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利用对三溴偶氮胂-锆(Ⅳ)络合物的置换反应光度法测定草酸
          
Photometric Determination of Oxalic Acid by Its Displacement Reaction with the Complex of Tribromoarsenazo and Zirconium(Ⅳ)

摘    要
在0.20 mol·L-1盐酸介质中,锆(Ⅳ)与三溴偶氮胂形成1∶1蓝紫色络合物,加入草酸可置换络合物中的三溴偶氮胂,使显色溶液的吸光度升高,草酸的浓度与吸光度升高值成正比.在506 nm波长处,草酸浓度在1.0×10-4~6.5×10-4mol·L-1范围内遵守比耳定律.方法的表观摩尔吸光率ε506 nm=1.23×103L·mol-1·cm-1,检出限为0.074 mg· L-1.方法已直接用于地下水以及西红柿样品中草酸含量的测定,所得结果与文献<参考文献原文>的方法结果相符.测定值的相对标准偏差(n=13)均小于2%,所测得的回收率在95.7%~103.9%之间.
标    签 光度法   草酸   锆(Ⅳ)   三溴偶氮胂   水样   西红柿   Photometry   Oxalic acid   Zirconium(Ⅳ)   Tribromoarsenazo   Ground water   Tomato  
 
Abstract
It was found that the absorbance of the blue-purple complex formed by tribromoarsenazo (AsA-TB) and zirconium(Ⅳ) in 0.20 mol·L-1 HCl medium was increased upon the addition of definite amount of oxalic acid as measured at 506 nm.An equivalent amount of AsA-TB was displaced from the Zr(Ⅳ)-AsA-TB complex by oxalic acid in forming a more stable and colorless complex between Zr(Ⅳ) and oxalic acid,and the absorbance of the test solution was increased due to the increase in concentration of free AsA-TB,which was liberated in the displacement reaction.Beer′s law was kept in the range of 1.0×10-4 to 6.5×10-4mol·L-1.Molar absorptivity of this method was found as 1.23×103L·mol-1·cm-1.Detection limit found was 0.074 mg·L-1.The proposed method has been applied to the determination of oxalic acid in tomato and ground water,giving results in conformity with the results obtained by the method given in literature.Values of RSD′s (n=13) obtained were less than 2%,and values of recovery were in the range of 95.7% to 103.9%.

中图分类号 O657.31

 
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收稿日期 2006/12/19

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备注胡伟华(1964-),男,吉林长春市人,副教授,主要从事分光光度分析.

引用该论文: HU Wei-hua,ZHAI Qing-zhou,WANG Xin-ying. Photometric Determination of Oxalic Acid by Its Displacement Reaction with the Complex of Tribromoarsenazo and Zirconium(Ⅳ)[J]. Physical Testing and Chemical Analysis part B:Chemical Analysis, 2008, 44(4): 352~354
胡伟华,翟庆洲,王馨莹. 利用对三溴偶氮胂-锆(Ⅳ)络合物的置换反应光度法测定草酸[J]. 理化检验-化学分册, 2008, 44(4): 352~354


被引情况:


【1】叶存玲,王治科,冯素玲, "流动注射-催化光度法测定痕量草酸根",理化检验-化学分册 47, 963-965(2011)



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参考文献
【1】Salinas F,Martinez V J,Gonzalez M V.Extraction-spectrophotometric determination of oxalate in urine and blood serum[J].Analyst,1989,114(12):1685.
 
【2】Hatch M.Spectrophotometric determination of oxalate in whole blood[J].Clin Chim Acta,1990,193:199.
 
【3】Paula M L,Robert R L,Timothy S L,et al.Sensitive spectrophotometric assay for plasma oxalate[J].Clin Chem,2005,51:2377.
 
【4】Ensafi A A.Kinetic spectrophotometric method for the determination of oxalic acid by its catalytic effect on the oxidation of safranine by dichromate[J].Spectrochim Acta Part A,2001,57(9):1833.
 
【5】Yan Z Y,Xing G M,Li Z X.Quantitative determination of oxalic acid using victoria blue B based on a catalytic kinetic spectrophotometric method[J].Microchim Acta,2004,144(1/3):199.
 
【6】Chamjangal M A,Keley V,Bagherian G.Kinetic spectrophotometric method for determination of trace amounts of oxalate by an activation effect[J].Anal Sci,2006,22:333.
 
【7】Zhai Q Z.Catalytic kinetic spectrophotometry for the determination of trace amount of oxalic acid in biolocal samples with oxalic acid-rhodamin B-potassium dichromate system[J].Spectrochim Acta Part A,2006,65(1):1.
 
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