Given that the problem of contaminated soil continues to grow, the development of effective control and remediation measures has become imperative, especially for heavy-metal-contaminated soil. Biochar and modified biochar are eco-friendly and cost-effective remediation materials that are widely used in the remediation of contaminated soil. This review provides an overview of the different raw materials used in the preparation of biochar as well as the modification of biochar using various synthesis methods, highlighting their differences and providing recommendations for biochar and modified biochar as applied toward ameliorating pollution in soil contaminated by heavy metals. We also explore the effects of the physicochemical properties of raw materials, pyrolysis temperature, additives, and modification methods on the properties of the resulting biochar and modified biochar, and systematically present the types of soil and operating factors for repair. Moreover, the mechanisms involved in remediation of heavy-metal-contaminated soil by biochar and modified biochar are outlined in detail, and include adsorption, complexation, precipitation, ion exchange, and electrostatic attractions. Finally, the corresponding monitoring technologies after remediation are illustrated. Future directions for studies on biochar and modified biochar in the remediation of contaminated soil are also proposed to support the development of green environmental protection materials, simple preparation methods, and effective follow-up monitoring techniques.

The interaction between Ca-HAP and Pb2+ solution can result in the formation of a hydroxyapatite–hydroxypyromorphite solid solution [(PbxCa1−x)5(PO4)3(OH)], which can greatly affect the transport and distribution of toxic Pb in water, rock and soil. Therefore, it’s necessary to know the physicochemical properties of (PbxCa1−x)5(PO4)3(OH), predominantly its thermodynamic solubility and stability in aqueous solution. Nevertheless, no experiment on the dissolution and related thermodynamic data has been reported. Dissolution of the hydroxypyromorphite–hydroxyapatite solid solution [(PbxCa1−x)5(PO4)3(OH)] in aqueous solution at 25 °C was experimentally studied. The aqueous concentrations were greatly affected by the Pb/(Pb + Ca) molar ratios (XPb) of the solids. For the solids with high XPb [(Pb0.89Ca0.11)5(PO4)3OH], the aqueous Pb2+ concentrations increased rapidly with time and reached a peak value after 240–720 h dissolution, and then decreased gradually and reached a stable state after 5040 h dissolution. For the solids with low XPb (0.00–0.80), the aqueous Pb2+ concentrations increased quickly with time and reached a peak value after 1–12 h dissolution, and then decreased gradually and attained a stable state after 720–2160 h dissolution. The dissolution process of the solids with high XPb (0.89–1.00) was different from that of the solids with low XPb (0.00–0.80). The average K sp values were estimated to be 10−80.77±0.20 (10−80.57–10−80.96) for hydroxypyromorphite [Pb5(PO4)3OH] and 10−58.38±0.07 (10−58.31–10−58.46) for calcium hydroxyapatite [Ca5(PO4)3OH]. The Gibbs free energies of formation (ΔG ) were determined to be −3796.71 and −6314.63 kJ/mol, respectively. The solubility decreased with the increasing Pb/(Pb + Ca) molar ratios (XPb) of (PbxCa1‒x)5(PO4)3(OH). For the dissolution at 25 °C with an initial pH of 2.00, the experimental data plotted on the Lippmann diagram showed that the solid solution (PbxCa1−x)5(PO4)3(OH) dissolved stoichiometrically at the early stage of dissolution and moved gradually up to the Lippmann solutus curve and the saturation curve for Pb5(PO4)3OH, and then the data points moved along the Lippmann solutus curve from right to left. The Pb-rich (PbxCa1−x)5(PO4)3(OH) was in equilibrium with the Ca-rich aqueous solution.

This study details the preparation of Fe-Mn binary oxide/mulberry stem biochar composite adsorbent (FM-MBC) from mulberry stems via the multiple activation by potassium permanganate, ferrous chloride, triethylenetetramine, and epichlorohydrin. The characteristics of FM-MBC had been characterized by SEM-EDS, BET, FT-IR, XRD, and XPS, and static adsorption batch experiments such as pH, adsorption time, were carried out to study the mechanism of Cr(VI) adsorption on FM-MBC and the impact factors. The results indicated that in contrast with the mulberry stem biochar (MBC), the FM-MBC has more porous on surface with a BET surface area of 74.73 m²/g, and the surface loaded with α-Fe₂O₃ and amorphization of MnO₂ particles. Besides, carboxylic acid, hydroxyl, and carbonyls functional groups were also formed on the FM-MBC surface. At the optimal pH 2.0, the maximum adsorption capacity for Cr(VI) was calculated from the Langmuir model of 28.31, 31.02, and 37.14 mg/g at 25, 35, and 45 °C, respectively. The aromatic groups, carboxyls, and the hydroxyl groups were the mainly functional groups in the adsorption of Cr(VI). The mechanism of the adsorption process of FM-MBC for Cr(VI) mainly involves electrostatic interaction, surface adsorption of Cr(VI) on FM-MBC, and ion exchange.

Noble metal materials have been identified as high efficiency catalysts for electrocatalytic reduction of nitrate, and the synthesis and manufacture of high catalytic activity and environmentally friendly catalysts of activating hydrogen for water purification applications is extremely attractive. In this work, the Pd–Cu single-atom catalysts (Pd–Cu-N-BC) were first prepared by direct growth of Pd–Cu single-atom on bamboo biochar by regulating the concentration of precursors and doping method, and then enhanced electrocatalytic reduction nitrate performance and N₂ generation. The results showed that Pd–Cu-N-BC displayed excellent catalytic activity and reusability in electrocatalytic reduction nitrate with a low potential of 0.47 V vs. RHE (@10 mA cm⁻²). The maximum nitrate removal efficiency and N₂ generation could reach about 100% and 72.32% within 180 min, respectively. The density functional theory (DFT) calculations confirmed that Cu atoms could catalyze the electrochemical reduction of nitrate to nitrite, and Pd atoms anchored in the nitrogen-doped biochar (N-BC) lattice could catalyze electrochemical reduction of nitrite to N₂ involving the formation of hydrogen radical (H*). The characterization results of XANES showed that electronic synergistic effect between Pd and Cu single atoms significantly promotes the N₂ production through hydrogenation while inhibiting the generation of byproducts, leading to significantly enhanced electrocatalytic reduction of nitrate to N₂. Finally, Pd–Cu-N-BC was designed as a 3D particle electrode for enhanced electrocatalytic reduction of nitrate, exhibiting excellent stability and reusability, which could be considered as a suitable candidate for applications in the remediation of nitrate contamination. Graphical Abstract

A novel material named Fe/Mn-C layered double hydroxide composite (Fe/Mn-C-LDH) was synthesized to remove arsenic from an aqueous solution. The removal performance of the composite toward arsenic ions was studied through the batch experiments. The experiment results showed that Fe/Mn-C-LDH exhibited a high adsorption capacity of 46.47 mg/g for As(III) and 37.84 mg/g for As(V) at 318 K, respectively. In addition, the investigation of the release of Fe³⁺ and Mn²⁺ in the process of arsenic adsorption revealed that the Fe/Mn-C-LDH exhibited better stability than Fe/Mn-layer double hydroxide (Fe/Mn-LDH) with fewer Mn²⁺ and Fe³⁺ releasing under the same condition. The BET results showed that the specific surface area of Fe/Mn-C-LDH decreased after adsorption of As (III) and As (V). Furthermore, the Density Functional Theory (DFT) calculation results proved that the adsorbent combining arsenic by T-site to produce a better adsorption effect for arsenic. Possessing better stability and adsorption capacity, Fe/Mn-C-LDH could potentially serve as a perfect adsorbent for arsenic removal from an aqueous environment. It would provide a promising approach for removing heavy metal from the aquatic environment in the future.