Water Concentration Research Articles

Experimental and DFT calculation study on the efficient removal of high fluoride wastewater from metallurgical wastewater by kaolinite

Fluoride pollution and water scarcity are urgent issues. Reducing fluoride concentration in water is crucial. Kaolinite has been used to study adsorption and fluoride removal in water and to characterize material properties. The experimental results showed that the adsorption capacity of kaolinite decreased with increasing pH. The highest adsorption of fluoride occurred at pH 2, with a capacity of 11.1 mg/g. The fluoride removal efficiency remained high after four regeneration cycles. The fitting results with the Freundlich isotherm model and the external diffusion model showed that the non-homogeneous adsorption of kaolinite fit the adsorption behavior better. Finally, the adsorption mechanism was analyzed by FT-IR and XPS. The binding energies of various adsorption sites and the chemical adsorption properties of atomic states were discussed in relation to DFT calculations. The results showed that Al and H sites were the main binding sites, and the bonding stability for different forms of fluoride varies, with the size of Al–F (−7.498 eV) > H–F (−6.04 eV) > H–HF (−3.439 eV) > Al–HF (−3.283 eV). Furthermore, the density of states and Mulliken charge distribution revealed that the 2p orbital of F was found to be active in the adsorption process and was the main orbital for charge transfer.

A biosensor monitoring approach for toxic algae: Construction of calibration curves to infer cell numbers in field material

A variety of shellfish toxin-producing Harmful Algal Blooms (HABs) occur every year in coastal temperate waters worldwide. These toxic HABs may cause lengthy (months) harvesting bans of mussels and other suspension feeding bivalves exposed to their blooms. To safeguard public health and the shellfish industry, European Union regulations request periodic monitoring of potentially toxic microalgae in seawater and phycotoxins in live bivalve molluscs from shellfish production areas. Monitoring of other toxic microalgae, e.g., fish killers, is based solely on cell counts. Morphological identification and quantification of microalgal cells with light microscopy is time-consuming, requires a good expertise, and accurate identification to species level (e.g., Pseudo-nitzschia species) may require electron microscopy. Toxicity varies among morphologically similar species; there are toxic and non-toxic strains of the same species. Molecular techniques using ribosomal DNA sequences offer a possibility to identify and detect precisely the potentially toxic genus/species. In an earlier project (MIDTAL), specific probes against rRNA sequences of all HAB taxa, known at the time of the project, affecting shellfish areas worldwide were designed, and those affecting Europe were tested and calibrated against rRNA extracts of clonal cultures and field samples. Microarray technology was adopted to relate to cell numbers the fluorescence signal from the reaction of all target species probes spotted in the microarray slides with those present in a single sample extract. The EMERTOX project aimed to develop a more automatic “Lab on a chip” (LOC) technology, including a non- (cell) disruptive water concentration system and biosensors for HAB cells detection. Here, calibration curves are presented against toxic microalgae (cultures and field samples) causing endemic and emerging toxicity events in Galicia (NW Spain) and Portugal. Results here relating cell numbers to electrochemical signals will be used in an early warning biosensor for toxic algae.

Occurrence and potential ecological risks of PFAS in Pampulha Lake, Brazil, a UNESCO world heritage site

Per- and polyfluoroalkyl substances (PFAS) comprise >4000 synthetic substances used in industrial applications and consumer products. PFAS used daily in households and manufacturing plants end up in domestic sewage, and industrial effluents can be discharged to surface water. Urban watersheds located in low and middle-income countries (LMIC), which lack sanitation infrastructure, are potential recipients of waste containing PFAS. Yet, only a few studies report PFAS occurrence in urban reservoirs and lakes, especially those located in the Global South due to resource limitations. This is the first study aimed to assess PFAS occurrence and ecological risks in Pampulha Lake, Brazil, a site which represents the reality of many other urban watersheds in LMIC as it is surrounded by densely populated areas and manufacturing plants. Surface water samples were collected monthly for 1 year from four sampling points at Pampulha Lake. Sample analysis was based on US Environmental Protection Agency Method 1633, which employs solid phase extraction followed by liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS). Species sensitivity distribution (SSD) curves were built to identify potentially susceptible species based on detected water concentrations. Bioaccumulation was estimated for fish tissue. Short-chain (perfluorobutanesulfonic acid, PFBS and perfluorohexanoic acid, PFHxA) and long-chain PFAS (perfluorodecanoic acid, PFDA; perfluorooctanoic acid, PFOA; perfluorododecanoic acid, PFDoA; and perfluorooctanesulfonic acid, PFOS) were detected at the μg L−1 range. Total PFAS concentrations in the wet season were generally higher than in the dry season, likely due to limited capacity of the treatment plant processing water from tributaries which receive raw sewage. More than 5 % of aquatic species are potentially susceptible to chronic effects of PFOS at detected concentrations (0.2–2.2 μg L−1). Predicted bioaccumulation of PFOS in fish was above advisory diet intake levels for humans. Results emphasize the need for studies related to PFAS occurrence in watersheds located in LMIC.

Response of dissolved inorganic carbon dynamics to simulated tidal hydrological processes in coastal wetlands

To clarify the impacts of tidal hydrological process shifts caused by sea level rise on the blue carbon cycle, a typical coastal wetland in Jiaozhou Bay was selected for this study. The soils of Suaeda salsa (SS) and Phragmites australis (PA) wetlands were collected to simulate the effects of three types of tidal hydrological processes (Neap tide group, NT; Middle tide group, MT; Spring tide group, ST) on the soil-water dissolved inorganic carbon (DIC) dynamic. The results showed that the concentration of water dissolved inorganic carbon (WDIC) increased rapidly (115% higher) at early stage (days 0–4) under the influence of the tidal hydrological processes. Significant differences were found in WDIC concentration during different tidal hydrological processes (P < 0.05), which were expressed as MT (52.7 ± 13.3 mg L−1) > ST (52.5 ± 12.9 mg L−1) > NT (48.4 ± 10.1 mg L−1). After experiencing the tidal hydrological processes, the soil DIC content showed a net accumulation (55.1 ± 1.29 mg L−1vs. 46.7 ± 1.76 mg L−1, P < 0.001), whereas the soil inorganic carbon (SIC) decreased (2.73 ± 1.64 mg L−1vs. 4.61 ± 1.71 mg L−1), which may be attributed to the dissolution of SIC caused by the uptake of CO2 to form DIC. The accumulation of soil DIC was directly related to the SIC (λ = 1.03, P < 0.01), and indirectly related to soil nutrients (SOC substrate, λ = −0.003) and microbes (microbial biomass, λ = −0.10), and was mainly dominated by abiotic processes (abiotic: 58.1 ± 1.8% to 82.7 ± 2.46% vs. biotic: 17.4 ± 2.46% to 41.9 ± 1.76%). The increase of tidal frequency generally inhibited the accumulation of soil DIC content and promoted the output of WDIC. However, the response of soil DIC in different wetland types to tidal frequency was divergent, which was mainly regulated by the trade-off between soil nutrients and SIC content. Taken together, tidal hydrological processes and their frequency changes reshaped DIC dynamics, promoted the dissolution of SIC and the potential uptake of CO2. These findings enhance the comprehension of the inorganic carbon cycle within coastal wetlands, particularly amidst the backdrop of climate change and the rising sea levels.

Introducing Hydrogen-Bonding Microenvironment in Close Proximity to Single-Atom Sites for Boosting Photocatalytic Hydrogen Production.

Inspired by enzymatic catalysis, it is crucial to construct hydrogen-bonding-rich microenvironment around catalytic sites; unfortunately, its precise construction and understanding how the distance between such microenvironment and catalytic sites affects the catalysis remain significantly challenging. In this work, a series of metal-organic framework (MOF)-based single-atom Ru1 catalysts, namely, Ru1/UiO-67-X (X = -H, -m-(NH2)2, -o-(NH2)2), have been synthesized, where the distance between the hydrogen-bonding microenvironment and Ru1 sites is modulated by altering the location of amino groups. The -NH2 group can form hydrogen bonds with H2O, constituting a unique microenvironment that causes an increased water concentration around the Ru1 sites. Remarkably, Ru1/UiO-67-o-(NH2)2 displays a superior photocatalytic hydrogen production rate, ∼4.6 and ∼146.6 times of Ru1/UiO-67-m-(NH2)2 and Ru1/UiO-67, respectively. Both experimental and computational results suggest that the close proximity of amino groups to the Ru1 sites in Ru1/UiO-67-o-(NH2)2 improves charge transfer and H2O dissociation, accounting for the promoted photocatalytic hydrogen production.

Operando FTIR study on water additive in lithium-sulfur batteries to mitigate shuttle effect

Additives in the electrolytes of Li-S batteries aim to increase overall capacity, improve Li+ ion conductivity, enhance cyclability, and mitigate the shuttle effect, which is one of the major issues of this system. Here, the use of water as an additive in the commonly used electrolyte, 1.0 M LiTFSI/1.0% (w/w) LiNO3 and a 1:1 mixture of 1,3-dioxolane (DOL) and 1,2-dimethoxyethane (DME) was investigated. We used Co2Mn0.5Al0.5O4 (CMA) as an electrocatalyst anchored on an activated carbon (AC) electrode with added sulfur via a melt-diffusion process. The structural analysis of CMA via Rietveld refinement showed interatomic spaces that can promote ionic conductivity, facilitating Li+ ion migration. Electrochemical tests determined 1600 ppm as the optimal water concentration, significantly reducing the shuttle effect. Post-mortem XPS analysis focused on the lithium metal anode revealed the formation of Li2O layers in dry samples and LiOH in wet samples. Better capacity was observed in wet samples, which can be attributed to the superior ionic conductivity of LiOH at the electrode/electrolyte interface, surpassing that of Li2O by 12 times. Finally, Operando FTIR experiments provided real-time insights into electrolyte degradation and SEI formation, elucidating the activity mechanisms of water and Li2CO3 over the cycles. This work presents results that could aid future advancements in Li-S battery technology, offering possibilities to mitigate its challenges with inexpensive and scalable additives.

Rapid Colorimetric Detection of Ca(II) Based on Surface Plasmon Resonance Absorbances of 5‐PBA@AuNPs Sensor

Calcium ions (Ca2+) are essential for a myriad of physiological functions, including excitability, neurotransmitter release, gene transcription, cell proliferation, synaptic plasticity, and hormone secretion. Consequently, the detection of Ca2+ concentrations in water is of fundamental and practical significance. In this study, a novel method for the simple, visual, and rapid colorimetric detection of Ca2+ is introduced, leveraging the surface plasmon resonance (SPR) absorbances of gold nanoparticles (AuNPs) modified with 5‐Pyrimidinylboronic acid (5‐PBA). A color change from wine‐red to gray‐blue was observed with increasing concentrations of Ca2+, indicative of the agglomeration of AuNPs. This agglomeration displayed favorable anti‐interference properties and selectivity. The limits of detection (LOD) were determined to be 0.08 mM by the unaided eye and 3.29 μM by UV‐visible spectroscopy. Moreover, an excellent linear relationship (R2 = 0.9879) was maintained within the Ca2+ concentration range of 0.0 to 0.5 mM. These results suggest that AuNPs modified with 5‐PBA are suitable for the quantitative determination of Ca2+. Subsequent testing on actual samples confirmed that this new method could be effectively applied to the monitoring of Ca2+ in water.

Spatial heterogeneity, sediment-water exchange, and diffusion mechanisms of organophosphate esters from river to coastal aquatic system in a typical economic circle of northern China

Organophosphate esters (OPEs) have proven to be pervasive in aquatic environments globally. However, understanding their partitioning behavior and mechanisms at the sediment-water interface remains limited. This study elucidated the spatial heterogeneity, interfacial exchange, and diffusion mechanisms of 14 OPEs (∑14OPEs) from river to coastal aquatic system. The transport tendencies of OPEs at the sediment-water interface were quantitatively assessed using fugacity methods. The total ∑14OPEs concentrations in water and sediments ranged from 154 ng/L to 528 ng/L and 2.41 ng/g dry weight (dw) to 230 ng/g dw, respectively. This result indicated a descending spatial tendency with moderate variability. OPE distribution was primarily influenced by temperature, pH, and dissolved oxygen levels. As the carbon atom number increased, alkyl and chlorinated OPEs transitioned from diffusion towards the aqueous phase to equilibrium. In contrast, aryl OPEs and triphenylphosphine oxide, which had equivalent carbon atom counts, maintained equilibrium throughout. Diffusion trends of individual OPE congener at the sediment-water interface varied at the same total organic carbon contents (foc). As the foc increased, the fugacity fraction values for all OPE homologs showed a declining trend. The distinct molecular structure of each OPE monomer might lead to unique diffusive behaviors at the sediment-water interface. Higher soot carbon content had a more pronounced effect on the distribution patterns of OPEs. The sediment-water distribution of OPEs was primarily influenced by total organic carbon, sediment particle size, dry density, and moisture content. OPEs displayed the highest sensitivity to fluctuations in ammonium and dissolved organic carbon. This study holds significant scientific and theoretical implications for elucidating the interfacial transport and driving forces of OPEs and comprehending their fate and endogenous release in aquatic ecosystems.

Inhibit ammonia volatilization from agriculture and livestock by air plasma-activated water

Ammonia volatilization in agriculture and livestock is a considerable cause of air pollution and a significant way of N loss. In this study, we propose a method of using air plasma-activated water (PAW) to inhibit ammonia volatilization from agriculture and livestock and report the inhibitory effect under different discharge times and concentration gradients. PAW was generated through needle–water discharge, while ammonia waters with different concentrations served as simplified models for ammonia release. The compositions of the gas/liquid products of the PAW and those after mixing with ammonia water were detected and analyzed. It was found that the PAW could effectively inhibit the NH3 volatilization from ammonia water over a large range of conditions, however, NH3 volatilization promotion could also happen in some cases. The inhibition rate (IR) generally increased with the longer discharge time of the PAW and decreased with the higher ammonia water concentration. As the discharge time increased, the PAW became more acidic and had more active N components, converting more volatile NH3 to NH4 + when mixed with ammonia water. Finally, a relationship model was developed between the IR and pH of the mixture. The IR basically decreased with the increase of the mixture pH, and reached ∼100% when a PAW with a discharge time of 7.5 min or 10 min was mixed with ammonia water with a mass fraction of 0.15%, or PAW of 10 min mixed with 0.25% ammonia water in this study, with the mixture pH lower than 8. The basic chemical process and possible reaction mechanisms were discussed. The proposed method not only effectively reduces ammonia volatilization but also adds more N elements in the form of NO3 − and NH4 +, which further improves fertility.

Analysis of Spatiotemporal Variation and Driving Factors of Water Quality in the Xiangjiang River Basin from 1990 to 2016

In order to explore the spatiotemporal variation characteristics and driving mechanism of water quality in the Xiangjiang River Basin, the data of 16 water quality parameters at 113 stations over 26 years from 1990 to 2016 in the Xiangjiang River Basin were collected for synthetically assessing the water quality and identifying its main pollutants through the water quality index and other methods. The causal mechanism of water quality, especially the driving effect of water level and land use pattern, was analyzed. The results showed that： ① The overall water quality grade of the Xiangjiang River Basin during the study period was "good." However, the water quality deteriorated first （from 1990 to 2003） and then improved （from 2004 to 2016）. The season variation in water quality was not obvious, but the water quality fluctuation of the wet season was larger. The water pollution load of the main stream decreased successively from the middle reaches, downstream reaches, and upstream reaches. The upstream tributaries had the best water quality, whereas areas with poor water quality were mainly distributed at the mouth of the middle and downstream tributaries, especially in areas where multiple tributaries converged. ② Toxic heavy metals had the characteristics of toxicity, persistence, and bioaccumulation. If they exceeded a certain concentration in water, they were difficult to purify, posing great harm to the natural environment and human health. The toxic metal index （CI1） was the leading factor affecting water quality, in which Hg and Cd were the main parameters affecting the overall water quality of the Xiangjiang River Basin. ③ The water level had a positive impact on the water quality of the Xiangjiang River by diluting environmental parameters. Land type had little effect on heavy metal concentration, whereas forest land could improve water quality. Grassland had a negative correlation with permanganate index over a large scale range （≥ 5 km）. The increase in water bodies, arable land, and impermeable surface areas within the watershed increased the probability of high fecal coliform concentration in the water body. ④ With the increase in buffer distance, the water quality explained by the land use pattern increased. On the scale of 10 km buffer zone in the riparian zone, the explanation degree by land use pattern on water quality was the highest, which was an effective scale for water quality control of the Xiangjiang River. This research showed that the driving factors of heavy metal pollution and other pollution were different, but their regional differences were all obvious in the Xiangjiang River Basin. Therefore, pollution control should be classified and taken according to local conditions.

Unraveling relationship between complex lifetimes and microscopic diffusion in deep eutectic solvents.

Aqueous mixtures of deep eutectic solvents (DESs) have emerged as a subject of interest in recent years for their tailored physicochemical properties. However, a comprehensive understanding of water's multifaceted influence on the microscopic dynamics, including its impact on improved transport properties of the DES, remains elusive. Additionally, the diffusion mechanisms within DESs manifest heterogeneous behavior, intricately tied to the formation and dissociation kinetics of complexes and hydrogen bonds. Therefore, it is imperative to explore the intricate interplay between bond kinetics, diffusion mechanism, and dynamical heterogeneity. This work employs water as an agent to explore their relationships by studying various relaxation phenomena in a DES based on acetamide and lithium perchlorate over a wide range of water concentrations. Notably, acetamide exhibits Fickian yet non-Gaussian diffusion across all water concentrations with Fickian (τf) and Gaussian (τg) timescales following a power-law relationship, τg∝τfγ, γ ∼ 1.4. The strength of coupling between bond kinetics and different diffusion timescales is estimated through various power-law relationships. Notably, acetamide-water hydrogen bond lifetime is linked to diffusive timescales through a single power-law over the entire water concentration studied. However, the relationship between diffusive timescales and the lifetime of acetamide-lithium complexes shows a sharp transition in behavior at 20 wt. % water, reflecting a change from vehicular diffusion below this concentration to structural diffusion above it. Our findings emphasize the critical importance of understanding bond dynamics within DESs, as they closely correlate with and regulate the molecular diffusion processes within these systems.

Assessment of Microplastic Content in Surface Waters of the Russian Part of the Sea of Japan Basin

Assessment of Microplastic Content in Surface Waters of the Russian Part of the Sea of Japan Basin

Exploring freshwater stream bacterial communities as indicators of land use intensity

BackgroundStream ecosystems comprise complex interactions among biological communities and their physicochemical surroundings, contributing to their overall ecological health. Despite this, many monitoring programs ignore changes in the bacterial communities that are the base of food webs in streams, often focusing on stream physicochemical assessments or macroinvertebrate community diversity instead. We used 16S rRNA gene sequencing to assess bacterial community compositions within 600 New Zealand stream biofilm samples from 204 sites within a 6-week period (February–March 2010). Sites were either dominated by indigenous forests, exotic plantation forests, horticulture, or pastoral grasslands in the upstream catchment. We sought to predict each site’s catchment land use and environmental conditions based on the composition of the stream bacterial communities.ResultsRandom forest modelling allowed us to use bacterial community composition to predict upstream catchment land use with 65% accuracy; urban sites were correctly assigned 90% of the time. Despite the variation inherent when sampling across a ~ 1000-km distance, bacterial community data could correctly differentiate undisturbed sites, grouped by their dominant environmental properties, with 75% accuracy. The positive correlations between actual values and those predicted by the models built using the stream biofilm bacterial data ranged from weak (average log N concentration in the stream water, R2 = 0.02) to strong (annual mean air temperature, R2 = 0.69).ConclusionsFreshwater bacterial community data provide useful insights into land use impacts on stream ecosystems; they may be used as an additional measure to screen stream catchment attributes.

Arsenic distribution characteristics and release mechanisms in aquaculture lake sediments

It is well known that aquaculture can alter the microenvironments of lakes at sediment-water interface (SWI). However, the main mechanisms underlying the effects of aquaculture activities on arsenic (As) transformations are still unclear. In this context, the present study aims to investigate the variations in the sediment As contents in Yangcheng Lake, as well as to assess its chemical transformations, release fluxes, and release mechanisms. The results showed substantial spatial differences in the dissolved As concentrations in the sediment pore water. The As release fluxes at the SWI ranged from 1.32 to 112.09 μg/L, with an average value of 33.68 μg/L. In addition, the highest As fluxes were observed in the aquaculture areas. The transformation of crystalline hydrous Fe oxide-bound As to adsorbed-As in the aquaculture lake sediments increased the ability of As release. The Partial least squares path modeling results demonstrated the great contributions of organic matter (OM) to the As transformations by influencing the sediment microbial communities and Fe/Mn minerals. The changes in the As fractionation and competing adsorption increased the dissolved As concentrations in the 0–10 mm surface sediment. Non-specifically and specifically adsorbed As were the major sources of dissolved As in the sediments. Specifically, microbial reduction of As[V] and dissolution of Fe oxides increased the dissolved As concentrations at the SWI (20 to −20 mm). The results of the current study highlight the positive enhancement effects of aquaculture on As release from sediments.

Investigation on ion concentration of pore water in compacted bentonite after infiltrated by salt solutions

The behavior of salt solutions infiltrated into compacted bentonite was investigated in this study, with particular attention paid to the ion concentration in the pore water, in order to improve the understanding of the bentonite behavior in geological disposal projects. A Japanese bentonite, Kunigel V1 (K_V1), was used to prepare specimens with a thickness of 2 mm and an initial dry density of 1.4 to 1.7 Mg/m3. For each density case, salt solutions (NaCl, KCl, and CaCl2) of different amounts (0 to 2 mol/L) were supplied to the specimens. After infiltration, the basal spacing (d001) and exchangeable cations of the montmorillonite in the bentonite and the leached cations from the bentonite were measured. Based on the test results, the ion concentration in the interlayer pore water of the montmorillonite or the interparticle pore water was discussed. The findings indicated that the infiltration capacities of the various salt solutions into the compacted K_V1 bentonite were in the order of KCl > CaCl2 > NaCl. The K_V1 specimen with the highest initial dry density exhibited the strongest resistance to salt solution infiltration. After the infiltration of the NaCl solution into the compacted K_V1 bentonite, the increased sodium ions mainly remained in the interparticle pores, leading to an increase in the sodium ion concentration in the interparticle pore water. During the infiltration of the KCl and CaCl2 solutions into the compacted K_V1 bentonite, the infiltrated potassium ions in the case of KC1 and the calcium ions in the case of CaCl2 tended to penetrate the interlayer pore preferentially, thereby displacing the exchangeable sodium ions. After most of the exchangeable sodium ions that had initially existed in the montmorillonite had been replaced, the infiltrated potassium or calcium ions remained in the interparticle pores.

Impact of total phenolic compounds on ecological and health risks of water and sediments from Timsah Lake, Suez Canal, Egypt.

This study aimed to measure spatial and temporal distributions of total phenolic compounds and their ecological and health hazards using UV-vis spectrophotometers as a low-cost, fast, simple method in water and sediments collected from Timsah Lake, Suez Canal, Egypt, 2022. Also, assessing highly adaptive fungal species associated with contamination is designed. Due to human and environmental activities and industrial waste discharges, Timsah Lake is increasingly threatened by all kinds of pollutants. The results indicated that the seasonal concentration means of the phenolic compounds were winter (0.229) > spring (0.161) > summer (0.124) > autumn (0.131) mg/l and winter (3.08) > summer (2.66) mg/g in water and sediment samples, respectively. The result has shown that the phenol concentrations in all stations were more than 0.005 and 0.1 mg/l for Egyptian National Standards and World Health Organization (WHO) for drinking water but less than the limits of 1 mg/l for wastewater. Notably, the fungi recorded the highest counts during spring, totaling 397 colonies/100 ml of water and 842 colonies/gram of sediment. Four isolates of fungi were identified and deposited in the GenBank database by Aspergillus terreus, Aspergillus terreus, Penicillium roqueforti, and Penicillium rubens under accession numbers OR401933, OR402837, OR402878, and OR424729, respectively. Moreover, ecological risk (RQ) for the total phenolic compounds was > 1 in all investigated stations for water and sediments. The hazard quotient is HQ < 1 in all seasons in water and sediments except winter. The hazard index (HI) in water and sediments for children is higher than for adults. It can be concluded that the low-cost, fast, simple method for determining phenolic content in water and sediment samples, using UV-vis spectrophotometry, was useful for predicting the reactivates of a wide variety of phenol and their derivatives. Furthermore, it can be concluded that Periodic assessments of water quality and strict regulations are necessary to safeguard this vital resource from pollution and ensure the well-being of future generations. Finally, policymakers and water treatment specialists might use the information from this research to reduce these chemical pollutants in Egypt.

Waste PET bottles derived carbon black as electrode material for supercapacitor application

This study explores the conversion of polyethylene terephthalate (PET) waste into carbon black for its use in supercapacitors, offering a sustainable solution to waste management and energy storage needs. PET bottles were pyrolysed in an inert environment to produce carbon black. This plastic waste derived carbon was then characterised and used for electrode fabrication to explore its potential in supercapacitor applications. The supercapacitive properties of these electrodes were evaluated using cyclic voltammetry and charge–discharge techniques in various “Water-in-salt” electrolytes (WIS). WIS are the electrolytes in which the concentration of water is less than the concentration of salts by weight and volume. electrolytes. Sodium acetate (CH3COONa) exhibited the highest potential window and specific capacitance among the tested electrolytes. The derived carbon black demonstrated promising electrochemical performance, with a specific capacitance of 233 F/g and an energy density of 186.6 Wh/kg. These findings underscore the potential of carbon black derived from waste PET bottles as an effective material for supercapacitors, contributing to sustainable energy storage solutions and waste reduction.

Dietary Iodine Intake and Sources among Residents in Zhejiang Province 10 Years after Reducing Iodine Concentration in Iodized Salt.

We aimed to assess dietary iodine intake and sources in Zhejiang Province a decade after a reduction in iodine concentration in iodized salt. Three-day 24 h dietary recall and household weighing were used, complemented by "Chinese Food Composition" data. Household water and salt samples were collected from 5890 residents and analyzed. Differences in iodized salt consumption rates were observed across the following regions: inland (84.20%), subcoastal (67.80%), and coastal (37.00%) areas. The median (P25, P75) iodine concentration in water and diet were 2.2 (0.9, 4.0) μg/L and 142.05 (58.94, 237.11) μg/d, respectively, with significant regional differences in dietary concentration (inland [185.61 μg/d], subcoastal [153.42 μg/d], and coastal [75.66 μg/d]). Males (149.99 μg/d) and iodized salt consumers (191.98 μg/d) had a significantly higher dietary iodine intake than their counterparts. Regions were ranked as follows based on the proportions of individuals meeting the recommended dietary iodine intake: inland (69.40%), subcoastal (56.50%), and coastal (34.10%) areas. Dietary sources included salt (48.54%), other foods (32.06%), drinking water (8.84%), laver (4.82%), kelp (3.02%), and other seafood (2.32%). The qualified iodized salt consumption rate was significantly lower than the national standard. Zhejiang Province should continue implementing measures to control iodine deficiency through salt iodization, education efforts, and increasing the qualified iodized salt consumption rate.

New Insights into the Formation of Aggregates of Bidisperse Nano- and Microplastics in Water Based on the Analysis of In Situ Microscopy and Molecular Simulation.

Microplastics (MPs) and nanoplastics (NPs) in water pose a global threat to human health and the environment. To develop efficient removal strategies, it is crucial to understand how these particles behave as they aggregate. However, our knowledge of the process of aggregate formation from primary particles of different sizes is limited. In this study, we analyzed the growth kinetics and structures of aggregates formed by polystyrene MPs in mono- and bidisperse systems using in situ microscopy and image analysis. Our findings show that the scaling behavior of aggregate growth remains unaffected by the primary particle size distribution, but it does delay the onset of rapid aggregation. We also performed a structural analysis that reveals the power law dependence of aggregate fractal dimension (df) in both mono- and bidisperse systems, with mean df consistent with diffusion-limited cluster aggregation (DLCA) aggregates. Our results also suggest that the df of aggregates is insensitive to the shape anisotropy. We simulated molecular forces driving aggregation of polystyrene NPs of different sizes under high ionic strength conditions. These conditions represent salt concentration in ocean water and wastewater, where the DLVO theory does not apply. Our simulation results show that the aggregation tendency of the NPs increases with the ionic strength. The increase in the aggregation is caused by the depletion of clusters of ions from the NPs surface.

Palladium-Catalyzed Amination of Aryl Halides with Aqueous Ammonia and Hydroxide Base Enabled by Ligand Development.

The conversion of aryl halides to primary arylamines with a convenient and inexpensive source of ammonia has been a long-standing synthetic challenge. Aqueous ammonia would be the most convenient and least expensive form of ammonia, but such a palladium-catalyzed amination reaction with a high concentration of water faces challenges concerning catalyst stability and competing hydroxylation, and palladium-catalyzed reactions with this practical reagent are rare. Further, most reactions with ammonia to form primary amines are conducted with tert-butoxide base, but reactions with ammonium hydroxide would contain hydroxide as base. Thus, ammonia surrogates, ammonia in organic solvents, and ammonium salts have been used under anhydrous conditions instead with varying levels of selectivity for the primary amine. We report the palladium-catalyzed amination of aryl and heteroaryl chlorides and bromides with aqueous ammonia and a hydroxide base to form the primary arylamine with high selectivity. The palladium catalyst containing a new dialkyl biheteroaryl phosphine ligand (KPhos) suppresses both the formation of aryl alcohol and diarylamine side products. Mechanistic studies with a soluble hydroxide base revealed turnover-limiting reductive elimination of the arylamine and an equilibrium between arylpalladium amido and hydroxo complexes prior to the turnover-limiting step.