Photocatalytic degradation of phenol and trichloroethylene: On-line and real-time monitoring via membrane introduction mass spectrometry

Citation
Rfp. Nogueira et al., Photocatalytic degradation of phenol and trichloroethylene: On-line and real-time monitoring via membrane introduction mass spectrometry, IND ENG RES, 38(5), 1999, pp. 1754-1758
Citations number
30
Categorie Soggetti
Chemical Engineering
Journal title
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
ISSN journal
08885885 → ACNP
Volume
38
Issue
5
Year of publication
1999
Pages
1754 - 1758
Database
ISI
SICI code
0888-5885(199905)38:5<1754:PDOPAT>2.0.ZU;2-V
Abstract
Membrane introduction mass spectrometry (MIMS) has been applied to monitor and compare in real time the extent by which three photocatalytic remediati on processes-Fenton's reagent/ UV, ferrioxalate/H2O2/UV, and TiO2/UV-destro y two common water pollutants-phenol and trichloroethylene (TCE). Continuou s MIMS and selected ion monitoring (MIMS-SIM) of both phenol and TCE degrad ation and CO2 production show first-order kinetics for the three processes. Phenol half-life times indicate that Fenton's reagent/UV and ferrioxalate/ H2O2/UV destroys phenol 10 times faster than TiO2/UV, that is, Fenton's rea gent/UV approximate to ferrioxalate/H2O2/UV >> TiO2/UV. For TCE, half-life times for the three remediation processes are ordered as follows: ferrioxal ate/H2O2/UV >> Fenton's reagent/UV > TiO2/UV. For phenol, the extent of min eralization measured via total organic carbon analysis was lower than the e xtent of degradation measured by MIMS-SIM; hence, for the three processes, the intermediate products of phenol photocatalytic degradation are slowly d estroyed. For Fenton's reagent/UV and ferrioxalate/H2O2/UV GC/MS analysis d etected pyrocatechol as the main intermediate of phenol degradation and p-b enzoquinone for TiO2/UV.