Influence of anionic surfactant on the process of electro-Fenton decolorized methyl orange

2010 ◽  
Vol 61 (5) ◽  
pp. 1299-1306
Author(s):  
B. X. Ren
Keyword(s):  
Methyl Orange ◽  
Sodium Dodecyl ◽  
Order Reaction ◽  
Fenton Process ◽  
Methyl Orange Degradation ◽  
First Order ◽  
Pseudo First Order ◽  
Kinetics Of ◽  
Sds Surfactant ◽  
Industry Wastewater

The electro-Fenton process has been shown to be very successful to remove dyes from water. However, the influence of other constituents in dyeing industry wastewater, such as Sodium Dodecyl Sulfate (SDS) surfactants, has not been investigated. In this study, the effect of SDS surfactant on the kinetics of Methyl Orange degradation undergoing Electro-Fenton process was investigated. Results show that Methyl Orange degradation rate decreased as SDS concentration (below Critical Micelle Concentration, CMC) increased, which was attributed to the consumption of hydroxyl radicals (˙OH) by surfactants. The kinetics modeling indicates the reaction was the first-order reaction to Methyl Orange even SDS existing. The pseudo first-order rate constants decreased as SDS concentration increased.

Effect of anionic surfactants on the process of Fenton degradation of methyl orange

2009 ◽  
Vol 60 (11) ◽  
pp. 2803-2807 ◽  
Author(s):  
C. W. Yang ◽  
D. Wang
Keyword(s):  
Methyl Orange ◽  
Anionic Surfactants ◽  
Sodium Dodecyl ◽  
Degradation Pathway ◽  
Fenton Process ◽  
Methyl Orange Degradation ◽  
First Order ◽  
Kinetics Modelling ◽  
Kinetics Of ◽  
Sds Surfactant

Fenton process has been shown to be very successful to remove dyes from water. However, the influence of other constituents in dyeing industry wastewater, such as Sodium Dodecyl Sulphate (SDS) surfactants, has not been investigated. In this study, the effect of SDS surfactant on the kinetics of Methyl Orange degradation undergoing Fenton process was investigated. Results show that Methyl Orange degradation rate decreased as SDS concentration increased, which was attributed to the consumption of hydroxyl radicals (∙OH) by surfactants and the formation of Methyl Orange-SDS complex. No evidence was found that the Methyl Orange degradation pathway was affected by the presence of SDS. The kinetics modelling indicates the reaction was the first-order reaction to Methyl Orange.

Kinetics of Cs adsorption/desorption on granite by a pseudo first order reaction model

2007 ◽  
Vol 275 (3) ◽  
pp. 555-562 ◽  
Author(s):  
Shih-Chin Tsai ◽  
Tsing-Hai Wang ◽  
Yuan-Yaw Wei ◽  
Wen-Chun Yeh ◽  
Yi-Lin Jan ◽  
...  
Keyword(s):  
Reaction Model ◽  
Order Reaction ◽  
First Order Reaction ◽  
Pseudo First Order Reaction ◽  
First Order ◽  
Pseudo First Order ◽  
Adsorption Desorption ◽  
Kinetics Of

Degradation of propoxycarbazone-sodium with advanced oxidation processes

2011 ◽  
Vol 11 (1) ◽  
pp. 129-134 ◽  
Author(s):  
A. Dulov ◽  
N. Dulova ◽  
Y. Veressinina ◽  
M. Trapido
Keyword(s):  
Rate Constants ◽  
Advanced Oxidation Processes ◽  
Advanced Oxidation ◽  
Fenton Process ◽  
Oxidation Processes ◽  
First Order ◽  
Order Rate ◽  
Conversion Time ◽  
Pseudo First Order ◽  
Kinetics Of

The degradation of propoxycarbazone-sodium, an active component of commercial herbicide, in aqueous solution with ozone, UV photolysis and advanced oxidation processes: O3/UV, O3/UV/H2O2, H2O2/UV, and the Fenton process was studied. All these methods of degradation proved feasible. The kinetics of propoxycarbazone-sodium degradation in water followed the pseudo-first order equation for all studied processes except the Fenton treatment. The application of schemes with ozone demonstrated low pseudo-first order rate constants within the range of 10−4 s−1. Addition of UV radiation to the processes improved the removal of propoxycarbazone-sodium and increased the pseudo-first order rate constants to 10−3 s−1. The Fenton process was the most efficient and resulted in 5 and 60 s of half-life and 90% conversion time of propoxycarbazone-sodium, respectively, at 14 mM H2O2 concentration. UV treatment and the Fenton process may be recommended for practical application in decontamination of water or wastewater.

scholarly journals Investigation into the Adsorption of Methylene Blue and Methyl Orange by UiO-66-NO2 Nanoparticles

2021 ◽  
Vol 2021 ◽  
pp. 1-10
Author(s):  
Hien Thi Dinh ◽  
Nam Trung Tran ◽  
Dai Xuan Trinh
Keyword(s):  
Methylene Blue ◽  
Methyl Orange ◽  
Adsorption Capacity ◽  
Metal Organic Framework ◽  
Second Order ◽  
Mesomeric Effect ◽  
First Order ◽  
Pseudo Second Order ◽  
Pseudo First Order ◽  
Kinetics Of

In this work, the adsorptive removal of methylene blue and methyl orange by UiO-66-NO2 nanoparticles was studied. The influence of pH on the adsorption capacity was assessed. The kinetics of the adsorption process were investigated and compared with pseudo-first-order, pseudo-second-order, Elovich, and intraparticle models. The kinetics of the adsorption fits moderately with the pseudo-first-order, but perfectly fits with pseudo-second-order models, and has a very good fit with the Elovich and intraparticle models. The adsorption isotherms were measured and compared with the Langmuir and Freundlich models. The adsorption capacity of methyl orange (MO) on UiO-66-NO2 nanoparticles (142.9 mg/g) was over three times higher than that of methylene blue (MB) on the nanoparticles (41.7 mg/g). The discrepancy between these capacities was attributed to the presence of the -NO2 functional group, which caused a strong negative mesomeric effect in the metal-organic framework structure.

scholarly journals Photocatalytic and Photoelectrocatalytic Degradation of Methyl Orange Using Graphite/PbTiO3 Composite

2018 ◽  
Vol 16 (3) ◽  
pp. 347
Author(s):  
Candra Purnawan ◽  
Sayekti Wahyuningsih ◽  
Pramudita Putri Kusuma
Keyword(s):  
Methyl Orange ◽  
Rate Constant ◽  
Order Reaction ◽  
First Order Reaction ◽  
Methyl Orange Degradation ◽  
First Order ◽  
Photoelectrocatalytic Degradation ◽  
Methyl Orange Concentration ◽  
Degradation Reaction ◽  
Radiation Time

Synthesis of graphite/PbTiO3 composite as a catalyst in photodegradation and photoelectrodegradation process of methyl orange have been conducted. The purposes of this research are to study the effect of radiation time, composition of composite, voltage and pH of solution for methyl orange degradation. Photodegradation process of methyl orange was carried out for 5; 10; 15; 20; 25 and 30 min. Ratio of graphite : PbTiO3 (w/w) were varied at 1:3; 1:2; 1:1; 2:1 and 3:1. Meanwhile, the applied voltages were 7.5; 10 and 12.5 V and the photoelectrodegradation was conducted under pH condition of 3; 7; and 11, respectively. The result showed that optimum composition of graphite/PbTiO3 in the methyl orange photodegradation was obtained at 1:1 ratio for 30 min with degradation up to 90.43% ± 0.062. The degradation reaction follows first order reaction with a rate constant of 0.0688 min-1. The optimum voltage is 10 V, in which it reduced the methyl orange concentration up to 92.65% ± 0 with a rate constant 0.0941 min-1 for first order reaction. The optimum pH is pH = 11, that provide methyl orange reduction up to 95.28% ± 0.082.

Kinetic of oxidation of methyl orange by vanadium(V) under conditions VO2+ and decavanadates coexist: Catalysis by Triton X-100 micellar medium

2019 ◽  
Author(s):  
Chem Int
Keyword(s):  
Methyl Orange ◽  
Solution Ph ◽  
Vanadium Concentration ◽  
Limiting Behavior ◽  
First Order ◽  
First Order Kinetics ◽  
Ph Range ◽  
Kinetic Pattern ◽  
Triton X ◽  
Kinetics Of

The kinetics of oxidation of methyl orange by vanadium(V) {V(V)} has been investigated in the pH range 2.3-3.79. In this pH range V(V) exists both in the form of decavanadates and VO2+. The kinetic results are distinctly different from the results obtained for the same reaction in highly acidic solution (pH < 1) where V(V) exists only in the form of VO2+. The reaction obeys first order kinetics with respect to methyl orange but the rate has very little dependence on total vanadium concentration. The reaction is accelerated by H+ ion but the dependence of rate on [H+] is less than that corresponding to first order dependence. The equilibrium between decavanadates and VO2+ explains the different kinetic pattern observed in this pH range. The reaction is markedly accelerated by Triton X-100 micelles. The rate-[surfactant] profile shows a limiting behavior indicative of a unimolecular pathway in the micellar pseudophase.

The Kinetics of Glucose Decomposition with Sulfate Reduction in the Anaerobic Fluidized Bed Reactor

1993 ◽  
Vol 28 (2) ◽  
pp. 135-144 ◽  
Author(s):  
S. Matsui ◽  
R. Ikemoto Yamamoto ◽  
Y. Tsuchiya ◽  
B. Inanc
Keyword(s):  
Sulfate Reduction ◽  
Fluidized Bed ◽  
Kinetic Equations ◽  
Fluidized Bed Reactor ◽  
Order Reaction ◽  
First Order Reaction ◽  
First Order ◽  
Glucose Decomposition ◽  
Reaction Equations ◽  
Kinetics Of

Using a fluidized bed reactor, experiments on glucose decomposition with and without sulfate reduction were conducted. Glucose in the reactor was mainly decomposed into lactate and ethanol. Lactate was mainly decomposed into propionate and acetate, while ethanol was decomposed into propionate, acetate, and hydrogen. Sulfate reduction was not involved in the decomposition of glucose, lactate, and ethanol, but was related to propionate and acetate decomposition. The stepwise reactions were modeled using either a Monod expression or first order reaction kinetics in respect to the reactions. The coefficients of the kinetic equations were determined experimentally. The modified Monod and first order reaction equations were effective at predicting concentrations of glucose, lactate, ethanol, propionate, acetate, and sulfate along the beight of the reactor. With sulfate reduction, propionate was decomposed into acetate, while without sulfate reduction, accumulation of propionate was observed in the reactor. Sulfate reduction accelerated propionate conversion into acetate by decreasing the hydrogen concentration.

Kinetics and Mechanism of Hexachloroiridate(IV) Oxidation of Arsenic(III) in Acidic Perchlorate Solutions

1992 ◽  
Vol 57 (7) ◽  
pp. 1451-1458 ◽  
Author(s):  
Refat M. Hassan
Keyword(s):  
Ionic Strength ◽  
Fractional Order ◽  
Activation Parameters ◽  
Order Reaction ◽  
First Order Reaction ◽  
Intermediate Complex ◽  
Constant Ionic Strength ◽  
Kinetics Of Oxidation ◽  
First Order ◽  
Kinetics Of

The kinetics of oxidation of arsenic(III) by hexachloroiridate(IV) at lower acid concentrations and at constant ionic strength of 1.0 mol dm-3 have been investigated spectrophotometrically. A first-order reaction in [IrCl62-] and fractional order with respect to arsenic(III) have been observed. A kinetic evidence for the formation of an intermediate complex between the hydrolyzed arsenic(III) species and the oxidant was presented. The results showed that decreasing the [H+] is accompanied by an appreciable acceleration of the rate of oxidation. The activation parameters have been evaluated and a mechanism consistent with the kinetic results was suggested.

Efficient adsorption of chlorpyrifos onto modified activated carbon by gamma irradiation; a plausible adsorption mechanism

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Mohamed S. Yahia ◽  
Ahmed S. Elzaref ◽  
Magdy B. Awad ◽  
Ahmed M. Tony ◽  
Ahmed S. Elfeky
Keyword(s):  
Gamma Irradiation ◽  
Area Measurement ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
X Ray ◽  
First Order ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Pseudo First Order ◽  
Kinetics Of

Abstract Commercial Granulated Active Carbon (GAC) has been modified using 10 Gy dose Gamma irradiation (GAC10 Gy) for increasing its ability of air purification. Both, the raw and treated samples were applied for removing Chlorpyrifos pesticide (CPF) from ambient midair. Physicochemical properties of the two materials were characterized by Fourier Transform Infrared (FT-IR) and Raman spectroscopy. The phase formation and microstructure were monitored using X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), supported with Energy-Dispersive X-ray (EDX). The Surface area measurement was detected using BET particle size prosometry. Obtained outcomes showed that, the maximum adsorption capacity, given by Langmuir equations, was greatly increased from 172.712 to 272.480 mg/g for GAC and GAC10 Gy, respectively, with high selectivity. The overall removal efficiency of GAC10 Gy was notably comparable to that of the original GAC-sorbent. The present study indicated that, gamma irradiation could be a promising technique for treating GAC and turned it more active in eliminating the pesticides pollutants from surrounding air. The data of equilibrium has been analyzed by Langmuir and Freundlich models, that were considerably better suited for the investigated materials than other models. The process kinetics of CPF adsorbed onto both tested carbon versions were found to obey the pseudo first order at all concentrations with an exception at 70 mg/l using GAC, where, the spontaneous exothermic adsorption of Chlorpyrifos is a strong function for the pseudo-first order (PFO) and pseudo second order (PSO) kinetics.

Multifactorial optimization of the decolorisation parameters of wastewaters resulting from dyeing flowers

2009 ◽  
Vol 59 (7) ◽  
pp. 1361-1369 ◽  
Author(s):  
Edison Gil Pavas ◽  
Miguel Ángel Gómez-García
Keyword(s):  
Hydrogen Peroxide ◽  
Organic Matter ◽  
Experimental Design ◽  
Order Reaction ◽  
Pseudo First Order Reaction ◽  
First Order ◽  
Effluent Standards ◽  
Degradation Of Dyes ◽  
Pseudo First Order ◽  
Dyes Mixture

This work deals with the treatment of the wastewaters resulting from the process of dyeing flowers. In some local cases for growing flowers near to Medellín (Colombia), wastewater color was found to be one of the main problems in meeting local effluent standards. Wastewaters were treated by photodegradation process (which includes photocatalysis) to achieve the degradation of dyes mixture and organic matter in the wastewater. A multifactorial experimental design was proposed, including as experimental factors the following variables: pH, and the concentration of both catalyst (TiO2) and hydrogen peroxide (H2O2). According to the obtained results, at the optimized variables values, it is possible to reach a 99% reduction of dyes, a 76.9% of mineralization (TOC) and a final biodegradability of 0.834. Kinetic analysis allows proposing a pseudo first order reaction for the reduction, the mineralization, and the biodegradation processes.

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