Search Results (13,782)

Biomass thermochemical conversion-derived hydrochar has been increasingly recognized as a functional resource for environmental remediation, but knowledge about the effect of the carbonization conditions on the surface chemistry and binding behaviour of hydrochar is still limited. In this study, hydrochar from two different processing pathways, pressure reactor carbonization (P-RC) and microwave-assisted carbonization (M-RC), is compared to understand the mechanisms of contaminant interaction and the changes in structure that occur during the carbonization processing. P-RC was synthesized at the hydrothermal temperatures (180, 220, and 250 °C) for 2 and 5 h, while M-RC was synthesized at microwave irradiation for 30 min and 1 h. TGA, SEM–EDS, FTIR, and XRD were used for comprehensive characterization, which revealed systematic differences in functional group distribution, mineral phases, and microstructural development between the two carbonization methods and at different carbonization temperatures. The increase in P-RC temperature led to greater aromatic condensation, thermal stability, and mineral reorganization, while M-RC maintained a higher percentage of oxygenated functionality and a more heterogeneous surface morphology. Batch adsorption experiments indicated that the M-RC hydrochar had a faster adsorption rate, attributed to its greater number of reactive oxygenated functionalities, whereas the P-RC hydrochar produced at higher temperatures exhibited a more even distribution of adsorption sites and stronger mineral-assisted interactions. The kinetics and isotherm modeling also showed different interaction pathways: for M-RC, surface complexation on heterogeneous sites was favored, whereas for P-RC, a more monolayer-like adsorption was observed. These results collectively show how the method and temperature of carbonization affect reactivity and support the establishment of mechanistic relationships crucial to maximizing the utility of hydrochar as a functional material for environmental remediation. Full article

Developing advanced bioinspired photoprotective barrier from marine resources represents a critical frontier of bioprocessing. This study established a rational design and implementation of effective photoprotective surface-coating eumelanin from ink of an Indian squid (Uroteuthis duvaucelii). The Central Composite Design was developed to optimize extraction and functionalization parameters of eumelanin on quartz substrates, strategically developing the matrix for peak optical attenuation within the potential Far-UVC window (220 nm). Translational photoprotective efficacy of the surface, as well as finished eumelanin on quartz surface, was validated by subjecting them to a challenging macro-level biological assay using a hospital-grade 254 nm ultraviolet germicidal source (125 µWcm⁻²). Quantitative physical dosimetry established that the squid eumelanin coating (A254 = 1.00) reduced internal transmittance to approximately 10%, successfully dampening the incident fluence from 0.225 J cm⁻² down to a heavily attenuated 0.0225 J cm⁻² at the biological sample plane. While unshielded control indicator microbial strains suffered complete lethal inactivation, the eumelanin barrier maintained exceptional cell viability, yielding biological shielding efficiencies of 98% for Bacillus subtilis, 96% for Staphylococcus aureus, and 92% for Escherichia coli. Characteristic features from FE-SEM, FTIR, and XRD analysis established that this superior photoprotective property is governed by the extensively conjugated, π-π-stacked indolic architecture possessing a characteristic 3.4 Å interlayer d-spacing, which facilitates rapid, non-radiative energy dissipation. This work establishes an effective framework for translating squid biomass into high-value, transparent optical barriers, providing a potential sustainable alternative to synthetic ultraviolet absorbers. Full article

In the present work, four grades of austenitic stainless steels, namely AISI 321, AISI 316Ti, AISI 309, and AISI 310S, are investigated in terms of electrochemical hydrogenation effect on their room-temperature impact toughness. All the materials were studied in their as-received (AR), i.e., industrially manufactured, material condition. LOM and SEM microstructural analyses combined with phase XRD and EBSD phase analyses revealed in all steels the polygonal-grain austenitic matrix and varying minor amounts of elongated δ-ferrite grains. Moreover, the metastable AISI 321 and AISI 316Ti steels exhibited noticeable occurrence (16% and 10%, respectively) of the BCC-structured phases (i.e., the strain-induced α′-martensite and non-equilibrium δ-ferrite) and little occurrence of primary TiN nitrides (below 1%). The AISI 321 and AISI 316Ti steels exhibited average amounts of 2.95% and 6.32% of δ-ferrite, respectively. The stable AISI 309 steel exhibited the occurrence of intergranular (Cr,Fe)₂₃(C,N)₆ precipitates (below 3%), indicative of prolonged (slow) cooling from the warm working temperature during the material manufacturing. The individual steel grades exhibited variable values of hardness and impact toughness depending strongly on their solid solution alloying and the amounts of individual minor phases in their microstructures. The AISI 316Ti steel exhibited the highest average hardness (273 HV) and lowest impact toughness (160 J/cm²) due to Mo-alloying and having the highest amount of δ-ferrite. The AISI 310S steel showed the highest impact toughness (210 J/cm²) and the second highest hardness (245 HV) thanks to having the most stable austenitic microstructure with the highest Ni- and Cr-alloying. The AISI 321 and AISI 309 steels show similarly low hardness (195 HV vs. 196 HV) and medium values of impact toughness (202 J/cm² vs. 193 J/cm²). More importantly, all the steels under investigation exhibited detectable hydrogen-induced toughening effects, indicated by the negative HEI values. The metastable steels showed the lowest toughening effects (HEI: −2.0% and −3.8% for AISI 321 and AISI 316Ti, respectively), likely due to the adverse effect of α′-martensite. In contrast, the stable steels exhibited much higher toughening (HEI: −5.2% and −7.6% for AISI 309 and AISI 310S, respectively). Microstructural observations indicated that such toughening behavior might be related to the hydrogen-enhanced deformation banding and hydrogen-enhanced deformation twinning mechanisms, dividing the grains into smaller deformation zones, increasing the overall dissipation of deformation energy and consequently the materials’ impact toughness. Full article

With increasing global concerns about industrial wastewater treatment and the need for sustainable practices, this study explores the potential of softwood sawdust as an eco-friendly, cost-effective adsorbent for removing heavy metal ions, specifically zinc (Zn²⁺) and lead (Pb²⁺), from synthetic model solutions. Factors affecting adsorption include adsorbent particle size, pH, adsorbent dosage, and contact time. A remarkable removal efficiency of 98.2% for Zn²⁺ and 98.1% for Pb²⁺ under optimal adsorption conditions of −106 µm average particle size at 8 pH and 0.3 g of adsorbent dosage using 50 (mg/L) initial concentrations for 60 min at ambient temperature. Characterization of the adsorbent used by XRD, FTIR, SEM, and BET analysis confirmed the structural integrity and surface properties of wood sawdust. It is clear that there is a gradual decline in adsorption capacity over multiple reuse cycles due to the depletion of active functional groups. The results confirm wood sawdust’s effectiveness as a locally available, low-cost, and biodegradable option for treating wastewater, eliminating metal ions, supporting environmental conservation, and aligning with sustainability goals. Full article

Cement slurry is a staple grouting agent, yet its properties can weaken when exposed to heat. Studying grouting materials for use in high-temperature tunnels is therefore a matter of considerable importance. To enhance the applicability of cement-based slurry in high-temperature tunnels, multi-walled carbon nanotubes (MWCNTs), polycarboxylate ether superplasticizer (PCE), and hydroxypropyl methylcellulose (HPMC) were added to improve their performance at elevated temperatures. Various experimental methods were employed to investigate the properties of the modified slurry at different temperatures, including flowability, setting time, compressive strength, and dynamic water retention ratio. Additionally, X-ray diffraction (XRD), thermogravimetric analysis (TG), and scanning electron microscopy (SEM) were used to study the effects of temperature on hardened slurry. Experimental results indicate that the optimal MWCNTs content is 0.32%. At this content, the compressive strength of the hardened slurry after 28 days of curing at 80 °C increases by approximately 20%, reaching 26.4 MPa. PCE improves the fluidity of the slurry, while HPMC enhances its water dynamic water retention ratio. The optimal proportion was found to be 0.3% PCE and 0.2% HPMC. At this ratio, the fluidity of the slurry increased by about 8%, reaching approximately 17.7 cm; the dynamic water retention ratios of 0.8 m/s and 1.0 m/s improved by approximately 22% and 38%, respectively, achieving 35.8% and 18.1%. Furthermore, multi-walled carbon nanotubes significantly enhance the compressive strength of the hardened slurry primarily by suppressing the formation of ettringite during the later stages of hydration, as well as by providing nucleation sites, encapsulating hydration products, and bridging hydration product clusters within the microstructure. This investigation lays a theoretical groundwork for formulating and choosing grouting materials suited to high-temperature tunnel environments. Full article

Chlorophyll, a natural photosynthetic pigment, is gaining interest for its sustainable and eco-friendly applications in renewable energy, particularly as a photosensitizer in dye-sensitized solar cells (DSSCs). This study investigates the feasibility of chlorophyll extracted from Moringa oleifera as a natural photosensitizer in DSSCs, building on our previous work demonstrating its high chlorophyll content and long-term stability. Chlorophyll was extracted using acetone under optimal conditions (45 °C, 60 min) and applied in DSSCs comprising a TiO₂ photoanode, iodide/triiodide electrolyte, and platinum counter electrode. The TiO₂ photoanode was characterised using UV-Vis spectroscopy, FE-SEM, XRD, and Raman spectroscopy, confirming the presence of pure anatase phase TiO₂ with uniform spherical nanoparticle morphology. The fabricated DSSCs achieved a short-circuit current density of 0.197 mA cm⁻², an open-circuit voltage of 0.44 V, a fill factor of 32%, and a photoconversion efficiency (PCE) of 0.027%. While this performance is lower than the highest reported chlorophyll-based DSSC efficiency (4.6%), the results demonstrate that M. oleifera is a viable and sustainable source of chlorophyll for DSSC applications. The findings highlight the importance of dye–semiconductor interactions and suggest that further optimisation through co-sensitization, TiO₂ surface modification, and improved dye anchoring could enhance device performance. Full article

ZBLAN (ZrF₄-BaF₂-LaF₃-AlF₃-NaF) fluoride glass is a promising infrared optical fiber material because of its wide transmission window and low theoretical attenuation; however, unwanted crystallization during thermal processing can introduce scattering centers and degrade optical performance. Previous studies have mainly focused on temperature effects and microgravity-based crystallization suppression, while the role of mechanical vibration remains insufficiently understood. This study addresses this gap by investigating how controlled mechanical vibration influences crystallization onset, morphology, and structural evolution in ZBLAN glass during short-duration thermal treatment. ZBLAN samples were treated at selected temperatures with and without vibration using a custom heating–vibration apparatus and characterized by optical microscopy, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), atomic force microscopy (AFM), and X-ray diffraction (XRD). Temperature-only treatment produced a gradual transition from transparent amorphous glass to crystallized structures with increasing temperature. Vibration-assisted treatment altered crystallization behavior, producing distinct needle-like, bow-tie, and feather-like morphologies depending on temperature and vibration intensity. AFM confirmed a significant increase in surface roughness, while XRD verified structural evolution from amorphous to highly crystallized states. At higher vibration levels, irregular crystallization suggested that excessive sample movement may reduce thermal contact and change the effective heating condition. These findings demonstrate that mechanical vibration is a critical and controllable processing variable in ZBLAN fabrication and should be carefully managed to suppress unwanted crystallization in both terrestrial and space-based fiber manufacturing. Full article

Wastewater containing heavy metals and dyes poses serious environmental risks. This study developed a multifunctional composite by coating polyurethane foam (PUF) with milled activated carbon (mAC) and a zirconium-based metal–organic framework (Zr-MOF) for the simultaneous removal of hexavalent chromium (Cr(VI)) and Congo red (CR). The composite was synthesized using a hydrothermal method to grow Zr-MOF on the surface. The SEM analysis confirmed the successful incorporation of mAC and surface modification with Zr-MOF, which resulted in increased surface roughness and porous morphology. XRD and FTIR confirmed the presence of organic ligands connected to the metal structure and the functional groups of each component in composite materials. The optimum conditions for Zr-MOF/mAC/PUF adsorption (nearly 100% removal) in the binary Cr(VI)/CR solution (50 mg/L each) were 25 °C, pH 9, and 150 rpm for 24 h. The Zr-MOF/mAC/PUF was hydrophilic with a swelling ratio of 2.64 g/g. The thermodynamic investigation of Zr-MOF/mAC/PUF resulted in 141.6218 kJ/mol for Cr(VI) and 166.111 kJ/mol for CR of ΔH° (rapid adsorption), negative ΔG° (spontaneous adsorption), a high positive value of ΔS° (disorder structure) and low activation energy (approximately 2.5 to 2.8 kJ/mol). After analyzing the isotherm and reaction kinetics, the possible mechanism could be endothermic physicochemical adsorption and pseudo-second-order kinetic behavior, with electrostatic attraction and diffusion control. The study of 6-times-reused Zr-MOF/mAC/PUF adsorption identified as a decrease of 7.55 percentage point without changing notable morphology and functional groups, based on SEM and FTIR. Full article

Oxide systems with the nominal composition LaCaCuVMnO_7.5 and composites modified with the YBa₂Cu₃O_x phase were synthesized by the solid-state reaction method. The phase composition and structural features were systematically investigated by X-ray diffraction (XRD), Rietveld refinement, and scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM–EDX). The parent oxide was found to form a two-phase system, consisting of an orthorhombic perovskite-like phase and a cubic manganite–vanadate phase, whereas the introduction of 10 wt.% YBa₂Cu₃O_x resulted in the formation of a three-phase composite containing an additional cuprate phase. Thermophysical investigations in the 298–673 K range revealed λ-type-like anomalies in the heat capacity, which may be associated with possible structural or interphase transformations in the investigated oxide systems. The incorporation of YBa₂Cu₃O_x significantly modified the temperature dependence of heat capacity and increased its values over both low- and high-temperature regions. Electrophysical measurements in the 293–483 K range confirmed the semiconducting nature of conductivity, while the addition of YBa₂Cu₃O_x reduced electrical resistance and enhanced dielectric permittivity. These findings demonstrate that YBa₂Cu₃O_x modification provides an effective route for tuning the thermophysical and electrophysical properties of LaCaCuVMnO_7.5-based oxide systems, suggesting their potential as promising candidates for multifunctional oxide materials with possible electronic and sensor-related applications. Full article

Despite the advantages of powder bed fusion–laser beam (PBF-LB), Ti6Al4V components often exhibit high yield strength but limited ductility, which restricts their use in critical structural applications. This study aims to identify the most effective heat treatment to optimize the strength–ductility balance in Ti6Al4V parts produced by PBF-LB and to establish direct correlations between microstructural states, mechanical properties and corrosion behavior. Two distinct post-processing heat treatments were applied, specifically, the first at 500 °C for 5 h and the second at 800 °C for 2 h, both followed by air cooling. The microstructure was characterized using optical microscopy (OM), scanning electron microscopy (SEM), and X-ray diffraction (XRD). Mechanical behavior was assessed through Vickers microhardness testing and tensile testing, while corrosion resistance was evaluated via electrochemical measurements. Residual stress profiles were determined using the hole-drilling strain gauge method, in both as-built and heat-treated conditions. The as-built samples displayed a fully martensitic α′ structure with columnar grains aligned parallel to the laser scanning direction, resulting from rapid solidification. Heat treatment at 500 °C caused only partial decomposition of acicular martensite into substructures without altering its acicular morphology, leading to a strengthening effect alongside a reduction in ductility. Conversely, heat treatment at 800 °C offered the most balanced combination of strength and ductility among the conditions studied, albeit with a moderate reduction in corrosion resistance. Full article

The applied design of recycled aggregate concrete (RAC) with supplementary cementitious materials (SCMs) requires reliable estimation of 28-day flexural strength (FS28) before trial batching. This is challenging because RAC–SCM mixtures involve nonlinear interactions among binder chemistry, aggregate replacement, water-to-binder ratio, and admixture dosage. However, most predictive models focus on compressive strength or sustainability optimization, while fewer address FS28 using chemically informed descriptors and independent validation. This study developed and externally validated an XGBoost framework for FS28 prediction. The methodology combined binder characterization by XRF, XRD, SEM, and particle-size analysis; reactivity descriptors; database development; modeling; and experimental validation. A database of 397 mixtures from 22 sources was refined to 382 observations for training and testing, and the model was validated with 58 RAC–SCM mixtures and 174 prismatic specimens tested according to ASTM C78/C78M-22. XGBoost achieved R² values of 91.61%, 80.75%, and 77.62% for training, testing, and validation, with RMSE values of 0.559, 0.835, and 0.364 MPa. Compared with the best alternative models, XGBoost reduced RMSE by 8.6% in testing and 9.5% in validation. Interpretability analysis identified binder reactivity, water-to-binder ratio, aggregate composition, cement content, SCM replacement, and superplasticizer dosage as key factors. Full article

Sargassum biomass has attracted increasing attention due to its massive accumulation along the Mexican Caribbean coast (Riviera Maya) and its potential role in carbon cycling. Although previous studies have reported calcium carbonate formation associated with Sargassum, the crystallographic nature of these biomineralized phases and the possible incorporation of Mg into the carbonate lattice remain poorly understood. In this study, carbonate phases associated with Sargassum collected from the Mexican Caribbean were investigated using X-ray diffraction (XRD), Rietveld refinement, Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy coupled with energy-dispersive spectroscopy (SEM-EDS), and transmission electron microscopy (TEM). Structural, morphological, and compositional analyses consistently revealed calcite as the dominant carbonate phase, exhibiting lattice modifications associated with Mg incorporation. Rietveld refinement identified crystallographic changes consistent with Mg substitution within the calcite lattice, while complementary characterization confirmed Mg-bearing carbonate domains and local structural distortions characteristic of high-Mg calcite (HMC). The combined results provide strong evidence for the formation of HMC associated with Sargassum, demonstrating that Mg incorporation occurs within the carbonate structures of a non-calcifying brown macroalga, a process previously reported predominantly in calcifying organisms and calcareous algae. These findings expand the current understanding of biomineralization pathways in marine ecosystems and suggest that Sargassum can promote the transformation of dissolved inorganic carbon into carbonate minerals. The occurrence of HMC highlights the potential role of Sargassum as a natural bioremediator and a contributor to transient carbon fixation through carbonate formation, providing new insights into the role of brown macroalgae in carbonate production and carbon cycling. Full article

Hydrated lime is widely incorporated into cement-based mortars to improve workability and fresh-state properties; however, its influence on hydration products and mechanical performance remains insufficiently understood. This study investigates the effect of hydrated lime content on the mechanical behavior and microstructural development of cement-based mortars after 28 days of curing. Eight mortar formulations, ranging from lime-free (1:0:6) to lime-rich (1:5:6) mixtures, including intermediate and modified proportions, were evaluated through compressive strength, flexural tensile strength, and consistency tests. The microstructural evolution was investigated using complementary techniques, including X-ray fluorescence (XRF), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TG/DSC), and scanning electron microscopy coupled with energy-dispersive spectroscopy (SEM/EDS). Increasing hydrated lime content improved mortar workability but was generally associated with reduced compressive strength under the curing conditions investigated. The combined characterization techniques indicated progressive modifications in the hydration products and phase assemblage, with increased calcium-rich phases, greater evidence of carbonation, and reduced continuity of the hydraulic matrix as the hydrated lime content increased. The observed microstructural changes were qualitatively consistent with the mechanical behavior of the mortars. The conclusions of this study are restricted to the 28-day curing period investigated, and further research is required to evaluate the long-term influence of hydrated lime on carbonation and durability-related properties. These findings contribute to a better understanding of the role of hydrated lime in cement-based mortars and provide experimental evidence for the optimization of mortar formulations. Full article

To support the achievement of the carbon peaking and carbon neutrality goals and promote the resource utilization of industrial solid waste, a ternary solid waste composite cementitious material was prepared by blending ground granulated blast-furnace slag (GGBFS), fly ash (FA), and carbide slag (CS) with cement. The optimal mix ratio was determined through single-factor experiments and response surface methodology. The synergistic hydration mechanism was elucidated using microstructural characterization techniques, including XRD, FTIR, TG-DTG, and SEM. The composite material was then applied to a semirigid base course, and its mechanical properties and durability were systematically evaluated. The results indicate that the optimal levels of FA, GGBFS, and CS investigated in the single-factor experiments are 20–40%, 30–50%, and 2–6%, respectively. The optimal mix ratio of the ternary solid waste composite is 21.0% FA, 36.3% GGBFS, and 5.7% CS. The underlying microstructural mechanism is that carbide slag creates a highly alkaline environment, which activates the pozzolanic activity of GGBFS and fly ash, leading to the formation of hydration products dominated by C-(A)-S-H gel. With increasing curing age, the gel structure evolves from a loose and disordered state to a dense and ordered state, ultimately forming a compact microstructure based on a highly polymerized C-(A)-S-H gel matrix. The 7-day unconfined compressive strength of the stabilized gravel using the solid waste-based composite cementitious material reached 5.93 MPa, and the 28-day drying shrinkage coefficient was reduced by 18.3% compared with that of cement-stabilized gravel. After 18 freeze–thaw cycles, the compressive strength increased by 2.4%, with the pore structure characterized by a “macropores decreasing, micropores increasing” refinement pattern. After 18 wetting–drying cycles, the cumulative strength loss was 11.26%, outperforming cement-stabilized gravel. Combined with SEM observations, these performance improvements are attributed to the densely intertwined hydration products, particularly C-S-H gel, which effectively fill the voids between aggregate particles and significantly enhance the volume stability, freeze–thaw resistance, and wetting–drying durability of the stabilized gravel. The application of this cementitious material in a semirigid base course demonstrates excellent mechanical and durability properties, providing a theoretical basis and technical support for the widespread application of industrial solid waste in road engineering. Full article

In this study, five Fe-rich scoria-based glass compositions were prepared using natural scoria, recycled glass cullet, limestone, and magnesite through the melt-quenching technique at a temperature of 1400 °C for 2 h. The effect of Fe₂O₃ content (2.9–14.5 wt%) on the thermal behavior, crystallization, density, and predicted optical properties of glass was investigated. Differential thermal analysis revealed that increasing Fe₂O₃ content leads to a variation in glass transition (Tg = 632–669 °C) and an increase in softening temperatures (Ts = 711–737 °C), accompanied by an expanded thermal stability window (∆T = Tx − Tg) up to 254 °C, indicating enhanced resistance to crystallization and improved thermal stability. The density measurement showed a non-monotonic variation with composition, due to the combined effect of Fe₂O₃ enrichment and network structural modification. The crystallization behavior of the Fe-rich scoria-based glass (H50) was further studied after heat treatment at 900 °C and at 950 °C using XRD and SEM analysis. The heated samples exhibited the formation of crystalline phases including diopside, gehlenite, wollastonite, maghemite, and anorthite. While SEM observation revealed progressive crystal growth and microstructural densification with increasing heat treatment temperature, indicating the transformation from glass to glass–ceramic. In addition, a semi-empirical optical assessment based on literature-derived models suggested increased absorptance from 97.26% to 98.83% and reduced reflectance with increasing Fe₂O₃ content. However, these optical parameters show theoretical estimates and require experimental validation. These findings demonstrate the potential of Fe-rich scoria-based glasses as thermally stable materials for high-temperature and energy-related applications while using natural and industrial waste sources. Full article