## Abstract The synthesis, characterization, and metal ion uptake studies of two chelating resins with multiple functional groups are reported. The chelating resins were synthesized by condensing a phenolic Schiff base derived from 4,4′‐diaminodiphenylmethane and __o__‐hydroxyacetophenone with form
Chelating resins VII: studies on chelating resins of formaldehyde and furfuraldehyde-condensed phenolic Schiff base derived from 4,4′-diaminodiphenylsulphone and o-hydroxyacetophenone
✍ Scribed by S Samal; N.K Mohapatra; S Acharya; R.K Dey
- Book ID
- 104425691
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 472 KB
- Volume
- 42
- Category
- Article
- ISSN
- 1381-5148
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✦ Synopsis
The synthesis, characterization and capacity studies of two chelating resins having multiple functional groups capable of coordinating to several metal ions are reported. The resins were synthesized by condensing phenolic Schiff bases derived from 4,49-diaminodiphenylsulphone and o-hydroxyacetophenone with formaldehyde / furfuraldehyde. The polymeric Schiff bases were found to form complexes readily with several transition metal ions. The resins were completely soluble in dimethyl sulphoxide, tetrahydrofuran, partially soluble in CHCl , CCl , and insoluble in water. On formation of the 3 4 polychelate with transition metal ions such as Cu(II) and Ni(II), the solubility sharply decreased. The Schiff bases, resins 1 1 3
and the polychelates were characterized by FTIR, FT H-NMR, C-NMR and XRD studies, and thermal analyses like TGA and DSC. From FTIR studies the phenolic oxygen and the imine nitrogen of the resins were found to be the coordination 1 sites. The H-NMR data indicated the presence of bridging methylene and terminal methylol functions in the formaldehydecondensed Schiff base. The thermal stability of the resins and the polychelates was compared by analysing TG data which provided the various kinetic parameters like activation energy, frequency factor and entropy changes associated with the thermal decomposition. The DSC and XRD data indicated that the incorporation of the metal ions significantly enhanced the degree of crystallinity. The adsorption characteristics of the resins towards Cu(II) and Ni(II) in dilute aqueous solutions were followed spectrophotometrically. Cu(II) was seen to undergo preferential adsorption in a mixture of Cu(II) and Ni(II). The effects of contact time, pH, temperature, the size of the sorbents and the concentration of the metal ions in solution on the metal uptake behavior of the resins were studied.
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Phenolic Schiff bases derived from o-, m-, and p-hydroxybenzaldehydes and 4, 4Ј-diaminodiphenyl ether were subjected to polycondensation reaction with formaldehyde. The resins were found to form polychelates readily with several metal ions. The materials were characterized by elemental analysis, GPC
Schiff bases of hydroxy benzaldehydes with aliphatic and aromatic 1,2-diamines were resinified in HCHO in alkaline media. These resins were found to form complexes readily with Cu(II), Co(II), and Ni(I1). The materials were characterized by infrared, 'H-NMR, UV-visible (UV-vis) spectral studies, and
The diazonium salts of aniline and 4,4Ј-diaminodiphenylmethane coupled with phenol and resorcinol were condensed with formaldehyde in alkaline media to yield polymeric resins. These polymers were found to readily react with metal ions like Cu 2ϩ and UO 2 2ϩ , forming polychelates. The azodyes, resin