Synthesis, characterization, and metal-ion uptake studies of chelating resins derived from formaldehyde-condensed azodyes of aniline and 4,4 '-diaminodiphenylmethane coupled with phenol/resorcinol

Citation
S. Samal et al., Synthesis, characterization, and metal-ion uptake studies of chelating resins derived from formaldehyde-condensed azodyes of aniline and 4,4 '-diaminodiphenylmethane coupled with phenol/resorcinol, J APPL POLY, 77(14), 2000, pp. 3128-3141
Citations number
31
Categorie Soggetti
Organic Chemistry/Polymer Science","Material Science & Engineering
Journal title
JOURNAL OF APPLIED POLYMER SCIENCE
ISSN journal
00218995 → ACNP
Volume
77
Issue
14
Year of publication
2000
Pages
3128 - 3141
Database
ISI
SICI code
0021-8995(20000929)77:14<3128:SCAMUS>2.0.ZU;2-N
Abstract
The diazonium salts of aniline and 4,4'-diaminodiphenylmethane coupled with phenol and resorcinol were condensed with formaldehyde in alkaline media t o yield polymeric resins. These polymers were found to readily react with m etal ions like Cu2+ and UO22+, forming polychelates. The azodyes, resins, a nd polychelates were characterized by several instrumental techniques such as elemental analysis, FTIR, H-1-NMR, GPC, XRD, TG-DTG, and DSC studies. Th e chelating capacity of the resins toward Cu2+ and UO22+ ions was studied b y spectrophotometry. The extent of metal loading of the resins was studied by varying the time of contact, metal-ion concentration, and pH of the reac tion medium. The alkali and alkaline earth metal ions had little effect on the metal-ion uptake behavior of the resins. The resin derived from the azo dye of 4,4'-diaminodiphenylmethane was found to be more efficient in removi ng the metal ions from solution than were the resins from aniline. The opti mum conditions for effective separation of Cu2+ from UO22+ were determined. (C) 2000 John Wiley & Sons, Inc.