CN114920578B - Preparation method of porous anorthite/gehlenite complex-phase ceramic with low firing shrinkage rate - Google Patents
Preparation method of porous anorthite/gehlenite complex-phase ceramic with low firing shrinkage rate Download PDFInfo
- Publication number
- CN114920578B CN114920578B CN202210849814.7A CN202210849814A CN114920578B CN 114920578 B CN114920578 B CN 114920578B CN 202210849814 A CN202210849814 A CN 202210849814A CN 114920578 B CN114920578 B CN 114920578B
- Authority
- CN
- China
- Prior art keywords
- parts
- anorthite
- gehlenite
- porous
- preparation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B38/00—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
- C04B38/06—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof by burning-out added substances by burning natural expanding materials or by sublimating or melting out added substances
- C04B38/063—Preparing or treating the raw materials individually or as batches
- C04B38/0635—Compounding ingredients
- C04B38/0645—Burnable, meltable, sublimable materials
- C04B38/0675—Vegetable refuse; Cellulosic materials, e.g. wood chips, cork, peat, paper
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/10—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on aluminium oxide
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3205—Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
- C04B2235/3208—Calcium oxide or oxide-forming salts thereof, e.g. lime
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3418—Silicon oxide, silicic acids, or oxide forming salts thereof, e.g. silica sol, fused silica, silica fume, cristobalite, quartz or flint
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3427—Silicates other than clay, e.g. water glass
- C04B2235/3436—Alkaline earth metal silicates, e.g. barium silicate
- C04B2235/3445—Magnesium silicates, e.g. forsterite
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3427—Silicates other than clay, e.g. water glass
- C04B2235/3463—Alumino-silicates other than clay, e.g. mullite
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3427—Silicates other than clay, e.g. water glass
- C04B2235/3463—Alumino-silicates other than clay, e.g. mullite
- C04B2235/3472—Alkali metal alumino-silicates other than clay, e.g. spodumene, alkali feldspars such as albite or orthoclase, micas such as muscovite, zeolites such as natrolite
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3427—Silicates other than clay, e.g. water glass
- C04B2235/3463—Alumino-silicates other than clay, e.g. mullite
- C04B2235/3481—Alkaline earth metal alumino-silicates other than clay, e.g. cordierite, beryl, micas such as margarite, plagioclase feldspars such as anorthite, zeolites such as chabazite
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/349—Clays, e.g. bentonites, smectites such as montmorillonite, vermiculites or kaolines, e.g. illite, talc or sepiolite
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/36—Glass starting materials for making ceramics, e.g. silica glass
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/38—Non-oxide ceramic constituents or additives
- C04B2235/3817—Carbides
- C04B2235/3826—Silicon carbides
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/44—Metal salt constituents or additives chosen for the nature of the anions, e.g. hydrides or acetylacetonate
- C04B2235/447—Phosphates or phosphites, e.g. orthophosphate, hypophosphite
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/50—Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
- C04B2235/54—Particle size related information
- C04B2235/5418—Particle size related information expressed by the size of the particles or aggregates thereof
- C04B2235/5427—Particle size related information expressed by the size of the particles or aggregates thereof millimeter or submillimeter sized, i.e. larger than 0,1 mm
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/60—Aspects relating to the preparation, properties or mechanical treatment of green bodies or pre-forms
- C04B2235/602—Making the green bodies or pre-forms by moulding
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/60—Aspects relating to the preparation, properties or mechanical treatment of green bodies or pre-forms
- C04B2235/606—Drying
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/65—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
- C04B2235/656—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes characterised by specific heating conditions during heat treatment
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/65—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
- C04B2235/656—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes characterised by specific heating conditions during heat treatment
- C04B2235/6562—Heating rate
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/65—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
- C04B2235/656—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes characterised by specific heating conditions during heat treatment
- C04B2235/6567—Treatment time
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
- C04B2235/74—Physical characteristics
- C04B2235/77—Density
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
- C04B2235/96—Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
- C04B2235/96—Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
- C04B2235/9607—Thermal properties, e.g. thermal expansion coefficient
- C04B2235/9615—Linear firing shrinkage
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P40/00—Technologies relating to the processing of minerals
- Y02P40/60—Production of ceramic materials or ceramic elements, e.g. substitution of clay or shale by alternative raw materials, e.g. ashes
Abstract
The invention belongs to the technical field of ceramic preparation, and particularly relates to a preparation method of porous anorthite/gehlenite complex-phase ceramic with low firing shrinkage rate. Weighing ingredients according to a certain mass part ratio, wherein the ingredients comprise feldspar, quartz, waste glass powder, waste brick powder, kaolin, sawdust, sodium tripolyphosphate, polyacrylic acid, calcium carbonate, alumina, fused mullite powder, silicon carbide and talc, adding water into the ingredients for ball milling, drying slurry, manufacturing material particles, sieving with a 100-mesh sieve, and taking the material particles which are sieved with the 100-mesh sieve; molding the material particles by compression, and drying to obtain a blank body; heating the blank to 1170 ℃ to sinter, and then cooling to room temperature to prepare the anorthite/gehlenite complex-phase ceramic. The preparation method of the anorthite/gehlenite complex-phase ceramic adopts mineral materials as raw materials, has low cost and simple process, and is easy for industrial production.
Description
Technical Field
The invention belongs to the technical field of ceramic preparation, and particularly relates to a preparation method of porous anorthite/gehlenite complex-phase ceramic with low firing shrinkage rate.
Background
Anorthite has a high melting point, low thermal conductivity and thermal expansion coefficient and excellent thermal shock resistance. The porous ceramic taking anorthite as a main crystal phase has wide application prospects in the aspects of sewage treatment, sound absorption, high-temperature gas-solid separation, high-temperature heat insulation, gas sensors, catalyst carriers and the like. CN201510649256.X and CN201811276561.9 report that the porous anorthite ceramic prepared by a foam injection coagulation method has high porosity, but the process conditions are harsh and difficult to control; CN201810985266.4 reports a method for preparing porous ceramic by adding a pore-forming agent, the size and the shape of pores are controllable, the process is simple, and the pore distribution uniformity of the prepared anorthite sample is poor. The anorthite ceramic has low strength and is difficult to meet the requirements of some severe conditions; meanwhile, machining cracks are brought to products by mechanical processing after firing of ceramic products, so that control of firing precision is very important, and research on low firing shrinkage rate, particularly research on improvement of pore structure, density, volume shrinkage rate and mechanical property of porous ceramics through optimization of formula and process conditions, becomes increasingly important. The gehlenite has small density, small thermal expansion coefficient, low thermal conductivity and high strength and water resistance, for example, CN202010669868.6 mentions that the gehlenite is compounded with the gehlenite to generate complex phase ceramic, which can enhance the physical, mechanical and harsh environment-resistant service performance of the gehlenite.
The physical and chemical reactions of the materials in the sintering process of the solid ceramic blank change the microstructure and the phase, the viscosity of the glass phase is reduced in the high-temperature sintering process, the space between the solid materials is shortened, the contact area is increased, the bonding strength is increased, and the macroscopic expression is shrinkage, densification and strength increase. Therefore, the material formula and the sintering process have obvious influence on the microstructure and the macroscopic performance index of the ceramic material. In the production process of the porous ceramic, the reduction of the shrinkage rate and the improvement of the porosity rate are usually at the expense of the mechanical performance index, and the shrinkage rate, the porosity rate and the mechanical performance are difficult to be effectively unified. In the glass phase, the generation of the anorthite and the anorthite needs the processes of substance diffusion, crystal generation and growth, and the pores generated in the low-temperature decomposition process of the pore-forming agent form obstacles to the diffusion and crystallization processes of the substances. The problems need to continuously design and optimize the formula composition and the sintering process, and deeply research the evolution, generation and mutual law of phases. Only by optimizing the formula composition and balancing the competition process among the generation of the pores, anorthite and gehlenite can the microstructure be optimized to improve the firing shrinkage, so that the firing precision and the mechanical property of the ceramic product are improved simultaneously. However, no research on the firing of porous anorthite/gehlenite complex-phase ceramics with low firing shrinkage has been reported so far.
Disclosure of Invention
The purpose of the invention is: provides a preparation method of porous anorthite/gehlenite complex-phase ceramic with low sintering shrinkage. The preparation method ensures the strength of the porous anorthite/gehlenite complex-phase ceramic under the condition of meeting the requirements of pore structure, sintering shrinkage and density, so as to adapt to the mechanical requirements on the porous ceramic material in different application fields.
The preparation method of the porous anorthite/gehlenite complex-phase ceramic with low sintering shrinkage comprises the following steps:
(1) Weighing ingredients according to a certain mass part ratio, wherein the ingredients comprise feldspar, quartz, waste glass powder, waste brick powder, kaolin, sawdust, sodium tripolyphosphate, polyacrylic acid, calcium carbonate, alumina, fused mullite powder, silicon carbide and talc; adding water into the ingredients for ball milling, then drying the obtained slurry, finally preparing material particles, sieving the material particles by a 100-mesh sieve, and taking the material particles which are sieved by the 100-mesh sieve;
(2) Putting the material particles prepared in the step (1) into a die for compression molding, and drying to prepare a blank;
(3) And (3) heating the blank prepared in the step (2) to 1170 ℃, sintering, and cooling to room temperature to prepare the porous anorthite/gehlenite complex-phase ceramic with low sintering shrinkage.
Wherein:
the ingredients in the step (1) comprise the following raw materials in parts by weight: 11.59 parts of feldspar, 10.27 parts of quartz, 7.62 parts of waste glass powder, 6.95 parts of waste brick powder, 4.97 parts of kaolin, 1.32 parts of sawdust, 0.20 part of sodium tripolyphosphate, 0.32 part of polyacrylic acid, 23.90 parts of calcium carbonate, 18.92 parts of alumina, 9.96 to 18.11 parts of fused mullite powder, 0.33 to 0.66 part of silicon carbide and 3.32 parts of talc.
In the step (1), the raw material mixture consisting of 11.59 parts of feldspar, 10.27 parts of quartz, 7.62 parts of waste glass powder, 6.95 parts of waste brick powder, 4.97 parts of kaolin, 1.32 parts of sawdust, 0.20 part of sodium tripolyphosphate and 0.32 part of polyacrylic acid has the main chemical compositions of 3.98% of CaO and Al 2 O 3 12.1%、SiO 2 59.9% CO in carbonate 2 12.1%、B 2 O 3 4.24%、Na 2 O 1.81%、Fe 2 O 3 1.39% SO measured as sulphate 3 1.26%、K 2 O1.17%, mgO 0.74%, NO measured as nitrate 2 0.62%。
The mass part ratio of the ingredients to the water in the step (1) is 100.
And (2) adding water into the ingredients in the step (1) and carrying out ball milling for 1h at the speed of 400 r/min.
And (2) drying the obtained slurry in the step (1) at 110 ℃ for 2h.
The mode for manufacturing the material particles in the step (1) is manual granulation or mechanical granulation.
In the step (2), the forming pressure is 200MPa, the drying temperature is 110 ℃, and the drying time is 2h.
In the step (3), the temperature is increased to 1170 ℃ at the speed of 6 ℃/min for sintering, and the temperature is kept for 2h.
The cooling to room temperature in the step (3) is furnace cooling.
Wherein, the feldspar, the quartz and the waste glass powder in the ingredients provide guarantee for the generation of a glass phase in the high-temperature sintering process of the porous anorthite/gehlenite complex-phase ceramic. Calcium oxide generated by decomposing calcium carbonate reacts with alumina and silicon dioxide in materials in the firing process to generate anorthite/anorthite crystalline phase, the nucleation, growth and densification processes of the crystalline phase in the anorthite/anorthite complex-phase ceramic can be regulated and controlled in a high-temperature liquid phase by changing the using amounts of the electric-melting mullite powder and the silicon carbide, and the firing shrinkage rate, the pore structure, the density and the mechanical strength performance of the porous anorthite/anorthite complex-phase ceramic are optimized.
As a preferred technical scheme, the preparation method of the porous anorthite/gehlenite complex-phase ceramic with low firing shrinkage rate comprises the following steps:
(1) The materials are prepared according to the following mass portion: 11.59 parts of feldspar, 10.27 parts of quartz, 7.62 parts of waste glass powder, 6.95 parts of waste brick powder, 4.97 parts of kaolin, 1.32 parts of sawdust, 0.20 part of sodium tripolyphosphate, 0.32 part of polyacrylic acid, 23.90 parts of calcium carbonate, 18.92 parts of alumina, 9.96 to 18.11 parts of fused mullite powder, 0.33 to 0.66 part of silicon carbide and 3.32 parts of talc, wherein the main chemical composition of a raw material mixture consisting of 11.59 parts of feldspar, 10.27 parts of quartz, 7.62 parts of waste glass powder, 6.95 parts of waste brick powder, 4.97 parts of kaolin, 1.32 parts of sawdust, 0.20 part of sodium tripolyphosphate and 0.32 part of polyacrylic acid is 3.98% of CaO and Al 2 O 3 12.1%、 SiO 2 59.9%、CO measured as carbonate 2 12.1%、B 2 O 3 4.24%、Na 2 O 1.81%、Fe 2 O 3 1.39% SO in sulfate form 3 1.26%、K 2 O1.17%, mgO 0.74%, NO measured as nitrate 2 0.62%, adding water to enable the mass part ratio of the ingredients to the water to be 100:80, performing ball milling in a planetary ball mill at the speed of 400r/min for 1 hour, drying the slurry at 110 ℃ for 2 hours to prepare material particles, and taking the material particles with a 100-mesh sieve;
(2) Putting the material particles prepared in the step (1) into a mold, forming under 200MPa, and drying at 110 ℃ for 2 hours to prepare a blank;
(3) And (3) heating the blank prepared in the step (2) to 1170 ℃ at the speed of 6 ℃ per minute, preserving the heat for 2 hours, and cooling to room temperature to obtain the porous anorthite/gehlenite complex-phase ceramic with low firing shrinkage rate.
Compared with the prior art, the invention has the following beneficial effects:
(1) The preparation method of the porous anorthite/gehlenite complex phase ceramic with low sintering shrinkage rate, disclosed by the invention, has the advantages that the selected raw materials are mostly mineral materials, the cost is low, the technological process is consistent with the traditional ceramic production process, the process is simple, and the industrial production is easy to realize. The porous anorthite/gehlenite complex-phase ceramic produced by the method has low firing shrinkage, can be regulated and controlled by changing the formula composition, and meets the requirements of different application fields on firing shrinkage and firing precision; the porous anorthite/gehlenite complex-phase ceramic prepared by the method has high glass phase content, and the crystal in the blank is connected by taking the glass phase as a bonding phase after the anorthite/gehlenite is generated in the high-temperature sintering process, so that the strength of the porous anorthite/gehlenite complex-phase ceramic is ensured under the conditions of meeting the pore structure, the sintering shrinkage rate and the density, and the porous anorthite/gehlenite complex-phase ceramic is suitable for mechanical requirements on porous ceramic materials in different application fields.
(2) The firing shrinkage rate of the porous anorthite/gehlenite complex-phase ceramic produced by the method can be regulated according to a process formula, the firing precision requirement of the ceramic product can be met due to low firing shrinkage rate, and the basic requirements of application fields such as solid/gas separation, solid/liquid separation, sound insulation, heat preservation and insulation, catalyst carriers and the like can be met due to high mechanical strength.
Drawings
FIG. 1 is an XRD spectrum of the porous anorthite/gehlenite complex-phase ceramic prepared in example 1;
FIG. 2 is a SEM photograph of the porous anorthite/gehlenite composite ceramic prepared in example 1;
FIG. 3 is an XRD spectrum of the porous anorthite/gehlenite complex phase ceramic prepared in example 2;
FIG. 4 is a SEM photograph of the porous anorthite/gehlenite composite ceramic prepared in example 2;
FIG. 5 is an XRD spectrum of the porous anorthite/gehlenite complex-phase ceramic prepared in example 3;
FIG. 6 is a SEM photograph of the porous anorthite/gehlenite composite ceramic prepared in example 3;
FIG. 7 is an XRD spectrum of the porous anorthite/gehlenite complex-phase ceramic prepared in comparative example 1;
FIG. 8 is a SEM photograph of the porous anorthite/gehlenite composite ceramic prepared in comparative example 1;
FIG. 9 is an XRD spectrum of the porous anorthite/gehlenite complex phase ceramic prepared in the comparative example 2;
fig. 10 is a scanning electron microscope SEM photograph of the porous anorthite/gehlenite complex phase ceramic prepared in comparative example 2.
Detailed Description
The present invention is further described below with reference to examples.
Example 1
The preparation method of the porous anorthite/gehlenite complex-phase ceramic with low firing shrinkage rate described in the embodiment 1 comprises the following steps:
(1) The materials are prepared according to the following mass portion: 11.59 parts of feldspar, 10.27 parts of quartz, 7.62 parts of waste glass powder, 6.95 parts of waste brick powder, 4.97 parts of kaolin, 1.32 parts of sawdust, 0.20 part of sodium tripolyphosphate, 0.32 part of polyacrylic acid, 23.90 parts of calcium carbonate, 18.92 parts of alumina, 9.96 parts of electric-melting mullite powder, 0.66 part of silicon carbide and 3.32 parts of talc, and adding water, wherein the mass part ratio of the ingredients to the water is 100, the slurry is dried for 2 hours at 110 ℃ after being ball-milled for 1 hour at the speed of 400 revolutions per minute in a planetary ball mill, material particles are manually manufactured, and the material particles below a 100-mesh sieve are taken;
(2) Putting the material particles prepared in the step (1) into a mold, forming under 200MPa, and drying at 110 ℃ for 2 hours to prepare a blank;
(3) And (3) heating the blank prepared in the step (2) to 1170 ℃ at the speed of 6 ℃ per minute, preserving the heat for 2 hours, and cooling to room temperature to prepare the porous anorthite/gehlenite complex-phase ceramic with low firing shrinkage rate.
Wherein:
in the step (1), the raw material mixture consisting of 11.59 parts of feldspar, 10.27 parts of quartz, 7.62 parts of waste glass powder, 6.95 parts of waste brick powder, 4.97 parts of kaolin, 1.32 parts of sawdust, 0.20 part of sodium tripolyphosphate and 0.32 part of polyacrylic acid has the main chemical composition of 3.98% of CaO and Al 2 O 3 12.1%、SiO 2 59.9% CO in carbonate 2 12.1%、B 2 O 3 4.24%、Na 2 O 1.81%、Fe 2 O 3 1.39% SO in sulfate form 3 1.26%、K 2 O1.17%, mgO 0.74%, NO measured as nitrate 2 0.62%。
The waste brick powder is analyzed by X-ray diffraction, and the phases of the ceramic are anorthite (JCPDS No. 41-1486) and gehlenite (JCPDS No. 01-0982), as shown in figure 1. The microstructure of the ceramic is seen in scanning electron microscope SEM pictures, as shown in figure 2, the grain size is uniform, the sintering compactness is good, and a part of sintering necks have a small amount of air holes. Testing is carried out according to the steps of the boiling method mentioned in the national standard GB/T3810.1-2006 ceramic tile test method, and the porous anorthite/gehlenite complex phase ceramicThe density of the porcelain was 1.37 grams per cubic centimeter and the open porosity was 49.69%. The flexural strength of the ceramic measured by the three-point bending method was 19.36 MPa. The volume of the green body prepared by the step (2) is V 0 When the volume of the ceramic obtained in step (3) is V, the volume shrinkage ratio ((V) 0 -V)×100%/V 0 ) Comprises the following steps: 8.07 percent.
Example 2
The preparation method of the porous anorthite/gehlenite complex phase ceramic with low firing shrinkage rate described in this embodiment 2 includes the following steps:
(1) The materials are prepared according to the following mass portion: 11.59 parts of feldspar, 10.27 parts of quartz, 7.62 parts of waste glass powder, 6.95 parts of waste brick powder, 4.97 parts of kaolin, 1.32 parts of sawdust, 0.20 part of sodium tripolyphosphate, 0.32 part of polyacrylic acid, 23.90 parts of calcium carbonate, 18.92 parts of alumina, 18.11 parts of fused mullite powder, 0.66 part of silicon carbide and 3.32 parts of talc, and adding water, wherein the mass part ratio of the ingredients to the water is 100, and after ball milling for 1 hour at the speed of 400 revolutions per minute in a planetary ball mill, the slurry is dried for 2 hours at 110 degrees C, material particles are manually manufactured, and the material particles below a 100-mesh sieve are taken;
(2) Putting the material particles prepared in the step (1) into a mold, forming under 200MPa, and drying at 110 ℃ for 2 hours to prepare a blank;
(3) And (3) heating the blank prepared in the step (2) to 1170 ℃ at the speed of 6 ℃ per minute, preserving heat for 2 hours, and cooling to room temperature to obtain the porous anorthite/gehlenite complex-phase ceramic with low firing shrinkage rate.
Wherein:
in the step (1), the raw material mixture consisting of 11.59 parts of feldspar, 10.27 parts of quartz, 7.62 parts of waste glass powder, 6.95 parts of waste brick powder, 4.97 parts of kaolin, 1.32 parts of sawdust, 0.20 part of sodium tripolyphosphate and 0.32 part of polyacrylic acid has the main chemical composition of 3.98% of CaO and Al 2 O 3 12.1%、SiO 2 59.9% CO in carbonate 2 12.1%、B 2 O 3 4.24%、Na 2 O 1.81%、Fe 2 O 3 1.39% SO measured as sulphate 3 1.26%、K 2 O1.17%, mgO 0.74%, NO measured as nitrate 2 0.62%。
The waste brick powder is analyzed by X-ray diffraction, and the phases of the ceramics are anorthite (anorthite, JCPDS No. 41-1486) and gehlenite (JCPDS No. 01-0982), as shown in the attached figure 3. The microstructure of the ceramic is shown in Scanning Electron Microscope (SEM) picture, as shown in figure 4, the grain size is uniform, the sintering degree is moderate, and the sintering neck compactness is high. The porous anorthite/gehlenite complex-phase ceramic has the density of 1.35 g per cubic centimeter and the open porosity of 50.25 percent according to the test of the boiling method mentioned in the national standard GB/T3810.1-2006 ceramic tile test method. The flexural strength of the ceramic measured by the three-point bending method was 18.26 MPa. The volume of the blank prepared by the step (2) is V 0 When the volume of the ceramic obtained in step (3) is V, the volume shrinkage ratio ((V) 0 -V)×100%/V 0 ) Comprises the following steps: 4.56 percent.
Example 3
The preparation method of the porous anorthite/gehlenite complex phase ceramic with low firing shrinkage rate described in this embodiment 3 includes the following steps:
(1) The materials are prepared according to the following mass portion: 11.59 parts of feldspar, 10.27 parts of quartz, 7.62 parts of waste glass powder, 6.95 parts of waste brick powder, 4.97 parts of kaolin, 1.32 parts of sawdust, 0.20 part of sodium tripolyphosphate, 0.32 part of polyacrylic acid, 23.90 parts of calcium carbonate, 18.92 parts of alumina, 9.96 parts of electric-melting mullite powder, 0.33 part of silicon carbide and 3.32 parts of talcum, and adding water, wherein the mass part ratio of the materials to the water is 100, and after ball milling for 1 hour at the speed of 400 revolutions per minute in a planetary ball mill, drying the slurry at 110 ℃ for 2 hours, manually manufacturing granules, and taking the granules below a 100-mesh sieve;
(2) Putting the material particles prepared in the step (1) into a mold, forming under 200MPa, and drying at 110 ℃ for 2 hours to prepare a blank;
(3) And (3) heating the blank prepared in the step (2) to 1170 ℃ at the speed of 6 ℃ per minute, preserving the heat for 2 hours, and cooling to room temperature to obtain the porous anorthite/gehlenite complex-phase ceramic.
Wherein:
in the step (1), a raw material mixture consisting of 11.59 parts of feldspar, 10.27 parts of quartz, 7.62 parts of waste glass powder, 6.95 parts of waste brick powder, 4.97 parts of kaolin, 1.32 parts of sawdust, 0.20 part of sodium tripolyphosphate and 0.32 part of polyacrylic acid mainly comprises 3.98% of CaO and Al 2 O 3 12.1%、SiO 2 59.9% CO in carbonate 2 12.1%、B 2 O 3 4.24%、Na 2 O 1.81%、Fe 2 O 3 1.39% SO measured as sulphate 3 1.26%、K 2 O1.17%, mgO 0.74%, NO measured as nitrate 2 0.62%。
The phases of the ceramics are anorthite (Anorthite, JCPDS No. 41-1486) and gehlenite (JCPDS No. 01-0982) as shown in FIG. 5. The microstructure of the ceramic is seen in scanning electron microscope SEM pictures, as shown in figure 6, the holes are uniform and continuous, the grain size is small, and the sintering neck is compact and smooth. According to the test of the boiling method mentioned in the national standard GB/T3810.1-2006 ceramic tile test method, the density of the porous anorthite/gehlenite complex-phase ceramic is 1.32 g/cubic centimeter, and the open pore porosity is 51.02%. The flexural strength of the ceramic measured by the three-point bending method was 19.73 MPa. The volume of the blank prepared by the step (2) is V 0 When the volume of the ceramic obtained in step (3) is V, the volume shrinkage ratio ((V) 0 -V)×100%/V 0 ) Comprises the following steps: 4.31 percent.
Comparative example 1
The preparation method of the porous anorthite/gehlenite complex phase ceramic in the comparative example 1 is different from the preparation method in the example 1 in that only the mass part of the electric melting mullite powder is changed into 0, namely the electric melting mullite powder is not added, and the preparation method specifically comprises the following steps:
(1) The materials are prepared according to the following mass portion: 11.59 parts of feldspar, 10.27 parts of quartz, 7.62 parts of waste glass powder, 6.95 parts of waste brick powder, 4.97 parts of kaolin, 1.32 parts of sawdust, 0.20 part of sodium tripolyphosphate, 0.32 part of polyacrylic acid, 23.90 parts of calcium carbonate, 18.92 parts of alumina, 0.66 part of silicon carbide and 3.32 parts of talc, wherein water is added to ensure that the mass part ratio of the ingredients to the water is 100 percent, and after ball milling is carried out in a planetary ball mill at the speed of 400 revolutions per minute for 1 hour, slurry is dried for 2 hours at the temperature of 110 degrees C to manually manufacture material particles, and the material particles below a 100-mesh sieve are taken;
(2) Putting the material particles prepared in the step (1) into a mold, forming under 200MPa, and drying at 110 ℃ for 2 hours to prepare a blank;
(3) And (3) heating the blank prepared in the step (2) to 1170 ℃ at the speed of 6 ℃ per minute, preserving heat for 2 hours, and cooling to room temperature to obtain the porous anorthite/gehlenite complex-phase ceramic.
Wherein:
the raw material mixture consisting of 11.59 parts of feldspar, 10.27 parts of quartz, 7.62 parts of waste glass powder, 6.95 parts of waste brick powder, 4.97 parts of kaolin, 1.32 parts of sawdust, 0.20 part of sodium tripolyphosphate and 0.32 part of polyacrylic acid in the step (1) mainly comprises 3.98% of CaO and Al 2 O 3 12.1%、SiO 2 59.9% CO in carbonate 2 12.1%、B 2 O 3 4.24%、Na 2 O 1.81%、Fe 2 O 3 1.39% SO in sulfate form 3 1.26%、K 2 O1.17%, mgO 0.74%, NO measured as nitrate 2 0.62 percent. The phases of the ceramics are anorthite (anorthite, JCPDS No. 41-1486) and gehlenite (JCPDS No. 01-0982) as shown in FIG. 7. The microstructure of the ceramic is seen in SEM picture, as shown in FIG. 8, the crystal grain is in narrow strip shape, sintering degree is not enough, and sintering neck is not dense. The porous anorthite/gehlenite complex-phase ceramic has the density of 1.71 g/cubic centimeter and the open porosity of 31.02 percent according to the test of the boiling method mentioned in the national standard GB/T3810.1-2006 ceramic tile test method. The flexural strength of the ceramic measured by the three-point bending method was 16.83 MPa. The volume of the green body prepared by the step (2) is V 0 When the volume of the ceramic obtained in step (3) is V, the volume shrinkage ratio is ((V) 0 -V)×100%/V 0 ) Comprises the following steps: 30.43 percent.
Comparative example 2
The preparation method of the porous anorthite/gehlenite complex-phase ceramic in the comparative example 2 is different from the preparation method in the example 1 in that the mass part of the silicon carbide is only changed into 0, namely the silicon carbide is not added, and the preparation method specifically comprises the following steps:
(1) The materials are prepared according to the following mass portion ratio: 11.59 parts of feldspar, 10.27 parts of quartz, 7.62 parts of waste glass powder, 6.95 parts of waste brick powder, 4.97 parts of kaolin, 1.32 parts of sawdust, 0.20 part of sodium tripolyphosphate, 0.32 part of polyacrylic acid, 23.90 parts of calcium carbonate, 18.92 parts of alumina, 9.96 parts of electrically-fused mullite powder and 3.32 parts of talc, wherein water is added, the mass part ratio of the ingredients to the water is 100;
(2) Putting the material particles prepared in the step (1) into a mold, forming under 200MPa, and drying at 110 ℃ for 2 hours to prepare a blank;
(3) And (3) heating the blank prepared in the step (2) to 1170 ℃ at the speed of 6 ℃ per minute, preserving heat for 2 hours, and cooling to room temperature to obtain the porous anorthite/gehlenite complex-phase ceramic.
Wherein:
the raw material mixture consisting of 11.59 parts of feldspar, 10.27 parts of quartz, 7.62 parts of waste glass powder, 6.95 parts of waste brick powder, 4.97 parts of kaolin, 1.32 parts of sawdust, 0.20 part of sodium tripolyphosphate and 0.32 part of polyacrylic acid in the step (1) mainly comprises 3.98% of CaO and Al 2 O 3 12.1%、SiO 2 59.9% CO in carbonate 2 12.1%、B 2 O 3 4.24%、Na 2 O 1.81%、Fe 2 O 3 1.39% SO in sulfate form 3 1.26%、K 2 O1.17%, mgO 0.74%, NO measured as nitrate 2 0.62 percent. The phases of the ceramics are anorthite (anorthite, JCPDS No. 41-1486) and gehlenite (JCPDS No. 01-0982) as shown in FIG. 9. Microstructure of ceramicsAs shown in FIG. 10, the SEM photograph shows that the crystal grains grow well, the sintering necks are not dense, and a small number of holes are contained. The porous anorthite/gehlenite complex-phase ceramic has the density of 1.34 g per cubic centimeter and the open porosity of 51.49 percent according to the test of the boiling method mentioned in the national standard GB/T3810.1-2006 ceramic tile test method. The flexural strength of the ceramic measured by the three-point bending method was 14.27 MPa. The volume of the green body prepared by the step (2) is V 0 When the volume of the ceramic obtained in step (3) is V, the volume shrinkage ratio ((V) 0 -V)×100%/V 0 ) Comprises the following steps: 7.75 percent.
It can be seen from the comparative examples 1-2 that, when the porous anorthite/gehlenite complex-phase ceramic is prepared, when the other raw materials are unchanged, only the electric-melting mullite powder is not added in the comparative example 1, and the silicon carbide is not added in the comparative example 2, the volume shrinkage rate of the prepared porous anorthite/gehlenite complex-phase ceramic is greatly increased or the breaking strength is greatly reduced, and the volume shrinkage and the mechanical properties of the porous anorthite/gehlenite complex-phase ceramic cannot be balanced at the same time.
Claims (8)
1. A preparation method of porous anorthite/gehlenite multiphase ceramic with low sintering shrinkage is characterized in that: the method comprises the following steps:
(1) Weighing ingredients according to a certain mass part ratio, wherein the ingredients comprise feldspar, quartz, waste glass powder, waste brick powder, kaolin, sawdust, sodium tripolyphosphate, polyacrylic acid, calcium carbonate, alumina, fused mullite powder, silicon carbide and talc, adding water into the ingredients for ball milling, drying the obtained slurry, finally manufacturing material particles, sieving the material particles with a 100-mesh sieve, and taking the material particles which are sieved with the 100-mesh sieve;
(2) Putting the material particles prepared in the step (1) into a die for compression molding, and drying to prepare a blank;
(3) Heating the blank prepared in the step (2) to 1170 ℃ for sintering, and then cooling to room temperature to prepare the porous anorthite/gehlenite complex-phase ceramic with low sintering shrinkage;
wherein:
the ingredients in the step (1) comprise the following raw materials in parts by mass: 11.59 parts of feldspar, 10.27 parts of quartz, 7.62 parts of waste glass powder, 6.95 parts of waste brick powder, 4.97 parts of kaolin, 1.32 parts of sawdust, 0.20 part of sodium tripolyphosphate, 0.32 part of polyacrylic acid, 23.90 parts of calcium carbonate, 18.92 parts of alumina, 9.96 to 18.11 parts of fused mullite powder, 0.33 to 0.66 part of silicon carbide and 3.32 parts of talc.
2. The preparation method of the porous anorthite/gehlenite complex phase ceramic with low firing shrinkage rate as claimed in claim 1, wherein the ceramic comprises the following steps: the raw material mixture consisting of 11.59 parts of feldspar, 10.27 parts of quartz, 7.62 parts of waste glass powder, 6.95 parts of waste brick powder, 4.97 parts of kaolin, 1.32 parts of sawdust, 0.20 part of sodium tripolyphosphate and 0.32 part of polyacrylic acid in the step (1) mainly comprises 3.98% of CaO and Al 2 O 3 12.1%、SiO 2 59.9% CO in carbonate 2 12.1%、B 2 O 3 4.24%、Na 2 O 1.81%、Fe 2 O 3 1.39% SO in sulfate form 3 1.26%、K 2 O1.17%, mgO 0.74%, NO measured as nitrate 2 0.62%。
3. The preparation method of the porous anorthite/gehlenite complex-phase ceramic with low firing shrinkage rate as claimed in claim 1, wherein the preparation method comprises the following steps: the mass part ratio of the ingredients to the water in the step (1) is 100.
4. The preparation method of the porous anorthite/gehlenite complex-phase ceramic with low firing shrinkage rate as claimed in claim 1, wherein the preparation method comprises the following steps: in the step (1), water is added into the ingredients to perform ball milling for 1h at the speed of 400 r/min.
5. The preparation method of the porous anorthite/gehlenite complex phase ceramic with low firing shrinkage rate as claimed in claim 1, wherein the ceramic comprises the following steps: and (2) drying the slurry obtained in the step (1) at 110 ℃ for 2h.
6. The preparation method of the porous anorthite/gehlenite complex phase ceramic with low firing shrinkage rate as claimed in claim 1, wherein the ceramic comprises the following steps: in the step (2), the forming pressure is 200MPa, the drying temperature is 110 ℃, and the drying time is 2h.
7. The preparation method of the porous anorthite/gehlenite complex-phase ceramic with low firing shrinkage rate as claimed in claim 1, wherein the preparation method comprises the following steps: in the step (3), the temperature is increased to 1170 ℃ at the speed of 6 ℃/min for sintering, and the temperature is kept for 2h.
8. The preparation method of the porous anorthite/gehlenite complex phase ceramic with low firing shrinkage rate as claimed in claim 1, wherein the ceramic comprises the following steps: the cooling to room temperature in the step (3) is carried out along with furnace cooling.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202210849814.7A CN114920578B (en) | 2022-07-20 | 2022-07-20 | Preparation method of porous anorthite/gehlenite complex-phase ceramic with low firing shrinkage rate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202210849814.7A CN114920578B (en) | 2022-07-20 | 2022-07-20 | Preparation method of porous anorthite/gehlenite complex-phase ceramic with low firing shrinkage rate |
Publications (2)
Publication Number | Publication Date |
---|---|
CN114920578A CN114920578A (en) | 2022-08-19 |
CN114920578B true CN114920578B (en) | 2022-10-04 |
Family
ID=82815958
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202210849814.7A Active CN114920578B (en) | 2022-07-20 | 2022-07-20 | Preparation method of porous anorthite/gehlenite complex-phase ceramic with low firing shrinkage rate |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN114920578B (en) |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4808460A (en) * | 1987-06-02 | 1989-02-28 | Corning Glass Works | Laminated structures containing an inorganic corrugated or honeycomb member |
CN107628819B (en) * | 2016-07-18 | 2019-11-15 | 北方民族大学 | A method of preparing the porous material of the phase containing melilite using magnesium slag, flyash, carbide slag |
JP6873427B2 (en) * | 2017-03-28 | 2021-05-19 | 佐賀県 | Manufacturing method of porous ceramics |
CN111978100A (en) * | 2020-07-13 | 2020-11-24 | 南通大学 | Preparation and performance improvement method of anorthite/gehlenite complex phase ceramic |
-
2022
- 2022-07-20 CN CN202210849814.7A patent/CN114920578B/en active Active
Also Published As
Publication number | Publication date |
---|---|
CN114920578A (en) | 2022-08-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN106220224B (en) | High-temperature-resistant light heat-insulating material with double-hole structure and preparation method thereof | |
Zhao et al. | Transient liquid phase diffusion process for porous mullite ceramics with excellent mechanical properties | |
JP5661303B2 (en) | Composition for low-temperature fired porcelain and method for producing low-temperature fired porcelain | |
CN113121257B (en) | Ultra-light full-closed-cell foamed ceramic with compact surface and low-temperature firing method thereof | |
CN106747367B (en) | Preparation method of compact chromium oxide product with high thermal shock stability | |
CN105503236B (en) | The preparation method of nitride porous aluminium ceramic material | |
CN114031297A (en) | Cordierite-based porous glass ceramic and preparation method thereof | |
CN114920578B (en) | Preparation method of porous anorthite/gehlenite complex-phase ceramic with low firing shrinkage rate | |
CN106431435A (en) | Porous periclase-forsterite multiphase material and preparation method thereof | |
JP6873427B2 (en) | Manufacturing method of porous ceramics | |
KR101866319B1 (en) | Process for manufacturing high density slip-cast fused silica bodies | |
CN115819109B (en) | Fully-closed-pore foamed ceramic and low-temperature firing method thereof | |
CN108546131B (en) | Preparation method of silicon nitride porous ceramic | |
CN108911715B (en) | Closed-cell foamed ceramic with hard compact shell and preparation method thereof | |
JP3839537B2 (en) | Production method of opaque quartz glass containing fine bubbles | |
CN106830906B (en) | Densification method of low-gradient-difference chromium oxide product | |
CN106348773B (en) | A kind of anti-lithium electric material erosion fire-clay crucible adding SiAlON-AlN-TiN | |
CN106518139B (en) | A kind of preparation method of insulating fire brick | |
KR101343808B1 (en) | Composite for low temperature sinterable porcelain and manufacturing method of low temperature sinterable porcelain | |
Hanna et al. | Oxidation resistance, compressive strength and thermal shock resistance of SiC ceramics prepared by two processing routes | |
KR101110363B1 (en) | Sintered lithium oxide-aluminum oxide-silicon oxide having low thermal expansion and manufacturing method of the same | |
CN111111320A (en) | Magnesium oxide-based filter with multi-pore structure and preparation method thereof | |
CN108558412B (en) | Preparation method of porous silicon nitride ceramic material | |
CN114790084B (en) | Porous microcrystalline glass and preparation method thereof | |
CN115180932B (en) | Mullite porous ceramic based on high-sodium industrial alumina in-situ synthesis and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
PE01 | Entry into force of the registration of the contract for pledge of patent right |
Denomination of invention: Preparation method of porous Anorthite/anorthite composite ceramics with low firing shrinkage Effective date of registration: 20230719 Granted publication date: 20221004 Pledgee: Zibo Zichuan District sub branch of China Post Savings Bank Co.,Ltd. Pledgor: ZIBO JINSHIWANG TECHNOLOGY CERAMIC GROUP CO.,LTD. Registration number: Y2023980049131 |
|
PE01 | Entry into force of the registration of the contract for pledge of patent right |