A critical review of the mechanisms, factors, and performance of pervious concrete to remove contaminants from stormwater runoff.

Stormwater can carry pollutants accumulated on impervious surfaces in urban areas into natural water bodies in absence of stormwater quality improvement devices. Pervious concrete (PC) pavement is one of the low-impact development practices introduced for urban flooding prevention and stormwater pollution reduction. PC removes various types of water contaminants. Mechanisms contributing to the water pollution removal capacity of PC can be categorized into three groups: physical, chemical, and biological. Properties of PC such as permeability, porosity, thickness, and adsorption capacity influence removal of all contaminants, although their impact might differ depending on the pollutant properties. Chemical mechanisms include precipitation, co-precipitation, ion and ligand exchange, complexation, diffusion, and sorption. Bulk organics and nutrients are removed primarily by biodegradation. Physical filtration is the primary mechanism to retain suspended solids, although biological activities may have a minor contribution. Release of calcium (Ca2+) and hydroxide (OH-) from hardened cement elevates the effluent pH, which is an environmental concern. However, the pH elevation is also the prime contributor to heavy metals and nutrients removal through precipitation. Specific cementitious materials (e.g., Pozzolans and nanoparticles) and carbonation curing approach are recommended to control effluent pH elevation. Complexation, diffusion, ion solubility, and stability constants are other mechanisms and parameters that influence heavy metal removal. Organic matter availability, electrostatic attraction, temperature, pH, contact time, specific surface area, and roughness of PC pores contribute to the pathogen removal process. Although PC has been found promising in removing various water pollutants, limited salinity removal can be achieved due to the inherent release of Ca2+and OH- from PC.

Elucidating the performance of UV-based photochemical processes for the removal of trace organic contaminants: Degradation and toxicity evaluation.

In this study, the performance of standalone ultraviolet (UV) photolysis and UV-based advanced oxidation processes (AOPs), namely, UV/hydrogen peroxide, UV/chlorine, UV/persulphate, and UV/permonosulphate, were investigated for the degradation of 31 trace organic contaminants (TrOCs). Under the tested conditions, standalone UV photolysis did not achieve effective removal of TrOCs. To improve the degradation efficiency of UV photolysis, four different oxidants were added individually to the test solution. The effect of these oxidants in the absence of UV irradiation was also explored and only chlorine showed promising degradation of some contaminants. During the chlorination of 31 investigated TrOCs, only six demonstrated greater than 50% degradation. The combined UV-based AOPs demonstrated much improved degradation (ranging from 65 to 100%) depending on TrOC-structure and oxidant concentration. The UV/hydrogen peroxide process showed similar degradation of TrOCs, irrespective of the functional groups (i.e., electron withdrawing groups, EWGs and electron donating groups, EDGs) present in their structures. Conversely, the UV/sulphate and UV/chlorine based processes achieved better degradation of the TrOCs with EDGs in their structures. TrOCs degradation improved up to 40% when oxidants concentrations were increased from 0.1 to 1 mM, and further increasing the concentration to 2 mM did not improve degradation. Toxicity evaluation using bioluminescence test (BLT assay) demonstrated that except for UV/hydrogen peroxide, all UV-based AOPs increased the toxicity of the treated effluent, indicating generation of toxic by-products. This study elucidates the performance of four different UV-based AOPs for the removal of commonly detected diverse TrOCs for the first time.

Microplastics as an emerging contaminant of concern to our environment: a brief overview of the sources and implications.

Over the years, it has become evident that microplastics are one of the most important contaminants of concern requiring significant attention. The large abundance of microplastics that are currently in the environment poses potential toxicity risks to all organisms that are exposed to them. Microplastics have been found to affect the physiological and biological processes in marine and terrestrial organisms. As well as being a contaminant of concern in itself, microplastics also have the ability to act as vectors for other contaminants. The potential for microplastics to carry pollutants and transfer them to other organisms has been documented in the literature. Microplastics have also been linked to hosting antibiotic resistant bacteria and antibiotic resistance genes which poses a significant risk to the current health system. There has been a significant increase in research published surrounding the topic of microplastics over the last 5 years. As such, it is difficult to determine and find up to date and relevant information. This overview paper aims to provide a snapshot of the current and emerging sources of microplastics, how microplastics can act as a contaminant and have toxic effects on a range of organisms and also be a vector for a large variety of other contaminants of concern. The aim of this paper is to act as a tool for future research to reference relevant and recent literature in this field.

Evaluating the generation of microplastics from an unlikely source: The unintentional consequence of the current plastic recycling process.

This study casts light on the potential of microplastic generation during plastic recycling - an unintended consequence of the process. To date, microplastics have been detected in the wastewater and sludge from plastic recycling facilities; however, generation pathways, factors and minimisation strategies are understudied. The purpose of this study is to identify the factors affecting microplastic generation, namely, plastic type and weathering conditions. The size reduction phase, which involved the mechanical shredding of the plastic waste material, was identified to be the predominate source of microplastic generation. Material type was found to significantly affect microplastic generation rates. Focussing on the microplastic particles in the size range of 0.212-1.18 mm, polycarbonate (PC), polyethylene terephthalate (PET), polypropylene (PP), and high-density polyethylene (HDPE) generated 28,600 ± 3961, 21,093 ± 2211, 18,987 ± 752 and 6807 ± 393 particles/kg of plastic material shredded, respectively. The significant variations between different plastic types were correlated (R2 = 0.88) to the hardness of the plastic. Environmental weathering was observed to significantly affect microplastic generation rates. Generation rates increased for PC, PET, PP, and HDPE by 185.05 %, 159.80 %, 123.70 % and 121.74 %, respectively, over a six-month environmental exposure period. The results in this study confirm production of large amounts of microplastics from the plastic recycling industry through its operational processes, which may be a significant source for microplastic pollution if measures to reduce their production and removal from wastewater and sludge are not considered.

Responses of syntrophic microbial communities and their interactions with polystyrene nanoplastics in a microbial electrolysis cell.

Microbial electrochemical technologies are promising for simultaneous energy recovery and wastewater treatment. Although the inhibitory effects of emerging pollutants, particularly micro/nanoplastics (MPs/NPs), on conventional wastewater systems have been extensively studied, the current understanding of their impact on microbial electrochemical systems is still quite limited. Microplastics are plastic particles ranging from 1 µm to 5 mm. However, nanoplastics are smaller plastic particles ranging from 1 to 100 nm. Due to their smaller size and greater surface area, they can penetrate deeper into biofilm structures and cell membranes, potentially disrupting their integrity and leading to changes in biofilm composition and function. This study first reports the impact of polystyrene nanoplastics (PsNPs) on syntrophic anode microbial communities in a microbial electrolysis cell. Low concentrations of PsNPs (50 and 250 µg/L) had a minimal impact on current density and hydrogen production. However, 500 µg/L of PsNPs decreased the maximum current density and specific hydrogen production rate by ∼43 % and ∼48 %, respectively. Exposure to PsNPs increased extracellular polymeric substance (EPS) levels, with a higher ratio of carbohydrates to proteins, suggesting a potential defense mechanism through EPS secretion. The downregulation of genes associated with extracellular electron transfer was observed at 500 µg/L of PsNPs. Furthermore, the detrimental impact of 500 µg/L PsNPs on the microbiome was evident from the decrease in 16S rRNA gene copies, microbial diversity, richness, and relative abundances of key electroactive and fermentative bacteria. For the first time, this study presents the inhibitory threshold of any NPs on syntrophic electroactive biofilms within a microbial electrochemical system.

Dysregulated NAD(H) homeostasis associated with ciprofloxacin tolerance in Escherichia coli investigated on a single-cell level with the Peredox [NADH:NAD+] biosensor.

Introduction: Antibiotic persistence (subpopulation tolerance) occurs when a subpopulation of antibiotic sensitive cells survives prolonged exposure to a bactericidal concentration of an antibiotic, and is capable of regrowth once the antibiotic is removed. This phenomenon has been shown to contribute to prolonged treatment duration, infection recurrence, and accelerated development of genetic resistance. Currently, there are no biomarkers which would allow for segregation of these antibiotic-tolerant cells from the bulk population prior to antibiotic exposure, limiting research on this phenomenon to retrograde analyses. However, it has been previously shown that persisters often have a dysregulated intracellular redox homeostasis, warranting its investigation as a potential marker for antibiotic tolerance. Furthermore, it is currently unknown whether another antibiotic tolerant subpopulation - viable but non-culturable cells (VBNCs), are simply persisters with extreme lag phase, or are formed through separate pathways. VBNCs similarly to persisters remain viable following antibiotic exposure, however, are not capable of regrowth in standard conditions. Methods: In this article we employed an NADH:NAD+ biosensor (Peredox) to investigate NADH homeostasis of ciprofloxacin-tolerant E. coli cells on a single-cell level. [NADH:NAD+] was used as a proxy for measuring intracellular redox homeostasis and respiration rate. Results and Discussion: First, we demonstrated that ciprofloxacin exposure results in a high number of VBNCs, several orders of magnitude higher than persisters. However, we found no correlation in the frequencies of persister and VBNC subpopulations. Ciprofloxacin-tolerant cells (persisters & VBNCs) were actively undergoing respiration, although at a significantly lower rate on average when compared to the bulk population. We also noted significant heterogeneity on a single-cell level within the subpopulations, however were unable to segregate persisters from VBNCs based on these observations alone. Finally, we showed that in the highly-persistent strain of E. coli, E. coli HipQ, ciprofloxacin-tolerant cells have a significantly lower [NADH:NAD+] ratio than tolerant cells of its parental strain, providing further link between disturbed NADH homeostasis and antibiotic tolerance.

Change in the chemical, mechanical and physical properties of plastics due to UVA degradation in different water matrices: A study on the recyclability of littered plastics.

To move towards a circular society, the recyclability potential of littered plastics should be explored to provide potential value for a product that is typically destined for landfill or incineration. This study aims to understand the changes in physical, mechanical, and chemical properties of four types of plastics (polyethylene terephthalate (PET), polypropylene (PP), polycarbonate (PC) and polylactic acid (PLA) after simulated environmental degradation. Plastic samples were subjected to different water matrices (in an attempt to simulate terrestrial, ocean, and river environments) to understand the role the environment plays on plastic degradation. Significant physical, mechanical, and chemical changes were observed for the PET, PP and PLA samples. Flakes and cracks were noted during the scanning electron microscopy (SEM) analysis of PET, PP and PLA illustrating the surface degradation that had occurred. Colour scanning of the samples provided complementary information about their suitability for upcycling or downcycling. Both PET and PP had visual colour changes, making them unsuitable for upcycling purposes. PLA had a significant decrease in its tensile strength in all environmental conditions, alongside significant chemical and surface change as revealed by Fourier-transform infrared (FTIR) and SEM analysis, respectively. PC had little to no changes in its chemical, mechanical, and physical properties due to high resistance to solar (UVA) degradation in presence of salt and natural organic matter in the form of humic acid. Therefore, out of the four types of plastics tested, PC was the only plastic determined to have good upcycling potential if collected from the environment. However, PET and PP could still be recycled into lower value products (i.e., construction materials).

Antibiotic sorption onto microplastics in water: A critical review of the factors, mechanisms and implications.

Microplastics as vectors for contaminants in the environment is becoming a topic of public interest. Microplastics have been found to actively adsorb heavy metals, per-fluorinated alkyl substances (PFAS), polychlorinated biphenyls (PCBs), polyaromatic hydrocarbons (PAHs), pharmaceuticals and personal care products (PPCPs) and polybrominated diethers (PBDs) onto their surface. Particular interest in microplastics capacity to adsorb antibiotics needs further attention due to the potential role this interaction plays on antibiotic resistance. Antibiotic sorption experiments have been documented in the literature, but the data has not yet been critically reviewed. This review aims to comprehensively assess the factors that affect antibiotic sorption onto microplastics. It is recognised that the physico- chemical properties of the polymers, the antibiotic chemical properties, and the properties of the solution all play a crucial role in the antibiotic sorption capacity of microplastics. Weathering of microplastics was found to increase the antibiotic sorption capacity by up to 171%. An increase in solution salinity was found to decrease the sorption of antibiotics onto microplastics, in some instances by 100%. pH also has a substantial effect on sorption capacity, illustrating the significance of electrostatic interactions on the sorption of antibiotics onto microplastics. The need for a uniform experimental design when testing antibiotic sorption is highlighted to remove inconsistencies in the data currently presented. Current literature examines the link between antibiotic sorption and antibiotic resistance, however, further studies are still required to fully understand this emerging global crisis.

A critical review of process parameters influencing the fate of antibiotic resistance genes in the anaerobic digestion of organic waste.

The overuse and inappropriate disposal of antibiotics raised severe public health risks worldwide. Specifically, the incomplete antibiotics metabolism in human and animal bodies contributes to the significant release of antibiotics into the natural ecosystems and the proliferation of antibiotic-resistant bacteria carrying antibiotic-resistant genes. Moreover, the organic feedstocks used for anaerobic digestion are often highly-rich in residual antibiotics and antibiotic-resistant genes. Hence, understanding their fate during anaerobic digestion has become a significant research focus recently. Previous studies demonstrated that various process parameters could considerably influence the propagation of the antibiotic-resistant genes during anaerobic digestion and their transmission via land application of digestate. This review article scrutinizes the influences of process parameters on antibiotic-resistant genes propagation in anaerobic digestion and the inherent fundamentals behind their effects. Based on the literature review, critical research gaps and challenges are summarized to guide the prospects for future studies.

Identification, classification and quantification of microplastics in road dust and stormwater.

Microplastics (MP) have become a major emerging class of pollutants representing significant eco-toxicological risks for ecosystems and marine environments. The aim of this study was to identify, classify and quantify MP present in both road dust and stormwater samples. A significantly higher level of MPs within road dust samples was detected from industrial area (1130 particles/kg of dust) than from residential area (520 particles/kg of dust), while stormwater samples from industrial and residential sites yielded 26 particles/L and 17 particles/L, respectively. Fiber-like shape accounted for 53% and 74% in road dust and stormwater samples, respectively. The main polymeric materials collected for both road dust and stormwater samples were, in order of occurrence (i) low-density polyethylene, (ii) high-density polyethylene, (iii) polypropylene, (iv) polyethylene terephthalate, (v) polystyrene, (vi) polyester and (vii) poly (amide). Most of the MP had an average maximum dimension smaller than 2 mm for both road dust and stormwater samples. The results from this study demonstrates that road dust is a significant contributor to MP pollution through direct polymeric materials wear off and transfer through stormwater, which eventually will end up in open water ways and broader ecological niches.

Applications of Membranes for Sustainability.

Applications of membranes in water and wastewater treatment, desalination, as well as other purification processes, have become more widespread over the past few decades [...].

Acid mine drainage and sewage impacted groundwater treatment by membrane distillation: Organic micropollutant and metal removal and membrane fouling.

Groundwater is the dominant source of freshwater in many countries around the globe, and the deterioration in its quality by contaminants originating from anthropogenic sources raises serious concern. In this study, a scenario where groundwater is contaminated by acid mine drainage (AMD) from mining activities and/or sewage was envisaged, and the performance of a direct contact membrane distillation (DCMD) system was investigated comprehensively for different compositions of the AMD- and sewage-impacted groundwater. Regardless of the composition, MD membrane achieved 98-100% removal of metals and bulk organics, while the removal of the selected micropollutants ranged between 80 and 100%. Effective retention of contaminants by the MD led to their accumulation over time, which affected the hydraulic performance of the MD membrane by reducing the permeate flux by 29-76%. When persulfate (PS)-mediated oxidation process was integrated with the DCMD, degradation of bulk organics (50-71%) and micropollutants (50-100%) by PS reduced their accumulation. Characterisation of the fouling layer revealed the occurrence of membrane scaling that was mainly due to the deposition of iron oxide or oxyhydroxide precipitates. For an identical composition of the AMD- and sewage-impacted groundwater, flux decline was 10% less in PS-assisted DCMD as compared to that in the standalone DCMD. However, this did not prevent the formation of iron oxide scales on MD membrane during the operation of PS-assisted DCMD. This study demonstrates the long-term performance of a standalone and PS-assisted DCMD operated in continuous-flow mode to treat AMD- and sewage-impacted groundwater for the first time.

A review of mechanisms underlying the impacts of (nano)microplastics on anaerobic digestion.

The presence of (nano)microplastics in domestic wastewater and their subsequent release to the aquatic environment via the discharge of treated sewage has raised significant concerns. Previous studies have also identified their excessive accumulation in sewage sludge. Anaerobic digestion is one of the most used sludge stabilization methods in wastewater treatment plants. Therefore, understanding the potential effects of (nano)microplastics on anaerobic digestion has been receiving increasing attention from researchers. This article provides a comprehensive review of mechanisms underlying the impacts of (nano)microplastics on anaerobic digestion. Notably, this review covers mechanisms of inhibition/enhancement of anaerobic digestion by (nano)microplastics and their potential impacts on biochemical pathways, key enzymes, functional genes, and microbial communities investigated to date. Moreover, potential environmental risks of biosolids contaminated with (nano)microplastics were highlighted. Finally, knowledge gaps and future research needs were outlined. This review will guide more standardized studies in the future, covering both fundamental and engineering aspects.

Reduction of excess sludge production by membrane bioreactor coupled with anoxic side-stream reactors.

While cleaning wastewater, biological wastewater treatment processes such as membrane bioreactors (MBR) produce a significant amount of sludge that requires costly management. In the oxic-settling-anoxic (OSA) process, sludge is retained for a temporary period in side-stream reactors with low oxygen and substrate, and then it is recirculated to the main reactor. In this way, excess sludge production is reduced. We studied the influence of the rate of sludge exchange between MBR and side-stream anoxic reactors on sludge yield reduction within MBR. Two MBRs, namely, MBROSA and MBRcontrol, each coupled with separate external anoxic side-stream reactors, were run in parallel for 350 days. Unlike MBRcontrol, MBROSA had sludge exchange with the external reactors connected to it. During the investigation over a sludge interchange rate (SIR) range of 0-22%, an SIR of 11% achieved the highest sludge reduction (58%). Greater volatile solids destruction i.e., bacterial cell lysis and extracellular polymeric substance (EPS) destruction occurred at the SIR of 11%, which helped to achieve the highest sludge reduction. The enhanced volatile solids destruction was evident by the release of nutrients in the external anoxic reactors. It was confirmed that the sludge yield reduction was achieved without compromising the wastewater treatment quality, sludge settleability and hydraulic performance of the membrane in MBR.

A chronicle of SARS-CoV-2: Seasonality, environmental fate, transport, inactivation, and antiviral drug resistance.

In this review, we present the environmental perspectives of the viruses and antiviral drugs related to SARS-CoV-2. The present review paper discusses occurrence, fate, transport, susceptibility, and inactivation mechanisms of viruses in the environment as well as environmental occurrence and fate of antiviral drugs, and prospects (prevalence and occurrence) of antiviral drug resistance (both antiviral drug resistant viruses and antiviral resistance in the human). During winter, the number of viral disease cases and environmental occurrence of antiviral drug surge due to various biotic and abiotic factors such as transmission pathways, human behaviour, susceptibility, and immunity as well as cold climatic conditions. Adsorption and persistence critically determine the fate and transport of viruses in the environment. Inactivation and disinfection of virus include UV, alcohol, and other chemical-base methods but the susceptibility of virus against these methods varies. Wastewater treatment plants (WWTPs) are major reserviors of antiviral drugs and their metabolites and transformation products. Ecotoxicity of antiviral drug residues against aquatic organisms have been reported, however more threatening is the development of antiviral resistance, both in humans and in wild animal reservoirs. In particular, emergence of antiviral drug-resistant viruses via exposure of wild animals to high loads of antiviral residues during the current pandemic needs further evaluation.

Impact of Inorganic Ions and Organic Matter on the Removal of Trace Organic Contaminants by Combined Direct Contact Membrane Distillation-UV Photolysis.

This study investigated the degradation of five trace organic contaminants (TrOCs) by integrated direct contact membrane distillation (DCMD) and UV photolysis. Specifically, the influence of inorganic ions including halide, nitrate, and carbonate on the performance of the DCMD-UV process was evaluated. TrOC degradation improved in the presence of different concentrations (1-100 mM) of fluoride ion and chloride ion (1 mM). With a few exceptions, a major negative impact of iodide ion was observed on the removal of the investigated TrOCs. Of particular interest, nitrate ion significantly improved TrOC degradation, while bicarbonate ion exerted variable influence-from promoting to inhibiting impact-on TrOC degradation. The performance of DCMD-UV photolysis was also studied for TrOC degradation in the presence of natural organic matter, humic acid. Results indicated that at a concentration of 1 mg/L, humic acid improved the degradation of the phenolic contaminants (bisphenol A and oxybenzone) while it inhibited the degradation of the non-phenolic contaminants (sulfamethoxazole, carbamazepine, and diclofenac). Overall, our study reports the varying impact of different inorganic and organic ions present in natural water on the degradation of TrOCs by integrated DCMD-UV photolysis: the nature and extent of the impact of the ions depend on the type of TrOCs and the concentration of the interfering ions.

A critical review on advanced oxidation processes for the removal of trace organic contaminants: A voyage from individual to integrated processes.

Advanced oxidation processes (AOPs), such as photolysis, photocatalysis, ozonation, Fenton process, anodic oxidation, sonolysis, and wet air oxidation, have been investigated extensively for the removal of a wide range of trace organic contaminants (TrOCs). A standalone AOP may not achieve complete removal of a broad group of TrOCs. When combined, AOPs produce more hydroxyl radicals, thus performing better degradation of the TrOCs. A number of studies have reported significant improvement in TrOC degradation efficiency by using a combination of AOPs. This review briefly discusses the individual AOPs and their limitations towards the degradation of TrOCs containing different functional groups. It also classifies integrated AOPs and comprehensively explains their effectiveness for the degradation of a wide range of TrOCs. Integrated AOPs are categorized as UV irradiation based AOPs, ozonation/Fenton process-based AOPs, and electrochemical AOPs. Under appropriate conditions, combined AOPs not only initiate degradation but may also lead to complete mineralization. Various factors can affect the efficiency of integrated processes including water chemistry, the molecular structure of TrCOs, and ions co-occurring in water. For example, the presence of organic ions (e.g., humic acid and fulvic acid) and inorganic ions (e.g., halide, carbonate, and nitrate ions) in water can have a significant impact. In general, these ions either convert to high redox potential radicals upon collision with other reactive species and increase the reaction rates, or may act as radical scavengers and decrease the process efficiency.

Microbial electrochemical systems for hydrogen peroxide synthesis: Critical review of process optimization, prospective environmental applications, and challenges.

Hydrogen peroxide (H2O2) is an industrial chemical that has been widely adopted for various industrial applications, including water and wastewater treatment. Currently, the majority of H2O2 is being produced through the anthraquinone oxidation process, which is disadvantageous due to the requirement of toxic raw materials and high energy input. Recently, microbial electrochemical cells (MXCs), such as microbial fuel cells and microbial electrolysis cells, have demonstrated great potential for effective H2O2 production via cathodic oxygen-reduction reaction (ORR). Previous studies have specified key operational parameters for scaling-up of H2O2-producing MXCs, where improvements in production rate, conversion efficiency, product concentration and stability are attainable. Moreover, various systems have demonstrated their value proposition in the contaminant removal aspects through direct removal of various environmental pollutants, water disinfection, and many more. This review is intended to highlight promising ways of H2O2 production with MXCs and on-site environmental applications of bioelectrochemically-produced H2O2.

Extraction of strategically important elements from brines: Constraints and opportunities.

Strategically important elements are those that are vital to advanced manufacturing, low carbon technologies and other growing industries. Ongoing depletion and supply risks to these elements are a critical concern, and thus, recovery of these elements from low-grade ores and brines has generated significant interest worldwide. Among the strategically important elements, this paper focuses on rare earth elements (REEs), the platinum-group metals and lithium due to their wide application in the advanced industrial economics. We critically review the current methods such as precipitation, ion exchange and solvent extraction for extracting these elements from low-grade ores and brines and provide insight into the technical challenges to the practical realisation of metal extraction from these low-grade sources. The challenges include the low concentration of the target elements in brines and inadequate selectivity of the existing methods. This review also critically analyzes the potential applicability of an integrated clean water production and metal extraction process based on conventional pressure-driven membrane and emerging membrane technologies (e.g., membrane distillation). Such a process can first enrich the strategically important elements in solution for their subsequent recovery along with clean water production.