Development of a new method for the separation of vanadium species and chloride interference removal using modified silica capillaries-DIN-ICP-MS

被引:19
作者
Garcia-Sanchez, R
Bettmer, J
Ebdon, L
机构
[1] Univ Plymouth, Plymouth Environm Res Ctr, Plymouth PL4 8AA, Devon, England
[2] Univ Mainz, Inst Anorgan & Analyt Chem, D-55099 Mainz, Germany
关键词
vanadium speciation; direct injection nebuliser-inductively coupled plasma-mass spectrometer (DIN-ICP-MS); modified capillaries; on-line separation; spectral interferences;
D O I
10.1016/S0026-265X(03)00158-9
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学]; 081704 [应用化学];
摘要
A new on-line method for the separation of vanadium (IV) and vanadium (V) as well as for the removal of ClO+ mass spectral interference on vanadium determination by quadrupole-ICP-MS has been developed. The sample introduction system consists of a modified fused silica capillary coupled to a direct injection nebuliser (DIN), between the solvent delivery system and the ICP. Fused silica capillaries were treated with different anion and cation exchanger reagents and were tested for the retention of Cl- and the separation of vanadium ions at mug l(-1) levels. A suitable strong anion exchanger functional group (3-aminopropyltrimethoxy silane) was selected. Chlorine anions were retained in this anionic capillary and the separation between V(IV) and V(V) was possible in the pH range 2-4. The selections of instrumental ICP-MS conditions for the minimisation of the ClO+ interference were carefully considered. Factors affecting the chromatographic separation such as sample pH, sample flow rate, effect of methanol in the mobile phase and length of the capillary for the separation were optimised. The proposed methodology provides a simple and rapid method for vanadium speciation. A relative detection limit of 12 l(-1) (i.e. absolute detection limits of 120 pg) for V(IV) based on peak height measurements was obtained. The relative standard deviation for V(IV) was 2.4% for a 10 mul injection (n=6). (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:161 / 171
页数:11
相关论文
共 30 条
[1]
ABBASI SA, 1987, ANAL LETT, V20, P1347
[2]
DETERMINATION OF ARSENIC IN SAMPLES WITH HIGH CHLORIDE CONTENT BY INDUCTIVELY COUPLED PLASMA MASS-SPECTROMETRY [J].
BRANCH, S ;
EBDON, L ;
FORD, M ;
FOULKES, M ;
ONEILL, P .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1991, 6 (02) :151-154
[3]
THE DETERMINATION OF DISSOLVED AND PARTICULATE VANADIUM IN SEA-WATER BY X-RAY-FLUORESCENCE SPECTROMETRY [J].
COLE, PC ;
ECKERT, JM ;
WILLIAMS, KL .
ANALYTICA CHIMICA ACTA, 1983, 153 (OCT) :61-67
[4]
RAPID SEQUENTIAL DETERMINATION OF CHROMIUM(III) - CHROMIUM(VI) BY FLOW-INJECTION ANALYSIS - INDUCTIVELY COUPLED PLASMA ATOMIC-EMISSION SPECTROMETRY [J].
COX, AG ;
COOK, IG ;
MCLEOD, CW .
ANALYST, 1985, 110 (04) :331-333
[5]
SIMPLE APPROACH TO REDUCING POLYATOMIC ION INTERFERENCES ON ARSENIC AND SELENIUM IN INDUCTIVELY COUPLED PLASMA MASS-SPECTROMETRY [J].
EVANS, EH ;
EBDON, L .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1989, 4 (03) :299-300
[6]
On-line removal of mass interferences in palladium determination by ICP-MS using modified capillaries coupled to micro-flow nebulizers [J].
García, R ;
Gómez, M ;
Palacios, MA ;
Bettmer, J ;
Camara, C .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 2001, 16 (05) :481-486
[7]
Lead speciation in rainwater samples by modified fused silica capillaries coupled to a direct injection nebulizer (DIN) for sample introduction in ICP-MS [J].
Garcia-Sanchez, R ;
Feldhaus, R ;
Bettmer, J ;
Ebdon, L .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 2001, 16 (09) :1028-1034
[9]
SIMPLEX OPTIMIZATION OF NITROGEN ARGON PLASMAS IN INDUCTIVELY COUPLED PLASMA MASS-SPECTROMETRY FOR THE REMOVAL OF CHLORIDE-BASED INTERFERENCES [J].
HILL, SJ ;
FORD, MJ ;
EBDON, L .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1992, 7 (05) :719-725
[10]
MUTUAL SEPARATION AND PRECONCENTRATION OF VANADIUM(V) AND VANADIUM(IV) IN NATURAL-WATERS WITH CHELATING FUNCTIONAL-GROUP IMMOBILIZED SILICA-GELS FOLLOWED BY DETERMINATION OF VANADIUM BY INDUCTIVELY COUPLED PLASMA ATOMIC EMISSION-SPECTROMETRY [J].
HIRAYAMA, K ;
KAGEYAMA, S ;
UNOHARA, N .
ANALYST, 1992, 117 (01) :13-17