On the Electrochemical Behavior of Pyrylium Ions at the Mercury-Electrode. III. Adsorption Behavior at the Aqueous-Mercury Interface

1987 ◽  
Vol 40 (3) ◽  
pp. 579 ◽  
Author(s):  
WNC Garrard ◽  
FG Thomas

The adsorption behaviour of four pyrylium ions-2,4,6-trimethylpyrylium, 2,4,6-tri-t- butylpyrylium , 2,4,6-triphenylpyrylium and 7-phenyl-5,6,8,9-tetrahydrodibenzo[ c,h ] xanthylium -at the mercury-aqueous 0.5 M sulfuric acid interface is reported. The 2,4,6-trimethylpyrylium ion shows little tendency to adsorb at the mercury interface even at concentrations approaching saturated solution. The tri-t- butylpyrylium ion is adsorbed in a vertical orientation on a positively charged electrode, while on a negatively charged electrode it exhibits two position adsorption- initially flat then reorienting to vertical at higher concentrations. Triphenylpyrylium ions form an adsorbed layer of vertically oriented ions which approaches monolayer coverage at potentials just prior to its reduction at -0.68 V. The product of the reduction inhibits the reduction of the parent ion. The xanthylium ion behaves in a similar manner to the tri-t-butyl ion but the conclusions are tentative due to the limited reliability of the data as a consequence of the low solubility of this ion in water.

2012 ◽  
Vol 12 (8) ◽  
pp. 3591-3599 ◽  
Author(s):  
O. Kupiainen ◽  
I. K. Ortega ◽  
T. Kurtén ◽  
H. Vehkamäki

Abstract. The substitution of ammonia by dimethylamine in sulfuric acid – ammonia – dimethylamine clusters was studied using a collision and evaporation dynamics model. Quantum chemical formation free energies were computed using B3LYP/CBSB7 for geometries and frequencies and RI-CC2/aug-cc-pV(T+d)Z for electronic energies. We first demonstrate the good performance of our method by a comparison with an experimental study investigating base substitution in positively charged clusters, and then continue by simulating base exchange in neutral clusters, which cannot be measured directly. Collisions of a dimethylamine molecule with an ammonia containing positively charged cluster result in the instantaneous evaporation of an ammonia molecule, while the dimethylamine molecule remains in the cluster. According to our simulations, a similar base exchange can take place in neutral clusters, although the overall process is more complicated. Neutral sulfuric acid – ammonia clusters are significantly less stable than their positively charged counterparts, resulting in a competition between cluster evaporation and base exchange.


Author(s):  
M. Bounoughaz ◽  
H. Boukercha ◽  
A. Khemmari ◽  
M. Allaoua ◽  
E. Salhi

CORROSION ◽  
10.5006/0709 ◽  
2013 ◽  
Vol 69 (6) ◽  
pp. 543-550 ◽  
Author(s):  
S. Jones ◽  
K. Coley ◽  
J. Kish

When exposed to concentrated sulfuric acid, stainless steel exhibits unique electrochemical behavior. This behavior can be observed as an oscillation in open-circuit potential between the active and passive states. The transient nature of the corrosion behavior under these conditions results in a distinct challenge for measuring and predicting corrosion rates. Using a series of commercial alloys with various nickel contents, this paper outlines the utilization of electrochemical experimentation to refine the prediction of corrosion rates. The paper also discusses some of the difficulties associated with many traditional electrochemical techniques such as potentiodynamic scans when used for characterizing systems that undergo oscillations in open-circuit potential.


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