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Sorption of Cr(III) and Cr(VI) to High and Low Pressure Synthetic Nano-Magnetite (Fe3O4)Particles

机译:Cr(III)和Cr(VI)对高低压合成纳米磁铁矿(Fe3O4)颗粒的吸附

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摘要

The binding of Cr(III) and Cr(VI) to synthetic nano-magnetie particles synthesized under open vessel conditions and a microwave assisted hydrothermal synthesis techniques was investigated. Batch studies showed that the binding of both the Cr(III) and Cr(VI) bound to the nano-materials in a pH dependent manner. The Cr(III) maximized at binding at pH 4 and 100% binding. Similarly, the Cr(VI) ions showed a maximum binding of 100% at pH 4. The data from the time dependency studies showed for the most part the majority of the binding occurred within the first 5 minutes of contact with the nanomaterial and remained constant thereafter. In addition, the effects of the possible interferences were investigated which showed some effects on the binding of both Cr(III) and Cr(VI). However, the interferences never completely eliminated the chromium binding. Isotherm studies conducted at room temperature showed the microwave synthesized nanomaterials had a binding capacity of 1208 ± 43.9 mg/g and 555 ± 10.5 mg/g for Cr(VI) and Cr(III), respectively. However, the microwave assisted synthesized nanomaterials had capacities of 1705 ± 14.5 and 555± 10.5 mg/g for Cr(VI) and Cr(III), respectively. XANES studies showed the Cr(VI) was reduced to Cr(III), and the Cr(III) remained as Cr(III). In addition, the XANES studies indicated that the chromium remained coordinated in an octahedral arrangement of oxygen atoms.
机译:研究了Cr(III)和Cr(VI)与在开放容器条件下合成的纳米磁性粒子的结合以及微波辅助水热合成技术。批处理研究表明,Cr(III)和Cr(VI)的结合均以pH依赖的方式与纳米材料结合。 Cr(III)在pH 4和100%结合时最大。同样,Cr(VI)离子在pH 4时显示最大结合率为100%。时间依赖性研究的数据显示,大部分结合发生在与纳米材料接触的前5分钟内,并且保持恒定之后。此外,研究了可能的干扰的影响,这些影响显示出对Cr(III)和Cr(VI)结合的某些影响。但是,这些干扰永远不会完全消除铬的结合。在室温下进行的等温研究表明,微波合成的纳米材料对Cr(VI)和Cr(III)的结合能力分别为1208±43.9 mg / g和555±10.5 mg / g。然而,微波辅助合成的纳米材料对Cr(VI)和Cr(III)的容量分别为1705±14.5和555±10.5 mg / g。 XANES研究表明,Cr(VI)还原为Cr(III),而Cr(III)仍为Cr(III)。另外,XANES研究表明铬在氧原子的八面体排列中保持配位。

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