Search Results (253)

This study evaluates and compares the sorption performance of natural zeolite (NZ) and Fe(III)-modified zeolite (FeZ) in removing Cu(II) ions from aqueous solutions, with the goal of assessing their potential for environmental remediation. NZ was modified with Fe(NO₃)₃, NaOH and NaNO₃ solutions to improve its sorption properties. The modification led to a slight decrease in crystallinity (XRD), increase in pore volume (BET), functional groups (FTIR) and negative surface charge (zeta potential), thereby improving the affinity of FeZ towards Cu(II). Batch sorption experiments were conducted to optimize key parameters including pH, solid/liquid ratio (S/L), contact time, and initial Cu(II) concentration. The pH_o and S/L ratio were identified as key factors significantly influencing Cu(II) sorption on both zeolites, with a particularly pronounced effect observed for FeZ. The optimal conditions determined were pH_o = 3–5 for NZ, pH_o = 3 for FeZ, S/L = 10 g/L and a contact time of 600 min. Experimental results confirmed that FeZ has almost twice the sorption capacity for Cu(II) compared to NZ (0.271 mmol/g vs. 0.156 mmol/g), as further supported by elemental analysis, SEM-EDS and mapping analysis of saturated samples. The sorption of Cu(II) followed a mechanism of physical nature driven by ion exchange, dominated by intraparticle diffusion as the rate-controlling step. Leaching of copper-saturated zeolites according to the standard leaching method, DIN 38414 S4, demonstrated the ability of both zeolites to fully retain Cu(II) within their structure over a wide pH range, 4.01 ≤ pH_o ≤ 10.06. These findings highlight the superior performance of FeZ and its potential as an effective material for the remediation of copper-contaminated environments. Full article

In this work, the biosorption potential of Spirulina sp. as an effective and eco-friendly biosorbent for the removal of Ni(II) and Pb(II) ions from aqueous solutions was investigated. Detailed characterization of the biosorbent was carried out, including surface morphology, chemical composition, particle size, zeta potential, crystallinity, zero-point charge, and functional group analysis. Batch tests were performed to determine the kinetic constants and adsorption equilibrium of the studied ions. The adsorption behavior of Spirulina sp. was described using six adsorption isotherms. The best fit was obtained for the Redlich-Peterson and Langmuir isotherms, indicating that monolayer adsorption occurred. The maximum biosorption capacities for Ni(II) and Pb(II) were 20.8 mg·g⁻¹ and 93.5 mg·g⁻¹, respectively, using a biosorbent dose of 10 g·L⁻¹, initial metal concentrations ranging from 50 to 5000 mg·L⁻¹, at pH 6, 20 °C, and a contact time of 120 min. Low values of the mean free energy of adsorption (E) in the Dubinin–Radushkevich and Temkin model (0.3 and 0.1 kJ·mol⁻¹ for Pb(II) and 0.35 and 0.23 kJ·mol⁻¹ for Ni(II)) indicate the dominance of physical processes in the ion binding mechanism. The adsorption of Pb(II) ions was more effective than that of Ni(II) ions across the entire range of tested concentrations. At low initial concentrations, the removal of Pb(II) reached 94%, while for Ni(II) it was 80%. Full article

Surfactants are widely utilized in agriculture as emulsifying, dispersing, anti-foaming, and wetting agents. In these adjuvant roles, the inherent biological activity of the surfactant is secondary to the active ingredients. Here, the hydrophilic non-ionic surface-active tri-block copolymer Pluronic^® F68 is investigated for direct biological activity in wheat. F68 binds to and inserts into lipid membranes, which may benefit crops under abiotic stress. F68’s interactions with Triticum aestivum (var Juniper) seedlings and a seed-borne Bacillus spp. endophyte are presented. At concentrations below 10 g/L, F68-primed wheat seeds exhibited unchanged emergence. Root-applied fluorescein-F68 (fF68) was internalized in root epidermal cells and concentrated in highly mobile endosomes. The potential benefit of F68 in droughted wheat was examined and contrasted with wheat treated with the osmolyte, glycine betaine (GB). Photosystem II activity of droughted plants dropped significantly below non-droughted controls, and no clear benefit of F68 (or GB) during drought or rehydration was observed. However, F68-treated wheat exhibited increased transpiration values (for watered plants only) and enhanced shoot dry mass (for watered and droughted plants), not observed for GB-treated or untreated plants. The release of seed-borne bacterial endophytes into the spermosphere of germinating seeds was not affected by F68 (for F68-primed seeds as well as F68 applied to roots), and the planktonic growth of a purified Bacillus spp. seed endophyte was not reduced by F68 applied below the critical micelle concentration. These studies demonstrated that F68 entered wheat root cells, concentrated in endosomes involved in transport, significantly promoted shoot growth, and showed no adverse effects to plant-associated bacteria. Full article

Automated parcel lockers (APLs) are transforming urban last-mile delivery by reducing failed distributions, decoupling delivery from recipient availability, optimizing carrier routes, reducing carbon foot-print and mitigating traffic congestion. The paper investigates the optimal design of APLs systems under stochastic demand and operational constraints, formulating the problem as a resource allocation optimization with service-level guarantees. We proposed a data-driven discrete-event simulation (DES) model implemented in ARENA to (i) determine optimal locker configurations that ensure customer satisfaction under stochastic parcel arrivals and dwell times, (ii) examine utilization patterns and spatial allocation to enhance system operational efficiency, and (iii) characterize inventory dynamics of undelivered parcels and evaluate system resilience. The results show that the configuration of locker types significantly influences the system’s ability to maintain high customers service levels. While flexibility in locker allocation helps manage excess demand in some configurations, it may also create resource competition among parcel types. The heterogeneity of locker utilization gradients underscores that optimal APLs configurations must balance locker units with their size-dependent functional interdependencies. The Dickey–Fuller GLS test further validates that postponed parcels exhibit stationary inventory dynamics, ensuring scalability for logistics operators. As a theoretical contribution, the paper demonstrates how DES combined with time-series econometrics can address APLs capacity planning in city logistics. For practitioners, the study provides a decision-support framework for locker sizing, emphasizing cost–service trade-offs. Full article

A substrate–product switch model was proposed to describe ethanol fermentation from longan solid waste using Candida tropicalis at an initial glucose and xylose ratio of 2 to 1. The model incorporated multiple rate equations for cell growth, sugar uptake, and ethanol production along with ethanol consumption. It elucidated the following three-step mechanism: (I) sugar uptake, (II) sugar conversion, and (III) ethanol consumption concerning the effects of concentration factor (CF) and associated growth function. Optimal kinetic parameters were estimated and validated against experimental data. The identification of two critical xylose concentrations showed that ethanol consumption either preceded or coincided with xylose consumption cessation. The phenolics inhibitory effect of gallic acid, ellagic acid, pyrogallol, and catechol on cell growth and ethanol production was elucidated with relatively minimal effect. The highest ethanol concentration of 25.5 g/L was reached with corresponding ethanol mass yield and productivity of 0.30 g/g and 1.063 g/L/h, respectively. The proposed model and kinetics provide valuable insights for designing and optimizing ethanol fermentation, contributing to more sustainable and cost-effective ethanol production. Full article

Heavy metal pollution, especially from Pb(II) and Cd(II), poses significant risks due to its persistence and bioaccumulation potential. Traditional removal methods face challenges like high costs and secondary pollution. This study developed a novel three-dimensional porous adsorbent XBS, derived from xanthate-modified Phanerochaete sordida YK-624 (a white-rot fungus), for the rapid and efficient removal of Pb(II) and Cd(II) from wastewater. Characterization showed that XBS has a sponge-like structure with abundant functional groups, significantly enhancing its adsorption capacity and kinetics. XBS achieved 96% Pb(II) and 32% Cd(II) removal within 1 min at a 0.25 g/L dose, reaching over 95% of the maximum adsorption capacity within 30 min for Pb(II) and 240 min for Cd(II). The maximum capacities were 224.72 mg/g for Pb(II) and 82.99 mg/g for Cd(II). Kinetic and thermodynamic analyses indicated a chemisorption-driven process, which was both endothermic and spontaneous. XBS exhibited high selectivity for Pb(II) over Cd(II) and other metals (Tl(I), Cu(II)), attributed to stronger covalent interactions with sulfur- and nitrogen-containing groups. Mechanistic analyses (XRD, FTIR, and XPS) revealed that removal occurs via ion exchange, complexation, and precipitation, forming stable compounds like PbS/CdS and PbCO₃/CdCO₃. Given its cost-effectiveness, scalability, and high efficiency, XBS represents a promising adsorbent for heavy metal remediation, particularly in Pb(II)-contaminated wastewater treatment applications. Full article

To promote environmentally sustainable remediation and resource recovery from ion-adsorption rare earth tailings (IRET), this study comprehensively investigated the previously isolated strain REO-01 by examining its sulfate-reducing performance, Cd(II) immobilization potential, and physiological and biochemical responses under varying environmental conditions. Strain REO-01 was identified as a Gram-negative facultative anaerobe with strong sulfate-reducing activity and effective Cd(II) immobilization capacity. During a 96 h incubation period, the strain entered the exponential growth phase within 36 h, after which the OD₆₀₀ values plateaued. Concurrently, the culture pH increased from 6.83 to 7.5, and the oxidation-reduction potential (ORP) declined to approximately −300 mV. Cd(II) concentrations decreased from 0.2 mM to 3.33 μM, corresponding to a removal efficiency exceeding 95%, while sulfate concentrations declined from 1500 mg/L to 640 mg/L, with a maximum reduction efficiency of 66.16%. The strain showed optimal growth at 25–40 °C and near-neutral pH (6–7), whereas elevated Cd(II) concentrations (≥0.2 mM) significantly inhibited cell growth. A sulfate concentration of 1500 mg/L was found to be optimal for cellular activity. Among the tested carbon sources, sodium lactate at 4.67 g/L yielded the most favorable results, reducing ORP to −325 mV, increasing pH to 7.6, and lowering Cd(II) and sulfate concentrations to 3.33 μM and 510 mg/L, respectively. These findings highlight the strong potential of strain REO-01 for simultaneous sulfate reduction and Cd(II) remediation, supporting its application in the in situ bioremediation and resource utilization of rare earth tailings. Full article

This study investigates the adsorption and desorption efficiencies of Cu (II) and Cd (II) from industrial effluents using orange peel powder and a newly developed mixed adsorbent composed of equal parts of activated charcoal (AC) and bone charcoal (BC). The mixed adsorbent (AC + BC) exhibited significantly higher removal efficiencies for both copper and cadmium metal ions compared to orange peel powder. This can be attributed to the high surface area of AC and the negative surface charge of BC, resulting in a synergistic adsorption effect. Batch adsorption experiments were conducted in an orbital shaker at 150–180 rpm for 60 min, followed by thorough rinsing to remove any residual metal ions. The optimal pH for maximum adsorption of Cu (II) and Cd (II) was found to be 6. The effects of adsorbent dosage (ranging from 0.5 to 5 g/L) and contact time (ranging from 15 min to 4 h) on adsorption performance were systematically studied. Regeneration experiments using 0.2 M HCl demonstrated that the adsorption of Cu (II) and Cd (II) on the mixed adsorbent was highly reversible, achieving desorption efficiencies of 90% and 94%, respectively. Notably, Cd (II) consistently exhibited higher desorption rates across all tested dosages. These results confirm the potential of the proposed adsorbent and regeneration strategy for efficient and economical removal of heavy metals from industrial wastewater. Full article

Background: Iron deficiency (ID) is a commonly seen comorbidity in heart failure (HF) patients. It is often associated with a poor prognosis and impaired physical capacity. The functional limitations linked to ID may lead to cardiac function abnormalities. The functional limitations linked to ID may lead to cardiac function abnormalities, that can be reversible after iron repletion. Some echocardiographic parameters, such as global longitudinal strain (GLS), myocardial work (MW) and its derivatives constructive work (CW), wasted work (WW) and work efficiency (WE), may be of added value in advanced cardiac performance assessment. Methods: IRON-PATH II was a multicenter, prospective and observational study designed to describe the pathophysiological pathways associated with ID. The echo-substudy included 100 HF patients that had undergone a specific pilot echocardiographic evaluation. Patients had a left ventricular ejection fraction (LVEF) ≤50%, were in stable clinical condition and on standard HF medication with hemoglobin ≥11 g/dL. The final cohort included 98 patients. Results: The ID group showed worse cardiac function, with lower GLS (−8.5 ± 9% vs. −10 ± 10%), WE (74 ± 10% vs. 80 ± 10%) and MW (665 [453–1013] vs. 947 [542–1199] mmHg%), as well as higher WW (290 [228–384] vs. 212 [138–305] mmHg%) and lower RV free wall strain (−13 [−20–(−11)]% vs. −17 [−23–(−14)]%). Following iron repletion, ID patients demonstrated improved LV (GLS, MW, WE and WW) and RV performance (RV free wall strain), aligning with non-ID patients (all p-values >0.05 compared to the non-ID group). Conclusions: Among HF patients with reduced LVEF, ID was associated with worse myocardial performance in both the LV and RV. All the alterations seen were reversible after intravenous iron repletion. Full article

The contamination of natural waters with heavy metals is a global problem. Biosorption is an environmentally friendly and effective technology that offers advantages when metals are present in low concentrations. It also facilitates the recovery and conversion of metals, which are valuable resources. The removal capacity of Ag(I) and Zn(II) ions by Staphylococcus epidermidis CECT 4183 and the ability of its cell extract to synthesize Ag/AgCl and ZnO nanoparticles were investigated. Their biocidal capacity was evaluated. The factors involved were optimized and the mechanisms were studied. The optimal conditions for Ag(I) biosorption were pH 4.5 and a biomass dose of 0.8 g/L. For Zn(II), the biomass dose was 0.2 g/L and pH 4.2. A maximum biosorption capacity (Langmuir model) of 47.43 and 65.08 mg/g, respectively, was obtained. The cell extract promoted the synthesis of Ag/AgCl and ZnO nanoparticles with average sizes below 35 nm. The ZnO nanoparticles exhibited excellent inhibitory properties against planktonic cells of five microbial strains, with MIC values ranging from 62.5 to 250 µg/mL. Their response to biofilms remained between 70% and 100% inhibition at low concentrations (125 µg/mL). The studied bacteria show potential to remove heavy metals and promote the environmentally friendly synthesis of biocidal nanoparticles. Full article

This study investigates the potential of biochars derived from agricultural waste biomass for the removal of heavy metal ions from aqueous solutions. Biochars were produced via slow pyrolysis at 793 K using almond shells (AS), walnut shells (WS), pistachio shells (PS), and rice husks (RH) as feedstocks. The physicochemical properties and adsorption performance of the resulting materials were evaluated with respect to Cd(II), Mn(II), Co(II), Ni(II), Zn(II), total Iron (Fe_tot), total Arsenic (As_tot), and total Chromium (Cr_tot) in model solutions. Surface morphology, porosity, and surface chemistry of the biochars were characterized by scanning electron microscopy (SEM), nitrogen adsorption at 77 K (for specific surface area and pore structure), Fourier-transform infrared spectroscopy (FTIR), and determination of the point of zero charge (pH_pzc). Based on their textural properties, biochars derived from WS, PS, and AS were classified as predominantly microporous, while RH-derived biochar exhibited mesoporous characteristics. The highest Brunauer–Emmett–Teller (S_BET) surface area was recorded for PS biochar, while RH biochar showed the lowest. The pistachio shell biochar exhibited the highest specific surface area (440 m²/g), while the rice husk biochar was predominantly mesoporous. Batch adsorption experiments were conducted at 25 °C, with an adsorbent dose of 3 g/L and a contact time of 24 h. The experiments in multicomponent systems revealed removal efficiencies exceeding 87% for all tested metals, with maximum values reaching 99.9% for Cd(II) and 97.5% for Fe_tot. The study highlights strong correlations between physicochemical properties and sorption performance, demonstrating the suitability of these biochars as low-cost sorbents for complex water treatment applications. Full article

The lactic acid (LA) production from corn stover using Lewis acid catalysts was optimized. Initially, an equimolar mixture of Al(III)/Sn(II) was used as a catalytic system at 190 °C with 5 wt% biomass. Increasing the catalyst concentration led to higher LA production, showing the optimal results at 16 mM. A low catalyst concentration mainly produced furfural and HMF, dehydration products from the corn stover sugars. Higher catalyst concentration increased LA yield but also produced the degradation of the glucose dehydration products into levulinic and formic acids, reducing LA selectivity. Al(III) was essential for LA formation, while Sn(II) was less effective due to its lower solubility, shown by the presence of Sn(II) in the solid residue after treatments. A total of 16 mM Al(III) yielded the highest LA levels at 190 °C, 7.4 g/L, and 20.7% yield. Increasing the temperature to 210 °C accelerated the LA production while also achieving the lowest energy consumption, which was 0.47 kWh/g LA at the highest LA production point. However, longer treatments at this temperature caused LA degradation. AlCl₃ has been identified as an ideal catalyst for biomass conversion to LA, being inexpensive and low in toxicity. Full article

The catalytic performance of copper in Fenton-like processes was investigated under conditions of elevated chloride concentrations. Model solutions were prepared containing four target pollutants (50 mg/L each), Cu (II) at 50 mg/L, and a stoichiometric dose of hydrogen peroxide sufficient for complete oxidation of the organic matter. Chloride levels ranged from low concentrations to those representative of both synthetic and natural seawater (36 g/L NaCl). An increase in chloride concentration consistently led to greater pollutant removal efficiency. The influence of pH on process performance was also assessed in saline and real seawater matrices. An optimal pH range between 6 and 7 was identified in both cases, where the reactivity of copper–chloride complexes was maximized while the formation of insoluble, catalytically inactive copper species was suppressed. Monitoring of pH, soluble copper concentration, and hydrogen peroxide consumption supported the conclusion that real seawater provides the most favorable conditions for copper–chloride catalyzed Fenton-like reactions. These results demonstrate the high potential of copper-based advanced oxidation processes in saline environments, particularly in applications where traditional methods exhibit limited efficiency. Full article

To address the disposal challenges of waste SCR catalysts and the urgent need for sustainable solutions in heavy metal pollution control, this study proposes a green resource utilization strategy based on the sub-molten salt method to convert waste SCR catalysts into highly efficient lead ion adsorbents. Titanate-based adsorbent materials with a loose porous structure were successfully prepared by optimizing the process parameters (reaction temperature of 160 °C, NaOH concentration of 70%, and reaction time of 2 h). The experiments showed that the adsorption efficiency was as high as 99.65% and the maximum adsorption capacity was 76.08 mg/g under ambient conditions (adsorbent dosage of 1.2 g/L, initial Pb(II) concentration of 100 mg/L, contact time of 60 min, and pH = 4). Kinetic analysis showed that the quasi-second-order kinetic model (R² = 0.9985) could better describe the adsorption process, indicating chemisorption as the dominant mechanism. Characterization analysis confirmed that subsequent to the adsorption process, Pb₃(CO₃)₂(OH)₂ formed on the surface of the adsorbent material is the adsorption product of Pb(II) and C-O through ion exchange and surface complexation. This study transforms waste SCR catalysts into sustainable titanate adsorbents through a low-energy green process, providing an eco-efficient solution for heavy metal wastewater treatment while aligning with circular economy principles and sustainable industrial practices. Full article

Fluoride-enriched geothermal groundwater poses chronic health risks (e.g., dental and skeletal fluorosis) through prolonged exposure; nevertheless, hydrochemical-driven factors and the genetic mechanism of fluoride enrichment in such systems remain inadequately identified. This study employed hydrochemical characterization, isotopic tracing, and health risk models to elucidate the genetic mechanism of fluoride-enriched geothermal groundwater. The key findings reveal the following. (1) Geothermal groundwater (Cl-Na type; TDS 90–345 mg/L; pH 6.25–7.42) contrasts with alkaline river water (pH 7.48–8.05; SO₄-Na/HCO₃-Na) and saline seawater (TDS 23.9–28.2 g/L). Stable isotopes (δD, δ¹⁸O) confirm atmospheric precipitation recharge with an elevation of 69–635 m. (2) The Self-Organizing Map algorithm categorized 30 geothermal samples into three groups: Cluster I—low temperature and pH, high TDS; Cluster II—high temperature, low F⁻ concentration; and Cluster III—low TDS, and high pH and F⁻ concentration. (3) Fluoride enrichment in Cluster III originated from the evaporite/fluorite dissolution under alkaline conditions and cation exchange interactions, while the inhibition of CaF₂ dissolution by reverse cation exchange limited the accumulation of F⁻ in Cluster II and Cluster III samples. (4) Health risks disproportionately affect children (80% high risk) and women, necessitating pre-use defluorination. Full article