Biochar Surface Research Articles

Removal of environmental pollutants using biochar: current status and emerging opportunities.

In recent times, biochar has emerged as a novel approach for environmental remediation due to its exceptional adsorption capacity, attributed to its porous structure formed by the pyrolysis of biomass at elevated temperatures in oxygen-restricted conditions. This characteristic has driven its widespread use in environmental remediation to remove pollutants. When biochar is introduced into ecosystems, it usually changes the makeup of microbial communities by offering a favorable habitat. Its porous structure creates a protective environment that shields them from external pressures. Consequently, microorganisms adhering to biochar surfaces exhibit increased resilience to environmental conditions, thereby enhancing their capacity to degrade pollutants. During this process, pollutants are broken down into smaller molecules through the collaborative efforts of biochar surface groups and microorganisms. Biochar is also often used in conjunction with composting techniques to enhance compost quality by improving aeration and serving as a carrier for slow-release fertilizers. The utilization of biochar to support sustainable agricultural practices and combat environmental contamination is a prominent area of current research. This study aims to examine the beneficial impacts of biochar application on the absorption and breakdown of contaminants in environmental and agricultural settings, offering insights into its optimization for enhanced efficacy.

Utilization of dragon fruit (Hylocereus undatus) peel-derived biochar for the adsorptive removal of tetracycline from aqueous solution

The peel of Hylocereus undatus was employed in the preparation of biochar and firstly applied for tetracycline removal from aqueous solution. Based on different characterization techniques, the material was found to possess a variety of surface functional groups on a porous structure and a pH point of zero charge (pHpzc) of 9.3. Adsorption of tetracycline (TC) was conducted under varying conditions, revealing significant effects of carbonization temperature, solution pH, adsorbent dose, ionic strength, contact time and initial concentration of TC on the biochar adsorption capacity. Kinetic data on TC adsorption were best described using the Elovich kinetic model, with an initial adsorption rate of 167.3 mg g−1 min−1. Isotherm data on adsorption of the desired biochar showed the best fit with the Temkin isotherm model, followed by the Langmuir model, displaying maximum adsorption capacity at 12.4 mg g−1. The electrostatic interactions between the charged biochar surfaces and certain fractions of TC were proposed as the major mechanism, together with H-bonding, pore-filling effect and π–π interaction. This study demonstrates great potential of H. undatus peel as a starting material to prepare an effective and reusable adsorbent in the removal of TC.

The electrochemical mechanism of biochar for mediating the product ratio of N2O/(N2O + N2) in the denitrification process

The biochar electrochemical properties and surface functional groups significantly impact N2O production and reduction during denitrification process. However, its effects on N2O emissions during the denitrification process and its electrochemical mechanisms remain unclear. The study examined the impact of pristine and oxidized biochar combined with two types of nitrogen fertilizers on the N2O/(N2O + N2) ratio and N2O emissions in an incubation experiment with seven treatments: (1) CK (no application of chemical fertilizer); (2) N1 (applying (NH4)2SO4); (3) N1B ((NH4)2SO4 + pristine biochar); (4) N1BO ((NH4)2SO4 + oxidized biochar); (5) N2 (applying KNO3); (6) N2B (KNO3 + pristine biochar); (7) N2BO (KNO3 + oxidized biochar). The study found that in comparison with applying nitrogen fertilizer alone, combining pristine biochar decreased soil N2O concentration by 7.1 %–85.8 %, while combining oxidized biochar increased it by 15.7 %–125.6 %. Applying pristine biochar reduced N2O/(N2O + N2) ratio by 10.4 %–86.2 %, whereas applying oxidized biochar increased it by 12.9 %–121.6 %. The application of pristine biochar increased the nosZ gene abundance and decreased the (nirS + nirK)/nosZ ratio, which contributed to reducing N2O to N2. Compared with oxidized biochar, the oxygen-containing functional groups of pristine biochar decreased by 46.6 %, and it possessed a higher specific surface area (23.01 m2 g−1) and electrical conductivity (0.003 mS cm−1). The correlation analysis showed that DOC and inorganic nitrogen were the key environmental factors affecting N2O emissions. Additionally, the electrical conductivity, specific capacitance, and oxygen-containing functional groups of the biochar were identified as the main factors driving N2O emissions. The SEM analysis suggested that the indirect influence of biochar electrochemical properties on N2O emissions was greater than its direct influence. Our work provides fresh perspectives on reducing soil N2O emissions and establishes a theoretical foundation for the subsequent preparation of biochar materials with enhanced N2O reduction capabilities.

Advanced carbo-catalytic degradation of antibiotics using conductive polymer-seaweed biochar composite: Exploring N/S functionalization and non-radical dynamics

Polyaniline (PANI) and Saccharina Japanica seaweed (kelp) biochar (KBC) composites were synthesized in-situ through polymerization. This study presents a novel approach to the degradation of sulfamethoxazole (SMX), a prevalent antibiotic, using a PANI-KBC composite to activate peroxymonosulfate (PMS). Extensive characterizations of the PANI-KBC composite were conducted, resulting in successful synthesis, uniform distribution of PANI on the biochar surface, and the multifunctional role of PANI-KBC in SMX degradation. A removal efficiency of 97.24% for SMX (10 mg L−1) was attained in 60 min with PANI-KBC (0.1 g L−1) and PMS (1.0 mM) at pH 5.2, with PANI-KBC showing effectiveness (>92%) across a pH range of 3.0–9.0. In the degradation of SMX, both radical (SO4•− and •OH) and non-radical (1O2 and electron transfer) pathways are involved. The reaction processes are critically influenced by the roles of SO4•−, 1O2 and electron transfer mechanisms. It was suggested that pyrrolic N, oxidized sulfur (−C−SO2−C−), structural defects, and O−CO were implicated in the production of 1O2 and electron transfer processes, respectively, and a portion of 1O2 originated from the conversion of O2•−. The study evaluated by-product toxicity, composite reusability, and stability, confirming its practical potential for sustainable groundwater remediation.

Time-varying contributions of FeII and FeIII to AsV immobilization under anoxic/oxic conditions: The impacts of biochar and dissolved organic carbon

Engineering black carbon (e.g. biochar) has been widely found in natural environments due to natural processes and extensive applications in engineering systems, and could influence the geochemical processes of coexisting arsenic (AsV) and FeII, especially when they are exposed to oxic conditions. Here, we studied time-varying kinetics and efficiencies of AsV immobilization by solid-phase FeII (FeIIsolid) and FeIII (FeIIIsolid) in FeII-AsV-biochar systems under both anoxic and oxic conditions at pH 7.0, with focuses on the effects of biochar surface and biochar-derived dissolved organic carbon (DOC). Under anoxic conditions, FeII could rapidly immobilize AsV via co-adsorption onto biochar surfaces, which also serves as the dominant pathway of AsV immobilization at the initial stage of reaction (0–5 min) under oxic conditions at high biochar concentrations. Subsequently, with increasing biochar concentrations, FeIIIsolid precipitation from aqueous FeII (FeIIaq) oxidation (5–60 min) starts to play an important role in AsV immobilization but in decreased efficiencies of AsV immobilization per unit iron. In the following stage (60–300 min), FeIIsolid oxidation is suppressed and leads to AsV release into solutions at >1.0 g·L−1 biochar. The decreasing efficiency of AsV immobilization over time is attributed to the gradual release of DOC into solution from biochar particles, which significantly inhibit AsV immobilization when FeIIIsolid is generated from FeIIsolid oxidation in the vicinity of biochar surfaces. Specifically, 4.06 mg·L of biochar-derived DOC can completely inhibit the immobilization of AsV in the 100 μM FeII system under oxic conditions. The findings are crucial to comprehensively understand and predict the behavior of FeII and AsV with coexisting engineering black carbon in natural environments.

Polydopamine-modified biochar supported polylactic acid and zero-valent iron affects the functional microbial community structure for 1,1,1-trichloroethane removal in simulated groundwater

In-situ enhanced bioreduction by functional materials is a cost-effective technology to remove chlorinated hydrocarbons in groundwater. Herein, a novel polydopamine (PDA)-modified biochar (BC)-based composite containing nanoscale zero-valent iron (nZVI) and poly-l-lactic acid (PLLA) (PB-PDA-Fe) was synthesized to enhance the removal of 1,1,1-trichloroethane (1,1,1-TCA) in simulated groundwater with actual site sediments. Its impact on functional microbial community structure in system was also investigated. The typical characterizations revealed uniform dispersion of PLA and nZVI particles on the BC surface, being smoother after PDA coating. The composite exhibited a significantly higher performance on 1,1,1-TCA removal (82.38%, initial concentration 100 mg/L) than Fe-PDA and PB-PDA treatments. The diversity and richness of the microbial community in the composite treatment consistently decreased during incubation due to a synergistic effect between PLLA-BC and nZVI. Desulfitobaterium, Pedobacter, Sphaerochaeta, Shewanella, and Clostridium were identified as enriched genera by the composite through DNA-stable isotope probing (DNA-SIP), playing a crucial role in the bioreductive dechlorination process. All the above results demonstrate that this novel composite selectively enhances the activity of microorganisms with extracellular respiration functions to efficiently dechlorinate 1,1,1-TCA. These findings could contribute to understanding the responsive microbial community by carbon-iron composites and expedite the application of in-situ enhanced bioreduction for effective remediation of chlorinated hydrocarbon-contaminated groundwater.

The Potential Significance of Microwave-Assisted Catalytic Pyrolysis for Valuable Bio-Products Driven from Albizia Tree

The objective of this study is to investigate the feasibility of Na2CO3 and ZSM-5 as catalysts in the microwave pyrolysis of Albizia branches. An evaluation was conducted to determine the influence of power applied, experimental time, particle size, and catalysis type and ratio on the quality and quantity of pyrolysis products. Established methods such as GC-MS, FTIR, HHV, SEM, EDX, and BET were used to characterize the properties of bio-oil and biochar produced. The results demonstrated that using both catalyst types led to a substantial enhancement in biogas production. The improvement ranged from 5% to 41% with Na2CO3 and reached 45% with ZSM-5. At a lower power level of 300 W, the bio-oil yield augmented from 28% to 40% and 53% when using ZSM-5 and Na2CO3, respectively. The GC-MS analysis revealed that the utilizing of catalysts enhanced the levels of aromatic compounds, esters, and alcohols in bio-oil, along with an increase in the higher heating value (HHV) from 19.5 MJ/kg to 22 MJ/kg and 24.2 MJ/kg using Na2CO3 and ZSM-5, respectively. Moreover, the biochar's surface area and pore volume experienced a considerable rise, going from 0.5512 m2/g and 0.00011 cm3/g to a higher value of 115.2073 m2/g and 0.0774 cm3/g when treated with Na2CO3. The data indicated that both catalyst types enhanced the generation of CH4, and CO2 was lower with ZSM-5. The utilization of catalysts improves the quality of the biofuel produced and promotes the efficiency of the process in terms of energy consumption and processing time.

Optimization of activation by peroxidation and photo-assisted peroxidation of biochar produced from sewage sludge

Biochar from biomass, a cost-effective and sustainable alternative to pulverized activated carbon (PAC), often faces limitations in pore size and surface functionality. Hydrogen peroxide (H₂O₂) activation can enhance biochar's surface properties but requires large quantities and high concentrations, increasing production costs. Advanced oxidation methods, such as H₂O₂/UV radiation, can reduce H₂O₂ usage by generating highly reactive hydroxyl radicals (*OH). This study investigates biochar production from activated sewage biosolids using H2O2 activation and H2O2/UV radiation. Optimization was conducted via a central composite rotational design, varying activation parameters activation pH (1.5, 4.0, 7.0, 9.0, and 11.5) and H2O2 concentration (0, 10, 20, 30, and 40 vol), with methylene blue (MB) adsorption capacity as the metric. Characterization was performed using FTIR, SEM, EDS, XRD, and N2 adsorption/desorption techniques. Results indicated optimal biochar activation at pH 11.5 with 20 vol% H2O2. Activation pH was more significant than H2O2 concentration. Desirability curve analysis suggested that optimized parameters did not significantly enhance adsorption capacity, with desirability values at 93.053 %. Overall, H2O2 efficiently increased surface area by degrading the adsorbent, while H2O2/UV effectively removed impurities.

Properties and combustion characteristics of bioslurry fuels from agricultural waste pyrolysis

ABSTRACT The current research investigates the combustion characteristics of bioslurry fuel derived from the products of agricultural waste pyrolysis. The bioslurry fuel was prepared by mixing biochar and pyrolysis oil. The combustion characteristics of a suspended single droplet of the bioslurry were analysed. The results indicate that an increase in pyrolysis temperature (400–600°C) lead to higher concentrations of fixed carbon (56–60%), increased ash content (16–18%), and higher calorific values (25–32 MJkg−1). As the pyrolysis temperature rises, the biochar surface becomes more porous, lower volatile matter content and particle size. As biochar content increases, the bioslurry’s density, viscosity, and caloric value increase but stability index decreases. Higher biochar content in the bioslurry increases the ignition delay and burnout time while reducing the burning rate. The bioslurry fuel contained 30% biochar achieved a calorific value of 28 MJkg−1 and a viscosity of 600 cP, comparative to conventional fossil fuels. Highlights Up to 30% BC can be added to pyrolysis oil to produce SF. Pyrolysis temperature increased FC, ash, and calorific value of biochar. Biochar surface appears more porous with increasing pyrolysis temperature. Biochar content affects bioslurry combustion characteristics.

Cobalt-Modified Biochar from Rape Straw as Persulfate Activator for Degradation of Antibiotic Metronidazole

A cobalt-loaded magnetic biochar (Co-MBC) catalyst was synthesized to enhance the removal of metronidazole (MNZ). Study explored the performance and mechanism of MNZ degradation by Co-MBC activated permonosulfate (PMS). Results showed that cobalt oxides were effectively deposited onto the biochar surface, new oxygen functional groups were added to the modified biochar, and the presence of the metallic element Co enhanced the efficiency of PMS activation in the composite. More than 90% of MNZ was removed after 60 min with a catalyst dosage of 0.2 g/L and a PS concentration of 1 mM. After four reuses, Co-MBC still showed excellent catalytic performance to degrade over 75% of MNZ. The reaction system performed well even in the presence of inorganic anions and organic macromolecules. However, the degradation rate was inhibited under alkaline conditions. The quenching experiment indicated that •SO4−, •OH, 1O2, and •O2− synergistically degraded MNZ, and that•SO4− played a dominant role. LC-MS was applied to assess intermediate degradation products, in which CO2, H2O, and NO3− were the final degradation products, and potential degradation pathways were suggested. In conclusion, Co-MBC was an efficient and stable catalytic material, and its ability to activate PMS was improved to effectively degrade antibiotics, a typical priority pollutant.

Enhancing microplastics removal from soils using wheat straw and cow dung-derived biochars

Microplastics have attracted extensive public attention due to their harmful effects on environments and organisms, especially for small-size microplastics. Herein, six kinds of biochar were produced by wheat straw and cow dung at 500, 600 and 700 °C respectively for the removal of 1 μm polystyrene microplastics from soils. The removal efficiencies of microplastics exceeded 86% for all biochars. With increasing pyrolysis temperature, the removal performance of wheat straw biochars for microplastics gradually improved, while the removal efficiency of cow dung biochars decreased. Biochars effectively trapped microplastics within their channels, oxygen-containing functional groups (CO32− and COO−) on the surface of biochars facilitated the adsorption of microplastics. After seven cycles of biochars recycling, the removal performance of microplastics remained above 85%, the removal process was primarily governed by the adsorption sites rather than the porous structure of biochars. This article provided eco-friendly and recyclable biochar materials for microplastics removal and technical support for addressing soil microplastics pollution.

Adsorptive removal of phosphate from water with biochar from acacia tree modified with iron and magnesium oxides

A novel biochar (BC) from Acaciatortilis trees pruning waste was synthesized and tested for the removal of phosphate from aqueous solutions. The BC was prepared by calcination at 600 °C and doped with Fe3O4 and MgO by hydrothermal process. The presence of iron and magnesium ions in the modified BC was confirmed by EDS analysis and X-ray diffraction (XRD) methods. Both unmodified and doped BCs were tested for phosphate removal from synthetic 1–500 ppm aqueous solutions. While the unmodified BC did not show any significant removal of phosphate from aqueous solutions, the modified BC almost completely removed phosphate from water. The enhancement in removal efficiency is due to an increase in the overall surface charge and surface area of BC as a result of doping with Fe3O4 and MgO salts. The average porosity and BET surface area corresponding to the plain BC increased by more than 20% from 322 to 394 m2/g after modification by impregnation with iron oxide and magnesium oxide. The modificaiton of BC with Fe3O4 and MgO nanoparticles was observed to increase the point of zero electric charge (PZC) from pH 3.4 (corresponding to plain BC) to pH 5.3 (corresponding to modified BC). The adsorption process was very fast and a phosphate removal value of 82.5% was reached only after 30 min of adsorption, while the removal efficiency after 4 h of adsorption was 97.5%. The rapid removal efficiency in short contact time is attributed to the high surface area of BC and strong bonding between the modified BC surface and PO43− ions. The highest adsorption capacity was observed to correspond to 98.5 mg/g which was achieved at PO43− concentration of 500 ppm and pH 8.5. Moreover, after fitting the adsorption data onto four of the most widely used adsorption isotherm models, the adsorption of PO43− onto BC can be better described by the Langmuir isotherm model.

Mechanistic insight into the effects of interaction between biochar and soil with different properties on phenanthrene sorption

Soil composition varies considerably in nature, so it is vital to investigate the mechanism of the effect of various soil parameters on biochar sorption capacity. In this study, two biochars (W4 and W7) were derived from wheat straw at temperatures of 400 and 700 °C and were incubated with three different soils. Changes in biochar surface features by aging in the soils and the consequent impact on phenanthrene sorption were examined. The results showed that the effect of adding biochar on phenanthrene sorption capacity (Koc) varied by soil. When biochar was freshly mixed with soil, the Koc value in soil with higher clay content was more dramatically altered by biochar, which is due to clay particles adhering to the biochar surface. Moreover, the Koc value was significantly decreased by the addition of W4 but increased by the addition of W7 in general. After aging, most of the Koc value decreased. The greatest decrease in Koc value was observed in biochar and soil composed with the highest clay content for W4 (24–63%), as well as soil composed with the highest organic matter content for W7 (46–64%). This is because the surface polarity and micropores of biochar dropped the most rapidly in these mixes, resulting in a significant decrease in hydrophobic and pore-filling properties. The results revealed that the impact of biochar-soil interactions on phenanthrene sorption is related to not only biochar properties but also soil clay particles, soil organic matter content and pH. The findings of the study can be utilized to assess the efficacy of biochar application in soil remediation for various features.

Biochar/poly(aniline-pyrrole) modified graphite electrode and electrochemical behavior for application in low-cost supercapacitor

An attempt is made to use biochar (BC), a carbon rich low-cost green material, as a platform to house conducting polymer for fabricating stable graphite electrodes for application in next generation supercapacitor devices. Here, BC is first prepared from sucrose solution using a simple hydrothermal method. The seeded chemical oxidative copolymerization of aniline and pyrrole is then carried out at identical comonomer weight ratio using BC as seed particles. Two different BC to mixed monomer (w/w) ratios (1:0.7 and 1:1) have been used and the prepared composites are named as BC/P(Ani-Py)1:0.7 and BC/P(Ani-Py)1:1 respectively. Independent of composition, both BC seed and composite particles are spherical. The smooth homogeneous surface of BC turned heterogeneous after composite formation. The average size of BC seed particles is 2.56 µm and those of composites prepared at weight ratios of 1:0.7 and 1:1.0 are 2.72 and 2.90 µm respectively. Cyclic voltammetry (CV), galvanostatic charging discharging (GCD), and electrochemical impedance spectroscopy (EIS) are used to evaluate the electrochemical properties. Comparatively, the BC/P(Ani-Py)1:1 composite modified graphite electrode exhibited the highest capacitance value (274.27 F g−1 at a current density of 1.0 A/g) and is capable of acting as a supercapacitor electrode. A long-term cycling test of the BC/P(Ani-Py)1:1 modified electrode at a current density of 5.0 A/g displayed a capacitance retention of 96.6 % after 1000 cycles of charge and discharge, indicating a very good cycle stability.

An Effective Biochar Application for Reducing Nitrogen Emissions from Buffalo Digestate Storage Tank

Open manure storage contributes to the release of ammonia (NH3) into the atmosphere. Tank floating covers represent an effective technique to reduce NH3 emissions and biochar has been gain attention as a floating cover and as manure additive. Nevertheless, the mechanisms involved in the process still need to be elucidated since they are influenced by the biochar specific properties, application methods and dose. This work aims to study: (i) the biochar adsorption performances in an NH3 aqueous solution under conditions relevant to manure storage and (ii) the effect of different biochar application methods and dosage on NH3 emissions from buffalo digestate storage. The results show that a 43% reduction in NH3 emissions can be achieved by using biochar as a floating cover of 2 cm rather than as an additive. Moreover, the results show that the biochar produced at 550 °C acts as an adsorbent material for both NH4+ and NH3, by being adsorbed on the biochar surface in the form of NH4+ after H+ abstraction from the acid groups. A minimum cover height of 2 cm is required to give compactness and provide an additional resistance to the gas transfer, which is even more relevant than the adsorption in reducing NH3 emissions.

N/O-Codoped Ultrathin Porous Biochar Derived from Casein for Fast Adsorption of Iodine.

The release of radioactive iodine into the environment poses a significant threat, as it can contaminate soil, water, and food chains, leading to detrimental effects on ecosystems and biodiversity. Hence, employing the adsorption method proves to be a simple yet effective approach for treating radioactive waste. N/O-codoped ultrathin porous biochar, synthesized from casein using NaHCO3 activation, emerges as a potential candidate for adsorption materials. The saturation level of I2 adsorption in 100 mg L-1 iodine-cyclohexane solution is 73 mg·g-1 at 20 min. The density functional theory (DFT) calculations and experiments attribute this phenomenon to the presence of graphite nitrogen (NG) and C-OH groups on the biochar surface. Furthermore, the pseudo-first-order model fits better with the experimental values, suggesting that the adsorption of iodine by the adsorbent is primarily physisorption-based. The Freundlich isotherm is suitable for iodine adsorption of biochar, owing to the abundance of adsorption sites within the porous structure, particularly at the edges, which enhance the adsorption activity. Significantly, the study highlights that NG adsorptive sites exhibit 1.5 times higher adsorption activity compared to C-OH adsorptive sites, underscoring the essential role of NG in iodine adsorption for electron transfer. Overall, these findings underscore the potential of N/O-codoped ultrathin porous biochar in effectively mitigating the presence of radioactive I2, showcasing its promise in addressing environmental challenges associated with radioactive contamination.

Improving biochar properties through liquid-phase exfoliation of onion peel biochar doped with chicken feathers

In recent decades, heightened environmental awareness has spurred a global push for innovative waste-to-wealth solutions. This study explores liquid-phase exfoliation as a strategy to enhance biochar properties. By doping onion peels and chicken feathers, hybrid biochar (HBC) was produced using a low-temperature co-carbonization system. Two exfoliation routes, the nitric acid and acetone routes, were compared with the un-exfoliated HBC through material characterization. Material characterization revealed distinct morphological features and a range of functional groups being introduced by exfoliation. It was also observed through the BET analysis that the HBC samples are mesoporous, with the exfoliated HBCs having an enhanced surface area and pore volume. Elemental analysis showcased HBC's fortification, highlighting potential applications such as adsorbents and soil amendments. This investigation shows the efficacy of liquid-phase exfoliation in enhancing biochar surface characteristics, opening avenues for diverse applications.

Selective adsorption of antibiotics from human urine using biochar modified by dimethyl sulfoxide, deep eutectic solvent, and ionic liquid

Antibiotics present in human urine pose significant challenges for the use of urine-based fertilizers in agriculture. This study introduces a novel two-stage approach utilizing distinct biochar types to mitigate this concern. Initially, a modified biochar selectively adsorbed azithromycin (AZ), ciprofloxacin (CPX), sulfamethoxazole (SMX), trimethoprim (TMP), and tetracycline (TC) from human urine. Subsequently, a separate pristine biochar was employed to capture nutrients. Biochar, derived from sewage sludge and pyrolyzed at 550 and 700 °C, was modified using dimethyl sulfoxide, deep eutectic solvent, and ionic liquid to enhance antibiotic removal in the first stage. The modifications introduced hydrophilic functional groups (-OH/-COOH), which favor antibiotic adsorption. Adsorption kinetics followed the pseudo-second-order model, with the Langmuir isotherm model best describing the adsorption data. The maximum adsorption capacities for AZ, CPX, SMX, TMP, and TC after the modification were 196.08, 263.16, 81.30, 370.37, and 833.33 μg/g, respectively. Pristine biochar exhibited a superior ammonia adsorption capacity compared to the modified biochar. Hydrogen bonding, electrostatic attraction, and chemisorption drove antibiotic adsorption on the modified biochar. Regeneration efficiency declined due to solvent accumulation and potential byproduct formation on the biochar surface (<30% removal capacity after three cycles). This study presents innovative biochar modification strategies for selective antibiotic adsorption, laying the groundwork for environmentally friendly urine-based fertilizers in agriculture.

Synergistic effect of adsorption and photolysis on methylene blue removal by magnetic biochar derived from lignocellulosic biomass

In this study, magnetic biochar was synthesized by doping Fe3O4 onto the biochar surface followed by analysis of its properties. The efficiency of methylene blue (MB) removal through the combined processes of adsorption and photolysis was assessed. The presence of Fe3O4 on the biochar surface was confirmed using Raman spectroscopy and X-ray photoelectron spectroscopy. The magnetic biochar, after MB adsorption, showed a magnetism of 39.50 emu/g leading to a 97.07 % recovery rate. The specific surface area of biochar was higher (380.68 m2/g) than that of magnetic biochar (234.46 m2/g), and the maximum adsorption capacity of MB was higher in the biochar (0.03 mg/g) than that in magnetic biochar (0.02 mg/g) under the optimal conditions for MB adsorption. The MB adsorption experiments using biochar or magnetic biochar were optimally conducted under 10–20 mg/L MB concentration, 1 g biochar dosage, pH 12, 200 rpm rotation speed, 25 °C temperature, and 30 min duration. Under dark conditions, biochar had a higher MB removal rate, at 83.91 %, compared to magnetic biochar, at 78.30 %. Under visible light (λ > 425 nm), magnetic biochar effectively removed MB within 10 min, highlighting the synergistic effect of adsorption and photolysis. MB is physically and chemically adsorbed by the monolayer on the surface of EB and EMB according to adsorption behavior.

Preparation of magnetic coconut clothing biochar for extracting neonicotinoid insecticides from environmental water samples

In this study, the magnetic coconut clothing biochar hybrid materials were successfully prepared by in-situ method. The obtained magnetic biochar was characterized in detail by using series of analytical techniques. The results showed that the magnetic hybrid materials presented alveolate network structures with abundant large pores and good magnetic separation ability with Fe3O4 nanoparticles obviously attached on the surface of biochar. The magnetic biochar hybrid materials were used as adsorbents during magnetic solid-phase extraction process for extracting neonicotinoid insecticides from environmental water samples. The adsorption and desorption parameters (adsorption time, elution condition, sample volume, sample pH) affecting magnetic solid-phase extraction efficiency were carefully investigated. Under the optimum conditions (adsorption for 15 min, 5 % formic acid-acetonitrile as elution condition, 50 mL of sample volume, 15 mg of magnetic biochar, pH at 5.0), the magnetic solid-phase extraction process based on magnetic coconut clothing biochar hybrid materials coupled with high performance liquid chromatography tandem mass spectrometry for enriching and detecting neonicotinoid insecticides in environmental water samples was established. The good linear relationship in the range of 0.5–200 ng mL−1 with correlation coefficients greater than 0.9989 and the lower limits of detection (0.0017–0.0069 ng·mL−1) were obtained. The recovery in the spiked water samples was in the range of 68.6 %-104.0 % with relative standard deviation from 0.4 % to 9.3 %. These results demonstrated that the established method was highly sensitive, convenient and repeatable for directly analyzing trace neonicotinoid insecticides in environmental water samples. More importantly, the novel biochar from coconut clothing was introduced into sample pretreatment to enrich trace organic pollutants.