Effects of mono-dispersed PMMA micro-balls as pore-forming agent on the properties of porous YSZ ceramics

Porous yttria-stabilized zirconia (YSZ) ceramics were successfully fabricated by the dry pressing method with different size (1.8–20 μm) and amount (2–60 vol.%) of mono-dispersed poly methyl methacrylate (PMMA) micro-balls. Different PMMA additions with different size and amount were investigated to achieve optimal thermal and mechanical properties. With increases of the amount of PMMA, the porosity of porous YSZ ceramics ranges from 7.29% to 51.6%, the flexural strength increases firstly and then decreases, and the thermal conductivity decreases continuously. With decreases of the diameter of PMMA micro-balls, the mean pore size and thermal conductivity of porous YSZ ceramics decrease, and the flexural strength of porous YSZ ceramics with same porosity increases firstly and then decreases. The porous YSZ ceramics with a higher porosity (18.44 ± 1.24%), the highest flexural strength (106.88 ± 3.2179 MPa) and low thermal conductivity (1.105 ± 0.15 W/m K) can be obtained when the particle diameter and the amount of PMMA are 5 μm and 20 vol.%, respectively.     

Spark plasma sintering and high-temperature strength of B6O–TaB2 ceramics

Tantalum diboride – boron suboxide ceramic composites were densified by spark plasma sintering at 1900 °C. Strength and fracture toughness of these bulk composites at room temperature were 490 MPa and 4 MPa m^1/2, respectively. Flexural strength of B₆O–TaB₂ ceramics increased up to 800 °C and remained unchanged up to 1600 °C. At 1800 °C a rapid decrease in strength down to 300 MPa was observed and was accompanied by change in fracture mechanisms suggestive of decomposition of boron suboxide grains. Fracture toughness of B₆O–TaB₂ composites showed a minimum at 800 °C, suggestive a relaxation of thermal stresses generated from the mismatch in coefficients of thermal expansion.Flexural strength at elevated temperatures for bulk TaB₂ reference sample was also investigated.Results suggest that formation of composite provides additional strengthening/toughening as in all cases flexural strength and fracture toughness of the B₆O–TaB₂ ceramic composite was higher than that reported for B₆O monoliths.     

Spark plasma sintering of TiC ceramic with tungsten carbide as a sintering additive

By adding a small amount of tungsten carbide (WC) as sintering aids, nearly fully dense TiC ceramics were obtained by spark plasma sintering at 1450–1600 °C. The results show that the densification temperature of TiC ceramic was significantly decreased with the addition of 3.5 wt% WC. Compared with the monolithic TiC, the densification temperature of TiC–3.5 wt% WC is lower by ～150 °C and no deterioration of mechanical properties is observed. The TiC composite sintered at 1600 °C exhibits full density, a Vickers hardness of 28.2 ± 1.2 MPa, a flexural strength of 599.5 ± 34.7 MPa and a fracture toughness of 6.3 ± 1.4 MPa m^1/2.     

Fabrication and characterization of PIP based C/SiC composites having improved mechanical properties using high modulus M40J carbon fiber as reinforcement

PIP based C/SiC composites are fabricated using high modulus M40J carbon fiber. High ceramic yield polycarbosilane (PCS) was also synthesized in the laboratory and the same was used to infiltrate the fibrous preforms. The infiltrated preforms were pyrolyzed at three different temperatures viz. 1400, 1500 and 1600 °C and termed as set-1, set-2 and set-3. Flexural strength was determined using 3-point bend fixture and the data obtained are analyzed using Weibull distribution. Average flexural strengths were found to be 691±23 MPa, 654.6±24 MPa, and 504±31 MPa for the sets 1, 2 and 3 respectively and the corresponding Weibull moduli were found to be 27.9, 25.5 and 15.6. The composites pyrolyzed at 1400 and 1500 °C, have been found to exhibit extensive fiber pull-out and thus demonstrated pseudo-ductile fracture behavior. A relatively brittle fracture was observed for the composites pyrolyzed at 1600 °C. Area under the flexural stress and displacement curve is found to be in the ratio 1.0:0.92:0.8 for the for the sets 1, 2 and 3 respectively. The effect of the pyrolysis temperature on the mechanical properties is discussed in the light of the microstructure of the composites.     

Development of SiC–SiC joint by reaction bonding method using SiC/C tapes as the interlayer

SiC/C tapes with different compositions and thicknesses were used to join pressureless sintered silicon carbide ceramics by reaction bonding method. The microstructure of the joints and the influences of joint thickness and residual silicon content in joint layer on the 4-point flexural strength of as joined SiC ceramics have been investigated. Specimens with high flexural strength can be achieved through the control of the composition and the thickness of the joint layer. The highest flexural strength of the joined specimens with the joint thickness of 13 μm can reach 346 ± 35 MPa and 439 ± 31 MPa at room temperature and 1250 °C, respectively. The microstructure development and the reaction bonding mechanism were also studied.     

Hardened properties of high-performance printing concrete

This paper presents the hardened properties of a high-performance fibre-reinforced fine-aggregate concrete extruded through a 9 mm diameter nozzle to build layer-by-layer structural components in a printing process. The printing process is a digitally controlled additive method capable of manufacturing architectural and structural components without formwork, unlike conventional concrete construction methods. The effects of the layering process on density, compressive strength, flexural strength, tensile bond strength and drying shrinkage are presented together with the implication for mix proportions. A control concrete (mould-cast specimens) had a density of approximately 2250 kg/m³, high strength (107 MPa in compression, 11 MPa in flexure) and 3 MPa in direct tension, together with a relatively low drying shrinkage of 175 μm (cured in water) and 855 μm (cured in a chamber at 20 °C and 60% relative humidity) at 184 days. In contrast well printed concrete had a density of 2350 kg/m³, compressive strength of 75–102 MPa, flexural strength of 6–17 MPa depending on testing direction, and tensile bond strength between layers varying from 2.3 to 0.7 MPa, reducing as the printing time gap between layers increased. The well printed concrete had significantly fewer voids greater than 0.2 mm diameter (1.0%) when compared with the mould-cast control (3.8%), whilst samples of poorly printed material had more voids (4.8%) mainly formed in the interstices between filaments. The additive extrusion process was thus shown to retain the intrinsic high performance of the material.     

Effect of PyC interphase thickness on mechanical and ablation properties of 3D Cf/ZrC–SiC composite

Three-dimensional (3D) C_f/ZrC–SiC composites were successfully prepared by the polymer infiltration and pyrolysis (PIP) process using polycarbosilane (PCS) and a novel ZrC precursor. The effects of PyC interphase of different thicknesses on the mechanical and ablation properties were evaluated. The results indicate that the C_f/ZrC–SiC composites without and with a thin PyC interlayer of 0.15 µm possess much poor flexural strength and fracture toughness. The flexural strength grows with the increase of PyC layer thickness from 0.3 to 1.2 µm. However, the strength starts to decrease with the further increase of the PyC coating thickness to 2.2 µm. The highest flexural strength of 272.3±29.0 MPa and fracture toughness of 10.4±0.7 MPa m^1/2 were achieved for the composites with a 1.2 µm thick PyC coating. Moreover, the use of thicker PyC layer deteriorates the ablation properties of the C_f/ZrC–SiC composites slightly and the ZrO₂ scale acts as an anti-ablation component during the testing.     

High temperature physical and mechanical properties of large-scale Ti2AlC bulk synthesized by self-propagating high temperature combustion synthesis with pseudo hot isostatic pressing

The electrical, thermal, and mechanical properties as well as the effect of the temperature of large-scale Ti₂AlC bulk synthesized by self-propagating high temperature combustion synthesis with pseudo hot isostatic pressing were investigated in detail. With increasing temperature, the lattice defects contribute to the decreasing phonon thermal conductivity, and the electrical resistivity increases linearly from room temperature (RT) to 900 °C. The RT flexural strength, compressive strength, fracture toughness, work of fracture, and Vickers hardness were measured to be 606 ± 20 MPa, 1057 ± 84 MPa, 6.9 ± 0.2 MPa m^1/2, 158 ± 12 J/m², and 4.7 ± 0.2 GPa, respectively. With increasing temperature, the flexural and compressive strengths both keep almost unchanged in the zone of brittle failure, but decrease sharply as the plastic deformation occurs. The brittle-plastic transition temperature under flexure (900–950 °C) is higher than compression (700–800 °C). Interestingly, a non-catastrophic failure is observed in the SENB test, with the high work of fracture (158 ± 12 J/m²).     

Mechanical behavior and ultrasonic non-destructive characterization of elastic properties of cordierite-based ceramics

The structural and morphological evolutions of cordierite-based ceramics produced from stevensite/andalusite mixture sintered from 1150 to 1350 °C were studied using X-ray diffraction (XRD) and scanning electron microscopy (SEM). The mechanical behavior was investigated by three-point bending and Brazilian tests. The elastic properties were evaluated using ultrasonic non-destructive testing (NDT). XRD results revealed that the main crystalline phase formed at 1300 and 1350 °C was cordierite with traces of mullite. A linear-elastic behavior followed by brittle fracture was observed in three-point bending test with the presence of multiple discontinuities. Flexural and diametral compression strength values of cordierite sintered at 1300 °C were 39.4±4 and 21.8±2 MPa, respectively. The elastic properties such as Young's modulus (38.7–45.1 GPa), shear modulus (17.90–19.42 GPa) and Poisson ratio (0.08–1.6) of cordierite-based ceramics produced at 1350 and 1300 °C were also determined.     

Structural study of mullite based ceramics derived from a mica-rich kaolin waste

Mullite-based ceramics have been synthesized by reactive sintering of a mixture containing kaolin and a mica-rich kaolin waste. Samples fired in the temperature range from 1300 to 1500 °C were characterized by X-ray diffraction (XRD). The quantitative phase analysis and unit cell parameters of the mullite were determined by Rietveld refinement analysis of the XRD data. Mullite-based ceramics with 1.2 wt% quartz, 56.3 wt% glass (amorphous phase), 2.64 g/cm³ of apparent density, and 35±1.2 MPa of flexural strength were obtained after firing at 1500 °C. A liquid phase sintering mechanism activated by a total mica content of 13.3 wt% allowed to increase the mullite content to 47.6 wt% (2.3 wt% quartz and 50.1 wt% glass phase) and improve the flexural strength (70±3.9 MPa) after firing at 1400 °C.     

Flexural strength and fracture behavior of ZrB2–SiC ultra-high temperature ceramic composites at 1800 °C

ZrB₂–15 vol.%SiC and ZrB₂–30 vol.%SiC composites with smaller starting particle sizes in which the particle sizes of ZrB₂ and SiC are 2 μm and 0.5 μm, respectively, demonstrated marked plasticity and significant reduction in the flexural strength at 1800 °C. The flexural strengths of these two composites are 112 ± 12 MPa and 48 ± 10 MPa, respectively, and their corresponding strength retentions are 13% and 7%, respectively. Large ZrB₂ grains were commonly observed in the samples containing 15 vol.%SiC, which are always the sites for the crack initiation. Cavities were found in the samples containing 30 vol.%SiC and the grain boundaries are the main sites for the crack and cavity nucleation. To improve ultra-high temperature strength, larger starting particle sizes (ZrB₂ and SiC are 5 μm and 2 μm, respectively) were used for the preparation of ZrB₂–15 vol.%SiC. This sample fractured in an elastic manner up to 1800 °C and showed a very high strength with a value of 217 ± 16 MPa.     

TiN modified SiC with enhanced strength and electrical properties

SiC based composites were manufactured with varying TiN content (0–50 V%) using Al₂O₃ and Y₂O₃ sintering aids. Basic dilatometry measurements were performed to determine when densification begins within the composite system. Samples were consolidated via uni-axial hot pressing at 1900 °C to produce ceramic composites with >98% theoretical density. Electrical measurements show increasing TiN additions reduce resistivity and begin to plateau at 40–50V%. Resistivity decreased from 2.0 × 10⁵ Ω − cm (0% TiN) to 2.0 × 10⁻⁴ Ω − cm (50V% TiN). Flexural strengths were characterized and compared against a baseline (0% TiN) SiC. Strengths increased gradually with TiN content. A maximum strength 921 MPa was observed at 40V% TiN content vs. 616 MPa for the baseline SiC. This was a gain of 50% over baseline. Additions beyond that range did not produce further gains in strength.     

Direct coagulation casting of yttria-stabilized zirconia using magnesium citrate and glycerol diacetate

Direct coagulation casting via controlled release of high valance counter ions (DCC-HVCI) has been reported in recent years. In this paper, concentrated yttria-stabilized zirconia (YSZ) suspensions were coagulated using DCC-HVCI method with magnesium citrate as coagulating agent assisted by pH shift in the presence of glycerol diacetate. The effect of ammonium polyacrylate (PAA-NH₄) on the dispersibility of YSZ powder was investigated. The influence of concentrations of glycerol diacetate and magnesium citrate on pH and viscosities of YSZ suspensions was studied. The results indicate that concentrated YSZ suspensions can be coagulated by adding 2 vol% glycerol diacetate and magnesium citrate above 0.5 wt% at room temperature for 2–5 h. The compressive strength of coagulated wet samples is above 2.0 MPa. YSZ ceramics sintered at 1450 °C show homogeneous microstructures with relative densities of 98.9–99.2%. Flexural strength of YSZ ceramics is 869±84 MPa.     

Microstructure and mechanical properties of hot-pressed B4C/TiC/Mo ceramic composites

Boron carbide (B₄C)/TiC/Mo ceramic composites with different content of TiC were produced by hot pressing. The effect of TiC content on the microstructure and mechanical properties of the composites has been studied. Results showed that chemical reaction took place for this system during hot pressing sintering, and resulted in a B₄C/TiB₂/Mo composite with high density and improved mechanical properties compared to monolithic B₄C ceramic. Densification rates of the B₄C/TiC/Mo composites were found to be affected by additions of TiC. Increasing TiC content led to increase in the densification rates of the composites. The sintering temperature was lowered from 2150 °C for monolithic B₄C to 1950 °C for the B₄C/TiC/Mo composites. The fracture toughness, flexural strength, and hardness of the composites increased with increasing TiC content up to 10 wt.%. The maximum values of fracture toughness, flexural strength, and hardness are 4.3 MPa m^1/2, 695 MPa, and 25.0 GPa, respectively.     

Fabrication and mechanical properties of laminated HfC–SiC/BN ceramics

Laminated HfC–SiC/BN ceramics were successfully fabricated by tape casting and hot pressing. Fully dense HfC–SiC ultra-high temperature ceramics with homogeneous structure were obtained. The introduction of the weak BN layer resulted in a slight decrease of the flexural strength but significantly improved the fracture toughness compared with monolithic HfC–SiC ceramics. The fracture toughness of laminated HfC–SiC/BN ceramics in the parallel direction peaked at 8.06 ± 0.46 MPa m^1/2, which increased by 115% than that of monolithic HfC–SiC ceramics. The composites showed non-catastrophic fracture behaviors in both parallel and perpendicular directions. It indicates that laminated structure design is a promising approach to obtain full density HfC–SiC ceramics with high fracture toughness.     

Effect of particle size on the mechanical properties of reaction bonded boron carbide ceramics

In the present communication, effect of boron carbide particle size on the mechanical properties such as hardness, fracture toughness and flexural strength of reaction bonded boron carbide (RBBC) ceramics were investigated. RBBC composites were produced by the reactive infiltration of molten silicon into porous preform containing boron carbide and free carbon. Boron carbide powders with mean particle size of 18.65 μm, 33.70 μm and 63.35 μm were chosen for the RBBC composites. The experimental results show that hardness increases from 1261.70±64.74 kg/mm² to 1674.90±100.00 kg/mm² and fracture toughness drops from 5.76±0.26 MPa m^1/2 to 3.4±0.37 MPa m^1/2. However, flexural strength decreases from 403.41±5.70 MPa to 256.15±25.05 MPa with the increase in particle size. Indentation induced cracks in RBBC are mainly median type and number of cracks increase with the increase of starting particle size.     

Mechanical properties of ZrB2- and HfB2-based ultra-high temperature ceramics fabricated by spark plasma sintering

Flexural strengths at room temperature, at 1400 °C in air and at room temperature after 1 h oxidation at 1400 °C were determined for ZrB₂- and HfB₂-based ultra-high temperature ceramics (UHTCs). Defects caused by electrical discharge machining (EDM) lowered measured strengths significantly and were used to calculate fracture toughness via a fracture mechanics approach. ZrB₂ with 20 vol.% SiC had room temperature strength of 700 ± 90 MPa, fracture toughness of 6.4 ± 0.6 MPa, Vickers hardness at 9.8 N load of 21.1 ± 0.6 GPa, 1400 °C strength of 400 ± 30 MPa and room temperature strength after 1 h oxidation at 1400 °C of 678 ± 15 MPa with an oxide layer thickness of 45 ± 5 μm. HfB₂ with 20 vol.% SiC showed room temperature strength of 620 ± 50 MPa, fracture toughness of 5.0 ± 0.4 MPa, Vickers hardness at 9.8 N load of 27.0 ± 0.6 GPa, 1400 °C strength of 590 ± 150 MPa and room temperature strength after 1 h oxidation at 1400 °C of 660 ± 25 MPa with an oxide layer thickness of 12 ± 1 μm. 2 wt.% La₂O₃ addition to UHTCs slightly reduced mechanical performance while increasing tolerance to property degradation after oxidation and effectively aided internal stress relaxation during spark plasma sintering (SPS) cooling, as quantified by X-ray diffraction (XRD). Slow crack growth was suggested as the failure mechanism at high temperatures as a consequence of sharp cracks formation during oxidation.     

Mechanical,electrical, and thermal properties of graphene nanosheet/aluminum nitride composites

Graphene nanosheet (GNS)/aluminum nitride (AlN) composites were prepared by hot-pressing and effects of GNSs on their microstructural, mechanical, thermal, and electrical properties were investigated. At 1.49 vol% GNSs content, the fracture toughness (5.09 MPa m^1/2) and flexural strength (441 MPa) of the composite were significantly increased by 30.17% and 17.28%, respectively, compared to monolithic AlN. The electrical conductivity of the composites was effectively enhanced with the addition of GNSs, and showed a typical percolation behavior with a low percolation threshold of 2.50±0.4 vol%. The thermal conductivity of the composites decreased with the addition of GNSs.     

Reliable high strength alumina fabricated by DCC-HVCI using submicron calcium citrate complex

Ceramics with high strength and reliability are highly demanded in engineering applications. In this paper, a modified direct coagulation casting via high valence counter ions (DCC-HVCI) method for alumina using calcium citrate complex assisted by glycerol diacetate was investigated. Calcium citrate complex suspensions were prepared by mixing tri-ammonium citrate and calcium chloride in water. Effect of reaction time on the chelating properties of the prepared suspensions was investigated. Concentrated alumina suspensions with a solid loading of 50 vol% were prepared by mixing the calcium citrate complex suspensions and alumina powder at pH of 10.5. Then the suspensions were coagulated by adding 3–6 vol% glycerol diacetate at temperatures of 40–70 °C for 2–6 h. The compressive strength of the coagulated wet samples is in the range 1.1–2.4 MPa. Alumina ceramics sintered at 1550 °C shows homogeneous microstructures with flexural strength and Weibull modulus of 455±17 MPa and 30, respectively.     

A ceramic–carbon hybrid as a high-temperature structural monolith and reinforcing filler and binder for carbon/carbon composites

A new ceramic–carbon nanostructured hybrid (86 vol.% ceramics, 14 vol.% carbon) formed from organoclay during pyrolysis is reported. It functions as a reinforcing filler and a binder for carbon/carbon (C/C) composites. Alone, it can also serve as a high-temperature structural monolith. During pyrolysis, the ordered montmorillonite clay (d₀₀₁ 31.5 Å) is transformed to mullite, cristobalite and disordered clay, allowing the clay part of the organoclay to serve as both binder and reinforcement. The organic part serves as a binder. Thus, a unidirectional C/C composite (50 vol.% fibers, 33 vol.% carbon matrix, 5 vol.% hybrid and 12% porosity) exhibiting flexural strength 290 MPa, modulus 55 GPa and toughness 2.9 MPa is obtained by 1000 °C 21-MPa hot-press pyrolysis in the presence of mesophase pitch powder, which serves as an additional binder, without densification after the pyrolysis. With the hybrid incorporation, the fiber content decreases from 53 to 50 vol.%, but the flexural strength and modulus are increased by 46% and 14% respectively, relative to the composite without the hybrid but with densification. Hot pressing the organoclay alone forms a black monolithic sheet with high thermal stability, electrical resistivity 6 × 10⁶ Ω cm, flexural strength 180 MPa, modulus 69 GPa, but low ductility.