Formation Of TiO Research Articles

Study of Pure and Mixed-Phase TiO2 Nanomaterials Synthesized via a Modified Solvothermal Method and Their Optical Properties

The modified-solvothermal method has been used to synthesize pure anatase and anatase-rutile mixed-phase TiO2 nanomaterials using titanium isopropoxide, sodium hydroxide, and triethylamine as primary sources with different calcination temperatures (500 °C and 700 °C). The effect of the precipitating agent, capping agent, and calcination temperatures on the properties, such as structural, morphological, and optical of the resultant nanomaterials has been investigated through several techniques including X-ray diffraction (XRD), Raman spectroscopy, Transmission electron microscopy (TEM), UV–Vis absorption spectroscopy, Scanning electron microscopy (SEM), selected area electron diffraction (SAED), and high-resolution transmission electron microscopy (HRTEM). XRD and Raman spectra confirmed the pure anatase and anatase-rutile mixed structures of the prepared nanomaterials at 500 °C and 700 °C. Furthermore, the Raman active modes confirmed the formation of TiO2. It is noticed that the crystallite size of the nanomaterials increased with increasing calcination temperature of the XRD pattern. The morphologies of the prepared samples were displayed using SEM and TEM micrographs, which are almost the same in shape (cubic and cubic rod mixed). The particle size increased with an increase in calcination temperature and was found to be between 10 and 20 nm, which is similar to the crystallite size. The lattice fringes (d) from HRTEM images are assigned to the XRD plane (101) and (110) plane of anatase and anatase-rutile TiO2, respectively. The SAED exhibited well crystalline nature and confirmed the polycrystalline nature of the prepared nanomaterials by the bright points and the ring patterns. The optical band gap decreased with an increase in temperature and the optical properties are affected by calcination temperature and triethylamine.

Tailoring β-Ti based shape memory alloy with the exceptional mechanical and functional properties towards biomedical bone implants application

In the present study, the interstitial hydrogen (H) atoms were introduced as β-stabilizing element to tailor the microstructure, martensitic phase transition, and functional properties of Ti-V-Al shape memory alloys for biomedical applications. The results revealed that the addition of interstitial H atoms into Ti-V-Al shape memory alloys induced the transition from a single αˊˊ martensite to the coexistence of β parent phase and α phase, regardless of H content. Moreover, the amount of α phase firstly increases and then decreases in the present Ti-V-Al based shape memory alloy with H content increasing. Besides, H addition resulted in larger lattice distortion, further causing the formation of nano-domains in Ti-V-Al based alloys. Besides, no endothermic and exothermic peaks were detected due to the confinement of α-phase, and the emergence of nano-domains. With increasing H atoms content, the mechanical properties such as fracture strength, hardness, recoverable strain for Ti-V-Al based shape memory alloys initially increased and then decreased. (Ti-13V-3Al)99.2H0.8 shape memory alloys exhibited the highest fracture strength of 862MPa, superior hardness of 307HV, and the fully recoverable strain under 6% pre-strain as well as the moderate elastic modulus, which was mainly attributed to the solution strengthening of interstitial H atoms and the precipitation strengthening of α phase. The best corrosion resistance of Ti-V-Al based shape memory alloys was observed with the 2.0at. % H, which was due to the formation of TiO2, Ti2O3 oxide films. Moreover, the best wear resistance with the lower wear rate of 0.9347×10-6 mm3/N mm was obtained in (Ti-13V-3Al)99.2H0.8 shape memory alloy, due to the integrated effects of higher microhardness, reinforcing effect of α phase and lubrication effect of the hydrogenated film.

Exploring Platinum Thin Films as Electrodes for High‐Temperature and ‐Pressure Electrochemical Studies in Aqueous Systems

ABSTRACTThis work reports a methodology for the fabrication of Pt thin‐film electrodes for electrochemical studies in hydrothermal systems. The research process was meticulous, with particular attention paid to the multilayer Ti/Pt/Ti/Al2O3 film structure and annealing conditions that are expected to impact the morphology of the films, surface composition and electrochemical response. The findings of this study are significant, as they provide valuable insights into the behaviour of Pt thin‐film electrodes in various media and conditions. Two different approaches were adopted for the preparation of the electrodes: in one case, the Ti/Pt/Ti/Al2O3 films deposited on sapphire wafers were exposed to rapid thermal annealing at 900°C under argon for 5 min, followed by argon ion milling to etch the final electrode pattern (Pt‐RA(900)), while in the other case, uncapped Pt films were annealed, after etching, in a tubular oven under argon at specific temperatures between 200°C and 900°C (Pt‐TO). Rapid annealing at 900°C on capped films resulted in the formation of a Pt3Ti intermetallic alloy with remarkable mechanical and chemical stability even after 10 h of immersion in deionised water, acid (0.1 M H2SO4) and alkaline media (0.1 M KOH) conditions at temperatures up to 150°C, despite the dissolution of the Al2O3 top layer at 150°C and long immersion times (> 10 h). In the case of uncapped Pt films, diffusion and oxidation of Ti through the Pt film at high temperature resulted in the formation of TiO2 on the surface of Pt. The results were confirmed by using a comprehensive suite of ex‐situ characterisation techniques to follow changes in the Pt electrode surface morphology and composition before and after immersion in H2O, 0.1 M H2SO4 and 0.1 M KOH solutions under argon. Ex‐situ electrochemical characterisation studies were also conducted to correlate the changes in the electrode surface properties, including the electrochemical surface area, with different annealing conditions and after various hydrothermal treatments in neutral, alkaline and acidic media.

Microstructure evolution and degradation process of AlCrTiSiN coatings with different Si contents at high temperatures

The microstructure evolution of AlCrTiN and AlCrTiSiN coatings containing 4, 6.8, and 10.6 at.% Si was studied at temperatures ranging from 800 to 1100 °C. The AlCrTiN coating exhibits a single-phase fcc-(Al,Cr,Ti)N structure, while the AlCrTiSiN coatings transition from a nanocomposite structure, composed of fcc-(Al,Cr,Ti)N and amorphous a-SixNy, to a fully amorphous structure as the Si content increases. The hardness and adhesion strength of coatings initially rise, peaking at 24 GPa and 44 N respectively, due to the formation of the nanocomposite structure. However, these properties decline as the coatings become fully amorphous. At elevated temperatures, severe oxidation leads to the gradual formation of layered oxides. Concurrently, phase transformation, spinodal decomposition, and crystallization occur within the nitride layer. The addition of Si enhances oxidation resistance by promoting the rapid formation of a dense and protective oxide layer, and by reducing nitrogen release and TiO2 formation. However, at 1000 and 1100 °C, the coating with 10 at.% Si exhibits slightly faster oxidation compared to the 6.8 at.% Si coating, as the increased Si content reduces the Al content, limiting the coating's ability to regenerate the protective oxide layer.

Research on corrosion behavior and biocompatibility of NiTi alloy processed with combined dealloying and annealing treatment

This paper presents a novel method to prepare hydrophilic nanoporous functional surface with combined dealloying and annealing treatment to improve the corrosion resistance and biocompatibility of NiTi components. Surface modification mechanism is discussed with microscopic characterization of NiTi nanoporous structures. Hydrophilic and biocompatible performance is achieved through specifically tailoring the dimensions and chemical compositions of nanoporous layer. The corrosion resistance of NiTi samples is investigated in 0.9 wt% NaCl solution and evaluated with potentiodynamic polarization and electrochemical impedance spectroscopy tests. The results indicate that material corrosion resistance is significantly enhanced with TiO2 formation during dealloying treatment, while annealing promotes the oxidation and densification of dealloyed layer raising the energy barrier for ion transportation during corrosion. Furthermore, as the dealloying temperature increases, the surface defects of the sample decrease resulting in better corrosion resistance. The research can provide guidance for NiTi surface modification to enhance its biomedical applications.

Exploring barium-titanium-peroxo-hydroxide as an excellent single-source precursor for crystallographically diverse barium titanate ceramics – parametric study

Barium-titanium-peroxo type amorphous materials gained importance with the advent of wet-chemical methods for the production of crystalline perovskite barium titanate (BaTiO3) electroceramics. In this paper, the chemical nature of the barium-titanium-peroxo precursor was determined by means of elemental (EPMA), spectroscopic (FT-IR and FT-Raman), XRD and thermal (DSC and TGA/DTA) analyses. Several synthesis parameters such as the barium source, the peroxide treatment time, the reaction temperature and the reaction time were investigated. The precursor was also thermally treated at varying temperatures between 30 °C and 1000 °C. Relatively high reaction temperatures are detrimental to the Ba∙O∙Ti structure, resulting in plain TiO2 formation. Though relatively low temperatures (ice bath) are needed to suppress unwanted TiOCl2, ambient synthesis conditions and short reaction time (2 h) resulted in the desired single-source properties, i.e. amorphous Ba∙O∙Ti-peroxo structure with Ba/Ti ratio of unity (1.04 ± 0.04). The addition of an extra stirring step during H2O2 addition lowered the chance of carbonate incorporation in the precursor. Thermal analysis under air and nitrogen atmosphere was performed and a stoichiometric formula of Ba2,08Ti2O(O2)1,9(OH)5,3∙3,1H2O was calculated, which was in very good agreement with literature data. The barium-titanium-peroxo-hydroxide material proved to be an excellent single-source precursor. Phase-pure, highly crystalline and facetted, stoichiometric BaTiO3 particles with differently crystallographically oriented facets were obtained via the molten-salt solid-state method ({100} or {111} oriented facets) as well as the hydrothermal route ({100} oriented facets).

Microstructure and dry sliding wear evaluation of functionally graded coating deposited via atmospheric plasma spray

Surfaces are commonly enhanced with wear-resistant coatings to improve their resistance to abrasion, erosion, and other forms of wear. These coatings play a crucial role in extending the lifespan and improving the performance of materials and components exposed to challenging conditions. The objective of the current study is to deposit thermally sprayed 3-layer TiC–12Co–10ZrO2/NiCoCrAlMo functionally graded coatings on SS410 substrates using atmospheric plasma spray. The results revealed that by employing appropriate ceramic proportions, the microhardness of graded coatings increased to 990.4 HV, which is approximately 3.21 times higher than that of the substrate. Furthermore, the tribological properties of graded coating exhibited superior resistance compared to the substrate, where process settings were varied. Specifically, graded coating samples subjected to the applied load, sliding distance, and sliding velocity showed improved wear resistance of 78.51%, 68.42%, and 76.66% respectively in extreme conditions compared with uncoated samples. The characterization of the worn surface revealed a sequential occurrence of wear mechanisms: abrasive, adhesive, and delamination. The formation of TiO2 and Cr2O3 tribo-oxide film protects the surface against the wear mechanism and is applicable in extreme wear environments.

Sunlight responsive superhydrophilic rGO-TiO2 nanocomposite coatings for photovoltaic applications

Transparent, superhydrophilic surfaces have a wide range of applications, especially for self-cleaning coatings in window panes and solar panels. Herein, reduced graphene oxide (rGO) decorated titanium dioxide (rGO-TiO2) nanocomposites (NCs) were synthesized by in-situ hydrothermal method. The X-ray diffraction and Raman spectroscopy confirmed the formation of anatase-brookite mixed phases TiO2 wherein rGO facilitates the anatase-brookite phase transformation. The NCs exhibit the transmittance of ∼79 % in the visible range and the lowest band gap of 3.03 eV. The wettability studies revealed that the films of rGO-TiO2 NCs became superhydrophilic (water contact angle <10°) upon 60 min sunlight exposure.

Solvent extraction of titanium(IV) from orthophosphoric acid media using Aliquat-336/kerosene and stripping with nitric acid

Titanium extraction from acidic solutions was investigated using Aliquat-336, considering factors like acid type and concentration for leaching, diluent type for solvent extraction, equilibration time, extractant concentration, phase ratio, and temperature. Kerosene exhibited superior performance as an aliphatic diluent for Aliquat-336 compared to other utilized diluents. The extraction efficiency was inversely proportional to the dielectric constant of the diluents. The quantitative Ti(IV) extraction efficiency from phosphoric acid (6 M H3PO4) leach liquor of ilmenite and rutile achived 98 % at room temperature (298 K) in 10 min after mixing with 0.1 M Aliquat-336 dissolved in kerosene at a phase volume ratio of 1:1 (Aq:Org). The exothermic extraction process occurred spontaneously. The proposed extraction mechanism using Aliquat-336/kerosene involves ion-pair association of the extractant with a Ti(IV) complex, confirmed by FTIR spectroscopy. The Ti(IV) ions were effectively stripped using HNO3 (3 M) with an aqueous:organic phase volume ratio of 1:1 at 25 °C after a contact time of 10 min in each step. The Aliquat-336/kerosene efficiently tested for Ti(IV) recovery from acidic Abu-Ghalaga ilmenite and rutile leachate. The findings indicate that, the phosphate medium is highly efficient in extracting Ti(IV), even with low concentration of Aliquat-336 in kerosene, especially in comparison to the impurities such as Fe, Cr, and Al. The EDX, XRD, and wet chemical analyses of the final product after the hydrolysis of stripped Ti(IV) from samples originating from the Abu-Ghalaga area and rutile samples, confirmed the formation of high-purity TiO2 (predominantly anatase phase). The SEM results showed particles with a regularly spherical structure and uniform size.

Unraveling the influence of deposited layers on Ti/RuO2 anodes to define the electroactivity of oxygen evolution and active chlorine reactions

Ti/RuO2 were synthesized using Pechini method with 4, 8 and 16-RuO2 layers, to account for the influence of their physical properties upon their behavior towards reactive oxygen evolution (OER) and active chlorine reaction (CER). Rietveld refinement conducted using X-Ray diffraction (XRD) measurements confirmed the formation of TiO2 (P42/mnm) and RuO2 (P42/mnm, poor rutile-type), which grew on a thin native TiO2 layer forming a solid solution. This analysis corroborated that the smaller RuO2 crystallite size was obtained using 4-layers, unlike the trend of increasing sizes with more layer’s numbers. This situation is not conducive to accessing reactive sites and electronic conduction issues. Interestingly, exchange current densities (j0) in NaCl(aq) presence were higher than Na2SO4(aq) for 4 and 8-layers, evidencing an inhibition of OER to catalyze CER due to RuO2. This behavior is not related to the electroactive area, since this property decreased by rising the number of layers. The 4-layers anode showed the largest production of CER after 20 min of electrolysis, but the lower accelerated lifetime (ALT). Thus, the stacking of more RuO2 layers creates a higher resistance for charge transfer. Likewise, Ti substrate is important to define the CER catalysis, whence a low coverage of RuO2 will be more catalytic than a high coverage of this oxide. The electrode activity was assessed through the removal of 132 µmol L−1 Acetaminophen (ACM), revealing that 93, 80, and 50 % was removed using 4, 8 and 16-layers of RuO2 coating respectively, at 10 mA and 0.1 molL−1 NaCl. Density functional theory (DFT) and high-performance liquid chromatograph coupled to a mass spectrometer (HPLC-MS) were used to propose a reaction mechanism for ACM degradation. Four byproducts with m/z ACM-I-1 (C8H5Cl4NO3) 304, ACM-I-2 (C8H6Cl3NO3) 274, ACM-I-3 (C6H4Cl3NO2) 227, and ACM-I-4 (C6H3Cl3O3) 229 were identified corresponding to the addition of chlorine in the amide group and aromatic ring, as a susceptible site to electrophilic attack.

Crystallographic plane-induced selective mineralization of nanohydroxyapatite on fibrous-grained titanium promotes osteointegration and biocorrosion resistance

The (002) crystallographic plane-oriented hydroxyapatite (HA) and anatase TiO2 enable favorable hydrophilicity, osteogenesis, and biocorrosion resistance. Thus, the crystallographic plane control in HA coating and crystalline phase control in TiO2 is vital to affect the surface and interface bioactivity and biocorrosion resistance of titanium (Ti) implants. However, a corresponding facile and efficient fabrication method is absent to realize the HA(002) mineralization and anatase TiO2 formation on Ti. Herein, we utilized the predominant Ti(0002) plane of the fibrous-grained titanium (FG Ti) to naturally form anatase TiO2 and further achieve a (002) basal plane oriented nanoHA (nHA) film through an in situ mild hydrothermal growth strategy. The formed FG Ti-nHA(002) remarkably improved hydrophilicity, mineralization, and biocorrosion resistance. Moreover, the nHA(002) film reserved the microgroove-like topological structure on FG Ti. It could enhance osteogenic differentiation through promoted contact guidance, showing one order of magnitude higher expression of osteogenic-related genes. On the other hand, the nHA(002) film restrained the osteoclast activity by blocking actin ring formation. Based on these capacities, FG Ti-nHA(002) improved new bone growth and binding strength in rabbit femur implantation, achieving satisfactory osseointegration within 2 weeks.

Enhancement of photocatalytic activity by thermal annealing of Au, Ag, and Cu implanted TiN thin films

The paper presents an investigation on the optoelectronic and photocatalytic properties of titanium-nitride (TiN) thin films, modified through the introduction of metal ions (Au, Ag, and Cu) during implantation, followed by thermal annealing. Employing high-resolution microscopic and spectroscopic techniques, we examined the microstructural and compositional features of the films in detail. The films exhibited a crystalline structure with distinct columnar patterns, attributed to defect release and recovery during annealing. Furthermore, metal nanoparticles were detected in samples implanted with gold and silver ions, indicating coalescence processes, while no such particles were observed in the case of Cu ions. Post-implantation annealing also led to surface oxidation and the formation of anatase TiO2, with a coexistence of TiO2, TiN, metallic Au and Ag, and CuO phases in subsurface regions. Comparative optical measurements revealed significant changes in photoluminescence efficiency and photocatalytic response of modified TiN. All implanted samples showed reduced photoluminescence intensity compared to pristine titanium-nitride, with the Au-implanted film exhibiting the most significant decrease, due to the presence of surface Au nanoparticles, thus resulting in the slower electron-hole recombination rates and enhanced photocatalytic activity.

Totally Tubular TiO2 Nanotubes as Semiconducting Material for Dye-Sensitized Photoelectrodes

The use of chemical bonds to store solar energy is a promising approach to address the intermittency of the sun by harnessing sunlight to drive chemical transformations. One strategy to drive these processes is to use a bespoke semiconductor surface implemented in a photoelectrode to absorb light and generate charge carriers that can drive redox reactions such as the direct oxidation of adsorbed species on the photoanode. To minimize recombination of photogenerated electron-hole pairs, molecular donor-chromophore-acceptor (D-C-A) systems can be used to sensitize wide bandgap semiconductors for visible light absorption and to generate (high energy) long-living charge separated states. Such assemblies represent a photoelectrode for dye-sensitized photoelectrochemical cells (DS-PECs). Presented here are recent findings using molecularly sensitized TiO2 nanotubes as a nanohybrid architecture for DS-PECs. The highly ordered and oriented 1D-nanostructures are purpose-grown using a self-organizing electrochemical anodization approach. The nanotube mouth is functionalized with a Cu(I)-based donor-chromophore-acceptor system by direct assembly at the surface. The resulting photoanodes are investigated against different water oxidation catalysts (e.g., [Cp*Ir(pyalk)OH], pyalk = 2-(pyridine-2-yl)propan-2-ol; CoOx) for their ability to generate oxidizing equivalents that can subsequently drive follow-on oxidation reactions. A more common TiO2 nanostructure morphology (e.g., nanospheres) and simpler Cu(I)-based chromophores are also examined for comparative purposes to highlight the advantages of the proposed assembly.It is well understood that the role of the semiconductor is to connect the molecular components and transfer/store charge carriers from the excited dye to drive redox processes. The TiO2 nanotubes used here are synthesized by self-organized electrochemical anodization (SOA); a process Involving an anode/cathode arrangement where Ti is used as the anode. This process is a balance between the electrochemical formation of TiO2 and simultaneous chemical dissolution in fluoride-containing electrolytes. The resulting semiconducting film is found to be a vertically oriented, size-controlled, and back-contacted nanostructured array of TiO2 on a foil of titanium. In addition to this composition inheriting high chemical stability, the morphology can grant added benefits such as two-dimensional confinement, directional charge transport and orthogonal charge separation.[1]A crucial limiting factor for the performance of this system is the recombination of the electron-hole pairs. By using a transition metal complex or chromophore (C) that is covalently linked with electron donating (D) and electron accepting (A) moieties, the energy levels can be aligned for charge-transfer processes between the electroactive groups for directional electron transport and formation of a charge-separated state.[2] Copper(I) D-C-A assemblies are also of interest when taking into consideration the low-cost and photophysical properties when compared to typical ruthenium(II) polypyridine chromophores used in these types of cells. Transient photocurrent measurements of the photoelectrode suggest that the TiO2 nanotubes’ mouths generate a base photocurrent, which could be associated with graphitic-like carbon impurities extending light absorption for photoactivity. Furthermore, once the surface is decorated with the copper(I) D-C-A assembly, the photocurrent is significantly increased, enabling light-driven oxidation of CoOx photoelectrochemically deposited on the surface of the photoelectrode.REFERENCES[1] Nguyen, N. T.; Altomare, M.; Yoo, J. E.; Taccardi, N.; Schmuki, P. Noble Metals on Anodic TiO2 Nanotube Mouths: Thermal Dewetting of Minimal Pt Co-Catalyst Loading Leads to Significantly Enhanced Photocatalytic H2 Generation. Adv. Energy Mater. 2016, 6, 1501926. DOI: 10.1002/aenm.201501926[2] Singh, Z.; Kamal, S.; Majewski, M. B. Copper(I) Donor−Chromophore−Acceptor Assembly for Light-Driven Oxidation on a Zinc Oxide Nanowire Electrode. J. Phys. Chem. C. 2022, 126, 39, 16732-16743. DOI: 10.1021/acs.jpcc.2c04652 Figure 1

Influence of pre-treatment with non-thermal atmospheric pressure plasma on bond strength of TP340 titanium-PEEK direct bonding

Direct bonding of a TP340 titanium to PEEK by hot pressing via pre-treatment of non-thermal atmospheric pressure plasma jet has been demonstrated. The plasma irradiation effect on the bonding surface on the bond strength after hot pressing was investigated. The tensile shear strength of TP340-PEEK joined by hot pressing after plasma pre-treatment was measured by comparing specimens bonded using conventional hot pressing and those bonded using adhesives. The plasma treatment to the TP340 side resulted in the formation of TiO2, which is chemically fed to oxide formation due to the irradiation of oxygen radicals generated by the plasma, resulting in a bond strength of less than 1 MPa, similar to the bond strength of the untreated specimens. The plasma irradiation effect on the PEEK side on the bond strength of TP340-PEEK bonded samples was also investigated. The bonding strength was increased by plasma irradiation to PEEK. As the plasma irradiation time was increased, the bonding strength gradually increased to 9.2 MPa, which is about 19 times higher than the bonding strength without plasma irradiation. These results suggest that oxygen radicals in the atmospheric pressure RF plasma jet produced oxygen-containing surface functional groups on the PEEK surface, which increased the strength of the TP340-PEEK direct joining.

Efficacy of mesoporous TiO2–ZrO2@g-C3N4 produced using a simple ultrasonic approach for copper ion removal from wastewater

The present study describes ultrasonically produced ternary composite material composed of carbon nitride nanosheets, zirconium, and titanium oxides for elimination of copper ions. The formation of monoclinic ZrO2, anatase TiO2, and g-C3N4 phases with respective crystallite sizes 6, 11, 13 nm were verified by the X-ray diffraction technique. The dispersion of the metal oxides nanoparticles with the graphitic nanosheets, the elemental composition of Zr, Ti, O, C and N, and the characteristic functional groups were verified respectively by TEM, EDX, and FTIR analysis that confirmed the successful formation and composition of the nanocomposite TiO2–ZrO2@g-C3N4 (TZCN). The good porosity of the composite that show a surface area, pore volume, and pore diameter values of 47.42 m2/g, 0.056 cm3 g−1, and 20.3 Å that nominate it for adsorption application. The adsorption capabilities of the nanocomposite were studied for copper ion removal from an aqueous solution, as well as the impacts of pH and starting Cu2+ concentration. The results show that the adsorption process is pH and starting concentration-dependent, with a maximum adsorption capacity of 447.8 mg/g. The Cu2+ adsorption is a monolayer chemisorption process that is well described by the Langmuir adsorption model and follows pseudo-second-order kinetics. Moreover, a plausible mechanism for Cu2+ ion adsorption on the surface of TZCN nanocomposite particles is proposed.

Designing sandwich-zigzag multilayered TiN coatings for corrosion-erosion coupling damage protection

Coatings are utilized to enhance the surface properties of materials. This study aimed to modify the TiN coating with a novel sandwich-zigzag intermediate layer and delve into the intricate damage mechanisms under harsh corrosion-erosion coupling environments. Due to the infiltration of NaCl into the coating and the subsequent formation of TiO2, the sandwich-zigzag TiN coatings exhibited a reduction in mechanical behavior and erosion resistance when exposed to salt spray at 550 °C for 50 h. Moreover, the erosion rates of the as-corroded TiN coatings displayed an opposite trend compared to that of the as-deposited coatings, showing that the erosion rate was highest at the erosion angle of 30°. Nevertheless, the presence of the zigzag-TiN intermediate layer benefited the coating by preventing stress accumulation and heterogeneous interface. This ultimately improved the erosion resistance of the coatings by more than 2 times at universal erosion angle compared to that of the substrates under the synergistic effects of corrosion and erosion.

Nanofiber array growth mechanism based on dealloying of Ti-Cu/Cu multilayer precursor film

Metal oxide nanofiber array materials are a type of material with outstanding performance and application potential. Recently, an efficient dealloying method using Ti–Cu/Cu multilayer film as a precursor was proposed to prepare titanium oxide nanofiber array structure. However, the growth mechanism and formation process of such an oxide nanofiber array grown on multilayer-film is not clear. In this work, we use Ti-Cu/Cu multilayer film as the precursor, NaOH solution as the dealloying corrosion solution, and free dealloying at room temperature. On the basis of successfully obtaining TiO2 nanofiber array films, the morphology formation and evolution process of the nanoarray were carefully monitored, and the atomic percentage changes of Ti, Cu and O elements in the dealloying precursor films were tested, as well as the formation and crystalline phase evolution trends of TiO2. Based on the experimental data, we tried to draw a schematic diagram of the formation process of this TiO2 nanofiber array, and proposed that the growth mechanism of the TiO2 nanofiber array is the precipitation growth process both with Ostwald Ripening and Oriented Attachment mechanisms. Then, the photocurrent response characteristics of the obtained nanofiber array structure samples were analyzed, and it was found that the nanofiber array structure had a certain effect on the photocurrent response performance. The completion of the present work is expected to provide a theoretical reference for the preparation and application of other metal oxide nanofiber array by dealloying method.

الفعالية المضادة لجسيمات التيتانيوم النانوية المحضرة بطريقة السول-جل لمجموعة من البكتريا السالبة و الموجبة لصبغة كرام

Titanium dioxide nanoparticles TiO2 NP were prepared by sol-gel method. TiO2 NP was identified and characterized using scanning electron microscopy (SEM), ultraviolet spectroscopy (UV-vis), Fourier transform infrared (FTIR), X-ray diffraction ( XRD) and atomic force microscopy (AFM). The SEM results showed an irregular spherical shape with different diameters (22.84-65.98) nm. The highest UV-Vis absorption was recorded at 345 nm wavelength. FTIR was used to find out the effective aggregates and the success of the process of forming TiO2 NP bands. The first centered between (450 – 800 cm-1), which is attributed to the patterns of stretching vibrations of the titanium oxide bond (Ti-O Vibrations). While the XRD peaks appeared at angles 2Ѳ (27.32°, 35.89° 39.03°, 41.02°, 43.88°, 54.09°, 56.38°, 62.43°, 63.77°, 68.67°, 69.41°, 76.11°) at Crystal Planes (110) (101) (200) (111) (210) (211) ( (220) (002) (310) (301) (112) and (202), (respectively, which corresponds to JCPDS standard tables), and this indicates the formation of rutile-type NPs TiO2. The results of (AFM) ranged between (6-7 nm) and the mean height (Z-mean value) was (8 nm). The effectiveness of NP TiO2 was tested at different concentrations (1, 0.75,0.5) mg/ml against a group of Gram-negative and Gram-positive bacteria:(Pseudomonas aeruginosa, Salmonella typhimurium, Bacillus subtilis, Staphylococcus aureus, E.coli) reached the highest zone of inhibition at a concentration of (1) mg/ml for Staphylococcus aureus, as the diameter of inhibition was (19.5).

Effect of Ti on the properties of diamond microcrystals synthesized in C–O–H supercritical fluid at high pressure and high temperature

Diamond micropowders 1–10 μm were synthesized at 7.5 GPa, 1300–1500 °C, and 3–6 s. Detonation nanodiamonds and pentaerythritol (C5H8(OH)4) with the addition of Ti were used as the reaction medium. The total nitrogen concentration, determined by electron paramagnetic resonance (EPR) and infrared (IR) spectroscopies, in diamonds synthesized without the addition of Ti was 1700 ppm. In diamonds synthesized with the addition of Ti, there are no 2N (A-center) and N3VH0 centers as well as oxygen-related functional groups, and the total concentration of nitrogen centers is reduced to 640 ppm. The addition of Ti leads to an increase in the synthesis temperature by 100–200 °C.Thermodynamics model calculations of the equilibrium compositions of the reaction medium at a pressure of 7.5. GPa and temperatures of 500, 1000 and 1500 °C were performed. The Gibbs free energy of possible reactions between the components of the reaction medium was calculated. It has been shown that under equilibrium conditions and a reaction medium corresponding to the synthesis conditions, the formation of TiN is thermodynamically possible. This leads to a decrease in the nitrogen concentration in diamonds. However, the formation of TiO2 is a competing reaction that can lead to a decrease in the concentration of oxygen-related functional groups.

Biosynthesis of titanium dioxide nanoparticles using peel extract of Parkia speciosa for methyl orange degradation

Recent research on the biosynthesisof nanoparticles has used plant rather than other biomaterials. In this work, a simpler and environmentally friendly method for the synthesis of titanium dioxide nanoparticles using Parkia speciosa peel extract (P-TiO2 NPs) was carried out. The synthesized TiO2 was characterized by XRD, FESEM, HRTEM, SAED, FTIR, UV-DRS and Zeta analyzer. The XRD and SAED data indicated the crystalline and tetragonal anatase TiO2 phase. HR-TEM and FE-SEM analysis proved that the obtained P-TiO2 had a spherical shape with nano-sized particlesof 8.56 nm. The zeta potential data showed that P-TiO2 was a stable particle. According to the FTIR spectra, the phytochemical components contained in the peel extract were responsible for the reducing and capping agents in TiO2 formation. In addition, the P-TiO2 had photocatalytic activity and completely degraded the methyl orange dye (97.99%). This study shows that the waste of Parkia speciosa could be a potential reducing and capping agents in the synthesis of TiO2 NPs for wastewater treatment.