Characterization of metal ion interactions with chitosan by X-ray photoelectron spectroscopy

Citation
L. Dambies et al., Characterization of metal ion interactions with chitosan by X-ray photoelectron spectroscopy, COLL SURF A, 177(2-3), 2001, pp. 203-214
Citations number
41
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
ISSN journal
09277757 → ACNP
Volume
177
Issue
2-3
Year of publication
2001
Pages
203 - 214
Database
ISI
SICI code
0927-7757(20010228)177:2-3<203:COMIIW>2.0.ZU;2-S
Abstract
X-ray photoelectron spectroscopy (XPS) is employed to study chemical intera ctions between three metal ions Cu(II), Mo(VI), and Cr(VI) - and chitosan, a natural biopolymer extracted from crab shells. Three forms of chitosan ar e used - flakes, beads, and modified beads obtained by glutaraldehyde cross -linking. XPS provides identification of the sorption sites involved in the accumulation of metals, as well as the forms of species sorbed on the biop olymer. It is found that sorption occurs on amine functional groups for all the three metals. With copper, the sorption step is not followed by reduct ion of the metal. More complex phenomena are involved in molybdate removal. A partial reduction (about 20-25% of the total molybdenum content) occurs with chitosan beads and flakes. The distribution of reduced Mo(V) on the su rface of the sorbent differs from that in the bulk of the sorbent for raw c hitosan beads. while the glutaraldehyde cross-linking allows uniform distri bution of reduced Mo(V) throughout the sorbent. The difference between thes e two forms of chitosan can be related to a complementary photoreduction st ep occurring on the surface of the biopolymer. For chromium, a similar tren d with molybdenum is followed but to a greater extent; with cross-linked so rbents all chromate previously sorbed is reduced to Cr(III), while with raw chitosan beads Cr(VI) reduction does not exceed 60%. (C) 2001 Elsevier Sci ence B.V. All rights reserved.