Tribological and Thermo-Mechanical Properties of TiO2 Nanodot-Decorated Ti3C2/Epoxy Nanocomposites

The micromorphology of fillers plays an important role in tribological and mechanical properties of polymer matrices. In this work, a TiO₂-decorated Ti₂C₃ (TiO₂/Ti₃C₂) composite particle with unique micro-nano morphology was engineered to improve the tribological and thermo-mechanical properties of epoxy resin. The TiO₂/Ti₃C₂ were synthesized by hydrothermal growth of TiO₂ nanodots onto the surface of accordion-like Ti₃C₂ microparticles, and three different decoration degrees (low, medium, high density) of TiO₂/Ti₃C₂ were prepared by regulating the concentration of TiO₂ precursor solution. Tribological test results indicated that the incorporation of TiO₂/Ti₃C₂ can effectively improve the wear rate of epoxy resin. Among them, the medium density TiO₂/Ti₃C₂/epoxy nanocomposites gained a minimum wear rate. This may be ascribed by the moderate TiO₂ nanodot protuberances on the Ti₃C₂ surface induced a strong mechanical interlock effect between medium-density TiO₂/Ti₃C₂ and the epoxy matrix, which can bear a higher normal shear stress during sliding friction. The morphologies of worn surfaces and wear debris revealed that the wear form was gradually transformed from fatigue wear in neat epoxy to abrasive wear in TiO₂/Ti₃C₂/epoxy nanocomposites. Moreover, the results of thermo-mechanical property indicated that incorporation of TiO₂/Ti₃C₂ also effectively improved the storage modulus and glass transition temperature of epoxy resin.     

Photocatalytic Degradation of 4,4′-Isopropylidenebis(2,6-dibromophenol) on Sulfur-Doped Nano TiO2

In present work, we examine the photocatalytic properties of S-doped TiO₂ (S1, S2) compared to bare TiO₂ (S0) in present work. The photocatalytic tests were performed in alkaline aqueous solutions (pH = 10) of three differently substituted phenols (phenol (I), 4,4′-isopropylidenebisphenol (II), and 4,4′-isopropylidenebis(2,6-dibromophenol) (III)). The activity of the catalysts was evaluated by monitoring I, II, III degradation in the reaction mixture. The physicochemical properties (particle size, ζ-potential, E_bg, Eu, E⁰_cb, E⁰_vb, σ_o, K_L) of the catalysts were established, and we demonstrated their influence on degradation reaction kinetics. Substrate degradation rates are consistent with first-order kinetics. The apparent conversion constants of the tested compounds (k_app) in all cases reveal the sulfur-loaded catalyst S2 to show the best photocatalytic activity (for compound I and II S1 and S2 are similarly effective). The different efficiency of photocatalytic degradation I, II and III can be explained by the interactions between the catalyst and the substrate solution. The presence of bromine substituents in the benzene ring additionally allows reduction reactions. The yield of bromide ion release in the degradation reaction III corresponds to the Langmuir constant. The mixed oxidation-reduction degradation mechanism results in higher degradation efficiency. In general, the presence of sulfur atoms in the catalyst network improves the degradation efficiency, but too much sulfur is not desired for the reduction pathway.     

Effect of Nanoparticles Surface Bonding and Aspect Ratio on Mechanical Properties of Highly Cross-Linked Epoxy Nanocomposites: Mesoscopic Simulations

The paper aims to study the mechanical properties of epoxy resin filled with clay nanoparticles (NPs), depending on their shapes and content on the surface of a modifying agent capable of forming covalent bonds with a polymer. The cylindrical clay nanoparticles with equal volume and different aspects ratios (disks, barrel, and stick) are addressed. The NPs’ bonding ratio with the polymer (RGC) is determined by the fraction of reactive groups and conversion time and varies from RGC = 0 (non-bonded nanoparticles) to RGC = 0.65 (more than half of the surface groups are linked with the polymer matrix). The performed simulations show the so-called load-bearing chains (LBCs) of chemically cross-linked monomers and modified nanoparticles to determine the mechanical properties of the simulated composites. The introduction of nanoparticles leads to the breaking of such chains, and the chemical cross-linking of NPs with the polymer matrix restores the LBCs and strengthens the composite. At small values of RGC, the largest value of the elastic modulus is found for systems filled with nanoparticles having the smallest surface area, and at high values of RGC, on the contrary, the systems containing disk-shaped particles with the largest surface area have a larger elastic modulus than the others. All calculations are performed within the framework of a mesoscopic model based on accurate mapping of the atomistic structures of the polymer matrix and nanoparticles into coarse-grained representations, which, if necessary, allow reverse data mapping and quantitative assessment of the state of the filled epoxy resin. On the other hand, the obtained data can be used to design the functional materials with specified mechanical properties based on other practically significant polymer matrices and nanofillers.     

Effect of Al2TiO5 Content and Sintering Temperature on the Microstructure and Residual Stress of Al2O3–Al2TiO5 Ceramic Composites

A series of Al₂O₃–Al₂TiO₅ ceramic composites with different Al₂TiO₅ contents (10 and 40 vol.%) fabricated at different sintering temperatures (1450 and 1550 °C) was studied in the present work. The microstructure, crystallite structure, and through-thickness residual stress of these composites were investigated by scanning electron microscopy, X-ray diffraction, time-of-flight neutron diffraction, and Rietveld analysis. Lattice parameter variations and individual peak shifts were analyzed to calculate the mean phase stresses in the Al₂O₃ matrix and Al₂TiO₅ particulates as well as the peak-specific residual stresses for different hkl reflections of each phase. The results showed that the microstructure of the composites was affected by the Al₂TiO₅ content and sintering temperature. Moreover, as the Al₂TiO₅ grain size increased, microcracking occurred, resulting in decreased flexure strength. The sintering temperatures at 1450 and 1550 °C ensured the complete formation of Al₂TiO₅ during the reaction sintering and the subsequent cooling of Al₂O₃–Al₂TiO₅ composites. Some decomposition of AT occurred at the sintering temperature of 1550 °C. The mean phase residual stresses in Al₂TiO₅ particulates are tensile, and those in the Al₂O₃ matrix are compressive, with virtually flat through-thickness residual stress profiles in bulk samples. Owing to the thermal expansion anisotropy in the individual phase, the sign and magnitude of peak-specific residual stress values highly depend on individual hkl reflection. Both mean phase and peak-specific residual stresses were found to be dependent on the Al₂TiO₅ content and sintering temperature of Al₂O₃–Al₂TiO₅ composites, since the different developed microstructures can produce stress-relief microcracks. The present work is beneficial for developing Al₂O₃–Al₂TiO₅ composites with controlled microstructure and residual stress, which are crucial for achieving the desired thermal and mechanical properties.     

Effects of TiO2 Nanoparticle Addition on Microstructure and Selected Properties of Ag–xTiO2 Composites

The paper presents the results of a study of the microstructure and selected properties of silver-based composites reinforced with TiO₂ nanoparticles, produced by the powder metallurgy method. Pure silver powders were mixed with TiO₂ reinforcement (5 and 10 wt%) and 5 mm steel balls (100Cr6) for 270 min in a Turbula T2F mixer to produce a homogeneous mixture. The composites were made in a rigid die with a single-action compaction press under a pressure of 400 MPa and 500 MPa and then sintered under nitrogen atmosphere at 900 °C. Additionally, to improve the density and mechanical properties of the obtained sinters, double pressing and double sintering operations were conducted. As a result, compacts with a density of 90–94% were obtained. The microstructure of the sintered compacts consists of uniform grains, and the TiO₂ reinforcement phase particles are located on the grain boundaries. There were no discontinuities at the Ag–TiO₂ contact boundary, which was confirmed by SEM and TEM analysis. The use of a higher pressure had a positive effect on the hardness and flexural strength of the tested materials. It was found that the composites with 5 wt% TiO₂ pressed under 500 MPa are characterized by the highest level of mechanical properties. The hardness of these composites is 57 HB, while the flexural strength is 163 MPa.     

Peculiarities of the Phase Formation during Electroconsolidation of Al2O3–SiO2–ZrO2 Powders Mixtures

This paper is devoted to the sintering process of Al₂O₃–SiO₂–ZrO₂ ceramics. The studied method was electroconsolidation with directly applied electric current. This method provides substantial improvements to the mechanical properties of the sintered samples compared to the traditional sintering in the air. The research covered elemental and phase analysis of the samples, which revealed phase transition of high-alumina solid solutions into mullite and corundum. Zirconia was represented mainly by tetragonal phase, but monoclinic phase was present, too. Electroconsolidation enabled samples to reach a density of 3.0 g/cm³ at 1300 °C, while the sample prepared by traditional sintering method obtained it only at 1700 °C. For the composite Al₂O₃—20 wt.% SiO₂—10 wt.% ZrO₂ fabricated by electroconsolidation, it was demonstrated that fracture toughness was higher by 20–30%, and hardness was higher by 15–20% compared to that of samples sintered traditionally. Similarly, the samples fabricated by electroconsolidation exhibited elastic modulus E higher by 15–20%. The hypothesis was proposed that the difference in mechanical and physical properties could be attributed to the peculiarities of phase formation processes during electroconsolidation.     

Fabrication of TiO2 – KH550 – PEG Super-Hydrophilic Coating on Glass Surface without UV/Plasma Treatment for Self-Cleaning and Anti-Fogging Applications

In this study, we have developed a self-cleaning transparent coating on a glass substrate by dip coating a TiO₂ – KH550 – PEG mixed solution with super-hydrophilicity and good antifogging properties. The fabrication of the thin-film-coated glass is a one-step solution blending method that is performed by depositing only one layer of modified TiO₂ nanoparticles at room temperature. X-ray diffraction (XRD) and scanning electron microscopy (SEM) were used to determine the structure and morphology of the nanoparticles and the thin-film-coated glass. The surface functional groups were investigated using Fourier-transform infrared spectroscopy (FT-IR), and the optical properties of the glass coating were measured using a UV/Vis spectrometer. The results revealed that the KH-500-modified TiO₂ film coating was in an anatase crystalline form. The hydrophilicity of the coated and uncoated glass substrates was observed by measuring their water contact angle (WCA) using a contact angle instrument. The maximum transparency of the coated glass measured in the visible region (380–780 nm) was approximately 70%, and it possessed excellent super-hydrophilic properties (WCA ~0°) at an annealing temperature of 350 °C without further need of UV or plasma treatment. These results demonstrate the super-hydrophilic coated glass surface has potential for use in self-cleaning and anti-fogging applications.     

Study on Crystallization Process of Li2O–Al2O3–SiO2 Glass-Ceramics Based on In Situ Analysis

In this paper, we used differential scanning calorimetry (DSC), high-temperature X-ray diffraction (HT-XRD), and confocal scanning laser microscopy (CSLM) to investigate the Li₂O–Al₂O_3–SiO₂ glass crystallization process. At 943 K, lithium disilicate (Li₂Si₂O₅) phase crystals began to precipitate in the Li₂O–Al₂O₃–SiO₂ glass with a crystal size of 50–70 nm. At the temperature of 1009 K, petalite (LiAlSi₄O₁₀) crystals began to precipitate in the vitreous phase, forming composite spherical crystals of LiAlSi₄O₁₀ and Li₂Si₂O₅ with size in the range of 90–130 nm. Furthermore, the Kissinger method and KAS method of the JMAK model were used to calculate the crystallization activation energy and the Avrami index “n”. It was found that the precipitation mechanism of the two kinds of crystals is whole crystallization; accordingly, the selection of crystallization heat treatment system was guided to determine the nucleation and crystallization temperature.     

Thermal Annealing Effect on Optical Properties of Binary TiO2-SiO2 Sol-Gel Coatings

TiO₂-SiO₂ binary coatings were deposited by a sol-gel dip-coating method using tetrabutyl titanate and tetraethyl orthosilicate as precursors. The structure and chemical composition of the coatings annealed at different temperatures were analyzed by Raman spectroscopy and Fourier Transform Infrared (FTIR) spectroscopy. The refractive indices of the coatings were calculated from the measured transmittance and reflectance spectra. An increase in refractive index with the high temperature thermal annealing process was observed. The Raman and FTIR results indicate that the refractive index variation is due to changes in the removal of the organic component, phase separation and the crystal structure of the binary coatings.     

Microstructure and Mechanical Properties of TiN–TiB2–hBN Composites Fabricated by Reactive Hot Pressing Using TiN–B Mixture

In this study, TiN–TiB₂–hBN composite ceramics were prepared via reactive hot pressing using TiN and amorphous B powders as raw materials. Different sintering temperatures and composition ratios were studied. The results show that the 70 vol% TiN–17.6 vol% TiB₂–12.4 vol% hBN ceramic composites obtained ideal comprehensive properties at 1600 °C. The relative density, Vickers hardness, bending strength, and fracture toughness were 99%, 11 GPa, 521 MPa, and 4.22 MPa·m^1/2, respectively. Densification was promoted by the highly active reaction product TiB₂, and the structural defects formed in the grains. Meanwhile, the good interfacial bonding between TiN and TiB₂ grains and the uniform dispersion of ultrafine hBN in the matrix contributed to the excellent bending strength. Moreover, the toughening mechanism of crack deflection and grain pull-out improved the fracture toughness.     

Fe–Doped TiO2–Carbonized Medium–Density Fiberboard for Photodegradation of Methylene Blue under Visible Light

Fe–doped titanium dioxide–carbonized medium–density fiberboard (Fe/TiO₂–cMDF) was evaluated for the photodegradation of methylene blue (MB) under a Blue (450 nm) light emitting diode (LED) module (6 W) and commercial LED (450 nm + 570 nm) bulbs (8 W, 12 W). Adsorption under daylight/dark conditions (three cycles each) and photodegradation (five cycles) were separately conducted. Photodegradation under Blue LED followed pseudo-second-order kinetics while photodegradation under commercial LED bulbs followed pseudo-first-order kinetics. Photodegradation rate constants were corrected by subtracting the adsorption rate constant except on the Blue LED experiment due to their difference in kinetics. For 8 W LED, the rate constants remained consistent at ~11.0 × 10⁻³/h. For 12 W LED, the rate constant for the first cycle was found to have the fastest photodegradation performance at 41.4 × 10⁻³/h. After the first cycle, the rate constants for the second to fifth cycle remained consistent at ~28.5 × 10⁻³/h. The energy supplied by Blue LED or commercial LEDs was sufficient for the bandgap energy requirement of Fe/TiO₂–cMDF at 2.60 eV. Consequently, Fe/TiO₂–cMDF was considered as a potential wood-based composite for the continuous treatment of dye wastewater under visible light.     

Closed-Surface Multifunctional Antireflective Coating Made from SiO2 with TiO2 Nanocomposites

An SiO₂-TiO₂ closed-surface antireflective coating was fabricated by the one-dipping method. TiO₂ nanoparticles were mixed with a nanocomposited silica sol, which was composed of acid-catalyzed nanosilica networks and silica hollow nanospheres (HNs). The microstructure of the sol-gel was characterized by transmission electron microscopy. The silica HNs were approximately 40–50 nm in diameter with a shell thickness of approximately 8–10 nm. The branched-chain structure resulting from acidic hydrolysis grew on these silica HNs, and TiO₂ was distributed inside this network. The surface morphology of the coating was measured by field emission scanning electron microscopy and atomic force microscopy. After optimization, transmittance of up to 94.03% was obtained on photovoltaic (PV) glass with a single side coated by this antireflective coating, whose refractive index was around 1.30. The short-circuit current gain of PV module was around 2.14–2.32%, as shown by the current-voltage (IV) curve measurements and external quantum efficiency (EQE) tests. This thin film also exhibited high photocatalytic activity. Due to the lack of voids on its surface, the antireflective coating in this study possessed excellent long-term reliability and robustness in both high-moisture and high-temperature environments. Combined with its self-cleaning function, this antireflective coating has great potential to be implemented in windows and photovoltaic modules.     

Photocatalytic H2 Evolution Using Different Commercial TiO2 Catalysts Deposited with Finely Size-Tailored Au Nanoparticles: Critical Dependence on Au Particle Size

One weight percent of differently sized Au nanoparticles were deposited on two commercially available TiO₂ photocatalysts: Aeroxide P25 and Kronos Vlp7000. The primary objective was to investigate the influence of the noble metal particle size and the deposition method on the photocatalytic activity. The developed synthesis method involves a simple approach for the preparation of finely-tuned Au particles through variation of the concentration of the stabilizing agent. Au was deposited on the TiO₂ surface by photo- or chemical reduction, using trisodium citrate as a size-tailoring agent. The Au-TiO₂ composites were synthetized by in situ reduction or by mixing the titania suspension with a previously prepared gold sol. The H₂ production activities of the samples were studied in aqueous TiO₂ suspensions irradiated with near-UV light in the absence of dissolved O₂, with oxalic acid or methanol as the sacrificial agent. The H₂ evolution rates proved to be strongly dependent on Au particle size: the highest H₂ production rate was achieved when the Au particles measured ~6 nm.     

Influence of Cr3C2 and VC Content on WC Grain Size,WC Shape and Mechanical Properties of WC–6.0 wt. % Co Cemented Carbides

In this paper, the influences of Cr₃C₂/VC content on WC grain size, WC grain shape and mechanical properties of WC–6 wt. % Co cemented carbides were investigated. The results showed that the grain size first rapidly decreased and then slightly decreased with the increasing Cr₃C₂/VC content, and VC led to finer grain size and narrower size distribution. HRTEM/EDS analysis of the WC/Co interface indicates that the segregation concentration of V is much larger than that of Cr, which may be a strong response to the higher inhibition efficiency of VC. The addition of Cr₃C₂ induced triangular prism shape WC grains while VC generated stepped triangular prism grains. Despite the grain growth inhibitor (GGI) mechanisms of Cr₃C₂/VC have been extensively studied in the literature, the doping amount, especially the doping limit, has not been systematically investigated. In this work, the saturated solubilities of Cr and V in cobalt binder phase along with carbon content hare been predicted based on thermodynamic calculations. Based on the theoretical calculations, the doping amount of Cr₃C₂/VC is designed to be gradually increasing until more or less over their maximum solubilities in the binder phase, thereby investigating the subsequent microstructure and mechanical properties. When the doping of Cr₃C₂/VC exceeds the maximum solubility in Co phase, Co-rich Cr-carbides and Co-deficient V-carbides would form respectively, which were detrimental to the transverse rupture strength (TRS) and impact toughness. The hardness increased with the increasing Cr₃C₂/VC content, while the fracture toughness decreased with the increasing Cr₃C₂/VC content. The TRS initially enhanced and then declined, but the stepped triangular prism shape grains and low fraction of WC/Co interface in WC–6Co–VC cemented carbide led to a more pronounced decline in the TRS. The sample with 0.6 wt. % Cr₃C₂ addition had good comprehensive mechanical properties, its hardness, fracture toughness and TRS were 1880 kg/mm², 9.32 MPa·m^1/2 and 3450 MPa, respectively.     

Thermal and Flame Retardant Properties of Phosphate-Functionalized Silica/Epoxy Nanocomposites

We report a flame retardant epoxy nanocomposite reinforced with 9,10-dihydro-9-oxa-10-phosphaphenantrene-10-oxide (DOPO)-tethered SiO₂ (DOPO-t-SiO₂) hybrid nanoparticles (NPs). The DOPO-t-SiO₂ NPs were successfully synthesized through surface treatment of SiO₂ NPs with (3-glycidyloxypropyl)trimethoxysilane (GPTMS), followed by a click reaction between GPTMS on SiO₂ and DOPO. The epoxy nanocomposites with DOPO-t-SiO₂ NPs as multifunctional additive exhibited not only high flexural strength and fracture toughness but also excellent flame retardant properties and thermal stability, compared to those of pristine epoxy and epoxy nanocomposites with a single additive of SiO₂ or DOPO, respectively. Our approach allows a facile, yet effective strategy to synthesize a functional hybrid additive for developing flame retardant nanocomposites.     

Elaboration of Alumina-Zirconia Composites: Role of the Zirconia Content on the Microstructure and Mechanical Properties

Alumina-zirconia (AZ) composites are attractive structural materials, which combine the high hardness and Young’s modulus of the alumina matrix with additional toughening effects, due to the zirconia dispersion. In this study, AZ composites containing different amounts of zirconia (in the range 5–20 vol %) were prepared by a wet chemical method, consisting on the surface coating of alumina powders by mixing them with zirconium salt aqueous solutions. After spray-drying, powders were calcined at 600 °C for 1 h. Green bodies were then prepared by two methods: uniaxial pressing of spray-dried granules and slip casting of slurries, obtained by re-dispersing the spray dried granulates. After pressureless sintering at 1500 °C for 1 h, the slip cast samples gave rise to fully dense materials, characterized by a quite homogeneous distribution of ZrO₂ grains in the alumina matrix. The microstructure, phase composition, tetragonal to monoclinic transformation behavior and mechanical properties were investigated and are here discussed as a function of the ZrO₂ content. The material containing 10 vol % ZrO₂ presented a relevant hardness and exhibited the maximum value of K_I0, mainly imputable to the t → m transformation at the crack tip.     

TiO2 Nanosols Applied Directly on Textiles Using Different Purification Treatments

Self-cleaning applications using TiO₂ coatings on various supporting media have been attracting increasing interest in recent years. This work discusses the issue of self-cleaning textile production on an industrial scale. A method for producing self-cleaning textiles starting from a commercial colloidal nanosuspension (nanosol) of TiO₂ is described. Three different treatments were developed for purifying and neutralizing the commercial TiO₂ nanosol: washing by ultrafiltration; purifying with an anion exchange resin; and neutralizing in an aqueous solution of ammonium bicarbonate. The different purified TiO₂ nanosols were characterized in terms of particle size distribution (using dynamic light scattering), electrical conductivity, and ζ potential (using electrophoretic light scattering). The TiO₂-coated textiles’ functional properties were judged on their photodegradation of rhodamine B (RhB), used as a stain model. The photocatalytic performance of the differently treated TiO₂-coated textiles was compared, revealing the advantages of purification with an anion exchange resin. The study demonstrated the feasibility of applying commercial TiO₂ nanosol directly on textile surfaces, overcoming problems of existing methods that limit the industrial scalability of the process.     

Design an Epoxy Coating with TiO2/GO/PANI Nanocomposites for Enhancing Corrosion Resistance of Q235 Carbon Steel

In this work, a ternary TiO₂/Graphene oxide/Polyaniline (TiO₂/GO/PANI) nanocomposite was synthesized by in situ oxidation and use as a filler on epoxy resin (TiO₂/GO/PANI/EP), a bifunctional in situ protective coating has been developed and reinforced the Q235 carbon steel protection against corrosion. The structure and optical properties of the obtained composites are characterized by XRD, FTIR, and UV–vis. Compared to bare TiO₂ and bare Q235, the TiO₂/GO/PANI/EP coating exhibited prominent photoelectrochemical properties, such as the photocurrent density increased 0.06 A/cm² and the corrosion potential shifted from −651 mV to −851 mV, respectively. The results show that the TiO₂/GO/PANI nanocomposite has an extended light absorption range and the effective separation of electron-hole pairs improves the photoelectrochemical performance, and also provides cathodic protection to Q235 steel under dark conditions. The TiO₂/GO/PANI/EP coating can isolate the Q235 steel from the external corrosive environment, and may generally be regarded a useful protective barrier coating to metallic materials. When the TiO₂/GO/PANI composite is dispersed in the EP, the compactness of the coating is improved and the protective barrier effect is enhanced.     

The Reaction Products of the Al–Nb–B2O3–CuO System in an Al 6063 Alloy Melt and Their Influence on the Alloy’s Structure and Characteristics

To meet aero-engine aluminum skirt requirements, an experiment was carried out using Al–Nb–B₂O₃–CuO as the reaction system and a 6063 aluminum alloy melt as the reaction medium for a contact reaction, and 6063 aluminum matrix composites containing in situ particles were prepared with the near-liquid-phase line-casting method after the reaction was completed. The effects of the reactant molar ratio and the preheating temperature on the in situ reaction process and products were explored in order to determine the influence of in situ-reaction-product features on the organization and the qualities of the composites. Thermodynamic calculations, DSC analysis, and experiments revealed that the reaction could continue when the molar ratio of the reactants of Al–Nb–B₂O₃–CuO was 6:1:1:1.5. A kinetic study revealed that the Al thermal reaction in the system produced Al₂O₃ and [B], and the [B] atoms interacted with Nb to generate NbB₂. With increasing temperature, the interaction between the Nb and the AlB₂ produced hexagonal NbB₂ particles with an average longitudinal size of 1 μm and subspherical Al₂O₃ particles with an average longitudinal size of 0.2 μm. The microstructure of the composites was reasonably fine, with an estimated equiaxed crystal size of around 22 μm, a tensile strength of 170 MPa, a yield strength of 135 MPa, an elongation of 13.4%, and a fracture energy of 17.05 × 10⁵ KJ/m³, with a content of 2.3 wt% complex-phase particles. When compared to the matrix alloy without addition, the NbB₂ and Al₂O₃ particles produced by the in situ reaction had a significant refinement effect on the microstructure of the alloy, and the plasticity of the composite in the as-cast state was improved while maintaining higher strength and better overall mechanical properties, allowing for industrial mass production.     

Preparation of TiO2/Black Talc Composite Photocatalyst and the Research on Its Adsorption-Degradation Coupling Effects

In this paper, a TiO₂/black talc composite photocatalyst was prepared by the sol-gel method using TBOT as titanium source and black talc as carrier. Rhodamine B was used as the targeted pollutant to study the adsorption role of carbon in black talc. The results showed that with the adsorption-degradation cycles, the illumination time can be reduced by 40%. The adsorption rate and degradation rate of the composite photocatalyst was also increased. The degradation rate of Rhodamine B reached more than 95%, which fully shows the synergistic effect between TiO₂ nanoparticles and black talc. In this way, the adsorption-degradation coupling of the photocatalyst could be realized.