The Effects of Austempering Temperature and Time on Mechanical Properties of Ductile Cast Iron Grade FCD450

2020 ◽  
Vol 856 ◽  
pp. 92-98
Author(s):  
Janthira Chantarach ◽  
Rungsinee Canyook

The purpose of the study was to inspect microstructure, mechanical properties and impact toughness of ductile cast iron grade FCD450 produced by austempering process. The study focused on austempering parameter, which effected impact toughness of material at low temperature. The FCD450 was initially temperature austenized at 885°C (1625˚F) for 2 hours. Austempering was carried out at three different temperatures of 271°C (520˚F), 313°C (560˚F) and 357°C (675˚F). The austempering temperature were varied at 1.5, 2.5 and 3.5 hours. X-ray diffraction was showed that the austempered ductile cast iron (ADI) microstructure consists of austenite and ferrite. The results showed that when austempered at 357°C (675˚F) for 2.5 hours has highest hardness and impact energy at low temperature. The dimple ductile fracture of ADI fracture surfaces was revealed by scanning electron microscope (SEM).

1989 ◽  
Vol 179 ◽  
Author(s):  
M. R. Silsbee ◽  
R. A. Steinke ◽  
D. M. Roy ◽  
D. K. Agrawal ◽  
R. Roy

AbstractReactive aluminas, including rapidly calcined gibbsites, offer exciting potential for forming ceramic materials at low temperatures. New x-ray amorphous aluminas will react with water at room temperatures to form compacts with 10–50 MPa tensile strengths, via viscous slurries. The cementious behavior of these materials has been examined. The results of TGA, x-ray diffraction, SEM, mechanical properties, and other characterization techniques, as applied to these systems, will be discussed.


2013 ◽  
Vol 744 ◽  
pp. 349-352
Author(s):  
Xiao Hu ◽  
Xiang Chen ◽  
Yan Xiang Li

A kind of austempered boron alloyed high silicon cast alloy was developed though modification with Ti and controlling austempering temperature, the impact toughness of which increases to 20.7 J/cm2, which is more than triple that of the previous work. The alloy with modification exhibits obvious grain refining both in matrix and boride, improved the morphology of boride into discontinuous network and small particles. The phenomenon and mechanism are discussed in the article, it proved TiC is possible to act as the nuclei of eutectic boride and Ti can be an effective modifier.


2013 ◽  
Vol 744 ◽  
pp. 357-361
Author(s):  
Yun Long Ai ◽  
Qing Long ◽  
Wei Hua Chen ◽  
Bing Liang Liang

Effect of RE and V on microstructure and mechanical properties of high chromium cast iron were investigated by optical microscopy, scanning electron microscopy, X-ray diffraction, impact test and wear test. The results show that proper modification using RE combined with V makes the alloy present a more refined and homogenous austenite matrix, and makes the morphology of carbide changing from thick lath to thin lath, and rosette-like. Modification can also increase hardness, wear resistance and impact toughness of high chromium cast iron.


2014 ◽  
Vol 602-603 ◽  
pp. 130-133 ◽  
Author(s):  
Zheng Yang Li ◽  
Li Bo Wang ◽  
Guo Cai Zhong ◽  
Sai Sai Li ◽  
Ai Guo Zhou

Titanium tin carbide (Ti2SnC) is a member a MAX phases, which are ternary carbides or nitrides with layered structure. Ti powders are normally used as Ti source to synthesize Ti2SnC. In this paper, TiH2, a relative cheaper Ti source, was used to synthesize Ti2SnC. Ti2SnC was synthesized from TiH2/Sn/TiC or TiH2/Sn/graphite powders by a tube furnace at different temperatures under Ar atmosphere. From the analysis of X-ray diffraction results, the lowest temperature to synthesize Ti2SnC was 1000 °C. Ti2SnC content increased with temperature, and high purity Ti2SnC was fabricated at 1200 °C. From scanning electron microscopy, as-synthesized Ti2SnC from TiH2/Sn/TiC was with plate-like structure. However, for Ti2SnC from graphite as carbon source, there was some stripe microstructure. Some large pores existed between the Ti2SnC particles. The existence of the pores make the mechanical properties of Ti2SnC block significantly reduced, its compressive strength was only 0.483 MPa or 0.35 MPa respectively for samples synthesized from TiC or graphite as carbon source. The low mechanical properties make the porous sample easy to be broken as powders.


1982 ◽  
Vol 26 ◽  
pp. 291-298 ◽  
Author(s):  
Zenjiro Yajima ◽  
Yukio Hirose ◽  
Keisuke Tanaka

X-ray diffraction observation of metal fractures provides fracture analysists with useful information on the mechanisms and mechanical conditions of fracturing. This method is called “X-ray fractography” and has been developed especially in Japan as a new engineering tool for fracture analysis.In the present paper, X-ray fractography is applied to fracture surfaces of ductile cast iron (JIS FCD 60) which are widely used as machine parts. The fracture toughness tests were conducted at ambient and low temperatures by using compact tension (CT) specimens with blunt notches and three-point bending (TPB) specimens with fatigue pre-cracks. The line broadening of X-ray diffraction profiles was measured on and beneath fracture surfaces of fracture toughness specimens.


1941 ◽  
Vol 14 (3) ◽  
pp. 544-545 ◽  
Author(s):  
Norman Bekkedahl ◽  
Lawrence A. Wood

Abstract Data presented in this communication show an instance in which melting of a crystalline material is very much dependent on the temperature at which the crystals have been formed. It is well known that many substances in which crystallization is relatively slow can be crystallized at different temperatures in a range below the melting point, but no effect of the crystallization temperature on the temperature of melting seems to have been previously reported. The quantitative results for crystalline rubber, the material under investigation, are shown in Figure 1. The crystallization of unvulcanized rubber in the unstretched state has been found to occur at temperatures between about −40° C and 13° C. The time required for crystallization is about one year at 13° C, about ten days at 0° C, and a few hours at −20° C. Below −40° C the mobility is presumably insufficient for the formation of crystals. Crystallization and fusion are accompanied by changes in volume, heat capacity, light absorption, birefringence, x-ray diffraction, and mechanical properties such as hardness. The volume decreases about 2.5 per cent on crystallization, and the magnitude of the change is little influenced, if at all, by the temperature. Fusion, as measured by the volume increase, is found to be independent of the rate of heating, and to occur over a range of five or ten degrees.


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