Fibrous porous ceramics with devisable phenolic resin reinforcing layer

Fibrous porous ceramics with devisable phenolic resin reinforcing layer were fabricated using low cost atmospheric impregnation technology at room temperature. In combination with additional sealing method, phenolic resin reinforcing layer with controllable thickness could be obtained on the surface of fibrous porous ceramics. Typical gradient profile was observed along the thickness direction of impregnation. The effects of the phenolic resin reinforcing layer on mechanical properties and thermal insulation properties were studied. The results revealed that compressive strength increased from 1.70?MPa to 2.61?MPa, tensile strength increased from 0.78?MPa to 0.91?MPa, and flexural strength increased from 9.55?MPa to 10.89?MPa with the phenolic resin layer increasing from 0?mm to 9?mm. Simultaneously, room-temperature thermal conductivity increased from 0.051?W/(m·K) to 0.055?W/(m·K). In addition, the impact resistance of the surface of the material was obviously improved. The contact angel of the surface of the material exceeded 125°, which effectively improved the environmental adaptability.     

SiC纤维增强玻璃陶瓷的结构与高温力学性能研究

通过ＳＥＭ，ＴＥＭ，ＡＥＳ，抗弯及蠕变试验考察了ＳｉＣ纤维增强的玻璃瓷的微观结构及高温力学性能。实验结果表明：除了在复合材料的基质中存在着大量的针状晶体之外，在纤维与基质的界面还存在着８０ｎｍ厚的富碳层。     

化工陶瓷的成型工艺

介绍了化工陶瓷产品成型操作经验及此工艺中造成半成品缺陷的诸因素。     

普通出口陶瓷的现状分析及有关技术问题探讨

分析了中国陶瓷在国际市场上只能处于较低价位的原因，并提出了发展普通出口陶瓷所应采取的对策，尤其对其有关技术问题作了较为详尽的探讨。     

Composition-dependent xBa(Zr0.2Ti0.8)O3-(1-x)(Ba0.7Ca0.3)TiO3 bulk ceramics for high energy storage applications

This work reports the composition dependent microstructure, dielectric, ferroelectric and energy storage properties, and the phase transitions sequence of lead free xBa(Zr_0.2Ti_0.8)O₃-(1-x)(Ba_0.7Ca_0.3)TiO₃ [xBZT-(1-x)BCT] ceramics, with x?=?0.4, 0.5 and 0.6, prepared by solid state reaction method. The XRD and Raman scattering results confirm the coexistence of rhombohedral and tetragonal phases at room temperature (RT). The temperature dependence of Raman scattering spectra, dielectric permittivity and polarization points a first phase transition from ferroelectric rhombohedral phase to ferroelectric tetragonal phase at a temperature (T_R-T) of 40?°C and a second phase transition from ferroelectric tetragonal phase - paraelectric pseudocubic phase at a temperature (T_T-C) of 110?°C. The dielectric analysis suggests that the phase transition at T_T-C is of diffusive type and the BZT-BCT ceramics are a relaxor type ferroelectric materials. The composition induced variation in the temperature dependence of dielectric losses was correlated with full width half maxima (FWHM) of A₁, E(LO) Raman mode. The saturation polarization (P_s) ≈8.3?μC/cm² and coercive fields ≈2.9?kV/cm were found to be optimum at composition x?=?0.6 and is attributed to grain size effect. It is also shown that BZT-BCT ceramics exhibit a fatigue free response up to 10⁵ cycles. The effect of a.c. electric field amplitude and temperature on energy storage density and storage efficiency is also discussed. The presence of high T_T-C (110?°C), a high dielectric constant (ε_r ≈?12,285) with low dielectric loss (0.03), good polarization (P_s ≈?8.3?μC/cm²) and large recoverable energy density (W?=?121?mJ/cm³) with an energy storage efficiency (η) of 70% at an electric field of 25?kV/cm in 0.6BZT-0.4BCT ceramics make them suitable candidates for energy storage capacitor applications.     

LaMgAl11O19 synthesis using non-hydrolytic sol-gel methods

Polycrystalline LaMgAl₁₁O₁₉ (LMA) was prepared by four different non-hydrolytic sol-gel methods. From stable solutions, four powder precursors containing an amorphous and nanocrystalline phase with specific reactivity were obtained. The particle size, morphology, thermal behaviour, and phase composition of the powder precursors were studied using DLS, TEM, DSC/TG and XRD. Bulk ceramic samples containing LMA were prepared at 1200?°C for 16?h and examined in terms of phase purity and microstructure using XRD, SEM, and TEM. Raman spectroscopy of pure LMA was used to study the structure in detail. A mechanism of LMA formation and a relation between powder precursor properties and final phase composition is proposed. These findings may be useful for designing modern technologies for fabrication of LMA for optical or protective coating applications.     

Influence of Cr3+ substitution for Mg2+ on the crystal structure and microwave dielectric properties of CaMg1-xCr2x/3Si2O6 ceramics

The CaMg_1-xCr_2x/3Si₂O₆ (0?≤?x?≤?0.1) microwave dielectric ceramics were synthesized via conventional solid state reaction. In this study, the effects of Cr³⁺ substituting for Mg²⁺ on morphology, crystal structure and microwave dielectric properties of CaMg_1-xCr_2x/3Si₂O₆ ceramics were explored. XRD diffraction patterns exhibited that the CaMg_1-xCr_2x/3Si₂O₆ ceramics possessed the pure phase of CaMgSi₂O₆ when x?≤?0.06 and a small amount of secondary phase Ca₃Cr₂(SiO₄)₃ for 0.08?≤?x?≤?0.1. SEM micrographs revealed that the substitution of Mg²⁺ with Cr³⁺ could decrease the grain size. The apparent density was affected by the concentration of Mg vacancies. The correlation between crystal structure and microwave dielectric properties was investigated through the Rietveld refinement and Raman analysis. The microwave dielectric properties were mainly dependent on relative density, ionic polarizabilities, internal strain ?, disordered structure and MgO₆ octahedron distortions. Finally, CaMg_1-xCr_2x/3Si₂O₆ (x?=?0.02) ceramics sintered at 1270?°C for 3?h exhibited excellent microwave dielectric properties of ε_r?=?8.06, Q?×?f?=?89054?GHz, τ_f?=??44.92182?ppm/ºC.     

Glass powders and reactive silicone binder: Interactions and application to additive manufacturing of bioactive glass-ceramic scaffolds

A novel concept for the additive manufacturing of three-dimensional glass-ceramic scaffolds, to be used for tissue engineering applications, was based on fine glass powders mixed with a reactive binder, in the form of a commercial silicone. The powders consisted of ‘silica-defective glass’ specifically designed to react, upon firing in air, with the amorphous silica yielded by the binder. By silica incorporation, the glass was intended to reach the composition of an already known CaONa₂OB₂O₃SiO₂ system. Silica from the binder provided up to 15 wt% of the total silica. With the same overall formulation, silicone-glass powder mixtures led to nearly the same phase assemblage formed by the reference system, crystallizing into wollastonite (CaSiO₃) and Ca-borate (CaB₂O₄). Samples from silicone-glass powder mixtures exhibited an excellent shape retention after firing, which was later exploited in highly porous reticulated scaffolds, obtained by means of direct ink writing (DIW).     

Coating Y2O3 nano-particles with ZrO2-additive via precipitation method for colloidal processing of highly transparent Y2O3 ceramics

In the present work, transparent Y₂O₃ ceramics were prepared via colloidal processing method using ZrO₂-coated nano-sized Y₂O₃ powders. The chemical precipitation method was adopted for the coating of Y₂O₃ raw powder. The evolution of the coated-ZrO₂ layer upon calcination was studied. The rheological behaviors of the slurries of Y₂O₃ powders coated with different content of ZrO₂-additive were investigated. The pH_IEP of ZrO₂-coated Y₂O₃ powders shows intermediate values between that of raw Y₂O₃ and ZrO₂ powders. As the ZrO₂-coating concentration increased from 0 to 5.0 at%, the magnitude of the negative zeta potential at pH > pH_IEP shows a general trend of increment, whereas it decreased at pH < pH_IEP. The viscosity decreases pronouncedly with the increase of ZrO₂ content from 0.5 at% to 3.0 at%. The suspensions with low viscosity and high stability was achieved for a solid loading of 35.0 vol% using Y₂O₃ powders coated with 5.0 at% ZrO₂. The dispersed suspensions were consolidated by centrifugal casting method and the green bodies shown improved homogeneity. Transparent Y₂O₃ ceramics were fabricated by vacuum sintering at 1800 ℃ for 5 h. Transmittance at wavelength 800 nm (1.0 mm thick) reached 80.8%, close to the theoretical value of Y₂O₃.     

Investigations of TaB2 on oxidation-inhibition property and mechanism of Si-based coatings in aerobic environment with broad temperature region for carbon materials

To investigate the formation mechanism of the dendrites glass-ceramics and the effect of TaB₂ modifier on the oxidation-inhibition ability of Si-based coatings in aerobic environment with broad temperature region for carbon materials, the Si-based coatings modified with different TaB₂ content were fabricated by the liquid phase sintering method. The fabricated coatings and its corresponding composite powders were investigated in dynamic TG aerobic environments up to 1500 ℃. The initial oxidation temperatures of Si-based coatings modified with TaB₂ powders are almost completely suppressed to 800 ℃. With the increase of TaB₂ phase content, the relative oxygen permeability of the Si-based coatings is significantly reduced, which can be interpreted as the generation of liquid boride, silicide and Ta-Si-B-O compound glass ceramics those can improve the stability of the coating. The formation mechanism of the dendrites glass-ceramics was illustrated.