scholarly journals TiO2 BEADS FOR PHOTOCATALYTIC DEGRADATION OF HUMIC ACID IN PEAT WATER

2011 ◽  
Vol 11 (3) ◽  
pp. 253-257 ◽  
Author(s):  
Winarti Andayani ◽  
Agustin N M Bagyo
Keyword(s):  
Aqueous Solution ◽  
Humic Acid ◽  
Oxalic Acid ◽  
Chemical Oxygen Demand ◽  
Photocatalytic Degradation ◽  
Uv Light ◽  
Batch Reactor ◽  
Oxygen Demand ◽  
Color Intensity ◽  
Before And After

Degradation of humic acid in aqueous solution containing TiO2 coated on ceramics beads under irradiation of 254 nm UV light has been conducted in batch reactor. The aim of this experiment was to study photocatalytic degradation of humic acid in peat water. The irradiation of the humic acid in aqueous solution was conducted in various conditions i.e solely uv, in the presence of TiO2-slurry and TiO2 beads. The color intensity, humic acid residue, conductivity and COD (chemical oxygen demand) of the solution were analyzed before and after irradiation.  The compounds produced during photodegradation were identified using HPLC. The results showed that after photocatalytic degradation, the color intensity and the COD value of the solution decreased, while the conductivity of water increased indicating mineralization of the peat water occurred. In addition, oxalic acid as the product of degradation was observed.

Optimization of Process Parameters for the Photocatalytic Degradation of 2,4-Dichlorophenol in Aqueous Solutions

2009 ◽  
Vol 7 (1) ◽  
Author(s):  
Sushil Kumar Kansal ◽  
Manohar Singh ◽  
Dhiraj Sud
Keyword(s):  
Response Surface Methodology ◽  
Photocatalytic Degradation ◽  
Sodium Hypochlorite ◽  
Uv Light ◽  
Batch Reactor ◽  
Oxygen Demand ◽  
Operational Parameters ◽  
Optimization Of Process Parameters ◽  
Oxidant Concentration ◽  
Optimal Values

In the present study, the photocatalytic degradation of 2,4-DCP has been investigated in a batch reactor under UV light in slurry mode using titania P-25 (surface area 50 m2/g) as a photocatalyst and sodium hypochlorite as an oxidant. Variables studied include catalyst dose, pH and oxidant concentration. The rate of degradation was studied in terms of changes in concentration of the pollutant and reduction in chemical oxygen demand. The optimal values of operational parameters leading to 2,4-DCP abatement were obtained by using response surface methodology.

ZnO Photocatalysis Using Solar Energy for the Removal of Trace Amounts of Alfa-Methylstyrene, Diquat and Indigo Carmine from Water

2014 ◽  
Vol 17 (2) ◽  
Author(s):  
O. M. Shibin ◽  
B. Rajeev ◽  
V. Veena ◽  
E. P. Yesodharan ◽  
Yesodharan Suguna
Keyword(s):  
Visible Light ◽  
Chemical Oxygen Demand ◽  
Photocatalytic Degradation ◽  
Uv Light ◽  
Indigo Carmine ◽  
Parent Compound ◽  
Oxygen Demand ◽  
Solar Photocatalyst ◽  
Significant Chemical ◽  
Trace Pollutants

AbstractSemiconductor photocatalysis using ZnO has been extensively investigated for the chemical and bacterial decontamination of water and air. In most of these cases, UV light is the source of energy and visible light induced photocatalytic degradation of trace pollutants in water has not received adequate attention. In the present study, ZnO is evaluated as a solar photocatalyst for the removal of trace amounts of three typical pollutants, i.e. alpha- Methylstyrene (AMS, a petrochemical), Diquat (herbicide) and Indigo carmine (IC, a dye) from water. Degradation by itself does not result in complete mineralisation and decontamination as seen from the significant Chemical Oxygen Demand even after the parent compound has disappeared. However, the intermediates also get mineralized eventually. The study indicates that solar photocatalysis can be used as a viable tool for the purification water contaminated with these chemicals. The degradation follows variable kinetics depending on the concentration of the substrates. H

Use of Nanopillars-TiO2 Thin Films in the Photocatalytic Degradation of Bromophenol Blue from Aqueous Solution

2018 ◽  
Vol 6 (1) ◽  
pp. 22-30
Author(s):  
C. Lalhriatpuia ◽  
◽  
Thanhming liana ◽  
K. Vanlaldinpuia
Keyword(s):  
Thin Films ◽  
Aqueous Solution ◽  
Photocatalytic Activity ◽  
Photocatalytic Degradation ◽  
Batch Reactor ◽  
Bromophenol Blue ◽  
Tio2 Thin Films ◽  
Initial Concentration ◽  
Bet Specific Surface Area ◽  
Interfering Ions

The photocatalytic activity of Nanopillars-TiO2 thin films was assessed in the degradation of Bromophenol blue (BPB) dye from aqueous solution under batch reactor operations. The thin films were characterized by the XRD, SEM and AFM analytical methods. BET specific surface area and pore sizes were also obtained. The XRD data showed anatase phase of TiO2 particles with average particle size of 25.4 and 21.9 nm, for S1 and S2 catalysts respectively. The SEM and AFM images indicated the catalyst composed with Nanosized pillars of TiO2, evenly distributed on the surface of the substrate. The average height of the pillars was found to be 180 and 40 nm respectively for the S1 and S2 catalyst. The BET specific surface area and pore sizes of S1 and S2 catalyst were found to be 5.217 and 1.420 m2/g and 7.77 and 4.16 nm respectively. The photocatalytic degradation of BPB using the UV light was studied at wide range of physico-chemical parametric studies to determine the mechanism of degradation as well as the practical applicability of the technique. The batch reactor operations were conducted at varied pH (pH 4.0 to 10.0), BPB initial concentration (1.0 to 20.0 mg/L) and presence of several interfering ions, i.e., cadmium nitrate, copper sulfate, zinc chloride, sodium chloride, sodium nitrate, sodium nitrite, glycine, oxalic acid and EDTA in the photocatalytic degradation of BPB. The maximum percent removal of BPB was observed at pH 6.0 and a low initial concentration of the pollutant highly favours the photocatalytic degradation using thin films. The presence of several interfering ions suppressed the photocatalytic activity of thin films to some extent. The time dependence photocatalytic degradation of BPB was demonstrated with the pseudo-first-order rate kinetics. Study was further extended with total organic carbon measurement using the TOC (Total Organic Carbon) analysis. This demonstrated an apparent mineralization of BPB from aqueous solutions.

Degradation of wine distillery wastewaters by the combination of aerobic biological treatment with chemical oxidation by Fenton's reagent

2005 ◽  
Vol 51 (1) ◽  
pp. 167-174 ◽  
Author(s):  
J. Beltran de Heredia ◽  
J. Torregrosa ◽  
J.R. Dominguez ◽  
E. Partido
Keyword(s):  
Chemical Oxygen Demand ◽  
Aromatic Compounds ◽  
Biological Treatment ◽  
Batch Reactor ◽  
Oxygen Demand ◽  
Chemical Oxidation ◽  
Utilization Rate ◽  
Fenton’S Reagent ◽  
Kinetic Rate Constant ◽  
Fenton's Reagent

The degradation of wine distillery wastewaters by aerobic biological treatment has been investigated in a batch reactor. The evolution of the chemical oxygen demand, biomass and total contents of polyphenolic and aromatic compounds was followed through each experiment. According to the Contois model, a kinetic expression for the substrate utilization rate is derived, and its biokinetic constant is evaluated. The final effluents of the aerobic biological experiments were oxidized by Fenton's reagent. The evolution of chemical oxygen demand, hydrogen peroxide concentration and total contents of polyphenolic and aromatic compounds was followed through each experiment. A kinetic model to interpret the experimental data is proposed. The kinetic rate constant of the global reaction is determined.

scholarly journals Synthesis and properties of zeolite/N-doped porous carbon for the efficient removal of chemical oxygen demand and ammonia-nitrogen from aqueous solution

RSC Advances ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 6452-6459 ◽  
Author(s):  
Guangzhi Xin ◽  
Min Wang ◽  
Lin Chen ◽  
Yuzhou Zhang ◽  
Meicheng Wang ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Activated Carbon ◽  
Chemical Oxygen Demand ◽  
Porous Carbon ◽  
Mesoporous Carbon ◽  
Oxygen Demand ◽  
Ammonia Nitrogen ◽  
Efficient Removal ◽  
Porous Activated Carbon

A novel adsorbent zeolite/N-doped porous activated carbon (ZAC) was prepared by the synthesis of zeolite and mesoporous carbon to remove ammonia nitrogen (NH4+–N) and chemical oxygen demand (COD) from aqueous solution.

scholarly journals Photocatalytic Degradation of Polynitrophenols on Various Commercial Suspended or Deposited Titania Catalysts Using Artificial and Solar Light

2008 ◽  
Vol 2008 ◽  
pp. 1-9 ◽  
Author(s):  
Hinda Lachheb ◽  
Ammar Houas ◽  
Jean-Marie Herrmann
Keyword(s):  
Chemical Oxygen Demand ◽  
Photocatalytic Degradation ◽  
Surface Area ◽  
Degradation Rate ◽  
Oxygen Demand ◽  
Solar Light ◽  
Test Reactions ◽  
Anionic Species ◽  
Paper Fibers ◽  
Purification Of Water

Phenol (PH) and three polynitrophenols (4-nitrophenol (PNP), 2,4-dinitrophenol (DNP), 2,4,6-trinitrophenol (TNP)) were photocatalytically degraded by using titania under either artificial or solar light. These four reactions were chosen as test reactions to compare the efficiencies of two suspended commercial titania photocatalysts (Degussa P-25 and Millennium PC-500). It appears that P-25 has a higher initial efficiency in all nitrophenol disappearance reactions. However, for the overall degradation rate, measured by the chemical oxygen demand (COD) disappearance, the performance of PC-500 was similar to that of P25. This was attributed to a favorable textural effect since PC-500 has a much higher surface area which facilitates the readsorption of intermediates. PC-500 was subsequently supported on a special photoinert paper provided by Ahlstrom Company (38-Pont Evèque, France). The influence of the silica binder used for sticking titania particles on the paper fibers was put in evidence as an inhibitor of the coulombic adsorption of anionic species, especially 2,4,6-trinitrophenol, because of the low pzc of silica. Once validated, this supported photocatalyst was introduced in an autonomous solar pilot photoreactor identical to the several prototypes built in the European AQUACAT program. It was demonstrated that the purification of water could be efficiently obtained in a larger scale without any final tedious filtration.

scholarly journals Comparison between the photocatalytic degradation of single and binary azo dyes in TiO2 suspensions under solar light irradiation

2015 ◽  
Vol 5 (4) ◽  
pp. 579-591 ◽  
Author(s):  
Ohm-Mar Min ◽  
Li-Ngee Ho ◽  
Soon-An Ong ◽  
Yee-Shian Wong
Keyword(s):  
Aqueous Solution ◽  
Aqueous Solutions ◽  
Photocatalytic Degradation ◽  
Azo Dyes ◽  
Azo Dye ◽  
Oxygen Demand ◽  
Light Irradiation ◽  
Solar Light ◽  
Acid Orange 7 ◽  
Solar Light Irradiation

Textile industries discharge a large quantity of colored wastewater which is harmful to the ecosystem. In this study, two kinds of dyes were investigated: the mono azo Acid Orange 7 (AO7) and diazo Reactive Green 19 (RG19). The photocatalytic degradation of single (AO7, RG19) azo dye and binary (AO7 and RG19 mixture) azo dye aqueous solutions was photocatalyzed by commercial titanium dioxide (TiO2, P25) under solar light irradiation. The objectives of this study are to compare the photocatalytic degradation between single and binary azo dye aqueous solution and to study the various parameters such as the effect of different initial azo dye concentrations, different initial azo dye pH values, and compare the adsorption capacity of azo dyes with and without solar light irradiation, which influences the photocatalytic activities of single and binary azo dye aqueous solutions in a TiO2 suspension. The results showed that photocatalytic degradation of AO7 and RG19 in a single azo dye aqueous solution was faster than a binary azo dye solution under the solar light irradiation process. Chemical oxygen demand results revealed that complete mineralization could be achieved for both AO7 and RG19 azo dyes under solar light irradiation within 22 hours.

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