Search Results (6,347)

Spontaneous imbibition modified by surfactants is a key technology for enhancing shale oil recovery. Currently, relevant studies mainly concentrate on marine shale worldwide, while the pore–fluid coupling characteristics of widely distributed medium-TOC terrestrial shale remain poorly understood. Against this background, this paper takes typical Paleogene terrestrial shale as the research object and integrates N₂/CO₂ adsorption and NMR T₂ spectroscopy to jointly characterize multiscale pore structures and dynamic fluid evolution during imbibition. The results show that the shale is dominated by mesopores in terms of pore volume, while micropores provide most of the specific surface area. The zwitterionic surfactant HPSB can greatly reduce oil–water interfacial tension and alter rock wettability, thereby breaking the high capillary resistance of micropores. During imbibition, water invades macropores first, followed by mesopores and micropores, and the entire process exhibits remarkable nonlinear dynamics controlled by multiscale pores. The 0.15% HPSB solution shows the best effect on activating micropores. This study innovatively quantifies the influence of surfactant concentration on fluid migration across different pore scales and reveals the internal mechanism of staged imbibition and micropore lag activation in terrestrial shale. It not only complements the global research system of shale imbibition theory but also offers practical guidance for the optimization of fracturing fluid systems in mesopore-dominated shale oil reservoirs. Full article

High-sensitivity detection of formaldehyde is critically important for environmental protection and public health. Zinc oxide (ZnO) is a widely used core material for chemiresistive gas sensors; however, its conventional low-index facets suffer from a limited number of active sites, creating a bottleneck for further sensitivity enhancement. To overcome this limitation, this study pioneers the application of the highly reactive ZnO $\left[20\overline{2}1\right]$ high-index polar surface for formaldehyde detection. By leveraging its unique stepped atomic configuration and unprecedented density of coordination-unsaturated active sites, we systematically investigate the formaldehyde adsorption behavior and the underlying sensing mechanism using first-principles calculations based on density functional theory (DFT). The pristine ZnO $\left[20\overline{2}1\right]$ surface exhibits intrinsic metallic character. At a coverage of 1 monolayer (ML), the most stable G1 configuration achieves an adsorption energy of −1.54 eV per CH₂O molecule. Within a 2 × 1 supercell, formaldehyde adopts both associative and dissociative adsorption modes. At a lower coverage, formaldehyde forms a stable bidentate structure through dual C–O and Zn–O bonding interactions. Electronic structure analysis reveals significant orbital hybridization and interfacial charge redistribution upon adsorption. Notably, associative adsorption opens a bandgap of 0.04 eV at the Fermi level, inducing a metal-to-semiconductor transition. In contrast, dissociative adsorption results in pronounced n-type doping, thereby elucidating the microscopic origin of the resistivity decrease observed in ZnO-based sensors. Overall, this work highlights the structural advantages of high-index facets and demonstrates for the first time the superior formaldehyde adsorption capability of the ZnO $\left[20\overline{2}1\right]$ facet, providing robust theoretical guidance for the rational design of next-generation, high-performance gas-sensing materials. Full article

The problem of chromium contamination, especially Cr(VI), in acidic wastewater has drawn significant attention, requiring effective and sustainable remediation measures. In this study, tannic-acid/Fe₃O₄-modified corn straw biochar (Fe-TA-CSB) is prepared by a grinding-calcination method to remove Cr(VI). The factors influencing the removal effect of Fe-TA-CSB are investigated through static adsorption experiments. The removal mechanism is explored by combining adsorption kinetics, isothermal adsorption, and thermodynamics, as well as characterization methods. The results show that the removal efficiency of Cr(VI) increases with the increase in pH, contact time (t), and solid–liquid ratio (m/v), but decreases with the increase in initial concentration (C₀). Under optimal conditions of TA/Fe₃O₄ mass ratio = 12.5%, pH = 3.0, m/v = 1.0 g/L, and C₀ = 10 mg/L, the removal efficiency value is 94.02%, which is approximately 81.44% after four adsorption–desorption cycles. The adsorption behavior is fitted well by the Sips isotherm model and Elovich kinetics model, suggesting the adsorption process of heterogeneous monolayer chemisorption. The removal mechanism of Cr(VI) by Fe-TA-CSB involves electrostatic interaction with Cr(VI), reduction in Cr(VI) to Cr(III) through C–O and Fe(II), and complexation of reduced Cr(III) with the introduced Fe–O and phenolic hydroxyl groups. Fe-TA-CSB is an environmentally friendly and renewable adsorbent with good potential for the treatment of acidic wastewater. Full article

Polymer coatings are integral to nearly every modern cardiovascular and endovascular device, including drug-eluting stents (DESs) and drug-coated balloons (DCBs), bioabsorbable vascular scaffolds (BVSs), occluders, grafts, and catheter and guidewire hydrophilic surfaces. Persistent complications, including late stent thrombosis, delayed endothelialization, hypersensitivity, and restenosis, show that coatings actively shape biological responses rather than acting as inert drug carriers. Their surface chemistry, drug release kinetics, and degradation behavior are upstream determinants of blood– and tissue–material responses that govern healing and failure. This review frames coating selection as a structure–property–biological response problem. It surveys the major classes of synthetic polymer coatings and the defining surface and bulk properties. This review also examines how composition and architecture control drug release, and traces the interfacial cascade of protein adsorption, coagulation and complement activation, platelet and leukocyte responses, and neutrophil extracellular trap (NET) formation. These mechanisms are linked to contemporary design strategies that improve hemocompatibility, limit thrombosis, promote endothelial recovery, and tune degradation, and to the standardization and translation gaps that remain. The central message is that polymer coatings are not biologically equivalent. Their surface chemistries and degradation profiles determine the thrombo-inflammatory outcomes. Therefore, coating design should be guided by intended biological response, not drug release alone. Full article

Magnesium–rich environments are frequently encountered in cementitious systems, including the use of high–Mg raw materials in clinker production, cement–clay interfaces relevant to nuclear waste disposal, and exposure of cement–based materials to seawater, where progressive decalcification can substantially alter the structure and durability of calcium aluminosilicate hydrate (C–A–S–H) phases. In this study, density functional theory (DFT) calculations were employed to investigate the combined effects of interlayer and intralayer partial decalcification, Mg²⁺ substitution, and reinforcement with epoxy– and hydroxyl–functionalized reduced graphene oxide (rGO) on the structural stability and elastic properties of alkali charge–balanced C–A–S–H under dry and hydrated conditions. Adsorption–energy calculations reveal thermodynamically favorable interactions between functionalized rGO and silicate hydrate species in the presence of Mg²⁺, with hydroxyl/rGO promoting stronger interfacial stabilization and epoxy/rGO preserving greater graphene lattice integrity. The results demonstrate that Mg²⁺ substitution together with rGO intercalation generally enhances the mechanical response of partially decalcified structures through structural densification and interfacial cohesion. Relative to dry systems, hydration further improves elastic performance, increasing Young’s modulus and bulk modulus by 1–11% and 4–19%, respectively, for interlayer decalcified nanocomposites, while intralayer configurations exhibit stronger but model–dependent enhancements of up to ≈22% and ≈33%. Compared with untreated systems, rGO–treated nan–composites exhibit enhanced stiffness, with Young’s modulus and bulk modulus increasing by up to ≈22% and ≈15%, respectively. Overall, these findings provide atomistic insights into stabilization mechanisms in partially decalcified alkali charge–balanced C–A–S–H systems and identify Mg²⁺–rGO incorporation as a promising strategy for mitigating decalcification–induced degradation in durable low–carbon cementitious nanocomposites. Full article

Phosphorus (P) accumulation in intensively agricultural soils represents a growing environmental concern due to its potential mobilization and contribution to eutrophication. This study investigated the mechanisms controlling P availability and redistribution in agricultural soils from the Elota–Piaxtla Irrigation District (northwestern Mexico) during cropping and non-cropping periods. Soil P fractions were determined using the Hedley sequential extraction method and related to soil physicochemical properties through a correlation analysis. During the cropping period, P in Fe/Al hydroxides dominated (45–67% of total P), indicating strong adsorption and fixation in fine-textured soils. In contrast, the non-cropping period showed a significant increase in organic P in humic substances (up to 55%), suggesting enhanced biological transformation and residue recycling. Labile P fractions decreased from 60% to 44% of total P between sampling periods, while moderately labile fractions increased, indicating seasonal redistribution of P pools. Statistical analysis revealed that P dynamics were primarily governed by mineralogical characteristics and organic matter transformations rather than by individual soil properties. The accumulation of moderately labile and organic P fractions during fallow periods highlights a latent environmental risk, particularly in irrigated systems prone to runoff and erosion. These findings emphasize the need for fraction-based nutrient management strategies that integrate both agronomic efficiency and environmental protection in intensive agricultural soil. Full article

Acid mine drainage (AMD) is enriched with arsenite (As(III)), arsenate (As(V)), and jarosite. While jarosite can immobilize arsenic (As) through adsorption and other mechanisms, it dissolves and transforms into other minerals under near-neutral and reducing conditions via microbial mediation, thereby altering As fate. Fulvic acid (FA), a ubiquitous natural organic matter in the environment, has been proven to exhibit complex interactions with various iron minerals, Fe/S-metabolizing microorganisms, and As. However, the role of FA in the bioreduction and transformation of jarosite, as well as its subsequent impact on As mobility and fate, remains unclear. This study aims to elucidate the regulatory effect of FA on the biodissolution and transformation of jarosite, and the corresponding changes in As speciation. The results showed that FA exerted contrasting effects depending on arsenic speciation. In the As(III) treatments, FA intensified the inhibition of microbial dissimilatory sulfate reduction, suppressed sulfide production, and consequently limited orpiment formation. In contrast, in the As(V) treatments, FA enhanced the association of As(V) with jarosite surfaces, reduced aqueous As stress, and supported the persistence of As-tolerant sulfate-reducing populations. This promoted jarosite transformation toward mackinawite and facilitated As immobilization through orpiment precipitation. This study reveals the critical role of FA in the migration and transformation of As in mining areas, providing novel insights for optimizing AMD remediation strategies such as soil capping. Full article

Sustainable lightweight materials based on renewable resources have attracted increasing attention as alternatives to synthetic materials. However, developing nanocellulose cryogels with adequate structural integrity and efficient retention of phenolic compounds remains challenging, often requiring furanic and dialdehyde-based additives associated with environmental and health concerns. In this context, tannin-containing nanocellulose cryogels were produced using vanillin and hydrogen peroxide as sustainable modification agents. The effects of the additives on the structural, morphological, colorimetric, mechanical, thermal, and leaching properties of the cryogels were investigated. FTIR and colorimetric analyses revealed the presence of phenolics and the effect of hydrogen peroxide. SEM analysis showed that tannin promoted structural densification, whereas peroxide induced fragmentation of the cryogel network and pore reorganization. These changes influenced density and mechanical performance, with nanocellulose-tannin exhibiting the highest compressive strength and elastic modulus. Thermal conductivity values remained within the range reported for highly porous lignocellulosic materials (38.93–43.79 (mW/m·K)). Tannin leaching demonstrated that peroxide significantly improved tannin retention, especially in the system including vanillin which exhibited only 13,61% tannin release. Overall, vanillin and hydrogen peroxide modified the supramolecular organization and functional properties of the cryogels, highlighting their potential as additives in porous materials for thermal insulation and adsorption applications. Full article

This study reports the preparation of a nanocomposite using a black cumin surface as a carbon framework on which zinc oxide-doped manganese ferrite nanoparticles were deposited and grown. A simple precipitation method was used to prepare the nanocomposite. The resulting composite was characterized using various characterization analyses such as FTIR, XRD, EDX, SEM, TEM, and TGA. The composite surface was highly conformed with functional groups, and the nanocomposite was formed due to electrostatic and non-electrostatic interactions between the carbon framework and the nanoparticles. X-ray analysis revealed a crystalline structure with crystal sizes up to 45 nm. Microscopic images revealed the surface morphology, confirming the irregular distribution of particles within the composite. The resulting composite material was used for adsorption application. The composite material was tested for the removal of Congo red dye from water. It was found that under optimal conditions, a dose of 2 g per liter of absorbent removed nearly 100% of dye from a 10 mL volume of 10 mg per liter Congo red solution within 90 min and 7 pH. A monolayer adsorption was confirmed by the isotherm analysis. The monolayer adsorption capacity for the present study was ~13.0 mg per gram. The adsorption kinetics suggested the fitting of pseudo-second order. Based on the findings, it was concluded that the chemical mechanism was responsible for the present adsorption process. The regeneration study demonstrates the stability of current adsorbent up to two cycles only. This nanocomposite is the first of its kind which promotes the creation of nanocomposites in the future by using natural materials and reduces the dependency on activated carbon. Full article

Microplastics (MPs) have emerged as persistent environmental contaminants due to their persistence, widespread distribution, and potential risks to the environment and human health. This review focuses on the sources of MPs, their potential environmental risks, and human impacts, as documented in the recent literature from 2020 to 2026. Recent studies focusing on pathways, environmental weathering, and toxicity were evaluated and synthesized into the analysis. Previous studies have demonstrated that microplastics are transported across and between environmental compartments. Environmental degradation, driven by ultraviolet radiation, mechanical fragmentation, and oxidation, can alter microplastics’ surface characteristics, which may affect microplastic mobility, reactivity, and the solid-state adsorption of contaminants. Human exposure occurs primarily through ingestion and inhalation, with dermal and occupational exposure also contributing under certain conditions. Emerging evidence from in vitro, animal, and human tissue studies suggests that smaller particles, particularly nanoplastics, may contribute to oxidative stress, inflammation, and cellular injury; however, important uncertainties remain regarding environmentally realistic exposure levels, long-term health outcomes, and the extrapolation of experimental findings to real-world human health risk. Overall, the current literature highlights the need for standardized methodologies, improved integration of environmental monitoring and exposure assessment, and stronger evidence to support risk assessment and policy development. Full article

Per- and polyfluoroalkyl substances (PFASs) are persistent emerging contaminants characterized by high environmental stability and biotoxicity. Ubiquitous detection of these contaminants across aquatic environments poses severe threats to ecosystem stability and human health, while constructed wetlands (CWs) serve as a sustainable low-carbon alternative for the remediation of PFAS-laden wastewater. However, traditional mechanisms such as matrix adsorption, phytoaccumulation, and microbial transformation often suffer from low efficiency, rapid saturation, and incomplete degradation. To overcome the above drawbacks, the arbuscular mycorrhizal fungi (AMF)–plant–microbe synergistic consortium has become a promising remediation candidate, which facilitates PFAS immobilization and biodegradation via symbiotic crosstalk among three components. This paper reviews recent advancements in PFAS remediation within AMF-facilitated systems, examining fundamental synergistic mechanisms, treatment efficiencies, and key influencing factors. We propose several optimization strategies, including substrate modification, operational parameter refinement, and the integration of advanced technologies. Furthermore, we emphasize the necessity of elucidating the molecular pathways governing long-chain PFAS degradation and addressing current bottlenecks in engineering applications. Future research should prioritize molecular interaction level interaction mechanisms, the development of anti-interference systems, and field-scale validation. This review provides a theoretical foundation and technical framework for leveraging AMF–plant–microbe synergism to enhance PFAS removal in CWs. Full article

Frozen sand molds are the key material in digital frozen sand mold green casting technology, and their mechanical properties directly affect casting quality. Currently, these molds are primarily prepared by mechanical stirring, mixing, and compaction, which tend to cause imbalanced moisture adsorption and localized wet–dry differences, ultimately impairing the performance and quality of the castings. In this study, an ultrasonic vibration-assisted platform was established to prepare chromite sand frozen sand molds. By introducing ultrasonic vibration into the preparation process, a superior “sand grain–ice crystal” microstructure was constructed, leading to significantly enhanced mechanical properties. The tensile and compressive strengths were increased by approximately 10%, and the optimal process window for achieving the best mechanical performance of chromite sand was obtained. Full article

Tianjin, nestled on the North China Plain, possesses abundant geothermal resources with tremendous potential for development and utilization. This study employs hydrogeochemical and isotopic analysis techniques to thoroughly explore the geochemical characteristics and circulation patterns of geothermal fluids in Tianjin, shedding light on the mechanisms underlying the formation and evolution of deep geothermal fluids. The findings reveal that atmospheric precipitation serves as the primary recharge source for the region’s geothermal fluids, with the calculated recharge heights coinciding with those of the Jixian mountainous area. This precipitation infiltrates through permeable layers and the deep, large faults surrounding the southern plain, entering relatively enclosed or semi-enclosed geothermal reservoirs. As they circulate, the geothermal fluids undergo intricate interactions with the surrounding rocks, including processes such as leaching, adsorption, carbonate reprecipitation, cation exchange, and decarbonation. The fluids circulate at depths ranging from 1.6 to 3.5 km, with temperatures spanning from 67 to 133 °C. Along the flow path, the anionic composition of the geothermal fluids shifts from HCO₃⁻ dominance in the north to a coexistence of Cl⁻ and SO₄²⁻, ultimately dominated by Cl⁻ in the south, accompanied by an increase in total dissolved solids (TDS). The results indicate that Tianjin geothermal fluids are mainly recharged by meteoric water and evolve along their flow paths through dissolution of evaporitic and carbonate minerals, cation exchange, and carbonate precipitation. Hydrochemical and Sr-isotope differences suggest generally limited vertical connectivity among the studied reservoirs, although local hydraulic interaction may occur near conductive faults. These results provide constraints on the hydrogeochemical evolution and management of geothermal resources in the Tianjin sedimentary basin. Full article

The excessive emission of greenhouse gases (CO₂, CH₄, SF₆, and CF₄.) is a primary driver of global climate change, making the development of efficient adsorption and separation technologies critically important for achieving carbon reduction goals. Metal–organic frameworks (MOFs) have attracted considerable attention in this field due to their crystalline porous structures, ultrahigh surface areas, and tunable pore architectures. However, pristine MOFs face significant bottlenecks including poor water stability, high bed pressure drops caused by their powdered form, and limited mass transfer, which severely hinder their industrial application. The integration of MOFs with functional materials such as carbon materials, polymers, metal oxides, and porous SiO₂ offers a synergistic strategy to overcome these limitations. Carbon materials provide hydrophobic barriers and mesoporous transport channels, polymers enhance processability and mechanical strength, metal oxides introduce basic sites for enhanced chemisorption, and MOF-on-MOF heterostructures enable atomic-level interfacial integration and pore synergy. This review systematically summarizes recent advances in MOF composites for the separation of CO₂, CH₄, and fluorinated greenhouse gases (SF₆, CF₄.), with an emphasis on design strategies, structure–performance relationships, and synergistic mechanisms across different composite types. Finally, the current challenges including scalable synthesis, long-term stability, and separation performance under realistic conditions are discussed, and future directions toward rational design and functional synergy for industrial carbon capture and fluorinated gas emission reduction are envisioned. Full article

Amid growing pressure to reduce carbon emissions, carbon capture, utilization, and storage (CCUS) has become an important pathway toward deep decarbonization. However, the conventional separated “capture–release–conversion” process suffers from high energy consumption and system complexity, which severely limits its large-scale application. Integrated CO₂ Capture and Utilization (ICCU), which enables the capture, activation, and conversion of CO₂ within a single system, has attracted widespread attention because it can effectively reduce intermediate energy-intensive steps and improve carbon utilization efficiency. This review systematically summarizes recent progress in ICCU technology, with particular emphasis on reaction mechanisms and interfacial coupling characteristics. The performance features of solvent-based chemical absorption and solid-sorbent adsorption, two widely studied capture routes, are summarized, and typical integrated conversion pathways, including reverse water–gas shift, methanation, and dry reforming of methane, are discussed. On this basis, the roles of non-conventional energy-assisted strategies, such as photocatalysis, electrocatalysis, non-thermal plasma, and microwave irradiation, in expanding ICCU systems are further examined, together with their system-level coupling potential in carbon-intensive industries such as steel, cement, and power generation. Finally, the key scientific issues and engineering challenges currently facing ICCU are analyzed from the perspectives of fundamental mechanisms, material design, and system engineering, and future development directions are proposed. This review highlights that elucidating multiscale synergistic mechanisms, developing high-performance dual-function materials, and optimizing system integration are crucial to promoting the industrial application of ICCU technology. Full article