Search Results (309)

From an energetic, economic and environmental perspective, the selective removal of carbon dioxide and hydrogen sulfide from industrial natural gas streams is crucial. For this purpose, adsorption separation using nanoporous zeolites composed solely of silicon and oxygen atoms is a promising and environmentally friendly alternative to conventional adsorption and absorption processes. In this study, the adsorption of binary and ternary gas mixtures containing carbon dioxide, methane and/or hydrogen sulfide was examined with more than 100 different pure silica zeolites using atomic-resolution grand canonical Monte Carlo simulations. The IZA database was searched primarily for zeolites that could potentially be used to separate carbon dioxide from methane. However, many of the frameworks found were also suitable for the selective separation of hydrogen sulfide. The dependence of the calculated selectivities on pressure, temperature and gas composition was investigated, and a multi-step adsorption test was also performed with the zeolites showing the best performance. An empirical relationship was observed between certain structural parameters and the preference for binding carbon dioxide. This equation was then used to systematically screen a large database of theoretical zeolites. As a result, not only some IZA zeolites but also several theoretical zeolite structures were identified that strongly favor the adsorption of carbon dioxide over methane. Full article

Pt-rare earth metal (Pt-RE) alloys are considered to be one of the most promising electrocatalysts for producing oxygen reduction reactions (ORRs) due to their compressively strained Pt overlayer and their exceptional negative-alloy formation energies, which result in excellent activity and stability. However, there are still great challenges in the chemical synthesis of Pt-RE nanoalloys. Herein, we report a simple method employing the nanopores of porous carbon as nanoreactors to synthesize a Pt₅La nanoalloy. The Pt₅La alloy nanoparticles are embedded in porous carbon (Pt₅La@C) with a particle size of around 1–3 nm and also exhibit a very narrow size distribution because of the confined-space effect. The as-prepared Pt₅La@C nanoalloy exhibits highly efficient ORR performance with a half-wave potential of 0.912 V in 0.1 M HClO₄, which is 56 mV higher than that of a commercial Pt/C catalyst. Moreover, it achieves an improved intrinsic activity of 0.69 mA cm⁻² and, a mass activity of 0.42 A mg_Pt⁻¹ at 0.90 V. In addition, it also delivers a very stable lifespan performance, with negligible decay in half-wave potential after accelerated stress testing for 10,000 cycles. This work also provides a new method for the development of promising Pt-RE nanoalloys with ultrasmall nanoparticles with a very narrow size distribution for various efficient energy-conversion devices. Full article

Gas injection is a well-established method for enhancing oil recovery by improving oil mobility, primarily through viscosity reduction. While its application in heavy oil reservoirs is extensively studied, the specific impact of carbon dioxide (CO₂) injection pressure on fluid viscosity reduction and the ultimate recovery factor from light oil reservoirs has not been fully investigated. To address this gap, this experimental study systematically explores the effects of CO₂ injection pressure and reservoir permeability on light oil recovery. This study conducted miscible, near-miscible, and immiscible gas injection experiments on two core samples with distinct permeabilities (13.4 md and 28 md), each saturated with light oil. CO₂ was injected at five different pressures, including conditions ranging from immiscible to initial reservoir pressure. The primary metrics for evaluation were the recovery factor (measured at gas breakthrough, end of injection, and abandonment pressure) and the viscosity reduction of the produced oil. The results conclusively demonstrate that CO₂ injection significantly enhances light oil production. A direct proportional relationship was established between both the injection pressure and the recovery factor and between permeability and overall oil production at the gas breakthrough. However, a key finding was the inverse relationship observed between permeability and viscosity reduction: the lower-permeability sample (13.4 md) consistently exhibited a greater percentage of viscosity reduction across all injection pressures than the higher-permeability sample (28 md). This unexpected trend is aligned with the inverse relationship between the permeability and the recovery factor after the gas breakthrough. This outcome suggests that enhanced CO₂ solubility, driven by higher confinement pressures within the nanopores of the lower-permeability rock, promotes a localized, near-miscible state. This effect was even evident during immiscible injection, where the low-permeability sample showed a noticeable viscosity reduction and superior long-term production. These findings highlight the critical role of pore-scale confinement in governing CO₂ miscibility and its associated viscosity reduction, which should be incorporated into enhanced oil recovery design for unconventional reservoirs. Full article

Nanoporous gold (np-Au) has attracted significant attention for biomedical and electrochemical applications due to its high surface area, tunable morphology, and excellent biocompatibility. In this study, polycrystalline gold surfaces were modified by anodization in 0.3–0.9 M oxalic acid to produce np-Au layers. The influence of anodization conditions on surface morphology, chemical composition, electronic properties, and corrosion resistance in artificial saliva was systematically investigated. Surface morphology and porosity were analyzed by scanning electron microscopy combined with image analysis, revealing a transition from fine and uniform porosity to highly developed but structurally heterogeneous nanoporous structures with increasing oxalic acid concentration. Energy-dispersive spectroscopy confirmed surface oxidation and adsorption of oxygen- and carbon-containing species after anodization, while gold remained the dominant component. Scanning Kelvin probe measurements demonstrated significant modifications of surface electronic properties, including changes in contact potential difference, governed by nanostructure geometry and surface chemistry. Electrochemical tests in artificial saliva showed that increasing nanoporousness led to reduced thermodynamic stability, with the sample anodized in 0.3 M oxalic acid providing the most favorable balance between corrosion resistance and surface activity. These results demonstrate that oxalic acid anodization is a simple and effective approach for tailoring gold surfaces for biomedical applications, particularly in dentistry. Full article

P-cresol, indole and indole-3-acetic acid (IAA) are catabolites of amino acids, formed by the gut microbiome. Most of these aromatic hydrocarbon derivatives are excreted by the colon before reentering the body to form “exogenous” protein-bound uremic toxins (PBUTs), which aggravate chronic kidney disease (CKD). Removal efficiencies of these PBUT precursors from model phosphate-buffered saline solutions by three different surface-modified nanoporous carbon adsorbents (PCs) were studied. PCs were produced by physicochemical and/or acid base activation of carbonized rice husk waste. Removal rates achieved values of 32–96% within a 3 h contact time. High micro/mesoporosity and surface chemistry of the N- and P-doped biochars were established by N₂ adsorption studies, SEM/EDS analysis, XPS and FT-IR-spectroscopy. The ammoxidized PC-N1 had the highest adsorption capacity (1.97 mmol/g for IAA, 2.43 mmol/g for p-cresol and 2.42 mmol/g for indole), followed by “urea-nitrified” PC-N2, whilst the phosphorylated PC-P demonstrated the lowest adsorption capacity for these solutes. These results do not correlate with the total pore volume values for PC-N2 (0.91 cm³/g) < PC-P (1.56 cm³/g) < PC-N1 (1.84 cm³/g), suggesting that other parameters such as the micropore volume (PC-N1 > PC-N2 > PC-P) and the interaction of surface chemical functional groups with the solutes play key roles in the adsorption mechanism. N-doped PC-N1 and PC-N2 have basic functional groups with higher affinity with acidic IAA and p-cresol. The ion-exchange mechanism of phenolic and indolic compound chemisorption by nanoporous carbon adsorbents, modified with surface N- and P-containing functional groups, has been proposed. Full article

The characteristics of shale oil reservoirs, such as low porosity, ultra-low permeability, and complex pore structure, are key factors affecting effective pore space and fluid migration. This study focuses on medium-to-high maturity mud shale in the Qing-1 Member of the Qingshankou Formation in the Gulong Sag. Using methods such as XRD, organic geochemical testing, and multi-scale pore characterization (FE-SEM, low-temperature CO₂–N₂ adsorption, high-pressure mercury intrusion, and CT scanning), the lithofacies and pore structure were comprehensively characterized, and their controlling factors were analyzed. The results indicate: (1) The mineral composition is dominated by felsic and clay minerals. Based on a three-level classification standard of “mineral composition–sedimentary structure–organic matter abundance”, seven subfacies were identified, with the dominant lithofacies being Felsic–Clayey Mixed Shale and Felsic-bearing Clay Shale. (2) The reservoir space consists of inorganic pores, organic pores, microfractures, and a small amount of other auxiliary pores, exhibiting “bimodal” pore size characteristics. Micro–mesopores dominate adsorption, while macropores/microfractures control free oil seepage; mesopores contribute the most to pore volume. (3) In terms of oil-bearing potential, Felsic–Clayey Mixed Shale shows prominent movable oil potential (average OSI: 133.08 mg/g; S₁ > 2 mg/g, OSI > 100 mg/g). (4) CT-based 3D stick-and-ball models indicate that Felsic–Clayey Mixed Shale has the best connectivity (connectivity rate: 30.63%), with throat radii mostly ranging from 1–15 μm and pore radii from 2–20 μm. (5) Pore development is synergistically controlled by total organic carbon (TOC, with an optimal range of approximately 1–2.5%), clay/felsic mineral ratio, and bedding/structural fractures. The formation of the pore system is the result of dynamic coupling of organic–inorganic interactions during diagenetic evolution: intergranular pores of clay minerals and microfractures jointly contribute to specific surface area and pore volume, while bedding fractures connect nanopore clusters to enhance seepage capacity. This study improves the integrated understanding of dominant lithofacies, pore structure, and oil-bearing potential in the Qing-1 Member of the Gulong Sag, providing a basis for sweet spot evaluation and development optimization. Full article

This study reports the synthesis of an activated nanoporous carbon material from Phyllanthus emblica (Amala)—a biomass material which is an eco-friendly, economical, and sustainable precursor used to prepare activated carbon using zinc chloride (ZnCl₂) activation at various temperatures (500–700 °C) under a nitrogen gas atmosphere. A sample that was carbonized at 700 °C (AmC_Z700) attained a high specific surface area of 1436 m² g⁻¹ and a total pore volume of 0.962 cm³ g⁻¹, and, when used in an electrode, showed excellent supercapacitance performance, attaining a high specific capacitance of 263 F g⁻¹ at a current density of 1 A g⁻¹, followed by 55% capacitance retention at 50 A g⁻¹. Additionally, the assembled symmetric supercapacitor cell, when operated at 1.2 V, delivered an energy density of 8.9 Wh kg⁻¹ at a power density of 300 W kg⁻¹ and exhibited an excellent cycle life of 95% after 10,000 successive charge/discharge cycles, demonstrating the substantial potential of Phyllanthus emblica seed-derived carbon materials for the creation of high-performance supercapacitors. Full article

To clarify the organic matter enrichment regularity of Permian shales in the Kaijiang–Liangping Trough, as well as the differential characteristics of their reservoir lithology, mineral assemblage, and nanopore structure—and thereby provide a geological basis for the exploration and development of Permian marine shales in the eastern Sichuan Basin—core samples from different depths of the Wujiaping Formation and Dalong Formation in Well DY-1H were analyzed using a series of micro–nano technical research methods, including whole-rock X-ray diffraction, major/trace element analysis, conventional porosity-permeability measurement, high-pressure mercury intrusion porosimetry, nitrogen adsorption, and field emission scanning electron microscopy. Research finds that the Dalong Formation shale contains Type I organic matter with high abundance, whereas the Wujiaping Formation shale is dominated by Type II₂ organic matter. The Wujiaping Formation experienced stronger terrigenous input and higher weathering intensity, while the Dalong Formation was deposited under persistently anoxic conditions, in contrast to the frequent oxic–anoxic alternations in the Wujiaping Formation. Paleoproductivity indicators suggest higher productivity in the Dalong Formation than in the Wujiaping Formation. Mo/TOC ratios below 4.5 indicate deposition in a strongly restricted water body. Enrichment factors of multiple elements further support the enhanced paleoproductivity of the Dalong Formation. The Dalong Formation shale has higher contents of quartz and carbonate minerals, while the Wujiaping Formation shale has a higher content of clay minerals. The Wujiaping Formation shale is more developed with inorganic micropores, whereas the Dalong Formation shale is characterized by more developed organic nanopores. During the sedimentary period of the Dalong Formation shale, the paleoproductivity was high, the sedimentary waterbody had high reducibility and restriction, and the reservoir was well-developed with nanopores. The Dalong Formation is a more favorable interval for Permian shale gas exploration and development in the Kaijiang–Liangping Trough. Full article

Electrocatalytic water splitting for hydrogen production is a crucial technology in achieving carbon neutrality. The development of efficient and stable hydrogen evolution reaction (HER) electrocatalysts is a core challenge in this field. This review systematically summarizes the latest research advancements in nanoporous transition metal-based catalysts, covering metal alloys and compounds. Through strategies such as compositional optimization, crystal structure modulation, interface engineering, and nanoporous structure design, these non-precious metal catalysts exhibit outstanding performance comparable to commercial platinum-carbon catalysts across a wide pH range. This paper thoroughly discusses the catalytic mechanisms of different material systems, including electronic structure regulation, active site exposure, and mass transport optimization. Finally, the challenges faced in current research are summarized, and future directions are projected, including scalable fabrication processes and performance validation in real electrolysis cell environments. This review provides significant insights into designing next-generation efficient and stable non-precious metal electrocatalysts. Full article

Methodological fusion of materials chemistry, which enables us to create materials, with nanotechnology, which enables us to control nanostructures, could enable us to create advanced functional materials with well controlled nanostructures. Positioned as a post-nanotechnology concept, nanoarchitectonics will enable this purpose. This review paper highlights the broad scope of applications of the new concept of nanoarchitectonics, selecting and discussing recent papers that contain the term ‘nanoarchitectonics’ in their titles. Topics include controls of dopant atoms in solid electrolytes, transforming the framework of carbon materials, single-atom catalysts, nanorobots and microrobots, functional nanoparticles, nanotubular materials, 2D-organic nanosheets and MXene nanosheets, nanosheet assemblies, nitrogen-doped carbon, nanoporous and mesoporous materials, nanozymes, polymeric materials, covalent organic frameworks, vesicle structures from synthetic polymers, chirality- and topology-controlled structures, chiral helices, Langmuir monolayers, LB films, LbL assembly, nanocellulose, DNA, peptides bacterial cell components, biomimetic nanoparticles, lipid membranes of protocells, organization of living cells, and the encapsulation of living cells with exogenous substances. Not limited to these examples selected in this review article, the concept of nanoarchitectonics is applicable to diverse materials systems. Nanoarchitectonics represents a conceptual framework for creating materials at all levels and can be likened to a method for everything in materials science. Developing technology that can universally create materials with unexpected functions could represent the final frontier of materials science. Nanoarchitectonics will play a significant part in achieving this final frontier in materials science. Full article

Efficient coalbed methane (CBM) recovery combined with carbon dioxide (CO₂) sequestration is a promising strategy for sustainable energy production and greenhouse gas mitigation. However, the molecular mechanisms controlling pressure-dependent CH₄ displacement by CO₂ in coal nanopores remain insufficiently understood. In this study, molecular dynamics simulations were conducted to investigate CO₂-driven CH₄ recovery in a slit-pore coal model under driving pressures of 15, 20, and 25 Mpa. The simulations quantitatively captured the competitive adsorption, diffusion, and migration behaviors of CH₄, CO₂, and water, providing insights into how pressure influences enhanced coalbed methane (ECBM) recovery at the nanoscale. The results show that as the pressure increases from 15 to 25 Mpa, the mean residence time of CH₄ on the coal surface decreases from 0.0104 ns to 0.0087 ns (a 16% reduction), reflecting accelerated molecular mobility. The CH₄–CO₂ radial distribution function peak height rises from 2.20 to 3.67, indicating strengthened competitive adsorption and interaction between the two gases. Correspondingly, the number of CO₂ molecules entering the CH₄ region grows from 214 to 268, demonstrating higher invasion efficiency at elevated pressures. These quantitative findings illustrate a clear shift from capillary-controlled desorption at low pressure to pressure-driven convection at higher pressures. The results provide molecular-level evidence for optimizing CO₂ injection pressure to improve CBM recovery efficiency and CO₂ storage capacity. Full article

The significant heterogeneity of continental shale reservoirs within the Permian Lucaogou Formation of the Jimsar Sag presents a major challenge for shale oil exploration. This study aims to quantitatively characterize the pore structure complexity of different lithofacies to identify favorable “sweet spots.” By integrating geochemical, petrological, and high-resolution pore characterization data with fractal theory, we introduce a comprehensive fractal dimension (D_c) for evaluation. Five distinct lithofacies are identified: massive felsic siltstone (MFS), bedded dolostone (BD), bedded felsic dolostone (BFD), laminated dolomitic felsic shale (LDFS), and laminated mud felsic shale (LMFS). Pore structures vary significantly: MFS is dominated by mesopores (100–2000 nm), BD and BFD exhibit a bimodal distribution (<30 nm and >10 μm), while LDFS and LMFS are characterized by nanopores (<50 nm). D_c analysis reveals a descending order of pore structure complexity: BFD > LMFS > LDFS > MFS > BD. Furthermore, D_c shows positive correlations with clay mineral and feldspar contents but a negative correlation with carbonate minerals. A significant negative correlation between D_c and measured permeability confirms its effectiveness in characterizing reservoir heterogeneity. We propose that MFS and LDFS, with higher pore volumes and relatively lower D_c values, represent the most favorable targets due to their superior storage and seepage capacities. This study provides a theoretical foundation for the efficient development of continental shale oil reservoirs. Full article

The conversion of low-grade heat into storable electrical energy using nanoporous carbon materials represents an efficient energy harvesting strategy. In this study, a reduced graphene oxide (RGO) and carbon nanotube (CNT) composite with a rich microporous structure was synthesized. A symmetrical thermoelectric cell was constructed to harvest thermal energy. The application of a temperature difference (ΔT) generated a stable equilibrium voltage (U_s), which scaled linearly with ΔT. The resulting thermoelectric coefficient (U_s/ΔT) increased markedly with the carbon nanotube (CNT) content, underscoring the effectiveness of CNT incorporation for improving thermoelectric properties. It also shows a non-monotonic dependence on KCl concentration, first increasing and then decreasing, with a maximum value of 4.17 mV/°C achieved in 0.1 M KCl using the RGO-5%CNTs electrode. When connected to an external load, the discharge voltage and current decay rapidly before stabilizing within seconds. Circuit analysis reveals that the incorporation of CNTs reduces internal resistance and increases the equivalent capacitance. Although instantaneous discharge power declines quickly, the addition of CNTs elevates its initial value and slows the decay rate. Both the average output power and thermoelectric conversion efficiency improve with increasing ΔT and are further enhanced at higher CNT content. Overall, the RGO-CNT composite demonstrates significantly superior thermoelectric performance compared to pure RGO. Full article

In response to the growing complexity of global exploration targets, traditional Euclidean geometric and linear statistical methods reveal inherent theoretical limitations in characterizing hydrocarbon reservoirs as complex geological bodies that exhibit simultaneous local disorder and global order. Fractal theory, with its core parameter systems such as fractal dimension and scaling exponents, provides an innovative mathematical–physics toolkit for quantifying spatial heterogeneity and resolving the multi-scale characteristics of reservoirs. This review systematically consolidates recent advancements in the application of fractal theory to oil and gas resource assessment, with the aim of elucidating its transition from a theoretical concept to a practical tool. We conclusively demonstrate that fractal theory has driven fundamental methodological progress across four critical dimensions: (1) In reservoir classification and evaluation, fractal dimension has emerged as a robust quantitative metric for heterogeneity and facies discrimination. (2) In pore structure characterization, the theory has successfully uncovered structural self-similarity across scales, from nanopores to macroscopic vugs, enabling precise modeling of complex pore networks. (3) In seepage behavior analysis, fractal-based models have significantly enhanced the predictive capacity for non-Darcy flow and preferential migration pathways. (4) In fracture network modeling, fractal geometry is proven pivotal for accurately characterizing the spatial distribution and connectivity of natural fractures. Despite significant progress, current research faces challenges, including insufficient correlation with dynamic geological processes and a scarcity of data for model validation. Future research should focus on the following directions: developing fractal parameter inversion methods integrated with artificial intelligence, constructing dynamic fractal–seepage coupling models based on digital twins, establishing a unified fractal theoretical framework from pore to basin scale, and expanding its application in low-carbon energy fields such as carbon dioxide sequestration and natural gas hydrate development. Through interdisciplinary integration and methodological innovation, fractal theory is expected to advance hydrocarbon resource assessment toward intelligent, precise, and systematic development, providing scientific support for the efficient exploitation of complex reservoirs and the transition to green, low-carbon energy. Full article

This review establishes a comprehensive technical framework for aerogel-based fire-resistant coatings, from fundamental mechanisms to industrial applications. It analyses the multi-mode flame-retardant and thermal insulation mechanisms achieved through aerogels’ synergistic suppression of heat conduction, convection, and radiation, establishing their theoretical basis. The work compares the intrinsic characteristics of silica-based, carbon-based, and bio-based aerogels, providing rational selection criteria for fire protection systems. The study examines key integration challenges: balancing nanopore preservation with interfacial compatibility, inherent mechanical weaknesses, conflicts between high filler loading and workability, and scalability issues. It evaluates targeted strategies including interface engineering, mechanical reinforcement, workability optimization, and low-cost production routes. Application prospects in construction, tunneling, and cable protection are outlined. This review provides a coherent progression from mechanisms and material properties to challenges and solutions, offering theoretical guidance and a technical roadmap for developing next-generation high-performance fire-resistant coatings. Full article