Rothish R. Nair , Jasmin G. Russel , V.R. Vaishna , Jiffin Sam , B. Krishnakumar , K.P. Prathish
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Batch adsorption experiments with the Mt-H-CTS and RAS modules were conducted to optimize key parameters, including pH, contact time, and sorbent dosage, achieving a maximum adsorption efficiency. The developed sorbent system demonstrated excellent perchlorate removal performance in batch-scale experiments, achieving a maximum adsorption capacity of 5 mg g<sup>−1</sup> within 45 min under neutral pH. A lab-scale pilot study with 5 L of perchlorate-contaminated water (25 mg L⁻¹) showed > 98 % removal using RAS modules. Furthermore, real-water application using samples collected from a perchlorate-contaminated (5 mg L⁻¹) community pond validated the field applicability of the RAS system. These findings were incorporated, and a conceptual design and theoretical calculations for scaling up are presented to ease the lab-to-field scale applications. 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引用次数: 0
摘要
水源中的高氯酸盐污染对环境和公共卫生构成重大挑战,需要高效、可扩展和可持续的处理解决方案。本研究提出了一种综合的高氯酸盐处理方法,结合了吸附和生物修复,利用可回收的吸附基质(RAS)系统,通过将功能化蒙脱土粘土-壳聚糖复合材料(Mt-H-CTS)印迹到柔性碳布基质上。RAS旨在有效解决传统方法在大量水中有毒高氯酸盐离子净化方面的挑战和局限性,同时确保工艺安全性和循环性。利用Mt-H-CTS和RAS模块进行了批量吸附实验,优化了pH、接触时间、吸附剂用量等关键参数,获得了最大的吸附效率。开发的吸附剂系统在批量实验中表现出优异的高氯酸盐去除性能,在中性ph下在45 min内达到5 mg g−1的最大吸附量。在实验室规模的中试研究中,使用RAS模块对5 L高氯酸盐污染的水(25 mg L - 1)进行了>; 98 %的去除。此外,从高氯酸盐污染的(5 mg L - 1)社区池塘采集的实际水应用验证了RAS系统的现场适用性。这些发现被纳入,并提出了扩大规模的概念设计和理论计算,以简化实验室到现场的规模应用。此外,该研究通过提出一种利用综合生物修复策略从废吸附剂(RAS)中去除高氯酸盐的新方法,解决了与废吸附剂材料相关的挑战。这种方法对于确保吸附剂安全处置的经济可行性,同时提高其可重复使用性至关重要。在去污率、可重用性和更快的动力学(12 hr vs -à-vis 5天)方面,已经阐明了离地vis-à-vis原位生物修复性能更好的机理观点,从而清楚地揭示了开发的新型ras偶联生物修复策略的实际应用潜力。
Development of a scalable adsorptive bioremediation approach for perchlorate decontamination in water resources: A step towards process safety and circularity
Perchlorate contamination in water sources poses a significant environmental and public health challenge, necessitating efficient, scalable, and sustainable treatment solutions. This study presents an integrated perchlorate treatment approach that combines adsorption and bioremediation, utilizing a retrievable adsorbent substrate (RAS) system developed by imprinting a functionalized montmorillonite clay-chitosan composite (Mt-H-CTS) onto a flexible carbon cloth substrate. The RAS was designed to effectively address the challenges and limitations of conventional methods for the decontamination of toxic perchlorate ions in large volumes of water, while ensuring process safety and circularity. Batch adsorption experiments with the Mt-H-CTS and RAS modules were conducted to optimize key parameters, including pH, contact time, and sorbent dosage, achieving a maximum adsorption efficiency. The developed sorbent system demonstrated excellent perchlorate removal performance in batch-scale experiments, achieving a maximum adsorption capacity of 5 mg g−1 within 45 min under neutral pH. A lab-scale pilot study with 5 L of perchlorate-contaminated water (25 mg L⁻¹) showed > 98 % removal using RAS modules. Furthermore, real-water application using samples collected from a perchlorate-contaminated (5 mg L⁻¹) community pond validated the field applicability of the RAS system. These findings were incorporated, and a conceptual design and theoretical calculations for scaling up are presented to ease the lab-to-field scale applications. Moreover, the study addresses the challenges associated with spent adsorbent materials by presenting a novel approach to decontaminate perchlorate from spent sorbent (RAS) using an integrated bioremediation strategy. This approach is crucial for ensuring the economic feasibility of safe sorbent disposal while enhancing its reusability. The mechanistic perspective of better performance of ex-situ vis-à-vis in-situ bioremediation in terms of % decontamination, reusability, and faster kinetics (12 hr vis-à-vis 5 days) has been illustrated, thereby clearly unveiling the practical application potential of the developed novel RAS-coupled bioremediation strategy.
期刊介绍:
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