Search Results (120)

Porous carbon from renewable resources like biomass is a key material utilized in many applications ranging from environmental remediation to energy storage. There are limited reports in the literature on the effects of biomass pretreatment, production process parameters, and downstream processing on the final product properties. This is the first study aimed at closing the latter research gap. Six different types of underutilized biomass were examined: eastern red cedar wood, pecan shells, hazelnut shells, algal biomass, miscanthus, and sludge produced at municipal wastewater treatment facilities. Although pretreatment of biomass with KOH or ZnCl₂ enhanced formation of micro- and mesopores, carbon yield was lower (15.3–32.5%) than that obtained via non-catalytic pyrolysis (28.3–48%). An optimization study performed using response surface methodology and cedar wood has shown the significant effects (p < 0.05) of temperature and catalyst/biomass ratio on total BET pore volume and surface area. Additionally, catalyst/biomass ratio had a significant effect on the crystal structure and pore size distribution in the carbon produced by pyrolysis. Hence, optimization of process temperature, hold time, and activation ratio is capable of yielding porous carbon from cedar wood pyrolysis with desirable properties. Full article

Carbonation–calcination looping using CaO-based natural sorbents such as limestone is a promising technology for the capture of CO₂ from fossil fuel-based power plants. In this study, the CO₂ capture capacities of Buipe, Oterpkolu, and Nauli limestones from quarries in Ghana were measured in a laboratory-scale micro-fluidized bed reactor through multiple carbonation–calcination cycles. The changes in CO₂ capture capacity and conversion with the number of cycles mostly correlated with the changes in the physico-chemical properties: Capture capacity dropped from >60% to <15% after 15 cycles and the surface area dropped to below 5 m² g⁻¹ from as much as 20 m² g⁻¹ (for the Oterkpolu). The pore volume of the Nauli limestone was essentially invariant with the number of cycles while it increased for the Buipe limestone, and initially increased and then dropped for the Oterpkolu limestone. This decrease was likely due to sintering and a reduction in the number of micropores. The unusual increase in pore volume after multiple cycles was due to the formation of mesopores with smaller pore diameters. Full article

The development of cost-effective and scalable air/oxygen electrode materials is crucial for the advancement of Zn–air batteries (ZABs). Porous carbon materials doped with heteroatoms have attracted considerable attention in energy and environmental fields because of their tunable nanoporosity and high electrical conductivity. In this work, we report the synthesis of a three-dimensional (3D) N and P co-doped porous carbon (PA@pDC-1000), derived from a conjugated polyaniline–phytic acid polymer. The cross-linked, rigid conjugated polymeric framework plays a crucial role in maintaining the integrity of micro- and mesoporous structures and promoting graphitization during carbonization. As a result, the material exhibits a hierarchical pore structure, a high specific surface area (1045 m² g⁻¹), and a large pore volume (1.02 cm³ g⁻¹). The 3D N, P co-doped PA@pDC-1000 catalyst delivers a half-wave potential of 0.80 V (vs. RHE) and demonstrates a higher current density compared to commercial Pt/C. A primary ZAB utilizing this material achieves an open-circuit voltage of 1.51 V and a peak power density of 217 mW cm⁻². This metal-free, self-templating presents a scalable route for the generating and producing of high-performance oxygen reduction reaction catalysts for ZABs. Full article

Controlled porosity with precise pore sizes in carbon monoliths (CMs) is crucial for optimizing performance in electrochemical energy storage and adsorption applications. This study explores the influence of porosity in CMs, developed from polymer precursors via the sol–gel route, employing soft templating, in situ graphene growth, and post-activation. The effects on CO₂ and H₂ sorption and electrochemical capacitor (EC) performance are analyzed. Graphene is successfully grown in situ from graphene oxide (GO), as confirmed by several characterization analyses. The amount of GO incorporated influences the crosslink density of the polymer gel, generating various pore structures at both micro- and mesoscales, which impacts performance. For instance, CO₂ capture peaks at 5.01 mmol g⁻¹ (0 °C, 101 kPa) with 10 wt % GO, due to the presence of wider micropores that allow access to ultramicropores. For H₂ storage, the best performance is achieved with 5 wt % GO, reaching 12.8 mmol g⁻¹ (−196 °C, 101 kPa); this is attributed to the enlarged micropore volumes between 0.75 and 2 nm that are accessible by mesopores of 2 to 3 nm. In contrast, for the ECs, lower GO loadings (0.5 to 2 wt %) improve ion accessibility via mesopores (4 to 6 nm), enhancing rate capability through better conduction. Full article

Heterogeneity of pore and fracture structures has become an important factor affecting the migration of methane and water in coal reservoirs. However, controlling factors of pore and fracture structure collected from coal seam 10 in Taliqike Formation, Kubai Coalfield, Xinjiang need to be studied. In this paper, carbon dioxide adsorption, cryogenic liquid nitrogen, and high-pressure mercury intrusion, as well as coal microscopic components, were used to study pore volumes and characterize pore diameter distribution heterogeneity. By the theory of single weight and multiple fractal formations, the heterogeneity of the pore fracture structure of coal reservoir is expressed, and the influencing factors of the heterogeneity of the pore fracture structure and the pore volume are also discussed. The results are as follows. (1) Micro-pore distribution presents a distinct bidirectional state, with the main peak at approximately 0.6 nm and 0.85 nm. R_o,max has an obvious influence on micro-pore volume. The single-fractal dimension of micro-pore is not affected by a micro-pore volume but is influenced by other factors such as R_o,max and microscopic composition. The heterogeneity of the low-value area controls the heterogeneity of micro-pore diameter distribution. (2) For lower R_o,max samples, mesopores of these samples are ink bottle-shaped pores, and the pore connectivity is poor. In contrast, meso-pore of higher thermal evolution coal samples are mostly simple pores, such as parallel plates. The main mesopores are 10–100 nm pores, accounting for 75% of the total meso-pore volume. For the single fractal dimension, D₁ is greater than D₂, which also shows that the heterogeneity of a pore structure greater than 4 nm is much stronger than that of a pore structure less than 4 nm in these samples. (3) For lower R_o,max samples, double S-shaped curves with distinct hysteresis loop are obtained, while samples of higher R_o,max samples show parallel curves, suggesting that macro-pore of this type of sample develops parallel plate-like pore. There is a positive relationship between D₋₁₀–D₀ and D₋₁₀–D₁₀, while D₀–D₁₀ and D₋₁₀–D₀ have a weak correlation. With the increase of 2–10 nm pore volume, pore distribution heterogeneity of lower value area (D₋₁₀–D₀) weakens. This indicates that pore volume is an important factor affecting the multifractal variation. Full article

Pore structure plays a critical role in evaluating shale “sweet spots”. Compared to marine shale, lacustrine shale has more diverse lithofacies types and greater heterogeneity in pore structure due to frequently changing environmental conditions. Using methods such as mercury intrusion porosimetry (MIP), field emission scanning electron microscopy (FE-SEM), nuclear magnetic resonance (NMR), and X-ray diffraction (XRD), this study investigates the micropore structures and heterogeneity of different lithofacies in the Jurassic Dongyuemiao Member lacustrine shale. Image processing and multifractal theory were employed to identify the controlling factors of pore structure heterogeneity. The key findings are as follows. (1) Based on mineral content and laminae types, the lithofacies types of Dongyuemiao lacustrine shale are classified into four types: shell–laminae mixed shale (SLMS), silty–laminae clay shale (SLCS), clast–laminae clay shale (CLCS), and clay shale (CS). (2) Based on genesis, shale reservoirs’ pore and permeability space are categorized into inorganic pores, organic pores, and micro-fractures. Inorganic pores consist of inter-particle pores and intra-particle pores. Pore size distribution curves for all four lithofacies exhibit two main peaks, with pore sizes concentrated in the ranges of 2–10 nm and 50–80 nm. Mesopores and macropores dominate, accounting for over 80% of the total pore volume. Mesopores are most developed in CLCS, representing 56.3%. (3) Quartz content is positively correlated with the multifractal dimension, while clay content shows a negative correlation. Higher quartz content, coupled with lower clay content, weakens pore structure heterogeneity. A negative correlation exists between total organic carbon (TOC) and the multifractal dimension, indicating that higher organic matter content enhances organic pore development and increases microscopic heterogeneity. (4) Porosity heterogeneity in SLMS is effectively characterized by D₀-D_max, while in the other three lithofacies, it is characterized by D_min-D₀. Permeability across all lithofacies correlates with D₀-D_max. In CS, SLMS, and SLCS, permeability is positively correlated with D₀-D_max, with higher values indicating greater permeability heterogeneity. In CLCS, permeability is negatively correlated with D₀-D_max, such that lower values reflect stronger heterogeneity. Full article

The development of carbonaceous materials such as biochar has triggered a hot spot in materials application. In this study, a new type of char carbon was developed from raw cigarette filter rods (CFRs) via a carbonization process under moderate conditions (T = 550 °C; t_res = 1 h) (CFR char carbon). The produced char was characterized by ATR-FTIR (Attenuated total reflectance—Fourier-transform infrared) spectroscopy, XRD (X-ray diffraction) analysis, GC-MS (Gas Chromatography–Mass Spectrometry), FESEM-EDS (Field-Emission Scanning Electron Microscopy—Energy-dispersive X-ray spectroscopy) technique, XPS (X-ray photoelectron spectroscopy), and N₂ adsorption/desorption (BET) measurements. The obtained carbon material is rich in oxygen-containing functional groups (i.e., C=O, C–O, –C(=O)–CH₃, C–O–C, C–OH, and O=C–O, with chemisorbed oxygen), containing significant amounts of calcium (that originates from CaCO₃) and silicon (Si), generated by reduction of SiO₂. It was found that the formation of char(C)/n-alkane composite material makes that CFR char have a high compressive strength improvement. Moderate carbonization has contributed to the creation of such material that has a fairly high specific surface area (320.93 m²/g), exhibiting a complex hierarchical structure that was characterized by composite Type I/IV(a) isotherm, associated with micro-/mesoporous carbon material. In addition, more directional extensions of this research for future work were proposed, including the implementation of electrochemical research. Full article

The aim of this paper was to obtain activated biocarbons from the natural biomass of horse chestnut seeds (Aesculus hippocastanum) by physical activation with two different activating agents, carbon dioxide and water vapor, and to evaluate their structural and adsorption properties. The effect of the pyrolysis atmosphere on the surface development and porosity as well as the structure and adsorption properties of the materials in relation to the selected organic adsorbates (tetracycline (TC), naproxen (NPX), and methyl orange (MO)), which may constitute a potential contamination of the aquatic environment, was evaluated. Activated biocarbons were characterized using N₂ low-temperature adsorption/desorption, Raman and FT-IR spectroscopy, and thermogravimetric analysis (TGA). The nature of the surface (pH_pzc and Boehm titration) was also studied. Micro/mesoporous biocarbons were obtained with an S_BET area in the range of ~534 to 646 m²/g, in which micropores constituted ~70%. It was proved that the obtained materials are characterized by high adsorption values (~120 mg/g, ~150 mg/g, and ~252 mg/g) and removal rates %R (~80%, ~95%, and ~75%) for TC, NPX, and MO, respectively. The results indicate that chestnut-derived activated biocarbons are a promising, cost-effective and environmentally friendly alternative for removing organic contaminants from aqueous solutions. Future research should focus on optimizing activation parameters and assessing the long-term performance of adsorbents. Full article

The wastewater of the “Rubizhanskyi” storage facility at the chemical enterprise “Rubizhanskyi Krasitel” (Ukraine) is a complex multicomponent system. The concentration of colored organic substances in the highly mineralized wastewater significantly exceeds the established norms. This work shows the possibility of an almost complete purification of the multicomponent wastewater using a carbon sorbent. The treatment of wastewater was carried out using the sorption method with carbon adsorbents KARBON™ (Institute for Sorption and Problems of Endoecology, Kyiv, Ukraine) and ZL-302, which are micro-mesoporous materials, with specific surface areas of 1730 and 1523 m²/g, respectively. The purification efficiency of the wastewater containing aromatic compounds by the carbon adsorbents KARBON™ and ZL-302 achieved 99.99% and 94.4%, respectively. The adsorption capacity of the carbon adsorbent KARBON™ with respect to aniline was 0.47 g/g, and that of commercial coal ZL-302 was 0.45 g/g. Therefore, the carbon adsorbent KARBON™ is a promising material for the successful purification of wastewater from chemical enterprises contaminated with aromatic compounds. Full article

The electrochemical properties of the hydrophobic room-temperature ionic liquid 1-propyl-2,3-dimethylimidazolium bis(trifluoromethylsulfonyl)imide (PMMIm(TFSI)) were investigated, for the first time, using an electrochemical double-layer capacitor-mimicking cell containing two identical-sized micro–mesoporous molybdenum carbide-derived carbon electrodes (MMP-C(Mo₂C)), by applying cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) techniques. Surprisingly, despite the substitution of the slightly acidic hydrogen atom with a methyl group at the carbon atom located between two nitrogen atoms in the imidazolium cation, the EIS and CV measurements demonstrated that PMMIm(TFSI) began to decompose electrochemically at the same cell potential (ΔE) as 1-ethyl-3-methylimidazolium tetrafluoroborate (EMIm(BF₄)), specifically at ΔE = 2.75 V. However, the CV and EIS data indicated that PMMIm(TFSI) decomposed with a significantly lower intensity than EMIm(BF₄). Therefore, we believe that the use of PMMIm(TFSI) as the electrolyte will enable the construction of safer supercapacitors that can tolerate short periods of over-polarization up to ΔE = 4.0 V. However, when the ΔE ≤ 3.2 V was applied, EMIm(BF₄) offered higher maximum power compared to PMMIm(TFSI). We found that the calculated maximum gravimetric power precisely describes the maximum ΔE applicable for a supercapacitor candidate. Full article

This review analyzes the current practices in the data-driven characterization, design and optimization of disordered nanoporous materials with pore sizes ranging from angstroms (active carbon and polymer membranes for gas separation) to tens of nm (aerogels). While the machine learning (ML)-based prediction and screening of crystalline, ordered porous materials are conducted frequently, materials with disordered porosity receive much less attention, although ML is expected to excel in the field, which is rich with ill-posed problems, non-linear correlations and a large volume of experimental results. For micro- and mesoporous solids (active carbons, mesoporous silica, aerogels, etc.), the obstacles are mostly related to the navigation of the available data with transferrable and easily interpreted features. The majority of published efforts are based on the experimental data obtained in the same work, and the datasets are often very small. Even with limited data, machine learning helps discover non-evident correlations and serves in material design and production optimization. The development of comprehensive databases for micro- and mesoporous materials with low-level structural and sorption characteristics, as well as automated synthesis/characterization protocols, is seen as the direction of efforts for the immediate future. This paper is written in a language readable by a chemist unfamiliar with the data science specifics. Full article

Carbon is predominantly used in zinc-ion hybrid capacitors (ZIHCs) as an electrode material. Nitrogen doping and strategic design can enhance its electrochemical properties. Melamine formaldehyde resin, serving as a hard carbon precursor, synthesizes nitrogen-doped porous carbon after annealing. Incorporating transition metal catalysts like Ni, Co, and Fe alters the morphology, pore structure, graphitization degree, and nitrogen doping types/proportions. Electrochemical tests reveal a superior capacitance of 159.5 F g⁻¹ at a scan rate of 1 mV s⁻¹ and rate performance in Fe-catalyzed N-doped porous carbon (Fe-NDPC). Advanced analysis shows Fe-NDPC’s high graphitic nitrogen content and graphitization degree, boosting its electric double-layer capacitance (EDLC) and pseudocapacitance. Its abundant micro- and mesopores increase the surface area fourfold compared to non-catalyzed samples, favoring EDLC and fast electrolyte transport. This study guides catalyst application in carbon materials for supercapacitors, illuminating how catalysts influence nitrogen-doped porous carbon structure and performance. Full article

With the evolution of unconventional oil and gas exploration concepts from source rocks and reservoirs to carrier beds, the inter-layer sandstone carrier bed within marine–continental transitional shale strata has emerged as a significant target for oil and gas exploration. The inter-layer sandstone is closely associated with the source rock and differs from conventional tight sandstone in terms of sedimentary environment, matrix composition, and the characteristics of reservoir microscopic pore development. Preliminary exploration achievements display that the inter-layer sandstone is plentiful in gas content and holds promising prospects for exploration and development. Consequently, it is essential to investigate the gas-rich accumulation theory specific to the inter-layer sandstone reservoir in transitional facies. Pore development characteristics and heterogeneity are crucial aspects of oil and gas accumulation research, as they influence reservoir seepage performance and capacity. This paper employs total organic carbon analysis, X-ray diffraction, rock thin section examination, field emission scanning electron microscopy, physical analysis, high-pressure mercury intrusion analysis, gas adsorption experiments, and fractal theory to explore the reservoir development characteristics of the sandstone samples from the Upper Permian marine–continental transitional facies Longtan Formation in the southern Sichuan Basin. It also attempts to combine high-pressure mercury intrusion analysis and gas adsorption experiments to describe the structural and fractal characteristics of pores at different scales in a segmented manner. The findings reveal that the sandstone type of the Longtan Formation is mainly lithic sandstone. The pore size distribution of the sandstone primarily falls below 30 nm and above 1000 nm, with the main pore types being inter-granular pores and micro-fractures in clay minerals. The pore volume and specific surface area are largely attributed to the micropores and mesopores of clay minerals. The pore morphology is complex, exhibiting strong heterogeneity, predominantly characterized by slit-like and ink bottle-like features. Notably, there are discernible differences in reservoir structural characteristics and homogeneity between muddy sandstone and non-muddy sandstone. The pore morphology is complex, exhibiting strong heterogeneity, predominantly characterized by slit-like and ink bottle-like features. Notably, there are discernible differences in reservoir structural characteristics and homogeneity between muddy sandstone and non-muddy sandstone. Full article

Currently, materials with specific, strictly defined functional properties are becoming increasingly important. A promising strategy for achieving these properties involves developing methods that facilitate the formation of hierarchical porous materials that combine micro-, meso-, and macropores in their structure. Macropores facilitate effective mass transfer of substances to the meso- and micropores, where further adsorption or reaction processes can occur. Aerogels represent a promising class of materials for implementing this approach. The formation of hierarchical porous structures in aerogels can be achieved using soft and hard templating methods or by foaming techniques. This paper presents a comprehensive study of three methods for forming hierarchical porous structures in alginate aerogels: (1) employing surfactants (Pluronic F-68), (2) using zein as a pore-forming component, and (3) foaming in a carbon dioxide medium. The results of micro-CT showed that each of the methods contributes to the formation of macropores within the structure of the resulting aerogels. Size distribution curves of the detected macropores were obtained, showing the presence of macropores ranging from 16 to 323 μm in size for samples obtained using surfactants, from 5 to 195 μm for samples obtained using zein, and from 20 μm to 3 mm for samples obtained by foaming in a carbon dioxide medium. The SEM images demonstrated the macro- and mesoporous fibrous structure of the obtained materials. The nitrogen porosimetry results indicated that samples obtained using surfactants and zein are characterized by a high specific surface area (592–673 m²/g), comparable to the specific surface area for an alginate-based aerogel obtained without the use of pore-forming components. However, the use of the developed methods for the formation of a hierarchical porous structure contributes to an increase in the specific mesopores volume (up to 17.7 cm³/g). The materials obtained by foaming in a carbon dioxide medium are characterized by lower specific surface areas (112–239 m²/g) and specific mesopores volumes (0.6–2.1 cm³/g). Thus, this paper presents a set of methods for forming hierarchical porous structures that can obtain delivery systems for active substances with a controlled release profile and highly efficient platforms for cell culturing. Full article

Polymers with micro- and mesoporous structure are promising as materials for gas storage and separation, encapsulating agents for controlled drug release, carriers for catalysts and sensors, precursors of nanostructured carbon materials, carriers for biomolecular immobilization and cellular scaffolds, as materials with a low dielectric constant, filtering/separating membranes, proton exchange membranes, templates for replicating structures, and as electrode materials for energy storage. Sol–gel technologies, track etching, and template synthesis are used for their production, including in micelles of surfactants and microemulsions and sublimation drying. The listed methods make it possible to obtain pores with variable shapes and sizes of 5–50 nm and achieve a narrow pore size distribution. However, all these methods are technologically multi-stage and require the use of consumables. This paper presents a review of the use of macromolecular architecture in the synthesis of micro- and mesoporous polymers with extremely high surface area and hierarchical porous polymers. The synthesis of porous polymer frameworks with individual functional capabilities, the required chemical structure, and pore surface sizes is based on the unique possibilities of developing the architecture of the polymer matrix. Full article