IHEP OpenIR
Characterization of Ni-rich hexagonal birnessite and its geochemical effects on aqueous Pb2+/Zn2+ and As(III)
Yin, H; Tan, WF; Zheng LR(郑黎荣); Zheng, LR; Cui, HJ; Qiu, GH; Liu, F; Feng, XH
2012
Source PublicationGEOCHIMICA ET COSMOCHIMICA ACTA
Volume93Pages:47-62
AbstractHexagonal birnessite is the most ubiquitous manganese oxide in geological environments. It is often highly enriched in trace metal ions such as Ni and plays an important role in metal(loids) geochemistry. Nanostructured birnessites containing different amounts of Ni were synthesized by addition of Ni2+ to initial reactants. Powder X-ray diffraction (XRD), element analysis, field emission scanning electron microscopy (FE-SEM), X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA), X-ray absorption spectroscopy (XAS) and isothermal adsorption and oxidation of metal(loids) were carried out to investigate the effects of Ni doping on the substructure and physicochemical properties of birnessite, and Ni crystal chemistry in birnessite. These Ni-rich birnessites have Ni contents as high as 2.99% (Ni5) and 6.08% (Ni10) in weight. EXAFS results show that Ni5 has 23.7% of the total Ni (0.71 wt.%) and Ni10 has 34.5% of the total Ni (2.10 wt.%) in Mn octahedral layer with the remaining Ni located at vacancies and edge sites. The Ni-rich birnessites have weaker crystallinity and thermal stability, fewer layers stacked along the c axis, similar to 1.5-2.7 times larger surfaces areas, and a higher Mn average oxidation numbers (AONs) compared to the birnessite without Ni. Additionally, the doping of Ni during birnessite crystallization enhances the formation of vacancies in the layer; however, adsorption capacities for Pb2+ and Zn2+ by these Ni-rich birnessites are reduced, mainly because of vacancies and edge sites occupation by a large amount of Ni. The Ni-rich birnessites exhibit much higher oxidation capability and can completely oxidize As(III) in solution at rapid initial reaction rates under the experimental condition. The results indicate that incorporation of Ni into the natural birnessite in ferromanganese nodules may be achieved both by direct coprecipitation with Mn to build the layers and migration over time from adsorbed Ni on the surface into the layer structure. It is also implied that Ni doping in birnessite has great impact on the geochemical behaviors of heavy metals, either in adsorption or oxidation reactions. (C) 2012 Elsevier Ltd. All rights reserved.
Subject AreaGeochemistry & Geophysics
DOI10.1016/j.gca.2012.05.039
Indexed BySCI ; ADS
WOS IDWOS:000308426800004
ADS Bibcode2012GeCoA..93...47Y
ADS URLhttps://ui.adsabs.harvard.edu/abs/2012GeCoA..93...47Y
ADS CITATIONShttps://ui.adsabs.harvard.edu/abs/2012GeCoA..93...47Y/citations
Citation statistics
Cited Times:29 [ADS]
Document Type期刊论文
Identifierhttp://ir.ihep.ac.cn/handle/311005/223793
Collection中国科学院高能物理研究所
Recommended Citation
GB/T 7714
Yin, H,Tan, WF,Zheng LR,et al. Characterization of Ni-rich hexagonal birnessite and its geochemical effects on aqueous Pb2+/Zn2+ and As(III)[J]. GEOCHIMICA ET COSMOCHIMICA ACTA,2012,93:47-62.
APA Yin, H.,Tan, WF.,郑黎荣.,Zheng, LR.,Cui, HJ.,...&Feng, XH.(2012).Characterization of Ni-rich hexagonal birnessite and its geochemical effects on aqueous Pb2+/Zn2+ and As(III).GEOCHIMICA ET COSMOCHIMICA ACTA,93,47-62.
MLA Yin, H,et al."Characterization of Ni-rich hexagonal birnessite and its geochemical effects on aqueous Pb2+/Zn2+ and As(III)".GEOCHIMICA ET COSMOCHIMICA ACTA 93(2012):47-62.
Files in This Item:
File Name/Size DocType Version Access License
585.pdf(1061KB)期刊论文作者接受稿开放获取CC BY-NC-SAApplication Full Text
Related Services
Recommend this item
Bookmark
Usage statistics
Export to Endnote
Google Scholar
Similar articles in Google Scholar
[Yin, H]'s Articles
[Tan, WF]'s Articles
[郑黎荣]'s Articles
Baidu academic
Similar articles in Baidu academic
[Yin, H]'s Articles
[Tan, WF]'s Articles
[郑黎荣]'s Articles
Bing Scholar
Similar articles in Bing Scholar
[Yin, H]'s Articles
[Tan, WF]'s Articles
[郑黎荣]'s Articles
Terms of Use
No data!
Social Bookmark/Share
All comments (0)
No comment.
 

Items in the repository are protected by copyright, with all rights reserved, unless otherwise indicated.