In this work, metal-doped titanium dioxide (TiO2) was synthesised with the aim of improving photocatalytic degradation and antimicrobial activities; TiO2 was doped with copper (Cu) ranging from 0.1 to 1.0 wt%. The physical and chemical properties of the Cu-doped TiO2 nanoparticles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), the Brunauer–Emmett–Teller method (BET) and diffuse reflection spectroscopy (DRS). The results revealed that the anatase phase of TiO2 was maintained well in all the Cu-doped TiO2 samples. No significant difference in the particle sizes or the specific surface areas was caused by increasing Cu doping. However, the band gap decreased continuously from 3.20 eV for undoped TiO2 to 3.12 eV for 1.0 wt.% Cu-doped TiO2. In addition, the 0.1 wt.% Cu-doped TiO2 displayed a much greater photocatalytic degradation of methylene blue (MB) and excellent antibacterial ability for Escherichia coli (E. coli) compared to undoped TiO2. On the other hand, the high Cu doping levels had negative impacts on the surface charge of nanoparticles and charge transfer for OH• generation, resulting in decreasing MB degradation and E. coli photokilling for 1.0 wt.% Cu-doped TiO2.
The TiO2 nanoparticles synthesized from the extract of Coffea arabica L. (or TiO2/C) were used to remove paraquat from contaminated water in heterogeneous photocatalysis process. In this work, the sol-gel process using Coffea arabica L. as the solvent chemical were performed to obtain the TiO2 nano-catalyst. The value of pHpzc of TiO2/C was 2.9 which caused a highly acidic surface of catalyst. The paraquat is effectively removed in alkaline medium due to the adsorption ability of paraquat on the surface of TiO2/C. The paraquat degradation followed the pseudo-first-order model with the apparent rate constants of 5.84 × 10−2, 4.08 × 10−2, and 2.28 × 10−2 min−1 for TiO2/C, TiO2, and without TiO2, respectively, under the presence of ultraviolet (UV) and H2O2. The combined TiO2/C with UV and H2O2 was the most efficient process, exhibiting a maximum 66.3% degradation of 50 mg/L over 90 min at pH 10.
This work demonstrates a novel method to deposit an antibacterial TiO2 thin film on a polymer substrate at room temperature. A combination of sol–gel and photon assistance was used in the experiment in order to avoid any thermal processes of thin film crystallization. The morphological photograph of samples indicated that the TiO2 thin film was perfectly coated on the PVC substrate without any cracks or pinholes. Chemical analysis by EDS and XPS reported that the thin film consisted of titanium (Ti), oxygen (O), and carbon (C). The Raman spectrum proved that the thin film was the anatase phase of TiO2 and, furthermore, that it was contaminated with carbon remaining from the photon assistance process. In addition, the optical band gap of the thin film was 3.35 eV, suggesting that the photocatalytic activity of TiO2 should occur under UV-A radiation. The bacteria viability assay was examined using E. coli and S. typhimurium as indicator strains under UV-A irradiation (365 nm) at different times. The data from OD and CFU count revealed that >97% of bacteria were killed after 60 min of irradiation, and the bacteria were completely killed at 120 min for E. coli and 180 min for S. typhimurium.
In the present work, the photocatalytic degradation of salbutamol [2-(tert-butylamino)-1-(4-hydroxyl-3-hydroxymethylphenyl)ethanol] under visible irradiation using Mn-doped TiO2 is investigated. The Mn-doped TiO2 nanoparticles were synthesized by the sol–gel method with ratios of 0.1, 0.2, and 0.3%. Significant characteristics, including the rutile/anatase phases ratio, specific surface area, and band gap energy, were due to the amount of Mn doping; the narrowest band gap energy of 2.80 eV was observed in 0.2% Mn-doped TiO2 with specific surface areas of 89.36 m2/g and 10.87/89.13 of rutile/anatase phases. The investigation involved salbutamol photocatalytic degradation, a kinetic study, and the identification of intermediate compounds. The results indicated that 0.2% Mn-doped TiO2 obtained the best salbutamol removal of 95% under an irradiation time of 180 min. Salbutamol slowly degraded to the intermediate compounds in the first 60 min (k = 0.0088 1/min), and these intermediate compounds were dramatically mineralized to small hydrocarbon fragments and carbon dioxide in the later irradiation times (k = 0.0179 1/min). According to the high-performance liquid chromatography–mass spectrometry (HPLC-MS) results, possible degradation pathways of salbutamol were proposed: 2-(tert-butylamino)-1-(3,4-dihydroxyphenyl)ethanone, 2-(tert-butylamino)-ethanol, and 2-(tert-butylamino)-1-(4-hydroxyl-3-hydroxymethylphenyl)ethanone were initially formed and then transformed to 2-(methylamino)-1-(3,4-dihydroxyphenyl)ethanone, 2-(tert-butylamino)-acetic acid, hydroquinone, and 1-(4-hydroxylphenyl)ethanol, respectively. The mineralization of all intermediate compounds was verified by 90% chemical oxygen demand (COD) reduction, and the effluent contained a relatively low COD concentration of 7.8 mg/L.
In this present work, the photocatalytic degradation of salbutamol [2-(tert-butylamino)-1-(4-hydroxyl-3-hydroxymethylphenyl)ethanol] under visible irradiation using Mn-doped TiO2. The Mn-doped TiO2 nanoparticles were synthesized by sol-gel method with the ratio of 0.1%, 0.2% and 0.3%. The significant characteristics including rutile/anatase phase ratio, specific surface area and band gap energy was due to the amount of Mn doping; the narrowest band gap energy of 2.80 eV was observed in the 0.2% Mn-doped TiO2 with the specific surface area of 89.36 m2/g and 10.87/ 89.13 of rutile/anatase phase. The investigation involved salbutamol photocatalytic degradation, kinetic study and identification of intermediate compounds. The results indicated that the 0.2% Mn-doped TiO2 obtained the best salbutamol removal of 95% under irradiation time of 180 min. The salbutamol was slowly degraded to the intermediate compounds in the first 60 min (k = 0.0088 1/min) and they was dramatically mineralized to small hydrocarbon fragments and carbon dioxide in the later irradiation times (k = 0.0179 1/min). According to the HPLC-MS results, the possible degradation pathways of salbutamol were proposed; 2-(tert-butylamino)-1-(3,4-dihydroxyphenyl)ethanone, 2-(tert-butylamino)-ethanol and 2-(tert-butylamino)-1-(4-hydroxyl-3-hydroxymethylphenyl)ethanone were initially formed and then transformed to 2-(methylamino)-1-(3,4-dihydroxyphenyl)ethanone, 2-(tert-butylamino)-acetic acid, hydroqunone and 1-(4-hydroxylphenyl)ethanol. The mineralization of all intermediate compounds was verified by 90% of COD reduction and the effluent contained relatively low COD concentration of 7.8 mg/L.
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