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Influence of alkaline earth metal cations on the charge transfer kinetics for the redox couple Ti(IV)/Ti(III) in a chloride–fluoride melt

机译:碱土金属阳离子对氯化钠熔体氧化还原Ti(IV)/ Ti(III)的电荷转移动力学的影响

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Abstract The influence of strongly polarizing cations Mg2+, Ca2+, Sr2+, and Ba2+ on the charge transfer kinetics of the redox couple Ti(IV)/Ti(III) is studied. The standard rate constants of charge transfer (k s) for the Ti(IV)/Ti(III) redox couple in the (NaCl–KCl)eq–NaF (10 wt %)–K2TiF6 melt upon the addition of the strongly polarizing cations into the starting melt are determined. The dependence of the charge transfer rate constants on the ionic potential of the cations is established. The activation energies of the charge transfer process are calculated for the fluoride complexes of the Ti(IV)/Ti(III) redox couple with the outer-sphere cations Mg2+, Ca2+, Sr2+, and Ba2+.]]>
机译:<![cdata [<标题>抽象 ara>强偏振阳离子mg 2 + ,ca 2 + ,sr 2+研究了雷诺克耦合Ti(IV)/ Ti(III)的电荷转移动力学上的,和BA <上标> 2 + 。电荷转移的标准速率常数(<强调类型=“斜体”> k <下标> s )(nacl-kcl)中的redox耦合<下标> eq -naf(10wt%) - k <下标> 2 tif <下标> 6 在将强偏振阳离子加入起始熔体时熔体。建立电荷转移率常数对阳离子的离子潜力的依赖性。计算电荷转移过程的激活能量用于Ti(IV)/ Ti(III)氧化还原与外球阳离子Mg <上标> 2 + ,CA <上标> 2+的氟化物复合物,sr 2 + ,ba 2 + ]>

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