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    Rights statement: This is the author’s version of a work that was accepted for publication in Chemosphere. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Chemosphere, 261, 2020 DOI: 10.1016/j.chemosphere.2020.128220

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Sorption mechanisms of lead on soil-derived black carbon formed under varying cultivation systems

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Sorption mechanisms of lead on soil-derived black carbon formed under varying cultivation systems. / Zhao, Qingjie; Li, Jianhong; Sarkar, Binoy et al.
In: Chemosphere, Vol. 261, 128220, 01.12.2020.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Zhao, Q, Li, J, Sarkar, B, Wu, W, Li, B, Liu, R, Nawaz, M, Zia-ur-Rehman, M, Wang, H & Wu, Z 2020, 'Sorption mechanisms of lead on soil-derived black carbon formed under varying cultivation systems', Chemosphere, vol. 261, 128220. https://doi.org/10.1016/j.chemosphere.2020.128220

APA

Zhao, Q., Li, J., Sarkar, B., Wu, W., Li, B., Liu, R., Nawaz, M., Zia-ur-Rehman, M., Wang, H., & Wu, Z. (2020). Sorption mechanisms of lead on soil-derived black carbon formed under varying cultivation systems. Chemosphere, 261, Article 128220. https://doi.org/10.1016/j.chemosphere.2020.128220

Vancouver

Zhao Q, Li J, Sarkar B, Wu W, Li B, Liu R et al. Sorption mechanisms of lead on soil-derived black carbon formed under varying cultivation systems. Chemosphere. 2020 Dec 1;261:128220. Epub 2020 Sept 3. doi: 10.1016/j.chemosphere.2020.128220

Author

Bibtex

@article{3b419baece424ef18b1fa31a848d9a1c,
title = "Sorption mechanisms of lead on soil-derived black carbon formed under varying cultivation systems",
abstract = "The knowledge about lead (Pb) sorption on soil-derived black carbons (SBCs) under different cultivation intensities of soils is limited. In this study, chemical and spectroscopic methods were applied to investigate the Pb sorption mechanisms on SBCs in soils from a forest land, a rubber plantation area, and a vegetable farm with none, less and highly intensive cultivation, respectively, that are located in the Hainan Island of China. Results showed that the specific surface area and cation exchange capacity of the SBCs from the less and highly intensive cultivation soils were 4.5- and 2.7-fold, and 1.3- and 1.8-fold higher compared to that of SBC from the no-cultivation soil, which subsequently enhanced the Pb sorption capacities of SBCs in iron exchange fraction. Ion exchange and hydrogen bonded Pb fractions together accounted for about 80% of total Pb sorbed on all SBCs at an externally added 1000 mg L−1 Pb solution concentration. The Odouble bondC–O groups also played key roles in Pb sorption by forming complexes of Odouble bondC–O–Pb–O and/or Odouble bondC–O–Pb. Overall, SBCs in soils under all studied cultivation intensities showed high potential to sorb Pb (with the maximum absorbed Pb amount of 46.0–91.3 mg g−1), and increased Pb sorption capacities of the studied soils by 18.7–21.1 mg kg−1 in the stable fraction (complexation). Therefore, SBC might be a potential environment-friendly material to enhance the Pb immobilization capacity of soil.",
author = "Qingjie Zhao and Jianhong Li and Binoy Sarkar and Weidong Wu and Boling Li and Ruichun Liu and Mohsin Nawaz and Muhammad Zia-ur-Rehman and Hailong Wang and Zhipeng Wu",
note = "This is the author{\textquoteright}s version of a work that was accepted for publication in Chemosphere. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Chemosphere, 261, 2020 DOI: 10.1016/j.chemosphere.2020.128220",
year = "2020",
month = dec,
day = "1",
doi = "10.1016/j.chemosphere.2020.128220",
language = "English",
volume = "261",
journal = "Chemosphere",
issn = "0045-6535",
publisher = "NLM (Medline)",

}

RIS

TY - JOUR

T1 - Sorption mechanisms of lead on soil-derived black carbon formed under varying cultivation systems

AU - Zhao, Qingjie

AU - Li, Jianhong

AU - Sarkar, Binoy

AU - Wu, Weidong

AU - Li, Boling

AU - Liu, Ruichun

AU - Nawaz, Mohsin

AU - Zia-ur-Rehman, Muhammad

AU - Wang, Hailong

AU - Wu, Zhipeng

N1 - This is the author’s version of a work that was accepted for publication in Chemosphere. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Chemosphere, 261, 2020 DOI: 10.1016/j.chemosphere.2020.128220

PY - 2020/12/1

Y1 - 2020/12/1

N2 - The knowledge about lead (Pb) sorption on soil-derived black carbons (SBCs) under different cultivation intensities of soils is limited. In this study, chemical and spectroscopic methods were applied to investigate the Pb sorption mechanisms on SBCs in soils from a forest land, a rubber plantation area, and a vegetable farm with none, less and highly intensive cultivation, respectively, that are located in the Hainan Island of China. Results showed that the specific surface area and cation exchange capacity of the SBCs from the less and highly intensive cultivation soils were 4.5- and 2.7-fold, and 1.3- and 1.8-fold higher compared to that of SBC from the no-cultivation soil, which subsequently enhanced the Pb sorption capacities of SBCs in iron exchange fraction. Ion exchange and hydrogen bonded Pb fractions together accounted for about 80% of total Pb sorbed on all SBCs at an externally added 1000 mg L−1 Pb solution concentration. The Odouble bondC–O groups also played key roles in Pb sorption by forming complexes of Odouble bondC–O–Pb–O and/or Odouble bondC–O–Pb. Overall, SBCs in soils under all studied cultivation intensities showed high potential to sorb Pb (with the maximum absorbed Pb amount of 46.0–91.3 mg g−1), and increased Pb sorption capacities of the studied soils by 18.7–21.1 mg kg−1 in the stable fraction (complexation). Therefore, SBC might be a potential environment-friendly material to enhance the Pb immobilization capacity of soil.

AB - The knowledge about lead (Pb) sorption on soil-derived black carbons (SBCs) under different cultivation intensities of soils is limited. In this study, chemical and spectroscopic methods were applied to investigate the Pb sorption mechanisms on SBCs in soils from a forest land, a rubber plantation area, and a vegetable farm with none, less and highly intensive cultivation, respectively, that are located in the Hainan Island of China. Results showed that the specific surface area and cation exchange capacity of the SBCs from the less and highly intensive cultivation soils were 4.5- and 2.7-fold, and 1.3- and 1.8-fold higher compared to that of SBC from the no-cultivation soil, which subsequently enhanced the Pb sorption capacities of SBCs in iron exchange fraction. Ion exchange and hydrogen bonded Pb fractions together accounted for about 80% of total Pb sorbed on all SBCs at an externally added 1000 mg L−1 Pb solution concentration. The Odouble bondC–O groups also played key roles in Pb sorption by forming complexes of Odouble bondC–O–Pb–O and/or Odouble bondC–O–Pb. Overall, SBCs in soils under all studied cultivation intensities showed high potential to sorb Pb (with the maximum absorbed Pb amount of 46.0–91.3 mg g−1), and increased Pb sorption capacities of the studied soils by 18.7–21.1 mg kg−1 in the stable fraction (complexation). Therefore, SBC might be a potential environment-friendly material to enhance the Pb immobilization capacity of soil.

U2 - 10.1016/j.chemosphere.2020.128220

DO - 10.1016/j.chemosphere.2020.128220

M3 - Journal article

VL - 261

JO - Chemosphere

JF - Chemosphere

SN - 0045-6535

M1 - 128220

ER -