Search Results (5,249)

Tetracycline has been widely used as an efficient broad-spectrum antibiotic, while its long-term environmental pollution characteristics have gradually gained recognition and attention, highlighting the urgent need to identify a low-cost and effective method for removing tetracycline pollutants. This study aims to develop a one-step bamboo-based biochar preparation method based on a KCl-ZnCl₂ molten salt system; the potential application of obtained bamboo-based biochar as a tetracycline adsorbent was characterized and analyzed. Results show that the biochar prepared at 900 °C possesses abundant microporous and mesoporous structures, with abundant surface functional groups. Also, it exhibits a composite type I/IV isotherm, with a specific surface area of 1305.91 m²·g⁻¹, a total pore volume of 0.944 cm³·g⁻¹, demonstrating excellent tetracycline adsorption capacity of 298.93 mg·g⁻¹. XRD analysis confirmed that increasing the activation temperature significantly enhanced the graphitization degree of the biochar, which is a key factor influencing its tetracycline adsorption performance. Kinetic studies indicated that the adsorption kinetic process was better described by the Elovich model and Freundlich isotherm. Furthermore, cost-effectiveness analysis revealed that the cyclic preparation cost of biochar via this technique could be reduced to 18.25 USD per kilogram owing to the low consumption characteristics of the KCl-ZnCl₂ molten salt, which represents a 93.4% reduction compared with conventional preparation methods, underscoring the economic applicability of this technology in the field of tetracycline removal. The findings of this study are expected to lay a foundation for the industrial preparation of low-cost, high-performance bamboo-based biochar for tetracycline removal. Full article

Conventional casting of 5N5 high-purity aluminum often results in coarse grains, microstructural inhomogeneity, and a low equiaxed grain area fraction. Vacuum casting in a graphite mold was integrated with multidirectional mechanical vibration to refine and homogenize the solidification microstructure. A three-factor, three-level Box–Behnken design combined with response surface methodology was employed to optimize pouring temperature (A), mold temperature (B), and vibration frequency (C), with the average grain size (Y₁) minimized and the average shape factor (Y₂) and equiaxed grain area fraction (Y₃) maximized. Analysis of variance indicated statistically significant quadratic models with a non-significant lack of fit. The predicted optimum (A ≈ 714 °C, B ≈ 363 °C, C ≈ 37 Hz) was validated experimentally, producing a refined and highly equiaxed structure (Y₁ ≈ 0.85 ± 0.02 mm, Y₂ ≈ 0.84 ± 0.04, Y₃ ≈ 88.6 ± 2.11%), consistent with model predictions. Multidirectional vibration strengthens melt convection and interfacial shear, which is considered to promote grain multiplication and increase the number of effective nuclei, thereby accelerating the columnar-to-equiaxed transition and improving microstructural uniformity. Full article

Single-crystal 4H-SiC, as a wide-bandgap semiconductor material, has become a key substrate for high-power electronics and radio frequency devices due to its outstanding characteristics such as high-voltage tolerance, high-temperature stability, high-frequency efficiency and low loss. However, its inherent properties of high hardness and low fracture toughness also pose severe challenges to the ultra-precision processing of wafer substrates. In this study, through molecular dynamics methods, the influence of diamond abrasive grains with different sharpness on the processing of 4H-SiC at different grinding speeds was simulated, with a focus on analyzing its surface morphology, material removal behavior and subsurface damage characteristics. The structural evolution of 4H-SiC workpieces and diamond abrasive grains was identified through the radial distribution function, and the dynamic changes in temperature and stress during processing were further investigated to clarify the mechanism of abrasive wear and graphitization phenomena. The results show that regular octahedral abrasive grains with higher sharpness have better material removal efficiency, but they also cause more significant subsurface damage. Increasing the grinding speed helps to reduce the depth of subsurface damage. In addition, high temperature and high stress are the key factors leading to the transformation of diamond into graphite. Even under low-speed grinding conditions, the edges of the abrasive grains may still undergo graphitization due to stress concentration. The above findings have theoretical significance for an in-depth understanding of the material removal mechanism of 4H-SiC nano-grinding, and can also provide an important reference for the development of high-performance grinding wheels for SiC grinding. Full article

Epoxy resins (EP) are widely used in aerospace, electronics, and coatings due to their excellent mechanical and thermal properties. However, their inherent flammability and brittleness limit high-end applications. In this work, a novel reactive flame retardant epoxy monomer (EP-DVGA) containing DOPO and triazole units was designed and synthesized via a molecular engineering strategy. The chemical structure was confirmed by FTIR and NMR. A series of modified epoxy thermosets were prepared by co-curing EP-DVGA with bisphenol A epoxy resin (E51) using DDM as curing agent. The results showed that EP-DVGA significantly enhanced flame retardancy: At 16.31 wt% loading, the limiting oxygen index increased from 25.9% to 34.3% with UL-94 V-0 rating, and cone calorimetry revealed 73.2% and 69.2% reductions in peak heat release rate and total heat release, respectively. Mechanistic studies demonstrated a dual flame retardant effect involving phosphorus radical quenching in the gas phase and formation of a dense graphitized char layer in the condensed phase. Remarkably, EP-DVGA also improved mechanical properties—impact strength increased by 47% and tensile strength by 33.1% at optimal loadings—attributed to energy dissipation through reversible hydrogen bonding and π–π interactions. This molecular design successfully overcomes the traditional trade-off between flame retardancy and mechanical performance, offering a promising strategy for developing high-performance intrinsically flame retardant epoxy materials. Full article

To overcome the inherent limitations of graphitic carbon nitride (g-C₃N₄), specifically the rapid recombination of photogenerated electron–hole pairs and its confined light absorption range, a sulfur-doped g-C₃N₄ (S-g-C₃N₄) photocatalyst was developed in this work. The photocatalytic performance and its catalytic mechanism for rhodamine B (RhB) degradation were systematically investigated. Material characterization and performance tests revealed that S doping can narrow the band gap of g-C₃N₄ and effectively enhance the separation and transport efficiency of charge carriers. The as-prepared catalyst demonstrated excellent activity under simulated sunlight, achieving nearly complete degradation of 10 mg/L RhB within 15 min. Moreover, it exhibited robust stability across a pH range of 6 to 11 and in the presence of coexisting anions (Cl⁻, NO₃⁻, CO₃²⁻), with negligible activity loss after five consecutive cycles. Radical trapping experiments verified that ∙OH radicals served as the primary active species, with h⁺ playing a secondary role in the degradation process. This work provides practical guidance for designing durable g-C₃N₄-based photocatalysts with high performance for organic wastewater treatment. Full article

To address critical challenges in marine oil spill remediation, including limited penetration of high-viscosity crude oil and inefficient adsorbent recovery, it is imperative to develop environmentally friendly materials integrating high-efficiency adsorption, in situ viscosity reduction, and controllable recovery. In this study, a delignified corn pith (CPDL) with a three-dimensional porous structure was employed as a green matrix. Through constructing a Fe₃O₄/expansible graphite (EG)/polyvinylidene fluoride (PVDF) composite functional coating combined with silanization modification, a multifunctional biomass-based oil sorbent (Fe₃O₄/EG/PVDF-CPDL) was successfully fabricated. The material maintains the inherent porous architecture while forming a stable micro/nano-rough surface, exhibiting excellent superhydrophobicity with a water contact angle of approximately 155°, and demonstrating exceptional stability in harsh acidic/alkaline/saline environments and multiple cycles. Benefiting from the synergistic photothermal effect of Fe₃O₄ and EG, under one sun illumination (1 kW/m²), the material surface temperature rapidly reaches above 80 °C within 100 s, reducing the viscosity of high-viscosity crude oil by over 95% (from 1.39 × 10⁵ to approximately 6.0 × 10³ mPa·s), thereby enabling rapid penetration and adsorption within 50 s. Moreover, the composite coating significantly enhances mechanical performance, achieving a compressive strength of 320 kPa (approximately eight times higher than that of the pristine substrate), ensuring structural integrity during handling and compression recovery. Meanwhile, the material demonstrates precise directional manipulation and efficient recovery through external magnetic fields due to its superior magnetic responsivity. Experimental results reveal a broad-spectrum adsorption capacity (14.8–30.2 g/g) and separation efficiency exceeding 96% after 20 adsorption–desorption cycles. In summary, this work presents an innovative strategy with significant application potential for efficient and controllable remediation of marine oil spills, particularly high-viscosity crude oil, by integrating synergistic functions of porous adsorption, superhydrophobic corrosion resistance, photothermal viscosity reduction, mechanical reinforcement, and magnetic control. Full article

Photocatalytic H₂O₂ synthesis emerges as a promising green substitute for the energy-intensive anthraquinone process, yet its efficiency is limited by rapid charge recombination and limited surface active sites in bulk polymeric semiconductors. Herein, we report a topology-directed strategy to tailor the interlayer interactions of graphitic carbon nitride (g-C₃N₄), yielding ultrathin nanosheets with optimized electronic structures. The resulting catalyst exhibits an exceptional H₂O₂ production rate of 1.34 mmol g⁻¹ h⁻¹ under visible light, surpassing bulk g-C₃N₄ by a factor of 2.48. Water contact angle measurements confirm the superior hydrophilicity of the engineered nanosheets, facilitating interfacial mass transfer, while in situ FTIR and EPR spectroscopies unravel that the abundant exposed active sites optimize the adsorption configuration of the key *OOH intermediate and promote the generation of •O₂⁻ and •OH radicals. Regarding charge transfer dynamics, in situ EPR trapping experiments and Kelvin probe force microscopy (KPFM) reveal that the attenuated interlayer coupling induces a robust internal electric field, effectively suppressing carrier recombination and prolonging the exciton lifetime by a factor of 1.249. This work establishes a quantitative structure–activity relationship between interlayer engineering and exciton dynamics, offering a reliable protocol for the rational design of high-performance molecular photocatalysts. Full article

Efficient charge transfer and effective separation of photo-generated charge carriers are pivotal to the photocatalytic process. In this study, a novel CoAl₂O₄@nitrogen-doped graphitic carbon (CoAl₂O₄@NGC) composite photocatalyst was fabricated via a stepwise hydrothermal method coupled with high-temperature calcination, and its photocatalytic performance for CO₂ reduction was systematically investigated. X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and photoelectrochemical measurements were employed to characterize the phase structure, microstructure, surface chemical state and photoelectrochemical properties of the catalyst. Spinel-structured CoAl₂O₄ nanoparticles were uniformly anchored on the NGC substrate, forming a well-integrated composite interface. XPS analysis confirmed the coexistence of Co²⁺/Co³⁺ mixed valence states in CoAl₂O₄ which provides abundant redox sites for CO₂ activation. Photocatalytic tests showed that CoAl₂O₄@NGC exhibits excellent catalytic activity and cycling stability, with CO and CH₄ yields of 27.88 μmol·g⁻¹·h⁻¹ and 23.90 μmol·g⁻¹·h⁻¹, respectively. The narrow bandgap (1.54 eV) enhances visible light absorption, while efficient electron-hole separation and reduced charge transfer resistance improve photocatalytic efficiency. Theoretical calculations further reveal that CoAl₂O₄@NGC lowers the adsorption free energy of CO₂ and the energy barrier for COOH formation, thus facilitating the photocatalytic CO₂ reduction. This work provides insights for the design of efficient and stable photocatalysts for CO₂ reduction and deepens the understanding of the synergistic catalytic mechanism in the spinel/nitrogen-doped carbon composite system. Full article

The hematite phase decorated with iron-doped cerium oxide nanoparticles (F@FC) was precipitated from cerium and iron oxalate intermediate products. The photocatalytic composite of graphitic carbon nitride (gCN) and F@FC was prepared by a simple method involving mixing the two components, followed by thermal treatment at 400 °C. According to electron microscopy, F@FC is composed of a submicron iron oxide (hematite) phase decorated with iron-doped cerium oxide nanoparticles deposited on gCN substrate. A hierarchically structured composite was observed instead of a simple mechanical mixture of α-Fe₂O₃, Fe-CeO₂, and gCN. To observe two types of degradation activity, photocatalytic and Photo-Fenton degradation activity, Rhodamine B (RhB) was applied as the model water pollutant. The influence of the amount of photocatalyst, the RhB concentration, the presence of cations and anions, the pH, and the effect of e⁻, h⁺, •OH, and •O₂⁻ scavenging reactants were studied. The Photo-Fenton degradation exhibited high efficiency across the entire tested pH range, whereas photocatalytic degradation showed comparable activity only at acidic pH. The F@FC-gCN composite catalyst exhibited a high degree of recyclability. The degradation pathways of photocatalytic and Photo-Fenton reactions were suggested by HPLC-MS analysis of the reaction products. A notable finding of this study was the observation that the green-yellow, fluorescent intermediate Rhodamine 110 was formed during the photocatalytic degradation of RhB. However, the high reactivity of the generated •OH radicals during Photo-Fenton degradation has been demonstrated to inhibit the formation of intermediate Rhodamine 110. Full article

Lithium-ion batteries (LIBs) can considerably improve their lifespan by optimising operating conditions. This may entail ensuring optimal operating temperature, limiting the state-of-charge (SoC) window, reducing cycling current, and changing the physical orientation of the uncompressed LIB cell. In this study, we examine how these four conditions and some of their combinations impact degradation in both 1st life as well as in second life. The cell analysed in this investigation was the Xalt 31 HE cell, an energy-optimised Li-ion pouch cell with a capacity of 31 Ah and an NMC433-graphite chemistry. As a follow-up study of previously reported results, a total of 18 cells were investigated. We report results focusing on improving cycle life and ensuring safety before second life. The optimal conditions for first-life cycling in the full SoC window were found at room temperature, when cycled with a lower current and the cells oriented horizontally. We observed that under the same cycling conditions, a vertical alignment of cells resulted in an increased degradation rate compared to horizontal alignment. The best second-life capacity retention was found for cells initially cycled at room temperature, then later cycled with a reduced SoC window, at a lower current and in a horizontal orientation. If the cells were cycled at an elevated temperature in first life, the second-life compatibility was reduced considerably. An incremental capacity analysis (ICA) of the first-life ageing data revealed a possible indicator for ensuring safety and cycleability into second-life use. Full article

The development of lithium-ion batteries (LIBs) capable of extreme fast charging (XFC) while preserving safety, durability, and practical energy density remains a central challenge for next-generation electric transportation and grid-scale storage. Conventional graphite anodes are fundamentally limited at high current densities by sluggish intercalation kinetics, which cause lithium plating, motivating the exploration of alternative insertion materials. This review provides a comprehensive and internally consistent assessment of titanium-based oxide anodes, encompassing TiO₂ polymorphs, lithium titanate (Li₄Ti₅O₁₂), and Wadsley–Roth titanium niobium oxides, through the combined lenses of crystal topology, diffusion pathways, redox chemistry, interfacial behavior, and resource scalability. By systematically comparing structural frameworks and electrochemical mechanisms across these material classes, we demonstrate that fast-charging performance is governed not by nano-structuring alone, but by the intrinsic coupling between operating potential, framework rigidity, and multi-electron redox activity. While Li₄Ti₅O₁₂ establishes the benchmark for safety and cyclability, and TiO₂ polymorphs provide structural versatility, titanium niobium oxides uniquely reconcile high theoretical capacity with minimal lithiation strain and open diffusion channels, positioning them as highly promising candidates for sub-10 min charging without catastrophic degradation. This review highlights the persistent obstacles these materials suffer, such as limited round-trip energy efficiency (RTE), interfacial gas evolution, poor dopant stability, and unsustainable extraction, while simultaneously exploring targeted design strategies to overcome them. Finally, this review provides a materials design and comparison framework for the development of safe, high-power, and commercially viable ultrafast-charging LIBs. Full article

This study investigated the extraction of aluminum from aluminum silicate-rich coal ash from the ash-slag waste of the Almaty CHP-2 power station using microwave-assisted alkaline leaching. The high chemical stability of the quartz and mullite phases in the ash leads to high energy consumption during conventional acid–base treatment. To improve the kinetic parameters of the leaching process, amorphous graphite was therefore used as an active additive, which effectively absorbs microwave energy. The experiments were conducted in the temperature range of 50–200 °C, in 1–6 M NaOH solution, and over a period of 5–30 min. The amount of amorphous graphite varied between 5 and 20 wt%. The proportion of amorphous graphite varied between 5 and 20 wt%. Upon microwave irradiation, the graphite-free ash reached a temperature of 200 °C within approximately 12 min, whereas this temperature was reached in the system with 15% amorphous graphite after only 8–9 min. At low alkali concentrations (1–2 M NaOH), the aluminum transfer into solution in the graphite-free system was approximately 18%–35%. With increasing NaOH concentrations to 3–4 M, the aluminum removal efficiency increased to 38%–58%. Under the same temperature conditions, the leaching process was significantly accelerated by the addition of amorphous graphite; thus, at temperatures near 200 °C and in a 5–6 M NaOH solution, 70%–72% of aluminum was removed. The leaching kinetics were analyzed using the shrinking core model. The results showed that the apparent activation energy of the reaction decreased from 54 kJ/mol to 32 kJ/mol in the presence of graphite. These results suggest that microwave-assisted alkaline leaching in the presence of amorphous graphite is an energy-efficient and promising method for aluminum recovery from coal ash. Full article

Diamond antireflection techniques are of high interest for optical windows operating at extreme conditions. Herein, diamond antireflective microstructures in mid-infrared (MIR) spectral range were theoretically designed and experimentally fabricated. Finite difference time domain (FDTD) simulations were used to optimize the transmission performance of the diamond microstructures. Based on the simulation results, the optimized microstructures were fabricated by femtosecond (fs) laser direct writing (1030 nm, 300 fs, 25 kHz) followed by wet etching. After wet etching, the laser-modified zones and the accumulated graphitized clusters were effectively removed, thereby achieving the desired depth. The influences of laser power and scanning strategy on the morphology evolution of diamond microstructures were investigated. It was found that at the optimal conditions, the transmittance of the diamond increased from 70.9% to 81.4% (single-side) over a broad spectrum from 8 to 22 μm. This work demonstrates a promising hybrid fs laser/wet etching technique for diamond antireflective microstructures in MIR spectral range. Full article

Hexagonally ordered mesoporous carbon was ozonized, and the oxidized carbonaceous material was modified with L-arginine. The ozonized and L-arginine-modified carbons were extensively characterized and tested as Pb(II) ion adsorbents, with optimization of Pb(II) solution pH, exposure time, Pb(II) ion concentration and the presence of concurrent ions. Pb(II) adsorption equilibrium was achieved within 5 min at optimal pH = 2.6 or 5.3 for the oxidized and L-arginine-modified carbonaceous materials, respectively. The adsorption kinetics of both investigated materials were best described by the pseudo-first-order model. The maximum adsorption capacity for Pb(II) ions was determined to be 16 mg g⁻¹ (ozonized material) or 45 mg g⁻¹ (L-arginine-modified material). The Langmuir model provided the best fit for the adsorption isotherm data. Fe(III) ions mostly hindered the Pb(II) adsorption (up to 60%) on the L-arginine-modified carbon material. L-arginine-modified carbon was used to enrich Pb(II) from simulated urban roof runoff and its determination using the slurry sampling high-resolution continuum-source graphite furnace atomic absorption spectrometry technique. The developed analytical procedure was characterized by a limit of quantification of 2.63 µg L⁻¹, an enrichment factor of 50, and a recovery rate of 94.8%. Full article

Sustainable materials are increasingly being incorporated into high-strength concrete (HSC) to reduce environmental impact while maintaining structural performance. This study experimentally investigates the combined use of steel scale waste (SSW) as a replacement for natural fine aggregates and graphite nano/micro platelets (GNMPs) as a nano-modifying additive in HSC. Natural sand was replaced with SSW at levels of 0%, 50%, and 100%, while GNMPs were incorporated at dosages of 0%, 0.1%, 0.3%, and 0.5% by weight of cement. The results indicate that partial replacement of sand with SSW significantly improves concrete density and mechanical performance due to enhanced particle packing and the high specific gravity of steel scale particles. At the nanoscale, GNMPs contribute to pore refinement, improved nucleation of hydration products, and crack-bridging within the cement matrix, thereby strengthening the interfacial transition zone and delaying crack propagation. The combined effect of these mechanisms produces a synergistic enhancement in concrete performance. The optimum mixture containing 50% SSW and 0.3% GNMPs achieved a compressive strength of 68.2 MPa and splitting tensile strength of 7.6 MPa, representing improvements of approximately 54% and 52%, respectively, compared with the control mix. Durability-related properties such as water absorption and sorptivity were also significantly improved due to matrix densification and pore structure refinement. Although the incorporation of SSW and GNMPs reduced workability, all mixtures remained within a practical range for casting. The developed concrete is particularly suitable for structural applications requiring high strength and durability, such as high-rise building components, bridge elements, and precast structural members. The findings demonstrate that the combined use of industrial steel waste and nano-reinforcement offers a promising pathway toward sustainable and high-performance concrete. Full article