Copper Catalyzed Autoxidation of Sulphur Dioxide and Inhibition by Methanoic Acid

2020 ◽  
Vol 10 (1) ◽  
pp. 33-46
Author(s):  
Arun Kumar Sharma ◽  
Devarkonda Satay Narayan Prasad

Background:: Today, acid rain problem is one of the serious global problems to the environment in which pH of the rain water decreases, causing harmful effect to nature, buildings, monuments, vegetation and human being as well. Therefore, the objective of the paper to find out some organic inhibitors present in the atmosphere that inhibited the acid rain. Objective:: In this paper, we studied the chemistry of Cu (II)-methanoic acid-S(IV)-O2 in acetate buffered medium by earlier reported methods in literature. Gravimetric analysis was carried out to find the end product and confirmed that it was sulphate with 98 % recovery. Methods:: Experiments were carried out at 303 ≤ T/K ≤ 313, 4.0 ≤ pH ≤ 5.35, 1.0×10−3 mol/dm3 ≤ S(IV) ≤ 10.0×10−3 mol/dm3, 5×10−6 mol/dm3 ≤ [Cu(II)] ≤ 2.5×10−5 mol/dm3, 6×10−6 mol/dm3≤[methanoic acid]≤7×10-4 mol/dm3. The value of apparent activation energy and inhibition parameter B was calculated in the presence of methanoic acid found as 29.07 kJ mol-1and 3.18 x 103 mol dm-3, respectively. The thermodynamic parameters were found as frequency factor (1.59 x 10-6s-1), entropy (-358.92 J K-1 mol-1), enthalpy (20.97 k J mol-1), and Gibbs free energy (172.83k J mol-1), respectively. Results:: We observed that methanoic acid acts as an inhibitor in copper catalyzed autoxidation of SO2 in acidic medium. Therefore, on the basis of the observed results a free radical mechanism has been identified. The results are useful for modeling rain water acidity and therefore a great use of meteorology and atmospheric chemistry. This study is important in understanding the mechanism of the oxidation of S(IV) by O2. Conclusion:: This study suggests that since organic inhibitors are found in the atmosphere, their concentrations and their influence on the oxidation of aqueous SO2 should be taken into account. The intervention of methanoic acid in the autoxidation of aqueous SO2 plays a role in deciding the fate of both methanoic acid and SO2. The influence of inhibitors may be used to calculate the lifetime of SO2, Methanoic acid has high values of kinh and, therefore, it would be degraded by sulfate radical anions in atmospheric waters.

1963 ◽  
Vol 41 (4) ◽  
pp. 848-857 ◽  
Author(s):  
N. H. Sagert ◽  
K. J. Laidler

The kinetics of the pyrolysis of n-butane, when maximally inhibited by nitric oxide, were studied at temperatures from 540° to 610 °C, and at pressures from 30 to 550 mm Hg. The reaction has a short induction period and is accurately of the three-halves order; the activation energy was 65.9 kcal mole−1 and the frequency factor 5.3 × 1016 cc1/2 mole−1/2 sec−1. The reaction was somewhat less inhibited by surface than was the uninhibited reaction. Excess of carbon dioxide had no effect on the rate. The results are explained in terms of a free-radical mechanism for the maximally inhibited decomposition. It is proposed that the initiation step in the inhibited decomposition is mainly C4H10 + NO → C4H9 + HNO. This is followed by the ordinary chain-propagating reactions, and by processes such as C2H5 + NO → C2H5NO. The main chain-terminating step, of the type β + βNO, is concluded to be C2H5 + C2H5NO → C4H10 + NO or C2H6 + C2H4 + NO. This scheme leads to three-halves-order kinetics, and provides a satisfactory quantitative interpretation of the experimental behavior.


1963 ◽  
Vol 41 (4) ◽  
pp. 838-847 ◽  
Author(s):  
N. H. Sagert ◽  
K. J. Laidler

The kinetics of the pyrolysis of n-butane have been studied at temperatures from 520° to 590 °C, and at pressures from 30 to 600 mm Hg; the rate was followed from pressure changes and by gas chromatography. The reaction was accurately of the three-halves order; the activation energy was found to be 59.9 kcal mole−1, and the frequency factor 3.24 × 1015 cc1/2 mole−1/2 sec−1. The reaction is sensitive to surface; packing the vessel and 'conditioning' it usually led to a decrease in rate and an increase in activation energy. The reaction is concluded to be largely homogeneous, and to occur almost entirely by a free-radical mechanism; the initiation reaction is considered to be the dissociation of a butane molecule into two ethyl radicals, in its first-order region, and termination is believed to be the second-order combination of ethyl radicals. The mechanism proposed is shown to account satisfactorily for the observed behavior. The surface effect is attributed to a certain amount of initiation by abstraction, by a surface atom, of a hydrogen atom from butane, and to surface catalysis of the recombination of ethyl radicals.


2000 ◽  
Vol 127 (1) ◽  
pp. 61-72 ◽  
Author(s):  
Corwin Hansch ◽  
Susan C. McKarns ◽  
Carr J. Smith ◽  
David J. Doolittle

Author(s):  
Zhiying Fan ◽  
Zhifan Wang ◽  
Ruoyi Shi ◽  
Yuanhua Wang

Unlike C-N bond formation with classical dirhodium(II)-nitrenoids as the key intermediate, dirhodium(II)-catalyzed 1,2-and 1,3-diamination reactions are realized by a free radical mechanism. A mechanistic study revealed that the reactions undergo...


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