Comparative Study on UV-AOPs for Efficient Continuous Flow Removal of 4-tert-Butylphenol

In the present study, UV-light-driven advanced oxidation processes (AOPs) have been employed for the degradation of 4-tert-Butylphenol (4-t-BP) in water under continuous flow conditions. The effects of varying space time (10, 20, 40, 60 and 120 min) and oxidant dosage (88.3 mg/L, 176.6 mg/L and 264 mg/L) were examined. 4-t-BP degradation efficiency in the UV-induced AOPs followed the order of UV/H2O2 (264.9 mg/L) ≈ UV/Fe2+/H2O2 > UV/Fe3+/H2O2 > UV/H2O2 (176.6 mg/L) > UV/H2O2 (88.3 mg/L) > UV/Fe-TiO2 > UV/TiO2 > UV, while UV/Fe3+/H2O2 was the most efficient process in terms of Total Organic Carbon (TOC) removal (at the space time of 60 min) among those tested. The combination of UV with 88.3 mg/L H2O2 enhanced pollutant removal from 51.29% to 93.34% after 10 min of irradiation. The presence of H2O2 contributed to the highest 4-t-BP and TOC removal values. Interestingly, the increase in space time from 20 to 60 min resulted in surpassing of the activity of the Fe-TiO2 over commercial TiO2, although it had an almost negligible positive impact on the performance of the UV/H2O2 system as well as H2O2 concentration. The results obtained showed that more than 80% of 4-t-BP could be successfully degraded by both heterogeneous and homogeneous AOPs after 60 min.

Kinetics and Mechanism of Aniline and Chloroanilines Degradation Photocatalyzed by Halloysite-TiO2 and Halloysite-Fe2O3 Nanocomposites

The kinetics of photocatalytic degradation of aniline, 2-chloroaniline, and 2,6-dichloroaniline in the presence of halloysite-TiO2 and halloysite-Fe2O3 nanocomposites, halloysite containing naturally dispersed TiO2, Fe2O3, commercial TiO2, P25, and α-Fe2O3 photocatalysts, were investigated with two approaches: the Langmuir–Hinshelwood and first-order equations. Adsorption equilibrium constants and adsorption enthalpies, photodegradation rate constants, and activation energies for photocatalytic degradation were calculated for all studied amines photodegradation. The photodegradation mechanism was proposed according to organic intermediates identified by mass spectrometry and electrophoresis methods. Based on experimental results, it can be concluded that after 300 min of irradiation, aniline, 2-chloro-, and 2,6-dichloroaniline were completely degraded in the presence of used photocatalysts. Research results allowed us to conclude that higher adsorption capacity and immobilization of TiO2 and Fe2O3 on the halloysite surface in the case of halloysite-TiO2 and halloysite-Fe2O3 nanocomposites significantly increases photocatalytic activity of these materials in comparison to the commercial photocatalyst: TiO2, Fe2O3, and P25.

Highly Active TiO2 Photocatalysts for Hydrogen Production through a Combination of Commercial TiO2 Material Selection and Platinum Co-Catalyst Deposition Using a Colloidal Approach with Green Reductants

In this contribution, four different commercial TiO2 catalysts (P25, P90, PC105, and PC500) were screened for the photocatalytic production of hydrogen using ethanol as the sacrificial agent. The physico-chemical properties of the TiO2 powders were characterized by using different methods. The photocatalysts mainly vary in the ratio of anatase and rutile phases, and in the surface area. It was found that the photocatalytic activity is governed by the surface area of the photocatalyst. Pure TiO2,PC500 showed the best performance, and in comparison to P25, the activity was more than ten times higher due to its high surface area of about 270 m2 g−1. For further improvement of the photocatalytic activity, platinum nanoparticles (PtNPs) were immobilized onto TiO2,PC500 using two methods: a colloidal approach and a photodeposition method. For the reduction of the platinum salt precursor in the colloidal approach, different green reducing agents were used in comparison to ascorbic acid. The obtained platinum nanoparticles using natural reductants showed a higher photocatalytic activity due to the formation of smaller nanoparticles, as proven by transmission electron microscopy (TEM). The highest activity was obtained when mangosteen was used as the green reducing agent. Compared to ascorbic acid as a classical reducing agent, the photocatalytic activity of the Pt@TiO2,PC500 prepared with mangosteen was about 2–3 times higher in comparison to other as-prepared photocatalysts. The Pt@TiO2,PC500 catalyst was further studied under different operating conditions, such as catalyst and sacrificial agent concentration.

Electrochemical Generation of Hydrogen and Methanol using ITO Sheet Decorated with Modified-Titania as Electrode

Current issues of global warming and environmental pollution due to extensive use of fossil fuels has been reached to an alarming position. Being CO2 as main byproduct of fossil fuel consumption and water as abundantly available on earth surface has great potential to replace fossil fuels as energy source. Herein, electrocatalytic CO2 reduction with water for methanol and hydrogen gas (H2) production over ITO sheet decorated with modified-Titanium nanorods (TiO2 NR), has been investigated. The performance comparison of electrocatalytic activity of hydrothermally modified-titania with commercial TiO2 microparticles (MP) were further investigated. Electrochemical reactor containing KHCO3 aqueous solution with CO2 as an electrolyte and modified TiO2 nanorods (NR) as working electrodes offer an eco-friendly system to produce clean and sustainable energy system. The typical rates of product, i.e. methanol and H2 generation from the ITO sheet decorated with modified TiO2 NR layer recorded higher than those for the ITO sheet with commercial TiO2 microparticle. At 2.0V applied potential vs Ag/AgCl as reference electrode, the modified TiO2 NR electrocatalyst yielded methanol at a rate of 3.32 µmol.cm−2.L−1 and H2 at a rate of 6 µmol.cm−2.L−1 which was higher than that of commercial TiO2 MP electrocatalyst (methanol = 1.5 µmol.cm−2.L−1 and H2 = 3.7 µmol.cm−2.L−1). The enhancement in product yields of methanol and H2 was mainly due to the notable improvements and modification in texture of TiO2 working electrode interface. Hence, it is concluded that the modified TiO2 NR can be considered as a competent candidate for sustainable energy conversion applications. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

Mesoporous titania nanoparticles as photocatalyst for degradation of 2-chlorophenol

Mesoporous titania nanoparticles (MTN) was successfully prepared by microwave-assisted menthod. The performance of MTN was compared with degussa P25 (commercial TiO2) on photocatalytic degradation of 2-chlorophenol (2-CP). Both catalysts were characterized by XRD, FTIR, UV-Vis DRS and surface area analysis. The characterization data indicated that MTN has higher surface area and lower particle size than P25. The 2-CP was successfully degraded completely under UV light irradiation despite of having a slightly higher band-gap value compared with P25. This study demonstrated that MTN shows a good potential as a photocatalyst.

Characterization of Commercial TiO2 P90 Modified with ZnO by the Impregnation Method

This article is devoted to TiO2/ZnO nanocomposites’ creation by modifying with the commercial TiO2/P90 product using the impregnation method and identifying the effect of the ZnO modifier on its adsorption, structural, photocatalytic, and electrical properties. The synthesized TiO2/ZnO nanocomposites were characterized by XRD, XRF, XPS, and low-temperature nitrogen adsorption-desorption methods. As a result, nanostructured TiO2/ZnO composites with the ZnO content of 2, 5, 10, and 15% were obtained. It was shown that the phase composition of TiO2/P90 does not change during the nanocomposite synthesis. XPS studies of TiO2/ZnO nanocomposites indicated the presence of Ti4+, Zn2+, O2−, and OH states on their surface, which is associated with TiO2, ZnO, and hydroxide ions. The nitrogen adsorption-desorption method showed that the commercial TiO2/P90 sample is nonporous, and all TiO2/ZnO nanocomposites are characterized by almost the same homogeneous mesoporous structure. Experimentally established sorption and photocatalytic properties depend on the specific surface area and electrostatic interaction with dyes. The effect of the ZnO modifier on I-V characteristics of the TiO2/P90 sample was revealed. The obtained experimental data showed that the TiO2/P90 sample contains one type of current carriers, and TiO2/2ZnO and TiO2/5ZnO nanocomposites are characterized by two types of current carriers.

Photocatalytic and UV-VIS Optical Properties of Titanium-Silver Doped Composite Synthesized by Hydrothermal Method

Titanium (TiO2) has been studied and proved to be the most ideal photocatalyst due to several aspects such as high photoactivity, thermal and chemical stability, relatively inexpensive and non-toxicity. As the problem statement, the photoactivity and optical stability are the crucial aspects to synthesize an ideal photocatalyst. These aspects can be improved through the synthesize method to enhance its nanocrystal crystallinity. The purpose of this research is to synthesize the high crystalline silver-titanium (AgTiO2) nanoparticles and study its photoactivity and optical properties. The Ag-TiO2 was synthesized through the modification of caustic hydrothermal method and molten salt doping process to dope the silver nitrate (AgNO3) as a dopant agent. The photoactivity performance of high grade TiO2 and high crystallinity Ag-TiO2 were examine via a Methylene Blue Degradation (MBD) testing under both visible light and UV light. The optical properties were measured through the Surface Area BET (SBET) and UV-Vis-NIR spectrophotometer (UV-Vis). The UV-Vis results show that the 0.01%-Ag-TiO2 sample has a lowest band gap with 2.6eV compared to the commercial TiO2 (P25) and other samples. The SBET analysation shows that, the biggest surface area was formed in 0.05%-Ag-TiO2 followed by 0.01%-Ag-TiO2, un-doped TiO2 and 0.03%-Ag-TiO2. For the MBD-testing, the high crystalline Ag-TiO2 was performed a better photoactivity compared to the high grade TiO2. The 0.05%-Ag-TiO2 has the best crystallinity and morphology growth compared to 0.01%-Ag-TiO2 and 0.03%-Ag-TiO2 doping samples. The results obtained proves that, the presence of silver dopants was successfully improved the nanocrystal crystallinity of Ag-TiO2 and influenced its photoactivity performance.