Patent Grant
7276204
1. Field of the Invention
The present invention relates to carburization treatment methods for carburizing steel material and a carburization treatment apparatus suitable for carrying out the carburization treatment methods.
2. Description of the Related Art
Various methods are known for carburizing steel material, such as a gas carburization method, a vacuum carburization method, and a plasma carburization method, with each having both advantages and disadvantages.
However, one gas carburization method has a disadvantage of the generation of a large amount of CO2 gas and a possibility of an explosion. A further problem associated with this method is that intergranular oxidation will occur on the surface of the steel material. On the other hand, another gas carburization method using an endothermic gas makes it necessary to employ a metamorphism furnace, hence suffering from a problem of high equipment cost.
A vacuum carburization method is associated with a problem in that once the carbon concentration on the surface of a steel material is increased to a predetermined solid solubility, a large amount of soot will be undesirably generated. As a result, not only does the carburization equipment need a comparatively long time and a considerably high cost for maintenance, but also such equipment does not have sufficient versatility. Moreover, another problem associated with this method is that it is difficult to perform a carbon potential control in an atmosphere within the furnace, if compared with the above-described gas carburization methods. In addition, a plasma carburization method is said to be low in productivity.
Accordingly, it is an object of the present invention to provide improved, new and economical carburization treatment methods which can be effectively used to replace any one of the above-described conventional carburization methods. It is another object of the present invention to provide an improved carburization treatment apparatus which is suitable for carrying out the carburization treatment methods provided according to the present invention.
In order to achieve the above objects of the present invention, a carburization treatment method according to the present invention comprises performing the carburization treatment while supplying a hydrocarbon gas and an oxidative gas into a furnace kept at a reduced pressure.
With the use of the present invention, since it is possible to dispense with an exhaust gas burning process (which was needed in the above-described conventional gas carburization method), the CO2 gas generation amount can be reduced so as to reduce an explosion possibility. Further, since it is not necessary to employ a metamorphism furnace, the amount of gas necessary to be used in the carburization treatment can be reduced, thereby rendering the whole process of carburization treatment more economical. Moreover, different from the above-described vacuum carburization method, since the method of the invention makes it possible to supply not only the hydrocarbon gas but also an oxidative gas, and since it is possible to control the carbon potential of the atmosphere within the furnace, the generation of soot can be prevented, thereby rendering easier the maintenance of the furnace.
As a preferred embodiment of the present invention, the carburization treatment is conducted while supplying a hydrocarbon gas and an oxidative gas, and an inert gas is further supplied during the carburization treatment. With the use of this method, it is possible to increase the gas amount within the furnace, thereby making it possible to ensure a uniform temperature rise and thus a uniform carburization treatment.
Further, as another embodiment of the present invention, it is preferable that the internal pressure within the furnace is 0.1 to 101 kPa. In other words, if the internal pressure within the furnace is lower than 0.1 kPa, it is impossible to ensure a desired carburization capability. On the other hand, if the internal pressure within the furnace is larger than 101 kPa, since such an internal pressure is generally close to atmospheric pressure, a problem will be caused which is similar to that associated with the above-described conventional gas carburization method.
Furthermore, in the above-described method according to the present invention, the hydrocarbon gas may be at least one selected from the group consisting of C3H8, C3H6, C4H10, C2H2, C2H4, C2H6 and CH4, while the oxidative gas may be air, O2 gas or CO2 gas.
Moreover, in the method according to the present invention, a carbon potential of the atmosphere within the furnace is controlled by controlling the amount of at least one of the hydrocarbon gas and the oxidative gas. At this time, the amount of at least one of the hydrocarbon gas and the oxidative gas is controlled by carrying out at least one of the following measurements which include: measurement of CO gas partial pressure, measurement of CO gas concentration, measurement of CO2 gas partial pressure, measurement of CO2 gas concentration, measurement of O2 gas partial pressure, measurement of O2 gas concentration, measurement of H2 gas partial pressure, measurement of H2 gas concentration, measurement of CH4 gas partial pressure, measurement of CH4 gas concentration, measurement of H2O partial pressure, measurement of H2O concentration, and measurement of a dew point, all within the furnace.
On the other hand, a carburization treatment apparatus according to the present invention comprises a hydrocarbon gas supply unit for supplying a hydrocarbon gas into a furnace; an oxidative gas supply unit for supplying an oxidative gas into the furnace; and a vacuum pump for reducing the internal pressure within the furnace. With the use of the carburization treatment apparatus according to the present invention, it is possible to carry out the above-described method of the present invention with a high efficiency. In contrast, a conventional gas carburization furnace is not associated with the use of a vacuum pump, and a conventional vacuum carburization furnace does not contain an oxidative gas supply unit since it is not needed.
The above carburization treatment apparatus further comprises an in-furnace atmosphere analyser for analysing the atmosphere within the furnace, and a pressure gauge to control the internal pressure within the furnace. With the use of such a carburization treatment apparatus, it is possible to correctly control the atmosphere within the furnace, and also to control and thus reduce the internal pressure within the furnace, thereby rendering it possible to more effectively carry out the above-described method of the present invention.
In addition, the above-described carburization treatment apparatus further comprises a computing device for computing a carbon potential in accordance with an analysis value fed from the in-furnace atmosphere analyzer, a regulation device for regulating the amount of at least one of the hydrocarbon gas and the oxidative gas in accordance with the computed values fed from the computing device, and a thermo-couple for controlling the internal temperature within the furnace. With the use of this carburization treatment apparatus, it is possible to automatically supply the hydrocarbon gas and/or the oxidative gas into the furnace, and it is also possible to control the internal temperature of the furnace.
Moreover, in the above-described carburization treatment apparatus, the in-furnace atmosphere analyzer is at least one of the following gauges and meters including CO gas partial pressure gauge, CO gas concentration meter, CO2 gas partial pressure gauge, CO2 gas concentration meter, O2 gas partial pressure gauge, O2 gas concentration meter, H2 gas partial pressure gauge, H2 gas concentration meter, CH4 gas partial pressure gauge, CH4 gas concentration meter and dew point hygrometer.
Referring to
With regard to the aforementioned carburization furnace having the above-described construction, the pressure reduction adjustment within the furnace can be carried out by controlling the discharge of an atmosphere from the furnace, by virtue of the pressure gauge 6 and the vacuum pump 12. Further, the carbon potential of an atmosphere within the furnace may be controlled in a manner described as follows, so that it is possible to maintain a high carbon potential which is slightly below a carbon solid solubility. At this time, the analysis values fed from the internal atmosphere analyzers 8, 9 and 30 are introduced into the carbon potential computing device 13. Then, the adjustment gauge 14, in accordance with the computed values provided by the carbon potential computing device 13, operates to send an adjustment signal to the mass flow controller 10 (for controlling the hydrocarbon gas supply amount) as well as to the mass flow controller 11 (for controlling the oxidative gas supply amount). In this way, it is possible to adjust an amount of at least one of the hydrocarbon gas and the oxidative gas being supplied into the furnace, thereby effectively controlling the carbon potential of an atmosphere within the furnace.
The control of an amount of the hydrocarbon gas and/or the oxidative gas being supplied into the furnace may be effected by measuring the partial pressure of at least one of various kinds of gases forming an atmosphere within the furnace. However, it is also possible to perform the same control by measuring the concentration of at least one of various kinds of gases forming the atmosphere within the furnace. For example, it is possible to measure the partial pressure or the concentration of at least one of CO gas, CO2 gas, O2 gas, H2 gas and CH4 gas (together forming an atmosphere within the furnace), by utilizing various partial pressure gauges (CO gas partial pressure gauge, CO2 gas partial pressure gauge, O2 gas partial pressure gauge, H2 gas partial pressure gas and CH4 gas partial pressure gas) or various concentration meters (CO gas concentration meter, CO2 gas concentration meter, O2 gas concentration meter, H2 gas concentration meter and CH4 gas concentration meter), thereby effecting correct control of the supply amount of the hydrocarbon gas and/or the oxidative gas when being supplied into the furnace.
Furthermore, it is possible to control an amount of the hydrocarbon gas and/or the oxidative gas being supplied into the furnace, by measuring the partial pressure of H2O or the concentration of H2O within the furnace, or by measuring the dew point of an atmosphere gas within the furnace using a dew point hygrometer.
In this way, with the use of the various methods as described in the above, it is possible to correctly control an amount of the hydrocarbon gas and/or the oxidative gas being supplied into the furnace, thereby making it possible to keep an atmosphere within the furnace at a high carbon potential which is slightly below the carbon solid solubility.
Referring to
An initial state of the carburization quenching apparatus will be described as follows. Namely, the inlet door 15, the outlet door 20 and the partition doors 21a, 21b and 21c are all closed. The carburization room 17 is heated to a quenching temperature and then kept at this temperature, while the pressure within the carburization room is controlled at 0.1 kPa or lower. Similarly, the pressure within the quenching room 19 is also kept at 0.1 kPa or lower, while the quenching oil within the quenching room 19 is heated to a temperature suitable for steel material quenching treatment. At this time, the transportation room 16 is under atmospheric pressure.
Starting from the above-described initial state, at first, the inlet door 15 is opened so that steel material is introduced into the transportation room 16. Then, the inlet door 15 is closed and the pressure within the transportation room 16 is reduced to 0.1 kPa or lower. Subsequently, the partition door 21a located between the transportation room 16 and the carburization room 17 is opened so that the steel material is moved to the carburization room 17. Then, the partition wall 21 is closed. On the other hand, although not shown in the drawings, an apparatus for transporting the steel material may be a chain device (for use in the transportation room 16 as well as in the oil quenching room 19 and driven by a motor, and may also be a roller hearth for use in the carburization room 17).
Then, after the partition door 21a is closed, the pressure within the carburization room 17 recovers to a predetermined pressure such as 100 kPa by virtue of N2 gas, while the temperature within the carburization room is elevated to the carburization temperature. Subsequently, after the carburization room has been kept at the carburization temperature for 30 minutes, N2 gas is discharged from the carburization room 17, so that the pressure within the carburization room 17 is reduced to 0.1 kPa or lower.
Afterwards, a predetermined amount of hydrocarbon gas and a predetermined amount of oxidative gas are supplied to the carburization room 17 by way of a purge line, so that an internal pressure within the carburization room 17 is allowed to be restored to its carburization pressure. Upon pressure restoration and based on the computation result obtained by processing the data representing the measured CO2 partial pressure or CO2 concentration, the carburization room 17 is allowed to control, with the use of a control line, the supply amount of at least one of the hydrocarbon gas and the oxidative gas. However, at this time, the carbon potential is set with reference to a carbon solid solubility which depends on a carburization temperature, so that such a carbon potential will be within a predetermined range so as not to produce soot.
After having performed the carburization treatment for a predetermined time period, the supply of the hydrocarbon gas as well as the oxidative gas to the carburization room 17 is stopped, and the atmosphere within the carburization room 17 is discharged so as to have the steel material kept under a reduced pressure, thereby adjusting the carbon concentration on the surface of the steel material. Then, the temperature within the carburization room 17 is lowered to the quenching temperature, and the partition door 21a is opened. Further, the partition door 21c located between the transportation room 16 and the quenching room 19 is opened, so that the steel material is transferred, under a reduced pressure, to the quenching room 19 by way of the transportation room 16, thereby performing an oil quenching treatment. After the quenching treatment, the steel material is taken out of the treatment system by way of the outlet door 20. At this moment, an adjustment of the carbon concentration on the surface of the steel material is allowed to be performed, and at the same time a control of the quenching temperature is carried out.
Furthermore, in the case of a high temperature carburization treatment (1050° C.) which requires an adjustment of crystal particles, after an adjustment has been performed on the carbon concentration on the surface of the treated steel material, the steel material is transported to the gas cooling room 18 by way of the transportation room 16 as well as the partition door 21b. Then, after the pressure has been restored to a predetermined value (for example, 100 kPa) by means of N2 gas, the steel material is cooled and the N2 gas is discharged, so that the pressure over the steel material is reduced to 1 kPa or lower. In this way, under a reduced pressure and by way of the transportation room 16, the steel material is returned to the carburization room 17 so as to be heated again to a temperature suitable for a reheating treatment. Moreover, the carburization room 17 is kept at the reheating temperature for 30 minutes. Then, the N2 gas is discharged so that the pressure within the carburization room is reduced to 1 kPa or lower. Subsequently, the steel material is transported to the quenching room 19 by way of the transportation room 16, thereby performing an oil quenching treatment. In this way, after the quenching treatment has been finished, the steel material is taken out of the treatment system by way of the outlet door 20.
In fact, the inventors of the present invention have conducted the carburization treatment using the method of the present invention, with an actual process and results thereof being discussed in the following.
Sections of steel material SCM 420 in the form of test pieces each having a diameter of 20 mm and a length of 40 mm were disposed at nine positions (upper and lower corner portions as well as in the central area) within the carburization room 17 whose internal temperature was controlled at 950° C. and whose internal pressure was controlled at 0.1 kPa or lower. Then, the pressure within the carburization room 17 was restored to 100 kPa by charging the room with N2 gas, while the internal temperature thereof was kept at 950° C.
After the carburization room 17 had been kept under the above-described conditions for 30 minutes, its internal pressure was reduced to 0.1 kPa by virtue of gas discharge. Subsequently, C3H8 gas and CO2 gas were supplied into the carburization room 17, each at a flow rate of 3.5 L/min so as to increase the internal pressure to 1.7 kPa.
Next, with the internal pressure of the carburization room 17 kept at 1.7 kPa, the amount of C3H8 gas and/or CO2 gas being supplied to the carburization room was changed so as to control the carbon potential to 1.25%. Then, the interior of the carburization room 17 was kept at 950° C. for 57 minutes.
Subsequently, the supply of C3H8 gas and/or CO2 gas was stopped and the internal pressure within the carburization room 17 was reduced to 0.1 kPa by virtue of gas discharge. Then, this internal pressure was kept for 37 minutes, while the internal temperature of the carburization room 17 was lowered to 870° C. during a subsequent time period of 30 minutes. Then, the steel material was transported to the quenching room 19 by way of the transportation room 16, thereby starting the oil quenching treatment.
The average carbon concentration distribution of the steel material treated in this example is shown in
When a carburization lead time of the carburization treatment in Example 1 was compared with a carburization lead time of the gas carburization treatment (which is a conventional process) using an endothermic gas, it was found that the conventional gas carburization treatment using an endothermic gas needed 118 minutes as its carburization lead time, while the carburization lead time of the carburization treatment in Example 1 was only 94 minutes, thus making it possible to shorten the carburization lead time by about 20%. In this way, using the carburization treatment method actually carried out in Example 1, it becomes possible to obtain a carburized layer having a desired depth using a shorter time period than required by the above described conventional gas carburization treatment (which requires the use of an endothermic gas). Therefore, the total energy consumption can be reduced and thus the desired economic advantage can be achieved. Moreover, since there is no soot being generated, the pieces of steel material can be placed at any position within the furnace without any limitation. In addition, the use of the present invention makes it possible to obtain carburized layers which are relatively uniform and differ little from each other in their physical and chemical properties.
Example 2 is used to explain how a high temperature carburization can be carried out. Namely, sections of steel material pieces which were identical to those used in Example 1 were disposed at nine positions within the carburization room 17 whose internal temperature was controlled at 1050° C. and whose internal pressure was controlled at 0.1 kPa or lower. Then, the pressure within the carburization room 17 was restored to 100 kPa by charging the room with N2 gas, while the internal temperature thereof was kept at 1050° C.
After the carburization room 17 had been kept under the above-described conditions for 30 minutes, its internal pressure was reduced to 0.1 kPa by virtue of gas discharge.
Subsequently, C3H8 gas and CO2 gas were supplied into the carburization room 17 at a flow rate of 14 L/min so as to increase the internal pressure to 1.7 kPa.
Next, with the internal pressure of the carburization room 17 kept at 1.7 kPa, the supply amount of CO2 gas was controlled at a constant flow rate of 10 L/min, while the supply amount of C3H8 gas was changed so as to have the carbon potential controlled at 1.4%. Then, the interior of the carburization room 17 was kept at 1050° C. for 16 minutes.
Subsequently, the supply of C3H8 gas and CO2 gas was stopped and the internal pressure within the carburization room 17 was reduced to 0.1 kPa by virtue of gas discharge. This internal pressure was kept for 16 minutes. Afterwards, the steel material was cooled and then heated again so as to adjust the size of the crystal particles.
In more detail, the steel material was transported from the carburization room 17 to the gas cooling room 18 by way of the transportation room 16. Then, the interior of the gas cooling room 18 was restored to 100 kPa by charging the room with N2 gas, followed by cooling the same for 15 minutes. Afterwards, the N2 gas was discharged and the internal pressure within the gas cooling room 18 was reduced to 0.1 kPa or lower. At this time, the steel material was transported into the carburization room 17 by way of the transportation room 16. Then, the steel material was heated so as to increase its temperature, with the heating process being conducted under a condition in which the N2 gas was still present and the internal pressure within the carburization room was 100 kPa. After this condition had been kept for 30 minutes, the internal pressure within the carburization room 17 was reduced to 0.1 kPa by virtue of gas discharge, while the steel material was transported to the quenching room 19 by way of the transportation room 16, thereby starting the oil quenching treatment.
The average carbon concentration distribution of the steel material treated in this example is shown in
In this way, since the treatment temperature was set at 1050° C., which is a high temperature, and since the carbon potential was set at 1.4%, the carburization lead time of the carburization treatment in Example 2 could be greatly reduced. In fact, the carburization lead time in this example was reduced by about 73% compared with the aforementioned conventional gas carburization treatment (which uses an endothermic gas). Accordingly, using the carburization treatment method actually carried out in Example 2, it becomes possible to obtain a carburized layer having a desired depth, using a reduced time period than that required by the above described conventional gas carburization treatment (which uses an endothermic gas). Therefore, it is possible to reduce the total energy consumption. Moreover, since there is no soot being generated, the pieces of steel material can be placed at any position within the furnace without any limitation. In this way, the use of the present invention makes it possible to obtain carburized layers which are relatively uniform and differ little from each other in their physical and chemical properties.
Example 3 was conducted based on Example 1 but using a different carburization pressure from that used in Example 1. Namely, sections of steel material pieces which were identical to those used in Example 1 were disposed at nine positions within the carburization room 17 whose internal temperature was controlled at 950° C. and whose internal pressure was controlled at 0.1 kPa or lower. Then, the pressure within the carburization room 17 was restored to 100 kPa by charging the room with N2 gas, while the internal temperature thereof was kept at 950° C.
After the carburization room 17 had been kept under the above described conditions for 30 minutes, its internal pressure was reduced to 0.1 kPa by virtue of gas discharge. Subsequently, C3H8 gas and CO2 gas were supplied into the carburization room 17, each at a flow rate of 15 L/min so as to increase the internal pressure to 100 kPa.
Next, with the internal pressure of the carburization room 17 kept at 100 kPa, the supply amount of CO2 gas and/or the supply amount of C3H8 gas were changed so as to have the carbon potential controlled at 1.25%. Then, the interior of the carburization room 17 was kept at 950° C. for 57 minutes.
Subsequently, the supply of C3H8 gas and CO2 gas was stopped and the internal pressure within the carburization room 17 was reduced to 0.1 kPa by virtue of gas discharge. Then, this internal pressure was kept for 37 minutes, while the internal temperature of the carburization room 17 was lowered to 870° C. during a subsequent time period of 30 minutes. Afterwards, the steel material was transported to the quenching room 19 by way of the transportation room 16, hence starting the oil quenching treatment.
As a result, an effective carburization depth (0.36% C) of the treated steel material in this example was found to be 0.72 mm, which was an appropriate value, and no soot was generated.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2001-169635 | Jun 2001 | JP | national |
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| 06172960 | Jun 1994 | JP |
| Number | Date | Country | |
|---|---|---|---|
| 20020179187 A1 | Dec 2002 | US |
