Pb(II) distributions at biofilm-metal oxide interfaces

被引:110
作者
Templeton, AS [1 ]
Trainor, TP
Traina, SJ
Spormann, AM
Brown, GE
机构
[1] Stanford Univ, Stanford, CA 94035 USA
[2] Ohio State Univ, Sch Nat Resources, Columbus, OH 43210 USA
[3] Stanford Linear Accelerator Ctr, Stanford Synchrotron Radiat Lab, Menlo Pk, CA 94025 USA
关键词
D O I
10.1073/pnas.201150998
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The distribution of aqueous Pb(II) sorbed at the interface between Burkholderia cepacia biofilms and hematite (alpha -Fe2O3) or corundum (alpha -Al2O3) surfaces has been probed by using an application of the long-period x-ray standing wave technique. Attached bacteria and adsorbed organic matter may interfere with sorption processes on metal oxide surfaces by changing the characteristics of the electrical double layer at the solid-solution interface, blocking surface sites, or providing a variety of new sites for metal binding. In this work, Pb L-alpha fluorescence yield profiles for samples equilibrated with 10(-7) to 10(-3.8) M Pb(II) were measured and modeled to determine quantitatively the partitioning of Pb(II) at the biofilm-metal oxide interface. Our data show that the reactive sites on the metal oxide surfaces were not passivated by the formation of a monolayer biofilm. Instead, high-energy surface sites on the metal oxides form the dominant sink for Pb(II) at submicromolar concentrations, following the trend alpha -Fe2O3 (0001) > alpha -Al2O3 (11-over-bar-02) > alpha -Al2O3 (0001), despite the greater site density within the overlying biofilms. At [Pb] > 10(-6) M, significant Pb uptake by the biofilms was observed.
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页码:11897 / 11902
页数:6
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