CN106348603A

CN106348603A - Low temperature antique glaze with cleaner air effect and preparing method thereof

Info

Publication number: CN106348603A
Application number: CN201610749357.9A
Authority: CN
Inventors: 黎淑娟
Original assignee: Foshan Gaoming Technology Co Ltd
Current assignee: Foshan Gaoming Technology Co Ltd
Priority date: 2016-08-29
Filing date: 2016-08-29
Publication date: 2017-01-25

Abstract

The invention discloses a low temperature antique glaze with cleaner air effect and preparing method thereof, the preparing method comprises the steps of: A, preparing low temperature frit; B, preparing glaze, mixing low temperature frit, colorant, potassium feldspar, quartz, calcite, talc, calcium phosphate, anion compounds and antibacterial composite to obtain the mixing powder, putting sodium tripolyphosphate and carboxymethyl cellulose into powder and mixing the powder evenly, fine grinding, and then adding water so as to obtain the glaze; C, applying the glaze evenly on the body, and then putting the body into the reducing atmosphere furnace, cooling the natural glaze to room temperature after heat preservation, and the low temperature antique glaze with cleaner air effect is obtained. Compared with the prior antique glaze, the antique glaze produced by the invention has the advantages of scientific ingredients,reasonable preparing method, pure color and stable performance; at the same time with a reasonable combination of negative ions and antibacterial composite materials, the synergistic action of the two making the antique glaze has characteristics of excellent anti-bacterial, anti-fouling and air purification, the scope of the application of the antique glaze is further broaden.

Description

A kind of have low temperature glaze modelled after an antique of purify air effect and preparation method thereof

Technical field

The present invention relates to ceramic technology field, a kind of more particularly to low temperature glaze modelled after an antique with purify air effect And preparation method thereof.

Background technology

Antibacterial, mycete has very big harm as pathogen to the mankind and animals and plants, and the health of impact people even jeopardizes life Life, brings great economic loss.The research of therefore anti-biotic material and its product increasingly causes the concern of people, antibacterial product Demand will constitute huge market.

For environmental conservation aspect, negative aeroion can eliminate foreign flavor indoors and various harmful gass.Fit up indoors Leftovers leftovers in the irritative gass such as benzene that used in process, art work evaporates, formaldehyde, ketone, ammonia and daily life Acid smell, the harmful abnormal flavour such as medicated cigarette, with the material rich in anion, the negative aeroion of its release can be effectively Eliminated, reached the purpose of purify air, and had good suppression to golden staphylococci, escherichia coli, candidiasises and mycete etc. Make and use.

With economic fast development and people to growth in the living standard, ceramic has become as people family, does The ornamental pottery in the places such as public room, market, but the existing Ceramic glaze having technology is although smoothness is high, various colors, but It is that pottery modelled after an antique is less, particularly multi-functional glaze modelled after an antique, substantially without reference to therefore technology has much room for improvement, and needs research and development function badly Type glaze modelled after an antique, the such as function such as antibacterial, antistatic, purify air, widen its range of application further.

Content of the invention

In order to solve above-mentioned the deficiencies in the prior art, the invention provides a kind of low temperature with purify air effect is modelled after an antique Glaze and preparation method thereof.

The technical problem to be solved is achieved by the following technical programs:

A kind of have low temperature glaze modelled after an antique of purify air effect and preparation method thereof, and this preparation method comprises the following steps:

Step a, prepares anion low temperature frit: by 10 ~ 18% quartz, 5 ~ 12% Anhydrites, 15 ~ 25% Boraxs, 3 ~ 12% carbonate, 20 ~ 35% boric acid, 3 ~ 8% spodumenes, 1 ~ 4% fluoride salt, 0 ~ 5% Kaolin mixed grinding are uniform；Add 0 ~ 2% antibiotic complex and 1 ~ 8% anion complex, grinds and compound is uniformly obtained；Compound is dispensed in loading fire resistant sagger, carries out 1250 ~ 1320 DEG C High temperature melting, obtains the slurry of molten state；By slurry water quenching cooling, and it is broken into graininess, prepared anion low temperature frit；Its In, described Anhydrite is obtained by mixing by weight 4:1 by potassium feldspar and albite；Described carbonate is by potassium carbonate, sodium carbonate, carbonic acid Barium, lithium carbonate and Calcium Carbonate are obtained by mixing by weight 3:1:3:2:1；Described fluoride salt is by sodium fluoride, calcium fluoride and lithium fluoride It is obtained by mixing by weight 4:2:1；

Step b, prepares glaze slip: by mass percentage, will be long to 25 ~ 35% low temperature frits, 3 ~ 10% coloring agent, 30 ~ 40% potassium Stone, 10 ~ 20% quartz, 3 ~ 6% calcites, 3 ~ 6% Talcum, 2 ~ 5% calcium phosphate, 0 ~ 3% antibiotic complex and 1 ~ 8% anion Complex is mixed to get mixed-powder, adds sodium tripolyphosphate and carboxymethyl cellulose mix homogeneously, carefully in mixed-powder It is milled to 300 ~ 350 mesh, be subsequently adding water and obtain glaze slip and modulate glaze slip proportion for 1.6 ~ 1.7g/cm³；Wherein, sodium tripolyphosphate Addition is the 0.2 ~ 0.5% of mixed-powder quality, and the addition of carboxymethyl cellulose is the 2 ~ 3% of mixed-powder quality；

Step c, glaze slip is equably applied and applies on base substrate, then in reducing atmosphere stove, natural after being incubated at 700 ~ 800 DEG C It is cooled to room temperature, obtain anion low temperature glaze modelled after an antique.

Wherein, described coloring agent is the ultrafine slag that ferrum oxide or particle diameter are less than 200 mesh.Described ultrafine slag preparation process As follows: Iron-ore Slag is roughly ground to can be ground uniformly in mortar, then carried out ball milling, drum's speed of rotation after 60 ~ 80 mesh sieves For 1400 ~ 1600r/min, Ball-milling Time is 50 ~ 70min；Then 200 ~ 250 mesh sieves are crossed.

Wherein, described Anhydrite is obtained by mixing by weight 3 ~ 5:1 ~ 2 by potassium feldspar and albite.Described carbonate is by carbonic acid At least one composition in potassium, sodium carbonate, brium carbonate, lithium carbonate and Calcium Carbonate is it is preferable that described carbonate is by potassium carbonate, carbon Sour sodium, brium carbonate, lithium carbonate and Calcium Carbonate are obtained by mixing by weight 3:1:3:2:1.Described fluoride salt is by sodium fluoride, calcium fluoride It is obtained by mixing by weight 4:2:1 with lithium fluoride.

In the present invention, described anion complex preparation method is as follows: by 5 ~ 10% coral fossil, 10 ~ 15% tourmaline, 20 ~ 35% opals, 1 ~ 5% serpentine, 5 ~ 10% Maifanitums, 1 ~ 5% rare ice stone, 1 ~ 5% hokutolite, 1 ~ 5% Doctor king stone, 5 ~ 10% shellfishes Shell, 10 ~ 15% kieselguhr, 1 ~ 3% iron sesquioxide, 2 ~ 5% aluminium sesquioxide, 3 ~ 8% zirconium oxides and 1 ~ 5% zirconium phosphate mix homogeneously, Add in grinding equipment and carry out superfine grinding, until particle diameter distribution, in 50 ~ 80nm, is sieved, be dried, you can be obtained described negative Ion powder.5 ~ 10g anion powder is taken to be scattered in 100 ~ 200ml ultra-pure water, water bath sonicator 1 ~ 2h obtains all even stable dividing Dispersion liquid；When the substrate with carbon nanotube mesh film is placed in about 8 DEG C, dispersion liquid is added in the substrate of concave shape, meanwhile, Roll around roller, so that this homogeneous dispersion is scattered in this carbon nanotube mesh film, due to having when CNT is near 8 DEG C There is hydrophilic, this dispersion liquid is attracted to multiple net holes of carbon nanotube mesh film；It is warming up to about 25 DEG C, CNT has thin Aqueouss drive hydrone away leave behind anion powder and adsorb in multiple net holes of carbon nanotube mesh film；After drying, will inhale Carbon nanotube mesh film with anion powder scrapes off this substrate, obtains anion powder/CNT.

In the present invention, described antibiotic complex can be obtained by the following method:

(1) weigh 0.3 ~ 1gc60 powder, measure the concentrated sulphuric acid that 80 ~ 100ml mass fraction is 98%, by c60 powder and concentrated sulphuric acid Beaker mixes, beaker is placed in ice-water bath, stirred with the speed of 500 ~ 600rpm simultaneously, obtain mixed liquor；Weigh 1 ~ 3g high Potassium manganate powder, slowly adds in above-mentioned mixed liquor；Remove ice-water bath, change water-bath into, keep 30 ~ 40 DEG C of bath temperature, instead Answer 3 ~ 5h；Rapidly join 100 ~ 150ml pure water, filter, then dialysed 3 ~ 5 days with the bag filter that molecular cut off is 1000, obtain Graphene quantum dot (gqds) suspension；100 ~ 150rpm speed stirs gqds suspension, laser irradiation 30 ~ 60min simultaneously, swashs Photoirradiation power is 0.5 ~ 2w；Standby；

(2) ultrasonic agitation 50 ~ 60mlgqds suspension, Deca concentration is 0.001 ~ 0.01mol/l silver nitrate aqueous solution；Dropwise plus Enter concentration be 0.1 ~ 0.5mol/l ammonium dihydrogen phosphate (ammonium dihydrogen phosphate and silver nitrate aqueous solution volume ratio are 2 ~ 3: 1), ultrasonic agitation 10 ~ 20min；Be added dropwise over 0.5 ~ 1mol/l sodium hydroxide solution, adjust ph value to 11, then standing, from The heart, deionized water and ethanol replace washing three times, vacuum drying, obtain gqds/ag₂o；

(3) take 1 ~ 3ggqds/ag₂O ultrasonic agitation is scattered in 80 ~ 120ml aqueous solution；Be added dropwise over concentration be 0.005 ~ 0.05mol/l cerous nitrate aqueous solution, being added dropwise over concentration after 30 ~ 60min is 0.005 ~ 0.05mol/l zinc nitrate aqueous solution, gqds/ag₂O aqueous solution, cerous nitrate aqueous solution and zinc nitrate aqueous solution volume ratio are 1:0.1 ~ 0.2:0.2 ~ 0.4；Continue ultrasonic Stirring, regulation mixed solution ph value to 7.0；Side ultrasonic agitation, side adds the hydrazine hydrate that 4 ~ 8ml mass fraction is 50%, 30 ~ Reduction reaction 0.5 ~ 1h at 40 DEG C；Afterwards, the hydrazine hydrate that 40 ~ 50ml mass fraction is 50%, reduction reaction at 85 DEG C are added After 30 ~ 48h；Filter, be washed with deionized for several times, vacuum drying, obtain gqds/ag₂o/ag-zn-ce；

(4) by 0.1 ~ 0.5ggqds/ag₂O/ag-zn-ce ultrasonic agitation is scattered in aqueous solution；Add volume ratio 3 ~ 5:1 afterwards Water and ammonia, be stirring evenly and then adding into tetraethyl orthosilicate (with gqds/ag₂The mass ratio of o/ag-zn-ce is 3:1 ~ 3), adjust Ph value is 9 ~ 10, and reaction temperature is 20 ~ 25 DEG C, reacts 30 ~ 60min；Carry out being centrifuged and being cleaned with acetone and deionized water successively Obtain precipitation；This is deposited at 80 ~ 90 DEG C 2 ~ 4h is dried, to obtain gqds/ag₂o/ag-zn-ce/sio₂；By gqds/ ag₂o/ag-zn-ce/sio₂It is placed under argon gas atmosphere and carries out 500 ~ 800 DEG C of heat treatment 1 ~ 2h, after being cooled to room temperature, be immersed in hydrogen In fluoric acid, ultrasonic 10 ~ 15min is carried out with ultrasonic power 100 ~ 150w, remove surface local silicon dioxide, be centrifuged and be dried, obtain Antibacterial powder；

(5), under nitrogen environment, by concentration be the protonic acid solution of 0.05 ~ 0.5mol/l and concentration is the ten of 0.05 ~ 0.5mol/l Dialkyl benzene sulfonic acids are mixed with volume ratio 2 ~ 4:2, are simultaneously introduced the antibacterial powder that step (4) is obtained, after magnetic agitation 60 ~ 120min Add aniline, antibacterial powder and aniline mass ratio are 2:12 ~ 18；After continuously stirred 60 ~ 90min, dropwise Deca Ammonium persulfate., aniline It is 1:1 with Ammonium persulfate. mol ratio；15 ~ 30h is reacted at 20 DEG C～30 DEG C；Acetone, deionized water wash are vacuum dried for several times afterwards, Mill to obtain nano polyaniline/antibacterial flour complexes；

(6) prepare TiO 2 sol with sol-gel process, add the nanometer polyphenyl accounting for colloidal sol 0.01 ~ 1.0wt% in colloidal sol Amine/antibacterial flour complexes, mix homogeneously；60 DEG C～120 DEG C drying of the rearmounted baking oven of still aging 3～5d；After milling, gained is multiple Calcine 1 ~ 2h at 400～550 DEG C of compound, remove polyaniline, obtain poriferous titanium dioxide/antibacterial flour complexes；

(7) will be fully mixed to 30 ~ 45% epoxy resin, 35 ~ 50% phenolic resin and 8 ~ 20% poriferous titanium dioxides/antibacterial flour complexes Close, add appropriate butyl acetate to put into dispersion dispergation in ball mill, after discharge, detection, adjustment are configured to the slurry that can apply Material；By this slurry coating on substrate, drying and forming-film；Then it is placed in nitrogen filled protection atmosphere furnace, is warmed up to 900 ~ 1000 DEG C, protect Warm 1 ~ 2h；Film is scraped off this substrate, obtains antibiotic complex.

It is preferred that increasing by a step between step (4) and (5): take three-dimensional sponge shape Graphene ultrasonic agitation to be scattered in In aqueous solution, it is added dropwise over gqds/ag₂o/ag-zn-ce/sio₂In aqueous solution, three-dimensional sponge shape Graphene and gqds/ag₂o/ ag-zn-ce/sio₂Weight than for 1:1 ~ 5；Ultrasonic 60 ~ the 120min of 10 ~ 100w, standing, deionized water wash for several times, is dried Obtain gqds/ag₂o/ag-zn-ce/sio₂/ Graphene antibiosis powder.

In the present invention, described antibiotic complex can also be obtained by the following method:

(3) take 1 ~ 3ggqds/ag₂O ultrasonic agitation is scattered in aqueous solution；Being added dropwise over concentration is 0.05 ~ 0.5g/100mlzno Quantum dot aqueous solution, ultrasonic power mixing speed respectively halves；After 60 ~ 90min, standing, filter, be washed with deionized for several times, Vacuum drying, obtains gqds/ag₂O/zno antibacterial powder；

(4), under nitrogen environment, by concentration be the protonic acid solution of 0.05 ~ 0.5mol/l and concentration is the ten of 0.05 ~ 0.5mol/l Dialkyl benzene sulfonic acids are mixed with volume ratio 2 ~ 4:2, are simultaneously introduced the antibacterial powder that step (4) is obtained, after magnetic agitation 60 ~ 120min Add aniline, antibacterial powder and aniline mass ratio are 2:12 ~ 18；After continuously stirred 60 ~ 90min, dropwise Deca Ammonium persulfate., aniline It is 1:1 with Ammonium persulfate. mol ratio；15 ~ 30h is reacted at 20 DEG C～30 DEG C；Acetone, deionized water wash are vacuum dried for several times afterwards, Mill to obtain nano polyaniline/antibacterial flour complexes；

(5) prepare TiO 2 sol with sol-gel process, add the nanometer polyphenyl accounting for colloidal sol 0.01 ~ 1.0wt% in colloidal sol Amine/antibacterial flour complexes, mix homogeneously；60 DEG C～120 DEG C drying of the rearmounted baking oven of still aging 3～5d；After milling, gained is multiple Calcine 1 ~ 2h at 400～550 DEG C of compound, remove polyaniline, obtain poriferous titanium dioxide/antibacterial flour complexes；

(6) will be fully mixed to 30 ~ 45% epoxy resin, 35 ~ 50% phenolic resin and 8 ~ 20% poriferous titanium dioxides/antibacterial flour complexes Close, add appropriate butyl acetate to put into dispersion dispergation in ball mill, after discharge, detection, adjustment are configured to the slurry that can apply Material；By this slurry coating on substrate, drying and forming-film；Then it is placed in nitrogen filled protection atmosphere furnace, is warmed up to 900 ~ 1000 DEG C, protect Warm 1 ~ 2h；Film is scraped off this substrate, obtains antibiotic complex.

It is preferred that increasing by a step between step (3) and (4): take three-dimensional sponge shape Graphene ultrasonic agitation to be scattered in In aqueous solution, it is added dropwise over gqds/ag₂In o/zno aqueous solution, three-dimensional sponge shape Graphene and gqds/ag₂The weight ratio of o/zno For 1:1 ~ 5；Ultrasonic 60 ~ the 120min of 10 ~ 100w, standing, deionized water wash for several times, dry gqds/ag₂O/zno/ Graphene Antibacterial powder.

The invention has the following beneficial effects: this method loads and fixing antibacterial in carbon nano net, not only prevent it Reunite, significantly improve the stability of the antibacterial such as metal nanoparticle so as to can more preferably be dispersed in glaze modelled after an antique, and have longer The antibacterial activity of effect and silver ion will not overflow oxidation stain；It is compounded with the anti-microbial property of multiple antibacterial simultaneously, compared to Single silver nano antibacterial agent has more preferable antibacterial effect, and antibacterial is lasting；Anion complex can efficiently continual release Anion, equal energy uninterruptedly anion releasing, effective purify air, organic gas such as decomposing formaldehyde under having light or no light condition Body, improves IAQ (indoor air quality), also has the effect of antibacterial, be beneficial to health.Compare with existing glaze modelled after an antique, system of the present invention The glaze dispensing science modelled after an antique made, rationally, colour generation is pure, stable performance for preparation；Simultaneously through rational anion complex of arranging in pairs or groups And antimicrobial composite material, excellent antibacterial is antifouling and purify air characteristic so that glaze modelled after an antique has for both synergism, opens up further The wide range of application of glaze modelled after an antique.

Specific embodiment

To further illustrate technical scheme below by specific preferred implementation.

Embodiment 1

Step a, prepares anion low temperature frit: by 10% quartz, 10% Anhydrite, 16% Borax, 12% carbonate, 35% boric acid, 3% lithium Pyroxene, 4% fluoride salt, 1.5% Kaolin mixed grinding are uniform；Add 0.5% antibiotic complex and 8% anion complex, grind Mill is uniformly obtained compound；Compound is dispensed in loading fire resistant sagger, carries out 1250 ~ 1320 DEG C of high temperature meltings, melted The slurry of state；By slurry water quenching cooling, and it is broken into graininess, prepared anion low temperature frit；Wherein, described Anhydrite is long by potassium Stone and albite are obtained by mixing by weight 4:1；Described carbonate is by potassium carbonate, sodium carbonate, brium carbonate, lithium carbonate and Calcium Carbonate It is obtained by mixing by weight 3:1:3:2:1；Described fluoride salt is mixed by weight 4:2:1 by sodium fluoride, calcium fluoride and lithium fluoride And obtain；

Step b, prepares glaze slip: by mass percentage, by 32% low temperature frit, 8% coloring agent, 32% potassium feldspar, 10% stone English, 4% calcite, 5% Talcum, 5% calcium phosphate, 3% antibiotic complex and 1% anion complex are mixed to get mixed powder End, adds sodium tripolyphosphate and carboxymethyl cellulose mix homogeneously in mixed-powder, is finely ground to 300 ~ 350 mesh, Ran Houjia Enter water to obtain glaze slip and modulate glaze slip proportion for 1.6 ~ 1.7g/cm³；Wherein, the addition of sodium tripolyphosphate is mixed-powder quality 0.3%, the addition of carboxymethyl cellulose is the 2% of mixed-powder quality；Described coloring agent is less than 200 purposes for particle diameter and surpasses Thin slag, its preparation process is as follows: Iron-ore Slag is roughly ground to can grind uniform in mortar, then enter by 60 ~ 80 mesh sieves after Row ball milling, drum's speed of rotation is 1500r/min, and Ball-milling Time is 60min；Then 200 ~ 250 mesh sieves, prepared ultrafine slag are crossed；

Wherein, described anion complex preparation method is as follows: by 10% coral fossil, 10% tourmaline, 35% opal, 1% serpentine, 10% Maifanitum, 5% rare ice stone, 1% hokutolite, 5% Doctor king stone, 5% shell, 10% kieselguhr, 1% iron sesquioxide, 3% aluminium sesquioxide, 3% zirconium oxide and 1% zirconium phosphate mix homogeneously, add in grinding equipment and carry out superfine grinding, until granule is straight Footpath is distributed in 50 ~ 80nm, sieves, and is dried, you can described anion powder is obtained.8g anion powder is taken to be scattered in 120ml ultra-pure water In, water bath sonicator 2h obtains all even stable dispersion liquid；When the substrate with carbon nanotube mesh film is placed in about 8 DEG C, will Dispersion liquid adds in the substrate of concave shape, meanwhile, rolls around roller, makes this homogeneous dispersion be scattered in this carbon nano-tube network In shape film, due to when CNT is near 8 DEG C, there is hydrophilic, this dispersion liquid is attracted to the multiple of carbon nanotube mesh film Net hole；It is warming up to about 25 DEG C, CNT has hydrophobicity drive hydrone away and leaves behind anion powder and adsorbs in carbon nanometer In multiple net holes of pipe reticular membrane；After drying, the carbon nanotube mesh film being adsorbed with anion powder is scraped off this substrate, obtain negative Ion powder/CNT.

Wherein, described antibiotic complex is obtained by the following method:

(1) weigh 0.6gc60 powder, measure the concentrated sulphuric acid that 100ml mass fraction is 98%, c60 powder and concentrated sulphuric acid are being burnt Mix in cup, beaker is placed in ice-water bath, stirred with the speed of 600rpm simultaneously, obtain mixed liquor；Weigh 1g potassium permanganate powder, Slowly add in above-mentioned mixed liquor；Remove ice-water bath, change water-bath into, keep 30 ~ 40 DEG C of bath temperature, react 4h；Quickly add Enter 120ml pure water, filter, then dialysed 4 days with the bag filter that molecular cut off is 1000, obtain graphene quantum dot (gqds) and hang Supernatant liquid；100rpm speed stirs gqds suspension, laser irradiation 40min simultaneously, and laser irradiation power is 1w；Standby；

(2) ultrasonic agitation 60mlgqds suspension, Deca concentration is 0.001mol/l silver nitrate aqueous solution；Being added dropwise over concentration is 0.1mol/l ammonium dihydrogen phosphate (ammonium dihydrogen phosphate and silver nitrate aqueous solution volume ratio are 2:1), ultrasonic agitation 20min；It is added dropwise over 1mol/l sodium hydroxide solution, regulation ph value to 11, then standing, centrifugation, deionized water and ethanol Alternately washing three times, vacuum drying, obtain gqds/ag₂o；

(3) take 1ggqds/ag₂O ultrasonic agitation is scattered in 100ml aqueous solution；Being added dropwise over concentration is 0.05mol/l cerous nitrate Aqueous solution, being added dropwise over concentration after 30min is 0.005mol/l zinc nitrate aqueous solution, gqds/ag₂O aqueous solution, cerous nitrate are water-soluble Liquid and zinc nitrate aqueous solution volume ratio are 1:0.1:0.4；Continue ultrasonic agitation, regulation mixed solution ph value to 7.0；Side is ultrasonic to be stirred Mix, side adds the hydrazine hydrate that 6ml mass fraction is 50%, reduction reaction 0.5h at 30 DEG C；Afterwards, add 45ml mass to divide The hydrazine hydrate for 50% for the number, after reduction reaction 36h at 85 DEG C；Filter, be washed with deionized for several times, vacuum drying, obtain gqds/ag₂o/ag-zn-ce；

(4) by 0.5ggqds/ag₂O/ag-zn-ce ultrasonic agitation is scattered in aqueous solution；Afterwards add volume ratio 4:1 water and Ammonia, is stirring evenly and then adding into tetraethyl orthosilicate (with gqds/ag₂The mass ratio of o/ag-zn-ce is 3:2), adjust ph value for 9 ~ 10, reaction temperature is 20 ~ 25 DEG C, reacts 30min；Carry out centrifugation and clean acquisition precipitation successively with acetone and deionized water；Will This is deposited in and 3h is dried at 90 DEG C, to obtain gqds/ag₂o/ag-zn-ce/sio₂；By gqds/ag₂o/ag-zn-ce/sio₂Put Carry out 600 DEG C of heat treatment 1h under argon gas atmosphere, after being cooled to room temperature, be immersed in Fluohydric acid. and surpassed with ultrasonic power 100w Sound 10min, removes surface local silicon dioxide, is centrifuged and is dried, obtains antibacterial powder；

(5) under nitrogen environment, by the detergent alkylate sulphur for 0.1mol/l for the protonic acid solution and concentration for 0.2mol/l for the concentration Acid, with the mixing of volume ratio 3:2, is simultaneously introduced the antibacterial powder that step (4) is obtained, and adds aniline, antibacterial powder after magnetic agitation 100min After being the continuously stirred 90min of 2:18 with aniline mass ratio, dropwise Deca Ammonium persulfate., aniline and Ammonium persulfate. mol ratio are 1:1； 20h is reacted at 20 DEG C～30 DEG C；Acetone, deionized water wash are vacuum dried for several times afterwards, mill nano polyaniline/antibacterial powder is multiple Compound；

(6) prepare TiO 2 sol with sol-gel process, add in colloidal sol and account for the nano polyaniline of colloidal sol 1.0wt%/anti- Mycopowder complex, mix homogeneously；The 90 DEG C of drying of the rearmounted baking oven of still aging 4d；To calcine at 500 DEG C of gained complex after milling 1h, removes polyaniline, obtains poriferous titanium dioxide/antibacterial flour complexes；

(7) 30% epoxy resin, 50% phenolic resin and 20% poriferous titanium dioxide/antibacterial flour complexes are sufficiently mixed, add suitable The butyl acetate of amount puts into dispersion dispergation in ball mill, and after discharge, detection, adjustment are configured to the slurry that can apply；This is starched Material is coated on substrate, drying and forming-film；Then it is placed in nitrogen filled protection atmosphere furnace, is warmed up to 900 DEG C, be incubated 1.5h；Film is scraped From this substrate, obtain antibiotic complex.

Embodiment 2

Step a, prepares anion low temperature frit: by 15% quartz, 8% Anhydrite, 25% Borax, 8% carbonate, 27% boric acid, 5% lithium brightness Stone, 3% fluoride salt, 3% Kaolin mixed grinding are uniform；Add 1% antibiotic complex and 5% anion complex, grind uniformly Prepared compound；Compound is dispensed in loading fire resistant sagger, carries out 1250 ~ 1320 DEG C of high temperature meltings, obtain the slurry of molten state Material；By slurry water quenching cooling, and it is broken into graininess, prepared anion low temperature frit；Wherein, described Anhydrite is by potassium feldspar and sodium Anhydrite is obtained by mixing by weight 4:1；Described carbonate is by potassium carbonate, sodium carbonate, brium carbonate, lithium carbonate and Calcium Carbonate by weight It is obtained by mixing than 3:1:3:2:1；Described fluoride salt is obtained by mixing by weight 4:2:1 by sodium fluoride, calcium fluoride and lithium fluoride；

Step b, prepares glaze slip: by mass percentage, by 25% low temperature frit, 5% coloring agent, 29% potassium feldspar, 20% stone English, 5% calcite, 5% Talcum, 4% calcium phosphate, 2% antibiotic complex and 5% anion complex are mixed to get mixed powder End, adds sodium tripolyphosphate and carboxymethyl cellulose mix homogeneously in mixed-powder, is finely ground to 300 ~ 350 mesh, Ran Houjia Enter water to obtain glaze slip and modulate glaze slip proportion for 1.6 ~ 1.7g/cm³；Wherein, the addition of sodium tripolyphosphate is mixed-powder quality 0.3%, the addition of carboxymethyl cellulose is the 2% of mixed-powder quality；Described coloring agent is less than 200 purposes for particle diameter and surpasses Thin slag, its preparation process is as follows: Iron-ore Slag is roughly ground to can grind uniform in mortar, then enter by 60 ~ 80 mesh sieves after Row ball milling, drum's speed of rotation is 1500r/min, and Ball-milling Time is 60min；Then 200 ~ 250 mesh sieves, prepared ultrafine slag are crossed；

Wherein, described anion complex preparation method is as follows: by 8% coral fossil, 12% tourmaline, 25% opal, 3% Serpentine, 8% Maifanitum, 3% rare ice stone, 3% hokutolite, 3% Doctor king stone, 8% shell, 12% kieselguhr, 2% iron sesquioxide, 5% 3 Al 2 O, 6% zirconium oxide and 2% zirconium phosphate mix homogeneously, add in grinding equipment and carry out superfine grinding, until particle diameter divides Cloth, in 50 ~ 80nm, sieves, and is dried, you can described anion powder is obtained.8g anion powder is taken to be scattered in 120ml ultra-pure water, water Bathe ultrasonic 2h and obtain all even stable dispersion liquid；When the substrate with carbon nanotube mesh film is placed in about 8 DEG C, by dispersion liquid Add in the substrate of concave shape, meanwhile, roll around roller, make this homogeneous dispersion be scattered in this carbon nanotube mesh film In, due to when CNT is near 8 DEG C, there is hydrophilic, this dispersion liquid is attracted to multiple nets of carbon nanotube mesh film Hole；It is warming up to about 25 DEG C, CNT has hydrophobicity drive hydrone away and leaves behind anion powder and adsorbs in CNT In multiple net holes of reticular membrane；After drying, the carbon nanotube mesh film being adsorbed with anion powder is scraped off this substrate, obtain bear from Sub- powder/CNT.

Wherein, described antibiotic complex is obtained by the following method:

(2) ultrasonic agitation 60mlgqds suspension, Deca concentration is 0.005mol/l silver nitrate aqueous solution；Being added dropwise over concentration is 0.2mol/l ammonium dihydrogen phosphate (ammonium dihydrogen phosphate and silver nitrate aqueous solution volume ratio are 2:1), ultrasonic agitation 20min；It is added dropwise over 1mol/l sodium hydroxide solution, regulation ph value to 11, then standing, centrifugation, deionized water and ethanol Alternately washing three times, vacuum drying, obtain gqds/ag₂o；

(3) take 2ggqds/ag₂O ultrasonic agitation is scattered in 100ml aqueous solution；Being added dropwise over concentration is 0.03mol/l cerous nitrate Aqueous solution, being added dropwise over concentration after 30min is 0.03mol/l zinc nitrate aqueous solution, gqds/ag₂O aqueous solution, cerous nitrate are water-soluble Liquid and zinc nitrate aqueous solution volume ratio are 1:0.2:0.3；Continue ultrasonic agitation, regulation mixed solution ph value to 7.0；Side is ultrasonic to be stirred Mix, side adds the hydrazine hydrate that 6ml mass fraction is 50%, reduction reaction 0.5h at 30 DEG C；Afterwards, add 45ml mass to divide The hydrazine hydrate for 50% for the number, after reduction reaction 36h at 85 DEG C；Filter, be washed with deionized for several times, vacuum drying, obtain gqds/ag₂o/ag-zn-ce；

(4) by 0.3ggqds/ag₂O/ag-zn-ce ultrasonic agitation is scattered in aqueous solution；Afterwards add volume ratio 4:1 water and Ammonia, is stirring evenly and then adding into tetraethyl orthosilicate (with gqds/ag₂The mass ratio of o/ag-zn-ce is 3:2), adjust ph value for 9 ~ 10, reaction temperature is 20 ~ 25 DEG C, reacts 45min；Carry out centrifugation and clean acquisition precipitation successively with acetone and deionized water；Will This is deposited in and 3h is dried at 90 DEG C, to obtain gqds/ag₂o/ag-zn-ce/sio₂；By gqds/ag₂o/ag-zn-ce/sio₂Put Carry out 600 DEG C of heat treatment 1h under argon gas atmosphere, after being cooled to room temperature, be immersed in Fluohydric acid. and surpassed with ultrasonic power 100w Sound 12min, removes surface local silicon dioxide, is centrifuged and is dried, obtains antibacterial powder；

(5) under nitrogen environment, by the detergent alkylate sulphur for 0.1mol/l for the protonic acid solution and concentration for 0.2mol/l for the concentration Acid, with the mixing of volume ratio 3:2, is simultaneously introduced the antibacterial powder that step (4) is obtained, and adds aniline, antibacterial powder after magnetic agitation 100min After being the continuously stirred 90min of 2:15 with aniline mass ratio, dropwise Deca Ammonium persulfate., aniline and Ammonium persulfate. mol ratio are 1:1； 20h is reacted at 20 DEG C～30 DEG C；Acetone, deionized water wash are vacuum dried for several times afterwards, mill nano polyaniline/antibacterial powder is multiple Compound；

(6) prepare TiO 2 sol with sol-gel process, add in colloidal sol and account for the nano polyaniline of colloidal sol 0.5wt%/anti- Mycopowder complex, mix homogeneously；The 90 DEG C of drying of the rearmounted baking oven of still aging 4d；To calcine at 500 DEG C of gained complex after milling 1h, removes polyaniline, obtains poriferous titanium dioxide/antibacterial flour complexes；

(7) 45% epoxy resin, 35% phenolic resin and 20% poriferous titanium dioxide/antibacterial flour complexes are sufficiently mixed, add suitable The butyl acetate of amount puts into dispersion dispergation in ball mill, and after discharge, detection, adjustment are configured to the slurry that can apply；This is starched Material is coated on substrate, drying and forming-film；Then it is placed in nitrogen filled protection atmosphere furnace, is warmed up to 900 DEG C, be incubated 1.5h；Film is scraped From this substrate, obtain antibiotic complex.

Embodiment 3

Step a, prepares anion low temperature frit: by 18% quartz, 12% Anhydrite, 21% Borax, 5% carbonate, 27% boric acid, 8% lithium Pyroxene, 1% fluoride salt, 5% Kaolin mixed grinding are uniform；Add 2% antibiotic complex and 1% anion complex, grind all Even prepared compound；Compound is dispensed in loading fire resistant sagger, carries out 1250 ~ 1320 DEG C of high temperature meltings, obtain molten state Slurry；By slurry water quenching cooling, and it is broken into graininess, prepared anion low temperature frit；Wherein, described Anhydrite by potassium feldspar and Albite is obtained by mixing by weight 4:1；Described carbonate presses weight by potassium carbonate, sodium carbonate, brium carbonate, lithium carbonate and Calcium Carbonate Amount is obtained by mixing than 3:1:3:2:1；Described fluoride salt is obtained by mixing by weight 4:2:1 by sodium fluoride, calcium fluoride and lithium fluoride；

Step b, prepares glaze slip: by mass percentage, by 27% low temperature frit, 3% coloring agent, 38% potassium feldspar, 13% stone English, 5% calcite, 3% Talcum, 2% calcium phosphate, 1% antibiotic complex and 8% anion complex are mixed to get mixed powder End, adds sodium tripolyphosphate and carboxymethyl cellulose mix homogeneously in mixed-powder, is finely ground to 300 ~ 350 mesh, Ran Houjia Enter water to obtain glaze slip and modulate glaze slip proportion for 1.6 ~ 1.7g/cm³；Wherein, the addition of sodium tripolyphosphate is mixed-powder quality 0.3%, the addition of carboxymethyl cellulose is the 2% of mixed-powder quality；Described coloring agent is less than 200 purposes for particle diameter and surpasses Thin slag, its preparation process is as follows: Iron-ore Slag is roughly ground to can grind uniform in mortar, then enter by 60 ~ 80 mesh sieves after Row ball milling, drum's speed of rotation is 1500r/min, and Ball-milling Time is 60min；Then 200 ~ 250 mesh sieves, prepared ultrafine slag are crossed；

Wherein, described anion complex preparation method is as follows: by 5% coral fossil, 15% tourmaline, 20% opal, 5% Serpentine, 5% Maifanitum, 1% rare ice stone, 5% hokutolite, 1% Doctor king stone, 10% shell, 15% kieselguhr, 3% iron sesquioxide, 2% Aluminium sesquioxide, 8% zirconium oxide and 5% zirconium phosphate mix homogeneously, add in grinding equipment and carry out superfine grinding, until particle diameter It is distributed in 50 ~ 80nm, sieves, be dried, you can described anion powder is obtained.8g anion powder is taken to be scattered in 120ml ultra-pure water, Water bath sonicator 2h obtains all even stable dispersion liquid；When the substrate with carbon nanotube mesh film is placed in about 8 DEG C, will disperse Liquid adds in the substrate of concave shape, meanwhile, rolls around roller, makes this homogeneous dispersion be scattered in this carbon nanotube mesh film In, due to when CNT is near 8 DEG C, there is hydrophilic, this dispersion liquid is attracted to multiple nets of carbon nanotube mesh film Hole；It is warming up to about 25 DEG C, CNT has hydrophobicity drive hydrone away and leaves behind anion powder and adsorbs in CNT In multiple net holes of reticular membrane；After drying, the carbon nanotube mesh film being adsorbed with anion powder is scraped off this substrate, obtain bear from Sub- powder/CNT.

Wherein, antibiotic complex is obtained by the following method:

(2) ultrasonic agitation 60mlgqds suspension, Deca concentration is 0.01mol/l silver nitrate aqueous solution；Being added dropwise over concentration is 0.5mol/l ammonium dihydrogen phosphate (ammonium dihydrogen phosphate and silver nitrate aqueous solution volume ratio are 2:1), ultrasonic agitation 20min；It is added dropwise over 1mol/l sodium hydroxide solution, regulation ph value to 11, then standing, centrifugation, deionized water and ethanol Alternately washing three times, vacuum drying, obtain gqds/ag₂o；

(3) take 3ggqds/ag₂O ultrasonic agitation is scattered in 100ml aqueous solution；Being added dropwise over concentration is 0.005mol/l nitric acid Cerium aqueous solution, being added dropwise over concentration after 30min is 0.05mol/l zinc nitrate aqueous solution, gqds/ag₂O aqueous solution, cerous nitrate water Solution and zinc nitrate aqueous solution volume ratio are 1:0.2:0.4；Continue ultrasonic agitation, regulation mixed solution ph value to 7.0；Side is ultrasonic Stirring, side adds the hydrazine hydrate that 6ml mass fraction is 50%, reduction reaction 0.5h at 30 DEG C；Afterwards, add 45ml mass Fraction is 50% hydrazine hydrate, after reduction reaction 36h at 85 DEG C；Filter, be washed with deionized for several times, vacuum drying, obtain gqds/ag₂o/ag-zn-ce；

(4) by 0.1ggqds/ag₂O/ag-zn-ce ultrasonic agitation is scattered in aqueous solution；Afterwards add volume ratio 4:1 water and Ammonia, is stirring evenly and then adding into tetraethyl orthosilicate (with gqds/ag₂The mass ratio of o/ag-zn-ce is 3:2), adjust ph value for 9 ~ 10, reaction temperature is 20 ~ 25 DEG C, reacts 60min；Carry out centrifugation and clean acquisition precipitation successively with acetone and deionized water；Will This is deposited in and 3h is dried at 90 DEG C, to obtain gqds/ag₂o/ag-zn-ce/sio₂；By gqds/ag₂o/ag-zn-ce/sio₂Put Carry out 600 DEG C of heat treatment 1h under argon gas atmosphere, after being cooled to room temperature, be immersed in Fluohydric acid. and surpassed with ultrasonic power 100w Sound 15min, removes surface local silicon dioxide, is centrifuged and is dried, obtains antibacterial powder；

(5) under nitrogen environment, by the detergent alkylate sulphur for 0.1mol/l for the protonic acid solution and concentration for 0.2mol/l for the concentration Acid, with the mixing of volume ratio 3:2, is simultaneously introduced the antibacterial powder that step (4) is obtained, and adds aniline, antibacterial powder after magnetic agitation 100min After being the continuously stirred 90min of 2:12 with aniline mass ratio, dropwise Deca Ammonium persulfate., aniline and Ammonium persulfate. mol ratio are 1:1； 20h is reacted at 20 DEG C～30 DEG C；Acetone, deionized water wash are vacuum dried for several times afterwards, mill nano polyaniline/antibacterial powder is multiple Compound；

(6) prepare TiO 2 sol with sol-gel process, add in colloidal sol account for the nano polyaniline of colloidal sol 0.01wt%/ Antibacterial flour complexes, mix homogeneously；The 90 DEG C of drying of the rearmounted baking oven of still aging 4d；Forge at 500 DEG C of gained complex after milling Burn 1h, remove polyaniline, obtain poriferous titanium dioxide/antibacterial flour complexes；

(7) 40% epoxy resin, 40% phenolic resin and 20% poriferous titanium dioxide/antibacterial flour complexes are sufficiently mixed, add suitable The butyl acetate of amount puts into dispersion dispergation in ball mill, and after discharge, detection, adjustment are configured to the slurry that can apply；This is starched Material is coated on substrate, drying and forming-film；Then it is placed in nitrogen filled protection atmosphere furnace, is warmed up to 900 DEG C, be incubated 1.5h；Film is scraped From this substrate, obtain antibiotic complex.

Embodiment 4

Based on the preparation method of embodiment 2, difference is: increases following steps between step (4) and (5): take three-dimensional sea Continuous shape Graphene ultrasonic agitation is scattered in aqueous solution, is added dropwise over gqds/ag₂o/ag-zn-ce/sio₂In aqueous solution, three-dimensional Spongy graphene and gqds/ag₂o/ag-zn-ce/sio₂Weight than for 1:3；The ultrasonic 90min of 50w, standing, deionized water Washing for several times, dry gqds/ag₂o/ag-zn-ce/sio₂/ Graphene antibiosis powder.

Three-dimensional sponge shape graphene preparation method is as follows: by 3g graphite powder, 1g nano3 in ice-water bath with 250ml 98% concentrated sulphuric acid mix homogeneously, is slowly added to 6g kmno4.Then heat at 35 DEG C, after stirring 40min, add 95ml to go Ionized water, is warming up to 98 DEG C of reaction 20min；Add 270ml water dilution, and with 5ml 30% h2o2 with unnecessary kmno4, The color of mixed solution is brown color, filtered while hot, and deionized water cyclic washing obtains go to neutrality, ultrasonic disperse；Take 200ml mass fraction is that the graphene oxide solution of 5mg/ml pours diameter 25cm into, in the discoid reaction utensil of high 2cm, adds Ascorbic acid (vc) 0.5g stirring makes it be sufficiently mixed；Then confined reaction ware is placed in 80 DEG C of hydro-thermal reactions 15h, in reaction utensil Graphene oxide Spontaneous Contraction be cross-linked into three-dimensional sponge structure, lyophilization, obtain flexibility three-dimensional sponge shape Graphene.

Embodiment 5

Based on the preparation method of embodiment 1, difference is: described antibiotic complex is obtained by the following method:

(3) take 1ggqds/ag₂O ultrasonic agitation is scattered in aqueous solution；Being added dropwise over concentration is 0.5g/100mlzno quantum dot Aqueous solution, ultrasonic power mixing speed respectively halves；After 60min, standing, filter, be washed with deionized for several times, vacuum drying, Obtain gqds/ag₂O/zno antibacterial powder；

(4) under nitrogen environment, by the detergent alkylate sulphur for 0.1mol/l for the protonic acid solution and concentration for 0.2mol/l for the concentration Acid, with the mixing of volume ratio 3:2, is simultaneously introduced the antibacterial powder that step (4) is obtained, and adds aniline, antibacterial powder after magnetic agitation 100min After being the continuously stirred 90min of 2:18 with aniline mass ratio, dropwise Deca Ammonium persulfate., aniline and Ammonium persulfate. mol ratio are 1:1； 20h is reacted at 20 DEG C～30 DEG C；Acetone, deionized water wash are vacuum dried for several times afterwards, mill nano polyaniline/antibacterial powder is multiple Compound；

(5) prepare TiO 2 sol with sol-gel process, add in colloidal sol and account for the nano polyaniline of colloidal sol 1.0wt%/anti- Mycopowder complex, mix homogeneously；The 90 DEG C of drying of the rearmounted baking oven of still aging 4d；To calcine at 500 DEG C of gained complex after milling 1h, removes polyaniline, obtains poriferous titanium dioxide/antibacterial flour complexes；

(6) 30% epoxy resin, 50% phenolic resin and 20% poriferous titanium dioxide/antibacterial flour complexes are sufficiently mixed, add suitable The butyl acetate of amount puts into dispersion dispergation in ball mill, and after discharge, detection, adjustment are configured to the slurry that can apply；This is starched Material is coated on substrate, drying and forming-film；Then it is placed in nitrogen filled protection atmosphere furnace, is warmed up to 900 DEG C, be incubated 1.5h；Film is scraped From this substrate, obtain antibiotic complex.

Embodiment 6

Based on the preparation method of embodiment 2, difference is: described antibiotic complex is obtained by the following method:

(3) take 2ggqds/ag₂O ultrasonic agitation is scattered in aqueous solution；Being added dropwise over concentration is 0.2g/100mlzno quantum dot Aqueous solution, ultrasonic power mixing speed respectively halves；After 80min, standing, filter, be washed with deionized for several times, vacuum drying, Obtain gqds/ag₂O/zno antibacterial powder；

(4) under nitrogen environment, by the detergent alkylate sulphur for 0.1mol/l for the protonic acid solution and concentration for 0.2mol/l for the concentration Acid, with the mixing of volume ratio 3:2, is simultaneously introduced the antibacterial powder that step (4) is obtained, and adds aniline, antibacterial powder after magnetic agitation 100min After being the continuously stirred 90min of 2:15 with aniline mass ratio, dropwise Deca Ammonium persulfate., aniline and Ammonium persulfate. mol ratio are 1:1； 20h is reacted at 20 DEG C～30 DEG C；Acetone, deionized water wash are vacuum dried for several times afterwards, mill nano polyaniline/antibacterial powder is multiple Compound；

(5) prepare TiO 2 sol with sol-gel process, add in colloidal sol and account for the nano polyaniline of colloidal sol 0.5wt%/anti- Mycopowder complex, mix homogeneously；The 90 DEG C of drying of the rearmounted baking oven of still aging 4d；To calcine at 500 DEG C of gained complex after milling 1h, removes polyaniline, obtains poriferous titanium dioxide/antibacterial flour complexes；

(6) 45% epoxy resin, 35% phenolic resin and 20% poriferous titanium dioxide/antibacterial flour complexes are sufficiently mixed, add suitable The butyl acetate of amount puts into dispersion dispergation in ball mill, and after discharge, detection, adjustment are configured to the slurry that can apply；This is starched Material is coated on substrate, drying and forming-film；Then it is placed in nitrogen filled protection atmosphere furnace, is warmed up to 900 DEG C, be incubated 1.5h；Film is scraped From this substrate, obtain antibiotic complex.

Embodiment 7

Based on the preparation method of embodiment 3, difference is: described antibiotic complex is obtained by the following method:

(3) take 3ggqds/ag₂O ultrasonic agitation is scattered in aqueous solution；Being added dropwise over concentration is 0.05g/100mlzno quantum dot Aqueous solution, ultrasonic power mixing speed respectively halves；After 90min, standing, filter, be washed with deionized for several times, vacuum drying, Obtain gqds/ag₂O/zno antibacterial powder；

(4) under nitrogen environment, by the detergent alkylate sulphur for 0.1mol/l for the protonic acid solution and concentration for 0.2mol/l for the concentration Acid, with the mixing of volume ratio 3:2, is simultaneously introduced the antibacterial powder that step (4) is obtained, and adds aniline, antibacterial powder after magnetic agitation 100min After being the continuously stirred 90min of 2:12 with aniline mass ratio, dropwise Deca Ammonium persulfate., aniline and Ammonium persulfate. mol ratio are 1:1； 20h is reacted at 20 DEG C～30 DEG C；Acetone, deionized water wash are vacuum dried for several times afterwards, mill nano polyaniline/antibacterial powder is multiple Compound；

(5) prepare TiO 2 sol with sol-gel process, add in colloidal sol account for the nano polyaniline of colloidal sol 0.01wt%/ Antibacterial flour complexes, mix homogeneously；The 90 DEG C of drying of the rearmounted baking oven of still aging 4d；Forge at 500 DEG C of gained complex after milling Burn 1h, remove polyaniline, obtain poriferous titanium dioxide/antibacterial flour complexes；

(6) 40% epoxy resin, 40% phenolic resin and 20% poriferous titanium dioxide/antibacterial flour complexes are sufficiently mixed, add suitable The butyl acetate of amount puts into dispersion dispergation in ball mill, and after discharge, detection, adjustment are configured to the slurry that can apply；This is starched Material is coated on substrate, drying and forming-film；Then it is placed in nitrogen filled protection atmosphere furnace, is warmed up to 900 DEG C, be incubated 1.5h；Film is scraped From this substrate, obtain antibiotic complex.

Embodiment 8

Based on the preparation method of embodiment 6, difference is: increases such as next step between step (3) and (4): take three-dimensional Spongy graphene ultrasonic agitation is scattered in aqueous solution, is added dropwise over gqds/ag₂In o/zno aqueous solution, three-dimensional sponge shape stone Black alkene and gqds/ag₂The weight of o/zno is than for 1:3；The ultrasonic 90min of 50w, standing, deionized water wash is for several times, dry gqds/ag₂O/zno/ Graphene antibiosis powder.

Comparative example 1

Based on the preparation method of embodiment 1, difference is: described antibiotic complex is the titanium dioxide carrying metal antibacterial agent Titanium；It is not added with anion complex.

Comparative example 2

Based on the preparation method of embodiment 5, difference is: described antibiotic complex is the mixing of zinc oxide and titanium dioxide Thing；Described anion complex is anion powder, by 8% coral fossil, 12% tourmaline, 25% opal, 4% serpentine, 7% wheat Meal stone, 4% rare ice stone, 4% hokutolite, 3% Doctor king stone, 8% shell, 12% kieselguhr, 2% iron sesquioxide, 3% aluminium sesquioxide, 5% Zirconium oxide and 3% zirconium phosphate mix homogeneously, add in grinding equipment and carry out superfine grinding, until particle diameter distribution 50 ~ 80nm, sieves, and is dried, you can described anion powder is obtained.

Embodiment 1 ~ 8 and comparative example 1,2 are carried out performance test, test result is as follows:

Sterilization rate: take 10⁵The escherichia coli 0.1ml of individual/ml, is spread evenly across on the 40*40mm burning till glaze modelled after an antique, indoors Place 2h, then bacterium solution sterilized water is eluted in culture medium, cultivate 24h at 37 DEG C, then detect bacterium number, calculate sterilizing Rate.

Heat stability is tested: finished product is placed in electric furnace, is raised to 200 DEG C from room temperature, be incubated 20min, put into 25 DEG C rapidly In water, take out after 10min and dry, glaze layer no temperature shock crackle simultaneously tests its sterilization rate.

Wear testing: the abrasive material being 3～4 from Mohs' hardness, friction to imitate paving 1000 times on by glaze modelled after an antique makes With the effect after 2 years.

Antifouling test: be pollutant from chrome green.

Sterilizing Evaluation for Uniformity: 100 regions are chosen on glaze modelled after an antique and carries out sterilizing test, the data recording is carried out all Evenness analysis, by the uniformity=100* (1- standard deviation/meansigma methodss).When the uniformity is more than 97%, then be labeled as ▲；When uniform Degree more than 90% and is less than 97%, then be labeled as ☆；When the uniformity is less than 90%, then it is labeled as.

Anion burst size: com-3010pro type ion detector test anion burst size is produced using Japan, by this sample Product are positioned over 1m³Test box (length is 1m) in, record in the air air-anion concentration (initial and 24h)；Adopt With the test of Han Wang m1 type haze table, pm2.5 concentration (1h and 24h) in test box；In test box, (formaldehyde is dense for Deca 0.1mg formaldehyde Degree 0.1mg/m³), record concentration of formaldehyde after 24h.

Embodiment described above only have expressed embodiments of the present invention, and its description is more concrete and detailed, but can not Therefore it is interpreted as the restriction to the scope of the claims of the present invention, as long as the skill being obtained in the form of equivalent or equivalent transformation Art scheme, all should fall within the scope and spirit of the invention.

Claims

1. a kind of preparation method of the low temperature glaze modelled after an antique with purify air effect, it comprises the following steps:

2. the preparation method of the low temperature glaze modelled after an antique with purify air effect according to claim 1 is it is characterised in that institute The preparation method stating antibiotic complex is as follows:

(1) weigh 0.3 ~ 1gc60 powder, measure the concentrated sulphuric acid that 80 ~ 100ml mass fraction is 98%, by c60 powder and concentrated sulphuric acid Beaker mixes, beaker is placed in ice-water bath, stirred with the speed of 500 ~ 600rpm simultaneously, obtain mixed liquor；Weigh 1 ~ 3g high Potassium manganate powder, slowly adds in above-mentioned mixed liquor；Remove ice-water bath, change water-bath into, keep 30 ~ 40 DEG C of bath temperature, instead Answer 3 ~ 5h；Rapidly join 100 ~ 150ml pure water, filter, then dialysed 3 ~ 5 days with the bag filter that molecular cut off is 1000, obtain Gqds suspension；100 ~ 150rpm speed stirs gqds suspension, laser irradiation 30 ~ 60min simultaneously, and laser irradiation power is 0.5~2w；Standby；

(2) ultrasonic agitation 50 ~ 60mlgqds suspension, Deca concentration is 0.001 ~ 0.01mol/l silver nitrate aqueous solution；Dropwise plus Entering concentration is 0.1 ~ 0.5mol/l ammonium dihydrogen phosphate, ultrasonic agitation 10 ~ 20min；It is added dropwise over 0.5 ~ 1mol/l hydroxide Sodium solution, adjusts ph value to 11, then stands, is centrifuged, deionized water and ethanol replace washing three times, vacuum drying, obtain gqds/ag₂o；

(4) by 0.1 ~ 0.5ggqds/ag₂O/ag-zn-ce ultrasonic agitation is scattered in aqueous solution；Add volume ratio 3 ~ 5:1 afterwards Water and ammonia, be stirring evenly and then adding into, adjust ph value be 9 ~ 10, reaction temperature be 20 ~ 25 DEG C, react 30 ~ 60min；Carry out Centrifugation simultaneously cleans acquisition precipitation successively with acetone and deionized water；This is deposited at 80 ~ 90 DEG C 2 ~ 4h is dried, to obtain gqds/ag₂o/ag-zn-ce/sio₂；By gqds/ag₂o/ag-zn-ce/sio₂It is placed under argon gas atmosphere and carry out 500 ~ 800 DEG C of heat Process 1 ~ 2h, after being cooled to room temperature, be immersed in Fluohydric acid. and ultrasonic 10 ~ 15min is carried out with ultrasonic power 100 ~ 150w, remove table Face local silicon dioxide, is centrifuged and is dried, obtain antibacterial powder；

3. the preparation method of the low temperature glaze modelled after an antique with purify air effect according to claim 2 is it is characterised in that walk Suddenly increase by a step between (4) and (5): take three-dimensional sponge shape Graphene ultrasonic agitation to be scattered in aqueous solution, be added dropwise over gqds/ag₂o/ag-zn-ce/sio₂In aqueous solution, three-dimensional sponge shape Graphene and gqds/ag₂o/ag-zn-ce/sio₂Weight Amount ratio is 1:1 ~ 5；Ultrasonic 60 ~ the 120min of 10 ~ 100w, standing, deionized water wash for several times, dry gqds/ag₂o/ag-zn- ce/sio₂/ Graphene antibiosis powder.

4. a kind of preparation method of the low temperature glaze modelled after an antique with purify air effect, it comprises the following steps:

Step c, glaze slip is equably applied and applies on base substrate, then in reducing atmosphere stove, natural after being incubated at 700 ~ 800 DEG C It is cooled to room temperature, obtain anion low temperature glaze modelled after an antique；

Wherein, the preparation method of described antibiotic complex is as follows:

5. the preparation method of the low temperature glaze modelled after an antique with purify air effect according to claim 4 is it is characterised in that walk Suddenly increase by a step between (3) and (4): take three-dimensional sponge shape Graphene ultrasonic agitation to be scattered in aqueous solution, be added dropwise over gqds/ag₂In o/zno aqueous solution, three-dimensional sponge shape Graphene and gqds/ag₂The weight of o/zno is than for 1:1 ~ 5；10 ~ 100w surpasses Sound 60 ~ 120min, standing, deionized water wash for several times, dry gqds/ag₂O/zno/ Graphene antibiosis powder.

6. the preparation method of the low temperature glaze modelled after an antique with purify air effect according to claim 1 or 4, its feature exists In described coloring agent is the ultrafine slag that ferrum oxide or particle diameter are less than 200 mesh；Described ultrafine slag preparation process is as follows: by ferrum Slag is roughly ground to can be ground uniformly in mortar, then carried out ball milling after 60 ~ 80 mesh sieves, and drum's speed of rotation is 1400 ~ 1600r/min, Ball-milling Time is 50 ~ 70min；Then 200 ~ 250 mesh sieves are crossed.

7. the preparation method of the low temperature glaze modelled after an antique with purify air effect according to claim 1 or 4, its feature exists In described anion complex preparation method is as follows: by 5 ~ 10% coral fossil, 10 ~ 15% tourmaline, 20 ~ 35% opals, 1 ~ 5% serpentine, 5 ~ 10% Maifanitums, 1 ~ 5% rare ice stone, 1 ~ 5% hokutolite, 1 ~ 5% Doctor king stone, 5 ~ 10% shells, 10 ~ 15% kieselguhr, 1 ~ 3% iron sesquioxide, 2 ~ 5% aluminium sesquioxide, 3 ~ 8% zirconium oxides and 1 ~ 5% zirconium phosphate mix homogeneously, add in grinding equipment Row superfine grinding, until particle diameter distribution, in 50 ~ 80nm, is sieved, is dried, you can described anion powder is obtained；5 ~ 10g is taken to bear Ion powder is scattered in 100 ~ 200ml ultra-pure water, and water bath sonicator 1 ~ 2h obtains all even stable dispersion liquid；To have carbon nanometer When the substrate of pipe reticular membrane is placed in about 8 DEG C, dispersion liquid is added in the substrate of concave shape, meanwhile, rolls around roller, make this Homogeneous dispersion is scattered in this carbon nanotube mesh film, has hydrophilic due to when CNT is near 8 DEG C, this dispersion liquid It is attracted to multiple net holes of carbon nanotube mesh film；It is warming up to about 25 DEG C, CNT has hydrophobicity and catches up with hydrone Walk to leave behind anion powder to adsorb in multiple net holes of carbon nanotube mesh film；After drying, the carbon of anion powder will be adsorbed with Nanotube reticular membrane scrapes off this substrate, obtains anion powder/CNT.

8. the preparation method of the low temperature glaze modelled after an antique with purify air effect according to claim 1 or 4, its feature exists In described Anhydrite is obtained by mixing by weight 3 ~ 5:1 ~ 2 by potassium feldspar and albite；Described carbonate by potassium carbonate, sodium carbonate, Brium carbonate, lithium carbonate and Calcium Carbonate are obtained by mixing by weight 3:1:3:2:1；Described fluoride salt is by sodium fluoride, calcium fluoride and fluorine Change lithium to be obtained by mixing by weight 4:2:1.

9. a kind of low temperature glaze modelled after an antique with purify air effect is it is characterised in that having described in claim 1 or 4 is net The preparation method changing the low temperature glaze modelled after an antique of air effect is obtained.