生物炭
化学
激进的
过氧化氢
电子顺磁共振
羟基自由基
光化学
甲苯
降级(电信)
热解
自旋俘获
有机化学
计算机科学
核磁共振
电信
物理
作者
Guodong Fang,Juan Gao,Cun Liu,Dionysios D. Dionysiou,Yujun Wang,Dongmei Zhou
摘要
We investigated the activation of hydrogen peroxide (H2O2) by biochars (produced from pine needles, wheat, and maize straw) for 2-chlorobiphenyl (2-CB) degradation in the present study. It was found that H2O2 can be effectively activated by biochar, which produces hydroxyl radical (•OH) to degrade 2-CB. Furthermore, the activation mechanism was elucidated by electron paramagnetic resonance (EPR) and salicylic acid (SA) trapping techniques. The results showed that biochar contains persistent free radicals (PFRs), typically ∼1018 unpaired spins/gram. Higher trapped [•OH] concentrations were observed with larger decreases in PFRs concentration, when H2O2 was added to biochar, indicating that PFRs were the main contributor to the formation of •OH. This hypothesis was supported by the linear correlations between PFRs concentration and trapped [•OH], as well as kobs of 2-CB degradation. The correlation coefficients (R2) were 0.723 and 0.668 for PFRs concentration vs trapped [•OH], and PFRs concentration vs kobs, respectively, when all biochars pyrolyzed at different temperatures were included. For the same biochar washed by different organic solvents (methanol, hexane, dichloromethane, and toluene), the correlation coefficients markedly increased to 0.818–0.907. Single-electron transfer from PFRs to H2O2 was a possible mechanism for H2O2 activation by biochars, which was supported by free radical quenching studies. The findings of this study provide a new pathway for biochar implication and insight into the mechanism of H2O2 activation by carbonaceous materials (e.g., activated carbon and graphite).
科研通智能强力驱动
Strongly Powered by AbleSci AI