Mecanismo de fotodegradação de compostos orgânicos catalisada por TiO2

Conventional technology used in the treatment of wastewater has been pointed as a major environmental problem for sustainable development, since minimization is not addressed accordingly. Advanced oxidation processes (AOP), based on the formation of hydroxyl radical (•OH), a powerful oxidant agent, have been considered to be a potential technology for the destruction of many toxic compounds. Photocatalysis using solar light, an AOP, has been studied for nearly 20 years and recently attracted great interest as a clean-up technology. However, solar detoxification processes have not yet achieved commercial success. This article presents an overview of reaction mechanisms at the surface of semiconductors used as photocatalysts (specially TiO2), when heterogeneous photocatalysis is used to remove hazardous compounds from contaminated sites.

Nanoestruturas em fotocatálise: uma revisão sobre estratégias de síntese de fotocatalisadores em escala nanométrica

Advanced oxidative processes (AOPs) are based on chemical processes that can generate free radicals, such as hydroxyl radicals (.OH) which are strong, non-selective oxidant species that react with the vast majority of organic compounds. Nanostructured semiconductors, especially titanium dioxide (TiO2) in the anatase phase, are well-established photocatalysts for this process, which have proved to be useful in the degradation of dyes, pesticides and other contaminants. Research in different strategies for the synthesis of nanostructured semiconductors, with particular characteristic is currently a topic of interest in many studies. Thus, this paper presents a review about various synthesis strategies of nanostructured photocatalysts.

Degradação fotocatalítica de sulfametoxazol, trimetoprima e diclofenaco em solução aquosa

In this work the photocatalytic degradation of sulfametoxazole, trimethoprim and potassium diclofenac was evaluated by using TiO2 and ZnO photocatalysts. In optimized experimental conditions (pH 4, TiO2: 50 mg) the TiO2-photocatalysis allowed an almost total degradation of the studied drugs with mineralization of about 80% at reaction times of 120 min. Some mechanistic differences were observed between TiO2 and ZnO in the degradation study involving potassium diclofenac. At the first reaction times the use of ZnO leads to generation of transient species that strongly absorb in the UV spectral region, a fact not observed in studies involving TiO2.

ÓXIDOS DE NIÓBIO: UMA VISÃO SOBRE A SÍNTESE DO Nb2O5 E SUA APLICAÇÃO EM FOTOCATÁLISE HETEROGÊNEA

Despite the fact that Brazil is the world’s largest niobium mineral producer, governmental interest in exploration of the mineral leading to more valuable derived materials is scarce, which has reduced the country’s knowledge about a wider range of technological applications for this metal. Niobium pentoxide stands out due its remarkable electronic, structural, and textural properties. Therefore, this review aims to highlight its main properties, synthetic methods, and applications, with a particular focus on photocatalysts based on Nb2O5. This review will highlight the potential of Nb2O5 and encourage the study of niobium and its compounds in technological and environmental applications.