Effect of polar and movable (OH or NH2 groups) on the photocatalytic H2 production of alkyl-alkanolamine

A comparative study

verfasst von
A.F. Alkaim, R. Dillert, D.W. Bahnemann
Abstract

The photocatalytic production of molecular hydrogen (H

2) from aqueous solutions of alkyl-alkanolamines (triethanolamine (tri-EOA), diethanolamine (di-EOA), ethanolamine (EOA), ethylamine (EA) and ethanol over Pt-loaded commercial (Sachtleben Hombikat UV100) nanoparticle titanium dioxide photocatalysts was studied. These photocatalysts were characterized using X-ray diffraction, Brunauer-Emmett-Teller, field-emission scanning electron microscopy, atomic force microscopy and UV-vis diffuse reflectance spectroscopy techniques. Effect of pH and temperature on photocatalytic hydrogen production of alkyl-alkanolamines was investigated. It was found for all molecules under study that the amount of hydrogen produced at a constant illumination time is a function of pH and temperature. At all temperatures investigated the rate of hydrogen production at pH 9 followed the order tri-EOAethanolamine >> di-EOA ≈ EOA > ethanol > EA. From the values of the photocatalytic rate constants at various temperatures, the apparent activation energies were determined for the hydrogen production. The observed dependence ofthe reaction rate on solution temperature cannot be related to light-driven reaction steps, because the band-gap energy of the semiconductor is too high for thermal excitation to become significant in the temperature range investigated.

Organisationseinheit(en)
Institut für Technische Chemie
Typ
Artikel
Journal
Environmental Technology (United Kingdom)
Band
36
Seiten
2190-2197
Anzahl der Seiten
8
ISSN
0959-3330
Publikationsdatum
02.09.2015
Publikationsstatus
Veröffentlicht
Peer-reviewed
Ja
ASJC Scopus Sachgebiete
Umweltchemie, Gewässerkunde und -technologie, Abfallwirtschaft und -entsorgung
Ziele für nachhaltige Entwicklung
SDG 7 – Erschwingliche und saubere Energie
Elektronische Version(en)
https://doi.org/10.1080/09593330.2015.1024757 (Zugang: Geschlossen)