Sulfanilic Acid: A Novel Consolidation Agent for Al2O3 in Aqueous Media

A new solidifying agent, 4-aminobenzene sulfonic acid (sulfanilic acid), is reported in this paper. The consolidation process and mechanism were followed using on viscoelastic, FTIR, SEM, and Hg porosimetry measurements. It was shown that the Al₂O₃ slurries with PAA-Na as dispersant exhibited a high degree of particle stabilization. After the addition of sulfanilic acid, we observed an exponential increase in the storage modulus ( G ') as a function of consolidation time. Correspondingly, Al₂O₃ slurries exhibited a transition from a viscous to an elastic state (in 62 min). FTIR analysis indicated that the consolidation process might follow two steps: first, the adsorption of sulfanilic acid on the Al₂O₃ particle surface; second, the acid–base interaction between the adsorbed PAA-Na molecules and the sulfanilic acid molecules. This interaction could possibly induce the formation of three-dimensional networks through a bridging or charge neutralization mechanism. The as-consolidated Al₂O₃ green samples were homogeneous, with the relative green density being 54.69%. Results showed that it was feasible to introduce sulfanilic acid for the consolidation of Al₂O₃ slurries in aqueous media.     

Optimization of a Nanoparticle Suspension for Freeze Casting

Poly(acrylic acid) (PAA) dispersant concentration, suspension pH, and Al₂O₃ solids loading effects on PAA adsorption onto Al₂O₃ nanoparticles were studied; the stability and rheology of the Al₂O₃ nanoparticle suspensions were examined. The most desirable suspension conditions were 7.5–9.5 for pH and 2.00–2.25 wt% of Al₂O₃ for the PAA concentration. Electrical double-layer thickness and PAA adsorption layer thickness comparison showed that electrosteric stabilization was dominant. 45.0 vol% Al₂O₃ solids loading can be achieved for freeze casting. The maximum solids loading was predicted to be 50.7 vol%. The freeze-cast sample showed that pre-rest before freezing was critical for achieving desirable microstructures.     

Dispersion of SiC in Aqueous Media with Al2O3 and Y2O3 as Sintering Additives

It has been well accepted that polyethylene imine (PEI) is an effective dispersant for silicon carbide (SiC) in aqueous media. However, after the addition of sintering additives (Al₂O₃ and Y₂O₃), this dispersing effect is reduced significantly. In this work, a second dispersant, citric acid, was used to resolve this problem. It was found that citric acid could decrease the slurry viscosity (without sintering additives) and enhance the PEI adsorption on SiC particle surface. The optimal amount of citric acid required to achieve a minimum viscosity for 55 vol% SiC suspensions was equal to ∼0.87 wt% (at pH ∼6.8). With the aid of citric acid, well-stabilized SiC suspensions (containing sintering additives) were realized, which exhibited slight shear thinning rheologies. After tape casting and SPS sintering, dense SiC samples were obtained with a homogeneous fine-crystalline microstructure. Results showed that citric acid was an effective dispersant for improving the dispersion of SiC particles containing sintering additives.     

Effect of Dispersant Concentration on Preparation of an Ultrahigh Density ZnO–Al2O3 Target by Slip Casting

The rheological behavior of concentrated ZnO–Al₂O₃ aqueous suspensions has been studied in order to obtain an ultrahigh-density ZnO–Al₂O₃ composite ceramic target by slip casting. The influence of the mass fraction of polyacrylic acid (PAA) on the fluidity of slurries and the density and strength of the green and sintered bodies was investigated. The slurries exhibited a near-Newtonian flow behavior and had a lower viscosity with 0.3 wt% PAA. The excess of PAA enhanced the green strength and the density and strength of the sintered bodies. An ultrahigh density sintered body (>99.7% theoretical density) could be obtained after pressureless sintering at 1400°C. The Al species were well distributed in the sintered bodies, which showed a homogeneous, defect-free microstructure with no abnormal grain growth.     

Fracture Toughness of Al2O3-Particle-Dispersed Y2O3-Partially Stabilized Zirconia

The fracture toughness of 3 mol% Y₂O₃-ZrO₂ (3Y-PSZ) composites containing 10–30 vol% Al₂O₃ with different particle sizes was investigated. It was found that Al₂O₃ dispersion of up to 30 vol% increased the fracture toughness by 17% to 30%, and the toughness increase was more remarkable in the composite dispersed with Al₂O₃ particles of larger sizes. By combining the effects of the dispersion toughening and phase transformation toughening, the toughness change in the present materials was theoretically predicted, which was in good agreement with the experimental data.     

Processing of Concentrated Aqueous Silicon Nitride Slips by Slip Casting

The optimization of concentrated Si₃N₄ powder aqueous slurry properties to achieve high packing density slipcast compacts and subsequent high sintered densities was investigated. The influence of pH, sintering aid powder (6% Y₂O₃, 4% Al₂O₃), NH₄PA dispersant, and Si₃N₄ oxidative thermal treatment was determined for 32 vol% Si₃N₄ slurries. The results were then utilized to optimize the dispersion properties of 43 vol% solids Si₃N₄-sintering aid slurries. Calcination of the Si₃N₄ powder was observed to result in significantly greater adsorption of NH₄PA dispersant and effectively reduced the viscosity of the 32 vol% slurries. Lower viscosities of the optimized dispersion 43 vol% Si₃N₄-sintering aid slurries resulted in higher slipcast packing density compacts with smaller pore sizes and pore volumes, and corresponding higher sintered densities.     

Synthesis of Porous Si3N4 Ceramics with Rod-Shaped Pore Structure

Porous Si₃N₄ ceramics were synthesized by pressureless sintering of green compacts prepared using slip casting of slurries containing Si₃N₄, 5 wt% Y₂O₃+2 wt% Al₂O₃, and 0–60% organic whiskers composed of phenol–formaldehyde resin with solids loading up to 60 wt%. Rheological properties of slurries were optimized to achieve a high degree of dispersion with a high solid-volume fraction. Samples were heated at 800°C in air and sintered at 1850°C in a N₂ atmosphere. Porosities ranging from 0% to 45% were obtained by the whisker contents (corresponding to 0–60 vol% whisker). Samples exhibited a uniform pore distribution. Their rod-shaped pore morphology originated from burnout of whiskers, and an extremely dense Si₃N₄ matrix.     

Tape Casting of Al2O3/ZrO2 Laminated Composites

Fracture toughness of ZrO₂-toughened alumina could he increased by macroscopic interfaces, such as those existing in laminated composites. In this work, tape casting was used to produce A/A or A/B laminates, where A and B can be Al₂O₃, Al₂O₃/5 vol% ZrO₂, and Al₂O₃/l0 vol% ZrO₂. An increase of toughness is observed, even in the Al₂O₃/Al₂O₃ laminates.     

Alumina Sol-Assisted Sintering of SiC—Al2O3 Composites

The composite sol—gel (CSG) technology has been utilized to process SiC—Al₂O₃ ceramic/ceramic particulate reinforced composites with a high content of SiC (up to 50 vol%). Alumina sol, resulting from hydrolysis of aluminum isopropoxide, has been utilized as a dispersant and sintering additive. Microstructures of the composites (investigated using TEM) show the sol-originating phase present at grain boundaries, in particular at triple junctions, irrespective of the type of grain (i.e., SiC or Al₂O₃). It is hypothesized that the alumina film originating from the alumina sol reacts with SiO₂ film on the surface of SiC grains to form mullite or alumina-rich mullite-glass mixed phase. Effectively, SiC particles interconnect through this phase, facilitating formation of a dense body even at very high SiC content. Comparative sinterability studies were performed on similar SiC—Al₂O₃ compositions free of alumina sol. It appears that in these systems the large fraction of directly contacting SiC—SiC grains prevents full densification of the composite. The microhardness of SiC—Al₂O₃ sol—gel composites has been measured as a function of the content of SiC and sintering temperature. The highest microhardness of 22.9 GPa has been obtained for the composition 50 vol% SiC—50 vol% Al₂O₃, sintered at 1850°C.     

Densification and Mechanical Properties of B4C with Al2O3 as a Sintering Aid

The densification behavior and mechanical properties of B₄C hot-pressed at 2000°C for 1 h with additions of Al₂O₃ up to 10 vol% were investigated. Sinterability was greatly improved by the addition of a small amount of Al₂O₃. The improvement was attributed to the enhanced mobility of elements through the Al₂O₃ near the melting temperature or a reaction product formed at the grain boundaries. As a result of this improvement in the density, mechanical properties, such as hardness, elastic modulus, strength, and fracture toughness, increased remarkably. However, when the amount of Al₂O₃ exceeded 5 vol%, the level of improvement in the mechanical properties, except for fracture toughness, was reduced presumably because of the high thermal mismatch between B₄C and Al₂O₃.     

Electric-Field-Induced Crack Growth Behavior in PZT/Al2O3 Composites

Hard lead zirconate titanate (PZT) and PZT/Al₂O₃ composites were prepared and the alternating-electric-field-induced crack growth behavior of a precrack above the coercive field was evaluated via optical and scanning electron microscopy. The crack extension in the 1.0 vol% Al₂O₃ composite was significantly smaller than that in monolithic PZT and the 0.5 vol% Al₂O₃ composite. Secondary-phase Al₂O₃ dispersoids were found both at grain boundaries and within grains in the composites. A large number of dispersoids were observed at the grain boundaries in the 1.0 vol% Al₂O₃ composite. It appears that the Al₂O₃ dispersoids reinforce the grain boundaries of the PZT matrix as well as act as effective pins against microcrack propagation.     

Activity–Composition Relations in FeCr2O4–FeAl2O4 and MnCr2O4–MnAl2O4 Solid Solutions at 1500° and 1600°C

Activity–composition relations of FeCr₂O₄–FeAl₂O₄ and MnCr₂O₄–MnAl₂O₄ solid solutions were derived from activity–composition relations of Cr₂O₃–Al₂O₃ solid solutions and directions of conjugation lines between coexisting spinel and sesquioxide phases in the systems FeO–Cr₂O₃–Al₂O₃ and MnO–Cr₂O₃–Al₂O₃. Moderate positive deviations from ideality were observed.     

Uniformly Porous Al2O3/LaPO4 and Al2O3/CePO4 Composites with Narrow Pore-Size Distribution

Porous Al₂O₃/20 vol% LaPO₄ and Al₂O₃/20 vol% CePO₄ composites with very narrow pore-size distribution at around 200 nm have been successfully synthesized by reactive sintering at 1100°C for 2 h from RE₂(CO₃)₃· x H₂O (RE = La or Ce), Al(H₂PO₄)₃ and Al₂O₃ with LiF additive. Similar to the previously reported UPC-3Ds (uniformly porous composites with a three-dimensional network structure, e.g. CaZrO₃/MgO system), decomposed gases in the starting materials formed a homogeneous open porous structure with a porosity of ∼40%. X-ray diffraction, ³¹P magic-angle spinning nuclear magnetic resonance, scanning electron microscopy, and mercury porosimetry revealed the structure of the porous composites.     

Hydrolysis and Dispersion Properties of Aqueous Y2Si2O7 Suspensions

The dispersion of aqueous γ-Y₂Si₂O₇ suspensions, which contain only one component but have a complex ion environment, was studied by the introduction of two different polymer dispersants, polyethylenimine (PEI) and polyacrylic acid (PAA). The suspension without any dispersant remains stable in the pH range of 9–11.5 because of electrostatic repulsion, while it is flocculated upon stirring due to the readsorption of hydrolyzed ions on the colloid surface. However, suspensions with 1 dwb% PEI exhibit greater stability in the pH range of 4–11.5. The addition of PEI shifts the isoelectric point (IEP) of the suspensions from pH 5.8 to 10.8. Near the IEP (pH_IEP=10.8), the stability of the suspensions with PEI is dominated by the steric effect. When the pH is decreased to acid direction, the stabilization mechanism is changed from steric hindrance to an electrosteric effect little by little. PAA also has the effect of reducing the hydrolysis speed via a "buffer effect" in the basic pH range, but the lack of adsorption between the highly ionized anionic polymer molecules and the negative colloid particle surfaces shows no positive effect on hydrolysis of colloids and on the stabilization of Y₂Si₂O₇ suspensions.     

Tribological Properties of Polycrystalline Ti3SiC2 and Al2O3-Reinforced Ti3SiC2 Composites

Tribological properties of Ti₃SiC₂ and Al₂O₃-reinforced Ti₃SiC₂ composites (10 and 20 vol% Al₂O₃) were investigated by using an AISI-52100 bearing steel ball dryly sliding on a linear reciprocating athletic specimen. The friction coefficients were found varying only in a range of 0.1 under the applied loads (2.5, 5, and 10 N), and the wear rates of the composites decreased with increasing Al₂O₃ content. The enhanced wear resistance is mainly attributed to the hard Al₂O₃ particles nail the surrounding soft matrix and decentrale the shear stresses under the sliding ball to reduce the wear losses.     

Homogeneous Fabrication of Al2O3–ZrO2–SiC Whisker Composite by Surface-Induced Coating

Al₂O₃–ZrO₂–SiC whisker composites were prepared by surface-induced coating of the precursor for the ZrO₂ phase on the kinetically stable colloid particles of Al₂O₃ and SiC whisker. The fabricated composites were characterized by a uniform spatial distribution of ZrO₂ and SiC whisker phases throughout the Al₂O₃ matrix. The fracture toughness values of the Al₂O₃–15 vol% ZrO₂–20 vol% SiC whisker composites (∼12 MPa.m^1/2) are substantially greater than those of comparable Al₂O₃–SiC whisker composites, indicating that both the toughening resulting from the process zone mechanism and that caused by the reinforced SiC whiskers work simultaneously in hot-pressed composites.     

Homogeneous ZrO2–Al2O3 Composite Prepared by Nano-ZrO2 Particle Multilayer-Coated Al2O3 Particles

ZrO₂–Al₂O₃ nanocomposite particles were synthesized by coating nano-ZrO₂ particles on the surface of Al₂O₃ particles via the layer-by-layer (LBL) method. Polyacrylic acid (PAA) adsorption successfully modified the Al₂O₃ surface charge. Multilayer coating was successfully implemented, which was characterized by ξ potential, particle size. X-ray diffraction patterns showed that the content of ZrO₂ in the final powders could be well controlled by the LBL method. The powders coated with three layers of nano-ZrO₂ particles, which contained about 12 wt% ZrO₂, were compacted by dry press and cold isostatically pressed methods. After sintering the compact at 1450°C for 2 h under atmosphere, a sintered body with a low pore microstructure was obtained. Scanning electron microscopy micrographs of the sintered body indicated that ZrO₂ was well dispersed in the Al₂O₃ matrix.     

Fabrication of Stable Al2O3 Slurries and Dense Green Bodies Using Wet Jet Milling

A wet jet milling process was used as a novel method to prepare Al₂O₃ slurries. The wet jet-milled slurries showed very low viscosity compared with the ball-milled slurries. Moreover, the viscosity of the wet jet-milled slurries was constant for long times, whereas that of the ball-milled slurries increased rapidly with time. Al₂O₃ particles after wet jet milling retained initial surface conditions, although Al₂O₃ particles after ball milling yielded more OH groups on the surface. Casting rate was sensitive to the solid content and preparation method of slurry. The relative density of the green bodies prepared from the wet jet-milled slurries was about 65% or more and was independent of the slurry solid content. On the other hand, the relative density of the green bodies prepared from the ball-milled slurries increased with increasing solid content and was higher than 60% at the solid content of 50% by volume. Linear shrinkage of the sintered bodies prepared from the wet jet-milled slurries was very low and independent of the solid content of the slurry whereas that of the sintered bodies prepared from the ball-milled slurries increased with decreasing solid content.     

Preparation and Microstructure of Multi-Wall Carbon Nanotubes-Toughened Al2O3 Composite

With multi-wall carbon nanotubes (MWNTs) as reinforcement, a 12 vol% MWNTs/alumina (Al₂O₃) ceramic composite was obtained by hot pressing. A fracture toughness of 5.55±0.26 MPa·m^1/2, 1.8 times that of pure Al₂O₃ ceramics, was achieved. Experimental results showed that the enveloping of carbon nanotubes (CNTs) with sodium dodecyl sulfate (SDS) is effective in changing the hydrophobicity of CNTs to hydrophilicity and improving the dispersion of CNTs in aqueous solution. Enveloped with SDS, CNTs can be homogeneously mixed with Al₂O₃ at a microscopic level by heterocoagulation. This mixing method can obviously improve the chemical compatibility between CNTs and Al₂O₃, which is important for enhancement of interfacial strength between them.     

Formation and Transformation of δ-Ta2O5 Solid Solution in the System Ta2O5-Al2O3

In the system Ta₂O₃-Al₂O₅ solid solutions of metastable δ-Ta₂O₅ (hexagonal) are formed up to 50 mol% Al₂O₃ from amorphous materials prepared by the simultaneous hydrolysis of tantalum and aluminum alkoxides. The values of the lattice parameters decrease linearly with increasing Al₂O₃, content. The to β-Ta₂O₅ (orthorhombic, low-temperature form) transformation occurs at ∼950°C. The solid solution containing 50 mol% Al₂O₃ transforms at 1040° to 1100°C to orthorhombic TaAlO₄. Orthorhombic TaAlO₄ contains octahedral TaO₆ groups in the structure.