Photocatalytic degradation of Pharmaceutical Compounds in Wastewater using Doped TiO2-SiO2 Photocatalyst
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Abstract
India, a developing country, has surpassed the United States as the world's third largest producer
of pharmaceutical drugs. The consumption of pharmaceuticals and personal care products (PPCPs)
have increased dramatically in recent years. The concentration of PPCPs in the environment is
typically extremely low, ranging from ngL-1
to gL-1
. Toxic nature of these substances and
persistence in the environment have sparked widespread concern among societies and regulatory
bodies around the world. Advanced Oxidation Processes (AOPs) such as photocatalysis have
gained widespread popularity among researchers because of their ability to treat a wide range of
pollutants.
Pharmaceuticals have been detected in ground water, surface water, ocean, sediments, and soil.
The detected compounds included antibiotics, antihistamines, anticonvulsants, painkillers,
hormones, cytostatic drugs, lipid regulators, beta-blockers, and X-ray contrast media that are
potentially harmful to the living being. According to present status of COVID-19 coronavirus,
various antibiotics have sparked as potential COVID-19 treatment options in the year 2020. The
huge demand and consumption of DOX and OFL, its incomplete metabolism and complex
behavior in the atmosphere are causing a great ecological issue, which needs to be solved.
In this regard, researchers have chosen Advanced oxidation processes (AOPs), which are
extremely promising methods for the treatment of contaminated wastewaters containing non-
biodegradable organic pollutants.Titanium dioxide has been established as the most active
photocatalyst for the breakdown of organic molecules among numerous semiconductor materials.
Because of its high efficiency, low cost, chemical, and physical stability, broad availability, and
noncorrosive nature, Undoubtedly, TiO2 photocatalysis has established its reputation in the field
of advanced wastewater treatment, but recombination of electrons and holes has always been a
matter of concern when considering its commercial applications. High band gap energy (3.2 eV)
enables TiO2 to absorb only UV light and limits its solar light application. Unfortunately, low
surface area, aggregation and the difficulty in product recovery often limit its practical application.
To overcome these limitations, many surface modification methods have been conceived. TiO2-
SiO2 oxides have been widely employed as photocatalysts, displaying outstanding efficiency in
the removal of highly hazardous and non-biodegradable contaminants such as dyes, phenols, and
benzenes from wastewater .
TiO2 modification using SiO2 alone is insufficient to maximise TiO2 use in a solar light powered
wastewater treatment process. As a result, in order to directly utilise the energy from sunlight, the
third material must have a low band-gap energy (Eg < 3). The absorption edge of TiO2-SiO2 was
roughly 400 nm, but doping techniques elevate the activity of nano-doped TiO2 from the UV region
to the visible light region. The development of novel catalysts with high-efficiency photocatalytic
performance under solar light is therefore of great significance for removal of the pharmaceutical
compounds and further improve the pilot photocatalytic performance.
In the present study, best efforts have been made to overcome these hurdles by doping and
codoping TiO2-SiO2 photocatalyst with iron and copper metal ions. This will help in the
advancement of ongoing efforts to prepare modified photocatalysts to enhance their solar light
activity. This research proposes a water purification strategy that is efficient, clean, and recyclable
for the removal of antibiotic contaminants. The main focus was to degrade different
pharmaceutical drugs like Doxycycline (DOX), Amoxicillin (AMX), Ofloxacin (OFLX), and
Cetirizine using the TiO2-SiO2 based photocatalysis.
The synthesised photocatalyst was characterised for its physical and chemical properties using
different characterization techniques such as, XRD, FTIR, DRS, FESEM, TEM, RS, and BET.
The photocatalytic experiments were investigated under visible, UV, and solar light (on sunny
days). The prepared undoped, doped, and codoped TiO2-SiO2 nano photocatalyst were used in the
photocatalytic degradation of AMX, CTZ, DOX, and OFLX. Photocatalytic experiments were
performed in a shallow pond slurry reactor made of borosilicate glass under continuous magnetic
stirring. The concentration of antibiotics were measured continuously using a UV-Vis
spectrophotometer. Effect of various parameters like time, solution pH, catalyst loading, dopant
concentration, intensity of light and A/V ratio were studied on the degradation efficiency of
antibiotics. The concentration of OH• radicals was determined, as well as its role in the
photocatalytic degradation of drugs. Moreover, to check the durability of the photocatalyst, the
lifetime of the catalyst was investigated, because it gives an impact on cost-effectiveness. Radical
trapping experiments were conducted to assess the contribution of •OH radicals, h
+
, O2, and (•O2-
) generated during solar light irradiation. The mineralization of the compounds AMX, OFLX,
CTZ, and DOX were confirmed in terms of reduction TOC.
Experimentally it was determined that synthesized photocatalyst could degrade model pollutant
compounds excellently due to its large surface area and high separation efficiency of photo-
generated carriers with high oxidation and reduction capabilities. The photocatalytic reusability
was investigated for up to several successive cycles, and the composite particles maintained their
high photodegradation activity for DOX and OFLX. Out of the various prepared catalysts, TSFC1
performed best without the oxidants, depicted good stability, and did not lose significant activity
after re-use till seven cycles. The total cost, reaction rate, and recyclability studies confirmed that
TSFC1 is a promising catalyst for photocatalytic degradation of selected compounds. Moreover,
the appropriate dopant amount in TiO2-SiO2 was conducive to enhancing the sunlight
photocatalytic activity proposing a promising environmentally compatible technology.
