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Lead and selenium distributions and speciation at biofilm/metal oxide interfaces.

机译:生物膜/金属氧化物界面处的铅和硒分布及形态。

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The geochemical cycling of trace elements in soil and aquatic systems is strongly influenced by sorption and precipitation reactions that occur at metal (hydr)oxide surfaces. However, the electrical and chemical properties of the mineral-water interface can be dramatically modified by the formation of highly hydrated, highly reactive microbial biofilms. We have developed synchrotron-based experimental approaches to quantitatively probe the distribution and speciation of Pb and Se sequestered within complex Burkholderia cepacia biofilms coating Al- and Fe-oxides. X-ray absorption spectroscopy was used to determine the speciation of the metal(loid) ions (e.g., mode of metal binding, changes in redox state) associated with the biofilms vs. the metal-oxide surfaces. XSW measurements were used to profile the vertical distribution of metal(loid) ions within microbial biofilms formed on single-crystal surfaces, and X-ray microscopy was used to map the lateral heterogeneities in metal(loid) distribution within the biofilms. The spectroscopic data were coupled to images of the biofilms obtained using epifluorescent, transmission electron (TEM) and scanning electron (SEM) microscopy.; X-ray standing wave data show that Pb and Se ions rapidly penetrate the Burkholderia cepacia biofilms and preferentially bind to highly reactive sites on the Al- and Fe-oxide surfaces. Once these reactive sites are saturated, sorption to surface functional groups present within the biofilms becomes quantitatively important. Therefore, B. cepacia biofilms do not passivate the intrinsic reactivity of the metal-oxide surfaces. Moreover, structural fitting of Pb LIII-EXAFS spectra collected for Pb(II) sorbed to B. cepacia/goethite composites, coupled to macroscopic uptake data, show that the presence of B. cepacia enhances Pb(II) uptake at goethite surfaces, primarily through the stabilization of bidentate, binuclear Pb(II) complexes.; The metabolic activity of B. cepacia has a dramatic effect on the speciation and bioavailability of Pb and Se. At micromolar Pb 2+ concentrations, B. cepacia induces the biomineralization of pyromorphite, a sparingly soluble Pb-phosphate phase, adjacent to the outer-membrane. For Se, B. cepacia catalyzes the rapid reduction of Se(IV) and partial reduction of Se(VI) to elemental Se(0). The Se species differentially segregate at the biofilm/metal-oxide interface, where Se(VI) and Se(0) are associated with the biofilms whereas Se(IV) is preferentially bound to the underlying mineral surface.
机译:土壤和水生系统中微量元素的地球化学循环受金属(氢氧化物)表面吸附和沉淀反应的强烈影响。但是,通过形成高度水合,高反应性的微生物生物膜,可以显着地改变矿泉水界面的电气和化学性质。我们已经开发了基于同步加速器的实验方法,以定量探测隔离在Al和Fe氧化物的复杂 Burkholderia cepacia 生物膜中隔离的Pb和Se的分布和形态。 X射线吸收光谱法用于确定与生物膜相对于金属氧化物表面相关的金属(金属)离子的形态(例如,金属结合的模式,氧化还原状态的变化)。 XSW测量用于描绘单晶表面上形成的微生物生物膜内金属(金属)离子的垂直分布,X射线显微镜用于绘制生物膜内金属(金属)分布的横向异质性。光谱数据与使用落射荧光,透射电子(TEM)和扫描电子(SEM)显微镜获得的生物膜的图像耦合。 X射线驻波数据表明,Pb和Se离子快速穿透<斜面伯克霍尔德菌>伯克霍尔德菌生物膜,并优先结合到Al和Fe氧化物表面的高反应位。一旦这些反应性位点饱和,对生物膜内存在的表面官能团的吸附就在定量上变得重要。因此,<斜体> B。芥蓝生物膜不会钝化金属氧化物表面的固有反应性。此外,针对吸附到 B的Pb(II)收集的Pb L III -EXAFS光谱的结构拟合。酒糟 /针铁矿复合材料,加上宏观吸收数据,表明存在 B。 cepacia 主要通过稳定双齿双核Pb(II)络合物来提高针铁矿表面Pb(II)的吸收。 B的代谢活性。洋葱头孢菌素对铅和硒的形态和生物利用度有显着影响。在微摩尔Pb 2 + 浓度下, B。 cepacia 诱导焦微晶石的生物矿化,焦微晶石是微溶的Pb-磷酸盐相,与外膜相邻。对于Se,<斜体> B。 cepacia 催化Se(IV)的快速还原和Se(VI)的部分还原为元素Se(0)。硒物种在生物膜/金属氧化物界面处不同地偏析,其中硒(VI)和硒(0)与生物膜相关,而硒(IV)优先结合在下面的矿物表面。

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