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Kinetic and mechanistic features on the reaction of stored TiO2 electrons with Hg (II), Pb (II) and Ni (II) in aqueous suspension

机译:水性悬浮液中储存的TiO2电子与Hg(II),Pb(II)和Ni(II)反应的动力学和力学特征

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摘要

The reaction of electrons stored on TiO2 nanoparticles with heavy metal ions Hg (II), Ni (II) and Pb (II) has been studied employing steady state and stopped flow spectrophotometric techniques. Prior to kinetic investigation the formation of metal deposits is detected by their surface Plasmon absorbance observed after mixing of their corresponding metal ions with stored electron on TiO2 nanoparticles (eTiO2-). The dynamic of transfer of stored TiO2 electrons to Hg (II), Pb (II) and Ni (II) in water has been investigated after mixing in the stopped flow chamber following the decrease of the absorbance of eTiO2- at 600nm. The results indicate that Hg (II), Pb (II) and Ni (II) ions react readily with eTiO2-The kinetic parameters of the electron transfer reactions have been obtained by pseudo first order fitting. In the presence of Hg (II) ions, the transients decay followed by a buildup at 380-480nmrange. In the presence of Pb (II) and Ni (II), a concurrent decay of TiO2 electron absorbance and buildup of the absorbance of metal deposits were observed. The rate constants of the electron transfer reactions induced by TiO2 stored electrons to metal ions increase with the driving force of the reaction according to Tafel equation.
机译:利用稳态和停止流式分光光度法研究了储存在TiO2纳米颗粒上的电子与重金属离子Hg(II),Ni(II)和Pb(II)的反应。在动力学研究之前,通过将其相应的金属离子与TiO2纳米颗粒(eTiO2-)上存储的电子混合后观察到的表面等离子体吸收来检测金属沉积物的形成。在eTiO2-在600nm处的吸光度降低之后,在停止的流动室中混合后,已经研究了水中储存的TiO2电子向水中Hg(II),Pb(II)和Ni(II)转移的动力学。结果表明,Hg(II),Pb(II)和Ni(II)离子易于与eTiO2-反应。电子转移反应的动力学参数已通过拟一级拟合获得。在存在Hg(II)离子的情况下,瞬态衰减并随后在380-480nm范围内累积。在Pb(II)和Ni(II)的存在下,观察到TiO2电子吸光度同时衰减和金属沉积物吸光度的累积。根据Tafel方程,由TiO2储存的电子引起的电子转移反应的速率常数根据反应的驱动力而增加。

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