Synthesis characterization and analytical applications of new chelating resin of formaldehyde-condensed phenolic schiff base

A new chelating phenolic Schiff base containing phthalate imide pendant group resin was synthesized by three steps. The first step includes synthesis of 2-(4-aminobiphenyl-4- ylcarbamoyl) benzoic acid (1), Via reaction of pthalic anhydride with benzidine. In the second lines, the compound that we ob...

Full description

Saved in:
Bibliographic Details
Published in:Ibn Al-Haitham Journal for Pure and Applied Sciences Vol. 31; no. 2; pp. 97 - 114
Main Authors: Umran, Khalidah Abbas, Laftah, Shayma Umran
Format: Journal Article
Language:English
Published: Baghdad, Iraq University of Baghdad, College of Education for Pure Science / Ibn al-Haitham 12-09-2018
University of Baghdad
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:A new chelating phenolic Schiff base containing phthalate imide pendant group resin was synthesized by three steps. The first step includes synthesis of 2-(4-aminobiphenyl-4- ylcarbamoyl) benzoic acid (1), Via reaction of pthalic anhydride with benzidine. In the second lines, the compound that we obtained in the first step was reacted with ohydroxybenzaldehyde to obtain phenolic Schiff base 2-(4'-(2-hydroxybenzylideneamino) bephenyl-4-yl carbamoyl) benzoic acid (2) The third step includes prepared resin during intensification Schiff base derived with formaldehyde inan alkaline middle. Thepthale amice acid, Schiff base and resin were characterized by various instrumental techniques like FT-IR, CNMR and elemental analysis, thermal behavior of the polymer was investigated 13 HNMR , 1 by DSC and TGA.SEM analysis of polymer shows the amorphous structure of polymer. The chelating behaviors was examined against Ni (ᴨ), Cd (ᴨ), Cr(ш)and Pb(ᴨ). using patch method in different conditions like treatment time and pH at room temperature. The resin shows a good loading capacity.
ISSN:1609-4042
2521-3407
DOI:10.30526/31.2.1961