CN110015902A - A kind of low temperature burning glazed tiles additive - Google Patents

A kind of low temperature burning glazed tiles additive Download PDF

Info

Publication number
CN110015902A
CN110015902A CN201910326018.3A CN201910326018A CN110015902A CN 110015902 A CN110015902 A CN 110015902A CN 201910326018 A CN201910326018 A CN 201910326018A CN 110015902 A CN110015902 A CN 110015902A
Authority
CN
China
Prior art keywords
mass ratio
parts
glazed tiles
mixing
low temperature
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
CN201910326018.3A
Other languages
Chinese (zh)
Inventor
赵金城
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.)
Foshan Botemei Ceramics Co Ltd
Original Assignee
Foshan Botemei Ceramics 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 Foshan Botemei Ceramics Co Ltd filed Critical Foshan Botemei Ceramics Co Ltd
Priority to CN201910326018.3A priority Critical patent/CN110015902A/en
Publication of CN110015902A publication Critical patent/CN110015902A/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
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/62204Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products using waste materials or refuse
    • 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
    • C04B35/62605Treating the starting powders individually or as mixtures
    • 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
    • C04B35/64Burning or sintering processes
    • 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
    • C04B2235/3201Alkali metal 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
    • C04B2235/3205Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
    • C04B2235/3208Calcium oxide or oxide-forming salts thereof, e.g. lime
    • 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
    • C04B2235/3215Barium 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
    • C04B2235/3217Aluminum oxide or oxide forming salts thereof, e.g. bauxite, alpha-alumina
    • 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
    • C04B2235/3229Cerium 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
    • C04B2235/3231Refractory metal oxides, their mixed metal oxides, or oxide-forming salts thereof
    • C04B2235/3232Titanium oxides or titanates, e.g. rutile or anatase
    • 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
    • C04B2235/327Iron group oxides, their mixed metal oxides, or oxide-forming salts thereof
    • C04B2235/3272Iron oxides or oxide forming salts thereof, e.g. hematite, magnetite
    • 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
    • C04B2235/3284Zinc oxides, zincates, cadmium oxides, cadmiates, mercury oxides, mercurates 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
    • C04B2235/30Constituents 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
    • 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
    • C04B2235/3463Alumino-silicates other than clay, e.g. mullite
    • 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
    • C04B2235/349Clays, e.g. bentonites, smectites such as montmorillonite, vermiculites or kaolines, e.g. illite, talc or sepiolite
    • 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
    • C04B2235/42Non metallic elements added as constituents or additives, e.g. sulfur, phosphor, selenium or tellurium
    • C04B2235/422Carbon
    • C04B2235/425Graphite
    • 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
    • C04B2235/5284Hollow fibers, e.g. nanotubes
    • C04B2235/5288Carbon nanotubes

Landscapes

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

Abstract

The invention discloses the preparation methods that a kind of low temperature burns glazed tiles additive, belong to glazed tiles additive agent field.The present invention is activated using pug and magnetic iron ore, blast furnace titaniferous slag grinding, add sulfuric acid solution, improve interstructural compactness, the isocyanate prepolymer composition contained in made crosslinker component can be combined into the siloxanes with bridge crosslinking structure with silane coupling agent ingredient, hybrid inorganic-organic synergistic effect is provided, and molecule is filled, promote the consistency after being sintered inside glazed tiles;Matrix fillers containing white carbon black, graphene, microcrystalline cellulose are ultrasonically treated, and are blended with the carbon nanotube of addition, carbon nano-tube network network diagram collection activity hard constituents, it is acted in conjunction with the storage oxygen and aiding combustion of metallic cerium, fuel efficiency is promoted, firing time is reduced, improves consistency.The present invention solves sintering temperature height when sintering glazed tiles additive therefor application at present, and firing time is long, the low problem of structural compactness.

Description

A kind of low temperature burning glazed tiles additive
Technical field
The invention belongs to glazed tiles additive preparation field, in particular to a kind of low temperature burns the preparation side of glazed tiles additive Method.
Background technique
Glazed tiles are an ancient, traditional ceramic materials.With the development of tourist industry, demand of the people for glazed tiles And it is more and more, it is required to be also higher and higher.Glazed tiles are crushed by screening, high pressure using high-quality ore raw materials Molding, high temperature are fired.It is high with intensity, flatness is good, water absorption rate is low, anti-folding, it is freeze proof, acidproof, alkaline-resisting, will never fade, Equal remarkable advantages.Workshop, the industry such as house, hotel, villa and civil buildings are widely used in, and with its various shapes, glaze colours It is simple, colorful, it is environmentally friendly, durable, firmly get the high praise of building great masters.
Currently, glaze sintering temperature is often higher than 1000 DEG C.As CN201510295161.2 disclose it is a kind of it is acidproof it is resistance to freeze it is red The preparation method of mud glazed tiles, with 50-80 parts of red mud;10-20 parts of talcum;4-5 parts of quartz sand;4-5 parts of albite;Tripolyphosphate 1-3 parts of sodium;1-3 parts of cellulose;1-3 parts of silicon carbide are raw material, take and strengthen to the green body after glazing using two-step sintering, twice Method, the glazed tiles of low water absorption strong with acidproof resistance to its anti-pressure ability of jelly are prepared;Its simple process is conducive to industry Change, but its sintering temperature is 1450 degrees Celsius, belongs to highly energy-consuming;Such as Zou little Ling, in " Chinese pottery " the 06th phase in 2016 Using Pb-Zn-Ag ore tailing as primary raw material, it is aided with red soil, kaolin, forms compact structure coloured glaze in 1160~1170 DEG C of calcinings Watt.The result shows that: use formula composition for Pb-Zn-Ag ore tailing 36~37%, 45~46% kaolin 18~19% of red soil, system The glazed tiles green body obtained, XRD analysis principal crystalline phase have quartz, anorthite, mullite etc., and scanning electron microscope (SEM) is the result shows that coloured glaze Unbaked tile body particle close-packed arrays have a small amount of gap between particle.Glaze is more smooth, and glaze-ceramic interface is close.The water suction of sample The indexs such as rate, bending failure loading, thermal stability and frost resistance can reach " colored glaze product " JC/T765-2006 mark Alignment request.Pb-Zn tailings are not only utilized in this, alleviate its pollution to environment, and reduce glazed tiles production cost, change give up into It is precious.But its sintering temperature is 1160~1170 DEG C, belongs to highly energy-consuming, pollutes environment, therefore, following development is inevitable toward low temperature Sintering, energy conservation and environmental protection development.The reduction of sintering temperature can reduce energy consumption, meet the needs of social development.Ultralow sintering process Research, keeps its purposes more extensive, can be used in the reparation of glazed tiles product defect, reduce the substandard products of coloured glaze watt of goods, reduce The waste of resource, but existing glazed tiles are formed using a variety of pug mixed sinterings, it is more traditional with material, cause Existing glazed tiles plasticity is bad, and cracking will be easy after stress and is crushed, service life is short.Its glaze layer is generally thicker and generates and answers Power, quality weight easily lead to the defect that product glaze cracking occurs, collapses stripping.It is not smooth enough, and pug is easy in process of production Pollution is generated, the quality of product is not sufficiently stable, and glaze glossiness is inadequate, and colour generation is not abundant enough, stablizes, in climate variability area Or sintering temperature height when colour fading and sintering glazed tiles additive therefor application at present is easy under prolonged sunlight irradiation, Firing time is long, and structural compactness is low, to be unable to extensive utilization, therefore is badly in need of researching and developing a kind of novel glazed tiles addition used Agent meets the needs of people.
Summary of the invention
The technical problems to be solved by the invention: sintering temperature when for current sintering glazed tiles additive therefor application Height, firing time is long, the low problem of structural compactness, provides a kind of low temperature burning glazed tiles additive.
In order to solve the above technical problems, the present invention is using technical solution as described below:
A kind of low temperature burns glazed tiles additive, according to parts by weight, including following component: 4 ~ 8 parts of quartz sands, 2 ~ 4 parts of waterglass, 1 ~ 4 part of auxiliary material, 3 ~ 6 portions of reinforcing agents, 15 ~ 25 parts of compound action base-materials, 10 ~ 14 parts of composite fillers.
The preparation method of the compound action base-material, includes the following steps:
(1) take pug 15 ~ 25:3:2 in mass ratio be added magnetic iron ore, blast furnace titaniferous slag mixed grinding, obtain abrasive, take abrasive by Mass ratio 3:8 ~ 14 is added sulfuric acid solution and is mixed, and filtering takes filter residue and drying, obtains dried object, in 55 ~ 70 DEG C, takes dried object 1:6 in mass ratio ~ 10 is added ammonia spirit and is mixed, centrifugation, and collection centrifugation object is dry, calcines, cooling, must calcine material, take Calcining material pulverizes and sieves, and collects sieving particle, obtains combined processing object;
(2) according to parts by weight, 20 ~ 35 parts of combined processing objects, 3 ~ 7 parts of perlites, 2 ~ 5 parts of butyl stearates, 2 ~ 5 parts of crosslinkings are taken Agent, 50 ~ 70 parts of water take perlite, butyl stearate, crosslinking agent, water to be mixed, are warming up to 60 ~ 75 DEG C prior to 30 ~ 50 DEG C, Combined processing object is added to be mixed, rotary evaporation, Freezing smashing sieving, collects sieving particle to get compound action base-material.
Pug in the step (1): 2 ~ 5:1:1 in mass ratio takes boron mud, red mud, metakaolin mixing to get pug.
Crosslinking agent in the step (2): in 30 ~ 46 DEG C, 6 ~ 10:0.3:35 ~ 45 in mass ratio take hexa-methylene two different Cyanate, silane resin acceptor kh-550, tetrahydrofuran mixing, lead to argon gas protection, and stirring obtains mixed liquor, takes mixed liquor by quality Hexamethylene diisocyanate, sodium citrate mixing is added than 12 ~ 16:1 ~ 3:1, rotary evaporation is to get crosslinking agent.
The preparation of the composite filler: matrix fillers 1:10 ~ 15 in mass ratio plus water mixing are taken, in 30 ~ 50 DEG C of ultrasounds Processing, obtains dispersion liquid, takes dispersion liquid 12 ~ 18:5 in mass ratio that carbon nanotube is added in 6 ~ 10 DEG C and is mixed, filtering must filter Slag, in 22 ~ 27 DEG C, 8 ~ 12:3:28 in mass ratio takes filter residue, ceria, reagent mixing, leads to nitrogen protection, is warming up to 45 ~ 65 DEG C, the inducing agent mixing of filter residue quality 6 ~ 10% is added, insulated and stirred is evaporated under reduced pressure, obtains concentrate, concentrate is taken to wash, does It is dry to get composite filler.
Described matrix filler: 1:2 ~ 5:0.2 in mass ratio takes white carbon black, graphene, microcrystalline cellulose mixing to get matrix Filler.
The reagent: 8 ~ 13:5 in mass ratio takes hydrochloric acid solution, hydrogen peroxide mixing to get reagent.
The inducing agent: 3 ~ 7:1 in mass ratio takes pyridine -2,6- dioctyl phthalate, sodium peroxydisulfate mixing to get inducing agent.
The auxiliary material: 1:1:2 ~ 4 take nano zine oxide, barium carbonate, aluminum phosphate mixing to get auxiliary material in mass ratio.
The reinforcing agent: 2 ~ 4:1:1 in mass ratio takes polyvinyl alcohol, titanium dioxide, calcium bicarbonate mixing to get reinforcing agent.
The present invention is compared with other methods, and advantageous effects are:
(1) present invention is activated using pug and magnetic iron ore, blast furnace titaniferous slag grinding, adds sulfuric acid solution, removes deacidification melt into point, right Layer chain structure contained by pug is destroyed, its specific surface area is improved, and absorption is convenient for molecule, improves interstructural densification Property, the isocyanate prepolymer composition contained in made crosslinker component can be combined into silane coupling agent ingredient with bridge crosslinking structure Siloxanes provides hybrid inorganic-organic synergistic effect, facilitates the compactness inside being promoted, the Nano grade that the present invention adds Raw material-nano zine oxide and calcium bicarbonate be thermally generated it is small it is calcium carbonate-filled wherein, ruler can be played in mixed process Very little effect and quantum effect achieve the effect that melting as early as possible, favorably so that the fusing point of blended material reduces during the sintering process In reducing sintering temperature, shorten sintering time;
(2) present invention is ultrasonically treated the matrix fillers containing white carbon black, graphene, microcrystalline cellulose, with cavitation effect Suction function promotes its dispersion effect, and is blended with the carbon nanotube of addition, in the process, plays prior to 6 ~ 10 DEG C The hydrophily that carbon nano tube network has can be such that matrix fillers are attracted in the net hole of carbon nano tube network, then be warming up to 22 ~ 27 DEG C, the hydrophily for changing carbon nanotube is hydrophobicity, and hydrone is driven away, and leaves matrix fillers absorption and is filled in carbon It in the net hole of nanotube reticular membrane, provides small and has more activation sites, improve the inside interaction of this additive system, mention Inside solid degree is risen, in addition, cerium oxide is handled with oxidation acid solution reagent, obtains part Ce3+、Ce4+, and with pyridine -2,6- Dioctyl phthalate is chelated, sodium peroxydisulfate further aoxidizes, and improves the stability of the compound containing Ce, can also play the work of storage oxygen With, and at relatively high temperatures, pyridine -2,6- dioctyl phthalate thermal dehydration generates carbon dioxide, it can also assist getting through hole, so that Made glazed tiles internal combustion more closely, to improve its compactness and plasticity, while ceria can also release Oxygen improves thermal effect, reduces firing time, promotes to remain carbonaceous component oxygenolysis, during further strengthening glazed tiles processed Internal consistency improves the consistency of be sintered glazed tiles;
(3) present invention handles pug, siliceous ingredient, is cooperateed with, and fill molecule, is mentioned by hybrid inorganic-organic The consistency after being sintered inside glazed tiles is risen, and uses carbon nano-tube network network diagram collection activity hard constituents, in conjunction with the storage of metallic cerium Oxygen and aiding combustion effect, promotes fuel efficiency, reduces firing time, improves consistency, the present invention is for sintering glazed tiles addition used at present Sintering temperature when agent is applied is high, and firing time is long, and the low problem of structural compactness, improvement is significant, has and answers well Use prospect.
Specific embodiment
Pug: 2 ~ 5:1:1 in mass ratio takes boron mud, red mud, metakaolin mixing to get pug.
Auxiliary material: 1:1:2 ~ 4 take nano zine oxide, barium carbonate, aluminum phosphate mixing to get auxiliary material in mass ratio.
Reinforcing agent: 2 ~ 4:1:1 in mass ratio takes polyvinyl alcohol, titanium dioxide, calcium bicarbonate mixing to get reinforcing agent.
Crosslinking agent: in 30 ~ 46 DEG C, 6 ~ 10:0.3:35 ~ 45 take hexamethylene diisocyanate, silane coupled in mass ratio Agent KH-550, tetrahydrofuran are mixed in reaction kettle, are led to argon gas protection, with 600 ~ 900r/min, 40 ~ 60min of magnetic agitation, are obtained mixed Liquid is closed, takes mixed liquor 12 ~ 16:1 in mass ratio ~ 3:1 that hexamethylene diisocyanate, sodium citrate 1 ~ 3h of mixing is added, Rotary evaporation is to constant weight to get crosslinking agent.
Matrix fillers: 1:2 ~ 5:0.2 in mass ratio takes white carbon black, graphene, microcrystalline cellulose mixing to fill out to get matrix Material.
Reagent: 8 ~ 13:5 in mass ratio takes the hydrochloric acid solution that mass fraction is 12%, the hydrogen peroxide of concentration 0.5mol/L mixed It closes to get reagent.
Inducing agent: 3 ~ 7:1 in mass ratio takes pyridine -2,6- dioctyl phthalate, sodium peroxydisulfate mixing to get inducing agent.
The preparation method of compound action base-material, includes the following steps:
(1) it takes pug 15 ~ 25:3:2 in mass ratio that magnetic iron ore, blast furnace titaniferous slag is added in mortar mixing, is ground with 350 ~ 550r/min Grind 2 ~ 4h, obtain abrasive, take abrasive 3:8 in mass ratio ~ 14 be added mass fraction be 15% sulfuric acid solution be mixed 25 ~ 50min, filtering, takes filter residue in 90 ~ 100 DEG C of 1 ~ 3h of oven drying, obtains dried object, in 55 ~ 70 DEG C, take dried object in mass ratio 1: 6 ~ 10 be added mass fractions be 18% ammonia spirit be mixed 30 ~ 50min, move to centrifuge with 3000 ~ 5000r/min from 10 ~ 15min of the heart collects centrifugation object after 70 ~ 85 DEG C of 4 ~ 8h of oven drying, moves to Muffle furnace, with 300 ~ 550 DEG C of 2 ~ 4h of calcining, It cools to room temperature with the furnace, material must be calcined, calcining material is taken to sieve with 100 mesh sieve in pulverizer crushing, collect sieving particle, obtain combined processing Object;
(2) according to parts by weight, 20 ~ 35 parts of combined processing objects, 3 ~ 7 parts of perlites, 2 ~ 5 parts of butyl stearates, 2 ~ 5 parts of crosslinkings are taken Agent, 50 ~ 70 parts of water take perlite, butyl stearate, crosslinking agent, water to mix in reaction kettle prior to 30 ~ 50 DEG C, with 500 ~ 800r/min 35 ~ 60min of magnetic agitation is warming up to 60 ~ 75 DEG C, combined processing object is added, 1 ~ 3h is mixed, rotary evaporation is extremely Constant weight moves to freezing crusher, crushed 120 meshes, collects sieving particle to get compound action base-material.
The preparation of composite filler: take matrix fillers 1:10 in mass ratio ~ 15 that ultrapure water is added mixed in ultrasonic oscillation instrument Close, in 30 ~ 50 DEG C, with 50 ~ 65kHz frequency ultrasound handle 1 ~ 3h, obtain dispersion liquid, taken in 6 ~ 10 DEG C dispersion liquid in mass ratio 12 ~ Carbon nanotube mixing is added in 18:5, and with 2000 ~ 4000r/min, 40 ~ 60min of magnetic agitation, filtering obtains filter residue, in 22 ~ 27 DEG C, 8 ~ 12:3:28 in mass ratio takes filter residue, ceria, reagent to stir 30 ~ 55min in reaction kettle, leads to nitrogen protection, is warming up to 45 ~ 65 DEG C, the inducing agent mixing of filter residue quality 6 ~ 10% is added, 40 ~ 60min of insulated and stirred is evaporated under reduced pressure to constant weight, obtains concentrate, After taking concentrate to be washed with water 3 ~ 5 times, 60 ~ 80 DEG C of 4 ~ 8h of oven drying are moved to get composite filler.
A kind of low temperature burning glazed tiles additive, according to parts by weight, including following component: 4 ~ 8 parts of quartz sands, 2 ~ 4 parts of water Glass, 1 ~ 4 part of auxiliary material, 3 ~ 6 portions of reinforcing agents, 15 ~ 25 parts of compound action base-materials, 10 ~ 14 parts of composite fillers.
Pug: 2:1:1 in mass ratio takes boron mud, red mud, metakaolin mixing to get pug.
Auxiliary material: 1:1:2 in mass ratio takes nano zine oxide, barium carbonate, aluminum phosphate mixing to get auxiliary material.
Reinforcing agent: 2:1:1 in mass ratio takes polyvinyl alcohol, titanium dioxide, calcium bicarbonate mixing to get reinforcing agent.
Crosslinking agent: in 30 DEG C, 6:0.3:35 in mass ratio take hexamethylene diisocyanate, silane resin acceptor kh-550, Tetrahydrofuran is mixed in reaction kettle, is led to argon gas protection, with 600r/min magnetic agitation 40min, is obtained mixed liquor, take mixed liquor by matter Hexamethylene diisocyanate is added than 12:1:1 in amount, 1h is mixed in sodium citrate, and rotary evaporation to constant weight is to get crosslinking Agent.
Matrix fillers: 1:2:0.2 in mass ratio takes white carbon black, graphene, microcrystalline cellulose mixing to get matrix fillers.
Reagent: 8:5 in mass ratio takes the hydrochloric acid solution that mass fraction is 12%, the hydrogen peroxide mixing of concentration 0.5mol/L, i.e., Obtain reagent.
Inducing agent: 3:1 in mass ratio takes pyridine -2,6- dioctyl phthalate, sodium peroxydisulfate mixing to get inducing agent.
The preparation method of compound action base-material, includes the following steps:
(1) it takes pug 15:3:2 in mass ratio that magnetic iron ore, blast furnace titaniferous slag is added in mortar mixing, 2h is ground with 350r/min, is obtained Abrasive takes abrasive 3:8 in mass ratio that the sulfuric acid solution that mass fraction is 15% is added and 25min is mixed, and filtering takes filter Slag obtains dried object in 90 DEG C of oven drying 1h, in 55 DEG C, takes dried object 1:6 in mass ratio that the ammonium hydroxide that mass fraction is 18% is added 30min is mixed in solution, moves to centrifuge with 3000r/min and is centrifuged 10min, collects centrifugation object in 70 DEG C of oven drying 4h Afterwards, Muffle furnace is moved to, with 300 DEG C of calcining 2h, room temperature is cooled to the furnace, material must be calcined, calcining material is taken to crushed 100 in pulverizer Mesh collects sieving particle, obtains combined processing object;
(2) according to parts by weight, 20 parts of combined processing objects, 3 parts of perlites, 2 parts of butyl stearates, 2 parts of crosslinking agents, 50 parts are taken Water takes perlite, butyl stearate, crosslinking agent, water to mix in reaction kettle, prior to 30 DEG C with 500r/min magnetic agitation 35min is warming up to 60 DEG C, combined processing object is added, 1h is mixed, and rotary evaporation to constant weight moves to freezing crusher, crushes 120 meshes are crossed, collect sieving particle to get compound action base-material.
The preparation of composite filler: taking matrix fillers 1:10 in mass ratio that ultrapure water is added and mix in ultrasonic oscillation instrument, In 30 DEG C, 1h is handled with 50kHz frequency ultrasound, obtains dispersion liquid, takes dispersion liquid 12:5 in mass ratio that carbon nanotube is added in 6 DEG C mixed Close, with 2000r/min magnetic agitation 40min, filtering obtains filter residue, in 22 DEG C, 8:3:28 in mass ratio take filter residue, ceria, Reagent stirs 30min in reaction kettle, leads to nitrogen protection, is warming up to 45 DEG C, and the inducing agent mixing of filter residue quality 6% is added, and heat preservation is stirred Mix 40min, be evaporated under reduced pressure to constant weight, obtain concentrate, after taking concentrate to be washed with water 3 times, move to 60 DEG C of oven drying 4h to get Composite filler.
A kind of low temperature burns glazed tiles additive, according to parts by weight, including following component: 4 parts of quartz sands, 2 parts of waterglass, 1 part of auxiliary material, 3 portions of reinforcing agents, 15 parts of compound action base-materials, 10 parts of composite fillers.
Pug: 5:1:1 in mass ratio takes boron mud, red mud, metakaolin mixing to get pug.
Auxiliary material: 1:1:4 in mass ratio takes nano zine oxide, barium carbonate, aluminum phosphate mixing to get auxiliary material.
Reinforcing agent: 4:1:1 in mass ratio takes polyvinyl alcohol, titanium dioxide, calcium bicarbonate mixing to get reinforcing agent.
Crosslinking agent: in 46 DEG C, 10:0.3:45 in mass ratio take hexamethylene diisocyanate, silane resin acceptor kh-550, Tetrahydrofuran is mixed in reaction kettle, is led to argon gas protection, with 900r/min magnetic agitation 60min, is obtained mixed liquor, take mixed liquor by matter Hexamethylene diisocyanate is added than 16:3:1 in amount, 3h is mixed in sodium citrate, and rotary evaporation to constant weight is to get crosslinking Agent.
Matrix fillers: 1:5:0.2 in mass ratio takes white carbon black, graphene, microcrystalline cellulose mixing to get matrix fillers.
Reagent: 13:5 in mass ratio takes the hydrochloric acid solution that mass fraction is 12%, the hydrogen peroxide mixing of concentration 0.5mol/L, Up to reagent.
Inducing agent: 7:1 in mass ratio takes pyridine -2,6- dioctyl phthalate, sodium peroxydisulfate mixing to get inducing agent.
The preparation method of compound action base-material, includes the following steps:
(1) it takes pug 25:3:2 in mass ratio that magnetic iron ore, blast furnace titaniferous slag is added in mortar mixing, 4h is ground with 550r/min, is obtained Abrasive takes abrasive 3:14 in mass ratio that the sulfuric acid solution that mass fraction is 15% is added and 50min is mixed, and filtering takes filter Slag obtains dried object in 100 DEG C of oven drying 3h, in 70 DEG C, takes dried object 1:10 in mass ratio that the ammonia that mass fraction is 18% is added 50min is mixed in aqueous solution, moves to centrifuge with 5000r/min and is centrifuged 15min, collects centrifugation object in 85 DEG C of oven drying 8h Afterwards, Muffle furnace is moved to, with 550 DEG C of calcining 4h, room temperature is cooled to the furnace, material must be calcined, calcining material is taken to crushed 100 in pulverizer Mesh collects sieving particle, obtains combined processing object;
(2) according to parts by weight, 35 parts of combined processing objects, 7 parts of perlites, 5 parts of butyl stearates, 5 parts of crosslinking agents, 70 parts are taken Water takes perlite, butyl stearate, crosslinking agent, water to mix in reaction kettle, prior to 50 DEG C with 800r/min magnetic agitation 60min is warming up to 75 DEG C, combined processing object is added, 3h is mixed, and rotary evaporation to constant weight moves to freezing crusher, crushes 120 meshes are crossed, collect sieving particle to get compound action base-material.
The preparation of composite filler: taking matrix fillers 1:15 in mass ratio that ultrapure water is added and mix in ultrasonic oscillation instrument, In 50 DEG C, 3h is handled with 65kHz frequency ultrasound, obtains dispersion liquid, takes dispersion liquid 18:5 in mass ratio that carbon nanotube is added in 10 DEG C Mixing, with 4000r/min magnetic agitation 60min, filtering obtains filter residue, in 27 DEG C, 12:3:28 in mass ratio takes filter residue, titanium dioxide Cerium, reagent stir 55min in reaction kettle, lead to nitrogen protection, are warming up to 65 DEG C, and the inducing agent mixing of filter residue quality 10% is added, protects Temperature stirring 60min, is evaporated under reduced pressure to constant weight, obtains concentrate, after taking concentrate to be washed with water 5 times, move to 80 DEG C of oven drying 8h, Up to composite filler.
A kind of low temperature burns glazed tiles additive, according to parts by weight, including following component: 8 parts of quartz sands, 4 parts of waterglass, 4 parts of auxiliary materials, 6 portions of reinforcing agents, 25 parts of compound action base-materials, 14 parts of composite fillers.
Pug: 3:1:1 in mass ratio takes boron mud, red mud, metakaolin mixing to get pug.
Auxiliary material: 1:1:3 in mass ratio takes nano zine oxide, barium carbonate, aluminum phosphate mixing to get auxiliary material.
Reinforcing agent: 3:1:1 in mass ratio takes polyvinyl alcohol, titanium dioxide, calcium bicarbonate mixing to get reinforcing agent.
Crosslinking agent: in 36 DEG C, 8:0.3:40 in mass ratio take hexamethylene diisocyanate, silane resin acceptor kh-550, Tetrahydrofuran is mixed in reaction kettle, is led to argon gas protection, with 800r/min magnetic agitation 50min, is obtained mixed liquor, take mixed liquor by matter Hexamethylene diisocyanate is added than 15:2:1 in amount, 2h is mixed in sodium citrate, and rotary evaporation to constant weight is to get crosslinking Agent.
Matrix fillers: 1:3:0.2 in mass ratio takes white carbon black, graphene, microcrystalline cellulose mixing to get matrix fillers.
Reagent: 11:5 in mass ratio takes the hydrochloric acid solution that mass fraction is 12%, the hydrogen peroxide mixing of concentration 0.5mol/L, Up to reagent.
Inducing agent: 5:1 in mass ratio takes pyridine -2,6- dioctyl phthalate, sodium peroxydisulfate mixing to get inducing agent.
The preparation method of compound action base-material, includes the following steps:
(1) it takes pug 20:3:2 in mass ratio that magnetic iron ore, blast furnace titaniferous slag is added in mortar mixing, 3h is ground with 450r/min, is obtained Abrasive takes abrasive 3:12 in mass ratio that the sulfuric acid solution that mass fraction is 15% is added and 40min is mixed, and filtering takes filter Slag obtains dried object in 95 DEG C of oven drying 2h, in 60 DEG C, takes dried object 1:8 in mass ratio that the ammonium hydroxide that mass fraction is 18% is added 40min is mixed in solution, moves to centrifuge with 4000r/min and is centrifuged 12min, collects centrifugation object in 75 DEG C of oven drying 6h Afterwards, Muffle furnace is moved to, with 450 DEG C of calcining 3h, room temperature is cooled to the furnace, material must be calcined, calcining material is taken to crushed 100 in pulverizer Mesh collects sieving particle, obtains combined processing object;
(2) according to parts by weight, 25 parts of combined processing objects, 5 parts of perlites, 3 parts of butyl stearates, 3 parts of crosslinking agents, 60 parts are taken Water takes perlite, butyl stearate, crosslinking agent, water to mix in reaction kettle, prior to 40 DEG C with 700r/min magnetic agitation 50min is warming up to 65 DEG C, combined processing object is added, 2h is mixed, and rotary evaporation to constant weight moves to freezing crusher, crushes 120 meshes are crossed, collect sieving particle to get compound action base-material.
The preparation of composite filler: taking matrix fillers 1:12 in mass ratio that ultrapure water is added and mix in ultrasonic oscillation instrument, In 40 DEG C, 2h is handled with 55kHz frequency ultrasound, obtains dispersion liquid, takes dispersion liquid 15:5 in mass ratio that carbon nanotube is added in 8 DEG C mixed It closes, with 3000r/min magnetic agitation 50min, filtering obtains filter residue, in 25 DEG C, 10:3:28 in mass ratio takes filter residue, titanium dioxide Cerium, reagent stir 45min in reaction kettle, lead to nitrogen protection, are warming up to 55 DEG C, and the inducing agent mixing of filter residue quality 8% is added, protects Temperature stirring 50min, is evaporated under reduced pressure to constant weight, obtains concentrate, after taking concentrate to be washed with water 4 times, move to 70 DEG C of oven drying 6h, Up to composite filler.
A kind of low temperature burns glazed tiles additive, according to parts by weight, including following component: 6 parts of quartz sands, 3 parts of waterglass, 2 parts of auxiliary materials, 5 portions of reinforcing agents, 20 parts of compound action base-materials, 12 parts of composite fillers.
Comparative example 1: it is essentially identical with the preparation method of embodiment 1, it has only the difference is that lacking compound action base-material.
Comparative example 2: it is essentially identical with the preparation method of embodiment 1, it has only the difference is that lacking composite filler.
Comparative example 3: the low-temperature sintering glazed tiles additive of company, Hebei province production.
The low temperature that above-described embodiment is obtained with comparative example is burnt glazed tiles additive to detect, bending strength: using curved Bent strength-testing machine is measured;Other are detected using " colored glaze product " JC/T765-2006 standard, obtained knot Fruit is as shown in table 1.
Table 1:
In summary, to burn glazed tiles additive effect more preferable for low temperature of the invention as can be seen from Table 1, is worth of widely use, with The upper preferred mode only of the invention, is not intended to limit the invention, all within the spirits and principles of the present invention, is made Any modification, equivalent substitution, improvement and etc., should all be included in the protection scope of the present invention.

Claims (10)

1. a kind of low temperature burns glazed tiles additive, according to parts by weight, including following component: 4 ~ 8 parts of quartz sands, 2 ~ 4 parts of water glass Glass, 1 ~ 4 part of auxiliary material, 3 ~ 6 portions of reinforcing agents, which is characterized in that further include: 15 ~ 25 parts of compound action base-materials, 10 ~ 14 parts compound fill out Charge.
2. a kind of low temperature burns glazed tiles additive according to claim 1, which is characterized in that the system of the compound action base-material Preparation Method includes the following steps:
(1) take pug 15 ~ 25:3:2 in mass ratio be added magnetic iron ore, blast furnace titaniferous slag mixed grinding, obtain abrasive, take abrasive by Mass ratio 3:8 ~ 14 is added sulfuric acid solution and is mixed, and filtering takes filter residue and drying, obtains dried object, in 55 ~ 70 DEG C, takes dried object 1:6 in mass ratio ~ 10 is added ammonia spirit and is mixed, centrifugation, and collection centrifugation object is dry, calcines, cooling, must calcine material, take Calcining material pulverizes and sieves, and collects sieving particle, obtains combined processing object;
(2) according to parts by weight, 20 ~ 35 parts of combined processing objects, 3 ~ 7 parts of perlites, 2 ~ 5 parts of butyl stearates, 2 ~ 5 parts of crosslinkings are taken Agent, 50 ~ 70 parts of water take perlite, butyl stearate, crosslinking agent, water to be mixed, are warming up to 60 ~ 75 DEG C prior to 30 ~ 50 DEG C, Combined processing object is added to be mixed, rotary evaporation, Freezing smashing sieving, collects sieving particle to get compound action base-material.
3. a kind of low temperature burns glazed tiles additive according to claim 2, which is characterized in that the pug in the step (1): 2 ~ 5:1:1 in mass ratio takes boron mud, red mud, metakaolin mixing to get pug.
4. a kind of low temperature burns glazed tiles additive according to claim 2, which is characterized in that the crosslinking in the step (2) Agent: in 30 ~ 46 DEG C, 6 ~ 10:0.3:35 ~ 45 in mass ratio take hexamethylene diisocyanate, silane resin acceptor kh-550, tetrahydro Argon gas protection is led in furans mixing, and stirring obtains mixed liquor, takes mixed liquor 12 ~ 16:1 in mass ratio ~ 3:1 that hexa-methylene two is added different Cyanate, sodium citrate are mixed, and rotary evaporation is to get crosslinking agent.
5. a kind of low temperature burns glazed tiles additive according to claim 1, which is characterized in that the system of the composite filler It is standby: to take matrix fillers 1:10 ~ 15 in mass ratio plus water mixing, be ultrasonically treated in 30 ~ 50 DEG C, obtain dispersion liquid, taken in 6 ~ 10 DEG C point Dispersion liquid 12 ~ 18:5 in mass ratio is added carbon nanotube and is mixed, and filtering obtains filter residue, in 22 ~ 27 DEG C, in mass ratio 8 ~ 12:3: 28 take filter residue, ceria, reagent mixing, lead to nitrogen protection, are warming up to 45 ~ 65 DEG C, the inducing agent of filter residue quality 6 ~ 10% is added Mixing, insulated and stirred are evaporated under reduced pressure, obtain concentrate, concentrate is taken to wash, dry to get composite filler.
6. a kind of low temperature burns glazed tiles additive according to claim 5, which is characterized in that described matrix filler: pressing quality Take white carbon black, graphene, microcrystalline cellulose mixing to get matrix fillers than 1:2 ~ 5:0.2.
7. a kind of low temperature burns glazed tiles additive according to claim 5, which is characterized in that the reagent: in mass ratio 8 ~ 13:5 takes hydrochloric acid solution, hydrogen peroxide mixing to get reagent.
8. a kind of low temperature burns glazed tiles additive according to claim 5, which is characterized in that the inducing agent: in mass ratio 3 ~ 7:1 takes pyridine -2,6- dioctyl phthalate, sodium peroxydisulfate mixing to get inducing agent.
9. a kind of low temperature burns glazed tiles additive according to claim 1, which is characterized in that the auxiliary material: in mass ratio 1: 1:2 ~ 4 take nano zine oxide, barium carbonate, aluminum phosphate mixing to get auxiliary material.
10. a kind of low temperature burns glazed tiles additive according to claim 1, which is characterized in that the reinforcing agent: in mass ratio 2 ~ 4:1:1 takes polyvinyl alcohol, titanium dioxide, calcium bicarbonate mixing to get reinforcing agent.
CN201910326018.3A 2019-04-23 2019-04-23 A kind of low temperature burning glazed tiles additive Pending CN110015902A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910326018.3A CN110015902A (en) 2019-04-23 2019-04-23 A kind of low temperature burning glazed tiles additive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910326018.3A CN110015902A (en) 2019-04-23 2019-04-23 A kind of low temperature burning glazed tiles additive

Publications (1)

Publication Number Publication Date
CN110015902A true CN110015902A (en) 2019-07-16

Family

ID=67192161

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910326018.3A Pending CN110015902A (en) 2019-04-23 2019-04-23 A kind of low temperature burning glazed tiles additive

Country Status (1)

Country Link
CN (1) CN110015902A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114671610A (en) * 2019-08-26 2022-06-28 福建省德化县天俊陶瓷有限公司 Low-temperature transparent glazed ceramic product and preparation method thereof
CN117735868A (en) * 2024-02-21 2024-03-22 北京安科兴业科技股份有限公司 Method for preparing magnesium silicate cementing material by taking solid waste boron mud as raw material

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101857261A (en) * 2010-06-29 2010-10-13 上海大学 Method for preparing nano Ce(OH)3 powder
CN106082958A (en) * 2016-06-22 2016-11-09 徐晓 A kind of preparation method of low grade fever's glazed tiles additive
CN108726567A (en) * 2018-08-13 2018-11-02 合肥汉甲陶瓷科技有限公司 A kind of nano zirconia material that environment-friendly high-intensity easily disperses

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101857261A (en) * 2010-06-29 2010-10-13 上海大学 Method for preparing nano Ce(OH)3 powder
CN106082958A (en) * 2016-06-22 2016-11-09 徐晓 A kind of preparation method of low grade fever's glazed tiles additive
CN108726567A (en) * 2018-08-13 2018-11-02 合肥汉甲陶瓷科技有限公司 A kind of nano zirconia material that environment-friendly high-intensity easily disperses

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
宁桂玲: "《高等无机合成》", 30 September 2007 *
李新梅: "高比表面积煤系高岭土材料的制备及其结构表征", 《石河子大学学报(自然科学版)》 *
石富: "《稀土冶金技术》", 30 April 2009 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114671610A (en) * 2019-08-26 2022-06-28 福建省德化县天俊陶瓷有限公司 Low-temperature transparent glazed ceramic product and preparation method thereof
CN114671610B (en) * 2019-08-26 2023-05-23 福建省德化县天俊陶瓷有限公司 Low-temperature transparent glaze ceramic product and preparation method thereof
CN117735868A (en) * 2024-02-21 2024-03-22 北京安科兴业科技股份有限公司 Method for preparing magnesium silicate cementing material by taking solid waste boron mud as raw material
CN117735868B (en) * 2024-02-21 2024-04-30 北京安科兴业科技股份有限公司 Method for preparing magnesium silicate cementing material by taking solid waste boron mud as raw material

Similar Documents

Publication Publication Date Title
WO2019141098A1 (en) High-value comprehensive utilization method for lithium slag
CN100453498C (en) Ultra-thin ceramic outside-wall brick and production method thereof
CN109851376B (en) Tin bath bottom brick, preparation method thereof and composition for preparing tin bath bottom brick
CN106746817B (en) A kind of microwave sintering method of granite stone powder haydite
CN110028303B (en) Reinforced porcelain prepared from common domestic ceramic blank and preparation method thereof
CN100343195C (en) Low temperature semi-porcelain and its preparation method
CN103288426A (en) Method for preparing special fracturing propping agent for shale gas by utilizing industrial waste
CN104371703B (en) A kind of method that petroleum fracturing propping agent is prepared by raw material of aluminous fly-ash
CN108046650A (en) A kind of cement synergist
CN110015902A (en) A kind of low temperature burning glazed tiles additive
CN109776067A (en) A method of sintering seepy material is prepared using clay
CN110002848A (en) A kind of wear-resisting high-ductility material of 3D printing ceramics
CN105924223A (en) Electrolytic manganese residue fired perforated brick and preparation method thereof
CN1919765A (en) Glass-ceramic plate produced from waste glass
CN108975950A (en) A kind of refractory brick of high temperature resistance and high strength and preparation method thereof
CN114702298B (en) Deep color whole-body landscape thick brick and preparation method thereof
CN110317016A (en) A kind of water proof anti-seepage aerated bricks
CN104496433B (en) It is a kind of using Tungsten tailing as high-strength ceramic of primary raw material and preparation method thereof
CN112125644A (en) Sanitary ceramic and preparation method thereof
CN108516795A (en) A kind of lightening fire resistant ceramic and preparation method thereof
CN105948505A (en) Preparation method for lead-zinc-silver tailing low-temperature-sintered encaustic brick glaze
CN109095904A (en) A kind of low temperature fast firing Dali stone ceramic tile and preparation method thereof
CN105036167A (en) Calcium hexaluminate and preparation method thereof
CN107879752A (en) A kind of preparation method of the low apparent porosity honeycomb ceramic heat accumulator of high temperature resistant
CN116947352A (en) Method for medium-temperature thermal activation of coal gangue

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