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Enhanced removal of heavy metal ions from aqueous solution using manganese dioxide-loaded biochar: Behavior and mechanism.

ABSTRACT: In this study, a redox precipitation method was used to load manganese dioxide (MnO2) nanoparticles on biochar (BC) (BC@MnO2) pyrolyzed from the invasive water hyacinth, and the adsorption of Cd(II),Cu(II), Zn(II), and Pb(II) was investigated. Several techniques were used to characterize the adsorbents. The results revealed that the BC surface was covered by many intertwined thin amorphous MnO2 nanosheets, which significantly increased its specific surface area and pore volume. The adsorption of heavy metal ions by BC was negligible, whereas the MnO2-containing adsorbents exhibited a high capacity for adsorbing heavy metal ions. However, the MnO2-normalized adsorption amount decreased with increasing MnO2 load and was largely unchanged at MnO2 loads of 26.6% to 30.2%. The capacity for adsorbing heavy metal ions of BC@MnO2 was pH-dependent, but the adsorption affinity was unaffected by coexisting ions. Column tests revealed that BC@MnO2 with a load of 26.6% had a high capacity for removing heavy metal ions from simulated and real electroplating wastewater. Therefore, BC@MnO2 with a load of 26.6% shows promise as a regenerable adsorbent for removing heavy metal ions from water/wastewater. This study could lay an essential foundation to develop a win-win strategy for heavy metal ions removal from wastewater using biochar derived from water hyacinth.

SUBMITTER: Zhang H

PROVIDER: S-EPMC7142110 | biostudies-literature | 2020 Apr

REPOSITORIES: biostudies-literature

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Enhanced removal of heavy metal ions from aqueous solution using manganese dioxide-loaded biochar: Behavior and mechanism.

Zhang Haipeng H Xu Fangfang F Xue Jinyuan J Chen Shiyong S Wang Juanjuan J Yang Yanju Y

Scientific reports 20200408 1

In this study, a redox precipitation method was used to load manganese dioxide (MnO2) nanoparticles on biochar (BC) (BC@MnO2) pyrolyzed from the invasive water hyacinth, and the adsorption of Cd(II),Cu(II), Zn(II), and Pb(II) was investigated. Several techniques were used to characterize the adsorbents. The results revealed that the BC surface was covered by many intertwined thin amorphous MnO2 nanosheets, which significantly increased its specific surface area a ...[more]

PMID: 32269275

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Project description:Halloysite nanotubes (HNT) and ball-milled biochar (BC) incorporated biocompatible mesoporous adsorbents (HNT-BC@Alg) were synthesized for adsorption of aqueous heavy-metal ions. HNT-BC@Alg outperformed the BC, HNT, and BC@Alg in removing cadmium (Cd), copper (Cu), nickel (Ni), and lead (Pb). Mesoporous structure (∼7.19 to 7.56 nm) of HNT-BC@Alg was developed containing an abundance of functional groups induced from encapsulated BC and tubular HNT, which allowed heavy metals to infiltrate and interact with the adsorbents. Siloxane groups from HNT, oxygen-containing functional groups from BC, and hydroxyl and carboxyl groups from alginate polymer play a significant role in the adsorption of heavy-metal ions. The removal percentage of heavy metals was recorded as Pb (∼99.97 to 99.05%) > Cu (∼95.01 to 90.53%) > Cd (∼92.5 to 55.25%) > Ni (∼80.85 to 50.6%), even in the presence of 0.01/0.001 M of CaCl2 and Na2SO4 as background electrolytes and charged organic molecule under an environmentally relevant concentration (200 μg/L). The maximum adsorption capacities of Ni, Cd, Cu, and Pb were calculated as 2.85 ± 0.08, 6.96 ± 0.31, 16.87 ± 1.50, and 26.49 ± 2.04 mg/g, respectively. HNT-BC@Alg has fast sorption kinetics and maximum adsorption capacity within a short contact time (∼2 h). Energy-dispersive X-ray spectroscopy (EDS) elemental mapping exhibited that adsorbed heavy metals co-distributed with Ca, Si, and Al. The reduction of surface area, pore volume, and pore area of HNT-BC@Alg (after sorption of heavy metals) confirms that mesoporous surface (2-18 nm) supports diffusion, infiltration, and interaction. However, a lower range of mesoporous diameter of the adsorbent is more suitable for the adsorption of heavy-metal ions. The adsorption isotherm and kinetics fitted well with the Langmuir isotherm and the pseudo-second-order kinetic models, demonstrating the monolayer formation of heavy-metal ions through both the physical sorption and chemical sorption, including pore filling, ion exchange, and electrostatic interaction.

Project description:The hydration of the alkali metal ions in aqueous solution has been studied by large angle X-ray scattering (LAXS) and double difference infrared spectroscopy (DDIR). The structures of the dimethyl sulfoxide solvated alkali metal ions in solution have been determined to support the studies in aqueous solution. The results of the LAXS and DDIR measurements show that the sodium, potassium, rubidium and cesium ions all are weakly hydrated with only a single shell of water molecules. The smaller lithium ion is more strongly hydrated, most probably with a second hydration shell present. The influence of the rubidium and cesium ions on the water structure was found to be very weak, and it was not possible to quantify this effect in a reliable way due to insufficient separation of the O-D stretching bands of partially deuterated water bound to these metal ions and the O-D stretching bands of the bulk water. Aqueous solutions of sodium, potassium and cesium iodide and cesium and lithium hydroxide have been studied by LAXS and M-O bond distances have been determined fairly accurately except for lithium. However, the number of water molecules binding to the alkali metal ions is very difficult to determine from the LAXS measurements as the number of distances and the temperature factor are strongly correlated. A thorough analysis of M-O bond distances in solid alkali metal compounds with ligands binding through oxygen has been made from available structure databases. There is relatively strong correlation between M-O bond distances and coordination numbers also for the alkali metal ions even though the M-O interactions are weak and the number of complexes of potassium, rubidium and cesium with well-defined coordination geometry is very small. The mean M-O bond distance in the hydrated sodium, potassium, rubidium and cesium ions in aqueous solution have been determined to be 2.43(2), 2.81(1), 2.98(1) and 3.07(1) Å, which corresponds to six-, seven-, eight- and eight-coordination. These coordination numbers are supported by the linear relationship of the hydration enthalpies and the M-O bond distances. This correlation indicates that the hydrated lithium ion is four-coordinate in aqueous solution. New ionic radii are proposed for four- and six-coordinate lithium(I), 0.60 and 0.79 Å, respectively, as well as for five- and six-coordinate sodium(I), 1.02 and 1.07 Å, respectively. The ionic radii for six- and seven-coordinate K(+), 1.38 and 1.46 Å, respectively, and eight-coordinate Rb(+) and Cs(+), 1.64 and 1.73 Å, respectively, are confirmed from previous studies. The M-O bond distances in dimethyl sulfoxide solvated sodium, potassium, rubidium and cesium ions in solution are very similar to those observed in aqueous solution.

Dataset Information

Enhanced removal of heavy metal ions from aqueous solution using manganese dioxide-loaded biochar: Behavior and mechanism.

Publications

Enhanced removal of heavy metal ions from aqueous solution using manganese dioxide-loaded biochar: Behavior and mechanism.

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