Author/Authors :
Aguilar، C.A نويسنده Universidad Aut?noma del Carmen, Facultad de Qu?mica, Calle 56 # 4 Avenida Concordia, Ciudad del Carmen, Campeche, 24180, México , , Montalvo، C نويسنده Universidad Aut?noma del Carmen, Facultad de Qu?mica, Calle 56 # 4 Avenida Concordia, Ciudad del Carmen, Campeche, 24180, México , , Ceron، J.G نويسنده Universidad Aut?noma del Carmen, Facultad de Qu?mica, Calle 56 # 4 Avenida Concordia, Ciudad del Carmen, Campeche, 24180, México , , Moctezuma، E نويسنده Universidad Aut?noma de San Luis Potos?, Facultad de Ciencias Qu?micas, Av. Dr. Manuel Nava # 6, San Luis Potos?, S.L.P., 78290, México ,
Abstract :
The photocatalytic degradation of a common analgesic (acetaminophen) with titanium dioxide
irradiated with low energy ultraviolet light (365 nm) was studied in order to determine the effect of several
parameters such as catalyst’s weight, photochemical effect, and initial concentration. The results indicate that
acetaminophen is degraded in the order of 4% by the photochemical effect. The presence of titanium dioxide
in optimal amounts increases the rate of reaction and the overall conversion. The kinetic study demonstrated
that photocatalytic degradation of acetaminophen follows a pseudo first order reaction rate which could be
represented by a model similar to Langmuir-Hinshelwood equation. Accordingly, the results confirmed that
the degradation of acetaminophen proceeds even while other intermediate organic products (IOP) are being
formed; some of these organic products were identified by High Performance Liquid Chromatography (HPLC).
These products (OIP) remain in the solution for a while before being degraded to CO2
. Furthermore, the
experimental results indicate that the mineralization of acetaminophen can be described by an overall kinetic
rate equation obtained from the experimental values of total organic carbon (TOC).