Fabrication of attractive Li4SiO4 pebbles with modified powders synthesized via surfactant-assisted hydrothermal method

Li₄SiO₄ pebbles have been widely studied as attractive tritium breeding materials in the fusion reactor blanket of international thermonuclear experimental reactor (ITER). In this work, surfactant-assisted hydrothermal method was first employed to prepare ultrafine ceramic powders for fabricating attractive Li₄SiO₄ pebbles. SEM analysis revealed that the introduction of sodium dodecyl sulfate could eliminate the particle aggregation to prepare monodispersed precursor powders, and thus generated the green bodies of pebble with homogeneous microstructure, which was helpful to eventually obtain high-quality Li₄SiO₄ pebbles. Moreover, the effects of sintering temperature on the grain size, relative density, and crush load of Li₄SiO₄ pebbles were also investigated. Li₄SiO₄ pebbles sintered at 700 °C had a high crush load (average value 27.39 N), small grain size (average value 0.57 μm), satisfactory density (88.13%T.D.) and abundant pore structure, which were expected to show favorable tritium release behavior as a promising tritium breeding material for fusion reactor blanket.     

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.     

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.     

One-step fabrication of Li2TiO3 ceramic pebbles using pulsed YAG laser

A large amount of Li-containing ceramic breeder pebbles is packed in the solid breeding blanket of a nuclear fusion reactor. Several pebble fabrication technologies have been proposed in previous studies, including wet process, emulsion method, extrusion spheronization, additive manufacturing, and melt process. However, a simple, energy-effective, and scalable fabrication technology remains to be developed for the automated mass production and reprocessing of used radioactive pebbles post-operation. Selective laser melting potentially enables the quick and automated fabrication of breeder pebbles. Herein, we employ a high-power density pulse laser to produce ceramic breeder pebbles. A pulsed YAG laser was irradiated over a lithium metatitanate (Li₂TiO₃) powder bed in air, and the corresponding temperature was monitored using fiber-type infrared pyrometers. Spherical Li₂TiO₃ pebbles were successfully fabricated in a single step with an average diameter of 0.78 ± 0.13 μm and the sintering density of 87.4% ± 5.6% (input power: 7.9 J/pulse). The irradiated Li₂TiO₃ powder melted and turned spherical under surface tension and rapidly solidified, resulting in uniaxial fine grains and a decrease in the degree of long-range cation ordering.     

Low-cost fabrication of Li2TiO3 tritium breeding ceramic pebbles via low-temperature solid-state precursor method

Lithium metatitanate (Li₂TiO₃) ceramic pebbles were fabricated from the powder synthesised via low-temperature solid-state precursor method. Solid H₂TiO₃ and LiOH·H₂O react chemically during ball milling process to form a nano-sized precursor powder. Pure β-Li₂TiO₃ powder can be obtained by calcining the precursor powder at 500 °C, which is half the temperature of conventional solid-state method. The synthesis process is simple and low-cost, which would be more available to achieve batch production among all feasible techniques. The low-temperature calcination will effectively avoid hard particle aggregates and poor sinterability caused by high-temperature heat treatment, which is conducive to prepare ceramics with good properties. The results show that the powder exhibits high sinterability with small particle size of 19 nm. The Li₂TiO₃ ceramic pebbles sintered at 800 °C have small grain size (470 nm), high relative density (83%) and good crush load (45 N), which has great potential as tritium breeding materials for fusion reactors.     

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.     

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.     

Accurate and uniform fabrication of Li2TiO3 pebbles with high properties based on Stereolithography technology

Li₂TiO₃ is a vital candidate breeder to solve tritium self-consistency of fusion reaction. In this study, Digital Light Processing (DLP) based on Stereolithography technology was used to fabricate Li₂TiO₃ pebbles for the first time. Ceramic suspensions with different solid loadings were prepared by mixing modified Li₂TiO₃ powder with UV-curable premixture. The size error of Li₂TiO₃ green pebbles was corrected by adjusting the deformation factor of equatorial radius, and the Li₂TiO₃ green pebbles were successfully fabricated with an accurate size. After sintering processing, the Li₂TiO₃ pebbles with a uniform diameter of 1.5 mm and better sphericity of 1.01 were yielded. The sintering behavior of Li₂TiO₃ pebbles were investigated. Results showed that the Li₂TiO₃ pebbles formed with 35 vol% solid loading, and sintered at 1050 ℃ had a uniform pore distribution, and also had optimal properties, such as high relative density of 93.6 %TD, and prominent crush load of 92.3 N.     

Effect of fuel-to-oxidizer ratios on combustion mode and microstructure of Li2TiO3 nanoscale powders

A single phase Li₂TiO₃ powder has been fabricated through a facile solution combustion process, using citric acid as the fuel and corresponding nitrates as oxidants. The effect of fuel-to-oxidizer ratio (0.5–1.5) on the combustion process, the phase and microstructure of the products was investigated. By using different combinations of citric acid fuel and metal nitrates, the combustion mode could be controlled. When the fuel-to-oxidizer ratio is 0.75, an eruption combustion mode is realized. Thermodynamic analysis of the combustion reaction shows that as the fuel-to-oxidizer ratio increases, the adiabatic flame temperature during combustion also increases, but the measured maximum temperature decreases. The crystallite size of Li₂TiO₃ powders was calculated to be 18–36 nm at different combustion modes. The as-prepared Li₂TiO₃ powders exhibit excellent sinterability and can be sintered to 90.7% of the theoretical density at 800 °C. The grain size of the Li₂TiO₃ ceramics is around 800 nm.     

Temperature stability and high-Qf of low temperature firing Mg2SiO4–Li2TiO3 microwave dielectric ceramics

In this work, a series of low-temperature-firing (1−x)Mg₂SiO₄–xLi₂TiO₃–8 wt% LiF (x = 35–85 wt%) microwave dielectric ceramics was prepared through conventional solid state reaction. X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) analyses showed that the Li₂TiO₃ phase was transformed into cubic phase LiTiO₂ phase and secondary phase Li₂TiSiO₅. Partial substitution of Mg²⁺ ions for Ti³⁺ ions or Li⁺Ti³⁺ ions increased the cell volume of the LiTiO₂ phase. The dense microstructures were obtained in low Li₂TiO₃ content (x ≤ 65 wt%) samples sintered at 900 °C, whereas the small quantity of pores presented in high Li₂TiO₃ content (x ≥ 75 wt%) samples sintered at 900 °C and low Li₂TiO₃ content (x = 45 wt%) sintered at 850 and 950 °C. Samples at x = 45 wt% under sintering at 900 °C for 4 h showed excellent microwave dielectric properties of ε_r = 10.7, high Q × f = 237,400 GHz and near-zero τ_f = − 3.0 ppm/°C. The ceramic also exhibited excellent chemical compatibility with Ag. Thus, the fabricated material could be a possible candidate for low temperature co-fired ceramic (LTCC) applications.     

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 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.     

Preparation of Li2TiO3 by hydrothermal synthesis and its structure evolution under high energy Ar+ irradiation

Ultrafine lithium titanate (Li₂TiO₃) powder was synthesized by hydrothermal method. The phase formation and transition condition among α, β, and γ-Li₂TiO₃ were discussed. XRD and ICP-AES showed the single α-phase was formed at 180 °C with 2 h hydrothermal reaction, and it transited into β-phase at 400 °C. SEM observation and EDS analysis confirmed the dissolution of TiO₂ and the formation of α-Li₂TiO₃ proceeded simultaneously with preferable growth direction of (-133) lattice. During the phase transition, the powder maintained the small crystallite, which facilitated the fabrication of Li₂TiO₃ bulk with small grain size. After the Ar⁺ irradiation, the surface region to the depth of 3 μm of Li₂TiO₃ ceramic was affected, where the decrease of crystallization and disturbance of short-range order were confirmed by GIXRD and Raman spectroscopy. In spite of the structure change at the surface area, the ceramic bulk maintained the same.     

A novel Li2TiO3–Li2CeO3 ceramic composite with excellent microwave dielectric properties for low-temperature cofired ceramic applications

A novel low-temperature sinterable (1 ? x)Li₂TiO₃-xLi₂CeO₃ (x = 0.08 ? 0.16 in molar) microwave dielectric ceramic was successfully prepared by a conventional solid-state reaction method. The X-ray diffraction and scanning electron microscopy analysis revealed the coexistence of two phases with different structures owing to their good chemical stability. Their relative content was easily adjusted to achieve near-zero temperature coefficient of the resonant frequency (τ_f) according to the mixing rule of dielectrics. The low-temperature sintering and desirable microwave dielectric properties can be simultaneously achieved by adding Li₂CeO₃ to the Li₂TiO₃ matrix owing to its low-firing characteristic and opposite-sign τ_f. The composite ceramics with x = 0.14 could be well sintered at 850 °C and exhibited excellent microwave dielectric properties of ε_r ～ 21.2, Qxf～ 59,039 GHz and τ_f ～?7.4 ppm/°C. In addition, no chemical reaction was identified between the matrix phase and Ag, suggesting that the Li₂TiO₃-Li₂CeO₃ ceramics might be promising candidates for low-temperature co-fired ceramic applications.     

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.     

Low-temperature sintered Bi0.5Na0.5TiO3-SrTiO3 incipient piezoceramics and the co-fired multilayer piezoactuator thereof

Lead-free Bi_0.5Na_0.5TiO₃-SrTiO₃ incipient piezoceramics with Li₂CO₃ and MnO₂ additives were successfully fabricated at low firing temperature for applications in co-fired multilayer piezoactuators. The addition of Li₂CO₃ effectively shifted the sintering temperature from 1230 °C down to 1075 °C, where the ceramics were co-fired with a Ag/Pd (75/25) inner electrode. The prototype actuators were prepared by tape-casting method using ceramics with the composition of 0.74Bi_0.5Na_0.5TiO₃-0.26 SrTiO₃ + 0.15 wt%MnO₂ + 0.45 wt%Li₂CO₃. The total number of active layers was 13, and each ceramic layer had a thickness of 60 μm. The actuator output a large strain up to ∼0.20% at a driving field of 4 kV/mm, due to the field-induced phase transition between the ergodic relaxor and ferroelectric phases. The excellent voltage-displacement performance of the prototype actuator demonstrates the potential for industrial applications.     

Microwave dielectric properties of CaWO4–Li2TiO3 ceramics added with LBSCA glass for LTCC applications

In this work, 0.86CaWO₄–0.14Li₂TiO₃ ceramics were prepared via a traditional solid-state process. The effects of Li₂O–B₂O₃–SiO₂–CaO–Al₂O₃ (LBSCA) addition on the phase formation, sintering character, microstructure and microwave dielectric properties of the ceramics were investigated. A small amount of LBSCA addition could effectively lower the sintering temperature of the ceramics. X-ray diffraction analysis revealed that CaWO₄ and Li₂TiO₃ phases coexisted without producing any other crystal phases in the sintered ceramics. The dielectric constant and Qf values were related to the amount of LBSCA addition and sintering temperatures. All specimens could obtain near-zero temperature coefficient (τ_f) values through the compensation of the positive τ_f of Li₂TiO₃ and the negative τ_f of CaWO₄. The 0.86CaWO₄–0.14Li₂TiO₃ ceramic with 0.5 wt% LBSCA addition and sintered at 900 °C for 3 h exhibited excellent microwave dielectric properties of ε_r=12.43, Qf=76,000 GHz and τ_f=−2.9 ppm/°C.     

Parallel preparation and properties investigation on Li2O-Nb2O5-TiO2 microwave dielectric ceramics

A parallel preparation method was developed using dry powders as starting materials to synthesize multi-compositional microwave dielectric ceramics. The Li₂O-Nb₂O₅-TiO₂ ternary system was investigated as a model material. The validity of the parallel ceramic preparation process was confirmed by synthesizing a group of LiNb_0.6Ti_0.5O₃ ceramics in parallel, which showed the same crystalline structure and close dielectric properties. The ceramic libraries with M-phase-rich samples and Li₂TiO₃-rich samples were prepared using the parallel process, and the microwave dielectric properties and crystal phases were investigated systematically. An excellent microwave ceramic with a composition of 0.55Li₂O-0.05Nb₂O₅-0.40TiO₂ was obtained, which has a dielectric constant of 18.4 and a high quality value (Q × f) of 79000 GHz. This parallel process can be applied extensively to explore a variety of bulk ceramic libraries for discovering new functional materials with high performances.     

A novel low-firing microwave dielectric ceramic Li2ZnGe3O8 with cubic spinel structure

A Li₂ZnGe₃O₈ ceramic was investigated as a promising microwave dielectric material for low-temperature co-fired ceramics applications. Li₂ZnGe₃O₈ ceramic was prepared via the conventional solid-state method. X-ray diffraction data shows that Li₂ZnGe₃O₈ ceramic crystallized into a cubic spinel structure with a space group of P4₁32. Dense ceramic with a relative densities of 96.3% were obtained when sintered at 945 °C for 4 h and exhibited the optimum microwave properties with a relative permittivity (ε_r) of 10.3, a quality factor (Q × f) of 47,400 GHz (at 13.3 GHz), and a temperature coefficient of resonance frequency (τ_f) of −63.9 ppm/°C. The large negative τ_f of Li₂ZnGe₃O₈ ceramic could be compensated by rutile TiO₂, and 0.9Li₂ZnGe₃O₈–0.1TiO₂0·1TiO₂ ceramic sintered at 950 °C for 4 h exhibited improved microwave dielectric properties with a near-zero τ_f of −1.6 ppm/°C along with ε_r of 11.3 and a Q × f of 35,800 GHz (11.6 GHz). Moreover, Li₂ZnGe₃O₈ was found to be chemically compatible with silver electrode when sintered at 945 °C.     

Microstructure and mechanical properties of Al2O3–20 wt%Al2TiO5 composite prepared from alumina and titania nanopowders

In the present work, Al₂O₃–20 wt%Al₂TiO₅ composite was prepared from reaction sintering of alumina and titania nanopowders. The nano-sized raw powders were reconstituted into nanostructured particles by ball milling. Then, the nanostructured reconstituted powders were pressed and pressureless-sintered into bulk ceramics at 1300, 1400, 1500 °C for 2 h. The phase composition and microstructures of reconstituted powders and as-prepared ceramic composites were characterized by using X-ray diffractometer (XRD), scanning electron microscope (SEM), transmission electron microscope and energy-dispersive spectrometer (EDS). The microstructural analysis of the ceramic showed that the average grain size of the alumina–aluminium titanate composite increases with increasing the temperature. Also, SEM proved the existence of a proper interface between Al₂TiO₅ and Al₂O₃ grains and preferential distribution of aluminium titanate particles in the grain boundaries. XRD analysis indicated the absence of rutile titania in the sintered composite ensuring complete formation of aluminium titanate. The hardness of the samples sintered at 1300, 1400, 1500 °C were 4.8, 6.2 and 8.5 GPa, respectively.