Search Results (86)

Biochar, a porous carbonaceous material derived from the pyrolysis of biomass under oxygen-limited conditions, offers several advantages for environmental remediation, including a high specific surface area, ease of preparation, and abundant raw material sources. However, the application of pristine biochar is limited by its inherent physicochemical shortcomings, such as a lack of active functional groups and limited elemental compositions. To overcome these limitations, metal-modified biochars have garnered increasing attention. In particular, iron-manganese (Fe-Mn) modification significantly enhances the adsorption capacity, redox potential, and microbial activity of biochar, owing to the synergistic interactions between Fe and Mn. Iron-manganese-modified biochar (FM-BC) has demonstrated effective removal of heavy metals, organic matter, phosphate, and nitrate through mechanisms including mesoporous adsorption, redox reactions, complexation, electrostatic interactions, and precipitation. Moreover, FM-BC can improve soil physicochemical properties and support plant growth, highlighting its promising potential for broader environmental application. This review summarizes the preparation methods, environmental remediation mechanisms, and practical applications of FM-BC and discusses future directions in mechanism elucidation, biomass selection, and engineering implementation. Overall, FM-BC, with its tunable properties and multifunctional capabilities, emerges as a promising and efficient material for addressing complex environmental pollution challenges. Full article

This study presents research on the production of activated biocarbons derived from herbal waste. Sage stems were chemically activated with two activating agents of different chemical natures—H₃PO₄ and K₂CO₃—and subjected to two thermal treatment methods: conventional and microwave heating. The effect of the activating agent type and heating method on the basic physicochemical properties of the resulting activated biocarbons was investigated. These properties included surface morphology, elemental composition, ash content, pH of aqueous extracts, the content and nature of surface functional groups, points of zero charge, and isoelectric points, as well as the type of porous structure formed. In addition, the potential of the prepared carbonaceous materials as adsorbents of model organic (represented by Triton X-100 and methylene blue) and inorganic (represented by iodine) pollutants was assessed. The influence of the initial adsorbate concentration (5–150 (dye) and 10–800 mg/dm³ (surfactant)), temperature (20–40 °C), and pH (2–10) of the system on the efficiency of contaminant removal from aqueous solutions was evaluated. The adsorption kinetics were also investigated to better understand the rate and mechanism of contaminant uptake by the prepared activated biocarbons. The results showed that materials activated with orthophosphoric acid exhibited a significantly higher sorption capacity for all tested adsorbates compared to their potassium carbonate-activated counterparts. Microwave heating was found to be more effective in promoting the formation of a well-developed specific surface area (471–1151 m²/g) and porous structure (mean pore size 2.17–3.84 nm), which directly enhanced the sorption capacity of both organic and inorganic contaminants. The maximum adsorption capacities for iodine, methylene blue, and Triton X-100 reached the levels of 927.0, 298.4, and 644.3 mg/g, respectively, on the surface of the H₃PO₄-activated sample obtained by microwave heating. It was confirmed that the heating method used during the activation step plays a key role in determining the physicochemical properties and sorption efficiency of activated biocarbons. Full article

This study focuses on the production and characterization of activated carbons derived from the carbonaceous residue obtained through the catalytic pyrolysis of waste tires. A catalytic pyrolysis process was conducted at 450 °C and 575 °C, employing two zeolitic catalysts, the commercial ZSM-5 and a synthesized zeolite (PZ2), developed from natural pozzolan, which played a key role in the pyrolysis performance and the quality of the resulting carbons. After pyrolysis, the solid residues were chemically activated using KOH to improve their porous structure and surface characteristics. Comprehensive characterization was carried out, including textural properties (BET surface area and porosity) and morphological (SEM) analysis of the activated carbons, as well as crystallinity evaluation (XRD) of the zeolitic catalysts. The BET surface areas of activated carbons PZ2-T1-AK and PZ2-T2-AK reached 608.65 m²/g and 624.37 m²/g, respectively, values that surpass those reported for similar materials under comparable activation conditions. The developed porous structure suggests strong potential for applications in adsorption processes, including pollutant removal. These findings demonstrate the effectiveness of zeolite-catalyzed pyrolysis, particularly using PZ2, as a sustainable strategy for transforming tire waste into high-performance adsorbent materials. This approach supports circular economy principles through innovative waste valorization and offers a promising solution to an environmental challenge. Full article

This study systematically investigates the combustion behavior and kinetic characteristics of oil shale semi-coke. Thermogravimetric analysis (TGA) experiments, combined with both model-free and model-based methods, were used to explore the thermal characteristics, kinetic parameters, and reaction mechanisms of the combustion process. The results show that the combustion process of oil shale semi-coke can be divided into three stages: a low-temperature stage (50–310 °C), a mid-temperature stage (310–670 °C), and a high-temperature stage (670–950 °C). The mid-temperature stage is the core of the combustion process, accounting for approximately 28–37% of the total mass loss, with the released energy concentrated and exhibiting significant thermal chemical activity. Kinetic parameters calculated using the model-free methods (OFW and KAS) and the model-based Coats–Redfern method reveal that the activation energy gradually increases with the conversion rate, indicating a multi-step reaction characteristic of the combustion process. The F2-R3-F2 model, with its segmented mechanism (boundary layer + second-order reaction), better fits the physicochemical changes during semi-coke combustion, and the analysis of mineral phase transformations is more reasonable. Therefore, the F2-R3-F2 model is identified as the optimal model in this study and provides a scientific basis for the optimization of oil shale semi-coke combustion processes. Furthermore, scanning electron microscopy (SEM) and X-ray diffraction (XRD) analyses were conducted on oil shale semi-coke samples before and after combustion to study the changes in the combustion residues. SEM images show that after combustion, the surface of the semi-coke sample exhibits a large number of irregular holes, with increased pore size and a honeycomb-like structure, indicating that the carbonaceous components were oxidized and decomposed during combustion, forming a porous structure. XRD analysis shows that the characteristic peaks of quartz (Q) are enhanced after combustion, while those of calcite (C) and pyrite (P) are weakened, suggesting that the mineral components underwent decomposition and transformation during combustion, particularly the decomposition of calcite into CO₂ at high temperatures. Infrared spectroscopy (IR) analysis reveals that after combustion, the amount of hydrocarbons in the semi-coke decreases, while aromatic compounds and incompletely decomposed organic materials are retained, further confirming the changes in organic matter during combustion. Full article

Water pollution from industrial, municipal, and agricultural sources is a pressing global concern, necessitating the development of sustainable and efficient treatment solutions. Algal biomass has emerged as a promising feedstock for the production of carbonaceous adsorbents due to its rapid growth, high photosynthetic efficiency, and ability to thrive in wastewater. This review examines the conversion of algal biomass into biochar and hydrochar through pyrolysis and hydrothermal processes, respectively, and evaluates their potential applications in wastewater treatment, carbon sequestration, and biofuel production. Pyrolyzed algal biochars typically exhibit a moderate to high carbon content and a porous structure but require activation treatments (e.g., KOH or ZnCl₂) to enhance their surface area and adsorption capabilities. Hydrothermal carbonization, conducted at lower temperatures (180–260 °C), produces hydrochars rich in oxygenated functional groups with enhanced cation exchange capacities, making them effective for pollutant removal. Algal-derived biochars and hydrochars have been successfully applied for the adsorption of heavy metals, dyes, and pharmaceutical contaminants, with adsorption capacities significantly increasing through post-treatment modifications. Beyond wastewater treatment, algal biochars serve as effective carbon sequestration materials due to their stable structure and high carbon retention. Their application as soil amendments enhances long-term carbon storage and improves soil fertility. Additionally, algal biomass plays a key role in biofuel production, particularly for biodiesel synthesis, where microalgae’s high lipid content facilitates bio-oil generation. Hydrochars, with energy values in the range of 20–26 MJ/kg, are viable solid fuels for combustion and co-firing, supporting renewable energy generation. Furthermore, the integration of these materials into bioenergy systems allows for waste valorization, pollution control, and energy recovery, contributing to a sustainable circular economy. This review provides a comprehensive analysis of algal-derived biochars and hydrochars, emphasizing their physicochemical properties, adsorption performance, and post-treatment modifications. It explores their feasibility for large-scale wastewater remediation, carbon capture, and bioenergy applications, addressing current challenges and future research directions. By advancing the understanding of algal biomass as a multifunctional resource, this study highlights its potential for environmental sustainability and energy innovation. Full article

This paper investigates the use of spent tyre rubber as a precursor for synthesising adsorbents to recover rare earth elements. Through pyrolysis and CO₂ activation, tyre rubber is converted into porous carbonaceous materials with surface properties suited for rare earth element adsorption. The study also examines the efficiency of leaching rare earth elements from NdFeB magnets using optimised acid leaching methods, providing insights into recovery processes. The adsorption capacity of the materials was assessed through batch adsorption assays targeting neodymium (Nd³⁺) and dysprosium (Dy³⁺) ions. Results highlight the superior performance of activated carbon derived from tyre rubber following CO₂ activation, with the best-performing adsorbent achieving maximum uptake capacities of 24.7 mg·g⁻¹ for Nd³⁺ and 34.4 mg·g⁻¹ for Dy³⁺. Column studies revealed efficient adsorption of Nd³⁺ and Dy³⁺ from synthetic and real magnet leachates with a maximum uptake capacity of 1.36 mg·g⁻¹ for Nd³⁺ in real leachates and breakthrough times of 25 min. Bi-component assays showed no adverse effects when both ions were present, supporting their potential for simultaneous recovery. Furthermore, the adsorbents effectively recovered rare earth elements from e-waste magnet leachates, demonstrating practical applicability. This research underscores the potential of tyre rubber-derived adsorbents to enhance sustainability in critical raw material supply chains. By repurposing waste tyre rubber, these materials offer a sustainable solution for rare earth recovery, addressing resource scarcity while aligning with circular economy principles by diverting waste from landfills and creating value-added products. Full article

Si anode materials are promising candidates for next-generation Li-ion batteries (LIBs) because of their high capacities. However, expansion and low conductivity result in rapid performance degradation. Herein, we present a facile one-pot method for pyrolyzing polystyrene sulfonate (PSS) polymers at low temperatures (≤400 °C) to form a thin carbonaceous layer on the silicon surface. Specifically, micron silicon (mSi) was transformed into porous mSi (por-mSi) by a metal-assisted chemical etching method, and a phenyl-based thin film derived from the thermolysis of PSS formed a strong Si–C/Si–O–C covalent bonding with the Si surface, which helped maintain stable cycle performance by improving the interfacial properties of mSi. Additionally, PSS-grafted por-mSi (por-mSi@PSS) anode was coated with polyaniline (PANI) for endowing additional electrical conductivity. The por-mSi@PSS/PANI anode demonstrated a high reversible capacity of ~1500 mAh g⁻¹ at 0.1 A g⁻¹ after 100 cycles, outperforming or matching the performance reported in recent studies. A thin double layer composed of phenyl moieties and a conductive PANI coating improved the stability of Si-based anodes and provided an effective pathway for Li⁺ ion transport to the Si interface, suggesting that polymer-modified Si anodes hold significant promise for advanced LIB applications. Full article

The presence of pharmaceuticals in aquatic ecosystems is an issue of increasing concern. Regardless of the low concentration of pharmaceuticals in water, they can have a toxic effect on both humans and aquatic organisms. Advanced oxidation processes (AOPs) have been described as a promising technique for eliminating pharmaceuticals due to their high efficiency. However, the cost associated with the application of these processes and their high reagents and energy requirements have affected the implementation of AOPs at large scales. Biochar has been suggested to be used as a catalyst in AOPs to overcome these limitations. Biochar is considered as an alternative heterogeneous catalyst thanks to its physicochemical characteristics like its specific surface area, porous structure, oxygen-containing functional groups, electrical conductivity, persistent free radicals (PFRs), modifiable properties, and structure defects. This carbonaceous material presents the capacity to activate oxidizing agents leading to the formation of radical species, which are needed to degrade pharmaceuticals. Additionally, AOP/biochar systems can destroy pharmaceutical molecules following a non-radical pathway. To enhance biochar catalytic performance, modifications have been suggested such as iron (Fe) impregnation, heteroatom doping, and supporting semiconductors on the biochar surface. Although biochar has been efficiently used in combination with several AOPs for the mineralization of pharmaceuticals from water, further research must be conducted to evaluate different regeneration techniques to increase biochar’s sustainable applicability and reduce the operational cost of the combined process. Moreover, operational conditions influencing the combined system are required to be evaluated to discern their effect and find conditions that maximize the degradation of pharmaceuticals by AOP/biochar systems. Full article

It is difficult for carbonaceous materials to combine a large specific surface area with flexibility. Here, a flexible all-carbon nanoarchitecture based on the in situ growth of nanoporous graphene within “skeletal-capillary” carbon nanotube (CNT) networks has been achieved by a chemical vapor deposition (CVD) process. Multi-path long-range conductivity is established, and the porous graphene provides a large specific surface area for charge storage. The flexibility of the films allows them to be directly used as binder-free electrodes for supercapacitors. Since the polymeric binders are saved, the supercapacitors exhibit a higher overall storage density. Full article

Hierarchical porous carbon derived from discarded biomass for energy storage materials has attracted increasing research attention due to its cost-effectiveness, ease of fabrication, environmental protection, and sustainability. Brewed tea leaves are rich in heteroatoms that are beneficial to capacitive energy storage behavior. Therefore, we synthesized high electrochemical performance carbon-based composites from Tie guan yin tea leaf waste using a facile procedure comprising hydrothermal, chemical activation, and calcination processes. In particular, potassium permanganate (KMnO₄) was incorporated into the potassium hydroxide (KOH) activation agent; therefore, during the activation process, KOH continued to erode the biomass precursor, producing abundant pores, and KMnO₄ synchronously underwent a redox reaction to form MnO nanoparticles and anchor on the porous carbon through chemical bonding. MnO nanoparticles provided additional pseudocapacitive charge storage capabilities through redox reactions. The results show that the amount of MnO produced is proportional to the amount of KMnO₄ incorporated. However, the specific surface area of the composite material decreases with the incorporated amount of KMnO₄ due to the accumulation and aggregation of MnO nanoparticles, thereby even blocking some micropores. Optimization of MnO nanocrystal loading can promote the crystallinity and graphitization degree of carbonaceous materials. The specimen prepared with a weight ratio of KMnO₄ to hydrochar of 0.02 exhibited a high capacitance of 337 F/g, an increase of 70%, owing to the synergistic effect between the Tie guan yin tea leaf-derived activated carbon and MnO nanoparticles. With this facile preparation method and the resulting high electrochemical performance, the development of manganese oxide/carbon composites derived from tea leaf biomass is expected to become a promising candidate as an energy storage material for supercapacitors. Full article

Hydrochar, an attractive member of the carbonaceous materials, is derived from biomass and projects great potential in peroxymonosulfate (PMS) activation, but has not been studied much. Herein, by using the large-scale cultured Chlorella vulgaris and field-collected bloom algae, a series of porous hydrochar was synthesized via a facile hydrothermal carbonization reaction, while Co doping significantly increased their specific surface areas, carbonization degree, and surface functional groups. These Co-doped hydrochar (xCo-HC, x: amount of the Co precursor) could efficiently activate the PMS, resulting in nearly 100% removal of five common paraben pollutants within 40 min. A dosage of 0.2Co-HC of 0.15 g/L, a PMS concentration of 0.6 g/L, and an unadjusted pH of 6.4 were verified more appropriately for paraben degradation. The coexistence of Cl⁻, SO₄²⁻, and humic acid inhibited the degradation, while HCO₃⁻ showed an enhancing effect. No observable change was found at the presence of NO₃⁻. Quenching results illustrated that the produced •SO₄⁻ during the conversion of doped Co³⁺/Co²⁺ acted as the dominant active species for paraben degradation, while •O₂⁻, ¹O₂, and •OH contributed relatively less. The algae-based hydrochar potentially facilitated the electron transfer in the xCo-HC/PMS system. Overall, this study develops a new strategy for resource utilization of the abundant algae. Full article

Vertically ordered mesoporous silica films (VMSF) are a class of porous materials composed of ultrasmall pores and ultrathin perpendicular nanochannels, which are attractive in the areas of electroanalytical sensors and molecular separation. However, VMSF easily falls off from the carbonaceous electrodes and thereby impacts their broad applications. Herein, carbon nitride nanosheets (CNNS) were served as an adhesive layer for stable growth of VMSF on the glassy carbon electrode (GCE). CNNS bearing plentiful oxygen-containing groups can covalently bind with silanol groups of VMSF, effectively promoting the stability of VMSF on the GCE surface. Benefiting from numerous open nanopores of VMSF, modification of VMSF’s external surface with carbohydrate antigen 15-3 (CA15-3)-specific antibody allows the target-controlled transport of electrochemical probes through the internal silica nanochannels, yielding sensitive quantitative detection of CA15-3 with a broad detection range of 1 mU/mL to 1000 U/mL and a low limit of detection of 0.47 mU/mL. Furthermore, the proposed VMSF/CNNS/GCE immunosensor is capable of highly selective and accurate determination of CA15-3 in spiked serum samples, which offers a simple and effective electrochemical strategy for detection of various practical biomarkers in complicated biological specimens. Full article

In the chemical industry and in the manufacturing sector, the adsorption properties of porous materials have been proven to be of great interest for the removal of impurities from liquid and gas media. While it is acknowledged that significant progress and literature production have been developed in this field, there have been adsorption studies that failed to further advance our knowledge in generating a better understanding of the prevailing sorption types and dominant adsorption processes. Therefore, this review study has focused on porous materials, their sorption types and their adsorption properties, further investigating the adsorption properties of porous materials at either solid–gas and solid–liquid interfaces, underscoring both the properties of the materials, the characterization and the correlation between the porosity and the adsorption capacity, as well as the emergent interactions between the adsorbent and adsorbate molecules, including the adsorption mechanisms, the types of sorption and the kinetic and thermodynamic information conveyed. Full article

The formation of chondrite materials represents one of the earliest mineralogical processes in the solar system. Phyllosilicates are encountered at various stages of the chondrule formation, from the initial stages (IDP agglomerates) to the final steps (chondrule internal alteration). While typically linked to aqueous alteration, recent studies reveal that phyllosilicates could precipitate directly from residual fluids in post-magmatic or deuteric conditions and under a wide range of temperatures, pressures, water/rock ratios, and H₂/H₂O ratio conditions. This study re-examined the formation of hydrated phyllosilicates in chondrules and associated fine-grained rims (FGRs) using published petrographical, mineralogical, and chemical data on carbonaceous chondrites. Given that chondrules originate from the melting of interplanetary dust particles, the water liberated by the devolatilization of primary phyllosilicates, including clay minerals or ice melting, reduces the melting temperature and leads to water dissolution into the silicate melt. Anhydrous minerals (e.g., olivine and diopside) form first, while volatile and incompatible components are concentrated in the residual liquid, diffusing into the matrix and forming less porous FGRs. Serpentine and cronstedtite are the products of thermal metamorphic-like mineral reactions. The mesostasis in some lobated chondrules is composed of anhydrous and hydrous minerals, i.e., diopside and serpentine. The latter is probably not the alteration product of a glassy precursor but rather a symplectite component (concomitant crystallization of diopside and serpentine). If so, the symplectite has been formed at the end of the cooling process (eutectic-like petrographical features). Water trapped inside chondrule porosity can lead to the local replacement of olivine by serpentine without external water input (auto-alteration). In the absence of water, hydrated phyllosilicates do not crystallize, forming a different mineral assemblage. Full article

Selective oxidation, which is crucial in diverse chemical industries, transforms harmful chemicals into valuable compounds. Heterogeneous sonocatalysis, an emerging sustainable approach, urges in-depth exploration. In this work, we investigated N-doped or non-doped carbonaceous materials as alternatives to scarce, economically sensitive metal-based catalysts. Having synthesized diverse carbons using a hard-template technique, we subjected them to sonication at frequencies of 22, 100, 500, and 800 kHz with a 50% amplitude. Sonochemical reaction catalytic tests considerably increased the catalytic activity of C-meso (non-doped mesoporous carbon material). The scavenger test showed a radical formation when this catalyst was used. N-doped carbons did not show adequate and consistent sonoactivity for the selective oxidation of 4-Hydroxy-3,5 dimethoxybenzyl alcohol in comparison with control conditions without sonication, which might be associated with an acid–base interaction between the catalysts and the substrate and sonoactivity prohibition by piridinic nitrogen in N-doped catalysts. Full article