A Fuel-Cell Reactor for the Direct Synthesis of Hydrogen Peroxide Alkaline Solutions from H2 and O2

被引:32
作者
Yamanaka, Ichiro [1 ]
Onisawa, Takeshi [1 ]
Hashimoto, Toshikazu [1 ]
Murayama, Toru [1 ]
机构
[1] Tokyo Inst Technol, Dept Appl Chem, Meguro Ku, Tokyo 1528552, Japan
关键词
electrochemistry; ion-exchange membranes; fuel cells; hydrogen peroxide; CARBON-FIBER; H2O2; CATALYST; CATHODE; SYSTEM;
D O I
10.1002/cssc.201000263
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The effects of the type of fuel-cell reactors (undivided or divided by cation-and anion-exchange membranes), alkaline electrolytes (LiOH, NaOH, KOH), vapor-grown carbon fiber (VGCF) cathode components (additives: none, activated carbon, Valcan XC72, Black Pearls 2000, Seast-6, and Ketjen Black), and the flow rates of anolyte (0, 1.5, 12 mLh(-1)) and catholyte (0, 12 mLh(-1)) on the formation of hydrogen peroxide were studied. A divided fuel-cell system, O-2 (g) jVGCF-XC72 cathode vertical bar 2M NaOH catholyte vertical bar cation-exchange membrane (Nafion-117) vertical bar Pt/XC72-VGCF anode vertical bar 2M NaOH anolyte at 12 mLh(-1) flow vertical bar H-2 (g), was effective for the selective formation of hydrogen peroxide, with 130 mAcm(-2), a 2M aqueous solution of H2O2/NaOH, and a current efficiency of 95% at atmospheric pressure and 298 K. The current and formation rate gradually decreased over a long period of time. The cause of the slow decrease in electrocatalytic performance was revealed and the decrease was stopped by a flow of catholyte. Cyclic voltammetry studies at the VGCF-XC72 electrode indicated that fast diffusion of O-2 from the gas phase to the electrode, and quick desorption of hydrogen peroxide from the electrode to the electrolyte were essential for the efficient formation of solutions of H2O2/NaOH.
引用
收藏
页码:494 / 501
页数:8
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