Search Results (18,013)

The ion-adsorption-type rare earth element (iREE) deposits dominantly supply global resources of the heavy rare earth elements (HREEs), which have a critical role in a variety of advanced technological applications. The initial enrichment of REEs in the parent granites controls the formation of iREE deposits. Many Mesozoic and Cenozoic granites are associated with iREE mineralization in the Tengchong block, Southwest China. However, it is unclear how vital the mineralogical and geochemical characteristics of these granites are to the formation of iREE mineralization. We conducted geochronology, geochemistry, and Hf isotope analyses of the Yingpanshan–Damanbie granitoids associated with the iREE deposit in the Tengchong block with the aims to discuss their petrogenesis and illustrate the process of the initial REE enrichment in the granites. The results showed that the Yingpanshan–Damanbie pluton consists of syenogranite and monzogranite, containing REE-bearing accessory minerals such as monazite, xenotime, apatite, zircon, allanite, and titanite, with a high REE concentration (210–626 ppm, mean value is 402 ppm). The parent granites have Zr + Nb + Ce + Y (333–747 ppm) contents and a high FeO^T/MgO ratio (5.89–11.4), and are enriched in Th (mean value of 43.6 ppm), U (mean value of 4.57 ppm), Zr (mean value of 305 ppm), Hf (mean value of 7.94 ppm), Rb (mean value of 198 ppm), K (mean value of 48,902 ppm), and have depletions of Sr (mean value of 188 ppm), Ba (mean value of 699 ppm), P (mean value of 586 ppm), Ti (mean value of 2757 ppm). The granites plot in the A-type area in FeO^T/MgO vs. Zr + Nb + Ce + Y and Zr vs. 10,000 Ga/Al diagrams, suggesting that they are A₂-type granites. These granites are believed to have formed through the partial melting of amphibolites at a post-collisional extension setting when the Tethys Ocean closed. REE-bearing minerals (e.g., apatite, titanite, allanite, and fluorite) and rock-forming minerals (e.g., potassium feldspar, plagioclase, biotite, muscovite) supply rare earth elements in weathering regolith for the Yingpanshan–Damanbie iREE deposit. Full article

The limited supply of drinking water has aroused people’s curiosity in recent decades. Adsorption is a popular method for removing hazardous substances from wastewater, especially heavy metals, as it is cheap, highly efficient, and easy to use. In this work, a new sludge-based activated carbon adsorbent (thickened samples SBAC1 and un-thickened samples SBAC2) was developed to remove hazardous metals such as cadmium (Cd⁺²) and lead (Pb⁺²) from an aqueous solution. The chemical structure and surface morphology of the produced SBAC1 and SBAC2 were investigated using a range of analytical tools such as CHNS, BET, FT-IR, XRD, XRF, SEM, TEM, N₂ adsorption/desorption isothermal, and zeta potential. BET surface areas were examined and SBAC2 was found to have a larger BET surface area (498.386 m²/g) than SBAC1 (336.339 m²/g). While the average pore size was 10–100 nm for SBAC1 and 45–50 nm for SBAC2. SBAC1 and SBAC2 eliminated approximately 99.99% of Cd⁺² and Pb⁺² out the water under all conditions tested. The results of the adsorption of Cd⁺² and Pb⁺² were in good agreement with the pseudo-second-order equation (R² = 1.00). Under the experimental conditions, the Cd⁺² and Pb⁺² adsorption equilibrium data were effectively linked to the Langmuir and Freundlich equations for SBAC1 and SBAC2, respectively. The regeneration showed a high recyclability for the fabricated SBAC1 and SBAC2 during five consecutive reuse cycles. As a result, the produced SBAC1 and SBAC2 are attractive adsorbents for the elimination of heavy metals from various environmental and industrial wastewater samples. Full article

Tetracycline’s accumulation in the environment poses threats to human health and the ecological balance, necessitating efficient and rapid removal methods. Novel porous metal–organic framework (MOF) materials have garnered significant attention in academia due to their distinctive characteristics. This paper focuses on studying the adsorption and removal performance of amino-modified MIL-101(Fe) materials towards tetracycline, along with their adsorption mechanisms. The main research objectives and conclusions are as follows: (1) NH₂-MIL-101(Fe) MOF materials were successfully synthesized via the solvothermal method, confirmed through various characterization techniques including XRD, FT-IR, SEM, EDS, XPS, BET, and TGA. (2) NH₂-MIL-101(Fe) exhibited a 40% enhancement in tetracycline adsorption performance compared to MIL-101(Fe), primarily through chemical adsorption following pseudo-second-order kinetics. The adsorption process conformed well to Freundlich isotherm models, indicating multilayer and heterogeneous adsorption characteristics. Thermodynamic analysis revealed the adsorption process as a spontaneous endothermic reaction. (3) An increased adsorbent dosage and temperature correspondingly improved NH₂-MIL-101(Fe)’s adsorption efficiency, with optimal performance observed under neutral pH conditions. These findings provide new strategies for the effective removal of tetracycline from the environment, thus holding significant implications for environmental protection. Full article

The development of cost-effective and high-performance technologies for wastewater treatment is essential for achieving a sustainable economy. Among the various methods available for water remediation, adsorption is widely recognized as an effective and straightforward approach for removing a range of pollutants. Gel materials, particularly hydrogels and aerogels, have attracted significant research interest due to their unique properties. Hydrogels, for instance, are noted for their ability to be regenerated and reused, ease of separation and handling, and suitability for large-scale applications. Additionally, their low cost, high water absorption capacity, and contribution to environmental protection are important advantages. Aerogels, on the other hand, are distinguished by their low thermal conductivity, transparency, flexibility, high porosity, mechanical strength, light weight, large surface area, and ultralow dielectric constant. This review provides a comprehensive analysis of the current literature, highlighting gaps in knowledge regarding the classification, preparation, characterization, and key properties of these materials. The potential application of hydrogels and aerogels in water remediation, particularly in removing contaminants such as dyes, heavy metals, and various organic and inorganic pollutants, is also discussed. Full article

Pursuing improved electrode materials is essential for addressing the challenges associated with large-scale Li-ion battery applications. Specifically, silicon oxide (SiO_x) has emerged as a promising alternative to graphite anodes, despite issues related to volume expansion and rapid capacity degradation. In this study, we synthesized carbon-coated SiO_x using diatom biomass derived from artificially cultured diatoms. However, the inherent carbon content from diatoms poses a significant challenge for the electrochemical performance of diatom-based anodes in large-scale applications. Subsequently, we conducted further research and demonstrated excellent performance with a carbon content of 33 wt.% as anodes. Additionally, real-time characterization of the carbonization process was achieved using thermogravimetry coupled with infrared spectroscopy and gas chromatography mass spectrometry (TG-FTIR-GCMS), revealing the emission of CO and C₃O₂ during carbonization. Furthermore, electrochemical tests of the processed diatom and carbon (PD@C) anode exhibited outstanding rate capability (~500 mAh g⁻¹ at 2 A g⁻¹), high initial Coulomb efficiency (76.95%), and a D_Li⁺ diffusion rate of 1.03 × 10⁻¹² cm² s⁻¹. Moreover, structural characterization techniques such as HRTEM-SAED were employed, along with DFT calculations, to demonstrate that the lithium storage process involves not only reversible transport in Li₂Si₂O₅ and Li₂₂Si₅, but also physical adsorption between the PD and C layers. Exploring the integration of diatom frustules with the intrinsic carbon content in the fabrication of battery anodes may contribute to a deeper understanding of the mechanisms behind their successful application. Full article

Presently, ethylene oxide (EtO) is posing a significant threat to both human health and the environment due to occasional or deliberate emissions. However, few works so far have focused on this issue. It is urgent to explore novel and effective technology to protect against the threat of EtO. Herein, a series of AC/ZSM-5 composites were prepared to improve the adsorption performance for EtO, evaluated by dynamic breakthrough experiments. Particularly, the AC/ZSM-20% composite demonstrated a more excellent adsorption capacity of 81.9 mg/g at 25 °C and 50% RH than that of pristine AC and ZSM-5 with 32.5 and 52.3 mg/g, respectively. Moreover, the adsorption capacity of the AC/ZSM-20% composite remained constant even after five adsorption-desorption cycles. The adsorption mechanism of EtO on the composite is further revealed by density functional theory (DFT) calculations. Full article

Phenyl urea herbicides such as diuron and linuron are commonly used in agriculture to eliminate weeds. Their uncontrolled use can cause environmental problems. In this study, the adsorption of these herbicides was evaluated using activated carbon from coffee grounds, activated with zinc chloride (AC-ZnCl₂, 100% purity), nitric acid (AC-HNO₃, 65% purity), and commercially activated (AC-C) carbon for comparison purposes. The spent coffee grounds were transformed into activated carbon through the calcination process. The highest removal efficiency for diuron 40 mg∙L⁻¹ and linuron 31 mg∙L⁻¹ was obtained using the ZnCl₂-activated adsorbent, being 100% and 45%, respectively. The best pH range was between 4 and 6. Adsorption kinetic studies showed that pseudo-first and second-order models fit the experimental data, with the adsorption rate increasing rapidly within 60 min for the concentrations tested. Adsorption isotherms indicated that the Langmuir model provided the best fit for diuron, while the Freundlich model was more appropriate for linuron. The efficiency of the adsorption process using activated carbon (AC) was confirmed by the toxicity analysis of diuron and linuron solutions before and after adsorption with AC. Full article

The growing presence of diverse pollutants, including heavy metals, organic compounds, pharmaceuticals, and emerging contaminants, poses significant environmental and health risks. Traditional methods for pollutant removal often face limitations in efficiency, selectivity, and sustainability. This review provides a comprehensive analysis of recent advancements in innovative adsorbents designed to address these challenges. It explores a wide array of non-conventional adsorbent materials, such as nanocellulose, metal–organic frameworks (MOFs), graphene-based composites, and biochar, emphasizing their sources, structural characteristics, and unique adsorption mechanisms. The review discusses adsorption processes, including the basic principles, kinetics, isotherms, and the factors influencing adsorption efficiency. It highlights the superior performance of these materials in removing specific pollutants across various environmental settings. The practical applications of these adsorbents are further explored through case studies in industrial settings, pilot studies, and field trials, showcasing their real-world effectiveness. Additionally, the review critically examines the economic considerations, technical challenges, and environmental impacts associated with these adsorbents, offering a balanced perspective on their viability and sustainability. The conclusion emphasizes future research directions, focusing on the development of scalable production methods, enhanced material stability, and sustainable regeneration techniques. This comprehensive assessment underscores the transformative potential of innovative adsorbents in pollutant remediation and their critical role in advancing environmental protection. Full article

Background: Toluene exposure in construction workers can lead to several health problems, primarily affecting the nervous system, respiratory system, and skin. Utilizing advanced photocatalytic materials to degrade gaseous toluene aims to significantly mitigate its negative impact. Methods: In this research, photocatalysts based on pure TiO₂ and modified TiO₂ were synthesized to evaluate their efficacy in degrading gaseous toluene, a prevalent air pollutant in construction settings. Two synthesis methods were employed. Sonoprecipitation was used to create Fe-N co-doped TiO₂ nanoparticles in the first method, while the second method utilized co-precipitation and hydrothermal techniques without ultrasonic assistance to achieve Fe-N co-doping. Seven types of nanophotocatalysts were synthesized, including TiO₂-U (with ultrasonic assistance), NTiO₂-U, FeNTiO₂ (2.5)-U, FeNTiO₂ (5)-U, FeNTiO₂ (7.5)-U, FeNTiO₂ (10)-U, and FeNTiO₂ (5) without ultrasonic assistance. Characterization of the synthesized photocatalysts involved various analyses, including XRD, SEM, EDX, UV–VIS DRS, FT–IR, BET, and N₂ adsorption-desorption isotherm. Results: Ultrasonic assistance notably improved particle dispersion and prevented agglomeration on the photocatalyst surface. UV–VIS DRS analysis indicated a reduction in band gap energy due to Fe and N doping of TiO₂. The study also investigated the influence of Fe doping, initial toluene concentration, light source, and residence time on the degradation rate of gaseous toluene. Experimental findings showed that FeNTiO₂ (5)-U exhibited a higher degradation rate of toluene (63.5%) compared to FeNTiO₂ (5) (50%) under visible light irradiation over 15 s. Conclusions: The study underscores the significant enhancement in photocatalytic activity for toluene degradation achieved through the combined effects of ultrasound and co-doping methods. Full article

Herein, motivated by the excellent redox properties of rod-shaped ceria (CeO₂-NR), a series of TM/CeO₂ catalysts, employing the first-row 3d transition metals (Ti, V, Cr, Mn, Fe, Co, Ni, Cu, and Zn) as active metal phases, were comparatively assessed under identical synthesis and reaction conditions to decipher the role of active metal in the CO₂ hydrogenation process. Notably, a volcano-type dependence of CO₂ hydrogenation activity/selectivity was disclosed as a function of metal entity revealing a maximum for the Ni-based sample. Ni/CeO₂ is extremely active and fully selective to methane (Y_CH4 = 90.8% at 350 °C), followed by Co/CeO₂ (Y_CH4 = 45.2%), whereas the rest of the metals present an inferior performance. No straightforward relationship was disclosed between the CO₂ hydrogenation performance and the textural, structural, and redox properties, whereas, on the other hand, a volcano-shaped trend was established with the relative concentration of oxygen vacancies and partially reduced Ce³⁺ species. The observed trend is also perfectly aligned with the previously reported volcano-type dependence of atomic hydrogen adsorption energy and CO₂ activation as a function of 3d-orbital electron number, revealing the key role of intrinsic electronic features of each metal in conjunction to metal–support interactions. Full article

The main goal of this study is the examination of polypropylene (PP) microplastics (MPs) as possible carriers of daily use pharmaceutical compounds. The selected compounds can be separated into three groups: (i) antibiotics (Trimethoprim, Metronidazole, Indomethacin, Isoniazid), (ii) anti-inflammatories (Ketoprofen, Diclofenac), and (iii) anti-hypertensive (Valsartan). Two types of PP MPs (virgin and UV-aged) were used in the experimental procedure, and the effect of time and the effect of the initial concentrations of the drugs were examined. The impact of various environmental factors such as pH, salinity, and natural organic matter were also explored. The last two factors were studied using real aqueous matrices such as wastewater and seawater. According to the obtained results, the highest uptake was observed in indomethacin (9.3 mg/g) and diclofenac (7.3 mg/g), owing to their physiochemical properties. Aged particles showed enhanced adsorption ability in accordance with the existing literature, as their adsorption capacity was between 0.5–1.5 times greater than that of the virgin ones. Regarding the desorption of compounds from the virgin and aged PP MPs at three different pH values, diclofenac and indomethacin exhibited the highest desorption capacity, while alkaline conditions favored the desorption ability of PP MPs for most of the target compounds. Full article

This study evaluates the preparation of novel ternary functional adsorbents based on polyaniline, zinc oxide nanoparticles, and moringa oleifera gum to produce zinc oxide/Moringa oleifera gum-grafted L-methionine-functionalized polyaniline bionanocomposites (ZM-g-Pani) and employed to sequestrate divalent metal ions (Cd²⁺, Hg²⁺ and Pb²⁺) from wastewater samples. The morphological and structural properties of ZM-g-Pani were exploited using FT-IR, FE-SEM/EDS, TEM, and XRD. FT-IR and FE-SEM studies show that the as prepared nanocomposite has an abundant number of reactive groups and a porous structure, thus demonstrating outstanding divalent metal cation removal. FT-IR study confirms that the attachment of L-methionine to polyaniline is facilitated by the C-S linkage. Both TEM and FE-SEM techniques confirmed the clustered granules of ZnO over the surface of polyaniline, which ultimately provided more surface area to adsorb metal ions. The study demonstrated that Cd²⁺, Hg²⁺ and Pb²⁺ ions could undergo physical sorption and chemisorption simultaneously during the adsorption process. The maximum adsorption capacity was 840.33, 497.51, and 497.51 mg/g for Cd²⁺, Hg²⁺, and Pb²⁺, respectively. The impact of co-existing ions, including NO₃⁻, PO₄³⁻, SO₄²⁻, Cl⁻, Na⁺, Cu²⁺, and Al³⁺, showed that there were no notable alterations in the adsorption of the selected metal ions with ZM-g-Pani. ZM-g-Pani showed eight successive regeneration cycles for Cd²⁺, Hg²⁺, and Pb²⁺ with more than 85% removal efficiency. Full article

This study synthesized biochar through a one-pot pyrolysis process using IALG as the raw material. The physicochemical properties of the resulting biochar (IALG-BC) were characterized and compared with those of biochar derived from acid-treated lignin with the ash component removed (A-IALG-BC). This study further investigated the adsorption performances and mechanisms of these two lignin-based biochars for Pb(II). The results revealed that the high ash content in IALG, primarily composed of Na, acts as an effective catalyst during pyrolysis, reducing the activation energy and promoting the development of the pore structure in the resulting biochar (IALG-BC). Moreover, after pyrolysis, Na-related minerals transformed into particulate matter sized between 80 and 150 nm, which served as active adsorption sites for the efficient immobilization of Pb(II). Adsorption results demonstrated that IALG-BC exhibited a significantly superior adsorption performance for Pb(II) compared to that of A-IALG-BC. The theoretical maximum adsorption capacity of IALG-BC for Pb(II), derived from the Langmuir model, was determined to be 809.09 mg/g, approximately 40 times that of A-IALG-BC. Additionally, the adsorption equilibrium for Pb(II) with IALG-BC was reached within approximately 0.5 h, whereas A-IALG-BC required more than 2 h. These findings demonstrate that the presence of inorganic mineral components in IALG plays a crucial role in its resource utilization. Full article

A new class of biologics is obtained using the technologically processed of antibodies (TPA), which are used as the initial substance, and their dilution at each stage is accompanied by a controlled external vibrational (mechanical) treatment. This article focuses on the development and validation of a novel technique that can be applied for assessing the identity of TPA-based drugs. It has previously been found that after such treatment, the resulting solution either acquired new properties that were not present in the initial substance or a quantitative change in properties compared to the initial substance was observed. The use of mechanical treatment during the manufacture of the TPA-based drugs can cause the formation of new bonds between the solvent and antibody molecules. These changes manifest themselves in altered adsorption at the surface of the test solutions, which results in the formation of a near-surface film. One of the indicators of such events is the change in the surface temperature of the solution, which can be analyzed using high-resolution thermography. Unlike other methods, the high-resolution thermography allows the near-surface layer of a heterogeneous aqueous solution to be clearly visualized and quantified. A number of experiments were performed: seven replicates of sample preparations were tested; the influence of factors “day” or “operator” was investigated during 12 days of testing by two operators. The method also allowed us to distinguish between technologically processed antibodies and samples containing technologically processed buffer. The thermographic analysis has proven to be a simple, specific, and reproducible technique that can be used to analyze the identity of TPA-based drugs, regardless of the dosage form tested. Full article

Sewage sludge (SS) holds promise for environmental, agricultural, and energy applications. However, its direct use is limited due to contaminant concerns. Pyrolysis can turn SS into beneficial products like bio-oil and biochar. This study explores biochar production from SS pyrolysis and its potential for pollutant adsorption. The effects of pyrolysis temperature (500, 650, 850 °C) and SS particle size (800–1000 µm, 400–800 µm, 100–400 µm, ≤100 µm) on biochar yield and adsorption capacity for methylene blue and mercury were investigated. Regardless of particle size and temperature, SS-derived biochar exhibited second-order adsorption kinetics. Biochar with a particle size of 100–400 µm displayed the highest potential for methylene blue adsorption. Subsequent alkali treatment (biochar:NaOH = 3:4) of these particles significantly increased specific surface area from 27.5 m²/g to 144.27 m²/g and further enhanced adsorption capacities for both methylene blue (from 9 mg/g to 35 mg/g) and mercury (from 17 mg/g to 36 mg/g). These findings suggest that SS-derived biochar, particularly the 100–400 µm fraction with alkali treatment, presents a promising cost-effective adsorbent for water treatment, aligning with circular economy principles. Full article