Complexation effect of antimony compounds with citric acid and its application to the speciation of antimony(III) and antimony(V) using HPLC-ICP-MS

被引:108
作者
Zheng, J [1 ]
Iijima, A [1 ]
Furuta, N [1 ]
机构
[1] Chuo Univ, Dept Appl Chem, Environm Chem Lab, Bunkyo Ku, Tokyo 1128551, Japan
关键词
D O I
10.1039/b101943k
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this work, a complexation effect of Sb compounds with citric acid was observed using electrospray mass spectrometry (ES-MS). It was found that both Sb(III) and Sb(V) could form complexes readily with citric acid in an aqueous solution at room temperature. These complexes were found to be very stable in various matrices (moat water and aqueous extracts of airborne particulate matter), therefore, a novel HPLC-ICP-MS analytical method for the speciation of Sb(III) and Sb(V) in environmental samples was developed by using the observed complexation effect. Sb(III)- and Sb(V)-citrate complexes were separated on a PRP-X100 anion-exchange column with 10 mmol l(-1) EDTA-1 mmol l(-1) phthalic acid (pH 4.5) as a mobile phase. All complexes were retained on the separation column. and none of them eluted in the solvent front. Low detection limits of 0.05 mug l(-1) and 0.07 mug l(-1) were achieved for Sb(III) and Sb(V), respectively. The calibration curves were linear over the range of 1.0-250 mug l(-1) for the investigated Sb species. The precisions, evaluated by using the relative standard deviation (%RSD) with a 2 mug l(-1) standard solution. were 1.8% and 3.3% for Sb(III) and Sb(V), respectively. Several advantages of the developed method. such as improving chromatographic separation, stabilizing Sb compounds in a water sample, and preventing Sb(III) from oxidizing to Sb(V) during the ultrasonic-assisted and microwave-assisted extraction of an airborne particulate matter (APM) sample using 26 mmol l(-1) citric acid as an extraction solvent. and alleviating the adsorption of Sb compounds on the sample surface, were observed. The developed method enabled us to detect the most toxic Sb specie, Sb(III), in an APM sample for the first time.
引用
收藏
页码:812 / 818
页数:7
相关论文
共 22 条
[1]   DETERMINATION OF DISSOLVED INORGANIC ANTIMONY(V) AND ANTIMONY(III) SPECIES IN NATURAL-WATERS BY HYDRIDE GENERATION ATOMIC-ABSORPTION SPECTROMETRY [J].
APTE, SC ;
HOWARD, AG .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1986, 1 (03) :221-225
[2]   SIMULTANEOUS DETERMINATION OF INORGANIC ARSENIC AND ANTIMONY SPECIES IN NATURAL-WATERS USING SELECTIVE HYDRIDE GENERATION WITH GAS-CHROMATOGRAPHY PHOTOIONIZATION DETECTION [J].
CUTTER, LS ;
CUTTER, GA ;
SANDIEGOMCGLONE, MLC .
ANALYTICAL CHEMISTRY, 1991, 63 (11) :1138-1142
[3]   STABILITY STUDY OF TOTAL ANTIMONY, SB(III) AND SB(V) AT THE TRACE LEVEL [J].
DELACALLEGUNTINAS, MB ;
MADRID, Y ;
CAMARA, C .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 1992, 344 (1-2) :27-29
[4]  
ELINDER DG, 1979, HDB TOXICOLOGY METAL, P283
[5]   Identification and chromatographic separation of antimony species with α-hydroxy acids [J].
Guy, A ;
Jones, P ;
Hill, SJ .
ANALYST, 1998, 123 (07) :1513-1518
[6]   Potential of high performance liquid chromatography coupled to flow injection hydride generation atomic absorption spectrometry for the speciation of inorganic and organic antimony compounds [J].
Krachler, M ;
Emons, H .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 2000, 15 (03) :281-285
[7]   Speciation of antimony for the 21st century: promises and pitfalls [J].
Krachler, M ;
Emons, H ;
Zheng, J .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2001, 20 (02) :79-90
[8]   Urinary antimony speciation by HPLC-ICP-MS [J].
Krachler, M ;
Emons, H .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 2001, 16 (01) :20-25
[9]   Speciation analysis of antimony by high-performance liquid chromatography inductively coupled plasma mass spectrometry using ultrasonic nebulization [J].
Krachler, M ;
Emons, H .
ANALYTICA CHIMICA ACTA, 2001, 429 (01) :125-133
[10]   Simultaneous determination of arsenic, selenium and antimony species using HPLC/ICP-MS [J].
Lindemann, T ;
Prange, A ;
Dannecker, W ;
Neidhart, B .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 1999, 364 (05) :462-466