A new method for surface modification of TiO2/Al2O3 nanocomposites with enhanced anti-friction properties

In this paper, the TiO₂/Al₂O₃ composite nanoparticles were prepared by a hydrothermal method and in situ modified with acrylic acid. It was found that the mean particle size of modified TiO₂/Al₂O₃ composite nanoparticles was about 80 nm with a uniform distribution by the particle size analysis. The modified TiO₂/Al₂O₃ composite nanoparticles can disperse in lubricating oil homogenously for several weeks. The dispersion stabilization of modified TiO₂/Al₂O₃ composite nanoparticles in lubricating oil was significantly improved in comparison with the as-prepared nanoparticles, which was due to the introduction of grafted polymers by surface modification. The formation of covalent bands was identified by Fourier transform infrared spectrum. Under an optimized concentration of 0.1 wt%, the averaged friction coefficient was reduced by 14.75%, when the modified TiO₂/Al₂O₃ composite nanoparticles were used as lubricating oil additivities.     

Preparation and hydrophilicity of TiO2 sol-gel derived nanocomposite films modified with copper loaded TiO2 nanoparticles

In this study, TiO₂ nanocomposite films with 10 g/L of TiO₂ and copper loaded TiO₂ nanoparticles as nanofillers were deposited on the glass substrates using the sol gel dip-coating method. FE-SEM and UV-vis spectrophotometer were used to evaluate morphological and optical properties of copper loaded titania nanoparticles. In addition, XPS and water contact angle techniques were used to study the surface properties and superhydrophilicity of titania nanocomposite films, respectively. The results indicated that copper loaded TiO₂ nanoparticles had a significant effect on the hydrophilicity of nanocomposite film and maintaining it in a dark place for a long time (6.2 degree for titania nanocomposite films with copper loaded nanoparticle and 23.7 degree for nanocomposite film with titania nanoparticles).     

CO2 bubble absorption enhancement in methanol-based nanofluids

In this study, the nanoparticles (i.e. SiO₂ and Al₂O₃ nanoparticles) and methanol are combined into SiO₂/methanol and Al₂O₃/methanol nanofluids to enhance the CO₂ absorption rate of the base fluid (methanol). The absorption experiments are performed in the bubble type absorber system equipped with mass flow controller (MFC), mass flow meter (MFM) and silica gel (which can remove the methanol vapor existing in the outlet gases). The parametric analysis on the effects of the particle species and concentrations on CO₂ bubble absorption rate is carried out. The particle concentration ranges from 0.005 to 0.5 vol%. It is found that the CO₂ absorption rate is enhanced up to 4.5% at 0.01 vol% of Al₂O₃/methanol nanofluids at 20 °C, and 5.6% at 0.01 vol% of SiO₂/methanol nanofluids at −20 °C, respectively.     

Enhancing tensile/compressive response of magnesium alloy AZ31 by integrating with Al2O3 nanoparticles

AZ31 nanocomposite containing Al₂O₃ nanoparticle reinforcement was fabricated using solidification processing followed by hot extrusion. The Al₂O₃ nanoparticle reinforcement was isolated prior to melting by wrapping in Al foil of minimal weight (<0.50 wt% with respect to AZ31 matrix weight). The AZ31 nanocomposite exhibited slightly smaller grain and intermetallic particle sizes than monolithic AZ31, reasonable Al₂O₃ nanoparticle distribution, non-dominant (0 0 0 2) texture in the longitudinal direction unlike monolithic AZ31, and 30% higher hardness than monolithic AZ31. Compared to monolithic AZ31, the AZ31 nanocomposite exhibited higher 0.2%TYS, UTS, failure strain and work of fracture (WOF) (+19%, +21%, +113% and +162%, respectively). Also, compared to monolithic AZ31, the AZ31 nanocomposite exhibited higher 0.2%CYS and UCS, similar failure strain, and higher WOF (+5%, +5%, −4% and +11%, respectively). Inclusive of crystallographic texture changes, the effect of Al₂O₃ nanoparticle integration on the enhancement of tensile and compressive properties of AZ31 is investigated in this paper.     

Growth mode transition of atomic layer deposited Al2O3 on porous TiO2 electrodes of dye-sensitized solar cells

This study investigates the growth behavior of atomic-layer-deposited (ALD) Al₂O₃ overlayers on porous TiO₂ electrodes, which comprise an anatase nanoparticle layer and a rutile particle layer, for optimizing dye-sensitized solar cells. The growth mode of the ALD Al₂O₃ overlayers changes from island growth to layer-by-layer growth during the first few ALD reaction cycles, and the growth mode transition is much more pronounced for the anatase electrode layer. The transition is likely a result of the reduction in the contractive lattice strain of the TiO₂ nanoparticles. The lattice strain in the hydroxylated TiO₂ nanoparticles is progressively reduced during the ALD Al₂O₃ deposition, resulting in the growth mode transition.     

Enhanced photoelectrochemical properties and photocatalytic activity of porous TiO2 films with highly dispersed small Au nanoparticles

Small Au nanoparticles (NPs) with mean diameter of 4.1 nm were highly deposited on TiO₂ films via a simple electrostatic self-assembly method. The physically separated Au NPs, with a high surface density of 6.3 × 10¹¹ NPs/cm², were mainly distributed on the top layer of porous TiO₂ films. The deposition of Au NPs induced a negative shift (~ 100 mV) of the apparent flat band potential of Au-TiO₂ electrodes. The charge separation efficiency of the TiO₂ electrode increased from 72.1% to 88.5% by dispersing Au NPs. Whatever redox species were present in the electrolyte, the Au-TiO₂ electrode had higher photovoltage than the TiO₂ electrode. The photovoltage was very sensitive to added redox species such as O₂, O₃, and methanol, and the effect of adsorbed redox species on electron accumulation was discussed. The electrochemical impedance spectroscopic measurements revealed that the charge transfer resistance (R_ct) of Au-TiO₂ films was reduced to 16% of bare TiO₂ electrode, and the decreased R_ct corresponded to the increased photocatalytic activity of Au-TiO₂ films. The beneficial role of uniformly dispersed small Au NPs on the charge separation was discussed. By modifying TiO₂ films with small Au NPs, the photocatalytic activity of TiO₂ films for formaldehyde degradation increased about 2.5 times.     

Machinable Al2O3/BN composite ceramics with strong mechanical properties

Al₂O₃/BN composite ceramics with nano-sized BN dispersions ranging from 0 to 30 vol.% were successfully fabricated by hot-pressing α-Al₂O₃ powders with turbostratic BN (t-BN) coating, which was prepared through chemical processes using boric acid and urea. SEM observations revealed that the nano-sized hexagonal BN (h-BN) particulates were homogeneously dispersed within Al₂O₃ grains as well as at grain boundaries. Vickers hardness of materials decreased with an increase in BN content. The fracture toughness was improved but the fracture strength had a small decrease, in comparison to Al₂O₃ monolithic ceramics. The nanocomposite ceramics with BN content more than 20 vol.% exhibited excellent machinability, which could be drilled using conventional hard metal alloy drills. Drilling rates and normal forces demonstrate the ease of machining of these materials. The preliminary information on the relationship between microstructures and properties are provided. The mechanism of material removal is also discussed.     

Sol-gel preparation of near-infrared broadband emitting Er-doped SiO2-Ta2O5 nanocomposite films

This article reports a study on the preparation, densification process, and structural and optical properties of SiO₂-Ta₂O₅ nanocomposite films obtained by the sol-gel process. The films were doped with Er³⁺, and the Si:Ta molar ratio was 90:10. Values of refractive index, thickness and vibrational modes in terms of the number of layers and thermal annealing time are described for the films. The densification process is accompanied by OH group elimination, increase in the refractive index, and changes in film thickness. Full densification of the film is acquired after 90 min of annealing at 900 °C. The onset of crystallization and devitrification, with the growth of Ta₂O₅ nanocrystals occurs with film densification, evidenced by high-resolution transmission electron microscopy. The Er³⁺-doped nanocomposite annealed at 900 °C consists of Ta₂O₅ nanoparticles, with sizes around 2 nm, dispersed in the SiO₂ amorphous phase. The main emission peak of the film is detected at around 1532 nm, which can be assigned to the ⁴I_13/2 → ⁴I_15/2 transition of the Er³⁺ ions present in the nanocomposites. This band has a full width at half medium of 64 nm, and the lifetime measured for the ⁴I_13/2 levels is 5.4 ms, which is broader compared to those of other silicate systems. In conclusion, the films obtained in this work are excellent candidates for use as active planar waveguide.     

Rapid synthesis, characterization and optical properties of TiO2 coated ZnO nanocomposite particles by a novel microwave irradiation method

A novel and rapid microwave method was used to prepare TiO₂ coated ZnO nanocomposite particles. The resulted particles were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), high resolution transmission electron microscopy (HR-TEM) and X-ray photoelectron spectroscopy (XPS). Results show that ZnO nanoparticles were coated with 6-10 nm amorphous TiO₂ layers. In addition, zeta potential analysis demonstrated the presence of TiO₂ layer on the surface of ZnO nanoparticles. Photoluminescence (PL) spectroscopy and UV-visible spectroscopy were used to investigate the optical properties of the nanoparticles. Compared to uncoated ZnO nanoparticles, the TiO₂ coated ZnO nanoparticles showed enhanced UV emission. The UV-visible diffuse reflectance study revealed the significant UV shielding characteristics of the nanocomposite particles. Moreover, amorphous TiO₂ coating effectively reduced the photocatalytic activity of ZnO nanoparticles as evidenced by the photodegradation of Orange G with uncoated and TiO₂ coated ZnO nanoparticles under UV radiation.     

Charge trapping characteristics of Al2O3/Al-rich Al2O3/SiO2 stacked films fabricated by radio-frequency magnetron co-sputtering

A thin-film structure comprising Al₂O₃/Al-rich Al₂O₃/SiO₂ was fabricated on Si substrate. We used radio-frequency magnetron co-sputtering with Al metal plates set on an Al₂O₃ target to fabricate the Al-rich Al₂O₃ thin film, which is used as a charge storage layer for nonvolatile Al₂O₃ memory. We investigated the charge trapping characteristics of the film. When the applied voltage between the gate and the substrate is increased, the hysteresis window of capacitance-voltage (C-V) characteristics becomes larger, which is caused by the charge trapping in the film. For a fabricated Al-O capacitor structure, we clarified experimentally that the maximum capacitance in the C-V hysteresis agrees well with the series capacitance of insulators and that the minimum capacitance agrees well with the series capacitance of the semiconductor depletion layer and stacked insulator. When the Al content in the Al-rich Al₂O₃ is increased, a large charge trap density is obtained. When the Al content in the Al-O is changed from 40 to 58%, the charge trap density increases from 0 to 18 × 10¹⁸ cm^− 3, which is 2.6 times larger than that of the trap memory using SiN as the charge storage layer. The device structure would be promising for low-cost nonvolatile memory.     

Formation of NiFe2O4 nanoparticles by mechanochemical reaction

Preparation of nanosized NiFe₂O₄ particles by mechanochemical reaction(NiO+α-Fe₂O₃) and subsequent thermal treatment was investigated using X-ray diffraction (XRD). Thermal treatment of the as-milled powder at 700 °C for 1 h led to the formation of NiFe₂O₄ nanoparticles with an average crystal size of about 23 nm. Effect of thermal treatment temperature on the crystal size of the nanoparticles was studied. The mechanism of nanoparticles growth was primarily discussed. The activation energy of NiFe₂O₄ nanoparticle formation during calcination was calculated to be 16.6 kJ/mol.     

Synthesis and characterization of Al2O3 hollow spheres

This paper presents a novel technique to create Al₂O₃ hollow spherical nanoparticles. It used Al(OH)₃ which was synthesized with Al₂(SO₄)₃ and NaOH, and the C-Al(OH)₃ core-shell nanoparticle as intermediate phases. The Al₂O₃ hollow spheres were achieved by the calcination of the carbon cores and the dehydration of Al(OH)₃. The chemical composition, morphology, size and superficial crystal structure of the nanoparticles were characterized with TEM, XRD, TGA, FTIR and BET. The result shows that the average diameter of the C-Al(OH)₃ core-shell nanoparticles is about 25 nm, the thickness of the Al₂O₃ shell is about 5 nm and the surface area is 215.2 m²/g. The procedure for the formation of Al₂O₃ hollow nanoparticles is discussed in details.     

Sintering and dielectric properties of 0.88Al2O3-0.12TiO2 microwave ceramics by glass addition

The microwave characteristics and the microstructures of 0.88Al₂O₃-0.12TiO₂ with various amounts of MgO-CaO-SiO₂-Al₂O₃ (MCAS) glass sintered at different temperatures have been investigated. The sintering temperature can be lowered to 1300 °C by the addition of MCAS glass. The densities, dielectric constants (ε_r) and quality values (Q×f) of the MCAS-added 0.88Al₂O₃-0.12TiO₂ ceramics decrease with the increase of MCAS glass content. The temperature coefficients of the resonant frequency (τ_f) are shifted to more negative values as the MCAS content or the sintering temperatures increase. The change of the crystalline phases of Al₂TiO₅ phase and rutile-TiO₂ phase has profound effects on the microwave dielectric properties of the MCAS-added Al₂O₃-TiO₂ ceramics. As sintered at 1250 °C, 0.88Al₂O₃-0.12TiO₂ ceramics with 2 wt.% MCAS glass addition exists a ε_r value of 8.63, a Q×f value of 9578 and a τ_f value of +5 ppm/°C.     

On structure and mechanical properties of ultrasonically cast Al-2% Al2O3 nanocomposite

An investigation on the structure of an ultrasonically cast nanocomposite of Al with 2 wt.% nano-sized Al₂O₃ (average size ∼10 nm) dispersoids showed that the nanocomposite was consisting of nearly continuous nano-alumina dispersed zones (NDZs) in the vicinity of the grain boundaries encapsulating Al₂O₃ depleted zones (ADZs). The mechanical properties were investigated by nanoindentation and tensile tests. The nano-sized dispersoids caused a marginal increase in the elastic modulus, and a significant increase in the hardness (∼92%), and tensile strength (∼48%). Subsequent cold rolling to achieve a reduction ratio of 2 resulted in an appreciable increase in the hardness due to change in morphology of the microstructure. Estimation of the strength on the basis of inter-particle spacing, which was measured by transmission electron microscopy, could not be accounted for on the basis of Orowan mechanism, and therefore, strengthening mechanisms like local climb and/or cross slip might have a role in this room temperature (0.32T_M) deformation process.     

Mechanical properties and microstructure of Al2O3/TiAl in situ composites doped with Cr2O3

Al₂O₃/TiAl composites were successfully fabricated from powder mixtures of Ti, Al, TiO₂ and Cr₂O₃ by a hot-press-assisted exothermic dispersion method. The effect of the Cr₂O₃ addition on the microstructures and mechanical properties of Al₂O₃/TiAl composites was characterized, and the results showed that the Rockwell hardness, flexural strength and fracture toughness of the composites increased as the Cr₂O₃ content increased. When the Cr₂O₃ content was 2.5 wt%, the flexural strength and the fracture toughness attained peak values of 925 MPa and 8.55 MPa m^1/2, respectively. This improvement of mechanical properties was due to the more homogeneous and finer microstructure developed from the addition of Cr₂O₃ and an increase in the ratio of α₂-Ti₃Al to γ-TiAl matrix phases.     

NH4Cl-assisted low temperature synthesis of anatase TiO2 nanostructures from Ti powder

A simple, low temperature and low cost method, which was based on heating the mixture of Ti and NH₄Cl powders in air at 300 °C, has been developed for the controlled synthesis of anatase TiO₂ nanostructures including irregular nanoparticle aggregates, curved nanowires built up by the oriented attachment of nanoparticles, and nanoplates constructed with nanoparticles. The characterization results from X-ray diffraction and Raman spectra indicated that the as-obtained products were anatase TiO₂. Field emission scanning electron microscope images revealed that the products obtained for 3, 10 and 16 h comprised, in turn, irregular nanoparticle aggregates (8-55 nm), curved nanowires built up by the oriented attachment of nanoparticles (~ 9 nm), and nanoplates constructed with nanoparticles (~ 8 nm).     

Effect of liquid-forming additives on the sintering and mechanical properties of Al2O3/3Y-TZP (30 vol.%) composite

Al₂O₃/3Y-TZP (30 vol.%) composite was pressurelessly sintered with addition of TiO₂MnO₂ and/or CaOAl₂O₃SiO₂ glass. It was found that TiO₂MnO₂ addition greatly enhanced the densification of the composite by the formation of a low-viscosity liquid at sintering temperature. In contrast, the high-viscosity liquid formed by CaOAl₂O₃SiO₂ glass improved mechanical properties because of its repressing effect on grain growth. The composite could be obtained at a temperature as low as 1400°C by co-doping with TiO₂MnO₂ and CAS glass. Bending strength of 552±64 MPa and fracture toughness of 6.03±0.22 MPa m^1/2 were obtained with a doping level of 2 wt.% TiO₂MnO₂ and 2 wt.% CAS glass.     

In situ Al3Ti and Al2O3 nanoparticles reinforced Al composites produced by friction stir processing in an Al-TiO2 system

Al and TiO₂ powders were selected to fabricate in situ Al composites via multiple pass friction stir processing (FSP) based on the thermodynamic analysis. The microstructural investigations indicated FSP would induce reaction between Al and TiO₂. Al₃Ti and Al₂O₃ particles were formed after 4 pass FSP with 100% overlapping. The in situ particles were about 80 nm in size at various FSP conditions, and ultrafine matrix grains 602 nm in size were obtained when water cooling was applied during FSP. Tensile tests indicated that the in situ nanocomposites exhibited pronounced work hardening behavior and a good combination of strength and ductility.     

Photocatalytic hydrogen production over Na2Ti2O4(OH)2 nanotube sensitized by CdS nanoparticles

Na₂Ti₂O₄(OH)₂ nanotubes were obtained by hydrothermal reaction of TiO₂ with concentrated NaOH solution. CdS nanoparticles were then decorated on Na₂Ti₂O₄(OH)₂ nanotubes through partial ion-exchange method. The composite photocatalysts were characterized by X-ray diffraction (XRD), ultraviolet-visible spectra (UV-vis), transmission electron microscope (TEM), etc. The results showed that CdS nanoparticles of 5-6 nm were anchored on the surface of the Na₂Ti₂O₄(OH)₂ nanotubes. Under irradiation of visible light (λ ≥ 430 nm), the prepared CdS/Na₂Ti₂O₄(OH)₂ showed high photoactivity for hydrogen production.     

Improvement compressive strength of concrete in different curing media by Al2O3 nanoparticles

In the present work, the effect of curing medium on microstructure together with physical, mechanical and thermal properties of concrete containing Al₂O₃ nanoparticles has been investigated. Portland cement was partially replaced by Al₂O₃ nanoparticles with the average particle size of 15 nm and the specimens were cured in water and saturated limewater for specific ages. The results indicate that Al₂O₃ nanoparticles up to maximum of 2.0% produces concrete with improved compressive strength and setting time when the specimens cured in saturated limewater. The optimum level of replacement for cured specimens in water is 1.0 wt%. Although the limewater reduces the strength of concrete without nanoparticles when it is compared with the specimens cured in water, curing the specimens bearing nanoparticles in saturated limewater results in more strengthening gel formation around Al₂O₃ nanoparticles causes more rapid setting time together with high strength. Accelerated peak appearance in conduction calorimetry tests, more weight loss in thermogravimetric analysis and more rapid appearance of peaks related to hydrated products in X-ray diffraction results, all indicate that Al₂O₃ nanoparticles could improve mechanical and physical properties of the specimens.