1998
DOI: 10.1016/s0003-2670(98)00546-7
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Gas chromatography–atomic emission detection for quantification of polycyclic aromatic sulfur heterocycles

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Cited by 18 publications
(13 citation statements)
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“…These spectroscopic interferences can be avoided by desolvation, the introduction of a reaction-collision cell or a combination of both [26][27][28][29][30] as well by as the use of high resolution ICP-MS [31]. On the other hand, inductively coupled plasma-atomic emission spectroscopy (ICP-AES) has also been used for the determination of elementary sulfur [32,33]. Nakahara et al described a method based on helium microwave-induced plasma (MIP-AES), where the sample was introduced in gas-phase, for the determination of sulfide and sulfite in aqueous samples [34].…”
Section: Introductionmentioning
confidence: 99%
“…These spectroscopic interferences can be avoided by desolvation, the introduction of a reaction-collision cell or a combination of both [26][27][28][29][30] as well by as the use of high resolution ICP-MS [31]. On the other hand, inductively coupled plasma-atomic emission spectroscopy (ICP-AES) has also been used for the determination of elementary sulfur [32,33]. Nakahara et al described a method based on helium microwave-induced plasma (MIP-AES), where the sample was introduced in gas-phase, for the determination of sulfide and sulfite in aqueous samples [34].…”
Section: Introductionmentioning
confidence: 99%
“…This has been contradicted by other findings that report an identical response for sulfur in different functional groups [52,56,57] and in 15 compounds containing the same functional group but of different molecular weight, for which the average deviation of the response factor from the real value was 4.0% (for 0.1 ng sulfur injected) [58]. Overloading of the detector leads to a lower response [58]. It has been postulated that tailing of the sulfur peaks as a result of interactions with the plasma quartz tube were responsible for difficulties in integrating the peak areas which led to large variation in the dependence of relative response factors on concentration; no dependence on the identity of the compounds could be demonstrated [53].…”
Section: Compound-independent Calibration For Chlorinementioning
confidence: 66%
“…The closer the chemical structure of the reference compound was to that of the analyte, the better the quantification. This has been contradicted by other findings that report an identical response for sulfur in different functional groups [52,56,57] and in 15 compounds containing the same functional group but of different molecular weight, for which the average deviation of the response factor from the real value was 4.0% (for 0.1 ng sulfur injected) [58]. Overloading of the detector leads to a lower response [58].…”
Section: Compound-independent Calibration For Chlorinementioning
confidence: 83%
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“…(4)) GC-MIP-AED --- [90] obtained by using different detectors such as ECD, ICP-MS, MIP-AED (microwave induced plasma with atomic elemental detector), and ESI-MS (electrospray mass spectrometry) observing that the best results were obtained with the ECD detector. In an other attempts to analyze halogenated VOCs in seawater samples, GC-MIP-OES was used to separate and determine chlorinated VOCs [45].…”
Section: Determination Of Chlorine-containing Speciesmentioning
confidence: 99%