Oxidative Degradation of Organic Pollutants by Hydrogen Peroxide in the Presence of FePz(dtnCl2)4under Visible Irradiation

2007 ◽  
Vol 36 (5) ◽  
pp. 586-587 ◽  
Author(s):  
Jie Sun ◽  
Yuping Sun ◽  
Kejian Deng ◽  
Haobo Hou ◽  
Duoyuan Wang
Keyword(s):  
Hydrogen Peroxide ◽  
Organic Pollutants ◽  
Oxidative Degradation ◽  
Visible Irradiation

The Research on RhodamineB Degradation in MW/H2O2 System under Alkaline Environment

2011 ◽  
Vol 105-107 ◽  
pp. 1505-1508 ◽  
Author(s):  
Nan Nan Yuan ◽  
Jun Hong
Keyword(s):  
Hydrogen Peroxide ◽  
Oxidative Degradation ◽  
Order Kinetic ◽  
Optimum Conditions ◽  
Alkaline Environment ◽  
Photodegradation Efficiency ◽  
Initial Ph ◽  
Visible Irradiation ◽  
Single Factor Experiment ◽  
Better Than

In this work, the degradation of Rhodamine B by hydrogen peroxide under microwave irradiation is studied and the optimum conditions are designed by single factor experiment. The UV-VIS spectral changes of RhB solution is detected under the optimum conditions. The results indicate that microwave induction can efficiently improve the oxidative degradation of RhB by hydrogen peroxide in alkaline solution, espcially the dye has the best photodegradation efficiency more than 99% when the concentration of RhB was 300mg/l and the pH of solution was 12 after irradiated for 10min, It is better than RhB under visible irradiation in alkaline environment with hydrogen peroxide. The solution initial pH has no effect on the temporal absorption spectral of RhB. The process of reaction conforms to the first-order kinetic equation.

scholarly journals The Use of Sodium Carbonate—Hydrogen Peroxide (2/3) in the Modified Fenton Reaction to Degradation PAHs in Coke Wastewater

Proceedings ◽  
2019 ◽  
Vol 16 (1) ◽  
pp. 44
Author(s):  
Kozak ◽  
Włodarczyk-Makuła
Keyword(s):  
Hydrogen Peroxide ◽  
Organic Pollutants ◽  
Sodium Carbonate ◽  
Uv Light ◽  
Oxygen Demand ◽  
Organic Matrix ◽  
Coke Wastewater ◽  
Polycyclic Aromatic ◽  
Pahs Concentration ◽  
Modified Fenton

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.

A review of lignin hydrogen peroxide oxidation chemistry with emphasis on aromatic aldehydes and acids

Holzforschung ◽  
2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Ajinkya More ◽  
Thomas Elder ◽  
Zhihua Jiang
Keyword(s):  
Hydrogen Peroxide ◽  
Oxidative Degradation ◽  
Reaction Medium ◽  
Dicarboxylic Acids ◽  
Aromatic Aldehydes ◽  
Product Distribution ◽  
Reaction Conditions ◽  
Alkaline Conditions ◽  
The Stability ◽  
Oxidation Chemistry

Abstract This review discusses the main factors that govern the oxidation processes of lignins into aromatic aldehydes and acids using hydrogen peroxide. Aromatic aldehydes and acids are produced in the oxidative degradation of lignin whereas mono and dicarboxylic acids are the main products. The stability of hydrogen peroxide under the reaction conditions is an important factor that needs to be addressed for selectively improving the yield of aromatic aldehydes. Hydrogen peroxide in the presence of heavy metal ions readily decomposes, leading to minor degradation of lignin. This degradation results in quinones which are highly reactive towards peroxide. Under these reaction conditions, the pH of the reaction medium defines the reaction mechanism and the product distribution. Under acidic conditions, hydrogen peroxide reacts electrophilically with electron rich aromatic and olefinic structures at comparatively higher temperatures. In contrast, under alkaline conditions it reacts nucleophilically with electron deficient carbonyl and conjugated carbonyl structures in lignin. The reaction pattern in the oxidation of lignin usually involves cleavage of the aromatic ring, the aliphatic side chain or other linkages which will be discussed in this review.

Oxidative Degradation of Toxic Organic Pollutants by Water Soluble Nonheme Iron(IV)-Oxo Complexes of Polydentate Nitrogen Donor Ligands

2021 ◽  
Author(s):  
Sandip Munshi ◽  
Rahul Dev Jana ◽  
Tapan Kanti Paine
Keyword(s):  
Organic Pollutants ◽  
Oxidative Degradation ◽  
Heme Iron ◽  
Water Soluble ◽  
Donor Ligands ◽  
Nitrogen Donor Ligands ◽  
Polydentate Ligands ◽  
Oxo Complexes ◽  
Non Heme Iron ◽  
Nitrogen Donor

The ability of four mononuclear non-heme iron(IV)-oxo complexes supported by nitrogen donor polydentate ligands in degrading organic pollutants has been investigated. The water soluble iron(II) complexes upon treatment with ceric...

Simultaneous photochemical generation of ozone in the gas phase and photolysis of aqueous reaction systems using one VUV light source

1997 ◽  
Vol 35 (4) ◽  
pp. 41-48 ◽  
Author(s):  
T.M. Hashem ◽  
M. Zirlewagen ◽  
A. M. Braun
Keyword(s):  
Gas Phase ◽  
Light Source ◽  
Organic Pollutants ◽  
Vacuum Ultraviolet ◽  
Oxidative Degradation ◽  
Reaction System ◽  
Photochemical Reactions ◽  
Experimental Conditions ◽  
Photochemical Generation ◽  
Kinetics Of

A more efficient use of vacuum ultraviolet (VUV) radiation produced by an immersed Xe-excimer light source (172 nm) was investigated for the oxidative degradation of organic pollutants in aqueous systems. All emitted VUV radiation from one light source was used in two simultaneous but separate photochemical reactions: (1) photochemical generation of ozone by irradiating oxygen in the gas phase and (2) photolysis of the aqueous reaction system. The gas stream containing the generated ozone is sparged into the reaction system, thus enhancing the oxidative degradation of organic pollutants. The photochemically generated ozone in the gas phase was quantitatively analyzed, and the kinetics of the degradation of 4-chlorophenol (4-CP) and of the dissolved organic carbon (DOC) were determined under different experimental conditions. The results show that the rates of degradation of the substrate and of the DOC decrease in the order of the applied processes, VUV/O3 > O3 > VUV.

Combinative dyebath treatment with activated carbon and UV/H2O2: a case study on Everzol Black-GSP®

2002 ◽  
Vol 46 (4-5) ◽  
pp. 51-58 ◽  
Author(s):  
N.H. Ince ◽  
D.A. Hasan ◽  
B. Üstün ◽  
G. Tezcanli
Keyword(s):  
Hydrogen Peroxide ◽  
Activated Carbon ◽  
Carbon Mineralization ◽  
Oxidative Degradation ◽  
Advanced Oxidation ◽  
Color Removal ◽  
Operating Parameters ◽  
Cost Reductions ◽  
H2o2 System

Treatability of textile dyebath effluents by two simultaneously operated processes comprising adsorption and advanced oxidation was investigated using a reactive dyestuff, Everzol Black-GSP® (EBG). The method was comprised of contacting aqueous solutions of the dye with hydrogen peroxide and granules of activated carbon (GAC) during irradiation of the reactor with ultraviolet light (UV). Control experiments were run separately with each individual process (advanced oxidation with UV/H2O2 and adsorption on GAC) to select the operating parameters on the basis of maximum color removal. The effectiveness of the combined scheme was tested by monitoring the rate of decolorization and the degree of carbon mineralization in effluent samples. It was found that in a combined medium of advanced oxidation and adsorption, color was principally removed by oxidative degradation, while adsorption contributed to the longer process of dye mineralization. Economic evaluation of the system based on total color removal and 50% mineralization showed that in the case of Everzol Black-GSP®, which adsorbs relatively poorly on GAC, the proposed combination provides 25% and 35% reduction in hydrogen peroxide and energy consumption relative to the UV/H2O2 system. Higher cost reductions are expected in cases with well adsorbing dyes and/or with less costly adsorbents.

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