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利用N-正辛基苯胺萃取色谱法从含铝(Ⅲ)混合物中分离铝(Ⅲ)(英文)

Extraction chromatography of aluminium(Ⅲ) and mutual separation of aluminium(Ⅲ) ,gallium(Ⅲ) ,indium(Ⅲ) and thallium(Ⅲ) with N-n-octylaniline
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摘要 A selective method has been developed for the extraction chromatography of aluminium(Ⅲ) and its separation from several metal ions with a chromatographic column containing N-n-octylaniline ( a liquid anion exchanger) coated on silanized silica gel as a stationary phase. The aluminium(Ⅲ) was quantitatively extracted with the 0. 065 mol / L N-n-octylaniline in 0. 013 to 0. 05 mol / L sodium succinate at a flow rate of 1. 0 mL / min. The extracted metal ion has been recovered by eluting with 25. 0 mL of 0. 05 mol / L hydrochloric acid and estimated spectrophotometrically with aurintricarboxylic acid. The effects of the acid concentration,the reagent concentration,the flow rate and the eluting agents have been investigated. The log-log plots of distribution coefficient ( K d ( Al(Ⅲ) ) ) versus N-n-octylaniline concentration in 0. 005 and 0. 007 mol / L sodium succinate gave the slopes of 0. 5 and 0. 7 respectively and showed the probable composition of the extracted species was 1∶ 1 ( metal to amine ratio ) and the nature of extracted species was [RR' NH + 2 Al succinate 2 ] org. . The extraction of aluminium(Ⅲ) was carried out in the presence of various ions to ascertain the tolerance limit of individual ions. Aluminium(Ⅲ) has been separated from multicomponent mixtures,pharmaceutical samples and synthetic mixtures corresponding to alloys. A scheme for mutual separation of aluminium(Ⅲ) ,indium(Ⅲ) ,gallium(Ⅲ) and thallium(Ⅲ) has been developed by using suitable masking agents. The method is fast,accurate and precise. A selective method has been developed for the extraction chromatography of aluminium(Ⅲ) and its separation from several metal ions with a chromatographic column containing N-n-octylaniline ( a liquid anion exchanger) coated on silanized silica gel as a stationary phase. The aluminium(Ⅲ) was quantitatively extracted with the 0. 065 mol / L N-n-octylaniline in 0. 013 to 0. 05 mol / L sodium succinate at a flow rate of 1. 0 mL / min. The extracted metal ion has been recovered by eluting with 25. 0 mL of 0. 05 mol / L hydrochloric acid and estimated spectrophotometrically with aurintricarboxylic acid. The effects of the acid concentration,the reagent concentration,the flow rate and the eluting agents have been investigated. The log-log plots of distribution coefficient ( K d ( Al(Ⅲ) ) ) versus N-n-octylaniline concentration in 0. 005 and 0. 007 mol / L sodium succinate gave the slopes of 0. 5 and 0. 7 respectively and showed the probable composition of the extracted species was 1∶ 1 ( metal to amine ratio ) and the nature of extracted species was [RR' NH + 2 Al succinate 2 ] org. . The extraction of aluminium(Ⅲ) was carried out in the presence of various ions to ascertain the tolerance limit of individual ions. Aluminium(Ⅲ) has been separated from multicomponent mixtures,pharmaceutical samples and synthetic mixtures corresponding to alloys. A scheme for mutual separation of aluminium(Ⅲ) ,indium(Ⅲ) ,gallium(Ⅲ) and thallium(Ⅲ) has been developed by using suitable masking agents. The method is fast,accurate and precise.
出处 《色谱》 CAS CSCD 北大核心 2012年第9期931-937,共7页 Chinese Journal of Chromatography
基金 supported by BCUD,Pune University for providing financial assistance in form of a research project
关键词 extraction chromatography mutual separations aluminium(Ⅲ) indium(Ⅲ) gallium(Ⅲ) thallium(Ⅲ) multicomponent mixtures extraction chromatography mutual separations aluminium(Ⅲ) indium(Ⅲ) gallium(Ⅲ) thallium(Ⅲ) multicomponent mixtures
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  • 1Platinum. [ 2008-02-26 ]. http://en. wikipedia. org/wiki/ Platinum.
  • 2Mhaske A A, Dhadke P M. Hydrometallurgy, 2001, 61 : 143.
  • 3Kwang S C, Chang H L, Yeong J P, et al. Bull Korean Chem Soc, 2001, 22(8) : 801.
  • 4Sunder Raju P V, Merkle R K W, Graser P, et al. Current Science, 2007, 93(5) : 851.
  • 5Rane M V, Venugopal V. Hydrometallurgy, 2006, 84(1/2): 54.
  • 6Preston J S, du Preez A C. Solvent Extr Ion Exch, 2002, 20 (3) : 359.
  • 7Godlewska-Zylkiewicz B, Lesniewska B. J Trace Microprobe Tech, 2001, 19:345.
  • 8Saitoh T, Suzuki S, Hiraide M. J Chromatogr A, 2005, 1097 (1/2) : 179.
  • 9Pyrzynska K. Talanta, 1998, 47:841.
  • 10Elci L, Soylak M, Buyuksekerci E B. Anal Sci, 2003, 19: 1 621.

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