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Research Inventy: International Journal Of Engineering And Science
Vol.5, Issue 2 (February 2015), PP 50-55
Issn (e): 2278-4721, Issn (p):2319-6483, www.researchinventy.com
50
Investigation on the Effect of TiO2 and H2O2 for the Treatment of
Inorganic Carbon Present in Seawater
Hasna Al Jabri*1
, Alaa Al-Hudaifi1
, Shaik Feroz1
, Fouzul Ameer Marikar2
,
Mahad Baawain2
1
Caledonian Center for Creativity and Innovation, Caledonian College of Engineering, Sultanate of Oman.
2
College of Engineering, Sultan Qaboos University, Sultanate of Oman.
ABSTRACT: Sodium hypochlorite (NaClO) is regularly used as a disinfectant or a bleaching agent because of
its high efficiency against many bacteria and viruses present in seawater along with its cheaper cost. Now a
days, with the increase in the environmental concerns concerning the use of chlorination for the disinfection or
bleaching of treated water related to the formation of potentially harmful chloro-organic by products through
reactions with natural organic matter (NOM), it is preferred to implement a process with environmentally
friendly chemicals for water treatment processes. About This report aim to study the possibility of reducing the
inorganic carbon present in seawater by oxidization reaction of seawater with TiO2 and H2O2. Investigated and
a comparison between thin film method and suspension method with a reactor system in conjunction with a light
concentrating system has been done.
KEYWORDS: Inorganic Carbon, H2O2, Nano photocatalysis, TiO2, Seawater treatment, Solar Energy.
I. INTRODUCTION
Throughout the last years several disinfection technologies have been investigated for drinking waters
and waste waters, but seawater has only been tested recently. Since water quality is an important factor in the
water treatment process, finding an alternative method which is environmentally friendly is important to avoid
the production of toxic waste. Therefore more research is done on advanced oxidation technologies which are
able to produce highly reactive OH radicals to accelerate the degradation rate of seawater contaminations.
Based on Oman Power and Water Procurement’s 7-year statement from 2014 to 2020, water demand is expected
to increase by 6% per year, from 238 million m3
in 2013 to 349 million m3
in 2020 in the northern region.
Where 5.5% per year increase is expected in the Salalah System. Ad Duqm Zone is expecting a high increase of
water demand of 32% for non-industrial and 76% for industrial uses. This high demand expectation is due to Ad
Duqm projects including Ad Duqm airport and the industrial area. Expansion of a number of desalination plants
and additional of new desalination plants to meet the high demand of water expected by 2020 was reported
along with considering the potential of extending the contracts of a major supplying plant. [1]
Nano-scale Photocatalysts has more photocatalytic activity than the normal scale catalyst as it will be having
larger surface area for contacting between the reactants and it’s having a smaller size that will reduce the time
needed for the carrier diffusing out of the photocatalyst pours to the photocatalysts surface. [2]
When light illuminate the surface of the photocatalysts with bandgap energy equal or higher than the
semiconductors bandgap, the semiconductor gets activated by the absorption of photons then the electrons get
excited from the valance bond to the conduction bond resulting in the formation of a positive hole (p+) in the
valance band and an electron (e-) in the conduction band. The positive hole can oxidize the pollutant directly or
oxidize water to form (.
HO) radicals. At the same time, the electron reduces the oxygen adsorbed to the
photocatalyst which prevents the combination of electrons and the positive hole. [3]
The reaction bellow explains the photocatalytic reaction mechanism:
Photocatalyst e-
+ p+
e-
+ O2 O2
-
p+
+ Organics CO2
p+
+ H2O .
HO + H+
.
HO + Organics CO2 [4]
Investigation on the Effect…
51
There are several advantages and disadvantages of choosing suspension photocatalysis. Suspension
process will be having a uniform photocatalyst distribution in the reactor system, higher efficiency because of it
larger surface area and low pressure drop as the suspension particles are well mixed. The process will also
minimize catalyst fouling because the catalyst is continuously removed. Where, the main disadvantage is the
requirement of a Nano filter to separate the catalyst which will increase the cost of the unit. On the other hand,
thin film method is a continuous operation and doesn’t need a separation step after the reaction taking place. But
it has lower light utilization efficiency because the surface area utilized is less than the suspension method. [5] It
was reported that Titanium dioxide is having an energy bandgap of 3.2 eV which is activated by UV
illumination with a wavelength up to 387.5 nm. At the ground level, solar irradiation starts at a wavelength of
about 300 nm. Which results in utilizing 4 to 5% only the solar energy reaching the surface of the earth. [6]. A
number of methods are available for producing hydroxyl radicals. It can be categorized into two categories: non-
photochemical method and photochemical methods. Non-photochemical method includes: ozonation at elevated
pH (> 8.5), Ozone and hydrogen peroxide (O3/H2O2), Ozone and catalyst (O3/CAT), Fenton system (H2O2/Fe2+
).
Photochemical methods includes: ozone-UV radiation (O3/UV), hydrogen peroxide-UV radiation (H2O2/UV),
ozone-hydrogen peroxide-UV radiation (O3/ H2O2/UV), Photo-Fenton and Fenton-like systems, and
photocatalytic oxidation (UV/TiO2). [7]
Table (1) shows Relative oxidation power of some oxidizing species. [7]
Oxidizing Species Relative oxidation power
Chlorine 1.00
Hypochlorous acid 1.10
Permanganate 1.24
Hydrogen peroxide 1.31
Ozone 1.52
Atomic oxygen 1.78
Hydroxyl radical 2.05
Positively charged hole on titanium dioxide, TiO2
+
2.35
A comprehensive research was done on Milli-Q water, Leman Lake water and artificial seawater to observe the
photo-inactivation and reactivation of E.coli. Along with studying the outcome of experimenting dissolved
bicarbonates and NOM as these compounds affect the effectiveness of the treatment methods used. Milli-Q
water should a higher decrease of the bacterial inactivation rate compared to Leman Lake water as a result of the
absence of inorganic ions. Even though there is a high difference in salt concentration Leman Lake water and
seawater but Inactivation rates were similar to each other. [8]
The advanced oxidation processes (AOPs) are presented as treatment of future in disinfection and removal of
contaminants from water. [9] Advanced oxidation processes represent a group of techniques used for the
treatment of water characterized by the generation of radicals, such as the hydroxyl radical (OHº) and may be an
alternative to chlorine disinfection. [10]
A Study of Hydrogen Peroxide electro-generation in seawater was done and the result showed that in the
absence of a reducing substrate, the fast production rate of active chlorine leads to total depletion of H2O2. And
the simultaneous anodic production of oxidizing species, mainly active chlorine, severely affects the stability of
hydrogen peroxide due to the chemical reaction between these species. [11] It was found that in order to
improve the elimination efficiency an oxidant could be added during UV irradiation which absorbs the UV light
by itself and reacts with water to form a highly reactive OH radicals. Hydrogen peroxide (H2O2) and ozone are
the commonly used oxidants. It was absorbed during the experiments that the absorbance efficiency of H2O2 is
reliant on its concentration. The higher the concentration of H2O2, the better the performance of the water
treatment system. [12] It was observed that the oxidation rate of nanomolar Fe(II) with H2O2 is a function of pH,
temperature and the concentration of HCO3
-
and H2O2. And FeOH+
is the most important iron species
controlling the Fe(II) oxidation with H2O2 in the pH range of natural seawater systems. [13]
As shown in fig (1), using a concentrated light system that reflects the solar light onto the photocatalytic reactor
by a reflecting surface is more desired because it will require a smaller reactor volume, it operates at a higher
flow rate, better mass transfer rates, and it can be even operated under cloudy conditions. [14-15]
Investigation on the Effect…
52
Figure 1: a parabolic shaped light reflecting
II. MATERIALS & METHODS
Thin Film Method
a- Material
Seawater was collected 1 km from Al Athibah Beach, Oman. Aeroxide P25 was obtained from Evonik
Industries, 35% Hydrogen Peroxide from The Merck Group, and PVA from Oman Textile Mills Company
L.L.C.
b- Preparation of Coating Solutions
Coating Solution: 5 grams of PVA and 2.2 grams of TiO2 were dissolved in 60ml of water, 30ml of ethanol, 6ml
of acetic acid and 4ml of ethylene glycol. The solution was left for stirring overnight.
c- Coating of Glass Tube
Glass tube is coated with TiO2 thin film by passing the dispersed TiO2 in the inner surface of the tube. The tube
is allowed to dry and then calcinated at 400°C for about 1 hour.
Fig 2 represents the reactor system configuration. Seawater from the system tank was pumped to the thin film
coated reactor using peristaltic pump, where the photo catalysis is activated by sunlight and oxidation reaction
takes place.
Figure 2: Schematic of the Thin Film Experimental Set-up
The tubular photo reactor is 1 meter long with an outer diameter of 2 cm. The system glass tank holds 1.5 litter
of seawater water which is continuously re-circulated through the tubular reactor.
Suspension Method
Fig 3 represents the reactor system configuration. The seawater along with photo catalyst was fed to the reactor
system using peristaltic pump, where the photocatalysis is activated by sunlight. Oxidation reaction takes places
which lowers poisonousness inorganic matter in the contaminated seawater.
Figure 3: Schematic of the Suspension Experimental Set-up
Investigation on the Effect…
53
Two tubular photo reactors were connected with a silicon tube. Each tube is 1 meter long with an outer diameter
of 2 cm. The system glass tank holds 2 litter of seawater water along with 3 gram of the photo catalyst which is
mixed by a magnetic stirrer. The solution is then continuously re-circulated through the tubular reactor.
III. RESULT AND DISCUSSION
Inorganic Carbon was measured with Total Organic Carbon Analyzer (TOC-L series) from Shimadzu
Corporation.
a- Thin Film Method
Polyvinyl alcohol was used as a solution thickener and a binder to enhance the chemical bonding of TiO2 to the
inner surface of the glass tube. The transparent coated layers of TiO2 was stable, very resistance and strongly
stick on the inner surface of the tube after calcination.
The glass tubes were first illuminated under solar irradiation for 1 hour before it is fitted to the experimental
setup. Then the photocatalytic reaction took place at a UV Index of 6 to 8.
Table (2) shows seawater analysis with coated tubular photoreactor with TiO2. A slight decrease was noticed in
the inorganic carbon value with time. And fig (4) shows the variation in inorganic carbon during photocatalytic
reaction of TiO2 with seawater.
TABLE (2): Seawater analysis with coated tubular photoreactor.
Time 0hr 1hr 2hr 3hr 4hr
UV Index - 6 6 8 8
Temperature ºC - 31 32 34 32
IC (ppm) 25.83 25.65 25.26 25.15 25.05
Figure (4): Variation in In-Organic Carbon during photocatalytic reaction of TiO2 with seawater
Table (3) shows seawater analysis with coated tubular photoreactor with TiO2 alone with H2O2. The decrease in
inorganic carbon value is more when combining TiO2 with H2O2 compared to TiO2 coating alone. Fig (5) shows
the variation in inorganic carbon during photocatalytic reaction of TiO2 along with H2O2.
TABLE (3): Seawater analysis of coated tubular photoreactor with H2O2.
Time 0hr 1hr 2hr 3hr 4hr
UV Index - 7 8 8 6
Temperature ºC - 27 29 29 28
IC (ppm) 25.83 24.24 23.33 21.93 21.66
Investigation on the Effect…
54
Figure (5): Variation in In-Organic Carbon during photocatalytic reaction of TiO2 and H2O2 with seawater
b- Suspension Method
The reaction was carried out for 5 hours continuously and a sample of the treated water was collected every 60
min. The samples were not filtered but it was allowed to settle down overnight water analysis is done
Table (4) shows seawater analysis with suspended photocatalysis of TiO2. It is observed that the decrease in
inorganic carbon value is much more is suspension method compared to thin film method. And fig (6) shows the
variation in inorganic carbon during photocatalytic reaction of TiO2 in suspension.
TABLE (4): Seawater analysis with suspended photocatalysis.
Time 0hr 1hr 2hr 3hr 4hr 5hr
UV Index - 5 6 7 6 5
Temperature ºC - 23 23 23 23 23
IC (ppm) 26.2 23.02 22.5 22.14 22.14 21.43
Figure (6): Variation in In-Organic Carbon during photocatalytic reaction of TiO2 in suspension with seawater
Table (5) shows seawater analysis with suspended photocatalysis of TiO2. It is spotted that there is a significant
decrease in inorganic carbon value of seawater with time. Fig (7) shows the variation in inorganic carbon during
photocatalytic reaction of TiO2 in suspension.
TABLE (5): Seawater analysis of suspended photocatalysis with H2O2.
Time 0hr 1hr 2hr 3hr 4hr 5hr
UV Index - 4 5 6 7 6
Temperature ºC - 22 24 25 24 24
IC (ppm) 26.2 21.18 20.98 20.74 18.66 1.084
Investigation on the Effect…
55
Figure (7): Variation in In-Organic Carbon during photocatalytic reaction of TiO2 and H2O2 in suspension with
seawater
IV. CONCLUSION
Oman is having high sunlight intensity which makes the utilization of solar photocatalysis an environmentally
and sustainable process. Experimental investigations were carried out in an immobilized thin film Nano photo
catalyst as well as suspension mode. The degradation of inorganic compounds present in seawater was studied.
The following conclusions were drawn:
 Nano TiO2 photo catalyst thin film inside the glass tube remains stable with a strong resistance.
 Reduction of Inorganic carbon present in seawater after photocatalytic reaction with TiO2.
 Reduction of IC was slightly more in the presence of hydrogen peroxide.
 A significate reduction of IC was obtained in suspension method with the addition of hydrogen peroxide.
V. ACKNOWLEDGMENT
The authors would like to acknowledge the financial support received from The Research Council, Oman
through grant number 83 (ORG/EI/12/003). The authors also wish to thank Ms. Shamsa Al Saadi for her support
in the laboratory and Mr. Salim for his help in fabricating the experimental set-up in CCE’s Workshop and
finally Mr. Adil Azjoon from SQU Glass Glowing Workshop for sizing of glass tubes.
REFERENCE
[1]. Oman Power and Water Procurement Company (OPWP) 7-Year Statement (2014-2020).
[2]. Z. Meng, and Z. Juan, “Wastewater Treatment by Photocatalytic Oxidization of Nano-ZnO”, Global Environmental Policy, Japan,
No.12, p. 1-9, April, 2008.
[3]. Sarmad Ismail, “Disinfection of wastewater using TiO2 semiconductor photochemistry”, Tampere University of Applied Sciences,
2013.
[4]. Radwan A.Al Rasheed, Water Treatment by Heterogeneous Photocatalysis an Overview, Saline Water Desalination Research Institute
and Saline Water Conversion Corporation (SWCC), Saudi Arabia.
[5]. N. B. Mok, “Photocatalytic Degradation of oily Wastewater: Effect of Catalyst Concentration Load, Irradiation Time and
Temperature”, BSc thesis, Faculty of Chemical & Natural Resources Engineering, University Malaysia Pahang, 2009.
[6]. Bahnemann, D., Bockelmann, D. & Goslich, R. Mechanistic “Studies of water detoxification in illuminated TiO2 suspensions”, Sol.
Energy Mater., 1991, 24, 564–583.
[7]. Melchor Gonzalez-Davila, J. Magdalena Santana-Casian, and Frank J. Millero, “Oxidation of iron (II) nanomolar with H2O2 in
seawater”, Rosenstiel School of Marine and Atmospheric Science, University of Miami,, Geochimica et Cosmochimica Acta, Vol.
69, No. 1, pp. 83-93, 2005.
[8]. D. Rubio a ,b, E. Nebot b, J.F. Casanueva c, C. Pulgarin a, “Comparative effect of simulated solar light, UV, UV/H2O2 and photo-
Fenton treatment (UV-Vis/ H2O2 /Fe2+
, 3+
) in the Escherichia coli inactivation in artificial seawater”, Water Research 47 (2013) 6367
6379.
[9]. Holm, E.R., Stamper, D.M., Brizzolara, R.A., Barnes, L., Deamer, N.N., Burkholder, J.A., “Sonication of bacteria, phytoplankton and
zooplankton: application to treatment of ballast water”, Marine Pollution Bulletin 56, 1201-1208.
[10]. De la Cruz, N., Gimenez, J., Esplugas, S., Grandjean, D., de Alencastro, L.F.,Pulgarin,C., :Degradation of 32 emergent contaminants
by UV and neutral photo-Fenton in domestic wastewater effluent previously treated by activated sludge” Water Research 46, 1947
1957.
[11]. Elisabetta Petrucci, Daniele Montanaro, Luca Di Palma, “A Feasibility Study of Hydrogen Peroxide Electrogeneration in Seawater for
Environmental Remediation”, The Italian Association of Chemical Engineering. ISBN 978-88-95608-19-8; ISSN 1974-9791.
[12]. Muriel Sona, Christine Baus, Heinz-Jürgen Brauch, “UV Irradiation versus combined UV / Hydrogen Peroxide and UV / Ozone
Treatment for the Removal of Persistent Organic Pollutants from Water”, International Conference Ozone and UV, April 3rd 2006.
[13]. Melchor Gonzalez-Davila, J. Magdalena Santana-Casian, and Frank J. Millero, “Oxidation of iron (II) nanomolar with H2O2 in
seawater”, Rosenstiel School of Marine and Atmospheric Science, University of Miami,, Geochimica et Cosmochimica Acta, Vol.
69, No. 1, pp. 83-93, 2005.
[14]. R. Thiruvenkatachari, S. Vigneswaran, Il Shik Moon, “A Review on UV/TiO2 Photocatalytic Oxidation Process”, Korean j. chem.
eng., 25(1), 64-72 2008, vol. 25, p. 64-72, 2008.
[15]. New Technology Demonstration Program, Parabolic-Trough Solar Water Heating. [Online] available:
http://smartenergy.arch.uiuc.edu/pdf/Archive/ParabolicTroughSOlarWaterHeater.pdf

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Investigation on the Effect of TiO2 and H2O2 for the Treatment of Inorganic Carbon Present in Seawater

  • 1. Research Inventy: International Journal Of Engineering And Science Vol.5, Issue 2 (February 2015), PP 50-55 Issn (e): 2278-4721, Issn (p):2319-6483, www.researchinventy.com 50 Investigation on the Effect of TiO2 and H2O2 for the Treatment of Inorganic Carbon Present in Seawater Hasna Al Jabri*1 , Alaa Al-Hudaifi1 , Shaik Feroz1 , Fouzul Ameer Marikar2 , Mahad Baawain2 1 Caledonian Center for Creativity and Innovation, Caledonian College of Engineering, Sultanate of Oman. 2 College of Engineering, Sultan Qaboos University, Sultanate of Oman. ABSTRACT: Sodium hypochlorite (NaClO) is regularly used as a disinfectant or a bleaching agent because of its high efficiency against many bacteria and viruses present in seawater along with its cheaper cost. Now a days, with the increase in the environmental concerns concerning the use of chlorination for the disinfection or bleaching of treated water related to the formation of potentially harmful chloro-organic by products through reactions with natural organic matter (NOM), it is preferred to implement a process with environmentally friendly chemicals for water treatment processes. About This report aim to study the possibility of reducing the inorganic carbon present in seawater by oxidization reaction of seawater with TiO2 and H2O2. Investigated and a comparison between thin film method and suspension method with a reactor system in conjunction with a light concentrating system has been done. KEYWORDS: Inorganic Carbon, H2O2, Nano photocatalysis, TiO2, Seawater treatment, Solar Energy. I. INTRODUCTION Throughout the last years several disinfection technologies have been investigated for drinking waters and waste waters, but seawater has only been tested recently. Since water quality is an important factor in the water treatment process, finding an alternative method which is environmentally friendly is important to avoid the production of toxic waste. Therefore more research is done on advanced oxidation technologies which are able to produce highly reactive OH radicals to accelerate the degradation rate of seawater contaminations. Based on Oman Power and Water Procurement’s 7-year statement from 2014 to 2020, water demand is expected to increase by 6% per year, from 238 million m3 in 2013 to 349 million m3 in 2020 in the northern region. Where 5.5% per year increase is expected in the Salalah System. Ad Duqm Zone is expecting a high increase of water demand of 32% for non-industrial and 76% for industrial uses. This high demand expectation is due to Ad Duqm projects including Ad Duqm airport and the industrial area. Expansion of a number of desalination plants and additional of new desalination plants to meet the high demand of water expected by 2020 was reported along with considering the potential of extending the contracts of a major supplying plant. [1] Nano-scale Photocatalysts has more photocatalytic activity than the normal scale catalyst as it will be having larger surface area for contacting between the reactants and it’s having a smaller size that will reduce the time needed for the carrier diffusing out of the photocatalyst pours to the photocatalysts surface. [2] When light illuminate the surface of the photocatalysts with bandgap energy equal or higher than the semiconductors bandgap, the semiconductor gets activated by the absorption of photons then the electrons get excited from the valance bond to the conduction bond resulting in the formation of a positive hole (p+) in the valance band and an electron (e-) in the conduction band. The positive hole can oxidize the pollutant directly or oxidize water to form (. HO) radicals. At the same time, the electron reduces the oxygen adsorbed to the photocatalyst which prevents the combination of electrons and the positive hole. [3] The reaction bellow explains the photocatalytic reaction mechanism: Photocatalyst e- + p+ e- + O2 O2 - p+ + Organics CO2 p+ + H2O . HO + H+ . HO + Organics CO2 [4]
  • 2. Investigation on the Effect… 51 There are several advantages and disadvantages of choosing suspension photocatalysis. Suspension process will be having a uniform photocatalyst distribution in the reactor system, higher efficiency because of it larger surface area and low pressure drop as the suspension particles are well mixed. The process will also minimize catalyst fouling because the catalyst is continuously removed. Where, the main disadvantage is the requirement of a Nano filter to separate the catalyst which will increase the cost of the unit. On the other hand, thin film method is a continuous operation and doesn’t need a separation step after the reaction taking place. But it has lower light utilization efficiency because the surface area utilized is less than the suspension method. [5] It was reported that Titanium dioxide is having an energy bandgap of 3.2 eV which is activated by UV illumination with a wavelength up to 387.5 nm. At the ground level, solar irradiation starts at a wavelength of about 300 nm. Which results in utilizing 4 to 5% only the solar energy reaching the surface of the earth. [6]. A number of methods are available for producing hydroxyl radicals. It can be categorized into two categories: non- photochemical method and photochemical methods. Non-photochemical method includes: ozonation at elevated pH (> 8.5), Ozone and hydrogen peroxide (O3/H2O2), Ozone and catalyst (O3/CAT), Fenton system (H2O2/Fe2+ ). Photochemical methods includes: ozone-UV radiation (O3/UV), hydrogen peroxide-UV radiation (H2O2/UV), ozone-hydrogen peroxide-UV radiation (O3/ H2O2/UV), Photo-Fenton and Fenton-like systems, and photocatalytic oxidation (UV/TiO2). [7] Table (1) shows Relative oxidation power of some oxidizing species. [7] Oxidizing Species Relative oxidation power Chlorine 1.00 Hypochlorous acid 1.10 Permanganate 1.24 Hydrogen peroxide 1.31 Ozone 1.52 Atomic oxygen 1.78 Hydroxyl radical 2.05 Positively charged hole on titanium dioxide, TiO2 + 2.35 A comprehensive research was done on Milli-Q water, Leman Lake water and artificial seawater to observe the photo-inactivation and reactivation of E.coli. Along with studying the outcome of experimenting dissolved bicarbonates and NOM as these compounds affect the effectiveness of the treatment methods used. Milli-Q water should a higher decrease of the bacterial inactivation rate compared to Leman Lake water as a result of the absence of inorganic ions. Even though there is a high difference in salt concentration Leman Lake water and seawater but Inactivation rates were similar to each other. [8] The advanced oxidation processes (AOPs) are presented as treatment of future in disinfection and removal of contaminants from water. [9] Advanced oxidation processes represent a group of techniques used for the treatment of water characterized by the generation of radicals, such as the hydroxyl radical (OHº) and may be an alternative to chlorine disinfection. [10] A Study of Hydrogen Peroxide electro-generation in seawater was done and the result showed that in the absence of a reducing substrate, the fast production rate of active chlorine leads to total depletion of H2O2. And the simultaneous anodic production of oxidizing species, mainly active chlorine, severely affects the stability of hydrogen peroxide due to the chemical reaction between these species. [11] It was found that in order to improve the elimination efficiency an oxidant could be added during UV irradiation which absorbs the UV light by itself and reacts with water to form a highly reactive OH radicals. Hydrogen peroxide (H2O2) and ozone are the commonly used oxidants. It was absorbed during the experiments that the absorbance efficiency of H2O2 is reliant on its concentration. The higher the concentration of H2O2, the better the performance of the water treatment system. [12] It was observed that the oxidation rate of nanomolar Fe(II) with H2O2 is a function of pH, temperature and the concentration of HCO3 - and H2O2. And FeOH+ is the most important iron species controlling the Fe(II) oxidation with H2O2 in the pH range of natural seawater systems. [13] As shown in fig (1), using a concentrated light system that reflects the solar light onto the photocatalytic reactor by a reflecting surface is more desired because it will require a smaller reactor volume, it operates at a higher flow rate, better mass transfer rates, and it can be even operated under cloudy conditions. [14-15]
  • 3. Investigation on the Effect… 52 Figure 1: a parabolic shaped light reflecting II. MATERIALS & METHODS Thin Film Method a- Material Seawater was collected 1 km from Al Athibah Beach, Oman. Aeroxide P25 was obtained from Evonik Industries, 35% Hydrogen Peroxide from The Merck Group, and PVA from Oman Textile Mills Company L.L.C. b- Preparation of Coating Solutions Coating Solution: 5 grams of PVA and 2.2 grams of TiO2 were dissolved in 60ml of water, 30ml of ethanol, 6ml of acetic acid and 4ml of ethylene glycol. The solution was left for stirring overnight. c- Coating of Glass Tube Glass tube is coated with TiO2 thin film by passing the dispersed TiO2 in the inner surface of the tube. The tube is allowed to dry and then calcinated at 400°C for about 1 hour. Fig 2 represents the reactor system configuration. Seawater from the system tank was pumped to the thin film coated reactor using peristaltic pump, where the photo catalysis is activated by sunlight and oxidation reaction takes place. Figure 2: Schematic of the Thin Film Experimental Set-up The tubular photo reactor is 1 meter long with an outer diameter of 2 cm. The system glass tank holds 1.5 litter of seawater water which is continuously re-circulated through the tubular reactor. Suspension Method Fig 3 represents the reactor system configuration. The seawater along with photo catalyst was fed to the reactor system using peristaltic pump, where the photocatalysis is activated by sunlight. Oxidation reaction takes places which lowers poisonousness inorganic matter in the contaminated seawater. Figure 3: Schematic of the Suspension Experimental Set-up
  • 4. Investigation on the Effect… 53 Two tubular photo reactors were connected with a silicon tube. Each tube is 1 meter long with an outer diameter of 2 cm. The system glass tank holds 2 litter of seawater water along with 3 gram of the photo catalyst which is mixed by a magnetic stirrer. The solution is then continuously re-circulated through the tubular reactor. III. RESULT AND DISCUSSION Inorganic Carbon was measured with Total Organic Carbon Analyzer (TOC-L series) from Shimadzu Corporation. a- Thin Film Method Polyvinyl alcohol was used as a solution thickener and a binder to enhance the chemical bonding of TiO2 to the inner surface of the glass tube. The transparent coated layers of TiO2 was stable, very resistance and strongly stick on the inner surface of the tube after calcination. The glass tubes were first illuminated under solar irradiation for 1 hour before it is fitted to the experimental setup. Then the photocatalytic reaction took place at a UV Index of 6 to 8. Table (2) shows seawater analysis with coated tubular photoreactor with TiO2. A slight decrease was noticed in the inorganic carbon value with time. And fig (4) shows the variation in inorganic carbon during photocatalytic reaction of TiO2 with seawater. TABLE (2): Seawater analysis with coated tubular photoreactor. Time 0hr 1hr 2hr 3hr 4hr UV Index - 6 6 8 8 Temperature ºC - 31 32 34 32 IC (ppm) 25.83 25.65 25.26 25.15 25.05 Figure (4): Variation in In-Organic Carbon during photocatalytic reaction of TiO2 with seawater Table (3) shows seawater analysis with coated tubular photoreactor with TiO2 alone with H2O2. The decrease in inorganic carbon value is more when combining TiO2 with H2O2 compared to TiO2 coating alone. Fig (5) shows the variation in inorganic carbon during photocatalytic reaction of TiO2 along with H2O2. TABLE (3): Seawater analysis of coated tubular photoreactor with H2O2. Time 0hr 1hr 2hr 3hr 4hr UV Index - 7 8 8 6 Temperature ºC - 27 29 29 28 IC (ppm) 25.83 24.24 23.33 21.93 21.66
  • 5. Investigation on the Effect… 54 Figure (5): Variation in In-Organic Carbon during photocatalytic reaction of TiO2 and H2O2 with seawater b- Suspension Method The reaction was carried out for 5 hours continuously and a sample of the treated water was collected every 60 min. The samples were not filtered but it was allowed to settle down overnight water analysis is done Table (4) shows seawater analysis with suspended photocatalysis of TiO2. It is observed that the decrease in inorganic carbon value is much more is suspension method compared to thin film method. And fig (6) shows the variation in inorganic carbon during photocatalytic reaction of TiO2 in suspension. TABLE (4): Seawater analysis with suspended photocatalysis. Time 0hr 1hr 2hr 3hr 4hr 5hr UV Index - 5 6 7 6 5 Temperature ºC - 23 23 23 23 23 IC (ppm) 26.2 23.02 22.5 22.14 22.14 21.43 Figure (6): Variation in In-Organic Carbon during photocatalytic reaction of TiO2 in suspension with seawater Table (5) shows seawater analysis with suspended photocatalysis of TiO2. It is spotted that there is a significant decrease in inorganic carbon value of seawater with time. Fig (7) shows the variation in inorganic carbon during photocatalytic reaction of TiO2 in suspension. TABLE (5): Seawater analysis of suspended photocatalysis with H2O2. Time 0hr 1hr 2hr 3hr 4hr 5hr UV Index - 4 5 6 7 6 Temperature ºC - 22 24 25 24 24 IC (ppm) 26.2 21.18 20.98 20.74 18.66 1.084
  • 6. Investigation on the Effect… 55 Figure (7): Variation in In-Organic Carbon during photocatalytic reaction of TiO2 and H2O2 in suspension with seawater IV. CONCLUSION Oman is having high sunlight intensity which makes the utilization of solar photocatalysis an environmentally and sustainable process. Experimental investigations were carried out in an immobilized thin film Nano photo catalyst as well as suspension mode. The degradation of inorganic compounds present in seawater was studied. The following conclusions were drawn:  Nano TiO2 photo catalyst thin film inside the glass tube remains stable with a strong resistance.  Reduction of Inorganic carbon present in seawater after photocatalytic reaction with TiO2.  Reduction of IC was slightly more in the presence of hydrogen peroxide.  A significate reduction of IC was obtained in suspension method with the addition of hydrogen peroxide. V. ACKNOWLEDGMENT The authors would like to acknowledge the financial support received from The Research Council, Oman through grant number 83 (ORG/EI/12/003). The authors also wish to thank Ms. Shamsa Al Saadi for her support in the laboratory and Mr. Salim for his help in fabricating the experimental set-up in CCE’s Workshop and finally Mr. Adil Azjoon from SQU Glass Glowing Workshop for sizing of glass tubes. REFERENCE [1]. Oman Power and Water Procurement Company (OPWP) 7-Year Statement (2014-2020). [2]. Z. Meng, and Z. Juan, “Wastewater Treatment by Photocatalytic Oxidization of Nano-ZnO”, Global Environmental Policy, Japan, No.12, p. 1-9, April, 2008. [3]. Sarmad Ismail, “Disinfection of wastewater using TiO2 semiconductor photochemistry”, Tampere University of Applied Sciences, 2013. [4]. Radwan A.Al Rasheed, Water Treatment by Heterogeneous Photocatalysis an Overview, Saline Water Desalination Research Institute and Saline Water Conversion Corporation (SWCC), Saudi Arabia. [5]. N. B. Mok, “Photocatalytic Degradation of oily Wastewater: Effect of Catalyst Concentration Load, Irradiation Time and Temperature”, BSc thesis, Faculty of Chemical & Natural Resources Engineering, University Malaysia Pahang, 2009. [6]. Bahnemann, D., Bockelmann, D. & Goslich, R. Mechanistic “Studies of water detoxification in illuminated TiO2 suspensions”, Sol. Energy Mater., 1991, 24, 564–583. [7]. Melchor Gonzalez-Davila, J. Magdalena Santana-Casian, and Frank J. Millero, “Oxidation of iron (II) nanomolar with H2O2 in seawater”, Rosenstiel School of Marine and Atmospheric Science, University of Miami,, Geochimica et Cosmochimica Acta, Vol. 69, No. 1, pp. 83-93, 2005. [8]. D. Rubio a ,b, E. Nebot b, J.F. Casanueva c, C. Pulgarin a, “Comparative effect of simulated solar light, UV, UV/H2O2 and photo- Fenton treatment (UV-Vis/ H2O2 /Fe2+ , 3+ ) in the Escherichia coli inactivation in artificial seawater”, Water Research 47 (2013) 6367 6379. [9]. Holm, E.R., Stamper, D.M., Brizzolara, R.A., Barnes, L., Deamer, N.N., Burkholder, J.A., “Sonication of bacteria, phytoplankton and zooplankton: application to treatment of ballast water”, Marine Pollution Bulletin 56, 1201-1208. [10]. De la Cruz, N., Gimenez, J., Esplugas, S., Grandjean, D., de Alencastro, L.F.,Pulgarin,C., :Degradation of 32 emergent contaminants by UV and neutral photo-Fenton in domestic wastewater effluent previously treated by activated sludge” Water Research 46, 1947 1957. [11]. Elisabetta Petrucci, Daniele Montanaro, Luca Di Palma, “A Feasibility Study of Hydrogen Peroxide Electrogeneration in Seawater for Environmental Remediation”, The Italian Association of Chemical Engineering. ISBN 978-88-95608-19-8; ISSN 1974-9791. [12]. Muriel Sona, Christine Baus, Heinz-Jürgen Brauch, “UV Irradiation versus combined UV / Hydrogen Peroxide and UV / Ozone Treatment for the Removal of Persistent Organic Pollutants from Water”, International Conference Ozone and UV, April 3rd 2006. [13]. Melchor Gonzalez-Davila, J. Magdalena Santana-Casian, and Frank J. Millero, “Oxidation of iron (II) nanomolar with H2O2 in seawater”, Rosenstiel School of Marine and Atmospheric Science, University of Miami,, Geochimica et Cosmochimica Acta, Vol. 69, No. 1, pp. 83-93, 2005. [14]. R. Thiruvenkatachari, S. Vigneswaran, Il Shik Moon, “A Review on UV/TiO2 Photocatalytic Oxidation Process”, Korean j. chem. eng., 25(1), 64-72 2008, vol. 25, p. 64-72, 2008. [15]. New Technology Demonstration Program, Parabolic-Trough Solar Water Heating. [Online] available: http://smartenergy.arch.uiuc.edu/pdf/Archive/ParabolicTroughSOlarWaterHeater.pdf