Search Results (253)

Aimed at developing an economical and efficient biosorbent for the adsorption and separation of rare earth ions, this study employed Spirulina dry powder biomass as a biosorbent to investigate its removal performance for Pr³⁺ in aqueous solutions. Experimental results demonstrated that under optimized conditions (pH = 5, adsorbent dosage = 2.0 g/L, initial Pr³⁺ concentration = 100 mg/L, and adsorption time = 60 min), the removal efficiency of Pr³⁺ reached 79.0%. FT-IR and XPS characterization confirmed the participation of various functional groups on the Spirulina surface in the adsorption process. When 0.1 mol/L HNO₃ was used as the desorption agent, the desorption rate of Pr³⁺ from Spirulina reached 91.7%, demonstrating excellent regeneration performance. At different temperatures (298–318 K), the adsorption data were fitted using Langmuir, Freundlich, Dubinin–Radushkevich, and Redlich–Peterson models. Among them, the Langmuir model (R² ranged from 0.993 to 0.999) provided the best fit, and the adsorption capacity of Spirulina for Pr³⁺ was in the range of 51.10 to 55.31 mg/g. Kinetic studies revealed that the pseudo-second-order model (R² = 0.999) best described the adsorption process, with a rate constant of 0.054 g/(mg·min) (R² was 0.999) at an initial Pr³⁺ concentration of 300 mg/L, indicating chemisorption-controlled behavior. Thermodynamic parameter analysis showed that within the experimental temperature range, ΔG⁰ < 0 and ΔS⁰ > 0, confirming that the adsorption process was spontaneous and endothermic. This study provides a novel technical approach for the green recovery of rare earth elements and highlights the potential of Spirulina biomass in rare earth resource recycling. Full article

As a renewable alternative to fossil fuels, the industrial production of biodiesel urgently requires the development of efficient and recyclable solid base catalysts. In this study, the physicochemical properties and catalytic performance differences between MgO/Na₂CO₃ and MgO/K₂CO₃ catalysts were systematically compared using soybean oil as the raw material. By regulating the calcination temperature (500–700 °C), alcohol-to-oil ratio (3:1–24:1), and metal carbonate loading (10–50%), combined with N₂ adsorption–desorption, CO₂-TPD, XRD, SEM-EDS, and cycling experiments, the regulatory mechanisms of the ionic radius differences between sodium and potassium on the catalyst structure and performance were revealed. The results showed that MgO/Na₂CO₃-600 °C achieved a FAME yield of 97.5% under optimal conditions, which was 1.7% higher than MgO/K₂CO₃-600 °C (95.8%); this was attributed to its higher specific surface area (148.6 m²/g vs. 126.3 m²/g), homogeneous mesoporous structure, and strong basic site density. In addition, the cycle stability of MgO/K₂CO₃ was significantly lower, retaining only 65.2% of the yield after five cycles, while that of MgO/Na₂CO₃ was 88.2%. This stability difference stems from the disparity in their solubility in the reaction system. K₂CO₃ has a higher solubility in methanol (3.25 g/100 g at 60 °C compared to 1.15 g/100 g for Na₂CO₃), which is also reflected in the ion leaching rate (27.7% for K⁺ versus 18.9% for Na⁺). This study confirms that Na⁺ incorporation into the MgO lattice can optimize the distribution of active sites. Although K⁺ surface enrichment can enhance structural stability, the higher leaching rate leads to a rapid decline in catalyst activity, providing a theoretical basis for balancing catalyst activity and durability in sustainable biodiesel production. Full article

In this study, kaolinite-based clay (Ka-Clay) was used as an adsorbent for the efficient removal of Pb(II), Cd(II) and Hg(II) ions from aqueous media. The selection of Pb(II), Cd(II) and Hg(II) ions for experimental studies took into account their high toxicity, while the choice of Ka-Clay, the ease of preparation and high availability of this material were the most important arguments. Ka-Clay exhibits high adsorption performance, with removal percents over 98% for Pb(II) and 93% for Cd(II), even at high concentrations of metal ions (over 150 mg/L, pH = 6.5, 4 g adsorbent/L, 21 ± 1 °C). For Hg(II) ions, the adsorption percent does not exceed 55%, and this moderate value is mainly due to the significant change in pH. The adsorption behavior was in accordance with the Langmuir model (R² > 0.95) and the pseudo-second order kinetic model (R² > 0.99), indicating an adsorption process that occurs mainly through chemical interactions at the adsorbent surface between the metal ions and the functional groups. Adsorption processes are spontaneous (ΔG = −8.66 ÷ −15.76 kJ/mol) and endothermic (ΔH = 7.09 ÷ 21.81 kJ/mol), and the adsorption mechanism is the results of elementary processes of electrostatic attraction, ion exchange and superficial complexation. The insignificant effect of other ions (Ca(II), Mg(II), Na(I), K(I)) present in real wastewater samples as well as the desorption behavior of exhausted adsorbent highlight the practical utility of this adsorbent on a large scale. The experimental results included in this study suggest that Ka-Clay can be used as a promising adsorbent for the removal of high concentrations of toxic heavy metals with low cost and high efficiency, and this can contribute to the design of a sustainable wastewater treatment method. 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

In order to develop an efficient, environmentally friendly heavy metal ions adsorbent, the amino-modified expanded vermiculite-supported nano zero-valent iron (nZVI@PEI/EVMT) was prepared by using polyethyleneimine (PEI) as the functional reagent and expanded vermiculite (EVMT) as the carrier. The characterization results of nZVI@PEI/EVMT confirm that the PEI modification did not destroy the crystal configuration of EVMT, and when nano zero-valent iron (nZVI) was successfully loaded onto the PEI/EVMT surface, the value of saturation magnetic field was 41.5 emu/g, which could be separated from solution with magnet. The performance of Cr(VI) adsorption onto nZVI@PEI/EVMT was studied, showing that the ideal mass ratio for nZVI@PEI/EVMT was 1:1, and the removal capacity was largest when solution pH was 2. After four adsorption–desorption cycles, the adsorption amounts remained 40.1 mg/g. The Cr(VI) adsorption onto nZVI@PEI/EVMT was more consistent with a pseudo-second-order kinetics equation. Isotherm adsorption data accord with the Langmuir model, which suggests that the adsorption was the monolayer, the maximum adsorption amount was 116.2 mg/g at 30 °C and pH 2, and the adsorption was spontaneous and endothermic. It was inferred that the adsorption mechanisms included electrostatic attraction, reduction, chemical complexation, and co-precipitation. Full article

Antibiotic resistance has been recognized as a global threat to human health. Therefore, it is urgent to develop effective strategies to address the contamination of water environments caused by antibiotics. In this study, Fe/Mn bimetallic-modified biochar (FMBC) was synthesized through a one-pot oxidation/reduction-hydrothermal co-precipitation method, demonstrating an exceptional photocatalytic-Fenton degradation performance for oxytetracycline (OTC). Characterization techniques including FTIR, SEM, XRD, VSM, and N₂ adsorption–desorption analysis confirmed that the Fe/Mn bimetals were successfully loaded onto the surface of biochar in the form of Fe₃O₄ and MnFe₂O₄ mixed crystals and exhibited favorable paramagnetic properties that facilitate magnetic recovery. A key innovation is the utilization of biochar’s inherent phenol/quinone structures as reactive sites and electron transfer mediators, which synergistically interact with the loaded bimetallic oxides to significantly enhance the generation of highly reactive ·OH radicals, thereby boosting catalytic activity. Even after five recycling cycles, the material exhibited minimal changes in degradation efficiency and bimetallic crystal structure, indicating its notable stability and reusability. The photocatalytic degradation experiment conducted in a Fenton-like reaction system demonstrates that, under the conditions of pH 4.0, a H₂O₂ concentration of 5.16 mmol/L, a catalyst dosage of 0.20 g/L, and an OTC concentration of 100 mg/L, the optimal degradation efficiency of 98.3% can be achieved. Additionally, the pseudo-first-order kinetic rate constant was determined to be 4.88 min⁻¹. Furthermore, this study elucidated the detailed degradation mechanisms, pathways, and the influence of various ions, providing valuable theoretical insights and technical support for the degradation of antibiotics in real wastewater. Full article

The removal of Cr(VI) from wastewater is a crucial task due to its high toxicity. In this study, slumgum-originated biochar materials were obtained by three different methods: high-temperature pyrolysis with H₃PO₄ or CO₂ and the high-temperature treatment of CO₂-activated slumgum-originated biochar in an Ar atmosphere. The obtained materials were subjected to physicochemical characterization (nitrogen adsorption/desorption isotherms, CHN elemental analysis, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy) and tested for their adsorption properties towards Cr(VI) ions. The solution pH, contact time, and effects of the Cr(VI) concentration on Cr(VI) adsorption onto biochar materials were studied. The kinetics and isotherm experimental data were best fitted to the Elovich (R² = 0.848) and Freundlich (R² = 0.965) theoretical models for H₃PO₄-modified biochar. The highest adsorption capacity (45.0 mg g⁻¹) for Cr(VI) was obtained for biochar modified with H₃PO₄. It was stated that the relatively fast rate of Cr(VI) adsorption onto this biochar (equilibrium reached within 120 min) is related to its mesoporous structure. The mechanism of Cr(VI) adsorption onto H₃PO₄-modified biochar was studied in detail. The obtained biochar was successfully applied for efficient Cr(VI) removal from wastewater originating from spent bricks with a low biochar dosage (4.0 g L⁻¹). Full article

The rapid pace of industrialization has led to widespread heavy metal contamination in water and soil, highlighting the need for efficient remediation strategies. Among various approaches, adsorption has proven to be an effective method for treating contaminated environments. Layered double hydroxide (LDH) is frequently used in such applications. However, its adsorption efficiency remains limited. In this study, glutamic acid diacetate tetrasodium salt (GLDA) was incorporated into ZnAl LDH via a straightforward co-precipitation and ion exchange method, yielding a modified material, GLDA-LDH, which was subsequently applied for the adsorption of Pb(II) and Cd(II). Adsorption behavior was investigated through kinetic and isothermal models, with results indicating that the process followed pseudo-second-order kinetics and fit well with the Langmuir isotherm, suggesting chemisorption onto monolayer surface. The maximum adsorption capacities reached 219.2 mg/g for Pb(II) and 121.9 mg/g for Cd(II). Furthermore, GLDA-LDH exhibited a strong retention capability for metal ions with minimal desorption and remained effective in the presence of hard water and contaminated soils. XPS analysis revealed distinct interaction mechanisms; surface oxygen and carboxyl groups played a key role in Pb(II) adsorption, whereas nitrogen coordination was involved in Cd(II) uptake. These results point to the potential of GLDA-LDH as a reliable material for addressing heavy metal pollution and provide insights into the design of enhanced LDH-based adsorbents. Full article

The purification of waste cooking oils (WCOs) through clay-based adsorption is an established recycling method, yet the relationship between clay composition and adsorption efficiency remains an area of active research. The aim of the present research work was to assess the performance of Maghnia bentonite in WCO decoloration and to gain information about the specific refining process. Thus, natural bentonite from the Maghnia region (Algeria) was investigated as an adsorbent for WCO refining for biolubricant production. The adsorption efficiency was evaluated under different conditions, achieving up to 70% decolorization at 10 wt% clay after 4 h of treatment. Structural characterization of the bentonite before and after adsorption was conducted using FT-IR spectroscopy, powder X-ray diffraction (XRD), and X-ray fluorescence (XRF) to assess compositional and morphological changes. FT-IR analysis confirmed the adsorption of organic compounds, XRD indicated minor alterations in interlayer spacing, and XRF revealed ion exchange mechanisms, including a reduction in sodium and magnesium and an increase in calcium and potassium. Adsorption kinetics followed a pseudo-second-order model, with desorption effects observed at prolonged contact times. The pHPZC of 8.3 suggested that bentonite adsorption efficiency is enhanced under acidic conditions. The high decoloration capacity of Maghnia bentonite, combined with the availability and the low cost of the material, suggests a possible industrial application of this material for WCO refinement, especially in lubricant production. Full article

Graphene, being a two-dimensional monolayer of carbon, exhibits an exceptionally increased surface-to-volume ratio due to its atomic thinness and high aspect ratio, making it a material of considerable interest in advanced technology applications. Recent developments have leveraged their unique surface characteristics, such as nanoscale ripples and grooves, to enhance energy storage, sensing, catalysis, and environmental remediation performance. Its extensive surface area enables rapid ion adsorption and desorption, significantly improving energy and power densities in supercapacitors and lithium-ion batteries while enhancing stability over prolonged cycles. In sensing, the high surface-to-volume ratio supports the immobilization of biomolecules and nanoparticles, improving sensitivity in detecting gases, biomarkers, and pollutants, thereby advancing diagnostic and environmental monitoring applications. Its expansive surface area and unique electronic properties contribute to high catalytic efficiencies, enabling sustainable chemical processes, such as hydrogen production, water treatment, and pollutant degradation. Unlike many review articles that primarily explore the functionalization of graphene, this study mainly emphasizes the evaluation of methodologies aimed at augmenting graphene’s surface area. This review systematically evaluates recent advancements in the optimization of graphene surface characteristics, with a primary focus on their role in enhancing energy storage systems while also addressing emerging applications in healthcare and environmental sustainability. Full article

Rice husk (RH), a globally abundant agri-food waste, presents a promising renewable silicon source for producing SBA-15 mesoporous silica-based materials. This study aimed to synthesize and bifunctionalize SBA-15 using RH as a silica precursor, incorporating sulfonic and octadecyl groups to create a mixed-mode sorbent, RH-SBA-15-SO₃H-C18, with reversed-phase and cation exchange properties. The material’s structure and properties were characterized using advanced techniques, including X-ray diffraction, infrared spectroscopy, N₂ adsorption–desorption isotherms, nuclear magnetic resonance, and electron microscopy. These analyses confirmed an ordered mesoporous structure with a high specific surface area of 238 m²/g, pore volume of 0.45 cm³/g, pore diameter of 32 Å, and uniform pore distribution, highlighting its exceptional textural qualities. This sorbent was effectively utilized in solid-phase extraction to purify 29 alkaloids from three families—tropane, pyrrolizidine, and opium—followed by an analysis using ultra-high performance liquid chromatography coupled to ion-trap tandem mass spectrometry. The developed analytical method was validated and applied to gluten-free bread samples, revealing tropane and opium alkaloids, some at concentrations exceeding regulatory limits. These findings demonstrate that RH-derived RH-SBA-15-SO₃H-C18 is a viable, efficient alternative to commercial sorbents for monitoring natural toxins in food, offering a sustainable solution for repurposing agri-food waste while addressing food safety challenges. Full article

The adsorption capacity of a biochar (BC) obtained from pine wood residues was evaluated for its ability to remove two pharmaceuticals: fluoxetine (FLX) and sulfamethizole (SMZ). The material showed promising results in FLX removal, but a limited capacity in the case of SMZ. In order to improve these results, BC surface modifications were made by doping with nitrogen, as well as using acid, basic and electrochemical treatments. A three-dimensional electrosorption treatment proved to be the most effective, increasing the adsorption rate from 0.45 to 13.46 mg/g after evaluating different operating conditions, such as the electrodes used or the BC dosage. Consecutive cycles of BC use were performed through desorption and electro-regeneration techniques to test its capacity for reuse, and it was observed that application in the 25 mA electric field increased the useful life of the material. Finally, the effect of ionic strength was studied, highlighting that the presence of ions did not significantly affect the efficiency of SMZ removal, although a slight increase was observed at a high ion concentration, probably due to a salinization effect. Full article

The removal of cadmium ions (Cd²⁺) using raw argan shells (ArS) was optimized through experimental and theoretical studies. Adsorption experiments revealed optimal conditions at an adsorbent dose of 3.5 g, an initial Cd²⁺ concentration of 20 mg·L⁻¹, and a pH of 8, achieving a maximum sorption capacity of 3.92 mg·g⁻¹. The kinetic analysis showed that the adsorption followed a pseudo-second-order model (R² = 0.98), and the Langmuir isotherm model predicted a maximum adsorption capacity of 4 mg·g⁻¹. Thermodynamic analysis indicated an endothermic adsorption process, with ΔG° shifting from positive to negative as temperature increased, confirming that adsorption is favored at higher temperatures. Desorption studies demonstrated that HCl was the most effective eluting agent, achieving a desorption efficiency of 90.02%, followed by HNO₃ (76.65%) and CH₃COOH (71.59%). The varying desorption efficiencies were attributed to differences in acid strength and ionic interactions with Cd²⁺. This study demonstrates the potential of raw argan shells as an efficient, reusable, and sustainable biosorbent for cadmium removal, offering a promising solution for water treatment and environmental remediation. Full article

The reduction of unfriendly 4-nitrophenol to make it unimpactful with the environment (4-aminophenol) was carried out using the metastable form of copper ferrite (CuFe₅O₈) synthesized by the co-precipitation of metal nitrate salts, an efficient method with inexpensive and abundant starting materials. The samples were obtained by calcination at various temperatures ranging from 600 °C to 900 °C. The material characterizations, including X-ray diffraction, N₂ adsorption/desorption, scanning electron microscope, X-ray absorption spectroscopy, and ultraviolet–visible spectrometry, were employed to identify the detailed structures and describe their correlations with catalytic activities. The X-ray diffraction and X-ray absorption spectroscopy analyses revealed the presence of mixed CuFe₅O₈ and copper oxide phases, where the formers are rich in Cu²⁺, Fe²⁺, and Fe³⁺ ions. The electron transfer between Cu²⁺, Fe²⁺, and Fe³⁺ led to the high efficiency of the catalytic reaction of the synthesized copper ferrites. Especially for the sample calcined at 600 °C, the apparent kinetic constant (k) for a reduction of 4-nitrophenol was equal to 0.25 min⁻¹, illustrating nearly 100% conversion of 4-nitrophenol to 4-aminophenol within less than 9 min. Regarding the N₂ adsorption/desorption isotherms, the samples calcined at 600 °C have the highest specific Brunauer–Emmett–Teller (BET) surface area (15.93 m² g⁻¹) among the others in the series, which may imply the most effective catalytic performance investigated herein. The post-catalytic X-ray diffraction investigation indicated the stability of the prepared catalysts. Furthermore, the chemical stability of the prepared catalysts was confirmed by its reusability in five consecutive cycles. Full article

Thiophenol (synonyms: phenyl mercaptan, benzenethiol) may appear in the aquatic environment as a result of human activity. It is used as a raw material in organic synthesis in various industries for the production of dyes, pesticides, pharmaceuticals and polymers, such as polyphenylene sulfide (PPS). It may also enter water through contamination with petroleum substances (thiophenol may be present in crude oil). Due to the fact that thiophenol is toxic to living organisms, its removal from water can be a very important task. For the first time, this paper presents experimental studies of the sorption and desorption process of thiophenol on an ion exchange resin. Thiophenol sorption experiments on AmbeLite^®IRA402 (Cl form) were tested at different pH levels (4, 7, and 9) and different ionic strengths of the aqueous solution. Its detection in water was carried out using UV spectroscopy. At pH 4, the thiophenol sorption process is basically independent of the ionic strength of the solution, but also the least effective. The sorption capacity of a thiophenol solution in distilled water is about 0.37–0.46 mg/g, for a solution with an ionic strength of 0.1 M 0.42 mg/g. At pH 7 and 9, the sorption of thiophenol from an aqueous solution is similar and definitely more effective. The sorption capacity of the thiophenol solution in distilled water is about 13.83–14.67 mg/g, and for a solution with an ionic strength of 0.1 M, it is 2.83–2.10 mg/g. The desorption efficiency of thiophenol from AmbeLite^®IRA402 resin (washing with 4% HCl) at pH 7 is 90%, which is promising for the resin reuse process. Kinetic studies were performed and a pseudo-first-order and second-order kinetic model was fitted to the obtained experimental sorption data. In most cases, the simulation showed that the pseudo-second-order model gives a better fit, especially for the sorption of thiophenol from the solution with an ionic strength of 0.1 M. The fit of the Freundlich and Langmuir isotherm models to the experimental results indicates that the latter model provides better agreement. Analysis of the infrared spectra supported by quantum chemical calculations (DFT/PCM/B3LYP/6-31g**) confirms the experimental results observed during the sorption process. At pH 7 and 9, the thiophenol is sorbed in anionic form and—together with the ion exchange processes that occur between the dissociated thiol group and the quaternary ammonium group—an interaction between the aromatic structures of thiophenolate anions and IRA402 also takes place. Full article