scholarly journals Molecular Basis of the Mechanism of Thiol Oxidation by Hydrogen Peroxide in Aqueous Solution: Challenging the SN2 Paradigm

2012 ◽  
Vol 25 (3) ◽  
pp. 741-746 ◽  
Author(s):  
Ari Zeida ◽  
Ryan Babbush ◽  
Mariano C. González Lebrero ◽  
Madia Trujillo ◽  
Rafael Radi ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Hydrogen Peroxide ◽  
Molecular Basis ◽  
Thiol Oxidation ◽  
Oxidation By Hydrogen Peroxide

Kinetics of sulphur(IV) oxidation by hydrogen peroxide in basic aqueous solution

1996 ◽  
Vol 30 (7) ◽  
pp. 1013-1018 ◽  
Author(s):  
J. Lagrange ◽  
C. Pallares ◽  
G. Wenger ◽  
P. Lagrange
Keyword(s):  
Aqueous Solution ◽  
Hydrogen Peroxide ◽  
Kinetics Of ◽  
Oxidation By Hydrogen Peroxide

Kinetic Studies on Sb(III) Oxidation by Hydrogen Peroxide in Aqueous Solution

2004 ◽  
Vol 38 (10) ◽  
pp. 2843-2848 ◽  
Author(s):  
François Quentel ◽  
Montserrat Filella ◽  
Catherine Elleouet ◽  
Christian-Louis Madec
Keyword(s):  
Aqueous Solution ◽  
Hydrogen Peroxide ◽  
Kinetic Studies ◽  
Oxidation By Hydrogen Peroxide

Reactions in Activated Peroxide Systems and their Influences on Bleaching Performance

2020 ◽  
Vol 17 ◽  
Author(s):  
Xiaoyan Wang ◽  
Jinmei Du ◽  
Changhai Xu
Keyword(s):  
Aqueous Solution ◽  
Hydrogen Peroxide ◽  
Energy Efficiency ◽  
Textile Industry ◽  
High Energy ◽  
Side Reactions ◽  
Competitive Reactions ◽  
High Energy Efficiency ◽  
Hydrolysis Of ◽  
Bleach Activators

Abstract:: Activated peroxide systems are formed by adding so-called bleach activators to aqueous solution of hydrogen peroxide, developed in the seventies of the last century for use in domestic laundry for their high energy efficiency and introduced at the beginning of the 21st century to the textile industry as an approach toward overcoming the extensive energy consumption in bleaching. In activated peroxide systems, bleach activators undergo perhydrolysis to generate more kinetically active peracids that enable bleaching under milder conditions while hydrolysis of bleach activators and decomposition of peracids may occur as side reactions to weaken the bleaching efficiency. This mini-review aims to summarize these competitive reactions in activated peroxide systems and their influence on bleaching performance.

Heterogeneous Fenton Catalytic Removal of Organic Pollutant in Aqueous Solution by using Coal Gangue as a Catalyst

2019 ◽  
Vol 12 (4) ◽  
pp. 312-325
Author(s):  
Jiwei Zhang ◽  
Jingjing Xu ◽  
Shuaixia Liu ◽  
Baoxiang Gu ◽  
Feng Chen ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Hydrogen Peroxide ◽  
Hydroxyl Radical ◽  
Removal Rate ◽  
Organic Pollutant ◽  
Coal Gangue ◽  
Ion Leakage ◽  
Heterogeneous Fenton ◽  
Solution Ph ◽  
X Ray

Background: Coal gangue was used as a catalyst in heterogeneous Fenton process for the degradation of azo dye and phenol. The influencing factors, such as solution pH gangue concentration and hydrogen peroxide dosage were investigated, and the reaction mechanism between coal gangue and hydrogen peroxide was also discussed. Methods: Experimental results showed that coal gangue has the ability to activate hydrogen peroxide to degrade environmental pollutants in aqueous solution. Under optimal conditions, after 60 minutes of treatment, more than 90.57% of reactive red dye was removed, and the removal efficiency of Chemical Oxygen Demand (COD) up to 72.83%. Results: Both hydroxyl radical and superoxide radical anion participated in the degradation of organic pollutant but hydroxyl radical predominated. Stability tests for coal gangue were also carried out via the continuous degradation experiment and ion leakage analysis. After five times continuous degradation, dye removal rate decreased slightly and the leached Fe was still at very low level (2.24-3.02 mg L-1). The results of Scanning Electron Microscope (SEM), energy dispersive X-Ray Spectrometer (EDS) and X-Ray Powder Diffraction (XRD) indicated that coal gangue catalyst is stable after five times continuous reuse. Conclusion: The progress in this research suggested that coal gangue is a potential nature catalyst for the efficient degradation of organic pollutant in water and wastewater via the Fenton reaction.

Decomposition of hydrogen peroxide on a two-component NiO-CdO catalyst and the effect of ionizing radiation on its catalytic properties

1979 ◽  
Vol 44 (4) ◽  
pp. 1015-1022 ◽  
Author(s):  
Viliam Múčka
Keyword(s):  
Aqueous Solution ◽  
Hydrogen Peroxide ◽  
Catalytic Activity ◽  
Nickel Oxide ◽  
Catalytic Properties ◽  
Cadmium Oxide ◽  
Chemisorb Oxygen ◽  
Composition Region ◽  
Chemisorbed Oxygen ◽  
Two Component

The catalytic properties of two-component catalyst nickel oxide-cadmium oxide with the proportions of the components covering the whole composition region 0-100% were examined by studying the decomposition of hydrogen peroxide in aqueous solution on it. In the range 0-25 mol.% CdO, cadmium oxide is found to affect infavourably the ability of nickel oxide to chemisorb oxygen. The amount of the chemisorbed oxygen increases several times on gamma irradiation of the samples. The effect of cadmium oxide on the catalytic activity of the system shows up in fresh samples only indirectly via the changed amount of the oxygen chemisorbed. In older samples the initial catalytic activity of the system is changed, which can be explained based on the concept of bivalent catalytic centres in terms of the co-action of the catalytic centres of the two oxides, which are in equilibrium. The irradiation of the system under study speeds up the processes leading to the establishing of this equilibrium which is thermally very stable, and results in a substantial increase of the catalytic activity of the samples investigated.

Oxidation of ethylenediphosphinetetraacetate anions

1983 ◽  
Vol 48 (9) ◽  
pp. 2604-2608
Author(s):  
Jana Podlahová ◽  
Jaroslav Podlaha
Keyword(s):  
Aqueous Solution ◽  
Hydrogen Peroxide ◽  
Electronic Structure ◽  
Acid Solutions ◽  
Tetraacetic Acid ◽  
Single Product ◽  
Weakly Acid ◽  
Inhibiting Effect ◽  
Oxidation By Molecular Oxygen ◽  
Protonated Forms

The oxidation of the ethylenediphosphinetetraacetate anion and its protonated forms by iodine, periodate, hydrogen peroxide, and oxygen has been studied in aqueous solution. The oxidation by the first three reagents is fast and yields a single product, bis(phosphine oxide), which has been isolated and characterized as ethylenebis(phosphinyl)tetraacetic acid. The oxidation by molecular oxygen proceeds considerably more slowly; in weakly acid solutions its rate is determined by the properties of the oxygen rather than by the electronic structure of the various protonated substrate species. The inhibiting effect of the phosphonium structures takes place only in strongly acid solutions.

Enzymatic colorimetry of lecithin and sphingomyelin in aqueous solution.

1983 ◽  
Vol 29 (8) ◽  
pp. 1513-1517 ◽  
Author(s):  
M W McGowan ◽  
J D Artiss ◽  
B Zak
Keyword(s):  
Aqueous Solution ◽  
Hydrogen Peroxide ◽  
Amniotic Fluid ◽  
Enzymatic Reaction ◽  
Detergent Solution ◽  
Enzymatic Determination ◽  
Red Color ◽  
Hydrolysis Of ◽  
Zwitterionic Detergent

Abstract A procedure for the enzymatic determination of lecithin and sphingomyelin in aqueous solution is described. The phospholipids are first dissolved in chloroform:methanol (2:1 by vol), the solvent is evaporated, and the residue is redissolved in an aqueous zwitterionic detergent solution. The enzymatic reaction sequences of both assays involve hydrolysis of the phospholipids to produce choline, which is then oxidized to betaine, thus generating hydrogen peroxide. The hydrogen peroxide is subsequently utilized in the enzymatic coupling of 4-aminoantipyrine and sodium 2-hydroxy-3,5-dichlorobenzenesulfonate, an intensely red color being formed. The presence of a non-reacting phospholipid enhances the hydrolysis of the reacting phospholipid. Thus we added lecithin to the sphingomyelin standards and sphingomyelin to the lecithin standards. This precise procedure may be applicable to determination of lecithin and sphingomyelin in amniotic fluid.

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