ISSN 1000-3665 CN 11-2202/P

    某场地不同深度土壤中铬分布特征及主控因子研究

    Distribution characteristic of chromium in soil at different depths and main control factors of a contaminated site

    • 摘要: 铬渣渗漏液中富含Cr(Ⅵ),毒性大且迁移性强,对生态环境危害严重。目前,针对铬渣类污染场地中多个含水层和隔水层Cr污染的研究较少,且影响Cr迁移转化的主控因子也尚不清晰,为探究此类条件下Cr的迁移转化规律,文章以某铬渣场地为例,通过土壤样品采集与分析,利用数理统计、克里格插值和因子分析等方法查明不同深度土壤中Cr的分布特征,识别污染和未污染土壤中Cr的不同形态及占比,并探讨介质中铁、铝含量等因子对Cr在土壤中迁移转化的影响。结果表明:(1)场地及周边距地表40 m以浅的土壤受到不同程度的Cr污染,且Cr(Ⅵ)质量分数在粉质黏土、黏土中高于砂性介质;(2)不同深度土壤中弱酸态Cr占比小于10%,未污染土壤中残渣态Cr占比37%~63%,而污染土壤中Cr主要以可还原态形式存在,可交换态和可还原态Cr构成该场地Cr迁移转化的主要形式;(3)不同深度土壤中铁、铝含量呈线性关系,铁、铝含量增大可提升土壤对Cr(Ⅵ)的吸附能力,其效果在粉质黏土、黏土层中更为显著;(4)阳离子交换能力增大有利于促进土壤对Cr(Ⅲ)的吸附,锰氧化物通过吸附、氧化反应和微生物作用促进Cr(Ⅲ)向Cr(Ⅵ)转化,而有机质通过吸附、还原反应和微生物作用驱动Cr(Ⅵ)向Cr(Ⅲ)转化,土壤pH值既能通过改变颗粒表面电荷量影响Cr(Ⅲ) 和Cr(Ⅵ)的吸附量,又能同阳离子交换能力共同促进Cr(Ⅲ)的吸附,与有机质协同影响Cr(Ⅵ)的吸附。因此,准确识别场地水文地质条件对分析Cr在土壤中的迁移转化至关重要,研究成果可为铬渣类污染场地的风险管控与后期修复提供有力支撑。

       

      Abstract: Chromium slag leachate is rich in Cr(Ⅵ), which is highly toxic and migratory, posing serious harm to the ecological environment. There are fewer studies involving multiple aquifers and aquitards contaminated with chromium, and the main controlling factors affecting chromium migration and transformation are not yet clear. In order to investigate the migration and transformation patterns of chromium in soil under such condition, a chromium contaminated site was taken as an example in this study, the spatial distribution of Cr in soil at different depths, the different forms and proportions of Cr in uncontaminated and contaminated soils, and the factors such as iron and aluminum content in soil affecting the migration and transformation of Cr were analyzed by sampling and testing soil samples, and the combination using of methods such as mathematical statistics, Kriging interpolation and factor analysis. The results shown that (1) Soil below ground surface 40 m was polluted by Cr with different degrees around the chromium slag heap, and the percentage of Cr(VI) mass fraction was higher in clay or silt caly than in sand layer. (2) The proportion of Cr in weak acidic state in soil at different depths was less than 10%, and the proportion of Cr in residual state ranged from 37% to 63% in uncontaminated soil, but it mainly existed in the form of reducible state in contaminated soil. The exchangeable and reducible states of Cr were the main forms of Cr migration and transformation at this site. (3) There was a linear relationship between the Fe and Al content in soil at different depths, and the increase of Fe and Al content could enhance the adsorption capacity of soil for Cr(Ⅵ), especially in the silty clay and clay layers. (4) Increased cation exchange capacity (CEC) promoted the adsorption of Cr(Ⅲ) in soil at different depths. Manganese oxides favored the conversion of Cr(Ⅲ) to Cr(VI) through adsorption, oxidation reaction and microbial action, while organic matter drived the conversion of Cr(VI) to Cr(Ⅲ) through adsorption, reduction reaction and microbial action. Soil pH affected the adsorption of Cr(Ⅲ) and Cr(VI) by changing the surface charge of particle, and also promoted the adsorption of Cr(Ⅲ) together with CEC, or affected the adsorption of Cr(VI) with organic matter. Therefore, accurate identification of site hydrogeological condition is essential for analyzing the transformation of Cr in soil. The results of this research can provide strong support for risk management and post remediation of chromium slag contaminated sites.

       

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