A glycidyl methacrylate-based resin with pendant urea groups as a high capacity mercury specific sorbent
Loading...
Date
2003
Authors
Bıçak, Niyazi
Sherrington, David C.
Şungur, Şana Kutun
Tan, Nükhet
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier Science Bv
Open Access Color
Green Open Access
Yes
OpenAIRE Downloads
OpenAIRE Views
Publicly Funded
No
Abstract
Polymer-supported pendant urea groups have been demonstrated to be very efficient in selective removal of mercuric ions from aqueous solutions. Methyl methacrylate (0.5 mol)-glycidyl methacrylate (0.4 mol)-divinylbenzene (0.1 mol) terpolymer beads have been prepared by suspension polymerisation. Urea functions have been incorporated into the bead polymer (210-420 mum) via a two-step modification of the epoxy groups involving firstly reaction with excess of triethylenetetramine followed by acidic isocyanate. The resulting polymer resin has a urea group loading of 7.8 mmol g(-1) and shows excellent mercury binding capacity > 6.7 mmol g(-1) even in the presence of excess chloride ions. The mercury sorption is strictly selective and Ca(II) Mg(II) Zn(H) Pb(II) Fe(II) and Cd(II) ions (0.2-0.3 M) do not give rise to any interference. The mercury can be recovered from loaded beads using hot acetic acid thereby regenerating the polymer. Recovered samples can be recycled more than 20 times without loss of activity as a result of the hydrolytic stability of the urea group in acetic acid. (C) 2002 Elsevier Science B.V. All rights reserved.
Description
Keywords
Selective mercury removal, Polymer supported urea, Chemistry, Polymer supported urea, Selective mercury removal, 540
Fields of Science
02 engineering and technology, 0210 nano-technology, 01 natural sciences, 0104 chemical sciences
Citation
WoS Q
Q1
Scopus Q
Q2

OpenCitations Citation Count
52
Source
Reactive and Functional Polymers
Volume
54
Issue
1-3
Start Page
141
End Page
147
PlumX Metrics
Citations
CrossRef : 43
Scopus : 60
Captures
Mendeley Readers : 15
SCOPUS™ Citations
60
checked on Feb 12, 2026
Web of Science™ Citations
56
checked on Feb 12, 2026
Page Views
6
checked on Feb 12, 2026
Downloads
75
checked on Feb 12, 2026
Google Scholar™


