Preparation characterization and photocatalytic activity of polycrystalline ZnO/TiO2 systems. 2. Surface, bulk characterization, and 4-nitrophenol photodegradation in liquid-solid regime
G. Marci et al., Preparation characterization and photocatalytic activity of polycrystalline ZnO/TiO2 systems. 2. Surface, bulk characterization, and 4-nitrophenol photodegradation in liquid-solid regime, J PHYS CH B, 105(5), 2001, pp. 1033-1040
Electron spin resonance spectroscopy (ESR), Fourier transform infrared spec
troscopy (FTIR), and monitoring of pyridine (py) and boric acid trimethyl e
ster (BATE) adsorption for determining surface acidity and basicity, respec
tively, were used to carry out further characterization of mixed ZnO/TiO2 p
olycrystalline solids prepared by different methods. Moreover, the powders
were tested in a batch photoreactor for a probe reaction, i.e., 4-nitrophen
ol photodegradation in aqueous medium. ESR results indicated the presence o
f signals attributable to Zn+ species in ZnO/TiO2 (anatase) solids, while i
n ZnO/TiO2 (rutile) samples the presence of zinc induced only the formation
of signals probably due to Ti3+ centers. FT-IR spectra showed no significa
nt differences of the surface hydroxylation degree of the various photocata
lysts, whereas the surface acidic properties generally decrease by increasi
ng the amount of ZnO, Coupling of ZnO and TiO2 semiconducting powders was n
ot so beneficial, as expected on the basis of the intrinsic electronic prop
erties, to enhance the photoreactivity for the studied reaction, although s
ome of the powders showed photoactivities slightly higher than those of bar
e TiO2 and ZnO. Nevertheless, some of the samples (the mixed particles ZnO/
TiO2 (rutile)) appear promising from an application point of view because n
o filtration tvas needed after the occurrence of the photoreactivity tests
to separate them from the solution because they decanted easily. The minera
lization of 4-nitrophenol was checked by determining the total organic carb
on (TOC) and a complete photooxidation occurred in few hours in the presenc
e of some of the samples.