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Thermodynamic evaluation of water splitting by a cation- excessive (Ni, Mn) Ferrite

机译:阳离子过多(Ni,Mn)铁氧体分解水的热力学评估

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摘要

Water-splitting potential by cation-excessive (Ni, Mn) ferrite, Ni_0.5(1+ε) Mn 0.50 (1+ε) Fe 1.99 (1+ε) O_4 was evaluated using he standard Gibbs free energy change (ΔG°) for the cation-excessive ferrite formation in different O_2 partial pressures. The cation-excessive degree betweenε ranged from 0.026 to 0.16 in pO_2 values of 7.9 × 10~-7 to 1.0 × 10~-1. From the relation between ε value of (Ni, Mn) ferrite and oxygen partial pressure, equilibrium constant K (th) was determined. Furthermore ΔH°s for O_2 releasing and water-splitting reactions with cation-excessive (Ni, Mn) ferrite were evaluated From the van't Hoff plot and compared with that for magnetite-wustite system; where ΔH°s were assumed to be the Same values for both (Ni, Mn) ferrite and magnetite-Wustite system: + 300 kJ for O_2 releasing and -35 - -63 kJ For water-splitting.
机译:使用标准吉布斯自由能变化(ΔG°)评估了阳离子(Ni,Mn)铁氧体过多的Ni_0.5(1 +ε)Mn 0.50(1 +ε)Fe 1.99(1 +ε)O_4的水分解势),以在不同的O_2分压下形成过量的阳离子。在7.9×10〜-7至1.0×10〜-1的pO_2值之间,阳离子过量度在ε范围从0.026至0.16。根据(Ni,Mn)铁素体的ε值与氧分压的关系,求出平衡常数K(th)。此外,根据范特霍夫曲线评估了与过量阳离子(Ni,Mn)铁氧体的O_2释放和水分解反应的ΔH°s,并将其与磁铁矿-铁锰矿体系的ΔH°s进行了比较。其中,对于(Ni,Mn)铁氧体和磁铁矿-维氏体系统,ΔH°s假定为相同值:对于O_2释放,+ 300 kJ;对于水分解,-35--63 kJ。

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