ChemInform Abstract: STUDIES OF OXIDATIONS BY FENTON′S REAGENT USING REDOX TITRATION PART 4, OXIDATION OF ETHANOL AND T-BUTYL ALCOHOL

1973 ◽  
Vol 4 (30) ◽  
pp. no-no
Author(s):  
D. L. INGLES
Keyword(s):  
Butyl Alcohol ◽  
Redox Titration ◽  
Oxidation Of Ethanol

Studies of oxidations by fenton's reagent using redox titrations. IV. Oxidation of ethanol and t-butyl alcohol

1973 ◽  
Vol 26 (5) ◽  
pp. 1015 ◽  
Author(s):  
DL Ingles
Keyword(s):  
Reaction Rates ◽  
Butyl Alcohol ◽  
Oxidation Products ◽  
Fenton’S Reagent ◽  
Copper Salts ◽  
Redox Titration ◽  
Fenton's Reagent ◽  
Titration Procedure ◽  
Free Hydroxyl ◽  
Oxidation Of Ethanol

The oxidation of ethanol by Fenton's reagent was studied to confirm the validity of the redox titration procedure. A quantitative analysis of oxidation products during the complete oxidation of ethanol and its consecutive oxidation products is presented. � The oxidation of t-butyl alcohol was studied under a number of different conditions and yields of acetone and the dimer, 2,5- dimethylhexane-2,5-diol, were obtained. The effects of oxygen, copper salts, and chloride and bromide ions on this oxidation were studied. ��� The ratio of reaction rates of ethanol and t-butyl alcohol with the free hydroxyl radical was determined.

Studies of oxidations by fenton's reagent using redox titration. V. Effect of complex formation on reaction mechanism

1973 ◽  
Vol 26 (5) ◽  
pp. 1021 ◽  
Author(s):  
DL Ingles
Keyword(s):  
Reaction Mechanism ◽  
Complex Formation ◽  
Hydroxyl Radical ◽  
Butyl Alcohol ◽  
Fenton’S Reagent ◽  
Redox Titration ◽  
Fenton's Reagent ◽  
Free Hydroxyl ◽  
Electron Transfers ◽  
H2o2 System

The effect of complex formation on the oxidation of substrate in the Fe2+-H2O2 system has been studied. t-Butyl alcohol which is normally oxidized to the dimer, 2,5-dimethylhexane-2,5-diol, by Fenton's reagent has been used as a probe for the presence of free hydroxyl radical. ��� It is shown that when suitable complexes are formed substrates are not oxidized by free hydroxyl radical. Instead, new mechanisms involving one- and two-electron transfers within a substrate-ferrous ion-peroxide complex are proposed.

Isothermal and isobaric vapour-liquid equilibrium data in the tetrachloromethane-sec-butyl alcohol system

1983 ◽  
Vol 48 (9) ◽  
pp. 2446-2453 ◽  
Author(s):  
Jan Linek
Keyword(s):  
Experimental Data ◽  
Boiling Point ◽  
Butyl Alcohol ◽  
Correlation Equations ◽  
Wilson Equation ◽  
Liquid Equilibrium ◽  
Raoult’S Law ◽  
System A ◽  
Equilibrium Data ◽  
Alcohol System

Isothermal vapour-liquid equilibrium data at 65, 73 and 80 °C and isobaric ones at 101.3 kPa were measured in the tetrachloromethane-sec-butyl alcohol system. A modified circulation still of the Gillespie type was used for the measurements. Under the conditions of measurement, the system exhibits positive deviations from Raoult's law and minimum boiling-point azeotropes. The experimental data were fitted to a number of correlation equations, the most suitable being the Wilson equation.

Thermodynamic and Kinetic Investigation of the Solvent Effect on the Oxidation of [Co(en)2SCH2COO]+ with S2O82- In Water-Methanol and Water-tert-Butyl Alcohol Mixtures

1993 ◽  
Vol 58 (5) ◽  
pp. 1001-1006 ◽  
Author(s):  
Oľga Vollárová ◽  
Ján Benko
Keyword(s):  
Transfer Functions ◽  
Activation Parameters ◽  
Butyl Alcohol ◽  
Oxidation Of Co ◽  
Kinetics Of Oxidation ◽  
Tert Butyl ◽  
Tert Butyl Alcohol ◽  
Alcohol Mixtures ◽  
Kinetics Of

The kinetics of oxidation of [Co(en)2SCH2COO]+ with S2O82- was studied in water-methanol and water-tert-butyl alcohol mixtures. Changes in the reaction activation parameters ∆H≠ and ∆S≠ with varying concentration of the co-solvent depend on the kind of the latter, which points to a significant role of salvation effects. The solvation effect on the reaction is discussed based on a comparison of the transfer functions ∆Ht0, ∆St0 and ∆Gt0 for the initial and transition states with the changes in the activation parameters accompanying changes in the CO-solvent concentration. The transfer enthalpies of the reactant were obtained from calorimetric measurements.

Solubility and Thermodynamic Transfer Functions of Cesium Dianilinetetraisothiocyanatochromate(III)

1998 ◽  
Vol 63 (3) ◽  
pp. 293-298
Author(s):  
Vladislav Holba
Keyword(s):  
Experimental Data ◽  
Isopropyl Alcohol ◽  
Transfer Functions ◽  
Butyl Alcohol ◽  
Aqueous Methanol ◽  
Gibbs Energies ◽  
Gibbs Energy Of Transfer ◽  
Energy Of Transfer ◽  
The Given ◽  
Reference Electrolyte

The solubilities of cesium dianilinetetraisothiocyanatochromate(III) in water as well as in aqueous methanol, isopropyl alcohol, tert-butyl alcohol and acetonitrile were measured as a function of temperature and solvent composition. The Gibbs energies, enthalpies and entropies of transfer of the salt from water to the given solvents have been evaluated from experimental data. The contribution of [Cr(C6H5NH2)2(NCS)4]- ion to the Gibbs energy of transfer of the investigated salt has been calculated using the tetraphenylarsonium tetraphenylborate (TATB) reference electrolyte assumption.

Oxidation of Ethanol on Sn-Mo Oxide Catalysts

1992 ◽  
Vol 57 (3) ◽  
pp. 439-445
Author(s):  
Magdy A. Wassel ◽  
Nalla K. Allahaverdova ◽  
Tofki G. Alkhazov
Keyword(s):  
Acetic Acid ◽  
Potassium Hydroxide ◽  
Pulse Method ◽  
Conversion Ratio ◽  
Mo Catalyst ◽  
Acid Ratio ◽  
Aqueous Potassium Hydroxide ◽  
The Stability ◽  
Primary Oxidation ◽  
Oxidation Of Ethanol

To determine the acidic and basic properties of the title catalysts, the adsorption of NH3 and SO2 was compared using pulse method. It was found that this characteristics undergoes changes when the Sn-Mo catalyst is treated with aqueous potassium hydroxide solutions of different concentrations. The catalyst treated with the more concentrated KOH solution possesses mainly properties of a base. When studying the oxidation of ethanol it has been found that the αCO2/αaldehyde conversion ratio increases with the time of contact of the mixture with the catalyst while the αCO2/α acid ratio is not affected. The study of two alcohols deuterated either in OH group (C2H5OD) or in the alkyl group ((C2D5OH) has shown that the substitution of C-H for C-D bond enhances the stability of the primary oxidation product, deuterated ethanal, so that it is not transformed further to acetic acid.

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