Pourbaix图
摩尔浓度
钴
巴(单位)
化学
脱水
热力学
分压
图表
大气温度范围
无机化学
分析化学(期刊)
物理化学
水溶液
有机化学
电化学
氧气
数学
气象学
物理
统计
生物化学
电极
出处
期刊:ChemPlusChem
[Wiley-VCH]
日期:1997-01-01
卷期号:62 (11): 1663-1676
被引量:2
摘要
Diagrams E r - m KOH for cobalt were calculated in the range of molality m KOH = 2-18 mol kg -1 , temperature t = 25-125 °C and total pressure P = 1-30 bar (0.1-3.0 MPa) on the basis of recent reliable data for individual reaction components. The water activity a H 2 O , the equilibrium pressure of the water vapour p H 2 O in or above the KOH solutions was considered. The results displayed differences from the original E -pH diagram for cobalt after Pourbaix. The direct oxidation of Co 3 O 4 to CoO 2 without any intermediate stage of Co(III) oxo compounds was found to be thermodynamically more favourable. Consideration of the reduced water activity in concentrated KOH solutions led to the finding that solid Co(OH) 2 can be dehydrated to CoO at elevated temperatures in contact with KOH solutions. With rising temperature, dehydration can occur at lower KOH molality. CoO 2 , not known in a pure form, was assumed to exist as a pure substance in mixtures with other solid Co oxo compounds in lower states of oxidation.
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