Possibilities for speciation of Al-citrate and other negatively charged Al complexes by anion-exchange FPLC-ICP-AES

被引:32
作者
Bantan, T
Milacic, R
Pihlar, B
机构
[1] Jozef Stefan Inst, Dept Environm Sci, Ljubljana 1000, Slovenia
[2] Univ Ljubljana, Fac Chem & Chem Technol, Ljubljana 1000, Slovenia
关键词
speciation of Al; separation of Al-citrate; Al-EDTA; Al-oxalate; anion-exchange FPLC-ICP-AES;
D O I
10.1016/S0039-9140(97)00282-8
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An anion-exchange fast protein liquid chromatographic-inductively coupled plasma atomic emission spectrometric procedure (FPLC-ICP-AES) was developed for speciation of Al-citrate and other negatively charged Al complexes. FPLC separations were carried out on a Mono Q HR 5/5 strong anion-exchange FPLC column over a pH range from 3.5 to 11.0. An aqueous-NaNO3 (4 mol dm(-3)) linear gradient elution was applied over 10 min for separation of a particular Al species. The separated Al species were determined in 0.5 cm(3) eluate fractions 'off line' by ICP-AES. Under optimal analytical procedures Al-citrate was separated from Al-oxalate and AI-EDTA in a neutral pH range. Good reproducibility of the FPLC-ICP-AES procedure was obtained for determination of a particular Al species al optimal measurement conditions (RSD +/- 2%). Al3+ and neutral Al-citrate species were strongly adsorbed on the column resin and did not interfere with the separation of negatively charged Al complexes. Al(OH)(4)(-) species were separated from Al-citrate in an alkaline pH region, but quantitatively determined only at a pH of 11.0. The distribution of Al species over a pH range from 3.5 to 11.0 agreed with the reported calculated data. The limit of detection (3 sigma basis) for separated Al species was 0.1 mu g cm(-3). (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:227 / 235
页数:9
相关论文
共 35 条
[1]   ALUMINUM SPECIATION IN AQUEOUS-SOLUTIONS [J].
ACHILLI, M ;
CICERI, G ;
FERRAROLI, R ;
CULIVICCHI, G ;
PIERI, S .
WATER AIR AND SOIL POLLUTION, 1991, 57-8 :139-148
[2]  
ALFREY AC, 1996, J TOXICOL ENV HLTH, V48, P527
[3]   SPECIATION OF ALUMINUM IN AQUEOUS-SOLUTIONS USING ION CHROMATOGRAPHY [J].
BERTSCH, PM ;
ANDERSON, MA .
ANALYTICAL CHEMISTRY, 1989, 61 (06) :535-539
[4]  
CAMPBELL PGC, 1984, VERH INT VER THEOR A, V22, P371
[5]  
CARY EE, 1975, J AGR FOOD CHEM, V23, P23
[6]   THE DETERMINATION OF QUICKLY REACTING ALUMINUM IN NATURAL-WATERS BY KINETIC DISCRIMINATION IN A FLOW SYSTEM [J].
CLARKE, N ;
DANIELSSON, LG ;
SPAREN, A .
INTERNATIONAL JOURNAL OF ENVIRONMENTAL ANALYTICAL CHEMISTRY, 1992, 48 (02) :77-100
[7]   SPECIATION OF ALUMINUM IN SURFACE-WATER [J].
COURTIJN, E ;
VANDECASTEELE, C ;
DAMS, R .
SCIENCE OF THE TOTAL ENVIRONMENT, 1990, 90 :191-202
[8]  
DATTA AK, 1990, J TRACE ELEM ELECT H, V4, P107
[9]   HPLC-AAS HYBRID TECHNIQUE FOR STUDYING THE SPECIATION OF TRACE-METALS (AL, FE, SI, HG) IN BIOLOGICAL-FLUIDS - A REVIEW OF APPLICATIONS, RECENT EXPERIENCES AND PERSPECTIVES [J].
DHAESE, PC ;
VANLANDEGHEM, GF ;
LAMBERTS, LV ;
DEBROE, ME .
MIKROCHIMICA ACTA, 1995, 120 (1-4) :83-90