Application of nano electrode Ag/AgCl on potentiometric sensor based on molecularly imprinted polymer (MIP) to verify caffeine

3Citations
Citations of this article
11Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Caffeine of Molecularly Imprinted Polymer (MIP) has been synthesized by the cooling-heating method and to obtain sensor material to detect caffeine. The caffeine is verified through a potentiometric method based on galvanic cells involving anodes and cathodes. MIP of caffeine that has been made function as a cathode or working electrode and the modified of the Ag/AgCl reference electrode that made by reducing the AgCl membrane to nano size (44.45 nm) function as an anode. Then the modified Ag/AgCl reference electrode performance test is compared to the standard AgCl reference electrode. The result has shown the modified Ag/AgCl reference electrode produces linearity of the calibration curve in testing caffeine solutions with a concentration range of 0.1 ppm to 5.0 ppm. Based on the result of the modified Ag/AgCl reference electrode's test range, we got the linearity coefficient value of 0.9993, with a slope of 0.9693 and an intercept of 0.1306. Generated accuracy calculation resulted in a value of 98.85% and a precision of 0.951%. The result of the lower limit of detection (LoD) was at a concentration of 0.2 ppm and the limit of quantification (LoQ) at a concentration of 0.4 ppm. Thus, it concluded that the modified Ag/AgCl reference electrode has the same or equivalent capability as a standard electrode.

Cite

CITATION STYLE

APA

Yanto, F., Royani, I., & Suheryanto. (2021). Application of nano electrode Ag/AgCl on potentiometric sensor based on molecularly imprinted polymer (MIP) to verify caffeine. In Journal of Physics: Conference Series (Vol. 1751). IOP Publishing Ltd. https://doi.org/10.1088/1742-6596/1751/1/012074

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free