中国有色金属学报(英文版)
中國有色金屬學報(英文版)
중국유색금속학보(영문판)
TRANSACTIONS OF NONFERROUS METALS SOCIETY OF CHINA
2011年
3期
566-572
,共7页
刘建元%李志友%陶玉强%张斗%周科朝
劉建元%李誌友%陶玉彊%張鬥%週科朝
류건원%리지우%도옥강%장두%주과조
惰性阳极%尖晶石%相转变%铝电解
惰性暘極%尖晶石%相轉變%鋁電解
타성양겁%첨정석%상전변%려전해
inert anode%spinel%phase transformation%aluminum electrolysis
采用冷压气氛烧结制备17(Cu-10Ni)-(NiFe2O4-10NiO)金属陶瓷,并作为阳极在960℃下分别进行10和40 h的铝电解试验.对电解前后金属陶瓷的显微结构、物相成分进行分析检测.对电解质及阴极金属中的杂质含量进行分析,研究阳极组成中Fe、Ni和Cu元素的腐蚀行为.研究发现:在电解过程中,在材料表面形成NiFe2O4相致密层,该致密层随电解时间的延长而增厚.在NiFe2O4相致密层形成与增厚过程中,出现NiFe2O4相吞噬NiO相和金属相氧化的现象,金属陶瓷中Cu元素优先腐蚀溶解.并着重讨论NiFe2O4相致密层形成与增厚过程中金属相的腐蚀形式及NiO相向NiFe2O4相的转变机制.
採用冷壓氣氛燒結製備17(Cu-10Ni)-(NiFe2O4-10NiO)金屬陶瓷,併作為暘極在960℃下分彆進行10和40 h的鋁電解試驗.對電解前後金屬陶瓷的顯微結構、物相成分進行分析檢測.對電解質及陰極金屬中的雜質含量進行分析,研究暘極組成中Fe、Ni和Cu元素的腐蝕行為.研究髮現:在電解過程中,在材料錶麵形成NiFe2O4相緻密層,該緻密層隨電解時間的延長而增厚.在NiFe2O4相緻密層形成與增厚過程中,齣現NiFe2O4相吞噬NiO相和金屬相氧化的現象,金屬陶瓷中Cu元素優先腐蝕溶解.併著重討論NiFe2O4相緻密層形成與增厚過程中金屬相的腐蝕形式及NiO相嚮NiFe2O4相的轉變機製.
채용냉압기분소결제비17(Cu-10Ni)-(NiFe2O4-10NiO)금속도자,병작위양겁재960℃하분별진행10화40 h적려전해시험.대전해전후금속도자적현미결구、물상성분진행분석검측.대전해질급음겁금속중적잡질함량진행분석,연구양겁조성중Fe、Ni화Cu원소적부식행위.연구발현:재전해과정중,재재료표면형성NiFe2O4상치밀층,해치밀층수전해시간적연장이증후.재NiFe2O4상치밀층형성여증후과정중,출현NiFe2O4상탄서NiO상화금속상양화적현상,금속도자중Cu원소우선부식용해.병착중토론NiFe2O4상치밀층형성여증후과정중금속상적부식형식급NiO상향NiFe2O4상적전변궤제.
17(Cu-10Ni)-(NiFe2O4-10NiO) cermets were prepared by cold pressing and sintering in nitrogen atmosphere,and tested as inert anode for aluminum electrolysis at 960 ℃ for 10 and 40 h,respectively. Microstructures and phase compositions of the as-sintered and post-electrolyzed samples were investigated. The impurity contents in the electrolyte and the cathode metal were detected in order to investigate the corrosion characteristic of the elements ofFe,Ni and Cu in the anode. A dense NiFe2O4 layer was observed on the surface of anode and thickened with prolonging the electrolysis time. In the newly formed dense ceramic layer,NiO phase disappeared as a result of being swallowed by NiFe2O4 phase,and the metal phase was oxidized during the electrolysis in which Cu element showed a higher dissolution rate than Fe and Ni elements. The formation process of the dense ceramic layer during the electrolysis was presented and explained by using the corrosion mode of the metal phase and the transformation mechanism from NiO phase to NiFe2O4 phase.