Effect of TiO2 addition and high magnetic field sintering on properties of vitrified bond CBN composites

Vitrified bond CBN composites, with different amounts of TiO₂ doping, were prepared by conventional sintering and high magnetic field sintering processes. Mechanical properties, cross-sectional morphology, refractoriness, fluidity and structural characterization have been carried out to understand the role of TiO₂ addition and sintering conditions. Results show that TiO₂ addition significantly affected bending strength, refractoriness and fluidity of vitrified bonds. In addition, high magnetic field sintering improved bending strength and the microstructure of vitrified bond CBN composites. Due to high magnetic field sintering, CBN grains were completely covered by vitrified bond and exhibited fewer pores. In addition, high magnetic field promoted the growth of specific grains, such as SiO₂, whereas suppressed grain growth of other crystal phases, such as NaAlSi₃O₈.     

Influence of TiO2 on the physical properties of low-temperature ceramic vitrified bond and mechanical properties of CBN composites

The microstructures and properties of vitrified bond abrasive tools made of CBN grains and advanced vitrified bond systems with different TiO₂ doping amounts were investigated. Based on the experimental observations and analysis, the incorporation of TiO₂ in appropriate amount (4 wt.%) was beneficial to the improvement on flowing ability and thermal expansion property of the vitrified bond systems, and mechanical properties of the CBN composites including bending strength and Rockwell hardness were obviously improved. On the basis of discussion for microstructure, the CBN grains were better covered by vitrified bond and acquired less pores when the content of TiO₂ reached 4 wt.%. These results were related to the role of TiO₂ in the glass network structure which was analyzed by Fourier transform infrared spectroscopy (FTIR).     

Effects of Al2O3 addition on sintering behaviour,microstructure, and physical properties of Al2O3/vitrified bond CBN composite

The effects of Al₂O₃ content on the sintering behaviour, microstructure, and physical properties of Al₂O₃/vitrified bonds (SiO₂–Al₂O₃–B₂O₃–BaO–Na₂O–Li₂O–ZnO–MgO) and Al₂O₃/vitrified bond cubic boron nitride (CBN) composites were systematically investigated using X-ray diffraction, differential scanning calorimetry, dilatometry, scanning electron microscopy, and X-ray photoelectron spectroscopy. Various amounts of Al₂O₃ promoted the formation of BaAl₂Si₂O₈ and γ-LiAlSi₂O₆, increasing the relative crystallinity of the Al₂O₃/vitrified composite from 85.0 to 93.2%, resulting in residual compressive stress on BaAl₂Si₂O₈, thereby influencing the thermal behaviour and mechanical properties of the Al₂O₃/vitrified composite. The bulk density, porosity, flexural strength, hardness, and thermal conductivity of 57.5 wt% Al₂O₃ sintered at 950 °C were 3.12 g/cm³, 6.1%, 169 MPa, 90.5 HRC, and 4.17 W/(m·K), respectively. The coefficient of thermal expansion of the bonding material was 3.83 × 10^?6 °C^?1, which was comparable to that of CBN, and the number of N–Al bonds were increased, which boosted the flexural strength of the Al₂O₃/vitrified CBN composite to 81 MPa. The excellent mechanical properties, compact structure, and suitable interfacial bonding state with the CBN grains of the Al₂O₃/vitrified composite make it a promising high-performance bonding material for superhard abrasive tools.     

Variations in structure and properties of vitrified bonds and vitrified diamond composites prepared by sol-gel and melting methods at different sintering temperature

Differences in structure and properties of Na₂O–Al₂O₃–B₂O₃–SiO₂ vitrified bonds and vitrified diamond composites prepared by sol-gel and melting methods were methodically discussed. Results showed that the vitrified bond prepared by sol-gel method contained more [AlO₄] tetrahedron and owned higher bending strength, with the maximum value reaching 137 MPa, 31.73% higher than that prepared by melting method (104 MPa). As the sintered temperature rose, coefficient of thermal expansion of the vitrified bond prepared by sol-gel method increased first and then decreased, acquiring a maximum value of 5.75 × 10⁻⁶ °C ⁻¹ at 720 °C, which was still much lower than the minimum value of vitrified bond prepared by melting method (7.02 × 10⁻⁶ °C ⁻¹). The vitrified diamond composite prepared by sol-gel method possessed lower sintering shrinkage than that prepared by melting method, and could be applicable to the production of grinding tools with high dimensional accuracy. What's more, the maximum bending strength of vitrified diamond composites obtained by sol-gel method was 106 MPa, 24.7% higher than that of vitrified diamond composites prepared by melting method (85 MPa).     

Effects of Y2O3 addition on structure and properties of LZAS vitrified bond for CBN grinding tools application

The effects of Y₂O₃ addition on the structure and properties of Li₂O–ZnO–Al₂O₃–SiO₂ (LZAS) vitrified bonds were firstly investigated for CBN grinding tools application. Glasses and glass-ceramics were characterized using differential scanning calorimetry, X-ray diffractometry, scanning electron microscopy and infrared spectroscopy. The thermal expansion coefficient (TEC), microhardness, bending strength and chemical durability of the obtained products were also evaluated. Results showed that Y₂O₃ acted as the network former in the track of SiO₄ tetrahedrals. Introducing Y₂O₃ in the glasses increased the glass transition temperature and crystallization temperature. The crystallization of the main β-quartz_ss phase increased with increase of Y₂O₃ content. The morphology of the crystals was dependent on the Y₂O₃ content. The TEC (5.15×10⁻⁶/°C) of vitrified bond containing 1.0 mol% Y₂O₃ (Y1.0) was very close to the TEC (5.0×10⁻⁶/°C) of CBN grains. Moreover, Y1.0 vitrified bond exhibits a high microhardness (5.98 GPa), a high bending strength (202 MPa) and a good chemical durability (20 days, DR=2.8×10⁻⁹ g/cm² min), suggesting that it would be a promising material for CBN grinding tool.     

Effects of sintering in a high magnetic field on properties of vitrified bond and vitrified CBN composites

Vitrified bond CBN grinding wheels are being widely used due to their superior performance. Also, advantages of vitrified grinding wheels are high elastic modulus, stable chemical property, and low thermal expansion coefficient. Brittleness and low strength are key factors restricting the development of vitrified bond CBN grinding wheels. In this paper, the sintering in a high magnetic field was innovatively introduced into the manufacturing of vitrified bond CBN grinding wheels, and the effects of sintering in a high magnetic field on properties on vitrified bond and vitrified CBN composites were systematically investigated. Vitrified bond was characterized using three-point bending, scanning electron microscopy, X-ray diffraction. It was observed that microstructure of vitrified bond could be changed, grain orientation could be controlled and average grain size could be decreased in a high magnetic field, while vitrified bond strength could be simultaneously improved. High quality vitrified bond could be obtained by appropriately adjusting the strength and direction of high magnetic field. Results demonstrated that vitrified bond properties were improved when the magnetic field strength was 6?T. In order to highlight the high magnetic field effect on the vitrified CBN composites, the ordinary CBN abrasives and nickel plated CBN abrasives were used respectively. Microstructures, bending strengths of vitrified CBN composites were compared in different high magnetic fields. When the magnetic field strength was appropriate (less than 6?T), the binding characteristic of vitrified bond CBN composites with nickel plated CBN abrasives was greatly improved. The highest bending strength value of vitrified CBN composites was 79.5?MPa in 6?T high magnetic field.     

Effects of Ni addition on properties of vitrified bond CBN composites in strong magnetic field

Properties of vitrified bond with varying Ni doping amounts were extensively investigated. Effects of Ni addition on microstructures and properties of vitrified bond cubic boron nitride (CBN) composites prepared in strong magnetic field were investigated for applications in CBN grinding tools. Vitrified bond was characterized using three-point bending, scanning electron microscopy, X-ray diffraction and other methods. The refractoriness, fluidity, and bending strength of vitrified bond were evaluated. Bending strengths, microstructures, and phase compositions of vitrified bond CBN composites achieved using conventional and strong electromagnetic sintering techniques were compared. Results show that the addition of Ni to vitrified bond CBN composites improved the fluidity and bending strength of the vitrified bond. Strong electromagnetic sintering improved the mechanical strength and pore structure of vitrified bond CBN composites. Moreover, the introduction of the strong magnetic field facilitated Ni migration and aggregation in vitrified bond, rotated abrasives, and formed new substances, thus increasing the stability of vitrified bond CBN composite thermal material. Also, strong magnetic field inhibit grain growth of non-magnetic and ferromagnetic materials with fine-grain effect.     

Sintering,microstructure, and mechanical properties of vitrified bond diamond composite

The demand for high-performance grinding wheels is gradually increasing due to rapid industrial development. Vitrified bond diamond composite is a versatile material for grinding wheels used in the backside grinding step of Si wafer production. However, the properties of the vitrified bond diamond composite are controlled by the characteristics of the diamond particles, the vitrified bond, and pores and are very complicated. The main objective of this study was to investigate the effects of SiO₂–Na₂O–B₂O₃–Al₂O₃–Li₂O–K₂O–CaO–MgO–ZrO₂–TiO₂–Bi₂O₃ glass powder on the sintering, microstructure, and mechanical properties of the vitrified bond diamond composite. The elemental distributions of the composite were analyzed using electron probe micro-analysis (EPMA) to clarify the diffusion behaviors of various elements during sintering.The results showed that the relative density and transverse rupture strength of the composite sintered at 620 °C were 91.7% and 126 MPa, respectively. After sintering at 680 °C, the glass powder used in this study exhibited a superior forming ability without an additional pore foaming agent. The relative density and transverse rupture strength of the composite decreased to 48.2% and 49 MPa, respectively. Moreover, the low sintering temperature of this glass powder protected the diamond particles from graphitization during sintering, as determined by X-ray diffraction and Raman spectrum. Furthermore, the EPMA results indicate that Na diffused and segregated at the interface between the diamond particles and vitrified bond, contributing to the improved bonding. The diamond particles can remain effectively bonded by the vitrified bond even after fracture.     

Preparation and characterization of vitrified CeO2 coated cBN composites

The performances of vitrified cBN composites are deeply affected by the wettability of vitrified bonds on cBN particles. CeO₂ coated cBN particles were successfully prepared for the further improvement of the covering and wetting of cBN by vitrified bonds. The microstructure and properties of vitrified cBN composites were characterized by scanning electron microscope (SEM), hot stage microscope (HSM), transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and flexural strength. Results showed that the prepared CeO₂ coating on the surface of cBN was uniform and dense. Besides, the improved wettability of vitrified bonds on CeO₂ coated cBN particles accompanied with the formation of Ce–O–Al and N–Si confirmed by XPS were supposed to conduce to enhancing the holding power of the vitrified bonds to cBN particles, which resulted in increasing the flexural strength of vitrified cBN composites by 9.16%. Thus, coating cBN with CeO₂ was a potential and effective method to obtain vitrified cBN composites with higher flexural strength.     

Influence of holding time on the interfacial solid solution and mechanical properties of agglomerated white fused alumina abrasives

In this paper, the aging relationship between holding time and the interfacial solid solution was utilized to prepare high-performance agglomerated white fused alumina (AWA) abrasives. The influence of holding time on the interfacial solid solution and mechanical properties of AWA abrasives were systematically investigated, and the grinding performance was thoroughly analyzed. The results showed that increasing the holding time caused the Al₂O₃ to violently infiltrate the interface between the white fused alumina (WA) particles and the vitrified bond, which led to the precipitation of a large amount of β-spodumene and monoclinic celsian in the vitrified bond and transformed the simple mechanical bonds between the WA particles and the vitrified bond into stronger chemical bonds. Thus, it was possible to control the mechanical properties of the AWA abrasives by adjusting the holding time. Specifically, after sintering at 760 °C for 4h, the single particle compressive strength and impact toughness reached the maximum values of 26 N and 63%, respectively. In comparison with the WA grinding wheel, the grinding ratio of the AWA grinding wheel was increased by 17.9% and the workpiece surface roughness was reduced by 21.1%.     

Effect of polycrystalline mullite fibers on the properties of vitrified bond and vitrified CBN composites

The effect of polycrystalline mullite fibers (PMFs) on the properties of vitreous bonds and vitrified CBN composites was investigated. The results show that the addition of PMFs can increase the porosity of composites and reduce the fluidity of binders. The vitrified composites incorporating 6.4 wt% PMFs display excellent mechanical strength, which is enhanced by 21.2% compared with that of composites without PMFs sintered at the optimal sintering temperature. Meanwhile the thermal expansion coefficient of vitrified bond reduces from 6.256×10⁻⁶ °C⁻¹ to 4.805×10⁻⁶ °C⁻¹ with increasing fraction of PMFs. The improvement of mechanical strength is associated with the change of cracking mechanisms of the composites with fibrous crystals and the existence of several observed mechanisms, including fiber pull-out, fiber bridging and rupture.     

Preparation of a novel vitrified bond CBN grinding wheel and study on the grinding performance

The vitrified bond CBN grinding wheels are characterized by high efficiency, high precision, and low environmental pollution. In recent years, the vitrified bond CBN grinding wheel has been widely used in manufacturing industries such as aerospace, automotive, and machine tools. In this study, a novel vitrified bond formulation containing nano SiO₂ and nano CeO₂ is selected to prepare the grinding wheel. The grinding experiments on 45# steel and YG20 alloy indicate that the grinding performance of the nano vitrified bond grinding wheel is significantly better than that of the conventional vitrified bond grinding wheel. The introduction of nano SiO₂ and nano CeO₂ greatly improves the machining performance of the vitrified bond CBN grinding wheel.     

金属铝粉和纳米Al2O3粉对陶瓷结合剂性能的影响

将金属铝粉、纳米Al₂O₃粉引入基础陶瓷结合剂,通过红外光谱分析陶瓷结合剂玻璃结构,X射线衍射表征其物相变化,并测试其耐火度,利用扫描电镜分析陶瓷结合剂立方氮化硼(CBN)复合材料的微观结构,并测试抗折强度,系统分析了金属铝粉、纳米Al₂O₃粉的单掺及复掺对陶瓷结合剂性能的影响。结果表明,金属铝粉使陶瓷结合剂耐火度升高,玻璃结构没有明显改变,部分铝粉转变为Al₂O₃,添加金属铝粉的陶瓷结合剂CBN复合材料抗折强度随烧结温度升高而提高。纳米Al₂O₃粉使陶瓷结合剂耐火度降低,呈玻璃相,但有少量Al₂SiO₅晶体和Li_xAl_xSi_3-xO₆晶体析出,添加纳米Al₂O₃粉的陶瓷结合剂CBN复合材料烧结温度720 ℃时出现较高抗折强度,达93.7 MPa。金属铝粉和纳米Al₂O₃粉的复掺有利于玻璃网络结构的键合,陶瓷结合剂以玻璃相为主,也有少量晶体析出,二者复掺对提高陶瓷结合剂CBN复合材料抗折强度更有优势,但烧结温度也相应升高,烧结温度740 ℃时抗折强度达最高值,为97.4 MPa。     

Effect of nano-AlN addition on thermal diffusivity and mechanical strength of porous AL2O3 ceramic composites

In a properly made porous abrasive composite, the vitrified bond should ideally cover the grains and form a continuous network of bridges, and thus part of the heat energy from the grinding process is also transferred to the vitrified bond. Until recently, most studies on the design of composite properties have focused mainly on improving their mechanical strength and wear resistance, but increasingly the very important aspect of their thermal properties is noticed. The vitrified Al₂O₃ composites were made from Al₂O₃ grains, vitrified bond of Na₂OK₂OAl₂OB₂O₃SiO₂ and AlN nanopowder. The increase in porosity in the tested composites is the effect of the AlN decomposition reaction. Crystalline phases were identified in both composites - α-Al₂O₃ and NaAl₁₁O₁₇, but with a different percentage share in individual composites. In composites doped with AlN nanopowder, the proportion of NaAl₁₁O₁₇ crystalline phase decreases, due to its high susceptibility to reduction by Al, obtained from the AlN decomposition reaction. The product of the redox reaction is also Na⁺ ions, which may participate in the formation of the glass phase and thus increasing the fraction of the residual glass phase. As a result of the partial reduction of NaAl₁₁O₁₇ phase, an increase in α-Al₂O₃ content is observed. A higher proportion of α-Al₂O₃ phase with high thermal conductivity can be a factor that increases the rate of heat removal from the work zone.     

Effect of Yb2O3 and TiO2 on reaction sintering and properties of magnesium aluminate spinel

Magnesium aluminate spinel with an initial MgO: Al₂O₃ molar ratio of 2:1 was prepared from its constituent oxides through a solid-state sintering process at temperatures ranging from 1550 to 1700 °C in a normal air atmosphere. The effect of varying amount (0.25–1.0 wt%) of TiO₂ and Yb₂O₃ on densification, phase assemblage, mechanical, thermo-mechanical properties and microstructure of magnesia-rich spinel were investigated under static heating condition. The addition of TiO₂ and Yb₂O₃ favours the densification of magnesia-rich spinel, which is discernible up to 1650 °C. This beneficial effect may be attributed to the development of the secondary phase and formation of solid solution due to the dissolution of the additive ions in the spinel structure. A marginal increase in the average grain size of the samples along with a narrower grain size distribution occurred with the incorporation of both the additives. Both the additives improved the mechanical properties of the magnesia-rich spinel; however, better room temperature flexural strength was achieved with Yb₂O₃ as compared to TiO₂ addition. For the samples sintered at 1550 °C, 1.0 wt% Yb₂O₃ addition resulted in 30% increase in flexural strength; however, same amount of TiO₂ addition increased the strength by 20%. In case of thermal shock resistance, 1.0 wt% TiO₂ and 0.25 wt% Yb₂O₃ addition demonstrated promising result among all the samples.     

添加剂对CBN高速磨削工具用陶瓷结合剂熔融温度的影响

采用正交实验的方法分析了以SiO_2、Al_2O_3+B_2O_3为玻璃形成剂,MgO、P_2O_5、CaCO_3和ZnO四种添加剂对CBN陶瓷结合剂熔融温度的影响,并研究了添加这四种添加剂的陶瓷结合剂在高温下对CBN颗粒的润湿性.同时将其中的三组试样进行熔融、水淬,研究试样水淬前后熔融温度的变化,测定了熔融水淬后试样的物相组成.结果表明:四种添加剂对陶瓷结合剂熔融温度的影响大小为P_2O_5＞MgO＞＞ZnO ＞＞CaCO_3;熔融水淬后的试样化学成分均一,熔融温度降低,熔融试样呈玻璃态.     

Thermal stability and oxidation resistance of C/Al2O3 composites fabricated from a sol with high solid content

To improve fracture toughness of monolithic Al₂O₃ ceramics, three-dimensional carbon fiber preform was used as reinforcement, and the C/Al₂O₃ composites without interfacial coating were fabricated through vacuum impregnation-drying-heat treatment route with an Al₂O₃ sol as starting material. Characteristics of the Al₂O₃ sol with high solid content were firstly analyzed. Then thermal stability and oxidation resistance of the C/Al₂O₃ composites were investigated. It is found that the Al₂O₃ sol is an appropriate raw material for the fabrication of C/Al₂O₃ composites. The C/Al₂O₃ composites with a total porosity of 15.5% show a flexural strength of 208.5 MPa and a fracture toughness of 8.1 MPa m^1/2. Strength loss is observed after the composites were annealed at 1400 °C and 1600 °C under inert atmosphere. Oxidation resistance of the C/Al₂O₃ composites is unsatisfactory because of the existence of open pores and microcracks. When Al₂O₃ matrix was modified with SiO₂, the oxidation resistance is remarkably improved due to the viscous flow effect of SiO₂.     

An evaluation of plasma-sprayed coatings based on Al2O3 and Al2O3–13 wt.% TiO2 with bond coat on pure titanium substrate

In this study, the effects of bond coat on the properties of Al₂O₃ and Al₂O₃–13 wt.% TiO₂ coatings, which is plasma sprayed onto a commercial pure titanium substrate with and without Ni–5 wt.% Al (METCO 450 NS) as bond coating layer were investigated in terms of microhardness, bonding strength and surface roughness. Optical and scanning electron microscopy (SEM) examinations revealed that there is a uniform coating layer with no spalling and delamination. However, there is a little amount of porosity. The results indicated that the application of bond coat layer in the plasma spraying of Al₂O₃ and Al₂O₃–13 wt.% TiO₂ on pure titanium substrate has increased the hardness and bonding strength of coatings. While the adhesive bonding is dominant without bond coat, the cohesive bonding is dominant with the application of the bond coating layer. It has been observed that percentage of cohesion strength was about three times higher than that of adhesion strength.     

Processing and mechanical performance of 3D Cf/SiCN composites prepared by polymer impregnation and pyrolysis

The processing of 3D carbon fiber reinforced SiCN ceramic matrix composites prepared by polymer impregnation and pyrolysis (PIP) route was improved, and factors that determined the mechanical performance of the resulting composites were discussed. 3D C_f/SiCN composites with a relative density of ∼81% and uniform microstructure were obtained after 6 PIP cycles. The optimum bending strength, Young's modulus and fracture toughness of the composites were 75.2 MPa, 66.3 GPa and 1.65 MPa m^1/2, respectively. The residual strength retention rate of the as-pyrolyzed composites was 93.3% after thermal shock test at ΔT = 780 °C. It further degraded to 14.6% when the thermal shock temperature difference reached to 1180 °C. The bending strength of the composites was 35.6 MPa after annealing at 1000 °C in static air. The deterioration of the bending strength should be attributed to the strength degradation of carbon fibers and decomposition of interfacial structure.     

Microstructural evolution and interfacial reactions between Ti and ZrO2/CaTiO3 composites

Various proportions of ZrO₂/CaTiO₃ powders were mixed and hot pressed at 1500°C/30 min for Ti casting. The hot-pressed ZrO₂/CaTiO₃ composites were reacted with pure Ti at 1700°C/10 min in Ar. The interfacial reaction between Ti and ZrO₂/CaTiO₃ composites was investigated through X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and energy-dispersive X-ray spectroscopy. The ZrO₂/CaTiO₃ composites with less than 10 vol.%, CaTiO₃, and a minor amount of residual TiO₂ were found. When the content of ZrO₂ was increased to larger than 10 vol.%, two Ca₂Zr₅Ti₂O₁₆ and CaZrTi₂O₇ phases appeared in the composites. The amount of CaTiO₃ and CaZrTi₂O₇ in the composites gradually decreased as the amount of ZrO₂ increased. When Ti came in contact with ZrO₂/CaTiO₃ composites with less than 10 vol.% ZrO₂, the resulting eutectic reaction produced a liquid phase and induced melting. When ZrO₂ was increased to more than 30 vol.% in the composites, Ca₂Zr₅Ti₂O₁₆ and CaZrTi₂O₇ changed completely to CaZrO₃, Ti₂O, CaO, and ZrO₂. With more than 30 vol.% ZrO₂, no other reaction phases occurred in the Ti side after contact with the ZrO₂/CaTiO₃ composites, which is conducive for producing ceramic composites for Ti casting applications.