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Stormwater pollution is a key factor contributing to water quality degradation, posing substantial environmental and human health risks. Although stormwater retention ponds, also referred to as wet ponds, are commonly implemented to alleviate stormwater challenges by reducing peak flow and removing suspended solids, their effectiveness in removing heavy metals and nutrients is limited. This study evaluated the performance of floating treatment platforms (FTPs) featuring vetiver grass (Chrysopogon zizanioides), a non-invasive, nutrient- and metal-accumulating perennial grass, in removing heavy metals (Cu, Pb, and Zn) and nutrients (P and N) in stormwater retention ponds. Furthermore, the potential for utilizing the spent vetiver biomass for generating biochar and bioethanol was investigated. The study was conducted in a greenhouse setup under simulated wet and dry weather conditions using pond water collected from a retention pond in Stafford Township, New Jersey, USA. Two FTPs with vetiver (vegetated FTPs) were compared with two FTPs without vetiver (non-vegetated FTPs), which served as controls. Results showed that the removal of heavy metals and nutrients by the FTPs with vetiver was significantly higher (p < 0.05) than the FTPs without vetiver. Notably, vetiver showed resilience to stormwater pollutants and hydroponic conditions, displaying no visible stress symptoms. The biochar and bioethanol generated from the spent vetiver exhibited desirable yield and quality, without raising concerns regarding pollutant leaching, indicated by very low TCLP and SPLP concentrations. This study provides compelling evidence that the implementation of vetiver-based FTPs offers a cost-effective and environment-friendly solution for mitigating stormwater pollution in retention ponds. Furthermore, the utilization of vetiver biomass for biofuel and biochar production supports clean production and fostering circular economy efforts. [Display omitted] • Vetiver-based floating treatment platform (FTP) was designed to retrofit wet ponds. • Vetiver-based FTP significantly enhanced the removal of nutrients and metals. • Vetiver was resilient to stormwater pollutants and hydroponic conditions. • Biochar and bioethanol produced from spent vetiver had desirable yield and quality. [ABSTRACT FROM AUTHOR]

Recent research has found biochar to be a cost-effective adsorbent for removal of perfluoroalkyl substances in water. To promote cleaner production and sustainable waste management, this study explored the potential to produce activated biochars by co-pyrolyzing sawdust with iron-rich biosolids and polyaluminum sludge. The maximum capacity to adsorb perfluorooctanesulfonic acid (PFOS) reached 27.2 mg g−1 with biosolids-activated biochar and 19.2 mg g−1 with aluminum sludge-activated biochar, compared to 6.2 mg g−1 with sawdust biochar. The increased adsorption capacities were attributed to electrostatic interactions between the anionic PFOS and metal functionalities on the biochar surface. In contrast, hydrophobic interaction was the dominant adsorption mechanism of sawdust biochar. The presence of dissolved organic matter at 5–50 mg L−1 was found to inhibit adsorption of PFOS in water, while pH as low as 3.0 and sodium chloride concentrations up to 100 mM enhanced removal of PFOS by all the three adsorbents. In batch adsorption tests at environmentally relevant PFOS dosages and adsorbent dosage of 0.25 g L−1, the biosolids-sawdust biochar and Al sludge-sawdust biochar removed 71.4% and 66.9% of PFOS from drinking water and 77.9% and 87.9% of PFOS from filtrate of sludge digestate, respectively. The biosolids-sawdust biochar additionally removed Fe, although the Al sludge-sawdust biochar released Al into the alkaline drinking water and filtrate. Overall, this study proved co-pyrolyzing sawdust and Fe-rich biosolids to be an effective approach to activate sawdust biochar for enhanced removal of PFOS while recycling wastewater treatment residuals and sawdust. [Display omitted] [ABSTRACT FROM AUTHOR]

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 Fe 3 O 4 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 Fe 3 O 4 (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. [Display omitted] • Removal effects of filamentous algae on MPs are investigated for the first time. • Growing filamentous algae can accumulate microplastics. • Biochar prepared from filamentous algal waste can effectively remove MPs. • Eco-friendly remediation approach is promising in reducing MP pollution. [ABSTRACT FROM AUTHOR]

Phosphorus (P) and Ammonium Nitrogen (N) are essential nutrients for plants and environmental stability. However, their excess in water causes eutrophication, damaging aquatic ecosystems. While adsorption is a promising solution, finding affordable and efficient adsorbents remains a challenge. In this study, magnesium (Mg), iron (Fe), and Mg/Fe doped biochars (BC) adsorbents were synthesized, and evaluated for adsorption of individual P and N and a P + N mixture from a solution and wastewater from a wastewater treatment plant. Compared to other adsorbents, Mg/BC showed excellent performance in adsorbing phosphorus (P) and ammonium nitrogen (N) from aqueous solutions. It demonstrated a large adsorption capacity of 64.65 mg/g and 62.50 mg/g from individual P and N solutions, and 30.3 mg/g and 27.67 mg/g from the P and N mixture solution, respectively. In addition, Mg/BC efficiently removed P and N from real-life wastewater. In the real wastewater, P and N removal efficiencies reached 88.30% and 59.36%, respectively. Kinetics analysis revealed that the pseudo-second-order model accurately described the adsorption of phosphorus (P) and ammonium nitrogen (N) in all solutions. The adsorbent followed the monolayer-Langmuir isotherm for N ions and the multilayer-Freundlich isotherm for P, indicating efficient adsorption processes. Thermodynamic experiments indicated that the adsorption of P and N was not only feasible but also occurred spontaneously in a natural manner. This study revealed that the strategic modification of biochar plays a crucial role in advancing effective wastewater treatment technologies designed for nutrient removal. [Display omitted] • Air calcined metal chloride adsorbents were devolved for P & N adsorption from wastewater. • Maximum adsorption P (64.65 mg/g) & N (62.50 mg/g) was found with Mg/BC adsorbent. • Efficiently simultaneous adsorption of P & N was achieved by Mg/BC adsorbent. • P and N adsorption mechanisms were studied. [ABSTRACT FROM AUTHOR]

Biochar has emerged as an efficacious green material for remediation of a wide spectrum of environmental pollutants. Biochar has excellent characteristics and can be used to reduce the bioavailability and leachability of emerging pollutants in soil through adsorption and other physico-chemical reactions. This paper systematically reviewed previous researches on application of biochar/engineered biochar for removal of soil contaminants, and underlying adsorption mechanism. Engineered biochar are derivatives of pristine biochar that are modified by various physico-chemical and biological procedures to improve their adsorption capacities for contaminants. This review will promote the possibility to expand the application of biochar for restoration of degraded lands in the industrial area or saline soil, and further increase the useable area. This review shows that application of biochar is a win-win strategy for recycling and utilization of waste biomass and environmental remediation. Application of biochar for remediation of contaminated soils may provide a new solution to the problem of soil pollution. However, these studies were performed mainly in a laboratory or a small scale, hence, further investigations are required to fill the research gaps and to check real-time applicability of engineered biochar on the industrial contaminated sites for its large-scale application. [Display omitted] • Biochar application is a promising strategy for remediation of contaminated soil. • Removal of emerging contaminants from soil by biochar is explicated emphatically. • Challenges and future prospects of restoring degraded soil by biochar have been illustrated. [ABSTRACT FROM AUTHOR]

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. [Display omitted] • Methods of preparing biochar adsorbents for PFAS adsorption were summarized. • Mechanisms of PFAS adsorption on biochar adsorbents were comprehensively explored. • The effectiveness of biochar for PFAS removal is closely tied to pyrolysis conditions. • Activated biochars exhibited enhanced PFAS adsorption performance compared to pristine biochars. • Biochar Composites showed higher PFAS adsorption performance. [ABSTRACT FROM AUTHOR]

In the face of increasing nitrogen demand for crop cultivation driven by population growth, this study presents a sustainable solution to address both the heightened demand and the energy-intensive process of nitrogen removal from wastewater. Our approach involves the removal of nitrogen from wastewater and its subsequent return to the soil as a fertilizer. Using biochar derived from Aesculus turbinata fruit shells (ATFS), a by-product of post-medical use, we investigated the effect of pyrolysis temperature on the NH 4 –N adsorption capacity of ATFS biochar (ATFS-BC). Notably, the ATFS-BC pyrolyzed at 300 °C (ATFS-BC300) exhibited the highest NH 4 –N adsorption capacity of 15.61 mg/g. The superior performance of ATFS-BC300 was attributed to its higher number of oxygen functional groups and more negatively charged surface, which contributed to the enhanced NH 4 –N adsorption. The removal of NH 4 –N by ATFS-BC300 involved both physical diffusion and chemisorption, with NH 4 –N forming a robust multilayer adsorption on the biochar. Alkaline conditions favored NH 4 –N adsorption by ATFS-BC300; however, the presence of trivalent and divalent ions hindered this process. Rice plants were cultivated to assess the potential of NH 4 –N adsorbed ATFS-BC300 (NH 4 -ATFS-BC300) as a nitrogen fertilizer. Remarkably, medium doses of NH 4 -ATFS-BC300 (594.5 kg/ha) exhibited key agronomic traits similar to those of the commercial nitrogen fertilizer in rice seedlings. Furthermore, high doses of NH 4 -ATFS-BC300 demonstrated superior agronomic traits compared to the commercial fertilizer. This study establishes the viability of utilizing ATFS-BC300 as a dual-purpose solution for wastewater treatment and nitrogen fertilizer supply, presenting a promising avenue for addressing environmental challenges. [Display omitted] • Biochar from Aesculus turbinata fruit shells (ATFS) is a valuable resource. • ATFS was used as an adsorbent for NH 4 –N removal in wastewater. • ATFS pyrolyzed at 300 °C showed the highest NH 4 –N adsorption. • The NH 4 –N adsorbed ATFS-BC was a beneficial nitrogen fertilizer for rice growth. [ABSTRACT FROM AUTHOR]

In this comprehensive study, highlights emerging environmentally friendly methods to eliminating hazardous heavy metals from contaminated water, with an emphasis on bioremediation and biosorption. Breakthroughs, such as the combination of biological remediation and nanotechnology to improve the elimination of metals effectiveness and the use of genetically modified microbes for targeted pollutant breakdown. Developing biosorption materials made from agricultural waste and biochar, this indicates interesting areas for future research and emphasizes the necessity of sustainable practices in tackling heavy metal contamination in water systems. There seems to be a surge in enthusiasm for the utilization of biological remediation and biosorption methods as sustainable and viable options for eliminating heavy metals from contaminated water in the past couple of decades. The present review intends to offer an in-depth review of the latest understanding and advances in the discipline of biological remediation methods like bioaccumulation, biofiltration, bio-slurping, and bio-venting. Biosorption is specifically explained and includes waste biomass as biosorbent with the removal mechanisms and the hindrances caused in the process are detailed. Advances in biosorption like microbes as biosorbents and the mechanism involved in it. Additionally, novel enhancement techniques like immobilization, genetic modification, and ultrasound-assisted treatment in microbial sorbent are clarified. However, the review extended with analyzing the future advances in the overall biological methods and consequences of heavy metal pollution. [Display omitted] • Biological techniques for the effective removal of heavy metal ions were discussed. • Various biosorbents sources, mechanism and influencing parameters were summarized. • Microbes surface qualities are modified using genetic modifications are reviewed. • Future and advanced views on biological adsorption techniques were elucidated. [ABSTRACT FROM AUTHOR]

The non-free radical oxidation pathway (PMS-NOPs) of peroxymonosulfate (PMS) holds significant promise for practical wastewater treatment applications, owing to its low oxidation potential, high PMS utilization rate, and robust anti-interference capability in the degradation of pollutants. A novel activator copper nitrogen co-doped porous biochar (Cu-N-BC) with rich defect edges and functional groups was obtained by adding Cu and N to the biochar matrix generated by sodium alginate through pyrolysis in this study. Under the condition of 1 mM PMS, 30 mg/L activator was used to activate PMS and achieve efficient degradation of 10 mg/L paracetamol (PCT) within 15 min, with a high reaction rate constants (k obs) of 0.391 min−1. The activation mechanism of the Cu-N-BC/PMS/PCT system was a non-radical activation pathway with the dominance of singlet oxygen (1O 2) and the presence of catalyst-mediated electron transfer. The graphite nitrogen, pyridine nitrogen, and Cu–N coordination introduced by Cu/N co-doping, as well as the carbon skeleton and C O functional group of biochar, were considered active sites that promote the 1O 2 generation. The Cu-N-BC/PMS system exhibits strong stability, eco-friendliness, effective mineralization, and interference resistance across diverse pH levels (3–11) and interfering ions, including Cl−, H 2 PO 4 −, NO 3 −, SO 4 2−, and humic acid. Remarkably, it efficiently degrades PCT in tap and lake water, achieving a notable 63.73% TOC mineralization rate, with leached copper ions below 0.02 mg/L. This research introduces a novel method for obtaining metal nitrogen carbon activators and enhances understanding of PMS non-radical activation pathways and active sites. [Display omitted] • A strategy of co-doping biochar was developed to construct a non-radical activation mechanism of PMS. • The degradation efficiency of paracetamol can reach 100% with low-dose activators. • Singlet oxygen and electron transfer were responsible for the degradation. [ABSTRACT FROM AUTHOR]

Carbon-based biowaste incorporated with inorganic oxides as a composite is an enticing option to mitigate heavy metal pollution in water resources due to its more economical and efficient performance. With this in mind, we constructed manganese-doped iron oxide microflowers resembling the dandelion-like structure on the surface of cold plasma-treated carbonized rice husk (MnFe 2 O 3 /PCRH). The prepared composite exhibited 45% and 19% higher removal rates for Cu2+ and Cd2+, respectively than the pristine CRH. The MnFe 2 O 3 /PCRH composite was characterized using XRD, FTIR, FESEM, EDX, HR-TEM, XPS, BET, TGA, and zeta potential, while the adsorption capacities were investigated as a function of pH, time, and initial concentration in batch trials. As for the kinetics, the pseudo-second-order was the rate-limiting over the pseudo-first-order and Elovich model, demonstrating that the chemisorption process governed the adsorption of Cu2+ and Cd2+. Additionally, the maximum adsorption capacities of the MnFe 2 O 3 /PCRH were found to be 122.8 and 102.5 mg/g for Cu2+ and Cd2+, respectively. Based on thorough examinations by FESEM-EDS, FTIR, and XPS, the possible mechanisms for the adsorption can be ascribed to surface complexation by oxygen-containing groups, a dissolution-precipitation of the ions with –OH groups, electrostatic attraction between metal ions and the adsorbent's partially charged surface, coordination of Cu2+ and Cd2+ with π electrons by aromatic/graphitic carbon in the MnFe 2 O 3 /PCRH, and pore filling and diffusion. Lastly, the adsorption efficiencies were maintained at about 70% of its initial adsorption even after five adsorption-desorption cycles, displaying its remarkable stability and reusability. [Display omitted] • Mn-doped Fe 2 O 3 microflowers were decorated on plasma-treated biochar (MnFe 2 O 3 /PCRH). • The MnFe 2 O 3 /PCRH was thoroughly analyzed before and after Cu2+ and Cd2+ adsorption. • Kinetics, isotherms, and thermodynamic studies showed its excellent adsorption capability. • Mechanisms underlying ions adsorption by MnFe 2 O 3 /PCRH were further clarified. • The reusability of the MnFe2O3/PCRH proved its economic sustainability. [ABSTRACT FROM AUTHOR]

In recent times, the application of biochar (BC) as an upcoming catalyst for the elimination of recalcitrant pollutants has been widely explored. Here, an iron loaded bamboo biochar activated peroxymonosulphate (PMS) process was tested for removing Congo red (CR) dye from water medium. The catalyst was synthesized using a green synthesis method using neem extracts and characterized using SEM, FTIR, and XRD. The effects of various operating parameters, including solution pH, catalyst dosage, and pollutant dosage, on dye degradation efficiency were examined. The results showed that at the optimized conditions of 300 mg L−1 PMS concentration, 200 mg L−1 catalyst dosage, and pH 6, about 89.7% of CR dye (initial concentration 10 ppm) was removed at 60 min of operation. Scavenging experiments revealed the significant contribution of O 2 •−, •OH, and 1O 2 for dye degradation, with a major contribution of O 2 •−. The activation of PMS was mainly done by biochar rather than iron (loaded on biochar). The catalyst was highly active even after four cycles. [Display omitted] • Application of green synthesized iron-loaded biochar as a PMS activator. • The superior performance of biochar in the activation by PMS. • O 2.•− is the primary oxidant responsible for dye degradation • •OH and 1O 2 were also produced in the catalyst-activated PMS process • SO 4.•− has less contribution to dye degradation [ABSTRACT FROM AUTHOR]

The presence of heavy metals in water pose a serious threat to both public and environmental health. However, the advances in the application of low cost biochar based adsorbent synthesize from various feedstocks plays an effective role in the of removal heavy metals from water. This study implies the introduction of novel method of converting food waste (FW) to biochar through pyrolysis, examine its physiochemical characteristics, and investigate its adsorption potential for the removal of heavy metals from water. The results revealed that biochar yield decreased from 18.4 % to 14.31 % with increase in pyrolysis temperature from 350 to 550 °C. Likewise, increase in the pyrolysis temperature also resulted in the increase in the ash content from 39.87 % to 42.05 % thus transforming the biochar into alkaline nature (pH 10.17). The structural and chemical compositions of biochar produced at various temperatures (350, 450, and 550 °C) showed a wide range of mineralogical composition, and changes in the concentration of surface functional groups. Similarly, the adsorption potential showed that all the produced biochar effectively removed the selected heavy metals from wastewater. However a slightly high removal capacity was observed for biochar produced at 550 °C that was credited to the alkaline nature, negatively charged biochar active sites due to O-containing functional groups and swelling behavior. The results also showed that the maximum adsorption was recorded at pH 8 at adsorbent dose of 2.5 g L−1 with the contact time of 120 min. To express the adsorption equilibrium, the results were subjected to Langmuir and Freundlich isotherms and correlation coefficient implies that the adsorption process follows the Freundlich adsorption isotherm. The findings of this study suggest the suitability of the novel FW derived biochar as an effective and low cost adsorbent for the removal of heavy metals form wastewater. [Display omitted] • Biochar was successfully produced from food waste at various pyrolysis temperatures. • Temperatures significantly affect the physiochemical characteristics of biochar. • Biochar showed effective adsorption capacity towards the removal of heavy metals. • pH 8, 2.5 g L−1 adsorbent dose and 120 min contact time showed high adsorption. • Adsorption equilibrium fitted best with Freundlich adsorption isotherm model. [ABSTRACT FROM AUTHOR]

An important paradigm shift towards the circular economy is to prioritize waste prevention, reuse, recycling, and recovery before disposal is necessary. In this context, a sustainable protocol of converting waste pea peel (wPP) into low-cost carbon nanomaterials for sensing and conversion of p -nitrophenol (p -NP) into value-added paracetamol is being reported. Two fractions of the carbonaceous nanomaterials were obtained after the hydrothermal treatment (HT) of wPP, firstly an aqueous portion containing water-soluble carbon dots (wPP-CDs) and a solid residue, which was converted into carbonized biochar (wPP-BC). Blue-colored fluorescent wPP-CDs displayed excitation-dependent and pH-independent properties with a quantum yield (QY) of 8.82 %, which were exploited for the fluorescence sensing of p -NP with 4.20 μM limit of detection. Pyrolyzed biochar acting as an efficient catalyst effectively reduces p -NP to p -aminophenol (p -AP) in just 16 min with a 0.237 min−1 rate of conversion. Furthermore, the produced p -AP was converted into paracetamol, an analgesic and antipyretic drug, to achieve zero waste theory. Thus, this study provides the execution of sustainable approaches based on the integral valorization of biowaste that can be further recycled and reused, offering an effective way to attain a profitable circular economy. [Display omitted] • Value-added carbon nanomaterials were synthesized from waste pea peels. • Blue fluorescent carbon dots act as a fluorescent sensor for p -nitrophenol (p -NP). • Solid biochar serves as a promising catalyst for the efficient reduction of p -NP. • The obtained p -aminophenol was further converted into a valuable drug, paracetamol. [ABSTRACT FROM AUTHOR]

Acacia Senegal waste (ASW) is remaining biomass following gum Arabic harvesting and has no use mentioned in the literature as of yet. This study aims to convert ASW into valuable biochar via two comparative thermal and hydrothermal techniques, which include pyrochar ASW at 300 °C (PC ASW300) and hydrochar ASW at 180 °C (HC ASW180), respectively, for Cu (II) adsorption from aqueous solutions. SEM-EDS, FTIR, XRD, and XPS were used to characterize the biochar. Adsorption performance was studied as a function of pH, contact time, and adsorbent concentration. Adsorption kinetics were best fit for a pseudo-second-order model. And thermodynamics studies revealed that Cu (II) on biochar was endothermic, spontaneous, and best fitted to the Langmuir isotherm model. Pyrochar adsorption capacity (31.93 mg g−1) was seven times that of hydrochar (5.45 mg g−1). ASW treated with phosphorus (PC H 3 PO 4 and HC H 3 PO 4) prior to the carbonization altered the pore structure and surface functional groups as well (O–P–O, P–CH 3 , and P–OH) of biochar. It was found that treating with phosphorous acid increased adsorption capacity to 141.7 mg g−1 and 22.24 mg g−1 for PC H 3 PO 4 and HC H 3 PO 4 , respectively. The surface functional groups of biochar resulted from lignin, alkaloids, and polysaccharides combined with Cu (II) during the adsorption process via surface complexation accompanied by π-electron interaction and Cu (II) reduction. These findings shed light on the ASW biochar potential as a new green cost-effective adsorbent and drew an insightful understanding of Cu (II) adsorption performance and mechanism. It is concluded that ASW-derived biochar is highly effective and a promising alternative for Cu (II) decontamination from wastewater. [Display omitted] • Acacia Senegal waste biochar has a potential as Cu(II) cost-effective adsorbents. • Phosphorous activated biochar grew Cu(II) adsorption capacity up to five times. • Copper adsorption on surface of biochar was accompanied by Cu(II) reduction. • Surface complexation and π electron interaction played a key role on adsorption. • Pyrochar show greater adsorption capacity and removal efficiency than hydrochar. [ABSTRACT FROM AUTHOR]

This study investigated the catalytic activity of biochar materials derived from algal biomass Sargassum fusiforme (S. fusiforme) for groundwater remediation. A facile single-step pyrolysis process was used to prepare S. fusiforme biochar (SFBC X), where x denotes pyrolysis temperatures (600 °C-900 °C). The surface characterization revealed that SFBC 800 possesses intrinsic N and P heteroatoms. The optimum experimental condition for acetaminophen (AAP) degradation (>98.70%) was achieved in 60 min using 1.0 mM peroxymonosulfate (PMS), 100 mg L−1 SFBC 800 , and pH 5.8 (unadjusted). Moreover, the degradation rate constant (k) was evaluated by the pseudo-first-order kinetic model. The maximum degradation (>98.70%) of AAP was achieved within 60 min of oxidation. Subsequently, the k value was calculated to be 6.7 × 10−2 min−1. The scavenger tests showed that radical and nonradical processes are involved in the SFBC 800 /PMS system. Moreover, the formation of reactive oxygen species (ROS) in the SFBC 800 /PMS system was confirmed using electron spin resonance (ESR) spectroscopy. Intriguingly, both radical (O 2 •−, •OH, and SO 4 •−) and nonradical (1O 2) ROS were formed in the SFBC 800 /PMS system. In addition, electrochemical studies were conducted to verify the electron transfer process of the nonradical mechanism in the SFBC 800 /PMS system. The scavenger and electron spin resonance (ESR) spectroscopy showed that singlet oxygen (1O 2) is the predominant component in AAP degradation. Under optimal condition, the SFBC 800 /PMS system reached ∼81% mineralization of AAP within 5 min and continued to ∼85% achieved over 60 min of oxidation. Coexisting ions and different aqueous matrices were investigated to examine the feasibility of the catalyst system, and the SFBC 800 /PMS system was found to be effective in the remediation of AAP-contaminated groundwater, river water, and effluent water obtained from wastewater treatment plants. Moreover, the SFBC 800 -activated PMS system demonstrated reusability. Our findings indicate that the SFBC 800 catalyst has excellent catalytic activity for AAP degradation in aquatic environments. [Display omitted] • PMS-activated Sargassum fusiforme biochar (SFBC 800) boosts acetaminophen breakdown. • Inherent N and P in SFBC 800 enhance the AAP degradation pathway. • Singlet oxygen (1O 2) is the dominant component in the SFBC 800 /PMS system. • SFBC 800 demonstrated reusability in groundwater, surface water, and wastewater. [ABSTRACT FROM AUTHOR]

The co-transport behavior of environmental pollutants with biochar particles has aroused great interests from researchers due to the concerns about pollutant diffusion and environmental exposure after biochar is applied to soil. In this work, the recovery and co-transport behavior of biochar micron-/nano-particles (BCMP and BCNP) and lead (Pb2+) in saturated porous media were investigated under different ionic strength conditions (IS = 1, 5 and 10 mM) under a direct current electric field. The results showed that the electric field could significantly enhance the mobility of Pb adsorbed biochar particles, particularly BCNP. The recovery of Pb laden biochar particles was improved by 1.8 folds, reaching 78.8% at maximum under favorable condition at +0.5 V cm−1. According to the CDE (Convection-Dispersion-Equation) model and DLVO (Derjaguin-Landau-Verwey-Overbeek) theory analysis, the electric field facilitated the transport of Pb carried biochar mainly by increasing the negative charges on biochar surface and improving the repulsive force between biochar and porous media. High IS was favorable for biochar transport under the electric field, but inhibited desorbing Pb2+ from biochar (18% by maximum at IS = 10 mM). By switching the electric field power, a two-stage strategy was established to maximize the recovery of both biochar particles and Pb, where BCNP and Pb recovery were higher than electric field free case by 90% and 35%, respectively. The findings of this study can help build a biochar recovery approach to prevent potential risks from biochar application in heavy metal contaminated soil remediation. [Display omitted] • Electric field promoted the migration of both Pb laden/free biochar particles. • Up to 78.8% of Pb2+ laden biochar nano-particles recovered under 0.5 V·cm-1. • Electric field detach about 18% adsorbed Pb from biochar under high ionic strength. • Two-stage strategy were proposed to recover both biochar and Pb2+. [ABSTRACT FROM AUTHOR]

Biochar-based materials for air treatment have gained significant attention for removing health-detrimental volatile organic compounds (VOCs) and particulate matter (PM) in indoor air settings. However, high turnaround time, multiple pretreatment processes involved, and high pore size and low surface area (>10 μm, <100 m2 g−1) of lignocellulosic feedstocks demand alternative biochar feedstock material. Considering this, we designed a simple first-of-its-kind indoor air scrubbing material using diatoms-enriched microalgae biochar. In the present study, the microalgae were cultivated on waste anaerobic digestate (biogas slurry) and were pyrolyzed at three different temperatures: 300 °C (BC300), 500 °C (BC500), and 700 °C (BC700). The BC500 and BC700 showed the highest removal efficiencies (99 %) for total volatile organic carbons (TVOCs) and formaldehyde (HCHO) at concentrations of 1.22 mg m−3 HCHO and 8.57 mg m−3 TVOC compared to 50% efficiency obtained with commercially available surgical, cloth, and N95 masks. The biochar obtained showed a high Brunauer–Emmett–Teller (BET) surface area of 238 m2 g−1 (BC500) and 480 m2 g−1 (BC700) and an average pore size of 9–11 nm due to the mesoporous characteristic of diatom frustules. The comparatively poor performance of BC300 was due to lower surface area (150 m2 g−1) arising from incomplete organic removal, as evidenced by FESEM-EDX and FTIR. The high removal efficiencies in BC500 and BC700 were also attributed to the presence of reactive functional groups such as –OH and R–NH 2. Concurrently, the average particulate matter (PM10, PM2.5, and PM1) removal efficiency for BC500 and BC 700 ranged between 66 and 82.69 %. The PM removal performance of BC500 and BC700 was lower (15–20%) than commercially available masks. Overall, the present study highlights the importance of diatoms (reactive Si) present inside the pores of microalgal biochar for enhanced removal of PM, TVOCs, and HCHO at temperatures above 500 °C. This complete approach signifies a step towards establishing a self-sustainable and circular process characterized by minimal waste generation for indoor air treatment. [Display omitted] • Simultaneous removal of particulate matter PM10, PM2.5, PM1, TVOC's and HCHO. • Microalgal biochar contained 21.2 %w/w silica diatoms with pore size of 9–11 nm. • Diatoms increased specific surface area 2X (482 m2 g−1) than conventional biochars. • Developed material highly specific in removal of TVOC's and HCHO (∼99%). [ABSTRACT FROM AUTHOR]

Soil salinization is a major environmental hazard that limits land availability. Human-induced salt pollutants (HISPs) are regularly presented in large quantities on the contaminated site (such as brine leakages and salt-water spills), causing a devastating shock with high salt stress to the ecosystem. For instance, Saskatchewan resulted in a 48% drop in wheat production and a 0.3% decline in provincial GDP. As the calcium-modified biochar can potentially ameliorate the negative effects of HISPs on plants and improve the plant, phytoremediation with calcium-modified biochar can have increased detoxification of hazardous pollutants from sites. Therefore, the objective of our study was to develop a biochar-assisted phytoremediation employing diverse approaches to calcium modification for the sustainable removal of HISPs. The co-pyrolyzed calcium biochar achieved a remarkable removal rate of 18.06%, reducing salinity from 9.44 to 7.81 dS/m. During a 90-day long-term phytoremediation, the overall reduction rate of calcium-modified biochar stimulated the germination and growth of Thinopyrum ponticum. The result of post-treatment further indicated that co-pyrolyzed biochar with Ca transferred salt into the plant compared to Ca-coated biochar, which only immobilized HISPs on its surface. These results offer two different treatment approaches for diverse situations involving HISPs contamination, addressing current in-situ spills and providing a calcium-related biochar technology for further research in desalination. [Display omitted] • Ca-coated and Ca-copyrolyzed biochar for phytoremediation of saline soil were investigated. • Ca-modified biochars generated from copyrolysis and coating. • Ca-modified biochars displayed enhanced capability in direct removing salt from brine water • In a 90-day phytoremediation, Ca-modified biochar reduced salinity and improved soil quality • Ca-copyrolyzed and Ca-coated biochar have diverse roles in salt migration into vegetations [ABSTRACT FROM AUTHOR]

Polycyclic aromatic hydrocarbons (PAHs) are pervasive ecological pollutants produced essentially during the inadequate burning of organic materials. PAHs are a group of different organic compounds that are made out of various aromatic rings. PAHs pose a serious risk to humans and aquatic ecosystems because of their mutagenic and carcinogenic properties. In this way, there is a critical prerequisite to utilizing successful remediation strategies and methods to limit the dangerous effect of these pollutants on the ecosystem. Biochar has believed of intriguing properties such as simple manufacturing operations and more affordable and more productive materials. Biochar is a sustainable carbonaceous material that has an enormous surface area with bountiful functional groups and pore structure, which has huge potential for the remediation of toxic pollutants. This review emphasizes the occurrence, development, and fate of toxic PAHs in the environment. In the present review, the properties and role of biochar in the removal of PAHs were illustrated, and the influencing factors and an efficient key mechanism of biochar for the remediation of PAHs were discussed in detail. Various surface modification methods can be utilized to improve the biochar properties with the magnetization process; the advancements of modified biochar are pointed out in this review. Finally, the constraints and prospects for the large-scale application of biochar in the remediation of toxic pollutants are highlighted. [Display omitted] • Utilization of biochar as an effective strategy for PAH remediation has been reviewed. • Overview on Surface and functional properties of biochar used for PAH removal was emphasized. • Role and primary mechanisms of different biochar in PAH removal has been detailed in the review. • Modification for enhancement of biochar properties for effective removal of PAH was described. [ABSTRACT FROM AUTHOR]

The fertosphere, as the interfaces between fertilizer granular and soil particles, represents a key hotspot for nitrogen transformation processes, particularly for ammonia (NH 3) and nitrous oxide (N 2 O) emissions. Understanding the heterogeneity of the fertosphere, especially when incorporating organic amendments like biochars, is crucial for predicting NH 3 and N 2 O emissions after soil fertilization. In this study, we investigated the effects of three types of biochar (pristine, aged, and acid-washed biochar) on heterogeneity of fertosphere induced by localized urea application. pH-specific planar optodes were employed to visualize pH gradients in fertosphere hotspots with high spatial and temporal resolution. In addition, we conducted thorough measurements of the gradient distribution of electric conductivity (EC), mineral N, aqueous NH 3 in soil and enzyme activities relevant to nitrification. Concurrently, NH 3 and N 2 O emissions from the soil were continuously monitored at a high temporal resolution. Initially, urea-induced fertosphere exhibited significant NH 3 emissions, primarily attributed to the pH elevation resulting from urea hydrolysis. However, after 6 days, NH 3 emissions subsided, and there was a notable sharp increase in N 2 O emissions. Importantly, compared to urea application alone, the inclusion of pristine biochar led to a delay in soil pH decline with a 19% rise in NH 3 emission. Aged biochar, characterized by a higher content of oxygen functional groups, demonstrated increased NH 4 +/NH 3 adsorption capacity and enhanced ammonia monooxygenase (AMO) activity in soil, resulting in an 18% reduction in NH 3 emission. While a slight decrease of 5% in NH 3 cumulative emission was observed in the acid-washed biochar treatment. Notably, biochar could potentially promote nitrification-derived N 2 O emissions due to the accumulation of NH 3 oxidation products (NH 2 OH). These findings could contribute to refining N transformation models for fertilized soils, and optimizing N fertilizer application strategies. [Display omitted] • Localized urea application induced pH gradients along fertosphere up to 25 mm. • TAN and NO 3 −-N had opposite gradients across the fertosphere. • Biochar could attenuate the heterogeneity of fertosphere, but promote NH 3 emissions. • Increased AMO and decreased HAO nitrification enzyme activities raised N 2 O emission. [ABSTRACT FROM AUTHOR]

Activated carbon (AC) has important industrial and environmental applications as it has excellent abilities to sorb contaminants such as per- and polyfluoroalkyl substances (PFAS). Current research aims to develop activated biochars (AB) from renewable biomass to replace AC that is produced from fossil feedstock. Both AC and AB are primarily comprised of condensed aromatic carbon (ConAC), the component that is the focus of this study. ConAC is characterized to determine its relationship with biochar activation conditions and PFAS sorption, which are understudied at present. Benzenepolycarboxylic acid (BPCA) markers for ConAC were quantified in steam-activated biochars (AB-Steam) and carbon dioxide-activated biochars (AB-CO 2) prepared from waste timber at different temperatures (800, 850, 900 °C) and molar ratios of feedstock-carbon:steam (0.50 – 1.25). A non-activated biochar was also included as a reference. ConAC relative to total organic carbon content was higher in AB-Steam than in AB-CO 2 (92 ± 2 % vs. 81 ± 11%). The ratio of benzenehexa- (B6CA) to benzenepentacarboxylic (B5CA) acids revealed that AB-Steam also had larger ConAC clusters than AB-CO 2. These findings provide novel evidence that steam activation is more effective than CO 2 activation in creating ConAC. To assess how ConAC impacts AB sorption abilities, AB-Steam were used to remediate PFAS from contaminated soils. The observed strong correlations between ConAC content and sorption of long-chain PFAS suggest the importance of hydrophobic interactions between PFAS tails and ConAC. Poor correlations for short-chain PFAS, on the other hand, indicated the existence of electrostatic repulsion interactions between PFAS head groups and ConAC. Collectively, these results explain the great ability of AB-Steam to sorb PFAS from contaminated soils (up to 100% remediation). More broadly, this work demonstrates that the BPCA method can be a valuable tool to assess the quality of biochars and other carbonaceous sorbents in relation to their production conditions or contaminant sorption abilities. [Display omitted] • Condensed aromatic carbon (ConAC) content was determined by benzenepolycarboxylic acid (BPCA) markers. • Steam-activated biochars had more ConAC (92 ± 2 %) of larger cluster size than CO 2 -activated biochars (81 ± 11%). • More PFAS sorption (71 ± 25%) was observed at higher ConAC content (> 92%). • Hydrophobic and electrostatic repulsion interactions likely exist between PFAS and ConAC. [ABSTRACT FROM AUTHOR]

The application of carbon nanoparticles (CNPs) and biochar in agriculture for improving plant health and soil quality and alleviating metal stress offers alternative approaches to meet the ever-increasing demand for food. However, poor understanding of their roles in improving crop production under Cu stress represents a significant obstacle to their wide application in agriculture. To clarify how CNPs and biochar affect corn (Zea mays L.) seed germination, seedling growth, plant health, and nutrient uptake under different Cu stress levels, soil-less Petri-dish and greenhouse soil-based bioassays were conducted. The results revealed that CNPs and biochar stimulated corn seed germination and seedling growth. Besides, they were effective in immobilizing Cu2+ sorption in sandy soil and alleviating Cu stress for plant growth, as shown by the increased plant height and dry biomass. The plant nutrient uptake efficiency (NUE) was significantly increased by CNPs, with a maximum increase of 63.1% for N and 63.3% for K at the highest Cu2+ stress level (400 mg Cu2+ L−1). In contrast, non-significant effects on NUE were observed with biochar treatments regardless of Cu stress levels. Interestingly, CNPs significantly increased plant uptake of Cu in the Petri dish test, while biochar inhibited plant uptake of Cu under both experimental conditions. Principle component analysis (PCA) and Pearson correlation analysis indicated that CNPs mitigated Cu stress mainly by elevating antioxidant enzyme activities, enhancing plant photochemical efficiency, and increasing plant uptake of N and K, while biochar was more likely to reduce bioavailability and uptake of Cu in the plant. These findings have great implications for the application of CNPs and biochar as plant growth stimulators and de-toxicity agents in agriculture. [Display omitted] • CNPs and biochar improved seed germination and plant growth under Cu stress. • CNPs elevated antioxidant enzyme activities, enhanced plant photochemical efficiency and plant uptake of N and K. • Biochar reduced Cu concentration and decreased activities of antioxidant enzymes in plants. [ABSTRACT FROM AUTHOR]

This study evaluates pyrolysis products obtained from biomasses (silver grass, pine, and acacia) harvested from heavy-metal-contaminated soil. To do so, we utilized two methods: a batch one-stage pyrolysis, and a continuous two-stage pyrolysis. The study results show that the yields and characteristics of bio-oils and biochars varied depending on the pyrolysis process and the type of biomass. The two-stage pyrolysis having two reactors (auger and fluidized bed reactors) appeared to be very suitable for specific chemicals production such as acetic acid, acetol, catechol, and levoglucosan. The biochar obtained from the fluidized-bed reactor of two-stage pyrolysis had high thermal stability, high crystallinity, high inorganic content, and a small number of functional groups. In contrast, the biochar obtained from the one-stage pyrolysis had low thermal stability, low crystallinity, a high carbon content, and a large number of functional groups. The biochar obtained from the two-stage pyrolysis appeared to be suitable as a material for catalyst support and as an adsorbent. The biochar obtained from one-stage pyrolysis appeared to be a suitable as a soil amendment, as an adsorbent, and as a precursor of activated carbon. All biochars showed a negative carbon footprint. In the end, this study, which was conducted using two different processes, was able to obtain the fact that products of pyrolysis biomass contaminated with heavy metals have different characteristics depending on the process characteristics and that their utilization plans are different accordingly. If the optimal utilization method proposed through this study is found, pyrolysis will be able to gain importance as an effective treatment method for biomass contaminated with heavy metals. [Display omitted] • Results of one-stage and two-stage pyrolysis of contaminated biomass were compared. • Two-stage pyrolysis turned out to be suitable for specific chemicals production. • Biochar from fluidized-bed reactor has potential as catalyst support and absorbent. • Biochar from fixed-bed reactor has potential as soil amendment and absorbent. • All biochars seemed to be applicable in construction field as sustainable materials. [ABSTRACT FROM AUTHOR]

In this study, a novel Fe 3 O 4 -based biochar coupled surface-imprinted polymer was constructed via simple hydrothermal route for salicylic acid recognition and degradation in advanced oxidation processes. The material exhibited excellent adsorption capability, up to 118.23 mg g−1, and efficient degradation performance, 87.44% removal rate within 240 min, based on integrating the advantages of both huge specific surface area as well as abundant functional groups from biochars and specific recognition sites from imprinted cavities. Moreover, high selectivity coefficient (11.67) showed stable recognition in single and binary systems. SO 4 •− and •OH were confirmed as reactive oxygen species in catalytic reaction according to quenching experiments and EPR analysis. The degradation mechanism and pathway were unraveled by DFT calculations and LC-MS. Furthermore, the results of toxicity evaluation, stability and reusability demonstrated application potential in the field of water environment restoration. This study confirmed that molecular imprinting provided a promising solution to targeted removal of emerging environmental pollutants by degrading after the enrichment of pollutants to the composites surface. [Display omitted] • A novel molecularly imprinted polymers coated Fe 3 O 4 -BC was successfully synthesized. • Adsorption-degradation activities and specific recognition of SA by MI-FBC were improved. • MI-FBC exhibited good stability and regenerability with tolerance to wide pH and anions. • The mechanism and pathway of SA removal were proposed based on experiments and DFT calculations. [ABSTRACT FROM AUTHOR]

Removal of toxic dyes such as Rhodamine B is essential as it pollutes aqueous and soil streams as well. This comprehensive study explores the potential of Calophyllum inophyllum seed char as an efficient bio-adsorbent based on their characteristic properties and a comparative study between various carbon-based adsorbents on the adsorption capacity of Rhodamine B dye. In this study, the char was prepared from Calophyllum inophyllum seed using a slow pyrolysis process (298 K/min) at an optimum temperature of 823 K and used as an adsorbent for the removal of Rhodamine B from water. The resulting char was mesoporous and had 155.389 m2/g surface areas (BET) and 0.628 cc/g pore volume. The formation of pores was observed from the SEM analysis. The adsorption studies were tested and optimized through various parameters such as solution pH, adsorbent dosage, initial dye concentration, stirring speed, contact time, and solution temperature. Maximum 95.5 % removal of Rhodamine B was possible at the pH: 2, stirring speed: 100 rpm, time: 25 min, temperature 308 K, and dose: 1.2 g/L. The highest adsorption capacity at equilibrium was determined to be 169.5 (mg/g) through Langmuir adsorption isotherm studies and followed pseudo 2nd order kinetics. The thermodynamics study confirmed the adsorption processes were spontaneous (ΔG°=−0.735 kJ/mol) and endothermic (ΔH° = 4.1 kJ/mol) processes. The reusability study confirmed that the mesoporous char can be reused as an efficient adsorbent for up to 3 cycles for environmental remediation. [Display omitted] • Non-edible seed pyrolytic char is a good adsorbent for the removal of dye. • Seed char is a mesoporous and nano structured adsorbent. • Dye adsorption was high in acidic medium. • Possible to remove 95 % Rhodamine B dye at 1.2 g/L adsorbent dosage. • The biochar can be used up to three cycles and can be regenerated. [ABSTRACT FROM AUTHOR]

Cadmium (Cd) is classified as a heavy metal (HM) and is found into the environment through both natural processes and intensified anthropogenic activities such as industrial operations, mining, disposal of metal-laden waste like batteries, as well as sludge disposal, excessive fertilizer application, and Cd-related product usage. This rising Cd disposal into the environment carries substantial risks to the food chain and human well-being. Inadequate regulatory measures have led to Cd bio-accumulation in plants, which is increasing in an alarming rate and further jeopardizing higher trophic organisms, including humans. In response, an effective Cd decontamination strategy such as phytoremediation emerges as a potent solution, with innovations in nanotechnology like biochar (BC) and nanoparticles (NPs) further augmenting its effectiveness for Cd phytoremediation. BC, derived from biomass pyrolysis, and a variety of NPs, both natural and less toxic, actively engage in Cd removal during phytoremediation, mitigating plant toxicity and associated hazards. This review scrutinizes the application of BC and NPs in Cd phytoremediation, assessing their synergistic mechanism in influencing plant growth, genetic regulations, structural transformations, and phytohormone dynamics. Additionally, the review also underscores the adoption of this sustainable and environmentally friendly strategies for future research in employing BC-NP microaggregates to ameliorate Cd phytoremediation from soil, thereby curbing ecological damage due to Cd toxicity. [Display omitted] • Cd toxicity varies with factors such as metal form, pH, and exposure duration. • Address protocols, impacts, economics, and toxicity in Cd phytoremediation. • Phytoremediation economically mitigates HM pollution, preserving ecosystems. • BC enhances nutrient availability, microbial communities, and Cd adsorption. • BC and NPs synergistically reduce Cd toxicity, improving soil and plant health. [ABSTRACT FROM AUTHOR]

Production of medium-chain fatty acids (MCFAs) from sewage sludge has dual effects on valuable sludge disposal and renewable energy generation, while low efficiency limits its application. Biochar addition is considered an effective method to improve MCFAs production. In this study, the influence of biochar adding strategies (i.e., adding biochar in acidification or chain elongation (CE) processes) on MCFAs production was explored. Results showed that by adding biochar in the acidification process, MCFAs accumulation increased by over 114%, accompanied by the highest carbon conversion efficiency (134.66%) and electron transfer efficiency of MCFAs (94.22%) by the terminal CE. Adding biochar before the acidification process better enriched CE bacteria (e.g., Paraclostridium) and strengthened the dominant metabolic pathway. In contrast, the biochar added before the CE process priorly enriched the bacteria capable of degrading organics, like unclassified_f__Dysgonomonadaceae , norank_f__norank_o__OPB41 , and Acetobacterium. The differences in excessive ethanol oxidation and short-chain fatty acids accumulation induced by varied adding strategies might be responsible for this. [Display omitted] • Adding strategy influenced the bacteria and metabolic pathways in MCFA production. • Adding biochar in the acidification process benefited MCFAs accumulation. • Adding biochar in the CE process better enriched the acidification bacteria. • Microbial analysis clarified the key genus varied with different adding strategies. [ABSTRACT FROM AUTHOR]

Robust membrane modifiers were achieved for the first time by functionalizing the algal biochar of unique porous structure. The biochar was prepared through the pyrolysis of Cladophora glomerata , the most widespread freshwater macroalga, functionalized by diethylenetriamine and dendrimer poly(amidoamine), and employed to fabricate positively charged composite nanofiltration membranes. The presence of hydrophilic functionalizers of positive charge on the membrane was verified through Fourier transform infrared and energy dispersive X-ray analyses and atomic force microscopy and zeta potential measurements were performed to determine surface roughness and confirm positive charge of the modified membranes. Dispersion of modifiers on the surface and morphology of the were also revealed through field-emission scanning electron microscopy images. It has shown that, compared to the pristine membrane, pure water fluxes were increased by 214% and 185%, and water contact angles were reduced from 66.1° to 39.5° and 43.3° in those modified by biochar functionalized with dendrimer poly(amidoamine) and diethylenetriamine, respectively. More than 90% dye rejections and salt and heavy metals removals were recorded for the membranes possessed 0.6 wt% of modifiers. Finally, a comparative study conducted between the novel modifier introduced in this study and those reported in the literature, indicated that C. glomerata biochar decorated with amine functional groups could be considered as a robust and practical alternative to the common modifiers used to manipulate nanocomposite membranes characteristics. [Display omitted] • Novel modifier introduced from the most widespread macroalga of environmental issue. • C. glomerata biochar is functionalized with amine groups to possess positive charge. • Introduced biochar can be a robust alternative to typical membrane modifiers. • Flux and filtration performance improved in positively charged modified membranes. • Advanced heavy metal rejection achieved by incorporation of functionalized modifier. [ABSTRACT FROM AUTHOR]

Cr(VI) contamination is widely recognized as one of the major environmental hazards. To address the problem of remediation of soil Cr(VI) contamination and utilization of waste peanut shells, this study comprehensively investigated the effects of peanut shell-derived biochar loaded with root exudates of hyperaccumulator Leersia hexandra Swartz on Cr(VI) reduction and microbial community succession in soil. This study confirmed that root exudate-loaded peanut shell biochar reduced soil pH while simultaneously increasing DOC, sulfide, and Fe(II) concentrations, thereby facilitating the reduction of Cr(VI), achieving a reduction efficiency of 81.8%. Based on XPS and SEM elemental mapping analyses, Cr(VI) reduction occurred concurrently with the Fe and S redox cycles. Furthermore, the microbial diversity, abundance of the functional genera (Geobacter , Arthrobacter , and Desulfococcus) and the metabolic functions associated with Cr(VI) reduction were enhanced by root exudate-loaded biochar. Root exudate-loaded biochar can promote both direct Cr(VI) reduction mediated by the Cr(VI)-reducing bacteria Arthrobacter , and indirect Cr(VI) reduction through Cr/S/Fe co-transformation mediated by the sulfate-reducing bacteria Desulfococcus and Fe(III)-reducing bacteria Geobacter. This study demonstrates the effectiveness of peanut shell biochar loaded with root exudates of hyperaccumulator Leersia hexandra Swartz to promote soil Cr(VI) reduction, reveals the mechanism how root exudate-loaded biochar shapes functional microbial communities to facilitate Cr(VI) reduction, and proposes a viable strategy for Cr(VI) remediation and utilization of peanut shell. [Display omitted] • Peanut shell biochar loaded with root exudates of L. hexandra facilitated Cr(VI) reduction. • Root exudate-loaded biochar enhanced Cr(VI) reduction by shaping microbial communities. • Cr(VI) reduction occurred concurrently with Fe and S redox cycles. • Root exudate-loaded biochar promoted indirect Cr(VI) reduction through Cr/S/Fe co-transformation. • Geobacter , Arthrobacter , and Desulfococcus are involved in Cr(VI) reduction. [ABSTRACT FROM AUTHOR]

Thermo-chemical behavior of a microalgal biomass; Dunaliella salina was investigated through thermo-gravimetric analyses. Fully-grown D. salina biomass were subjected for biochar conversion using pyrolytic treatment at three distinct heating rates such as 2.5, 5, and 15 °C min−1. The kinetic appraisals were explained by using model-free kinetics viz., Kissinger-Akahira-Sanose, Flynn-Waal-Ozawa and Starink iso-conversional correlations with concomitant evaluation of activation energies (E a). The Ea value is 194.2 kJ mol−1 at 90% conversion in FWO model, which is higher as compared to other two models. Moisture, volatile substances, and other biochemical components of the biomass were volatilized between 400 and 1000 K in two separate thermo-chemical breakdown regimes. Microscopic and surface characterization analyses were carried out to elucidate the elemental and morphological characteristics of the biomass and biochar. Further, the proficiency of the prepared biochar was tested for removing naphthalene from the watery media. The novelty of the present study lies in extending the applicability of biochar prepared from D. salina for the removal of a model polyaromatic hydrocarbon, naphthalene. [Display omitted] • Prepared microalgal biochar exhibited superior naphthalene sorption from aqueous media. • Utilized Freundlich isotherm and pseudo-second order kinetics to elucidate sorption. • D. salina -derived biochar's surface complexation facilitated naphthalene sorption. • Prepared biochar combines microalgal biomass valorization with pollution reduction. [ABSTRACT FROM AUTHOR]

As a cost-effective material, biochar, known as 'black gold', has been widely used for environmental applications (EA), including chromium-contaminated wastewater remediation. However, limited reports focused on the multiple impacts of biochar, including energy consumption (EC) and environmental risk (ER). Hence, to recommend biochar as a green material for sustainable development, the three critical units were explored and quantitatively assessed based on an adapted 3E model (EA-EC-ER). The tested biochar was produced by limited-oxygen pyrolysis at 400–700 °C by using three typical biomasses (Ulva prolifera , phoenix tree, and municipal sludge), and the optimal operational modulus of the 3E model was identified using six key indicators. The findings revealed a significant positive correlation between EC and biochar yield (p < 0.05). The biochar produced by phoenix tree consumed more energy due to having higher content of unstable carbon fractions. Further, high-temperature and low-temperature biochar demonstrated different chromium removal mechanisms. Notably, the biochar produced at low temperature (400 °C) achieved better EA due to having high removal capacity and stability. Regarding ER, pyrolysis temperature of 500 °C could effectively stabilize the ecological risk in all biochar and the biochar produced by Ulva prolifera depicted the greatest reduction (37-fold). However, the increase in pyrolysis temperature would lead to an increase in global warming potential by nearly 22 times. Finally, the 3E model disclosed that the biochar produced by Ulva prolifera at 500 °C with low EC, high EA, and low ER had the most positive recommendation index (+78%). Importantly, a rapid assessment methodology was established by extracting parameters from the correlation. Based on this methodology, about eight percent of biochar can be the highest recommended from more than 100 collected peer-related data. Overall, the obtained findings highlighted that the multiple impacts of biochar should be considered to efficiently advance global sustainable development goals. [Display omitted] • An adapted 3E model assessed three critical units of typical biochar. • Yield is a key factor in the energy consumption of biochar. • Biochar produced at low temperatures has a greater Cr removal performance. • Ulva prolifera biochar has the maximum recommendation index. • A rapid assessment methodology was established by extracting parameters. [ABSTRACT FROM AUTHOR]

The growing global population has led to a heightened need for food production, and this rise in agricultural activity is closely tied to the application of phosphorus-based fertilizers, which contributes to the depletion of rock phosphate (RP) reserves. Considering the limited P reserves, different approaches were conducted previously for P removal from waste streams, while the adsorption of ions is a novel strategy with more applicability. In this study, a comprehensive method was employed to recover phosphorus from wastewater by utilizing biochar engineered with minerals such as calcium, magnesium, and iron. Elemental analysis of the wastewater following a batch experiment indicated the efficiency of the engineered biochar as an adsorbent. Subsequently, the phosphorus-enriched biochar, hereinafter (PL-BCsb), obtained from the wastewater, underwent further analysis through FTIR, XRD, and nutritional assessments. The results revealed that the PL-BCsb contained four times higher (1.82%) P contents which further reused as a fertilizer supplementation for Brassica napus L growth. PL-BCsb showed citric acid (34.03%), Olsen solution (10.99%), and water soluble (1.74%) P desorption. Additionally, phosphorous solubilizing bacteria (PSB) were incorporated with PL-BCsb along two P fertilizer levels P45 (45 kg ha−1) and P90 (90 kg ha−1) for evaluation of phosphorus reuse efficiency. Integrated application of PL-BCsb with half of the suggested amount of P45 (45 kg ha−1) and PSB increased growth, production, physiological, biochemical, and nutritional qualities of canola by almost two folds when compared to control. Similarly, it also improved soil microbial biomass carbon up to four times, alkaline and acid phosphatases activities both by one and half times respectively as compared to control P (0). Furthermore, this investigation demonstrated that waste-to-fertilizer technology enhanced the phosphorus fertilizer use efficiency by 55–60% while reducing phosphorus losses into water streams by 90%. These results have significant implications for reducing eutrophication, making it a promising approach for mitigating environmental pollution and addressing climate change. [Display omitted] • Sugarcane bagasse biochar was produced and engineered with Ca, Mg and Fe. • Phosphorus (P) adsorption was performed from eutrophic wastewater. • P laden biochar (PL-BCsb) harvested by P precipitation with Ca+2, Mg+2, and Fe+3. • P adsorption was accomplished and confirmed by FTIR and XRD analyses. • PL-BCsb was evaluated as fertilizer to canola growth and development in pot study. [ABSTRACT FROM AUTHOR]

For environmental sustainability and to achieve sustainable development goals (SDGs), drinking water treatment must be done at a reasonable cost with minimal environmental impact. Therefore, treating contaminated drinking water requires materials and approaches that are inexpensive, produced locally, and effortlessly. Hence, locally available materials and their derivatives, such as biochar (BC) and activated carbon (AC) were investigated thoroughly. Several researchers and their findings show that the application of locally accessible materials and their derivatives are capable of the adsorptive removal of organic and inorganic contaminants from drinking water. The application of locally available materials such as lignocellulosic materials/waste and its thermo-chemically derived products, including BC and AC were found effective in the treatment of contaminated drinking water. Thus, this review aims to thoroughly examine the latest developments in the use of locally accessible feedstocks for tailoring BC and AC, as well as their features and applications in the treatment of drinking water. We attempted to explain facts related to the potential mechanisms of BC and AC, such as complexation, co-precipitation, electrostatic interaction, and ion exchange to treat water, thereby achieving a risk-free remediation approach to polluted water. Additionally, this research offers guidance on creating efficient household treatment units based on the health risks associated with customized adsorbents and cost-benefit analyses. Lastly, this review work discusses the current obstacles for using locally accessible materials and their thermo-chemically produced by-products to purify drinking water, as well as the necessity for technological interventions. [Display omitted] • Local materials and its derivatives in treatment of water has been discussed. • Properties of BC and AC derived from locally available materials were elaborated. • Mechanism in removal of organic and inorganic pollutants were discussed. • Development of BC and AC based household treatment units were deliberated. • Economy of BC and AC based water treatment units were elaborated. [ABSTRACT FROM AUTHOR]

The UV/sulfite-based advanced reduction process (ARP) emerges as an effective strategy to combat per- and polyfluoroalkyl substances (PFAS) pollution in water. Yet, the UV/sulfite-ARP typically operates at highly alkaline conditions (e.g., pH > 9 or even higher) since the generated reductive radicals for PFAS degradation can be quickly sequestered by protons (H+). To overcome the associated challenges, we prototyped a biochar-surfactant-system (BSS) to synergistically enhance PFAS sorption and degradation by UV/sulfite-ARP. The degradation and defluorination efficiencies of perfluorooctanoic acid (PFOA) depended on solution pH, and concentrations of surfactant (cetyltrimethylammonium bromide; CTAB), sulfite, and biochar. At high pH (8–10), adding biochar and BSS showed no or even small inhibitory effect on PFOA degradation, since the degradation efficiencies were already high enough that cannot be differentiated. However, at acidic and neutral pH (6–7), an evident enhancement of PFOA degradation and defluorination efficiencies occurred. This is due to the synergies between biochar and CTAB that create favorable microenvironments for enhanced PFOA sorption and deeper destruction by prolonging the longevity of reductive radicals (e.g., SO 3 •−), which is less affected by ambient pH conditions. The performance of UV/sulfite/BSS was further optimized and used for the degradation of four PFAS. At the optimal experimental condition, the UV/sulfite/BSS system can completely degrade PFOA with >30% defluorination efficiency for up to five continuous cycles (n = 5). Overall, our BSS provides a cost-effective and sustainable technique to effectively degrade PFAS in water under environmentally relevant pH conditions. The BSS-enabled ARP technique can be easily tied into PFAS treatment train technology (e.g., advanced oxidation process) for more efficient and deeper defluorination of various PFAS in water. [Display omitted] • Biochar-surfactant-system (BSS) was prototyped for PFAS sorption and destruction. • BSS enhanced sorption and destruction of various PFAS at neutral pH. • Efficient defluorination of PFOA was achieved for five continuous cycles. • BSS-enabled advanced reduction process is promising for PFAS remediation. [ABSTRACT FROM AUTHOR]

Groundwater pollution caused by the leakage of petroleum and various fuel oils is becoming a serious environmental problem. In this study, carbon-based materials including biochar and hydrochar were applied to investigate the effects of additives on the toluene removal in the extracted groundwater under microaerobic condition with the addition of nitrate. Biochar and hydrochar could adsorb toluene, and thus enhance the toluene removal in the system. The toluene removal efficiency was 8.2–8.9 mg/(g·h) at the beginning, and then decreased with time in the control and the hydrochar treatment, while it remained the stable values in the biochar treatment, owing to the fact that biochar could reduce the NO 3 −-N loss by partial denitrification. Moreover, biochar could prompt the growth of toluene-degrading bacteria including Thauera , Rhodococcus, Ideonella and Denitratisoma, which had the capability of denitrification. However, hydrochar could stimulated the growth of denitrifiers without toluene-degrading capacity including Candidatus Competibacter and Ferrovibrio , which might play a key role in the partial denitrification of the system. The findings are helpful for developing remediation techniques of contaminated groundwater. [Display omitted] • Biochar and hydrochar can adsorb toluene and enhance toluene removal. • Biochar can reduce the NO 3 −-N loss by the partial denitrification. • Biochar can prompt the growth of toluene-degrading bacteria. • Low NO 3 −-N concentrations can reduce toluene-degrading capacity. [ABSTRACT FROM AUTHOR]

The intensive accumulation of di-2-ethylhexyl phthalate (DEHP) in agricultural soils has resulted in severe environmental pollution that endangers ecosystem and human health. Biochar is an eco-friendly material that can help in accelerating organic pollutant degradation; nevertheless, its roles in enhancing DEHP removal in rhizosphere remain unclear. This work investigated the impacts of biochar dosage (0%–2.0%) on DEHP degradation performance in tomato rhizosphere by comprehensively exploring the change in DEHP metabolites, bacterial communities and DEHP-degrading genes. Our results showed a significant increase of rhizosphere pH, organic matter and humus by biochar amendment, which achieved a satisfactorily higher DEHP removal efficiency, maximally 77.53% in treatments with 1.0% of biochar. Biochar addition also remarkably changed rhizosphere bacterial communities by enriching some potential DEHP degraders of Nocardioides , Sphingomonas , Bradyrhizobium and Rhodanobacter. The abundance of genes encoding key enzymes (hydrolase, esterase and cytochrome P450) and DEHP-degrading genes (pht3 , pht4 , pht5 , benC-xylZ and benD-xylL) were increased after biochar amendment, leading to the change in DEHP degradation metabolism, primarily from benzoic acid pathway to protocatechuic acid pathway. Our findings evidenced that biochar amendment could accelerate DEHP degradation by altering rhizosphere soil physicochemical variables, bacterial community composition and metabolic genes, providing clues for the mechanisms of biochar-assisted DEHP degradation in organic contaminated farmland soils. [Display omitted] • The accelerated DEHP degradation in the tomato rhizosphere amended with biochar can be explained by the higher pH and humus levels. • Biochar amendment changed DEHP degradation pathways from benzoic acid to protocatechuic acid. • More genes encoding DEHP-degrading enzymes in biochar treatments. [ABSTRACT FROM AUTHOR]

Nuclear energy is playing an increasingly important role on the earth, but the nuclear plants leaves a legacy of radioactive waste pollution, especially uranium-containing pollution. Straw biochar with wide sources, large output, low cost, and easy availability, has emerged as a promising material for uranium extraction from radioactive wastewater, but the natural biomass with suboptimal structure and low content of functional groups limits the efficiency. In this work, microbial etch was first came up to regulate the biochar's structure and function. The surface of the biochar becomes rougher and more microporous, and the mineral contents (Ca, P) indirectly increased by microbial etch. The biochar was modified by calcium phosphate and exhibited a remarkable uranium extraction capacity of 590.8 mg g−1 (fitted value). This work provides a cost-effective and sustainable method for preparing functionalized biochar via microbial etch, which has potential for application to uranium extraction from radioactive wastewater. [Display omitted] • Microbial etch process constructed a large amount of Ca sites in the cotton straw. • Microbial etch facilitated the formation of calcium phosphate on the hydrothermal biochar. • The adsorption capacity of CCS-P for U(VI) was 590.8 mg g−1. • Microbial etch is a novel method for the production of high-performance uranium adsorbent. [ABSTRACT FROM AUTHOR]

The widespread and inevitable use of plastic has led to prospective ecological problems through Bisphenol A (BPA), a synthetic chemical in plastic manufacturing. The present study addresses a unique methodology for eliminating BPA using the assistance of Pseudomonas putida. In the present work, biomass was torrefied to generate biochar with highly porous networks that could accommodate the bacterial species for effective colonization and multiplication. The designed biochar-bacterial globules demonstrated the ability to effectively remove BPA (96.88%) at a concentration of up to 2 g/L. The biochar-bacterial globules could effectively adsorb BPA at a low concentration of 20 mg/L. The alteration in pH did not impact the globule's performance, providing additional support for the practical utilization of these globules in polluted water bodies. In addition, the biochar-bacterial globules exhibited superior effectiveness in degradation compared to the standard levels, particularly in saline conditions. The simplicity and effectiveness of the approach make it promising for real-world implementation in addressing ecological problems associated with BPA contamination. [Display omitted] • The study addresses degradation and removal of Bisphenol A in natural water bodies. • Bacterial-biochar globules are sensitive to removal even upto 20 mg/L of BPA. • The fabricated globules are made for one-time use with easy disposal. • A possible mechanism for the enhanced degradation of BPA has been proposed. [ABSTRACT FROM AUTHOR]

CuCoFe-LDO/BCD was successfully synthesized from CuCoFe-LDH and biochar derived from durian shell (BCD). Ciprofloxacin (CFX) degraded more than 95% mainly by O 2 •− and 1O 2 in CuCoFe-LDO/BCD(2/1)/PMS system within 10 min with a rate constant of 0.255 min−1, which was 14.35 and 2.66 times higher than those in BCD/PMS and CuCoFe-LDO/PMS systems, respectively. The catalytic system exhibited good performance over a wide pH range (3–9) and high degradation efficiency of other antibiotics. Built-in electric field (BIEF) driven by large difference in the work function/Fermi level ratio between CuCoFe-LDO and BCD accelerated continuous electron transfer from CuCoFe-LDO to BCD to result in two different microenvironments with opposite charges at the interface, which enhanced PMS adsorption and activation via different directions. As a non-radical, 1O 2 was mainly generated via PMS activation by C=O in BCD. The presence of C=O in BCD resulted in an increase in atomic charge of C in C=O and redistributed the charge density of other C atoms. As a result, strong adsorption of PMS at C atom in C=O and other C with a high positive charge was favorable for 1O 2 generation, whereas an enhanced adsorption of PMS at negatively charged C accounted for the generation of •OH and SO 4 •−. After adsorption, electrons in C of BCD became deficient and were fulfilled with those transferred from CuCoFe-LDO driven by BIEF, which ensured the high catalytic activity of CuCoFe-LDO/BCD. O 2 •−, on the other hand, was generated via several pathways that involved in the transformation of •OH and SO 4 •− originated from PMS activation by the transition of metal species in CuCoFe-LDO and negatively charged C in BCD. This study proposed a new idea of fabricating a low-cost metal-LDH and biomass-derived catalyst with a strong synergistic effect induced by BIEF for enhancing PMS activation and antibiotic degradation. [Display omitted] • Durian peel-derived biochar enhances CFX degradation in CuCoFe-LDO/BCD/PMS by 1.48 times. • The role of C=O in BCD for PMS activation and 1O 2 generation is confirmed by DFT calculations. • A new pathway for 1O 2 generation via PMS activation by C=O is proposed. • Built-in electric field between CuCoFe-LDO and BCD accelerates electron transfer and enhances PMS activation. • CFX degradation is contributed mainly by both radical (O 2 •−) and non-radical (1O 2). [ABSTRACT FROM AUTHOR]

Oil sands process affected water (OSPW) is produced during bitumen extraction and typically contains high concentrations of trace metals. Constructed wetlands have emerged as a cost effective and green technology for the treatment of metals in wastewaters. Whether the addition of amendments to constructed wetlands can improve metal removal efficiency is unknown. We investigated the synergistic effects of carbon based amendments and wetland plant species in removal of arsenic, cadmium, cobalt, chromium, copper, nickel, and selenium from OSPW. Three native wetland species (Carex aquatilis , Juncus balticus , Scirpus validus) and two amendments (canola straw biochar, nano humus) were investigated in constructed wetland mesocosms over 60 days. Amendment effect on metal removal efficiency was not significant, while plant species effect was. Phytoremediation resulted in removal efficiencies of 78.61–96.31 % for arsenic, cadmium, and cobalt. Carex aquatilis had the highest removal efficiencies for all metals. Amendments alone performed well in removing some metals and were comparable to phytoremediation for cadmium, cobalt, copper, and nickel. Metals were primarily distributed in roots with negligible translocation to shoots. Our work provides insights into the role of plants and amendments during metal remediation and their complex interactions in constructed treatment wetlands. [Display omitted] • Carbon based amendments did not improve phytoremediation. • All native plant species efficiently removed arsenic, cadmium and cobalt from OSPW. • Carex aquatilis had highest removal efficiency for all seven metals. • Amendments alone were efficient for removal of cadmium, cobalt, copper, nickel. • Longer than 60 days is required to reduce metal concentrations to below guidelines. [ABSTRACT FROM AUTHOR]

The ecological risks of sewage sludge biochar (SSB) after land use is still not truly reflected. Herein, the ecological risks of SSB prepared at different temperature were investigated using the earthworm E. fetida as a model organism from the perspectives of organismal, tissue, cellular, and molecular level. The findings revealed that the ecological risk associated with low-temperature SSB (SSB 300) was more pronounced compared to medium- and high-temperature SSB (SSB 500 and SSB 700), and the ecological risk intensified with increasing SSB addition rates, as revealed by an increase in the integrated biomarker response v2 (IBRv2) value by 2.59–25.41 compared to those of SSB 500 and SSB 700. Among them, 10% SSB 300 application caused significant oxidative stress and neurotoxicity in earthworms compared to CK (p < 0.001). The weight growth rate and cocoon production rate of earthworms were observed to decrease by 25.06% and 69.29%, respectively, while the mortality rate exhibited a significant increase of 33.34% following a 10% SSB 300 application, as compared to the CK. Moreover, 10% SSB 300 application also resulted in extensive stratum corneum injury and significant longitudinal muscle damage in earthworms, while also inducing severe collapse of intestinal epithelial cells and disruption of intestinal integrity. In addition, 10% SSB 300 caused abnormal expression of earthworm detoxification and cocoon production genes (p < 0.001). These results may improve our understanding of the ecotoxicity of biochar, especially in the long term application, and contribute to providing the guidelines for applying biochar as a soil amendment. [Display omitted] • SSB 300 has stronger ecological risks than SSB 500 and SSB 700. • SSB disrupted antioxidant defense response and caused neurotoxicity. • SSB reduced earthworm biomass growth, survival, and reproduction. • SSB destroyed the lysosomal stability and caused histopathological lesions. • SSB regulated the abnormal mRNA expression of functionally-related genes. [ABSTRACT FROM AUTHOR]

The aim of the present study was to find environmentally friendly solutions for the disposal of problematic and toxic textile sludge (TS) by producing textile sludge biochar (TSB) by pyrolysis and evaluating its chemical properties, polycyclic aromatic hydrocarbon (PAH) content, heavy metals (HMs) speciation, environmental risks, and effects on seed germination. Pyrolysis of TS at temperatures ranging from 300 to 700 °C significantly reduced (85–95%) or eliminated certain PAHs in the biochar, enriched heavy metal content within land use limits, and increased bioavailability of HMs in biochar produced at 300 °C and decreased leaching capacity of HMs in biochar produced at 700 °C. The speciation of HMs and their bioavailability during pyrolysis processes was strongly temperature dependent, with lower temperatures increasing the toxic and bioavailable forms of Zn and Ni, while higher temperatures converted the bioavailable Ni to a more stable form, while Cu, Cr, and Pb were transformed from stable to toxic and bioavailable forms. The ecological risk index (RI) values of TSB-300 and TSB-700 are below the threshold value of 150, indicating a low-risk level, and the risk level decreases at temperatures above 500 °C. Further, the extracts of TSB-300 and TSB-700 had the highest percentage of germinating seeds, while the extracts of TS and TSB-500 inhibited seed germination by 20–30% compared to the control. These results indicate that pyrolysis effectively reduces PAHs and binds leachable HMs in biochar, however, the specific pyrolysis temperature influences metal speciation, bioavailability, seed germination, and environmental risk. [Display omitted] • Disposal of TS containing HMs poses a high environmental risk. • PAHs are reduced significantly by pyrolysis of TS into biochar. • Higher temperatures produce biochar with a stable form of Ni. • Environmental risk index of 700 °C biochar was the lowest. • Extracts of biochar produced at 700 °C promote plant growth. [ABSTRACT FROM AUTHOR]

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 FeCl 3 -treated peanut husk at different temperatures (300, 600, and 900 °C). Preliminary experiments demonstrated that MBC 600 exhibited superior performance, with its characterization confirming the presence of γ-Fe 2 O 3. 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 (MBC 600). [Display omitted] • PFOA adsorption from aqueous matrices by peanut husk-derived magnetic biochar studied. • Highest PFOA removal of 98.3% attained in 60 min at adsorbent dose: 400 mg/L, pH: 3.4. • Pseudo-second-order and Freundlich models better described PFOA adsorption process. • Electrostatic and hydrophobic interactions, and hydrogen bonding governed PFOA removal. • RSM-CCD, ANN, and ANFIS agreeably predicted adsorptive PFOA removal with R2 > 0.99. [ABSTRACT FROM AUTHOR]

Heavy metal contamination poses a significant threat to soil quality, plant growth, and food safety, and directly affects multiple UN SDGs. Addressing this issue and offering a remediation solution are vital for human health. One effective approach for immobilizing heavy metals involves impregnating cypress chips with calcium hydroxide (Ca(OH) 2) to enhance the chemical adsorption capacity of the resulting woody charcoal. In the present study, un-treated cypress biochar (UCBC) and calcium-treated cypress biochar (TCBC), were introduced into pristine and contaminated soil, at rates of 3, 6, and 9% (w/w). Both BCs were alkaline (UCBC pH: 8.9, TCBC pH: 9.7) with high specific surface area, which improved the soil properties (pH, EC, and OM). Radish (Raphanus sativus) cultivated in pots revealed that both UCBC and TCBC demonstrated significant improvements in growth attributes and heavy metal immobilization compared to the control, with TCBC exhibiting superior effects. The TCBC surface showed highly active nanosized precipitated calcium carbonate particles that were active in immobilizing heavy metals. The application of TCBC at a rate of 9% resulted in a substantial reduction in Zn and Cu uptake by radish roots and shoots. In contaminated soil, Zn uptake by radish roots decreased by 55% (68.3–31.0 mg kg−1), and shoots by 37% (49.3–31.0 mg kg−1); Cu uptake decreased by 40% (38.6–23.2 mg kg−1) in roots and 39% (58.2–35.2 mg kg−1) in shoots. Uptake of Pb was undetectable after TCBC application. Principal component analysis (PCA) highlighted the potential of TCBC over UCBC in reducing heavy metal concentrations and promoting radish growth. Future research should consider the long-term effects and microbial interactions of TCBC application. [Display omitted] • To immobilize Zn, Cu, and Pb in soil, a novel biochar (TCBC) was prepared. • TCBC improved soil properties and radish growth attributes. • TCBC resulted in a substantial reduction in Zn, Cu, and Pb in radish roots and shoots. • Highly active nano-sized CaCO 3 particles in TCBC-immobilized heavy metals. • TCBC consistently outperformed UCBC in terms of immobilization properties. [ABSTRACT FROM AUTHOR]

As an effort to tackle some of the most pressing ecological issues we are currently experiencing, there has been an increasing interest in employing biomass-derived char products in various disciplines. Thermal combustion of biomass results in biochar production, which is a remarkably rich source of carbon. Not only does the biochar obtained by the thermochemical breakdown of biomass lower the quantity of carbon released into the environment, but it also serves as an eco-friendly substitute for activated carbon (AC) and further carbon-containing products. An overview of using biochar to remove toxic pollutants is the main subject of this article. Several techniques for producing biochar have been explored. The most popular processes for producing biochar are hydrothermal carbonization, gasification and pyrolysis. Carbonaceous materials, alkali, acid and steam are all capable of altering biochar. Depending on the environmental domains of applications, several modification techniques are chosen. The current findings on characterization and potential applications of biochar are compiled in this survey. Comprehensive discussion is given on the fundamentals regarding the formation of biochar. Process variables influencing the yield of biochar have been summarized. Several biochars' adsorption capabilities for expulsion pollutants under various operating circumstances are compiled. In the domain of developing biochar, a few suggestions for future study have been given. [Display omitted] • This survey looked into the production of biochar using various techniques. • Process variables that affect the yield of biochar were emphasized. • This article briefly describes the biochar synthesis mechanism. • Biochar application for the evacuation of organic and inorganic pollutants was briefed. • Synthesis and application of magnetic biochar was summarized. [ABSTRACT FROM AUTHOR]

Soil salinization and sodication harm soil fertility and crop production, especially in dry regions. To combat this, using biochar combined with gypsum, lime, and farm manure is a promising solution for improving salt-affected soils. In a pot experiment, cotton stick biochar (BC) was applied at a rate of 20 t/ha in combination with gypsum (G), lime (L), and farm manure (F) at rates of 5 and 10 t/ha. These were denoted as BCG-5, BCL-5, BCF-5, BCG-10, BCL-10, and BCF-10. Three different types of soils with electrical conductivity (EC) to sodium adsorption ratio (SAR) ratios of 2.45:13.7, 9.45:22, and 11.56:40 were used for experimentation. The application of BCG-10 led to significant improvements in rice biomass, chlorophyll content, and overall growth. It was observed that applying BCG-10 to soils increased the membrane stability index by 75% in EC:SAR (2.45:13.7), 97% in EC:SAR (9.45:22), and 40% in EC:SAR (11.56:40) compared to respective control treatments. After BCG-10 was applied, the hydrogen peroxide in leaves dropped by 29%, 23%, and 21% in EC:SAR (2.45:13.7), EC:SAR (9.45:22), and EC:SAR (11.56:40) soils, relative to their controls, respectively. The application of BCG-10 resulted in glycine betaine increases of 60, 119, and 165% in EC: SAR (2.45:13.7), EC: SAR (9.45:22), and EC: SAR (11.56:40) soils. EC: SAR (2.45:13.7), EC: SAR (9.45:22), and EC: SAR (11.56:40) soils all had 70, 109, and 130% more ascorbic acid in BCG-10 applied treatment, respectively. The results of this experiment show that BCG-10 increased the growth and physiological traits of rice plants were exposed to different levels of salt stress. This was achieved by lowering hydrogen peroxide levels, making plant cells more stable, and increasing non-enzymatic activity. [Display omitted] • Biochar with gypsum improved the rice physiological parameters under salinity conditions. • Biochar with gypsum enhanced plant cell progression cycle. • Biochar with lime, and farm manure shows a relatively minimal response than gypsum. • The biochemical analyses revealed reduced oxidative stress in rice plants by applying biochar and gypsum. • The findings offer promising avenues for optimizing crop performance in salt-affected soil. [ABSTRACT FROM AUTHOR]

Enhancing the kinetic performance of thick electrodes is essential for improving the efficiency of lithium extraction processes. Biochar, known for its affordability and unique three-dimensional (3D) structure, is utilized across various applications. In this study, we developed a biochar-based, 3D-conductive network thick electrode (∼20 mg cm−2) by in-situ deposition of LiFePO 4 (LFP) onto watermelon peel biomass (WB). Utilizing Density Functional Theory (DFT) calculations complemented by experimental data, we confirmed that this The thick electrode exhibits outstanding kinetic properties and a high capacity for lithium intercalation in brines, even in environments where the Magnesia-lithium ratios are significantly high. The electrode showed an impressive intercalation capacity of 30.67 mg g−1 within 10 min in a pure lithium solution. It also maintained high intercalation performance (31.17 mg g−1) in simulated brines with high Magnesia-lithium ratios. Moreover, in actual brine, it demonstrated a significant extraction capacity (23.87 mg g−1), effectively lowering the Magnesia-lithium ratio from 65 to 0.50. This breakthrough in high-conductivity thick electrode design offers new perspectives for lithium extraction technologies. The watermelon peel serves as the substrate, simultaneously supporting the in-situ loading of LFP, thereby forming an LFP/WB thick electrode exhibits high lithium absorption capacity and excellent kinetic performance in high Mg2+/Li+ ratio brine. It achieved an impressive absorption rate of 30.67 mg g−1·min−1 in 10 min and an average lithium extraction of 23.87 mg g−1 from salt lake brine. This approach effectively reduced the Mg2+/Li+ ratio from 65 to 0.50, enabling efficient lithium separation and comprehensive biological resource utilization. [Display omitted] • The comprehensive utilization of biological resources is achieved. • The low efficiency of Li + extraction with thick electrode is effectively solved. • Effectively reducing the Mg2+/Li+ ratio in low-grade brine. [ABSTRACT FROM AUTHOR]