Photocatalytic oxidation of fuel oxygenated additives in aqueous solutions

Experimental research of photocatalytical oxidation (PCO) of aqueous solutions of de-icing agents (ethylene glycol and ethylene glycol monoethyl ether) and methyl tert-butyl ether (MTBE) was undertaken. These chemicals are water-soluble components of jet and motor fuels accidentally disposed to the...

Full description

Saved in:
Bibliographic Details
Main Authors: M. Krichevskaya, A. Kachina, T. Malygina, S. Preis, J. Kallas
Format: Article
Language:English
Published: Wiley 2003-01-01
Series:International Journal of Photoenergy
Online Access:http://dx.doi.org/10.1155/S1110662X03000175
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832559122105499648
author M. Krichevskaya
A. Kachina
T. Malygina
S. Preis
J. Kallas
author_facet M. Krichevskaya
A. Kachina
T. Malygina
S. Preis
J. Kallas
author_sort M. Krichevskaya
collection DOAJ
description Experimental research of photocatalytical oxidation (PCO) of aqueous solutions of de-icing agents (ethylene glycol and ethylene glycol monoethyl ether) and methyl tert-butyl ether (MTBE) was undertaken. These chemicals are water-soluble components of jet and motor fuels accidentally disposed to the environment. Titanium dioxide (Degussa P25) under near-UV irradiation was selected as a photocatalyst. A slightly acidic medium was preferable for the process efficiency for MTBE, whereas a neutral medium was beneficial for de-icing agents and jet fuel aqueous extracts. TiO2 suspension fractional composition was found to be dependent on pH and the presence of organic admixtures: the minimum size of TiO2 particles at their maximum uniformity was established in an acidic medium, where the efficiency of PCO of de-icing agents was the poorest. On the other hand, neutral and slightly acidic media, beneficial for PCO efficiency, were favourable for particle agglomeration, which indicates a minimal role for photocatalyst particle size in PCO efficiency. PCO efficiency increased with increasing MTBE and icing inhibitor concentration. The biodegradability of aqueous solutions of oxygenated additives increased as PCO proceeded. The influence of mineral additives—sulphate, calcium, ferric and manganese ions—on the process efficiency was found to be complex. Special attention was paid to energy-saving PCO with a photocatalyst attached to buoyant glass micro-spheres and reduced intensity of stirring of the slurry.
format Article
id doaj-art-166484a00b694e338c05452134256550
institution Kabale University
issn 1110-662X
language English
publishDate 2003-01-01
publisher Wiley
record_format Article
series International Journal of Photoenergy
spelling doaj-art-166484a00b694e338c054521342565502025-02-03T01:30:48ZengWileyInternational Journal of Photoenergy1110-662X2003-01-0152818610.1155/S1110662X03000175Photocatalytic oxidation of fuel oxygenated additives in aqueous solutionsM. Krichevskaya0A. Kachina1T. Malygina2S. Preis3J. Kallas4Institute of Chemistry at Tallinn Technical University, 15 Akadeemia tee, Tallinn 12618, EstoniaTallinn Technical University, 5 Ehitajate tee, Tallinn 19086, EstoniaTallinn Technical University, 5 Ehitajate tee, Tallinn 19086, EstoniaLappeenranta University of Technology, P. O. Box 20, Lappeenranta 53851, FinlandLappeenranta University of Technology, P. O. Box 20, Lappeenranta 53851, FinlandExperimental research of photocatalytical oxidation (PCO) of aqueous solutions of de-icing agents (ethylene glycol and ethylene glycol monoethyl ether) and methyl tert-butyl ether (MTBE) was undertaken. These chemicals are water-soluble components of jet and motor fuels accidentally disposed to the environment. Titanium dioxide (Degussa P25) under near-UV irradiation was selected as a photocatalyst. A slightly acidic medium was preferable for the process efficiency for MTBE, whereas a neutral medium was beneficial for de-icing agents and jet fuel aqueous extracts. TiO2 suspension fractional composition was found to be dependent on pH and the presence of organic admixtures: the minimum size of TiO2 particles at their maximum uniformity was established in an acidic medium, where the efficiency of PCO of de-icing agents was the poorest. On the other hand, neutral and slightly acidic media, beneficial for PCO efficiency, were favourable for particle agglomeration, which indicates a minimal role for photocatalyst particle size in PCO efficiency. PCO efficiency increased with increasing MTBE and icing inhibitor concentration. The biodegradability of aqueous solutions of oxygenated additives increased as PCO proceeded. The influence of mineral additives—sulphate, calcium, ferric and manganese ions—on the process efficiency was found to be complex. Special attention was paid to energy-saving PCO with a photocatalyst attached to buoyant glass micro-spheres and reduced intensity of stirring of the slurry.http://dx.doi.org/10.1155/S1110662X03000175
spellingShingle M. Krichevskaya
A. Kachina
T. Malygina
S. Preis
J. Kallas
Photocatalytic oxidation of fuel oxygenated additives in aqueous solutions
International Journal of Photoenergy
title Photocatalytic oxidation of fuel oxygenated additives in aqueous solutions
title_full Photocatalytic oxidation of fuel oxygenated additives in aqueous solutions
title_fullStr Photocatalytic oxidation of fuel oxygenated additives in aqueous solutions
title_full_unstemmed Photocatalytic oxidation of fuel oxygenated additives in aqueous solutions
title_short Photocatalytic oxidation of fuel oxygenated additives in aqueous solutions
title_sort photocatalytic oxidation of fuel oxygenated additives in aqueous solutions
url http://dx.doi.org/10.1155/S1110662X03000175
work_keys_str_mv AT mkrichevskaya photocatalyticoxidationoffueloxygenatedadditivesinaqueoussolutions
AT akachina photocatalyticoxidationoffueloxygenatedadditivesinaqueoussolutions
AT tmalygina photocatalyticoxidationoffueloxygenatedadditivesinaqueoussolutions
AT spreis photocatalyticoxidationoffueloxygenatedadditivesinaqueoussolutions
AT jkallas photocatalyticoxidationoffueloxygenatedadditivesinaqueoussolutions