Rate of reaction of dithionite ion with oxygen in aqueous solution

1964 ◽  
Vol 19 (3) ◽  
pp. 522-525 ◽  
Author(s):  
J. A. Morello ◽  
Margot R. Craw ◽  
H. P. Constantine ◽  
R. E. Forster
Keyword(s):  
Aqueous Solution ◽  
Reaction Rate ◽  
Initial Rate ◽  
Sodium Dithionite ◽  
Zero Order ◽  
Flowing Liquid ◽  
First Order ◽  
Rate Of Reaction ◽  
Dithionite Ion ◽  
Kinetics Of

The rate of removal of oxygen from aqueous solution by sodium dithionite in 0.1 m sodium hydroxide was studied in a rapid-reaction apparatus using a membrane-covered polarographic cell to determine Po2 in the flowing liquid. The measurements were made at 37 C, so that the data would be applicable in studies of the kinetics of oxyhemoglobin in blood. The initial concentrations in the mixed reacting solution were between 8 x 10-5 m and 47.5 x 10-5 m for dithionite, and either 10 x 10-5 m or 47.8 x 10-5 m for O2. The reaction over the first 40 msec was found to be first order with respect to dithionite and zero order with respect to molecular oxygen. The initial rate constant was 42.5 ± sd 3.6 sec-1. oxygen reduction by dithionite; hemoglobin; deoxygenation rate; dithionite-oxygen reaction rate Submitted on June 17, 1963

The mechanism of the oxidation of thiocyanate ion by peroxomonosulphate in aqueous solution. II. Kinetics of the reaction

1966 ◽  
Vol 19 (8) ◽  
pp. 1365 ◽  
Author(s):  
RH Smith ◽  
IR Wilson
Keyword(s):  
Aqueous Solution ◽  
Initial Rate ◽  
Stopped Flow ◽  
Thiocyanate Ion ◽  
First Order ◽  
Conductance Method ◽  
Rate Of Reaction ◽  
Kinetics Of

Initial rates of reaction for the above oxidation have been measured by a stopped-flow conductance method. Between pH 2 and 3.6, the initial rate of reaction, R, is given by the expression R{[HSO5-]+[SCN-]} = {kb+kc[H+]}[HSO5-]0[SCN-]20+ka[H+]-1[HSO5]20[SCN-]0 As pH increases, there is a transition to a pH-independent rate, first order in each thiocyanate and peroxomonosulphate concentrations.

Mechanism of Hg(II) Oxidation of D-Galactose in Alkaline Medium

1978 ◽  
Vol 33 (6) ◽  
pp. 657-659 ◽  
Author(s):  
M. P. Singh ◽  
A. K. Singh ◽  
Mandhir Kumar
Keyword(s):  
Alkaline Medium ◽  
Reaction Rate ◽  
Reducing Sugar ◽  
Zero Order ◽  
Ion Concentration ◽  
Kinetics Of Oxidation ◽  
Ion Concentrations ◽  
First Order ◽  
Kinetics Of ◽  
Direct Proportionality

Abstract The present paper deals with the kinetics of oxidation of D-galactose by Nessler's reagent in alkaline medium. The reaction is zero order with respect to Hg(II) and first order with respect to reducing sugar. The direct proportionality of the reaction rate at low hydroxide ion concentrations shows retarding trend at higher concentrations. The reaction rate is inversely proportional to iodide ion concentration. A mechanism has been proposed taking HgI3- as the reacting species

scholarly journals Photoinitiated Polymerization of 2-Hydroxyethyl Methacrylate by Riboflavin/Triethanolamine in Aqueous Solution: A Kinetic Study

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Iqbal Ahmad ◽  
Kefi Iqbal ◽  
Muhammad Ali Sheraz ◽  
Sofia Ahmed ◽  
Tania Mirza ◽  
...  
Keyword(s):  
Initial Rate ◽  
Hydroxyl Group ◽  
Hydroxyethyl Methacrylate ◽  
First Order ◽  
First Order Kinetics ◽  
Rate Of Polymerization ◽  
Rate Of Reaction ◽  
Ph Range ◽  
Kinetics Of ◽  
Increased Activity

The polymerization of 1–3 M 2-hydroxyethyl methacrylate (HEMA) initiated by riboflavin/triethanolamine system has been studied in the pH range 6.0–9.0. An approximate measure of the kinetics of the reaction during the initial stages (~5% HEMA conversion) has been made to avoid the effect of any variations in the volume of the medium. The concentration of HEMA in polymerized solutions has been determined by a UV spectrophotometric method at 208 nm with a precision of ±3%. The initial rate of polymerization of HEMA follows apparent first-order kinetics and the rates increase with pH. This may be due to the presence of a labile proton on the hydroxyl group of HEMA. The second-order rate constants for the interaction of triethanolamine and HEMA lie in the range of 2.36 to  M−1 s−1 at pH 6.0–9.0 suggesting an increased activity with pH. An increase in the viscosity of HEMA solutions from 1 M to 3 M leads to a decrease in the rate of polymerization probably as a result of the decrease in the reactivity of the flavin triplet state. The effect of pH and viscosity of the medium on the rate of reaction has been evaluated.

Hydrogenation of Fatty Acid Esters. II. Kinetics of Hydrogenation of Methyl (Z)- and (E)-9-Octadecenoate Catalyzed by a Ziegler Nickel Catalyst

1992 ◽  
Vol 57 (12) ◽  
pp. 2583-2592 ◽  
Author(s):  
Jana Krupičková ◽  
Jaroslav Včelák ◽  
Jiří Hetflejš
Keyword(s):  
Fatty Acid ◽  
Nickel Catalyst ◽  
Fractional Order ◽  
Initial Rate ◽  
Zero Order ◽  
Model Catalyst ◽  
Fatty Acid Esters ◽  
First Order ◽  
Kinetics Of ◽  
Acid Esters

Kinetics of the title reactions has been studied, using nickel(II) 2,4-pentanedionate/triethylaluminium system as a model catalyst. Initial rate measurements showed that in both cases the hydrogenation is first order in hydrogen, zero order in the octadecanoate and a fractional order (close to one) in the catalyst. Both hydrogenations have similar activation energies (30.2 ± 2.3 kJ mol-1 and 28.9 ± 2.6 kJ mol-1 for the (Z)- and (E)-9-octadecenoate, respectively). Based on these data and the results of competition experiments, two models have been proposed to describe isomerization of the octadecenoates (either direct or via an intermediate).

scholarly journals Kinetics and Mechanism of Oxidation of Malic Acid by N-Bromonicotinamide (NBN) in the Presence of a Micellar System

2015 ◽  
Vol 52 ◽  
pp. 111-119
Author(s):  
L. Pushpalatha
Keyword(s):  
Malic Acid ◽  
Reaction Rate ◽  
Activation Parameters ◽  
Zero Order ◽  
Micellar System ◽  
First Order ◽  
First Order Kinetics ◽  
Rate Of Reaction ◽  
Different Temperatures ◽  
Experimental Findings

The oxidation of malic acid by N-bromonicotinamide in the presence of micellar system is studied. First order kinetics with respect to NBN is observed. The kinetics results indicate that the first order kinetics in hydroxy acid at lower concentrations tends towards a zero order at its higher concentrations. Inverse fractional order in [H+] and [nicotinamide] are noted throughout its tenfold variation. Variation of [Hg (OAc)2] and ionic strength of the medium do not bring about any significant change in the rate of reaction. Rate of the reaction increases with a decrease in the percentage of acetic acid. Decrease in the rate constant was observed with the increase in [SDS]. The values of rate constants observed at four different temperatures were utilized to calculate the activation parameters. A suitable mechanism consistent with the experimental findings has been proposed.

Kinetics and Mechanism of the Homogeneous Oxidation of Quinaldine Red by Hydrogen Peroxide

2001 ◽  
Vol 215 (5) ◽  
Author(s):  
Ibrahim A. Salem ◽  
M. El-Maazawi
Keyword(s):  
Aqueous Solution ◽  
Hydrogen Peroxide ◽  
Kinetics And Mechanism ◽  
Cationic Dye ◽  
First Order ◽  
Homogeneous Oxidation ◽  
Rate Of Reaction ◽  
Kinetics Of ◽  
Quinaldine Red

The kinetics of the oxidation of quinaldine red, a cationic dye, using hydrogen peroxide has been studied in aqueous solution. The rate of reaction was found to be first order in [quinaldine red] whereas in hydrogen peroxide it varies from one to zero with increasing [H

Kinetics of the Reaction for Generation of Chlorine Dioxide from Sodium Chlorate and Hydrochloric Acid

2013 ◽  
Vol 634-638 ◽  
pp. 546-550
Author(s):  
Xin Jie Li ◽  
Dan Dan Jiang ◽  
Yue Jun Zhang
Keyword(s):  
Hydrochloric Acid ◽  
Chlorine Dioxide ◽  
Reaction Rate ◽  
Initial Rate ◽  
Reaction System ◽  
Sodium Chlorate ◽  
Second Order ◽  
First Order ◽  
Mixed Order ◽  
Kinetics Of

Based on the mechanism of ClO3-/Cl-reaction system, the kinetics for reaction of sodium chlorate and hydrochloric acid to generate ClO2was studied. The rate equation of this reaction system was deduced and simplified as a formula with mixed-order (combination of first-order and second-order) towards ClO3-. This rate formula indicates that the initial rate of the reaction is the first-order with respect to ClO3-, and the reaction rate is the second-order with respect to ClO3-when [ClO3-] becomes close to zero. The rate constants of the first-order were determined as 0.0168s-1(30°C), 0.0221s-1(40°C), and 0.0279s-1(50°C), respectively, and that of the second-order were obtained for 0.0019L·mol-1·s-1(30°C), 0.0028L·mol-1·s-1(40°C), and 0.0060L·mol-1·s-1(50°C), respectively. The results of statistic test prove that the rate formula obtained in this work is credible.

Effect of crystallographic orientation on the kinetics of reaction of aluminium single crystal in aqueous solution of sodium hydroxide

1987 ◽  
Vol 52 (1) ◽  
pp. 88-92 ◽  
Author(s):  
Milica Miadoková ◽  
Magdalena Plchová ◽  
Ivan Halaša
Keyword(s):  
Activation Energy ◽  
Aqueous Solution ◽  
Apparent Activation Energy ◽  
Sodium Hydroxide ◽  
Crystallographic Orientation ◽  
Reaction Rate ◽  
Rate Of Reaction ◽  
Crystallographic Planes ◽  
Kinetics Of Reaction ◽  
Kinetics Of

The effect of the concentration of OH- ions, oxygen pressure, and temperature on the rate of reaction of aluminium in aqueous solution of sodium hydroxide was studied for surface planes corresponding to the (100), (110), and (111) crystallographic planes. Kinetic anisotropy was observed: the reaction rate increased and the apparent activation energy decreased in order (100)-(110)-(111). The kinetic parameters were related to some physical characteristics of the surface.

Kinetics of catalytic reduction of nitrogen oxide by carbon monoxide on CuO/Al2O3 catalyst

1983 ◽  
Vol 48 (11) ◽  
pp. 3202-3208 ◽  
Author(s):  
Zdeněk Musil ◽  
Vladimír Pour
Keyword(s):  
Carbon Monoxide ◽  
Nitrogen Oxide ◽  
Rate Equation ◽  
Catalytic Reduction ◽  
Zero Order ◽  
Spectroscopic Measurements ◽  
First Order ◽  
Ir Spectroscopic ◽  
Kinetics Of ◽  
Al2o3 Catalyst

The kinetics of the reduction of nitrogen oxide by carbon monoxide on CuO/Al2O3 catalyst (8.36 mass % CuO) were determined at temperatures between 413 and 473 K. The reaction was found to be first order in NO and zero order in CO. The observed kinetics are consistent with a rate equation derived from a mechanism proposed on the basis of IR spectroscopic measurements.

The kinetics of the decarboxylation of β-resorcylic acid in catechol

1976 ◽  
Vol 29 (2) ◽  
pp. 443 ◽  
Author(s):  
MA Haleem ◽  
MA Hakeem
Keyword(s):  
Rate Equation ◽  
Kinetic Data ◽  
Reaction Rate ◽  
Complex Mechanism ◽  
First Order ◽  
Absolute Reaction Rate ◽  
First Time ◽  
Kinetics Of ◽  
Absolute Reaction ◽  
Reaction Rate Equation

Kinetic data are reported for the decarboxylation of β-resorcylic acid in resorcinol and catechol for the first time. The reaction is first order. The observation supports the view that the decomposition proceeds through an intermediate complex mechanism. The parameters of the absolute reaction rate equation are calculated.

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