Environmental Engineering Reference
In-Depth Information
Table 11.5 Summary of alumina-based porous materials applied for water treatment.
Alumina-
Compound
Pore
Size
(nm)
Surface
Area
(m 2 /g)
Target
Comp'd
Results
Ref.
Mesoporous
Alumina
As(V): 121 mg of As(V)/g
As(III): 47 mg of As(III)/g
(Kim et
al., 2004)
3.5
307
Arsenic
Aminated
Mesoporous
Alumina
Copper ion is removed by > 95%
from 10 ppm solution
(Rengara
j et al.,
2004)
Cu 2+
3.9
299
Cd's K d ( m 3 /g) 1.0 x 10 -2
Se(III)'s K d (m 3 /g): 1.1 x 10 -3
(Papelis
et al.,
1995)
Transition
Aluminas
Cd and
Se(II)
2 <
200
TCE conversion starts from 5% at
443 K and rises to very high values
in the 673-873 K ranges, with the
CO 2 yield being 99% at the same
temperature ranges. HCl and Cl 2
are the other main products with
little halogenated VOC
intermediates
-Alumina-
Supported
Manganese
Oxide
(Tseng et
al., 2003)
11.5
128
TCE
At 443 K and 1.5 MPa, 65% of
total organic carbon (TOC) and
99% color were removed after 3 h
treatment
(Zhang
and
Chuang,
1999)
Pd-Pt-
Ce/Alumina
Catalyst
TOC
and
Color
-
102
Using a post-hydrolysis method, Kim et al. (2004) have developed mesoporous
alumina (MA) with a high surface area of 307 m 2 /g, a uniform pore size of 3.5 nm and a
sponge like interlinked pore system. The resulting MA is insoluble and stable within the
pH range of 37. The maximum uptake of As(V) by MA is found to be 7 times higher
[121 mg of As(V)/g and 47 mg of As(III)/g] than that of the conventional AA; the
adsorption kinetics is also rapid, with complete adsorption in < 5 h, as compared to the
conventional AA (about 2 d to reach half of the equilibrium value). A desorption study
using sodium hydroxide solutions (0.011 M) is conducted, and more than 85% of the
arsenic adsorbed to the MA is desorbed in less than 1 h. These studies show that MA
with a wide surface area, a uniform pore size, and an interlinked pore system can be
used as an efficient adsorbent for the removal of arsenic (Kim et al., 2004).
Shin et al. (2004) tested aluminum-impregnated mesoporous adsorbents to
remove phosphate in water. To understand the effect of surface properties on the
adsorption behavior of phosphate, the surface structure of the materials was investigated
with X-ray diffraction (XRD), a N 2 adsorption-desorption technique, FTIR, and X-ray
photoelectron spectroscopy (XPS). The mesoporous materials were loaded with Al
components by reaction with surface silanol groups. In the adsorption test, the Al-
 
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