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---→
hv(UV ) TiO
2
(e−, h+) (19)
+ Electron beam irradiation Advance Oxidation
TiO
2
(h+
VB
) + H
2
O
---→
hv(UV ) TiO
2
+H+ + OH (20) O
3 ∕ Ultrasonic H
2
Advance Oxidation O
2
∕ UV Advance Oxidation
Table 35: Advanced oxidation processes (Kdasi, et al., 2004) [20].
TiO
2
(h+
VB
) + HO−
---→
hv(UV ) TiO
2 + OH O
2
(21)
+ TiO
2
(e−
CB
)
---→
hv(UV ) TiO
2
+O
2
− (22)
used alone. A 99% decolourization was noted when H
2
in 30 min for reactive yellow 15 dye
OH + dye
---→ hv(UV ) End product TiO
2
---→
hv(UV ) End
product (23) initial absorbance value O
2
was used alongside fenton’s reagent, the dye’s being 2430 at 415nm [106]. Arslan et al. [107] stated that UV catalyzed by H
2
(h+
VB
) + dye
(24)
used alone, colour from while a dye bath H
2
O
2 which /O 3
was includes O found 2
is more efficient than ozone when to be the quickest in removing a mixture of seven dyes and has
Where:
TiO
2 (
an absorbance of 0.47 in 40 folds at 600 nm.
Treatment with H
2
Volume 5 • Issue 1 • 1000182 h+
VB)
- Valence-band holes
TiO
2 (
e-
CB)
- Conduction-band Electrons
H alkalis, the 2 O
degradation 2
alone but the as combination known of organic was O 2 and not compounds of H found UV: 2 O
2 /UV Oxidation to [20]. was be effective found Wang of textile to et on be al. very both [32], effluent effective acids recorded
using and in
that structure H
2
O
2 of /UV azo treatment is capable of destroying the chromophore resulted in the Upon irradiation by UV, the electrons on the
surface of the semiconductor gets excited to the conduction band forming positive holes in the valance band (Equation 19). The
valance band holes thus formed are good oxidizers; they have the potential to oxidise water or OH ions into OH radicals as
shown in Equations 20 and 21. The dyes complete and that decolourization UV irradiation of in sulphonated the presence azo of
H
and
2
O
2
conduction band electrons on the other hand act as reducers (Equation 22). Chain termination would occur as shown in Equations
23and 24. anthraquinone dyes. The production of OHo processes is as follows [108].
radicals in the H
2
O
2
/UV
Oxidation of TiO
2
H
2
/UV is suggested to have a larger advantage over
---→
hv(UV ) 2OHo (13)
H to 2
O 385 2
/UV, nm which this is because is greater titanium than that dioxide absorbed is found by H 2
to
absorb light up O
2 H
2
O
2
[112].
O
2
+ OHo
---→
hv(UV ) H
2
O + HO
2 H
2
O
2
+ HO
2
---→
hv(UV ) OHo + H
2
O + O
2
(14)
(15)
Halmann et al. [111], reported that the dye Acid Orange 5 which is normally found in effluents in concentrations of 10-4 to 10-6
M can be completely degraded using black-light mercury lamp as a UV radiation OHo + OHo
---→
hv(UV ) H
2
O
2 OH- + H+
---→
hv(UV ) H
2 O (16)
source. Koprivanac et al. [113] reported a 71% reduction in colour when the effluent (17)
[114], stated that was treated at a highest of 70.6% a pH of reduction 3 under UV/TiO
and a lowest 2
. Liu et of 44.3% al.
HO
2
+ HO
2
o
---→
hv(UV ) H
2
O
2
+ O
2
(18)
Equation (13) shows the chain initiation processes as the hydrogen
reduction of acid yellow 17 was achieved when the effluent was treated under UV/TiO
2
peroxide present in the effluent is split into two OHo radicals. Equations (14) and (15) show the reaction between the OHo
radicals formed and the hydrogen peroxide present in the system which results in chain propagation. Equations (16), (17) and
(18) show the chain termination mechanism [108].
The decolourization efficiencies of the H
2
.
Toxicity Measurement Parameters: The by-product produced may be more harmful than the original organic compound
[115]. Hydroxyl functional groups and aldehydes are found to be the usual by- product after destruction of azo dyes [116].
Therefore, it is important to analyse the intermediates produced before letting the effluent into the environment [117].
By-products of dyes with simple structure could
found to increase as the concentration effluent [109]. Kdasi et al. [20] found of that H
O
99.9% 2 O 2 /UV 2
was decolourization combination increased were in the of
be identified by simple procedures. For dyes with extremely complex structures, identification can be carried out using
chromatographic technologies, HPLC, GC techniques [115]. Further tests due to remazol brilliant blue dye was obtained when a
of 12.5 mL L-1 was used and temperature did not H
play 2 O
2
any concentration significant
degradation such as Chemical Oxygen Demand (COD) analysis could be done on the treated effluents to note down the amount
of chemicals role in the removal of colour. Mahmoud et al. [98] stated that excess
present in the effluent. concentration problems due to
of their H
2
O
property 2
added to the effluent was not found to cause to react with the OHo radicals resulting in the formation of H
2
Oand O
2
.
Lidia et al. [118], reported a COD removal of 10% when dyes were treated with 0.5g dm-3 of ozone at a pH 8. AO
3
dispersed
Some of the advantages of UV/H
2
/
UV treatment of textile effluents was found the property of developing any chemical O
2 sludge, combination (b) it is are: effective (a) it lacks in the
A COD reduction of 50 to be far more effective mg/L from 400 mg/L was than achieved O
3
treatment. in 30 minutes [119]. Arslan and Balcioglu [25], noted down 67.58% COD removal of phenolic compounds [100],
chlorinated compounds and
reduction in Turquoise Blue G133 and 80.36%
reduction in Remazol chlorophenols [110], from effluents, (c) UV acts as a disinfectant and (d) it is effective in removal of TOC,
80-82% removal efficiency after
Black B dye when treated with UV/TiO
2
.
J Chem Eng Process Technol ISSN: 2157-7048 JCEPT, an open access journal
Citation: Ghaly AE, Ananthashankar R, Alhattab M, Ramakrishnan VV (2014) Production, Characterization and Treatment of
Textile Effluents:
A Critical Review. J Chem Eng Process Technol 5: 182. doi: 10.4172/2157-7048.1000182
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