Decatungstate anion as an efficient photocatalytic species for the transformation of the pesticide 2-(1-naphthyl)acetamide in aqueous solution

• Type: Article in International Scientific Journal
• Date: 2017

Authors

Da Silva, ES (Author) FEUP; Sarakha, M (Author) Other; Burrows, HD (Author) Other; Wong Wah Chung, P (Author) Other

Journal

Title: Journal of Photochemistry and Photobiology A: Chemistry

Vol. 334

Pages: 61-73

ISSN: 1010-6030

Publisher: Elsevier

Indexing

ISI Web of Knowledge - 4 Citations

Scopus - 4 Citations

Other information

Authenticus ID: P-00M-BK9

DOI: 10.1016/j.jphotochem.2016.10.036

Abstract (EN): The degradation and mineralization of the plant, growth regulator 2-(1-naphthyl)acetamide (NAD) was studied by excitation in the presence of the catalyst polyoxometalate decatungstate anion (W-O-10(32)4-) in aqueous solution under UV (365 nm) or simulated solar light exposure. Our results indicate that the photocatalytic degradation of NAD is dependent on molecular oxygen concentration: in aerated conditions, 95% degradation was achieved after 22 h irradiation, and followed first-order kinetics with a rate constant of 3.2 x 10(-3) min(-1), while under de-aerated conditions almost no degradation was observed (6.0% after 22 h). Upon UV irradiation, the catalyst W10O324- enhanced NAD photodegradation by a factor of about 20 compared to its direct degradation. Oxygen appeared to play a key role on the regeneration of the catalyst, promoting the photocatalytic cycle. The primary photoproducts of NAD photocatalytic degradation were assessed by LC-ESI-MS/MS, from which a mechanism of degradation involving electron transfer and hydrogen atom abstraction is proposed. Under these conditions, mono and di-hydroxylated and oxidized products similar to those obtained under direct photolysis have been identified. In addition, tri-hydroxylation and hydroxyl-naphthoquinone products have been identified exclusively when photolysis was carried out in presence of this catalyst. For prolonged photolysis times, it is expected that the irradiation of the tri-hydroxylated products leads to the opening of the aromatic ring and to mineralization. Furthermore, mineralization was achieved, and led to the formation of the inorganic ions NO2- (<6.0 mu g L-1), NO3- (2.6 mg L-1) and NH4+ (<0.5 mu g L-1).

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 13