Influence of palladium content dispersed in the TiO2 photocatalyst for degradation of volatile organic compounds in gas emission.

Heterogeneous photocatalysis is highlighted to treat volatile organic compound (VOC) emission. Then, this work analysed the influence of palladium (Pd) content loaded in TiO2 on n-octane and iso-octane photodegradation. For this, TiO2 was loaded with Pd in different contents: 0.4%, 0.7%, and 1.0%. The samples were characterized, and the photodegradation experiments were conducted by Pd/TiO2/UV process. The characterization analyses showed that the metal presence did not change the catalyst structure or its surface area; however, it reduced the bandgap energy. The photocatalytic results proved that palladium improved n-octane degradation from 62% (pure TiO2) to 92.6% (0.4%Pd/TiO2) and, iso-octane degradation enhanced from 59% (pure TiO2) to 90.6% (0.7%Pd/TiO2); all results were obtained in the space time of 39 s. Therefore, 0.4%Pd/TiO2 and 0.7%Pd/TiO2 showed better oxidation results to degradation n-octane and iso-octane, respectively. The kinetic model of pseudo-first order showed a good fit for the data of both VOCs. Heterogeneous photocatalysis with Pd/TiO2 showed to be an adequate technique to reduce VOCs emission.

Catalytic oxidation at pilot-scale: Efficient degradation of volatile organic compounds in gas phase.

Volatile organic compounds (VOCs) are responsible for environmental problems and may affect human health. Several treatment technologies minimize VOCs emissions; among those, catalytic oxidation appears as a promising alternative. In this study, a pilot-scale catalytic reactor was developed and the influence of process parameters on toluene degradation were investigated. Inlet gases were heated by electrical resistances and the catalyst employed was a honeycomb shape commercial automotive catalyst (Umicore, model AFT). Toluene degradation higher than 99% was achieved for several conditions and temperature showed to be the most important process variable for it. For all concentrations, it was observed that when increasing temperature led to a decrease on the space time. At 800 ppmv, varying from 543 K to 633 K, the space time decreased from 0.121 s to 0.08 s, respectively. At 1600 ppmv for the same temperature range, space time was reduced from 0.098 s to 0.040 s, respectively. At 2400 ppmv, varying from 543 K to 633 K, space time decreased from 0.081 s to 0.048 s. The catalytic reactor developed proved to be efficient for VOCs treatment, showing a high potential of application at industrial emission sources.

Photodegradation of cyclohexane and toluene using TiO2/UV/O3 in gas phase.

Volatile organic compounds (VOC) are air pollutants usually found in urban and industrial areas. Heterogeneous photocatalysis is an interesting technique used to degrade these compounds. Several approaches may enhance this process; some studies have shown higher VOC conversions by adding ozone to the experimental system, once ozone increases the number of reactive radicals in the reaction. In this context, this work studied the conversion of cyclohexane and toluene by heterogeneous photocatalysis in gas phase, in the presence of titanium dioxide (TiO2), UV light, and different concentrations of ozone. For fixed space times from 13.1 to 48.8 s, an average increase of 9% was reached in cyclohexane conversion when comparing the system with maximum concentration of ozone (0.8%) and the system without it. In addition, difference of less than 2% in the conversion of cyclohexane with different moisture fractions was observed. Toluene photodegradation was also analyzed in the presence of ozone and although the conversion was only about 40% for the space time of 25 s, this result was maintained during 4 h of experiment, with no catalyst deactivation as usually reported in the literature for aromatic compounds. Based on the results, ozone addition is an advantageous technique to improve the photodegradation of VOC.