Electrochemical Degradation and Degree of Mineralization of the BY28 Dye in a Supporting Electrolyte Mixture Using an Expanded Dimensionally Stable Anode

2021 ◽  
Author(s):  
Raghda M. Belal ◽  
Mohmed A. Zayed ◽  
Rabab M. El-Sherif ◽  
Nabil A. Abdel Ghany
2013 ◽  
Vol 807-809 ◽  
pp. 1362-1367
Author(s):  
Li Li ◽  
Ying Liu ◽  
Yi Fan Li

This study mostly investigated the influences of electrolytic conditions and the structure of electrospinning nanofibers electrodes on the degradation of methylene blue in details. For PAN and Fe/PAN electrodes, was prepared by electrospinning.It was found that the ESF electrodes with higher specific surface area, and higher mesopore percentage could be push the electrochemical degradation. As the same time, adjusted the initial pH, increased the current, and added to electrolyte also could improve the treatment effect of electrochemical degradation. After 90min of electrolysis, the color removal efficiency of methylene blue reached 97.6% at current with 100mA, supporting electrolyte of NaCl with 0.1mol/L and initial pH with 3~5. Under the same current conditions with the Pt-Fe/PAN anodes the color removal rate of degradation were higher efficiency than the other two anodes.


Author(s):  
Sommayeh Saadi ◽  
Parisa Mahmoudpoor Moteshaker ◽  
Seyed Ehsan Rokni ◽  
Ghobad Ahmadidoust ◽  
Narges Farnoodian ◽  
...  

AbstractMetronidazole (MNZ) is one of the pharmaceutical products which is considered as one of the most important pollutants in the environment due to its wide use and resistance to biodegradation. Hence, the purpose of this study is the optimization of the electrochemical degradation of the metronidazole (MNZ) antibiotic using electrochemical oxidation on a stainless steel316 coated with beta lead oxide (SS316/β-PbO2) anode. In the studied electrochemical process, the response surface methodology (RSM) involving a five-level ((pH (A) and electrolysis time (B), current density (C), and MNZ concentration (D)). The central composite design (CCD) was employed for optimizing and modeling of the electrochemical process in the degradation of MNZ. The preparation of SS316/β-PbO2 anode was accomplished using the electro-deposition method. Scanning electron microscope (SEM), energy-dispersive X-ray (EDX), and X-ray diffraction (XRD) analyses were conducted for accurate evaluation and characterization of the coated electrode. The effect of influencing factors on electrochemical degradation of MNZ was studied, and the highest MNZ degradation efficiency was observed to be 98.88% after 120 min under the optimal conditions including the supporting electrolyte concentration of 1.0 g/100 cc, the initial MNZ concentration of 30.1 mg/L, pH of 4 and the current density of 9.99 mA/cm2. The linear regression coefficient (R2) between experiments and different response values in the model was 0.99. Moreover, the statistical analysis of the results indicated that in the range studied, the most effective parameters in MNZ degradation are MNZ concentration and pH. In general, it can be concluded that the electrochemical process using SS316/β-PbO2 anode can effectively eliminate metronidazole, and it can be considered as an efficient method in the degradation of various pollutants.


2010 ◽  
Vol 61 (2) ◽  
pp. 491-498 ◽  
Author(s):  
P. A. Alves ◽  
G. R. P. Malpass ◽  
H. D. Johansen ◽  
E. B. Azevedo ◽  
L. M. Gomes ◽  
...  

In the present study, photo-assisted electrochemical degradation of real textile wastewater was performed. Degradation assays were performed at constant current (40 mA cm−2) in a combined electro/photochemical flow-cell using a Ti/Ru0.3Ti0.7O2 DSA® type electrode. The results show that the method is capable of removing color and chemical oxygen demand (COD) from the effluent. Additionally, the effect of initial pH and type of supporting electrolyte (Na2SO4 or NaCl) was investigated. The principal figures of merit used in this study were COD removal and color removal (605 nm). The results show that up to 72% color and up to 59% COD removal in 120 min is possible under the operating conditions employed. Studies of the phytotoxicity of the wastewater before and after the photo-assisted degradation assays are also presented and the results demonstrate that the toxicity of the effluent is dependent on the length of electrolysis time and the treatment procedure employed.


2011 ◽  
Vol 65 (3) ◽  
Author(s):  
Cornelia Ratiu ◽  
Florica Manea ◽  
Carmen Lazau ◽  
Corina Orha ◽  
Georgeta Burtica ◽  
...  

AbstractThis paper reports the results of an investigation into enhancement of the electrochemical oxidation of p-aminophenol (4-AP) in an aqueous solution with a boron-doped diamond (BDD) electrode, assisted by photocatalysis using a zeolite-supported TiO2 (Z-TiO2) catalyst. The BDD electrode was characterised in 0.1 M Na2SO4-supporting electrolyte and the presence of 4-AP by open-circuit potential behaviour (OCP) and cyclic voltammetry (CV). The electrode behaviour was investigated in the dark and following UV irradiation and in the absence/presence of the Z-TiO2 catalyst. The electro-oxidation process was carried out using chronoamperometry (CA) and multiple-pulsed amperometry (MPA) at the selected potential under potentiostatic conditions. The electrochemical degradation process of 4-AP on the BDD electrode was improved by the application of a pulsed potential, which allowed both in-situ electrochemical cleaning of the electrode and indirect oxidation of 4-AP by oxygen evolution. The application of photocatalysis using Z-TiO2 in the 4-AP electrochemical degradation exhibited an enhanced effect when the anodic potential was set at +1.25 V vs. Ag/AgCl in the water stability region, close to the oxygen evolution potential.


2014 ◽  
Vol 278 ◽  
pp. 221-226 ◽  
Author(s):  
Fernando L. Guzmán-Duque ◽  
Ricardo E. Palma-Goyes ◽  
Ignacio González ◽  
Gustavo Peñuela ◽  
Ricardo A. Torres-Palma

2011 ◽  
Vol 183-185 ◽  
pp. 575-579
Author(s):  
Hui Wang ◽  
Zhao Yong Bian ◽  
Guang Lu ◽  
Xiang Jia Wei ◽  
Xiu Juan Yu ◽  
...  

Electrochemical degradation of phenol was studied in an undivided cell with a Ti/IrO2/RuO2 anode and a carbon/polytetrafluoroethylene (C/PTFE) O2-fed cathode which produced hydrogen peroxide (H2O2) by the electro-reduction of dissolved oxygen. The effect of current density, supporting electrolyte concentration and initial pH on the removal efficiency of phenol were investigated systematically. Results indicated that the optimal removal efficiency of phenol was achieved under the conditions of current density of 39 mA/cm2 and supporting electrolyte concentration of 0.02 mol/L. The phenol removal efficiency in the neutral condition was higher than that of acidic and basic conditions. The chemical oxygen demand (COD) and total organic carbon (TOC) removal achieved 71.6% and 63.6% for 100 min’s electrolysis, respectively. Benzoquinone, maleic acid, oxalic acid, acetic acid and formic acid were identified as intermediates by HPLC. A general phenol degradation pathway involving all these intermediates was proposed.


2011 ◽  
Vol 291-294 ◽  
pp. 1899-1904
Author(s):  
Yong Chun Huang ◽  
Chao Yue Zhao ◽  
Feng Yang ◽  
Ren He

The electrochemical degradation of chitosan was studied with using graphite as anode and cathode, NaCl solution as supporting electrolyte. The effects of current density, temperature, NaCl concentration, pH, chitosan concentration on the degradation dynamics were investigated. It was shown that the electrochemical degradation of chitosan obeys the rule of random degradation, and the kinetic equation was established.


2012 ◽  
Vol 518-523 ◽  
pp. 2505-2508
Author(s):  
Xiao Xing Zhang ◽  
Na Niu ◽  
Ya Qiong Wang ◽  
Wen Lin Xu

The electrochemical degradation of the wastewater of acid blue 41 was studied with Ti/Sb-SnO2 as an anode in which the Sb-SnO2 coating was prepared with a polymeric precursor method. The conversion of acid blue 41 was carried out under galvanostatic control. The effects of current density, initial concentration of acid blue 41 and the concentration of supporting electrolyte on color removal, COD removal and instantaneous current efficiency (ICE) were investigated. The experimental results show that the color removal and COD removal enhance with increasing current density, but ICE decreases. Acid blue 41 can firstly be oxidized by the destroying the conjugated chromophore group and it is difficult that the intermediates produced during the degradation process of cid blue 41 is further degraded.


2020 ◽  
Author(s):  
Tomas Hardwick ◽  
Rossana Cicala ◽  
Nisar Ahmed

<p>Many chiral compounds have become of great interest to the pharmaceutical industry as they possess various biological activities. Concurrently, the concept of “memory of chirality” has been proven as a powerful tool in asymmetric synthesis, while flow chemistry has begun its rise as a new enabling technology to add to the ever increasing arsenal of techniques available to the modern day chemist. Here, we have employed a new simple electrochemical microreactor design to oxidise an L-proline derivative at room temperature in continuous flow. Flow performed in microreactors offers up a number of benefits allowing reactions to be performed in a more convenient and safer manner, and even allow electrochemical reactions to take place without a supporting electrolyte due to a very short interelectrode distance. By the comparison of electrochemical oxidations in batch and flow we have found that continuous flow is able to outperform its batch counterpart, producing a good yield (71%) and a better enantiomeric excess (64%) than batch with a 98% conversion. We have, therefore, provided evidence that continuous flow chemistry has the potential to act as a new enabling technology to replace some aspects of conventional batch processes. </p>


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