V. Gutanu et al., IONIC POLYMERS .3. SORPTION OF FE(III) IONS ON NEW CROSS-LINKED IONICPOLYMERS BASED ON 4-VINYLPYRIDINE - DIVINYLBENZENE COPOLYMERS, Journal of applied polymer science, 59(9), 1996, pp. 1371-1377
Copolymers of 4-vinylpyridine : divinylbenzene with various degrees of
crosslinking have been obtained as precursors for ionic polymers. To
this end, addition reactions of the 4-vinylpyridine : 8% divinylbenzen
e copolymer to electrophylic ethylenic compounds, such as acrylamide,
acrylonitrile, and methyl vinyl ketone in the presence of HCl have bee
n performed; the resulting ionic polymers contain, besides ammonium qu
aternary groups, other functional groups such as amide, nitrile, and k
etone. The quantitative iron retention from aqueous Fe-2(SO4)(3) solut
ions was determined photocolorimetrically for both 4-vinylpyridine : d
ivinylbenzene copolymers and the synthesized ionic polymers. IR and Mo
ssbauer spectroscopy were used to determine the state of the Fe(III) i
ons in the tridimensional networks. As expected, in 4-vinylpyridine :
divinylbenzene copolymers, Fe(III) ions are retained by nitrogen atoms
-Fe(III) complexes. The electronic state of metal ions hardly depends
on the crosslinking degree. In the ionic polymers, the Fe(III) ions ar
e retained through ionic exchange as the R(4)N(+)[Fe-3(SO4)(2)(OH)(6)]
(-) complex anion. The functional amide, nitrile, and ketone groups, a
lthough containing atoms able to form donor-acceptor bonds, do not tak
e part in the complexation. (C) 1996 John Wiley & Sons, Inc.