BIOSORPTION OF Pb2+, Cd2+, & Ni2+ FROM WATERS BY ...
BIOSORPTION OF Pb2+, Cd2+, & Ni2+ FROM WATERS BY ...
BIOSORPTION OF Pb2+, Cd2+, & Ni2+ FROM WATERS BY ...
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mechanism on the cell surface after the interaction between the metal and active<br />
groups occurs. This type of mechanism is only valid for Ca, Mg, Cd, Zn, Cu, and Hg<br />
(Vegliò 1997). Organic acids such as citric, oxalic, gluonic, fumaric, lactic and malic<br />
acids can be be produced by micro-organisms, and chelation of toxic metals with<br />
these acids forms metallo-organic molecules. Carboxyl groups found in microbial<br />
polysaccahrides and other polymers may give complexation reaction with metals.<br />
It is clear to be understanding that biosorption mechanisms can also take place<br />
at the same time.<br />
1.4.2. Factors Affecting Biosorption<br />
In order to understand the quality of the biosorption process and to design the<br />
system for the removal of contaminants, we need to evaluate the effect of factors<br />
which influences the performance of biosorption. The following factors are thougth to<br />
be responsible for biosorption:<br />
1. When the temperature of the sorption media is in the range of 20-35 0 C the<br />
biosorption process is not affected by temperature (Aksu, et al. 1992).<br />
However, if the increment in the temperature reduces the sorption capacity of<br />
biomass (Aksu 2001).<br />
2. The major challenging factor for the biosorptive process is pH seems to be the<br />
most important parameter in the biosorptive process. Since, it influences not<br />
only the solution chemistry of the metals but also the activity of the<br />
functional groups in the biomass and the competition of metallic ions. Table<br />
1.2 shows the functional groups responsible for the binding of metal and their<br />
acidity constants. These groups create a negatively charged surface at above<br />
the isoelectronic point of the biomass and electrostatic attractions among<br />
metals and the cell surface is involved in the biosorption process. At low pH<br />
values below isoelectronic point, the functional groups are protonated surface<br />
charge. This comes to a conclusion with lower metal uptake when the metal is<br />
in the cationic form such as Pb 2+ , this is due to blocking of functional groups<br />
responsible for the metal uptake. However, in the case of Cr(VI) which is<br />
anionic in nature, it can bind at lower pH values , that is the surface charge of<br />
the cell wall is positive in nature.<br />
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