CN108795280A - A kind of wooden cabinet surface waterproofing coating - Google Patents
A kind of wooden cabinet surface waterproofing coating Download PDFInfo
- Publication number
- CN108795280A CN108795280A CN201810363235.5A CN201810363235A CN108795280A CN 108795280 A CN108795280 A CN 108795280A CN 201810363235 A CN201810363235 A CN 201810363235A CN 108795280 A CN108795280 A CN 108795280A
- Authority
- CN
- China
- Prior art keywords
- wooden cabinet
- waterproofing coating
- cabinet surface
- surface waterproofing
- tridecafluoro
- 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
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
-
- 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
-
- 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
- C09D7/63—Additives non-macromolecular organic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2227—Oxides; Hydroxides of metals of aluminium
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/011—Nanostructured additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
- C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
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)
- Chemical Kinetics & Catalysis (AREA)
- Paints Or Removers (AREA)
Abstract
The invention discloses a kind of wooden cabinet surface waterproofing coating, are related to wood furniture technical field, are made by weight of following component：Organic silicon emulsion 120-135, hydroxyl dimethyl silicone polymer 2.6-3.5, glycosyl amide are modified tridecafluoro-n-octyltriethoxysilane 5.5-5.8, oleic acid modified nano-alumina 6-10, inorganic filler 55-60, deionized water 80-90；Wooden cabinet coating prepared by the present invention not only has good uniformity, simultaneously, with good permeability and particle absorption activity, it can mutually combine closely with wood materials, greatly improve the adhesive force of film, after solidification, the hardness of film is greatly enhanced, to effectively raise the service life of film, most importantly, film coated surface hydrophobic performance can be significantly improved, the probability that wooden cabinet ontology is contacted with water can greatly be reduced, there is Signs of Mould so as to avoid wooden cabinet, and then improve the service life of wooden cabinet.
Description
Technical field
The invention belongs to wood furniture technical fields, and in particular to a kind of wooden cabinet surface waterproofing coating.
Background technology
Cabinet is configured with cabinet, hanging cupboard, high cube container three categories, and function includes washing, cooking, culinary art, four kinds of storage.Cupboard
Cabinet is generally by table top（benchtops）, door-plate, cabinet（cabinets）, kitchen appliance, sink, Hardware fitting constitute.
There are many kinds of the door-plates of existing cabinet and the material of cabinet, for example, stainless steel, multi-layer solid wood, log, fiberglass,
Acrylic board etc., material be multi-layer solid wood either log we term it wooden cabinets.
For existing wooden cabinet there is also following shortcoming, surface is vulnerable to water stain erosion, over time, easily mouldy
It is infested, the service life of wooden cabinet is greatly lowered.
Invention content
The purpose of the present invention is for existing problem, provide a kind of wooden cabinet surface waterproofing coating.
The present invention is achieved by the following technical solutions：
A kind of wooden cabinet surface waterproofing coating, is made of following component by weight：Organic silicon emulsion 120-135, hydroxyl
Base dimethyl silicone polymer 2.6-3.5, glycosyl amide are modified tridecafluoro-n-octyltriethoxysilane 5.5-5.8, oleic acid modification is received
Rice aluminium oxide 6-10, inorganic filler 55-60, deionized water 80-90.
Further, the glycosyl amide modification tridecafluoro-n-octyltriethoxysilane preparation method is：
Tridecafluoro-n-octyltriethoxysilane is mixed with gluconic acid, makees solvent with low-carbon alcohols, in 120-125 DEG C, indifferent gas
It is reacted under body atmosphere 3-4 hours, the wherein molar ratio of tridecafluoro-n-octyltriethoxysilane and gluconic acid is 3.5: 2.1-
2.5；After the completion of reaction, glycosyl amide modification tridecafluoro-n-octyltriethoxysilane is obtained by the way that solvent is evaporated off.
Further, the low-carbon alcohols are that isopropanol presses 100 with ethyl alcohol:1-3 volume ratios mix.
Further, the inert gas is neon.
Further, the oleic acid modified nano-alumina preparation method is：
(1) aluminum nitrate and gluconolactone are pressed 40:1.0-1.2 mass ratios uniformly mix, and are made into mixed solution, mixed solution
Middle aluminum nitrate concentration is 1.52-1.82mol/L, then straight to mixed solution and dripping weak base again with ultrasonication 3-5min
To mixed solution pH to 5.65, alumina sol is obtained；
(2) by alumina sol obtained by step (1) by washing, drying obtains solids to constant weight；
(3) step (2) obtained solid object is added in Muffle furnace and is calcined, calcination time is 3.5-3.8 hours, calcining temperature
Degree is 915-918 DEG C, obtains nano aluminium oxide, and after cooled to room temperature, nano aluminium oxide is pressed 30-50g：The ratio of 300mL
Example is evenly spread in toluene, after stirring evenly, then is added 3-5g oleic acid, is heated to 120-150 DEG C, continues stirring 2 hours, so
After filtered, using washes of absolute alcohol, drying to constant weight to get.
Further, the oleic acid modified nano-alumina shape of particle is that array is rodlike.
Further, the step（2）Middle ultrasonic frequency is 55kHz.
Further, the organic silicon emulsion is ionic hydroxy-silicone-oil emulsion, oil content 25.5%, pH value 6.8.
Further, the inorganic filler is bentonite.
Further, the montmorillonite is sodium bentonite, and granularity is 1200 mesh.
The present invention is modified tridecafluoro-n-octyltriethoxysilane with glycosyl amide by oleic acid modified nano-alumina and cooperates with
Effect, after enabling to coating film forming solidification, oleic acid modified nano-alumina particle is passing through modified, the phase in film forming procedure
Mutually aggregation, forms micron-sized mastoid process；And can be largely distributed in mastoid process in the micron-scale compared with the granule particles of small particle, to shape
At the micron-nanometer dual structure of similar lotus leaf surface, collaboration glycosyl amide is modified tridecafluoro-n-octyltriethoxysilane, can
Hydrophobic grouping is dramatically increased, these hydrophobic groupings play the effect of low-surface-energy wax crystalline substance in lotus leaf surface micro-enzyme electrode,
To make coating surface that " lotus leaf effect " be presented, has ultra-hydrophobicity.Through overtesting, its Static Contact of film coated surface of the present invention
Angle reaches as high as 173 ° or so, and roll angle is only 3.5 °, be water droplet when contacting coating surface, micron-nanometer dual structure
In the air layer of nanoscale thickness is only existed in intermastoid gap so that size can only be across sky much larger than the water droplet of this structure
Gas forms point contact in mastoid process, and cannot penetrate into intermastoid gap, reaches super-hydrophobic state.
The present invention has the following advantages compared with prior art：Wooden cabinet coating prepared by the present invention not only has good
Uniformity, meanwhile, have good permeability and particle absorption activity, can mutually combine closely with wood materials, greatly
The adhesive force for improving film, after solidification, the hardness of film is greatly enhanced, to effectively raise film
Service life most importantly can significantly improve film coated surface hydrophobic performance, can greatly reduce wooden cabinet ontology with
, there is Signs of Mould, and then improve the service life of wooden cabinet so as to avoid wooden cabinet in the probability of water contact.
Specific implementation mode
Embodiment 1
A kind of wooden cabinet surface waterproofing coating, is made of following component by weight：Organic silicon emulsion 120, hydroxyl are poly-
Dimethyl siloxane 2.6, glycosyl amide are modified tridecafluoro-n-octyltriethoxysilane 5.5, oleic acid modified nano-alumina 6, nothing
Machine filler 55, deionized water 80.
Further, the glycosyl amide modification tridecafluoro-n-octyltriethoxysilane preparation method is：
Tridecafluoro-n-octyltriethoxysilane is mixed with gluconic acid, makees solvent with low-carbon alcohols, in 120 DEG C, inert gas atmosphere
Lower reaction 3 hours is enclosed, the wherein molar ratio of tridecafluoro-n-octyltriethoxysilane and gluconic acid is 3.5: 2.1；Reaction is completed
Afterwards, glycosyl amide modification tridecafluoro-n-octyltriethoxysilane is obtained by the way that solvent is evaporated off.
Further, the low-carbon alcohols are that isopropanol presses 100 with ethyl alcohol:1 volume ratio mixes.
Further, the inert gas is neon.
Further, the oleic acid modified nano-alumina preparation method is：
(1) aluminum nitrate and gluconolactone are pressed 40:1.0 mass ratios uniformly mix, and are made into mixed solution, nitre in mixed solution
Sour aluminum concentration is 1.52mol/L, with ultrasonication 3min, then again to mixed solution and dripping weak base until mixed solution pH
To 5.65, alumina sol is obtained；
(2) by alumina sol obtained by step (1) by washing, drying obtains solids to constant weight；
(3) step (2) obtained solid object is added in Muffle furnace and is calcined, calcination time is 3.5 hours, and calcination temperature is
It 915 DEG C, obtains nano aluminium oxide, after cooled to room temperature, nano aluminium oxide is pressed into 30-50g：The ratio uniform of 300mL point
It is scattered in toluene, after stirring evenly, then adds 3g oleic acid, be heated to 120 DEG C, continue stirring 2 hours, then filtered, adopted
With washes of absolute alcohol, drying to constant weight to get.
Further, the oleic acid modified nano-alumina shape of particle is that array is rodlike.
Further, the step（2）Middle ultrasonic frequency is 55kHz.
Further, the organic silicon emulsion is ionic hydroxy-silicone-oil emulsion, oil content 25.5%, pH value 6.8.
Further, the inorganic filler is bentonite.
Further, the montmorillonite is sodium bentonite, and granularity is 1200 mesh.
Embodiment 2
A kind of wooden cabinet surface waterproofing coating, is made of following component by weight：Organic silicon emulsion 135, hydroxyl are poly-
Dimethyl siloxane 3.5, glycosyl amide are modified tridecafluoro-n-octyltriethoxysilane 5.8, oleic acid modified nano-alumina 10, nothing
Machine filler 60, deionized water 90.
Further, the glycosyl amide modification tridecafluoro-n-octyltriethoxysilane preparation method is：
Tridecafluoro-n-octyltriethoxysilane is mixed with gluconic acid, makees solvent with low-carbon alcohols, in 125 DEG C, inert gas atmosphere
Lower reaction 4 hours is enclosed, the wherein molar ratio of tridecafluoro-n-octyltriethoxysilane and gluconic acid is 3.5: 2.5；Reaction is completed
Afterwards, glycosyl amide modification tridecafluoro-n-octyltriethoxysilane is obtained by the way that solvent is evaporated off.
Further, the low-carbon alcohols are that isopropanol presses 100 with ethyl alcohol:3 volume ratios mix.
Further, the inert gas is neon.
Further, the oleic acid modified nano-alumina preparation method is：
(1) aluminum nitrate and gluconolactone are pressed 40:1.2 mass ratios uniformly mix, and are made into mixed solution, nitre in mixed solution
Sour aluminum concentration is 1.82mol/L, with ultrasonication 5min, then again to mixed solution and dripping weak base until mixed solution pH
To 5.65, alumina sol is obtained；
(2) by alumina sol obtained by step (1) by washing, drying obtains solids to constant weight；
(3) step (2) obtained solid object is added in Muffle furnace and is calcined, calcination time is 3.8 hours, and calcination temperature is
It 918 DEG C, obtains nano aluminium oxide, after cooled to room temperature, nano aluminium oxide is pressed into 50g：The ratio uniform of 300mL is distributed to
In toluene, after stirring evenly, then 5g oleic acid is added, be heated to 120-150 DEG C, continued stirring 2 hours, then filtered, adopted
With washes of absolute alcohol, drying to constant weight to get.
Further, the oleic acid modified nano-alumina shape of particle is that array is rodlike.
Further, the step（2）Middle ultrasonic frequency is 55kHz.
Further, the organic silicon emulsion is ionic hydroxy-silicone-oil emulsion, oil content 25.5%, pH value 6.8.
Further, the inorganic filler is bentonite.
Further, the montmorillonite is sodium bentonite, and granularity is 1200 mesh.
Embodiment 3
A kind of wooden cabinet surface waterproofing coating, is made of following component by weight：Organic silicon emulsion 128, hydroxyl are poly-
Dimethyl siloxane 2.9, glycosyl amide are modified tridecafluoro-n-octyltriethoxysilane 56, oleic acid modified nano-alumina 8, inorganic
Filler 56, deionized water 83.
Further, the glycosyl amide modification tridecafluoro-n-octyltriethoxysilane preparation method is：
Tridecafluoro-n-octyltriethoxysilane is mixed with gluconic acid, makees solvent with low-carbon alcohols, in 122 DEG C, inert gas atmosphere
Lower reaction 3.5 hours is enclosed, the wherein molar ratio of tridecafluoro-n-octyltriethoxysilane and gluconic acid is 3.5: 2.2；It has reacted
Cheng Hou obtains glycosyl amide modification tridecafluoro-n-octyltriethoxysilane by the way that solvent is evaporated off.
Further, the low-carbon alcohols are that isopropanol presses 100 with ethyl alcohol:2 volume ratios mix.
Further, the inert gas is neon.
Further, the oleic acid modified nano-alumina preparation method is：
(1) aluminum nitrate and gluconolactone are pressed 40:1.1 mass ratios uniformly mix, and are made into mixed solution, nitre in mixed solution
Sour aluminum concentration is 1.62mol/L, with ultrasonication 4min, then again to mixed solution and dripping weak base until mixed solution pH
To 5.65, alumina sol is obtained；
(2) by alumina sol obtained by step (1) by washing, drying obtains solids to constant weight；
(3) step (2) obtained solid object is added in Muffle furnace and is calcined, calcination time is 3.6 hours, and calcination temperature is
It 917 DEG C, obtains nano aluminium oxide, after cooled to room temperature, nano aluminium oxide is pressed into 40g：The ratio uniform of 300mL is distributed to
In toluene, after stirring evenly, then 4g oleic acid is added, be heated to 130 DEG C, continued stirring 2 hours, then filtered, using nothing
Water-ethanol clean, drying to constant weight to get.
Further, the oleic acid modified nano-alumina shape of particle is that array is rodlike.
Further, the step（2）Middle ultrasonic frequency is 55kHz.
Further, the organic silicon emulsion is ionic hydroxy-silicone-oil emulsion, oil content 25.5%, pH value 6.8.
Further, the inorganic filler is bentonite.
Further, the montmorillonite is sodium bentonite, and granularity is 1200 mesh.
Comparative example 1：It is differed only in embodiment 1 and replaces with glycosyl amide modification tridecafluoro-n-octyltriethoxysilane
Tridecafluoro-n-octyltriethoxysilane.
Comparative example 2：The nanometer that oleic acid modified nano-alumina is replaced with to unmodified processing is differed only in embodiment 1
Aluminium oxide.
Comparative example 3：With embodiment 1 difference lies in oleic acid modified nano-alumina shape be micron it is flower-shaped.
Brushing paint is carried out to same glass plate surface with embodiment and comparative example, coating layer thickness is 30 μm, identical
Under the conditions of be completely dried after, carry out paint film property test；
The adhesive force of film is measured by GB/T1720-79；
Static contact angle：The static contact angle of film coated surface and 4 μ L water droplets is measured with TM A-100P contact angle instruments, every time
Test is repeated 3 times；
Hardness：It is tested by pencil hardness GB/T6379-1996；
Table 1
| Film adhesive/grade | Pencil hardness/H | Static contact angle/° | |
| Embodiment 1 | 0 | 4 | 172.5 |
| Embodiment 2 | 0 | 4 | 173.3 |
| Embodiment 3 | 0 | 4 | 172.6 |
| Comparative example 1 | 3 | 3 | 145.1 |
| Comparative example 2 | 3 | 2 | 133.8 |
| Comparative example 3 | 2 | 4 | 155.6 |
As can be seen from Table 1, glycosyl amide is modified tridecafluoro-n-octyltriethoxysilane and oleic acid modified Nano oxygen in the present invention
Adhesive force, hardness and the hydrophobicity for improving coating can be cooperateed with by changing aluminium, and the form of oleic acid modified nano-alumina being capable of direct shadow
Ring the hydrophobicity of film.
Brushing paint is carried out to same glass plate surface with embodiment and comparative example, coating layer thickness is 25 μm, identical
Under the conditions of be completely dried after, carry out paint film property test；
Artificial weathering ageing resistance（GB/T9755-2001)/h ；
Table 2
| Ageing-resistant/h | |
| Embodiment 1 | ≥1350 |
| Embodiment 2 | ≥1350 |
| Embodiment 3 | ≥1350 |
| Comparative example 1 | ≥800 |
As can be seen from Table 2, glycosyl amide is modified tridecafluoro-n-octyltriethoxysilane and can effectively improve painting in the present invention
The ageing-resistant performance of film.
Claims (10)
1. a kind of wooden cabinet surface waterproofing coating, which is characterized in that be made by weight of following component：Organosilicon breast
Liquid 120-135, hydroxyl dimethyl silicone polymer 2.6-3.5, glycosyl amide are modified tridecafluoro-n-octyltriethoxysilane 5.5-
5.8, oleic acid modified nano-alumina 6-10, inorganic filler 55-60, deionized water 80-90.
2. a kind of wooden cabinet surface waterproofing coating according to claim 1, which is characterized in that the glycosyl amide changes
Property tridecafluoro-n-octyltriethoxysilane preparation method is：
Tridecafluoro-n-octyltriethoxysilane is mixed with gluconic acid, makees solvent with low-carbon alcohols, in 120-125 DEG C, indifferent gas
It is reacted under body atmosphere 3-4 hours, the wherein molar ratio of tridecafluoro-n-octyltriethoxysilane and gluconic acid is 3.5: 2.1-
2.5；After the completion of reaction, glycosyl amide modification tridecafluoro-n-octyltriethoxysilane is obtained by the way that solvent is evaporated off.
3. a kind of wooden cabinet surface waterproofing coating according to claim 2, which is characterized in that the low-carbon alcohols are different
Propyl alcohol presses 100 with ethyl alcohol:1-3 volume ratios mix.
4. a kind of wooden cabinet surface waterproofing coating according to claim 2, which is characterized in that the inert gas is
Neon.
5. a kind of wooden cabinet surface waterproofing coating according to claim 1, which is characterized in that the oleic acid modification is received
Rice alumina preparation method be：
(1) aluminum nitrate and gluconolactone are pressed 40:1.0-1.2 mass ratios uniformly mix, and are made into mixed solution, mixed solution
Middle aluminum nitrate concentration is 1.52-1.82mol/L, then straight to mixed solution and dripping weak base again with ultrasonication 3-5min
To mixed solution pH to 5.65, alumina sol is obtained；
(2) by alumina sol obtained by step (1) by washing, drying obtains solids to constant weight；
(3) step (2) obtained solid object is added in Muffle furnace and is calcined, calcination time is 3.5-3.8 hours, calcining temperature
Degree is 915-918 DEG C, obtains nano aluminium oxide, and after cooled to room temperature, nano aluminium oxide is pressed 30-50g：The ratio of 300mL
Example is evenly spread in toluene, after stirring evenly, then is added 3-5g oleic acid, is heated to 120-150 DEG C, continues stirring 2 hours, so
After filtered, using washes of absolute alcohol, drying to constant weight to get.
6. a kind of wooden cabinet surface waterproofing coating according to claim 5, which is characterized in that the oleic acid modification is received
Rice aluminium oxide particles shape is that array is rodlike.
7. a kind of wooden cabinet surface waterproofing coating according to claim 5, which is characterized in that the step（2）In
Ultrasonic frequency is 55kHz.
8. a kind of wooden cabinet surface waterproofing coating according to claim 1, which is characterized in that the organic silicon emulsion
For ionic hydroxy-silicone-oil emulsion, oil content 25.5%, pH value 6.8.
9. a kind of wooden cabinet surface waterproofing coating according to claim 1, which is characterized in that the inorganic filler is
Bentonite.
10. a kind of wooden cabinet surface waterproofing coating according to claim 1, which is characterized in that the montmorillonite is
Sodium bentonite, granularity are 1200 mesh.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201810363235.5A CN108795280A (en) | 2018-04-21 | 2018-04-21 | A kind of wooden cabinet surface waterproofing coating |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201810363235.5A CN108795280A (en) | 2018-04-21 | 2018-04-21 | A kind of wooden cabinet surface waterproofing coating |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN108795280A true CN108795280A (en) | 2018-11-13 |
Family
ID=64093723
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201810363235.5A Pending CN108795280A (en) | 2018-04-21 | 2018-04-21 | A kind of wooden cabinet surface waterproofing coating |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN108795280A (en) |
-
2018
- 2018-04-21 CN CN201810363235.5A patent/CN108795280A/en active Pending
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN105599077A (en) | Method for preparation of superhydrophobic timber on the basis of sol-gel method | |
| CN106752255A (en) | A kind of material surface protection super-hydrophobic coat spray and its preparation and application | |
| CN104449357A (en) | Transparent super-hydrophobic coating material and method for preparing transparent super-hydrophobic coating by transparent super-hydrophobic coating material | |
| CN105950053B (en) | A kind of material and its preparation process with hydrophobic function | |
| CN103464129B (en) | A kind of lanthanum doped nano TiO 2/ tourmaline composite and preparation thereof, application | |
| CN108129927A (en) | A kind of purposes of zirconium phosphate nano sheet and scratch-resistant water paint | |
| CN109487245A (en) | A kind of preparation method of super-hydrophobic aqua oxidation aluminium film | |
| CN104441127A (en) | Super-hydrophobic wood and preparation method thereof | |
| CN109975370A (en) | A kind of high sensitivity flexible humidity sensor and preparation method thereof | |
| CN107287903A (en) | A kind of preparation method of the resistant to boiling water superhydrophobic fabric available for water-oil separating | |
| CN108658130A (en) | A method of preparing iron oxide and aerosil simultaneously from iron tailings | |
| CN106634290A (en) | Formaldehyde-free environment-friendly wall paint and preparation technology thereof | |
| JPH03122162A (en) | Antibacterial electroconductive composition and antibacterial electroconductive resin | |
| CN104672967A (en) | Preparation method of colored superhydrophobic coating with outstanding corrosion resistance | |
| CN108795280A (en) | A kind of wooden cabinet surface waterproofing coating | |
| WO2019062083A1 (en) | Superhydrophobic coating layer, preparation method therefor and application thereof | |
| CN109338798A (en) | A kind of paper grade (stock) biology latex and preparation method thereof | |
| CN109575340A (en) | Flexible PET graphene coating electromagnetic shielding membrane material and preparation method thereof | |
| CN104556727B (en) | A kind of vehicle glass insulating moulding coating manufacture method | |
| CN107245281B (en) | A kind of copper ion is from sterilizing interior wall coating and preparation method thereof | |
| CN110776826A (en) | Super-hydrophobic coating with adjustable particle concentration and super-hydrophobic coating and preparation method thereof | |
| CN108314949B (en) | Nano-titanium dioxide-containing super-hydrophobic surface coating material and preparation method thereof | |
| CN104530811A (en) | Aluminum profile red powder coating even reinforcing agent and preparation method thereof | |
| CN107141932A (en) | A kind of water mildow-proof coating and preparation method thereof | |
| CN107227053A (en) | A kind of modified Yi Meng clays hydrophobic coating easy to clean and preparation method thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| RJ01 | Rejection of invention patent application after publication |
Application publication date: 20181113 |
|
| RJ01 | Rejection of invention patent application after publication |