Research Journal of Pharmacy and Technology
Year : 2019, Volume : 12, Issue : 6
First page : ( 2828) Last page : ( 2831)
Print ISSN : 0974-3618. Online ISSN : 0974-360X.
Article DOI : 10.5958/0974-360X.2019.00476.1

Montmorillonite Nanoclay Interaction with 2-Aminophenol and 2-Nitrophenol

Hassen Jasim Hamadi*

Assistant Professor, College of Pharmacy, University of Anbar, Ramadi, Iraq

*Corresponding Author E-mail: Jasimhu@hotmail.com

Online published on 8 August, 2019.

Abstract

The interaction of 2-aminophenol and 2-nitrophenol compounds with the structural iron of montmorillonite nanoclay was studied using Mössbauer spectroscopy in order to determine what effects have the groups of withdrawing and donating electrons on the phenol ring and how they affect the nanoclay structural iron. 100 mg of the organic compound was dissolved in 50 ml distilled water in 100 ml volumetric flask. 1 gm of the montmorillonite nanoclay was added to this solution. The mixture was stirred for 24 hours in order to reach equilibrium, then filtered. It was found that the structural iron (III) of the montmorillonite nanoclay sample can be reduced to iron (II). The reduction process depends on the substituent on the phenolic ring. At high pH, reduction takes place if the phenolic ring has electron donating substituent like NH2, while no reduction occurs if the phenolic ring has electron withdrawing substituent like NO2. The process involves electron transfer from the hydroxyl group on the compound substituted with donating group, to the active site at the iron atoms within the montmorillonite lattice. This site is considered to be Lewis acid.

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Keywords

Mössbauer spectroscopy, nanoclay, montmorillonite, phenolic ring, donating substituent, withdrawing substituent.

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