Search Results (410)

Biochar, a carbon-rich material derived from biomass, presents a sustainable solution to several pressing challenges in U.S. agriculture, including soil degradation, carbon emissions, and waste management. Despite global advancements, the U.S. biochar market remains underexplored in terms of economic viability, adoption potential, and sector-specific applications. This narrative review synthesizes two decades of literature to examine biochar’s applications, production methods, and market dynamics, with a focus on its economic and environmental role within the United States. The review identifies biochar’s multifunctional benefits: enhancing soil fertility and crop productivity, sequestering carbon, reducing greenhouse gas emissions, and improving water quality. Recent empirical studies also highlight biochar’s economic feasibility across global contexts, with yield increases of up to 294% and net returns exceeding USD 5000 per hectare in optimized systems. Economically, the global biochar market grew from USD 156.4 million in 2021 to USD 610.3 million in 2023, with U.S. production reaching ~50,000 metric tons annually and a market value of USD 203.4 million in 2022. Forecasts project U.S. market growth at a CAGR of 11.3%, reaching USD 478.5 million by 2030. California leads domestic adoption due to favorable policy and biomass availability. However, barriers such as inconsistent quality standards, limited awareness, high costs, and policy gaps constrain growth. This study goes beyond the existing literature by integrating market analysis, SWOT assessment, cost–benefit findings, and production technologies to highlight strategies for scaling biochar adoption. It concludes that with supportive legislation, investment in research, and enhanced supply chain transparency, biochar could become a pivotal tool for sustainable development in the U.S. agricultural and environmental sectors. Full article

Hydrogen is widely recognized as a key enabler of the clean energy transition, but the lack of safe, efficient, and scalable storage technologies continues to hinder its broad deployment. Conventional hydrogen storage approaches, such as compressed hydrogen storage, cryo-compressed hydrogen storage, and liquid hydrogen storage, face limitations, including high energy consumption, elevated cost, weight, and safety concerns. In contrast, solid-state hydrogen storage using carbon-based adsorbents has gained growing attention due to their chemical tunability, low cost, and potential for modular integration into energy systems. This review provides a comprehensive evaluation of hydrogen storage using carbon-based materials, covering fundamental adsorption mechanisms, classical materials, emerging architectures, and recent advances in computationally AI-guided material design. We first discuss the physicochemical principles driving hydrogen physisorption, chemisorption, Kubas interaction, and spillover effects on carbon surfaces. Classical adsorbents, such as activated carbon, carbon nanotubes, graphene, carbon dots, and biochar, are evaluated in terms of pore structure, dopant effects, and uptake capacity. The review then highlights recent progress in advanced carbon architectures, such as MXenes, three-dimensional architectures, and 3D-printed carbon platforms, with emphasis on their gravimetric and volumetric performance under practical conditions. Importantly, this review introduces a forward-looking perspective on the application of artificial intelligence and machine learning tools for data-driven sorbent design. These methods enable high-throughput screening of materials, prediction of performance metrics, and identification of structure–property relationships. By combining experimental insights with computational advances, carbon-based hydrogen storage platforms are expected to play a pivotal role in the next generation of energy storage systems. The paper concludes with a discussion on remaining challenges, utilization scenarios, and the need for interdisciplinary efforts to realize practical applications. Full article

Gasification of municipal solid waste and other biogenic residues (e.g., biomass and biowaste) is increasingly recognized as a promising thermochemical pathway for converting non-recyclable fractions into valuable energy carriers, with applications in electricity generation, district heating, hydrogen production, and synthetic fuels. This paper provides a comprehensive analysis of major gasification technologies, including fixed bed, fluidized bed, entrained flow, plasma, supercritical water, microwave-assisted, high-temperature steam, and rotary kiln systems. Key aspects such as feedstock compatibility, operating parameters, technology readiness level, and integration within circular economy frameworks are critically evaluated. A comparative assessment of incineration and pyrolysis highlights the environmental and energetic advantages of gasification. The valorization pathways for main product (syngas) and by-products (syngas, ash, tar, and biochar) are also explored, emphasizing their reuse in environmental, agricultural, and industrial applications. Despite progress, large-scale adoption in Europe is constrained by economic, legislative, and technical barriers. Future research should prioritize scaling emerging systems, optimizing by-product recovery, and improving integration with carbon capture and circular energy infrastructures. Supported by recent European policy frameworks, gasification is positioned to play a key role in sustainable waste-to-energy strategies, biomass valorization, and the transition to a low-emission economy. Full article

Soil acidification, salinization, and heavy metal pollution pose serious threats to global food security and sustainable agricultural development. Biochar, with its high porosity, large surface area, and abundant functional groups, can effectively improve soil properties. However, due to variations in feedstocks and pyrolysis conditions, it may contain potentially harmful substances. Industrial wastes such as fly ash, steel slag, red mud, and phosphogypsum are rich in minerals and show potential for soil improvement, but direct application may pose environmental risks. The co-application of biochar with these wastes can produce composite amendments that enhance pH buffering capacity, nutrient availability, and pollutant immobilization. Therefore, a review of biochar-industrial waste composites as soil amendments is crucial for addressing soil degradation and promoting resource utilization of wastes. In this study, the literature was retrieved from Web of Science, Scopus, and Google Scholar using keywords including biochar, fly ash, steel slag, red mud, phosphogypsum, combined application, and soil amendment. A total of 144 articles from 2000 to 2025 were analyzed. This review summarizes the physicochemical properties of biochar and representative industrial wastes, including pH, electrical conductivity, surface area, and elemental composition. It examines their synergistic mechanisms in reducing heavy metal release through adsorption, complexation, and ion exchange. Furthermore, it evaluates the effects of these composites on soil health and crop productivity, showing improvements in soil structure, nutrient balance, enzyme activity, and metal immobilization. Finally, it identifies knowledge gaps as well as future prospects and recommends long-term field trials and digital agriculture technologies to support the sustainable application of these composites in soil management. Full article

The construction sector makes a major contribution to global greenhouse gas emissions, in which cement alone produces approximately 7–8% of global CO₂ emissions. To abate environmental impact and promote sustainable construction, alternative low-carbon cementitious materials are gaining attention. Biochar (BC), a carbon-rich material obtained from biomass sources through the process of pyrolysis, has surfaced as a capable supplementary cementitious material due to its carbon capture capabilities and positive impact on the characteristics of cement composites. This review investigates the role of BC in cement composites, including its effects on hydration kinetics, microstructural development, fresh-state properties, and its optimal utilisation. The study also highlights the internal curing capabilities of BC when used in cement composites, its role in promoting hydration product formation, and its dual function in enhancing mechanical performance while facilitating carbon capture. Despite the benefits, there are some challenges such as variable BC properties, optimal dosage, and scalability. The review highlights the need for standardisation and further research to fully harness BC’s potential as a sustainable component in low-carbon construction technologies. Full article

This study investigated the degradation efficacy, kinetics, and mechanism of the ozone (O₃) process and two enhanced O₃ processes (O₃/peroxymonosulfate (O₃/PMS) and O₃/peroxymonosulfate/iron molybdates/biochar composite (O₃/PMS/FeMoBC)), especially the O₃/PMS/FeMoBC process, for the degradation of tetracycline (TC) in water. An FeMoBC sample was synthesized by the impregnation–pyrolysis method. The XRD results showed that the material loaded on BC was an iron molybdates composite, in which Fe₂Mo₃O₈ and FeMoO₄ accounted for 26.3% and 73.7% of the composite, respectively. The experiments showed that, for the O₃/PMS/FeMoBC process, the optimum conditions were obtained at pH 6.8 ± 0.1, an initial concentration of TC of 0.03 mM, an FeMoBC dosage set at 200 mg/L, a gaseous O₃ concentration set at 3.6 mg/L, and a PMS concentration set at 30 μM. Under these reaction conditions, the degradation rate of TC in 8 min and 14 min reached 94.3% and 98.6%, respectively, and the TC could be reduced below the detection limit (10 μg/L) after 20 min of reaction. After recycling for five times, the degradation rate of TC could still reach about 40%. The introduction of FeMoBC into the O₃/PMS system significantly improved the TC degradation efficacy and resistance to inorganic anion interference. Meanwhile, it enhanced the generation of hydroxyl radicals (^•OH) and sulfate radicals (SO₄^•−), thus improving the oxidizing efficiency of TC in water. Material characterization analysis showed that FeMoBC has a well-developed porous structure and abundant active sites, which is beneficial for the degradation of pollutants. The reaction mechanism of the O₃/PMS/FeMoBC system was speculated by the EPR technique and quenching experiments. The results showed that FeMoBC efficiently catalyzed the O₃/PMS process to generate a variety of reactive oxygen species, leading to the efficient degradation of TC. There are four active oxidants in O₃/PMS/FeMoBC system, namely ^•OH, SO₄^•−, ¹O₂, and •O₂⁻. The order of their contribution importance was ^•OH, ¹O₂, SO₄^•−, and •O₂⁻. This study provides an effective technological pathway for the removal of refractory organic matter in the aquatic environment. Full article

The combined application of chemical fertilizers with organic materials contributes to higher contents of bioavailable phosphorus. However, the underlying mechanism remains poorly understood. A field experiment including four treatments, chemical fertilizer (CF), chemical fertilizer with biochar (CB), chemical fertilizer with organic fertilizer (CO), and chemical fertilizer with biochar and organic fertilizer (CBO), was conducted to explore how the combination of fertilizer applications enhanced soil phosphorus bioavailability using metagenomic sequencing technology. The results showed that chemical fertilizers combined with organic materials (CB, CO, and CBO) significantly increased citrate-extractable phosphorus by 34.61–138.92% and hydrochloric acid-extractable phosphorus contents by 72.85–131.07% compared to CF. In addition, the combined applications altered the microbial community structure and increased the abundance of phoR, spoT, and ppnK genes, but decreased those of gcd, phoD, and ppk1 genes. A partial least squares path model indicated that the combined applications regulated the microbial community composition and gene abundance of phosphorus-cycling microorganisms by influencing soil physicochemical properties, thereby enhancing soil phosphorus cycling. Correlation analysis indicated that pH, total phosphorus, and available phosphorus were the key factors influencing microbial communities, while available nitrogen and total nitrogen primarily regulated phosphorus cycling gene abundance. In addition, the CO and CBO treatments significantly increased maize yield by 14.60% and 21.04%, respectively. Overall, CBO most effectively enhanced bioavailable phosphorus content and maize yield. This study provides a foundation for developing rational fertilization strategies and improving soil phosphorus use efficiency. Full article

This study investigates the synthesis of highly porous ZnCl₂-activated biochars derived from sawdust through controlled pyrolysis at 300 °C and 500 °C, aiming to enhance CO₂ adsorption performance. The effects of pyrolysis temperature and chemical activation on particle size distribution, surface area, and pore structure are systematically analyzed. Particle size analysis reveals that higher pyrolysis temperature and ZnCl₂ activation significantly reduce both median and mean particle sizes, resulting in finer and more uniform biochar morphology. BET analysis demonstrates a substantial increase in specific surface area and micropore volume upon ZnCl₂ activation, particularly at 500 °C, where the activated biochar (S500ZC) exhibits a high surface area of 717.60 m²/g and a micropore area of 616.60 m²/g. CO₂ adsorption isotherms recorded at 25 °C confirm that both thermal treatment and activation markedly enhance adsorption capacity, with the highest uptake of 35.34 cm³/g achieved by S500ZC. The adsorption performance follows the order: S300NZC < S300ZC < S500NZC < S500ZC, closely correlating with microporosity and surface textural development. The findings highlight the potential of ZnCl₂-activated biochars as cost-effective, environmentally friendly, and efficient sorbents for scalable CO₂ mitigation technologies. Full article

The disposal of wastewater resulting from petroleum industries presents a major environmental challenge due to the presence of hard-to-degrade organic pollutants, such as oils and hydrocarbons, and high chemical oxygen demand (COD). In this study, an efficient and eco-friendly method was developed to treat such wastewater using a photocatalyst composed of biochar derived from pistachio shells and loaded with zinc oxide (ZnO) nanoparticles. The biochar-ZnO composite was prepared via a co-precipitation-assisted pyrolysis method to evaluate its efficiency in the photocatalytic degradation of petroleum wastewater (PW). The synthesized material was characterized using various techniques, including scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier transform infrared (FTIR) spectroscopy, to determine surface morphology, crystal structure, and functional groups present on the catalyst surface. Photocatalytic degradation experiments were conducted under UV and sunlight for 90 h of irradiation to evaluate the performance of the proposed system in removing oil and reducing COD levels. Key operational parameters, such as pH (2–10), catalyst dosage (0–0.1) g/50 mL, and oil and COD concentrations (50–500) ppm and (125–1252) ppm, were optimized by response surface methodology (RSM) to obtain the maximum oil and COD removal efficiency. The oil and COD were removed from PW (90.20% and 88.80%) at 0.1 g/50 mL of PS/ZnO, a pH of 2, and 50 ppm oil concentration (125 ppm of COD concentration) under UV light. The results show that pollutant removal is slightly better when using sunlight (80.00% oil removal, 78.28% COD removal) than when using four lamps of UV light (77.50% oil removal, 75.52% COD removal) at 0.055 g/50 mL of PS/ZnO, a pH of 6.8, and 100 ppm of oil concentration (290 ppm of COD concentration). The degradation rates of the PS/ZnO supported a pseudo-first-order kinetic model with R² values of 0.9960 and 0.9922 for oil and COD. This work indicates the potential use of agricultural waste, such as pistachio shells, as a sustainable source for producing effective catalysts for industrial wastewater treatment, opening broad prospects in the field of green and nanotechnology-based environmental solutions in the development of eco-friendly and effective wastewater treatment technologies under solar light. Full article

The sludge pyrolysis technology for biochar production delivers dual environmental benefits, addressing both sludge disposal challenges and enabling environmental remediation through the utilization of the resultant biochar. However, the complex multi-step procedures and low catalyst output in previous studies constrain the practical implementation of this technology. A facile sludge pyrolysis method was constructed to achieve the batch production of municipal sludge biochar (MSB) in this study. Compared to municipal sludge (MS), the resultant MSB showed a higher BET surface area, more well-developed pore channel architecture, and plentiful active sites for activating peroxymonosulfate (PMS). Under the optimized conditions (C_MSB = C_PMS = 0.2 g/L), 93.34% of Acid Red G (ARG, 20 mg/L) was degraded after 10 min, posing an excellent rate constant of 0.278 min⁻¹. Additionally, MSB demonstrated excellent broad pH adaptability, ion interference resistance, reusability, and recyclability for ARG elimination. It was primary Fe sites that excited PMS to generate ${\mathrm{O}}_2^{•-}$ and Fe-oxo species (Fe^IV=O) for ARG degradation. The reaction process exhibited minimal heavy metal leaching, indicating limited environmental risk. Therefore, the practical applicability of the sludge biochar production, coupled with its scalable manufacturing capacity and exceptional catalytic activity, collectively demonstrated that this study established a viable pyrolysis methodology for municipal sludge, offering critical insights for sludge disposal and resource reutilization. Full article

Biochar-based adsorbents synthesized from agricultural wastes have emerged as economical and environmentally sustainable materials for water purification. In this study, coffee shell-derived biochars were synthesized via pyrolysis at 500 and 700 °C, with and without water washing, and comprehensively characterized to evaluate their potential for removing Rhodamine B (RhB) from aqueous solution. Structural and surface analyses indicated that a higher pyrolysis temperature enhanced pore development and aromaticity, whereas water washing effectively removed inorganic ash, thereby exposing additional active sites. Among all samples, water-washed biochar pyrolyzed at 700 °C (WCB700) exhibited the highest surface area (273.6 m²/g) and adsorption capacity (193.5 mg/g). The adsorption kinetics conformed to a pseudo-second-order model, indicating chemisorption, and the equilibrium data fit the Langmuir model, suggesting monolayer coverage. Mechanism analysis highlighted the roles of π–π stacking, hydrogen bonding, electrostatic interaction, and pore filling. Additionally, WCB700 retained more than 85% of its original capacity after five regeneration cycles, demonstrating excellent stability and reusability. This study presents an economical approach to valorizing coffee waste as well as provides mechanistic insights into optimizing biochar surface chemistry for enhanced dye removal. These findings support the application of engineered biochar in scalable and sustainable wastewater treatment technologies. Full article

A core tertiary wastewater reactive filtration technology, where continuously renewed hydrous ferric oxide coated sand is created in an upflow continuous backwash filter, has been adopted in about 100 water resource recovery facilities in several countries. Primarily focused on ultralow phosphorus discharge requirements to address nutrient pollution impacts and harmful algae blooms, the technology has also demonstrated the capacity to address high-efficiency removals of Hg, As, Zn, N, and other pollutants of concern, in addition to water quality needs met by common sand filtration, including total suspended solids. Recent work has demonstrated the capability of an additive iron–ozone catalytic oxidation process to the core reactive filtration technology platform to address micropollutants such as pharmaceuticals. Most recently, direct injection of frangible biochar into the reactive sand filter bed as a consumable reagent demonstrates a novel biochar water treatment technology in a platform that yields dose-dependent carbon negativity. In this work, the reactive filtration technology performance is reviewed from field pilot-scale to full-scale installation scenarios for nutrient removal and recovery applications. We also review the potential of the technology for nutrient recovery with the addition of biochar and micropollutant destructive removal with catalytic oxidation. Research exploration of this reactive filtration technology includes life cycle assessment (LCA) and techno-economic assessment to evaluate the environmental and economic impacts of this advanced water treatment technology. A recent LCA study of a pilot-scale field research and full-scale municipal system with over 2200 inventory elements shows a dose-dependent carbon negativity when biochar is injected into the process stream of reactive filtration. In this study, LCA demonstrates that reactive filtration has the potential as a negative emissions technology with −1.21 kg CO₂e/m³, where the negative contribution from the dosed biochar is −1.53 kg CO₂e/m³. In this biochar water treatment configuration, the system not only effectively removes pollutants from wastewater but also contributes to carbon sequestration and nutrient recovery for agriculture, making it a potentially valuable approach for sustainable water treatment. Full article

Sewage sludge, as a by-product of wastewater treatment, poses severe environmental challenges due to its high moisture, ash, and heavy metal content. Thermochemical conversion technologies, including pyrolysis and gasification, offer promising pathways for transforming sludge into valuable products such as bio-oil, biochar, and syngas. This paper systematically reviews recent advancements in pyrolysis and gasification, focusing on process optimization and catalyst development to enhance product quality and energy recovery. In pyrolysis, factors such as temperature, residence time, and heating rate significantly influence product yields and properties, while catalytic and co-pyrolysis approaches further improve product structure and reduce environmental risks. In gasification, parameters like the equivalence ratio, steam-to-sludge ratio, and catalyst application are key to enhancing syngas yield and quality, with biomass co-gasification offering additional benefits. Despite substantial progress, commercialization remains challenged by high operational costs, catalyst durability, and environmental impacts. Future research should emphasize improving sludge pretreatment, optimizing thermochemical processes, developing efficient and cost-effective catalysts, and addressing critical issues such as bio-oil quality, tar management, and syngas purification to promote the industrial application of these technologies. Full article

Arsenic contamination in water poses a significant global health risk, necessitating efficient and sustainable remediation strategies. Arsenic contamination affects groundwater in at least 106 countries, potentially exposing over 200 million people to elevated levels, primarily through contaminated drinking water. Among the most affected regions, Bangladesh remains a critical case study, where widespread reliance on shallow tubewells has resulted in one of the largest mass poisonings in history. Bio-based nanomaterials have emerged as promising solutions due to their eco-friendly nature, cost-effectiveness, and high adsorption capabilities. These nanomaterials offer a sustainable approach to arsenic remediation, utilizing materials like biochar, modified biopolymers, and bio-based aerogels, which can effectively adsorb arsenic and other pollutants. The use of environmentally friendly nanostructures provides a potential option for improving the efficiency and sustainability of arsenic remediation from groundwater. This review explores the mechanisms underlying arsenic remediation using such nanomaterials, including adsorption, filtration/membrane technology, photocatalysis, redox reactions, complexation, ion exchange, and coagulation–flocculation. Despite their potential, challenges such as scalability, stability, and regeneration hinder widespread application. We discuss recent advancements in material design, surface modifications, and hybrid systems that enhance performance. Finally, future perspectives are highlighted, including the integration of these bio-derived systems with smart sensing technologies, sustainable water-treatment frameworks, smart design, and life-cycle integration strategies, particularly for use in resource-constrained regions like Bangladesh and other globally impacted areas. Full article

Recently, research has increasingly focused on the introduction of non-precious metals and developing highly stable carriers to enhance catalyst performance. In this study, we successfully synthesized copper (Cu)-modified biochar catalysts utilizing a sequential approach involving enzymatic treatment, liquid impregnation, and activation processes, which effectively enhanced the dispersion and introduction efficiency of Cu onto the biochar, thereby reducing the requisite Cu loading while maintaining high catalytic activity. The experimental results showed that the toluene degradation of 10%Cu@BCL was three times higher than that of unmodified activated carbon (AC) at 290 °C. A more uniform distribution of Cu was obtained by the enzymatic and activation treatments, optimizing the catalyst’s structural properties and reducing the amount of Cu on the biochar. Moreover, the transformation between various oxidation states of Cu (from Cu⁰/Cu(I) to Cu(II)) facilitated the electron transfer during the degradation of toluene. To further understand the catalytic mechanisms, density functional theory (DFT) calculations were employed to elucidate the interactions between toluene molecules and the Cu-modified biochar surface. These findings reveal that the strategic modification of biochar as a carrier not only enhances the dispersion and stability of active metal species but contributes to improved catalytic performance, thereby enhancing its degradation efficiency for VOCs in high-temperature conditions. Full article