V S Muralidharan
Articles written in Journal of Chemical Sciences
Volume 103 Issue 6 December 1991 pp 753-761 Physical and Theoretical
Porous iron electrodes containing metal additives have been used in nickel-iron cells. The impedances of these electrodes were measured over a wide range of frequency 104 Hz to 10−2 Hz in 6 M KOH + 0·63 M LiOH solutions. Using a cylindrical pore model, porosity and its related parameters were calculated. It is found that Hg and S provide favourable porosity and thus enhance the discharge capacity.
Volume 107 Issue 5 October 1995 pp 581-591 Physical And Theoretical
Cyclic voltammetric studies were carried in mixtures of SnSO4 and ZnSO4 containing sodium gluconate in the
Volume 108 Issue 4 August 1996 pp 399-405 Physical And Theoretical
2-Carboxy ethyl phosphonic acid (2-CEPA) in the presence of Zn2+ ions synergistically inhibits mild steel corrosion in 60 ppm chloride solutions. Calcium gluconate (CG) enhances inhibition. Electrochemical and weight change methods are used to study synergistic inhibition, and the mechanism of inhibition is discussed.
Volume 108 Issue 4 August 1996 pp 407-413 Physical And Theoretical
2-Carboxy ethyl phosphonic acid (2-CEPA) in presence of zinc ions synergistically inhibits mild steel corrosion in 60 ppm chloride solutions. Addition of calcium gluconate provides enhanced inhibition. Spectrochemical analyses of the solution and the surface inhibitor film reveal the presence of Zn (OH)2 and iron phosphono gluconate complex.
Volume 111 Issue 2 April 1999 pp 377-386 Physical And Theoretical
Cyclic voltammetric measurements were made on pure copper, nickel and 70/30 copper-nickel alloy in sodium sulphate and sodium chloride (0.5 M) solutions. In sodium sulphate solution the passivation of copper and nickel is through oxide formation. The passive film on copper nickel alloy is found to have nickel ions ingress along with copper oxide by volume diffusion. Nickel ions cause hindrance to the reduction of copper oxide to copper. The presence of chloride ions increases the dissolution of nickel while copper is passivated. The formation of CuCl2 and its subsequent hydrolysis to hydroxide prevents the dissolution. Introduction of nickel in copper depassivates the copper and hydrolysis of monovalent copper complex is prevented by the ingress of nickel ions. The formation of NiCl2 along with CuCl2 is facilitated by chloride ions.
Volume 113 Issue 1 February 2001 pp 63-76
Cupronickels offer enhanced corrosion protection in marine environments by the formation of passive films on the surface. Cyclic voltammetric studies were carried on cupronickels in chloride solutions at pH 6.3 to understand the role of chloride ions in passive film formation. Increase in nickel content of the alloy and of chloride ions in solution decreases film resistance. Chloride ions take part in reduction of the passive film to copper. A solid-state model for passive film formation involving chloride ions has been attempted.
Volume 134, 2022
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