Detection of some industrially relevant elements in water by electrolyte cathode atmospheric glow discharge optical emission spectrometry

László Bencs, Nikoletta Laczai, P. Mezei, Tamás Cserfalvi

Research output: Contribution to journalArticle

22 Citations (Scopus)

Abstract

An electrolyte cathode atmospheric glow discharge optical emission spectrometry (ELCAD-OES) method was developed for the detection of the industrially relevant In, Rh and Te in water samples. Acid/additive type, sample pH and flow rate were optimized. The UV-Vis spectrum was scanned for analytical lines, free from spectral overlap interferences, and sensitive enough for quantifying the analytes at mg L- 1 or lower levels. In several cases, the background spectrum of the ELCAD hindered the use of conventional, resonant analytical lines in the UV due to overlaps with bands of molecular species (e.g., OH, NO, N2). Te and Rh showed lower emission intensities than In (determined at In I 451.1 nm), even using the most sensitive, interference-free transitions (i.e., Te I 214.3 nm, Te I 238.6 nm and Rh I 437.5 nm). The emission intensities were highly sample pH dependent, i.e., analytical signals could only be detected at pH levels lower than 2. Conversely, the use of acidity lower than pH 1 caused lower plasma volume, due to its contraction into the sample introduction capillary, and discharge instability in terms of its frequent self-extinction. The detection limits for In, Rh and Te were 0.01, 0.5 and 2.4 mg L- 1, respectively. Calibration curves were linear up to 100-150 mg L- 1. The precision for In, Rh and Te in aqueous standards, expressed as relative standard deviation (RSD), was not higher than 4.6%, 6.4% and 7.4%, respectively. Samples with high salt content (e.g., well water) caused positive matrix effects (i.e., 2.0- to 3.6-fold signal enhancements), but also ∼ 1.5 times higher RSDs.

Original languageEnglish
Pages (from-to)139-145
Number of pages7
JournalSpectrochimica Acta - Part B Atomic Spectroscopy
Volume107
DOIs
Publication statusPublished - May 1 2015

Fingerprint

Glow discharges
glow discharges
Spectrometry
Electrolytes
light emission
Cathodes
cathodes
electrolytes
Water
Acidity
water
spectroscopy
Salts
Flow rate
Calibration
Plasmas
Acids
interference
acidity
contraction

Keywords

  • Ambient atmospheric plasma
  • Atomic emission spectroscopy
  • Elemental content monitoring
  • Solution cathode
  • Spectral interference

ASJC Scopus subject areas

  • Instrumentation
  • Atomic and Molecular Physics, and Optics
  • Analytical Chemistry
  • Spectroscopy

Cite this

Detection of some industrially relevant elements in water by electrolyte cathode atmospheric glow discharge optical emission spectrometry. / Bencs, László; Laczai, Nikoletta; Mezei, P.; Cserfalvi, Tamás.

In: Spectrochimica Acta - Part B Atomic Spectroscopy, Vol. 107, 01.05.2015, p. 139-145.

Research output: Contribution to journalArticle

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abstract = "An electrolyte cathode atmospheric glow discharge optical emission spectrometry (ELCAD-OES) method was developed for the detection of the industrially relevant In, Rh and Te in water samples. Acid/additive type, sample pH and flow rate were optimized. The UV-Vis spectrum was scanned for analytical lines, free from spectral overlap interferences, and sensitive enough for quantifying the analytes at mg L- 1 or lower levels. In several cases, the background spectrum of the ELCAD hindered the use of conventional, resonant analytical lines in the UV due to overlaps with bands of molecular species (e.g., OH, NO, N2). Te and Rh showed lower emission intensities than In (determined at In I 451.1 nm), even using the most sensitive, interference-free transitions (i.e., Te I 214.3 nm, Te I 238.6 nm and Rh I 437.5 nm). The emission intensities were highly sample pH dependent, i.e., analytical signals could only be detected at pH levels lower than 2. Conversely, the use of acidity lower than pH 1 caused lower plasma volume, due to its contraction into the sample introduction capillary, and discharge instability in terms of its frequent self-extinction. The detection limits for In, Rh and Te were 0.01, 0.5 and 2.4 mg L- 1, respectively. Calibration curves were linear up to 100-150 mg L- 1. The precision for In, Rh and Te in aqueous standards, expressed as relative standard deviation (RSD), was not higher than 4.6{\%}, 6.4{\%} and 7.4{\%}, respectively. Samples with high salt content (e.g., well water) caused positive matrix effects (i.e., 2.0- to 3.6-fold signal enhancements), but also ∼ 1.5 times higher RSDs.",
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