Photodegradation of ceftriaxone in aqueous solution by using UVC and UVC/H2O2 oxidation processes

43Citations
Citations of this article
48Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

This study investigated the performance of UVC/H2O2 and UVC processes for the degradation and mineralization of ceftriaxone as an antibiotic. The highest ceftriaxone degradation was obtained at a solution pH of 5 and H2O2 concentration of 10 mg/L. The apparent rate constant of ceftriaxone degradation was found to be 0.0302, 0.0165, and 0.0065 min−1 in the UVC/H2O2 process for the initial ceftriaxone concentrations of 5, 10, and 20 mg/L, respectively. Degradation and mineralization efficiencies of ceftriaxone was obtained to be 100% and 58%, respectively, in UVC/H2O2 process at reaction time of 120 min, whereas only 61% and 2.5% of ceftriaxone could be degraded and mineralized by UVC. The synergistic effect of UVC/H2O2 was found to be 35%. The presence of anionic species improved the photolysis efficiency which degraded ceftriaxone from 61 to 83%, while, in the UVC/H2O2 process, ability degradation declined from 100 to 70%. The efficiency of UVC/H2O2 and UVC process was not greatly affected in real tap water. Besides, the reduction patterns in the UVC/H2O2 and UVC processes were better described by pseudo-first- and second-order kinetics model with a reaction rate constant of 0.0165 and 0.0012 min−1, respectively. The rate constant of ceftriaxone degradation in the UVC/H2O2 process and at the presence of radical scavenger was found to be around 3.3 times lower than the one in its absence.

Cite

CITATION STYLE

APA

Khorsandi, H., Teymori, M., Aghapour, A. A., Jafari, S. J., Taghipour, S., & Bargeshadi, R. (2019). Photodegradation of ceftriaxone in aqueous solution by using UVC and UVC/H2O2 oxidation processes. Applied Water Science, 9(4). https://doi.org/10.1007/s13201-019-0964-2

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