生态环境学报 ›› 2026, Vol. 35 ›› Issue (7): 997-1004.DOI: 10.16258/j.cnki.1674-5906.2026.07.001

• “新污染物”研究专栏 •    下一篇

过渡金属改性有机蒙脱石对四溴双酚A污染土壤修复作用研究

花莉*(), 陈雨, 代高凡, 李琳丰   

  1. 陕西科技大学环境科学与工程学院陕西 西安 710021
  • 收稿日期:2025-10-29 修回日期:2026-01-10 接受日期:2026-03-09 出版日期:2026-07-18 发布日期:2026-07-17
  • 通讯作者: *花莉, huali@sust.edu.cn
  • 作者简介:花莉(1979年生),女,教授,博士,博士研究生导师,研究方向为污染环境生态技术研发;生物质炭的环境效益研究(温室气体减排及土壤碳截留)。E-mail: huali@sust.edu.cn
  • 基金资助:
    国家自然科学基金项目(22376133);陕西省重点研发计划项目(2024PT-ZCK-09)

Iron-modified Organo-montmorillonite Nanocomposites for Enhanced Remediation of Tetrabromobisphenol A Contaminated Soil

Hua Li*(), Chen Yu, Dai Gaofan, Li Linfeng   

  1. College of Environmental Science and Technology, Shaanxi University of Science and Technology, Xi’an 710021, P. R. China
  • Received:2025-10-29 Revised:2026-01-10 Accepted:2026-03-09 Online:2026-07-18 Published:2026-07-17

摘要:

为实现四溴双酚A(TBBPA)污染土壤的有效修复与治理,制备多种蒙脱石基过渡金属材料,经对比筛选后确定以零价纳米铁改性有机蒙脱石(nZVI@CMT)为目标修复材料。借助SEM、TEM、XRD、FTIR及XPS对材料进行了表征,分析其改性前后的形态与结构变化;通过测定土壤中TBBPA浓度变化、土壤酶活性及生物形态等指标,系统评价nZVI@CMT对TBBPA污染土壤的修复效果;采用LC-MS联用技术监测nZVI@CMT去除土壤TBBPA过程中可能产生的反应产物,探讨了其反应途径。结果表明:在自然环境条件下,未添加nZVI@CMT的污染组土壤,42 d后TBBPA去除率仅为19.90%;而添加nZVI@CMT的处理组土壤,42 d时TBBPA去除率提升至73.15%。同时,nZVI@CMT对土壤酶活性具有正向调节作用,可有效减缓TBBPA对土壤中蚯蚓的损伤,改善污染土壤中种子的发芽率及发芽趋势,对TBBPA污染土壤展现出良好的修复效能。此外,LC-MS分析证实,TBBPA在土壤中的主要降解过程包括β键断裂、去甲基化及苯环开环反应。该研究以有机-无机复合改性制备ZVI@CMT,用于TBBPA污染土壤修复,结合土壤理化、酶活性及生物指标评价,为污染土壤可持续修复提供全面依据。

关键词: 蒙脱石, 有机改性, 零价纳米铁, 四溴双酚A, 土壤修复

Abstract:

Tetrabromobisphenol A (TBBPA) is one of the most widely used brominated flame retardants (BFRs). It is predominantly used as a reactive additive in the fabrication of printed circuit boards and finds extensive applications in industries such as the electronics, electrical appliances, plastics, textiles, and building materials. Owing to its lipophilic nature, TBBPA tends to accumulate persistently in soil. Long-term accumulation in soil poses potential risks to human health through food chain transmission, thus rendering the remediation of TBBPA-contaminated soil an issue of critical importance. Current methods for TBBPA removal include physical, biological, and chemical technologies, yet each suffers from inherent limitations: Physical methods are often constrained by low adsorption and degradation efficiency, while biological and chemical technologies are constrained by their stringent reaction conditions, hindering large-scale industrial application. Against this backdrop, the integration of multiple treatment technologies has emerged as a major research focus. Montmorillonite (MT), owing to its layered structure and expandable interlayers, is commonly exploited as an adsorbent or catalyst support in environmental remediation. Nanoscale transition metals are widely utilized as catalytic active sites in various catalytic systems, such as Advanced Oxidation Processes (AOPs). When immobilized on catalyst surfaces, nanoscale transition metals can generate hydroxyl radicals to degrade pollutants; however, their poor dispersibility often impedes degradation efficiency. The multilayered structure of MT not only serves as an ideal carrier for nanoscale transition metals but also, as studies have shown, organically modified MT can effectively enhance the dispersion of these metals, thereby improving their pollutant degradation efficiency. To achieve efficient remediation of TBBPA-contaminated soil, this study prepared a series of MT-based materials. By comparing the TBBPA removal efficiencies of different materials, the optimal target remediation material was screened. Initially, organically modified montmorillonite (CMT) was synthesized via an ion exchange method. Subsequently, several materials were prepared, including zero-valent iron nanoparticle-modified organomontmorillonite (nZVI@CMT). The TBBPA removal rate was adopted as the primary indicator to evaluate the performance of both pristine and unmodified MT materials. High-performance liquid chromatography (HPLC) was used to determine TBBPA concentrations. Moreover, soil enzyme activity assays, earthworm epidermal damage tests, and seed germination experiments were conducted to comprehensively assess the ecological remediation efficacy of nZVI@CMT on TBBPA-contaminated soil. Results from comparative studies demonstrated that nZVI@CMT exhibited the best TBBPA removal performance, achieving a removal rate of 98.28% within 60 minutes. Accordingly, nZVI@CMT was identified as the target remediation material. The material was characterized using SEM, TEM, XRD, FTIR, and XPS to analyze morphological and structural changes before and after modification. SEM images revealed that zero-valent iron nanoparticles were uniformly distributed on the montmorillonite surface in a granular form, effectively mitigating their agglomeration tendency. TEM results further corroborated these observations. XRD analysis indicated that the structure of the modified nano-zero-valent iron montmorillonite was similar to that of unmodified montmorillonite, confirming that the layered molecular structure remained largely unchanged after organic modification and nZVI loading. However, a significant increase in the interlayer spacing after organic modification confirmed the intercalation of modifiers into the montmorillonite layers. The diffraction peaks of zero-valent iron also verified the successful immobilization of nZVI on CMT. XPS and FTIR were employed to investigate changes in elemental valence states and functional groups. The XPS spectrum of nZVI@CMT exhibited distinct Fe2p characteristic peaks. FTIR analysis showed weakened absorption peaks corresponding to H-O stretching vibrations of bound water, H-O stretching vibrations of interlayer free water, and Si-O and Al-O stretching vibrations compared with pristine montmorillonite. These findings confirm that organic modification combined with zero-valent iron nanoparticle modification effectively reduced the mineralization degree of montmorillonite, thereby enhancing its adsorption and degradation capacity for TBBPA. The morphological and structural changes in nZVI@CMT not only verify the success of the modification but also provide critical evidence for mechanistic analysis based on surface structure and functional group alterations before and after reactions. The remediation effectiveness of nZVI@CMT was systematically evaluated by monitoring changes in TBBPA concentration, soil enzyme activity, and biological indicators (e.g., earthworm damage and seed germination). Additionally, LC-MS was used to identify reaction intermediates and deduce the potential TBBPA removal pathway by nZVI@CMT from soil. The results demonstrated that under natural aging conditions, the TBBPA removal rate in the contaminated soil group without nZVI@CMT addition was only 19.90% on day 42, whereas that in the group treated with nZVI@CMT showed a significant increase to 73.15% on day 42, indicating that nZVI@CMT effectively accelerated the TBBPA removal process, leading to a substantial reduction in TBBPA concentration in soil within a relatively short period. Moreover, nZVI@CMT was found to positively regulate soil enzyme activity, particularly enhancing urease activity, which is closely associated with the increased bacterial diversity and abundance facilitated by nZVI@CMT. Ecotoxicological tests showed that nZVI@CMT also effectively alleviated TBBPA-induced damage to earthworms. Compared to the contaminated group, earthworms in the nZVI@CMT-treated soil exhibited only minor effects such as blurred setae and slight dehydration in some segments, while the contaminated group displayed severe damage including body swelling, segment distortion, and epidermal cracking. Furthermore, nZVI@CMT improved seed germination rates and trends in contaminated soil. After treatment, the seed germination index increased from 2.95 to 4.33, and the seedling vigor index rose from 6.9 to 8.33, effectively mitigating the toxic effects of TBBPA on seedlings and demonstrating favorable remediation performance. Additionally, LC-MS analysis confirmed that the primary degradation pathways of TBBPA in soil included β-bond cleavage, demethylation, and benzene ring opening reactions. By extending the reaction time, the intermediate products could be further oxidized into small molecules such as carbon dioxide and water. In conclusion, this study systematically compared the TBBPA removal efficiencies of various montmorillonite-based materials, including MT, CMT, and nZVI@CMT. It confirmed that nZVI@CMT exhibits highly efficient and stable TBBPA removal. MT effectively addresses the agglomeration issue of nZVI and enhances the stability of nZVI particles. nZVI@CMT significantly accelerates TBBPA removal in soil. The primary degradation pathways of TBBPA involve β-bond cleavage, demethylation, and benzene ring opening, with complete mineralization achievable through extended reaction time or increased catalyst dosage. The addition of nZVI@CMT positively regulates soil physicochemical properties and enzyme activity, aiding in soil ecological restoration. nZVI@CMT reduces the toxicity of TBBPA to soil fauna, thereby maintaining ecological stability. Furthermore, nZVI@CMT improves the seed germination rate and germination potential in contaminated soil, alleviates the inhibitory effects of TBBPA on seed germination and seedling growth, and provides a foundation for vegetation restoration.

Key words: montmorillonite, organic modification, zero-valent iron nanoparticles (nZVI), tetrabromobisphenol A (TBBPA), soil remediation

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