Determination of Ag, Te, U and Au in waters and in biological samples by FI-TCP-MS following on-line preconcentration

被引:43
作者
Dressler, VL
Pozebon, D
Curtius, AJ
机构
[1] Univ Fed Santa Catarina, Dept Quim, BR-88040900 Florianopolis, SC, Brazil
[2] Univ Fed Santa Maria, Dept Quim, BR-97119900 Santa Maria, RS, Brazil
[3] Univ Fed Rio Grande Sul, Inst Quim, BR-91501970 Porto Alegre, RS, Brazil
关键词
inductively coupled plasma mass spectrometry; flow injection analysis; O; O-diethyl dithiophosphoric acid; biological materials; water; preconcentration;
D O I
10.1016/S0003-2670(01)00861-3
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An on-line preconcentration system for Au, Ag, Te and U, using solenoid valves, a mini-column filled with Cls immobilized on silica to retain the complexes formed with the ammonium salt of O,O-diethyl dithiophosphoric acid and elution with methanol is proposed. All parameters of the preconcentration, such as sample flow rate, concentration of the complexing agent, acid nature acid concentration and elution were optimized. Due to the difficulty of finding compromising conditions for all analytes, they were determined individually. Detections limits ranged from 0.05 to 2.24 pg ml(-1) for U and Te, respectively, while the preconcentration factors ranged from 2.6 to 180 for U and Te, respectively. The precision was adequate for the low measured concentrations, with R.S.D, below 10%. Accuracy was assured by the analysis of standard reference enriched water, sea and riverine waters, milk powder, apple leaves and urine, after microwave-assisted digestion of the last three materials. The relatively small volume of methanol, diluted to 1 + 1, introduced into a conventional nebulizer, minimizes the problems associated with the introduction of organic solvent in the plasma. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:235 / 244
页数:10
相关论文
共 24 条
[1]   SIGNAL ENHANCEMENT OF ELEMENTS DUE TO THE PRESENCE OF CARBON-CONTAINING COMPOUNDS IN INDUCTIVELY COUPLED PLASMA MASS-SPECTROMETRY [J].
ALLAIN, P ;
JAUNAULT, L ;
MAURAS, Y ;
MERMET, JM ;
DELAPORTE, T .
ANALYTICAL CHEMISTRY, 1991, 63 (14) :1497-1498
[2]   DETERMINATION OF SILVER IN WATERS AND SOIL BY ELECTROTHERMAL ATOMIC-ABSORPTION SPECTROMETRY AFTER COMPLEXATION AND SORPTION ON CARBON [J].
AVILA, AK ;
CURTIUS, AJ .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1994, 9 (04) :543-546
[3]  
BODE H, 1962, FRESEN Z ANAL CHEM, V185, P99
[4]  
BODE H, 1962, Z ANAL CHEM, V185, P179
[5]   EVALUATION OF 3 LOW-VOLUME INTERFACES FOR ORGANIC-SOLVENT INTRODUCTION TO THE INDUCTIVELY COUPLED PLASMA - APPLICATIONS TO FLOW-INJECTION [J].
BROTHERTON, TJ ;
PFANNERSTILL, PE ;
CREED, JT ;
HEITKEMPER, DT ;
CARUSO, JA ;
PRATSINIS, SE .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1989, 4 (04) :341-345
[6]  
da Silva MAM, 2000, SPECTROCHIM ACTA B, V55, P803
[7]   Introduction of alcohols in inductively coupled plasma mass spectrometry by a flow injection system [J].
Dressler, VL ;
Pozebon, D ;
Curtius, AJ .
ANALYTICA CHIMICA ACTA, 1999, 379 (1-2) :175-183
[8]   Determination of heavy metals by inductively coupled plasma mass spectrometry after on-line separation and preconcentration [J].
Dressler, VL ;
Pozebon, D ;
Curtius, AJ .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 1998, 53 (11) :1527-1539
[9]   EFFECT OF ORGANIC-SOLVENTS AND MOLECULAR GASES ON POLYATOMIC ION INTERFERENCES IN INDUCTIVELY COUPLED PLASMA MASS-SPECTROMETRY [J].
EVANS, EH ;
EBDON, L .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1990, 5 (06) :425-429
[10]   ELIMINATION OF INTERFERENCES IN THE DETERMINATION OF ARSENIC AND SELENIUM IN BIOLOGICAL SAMPLES BY INDUCTIVELY-COUPLED PLASMA-MASS SPECTROMETRY [J].
GOOSSENS, J ;
VANHAECKE, F ;
MOENS, L ;
DAMS, R .
ANALYTICA CHIMICA ACTA, 1993, 280 (01) :137-143