Determination of trace elements in refined gold samples by inductively coupled plasma atomic emission spectrometry

被引:4
作者
Steharnik, Mirjana [1 ]
Todorovic, Marija [2 ]
Manojlovic, Dragan [2 ]
Stankovic, Dalibor [2 ]
Mutic, Jelena [2 ]
Trujic, Vlastimir [1 ]
机构
[1] Min & Met Inst Bor, Dept Chem Invest, Bor 19210, Serbia
[2] Univ Belgrade, Fac Chem, Belgrade 11000, Serbia
关键词
refined gold samples; trace elements; ICP-AES; certified reference material of high purity gold AuGHP1; HIGH-PURITY GOLD; OPERATING-CONDITIONS; MASS SPECTROMETRY; ABSORPTION-SPECTROMETRY; INTERNAL STANDARDIZATION; MATRIX SEPARATION; AAS DETERMINATION; FINE GOLD; PURE GOLD; METALS;
D O I
10.2298/JSC120505135S
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This paper presents a method for the determination of trace contents of silver, copper, iron, palladium, zinc and platinum in refined gold samples. A simultaneous inductively coupled plasma atomic emission spectrometer in the radial torch position and with a cross flow nebulizer was used for the determinations. In order to compare the different calibration strategies, two sets of calibration standards were prepared. The first set was based on matrix matched calibration standards and the second was prepared without the addition of matrix material. The detection limits for the matrix-matched calibrations were higher for some elements than those without matrix matching. In addition, the internal standardization method was applied and experiments indicated that indium was the best option as the internal standard. The obtained results for gold samples with matrix matched and matrix free calibrations were compared with the results obtained by the standard addition method. The accuracy of the methods was tested by performing a recovery test. The recoveries for the spiked sample were in the range of 90-115 %. The accuracy of the methods was also tested by analysis of a certified reference material of high purity gold AuGHP1. The best results were achieved by matrix free calibration and standard addition method using indium as the internal standard at a wavelength of 230 nm.
引用
收藏
页码:565 / 577
页数:13
相关论文
共 44 条
[1]   DETERMINATION OF TRACE AMOUNTS OF PALLADIUM, IRON AND COPPER IN PURE GOLD BY INDUCTIVELY COUPLED PLASMA ATOMIC EMISSION-SPECTROMETRY [J].
BAUCELLS, M ;
LACORT, G ;
ROURA, M .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1987, 2 (06) :645-647
[2]   Determination of arsenic in gold by flow injection inductively coupled plasma mass spectrometry with matrix removal by reductive precipitation [J].
BecotteHaigh, P ;
Tyson, JF ;
Denoyer, E ;
Hinds, MW .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 1996, 51 (14) :1823-1827
[3]   Determination of arsenic in gold samples using matrix exchange differential pulse stripping voltammetry [J].
Billling, C ;
Groot, DR ;
van Staden, JF .
ANALYTICA CHIMICA ACTA, 2002, 453 (02) :201-208
[4]  
Calliari I, 2000, X-RAY SPECTROM, V29, P438, DOI 10.1002/1097-4539(200011/12)29:6<438::AID-XRS450>3.0.CO
[5]  
2-0
[6]   DRIFT DIAGNOSTICS IN INDUCTIVELY COUPLED PLASMA ATOMIC EMISSION-SPECTROMETRY [J].
CARRE, M ;
POUSSEL, E ;
MERMET, JM .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1992, 7 (06) :791-797
[7]  
Dan S. D., 2001, SPECTROSC SPECT ANAL, V21, P849
[8]   Comparison of the effect of acetic acid with axially and radially viewed inductively coupled plasma atomic emission spectrometry: influence of the operating conditions [J].
Dubuisson, C ;
Poussel, E ;
Mermet, JM ;
Todoli, JL .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1998, 13 (01) :63-67
[9]   Comparison of ionic line-based internal standardization with axially and radially viewed inductively coupled plasma atomic emission spectrometry to compensate for sodium effects on accuracy [J].
Dubuisson, C ;
Poussel, E ;
Mermet, JM .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1998, 13 (11) :1265-1269
[10]   Effect of sodium during the aerosol transport and filtering in inductively coupled plasma atomic emission spectrometry [J].
Dubuisson, C ;
Poussel, E ;
Todoli, JL ;
Mermet, JM .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 1998, 53 (04) :593-600