[go: up one dir, main page]

CN110128159A - A kind of preparation method of rare earth oxide Al-base ceramic core - Google Patents

A kind of preparation method of rare earth oxide Al-base ceramic core Download PDF

Info

Publication number
CN110128159A
CN110128159A CN201910473577.7A CN201910473577A CN110128159A CN 110128159 A CN110128159 A CN 110128159A CN 201910473577 A CN201910473577 A CN 201910473577A CN 110128159 A CN110128159 A CN 110128159A
Authority
CN
China
Prior art keywords
ceramic core
preparation
rare earth
earth oxide
base ceramic
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.)
Pending
Application number
CN201910473577.7A
Other languages
Chinese (zh)
Inventor
高博
王伟
周衡
潘教庆
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.)
Anhui Qixin New Material Technology Co Ltd
Original Assignee
Anhui Qixin New Material 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 Anhui Qixin New Material Technology Co Ltd filed Critical Anhui Qixin New Material Technology Co Ltd
Priority to CN201910473577.7A priority Critical patent/CN110128159A/en
Publication of CN110128159A publication Critical patent/CN110128159A/en
Pending legal-status Critical Current

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
    • C04B35/10Shaped 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
    • C04B35/622Forming 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
    • C04B35/632Organic 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
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/71Ceramic products containing macroscopic reinforcing agents
    • C04B35/78Ceramic products containing macroscopic reinforcing agents containing non-metallic materials
    • C04B35/80Fibres, filaments, whiskers, platelets, or the like
    • 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
    • C04B2235/3205Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
    • C04B2235/3206Magnesium oxides or oxide-forming salts thereof
    • 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
    • C04B2235/3224Rare earth oxide or oxide forming salts thereof, e.g. scandium oxide
    • C04B2235/3227Lanthanum oxide or oxide-forming salts thereof
    • 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
    • C04B2235/50Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
    • C04B2235/52Constituents or additives characterised by their shapes
    • C04B2235/5208Fibers
    • C04B2235/5216Inorganic

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)
  • Chemical Kinetics & Catalysis (AREA)
  • Compositions Of Oxide Ceramics (AREA)

Abstract

A kind of preparation method of rare earth oxide Al-base ceramic core of the invention, belong to ceramic core manufacturing technology field, the chemical composition percentage of Al-base ceramic core material are as follows: 8%~10% ceramic fibre, 3%~5% silicate hydrolyzate liquid, 8%~10% silica solution, 60%~70% aluminium oxide, 1%~2% magnesia, 1%~2% lanthana and 10%~12% plasticizer, Al-base ceramic core intensity of the invention is high, and inoxidizability is strong.

Description

A kind of preparation method of rare earth oxide Al-base ceramic core
Technical field
The invention belongs to ceramic core manufacturing fields, systems a kind of system of rare earth oxide Al-base ceramic core Preparation Method.
Background technique
Oxide ceramics is various in style, and purposes is extremely wide, can be used as structural material, functional material and advanced fire proofed wood Material is used for many fields such as electronics, information, laser, infrared, computer, aerospace, atomic energy, chemical industry, metallurgy.
Currently, studying relatively broad aluminium oxide, oxidation silicon-base ceramic core, molten titanium is closed because core material does not have The good chemical reaction inertia of gold and core leach technics complexity is difficult to apply to titanium alloy fine casting field, and rare earth element is at high temperature With good reactionlessness, therefore a small amount of rare earth oxide is added i.e. in ceramic core, the high temperature and creep resistance of ceramic core can be improved Performance.
Through retrieving, the title of innovation and creation are as follows: a kind of rare earth coated aluminum oxide base ceramic core (application number: 201410224781.2 data of publication of application: 2014.10.01).This application discloses a kind of ceramics for being added to rare earth element Core has certain advantage in casting field using ceramic core prepared by the program, but the preparation method that the program is announced is inadequate Good, the intensity of ceramic core of preparation itself is low, and performance does not have the requirement in hot investment casting field, is easy to happen when in use crisp Disconnected, using effect is poor.
Summary of the invention
1. technical problems to be solved by the inivention
It is an object of the invention to solve the defect that existing ceramic core intensity is not high, inoxidizability is poor, provide a kind of dilute The preparation method of native oxide Al-base ceramic core, the ceramic core prepared using this method, intensity is high, and inoxidizability is strong.
2. technical solution
In order to achieve the above objectives, technical solution provided by the invention are as follows:
A kind of preparation method of rare earth oxide Al-base ceramic core of the invention, the chemical composition hundred of Al-base ceramic core material Divide ratio are as follows: 8%~10% ceramic fibre, 3%~5% silicate hydrolyzate liquid, 8%~10% silica solution, 60%~70% oxygen Change aluminium, 1%~2% magnesia, 1%~2% lanthana and 10%~12% plasticizer.
Preferably, aluminium oxide, magnesia and lanthana are nanometer grade powder.
Preferably, preparation method is to mix the material of ceramic core in proportion, heat, stirring to get mixture, into One step forms by a firing mixture injection molding high temperature.
Preferably, preparation method includes the following steps:
S100, mixing, by above-mentioned ceramic fibre, silica solution, aluminium oxide, magnesia, lanthana by the proportion into Row is mixed to get mixture;
S200, heating, heat mixture, and further stir to get ceramic powder;
S300, plasticising in the plasticizer to ceramic powder for adding the component, continue stirring and are no less than 15h that initial material is made;
S400, it glues by force, adds in a small amount of silicate hydrolyzate liquid to initial material, stir agglutination material;
Glue material is slowly injected into mold and rejects mixed air by S500, injection molding;
S600, pre-burning carry out heating pre-burning to the gluey material in mold using low temperature;
S700, it burns eventually, the first type core material after pre-burning carries out high temperature sintering, heat preservation and cooling and shaping.
Preferably, the detailed process of step S300 plasticising is that the addition of plasticizer is added using discontinuous, and every addition 1% is left Right plasticizer is just quickly stirred 15min, continues to add same amount of plasticizer after being stirred and be stirred, until It adds the desired amount of plasticizer and at the uniform velocity stirring is no less than 15h.
Preferably, the silicate hydrolyzate liquid that step S400 glues that by force detailed process is addition is added to from the edge of container Enter, the process of stirring is stirred from edge coils to centre.
Preferably, the detailed process of step S600 pre-burning is to carry out 600 °~800 ° under the protection of inert gas to add every mould Heat forms by a firing.
Preferably, the detailed process that step S700 is burnt eventually be by the first type core material after pre-burning be rapidly heated to 1350 °~ 1400 ° of progress high temperature sintering processing, carry out the no less than heat preservation of 5h after sintering, last natural cooling obtains rare earth oxide aluminium base Ceramic core.
3. beneficial effect
Using technical solution provided by the invention, compared with prior art, have the following beneficial effects:
(1) preparation method of a kind of rare earth oxide Al-base ceramic core of the invention, the chemical group of Al-base ceramic core material At percentage are as follows: 8%~10% ceramic fibre, 3%~5% silicate hydrolyzate liquid, 8%~10% silica solution, 60%~ 70% aluminium oxide, 1%~2% magnesia, 1%~2% lanthana and 10%~12% plasticizer, ceramic core of the invention Using aluminium oxide as substrate, solution pervasion is finally cooled into oxidation inside ceramic core and surface to aluminium oxide at high temperature Aluminium film has very high inoxidizability, so that the inoxidizability of ceramic core entirety improves, while wherein containing lanthana, improves The high temperature resistance of ceramic core.
(2) preparation method of a kind of rare earth oxide Al-base ceramic core of the invention, the detailed process of step S300 plasticising It is added for the addition of plasticizer using discontinuous, the plasticizer of every addition 1% or so is just quickly stirred 15min, and stirring is mixed Continue to add same amount of plasticizer after conjunction and be stirred, is no less than until adding the desired amount of plasticizer and at the uniform velocity stirring The process of 15h, this plasticising are slow and uniform, and plasticizer can be merged with material completely, so that the plasticity of entire ceramic core is high.
(3) preparation method of a kind of rare earth oxide Al-base ceramic core of the invention, step S400 glue by force detailed process and are The silicate hydrolyzate liquid of addition is added from the edge of container to be entered, and the process of stirring is stirred from edge coils to centre, this is strong Viscous process is slowly fade-in inside from outside, so that viscosity has gradient procedure, external viscosity is high, internal slightly lower, ensure that pottery The integrality of porcelain core is simultaneously but also the particle arrangement on surface is close, so that surface is more smooth.
Specific embodiment
To facilitate the understanding of the present invention, below with reference to several embodiments, still, the present invention can be with many different shapes Formula is realized, however it is not limited to embodiment described herein, on the contrary, purpose of providing these embodiments is makes to of the invention Disclosure is more thorough and comprehensive.
It should be noted that it can directly on the other element when element is referred to as " being fixedly arranged on " another element Or there may also be elements placed in the middle;When an element is considered as " connection " another element, it, which can be, is directly connected to To another element or it may be simultaneously present centering elements;Term as used herein " vertical ", " horizontal ", " left side ", " right side " and similar statement are for illustrative purposes only.
Unless otherwise defined, all technical and scientific terms used herein and belong to technical field of the invention The normally understood meaning of technical staff is identical;Term as used herein in the specification of the present invention is intended merely to description tool The purpose of the embodiment of body, it is not intended that in the limitation present invention;Term " and or " used herein includes one or more phases Any and all combinations of the listed item of pass.
A kind of preparation method of rare earth oxide Al-base ceramic core, the chemical composition percentage of Al-base ceramic core material are as follows: 8%~10% ceramic fibre, 3%~5% silicate hydrolyzate liquid, 8%~10% silica solution, 60%~70% aluminium oxide, 1% ~2% magnesia, 1%~2% lanthana and 10%~12% plasticizer, this Al-base ceramic core material composition in include Lanthana rare earth element the electric conductivity and high temperature resistance of ceramic core can be improved, while a large amount of aluminium oxide is as substrate The oxidation resistance that aluminum oxide film improves ceramic core is formed in core surface, plasticizer improves the plasticity energy of ceramic core Power, so that each material sufficiently merges, the viscosity of silicate hydrolyzate liquid improves the integral strength of ceramic core, while its fire resisting Property ceramic core is not burnt at high temperature, under silica solution and ceramic fibre high temperature occur reactive infiltration to inside formed calcium silicates Improve the intensity inside ceramic core.
Above-mentioned aluminium oxide, magnesia and lanthana is nanometer grade powder, is made using nanometer grade powder in subsequent system Standby is that can merge well and react with other materials, while the smaller density for improving ceramic core in gap between nanometer grade powder Increase intensity, surface is more smooth.
Preparation method is to mix the material of ceramic core in proportion, heat, stirring to get mixture, will further be mixed It closes object injection molding high temperature to form by a firing, the activity that preliminary heating improves molecule is carried out in mixing, accelerates fusion, so that material Mixing it is even closer, the ceramic core of subsequent preparation is more complete, and overall performance is consistent.
Above-mentioned preparation method includes the following steps:
S100, mixing, by above-mentioned ceramic fibre, silica solution, aluminium oxide, magnesia, lanthana by the proportion into Row is mixed to get mixture;
S200, heating, heat mixture, and further stir to get ceramic powder;
S300, plasticising in the plasticizer to ceramic powder for adding the component, continue stirring and are no less than 15h that initial material is made;
S400, it glues by force, adds in a small amount of silicate hydrolyzate liquid to initial material, stir agglutination material;
Glue material is slowly injected into mold and rejects mixed air by S500, injection molding;
S600, pre-burning carry out heating pre-burning to the gluey material in mold using low temperature;
S700, it burns eventually, the first type core material after pre-burning carries out high temperature sintering, heat preservation and cooling and shaping.
The detailed process of above-mentioned step S300 plasticising is that the addition of plasticizer is added using discontinuous, and every addition 1% is left Right plasticizer is just quickly stirred 15min, continues to add same amount of plasticizer after being stirred and be stirred, until It adds the desired amount of plasticizer and at the uniform velocity stirring is no less than 15h, if if disposable whole plasticizer is stirred again, add The local plasticity entered is high, and from being added, the farther away local plasticity in area is poor, while stirring can not make plasticizer and remaining material Fusion completely, overall effect is bad, and measures repeatedly several addition and stirring less using discontinuous, that is, may make plasticizer and its Remaining material is preferably merged and is reacted, and whole plasticity is guaranteed.
Above-mentioned step S400, which glues by force the silicate hydrolyzate liquid that detailed process is addition and adds from the edge of container, to be entered, The process of stirring is stirred from edge coils to centre, if silicate hydrolyzate liquid is added from centre, the viscosity ladder of the ceramic core Degree is internal strong external weak, and the intensity of ceramic core entirety is low, is easy face checking when high temperature is fired, also easy brittle failure when use, And say that silicate hydrolyzate liquid is added from edge and stirs to centre, adhesive strength outside is high internal weak, and core surface is not easy Cracking, whole also not easy to break, using effect is good.
The detailed process of above-mentioned step S600 pre-burning is to carry out 600 °~800 ° under the protection of inert gas to add every mould Heat forms by a firing, and the purpose of pre-burning is so that ceramic core is integrally formed, and intensity improves, and using inert gas shielding, avoids aluminium base The reaction of oxide, while but also moisture is evaporated.
The detailed process that above-mentioned step S700 is burnt eventually be by the first type core material after pre-burning be rapidly heated to 1350 °~ 1400 ° of progress high temperature sintering processing, carry out the no less than heat preservation of 5h after sintering, last natural cooling obtains rare earth oxide aluminium base Ceramic core, this step can make aluminium base oxide, and core surface forms film and carries out inoxidizability protection again, and 1350 °~ 1400 ° temperature range control avoid temperature it is excessively high so that ceramic core brittleness increase, after sintering heat preservation so that inside ceramic core Also it is able to maintain hot environment reaction, whole performance improves.
Embodiment 1
A kind of preparation method of rare earth oxide Al-base ceramic core of this embodiment, the chemical composition of Al-base ceramic core material Percentage are as follows: 10% ceramic fibre, 5% silicate hydrolyzate liquid, 10% silica solution, 60% aluminium oxide, 1% magnesia, 2% oxygen Change lanthanum and 12% plasticizer.
The compression strength of the ceramic core obtained after using the material of aforementioned proportion to be prepared is measured as 900Mpa, bending resistance Intensity is 300MPa.
Embodiment 2
A kind of preparation method of rare earth oxide Al-base ceramic core of this embodiment, the chemical composition of Al-base ceramic core material Percentage are as follows: 8% ceramic fibre, 4% silicate hydrolyzate liquid, 10% silica solution, 66% aluminium oxide, 1% magnesia, 1% oxygen Change lanthanum and 10% plasticizer.
The compression strength of the ceramic core obtained after using the material of aforementioned proportion to be prepared is measured as 930Mpa, bending resistance Intensity is 310MPa.
Embodiment 3
A kind of preparation method of rare earth oxide Al-base ceramic core of this embodiment, the chemical composition of Al-base ceramic core material Percentage are as follows: 9% ceramic fibre, 3% silicate hydrolyzate liquid, 8% silica solution, 70% aluminium oxide, 1% magnesia, 1% oxidation Lanthanum and 8% plasticizer.
The compression strength of the ceramic core obtained after using the material of aforementioned proportion to be prepared is measured as 1000Mpa, is resisted Curved intensity is 330MPa.
Certain embodiment of the invention above described embodiment only expresses, the description thereof is more specific and detailed, but simultaneously Limitations on the scope of the patent of the present invention therefore cannot be interpreted as;It should be pointed out that for those of ordinary skill in the art For, without departing from the inventive concept of the premise, various modifications and improvements can be made, these belong to guarantor of the invention Protect range;Therefore, the scope of protection of the patent of the invention shall be subject to the appended claims.

Claims (8)

1. a kind of preparation method of rare earth oxide Al-base ceramic core, it is characterised in that: the chemistry of the Al-base ceramic core material Percentage composition are as follows: 8%~10% ceramic fibre, 3%~5% silicate hydrolyzate liquid, 8%~10% silica solution, 60%~ 70% aluminium oxide, 1%~2% magnesia, 1%~2% lanthana and 10%~12% plasticizer.
2. a kind of preparation method of rare earth oxide Al-base ceramic core according to claim 1, it is characterised in that: the oxygen Changing aluminium, magnesia and lanthana is nanometer grade powder.
3. a kind of preparation method of rare earth oxide Al-base ceramic core according to claim 1, it is characterised in that: the system Preparation Method is to mix the material of ceramic core in proportion, heat, stirring to get mixture, further that mixture injection molding is high Temperature forms by a firing.
4. a kind of preparation method of rare earth oxide Al-base ceramic core according to claim 1, which is characterized in that the system Preparation Method includes the following steps:
S100, mixing are mixed above-mentioned ceramic fibre, silica solution, aluminium oxide, magnesia, lanthana by the proportion Conjunction obtains mixture;
S200, heating, heat mixture, and further stir to get ceramic powder;
S300, plasticising in the plasticizer to ceramic powder for adding the component, continue stirring and are no less than 15h that initial material is made;
S400, it glues by force, adds in a small amount of silicate hydrolyzate liquid to initial material, stir agglutination material;
Glue material is slowly injected into mold and rejects mixed air by S500, injection molding;
S600, pre-burning carry out heating pre-burning to the gluey material in mold using low temperature;
S700, it burns eventually, the first type core material after pre-burning carries out high temperature sintering, heat preservation and cooling and shaping.
5. a kind of preparation method of rare earth oxide Al-base ceramic core according to claim 4, is characterized in that: the step The detailed process of S300 plasticising is that the addition of plasticizer is added using discontinuous, and the plasticizer of every addition 1% or so just quickly stirs Mixing 15min is mixed, continues to add same amount of plasticizer after being stirred and be stirred, until adding the desired amount of plasticizer And at the uniform velocity stirring is no less than 15h.
6. a kind of preparation method of rare earth oxide Al-base ceramic core according to claim 4, is characterized in that: the step S400 glues by force silicate hydrolyzate liquid that detailed process be addition from the addition entrance of the edge of container, and the process of stirring is from edge spiral shell Rotation is stirred to centre.
7. a kind of preparation method of rare earth oxide Al-base ceramic core according to claim 4, is characterized in that: the step The detailed process of S600 pre-burning is to carry out 600 °~800 ° under the protection of inert gas to form by a firing every mould heating.
8. a kind of preparation method of rare earth oxide Al-base ceramic core according to claim 4, is characterized in that: the step The detailed process that S700 is burnt eventually is that the first type core material after pre-burning is rapidly heated to 1350 °~1400 ° progress high temperature sintering processing, The no less than heat preservation of 5h is carried out after sintering, last natural cooling obtains rare earth oxide Al-base ceramic core.
CN201910473577.7A 2019-06-01 2019-06-01 A kind of preparation method of rare earth oxide Al-base ceramic core Pending CN110128159A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910473577.7A CN110128159A (en) 2019-06-01 2019-06-01 A kind of preparation method of rare earth oxide Al-base ceramic core

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910473577.7A CN110128159A (en) 2019-06-01 2019-06-01 A kind of preparation method of rare earth oxide Al-base ceramic core

Publications (1)

Publication Number Publication Date
CN110128159A true CN110128159A (en) 2019-08-16

Family

ID=67579693

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910473577.7A Pending CN110128159A (en) 2019-06-01 2019-06-01 A kind of preparation method of rare earth oxide Al-base ceramic core

Country Status (1)

Country Link
CN (1) CN110128159A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110228996A (en) * 2019-06-26 2019-09-13 陕西博鼎快速精铸科技有限责任公司 One kind being based on the molding ceramic core preparation method of slurry direct write

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005093130A1 (en) * 2004-03-26 2005-10-06 The University Court Of The University Of St. Andrews Steam electrolysis
US20130089720A1 (en) * 2009-07-31 2013-04-11 General Electric Company Water based slurry compositions for making environmental barrier coatings and environmental barrier coatings comprising the same
CN103304227A (en) * 2013-07-01 2013-09-18 沈阳铸造研究所 Alumina-based ceramic core for directional solidification and preparation method thereof
CN104072112A (en) * 2014-05-24 2014-10-01 芜湖浙鑫新能源有限公司 Rare earth wrapped aluminum oxide-based ceramic forming core
CN105669198A (en) * 2016-01-16 2016-06-15 上海大学 Preparation method of lanthanum oxide-based ceramic core
CN106116533A (en) * 2016-06-23 2016-11-16 上海交通大学 The preparation method of high-porosity alumina base ceramic core
CN108585891A (en) * 2018-04-24 2018-09-28 芜湖浙鑫新能源有限公司 Rare-earth oxide modified ceramic core and preparation method thereof

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005093130A1 (en) * 2004-03-26 2005-10-06 The University Court Of The University Of St. Andrews Steam electrolysis
US20130089720A1 (en) * 2009-07-31 2013-04-11 General Electric Company Water based slurry compositions for making environmental barrier coatings and environmental barrier coatings comprising the same
CN103304227A (en) * 2013-07-01 2013-09-18 沈阳铸造研究所 Alumina-based ceramic core for directional solidification and preparation method thereof
CN104072112A (en) * 2014-05-24 2014-10-01 芜湖浙鑫新能源有限公司 Rare earth wrapped aluminum oxide-based ceramic forming core
CN105669198A (en) * 2016-01-16 2016-06-15 上海大学 Preparation method of lanthanum oxide-based ceramic core
CN106116533A (en) * 2016-06-23 2016-11-16 上海交通大学 The preparation method of high-porosity alumina base ceramic core
CN108585891A (en) * 2018-04-24 2018-09-28 芜湖浙鑫新能源有限公司 Rare-earth oxide modified ceramic core and preparation method thereof

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
刘晓军: "耐高温高比面积活性氧化铝的制备与性能研究", 《耐高温高比面积活性氧化铝的制备与性能研究 *
孙敏等著: "《熔模铸造》", 31 July 2015, 北京理工大学出版 *
庞强特: "《混凝土制品工艺学》", 31 January 1990, 武汉工业大学出版社 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110228996A (en) * 2019-06-26 2019-09-13 陕西博鼎快速精铸科技有限责任公司 One kind being based on the molding ceramic core preparation method of slurry direct write
CN110228996B (en) * 2019-06-26 2022-02-08 陕西博鼎快速精铸科技有限责任公司 Ceramic core preparation method based on slurry direct-writing forming

Similar Documents

Publication Publication Date Title
CN105835209B (en) A kind of Ceramic gel injection moulding forming method based on agarose
CN108913018A (en) A kind of high temperature resistant infrared low-emissivity coating and preparation method thereof
CN106898721B (en) A kind of lithium ion battery separator and preparation method thereof suitable for hot dry-pressing
CN110128116A (en) A kind of photocuring ceramic slurry and preparation method thereof
CN110128159A (en) A kind of preparation method of rare earth oxide Al-base ceramic core
CN114368972A (en) Visible light 3D printing photocurable ceramic paste, preparation method and printing method
CN109877324A (en) A kind of preparation method of kovar alloy Package boxes
CN117161401A (en) Quasi-continuous reticular titanium-based composite material based on additive manufacturing and method thereof
CN119566325A (en) A kind of alloy and preparation method thereof
CN103242044A (en) A kind of gel injection molding preparation method of BN/Si3N4 composite ceramics
CN113699410B (en) Impact-resistant titanium matrix composites with honeycomb-like structure based on two-step additive process
Topateş et al. Functionally graded Al2O3‐based ceramic systems by gel casting method
CN110976846A (en) Magnesium-based composite material for 3D printing, preparation method and 3D printing method thereof
CN117105645B (en) Corrosion-resistant brick for nitrogen kiln
CN110183234A (en) A kind of preparation method of rare earth oxide silicon based ceramic core
CN111747741A (en) 3D printing material, preparation method thereof and 3D printing method
CN106277724A (en) Laser selective sintering prepares the method for glass
CN106391997A (en) Preparation method of yttrium oxide composite paint for investment casting of titanium alloy
CN101850420B (en) A preparation method of tungsten-coated copper nanocomposite powder with controllable coating layer thickness
CN101898894B (en) Method for preparing β-Al2O3 precursor powder by spray drying with water as medium
JPH08134434A (en) Sealant for high temperature and its production
CN108439998A (en) A kind of preparation method of gel casting forming titanium nitride ceramic biscuit
CN109897400A (en) A kind of high-temperature-resistant insulating paint and preparation method thereof
Li et al. Effect of carbon dioxide temperature on adhesion of Na2SiO3 binder to silica sand surface: comparison of experimental data with molecular dynamics simulations
CN106398188A (en) Nylon composite powder material for selective laser sintering

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
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20190816