Adsorption Capacity Of Biochar Research Articles

Efficiency of dye adsorption of modified biochar: A comparison between chemical modification and ball milling assisted treatment

Ball milling technology was employed to increase the adsorption capacity of biochar with respect to methylene blue as a model pollutant. Comparative studies on the adsorption ability were conducted on ball-milled biochar and biochar chemically modified by oxidation and alkaline treatment, showing that ball milling produces higher performances since increases available active sites. The particle size reduction, with the consequence of an increase in the surface area was hypothesized to be responsible for the high removal efficiency. The adsorption kinetics follows a pseudo-second-order model, implying that the process is affected by chemisorption. Moreover, the Langmuir model proved that the maximum monolayer adsorption capacity increased to 185.18 mg/g. Design of experiments allowed for evaluating the pH and initial concentration values, which maximized the removal efficiency. The milled biochar was also regenerated and reused over six times, resulting in a drop of only 1 %.

Advancements in application of modified biochar as a green and low-cost adsorbent for wastewater remediation from organic dyes

Synthetic organic dyes, which are resistant to biodegradation, pose a notable health risk, potentially leading to cancer and respiratory infections. Researchers have addressed this concern by exploring physicochemical methods to remove organic dyes from wastewater. A particularly promising solution involves modified biochar adsorbents, which demonstrate high efficiency in organic dye removal. Biochar, a charcoal-like material derived from biomass pyrolysis, offers advantages such as low cost, eco-friendliness, high efficiency and reusability. Beyond its role in sustainable soil remediation, biochar proves effective in removing organic dyes from wastewater after undergoing physical or chemical modification. Acid–base activation or metal–heteroatom impregnation enhances biochar's adsorption capacity. This comprehensive review examines the attributes of biochar, common methods for production and modification, and the impacts of raw materials, pyrolysis temperature, heating rate and residence time. It further elucidates the biochar adsorption mechanism in the removal of organic dyes, assessing factors influencing efficiency, including biochar feedstock, solution pH, adsorption temperature, particle size, initial dye concentration, biochar dosage and reaction time. It explores challenges, opportunities, reusability and regeneration methods of biochar in treating organic dye wastewater. It also discusses recent advances in organic dye removal using adsorption-based biochar. The review ultimately advocates for enhancing biochar's adsorption performance through post-modification.

Investigating the potential of mineral precipitation in co-pyrolysis biochar: Development of a novel Cd (II) adsorption material utilizing dual solid waste

Ionic cadmium (Cd (II)) in water is a significant threat to ecosystems, the environment, and human health. Research is currently focused on developing efficient adsorption materials to combat Cd (II) pollution in water. One promising solution involves co-pyrolyzing solid residue from anaerobic digestion of food waste with oil-based drill cuttings pyrolysis residue to create a biochar with high organic matter content. This biochar has a lower heavy metal content and leaching toxicity compared to China's national standards, making it both safe and resourceful. It exhibits a high adsorption capacity for Cd (II) in water, reaching up to 47.80 ± 0.37 mg/g. Raising the pyrolysis temperature above 600 °C and increasing the amount of pyrolysis residue beyond 30 % enhances the biochar's adsorption capacity. The adsorption process is primarily driven by mineral precipitation, offering a promising approach for dual waste resource management and reducing heavy metal pollution.

Biochar design for antibiotics adsorption via a hybrid machine-learning-based optimization framework

Biochar is widely applied as an adsorbent for removing contaminants. Herein, two machine learning (ML) models for biochar preparation and adsorption application were trained based on the eXtreme Gradient Boosting algorithm. Then, the two models were combined by developing a hybrid ML-based optimization framework via Particle Swarm Optimization to design biochar for application requirements. The test determination coefficient for predicting specific surface area (SSA), total volume, and adsorption capacity of biochar were 0.85, 0.88, and 0.97 with root mean square error of 63.10 m2/g, 0.07 cm3/g, and 65.72 μmol/g, respectively. Moreover, SSA was the foremost and positive property of biochar for its adsorption capacity; and pyrolysis temperature and feedstock ash content were the two most important factors affecting SSA, among which the former was positively related and the latter had a negative impact. Optimization results indicated that pine wood pyrolyzed at 500–700 °C could prepare a biochar with higher antibiotic adsorption capacity. This work presents an intelligent strategy to design biochar for adsorbing target pollutants.

Treatment of aqueous per- and poly-fluoroalkyl substances: A review of biochar adsorbent preparation methods

Per- and poly-fluoroalkyl substances (PFAS) are synthetic chemicals widely used in everyday products, causing elevated concentrations in drinking water and posing a global challenge. While adsorption methods are commonly employed for PFAS removal, the substantial cost and environmental footprint of commercial adsorbents highlight the need for more cost-effective alternatives. Additionally, existing adsorbents exhibit limited effectiveness, particularly against diverse PFAS types, such as short-chain PFAS, necessitating modifications to enhance adsorption capacity. Biochar can be considered a cost-effective and eco-friendly alternative to conventional adsorbents. With abundant feedstocks and favorable physicochemical properties, biochar shows significant potential to be applied as an adsorbent for removing contaminants from water. Despite its effectiveness in adsorbing different inorganic and organic contaminants from water environments, some factors restrict its effective application for PFAS adsorption. These factors are related to the biochar properties, and characteristics of PFAS, as well as water chemistry. Therefore, some modifications have been introduced to overcome these limitations and improve biochar's adsorption capacity. This review explores the preparation conditions, including the pyrolysis process, activation, and modification techniques applied to biochar to enhance its adsorption capacity for different types of PFAS. It addresses critical questions about the adsorption performance of biochar and its composites, mechanisms governing PFAS adsorption, challenges, and future perspectives in this field. The surge in research on biochar for PFAS adsorption indicates a growing interest, making this timely review a valuable resource for future research and an in-depth exploration of biochar's potential in PFAS remediation.

Effect of biochar structure on the selective adsorption of heavy components in bio‐oil

AbstractIn this study, biochars with different structures were prepared through HNO3 oxidation and secondary pyrolysis to study the relationship between the structure of biochar and its selectivity for the adsorption of light and heavy aromatics in bio‐oil. The results showed that the adsorption rates of biochar with different structures ranged from 2.90 to 4.00 g bio‐oil per g biochar. The influence of pore structure was dominant, followed by the influence of O‐containing functional groups and the degree of graphitization. The higher the adsorption capacity of biochar for bio‐oil, the smaller the concentrations of the light aromatic model compounds in the absorbed bio‐oil (ABO). Among the five light aromatics, biochar has the best adsorption selectivity for dihydroxybiphenyl and the worst for eugenol and propyl phenol. This is attributed to the diphenyl ring structure of dihydroxybiphenyl, which makes it more susceptible to adsorption, and other light model compounds only have one benzene ring. In summary, biochar demonstrates better adsorption selectivity for heavy aromatics than light aromatics. The more developed the pore structure is, the more enriched O‐containing functional groups are, and the higher the graphitization degree of biochar is, the better the selective adsorption of aromatic compounds in bio‐oil.

Insights into microplastics (MPs) removal using aquatic plant-derived biochar from Taihu Lake at varying carbonization temperatures

Microplastics (MPs), recognized as significant emerging contaminants, are prevalent in both terrestrial and aquatic ecosystems. This study investigates the potential of biochar derived from Polygonum amphibium L. (PAL) sourced from Taihu Lake and processed through a low-temperature carbonization method, for in the removal of MPs. This approach addresses the escalating presence of MPs in aqueous environment, especially during the COVID-19 pandemic, simultaneously tackles the issue of waste biomass contributing to eutrophication. The study focused on the impact of carbonization temperatures (450℃-550℃) on physicochemical properties of biochar. Additionally, the effect of contact time, initial concentration of MPs, and environmental factors at various carbonization temperatures were also examined. The results reveal that the biochar yield and adsorption performance of biochar are significantly influenced by carbonization temperature. The adsorption capacity of biochar for MPs removal increases with the carbonization temperature up to 500 ℃, attributed to enhanced diffusion, surface adsorption, interactions, and cation-π electron interactions between the biochar and MPs. However, at a pyrolysis temperature of 550 ℃, the increase in adsorption capacity of biochar-550 is marginal due to increased competitive binging and destabilization of biochar under basic conditions. Overall, the optimum carbonization temperature is identified as 500 ℃, yielding a char rate is 32.23% and an adsorption capacity for MPs of 80.3 mg/g, thereby offering a promising solution for MP removal and water eutrophication management.

Effective adsorption of norfloxacin from water on magnetic biochar composite derived from cellulase hydrolysis apple branch: Synthesis optimization, performance assessment and mechanism insight

Based on the optimization of feedstock and temperature condition, we synthesized a novel biochar composite (CHMAB) by pyrolyzing apple branch after cellulase hydrolysis and magnetization as well as coating them with humic acid (HA). Compared with the simultaneously prepared magnetic biochar (MAB) and HA-coated magnetic biochar (HMAB), batch adsorption test results showed that CHMAB had the best norfloxacin (NOR) removal performance in a wide pH range (2−12). The endothermic and spontaneous adsorption behavior of NOR on CHMAB could be better suited to the pseudo-second-order model and Langmuir model with maximum absorption capacity (81.08 mg g−1) at 35℃. Pore filling, π-π EDA interactions, hydrogen bonding, surface complexation, electrostatic interactions and hydrophobic interactions might all be implicated in the NOR removal process. Additionally, the regenerated CHMAB still maintained 99.23% removal efficiency for 0.1 mol L−1 NOR and performed well after seven cycles. These findings highlighted the possibility of enhancing the adsorption capacity of biochar for antibiotics by modification through cellulase hydrolysis of precursor and HA coating procedure. It is noteworthy that the use of low-cost agricultural and forestry wastes to produce adsorbents for emerging contaminants such as antibiotics could have greater potential for future practical applications under the ongoing dual carbon policy.

Lignin-impregnated biochar assisted with microwave irradiation for CO2 capture: adsorption performance and mechanism

Bamboo biochar was modified by lignin impregnation and microwave irradiation to enhance its performance for CO2 capture. The pore structure of lignin-impregnated biochar was significantly affected by the impregnation ratio. The maximum specific surface area of 377.32 m2 g−1 and micropore volume of 0.163 cm3 g−1 were observed on the biochar with an impregnation ratio of 1:20 (mass ratio of lignin to biochar). Lignin impregnation increased the CO2 adsorption capacity of biochar up to 134.46 mg g−1. Correlation analysis confirmed the crucial role of biochar’s pore structure in adsorption. The Avrami model fitted the CO2 capture curves well. The calculation of adsorption activation energy suggested that the adsorption process was dominated by physical mechanism assisted with partial chemical mechanism. Meanwhile, Langmuir isotherm analysis indicated that lignin impregnation transformed the larger pores of biochar into more uniform micropores, thereby making the adsorption process closer to monolayer adsorption. Both the high reusability (89.79–99.06%) after 10 successive cycles and the excellent CO2 selectivity in competitive adsorption confirmed that lignin-impregnated biochar is an outstanding adsorbent for CO2 capture.Graphical

Respective evolution of soil and biochar on competitive adsorption mechanisms for Cd(II), Ni(II), and Cu(II) after 2-year natural ageing

To reveal the respective evolution of soil and biochar on competitive heavy metal adsorption mechanisms after natural ageing, three soils and two biochars were tested in this study. The soil-biochar interlayer samples were buried in the field for 0.5, 1, and 2 years, for which competitive adsorption characteristics and mechanisms of soils and biochars in four systems (Cd, Cd+Ni, Cd+Cu, and Cd+Ni+Cu) were investigated. Results showed that physicochemical properties, adsorption capacity and mechanisms of soils and biochars all changed the most in the first 0.5 years. The properties and adsorption capacity of biochars gradually weakened with the ageing time, meanwhile, those of soils gradually enhanced. After co-ageing with acidic soil for 0.5 years, the Cd(II) adsorption capacity of modified biochar decreased by 86.59% in the ternary system; meanwhile, that of acidic soil increased by 65.52%. The contributions of mineral mechanisms decreased significantly, while non-mineral mechanisms were slightly affected by ageing. This study highlighted that when using biochar to remediate heavy metal-contaminated soils, biochar should be applied at least half a year in advance before planting crops so that biochar can fully contact and react with the soil.

Competitive Adsorption of Cd(II) and Zn(II) on Biochar, Loess, and Biochar-loess Mixture

Combined heavy metal contamination in soil is a common phenomenon. Biochar amendment into the soil is considered to be an alternative for immobilization remediation of soil contaminated with heavy metals due to its adsorption and alkalization. However, much attention has been paid to the adsorption and immobilization of single heavy metals by biochar. In this paper, the competitive adsorption of Cd(II) and Zn(II) on biochar derived from cotton straw and pig manure at 500℃ (BCS500 and BPM500), loess and biochar-loess mixtures were investigated using the batch equilibrium method. The results showed that the adsorption capacities of biochars, loess, and biochar-loess mixtures to Cd(II) and Zn(II) in the mixed Cd-Zn systems increased with the increase of initial metal concentrations of Cd(II) and Zn(II). The adsorptive capacities of BCS500 and BPM500 to Cd(II) in mixed Cd-Zn system were 33% and 35% less than those in the single Cd(II)systems, while the adsorptive capacities to Zn(II) were 62% and 56% less than those in the single Zn(II) systems. The adsorptive capacities of loess to Cd(II) and Zn(II) in mixed Cd-Zn systems were 29% and 55% less than those in the single metal systems. The adsorptive capacities of loess-BCS500 (LBCS) and loess-BPM500 (LBPM) to Cd(II) in mixed Cd-Zn system were 40% and 38% less than those in the single Cd(II) systems, while the adsorptive capacities to Zn(II) were 63% and 60% less than those in the single Zn(II)systems. Moreover, the competitive adsorptive capacity of Cd(II) is greater than that of Zn(II). It can be seen that when heavy metal pollution with similar nature of multiple elements exists in soil, the amount of adsorbent should be increased to resist the possible weakened adsorption caused by competitive adsorption in order to guarantee an effective absorption treatment.

New insights into biochar ammoniacal nitrogen adsorption and its correlation to aerobic degradation ammonia emissions

One of the technical barriers to the wider use of biochar in the composting practices is the lack of accurate quantification linking biochar properties to application outcomes. To address this issue, this paper investigates the use of ammonia nitrogen adsorption capacity by biochar as a predictor of ammonia emission during composting in the presence of biochar. With this in mind, this work investigated the use of ammonia nitrogen adsorption capacity of biochar when mixed with solid digestate, and the reduction in ammonia emissions resulting from the addition of biochar during aerobic degradation of solid digestate. A biochar synthesized at 900 °C, another synthesized at 450 °C, and two derivatives of the latter biochar, one chemically modified with nitric acid and the other with potassium hydroxide, were tested. This study concluded that the chemical characteristics of the biochar, including pH and oxygen/carbon atomic ratio, had a greater influence on the adsorption of ammonia nitrogen than physical attributes such as specific surface area. In this regard, nitric acid modification had superior performance compared to hydroxide potassium modification to increase biochar chemical attributes and reduce ammonia emissions when applied to aerobic degradation. Finally, a significant linear correlation (p-value < 0.05, r2 = 0.79) was found between biochar ammonia nitrogen adsorption capacity and ammonia emissions along composting, showing the potential of this variable as a predictive parameter. This study provides insights for future explorations aiming to develop predictive tests for biochar performance.

Ball-Milled Biochar from Waste Bamboo Chopsticks: A Potential Adsorbent for Methylene Blue Removal

Waste bamboo chopsticks encounter limited recycling. Several treatment procedures necessitate sophisticated technologies and intricate processes that need more practicality for local-scale production, leading to substantial challenges in effectively repurposing waste from disposable bamboo chopsticks. In this research, waste bamboo chopsticks were used as raw materials for the production of ball-milled biochar (BM-WBCB). FTIR, SEM, and BET were among the numerous analytical methods used to describe the BM-WBCB. The outcomes showed that the surface was made up of hollow, porous structures. In addition, the pHpzc value of the biochar was 8.7, and it had a BET-specific surface area (273.11 m2 g-1). The study also investigated ball-milled biochar's adsorption capacity and efficiency in removing MB from aqueous solutions. Batch adsorption experiments were conducted under various experimental conditions, such as initial dye concentration, contact time, pH, and adsorbent dose, to evaluate the adsorption kinetics, equilibrium, and thermodynamics of the adsorption process. The results showed the optimal adsorption conditions, such as pH solution, MB concentration, dose of BM-WBCB, and contact time at 10, 30 mg L-1, 0.3 mg, and 60 min, respectively. With a maximal adsorption capacity of 4.2 mg g-1, monolayer adsorption was shown by the fit of the adsorption isotherm data to the Langmuir isotherm model. It was demonstrated that the kinetics of biochar adsorption may be accurately modeled using the linear pseudo-second-order kinetic model.

Nitrogen Removal from Landfill Leachate Using Biochar Derived from Wheat Straw.

Landfill leachate (LLCH) disposal poses challenges due to high pollutant concentrations. This study investigates the use of biochar (BC) derived from wheat straw for nitrogen content reduction. Laboratory experiments evaluated BC's adsorption capacity (qm) for nitrogen removal from ammonium chloride solution (NH4Cl) and LLCH, along with testing isotherm models. The results demonstrated that BC was more efficient (95.08%) than commercial activated carbon AC (93.11%), the blank, in adsorbing nitrogen from NH4Cl. This superior performance of BC may be attributed to its higher carbon content (57.74%) observed through elemental analysis. Lower results for BC/LLCH may be due to LLCH's complex chemical matrix. The Langmuir isotherm model best described BC/NH4Cl adsorption (qm = 0.5738 mg/g). The AC/NH4Cl data also fitted into the Langmuir (R2 ˃ 0.9) with a qm of 0.9469 mg/g, and 26.667 mg/g (R2 ˂ 0.9) was obtained for BC/LLCH; the BC/LLCH also gave higher qm (R2 ˃ 0.9) using the Jovanovich model (which also follows Langmuir's assumptions). The mean energy of the adsorption values estimated for the AC/NH4Cl, BC/NH4Cl, and BC/LLCH processes were 353.55, 353.55, and 223.61 kJ/mol, respectively, suggesting that they are all chemisorption processes and ion exchange influenced their adsorption processes. The Freundlich constant (1/n) value suggests average adsorption for BC/LLCH. The BC/LLCH data followed the Harkins-Jura model (R2: 0.9992), suggesting multilayered adsorption (or mesopore filling). In conclusion, biochar derived from wheat straw shows promising potential for landfill leachate remediation, offering efficient nitrogen removal capabilities and demonstrating compatibility with various adsorption models. This research also lays the groundwork for further exploration of other biochar-based materials in addressing environmental challenges associated with landfill leachate contamination.

Effects of different aging methods on the ability of biochar to adsorb heavy metal cadmium and its physical and chemical properties.

The aging process can affect the physical and chemical properties as well as adsorption capacity of biochar. This study focuses on the heavy metal cadmium (Cd) as the research object, and artificially ages biochar prepared from rice straw and corn straw through accelerated freeze-thaw cycles, alternating dry wet cycles, and ultraviolet light treatment, in order to evaluate the effects of different aging conditions on the physical and chemical properties of the two different types of biochar and on their adsorption capacities for Cd. After aging, the pH of rice and corn biochar decreased to varying degrees, respectively. The surface structure was ruptured, the average pore diameter was decreased, and the specific surface area was increased by 27.3%, 21.9%, and 9.8% (rice) and 95.4%, 27.7%, and 13.4% (corn). Ultraviolet light aging has the most significant impact on the elemental content of biochar, and the C content was decreased by 12.4% (rice) and 9.3% (corn). The O content was increased by 11.2% (rice) and 44.1% (corn), and the numbers of O/C, H/C, (O + N)/C, and oxygen-containing functional groups were increased. These results demonstrate that the aging process reduces the degree of aromatization of biochar, while enhancing its polarity and Cd adsorption capacity. Rice straw biochar (RSB) has a greater ability to adsorb Cd than corn straw biochar (CSB). In addition, ultraviolet light aging is particularly effective in increasing heavy metal adsorption.

Role of biochar pyrolysis temperature on intracellular and extracellular biodegradation of biochar-adsorbed organic compounds

Immobilizing organic pollutants by adsorption of biochar in farmland soil is a cost-effective remediation method for contaminated soil. As the adsorption capacity of biochar is limited, biodegradation of biochar-adsorbed organic pollutants was a potential way to regenerate biochars and maintain the adsorption performance of biochars to lower the cost. It could be affected by the biochar pyrolysis temperature, but was not evaluated yet. In this study, biodegradation of adsorbed phenanthrene on a series of biochars with pyrolysis temperatures from 150 to 700 °C by Sphingobium yanoikuyae B1 was investigated using batch experiments of biodegradation kinetics at 30 °C, to explore the role of biochar pyrolysis temperature on biodegradation of biochar-adsorbed organic compounds. It was observed that 37.5–47.9% of adsorbed phenanthrene on moderate temperature-pyrolyzed biochars produced at 400 and 500 °C were biodegraded, less than that on high temperature-pyrolyzed biochars produced at ≥600 °C (48.8–60.8%) and low temperature-pyrolyzed biochars produced at ≤300 °C (63.4–92.5%). Phenanthrene adsorbed largely on the low temperature-pyrolyzed biochars by partition mechanism and thus is easily desorbed to water for a dominated intracellular biodegradation. On the high temperature-pyrolyzed biochars, phenanthrene is adsorbed largely by pore-filling mechanism and thus less desorbed to water for intracellular biodegradation. However, high temperature-pyrolyzed biochars can promote microbes to produce siderophore, H2O2 and thus release extracellular •OH for a dominated degradation of adsorbed phenanthrene by Fenton-like reaction. With the increase of biochar pyrolysis temperature, desorption and consequently the intracellular biodegradation of adsorbed phenanthrene on biochars decreased, while the secretion of siderophore and H2O2 by microbes on biochars increased to produce more extracellular •OH for degradation by Fenton-like reaction. The results could provide deep insights into the role of biochar pyrolysis temperature on biodegradation of biochar-adsorbed organic compounds, and optimize the selection of biochar with higher adsorption performance and easier regeneration for soil remediation.

Effect of Ca Modified Biochar on the Chemical Speciation of Soil Phosphorus and Its Stabilization Mechanism

To control of phosphorus release from soil after farmland inundation around the lake and reservoir， calcium modified biochar （Ca-BC） was prepared using the coprecipitation method. Through X-ray photoelectron spectroscopy （XPS）， X-ray polycrystalline powder diffraction （XRD）， adsorption experiments， and simulated culture experiments， the effects of Ca-based biochar on the fraction of soil phosphorus （P） and its stabilization mechanism were studied. The results showed that the adsorption process of Ca-based modified biochar conformed to Langmuir （R2 = 0.940） and the first-order adsorption kinetic model （R2 = 0.961）， indicating that the P adsorption was a single-layer adsorption dominated by chemical action， and the maximum adsorption capacity was 267.93 mg·g-1. The simulated culture experiment indicated that when the modified biochar was 1%， the exchangeable fraction of phosphorus in the soil decreased from 7.42% to 4.59%. The XRD results demonstrated that Ca3（PO4）2 and hydroxyapatite absorption peaks appeared after adsorbed phosphorus on biochar， which proved that phosphate formed a relatively stable crystal precipitation. As shown in the XPS spectrum analysis， the carbonyl functional groups participated in the phosphorus fixation process， which improved the adsorption capacity of biochar for phosphorus. In general， when the concentration of Ca-based modified biochar was greater than 1%， it had a good fixation capacity for phosphorus release and had potential application value for controlling phosphorus release in soil.

Standardization and micromechanistic study of tetracycline adsorption by biochar

Modification serves as an excellent approach to enhancing the adsorption performance of biochar for tetracycline. Selective modification further allows the attainment of biochar materials that are not only more efficient but also cost-effective. However, the key structural factors influencing the adsorption of tetracycline by biochar remain unclear at present, hindering the effective guidance for modification strategies. This study established the relationship between carbonization degree and adsorption capacity, constructed a standardized microscopic model for biochar adsorption of tetracycline, and explored potential reaction mechanisms. The results indicated that with increases in the degree of carbonization, the tetracycline adsorption capacity of biochar increased from 16.08 mg L−1 to 98.35 mg L−1. The adsorption energy exhibited a strong correlation with the aromatic condensation of biochar at p ≤ 0.01, with a linear relationship (r2 ≥ 0.94). For low carbonization degrees, the adsorption of tetracycline by biochar was primarily driven by chemical bonds (69.21%) and complemented with electrostatic interactions, weak van der Waals forces or π-π interactions. For high carbonization degrees, the synergistic effects of hydrogen bonding, van der Waals forces, and π-π interactions determined the adsorption of tetracycline on biochar (91.1%). Additionally, larger carbon clusters resulted in stronger and more stable adsorption interactions. Furthermore, carboxyl-functionalized highly carbonized biochar displayed the highest reaction energy of − 1.8370 eV for adsorption of tetracycline through electrostatic interactions. This study suggests that a high degree of aromatic condensation in the carbon structure of biochar is crucial for the efficient adsorption of tetracycline.Graphical

Preparation of biochar adsorption material from walnut shell by supercritical CO2 pretreatment

In order to treat dyes in the wastewater of the printing industry and to reutilize walnut shell (WS) waste generate economic benefits, supercritical carbon dioxide (SC-CO2) pretreatment technology was developed to prepare porous biochar as a precursor for adsorption material. Orthogonal experiments were conducted at the temperatures of 200, 300, and 400 ℃ with durations of 20, 40, and 60 min, and a control group was set up using N2 pretreatment. Then, KOH activation was employed to prepare biochar adsorption material. The biochars were analyzed and characterized using TGA, BET, SEM, FT-IR, and XRD, and the liquid and gas phase products of the pretreatment process were analyzed semi-quantitatively and quantitatively using GC–MS and gas chromatography. Methylene blue (MB) dye was selected as an indicator to measure the adsorption capacity of biochar, and adsorption kinetics were analyzed based on the data. The results indicate that pretreatment with SC-CO2 effectively enhanced the performance and yield of the activated carbon. The highest specific surface area increased by 18%, and the maximum adsorption of MB increased by 23% compared to the N2 control group. The yield increased by 8–262% and the specific surface area increased by 50–192% compared to the direct activation of walnut shell (WS). During the pretreatment processes for the preparation of biochar adsorption material with the best specific surface area, phenol-enriched bio-oil was produced as a by-product which has economic value.Graphical

Conversion of biobased substances into biochar to enhances nutrient adsorption and retention capacity.

Reducing the environmental issues brought on by nutrients especially nitrogen pollution and loss is important. Owing to its unique composition and physico-chemical characteristics, biomass-derived biochar exhibits varying degrees of adsorption and interception for all types of soil nutrients. Thus, a novel way to improve nutrient absorption in the soil is to include biomass derived biochar into it. Various biomass-derived biochar from locally available biobased substances was synthesized through low-cost portable charring kiln. It has been quantified the influence of four biobased substances and three pyrolysis temperature on different morphomineralogical characteristics of biochar for utilizing as low-cost sorbent to manage nutrient adsorption and retention capacity. The morphomineralogical characteristics were principally manipulated by feedstocks rather than pyrolysis temperature. Higher porosity and surface area of biomass-derived biochar illustrated its soil structural modification and nutrient retention capacity along with their utilization for adsorbents. With increase in pyrolysis temperature, the adsorption capacity of biochar for NH4+-N and NO3--N was gradually weakened and gradually enhanced respectively. The adsorption process of ammonia nitrogen and nitrate nitrogen conformed to the Langmuir model and the fitted KL value was less than 1 indicating that the adsorption process was uniform monolayer adsorption and the adsorption of biochar was favorable adsorption. With increase in biochar application rate the leaching of NO3--N decreased having higher at 2.5 t ha-1 application rate followed by 5 t ha-1 and lower at 7.5 t ha-1. In packed soil column, the NH4+-N in leachate was maximum in T7 (18.6), followed by T4 (17.9), T13 (17.3) and minimum in T10 (17.2) at same application rate of manures and biochar. Finally, results also revealed that packed soil column performed better as compared with intact soil column to retain soil nutrient and hence, leaching potential of nutrient was less in packed column than intact soil column. In conclusion, biomass-derived biochar can enhance the amount of nutrient that is absorbed into the soil while decreasing the loss of nutrient from the soil in the form of ammonia and nitrate. To sum up, biomass-derived biochar can increase the adsorption amount of the nitrogen and reduce the loss of ammonia nitrogen and nitrate nitrogen in the soil, thus retaining the nitrogen.