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Ternary uranium(VI) carbonato humate complex studied by cryo-TRLFS

机译:低温TRLFS研究三元铀碳酸盐腐殖酸盐配合物

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摘要

The complex formation of U(VI) with humic acid (H ) in the presence of carbonate was studied by time-resolved laser-induced fluorescence spectroscopy at low temperature (cryo-TRLFS) at pH 8.5. In the presence of HA, a decrease of the luminescence intensity of U(VI) and no shift of the emission band maxima in comparison to the luminescence spectrum of the UO_2(CO_3)_3~4- complex, the dominating U(VI) species under the applied experimental conditions in the absence of HA, was observed. The formation of a ternary U(VI) carbonato humate complex of the type UO_2(CO_3)_2HA(II)~4- starting from UO_2(CO_3)_3 ~4- was concluded from the luminescence data. For this complex a complex stability constant of log K = 2.83±0.17 was determined. Slope analysis resulted in a slope of 1.12±0.11, which verifies the postulated complexation reaction. The results agree very well with literature data. Speciation calculations show that the formation of the ternary U(VI) carbonato humate complex can significantly influence the U(VI) speciation under environmental conditions.
机译:通过时间分辨的激光诱导的荧光光谱在低温下(cryo-TRLFS)在pH 8.5下研究了碳酸盐存在下U(VI)与腐殖酸(H)的复杂形成。与HAO_2(CO_3)_3〜4-配合物(主要的U(VI)物种)的发光光谱相比,在HA存在下,U(VI)的发光强度降低,发射带最大值没有移动在没有HA的情况下,在所应用的实验条件下观察到。从发光数据推断出从UO_2(CO_3)_3〜4-开始的UO_2(CO_3)_2HA(II)〜4-型三元U(VI)碳酸盐腐植酸盐复合物的形成。对于该配合物,确定了log K = 2.83±0.17的配合物稳定常数。斜率分析得到的斜率为1.12±0.11,这证实了假定的络合反应。结果与文献数据非常吻合。形态计算表明,三元U(VI)碳酸盐腐殖酸盐复合物的形成可以在环境条件下显着影响U(VI)的形态。

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