CN105348891A - Preparation method of red luminescent coating - Google Patents
Preparation method of red luminescent coating Download PDFInfo
- Publication number
- CN105348891A CN105348891A CN201510948888.6A CN201510948888A CN105348891A CN 105348891 A CN105348891 A CN 105348891A CN 201510948888 A CN201510948888 A CN 201510948888A CN 105348891 A CN105348891 A CN 105348891A
- Authority
- CN
- China
- Prior art keywords
- graphene
- under
- ultrasonic
- preparation
- red light
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/22—Luminous paints
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
- C09D7/62—Additives non-macromolecular inorganic modified by treatment with other compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Luminescent Compositions (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
Abstract
The invention discloses a preparation method of a red luminescent coating. The preparation method comprises the following steps of (1) preparing a graphene/red phosphor composite; (2) dispersing 3-6 parts of graphene/kaoline/SiO2 composite filler and 2-4 parts of graphene/calcium carbonate/SiO2 composite filler into 15-20 parts of deionized water under ultrasonic vibration with the power of 500-800KW and stirring at the centrifugal speed of 1000-1200r/min, and treating for 90-120min to form a solution A1; dispersing 1-5 parts of the graphene/red phosphor composite into 15-20 parts of deionized water under ultrasonic vibration with the power of 500-800KW and stirring at the centrifugal speed of 1000-1200r/min, and treating for 90-120min to form a solution B1; slowly dropwise adding the solution B1 into the solution A1 under ultrasonic vibration with the power of 200-400KW and stirring at the centrifugal speed of 500-800r/min to form a mixed solution; and adding 70-80 parts of film forming matters, mixing and uniformly stirring to prepare the red luminescent coating. By using the preparation method of the red luminescent coating, the luminescent intensity and luminescent uniformity of a waterborne luminescent coating can be remarkably improved, and meanwhile the dispersibility, coating application property and storage stability of the phosphor in the coating are improved.
Description
Technical field
The present invention relates to a kind of preparation method of red light-emitting coating.
Background technology
Aqueous luminous paint is a kind of is thinner with water, it is that organic solvent exists to essentially eliminate, environmentally friendly functional paint containing long afterglow fluorescent material, has the features such as production and construction safety, nontoxicity, free from extraneous odour.Long afterglow fluorescent material can absorb the excitation energy of sunlight or light, and portion of energy is stored, and then lentamente the energy stored is discharged with the form of visible ray, after stopping excites, still can send visible ray for a long time.Be applied in water-borne coatings, the specific function that water-borne coatings is long-persistence luminous can be given, be widely used in the fields such as building decoration, communications and transportation, military installations, fire-fighting emergent, instrument.
But fluorescent material and coating density, granularity are inconsistent, and can cause precipitation, layering, the uniformity of luminance of aqueous luminous paint is poor, causes aqueous luminous paint workability and poor storage stability, and luminescent properties and/or twilight sunset effect also can be lost seriously.
Summary of the invention
In order to solve above-mentioned the deficiencies in the prior art, the invention provides a kind of preparation method of red light-emitting coating, its can significantly improve aqueous luminous paint luminous intensity, luminous evenly, improve the dispersiveness of fluorescent material in coating, coating application performance and stability in storage simultaneously.
Technical problem to be solved by this invention is achieved by the following technical programs:
A preparation method for red light-emitting coating, comprises the following steps:
(1) Graphene/red light fluorescent powder matrix material is prepared: added by 1g Graphene in 100ml deionized water, obtained graphene dispersing solution after dispersion 180 ~ 200min under 800 ~ 1000kW ultrasonic vibration and 500 ~ 800r/min centrifugal speed stir; By 25 ~ 100gY
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06nano-phosphor adds in 500ml deionized water, obtained red light fluorescent powder dispersion liquid after dispersion 240 ~ 300min under 1000 ~ 1200kW ultrasonic vibration and 800 ~ 1000r/min centrifugal speed stir; In graphene dispersing solution, slowly drip red light fluorescent powder dispersion liquid, ultrasonic 30 ~ 60min, then suction filtration, oven dry, obtained Graphene/red light fluorescent powder matrix material down 100kW is ultrasonic;
(2) by 3 ~ 6 parts of Graphene/kaolin/SiO
2compounded mix and 2 ~ 4 parts of graphene/carbon acid calcium/SiO
2compounded mix is scattered in 15 ~ 20 parts of deionized waters under 500 ~ 800KW ultrasonic vibration and 1000 ~ 1200r/min centrifugal speed stir, and process 90 ~ 120min forms solution A 1; Be scattered in 15 ~ 20 parts of deionized waters by 1 ~ 5 part of Graphene/red light fluorescent powder matrix material under 500 ~ 800KW ultrasonic vibration and 1000 ~ 1200r/min centrifugal speed stir, process 90 ~ 120min forms solution B 1; Under 200 ~ 400KW ultrasonic vibration and 500 ~ 800r/min centrifugal speed stir, slowly drip in solution B 1 to solution A 1 and form mixing solutions; Add 70 ~ 80 parts of filmogens, mixing and stirring, obtained red light-emitting coating.
The present invention has following beneficial effect: the preparation method of this red light-emitting coating can significantly improve the luminous intensity of aqueous luminous paint, luminescence evenly, improve the dispersiveness of fluorescent material in coating, coating application performance and stability in storage simultaneously, there is good economic benefit.
Embodiment
In the present invention,
(1) Graphene is obtained by following methods: get a certain amount of sour flat band ink, 1000 DEG C process 1 hour, then at 7%H in atmosphere
2nitrogen and hydrogen mixture in 1000 DEG C of in-situ reducing process 1.5 hours, add the macrogol ester of mass ratio 3% and tetracarboxylic dianhydride's dinaphthyl of mass ratio 5.0% again, the slurry that concentration is 80.0% is made into water, first under power is the ultrasonic assistant of 400W, carry out 3500 turns/min ball milling 8 hours, 2000 turns/min ball milling is carried out 4 hours under being adjusted to 200W ultrasonic wave again, be separated through supercentrifuge 10000 turns/min after ball milling, lyophilize, obtain Graphene solid.
(2) quantum dot calcium carbonate, its preparation method can prepare the method for nano calcium carbonate quantum dot with reference to a kind of microemulsion system disclosed in Chinese patent CN103570051B, specifically first prepare the nano-calcium carbonate microemulsion of 1 ~ 3nm, then through rotary evaporation also dry obtained quantum dot calcium carbonate powders.
(3) preparation method of nano-kaoline is as follows: by 150g kaolin ore with the rotating speed ball milling 60min of 1500 turns/min, then insert in 5L deionized water, add 220g Potassium ethanoate and stir 60min, suction filtration cleaning is about 7 to pH value, then with the rotating speed ball milling 60min of 1200 turns/min after drying under 80 degree of conditions, carry out 1800 turns/min ball milling under being adjusted to 300W ultrasonic wave again 1 hour, obtain the kaolin powder of particle diameter at 10 ~ 30nm.
(4) Y
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06nano fluorescent powder, preparation method thereof is as follows: (a) is by 2.4mmolNa
3vO
412H
2o is dissolved in the mixing solutions containing 10ml ethylene glycol and 3ml distilled water; B above-mentioned solution 300r/min centrifugal speed is stirred below the dropwise Y (NO of instillation containing the certain proportioning of 2.7mmol by ()
3)
36H
2o, Eu (NO
3)
3, Al (NO
3)
3(0.9:0.04:0.06) in 12ml ethylene glycol solution, then clarify to solution at 500r/min centrifugal speed stirring 5 ~ 10min, add 15ml distilled water; C reaction soln is poured in the polytetrafluoroethyllining lining autoclave that volume is 50ml by (), under vacuum conditions, and 170
oinsulation reaction 90min under C, after reaction terminates, is quickly cooled to room temperature; Gained suspension is poured out, centrifugal and obtain white precipitates by acetone and washed with de-ionized water 3 times successively; D this is deposited in 90 by ()
ounder C, dry 4h, obtains nano-phosphor; E nano-phosphor ultrasonic agitation (300 ~ 500KW ultrasonic vibration and 1000 ~ 1200r/min centrifugal speed stir) is scattered in ethanol by (); Add a certain proportion of (5:1) water and ammoniacal liquor afterwards, the mass ratio adding tetraethoxy and nano-phosphor after stirring is 1.8:1, and adjust ph is 9, and temperature of reaction is 25 DEG C, reacts 6 hours; Carry out centrifugal and obtain white precipitate 3 times by acetone and washed with de-ionized water successively; This is deposited in 90
odry 5h under C, to obtain being coated with SiO
2core-shell nano fluorescent material; F this is coated with SiO by ()
2core-shell nano fluorescent material be placed in argon gas atmosphere under carry out 800 DEG C of thermal treatment 1h, obtain fluorescent material mixture; G fluorescent material mixture is immersed in ultrasonic 1h in hydrofluoric acid by (), remove silicon-dioxide, centrifugal and dry, obtains the Y of median size 10 ~ 20nm
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06nano-phosphor.
(5) graphene/carbon acid calcium compounded mix, Graphene/kaolin compounded mix, Graphene/red light fluorescent powder matrix material, Graphene/long-afterglow fluorescent powder composite material is prepared:
The preparation method of graphene/carbon acid calcium compounded mix is as follows: added by 1g Graphene in 100ml deionized water, obtained graphene dispersing solution after dispersion 180 ~ 200min under 800 ~ 1000kW ultrasonic vibration and 500 ~ 1000r/min centrifugal speed stir; 100g quantum dot calcium carbonate is added in 500ml deionized water, obtained calcium carbonate dispersion liquid after dispersion 240 ~ 300min under 1200 ~ 1500kW ultrasonic vibration and 1000 ~ 1200r/min centrifugal speed stir; In graphene dispersing solution, slowly drip calcium carbonate dispersion liquid, ultrasonic 30 ~ 60min, then suction filtration, oven dry, obtained graphene/carbon acid calcium compounded mix down 100kW is ultrasonic.
The preparation method of Graphene/kaolin compounded mix is as follows: added by 1g Graphene in 100ml deionized water, obtained graphene dispersing solution after dispersion 180 ~ 200min under 800 ~ 1000kW ultrasonic vibration and 500 ~ 800r/min centrifugal speed stir; 50g nano kaoline is added in 500ml deionized water, obtained Dispersion of Kaolin liquid after dispersion 240 ~ 300min under 1000 ~ 1200kW ultrasonic vibration and 800 ~ 1000r/min centrifugal speed stir; In graphene dispersing solution, slowly drip Dispersion of Kaolin liquid, ultrasonic 30 ~ 60min, then suction filtration, oven dry, obtained Graphene/kaolin compounded mix down 100kW is ultrasonic.
The preparation method of Graphene/red light fluorescent powder matrix material is as follows: added by 1g Graphene in 100ml deionized water, obtained graphene dispersing solution after dispersion 180 ~ 200min under 800 ~ 1000kW ultrasonic vibration and 500 ~ 800r/min centrifugal speed stir; By 25 ~ 100gY
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06nano-phosphor adds in 500ml deionized water, obtained red light fluorescent powder dispersion liquid after dispersion 240 ~ 300min under 1000 ~ 1200kW ultrasonic vibration and 800 ~ 1000r/min centrifugal speed stir; In graphene dispersing solution, slowly drip red light fluorescent powder dispersion liquid, ultrasonic 30 ~ 60min, then suction filtration, oven dry, obtained Graphene/red light fluorescent powder matrix material down 100kW is ultrasonic.
The preparation method of Graphene/long-afterglow fluorescent powder composite material is as follows: added by 1g Graphene in 100ml deionized water, obtained graphene dispersing solution after dispersion 180 ~ 200min under 800 ~ 1000kW ultrasonic vibration and 500 ~ 800r/min centrifugal speed stir; 25 ~ 100g long persistence luminescent powder is added in 500ml deionized water, obtained long persistence luminescent powder dispersion liquid after dispersion 240 ~ 300min under 1000 ~ 1200kW ultrasonic vibration and 800 ~ 1000r/min centrifugal speed stir; Down in graphene dispersing solution, slowly drip long persistence luminescent powder dispersion liquid 100kW is ultrasonic, ultrasonic 30 ~ 60min, then suction filtration, oven dry, carry out 1050 DEG C of thermal treatment 30min under vacuum environment, thermal treatment 60min at 1250 DEG C again, obtained Graphene/long-afterglow fluorescent powder composite material.Described long persistence luminescent powder is steady persistence Sr
4al
14o
25nano-phosphor.
(6) graphene/carbon acid calcium/SiO is prepared
2compounded mix, Graphene/kaolin/SiO
2compounded mix, Graphene/red light fluorescent powder/SiO
2matrix material, Graphene/long persistence luminescent powder/SiO
2matrix material:
Graphene/carbon acid calcium/SiO
2compounded mix preparation method is as follows: be scattered in ethanol by graphene/carbon acid calcium compounded mix ultrasonic agitation (400KW ultrasonic vibration and 1000r/min centrifugal speed stir); Add a certain proportion of (5:1) water and ammoniacal liquor afterwards, the mass ratio adding tetraethoxy and graphene/carbon acid calcium compounded mix after stirring is 1.8:1, adjust ph is 9, temperature of reaction is 25 DEG C, react 5 hours, carry out centrifugal and obtain precipitation 3 times by acetone and deionized water, washed with de-ionized water successively; This is deposited in 90
odry 2h under C, to obtain being coated with SiO
2graphene/carbon acid calcium/SiO
2compounded mix.
Graphene/kaolin/SiO
2compounded mix preparation method is as follows: be scattered in ethanol by Graphene/kaolin compounded mix ultrasonic agitation (400KW ultrasonic vibration and 1000r/min centrifugal speed stir); Add a certain proportion of (5:1) water and ammoniacal liquor afterwards, the mass ratio adding tetraethoxy and Graphene/kaolin compounded mix after stirring is 1.8:1, adjust ph is 9, temperature of reaction is 25 DEG C, react 5 hours, carry out centrifugal and obtain precipitation 3 times by acetone and deionized water, washed with de-ionized water successively; This is deposited in 90
odry 2h under C, to obtain being coated with SiO
2graphene/kaolin/SiO
2compounded mix.
Graphene/red light fluorescent powder/SiO
2the preparation method of matrix material is as follows: added by 1g Graphene in 100ml deionized water, obtained graphene dispersing solution after dispersion 180 ~ 200min under 800 ~ 1000kW ultrasonic vibration and 500 ~ 800r/min centrifugal speed stir; By 25 ~ 100gY
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06nano-phosphor adds in 500ml deionized water, obtained red light fluorescent powder dispersion liquid after dispersion 240 ~ 300min under 1000 ~ 1200kW ultrasonic vibration and 800 ~ 1000r/min centrifugal speed stir; In graphene dispersing solution, slowly drip red light fluorescent powder dispersion liquid, ultrasonic 30 ~ 60min, then suction filtration, oven dry, obtained Graphene/red light fluorescent powder matrix material down 100kW is ultrasonic; 0.5g Graphene/red light fluorescent powder compound material ultrasound being stirred (300 ~ 500KW ultrasonic vibration and 1000 ~ 1200r/min centrifugal speed stir) is scattered in ethanol; Add a certain proportion of (5:1) water and ammoniacal liquor afterwards, the mass ratio adding tetraethoxy and Graphene/red light fluorescent powder matrix material after stirring is 1.8:1, and adjust ph is 9, and temperature of reaction is 25 DEG C, reacts 12 hours; Carry out centrifugal and obtain precipitation 3 times by acetone and washed with de-ionized water successively; This is deposited in 90
odry 5h under C, to obtain being coated with SiO
2core-shell composite material; This is coated with SiO
2core-shell composite material be placed in argon gas atmosphere under carry out 800 DEG C of thermal treatment 1.5h, obtain mixture; This mixture is immersed in ultrasonic 5 ~ 60min in hydrofluoric acid, removes the silicon-dioxide of part, centrifugal and dry, obtain Graphene/Y
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06fluorescent material/SiO
2matrix material.
Graphene/long persistence luminescent powder/SiO
2the preparation method of matrix material is as follows: 1g Graphene adds in 100ml deionized water by (a), obtained graphene dispersing solution after dispersion 180 ~ 200min under 800 ~ 1000kW ultrasonic vibration and 500 ~ 800r/min centrifugal speed stir; B 25 ~ 100g long persistence luminescent powder adds in 500ml deionized water by (), obtained long persistence luminescent powder dispersion liquid after dispersion 240 ~ 300min under 1000 ~ 1200kW ultrasonic vibration and 800 ~ 1000r/min centrifugal speed stir; C () slowly drips long persistence luminescent powder dispersion liquid, ultrasonic 30 ~ 60min, then suction filtration, oven dry, obtained Graphene/long-afterglow fluorescent powder composite material down 100kW is ultrasonic in graphene dispersing solution; D 0.5g Graphene/long persistence luminescent powder compound material ultrasound stirs by () (300 ~ 500KW ultrasonic vibration and 1000 ~ 1200r/min centrifugal speed stir) is scattered in ethanol; Add a certain proportion of (5:1) water and ammoniacal liquor afterwards, the mass ratio adding tetraethoxy and Graphene/long-afterglow fluorescent powder composite material after stirring is 1.8:1, and adjust ph is 9, and temperature of reaction is 25 DEG C, reacts 12 hours; Carry out centrifugal and obtain precipitation 3 times by acetone and washed with de-ionized water successively; E this is deposited in 90 by ()
odry 5h under C, to obtain being coated with SiO
2core-shell composite material; F this is coated with SiO by ()
2core-shell composite material be placed in argon gas atmosphere under carry out 800 DEG C of thermal treatment 1.5h, obtain mixture; G this mixture is immersed in ultrasonic 5 ~ 60min in hydrofluoric acid by (), remove the silicon-dioxide of part, centrifugal and dry, obtains Graphene/long persistence luminescent powder/SiO
2matrix material.
Embodiment 1
A preparation method for luminous paint, it comprises the following steps:
(1) Graphene/red light fluorescent powder matrix material is prepared: added by 1g Graphene in 100ml deionized water, obtained graphene dispersing solution disperse 180min under 800kW ultrasonic vibration and 800r/min centrifugal speed stir after; By 25gY
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06nano-phosphor adds in 500ml deionized water, obtained red light fluorescent powder dispersion liquid disperse 240min under 1000kW ultrasonic vibration and 800r/min centrifugal speed stir after; In graphene dispersing solution, slowly drip red light fluorescent powder dispersion liquid, ultrasonic 60min, then suction filtration, oven dry, obtained Graphene/red light fluorescent powder matrix material down 100kW is ultrasonic;
(2) by 6 parts of Graphene/kaolin/SiO
2compounded mix and 4 parts of graphene/carbon acid calcium/SiO
2compounded mix is scattered in 15 parts of deionized waters under 500KW ultrasonic vibration and 1200r/min centrifugal speed stir, and process 100min forms solution A 1; Be scattered in 15 parts of deionized waters by 5 parts of Graphenes/red light fluorescent powder matrix material under 500KW ultrasonic vibration and 1200r/min centrifugal speed stir, process 100min forms solution B 1; Under 400KW ultrasonic vibration and 800r/min centrifugal speed stir, slowly drip in solution B 1 to solution A 1 and form mixing solutions; Add 75 parts of water emulsion paint for internal wall, mixing and stirring, the luminous interiro wall latex paint of obtained water-based.
, there is coagulation after 2 hours in fluorescent material good dispersity, within 3 hours, occur slight coagulation, application property, stability in storage and illumination effect are good not yet.
Embodiment 2
Based on the preparation method of embodiment 1, by the Y in step (1)
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06nano-phosphor addition is revised as 50g, and all the other are constant, the luminous interiro wall latex paint of obtained water-based.
Fluorescent material is very well dispersed, and occur coagulation not yet after 4 hours, application property, stability in storage and illumination effect are good.
Embodiment 3
Based on the preparation method of embodiment 1, by the Y in step (1)
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06nano-phosphor addition is revised as 100g, and all the other are constant, the luminous interiro wall latex paint of obtained water-based.
, there is coagulation after 3 hours in fluorescent material good dispersity, within 4 hours, occur slight coagulation, application property, stability in storage and illumination effect are good not yet.
Embodiment 4
Based on the preparation method of embodiment 2, add 1 part of Graphene in the mixing solutions in step (2), all the other are constant, the luminous interiro wall latex paint of obtained water-based.
Fluorescent material is very well dispersed, and occur coagulation not yet after 5 hours, application property, stability in storage and illumination effect are good, wear resistant high-adhesion.
Comparative example 1
A preparation method for luminous paint, it comprises the following steps: by 6 parts of Graphene/kaolin/SiO
2compounded mix and 4 parts of graphene/carbon acid calcium/SiO
2compounded mix is scattered in 15 parts of deionized waters under 500KW ultrasonic vibration and 1200r/min centrifugal speed stir, and process 100min forms solution A; By 5 parts of Y
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06nano-phosphor is scattered in 15 parts of deionized waters under 500KW ultrasonic vibration and 1200r/min centrifugal speed stir, and process 100min forms solution B; Under 400KW ultrasonic vibration and 800r/min centrifugal speed stir, slowly drip in solution B to solution A and form mixing solutions; Add 75 parts of water emulsion paint for internal wall, mixing and stirring, the luminous interiro wall latex paint of obtained water-based.
Fluorescent material is dispersed general, and occur coagulation after 1 hour, application property, stability in storage and illumination effect are general.
Comparative example 2
Based on the preparation method of embodiment 1, the solution A 1 in step (2) removed, all the other are constant, the luminous interiro wall latex paint of obtained water-based.
, there is coagulation after 2 hours in fluorescent material good dispersity, within 3 hours, occurs slight coagulation, application property, poor storage stability not yet.
Comparative example 3
Based on the preparation method of embodiment 1, step (1) is revised as:
A () is by 2.4mmolNa
3vO
412H
2o is dissolved in the mixing solutions containing 10ml ethylene glycol and 3ml distilled water; B above-mentioned solution 300r/min centrifugal speed is stirred below the dropwise Y (NO of instillation containing the certain proportioning of 2.7mmol by ()
3)
36H
2o, Eu (NO
3)
3, Al (NO
3)
3(0.9:0.04:0.06) in 12ml ethylene glycol solution, then clarify to solution at 500r/min centrifugal speed stirring 5 ~ 10min, add the distilled water of 15ml containing 0.01g Graphene; C reaction soln is poured in the polytetrafluoroethyllining lining autoclave that volume is 50ml by (), under vacuum conditions, and 170
oinsulation reaction 90min under C, after reaction terminates, is quickly cooled to room temperature; Gained suspension is poured out, centrifugal and obtain precipitation by acetone and washed with de-ionized water 3 times successively; D this is deposited in 90 by ()
odry 4h under C, obtains graphene/nanometer fluorescent material matrix material; E graphene/nanometer fluorescent material compound material ultrasound stirs by () (500KW ultrasonic vibration and 1000r/min centrifugal speed stir) is scattered in ethanol; Add a certain proportion of (5:1) water and ammoniacal liquor afterwards, the mass ratio adding tetraethoxy and graphene/nanometer fluorescent material matrix material after stirring is 1.8:1, and adjust ph is 9, and temperature of reaction is 25 DEG C, reacts 6 hours; Carry out centrifugal and obtain precipitation 3 times by acetone and washed with de-ionized water successively; This is deposited in 90
odry 5h under C, to obtain being coated with SiO
2core-shell composite material; F this is coated with SiO by ()
2core-shell composite material be placed in argon gas atmosphere under carry out 800 DEG C of thermal treatment 1h, obtain mixture; G this mixture is immersed in ultrasonic 1h in hydrofluoric acid by (), remove silicon-dioxide, centrifugal and dry, obtains Graphene/Y
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06fluorescent material matrix material.
All the other are constant, the luminous interiro wall latex paint of obtained water-based.
Fluorescent material is dispersed general, and occur coagulation after 2.5 hours, application property, stability in storage and illumination effect are general.
Embodiment 5
A preparation method for luminous paint, it comprises the following steps:
(1) Graphene/red light fluorescent powder/SiO is prepared
2matrix material: 1g Graphene adds in 100ml deionized water by (a), obtained graphene dispersing solution disperse 180min under 800kW ultrasonic vibration and 800r/min centrifugal speed stir after; B () is by 25gY
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06nano-phosphor adds in 500ml deionized water, obtained red light fluorescent powder dispersion liquid disperse 240min under 1000kW ultrasonic vibration and 800r/min centrifugal speed stir after; C () slowly drips red light fluorescent powder dispersion liquid, ultrasonic 60min, then suction filtration, oven dry, obtained Graphene/red light fluorescent powder matrix material down 100kW is ultrasonic in graphene dispersing solution; D 0.5g Graphene/red light fluorescent powder compound material ultrasound stirs by () (300KW ultrasonic vibration and 1000r/min centrifugal speed stir) is scattered in ethanol; Add a certain proportion of (5:1) water and ammoniacal liquor afterwards, the mass ratio adding tetraethoxy and Graphene/red light fluorescent powder matrix material after stirring is 1.8:1, and adjust ph is 9, and temperature of reaction is 25 DEG C, reacts 12 hours; Carry out centrifugal and obtain precipitation 3 times by acetone and washed with de-ionized water successively; E this is deposited in 90 by ()
odry 5h under C, to obtain being coated with SiO
2core-shell composite material; F this is coated with SiO by ()
2core-shell composite material be placed in argon gas atmosphere under carry out 800 DEG C of thermal treatment 1.5h, obtain mixture; G this mixture is immersed in ultrasonic 5min in hydrofluoric acid by (), remove the silicon-dioxide of part, centrifugal and dry, obtains Graphene/Y
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06fluorescent material/SiO
2matrix material.
(2) by 6 parts of Graphene/kaolin/SiO
2compounded mix and 4 parts of graphene/carbon acid calcium/SiO
2compounded mix is scattered in 15 parts of deionized waters under 500KW ultrasonic vibration and 1200r/min centrifugal speed stir, and process 100min forms solution A 2; By 5 parts of Graphene/red light fluorescent powder/SiO
2matrix material is scattered in 15 parts of deionized waters under 500KW ultrasonic vibration and 1200r/min centrifugal speed stir, and process 100min forms solution B 2; Under 400KW ultrasonic vibration and 800r/min centrifugal speed stir, slowly drip in solution B 2 to solution A 2 and form mixing solutions; Add 75 parts of water emulsion paint for internal wall, mixing and stirring, the luminous interiro wall latex paint of obtained water-based.
, there is coagulation after 5 hours in fluorescent material good dispersity, application property, stability in storage, luminous intensity strong not yet.
Embodiment 6
Based on the preparation method of embodiment 5, mixture in step (1) is immersed in ultrasonic time in hydrofluoric acid and is revised as 30min, all the other are constant, the luminous interiro wall latex paint of obtained water-based.
, there is coagulation after 5 hours in fluorescent material good dispersity, application property, stability in storage, luminous intensity stronger not yet.
Embodiment 7
Based on the preparation method of embodiment 5, mixture in step (1) is immersed in ultrasonic time in hydrofluoric acid and is revised as 60min, all the other are constant, the luminous interiro wall latex paint of obtained water-based.
, there is coagulation after 5 hours in fluorescent material good dispersity, application property, stability in storage, luminous intensity strong not yet.
Comparative example 4
Based on the preparation method of embodiment 7, remove in step (1) and this is coated with SiO
2core-shell composite material be placed in argon gas atmosphere under carry out 800 DEG C of thermal treatment 1.5h; All the other are constant, the luminous interiro wall latex paint of obtained water-based.
, there is coagulation after 5 hours in fluorescent material good dispersity, application property, stability in storage, luminous intensity general not yet.
Embodiment 8
A preparation method for luminous paint, it comprises the following steps:
(1) Graphene/red light fluorescent powder/SiO is prepared
2matrix material: 1g Graphene adds in 100ml deionized water by (a), obtained graphene dispersing solution disperse 180min under 800kW ultrasonic vibration and 800r/min centrifugal speed stir after; B () is by 25gY
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06nano-phosphor adds in 500ml deionized water, obtained red light fluorescent powder dispersion liquid disperse 240min under 1000kW ultrasonic vibration and 800r/min centrifugal speed stir after; C () slowly drips red light fluorescent powder dispersion liquid, ultrasonic 60min, then suction filtration, oven dry, obtained Graphene/red light fluorescent powder matrix material down 100kW is ultrasonic in graphene dispersing solution; D 0.5g Graphene/red light fluorescent powder compound material ultrasound stirs by () (300KW ultrasonic vibration and 1000r/min centrifugal speed stir) is scattered in ethanol; Add a certain proportion of (5:1) water and ammoniacal liquor afterwards, the mass ratio adding tetraethoxy and Graphene/red light fluorescent powder matrix material after stirring is 1.8:1, and adjust ph is 9, and temperature of reaction is 25 DEG C, reacts 12 hours; Carry out centrifugal and obtain precipitation 3 times by acetone and washed with de-ionized water successively; E this is deposited in 90 by ()
odry 5h under C, to obtain being coated with SiO
2core-shell composite material; F this is coated with SiO by ()
2core-shell composite material be placed in argon gas atmosphere under carry out 800 DEG C of thermal treatment 1.5h, obtain mixture; G this mixture is immersed in ultrasonic 5min in hydrofluoric acid by (), remove the silicon-dioxide of part, centrifugal and dry, obtains Graphene/Y
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06fluorescent material/SiO
2matrix material.
(2) Graphene/long-afterglow fluorescent powder composite material is prepared: added by 1g Graphene in 100ml deionized water, obtained graphene dispersing solution disperse 180min under 1000kW ultrasonic vibration and 800r/min centrifugal speed stir after; 25g long persistence luminescent powder is added in 500ml deionized water, obtained long persistence luminescent powder dispersion liquid disperse 300min under 1000kW ultrasonic vibration and 800r/min centrifugal speed stir after; Down in graphene dispersing solution, slowly drip long persistence luminescent powder dispersion liquid 100kW is ultrasonic, ultrasonic 60min, then suction filtration, oven dry, carry out 1050 DEG C of thermal treatment 30min under vacuum environment, thermal treatment 60min at 1250 DEG C again, obtained Graphene/long-afterglow fluorescent powder composite material.
(3) by 6 parts of Graphene/kaolin/SiO
2compounded mix and 4 parts of graphene/carbon acid calcium/SiO
2compounded mix is scattered in 15 parts of deionized waters under 500KW ultrasonic vibration and 1200r/min centrifugal speed stir, and process 100min forms solution A 3; By 5 parts of Graphene/red light fluorescent powder/SiO
2matrix material is scattered in 15 parts of deionized waters under 500KW ultrasonic vibration and 1200r/min centrifugal speed stir, and process 100min forms solution B 3; Be scattered in 15 parts of deionized waters by 5 parts of Graphenes/long-afterglow fluorescent powder composite material under 500KW ultrasonic vibration and 1200r/min centrifugal speed stir, process 100min forms solution C 1; Under 400KW ultrasonic vibration and 800r/min centrifugal speed stir, slowly dropping solution B 3, C1 form mixing solutions to solution A 3 respectively; Add 75 parts of water emulsion paint for internal wall, mixing and stirring, the luminous interiro wall latex paint of obtained water-based.
, there is coagulation after 4 hours in fluorescent material good dispersity, 5 as a child occurred coagulation not yet, and application property, stability in storage, luminous intensity are stronger; Sunset glow is for up to 5h, and intensity is good, and uniformity of luminance is general.
Embodiment 9
Based on the preparation method of embodiment 8, the long persistence luminescent powder addition in step (2) is revised as 50g, and all the other are constant, the luminous interiro wall latex paint of obtained water-based.
, there is coagulation after 5 hours in fluorescent material good dispersity, application property, stability in storage and luminous intensity stronger not yet; Sunset glow is for up to 10h, and intensity is good, and uniformity of luminance is better.
Embodiment 10
Based on the preparation method of embodiment 8, the long persistence luminescent powder addition in step (2) is revised as 100g, and all the other are constant, the luminous interiro wall latex paint of obtained water-based.
, there is coagulation after 3 hours in fluorescent material good dispersity, 4 as a child occurred coagulation not yet, and application property, stability in storage and luminous intensity are stronger; Sunset glow is for up to 10h, and intensity is good, and uniformity of luminance is general.
Embodiment 11
Based on the preparation method of embodiment 8, add 1 part of Graphene in mixing solutions in step (3), all the other are constant, the luminous interiro wall latex paint of obtained water-based.
, there is coagulation after 5 hours in fluorescent material good dispersity, application property, stability in storage and luminous intensity are comparatively strong, wear resistant high-adhesion not yet; The sunset glow time reaches 10h, and intensity is good, and uniformity of luminance is better.
Comparative example 5
Based on the preparation method of embodiment 11, remove step (2), in step (3) Graphene/long-afterglow fluorescent powder composite material is replaced to long persistence luminescent powder, all the other are constant, the luminous interiro wall latex paint of obtained water-based.
Fluorescent material dispersiveness is very general, and occur coagulation not yet after 2 hours, 3 as a child occurred coagulation, and application property, stability in storage and luminous intensity are good; The sunset glow time is short, and intensity is general, non-uniform light.
Embodiment 12
Based on the preparation method of embodiment 8, Graphene/long-afterglow fluorescent powder composite material prepared by step (2) and be revised as and prepare Graphene/long persistence luminescent powder/SiO
2matrix material, concrete preparation process: 1g Graphene adds in 100ml deionized water by (a), obtained graphene dispersing solution disperse 200min under 1000kW ultrasonic vibration and 500r/min centrifugal speed stir after; B 25g long persistence luminescent powder adds in 500ml deionized water by (), obtained long persistence luminescent powder dispersion liquid disperse 240min under 1000kW ultrasonic vibration and 1000r/min centrifugal speed stir after; C () slowly drips long persistence luminescent powder dispersion liquid down 100kW is ultrasonic in graphene dispersing solution, ultrasonic 60min, then suction filtration, oven dry, carry out 1050 DEG C of thermal treatment 30min under vacuum environment, thermal treatment 60min at 1250 DEG C again, obtained Graphene/long-afterglow fluorescent powder composite material; D 0.5g Graphene/long persistence luminescent powder compound material ultrasound stirs by () (500KW ultrasonic vibration and 1000r/min centrifugal speed stir) is scattered in ethanol; Add a certain proportion of (5:1) water and ammoniacal liquor afterwards, the mass ratio adding tetraethoxy and Graphene/long-afterglow fluorescent powder composite material after stirring is 1.8:1, and adjust ph is 9, and temperature of reaction is 25 DEG C, reacts 12 hours; Carry out centrifugal and obtain precipitation 3 times by acetone and washed with de-ionized water successively; E this is deposited in 90 by ()
odry 5h under C, to obtain being coated with SiO
2core-shell composite material; F this is coated with SiO by ()
2core-shell composite material be placed in argon gas atmosphere under carry out 800 DEG C of thermal treatment 1.5h, obtain mixture; G this mixture is immersed in ultrasonic 5min in hydrofluoric acid by (), remove the silicon-dioxide of part, centrifugal and dry, obtains Graphene/long persistence luminescent powder/SiO
2matrix material;
All the other are constant, the luminous interiro wall latex paint of obtained water-based.
, there is coagulation after 5 hours in fluorescent material good dispersity, application property, stability in storage, luminous intensity comparatively strong not yet, and sunset glow is for up to 11h, and intensity is strong, and uniformity of luminance is good.
Embodiment 13
Based on the preparation method of embodiment 12, mixture in step (2) is immersed in ultrasonic time in hydrofluoric acid and is revised as 30min, all the other are constant, the luminous interiro wall latex paint of obtained water-based.
, there is coagulation after 5 hours in fluorescent material good dispersity, application property, stability in storage, luminous intensity comparatively strong not yet, and sunset glow is for up to 12h, and intensity is comparatively strong, and uniformity of luminance is better.
Embodiment 14
Based on the preparation method of embodiment 12, mixture in step (2) is immersed in ultrasonic time in hydrofluoric acid and is revised as 60min, all the other are constant, the luminous interiro wall latex paint of obtained water-based.
, there is coagulation after 5 hours in fluorescent material good dispersity, application property, stability in storage, red light-emitting intensity comparatively strong not yet, and sunset glow is for up to 10.5h, and intensity is strong, and uniformity of luminance is good.
Comparative example 6
Based on the preparation method of embodiment 14, remove in step (2) and this is coated with SiO
2core-shell composite material be placed in argon gas atmosphere under carry out 800 DEG C of thermal treatment 1.5h; All the other are constant, the luminous interiro wall latex paint of obtained water-based.
, there is coagulation after 5 hours in fluorescent material good dispersity, application property, stability in storage, red light-emitting intensity comparatively strong not yet, and sunset glow is for up to 10h, and intensity is general, and uniformity of luminance is poor.
The above embodiment only have expressed embodiments of the present invention; it describes comparatively concrete and detailed; but therefore can not be interpreted as the restriction to the scope of the claims of the present invention; in every case the technical scheme adopting the form of equivalent replacement or equivalent transformation to obtain, all should drop within protection scope of the present invention.
Claims (8)
1. a preparation method for red light-emitting coating, comprises the following steps:
(1) Graphene/red light fluorescent powder matrix material is prepared: added by 1g Graphene in 100ml deionized water, obtained graphene dispersing solution after dispersion 180 ~ 200min under 800 ~ 1000kW ultrasonic vibration and 500 ~ 800r/min centrifugal speed stir; By 25 ~ 100gY
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06nano-phosphor adds in 500ml deionized water, obtained red light fluorescent powder dispersion liquid after dispersion 240 ~ 300min under 1000 ~ 1200kW ultrasonic vibration and 800 ~ 1000r/min centrifugal speed stir; In graphene dispersing solution, slowly drip red light fluorescent powder dispersion liquid, ultrasonic 30 ~ 60min, then suction filtration, oven dry, obtained Graphene/red light fluorescent powder matrix material down 100kW is ultrasonic;
(2) by 3 ~ 6 parts of Graphene/kaolin/SiO
2compounded mix and 2 ~ 4 parts of graphene/carbon acid calcium/SiO
2compounded mix is scattered in 15 ~ 20 parts of deionized waters under 500 ~ 800KW ultrasonic vibration and 1000 ~ 1200r/min centrifugal speed stir, and process 90 ~ 120min forms solution A 1; Be scattered in 15 ~ 20 parts of deionized waters by 1 ~ 5 part of Graphene/red light fluorescent powder matrix material under 500 ~ 800KW ultrasonic vibration and 1000 ~ 1200r/min centrifugal speed stir, process 90 ~ 120min forms solution B 1; Under 200 ~ 400KW ultrasonic vibration and 500 ~ 800r/min centrifugal speed stir, slowly drip in solution B 1 to solution A 1 and form mixing solutions; Add 70 ~ 80 parts of filmogens, mixing and stirring, obtained red light-emitting coating.
2. the preparation method of red light-emitting coating according to claim 1, is characterized in that, described Graphene is obtained by following methods: get a certain amount of sour flat band ink, 1000 DEG C process 1 hour, then at 7%H in atmosphere
2nitrogen and hydrogen mixture in 1000 DEG C of in-situ reducing process 1.5 hours, add the macrogol ester of mass ratio 3% and tetracarboxylic dianhydride's dinaphthyl of mass ratio 5.0% again, the slurry that concentration is 80.0% is made into water, first under power is the ultrasonic assistant of 400W, carry out 3500 turns/min ball milling 8 hours, 2000 turns/min ball milling is carried out 4 hours under being adjusted to 200W ultrasonic wave again, be separated through supercentrifuge 10000 turns/min after ball milling, lyophilize, obtain Graphene solid.
3. the preparation method of red light-emitting coating according to claim 1, is characterized in that, described Y
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06nano fluorescent powder, preparation method thereof is as follows: (a) is by 2.4mmolNa
3vO
412H
2o is dissolved in the mixing solutions containing 10ml ethylene glycol and 3ml distilled water; B above-mentioned solution 300r/min centrifugal speed is stirred below the dropwise Y (NO of instillation containing the certain proportioning of 2.7mmol by ()
3)
36H
2o, Eu (NO
3)
3, Al (NO
3)
312ml ethylene glycol solution in, then 500r/min centrifugal speed stir 5 ~ 10min clarify to solution, add 15ml distilled water; C reaction soln is poured in the polytetrafluoroethyllining lining autoclave that volume is 50ml by (), under vacuum conditions, and 170
oinsulation reaction 90min under C, after reaction terminates, is quickly cooled to room temperature; Gained suspension is poured out, centrifugal and obtain white precipitates by acetone and washed with de-ionized water 3 times successively; D this is deposited in 90 by ()
ounder C, dry 4h, obtains nano-phosphor; E nano-phosphor ultrasonic agitation is scattered in ethanol by (); Add a certain proportion of water and ammoniacal liquor afterwards, the mass ratio adding tetraethoxy and nano-phosphor after stirring is 1.8:1, and adjust ph is 9, and temperature of reaction is 25 DEG C, reacts 6 hours; Carry out centrifugal and obtain white precipitate 3 times by acetone and washed with de-ionized water successively; This is deposited in 90
odry 5h under C, to obtain being coated with SiO
2core-shell nano fluorescent material; F this is coated with SiO by ()
2core-shell nano fluorescent material be placed in argon gas atmosphere under carry out 800 DEG C of thermal treatment 1h, obtain fluorescent material mixture; G fluorescent material mixture is immersed in ultrasonic 1h in hydrofluoric acid by (), remove silicon-dioxide, centrifugal and dry, obtains the Y of median size 10 ~ 20nm
0.9vO
4: Eu
3+ 0.04, Al
3+ 0.06nano-phosphor.
4. the preparation method of red light-emitting coating according to claim 1, is characterized in that, graphene/carbon acid calcium/SiO
2compounded mix preparation method is as follows: be scattered in ethanol by graphene/carbon acid calcium compounded mix ultrasonic agitation; Add a certain proportion of water and ammoniacal liquor afterwards, the mass ratio adding tetraethoxy and graphene/carbon acid calcium compounded mix after stirring is 1.8:1, adjust ph is 9, temperature of reaction is 25 DEG C, react 5 hours, carry out centrifugal and obtain precipitation 3 times by acetone and deionized water, washed with de-ionized water successively; This is deposited in 90
odry 2h under C, to obtain being coated with SiO
2graphene/carbon acid calcium/SiO
2compounded mix.
5. the preparation method of red light-emitting coating according to claim 4, it is characterized in that, the preparation method of described graphene/carbon acid calcium compounded mix is as follows: added by 1g Graphene in 100ml deionized water, obtained graphene dispersing solution after dispersion 180 ~ 200min under 800 ~ 1000kW ultrasonic vibration and 500 ~ 1000r/min centrifugal speed stir; 100g quantum dot calcium carbonate is added in 500ml deionized water, obtained calcium carbonate dispersion liquid after dispersion 240 ~ 300min under 1200 ~ 1500kW ultrasonic vibration and 1000 ~ 1200r/min centrifugal speed stir; In graphene dispersing solution, slowly drip calcium carbonate dispersion liquid, ultrasonic 30 ~ 60min, then suction filtration, oven dry, obtained graphene/carbon acid calcium compounded mix down 100kW is ultrasonic.
6. the preparation method of red light-emitting coating according to claim 1, is characterized in that, Graphene/kaolin/SiO
2compounded mix preparation method is as follows: by Graphene/kaolin compounded mix ultrasonic agitation is scattered in ethanol; Add a certain proportion of water and ammoniacal liquor afterwards, the mass ratio adding tetraethoxy and Graphene/kaolin compounded mix after stirring is 1.8:1, adjust ph is 9, temperature of reaction is 25 DEG C, react 5 hours, carry out centrifugal and obtain precipitation 3 times by acetone and deionized water, washed with de-ionized water successively; This is deposited in 90
odry 2h under C, to obtain being coated with SiO
2graphene/kaolin/SiO
2compounded mix.
7. the preparation method of red light-emitting coating according to claim 6, it is characterized in that, the preparation method of described Graphene/kaolin compounded mix is as follows: added by 1g Graphene in 100ml deionized water, obtained graphene dispersing solution after dispersion 180 ~ 200min under 800 ~ 1000kW ultrasonic vibration and 500 ~ 800r/min centrifugal speed stir; 50g nano kaoline is added in 500ml deionized water, obtained Dispersion of Kaolin liquid after dispersion 240 ~ 300min under 1000 ~ 1200kW ultrasonic vibration and 800 ~ 1000r/min centrifugal speed stir; In graphene dispersing solution, slowly drip Dispersion of Kaolin liquid, ultrasonic 30 ~ 60min, then suction filtration, oven dry, obtained Graphene/kaolin compounded mix down 100kW is ultrasonic.
8. the preparation method of red light-emitting coating according to claim 7, it is characterized in that, the preparation method of described nano-kaoline is as follows: by 150g kaolin ore with the rotating speed ball milling 60min of 1500 turns/min, then insert in 5L deionized water, add 220g Potassium ethanoate and stir 60min, suction filtration cleaning is about 7 to pH value, then with the rotating speed ball milling 60min of 1200 turns/min after drying under 80 degree of conditions, carry out 1800 turns/min ball milling under being adjusted to 300W ultrasonic wave again 1 hour, obtain the kaolin powder of particle diameter at 10 ~ 30nm.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201510948888.6A CN105348891A (en) | 2015-12-18 | 2015-12-18 | Preparation method of red luminescent coating |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201510948888.6A CN105348891A (en) | 2015-12-18 | 2015-12-18 | Preparation method of red luminescent coating |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN105348891A true CN105348891A (en) | 2016-02-24 |
Family
ID=55324964
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201510948888.6A Pending CN105348891A (en) | 2015-12-18 | 2015-12-18 | Preparation method of red luminescent coating |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN105348891A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113061433A (en) * | 2021-03-17 | 2021-07-02 | 黄石 | Method for manufacturing phosphor material and lighting equipment |
| CN115678541A (en) * | 2022-09-29 | 2023-02-03 | 广州珠江光电新材料有限公司 | High-performance special blue-green fluorescent powder and preparation method thereof |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5246781A (en) * | 1991-10-17 | 1993-09-21 | Samsung Electron Devices Co., Ltd. | Pigment coated phosphor and method for manufacturing same |
| CN101284657A (en) * | 2008-05-20 | 2008-10-15 | 浙江理工大学 | Synthesis method of nano-fluorescent powder mixed with europium yttrium phosphate-vanadate |
| CN103275524A (en) * | 2013-05-27 | 2013-09-04 | 淮北师范大学 | Preparation method of graphene kaolin composite nanometer rubber fillers |
| CN103626168A (en) * | 2013-09-28 | 2014-03-12 | 余泉茂 | Preparation method of graphene/oxidized graphene |
| CN104804627A (en) * | 2015-04-15 | 2015-07-29 | 青岛保利康新材料有限公司 | Durable sign coating |
-
2015
- 2015-12-18 CN CN201510948888.6A patent/CN105348891A/en active Pending
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5246781A (en) * | 1991-10-17 | 1993-09-21 | Samsung Electron Devices Co., Ltd. | Pigment coated phosphor and method for manufacturing same |
| CN101284657A (en) * | 2008-05-20 | 2008-10-15 | 浙江理工大学 | Synthesis method of nano-fluorescent powder mixed with europium yttrium phosphate-vanadate |
| CN103275524A (en) * | 2013-05-27 | 2013-09-04 | 淮北师范大学 | Preparation method of graphene kaolin composite nanometer rubber fillers |
| CN103626168A (en) * | 2013-09-28 | 2014-03-12 | 余泉茂 | Preparation method of graphene/oxidized graphene |
| CN104804627A (en) * | 2015-04-15 | 2015-07-29 | 青岛保利康新材料有限公司 | Durable sign coating |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113061433A (en) * | 2021-03-17 | 2021-07-02 | 黄石 | Method for manufacturing phosphor material and lighting equipment |
| CN115678541A (en) * | 2022-09-29 | 2023-02-03 | 广州珠江光电新材料有限公司 | High-performance special blue-green fluorescent powder and preparation method thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN105348890A (en) | Preparation method of light-emitting composite paint | |
| CN105419309A (en) | Preparation method of luminescent polyamide composite material | |
| EP2212401B1 (en) | Method for the production of coated luminescent substances | |
| CN103436249A (en) | Organic silicon wrapped fluorescent powder for light emitting coating and preparation method and application thereof | |
| CN106544025B (en) | A kind of preparation method of rear-earth-doped gadolinium oxysulfide fluorescent powder | |
| CN102775985B (en) | There is a Sr2MgSi2O7:Eu2+ for long-persistence luminous function, the synthetic method of Dy3+ nano wire | |
| CN103450876B (en) | Inorganic oxide coated fluorescent powder and preparation method thereof | |
| CN105368132A (en) | Noctilucent printing ink and preparation method thereof | |
| CN102206490B (en) | Preparation method for core-shell structure red phosphor, and core-shell structure red phosphor prepared by using the same | |
| CN105348891A (en) | Preparation method of red luminescent coating | |
| CN106893433B (en) | The spontaneous cursor line in tunnel and coating | |
| CN104263014A (en) | Preparing method of high-purity active calcium carbonate used for coating | |
| CN112322286B (en) | Rare earth ion doped nano calcium carbonate luminescent material with different morphologies as well as preparation method and application thereof | |
| CN105400181A (en) | Preparation method of noctilucent polyamide composite material | |
| EP2578661B1 (en) | Preparation methods of fluorescent materials used in field emission | |
| CN105419443A (en) | Preparation method of luminescent composite coating | |
| CN105504938A (en) | Preparation method of red-light luminous coating | |
| CN107805495B (en) | Preparation method of high-brightness zinc-manganese sulfide nano fluorescent powder | |
| CN109734940A (en) | A kind of preparation method of the luminous canopy film of rare earth silicate base composite red color | |
| CN105348904A (en) | Printing ink | |
| KR100785089B1 (en) | The blue phosphor of cacium strontium magnesium silicate and preparation method thereof | |
| CN103074061A (en) | Synthetic method of rare earth nanometer nuclear shell spherical particle luminescent material | |
| CN105419478A (en) | Luminous printing ink and preparation method thereof | |
| CN103923658A (en) | Metal particle-doped hollow structure orthophosphate luminescence material and preparation method thereof | |
| CN112500854A (en) | Processing method of silicon dioxide nanoparticles for blue-green fluorescent powder |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| RJ01 | Rejection of invention patent application after publication | ||
| RJ01 | Rejection of invention patent application after publication |
Application publication date: 20160224 |