Biochar最新文献

The present study aimed to accelerate the humification and to investigate how MnO₂ modification of biochar (MBC) drives the humus formation during composting with chicken manure. In this study, compared with the control group (CK), the addition of MBC caused an increase in the concentration of both humus and humic acid (HA), with a respective enhancement of 29.1% and 37.2%. In addition, MBC also improved the stability of compost products. Hetero two-dimensional correlation spectra further exhibited that the MBC could alter the formation mechanism of humus fractions during composting. Random forest analysis showed that Microbacterium, Bacteroides, Kroppenstedtia, Gracilibacillus, and Lentibacillus were significantly related to humus formation (P < 0.05). MBC enhanced the absolute abundance of these five genera during composting. The structural equation model further confirmed that these five genera could be indirectly involved in humus formation, through the production of aromatic compounds via secondary metabolism. Additionally, these five genera could directly transform organic components into macromolecular humus structures. Therefore, the increase in these five genera might be a direct response to the acceleration of the humification during MBC composting. These findings demonstrate the potential value of MBC in harmless disposal of hazardous biowastes through composting.

Highlights

• MnO₂ modification of biochar changed the formation mechanism of humus fractions.

• Key genera involved in humus formation were identified.

• Among of MnO₂ modification of biochar, key genera and humus formation were revealed.

Graphical Abstract

This study investigated the effects of bamboo age, bamboo parts, and pyrolysis temperatures on the physiochemical properties of bamboo char throughout a series of pyrolysis processes spanning from 150 °C to 1000 °C. The results indicated that as the pyrolysis temperature increased from 150 °C to 500 °C, the yield of bamboo char experienced a rapid decline, settling at a maximum of 69%, with no significant impact from bamboo age and parts. Subsequently, as the pyrolysis temperature continued to rise from 500 °C to 1000 °C, the yield stabilized at 25.74–32.64%. Besides, fixed carbon (FC), volatile matter (VM), and ash content were temperature-dependent, while the H/C, O/C, (N + O)/C, and aromatic index kept constant after reaching 500 °C. Notably, 800 °C was confirmed to be a crucial turning point for physiochemical properties, at which the graphitic structural changes occurred, pore collapsed, and potassium salts released. Bamboo age was proved to enhance the stability. Pearson correlation coefficient (PCC) analysis revealed that the pyrolysis temperature was positively correlated (p < 0.01) with ash (0.76), FC (0.97), AI (0.81), R₅₀ (0.77), and C–C/C = C/C–H (0.87). Conversely, negative correlations (p < 0.01) were observed with VM (−0.91), O/C (0.88), H/C (−0.95), (N + O)/C (−0.87), C loss (−0.79), and labile organic-C (−0.78). Additionally, bamboo age was negatively correlated (p < 0.01) with C loss (−0.40), volatile organic-C (−0.63), labile organic-C (−0.45), and recalcitrant organic-C (−0.40), but positively associated with R₅₀ (0.54), refractory organic-C (0.42), and inorganic-C (0.52). Bamboo parts did not exhibit significant correlations with char properties.

Graphical Abstract

Pyrolysis is one method for treating sewage sludge, particularly in remote areas or decentralised systems. The end product of pyrolysis, sludge-char, can serve as a soil improver. However, there is a lack of comprehensive data on the organic pollutants’ behaviour in sludge-char. In our work, we focused on the behaviour of per- and polyfluoroalkyl substances (PFASs). Sludge was pyrolyzed at 200–700 °C to determine the minimum safe temperature for effective PFASs removal. It is important to note that PFASs may not only be mineralized but also cleaved to unanalyzed PFASs and other organofluorinated substances. To address this issue, we incorporated additional measurements of organic fluorine in the experiment using combustion ion chromatography (CIC). Due to the inherent heterogeneity of sludge, containing a variety of pollutants and their precursors, we conducted pyrolysis on artificially contaminated sand. This allowed us to assess and compare the behaviour of PFASs in a homogeneous matrix. Based on our analyses, we determined that a temperature greater than 400 °C is imperative for effective PFASs and organic fluorine removal. The results were verified by analyzing samples from a commercial sludge pyrolysis unit at the Bohuslavice-Trutnov WWTP, which confirmed our measurements. In light of these results, it becomes evident that sludge pyrolysis below 400 °C is unsuitable for PFAS removal from sewage sludge.

Graphical Abstract

Important properties of biochar as an effective soil amendment are its high water-holding capacity (WHC) and inhibition of water evaporation. However, the mechanism and the importance of biochar properties in controlling its own WHC and bound water evaporation remain little known. In this study, wheat straw and pine sawdust biochars were pyrolyzed in N₂-flow, CO₂-flow, and air-limitation environments at 300–750 ℃, and a series of the produced biochars’ properties were characterized to explore the dominant controlling factors of their WHC and bound water evaporation. The results have shown that with the increasing contents of hydrogen, nitrogen, and oxygen as well as such ratios as H/C, and (O + N)/C, WHC of the biochars was also increasing while the evaporation of biochar-bound water was decreasing. With an increase in the other studied factors, such as carbon content, pH, and specific surface area (SSA), WHC of the biochars was decreasing, and the evaporation of biochar-bound water was increasing. That was connected with the fact that biochar-nitrogen was mainly in pyridinic and pyrrolic forms, while oxygen was in the form of C = O and C–O bonds. These forms of nitrogen and oxygen could be the receptors of hydrogen bonds to link to H₂O molecules. Aliphatic hydrogen with a weak positive charge could be a donor of hydrogen bonds to link to H₂O molecules. However, high carbon content, as well as high SSA, indicated more exposed aromatic carbon (hydrophobic sites) that could suppress the binding of H₂O molecules. Additionally, high pH indicated that H₂O molecules were dominated by OH^–, which generated strong electrostatic repulsion with the negatively charged nitrogen- and oxygen-containing groups of biochar. It was also shown that the nitrogen-containing groups played a more important role (importance – 0.31) in WHC of the biochar than other parameters, including carbon, oxygen, hydrogen, ash contents, pH, SSA (importance from 0.02 to 0.09). Nitrogen, oxygen, and carbon contents had the most important influence on the evaporation of biochar-bound water in all studied factors. Furthermore, wheat straw biochar produced at low pyrolysis temperatures in N₂ atmosphere (with high nitrogen and oxygen contents) had the highest WHC and the lowest evaporation of biochar-bound water. Consequently, it can be suggested that biochar rich in nitrogen can be an effective water retention agent and can improve agricultural soil moisture.

Graphical Abstract

Arsenic (As) detoxification in polluted soils by iron-based materials can be mediated by the endogenous soil organic matter (SOM), nevertheless the mechanisms remain unclear. Herein, endogenous SOM in a paddy soil was substantially removed to understand its roles on As immobilization by biochar-supported zero-valent iron (ZVI/BC). The results demonstrated that ZVI/BC application significantly decreased As bioavailability by 64.2% compared with the control soil under the anaerobic condition. XPS and HR-TEM suggested As immobilization by ZVI/BC mainly invoked the formation of ternary complexes (i.e., As-Fe-SOM). However, SOM depletion compromised the efficacy of ZVI/BC for As immobilization by 289.8%. This is likely because SOM depletion increased the fulvic acid and OH⁻ contents in soils. Besides, ZVI/BC increased the proportion of As(III) in available As fraction, but SOM depletion altered the mechanisms associated with As(V) reduction. That is, As(V) reduction resulted from the reductive capacity of ZVI in the pristine soil, but the As(V)-reducing bacteria contributed greater to As(V) reduction in the SOM-depleted soil. Additionally, SOM depletion boosted the abundances of Fe(III)- and As(V)-reducing bacteria such as Bacillus and Ammoniphilus in soils, which enhanced the dissimilatory arsenate reduction. Thus, this work highlighted the importance of SOM in the remediation of As-contaminated soils by ZVI/BC.

Graphical Abstract

Abstract

The swift advancement of sustainable energy technologies, coupled with the urgent need to address environmental challenges, has generated considerable interest in the multifaceted applications of biochar materials to promote energy, water, and environmental sustainability. This comprehensive review examines recent advancements in the production and applications of functionalized biochar materials, emphasizing their pivotal roles in energy conversion and storage, wastewater treatment, CO₂ reduction, soil amelioration, and the promotion of carbon neutrality within a circular economy framework. The functionalization of biochar materials involves surface chemistry and porosity modifications, achieved through techniques like templating, chemical activation, metal impregnation, or heteroatom doping. These modifications substantially enhance the catalytic activity, energy storage capacity, and cycling stability of biochar materials, making them particularly effective in diverse energy applications such as water splitting, fuel cells, and supercapacitors. Additionally, functionalized biochar materials demonstrate remarkable efficacy as catalysts and adsorbents in wastewater treatment, proficiently removing pollutants like heavy metals, organic contaminants, and nutrients, thereby facilitating resource recovery from wastewater. The review also underscores the potential of functionalized biochar materials in CO₂ capture and conversion, exploring innovative strategies to augment their CO₂ adsorption capacity and state-of-the-art catalytic processes for transforming captured CO₂ into valuable fuels and chemicals. In summary, this review offers valuable insights into the recent advancements in biochar research, underscoring its substantial commercial potential as a versatile material contributing to a cleaner and more sustainable future.

Article Highlights

• The current status of biochar research is comprehensively reviewed.

• The potential of biochar in energy, water, and environmental fields is critically examined.

• Technology readiness levels (TRLs) of various biochar-based technologies are evaluated.

The global environmental issue of soil contamination with antibiotic-resistance genes has garnered increased attention in recent years due to its impact on ecosystems and human health. Despite this recognition, researchers face challenges in comprehensively understanding the mechanisms underlying the production and dissemination of soil resistance genes, particularly in relation to their implications for human health. This lack of understanding poses a barrier to the development of effective and precise control strategies. Biochar, a sustainable material, exhibits favorable adsorption properties characterized by its large pores and specific surface area. Therefore, we propose to explore the potential application of biochar addition in soil resistance gene management. In order to establish a solid research foundation in this area, in this paper we review the mechanisms underlying the generation and accumulation of soil resistance genes over the last decade, along with their transmission pathways and interfacial interactions. Biochar may help repair soil resistance genes by affecting factors like antibiotic levels, environmental conditions, enzymatic activity, and gene migration mechanisms, opening up new research possibilities.

Graphical Abstract

Anaerobic digestion (AD) was initially evaluated as a potential preprocessing method for preparing biomass-based carbon electrocatalysts in this study. The AD pretreatment succeeded in the structural depolymerization and nitrogen enrichment of Hybrid Pennisetum, which provided favorable conditions to achieve efficient and homogeneous nitrogen introduction due to microorganism community enrichment and provided a porous structure by degradation of the biodegradable components. The resulted biochar exhibited improved physiochemical properties including higher specific surface areas, nitrogen content and graphitization degree than that obtained from pyrolyzing raw biomass. These improvements were positively correlated with the AD time and showed to have enhanced the performance in oxygen reduction reaction and practical microbial fuel cell applications. Amongst the investigated samples, the obtained biochar pretreated by AD for 15 days exhibited the most excellent performance with an onset potential of 0.17 V (VS. saturated calomel electrode) and the maximal power density of 543.2 mW cm⁻² assembled in microbial fuel cells. This study suggested applying AD as a new biological pretreatment in the preparation of biomass-based electrocatalysts, and provided a unique pathway for fabricating high-performance biochar-based catalysts by structure optimization and N-containing active sites construction via gentle biological method, thereby providing a cost-effective method to fabricate metal-free catalysts for oxygen reduction reaction.

Graphical Abstract

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

Graphical Abstract