Patent Grant
9646796
This application claims priority benefit of Chinese application No. 201310723707.0 filed on Dec. 24, 2013, the content of which is herein incorporated by reference in its entirety.
The present disclosure relates to a carburized lutetium oxide (Lu2O3) doped molybdenum (Mo) cathode and its fabrication method, which belongs to the technical field of rare earth-refractory metal cathodes.
Electron tubes and magnetrons have been used extensively in radar, navigation, electronic countermeasure, and microwave devices. Thermionic emission cathode is one of the key components of electron tubes and magnetrons and plays an important role in the operation of these devices. Up to now, thoriated cathode (ThO2—W) which is still widely used in electron tube and microwave oven magnetrons. Nevertheless, it is necessary to find other environment-friendly elements to substitute thorium as thorium is a radioactive element. Lanthanum oxide-molybdenum (La2O3—Mo) cathode was found to have a certain thermionic emission property. However, during the operation of magnetrons at an external magnetic field, a large number of electrons emitted back-bombarded the La2O3—Mo cathode, resulting in the evaporation and loss of lanthanum on the cathode surface and thus the poor emission stability of this kind of cathode. Among all the rare earth elements, lutetium (Lu) has the highest melting point. In this patent, we propose a kind of Lu2O3 doped Mo cathode for thermionic emission and its fabrication methods.
The present disclosure provides a carburized lutetium oxide doped molybdenum cathode and its fabrication method. The Lu2O3 doped Mo powder is prepared by sol-gel method in which solutions of lutetium nitrate (Lu(NO3)3), ammonium molybdate ((NH4)6Mo7O24), and citric acid (C6H8O7) are employed. The prepared powder is die-pressed to form pellets before they are sintered and carburized to obtain carburized Lu2O3 doped Mo cathodes.
In some embodiments, the quantity of lutetium oxide ranges from 1 to 4% by weight.
In some embodiments, the mass of citric acid is 1 to 1.3 times of (NH4)6Mo7O24.4H2O.
In some embodiments, the Lu2O3 doped Mo powder is prepared by Sol-Gel method, with addition of Lu(NO3)3 solution and citric acid into (NH4)6Mo7O24 solution simultaneously and slowly.
In some embodiments, the wet gel is calcined in air atmosphere at a temperature between 500 and 600° C. until the wet gel is calcined completely.
In some embodiments, the Lu2O3 doped Mo powder is obtained from the xerogel by two steps: firstly, the xerogel is calcined in hydrogen atmosphere at 500-550° C. for 2 h to obtain the Lu2O3 doped MoO2 powder, secondly, the powder from the first step is further calcined in hydrogen at 850-950° C. for 2 h to obtain the Lu2O3 doped Mo powder.
In some embodiments, the pellet is sintered in hydrogen at 1800-2000° C. for 60-120 min to obtain a cathode.
In some embodiment, the cathode is carburized in activated carbon powder at 1400-1500° C. for 5-20 min.
There are a number of advantages provided by the techniques employed in the present disclosure. The sol-gel method exhibits excellent mixture of Lu2O3 and Mo powders. The rare earth oxide in the substrate exhibits favorable thermionic emission performances, i.e. the maximum thermionic emission current density for the cathode containing 4 wt % Lu2O3 is 1.02 A/cm2 at 1400° C., similar to that of the Mo cathode containing 4 wt % La2O3. Furthermore, the Mo cathode with 3 wt % Lu2O3 meets the requirement of thermionic emission current densities of 0.3-0.8 A/cm2 for microwave oven magnetrons.
The techniques of the present disclosure are described in detail with reference to the accompanying drawings.
In the following description, the carburized Lu2O3 doped Mo cathode is obtained according to the present disclosure.
In some embodiments, the concentration of the rare earth oxide ranges from 1-4 wt %.
In some embodiments, the mass of citric acid is 1-1.3 times of ammonium heptamolybdate.
In some embodiments, the order of mixing the solution is to add the Lu(NO3)3 solution and the citric acid solution into the (NH4)6Mo7O24 solution simultaneously and slowly.
In some embodiments, the wet-gel is calcined at 500-600° C. in an electric furnace until the wet gel is calcined completely.
In some embodiments, the Lu2O3 doped molybdenum powder is developed in two steps: firstly, the xerogel is calcined at 500-550° C. for 2 h in hydrogen atmosphere to obtain the Lu2O3 doped MoO2 powder; secondly, the powder from the first step is further calcined at 850-950° C. for 2 h in hydrogen to obtain the Lu2O3 doped Mo powder.
In some embodiments, the pellets are sintered at 1800-2000° C. for 60-120 min in hydrogen to obtain cathodes.
In some embodiment, the cathode is carburized in activated carbon powder at 1400-1500° C. for 5-20 min.
The emission performance of the carburized Lu2O3 doped Mo cathode manufactured according to the present disclosure is evaluated at different activation temperatures (
Aqueous solutions of Lu(NO3)3, (NH4)6Mo7O24 and citric acid were made by dissolving 0.419 g Lu(NO3)3.H2O, 19.838 g (NH4)6Mo7O24.4H2O, 20.257 g of C6H8O7.H2O in de-ionized water, respectively. Afterwards, the solutions of Lu(NO3)3 and citric acid were added into the (NH4)6Mo7O24 solution simultaneously and slowly. A wet gel was formed after a couple of hours. The wet gel was transferred to a container and was baked to a xerogel in a drying oven. The xerogel is calcined in an electric furnace at 500° C., followed by calcining in dry hydrogen at 500° C. for 2 h and then 850° C. for 2 h to obtain Lu2O3 doped molybdenum powder. The powder is carefully grinded and sieved through a standard screen of 200-mesh. 0.081 g of the powder was measured and pressed into pellets of size Φ3×2 mm. The pellets were sintered at 1800° C. for 60 min in hydrogen, followed by carburization in activated carbon powder at 1400° C. for 20 min to obtain carburized Lu2O3 doped molybdenum cathodes. The thermionic emission current density of the cathode was tested at 1400° C. after being activated at 1600° C.
Aqueous solutions of Lu(NO3)3, (NH4)6Mo7O24 and citric acid were made by dissolving 0.533 g Lu(NO3)3.H2O, 25.248 g (NH4)6Mo7O24.4H2O, 25.781 g C6H8O7.H2O in de-ionized water, respectively. Afterwards, the solutions of Lu(NO3)3 and citric acid were added into the (NH4)6Mo7O24 solution simultaneously and slowly. A wet gel was formed after a couple of hours. The wet gel was transferred to a container and was baked into a xerogel in a drying oven. The xerogel is calcined in an electric furnace at 500° C., followed by calcining in dry hydrogen at 500° C. for 2 h and then a higher temperature of 800° C. for 2 h to obtain Lu2O3 doped molybdenum powder. The powder is carefully grinded and sieved through a standard screen of 200-mesh. 0.081 g of the powder was measured and pressed into pellets of size Φ3×2 mm. The pellets were sintered at 1900° C. for 60 min in hydrogen, followed by carburization in activated carbon powder at 1400° C. for 20 min to obtain carburized Lu2O3 doped molybdenum cathodes. The thermionic emission current density of the cathode was tested at 1400° C. after being activated at 1600° C.
Aqueous solutions of Lu(NO3)3, (NH4)6Mo7O24 and citric acid were made by dissolving 0.191 g Lu(NO3)3.H2O, 18.218 g (NH4)6Mo7O24.4H2O, 1.000 g C6H8O7.H2O in de-ionized water, respectively. Afterwards, the solutions of Lu(NO3)3 and citric acid were added into the (NH4)6Mo7O24 solution simultaneously and slowly. A wet gel was formed after a couple of hours. The wet gel was transferred to a container and was baked in a drying oven to develop a xerogel. The xerogel is calcined in an electric furnace at 600° C., followed by calcining in dry hydrogen at 500° C. for 2 h and then a higher temperature of 850° C. for 2 h to obtain Lu2O3 doped molybdenum powder. The powder is carefully grinded and sieved through a standard screen of 200-mesh. 0.081 g of the powder was measured and pressed into pellets of size Φ3×2 mm. The pellets were sintered at 2000° C. for 60 min in hydrogen, followed by carburization in activated carbon powder at 1400° C. for 20 min to obtain carburized Lu2O3 doped molybdenum cathodes. The thermionic emission current density of the cathode was tested at 1400° C. after being activated at 1600° C.
Aqueous solutions of Lu(NO3)3, (NH4)6Mo7O24 and citric acid were made by dissolving 0.743 g Lu(NO3)3.H2O, 23.205 g (NH4)6Mo7O24.4H2O, 23.948 g C6H8O7.H2O in de-ionized water, respectively. Afterwards, the solutions of Lu(NO3)3 and citric acid were added into the (NH4)6Mo7O24 solution simultaneously and slowly. A wet gel was formed after a couple of hours. The wet gel was transferred to a iron container and was baked in a drying oven to develop a xerogel. The xerogel is calcined in an electric furnace at 600° C., followed by calcining in dry hydrogen at 550° C. for 2 h and then a higher temperature of 900° C. for 2 h to obtain Lu2O3 doped molybdenum powder. The powder is carefully grinded and sieved through a standard screen of 200-mesh. 0.081 g of the powder was measured and pressed into pellets of size Φ3×2 mm. The pellets were sintered at 2000° C. for 60 min in hydrogen, followed by carburization in activated carbon powder at 1400° C. for 20 min to obtain carburized Lu2O3 doped molybdenum cathodes. The thermionic emission current density of the cathode was tested at 1400° C. after being activated at 1600° C.
Aqueous solutions of Lu(NO3)3, (NH4)6Mo7O24 and citric acid were made by dissolving 0.800 g Lu(NO3)3.H2O, 24.990 g (NH4)6Mo7O24.4H2O, 25.790 g C6H8O7.H2O in de-ionized water, respectively. Afterwards, the solutions of Lu(NO3)3 and citric acid were added into the (NH4)6Mo7O24 solution simultaneously and slowly. A wet gel was formed after a couple of hours. The wet gel was transferred to a container and was baked in a drying oven to develop a xerogel. The xerogel is calcined in an electric furnace at 550° C., followed by calcining in dry hydrogen at 550° C. for 2 h and then a higher temperature of 900° C. for 2 h to obtain Lu2O3 doped molybdenum powder. The powder is carefully grinded and sieved through a standard screen of 200-mesh. 0.081 g of the powder was measured and pressed into pellets of size Φ3×2 mm. The pellets were sintered at 1900° C. for 120 min in hydrogen, followed by carburization in activated carbon powder at 1400° C. for 20 min to obtain carburized Lu2O3 doped molybdenum cathodes. The thermionic emission current density of the cathode was tested at 1400° C. after being activated at 1600° C.
Aqueous solutions of Lu(NO3)3, (NH4)6Mo7O24 and citric acid were made by dissolving 0.629 g Lu(NO3)3.H2O, 19.635 g (NH4)6Mo7O24.4H2O, 20.246 g C6H8O7.H2O in de-ionized water, respectively. Afterwards, the solutions of Lu(NO3)3 and citric acid were added into the (NH4)6Mo7O24 solution simultaneously and slowly. A wet gel was formed after a couple of hours. The wet gel was transferred to a container and was baked in a drying oven to develop a xerogel. The xerogel is calcined in an electric furnace at 550° C., followed by calcining in dry hydrogen at 550° C. for 2 h and then a higher temperature of 900° C. for 2 h to obtain Lu2O3 doped molybdenum powder. The powder is carefully grinded and sieved through a standard screen of 200-mesh. 0.081 g of the powder was measured and pressed into pellets of size Φ3×2 mm. The pellets were sintered at 1900° C. for 60 min in hydrogen, followed by carburization in activated carbon powder at 1400° C. for 20 min to obtain carburized Lu2O3 doped molybdenum cathodes. The thermionic emission current density of the cathode was tested at 1400° C. after being activated at 1600° C.
Aqueous solutions of Lu(NO3)3, (NH4)6Mo7O24 and citric acid were made by dissolving 0.971 g Lu(NO3)3.H2O, 30.345 g (NH4)6Mo7O24H2O, 31.316 g C6H8O7.H2O in de-ionized water, respectively. Afterwards, the solutions of Lu(NO3)3 and citric acid were added into the (NH4)6Mo7O24 solution simultaneously and slowly. A wet gel was formed after a couple of hours. The wet gel was transferred to a container and was baked in a drying oven to develop a xerogel. The xerogel is calcined in an electric furnace at 550° C., followed by calcining in dry hydrogen at 550° C. for 2 h and then a higher temperature of 900° C. for 2 h to obtain Lu2O3 doped molybdenum powder. The powder is carefully grinded and sieved through a standard screen of 200-mesh. 0.081 g of the powder was measured and pressed into pellets of size Φ3×2 mm. The pellets were sintered at 1900° C. for 60 min in hydrogen, followed by carburization in activated carbon powder at 1500° C. for 10 min to obtain carburized Lu2O3 doped molybdenum cathodes. The thermionic emission current density of the cathode was tested at 1400° C. after being activated at 1600° C.
Aqueous solutions of Lu(NO3)3, (NH4)6Mo7O24 and citric acid were made by dissolving 1.067 g Lu(NO3)3.H2O, 24.733 g (NH4)6Mo7.4H2O, 25.800 g C6H8O7H2O in de-ionized water, respectively. Afterwards, the solutions of Lu(NO3)3 and citric acid were added into the (NH4)6Mo7O24 solution simultaneously and slowly. A wet gel was formed after a couple of hours. The wet gel was transferred to a container and was baked in a drying oven to develop a xerogel. The xerogel is calcined in an electric furnace at 550° C., followed by calcining in dry hydrogen at 550° C. for 2 h and then a higher temperature of 900° C. for 2 h to obtain Lu2O3 doped molybdenum powder. The powder is carefully grinded and sieved through a standard screen of 200-mesh. 0.081 g of the powder was measured and pressed into pellets of size Φ3×2 mm. The pellets were sintered at 1900° C. for 60 min in hydrogen, followed by carburization in activated carbon powder at 1500° C. for 10 min to obtain carburized Lu2O3 doped molybdenum cathodes. The thermionic emission current density of the cathode was tested at 1400° C. after being activated at 1600° C.
The maximum thermionic emission current densities of the cathodes fabricated from Example 1 to 8 are summarized in Table 1.
From the foregoing, it will be appreciated that, although specific embodiments of the present disclosure have been described herein for purposes of illustration, various modifications may be made without deviating from the spirit and scope of the present disclosure. Accordingly, the present disclosure is not limited except as by the appended claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2013 1 0723707 | Dec 2013 | CN | national |
