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Removal and Recovery of Toxic Silver Ion Using Deep-Sea Bacterial Generated Biogenic Manganese Oxides

Products containing silver ion (Ag(+)) are widely used, leading to a large amount of Ag(+)-containing waste. The deep-sea manganese-oxidizing bacterium Marinobacter sp. MnI7-9 efficiently oxidizes Mn(2+) to generate biogenic Mn oxide (BMO). The potential of BMO for recovering metal ions by adsorptio...

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Autores principales: Pei, Yuanjun, Chen, Xiao, Xiong, Dandan, Liao, Shuijiao, Wang, Gejiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3847083/
https://www.ncbi.nlm.nih.gov/pubmed/24312566
http://dx.doi.org/10.1371/journal.pone.0081627
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author Pei, Yuanjun
Chen, Xiao
Xiong, Dandan
Liao, Shuijiao
Wang, Gejiao
author_facet Pei, Yuanjun
Chen, Xiao
Xiong, Dandan
Liao, Shuijiao
Wang, Gejiao
author_sort Pei, Yuanjun
collection PubMed
description Products containing silver ion (Ag(+)) are widely used, leading to a large amount of Ag(+)-containing waste. The deep-sea manganese-oxidizing bacterium Marinobacter sp. MnI7-9 efficiently oxidizes Mn(2+) to generate biogenic Mn oxide (BMO). The potential of BMO for recovering metal ions by adsorption has been investigated for some ions but not for Ag(+). The main aim of this study was to develop effective methods for adsorbing and recovering Ag using BMO produced by Marinobacter sp. MnI7-9. In addition, the adsorption mechanism was determined using X-ray photoelectron spectroscopy analysis, specific surface area analysis, adsorption kinetics and thermodynamics. The results showed that BMO had a higher adsorption capacity for Ag(+) compared to the chemical synthesized MnO(2) (CMO). The isothermal absorption curves of BMO and CMO both fit the Langmuir model well and the maximum adsorption capacities at 28°C were 8.097 mmol/g and 0.787 mmol/g, for BMO and CMO, respectively. The change in enthalpy (ΔH(θ)) for BMO was 59.69 kJ/mol indicating that it acts primarily by chemical adsorption. The change in free energy (ΔG(θ)) for BMO was negative, which suggests that the adsorption occurs spontaneously. Ag(+) adsorption by BMO was driven by entropy based on the positive ΔS(θ) values. The Ag(+) adsorption kinetics by BMO fit the pseudo-second order model and the apparent activation energy of E(a) is 21.72 kJ/mol. X-ray photoelectron spectroscopy analysis showed that 15.29% Ag(+) adsorbed by BMO was transferred to Ag(0) and meant that redox reaction had happened during the adsorption. Desorption using nitric acid and Na(2)S completely recovered the Ag. The results show that BMO produced by strain MnI7-9 has potential for bioremediation and reutilization of Ag(+)-containing waste.
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spelling pubmed-38470832013-12-05 Removal and Recovery of Toxic Silver Ion Using Deep-Sea Bacterial Generated Biogenic Manganese Oxides Pei, Yuanjun Chen, Xiao Xiong, Dandan Liao, Shuijiao Wang, Gejiao PLoS One Research Article Products containing silver ion (Ag(+)) are widely used, leading to a large amount of Ag(+)-containing waste. The deep-sea manganese-oxidizing bacterium Marinobacter sp. MnI7-9 efficiently oxidizes Mn(2+) to generate biogenic Mn oxide (BMO). The potential of BMO for recovering metal ions by adsorption has been investigated for some ions but not for Ag(+). The main aim of this study was to develop effective methods for adsorbing and recovering Ag using BMO produced by Marinobacter sp. MnI7-9. In addition, the adsorption mechanism was determined using X-ray photoelectron spectroscopy analysis, specific surface area analysis, adsorption kinetics and thermodynamics. The results showed that BMO had a higher adsorption capacity for Ag(+) compared to the chemical synthesized MnO(2) (CMO). The isothermal absorption curves of BMO and CMO both fit the Langmuir model well and the maximum adsorption capacities at 28°C were 8.097 mmol/g and 0.787 mmol/g, for BMO and CMO, respectively. The change in enthalpy (ΔH(θ)) for BMO was 59.69 kJ/mol indicating that it acts primarily by chemical adsorption. The change in free energy (ΔG(θ)) for BMO was negative, which suggests that the adsorption occurs spontaneously. Ag(+) adsorption by BMO was driven by entropy based on the positive ΔS(θ) values. The Ag(+) adsorption kinetics by BMO fit the pseudo-second order model and the apparent activation energy of E(a) is 21.72 kJ/mol. X-ray photoelectron spectroscopy analysis showed that 15.29% Ag(+) adsorbed by BMO was transferred to Ag(0) and meant that redox reaction had happened during the adsorption. Desorption using nitric acid and Na(2)S completely recovered the Ag. The results show that BMO produced by strain MnI7-9 has potential for bioremediation and reutilization of Ag(+)-containing waste. Public Library of Science 2013-12-02 /pmc/articles/PMC3847083/ /pubmed/24312566 http://dx.doi.org/10.1371/journal.pone.0081627 Text en © 2013 Pei et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Pei, Yuanjun
Chen, Xiao
Xiong, Dandan
Liao, Shuijiao
Wang, Gejiao
Removal and Recovery of Toxic Silver Ion Using Deep-Sea Bacterial Generated Biogenic Manganese Oxides
title Removal and Recovery of Toxic Silver Ion Using Deep-Sea Bacterial Generated Biogenic Manganese Oxides
title_full Removal and Recovery of Toxic Silver Ion Using Deep-Sea Bacterial Generated Biogenic Manganese Oxides
title_fullStr Removal and Recovery of Toxic Silver Ion Using Deep-Sea Bacterial Generated Biogenic Manganese Oxides
title_full_unstemmed Removal and Recovery of Toxic Silver Ion Using Deep-Sea Bacterial Generated Biogenic Manganese Oxides
title_short Removal and Recovery of Toxic Silver Ion Using Deep-Sea Bacterial Generated Biogenic Manganese Oxides
title_sort removal and recovery of toxic silver ion using deep-sea bacterial generated biogenic manganese oxides
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3847083/
https://www.ncbi.nlm.nih.gov/pubmed/24312566
http://dx.doi.org/10.1371/journal.pone.0081627
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