Research

Electrochemical and sonoelectrochemical monitoring of indigo reduction by glucose


Reference:

Vuorerna, A., John, P., Keskitalo, M., Kulandainathan, M. A. and Marken, F., 2008. Electrochemical and sonoelectrochemical monitoring of indigo reduction by glucose. Dyes and Pigments, 76 (2), pp. 542-549.

Related documents:

This repository does not currently have the full-text of this item.
You may be able to access a copy if URLs are provided below. (Contact Author)

Abstract

The reduction of indigo (dispersed in water) to leuco-indigo (dissolved in water) is an important industrial process and investigated here for the case of glucose as an environmentally benign reducing agent. In order to quantitatively follow the formation of leuco-indigo two approaches based on (i) rotating disk voltammetry and (ii) sonovoltammetry are developed. Leuco-indigo, once formed in alkaline solution, is readily monitored at a glassy carbon electrode in the mass transport limit employing hydrodynamic voltammetry. The presence of power ultrasound further improves the leuco-indigo determination due to additional agitation and homogenization effects. While inactive at room temperature, glucose readily reduces indigo in alkaline media at 65 degrees C. In the presence of excess glucose, a surface dissolution kinetics limited process is proposed following the rate law d eta(leuco-indigo)/dt = k x c(OH-) x S-indigo where eta(leuco-indigo) is the amount of leuco-indigo formed, k = 4.1 x 10(-9) m s(-1) (at 65 degrees C, assuming spherical particles of I gm diameter) is the heterogeneous dissolution rate constant,c(OH-) is the concentration of hydroxide, and Sindigo is the reactive surface area. The activation energy for this process in aqueous 0.2 M NaOH is E-A = 64 U mol(-1) consistent with a considerable temperature effects. The redox mediator 1,8-dihydroxyanthraquinone is shown to significantly enhance the reaction rate by catalysing the electron transfer between glucose and solid indigo particles. (c) 2006 Elsevier Ltd. All fights reserved.

Details

Item Type Articles
CreatorsVuorerna, A., John, P., Keskitalo, M., Kulandainathan, M. A. and Marken, F.
DOI10.1016/j.dyepig.2006.06.044
DepartmentsFaculty of Science > Chemistry
RefereedYes
StatusPublished
ID Code4453
Additional InformationID number: ISI:000250292600038

Export

Actions (login required)

View Item