KMITL
Permanent URI for this communityhttps://dspace.kmitl.ac.th/handle/kmitl/1
Browse
2 results
Search Results
- Some of the metrics are blocked by yourconsent settings
Item type:Publication, Study of ni2+/ni3+ redox couple and electrocatalytic responses of ni on nitrogen-doped carbon for urea non-enzymatic detection(2021-01-01) ;Asavakijthananont, NaraweeJanyasupab, MetiniA novel redox couple of metallic nickel (Ni) catalyst can become a great candidate of non-enzymatic detection. By taking advantage of fast electron transfer, Ni redox couples can be tailored as pseudo-enzyme in urea measurement. In this study, Ni catalyst on nitrogen doped carbon (Ni-NC) was synthesized and characterized morphological, elemental, and electrocatalytic properties in comparison to different configuration of pure nickel (Ni), Ni with carbon (Ni-C), and bare carbon electrode, assessed by cyclic voltammetry and differential pulse voltammetry. By examining various Ni redox couples in rapid electron transfer process, the prominent anodic and cathodic peaks of Ni<sup>2+</sup>/Ni<sup>3+</sup> were applicable to detect urea in the detection range of 1-20 mM, with an excellent sensitivity and relative standard deviation of 1.634 µA.mM<sup>-1</sup> (R<sup>2</sup> of 0.989) and 4.89%, respectively. Therefore, Ni-NC can find practical applications for material sensing device toward non-enzymatic urea measurement. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Development of wireless based potentiostat in biomedical applications(2019-03-01) ;Janyasupab, MetiniAsavakijthananont, NaraweeWirelessly integrated and portable electronics designs of analytical systems are of great importance to support future technological platforms including internet of things (IoT), artificial intelligence (AI), precision medicine, and wearable chemical/biological sensing systems. In this study, a simple and robust prototype of the so-called potentiostat, electrochemical instrumental system, with a wireless data acquisition and user control is demonstrated. With a wide range of potential applications, the developed system can be conveniently customizable to detect chemical of interest in food safety, continuous at-home diagnosis, environmental monitoring, and low-power energy storage. The device is comprised of two major units: a modified front-end sensor (Texas Instrument, LMP91000EVM), and a development board (Espressif, ESP32) implementing with a programmable saw tooth waveform to assess cyclic voltammetry (CV), the most common electrochemical measurement with the three-electrode configuration, namely working electrode, reference electrode and auxiliary electrode. In particular, the prototype shows a good agreement of CV in a standard electron transfer experiment by monitoring the interchange state of Fe<sup>2+</sup> and Fe<sup>3+</sup> ion in ferricyanide solution with potassium chloride supported, in comparison to that of the commercial potentiostat. Furthermore, the effects of different scan rate (0.05 to 0.15 V/s) and different ferricyanide concentrations from 1 to 7.5 millimolar are also evaluated to quantify sensing performance. Based on the obtained results, the calibration curve of anodic peak and cathodic peak current are linearly correlated with R<sup>2</sup> of 0.9987 and 0.9990, respectively, providing a cost-effective (less than USD 80) and portable solution to the future integration of sensing technology.
