School of Environment, Nanjing Normal University, Nanjing, Jiangsu province, 210023, China.
National-Regional Joint Engineering Research Center for Soil Pollution Control and Remediation in South China, Guangdong Key Laboratory of Integrated Agro-environmental Pollution Control and Management, Institute of Eco-environmental and Soil Sciences, Guangdong Academy of Sciences, Guangzhou, Guangdong province, 510650, China.
J Environ Manage. 2024 Apr;356:120457. doi: 10.1016/j.jenvman.2024.120457. Epub 2024 Mar 19.
Ferrous sulfate (FeSO) combined with acid pretreatment is usually employed to remediate contaminated soils containing Cr(VI). However, the long-term efficiency of this stabilization method is important for its sustainability. In this study, a gradient temperature-elevating exposure test was employed to investigate the stability of Cr in FeSO-remediated soil when exposed to elevated temperatures (40 °C, 120 °C, and 500 °C), possibly caused by hot weather and/or wildfires. The results of chemical extraction and X-ray absorption near edge structure spectroscopy (XANES) showed that the Cr(VI) in contaminated soil was successfully transformed to Cr(III) after stabilization, resulting in the dramatic decrease of water-leachable Cr(VI). The stabilization efficiency was further improved under 40 °C treatment after 30 days. Subsequently, the 120 °C treatment (7 days) had relatively little effect on the Cr speciation and mobility in soils. However, even one day of 500 °C calcination resulted in the deterioration of stabilization efficiency, and the water-leachable Cr(VI) re-increased and became higher than the Chinese environmental standards (total Cr 15 mg/L, Cr(VI) 5 mg/L) for the classification of hazardous solid wastes. XANES results reflected that heating at 500 °C facilitate the formation of CrO, which was mainly caused by thermal decomposition and dehydration of Cr(OH) in the soil. Besides, the transformation of Cr species resulted in the enhanced association of Cr with the most stable residual fraction (88.3%-91.6%) in soil. Based on chemical extraction results, it was suggested that the oxidation of Cr(III) to Cr(VI) contributed to the re-increased mobility of Cr(VI) in soil. However, the XANES results showed that almost no significant re-oxidization of Cr(III) to Cr(VI) happened after heating at 500 °C, which was probably caused by XANES linear combination fits (LCF) uncertainties. Moreover, the changes in soil properties, including a rise in pH to a slightly alkaline range and/or the decomposition of organic matter, possibly contributed to the enhanced mobility of Cr(VI) in soil. This study contributes to clarifying the mobility and transformation of Cr in contaminated soils and provides a support for the sustainable management of remediated soils.
硫酸亚铁(FeSO)结合酸预处理通常用于修复含有 Cr(VI)的污染土壤。然而,这种稳定化方法的长期效率对于其可持续性很重要。在本研究中,采用梯度升温暴露试验研究了在可能由炎热天气和/或野火引起的高温(40°C、120°C 和 500°C)下,FeSO 修复土壤中 Cr 的稳定性。化学提取和 X 射线吸收近边结构光谱(XANES)的结果表明,污染土壤中的 Cr(VI)在稳定化后成功转化为 Cr(III),导致水溶态 Cr(VI)急剧下降。在 30 天后进行 40°C 处理,稳定效率进一步提高。随后,120°C 处理(7 天)对土壤中 Cr 形态和迁移性的影响相对较小。然而,即使是 500°C 煅烧一天也会导致稳定效率恶化,水溶态 Cr(VI)再次增加,超过中国危险废物分类标准(总 Cr 15mg/L,Cr(VI) 5mg/L)。XANES 结果表明,在 500°C 加热条件下促进了 CrO 的形成,这主要是由于土壤中 Cr(OH)的热分解和脱水作用。此外,Cr 物种的转化导致 Cr 与土壤中最稳定的残留部分(88.3%-91.6%)的结合增强。基于化学提取结果,建议 Cr(III)氧化为 Cr(VI)导致 Cr(VI)在土壤中的迁移性增加。然而,XANES 结果表明,在 500°C 加热后,Cr(III)几乎没有明显地重新氧化为 Cr(VI),这可能是由于 XANES 线性组合拟合(LCF)的不确定性所致。此外,土壤性质的变化,包括 pH 升高到略碱性范围和/或有机质分解,可能导致 Cr(VI)在土壤中的迁移性增强。本研究有助于阐明污染土壤中 Cr 的迁移和转化,为修复土壤的可持续管理提供支持。