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Journal ArticleDOI

p-Nitrophenol degradation by a heterogeneous Fenton-like reaction on nano-magnetite: Process optimization, kinetics, and degradation pathways

Sheng-Peng Sun, +1 more
- 01 Oct 2011 - 
- Vol. 349, Iss: 1, pp 71-79
TLDR
In this paper, a four factor central composite design (CCD) coupled with response surface methodology (RSM) was applied to evaluate and optimize the important variables for the degradation of p-Nitrophenol (p-NP).
Abstract
Heterogeneous Fenton-like reactions on nano-magnetite (Fe 3 O 4 ) were investigated for the degradation of p-Nitrophenol (p-NP). A four factor central composite design (CCD) coupled with response surface methodology (RSM) was applied to evaluate and optimize the important variables. A significant quadratic model ( P -value  R 2  = 0.9442) was derived using analysis of variance (ANOVA), which was adequate to perform the process variables optimization. Optimum conditions were determined to be 1.5 g L −1 Fe 3 O 4 , 620 mM H 2 O 2 , pH 7.0 and 25–45 mg L −1 p-NP. More than 90% of p-NP was experimentally degraded after 10 h of reaction time under the optimum conditions, which agreed well with the model predictions. The results demonstrated that the degradation of p-NP was due to the attack of hydroxyl radicals ( OH) generated by the surface-catalyzed decomposition of hydrogen peroxide on the nano-Fe 3 O 4 , i.e. heterogeneous Fenton-like reactions. Possible mechanisms of p-NP degradation in this system were proposed, based on intermediates identified by LC–MS and GC–MS and included benzoquinone, hydroquinone, 1,2,4-trihydroxybenzene and p-nitrocatechol. The kinetic analysis implied that the generation rate of OH ( V OH ) was increased along with the degradation of p-NP. This was attributed to the formation of acidic products, which decreased the solution pH and enhanced the decomposition of absorbed hydrogen peroxide via a radical producing pathway on the nano-Fe 3 O 4 surface.

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Citations
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Fenton-like degradation of 2,4-dichlorophenol using Fe3O4 magnetic nanoparticles

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Remediation of wastewater using various nano-materials

TL;DR: In this article, the potential developments in nanotechnology with respect to wastewater treatment are reviewed and discussed utilization of various classes of nano-materials for wastewater treatment processes, including activated carbon, carbon nanotubes, grapheme, manganese oxide, zinc oxide, titanium oxide, magnesium oxide and ferric oxides.
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Removal of pharmaceuticals from water by homo/heterogonous Fenton-type processes - A review.

TL;DR: In this review, the impacts of some controlling parameters including the H2O2 and catalyst dosage, solution pH, initial contaminants concentrations, temperature, type of catalyst, intensity of irradiation, reaction time and feeding mode on the removal efficiencies of hetero/homogeneous Fenton processes are discussed.
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Heterogeneous Fenton catalysts for the abatement of organic pollutants from aqueous solution: a review

TL;DR: In this paper, a review of advances in the field of heterogeneous Fenton processes is presented, especially focusing on the various heterogeneous catalysts used in the process and the properties, stability, activity and pollutant degradation mechanism of various catalysts.
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Review on recent developments on pulp and paper mill wastewater treatment

TL;DR: Adopting the integrated methods, alongside a combination of biological and physicochemical treatment methods, can be environmentally and economically preferable to minimize environmental contaminants and energy recycling.
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Magnetic Iron Oxide Nanoparticles: Synthesis, Stabilization, Vectorization, Physicochemical Characterizations, and Biological Applications

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Degradation of organic contaminants in water with sulfate radicals generated by the conjunction of peroxymonosulfate with cobalt.

TL;DR: The advantage of Co/PMS compared to the traditional Fenton Reagent is attributed primarily to the oxidizing strength of the radicals formed, since sulfate radicals are stronger oxidants than hydroxyl and the thermodynamics of the transition-metal-oxidant coupling.
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