Search Results (44)

5-Hydroxymethylfurfural (HMF) is a versatile platform molecule with the potential to replace many fossil fuel derivatives. It can be obtained through the dehydration of carbohydrates. In this study, we present a simple and cost-effective microwave-assisted method for producing HMF. This method involves the use of readily available sucrose as a substrate and glucose-derived bifunctional hydrochars as carbocatalysts. These catalysts were produced via hydrothermal carbonisation using thiourea and urea as nitrogen and sulphur sources, respectively, to introduce Brønsted acidic and basic sites into the materials. Using a microwave reactor, we found that the S, N-doped hydrochars were active in sucrose dehydration in water. Catalytic results showed that HMF yield depended on the balance between acidic and basic sites as well as the types of S and N species present on the surfaces of these hydrochars. The best-performing catalyst achieved an encouraging HMF yield of 37%. The potential of N, S-co-doped biochar as a green solid catalyst for various biorefinery processes was demonstrated. A simple kinetic model was developed to elucidate the kinetics of the main reaction pathways of this cascade process, showing a very good fit with the experimental results. The calculated rate constants revealed that reactions with a 5% sucrose loading exhibited significantly higher fructose dehydration rates and produced fewer side products than reactions using a more diluted substrate. No isomerisation of glucose into fructose was observed in an air atmosphere. On the contrary, a limited rate of isomerisation of glucose into fructose was recorded in an oxygen atmosphere. Therefore, efforts should focus on achieving a high glucose-to-fructose isomerisation rate (an intermediate reaction step) to improve HMF selectivity by reducing humin formation. Full article

Sludge-derived biochar (SDB) synthesized by the pyrolysis of sludge is gaining enormous interest as a sustainable solution to wastewater treatment and sludge disposal. Despite the proliferation of general biochar reviews, a focused synthesis on SDB-specific advances, particularly covering the recent surge in multifunctional wastewater treatment applications (2020–2025), receives little emphasis. In particular, a critical analysis of recent trends, application challenges, and future research directions for SDB is still limited. Unlike broader biochar reviews, this mini-review highlights the comparative advantages and limitations of SDB, identifies emerging integration strategies (e.g., bio-electrochemical systems, catalytic membranes), and outlines future research priorities toward enhancing the durability and environmental safety of SDB applications. Specifically, this review summarized the advances from 2020 to 2025, focusing exclusively on functional modifications, and practical applications of SDB across diverse wastewater treatment technologies involved in adsorption, catalytic oxidation, membrane integration, electrochemical processes and bio-treatment systems. Quantitative comparisons of adsorption capacities (e.g., >99% Cd2+ removal, >150 mg/g tetracycline adsorption) and catalytic degradation efficiencies are provided to illustrate recent improvements. The potential of SDB in evaluating traditional and emerging contaminant degradation among the Fenton-like, persulfate, and peracetic acid activation systems was emphasized. Integration with membrane technologies reduces fouling, while electrochemical applications, including microbial fuel cells, yield higher power densities. To improve the functionality of SDB-based systems in targeting contamination removal, modification strategies, i.e., thermal activation, heteroatom doping (N, S, P), and metal loading, played crucial roles. Emerging trends highlight hybrid systems and persistent free radicals for non-radical pathways. Despite progress, critical challenges persist in scalability, long-term stability, lifecycle assessments, and scale-up implementation. The targeted synthesis of this review offers valuable insights to guide the development and practical deployment of SDB in sustainable wastewater management. Full article

The widespread industrial use of chromium has exacerbated water contamination issues globally. In this study, a nitrogen-doped wheat straw biochar loaded with nanoscale zero-valent iron composite (nZVI/N-KBC) was synthesized via a liquid-phase reduction method, and its adsorption properties for hexavalent chromium (Cr(VI)) in aqueous solutions were systematically investigated. The material was characterized using SEM, XRD, Raman spectroscopy, FTIR, and XPS. Experimental results demonstrated that under optimal conditions (pH 2, 0.05 g adsorbent dosage, and 50 mg/L initial Cr(VI) concentration), the adsorption capacity reached 41.29 mg/g. Isothermal adsorption analysis revealed that the process followed the Langmuir model, indicating monolayer adsorption with a maximum capacity of 100.9 mg/g. Kinetic studies show that the adsorption conforms to the pseudo-second-order kinetic model, and thermodynamic and XPS analyses jointly prove that chemical adsorption is dominant. Thermodynamic analyses confirmed the endothermic and entropy-driven nature of adsorption. Mechanistic studies via XPS and FTIR revealed a dual mechanism: (1) partial adsorption of Cr(VI) onto the nZVI/N-KBC surface, and (2) predominant reduction in Cr(VI) to Cr(III) mediated by Fe⁰ and Fe²⁺. This study highlights the synergistic role of nitrogen doping and nZVI loading in enhancing Cr(VI) removal, offering a promising approach for remediating chromium-contaminated water. Full article

Magnetic Fe and N-doped biochar (FeN-BC) was synthesized from waste bamboo through microwave pyrolysis and used as a catalyst for the degradation of tetracycline hydrochloride (TC) with peroxymonosulfate (PMS). The results showed that doping with Fe improved the recovery performance of biochar and the N-doping enhanced the activity of PMS. Simultaneously, it achieved a high degradation efficiency for TC (93%) under optimized conditions within 30 min. Electron paramagnetic resonance (EPR) and quenching experiments indicated that the main active radicals present in the experiment were SO₄^•− and •OH. Additionally, FeN-BC demonstrated good catalytic performance in the TC degradation process in a real water environment after five cycles. This work presents a practical strategy for preparing magnetic biochar to degrade organic pollutants from wastewater. Full article

Hydrogen production via water splitting is a crucial strategy for addressing the global energy crisis and promoting sustainable energy solutions. This review systematically examines water-splitting mechanisms, with a focus on photocatalytic and electrochemical methods. It provides in-depth discussions on charge transfer, reaction kinetics, and key processes such as the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). Various electrode synthesis techniques, including hydrothermal methods, chemical vapor deposition (CVD), pulsed laser deposition (PLD), and radio frequency sputtering (RF), are reviewed for their advantages and limitations. The role of carbon-based materials such as graphene, biochar, and graphitic carbon nitride (g-C₃N₄) in photocatalytic and photoelectrochemical (PEC) water splitting is also highlighted. Their exceptional conductivity, tunable band structures, and surface functionalities contribute to efficient charge separation and enhanced light absorption. Further, advancements in heterojunctions, doped systems, and hybrid composites are explored for their ability to improve photocatalytic and PEC performance by minimizing charge recombination, optimizing electronic structures, and increasing active sites for hydrogen and oxygen evolution reactions. Key challenges, including material stability, cost, scalability, and solar spectrum utilization, are critically analyzed, along with emerging strategies such as novel synthesis approaches and sustainable material development. By integrating water splitting mechanisms, electrode synthesis techniques, and advancements in carbon-based materials, this review provides a comprehensive perspective on sustainable hydrogen production, bridging previously isolated research domains. Full article

Advanced oxidation processes based on either peroxydisulfate (PDS) or peroxymonosulfate (PMS), collectively termed persulfate-based advanced oxidation processes (PS-AOPs), show potential in wastewater treatment applications. In this work, the nitrogen (N) and sulfur (S) co-doped biochar (NSBC) was prepared via a one-step pyrolysis of coffee grounds at 400 to 800 °C as a PMS activator for degrading paracetamol (PCT). The non-metallic NSBC demonstrated exceptional catalytic activity in activating PMS. In the NSBC-800/PMS system, 100% of PCT was completely degraded within 20 min, with a high reaction rate constant (k_obs) of 0.2412 min⁻¹. The system’s versatility was highlighted by its degradation potential across a wide pH range (3–11) and in the presence of various background ions and humic acids. The results of various experiments and characterization techniques showed that the system relied on an NSBC-800-mediated electron transfer as the main mechanism for PCT degradation. Additionally, there was a minor involvement of ¹O₂ in a non-radical degradation pathway. The graphitic N and thiophene-S (C-S-C) moieties introduced by N/S co-doping, as well as the carbonyl (C=O) groups of the biochar, were considered active sites promoting ¹O₂ generation. The total organic carbon (TOC) removal rate reached 37% in 120 min, while the assessment of the toxicity of the degradation products also affirmed the system’s environmental safety. This research provides a novel method for preparing environmentally friendly and cost-effective carbon-based catalysts for environmental remediation. Full article

Although the cultivation of food crops in farmland heavily contaminated by heavy metals is prohibited in China, vegetables can still be planted on a small-scale due to their short growth cycles and flexible sale models, posing a significant threat to local consumers. In this study, a pot culture experiment was conducted to investigate the feasibility of safe production through the in-situ stabilization of heavy metals in heavily contaminated soil. The remediation efficiency of wheat straw biochar and N-doped biochar, the growth of spinach, the heavy metal accumulation in spinach, and potential health risks were also explored. The results indicated that both biochar and N-doped biochar significantly affected the soil pH, cation exchange capacity, organic matter, available phosphorus, available potassium, alkaline nitrogen content, and spinach biomass, but the trends were variable. Additionally, the diethylenetriaminepentaacetic-extractable Pb, Cd, Cu, Zn, and Ni concentrations decreased 9.23%, 7.54%, 5.95, 7.44%, and 16.33% with biochar, and 10.46%, 12.91%, 21.98%, 12.62%, and 12.24% with N-doped biochar, respectively. Furthermore, N-doped biochar significantly reduced the accumulation of Pb, Cd, and Ni in spinach by 35.50%, 33.25%, and 30.31%, respectively. Health risk assessment revealed that the non-carcinogenic risk index for adults and children decreased from 17.0 and 54.8 to 16.3 and 52.5 with biochar and 11.8 and 38.2 with N-doped biochar, respectively, but remained significantly higher than the acceptable range (1.0). The carcinogenic risk assessment revealed that the risk posed by Cd in spinach exceeded the acceptable value (10⁻⁴) for both adults and children across all treatments. These results may imply that biochar and N-doped biochar cannot achieve the safe production of vegetables in soil heavily contaminated by heavy metals through in-situ stabilization. Full article

Mushroom production is increasing rapidly worldwide, raising public concern about the contamination effects of spent mushroom substrates (SMS). Preparation of Fe–N-doped biochar (Fe-N-BC) from SMS as a raw material for catalytic degradation of antibiotics in water may be an effective and sustainable solid waste treatment. However, there is limited information available. This study investigated the effect and potential mechanism of SMS-based Fe-N-BC prepared at 300, 600, and 900 °C to catalyze persulfate (PS) for tetracycline (TC) removal. The results indicated that the catalytic performance of Fe-N-BC was significantly enhanced with increasing pyrolysis temperature. Notably, Fe-N-BC prepared at 900 °C exhibited high TC removal efficiency, with 95% TC removal at 120 min. This might be closely related to the fact that the Fe-N-BC prepared at high temperatures had more Fe oxides and active sites. Adsorption and radical and non-radical pathways were the main mechanisms for TC removal by Fe-N-BC/PS systems, especially the contribution of SO₄·⁻. By identifying the degradation products, three possible pathways of TC degradation were proposed, and the toxicity of the degradation intermediates was evaluated. The results of the reusability analysis indicated that the Fe-N-BC prepared at 900 °C had good potential for practical application, and the TC removal rate still reached 76%, even after five cycles. These findings provide valuable reference information for solid waste resources’ sustainable utilization and the remediation of antibiotic-contaminated water. Full article

Single-layer slow-release materials have short lifespans due to their rapid initial release behavior. To address this problem, a double-coated persulfate slow-release material was developed in this study. The outer coating layer consists of polycaprolactone–silica sand, which is used to encapsulate an inner layer of polycaprolactone–silica sand and sodium persulfate. Static and dynamic release experiments were conducted to analyze the behavior and degradation capabilities of this material when activated by iron–nitrogen co-doped biochar (Fe@N-BC) for the removal of sulfamethoxazole (SMZ) and ciprofloxacin (CIP) in groundwater. The double-coated material maintains a stable release rate, achieving optimal performance with an outer layer thickness of 0.25 cm and a silica sand to polycaprolactone (PCL) mass ratio between 2 and 5. Optimal degradation rates for SMZ and CIP were observed at a pH of 3. Specifically, 1 mg/L of SMZ was fully degraded within 12 h, while the complete removal of 1 mg/L of CIP occurred within just 2 h. The presence of humic acid and higher initial pollutant concentrations reduced the degradation rates. Among the tested anions, HCO₃⁻ had the most significant inhibitory impact, while Cl⁻ had the least significant impact on degradation performance. Column experiments demonstrated a consistent release of persulfate over a period of 60 days at a flow rate of 0.5 mL/min. Increased flow rates resulted in a shorter lifespan for this slow-release material. The minimum outflows of SMZ and CIP were obtained with a quartz sand mesh size of 40–60 and a flow rate of 0.5 mL/min. These results offer a theoretical basis for the prolonged and stable release of persulfate, as well as the efficient removal of SMZ and CIP from groundwater. Full article

The development of sustainable and high-performance oxygen reduction reaction (ORR) electrocatalysts is fundamental to fuel cell implementation. Non-precious transition metal oxides present interesting electrocatalytic behavior, and their incorporation into N-doped carbon supports leads to excellent ORR performance. Herein, we prepared a shrimp shell-derived biochar (CC), which was doped with nitrogen via a ball milling approach (N-CC), and then used as support for Co₃O₄ nanoparticles growth (N-CC@Co₃O₄). Co₃O₄ loading was optimized using three different amounts of cobalt precursor: 1.56, 2.33 and 3.11 mmol in N-CC@Co₃O₄_1, N-CC@Co₃O₄_2 and N-CC@Co₃O₄_3, respectively. Interestingly, all prepared electrocatalysts, including the initial biochar CC, presented electrocatalytic activity towards ORR. Both N-doping and the introduction of Co₃O₄ NPs had a significant positive effect on ORR performance. Meanwhile, the three composites showed distinct ORR behavior, demonstrating that it is possible to tune their electrocatalytic performance by changing the Co₃O₄ loading. Overall, N-CC@Co₃O₄_2 achieved the most promising ORR results, displaying an E_onset of 0.84 V vs. RHE, j_L of −3.45 mA cm⁻² and excellent selectivity for the 4-electron reduction (n = 3.50), besides good long-term stability. These results were explained by a combination of high content of pyridinic-N and graphitic-N, high ratio of pyridinic-N/graphitic-N, and optimized Co₃O₄ loading interacting synergistically with the porous N-CC support. Full article

In this study, Fe, N co-doped biochar (Fe@N co-doped BC) was synthesized by the carbonization–pyrolysis method and used as a carbocatalyst to activate peroxymonosulfate (PMS) for sulfamethoxazole (SMX) removal. In the Fe@N co-doped BC/PMS system, the degradation efficiency of SMX (10.0 mg·L⁻¹) was 90.2% within 40 min under optimal conditions. Radical quenching experiments and electron spin resonance (ESR) analysis suggested that sulfate radicals (SO₄^•−), hydroxyl radicals (^•OH), and singlet oxygen (¹O₂) participated in the degradation process. After the reaction, the proportion of pyrrolic N decreased from 57.9% to 27.1%. Pyrrolic N served as an active site to break the inert carbon network structure and promote the generation of reactive oxygen species (ROS). In addition, pyrrolic N showed a stronger interaction with PMS and significantly reduced the activation energy required for the reaction (∆G = 23.54 kcal/mol). The utilization potentiality of Fe@N co-doped BC was systematically evaluated in terms of its reusability and selectivity to organics. Finally, the intermediates of SMX were also detected. Full article

Using rapeseed straw as a raw material and potassium bicarbonate (KHCO₃) and urea (CO(NH₂)₂) as modification reagents, the pyrolysis raw materials were mixed in a certain proportion, and the unmodified biochar GBC800, KHCO₃-modified biochar KGBC800, and (KHCO₃)/(CO(NH₂)₂) co-modified biochar N-KGBC800 were, respectively, prepared using the one-pot method at 800 °C. The physicochemical properties, such as surface morphology, pore characteristics, functional group distribution, and elemental composition of the three biochars, were characterized, and the adsorption performance and mechanism of the typical antibiotic tetracycline (TC) in water were studied. The results showed that the surface of GBC800 was smooth and dense, with no obvious pore structure, and both the specific surface area and total pore volume were small; the surface of KGBC800 showed an obvious coral-like three-dimensional carbon skeleton, the number of micropores and the specific surface area were significantly improved, and the degree of carbonization and aromatization was enhanced; N-KGBC800 had a coral-like three-dimensional carbon skeleton similar to KGBC800, and there were also many clustered carbon groups. The carbon layer changed significantly with interlayer gaps, presenting a multi-level porous structure. After N doping, the content of N increased, and new nitrogen-containing functional groups were formed. When the initial TC concentration was 100 mg/L, pH ≈ 3.4, the temperature was 25 °C, and the dosage of the three biochars was 0.15 g/L, the adsorption equilibrium was reached before 720 min. The adsorption capacities of GBC800, KGBC800, and N-KGBC800 for TC were 16.97 mg/g, 294.86 mg/g, and 604.71 mg/g, respectively. Fitting the kinetic model to the experimental data, the adsorption of TC by the three biochars was more in line with the pseudo-second-order adsorption kinetic model, and the adsorption isotherm was more in line with the Langmuir model. This adsorption process was a spontaneous endothermic reaction, mainly chemical adsorption, specifically involving multiple adsorption mechanisms such as pore filling, electrostatic attraction, hydrogen bonds, n−π interaction, Lewis acid–base interaction, π−π stacking, or cation −π interaction between the aromatic ring structure of the carbon itself and TC. A biochar-adsorption column was built to investigate the dynamic adsorption process of tetracycline using the three biochars against the background of laboratory pure water and salt water. The adsorption results show that the Thomas model and the Yoon–Nelson model both provide better predictions for dynamic adsorption processes. The modified biochars KGBC800 and N-KGBC800 can be used as preferred materials for the efficient adsorption of TC in water. Full article

The doping of porous carbon materials with nitrogen is an effective approach to enhance the electrochemical performance of electrode materials. In this study, nitrogen-doped porous carbon derived from peanut shells was prepared as an electrode for supercapacitors. Melamine, urea, urea phosphate, and ammonium dihydrogen phosphate were employed as different nitrogen dopants. The optimized electrode material PA-1-1 prepared by peanut shells, with ammonium dihydrogen phosphate as a nitrogen dopant, exhibited a N content of 3.11% and a specific surface area of 602.7 m²/g. In 6 M KOH, the PA-1-1 electrode delivered a high specific capacitance of 208.3 F/g at a current density of 1 A/g. Furthermore, the PA-1-1 electrode demonstrated an excellent rate performance with a specific capacitance of 170.0 F/g (retention rate of 81.6%) maintained at 20 A/g. It delivered a capacitance of PA-1-1 with a specific capacitance retention of 98.8% at 20 A/g after 5000 cycles, indicating excellent cycling stability. The PA-1-1//PA-1-1 symmetric supercapacitor exhibited an energy density of 17.7 Wh/kg at a power density of 2467.0 W/kg. This work not only presents attractive N-doped porous carbon materials for supercapacitors but also offers a novel insight into the rational design of biochar carbon derived from waste peelings. Full article

Nutrient pollution poses a significant global environmental threat, and addressing this issue remains an ongoing challenge. Biochar has been identified as a potential adsorbent for environmental remediation. However, raw biochar has a low nitrate adsorption capacity; thus, biochar modification is necessary for targeted environmental applications. This work explored and compared the performance of Fe-doped, N-doped, and N-Fe-co-doped biochars from Douglas fir toward nitrate removal from an aqueous solution. A central composite experimental design was used to optimize processing variables, maximizing the surface area and nitrate adsorption capacity. Proximate analysis, elemental composition, gas physisorption, XPS, SEM, TEM, FTIR, and XRD were used to characterize the biochar’s properties. Pyrolysis under NH₃ gas generated more pores in biochar than conventional pyrolysis. Doping biochar with N and Fe improved nitrate adsorption capacity from aqueous solutions. The maximum nitrate adsorption capacity of Fe-N-doped biochar produced at 800 °C was 20.67 mg g⁻¹ in sorption tests at pH 3.0. The formation of N-containing functional groups and Fe oxides on the biochar surface enhanced the nitrate removal efficiency of N-Fe biochar. The results indicate that biochar’s adsorption capacity for NO₃⁻ is largely affected by the solution’s pH and biochar’s surface chemistry. Electrostatic attraction is the primary mechanism for nitrate adsorption. Full article