Intensification of water electrolysis in a centrifugal field

被引:79
作者
Cheng, H [1 ]
Scott, K [1 ]
Ramshaw, C [1 ]
机构
[1] Univ Newcastle Upon Tyne, Dept Chem & Proc Engn, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
关键词
D O I
10.1149/1.1512916
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The intensification of the production of hydrogen and oxygen, i.e., water electrolysis, was achieved in a centrifugal acceleration field. This was demonstrated by measuring the cell voltage and the electrode potentials for cells operated with and without centrifugal fields, as a function of current density. Under industrial electrolysis conditions, greater reductions in cell voltage and in electrode potentials were achieved at a relative acceleration rate of 190 G compared to those in stationary conditions. The relationships between the cell performance and relative acceleration rate, applied G value, for different anode materials, temperature, and NaCl concentration are reported. The data is obtained in acid, neutral, and highly alkaline electrolyte solutions using linear sweep voltammetry, galvanostatic, and potentiostatic polarization techniques. A cell voltage reduction of up to 700 mV, an anode potential reduction of up to 500 mV, and a cathode potential reduction of up to 350 mV at 3 kA m(-2) are achieved at a relative acceleration rate of 190 G and 80degreesC, compared to those in stationary conditions. The saving in cell voltage, and thus energy consumption, are significantly larger than the small amount of energy required to rotate the cells. (C) 2002 The Electrochemical Society.
引用
收藏
页码:D172 / D177
页数:6
相关论文
共 14 条
[1]  
CHENG H, 1999, THESIS U NEWCASTLE U
[2]   THE EFFECT OF TEMPERATURE ON THE WATER ELECTROLYSIS REACTIONS ON NICKEL AND NICKEL-BASED CODEPOSITS [J].
FERREIRA, AC ;
GONZALEZ, ER ;
TICIANELLI, EA ;
AVACA, LA ;
MATVIENKO, B .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1988, 18 (06) :894-898
[3]  
HOGARTH MP, 1995, THESIS NEWCASTLE U N
[4]  
HOOVER TV, 1964, Patent No. 3119759
[5]   POLYMER ELECTROLYTE-TYPE ELECTROCHEMICAL OZONE GENERATOR WITH AN OXYGEN CATHODE [J].
KATOH, M ;
NISHIKI, Y ;
NAKAMATSU, S .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1994, 24 (06) :489-494
[6]  
KINOSHITA K, 1992, ELECTROCHEMICAL OXYG, pCH7
[7]  
LASIA A, 1993, CURRENT TOPICS ELECT, V2, P239
[8]  
PLETCHER D, 1993, IND ELECTROCHEMISTRY, pCH5
[9]   THE OPPORTUNITIES FOR EXPLOITING CENTRIFUGAL FIELDS [J].
RAMSHAW, C .
HEAT RECOVERY SYSTEMS & CHP, 1993, 13 (06) :493-513
[10]   THE ROLE OF ABSORBED HYDROGEN ON THE VOLTAGE-TIME BEHAVIOR OF NICKEL CATHODES IN HYDROGEN EVOLUTION [J].
ROMMAL, HEG ;
MORGAN, PJ .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1988, 135 (02) :343-346