『Abstract
In this study, an iron-zirconium binary oxide with a molar ratio
of 4:1 was synthesized by a simple coprecipitation process for
removal of phosphate from water. The effects of contact time,
initial concentration of phosphate solution, temperature, pH of
solution, and ionic strength on the efficiency of phosphate removal
were investigated. The adsorption data fitted well to the Langmuir
model with the maximum P adsorption capacity estimated of 24.9
mg P/g at pH 6.5 and 33.4 mg P/g at pH 5.5. The phosphate adsorption
was pH dependent, decreasing with an increase in pH value. The
presence of Cl-1, SO42-,
and CO32- had little adverse effect
on phosphate removal. A desorbability of approximately 53% was
observed with 0.5M NaOH, indicating a relatively strong bonding
between the adsorbed PO43- and
the sorptive sites on the surface of the adsorbent. The phosphate
uptake was mainly achieved through the replacement of surface
hydroxyl groups by the phosphate species and formation of inner-sphere
surface complexes at the water/oxide interface. Due to its relatively
high adsorption capacity, high selectivity and low cost, this
Fe-Zr binary oxide is a very promising candidate for the removal
of phosphate ions from wastewater.
Keywords: Fe-Zr binary oxide; Phosphate removal; Adsorption; Mechanism』
1. Introduction
2. Materials and methods
2.1. Materials
2.2. Preparation of Fe-Zr binary oxide
2.3. Batch adsorption tests
2.3.1. Adsorption kinetics
2.3.2. Effect of pH and ionic strength
2.3.3. Adsorption isotherm
2.3.4. Effect of coexisting anions
2.3.5. Desorption of phosphate
2.3.6. Characterization of adsorbent before and after phosphate
adsorption
3. Results and discussion
3.1. Adsorbent properties
3.2. Adsorption kinetics
3.3. Adsorption isotherm
3.4. Effect of pH and ionic strength on phosphate uptake
3.5. Effect of coexisting anions
3.6. Desorption of phosphate
3.7. Zeta potential measurement and FTIR analysis
4. Conclusions
Acknowledgment
References