Abstract

Rhodamine B (RhB) is a synthetic xanthine dye that is harmful to environment and human health. Therefore, the development of low cost and efficient analytical techniques for RhB monitoring is very critical for environmental protection and food safety. Herein, a novel metal-free voltammetric sensor was constructed for sensitive detection of RhB using carboxyl-functionalized carbon nanomaterials. To understand the role of carboxyl functionalization in RhB electrooxidation, the electrochemical properties and voltammetric responses of carboxyl-functionalized multi-walled carbon nanotube (f-MWCNT), carboxyl-functionalized reduced graphene oxide (f-RGO), multi-walled carbon nanotube (MWCNT) and reduced graphene oxide (RGO) were compared. Amongst, the f-MWCNT/GCE exhibited the lowest charge transferred resistance and the largest electroactive surface area. The f-MWCNT/GCE showed extraordinary electrocatalytic activity for RhB oxidation, which is primarily attributed to the unique 3D structure and the carboxyl functionalization. The anodic peak current of RhB is linearly correlated to RhB concentration from 0.05 to 100 μM with a low limit of detection (LOD, 2.6 nM). In addition, the f-MWCNT/GCE achieved the selective identification and detection of RhB in presence of common metal ions and other red dyes, and retained a robust and stable voltammetric responses for at least a week. The f-MWCNT/GCE was successfully applied to detect RhB concentration in tomato sauce samples with good recovery.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.