CN113321442A - Method for preparing redispersible latex powder by taking modified silicone-acrylic emulsion as raw material - Google Patents
Method for preparing redispersible latex powder by taking modified silicone-acrylic emulsion as raw material Download PDFInfo
- Publication number
- CN113321442A CN113321442A CN202110783447.0A CN202110783447A CN113321442A CN 113321442 A CN113321442 A CN 113321442A CN 202110783447 A CN202110783447 A CN 202110783447A CN 113321442 A CN113321442 A CN 113321442A
- Authority
- CN
- China
- Prior art keywords
- agent
- modified silicone
- latex powder
- preparing
- redispersible latex
- 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
- 239000000843 powder Substances 0.000 title claims abstract description 77
- 239000000839 emulsion Substances 0.000 title claims abstract description 57
- 239000004816 latex Substances 0.000 title claims abstract description 46
- 229920000126 latex Polymers 0.000 title claims abstract description 46
- 239000002994 raw material Substances 0.000 title claims abstract description 22
- 238000000034 method Methods 0.000 title claims abstract description 21
- 239000000178 monomer Substances 0.000 claims abstract description 30
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000011258 core-shell material Substances 0.000 claims abstract description 8
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 8
- 239000012752 auxiliary agent Substances 0.000 claims abstract description 5
- 230000002194 synthesizing effect Effects 0.000 claims abstract description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 25
- 238000006243 chemical reaction Methods 0.000 claims description 22
- 238000005507 spraying Methods 0.000 claims description 18
- 239000011259 mixed solution Substances 0.000 claims description 17
- 239000003795 chemical substances by application Substances 0.000 claims description 16
- 239000000084 colloidal system Substances 0.000 claims description 16
- 238000002360 preparation method Methods 0.000 claims description 13
- 230000001681 protective effect Effects 0.000 claims description 12
- 239000003995 emulsifying agent Substances 0.000 claims description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical group [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
- 238000005516 engineering process Methods 0.000 claims description 9
- 150000004756 silanes Chemical class 0.000 claims description 9
- 239000002518 antifoaming agent Substances 0.000 claims description 8
- 239000003999 initiator Substances 0.000 claims description 8
- 239000003054 catalyst Substances 0.000 claims description 7
- 239000002270 dispersing agent Substances 0.000 claims description 7
- 239000006260 foam Substances 0.000 claims description 7
- 239000003112 inhibitor Substances 0.000 claims description 7
- 239000004094 surface-active agent Substances 0.000 claims description 7
- 150000001252 acrylic acid derivatives Chemical group 0.000 claims description 6
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 claims description 6
- 230000008878 coupling Effects 0.000 claims description 5
- 238000010168 coupling process Methods 0.000 claims description 5
- 238000005859 coupling reaction Methods 0.000 claims description 5
- 239000008367 deionised water Substances 0.000 claims description 5
- 229910021641 deionized water Inorganic materials 0.000 claims description 5
- 238000001035 drying Methods 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 claims description 5
- 239000000243 solution Substances 0.000 claims description 5
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 claims description 4
- 239000002202 Polyethylene glycol Substances 0.000 claims description 4
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 claims description 4
- 239000007822 coupling agent Substances 0.000 claims description 4
- 238000004945 emulsification Methods 0.000 claims description 4
- 239000012628 flowing agent Substances 0.000 claims description 4
- 229910021485 fumed silica Inorganic materials 0.000 claims description 4
- 230000000977 initiatory effect Effects 0.000 claims description 4
- 238000002955 isolation Methods 0.000 claims description 4
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 4
- 229920001223 polyethylene glycol Polymers 0.000 claims description 4
- 229920001296 polysiloxane Polymers 0.000 claims description 4
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 4
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 4
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 4
- 230000035484 reaction time Effects 0.000 claims description 4
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 claims description 4
- 235000019982 sodium hexametaphosphate Nutrition 0.000 claims description 4
- 239000007921 spray Substances 0.000 claims description 4
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 claims description 4
- 229920000877 Melamine resin Polymers 0.000 claims description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 3
- 229910021543 Nickel dioxide Inorganic materials 0.000 claims description 3
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 3
- 239000011230 binding agent Substances 0.000 claims description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 3
- 239000003638 chemical reducing agent Substances 0.000 claims description 3
- 239000011248 coating agent Substances 0.000 claims description 3
- 238000000576 coating method Methods 0.000 claims description 3
- 239000013530 defoamer Substances 0.000 claims description 3
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical group [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 claims description 3
- 235000019359 magnesium stearate Nutrition 0.000 claims description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 3
- 239000002480 mineral oil Substances 0.000 claims description 3
- 235000010446 mineral oil Nutrition 0.000 claims description 3
- MRHPUNCYMXRSMA-UHFFFAOYSA-N nickel(2+) oxygen(2-) Chemical compound [O--].[O--].[Ni++] MRHPUNCYMXRSMA-UHFFFAOYSA-N 0.000 claims description 3
- 239000012875 nonionic emulsifier Substances 0.000 claims description 3
- 150000002894 organic compounds Chemical class 0.000 claims description 3
- 229920000570 polyether Polymers 0.000 claims description 3
- 238000006479 redox reaction Methods 0.000 claims description 3
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 claims description 3
- 235000019832 sodium triphosphate Nutrition 0.000 claims description 3
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 claims description 3
- 239000005050 vinyl trichlorosilane Substances 0.000 claims description 3
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 claims description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 2
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
- NOZAQBYNLKNDRT-UHFFFAOYSA-N [diacetyloxy(ethenyl)silyl] acetate Chemical compound CC(=O)O[Si](OC(C)=O)(OC(C)=O)C=C NOZAQBYNLKNDRT-UHFFFAOYSA-N 0.000 claims description 2
- 230000009471 action Effects 0.000 claims description 2
- 229910001870 ammonium persulfate Inorganic materials 0.000 claims description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims description 2
- 235000013539 calcium stearate Nutrition 0.000 claims description 2
- 239000008116 calcium stearate Substances 0.000 claims description 2
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 claims description 2
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 claims description 2
- 239000011790 ferrous sulphate Substances 0.000 claims description 2
- 235000003891 ferrous sulphate Nutrition 0.000 claims description 2
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 claims description 2
- 229910000359 iron(II) sulfate Inorganic materials 0.000 claims description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
- 239000011976 maleic acid Substances 0.000 claims description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 2
- 239000012286 potassium permanganate Substances 0.000 claims description 2
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 claims description 2
- 239000000377 silicon dioxide Substances 0.000 claims description 2
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 claims description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 2
- DENFJSAFJTVPJR-UHFFFAOYSA-N triethoxy(ethyl)silane Chemical compound CCO[Si](CC)(OCC)OCC DENFJSAFJTVPJR-UHFFFAOYSA-N 0.000 claims description 2
- 239000001993 wax Substances 0.000 claims description 2
- 230000008901 benefit Effects 0.000 abstract description 8
- 238000001694 spray drying Methods 0.000 abstract description 6
- 238000002156 mixing Methods 0.000 abstract description 5
- 239000004566 building material Substances 0.000 abstract description 4
- 238000004140 cleaning Methods 0.000 abstract description 4
- 238000003786 synthesis reaction Methods 0.000 abstract description 4
- 230000004048 modification Effects 0.000 abstract description 3
- 238000012986 modification Methods 0.000 abstract description 3
- 239000003973 paint Substances 0.000 abstract description 3
- 230000006750 UV protection Effects 0.000 abstract 1
- 238000004383 yellowing Methods 0.000 abstract 1
- 239000004570 mortar (masonry) Substances 0.000 description 10
- 229920001971 elastomer Polymers 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 239000005060 rubber Substances 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- 238000006253 efflorescence Methods 0.000 description 6
- 230000002209 hydrophobic effect Effects 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 206010037844 rash Diseases 0.000 description 6
- 229920000800 acrylic rubber Polymers 0.000 description 5
- 239000004568 cement Substances 0.000 description 5
- 229920000058 polyacrylate Polymers 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 4
- 230000002776 aggregation Effects 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 238000005054 agglomeration Methods 0.000 description 3
- 239000011083 cement mortar Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000002861 polymer material Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 239000006004 Quartz sand Substances 0.000 description 2
- 229910018557 Si O Inorganic materials 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 229920003086 cellulose ether Polymers 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 239000004567 concrete Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- -1 polyol fatty acid ester Chemical class 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 241001391944 Commicarpus scandens Species 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 229920002522 Wood fibre Polymers 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000010000 carbonizing Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000033116 oxidation-reduction process Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 229920000056 polyoxyethylene ether Polymers 0.000 description 1
- 229940051841 polyoxyethylene ether Drugs 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 239000002025 wood fiber Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B40/00—Processes, in general, for influencing or modifying the properties of mortars, concrete or artificial stone compositions, e.g. their setting or hardening ability
- C04B40/0028—Aspects relating to the mixing step of the mortar preparation
- C04B40/0039—Premixtures of ingredients
- C04B40/0046—Premixtures of ingredients characterised by their processing, e.g. sequence of mixing the ingredients when preparing the premixtures
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/40—Compounds containing silicon, titanium or zirconium or other organo-metallic compounds; Organo-clays; Organo-inorganic complexes
- C04B24/42—Organo-silicon compounds
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B40/00—Processes, in general, for influencing or modifying the properties of mortars, concrete or artificial stone compositions, e.g. their setting or hardening ability
- C04B40/0028—Aspects relating to the mixing step of the mortar preparation
- C04B40/0039—Premixtures of ingredients
- C04B40/0042—Powdery mixtures
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/02—Acids; Metal salts or ammonium salts thereof, e.g. maleic acid or itaconic acid
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2103/00—Function or property of ingredients for mortars, concrete or artificial stone
- C04B2103/0045—Polymers chosen for their physico-chemical characteristics
- C04B2103/0057—Polymers chosen for their physico-chemical characteristics added as redispersable powders
Abstract
The invention belongs to the technical field of chemical synthesis in building materials, and particularly discloses a method for preparing redispersible latex powder by taking modified silicone-acrylate emulsion as a raw material, which comprises the steps of mixing an organosilicon monomer with an unsaturated bond and an acrylic monomer with an auxiliary agent, synthesizing the silicone-acrylate emulsion by a core-shell wrapping modification polymerization process, and preparing the redispersible latex powder by taking the silicone-acrylate emulsion as a base and performing spray drying The paint has the advantages of ultraviolet resistance, yellowing resistance, stain resistance, self-cleaning property, more excellent surface in building materials and wide application prospect.
Description
Technical Field
The invention belongs to the technical field of chemical synthesis in building materials, and particularly relates to a method for preparing redispersible latex powder by using modified silicone-acrylic emulsion as a raw material.
Background
With the development of chemical synthesis process and building materials, the application of special powder high molecular polymer is more and more extensive, and the high molecular polymer redispersible latex powder is needed in aspects related to national life, such as building mortar, cement concrete and building coating. The common redispersible latex powder is applied to cement mortar and paint, and can improve the cohesive force and cohesion of materials, improve the flexibility of the materials, improve the deformation capacity and the like. The production technology of four common redispersible latex powders on the market, such as vinyl acetate and ethylene copolymerized (VAE rubber powder), styrene and acrylic acid copolymerized (styrene-acrylic rubber powder), butyl acrylate copolymerized (styrene-butadiene rubber powder) and acrylate copolymerized (pure acrylic rubber powder), is mature, but the four polymers have the defects and shortcomings of performance. The VAE rubber powder has poor water resistance, is easy to hydrolyze in a humid environment, and has sharply reduced performance in a high-temperature or freeze-thaw environment. The three types of redispersible emulsion powder of styrene-butadiene rubber powder, styrene-acrylic rubber powder and pure acrylic rubber powder are limited by domestic production technology and foreign patents, core products and technologies are mastered in foreign enterprises, and the three types of emulsion powder have the problems of large brittleness, poor flexibility, poor deformation resistance, difficulty in resisting cement shrinkage, large water resistance and impermeability loss caused by large water absorption and the like, and are limited in market application. With the development of building industrialization and standardization, the demand for special mortars with special purposes, such as caulking mortar, joint mortar, sleeve grouting, pavement and dam spillway repair mortar, clear water mortar and the like, is increasingly high, the corresponding performance index needing high polymer is higher, the preparation and production process of the silicone-acrylic redispersible latex powder is not seen in patents and documents, and the silicone-acrylic redispersible latex powder disclosed by the invention has market advantages and also has great innovation and technical initiative advantages. The silicone-acrylate emulsion introduces an organosilicon monomer, so that the acrylic emulsion not only retains excellent film forming property, mechanical property and the like of the acrylic emulsion, but also has firm structure because the Si-O bond energy is far greater than C-C and C-O bonds, so that the acrylic emulsion has strong heat resistance, weather resistance, corrosion resistance and oxidation resistance, and simultaneously has self-cleaning property because the product has large molecular volume, low polarity and small solubility and is difficult to absorb water, so that the product has extremely strong hydrophobic and water repellent property, the adhesion of dust and pollutants to the surface of a material is reduced, and the performance requirement of the product in a harsh environment is met. Silicone-acrylic emulsion on the market is common, and if the common silicone-acrylic emulsion is directly sprayed and dried like EVA rubber powder, agglomeration is easy to occur, so that pipe blockage is caused. According to the invention, firstly, different emulsification systems are adopted to establish a core-shell coating reaction system in a silicone-acrylic emulsion synthesis process, so that an organic silicon monomer and an acrylic acid monomer can be uniformly and completely polymerized, which is equivalent to establishing a non-interfering reaction space, and the problem of difficult spray drying caused by high viscosity due to enrichment and adhesion of emulsion ions is prevented. In conclusion, the method is pioneering, overcomes great technical difficulty, and enables the prepared product to have innovation advantages and performance advantages.
Disclosure of Invention
The invention aims to provide a method for preparing redispersible latex powder by taking modified silicone-acrylate emulsion as a raw material, which aims to solve the problems of high brittleness, poor flexibility, poor deformation resistance, difficulty in resisting cement shrinkage, high water resistance and impermeability loss caused by high water absorption and the like of the conventional redispersible latex powder.
In order to achieve the purpose, the invention adopts the technical scheme that:
a method for preparing redispersible latex powder by taking modified silicone-acrylic emulsion as a raw material comprises the following steps:
(1) synthesizing modified silicone-acrylate emulsion: taking an organosilicon monomer with an unsaturated bond and an acrylic monomer as raw materials, and synthesizing a modified silicone-acrylate emulsion through a core-shell wrapping emulsification reaction, an initiation polymerization reaction and an oxidation reduction reaction under an auxiliary agent condition;
(2) preparing redispersible latex powder: taking the modified silicone-acrylic emulsion prepared in the step (1) as a raw material, respectively preparing a powder spraying mixed solution through an isolation mixed solution preparation stage, a colloid protection mixed solution preparation stage and a powder spraying mixed solution preparation stage under the action of a protective colloid, an isolating agent, a bubble eliminating agent, a dispersing agent, a flowing agent and an anti-plate caking agent, and drying the mixture into redispersible latex powder at a high temperature by adopting a rotary liquid spraying technology, wherein the specific reaction operation of the silicone-acrylic rubber powder production is as follows: 1. preparing an isolated mixed solution: fully and uniformly stirring the silicone-acrylic emulsion and the separant in a reaction container according to the proportion, and mixing for 0.5 h; 2. preparing a colloid protection mixed solution: mixing the prepared isolation mixed solution and the pre-dispersed protective colloid mixed solution according to a certain proportion to prepare colloid protective mixed solution; 3. preparing a powder spraying mixed solution: adding bubble eliminating agent, dispersant and flow agent into the colloid protection mixed solution, and stirring uniformly to obtain powder spraying mixed solution. Spraying the mixed solution in a rotary liquid spray drying tower, adding an anti-caking agent in the spraying process, wherein the rotating speed of a spraying head of the spraying tower is 22000-.
Further, in the step (1), the organosilicon monomer with an unsaturated bond is an unsaturated silane monomer coupling agent, the unsaturated acrylic monomer is an unsaturated acrylate monomer, the auxiliary agent is a polymeric emulsifier, a redox catalyst, an initiator, a foam inhibitor, a pH regulator, a surfactant and deionized water, and the dosage percentage of each raw material is 6-10% of the unsaturated silane coupling monomer, 35-45% of the unsaturated acrylate monomer, 0.5-1.2% of the polymeric emulsifier, 0.2-0.4% of the redox catalyst, 0.2-0.5% of the initiator, 0.2-0.6% of the foam inhibitor, 0.3-0.5% of the pH regulator, 0.1-0.3% of the surfactant and 40-60% of the deionized water.
Further, the unsaturated silane monomer coupling agent is at least one of vinyl trichlorosilane, vinyl trimethoxy silane, vinyl triacetoxy silane and ethyl triethoxy silane, the larger the molecule connected on a Si-O bond is, the lower the polarity is, the better the hydrophobic and hydrophobic performance is, the higher the stability is, and the better the performance is, and the unsaturated acrylate monomer is at least one of methyl methacrylate, hydroxyethyl acrylate, maleic acid, itaconic acid and n-butyl acrylate.
Furthermore, the polymeric emulsifier is a nonionic emulsifier with a hydrophilic-lipophilic balance value of 10-15, such as polyoxyethylene ether, polyol fatty acid ester and ethylene oxide block copolymer, and the emulsifier is a key step of silicone-acrylic emulsion polymerization reaction and directly influences the viscosity and molecular polarity of the polymeric emulsion. The nonionic emulsifier has higher emulsifying efficiency, is not easy to react with metal ions relative to other emulsifiers, is not easy to break emulsion when applied to a strong alkaline system, has better stability, can better protect silane bonds from being easily damaged in a core-shell reaction, has better dispersion and film-forming properties after being sprayed and dried, and effectively reduces the agglomeration phenomenon during spraying, the redox catalyst is at least one of nickel dioxide and potassium permanganate, the initiator is at least one of ammonium persulfate, potassium persulfate, azodiisobutyronitrile and sodium persulfate/ferrous sulfate, the initiator can efficiently cause the chain polymerization reaction of the polymerization reaction, so that the reaction is rapidly carried out, the foam inhibitor is a polyether defoamer, the pH regulator is a sodium hydroxide solution, and the surfactant is sodium dodecyl benzene sulfonate.
Further, the specific reaction operation of the silicone-acrylic emulsion in the step (1) is as follows: 1. pre-emulsion polymerization, core-shell reaction stage: putting unsaturated silane coupling monomer and polymeric emulsifier into a reactor heated by water bath according to a certain proportion, emulsifying for 0.5h at room temperature, then heating to 65-70 ℃, and reacting for 2h, wherein the main effects of the steps are that the polarity of the unsaturated silane coupling monomer is smaller, the solubility in water is small, the polymeric emulsifier is added to fully disperse the unsaturated silane coupling monomer in water to reach the hydrophilic-lipophilic balance value, and the silane group of the emulsifier is wrapped to form core-shell protection, and the group is not damaged in the subsequent reaction; 2. initiating polymerization stage: dropwise adding a pH regulator into the reacted solution, regulating the pH to 8-9, adding an unsaturated acrylic monomer according to a proportion, heating to 85 ℃, slowly dropwise adding an initiator, and continuously keeping the temperature of 85 ℃ for reaction for 1.5h after dropwise adding; 3. and in the oxidation-reduction stage, adding a redox catalyst, a surfactant and a foam inhibitor into the solution, heating to 95 ℃, oxidizing unreacted double bond monomers into saturated double bonds in the stage to enable reaction products to be more stable, wherein the reaction time in the stage is 1h, cooling the obtained polymer blue light emulsion (with the solid content of 45-55%) to room temperature for later use, and performing second-step spray drying to obtain the redispersible latex powder.
Furthermore, the dosage percentage of the raw materials in the step (2) is 60-75% of modified silicone-acrylate emulsion, 10-12% of protective colloid, 3-5% of separant, 2-4% of bubble remover, 1-1.5% of dispersant, 0.5-1.0% of flow agent and 6-23.5% of anti-plate binder.
Further, in the step (2), the protective colloid is at least one of a high molecular organic compound polyethylene glycol and polyvinylpyrrolidone, the protective colloid is a water-soluble high molecular linear organic compound, a common protective colloid of the redispersible latex powder is polyvinyl alcohol, but the common protective colloid is not easy to adopt in the silicone-acrylate emulsion powdering, compared with the polyvinyl alcohol, the water solubility of the polyethylene glycol and polyvinylpyrrolidone is better, the protective colloid can prevent the polymer from carbonizing caused by overhigh temperature in the spray drying process on one hand, on the other hand, the polymer has better hydrophilicity and film forming property after being powdered, the separant is at least one of calcium stearate, magnesium stearate and wax powder, the separant is a key step of powder spraying and drying, belongs to a hydrophobic compound, is not easy to be wetted by water, and can be dispersed in the silicone-acrylate emulsion under forced stirring, the emulsion has the advantages that the emulsion has a good granulation property only by playing an isolation role and reducing the acting force among emulsion particles to enable the emulsion particles to form independent single bodies which are not interfered with each other and preventing the aggregation and agglomeration phenomenon of spray drying, the bubble eliminating agent is at least one of a mineral oil defoaming agent and an organic silicon defoaming agent, the dispersing agent is at least one of sodium tripolyphosphate, sodium hexametaphosphate and naphthalenesulfonate, the flowing agent is at least one of melamine, naphthalenesulfonate and a carboxylic acid water reducing agent, and the anti-caking agent is at least one of fumed silica, precipitated silica, 1500-mesh talcum powder and 1200-mesh metakaolin.
Furthermore, the rotating speed of the spray head in the rotary liquid spraying technology is 28000-30000r/min, the temperature of the spray chamber is 140-160 ℃, compared with the rotating speed of the conventional redispersible latex powder, the rotating speed of the silicone-acrylic emulsion needs to be higher, and finer emulsion particles can be centrifuged during the rotary drying process, and the finer particle size is, the higher the corresponding rubber powder dispersibility, the film-forming property and the comprehensive performance are.
The invention has the advantages that: the invention overcomes the double technical problems of the silicon-acrylic emulsion powder spraying and drying compared with the traditional powder spraying technology of redispersible milk, and belongs to the initiative technology in China. The silicone-acrylate redispersible latex powder prepared by the invention is applied to building mortar, concrete and paint, and can better improve the comprehensive properties of products such as heat resistance, freeze-thaw resistance, water resistance, permeability resistance, stain resistance, self-cleaning property and the like.
Detailed Description
Example one
The selection and preparation process of the silicone-acrylic emulsion No. 1 sample polymer material are shown in Table 1 (the specific process is the reaction process of the silicone-acrylic emulsion)
TABLE 1
Composition of | Percentage of use |
Vinyl trichlorosilane (CH2 ═ CHSiCl3) | 8.0% |
Methyl Methacrylate (MMA) | 35% |
Polyol fatty acid esters | 0.8% |
Nickel dioxide | 0.3% |
Azobisisobutyronitrile | 0.3% |
Polyether defoaming agent | 0.4% |
Sodium hydroxide solution | 0.45% |
Sodium dodecyl benzene sulfonate | 0.22% |
Deionized water | 54.53% |
The selection and preparation process of sample No. 1 of the silicone-acrylate re-dispersible latex powder are shown in Table 2 (the reaction process of the silicone-acrylate re-dispersible latex powder is shown in detail)
TABLE 2
Composition of | Percentage of use |
Silicone acrylic emulsion No. 1 | 70% |
Polyethylene glycol (molecular weight 15000) | 11% |
Magnesium stearate | 3.5% |
Silicone defoaming agent | 3% |
Sodium hexametaphosphate | 1.2% |
Carboxylic acid water reducing agent | 0.8% |
Fumed silica | 10.5% |
Example two
The selection and preparation process of the silicone-acrylic emulsion No. 2 sample polymer material are shown in Table 3 (the specific process is the reaction process of the silicone-acrylic emulsion)
TABLE 3
The selection and preparation process of sample No. 2 of the silicone-acrylate re-dispersible latex powder are shown in Table 4 (the reaction process of the silicone-acrylate re-dispersible latex powder is shown in detail)
TABLE 4
EXAMPLE III
The selection and preparation process of the silicone-acrylic emulsion No. 3 sample polymer material are shown in Table 5 (the specific process is the reaction process of the silicone-acrylic emulsion)
TABLE 5
The selection and preparation process of sample No. 3 of the silicone-acrylate re-dispersible latex powder are shown in Table 6 (the reaction process of the silicone-acrylate re-dispersible latex powder is shown in detail)
TABLE 6
Composition of | Percentage of use |
Silicone acrylic emulsion No. 3 | 75% |
Polyvinylpyrrolidone | 10% |
Wax powder | 3.0% |
Mixing mineral oil defoaming agent and organosilicon defoaming agent in a ratio of 1:1 | 4% |
Mixing sodium tripolyphosphate and sodium hexametaphosphate in a ratio of 1:2 | 1.0% |
Melamine mixed with naphthalene sulfonate 1:2 | 1.0% |
Fumed silica is 1:1 mixed with 1200 mesh metakaolin | 6.0% |
The redispersible latex powder produced in the above examples 1-3 according to the production process is a silicone-acrylic redispersible latex powder.
The silicon-acrylic re-dispersible latex powder obtained by the production is prepared into a ceramic tile binder (PO42.5 cement: 35%, 40-140 mesh quartz sand: 63.2%, 10 ten thousand viscosity cellulose ether: 0.3%, re-dispersible latex powder 1.5%, and is compared with high-end re-dispersible latex powder in the market (comparison sample 1: ternary copolymerization hydrophobic rubber powder, comparison sample 2: pure acrylic rubber powder) for forming, and the product performance is tested according to ceramic wall and floor tile adhesive (JG/T547-.
TABLE 7
The test result of the tile adhesive shows that compared with the traditional imported high-end redispersible latex powder, the silicon-acrylic redispersible latex powder has higher cohesive force, better waterproof and impervious effect, and more excellent heat resistance and freeze-thaw resistance when being applied to cement mortar.
The silica-acrylic redispersible latex powder obtained by the production is prepared into decorative mortar (PO42.5 white cement: 25%, metakaolin: 5.0%, 40-140 mesh quartz sand: 66.75%, defoamer: 0.2%, wood fiber 0.4%, 4 ten thousand viscosity cellulose ether: 0.15%, redispersible latex powder 2.5%, and is compared and formed with the market high-end redispersible latex powder (comparative sample 1: terpolymer hydrophobic rubber powder, comparative sample 2: pure acrylic rubber powder), and the product performance is tested according to wall facing mortar (JG/T1024-shaped 2019), and the specific test result is shown in Table 8.
TABLE 8
Example 1 | Example 2 | Example 3 | Comparative sample 1 | Comparative sample 2 | |
240min Water absorption/g | 1.12 | 1.15 | 1.14 | 10.24 | 9.25 |
Resistance to efflorescence | No efflorescence | No efflorescence | No efflorescence | Large area efflorescence | Large area efflorescence |
Stain resistance | Stage 2 | Stage 2 | Stage 2 | Level 0 | Level 0 |
Weather resistance | Level 1 | Level 1 | Level 1 | Powder falling and color changing | Powder falling and color changing |
From the test results of the decorative mortar, compared with the traditional imported high-end redispersible latex powder, the silicone-acrylic redispersible latex powder has the advantages of lower water absorption, better alkali resistance, stain resistance, self-cleaning property, lasting weather resistance and the like when being applied to cement mortar.
The above description is only a preferred embodiment of the present invention and is not intended to limit the present invention, and various modifications and changes may be made by those skilled in the art. Any modification, equivalent replacement, or improvement made within the spirit and principle of the present invention should be included in the protection scope of the present invention.
Claims (8)
1. A method for preparing redispersible latex powder by taking modified silicone-acrylic emulsion as a raw material is characterized by comprising the following steps:
(1) synthesizing modified silicone-acrylate emulsion: taking an organosilicon monomer with an unsaturated bond and an acrylic monomer as raw materials, and synthesizing a modified silicone-acrylate emulsion through a core-shell wrapping emulsification reaction, an initiation polymerization reaction and an oxidation reduction reaction under an auxiliary agent condition;
(2) preparing redispersible latex powder: taking the modified silicone-acrylic emulsion prepared in the step (1) as a raw material, respectively preparing a spraying mixed solution through an isolation mixed solution preparation stage, a colloid protection mixed solution preparation stage and a spraying mixed solution preparation stage under the action of a protective colloid, an isolating agent, a bubble eliminating agent, a dispersing agent, a flowing agent and an anti-plate caking agent, and drying at a high temperature by adopting a rotary liquid spraying technology to obtain the redispersible emulsion powder.
2. The method for preparing the redispersible latex powder by using the modified silicone-acrylic emulsion as the raw material as claimed in claim 1, wherein: the organosilicon monomer of the unsaturated bond in the step (1) is an unsaturated silane monomer coupling agent, the unsaturated acrylic monomer is an unsaturated acrylate monomer, the auxiliary agent is a polymeric emulsifier, a redox catalyst, an initiator, a foam inhibitor, a pH regulator, a surfactant and deionized water, and the dosage percentage of the raw materials is 6-10% of the unsaturated silane coupling monomer, 35-45% of the unsaturated acrylate monomer, 0.5-1.2% of the polymeric emulsifier, 0.2-0.4% of the redox catalyst, 0.2-0.5% of the initiator, 0.2-0.6% of the foam inhibitor, 0.3-0.5% of the pH regulator, 0.1-0.3% of the surfactant and 40-60% of the deionized water.
3. The method for preparing the redispersible latex powder by using the modified silicone-acrylic emulsion as the raw material as claimed in claim 2, wherein: the unsaturated silane monomer coupling agent is at least one of vinyl trichlorosilane, vinyl trimethoxy silane, vinyl triacetoxy silane and ethyl triethoxy silane, and the unsaturated acrylate monomer is at least one of methyl methacrylate, hydroxyethyl acrylate, maleic acid, itaconic acid and n-butyl acrylate.
4. The method for preparing the redispersible latex powder by using the modified silicone-acrylic emulsion as the raw material as claimed in claim 3, wherein: the polymerization emulsifier is a nonionic emulsifier with a hydrophilic-lipophilic balance value of 10-15, the redox catalyst is at least one of nickel dioxide and potassium permanganate, the initiator is at least one of ammonium persulfate, potassium persulfate, azodiisobutyronitrile and sodium persulfate/ferrous sulfate, the foam inhibitor is a polyether defoamer, the pH regulator is a sodium hydroxide solution, and the surfactant is sodium dodecyl benzene sulfonate.
5. The method for preparing the redispersible latex powder by using the modified silicone-acrylic emulsion as the raw material as claimed in claim 4, wherein: in the step (1), the core-shell coating emulsification reaction temperature is 65-70 ℃, the reaction time is 2 hours, the polymerization initiation reaction temperature is 85 ℃, the reaction time is 1.5 hours, the temperature of the redox reaction is 95 ℃, and the reaction time is 2 hours, and all the reactions are water bath reactions.
6. The method for preparing the redispersible latex powder by using the modified silicone-acrylic emulsion as the raw material as claimed in claim 5, wherein: in the step (2), the dosage percentage of the raw materials is 60-75% of modified silicone-acrylate emulsion, 10-12% of protective colloid, 3-5% of separant, 2-4% of bubble remover, 1-1.5% of dispersant, 0.5-1.0% of flow agent and 6-23.5% of anti-plate binder.
7. The method for preparing the redispersible latex powder by using the modified silicone-acrylic emulsion as the raw material as claimed in claim 6, wherein: the protective colloid is at least one of high molecular organic compounds polyethylene glycol and polyvinylpyrrolidone, the isolating agent is at least one of calcium stearate, magnesium stearate and wax powder, the bubble eliminating agent is at least one of mineral oil defoaming agent and silicone defoaming agent, the dispersing agent is at least one of sodium tripolyphosphate, sodium hexametaphosphate and naphthalenesulfonate, the flowing agent is at least one of melamine, naphthalenesulfonate and carboxylic acid water reducing agent, and the anti-hardening agent is at least one of fumed silica, precipitated silica, 1500-mesh talcum powder and 1200-mesh metakaolin.
8. The method for preparing the redispersible latex powder by using the modified silicone-acrylic emulsion as the raw material as claimed in claim 7, wherein: the rotating speed of the spray head in the rotary liquid spraying technology is 28000-30000r/min, and the temperature of the spray chamber is 140-160 ℃.
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