Dataset Information

Use of an Environmental Pollutant From Hexavalent Chromium Removal as a Green Catalyst in The Fenton Process.

ABSTRACT: The present study refers to the use of an environmental pollutant generated during the removal of hexavalent chromium from aqueous media. This pollutant is a material with catalytic properties suitable for application in the oxidative degradation of problematic organic compounds. The material, initially used as an adsorbent, is a composite prepared by modifying the crystalline phases of iron oxides together with the chitosan (CT-FeCr). Chemical and morphological characterizations of the materials were performed using SEM analysis coupled with EDS, XRD and DSC. The CT-FeCr beads were used in the degradation of methylene blue dye (MB) and showed excellent degradation potential (93.6%). The presence of Cr on the surface of the catalyst was responsible for the increase in catalytic activity compared to the CT-Fe and pure magnetite materials. The product of the effluent treatment and the presence of the catalyst itself in the environment do not pose toxic effects. In addition, the CT-FeCr beads showed catalytic stability for several consecutive reaction cycles with possible technical and economic viability. The concept of "industrial symbiosis" may be applied to this technology, with that term relating to the reuse of a byproduct generated in one particular industrial sector by another as a raw material.

SUBMITTER: Chagas PMB

PROVIDER: S-EPMC6731299 | biostudies-literature | 2019 Sep

REPOSITORIES: biostudies-literature

ACCESS DATA

Publications

Use of an Environmental Pollutant From Hexavalent Chromium Removal as a Green Catalyst in The Fenton Process.

Chagas Pricila Maria Batista PMB Caetano Aline Aparecida AA Tireli Aline Auxiliadora AA Cesar Pedro Henrique Souza PHS Corrêa Angelita Duarte AD Guimarães Iara do Rosário IDR

Scientific reports 20190906 1

The present study refers to the use of an environmental pollutant generated during the removal of hexavalent chromium from aqueous media. This pollutant is a material with catalytic properties suitable for application in the oxidative degradation of problematic organic compounds. The material, initially used as an adsorbent, is a composite prepared by modifying the crystalline phases of iron oxides together with the chitosan (CT-FeCr). Chemical and morphological characterizations of the material ...[more]

PMID: 31492935

Similar Datasets

Project description:Chromium contamination is a serious environmental issue in areas affected by leather tanning and metal plating, and green rust sulfate has been tested extensively as a potential material for in situ chemical reduction of hexavalent chromium in groundwater. Reported products and mechanisms for the reaction have varied, most likely because of green rust's layered structure, as reduction at outer and interlayer surfaces might produce different reaction products with variable stabilities. Based on studies of Cr(III) oxidation by biogenic Mn (IV) oxides, Cr mobility in oxic soils is controlled by the solubility of the Cr(III)-bearing phase. Therefore, careful engineering of green rust properties, i.e., crystal/particle size, morphology, structure, and electron availability, is essential for its optimization as a remediation reagent. In the present study, pure green rust sulfate and green rust sulfate with Al, Mg and Zn substitutions were synthesized and reacted with identical chromate (CrO42-) solutions. The reaction products were characterized by X-ray diffraction, pair distribution function analysis, X-ray absorption spectroscopy and transmission electron microscopy and treated with synthetic ?-MnO2 to assess how easily Cr(III) in the products could be oxidized. It was found that Mg substitution had the most beneficial effect on Cr lability in the product. Less than 2.5% of the Cr(III) present in the reacted Mg-GR was reoxidized by ?-MnO2 within 14 days, and the particle structure and Cr speciation observed during X-ray scattering and absorption analyses of this product suggested that Cr(VI) was reduced in its interlayer. Reduction in the interlayer lead to the linkage of newly-formed Cr(III) to hydroxyl groups in the adjacent octahedral layers, which resulted in increased structural coherency between these layers, distinctive rim domains, sequestration of Cr(III) in insoluble Fe oxide bonding environments resistant to reoxidation and partial transformation to Cr(III)-substituted feroxyhyte. Based on the results of this study of hexavalent chromium reduction by green rust sulfate and other studies, further improvements can also be made to this remediation technique by reacting chromate with a large excess of green rust sulfate, which provides excess Fe(II) that can catalyze transformation to more crystalline iron oxides, and synthesis of the reactant under alkaline conditions, which has been shown to favor chromium reduction in the interlayer of Fe(II)-bearing phyllosilicates.

Dataset Information

Use of an Environmental Pollutant From Hexavalent Chromium Removal as a Green Catalyst in The Fenton Process.

Publications

Use of an Environmental Pollutant From Hexavalent Chromium Removal as a Green Catalyst in The Fenton Process.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets