High Cation Concentrations Research Articles

Soil acidification controls invasive plant species in the restoration of degraded Cerrado grasslands

The Cerrado, South America's largest savanna, has acidic, nutrient‐poor soils and its native plants thrive under these conditions. However, abandoned pastures historically undergo changes in chemical properties due to interventions like liming and fertilizer use. This favors invasive African grasses and hinders native plants, impacting restoration efforts. In a Cerrado grassland undergoing restoration study, we tested whether soil acidification could restore native soil conditions and control invasives using 56 plots across 14 blocks. We hypothesized that decreased soil pH and nutrient availability would reduce invasive biomass and enhance diversity. We show that acidification reduced invasive biomass by 71%, with acidification negatively affecting invasives while sparing natives. Maintaining nutrient‐poor soil conditions can help to control invasive grasses in restoration projects, as fertilizer application can favor invasive species establishment. Soil acidification effectiveness depends on local nutrient levels. Areas with high soil cation content may require larger amendment quantities. Restoration strategies in nutrient‐poor ecosystems should aim recovering historical soil conditions to control invasives growth and support slow‐growing native plants.

Preventing acute neurotoxicity of CNS therapeutic oligonucleotides with the addition of Ca2+ and Mg2+ in the formulation

Oligonucleotide therapeutics (ASOs and siRNAs) have been explored for modulation of gene expression in the central nervous system (CNS), with several drugs approved and many in clinical evaluation. Administration of highly concentrated oligonucleotides to the CNS can induce acute neurotoxicity. We demonstrate that delivery of concentrated oligonucleotides to the CSF in awake mice induces acute toxicity, observable within seconds of injection. Electroencephalography (EEG) and electromyography (EMG) in awake mice demonstrated seizures. Using ion chromatography, we show that siRNAs can tightly bind Ca2+ and Mg2+ up to molar equivalents of the phosphodiester (PO)/phosphorothioate (PS) bonds independently of the structure or phosphorothioate content. Optimization of the formulation by adding high concentrations (above biological levels) of divalent cations (Ca2+ alone, Mg2+ alone, or Ca2+ and Mg2+) prevents seizures with no impact on the distribution or efficacy of the oligonucleotide. The data here establishes the importance of adding Ca2+ and Mg2+ to the formulation for the safety of CNS administration of therapeutic oligonucleotides.

A Solid-State Electrolyte Facilitates Acidic CO2 Electrolysis without Alkali Metal Cations by Regulating Proton Transport.

Electrochemical CO2 reduction (CO2R) in acidic media provides a pathway to curtail CO2 losses by suppressing the formation of (bi)carbonates. In such systems, a high concentration of alkali metal cations is necessary for mitigating the proton-rich environment and suppressing the competing hydrogen evolution reaction. However, a high cation concentration also promotes salt precipitation within the gas diffusion layer, resulting in poor system durability. Here, we resolve this conundrum by replacing the liquid catholyte with a solid-state proton conductor to regulate H+ transport. This is postulated to allow for a locally alkaline environment at the cathode, enabling selective CO2R even without alkali metal cations. We show that this strategy is effective over a broad range of catalyst systems. For instance, we achieve an 87% CO faradaic efficiency (FE) at 300 mA/cm2 using a composite nanoporous Au and single-atom Ni catalyst, with 0.25 M H2SO4 as the anolyte. Stable operation over 110 h and a high single-pass carbon efficiency of 82.8% were also successfully demonstrated. Importantly, we find that this solid-state system is also particularly effective at converting dilute feedstock (5% CO2) with a CO FE of 47.7%, a factor of 16.4 times higher than a conventional system. Our results introduce a simple yet effective design approach for developing efficient acidic CO2R electrolyzers.

Species–soil relationships across Amazonia: Niche specificity and consistency in understorey ferns

AbstractAimsKnowledge about species niches along environmental gradients is needed to understand community assembly and spatial variation in floristic composition and species richness. In Amazonian rainforests, such knowledge is largely lacking, although ferns have been used to infer overall floristic and edaphic patterns. Here we explore fern species distributions along an important edaphic gradient, how narrow their realised niches are and how sensitive inferences are to species commonness, data quality and the region being sampled.LocationAmazonia.MethodsWe used a large data set (1,215 transects across lowland Amazonia) to explore the realised niches of 54 species of two fern genera (Adiantum and Lindsaea) along a soil base cation concentration gradient. We used weighted averaging to estimate species optima and niche widths, and Huisman–Olff–Fresco modelling to assess species response shapes.ResultsOverall, species optima were rather evenly spread along the soil base cation concentration gradient, but Lindsaea optima were limited to the lower half of the gradient, whereas Adiantum optima were more often in the upper half. Most species had unimodal response curves. Mean niche width was ca. 25% of the observed gradient length for Adiantum and 17% for Lindsaea and was only weakly or not at all related to different aspects of species commonness. Species optima were robust to different modelling approaches and consistent across regional subsets. However, the central Amazonian data contained no transects with high soil base cation concentration, so species with high optima were either absent or obtained a lower optimum than in the NW and SW regions.ConclusionsOur results support niche‐related species sorting as an important process that defines species co‐occurrence, turnover and richness patterns within Amazonian rainforests. All Adiantum and Lindsaea species, including the most abundant ones, had narrow enough realised niches to be considered useful indicators of edaphic and floristic variation within the rainforest.

Preventing acute neurotoxicity of CNS therapeutic oligonucleotides with the addition of Ca2+ and Mg2+ in the formulation.

Oligonucleotide therapeutics (ASOs and siRNAs) have been explored for modulation of gene expression in the central nervous system (CNS), with several drugs approved and many in clinical evaluation. Administration of highly concentrated oligonucleotides to the CNS can induce acute neurotoxicity. We demonstrate that delivery of concentrated oligonucleotides to the CSF in awake mice induces acute toxicity, observable within seconds of injection. Electroencephalography (EEG) and electromyography (EMG) in awake mice demonstrated seizures. Using ion chromatography, we show that siRNAs can tightly bind Ca2+ and Mg2+ up to molar equivalents of the phosphodiester (PO)/phosphorothioate (PS) bonds independently of the structure or phosphorothioate content. Optimization of the formulation by adding high concentrations (above biological levels) of divalent cations (Ca2+ alone, Mg2+ alone, or Ca2+ and Mg2+) prevents seizures with no impact on the distribution or efficacy of the oligonucleotide. The data here establishes the importance of adding Ca2+ and Mg2+ to the formulation for the safety of CNS administration of therapeutic oligonucleotides.

The complex effect of dissolved organic carbon on desorption of per- and poly-fluoroalkyl substances from soil under alkaline conditions

Per- and poly-fluoroalkyl substances (PFASs) are contaminants of emerging concern, yet the understanding of factors that control their leaching and release from contaminated soils remains limited. This study aimed to investigate the impact of dissolved organic carbon (DOC) on the release of PFASs—specifically, perfluorohexane sulfonate (PFHxS), perfluorooctane sulfonate (PFOS), and perfluorooctanoic acid (PFOA)from soils contaminated by aqueous film forming foam (AFFF). Batch aqueous leaching experiments were conducted on AFFF-contaminated soils under alkaline solution conditions (pH 9.5, 10.5, and 12) as it enhances leaching of both PFAS and DOC. Leaching of PFOS was significantly increased under alkaline conditions. Although the leaching of PFAS generally increased with pH, PFOS appeared to be more retained under the very alkaline pH conditions used in this study. At the same solution pH, leaching of PFOS and DOC was less in Ca(OH)2 than in NaOH. The retention of PFOS under these conditions may be attributable to the shielding of the negative charge of the soil components and colloids (e.g., DOC and clay minerals) in the leachates and/or the screening of negative charges on head groups of PFOS due to the high concentration of divalent cations. Solution chemistry affected desorption of PFOS more than PFHxS and PFOA. The study highlights that the influence of DOC on PFAS leaching and transport can be very complex, and depends on leachate chemistry (e.g., pH and cation type), PFAS chemistry, the magnitude of PFAS contamination and factors that influence the solid:liquid partitioning of organic carbon in soil.

Polycations as Aptamer-Binding Modulators for Sensitive Fluorescence Anisotropy Assay of Aflatoxin B1.

Fluorescence induced by the excitation of a fluorophore with plane-polarized light has a different polarization depending on the size of the fluorophore-containing reagent and the rate of its rotation. Based on this effect, many analytical systems have been implemented in which an analyte contained in a sample and labeled with a fluorophore (usually fluorescein) competes to bind to antibodies. Replacing antibodies in such assays with aptamers, low-cost and stable oligonucleotide receptors, is complicated because binding a fluorophore to them causes a less significant change in the polarization of emissions. This work proposes and characterizes the compounds of the reaction medium that improve analyte binding and reduce the mobility of the aptamer-fluorophore complex, providing a higher analytical signal and a lower detection limit. This study was conducted on aflatoxin B1 (AFB1), a ubiquitous toxicant contaminating foods of plant origins. Eight aptamers specific to AFB1 with the same binding site and different regions stabilizing their structures were compared for affinity, based on which the aptamer with 38 nucleotides in length was selected. The polymers that interact reversibly with oligonucleotides, such as poly-L-lysine and polyethylene glycol, were tested. It was found that they provide the desired reduction in the depolarization of emitted light as well as high concentrations of magnesium cations. In the selected optimal medium, AFB1 detection reached a limit of 1 ng/mL, which was 12 times lower than in the tris buffer commonly used for anti-AFB1 aptamers. The assay time was 30 min. This method is suitable for controlling almond samples according to the maximum permissible levels of their contamination by AFB1. The proposed approach could be applied to improve other aptamer-based analytical systems.

Competition between Self-Assembly and Phase Separation Governs High-Temperature Condensation of a DNA Liquid.

In many biopolymer solutions, attractive interactions that stabilize finite-sized clusters at low concentrations also promote phase separation at high concentrations. Here we study a model biopolymer system that exhibits the opposite behavior, whereby self-assembly of DNA oligonucleotides into finite-sized, stoichiometric clusters tends to inhibit phase separation. We first use microfluidics-based experiments to map a novel phase transition in which the oligonucleotides condense as the temperature increases at high concentrations of divalent cations. We then show that a theoretical model of competition between self-assembly and phase separation quantitatively predicts changes in experimental phase diagrams arising from DNA sequence perturbations. Our results point to a general mechanism by which self-assembly shapes phase boundaries in complex biopolymer solutions.

Characterization of Lateralite: An Environment Friendly Chemical Additive for Soil Stabilization

The objective of this paper is to determine the chemical composition of Lateralite stabilizer and to characterize Lateralite, stabilizer as a solution for improving the engineering properties of fined grained lateritic and clayey soil for road construction. Oxides and metallic compositions of Lateralite was determined by Atomic Absorption Spectroscopy, AAS, composition of chemical elements of Lateralite stabilizer was determined by X-ray Photoelectron Spectroscopy (XPS) and a quantitative analysis by Scanning Electron Microscopy (SEM) associated with Energy Dispersive X-ray spectroscopy (EDX). The oxide composition of Lateralite as determined by AAS is: Calcium Oxide (63.89%), Silicon Oxide (18.31%), Aluminium Oxide (5.89%), Ferrous oxide (1.67%), Magnesium oxide (1.56%), Sulphur oxide (1.22%), Potassium oxide (0.78%), Sodium oxide (0.41%) and L.O.I 6.27%. The elemental composition analysis by XPS revealed ten (10) elements with Percentage Atomic Concentration, PAC, as: Oxygen (54.33%), Carbon (18.26%), Silicon (9.38%), Calcium (7.56%), Magnesium (4.08%), Aluminium (2.90%), Sodium (2.47%), Ferrous (0.44%), Sulphur (0.31%) and Nitrogen (0.27%) while SEM revealed eleven (11) elements: Oxygen (57.9%), Calcium (21.13%), Silicon (11.08%), Aluminium (4.23%), Ferrous (1.89%), Sulphur (1.07%), Magnesium (1.02%), Sodium (0.99%), Potassium (0.35%), Tin (0.18%) and Barium (0.17%). The three (3) characterization techniques used, (AAS, XPS and SEM) revealed the exchangeable cations in Lateralite are Calcium (7.56%), Magnesium (4.08%), Aluminium (2.90%) and Sodium (2.47%) which are in the ratio 3: 1.65:1.17:1, (Ca2+: Mg2+: Al3+ :Na+). This shows a high concentration and quantity of exchangeable calcium cations over other cations. This will enable the formation of Calcium compounds with very strong and stable inter-particle bonds and a stable Lateralite-stabilized soil mixture.

Response of wheat (Triticum aestivum L.) and cowpea (Vigna unguiculata L.) to foliar wetting with low pH mine waters containing acid-generating metal cations

Acid mine drainage (AMD) contains metals that have detrimental effects on crop growth if present in excess in plant-available form. The use of untreated AMD from coal mines for crop irrigation on strategically limed soils is considered a potential option for mine water management, especially in remote areas without access to water treatment infrastructure. However, leaf scorching and trace element enrichment of plant tissue are of potential concern, as these waters often contain high concentrations of potentially toxic, acid-generating metals (Al3+, Fe2+ and Mn2+) which may cause foliar damage and hyper-accumulate in plant tissue. The objectives of this trial were to quantify any foliar injury and metal accumulation in wheat (Triticum aestivum L.) and cowpea (Vigna unguiculata L.) vegetative material after foliar wetting with simulated AMD enriched with metal cations, and to ascertain if biomass production will be affected. In this trial, crop water requirements were not met through mine water irrigation, as this was only a foliar wetting investigation. Two pot experiments were set up, with wheat grown in the winter and cowpea in the summer season of 2021. Sulphuric acid was used to lower pH to 2, after the addition of low, intermediate and high concentrations of individual acid-generating metal cations, as well as a combination of all three cations. Areal foliar injury was greatest for cowpea (18.7%) with a combination of Al, Fe and Mn at the highest concentration. The crop was not able to recover at this injury level. No injury was recorded in wheat. Both crops accumulated only limited quantities of the metal cations. Calculated hazard quotient for cattle ranged from 0.022 to 0.53, indicating that such fodder would be safe to consume. It is concluded that there are large differences in crop specie susceptibility to leaf scorching after foliar wetting with acidic metal cation-rich mine waters. It is recommended, therefore, that because large volumes of mine water need to be managed, and centre pivot overhead irrigation is likely to be utilized to this end, that studies to screen more species to select crops tolerant to scorching through foliage wetting with mine water irrigation be conducted. Thereafter, studies to better understand root zone effects of irrigation with such waters need to be conducted on species that can tolerate foliar wetting with these waters.

Eco-friendly natural mineral biotite as a cesium adsorbent: Utilizing low-concentration acid and hydrogen peroxide

Biotite, a phyllosilicate mineral, possesses significant potential for cesium (Cs) adsorption owing to its negative surface charge, specific surface area (SSA), and frayed edge sites (FES). Notably, FES are known to play an important role in the adsorption of Cs. The objectives of this study were to investigate the Cs adsorption capacity and behavior of artificially weathered biotite and identify mineralogical characteristics for the development of an eco-friendly geologically-based Cs adsorbent. Through various analyses, it was confirmed that the FES of biotite was mainly formed by mineral structural distortion during artificial weathering. The Cs adsorption capacity is improved by approximately 39% (from 20.53 to 28.63 mg g−1) when FES are formed in biotite through artificial weathering using a low-concentration acidic solution mixed with hydrogen peroxide (H2O2). Especially, the Cs selectivity in Cs-containing seawater, including high concentrations of cations and organic matter, was significantly enhanced from 203.2 to 1707.6 mL g−1, an increase in removal efficiency from 49.5 to 89.2%. These results indicate that FES of artificially weathered biotite play an essential role in Cs adsorption. Therefore, this simple and economical weathering method, which uses a low-concentration acidic solution mixed with H2O2, can be applied to natural minerals for use as Cs adsorbents.

Wooded biocorridors substantially improve soil properties in low-altitude rural benchlands

This study examines soil properties in 30- and 60-year-old agricultural biocorridors and provides a comparative overview with neighbouring farmland. Both mixed and undisturbed soil samples were collected from six farmland/biocorridor study areas to assess a wide spectrum of physical, hydrophysical, chemical and biological soil properties. Biocorridor soils were characterised by higher water retention capacities, porosity, aeration and soil carbon stock, the latter increasing with depth. On the other hand, biocorridor bulk density under forest vegetation cover was lower, indicating progressive soil restoration. Slightly lower soil reactions in biocorridor soils disproved the hypothesis that nutrient-rich soils under biocorridors would form substrates with a high base cation content, leading to soil acidification. Biological activity, expressed through respiration coefficients, was generally low due to unfavourable physical conditions (clayey or silty-clay substrates), with the lowest levels in biocorridors. Nevertheless, biocorridor soil microbiota displayed more effective utilisation of organic matter as a carbon and nitrogen source, with lighter-textured soils tending to show more effective organic matter utilisation after excluding the influence of land use. Our results confirm biocorridors as an important landscape component, contributing to both soil stability and local revitalisation of soil environments and further emphasising their potential as climate-change mitigation tools in their role as carbon sinks.

Activity and Selectivity Modulation of CO2 Electroreductions at Au-Water Interfaces Via Tuning Localcation Concentrations

Electrochemical CO2 reduction reaction (CO2RR) is a promising technique for converting the greenhouse gas CO2 into valuable fuels and chemicals in a clean energy society. To understand the underlying electrocatalytic reaction mechanism from the atomic level, researchers are investigating the role of electrolyte ions, particularly alkali metal cations, in various electrocatalytic reactions including CO2RR. Despite this attention, the impact of alkali metal cations is still a topic of debate, and it remains unclear how cations affect the CO2RR and the competing hydrogen evolution reaction (HER).In this study, explicit cations and water solvents were added to Au-water interfacial models to simulate the pathways of CO2RR and HER. Two cations (K+, Li+, and/or H+) were used in the model system to create similarly charged Au surfaces, and the local concentration of alkali metal cations (AM+) was adjusted by replacing AM+ (K+ and Li+) with H+. The first electron transfer step was considered critical in electrocatalytic reductions, so CO2 activation and water dissociation were evaluated for CO2RR and HER, respectively. Ab initio molecular dynamics (AIMD) simulations with the slow-growth sampling approach (SG-AIMD) were used to simulate the corresponding reaction mechanisms, and kinetic barriers were obtained through thermodynamic integrations. With these Au-water-cations interfacial models, a systematic study was conducted to investigate the mechanism of CO2 activation at Au-water-2AM+, Au-water-1AM+, and Au-water-0AM+ interfaces. These results show that a high concentration of metal cations with 2AM+ promotes CO2 activation through short-range electrostatic interactions between cations and key intermediates.Besides CO2 activation, this study also investigated water dissociation during the competing HER. Contrary to the promotion effect observed in CO2RR, local alkali metal cations were found to suppress water dissociation with a high reaction barrier (Figure 1). This can be attributed to the broken connectivity of the hydrogen bond network at Au-water-2AM+ interfaces. The reaction kinetics can be improved by reducing the metal cation concentration. Notably, K+ was found to have a more pronounced promotion effect than Li+ on CO2 activation, while the opposite suppression effect was observed on HER. By tuning the local alkali metal cation concentration, it is anticipated that the overall performance of CO2RR, including both activity and selectivity, can be engineered. Figure 1

Self-Assembly Nanostructure Induced by Regulation of G-Quadruplex DNA Topology via a Reduction-Sensitive Azobenzene Ligand on Cells.

The control of DNA assembly systems on cells has increasingly shown great importance for precisely targeted therapies. Here, we report a controllable DNA self-assembly system based on the regulation of G-quadruplex DNA topology by a reduction-sensitive azobenzene ligand. Specifically, three azobenzene multiamines are developed, and AzoDiTren is identified as the best G4 binder, which displays high affinity and specificity for G4 DNA. Moreover, the reduction-sensitive nature of the azobenzene scaffold allows AzoDiTren to induce a complete change of the G4 topology in a tissue-specific manner, even at high metal cation concentrations. On this basis, the AzoDiTren-induced G4 conformational switch achieves control of the self-assembly of G4-functionalized DNAs on cells. This strategy enables the regulation of G4 and DNA self-assembly by the bioreductant-responsive ligand.

Effects of cation valence on swelling power, solubility, pasting, gel strength characteristics of potato starch

The objective of this study was to investigate the effects of monovalent, divalent and trivalent cations on the physicochemical properties of potato starch. Cations decreased the water absorption in potato starch granules to cause lower swelling power, especially 0.02–0.04 mmol/g Fe3+ or 0.01–0.04 mmol/g Al3+, but 0.01 mmol/g trivalent cation led more amylose dissolving into the water to cause higher solubility. High concentration of divalent or trivalent cations markedly decreased the viscosity in potato starch paste during further heating and cooling, resulting in the decreases of the trough and finial viscosity, especially 0.04 mmol/g Fe3+. Higher valence of cations decreased the gel strength in potato starch, especially 0.02–0.04 mmol/g Fe3+ or Al3+. Higher valence of cations decreased the starch gel binding with the water and caused lower water holding capacity. In general, a higher valence of cations caused more changes in the physicochemical characteristics of potato starch.

A portable device for quick, on-spot, total arsenic measurement over a wide concentration range in water

It is important from a public health perspective, that an on-spot measurement method can quickly distinguish between water sources both below and above the WHO-allowed level of 10 ppb of arsenic (As) in drinking water, because of its toxicity. To that end, a low-cost, colorimeter-based portable device has been developed that works in conjunction with an optimized concentration of a molybdenum-based sensor reagent as a fast method for As measurement. The device, which consists of an IR LED-phototransistor assembly along with the onboard microcontroller, measures the absorbance of the analyte at a wavelength of 890 nm. The absorbance increases in proportion to As(V) concentration. Reagent optimization in the device allows for a very wide measurement range (6 ppb – 1 ppm) for both As(III) and As(V), and hence As, within 10 min of response time. The limit of detection (LOD) and limit of quantification (LOQ) of the device are 6 and 18 ppb, respectively. The device does not give any interference, even on spiking with high concentrations of other common cations (Fe2+, Ca2+, Zn2+, Mg2+, Cu2+, Cd2+, Na+) and anions (SO42−, NO3−), which can be present in water. Also, phosphate interference, if present, is completely eliminated by using an appropriate amount of amberlite IRA-96 free-base microporous resin. The performance of the developed device was verified with environmental water samples and compared with both UV–VIS spectrophotometer and ICP-MS, showing high accuracy. Overall, this work demonstrates that there is a reliable, on-site method for quantitative measurement of As, across a wide range.

Seasonal variations in the levels of glyphosate in soil, water and crops from three farm settlements in Oyo state, Nigeria

This study investigated the concentration of glyphosate in water (groundwater and surface), soil (top and sub) on cassava and maize farms within 3 farm settlements (Akufo, Ilora and Otiri Ipapo) from Ido, Oyo and Iseyin Local Government Areas of Oyo state, Nigeria. Samples of Top and sub soil were taken from the farms while water was collected from wells (groundwater) and streams (surface water) around each farm settlement using standard methods. Crops (cassava and Maize) samples were collected from each of the selected farm after harvest. The samples were collected over a six-month period to reflect seasonal variation. The glyphosate levels were determined using HPLC-FLD after liquid-liquid extraction technique for water and soxhlet extraction for soil crops The pH, electrical conductivity (EC), total dissolved solids (TDS) values for groundwater were within the WHO limits while values recorded for surface water were above the WHO limits. The phosphate and nitrate values were high in surface water compared to groundwater. High concentration of the exchangeable cations were recorded at the top soil for all the farms with values ranging from 4.0 ± 0.1 to 8.2 ± 0.0 for Ca2+, 2.9 ± 0.0 to 5.1 ± 0.1 for Mg2+, 0.3 ± 0.2 to 0.55 ± 0.0 for Na+, and 0.32 ± 0.0 to 8.2 ± 0.0 for K+. the residual concentration of glyphosate taken from wells and taps (groundwater) were within the maximum concentration of glyphosate in drinking water (0.7 mgL−1). Glyphosate concentrations observed were higher in soil samples from all farm settlements during wet season compared to dry, higher concentrations were also observed in surface water during wet season (August) compared to dry, with Akufo farm settlement having the highest concentrations of 29.40 ± 0.83 mgL−1. The glyphosate residues were also higher in cassava (0.3 ± 0.0 mgKg−1) compared to maize (0.07 ± 0.08 mgKg−1) across each farm settlement. Generally, the higher concentrations observed during wet season in both soil and water samples were as a result of active farm activities during wet season and run off respectively. If herbicide usage is not properly monitored within these settlements, it can pose a threat to aquatic animals and humans around the settlements, thus a sustainable and conservative farming is advised.

Porous cyclopentadiene unit-incorporated graphitic carbon nitride nanosheets for efficient photocatalytic oxidation of recalcitrant organic micropollutants in wastewater

For the purpose of searching for efficient photocatalysts to deal with recalcitrant organic micropollutants in wastewater, here an in-situ supramolecule self-assembly-thermal polymerization strategy is developed to prepare a series of porous cyclopentadiene (CPD) unit-incorporated g-C3N4 ultrathin nanosheets (CCPD-g-C3N4). The CCPD-g-C3N4 demonstrate CPD unit doping level-dependent and remarkably enhanced visible-light photocatalytic oxidation efficiency towards two organic micropollutants, acetaminophen and methylparaben, in which the optimized CCPD-g-C3N4-2 shows 6.1 and 3.5 times higher acetaminophen and methylparaben degradation rate than bulk g-C3N4; moreover, CCPD-g-C3N4-2 is still robust and efficient in the treatment of five mixed organic micropollutants in pharmaceutical wastewater, and the satisfactory micropollutant removal efficiency is obtained in a wide pH window and the presence of high concentrations of inorganic anions and cations as well as dissolved organic matters. Theoretical calculation combined with experimental test reveal that CCPD-g-C3N4 can significantly reduce ecological risk of the target pollutant after the photocatalytic degradation reaction. Such enhanced photocatalytic oxidation efficiency is dominated by the accelerated charge carrier separation dynamics and extended visible-light response region due to the incorporation of CPD units, which finally lead to the generation of abundant reactive oxygen species to degrade and mineralize target micropollutants efficiently.

Use of thermally activated Fenton sludge for Cd removal in zinc smelter wastewater: Mechanism and feasibility of Cd removal

Fenton sludge is a byproduct of the Fenton process that contains large amounts of Fe and Ca. Because of the secondary contamination generated during the disposal of this byproduct, ecofriendly treatment methods are needed. In this study, we used Fenton sludge to remove the Cd discharged from a zinc smelter factory, using thermal activation to enhance the Cd adsorption capacity. Among the various temperatures considered (300–900 °C), the Fenton sludge that was thermally activated at 900 °C (TA–FS–900) adsorbed the highest amount of Cd because of its high specific surface area and high Fe content. Cd was adsorbed onto TA–FS–900 via complexation with C–OH, C–COOH, FeO−, and FeOH and cation exchange with Ca2+. The maximum adsorption of TA–FS–900 was 260.2 mg/g, indicating that TA–FS–900 is an efficient adsorbent, comparable to those reported in the literature. The initial Cd concentration in the zinc smelter wastewater discharged was 105.7 mg/L, 98.4% of which was removed by applying TA–FS–900, suggesting the applicability of TA–FS–900 for real wastewater containing high concentrations of various cations and anions. The leaching of heavy metals from TA–FS–900 was within the EPA standard limits. We concluded that the environmental impact of Fenton sludge disposal can be reduced, and the use of Fenton sludge can add value to the treatment of industrial wastewater in terms of the circular economy and environment.

Metagenomic Analysis of a Concrete Bridge Reveals a Microbial Community Dominated by Halophilic Bacteria and Archaea.

Concrete hosts a small but diverse microbiome that changes over time. Shotgun metagenomic sequencing would enable assessment of both the diversity and function of the microbial community in concrete, but a number of unique challenges make this difficult for concrete samples. The high concentration of divalent cations in concrete interferes with nucleic acid extraction, and the extremely low biomass in concrete means that DNA from laboratory contamination may be a large fraction of the sequence data. Here, we develop an improved method for DNA extraction from concrete, with higher yield and lower laboratory contamination. To show that this method provides DNA of sufficient quality and quantity to do shotgun metagenomic sequencing, DNA was extracted from a sample of concrete obtained from a road bridge and sequenced with an Illumina MiSeq system. This microbial community was dominated by halophilic Bacteria and Archaea, with enriched functional pathways related to osmotic stress responses. Although this was a pilot-scale effort, we demonstrate that metagenomic sequencing can be used to characterize microbial communities in concrete and that older concrete structures may host different microbes than recently poured concrete. IMPORTANCE Prior work on the microbial communities of concrete focused on the surfaces of concrete structures such as sewage pipes or bridge pilings, where thick biofilms were easy to observe and sample. Because the biomass inside concrete is so low, more recent analyses of the microbial communities inside concrete used amplicon sequencing methods to describe those communities. However, to understand the activity and physiology of microbes in concrete, or to develop living infrastructure, we must develop more direct methods of community analysis. The method developed here for DNA extraction and metagenomic sequencing can be used for analysis of microbial communities inside concrete and can likely be adapted for other cementitious materials.