Structure Of Biochar Research Articles

Pistia stratiotes L. Biochar for Sorptive Removal of Aqueous Inorganic Nitrogen.

Biochar has proven effective in the remediation of excess nitrogen from soil and water. Excess nitrogen from agricultural fields ends up in aquatic systems and leads to reduced water quality and the proliferation of invasive species. This study aimed to assess the efficiency of chemically surface-modified biochar produced from invasive Pistia stratiotes L. for the adsorption of inorganic nitrogen (NH4+ and NO3-). Biochar structure was investigated using scanning electron microscopy, energy-dispersive X-ray analysis, X-ray photoelectron spectroscopy, Fourier-transform infrared spectroscopy, and inductively coupled plasma mass spectrometry. The results from adsorption experiments indicate that NH4+ removal was optimal (0.8-1.3 mg N g-1) at near-neutral pH levels (6.0-7.5), while NO3- removal was optimal (0.4-0.8 mg N g-1) under acidic pH conditions (4.8-6.5) using the modified biochar. These findings highlight the significance of solution pH, biochar morphology, and surface chemistry in influencing the adsorption of NH4+ and NO3-. However, further studies are necessary to assess the potential oxidative transformation of NH4+ to NO3- by biochar, which might have contributed to the reduction in NH4+ in the aqueous phase.

Simplified oxygen-limited thermal treatment without tube furnace and inert gas

The article introduces a cost-effective and user-friendly alternative to traditional pyrolysis techniques, obviating the necessity for intricate tube furnaces and inert gas environments. This novel approach employs materials capable of reacting with and sequestering oxygen to establish an oxygen-depleted atmosphere. The experimental setup entails positioning a crucible containing the sample inside a ceramic pot, enveloped by varying sizes of wood coal particles, and subsequently subjecting the ceramic pot to furnace conditions. Utilizing this oxygen-limited strategy, a biochar sample, derived via hydrothermal processing, underwent carbonization at 650°C for 6.5 hours, with outcomes compared against ambient condition carbonization under identical temperature and duration parameters. Gravimetric analysis revealed that wood coal effectively curtails oxygen availability, augmenting biochar yield from 1.53 % to 19.50 %. Fourier-transform infrared spectroscopy (FTIR) indicates diminished oxygen functional groups, while X-ray diffraction (XRD) and field-emission scanning electron microscopy (FESEM) affirmed a denser, compact carbon structure in biochar produced under oxygen-restricted conditions versus ambient conditions. The carbon content percentage in biochar samples treated at 650°C for 6.5 hours under both conditions was assessed via energy-dispersive X-ray spectroscopy (EDX) data. The emergence of a novel carbon nanomaterial, derived from biomass waste through our oxygen-limiting method, may exhibits applications in energy storage and water purification. Our approach offers simplicity, cost-efficiency, and straightforward implementation while upholding the integrity of pyrolysis/thermal treatment within inert conditions, ensuring the robustness of the procedure.

Co-regulating the pore structure and surface chemistry of sludge-based biochar for high–performance deodorization of gaseous dimethyl disulfide

A straightforward and eco-friendly preparation method for porous sludge biochar (SBA-3) was developed to deodorize gaseous dimethyl disulfide (DMDS) using ion exchange to adjust micropore structures coupled with carboxyl functionalization. Compared with the unmodified sludge biochar SBA-1 and SBA-2 treated with ion exchange, the pore size of SBA-3 decreased accompanied with increasing specific surface area and micropore volume. The Brunauer–Emmett–Teller (BET) specific surface area and micropore volume were 176.35 m2 g−1 and 0.0314 cm³ g−1, which were 2.02 and 1.71-fold larger than those of SBA-2, as well as 20.60 and 78.5-fold larger than those of SBA-1, respectively. Meanwhile, the amount of –COOH on the surface of SBA-3 increased from 0.425 to 1.123 mmol g−1, which was 2.64-fold larger than that of SBA-1. The adsorption behavior between DMDS and SBA-3 could be well described by the quasi-second-order kinetic model and Langmuir isotherm model. The maximum monolayer adsorption capacity was 35.12 mg g−1 at 303 K. Thermodynamic and DFT calculations indicated that the adsorption of DMDS on SBA-3 was exothermic with the deodorization mechanisms involving pore filling and chemisorption.

Biochar-based persulfate activation: Rate constant prediction, key variables identification, and system optimization

Biochar has emerged as a promising sustainable catalyst for persulfate-based advanced oxidation processes (PS-AOPs), offering synergy between radical and non-radical pathways for superior mineralization. To streamline the traditionally time-consuming and costly biochar selection process, artificial intelligence was employed for a more efficient approach. In this study, an extreme gradient boosting (XGB) model was used to predict the pseudo-first-order kinetic rate constant (k) of a PS-AOPs. Important features were analyzed, and optimal feature values were obtained using particle swarm optimization (PSO). The dataset comprised 671 data points with 18 features extracted from peer-reviewed publications. To address data sparsity and imbalance, machine learning techniques and stratified data splits were utilized, achieving high model performance (R2 = 0.96, RMSE = 0.035). Feature importance analysis using XGB, permutation feature importance, and SHapley Additive exPlanations highlighted the importance of a higher biochar oxygen-to‑carbon ratio and encouraged metal modification. The presence of oxygen functional groups, particularly carbonyl and graphitized biochar structures, was emphasized in kinetic performance. PSO results recommended optimized biochar preparation parameters and operating conditions to enhance the k value, aligning with existing literature. This study predicts kinetic outcomes under preset conditions and guides practical biochar selection, demonstrating its relevance and potential in real-world applications.

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

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

Amino/MnO2 combined modified biochar for enhancing Pb2+ and Cd2+ removal and mechanisms from aqueous solution

Heavy metals from aqueous solutions tend to pose toxicity to the environment, hence it is urgent to treat this pollution. Current studies have exhibited the adsorption capacity of original biochar for Pb2+ and Cd2+ in water, while effective methods were lacking to enhance its adsorption capacity and alleviate competitive adsorption. In this study, MnO2 and amino group combined modification was proposed to improve the Pb2+ and Cd2+ adsorption capacity of rice straw-derived biochar (MNBC) in water. The adsorption performances and mechanisms of MNBC were obtained from batch experiments, several characterizations, and DFT calculation. The results found that modified methods rose the variety of functional groups variety and improved the pore structure of biochar. Maximum removal rates for Pb2+ and Cd2+ were 96.18 % and 64.26 % and still reached 87.6 % and 54.4 % after four cycles in single Pb2+ or Cd2+ system. Cation exchange as well as electrostatic attraction might the main adsorption mechanism in the Pb2+ and Cd2+ adsorption process. In binary system, theoretical calculation exhibited that electron cloud neared Pb was more possible to transfer with adsorbent than that of Cd, which was accordance to the results of competitive adsorption. The p orbital of O atom in MnO2 and N orbital atom in amino groups could hybridize with d orbital of Cd and Pb, which effectively reduced the effect of competitive adsorption. Overall, this study proved removal prospect of MNBC for Pb2+ and Cd2+ and its highly efficient and stable in application.

Study on the synergistic hydrogen production performance and mechanism of NiO/WO3-biochar composite material in the photocatalytic 5-hydroxymethylfurfural conversion to 2,5-furandicarboxylic acid

In this work, a simple hydrothermal synthesis method is used to prepare photocatalytic NiO/WO3-biochar composite material, which is applied to catalyze the one-step conversion of 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid with synergistic hydrogen production. The optoelectronic properties of NiO/WO3-biochar composite material are characterized. The results indicate that the p-n heterojunction-coupled biochar structure between NiO and WO3 in the NiO/WO3-biochar composite is an important prerequisite for ensuring the one-step oxidation reaction of 5-hydroxymethylfurfural. The experimental results reveal the possible reaction pathways. Under the optimal ratio of NiO/WO3-biochar composite material, the 5-hydroxymethylfurfural conversion rate reaches 100%, the 2,5-furandicarboxylic acid yield reaches 99.6%, and the Faraday efficiency of hydrogen evolution is 98%. This study provides a new approach for the one-step photocatalytic synthesis of 2,5-furandicarboxylic acid from 5-hydroxymethylfurfural, as well as a novel and efficient catalyst for photocatalytic oxidation technology.

Coupled effects of Fenton-like systems with different concentrations of H2O2/Biochar on diethyl phthalate removal: Dominant role of environmental persistent free radicals (EPFRs)

To investigate the impact of different H2O2 concentrations on the Fenton-like systems of H2O2/biochar, this study examined the mechanism of the physical structure and environmental persistent free radicals (EPFRs) of biochar during diethyl phthalate (DEP) removal by the Fenton-like system. The peak-splitting method was utilized to differentiate EPFRs types in cotton stalk biochar produced at different temperatures. High-temperature environments promote π-electron delocalization, which facilitates phenyl π free radicals and σ-π oxygen-containing free radicals. By analyzing relationships between the removal rate K1 and removal constant Kobs of DEP with the structural properties of biochar, it was discovered that EPFRs concentrations in biochar had a significant positive correlation with K1 (r = 0.92) and Kobs (r = 0.97). Different H2O2 concentrations added to the biochar removal system resulted in varied DEP removal efficiency. Among them, CS500, CS550, and CS600 exhibited superior DEP removal efficiency when H2O2 concentration was 5 mM.

Use of biochar as a catalyst for biodiesel production

The economic viability of biodiesel (BD) production is highly dependent on conversion techniques using inexpensive oil feedstocks. In this study, BD was synthesised by the thermally induced (non-catalytic) transesterification of oil extracted from camellia seed (42.23 wt% lipid content). The BD yield from the non-catalytic transesterification of camellia oil was higher than that from the alkali-catalysed process. The BD yield from the alkali-catalysed transesterification of camellia oil for 60 min was 84.1 wt%, whereas that from the non-catalytic process for ≤ 1 min at 360 ˚C was 93.5 wt%. To realise a virtuous circle in the production of BD, this study sought a strategic way to valorise oil-extracted biomass waste (lignocellulose-based). Specifically, this study sought a method for valorising biochar as an effective catalyst, hypothesizing that earth alkaline metals finely dispersed within the porous structure of biochar would effectively enhance catalytic capability. The BD yield in the presence of camellia biochar was 92.4 wt% (saturated at ≥ 240 ˚C). Thus, the reaction kinetics for the transesterification of camellia oil over camellia biochar was catalytically accelerated. Such efforts provide opportunities to enhance economic viability and realise the concept of a sustainable cycle in BD production.

Interconnected pyrolysis and activation with in-situ H3PO4 activation of biochar from pear wood chips in a pilot scale dual fluidized bed

Interconnected pyrolysis and activation is a novel technology for combustible gas and biochar production in dual fluidized bed (DFB). The study proposed one-step and two-step methods for pyrolysis and activation of biomass in a pilot scale DFB with capacity of 100 kg/h. Physical and chemical activation occurred simultaneously in DFB system by phosphoric acid (H3PO4) impregnation pretreatment of pear wood chips, and flowing hot flue gas and steam. Stable operating parameters were observed for both methods. The one-step method was superior to the two-step method in terms of the pyrolysis gas quality, biochar pore distribution, micro- and meso-pores structures of biochar, while one-step method reduced the biochar yields. As an activation agent, H3PO4 increased the yields of biochar and pyrolysis gas, promoted formation of micropores and enriched the surface functional groups of biochar with increasing ratio of H3PO4. H3PO4 to biomass ratio of 1:5 reached the maximum biochar yield of 42.3 wt% and highest iodine adsorption value of 648.5 mg/g, increasing by 70.6 % and 90.3 % compared to the biochar without H3PO4 pretreatment, respectively. This DFB system facilitated the diversified use of fluidized beds and the co-production of biochar and product gas with energy saving and CO2 emission reduction.

Microbial etch: A novel construction method of functionalized biochar for enhanced uranium extraction in radioactive wastewater

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.

Development of a Microwave-Assisted Bench Reactor for Biomass Pyrolysis Using Hybrid Heating.

Microwave-assisted pyrolysis (MAP) is a cutting-edge technology that converts biomass into fuels, chemicals, and materials. In this study, an Arduino was used to control and automate a MAP system built from a microwave oven with a cordierite chamber filled with silicon carbide. Sugar cane bagasse was pyrolyzed at 250, 350, 450, and 550 °C to validate the MAP system and obtain pyrolytic products with different yields and chemical compositions. Lower temperatures led to high biochar yields, but the highest surface area of 25.14 m2 g-1 was only achieved at 550 °C. By contrast, higher temperatures favored the recovery of pyrolysis liquids. BET and scanning electron microscopy analyses revealed a porous biochar structure, while Fourier transform infrared spectroscopy analysis showed that the availability of functional groups on the biochar surface decreased with an increase in pyrolysis temperature. GC-MS analysis quantified valuable low molecular mass compounds in pyrolysis liquids, including aldehydes, ketones, phenols, and alcohols. With its unprecedented hybrid heating device, the MAP system promoted suitable heating rates (31.9 °C min-1) and precise temperature control (only 19 °C of set point variation), generating pyrolysis products devoid of microwave susceptor interferences. Therefore, MAP provided a rapid, safe, and efficient means of depolymerizing biomass, thus holding promise for biorefinery applications.

Facile Recycling of Waste Biomass for Preparation of Hierarchical Porous Carbon with High-Performance Electromagnetic Wave Absorption.

Hierarchical-porous-structured materials have been widely used in the field of electromagnetic wave (EMW) absorption, playing a critical role in minimizing EMW interference and pollution. High-quality EMW absorbers, characterized by a lower thickness, lighter weight, wider absorption band, and stronger absorption capacity, have been instrumental in reducing damage and preventing malfunctions in the automotive and aviation industries. The utilization of discarded nut shells through recycling can not only alleviate environmental problems but relieve resource constraints. Herein, a facile method for the preparation of hierarchical porous biomass carbon derived from abandoned Xanthoceras Sorbifolium Bunge Shell (XSS) biomass was developed for high-performance EMW absorption. The porous structures of XSS biochar were studied by using different levels of the K2CO3 activator and simple carbonization. The effect of K2CO3 on the EMW parameters, including the complex permittivity, complex permeability, polarization relaxation, and impedance matching, was analyzed. The best EMW absorption performance of the XSS biochar was observed at a mass ratio of activator-to-biomass of 2:1. A minimum reflection loss (RLmin) of -38.9 dB was achieved at 9.12 GHz, and a maximum effective absorption bandwidth (EABmax) of up to 3.28 GHz (14.72~18.0 GHz) could be obtained at a 1.8 mm thickness. These results demonstrated that hierarchical porous XSS carbon was prepared successfully. Simultaneously, the prepared XSS biochar was confirmed as a potential and powerfully attractive EMW-absorbing material. The proposal also provided a simple strategy for the development of a green, low-cost, and sustainable biochar as a lightweight high-performance absorbing material.

Remediation of arsenic and fluoride from groundwater: a critical review on bioadsorption, mechanism, future application, and challenges for water purification.

In the past few decades, the excessive and inadequate use of technological advances has led to groundwater contamination, mainly caused by organic and inorganic pollutants, which are highly harmful to human health, agriculture, water bodies, and aquaculture. Among all toxic pollutants, As and F- play a significant role in groundwater contamination due to their excellent reactivity with other elements. To mitigate the prevalence of arsenic and fluoride within the water system, the use of biochar gives an attractive strategy for removing them mainly because of the substantial surface area, pore size, pH, aromatic structure, and functional groups inherent in biochar, which are primarily dependent upon its raw material and pyrolysis temperature. Researcher develops different methods like physiochemical and electrochemical for treating arsenic and fluoride contamination. Among all removal methods, bioadsorption using agricultural waste residues shows effective/feasible removal of As and F- due to its low cost, ecofriendly nature, readily available, and efficient reuse compared with several other harmful synthetic materials that demand costly design specifications. This study discusses current developments in bioadsorption methods for As and F- that use agricultural-based biomaterials and describes the prevailing state of arsenic and fluoride removal strategies that use biomaterials precisely.

Preparation of mesoporous biogas residue biochar via a self-template strategy for efficient removal of ciprofloxacin: Effect of pyrolysis temperature

Biochar preparation and application is an anticipated pathway for the resource utilization of biogas residue. In this study, biochars were prepared by the pyrolysis of biogas residue from food waste anaerobic digestion (named as BRBCs) under various pyrolysis temperatures (300, 500, 700, and 900 °C), and the effect of pyrolysis temperatures on the physicochemical characteristics of BRBCs was examined. The adsorption performance toward ciprofloxacin (CIP), a typical antibiotic in waterbodies, was also investigated. The results showed that pyrolysis temperature significantly changed the physicochemical properties of BRBCs. In addition, the minerals in the biogas residue, especially SiO2, were rearranged to form a mesoporous structure in biochar through a self-template strategy (without activator). BRBC prepared at 900 °C exhibited a high specific surface area and pore volume, well-developed mesopore structure, and more carbon structure defects, and exhibited the largest CIP adsorption capacity with 70.29 mg g−1, which was ascribed to the combined interaction of pore diffusion, π–π interactions, hydrogen bonding, complexation, and electrostatic forces. Furthermore, the adsorption of CIP by BRBC900 was well described by two-compartment kinetic and Langmuir isotherm models. BRBC900 showed good adsorption performance toward CIP at pH 7–9. The adsorption of CIP by BRBC is a spontaneous, exothermic, entropy-increasing process. Moreover, BRBC also presented a good recycling potential. Therefore, the preparation of mesoporous biochar based on a self-template strategy not only provides an option for the resource utilization of biogas residue but also offers a new option for the treatment of antibiotic wastewater.

Influence of different pyrolysis temperatures on chemical composition and graphite-like structure of biochar produced from biomass of green microalgae Chlorella sp

There is a great demand for environmentally friendly carbon materials as an alternative to fossil raw materials in industrial production. Microalgae biomass can be a valuable renewable source for the production of biochar. The study examined the effect of the pyrolysis temperature on the chemical composition, morphological features and the degree of order of the carbon structure of biochar based on green microalgae – Chlorella sp. Thermochemical conversion was carried out at 400÷900 °C in a CO2 atmosphere. The obtained biochar material had a porous structure. It was found that as the temperature increased, the biochar yield decreased from 38.4 to 21.9 wt%, while its aromaticity and stability, determined by the H/C molar ratio, increased. Based on the results of FTIR and Raman spectroscopy, it was evidenced that the biochar produced at 400÷500 °C was distinguished by the presence of functional groups and double bonds (i.e. –NH2, C–O, CC, CN, NO) as well as a high degree of order in the carbon structure (ID/IG=0.2). As the temperature increases, the amorphous nature of biochar began to develop. This study could provide data for the proper selection of temperature for pyrolysis of green algae to obtain biochar with the desired graphite-like structure and properties.

Effects of different precursors on the structure of lignin-based biochar and its ability to adsorb benzopyrene from sesame oil

Agricultural by-products of sesame are promising bioresources in food processing. This study extracted lignin from the by-products of sesame oil production, namely, the capsules and straw of black and white sesame. Using acid, alkali, and ethanol methods, 12 distinct lignins were obtained to prepare biochar, aiming to investigate both the structural characteristics of lignin-based biochar (LBB) and its ability to remove benzo[a]pyrene (BaP) from sesame oil. The results showed that white sesame straw was the most suitable raw material for preparing biochar. In terms of the preparation method, acid-extracted lignin biochar was more effective in removing BaP than alkaline or ethanol methods. Notably, WS-1LB (white sesame straw acid-extracted lignin biochar) exhibited the highest BaP adsorption efficiency (91.44 %) and the maximum specific surface area (1065.8187 m2/g), characterized by porous structures. The pseudo 2nd and Freundlich models were found to be the best fit for the adsorption kinetics and isotherms of BaP on LBB, respectively, suggesting that a multilayer adsorption process was dominant. The high adsorption of LBB mainly resulted from pore filling. This study provides an economical and highly efficient biochar adsorbent for the removal of BaP in oil.

Biochar with enhanced performance prepared based on “graphite-structure regulation” conjecture designed to effectively control water pollution

In this work, corn straw was used as raw material, Hummers method and activation were used to adjust the graphite structure in biochar, and preparing straw based biochar (H-BCS) with ultra-high specific surface area (3441.80 m2/g), highly total pore volume (1.9859 cm3/g), and further enhanced physicochemical properties. Compared with untreated straw biochar (BCS), the specific surface area and total pore volume of H-BCS were increased by 47.24 % and 55.85 %, respectively. H-BCS showed good removal ability in subsequent experiments by using chloramphenicol (CP), hexavalent chromium (Cr6+), and crystal violet (CV) as adsorption models. In addition, the adsorption capacities of H-BCS (CP: 1396.30 mg/g, Cr6+: 218.40 mg/g, and CV: 1246.24 mg/g) are not only higher than most adsorbents, even after undergoing 5 cycles of regeneration, its adsorption capacity remains above 80 %, indicating significant potential for practical applications. In addition, we also speculated and analyzed the conjecture about the “graphite-structure regulation” during the preparation process, and finally discussed the possible mechanism during the adsorption processes. We hope this work could provide a new strategy to solve the restriction of biochar performance by further exploring the regulation of graphite structure in carbon materials.

Synergistic interactions between lignite and biomass during co-pyrolysis from volatile release, kinetics, and char structure

One of the most efficient techniques to achieve efficient utilization of both is coal and biomass co-pyrolysis. Despite a great deal of recent research on the co-pyrolysis process, it is still unknown how biomass affects the co-pyrolysis's synergistic effect and how volatiles interact. This study uses a thermogravimetric analyzer to examine the weight loss law of co-pyrolysis of wheat straw, rice straw, and bamboo powder with various amounts of Zhundong coal. According to the findings, there is a strong positive interaction, a mild positive interaction, and a negative interaction when three different types of biomass (wheat straw, rice straw, bamboo straw) are co-pyrolysis with Zhundong coal. The interaction between wheat straw and Zhundong coal is the strongest when the mass ratio of wheat straw to Zhundong coal is 6: 4. Using a thermogravimetric-infrared spectrometer, the changes in volatile functional groups during co-pyrolysis are investigated. It is discovered that adding wheat straw decreased the amount of CO2 produced by Zhundong coal pyrolysis. Regarding the mechanism of co-pyrolysis, the alkali and alkaline earth metals (AAEMs) on the surface of biochar catalyze the pyrolysis of Zhundong coal, while the “hydrogen donor” and “free radical donor” generated by biomass pyrolysis inhibited the cross-linking and polymerization of macromolecular volatiles produced by Zhundong coal pyrolysis. The activation energy of the mass ratio of wheat straw to Zhundong coal = 6: 4 sample is calculated by three model-free methods. The co-pyrolysis process's average activation energy is determined to be between 175.95 and 194.18 kJ/mol. Through scanning electron microscopy, it is found that the morphology of co-pyrolysis carbon is significantly different from that of single pyrolysis carbon. The porous structure of biochar promotes the secondary cracking of heavy volatiles produced by coal pyrolysis, while the cracking of volatiles further promotes the development of the pore structure of biochar.

Coupling machine learning and theoretical models to compare key properties of biochar in adsorption kinetics rate and maximum adsorption capacity for emerging contaminants

Insights into key properties of biochar with a fast adsorption rate and high adsorption capacity are urgent to design biochar as an adsorbent in pollution emergency treatment. Machine learning (ML) incorporating classical theoretical adsorption models was applied to build prediction models for adsorption kinetics rate (i.e., K) and maximum adsorption capacity (i.e., Qm) of emerging contaminants (ECs) on biochar. Results demonstrated that the prediction performance of adaptive boosting algorithm significantly improved after data preprocessing (i.e., log-transformation) in the small unbalanced datasets with R2 of 0.865 and 0.874 for K and Qm, respectively. The surface chemistry, primarily led by ash content of biochar significantly influenced the K, while surface porous structure of biochar showed a dominant role in predicting Qm. An interactive platform was deployed for relevant scientists to predict K and Qm of new biochar for ECs. The research provided practical references for future engineered biochar design for ECs removal.