Search Results (9)

The elimination of toxic and long-lasting dyes like crystal violet (CV) from wastewater continues to be a major environmental challenge. Considering this, in this study, a novel amine-modified adsorbent was synthesized by functionalizing ZIF-67 with phosphorylethanolamine (PEA@ZIF-67) nanocomposite to enhance dye removal efficiency. Comprehensive characterization of PEA@ZIF-67 nanocomposite using FTIR, XRD, TGA, and BET techniques confirmed the successful incorporation of PEA into ZIF-67 without compromising the structural integrity of the ZIF-67. The BET specific surface area of PEA@ZIF-67 nanocomposite was noted to be 145.3 m²/g. Furthermore, the application of PEA@ZIF-67 nanocomposite for CV adsorption was investigated and optimized using the Response Surface Methodology (RSM) technique, with the adsorbent dosage, initial dye concentration, and temperature as the operational variables. Under optimized conditions, q_max was 4348 mg/g. Adsorption kinetic studies showed the Avrami model to best fit the respective CV adsorption results, suggesting a heterogeneous and time-dependent mechanism. On the other hand, the Redlich–Peterson adsorption isotherm, which signifies a hybrid adsorption behavior, was noted to be effective. The thermodynamic studies confirmed that the CV adsorption onto PEA@ZIF-67 is spontaneous, endothermic, and entropy-driven. The post-adsorption FTIR and XRD analyses indicated that the used PEA@ZIF-67 was stable, thus supporting its reuse capability. Full article

Macroinvertebrates are a crucial part of aquatic ecosystems and significantly contribute to the maintenance of their health and stability. Our aims were to explore spatio-temporal patterns in macroinvertebrate communities and evaluate the ecological health of various parts of the Poyang Lake Basin during the early stage of a fishing ban. We collected samples using a Peterson grab sampler and conducted ecological evaluations using the B-IBI index. A total of 107 species of macroinvertebrates were identified, and most species were arthropods. The density and biomass of macroinvertebrates significantly differed among seasons and water bodies. No significant differences in diversity among seasons were observed; however, diversity significantly varied among water bodies. Environmental parameters such as water depth, pH, turbidity, total nitrogen, total phosphorus, and chlorophyll a played a crucial role in shaping the community structure of macroinvertebrates. Most of the sampling sites were classified as healthy or sub-healthy, indicating that the fishing ban policy has started to have a positive effect. The effects of this ban are achieved through a cascading sequence of processes, including the elimination of fishing disturbance, the restoration of habitat structure, and the reallocation of trophic energy, in addition to increases in microhabitat diversity associated with habitat heterogeneity. Together, these processes drive the multidimensional recovery of macroinvertebrate communities, manifested as increased species richness, higher density and biomass, and elevated B-IBI scores. Full article

To address challenges in locating high-impedance grounding faults (HIGFs) and isolating fault areas in resonant grounding systems, this paper proposes a novel fault identification method based on coordinating a Peterson coil and a resistance grounding system. This method ensures power supply reliability by extinguishing the fault arc during transient faults with the Peterson coil. When a fault is determined to be permanent, the neutral point switches to a resistance grounding mode, ensuring regular distribution of zero-sequence currents in the network, thereby addressing the challenges of HIGF localization and fault area isolation. Fault calibration and nature determination rely on recognizing neutral point displacement voltage waveforms and dynamic characteristics, eliminating interference from asymmetric phase voltage variations. Fault area identification involves assessing the polarity of zero-sequence current waveforms attenuation during grounding mode switching, preventing misjudgments in grounding protection due to random initial fault angles and Peterson coil compensation states. Field experiments validate the feasibility of this fault location method and its control strategy. Full article

The employment of compounds obtained from natural sources to produce adsorbents and their application in the elimination of antibiotics from industrial effluents have gained significant attention because of their low production cost and sustainability. Herein, chitosan (biopolymer) and smectite (abundant clay mineral) were used for the low-cost and eco-friendly synthesis of a new type of adsorbent. A low-energy-consumption hydrothermal process was applied to the synthesis of the chitosan-derived carbon–smectite nanocomposite with cobalt (H_Co/C-S). The produced nanocomposite was characterized using elemental analysis, ICP-OES, XRPD, low-temperature N₂ adsorption–desorption isotherms, FTIR analysis, and point of zero charge. H_Co/C-S (S_BET = 0.73 m² g⁻¹, d₀₀₁ = 1.40 nm, pH_PZC = 5.3) was evaluated as a ciprofloxacin adsorbent in aqueous solution. Experimental data were fitted with different kinetic models and interpreted by selected adsorption isotherms. The pseudo-second-order model was found to be the most appropriate, while ciprofloxacin adsorption onto H_Co/C-S was best described by the Redlich–Peterson isotherm (R² = 0.985). The maximum adsorption capacity of H_Co/C-S, according to the Langmuir isotherm (R² = 0.977), was 72.3 mg g⁻¹. Desorption and thermodynamic studies were performed. The obtained results indicated that the new hierarchically designed H_Co/C-S has promising potential to be further tested for application in real wastewater treatment. Full article

Hexavalent chromium [Cr (VI)] is a highly toxic and hazardous contaminant that poses serious health risks to both humans and the environment. Its presence in water sources can lead to severe health issues, including various types of cancer and respiratory ailments. Therefore, developing efficient and effective methods for Cr (VI) removal is crucial in ensuring safe and clean water supplies. The aim of this research is the environmentally responsible elimination of hexavalent chromium by bioadsorption using corn residues (CR), palm fiber (PF), and the peels of yam (YP), cassava (CP), and cocoa (CH). The study was conducted with varying levels of pH, bioadsorbent quantity, temperature, and adsorbent particle size at 200 rpm, with an initial concentration of 100 mg/L and 24 h of contact time to improve the adsorption efficiency. The process variables were evaluated and optimized using the statistical technique response surface methodology (RSM). The SEM-EDS analysis revealed that the predominant elements in the structure of the bioadsorbents were carbon and oxygen. Furthermore, the adsorption process led to the incorporation of Cr (VI) into the structure of the biomaterials, as indicated by their EDS spectra. The maximal adsorption efficiency of 99.11% was obtained at pH 2, bioadsorbent dose of 0.03 mg, 30 °C, and 0.5 mm of particle size. Various equilibrium isotherms were utilized to fit and analyze the adsorption data. The assessed maximum adsorption capacities were 38.84, 56.88, 52.82, 138.94, and 240,948.7 mg/g for YP, PF, CP, CH, and CR, respectively. The adsorption data exhibited conformity with the Freundlich and Redlich–Peterson isotherm models (R² = 0.95), indicating that the phenomenon occurs in a multilayer. Pseudo-second order and Elovich kinetic models adjusted the kinetics of chromium (VI), suggesting that the mechanism could be controlled by chemisorption. Therefore, the residual biomasses evaluated can serve as a cost-effective adsorbent for Cr (VI) removal, and the use of RSM enables efficient modeling and prediction of the adsorption process. Full article

In the current study, polyaniline and polypyrrole with silicon dioxide (PAni:PPy@SiO₂) were combined to formulate a new adsorbent, which was examined using XRD, TEM, SEM, FTIR, TGA, and BET, and the adsorption kinetics were investigated by UV–vis spectroscopy. The optical band gap was also evaluated. The electrochemical behavior was investigated using cyclic voltammograms. Moreover, experimental conditions were used to evaluate the 2,4-dichlorophenol (2,4-DCP) adsorption based on the pH, temperature, reaction time, and initial concentration. The analytical isotherm data were determined by Langmuir, Freundlich, Temkin, Sips, and Redlich–Peterson models. For the analysis of the kinetic data, the pseudo-first- and -second-order models and the intraparticle diffusion model were investigated. It was found that this new adsorbent possessed the highest adsorption efficiency after several regeneration cycles. Furthermore, the thermodynamic parameters of adsorption, such as entropy (ΔS), enthalpy (ΔH), and standard Gibbs were measured. These results suggest that the PAni:PPy backbone can generally be better applied for the elimination of 2,4-dichlorophenol by appropriately dispersing it over the surface of suitable SiO₂. This search provides a novel way to develop separable, high-performance adsorbents for adsorbing organic contamination from wastewater. Full article

A convenient regioselective synthesis of allyl- and vinylsilyl alcohols, from a common precursor, was described, by selecting the appropriate reaction conditions. Allyl- and vinylsilyl alcohols were tested in silyl-Prins cyclizations for the preparation of disubstituted oxygenated heterocycles in a one-pot sequential reaction. The methodology was sensitive to the structure of the starting alkenylsilyl alcohol and reaction conditions, with competitive pathways observed (particularly for allylsilyl alcohols), such as Peterson elimination and oxonia-Cope reactions. However, the use of vinylsilyl alcohols allowed the preparation of differently disubstituted cis-2,6-dihydropyrans in moderate to good yields. Computational studies support the proposed mechanism. Full article

In this study, a low-cost granular activated carbon doped with Fe₂O₃ nanoparticles (Fe–GAC) was prepared via a modified sol-gel technique and utilized for the elimination of lead (Pb(II)) and chromium (Cr(T)) ions from synthetic and actual brackish water. The effect of adsorption parameters on the removal of Pb(II) and Cr(T) ions from the water was evaluated in batch adsorption tests. The characterization results validated the distribution of well-defined Fe₂O₃ nanoparticles onto the GAC surface. GAC loaded with 5 wt.% of Fe₂O₃ (Fe–GAC 5) exhibited a maximum surface area of 848.2 m² g⁻¹. The equilibrium data of Cr(T) adsorption were in close agreement with the Langmuir and Sips models with R² values of 0.95 and 0.96, respectively. However, the R² values of the equilibrium data for Pb(II) adsorption were greater than 0.91 for all four models, i.e., Langmuir, and Sips, Freundlich and Redlich-Peterson. The maximum Langmuir adsorption capacities of Pb(II) and Cr(T) by Fe–GAC 5 at pH 5.6 and room temperature were 11.9 and 22.1 mg g⁻¹, respectively. Pseudo-second order (R²_Pb(II) = 0.99, R²_Cr(T) = 0.99) and Elovich kinetic models (R²_Pb(II) = 1, R²_Cr(T) = 1) were found the most suitable for describing the adsorption kinetics data of Pb(II) and Cr(T) using Fe–GAC 5. The adsorption/desorption studies illustrated that the Fe–GAC is reusable and can be regenerated using 1.0 M HCl. Moreover, the Fe–GAC 5 was found effective to reduce heavy metals loading in actual brackish water to the allowed international standards of drinking water. Accordingly, the Fe–GAC could be a promising material for large-scale applications for the elimination of heavy metals from water. Full article

Starting from 2-(triphenylsilyl)ethanol a new oxycarbonyl protecting group cleavable by fluoride ion induced Peterson-elimination has been developed. Known 2-(triphenylsilyl)ethanol has been prepared from commercially available triphenylvinyl-silane by a hydroboration-oxidation sequence using the sterically hindered borane reagent 9-BBN. The silyl alcohol was subsequently transformed into its chloroformate, imidazolylcarboxylic acid ester and p-nitrophenyl carbonate and used in standard protocols for the formation of carbamates and carbonates. The Tpseoc group proved to be highly resistant against acidic conditions applied in removal of tert-butyl esters and the t-Boc-group. It also withstood catalytic hydrogenation, treatment with morpholine, methylhydrazine and Pd-reagents/allyl-scavanger combinations, conditions required to cleave Cbz-, Fmoc-, phthalimide- and Alloc-groups. The Tpseoc-group is cleaved upon treatment with TBAF/CsF at 0 °C or r.t. with cleavage times reaching from < 10 min. to 24 h. Its orthogonality, ease of cleavage and UV-detectability makes the Tpseoc-group a promising alternative to other widely used silicon based amine protecting groups like the Teoc- and SES-groups. Full article