首页> 外文期刊>Geochemical Transactions >Absorption mechanisms of Cu2+ on a biogenic bixbyite-like Mn2O3 produced by Bacillus CUA isolated from soil
【24h】

Absorption mechanisms of Cu2+ on a biogenic bixbyite-like Mn2O3 produced by Bacillus CUA isolated from soil

机译:Cu 2 + 在土壤杆菌分离的生物型方铁锰矿型Mn 2 O 3 中的吸收机理

获取原文
           

摘要

Background Although most reported biogenic Mn oxides are hexagonal birnessites, other types of biogenic Mn oxides also commonly occur in the environment. However, sorption characteristics and underlying mechanisms of the adsorption of heavy-metal ions on these biogenic Mn oxides are still rarely addressed. In this study, the sorption mechanisms of Cu(II) on a low valence biogenic Mn oxide, poorly crystallized bixbyite-like Mn2O3 (α-Mn2O3), were investigated. Results The maximum adsorption capacity of Cu(II) onto this biogenic Mn oxide at pH 6.00 was 796 mmol/kg (0.45 mol Cu mol?1 Mn). The complex structure of adsorbed Cu(II) was constrained using Cu extended X-ray absorption fine structure (EXAFS) analysis, combined with structural parameters of the biogenic Mn oxide with alternately arranged regular and distorted MnO6 octahedra obtained through multiple-FEFF fitting of Mn EXAFS data. The sorbed Cu(II) was found to coordinate with the biogenic Mn oxide particle edges as inner-sphere complexes. At a relatively low Cu2+ loading (233 mmol/kg, pH 6.00), Cu(II) adsorbed onto the biogenic Mn oxide with two types of coordinated complexes, i.e., (1) coordinated with one regular/distorted MnO6 octahedron as a monodentate-mononuclear complex and (2) with two adjacent MnO6 octahedra as a bidentate-binuclear complex. While, at a relatively high Cu2+ loading (787 mmol/kg, pH 6.00), only one type of coordinated complex was constrained, the adsorbed Cu(II) coordinated with one regular/distorted MnO6 octahedron as a monodentate-mononuclear complex. Conclusions This research extends further insight into the bacterial Mn(II) oxidation in the environment and serves as a good reference for understanding the interactions between metal ions and biogenic low valence Mn oxides, which are still poorly explored either theoretically or practically.
机译:背景技术尽管大多数报道的生物锰氧化物是六角形的水钠锰矿,但是其他类型的生物锰氧化物也通常在环境中存在。然而,这些生物源性锰氧化物上重金属离子的吸附特性和潜在机理仍然很少得到解决。在这项研究中,研究了Cu(II)在低价生物成因的氧化锰,结晶度较弱的方铁矿状Mn2O3(α-Mn2O3)上的吸附机理。结果在pH 6.00下,Cu(II)在该生物氧化锰上的最大吸附容量为796 mmol / kg(0.45 mol Cu mol?1 Mn)。利用Cu扩展X射线吸收精细结构(EXAFS)分析约束了吸附的Cu(II)的复杂结构,结合了生物锰氧化物的结构参数,该锰氧化物具有交替排列的规则和扭曲的MnO6八面体,这是通过Mn的多次FEFF拟合获得的。 EXAFS数据。发现吸附的Cu(II)与生物锰氧化物颗粒边缘协调为内球络合物。在相对较低的Cu2 +负载量(233 mmol / kg,pH 6.00)下,Cu(II)通过两种配位配合物吸附到生物型Mn氧化物上,即(1)与一种规则/扭曲的MnO6八面体配位为单齿- (2)带有两个相邻的MnO6八面体作为双齿-双核复合物。在较高的Cu2 +负载量(787 mmol / kg,pH 6.00)下,仅约束了一种配位配合物,吸附的Cu(II)与一种规则/扭曲的MnO6八面体配位为单齿-单核配合物。结论这项研究进一步扩展了对环境中细菌Mn(II)氧化的深入了解,并为理解金属离子与生物价低价Mn氧化物之间的相互作用提供了很好的参考,无论从理论上还是在实践上都鲜为人知。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号