Dispersion-strengthened copper with was produced by ball-milling and spark plasma sintering (SPS).Ball-milling was performed at a rotation speed of 300rpm for 30 and 60min in Ar atmosphere by using a planetary ball mill (AGO-2). Spark-plasma sintering was carried out at for 5min under vacuum after mechanical alloying. The hardness of the specimens sintered using powder ball milled for 60min at 300rpm increased from 16.0 to 61.8 HRB than that of specimen using powder mixed with a turbular mixer, while the electrical conductivity varied from 93.40% to 83.34%IACS. In the case of milled powder, hardness increased as milling time increased, while the electrical conductivity decreased. On the other hand, hardness decreased with increasing sintering temperature, but the electrical conductiviey increased slightly

Cu- nanocomposite powders were synthesized by combining high-energy ball-milling of Cu-Ti-B mixtures and subsequent self-propagating high temperature synthesis (SHS). Cu-40wt.% powders were produced by SHS reaction and ball-milled. The milled SHS powder was mixed with Cu powders by ball milling to produce Cu-2.5wt.% composites. particles less than 250nm were formed in the copper matrix after SHS-reaction. The releative density, electrical conductivity and hardness of specimens sintered at were nearly 98%, 83%IACS and 71HRB, respectively. After heat treatment at 850 to for 2 hours under Ar atmosphere, hardness was descedned by 15%. Our Cu- composite showed good thermal stability at eleveated temperature.

Effects of sintering conditions such as sintering temperature and heating rate on oxygen content, density, microstructure and toughness of sintered Mo were investigated. The oxygen content of the sintered Mo significantly depended on the sintering conditions. The oxygen content of the primary sintered(below 1673 K) Mo influenced the densifications. The number of pores at grain boundaries of the secondary sintered(at 2073 K)Mo depended on the oxygen content of the primary sintered Mo. Grain growth of the secondary sintered Mo was inhibited by the existence of pores at the grain boundaries. The secondary sintered Mo having larger number of pore and smaller grain size demonstrated higher strength.

The kinetics of sintering of Co-Fe materials was studied. The main objective was to establish the effects of iron content and sintering parameters on the microstructure and phase composition of the as-sintered material. Specimens containing from 3 to 25 wt.% iron were sintered in a dilatometer for one hour at 900, 1000 and in either hydrogen or nitrogen atmosphere. The length of specimens during the heating, hold at temperature and cooling steps were monitored to establish the sample's shrinkage. Microstructural observations were carried out on polished and etched transverse sections which were also subjected to the X-ray phase analysis.

Several boride sintered bodies such as , , and were previously reported. In the present study, the sinterability and physical properties of chromium boride containing chromium carbide sintered bodies were investigated in order to determine its new advanced material. The samples were sintered at desired temperature for 1 hour in vacuum under a pressure by hot pressing. The relative density of sintered bodies was measured by Archimedes' method. The relative densities of addition of 0, 5, 10, 15 and 20 mass% composites were 92 to 95%. The Vickers hardness of the with 10 and 15 mass% composites were about 14 and 15 GPa at room temperature, respectively. The Vickers hardness at high temperature of the addition of 10 mass% composite decreased with increasing measurement temperature. The Vickers hardness at 1273 K of the sample was 6 GPa. The Vickers hardness of addition of composites was higher than monolithic sintered body. The powder X-ray diffraction analysis detected CrB and phases in containing composites.

The Powder characteristics and sintering behavior of coated were studied. Silica coated powders were prepared by sol-gel method. The particle size of the powders were nm and the thickness of the coating layer was nm. As the content increased, the layers improved the powder dispersion. The Zeta potential of coated was getting close to that of pure silica with a more negative charge, compared with that of the uncoated . The onset temperature of shrinkage curves shifted to higher temperatures with increasing contents

Carbon nanotube (CNT) reinforced hydroxyapatite (HAp) composites were fabricated by using the spark plasma sintering process with surfactant modified CNT and HAp nano powder. Without the dependency on sintering temperature, the main crystal phase existed with the HAp phase although a few contents of (Tri calcium phosphate) phase were detected. The maximum fracture toughness, was obtained in the sample sintered at and on the fracture surface a typical intergranular fracture mode, as well as the pull-out pmhenomenon of CNT, was observed.

In this study, hydroxyapatite (HAp) and hydroxyapatite-yttria stabilized zirconia (HAp-3YSZ) with 20 vol. %– (ZrO2+3 %mol Y2O3) nanopowders were consolidated very rapidly to full density by High-frequency induction heat sintering (HFIHS). Effects of temperature and the addition of 3YSZ on the toughness, hardness and microstructure properties have been studied. 3YSZ second phase toughening HAp composites with higher toughness were successfully developed at relatively low temperatures through this technique. Compared with hardness and toughness obtained for pure HAp, the hardness and toughness for HAp-20vol. % 3YSZ were much higher.

The HTCC based multilayer structure plasma head unit have some difficulties in fabrication due to complicated post-processes, such as heat treatment at reduced atmosphere, re-bonding of each layer, and silver metallization. On the other hand, LTCC based technology provides relatively simple process for multilayer plasma unit except weak mechanical properties. To overcome this problem a combined scheme using both LTCC and HTCC technology has been developed in our group, recently. In this work, we report the structural design, materials selection, joining of LTCC with HTCC substrate, and co-firing process for the fabrication of multilayered atmospheric plasma head unit.

WC-10Co-0.8VC nanocrystalline powders were sintered by spark plasma sintering (SPS) and hot press sintering (HPS), and the microstructure and properties were compared. Results show that dense WC-10Co-0.8VC can be obtained by SPS in several minutes when the sintering temperature is >1200℃. Sintered at a temperature of 1300℃, the sample prepared by SPS for 3 minutes has higher density, finer grains and better properties than that prepared by HPS for 60 minutes. SPS can be used to prepare nanocrystalline WC-10Co-0.8VC with improved properties when suitable sintering parametesr are chosen.

Sintering behavior of the Fe-0.8Mn-0.5C powder system was studied on the specimens with a density of ~7.0 g/cc sintered at 11200C for 30 min in a gas mixture of 7%H2/93%N2 with the inlet dew point of -600C. During the atmosphere monitoring (CO/CO2-content and dew point) was showed, that carbothermical reduction occurs in two different temperature ranges; three peaks of dew point profile also can be distinguished during sintering cycle as well. Following sintering the Mn-content distribution and microstructures around the Mn-source were micro-analytical evaluated; the results showed that manganese travels through porous iron matrix up to ~60 μm.

The compaction and sintering behavior of zirconium titanate (ZrTiO4) was investigated by means of the measurement of sintering density and shrinkage, and the observation of microstructure. With increasing the content of Al2O3 additive, Al2O3-modified zirconium titanate samples fired at 1300oC showed the anisotropic shrinkage behavior that the upper region of sintered body has higher sintering shrinkage than the low region. This difference of sintering shrinkage decreased with increasing firing temperature from 1300 to 1400oC. The SEM micrographs of powder compation show that the anisotropic shrinkage behavior is related with non-uniform density in a uniaxial compaction.

Hydrogen, in even small quantities, is extremely deleterious to the sintering of aluminium. Understanding the cause of this effect is complicated by the multiple interactions that occur in multi-component systems. In this work, we examine the sintering rsponse of Al-2Mg (a simplified system) in pure nitrogen and nitrogen-hydrogen using dilatometry, differential scanning calorimetery, thermogravimetry and metallography.

The removal of oxygen during sintering by carbothermic reduction was studied for steel compacts Fe-Cr-Mo-C and Fe-Mo-C prepared from prealloyed powders. The compacts were prepared by pressing at 600 and 1000 MPa and sintering at 1100 and 1300°C in vacuum. It showed that for the Cr-Mo steel, deoxidation strongly depends on the sintering temperature, in contrast to the plain Mo steel; at 1300°C very low oxygen levels were measured with the standard density compact while at high density still significant oxygen is contained. This indicates inhibition of final deoxidation by pore closure, but apparently without adverse effect on the mechanical properties.

Pulsed Current Sintering (PCS) process possesses some problems that need to be resolved. We, therefore aims at understanding phenomena of PCS process by presenting some basic data on in situ sintering behavior of PCS. Special graphite mold equipped with thermo couple and electrodes were designed to measure the temperature, electric current and voltage inside the powder during PCS process. We apply three types of raw materials, especially for ZnO as semiconductor, Al2O3 as non-conductor and WC as good conductor. The electric current and voltage were measured for each powder during PCS process. In addition, their electric resistance properties were calculated.