CN109852211A - A kind of dumb light thixotropic coating - Google Patents

A kind of dumb light thixotropic coating Download PDF

Info

Publication number
CN109852211A
CN109852211A CN201910036225.5A CN201910036225A CN109852211A CN 109852211 A CN109852211 A CN 109852211A CN 201910036225 A CN201910036225 A CN 201910036225A CN 109852211 A CN109852211 A CN 109852211A
Authority
CN
China
Prior art keywords
silicon substrate
dumb light
formulation
agent
metal oxide
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201910036225.5A
Other languages
Chinese (zh)
Inventor
刘建学
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
HUNAN KANGRUI PAINT TECHNOLOGY Co Ltd
Original Assignee
HUNAN KANGRUI PAINT TECHNOLOGY Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by HUNAN KANGRUI PAINT TECHNOLOGY Co Ltd filed Critical HUNAN KANGRUI PAINT TECHNOLOGY Co Ltd
Priority to CN201910036225.5A priority Critical patent/CN109852211A/en
Publication of CN109852211A publication Critical patent/CN109852211A/en
Pending legal-status Critical Current

Links

Landscapes

  • Paints Or Removers (AREA)

Abstract

The invention discloses a kind of dumb light thixotropic coatings, it includes the raw material of following parts by weight proportion: 50-70 parts and delustering agent 30-50 parts of resin system;The delustering agent is made of hydrophobic metal oxide;The surface texture of the oxide is any one in the group of trimethyl silicon substrate, vinyl-dimethyl base silicon substrate, acrylic dimethyl silicon substrate and dimethyl silicon substrate composition.The object of the present invention is to provide a kind of dumb light thixotropic coatings, can be used for generating matte management on matrix.

Description

A kind of dumb light thixotropic coating
Technical field
The present invention relates to a kind of dumb light thixotropic coatings.
Background technique
Metal oxide, especially silica have been added into certain coating materials, with the effect of realization " dumb light " Fruit.Apply wet film on base material be at the beginning under the action of surface tension it is flat, to form smooth surface.With film Drying and curing, viscoplasticity caused by Sol-gel phase transition increases, hinders particle and enter film, surface deformation is to adapt to Duller particle.The characteristics of this roughness remains unchanged in cured film, cured film is matte management.Due to certain metal oxygens The photoextinction of compound, especially porous silicon, produces ideal surface effect in some applications, and ideal formulation for coating material The performance that should have other additional, such as a degree of thixotropy, to enhance its practicability in various applications.
Thixotropy is a characteristic of formulation for coating material, it is related with the viscosity of coating.In fact, as formulation for coating material becomes More thixotroping, the sagging behavior of coating become less obvious.For certain applications it is necessary to a kind of tipping resistant coating composition, with to the greatest extent Amount reduce coating drip in application process, sagging and sagging.In terms of improving formulation for coating material thixotropic property, previous trial makes With many additives, such as modified resin and metal oxide.
Silica is one kind with silica (SiO2) be basic structural unit inorganic material, in many business applications In it is all very useful.Silicon exists with molecular species, such as monomer, dimer, oligomer, ring-like and polymer.In addition, dioxy SiClx can be amorphous, is crystal, aquation, solvation or drying, and can be with various particles and aggregation shape State exists.
Amorphous silica can precipitate to be formed by molecule, for example, unsaturated by cooling supersaturated solution, concentration Solution, or silica precursor (such as SiCl for passing through careful hydrolytically unstable4Solution, esters of silicon acis, (SiOR4) etc.), Si is provided (OH)4Supersaturated solution, from amorphous silica is wherein precipitated.
Thermal origin or " fumed silica ", usual partial size in 2-20 ran, are formed by gas phase.For example, silicon (usually sand) can be vaporized at 2000 DEG C or so.Anhydrous amorphous silicon particle is formed after cooling.In addition, silica can also be 1500 DEG C or so distillations.SiO is formed in the presence of reducing agent (such as coke), SiO can be oxidized to form particulate silica.It is raw The other methods for producing fumed silica include, for example, aoxidizing SiCl at high temperature4Or it burns in the case where having methane or hydrogen SiCl4
Silicon dioxde solution has polymerization behavior, and Si-O-Si key is caused to increase, and Si-OH key is reduced.In an aqueous medium, non- Crystal silicon dissolves (and/or depolymerization), is formed Si (OH)4.By polymerization, being formed in particle surface has internal Si-O-Si key and outer The discrete particle of portion's Si-OH key.Under certain conditions, the polymerized silica silicon particle being consequently formed will be further combined with formation The chain and network being made of individual particle.
Under normal circumstances, under neutral or basic conditions (pH >=7), the size of particle tends to increase, and quantity tends to reduce, And in acid condition (pH < 7), the trend of particle aggregation cluster is larger, ultimately forms three-dimensional network.The presence of salt can be reduced Interparticle electrostatic repulsion makes particle be easier to assemble under neutral or basic conditions.
" colloidal sol " word refers to the colloidal solid of dispersion, such as the dispersion of amorphous silica in an aqueous medium.Such as Fruit colloidal sol be it is stable, even across storage in several years, will not gel or precipitation, and dioxide-containing silica can reach 50% left side The right side, particle diameter is up to 300nm or so, although particle is greater than viscosity of the sinking speed depending on medium after 70nm.For example, dioxy SiClx colloidal sol can be by making particle increase to a certain size, or in sodium silicate solution (Na in weakly alkaline solution2SiO3) in Diluted acid is added, quickly mixes, until pH is down to 8-10 or so, then removes Na+(for example, ion exchange resin or electroosmose process) And it is formed.Silica solution, depending on the type of silicon, the property of granular size and particle can be in the condition of faintly acid to highly acid Lower shakiness is shaped as gel.
" gel " word refers to coherent, the rigidity, continuous three-dimensional network being made of colloidal solid.Silica hydrogel can lead to The aggregation (usually without in and under the acid condition of salt) of colloidal silica particles is crossed to form the microcosmic knot of three dimensional gel Structure.However, whether gel can form the property depending on silica under given conditions, for example, granular size and particle The property on surface.
" hydrogel " refers to a kind of gel, and hole (space of gel microstructure portion) therein is filled by water.It is similar Ground, " alcogel " word refer to the gel that alcohol is full of in pore.When gel drying forms desiccant gel, evaporation be will lead to Gel largely collapses, so that generate relative high density collapses powder.On the contrary, when gel is obtained sufficiently by gel microstructure When the mode of protection is dry, a kind of desiccant gel of low-density is formed, referred to as " aeroge ".Silica aerogel may have very not Ordinary and ideal characteristic, for example, optical clarity, extremely low density and unprecedented low thermal conductivity.
Synthesize silicon, for example, micronization silica xerogel and sediment as delustering agent, due to silicon particle surface There are silanol groups, usually hydrophilic.It is well known that this silicate to coating almost without thixotropy, result even in Other are ineffective for thixotropic additive.
By consulting domestic and foreign literature, it is thus understood that foreign countries have already passed through a variety of trials at present, by modifying the structure of silica gel, A kind of effective delustering agent is become, but very little is influenced on thixotropy.U.S.'s pa is special.No. 5221337 disclose it is organic more First alcoholic compound can produce the delustering agent to formulation for coating material thixotropy almost without negative effect to the modification of silica.So And this method still has problem, because adding thixotropy additive and delustering agent simultaneously can cause not in formulation for coating material Good interaction.
Therefore, there is still a need for a kind of formulation for coating material, this formula had both shown improved disappear when being applied to various matrixes Light effect, and show thixotropic effects.
Summary of the invention
The purpose of the present invention is can be used on matrix generating mute in view of the above problems, provide a kind of dumb light thixotropic coating Light processing.
In order to achieve the above object, the technical solution adopted by the present invention is that: it includes the raw material of following parts by weight proportion: tree 50-70 parts and delustering agent 30-50 parts of resin system;The delustering agent is made of hydrophobic metal oxide;The table of the oxide Face structure is in the group of trimethyl silicon substrate, vinyl-dimethyl base silicon substrate, acrylic dimethyl silicon substrate and dimethyl silicon substrate composition Any one.
In preferable situation, the metal oxide is aerosil, silica desiccant gel or precipitating dioxy SiClx.
In preferable situation, the resin system is from alkyd, acrylic acid, epoxy, polyurethane, polyester, cellulose and its to mix Close any one or more in object.
In preferable situation, resin system includes at least one alkyd.
In preferable situation, resin system includes at least one acrylic acid.
In preferable situation, it further includes 10-20 parts of liquid carrier.
In preferable situation, the liquid carrier is water.
In preferable situation, the liquid carrier is any one in hydro carbons, alcohols, ketone, esters, ethers and its mixture Kind is a variety of.
Metal oxide in the present invention includes silica, aluminium oxide, titanium dioxide, zirconium oxide, ceria, oxidation Magnesium and its mixture, wherein silica is preferred.This metal oxide is typically characterised by (gas phase) of Thermal origin, sinks Shallow lake, aeroge or desiccant gel, especially aeroge.Aeroge refers to that porosity is high, amorphous, organic or inorganic gel, hole Gap liquid is replaced air.The aeroge preferably includes silica, it is by using silanizing agent to hydrogel Surface carries out modification and the dry surface modification gel and prepares.According to the degree and type of silanization, technique production Silica gel may be that part is hydrophobic, it is also possible to completely it is hydrophobic.
Metal oxide is handled with silanizing agent, metal oxide shows hydrophobicity.In fact, silanizing agent assigns gold Belong to oxide particle surface silicon substrate structure.Within the scope of the present invention, any suitable silicon substrate part can be with metal oxide In conjunction with to obtain the effect.For example, suitable silicon substrate base can be obtained from the compound (such as silanizing agent) of following general formulae Group.
Wherein, free radical R is identical or different, each hydrogen or non-reacted, organic, linear, branch, circulation , saturated or unsaturated, fragrant or different fragrance free radical, preferably C1-C18, alkyl or C6-C14Aryl, preferably C1-C6Alkyl, naphthenic base, phenyl, vinyl or acrylic.Equally applicable silicon substrate group can be from formula R.sup.1.sub's It is obtained in silane.4nSiCl.sub.N or R1 4-nSi(OR2)n, wherein n=1-4, R1And R2It is same or different, Mei Geqing Or it is non-reacted, it is organically, linear, branch, circulation, it is saturated or unsaturated, fragrant or different fragrance from By base, it is preferable that preferably C1-C18, alkyl or C6-C14Aryl, preferably C1-C6Alkyl, naphthenic base, phenyl.Free radical can also To contain halogenic substituent, such as fluorine or chlorine.Most preferred silicon substrate part is trimethyl silicon substrate, vinyl-dimethyl base silicon substrate, propylene Base dimethyl silicon substrate or dimethyl silicon substrate.
Metal oxide has certain hydrophobicity after silanizing agent is handled.Hydrophobicity refers in methanol-water mixtures Metal oxide is infiltrated, the methanol volume ratio of symmetric suspension is formed.Preferred metal oxide at least 40% it is hydrophobic Property.The higher the better for hydrophobic degree, because hydrophobicity is higher would generally to bring better thixotropy effect.
Contact between metal oxide particle and silanizing agent can be realized by any suitable method.For example, Before mixing with carrier, silanizing agent can be sprayed on metal oxide particle.But metal oxide particle and silanization Contact between agent, which is preferably included in carrier or solvent (such as water) appropriate, adds at least one silane into metal oxide Agent.For example, the aqueous solution of silanizing agent can be added in the aqueous solution of metal oxide.
Silanizing agent total amount and the relative scale of aggregate metal oxide must be sufficiently high, so that sufficient amount of metal oxygen Compound particle contacts silanizing agent.Therefore, in formulation for coating material, the content of metal oxide can be excellent in 0.1-30% or so It is selected in 0.2-25% or so, preferably in 0.5-15% or so.
The thixotropy of formulation for coating material can be measured with any of technology.In the present invention, thixotropy is usually to use The measurement of sag resistance instrument, for example, 419 types or equivalent Lai Nita sag resistance applicator (ErichsenGmbH, Germany).? In this technology, a kind of formulation for coating material is applied on matrix, and is pulled down by applicator.Applicator is along its length by different Cut height composition, usually between 25-300 millimeters.When spreader is coated on substrate, paint item is formed on substrate The thickness of line, coating increases with cut height corresponding on spreader.Then horizonal base plate is rotated to be vertically, makes striped Then level visually determines the sagging behavior of every paint.The characteristics of formulation for coating material of the invention is lacking in 75mm or so Open height sag resistance.It is in practice considered as indicating behavior of dripping without sagging/nothing.It is understood that with coating thixotroping The increase of property, sagging maximum groove height, which is not detected, also will increase.
Formulation for coating material of the invention, will also be characterized by providing matte management to matrix after being applied to matrix.If needed Such matte management is wanted, formulation for coating material can be characterized with 60 degree.50 or Gloss Unit below.It is further preferred that Formulation for coating material has 60 degree of characteristic.Glossiness is 40 or less (such as: 30 or less).Many applications require matt surface. For example, the dazzle for reducing surface can reduce the chance of vision interference in school, hospital and university, and in this environment, note Meaning power is more concentrated.Over time, this surface treatment is also not easy to become ugly, because small scratch and defect are unlike light Damp surface is so obvious.
Metal oxide will exist in the form of discrete individual particle, have state of aggregation or non-agglomerated state.Metal oxidation Composition granule can have any suitable diameter.In general, the median of metal oxide is about 1-15mm.However, for Metal oxide, best median particle size is in 2-10mm or so.Alternatively, particle initially can bigger (for example, about 5 millimeters), Then required size is resolved into the manufacturing process of formulation for coating material.
Metal oxide can have any suitable surface area.In general, the surface area of metal oxide is at least 100m2/ g, preferably at least 200m2/ g, preferably at least 300m2/g.In certain embodiments, the surface area of metal oxide is at least For 400m2/ g, 500m2/ g, even at least 600m2/g.Under normal circumstances, the surface area of metal oxide does not exceed 900m2/ G, about 100-900m2/g.The surface area of metal oxide can be measured with any proper method known in the technology.In general, The surface area of metal oxide is by S.Brunauer, P.H.Emmet and I.Teller.J.Am Chemical Society, 60,309 (1938), Commonly referred to as BET method.
Metal oxide can also have any suitable tap density, such as about 0.01-0.2g/cm3.In order to measure silk Density is bored, the dry powder of known quality is transferred to 10cm3Solution in.Index cylinder, manual jolt ramming 40 times.Then body is recorded Product, density are calculated as mass/volume.
This metal oxide has any suitable porosity.Under normal conditions, the porosity of metal oxide exists 50% or more, preferably 70% or more, preferably 80% or more, since it is known that higher porosity will lead to More effective delustring.
If desired, any suitable carrier (such as solvent) may be used in formulation for coating material.Carrier is for promoting resin Application with metal oxide on suitable matrix surface.Suitable carrier includes inorganic carrier such as water and organic carrier such as carbon Hydrogen compound, alcohols, ketone, esters, ethers, aromatic series, alkane and its mixture.Any suitable carrier concn can be Occur in formulation for coating material, such as reaches as high as 80%.
If desired, formulation for coating material may further include at least one thixotropy additive.Although delustering agent is enough to assign Thixotroping needed for giving formulation for coating material and place mat effect, thixotropic additive can be added in formula, further increase formulation for coating material Thixotropy.Suitable thixotropic additive includes: chemically treated fumed silica, organo-clay, acid modified alcoholic etc.. Preferably, thixotropic additive is based on alkyd, particularly preferred amide or polyurethane-modified alkyd.In formulation for coating material, thixotroping The content of additive especially in modified resin, reaches as high as 50% generally in 0.5-5% or so.
The formulation for coating material can also include the various other additives known in the art being suitable for addition in paint formulation Any one of.Suitable additive may include, such as, cationic surfactant, anionic surfactant are (as long Alkyl benzene sulphonate and long-chain, preferably branch, alkyl sulfosuccinates), nonionic surfactant (long-chain polycyclic oxygen Ethane ether, preferably branched chain ether contain induced by alkyl hydroxybenzene, long-chain alkyl alcohol polyethylene oxide ether and fluorine-containing surfactant), curing agent (such as active halogen compound, vinyl sulfone compound, azepine pyridine compounds, epoxide, propenyl compounds, isocyanide Ester compound etc.), paint dispersions, thickener, levelling agent, defoaming agent (such as octanol, silicon based antifoam agent), foam inhibit Agent, releasing agent, foaming agent, bleeding agent, dyestuff, pigment, brightening agent (such as fluorescent whitening agent), preservative (such as P-hydroxybenzoic acid Ester compounds, benzothiazolone compound, isothiazolone compounds etc.), anti-skidding additive (such as wax and silicone resin), curing agent and Crosslinking agent, antifungal agent, the inhibitor (such as hydroxyl methanesulfonic sodium, paratoluenesulfonic acid sodium salt etc.) of yellowing, ultraviolet absorbing agent (such as has The benzotriazole compound of 2 groups of hydroxyl dialkyl phenyl organics), antioxidant (such as sterically hindered phenolic compound), antistatic agent, pH Regulator, waterproofing agent, wetting agent, dry hardening agent.
In formulation for coating material, other than metal oxide, there may also be other pigment.These pigment include calcium carbonate, Clay, alumina silicate, ureaformaldehyde filler etc. and other hydrophilic delustering agents.Other suitable pigment include aluminium oxide (such as aluminium oxide Colloidal sol, colloidal alumina, cationic oxidation aluminium or its hydrate etc.), silicate magnesium, magnesium carbonate, kaolin, talcum, calcium sulfate, Barium sulfate, titanium dioxide, zinc oxide, zinc sulphide, zinc carbonate, satin white, diatomite, calcium silicates, aluminium hydroxide, lithopone, zeolite, It is hydrated halogenated stone, magnesium hydroxide, polyolefin (such as polystyrene, polyethylene, polypropylene), plastics (such as acrylic acid), urea tree Rouge and melamine resin.When preparing tinted paint formulation, any traditional pigment can be used.These pigment include can be from The neat pigment of silicon that BASF AG (BASFAG) obtains.
Many other additives can appear in formulation for coating material, especially suitable for aqueous coating formulation.For example, coalescence Agent, defoaming agent, surfactant, antirust agent and pH adjusting agent are all suitable additives, can be added if necessary.
A kind of coalescent can promote the softening of resin in the component part drying process of formulation for coating material, and this material is It is well-known.One example of coalescent is butyl cellosolve.The coalescent of any suitable concentration can be added in formulation for coating material, Such as 1-35% or so.
By the wetting of formulation for coating material and the leveling of formulation for coating material, a kind of flowing additive can be proposed to promote matrix Wetting.Typical flowing additive is DISBERBYKBYK-301 (BYK-Chemie, Germany).It can be added in formulation for coating material any The flowing additive of debita spissitudo, such as 0.5-4% or so.
The presence of defoaming agent can reduce the bubble occurred in formulation for coating material in blending constituent.Any suitable defoaming agent It may be used in formulation for coating material of the invention.Preferred defoaming agent first is that BYK-035 (BYK-Chemie, Germany).Coating is matched The defoaming agent of any suitable concentration is added in Fang Zhongke, such as 0.01-3% or so.
Surfactant can be used to reduce the surface tension of formulation for coating material.Any suitable surfactant can be used In formulation for coating material of the invention.Preferred surfactant first is that SURFYNOL104 (AirProducts&Chemicals, Inc.).The surfactant of any debita spissitudo may be present in formulation for coating material, such as 0.01-3%.
If formulation for coating material is suitable for the surface of corrosion-vulnerable, antirust agent can be added in formulation for coating material.The present invention is suitable For various types of antirust agent.A kind of antirust agent of first choice is this FA-179 (Britain) of hamming.It can be added and appoint in formulation for coating material The antirust agent of what debita spissitudo, such as 0.01-2% or so.
PH adjusting agent can be used for controlling the pH value of formulation for coating material.The pH value of formulation for coating material, which is maintained at, to be applied in general to coating and matches In the range of side, especially in the case where intending to coat the matrix of the formula.It can be used and appoint in formulation for coating material of the invention What suitable pH adjusting agent.For example, pH value can be by adding sour (such as mineral acid, acid cation exchange resin) or alkali (such as alkali metal hydroxyl, alkalescence anion-exchange resin) is adjusted.One preferred pH-meter is TT-APM-95 (beauty State Tao Shi).The pH adjusting agent of any suitable concentration can appear in formulation for coating material, such as 1-4% or so.
The present invention provides a kind of dumb light thixotropic paint formulation, including resin system and delustering agent.The delustering agent includes hydrophobic Metal oxide, the surface texture of the oxide by trimethyl silicon substrate, vinyl-dimethyl base silicon substrate, acrylic dimethyl silicon substrate and One is selected in the group of dimethyl silicon substrate composition.In addition, the formulation for coating material has thixotropic behavior, after being coated on substrate, use The measurement of sag-resistant instrument, cut height of the coating in about 75mm be not sagging.Metal oxide and resin are mixed to form formulation for coating material. Optionally, resin and metal oxide can be mixed with suitable solvent.Above-mentioned resin, hydrophobic metal oxide, Carrier, formulation for coating material feature, are related to formulation for coating material of the invention.Other possible ingredients of above-mentioned coating formula also have similar retouch It states.
Beneficial effects of the present invention: a kind of dumb light thixotropic coating provided by the invention has thixotropic behavior, can be used for matrix Upper generation matte management, and matte effect is excellent, after being coated on substrate, is measured with sag-resistant instrument, coating is lacked about 75mm's Open height is not sagging.
The present invention is suitable for the matrix, such as timber, plastics and metal etc. of any required dumb light.
The present invention can be coated on substrate by modes such as no gas, electrostatic spraying, brushing, dip-coating, streamer coating, roller coating. It, can be using not although a coating of formulation for coating material of the invention is enough to transmit desired effect to substrate (such as matt facing) The only coating of a coating formula, they can be identical, be also possible to different.In addition, the flexibility and attachment of coating Power is also enough to shape matrix in various manufacturing operations.
Specific embodiment
Explaination further is made to the present invention by the following examples.
Embodiment 1:
It includes the raw material of following parts by weight proportion: 50 parts and 50 parts of delustering agent of resin system;The delustering agent is by two Silica aerogel composition;The surface texture of the oxide is trimethyl silicon substrate, vinyl-dimethyl base silicon substrate, acrylic diformazan Base silicon substrate and dimethyl silicon substrate composition group in any one.
Preferably, resin system includes alkyd.
Preferably, it further includes 10 parts of water.
Embodiment 2:
It includes the raw material of following parts by weight proportion: 60 parts and 40 parts of delustering agent of resin system;The delustering agent is by two Silica desiccant gel composition;The surface texture of the oxide is trimethyl silicon substrate, vinyl-dimethyl base silicon substrate, acrylic two Methylsilyl and dimethyl silicon substrate composition group in any one.
Preferably, the resin system includes acrylic acid.
Preferably, it further includes 15 parts of hydro carbons.
Embodiment 3:
It includes the raw material of following parts by weight proportion: 70 parts and 50 parts of delustering agent of resin system;The delustering agent is by sinking Shallow lake silica composition;The surface texture of the oxide is trimethyl silicon substrate, vinyl-dimethyl base silicon substrate, acrylic dimethyl Silicon substrate and dimethyl silicon substrate composition group in any one.
In preferable situation, the resin system includes polyurethane.
In preferable situation, it further includes 20 parts of ketone.
Embodiment 4:
It includes the raw material of following parts by weight proportion: 50 parts and 35 parts of delustering agent of resin system;The delustering agent is by two Silica aerogel composition;The surface texture of the oxide is trimethyl silicon substrate, vinyl-dimethyl base silicon substrate, acrylic diformazan Base silicon substrate and dimethyl silicon substrate composition group in any one.
In preferable situation, the resin system is formed using alkyd, acrylic acid, epoxy, polyurethane, polyester, cellulose Mixture.
In preferable situation, it further includes hydro carbons, alcohols, ketone, esters, 15 parts of mixture of ethers composition.
Embodiment 5:
It includes resin system and delustering agent;Delustering agent used is hydrophobic silica aerogel, and surface area is about 690m2/ g, median about 7.6mm, tap density is about 0.04g/cm3
Constituent content (weight): long oil alkyd resin 35%, thixotropy alkyd calcium resin 20%, calcium octoate 0.5%, mill base Dispersing agent 4%, high molecular surfactant 0.2%, methyl ethyl ketone oxime 0.5%, zirconium base desiccant 2.4%, aliphatic hydrocarbon 33.4%, delustering agent 3%.
After mixing these components to generate formulation for coating material, one layer of formulation for coating material is coated on wood substrate, makes it dry It is dry.Then painting layer visual inspection its quality on substrate.The study found that the formulation for coating material generates wood substrates Ideal matte management.Formulation for coating material is applying matrix or when dried base, in appearance not sagging trend.These The result shows that formulation for coating material of the invention can be used for generating matte management on matrix.
It should be noted that, in this document, the terms "include", "comprise" or its any other variant are intended to non-row His property includes, so that the process, method, article or equipment for including a series of elements not only includes those elements, and And further include other elements that are not explicitly listed, or further include for this process, method, article or equipment institute it is intrinsic Element.
A kind of dumb light thixotropic coating provided by the present invention is described in detail above, herein to original of the invention Reason and embodiment are expounded, and the above embodiments are only used to help understand, and method and its core of the invention is thought Think;At the same time, for those skilled in the art, according to the thought of the present invention, in specific embodiments and applications There will be changes, in conclusion the contents of this specification are not to be construed as limiting the invention.

Claims (8)

1. a kind of dumb light thixotropic coating, which is characterized in that it includes the raw material of following parts by weight proportion: resin system 50-70 Part and delustering agent 30-50 parts;The delustering agent is made of hydrophobic metal oxide;The surface texture of the oxide is front three Base silicon substrate, vinyl-dimethyl base silicon substrate, acrylic dimethyl silicon substrate and dimethyl silicon substrate composition group in any one.
2. a kind of dumb light thixotropic coating according to claim 1, which is characterized in that the metal oxide is silica Aeroge, silica desiccant gel or precipitated silica.
3. a kind of dumb light thixotropic coating according to claim 1, which is characterized in that the resin system is from alkyd, third Any one or more in olefin(e) acid, epoxy, polyurethane, polyester, cellulose and its mixture.
4. a kind of dumb light thixotropic coating according to claim 1, which is characterized in that resin system includes at least one alcohol Acid.
5. a kind of dumb light thixotropic coating according to claim 1, which is characterized in that resin system includes at least one propylene Acid.
6. a kind of dumb light thixotropic coating according to claim 1, which is characterized in that it further includes 10-20 parts of liquid carrier.
7. a kind of dumb light thixotropic coating according to claim 6, which is characterized in that the liquid carrier is water.
8. a kind of dumb light thixotropic coating according to claim 6, which is characterized in that the liquid carrier be hydro carbons, alcohols, Any one or more in ketone, esters, ethers and its mixture.
CN201910036225.5A 2019-01-15 2019-01-15 A kind of dumb light thixotropic coating Pending CN109852211A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910036225.5A CN109852211A (en) 2019-01-15 2019-01-15 A kind of dumb light thixotropic coating

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910036225.5A CN109852211A (en) 2019-01-15 2019-01-15 A kind of dumb light thixotropic coating

Publications (1)

Publication Number Publication Date
CN109852211A true CN109852211A (en) 2019-06-07

Family

ID=66894890

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910036225.5A Pending CN109852211A (en) 2019-01-15 2019-01-15 A kind of dumb light thixotropic coating

Country Status (1)

Country Link
CN (1) CN109852211A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116396648A (en) * 2023-05-17 2023-07-07 马保印 Paint with good uniformity and preparation method thereof

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5221337A (en) * 1990-02-14 1993-06-22 W. R. Grace & Co.-Conn. SiO2 flatting agent, process for its production and its use
CN1511183A (en) * 2001-03-15 2004-07-07 ���Ͽع����޹�˾ Matt thixotropic paint formulation
CN1633479A (en) * 2001-03-15 2005-06-29 卡伯特公司 Corrosion-resistant coating composition
JP2006045382A (en) * 2004-08-05 2006-02-16 Tsutsunaka Plast Ind Co Ltd Uv-curable anti-fogging composition
CN101613567A (en) * 2009-07-21 2009-12-30 三棵树涂料股份有限公司 A kind of environment-friendly healthy matt floor paint
WO2016080152A1 (en) * 2014-11-21 2016-05-26 デクセリアルズ株式会社 Coating composition, and super water-repellent film

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5221337A (en) * 1990-02-14 1993-06-22 W. R. Grace & Co.-Conn. SiO2 flatting agent, process for its production and its use
CN1511183A (en) * 2001-03-15 2004-07-07 ���Ͽع����޹�˾ Matt thixotropic paint formulation
CN1633479A (en) * 2001-03-15 2005-06-29 卡伯特公司 Corrosion-resistant coating composition
JP2006045382A (en) * 2004-08-05 2006-02-16 Tsutsunaka Plast Ind Co Ltd Uv-curable anti-fogging composition
CN101613567A (en) * 2009-07-21 2009-12-30 三棵树涂料股份有限公司 A kind of environment-friendly healthy matt floor paint
WO2016080152A1 (en) * 2014-11-21 2016-05-26 デクセリアルズ株式会社 Coating composition, and super water-repellent film

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116396648A (en) * 2023-05-17 2023-07-07 马保印 Paint with good uniformity and preparation method thereof

Similar Documents

Publication Publication Date Title
JP4225466B2 (en) Matte thixotrope paint formulation
JP4225467B2 (en) Corrosion resistant coating composition
CA2666335C (en) Improved depolluting coating composition
JP5374378B2 (en) Matting agent
KR100740369B1 (en) Surface Coating Composition
US10065778B2 (en) Coating composition, a process of producing a coating composition, a coated article, and a method of forming such articles
CN108727933A (en) Water-based heat-insulating coating and composition thereof
CA2906367C (en) Superhydrophilic coating composition
CN106905727A (en) Inorganic interior wall coating of functional form and preparation method thereof
CN109852211A (en) A kind of dumb light thixotropic coating
CN112080166A (en) Water-based indoor inorganic ceiling coating and preparation method thereof
JP2016150329A (en) Organic substrate having photocatalyst layer
JP2011122097A (en) Coating composition
CN111073420B (en) Water-based acrylic coating and preparation method thereof
JP2003192991A (en) Water-based coating and coated sheet obtained using the same
JP5608846B2 (en) Antifoam
WO2017159205A1 (en) Antifouling coating composition, method for forming antifouling coating layer, and method for producing ceramic building material
JP2012007099A (en) Water-repellent composition and method for producing substrate with water-repellent layer
JP2011122096A (en) Coating composition
CN109233411A (en) The production method of enamel coating

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
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20190607

WD01 Invention patent application deemed withdrawn after publication