Molybdenum (VI) binded to humic and nitrohumic acid models in aqueous solutions. Salicylic, 3-nitrosalicylic, 5-nitrosalicylic and 3,5 dinitrosalicylic acids: part 2

• Main Authors: Mercê Ana Lucia R., Lopes Priscilla P., Mangrich Antonio S., Levy Noel M.
• Format: Article
• Language: English
• Published: Sociedade Brasileira de Química 2006-01-01
• Series: Journal of the Brazilian Chemical Society
• Subjects: humic acid models; molybdenum (VI); potentiometric titration; stability constants; slow release fertilizer; electrochemistry; complexation; UV-Vis
• Online Access: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532006000300008
• ISSN: 0103-5053; 1678-4790

In this work electrochemical and Ultraviolet-Visible studies were performed in solutions of salicylic acid models of humic and nitrohumic acids, a laboratory artifact, and molybdenum in order to determine the affinity of these models towards the metal ion. Molybdenum, which plays a very important role in the soil chemistry, and together with humic substances, impart fertility to soil and water and is a key element in the activity of nitrogenase. The obtained results showed that at least one complexed species is present at the pH range of 6.3 to 8.0, even for the less basic chosen models, the nitrosalicylic acids. Previous study showed that phthalic and nitrophthalic, also humic and nitrohumic acids model compounds, presented complexed species with molybdenum only till pH 6.5. The calculated formation constants showed that the substitution of the nitro group in the orto position was less favoured than in the para substitution, probably due to a steric hindrance in the former, which was clearly seen in the double substituted salicylic nitro derivative. The cyclic voltammetry as well as the Ultraviolet-Visible obtained spectra were able to show that the chemistry of molybdenum in aqueous solutions as the pH is increased is very complex, and the molybdate stops acting as an anion only after pH around 4, when it finally becomes a cation MoO2(2+) (M).