Performance and mechanism of biochar@FeMg-LDH for efficient activation of persulfate for degradation of 2, 4-dichlorophenol in groundwater.

Groundwater environments are complex, and traditional advanced oxidation technologies mainly based on free radicals have limitations such as poor selectivity and low interference resistance, making it difficult to efficiently degrade target pollutants in groundwater. Therefore, we developed a sludge-based biochar-supported FeMg-layered double hydroxide catalyst (BC@FeMg-LDH) for the catalytic degradation of 2, 4-dichlorophenol (2, 4-DCP) using persulfate (PDS) as an oxidant. The removal efficiency of the catalyst exceeded 95%, showing high oxidation activity in a wide pH range while being almost unaffected by reducing substances and ions in the environment. Meanwhile, under neutral conditions, the leaching of metal ions from BC@FeMg-LDH was minimal, thereby eliminating the risk of secondary pollution. According to quenching experiments and electron paramagnetic resonance spectroscopy, the main active species during BC@FeMg-LDH/PDS degradation of 2, 4-DCP is 1O2, indicating a non-radical reaction mechanism dominated by 1O2. Characterization techniques, including X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy, revealed that the carbonyl (C = O) and metal hydroxyl (M-OH) groups on the material surface were the main reactive sites mediating 1O2 generation. The 1O2 generation mechanism during the reaction involved ketone-like activation of carbonyl groups on the biochar surface and complexation of hydroxyl groups on the material surface with PDS, resulting in the formation of O2·- and further generation of 1O2. 1O2 exhibited high selectivity toward electron-rich organic compounds such as 2, 4-DCP and demonstrated strong interference resistance in complex groundwater environments. Therefore, BC@FeMg-LDH holds promising applications for the remediation of organic-contaminated groundwater.

Efficient adsorption of Cu2+ and Cd2+ from groundwater by MgO-modified sludge biochar in single and binary systems.

In this study, MgO-modified sludge biochar (1MBC) prepared from sewage sludge was successfully used as an efficient adsorbent to remove heavy metals from groundwater. The adsorption performance and mechanism of 1MBC on Cu2+ and Cd2+ were investigated in single and binary systems, and the contribution of different mechanisms was quantified. Adsorption kinetics and isotherms analysis revealed that the adsorption processes of Cu2+ and Cd2+ by 1MBC followed the pseudo-second-order kinetic and Langmuir isotherm model in both systems, indicating that Cu2+ and Cd2+ were mainly controlled by chemisorption, and their theoretical maximum adsorption capacities were 240.36 and 219.06 mg·g-1, respectively. The results of the binary system showed that due to the competitive adsorption, the adsorption capacity of 1MBC for both heavy metals was lower than that of the single system, and the selective adsorption of Cu2+ was higher. The influencing variable experiments revealed that the adsorption of Cu2+ and Cd2+ by 1MBC had a wide pH adaption range and strong anti-interference ability to coexisting organics and ions. The adsorption mechanisms involved ion exchange (Cu: 47.39%, Cd: 53.17%), mineral precipitation (Cu: 35.31%, Cd: 24.18%), functional group complexation (Cu: 10.44%, Cd: 14.53%), and other possible mechanisms (Cu: 6.87%, Cd: 8.12%). Furthermore, 1MBC demonstrated excellent regeneration potential after five cycle times. Overall, the results have significant reference value for the practical application of removing heavy metals.