Lefèvre G, Noinville S, Fédoroff M
ENSCP-LECA-CNRS UMR 7575, 11, Rue Pierre et Marie Curie, F-75231 Paris cedex 05, France.
J Colloid Interface Sci. 2006 Apr 15;296(2):608-13. doi: 10.1016/j.jcis.2005.09.016. Epub 2005 Oct 3.
In this paper, we present results of ATR-IR spectroscopy of uranyl complexes adsorbed on hematite. This method allowed the in situ recording of infrared spectra of uranyl sorbed on hematite in presence of aqueous solution and to detect one peak at 906 cm(-1) attributed to the antisymmetric O=U=O stretching. The intensity of the peak increases with pH, but its shape does not evolve, indicating that the same surface species is responsible for the sorption in the pH range 5-8. The reversibility experiments confirm that the hematite deposit reacts in the same way as dispersed suspensions. Measurement of the stretching frequency of nitrate ions coming from electrolyte showed a pure electrostatic adsorption and exclude the formation of a ternary complex with uranyl.
在本文中,我们展示了吸附在赤铁矿上的铀酰配合物的衰减全反射红外光谱(ATR-IR)结果。该方法能够原位记录在水溶液存在下吸附在赤铁矿上的铀酰的红外光谱,并检测到一个位于906 cm⁻¹处的峰,该峰归因于反对称O=U=O伸缩振动。该峰的强度随pH值增加,但形状不变,这表明在pH值为5 - 8的范围内,相同的表面物种负责吸附过程。可逆性实验证实,赤铁矿沉积物的反应方式与分散悬浮液相同。对来自电解质的硝酸根离子伸缩频率的测量表明存在纯静电吸附,排除了与铀酰形成三元配合物的可能性。