Acquiring Information on the Total Content and Speciation of Silicon in Petroleum Products/Fuels Using High-Resolution Continuum Source Flame Atomic Absorption Spectrometry and Wavelength-Dispersive X-ray Fluorescence

Zofia Kowalewska , Karolina Brzezińska , Katarzyna Cikorska , Janusz Pilarczyk , Łukasz Gościniak

Abstract

Various chemical forms of silicon (Si) possibly present in petroleum products/fuels were investigated in this work: low-molecular-mass species with different compositions, structures, and volatilities, as well as a Conostan oil standard, polysiloxanes, and silicon dioxide. Analysis in xylene solutions was accomplished using wavelength-dispersive X-ray fluorescence (WD XRF) or high-resolution continuum source flame atomic absorption spectrometry (HR-CS FAAS). Samples were also analyzed using HR-CS FAAS in aqueous solutions after mineralization in a closed microwave-heated system, mineralization in an open system, or mineralization combined with fusion using lithium metaborate. It was found that none of the applied procedures was suitable for the accurate determination of Si in all the tested forms. The total content of Si can only be determined if various methodological variants are applied. Using WD XRF, similar signals are obtained for all the investigated organic Si forms. The procedure is also helpful to detect sedimentation (presence) of inorganic Si compounds (successive measurements in the same cup). In direct measurements of organic solutions using HR-CS FAAS, analytical response is similar for all the investigated organic forms, apart from the significantly increased signal for the most volatile forms. On the other hand, underestimated results due to losses of volatile and moderately volatile Si compounds and/or difficulty in analyte transfer to an aqueous solution in the mineralization procedures were stated. The procedure combining mineralization and fusion gave quantitative results for SiO2, the Conostan standard, and some polysiloxanes. The similar behavior of Si compounds belonging to a given group (organic very volatile, moderately volatile, nonvolatile, or inorganic), leading to a systematic error in a given procedure, was used to acquire knowledge on the presence of the kind of Si species in a sample. The proposed analytical scheme employs easy available analytical techniques and can be widely applied. It was also found that internal standard calibration available in HR-CS FAAS does not correct chemical interference due to the LiBO2 matrix. However, using vanadium (V) as the internal standard, it is possible to correct sensitivity drift with time.
Author Zofia Kowalewska (FCEMP / IC)
Zofia Kowalewska,,
- The Institute of Chemistry
, Karolina Brzezińska (FCEMP / IC)
Karolina Brzezińska,,
- The Institute of Chemistry
, Katarzyna Cikorska
Katarzyna Cikorska,,
-
, Janusz Pilarczyk
Janusz Pilarczyk,,
-
, Łukasz Gościniak (FCEMP / IC)
Łukasz Gościniak,,
- The Institute of Chemistry
Journal seriesEnergy & Fuels, ISSN 0887-0624, (A 35 pkt)
Issue year2019
Vol33
No1
Pages215-227
Publication size in sheets0.6
Keywords in PolishOznaczanie krzemu; specjacja krzemu; analiza specjacyjna; HR-CS; HR-CS AAS; WD XRF; wzorzec wewnętrzny; mineralizacja; stapianie; ditlenek krzemu; wzorzec Conostan; efekt formy analitu
Keywords in EnglishSilicon determination; silicon speciation; speciation analysis; HR-CS; HR-CS AAS; WD XRF; internal standard; mineralization; fusion; silicon dioxide; Conostan standard; analyte form effect
ASJC Classification2102 Energy Engineering and Power Technology; 2103 Fuel Technology; 1500 General Chemical Engineering
DOIDOI:10.1021/acs.energyfuels.8b03517
Languageen angielski
Score (nominal)35
ScoreMinisterial score = 35.0, 23-05-2019, ArticleFromJournal
Publication indicators WoS Citations = 0; Scopus SNIP (Source Normalised Impact per Paper): 2017 = 1.276; WoS Impact Factor: 2017 = 3.024 (2) - 2017=3.622 (5)
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