scholarly journals UV/Tio2 photocatalytic reactor for real textile wastewaters treatment

2014 ◽  
Vol 70 (10) ◽  
pp. 1670-1676 ◽  
Author(s):  
Maurício da Motta ◽  
Raquel Pereira ◽  
M. Madalena Alves ◽  
Luciana Pereira

Textile dye wastewaters are characterized by strong colour, salts and other additives, high pH, temperature, chemical oxygen demand (COD) and biodegradable materials. Being aesthetically and environmentally unacceptable, these wastewaters need to be treated before their discharge. Anaerobic bioprocesses have been proposed as being environmentally friendly and relatively cheap; however, when applied to real effluent with a complex composition, they can fail. In this study, a photoreactor combining UV light and TiO2, immobilized in cellulosic fabric, was applied for the treatment of two industrial textile wastewaters. High colour and COD removal, and detoxification, were achieved for both wastewaters, at controlled pH of 5.5. Effluents showed very poor biodegradability due to their complex composition; thus, the proposed process is an efficient alternative.

2017 ◽  
Vol 16 (9) ◽  
pp. 1881-1889 ◽  
Author(s):  
Rui A.R. Boaventura ◽  
Carmen S.D. Rodrigues ◽  
Luis M. Madeira

Proceedings ◽  
2019 ◽  
Vol 16 (1) ◽  
pp. 44
Author(s):  
Kozak ◽  
Włodarczyk-Makuła

The aim of the research was to determine the effectiveness of removing micro-organic pollutants, including PAHs, using the modified Fenton method. The tested material was pretreated coke wastewater, in which the initial chemical oxygen demand (COD) value and initial polycyclic aromatic hydrocarbons (PAHs) concentration were determined. The samples were then subjected to an oxidation procedure. Before the process, the pH was adjusted to 3.5–3.8. Next, the following doses of sodium carbonate—hydrogen peroxide (2/3): 1.2 g/L, 1.5 g/L and 2 g/L, and a constant dose of iron sulphate were added. The next step was exposing the samples to UV light for 6 min and separating the organic matrix from the samples of wastewater. After the tests, the final value of the COD and the final PAHs concentration were determined. The average content of organic pollutants in pretreated coke wastewater determined by the COD index was 538 mg/L, and after the oxidation process, the COD index decreased in the range from 9 to 29%. The efficiency of the degradation of the sum of 16 PAHs was varied and was in the range of 94–97.6%. The research results show that sodium carbonate—hydrogen peroxide (2/3) can be used for the degradation of organic pollutants, such as PAHs, in the modified Fenton process.


1999 ◽  
Vol 40 (1) ◽  
pp. 183-190 ◽  
Author(s):  
N. H. Ince ◽  
G. Tezcanlı

Treatability of textile dye-bath effluents by advanced oxidation with Fenton and Fenton-like reagents (FeII/H2O2 and FeIII/H2O2), in the presence and absence of UV light was investigated, using a reactive azo-dye (Procion Red HE7B), and typical dye bath constituents. Under the experimental conditions employed, it was found that with 20 min UV irradiation, complete color removal and 79% total organic carbon degradation is possible, when the system is operated at pH=3, and with a H2O2/Fe(II) molar ratio of 20:1. The increased dissolved solids content of the treated solution implies the necessity of an appropriate membrane system to make the effluent reusable in the dye/wash processes.


2011 ◽  
Vol 11 (3) ◽  
pp. 253-257 ◽  
Author(s):  
Winarti Andayani ◽  
Agustin N M Bagyo

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.


Author(s):  
Weerana Eh Kan ◽  
Jamil Roslan ◽  
Ruzinah Isha

<p>Conservative desalination technology including distillation requires high energy and cost to operate. Hence, pretreatment process can be done prior to desalination to overcome energy demand and cost reduction. Objective of this research is to study the effect of calcination temperature of hybrid catalyst in photocatalytic reactor system in the seawater desalination, i.e. salt removal in the seawater. The catalyst was synthesized via wet impregnation method with 1:1 weight ratio of TiO<sub>2</sub> and activated oil palm fiber ash (Ti:Ash). The catalyst was calcined at different temperature, i.e. 500 <sup>o</sup>C and 800 <sup>o</sup>C. The study was carried out in a one liter Borosilicate photoreactor equipped with mercury light of 365 nanometers for two hours with 400 rpm mixing and catalyst to seawater sample weight ratio of 1:400. The Chemical Oxygen Demand (COD), pH, dissolved oxygen (DO), turbidity and conductivity of the seawater were analyzed prior and after the testing. The fresh and spent catalysts were characterized via X-Ray Diffractogram (XRD and Nitrogen physisorption analysis. The calcination temperature significantly influenced the adsorption behaviour and photocatalytic activity. However, Ti:Ash which calcined at 800 <sup>o</sup>C has less photocatalytic activity. It might be because the surface of fiber ash was sintered after calcined at high temperature. The Ti:Ash catalyst that calcined at 500 <sup>o</sup>C was found to be the most effective catalyst in the desalination of seawater by reducing the salt concentration of more than 9 % compared to Ti:Ash calcined at 800 <sup>o</sup>C. It can be concluded that catalyst calcination at 500 °C has better character, performance and economically feasible catalyst for seawater desalination. Copyright © 2016 BCREC GROUP. All rights reserved</p><p><em>Received: 22<sup>nd</sup> January 2016; Revised: 23<sup>rd</sup> February 2016; Accepted: 23<sup>rd</sup> February 2016</em></p><strong>How to Cite:</strong> Kan, W.E., Roslan, J., Isha R. (2016). Effect of Calcination Temperature on Performance of Photocatalytic Reactor System for Seawater Pretreatment. <em>Bulletin of Chemical Reaction Engineering &amp; Catalysis</em>, 11 (2): 230-237 (doi:10.9767/bcrec.11.2.554.230-237)<p><strong>Permalink/DOI:</strong> http://dx.doi.org/10.9767/bcrec.11.2.554.230-237</p>


2019 ◽  
Vol 8 (1) ◽  
pp. 895-900 ◽  
Author(s):  
Santhanam Mohan ◽  
Manickam Vishnu Devan

Abstract The photocatalysis of Ag/Ni bi-metallic nano-particles on safranin O dye degradation was evaluated by UV light irradiations. Ag/Ni bi-metallic nanoparticles were synthesized by the green approach using Zingiber officinale root (Zinger) extract. The average particles size of Ag/Ni bi-metallic nanoparticles was found to be 70-88 nm from SEM image and from XRD patterns it was confirmed that the existence of Ag/Ni bi-metallic nano-particles. 8 mg of Ag/Ni bi-metallic nanoparticles present in 40 mL of 10 ppm dye, degraded completely in presence of UV light irradiations within 30 min time durations. The effect of dye degradation within a short period of time (30 min) was due to wide band gap energy and photochemical redox reactions.


2020 ◽  
Vol 69 (4) ◽  
pp. 345-354 ◽  
Author(s):  
Sakthisharmila Palanisamy ◽  
Palanisamy Nachimuthu ◽  
Mukesh Kumar Awasthi ◽  
Balasubramani Ravindran ◽  
Soon Woong Chang ◽  
...  

Abstract Textile effluents contain triazine-substituted reactive dyes that cause health problems such as cancer, birth defects, and hormone damage. An electrochemical process was employed effectively to degrade azo reactive dye with the aim of reducing the production of carcinogenic chemicals during biodegradation. Textile dye C.I. Reactive Red 2 (RR2), a model pollutant that contains dichloro triazine ring, was subjected to the electrocoagulation process using aluminium (Al) electrodes. A maximum of 97% of colour and 72% of chemical oxygen demand (COD) removal efficiencies were achieved and 9.5 kWh/kg dye electrical energy and 0.8 kg Al/kg dye electrode consumption were observed. The dye removal mechanism was studied by analysing the results of UV-Vis spectra of RR2 and treated samples at various time intervals during electrocoagulation. Fourier transform infrared (FTIR) spectra and energy dispersive X-ray (EDX) spectral studies were used for analysing the electrocoagulated flocs. The results indicate that in this process the dye gets removed by adsorption and there is no significant carcinogenic by-product formation during the degradation of dye.


Author(s):  
Mayowa Oladele Agunbiade ◽  
Carolina Pohl ◽  
Esta Van Heerden ◽  
Oluwaseun Oyekola ◽  
Anofi Ashafa

This study evaluated the potential of a biopolymeric flocculant produced by Terrabacter sp. isolated from Sterkfontein Dam, South Africa. Microbial flocculants aid the aggregation of suspended solutes in solutions, thus, suggesting its alternative application to inorganic and synthetic organic flocculants, which are associated with health-related problems. The 16S rDNA analysis revealed the bacteria to have 98% similarity to Terrabacter sp. MUSC78T and the sequence was deposited in the Genbank as Terrabacter sp. with accession number KF682157.1. A series of experimental parameters such as bioflocculant dosage, cations concentrations, pH, and application of the purified bioflocculant in wastewaters treatment were investigated. In the presence of glucose as a sole carbon source, Ca2+ as cation at pH 8, the optimal flocculating activity attained was 85%. Optimum bioflocculant dosage of 0.5 mg/mL was able to remove chemical oxygen demand (COD), biological oxygen demand (BOD), suspended solids (SS), nitrate, and turbidity in dairy wastewater. In addition, the tested bioflocculant exhibited higher flocculating efficiency as compared to polyaluminum chloride, polyethylenime, and alum. Inductible coupled plasma optical emission spectroscopy (ICP-OES) analyses confirmed significant removal of 77.7% Fe, 74.8% Al, 61.9% Mn, and 57.6% Zn as representatives of heavy metals from treated dairy wastewater. Fourier transform infrared spectroscopy (FTIR) indicated the presence of carboxyl, hydroxyl, and amino groups in the purified bioflocculant which could be responsible for flocculation. Findings from this study showed the prospect of the studied bioflocculant as an alternative candidate in wastewater treatment and remediating of heavy metals.


2017 ◽  
Vol 15 (7) ◽  
pp. 491-501
Author(s):  
Sunun KHAMI ◽  
Wipawee KHAMWICHIT ◽  
Ratthapol RANGKUPAN ◽  
Kowit SUWANNAHONG

In this paper, toluene removal via photocatalytic oxidation using TiO2 dip coated nanofilms is presented. Nanofilms were synthesized from bacterial cellulose using the electrospinning technique. The physical properties of the nanofilms were analyzed by scanning electron microscopy (SEM). The ratio of bacterial cellulose/nylon used in the spinning process was 0.165:1. The results from SEM showed that the structure of the TiO2 composite nanofilms was rutile crystalline with an average particle size of 20 nm, and synthesized nanofilms had an average size of 20 - 30 nm. The band gap energies of TiO2-dip coated nanofilms ranged from 3.18 - 3.21 eV. SEM results of TiO2 coated nanofilms suggested that the TiO2 was rather uniformly distributed onto the surface of the nanofilms. The actual amount of TiO2 coated on the nanofilms was estimated using thermogravimetric analysis (TGA) for 1x1 cm2 surface area. It was found that 0.1852, 0.2897 and 0.7275 mg of TiO2 were coated on the surface of the nanofilms for 1, 2.5 and 5 % (weight) TiO2 dosage, respectively. The photocatalytic activity of the nanofilms was tested for the removal of gaseous toluene in a photocatalytic reactor. Experimental conditions were set as follows: UV light intensity of approximately 2.7 mW.cm-2, flow rate of 0.2 L.min-1, and an initial toluene concentration of about 200±20 ppm, and a retention time at 200 min. The degradation rate of toluene increased with increasing dosage of TiO2 from 1, 2.5 and 5 %. The nanofilms at a 5 % dosage yielded the highest removal efficiency of 92.71 %, followed by the 2.5 and 1 % dosage, respectively.


Sign in / Sign up

Export Citation Format

Share Document