Search

Treatment of greywater by electrocoagulation using aluminum electrodes was studied. The effects of current-density, electrolysis-time, and inter-electrode-gap on turbidity-removal and electrical-energy consumption were investigated. Under the optimal conditions (J= 12.5 mA/cm2,t= 30 min, andl= 0.5 cm), pollutants removal were: CODtotal= 52.8%, CODsoluble= 31.4%, BODtotal= 32.8%, BODsoluble= 27.6%, SS = 64.6%, TN = 30.1%, and TP = 13.6%. The consumed electrical-energy recorded 4.1 kWh/m3with an operating cost 0.25 US $/m3. Artificial intelligence was developed to simulate the influence of variables on the turbidity-removal. A 3–6–1 neural network achievedR-values: 0.99 (training), 0.84 (validation) and 0.89 (testing). An adaptive neuro-fuzzy inference system indicated that current-density is the most influential input. [ABSTRACT FROM AUTHOR]

Photocatalysts promised to control pollution in an environmentally benign manner, inexpensively, and with a low or cheap energy input. However, the limited chemical activity of photocatalysts has prevented their widespread use. This limitation has two important consequences; in addition to limited removal efficiency for pollution, photocatalysts may also generate unwanted byproducts due to incomplete reaction. This study focuses on the byproducts formed in the photocatalytic degradation of dimethyl sulfide (DMS) on titanium dioxide (TiO2), using a continuous flow reactor and detection via proton transfer reaction mass spectrometry. TiO2, activated carbon (AC), TiO2/AC (1:1) and TiO2/AC (1:5) were tested using either a laser-driven light source or LED lamps at 365 nm. The samples were characterized using a N2-BET surface area and pore size distributions, Scanning Electron Microscopy, X-ray Diffraction, and X-ray Photoelectron Spectroscopy, which confirmed that TiO2 was successfully coated on activated carbon without unexpected phases. TiO2 and activated carbon showed different removal mechanisms for DMS. The maximum yield of formaldehyde, 11.4%, was observed for DMS reacting on a TiO2/AC (1:5) composite operating at a DMS removal efficiency of 31.7% at 50 ∘ C. In addition to formaldehdye, significant products included acetone and dimethyl disulfide. In all, observed byproducts accounted for over half of the DMS material removed from the airstream. The TiO2/AC (1:5) and TiO2/AC (1:1) composites have a lower removal efficiency than TiO2, but a higher yield of byproducts. Experiments conducted from 20 ∘ C to 70 ∘ C showed that as temperature increases, the removal efficiency decreases and the production of byproducts increases even more. This is attributed both to decreased surface activity at high temperatures due to increased recombination of reactive species, and to the decreased residence time of volatile compounds on a hot surface. This study shows that potentially dangerous byproducts are formed by photocatalytic reactors because the reaction is incomplete under the conditions generally employed. [ABSTRACT FROM AUTHOR]

The comprehensive characterization of per- and polyfluoroalkyl substances (PFASs) is necessary for the effective assessment and management of risk at contaminated sites. While current analytical methods are capable of quantitatively measuring a number of specific PFASs, they do not provide a complete picture of the thousands of PFASs that are utilized in commercial products and potentially released into the environment. These unmeasured PFASs include many PFAS precursors, which may be converted into related PFAS chemicals through oxidation. The total oxidizable precursor (TOP) assay offers a means of bridging this gap by oxidizing unknown PFAS precursors and intermediates and converting them into stable PFASs with established analytical standards. The application of the TOP assay to samples from PFAS-contaminated sites has generated several new insights, but it has also presented various technical challenges for laboratories. Despite the increased number of literature studies that include the TOP assay, there is a critical and growing gap in the application of this method beyond researchers in academia. This article outlines the benefits and challenges of using the TOP assay with aqueous samples for site assessments and suggests ways to address some of its limitations.

Microplastics in the aquatic system are among the many inevitable consequences of plastic pollution, which has cascading environmental and public health impacts. Our study aimed at analyzing surface interactions and leachate production of six microplastics under ultraviolet (UV) irradiation. Leachate production was analyzed for the dissolved organic content (DOC), UV 254 , and fluorescence through excitation emission (EEM) to determine the kinetics and mechanisms involved in the release of organic matter by UV irradiation. The results suggested there was a clear trend of organic matter being released from the surface of the six microplastics caused by UV irradiation based on DOC, UV 254 absorbance, and EEM intensity increasing with time. Polystyrene had the greatest and fastest increase in DOC concentrations, followed by the resin coated polystyrene. Experiments conducted at different temperatures indicated the endothermic nature of these leaching mechanisms. The differences in leachate formation for different polymers were attributed to their chemical makeup and their potency to interact with UV. The aged microplastic samples were analyzed by Fourier-transform infrared spectroscopy (FT-IR), Raman, and X-ray photoelectron spectroscopy (XPS), to determine the surface changes with respect to leachate formation. Results indicated that all microplastics had increasing carbonyl indices when aged by UV with polystyrene being the greatest. These findings affirm that the leachate formation is an interfacial interaction and could be a significant source of organic compound influx to natural waters due to the extremely abundant occurrence of microplastics and their large surface areas., Competing Interests: Conflicts of interest There is no competing financial interest between authors.

With growing environmental consciousness, biomaterials (BMs) have garnered attention as sustainable materials for the adsorption of hazardous water contaminants. These BMs are engineered using surface treatments or physical alterations to enhance their adsorptive properties. The lab-scale methods generally employ a One Variable at a Time (OVAT) approach to analyze the impact of biomaterial modifications, their characteristics and other process variables such as pH, temperature, dosage, etc ., on the removal of metals via adsorption. Although implementing the adsorption procedure using BMs seems simple, the conjugate effects of adsorbent properties and process attributes implicate complex nonlinear interactions. As a result, artificial neural networks (ANN) have gained traction in the quest to understand the complex metal adsorption processes on biomaterials, with applications in environmental remediation and water reuse. This review discusses recent progress using ANN frameworks for metal adsorption using modified biomaterials. Subsequently, the paper comprehensively evaluates the development of a hybrid-ANN system to estimate isothermal, kinetic and thermodynamic parameters in multicomponent adsorption systems., Competing Interests: Conflicts of interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Per- and polyfluoroalkyl substances (PFAS) are a set of synthetic chemicals which contain several carbon-fluorine (C-F) bonds and have been in production for the past eight decades. PFAS have been used in several industrial and consumer products including nonstick pans, food packaging, firefighting foams, and carpeting. PFAS require proper investigations worldwide due to their omnipresence in the biotic environment and the resulting pollution to drinking water sources. These harmful chemicals have been associated with adverse health effects such as liver damage, cancer, low fertility, hormone subjugation, and thyroid illness. In addition, these fluorinated compounds show high chemical, thermal, biological, hydrolytic, photochemical, and oxidative stability. Therefore, effective treatment processes are required for the removal and degradation of PFAS from wastewater, drinking water, and groundwater. Previous review papers have provided excellent summaries on PFAS treatment technologies, but the focus has been on the elimination efficiency without providing mechanistic understanding of removal/degradation pathways. The present review summarizes a comprehensive examination of various thermal and non-thermal PFAS destruction technologies. It includes sonochemical/ultrasound degradation, microwave hydrothermal treatment, subcritical or supercritical treatment, electrical discharge plasma technology, thermal destruction methods/incinerations, low/high-temperature thermal desorption process, vapor energy generator (VEG) technology and mechanochemical destruction. The background, degradation mechanisms/pathways, and advances of each remediation process are discussed in detail in this review., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Bacterial regrowth after water/wastewater disinfection poses severe risks to public health. However, regrowth studies under realistic water conditions that might critically affect bacterial regrowth are scarce. This study aimed to assess for the first time the regrowth of Escherichia coli ( E. coli ) in terms of its viability and culturability in environmental waters after chlorine disinfection, which is the most widely used disinfection method. Post-chlorination regrowth tests were conducted in 1) standard 0.85% NaCl solution, 2) river water receiving domestic wastewater effluents, and 3) river water that is fully recharged by domestic wastewater effluents. The multiplex detection of plate count and fluorescence-based viability test was adopted to quantify the culturable and viable E. coli to monitor the regrowth process. The results confirmed that chlorine treatment (0.2, 0.5 and 1.0 mg L -1 initial free chlorine) induced more than 99.95% of E. coli to enter a viable but non-culturable (VBNC) state and the reactivation of VBNC E. coli is presumably the major process of the regrowth. A second-order regrowth model well described the temporal shift of the survival ratio of culturable E. coli after the chlorination ( R 2 : 0.73-1.00). The model application also revealed that the increase in initial chlorine concentration and chlorine dose limited the maximum regrowth rate and the maximum survival ratio, and the regrowth rate and percentage also changed with the water type. This study gives a better understanding of the potential regrowth after chlorine disinfection and highlights the need for investigating the detailed relation of the regrowth to environmental conditions such as major components of water matrices., Competing Interests: Conflicts of interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Estrone (E1), 17α-estradiol (17α-E2), 17β-estradiol (17β-E2), and estriol (E3) are persistent in livestock manure and present serious pollution concerns because they can trigger endocrine disruption at part-per-trillion levels. This study conducted a global analysis of estrogen occurrence in manure using all literature data over the past 20 years. Besides, predicted environmental concentration (PEC) in soil and water was estimated using fate models, and risk/harm quotient (RQ/HQ) methods were applied to screen risks on children as well as on sensitive aquatic and soil species. The estradiol equivalent values ranged from 6.6 to 4.78 × 10 4  ng/g and 12.4 to 9.46 × 10 4  ng/L in the solid and liquid fraction. The estrogenic potency ranking in both fractions were 17β-E2> E1>17α-E2>E3. RQs of measured environmental concentration in the liquid fraction pose medium (E3) to high risk (E1, 17α-E2 & 17β-E2) to fish but are lower than risks posed by xenoestrogens. However, the RQ of PECs on both soil organisms and aquatic species were insignificant (RQ < 0.01), and HQs of contaminated water and soil ingestion were within acceptable limits. Nevertheless, meticulous toxicity studies are still required to confirm (or deny) the findings because endocrine disruption potency from mixtures of these classes of compounds cannot be ignored., (Copyright © 2021. Published by Elsevier Ltd.)

Magnetic carbon nanotube (MCNT) composites with titanium dioxide (TiO 2 ) have an enhanced photocatalytic disinfection efficiency (i.e. higher disinfection rate) and better applicability (i.e. solar light applicability and catalyst separation using its magnetic property) than bare TiO 2 and/or MCNT. However, the role and mechanism of MCNT in the disinfection process are still unclear. Therefore, this study aimed at investigating the disinfection mechanism of Escherichia coli using MCNT-TiO 2 nanocomposites under various conditions (i.e. the presence and absence of light and reactive oxygen species scavengers, and different MCNT-TiO 2 ratio) and photocatalytic disinfection models. The results showed that (i) MCNT and its nanocomposites with TiO 2 had much higher disinfection efficiencies than bare TiO 2 , (ii) the physical bacterial capture was the dominant disinfection mechanism, (iii) the higher disinfection rate was found at an optimum MCNT:TiO 2 ratio of 5:1 under the tested experimental conditions, (iv) hydroxyl radical (OH) was the influencing reactive oxygen species on the photocatalytic disinfection using MCNT-TiO 2 , and (v) good correlation between experimental parameters (i.e. carbon contents, surface area and concentration of MCNT-TiO 2 ) and the contribution rate of physical and photocatalysis reactions. The finding from this study and the methods proposed herein are essential for understanding the photocatalytic disinfection processes using TiO 2 and its carbonaceous nanocomposites, which can promote the application of photocatalytic disinfection process., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

The high concentrations of pharmaceuticals and personal care products (PPCP) that found in water in many locations are of concern. Among the available water treatment methods, heterogeneous photocatalysis using TiO 2 is an emerging and viable technology to overcome the occurrence of PPCP in natural and waste water. The combination of carbonaceous materials (e.g., activated carbon, carbon nanotubes and graphene nanosheets) with TiO 2 , a recent development, gives significantly improved performance. In this article, we present a critical review of the development and fabrication of carbonaceous-TiO 2 and its application to PPCP removal including its influence on water chemistry, and the relevant operational parameters. Finally, we present an analysis of current priorities in the ongoing research and development of carbonaceous-TiO 2 for the photodegradation of PPCP., (Copyright © 2018 Elsevier Ltd. All rights reserved.)