Synthesis,characterization and sintering of Li2TiO3 nanoparticles via low temperature solid-state reaction

Synthesis of fine Li₂TiO₃ powders via low-temperature solid-state reaction (LTSSR) was studied. Solid Li₂CO₃ and H₂TiO₃ were blended by planetary ball mill with deionized water as medium. Calcination of the milled powder at low temperature of 500 °C resulted in the formation of pure Li₂TiO₃ nanoparticles. Another Li₂TiO₃ powder was also prepared by the conventional solid-state reaction (SSR) and a good comparison between different routes was realized. The results show that the particle size of LTSSR powder is significantly decreased to 19.6 nm while the one obtained by SSR is 146.6 nm. Low temperature calcined powders have less agglomeration and higher sinterability, which can be sintered at lower temperature. Pebbles sintered from the LTSSR powders at 750 °C exhibit small grain size (650 nm), high relative density (85.1%) and satisfactory crush load (42.8 N), whereas the SSR pebbles can only be sintered above 950 °C with the relative density close to 80%. Besides, the LTSSR samples also have a higher conductivity at room temperature, indicating the lower tritium diffusion barrier in ceramics. It is confirmed that H₂TiO₃ rather than TiO₂ is more appropriate for the solid-state reaction to produce Li₂TiO₃ powders with nano-size particles and favorable properties.     

Preparation and characterization of Li2TiO3 ceramic pebbles by modification of the water-based sol–gel method

Li₂TiO₃ is considered as one of the best candidates for breeding materials. This article adopted a modification water-based sol–gel method to synthesize nano-Li₂TiO₃ powders, which overcomes the poor phase purity, coarse grain, and inferior crushing strength described in the previous literature. In this paper, the thermal effect of the precursor, the crystal phase, and the morphology of the powders were characterized by thermogravimetric analysis/differential thermal analysis (TG/DTA), X-ray diffraction (XRD), and transmission electron microscopy (TEM) techniques. The nano-structured Li₂TiO₃ powders with good dispersion and an average particle size of 20–50 nm were successfully synthesized at 600°C by controlling PH and hydrolysis rate. Moreover, the phase transition temperature for the monoclinic phase β-Li₂TiO₃ was as low as 600°C, which is lower than 750°C using the traditional solid-state method. Meanwhile, the morphology, porosity, crushing load, and thermal conductivity of ceramic pebbles are characterized systematically by using scanning electron microscope (SEM), mercury injection meter, compression strength equipment, and laser scattering method, respectively. Experimental results showed that the Li₂TiO₃ ceramic pebbles with a sphericity of .98, crush load of 48.4 N, and relative density of 90.03 % were successfully prepared at 1050°C for 2 h. This method will provide new guidance for the preparation of tritium breeders.     

An innovative process for synthesis of superfine nanostructured Li2TiO3 tritium breeder ceramic pebbles via TBOT hydrolysis – solvothermal method

In this paper, a method combining hydrolysis of tetrabutyl orthotitanate (TBOT) and solvothermal reaction was first used to fabricate nanostructured Li₂TiO₃ tritium breeder ceramic pebbles. Initially, superfine nanostructured Li₂TiO₃ powders were synthesized with average particle size of about 10?nm, according to TEM. The surface area of precursor particles synthesized via this method was found to be 115.85?m²/g by BET analysis, which is much larger than that of the product obtained using traditional methods. The results showed that precursor particles had high sintering activity. XRD pattern revealed that the phase transition temperature for monoclinic phase Li₂TiO₃ prepared by this method was nearly 450?°C, which was the lowest phase transition temperature reported among all wet chemical methods to date. Subsequently, investigation of ceramic sintering demonstrated that Li₂TiO₃ ceramic pebbles with desired nano-crystalline sizes (27.98 ~ 55.03?nm) were obtained by sintering at 500 ~ 600?°C for 4?h. The possible mechanisms were proposed based on the reaction processes of TBOT hydrolysis, solvothermal reaction and sintering.     

A comparative study on the properties of Li2TiO3 powders and pebbles fabricated by different routes

Lithium titanate (Li₂TiO₃) is one of the promising candidate breeders for tritium self-sufficiency of deuterium(D)-tritium(T) fusion reaction. The differences in powder synthesis methods have a great impact on the properties of Li₂TiO₃ powders and the performance of Li₂TiO₃ ceramic pebbles. In this study, the Li₂TiO₃ powders were successfully synthesized by hydrothermal method and solid-state method, and then the pebbles were fabricated by the agar-based wet method. The mechanism of hydrothermal synthesis of Li₂TiO₃ powder was discussed. For the hydrothermal method, the Li₂TiO₃ powder with single phase can be obtained when the rate of Li/Ti = 2.4, and the powder presented two different morphology, which involved two reaction mechanisms, including in-situ phase transformation mechanism and dissolution-precipitation mechanism, the phase transformation from α-Li₂TiO₃ to β-Li₂TiO₃ accomplished at 400°C, which is lower than that of 750°C for solid-state method. Li₂TiO₃ pebbles prepared by the hydrothermal-wet method had a uniform pore distribution, an optimal grain size of 2.7 μm, a crushing load of 58.6 N, and relative density of 90.2%, respectively. In comparison, pebbles prepared by the solid-state-wet method also had better mechanical properties, which the crushing load and relative density were 53.9 N and 86.9% respectively under the optimal fabrication conditions.     

A two-step heating strategy for low-temperature fabrication of high sinterability and fine MgAlON powder with MgAl2O4 as Mg source

Based on the reaction sequence during synthesis of MgAlON powder by solid-state reaction, a two-step heating strategy is proposed to low-temperature fabricate fine MgAlON powder of high sinterability by using MgAl₂O₄ as Mg source, respectively together with AlON and Al₂O₃+AlN. By introduction of an additional dwelling at 1550 °C to the first heating step, more α-Al₂O₃ dissolve into the solid solution at this temperature. By this way, overlarge particles of Al₂O₃ by agglomeration could be avoided in the next heating step to enable fast full reaction at a lower temperature. By dwelling 30 min at 1550 °C followed by 60 min at 1700 °C, single phase MgAlON powders were successfully prepared by solid-state reaction of all the two batches. The fine MgAlON powder synthesized by MAS+Al₂O₃+AlN batch exhibited high sinterability as the MgAlON ceramics pressureless sintered by this powder at 1880 °C without dwelling showed a transmittance up to 68.3%. The phase assemblage and morphology evolution of the mixture during solid-state reaction were monitored, which verified the effectiveness of the proposed two-step heating strategy. The low synthesis temperature of the two-step heating scheme benefits to prepare pure MgAlON powder with small particle size.     

Fabrication of nanostructured Li2TiO3 ceramic pebbles as tritium breeders using powder particles synthesised via a CTAB-assisted method

Nanostructured Li₂TiO₃ ceramics which may have effective thermal conductivity, excellent tritium release behaviour and good irradiation resistance are regarded as a promising solid tritium breeding material for the fusion reactor blanket of the International Thermonuclear Experimental Reactor (ITER). However, due to the limitations of the preparation technology, reports concerning Li₂TiO₃ nanoceramics have been rare. In this paper, uniform nano-Li₂TiO₃ powder particles which were essential to obtain nanostructured Li₂TiO₃ ceramics pebbles were synthesised via a cetyltrimethylammonium bromide (CTAB)-assisted hydrothermal method, and then rare, homogeneous nanostructured Li₂TiO₃ ceramic pebbles were fabricated with the as-prepared powder particles. The mechanisms by which CTAB can reduce particle agglomeration and be of assistance in achieving a nanostructured Li₂TiO₃ ceramic were also investigated. In addition, systematic experiments on the relationship between the added amount of CTAB and the mechanical properties of the Li₂TiO₃ ceramic structure were also carried out. The results revealed that the desired Li₂TiO₃ nanoceramic could be fabricated when 3% CTAB was introduced, as the Li₂TiO₃ pebbles obtained had a small grain size (90 nm), high relative density (89.71%T.D.) and crush load (99.93 N), which were expected to show favourable potential as a promising tritium breeder material in the fusion reactor blanket.     

Comparison of the microwave and conventional sintering of Li2TiO3 ceramic pebbles

Microwave sintering was employed in the fabrication of Li₂TiO₃ ceramic pebbles using the powders synthesized via hydrothermal method. The as-prepared Li₂TiO₃ powders exhibited high reactivity with an average particle size as small as 40?nm. A comparative study between the microwave and conventional sintering behavior of Li₂TiO₃ pebbles was systematically investigated. The microstructure and density analyses showed that the presence of microwaves accelerated the densification and grain growth, thus decreasing the sintering temperature. Besides, an accelerated phase transformation from α-Li₂TiO₃ to β-Li₂TiO₃ was observed in microwave processing. The Li₂TiO₃ ceramic pebbles obtained by microwave sintering exhibited high density, good mechanical property and uniform microstructure, which might hold good potential as tritium breeding materials for blankets. The results showed that the microwave sintering was a promising process for the fabrication of Li₂TiO₃ pebbles.     

Study on the chemical compatibility between Li2TiO3 ceramic pebbles and diverse advanced structural materials

The tritium breeder and structural materials are necessary components in the blanket to realize tritium (T) self-sustainment of nuclear fusion. The long-term exposure between tritium breeders and structural materials will cause surface corrosion in irradiation environments and then further affect the tritium release behavior. In this study, chemical compatibility between Li₂TiO₃ ceramic pebbles and advanced structural materials was studied systematically at 700 °C for 300 h under He+0.1 % H₂ environment, respectively. The color of the Li₂TiO₃ ceramic pebbles changes from white to dark grey and black. Moreover, the grain size of Li₂TiO₃ ceramic pebbles increases to more than 5 μm, and the crushing load decreased slightly. For the structural materials, the Al-rich oxide layer with about 188.7 nm of 14Cr-5Al oxide dispersion strengthened (ODS) steel and Cr-Fe rich oxide layer with about 1.04 μm of 14Cr-ODS steel were observed on the cross-section. The effective diffusion coefficient of O element in Li₂TiO₃ ceramic moved into ODS steel at 700 °C was calculated to be 3.3 × 10⁻¹⁶cm²/s and 1.02 × 10⁻¹⁴ cm²/s. Unfortunately, when SiC ceramics were contacted with the pebbles, the crystal phase transformed into SiO₂, which severely limits its application. Therefore, these results will provide guidance for the selection of structural materials in the future.     

Fabrication and characterization of Li4SiO4-Li2TiO3 composite ceramic pebbles using extrusion and spherodization technique

The effect of different amount of Li₂TiO₃(LT) (0–15?wt%) addition on the properties of composite Li₄SiO₄ (LS) ceramic pebbles were studied. The Li₄SiO₄-Li₂TiO₃ composite powder was prepared in-situ using solid state method at a calcination temperature as low as 800?°C. The composite pebbles were fabricated using a cost-effective and simple technique called extrusion-spherodization. The sintered pebbles were characterized for density, grain size, pore size distribution, crush load and moisture stability. The density of Li₄SiO₄ composite pebbles was improved for LS-5?wt% LT in comparison to LS pebbles when fired at 1000?°C. Moreover, the LS grain size in the composite pebbles was reduced (5.8?μm) in comparison to LS pebbles. We also found that the average crush load value of the LS-5?wt%LT composite pebbles had been improved by nearly 100% (33?N) to that of the pure LS pebbles (17?N). The LS-5?wt% LT pebbles showed improvement in stability to moisture.     

Preparation of Li2TiO3 ceramic with nano-sized pores by ultrasonic-assisted solution combustion

Li₂TiO₃ is a candidate material for tritium breeding in the future nuclear fusion reactor. In this study, Li₂TiO₃ powder was synthesized by ultrasonic-assisted solution combustion synthesis (USCS) in a single step. The ultrasonic transducer with the power of 1000 W was introduced in the synthesis process. The crystallite size of Li₂TiO₃ powder prepared by utilization of ultrasonic power is significantly decreased to ∼5.0 nm, while the one obtained without ultrasonic power is 20.0 nm. Li₂TiO₃ ceramic sintered from USCS powder at 800 °C exhibits the small grain size of 330 nm and the open pores size of 140 nm. The crush load of the ceramic reaches 37.2 N although the structure is porous. Compared with the ceramic prepared by solid-state reaction and conventional solution combustion synthesis, USCS sample has a higher conductivity of 2.0 × 10⁻⁶ S m⁻¹ at room temperature, indicating the lower tritium diffusion barrier in the ceramic.     

Efficient fabrication of high strength Li2TiO3 ceramic pebbles via improved rolling ball method assisted by sesbania gum binder

In this work, a method combining the spray-drying process and rolling ball method was first selected to mass fabricate Li₂TiO₃ tritium breeder ceramic pebbles. Herein, we overcome the issues namely complex production, high manufacturing cost, and lower mechanical strength in previous reports. The Li₂TiO₃ powder with high packing density after the spray drying process will self-agglomerate to form denser structured pebbles during the rolling ball process assisted by sesbania gum binder solution. The stability of slurry, different binder, binder concentrations, the formation mechanism, and the morphology of green pebbles were investigated by using viscometer, SEM. Moreover, the force on the Li₂TiO₃ green pebbles was also analyzed during the rolling ball process. After the debinding and densification process, the Li₂TiO₃ pebbles have a uniform diameter of 1.2 mm and good sphericity of 0.97. The Micro-CT instrument showed that the internal structure of the Li₂TiO₃ pebbles was dense. The experiment's confirmation shows that the Li₂TiO₃ ceramic pebbles sintered at 1000 °C have optimal mechanical properties such as a crushing load of 108 N and relative density of 92.4%TD, which is much larger than that of the pebbles obtained using traditional methods. This work not only overcomes the core-shell structure but also provides a new platform for better mechanical properties for studying the other materials systems in the future.     

A novel process for fully automatic mass-production of Li2TiO3 ceramic pebbles with uniform structure and size

As an excellent promising tritium breeding material, Li₂TiO₃ ceramic pebbles will be required in large quantities in the future. For this reason, a fully automatic pneumatic eject device based on an improved wet process was employed in the mass-preparation of Li₂TiO₃ ceramic pebbles. The operating principle of the equipment, the preparation process parameters and the performance of the Li₂TiO₃ ceramic pebbles have been studied. The results showed that the spheroidization and solidification process of slurries droplets in the molding medium were critical to the sphericity of pebbles, and the size of the green pebbles was related to the droplet dropping speed、the control pressure and the nozzle inner diameter. It is revealed that more than 90% of the pebbles had an eccentricity of less than 1.1, and the diameter distribution was concentrated between 0.98 mm and 1.03 mm. The Li₂TiO₃ ceramic pebbles with the average grain size of 3.7 μm, the crushing load of 67 N, the relative density of 85.6%, and the porosity of 19.96% can be obtained after sintered at 1100 °C for 2 h. Also, the average pore size was 1.3 μm and the distribution was relatively concentrated. Therefore, this method is expected to meet the future demands of Li₂TiO₃ ceramic pebbles with excellent performance in bulk quantity.     

A novel mass production method for Li2TiO3 tritium breeder ceramic pebbles using polyvinyl alcohol (PVA) and polyvinyl pyrrolidone (PVP) assisted granulation method

A novel mass production method of lithium titanite (Li₂TiO₃) tritium breeder ceramic pebbles using polyvinyl alcohol (PVA) and polyvinyl pyrrolidone (PVP) assisted granulation method (APG) was proposed. A binder solution of polyvinyl alcohol (PVA) was used to modify the Li₂TiO₃ precursor powder. The powders with adhesive properties were prilled to form green pebbles (GPs) by spheronization at a low rotation speed and spraying with polyvinyl pyrrolidone (PVP), in several cycles. Then, the density and the crush load of the GPs were improved by high-speed rolling. Finally, the ceramic pebbles were produced by sintering. The phase, the microstructure, and the crush load of the ceramic pebbles were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and with a universal tester, respectively.     

Mass fabrication of Li2TiO3–Li4SiO4 ceramic pebbles with high strength by facile centrifugal granulation method

The bi-phase Li₂TiO₃–Li₄SiO₄ ceramic pebbles have been considered a promising breeder to realize the tritium self-sustainment in the blanket. However, up to now, the reported ceramic pebbles have the disadvantages of low yield, poor crushing load, and loose internal structure, which cannot meet the practical application requirements. In this work, the Li₂TiO₃–Li₄SiO₄ ceramic pebbles with excellent mechanical properties were fabricated successfully via the centrifugal granulation method with the assistance of introducing a spray-drying process, simulating particle trajectory by discrete element software and improving bonding interface between core and shell with ethylene glycol. The composition, microstructure, and inner structure of the Li₂TiO₃–Li₄SiO₄ ceramic pebbles were investigated, respectively, through X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and X-ray computed tomography (CT). It can be found that the employment of the ethylene glycol solution on the surface of Li₂TiO₃ can make the core and the shell combine well. Moreover, the effect of the rolling speed of the Li₂TiO₃–Li₄SiO₄ ceramic pebbles was investigated via discrete element method (EDEM) simulation and experiments. The experimental results displayed that the Li₂TiO₃–Li₄SiO₄ ceramic pebbles sintered at 1100°C for 2 h have a uniform diameter of 1 mm, a good sphericity of 0.97, and an excellent crushing load of 82.4 N, which are superior to those pebbles that obtained by using the traditional wet methods. Moreover, the CT results showed that the appropriate porosity of the core was 3.21% and of the shell was 10.73%. Therefore, the simple centrifugal granulation method can be applied to prepare the Li₂TiO₃–Li₄SiO₄ ceramic pebbles in a large scale and shed a light to investigate the relevant advanced biphasic tritium breeder materials in the future.     

Flexible TiO2 ceramic fibers near-infrared reflective membrane fabricated by electrospinning

Titanium oxide is a potential high temperature reflective material due to its high melting point, large refractive index, and suitable band gap. The flexible TiO₂ ceramic fibers membrane was successfully fabricated by sol–gel method using the polyacetylacetonetitanium (PAT) as the precursor. In order to obtain high-quality TiO₂ fibers, the PAT precursor with good stability and good spinnability was optimized by adjusting the molar ratio of acetylacetone to Ti to 1:1. The TiO₂ fibers heat-treated at 700?°C had a diameter of 400–500?nm. The crystal phase of TiO₂ fibers was anatase, and the surface of fibers was smooth without obvious defects. In addition, the TiO₂ ceramic fibers membrane heat-treated at 700?°C had good flexibility and tensile strength, and the average reflectance in the wavelength range of 500–2500?nm was up to 91.3%. The fibers membrane exhibits a significant reflection effect in the practical experiments and maintained good morphology of the fibers after 1200?°C test.     

Microwave dielectric properties of MgCo2(VO4)2 ceramics synthesized by a sol–gel method

MgCo₂(VO₄)₂ (MCV) ceramics have been prepared by a sol–gel method as potential candidates for use in microwave applications as a low-temperature co-fired ceramic (LTCC). The sintering and microwave dielectric properties of sol–gel processed MCV were compared with those of solid-state reaction processed MCV. The results showed that sol–gel processed MCV had a higher sinterability due to its much finer particle size. The sol–gel processed MCV was also found to have superior microwave dielectric properties compared with solid-state reaction processed MCV especially at low sintering temperatures.     

Co-precipitation synthesis and sintering of yttrium aluminum garnet (YAG) powders: the effect of precipitant

YAG precursors were co-precipitated from a mixed solution of aluminum and yttrium nitrates using ammonia water and ammonium hydrogen carbonate as precipitants, respectively. Phase evolution of the precursors during calcination and sinterability of the resultant YAG powders were compared between the two methods. The use of ammonia water produced a hydroxide precursor with an approximate composition of Al(OH)₃·0.3[Y₂(OH)₅(NO₃)·3H₂O] which transformed to pure YAG at about 1000°C via YAlO₃ phase. Severe agglomeration caused poor sinterability of the resultant YAG powders. The use of ammonium hydrogen carbonate produced a carbonate precursor with an approximate composition of NH₄AlY_0.6(CO₃)_1.9(OH)₂·0.8H₂O. The precursor directly converted to pure YAG at about 900°C. The precursor was loosely agglomerated and the resultant YAG powders showed good dispersity and excellent sinterability. For the same calcination temperature of 1100°C, YAG powders from the hydroxide precursor and the carbonate precursor densified to ∼81.2 and ∼99.8% of the theoretical, respectively, by vacuum sintering at 1500°C for 2 h.     

Impact of synthesis route on the microstructure and energy-storage properties of (Bi1/2K1/2)TiO3–SrTiO3 relaxor ferroelectric ceramics: Solid-state and hydrothermal approaches

Bismuth potassium titanate (Bi_1/2K_1/2)TiO₃-based relaxor ferroelectrics are promising materials for high-energy-density ceramic capacitors. Herein, we compare the microstructure and energy-storage properties of (Bi_1/2K_1/2)_0.5Sr_0.5TiO₃ (BKST50) ceramics fabricated via two different routes: solid-state and hydrothermal reactions. A BKST50 fine powder composed of well-dispersed cubic nanoparticles was obtained via the hydrothermal reaction, whereas the conventional solid-state reaction resulted in the aggregation of primary particles. The grain size of the ceramics prepared from the hydrothermal powder could be controlled between 273 ± 24 and 936 ± 69 nm while maintaining a relative density of over 95% by simply varying the sintering temperature. On the other hand, ceramics prepared via the solid-state reaction could not be fully densified even at 1200 °C (the highest tested sintering temperature). The hydrothermally derived ceramics withstood higher electric field owing to dense and fine-grained microstructure, leading to a high recoverable energy-storage density of 2.25 J cm⁻³ at 240 kV cm⁻¹.     

Effects of Initial Powder Size on the Densification of Barium Titanate Ceramics Prepared by Microwave‐Assisted Sintering

The effects of initial powder size on microwave‐assisted sintering (MWS) were investigated. BaTiO₃ powders with an average particle size of 50, 100, and 500 nm were prepared and sintered with MWS and conventional heating‐based sintering (CS). Samples of the 50 ‐ and 100‐nm‐sized BaTiO₃ powders were mechanically milled to study the effects of powder crystallinity on microwave absorption during the MWS process. The MWS of the 50‐nm‐sized BaTiO₃ powder resulted in a relative mass density of more than 90% when sintered at 1050°C, whereas the same density was achieved at 1200°C with CS. This difference between the optimal sintering temperatures, which is caused by the absorption of microwaves, was not observed when the 500‐nm‐sized BaTiO₃ powder was used. The sinterability of the BaTiO₃ ceramics prepared through the MWS of mechanically milled, 50‐nm‐sized powders decreased with increasing milling time. However, the sinterability was much higher than that of the BaTiO₃ ceramics prepared through the MWS of the 100‐ and 500‐nm‐sized unmilled powders. In conclusion, microwave absorption has significant effects on the sintering behavior of ~50‐nm‐sized powders, but is negligible for 500‐nm‐sized powders.     

Uniform and fine Mg-γ-AlON powders prepared from MgAl2O4: A promising precursor material for highly-transparent Mg-γ-AlON ceramics

High-purity and sinterability Mg-γ-AlON (Mg_0.1Al_1.53O_1.89N_0.27) powders were synthesized by gas pressure sintering (GPS) of mixed powders of commercial Al₂O₃ and AlN, and lab-made MgAl₂O₄. The Mg-γ-AlON powders exhibited a uniform particle morphology and a small particle size of d₅₀ = 3.4 μm, owing to the use of MgAl₂O₄ as the Mg source. Highly-transparent Mg-γ-AlON ceramics were fabricated using the synthesized Mg-γ-AlON powders by spark plasma sintering (SPS) at 1800 °C for 5 min under an axial pressure of 80 MPa, followed by hot isostatic pressing (HIP) at 1800 °C for 2 h under a nitrogen gas pressure of 190 MPa. The ceramics showed a high in-line transmittance of ～ 80.5% at 450 nm, ascribed to the high sinterability of the MgAl₂O₄ raw powder that leads to a pore-free and fully densified microstructure. This indicates that MgAl₂O₄ as sintering additive is superior over MgO and MgF₂ in the fabrication of Mg-γ-AlON transparent ceramic.