The preferential retention of Zn-VI over Zn-IV on birnessite during dissolution/desorption
Qin, ZJ; Yin, H; Wang, XM; Zhang, Q; Lan, S; Koopal, LK; Zheng, LR; Feng, XH; Liu, F; Zheng LR(郑黎荣)
2018
发表期刊APPLIED CLAY SCIENCE (IF:3.101[JCR-2016],3.391[5-Year])
ISSN0169-1317
EISSN1872-9053
卷号161页码:169-175
文章类型Article
摘要Zn is a common heavy metal in soils and sediments. In this study, the release behaviors of octahedral (Zn-IV) and tetrahedral (Zn-IV) Zn complexes on synthesized hexagonal birnessite were explored by solution chemistry method in combination with spectroscopic analysis. In acidic dissolution processes, the release of adsorbed Zn2+ from birnessite occurred into two stages: in the first stage, similar to 60% of Zn2+ was desorbed rapidly, with only 8% of Mn being released, and the ratio of Zn-VI/Zn-IV increased with time; in the second stage, the residual Zn2+ was mostly Zn-VI and released slowly at a nearly constant rate until complete dissolution of the matrix mineral was observed. During desorption of Zn2+ by Pb2+, the ratio of Zn-VI/Zn-IV on birnessite also increased, while the residual percentage of Zn-VI remained nearly constant. However, it is known that Zn-IV-triple corner-sharing (TCS) is more stable than Zn-VI-TCS, suggesting that part of the remaining Zn-IV-TCS on birnessite might transform to Zn-VI-TCS immediately when Zn-VI-TCS is replaced by H+ or Pb2+. Additionally, the possible distribution of Mn3+ and Zn-IV or the partial charge compensation by protons can lead to the preferential retention of Zn-IV on birnessite or the preferential re-adsorption of Zn-IV at the new edge sites. These results can provide new insights into the geochemical behavior of Zn2+ contaminant in soil and aquatic environments.
关键词Zinc coordination Birnessite Dissolution Desorption Extended X-ray absorption fine structure spectroscopy
DOI10.1016/j.clay.2018.04.017
关键词[WOS]X-RAY-DIFFRACTION ; METAL SORBED BIRNESSITE ; NA-RICH BIRNESSITE ; BIOGENIC MN-OXIDES ; HEXAGONAL-BIRNESSITE ; MANGANESE OXIDE ; HEAVY-METALS ; PHYLLOMANGANATE NANOPARTICLES ; ABSORPTION SPECTROSCOPY ; FERROMANGANESE COATINGS
收录类别SCI ; ADS ; EI
语种英语
WOS研究方向Chemistry ; Materials Science ; Mineralogy
WOS类目Chemistry, Physical ; Materials Science, Multidisciplinary ; Mineralogy
WOS记录号WOS:000436916600021
EI入藏号20181805119496
ADS Bibcode2018ApCS..161..169Q
ADS URLhttps://ui.adsabs.harvard.edu/abs/2018ApCS..161..169Q
ADS引文https://ui.adsabs.harvard.edu/abs/2018ApCS..161..169Q/citations
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被引频次:3 [ADS]
文献类型期刊论文
条目标识符https://ir.ihep.ac.cn/handle/311005/286084
专题中国科学院高能物理研究所_中国散裂中子源
多学科研究中心
东莞研究部
核技术应用研究中心
作者单位中国科学院高能物理研究所
第一作者单位中国科学院高能物理研究所
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GB/T 7714
Qin, ZJ,Yin, H,Wang, XM,et al. The preferential retention of Zn-VI over Zn-IV on birnessite during dissolution/desorption[J]. APPLIED CLAY SCIENCE,2018,161:169-175.
APA Qin, ZJ.,Yin, H.,Wang, XM.,Zhang, Q.,Lan, S.,...&郑黎荣.(2018).The preferential retention of Zn-VI over Zn-IV on birnessite during dissolution/desorption.APPLIED CLAY SCIENCE,161,169-175.
MLA Qin, ZJ,et al."The preferential retention of Zn-VI over Zn-IV on birnessite during dissolution/desorption".APPLIED CLAY SCIENCE 161(2018):169-175.
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