Potential of protonated alginate beads for heavy metals uptake

被引:93
作者
Ibáñez, JP
Umetsu, Y
机构
[1] Arturo Prat Univ, Dept Met, Iquique, Chile
[2] Tohoku Univ, Inst Adv Mat Proc, Aoba Ku, Sendai, Miyagi 9808577, Japan
关键词
alginite beads; protonation; heavy metal ions;
D O I
10.1016/S0304-386X(02)00012-9
中图分类号
TF [冶金工业];
学科分类号
0806 ;
摘要
The potential for uptake of several heavy metal ions by alginate in the form of protonated beads was investigated at 25 degreesC. The morphological characteristics of the beads and their behavior in aqueous solutions were examined as well. The ability of protonated alginate beads to remove heavy metal ions from dilute aqueous solutions was demonstrated. The uptake of trivalent chromium, copper, zinc, nickel and cobalt was found to be about 75, 77, 46, 43 and 3 5 mg per g of beads, respectively. The uptake increased with solution pH and acid concentration for protonation, and with decreasing ionic strength. The cross-linking agents, Ba and Ca, were not released during uptake, and protons were liberated instead. Therefore, the uptake was associated with ion exchange between protons of the free carboxylic functional groups of the alginate and metal ions from the solutions. EPMA-EDX analyses showed that heavy metals were uniformly distributed throughout the surface (external and internal) of the beads, indicating that protonated dry alginate beads can be considered as porous ion exchangers. Observation of protonated dry alginate beads by scanning electron microscopy (SEM) showed a corrugated surface having a uniform distribution of regular nodules and cavities. A mean diameter of about 1.0 mm was obtained for these beads. They were found to have chemical and structural stability in acidic and slightly acidic environments. Bead forming reaction with Ba or Ca makes it possible to use alginate as sorbent for heavy metal ions in extremely dilute aqueous solutions. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:89 / 99
页数:11
相关论文
共 27 条
[1]  
ASHLEY NV, 1990, J CHEM TECHNOL BIOT, V49, P381
[2]   STRUCTURAL COMPONENTS OF ALGINIC ACID .2. CRYSTALLINE-STRUCTURE OF POLY-ALPHA-L-GULURONIC ACID - RESULTS OF X-RAY-DIFFRACTION AND POLARIZED INFRARED STUDIES [J].
ATKINS, EDT ;
NIEDUSZYNSKI, IA ;
PARKER, KD ;
SMOLKO, EE .
BIOPOLYMERS, 1973, 12 (08) :1879-1887
[3]   PHYSICAL STUDIES ON CELL IMMOBILIZATION USING CALCIUM ALGINATE GELS [J].
CHEETHAM, PSJ ;
BLUNT, KW ;
BUCKE, C .
BIOTECHNOLOGY AND BIOENGINEERING, 1979, 21 (12) :2155-2168
[4]   Biosorption of metal ions from aqueous solutions [J].
Chen, JP ;
Yiacoumi, S .
SEPARATION SCIENCE AND TECHNOLOGY, 1997, 32 (1-4) :51-69
[5]   Equilibrium and kinetic studies of copper ion uptake by calcium alginate [J].
Chen, JP ;
Tendeyong, F ;
Yiacoumi, S .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (05) :1433-1439
[6]   Contribution of sulfonate groups and alginate to heavy metal biosorption by the dry biomass of Sargassum fluitans [J].
Fourest, E ;
Volesky, B .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (01) :277-282
[7]   CALCIUM ALGINATE BEAD MANUFACTURE - WITH AND WITHOUT IMMOBILIZED YEAST - DROP FORMATION AT A 2-FLUID NOZZLE [J].
GILSON, CD ;
THOMAS, A .
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 1995, 62 (03) :227-232
[8]   BIOLOGICAL INTERACTIONS BETWEEN POLYSACCHARIDES AND DIVALENT CATIONS - EGG-BOX MODEL [J].
GRANT, GT ;
MORRIS, ER ;
REES, DA ;
SMITH, PJC ;
THOM, D .
FEBS LETTERS, 1973, 32 (01) :195-198
[9]   EFFECT OF DIVALENT METALS ON PROPERTIES OF ALGINATE SOLUTIONS .2. COMPARISON OF DIFFERENT METAL IONS [J].
HAUG, A ;
SMIDSROD, O .
ACTA CHEMICA SCANDINAVICA, 1965, 19 (02) :341-&
[10]   ALKALINE DEGRADATION OF ALGINATE [J].
HAUG, A ;
LARSEN, B ;
SMIDSROD, O .
ACTA CHEMICA SCANDINAVICA, 1967, 21 (10) :2859-&