Biochar最新文献

Biochar is a carbon-rich material produced through the pyrolysis of various feedstocks. It can be further modified to enhance its properties and is referred to as modified biochar (MB). The research interest in MB application in soil has been on the surge over the past decade. However, the potential benefits of MB are considerable, and its efficiency can be subject to various influencing factors. For instance, unknown physicochemical characteristics, outdated analytical techniques, and a limited understanding of soil factors that could impact its effectiveness after application. This paper reviewed the recent literature pertaining to MB and its evolved physicochemical characteristics to provide a comprehensive understanding beyond synthesis techniques. These include surface area, porosity, alkalinity, pH, elemental composition, and functional groups. Furthermore, it explored innovative analytical methods for characterizing these properties and evaluating their effectiveness in soil applications. In addition to exploring the potential benefits and limitations of utilizing MB as a soil amendment, this article delved into the soil factors that influence its efficacy, along with the latest research findings and advancements in MB technology. Overall, this study will facilitate the synthesis of current knowledge and the identification of gaps in our understanding of MB.

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Biochar, produced from the thermochemical conversion of biomass waste, has various applications owing to its broad utility and advantageous properties. This study employs a scientometric approach to comprehensively assess the advancements in biochar application from 2022 to 2023. Utilizing 13,357 bibliographic records sourced from the Web of Science Core Collection with the search term “biochar”, the analysis focuses on authorship, national contributions, and keyword trends. Findings demonstrate a continual rise in annual publications since 2009, albeit with a moderated growth rate in 2023. China leads in publication outputs, followed by USA and India, with Hailong Wang emerging as a prominent figure in biochar research. Keyword co-occurrence analyses identify key research themes such as biochar’s role in climate change mitigation, easing salinity and drought stress, immobilizing toxic metals, degrading organic pollutants, serving as additives in anaerobic digestion, and functioning as electrodes in microbial fuel cells. Among these, biochar’s application for global climate change mitigation gains significant attention, while its utilization as electrodes in microbial fuel cells emerges as a promising research frontier, indicating the growing need for sustainable energy sources. The study also outlines critical research gaps and future priorities for enhancing biochar application. Overall, it highlights the diverse applicability of biochar and offers valuable insight into research progression and forthcoming directions in biochar studies.

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Low-cost and green preparation of efficient sorbents is critical to the removal of organic contaminants during water treatment. In this study, the co-pyrolysis of macroalgae and oyster shell was designed to synthesize nitrogen-doped porous biochars for sorption removal of atrazine from water. Oyster shell played a significant role in opening pores in macroalgae-derived biochars, resulting in the surface area of the macroalgae (Enteromorpha prolifera and Ulva lactuca) and oyster shell co-pyrolyzed carbonaceous as high as 1501.80 m² g⁻¹ and 1067.18 m² g⁻¹, the pore volume reached 1.04 cm³ g⁻¹ and 0.93 cm³ g⁻¹, and O/C decreased to 0.09 and 0.08, respectively. The sorption capacity of atrazine to nitrogen-doped porous biochars (the Enteromorpha prolifera, Ulva lactuca and oyster shell co-pyrolyzed carbonaceous) reached 312.06 mg g⁻¹ and 340.52 mg g⁻¹. Pore-filling, hydrogen bonding, π-π or p-π stacking and electrostatic interaction dominated the multilayer sorption process. Moreover, the nitrogen-doped porous biochars showed great performance in cyclic reusability, and the Enteromorpha prolifera, Ulva lactuca and oyster shell co-pyrolyzed carbonaceous sorption capacity still reached 246.13 mg g⁻¹ and 255.97 mg g⁻¹, respectively. Thus, this study suggested that it is feasible and efficient to remove organic contaminants with the nitrogen-doped porous biochars co-pyrolyzed from macroalgae and oyster shell, providing a potential green resource utilization of aquatic wastes for environmental remediation.

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Phosphorus-modified biochar has been proven to enhance the precipitation and complexation of heavy metal ions from wastewater. However, the current modification methods require large amounts of exogenous P and have high energy consumption. Hence, this study proposes and analyzes a strategy integrating biochar production, phosphorus wastewater treatment, dephosphorization waste recovery, and heavy metal removal. “BC-Ca-P” was derived from Ca-modified biochar after phosphorus wastewater treatment. The adsorption of Pb(II) by BC-Ca-P followed the Langmuir isotherm and pseudo–second–order kinetic models. The maximum adsorption capability of 361.20 mg·g⁻¹ at pH 5.0 for 2 h was markedly greater than that of external phosphorous-modified biochar. The adsorption mechanisms were dominated by chemical precipitation and complexation. Furthermore, density functional theory calculations indicated that oxygen-containing functional groups (P-O and C-O) contributed the most to the efficient adsorption of Pb(II) onto BC-Ca-P. To explore its practical feasibility, the adsorption performance of BC-Ca-P recovered from an actual environment was evaluated. The continuous-flow adsorption behavior was investigated and well-fitted utilizing the Thomas and Yoon–Nelson models. There was a negligible P leakage risk of BC-Ca-P during heavy metal treatment. This study describes a novel and sustainable method to utilize dephosphorization waste for heavy metal removal.

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Biochar (BC) applications in soil has positive effects on plant performance, particularly for loose soil in agricultural context. However, how biochar types affect plant performance of non-crop species and soil–plant carbon relationships is not clear. We selected five different BC types and three plant species to investigate the responses of plant performance and the soil–plant carbon relationship to BC effects. The result demonstrated that peanut shell BC led to the death of both R. tomentosa and C. edithiae, due to a reduction in nutrient uptake caused by higher soil electricity conductivity (2001.7 and 976.3 µS cm⁻¹). However, the carbon content of S. arboricola increased by 57% in peanut shell BC-amended soil, suggesting that S. arboricola has a higher tolerance for soil salinity. Wood BC-amended soil led to better stomatal conductance (g_s) and leaf area index (LAI) of both R. tomentosa and C. edithiae due to the higher water retention in the soil (22.68% and 20.79%). This illustrated that a higher amount of water retention brought by wood BC with a great amount of pore volume might be the limited factor for plant growth. The relationship between g_s and LAI suggested that g_s would not increase when LAI reached beyond 3. Moreover, wood and peanut shell BC caused a negative relationship between soil organic carbon and plant carbon content, suggesting that plants consume more carbon from the soil to store it in the plant. Overall, wood BC is recommended for plant growth of R. tomentosa and C. edithiae, and peanut shell BC is suggested for S. arboricola carbon storage.

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Hydrothermal carbonization (HTC) stands out as an eco-friendly, cost-effective method for generating renewable carbon-based materials from biomass. The HTC process yields products such as hydrochars and carbon dots (CDs), possessed of notable photocatalytic capabilities due to their unique physicochemical features. Additionally, pairing traditional photocatalysts with hydrochar derivatives elevates their performance, rendering them more effective. Recent times have witnessed a surge in interest in these hydrochar based photocatalysts (HC-photocatalysts). Their appeal stems from multiple attributes: impeccable performance, adaptability to visible light, and adjustable physicochemical properties. This review delves deep into the evolving landscape of these HC-photocatalysts, segmenting them into three distinct categories: hydrochars, hydrochar-based CDs (HC-CDs), and hydrochar-based composites (HC-composites). For each category, we dissect their synthesis routes, unravel the photocatalytic mechanisms, and explore various enhancement strategies. We further traverse their versatile applications, spanning environmental treatment, disinfection, energy conversion, and organic synthesis. In the end, we spotlight the prevailing challenges and uncharted territories in the domain of HC-photocatalysts. In essence, this review serves as a guide, furnishing a theoretical foundation and steering directions for future explorations and tangible implementations of HC-photocatalysts.

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Vermicomposting utilizes the synergistic effect of earthworms with microorganisms to accelerate the stabilization of organic matter in biowastes. Nevertheless, the exact mechanism behind the maturity of vermicompost and the growth of earthworms exposed to biochar of varying particle sizes remains unclear. This study presents an investigation of the effect of biochar particle size on earthworm (Eisenia fetida) survival, microbial diversity, and the quality of vermicompost products. To address these issues, pelletized dewatered sludge samples from a municipal sewage treatment plant were amended with pine-based biochar with particle sizes of 1–2 mm, 25–75 μm, 200 nm, and 60 nm as the substrate for vermicomposting. This study revealed that the addition of millimeter-scale biochar and micron-scale biochar significantly promoted the degradation of organic matter since the organic matter in the treatment with 1–2 mm biochar at the end of the vermicomposting experiment decreased by 12.6%, which was equivalent to a 1.9-fold increase compared with that of the control. Excessive nanopowdering of nanobiochar significantly affected the survival of earthworms and led to 24.4–33.3% cumulative mortality, while millimeter-scale (mm) biochar and micron-scale (μm) biochar achieved zero mortality. The findings of this study could be used for evaluating the potential impact of nanoscale biochar to earthworms and guiding biochar-augmented vermicomposting.

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Crop residues and their derived biochar are frequently used for their potential to improve grain yield, soil fertility and carbon (C) sequestration. However, the effects of root are often overlooked, and the effects of chemical fertilizer (NPK) combined with root or its biochar on microbial community structure need further study. This study used ¹³C-labeled maize root, its biochar and soil with different fertilization for 8 years as materials and substrates. A 112-day incubation experiment was conducted to explore the effects of microbial community on the C processing. During incubation, the root-C (54.9%) mineralized significantly more than biochar-C (12.8%), while NPK addition significantly increased the root-C mineralization. Adding biochar alone did not significantly change the microbial community. Compared to the biochar treatment (BC), the root treatment (R) notably increased the contents of total phospholipid fatty acids (PLFAs), ¹³C-PLFA and the proportion of fungi and Gram-negative bacteria, but reduced the proportion of actinomycetes. The root mineralization was significantly correlated with the relative content of ¹³C-Gram-positive bacteria and ¹³C-fungi, while biochar mineralization was significantly correlated with the relative content of ¹³C-Gram-positive bacteria and ¹³C-actinomycetes. Notably, NPK addition significantly increased the contribution of biochar-C to PLFA-C pool, while decreasing the contribution of root-C. In summary, due to microbial adaptation to the lack of bioavailable C in biochar-amended soil, biochar can act as a buffer against the significant disturbance caused by NPK to microbial communities and native soil organic carbon (SOC), which contributes to the steady enhancement in soil C storage.

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Co-hydrothermal carbonization (co-HTC) of phosphorus rock (PR) and corn straw (CS) was investigated to prepare hydrochar-based materials as soil conditioners, focusing on the morphological transformation and solid–liquid migration of carbon and phosphorus. Various analytical methods, including elemental analysis, chemical quantification, FT-IR, XRD, 3D-EEM, TG, and XANES, were used to understand the synergistic interactions of PR and CS during co-HTC and determine the properties of the resultant products. The results indicated the acidic solution and humic acid-like substances produced by HTC of CS reduced the crystallinity of the PR and served as the activating agent for PR, allowing the PR to be easily dissolved and reconstituted, producing calcium carbonate and apatite-like materials, and the formation of C–O–PO₃, C–PO₃, C=O, and O=C–O chemical bonds. At 220 °C, adding 5% PR significantly promoted a 10.3% rise in the yield of CS hydrochar, a 4.3% rise in carbon recovery of CS, and a 4.8% rise in carbon sequestration potential of CS. The formation of Ca–P was notably promoted and the content of AP in co-HTC hydrochar was up to 89.9%, with 39% Hydro-P and 33% CaHPO₄. In the case of artificial humic acid (HAa), its content was also remarkably increased by 5.9% in the hydrochar by co-HTC. In addition, the hydrochar produced by co-HTC of CS and PR was composed of carbon with an increased aromatic degree, rich organic matter, and biologically effective mineral nutrient elements and exhibited high stability. The present study provided a promising approach for value-added utilization of waste biomass and low-grade PR towards soil application.

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To reveal the influence of the diversity of precursors on the formation of environmental persistent free radicals (EPFRs), pomelo peel (PP) and its physically divided portion, pomelo cuticle (PC), and white fiber (WF) were used as precursors to prepare six hydrochars: PPH-Fe, PCH-Fe, WFH-Fe, PPH, PCH, and WFH with and without Fe(III) addition during hydrothermal carbonization (HTC). PPH-Fe and WFH-Fe had higher EPFRs content (9.11 × 10¹⁸ and 8.25 × 10¹⁸ spins·g⁻¹) compared to PPH and WFH (3.33 × 10¹⁸ and 2.96 × 10¹⁸ spins·g⁻¹), indicating that iron-doping favored EPFRs formation. However, PCH-Fe had lower EPFRs content (2.78 × 10¹⁸ spins·g⁻¹) than PCH (7.95 × 10¹⁸ spins·g⁻¹), possibly due to excessive iron leading to the consumption of the generated EPFRs. For another reason, the required Fe(III) amount for EPFRs formation might vary among different precursors. PC has a lower concentration of phenolic compounds but 68–97% fatty acids, while WF and PP are rich in cellulose and lignin. In the Fenton-like reaction, oxygen-centered radicals of hydrochar played a significant role in activating H₂O₂ and efficiently degrading bisphenol A (BPA). Mechanisms of reactive oxygen species (ROS) generation in hydrochar/H₂O₂ system were proposed. EPFRs on hydrochar activate H₂O₂ via electron transfer, creating ·OH and ¹O₂, leading to BPA degradation. More importantly, the embedded EPFRs on the hydrochar's inner surface contributed to the prolonged Fenton-like reactivity of PPH-Fe stored for 45 days. This study demonstrates that by optimizing precursor selection and iron doping, hydrochars can be engineered to maximize their EPFRs content and reactivity, providing a cost-effective solution for the degradation of hazardous pollutants.

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