阅读说明：本技术 一种复合结构氧化铝陶瓷管壳及其制备方法 (Alumina ceramic tube shell with composite structure and preparation method thereof ) 是由 李俣荃 李飞 江彬彬 江勇 于 2021-08-26 设计创作，主要内容包括：本发明提供了一种复合结构氧化铝陶瓷管壳：管壳主体是由高铝瓷或细晶瓷或其二者组合组成；需要金属化部位是由一层低铝瓷或粗晶瓷或其二者组合组成。本发明同时提供了该复合结构氧化铝陶瓷管壳制备方法：首先配制含有可交联单体的高铝细晶瓷浆料和低铝粗晶瓷浆料,先将高铝细晶瓷浆料浇入模具并预留浇注空间,再将低铝粗晶瓷浆料浇入,然后加热引发固化形成坯体,坯体再经干燥和烧结即得到一种复合结构氧化铝陶瓷管壳。与现有的氧化铝陶瓷管壳相比,该管壳同时兼具了优异的力学性能和良好的可金属化性能,并且制备方法具有工序少,成本低等优势。(The invention provides an alumina ceramic tube shell with a composite structure, which comprises the following components in part by weight: the main body of the pipe shell is made of high-alumina porcelain or fine-grain porcelain or the combination of the high-alumina porcelain and the fine-grain porcelain; the metallized part is composed of a layer of low-aluminum porcelain or coarse crystal porcelain or the combination of the two. The invention also provides a preparation method of the alumina ceramic tube shell with the composite structure, which comprises the following steps: firstly, preparing high-aluminum fine-grain ceramic slurry and low-aluminum coarse-grain ceramic slurry containing crosslinkable monomers, firstly, pouring the high-aluminum fine-grain ceramic slurry into a mould and reserving a pouring space, then pouring the low-aluminum coarse-grain ceramic slurry into the mould, then heating and initiating to cure to form a blank body, and drying and sintering the blank body to obtain the aluminum oxide ceramic tube shell with the composite structure. Compared with the existing alumina ceramic tube shell, the tube shell has excellent mechanical property and good metallizability, and the preparation method has the advantages of few procedures, low cost and the like.)

1. The alumina ceramic tube shell with the composite structure is characterized in that the tube shell is formed by compounding alumina ceramics with different alumina contents, different grain sizes or the combination of the alumina ceramics and the grain sizes; wherein, the main body of the pipe shell is composed of high aluminum or fine grain porcelain or the combination of the high aluminum and the fine grain porcelain; the metallized part is composed of a layer of low-aluminum or coarse crystal porcelain or the combination of the two.

2. The composite alumina ceramic cartridge of claim 1 wherein the cartridge body is made of high alumina or fine grain ceramic or a combination of both, i.e., alumina content greater than 96% and average grain size less than 5 μm.

3. The alumina ceramic cartridge of claim 1, wherein the low aluminum or coarse ceramic or a combination thereof has an alumina content of 94% or less and an average grain size of 10 μm or more.

4. The alumina ceramic cartridge of claim 1, wherein the low-alumina coarse grain ceramic portion has a thickness of 1mm or less, and a transition layer of naturally formed gradient change in composition, grain size, etc. is provided between the high-alumina fine grain ceramic and the low-alumina coarse grain ceramic.

5. A method of making a composite structural alumina ceramic envelope as claimed in any one of claims 1 to 4, wherein the method comprises the steps of:

step one, uniformly mixing a monomer, deionized water and a dispersing agent to obtain a solution; wherein the monomer is acrylamide or methacrylamide and N, N-methylene bisacrylamide according to the ratio of (10-30): 1, the dosage is 1.5-3 percent of the weight of the ceramic powder to be added; the dispersant is ammonium polyacrylate, polyacrylamide or modified product thereof, and the dosage is 0.3-1.0% of the weight of the ceramic powder; the dosage of the deionized water is determined by the content of organic matters (monomer plus dispersant) in the solution being (18-22)%;

dividing the solution into two parts, adding high-aluminum fine-grain ceramic powder into one part, and adding low-aluminum coarse-grain ceramic powder into the other part; the adding amount of the porcelain powder is based on ensuring that the viscosity of the slurry after ball milling is within (80-200) mPa & s;

step three, ball-milling the two parts of alumina solution until no agglomeration exists, and respectively obtaining high-aluminum fine crystal porcelain slurry and low-aluminum coarse crystal porcelain slurry;

step four, filtering the two slurry, removing bubbles in vacuum, adding an initiator and a catalyst, and uniformly stirring; the initiator is ammonium persulfate or 2,2' -azo [2- (2-imidazoline-2-yl) propane ] dihydrochloride and the like, and the addition amount is 0.02-0.12 percent of the weight of the slurry;

step five, slowly pouring the high-aluminum fine-grain ceramic slurry into the mold until the lower edge of the part of the product to be metallized is reached, and then slowly pouring the low-aluminum coarse-grain ceramic slurry;

placing the mold poured with the slurry into hot water at the temperature of 40-60 ℃ for initiating solidification to obtain a blank;

step eight, demolding the blank, and drying for 24 hours in a high-humidity low-temperature environment;

taking out the blank, and continuously naturally airing or drying at 50-100 ℃;

step ten, sintering the dried green body;

step eleven, polishing and grinding two ends of the sintered blank to obtain the aluminum oxide ceramic tube shell with the composite structure.

Technical Field

The invention relates to an alumina ceramic tube shell, in particular to an alumina ceramic tube shell with a composite structure and a preparation method thereof, belonging to the technical field of ceramic materials.

Background

The alumina ceramic has the characteristics of small dielectric loss, large specific volume resistance, high strength, small thermal expansion coefficient, low cost and the like, and is widely used for arc extinguish chamber shells in electric vacuum devices. Because the alumina ceramic cannot be directly welded with the metal electrode and the like, when the aluminum oxide ceramic is used, the end face of the aluminum oxide ceramic is often required to be metalized firstly, so that the aluminum oxide ceramic can be welded with the metal electrode to form a sealed container, and the vacuum environment in the sealed container or the filled arc-extinguishing medium can be kept from leaking. Among various alumina ceramic metallizing methods, the active molybdenum-manganese method is widely used because of mature process, high bonding strength and good air tightness. The high bonding strength of the active molybdenum-manganese method metallization comes from a composite transition layer formed between metal and ceramic, and the composite transition layer is formed by interdiffusion and permeation of active ingredients in metallization materials such as manganese oxide, molybdenum oxide, silicon oxide and the like and glass phase ingredients in the ceramic. Research shows that in order to form a composite transition layer with high bonding strength and good air tightness, on one hand, alumina ceramics is required to contain a certain amount of transferable glass phases, and on the other hand, alumina ceramics is required to have a certain grain size and porosity so as to ensure the mutual permeation of the glass phases. Studies by high-ridge bridges and the like have suggested that to achieve high quality metallization layers, the glass phase content of the alumina ceramic generally needs to be above 5%, and the average grain size should be (12-16) um or larger.

Although the metallizing performance of the tube shell can be improved by high glass phase content or large grain size, the mechanical property of the tube shell is reduced, and the overlarge grain size has the defects of poor air tightness, high sintering temperature and the like, so that the performance requirement of a large vacuum product cannot be met. For example, the ceramic tube shell for vacuum switch tube (SJ/T11246-2001) in the electronic industry standard requires that the bending strength of an alumina tube shell is more than or equal to 280MPa, and the bending strength of a large-sized high-voltage vacuum tube is often required to be more than 350 MPa. Research is carried out on adding a small amount of zirconia into alumina ceramics to improve the bending strength of the alumina ceramics through phase change toughening, but the addition of the zirconia reduces the electrical properties of the alumina ceramics, and the requirements on dispersion, particle size matching and the like of two kinds of powder are high, so that the process difficulty is increased, and the cost is increased. Therefore, a new solution to solve the above technical problems is urgently needed.

Disclosure of Invention

Aiming at the problems in the prior art, the invention provides the alumina vacuum ceramic tube shell with the composite structure and the preparation method thereof.

In order to achieve the purpose, the technical scheme of the invention is that the alumina ceramic tube shell with the composite structure is formed by compounding alumina ceramics with different alumina contents, different grain sizes or the combination of the alumina ceramics and the grain sizes; wherein, the tube shell main body is composed of high-strength high aluminum or fine grain porcelain or the combination of the high aluminum and the fine grain porcelain (the content of alumina is higher than 96%, the average grain size is less than 5 μm, the high aluminum fine grain porcelain for short); the part needing metallization is composed of a layer of low-aluminum or coarse-grain porcelain easy to metallize or a combination of the low-aluminum or coarse-grain porcelain (the content of aluminum oxide is less than or equal to 94 percent, the average grain size is more than or equal to 10 mu m, the low-aluminum coarse-grain porcelain for short) and the thickness of the low-aluminum coarse-grain porcelain part is less than or equal to 1mm, and a transition layer with naturally formed gradient changes of components, grain sizes and the like is arranged between the high-aluminum fine-grain porcelain and the low-aluminum coarse-grain porcelain.

A preparation method of an alumina ceramic tube shell with a composite structure comprises the following steps:

step one, uniformly mixing a monomer, deionized water and a dispersing agent to obtain a solution; wherein the monomer is acrylamide or methacrylamide and N, N-methylene bisacrylamide according to the ratio of (10-30): 1, the dosage is 1.5-3 percent of the weight of the ceramic powder to be added; the dispersant is ammonium polyacrylate, polyacrylamide or modified product thereof, and the dosage is 0.3-1.0% of the weight of the ceramic powder; the dosage of the deionized water is determined by the content of organic matters (monomer plus dispersant) in the solution being (18-22)%;

dividing the solution into two parts, adding high-aluminum fine-grain ceramic powder into one part, and adding low-aluminum coarse-grain ceramic powder into the other part; the adding amount of the porcelain powder is based on ensuring that the viscosity of the slurry after ball milling is within (80-200) mPa & s;

step three, ball-milling the two parts of alumina solution until no agglomeration exists, and respectively obtaining high-aluminum fine crystal porcelain slurry and low-aluminum coarse crystal porcelain slurry;

step four, filtering the two slurry, removing bubbles in vacuum, adding an initiator and a catalyst, and uniformly stirring; the initiator is ammonium persulfate or 2,2' -azo [2- (2-imidazoline-2-yl) propane ] dihydrochloride and the like, and the addition amount is 0.02-0.12 percent of the weight of the slurry;

step five, slowly pouring the high-aluminum fine-grain ceramic slurry into the mold until the lower edge of the part of the product to be metallized is reached, and then slowly pouring the low-aluminum coarse-grain ceramic slurry;

placing the mold poured with the slurry into hot water at the temperature of 40-60 ℃ for initiating solidification to obtain a blank;

step eight, demolding the blank, and drying for 24 hours in a high-humidity low-temperature environment;

taking out the blank, and continuously naturally airing or drying at 50-100 ℃;

step ten, sintering the dried green body;

step eleven, polishing and grinding two ends of the sintered blank to obtain the aluminum oxide ceramic tube shell with the composite structure.

Compared with the prior art, the invention has the following advantages that 1) aiming at the existing large-scale non-composite structure alumina ceramic tube shell, the invention has the contradiction that the mechanical strength and the easy metallization characteristic are difficult to meet simultaneously, the invention provides the composite structure: the main body of the tube shell adopts high-alumina fine-grain porcelain, so that the characteristic that the strength of the alumina porcelain is improved along with the reduction of the grain size or the reduction of the content of the glass phase is fully utilized, and the high main body strength is obtained. The low-aluminum coarse-crystal ceramic thin layer is adopted at the position needing metallization, so that the metallizing capability is improved, and the comprehensive performance of the product is effectively improved; 2) in the aspect of the reliability of the composite structure, on one hand, the thickness of the low-aluminum coarse-grain ceramic part is small, and on the other hand, the wet forming is adopted, so that a transition layer with gradient change of composition or grain size and the like is naturally formed between the high-aluminum fine-grain ceramic and the low-aluminum coarse-grain ceramic by utilizing the characteristic that slurry can be mutually diffused, and therefore, the defects of the connection parts of the high-aluminum fine-grain ceramic and the low-aluminum coarse-grain ceramic due to the difference of physical and chemical characteristics of the ceramic bodies can be avoided, and high-reliability connection is formed. In addition, compared with the existing isostatic pressing production process, the isostatic pressing production process cannot directly prepare the tube shell with a composite structure, in addition, the equipment cost is only 1/10 of the isostatic pressing process, the die cost is 1/2 of the isostatic pressing process, the procedures of blank processing and the like are saved, and the comprehensive cost is lower than that of the isostatic pressing process by more than 30 percent.

Drawings

FIG. 1 is a schematic structural diagram of a circular alumina ceramic tube with a composite structure.

In the figure: 1. 94 alumina, 2 composite transition layer, 3, 96 alumina.

The specific implementation mode is as follows:

for the purpose of enhancing an understanding of the present invention, the present embodiment will be described in detail below with reference to the accompanying drawings.

Example 1: referring to fig. 1, the alumina ceramic envelope with a circular composite structure shown in fig. 1 has a main body composed of 96 alumina 3 and an average grain size of 5 μm, and a portion to be metallized is composed of a layer of 94 alumina 1 and has an average grain size of 10 μm and a thickness of 0.5 mm; the preparation method of the ceramic tube shell with the composite structure comprises the following steps:

step one, uniformly mixing 19g of acrylamide, 1g of N, N-methylene bisacrylamide, 106g of deionized water and 10g of ammonium polyacrylate to obtain a solution with the organic matter content of 22%;

step two, weighing 108g of solution, and adding 800g of 96 alumina porcelain powder with the average grain diameter of 1 mu m; weighing 28g of solution, and adding 200g of 94 alumina porcelain powder with the average grain diameter of 3 mu m;

step three, respectively carrying out ball milling on the two slurry parts until no agglomeration exists, and measuring the viscosities of the slurry parts to be 162 mPa & s and 95mPa & s respectively;

step four, filtering the two slurry, removing bubbles in vacuum, adding 10g and 0.5g of 10% ammonium persulfate solution, and uniformly stirring;

step five, slowly pouring the high-alumina ceramic slurry into the mold until the lower edge of the part of the product needing metallization is higher, and then slowly pouring the low-alumina ceramic slurry;

sixthly, placing the mold poured with the slurry into hot water at the temperature of 40 ℃ for initiating for 1.5 hours to obtain a solidified blank;

step eight, demolding the blank, and drying for 24 hours in an environment with the relative humidity of 92%;

step nine, taking out the blank body, and continuing to naturally dry the blank body;

step ten, sintering the dried blank at 1620 ℃, preserving heat for 2 hours, and naturally cooling to obtain the alumina ceramic tube shell with the composite structure.

The bending strength of the prepared 96 porcelain of the composite tube shell main body is 345MPa, the metalized sealing strength is 160MPa, the bending strength is superior to 280MPa and 80MPa required in the ceramic tube shell for vacuum switch tubes in the electronic industry standard, and the special requirement that the bending strength of the product is more than 350MPa is met.

Example 2:

a circular alumina ceramic tube shell with a composite structure comprises a main body made of 99 alumina, wherein the average grain size is 2 mu m, a part needing metallization is made of a layer of 92 alumina, the average grain size is 4 mu m, and the thickness of the 92 alumina layer is 0.5 mm; between 99 and 92 aluminas, there is a naturally occurring transition layer.

The preparation method of the ceramic tube shell with the composite structure comprises the following steps:

uniformly mixing 29g of acrylamide, 1g of N, N-methylene bisacrylamide, 130g of deionized water and 3g of ammonium polyacrylate to obtain a solution with the organic matter content of 20%;

step two, weighing 133g of solution, and adding 800g of 99 alumina porcelain powder with the average grain diameter of 0.8 mu m; weighing 30g of the solution, and adding 200g of 92 alumina porcelain powder with the average grain diameter of 1 mu m;

step three, respectively carrying out ball milling on the two slurry parts until no agglomeration exists, and measuring the viscosities of the slurry parts to be 143 and 87mPa & s respectively;

step four, filtering the two slurry, removing bubbles in vacuum, adding 4g and 2.5g of 2,2' -azo [2- (2-imidazoline-2-yl) propane ] dihydrochloride solution with the concentration of 10%, and uniformly stirring;

step five, slowly pouring the high-alumina ceramic slurry into the mold until the lower edge of the part of the product needing metallization is higher, and then slowly pouring the low-alumina ceramic slurry;

sixthly, placing the mold poured with the slurry into hot water at 60 ℃ for initiating for 0.5h to obtain a solidified blank;

step eight, demolding the blank, and drying for 24 hours in an environment with the relative humidity of 90%;

step nine, taking out the blank body, and continuing to naturally dry the blank body;

and step ten, sintering the dried blank at 1600 ℃, preserving heat for 2 hours, naturally cooling, and grinding two ends to be flat to obtain the alumina ceramic tube shell with the composite structure.

The bending strength of the prepared composite tube shell main body 99 ceramic is 410MPa, the metalized sealing strength is 140MPa, the composite tube shell main body is superior to 280MPa and 80MPa required in the ceramic tube shell for vacuum switch tubes in the electronic industry standard, and the special requirement that the bending strength of a product is more than 350MPa is met.

Example 3:

a circular alumina ceramic tube shell with a composite structure is characterized in that a main body of the tube shell is made of 98 alumina, the average grain size is 2 mu m, a part needing metallization is made of a layer of 93 alumina, the average grain size is 6 mu m, and the thickness of the 93 alumina layer is 0.8 mm; between the 98 and 93 aluminas, there is a naturally occurring transition layer.

The preparation method of the ceramic tube shell with the composite structure comprises the following steps:

step one, uniformly mixing 14g of acrylamide, 1g of N, N-methylene bisacrylamide, 95g of deionized water and 6g of ammonium polyacrylate to obtain a solution with the organic matter content of 18%;

step two, weighing 94g of solution, and adding 800g of 98-alumina porcelain powder with the average grain diameter of 0.8 mu m; weighing 22g of solution, and adding 200g of 93-alumina porcelain powder with the average grain diameter of 4 mu m;

step three, ball-milling the two parts of slurry until no agglomeration exists, and measuring the viscosities of the slurry to be 191 and 137mPa & s respectively;

step four, filtering the two slurry, removing bubbles in vacuum, adding 10g and 2g of 2,2' -azo [2- (2-imidazoline-2-yl) propane ] dihydrochloride solution with the concentration of 10%, and uniformly stirring;

step five, slowly pouring the high-alumina ceramic slurry into the mold until the lower edge of the part of the product needing metallization is higher, and then slowly pouring the low-alumina ceramic slurry;

sixthly, placing the mold poured with the slurry into hot water at the temperature of 50 ℃ for initiating for 1h to obtain a solidified blank;

step eight, demolding the blank, and drying for 24 hours in an environment with the relative humidity of 95%;

step nine, taking out the blank body, and continuing to naturally dry the blank body;

and step ten, sintering the dried blank at 1610 ℃, preserving heat for 2 hours, naturally cooling, and grinding two ends to be flat to obtain the alumina ceramic tube shell with the composite structure.

The bending strength of the 98 porcelain of the prepared composite tube shell main body is 382MPa, the metalized sealing strength is 143MPa, the ceramic tube shell is superior to 280MPa and 80MPa required in the ceramic tube shell for vacuum switch tubes in the electronic industry standard, and the special requirement that the bending strength of the product is more than 350MPa is met.

It should be noted that the above-mentioned embodiments are not intended to limit the scope of the present invention, and all equivalent modifications and substitutions based on the above-mentioned technical solutions are within the scope of the present invention as defined in the claims.