Interfacial reactions and bending strength of SiC/A356/FeNi50 composite fabricated by gas pressure infiltration

The SiC/A356/FeNi50 composite was fabricated by gas pressure infiltration. The interfacial region of the SiC/A356/FeNi50 composite consisted of FeNi50 reaction layer, A1 reaction layer and A1 alloy matrix. The main intermetallic compounds were （Fe,Ni）a（A1,Sih3 and （Fe,Ni）2（A1,Si）5 at the A1 reaction layer and FeNi50 reaction layer, respectively. The bending behavior versus different infiltration temperatures and holding times was also investigated. The bending strength at 670 ~C was the highest and close to the bending strength of A1 alloy （223 MPa）, and 46% of SIC/A356. The brittle intermetallic compounds existing at the interface induced the decreasing of the bending strength. The pores were reduced by adequate heating time due to the homogeneous temperature of preform, which was beneficial to improve the bending strength of the composite.

Interfacial reaction product and mechanical properties of the electron beam brazed K465 Ni-based superalloy joints

Ni-based superalloy K465 is brazed with BNi-2 filler metal by vacuum electron beam brazing （VEBB）. In process of VEBB, effects of processing primary parameters on shear strength of joints are investigated. Microstructure of the brazed joint with BNi-2 filler metal is studied by means of scanning electron microscopy （ SEM）, energy dispersive spectroscopy （EDS） and X-ray diffraction （XRD）. The results show that the structure of brazed seam consists of a large amount of Ni- based γ solid solution, Ni3Al （ γ＇） , Ni3B, WB, CrB, and a small quantity of WC, NbC, The maximum shear strength of the joint is 398 MPa when the beam current of welding is 2.6 mA, heating time is 480 s and focused current is 1 800 mA.

Adsorption Reaction Dynamics of Systems Lysozyme and Nanodiamond/Nanosilica at pH=7-13

Adsorption reactions between surfaces of nanodiamond and nanosilica with diameter of 100 nm prepared as suspension solutions of 0.25μg/μL and lysozyme molecule with different concentrations of 7 mmol/L PPBS at pH=7, 9, 11, and 13 have been investigated by fluores- cence spectroscopy. Adsorption reaction constants and coverages of lysozyme with different concentrations of 0-1000 nmol/L under the influences of different pH values have been ob- tained. Helicities and conformations of the adsorbed lysozyme molecules, free spaces of every adsorbed lysozyme molecule on the surfaces of nanopartieles at different concentrations and pH values have been deduced and discussed. The highest adsorption capabilities for both sys- tems and conformational efficiency of the adsorbed lysozyme molecule at pH=13 have been obtained. Lysozyme molecules can be prepared, adsorbed and carried with optimal activity and helicity, with 2 and 10 mg/m2 on unit nanosurface, 130 and 150 mg/g with respect to the weight of nanoparticle, within the linear regions of the coverages at around 150-250 nmol/L and four pH values for nanodiamond and nanosilica, respectively. They can be prepared in the tightest packed form, with 20 and 55 mg/m2, 810-1680 and 580-1100 mg/g at threshold concentrations and four pH values for nanodiamond and nanosilica, respectively.

Interfacial Reaction Between Solid Nickel and Liquid Zinc

Interfacial reactions between solid nickel and liquid zinc at 450-650 ℃ for 30-600 s were studied. The morphology and growth behavior of intermetallic compound layers at the interface between solid nickel and liquid zinc were observed and analyzed by SEM and EDS. The results show that γ and 8 phases are formed at 450 ℃ at the Ni/Zn interface, and at 550 ℃ and 650 ℃ only ）,phase is formed at the interthce and some δ phase particles will be participated during solidification on the surface of γphase layer. The β1 phase is absent under experimental conditions. Many cracks occur in the layers due to the difference in thermal expansion coefficients of these phases. It is found that the kinetics of the intermetallic compounds growth follows a parabolic law of time, as controlled by the diffusion mechanism. The apparent activation energies are 113.9 kJ/mol for the growth of γphase and 125.87 kJ/mol for γ1 phase, respectively.

Microstructure and interface thermal stability of C/Mo double-coated SiC fiber reinforced γ-TiAl matrix composites

C/Mo duplex coating interfacially modified SiC fiber-reinforced γ-TiAl matrix composite （SiCf/C/Mo/γ-TiA1） was prepared by foil-fiber-foil method to investigate its interfacial modification effect. SiCf/C/TiAl composites were also prepared under the same processing condition for comparision. Both kinds of the composites were thermally exposed in vacuum at 800 and 900℃ for different durations in order to study thermal stability of the interfacial zone. With the aids of scanning electron microscope （SEM） and energy dispersive spectrometer （EDS）, the interracial microstructures of the composites were investigated. The results reveal that, although adding the Mo coating, the interfacial reaction product of the SiCf/C/Mo/TiAl composite is the same with that of the SiCf/C/TiA1 composite, which is TiC/Ti2AlC between the coating and the matrix. However, C/Mo duplex coating is more efficient in hindering interfacial reaction than C single coating at 900 ℃ and below. In addition, a new layer of interfacial reaction product was found between Ti2AlC and the matrix after 900 ℃, 200 h thermal exposure, which is rich in V and close to the chemical composition of B2 phase.

Study on NiO/Fe interface with X-ray photoelectron spectroscopy

Different monolayers （ML） of Fe atoms were deposited on NiO （001） substrates or NiO underlayers using molecular beam epitaxy （MBE）, pulse laser deposition （PLD）, and magnetron sputtering （MS）. The magnetic properties and microstructure of the films were studied. The apparent magnetic dead layer （MDL） is found to exist at the NiO/Fe interfaces of the MBE sample （about 2 ML MDL）, the PLD sample （about 3 ML MDL）, and the MS sample （about 4 ML MDL）. X-ray photoelectron spectroscopy indicates the presence of ionic Fe （Fe2＋ or Fe3＋） and metallic Ni at the NiO/Fe interfaces, which may be due to the chemical reactions between Fe and NiO layers. This also leads to the formation of MDL. The thickness of the MDL and the reaction products are related with the deposition energy of the atoms on the substrates. The interfacial reactions are effectively suppressed by inserting a thin Pt layer at the NiO/Fe interface.

Research Progress of Interfacial Chemism of High Efficiency Organic Grinding Fluid for Si_3N_4 Ceramics

Grinding is a most important machining method for Si3N4 ceramics. Utilizing interracial chemistry reaction membrane between grinding fluid and Si3N4 ceramics can reduce friction factor, soften surface layer and meanwhile improve the grinding efficiency, which is a bran-new research direction. This article, based on high efficiency grinding of Si3N4 ceramics by the way of half plasticity removal, descanted on the assistant function of interface chemistry reaction to improve the removal rate of Si3N4 ceramics in the application of organic grinding fluids represented by alcohols grinding fluid. To target action mechanism research, it applies the methods of classification, comparison and induction, and advanced test equipments to explore the effects of long, short carbochain alcohol and their water solutions acting as grinding fluids. In addition, it also discusses the effective function of three groups of organic matters such as perhalogeno hydrocarbon, cationic surfactant and tetra ethoxysilane acting as grinding fluid components from different angles, reveals their mechanisms of action, and supplies theoretical basis for the development of machining ceramic grinding fluid of high efficiency, low cost.

Joining of C_f/SiBCN composite with two Ni-based brazing fillers and interfacial reactions

G/SiBCN ceramic composite was joined using Ni-19Cr-10Si （BNi5） and Ni-33Cr-24Pd-3.5Si-0.5B filler alloys at 1170 ℃ for 10 min. Two kinds of Ni-based filler alloys exhibited good wettability on the CdSiBCN com- posite, with a contact angle of 13° and 4°, respectively, The microstructures of the brazed joints were investigated by electron-probe microanalysis （EPMA）, and three-point bend test was conducted for the joints at room temperature. When being brazed with BNi5 filler alloy, no evident reaction layer was ob- served at the surface of the joined composite, and the joint microstructure was characterized by Ni2Si matrix with scatteringly distributing mixture compounds of Cr23C6, Ni2Si and CrB. While Ni-Cr-Pd（Si,B） brazing alloy was used, a Cr23C6 reaction layer with a thickness of 11 μm was formed at the surface of the base composite. In the central part of the brazed joint, the phases were composed of Ni（Cr, Si） solid solution and complex compounds including Pd2Si, （Ni,Pd）2Si and Ni-B. The strength of Cf/SiBCN joint brazed with BNi5 filler alloy was 62.9 MPa at room temperature, whereas that with Ni-Cr-Pd（Si,B） filler alloy was at the same level.

Solid-Liquid State Bonding of Si3N4 Ceramics with Ceramic-Modified Brazing Alloy

Solid-liquid state bonding of Si3N4 ceramics with TiN-modified Ag-Cu-Ti brazing alloy was used'- to enhance joint strength. The effects of the TiN particles on the microstructures, interfacial reactions, and room-temperature properties of the joints were investigated. The results show that the TiN particles are gen- erally well dispersed in the Ag-Cu eutectic base and the interface between them is both clean and com-pact. Changes in the TiN volume fractions from 0 to 20% exert no noticeable effect on the interfacial reac-tion between Ag-Cu-Ti and the substrates. Other bonding parameters being constant, the TiN volume frac-tion in the filler material plays a key role in the joint properties. For TiN volume fractions below 20%, the joints are reinforced, especially joints with 5% and 20% TiN. The average shearing strength of joints with 5% TiN is 200.8 MPa, 30% higher than that of joints with no TiN (154.1 MPa). However, for TiN volumes frac- tions above 20%, the joint strengths decrease.

Microstructure and Property of AlN Joint Brazed with Au–Pd–Co–Ni–V Brazing Filler

An Au-Pd-Co-Ni-V brazing alloy was designed for AIN ceramic joining. Its wettability on AIN was studied with the sessile drop method. The results showed that the contact angle was decreased gradu- ally with increasing temperature and the prolonging of holding time. Sound AIN/AIN joints were achieved with the brazing alloy at 1170 ℃ for 10 min. The microstructure of the AIN/AIN joints was examined by scanning electron microscopy （SEM）. It was found that element V played the active role in the interfacial reaction between the ceramic and the brazing alloy, V reacted with N decomposed from AIN, resulted in the formation of V-N compound. Based on the energy-dispersive spectroscopy （EDS） and X-ray diffraction （XRD） analysis results, the V-N reaction product was verified as V2N. The overall reaction during the brazing process can be described by the following equation： 2V ＋ AIN ＋ 2Pd = V2N ＋ Pd2AI. The AIN/AIN joints brazed with the Au-Pd-Co-Ni-V brazing alloy exhibited three-point bend strength of 162.7 MPa at room temperature, and under the bend test the fracture of the joint occurred at the AIN ceramic substrate.