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A Novel Electrochemical Process for Desulfurization in the CaO-SiO2-Al2O3 System

机译:CaO-SiO2-Al2O3体系中新型脱硫电化学方法

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摘要

The effect of electric potential on the sulfide capacity of the CaO-SiO -Al O system was evaluated by applying voltages in the range of −1.5 to 1.5 V at 1823 K in a C/CO gas equilibrium. When the cathodic potential (−1.5 to 0 V) was applied, it was confirmed that the sulfur partition ratio increased based on the electrochemical reaction of sulfur (S + 2e = S ). However, the reversibility of the electrochemical resulfurization reaction (S = S + 2e ) in slag was not established in the reverse (anodic) potential region (0–1.5 V), yet the sulfur partition ratio increased. In particular, sulfur evaporation was observed in the anodic potential region. Therefore, in the present study, potential anodic electro-desulfurization mechanisms based on sulfur evaporation are proposed. To verify these mechanisms, sulfur evaporation is discussed in detail as a function of the thermodynamic stability of sulfur in the slag.
机译:通过在C / CO气体平衡下于1823 K施加-1.5至1.5 V范围内的电压来评估电势对CaO-SiO -Al O系统的硫化容量的影响。当施加阴极电位(-1.5至0V)时,证实基于硫的电化学反应(S + 2e = S),硫分配比增加。但是,在反向(阳极)电势区域(0-1.5 V)中,炉渣中电化学再硫化反应(S = S + 2e)的可逆性尚未建立,但硫的分配比却增加了。特别地,在阳极电位区域中观察到硫蒸发。因此,在本研究中,提出了基于硫蒸发的潜在阳极电脱硫机理。为了验证这些机理,将详细讨论硫的蒸发与炉渣中硫的热力学稳定性的关系。

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