction of phosphate was analyzed and its mechanism was discussed. The research progress of phosphate reduction and the application prospects of anaerobic biological phosphorus removal from wastewater were introduced, pointing out the situation and guiding the further research in this field.