2 research outputs found
Solar Light Degradation of Trimethyl Phosphate and Triethyl Phosphate on Dry and Water-Precovered Hematite and Goethite Nanoparticles
We report on the solar-light-mediated degradation of
trimethyl
phosphate (TMP) and triethyl phosphate (TEP) on hematite and goethite
nanoparticles in synthetic air. Adsorption and photoreactions of TMP
and TEP were studied by in situ diffuse reflectance Fourier transform
infrared spectroscopy (DRIFTS) on dry and water-precovered
nanoparticles in dark and under simulated solar light irradiation.
Two-dimensional correlation analysis of infrared spectra was used
to identify surface products as a function of reaction time. The optical
properties of the hematite and goethite nanoparticles were investigated
with optical spectrophotometry. The optical band gap was determined
by analysis of the Tauc relationship around the band gap energy, <i>E</i><sub>g</sub>, yielding band gap energies of 2.14 and 2.28
eV for hematite and goethite nanoparticles, respectively. It is found
that both TMP and TEP are readily photodegraded upon solar light irradiation
(employing AM1.5 filters with 1735 W m<sup>ā2</sup>), yielding
surface orthophosphate as the final product. The first step in the
dissociation of TMP and TEP is displacement of the methoxy and ethoxy
groups, respectively, yielding adsorbed dimethyl phosphate (DMP) and
methoxy, and diethyl phosphate (DEP) and ethoxy intermediates. Further
photodegradation displaces additional methoxy and ethoxy groups with
adsorbed orthophosphate as final reaction product. Methoxy and ethoxy
fragments are simultaneously oxidized to carboxylates and carbonates.
Photodegradation of TMP and TEP is promoted by OH radicals, which
is evidenced by the higher photodegradation rate on water-precovered
surfaces. The rate of TMP degradation is higher than that for TEP,
contrary to what is expected from their corresponding bulk hydrolysis
rates, but consistent with their surface reactivity in dark, where
TMP is observed to dissociate at room temperature but not TEP (or
only very slowly). The photodegradation rate is higher on the goethite
nanoparticles than the hematite nanoparticles on both dry and water
precovered surfaces. The TMP and TEP photodegradation rate constants
are found to be 0.025 (0.058) and 0.008 (0.023) min<sup>ā1</sup>, respectively, on water-precovered hematite (goethite) nanoparticles