Log in

An alternative approach for utilizing urea as fuel source

  • Short Communication
  • Published:
Brazilian Journal of Chemical Engineering Aims and scope Submit manuscript

Abstract

In this exploratory study, an integrated electrode consisted of multi-walled carbon nanotubes (MWCNT) and urease enzyme (Ur) was used to conduct electro-catalytic oxidation of urea. The electrode was fabricated by sequential depositions of different layers of MWCNT, platinum metal, and Ur on ITO glass using mainly casting techniques. The enzyme layer was first utilized to hydrolyze urea to ammonia molecules, which was then supplied to the catalytic oxidation reaction as fuel. By doing so, the electrode was able to induce electrooxidation with a current density of 3.2 mA.cm−2 at 0.55 V obtained at urea concentration of as small as 0.1 M along with a good linearity of r2 = 0.9831.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
EUR 32.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or Ebook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price includes VAT (France)

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

References

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ly Tan Nhiem.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 193 KB)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Nhiem, L.T. An alternative approach for utilizing urea as fuel source. Braz. J. Chem. Eng. 40, 797–802 (2023). https://doi.org/10.1007/s43153-022-00277-9

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s43153-022-00277-9

Keywords

Navigation