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CN109336639A - A kind of porous ceramic film material and preparation method thereof - Google Patents

A kind of porous ceramic film material and preparation method thereof Download PDF

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Publication number
CN109336639A
CN109336639A CN201811442317.5A CN201811442317A CN109336639A CN 109336639 A CN109336639 A CN 109336639A CN 201811442317 A CN201811442317 A CN 201811442317A CN 109336639 A CN109336639 A CN 109336639A
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porous ceramic
ceramic film
film material
preparation
injection
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吴强德
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Jiaxing Chai Fuel Technology Co Ltd
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Jiaxing Chai Fuel Technology Co Ltd
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    • 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
    • C04B38/00Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
    • C04B38/06Porous 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
    • C04B38/063Preparing or treating the raw materials individually or as batches
    • C04B38/0635Compounding ingredients
    • C04B38/0645Burnable, meltable, sublimable materials
    • C04B38/0675Vegetable refuse; Cellulosic materials, e.g. wood chips, cork, peat, paper
    • 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
    • C04B35/10Shaped 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
    • 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
    • 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
    • C04B35/515Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
    • C04B35/58Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides
    • C04B35/584Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides based on silicon nitride
    • 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
    • C04B2235/3427Silicates other than clay, e.g. water glass

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

Abstract

The present invention relates to a kind of porous ceramic film materials and preparation method thereof, the following steps are included: silicate starting materials and pore creating material are mixed, premix is obtained, silicate starting materials include sodium metasilicate and other compounds, other compounds are at least one of oxide, nitride, carbide;Premix is dry, obtain silicate aggregate;Silicate aggregate is kneaded with binder, injection raw material is obtained, wherein by mass percentage, silicate aggregate is 50%~60%, binder is 40%~50%;It is injection moulded injection raw material to obtain biscuit;And biscuit is successively subjected to degumming process, calcination processing, obtain porous ceramic film material.The preparation method of above-mentioned porous ceramic film material; addition pore creating material method is combined with injection moulding; the porous ceramic film material porosity of preparation is high, aperture is controllable and has good mechanical property; due to using injection molding technique; compared to using dry pressuring forming process; production efficiency is improved significantly, and is suitble to large-scale production.

Description

A kind of porous ceramic film material and preparation method thereof
Technical field
The present invention relates to field of ceramic material preparation, more particularly to a kind of porous ceramic film material and preparation method thereof.
Background technique
Ceramic material is with natural or synthetic compound by one kind inorganic non-metallic material made of forming and high temperature sintering Material, purposes are very extensive.
The preparation method of common porous ceramic film material industrial at present mainly has addition pore creating material method, foam impregnation Method, foaming, injection moulding, granulation mass area method etc..But method made above has its limitation, such as addition pore creating material method The pore size distribution uniformity of porous ceramic film material obtained is poor, poor mechanical property, and production efficiency is low;What Polymeric sponge method obtained Article shape density is not easy to control;Foaming is higher to ingredient requirement, and process conditions are not easy to control;The acquisition of granulation mass area method The product porosity is lower.Therefore, how to prepare that porosity is high, aperture is controllable, good mechanical properties porous ceramic film materials are anxious Problem to be solved.
Summary of the invention
Based on this, it is necessary to provide and a kind of obtain that porosity is high, aperture is controllable, good mechanical properties porous ceramic film materials Preparation method and porous ceramic film material.
It there is a need to provide that a kind of porosity is high, aperture is controllable, good mechanical properties porous ceramic film materials.
It there is a need to provide a kind of high production efficiency, the electronic smoke atomizer long using the time.
A kind of preparation method of porous ceramic film material, comprising the following steps:
Silicate starting materials and pore creating material are mixed, premix are obtained, wherein the silicate starting materials include sodium metasilicate and its His compound, other compounds are at least one of oxide, nitride, carbide, and by mass percentage, sodium metasilicate is 25%~40%, other compounds are 45%~75%, and pore creating material is 5%~18%;
The premix is dry, obtain silicate aggregate;
The silicate aggregate is kneaded with the binder, obtains injection raw material, wherein by mass percentage Meter, silicate aggregate is 50%~60%, binder is 40%~50%;
It is injection moulded the injection raw material to obtain biscuit;
The biscuit is successively subjected to degumming process, calcination processing, obtains the porous ceramic film material.
The preparation method of above-mentioned porous ceramic film material combines with injection moulding addition pore creating material method, preparation it is more Hole ceramic material porosity is high, aperture is controllable and has good mechanical property, due to using injection molding technique, compared to adopting With dry pressuring forming process, production efficiency is improved significantly, and is suitble to large-scale production.
The pore creating material is at least one of sawdust, starch, graphite in one of the embodiments,.
The dry condition of the premix in one of the embodiments, are as follows: in 70 DEG C~110 DEG C dry 200min~ 400min。
In one of the embodiments, by mass percentage, the binder include: 60%~80% paraffin, 5% ~15% polypropylene, 5%~15% stearic acid and 5%~15% dibutyl phthalate.
The condition that the silicate aggregate and the binder are kneaded in one of the embodiments, are as follows: in 180 DEG C ~220 DEG C of mixing 3h~5h.
The injection moulding condition of the injection raw material in one of the embodiments, are as follows: injection temperature is 100 DEG C~160 ℃;Injection pressure is 50MPa~140MPa;Dwell pressure is 10MPa~30MPa.
The condition of the degumming process of the biscuit in one of the embodiments, are as follows: keep the temperature 3h at 200 DEG C~800 DEG C ~10h.
The condition of the calcination processing of the biscuit in one of the embodiments, are as follows: keep the temperature 1h at 800 DEG C~1600 DEG C ~4h.
A kind of porous ceramic film material is made using the preparation method of above-mentioned porous ceramic film material.
Application of the above-mentioned porous ceramic film material in electronic smoke atomizer.
Specific embodiment
It to facilitate the understanding of the present invention, below will be to invention is more fully described.This hair is given in embodiment Bright preferable scheme.But the invention can be realized in many different forms, however it is not limited to implementation described herein Example.It is made the disclosure of the present invention more thorough and comprehensive on the contrary, purpose of providing these embodiments is.
The porous ceramics preparation method of one embodiment, comprising the following steps:
Step S100: raw material is provided.
Raw material includes silicate starting materials, pore creating material and binder, and silicate starting materials include sodium metasilicate and other compounds, His compound is at least one of oxide, nitride, carbide.Using resourceful and free of contamination inorganic silicate material Expect the aggregate as porous ceramic film material, the condition of sintering is more mild, it can be achieved that under lower temperature, air atmosphere and normal pressure Sintering.
Particularly, oxide include aluminium oxide, zirconium oxide, silica, iron oxide, sodium oxide molybdena, potassium oxide, calcium oxide and Magnesia etc..
Particularly, nitride includes silicon nitride etc..
Particularly, carbide includes silicon carbide, boron carbide etc..
Particularly, other compound powders are broken to partial size is 60 μm~250 μm.Preferably, other compounds are ground Sieve.Specifically, by the ground standard screen for being sieved through 60 mesh, 200 mesh equal-specifications of other compounds.
Wherein, while sodium metasilicate is as raw material, also has the function of fluxing agent.Sodium metasilicate as raw material is used as simultaneously Fluxing agent can effectively reduce sintering temperature, and the glass phase with cementation is generated in high temperature, improve porous ceramic matrix The intensity of body.Particularly, sodium metasilicate can by anhydrous sodium metasilicate, sodium silicate nanahydrate (Na2SiO39H2O) or modulus be 1.5~ 3.5 sodium metasilicate provides.Wherein, modulus is the amount of the substance of silica and sodium oxide molybdena in waterglass (main component sodium metasilicate) The ratio between.Preferably, sodium metasilicate is provided by modulus for 2.6~2.8 sodium metasilicate.
Step S200: silicate starting materials and pore creating material are mixed, premix is obtained.
The specific steps of step S200 are as follows: pore creating material is sequentially added in other compounds, fluxing agent is mixed to get premix Material.Particularly, sodium metasilicate is added in form of an aqueous solutions, therefore obtained premix is wet feed.
Particularly, by mass percentage, by 25%~40% sodium metasilicate, 45%~75% other compounds, 5% ~18% pore creating material mixing, obtains premix.
Particularly, the time of silicate starting materials and pore creating material mixing is 0.5h~2h.
Preferably, dry-mixed using tumbling ball mill or planetary ball mill when silicate starting materials, pore creating material being mixed.It can manage Other modes mixing also can be used in solution, as long as guaranteeing that different materials are uniformly mixed, is such as stirred using blender or kneader It is dry-mixed.
Particularly, pore creating material is at least one of sawdust, starch, graphite.Using sawdust, starch, sucrose, wood-fibred and This large-sized complicated organic matter of short carbon fiber or inorganic matter can control finally formed more according to demand as pore creating material The aperture of hole ceramic material and porosity obtain being suitable for storing, conduct liquid and generate the intercommunicating pore structure of smog.
Particularly, the partial size of pore creating material is 10 μm~800 μm.
Preferably, using the pore creating material with different shape and structure, the connection hole shape of porous ceramic film material is obtained.Example Such as: using when there is the sawdust of strip to do pore creating material, the pore structure of obtained porous ceramic film material has a large amount of threadiness Structure;When doing pore creating material using spherical starch, the pore structure of obtained porous ceramic film material is mostly spheroid shape.
Preferably, the granularity for controlling pore creating material then can control the pore structure size of porous ceramic film material.
Preferably, the additional amount of pore creating material, the quantity and distribution density of the pore structure of controllable producing porous ceramic material are controlled. Therefore by adjusting type, the granularity, incorporation of pore creating material, different porous ceramic film materials can be prepared, to meet different product Demand.
Step S300: premix is dry, obtain silicate aggregate.
The dry condition of premix are as follows: in 70 DEG C~110 DEG C dry 200min~400min.
Preferably, the drying of premix carries out in drying box.
Step S400: silicate aggregate is kneaded with binder, obtains injection raw material.
Particularly, by mass percentage, by 50%~60% silicate aggregate and 40%~50% binder into Row is kneaded, and obtains injection raw material.
Particularly, by mass percentage, binder includes: 60%~80% paraffin (PW), poly- the third of 5%~15% Alkene (PP), 5%~15% stearic acid (SA) and 5%~15% dibutyl phthalate (DBP).Step S400 is specific Are as follows: at 180 DEG C~220 DEG C, after PP is melted completely, 170 DEG C~190 DEG C are cooled to, silicate aggregate, paraffin is added, is mixed 0.5h~1h is closed, stearic acid, DBP are continuously added, mixes 1h~2h.
Particularly, the condition of mixing is in 180 DEG C~220 DEG C mixing 3h~5h.
Particularly, it is kneaded and is carried out using kneading machine.
Step S500: it is injection moulded injection raw material to obtain biscuit.
Preferably, before step S500, injection raw material is stand-by through cooling, pelletizing.
It is furthermore preferred that the cooling of injection raw material uses natural cooling.It is furthermore preferred that injection raw material pelletizing to partial size is less than 5mm。
Particularly, pelletizing is carried out using crushing plant.Preferably, pelletizing technique uses jaw crushing equipment, roll crushing The machinery such as equipment or hammer crushing equipment are crushed.It is, of course, also possible to using other Mechanical Crushings, as long as guaranteeing broken rear former The Particle size requirements of material, for example use impact type crushing plant, circular cone type crushing plant, rotary type crushing plant etc..
Preferably, the injection moulding condition of raw material is injected are as follows: injection temperature is 100 DEG C~160 DEG C;Injection pressure is 50MPa~140MPa;Dwell pressure is 10MPa~30MPa.It is appreciated that injection technological parameter can with the difference of raw material proportioning It is adjusted.
Preferably, the injection moulding for injecting raw material is carried out in injection (mo(u)lding) machine, will inject raw material and injection (mo(u)lding) machine is added In hopper, corresponding injection technological parameter is set, is injection moulded to obtain biscuit.
Porous ceramic film material is prepared using injection molding technique, can the multiple biscuits of one-pass molding, both can guarantee product shrink Rate is smaller, and improves production efficiency, is suitble to large-scale industrial production.
Step S600: biscuit is successively subjected to degumming process, calcination processing, obtains porous ceramic film material.
Preferably, the condition of the degumming process of biscuit are as follows: 3h~10h is kept the temperature at 200 DEG C~800 DEG C.It is furthermore preferred that will Biscuit is warming up to 200 DEG C~800 DEG C with 1 DEG C/min~10 DEG C/min heating rate.
Particularly, the degumming process of biscuit divides the different temperatures stage to carry out, and different physics occurs in the different temperatures stage Chemical reaction.Specifically, the physical-chemical reaction that the different temperatures stage occurs include in conjunction with the sloughing of water, the sloughing of constitution water, The sloughing of pore creating material, the degumming of binder.Particularly, the soaking time of each temperature stage is 0.5h~2h.
Preferably, the condition of the calcination processing of biscuit are as follows: 1h~4h is kept the temperature at 800 DEG C~1600 DEG C.It is furthermore preferred that will Biscuit is warming up to 800 DEG C~1600 DEG C with 0.5 DEG C/min~5 DEG C/min heating rate.
Particularly, it after step S600, further comprises the steps of: porous ceramic film material natural cooling.
The preparation method of above-mentioned porous ceramic film material combines with injection moulding addition pore creating material method, preparation it is more Hole ceramic material porosity is high, aperture is controllable and has good mechanical property, due to using injection molding technique, compared to adopting With dry pressuring forming process, production efficiency is improved significantly, and is suitble to large-scale production.
The porous ceramic film material of one embodiment is prepared using the preparation method of above-mentioned porous ceramics.
Particularly, the porosity of porous ceramic film material is 35%~70%, and aperture is 200nm~2 μm.
Above-mentioned porous ceramic film material is in the application in electronic smoke atomizer.
It needs to store tobacco juice in electronic smoke atomizer and is atomized part tobacco juice every time, lead to the structure of electronic smoke atomizer Complex, production technology is complicated.Component for electronic smoke atomizer rationally, with higher porosity and some strength The preparation method of porous ceramic film material.
Particularly, tobacco juice is stored using porous ceramic film material in electronic smoke atomizer.Above-mentioned porous ceramic film material production Simple process, sintering temperature are low, and porosity with higher and good mechanical strength can be fine for storing tobacco juice Control smoke amount keep electronic smoke atomizer structure simple so simplifying the structure of electronic smoke atomizer, production technology letter Just, functional.
Embodiment 1:
After ground 80 mesh of alumina powder, 400g alumina powder is taken, 80 mesh~100 mesh sawdust 60g is added, in Ball grinding stirring mixing 30min in ball mill adds industrial waterglass (main component sodium metasilicate) 230g that modulus is 2.6, mixes Stirring 30min is closed, premix is obtained.
Premix is put in 80 DEG C of dry 400min in drying box, obtains dry silicate aggregate.
Kneading machine is preheated to 220 DEG C, polypropylene 20g is added in kneading machine, until being cooled to after polypropylene melts completely 170 DEG C, add silicate aggregate 400g, paraffin 300g, mixing 1h;Continuously add stearic acid 40g, dibutyl phthalate 40g, mixing 2h obtain injection raw material.
Raw material cooling will be injected, using crocodile formula crushing plant pelletizing.Injection (mo(u)lding) machine is added in injection raw material after pelletizing Hopper in, be injection moulded to obtain biscuit, injection temperature is 135 DEG C, injection pressure 140MPa, dwell pressure 10MPa.Element Under the size of base is preferably supplemented.
Biscuit is put into high-temperature pressure resistance furnace, is warming up to 200 DEG C with the heating rate of 5 DEG C/min, keeps the temperature 2h, then with Same rate is warming up to 300 DEG C, is warming up to 420 DEG C after keeping the temperature 1h, keeps the temperature 2h, then be warming up to 500 DEG C of guarantors with the rate of 2 DEG C/min Warm 1h, abjection combine water, constitution water, pore creating material and binder.Sample is warming up to 1400 DEG C of burnings again with the rate of 2 DEG C/min 1h is tied, the porous ceramic film material is obtained after furnace cooling.
Porous ceramic film material is subjected to porosity, bending strength, average pore size measurement.With this condition, porous ceramics material The porosity of material is 49.58%, bending strength 15.60Mpa, and average pore size is 1.250 μm.
Embodiment 2:
After zirconium oxide abrasive is crossed 60 meshes, 400g zirconium oxide is taken, 60 mesh~80 mesh sawdust 80g is added, in ball mill Middle ball grinding stirring mixing 40min adds the industrial waterglass 160g that modulus is 2.8, and 20min is mixed, obtains premix.
Premix is put in 100 DEG C of dry 300min in drying box, obtains dry silicate aggregate.
Kneading machine is preheated to 220 DEG C, polypropylene 40g is added in kneading machine, until being cooled to after polypropylene melts completely 170 DEG C, add silicate aggregate 400g, paraffin 280g, mixing 1h;Continuously add stearic acid 40g, dibutyl phthalate 40g, mixing 2h obtain injection raw material.
It will the cooling of injection raw material, pelletizing.Injection raw material after pelletizing is added in hopper, is injection moulded to obtain element Base, injection temperature are 140 DEG C, injection pressure 120MPa, dwell pressure 20MPa.
Biscuit is put into high-temperature pressure resistance furnace, is warming up to 200 DEG C with the heating rate of 2 DEG C/min, keeps the temperature 2h, then with Same rate is warming up to 300 DEG C, is warming up to 420 DEG C after keeping the temperature 1h, keeps the temperature 2h, then be warming up to 500 DEG C of guarantors with the rate of 2 DEG C/min Warm 1h, abjection combine water, constitution water, pore creating material and binder.Sample is warming up to 1200 DEG C of burnings again with the rate of 2 DEG C/min 1h is tied, the porous ceramic film material is obtained after furnace cooling.Porous ceramic film material is subjected to porosity, bending strength, average hole Diameter measurement.With this condition, the porosity of porous ceramic film material is 64.71%, bending strength 10.70Mpa, and average pore size is 1.885μm。
Embodiment 3:
After silicon nitride powder grinding is sieved with 100 mesh sieve, 400g silicon nitride powder is taken, the graphite 133g of 200 mesh is added, in ball mill Middle ball grinding stirring mixing 30min adds the industrial waterglass 355g that modulus is 1.5, and 30min is mixed, obtains premix.
Premix is put in 110 DEG C of dry 300min in drying box, obtains dry silicate aggregate.
Kneading machine is preheated to 220 DEG C, polypropylene 20g is added in kneading machine, until being cooled to after polypropylene melts completely 170 DEG C, add silicate aggregate 400g, paraffin 320g, mixing 1h;Continuously add stearic acid 20g, dibutyl phthalate 40g, mixing 2h obtain injection raw material.
It will the cooling of injection raw material, pelletizing.Injection raw material after pelletizing is added in hopper, is injection moulded to obtain element Base, injection temperature are 160 DEG C, injection pressure 140MPa, dwell pressure 30MPa.
Biscuit is put into high-temperature pressure resistance furnace, is warming up to 200 DEG C with the heating rate of 4 DEG C/min, keeps the temperature 2h, then with The heating rate of 2 DEG C/min is warming up to 420 DEG C, keeps the temperature 1h, then be warming up to 600 DEG C of heat preservation 1.5h with the rate of 2 DEG C/min, deviates from In conjunction with water, constitution water, graphite and binder;Sample is warming up to 1600 DEG C of sintering 4h again with the rate of 2 DEG C/min, it is cold with furnace But the porous ceramic film material is obtained afterwards.Porous ceramic film material is subjected to porosity, bending strength, average pore size measurement.Herein Under the conditions of, the porosity of porous ceramic film material is 36.95%, bending strength 19.60Mpa, average pore size 270nm.
Embodiment 4:
By ground 150 mesh of diatomite ore raw material, wherein diatomite ore raw material based on mass fraction, contains titanium dioxide Silicon 90%, aluminium oxide 6%, iron oxide 1%, sodium oxide molybdena 2.5%, other 0.5%.400g diatomite ore raw material is taken, is added 300 Purpose starch 40g, the ball grinding stirring mixing 30min in ball mill add the industrial waterglass 200g that modulus is 3.5, mixing 30min is stirred, premix is obtained.
Premix is put in 80 DEG C of dry 300min in drying box, obtains dry silicate aggregate.
Kneading machine is preheated to 200 DEG C, polypropylene 32 is added in kneading machine, until being cooled to after polypropylene melts completely 170 DEG C, add silicate aggregate 400g, paraffin 240g, mixing 1h;Continuously add stearic acid 26g, dibutyl phthalate 22g, mixing 2h obtain injection raw material.
It will the cooling of injection raw material, pelletizing.Injection raw material after pelletizing is added in hopper, is injection moulded to obtain element Base, injection temperature are 120 DEG C, injection pressure 80MPa, dwell pressure 10MPa.
Biscuit is put into high-temperature pressure resistance furnace, is warming up to 200 DEG C with the heating rate of 2 DEG C/min, keeps the temperature 2h, then with Same rate is warming up to 380 DEG C, is warming up to 420 DEG C after keeping the temperature 1h, keeps the temperature 1h, then be warming up to 500 DEG C of guarantors with the rate of 2 DEG C/min Warm 1h, abjection combine water, constitution water, starch and binder;Sample is warming up to 950 DEG C of sintering again with the rate of 2 DEG C/min 1h obtains the porous ceramic film material after furnace cooling.Porous ceramic film material is subjected to porosity, bending strength, average pore size Measurement.With this condition, the porosity of porous ceramic film material is 50.47%, bending strength 17.60Mpa, and average pore size is 475nm。
Embodiment 5:
By ground 250 mesh of feldspar-kaolin mixed mineral raw material, andesine-kaolin mixed mineral raw material with Mass fraction meter contains silica 65%, aluminium oxide 28%, iron oxide 0.5%, sodium oxide molybdena 5%, other 1.5%.Take 400g long The starch 12g of 300 mesh is added in stone-kaolin mixed mineral raw material, and ball grinding stirring mixing 30min, adds mould in ball mill The industrial waterglass 85g that number is 2.5 is mixed 30min, obtains premix.
Premix is put in 80 DEG C of dry 300min in drying box, obtains dry silicate aggregate.
Kneading machine is preheated to 180 DEG C, polypropylene 40g is added in kneading machine, until being cooled to after polypropylene melts completely 170 DEG C, dry feedstock 400g, paraffin 160g are added, stearic acid 40g, dibutyl phthalate 27g is added in mixing 1h, mixes Expect 2h, obtains injection raw material.
It will the cooling of injection raw material, pelletizing.Injection raw material after pelletizing is added in hopper, is injection moulded to obtain element Base, injection temperature are 100 DEG C, injection pressure 50MPa, dwell pressure 10MPa.
Biscuit is put into high-temperature pressure resistance furnace, is warming up to 200 DEG C with the heating rate of 2 DEG C/min, keeps the temperature 2h, then with Same rate is warming up to 380 DEG C, is warming up to 420 DEG C after keeping the temperature 40min, keeps the temperature 1h, then be warming up to 500 with the rate of 2 DEG C/min DEG C heat preservation 40min, abjection combine water, constitution water, starch and binder;Sample is warming up to 800 again with the rate of 2 DEG C/min DEG C sintering 2h, the porous ceramic film material is obtained after furnace cooling.Porous ceramic film material is subjected to porosity, bending strength, is put down Equal inside diameter measurement.With this condition, the porosity of porous ceramic film material is 44.82%, bending strength 13.35Mpa, average hole Diameter is 200nm.
Comparative example:
By ground 150 mesh of diatomite ore raw material, wherein diatomite ore raw material based on mass fraction, contains titanium dioxide Silicon 90%, aluminium oxide 6%, iron oxide 1%, sodium oxide molybdena (potassium) 2.5%, other 0.5%.100g diatomite ore raw material is taken, is added The starch 10g for entering 300 mesh, the ball grinding stirring mixing 30min in ball mill add the industrial waterglass 50g that modulus is 3.5, 30min is mixed, obtains wet feed, is fitted into cylindrical die, required green compact is pressed under 8MPa pressure.
Green compact is put into high-temperature pressure resistance furnace, 600 DEG C of heat preservation 2h are warming up to 2 DEG C/min rate, remove pore creating material And moisture;Sample is warming up to 800 DEG C of sintering 2h again with the rate of 2 DEG C/min, required porous ceramics is obtained after furnace cooling.It will The porous ceramics carries out porosity, bending strength, average pore size measurement.With this condition, the porosity of the porous ceramics is 72.12%, bending strength 9.60MPa, average pore size 621nm.
From Examples 1 to 5 it can be seen that porous ceramic film material prepared by the preparation method of porous ceramic film material of the invention Porosity is higher and intensity is preferable, and the porosity of porous ceramic film material obtained is 35%~70%, and bending strength is 10.7~ 20MPa, aperture are 200nm~2 μm.Meanwhile Examples 1 to 5, compared with comparative example, comparative example is using dry-pressing formed sample obtained Though product porosity is high, compression strength is very low, and requirement is not achieved in intensity.
Compare comparative example and embodiment 4, comparative example is identical as 4 silicate aggregate proportion of embodiment, subsequent forming agglomerant Skill is different.It can be seen that, due to containing moisture in raw material, demoulding is compared after molding when comparative example is formed using dry pressuring forming process Difficulty, easily causes deformation or damage at phenomena such as be easy to causeing sizing, falling off and compact strength is inadequate in transportational process.And Embodiment 4 is using injection moulding, and the sample of extrusion is due to binder rapid curing at low temperature, so that sample surfaces are smooth, no With die bonds, easy mold release, and sample has certain intensity, and situations such as deformation is damaged is less prone in transportational process.
It follows that in the subsequent sintering process, unbalance stress is formed using dry pressuring forming process, in green compact sintering process Easily there is phenomena such as cracking, destroy;As long as and being injection moulded injection temperature, the injection pressure kept in one injection forming process Power, dwell pressure and time, these technological parameters were constant, and porous ceramic film material performance obtained is stable, structure is uniform, reduced Cracking destruction phenomenon in sintering.
Each technical characteristic of embodiment described above can be combined arbitrarily, for simplicity of description, not to above-mentioned reality It applies all possible combination of each technical characteristic in example to be all described, as long as however, the combination of these technical characteristics is not deposited In contradiction, all should be considered as described in this specification.
The embodiments described above only express several embodiments of the present invention, and the description thereof is more specific and detailed, but simultaneously It cannot therefore be construed as limiting the scope of the patent.It should be pointed out that coming for those of ordinary skill in the art It says, without departing from the inventive concept of the premise, various modifications and improvements can be made, these belong to protection of the invention Range.Therefore, the scope of protection of the patent of the invention shall be subject to the appended claims.

Claims (9)

1. a kind of preparation method of porous ceramic film material, it is characterised in that: the following steps are included:
Silicate starting materials and pore creating material are mixed, premix is obtained, wherein the silicate starting materials include sodium metasilicate and other changes Object is closed, other compounds are at least one of oxide, nitride, carbide, by mass percentage, sodium metasilicate 25% ~40%, other compounds are 45%~75%, and pore creating material is 5%~18%;
The premix is dry, obtain silicate aggregate;
The silicate aggregate is kneaded with the binder, obtains injection raw material, wherein by mass percentage, silicon Hydrochlorate aggregate is 50%~60%, binder is 40%~50%;
It is injection moulded the injection raw material to obtain biscuit;
The biscuit is successively subjected to degumming process, calcination processing, obtains the porous ceramic film material.
2. the preparation method of porous ceramic film material according to claim 1, it is characterised in that: the pore creating material be sawdust, At least one of starch, graphite.
3. the preparation method of porous ceramic film material according to claim 1, it is characterised in that: the dry item of the premix Part are as follows: in 70 DEG C~110 DEG C dry 200min~400min.
4. the preparation method of porous ceramic film material according to claim 1, it is characterised in that: by mass percentage, institute State binder include 60%~80% paraffin, 5%~15% polypropylene, 5%~15% stearic acid and 5%~15% Dibutyl phthalate.
5. the preparation method of porous ceramic film material according to claim 1, it is characterised in that: the silicate aggregate and institute State the condition that binder is kneaded are as follows: in 180 DEG C~220 DEG C mixing 3h~5h.
6. the preparation method of porous ceramic film material according to claim 1, it is characterised in that: the injection of the injection raw material Condition of molding are as follows: injection temperature is 100 DEG C~160 DEG C;Injection pressure is 50MPa~140MPa;Dwell pressure be 10MPa~ 30MPa。
7. the preparation method of porous ceramic film material according to claim 1, it is characterised in that: the degumming process of the biscuit Condition are as follows: at 200 DEG C~800 DEG C keep the temperature 3h~10h.
8. the preparation method of porous ceramic film material according to claim 1, it is characterised in that: the calcination processing of the biscuit Condition are as follows: at 800 DEG C~1600 DEG C keep the temperature 1h~4h.
9. a kind of porous ceramic film material, it is characterised in that: using porous ceramic film material according to any one of claims 1 to 8 Preparation method is made.
CN201811442317.5A 2018-11-29 2018-11-29 A kind of porous ceramic film material and preparation method thereof Withdrawn CN109336639A (en)

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CN110467441A (en) * 2019-08-30 2019-11-19 东莞精陶科技有限公司 Porous ceramic substrate and preparation method thereof for atomizer
CN110742314A (en) * 2019-10-22 2020-02-04 深圳羽制科技有限公司 Electronic cigarette atomization core porous ceramic and preparation method thereof
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Publication number Priority date Publication date Assignee Title
CN110467441A (en) * 2019-08-30 2019-11-19 东莞精陶科技有限公司 Porous ceramic substrate and preparation method thereof for atomizer
CN110742314A (en) * 2019-10-22 2020-02-04 深圳羽制科技有限公司 Electronic cigarette atomization core porous ceramic and preparation method thereof
CN111153686A (en) * 2020-01-14 2020-05-15 东莞市陶陶新材料科技有限公司 Porous ceramic for electronic cigarette, atomizing core containing porous ceramic and preparation method of atomizing core
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WO2021163922A1 (en) * 2020-02-19 2021-08-26 昂纳自动化技术(深圳)有限公司 Electronic cigarette atomization assembly and manufacturing method therefor
CN112047753A (en) * 2020-08-21 2020-12-08 深圳市沁园春科技有限公司 Porous ceramic and preparation method and application thereof
CN112047753B (en) * 2020-08-21 2022-05-27 深圳市沁园春科技有限公司 Porous ceramic and preparation method and application thereof
CN115104765A (en) * 2021-03-19 2022-09-27 比亚迪股份有限公司 Atomizing core, preparation method of composite porous ceramic matrix for atomizing core and electronic atomizing device
RU2825752C1 (en) * 2021-06-04 2024-08-29 Шэньчжэнь Хуачэнда Пресижен Индастри Ко. Лтд. Porous spraying core configured to release negative ions, and method for production thereof
CN116265414A (en) * 2021-12-17 2023-06-20 东莞市陶陶新材料科技有限公司 A kind of porous ceramic material and its preparation method, and ceramic atomizing core
CN116477965A (en) * 2023-04-21 2023-07-25 深圳市博迪科技开发有限公司 A preparation method of a hydroxyapatite-based porous ceramic atomizing core embedded with a metal heating sheet

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