Search Results (260)

In this study, a novel low-temperature (300–500 °C) carbothermal reduction route employing potassium ferrate and sodium hydroxide was developed to synthesize magnetic zero-valent iron-doped biochar for removing tetracycline and ciprofloxacin from aqueous solutions. Carbothermal reduction occurred effectively at 400 °C, generating sufficient small reductive molecules for the reduction of iron species into zero-valent iron. This process led to the impregnation of abundant zero-valent iron along with nano-magnetite into the carbon matrix, while nano-magnetite was also dispersed and stabilized on zero-valent iron. Simultaneously, abundant functional groups were formed, contributing to anchoring iron species and adsorbing pollutants. The magnetic biochar exhibited high adsorption capacities for tetracycline (1106.25 mg/g) and ciprofloxacin (182.03 mg/g), along with high saturation magnetization (56.3 emu/g) and superior reusability. Moreover, the magnetic biochar showed broad applicability for efficient removal of tetracycline and ciprofloxacin derivatives. Overall, carbothermal reduction efficiently transformed iron oxides into zero-valent iron at a relatively low temperature, providing a viable approach for manufacturing magnetic biochar doped with zero-valent iron. Full article

Lithium–iron disulfide (Li-FeS₂) batteries are plagued by the polysulfide shuttle effect and cathode structural degradation, which significantly hinder their practical application. This study proposes a dual-strategy design that combines a polyacrylonitrile–carbon nanotube (PAN-CNT) composite cathode and a polyvinylidene fluoride (PVDF)-conductive carbon-coated separator to synergistically address these bottlenecks. The PAN-CNT binder establishes chemical anchoring between polyacrylonitrile and FeS₂, enhancing electronic conductivity and mitigating volume expansion. Specifically, the binder boosts the initial discharge capacity by 35% while alleviating the stress-induced pulverization associated with volume changes. Meanwhile, the PVDF-conductive carbon-coated separator enables effective polysulfide trapping via dipole–dipole interactions between PVDF’s polar C-F groups and Li₂S_x species while maintaining unobstructed ion transport with an ionic conductivity of 1.23 × 10⁻³ S cm⁻¹, achieving a Coulombic efficiency of 99.2%. The electrochemical results demonstrate that the dual-modified battery delivers a high initial discharge capacity of 650 mAh g⁻¹ at 0.5 C, with a capacity retention rate of 61.5% after 120 cycles, significantly outperforming the control group’s 47.5% retention rate. Scanning electron microscopy and electrochemical impedance spectroscopy confirm that this synergistic design suppresses polysulfide migration and enhances interfacial stability, reducing the charge transfer resistance from 26 Ω to 11 Ω. By integrating polymer-based functional materials, this work presents a scalable and cost-effective approach for developing high-energy-density Li-FeS₂ batteries, providing a practical pathway to overcome key challenges in their commercialization. Full article

This study investigated the dynamic resolution of lexical–semantic ambiguity during sentence comprehension, focusing on how uncertainty evolves as contextual information accumulates. Using time-resolved eye-tracking and a novel entropy-based measure derived from group-level semantic choice distributions, we quantified semantic uncertainty at a fine-grained temporal resolution for ambiguous words. By parametrically manipulating the semantic bias strength of the sentence context, we examined how context guides disambiguation over time. The results showed that semantic uncertainty declined gradually over temporal segments and dropped sharply following the onset of ambiguous words, reflecting both incremental integration and syntactic anchoring. A stronger contextual bias led to faster reductions in uncertainty, with effects following a near-linear trend. These findings support dynamic semantic processing models that assume continuous, context-sensitive convergence toward intended meanings. In contrast, a pretrained Chinese BERT model (RoBERTa-wwm-ext) showed similar overall trends in uncertainty reduction but lacked sensitivity to contextual bias. This discrepancy suggests that, while language models can approximate human-level disambiguation broadly, they fail to capture fine-grained semantic modulation driven by context. These findings provide a novel empirical characterization of disambiguation dynamics and offer a new methodological approach to capturing real-time semantic uncertainty. The observed divergence between human and model performance may inform future improvements to language models and contributes to our understanding of possible architectural differences between human and artificial semantic systems. Full article

(1) Background: Virtual Reality (VR) films challenge traditional visual cognition by offering novel perceptual experiences. This study investigates the applicability of Gestalt grouping principles in dynamic VR scenes, the influence of VR environments on grouping efficiency, and the relationship between viewer experience and grouping effects. (2) Methods: Eye-tracking experiments were conducted with 42 participants using the HTC Vive Pro Eye and Tobii Pro Lab. Participants watched a non-narrative VR film with fixed camera positions to eliminate narrative and auditory confounds. Eye-tracking metrics were analyzed using SPSS version 29.0.1, and data were visualized through heat maps and gaze trajectory plots. (3) Results: Viewers tended to focus on spatial nodes and continuous structures. Initial fixations were anchored near the body but shifted rapidly thereafter. Heat maps revealed a consistent concentration of fixations on the dock area. (4) Conclusions: VR reshapes visual organization, where proximity, continuity, and closure outweigh traditional saliency. Dynamic elements draw attention only when linked to user goals. Designers should prioritize spatial logic, using functional nodes as cognitive anchors and continuous paths as embodied guides. Future work should test these mechanisms in narrative VR and explore neural correlates via fNIRS or EEG. Full article

To achieve dual functionality that can monitor both Al³⁺ levels in food and the freshness of fish, rice straw fibers (RSFs) were treated in NaOH solutions and then cationized with 2,3-epoxypropyltrimethylammonium chloride, onto which alizarin red S molecules were immobilized through electrostatic interaction to develop a smart felt-like label. An optimized treatment in 5 wt% NaOH solution effectively removed lignin and hemicellulose, facilitating quaternary ammonium group grafting and stable ARS anchoring. The ARS@BRSF-5NaOH exhibited high pH sensitivity, showing visually discernible color changes (ΔE > 5, perceptible to the naked eye) under acidic (pH ≤ 6) and strongly alkaline (pH > 12) conditions. During the storage of the fish, the label transformed from yellow to dark purple (ΔE increase) as TVB-N levels approached 20 mg/100 g, enabling real-time freshness monitoring for protein-rich products. Additionally, the label achieved a detection threshold of 1 × 10⁻⁵ mol·L⁻¹ for Al³⁺ through a coordination-induced chromatic transition (purple to pale pink). This research highlights the feasibility of utilizing an agricultural waste-derived material to develop cost-effective, visually responsive, dual-functional intelligent labels for food safety, offering significant advancements in on-site quality assessment. Full article

The recovery and control of volatile organic compounds (VOCs) have gained significant attention. Supported sulfonic acid materials show potential in converting aromatic VOCs into non-volatile sulfonic acid derivatives. However, their effectiveness is closely tied to the anchoring state of the sulfonic acid groups. In this study, two supported sulfonic acids, SSA@CdO and SSA@CaO, were synthesized via the respective reactions of CdO and CaO with chlorosulfonic acid to investigate how the properties of the supports influence sulfonic acid anchoring and reactivity toward o-xylene. Comprehensive characterization and performance tests revealed that sulfonic acid groups on CdO were covalently bonded, forming positively charged sites ([O_0.5Cd–O]^ɗ−–SO₃H^ɗ+) with high loading (9.7 mmol/g), enabling excellent o-xylene removal (≥95.6%) and adsorption capacity (51.67–91.59 mg/g) at 130–150 °C. In contrast, ion-paired bonding on CaO formed negatively charged sites ([O_0.5Ca]⁺:OSO₃H⁻), which were inactive in electrophilic sulfonation. This work provides new insights for enhancing supported sulfonic acid materials in VOC treatment. Full article

Aryl diazonium salt chemistry offers a robust and versatile approach for the modification of material surfaces via the covalent immobilization of reactive functional groups under mild conditions. In this study, this strategy was successfully applied to graft the chelating agent 4-(2-pyridylazo)resorcinol (PAR) onto Amberlite XAD-4 resin. Initially, 4-nitrobenzenediazonium tetrafluoroborate (NBDT) was covalently anchored onto the resin surface using hypophosphorous acid as a reducing catalyst to introduce aryl nitro groups. These nitro groups were subsequently reduced to aniline functionalities, enabling diazo coupling with PAR. The successful modification of the resin was confirmed by ATR-FTIR spectroscopy, thermogravimetric analysis (TGA), and X-ray photoelectron spectroscopy (XPS). The synthesized chelating resin exhibited sorption capacities of 0.152, 0.167, and 0.172 mM g⁻¹ for Co(II), Ni(II), and Cu(II), respectively. The functionalized resin was packed into standard SPE cartridges and employed as a selective sorbent for the extraction and preconcentration of trace metals from groundwater samples collected from Dhalamah Valley, Al-Madinah Al-Munawwarah, prior to quantification by inductively coupled plasma mass spectrometry (ICP-MS). These results demonstrate the effectiveness of rapid diazonium-based surface functionalization for the preparation of selective polymeric metal chelators suitable for the extraction of trace metals from complex groundwater matrices. Full article

The conversion of cellulosic biomass into renewable chemicals can serve as a sustainable resource for levulinic acid (LA) production. LA yield is significantly influenced by reaction temperature, reaction time, substrate concentration, active sites, catalyst amount, catalyst porosity, and durability. Beyond the features of the catalyst, such as acidity, porosity, functional groups, and catalytic efficiency, the contact between the solid acid catalyst and the solid substrate is of vital importance. Solid-based catalysts show remarkable catalytic activity for cellulose-derived LA production, thanks to the incorporation of functional groups. For a solid carbon-based catalyst to be effective, a synergistic interaction between the binding domain (functional groups capable of anchoring cellulose to the catalyst surface, such as chloride groups, COOH, or OH) and the hydrolysis domain (due to their ability to cleave glycosidic bonds, such as in SO₃H) is essential. As a relatively new market niche, carbon-based catalyst supports are projected to reach a market value of nearly USD 125 million by 2030. This review aims to highlight the advantages and limitations of carbon-based materials compared to conventional catalysts (including metal oxides or supported noble metals, among others) in features like catalytic activity, thermal stability, and cost, examine recent advancements in catalyst development, and identify key challenges and future research directions to enable more efficient, sustainable, and scalable processes for LA production. The novelty of this review lies in its focus on carbon-based catalysts for LA production, emphasizing their physical and chemical characteristics. Full article

To address the issue of drilling fluid performance drop and wellbore instability induced by desorption between treatment agents and clay in the high-temperature environment of ultra-deep drilling, this study synthesized three organosilicon polymers (ADE, ADM, ADD) with different substituents. The study confirmed that the covalent bond significantly improved the high-temperature adsorption resistance of clay, which is closely related to the interface behavior of gels. Through rolling recovery, rheology, and filtration experiments for performance evaluation, these organic silicon polymers showed excellent high-temperature performance: the shale rolling recovery rate exceeded 80% at 210 °C, and the filtration loss was reduced to 14 mL, with a reduction rate of 53.3%. The adsorption capacity of the three polymers on clay remained unchanged from 150 °C to 210 °C, among which the adsorption amount of trimethoxy groups stabilized at 8–11 mg/g after 150 °C. The adsorption capacity of ethoxy groups increased by 7.9% at 150–210 °C. The adsorption capacity of dimethoxy groups with methyl steric hindrance increased by 28.1% at 150–210 °C. These results indicate that covalent bonds effectively enhance the high-temperature adsorption of clay, allowing for polymer molecules to firmly anchor on the clay surface at high temperatures. This breakthrough overcomes the limitations of traditional inhibitors in high-temperature desorption, and provides a valuable reference for the preparation of high-temperature adsorption resistant functional materials in water-based drilling fluid gel systems. Full article

Background/Objectives: This study investigated the association between cochlear implant (CI) users’ assessed perception of musical sound quality and their subjective music perception and music-related quality of life (QoL). The aim was to provide a comprehensive evaluation by integrating a relatively objective Turkish Multiple Stimulus with Hidden Reference and Anchor (TR-MUSHRA) test and a subjective music questionnaire. Methods: Thirty CI users and thirty normal-hearing (NH) adults were assessed. Perception of sound quality was measured using the TR-MUSHRA test. Subjective assessments were conducted with the Music-Related Quality of Life Questionnaire (MuRQoL). Results: TR-MUSHRA results showed that while NH participants rated all filtered stimuli as perceptually different from the original, CI users provided similar ratings for stimuli with adjacent high-pass filter settings, indicating less differentiation in perceived sound quality. On the MuRQoL, groups differed on the Frequency subscale but not the Importance subscale. Critically, no significant correlation was found between the TR-MUSHRA scores and the MuRQoL subscale scores in either group. Conclusions: The findings demonstrate that TR-MUSHRA is an effective tool for assessing perceived sound quality relatively objectively, but there is no relationship between perceiving sound quality differences and measures of self-reported musical engagement and its importance. Subjective music experience may represent different domains beyond the perception of sound quality. Therefore, successful auditory rehabilitation requires personalized strategies that consider the multifaceted nature of music perception beyond simple perceptual judgments. Full article

The inherent hydrophobic nature of PVDF material renders it challenging to establish a stable aqueous hydration layer, thereby limiting its suitability as a substrate for the preparation of nanofiltration (NF) membranes. In this study, we developed a novel modification approach that effectively enhances the hydrophilicity of PVDF substrates through the incorporation of sulfonic acid-doped polyaniline (SPANI) and hyperbranched polyester (HPE) into the PVDF casting solution, followed by cross-linking with trimesoyl chloride (TMC). The introduction of SPANI and HPE, which contain reactive polar amino and hydroxyl groups, improved the hydrophilicity of the substrate, while the subsequent cross-linking with TMC effectively anchored these components within the substrate through the covalent linking between TMC and the reactive sites. Additionally, the hydrolysis of TMC yielded non-reactive carboxyl groups, which further enhanced the hydrophilicity of the substrate. As a result, the modified PVDF substrate exhibited improved hydrophilicity, facilitating the construction of an intact polyamide layer. In addition, the fabricated TFC NF membrane demonstrated excellent performance in the advanced treatment of tap water, achieving a total dissolved solid removal rate of 57.9% and a total organic carbon removal rate of 85.3%. This work provides a facile and effective route to modify PVDF substrates for NF membrane fabrication. Full article

Drag embedment anchors (DEAs) provide reliable and cost-effective mooring solutions for floating structures, e.g., platforms, ships, offshore wind turbines, etc., in offshore engineering. Structural stability and operational safety require accurate predictions of their penetration depths and holding capacities across various seabed conditions. In this study, explicit linear regression (LR) models were developed for the first time to predict the penetration depth and holding capacity of DEAs on clay and sand seabed. Buckingham’s theorem was also applied to identify dimensionless groups of parameters that influence DEA behavior, e.g., the penetration depth and holding capacity of the DEAs. LR models were developed and validated against experimental data from the literature for both clay and sand seabed. To evaluate model performance and identify the most accurate LR models to predict DEA behavior, comprehensive sensitivity, error, and uncertainty analyses were performed. Additionally, LR analysis revealed the most influential input parameters impacting penetration depth and holding capacity. Regarding offshore mooring design and geotechnical engineering applications, the proposed LR models offered a practical and efficient approach to estimating DEA performance across various seabed conditions. Full article

This article investigates issues in the local operationalization of the Planetary Boundaries concept (PBc), crucial for assessing human impacts on the Earth system and guiding sustainable development policies. Originally designed for the global scale, this concept requires local adaptation to align territorial actions with global environmental goals. Following a qualitative analysis of 34 review articles, a systematic categorization method is employed to identify recurrent localization and operationalization issues. Their analysis provides three main contributions that improve the understanding of PBc downscaling mechanisms. First, it identifies a prevalent quantification-based localization approach. Second, it categorizes local operationalization constraints into three distinct groups. Third, it reveals underlying patterns demonstrating that the prevalent approach, despite ensuring scientific rigor, generates methodological and practical constraints to effective local operationalization. This “operational paradox” reveals fundamental tensions between the PBc’s biophysical interpretation, localization by quantification, and local operationalization, contrasting measurement or meaning, precision or participation, and standardized solutions or locally adapted responses. For future research, the analysis of the interactions between these contributions suggests operating a paradigm shift based on a socio-biophysical interpretation of the PBc and the contextualization of the resulting components. This alternative approach could prioritize territorial anchoring, stakeholder inclusion, and the co-construction of sustainability trajectories. Full article

The contribution of the environment to protein folding seems obvious. The aqueous environment directs protein folding towards generating a centric hydrophobic core with a polar shell. The cell membrane environment—in which numerous proteins are anchored—to stabilise the arrangement, expects the exposure of hydrophobic residues and the concentration of polar residues in the central part—a channel for the transport of numerous molecules. The influence of these environments seems evident due to the persistent residence of proteins in their surroundings providing an external force field for structure stabilisation. Structural forms are also obtained with the participation of supporting proteins—such as proteins from the heat shock protein group—which accompany the folding process and temporarily provide an appropriate external force field in which the protein, having obtained the correct structure for its activity, is released from interaction with the supporting protein. This paper discusses an example of the contribution of Hsp104 to casein folding and the effect of disaggregase preventing inappropriate aggregation. For this purpose, a model called the fuzzy oil drop (FOD-M) was used, which takes hydrophobic interactions into account in the assessment of protein structure status. Their distribution in the protein body highlights the contribution and influence of the external force field—originating from Hsp104 and the disaggregase in this case. Full article

To successfully prepare cellulose hydrogels through a dissolution–regeneration process, 60 wt% LiBr aqueous solution was used as a green solvent. Carboxyl groups were precisely introduced onto the surface of the cellulose hydrogels through a TEMPO-mediated oxidation reaction, while the three-dimensional network structure and open pore morphology were completely retained. This modification strategy significantly enhanced the loading capacity of the hydrogels with copper nanoparticles (Cu NPs). The experimental results show that the LiBr aqueous solution can efficiently dissolve cellulose, and the TEMPO oxidation introduces carboxyl groups without destroying the stability of the hydrogels. Cu NPs are uniformly dispersed and highly loaded on the surface of the hydrogel because of the anchoring effect of the carboxyl groups. Cu NP-loaded hydrogels exhibit excellent catalytic activity in the NaBH₄ reduction of 4-nitrophenol (4-NP). Cu NP-loaded hydrogels maintain their complete structure and good catalytic performance after five consecutive cycles. Moreover, Cu NP-loaded hydrogels demonstrate high efficiency in degrading organic dyes such as methyl orange and Congo red. This study successfully developed efficient, low-cost, and environmentally friendly Cu NP-loaded hydrogel catalysts through the synergistic effect of LiBr green solvent and TEMPO oxidation modification, providing a feasible alternative to noble metal catalysts. Full article