Gomez Mario Alberto, Jiang Ruonan, Song Miao, Li Dongsheng, Lea Alan Scott, Ma Xu, Wang Haibo, Yin Xiuling, Wang Shaofeng, Jia Yongfeng
Liaoning Engineering Research Center for Treatment and Recycling of Industrially Discharged Heavy Metals, Shenyang University of Chemical Technology Shenyang Liaoning 110142 China
Department of Geological Sciences, University of Saskatchewan Saskatoon Saskatchewan S7N 5E2 Canada.
Nanoscale Adv. 2020 Sep 30;2(10):4938-4950. doi: 10.1039/d0na00643b. eCollection 2020 Oct 13.
The biotic or abiotic reduction of nano-crystalline 2-line ferrihydrite (2-line FH) into more thermodynamically stable phases such as lepidocrocite-LP, goethite-GT, magnetite-MG, and hematite-HT plays an important role in the geochemical cycling of elements and nutrients in aqueous systems. In our study, we employed the use of liquid cell (LC) and semi analysis in an environmental TEM to gain further insights at the micro/nano-scale into the reaction mechanisms by which Fe(ii) catalyzes 2-line FH. We visually observed for the first time the following intermediate steps: (1) formation of round and wire-shaped precursor nano-particles arising only from Fe(ii), (2) two distinct dissolution mechanisms for 2 line-FH ( reduction of size and density as well as breakage through smaller nano-particles), (3) lack of complete dissolution of 2-line FH ( "induction-period"), (4) an amorphous phase growth ("reactive-FH/labile Fe(iii) phase") on 2 line-FH, (5) deposition of amorphous nano-particles on the surface of 2 line-FH and (6) assemblage of elongated crystalline lamellae to form tabular LP crystals. Furthermore, we observed phenomena consistent with the movement of adsorbate ions from solution onto the surface of a Fe(iii)-oxy/hydroxide crystal. Thus our work here reveals that the catalytic transformation of 2-line FH by Fe(ii) at the micro/nano scale doesn't simply occur dissolution-reprecipitation or surface nucleation-solid state conversion mechanisms. Rather, as we demonstrate here, it is an intricate chemical process that goes through a series of intermediate steps not visible through conventional lab or synchrotron bulk techniques. However, such intermediate steps may affect the environmental fate, bioavailability, and transport of elements of such nano-particles in aqueous environments.
纳米晶二线水铁矿(2线FH)在生物或非生物作用下还原为更具热力学稳定性的相,如纤铁矿-LP、针铁矿-GT、磁铁矿-MG和赤铁矿-HT,这在水相系统中元素和养分的地球化学循环中起着重要作用。在我们的研究中,我们利用环境透射电子显微镜中的液体池(LC)和半分析方法,在微观/纳米尺度上进一步深入了解Fe(ii)催化2线FH的反应机制。我们首次直观地观察到以下中间步骤:(1)仅由Fe(ii)形成的圆形和线状前驱体纳米颗粒;(2)2线FH的两种不同溶解机制(尺寸和密度减小以及通过较小纳米颗粒破碎);(3)2线FH缺乏完全溶解(“诱导期”);(4)2线FH上的非晶相生长(“反应性FH/不稳定Fe(iii)相”);(5)非晶纳米颗粒沉积在2线FH表面;(6)细长的结晶薄片组装形成板状LP晶体。此外,我们观察到与吸附质离子从溶液移动到Fe(iii)-氧/氢氧化物晶体表面一致的现象。因此,我们的工作表明,Fe(ii)在微观/纳米尺度上对2线FH的催化转化并非简单地通过溶解-再沉淀或表面成核-固态转化机制发生。相反,正如我们在此所证明的,这是一个复杂的化学过程,经历了一系列传统实验室或同步加速器体相技术无法看到的中间步骤。然而,这些中间步骤可能会影响此类纳米颗粒在水环境中的环境归宿、生物有效性和元素迁移。