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Reduction of antimony by nano-particulate magnetite and mackinawite

机译:纳米微粒磁铁矿和马基诺石还原锑

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The speciation of antimony is strongly influenced by its oxidation state (V, III, 0, -III). Redox processes under anaerobic groundwater conditions may therefore greatly alter the environmental behaviour of Sb. Employing X-ray absorption and photoelectron spectroscopy, we show here that Sb(V) is reduced to Sb(III) by magnetite and mackinawite, two ubiquitous Fe(II)-containing minerals, while Sb(III) is not reduced further. At the surface of magnetite, Sb(III) forms a highly symmetrical sorption complex at the position otherwise occupied by tetrahedral Fe(III). The Sb(V) reduction increases with pH, and at pH values >6.5 Sb(V) is completely reduced to Sb(III) within 30 days. In contrast, at the mackinawite surface, Sb(V) is completely reduced across a wide pH range and within 1 h. The Sb(V) reduction proceeds solely by oxidation of surface Fe(II), while the oxidation state of sulphide is conserved. Independent of whether Sb(V) or Sb(III) was added, an amorphous or nano-particulate SbS_3-like solid formed.
机译:锑的形态受到其氧化态(V,III,0,-III)的强烈影响。因此,在厌氧地下水条件下的氧化还原过程可能会大大改变Sb的环境行为。利用X射线吸收和光电子能谱,我们在这里表明,磁铁矿和马基磁铁矿(两种普遍存在的含Fe(II)的矿物)将Sb(V)还原为Sb(III),而Sb(III)并未进一步还原。在磁铁矿表面,Sb(III)在原本由四面体Fe(III)占据的位置上形成高度对称的吸附络合物。 Sb(V)的减少随pH的增加而增加,并且在pH值> 6.5时,Sb(V)在30天内完全还原为Sb(III)。相比之下,在马基诺石表面,Sb(V)在很宽的pH范围内和1小时内被完全还原。 Sb(V)还原仅通过表面Fe(II)的氧化而进行,而硫化物的氧化态得以保留。不论是否添加Sb(V)或Sb(III),都会形成无定形或纳米微粒状SbS_3状固体。

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