Erosion-corrosion resistant nitride cermets
A cermet, nitride technology, applied in the field of cermet
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Embodiment 1
[0036] 70vol% of 2-5μm average diameter TiN powder (99.8% purity, obtained from Alfa AeSaR) and 30vol% of 6.7μm average diameter 304SS powder (OSPRey metal, 95.9% sieve-16μm) were dispersed in low-pressure polyethylene with ethanol in a grinding container. The powder in ethanol was mixed with yttria-toughened zirconia pellets (YZT) (10 mm diameter, obtained from Tosoh Ceramics) in a ball mill at 100 rpm for 24 hours. Ethanol was removed from the mixed powder by heating at 130° C. in a vacuum oven for 24 hours. The dry powder was compacted in a 40 mm diameter die in a hydraulic coaxial press (SPEX 3630 Automated X-press) at a pressure of 5,000 psi. The resulting green disc was ramped at 25°C / min to 400°C under argon and held for 30 minutes to remove residual solvent. The wafer was then heated to 1500°C at 15°C / min in argon and held at 1500°C for 2 hours. Then the temperature was reduced to below 100°C at -15°C / min.
[0037] The resulting cermet contains:
[0038] i) 69 vol...
Embodiment 2
[0042] As described in Example 1, 70 vol% of CrN powder (99.8% purity, obtained from AlfaAesar, 99% sieve 325 mesh) and 30 vol% of 304SS powder with an average diameter of 6.7 μm (Osprey metal, 95.9% sieve -16 μm) for processing the cermet disc. The cermet disc was then heated to 1450°C at 15°C / min in argon and held at 1450°C for 2 hours. Then the temperature was reduced to below 100°C at -15°C / min.
[0043] The resulting cermet contains:
[0044] i) 20 vol% CrN with an average particle size of about 25 μm
[0045] ii) 50 vol% of the second nitride M having an average particle size of about 1 μm 2 N, where M = Cr, Fe, Ni
[0046] iii) 30vol% Cr-poor alloy binder.
[0047] figure 2 is a scanning electron microscope image of a CrN cermet processed according to this example, where the scale bar represents 50 μm. In this image, the CrN phase appears dark and the binder phase appears light. The Cr-rich second M 2 The N phase is likewise shown in the binder phase.
Embodiment 3
[0049] Each of the cermets of Examples 1 and 2 was subjected to the Thermal Abrasion and Abrasion Test (HEAT). The steps used are as follows:
[0050] 1) Weigh a cermet disc sample with a diameter of about 35 mm and a thickness of about 5 mm.
[0051] 2) The center of one side of the wafer is then subjected to 1200 g / min of SiC particles (220 abrasive, #1 grade black corundum, UK grinding) entrained in hot air leaving a 0.5 inch diameter tube at an angle of 45 degrees agent, Northbrook, IL) treatment was terminated at 1 inch from the target. The speed of SiC is 45.7 m / s.
[0052] 3) Step (2) was carried out at 732° C. for 7 hours.
[0053] 4) After 7 hours, the samples were cooled to ambient temperature and weighed to determine weight loss.
[0054] 5) Determine the wear of a commercially available castable alumina refractory sample for use as a reference standard. The reference standard wear was given a value of 1 and the results are listed in Table 1 for the cermet samp...
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