A DTA Study on HVOF Thermally Sprayed WC–M Coatings

2007 ◽  
Vol 566 ◽  
pp. 155-160
Author(s):  
M. Heydarzadeh Sohi ◽  
Shahin Khameneh Asl ◽  
Kazuyuki Hokamoto ◽  
M. Rezvani

Five types of tungsten carbide based powders with different chemical compositions (WC-12Co, WC-17Co, WC-10Ni, WC-10Co-4Cr and WC- 20Cr-7Ni) were deposited onto ST37 mild steel substrate using high velocity oxy fuel (HVOF) spray technique. The feedstock powders and sprayed coatings were studied by using X-ray diffraction (XRD), and differential thermal analyzing (DTA). The results were shown during HVOF thermal spraying, WC-M powders become partially melted before being sprayed on the surface of the substrate with supersonic speed. In these types of coatings, the crystallographic structures are normally non equilibrium, because the cooling rates of the deposited splats are very high due to the cold substrate acting as a thermal sink. These partially melted powders are then rapidly solidified to an amorphous phase. XRD analysis showed that the amorphous phase was existed in all of the as sprayed coatings. The amorphous phase in WC-12Co, WC-17Co and WC-10Ni coatings was transformed to crystalline phases by heat treatment at high temperature. Heat treatment of these coatings at high temperature also resulted in partially dissolution of WC particles and formation of new crystalline phases. In cobalt base coatings, the new phases were eta carbide phases like Co6W6C and Co3W3C but in WC-10Ni coating a NiW intermetallic phase was formed. Heat treatment of WC-10Co-4Cr and WC-20Cr-7Ni coatings did not change the amorphous phases in these coatings. Differential thermal analysis of cobalt containing coatings revealed an exothermic reaction at approximately 880°C. This exothermic reaction may be related to the transformation of the amorphous phase to eta phases. On the contrary, DTA analysis of feedstock powders of these coatings showed an endothermic reaction at approximately 1000°C. DTA analyses of nickel containing cermets also showed similar results. Differential thermal analysis of chromium containing cermets did not show any noticeable exothermic or endothermic reactions.

2010 ◽  
Vol 158 ◽  
pp. 52-55 ◽  
Author(s):  
Ye Han ◽  
Ming Gu ◽  
Wei Wei Zhang ◽  
Shu Yu Yao

The Fe2O3-CaO-SiO2 glass ceramics were prepared by the method of quenching and controlled crystallisation. Differential thermal analysis, X-ray diffractometry and vibrating sample magnetometer were used to study the crystallisation and magnetic properties of Fe2O3-CaO-SiO2 glass ceramics. It was concluded that the main crystalline phases of glass ceramics during the process were Hematite, Iron Silico Oxide and Hedenbergite. The saturation magnetisation values (Ms) of glass ceramics varied between 108 emu•g-1 and 147 emu•g-1. The crystallisation of Hedenbergite lead to the high Hc value (~2000Oe).


2011 ◽  
Vol 284-286 ◽  
pp. 1431-1434 ◽  
Author(s):  
Jin Rui Zhang ◽  
Ru Wang

In order to utilization the molybdenum tailings which be deposited in large quantities. Test used it to prepare glass-ceramics as main raw material, TiO2 as nucleation agents and CaO-Al2O3-SiO2 system and wollastonite as the principal crystalline phase. Heat treatment system of glass-ceramics was based on the differential thermal analysis. The crystalline phase, microstructure and characteristics of glass-ceramics were analysis by XRD, SEM and physical, chemical properties test. The result shows that the performance of glass-ceramics was superior to the other types of building decoration stone.


1964 ◽  
Vol 8 ◽  
pp. 78-85 ◽  
Author(s):  
P. K. Gantzel ◽  
S. Langer ◽  
N. L. Baldwin ◽  
F. L. Kester

AbstractThermal analyses of samples of thorium dicarbide in equilibrium with graphite show arrests which indicate phase transitions at 1427 ± 21°C arid 1481 ± 28°C. These thermal effects have been observed on heating and cooling both in standard thermal analysis and in differential thermal analysis using graphite as a reference material. The microstructure of thorium dicarbide samples shows the characteristic “herringbone” pattern of a material which has undergone a martensitic-type transition.A high-temperature X-ray investigation has revealed that the observed thermal arrests correspond to erystallographic transformations. The monodinic modification found at room temperature is stable to 1427°C, at which temperature a tetragonal modification with a0 = 4.235 ± 0.002Å and c0 = 5.408 ± 0.002Å is formed. At 1481°C, the tetragonal is transformed to cubic with a0 = 5.809 ± 0.002 Å. The best agreement between observed and calculated intensities has been obtained with C-C units of 1.5-Å assumed bond length in space groups P42/mmc and Pa3 for the tetragonal and cubic modifications, respectively.


1994 ◽  
Vol 30 (4) ◽  
pp. 435-439 ◽  
Author(s):  
A. Flores-Valdes ◽  
M.I. Pech-Canul ◽  
M. Méndez-Nonell ◽  
M. Sukiennik

1963 ◽  
Vol 36 (4) ◽  
pp. 1059-1070 ◽  
Author(s):  
M. L. Bhaumik ◽  
D. Banerjee ◽  
Anil K. Sircar

Abstract A method for the determination of the heat of the hard-rubber reaction by the application of differential thermal analysis is reported. The heat of reaction was determined with stocks containing different rubber/sulfur ratios and also with a 68/32 stock, preheated to contain different amounts of combined sulfur. Heat evolution is observed first with samples containing about 7 per cent sulfur and therefrom the amount of heat evolved shows a nearly linear increase up to 30 per cent sulfur. With increasing combined sulfur in the 68/32 stock, the quantity of exothermic heat gradually diminishes; so also does the temperature of initiation, i.e., the temperature at which heat evolution appears to begin. Initiation of the exothermic reaction appears to be a function of composition and temperature of the mass. An increase in the rate of reaction was observed when the composition reached 0.5 g-atom of sulfur per isoprene unit. An endothermic dehydrogenation reaction is observed at the end of the hard-rubber reaction. This, however, does not affect the determination of exothermic heat, because there is similar dehydrogenation taking place in the reference material (ebonite) which almost balances this heat loss. The final product has a lower sulfur content due to loss of sulfur as hydrogen sulfide.


2011 ◽  
Vol 673 ◽  
pp. 167-172 ◽  
Author(s):  
Shahin Khameneh Asl ◽  
Mohammad Reza Saghi Beyragh ◽  
Neda Faale Noori

The current study is focused on WC-Ni cermet coatings, materials that are extensively used in applications requiring wear resistance. In this work, WC-10%Ni powder was thermally sprayed onto mild steel using High Velocity Oxy Fuel (HVOF) spray technique. The nanostructured specimen was produced from sprayed samples by heat-treating at 1100°C in a vacuum chamber. Their structures were studied by using X-ray diffraction (XRD) and scanning electron microscopy (SEM). Polarization and electrochemical impedance spectroscopy (EIS) tests were performed on both types of coated samples in 3.5% NaCl solution. The amorphous phase in WC-10%Ni coating was transformed to crystalline phases by heat treatment at high temperatures. Heat treatment of these coatings at high temperature also resulted in partially dissolution of WC particles and formation of new crystalline phases. Generation of these phases produced the nanostructured coating with better mechanical properties. Comparative electro chemical test results showed that, the heat treatment could improve corrosion resistance of the nanostructured WC-10%Ni coating than the as sprayed coatings.


2017 ◽  
Vol 21 (2) ◽  
pp. 1067-1081 ◽  
Author(s):  
Dejan Radic ◽  
Miroslav Stanojevic ◽  
Marko Obradovic ◽  
Aleksandar Jovovic

High-temperature thermal process is a commercial way of regeneration of spent granular activated carbon. The paper presents results of thermal analysis conducted in order to examine high-temperature regeneration of spent activated carbon, produced from coconut shells, previously used in drinking water treatment. Results of performed thermogravimetric analysis, derivative thermogravimetric analysis, and differential thermal analysis, enabled a number of hypotheses to be made about different phases of activated carbon regeneration, values of characteristic parameters during particular process phases, as well as catalytic impact of inorganic materials on development of regeneration process. Samples of activated carbon were heated up to 1000?C in thermogravimetric analyser while maintaining adequate oxidizing or reducing conditions. Based on diagrams of thermal analysis for samples of spent activated carbon, temperature intervals of the first intense mass change phase (180-215?C), maximum of exothermic processes (400-450?C), beginning of the second intense mass change phase (635-700?C), and maximum endothermic processes (800-815?C) were deter-mined. Analysing and comparing the diagrams of thermal analysis for new, previously regenerated and spent activated carbon, hypothesis about physical and chemical transformations of organic and inorganic adsorbate in spent activated carbon are given. Transformation of an organic adsorbate in the pores of activated carbon, results in loss of mass and an exothermic reaction with oxygen in the vapour phase. The reactions of inorganic adsorbate also result the loss of mass of activated carbon during its heating and endothermic reactions of their degradation at high temperatures.


Sign in / Sign up

Export Citation Format

Share Document