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2010, 03, v.29;No.115 171-175
从钒浸出液中沉淀结晶型钒酸铁试验研究
基金项目(Foundation): 攀钢集团攀枝花钢钒公司科技项目资助(08Y0705)
邮箱(Email):
DOI: 10.13355/j.cnki.sfyj.2010.03.007
摘要:

研究了常压下向钒浸出液中加入硫酸铁沉淀结晶型Fe4(VO4)4.5H2O,考察了温度、pH和添加剂C对沉淀产物钒酸铁的影响。对沉淀产物进行X-射线衍射(XRD)分析和电子扫描电镜观察,结果表明:沉淀产物的n(V)/n(Fe)和钒沉淀率随pH和温度的升高而下降;加入添加剂C有利于钒酸铁的结晶,同时提高产物的n(V)/n(Fe)和钒沉淀率;最佳沉淀条件为:pH为23,反应温度90℃,反应时间72 h,加入添加剂C,此条件下,沉淀产物为Fe4(VO4)4.5H2O,n(V)/n(Fe)接近于1,粒度尺寸主要分布在5~15μm范围内,钒沉淀率在97%以上,。

Abstract:

The crystalline Fe4(VO4)4 5H2O was precipitated at normal pressure from mixing vanadium leaching solution using Fe2(SO4)3.The effects of reaction temperature,pH and additive C on n(V)/n(Fe) of precipitate and vanadium precipitation ratio were investigated.The precipitate was characterized by X-ray diffraction(XRD) and observed by scanning electron microscope(SEM).The results showed that precipitate n(V)/n(Fe) and vanadium precipitation ratio decreased with increasing of pH and reaction temperature.Additive C can increase n(V)/n(Fe) and vanadium precipitation ratio.The best conditions obtained were reaction temperature of 90 ℃,pH of 23,reaction time of 72 h and existence of additive C.Under the conditions,n(V)/n(Fe) of precipitate was close to 1,vanadium precipitation ratio was over 97%,precipitate was conformed as crystalline Fe4(VO4)4·5H2O and grain size of 5~15 μm.

参考文献

[1]Mangamma G,Prabhu E,Gnanasekaran T.Investigationson FeVO4as A Gas Sensor Material[J].Bulletin of Electro-chemistry,1996,12(11/12):696-699.

[2]Poizot P,Baudrin E,Laruelle S,et al.Low Temperature Syn-thesis and Electrochemical Performance of Cristalized FeVO4.1.1H2O[J].Solid State Ionics,2000,138(1/2):31-40.

[3]Deng J H,Jiang J Y,Zhang Y Y,et al.FeVO4as A HighlyActive Heterogeneous Fenton-like Catalyst Towards theDegradation of Orange II[J].Applied Catalysis B:Environ-mental,2008,84(3/4):468-473.

[4]Klissurski D,Iordanova R,Radev D,et al.Mechanochemi-cally Assisted Synthesis of FeVO4Catalysts[J].Journal ofMaterials Science,2004,39(16/17):5375-5377.

[5]廖世明,柏谈.国外钒冶金[M].北京:冶金工业出版社,1985.

[6]Klissurski D,Radev D,Iordanova R,et al.Synthesis of Iron(Ⅲ)Vanadate From Mechanically Activated Precursors[J].Chemic Inorganique,2003,56(6):27-30.

[7]郭振中.提钒工艺综述[J].青海科技情报,1990(3):33-35.

[8]Robertson B,Kostiner E.Crystal Structure and Moss BauerEffect Investigation of FeVO4[J].Journal of Solid StateChemistry,1972,4(1):29-37.

[9]张百川.论从工业溶液中沉淀析出钒的方法[J].钒钛,1989(6):6-10.

[10]Melghit K,Al-Mungi A S.New Form of Iron Orthovana-date FeVO4.1.5H2O Prepared at Normal Pressure andLow Temprerature[J].Materials Science and Engineer-ing:B,2007,136(2/3):177-181.

[11]Poizot P,Laruelle S,Touboul M,et al.Synthesis and CrystalStructure of A New Hydrated Iron(III)Vanadate Fe2(H2O)[V2O7.VO3(OH)][J].J Mater Chem,2000,10(8):1841-1845.

[12]Naeem A,Westerhoff P,Mustafa S.Vanadium Removalby Metal(hydr)oxide Adsorbents[J].Water Research,2007,41(7):1596-1602.

[13]Peacock C L,Sherman D M.Vanadium(V)AdsorptionOnto Goethite(-αFeOOH)at pH 1.5 to 12:A SurfaceComplexation Model Based on Ab Initio Molecular Geome-tries and EXAFS Spectroscopy[J].Geochimica et Cosmo-chimica Acta,2004,68(8):1723-1733.

基本信息:

DOI:10.13355/j.cnki.sfyj.2010.03.007

中图分类号:TF803.2

引用信息:

[1]陈亮.从钒浸出液中沉淀结晶型钒酸铁试验研究[J].湿法冶金,2010,29(03):171-175.DOI:10.13355/j.cnki.sfyj.2010.03.007.

基金信息:

攀钢集团攀枝花钢钒公司科技项目资助(08Y0705)

发布时间:

2010-09-15

出版时间:

2010-09-15

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