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Monitoring the fate of copper nanoparticles in river biofilms using scanning transmission X-ray microscopy (STXM)

机译:使用扫描透射X射线显微镜(STXM)监测河流生物膜中铜纳米颗粒的命运

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Scanning transmission X-ray microscopy (STXM) at the C 1s and Cu 2p edges was used to study the fate of Cu nanoparticles, including their sorption-dissolution, speciation and distribution in a complex natural river biofilm exposed to 1mgL ~(-1) Cu nanoparticles for 5min, 3days or 7days. The original Cu nanoparticles, ~30nm in diameter, were composed of Cu(I) and Cu(II) species, presumably a Cu(I) core surrounded by oxidized Cu(II). When the Cu nanoparticles were initially added to the biofilm, Cu nanoparticles were occasionally found as individual particles but most frequently were observed as aggregates. The aggregates were in association with diatoms and the extracellular polymeric substances (EPS) of the biofilm. In addition, a new Cu(II) species, as evident from a shift in its peak position (-0.4eV) relative to the Cu nanoparticles, was found to be sorbed by the diatoms after 5min and was still detected after 7days. Evidently, the Cu nanoparticles had undergone dissolution, followed by sorption of ionic Cu(II) by the diatoms. The bacteria and cyanobacteria in the biofilm did not apparently sorb detectable amounts of Cu at any time. C 1s measurements indicated that the Cu(II) from solution was sorbed by the lipid-rich extracellular polymeric substances associated with the diatoms. These observations demonstrated that both the Cu nanoparticles and dissolution products remained associated with the river biofilm through interactions with specific biopolymers up to 7days following exposure. Therefore, for some metal nanomaterials, sorption of the solid phase with subsequent dissolution and re-sorption are significant with respect to their chemodynamics and effects on the biofilm, especially when trophic transfer events are considered. Importantly, these interactions provide an entry point for copper into the aquatic food web.
机译:使用C 1s和Cu 2p边缘的扫描透射X射线显微镜(STXM)来研究Cu纳米颗粒的命运,包括它们在1mgL〜(-1)的复杂天然河流生物膜中的吸附-溶解,形态和分布。铜纳米颗粒持续5分钟,3天或7天。直径约30nm的原始Cu纳米粒子由Cu(I)和Cu(II)物种组成,大概是被氧化的Cu(II)包围的Cu(I)核。当最初将Cu纳米颗粒添加到生物膜中时,偶尔发现Cu纳米颗粒为单个颗粒,但最常见的是聚集体。聚集体与硅藻和生物膜的细胞外聚合物(EPS)有关。此外,从相对于铜纳米颗粒的峰位置(-0.4eV)的变化可以明显看出,一种新的Cu(II)物种在5分钟后被硅藻吸附,并在7天后仍被检测到。显然,铜纳米颗粒已经溶解,随后硅藻吸附了离子型Cu(II)。生物膜中的细菌和蓝细菌在任何时候都没有明显吸收可检测量的Cu。 C 1s测量表明,溶液中的Cu(II)被与硅藻相关的富含脂质的细胞外聚合物吸附。这些观察结果表明,暴露后长达7天,Cu纳米颗粒和溶解产物都通过与特定生物聚合物的相互作用而仍与河流生物膜相关。因此,对于某些金属纳米材料,固相的吸附以及随后的溶解和再吸附在其化学动力学和对生物膜的影响方面非常重要,尤其是在考虑了营养传递事件时。重要的是,这些相互作用为铜进入水生食物网提供了切入点。

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