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
2014年
10期
3372-3377
,共6页
刘水石%郭宇峰%邱冠周%姜涛%陈凤
劉水石%郭宇峰%邱冠週%薑濤%陳鳳
류수석%곽우봉%구관주%강도%진봉
钒钛磁铁矿%固态还原%还原动力学%还原过程
釩鈦磁鐵礦%固態還原%還原動力學%還原過程
범태자철광%고태환원%환원동역학%환원과정
vanadium-titanium magnetite%solid-state reduction%reduction kinetics%reduction process
研究预氧化钒钛磁铁精矿固态还原反应的动力学,采用XRD、SEM和EDS等手段研究还原产物的显微结构和物相变化,在此基础上,对其固态还原机理进行研究。结果表明:以煤为还原剂,在还原温度为950~1100°C时,预氧化钒钛磁铁精矿的固态还原受界面化学反应控制,反应的表观活化能为67.719 kJ/mol;预氧化钒钛磁铁精矿的还原历程可描述为:预氧化钒钛磁铁精矿→钛铁晶石→钛铁矿→亚铁板钛矿(FeTi2O5)→(FenTi1-n)Ti2O5。预氧化钒钛磁铁精矿在1050°C还原60 min后,还原产物中会形成M3O5型(M为Fe、Ti、Mg、Mn等)固溶体,存在于M3O5固溶体中铁的难还原性是限制预氧化钒钛磁铁矿还原的主要原因。
研究預氧化釩鈦磁鐵精礦固態還原反應的動力學,採用XRD、SEM和EDS等手段研究還原產物的顯微結構和物相變化,在此基礎上,對其固態還原機理進行研究。結果錶明:以煤為還原劑,在還原溫度為950~1100°C時,預氧化釩鈦磁鐵精礦的固態還原受界麵化學反應控製,反應的錶觀活化能為67.719 kJ/mol;預氧化釩鈦磁鐵精礦的還原歷程可描述為:預氧化釩鈦磁鐵精礦→鈦鐵晶石→鈦鐵礦→亞鐵闆鈦礦(FeTi2O5)→(FenTi1-n)Ti2O5。預氧化釩鈦磁鐵精礦在1050°C還原60 min後,還原產物中會形成M3O5型(M為Fe、Ti、Mg、Mn等)固溶體,存在于M3O5固溶體中鐵的難還原性是限製預氧化釩鈦磁鐵礦還原的主要原因。
연구예양화범태자철정광고태환원반응적동역학,채용XRD、SEM화EDS등수단연구환원산물적현미결구화물상변화,재차기출상,대기고태환원궤리진행연구。결과표명:이매위환원제,재환원온도위950~1100°C시,예양화범태자철정광적고태환원수계면화학반응공제,반응적표관활화능위67.719 kJ/mol;예양화범태자철정광적환원역정가묘술위:예양화범태자철정광→태철정석→태철광→아철판태광(FeTi2O5)→(FenTi1-n)Ti2O5。예양화범태자철정광재1050°C환원60 min후,환원산물중회형성M3O5형(M위Fe、Ti、Mg、Mn등)고용체,존재우M3O5고용체중철적난환원성시한제예양화범태자철광환원적주요원인。
The solid-state reduction kinetics of pre-oxidized vanadium-titanium magnetite concentrate was studied. The phase and microstructure of the reduction product were characterized by XRD, SEM and EDS methods, based on which the mechanism of the solid-state reduction was investigated. The results showed that using coal as reductant at 950-1100 °C, the solid-state reduction of the pre-oxidized vanadium-titanium magnetite concentrate was controlled by interface chemical reaction and the apparent activation energy was 67.719 kJ/mol. The mineral phase transformation during the reduction process can be described as follows: pre-oxidized vanadium-titanium magnetite concentrate→ ulvospinel→ ilmenite→ FeTi2O5→ (FenTi1-n)Ti2O5. M3O5-type (M can be Fe, Ti, Mg, Mn, etc) solid solutions would be formed during the reduction process of the pre-oxidized vanadium-titanium magnetite concentrate at 1050 °C for 60 min. The poor reducibility of iron in M3O5solid solutions is the main reason to limit the reduction property of pre-oxidized vanadium-titanium magnetite concentrate.