Conventional Water Treatment Systems Research Articles

Ozone nanobubble technology as a novel AOPs for pollutants degradation under high salinity conditions

Conventional water treatment systems frequently exhibit diminished efficiency at high salinity - a significant issue especially for real industrial effluents - mostly due to the creation of intricate structures between pollutants and salts. One of the primary obstacles associated with high salinity conditions is the generation of by-products that pose additional hurdles for treatment. In this work, we have investigated the novel advanced oxidation process a so-called ozone nanobubble technology for degradation of the pollutants at high salinity conditions. The mass transfer is often the rate-limiting step in gas-liquid process and the poor rate of mass transfer diminishes the overall efficacy. One of the primary disadvantages associated with ozone is its restricted solubility and instability when dissolved in an aqueous solution. These characteristics impose limitations on its potential applications and need the use of specialized systems to facilitate gas-liquid interaction. In this work, we have also suggested enhancing the ozonation process through the utilization of ozone nanobubbles. The findings of our experiment and subsequent analysis indicate that the presence of nanobubbles enhances the process of ozonation through three key mechanisms: (i) an increased mass transfer coefficient, (ii) a higher rate of reactive oxygen species (ROS) generation attributed to the charged interface, and (iii) the nanobubble interface serving as an active surface for chemical reactions. The predicted mass transfer coefficients were found to range from 3 to 3.5 min−1, a value that is notably greater than that seen for microbubbles. The study showcased the degradation of methylene blue dye through the utilization of ozone nanobubbles, which exhibited a much higher rate of dye degradation compared to ozone microbubbles. The confirmation of the radical degradation mechanism was achieved by the utilization of electron spin resonance (ESR) measurements. The developed process has high potential for application in industrial scale textile wastewater treatment.

Graphene oxide-induced CuO reduction in TiO2/CaTiO3/Cu2O/Cu composites for photocatalytic degradation of drugs via peroxymonosulfate activation

Contamination of water bodies is a global environmental and human health issue. Conventional water treatment systems cannot efficiently eliminate organic contaminants, particularly drugs. Photocatalysis is a promising, environmentally friendly oxidation process for the removal of such compounds. A key point is the choice of material to be used as photocatalyst. Here, TiO2/CaTiO3/Cu2O/Cu composites were fabricated by adding different amounts (x) of graphene oxide (GO) (x wt% = 1, 3, and 5 %) to CaCu3Ti4O12 powder using the solid-state synthesis method. The produced pellets were sintered under inert nitrogen atmosphere at 1100 °C for 3 h. X-ray diffraction analysis showed that the Cu metal amount was increased upon GO addition, and the UV–Vis diffuse reflectance spectroscopy showed that the spectral response was extended to the visible range. Then, high performance liquid chromatography assessment of paracetamol degradation by a photocatalytic cell using TiO2/CaTiO3/Cu2O/Cu composites with different GO amounts showed that the removal efficiency was increased upon introduction of 0.5 mM peroxymonosulfate (PMS) as active component to generate SO4‾ radicals. After 3 h under visible light, 96 % of 10 ppm paracetamol was degraded by the composite with 3 % of GO (1 cm2 surface photocatalyst) compared with 50 % by the composite without GO in the same experimental conditions (PMS in 210 mL of aqueous solution). Free radical trapping and the acute toxicity of potential degradation by-products were also investigated. Our results indicate that TiO2/CaTiO3/Cu2O/Cu with 3 % GO displays long-term stability and durability for the photocatalytic removal of pharmaceutical pollutants from wastewater.

Sistem SCADA Implementasi Sistem SCADA Untuk Proses Koagulasi Pada Instalasi Pengolahan Air Berbasis PLC Schneider M221 dan HMI Weintek

The importance of the need for clean water for human survival so that a water treatment system is needed. Conventional clean water treatment systems require a lot of labor and direct supervision from the operator. One of the automatic water treatment system innovations is using the SCADA system. This journal simulates a SCADA system for the coagulation process in water treatment installations. The main base of the SCADA system is the Schneider M221 PLC and the Weintek MT8071iP HMI

Improving conventional household greensand treatment for efficient Mn(II) removal from drinking water

Geogenic contaminants pose a global threat to ensuring access to safe drinking water. Manganese (Mn) is a naturally-occurring redox-active element which in its reduced form, Mn(II), is a widespread groundwater contaminant. Prolonged consumption of water containing high levels of Mn has been linked to adverse effects on memory, attention, motor skills, and nervous system function, particularly in vulnerable groups including pregnant individuals and young children. In addition, Mn can lead to aesthetic issues such as altered taste, clogging, and damage to plumbing systems. While Mn has historically been regulated as an aesthetic concern, a mounting body of evidence linking health issues to Mn exposure through drinking water has heightened the challenges of using groundwater to meet drinking water needs. Recently, Health Canada established a health guideline which set a maximum acceptable concentration for total Mn in drinking water of 120 μg/L. Greensand (GS) filters are commonly used in conventional drinking water treatment systems for Mn(II) removal due to their cost-effectiveness and high exchange capacity. However, under certain conditions conventional GS systems may have a low Mn(II) removal efficiency (Galangashi et al. 2021) and encounter challenges related to Mn leaching (Outram et al. 2018), resulting in failure to meet health-related standards. Furthermore, GS filters typically undergo regeneration using potassium permanganate (KMnO4), a mild oxidant that results in the release of additional Mn waste byproducts during the regeneration of the filter. Recent research suggests that Mn-containing materials can effectively activate peroxymonosulfate (PMS) and produce reactive oxygen species (ROS) that facilitate contaminant degradation. This study aims to investigate whether PMS may be used to improve greensand treatment systems and enhance Mn(II) removal from drinking water. Batch experiments were performed to test the Mn(II) removal efficiency across a range of PMS concentrations (0-500 μM) and GS mass (0.1-3 g). Aqueous Mn concentrations were measured over time using inductively coupled plasma optical emission spectrometry (ICP-OES). Solid-phase reaction products were characterized by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The mechanisms of Mn oxidation were identified by quenching experiments and electron paramagnetic resonance (EPR) spectroscopy. The activation of PMS by greensand significantly increased the removal efficiency of Mn(II) compared to the conventional method (e.g., 96.83(±3.77)% at PMS = 500 µM vs. 5.77(±11.1)% at PMS = 0 µM). Our results attribute the mechanism underlying increased Mn removal in our improved treatment method to advanced oxidation processes that involve free radicals (e.g., hydroxyl radical (·OH) and sulfate radical (SO4·-)) and non-free radical pathways, with Mn oxides as the main oxidation products. This study provides a new treatment method for more efficient Mn(II) removal while simultaneously reducing Mn wastes produced during the regeneration cycle which allows for a more sustainable and holistic management of invaluable groundwater resources.

Adsorption of Phenoxyacetic Herbicides from Water on Carbonaceous and Non-Carbonaceous Adsorbents.

The increasing consumption of phenoxyacetic acid-derived herbicides is becoming a major public health and environmental concern, posing a serious challenge to existing conventional water treatment systems. Among the various physicochemical and biological purification processes, adsorption is considered one of the most efficient and popular techniques due to its high removal efficiency, ease of operation, and cost effectiveness. This review article provides extensive literature information on the adsorption of phenoxyacetic herbicides by various adsorbents. The purpose of this article is to organize the scattered information on the currently used adsorbents for herbicide removal from the water, such as activated carbons, carbon and silica adsorbents, metal oxides, and numerous natural and industrial waste materials known as low-cost adsorbents. The adsorption capacity of these adsorbents was compared for the two most popular phenoxyacetic herbicides, 2,4-dichlorophenoxyacetic acid (2,4-D) and 2-methyl-4-chlorophenoxyacetic acid (MCPA). The application of various kinetic models and adsorption isotherms in describing the removal of these herbicides by the adsorbents was also presented and discussed. At the beginning of this review paper, the most important information on phenoxyacetic herbicides has been collected, including their classification, physicochemical properties, and occurrence in the environment.

Long-Term Nitrogen and Phosphorus Outflow from an Instream Constructed Wetland under Precipitation Variability

In many agricultural watersheds, surface runoff often causes unwanted nitrogen (N) and phosphorus (P) losses from croplands into stream networks. When this phenomenon is pronounced, it significantly changes N and P concentrations in streams affecting aquatic ecosystems. To protect stream water quality, the installation of instream-constructed wetlands (ICWs) for treating runoff water is often reported as a low-cost alternative to conventional water treatment systems. Indeed, ICWs have the capacity to collect and temporarily retain nutrients transported from agricultural landscapes and then slowly release them into downstream networks. However, the long-term hydrologic behavior of ICWs relative to N and P outflow control is still insufficiently reported. Especially in the context of climate change, it is relevant to investigate the effect of precipitation variability on ICWs N and P outflow. This study uses the soil and water assessment tool (SWAT) model to approximate the long-term hydrologic behavior of an experimental ICW installed in a small agricultural watershed. The model was set assuming a continuous corn and soybean rotation on croplands, then a multidecadal (period 2001–2020) simulation was used to evaluate the implication of precipitation variability on total nitrogen (TN), nitrate-N (NO3-N), total P (TP), and dissolved P (DP) outflows. Results show meaningful changes in the precipitation pattern with contrasting effects on N and P outflows. While analyses show significant trends in the maximum monthly precipitation, nutrient outflows during two consecutive decades, 2001–2010 and 2011–2020, show increases of 46% for TN, and 82% for TP. At the watershed scale, month-to- month TN and TP outflows range from 24 to 810 kg N and 26 to 1358 kg P during 2011–2020, compared with 42 to 398 kg N and 40 to 566 kg P during 2001–2010. The increase in nutrient outflow is particularly pronounced for TP and DP which show significant trends and high correlations (r > 0.70) with maximum monthly precipitation. An exception is nitrate-N outflow, which counts on average for less than 5% of TN outflow but appears more affected by the timing of N fertilization in the watershed.

Seasonal and Spatial Variations in the Presence of Giardia and Cryptosporidium in Rural Drinking Water Supply Systems in Different Municipalities of Antioquia, Colombia

This study evaluated the seasonal and spatial variations in the presence of Giardia and Cryptosporidium in rural drinking water supply systems of different municipalities of Antioquia. The municipalities evaluated were Envigado, Caldas, Sabaneta, La Estrella, Itagüi, Bello, Barbosa, Copacabana, and Girardota, located in the department of Antioquia, Colombia. The experimentation was carried out over 9 sampling campaigns in the period between July 2019 and November 2020. This period encompassed the two seasons presented in Colombia: dry and wet. Each municipality included in this study has a conventional basic drinking water treatment system (DWTS) which includes sand trap, rapid filtration, and chlorination. The results showed good removal efficiencies of Cryptosporidium and Giardia in the DWTS evaluated. However, evaluation of other characteristics of water quality and of the water quality risk index for human consumption (IRCA) showed concerning water quality conditions in the rural drinking water systems supply. The prevailing risk levels of the drinking water are medium, high, or non-viable sanitary, which means the population is supplied with water that does not meet the minimum quality criteria established by Colombian regulations.

Fouling in the membrane distillation treating superficial water with phenolic compounds

The production of drinking water free of micropollutants is a challenge that has currently received a lot of attention. Micropollutants, such as phenolic compounds, are not removed from conventional water treatment systems and may occur in drinking water. The removal of these compounds in the quest to achieve sustainable water management makes advanced technologies, such as membrane distillation, important. However, the long-term use of membrane distillation is restricted by membrane fouling, while how this process behaves towards micropollutant removal has been unanswered. In this regard, this study aims to evaluate the impact of fouling in the direct contact membrane distillation on the rejection of 15 phenolic compounds in surface water. According to the results, the process achieved a recovery rate of 93.26%, without compromising the permeate quality. Fouling was mainly attributed to organic elements from surface water, particularly those with sizes ranging from 1.143 to 1.214 µm that were comparable to bacteria. The fouling layer formed favored the concentration of the phenolic compound in the feed solution with practically no mass loss in the process. The average removals of phenolic compounds varied from 94.30 ± 1.93% to 99.24 ± 0.24%. Thus, although fouling occurred, membrane distillation was robust in phenolic compounds retention and produced high-quality water.

Synthesis of a granular composite based on polyvinyl alcohol-Fe:Ce bimetallic oxide particles for the selective adsorption of As(V) from water

In this study, Fe:Ce bimetallic oxide particles (BOP) were immobilized in poly(vinyl) alcohol (PVA) hydrogel, aiming to engineer a granular material that preserves the adsorptive properties of BOP powder, allowing their use in conventional water treatment systems. Through a detailed evaluation of the synthesis conditions, we were able to produce a composite (PVA/BOP) with excellent physicochemical properties, while retaining up to 100% of the BOP arsenic adsorption capacity, even at ppb of As(V) concentrations. The composites were characterized by SEM, N2 physisorption, FT-IR, potentiometric titration, and compression test. Also, adsorption experiments including isotherms, kinetics, pH effect and selectivity were performed. The inclusion of BOP in the PVA hydrogel improved the mechanical properties of the hydrogel, increasing the elastic limit from 60% for PVA to 90% for the composite, making it suitable for packed bed systems. The BOP particles showed a uniform dispersion in the composite as evidenced by SEM. The surface area of the composite reached 10 m2/g and has an acidic surface (pHpzc of 4.1). The FTIR analyses allowed us to demonstrate the interactions of BOP with PVA, and to propose the arsenic adsorption mechanism. The dry composite labeled as C7P60 showed excellent arsenic removal: adsorption capacity of 77.62 mg/g measured at 0.8 mg As/L and pH 7; adsorption kinetics of 1.69 mg As(V)/min·g reaching equilibrium in less than 30 min; and a high affinity for arsenic in presence of competing anions, including F−, Cl−, HCO3−, NO3−, SO42− and H2PO4−. The results reported herein suggest that this granular composite PVA/BOP can be an excellent candidate to address arsenic water contamination problems.

A Review on the Use of Membrane Technology Systems in Developing Countries.

Fulfilling the demand of clean potable water to the general public has long been a challenging task in most developing countries due to various reasons. Large-scale membrane water treatment systems have proven to be successful in many advanced countries in the past two decades. This paves the way for developing countries to study the feasibility and adopt the utilization of membrane technology in water treatment. There are still many challenges to overcome, particularly on the much higher capital and operational cost of membrane technology compared to the conventional water treatment system. This review aims to delve into the progress of membrane technology for water treatment systems, particularly in developing countries. It first concentrates on membrane classification and its application in water treatment, including membrane technology progress for large-scale water treatment systems. Then, the fouling issue and ways to mitigate the fouling will be discussed. The feasibility of membrane technologies in developing countries was then evaluated, followed by a discussion on the challenges and opportunities of the membrane technology implementation. Finally, the current trend of membrane research was highlighted to address future perspectives of the membrane technologies for clean water production.

In-situ sequestration of perfluoroalkyl substances using polymer-stabilized ion exchange resin

Remediation of groundwater impacted by per- and polyfluoroalkyl substances (PFAS) is challenging due to the strength of the carbon-fluorine bond and the need to achieve nanogram per liter drinking water targets. Previous studies have shown that ion exchange resins can serve as effective sorbents for the removal of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS) in conventional water treatment systems. The objectives of this study were to evaluate the in situ delivery and PFAS sorption capacity of a polymer-stabilized ion exchange resin (S-IXR) consisting of Amberlite® IRA910 beads and Pluronic® F-127 in a quartz sand. At concentrations below 100 µg/L, individual and mixed PFAS adsorption on resin beads exhibited linear isotherms with no apparent competitive effects. However, at concentrations up to 100 mg/L, PFAS adsorption isotherms were non-linear and a mixture of six PFAS exhibited strong competitive effects. In columns packed with 40–50 mesh Ottawa sand, injection of the S-IXR suspension created a uniform sorptive zone that increased PFOA or PFOS retention by more than five orders-of-magnitude compared to untreated control columns. Multi-solute column studies revealed earlier breakthrough of shorter-chain length PFAS, which was consistent with the mixed PFAS adsorption data. These findings indicate that injectable ion exchange resins could provide an effective in situ remediation strategy for PFAS-impacted groundwater plumes.

Water Treatment in Hybrid Connection of Coagulation, Ozonation, UV Irradiation and Adsorption Processes

In recent years, conventional water treatment systems have been supported by ozonation or UV irradiation processes. The efficiency of four hybrid processes: (1) coagulation and adsorption, (2) ozonation and coagulation, (3) ozonation, coagulation and adsorption, (4) ozonation, UV irradiation, coagulation and adsorption of inorganic and organic pollutants removal was analysed. In the presented study, the content of organic matter in natural water was evaluated as colour, oxidisability (OXI), total and dissolved organic carbon (TOC and DOC) content and UV absorbance at the wavelength of 254 nm for natural and modified water. Additionally, removal of Ni2+, Cd2+and Pb2+ ions during the treatment processes was analysed. The coagulation process with the use of polyaluminium chloride removed 45% of colour and 39, 26% and 45% of OXI, TOC and UV absorbance, respectively. Using the ozonation before coagulation increased efficiency of colour and UV254 absorbance reduction by 33% and 25%, respectively. Coagulation with both UV irradiation and adsorption had insignificant results on the analysed factors value. The coagulation process was the most efficient for metal ions removal (40–78%). The ozonation process before coagulation increased removal up to 55–85%. Additional irradiation with UV or using of the adsorbent during coagulation of initially ozonated water had an insignificant impact on metal ions concentration in water.

Non-thermal plasma-based inactivation of bacteria in water using a microfluidic reactor

Failure of conventional water treatment systems may lead to the contamination of water sources, which can cause outbreaks of waterborne healthcare associated infections. Advanced oxidation processing by non-thermal plasma has the potential to treat water without the addition of chemicals. Antibiotic resistant Pseudomonas aeruginosa and Escherichia coli were chosen to investigate the use of non-thermal plasma generated in a microfluidic reactor to disinfect bacteria contaminated water. The microfluidic reactor used in this study utilized a dielectric barrier discharge, in a gas-liquid phase annular flow regime. Microbiological analysis of water inoculated with P. aeruginosa and E. coli was carried out before and after plasma treatment. Using air as the carrier gas, effective disinfection of water was achieved. At the lowest flow rate (35 µL/min), P. aeruginosa and E. coli viability were drastically reduced, with an approximate 8 log maximum decrease in viability following an estimated residence time of 5 s of plasma treatment. Scanning electron microscopy indicated changes in cell morphology due to the plasma treatment. Live/Dead assays revealed that the membranes of the cells had been damaged after plasma treatment. This work demonstrated that non-thermal plasma has the potential to disinfect against microbial contamination in water.

Piloting During a Pandemic

Key TakeawaysFour pilot teams shared experiences with piloting during the COVID‐19 pandemic, emphasizing that thoughtful planning streamlines the piloting process while mitigating the risk of transmitting illness.Remote access to and control of pilot equipment, along with the use of virtual communication platforms, enabled teams to successfully perform pilot‐scale studies.Operating pilot systems through the pandemic allowed teams to respond to drastic changes on a small scale to mitigate risks around full‐scale processes at the treatment plant.

Evaluation of Moringa oleifera Extract as a Biocoagulant to Remove Microcystis aeruginosa Cells and Dissolved Metabolites

Cyanobacteria are microorganisms capable of releasing toxic metabolites in freshwater, deleterious to humans and other living organisms even in very low concentrations. Removing both cyanobacteria cells and their metabolites in conventional water treatment systems is still a challenge that needs to be addressed. This paper evaluated the use of Moringa oleifera saline extract and polyaluminum chloride (PACl) as coagulants in order to remove cells and metabolites of M. aeruginosa from water. Samples consisted of synthetic water spiked with humic acid and M. aeruginosa cells, with a final turbidity of 25 NTU. Coagulation/flocculation/dissolved air flotation (C/D/DAF) tests were performed with 50 mg/L of M. oleifera coagulant, combined with different proportions of PACl (10–50%). For removal of metabolites, 25 μg/L of microcystin and 50 ng/L of 2-MIB and geosmin were spiked in water samples. The best results were obtained with 70:30 M. oleifera:PACl, achieving removal efficiencies of 81.37%, 74.69%, and 71.06% for turbidity, color, and cell density, respectively. For microcystin, 2-MIB, and geosmin, after filtration (30 min), global removal efficiencies (clarification + filtration) of 99.45%, 62.37%, and 100%, respectively, were obtained, using Sand+GAC filter. The results suggest that the substitution of PACl by M. oleifera extract can be a good option to remove cyanobacteria cells from water, and high removal efficiencies of metabolites can be achieved after the complete proposed treatment.

Ecological and health risk assessment of polycyclic aromatic hydrocarbons (PAHs) in Sungai Perak, Malaysia

Polycyclic aromatic hydrocarbons (PAHs) are mutagenic and bio-accumulates in nature. This research aims to determine the ecological and health risk assessment of PAHs in Sungai Perak, Malaysia. The sampling was conducted at the up and downstream of Sungai Perak in the district of Perak Tengah, Malaysia. The sampling stations were Tanjung Belanja Bridge (TBB), Water Treatment Plant Parit (WTPP), Parit Town Discharge (PTD), Water Treatment Plant Senin (WTPS) and Water Treatment Plant Kepayang (WTPK). The water treatment plants channel water through the distribution network, to Manjung (249,600 people), Perak Tengah (249,600 people), Kinta (810,400 people) and Hilir Perak (144,400 people) districts. The hazard quotient (HQ) and hazard index (HI) were applied for ecological and health risk assessments. The lifetime cancer risk (LCR) was employed for the health risk assessment. The PAHs contamination level presumptions for all sampling campaigns were low (0–100 μg/L). The HI values of ecological and health risk assessments were found to be aligned with each other. The HI values for raw water were below one (<1) indicating low or no risk while the treated water HI values were more than one (>1) indicating to high risk to aquatic organisms and human health. However, the LCR for raw and treated water exceeded the maximum permissible limit, 1.0 × 10−6 equals to cancer risk of 1 in 1,000,000 people. The LCR for raw water were 1.71 × 10−4 (TBB), 1.35 × 10−4 (WTPP), 1.43 × 10−4 (PTD), 9.54 × 10−5 (WTPS) and 2.37 × 10−4 (WTPK). Meanwhile, the LCR for treated water were 6.90 × 10−5 (WTPP), 5.42 × 10−5 (WTPS) and 2.63 × 10−4 (WTPK). The conventional water treatment system appears to be inefficient to remove PAHs, risking the security of public health. Thus, restructuring the infrastructure of water treatment plants or considering an alternative to rivers as domestic water sources are highly recommended.

Graphene-Based Composites as Catalysts for the Degradation of Pharmaceuticals.

The incessant release of pharmaceuticals into the aquatic environment continues to be a subject of increasing concern. This is because of the growing demand for potable water sources and the potential health hazards which these pollutants pose to aquatic animals and humans. The inability of conventional water treatment systems to remove these compounds creates the need for new treatment systems in order to deal with these class of compounds. This review focuses on advanced oxidation processes that employ graphene-based composites as catalysts for the degradation of pharmaceuticals. These composites have been identified to possess enhanced catalytic activity due to increased surface area and reduced charge carrier recombination. The techniques employed in synthesizing these composites have been explored and five different advanced oxidation processes—direct degradation process, chemical oxidation process, photocatalysis, electrocatalyis processes and sonocatalytic/sono-photocatalytic processes—have been studied in terms of their enhanced catalytic activity. Finally, a comparative analysis of the processes that employ graphene-based composites was done in terms of process efficiency, reaction rate, mineralization efficiency and time required to achieve 90% degradation.

Per and polyfluoroalkyl substances scientific literature review: water exposure, impact on human health, and implications for regulatory reform.

Among other emerging contaminants in water, per and polyfluoroalkyl substances (PFASs) have garnered international attention from the scientific community on a global scale. Some countries, such as the United States, have found that PFASs are present in humans on a wide scale. Although two PFASs have been widely studied-Perfluorooctanoic acid and Perfluorooctanesulfonic acid-many more PFASs are being created by industry andare either not known, not studied, or both. The objective of this literature review on PFASs is to give an overview of the information available about PFASs related to human exposure. The information from this literature review on the exposure of humans to PFASs through drinking water and the lack of many conventional drinking water treatment systems' ability to remove PFASs (particularly short-chain PFASs) suggests that current regulatory limits are insufficient to adequately protect humans. This is especially true for particularly vulnerable populations such as infants, young children, and developing children (pubescent). The gaps in the current knowledge and in current regulatory approaches could have long-term effects on human health.

Bibliometric approach to the perspectives and challenges of membrane separation processes to remove emerging contaminants from water.

The presence of contaminants in water is concerning due to the potential impacts on human health and the environment, and ingested contaminants cause harm in various ways. The conventional water treatment systems are not efficient to remove these contaminants. Therefore, novel techniques and materials for the removal of contaminants are increasingly being developed. The separation process using modified membranes can remove these micropollutants; therefore, they have attracted significant research attention. Among the materials used for manufacturing of these membranes, composites based on graphene oxide and reduced graphene oxide are preferred owing to their promising properties, such as mechanical resistance, thermal and chemical stability, antifouling capacity, water permeability, high thermal and electrical conductivity, high optical transmittance and high surface area. Membrane separation processes (MSP) can be used as secondary or tertiary treatment during the supply of wastewater. However, the efficient and accessible applications of these technologies are challenging. This study aims to demonstrate the main concepts of membrane separation processes and their application in the removal of emerging contaminants. This study reports bibliometric mapping, relevant data on studies using membranes as water treatment processes, and their viability in industrial applications. The main challenges and perspectives of these technologies are discussed in detail as well.

In Situ Sequestration of Perfluoroalkyl Substances Using Polymer-Stabilized Powdered Activated Carbon.

Remediation of groundwater impacted by per- and polyfluoroalkyl substances (PFAS) is particularly challenging due to the resistance of the molecule to oxidation because of the strength of the carbon-fluorine bond and the need to achieve low nanogram per liter drinking water targets. Previous studies have shown that activated carbon is an effective sorbent for removal of perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS) in conventional water treatment systems. The objective of this study was to evaluate the in situ delivery and sorptive capacity of an aqueous suspension containing powdered activated carbon (PAC) stabilized with polydiallyldimethylammonium chloride (polyDADMAC). Batch reactor studies demonstrated substantial adsorption of PFOA and PFOS by polyDADMAC-stabilized PAC, which yielded Freundlich adsorption coefficients of 156 and 629 L/g-n, respectively. In columns packed with 40-50 mesh Ottawa sand, injection of a PAC (1000 mg/L) + polyDADMAC (5000 mg/L) suspension created a sorptive region that increased subsequent PFOA and PFOS retention by 3 orders of magnitude relative to untreated control columns, consistent with the mass of retained PAC. Experiments conducted in a heterogeneous aquifer cell further demonstrated the potential for stabilized-PAC to be an effective in situ treatment option for PFAS-impacted groundwater.