Magnetic Biochar Research Articles

Comparative study of organic removal by pre-adsorption oxidation and synchronous adsorption oxidation processes: Performance and mechanism

Both adsorption and oxidation occur and contribute to organics removal in carbonaceous materials based advanced oxidation processes, while the correction of adsorption and oxidation, and the role of adsorption in the veritable removal of organic are not clear. Herein, we investigated the performance of carbamazepine (CBZ) removal by peroxymonosulfate (PMS) activated by magnetic Fe-doped biochar through two models of pre-adsorption oxidation and synchronous adsorption oxidation processes. The adsorption process was better fitted by pseudo-second-order kinetic model and the adsorption mechanism was obtained by comprehensive analysis of equilibrium adsorption capacities, surface functional groups, specific surface area, pore volume, and ID/IG value. It is noted that pre-adsorption highly inhibited the further oxidation of CBZ in 0.5Fe@LSBC700/PMS system due to the occupied catalytic active sites. Total CBZ removal in pre-adsorption oxidation (45 %) was inferior to synchronous adsorption oxidation (∼100 %), as well as the veritable CBZ oxidation removal of 27 % for pre-adsorption oxidation vs ∼100 % in synchronous adsorption oxidation at 30 min. Oxidation degradation of CBZ based on radical oxidation was identified by quenching experiments and electron paramagnetic resonance measurements. This work is conducive to identifying the role of adsorption during the removal of organics in the adsorption-oxidation process, as well as veritable adsorption and oxidation removal of organics.

Efficient synthesis of magnetic activated carbon from oak pericarp for enhanced dye adsorption: A one-step approach

This study presents a one-step synthetic method utilizing oak pericarp treated with FeCl3 and ZnCl2 as a precursor for the production of magnetic activated carbon (MAC). Characterization techniques including FTIR, SEM-EDX, TGA, XRD, VSM, BET, and pHpzc confirm the integration of biochar characteristics and magnetic properties of iron oxides in the MAC composite. Batch adsorption tests investigate the adsorption capacity of Rhodamine B (RhB) and Rose Bengal (RB) dyes by MAC under varied conditions, including adsorbent dose, contact time, solution pH, ionic strength, temperature, and initial dye concentration. Optimal adsorption conditions for RhB and RB are identified at pH 2 and 7, with adsorbent doses of 0.75 g/L and 1 g/L, and equilibrium times of 180 min and 120 min, respectively. Adsorption isotherm models (Langmuir, Freundlich, and Temkin) are employed, with the Freundlich model providing the best fit. MAC demonstrates a maximum monolayer adsorption capacity of 198.529 mg.g−1 for RhB and 42.551 mg.g−1 for RB at 20 °C. Kinetic data align with the pseudo-second-order model, and thermodynamic parameters confirm the spontaneous and endothermic nature of the adsorption process. In conclusion, this study successfully synthesizes magnetic biochar with enhanced efficacy in dye adsorption. The one-step method proves efficient for treating industrial dye effluents, as evidenced by batch desorption studies over four cycles, establishing the reusability of the MAC.

Transesterification of used cooking oil by palm lignocellulosic biomass magnetic biochar catalyst: Optimization and kinetic analysis

Biodiesel has recently gained popularity as an alternative biofuel to substitute fossil fuel. Utilization of magnetic biochar catalyst (MBC) in biodiesel production can enhance the catalyst separation process. In this research, MBC was synthesized from oil palm waste such as palm kernel shell (PKS), oil palm frond (OFP), and empty fruit bunch (EFB). Biodiesel production parameters were studied using the Central Composite Design-based Response Surface Method. Based on the characterization results, EFB is the most suitable palm lignocellulosic biomass for MBC synthesis. The MBC has a BET surface area of 44.42 m2 g−1, an average acid density value of 3.85 mmol g−1, and a σs value of 3.19 Am2 kg−1. MBC synthesis is at its optimal by using 1.5 M FeCl3·6H2O solution, 800 °C carbonization temperature, and 2.5 M H2SO4. The optimized transesterification parameters are: catalyst loading of 10.25 wt%, methanol to oil molar ratio of 28, 70 °C, and 8 h gave a maximum fatty acid methyl ester yield of 91.50 %. After five cycles, the yield dropped to 67.37 %. Biodiesel production is reported to be the pseudo-irreversible first-order kinetic with an activation energy of 29.20 kJ mol−1. The physicochemical characterization showed the biodiesel has met the ASTM D6751 standard.

Removal of Pb pollution using alginate-coupled magnetic sludge biochar: Solidification and stabilization behavior and electron promotion mechanisms

Environmental and human health problems caused by Pb pollution have attracted much attention, and solidification and stabilization are effective means for its remediation. Improving the ability of biochar to remediate heavy metals through modification is the focus of current biochar research. This study used calcium-alginate gel (GB) and Fe3+ (magnetic) to encapsulate and improve sludge biochar (SB), and explored the adsorption behavior and passivation mechanism of Pb2+ on it from outside to inside. The magnetic-biochar (MB) in magnetic-biochar-gel microspheres (MBGB) showed a homogeneous dispersion and part of the Fe ion was detached from the MB into the three-dimensional pores of the gel. The results of kinetic, isothermal and pH adsorption experiments showed that the MBGB has 108.4 % and 200 % higher Pb2+ adsorption capacity and rate than SB and can be applied to pH 3–9. The adsorption of Pb2+ by MBGB is a multilayer adsorption with both physical and chemical mechanisms. Mineralogical and electrochemical results demonstrate that the cross-linking of the gel with magnetic-biochar (MB) can provide a directional diffusion channel for Pb2+ from the outside to the inside. The electron transfer rate of MBGB was significantly higher than that of SB (222.2 %) after the reaction. The dissolved cations and electrons on the MB guide Pb2+ from the MBGB surface to the internal MB quickly via accelerating the electron transfer and migration rate between Pb2+ and MB. Subsequently, the abundance of PO43− on the MB ensures stable mineral precipitation (Pyromorphite). Moreover, four-step extraction analysis confirmed that most of Pb2+ in MBGB was stable (36.2 % acid-soluble and 47.6 % non-bioavailable). Meanwhile, the Pb adsorption efficiency of MBGB was still >93.0 % after three cycles of adsorption-desorption. Excellent reuse performance and stability guarantee the environmental security of MBGB. The results of the study provide theoretical support for the efficient treatment of Pb2+ polluted water assisted by gel materials.

RETRACTED: Sun et al. Study on the Removal Efficiency and Mechanism of Tetracycline in Water Using Biochar and Magnetic Biochar. Coatings 2021, 11, 1354

The Coatings Editorial Office retracts the article entitled “Study on the Removal Efficiency and Mechanism of Tetracycline in Water Using Biochar and Magnetic Biochar” [...]

Adsorptive removal of perfluorooctanoic acid from aqueous matrices using peanut husk-derived magnetic biochar: Statistical and artificial intelligence approaches, kinetics, isotherm, and thermodynamics

Removal of perfluorooctanoic acid (PFOA) from water matrices is crucial owing to its pervasiveness and adverse ecological and human health effects. This study investigates the adsorptive removal of PFOA using magnetic biochar (MBC) derived from FeCl3-treated peanut husk at different temperatures (300, 600, and 900 °C). Preliminary experiments demonstrated that MBC600 exhibited superior performance, with its characterization confirming the presence of γ-Fe2O3. However, efficient PFOA removal from water matrices depends on determining the optimum combination of inputs in the treatment approaches. Therefore, optimization and predictive modeling of the PFOA adsorption were investigated using the response surface methodology (RSM) and the artificial intelligence (AI) models, respectively. The central composite design (CCD) of RSM was employed as the design matrix. Further, three AI models, viz. artificial neural network (ANN), support vector machine (SVM), and adaptive neuro-fuzzy inference system (ANFIS) were selected to predict PFOA adsorption. The RSM-CCD model applied to optimize three input process parameters, namely, adsorbent dose (100–400 mg/L), pH (3–10), and contact time (20–60 min), showed a statistically significant (p < 0.05) effect on PFOA removal. Maximum PFOA removal of about 98.3% was attained at the optimized conditions: adsorbent dose: 400 mg/L, pH: 3.4, and contact time: 60 min. Non-linear analysis showed PFOA adsorption was best fitted by pseudo-second-order kinetics (R2 = 0.9997). PFOA adsorption followed Freundlich isotherm (R2 = 0.9951) with a maximum adsorption capacity of ∼307 mg/g. Thermodynamics and spectroscopic analyses revealed that PFOA adsorption is a spontaneous, exothermic, and physical phenomenon, with electrostatic interaction, hydrophobic interaction, and hydrogen bonding governing the process. A comparative analysis of the statistical and AI models for PFOA adsorption demonstrated high R2 (>0.99) for RSM-CCD, ANN, and ANFIS. This research demonstrates the applicability of the statistical and AI models for efficient prediction of PFOA adsorption from water matrices using MBC (MBC600).

Application of recyclable iron-based supplementation for promoting biohydrogen and ethanol co-production

Supplementation additives is a promising approach in enhancing hydrogen production during fermentation processes, owing to the advantages of simple operation and low energy consumption. Exploring efficient and recyclable additives is a pivotal issue for its industrial applications. In this study, a magnetic recyclable iron-based biochar (FeBCs) was synthesized by one-step co-pyrolysis of straw biomass and K2FeO4 to enhance hydrogen production of Ethanoligenens harbinense. Results showed that the biochar derived by pyrolysis at 1000 °C (FeBC1000) established the highest H2 yield (2.09 mol·H2/mol·glucose) and ethanol yield (82.35 ± 3.27 mM) being 41.21 % and 22.27 % higher than that of the control group, respectively. The addition of FeBCs facilitated the substrate consumption and the excretion of protein and carbohydrate in extracellular polymeric substance (EPS). Magnetic FeBC1000 displayed the remarkable reusability, and the H2 yield was 33.59 % higher than that of the control group after being recycled for three times. The mechanism of FeBC1000 enhancing hydrogen production was that it promoted hydrogenase activity by reducing the redox potential, enhancing electron transfer, buffering the pH, releasing ferrous ions, and promoting cell immobilization. Overall, the study provided a recyclable and efficient magnetic additive for biohydrogen production, and operate a new direction for comprehensive utilization of straw with low energy input.

Coupled capture and photocatalysis of g-C3N4 based magnetic composites: Mechanism and disinfection activity against Staphylococcus aureus

The disinfection ability of g-C3N4 by photocatalysis is restricted, owing to its small surface area and rapid combination of holes (h+) and electrons (e−). Moreover, recycling of g-C3N4-based photocatalysts from aqueous solution is difficult, which increases the cost of application. In the present study, g-C3N4 was combined with magnetic biochar (MBC) by high temperature calcination to fabricate g-C3N4/MBC composites. The as-prepared g-C3N4/MBC composites acquired larger specific surface area, narrow bandgap, and broad-range of visible absorption capability. The g-C3N4/MBC composites showed good killing efficiency towards Staphylococcus aureus (S. aureus) under visible light irradiation. Efficient photocatalysis was achieved by the effective separation of e−/h+ within the g-C3N4/MBC composites. Moreover, the capture effect of MBC for S. aureus reduced the distance and increased the contact area between the g-C3N4/MBC composite and S. aureus. The g-C3N4/MBC-10 % showed notable stability and reusability over a broad pH range of 4–8 and in presence of different inorganic ions (Cl− and SO42−) and humic acid. After 5 cycles, the g-C3N4/MBC-10 % could still eliminate about 95 % of S. aureus cells. The g-C3N4/MBC-10 % was also highly effective in reducing the bacterial population in water samples taken from a nearby lake, thus showing considerable promise for use in water sterilization. In addition, g-C3N4/MBC composites were highly effective in eliminating the biofilm and inhibiting the growth of the new biofilm of S. aureus. The main active species in photocatalytic disinfection were determined, to be •OH, h+, and •O2−. This study would help to understand the capture and photocatalysis of g-C3N4 based composites for environmental applications.

A turbidity-based study of removing polyvinyl chloride nanoplastics using magnetic biochar

Magnetic biochars (MBCs) can quickly and efficiently remove polystyrene nanoplastics (NPs) from water. However, the removal efficiency of other types of NPs by different MBCs remains unknown. In this study, the removal performance of polyvinyl chloride NPs (PVC-NPs) by magnetic corncob biochar (MCCBC) and magnetic walnut shell biochar (MWSBC) was evaluated by measuring turbidity. The results indicate rapid adsorption of PVC-NPs onto MCCBC and MWSBC, reaching equilibrium within 1 h. The removal efficiencies of PVC-NPs by MCCBC and MWSBC were 94% and 92%, respectively. The relatively higher PVC-NPs removal capacity by MCCBC resulted from the greater amount of iron oxide on its surface, creating a rougher surface. The presence of monovalent ions (K+, Na+, Cl-, NO-3) promoted the removal of PVC-NPs by MWSBC, but caused a reduction in the adsorption of PVC-NPs on MCCBC. In contrast, divalent ions (Mg2+, Ca2+, and SO2-4) significantly inhibited the removal efficiency of PVC-NPs by competing for adsorption sites on MBCs (p < 0.01). Increasing the ionic strength inhibited the removal efficiency of PVC-NPs by MBCs. In addition, the highest removal efficiency of PVC-NPs was obtained at pH 5.0–7.0. Apart from adsorbing onto the surface of MBCs and becoming trapped within their pores, PVC-NPs can be magnetized by iron oxides. Moreover, PVC-NPs could aggregate with the small fragments of MBCs, thus allowing for easy removal by a magnet. The results provide new insight into the investigation of techniques to remove NPs other than PS from water.

Novel magnetic N-doped biochar derived from sugarcane bagasse and red mud for effective adsorption of tetracycline hydrochloride

In this work, with sugarcane bagasse (SB) and red mud (RM) as raw materials, magnetic nitrogen (N)-doped biochar (MNSB) was synthesized by a facile one-pot pyrolysis method and then applied as an efficient adsorbent to remove tetracycline hydrochloride (TC-HCl) from wastewater. The results of SEM, EDS, VSM, BET, FT-IR, and XPS demonstrated that the synthesized MNSB adsorbent had a large specific surface area, excellent superparamagnetic properties, and rich mesopore pore structures. The batch adsorption experiments revealed that the TC-HCl could be removed 96.3% with the optimal adsorption conditions: MNSB dosage of 0.25 g/L, initial pH of 6.58, TC-HCl initial concentration of 20 mg/L, and adsorption temperature of 30 °C. The analysis of adsorption kinetics and isotherms showed that the adsorption process was mainly controlled by chemisorption, and the theoretical maximum adsorption capacity of TC-HCl on MNSB was 143.9 mg/g. Mechanistic analysis revealed that the excellent adsorption process of MNSB for TC-HCl was mainly contributed by pore filling, π–π interaction, hydrogen bonding, and electrostatic attraction. The recycling and settlement experiments demonstrated that MNSB had good stability and settleability. This study successfully opened new prospects that utilizing RM and SB to prepare a low-cost adsorbent to remove TC-HCl from water.

Novel chitosan-modified biochar prepared from a Chinese herb residue for multiple heavy metals removal: Characterization, performance and mechanism

In this study, the sorption properties of Cr(VI), As(III), and Pb(II) on chitosan-modified magnetic biochar (CMBC) derived from residues of Ligusticum chuanxiong Hort. were investigated. CMBC was found to be a valuable material for removing three heavy metals from water simultaneously. Kinetic analysis suggested Cr(VI), As(III), and Pb(II) were chemisorbed onto CMBC, while isotherm data conformed well to Langmuir model, the maximum adsorption capacity of CMBC was found to be 65.74 mg/g for Cr(VI), 49.32 mg/g for As(III), and 69.45 mg/g for Pb(II). Experiments, characterization, and density functional theory (DFT) calculations were employed to explore the mechanisms. Furthermore, CMBC demonstrated excellent removal rates of over 95% for Cr(VI), 99% for As(III) and Pb(II) from contaminated water bodies. This work shows that CMBC holds significant potential for wastewater treatment of heavy metals and provides an effective solution for the utilization of Chinese herb residues in environmental remediation.

Aquatic invasive plant biomass-derived magnetic porous biochar prepared by sequential carbonization and coprecipitation for diethyl phthalate removal from water

Low-cost multifunctional sorbents are urgently needed, especially for the treatment of emerging pollutants that are widely distributed in various water environments. This work transformed an aquatic invasive plant, Pistia stratotes, into magnetic porous biochars (P-MPBs) based on a proposed strategy involving sequential carbonization to increase porosity and subsequent coprecipitation with ferric salts. Both the porous structure (specific surface area of up to 996.86 m2/g) and high Fe3O4 loading (saturation magnetization of up to 23.48 emu/g) were maintained. A typical plasticizer, diethyl phthalate (DEP), was selected as a model emerging organic pollutant, and the sorption quantity of the P-MPBs reached 490.04 mg g−1, which is much higher than that of many reported sorbents, especially magnetic sorbents. P-MPBs can be reused multiple times due to their excellent separation characteristics and stable structure. On the basis of kinetics and isotherm analysis, multilayer sorption, including pore filling, hydrogen bonding, π–π stacking, and partitioning, was the main DEP sorption process for the P-MPBs. Our study suggested that the proposed method could be promising and inspiring for the transformation of biowaste into excellent magnetic porous biochar that is recyclable and highly efficient at removing pollutants in water.

Activation of peracetic acid by a magnetic biochar-ferrospinel AFe2O4 (A = Cu, Co, or Mn) nanocomposite for the degradation of carbamazepine − A comparative and mechanistic study

Peracetic acid (PAA)-based advanced oxidation processes (AOPs) are promising technologies for the efficient treatment of persistent contaminants in wastewater. In this study, three different magnetic biochar (BC)-ferrospinel AFe2O4 (A = Cu, Co, or Mn) nanocomposites were synthesized through a combined sol–gel/pyrolysis process for the activation of PAA to degrade carbamazepine (CBZ). The following order of efficiency was observed for CBZ degradation in the presence of PAA: BC-CoFe2O4 (100 %) > BC-MnFe2O4 (7 %) ≈ BC-CuFe2O4 (7 %). In addition, 0.8 mM PAA, 0.3 g/L catalyst, nearly neutral pH, and 333 K were identified as the optimal operating parameters for the degradation of 1 mg/L CBZ in the BC-CoFe2O4/PAA system. Mechanistic studies revealed that CH3C(O)OO radicals are the dominant active species for the degradation of CBZ in the BC-CoFe2O4/PAA system, and the continuous conversion of Co(II) to Co(III) in this system is responsible for the generation of these radicals. In addition, the water matrices (e.g., humic acid (20 mg/L), NaCl (0.05 M), and NaNO3 (0.01 M)) played negligible roles in the degradation of CBZ in the BC-CoFe2O4/PAA system. This system exhibited highly selective and reactive degradation of organic pollutants with electron-rich groups (e.g., CBZ (0.36 min−1), sulfamethoxazole (0.12 min−1), and diclofenac (0.28 min−1)). Furthermore, the degradation products of CBZ were identified, and possible degradation pathways and toxicity of these transformation products were proposed. The BC-CoFe2O4/PAA system demonstrated outstanding degradation performance in dynamic systems and real wastewater treatment applications. This study describes the performance of an efficient and easy-to-separate catalyst for the activation of PAA. This study facilitates the development and application of PAA-based AOPs for wastewater treatment.

A green and economic approach to synthesize magnetic Lagenaria siceraria biochar (γ-Fe2O3-LSB) for methylene blue removal from aqueous solution.

In the printing and textile industries, methylene blue (a cationic azo dye) is commonly used. MB is a well-known carcinogen, and another major issue is its high content in industrial discharge. There are numerous removal methodologies that have been employed to remove it from industrial discharge; however, these current modalities have one or more limitations. In this research, a novel magnetized biochar (γ-Fe2O3-LSB) was synthesized using Lagenaria siceraria peels which were further magnetized via the co-precipitation method. The synthesized γ-Fe2O3-LSB was characterized using FTIR, X-ray diffraction, Raman, SEM-EDX, BET, and vibrating sample magnetometry (VSM) for the analysis of magnetic properties. γ-Fe2O3-LSB showed a reversible type IV isotherm, which is a primary characteristic of mesoporous materials. γ-Fe2O3-LSB had a specific surface area (SBET = 135.30 m2/g) which is greater than that of LSB (SBET = 11.54 m2/g). γ-Fe2O3-LSB exhibits a saturation magnetization value (Ms) of 3.72emu/g which shows its superparamagnetic nature. The batch adsorption process was performed to analyze the adsorptive removal of MB dye using γ-Fe2O3-LSB. The adsorption efficiency of γ-Fe2O3-LSB for MB was analyzed by varying parameters like the initial concentration of adsorbate (MB), γ-Fe2O3-LSB dose, pH effect, contact time, and temperature. Adsorption isotherm, kinetic, and thermodynamics were also studied after optimizing the protocol. The non-linear Langmuir model fitted the best to explain the adsorption isotherm mechanism and resulting adsorption capacity ( =54.55mg/g). The thermodynamics study showed the spontaneous and endothermic nature, and pseudo-second-order rate kinetics was followed during the adsorption process. Regeneration study showed that γ-Fe2O3-LSB can be used up to four cycles. In laboratory setup, the cost of γ-Fe2O3-LSB synthesis comes out to be 162.75 INR/kg which is low as compared to commercially available adsorbents. The results obtained suggest that magnetic Lagenaria siceraria biochar, which is economical and efficient, can be used as a potential biochar material for industrial applications in the treatment of wastewater.

Unlocking the potential of magnetic biochar in wastewater purification: a review on the removal of bisphenol A from aqueous solution.

Bisphenol A (BPA) is an essential and extensively utilized chemical compound with significant environmental and public health risks. This review critically assesses the current water purification techniques for BPA removal, emphasizing the efficacy of adsorption technology. Within this context, we probe into the synthesis of magnetic biochar (MBC) using co-precipitation, hydrothermal carbonization, mechanical ball milling, and impregnation pyrolysis as widely applied techniques. Our analysis scrutinizes the strengths and drawbacks of these techniques, with pyrolytic temperature emerging as a critical variable influencing the physicochemical properties and performance of MBC. We explored various modification techniques including oxidation, acid and alkaline modifications, element doping, surface functional modification, nanomaterial loading, and biological alteration, to overcome the drawbacks of pristine MBC, which typically exhibits reduced adsorption performance due to its magnetic medium. These modifications enhance the physicochemical properties of MBC, enabling it to efficiently adsorb contaminants from water. MBC is efficient in the removal of BPA from water. Magnetite and maghemite iron oxides are commonly used in MBC production, with MBC demonstrating effective BPA removal fitting well with Freundlich and Langmuir models. Notably, the pseudo-second-order model accurately describes BPA removal kinetics. Key adsorption mechanisms include pore filling, electrostatic attraction, hydrophobic interactions, hydrogen bonding, π-π interactions, and electron transfer surface interactions. This review provides valuable insights into BPA removal from water using MBC and suggests future research directions for real-world water purification applications.

The dual-configured hydrogen bonds induced by polymerized deep eutectic solvents-modified magnetic biochar enhanced the selectivity for 3,4-methylenedioxymethamphetamine

The accurate discovering and monitoring of 3,4-methylenedioxymethamphetamine (MDMA) are especially important because of its substantial toxicity and potential harm to human and the ecological systems. Three types of polymerized deep eutectic solvents functionalized magnetic biochar (MBC@poly (AA/AAC/AAm-ChCl)) were successfully synthesized to adsorb MDMA. The isotherm and kinetic data confirmed that MBC@poly (AAm-ChCl) had the strongest adsorption capacity, and the order of adsorption capacity is as follow: MBC@poly(AAm-ChCl) > MBC@poly(AA-ChCl) > MBC@poly(MAA-ChCl), which also revealed that the adsorption was heterogeneous multi-layer chemisorption. The findings of the characterizations manifested that MBC@poly(AAm-ChCl) was the optimal adsorbent owning to its higher nitrogen content, resulting in the formation of a greater number of hydrogen bonds. Due to the strong hydrogen bonding effect of CO and –NH2 functional groups, MBC@poly(AAm-ChCl) exhibited the high selectivity towards MDMA under the coexistence of multiple chemical substances, and excellent adsorption performance over the pH range of 4–11. Urea as a hydrogen bond inhibitor further confirmed MBC@poly(AAm-ChCl) had high-density active hydrogen bonding sites. Furthermore, utilizing density functional theory (DFT) for simulating adsorption both before and after the process verified that the high selectivity of MBC@poly(AAm-ChCl) attributed to the formation of the dual-configured hydrogen bonds. This study provides support for the production of highly selective biochar for use in pretreatment during drug detection.

Application of Hydroxyapatite Functionalized Magnetic Rice Husk Biochar for the Adsorption Removal of Cu(II) Ions from Aqueous Solutions

Application of Hydroxyapatite Functionalized Magnetic Rice Husk Biochar for the Adsorption Removal of Cu(II) Ions from Aqueous Solutions

Magnetic biochar catalyst from reed straw and electric furnace dust for biodiesel production and life cycle assessment

A novel magnetic carbon-based catalyst was prepared from solid waste (reed straw and electric furnace dust) by coprecipitation and high temperature pyrolysis with excellent application potential. Single factor and response surface experiments were used to optimize the catalyst preparation process (mass ratio of reed straw/electric furnace dust of 5:1 at 500 °C in 4 h) and biodiesel production, respectively, with results of 99.89 wt% biodiesel yield in the first cycle (93.61 wt% after 11 cycles) obtained at 74.15 °C in 4.16 h with a 14.06:1 M ratio of methanol/oil and 7.75 wt% catalyst. The life cycle assessment of magnetic carbon-based catalysts for biodiesel production suggested that the soybean oil extraction stage had the greatest impact on the environment, mainly from the use of soybeans and electricity. Solid waste as raw material to prepare catalysts for biomass energy conversion was proven to be a good strategy for energy conservation and emission reduction. This study provides guidance sustainable biomass energy conversion with low cost, low energy consumption, and minimal negative environmental impact.

Effective removal of microplastics by filamentous algae and its magnetic biochar: Performance and mechanism

In recent years, filamentous algae blooms and microplastics (MPs) pollution have become two major ecological and environmental problems in urban water systems. In order to solve these two problems at the same time, this study explored the loading capacity of MPs on fresh filamentous algae, and successfully synthesized magnetic filamentous algae biochar loading with Fe3O4 by hydrothermal method, with the purpose of removing MPs from water. The magnetic filamentous algal biochar was characterized by scanning electron microscopy (SEM), Fourier transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and so on. Experiments on adsorption kinetics, adsorption isotherms and optimum pH were carried out to explore the adsorption mechanism of MPs on magnetic filamentous algal biochar. The adsorption kinetics and adsorption isotherm models were evaluated, and the selection criterion for the appropriate model was determined by using the residual sum of squares (RSS) and Bayesian information criterion (BIC). Microscope images revealed that fresh filamentous algae could interact with MPs in the form of entanglement, adhesion and encapsulation. The average load of MPs in filamentous algae samples was 14.1 ± 5 items/g dry weight. The theoretical maximum adsorption capacities of polystyrene MPs (PS-MPs) by raw biochar (A500) and magnetic biochar with Fe3O4 (M2A500) were 176.99 mg/g and 215.58 mg/g, respectively. The adsorbent materials gave better reusability because they could be reused up to five times. Overall, these findings have provided new insights into the use of filamentous algae for in situ remediation of fluvial MPs pollution, as well as feasible strategies for the recycling of algal waste.

Enhanced degradation of atrazine from soil with recyclable magnetic carbon-based bacterial pellets: Performance and mechanism

Herein, magnetic biochar coupled with Acinetobacter lwoffii DNS32 immobilized pellets (DMBC-P) were synthesized through sodium alginate embedding and fixation, which could fast and completely eliminate atrazine from contaminated farmland soil. Characterization results revealed that DMBC-P exhibited a significant abundance of three-dimensional network porous structures, thereby enhancing the stability and specific surface area of DMBC-P. The application of 0.5 % DMBC-P could completely remove 22 mg/kg atrazine from soil within 4 d under the condition of moisture content of 60 % and soil pH of 7.4. After 5 d of remediation, DMBC-P could be easily extracted from the soil by magnetic separation and still had 100 % removal efficiency for atrazine after 3 rounds of recycling. Moreover, DMBC-P effectively alleviated the oxidative damage of atrazine to soybean seedlings through significantly decreasing the activities of various plants antioxidant enzymes by 27 % to 79 %. Meanwhile, analysis of 16S rRNA revealed a significant increase in the relative abundance of functional microflora such as Acidobacteriota and Chloroflexi at the phylum level, which promoted the growth of soybean seedlings. Additionally, pore filling, hydrogen bonding, and π-π stacking were identified as the primary mechanisms responsible for atrazine adsorption onto DMBC-P. Subsequently, the degrading bacteria DNS32 immobilized on DMBC-P was employed to catalyze the decomposition of atrazine into non-toxic cyanuric acid based on LC-MS. Overall, this study provided a reasonable design of magnetic carbon-based bacterial pellet for atrazine-contaminated soil remediation, which could efficiently remove atrazine and be effectively recycled after remediation.