Photodegradation and photocatalysis of per- and polyfluoroalkyl substances (PFAS): A review of recent progress.

Per- and polyfluoroalkyl substances (PFAS) are oxidatively recalcitrant organic synthetic compounds. PFAS are an exceptional group of chemicals that have significant physical characteristics due to the presence of the most electronegative element (i.e., fluorine). PFAS persist in the environment, bioaccumulate, and have been linked to toxicological impacts. Epidemiological and toxicity studies have shown that PFAS pose environmental and health risks, requiring their complete elimination from the environment. Various separation technologies, including adsorption with activated carbon or ion exchange resin; nanofiltration; reverse osmosis; and destruction methods (e.g., sonolysis, thermally induced reduction, and photocatalytic dissociation) have been evaluated to remove PFAS from drinking water supplies. In this review, we will comprehensively summarize previous reports on the photodegradation of PFAS with a special focus on photocatalysis. Additionally, challenges associated with these approaches along with perspectives on the state-of-the-art approaches will be discussed. Finally, the photocatalytic defluorination mechanism of perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS) following complete mineralization will also be examined in detail.

Study of Legionella pneumophila treatment with copper in drinking water by single cell-ICP-MS.

Legionella pneumophila is a persistent opportunistic pathogen that poses a significant threat to domestic water systems. Previous studies suggest that copper (Cu) is an effective antimicrobial in water systems. A rapid and sensitive quantification method is desired to optimize the conditions of L. pneumophila treatment by Cu and to better understand the interaction mechanisms between Cu and cells. In this study, we developed a highly sensitive single cell (SC)-ICP-MS method to monitor L. pneumophila cell concentration and track their uptake of Cu. The SC-ICP-MS method showed excellent sensitivity (with a cell concentration detection limit of 1000 cells/mL), accuracy (good agreement with conventional hemocytometry method), and precision (relative standard deviation < 5%) in drinking water matrix. The cupric ions (Cu2+) treatment results indicated that the total L. pneumophila cell concentration, Cu mass per cell, colony-forming unit counting, and Cu concentration in supernatant all exhibited a dose-dependent trend, with 800-1200 µg/L reaching high disinfection rates in drinking water. The investigation of percentages of viable and culturable, viable but nonculturable (VBNC), and lysed cells suggested there always were VBNC present at any Cu concentration. Experimental results of different Cu2+ treatment times further suggested that L. pneumophila cells developed an antimicrobial resistant mechanism with the prolonged Cu exposure. This is the first quantification study on the interactions of Cu and L. pneumophila in drinking water using SC-ICP-MS.

Fragmentation and release of pristine and functionalized carbon nanotubes from epoxy-nanocomposites during accelerated weathering.

There is an increasing volume of nano-enabled materials in the market. Once composites containing nano-additives are disposed of, weathering could deteriorate their structures, releasing nanoparticles and risking exposure of humans and aquatic organisms. Composite degradation due to environmental aging continues, including structural deterioration resulting in cracking, fragmentation, and release of microplastics and nano-additives to the environment. This research aims to study the degradation and release of initially embedded nanomaterials (NMs) from composites and their toxicity. The molecular interaction of carbon nanotube (CNT)/polymer composites is critical for modifying the polymer properties. This study investigated the interactions of functional multiwalled carbon nanotube (MWCNT) composites which affect their release during accelerated weathering processes. Different epoxy-MWCNT composites were prepared by filling a polymer with pure MWCNTs and MWCNTs functionalized with acid (-COOH) and amine (-NH2) groups. The physical and chemical changes of aged composites were characterized by gravimetric analysis, contact angle measurements, FTIR, SEM, and laser confocal microscopy. A loss of hydrophobicity was observed for composite surfaces long before surface cracks materialized. Released polymer fragments and nanoparticles were analyzed in wash water using TEM, FTIR and Raman spectroscopy. The environmental risks for long-term use of CNT-polymer composites and the influence of fillers on the extent of chemical photodegradation depended on the combination of polymer and fillers. If nanoparticles are released from the matrix, the high surface-to-volume ratio and reactivity of NMs make them highly dynamic in environmental systems. Exposure to these released NMs could negatively affect human health and the environment. This study provides fragmentation and CNT particle release data that could describe how molecular-level interactions between functionalized CNTs and epoxy polymers affect the aging and release of CNTs. A toxicity assessment based on a reactive oxygen species (ROS) formation assay and MTS assay for cell viability and activity of the released polymer and CNT fragments and leachate showed moderate levels of cytotoxicity of released materials as compared to pristine epoxy plates.

Pretreatment methods for monitoring microplastics in soil and freshwater sediment samples: A comprehensive review.

This paper reviews the currently used pretreatment methods for microplastics (MPs) analysis in soil and freshwater sediments, primarily sample processing, pretreatment, and characterization methods for MPs analysis. In addition, analytical tools (e.g., lab instruments), MPs characteristics, and MPs quantity, are included in this review. Prior to pretreatment, soil and sediment samples are typically processed using sieving and drying methods, and a sample quantity of <50 g was mostly used for the pretreatment. Density separation was commonly performed before organic matter removal. Sodium chloride (NaCl) and zinc chloride (ZnCl2) were most often used for density separation, and hydrogen peroxide (H2O2) oxidation was most frequently used to remove organic matter. Although advantages of each pretreatment method have been investigated, it is still challenging to determine a universal pretreatment method due to sample variability (e.g., sample characteristics). Furthermore, it is highly required to establish standard pretreatment methods that can be used for various environmental matrices, including air, water, and wastes as well as soil and sediment.

Biodesalination using halophytic cyanobacterium Phormidium keutzingianum from brackish to the hypersaline water.

The biodesalination potential at different levels of salinity of Phormidium keutzingianum (P. keutzingianum) was investigated. A wide range of salinity from brackish to hypersaline water was explored in this study to ensure the adaptability of P. keutzingianum in extreme stress conditions. Brackish to hypersaline salt solutions were tested at selected NaCl concentrations 10, 30, 50, and 70 g.L-1. Chloride, pH, nitrate, and phosphate were the main parameters measured throughout the duration of the experiment. Biomass growth estimation revealed that the studied strain is adaptable to all the salinities inoculated. During the first growth phase (till day 20), chloride ion was removed up to 43.52% and 45.69% in 10 and 30 g.L-1 of salinity, respectively. Fourier transform infrared spectrometry analysis performed on P. keutzingianum showed the presence of active functional groups at all salinity levels, which resulted in biosorption leading to the bioaccumulation process. Samples for scanning electron microscopy (SEM) analysis supported with electron dispersive X-ray spectroscopy analysis (EDS) showed NaCl on samples already on day 0. This ensures the occurrence of the biosorption process. SEM-EDS results on 10th d showed evidence of additional ions deposited on the outer surface of P. keutzingianum. Calcium, magnesium, potassium, sodium, chloride, phosphorus, and iron were indicated in SEM-EDS analysis proving the occurrence of the biomineralization process. These findings confirmed that P. keutzingianum showed biomass production, biosorption, bioaccumulation, and biomineralization in all salinities; hence, the strain affirms the biodesalination process.

Nano-enabled pesticides for sustainable agriculture and global food security.

Achieving sustainable agricultural productivity and global food security are two of the biggest challenges of the new millennium. Addressing these challenges requires innovative technologies that can uplift global food production, while minimizing collateral environmental damage and preserving the resilience of agroecosystems against a rapidly changing climate. Nanomaterials with the ability to encapsulate and deliver pesticidal active ingredients (AIs) in a responsive (for example, controlled, targeted and synchronized) manner offer new opportunities to increase pesticidal efficacy and efficiency when compared with conventional pesticides. Here, we provide a comprehensive analysis of the key properties of nanopesticides in controlling agricultural pests for crop enhancement compared with their non-nanoscale analogues. Our analysis shows that when compared with non-nanoscale pesticides, the overall efficacy of nanopesticides against target organisms is 31.5% higher, including an 18.9% increased efficacy in field trials. Notably, the toxicity of nanopesticides toward non-target organisms is 43.1% lower, highlighting a decrease in collateral damage to the environment. The premature loss of AIs prior to reaching target organisms is reduced by 41.4%, paired with a 22.1% lower leaching potential of AIs in soils. Nanopesticides also render other benefits, including enhanced foliar adhesion, improved crop yield and quality, and a responsive nanoscale delivery platform of AIs to mitigate various pressing biotic and abiotic stresses (for example, heat, drought and salinity). Nonetheless, the uncertainties associated with the adverse effects of some nanopesticides are not well-understood, requiring further investigations. Overall, our findings show that nanopesticides are potentially more efficient, sustainable and resilient with lower adverse environmental impacts than their conventional analogues. These benefits, if harnessed appropriately, can promote higher crop yields and thus contribute towards sustainable agriculture and global food security.

Recent advances on PFAS degradation via thermal and nonthermal methods.

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.

Effect of colloid-size copper-based pesticides and wood-preservatives against microbial activities of Gram-positive Bacillus species using five-day biochemical oxygen demand test.

Copper-based pesticides and wood preservatives could end up in the environment during production, use, and end-of-life via different pathways that could cause unintended ecological and adverse health effects. This paper provides the effect of colloid-size Cu-based pesticides (CuPRO and Kocide), micronized Cu azole (MCA-1 and MCA-2) and alkaline Cu quaternary (ACQ) treated woods, Cu2+, Cu2+ spiked untreated wood (UTW), and CuCO3 solutions against Gram-positive Bacillus species using five-day biochemical oxygen demand (BOD5) standard test. The total Cu leached from MCA-1, MCA-2, and ACQ in Milli-Q water after 5 days were ~0.1, ~0.11, and ~0.64 g/kg of wood, respectively. However, the form of Cu leached from MCA woods was mostly ionic (> 90%). The total organic carbon (TOC) content of any tested wood (UTW/MCA-1/MCA-2/ACQ) was ~99% of its corresponding total carbon (TC) content, whereas the TOC of any tested wood sawdust exceeded that of its corresponding piece/block by > 300%. The dissolved oxygen (DO) consumption value in the presence of Cu2+, CuCO3, CuPRO, and Kocide solutions was significantly influenced by Cu particles/ions. However, the DO consumption value in the presence of UTW/MCA-1/MCA-2/ACQ woods was significantly influenced by organics leached from woods. On the other hand, the DO consumption of MCA sawdust was greater than (300%) that of MCA pieces/block. The findings of this study provide more insight into how organics leached from woods significantly reduce the toxic effects of Cu ions against Gram-positive Bacillus species.

Photooxidative decomposition and defluorination of perfluorooctanoic acid (PFOA) using an innovative technology of UV-vis/ZnxCu1-xFe2O4/oxalic acid.

Per- and polyfluoroalkyl substances (PFAS) are a large group of perfluorinated organic molecules that have been in use since the 1940s for industrial, commercial, and consumer applications. PFAS are a growing concern because some of them have shown persistent, bioaccumulative and toxic effects. Herein, we demonstrate an innovative technology of UV-vis/ZnxCu1-xFe2O4/oxalic acid for the degradation of perfluorooctanoic acid (PFOA) in water. The magnetically retrievable nanocrystalline heterogeneous ferrite catalysts, ZnxCu1-xFe2O4 were synthesized using a sol-gel auto-combustion process followed by calcination at 400 °C. The combination of ZnxCu1-xFe2O4 and oxalic acid generate reactive species under UV light irradiation. These reactive species are then shown to be capable of the photodegradation of PFOA. The degree of degradation is tracked by identifying transformation products using liquid chromatography coupled with quadrupole time-of-flight mass spectroscopy (LC-QTOF-MS).

Material recovery from electronic waste using pyrolysis: Emissions measurements and risk assessment.

Electronic waste (e-waste) generation has been growing in volume worldwide, and the diversity of its material composition is increasing. Sustainable management of this material is critical to achieving a circular-economy and minimizing environmental and public health risks. This study's objective was to investigate the use of pyrolysis as a possible technique to recover valuable materials and energy from different components of e-waste as an alternative approach for limiting their disposal to landfills. The study includes investigating the potential environmental impact of thermal processing of e-waste. The mass loss and change in e-waste chemicals during pyrolysis were also considered. The energy recovery from pyrolysis was made in a horizontal tube furnace under anoxic and isothermal conditions of selected temperatures of 300 °C, 400 °C, and 500 °C. Critical metals that include the rare earth elements and other metals (such as In, Co, Li) and valuable metals (Au, Ag, Pt group) were recovered from electronic components. Pyrolysis produced liquid and gas mixtures of organic compounds that can be used as fuels. Still, the process also emitted particulate matter and semi-volatile organic products, and the remaining ash contained leachable pollutants. Furthermore, toxicity characteristics leaching procedure (TCLP) of e-waste and partly oxidized products were conducted to measure the levels of pollutants leached before and after pyrolysis at selected temperatures. TCLP result revealed the presence of heavy metals like As, Cr, Cd, and Pd. Lead was found at 160 mg/L in PCBs leachate, which exceeded the toxicity characteristics (TC) limit of 5 mg/L. Liquid sample analysis from TCLP also showed the presence of C10-C19 components, including benzene. This study's results contribute to the development of practical recycling alternative approaches that could help reduce health risks and environmental problems and recover materials from e-waste. These results will also help assess the hazard risks that workers are exposed to semi-formal recycling centers.

A Sensitive Single Particle-ICP-MS Method for CeO2 Nanoparticles Analysis in Soil during Aging Process.

The increasing prevalence of products that incorporate engineered nanoparticles (ENPs) has prompted efforts to investigate the potential release, environmental fate, and exposure of the ENPs. However, the investigation of cerium dioxide nanoparticles (CeO2 NPs) in soil has remained limited, owing to the analytical challenge from the soil's complex nature. In this study, this challenge was overcome by applying a novel single particle-inductively coupled plasma-mass spectrometry (SP-ICP-MS) methodology to detect CeO2 NPs extracted from soil, utilizing tetrasodium pyrophosphate (TSPP) aqueous solution as an extractant. This method is highly sensitive for determining CeO2 NPs in soil, with detection limits of size and concentration of 15 nm and 194 NPs mL-1, respectively. Extraction efficiency was sufficient in the tested TSPP concentration range from 1 mM to 10 mM at a soil-to-extractant ratio 1:100 (g mL-1) for the extraction of CeO2 NPs from the soil spiked with CeO2 NPs. The aging study demonstrated that particle size, size distribution, and particle concentration underwent no significant change in the aged soils for a short period of one month. This study showed an efficient method capable of extracting and accurately determining CeO2 NPs in soil matrices. The method can serve as a useful tool for nanoparticle analysis in routine soil tests and soil research.

Indoor air pollution from cook-stoves during Injera baking in Ethiopia, exposure, and health risk assessment.

This study was undertaken to assess indoor air pollution and potential exposure to particulate matters (PMs-PM1, PM2.5, PM4, PM7, PM10), and total suspended particles [TSP] and total volatile organic compounds [TVOCs] during baking of Ethiopian traditional staple food, Injera using different types of stoves at Addis Ababa, Ethiopia. The geometric mean (GOM) of PMs pollutant using clean, improved, and traditional stoves were ranged 10.8-235, 23.6-462, and 36.4-591 µg/m3, respectively. The GOM of TVOCs in the wet and dry season using the clean, improved, and traditional stoves were 1,553, 2,234, 4,421, and 845, 1,214, and 2,662 µg/m3, respectively. The health risk of an exposed person to PM2.5, PM10, and TSP during baking of Injera was characterized and the results showed only baking of Injera using any of the stove types does not cause health problems to the baker. However, the percent contribution to the total chronic intake is high up to 38%.

Fates of Au, Ag, ZnO, and CeO2 Nanoparticles in Simulated Gastric Fluid Studied using Single-Particle-Inductively Coupled Plasma-Mass Spectrometry.

The increasing use of engineered nanoparticles (ENPs) in many industries has generated significant research interest regarding their impact on the environment and human health. The major routes of ENPs to enter the human body are inhalation, skin contact, and ingestion. Following ingestion, ENPs have a long contact time in the human stomach. Hence, it is essential to know the fate of the ENPs under gastric conditions. This study aims to investigate the fate of the widely used nanoparticles Ag-NP, Au-NP, CeO2-NP, and ZnO-NP in simulated gastric fluid (SGF) under different conditions through the application of single-particle inductively coupled plasma-mass spectrometry (SP-ICP-MS). The resulting analytical methods have size detection limits for Ag-NP, Au-NP, ZnO-NP, and CeO2-NP from 15 to 35 nm, and the particle concentration detection limit is 135 particles/mL. Metal ions corresponding to the ENPs of interest were detected simultaneously with detection limits from 0.02 to 0.1 µg/L. The results showed that ZnO-NPs dissolved completely and rapidly in SGF, whereas Au-NPs and CeO2-NPs showed apparent aggregation and did not dissolve significantly. Both aggregation and dissolution were observed in Ag-NP samples following exposure to SGF. The size distributions and concentrations of ENPs were affected by the original ENP concentration, ENP size, the contact time in SGF, and temperature. This work represents a significant advancement in the understanding of ENP characteristics under gastric conditions.

Role of water chemistry on stability, aggregation, and dissolution of uncoated and carbon-coated copper nanoparticles.

Intentional or accidental release of copper nanoparticles (Cu-NPs) from consumer products during manufacturing, use, and end-of-life management could pose health and ecological risks. This paper presents a detailed study on the role of water chemistry on the fate of uncoated and carbon-coated Cu-NPs dispersed in aqueous cetyltrimethylammonium bromide (CTAB) surfactant in the presence and absence of humic acids (HAs). A range of water chemistry and HAs had minimum impact on hydrodynamic diameter and zeta-potential values of uncoated and carbon-coated Cu-NPs. The water pH significantly (p < 0.001) affected the aggregation of uncoated Cu-NPs unlike that of carbon-coated Cu-NPs; however, the presence of HAs increased the stability of uncoated Cu-NPs. Although CTAB is considered as an efficient dispersant to stabilize Cu-NPs, the effect descended with time for uncoated Cu-NPs. The dissolution of Cu over time decreased with increasing pH for both uncoated (0.5-50% weight) and carbon-coated (0.5-40% weight) Cu-NPs. However, carbon-coated Cu-NPs exhibited significant dissolution (p < 0.001) at neutral pH than uncoated Cu-NPs may be due to the additional carbon it acquired during coating. Increasing HAs concentration from 0 to 15 mg L-1 at pH 5.5 inhibited aggregations but enhanced dissolution of the uncoated and carbon-coated Cu-NPs. These findings inform risk analysis of Cu-NPs including how Cu-NPs fate, mobility and bioavailability are modulated by particles coating and dispersant, HAs presence, water chemistry and exposure time in dispersion media.

Fragmentation of polymer nanocomposites: modulation by dry and wet weathering, fractionation, and nanomaterial filler.

In recent years, an increasing number of polymeric composites incorporating engineered nanomaterials (ENMs) have reached the market. Such nano-enabled products (NEPs) present enhanced performance through improved mechanical, thermal, UV protection, electrical, and gas barrier properties. However, little is known about how environmental weathering impacts ENM release, especially for high-tonnage NEPs like kaolin products, which have not been extensively examined by the scientific community. Here we study the simulated environmental weathering of different polymeric nanocomposites (epoxy, polyamide, polypropylene) filled with organic (multiwalled carbon nanotube, graphene, carbon black) and inorganic (WS2, SiO2, kaolin, Fe2O3, Cu-phthalocyanines) ENMs. Multiple techniques were employed by researchers at three laboratories to extensively evaluate the effect of weathering: ultraviolet-visible spectroscopy (UV-vis), Fourier transform infrared spectroscopy (FTIR), optical microscopy, contact angle measurements, gravimetric analysis, analytical ultracentrifugation (AUC), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and Raman spectroscopy. This work aimed to elucidate the extent to which weathering protocol (i.e. wet vs. dry) and diverse filler characteristics modulate fragment release and polymer matrix degradation. In doing so, it expanded the established NanoRelease protocol, previously used for analyzing fragment emission, by evaluating two significant additions: (1) simulated weathering with rain events and (2) fractionation of sample leachate prior to analysis. Comparing different composite materials and protocols demonstrated that the polymer matrix is the most significant factor in NEP aging. Wet weathering is more realistic than dry weathering, but dry weathering seems to provide a more controlled release of material over wet. Wet weathering studies could be complicated by leaching, and the addition of a fractionation step can improve the quality of UV-vis measurements.

Influence of water chemistry on colloid-size Cu-based pesticides particles: A case of Cu(OH)2 commercial fungicide/bactericide.

The intensive, widespread, and ever-increasing applications of Cu-based pesticides in agriculture could potentially increase environmental exposures via different routes. Unlike ionic/bulk forms, the fate, transport, and toxicity of colloid-size Cu-based pesticides are not well studied. This paper provides evaluation outcomes of granule and dispersion characterizations, stability, and dissolution of colloid-size particles of Cu(OH)2 commercial pesticide product at a range of water chemistry. The evaluated product contained about 35% weight of metallic Cu equivalent and Cu(OH)2 particles with sizes < 1 µm of which a fraction of nanoscale particles exist. The presence of Ca2+ at ionic strengths of >0.01 M and 0.001-0.2 M significantly influenced (p < 0.001) particle size (PS) and ζ-potential values, respectively at all investigated pH values. Cu dissolution at pH 5.5 was significant (p < 0.001) and exceeded Cu dissolutions at pH 7.0 by 87-90% and at pH 8.5 by 87-95% in all dispersions. The order of Cu dissolution was pH 5.5 > pH 7.0 > pH 8.5 in all dispersions. Cu dissolution was relatively reduced by 53% by increasing HA from 0 to 5 mg L-1 and enhanced by 55% by increasing HA from 5 to 15 mg L-1, however, the overall Cu dissolution was decreased by 27% by increasing HA from 0 to 15 mg L-1. Thus, HAs reduced the dissolution of Cu at pH < 7. The findings provide an insight into how water chemistry influences the fate and transport of colloid-size Cu-based pesticides particles.

Green and cytocompatible carboxyl modified gold-lysozyme nanoantibacterial for combating multidrug-resistant superbugs.

The dissemination of multi-drug resistant (MDR) superbugs in hospital environments, communities and food animals and the very dynamic bacterial mutation frequency require the development of prolonged therapeutic strategies to gain mastery over antibiotic resistance. A AuNP-lysozyme nanoantibacterial was fabricated by the conjugation of AuNPs-C6H4-4-COOH with lysozyme via green reduction of aryldiazonium gold(iii) salt [HOOC-4-C6H4N[triple bond, length as m-dash]N]AuCl4. Results from molecular docking calculations aimed at revealing the binding mode of benzoic acid with the lysozyme structure clearly showed the lowest energy conformation with benzoic acid bound in the deep buried hydrophobic cavity of the protein active site through strong hydrogen bonding and hydrophobic interactions, thus validating the experimental outcomes of the current study which also exhibited the binding of -COOH functional groups in the interior of the protein structure. The superiority of the lysozyme bioconjugate against superbugs was demonstrated by the enhanced and broadened lysozyme antibacterial activities of 98-99% against extended spectrum beta lactamase (ESBL) producing Escherichia coli and imipenem-resistant Pseudomonas aeruginosa clinical isolates and a selection of Gram-negative and Gram-positive standard ATCC strains. Selective toxicity against bacteria was confirmed by the high viability of HeLa and fibroblast cell lines and the outstanding hemocompatibility at the minimum bacterial inhibitory concentrations (MICs). Turbidimetric enzyme kinetic assay showed the enhancement of the lysozyme hydrolytic activity by gold nanoparticles on the Micrococcus lysodeikticus bacterial substrate. Using gel electrophoresis, the induced cell wall breakdown was confirmed by detecting the leaked-out bacterial genomic DNA. The integrity and morphology changes of the E. coli bacteria were investigated using a scanning electron microscope after one hour of contact with the lysozyme-gold bioconjugate. The antibacterial functionalities showed little or no damage to healthy human cells and can be applied to wound dressings and medical devices.

Characterization of colloid-size copper-based pesticide and its potential ecological implications.

The intensive use of Cu-based pesticides in agriculture could have an unintended impact on the ecosystems and human health via different exposure pathways. This paper presents the results of experiments involving colloidal stability, aggregation, and dissolution of Cu2O commercial pesticide under various environmental conditions in view of ecological implications. The investigated pesticide contains ∼750 g kg-1 Cu (75% weight of product), Cu2O particles with sizes < 1 µm, and nominal size fraction of Cu2O nanoparticles. The co-presence of Ca2+ (20 mM) and humic acid (HA, 15 mg L-1) significantly modulates (p < 0.001) the colloidal stability and mobility of particles. The dissolution of Cu at pH 5.5 was about 85%, 90%, and 75% weight more than the dissolution of Cu at pH 7.0, pH 8.5, and pH 7.0 and pH 8.5 combined, respectively in all dispersions. However, increasing HA content from 0 to 15 mg L-1 reduced the dissolution of Cu by 56%, 50%, and 40% weight at pH 5.5, 7.0, and 8.5, respectively. Thus, pH below 7.0 is a critical factor to control the dissolution and bioavailability of Cu that may pose ecotoxicity and environmental pollution, whereas pH above 7.0 and the presence of HA attenuate the pH effect. These findings provide insight into how the potential mobility and bioavailability of Cu is modulated by the water chemistry under various environmental scenarios and media.

Levels of trace elements in PM10 collected at roadsides of Addis Ababa, Ethiopia, and exposure risk assessment.

Estimation of personal exposure to air pollution is needed to identify high-risk population and to develop mitigation strategies. In this study, an assessment of the potential effects of short-term exposure to PM10 and the elements bound within PM10 was conducted. Samples were obtained from the ten sub-cities of Addis Ababa (three sampling points from each) during the commuting time (traffic congestion and taxi queues). A particle counter consisting of a portable sampling unit with multi-fraction dust samplers was used for sample collection. The elemental composition was analyzed by inductively coupled plasma-optical emission spectroscopy (ICP-OES). The mean concentrations of PM10 ranged from 206 to 308 µg m-3. The highest concentrations of pollutants were found in the major open-market part of the city, Addis Ketema. The lowest concentrations were found at the old-town, Arada sub-cities. The concentration of trace elements (Fe, Cd, As, Cr, Pb, B, Ni, Co, Sn, Cu, and Zn) bound in PM10 ranged from below detectable limit to 0.981 µg m-3. Regardless of the sampling sub-city, the overall patterns of the mean concentration of elements bound in PM10 were found in the following increasing order of Cr < Cd < As < Co < Ni < Cu < Fe < Pb < Sn < B < Zn < Mn. The results showed that the primary source of Zn, Cr, and Cd may be emissions from on-road vehicles, tire and brake wear. Pb originates mainly from industries and suspended soil dust at the roadside, whereas As, Mn, and B are associated with dust resuspension and biomass and biofuel combustion, respectively. The carcinogenic and non-carcinogenic risks due to chronic exposure to trace elements bound in PM10 at the roadside were assessed in accordance with the U.S. Environmental Protection Agency (US EPA) guidelines. It was determined that Mn, As, and Cd contributed substantially to the inducement of non-carcinogenic health problems to children and adults as a result of exposure while in close proximity to the roadsides.

Bio-desalination of brackish and seawater using halophytic algae.

Global demand for water is rising. A sustainable and energy efficient approach is needed to desalinate brackish sources for agricultural and municipal water use. Genetic variation among two algae species, Scenedesmus species (S. sp.) and Chlorella vulgaris (C. vulgaris), in their tolerance and uptake of salt (NaCl) was examined for potential bio-desalination of brackish water. Salt-tolerant hyper-accumulators were evaluated in a batch photobioreactors over salinity concentration ranging from 2 g/L to 20 g/L and different nutrient composition for their growth rate and salt-uptake. During algae growth phase, the doubling time varied between 0.63 and 1.81 days for S. sp. and 3.1 to 5.9 for C. vulgaris. The initial salt-uptake followed pseudo first order kinetics where the rate constant ranged between -3.58 and -7.68 day-1 reaching up to 30% in a single cycle. The halophyte algae S. sp. and C. vulgaris that were selected for pilot-scale studies here represent a promising new method for desalination of brackish waters. Halophytic technologies combined with the potential use of algae for biofuel, which offsets energy demand, can provide a sustainable solution for clean, affordable water and energy.