Journal
ELECTROANALYSIS
Volume 20, Issue 22, Pages 2395-2402Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/elan.200804338
Keywords
Voltammetry; SDS; Sodium dodecylsulfate; Chitosan; Sisal; Textile; Cellulose; Diffusion; Triclosan; Electrochemistry; Sensors
Categories
Funding
- Driving Innovation in Chemistry and Chemical Engineering (DICE) Science and Innovation Award [EP/D501229/1]
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Glassy carbon electrodes are modified with a thin film of a cellulose-chitosan nanocomposite. Cellulose nanofibrils (of ca. 4 run diameter and 250 nm length) are employed as an inert backbone and chitosan (poly-D-glucosamine, low molecular weight, 75-85% deacetylated) is introduced as a structural binder and receptor or molecular binding site. The composite films are formed in a solvent evaporation method and prepared in approximately 0.8 mu m thickness. The adsorption of three molecular systems into the cellulose-chitosan films is investigated and approximate Langmuirian binding constants are evaluated: i) Fe(CN)(6)(4-) (K-Ferrocyanide = 2.2 x 10(3) mol(-1) dm(3) in 0.1 M phosphate buffer at pH 6) is observed to bind to ammonium chitosan functionalities (present at pH < 7), ii) triclosan (K-Triclosan = 2.6 x 10(3) mol(-1) dm(3) in 0.1 M phosphate buffer pH 9.5) is shown to bind only weakly and under alkaline conditions, and iii) the anionic surfactant dodecylsulfate (K-SDS = 3.3 x 10(4) mol(-1) dm(3) in 0.1 M phosphate buffer pH 6) is shown to bind relatively more strongly in acidic media. The competitive binding of Fe(CN)(6)(4-) and dodecylsulfate anions is proposed as a way to accumulate and indirectly determine the anionic surfactant.
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