Cation Exchange Research Articles

Efficient Removal of Cu(II) and Ni(II) Ions from Aqueous Solutions Using Reduced Graphene Oxide/Bentonite Clay/ZnO Nanocomposites: Kinetics, Mechanisms, and Adsorption Performance

<p style="text-align:justify;text-indent:36.0pt;"><span style="font-family:"Arial","sans-serif";font-size:11pt;line-height:150%;">To assess the efficacy of removing heavy metals such as Cu (II) and Ni (II) ions from aqueous solution, the adsorption behaviour of a nanocomposite powder comprising of reduced Graphene Oxide (rGO), bentonite clay, and ZnO was investigated. Various analytical techniques including Fourier transform infrared spectroscopy, Field emission scanning electron microscopy, Energy-Dispersive X-ray spectroscopy, X-Ray diffraction analysis, and N<sub>2</sub> adsorption/desorption analysis were utilized to analyse the synthesized composites. Through the batch equilibrium approach, parameters influencing adsorption behaviours, including initial metal ion concentration, pH, adsorbent dosage, and contact time, were comprehensively examined. Adsorption data were shown to have good fit to the Langmuir isotherm model and pseudo-first-order model, with high R<sup>2</sup>, low root mean square error (RMSE), low chi square (Χ<sup>2</sup>), and low standard deviation (SD) values when using the linear regression approach. For the raw sample (rGO/ bentonite clay) containing copper and nickel, equilibrium was achieved in 80 minutes, while for samples with 1% (rGO/ bentonite clay/1% ZnO), 3% (rGO/ bentonite clay/3% ZnO), and 5% (rGO/ bentonite clay/5% ZnO), equilibrium was attained within 70 minutes. </span><span style="background-color:white;font-family:"Arial","sans-serif";font-size:11pt;line-height:150%;">Within the pH range of 2 to 12, the adsorption kinetics of copper and nickel exhibited a notable pH-dependent relationship, highlighting the pronounced influence of pH conditions on the adsorption process</span><span style="background-color:white;color:#374151;font-family:"Segoe UI","sans-serif";font-size:11pt;line-height:150%;">. </span><span style="background-color:white;font-family:"Arial","sans-serif";font-size:11pt;line-height:150%;">Copper consistently demonstrated superior removal efficiency compared to nickel in all conducted adsorption tests, attributed to its heightened propensity for bond formation with adsorbent surfaces.</span><span style="font-family:"Arial","sans-serif";font-size:11pt;line-height:150%;"> The primary pathways for copper and nickel adsorption on the composites involved intermolecular interactions, cation exchange, physisorption and electrostatic interactions. The Langmuir model revealed maximum Cu (II) adsorption capacities of 312.5 mg/g, 217.39 mg/g, 161.95 mg/g, and 101.96 mg/g for raw sample, 1%, 3%, and 5% samples, respectively. Nickel (II) adsorption capacity were measured at 252.41 mg/g, 185 mg/g, 125.03 mg/g, and 96.60 mg/g for the raw sample, 1%, 3%, and 5% samples, respectively.</span></p>

Positive impacts of compost and biochar from orange peel waste on Phaseolus vulgaris physio-biochemistry and productivity and soil properties under salinity stress

ABSTRACT Bioconversion of organic orange peel wastes into compost (OPC) or biochar (OPB) can help overcome the effects of soil salinity and maintain agricultural productivity. Effect of 1.0% OPC or 1.0% OPB as soil amendments on soil properties and performance of Phaseolus vulgaris plants under two salinity levels [5.60 dS m−1 (S-1) and 9.60 dS m−1 (S-2)] versus control [1.60 dS m−1 (S-0)] was investigated. Compared to the control, S-1 and S-2 increased soil sodium ion (Na+) content, while reducing soil organic matter (OM), macro- and micro-nutrients, cation exchange capacity (CEC), and enzyme (urease, acid phosphatase, and alkaline phosphatase) activities, reflecting decreased plant growth and yield. Under S-1 or S-2, OPC application exceeded OPB application, but both considerably enhanced soil OM content, nutrients, CEC, and enzyme activities. These positive results reflected decreased leaf electrolyte leakage and increased leaf-relative water content, pigments, nutrients, K+/Na+ ratio, antioxidant activity, plant growth, and yield. The beneficial impacts of 1.0% OPC were more pronounced under S-2 than S-1 or S-0. In conclusion, adding 1.0% OPC to saline soil (ECe of about 5–10 dS m−1) could mitigate the influences of soil salinity to improve Phaseolus vulgaris growth, physio-biochemistry, and yield.

Investigating the Effects of Elevation on Microbial Communities and Soil Properties at Fanjing Mountain, China

Elevation is one of the most influential factors affecting soil characteristics and microbial communities in forest ecosystems. Nevertheless, there is no consensus on how soil characteristics, soil microbials, and their relationships response to the elevation of the mountain ecosystem. We investigated the soil physicochemical characteristics, the activity of soil enzymes, and the microbial community at elevational sites from 600 to 2400 m above sea level (asl) in the western slopes of the Fanjing Mountain ecosystem, China. The soil microbial communities were determined by high throughput 16S rRNA and ITS amplicon sequencing. The results demonstrated that soil total nitrogen (TN) showed a slight decrease, whereas total phosphorus (TP) and total potassium (TK) gradually tended to increase with increasing elevation. The large macroaggregates (>2 mm) accounted for the largest proportion of the aggregate fraction (66.23%–76.13%) in the 0–10 cm soil layer with elevation. The average values of the soil electrical conductivity (EC), soil organic carbon (SOC), and cation exchange capacity (CEC) concentration in the 0–60 cm layer undulated with increasing elevation, and the highest values were observed at 1500–1800 m asl and 1800–2100 m asl, respectively. The activities of soil urease, sucrase, acid phosphatase, and catalase clearly differed (p < 0.05) with increasing elevation, and the minimum values were found at 2100–2400 m asl. Interesting, with increasing soil depth, the values of these factors tended to decrease, indicating surface aggregation. In addition, the soil microbial (bacterial and fungal) community diversity exhibited a single-peak pattern with elevation. Our results also revealed that the soil bacterial and fungal communities varied significantly at different elevation sites. The bacterial communities were dominated by the phyla Acidobacteria, Pseudomonadota, and Chloroflexi, and the phyla Basidiomycota and Ascomycota dominated the fungal communities. The Pearson and redundancy analyses revealed that the SOC, TP, four soil enzymes, and soil aggregates were significant factors influencing the soil microbial community. In conclusion, soil properties and enzyme activities jointly explained the elevational pattern of the soil microbial community in the Fanjing Mountain. The results of this study provide insights into the influence of elevation on soil characteristics, microbial communities, and their relationships in the Fanjing Mountain ecosystem.

An Experimentally Designed Sertaconazole Sensor for Selective and Enhanced Potentiometric Response: Determination in Cream, Plasma & in Presence of Other Imidazoles

AbstractA two‐step experimental design was followed to develop a potentiometric solid contact ion‐selective electrode for sertaconazole (STN) determination. A full factorial design was first employed in screening for the best cation exchanger, ionophore and conducting polymer. Amounts of the selected cation exchanger; tetrakis[3,5‐bis(trifluoromethyl)phenyl] borate (TFPB), and ionophore; calix[6]arene (CX6), incorporated in STN sensing membrane were then optimized with the aid of face centered composite design. Calibration slope, detection limit and electrode selectivity in presence of another imidazole‐classified drug; econazole, were the selected responses in both designs. The optimized ion‐sensing membrane, containing 1.0 mg TFPB and 9.9 mg CX6, showed enhanced responses compared to the primarily screened ones. This optimized electrode exhibited a linear response over a concentration range of 1.0×10−6‐−1.0×10−3 M with a Nernstian slope of 57.50 mV/decade. The detection limit was lowered by about one order of magnitude via this optimization to equal 3.16×10−7 M. The proposed electrode was successfully challenged for STN determination in the presence of other imidazoles. It was then used for STN determination in cream and spiked plasma as an example of biological fluid. Our proposed potentiometric method was finally compared to the reported chromatographic ones in terms of sensitivity, and greenness evaluation by the widely applicable Analytical GREEnness (AGREE) tool. The comparison revealed the superiority of our method in terms of sensitivity and sustainability.

Improved extraction efficiency of radioactive copper produced via accelerator neutrons method through phosphate buffer-enhanced column pre-treatment

We report a straightforward and robust method for isolating medical copper radioisotopes 64Cu and 67Cu, generated by an accelerator neutrons technique from natZn(n, x). This study reveals the key role of a phosphate buffer pre-treatment of the cation exchange column in the separation process. Incorporating the phosphate buffer into the column pre-treatment markedly enhances the retention of copper isotopes within the column throughout the separation procedure. This approach yields a remarkably high-purity radioactive copper sample with a high extraction efficiency of 94.4 (1.5) % of the initially produced copper, all within a relatively short experimental timeframe of approximately 5 h for 100 g of starting material. This single-step separation scheme is reproducible across a range of starting material target sizes, from small (10 g) to large (100 g). The copper radioisotopes obtained are suitable for use in pre-clinical studies. Thus, this approach offers a more effective means for routine preparation of copper radioisotopes.

Soil nutrient stocks in areas where oiticica (Licania rigida Benth) occurs in the paraiba hinterland

The experiment was conducted in the municipalities of Catolé do Rocha and Pombal, both located in the state of Paraíba in northeastern Brazil. The areas are composed of Eutrophic Fluvic Neosols, with low-activity clay and high natural fertility in flat relief. The factorial arrangement was 2x2, with a completely randomized design, with two municipalities: Catolé do Rocha and Pombal and two soil sampling depths: 0–20 cm and 20–40 cm, selecting 10 matrices of oiticica, L. rigida Benth, representing 10 replicates. In the municipality of Catolé, soil analysis revealed higher SB and CTC with lower pH and MOS compared to the municipality of Pombal. The chemical characterization of the soil in the surface layers presents higher concentrations of nutrients than in the subsurface layers, mainly regarding the levels of MO, reflecting in higher levels of phosphorus, sum of bases and cation exchange capacity.

Water-Mediated Surface Engineering Enhances High-Voltage Stability of Fast-Charge LiCoO2 Cathodes.

Maintaining the surface structure stability of LiCoO2 (LCO) during rapid charge-discharge processes (>5C) and under high-voltage conditions (>4.2 V) is challenging due to interfacial side reactions, cobalt dissolution, and oxygen redox activity at deeply delithiated states, all of which contribute to performance degradation. Herein, different from traditional surface coating methods, we report a water-mediated strategy that modifies the surface architecture of LCO, creating a passivating layer to inhibit surface degradation and enhance cycling stability under fast charging conditions. The surface etching of LCO by H2O is accompanied by a concurrent Li+/H+ cation exchange, which passivates surface oxygen with H+ ions, thereby enhancing both the hydrophobicity and structural stability. Consequently, the modified LCO exhibits superior capacity retention, which is 2.5 times that of the pristine LCO, after 100 cycles at a current density of 1000 mA g-1 (∼6C at 4.5 V). Even at an elevated temperature of 45 °C, it maintains impressive cycling stability at a current density of 500 mA g-1 (∼3C), as demonstrated in practical full-cell configurations. Investigation with multiple samples confirmed that the water-mediated strategy demonstrated broad applicability. We emphasize that the water-mediated modification of the surface architecture on cathode materials offers significant insights into enhancing the stability of high-energy-density lithium-ion batteries (LIBs).

Alternate materials for the capture and quantification of gaseous oxidized mercury in the atmosphere

Abstract. Methodologies for identifying atmospheric oxidized mercury (HgII) compounds, including particulate-bound HgII (HgII(p)) and gaseous oxidized mercury (HgII(g)), by mass spectrometry are currently under development. This method requires preconcentration of HgII for analysis due to high instrument detection limits relative to ambient HgII concentrations. The objective of this work was to identify and test materials for quantitative capture of HgII from the gas phase and to suggest potential surfaces onto which HgII can be collected, thermally desorbed, and characterized using mass spectrometry methods. From the literature, several compounds were identified as potential sorbent materials and tested in the laboratory for uptake of gaseous elemental mercury (Hg0) and HgII(g) (permeated from a HgBr2 salt source). Chitosan, α-Al2O3, and γ-Al2O3 demonstrated HgII(g) capture in ambient air laboratory tests, without sorbing Hg0 under the same conditions. When compared to cation exchange membranes (CEMs), chitosan captured a comparable quantity of HgII(g), while ≤90 % of loaded HgII(g) was recovered from α-Al2O3 and γ-Al2O3. When deployed in the field, the capture efficiency of chitosan decreased compared to CEMs, indicating that environmental conditions impacted the sorption efficiency of this material. The poor recovery of HgII from the tested materials compared to CEMs in the field indicates that further identification and exploration of alternative sorbent materials are required to advance atmospheric mercury chemistry analysis by mass spectrometry methods.

Processing of Sludge Water from Alumina Production by Electrodialysis

The possibility of using the electrodialysis for processing weak aluminate solutions (sludge water) for the purpose of their concentration and causticization is analyzed. For testing, a three-chamber electro-dialysis cell with heterogeneous cation exchange membranes MK-40 was used. The optimal operating parameters of the process were determined, as follows: pole-to-pole distance 3–4 cm and current density 2 A/dm2 at the operating voltage on the cell of 20–26 V. Specific electricity consumption was established as 9.7–20.6 kWh/kg alkali, causticization efficiency 56.1–69.6%, alkali yield – 81%.

Kinetics of Cd adsorption by biochar, activated carbon, and zeolite in some calcareous soils

AbstractDifferent methods have developed to reduce the risks of potentially toxic elements in contaminated soils. Among them, adsorption is one of the most important and effective strategies. In this research, kinetics of Cd adsorption by biochar, activated carbon, and zeolite in some calcareous soils were investigated. A factorial experiment was conducted based on a completely randomized design with three replications. The factors included three types of adsorbents (sunflower's biochar, activated carbon, and zeolite), four levels of Cd (0, 20, 50, and 100 mg/L as Cd (NO3)2), and three soil samples, differing in their cation exchange capacity, soil organic matter, and calcium carbonate equivalent. Batch experiments were carried out to evaluate Cd adsorption isotherms and kinetic models. Furthermore, the effect of adsorbent dosage, contact time, and initial pH on the adsorption efficiency was examined. Optimizing studies revealed that the best pH for Cd adsorption was 5, while the optimal equilibrium time was achieved at 24 h. The results showed that the Freundlich model fitted to the experimental data slightly better than the Langmuir model. Moreover, the pseudo‐second‐order kinetic model better described the kinetic behavior of Cd adsorption for the investigated adsorbents. The maximum Cd removal efficiency (99%) belonged to soil No. 2 with biochar. Lastly, it was concluded that sunflower biochar, a cheap and cost‐effective adsorbent, had high efficiency in Cd adsorption in calcareous soils.

Ultra-Thin Cation Exchange Membranes: Sulfonated Polyamide Thin-Film Composite Membranes with High Charge Density

Ultra-Thin Cation Exchange Membranes: Sulfonated Polyamide Thin-Film Composite Membranes with High Charge Density

Soil Acidification and Its Temporal Changes in Tea Plantations of Guizhou Province, Southwest China

ABSTRACTSoil acidification is a significant problem in intensive agricultural systems, particularly in tea plantations. Guizhou province, located in the center of the karst mountainous region of southwest China, has the largest tea plantation area in China. However, the soil acidification characteristics in the tea plantations of Guizhou province, as well as their temporal changes, have not yet been adequately studied. Therefore, soil acidification and associated soil properties in the major tea‐planting counties of Guizhou province were extensively assessed, and the temporal changes in soil acidity over the past 11 years were also evaluated through long‐term and short‐term experiments. The results showed that the average soil pH in the tea plantations in Guizhou province varied from 4.08 to 4.87, with a mean of 4.47. The average cation exchange capacity (CEC), TEA (total exchangeable acidity, TEA), EH (exchangeable H+), and EA (exchangeable Al3+) values were 9.6, 3.7, 5.8, and 19.0 cmol/kg, respectively. Seasonal changes in tea plantation soil pH were observed in low‐ and moderately acidic soils but not in highly acidic soils. The soil pH values did not significantly change during three consecutive years of in situ observations but significantly decreased over the past 11 years at an average of 0.03 yearly. Correlation analysis revealed that the soil pH in tea plantations was significantly positively correlated with the content of specific amino acids, such as glutamic acid, arginine, and valine, but was significantly negatively correlated with certain soil physicochemical properties. The findings of this study indicate that soil acidification in tea plantations of the Guizhou province is severe and possesses distinctive attributes that should be considered for its effective management.

Multiphase flow and reactive transport benchmark for radioactive waste disposal

AbstractCompacted bentonite is part of the multi-barrier system of radioactive waste repositories. The assessment of the long-term performance of the barrier requires using reactive transport models. Here we present a multiphase flow and reactive transport benchmark for radioactive waste disposal. The numerical model deals with a 1D column of unsaturated bentonite through which water, dry air and $${\hbox {CO}_{2{(g)}}}$$ CO 2 ( g ) may flow and with the following reactions; aqueous complexation, calcite and gypsum dissolution/precipitation, cation exchange and gas dissolution. INVERSE-FADES-CORE V2, $$\hbox {DuMu}^X$$ DuMu X , TOUGHREACT and iCP were benchmarked with 6 test cases of increasing complexity, starting with conservative tracer transport under variably unsaturated conditions and ending with water flow, gas diffusion, minerals and cation exchange. The solutions of all codes exhibit similar trends. Small discrepancies are found in conservative tracer transport due to differences in hydrodynamic dispersion. Computed $${\hbox {CO}_{2{(g)}}}$$ CO 2 ( g ) pressures agree when a sufficiently refined grid is used. Small discrepancies in $${\hbox {CO}_{2{(g)}}}$$ CO 2 ( g ) and pH are found near the no-flow boundary at early times which vanish later. Discrepancies are due differences in the formulations used for gas flow at nearly water-saturated conditions. Computed $${\hbox {CO}_{2{(g)}}}$$ CO 2 ( g ) pressures show a fluctuation between $$10^{-4}$$ 10 - 4 and $$10^{-3}$$ 10 - 3 years which slows down the in-diffusion of $${\hbox {CO}_{2{(g)}}}$$ CO 2 ( g ) . This fluctuation is associated with chemical reactions involving $${\hbox {CO}_{2}}$$ CO 2 . There are discrepancies in solute concentrations due to differences in the Debye–Hückel (DH) formulation. They are overcome when all codes use the same DH formulation. The results of this benchmark will contribute to increase the confidence on multiphase reactive transport models for radioactive waste disposal.

An injectable dual-layer chitosan-alginate nano-hydrogel incorporated Cu(I)-isopolymolybdate-based metal-organic framework tailored for three-in-one anti-cancer nanotherapy

Designing potential agents and constructing hydrophilic nano-hydrogel platforms for biomedical and pharmaceutical applications, especially for polyoxometalate-based metal-organic frameworks (PMOF), present both great desirability and significant challenges. A unique open porous Cu(I)-isopolymolybdate-based metal-organic framework (CCUT) has been self-assembled through ionothermal processes for in vivo synergistic anti-cancer therapy. The periodicity of Drugs@CCUT-1 (nano-crystals of CCUT after cation exchange and anti-cancer drugs upload) has been investigated by synchrotron wide-angle X-ray scattering, confirming the lattice structure unchanged. To mitigate toxicity, enhance stimuli-responsive drug delivery, hydrophilicity, and biocompatibility, an injectable dual-layer chitosan//alginate-based nano-hydrogel is developed to incorporate Drugs@CCUT-1. Potential interactions between the chitosan layer and the surface of CCUT-1 have been analyzed by Density Functional Theory (DFT). Furthermore, the nanoparticles Drugs@CCUT-1@Gel exhibit efficient type I photodynamic therapy (PDT) and chemodynamic therapy (CDT) within the bio-window, effectively eradicating tumors in deep tissue. CCUT-1 generates a substantial amount of reactive oxygen species (ROS), stimulating the Keap1-Nrf2 signaling pathway and resulting in the expression of phase II enzymes, typically HO-1. CCUT-1@Gel not only demonstrates high capacity for anti-cancer drug upload and release, but also exhibits strong synergistic CDT/PDT in vivo anti-tumor efficacy. Hence, CCUT-1@Gel represents a promising in vivo nano-platform for synergistic chemotherapy (CT)/CDT/PDT three-in-one anti-cancer approach.

Lightweight aggregates produced from low-temperature sintering of multiple solid wastes for heavy metals removal: Adsorption kinetics and stabilization

Solid wastes, including incinerated sewage sludge ash (ISSA), waste bentonite, and waste glass powder (WGP), were recycled and sintered at a low temperature (680°C) to produce lightweight aggregates (WSA). WGP acted as a fluxing agent to significantly lower sintering temperature of 1000-1200°C in other studies. WSA demonstrated an excellent mechanical strength of 3.76 MPa. The adsorbent dosage, initial pH, kinetics and isotherm on heavy metals adsorption were evaluated in batch adsorption experiments. The isothermal data exhibited a good correlation with the Langmuir model, and the maximum adsorption capacity was approximately 9.26 mg/g at 296 K. Pb(II) removal was dominated by precipitation and cation exchange. Breakthrough curves were determined for fixed-bed adsorption. At 50% breakthrough, the maximum adsorption capacity was 1.82 mg/g. The WSA after heavy metals adsorption were then reused to replace river sand (10-50%) in producing lightweight mortars. The solidification of spent WSA in the lightweight mortars could significantly reduce the leaching of Pb(II) by 98.5%. Moreover, the reuse of spent WSA resulted in low density and low thermal conductivity of cement mortars. This study demonstrates total waste management for municipal solid wastes: upcycling of waste–utilization–permanently stored as construction materials.

Identifying hidden factors influencing soil Olsen-P in an alkaline calcareous soil using machine learning and geostatistical techniques

Phosphorus (P) deficiency is one of the major constraints for sustainable crop production in calcareous soils. This study aimed to elucidate the key soil characteristics modulating the variability of soil Olsen P in these typical soils. A comprehensive soil sampling initiative (1.5 samples per hectare) was conducted on a 100-hectare farm, considering 31 attributes that included soil physical and chemical properties, and geographic attributes. Three machine learning algorithms—partial least square regression (PLSR), random forest (RF), and cubist regression (CR)—were employed to understand key variables controlling soil Olsen P. Furthermore, the same data set was used to spatially map the variations in Olsen P levels using ordinary kriging. The results revealed that soil chemical factors, specifically exchangeable manganese and zinc, cation exchange capacity, and carbonate, played a crucial role in controlling P levels. Among the machine learning models, the best performing model was RF (R2= 0.95, RMSE= 1.30 mg kg-1) followed by CR (R2= 0.92 and RMSE= 1.43 mg kg-1). Additionally, the analysis using a Gaussian semi-variogram model showed a good performance (R2= 0.78, RMSE = 2.05 m) in visualizing the spatial distribution of Olsen P, revealing its heterogeneity. The resulting pattern of Olsen P distribution may be attributed not only to soil properties but also to external factors, such as sediment transport through watercourses across the study area and atmospheric deposition from a nearby P mining. Overall, the combination of geostatistical methods and machine learning approach demonstrates a significant potential in understanding the complexity of soil available P (Olsen-P)that could help to develop sustainable and precise P management.

The Role of Cation Exchange Membrane Characteristics in CO2 Electrolysis to CO Using Acid Anolyte

Cation exchange membranes are considered a suitable option for zero-gap CO2 electrolysis due to their potential to avoid carbonation and improve carbon efficiency. However, the use of acidic anolytes remains an issue due to high hydrogen production. This study investigates Nafion® membranes (111, 112, 115, 211, and 212) with different thicknesses produced by extrusion or solution-cast processes in a zero-gap cell with an acidic anolyte containing K2SO4. Faradaic efficiencies for CO production (FECO) are higher with thinner membranes, regardless of the manufacturing process, reaching FECO around 75% at 50 mA cm⁻². Additionally, membranes with similar thicknesses (∼50.8 µm) but produced in different ways displayed flow field carbonation after 3 hours of electrolysis at 30°C and 50 mA cm⁻². Linear sweep voltammetry (LSV) in full and half-cell configurations shows limiting diffusion current (iL) relative to proton transport for all the employed membranes, no matter the thickness. In contrast, the iL for Nafion® 115, the thicker membrane, is suppressed, indicating that proton depletion is fast and the electrode surface alkalinization primarily results from water reduction in this case. A mechanistic analysis was performed to explain the behavior of the limiting currents in the cell with Ar- and CO2-feed, indicating that CO2 reduction aids in the consumption of H+ provided by the membrane, increasing the local pH at less negative potentials. Overall, thinner membranes exhibited higher values of FECO and energy efficiency for CO (EE%CO). However, solution-cast membranes are more prone to provide K+, leading to better performance than those prepared by extrusion.

Subsurface drainage and nitrogen management affects soil properties in upstate Missouri U.S.

Enhanced efficiency nitrogen (N) fertilizer management may reduce environmental N losses and increase grain yields. The effect of N fertilizer management practices on soil properties is uncertain. In this 5-year study, we evaluated different N fertilizer management [non-treated control (NTC), fall applied anhydrous ammonia (AA) 190 kg N ha−1 with nitrapyrin (fall AA + NI), preplant AA at 190 kg N ha−1 (spring AA), top-dressed urea (TD urea) as 42 kg N ha−1 SuperU and 126 kg N ha−1 ESN as a 25:75 % granular blend] practices in free drained (FD) and non-drained (ND) soils for their impact on soil properties. In FD soils, N fertilization significantly (P > 0.05) increased soil pH, CEC, cations, and Bray I P compared to the NTC. Improved soil aeration and increased plant growth with TD urea and spring AA fertilizer treatments in FD soils increased soil organic matter (OM) 10–13 % and total organic carbon (TOC) 27–35 % compared to the NTC. Increased clay content and reduced silt content were observed in FD soils with N fertilizer treatments compared to NTC. However, fertilizer applications in ND soils had no effect on soil properties. Increased crop production with FD and 4R N fertilizer applications can improve soil properties with increased soil OM and TOC content. This suggests that a synergetic effect of N fertilization and soil drainage can improve soil health by increasing soil cation exchange capacity (CEC), OM, and TOC content.

Au/Ag@ZnS yolk-shell photocatalysts enhanced with noble metals and hyaluronic acid for efficient hydrogen production in rheumatoid arthritis therapy

Rheumatoid arthritis, characterized by the abnormal proliferation of synovial cells and extensive macrophage infiltration, is a chronic inflammatory disease. Molecular hydrogen, known for its antioxidant properties, has shown promise in eliminating reactive oxygen species. However, the low solubility and bioavailability of hydrogen limit the effectiveness of this therapy. To overcome these issues, we developed a novel yolk-shell heterostructure, H-AAZS (Au/Ag@ZnS modified hyaluronic acid), utilizing a hydrothermal cation exchange process. Through ion doping, semiconductor hybridization, and Schottky barriers in H-AAZS, photocatalysis for hydrogen generation has been successfully implemented using 660 nm laser irradiation. Additionally, the H-AAZS demonstrate the capacity for mild photothermal therapy, inducing apoptosis in synovial cells with Au's hot electrons with 660 nm laser irradiation. This strategy not only improves the abnormal proliferation of synovial cells but also avoids the exacerbation of inflammation caused by thermal stimulation. Both in vitro and in vivo experiments validate the synergistic effects of hydrogen production mediated anti-inflammatory responses, macrophage polarization and photothermal therapy. Therefore, this work represents a significant advancement as it ingeniously harnesses photocatalysis to modulate the synovial microenvironment while mitigating the side effects associated with photothermal therapy. This nanocrystal provides new and valuable insights into the potential treatment of Rheumatoid arthritis.

Cation exchange resin coupled with bacterial pretreatment to promote waste activated sludge reduction: Performance and mechanism

Due to the rapid advancement of industrialization and urbanization, there has been a significant rise in the generation of industrial wastewater and domestic wastewater, which results in the rapid increase of waste activated sludge (WAS). However, the complex structure and slow hydrolysis of sludge limit aerobic digestion of WAS. This study evaluated the effect of lysozyme-secreting strain Proteus mirabilis sp. SJ25 and the new isolation of surfactant-secreting strain Enterobacter cloacae sp. WH11 on the promotion of sludge hydrolysis, and introduced cation exchange resin (CER) to enhance the promotion effect. The reduction efficiencies of suspended solids (SS) and volatile suspended solids (VSS) enhanced by 25.0 and 24.9 %, respectively, and the soluble chemical oxygen demand (SCOD) release was increased by 2370.27 mg/L when the inoculum of strain SJ25 and strain WH11 were 3 % and 6 %, and the dosage of CER was 2.0 g/g SS against the control. The fluorescence region integral (FRI) results showed a significant quantity of dissolved organic matter (DOM) was let out, and the biodegradability of the sludge was improved. The alterations in several physicochemical characteristics of the sludge also suggested that the extracellular polymeric substances (EPS) were disrupted and an enormous quantity of sludge cells were lysed. In addition, functional gene prediction from the Kyoto Encyclopedia of Genes and Genomes (KEGG) database indicated that CER coupled with bacterial pretreatment enhanced microbial metabolic capacity. This work suggests a novel pathway for the development of novel pretreatment methods to promote sludge hydrolysis.