scholarly journals Heterogeneous Photocatalysis and Prospects of TiO2-Based Photocatalytic DeNOxing the Atmospheric Environment

Catalysts ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 553 ◽  
Author(s):  
Nick Serpone

This article reviews the efforts of the last two decades to deNOxify the atmospheric environment with TiO2-based photocatalytic materials supported on various cementitious-like substrates. Prior to undertaking this important aspect of applied photocatalysis with metal-oxide emiconductor photocatalysts, however, it is pertinent to describe and understand the fundamentals of Heterogeneous Photocatalysis. The many attempts done in a laboratory setting to degrade (deNOxify) the major components that make up the NOx, namely nitric oxide (NO) and nitrogen dioxide (NO2), but most importantly the efforts expended in deNOxifying the real environment upon depositing titania-based coatings on various model and authentic infrastructures, such as urban roads, highway noise barriers, tunnels, and building external walls among others, are examined. Both laboratory and outdoor experimentations have been performed toward NOx being oxidized to form nitrates (NO3−) that remain adsorbed on the TiO2-based photocatalytic surfaces (except in tunnels—indoor walls) but get subsequently dislodged by rain or by periodic washings of the infrastructures. However, no serious considerations have been given to the possible conversion of NOx via photocatalytic reduction back to N2 and O2 gases that would restore the atmospheric environment, as the adsorbed nitrates block the surface-active sites of the photocatalyst and when washed-off ultimately cause unduly damages to the environment.

2013 ◽  
Vol 2013 ◽  
pp. 1-16 ◽  
Author(s):  
Huanan Cui ◽  
Hong Liu ◽  
Jianying Shi ◽  
Chuan Wang

Oxygen vacancies and Ti-related defects (OTDs) are the main lattice defects ofTiO2, which have great influence on its photocatalytic activity. To understand the relationship between the defects and photocatalytic activities, detailed discussions based on the electronic driven force provided by these defects are carried out during the three commonly accepted processes in photocatalytic reactions. It is found that these defects inevitably (i) influence the energy structure of the pristineTiO2as the isolate acceptor/donor level or hybrid with the original orbital, (ii) provide a disordered short-range force that confuses the charge carriers transferring to surface active sites, (iii) act not only as the surface active sites for trapping the charge carriers but also as the main chemisorption sites forO2,H2O, and organic species. These effects of the defects make them one of the key factors that determine the efficiency of heterogeneous photocatalysis. Clarifying the role of the defects will further facilitate the exploration and the construction of high-performance photocatalysts for practical applications.


RSC Advances ◽  
2015 ◽  
Vol 5 (104) ◽  
pp. 85319-85322 ◽  
Author(s):  
V. Nahuel Montesinos ◽  
Natalia Quici ◽  
Hugo Destaillats ◽  
Marta I. Litter

For the first time, nitric oxide (NO), a precursor of nitrogen dioxide (a NIOSH-listed pollutant), has been found to be one of the final products of the photocatalytic reduction of nitrate in water using TiO2 and formic acid as a hole scavenger.


1993 ◽  
Vol 58 (7) ◽  
pp. 1591-1599 ◽  
Author(s):  
Abd El-Aziz A. Said

Molybdenum oxide catalyst doped or mixed with (1 - 50) mole % Fe3+ ions were prepared. The structure of the original samples and the samples calcined at 400 °C were characterized using DTA, X-ray diffraction and IR spectra. Measurements of the electrical conductivity of calcined samples with and without isopropyl alcohol revealed that the conductance increases on increasing the content of Fe3+ ions up to 50 mole %. The activation energies of charge carriers were determined in presence and absence of the alcohol. The catalytic dehydration of isopropyl alcohol was carried out at 250 °C using a flow system. The results obtained showed that the doped or mixed catalysts are active and selective towards propene formation. However, the catalyst containing 40 mole % Fe3+ ions exhibited the highest activity and selectivity. Correlations were attempted to the catalyst composition with their electronic and catalytic properties. Probable mechanism for the dehydration process is proposed in terms of surface active sites.


Sign in / Sign up

Export Citation Format

Share Document