The present disclosure relates to the technical field of ceramic materials, and in particular relates to a low melting-point porous ceramic material and a method thereof.
Porous ceramic materials have characteristics of a large specific surface area, energy absorption, damping performance, etc. Specially processed porous ceramic materials have selective permeability to liquid, gas, and other substances to be widely used in various fields, such as vehicle exhaust treatment, chemical industry, machinery fields, and biomedical fields. At present, commercial porous ceramic materials mainly use Al2O3, SiC, ZrO2, and mullite as main raw materials. However, pore forming difficulties are caused due to these materials having a complex manufacturing process, a high sintering temperature, high energy consumption, high cost, or fire resistance mismatch between a pore forming agent and of a substrate. Therefore, the existing porous ceramic products have problems such as low mechanical strength, poor seismic resistance, poor damping performance, and have difficulty producing ideal through holes, resulting in a popularization and application of the existing porous ceramic products being severely limited. Therefore, suitable raw materials need to be found to effectively reduce the sintering temperature and to increase the porosity and the specific surface area of the porous ceramic materials, so as to promote wide application of the porous ceramic materials.
An objective of the present disclosure is to provide a low melting-point porous ceramic material to overcome the deficiencies of the existing techniques.
Another object of the present disclosure is to provide a method for preparing the low melting-point porous ceramic material.
A technical solution of the present disclosure is as follows:
A low melting-point porous ceramic material, a sintering temperature of the low melting-point porous ceramic material is 680-830° C., a porosity of the low melting-point porous ceramic material is 24-42%, raw materials of the low melting-point porous ceramic material comprise a binder (i.e., a temporary binder) and powder of raw materials, the powder of raw materials has a composition of components by weight as follows:
the powder of raw materials is prepared by mixing components of the composition, vitrifying, wet grinding, drying, and sieving.
In a preferred embodiment of the present disclosure, the binder is dextrin.
In a preferred embodiment of the present disclosure, the borate-glass sand and the Na2O powder pass through a 2000-mesh sieve.
In a preferred embodiment of the present disclosure, the purple clay powder, the quartz powder, and the LiO2 powder pass through a 1000-mesh sieve.
In a preferred embodiment of the present disclosure, a weight ratio of the powder of raw materials and the binder is 80-90:10-20.
In a preferred embodiment of the present disclosure, a weight ratio of the powder of raw material and the binder is 85:15.
In a preferred embodiment of the present disclosure, the powder of raw materials passes through a 5000-mesh sieve.
A method for preparing the low melting-point porous ceramic material, comprising:
In a preferred embodiment of the present disclosure, a temperature for the vitrifying is 800-900° C.
In a preferred embodiment of the present disclosure, a heating rate for the heating the unsintered body in the step 7 is 4-6° C. per minute, and a time for maintaining at the sintering temperature is 1.5-2.5 hours.
The present disclosure has the following advantages.
All of the raw materials in the present disclosure work synergistically, and the obtained product has advantages of a simple sintering process, a good mechanical strength, and generating pores without an addition of a pore forming agent, etc. The present disclosure effectively solves problems of fire resistance mismatch of the binder and the pore forming agent, poor heat dissipation performance, poor air permeability, etc., and a service life and holding power of the sintered porous ceramic material can be improved. A sintering temperature of the low melting-point porous ceramic material is only 680-780° C., a maximum porosity can reach 42% without the addition of the pore forming agent, and a good compressive strength, a good flexural strength, and a good hardness are maintained.
The technical solution of the present disclosure will be further described below in combination with the accompanying embodiments and drawings.
The weight ratios of the one or more components of the raw materials, the sintering temperature, and obtained technical effects in Embodiments 1-6 are shown in Table 1. A porous structure of the sintered low melting-point porous ceramic material obtained in Embodiment 1 are shown in
A specific manufacturing process of Comparison embodiments 1-5 is the same as the manufacturing process of Embodiments 1-6. Weight ratios of one or more components of raw materials, a sintering temperature, and obtained technical effects of Comparison embodiments 1-5 are shown in Table 1.
It can be seen from Table 1 that when an amount of the purple clay powder is less than 15%, pores of a sintered porous ceramic material change from through pores to closed pores, resulting in the porosity of the sintered porous ceramic material decreasing rapidly and not reflecting advantages of porous ceramics. When the amount of the purple clay powder is higher than 20%, the pores of the sintered porous ceramic material quickly overlap to become larger, causing the porosity of the sintered porous ceramic material to rapidly increase and mechanical properties of the sintered porous ceramic material to rapidly decrease. A strength of the sintered porous ceramic material is too low, resulting in an application range being greatly reduced and a service life rapidly decreasing.
When an amount of the borate-glass sand is less than 20%, the sintering temperature of the raw materials will reach 1100° C. The application range (such as ceramic grinding tools) will be narrowed due to the sintering temperature being too high, and morphology of abrasive particles of the sintered porous ceramic material will be damaged by excessively high sintering temperature (see Sha X, Yue W, Zhang H, et al. Thermal stability of polycrystalline diamond compact separated with born-loaded diamond particles [J]. Diamond and Related Materials. 2020, 104: 107753). When the amount of borate-glass sand is more than 55%, the sintering temperature of the raw materials still needs to be 680° C. and does not decrease following an increased content of the borate-glass sand. A temporary binder (i.e., a binder) used in a ceramic binder prepared by the present disclosure is the dextrin. Conventional temporary binders on the market, such as water glass, will react with the ceramic binder when mixing or produce pores after sintering, causing inherent pores of the purple clay powder to be destroyed and the ceramic binder to become dense.
This embodiment differs from Embodiment 1 in that the powder of raw materials and a water glass solution (as a binder instead of dextrin, a weight ratio of water and the water glass is 13.6:1) are mixed to even and then granulated to obtain the mixed raw material, wherein a weight ratio of the powder of raw materials and the water glass solution is 85:15. The mixed raw material is pressed into the desired shape and dried completely for 24 hours to obtain the unsintered body; the unsintered body is heated to 750° C. with the heating rate of 5° C. per minute and maintained at 750° C. for 2 hours to obtain sintered porous ceramics as shown in
The aforementioned embodiments are merely some embodiments of the present disclosure, and the scope of the disclosure is not limited thereto. Thus, it is intended that the present disclosure cover any modifications and variations of the presently presented embodiments provided they are made without departing from the appended claims and the specification of the present disclosure.
Number | Date | Country | Kind |
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202011586853.X | Dec 2020 | CN | national |
This application a continuation of International patent application PCT/CN2021/100348, filed on Jun. 16, 2021, which claims priority to Chinese patent application 202011586853.X, filed on Dec. 28, 2020. International patent application PCT/CN2021/100348 and Chinese patent application 202011586853.X are incorporated herein by reference.
Number | Date | Country | |
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Parent | PCT/CN2021/100348 | Jun 2021 | US |
Child | 18208822 | US |