Method for preparing pressed scandia-doped dispenser cathodes using microwave sintering

This application claims the priority benefit of Chinese Patent Application No. 201610366220.5, filed on May 27, 2016, titled “Method for preparing pressed scandia-doped dispenser cathodes using microwave sintering,” which is hereby incorporated by reference in its entirety.

The present disclosure belongs to the area of insoluble rare-earth metal cathode materials and a tungsten matrix composite and more particularly to a method for preparing pressed scandia-doped dispenser cathodes using microwave sintering.

Recently, micro-focus X-Ray (micro-focus:<100 um×100 um) is developed quickly in medical treatment, health and aerospace areas. The research and development of X-Ray devices with small focus and high power arouses researchers' attention from different technical areas. The key technology of micro-focus X-Ray application is a source of micro-focus X-Ray: cathode of micro-area X-Ray tube. However, with the fast improvement of resolution and power of tube electron, the needs of small size and high power cathode become urgent, and the research and development of cathodes with high dimensional accuracy and high current emission is more and more important.

Scandia-doped dispenser cathode is the highest emission cathode. However, the preparation of this kind of cathode is complicated since secondary deformation is caused by molten salt, the sintering process can't be finished on one time. It has poor repeatability and is not satisfied with the desirable cathode requirement of micro-area X-Ray tubes. The formation of pressed Scandia-doped dispenser cathode can be finished on one time, but active materials distribute heterogeneous, resulting in poor structure homogeneity. Further, high emission performance can't be reached. In normal cathode sintering, the heating rate of the traditional sintering furnace is 5-10° C./min, and it takes 350-400 min to finish the whole process. Thus, under conventional methods, a lot of energy is wasted and, a long cooling time of sintering process leads to grain growth while repeatability is poor.

Microwave sintering is a new sintering technology with immediacy such that materials are heated as long as there has a microwave radiation. When microwave radiation is stopped, a heating process is stopped immediately. Thus, the fast heating can be realized, and energy transforming rate of the microwave is high, and heating rate can be reached in 40-50° C./min and easier to reach 1600° C. Since the heating and cooling process is fast, ultrafine grain materials are obtained. Under microwave sintering, grain growth is restrained, the microstructure of materials is improved significantly, the mechanical property of fine grain is excellent, and the contraction ratio of microwave sintering is reduced significantly compare with normal sintering. Further, the vertical shrinkage and horizontal shrinkage of this sample are only one third as much as normal sintering samples.

In conclusion, there is a need for finding an energy saving and one-time forming sintering method with fast heating and cooling rate to obtain a cathode with homogeneous structure and fine grain size. It is meaningful for improving the performance of micro-focus X-Ray and developing of terahertz vacuum electronic devices.

Current technologies can't satisfy the development of micro-focus X-Ray and have some drawbacks, such as complicated preparation technique, low dimensional accuracy and the sintering process caused energy waste. The present disclosure discloses a preparation method of pressed Scandia-doped dispenser cathode by microwave sintering, one-time forming of cathode sintering is realized, and sintering shrinkage and sintering time are reduced significantly. Embodiments of the present disclosure have good repeatability with homogeneous structure and have excellent emission performance at 950° C.

To realize the goals mentioned above, technique schema used in the present disclosure includes the following steps:

A: preparation of precursor powder: dissolving ammonium metatungstate hydrate, scandium nitrate, aluminum nitrate, barium nitrate and calcium nitrate in water under room temperature, respectively, mixing ammonium metatungstate hydrate and scandium nitrate solution, and adding nitrate solution mentioned above slowly with constant agitation. In these instances, the concentration of the mixed solution is 40-80 g/L, precursor powder is obtained by spray-drying, feeding rate is 200 ml/h-600 ml/l, blast rate is 0.4 m 3 /min-0.6 m 3 /min and inlet temperature is: 150° C., the outlet temperature is 90-96° C.

B: decomposition and reduction of precursor powder: precursor powder is decomposed in muffle furnace, C and N contains in precursor powder is removed under the conditions of 550° C., air atmosphere (or oxygen atmosphere) and maintain 3 hours, oxide powder contains scandium oxide, and tungsten oxide is obtained; proceeding reduction process of the oxide powder in tube furnace under hydrogen atmosphere, which includes two steps, first, maintaining the temperature at 450-550° C. maintain 2-3 h, then, raising the temperature to 800-850° C. and maintaining 2-3 h to obtain doped tungsten powder.

C: cathode pressing process and microwave sintering: using molds to press the decomposed powder under a certain pressure of 0.8-1.2 t/cm 2 , putting green bodies in auxiliary heating and insulation combining device, then putting them in microwave cavity, turning on the microwave source, raising the temperature to 800-850° C. with a constant rate, then raising the temperature to 1400-1500° C. with 10˜15° C./min, insulate 10-30 min, and cooling to room temperature.

In step A, the proportion of an amount of ammonium metatungstate hydrate and scandium nitrate based on the manufactured scandia-doped dispenser cathode material is: W (85%), Sc 2 O 3 (5%), BaO, CaO and Al 2 O 3 (10%), (molar ratio of Ba:Ca:Al=4:1:1).

The composition of reduced powder generated by step B is W, Sc 2 O 3 , BaO, CaO, and Al 2 O 3 .

The auxiliary heating material of auxiliary heating and insulation combining device is SiC; insulation material is Mullite Fiber.

To describe the technique embodiments in detail, the appended drawings used in embodiments is introduced below. Apparently, appended drawings below are only a part of drawings of the present disclosure, and as for normal technician in this area, they can obtain other drawings based on this kind of appended drawings without creative labor.

FIG. 1 is a flow chart of the preparation method of the present disclosure.

FIG. 2 is a schematic diagram of microwave sintering device.

FIG. 3 is XRD results of powders after reduction.

FIG. 4 shows SEM photo and EDAX energy spectrum analysis of the present disclosure.

FIG. 5 shows cathode real photo and SEM photo of the present disclosure (a: cathode real photo, b: SEM photo of cathode surface of embodiments 1, c: SEM photo of cathode surface of embodiments 2, d: SEM photo of cathode surface of embodiments 3).

FIG. 6 is a cathode thermal emission curve (Log U-Log I) of three embodiments of the present disclosure.

The present disclosure will be described in more detail.

Dissolving barium nitrate (20.34 g), calcium nitrate tetrahydrate (4.60 g), aluminum nitrate nonahydrate (14.61 g), nitrate hexahydrate scandium (36.84 g) and ammonium metatungstate (160.668 g) in deionized water respectively, stirring until they are fully dissolved. Then preparing “411” solution, which includes barium nitrate, calcium nitrate and aluminum nitrate. Mix nitrate scandium solution and ammonium metatungstate solution, adding “411” solution slowly with constantly agitation to realize intensive mixing. Precursor powder is obtained by spray-drying, feeding rate is 600 ml/l, blast rate is 0.4 m 3 /min-0.6 m 3 /min, the inlet temperature is 150° C., the outlet temperature is 90-96° C. The precursor powder is decomposed in muffle furnace, C and N contains in precursor powder is removed under the conditions of 550° C., air atmosphere (or oxygen atmosphere) and maintain 3 hours, oxide powder contains scandium oxide, and tungsten oxide is obtained; proceeding reduction process of the oxide powder in tube furnace under hydrogen atmosphere, which includes two steps, first, maintaining the temperature at 500° C. maintain 2-3 h, then, raising the temperature to 900° C. and maintain 2-3 h to obtain, doped tungsten powder. At last, using molds to press the decomposed powder under pressure of 1.2 t/cm 2 , putting green bodies in auxiliary heating and insulation combining device, then putting them in microwave cavity, turning on the microwave source, raising the temperature to 850° C. with a constant rate of 20° C./min, then raising the temperature to 1500° C. with a constant rate of 13° C./min, maintaining the temperature for 20 min, and cooling to room temperature.

Dissolving barium nitrate (6.78 g), calcium nitrate tetrahydrate (1.53 g), aluminum nitrate nonahydrate (4.78 g), nitrate hexahydrate scandium (12.28 g) and ammonium metatungstate (56.61 g) in deionized water respectively, stirring until they are fully dissolved. Then preparing “411” solution, which includes barium nitrate, calcium nitrate and aluminum nitrate. Mixing nitrate scandium solution and ammonium metatungstate solution, and adding “411” solution slowly with constantly agitation to realize intensive mixing. Precursor powder is obtained by spray-drying, feeding rate is 600 ml/l, blast rate is 0.4 m 3 /min-0.6 m 3 /min, the inlet temperature is: 150° C., the outlet temperature is 90-96° C. The precursor powder is decomposed in muffle furnace, C and N contains in precursor powder is removed under the conditions of 550° C., air atmosphere (or oxygen atmosphere) and maintaining 3 hours, oxide powder contains scandium oxide, and tungsten oxide is obtained; proceeding reduction process of the oxide powder in tube furnace under hydrogen atmosphere, includes two steps, first, maintaining the temperature at 500° C. with 2-3 h, then, raising the temperature to 900° C. and maintain 2-3 h to obtain doped tungsten powder. At last, using molds to press the decomposed powder under pressure of 1.2 t/cm 2 , putting green bodies in auxiliary heating and insulation combining device, then putting them in microwave cavity, turning on the microwave source, raising the temperature to 850° C. with a constant rate of 20° C./min, then raising the temperature to 1500° C. with a constant rate of 15° C./min, maintaining the temperature for 15 min, and cooling to room temperature.

Dissolving barium nitrate (20.34 g), calcium nitrate tetrahydrate (4.60 g), aluminum nitrate nonahydrate (14.61 g), nitrate hexahydrate scandium (36.84 g) and ammonium metatungstate (160.668 g) in deionized water respectively, stirring until they are fully dissolved. Then prepare “411” solution, which includes barium nitrate, calcium nitrate and aluminum nitrate. Mixing nitrate scandium solution and ammonium metatungstate solution, add “411” solution slowly with constantly agitation to realize intensive mixing. Precursor powder is obtained by spray-drying, feeding rate is 300 ml/l, blast rate is 0.4 m 3 /min-0.6 m 3 /min, the inlet temperature is: 150° C., the outlet temperature is 90-96° C. The precursor powder is decomposed in muffle furnace, C and N contains in precursor powder is removed under the conditions of 550° C., air atmosphere (or oxygen atmosphere) and maintain 3 hours, oxide powder contains scandium oxide, and tungsten oxide is obtained; proceeding reduction process of the oxide powder in tube furnace under hydrogen atmosphere, includes two steps, first, maintaining the temperature at 500° C. with 2 h, then, raising the temperature to 900° C. and maintain 2 h to obtain doped tungsten powder. At last, using molds to press the decomposed powder under pressure of 1.2 t/cm 2 , putting green bodies in auxiliary heating and insulation combining device, then putting them in microwave cavity, turn on the microwave source, raising the temperature to 800-850° C. with a constant rate of 20° C./min, then raising the temperature to 1550° C. with a constant rate of 15° C./min, maintaining the temperature for 30 min, and cooling to room temperature.

The embodiments mentioned above just are a further description of the present disclosure, but the present disclosure is more illustrative than that. Any modifications, similar substitutions, and improvements based on the present disclosure should be included in the protective range of the present disclosure.