Sustainable dual-mechanism arsenic remediation by Rhodopseudomonas palustris: Synergistic adsorption-methylation and life cycle assessment

IF 9.1 Q2 ENGINEERING, ENVIRONMENTAL
Nishan Sengupta , Monika Sogani , Anees Y. Khan , Keshava Balakrishna , Jayana Rajvanshi , Zainab Syed , Samiksha Verma
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引用次数: 0

Abstract

Arsenic pollution in groundwater is a global health concern that requires long-term cleanup techniques. This study presents Rhodopseudomonas palustris biomass as a unique, eco-friendly option for arsenic detoxification, achieving levels below the WHO/EPA limit of 10 µg L⁻¹ through synergistic adsorption and enzymatic methylation. The biomass can successfully adsorb arsenate [As(V)] and arsenite [As(III)], with capacities of 92 ± 0.5 µg g⁻¹ and 127 ± 0.5 µg g⁻¹, respectively, following pseudo-first-order kinetics at near-neutral pH (6.7). HPLC-ICP-MS analysis showed that As(III) transforms into less dangerous dimethylarsinic acid (DMA) at 1.30 ± 0.28 µg L⁻¹, whereas As(V) displays minor methylation (<0.01 µg L⁻¹ DMA) as estimated by mass balance calculations, thus emphasising As(III)'s higher reactivity. FTIR and FESEM-EDAX confirm that arsenic binds to carboxyl and phosphate groups on the biomass surface. The technique maintains 70 % efficiency after three repetitive adsorption cycles, increasing cost-effectiveness. Life Cycle Assessment reveals an environmental footprint of 2.34 kg CO₂-eq/m³, 0.015 kg PO₄³⁻-eq, and 0.00015 kg 1,4-DCB-eq, offering a significant improvement over reverse osmosis (3.5 kg CO₂-eq/m³) and adsorption-only systems (2.8 kg CO₂-eq/m³) by leveraging biological methylation to minimize emissions and toxicity. This dual-functional strategy, which combines strong adsorption and biotransformation, provides a scalable, long-term sustainable solution for arsenic remediation in resource-constrained areas, aligning with global water safety goals and advancing bioremediation paradigms.

Abstract Image

古红假单胞菌对砷的持续双机制修复:协同吸附-甲基化和生命周期评价
地下水中的砷污染是一个全球性的健康问题,需要长期的清理技术。这项研究表明,palustris红脓单胞菌的生物量是一种独特的、生态友好的砷解毒选择,通过协同吸附和酶甲基化,可以达到低于WHO/EPA 10µg L的限制。在接近中性的pH值(6.7)下,生物质可以成功地吸附砷酸盐[As(V)]和亚砷酸盐[As(III)],其吸附量分别为92±0.5µg⁻¹和127±0.5µg⁻¹。HPLC-ICP-MS分析表明,As(III)在1.30±0.28µg L -毒血症时转化为危险性较低的二甲基larsinic酸(DMA),而As(V)则表现出轻微的甲基化(<;0.01µg L -毒血症),从而强调As(III)具有较高的反应性。FTIR和FESEM-EDAX证实,砷与生物质表面的羧基和磷酸基团结合。该技术在三次重复吸附循环后仍保持70%的效率,提高了成本效益。生命周期评估显示,环境足迹为2.34 kg CO₂-eq/m³,0.015 kg PO₄³-eq和0.00015 kg 1.4 - dcb -eq,通过利用生物甲基化来减少排放和毒性,显着改善了反渗透(3.5 kg CO₂-eq/m³)和仅吸附系统(2.8 kg CO₂-eq/m³)。这一双重功能战略结合了强吸附和生物转化,为资源受限地区的砷修复提供了可扩展的、长期可持续的解决方案,与全球水安全目标保持一致,并推进了生物修复范例。
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来源期刊
Journal of hazardous materials advances
Journal of hazardous materials advances Environmental Engineering
CiteScore
4.80
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