Bar Grate
Bar Grate
Bar Grate
29
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1
The School of Material Science and Engineering, Henan Polytechnic University, Jiaozuo 454000 China;
2
Zhongyuan Special Steel Co., LTD, Jiyuan 454150, China
∗
Corresponding author. Tel.: 0086-391-3987472;
E-mail address: xulei_80@126.com
30 C. Zhiru, X. Lei et al.: The casting process and high...
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machining. To prolong the working life of the bar, and φ40 mm. The pouring temperature is controlled
casting process was simulated to eliminate the to be 1570°C.
defects using View-cast software, and effect factors
of high temperature oxidation were also discussed.
The simulation prediction of defects distribution in the metal content is above 95% and that these parts
the castings solidified is completely illustrated in are deemed as non-defective. It can also be found
Fig. 4. The transparency in the figure indicates that that large scale of shrinkages exists in the ingrate
32 C. Zhiru, X. Lei et al.: The casting process and high...
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and sprue cup, while none in the casting. Therefore, 3 High temperature oxidation resistance of
the designed casting process is suitable for the bar
manufacture of the grate bar. Fig. 5 shows the grate
bar produced by the designed casting process. It can 3.1 High temperature oxidation test method
be observed that surface smoothness of the casting
is excellent. While sintering machine is working, the grate bars
are in the alternating hot and cold working
environment. The bar may be heated to the
temperature in range of 700°C to 900°C, which
requires well high temperature oxidation resistance.
Thus, the temperature of high temperature oxidation
test was set between 700°C and 900°C.
Before the test, samples cut from the bar were
firstly ground into the size of 4 mm × l0 mm × 20
mm. All samples were cleaned by ultrasonic with
acetone solution and anhydrous ethanol orderly.
Then these samples were divided into 8 groups, and
each group had three samples. Second, the crucible
roasted for 1 hour at 150°C for holding samples.
The crucible and the sample were numbered
Figure 4. The simulation forecast map of defects in together and weighted using an analytical balance
grate bar. with the accuracy of 0.0001 g. At last, the crucible
containing a sample was put into a furnace to be
tested. Four groups were respectively heated to
600°C, 700°C, 800°C and 900°C, inside a high
temperature resistance furnace protected by argon
gas, while the other four without the protected gas.
After being kept for 5 hours, the crucibles were
taken out and were air cooled to room temperature.
Again the crucibles with the sample were weighted
together.
According to the national standard (GB/T 13303-
91), the oxidation rate would be calculated as the
following formula.
ml − mo
K= (1)
so · t
3.2 The analysis of high temperature oxidation Moreover, chromium content of the experimental
resistance grate bar was very high, Cr atoms would also
combine with oxygen atoms, then Cr2O3 oxide film
It is obvious to see from Table 2 and Figure 6 that formed. Cr2O3 oxide film firmly combined with the
the weight gain on per square meter at per hour is casting and prevented the diffusion of oxygen atoms.
0.67076 g after being kept at 600°C for 6 h and Furthermore, Cr element raised the formation
cooled to room temperature without argon temperature of FeO. As a result, the oxidation
protection. When the temperature was raised to resistance temperature was promoted. By the
700°C, the oxidation rate is slightly decreased to be corporate protection of Fe3O4, Fe2O3, Cr2O3 films,
0.56127 g/m2•h. When the test temperature reached the sample had well oxidation resistance at
800°C, oxidation rate is 0.90679 g/m2•h, which is temperature in range of 600°C to 800°C, without
about 35% higher than that at 600°C. The oxidation protected argon gas. The oxidation rate of the
rate is sharply increased to be 3.45811 g/m2•h, about sample was delayed to be only about 0.56127
5 times of that at 600°C, with raising the test g/m2•h to 0.90679 g/m2•h, as shown in Fig. 6.
temperature to 900°C. SEM was used to investigate the oxide film formed
At high temperature, iron is easily oxidized on the at 800°C, shown in Fig. 7. It can be observed that
surface of the sample. And the formation of FeO, the content of Cr sharply increases in the area where
Fe3O4 or Fe2O3 oxide is related to the temperature. the scanning distance is 1.6 μm, while the content of
Below the temperature of 560°C, the oxide film Fe is less. When the scanning distance reaches
mainly consists of Fe3O4 and Fe2O3, which have about 7.2 μm, the content of Cr decreases rapidly,
higher density and small lattice constant. The film while that of Fe increases sharply. It is obvious that
can prevent the diffusion of oxygen atoms and then a 5.6μm-thick oxidation layer exited between resin
delay the oxidation of iron. When the temperature is and matrix of the sample. Variations of the
over 560°C, FeO layer will be formed under the concentrations of Cr, Fe and O indicate that the
oxide films of Fe3O4 and Fe2O3. FeO layer has a outer and the inner layer of the oxide film were
simple lattice structure, which is the omission solid consisted of equivalent amount of iron oxide and
solution of iron atoms. It is easier for oxygen atoms chromium oxide. However, in the middle layer, the
to diffuse through FeO layer combining with iron film was mainly chromium oxide, considered as
atoms and aggravate iron oxidation [14]. Cr2O3, while that of the iron oxide was few. It is
thought that this kind of middle layer of the oxide
film is conductive to delay the diffusion of oxygen
and improve high temperature oxidation resistance
of the sample.
34 C. Zhiru, X. Lei et al.: The casting process and high...
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(a) (b)
Matrix
Resin
Oxide layer
Figure 7. Linear SEM-EDS scanning of the oxide layer formed on the sample tested at 800℃ without
protected gas.
The result of Linear SEM-EDS scanning of the forming element, it will dissolve in cementite to
oxide film formed at 900°C is shown in Fig. 8. It form alloy cementite with the sample heated at
can be seen that the thickness of the oxide film is 900°C. As a result, Cr2O3 membrane reduced and
about 11.5 μm (scanning distance from 1.5 μm to 13 broke gradually, then oxygen atoms diffused inside,
μm), much thicker than that formed at 800°C. It has leading to rapid oxidation and consequent
also been found that the concentration of iron is significant increase of the weight gain. When
about equal to that of chromium in the majority of oxidation temperature was high, the frequent
the oxide film, which reduces the compactness. In contact, collision, and friction between the grate bar
the inner layer close to the matrix, the concentration and sintering material result in the fast growth,
of iron is higher than that of chromium, which is abscission, and sprout of oxide film on the surface
considered to be mainly consist of FeO. This kind of the grate bar. At last, the grate bar breaks down.
of oxide film can not prevent the diffusion of In order to improve the service life of the grate bar,
oxygen, leading to severe oxidation of the bar. This working temperature must be controlled strictly.
phenomenon is analyzed to be caused by dissolution
of chromium. Since chromium is a strong carbide
Figure 8. Linear SEM-EDS scanning of the oxide layer formed on the sample tested at 900℃ protected by
argon gas.
Engineering Review, Vol. 39, Issue 1, 29-36, 2019. 35
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In the test, it has also been found that the weight argon gas. From the line scanning, about 1.8μm-
gain is lower by near an order of magnitude on thick oxide film containing much Cr can be
the sample protected by argon gas, compared with observed. The variations of concentrations Fe, Cr
the non-protected, shown in Fig. 6(b). Only when and O in the oxide film are similar as that in the
the test temperature was raised to 800°C, the film, formed at 900°C without the protected gas.
oxidation rate increased gradually. The oxidation Hence, it is apparent that the oxidation mainly
rate at 900°C increased substantially, similar to occurred in heating and insulation process, while
that at air atmosphere, and reached 0.69240 rarely existed in the cooling. The oxidation is
g/m2•h. Fig. 9 is the linear SEM-EDS scanning of notably affected by temperature and the
the oxide layer cross section under 900°C with consequent constitute of the oxide film.
Figure 9. Linear SEM-EDS scanning of the oxide layer formed on the sample tested at 900℃ without
protected gas.
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