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Synthesizing and Evaluating the Photocatalytic and Antibacterial Ability of TiO₂/SiO₂ Nanocomposite for Silicate Coating.

ABSTRACT: The TiO₂/SiO₂ nanocomposite has been synthesized by a sol-gel method and investigated the effect of the SiO₂ content (0, 5, 10, 15, 20, and 50%) on the rutile-to-anatase phase transition of TiO₂ NPs. In order to increase the photocatalytic efficiency of the nanocomposite and decrease the price of material, the TiO₂/SiO₂ Nc with content SiO₂ of 15% sample is chosen for preparing silicate coating. The efficiency of photocatalytic MB and antibacterial ability in the air of W silicate coating (adding TiO₂/SiO₂ Nc (15%)) achieve almost 100% for 60 h and 94.35% for 3 h, respectively. While the efficiency of photocatalytic MB and antibacterial ability of WO silicate coating (adding commercial TiO₂/SiO₂) is about 25-30% for 60 h and 6.02% for 3 h, respectively. The presence of TiO₂/SiO₂ Nc (15%) with a larger surface area in W silicate coating can provide increased centers for absorption, photocatalytic reaction, and the contact between sample and bacteria lead to enhance the photocatalytic and antibacterial ability of W silicate coating.

SUBMITTER: Le MC

PROVIDER: S-EPMC8485069 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:In this article, the TiO2/SiO2-np nanocomposite multilayer films were synthesized in a single step by reactive magnetron sputtering combined with a nanoparticle aerosol jet. The SiO2 nanoparticles (SiO2-np) were introduced into a growing TiO2 thin film with different time sequences during deposition for a fixed duration. The SiO2-np acting as impurities are introduced into the TiO2 to willingly disturb its growth and to cause growth defects in order to increase the specific surface area of the photocatalytic film. In reason of the non-photoactive properties of the SiO2 nanoparticles, their introduction allows us to study only the effects induced on the film morphology, microstructure, and photocatalytic properties by their incorporation. The fractographies and topographies reveal strong changes in the morphologies depending on the time sequence of the nanoparticle introduction in the thin films. The introduction of SiO2-np from the beginning of the TiO2 film growth leads to the formation of high and large growth defects resulting in a highly diffusive surface. In addition, XRD analysis shows that the crystallite size tends to decrease as the composite film layer gets closer to the surface. Their photocatalytic performance is obtained by following the degradation of orange G dye under UV-visible irradiation. The photocatalytic performance is not only related to the specific surface area of the catalyst film, and the coverage of the photoactive phase on the surface, but also to the crystal quality of the photoactive phase. Furthermore, the samples exhibit good photostability, maintaining the same activity after four degradation cycles. In the specific case of TiO2/SiO2-np, it is demonstrated that the introduction of the nanoparticles only at the beginning of the film growth is more efficient than a continuous introduction. This result suggests that this original process allows the use of a relevant strategy for the nanoparticle introduction according to the required functionality.

Project description:Water scarcity is now a serious global issue resulting from population growth, water decrease, and pollution. Traditional wastewater treatment plants are insufficient and cannot meet the basic standards of water quality at reasonable cost or processing time. In this paper we report the preparation, characterization and multiple applications of an efficient photocatalytic nanocomposite (CoxNi1-xFe2O4; x?=?0.9/SiO2/TiO2/C-dots) synthesized by a layer-by-layer method. Then, the photocatalytic capabilities of the synthesized nanocomposite were extensively-studied against aqueous solutions of chloramine-T trihydrate. In addition, reaction kinetics, degradation mechanism and various parameters affecting the photocatalytic efficiency (nanocomposite dose, chloramine-T initial concentration, and reaction pH) were analyzed in detail. Further, the antimicrobial activities of the prepared nanocomposite were tested and the effect of UV-activation on the antimicrobial abilities of the prepared nanocomposite was analyzed. Finally, a comparison between the antimicrobial abilities of the current nanocomposite and our previously-reported nanocomposite (CoxNi1-xFe2O4; x?=?0.9/SiO2/TiO2) had been carried out. Our results revealed that the prepared nanocomposite possessed a high degree of crystallinity, confirmed by XRD, while UV-Vis. recorded an absorption peak at 299 nm. In addition, the prepared nanocomposite possessed BET-surface area of (28.29?±?0.19 m2/g) with narrow pore size distribution. Moreover, it had semi-spherical morphology, high-purity and an average particle size of (19.0 nm). The photocatalytic degradation efficiency was inversely-proportional to chloramine-T initial concentration and directly proportional to the photocatalyst dose. In addition, basic medium (pH 9) was the best suited for chloramine-T degradation. Moreover, UV-irradiation improved the antimicrobial abilities of the prepared nanocomposite against E. coli, B. cereus, and C. tropicalis after 60 min. The observed antimicrobial abilities (high ZOI, low MIC and more efficient antibiofilm capabilities) were unique compared to our previously-reported nanocomposite. Our work offers significant insights into more efficient water treatment and fosters the ongoing efforts looking at how pollutants degrade the water supply and the disinfection of water-borne pathogenic microorganisms.

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Synthesizing and Evaluating the Photocatalytic and Antibacterial Ability of TiO₂/SiO₂ Nanocomposite for Silicate Coating.

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Synthesizing and Evaluating the Photocatalytic and Antibacterial Ability of TiO2/SiO2 Nanocomposite for Silicate Coating.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets

Synthesizing and Evaluating the Photocatalytic and Antibacterial Ability of TiO₂/SiO₂ Nanocomposite for Silicate Coating.