CN111704458B - Fine functional ceramic containing silicon dioxide nanocrystals and preparation method thereof - Google Patents

Fine functional ceramic containing silicon dioxide nanocrystals and preparation method thereof Download PDF

Info

Publication number
CN111704458B
CN111704458B CN202010445252.0A CN202010445252A CN111704458B CN 111704458 B CN111704458 B CN 111704458B CN 202010445252 A CN202010445252 A CN 202010445252A CN 111704458 B CN111704458 B CN 111704458B
Authority
CN
China
Prior art keywords
parts
silicon dioxide
functional ceramic
fine functional
deionized water
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
Application number
CN202010445252.0A
Other languages
Chinese (zh)
Other versions
CN111704458A (en
Inventor
林贵基
林宝明
罗桂
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Huaxia Fujian Vajra Technology Co ltd
Original Assignee
Huaxia Fujian Vajra Technology Co ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Huaxia Fujian Vajra Technology Co ltd filed Critical Huaxia Fujian Vajra Technology Co ltd
Priority to CN202010445252.0A priority Critical patent/CN111704458B/en
Publication of CN111704458A publication Critical patent/CN111704458A/en
Application granted granted Critical
Publication of CN111704458B publication Critical patent/CN111704458B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/48Shaped 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 zirconium or hafnium oxides, zirconates, zircon or hafnates
    • C04B35/486Fine ceramics
    • C04B35/488Composites
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/626Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
    • C04B35/63Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
    • C04B35/6303Inorganic additives
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3217Aluminum oxide or oxide forming salts thereof, e.g. bauxite, alpha-alumina
    • C04B2235/3218Aluminium (oxy)hydroxides, e.g. boehmite, gibbsite, alumina sol
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3231Refractory metal oxides, their mixed metal oxides, or oxide-forming salts thereof
    • C04B2235/3232Titanium oxides or titanates, e.g. rutile or anatase
    • C04B2235/3234Titanates, not containing zirconia
    • C04B2235/3236Alkaline earth titanates
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/34Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3418Silicon oxide, silicic acids, or oxide forming salts thereof, e.g. silica sol, fused silica, silica fume, cristobalite, quartz or flint
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/38Non-oxide ceramic constituents or additives
    • C04B2235/3817Carbides
    • C04B2235/3826Silicon carbides
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/48Organic compounds becoming part of a ceramic after heat treatment, e.g. carbonising phenol resins
    • C04B2235/483Si-containing organic compounds, e.g. silicone resins, (poly)silanes, (poly)siloxanes or (poly)silazanes
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/60Aspects relating to the preparation, properties or mechanical treatment of green bodies or pre-forms
    • C04B2235/602Making the green bodies or pre-forms by moulding
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/65Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
    • C04B2235/656Aspects 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
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/65Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
    • C04B2235/656Aspects 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
    • C04B2235/6567Treatment time
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/96Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Composite Materials (AREA)
  • Compositions Of Oxide Ceramics (AREA)

Abstract

The invention relates to the field of ceramic materials, in particular to fine functional ceramic containing silicon dioxide nanocrystals and a preparation method thereof. The fine functional ceramic comprises the following components, by weight, 8-10 parts of silicon dioxide nanocrystal powder; 25-30 parts of barium titanate; 8-12 parts of aluminum hydroxide; 45-55 parts of zirconium dioxide; 10-18 parts of silicon carbide; 4-8 parts of hexamethyldisilazane; 2-5 parts of concentrated ammonia water; 12-18 parts of deionized water. The surface of the silicon dioxide nanocrystal is modified by hexamethyldisilazane and concentrated ammonia water, so that the surface of the silicon dioxide nanocrystal exists in an uneven atomic step form, and conditions are provided for the connection of the surface of the silicon dioxide nanocrystal and other components, so that the strength of the integral structure of the fine functional ceramic is increased, the fine functional ceramic has better structural strength, and the fine functional ceramic has longer service life.

Description

Fine functional ceramic containing silicon dioxide nanocrystals and preparation method thereof
Technical Field
The invention relates to the field of ceramic materials, in particular to fine functional ceramic containing silicon dioxide nanocrystals and a preparation method thereof.
Background
Fine functional ceramics, broadly referred to as materials that utilize their non-mechanical properties primarily in their application, typically have one or more functions such as electrical, magnetic, optical, thermal, chemical, biological, etc., and some have coupling functions such as piezoelectric, piezomagnetic, thermoelectric, electro-optical, acousto-optical, magneto-optical, etc.
Specifically, piezoelectric ceramics, which is an emerging ceramic material, has been developed for over a hundred years. In the middle of the last century, the invention of PZT-based piezoelectric ceramics promoted the rapid development of electronic technology, so that various electronic products appeared in the front of us, and the piezoelectric ceramics, as an internal precise element, can convert electric energy into mechanical energy or mechanical energy into electric energy, and plays a key role in electronic products. In order to obtain high piezoelectric performance, doping modification is generally performed by using a soft additive, and although the method can make the piezoelectric ceramic performance active, the structural stability is poor, the service life is short, and the service life of an electronic product is finally affected.
Disclosure of Invention
In view of the above-mentioned drawbacks of the background art, the present invention provides a fine functional ceramic containing silica nanocrystals and a method for preparing the same.
The invention adopts the following technical scheme: a fine functional ceramic comprising silica nanocrystals, characterized in that: comprises the following components in parts by weight,
8-10 parts of silicon dioxide nanocrystal powder;
25-30 parts of barium titanate;
8-12 parts of aluminum hydroxide;
45-55 parts of zirconium dioxide;
10-18 parts of silicon carbide;
4-8 parts of hexamethyldisilazane;
2-5 parts of concentrated ammonia water;
12-18 parts of deionized water.
As a further improvement, the fine functional ceramic containing silica nanocrystals specifically comprises the following components in parts by weight, 10 parts of silica nanocrystal powder; 28 parts of barium titanate; 9 parts of aluminum hydroxide; 50 parts of zirconium dioxide; 4 parts of concentrated ammonia water; 15 parts of silicon carbide; 7 parts of hexamethyldisilazane; and 15 parts of deionized water.
As a further improvement, the silicon dioxide nano crystal powder comprises the following components in parts by weight, 8 parts of silicon dioxide nano crystal powder; 29 parts of barium titanate; 10 parts of aluminum hydroxide; 3 parts of concentrated ammonia water; 46 parts of zirconium dioxide; 15 parts of silicon carbide; 5 parts of hexamethyldisilazane; 16 parts of deionized water.
As a further improvement, the silicon dioxide nanocrystal powder is prepared from 65% of sodium silicate, 12% of absolute ethyl alcohol and 23% of deionized water.
The preparation method of the fine functional ceramic containing the silicon dioxide nanocrystals comprises the following steps:
s1: preparation of silica nanocrystal powder:
s2: pouring silicon dioxide nanocrystal powder, hexamethyldisilazane, concentrated ammonia water and water into a stirring container, and stirring for 5-10 min;
s3: filtering out water in the stirring container, and drying the silicon dioxide nanocrystal powder to obtain modified silicon dioxide nanocrystal powder;
s4: placing the modified silicon dioxide nanocrystal powder obtained in the step S3, barium titanate, aluminum hydroxide, zirconium dioxide, silicon carbide and deionized water into a stirring container for mixing to prepare mixed slurry;
s5: pouring the mixed slurry into a mold, and pressing and molding;
s6: opening the mold, taking out the green body formed by pressing, and putting the green body into a sintering furnace to sinter for 3-4 hours at the temperature of 1000-1150 ℃;
s7: and taking out the blank, naturally cooling, and polishing to obtain the fine functional ceramic.
As a further improvement of the above preparation method, the method for preparing the silica nanocrystal powder of step S1 includes the steps of,
s1-1: pouring sodium silicate, absolute ethyl alcohol and deionized water into a stirring container, stirring for 5-8 min, adding an ammonium chloride solution, and stirring for 15-20 min;
s1-2: heating the stirring container for 15-20 min at the temperature of 40-45 ℃ to obtain jelly;
s1-3: and drying the jelly, putting the jelly into an oven, and heating the jelly for 30-45 min at the temperature of 350-450 ℃ to obtain the silicon dioxide nanocrystal powder.
As a further improvement of the above preparation method, in step S1-1, the percentage of each component is 65% of sodium silicate, 12% of absolute ethyl alcohol, and 23% of deionized water.
As a further improvement of the above preparation method, in the step S2, in the step S2, water accounts for 8% of the total weight of the silica nanocrystal powder, hexamethyldisilazane, and concentrated ammonia water.
From the above description of the structure of the present invention, compared with the prior art, the present invention has the following advantages: according to the invention, the silicon dioxide nanocrystals are added into the components for preparing the fine functional ceramic, and the surface of the silicon dioxide nanocrystals is modified, so that the surface of the silicon dioxide nanocrystals exists in an uneven atomic step form, the contact surface of the chemical reaction of the silicon dioxide nanocrystals can be increased, and conditions are provided for the connection of the surface of the silicon dioxide nanocrystals and other components, thereby increasing the strength of the integral structure of the fine functional ceramic, and the polarity of the surface of the silicon dioxide can be weakened after the modification, the energy state of the surface of the silicon dioxide is reduced, the silicon dioxide nanocrystals are prevented from being agglomerated, the dispersibility of the silicon dioxide nanocrystals is improved, and the compatibility of the silicon dioxide nanocrystals with other substances (namely barium titanate and zirconium dioxide) is increased. Therefore, compared with the existing fine functional ceramic, the fine functional ceramic has better structural strength and longer service life.
Detailed Description
A fine functional ceramic containing silicon dioxide nano crystals comprises the following components in parts by weight: 8-10 parts of silicon dioxide nanocrystal powder; 25-30 parts of barium titanate; 8-12 parts of aluminum hydroxide; 45-55 parts of zirconium dioxide; 10-18 parts of silicon carbide; 4-8 parts of hexamethyldisilazane; 12-18 parts of deionized water. The silicon dioxide nanocrystal powder is prepared from 65% of sodium silicate, 12% of absolute ethyl alcohol and 23% of deionized water.
The preparation method of the fine functional ceramic containing the silicon dioxide nanocrystals comprises the following steps:
s1: the silica nanocrystal powder was prepared as follows:
s1-1: weighing 65% of sodium silicate, 12% of absolute ethyl alcohol and 23% of deionized water in percentage by weight, pouring the sodium silicate, the absolute ethyl alcohol and the deionized water into a stirring container, stirring for 5-8 min, adding an ammonium chloride solution, and stirring for 15-20 min, wherein the ammonium chloride solution accounts for 8% of the total amount of the components in the stirring container;
s1-2: heating the stirring container for 15-20 min at the temperature of 40-45 ℃ to obtain jelly;
s1-3: and drying the jelly, wherein the jelly can be placed on a tray in a drying mode and then placed in an oven for baking, specifically, the jelly can be baked at the temperature of 120 ℃ for 15-20 min, then the temperature of the oven is changed to the temperature of 350-450 ℃, the jelly is heated for 30-45 min, and preferably heated at the temperature of 420 ℃ for 40min, so that the silicon dioxide nanocrystal powder can be obtained.
S2: pouring the silicon dioxide nanocrystal powder, hexamethyldisilazane, concentrated ammonia water and water into a stirring container, and stirring for 5-10 min, wherein the water accounts for 8% of the total weight of the silicon dioxide nanocrystal powder, the hexamethyldisilazane and the concentrated ammonia water. In the process, hexamethyldisilazane is used for modifying the surface of silicon dioxide, and the silicon dioxide is an acidic oxide, so that alkaline concentrated ammonia water is added to neutralize the pH value of liquid in the stirring container, and the problem that the silicon dioxide nanocrystal powder cannot be modified due to the hydrolysis of a large amount of hexamethyldisilazane is avoided.
S3: and (3) filtering water in the stirring container, and drying the silicon dioxide nanocrystal powder, wherein the drying mode can be natural air drying or the drying mode is consistent with the drying mode of the jelly in the step S1-1, and the modified silicon dioxide nanocrystal powder can be obtained after drying. The modified silicon dioxide nanocrystal surface exists in an uneven atomic step form, so that the contact surface of chemical reaction can be increased, a condition is provided for the connection of the surface of the silicon dioxide nanocrystal and other inorganic matters, the polarity of the silicon dioxide surface can be weakened after modification, the energy state of the silicon dioxide surface is reduced, the silicon dioxide nanocrystal is prevented from being aggregated, and the dispersibility of the silicon dioxide nanocrystal and the compatibility of the silicon dioxide nanocrystal and other substances (namely barium titanate and zirconium dioxide) are improved.
S4: and (4) placing the modified silicon dioxide nanocrystal powder obtained in the step (S3), barium titanate, aluminum hydroxide, zirconium dioxide, silicon carbide and deionized water into a stirring container for mixing to prepare mixed slurry.
S5: and pouring the mixed slurry into a mold, and pressing and molding.
S6: and opening the mold, taking out the blank formed by pressing, and putting the blank into a sintering furnace to be sintered for 3-4 hours at the temperature of 1000-1150 ℃, particularly preferably 1100 ℃ for 3 hours.
S7: and taking out the blank, naturally cooling, and polishing to obtain the fine functional ceramic.
Referring to the above-described method for preparing a fine functional ceramic of silica nanocrystals, fine functional ceramics were prepared using examples of the components in different parts by weight as in the following table (1), respectively, in which silica nanocrystals, hexamethyldisilazane and concentrated ammonia water were not included in the components of example three, and thus were directly performed in accordance with steps S4 to S7.
Figure 786358DEST_PATH_IMAGE002
Watch (1)
The fine functional ceramics prepared in the above three examples were respectively tested for compressive strength and fracture toughness and again after 12 months, and the test results were compared as shown in the following table (2)
Figure DEST_PATH_IMAGE003
Watch (2)
Referring to the above table (2), it can be seen that the physical strength of the first and second examples is significantly higher than that of the third example, and the first and second examples are superior to each other in stability, while the first, second and third examples are different from each other in that the three components of silica nanocrystals, hexamethyldisilazane and concentrated ammonia water are absent, thereby showing that the fine functional ceramic of the present invention has better structural strength and longer service life than the existing functional ceramics.
The above description is only an embodiment of the present invention, but the design concept of the present invention is not limited thereto, and any insubstantial modifications made by using the design concept should fall within the scope of infringing the present invention.

Claims (4)

1. A fine functional ceramic comprising silica nanocrystals, characterized in that: the fine functional ceramic consists of the following components in parts by weight,
8-10 parts of silicon dioxide nanocrystal powder;
25-30 parts of barium titanate;
8-12 parts of aluminum hydroxide;
45-55 parts of zirconium dioxide;
10-18 parts of silicon carbide;
4-8 parts of hexamethyldisilazane;
2-5 parts of concentrated ammonia water;
12-18 parts of deionized water;
the manufacturing method of the fine functional ceramic comprises the following steps:
s1: preparing a silica nanocrystal powder comprising the steps of:
s1-1: weighing 65% of sodium silicate, 12% of absolute ethyl alcohol and 23% of deionized water by weight, pouring the sodium silicate, the absolute ethyl alcohol and the deionized water into a stirring container, stirring for 5-8 min, adding an ammonium chloride solution, and stirring for 15-20 min;
s1-2: heating the stirring container for 15-20 min at the temperature of 40-45 ℃ to obtain jelly;
s1-3: drying the jelly, putting the jelly into an oven, and heating the jelly for 30-45 min at the temperature of 350-450 ℃ to obtain silicon dioxide nanocrystal powder;
s2: pouring silicon dioxide nanocrystal powder, hexamethyldisilazane, concentrated ammonia water and deionized water into a stirring container, and stirring for 5-10 min;
s3: filtering out water in the stirring container, and drying the silicon dioxide nanocrystal powder to obtain modified silicon dioxide nanocrystal powder;
s4: placing the modified silicon dioxide nanocrystal powder obtained in the step S3, barium titanate, aluminum hydroxide, zirconium dioxide, silicon carbide and deionized water into a stirring container for mixing to prepare mixed slurry;
s5: pouring the mixed slurry into a mold, and pressing and molding;
s6: opening the mold, taking out the green body formed by pressing, and putting the green body into a sintering furnace to sinter for 3-4 hours at the temperature of 1000-1150 ℃;
s7: taking out the blank, naturally cooling, and polishing to obtain the fine functional ceramic.
2. The fine functional ceramic containing silica nanocrystals according to claim 1, wherein: the fine functional ceramic comprises the following components in parts by weight, 10 parts of silicon dioxide nanocrystal powder; 28 parts of barium titanate; 9 parts of aluminum hydroxide; 50 parts of zirconium dioxide; 15 parts of silicon carbide; 7 parts of hexamethyldisilazane; 4 parts of concentrated ammonia water; and 15 parts of deionized water.
3. The fine functional ceramic containing silica nanocrystals according to claim 1, wherein: the fine functional ceramic comprises the following components in parts by weight, 8 parts of silicon dioxide nanocrystal powder; 29 parts of barium titanate; 10 parts of aluminum hydroxide; 46 parts of zirconium dioxide; 15 parts of silicon carbide; 5 parts of hexamethyldisilazane; 3 parts of concentrated ammonia water; 16 parts of deionized water.
4. The fine functional ceramic containing silica nanocrystals according to claim 1, wherein: in step S2, deionized water accounts for 8% of the total weight of the silicon dioxide nanocrystal powder, hexamethyldisilazane, and concentrated ammonia water.
CN202010445252.0A 2020-05-24 2020-05-24 Fine functional ceramic containing silicon dioxide nanocrystals and preparation method thereof Active CN111704458B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202010445252.0A CN111704458B (en) 2020-05-24 2020-05-24 Fine functional ceramic containing silicon dioxide nanocrystals and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202010445252.0A CN111704458B (en) 2020-05-24 2020-05-24 Fine functional ceramic containing silicon dioxide nanocrystals and preparation method thereof

Publications (2)

Publication Number Publication Date
CN111704458A CN111704458A (en) 2020-09-25
CN111704458B true CN111704458B (en) 2022-05-27

Family

ID=72538066

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202010445252.0A Active CN111704458B (en) 2020-05-24 2020-05-24 Fine functional ceramic containing silicon dioxide nanocrystals and preparation method thereof

Country Status (1)

Country Link
CN (1) CN111704458B (en)

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB807454A (en) * 1954-05-06 1959-01-14 Monsanto Chemicals Surface-modified silica products and silicone rubbers containing the same
CN104312215A (en) * 2014-09-22 2015-01-28 太原理工大学 Silicon dioxide surface grafting modification method
CN107500752A (en) * 2017-08-03 2017-12-22 无锡南理工科技发展有限公司 A kind of nanometer piezoceramic material
CN107500751A (en) * 2017-08-03 2017-12-22 无锡南理工科技发展有限公司 The preparation method of nanometer piezoceramic material
CN108190896A (en) * 2018-01-20 2018-06-22 陕西科技大学 A kind of preparation method of order mesoporous nano silica microsphere
CN110003655A (en) * 2019-03-01 2019-07-12 雷洪军 A kind of preparation method of silicon rubber base aeroge composite insulation material
CN111040472A (en) * 2019-11-12 2020-04-21 中国石油天然气集团公司 Modified nano silicon dioxide and modification method thereof, anticorrosive paint and coating

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101906962B1 (en) * 2016-12-22 2018-10-11 주식회사 포스코 Annealing separating agent composition for grain oriented electrical steel sheet, grain oriented electrical steel sheet, and method for manufacturing grain oriented electrical steel sheet

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB807454A (en) * 1954-05-06 1959-01-14 Monsanto Chemicals Surface-modified silica products and silicone rubbers containing the same
CN104312215A (en) * 2014-09-22 2015-01-28 太原理工大学 Silicon dioxide surface grafting modification method
CN107500752A (en) * 2017-08-03 2017-12-22 无锡南理工科技发展有限公司 A kind of nanometer piezoceramic material
CN107500751A (en) * 2017-08-03 2017-12-22 无锡南理工科技发展有限公司 The preparation method of nanometer piezoceramic material
CN108190896A (en) * 2018-01-20 2018-06-22 陕西科技大学 A kind of preparation method of order mesoporous nano silica microsphere
CN110003655A (en) * 2019-03-01 2019-07-12 雷洪军 A kind of preparation method of silicon rubber base aeroge composite insulation material
CN111040472A (en) * 2019-11-12 2020-04-21 中国石油天然气集团公司 Modified nano silicon dioxide and modification method thereof, anticorrosive paint and coating

Also Published As

Publication number Publication date
CN111704458A (en) 2020-09-25

Similar Documents

Publication Publication Date Title
CN109608050B (en) High-frequency low-dielectric low-loss microcrystalline glass/ceramic LTCC substrate material and preparation method thereof
CN101880154B (en) Preparation method of nanometer cordierite-based ceramic dielectric material used for high-frequency chip inductor
CN106396414A (en) Low-temperature co-fired ceramic material and preparation method thereof
CN106587641A (en) Low-melting-point glass powder and laser-illumination glass ceramic made from low-melting-point glass powder
CN101648807A (en) Calcium barium zirconate titanate base piezoceramics and preparation method thereof
CN112194483B (en) High-strength calcium-magnesium-titanium microwave dielectric ceramic material and preparation method thereof
CN110483042B (en) Novel single-phase microwave dielectric ceramic material and preparation method thereof
CN102093054A (en) Faraday magnetic rotation transparent ceramic and preparation method thereof
CN104844204B (en) A kind of high dielectric microwave ceramic medium material, Preparation method and use
CN110357435B (en) High-strength high-modulus magnesium-aluminum-silicon microcrystalline glass material and preparation method thereof
CN111704458B (en) Fine functional ceramic containing silicon dioxide nanocrystals and preparation method thereof
CN101428856B (en) Process for producing silver tantalate niobate nano-powder
CN110407579B (en) Microwave dielectric material with ultrahigh Q value and preparation method thereof
CN102815941A (en) Rare-earth-ion-doped lanthanum gadolinium zirconate transparent ceramic material and preparation method thereof
CN116854472B (en) Microwave dielectric material and preparation method thereof
CN101337815A (en) Leadless piezoelectric ceramics and method for preparing the same
CN110372372B (en) Preparation method of sodium bismuth titanate-based lead-free piezoelectric ceramic with low dielectric loss at high temperature
CN1911860A (en) Preparation method of low temperature sintered electron ceramic material
CN110903078A (en) Ultralow dielectric constant LTCC microwave ceramic material and preparation method thereof
CN102815945A (en) Lanthanum gadolinium zirconate transparent ceramic material and preparation method thereof
CN113754436B (en) Preparation method of nanocrystalline laser-grade sesquioxide transparent ceramic
CN105060882A (en) Piezoceramic material and preparation method therefor
CN112811882B (en) High-stability sensor ceramic material and preparation method thereof
CN113004026B (en) LTCC microwave dielectric ceramic material and manufacturing method thereof
CN114835480A (en) Cordierite microwave dielectric material with ultralow dielectric constant and near-zero resonant frequency temperature coefficient 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