Search Results (19,727)

Biochar provides a porous scaffold, conductive carbon framework and redox-active surface functional that can promote microbial attachment and extracellular electron flow. However, how feedstock-dependent biochar properties regulate the biochar–cell interface and microbial metabolism during contaminant removal remains insufficiently understood. Here, biochar derived from rice husk, corn straw and corn cob was used to immobilize Pseudomonas chlororaphis for triclocarban removal in batch microcosms. Multiscale analyses, including scanning electron microscopy (SEM), fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), cyclic voltammetry (CV), (electrochemical impedance spectroscopy (EIS) and liquid chromatography–mass spectrometryLC-MS, were combined to link the biochar structure, interface and extracellular metabolism signatures with triclocarban (TCC) removal. Compared with free cells, all composites enhanced TCC removal and exhibited altered interfacial functional-group features together with substantially reduced fitted charge-transfer resistance, indicating facilitated interfacial electron exchange. Untargeted metabolomics further revealed consistent remodeling of extracellular redox-associated metabolite signatures upon immobilization, with increased quinone/polyphenol-associated features and pathway-level shifts related to redox homeostasis. Among feedstocks, the corn cob composite showed the highest triclocarban removal. Overall, this work proposes an evidence-supported “structure–interface–metabolism” framework for interpreting how agricultural-residue biochars modulate biofilm interfaces and redox-related metabolic signatures to improve triclocarban removal, providing guidance for designing biochar-supported bioprocesses for halogenated micropollutants. Full article

This study investigates the influence of surface-modified carbon fibers (CFs) on the structural and mechanical properties of acrylonitrile-butadiene-styrene (ABS)-based composites. A comprehensive approach employing Fourier Transform Infrared Spectroscopy (FTIR), contact angle measurement, and thermogravimetric analysis (TGA) characterized the CF surface chemistry, wettability, and thermal stability. Specimens were prepared via injection molding and 3D printing processes, enabling systematic evaluation of tensile, flexural, and impact properties. Combined with Scanning Electron Microscopy observations of composite fracture surfaces, the study elucidates how modification treatments influence fiber–matrix interface bonding and mechanical enhancement mechanisms. The results indicate that after resizing treatment with silane coupling agents, the surface activity of CF and its interfacial compatibility with ABS were significantly improved, leading to a marked enhancement in the composite material’s overall performance. At a CF content of 9.62 wt%, the ABS-S-CF2 system exhibited optimal mechanical properties: The tensile strength and flexural strength of the injection-molded specimens reached 58.41 MPa and 81.51 MPa, respectively, representing increases of approximately 41.6% and 29.1% compared to neat ABS. The tensile strength and flexural strength of the printed specimens also reached 49.37 MPa and 80.19 MPa, respectively. Microstructural analysis indicates that the sizing treatment improves the interfacial bonding between CF and neat ABS. Full article

The resistance of pathogenic bacteria to antimicrobial agents is currently one of the most significant health challenges. Polymers and nano-polymer composites with antimicrobial properties are widely used, particularly in hospitals, biocompatible implants, and the medical device industry. Syzygium aromaticum (clove) contains several bioactive compounds, including potent antioxidants and antimicrobials, which confer antioxidant, antibacterial, and antiseptic properties. For this purpose, polyvinyl alcohol (PVA) films were produced at three different concentrations using a direct integration method and doped with clove essential oil. The spectral, structural, and thermal properties of the produced films were analyzed, and their antibacterial activity against Klebsiella pneumoniae was tested. Fourier Transform Infrared Spectroscopy (FTIR) results confirm that the structural integrity of the PVA matrix is preserved and that the essential oil is physically trapped within the polymer network. Overall, the Differential Scanning Calorimetry (DSC) results confirm that Syzygium aromaticum essential oil (SAEO) acts as an effective plasticizer in PVA films, significantly modifying the glass transition behavior and enhancing polymer chain mobility in a concentration-dependent manner. The Dynamic Mechanical Analysis (DMA) results, supported by DSC analysis, clearly demonstrate that SAEO acts as an effective plasticizing agent in PVA films by increasing molecular mobility, lowering the glass transition temperature (Tg), and promoting thermally induced deformation. The concentration-dependent increase in the diameter of the inhibition zone of essential-oil-added films showed that their antibacterial efficacy increased as the S. aromaticum essential oil content increased (0.5%, 0.75%, and 1.0%). Additionally, molecular docking was performed to examine interactions between selected virulence proteins of K. pneumoniae and the main components of clove essential oil. As a result, S. aromaticum essential oil conferred antibacterial properties to the polyvinyl alcohol films without significantly altering their transparency and thermal properties. Full article

Foaming technology can effectively reduce the viscosity of polymer-modified asphalt and significantly decrease energy consumption during pavement construction, making it an effective approach for achieving low-carbon pavement construction and maintenance. However, mechanically foamed asphalt relies on specialized equipment and requires strict parameter control. Although water-based foaming methods using zeolites or ethanol can alleviate these issues to some extent, they still present disadvantages such as significant variability in foaming performance and potential risks during transportation and construction. Therefore, this study investigates the feasibility of using crystalline hydrates with high water of crystallization for micro-foamed asphalt. Three types of micro-foamed SBS-modified asphalt (MFPA) were prepared using hydrates with different contents of water of crystallization. Physical property tests, foaming characteristic parameters, viscosity–temperature analysis, Fourier transform infrared spectroscopy (FTIR), adhesion tensile tests, scanning electron microscopy (SEM), and fluorescence microscopy were conducted to evaluate their effects on the physical and chemical properties, viscosity reduction performance, adhesion, and compatibility of SBS-modified asphalt. Furthermore, dynamic shear rheometer (DSR) tests, bending beam rheometer (BBR) tests, fatigue life modeling, and morphological analysis were employed to investigate the rheological properties, fatigue life, and bubble evolution behavior of the MFPA system. The results indicate that utilizing the thermal decomposition characteristics of crystalline hydrates with high water of crystallization (Na₂SO₄·10H₂O, Na₂HPO₄·12H₂O, and Na₂CO₃·10H₂O) to release H₂O and CO₂ in SBS-modified asphalt for micro-foaming is a short-term reversible physical viscosity reduction process. The maximum expansion ratio (ERmax) of MFPA reaches 8–10, the half-life (HL) remains stable at approximately 180 s, and the foaming index (FI) peak is about 1160. The construction temperature can be reduced by 10–15%, and the viscosity reduction effect remains stable within 60 min. Compared with unfoamed SBS-modified asphalt, the compatibility, rutting resistance, and fatigue life of MFPA increase by approximately 65%, 32%, and 30%, respectively, while the low-temperature performance decreases by 18%. Under the same short-term and long-term aging conditions, MFPA exhibits better aging resistance. Specifically, its rutting resistance increases by 37%, and fatigue resistance improves by 30% compared with aged SBS-modified asphalt, while the low-temperature performance remains essentially unchanged. Full article

This study evaluates the effectiveness of laser cleaning techniques for the non-contact removal of unwanted deposits from the surface of contemporary urban mural paintings. Two sets of mock-up samples, painted with popular graffiti spray paints on lime-based plaster, and artificially contaminated, were subjected to various cleaning procedures using Nd:YAG lasers operated in Q-switched (QS), long Q-switched (LQS) or short free-running mode (SFR). A multi-analytical approach—including X-ray fluorescence spectroscopy (XRF), Fourier-transform infrared spectroscopy (FTIR), colorimetry, and hyperspectral imaging (HSI)—was used to identify pigments and binders, and to evaluate cleaning efficiency and pigment preservation. XRF and FTIR were useful in understanding the composition of the sprays, while colorimetric ΔE values quantified cleaning efficiency and potential damage, and hyperspectral reflectance and LSU (linear spectral unmixing) abundance maps provided spatial distribution insights into contaminant removal and pigment preservation. The results demonstrate that laser cleaning effectiveness and selectivity are strongly dependent on the operational regime and fluence. In particular, long Q-switched laser irradiation at moderate fluence levels achieved effective contaminant removal with minimal chromatic and chemical alteration of the original paint layers. These findings support the development of tailored, sustainable, and non-contact laser cleaning protocols for the conservation of contemporary urban murals and contribute to the establishment of objective, multi-parameter criteria for evaluating cleaning outcomes in street art conservation. Full article

The changes in functional groups during in situ co-pyrolysis of tar-rich coal with wheat straw were systematically examined using synchrotron diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) coupled with thermogravimetric analysis (TGA). Dynamic changes in C=C, C-O, and C-O-C groups were monitored and assessed across 50–500 °C, complemented by thermogravimetric analysis to assess synergistic effects. It revealed that co-pyrolysis significantly alters the thermal cracking pathways of oxygenated structures, reducing the overall onset temperature by approximately 150 °C. Specifically, instead of maintaining thermal stability, co-pyrolysis promoted early structural aromatization and advanced the C=O decomposition onset by 50 °C compared to coal, achieving a remarkable functional group cleavage rate of 47%. Additionally, the C=C formation temperature was advanced by 150 °C. Furthermore, co-pyrolysis effectively suppressed the secondary structural transformations observed in biomass by limiting the relative accumulation of C–O–C structures to merely a 5% increase, compared to a 52% surge in wheat straw. Interestingly, while DRIFTS confirms facilitated localized bond cleavage and deoxygenation, TGA reveals a macroscopic negative synergy regarding overall weight loss. These findings provide profound insights into the complex radical interactions during co-conversion, offering a crucial theoretical basis for optimizing coal–biomass co-pyrolysis technologies. Full article

Harmonics and interharmonics have a significant impact on the safe operation of power systems, and accurately identifying interharmonics in power systems is the basis of harmonic suppression. The accuracy with which interharmonic components in power systems are detected is easily affected by mode aliasing and noise; to address this issue, a method of detecting them based on an adjusted Fourier-based synchrosqueezing transform (AFSST) and the three-point symmetric difference energy operator (DEO3S) is proposed. First, in order to reduce the influence of endpoint effects on detection accuracy, an improved waveform feature-matching extension method is utilized to reduce endpoint effects generated during the FSST decomposition process. Then, because it is difficult to adaptively determine the number of ridges in the FSST decomposition process, the energy difference and normalized cross-correlation coefficient are utilized as the criterion for determining the number of modal decompositions in the FSST, thereby improving the accuracy of the ridge number. Finally, using AFSST, the harmonic/interharmonic signals are decomposed into a set of intrinsic mode functions (IMFs). The instantaneous frequency and amplitude of each component are extracted using DEO3S, enabling the accurate detection of harmonics and interharmonics in the power system. Experimental analysis was conducted using simulation data, arc furnace experimental system data, and hardware experimental platform data. The results showed that the proposed method can accurately detect harmonic/interharmonic parameters under different levels of noise interference. Compared with the FSST, EMD, EEMD, and CEEMDAN methods, the amplitude detection accuracy of the proposed method is improved by 0.21%, 0.78%, 0.64%, and 0.75%, respectively, and the amplitude detection accuracy is improved by 1.39%, 3.31%, 2.04%, and 3.14%, respectively. Full article

Large amounts of binder system waste are produced upon the recovery of energetic components in scrapped hydroxyl-terminated polybutadiene (HTPB) propellant. This study investigated the biodegradability of the binder system waste using a microbial enrichment solution as the biodegradation medium. We measured the binder system weight loss and performed Fourier-transform infrared (FT-IR), thermogravimetric (TG), and scanning electron microscopy (SEM) analyses of the binder system after 60 days of biodegradation. The results show the binder system film weight decreased by approximately 43% and stabilized after 50 days. The FT-IR analysis shows a reduction in C=O and C-O bond signals, whereas N-H, C-N, and C=C bond signals remain nearly unchanged. The TG analysis shows that the difference between the DOA weight in the initial film and that of the thermal decomposition was almost equal to the weight loss of the binder system film after biodegradation. The SEM analysis shows irregular pits on the film. The binder system has a certain biodegradability, which is mainly caused by its plasticizer component, i.e., DOA. HTPB-based polyurethane, the other major component, is difficult to degrade by microorganisms. As such, the binder system was pretreated with sodium methoxide-methanol solution as a depolymerization reagent, and the pretreated product yielded higher biodegradability. Full article

Urban geophysical exploration faces significant hurdles due to strong electromagnetic interference and limited operational space, which restrict the efficiency and depth of traditional Electrical Resistivity Tomography (ERT). To overcome these limitations, this paper presents a novel ERT measurement and control system based on the Frequency Division Multiplexing (FDM) principle. Unlike conventional time-domain methods, this instrument synchronously transmits three independent AC signals at distinct frequencies. The acquisition station utilizes Fast Fourier Transform (FFT) to isolate specific frequency responses, enabling the simultaneous retrieval of apparent resistivity data for three different electrode spacings from a single transmission. The system architecture integrates low-power STM32 microcontrollers with an Android-based control terminal via Bluetooth, Wi-Fi, and NB-IoT technologies. This wireless design supports real-time current monitoring and cloud-based data synchronization. Experimental results demonstrate that the FDM operating mode significantly enhances data acquisition efficiency and anti-interference capability through frequency-domain separation. Controlled indoor and preliminary field tests indicate that FDM mode substantially improves acquisition efficiency through concurrent multi-channel measurement while effectively resolving target signals from noise. This study demonstrates the system’s technical feasibility and provides a practical foundation for future geophysical detection in time-constrained urban environments. Full article

The valorization of agro-industrial byproducts as sources of functional polysaccharides is a promising strategy for developing sustainable materials. In this study, cellulose was extracted and purified from rice husk and apple pomace through sequential alkaline and bleaching treatments. Then it was chemically modified via TEMPO-mediated oxidation to obtain cellulose nanofibers (TOCNFs) with cellulose yields ranging from 23.8 to 32.4% for rice husk and 9.3–13.8% for apple pomace. Owing to its higher recovery and structural regularity, rice husk was selected for surface modification with 3-aminopropyltriethoxysilane (APTES). The resulting TOCNFs exhibited an average width of 8 nm and a carboxyl content of 0.48 mmol g⁻¹. Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and nitrogen determination (1.72 mg g⁻¹) confirmed the presence of aminosilane functionalities. APTES-modified TOCNFs were incorporated as active components to develop hybrid poly(vinyl acetate) (PVA) adhesives synthesized via in situ heterogeneous water-based polymerization. The influence of TOCNF surface chemistry and sodium dodecyl sulfate (SDS) on latex particle size, rheological behavior, and adhesive performance was systematically investigated. Latex particle size increased from 193 nm (PVA-SDS) to 625 nm with TOCNF-APTES and decreased to 247 nm upon SDS addition. Rheological analysis revealed pronounced shear-thinning behavior associated with the formation of percolated nanofibrillar networks, with low-shear viscosity increasing up to 477 Pa·s for TOCNF–APTES and decreasing to 370 Pa·s with SDS. Lap-shear testing (ASTM D905) showed substantial improvements in adhesive strength, reaching up to 250 kPa compared to PVA-SDS. These results demonstrate that surface-modified CNFs act not only as mechanical reinforcements but also as interfacially active components governing polymerization behavior, rheology, and adhesive performance. This exploratory study provides a proof-of-concept for the development of sustainable wood adhesives from agro-industrial byproducts. Full article

Cold recycled asphalt mixtures incorporate a high amount of reclaimed asphalt pavement (RAP), which offers more economic and environmental advantages than hot recycling techniques. Nevertheless, the presence of aged RAP binder frequently leads to reduced low-temperature performance and uncertainty in mechanical response. The influence of slack wax on full-depth reclamation (FDR) mixtures with bitumen emulsion is assessed in this study using a dual-scale approach. The approach integrates both chemical and rheological binder-scale characterization with mixture-scale mechanical performance with variability assessment. At the binder scale, the binder beam rheometer (BBR), dynamic shear rheometer (DSR), and Fourier transform spectroscopy (FTIR) indicated that the addition of 10% recycling agent improved the low-temperature properties. The improvement at lower temperatures shifted the BBR temperature from −23 °C to −30 °C, which ultimately resulted in a less negative ΔT_c, from −0.7 °C to −0.3 °C, and moderately improved high-temperature stiffness. Moreover, the FTIR analysis indicated a reduction in oxidation-related chemical markers, as evidenced by the reduced carbonyl and sulfoxide indices. At the mixture scale, complex modulus shows a systematic decrease in stiffness, particularly at lower temperatures of −25 °C and −15 °C, and a reduced phase angle, suggesting higher elastic dominance. The reduction is observed at all temperatures and frequencies. Rutting resistance of both formulations remains below 3% after 30,000 cycles. The complex modulus coefficient of variability was found to be 8–12%, comparable to that of hot mix asphalt. In conclusion, the findings suggest that the recycling agent provides a controlled restoration of viscoelastic properties in cold recycled mixtures without compromising structural integrity. This underscores the significance of multi-scale evaluation and variability assessment when characterizing high RAP recycling agents under the studied materials and dosage. Full article

The primary objective of this study is to investigate the effect and mechanism of replacing limestone powder with red mud as a filler on asphalt aging resistance. The microstructure and porosity characteristics of limestone powder, Bayer process red mud, and sintered red mud were analyzed. Asphalt mastics were then prepared using these fillers. The effect of red mud on the aging resistance of asphalt was evaluated by comparing the conventional physical properties, rheological behavior, and functional groups of the asphalt mastics before and after aging. Fourier transform infrared spectroscopy (FTIR), gel permeation chromatography (GPC), and ultraviolet-visible spectroscopy (UV-Vis) were further employed to elucidate the underlying anti-aging mechanisms. The results indicate that the asphalt mastic containing 4% sintered red mud exhibits the strongest resistance to both thermo-oxidative and UV aging. It shows the lowest increments in softening point, viscosity aging index, and complex modulus aging index, with performance comparable to a commercial anti-aging agent. FTIR and GPC analyses reveal that sintered red mud selectively adsorbs light asphalt components, thereby inhibiting their conversion into heavier fractions during thermo-oxidative aging. UV-vis analysis demonstrates that sintered red mud provides effective UV shielding within the asphalt mastic, substantially mitigating UV-induced damage. In summary, the incorporation of 4% sintered red mud can significantly delay both thermo-oxidative and UV aging processes in asphalt mastics, thereby effectively enhancing the aging resistance of asphalt pavement. Full article

Sustainable alternatives to synthetic polymer-based sanitary napkins are essential to reduce the environmental impact and health concerns. This study presents a method for using water hyacinth (Eichhornia crassipes), an invasive aquatic weed, as biomass to produce biodegradable absorbent material for sanitary pads. Water hyacinth fibers were treated with an alkaline solution and incorporated into the absorbent core. Morphological, chemical, structural, functional, microbiological, and biodegradability evaluations were then conducted systematically. Scanning electron microscopy showed that non-cellulosic components were successfully removed, producing a rougher surface topology and enhanced fiber interactions. Fourier-transform infrared spectroscopy confirmed structural changes in cellulose after treatment. Additionally, X-ray diffraction showed that the crystallinity index increased from 53.21% in untreated fibers to 62.56% in treated fibers, indicating improved order and stability. The developed absorbent sanitary pad showed rapid fluid uptake, absorbing 10 mL within three seconds while maintaining a skin-compatible neutral pH of 6.87, as specified in Indian Standard IS 5405:1980. Microbial contamination remained low, with a total bacterial count of 360 CFU/g, no yeast or mold at ≤1 CFU/g, and no presence of Staphylococcus aureus. Soil burial tests showed 70% biodegradability at 40 days and approximately 95% at 60 days, indicating high biodegradability. These findings demonstrate the potential of water hyacinth as an inexpensive and environmentally friendly material for manufacturing hygienic sanitary pads, highlighting the sustainability benefits of valorizing invasive biomass and reducing reliance on synthetic polymers. Full article

Liquid sulfur exhibits the famous $\lambda$-transition at T = 432 K, changing from a liquid mainly consisting of eight-membered rings into a liquid with chains of different lengths. This transition is accompanied by an increase in viscosity that reaches four orders of magnitude. We present a neutron-scattering study conducted throughout the transition to elucidate the slow relaxation dynamics. The data are analyzed within the frequency domain and, after Fourier transformation, in the time domain as well. The relaxation dynamics between 1 ps and 140 ps deviate strongly from simple exponential decay and can be accurately described as stretched exponential decay. The relaxation times demonstrate a change to faster dynamics above the transition at a wave vector corresponding to nearest-neighbor distances. At smaller wave vectors, however, and hence greater length scales, the relaxation times increase with an increasing temperature, evidencing a significant change in dynamics. The Q-dependence of the relaxation rate above the $\lambda$-transition agrees with predictions for polymer melt dynamics. The relaxation dynamics at these length scales are dominated by chain-like structures, and the observed polymer-like dynamics might be the microscopic origin of the increase in viscosity. Full article

Zero-valent iron (Fe(0)) nanoparticles have a wide range of applications, including catalysis, energy storage, and even reported roles in human neurochemistry. This study demonstrated that [Fe₃(CO)₁₂] dissolves in N,N-Dimethylformamide (DMF) within a minute to resolve the dissolution problem of this complex. Dodecylamine (DDA) was used to produce DDA-coated Fe(0) at 383 K in 30 s with a microwave reactor. The powder X-ray diffraction (PXRD) of the Fe(0) profile indicated a pure-phase face-centred cubic (FCC) structure with Fm$\overline{3}$m space group. Varying the synthesis time from 30 s to 5 min did not significantly affect the unit cell parameters (3.5276 (±0.0001) and 3.5391 (±0.0001) Å). Microwave use yielded well-dispersed, pure Fe(0) nanoparticles, and the particle size, shape, elemental analysis, and surface oxidation of the Fe(0) nanoparticles were studied using scanning electron microscopy and dispersive X-ray spectroscopy (SEM/EDX). Annular Dark-Field Scanning Transmission Electron Microscopy (ADF-STEM) and Fourier-transform infrared (FT-IR) spectroscopy confirmed the surface coating of Fe(0) nanoparticles with DDA. Thermogravimetric analysis (TGA) was used to demonstrate the surface adsorption of DDA on Fe(0) nanoparticles. In addition, STEM showed that the average nanoparticle size under the stated synthesis conditions was 25.7 nm. This comparatively straightforward procedure offers advantages over existing practical approaches to the synthesis of Fe(0) nanoparticles, including safety, speed and reaction control. Full article