Electrochemical oxidation of H2S on polycrystalline Ni electrodes

被引:15
作者
Yang, Jian [1 ]
Smulders, Vera [1 ]
Smits, Joost J. T. [2 ]
Mei, Bastian T. [1 ]
Mul, Guido [1 ]
机构
[1] Univ Twente, MESA Inst Nanotechnol, Fac Sci & Technol, PhotoCatalyt Synth Grp, Meander 229,POB 217, NL-7500 AE Enschede, Netherlands
[2] Shell Technol Ctr Amsterdam, POB 38000, NL-1030 BN Amsterdam, Netherlands
关键词
H2S; Ni anode; Sulfide oxidation; Sulfide selectivity; Basic conditions; Phosphate buffer; Anode deactivation; SULFIDE ION; HYDROGEN;
D O I
10.1007/s10800-019-01334-x
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
We have evaluated the applicability of Ni anodes in electrochemical conversion of H2S to form sulfur (polysulfides) and H-2. Two different electrolytes containing sulfide were evaluated: a buffered solution of Na2HPO4 at pH 9.2, and a NaOH solution at pH 13. At pH 9.2, deposition of sulfur on the Ni anode was observed, resulting in a significant decrease in electrochemical performance. The composition, morphology, and thickness of the sulfur deposit, as determined by Raman spectroscopy and SEM, was found to strongly depend on the applied potential, and ranged from dense S-8 films to highly porous spherical sulfur structures. Oxidation of the anode was also observed by conversion of Ni to NiS2. The formation of the sulfur film was prevented by performing the reaction at pH 13 in NaOH in the range of - 1.0 V to + 0.6 V versus Hg/HgO. It is proposed that at these highly basic pH values, sulfur is dissolved in the electrolyte in the form of polysulfides, such as S-2(2-) or S-8(2-). When using Ni anodes some oxygen evolution was observed at the anode, in particular at pH 13, resulting in a Faradaic efficiency for sulfur removal of similar to 90%. Graphic
引用
收藏
页码:929 / 936
页数:8
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