CN108689604A - The preparation method of far infrared ceramic tile - Google Patents
The preparation method of far infrared ceramic tile Download PDFInfo
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- CN108689604A CN108689604A CN201810704539.3A CN201810704539A CN108689604A CN 108689604 A CN108689604 A CN 108689604A CN 201810704539 A CN201810704539 A CN 201810704539A CN 108689604 A CN108689604 A CN 108689604A
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- far infrared
- coat enamel
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- overglaze
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C8/00—Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/009—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
- C04B41/52—Multiple coating or impregnating multiple coating or impregnating with the same composition or with compositions only differing in the concentration of the constituents, is classified as single coating or impregnation
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/80—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only ceramics
- C04B41/81—Coating or impregnation
- C04B41/89—Coating or impregnation for obtaining at least two superposed coatings having different compositions
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Structural Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Finishing Walls (AREA)
- Paints Or Removers (AREA)
Abstract
The present invention discloses a kind of preparation method of far infrared ceramic tile, includes the following steps:Blank forming, it is dry;Billet surface after the drying applies far infrared ground-coat enamel, dry;Far infrared overglaze is applied on far infrared ground-coat enamel surface after the drying, dry;It fires, obtains semi-finished product;Semi-finished product are polished, edging, obtain finished product;Super clean bright processing is carried out to get far infrared ceramic tile to finished surface;The component of the far infrared ground-coat enamel includes aluminium oxide, silica, calcium oxide, potassium oxide, magnesia, barium monoxide, far infrared additive, styrene and trisiloxanes ethylene glycol;The component of the far infrared overglaze includes aluminium oxide, silica, calcium oxide, potassium oxide, magnesia, barium monoxide, sodium oxide molybdena, far infrared additive, styrene and trisiloxanes ethylene glycol.Technical scheme of the present invention enables to ceramic tile to have far infrared emission function.
Description
Technical field
The present invention relates to ceramic tile technical field, more particularly to a kind of preparation method of far infrared ceramic tile.
Background technology
In recent years, with the continuous deterioration of ecological environment and stepping up for people's living standard, public space and household
The construction of health environment in space becomes the topic of people's close attention.
Far infrared can effectively be absorbed as a kind of electromagnetic wave by human body.Deeply far infrared into the human body
Line can cause the vibration of atom and molecule, and by resonant absorption, form thermal response and promote in subcutaneous deep tissues temperature
It rises, fine vascular expansion;To promote blood circulation, the obstacle cleaning that extravasated blood etc. is harmed to metabolism is clean, and tissue is made to obtain
To bring back to life, and ferment is promoted to grow, so that it is trapped in old waste and the harmful substance in human body originally, it can be with new
Old metabolism is excreted by sweat gland.Concurrently there are the residue of such as cosmetics in pore, also can directly by pore with
Sweat excretes together, effectively to mitigate the burden of kidney.
Currently, use of the ceramic tile in public space and home room is more and more extensive, still, most of ceramic tile is only
Only have decoration functions.Therefore, how far infrared emission function organically to be combined with ceramic tile, becomes ceramic tile field
Very popular research topic.
Invention content
The main object of the present invention is to provide a kind of preparation method of far infrared ceramic tile, it is intended to so that ceramic tile has far infrared
Line emission function.
To achieve the above object, the preparation method of far infrared ceramic tile proposed by the present invention, includes the following steps:
Blank forming, and under conditions of green body is placed in 150 DEG C -200 DEG C, dry 70min-100min;
Billet surface after the drying applies far infrared ground-coat enamel, and is placed in 150 DEG C -250 by the green body after far infrared ground-coat enamel is applied
Under conditions of DEG C, dry 1min-5min;
Far infrared overglaze is applied on far infrared ground-coat enamel surface after the drying, and is placed in 150 by the green body after far infrared overglaze is applied
Under conditions of DEG C -250 DEG C, dry 1min-5min;
It will apply under conditions of the green body after far infrared ground-coat enamel and far infrared overglaze is placed in 1170 DEG C -1240 DEG C, fire
70min-75min obtains semi-finished product;
Using the polish line for including resin grinding block and Elastic abrasive body, semi-finished product is polished, edging, obtains finished product;
Super clean bright processing is carried out to finished surface, so that the glossiness of finished surface is spent up to 85 degree -95 to get far infrared
Ceramic tile;
The component of the far infrared ground-coat enamel includes aluminium oxide, silica, calcium oxide, potassium oxide, magnesia, barium monoxide, remote
Infrared additive, styrene and trisiloxanes ethylene glycol;
The component of the far infrared overglaze includes aluminium oxide, silica, calcium oxide, potassium oxide, magnesia, barium monoxide, oxygen
Change sodium, far infrared additive, styrene and trisiloxanes ethylene glycol;
The component of the far infrared additive includes kaolin, feldspar, quartz, nano-tourmaline, zirconium carbide, titanium dioxide
Zirconium.
Optionally, in the step of billet surface after the drying applies far infrared ground-coat enamel, the far infrared ground-coat enamel
Flow velocity is 28s-32s, and the proportion of the far infrared ground-coat enamel is 1.85g/ml-1.95g/ml, the applied amount of the far infrared ground-coat enamel
For 450g/m2-470g/m2, the fineness of the far infrared ground-coat enamel is that siccative weight percent is 0.4%- after 325 mesh sieve
0.6%.
Optionally, in the step of far infrared overglaze is applied on the far infrared ground-coat enamel surface after the drying, the far infrared
The flow velocity of overglaze is 28s-32s, and the proportion of the far infrared overglaze is 1.85g/ml-1.95g/ml, the far infrared overglaze
Applied amount is 1005g/m2-1020g/m2。
Optionally, the component of the nano-tourmaline includes:
Nanometer schorl 50w%-75w%;
Nanometer elbaite 12w%-45w%;
Nanometer dravite 3w%-25w%.
Optionally, the nano-tourmaline is modified Nano tourmaline.
Optionally, in the component of the far infrared ground-coat enamel, the mass ratio of the styrene and the trisiloxanes ethylene glycol
For (1-2):5;
And/or in the component of the far infrared overglaze, the mass ratio of the styrene and the trisiloxanes ethylene glycol is
(1-2):5。
Optionally, the component of the far infrared ground-coat enamel further includes fatty alcohol sulfonate and silanol class non-ionic surface active
Agent;
And/or the component of the far infrared overglaze further includes fatty alcohol sulfonate and silanol class nonionic surfactant.
Optionally, the mass fraction of each component of the far infrared ground-coat enamel is:
Optionally, the mass fraction of each component of the far infrared overglaze is:
Optionally, the resin grinding block includes:The resin grinding block of the resin grinding block and 3 group of 180 mesh of 5 group of 150 mesh;
The Elastic abrasive body includes:The bullet of the Elastic abrasive body of 5 group of 180 mesh, the Elastic abrasive body of 10 group of 240 mesh, 5 group of 300 mesh
Property abrading block, the elastic abrading block of 5 group of 400 purpose, the Elastic abrasive body of 5 group of 600 mesh, the Elastic abrasive body of 3 group of 800 mesh, 3 group of 1000 purpose
The Elastic abrasive body of Elastic abrasive body, the Elastic abrasive body of 3 group of 1500 mesh, the Elastic abrasive body of 3 group of 2000 mesh, 4 group of 3000 mesh.
Technical scheme of the present invention adds far infrared additive in the component of glaze (ground-coat enamel and overglaze), this is remote red
Tourmaline in external additive has far infrared emission function, also, its far infrared emission function subtracting with its grain size
Trend that is small and being in enhancing, the present invention is using nano-tourmaline, it is possible to understand that, it may make glaze and apply the glaze
The ceramic tile of material has excellent far infrared emission function, simultaneously as nano-tourmaline itself is also with a series of excellent
Surface, interface performance are conducive to its dispersion and homogenization in glaze, to further promote glaze and apply the glaze
Ceramic tile far infrared emission function strength and stability.
Also, in the far infrared additive, zirconium dioxide also has far infrared emission function, meanwhile, zirconium carbide is not
Only can efficient absorption visible light, be also equipped with far infrared reflection characteristic.The two with nano-tourmaline when coordinating, nano-tourmaline
The far infrared discharged with zirconium dioxide may make glaze and using the glaze after the zirconium carbide reflection of disperse
Ceramic tile has broader far infrared launch angle and more stable far infrared transmission power.
Also, technical scheme of the present invention is added with kaolin, feldspar and stone also in the component of far infrared additive
English, kaolin, which can play the role of optimization glaze suspension and wearability, feldspar, can play fluxing effect, and quartz can be played and be carried
For the effect of glaze skeleton structure.
Also, glaze (the ground-coat enamel and overglaze) component for adding far infrared additive can promote generation bubble in glaze
May, to influence final product effect.
Therefore, further, technical scheme of the present invention adds styrene and trisiloxanes second in the component of glaze
Glycol.Trisiloxanes ethylene glycol has higher surface-active, can spontaneously enter bubble surface layer, and between foam
It rapidly sprawls, repels the surfactant that foam surface layer is stabilized, avoid the self-repair function of tissue liquid film.That is, working as glaze
It is added after trisiloxanes ethylene glycol in the component of material, the molecule of trisiloxanes ethylene glycol can be widely distributed in the table of liquid
Face can be more than 90 ° since the molecule of trisiloxanes ethylene glycol has stronger hydrophobicity with the contact angle of foaming drop,
To force foaming drop to arrange rapidly, draws local rapid drainage foamy and cause to rupture, and bullet on liquid level can be inhibited
The generation of property film, terminates the generation of foam.That is, after trisiloxanes ethylene glycol is added in the component of glaze, molecule can
Foam surface is interspersed among immediately, and rapidly drawout comes, form very thin double film layers.Also, its molecule can further spread,
Infiltration, stratiform invasion, to replace the thin-walled of former foam, since the lower trisiloxanes glycol molecule of surface tension is in gas-
Liquid constantly spreads between interface, permeates, and keeps the membranous wall of bubble thinning rapidly, while bubble also suffers from the bubble surface of surrounding
The draw of power film layer strength, causes bubble ambient stress unbalance, so as to cause its " brokenly bubble ".
Also, the addition of styrene can be copolymerized crosslinking with trisiloxanes ethylene glycol and be formed by curing three-dimensional crosslinking
Reticular structure, to trisiloxanes ethylene glycol formed space protection effect, make it have the hydrolytic stability of height, stablize
The performance of trisiloxanes ethylene glycol defoaming effect.Also, it is also sustainable to ensure three since styrene is to the inertia of hydrolysis
The highly hydrolyzed stability of silicone glycol.
To sum up, technical scheme of the present invention not only may make ceramic tile to have far infrared emission function, but also by adding
Enter styrene and trisiloxanes ethylene glycol, effectively reduces the possibility that bubble generates in glaze, avoid caused by bubble
Glaze planar defect avoids the harmful effect that glaze planar defect emits ceramic tile far infrared, to improve the far infrared of ceramic tile
Emission function improves ceramic tile quality.
In addition, technical scheme of the present invention may make ceramic tile also by being above-mentioned steps by the optimum preparation condition of ceramic tile
Production process in, glaze can be aoxidized adequately, is burnt into, and to make extra gas be efficiently exhausted, be reduced
The glaze planar defects such as solution cavity, pin hole, glaze bubble, improve the quality of ceramic tile.
Description of the drawings
In order to more clearly explain the embodiment of the invention or the technical proposal in the existing technology, to embodiment or will show below
There is attached drawing needed in technology description to be briefly described, it should be apparent that, the accompanying drawings in the following description is only this
Some embodiments of invention for those of ordinary skill in the art without creative efforts, can be with
The structure shown according to these attached drawings obtains other attached drawings.
Fig. 1 is the flow diagram of one embodiment of preparation method of far infrared ceramic tile of the present invention.
The embodiments will be further described with reference to the accompanying drawings for the realization, the function and the advantages of the object of the present invention.
Specific implementation mode
Below in conjunction with Figure of description, preferred embodiment of the present invention will be described, it should be understood that described herein
Preferred embodiment only for the purpose of illustrating and explaining the present invention and is not intended to limit the present invention, and in the absence of conflict, this hair
The feature in embodiment and embodiment in bright can be combined with each other.
As shown in Figure 1, the present invention proposes a kind of preparation method of far infrared ceramic tile, include the following steps:
Step S10, blank forming, and under conditions of green body is placed in 150 DEG C -200 DEG C, dry 70min-100min;
Step S20, billet surface after the drying apply far infrared ground-coat enamel, and are placed in the green body after far infrared ground-coat enamel is applied
Under conditions of 150 DEG C -250 DEG C, dry 1min-5min;
Far infrared overglaze is applied on step S30, far infrared ground-coat enamel surface after the drying, and will apply the green body after far infrared overglaze
It is placed under conditions of 150 DEG C -250 DEG C, dry 1min-5min;
Step S40 will be applied under conditions of the green body after far infrared ground-coat enamel and far infrared overglaze is placed in 1170 DEG C -1240 DEG C,
70min-75min is fired, semi-finished product are obtained;
Step S50 is polished semi-finished product using the polish line for including resin grinding block and Elastic abrasive body, edging, obtains
Finished product;
Step S60 carries out super clean bright processing to finished surface, so that the glossiness of finished surface is spent up to 85 degree -95, i.e.,
Obtain far infrared ceramic tile;
The component of the far infrared ground-coat enamel includes aluminium oxide, silica, calcium oxide, potassium oxide, magnesia, barium monoxide, remote
Infrared additive, styrene and trisiloxanes ethylene glycol;
The component of the far infrared overglaze includes aluminium oxide, silica, calcium oxide, potassium oxide, magnesia, barium monoxide, oxygen
Change sodium, far infrared additive, styrene and trisiloxanes ethylene glycol;
The component of the far infrared additive includes kaolin, feldspar, quartz, nano-tourmaline, zirconium carbide, titanium dioxide
Zirconium.
First, technical scheme of the present invention adds far infrared additive in the component of glaze (ground-coat enamel and overglaze), should
Tourmaline in far infrared additive has far infrared emission function, also, its far infrared emission function is with its grain size
Reduction and in enhancing trend, the present invention is using nano-tourmaline, it is possible to understand that, may make glaze and application
The ceramic tile of the glaze has excellent far infrared emission function, simultaneously as nano-tourmaline itself is also with a series of excellent
Different surface, interface performance, are conducive to its dispersion and homogenization in glaze, should to further promote glaze and application
The strength and stability of the far infrared emission function of the ceramic tile of glaze.
Also, in the far infrared additive, zirconium dioxide also has far infrared emission function, meanwhile, zirconium carbide is not
Only can efficient absorption visible light, be also equipped with far infrared reflection characteristic.The two with nano-tourmaline when coordinating, nano-tourmaline
The far infrared discharged with zirconium dioxide may make glaze and using the glaze after the zirconium carbide reflection of disperse
Ceramic tile has broader far infrared launch angle and more stable far infrared transmission power.
Also, technical scheme of the present invention is added with kaolin, feldspar and stone also in the component of far infrared additive
English, kaolin, which can play the role of optimization glaze suspension and wearability, feldspar, can play fluxing effect, and quartz can be played and be carried
For the effect of glaze skeleton structure.
Also, glaze (the ground-coat enamel and overglaze) component for adding far infrared additive can promote generation bubble in glaze
May, to influence final product effect.
Therefore, further, technical scheme of the present invention adds styrene and trisiloxanes second in the component of glaze
Glycol.Trisiloxanes ethylene glycol has higher surface-active, can spontaneously enter bubble surface layer, and between foam
It rapidly sprawls, repels the surfactant that foam surface layer is stabilized, avoid the self-repair function of tissue liquid film.That is, working as glaze
It is added after trisiloxanes ethylene glycol in the component of material, the molecule of trisiloxanes ethylene glycol can be widely distributed in the table of liquid
Face can be more than 90 ° since the molecule of trisiloxanes ethylene glycol has stronger hydrophobicity with the contact angle of foaming drop,
To force foaming drop to arrange rapidly, draws local rapid drainage foamy and cause to rupture, and bullet on liquid level can be inhibited
The generation of property film, terminates the generation of foam.That is, after trisiloxanes ethylene glycol is added in the component of glaze, molecule can
Foam surface is interspersed among immediately, and rapidly drawout comes, form very thin double film layers.Also, its molecule can further spread,
Infiltration, stratiform invasion, to replace the thin-walled of former foam, since the lower trisiloxanes glycol molecule of surface tension is in gas-
Liquid constantly spreads between interface, permeates, and keeps the membranous wall of bubble thinning rapidly, while bubble also suffers from the bubble surface of surrounding
The draw of power film layer strength, causes bubble ambient stress unbalance, so as to cause its " brokenly bubble ".
Also, the addition of styrene can be copolymerized crosslinking with trisiloxanes ethylene glycol and be formed by curing three-dimensional crosslinking
Reticular structure, to trisiloxanes ethylene glycol formed space protection effect, make it have the hydrolytic stability of height, stablize
The performance of trisiloxanes ethylene glycol defoaming effect.Also, it is also sustainable to ensure three since styrene is to the inertia of hydrolysis
The highly hydrolyzed stability of silicone glycol.
To sum up, technical scheme of the present invention not only may make ceramic tile to have far infrared emission function, but also by adding
Enter styrene and trisiloxanes ethylene glycol, effectively reduces the possibility that bubble generates in glaze, avoid caused by bubble
Glaze planar defect avoids the harmful effect that glaze planar defect emits ceramic tile far infrared, to improve the far infrared of ceramic tile
Emission function improves ceramic tile quality.
In addition, technical scheme of the present invention may make ceramic tile also by being above-mentioned steps by the optimum preparation condition of ceramic tile
Production process in, glaze can be aoxidized adequately, is burnt into, and to make extra gas be efficiently exhausted, be reduced
The glaze planar defects such as solution cavity, pin hole, glaze bubble, improve the quality of ceramic tile.
Preferably, in the step of billet surface after the drying applies far infrared ground-coat enamel, the far infrared ground-coat enamel
Flow velocity is 28s-32s, and the proportion of the far infrared ground-coat enamel is 1.85g/ml-1.95g/ml, the applied amount of the far infrared ground-coat enamel
For 450g/m2-470g/m2, the fineness of the far infrared ground-coat enamel is that siccative weight percent is 0.4%- after 325 mesh sieve
0.6%.In this way, can the adhesive strength of ground-coat enamel and green body effectively be promoted, and ensure the application stability of overglaze on ground-coat enamel so that
Glaze is able to good oxidation, firing, reduces the glaze planar defects such as solution cavity, pin hole, glaze bubble, reduces these glaze planar defects to far infrared
The obstruction of line transmitting promotes the strength and stability of the far infrared transmitting of ground-coat enamel, overglaze and ceramic tile.
Preferably, in the step of far infrared overglaze is applied on the far infrared ground-coat enamel surface after the drying, the far infrared
The flow velocity of overglaze is 28s-32s, and the proportion of the far infrared overglaze is 1.85g/ml-1.95g/ml, the far infrared overglaze
Applied amount is 1005g/m2-1020g/m2.In this way, not only can effectively promote the adhesive strength of overglaze, the remote of overglaze and ceramic tile is ensured
Infrared ray transmitting function, but also the glaze planar defects such as solution cavity, pin hole, glaze bubble can be effectively reduced, to effectively reduce these glazes
The obstruction that defect emits far infrared promotes the strength and stability of the far infrared transmitting of ground-coat enamel, overglaze and ceramic tile.
Specifically, the mass fraction of each component of the far infrared overglaze is:
Wherein, the mass fraction of each component of the far infrared additive is:
In this way, by the optimization of formula and dosage to far infrared overglaze, that is, the formulation content of aluminium oxide is improved, reduced
The formulation content with melting behaviour such as calcium oxide, magnesia lacks in this way, the glazes such as solution cavity, pin hole, glaze bubble can be effectively reduced
It falls into, improves the quality of overglaze and ceramic tile.
Preferably, the mass ratio of the styrene and the trisiloxanes ethylene glycol is (1-2):5.
In this way, the synergistic effect between styrene and trisiloxanes ethylene glycol not only may make to be maintained at higher level, subtract
The bubble and defect in overglaze are lacked, also can effectively avoid the raising of overglaze surface tension, overglaze is avoided to reunite, ensure overglaze
Uniformity, to effective guarantee overglaze and the far infrared emission function of ceramic tile.
Further, the component of the far infrared overglaze further includes fatty alcohol sulfonate and silanol class non-ionic surface active
Agent.Specifically, the silanol class nonionic surfactant is triphenyl silicone.
Due to the addition of overglaze component mid and far infrared additive, the case where exacerbating overglaze surface tension unbalance stress, cause
The problem of making overglaze reunite.Therefore, technical scheme of the present invention also adds fatty alcohol sulfonate in the component of overglaze
With silanol class nonionic surfactant.Since fatty alcohol sulfonate has longer hydrophobic grouping-aliphatic chain hydroxyl, also,
Chain length is longer, and the dynamics stretched out to surface layer overglaze is bigger, reduces with joint efforts suffered by the overglaze of surface layer to may make so that overglaze
Surface tension be minimized.
At the same time, silanol class nonionic surfactant does not occur ionization in overglaze and exists in the form of molecule,
Its stability is high, is not easy to be influenced by strong electrolyte inorganic salts and pH value.At this point, silanol class nonionic surfactant molecule
In lipophilic group it is roughly the same with the lipophilic group of ionic surfactant, but its hydrophilic radical then mainly by having
A certain number of oxygen-containing groups (such as hydroxyl and polyoxyethylene chain) are constituted:Lipophilic group is attached to the surface of solids, hydrophilic radical to
It stretches in liquid outside, so that the reduction in surface tension of overglaze, and then the mobility of overglaze is effectively increased, improve density
The uniformity of distribution.
Also, silanol class nonionic surfactant also has mutual promoting action with fatty alcohol sulfonate, can not only have
Effect promotes dispersibility, uniformity of the two in overglaze, also may make that the two increases the reducing effect of overglaze surface tension
By force.
In addition, silanol class nonionic surfactant also has the characteristics that low foaming characteristic, bubble in overglaze is effectively reduced
Generation, improve the quality of product.
Further, in order to effectively promoted fatty alcohol sulfonate and silanol class nonionic surfactant it is respective effect with
And its common cooperation, the mass fraction of the fatty alcohol sulfonate is 5w%-8w%, the silanol class non-ionic surface active
The mass fraction of agent is 0.3w%-2w%.
Preferably, the hydrophilic-hydrophobic balance value of the fatty alcohol sulfonate is 8-10, and the silanol class non-ionic surface is lived
Property agent hydrophilic-hydrophobic balance value be 9-16.
At this point, the hydrophilic-hydrophobic balance value of fatty alcohol sulfonate and silanol class nonionic surfactant is 10 or so,
In this way, may make fatty alcohol sulfonate and silanol class nonionic surfactant that both there is preferable hydrophily, it may have preferably
Lipophile so that fatty alcohol sulfonate and silanol class nonionic surfactant can further decrease the surface of overglaze
Tension so that the mobility of overglaze and further being promoted for uniformity reduce possibility, promotion overglaze that overglaze bubble generates
With the bond strength of ground-coat enamel.
Specifically, the mass fraction of each component of the far infrared ground-coat enamel is:
Wherein, the mass fraction of each component of the far infrared additive is:
In this way, by the optimization of formula and dosage to far infrared ground-coat enamel, that is, the formulation content of aluminium oxide is improved, reduced
The formulation content with melting behaviour such as calcium oxide, magnesia lacks in this way, the glazes such as solution cavity, pin hole, glaze bubble can be effectively reduced
It falls into, improves the quality of ground-coat enamel and ceramic tile.
Preferably, the mass ratio of the styrene and the trisiloxanes ethylene glycol is (1-2):5.
In this way, the synergistic effect between styrene and trisiloxanes ethylene glycol not only may make to be maintained at higher level, subtract
The bubble and defect in ground-coat enamel are lacked, also can effectively avoid the raising of ground-coat enamel surface tension, ground-coat enamel is avoided to reunite, ensure ground-coat enamel
Uniformity, to effective guarantee ground-coat enamel and the far infrared emission function of ceramic tile.
Further, the component of the far infrared ground-coat enamel further includes fatty alcohol sulfonate and silanol class non-ionic surface active
Agent.Specifically, the silanol class nonionic surfactant is triphenyl silicone.
Due to the addition of ground-coat enamel component mid and far infrared additive, the case where exacerbating ground-coat enamel surface tension unbalance stress, cause
The problem of making ground-coat enamel reunite.Therefore, technical scheme of the present invention also adds fatty alcohol sulfonate in the component of ground-coat enamel
With silanol class nonionic surfactant.Since fatty alcohol sulfonate has longer hydrophobic grouping-aliphatic chain hydroxyl, also,
Chain length is longer, and the dynamics stretched out to surface layer ground-coat enamel is bigger, reduces with joint efforts suffered by the ground-coat enamel of surface layer to may make so that ground-coat enamel
Surface tension be minimized.
At the same time, silanol class nonionic surfactant does not occur ionization in ground-coat enamel and exists in the form of molecule,
Its stability is high, is not easy to be influenced by strong electrolyte inorganic salts and pH value.At this point, silanol class nonionic surfactant molecule
In lipophilic group it is roughly the same with the lipophilic group of ionic surfactant, but its hydrophilic radical then mainly by having
A certain number of oxygen-containing groups (such as hydroxyl and polyoxyethylene chain) are constituted:Lipophilic group is attached to the surface of solids, hydrophilic radical to
It stretches in liquid outside, so that the reduction in surface tension of ground-coat enamel, and then the mobility of ground-coat enamel is effectively increased, improve density
The uniformity of distribution.
Also, silanol class nonionic surfactant also has mutual promoting action with fatty alcohol sulfonate, can not only have
Effect promotes dispersibility, uniformity of the two in ground-coat enamel, also may make that the two increases the reducing effect of ground-coat enamel surface tension
By force.
In addition, silanol class nonionic surfactant also has the characteristics that low foaming characteristic, bubble in ground-coat enamel is effectively reduced
Generation, improve the quality of product.
Further, in order to effectively promoted fatty alcohol sulfonate and silanol class nonionic surfactant it is respective effect with
And its common cooperation, the mass fraction of the fatty alcohol sulfonate is 3w%-7w%, the silanol class non-ionic surface active
The mass fraction of agent is 0.1w%-1w%.
Preferably, the hydrophilic-hydrophobic balance value of the fatty alcohol sulfonate is 8-10, and the silanol class non-ionic surface is lived
Property agent hydrophilic-hydrophobic balance value be 9-16.
At this point, the hydrophilic-hydrophobic balance value of fatty alcohol sulfonate and silanol class nonionic surfactant is 10 or so,
In this way, may make fatty alcohol sulfonate and silanol class nonionic surfactant that both there is preferable hydrophily, it may have preferably
Lipophile so that fatty alcohol sulfonate and silanol class nonionic surfactant can further decrease the surface of ground-coat enamel
Tension so that the mobility of ground-coat enamel and further being promoted for uniformity reduce possibility, promotion ground-coat enamel that ground-coat enamel bubble generates
With the bond strength of green body.
Further, whether in the formula of far infrared overglaze, or in the formula of far infrared ground-coat enamel, the nanometer
Tourmaline is modified Nano tourmaline.
Specifically, modifying process is as follows:According to mass fraction meter, 0.3 part of -0.5 part of phthalic acid is added 300 part -380
In part deionized water, stirring is warming up to 70 DEG C -80 DEG C, adds 6 parts of -10 parts of nano-tourmalines, stirs 10min-15min, according to
0.1-0.2 parts of manganese powders of secondary addition and 0.05-0.22 parts of molybdenum powders, are continuously heating to 85 DEG C -90 DEG C, constant temperature at the uniform velocity stirs 45min-
55min is continuously heating to 100-110 DEG C, sequentially add 0.3 part of -0.5 part of nano calcium oxide, 0.15 part -0.3 part it is nano oxidized
Zinc, 0.8 part of -1 part of nano barium carbonate, 0.1 part of -0.2 part of nanometer titanium silicate, constant temperature at the uniform velocity stir 1h-2h, stop reaction, filter,
Filter residue is taken, it is dry to get modified Nano tourmaline.
In the above process, the deionized water of nano-tourmaline particle and its adsorption occurs dissociation and forms hydroxyl, benzene two
Esterification occurs for the great amount of hydroxy group of carboxyl and nano-tourmaline particle surface in formic acid, and in nano-tourmaline particle surface
Monomolecular film is formed, i.e., surface modification is carried out to nano-tourmaline particle so that nano-tourmaline particle surface is by dipole inversion
At nonpolarity, polarity is reduced.Also, the monomolecular film that nano-tourmaline particle surface generates can also reduce nano-tourmaline
Interaction force between particle surface improves the mobility of modified Nano tourmaline.In addition, the carboxyl that phthalic acid provides
There is electrostatic repulsion as anion, additionally it is possible to the molecular dispersivity in system, uniformity be made further to be promoted.
In this way, dispersibility and uniformity of the modified Nano tourmaline in glaze (ground-coat enamel and overglaze) are effectively improved, this
Sample not only can effectively enhance the far infrared emission function of glaze and ceramic tile, widen the far infrared angle of departure of glaze and ceramic tile
Degree promotes the stability of glaze and the transmitting of ceramic tile far infrared;And the polarity of modified nano-tourmaline particle surface compared with
Low, dispersibility, uniformity are extremely strong, also can effectively avoid the generation of agglomeration in glaze, reduce the glaze such as solution cavity, pin hole, glaze bubble
Planar defect, to effectively improve the quality of glaze and ceramic tile.
At this point, the nano-tourmaline in glaze uses modified Nano tourmaline, the negative of nano-tourmaline can be also effectively improved
Ion release assigns the good anion function of ceramic tile using the glaze.
Specifically, the nano-tourmaline includes in a nanometer schorl, nanometer elbaite and nanometer dravite
It is at least one.That is, carry out nano-tourmaline selection when, both can independent choice nanometer schorl, nanometer elbaite and
Nanometer any one of dravite, also can be in simultaneous selection nanometer schorl, nanometer elbaite and nanometer dravite
Any two, can also nanometer schorl, nanometer elbaite and nanometer dravite three's simultaneous selection.
Preferably, the component of the nano-tourmaline includes:
Nanometer schorl 50w%-75w%;
Nanometer elbaite 12w%-45w%;
Nanometer dravite 3w%-25w%.
At this point, the nano-particle of a variety of crystallographic systems is contained in nano-tourmaline, and when such nano-tourmaline is scattered in
When in glaze, the nano-particle of a variety of crystallographic systems can form random spread pattern, not only effectively reduce solution cavity, pin hole, glaze
The glaze planar defects such as bubble, but also the bond strength between overglaze and ground-coat enamel, ground-coat enamel and idiosome is effectively enhanced, to effectively be promoted
The quality of glaze and ceramic tile.
Preferably, the resin grinding block includes:The resin grinding block of the resin grinding block and 3 group of 180 mesh of 5 group of 150 mesh;
The Elastic abrasive body includes:The bullet of the Elastic abrasive body of 5 group of 180 mesh, the Elastic abrasive body of 10 group of 240 mesh, 5 group of 300 mesh
Property abrading block, the elastic abrading block of 5 group of 400 purpose, the Elastic abrasive body of 5 group of 600 mesh, the Elastic abrasive body of 3 group of 800 mesh, 3 group of 1000 purpose
The Elastic abrasive body of Elastic abrasive body, the Elastic abrasive body of 3 group of 1500 mesh, the Elastic abrasive body of 3 group of 2000 mesh, 4 group of 3000 mesh.
Specifically, the quantity of resin grinding block is 6 in each group of resin module, elastic module in each group of elastic module
Quantity is 6.
Resin grinding block is arranged in before Elastic abrasive body, i.e., ceramic tiles in advance passes through the grinding process of each group resin grinding block, using
The grinding process of each group Elastic abrasive body.Also, when by each group resin grinding block, ceramic tiles in advance passes through the group of low mesh number, then passes through
Cross the group of high mesh number;When by each group Elastic abrasive body, ceramic tiles in advance passes through the group of low mesh number, using the group of high mesh number
Not.
In this way, may make that the surface of ceramic tile is more smooth, bright and clean, so as to effectively reduce overglaze surface impurity, spot etc.
The residual of substance, slows down erosion and destruction of the substances such as impurity, spot to overglaze, and then effectively promotes the remote red of overglaze and ceramic tile
The stability and persistence of outside line emission function.
The foregoing is merely the preferred embodiment of the present invention, are not intended to limit the scope of the invention, every at this
Under the inventive concept of invention, using equivalent structure transformation made by description of the invention and accompanying drawing content, or directly/use indirectly
In the scope of patent protection that other related technical areas are included in the present invention.
Claims (10)
1. a kind of preparation method of far infrared ceramic tile, which is characterized in that include the following steps:
Blank forming, and under conditions of green body is placed in 150 DEG C -200 DEG C, dry 70min-100min;
Billet surface after the drying applies far infrared ground-coat enamel, and is placed in 150 DEG C -250 DEG C by the green body after far infrared ground-coat enamel is applied
Under the conditions of, dry 1min-5min;
Far infrared overglaze is applied on far infrared ground-coat enamel surface after the drying, and will apply the green body after far infrared overglaze be placed in 150 DEG C-
Under conditions of 250 DEG C, dry 1min-5min;
It will apply under conditions of the green body after far infrared ground-coat enamel and far infrared overglaze is placed in 1170 DEG C -1240 DEG C, fire 70min-
75min obtains semi-finished product;
Using the polish line for including resin grinding block and Elastic abrasive body, semi-finished product is polished, edging, obtains finished product;
Super clean bright processing is carried out to finished surface, so that the glossiness of finished surface is spent up to 85 degree -95 to get far infrared ceramic tile;
The component of the far infrared ground-coat enamel includes aluminium oxide, silica, calcium oxide, potassium oxide, magnesia, barium monoxide, far infrared
Additive, styrene and trisiloxanes ethylene glycol;
The component of the far infrared overglaze include aluminium oxide, silica, calcium oxide, potassium oxide, magnesia, barium monoxide, sodium oxide molybdena,
Far infrared additive, styrene and trisiloxanes ethylene glycol;
The component of the far infrared additive includes kaolin, feldspar, quartz, nano-tourmaline, zirconium carbide, zirconium dioxide.
2. preparation method as described in claim 1, which is characterized in that apply far infrared bottom in the billet surface after the drying
In the step of glaze, the flow velocity of the far infrared ground-coat enamel is 28s-32s, and the proportion of the far infrared ground-coat enamel is 1.85g/ml-
The applied amount of 1.95g/ml, the far infrared ground-coat enamel are 450g/m2-470g/m2, the fineness of the far infrared ground-coat enamel is through 325 mesh
Siccative weight percent is 0.4%-0.6% after sieve.
3. preparation method as described in claim 1, which is characterized in that applied far on the far infrared ground-coat enamel surface after the drying
In the step of infrared overglaze, the flow velocity of the far infrared overglaze is 28s-32s, and the proportion of the far infrared overglaze is 1.85g/
The applied amount of ml-1.95g/ml, the far infrared overglaze are 1005g/m2-1020g/m2。
4. preparation method as described in claim 1, which is characterized in that the component of the nano-tourmaline includes:
Nanometer schorl 50w%-75w%;
Nanometer elbaite 12w%-45w%;
Nanometer dravite 3w%-25w%.
5. preparation method as described in claim 1, which is characterized in that the nano-tourmaline is modified Nano tourmaline.
6. preparation method as described in claim 1, which is characterized in that in the component of the far infrared ground-coat enamel, the styrene
Mass ratio with the trisiloxanes ethylene glycol is (1-2):5;
And/or in the component of the far infrared overglaze, the mass ratio of the styrene and the trisiloxanes ethylene glycol is (1-
2):5。
7. preparation method as described in claim 1, which is characterized in that the component of the far infrared ground-coat enamel further includes fatty alcohol sulphur
Hydrochlorate and silanol class nonionic surfactant;
And/or the component of the far infrared overglaze further includes fatty alcohol sulfonate and silanol class nonionic surfactant.
8. preparation method as described in claim 1, which is characterized in that the mass fraction of each component of the far infrared ground-coat enamel
For:
9. preparation method as described in claim 1, which is characterized in that the mass fraction of each component of the far infrared overglaze
For:
10. preparation method as described in claim 1, which is characterized in that the resin grinding block includes:The resin mill of 5 group of 150 mesh
The resin grinding block of block and 3 group of 180 mesh;
The Elastic abrasive body includes:The elasticity mill of the Elastic abrasive body of 5 group of 180 mesh, the Elastic abrasive body of 10 group of 240 mesh, 5 group of 300 mesh
The elasticity of block, the elastic abrading block of 5 group of 400 purpose, the Elastic abrasive body of 5 group of 600 mesh, the Elastic abrasive body of 3 group of 800 mesh, 3 group of 1000 mesh
The Elastic abrasive body of abrading block, the Elastic abrasive body of 3 group of 1500 mesh, the Elastic abrasive body of 3 group of 2000 mesh, 4 group of 3000 mesh.
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| CN105541410A (en) * | 2016-02-02 | 2016-05-04 | 福建省威尔陶瓷股份有限公司 | Modified tourmaline powder for ceramic glaze, anion ceramic glaze and preparation method |
| CN106007377A (en) * | 2016-05-20 | 2016-10-12 | 河源市东源鹰牌陶瓷有限公司 | Super-flat glazed brick |
| CN107163294A (en) * | 2017-06-07 | 2017-09-15 | 深圳市创艺工业技术有限公司 | A kind of far infrared composite powder |
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| CN102515703A (en) * | 2011-12-20 | 2012-06-27 | 四川新中源陶瓷有限公司 | Production technology of super-flat high-crystal stone tile |
| CN104829133A (en) * | 2015-03-30 | 2015-08-12 | 佛山市新战略知识产权文化有限公司 | Negative ion ceramic glaze and method for preparation of negative ion ceramic brick from negative ion ceramic glaze |
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