Generation of Free OHaq Radicals by Black Light Illumination of Degussa (Evonik) P25 TiO2 Aqueous Suspensions
This work demonstrates how formation of strongly chemiluminescent 3-hydroxyphthalic hydrazide by hydroxylation of non-chemiluminescent phthalic hydrazide can be applied as a selective reaction probe to obtain information on authentic hydroxyl radical, i.e., •OHaq, formation, in black light illuminat...
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doaj-5886270b399c4927afa37f02d22e381a2020-11-24T21:11:08ZengMDPI AGCatalysts2073-43442013-04-013241844310.3390/catal3020418Generation of Free OHaq Radicals by Black Light Illumination of Degussa (Evonik) P25 TiO2 Aqueous SuspensionsTorbjörn ReitbergerHaidong LiaoThis work demonstrates how formation of strongly chemiluminescent 3-hydroxyphthalic hydrazide by hydroxylation of non-chemiluminescent phthalic hydrazide can be applied as a selective reaction probe to obtain information on authentic hydroxyl radical, i.e., •OHaq, formation, in black light illuminated Degussa P25 TiO2 aerated suspensions in the pH range from 3 to 11. The •OHaq formation was found to be strongly pH dependent. At alkaline pH, the apparent quantum efficiency of •OHaq formation was estimated to be at the ~10−2 level whereas at acidic pH it was near zero. Addition of phosphate and fluoride ions substantially enhanced the •OHaq production in the acidic pH range. It is suggested that •OHaq-radical formation in TiO2 photocatalysis can occur by oxidation of hydroxyl ions in the water layer adsorbed on TiO2 surfaces.http://www.mdpi.com/2073-4344/3/2/418photocatalysisTiO2•OHaq radicalchemiluminescence |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Torbjörn Reitberger Haidong Liao |
spellingShingle |
Torbjörn Reitberger Haidong Liao Generation of Free OHaq Radicals by Black Light Illumination of Degussa (Evonik) P25 TiO2 Aqueous Suspensions Catalysts photocatalysis TiO2 •OHaq radical chemiluminescence |
author_facet |
Torbjörn Reitberger Haidong Liao |
author_sort |
Torbjörn Reitberger |
title |
Generation of Free OHaq Radicals by Black Light Illumination of Degussa (Evonik) P25 TiO2 Aqueous Suspensions |
title_short |
Generation of Free OHaq Radicals by Black Light Illumination of Degussa (Evonik) P25 TiO2 Aqueous Suspensions |
title_full |
Generation of Free OHaq Radicals by Black Light Illumination of Degussa (Evonik) P25 TiO2 Aqueous Suspensions |
title_fullStr |
Generation of Free OHaq Radicals by Black Light Illumination of Degussa (Evonik) P25 TiO2 Aqueous Suspensions |
title_full_unstemmed |
Generation of Free OHaq Radicals by Black Light Illumination of Degussa (Evonik) P25 TiO2 Aqueous Suspensions |
title_sort |
generation of free ohaq radicals by black light illumination of degussa (evonik) p25 tio2 aqueous suspensions |
publisher |
MDPI AG |
series |
Catalysts |
issn |
2073-4344 |
publishDate |
2013-04-01 |
description |
This work demonstrates how formation of strongly chemiluminescent 3-hydroxyphthalic hydrazide by hydroxylation of non-chemiluminescent phthalic hydrazide can be applied as a selective reaction probe to obtain information on authentic hydroxyl radical, i.e., •OHaq, formation, in black light illuminated Degussa P25 TiO2 aerated suspensions in the pH range from 3 to 11. The •OHaq formation was found to be strongly pH dependent. At alkaline pH, the apparent quantum efficiency of •OHaq formation was estimated to be at the ~10−2 level whereas at acidic pH it was near zero. Addition of phosphate and fluoride ions substantially enhanced the •OHaq production in the acidic pH range. It is suggested that •OHaq-radical formation in TiO2 photocatalysis can occur by oxidation of hydroxyl ions in the water layer adsorbed on TiO2 surfaces. |
topic |
photocatalysis TiO2 •OHaq radical chemiluminescence |
url |
http://www.mdpi.com/2073-4344/3/2/418 |
work_keys_str_mv |
AT torbjornreitberger generationoffreeohaqradicalsbyblacklightilluminationofdegussaevonikp25tio2aqueoussuspensions AT haidongliao generationoffreeohaqradicalsbyblacklightilluminationofdegussaevonikp25tio2aqueoussuspensions |
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1716754388047888384 |