Indirect electrochemical reduction of carbon dioxide to carbon nanopowders in molten alkali carbonates: Process variables and product properties

被引:128
作者
Ijije, Happiness V.
Sun, Chenggong
Chen, George Z. [1 ]
机构
[1] Univ Nottingham, Fac Engn, Dept Chem & Environm Engn, Nottingham NG7 2RD, England
基金
英国工程与自然科学研究理事会;
关键词
PULVERIZED COAL; FLUORIDE MEDIA; ELECTROLYSIS; SALTS; FILMS; CO2; ELECTRODEPOSITION; LICL-KCL-K2CO3; COMBUSTION; OXIDATION;
D O I
10.1016/j.carbon.2014.02.052
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Carbon was deposited on a mild steel cathode during electrolysis in the molten mixture of Li2CO3 and K2CO3 (mole ratio: 62:38) under CO2 or mixed N-2 and CO2 atmospheres at 3.0-5.0 V and 540-700 degrees C. In a three-electrode cell, cyclic voltammetry was applied on a platinum working electrode to study the reduction and deposition processes. A two-electrode cell helped correlate electrolysis variables, e.g. temperature and voltage, with the deposition rate, current efficiency, and properties of the deposited carbon powders. High current efficiency (>90%) and deposition rate (>0.11 g cm(-2) h(-1)) were achieved in the study. Elemental analysis of the electro-deposits, following washing with HCl solutions (2.3-7.8 molL(-1)), showed carbon as the dominant element (75-95 wt.%) plus oxygen (5-10 wt.%) and small amounts of other elements related to materials of the electrolytic cell. Thermogravimetry detected fairly low onset combustion temperatures (310-430 degrees C), depending on the electrolysis and acid washing conditions. Amorphous and various nanostructures (sheet, rings and quasi-spheres) were revealed by electron microscopy in carbon samples deposited under different process conditions. The specific surface area of the carbon deposited at 5.0 V and 540 degrees C was as high as 585 m(2) g(-1). An analysis of the energy consumption suggests several ways for efficiency improvement so that the electrolytic carbon from CO2 will become commercially attractive. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:163 / 174
页数:12
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