Search Results (88)

This narrative review explores the role of additive manufacturing (AM) technologies in the production of dental implants, focusing on materials and key AM methods. The study discusses several materials used in implant fabrication, including porous titanium, trabecular tantalum, zirconium dioxide, polymers, and composite materials. These materials are evaluated for their mechanical properties, biocompatibility, and suitability for AM processes. Additionally, the review examines the main AM technologies used in dental implant production, such as selective laser melting (SLM), electron beam melting (EBM), stereolithography (SLA), selective laser sintering (SLS), and direct metal laser sintering (DMLS). These technologies are compared based on their accuracy, material limitations, customization potential, and applicability in dental practice. The final section presents a data source analysis of the Web of Science and Scopus databases, based on keyword searches. The analysis evaluates the research trends using three criteria: publication category, document type, and year of publication. This provides an insight into the evolution and current trends in the field of additive manufacturing for dental implants. The findings highlight the growing importance of AM technologies in producing customized and efficient dental implants. Full article

The increasing demand for titanium implants necessitates improved longevity. Plasma-sprayed hydroxyapatite coatings enhance implant osseointegration but are susceptible to delamination. Alternatively, anodized hydroxyapatite coatings have shown greater adhesion strengths. The present study aimed to develop anodized hydroxyapatite coatings on titanium using commercial calcium-fortified fruit juice as a calcium source. Varying the electrolyte compositions enabled the formation of four oxide groups with different predominate calcium compounds. Each oxide’s morphology, crystallinity, chemistry, molecular structure, and adhesion quality were compared and contrasted. Nanoscale SEM images revealed a progression from porous surface oxide to white surface deposits to petal-like hydroxyapatite structures with the changing anodization electrolytes. Oxide thickness evaluations showed progression from a single-layered oxide with low Ca-, P-, and Mg-dopant incorporations to bi-layered oxide structures with increased Ca-, P-, and Mg-dopant incorporation with changing electrolytes. The bi-layered oxide structures exhibited a titanium-dioxide-rich inner layer and calcium-compound-rich outer layers. Furthermore, indentation analyses confirmed good adhesion quality for three oxides. For the predominate hydroxyapatite oxides, FTIR analyses showed carbonate substitutions indicating the presence of bone-like apatite formation, and ICP-OES analyses revealed prolonged Ca and Mg release over 30 days. These Mg-enhanced carbonated apatite coatings show much promise to improve osseointegration and future implant lifetimes. Full article

The morphology of Poly (vinylidene fluoride) (PVDF) membranes prepared via the nonsolvent-induced phase separation (NIPS) method was modulated by altering the dope solution with citric acid (CA) and titanium dioxide nanoparticles (nano-TiO₂) to optimize the β-phase content. Three series of dope solutions were prepared in dimethyl acetamide (DMAc): (i) TONx series contained 0.0–10% citric acid, (ii) Mx series contained 0.0–0.4% nano-TiO₂, and (iii) TAx series contained 5% CA and 0.0–0.40% nano-TiO₂. A field emission scanning electron microscopy (FESEM) study revealed that CA enhances pore opening, and nano-TiO₂ transforms the sponge-like uneven porous structures into a compact, relatively regular honeycomb structure in the PVDF membranes. The combined effect of CA and nano-TiO₂ in the dope solution made the channels and chambers of the membrane well organized, and the walls of the channels transformed from solid fibrils to cross-woven nanofiber-like entities. Porosity initially peaked at 84% in the TAx series, gradually decreasing to 72% with increasing nano-TiO₂ concentrations. X-ray diffraction (XRD), Fourier-Transformed Infrared Spectroscopy (FTIR), and Differential Scanning Calorimetry (DSC) revealed the presence of a combined relative amount of the β- and γ-polymorphs of 84% in a neat PVDF membrane, 88% in an Mx, and 96% in a TAx series membrane, with the β-PVDF constituting nearly the entire portion of the combined polymorphs. The presence of 96% electroactive polymorph content in the PVDF membrane is noteworthy, highlighting its potential biomedical and industrial applications. Full article

Novel AB-Polybenzimidazole (AB-PBI)/TiO₂ nanocomposite membranes have been prepared using a synthetic green chemistry approach. Modified Eaton’s reagent (methansulfonic acid/P₂O₅) was used as both reaction media for microwave-assisted synthesis of AB-PBI and as an efficient dispersant of partially agglomerated titanium dioxide powders. Composite membranes of 80 µm thickness have been prepared by a film casting approach involving subsequent anti-solvent inversion in order to obtain porous composite membranes possessing high sorption capacity. The maximal TiO₂ filler content achieved was 20 wt.% TiO₂ nanoparticles (NPs). Titania particles were green synthesized (using a different content of Mentha Spicata (MS) aqueous extract) by hydrothermal activation (150 °C), followed by thermal treatment at 400 °C. The various methods such as powder X-ray diffraction and Thermogravimetric analyses, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy and Energy-dispersive X-ray spectroscopy, Electronic paramagnetic resonance, Scanning Electron Microscopy and Transmission Electron Microscopy have been used to study the phase and surface composition, structure, morphology, and thermal behavior of the synthesized nanocomposite membranes. The photocatalytic ability of the so-prepared AB-Polybenzimidazole/bio-TiO₂ membranes was studied for decolorization of Reactive Black 5 (RB5) as a model azo dye pollutant under UV light illumination. The polymer membrane in basic form, containing TiO₂ particles, was obtained with a 40 mL quantity of the MS extract, exhibiting the highest decolorization rate (96%) after 180 min of UV irradiation. The so-prepared AB-Polybenzimidazole/TiO₂ samples have a powerful antibacterial effect on E. coli when irradiated by UV light. Full article

Toxic heavy metal ions, such as lead ions, significantly threaten human health and the environment. This work introduces a novel method for the simple and sensitive detection of lead ions based on biochar-loaded titanium dioxide nanoparticles (BC@TiO₂NPs) nanocomposites. Eco-friendly biochar samples were prepared from spent coffee grounds (500 °C, 1 h) that were chemically activated with TiO₂ nanoparticles (150 °C, 24 h) to improve their conductivity. Structural characterizations showed that BC@TiO₂NPs have a porous structure. The BC@TiO₂NPs material was evaluated for lead ion determination by assembling glassy carbon electrodes. Under optimal conditions, the sensor was immersed in a solution containing the analyte (0.1 M NaAc-HAc buffer, pH = 4.5) for the detection of lead ions via differential pulse voltammetry. A linear dynamic range from 1 pM to 10 μMwas achieved, with a detection limit of 0.6268 pM. Additionally, the analyte was determined in tap water samples, and a satisfactory recovery rate was achieved. Full article

In recent years, slippery liquid-infused porous surfaces (SLIPSs) have gained significant attention in antifouling applications. However, their slippery performance often deteriorates in dynamic environments, limiting their service life. TC4 titanium alloy, commonly used in hulls and propellers, is prone to biofouling. SLIPSs have gained significant attention in antifouling applications. However, their slippery performance often deteriorates in dynamic environments, limiting their service life. To address these issues, a novel slippery liquid-infused surface (STASL) was developed on TC4 through the integration of hydroxyl end-blocked dimethylsiloxane (OH-PDMS), a silane coupling agent (KH550), and nano-titanium dioxide loaded with silver particles (TiO₂-Ag, anatase) and silicone oil, thereby ensuring stable performance in both dynamic and static conditions. The as-prepared surfaces exhibited excellent sliding capabilities for water, acidic, alkaline, and saline droplets, achieving speeds of up to 2.859 cm/s. Notably, the STASL demonstrated superior oil retention and slippery stability compared to SLIPS, particularly at increased rotational speeds. With remarkable self-cleaning properties, the STASL significantly reduced the adhesion of proteins (50.0%), bacteria (77.8%), and algae (78.8%) compared to the titanium alloy. With these outstanding properties, the STASL has emerged as a promising solution for mitigating marine biofouling and corrosion on titanium alloys. Full article

Titanium dioxide (TiO₂) is widely employed in the catalytic degradation of wastewater, owing to its robust stability, superior photocatalytic efficiency, and cost-effectiveness. Nonetheless, isolating the fine particulate photocatalysts from the solution post-reaction poses a significant challenge in practical photocatalytic processes. Furthermore, these particles have a tendency to agglomerate into larger clusters, which diminishes their stability. To address this issue, the present study has developed Al₂O₃–SiO₂–TiO₂ composite semiconductor porous ceramics and has systematically explored the influence of Al₂O₃ and SiO₂ on the structure and properties of TiO₂ porous ceramics. The findings reveal that the incorporation of Al₂O₃ augments the open porosity of the ceramics and inhibits the aggregation of TiO₂, thereby increasing the catalytic site and improving the light absorption capacity. On the other hand, the addition of SiO₂ enhances the bending strength of the ceramics and inhibits the conversion of anatase to rutile, thereby further enhancing its photocatalytic activity. Consequently, at an optimal composition of 55 wt.% Al₂O₃, 40 wt.% TiO₂, and 5 wt.% SiO₂, the resulting porous ceramics exhibit a methylene blue removal rate of 91.50%, and even after undergoing five cycles of testing, their catalytic efficiency remains approximately 83.82%. These outcomes underscore the exceptional photocatalytic degradation efficiency, recyclability, and reusability of the Al₂O₃–SiO₂–TiO₂ porous ceramics, suggesting their substantial potential for application in the treatment of dye wastewater, especially for the removal of methylene blue. Full article

We report a study on the SnS_x (x < 1) decoration of porous TiO₂ nanoparticle thin films using the ionic layer adsorption and reaction (ILAR) method. UV-vis absorption measurements revealed a direct bandgap of 1.40–2.10 eV for SnS_x (with x = 0.85) and 3.15 eV for TiO₂. Degradation of rhodamine B molecules in aqueous solutions shows that coating with a Sn-to-Ti molar ratio of 2% improves the efficiency of the photocatalytic performance of titanium dioxide, but excessive coverage decreases it. We interpret the observed behavior as due to a delicate balance of many competing factors. The formation of intimate interfaces guaranteed by the ILAR growth technique and a nearly optimal alignment of conduction band edges facilitate electron transfer, reducing electron–hole recombination rates. However, the valence hole transfer from TiO₂ to SnS reduces the oxidative potential, which is crucial in the degradation mechanism. Full article

Refractory materials are used worldwide in process equipment. However, gaseous and liquid process products penetrate the surface layer and deep into the volume of refractories, destroying rather expensive constructions that are complicated to repair. To address this challenge, there is a need to develop protective coatings for refractory materials that can limit the penetration of working media and extend their operational lifespan. In this work, the application of gas-dynamic cold spraying (CGDS) to produce a coating on the refractory materials using fine titanium dioxide (TiO₂) particles is explored. These particles are accelerated within a nitrogen flow, passing through a Laval nozzle, and then sprayed onto a fireclay surface. The mechanisms of particle deposition and layer formation on porous surfaces through experiments and numerical simulations were investigated. The geometry of a typical refractory pore was determined, which was then incorporated into computational fluid dynamics (CFD) simulations to model the cold spraying process of porous substrates. As a result, the influence of the particle size on its velocity and angle of penetration into pores was established. Experimental findings demonstrate the effective closure of pores and the formation of a particle layer on the refractory surface. Furthermore, the nanoindentation tests for the refractory samples showcase capabilities for checking coating thickness for porous materials. Full article

A strong alkaline catalyst, sodium methoxide (CH₃ONa), is commonly used to catalyze the transesterification reaction for biodiesel production. Meanwhile, titanium dioxide (TiO₂) anatase with a bandgap of 3.2 eV is a highly competitive photocatalyst after the absorption of sufficient energy from ultraviolet light. There has been no published report on the synergistic catalyst effects of CH₃ONa and TiO₂ on further facilitating the transesterification reaction. Hence, an impregnating method was used in this study to prepare the heterogeneous photocatalyst comprising TiO₂ nanoparticles embedded with a CH₃ONa catalyst. The TiO₂ nanoparticles were first immersed in an aqueous solution of CH₃ONa so that CH₃ONa could diffuse into the interior surfaces of the TiO₂ porous structure. The mixture of TiO₂ and CH₃ONa was then calcined in the temperature range from 150 °C to 450 °C for 4 h to produce the TiO_2/CH₃ONa photocatalyst. Various characteristics of the catalyst were analyzed to determine the optimum preparation conditions. The Fourier transform infrared spectroscopy spectra revealed that the absorption peaks of CH₃ONa appeared in the wavelength range of 600 cm⁻¹ and 1500 cm⁻¹. The X-ray diffractometer analysis showed that the calcined CH₃ONa did not alter the crystal structure of the catalyst carrier TiO₂. At the calcined temperatures between 100 °C and 800 °C, no intermediate or pyrolyzed product of CH₃ONa was detected, as revealed by the thermogravimetric analyzer spectra. In addition, about 5~9 wt.% elemental calcium in the CH₃ONa solution could be calcined onto the surface of TiO₂. In addition, the FTIR spectra confirmed the successful sintering and bonding of CH₃ONa onto the TiO₂ nanoparticles. The energy dispersive spectrometry result revealed that the interior surface of the TiO₂ nanoparticles was filled with the CH₃ONa compound. Full article

A cellulose-based carbon aerogel (CTN) loaded with titanium dioxide (TiO₂) and graphitic carbon nitride (g-C₃N₄) was prepared using sol–gel, freeze-drying, and high-temperature carbonization methods. The formation of the sol–gel was carried out through a one-pot method using refining papermaking pulp, tetrabutyl titanate, and urea as raw materials and hectorite as a cross-linking and reinforcing agent. Due to the cross-linking ability of hectorite, the carbonized aerogel maintained a porous structure and had a large specific surface area with low density (0.0209 g/cm³). The analysis of XRD, XPS, and Raman spectra revealed that the titanium dioxide (TiO₂) and graphitic carbon nitride (g-C₃N₄) were uniformly distributed in the CTN, while TEM and SEM observations demonstrated the uniformly distributed three-dimensional porous structure of CTN. The photocatalytic activity of the CTN was determined according to its ability to degrade rhodamine B. The removal rate reached 89% under visible light after 120 min. In addition, the CTN was still stable after five reuse cycles. The proposed catalyst exhibits excellent photocatalytic performance under visible light conditions. Full article

Understanding of dusty fluids for different Brinkman numbers in porous media is limited. This study examines the Darcy–Brinkman model for two-dimensional magneto-hydrodynamic fluid flow across permeable stretching/shrinking surfaces with heat transfer. Water was considered as a conventional base fluid in which the copper (Cu), silver (Ag), and titanium dioxide ($Ti{O}_2$) nanoparticles were submerged in a preparation of a ternary dusty nanofluid. The governing nonlinear partial differential equations are converted to ordinary differential equations through suitable similarity conversions. Under radiation and mass transpiration, analytical solutions for stretching sheets/shrinking sheets are obtained. Several parameters are investigated, including the magnetic field, Darcy–Brinkman model, solution domain, and inverse Darcy number. The outcomes of the present article reveal that increasing the Brinkman number and inverse Darcy number decreases the velocity of the fluid and dusty phase. Increasing the magnetic field decreases the momentum of the boundary layer. Ternary dusty nanofluids have significantly improved the heat transmission process for manufacturing with applications in engineering, and biological and physical sciences. The findings of this study demonstrate that the ternary nanofluid phase’s heat and mass transpiration performance is better than the dusty phase’s performance. Full article

This study proposes synthesis and evaluation of gelatin-/alginate-based hydrogel scaffolds reinforced with titanium dioxide (TiO₂) nanoparticles which, through their combination with allantoin, quercetin, and caffeic acid, provide multi-target therapy directed on all phases of the wound healing process. These scaffolds provide the simultaneous release of bioactive agents and concurrently support cell/tissue repair through the replicated structure of a native extracellular matrix. The hydrogel scaffolds were synthesized via a crosslinking reaction using EDC as a crosslinker for gelatin. Synthesized hydrogel scaffolds and the effect of TiO₂ on their properties were characterized by structural, mechanical, morphological, and swelling properties, and the porosity, wettability, adhesion to skin tissue, and simultaneous release features. The biocompatibility of the scaffolds was tested in vitro on fibroblasts (MRC5 cells) and in vivo (Caenorhabditis elegans) in a survival probe. The scaffolds revealed porous interconnected morphology, porosity of 88.33 to 96.76%, elastic modulus of 1.53 to 4.29 MPa, full hydrophilicity, favorable skin adhesivity, and biocompatibility. The simultaneous release was investigated in vitro indicating dependence on the scaffold’s composition and type of bioactive agents. The novel scaffolds designed as multi-target therapy have significant promise for improved wound healing in a beneficial and non-invasive manner. Full article

This study focuses on the surface modification of Ti₆Al₄V scaffolds produced through additive manufacturing using the Powder-Bed Fusion Electron-Beam Melting (PBF-EB) technique. From our perspective, this technique has the potential to enhance implant osseointegration, involving the growth of a layer of titanium dioxide nanotubes (TiO₂) on surfaces through anodic oxidation. Scaffolds with anodized surfaces were characterized, and the formation of a nanoporous and crystalline TiO₂ layer was confirmed. The analysis of cell morphology revealed that cells adhered to the anodized surfaces through their filopodia, which led to proliferation during the initial hours. However, it was observed that the adhesion of Saos-2 cells was lower on anodized scaffolds compared to both built and chemically polished scaffolds throughout the cell culture period. The results obtained here suggest that while anodic oxidation is effective in achieving a nanoporous surface, cell adhesion and interaction were affected by the weak adhesion of cell filopodia to the surface. Thus, combining surface treatment techniques to create micro- and nanopores may be an effective alternative for achieving a favorable cellular response when the objective is to enhance the performance of porous titanium scaffolds in the short term. Full article

This work aims to enhance the dye-removal performance of prepared poly(acrylic acid-co-acrylamide)-modified, deproteinized, natural rubber ((PAA-co-PAM)-DPNR) through incorporation with silver nanoparticles/titanium dioxide. The (PAA-co-PAM)-DPNR was prepared by emulsion-graft copolymerization with a grafting efficiency of 10.20 ± 2.33 to 54.26 ± 1.55%. The composites based on (PAA-co-PAM)-DPNR comprising silver nanoparticles and titanium dioxide ((PAA-co-PAM)-DPNR/Ag-TiO₂) were then prepared by latex compounding using the fixed concentration of AgNO₃ (0.5 phr) and varying concentrations of TiO₂ at 1.0, 2.5, and 5.0 phr. The formation of silver nanoparticles was obtained by heat and applied pressure. The composites had a porous morphology as they allowed water to diffuse in their structure, allowing the high specific area to interact with dye molecules. The incorporation of silver nanoparticles/titanium dioxide improved the compressive modulus from 1.015 ± 0.062 to 2.283 ± 0.043 KPa. The (PAA-co-PAM)-DPNR/Ag-TiO₂ composite with 5.0 phr of TiO₂ had a maximum adsorption capacity of 206.42 mg/g, which increased by 2.02-fold compared to (PAA-co-PAM)-DPNR. The behavior of dye removal was assessed with the pseudo-second-order kinetic model and Langmuir isotherm adsorption model. These composites can maintain their removal efficiency above 90% for up to five cycles. Thus, these composites could have the potential for dye-removal applications. Full article