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| Main Authors: | , , , , , , |
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| Format: | Preprint |
| Published: |
2026
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| Subjects: | |
| Online Access: | https://arxiv.org/abs/2603.22144 |
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| _version_ | 1866911538342789120 |
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| author | Ngambia, Audrey Gavrilova, Anastasiia Huang, Haitao Lyu, Zhuodong Mašek, Ondřej Graham, Margaret Erastova, Valentina |
| author_facet | Ngambia, Audrey Gavrilova, Anastasiia Huang, Haitao Lyu, Zhuodong Mašek, Ondřej Graham, Margaret Erastova, Valentina |
| contents | Manganese(II) mobilised by mining activity poses a persistent water-quality challenge, yet the mechanisms by which low-cost sorbents, such as biochar, sequester Mn(II) remain poorly resolved. This study identifies the specific chemical drivers of Mn(II) sequestration by combining fixed-bed column and batch experiments with atomistic molecular dynamics simulations. Oilseed rape straw biochars, produced at 350\textdegree C, 550\textdegree C, and 700\textdegree C, removed 20-50% of dissolved Mn from acidic influent (pH 4, 5 ppm). High-temperature biochar achieved the greatest removal ($\sim$50%) and rapidly increased effluent pH to 9, triggering alkaline precipitation. Conversely, lower-temperature biochars removed 20-30% of Mn while maintaining a near-neutral pH (7-7.5). Enhanced \ce{K+} release in these systems indicates significant cation exchange and non-precipitative pathways. Molecular simulations confirmed that while neutral surfaces show weak Mn(II) association, deprotonated sites drive strong adsorption through inner-sphere complexation ($\sim$50% removal) and outer-sphere association ($\sim$10%). These results establish a mechanistic framework to distinguish between precipitation-led and surface-complexation-led removal. By providing specific chemical criteria for Mn-targeted sequestration, this work enables the rational design of engineered biochars for sustainable water remediation. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2603_22144 |
| institution | arXiv |
| publishDate | 2026 |
| record_format | arxiv |
| spellingShingle | Decoupling Precipitation and Surface Complexation during Mn(II) Removal by Biochar via Experiments and Atomistic Simulations Ngambia, Audrey Gavrilova, Anastasiia Huang, Haitao Lyu, Zhuodong Mašek, Ondřej Graham, Margaret Erastova, Valentina Materials Science Other Condensed Matter Chemical Physics Manganese(II) mobilised by mining activity poses a persistent water-quality challenge, yet the mechanisms by which low-cost sorbents, such as biochar, sequester Mn(II) remain poorly resolved. This study identifies the specific chemical drivers of Mn(II) sequestration by combining fixed-bed column and batch experiments with atomistic molecular dynamics simulations. Oilseed rape straw biochars, produced at 350\textdegree C, 550\textdegree C, and 700\textdegree C, removed 20-50% of dissolved Mn from acidic influent (pH 4, 5 ppm). High-temperature biochar achieved the greatest removal ($\sim$50%) and rapidly increased effluent pH to 9, triggering alkaline precipitation. Conversely, lower-temperature biochars removed 20-30% of Mn while maintaining a near-neutral pH (7-7.5). Enhanced \ce{K+} release in these systems indicates significant cation exchange and non-precipitative pathways. Molecular simulations confirmed that while neutral surfaces show weak Mn(II) association, deprotonated sites drive strong adsorption through inner-sphere complexation ($\sim$50% removal) and outer-sphere association ($\sim$10%). These results establish a mechanistic framework to distinguish between precipitation-led and surface-complexation-led removal. By providing specific chemical criteria for Mn-targeted sequestration, this work enables the rational design of engineered biochars for sustainable water remediation. |
| title | Decoupling Precipitation and Surface Complexation during Mn(II) Removal by Biochar via Experiments and Atomistic Simulations |
| topic | Materials Science Other Condensed Matter Chemical Physics |
| url | https://arxiv.org/abs/2603.22144 |