阅读说明：本技术 陶瓷材料的烧结控制方法 (Sintering control method of ceramic material ) 是由 林宗立 林致扬 陈龙怡 陈家洁 于 2019-06-03 设计创作，主要内容包括：本发明提供一种陶瓷材料的烧结控制方法。此方法包含有下列步骤：S1:制备含有一致孔材料的一致孔剂；S2:混合致孔剂与一陶瓷材料并形成一生坯；S3:于一无氧环境中以一第一温度烧结生坯以形成一陶瓷粗胚；以及S4:于一含氧环境中以一第二温度烧结陶瓷粗胚以形成一陶瓷物件。其中,第一温度高于第二温度。当致孔材料为一碳基材料,第二温度介于300℃至600℃,且孔隙率可达到30％至70％。藉此方法,陶瓷物件的硬度与致密度被提高,且得以准确调控陶瓷物件的孔隙率以及孔洞的形状和尺寸。(The invention provides a sintering control method of a ceramic material. The method comprises the following steps: s1, preparing a uniform pore agent containing a uniform pore material; s2, mixing the pore-foaming agent and a ceramic material to form a green body; s3, sintering the green compact in an oxygen-free environment at a first temperature to form a ceramic blank; and S4, sintering the ceramic blank in an oxygen-containing environment at a second temperature to form a ceramic object. Wherein the first temperature is higher than the second temperature. When the pore-forming material is a carbon-based material, the second temperature is between 300 ℃ and 600 ℃, and the porosity can reach 30% to 70%. By the method, the hardness and the density of the ceramic object are improved, and the porosity of the ceramic object and the shape and the size of the hole can be accurately regulated and controlled.)

1. A sintering control method of ceramic material is characterized by comprising the following steps:

s1, preparing a uniform pore agent containing a uniform pore material;

s2, mixing the pore-forming agent and a ceramic slurry to form a green body;

s3, sintering the green body in an oxygen-free environment at a first temperature to form a ceramic blank; and

s4, sintering the ceramic blank in an oxygen-containing environment at a second temperature to form a ceramic object;

wherein the second temperature is lower than the first temperature.

2. The method of claim 1, wherein in step S1, the pore-forming material is a carbon-based material, an ore, a salt, a natural fiber, or a polymer, and the carbon-based material is carbon fiber, carbon nanotube, graphene, or expanded graphite.

3. The sintering control method of ceramic material according to claim 2, wherein in step S1, the carbon-based material has a shape of sphere, plate, irregular, strip, or cube.

4. The method of claim 1, wherein in step S1, the pore-forming material has a size of 50nm to 400 μm.

5. The method for controlling sintering of a ceramic material according to claim 1, wherein step S2 further comprises the following substeps:

s21, mixing the pore-forming agent and the ceramic slurry according to a predetermined ratio to form a mixed raw material; and

s22, printing the mixed raw material by using lamination manufacturing technique to form the green body.

6. The method of claim 5, wherein in step S21, the porogen accounts for 10-50% of the predetermined ratio of the mixed raw materials.

7. The method for controlling sintering of a ceramic material according to claim 1, wherein step S3 further comprises the following substeps:

s31, introducing a stable gas into a predetermined environment to form the oxygen-free environment; and

s32, sintering the green body in the oxygen-free environment at a first temperature to form the ceramic rough blank.

8. The method of claim 7, wherein in step S31, the stable gas is nitrogen, and in step S32, the first temperature is higher than 600 ℃.

9. The method for controlling sintering of a ceramic material according to claim 1, wherein step S4 further comprises the following substeps:

s41, introducing air into a predetermined environment to form the oxygen-containing environment; and

s42, sintering the ceramic blank in the oxygen-containing environment for 1 to 10 hours at the second temperature to form the ceramic object, wherein the second temperature is between 300 ℃ and 600 ℃.

10. The sintering control method of ceramic material as claimed in claim 1, wherein in step S4, the porosity of the ceramic article is 30% to 70%.

Technical Field

The invention provides a sintering control method of a ceramic material, in particular to a method for controlling the porosity and the pore size of the ceramic material by multi-stage sintering.

Background

Ceramic engineering is a scientific technique for manufacturing objects using inorganic non-metallic materials. In recent years, ceramic materials have been widely used in material engineering, electronic engineering, chemical engineering, and mechanical engineering. Since ceramics are generally very heat resistant, they can be used in many applications where metals and high molecular weight polymers are not sufficient, such as mining, aerospace, biomedical, refining, food and chemical plants, electronics, industrial electrical transmission, and optical waveguide transmission, among others.

In accordance with different industries, the specifications and characteristics of ceramics have different requirements. In the biomedical field, in order to develop a replacement implant for human bone, it is necessary to grasp the porosity of the implant. Porosity has a significant impact on the physical and chemical interactions between the implant and the surrounding tissue. Porosity increases the available surface area for cell interaction, for example: affecting the mechanical integration of the implant at the implantation site, and the rate of implant resorption. Preferably, the porosity of the implant is replication of natural tissue. For example: in segmental (segmented) bone defects, a highly porous central portion (mimicking trabecular bone) is surrounded by a stronger and less porous shell (mimicking cortical bone) to provide structural support.

However, during the sintering of ceramics, the porosity becomes a factor difficult to control accurately due to the change of molecular arrangement caused by temperature, which affects the uncertainty of the quality of the sintered product. To accurately adjust the porosity, low temperature processes are commonly used in the industry, which sacrifice the mechanical strength of the ceramic material. Therefore, there is a need for a new ceramic sintering technique that can accurately control the porosity and pore size and can sinter high-strength and high-density ceramics at a sufficiently high temperature.

Disclosure of Invention

In view of the above, the present invention provides a sintering control method for a ceramic material, which can overcome the defects of the prior art, improve the compactness and the mechanical strength, and avoid the porosity loss after high temperature sintering.

In order to achieve the purpose, the invention discloses a sintering control method of a ceramic material, which is characterized by comprising the following steps:

s1, preparing a uniform pore agent containing a uniform pore material;

s2, mixing the pore-forming agent and a ceramic slurry to form a green body;

s3, sintering the green body in an oxygen-free environment at a first temperature to form a ceramic blank; and

s4, sintering the ceramic blank in an oxygen-containing environment at a second temperature to form a ceramic object;

wherein the second temperature is lower than the first temperature.

In step S1, the pore-forming material is a carbon-based material, an ore, a salt, a natural fiber, or a polymer, and the carbon-based material is carbon fiber, carbon nanotube, graphene, or expanded graphite.

In step S1, the carbon-based material is spherical, plate-shaped, irregular, strip-shaped, or cubic.

In step S1, the pore-forming material has a size of 50nm to 400 μm.

In step S2, the method further includes the following sub-steps:

s21, mixing the pore-forming agent and the ceramic slurry according to a predetermined ratio to form a mixed raw material; and

s22, printing the mixed raw material by using lamination manufacturing technique to form the green body.

In step S21, the porogen accounts for 10% to 50% of the predetermined ratio of the mixed raw material.

In step S3, the method further includes the following sub-steps:

s31, introducing a stable gas into a predetermined environment to form the oxygen-free environment; and

s32, sintering the green body in the oxygen-free environment at a first temperature to form the ceramic rough blank.

Wherein, in step S31, the stable gas is nitrogen, and in step S32, the first temperature is higher than 600 ℃.

In step S4, the method further includes the following sub-steps:

s41, introducing air into a predetermined environment to form the oxygen-containing environment; and

s42, sintering the ceramic blank in the oxygen-containing environment for 1 to 10 hours at the second temperature to form the ceramic object, wherein the second temperature is between 300 ℃ and 600 ℃.

In step S4, the porosity of the ceramic article is 30% to 70%.

In summary, the sintering control method of the ceramic material of the present invention is to mix the pore-forming material as the pore-forming agent with the ceramic material. Then, by using two stages of sintering, oxygen-free air and oxygen-containing air are respectively introduced, and the corresponding sintering temperatures are controlled. Therefore, the obtained ceramic object has the advantages of compactness and mechanical strength after high-temperature sintering, and porosity loss after high-temperature sintering is avoided. Particularly, by adjusting the proportion, shape and size of the carbon-based material, the porosity and the shape of the holes in the ceramic object can be accurately regulated and controlled, so that the ceramic object can be accurately simulated and applied to various industrial requirements.

Drawings

FIG. 1: a flow chart of a sintering control method for a ceramic material according to an embodiment of the invention is shown.

FIG. 2: a flow chart of a sintering control method for a ceramic material according to another embodiment of the present invention is shown.

FIG. 3: a flow chart of a sintering control method for a ceramic material according to another embodiment of the present invention is shown.

FIG. 4: a flow chart of a sintering control method for a ceramic material according to another embodiment of the present invention is shown.

FIG. 5: the effect of the ratio of carbon-based material on porosity in one embodiment of the present invention is illustrated.

Detailed Description

In order that the advantages, spirit and features of the invention will be readily understood and appreciated, embodiments thereof will be described and illustrated with reference to the accompanying drawings. It is to be understood that these embodiments are merely representative examples of the present invention, and that no limitations are intended to the scope of the invention or its corresponding embodiments, particularly in terms of the specific methods, devices, conditions, materials, and so forth.

In the description of the present invention, it is to be understood that the terms "longitudinal, transverse, upper, lower, front, rear, left, right, top, bottom, inner, outer" and the like refer to orientations or positional relationships based on those shown in the drawings, which are merely for convenience in describing the present invention and simplifying the description, and do not indicate or imply that the referred device or element must have a specific orientation, be constructed in a specific orientation, and be operated, and thus, should not be construed as limiting the present invention.

In addition, the indefinite articles "a", "an" and "an" preceding an apparatus or element of the invention are not intended to limit the number requirement (i.e., the number of occurrences) of the apparatus or element. Thus, "a" or "an" should be read to include one or at least one, and the singular form of a device or element also includes the plural form unless the number clearly indicates the singular form.

Please refer to fig. 1. FIG. 1 is a flow chart of a sintering control method 1 for a ceramic material according to an embodiment of the present invention. The sintering control method 1 of the ceramic material comprises the following steps: s1, preparing a uniform pore agent containing a uniform pore material; s2, mixing the pore-foaming agent and a ceramic slurry to form a green body; s3, sintering the green compact in an oxygen-free environment at a first temperature to form a ceramic blank; and S4, sintering the ceramic blank in an oxygen-containing environment at a second temperature to form a ceramic object. Wherein the second temperature is lower than the first temperature.

In step S1, the pore-forming material is a carbon-based material, an ore, a salt, a natural fiber or a polymer, and the carbon-based material can be carbon fiber, carbon nanotube, graphene or expanded graphite. Further, the carbon-based material may be mixed with natural organic fine powder, coal powder, limestone, dolomite, calcined zeolite, perlite, pumice, etc., or other pore-forming materials commonly used in the art to form pores, to form the pore-forming agent.

In step S1, the shape of the carbon-based material is spherical, plate-shaped, irregular, strip-shaped, or cubic. Wherein the size of the carbon-based material is 50nm to 400 μm; in a preferred embodiment, the carbon-based material has a size of 50nm to 100 μm. For example, in one embodiment, the carbon-based material is graphene in a flat sheet or planar film having a thickness of about 100nm and a length and width of about 100 μm. Or in another embodiment, the carbon-based material is a carbon nanotube with a diameter of about 50nm and a length of about 10 μm. However, the type, shape and size of the carbon-based material are not limited thereto, and those skilled in the art can reasonably substitute the type, shape and size according to the prior art, all of which are within the scope of the present invention and will not be described in detail in the specification.

In one embodiment, the ceramic material may be a high-silica silicate material, an aluminosilicate material, a fine ceramic material, a diatomite material, a corundum and silicon carbide material, cordierite, an aluminum titanate material, or other non-metallic inorganic materials. The ceramic material may also comprise so-called conventional ceramic material or new ceramic material. The new ceramic material also contains alumina, zirconia, magnesia, chromia, titania, tungsten carbide, titanium carbide, chromium carbide, silicon carbide, boron carbide, titanium nitride, silicon nitride or boron nitride. Also, the ceramic material may be ceramic powder or ceramic slurry.

Please refer to fig. 2. FIG. 2 is a flow chart of a sintering control method 1 for a ceramic material according to another embodiment of the present invention. In one embodiment, the step S2 of mixing the porogen with a ceramic material to form a green body further comprises the following sub-steps: s21, mixing the pore-forming agent and the ceramic slurry according to a predetermined ratio to form a mixed raw material. S22, printing the mixed raw material to form a green body by using the lamination manufacturing technique. The lamination manufacturing technique may be nozzle extrusion molding, stereolithography (surface exposure and laser), photocuring molding, adhesive injection molding, selective laser sintering or melt molding, slurry-layer casting (slurry-casting), or the like.

In one embodiment, the porogen and the ceramic slurry may be formed by mixing raw materials at a predetermined ratio and then sending the mixed raw materials out from a nozzle of a lamination forming machine to form a green compact with uniformly distributed porogen. Alternatively, the porogen and ceramic slurry are not mixed first, but are separately delivered by a nozzle to form a layered green body. Or the pore-foaming agent and the ceramic slurry are not mixed firstly, but are adjusted according to the parameter setting by the lamination manufacturing forming machine in a mixing cavity of the lamination manufacturing forming machine, and then the mixture is sent out by a nozzle to form a plurality of green bodies with different area pore-foaming agent proportions. In step S21, the porogen accounts for 0% to 50% of the predetermined ratio of the mixed raw material. In a more preferred embodiment, the porogen accounts for 0% to 35% of the predetermined proportion of the mixed raw material. For example, a green compact is formed in which the porogen content at one end is 0% and the porogen content at the other end is 35%.

Please refer to fig. 3. FIG. 3 is a flow chart of a sintering control method 1 for a ceramic material according to another embodiment of the present invention. In one embodiment, the step S3 of sintering the green body at a first temperature in an oxygen-free environment to form a ceramic green body further comprises the following sub-steps: s31, a stable gas is introduced into a predetermined environment to form an oxygen-free environment. S32, sintering the green body in an oxygen-free environment at a first temperature to form a ceramic blank.

In the prior art, the ceramic is formed only by one sintering, and the atmosphere of sintering air is not limited. In this stage of the present invention, the green body is first sintered to form a ceramic green body, and the green body is sintered in an oxygen-free environment. At the moment, the sintered rough blank is subjected to high-temperature sintering to generate microstructure change, the material shrinks, holes are reduced, a polycrystalline structure is established, the whole body is more compact, and the strength and the hardness of the material are improved. Due to the lack of oxygen in the environment to oxidize the porogen, the porogen remains in the blank.

In step S31, the stable gas is a non-oxygen gas which is stable and not easy to react, such as nitrogen, helium, neon, argon, krypton, xenon, etc. In step S32, the first temperature is higher than 600 ℃. In one embodiment, the first temperature is 1200 ℃ to 1800 ℃ which is suitable for sintering most ceramic materials. The first temperature needs to be below the melting point of the ceramic material used. However, the first temperature is not limited to the number. The first temperature is limited to a temperature within a range below the melting point of the ceramic material without damaging the porogen, and preferably the first temperature is selected to account for an optimal sintering temperature for the type of ceramic material. If the pore-forming material is a carbon-based material, the first temperature of 1200-1800 ℃ is an ideal first temperature without damaging the structure of the carbon-based material.

Please refer to fig. 4 and 5. FIG. 4 is a flow chart of a sintering control method 1 for a ceramic material according to another embodiment of the present invention. FIG. 5 illustrates the effect of carbon-based material ratio on porosity in one embodiment of the present invention. In one embodiment, step S4 further includes the following sub-steps: s41, air is introduced into a predetermined environment to form an oxygen-containing environment. And S42, sintering the ceramic rough blank in an oxygen-containing environment at a second temperature for 1 to 10 hours to form the ceramic object.

The predetermined environment described in step S3 and step S4 may be a sintering furnace, and step S3 and step S4 may be the same sintering furnace. In step S3, a non-oxygen gas is introduced into the sintering furnace and filled to form an oxygen-free environment. In step S4, air is introduced into the sintering furnace to form an oxygen-containing atmosphere. In step S4, in addition to the air, oxygen or any combination of gases containing oxygen may be introduced.

During this stage, the purpose of the second sintering is to high-temperature oxidize the porogen into a gas, e.g., carbon-based material into carbon monoxide or carbon dioxide. The oxidized gas of the pore-forming material escapes from the original remaining fine pores, so that new pores are left in the positions occupied by the carbon-based material. Because the second temperature is lower than the first temperature, the structure of the ceramic material is less affected by sintering at the second temperature (300 ℃ to 600 ℃), and material shrinkage and pore shrinkage are not easy to cause. Therefore, the shape and size of the holes can maintain the shape and size of the original carbon-based material, and the purpose of regulating and controlling the porosity and the pore shape of the ceramic article can be achieved. The time of this stage is not limited to 1 to 10 hours, and the shortest time for completely oxidizing the porogen should be selected according to the types of the ceramic material and the carbon-based material.

The first stage is high temperature oxygen-free sintering, and the second stage is low temperature oxygen-free sintering. The high temperature aims at manufacturing and forming ceramics with low porosity, compactness and high mechanical strength, and oxygen-free systems avoid the gasification of the pore-forming materials. In the second stage, the pore-forming material is gasified by oxygen to form pores of required size, shape and number, but the temperature is kept lower to avoid the formed pores being eliminated. Thus, the first temperature is a temperature suitable for sintering the ceramic slurry to compact and maintain the shape of the porogen, and the second temperature is a temperature suitable for vaporizing the porogen and preventing substantial compaction of the ceramic article. The specific temperature values in the present specification are only parameters in one embodiment, and should not be construed as limiting the present invention.

Wherein, when the pore-forming agent accounts for 0 to 50 percent of the predetermined proportion of the mixed raw materials, the porosity of the sintered ceramic article is 30 to 70 percent. As shown in fig. 5, the experimental conditions are that the pore-forming agent contains carbon-based material, the first temperature is 1200-1800 ℃, the second temperature is 300-600 ℃, the pore-forming agent and the ceramic material are mixed according to different proportions, and the porosity is measured after the sintering method of the present invention is performed. When the predetermined ratio (porogen content) of the porogen to the mixed raw material is 0% to 35%, the porosity (porosity) of the sintered ceramic article in step S4 is 30% to 60%. And the experimental chart shows that the standard error of the formed porosity is extremely small, which represents that the change of the porosity can be stably controlled by adjusting the preset proportion of the pore-foaming agent. Compared with the prior art, the method has the advantages that the porosity of the ceramic material sintered each time is different, the compactness and the mechanical strength are difficult to stabilize, the method can accurately control the porosity, and the ceramic object with consistent quality is produced.

In addition, the sintering control method of the ceramic material may also be applied to the sol-gel method, and the step S3 is not limited to a high temperature exceeding 600 ℃, and may be lower than 600 ℃.

Compared with the prior art, the sintering control method of the ceramic material of the invention mixes the carbon-based material as the pore-forming agent with the ceramic material. Then, by using two stages of sintering, oxygen-free air and oxygen-containing air are respectively introduced, and the corresponding sintering temperatures are controlled. Therefore, the obtained ceramic object has the advantages of compactness and mechanical strength after high-temperature sintering, and porosity loss after high-temperature sintering is avoided. Particularly, by adjusting the proportion, shape and size of the carbon-based material, the porosity and the shape of the holes in the ceramic object can be accurately regulated and controlled, so that the ceramic object can be accurately simulated and applied to various industrial requirements.

The above detailed description of the preferred embodiments is intended to more clearly illustrate the features and spirit of the present invention, and is not intended to limit the scope of the present invention by the preferred embodiments disclosed above. On the contrary, it is intended to cover various modifications and equivalent arrangements included within the scope of the claims. The scope of the claims is thus to be accorded the broadest interpretation so as to encompass all such modifications and equivalent arrangements as is within the scope of the appended claims.