异位化学还原修复铬污染场地的生命周期碳排放特征与优化策略

Life cycle carbon emission characteristics and optimization strategies for ex-situ chemical reduction remediation of a chromium-contaminated site

  • 摘要: 场地修复是削减土壤环境污染和降低健康风险的重要技术手段,但修复过程通常伴随着高强度能源消耗与药剂使用,从而引发碳排放等额外的环境负担。以华东地区某铬污染场地为例,从生命周期视角分析异位化学还原修复工程的碳排放特征及环境影响。结果表明,修复1 m3污染土壤的终点环境影响为728.12 Pt,基于IPCC碳排放因子法核算的碳排放水平为0.244 0 t(以CO2当量计)。化学还原是碳排放和环境影响的主导环节,贡献率分别为86.63%和69.88%。不确定性与敏感性分析结果显示,碳排放核算结果不确定性相对较低,变异系数为5.25%。铁粉、生石灰和硫酸亚铁消耗量为敏感参数,是影响碳排放水平的关键。基于生命周期评价与碳排放核算结果,研究提出了异位化学还原修复的优化策略,包括基于浓度分区的精准修复、工业副产物类药剂的低碳替代,以及基于氧化还原电位实时监测的动态调控,以期为污染场地绿色低碳修复提供理论依据。

     

    Abstract: Site remediation plays a vital role in reducing soil contamination and mitigating associated human health risks. However, remediation activities are typically accompanied by intensive energy consumption and substantial reagent inputs, which in turn generate additional environmental burdens such as carbon emissions. Taking a chromium-contaminated site in East China as a case study, this study analyzed the carbon emission characteristics and environmental impacts of the ex-situ chemical reduction remediation project from a life cycle perspective. The results indicated that the endpoint environmental impact of remediating 1 m3 of contaminated soil was 728.12 Pt, while the carbon emissions calculated by the IPCC emission factor method amounted to 0.244 0 t CO2-equivalent. The chemical reduction was the dominant contributor to both carbon emissions and environmental impacts, accounting for 86.63% and 69.88%, respectively. Uncertainty and sensitivity analyses demonstrated relatively low uncertainty in carbon emission estimates, with a coefficient of variation of 5.25%. The consumption of iron powder, quicklime, and ferrous sulfate were identified as sensitive parameters and key determinants of carbon emission levels. Building on the results of life cycle assessment and carbon emission accounting, targeted optimization strategies for ex-situ chemical reduction remediation were proposed, focusing on concentration-based zonation for refined remediation, low-carbon substitution for industrial by-product based chemicals, and dynamic regulation based on real-time monitoring of oxidation–reduction potential, to provide theoretical support for the development of green and low-carbon remediation practices for contaminated sites.

     

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