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), 31-41. (doi:10.1016/j.jelechem.2005.10.005).
- Version of Record
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.
|Digital Object Identifier (DOI):||doi:10.1016/j.jelechem.2005.10.005|
|Keywords:||Amino acids; Disulphide adsorption; Cysteinate formation; l-cystine; l-cysteine; Mercury electrodes; Linear sweep voltammetry; Cyclic voltammetry; Polarography; HMDE; SMDE; DME|
|Subjects:||Q Science > Q Science (General)
T Technology > TP Chemical technology
Q Science > QD Chemistry
|Divisions:||University Structure - Pre August 2011 > School of Engineering Sciences > Engineering Materials & Surface Engineering
|Date Deposited:||19 Oct 2007|
|Last Modified:||31 Mar 2016 12:25|
|RDF:||RDF+N-Triples, RDF+N3, RDF+XML, Browse.|
Actions (login required)