The reduction of l-cystine in hydrochloric acid at mercury drop electrodes

Ralph, T.R., Hitchman, M.L., Millington, J.P. and Walsh, F.C. (2006) The reduction of l-cystine in hydrochloric acid at mercury drop electrodes Journal of Electroanalytical Chemistry, 587, (1), pp. 31-41. (doi:10.1016/j.jelechem.2005.10.005).


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The reduction of L-cystine in 0.1 mol dm3 HCl at 298 K has been studied at mercury electrodes. Dropping mercury electrode (DME), static mercury drop electrode (SMDE) and hanging mercury drop electrode (HMDE) modes were used with normal, sampled d.c. and differential pulse polarographic detection. The charge transfer kinetics for the irreversible reduction of L-cystine were complicated by reactant and product adsorption, by the formation of cysteinate complexes between mercury and the product thiol as well as by formation of Hg2Cl2. High Tafel slopes of 182 mV per decade were observed with a cathodic transfer coefficient of 0.32. The diffusion coefficient of L-cystine was found to be 5.3 · 10-10 m2 s-1 in 0.1 mol dm-3 HCl and 4.2 · 10-10 m2 s-1 in 2.0 mol dm-3 HCl at 298 K. The mechanism of L-cystine reduction at mercury has been discussed and the effects of pH and reactant concentration have been quantified.

Item Type: Article
Digital Object Identifier (DOI): doi:10.1016/j.jelechem.2005.10.005
ISSNs: 1572-6657 (print)
Keywords: Amino acids, Disulphide adsorption, Cysteinate formation, l-cystine, l-cysteine, Mercury electrodes, Linear sweep voltammetry, Cyclic voltammetry, Polarography, HMDE, SMDE, DME

Organisations: Engineering Mats & Surface Engineerg Gp
ePrint ID: 49021
Date :
Date Event
11 August 2005Submitted
3 February 2006Published
Date Deposited: 19 Oct 2007
Last Modified: 16 Apr 2017 18:20
Further Information:Google Scholar

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