Key Laboratory of Soil Environment and Pollution Remediation, Institute of Soil Science, Chinese Academy of Sciences, Nanjing 210008, China; University of Chinese Academy of Sciences, Beijing 100049, China; Jiangsu Engineering Laboratory for Soil and Groundwater Remediation of Contaminated Sites, Institute of Soil Science, Chinese Academy of Sciences, Nanjing 210008, China.
Key Laboratory of Soil Environment and Pollution Remediation, Institute of Soil Science, Chinese Academy of Sciences, Nanjing 210008, China; Jiangsu Engineering Laboratory for Soil and Groundwater Remediation of Contaminated Sites, Institute of Soil Science, Chinese Academy of Sciences, Nanjing 210008, China.
Sci Total Environ. 2022 Jul 10;829:154645. doi: 10.1016/j.scitotenv.2022.154645. Epub 2022 Mar 17.
A facile, green and easily-scalable method of synthesizing stable and effective nano zero-valent iron (nZVI)‑carbon composites for peroxymonosulfate (PMS) activation was highly desirable for in-situ groundwater remediation. This study developed a two-step hydrothermally assisted carbothermal reduction method to prepare nZVI-encapsulated carbon composite (Fe@C) using rice straw and ferric nitrate as precursors. The hydrothermal reactions were conducive to iron loading, and carbothermal temperature was crucial for the aromatization and graphitization of hydrothermal carbonaceous products, the reductive transformation of iron oxides into nZVI and the development of porous structure in composites. At carbothermal temperature of 800 °C following hydrothermal reactions, the stable Fe@C800 with nZVI encapsulated in the spherical carbon shell was obtained and exhibited the best catalytic performance for PMS activation and the degradation of monochlorobenzene (MCB) in a wide range of pH values (3-11) with removal efficiency after 120 min reaction and first-order kinetic rate constant (k) of 98.7% and 0.087 min respectively under the optimum conditions of 10 mM PMS and 0.2 g·L Fe@C800. The inhibiting effects of common co-existed anions (i.e., Cl, HCO and HPO) and humic acid in groundwater on the removal of MCB in Fe@C800/PMS system was also investigated. Both OH-dominated radical processes and nonradical pathways involving O and surface electron transfers were accounted for PMS activation and MCB removal. The inner nZVI was protected by the carbon shell, endowing Fe@C800 with high reactivity and good reusability. Additionally, 81.2% and 73.5% of MCB removal rates were achieved in tap water and actual contaminated groundwater respectively. This study not only provided a novel strategy to synthesize highly effective and stable nZVI‑carbon composites using the agricultural biomass waste for PMS induced oxidation of organic contaminants in groundwater, but also enhanced the understanding on the activation mechanism of iron‑carbon based catalysts towards PMS.
一种简便、绿色且易于规模化的方法,用于合成稳定且有效的纳米零价铁(nZVI)-碳复合材料,以用于过一硫酸盐(PMS)的激活,这对于原位地下水修复非常理想。本研究采用稻草和硝酸铁作为前体,开发了一种两步水热辅助碳热还原法制备 nZVI 封装碳复合材料(Fe@C)。水热反应有利于铁的负载,而碳热温度对于水热碳质产物的芳构化和石墨化、铁氧化物还原转化为 nZVI 以及复合材料中多孔结构的发展至关重要。在水热反应后进行碳热处理,温度为 800°C,得到了稳定的 Fe@C800,其中 nZVI 封装在球形碳壳中,在广泛的 pH 值(3-11)范围内对 PMS 激活和单氯苯(MCB)的降解表现出最佳的催化性能,在最佳条件下,120 min 反应后的去除效率和一级动力学速率常数(k)分别为 98.7%和 0.087 min,在 10 mM PMS 和 0.2 g·L Fe@C800 下。还研究了常见共存阴离子(即 Cl、HCO 和 HPO)和地下水腐殖酸对 Fe@C800/PMS 体系中 MCB 去除的抑制作用。PMS 激活和 MCB 去除涉及 OH 主导的自由基过程和涉及 O 和表面电子转移的非自由基途径。内部分布的 nZVI 被碳壳保护,赋予 Fe@C800 高反应性和良好的可重复使用性。此外,在自来水和实际受污染的地下水中,MCB 的去除率分别达到 81.2%和 73.5%。本研究不仅提供了一种使用农业生物质废物合成高效稳定的 nZVI-碳复合材料的新策略,用于地下水有机污染物的过一硫酸盐诱导氧化,而且还增强了对铁-碳基催化剂对 PMS 激活机制的理解。