Effect of Sintering Temperature on Silver-Copper Nanopaste as High Temperature Die Attach Material

2013 ◽  
Vol 795 ◽  
pp. 47-50 ◽  
Author(s):  
Kim Seah Tan ◽  
Kuan Yew Cheong

A novel stencil-printable silver-copper (Ag-Cu) nanopaste that serves as an alternative high temperature die attach material was introduced in this study. The nanopaste was made by mixing 50 nm-sized of Ag and Cu particles with an organic binder system. Sintering temperatures, up to 450°C, were used to sinter nanopaste in air and its post sintered properties were investigated. The viscosity of nanopaste was 350,000 cps and it demonstrated a shear thinning behavior. Scanning electron microscope revealed the change of grain structure with the change in the sintering temperature. Formations of Ag97Cu3 and Ag1Cu99 compounds after sintering were confirmed with X-ray diffraction; and the electrical conductivity of the sintered nanopaste was increased with the increase of the sintering temperature. The study concluded 380°C was the optimum sintering temperature to form a well sintered nanopaste.

2013 ◽  
Vol 357-360 ◽  
pp. 1353-1357
Author(s):  
Xiao Li Ji ◽  
Zhuo Chen

High-temperature foam ceramics were produced from sludge, Zhongxiang porcelain sand, shale and sand, with addition of SiC 0.15%~0.40% as foaming agent, respectively, sintered at 1130°C~1160°C. The phase composition and micro structure of sintered samples were investigated by X-ray diffraction (XRD) and scanning electron microscopy (SEM), and density, compressive strength and thermal conductivity were evaluated. The results showed that the main phase of amorphous phase plagioclase in sintered samples and interior of samples with a large number of uniformly distributed closed pores, rose sintering temperature and increased SiC addition leading to pores size enlarged and density, compressive strength and thermal conductivity diminished.


2015 ◽  
Vol 804 ◽  
pp. 108-112 ◽  
Author(s):  
Thanapong Sareein ◽  
Panakamon Deeyai ◽  
Bundit Putasaeng ◽  
Naphat Chathirat

The high dielectric permittivity of Y2NiMnO6 ceramics were measured by Agilent E4294A (Impedance Measurement) range of frequency 100 to 10 MHz in this research. In this sample ceramics, passing by a sintering temperature of 1400°C at 6 hours to 24 hours. The phase and microstructure of the deposited materials were investigated as a function of sintering temperature, using X-ray diffraction (XRD) and scanning electron microscopy (SEM). We found that the dielectric properties are very sensitive to the several sintered follow by time, and high temperature can be related to the change ordering of Ni2+ and Mn4+ ions.


2014 ◽  
Vol 46 (1) ◽  
pp. 15-21 ◽  
Author(s):  
S. Islak ◽  
D. Kır ◽  
S. Buytoz

In this study, Cu-TiC composites were successfully produced using hot pressing method. Cu-TiC powder mixtures were hot-pressed for 4 min at 600, 700 and 800?C under an applied pressure of 50 MPa. Phase composition and microstructure of the composites hot pressed at different temperatures were characterized by X-ray diffraction, scanning electron microscope, and optic microscope techniques. Microstructure studies revealed that TiC particles were distributed uniformly in the Cu matrix. With the increasing sintering temperature, hardness of composites changed between 64.5 HV0.1 and 85.2 HV0.1. The highest electrical conductivity for Cu-10 wt.% TiC composites was obtained for the sintering temperature of 800?C, with approximately 68.1% IACS.


2012 ◽  
Vol 476-478 ◽  
pp. 1031-1035
Author(s):  
Wei Min Liu ◽  
Xing Ai ◽  
Jun Zhao ◽  
Yong Hui Zhou

Al2O3-TiC-ZrO2ceramic composites (ATZ) were fabricated by hot-pressed sintering. The phases and microstructure of the composites were studied by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The relative density and mechanical properties (flexural strength, fracture toughness and Vicker’s hardness) of the composites were tested. The results show that the microstructure of the composites was the gray core-white rim. With the increase of sintering temperature, the relative density and mechanical properties of the composites increased first and then decreased. The composite sintered at 1705°C has the highest synthetical properties, and its relative density, flexural strength, fracture toughness and Vickers hardness are 98.3%,970MPa,6.0 MPa•m1/2and 20.5GPa, respectively.


2015 ◽  
Vol 5 (01) ◽  
pp. 31
Author(s):  
Resky Irfanita ◽  
Asnaeni Ansar ◽  
Ayu Hardianti Pratiwi ◽  
Jasruddin J ◽  
Subaer S

The objective of this study is to investigate the effect of sintering temperature on the synthesis of SiC produced from rice husk ash (RHA) and 2B graphite pencils. The SiC was synthesized by using solid state reaction method sintered at temperatures of 750°C, 1000°C and 1200°C for 26 hours, 11.5 hours and 11.5 hours, respectively. The quantity and crystallinity level of SiC phase were measured by means of Rigaku MiniFlexII X-Ray Diffraction (XRD). The microstructure of SiC was examined by using Tescan Vega3SB Scanning Electron Microscopy (SEM). The XRD results showed that the concentration (wt%) of SiC phase increases with the increasing of sintering temperature. SEM results showed that the crystallinity level of SiC crystal is improving as the sintering temperature increases


2011 ◽  
Vol 335-336 ◽  
pp. 699-703
Author(s):  
Hui Hui Tan ◽  
Zhu Xing Tang ◽  
Xia Zhao ◽  
He Zhang

This paper introduces Si2ON2-SiC ceramic fabricated by pressureless sintering method and studies the effect of additives, nitriding temperatures on bulk density, porosity, phase composition and microstructure. It is discovered that additives MgO, CeO2 can increase the densities of Si2ON2-SiC ceramic apparently, and MgO additive has a better effect than CeO2. Nitriding temperature also is an important factor. The bulk density of the specimen with MgO additive reaches maximum at 1.91 g/cm3 when sintered at 1450 °C, and the bulk density of specimen with CeO2 additive is 1.86 g/cm3 at the same condition while the bulk density of the specimen without additive is only 1.75 g/cSuperscript textm3. The X-ray diffraction and scanning electron microscopy of the specimens show that the amount of Si2ON2 increase with the sintering temperature increase. But when the temperature is higher than 1500 °C the Si2ON2 grains will decompose into Si3N4, and Si2ON2 will vanish at 1550 °C


2007 ◽  
Vol 26-28 ◽  
pp. 243-246
Author(s):  
Xing Hua Yang ◽  
Jin Liang Huang ◽  
Xiao Wang ◽  
Chun Wei Cui

BaBi4-xLaxTi4O15 (BBLT) ceramics were prepared by conventional solid phase sintering ceramics processing technology. The crystal structure and the microstructure were detected by X-ray diffraction (XRD) and scanning electron microscope (SEM). The XRD analyses show that La3+ ions doping did not change the crystal structure of BBT ceramics. The sintering temperature increased from 1120°C to 1150°C with increasing Lanthanum content from 0 to 0.5, but it widened the sintering temperature range from 20°C to 50°C and refined the grain size of the BBT ceramic. Additionally, polarization treatment was performed and finally piezoelectric property was measured. As a result, the piezoelectric constant d33 of the 0.1at.% doped BBLT ceramics reached its highest value about 22pc/N at polarizing electric field of 8kV/mm and polarizing temperature of 120°C for 30min.


2011 ◽  
Vol 399-401 ◽  
pp. 855-859
Author(s):  
Ting Ting Wu ◽  
Bo Lin Wu

In order to improve the acid resistance and reduce the apparent density of fracturing proppants, TiO2 powder added in the system of BaO-MgO-Al2O3 fracturing proppants were prepared by the technique of pressureless sintering. The properties of the samples were investigated by the measurements of acid solubility, X-ray diffraction and scanning electron microscopy. The results show that the acid solubility of alumina matrix fracturing proppants contenting TiO2 of the 4wt% and BaO/MgO with the ratio of 3:7 is 0.15%. It is an important development in acid resistance performance of fracturing proppants research on laboratory. TiO2 is added to the raw materials and then calcine them to ceramics, which can reduces the sintering temperature, promote the densification and improve acid-resistant property of fracturing proppants.


2021 ◽  
Vol 1016 ◽  
pp. 379-384
Author(s):  
Eider Del Molino ◽  
Teresa Gutierrez ◽  
Mónica Serna-Ruiz ◽  
Maribel Arribas ◽  
Artem Arlazarov

The aim of this work was to study the influence of quenching and partitioning temperatures combined with various levels of Mn and Ni contents on the austenite stabilization along the quenching and partitioning (Q&P) cycle. Three steels with 2 wt.%, 4 wt.% and 6 wt.% manganese and one steel with 2 wt.% nickel content were investigated. Phase transformation temperatures and critical cooling rates were obtained experimentally using dilatometer for each alloy. Q&P cycles with different quenching and partitioning temperatures were also done in dilatometer, thus, allowing monitoring of the expansion/contraction during the whole Q&P cycle. Microstructure characterization was performed by means of a Scanning Electron Microscope and X-Ray Diffraction to measure retained austenite content. It was found that, strongly depending on the Q&P conditions, austenite stabilization or decomposition occurs during partitioning and final cooling. In case of high partitioning temperature cycles, austenite reverse transformation was observed. Certain cycles resulted in a very effective austenite stabilization and interesting microstructure.


2021 ◽  
Vol 1016 ◽  
pp. 1790-1796
Author(s):  
Maxim Syrtanov ◽  
Egor Kashkarov ◽  
Tatyana Murashkina ◽  
Nahum Travitzky

This paper describes the influence of sintering temperature on phase composition and microstructure of paper-derived Ti3AlC2 composites fabricated by spark plasma sintering. The composites were sintered at 100 MPa pressure in the temperature range of 1150-1350 °C. Phase composition and microstructure were analyzed by X-ray diffraction and scanning electron microscopy, respectively. The multiphase structure was observed in the sintered composites consisting of Ti3AlC2, Ti2AlC, TiC and Al2O3 phases. The decomposition of the Ti3AlC2 phase into Ti2AlC and TiC carbide phases was observed with temperature rise. The total content of Ti3AlC2 and Ti2AlC phases was reduced from 84.5 vol.% (1150 °C) to 69.5 vol.% (1350 °C). The density of composites affected by both the content of TiC phase and changes in porosity.


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