CN106699958A - Method for polymerizing acrylate organic silicon on titanium dioxide surface - Google Patents
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/14—Methyl esters, e.g. methyl (meth)acrylate
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- C08F2/00—Processes of polymerisation
- C08F2/12—Polymerisation in non-solvents
- C08F2/16—Aqueous medium
- C08F2/22—Emulsion polymerisation
- C08F2/24—Emulsion polymerisation with the aid of emulsifying agents
- C08F2/28—Emulsion polymerisation with the aid of emulsifying agents cationic
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- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
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- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/36—Compounds of titanium
- C09C1/3607—Titanium dioxide
- C09C1/3669—Treatment with low-molecular organic compounds
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/36—Compounds of titanium
- C09C1/3607—Titanium dioxide
- C09C1/3676—Treatment with macro-molecular organic compounds
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- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/36—Compounds of titanium
- C09C1/3692—Combinations of treatments provided for in groups C09C1/3615 - C09C1/3684
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- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
- C09C3/006—Combinations of treatments provided for in groups C09C3/04 - C09C3/12
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
- C09C3/08—Treatment with low-molecular-weight non-polymer organic compounds
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- C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
- C09C3/10—Treatment with macromolecular organic compounds
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- C—CHEMISTRY; METALLURGY
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1804—C4-(meth)acrylate, e.g. butyl (meth)acrylate, isobutyl (meth)acrylate or tert-butyl (meth)acrylate
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Abstract
The invention relates to a method for polymerizing acrylate organic silicon on a titanium dioxide surface. The method is characterized by comprising the following steps: carrying out surface modification on TiO2 by using a cationic monomer, carrying out pre-emulsification on a monomer mixture composed of 15 parts of methyl methacrylate, 15 parts of butyl acrylate, 10 parts of vinyltriethoxysilane and 5 parts of alpha-methacrylic acid with 80 parts of water, 1 part of initiator ammonium persulfate and 2 parts of emulsifier to obtain a pre-emulsified mixed monomer emulsion; and heating the TiO2 slurry to 80 DEG C, adding 0.3 part of initiator ammonium persulfate, initiating the reaction for 5 minutes, slowly adding the pre-emulsified mixed monomer emulsion into the TiO2 slurry within 2-5 hours, and keeping the temperature at DEG C to carry out thermostatic reaction for 1 hour, thereby obtaining the polyacrylate-organic-silicon-coated TiO2 slurry.
Description
Technical field
The present invention relates to a kind of method that use acrylate organosilicon is polymerized in titanium dioxide surface.
Background technology
Titanium dioxide can be divided into rutile-type, Detitanium-ore-type and plate titanium-type three types, wherein plate from crystal structure
The more difficult acquisition of titanium-type titanium dioxide, it is uncommon in actual applications.Rutile-type belongs to tetragonal crystal system.There is a titanium at lattice center
Atom, there is 6 oxygen atoms around titanium atom, there is 3 titanium atoms around oxygen atom.Rutile unit cell contains two titanium dioxides
Titanium molecule, lattice is small and tight, is most stable of in three kinds of crystal formations.Also, the density and refractive index of rutile-type are also relatively
Greatly.Detitanium-ore-type also belongs to tetragonal crystal system.Titanium atom is located at octahedral center, is surround by 6 oxygen atoms, and two of which oxygen is former
Sub is closer to the distance, so occurring in the octahedral form for distorting.Detitanium-ore-type is very stable at low temperature, about at 650 DEG C
Start stabilization and the conversion of crystal formation, its conversion process receives temperature, if add additive and add the factor shadows such as which kind of additive
Ring.Optical property is one of most important characteristic of titanium dioxide, because the optical property of titanium dioxide has closely with its performance
Relation, such as refractive index, covering power, scattering force, weatherability, these are all embodying for optical property.
Coatings industry is the first large user of titanium dioxide, and titanium dioxide major part is consumed by coatings industry.Titanium dioxide
Titanium is most important pigment in coating material production, and its effect is not only to cover and decorate, it is often more important that can improve coating
Physical and chemical performance, strengthens chemical stability, improves covering power, reducing power, anticorrosive property, fast light and weatherability, strengthens the machine of film
Tool intensity and adhesive force, prevent from ftractureing and come off, and prevent ultraviolet and moisture from passing through, and extend the service life of object.
At 70-100 nanometers, its particle surface contains substantial amounts of hydroxyl to the particle size range of pigmentary titanium dioxide, it is easy to send out
Raw to reunite, the covering power of titanium dioxide can be greatly affected after reunion.So, titanium dioxide will carry out younger before
Thin grinding, adds a certain amount of dispersant in process of lapping, it is therefore an objective to separate titanium dioxide granule, such titanium dioxide hides
Lid ability can just obtain bigger performance.In addition, titanium dioxide surface is very sensitive to environment, a small amount of impurity may be caused
Scattered particle is reunited again, and the use scope of titanium dioxide is widely, and use occasion varies, slightly
Will result in scattered particle accidentally to reunite again, so necessary coat one layer of protection in titanium dioxide surface
Layer, titanium dioxide granule is kept apart, it is to avoid the reunion of titanium dioxide granule, the covering power of titanium dioxide is obtained bigger
Play.
The present invention mainly coats acrylate Organosiliconcopolymere in titanium dioxide surface, is applied in water paint.
Titanium dioxide surface polymer overmold except can reduce reunion, to greatest extent play titanium dioxide covering power in addition to, also
Some other benefits, summarize with advantages below:
(1)The reunion of titanium dioxide can be prevented, it is kept monodisperse status, strengthen its covering power, improve titanium dioxide
Utilization rate.
(2)It is easy to use, titania slurry is mixed with emulsion and adds other auxiliary agents, by two when reduction is used
The step of dry powder dispersion of titanium oxide is into slurry, and titanium dioxide is it may happen that reunite, it is impossible to effectively dispersion.
(3)Titanium dioxide transported with dry powder, used, but transported with slurry, used, it is to avoid
The generation of titanium dioxide dust, can play the effect of environmental protection, and the loss of raw material can be reduced again.
(4)Compatibility after titanium dioxide surface polymer overmold with emulsion is more preferable, can improve the performance of coating.
In order that polymer covering layer can preferably be combined with titanium dioxide surface, the present invention first with the sun with double bond from
Sub- monomer is modified to titanium dioxide surface, and modified mechanism is:Titanium dioxide surface is per se with substantial amounts of negative electrical charge, band
Cationic monomer one end of double bond carries positive charge, and titanium dioxide surface is adsorbed onto by charge effect, and the other end contains insatiable hunger
Titanium dioxide surface is also stayed in the group of double bond vinyl, then is triggered and acrylate, vinyl with initiator ammonium persulfate
Silane copolymer, finally obtained the titanium dioxide of Surface coating polyacrylate organosilicon.
The content of the invention
A kind of method that use acrylate organosilicon is polymerized in titanium dioxide surface, it is characterised in that:First to TiO2Enter
Row surface is modified, by weight by 300 parts of TiO2Powder is added in 1000 parts of water, starts agitator stirring, makes TiO2Powder
It is dispersed in water, adds 1.5 parts of dispersants, the TiO that will be obtained2Slurry carries out high speed dispersion on high speed dispersor, obtains
To monodispersed TiO2Slurry;3 parts of cationic monomers, plus 20 parts of absolute ethyl alcohol dilutions are weighed, by the second containing cationic monomer
Alcoholic solution is slowly dropped to TiO2In slurry, stir 30 minutes, obtain surface through the modifies finely dispersed TiO of cation mono2
Slurry;
Will be by 15 parts of methyl methacrylate, 15 parts of butyl acrylate, 10 parts of VTES and Alpha-Methyl third
5 parts of mix monomers of composition of olefin(e) acid carry out pre-emulsification with 80 parts of water, 1 part of initiator ammonium persulfate, 2 parts of emulsifying agent, obtain pre- breast
Change mix monomer emulsion;
By above-mentioned TiO2Slurry is heated to 80 DEG C, adds 0.3 part of initiator ammonium persulfate, and initiation reaction 5 minutes then will be pre-
The mix monomer emulsion for having emulsified is slowly added into above-mentioned TiO2In slurry, add time control at 2-5 hours, addition is finished
85 DEG C of maintenance isothermal reaction 1 hour, obtains TiO of the surface through polyacrylate silicone covering afterwards2Slurry;
Described cationic monomer be MethacryloyloxyethylTrimethyl Trimethyl Ammonium Chloride, acrylyl oxy-ethyl-trimethyl salmiac,
Acrylic acid N, N- dimethylamino ethyl ester it is therein one or more;
Described emulsifying agent is NPE ammonium sulfate;
Described TiO2Powder is anatase pigmentary TiO2;
Described dispersant is PAA.
Specific embodiment
Embodiment 1
First to TiO2Carry out surface to be modified, by 300kg anatase pigmentaries TiO2Powder is added in 1000kg water, and startup is stirred
Device stirring is mixed, makes TiO2Powder is dispersed in water, adds 1.5kg dispersants, the TiO that will be obtained2Slurry is in high speed dispersor
On carry out high speed dispersion, obtain monodispersed TiO2Slurry;3kg MethacryloyloxyethylTrimethyl Trimethyl Ammonium Chlorides are weighed, plus
20kg absolute ethyl alcohols are diluted, and the ethanol solution containing cationic monomer is slowly dropped into TiO2In slurry, stir 30 minutes, obtain
To surface through the modifies finely dispersed TiO of cation mono2Slurry;Will be by the kg of methyl methacrylate 15, butyl acrylate
The mix monomer and water 80kg, initiator mistake of 15 kg, the kg of VTES 10 and α-methacrylic acid 5kg compositions
Ammonium sulfate 1kg, emulsifying agent NPE ammonium sulfate 2kg carry out pre-emulsification, obtain pre-emulsification mix monomer emulsion;Will
Above-mentioned TiO2Slurry is heated to 80 DEG C, adds 0.3kg initiator ammonium persulfates, and initiation reaction 5 minutes is then good by pre-emulsification
Mix monomer emulsion be slowly added into above-mentioned TiO2In slurry, add time control at 2 hours, addition maintains 85 after finishing
DEG C isothermal reaction 1 hour, obtains the coated TiO in surface2Slurry.
Embodiment 2
First to TiO2Carry out surface to be modified, by 300kg anatase pigmentaries TiO2Powder is added in 1000kg water, and startup is stirred
Device stirring is mixed, makes TiO2Powder is dispersed in water, adds 1.5kg dispersants, the TiO that will be obtained2Slurry is in high speed dispersor
On carry out high speed dispersion, obtain monodispersed TiO2Slurry;Weigh 3kg acrylyl oxy-ethyl-trimethyl salmiacs, plus 20kg without
Water-ethanol is diluted, and the ethanol solution containing cationic monomer is slowly dropped into TiO2In slurry, stir 30 minutes, obtain surface
Through the modifies finely dispersed TiO of cation mono2Slurry;Will by the kg of methyl methacrylate 15, the kg of butyl acrylate 15,
The mix monomer and water 80kg, initiator ammonium persulfate of the kg of VTES 10 and α-methacrylic acid 5kg compositions
1kg, emulsifying agent NPE ammonium sulfate 2kg carry out pre-emulsification, obtain pre-emulsification mix monomer emulsion;Will be above-mentioned
TiO2Slurry is heated to 80 DEG C, adds 0.3kg initiator ammonium persulfates, initiation reaction 5 minutes, then by mixing that pre-emulsification is good
Monomer emulsions are slowly added into above-mentioned TiO2In slurry, time control is added at 5 hours, addition maintains 85 DEG C of constant temperature after finishing
Reaction 1 hour, obtains the coated TiO in surface2Slurry.
Embodiment 3
First to TiO2Carry out surface to be modified, by 300kg anatase pigmentaries TiO2Powder is added in 1000kg water, and startup is stirred
Device stirring is mixed, makes TiO2Powder is dispersed in water, adds 1.5kg dispersants, the TiO that will be obtained2Slurry is in high speed dispersor
On carry out high speed dispersion, obtain monodispersed TiO2Slurry;Weigh 3kg acrylic acid N, N- dimethylamino ethyl ester, plus 20kg without
Water-ethanol is diluted, and the ethanol solution containing cationic monomer is slowly dropped into TiO2In slurry, stir 30 minutes, obtain surface
Through the modifies finely dispersed TiO of cation mono2Slurry;Will by the kg of methyl methacrylate 15, the kg of butyl acrylate 15,
The mix monomer and water 80kg, initiator ammonium persulfate of the kg of VTES 10 and α-methacrylic acid 5kg compositions
1kg, emulsifying agent NPE ammonium sulfate 2kg carry out pre-emulsification, obtain pre-emulsification mix monomer emulsion;Will be above-mentioned
TiO2Slurry is heated to 80 DEG C, adds 0.3kg initiator ammonium persulfates, initiation reaction 5 minutes, then by mixing that pre-emulsification is good
Monomer emulsions are slowly added into above-mentioned TiO2In slurry, time control is added at 3 hours, addition maintains 85 DEG C of constant temperature after finishing
Reaction 1 hour, obtains the coated TiO in surface2Slurry.
Embodiment 4
First to TiO2Carry out surface to be modified, by 300kg anatase pigmentaries TiO2Powder is added in 1000kg water, and startup is stirred
Device stirring is mixed, makes TiO2Powder is dispersed in water, adds 1.5kg dispersants, the TiO that will be obtained2Slurry is in high speed dispersor
On carry out high speed dispersion, obtain monodispersed TiO2Slurry;3kg MethacryloyloxyethylTrimethyl Trimethyl Ammonium Chlorides are weighed, plus
20kg absolute ethyl alcohols are diluted, and the ethanol solution containing cationic monomer is slowly dropped into TiO2In slurry, stir 30 minutes, obtain
To surface through the modifies finely dispersed TiO of cation mono2Slurry;Will be by the kg of methyl methacrylate 15, butyl acrylate
The mix monomer and water 80kg, initiator mistake of 15 kg, the kg of VTES 10 and α-methacrylic acid 5kg compositions
Ammonium sulfate 1kg, emulsifying agent NPE ammonium sulfate 2kg carry out pre-emulsification, obtain pre-emulsification mix monomer emulsion;Will
Above-mentioned TiO2Slurry is heated to 80 DEG C, adds 0.3kg initiator ammonium persulfates, and initiation reaction 5 minutes is then good by pre-emulsification
Mix monomer emulsion be slowly added into above-mentioned TiO2In slurry, add time control at 4 hours, addition maintains 85 after finishing
DEG C isothermal reaction 1 hour, obtains the coated TiO in surface2Slurry.
Embodiment 5
First to TiO2Carry out surface to be modified, by 300kg anatase pigmentaries TiO2Powder is added in 1000kg water, and startup is stirred
Device stirring is mixed, makes TiO2Powder is dispersed in water, adds 1.5kg dispersants, the TiO that will be obtained2Slurry is in high speed dispersor
On carry out high speed dispersion, obtain monodispersed TiO2Slurry;Weigh 3kg acrylyl oxy-ethyl-trimethyl salmiacs, plus 20kg without
Water-ethanol is diluted, and the ethanol solution containing cationic monomer is slowly dropped into TiO2In slurry, stir 30 minutes, obtain surface
Through the modifies finely dispersed TiO of cation mono2Slurry;Will by the kg of methyl methacrylate 15, the kg of butyl acrylate 15,
The mix monomer and water 80kg, initiator ammonium persulfate of the kg of VTES 10 and α-methacrylic acid 5kg compositions
1kg, emulsifying agent NPE ammonium sulfate 2kg carry out pre-emulsification, obtain pre-emulsification mix monomer emulsion;Will be above-mentioned
TiO2Slurry is heated to 80 DEG C, adds 0.3kg initiator ammonium persulfates, initiation reaction 5 minutes, then by mixing that pre-emulsification is good
Monomer emulsions are slowly added into above-mentioned TiO2In slurry, time control is added at 4.5 hours, addition maintains 85 DEG C of perseverances after finishing
Temperature reaction 1 hour, obtains the coated TiO in surface2Slurry.
Embodiment 6
First to TiO2Carry out surface to be modified, by 300kg anatase pigmentaries TiO2Powder is added in 1000kg water, and startup is stirred
Device stirring is mixed, makes TiO2Powder is dispersed in water, adds 1.5kg dispersants, the TiO that will be obtained2Slurry is in high speed dispersor
On carry out high speed dispersion, obtain monodispersed TiO2Slurry;Weigh 3kg acrylic acid N, N- dimethylamino ethyl ester, plus 20kg without
Water-ethanol is diluted, and the ethanol solution containing cationic monomer is slowly dropped into TiO2In slurry, stir 30 minutes, obtain surface
Through the modifies finely dispersed TiO of cation mono2Slurry;Will by the kg of methyl methacrylate 15, the kg of butyl acrylate 15,
The mix monomer and water 80kg, initiator ammonium persulfate of the kg of VTES 10 and α-methacrylic acid 5kg compositions
1kg, emulsifying agent NPE ammonium sulfate 2kg carry out pre-emulsification, obtain pre-emulsification mix monomer emulsion;Will be above-mentioned
TiO2Slurry is heated to 80 DEG C, adds 0.3kg initiator ammonium persulfates, initiation reaction 5 minutes, then by mixing that pre-emulsification is good
Monomer emulsions are slowly added into above-mentioned TiO2In slurry, time control is added at 3.5 hours, addition maintains 85 DEG C of perseverances after finishing
Temperature reaction 1 hour, obtains the coated TiO in surface2Slurry.
Claims (1)
1. a kind of method that use acrylate organosilicon is polymerized in titanium dioxide surface, it is characterised in that:First to TiO2Carry out table
Face is modified, by weight by 300 parts of TiO2Powder is added in 1000 parts of water, starts agitator stirring, makes TiO2Powder is uniform
It is dispersed in water, adds 1.5 parts of dispersants, the TiO that will be obtained2Slurry carries out high speed dispersion on high speed dispersor, obtains list
Scattered TiO2Slurry;3 parts of cationic monomers, plus 20 parts of absolute ethyl alcohol dilutions are weighed, the ethanol containing cationic monomer is molten
Liquid is slowly dropped to TiO2In slurry, stir 30 minutes, obtain surface through the modifies finely dispersed TiO of cation mono2Slurry
Material;
Will be by 15 parts of methyl methacrylate, 15 parts of butyl acrylate, 10 parts of VTES and Alpha-Methyl third
5 parts of mix monomers of composition of olefin(e) acid carry out pre-emulsification with 80 parts of water, 1 part of initiator ammonium persulfate, 2 parts of emulsifying agent, obtain pre- breast
Change mix monomer emulsion;
By above-mentioned TiO2Slurry is heated to 80 DEG C, adds 0.3 part of initiator ammonium persulfate, and initiation reaction 5 minutes then will be pre-
The mix monomer emulsion for having emulsified is slowly added into above-mentioned TiO2In slurry, add time control at 2-5 hours, addition is finished
85 DEG C of maintenance isothermal reaction 1 hour, obtains TiO of the surface through polyacrylate silicone covering afterwards2Slurry;
Described cationic monomer be MethacryloyloxyethylTrimethyl Trimethyl Ammonium Chloride, acrylyl oxy-ethyl-trimethyl salmiac,
Acrylic acid N, N- dimethylamino ethyl ester it is therein one or more;
Described emulsifying agent is NPE ammonium sulfate;
Described TiO2Powder is anatase pigmentary TiO2;
Described dispersant is PAA.
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111533920A (en) * | 2020-05-11 | 2020-08-14 | 张中明 | Polyacrylate graftTiO2Modified polylactic acid antibacterial material and preparation method thereof |
CN113583503A (en) * | 2021-08-27 | 2021-11-02 | 河南佰利联新材料有限公司 | Hybrid slurry, preparation method thereof and coating |
CN114410131A (en) * | 2021-12-14 | 2022-04-29 | 河南河大纳米材料工程研究中心有限公司 | Water-phase instant titanium dioxide material and preparation method and application thereof |
CN114621607A (en) * | 2020-12-11 | 2022-06-14 | 中信钛业股份有限公司 | Preparation method of special titanium dioxide pigment for high-temperature-resistant general engineering plastics |
CN116120639A (en) * | 2023-02-03 | 2023-05-16 | 桂林桂广申巴粉体材料有限责任公司 | Carrier-free talcum powder granule and preparation method thereof |
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WO2009110848A1 (en) * | 2008-03-04 | 2009-09-11 | Agency For Science, Technology And Research | Low shrinkage multifunctional ssq resins |
WO2009141057A1 (en) * | 2008-05-23 | 2009-11-26 | Merck Patent Gmbh | Polymerisation method for producing core-shell particles |
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CN111533920A (en) * | 2020-05-11 | 2020-08-14 | 张中明 | Polyacrylate graftTiO2Modified polylactic acid antibacterial material and preparation method thereof |
CN114621607A (en) * | 2020-12-11 | 2022-06-14 | 中信钛业股份有限公司 | Preparation method of special titanium dioxide pigment for high-temperature-resistant general engineering plastics |
CN114621607B (en) * | 2020-12-11 | 2023-06-06 | 中信钛业股份有限公司 | Preparation method of high-temperature-resistant special titanium dioxide pigment for general engineering plastics |
CN113583503A (en) * | 2021-08-27 | 2021-11-02 | 河南佰利联新材料有限公司 | Hybrid slurry, preparation method thereof and coating |
CN113583503B (en) * | 2021-08-27 | 2022-12-30 | 河南佰利联新材料有限公司 | Hybrid slurry, preparation method thereof and coating |
CN114410131A (en) * | 2021-12-14 | 2022-04-29 | 河南河大纳米材料工程研究中心有限公司 | Water-phase instant titanium dioxide material and preparation method and application thereof |
CN116120639A (en) * | 2023-02-03 | 2023-05-16 | 桂林桂广申巴粉体材料有限责任公司 | Carrier-free talcum powder granule and preparation method thereof |
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