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Determination of surface properties of iron hydroxide-coated alumina adsorbent prepared for removal of arsenic from drinking water
A novel type adsorbent was prepared by in situ precipitation of Fe(OH) 3 on the surface of activated Al 2O 3 as a support material. The iron content of the adsorbent was 0.31 ± 0.003 % m/m (56.1 mmol/g); its mechanical and chemical stability proved to be appropriate in solutions. The total capacit...
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Published in: | Journal of colloid and interface science 2005-04, Vol.284 (1), p.71-77 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A novel type adsorbent was prepared by in situ precipitation of Fe(OH)
3 on the surface of activated Al
2O
3 as a support material. The iron content of the adsorbent was
0.31
±
0.003
%
m/m
(56.1 mmol/g); its mechanical and chemical stability proved to be appropriate in solutions. The total capacity of the adsorbent was 0.12 mmol/g, and the pH of zero point of charge, pH
zpc
=
6.9
±
0.3
. Depending on the pH of solutions, the adsorbent can be used for binding of both anions and cations, if pH
eq
<
pH
zpc anions are sorbed on the surface of adsorbent (S) through {S
OH
2
+
} and {S
OH} groups. A graphical method was used for the determination of pH
iep (isoelectric points) of the adsorbent and values of pH
iep
=
6.1
±
0.3
for As(III) and pH
iep
=
8.0
±
0.3
for As(V) ions were found. The amount of surface charged groups (
Q) was about zero within the a pH range of 6.5–8.6, due to the practically neutral surface formed on the adsorption of As(V) ions. At acidic pH (pH 4.7),
Q
=
0.19
mol
/
kg
was obtained. The adsorption of arsenate and arsenite ions from solutions of 0.1–0.4 mmol/L was represented by Langmuir-type isotherms. A great advantage of the adsorbent is that it can be used in adsorption columns, and low waste technology for removal of arsenic from drinking water can be developed. |
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ISSN: | 0021-9797 1095-7103 |
DOI: | 10.1016/j.jcis.2004.10.032 |