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In this study, Fe- and Ag-modified TiO2 nanotubes were synthesized via an anodization method as photocatalysts for degradation of polyethylene microplastics and disinfection of Escherichia coli (E. coli). The anodization voltage, as well as the Fe3+ or Ag+ concentrations on TiO2 nanotubes were evaluated and correlated to their corresponding photocatalytic properties. TiO2 nanotubes were firstly synthesized by anodization of Ti plates in a glycerol-based electrolyte, followed by incorporation of either Fe or Ag via a Successive Ionic Layer Adsorption and Reaction (SILAR) method with Fe(NO3)3 and AgNO3 as Fe and Ag precursors, respectively. UV-Vis DRS shows that the addition of Fe or Ag on TiO2 nanotubes causes a redshift in the absorption spectra. The X-ray diffractograms indicate that, in the case of Fe-modified samples, Fe3+ was successfully incorporated into TiO2 lattice, while Ag scatters around the surface of the tubes as Ag and Ag2O nanoparticles. A microplastic degradation test was carried out for 90 mins inside a photoreactor with UVC illumination. TiO2 nanotubes that are anodized with a voltage of 30 V exhibit the best degradation results with 17.33% microplastic weight loss in 90 mins. Among the modified TiO2 nanotubes, 0.03 M Ag-TiO2 was the only one that surpassed the unmodified TiO2 in terms of microplastic degradation in the water, offering up to 18% microplastic weight loss in 90 min. In terms of E. coli disinfection, 0.03M Ag-TiO2 exhibit better performance than its unmodified counterpart, revealing 99.999% bactericidal activities in 10 mins. Copyright © 2022 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). 

Background: Whether nanoengineered titanium surfaces confer superior implant stability beyond modern microrough controls remains uncertain. Methods: This systematic review followed PRISMA 2020 guidance: comprehensive multi-database searching with de-duplication; dual independent screening, full-text assessment, and standardized data extraction for predefined outcomes (implant stability quotient [ISQ], mechanical anchorage by removal/push-out/pull-out torque, and histologic bone-to-implant contact). Risk of bias was appraised with RoB 2 for randomized trials, ROBINS-I for non-randomized clinical studies, and CAMARADES (animal experimentation). The certainty of clinical evidence was summarized using GRADE. Results: Across animal models, nanoengineered surfaces consistently improved early osseointegration indices (higher removal torque and bone-to-implant contact at initial healing). In clinical comparative studies, nanoengineered implants showed modest, time-limited gains in early stability (ISQ) versus microrough titanium. By 3–6 months, between-group differences typically diminished, and no consistent advantages were demonstrated for survival or marginal bone outcomes at later follow-up. Methodologic heterogeneity (surface chemistries, timepoints, outcome definitions) and small clinical samples limited quantitative synthesis. Overall, risk-of-bias concerns ranged from some concerns to high in non-randomized studies; the certainty of clinical evidence was low. Conclusions: Nanofeatured titanium surfaces improve early osseointegration but do not demonstrate a consistent long-term advantage over modern microrough implants. Current evidence supports an early osseointegration benefit without clear long-term clinical advantage over contemporary microrough implants. Adequately powered, head-to-head trials with standardized stability endpoints and ≥12-month follow-up are needed to determine whether early gains translate into patient-important outcomes.

With the introduction of a new interdisciplinary field, osteoimmunology, today, it is well acknowledged that biomaterial-induced inflammation is modulated by immune cells, primarily macrophages, and can be controlled by nanotopographical cues. Recent studies have investigated the effect of surface properties in modulating the immune reaction, and literature data indicate that various surface cues can dictate both the immune response and bone tissue repair. In this context, the purpose of the present study was to investigate the effects of titanium dioxide nanotube (TNT) interspacing on the response of the macrophage-like cell line RAW 264.7. The cells were maintained in contact with the surfaces of flat titanium (Ti) and anodic TNTs with an intertube spacing of 20 nm (TNT20) and 80 nm (TNT80), under standard or pro-inflammatory conditions. The results revealed that nanotube interspacing can influence macrophage response in terms of cell survival and proliferation, cellular morphology and polarization, cytokine/chemokine expression, and foreign body reaction. While the nanostructured topography did not tune the macrophages’ differentiation into osteoclasts, this behavior was significantly reduced as compared to flat Ti surface. Overall, this study provides a new insight into how nanotubes’ morphological features, particularly intertube spacing, could affect macrophage behavior.

We successfully synthesised TiO2 nanotubes (TNTs) and silver nanoparticles (Ag NPs)-loaded TiO2 nanotubes paste. These were coated on a glass substrate by spin coating method, and their antibacterial activities were surveyed. The morphology of materials was defined by transmission electron microscopy (TEM) image; the crystalline structure and the composition of the materials were determined by X-ray diffraction (XRD) pattern and X-ray photoelectron spectroscopy (XPS). Vibrational properties of the molecules existing in the sample were investigated by Fourier transform infrared (FTIR) spectroscopy, and the transmittances of films were determined by UV–Vis transmittance spectroscopy. This research shows that the structure and morphology of TNTs did not change after they underwent the processes of paste preparing and film coating on a glass substrate. Furthermore, the transmittance of TNTs film (about 75%) is higher than Ag NPs-loaded TiO2 nanotubes (Ag/TNTs) film (about 65%) in the visible region. Moreover, the antibacterial property of Ag/TNTs film shows its effectiveness against Escherichia coli bacteria, and the antibacterial efficiency is 99.06% for 24 h-incubation period in the dark condition.

Titanium oxide (TiO2) nanotubes (TNTs) have been successfully formed by anodisation of pure Titanium (Ti) foil in an electrolyte consisting of 85 % glycerol with varying amount of NH4F. Organic electrolyte was used to produce longer nanotubes with higher energy conversion efficiencies during photoelectrochemical. The effect of NH4F and time for TNTs formation during anodisation was studied. The optimised amount of NH4F was 0.7 g and anodisation time required for a complete dissolution was more than 15 min. This condition will produce adequate surface etching and inwards growth to occur. The comparison of photocurrent density between irregular and well organised TNTs was investigated. Photocurrent density enhancement was also observed. TNTs photocurrent density was 60% higher as compared to nanoporous TiO2. The photoelectrochemical response of the TNTs photoelectrode was studied by using 1 M KOH solution under Xe lamp illumination.

Nanoporous/nanotubular complex oxide layers were developed on high-fraction β phase quaternary Ti-Nb-Zr-Ta and Ti-Nb-Zr-Fe promising biomedical alloys with a low elasticity modulus. Surface modification was achieved by electrochemical anodization aimed at the synthesis of the morphology of the nanostructures, which exhibited inner diameters of 15–100 nm. SEM, EDS, XRD, and current evolution analyses were performed for the characterization of the oxide layers. By optimizing the process parameters of electrochemical anodization, complex oxide layers with pore/tube openings of 18–92 nm on Ti-10Nb-10Zr-5Ta, 19–89 nm on Ti-20Nb-20Zr-4Ta, and 17–72 nm on Ti-29.3Nb-13.6Zr-1.9Fe alloys were synthesized using 1 M H3PO4 + 0.5 wt% HF aqueous electrolytes and 0.5 wt% NH4F + 2 wt% H20 + ethylene glycol organic electrolytes.

Hydrogen production from water splitting by photo/photoelectron‐catalytic process is a promising route to solve both fossil fuel depletion and environmental pollution at the same time. Titanium dioxide (TiO2) nanotubes have attracted much interest due to their large specific surface area and highly ordered structure, which has led to promising potential applications in photocatalytic degradation, photoreduction of CO2, water splitting, supercapacitors, dye‐sensitized solar cells, lithium‐ion batteries and biomedical devices. Nanotubes can be fabricated via facile hydrothermal method, solvothermal method, template technique and electrochemical anodic oxidation. In this report, we provide a comprehensive review on recent progress of the synthesis and modification of TiO2 nanotubes to be used for photo/photoelectro‐catalytic water splitting. The future development of TiO2 nanotubes is also discussed. Hydrogen production from water splitting by photo/photoelectron‐catalytic process is one promising route to solve both energy depletion and environmental pollution at the same time. Titanium dioxide (TiO2) nanotubes have attracted much interest and show potential applications in photocatalytic degradation, water splitting and lithium‐ion batteries etc. In this review, the recent progress of TiO2 nanotubes in the synthesis processes and modification used to improve the performance of photo/photoelectrocatalytic water splitting is comprehensively reviewed. The future development of TiO2 nanotubes is also briefly discussed and addressed.

Adjusting the Schottky barrier height is an important approach to enhancing the gas-sensing performance of TiO2 Schottky sensors. In this study, micro TiO2 nanotube Schottky sensors were fabricated via magnetron sputtering and anodic oxidation, with their Schottky barrier height adjusted by varying the annealing temperature. The morphology, phase composition, oxygen vacancy concentration, band structure, and Schottky junction of the samples were investigated using SEM, GIXRD, EPR, Hall effect measurements, XPS, I-V curves, and AC impedance. The sensor annealed at 500 °C demonstrated the highest gas-sensing response, outperforming sensors treated at other temperatures by over 100 times. Its response value to 1 ppm H2 was 242. The annealing temperature significantly affects the TiO2 phase and oxygen vacancy concentration, resulting in the highest Schottky barrier height in the 500 °C-annealed sensor, which contributes to its superior sensing performance. AC impedance measurements revealed no significant Fermi-level pinning in TiO2. Based on the gas-sensing mechanism analysis, the response of the TiO2 sensor can be divided into three regimes: Schottky junction control, TiO2 resistance control, and co-control.

The selective photocatalytic oxidation with O2 as oxidant of valencene and thymol was evaluated using nanostructured TiO2 under UV-Vis radiation at atmospheric conditions. The effect of the morphology and optical properties of TiO2 nanotubes and aminate nanoparticles was studied. Different scavengers were used to detect the presence of positive holes (h+), electrons (e−), hydroxyl radicals (•OH), and the superoxide radical anion (O2−) during the photooxidation reaction. Superoxide anion radical is the main oxidizing specie formed, which is responsible for the selective formation of nootkatone and thymoquinone using aminated TiO2 nanoparticles under 400 nm radiation.