Optimization of bond strength between gold alloy and porcelain through a composite interlayer obtained by powder metallurgy

The purpose of this study was to evaluate the influence of a composite interlayer (at the metal-ceramic interface) on the shear bond strength of a metal-ceramic composite when compared with a conventional porcelain fused to metal (PFM).Several metal-ceramic composites specimens were produced by hot pressing. To identify which was the best composition for the interlayer several composites, with different relations of metal/ceramic volume fraction, were bonded to metal and to ceramic substrates. The bond strength of the composites to substrates was assessed by the means of a shear test performed in a universal test machine (crosshead speed: 0.5 mm/min) until fracture. Some interfaces of fractured specimens as well as undestroyed interface specimens were examined with optical microscope and scanning electron microscope (SEM/EDS).The shear bond strength results for all composites bonded to metal and to ceramic substrates were significantly higher (>150 MPa) than those registered in the upper range of conventional porcelain fused to metal (PFM) techniques (∼80 MPa). The use of a composite interlayer proved to enhance metal/ceramic adhesion in 160%.     

Fabrication of ferrous metallic foams by reduction of ceramic foam precursors

A process has been developed for obtaining closed cell metallic foams using a ceramic foam precursor. In the present study, the major constituent of the ceramic foam precursor was iron oxide (Fe₂O₃), which was mixed with various foaming/setting additives. The mixture set rapidly at room temperature, stabilizing the foam generated by hydrogen release. The oxide foam was then reduced by annealing at 1240^∘C in a non-flammable hydrogen/inert gas mixture to obtain a metallic foam with a relative density of 0.23 ± 0.017, and an average cell diameter of 1.32 ± 0.32 mm. The iron foams were tested in compression and yielded an average compressive strength of 29 ± 7 MPa. The compressive stress-strain curves obtained were typical of cellular metals. The normalized strengths of the metal foams obtained in the present study compare favorably with those of steel foams produced by other techniques.     

Preparation,microstructure and mechanical properties of dense polycrystalline hydroxy apatite

Hydroxy apatite ceramic blocks of varying density have been prepared from a commercial powder. The elastic properties, fracture toughness, strength and sub-critical crack growth of these materials have been investigated. Young's modulus for the nearly fully dense material is 112 GPa while the compressive strength is about 800 MPa. For the same material the strength and fracture toughness under dry conditions are 115 MPa and 1.0 MPa m^1/2, respectively. Substantial slow crack growth was found under these conditions. Under wet conditions the values for strength and fracture toughness drop to about 75% of their “dry” values. In this case very serious slow crack growth is present.     

Interfacial fracture characteristic and crack propagation of thermal barrier coatings under tensile conditions at elevated temperatures

Thermal barrier coatings (TBCs) have been extensively used in aircraft engines for improved durability and performance for more than fifteen years. In this paper, thermal barrier coating system with plasma sprayed zirconia bonded by a MCrAlY layer to SUS304 stainless steel substrate was performed under tensile tests at 1000°C. The crack nucleation, propagation behavior of the ceramic coatings in as received and oxidized conditions were observed by high-performance camera and discussed in detail. The relationship of the transverse crack numbers in the ceramic coating and tensile strain was recorded and used to describe crack propagation mechanism of thermal barrier coatings. It was found that the fracture/spallation locations of air plasma sprayed (APS) thermal barrier coating system mainly located within the ceramic coating close to the bond coat interface by scanning electron microscope (SEM) and energy dispersive X-Ray (EDX). The energy release rate and interface fracture toughness of APS TBCs system were evaluated by the aid of Suo–Hutchinson model. The calculations revealed that the energy release rate and fracture toughness ranged, respectively, from 22.15 J m⁻² to 37.8 J m⁻² and from 0.9 MPa m^1/2 to 1.5 MPa m^1/2. The results agree well with other experimental results.     

Morphology,strength and pre-coating effect in YSZ/Nl bonding

The quality of ceramic-metal bond is strongly influenced by the microstructure of the transition region between the ceramic and the metal. Sandwich-like ceramic-metal-ceramic specimens are fabricated by solid state bonding of 3 mol% yttria doped zirconia ceramic with nickel foils. Time dependence of the shear strength of the bonding assembly is evaluated at 900° C under a bonding pressure of 8.17 MPa. An optimum strength is obtained for the bonding time between 10 and 25 minutes. The shear strength is also measured as the function of the bonding pressure and bonding temperature. The dependence of the processing parameters on the shear strength of the bond assembly is investigated on the basis of the morphological development in the ceramic-metal interface. In addition, the effect of a pre-coated Ni film on the strength of YSZ/Ni bonding is discussed.     

A fracture mechanics approach to ceramo-metal bond evaluation

The incidence of mechanical failure of cast metal/porcelain dental restorations has promoted a study to develop reliable methods of characterizing and improving bond strengths when produced under standard dental laboratory conditions. Single-edge notch beam specimens were prepared by firing porcelain from a single blended frit to either side of a central metal coupon and subjecting these to four-point bending at 20 ± 2° C and 0.5 mm min^–1 crosshead speed. Specimens of three representative dental alloys and an experimental alloy were prepared in two specimen sizes and three notch widths. The fracture toughness (K _Ic) values were independent of notch width and specimen size over the range of these variables examined and good discrimination was obtained. The fracture toughness of all bonds was improved by a commercial hot isostatic pressure cycle. SEM examination of the fractured surfaces suggested that this improvement was due to the reduction in microporosity at the interface.     

Influence of nano-ZrO2 additive on the bending strength and fracture toughness of fluoro-silicic mica glass–ceramics

Fluoro-silicic mica glass–ceramics were prepared by a sintering process and different proportions of nano-ZrO₂ particles (3Y-TZP) were integrated during the process. Bending strength and fracture toughness were evaluated using a three-point bending test and a Vickers indenter, respectively. The bending strength and fracture toughness improved in significantly with the increase in the quantity of nano-ZrO₂ additives. The highest bending strength of 324.3 ± 12.3 MPa and fracture toughness of 4.2 ± 0.11 MPa m^1/2 were obtained with 30% (wt.) nano-ZrO₂. Good results were also obtained in morphological observations. The glass–ceramic is homogenous and the ZrO₂ grains embed in the lamellar structures of the fluoro-silicic mica homogenously and completely and array well and compactly. On the fracture surface, both the transgranular fracture and the intergranular fracture can be observed clearly.     

Brazing parameters determine the degradation and mechanical behaviour of alumina/titanium brazed joints

The main aims of the present study are simultaneously to relate the brazing parameters with the correspondent interfacial microstructure, the resultant mechanical properties and the electrochemical degradation behaviour of commercially pure titanium/alumina brazed joints. A filler metal on the Ag-26.5Cu-3Ti system has been used. Three different brazing temperatures (850, 900 and 950°C) and three holding times (0.3, 1.2, 2.4 ks) were tested, in order to understand the influence of each combination of brazing temperature holding times, over the final microstructure and properties of the joints. The mechanical properties of the M/C joints were assessed on the basis of bond strength tests carried out using a shear solicitation scheme. The fracture surfaces were studied morphologically and structurally using scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS) and X-ray diffraction analysis (XRD). The degradation behaviour of the M/C joints was assessed by means of electrochemical techniques. It was found that a brazing temperature of 850°C and a holding time of 2.4 ks, produces the best results in terms of bond strength, 130 ± 16 MPa. The mechanical properties obtained could be explained on the basis of the different compounds identified on the fracture surfaces by XRD. On the other hand, a brazing temperature of 950°C produces the best results in terms of corrosion rates (lower corrosion current), 3.44 ± 0.73 A cm^–2. However, the joints produced at 850°C using a holding time of 1.2 ks present the best compromise between mechanical properties and degradation behaviour, 122 ± 12 MPa and 7.59 ± 1.47 A cm^–2 respectively. The role of Ti diffusion from the metallic Ti to the Al₂O₃ surface is fundamental in terms of the final value achieved for the M/C bond strength. On the contrary, the Ti distribution along the brazed interface does not seem to play any relevant role in the M/C joints electrochemical performance.     

Effect of ZrN coating by magnetron sputtering and sol–gel processed silica coating on titanium/porcelain interface bond strength

In this study, a coating technique was applied to improve the bond strength of titanium (Ti) porcelain. ZrN coating was prepared by magnetron sputtering, and silica coating was processed by a sol–gel method. The treated surfaces of the specimens were analyzed by X-ray diffraction, and the Ti/porcelain interface was investigated by scanning electron microscopy (SEM) and energy dispersive spectroscopy. The coated specimens appeared fully coherent to the Ti substrate. The fractured bonding surface was also investigated by SEM. The residual porcelain on the metal surface could be observed in the ZrN group and silica group, but there was no obvious porcelain remaining in the control group. A three-point-bending test showed that the bonding strength of the ZrN group (45.99 ± 0.65 MPa) was higher than the silica group (37.77 ± 0.78 MPa) (P < 0.001) and control group (29.48 ± 1.01 MPa) (P < 0.001), while that of the silica group was significantly higher than the control group (P < 0.001). In conclusion, conditioning the ceramic surface with ZrN and silica coatings resulted in a stronger Ti/porcelain bond. ZrN coating by magnetron sputtering was a more effective way to improve the bond strength between Ti and porcelain compared with sol–gel processed silica coating in this study.     

Plasma-sprayed zirconia bond coat as an intermediate layer for hydroxyapatite coating on titanium alloy substrate

This study aims to strengthen the bonding at HA coating/Ti–6Al–4V interface by adding an intermediate ZrO₂ bond coat between them. The bonding strength of the HA/ZrO₂ coating was evaluated with the separately prepared HA coating as control. The phase, microstructure and chemistry, and surface roughness of the plasma-sprayed two-layer HA/ZrO₂ coating on Ti–6A1–4V substrate were investigated by X-ray diffractometry, scanning electron microscopy, and surfcorder, respectively. Experimental results indicate that the bonding strength increases from 28.6±3.22 MPa for HA coating to 36.2±3.02 MPa for HA/ZrO₂ composite coating. Elemental analysis employed on the surface of ZrO₂ bond coat, on which the HA top coat was first dissolved completely in HCl acid, reveals the sign of diffusion of calcium ions from HA to ZrO₂ bond coat. In addition, rougher surface morphology provided by ZrO₂ bond coat is also considered to aid in the bonding at HA/ZrO₂ interface. Similar coating system done by other researchers is compared and discussed.     

Microstructure and mechanical properties of ZrB2-SiC composites

A ZrB₂-based composite containing 20 vol.% nanosized SiC particles (ZSN) was fabricated at 1900 °C for 30 min under a uniaxed load of 30 MPa by hot-pressing. The microstructure and mechanical properties of the composite were investigated. It was shown that the grain growth of ZrB₂ matrix was effectively suppressed by submicrosized SiC particles located along the grain boundaries. In addition, the mechanical properties of ZSN composite were strongly improved by incorporating the nanosized SiC particles into a ZrB₂ matrix, especially for flexural strength (925 ± 28 MPa) and fracture toughness (6.4 ± 0.3 MPa•m^1/2), which was much higher than that of monolithic ZrB₂ and ZrB₂-based composite with microsized SiC particles, respectively. The formation of intragranular nanostructures plays an important role in the strengthening and toughening of ZrB₂ ceramic.     

Microstructure and mechanical properties of yttria-stabilized tetragonal zirconia polycrystals containing dispersed TiC particles

The microstructure and mechanical properties of hot-pressed yttria-stabilized tetragonal zirconia polycrystals (Y-TZP) ceramics containing up to 30 vol % TiC particles were studied. Adding TiC particles to Y-TZP improved the bending strength and fracture toughness. With 20 vol% TiC particles the maximum bending strength and fracture toughness reached 1073±30.4 MPa and 14.56±0.25 MPa m^1/2, respectively. The residual tensile stress induced by the thermal expansion difference between ZrO₂ and TiC must have inhibited the tetragonal-monoclinic transformation. The stress-induced phase transformation was therefore not the dominant toughening mechanism. High-densities of dislocations within TiC particles and microcracking were detected by TEM. The improved toughness of the materials is considered to be the result of crack deflection, crack bowing of TiC particles and microcracking toughening of ZrO₂.     

The displacive compensation of porosity (DCP) method for fabricating dense, shaped, high-ceramic-bearing bodies at modest temperatures

A novel process is introduced for the fabrication of dense, shaped ceramic/metal composites of high ceramic content: the Displacive Compensation of Porosity (DCP) method. In this process, a metallic liquid is allowed to infiltrate and undergo a displacement reaction with a porous oxide preform. Unlike other displacement-reaction-based processes (e.g., the C⁴, RMP, and AAA processes), a larger volume of oxide is generated than is consumed, so that composites with relatively high ceramic contents can be fabricated. Bar- and disk-shaped MgO/Mg-Al composites were produced by the infiltration and reaction of molten Mg with porous Al₂O₃ preforms at 1000 °C. By varying the relative density of the preforms (from 53.3 to 71.0% of theoretical), the magnesia content of the final composites could be adjusted from 70.4 to 85.6 vol %. Because the increase in oxide volume associated with the conversion of alumina into magnesia was accommodated by the prior pore volume of the preforms, the composites retained the shapes and dimensions (to within a few percent) of the starting preforms. The MgO/Mg-Al composites were lightweight (2.94–3.30 g/cm³), dense (97.7–99.0% of theoretical), and resistant to hydration. Bar-shaped MgO/Mg-Al composites exhibited average flexural strength and indentation toughness values of 244 MPa and 5.4 MPa · m^1/2, respectively.     

Synthesis and mechanical properties of high-purity Cr2AlC ceramic

High-purity and dense Cr₂AlC has been successfully fabricated by hot-pressing, using Cr, Al and graphite as raw materials. Delamination, kink bands, monolamellar kink, transgranular crack and transgranular fracture of bulk Cr₂AlC are found during the room-temperature test. The density, Vickers hardness, flexural strength, Young's modulus, compressive strength and fracture toughness of the Cr₂AlC are 5.17 g/cm³, 4.9 GPa, 469 ± 27 MPa, 282 GPa, 949 ± 22 MPa and 6.22 ± 0.26 MPa m^1/2, respectively. The strength of Cr₂AlC could be greatly improved by second phase of Cr₇C₃. And the slipping of basal planes and slip system cold be hindered by Cr₇C₃, thus resulting in a lower toughness.     

Evaluation of Si3N4 joints: bond strength and microstructure

Joining of pressurelessly sintered silicon nitride ceramics was carried out using adhesive slurries in the system Y-Si-Al-O-N in a nitriding atmosphere. The effects of bonding parameters, such as joining temperature (1450–1650°C), applied pressure (0– MPa) and holding time (10–60 min), on the bond strength of joint were evaluated. A typical microstructure of the joint bonded with the optimum adhesive was investigated. The three point bend testing of joined samples with 3 × 4 × 36 mm³ in dimension was employed to study the bond strength of joints. The results show that an optimum joining process was achieved by holding at 1600°C for 30 min under an external pressure of 5 MPa and the maximum bond strength was 550 MPa, compared to 700 MPa of unbonded Si₃N₄ ceramic, using the adhesive having the Si₃N₄/(Y₂O₃ + SiO₂ + Al₂O₃) ratio of 0.39. The good bond strength is attributed to the similarity in microstructure and chemical composition between joint zone and ceramic substrate. The fracture modes were classified into two types according to the values of bond strength. This revised version was published online in September 2006 with corrections to the Cover Date.     

Computational modeling of debonding behavior at the bone/cement interface with experimental validation

Both clinical examinations and in vitro physical experiments have shown that the fixation interfaces of cemented components are actually critical sites affecting the long-term stability and survival of prosthetic implants after implantation. This study aims to investigate the interfacial debonding behavior of bone/cement composite structures and attempts to establish an analysis model for clinical applications involving cemented prosthetic components. The mechanical properties of the bonded interface were characterized by interfacial strength, interfacial stiffness, and fracture toughness; the measured values of tensile strength, shear strength, and fracture toughness were 4.94 MPa, 5.94 MPa, and 0.34 MN/m^3/2, respectively. The measured strengths of the different configurations from this study are in good agreement with the experimental results available in the literature. In addition, we generated a finite element model with the same geometry as that of the experimental specimen used in the fracture test. The extent of interfacial debonding was further determined by means of the surface damage criteria and the fracture characteristics of the interface crack. The finite element model with an elastic interface predicted that the stress intensity factor (SIF) at the bone/cement interface crack varies nonlinearly with the applied load, which shows that the interface disintegrates at the load level, as was measured in the fracture experiments. It was possible to verify that the proposed simulation model was capable of describing the interfacial mechanical behavior of cemented components.     

AlN与Mo-Ni-Cu活性封接的微观结构和性能分析

AlN陶瓷是一种性能优良的电子封装材料,但不容易与金属直接连接在一起.实验采用98（Ag28Cu）2Ti活性焊料, 在真空条件下实现了AlN陶瓷与Mo Ni Cu合金的活性封接.利用EBSD、EDS、XRD方法研究了焊接区域以及剪切试样断裂表面的微观结构和相组成,测定了焊区的力学性能和气密性.研究结果显示：在AlN陶瓷界面上有TiN生成,说明陶瓷与焊料之间是一种化学键合,而在Mo Ni Cu合金的界面上有少量的Ni Ti金属间化合物存在.剪切后试样的断裂面上有TiN和AlN,说明断裂发生在靠近陶瓷的焊层区域.焊接试样性能优良：气密性达到1.0×10^-11Pa·m³/s,平均抗弯强度σ_ｂ=78.55MPa,剪切强度σ_τ=189.58MPa.     

The thermal shock resistance of the ZrB2–SiC–ZrC ceramic

In the present work, the thermal shock resistance of the ZrB₂–SiC–ZrC ceramic was estimated by the water quenching method and the flexural strength of the quenched specimen was measured. The measured critical temperature difference of the ZrB₂–SiC–ZrC ceramic was significantly greater than that of the ZrB₂–15 vol.% SiC ceramic. The improvement in thermal shock resistance was attributed to its higher fracture toughness (6.7 MPa m^1/2) and lower flexural strength (526 MPa) relative to the ZrB₂–15 vol.% SiC ceramic (4.1 MPa m^1/2 and 795 MPa) based on Griffith fracture criterion. Furthermore, the temperature and thermal stress distributions in the specimen during instantaneous water quenching were simulated by Finite element analysis.     

Influence of interfacial bonding conditions on the anti-penetration performance of ceramic/metal composite targets

This study analyzes the influence of bonded and unbonded interface conditions on the anti-penetration performance of a ceramic/metal composite target and determines the associated mechanism. The 3D finite element and 3D smoothed particle hydrodynamics simulation results revealed that a bonded ceramic/metal target exhibited better anti-penetration performance than an unbonded target, and the associated mechanism was determined. Notably, the bond strength between the ceramic and metal backplate plays an important role in the formation of the ceramic conoid, and the ceramic conoid that formed in the bonded target effectively consumed the kinetic energy of the projectile, thereby improving the anti-penetration performance of ceramic composite armor. To verify this conclusion, we also compare and analyze the anti-penetration performance of interface bonded and unbonded metal/metal composite targets. The results show that due to the absence of the ceramic conoid, the interfacial bonding conditions have little influence on the anti-penetration performance of a metal/metal composite target.

     

Comparison of failure mechanisms for cements used in skeletal luting applications

Glass Polyalkenoate Cements (GPCs) based on strontium calcium zinc silicate (Sr–Ca–Zn–SiO₂) glasses and low molecular weight poly(acrylic acid) (PAA) have been shown to exhibit suitable compressive strength (65 MPa) and flexural strength (14 MPa) for orthopaedic luting applications. In this study, two such GPC formulations, alongside two commercial cements (Simplex^® P and Hydroset?) were examined. Fracture toughness and tensile bond strength to sintered hydroxyapatite and a biomedical titanium alloy were examined. Fracture toughness of the commercial Poly(methyl methacrylate) cement, Simplex^® P, (3.02 MPa m^1/2) was superior to that of the novel GPC (0.36 MPa m^1/2) and the commercial calcium phosphate cement, Hydroset?, for which no significant fracture toughness was obtained. However, tensile bond strengths of the novel GPCs (0.38 MPa), after a prolonged period (30 days), were observed to be superior to commercial controls (Simplex? P: 0.07 MPa, Hydroset?: 0.16 MPa).