Search Results (261)

This study investigates the synthesis and kinetic behavior of a magnetic biochar derived from avocado seed biomass for the removal of hexavalent chromium (Cr(VI)) from aqueous solutions. Magnetite (Fe₃O₄) was synthesized through different routes, including nitrogen-assisted coprecipitation, redox-controlled coprecipitation, polyol, sol–gel, and sonochemical methods, to evaluate their structural properties and iron incorporation efficiency. Based on compositional and crystallographic analyses, the coprecipitation under an inert atmosphere exhibited improved phase purity and higher Fe₃O₄ content, which was selected for in situ incorporation onto biochar produced by pyrolysis at 450 °C. The resulting magnetic material and composite were characterized using X-ray diffraction (XRD), X-ray fluorescence (XRF), Fourier-transform infrared spectroscopy (FTIR), and scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM–EDS), confirming the suitability of the synthesis method and the successful deposition of magnetite onto the porous carbon matrix while preserving its structural integrity. Batch adsorption experiments were conducted at pH 2.0 to evaluate the effect of adsorbent dose and initial Cr(VI) concentration. The adsorption process reached equilibrium within 120 min and was better described by the pseudo-second-order kinetic model (R² ≥ 0.98), suggesting that chemisorption governs the rate-controlling step, with diffusion phenomena contributing but not dominating the overall mechanism. The maximum adsorption capacity predicted by the kinetic model reached 42.49 mg g⁻¹ at an initial concentration of 100 mg L⁻¹. The results demonstrate that avocado-seed-derived magnetic biochar represents a sustainable and effective material for chromium-contaminated water treatment, integrating agro-industrial waste valorization with enhanced adsorption performance and magnetic separability. Full article

The performance of remote sensing-based mineral alteration extraction is significantly restricted in the vegetation area. Spectral unmixing is one of the effective methods to address the vegetation problem during mineral alteration extraction. However, the spectral curves of different tree species vary a lot; if multiple tree species are regarded as a whole during the spectral unmixing stage, the proportions of vegetation would be estimated with more errors. The purpose of this study was to verify the effects of dominant tree species classification on spectral unmixing and reconstruction, and to apply the proposed method to the mineral alteration extraction practice. To accomplish this, the Shabaosi gold deposit region in Mohe City, China, with an area of 650 km², was selected as the study area. Firstly, reference spectral curves, GaoFen-1/6 (GF-1/6) satellite imageries, ZiYuan-1F (ZY-1F) satellite imageries, Sentinel-1B satellite synthetic aperture radar (SAR) data, the ALOS digital elevation model (DEM), and sub-compartment dominant tree species data were collected; subsequently, simulated mixed-pixel reflectance images of ZY-1F, reflectance images of GF-1/6, ZY-1F, backscattering data of Sentinel-1B, slope, aspect, and 5484 tree species samples were derived from the collected data. Secondly, to verify the effect of dominant tree species classification on mineral alteration extraction, the reference spectra of pine, oak, goethite, and kaolinite were used to construct a simulated ZY-1F mixed-pixel image, and spectral unmixing and reconstruction experiments were conducted. Thirdly, fourteen independent variables were selected from the derived data, five dominant tree species classification models were trained and tested using tree species samples via the ResNet50 algorithm, and the pine- and birch-dominated parts were segmented from the ZY-1F images. Fourthly, minimum noise fraction (MNF), pixel purity index (PPI), n-dimensional visualizer auto-clustering, and spectral angle mapper (SAM) methods were separately applied to the pine- and birch-dominated parts of ZY-1F images to extract and identify endmembers; subsequently, the fully constrained least squares (FCLS) and linear spectral unmixing (LSU) methods were separately applied to the pine- and birch-dominated parts to estimate endmember proportions and generate spectrally reconstructed ZY-1F images. Fifthly, the pine- and birch-dominated parts of spectrally reconstructed ZY-1F images were mosaiced, and the SAM was utilized to extract mineral alteration in the study area. The result showed that in the spectral unmixing and reconstruction experiment, the spectral reconstruction error declined from 0.0594 (simulated ZY-1F image without segmentation) to 0.0292 and 0.0388 (simulated ZY-1F image that was segmented by pine- and oak-dominated parts), suggesting that dominant tree species classification could improve the accuracy of spectral unmixing and reconstruction and help obtain a more reliable mineral alteration extraction result. In the study area, the tested overall accuracies (OA) and Kappa coefficients of the five dominant tree species classification models were 0.75 ± 0.03 and 0.50 ± 0.05, respectively, suggesting that conducting dominant tree species classification was feasible in dense vegetation areas and could facilitate mineral alteration extraction. After segmenting the ZY-1F image by pine- and birch-dominated parts and spectral reconstruction, eight main types of alteration, including kaolinite, vesuvianite, montmorillonite, rutile, limonite, mica, sphalerite, and quartz, were identified, and nine mineral alteration areas (MA) were delineated accordingly. Full article

This study addresses the issue of insufficient product purity caused by the co-deposition of three major impurity ions—zinc, nickel, and lead—during the electrodeposition process of high-purity manganese. A targeted deep purification method for manganese sulfate electrolyte was developed using dithiocarbamate chelating agents (sodium dimethyldithiocarbamate, SDD). By optimizing key process parameters such as precipitant concentration, reaction temperature, reaction time, and solution pH, combined with density functional theory (DFT) calculations, to elucidate the selective impurity removal mechanism at the molecular level, a novel process for the efficient synergistic removal of Zn²⁺, Ni²⁺, and Pb²⁺ was established. The results showed that under the conditions of precipitant concentration of 1 g/L, solution pH of 6.5, reaction temperature of 55 °C, and reaction time of 2 h, the residual concentrations of Zn, Ni, and Pb in the electrolyte were all below 0.2 mg/L. DFT calculations revealed that SDD coordinates with metal ions through four sulfur atoms, and the absolute values of binding energies follow the order Ni²⁺ > Pb²⁺ > Zn²⁺ > Mn²⁺, indicating thermodynamically preferential capture of impurity ions. After purification, the manganese metal obtained by electrodeposition from the manganese sulfate solution achieved a purity exceeding 99.999%, with Zn, Ni, and Pb contents of 0.11 mg/kg, 0.038 mg/kg, and 0.05 mg/kg, respectively, meeting the raw material requirements for semiconductor-grade copper–manganese alloy targets. Full article

The practical application of inorganic ferroelectric fillers in flexible piezoelectric composites is critically constrained by low polarization efficiency and severe interfacial incompatibility with polymer matrices. Herein, we report a multi-level in situ surface modification strategy that simultaneously addresses both limitations. High-purity one-dimensional tetragonal barium titanate nanofibers (BTO NFs) are first synthesized via sol–gel electrospinning combined with a two-step gradient annealing process, which precisely controls phase evolution and preserves structural continuity. To overcome the detrimental acid-induced degradation of BTO NFs during functionalization, a polydopamine (PDA) buffer layer is first conformally coated, followed by the liquid-phase deposition of a conductive polypyrrole (PPy) shell, forming a robust core–shell PPy@PBT NFs architecture. Incorporating only 4 wt% of these multifunctional fillers into a poly(vinylidene fluoride) (PVDF) matrix yields a dramatic enhancement in electromechanical performance. The resulting flexible piezoelectric energy harvesters achieve a piezoelectric coefficient (d₃₃) of 28.7 pC/N, an output voltage of 13 V, and an output current of 0.7 μA, representing substantial improvements over unmodified filler systems. This synergistic enhancement originates from the PDA-mediated interfacial stress transfer and the PPy-induced Maxwell–Wagner polarization intensification, establishing a robust and generalizable paradigm for high-performance flexible piezoelectric composites in self-powered wearable electronics. Full article

The growing volume of fiber-reinforced polymer composite waste creates an urgent need for efficient recycling technologies. While solvolysis effectively breaks down thermoset matrices for fiber reinforcement recovery, the process generates hydrocarbon-rich liquid by-products that require further management. This study validates the use of these liquid recycling streams—derived from the solvolysis of unsaturated polyester and epoxy resins—as sustainable carbon precursors for the growth of carbon nanomaterials. Synthesis was performed via catalytic chemical vapor deposition (CVD) at 850 °C using iron nanoparticles impregnated on a zeolite substrate. Morphological analysis confirmed the production of one-dimensional nanostructures (carbon nanotubes/nanofibers), with average diameters below 100 nm. Raman spectroscopy revealed a high degree of graphitization, with I_D/I_G ratios ranging from 0.25 to 0.58, which is comparable to structures synthesized from conventional precursors. Thermogravimetric analysis (TGA) demonstrated high thermal stability and carbon purity reaching up to 90.3%. These findings demonstrate a viable upcycling pathway that enhances the economic attractiveness of composite recycling by transforming waste into advanced nanomaterials. Full article

Metal–organic chemical vapor deposition (MOCVD) is a crystal growth technique used to achieve high-purity thin films, especially III–V materials, for fabricating semiconductor devices. It allows for thickness tunability, controlled doping, and composition of epilayers. This review focuses on the principle of MOCVD, its historical background, and its applications in III–V semiconductor devices such as solar cells, high electron mobility transistors (HEMTs), light-emitting diodes (LEDs), laser diodes (LDs), and photonic integrated circuits (PICs). This review highlights the recent developments in MOCVD aimed at improving its efficiency, performance, and sustainability. Finally, we emphasize emerging trends and challenges in MOCVD process innovation, reactor design, and material integration that are poised to drive the development of next-generation optoelectronic, photonic, and quantum technologies. Together, these findings underscore MOCVD’s pivotal role in enabling high-performance devices and sustaining leadership in post-Moore semiconductor technologies. Full article

Type II collagen (CII), the major structural protein in the cartilage extracellular matrix, is a promising biomaterial for scaffold design in cartilage tissue engineering. In this study, high-purity CII was successfully extracted from bovine cartilage, an abundant by-product of cattle slaughter, and its amino acid composition, triple-helical conformation, and thermal stability were verified. CII was subsequently combined with silk fibroin (SF) and chitosan (CS) to fabricate three-dimensional (3D) porous scaffolds via freeze-drying. The pore structure, porosity, swelling behavior, mechanical properties and in vitro degradation characteristics were systematically evaluated. Scaffolds with favorable structural integrity, mechanical performance, and degradation rates were further evaluated biologically using human primary chondrocytes. All CII-based composite scaffolds supported chondrocyte growth and promoted early extracellular matrix deposition. Notably, the scaffold with a CII:SF:CS ratio of 7:3:1 showed the highest GAG/DNA content, accompanied by upregulated gene expression related to the cartilage phenotype (COL2A1, ACAN, and SOX9) and reduced expression of the dedifferentiation marker COL1A1, indicating improved phenotype maintenance. Overall, within the tested range, CII70 (CII:SF:CS = 7:3:1) represents a practical compromise between scaffold stability and in vitro chondrocyte-related outcomes, providing a basis for selecting CII/SF/CS formulations for cartilage tissue engineering. Full article

Aflatoxin B1 (AFB1) is one of the most toxic mycotoxins contaminating animal feed, and bentonite clays are widely used as adsorbents to reduce its bioavailability. This study introduces and characterizes a new, previously unexplored bentonite deposit from Bijelo Polje (Bar, Montenegro), with ~55% montmorillonite in the raw material. Size fractions (<0.200 mm, <0.037 mm, <0.005 mm) were obtained by sieving and centrifugation and characterized by laser diffraction, chemical composition, BET, CEC, and quantitative XRD (Rietveld). In vitro AFB1 adsorption (2–50 ppm, pH 3.0, 0.02% w/v adsorbent) simulated monogastric gastrointestinal conditions. Progressive size reduction increased smectite content (from ~55% to 91%), CEC (44–70 meq/100 g), purity, and BET specific surface area (26.5–50.8 m²/g), while reducing impurities and heavy metals to undetectable levels. The finest fraction (<0.005 mm) achieved the highest maximum adsorption capacity (q_max ≈ 240 mg/g), attributed to enhanced surface homogeneity and site accessibility, significantly outperforming coarser fractions and most unmodified natural bentonites. Only the <0.005 mm fraction fully complies with EU regulatory requirements (Commission Implementing Regulation (EU) No 1060/2013) for AFB1-binding feed additives (≥70% dioctahedral smectite, >90% binding, low quartz/calcite). These results demonstrate that simple mechanical fractionation can yield exceptional performance in a novel natural raw material, offering a cost-effective, sustainable alternative to chemical modification for mycotoxin mitigation. Full article

Ni thick films have a wide range of applications in mechanical areas for anti-corrosion, anti-friction and protection purposes, and are also extensively employed in the chip packaging field. Yet, the deposition of Ni thick films is still faced with many problems in deposition efficiency, dense structure and adhesion to the substrate. RF magnetron sputtering was employed to deposit on polished Ti substrate up to 10.8 µm thick Ni films at a high deposition rate (45 nm/min) in Ar atmosphere plus a small amount of H₂. Vacuum annealing was performed at 400 °C for 5 h. To characterize the adhesion via friction and scratch test, different loads were applied on both surfaces of as-sputtered and post-annealed Ni thick films, and results were comparatively analyzed. The films have high purity, compact structure, smooth surface and strong adhesion strength. Post-annealed samples showed better and stable adhesion of Ni thick films to the substrate surface. Full article

The generation of high-purity hydrogen via chemical reaction from hydrogen-rich materials is one of the ways in the alternative energy industry. In this approach, the utilization of catalytic materials that possess the capacity to initiate the decomposition of the starting material and the subsequent release of hydrogen is of paramount importance. In this study, nickel/cobalt-plated copper catalysts (NiCo/Cu) are presented, comprising from 4 to 90 wt.% of cobalt as catalytic materials for hydrogen generation via sodium borohydride (NaBH₄) hydrolysis reaction. The NiCo/Cu catalysts were synthesized via electroless deposition from glycine-based baths, utilizing Ni²⁺ and Co²⁺ ions as metal sources and morpholine borane (MB) as the reducing compound. The catalytic performance in alkaline NaBH₄ hydrolysis was found to correlate with the cobalt loading in the coating. The maximum rate of hydrogen production, which was determined to be 14.22 L min⁻¹ gcat⁻¹, was achieved at 343 K for a catalyst composed of 90 wt.% Co. The reaction proceeded with the activation energy of 52.5 kJ mol⁻¹, while the catalyst exhibited high durability, preserving nearly 88% of its initial activity after five successive reaction cycles. The combination of nickel and cobalt, along with their synergistic effect and high efficiency in the borohydride hydrolysis reaction, makes them promising catalysts. Full article

The existing forms and evolution mechanisms of carbon impurities constitute the core scientific issue in the optimization of polysilicon purification processes. The depth of research on this issue directly determines the targeting and effectiveness of directional impurity removal strategies, and is even a key prerequisite for improving the quality and reducing the cost of polysilicon products. Based on HSC simulation calculations and using the Gibbs free energy of reactions as the judgment criterion, this paper investigated the existing forms and evolution mechanism of carbon impurities during the production of polysilicon via the modified Siemens process. The results show that the evolution mechanism of carbon impurities is as follows: the solute carbon in silicon powder reacts with hydrogen to generate CH₄. Subsequently, CH₄ synergistically undergoes radical rearrangement and the Rochow reaction with methylchlorosilanes in chlorosilane and CH₄ in recovered hydrogen. Meanwhile, CH₃· radicals combine with radicals generated from chlorosilanes to form a mixture of methylchlorosilanes dominated by SiH(CH₃)Cl₂ as well as CH₄. After distillation purification, SiH(CH₃)Cl₂ enters the SiHCl₃ stream, and then synergistically undergoes cracking and radical rearrangement with CH₄ in high-purity hydrogen, the solid-soluble elemental carbon forms and deposits in polysilicon. Simultaneously, a mixture of methylchlorosilanes dominated by SiH(CH₃)Cl₂ along with CH₄ is generated and then fed into the tail gas system. This will provide the necessary theoretical foundation for the development of efficient and low-cost impurity removal strategies. Full article

Oxygen-focused ion beam induced deposition (O-FIBID) enables the direct-write fabrication of Pt nanostructures while simultaneously enhancing purity concurrently through reactive oxygen–deposit interactions. By systematically varying the dwell time, accelerating voltage, and precursor pressure, the Pt content and conductivity can be controlled. Under optimum conditions, the Pt content reached 63 at.%. Across the dwell-time range used for resistivity measurements, the Pt content increased from 20 to 33 at.%, while the resistivity decreased from 2.9 × 10⁴ μΩ·cm to 1.2 × 10³ μΩ·cm, which is consistent with enhanced percolation through Pt grains and the lower intrinsic resistivity of the purer Pt deposit. The simulation results support a purification mechanism driven by the beam-induced activation of implanted oxygen balanced against the preferential sputtering of Pt. These results demonstrate O-FIBID as a viable method for the nanoscale direct write of conductive Pt without post-processing, and some deviations from conventional FIBID wisdom are observed. These results serve as a foundation for exploring nascent, reactive focused ion beam-induced deposition processes. Full article

Following the discovery of therapeutic molecules and the identification of specific biological targets, preparation of regulatory dossiers entails extensive product development and characterization to support their safety, efficacy, and stability. We have examined the drug development and relevant regulatory considerations related to inhaled biological proteins in the accompanying article. This review focuses on the characterization of locally acting inhaled biological proteins. Drug product characterization is a regulatory requirement, and it ensures drug product safety, efficacy, stability, and usability by the target populations. Together, these two articles provide a comprehensive discussion based on our review and analysis of the available open literature. We have attempted to fill gaps and simulate discussion of challenges following sound scientific pathways. This approach has the prospect of addressing regulatory expectations leading to rapid solutions to unmet medical needs. The robustness of characterization strategies and the development of analytical methods used in the in vitro testing for the evaluation of drug product attributes is assured through application of the Design-of-Experiment (DOE) and Quality-by-Design (QBD) approaches. Drug product characterization entails a variety of in vitro studies evaluating drug products for purity and contamination, and determination of drug delivery by the intended route of administration. Measurement of the proportion of the labeled amount per dose and the form suitable for delivery to the intended target sites is central to this assessment. For respiratory Drug–Device combination products, the testing may vary with the product designs. However, determination of the single-dose content, delivered-dose uniformity, aerodynamic particle size distribution, and device robustness when used by the target populations is common to all combination products. Characterization of aerosol plumes is limited to inhalation aerosols that produce specific aerosol clouds upon actuation. The flow rate dependency of devices is also examined. Product characterization also includes safety-related product attributes such as degradation products and leachables. For inhaled biological proteins, safety-related in vitro testing includes additional testing to assure maintenance of the three-dimensional structural integrity and the sustained biological activity of the drug substance in the formulation, during aerosolization and upon deposition. This article discusses various tests employed for regulatory-compliant product characterization. In addition, the stability testing and handling of possible changes during product development and post-approval are discussed. Full article

Ammonium paratungstate (APT) was synthesized from scheelite ore concentrates from the Brejuí Mine in Currais Novos, Rio Grande do Norte, Northeast Brazil. The process involved acid leaching to obtain tungstic acid (H₂WO₄), followed by its conversion to APT. A 2³ factorial design evaluated the influence of temperature, HCl concentration, and reaction time on the leaching efficiency, revealing temperature and acid concentration as significant variables. Tungsten extraction reached 98.6% under moderate time and temperature conditions. The resulting H₂WO₄ phase exhibited a lamellar and porous morphology, facilitating its rapid dissolution and crystallization into APT at 60 °C. The produced nanometric APT exhibited high purity, a mixed rod-like/cubic morphology, and thermal stability above 600 °C. This work adds value to the Brazilian tungsten deposits by supporting more efficient and sustainable extraction routes for obtaining APT. Full article

A vacuum-arc pulsed plasma accelerator (APPA) operating at a discharge current of 750 A and a pulse duration of 110 μs with a repetition rate of 5 Hz was employed to deposit thin films and coatings under low- and medium-vacuum conditions. The aim of this study was to obtain metal coatings suitable for potential applications in the energy and chemical industries. SEM, AFM, and XRD techniques were used to investigate the structure and morphology of coatings formed on metallic and insulating substrates under the following conditions: residual pressure of 10⁻²–10⁻⁴ mbar and deposition times of 10–30 min. Under medium-vacuum conditions, thin and non-uniform metallic films with thicknesses ranging from 0.4 to 1.9 μm were deposited on metal substrates. The morphology of thick films deposited under low-vacuum conditions consisted of spherical metal particles of various sizes (0.1–1 μm), containing up to 30% carbon and 28% oxygen. On silicon substrates, spherical microparticles up to 4 μm in diameter with thin shells approximately 0.3 μm thick were formed. One possible mechanism for microsphere formation—the desorption of residual gases by the coating material—is discussed. The potential of the APPA method for producing metal shells, relevant to powder manufacturing due to the high energy density of the process and the intrinsic purity of vacuum technologies, is also considered. Porous coatings obtained using the APPA technique may be applicable in the fabrication of energy-related materials, such as battery anodes. Full article