CN113683948B - Production method of anti-wind-crack impact-resistant real stone paint - Google Patents
Production method of anti-wind-crack impact-resistant real stone paint Download PDFInfo
- Publication number
- CN113683948B CN113683948B CN202110870783.9A CN202110870783A CN113683948B CN 113683948 B CN113683948 B CN 113683948B CN 202110870783 A CN202110870783 A CN 202110870783A CN 113683948 B CN113683948 B CN 113683948B
- Authority
- CN
- China
- Prior art keywords
- paint
- sand
- wind
- resistance
- natural stone
- 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.)
- Expired - Fee Related
Links
- 239000003973 paint Substances 0.000 title claims abstract description 66
- 239000004575 stone Substances 0.000 title claims abstract description 30
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 13
- 239000004576 sand Substances 0.000 claims abstract description 45
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 51
- 239000004816 latex Substances 0.000 claims description 26
- 229920000126 latex Polymers 0.000 claims description 26
- 229920001084 poly(chloroprene) Polymers 0.000 claims description 24
- 238000002156 mixing Methods 0.000 claims description 23
- 239000004814 polyurethane Substances 0.000 claims description 23
- 229920002635 polyurethane Polymers 0.000 claims description 23
- 239000000839 emulsion Substances 0.000 claims description 20
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 18
- 239000002270 dispersing agent Substances 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 15
- 239000002002 slurry Substances 0.000 claims description 14
- 239000002518 antifoaming agent Substances 0.000 claims description 13
- 239000003431 cross linking reagent Substances 0.000 claims description 13
- 238000003756 stirring Methods 0.000 claims description 12
- 239000002245 particle Substances 0.000 claims description 11
- 239000007787 solid Substances 0.000 claims description 10
- 239000004579 marble Substances 0.000 claims description 9
- 238000004381 surface treatment Methods 0.000 claims description 8
- IBLKWZIFZMJLFL-UHFFFAOYSA-N 1-phenoxypropan-2-ol Chemical compound CC(O)COC1=CC=CC=C1 IBLKWZIFZMJLFL-UHFFFAOYSA-N 0.000 claims description 7
- 239000006004 Quartz sand Substances 0.000 claims description 7
- 238000004898 kneading Methods 0.000 claims description 6
- -1 N' -diethyl thiourea Chemical compound 0.000 claims description 5
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 5
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims description 5
- 241001426407 Umbrina coroides Species 0.000 claims description 4
- 239000013530 defoamer Substances 0.000 claims description 4
- 238000007599 discharging Methods 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- JAEZSIYNWDWMMN-UHFFFAOYSA-N 1,1,3-trimethylthiourea Chemical compound CNC(=S)N(C)C JAEZSIYNWDWMMN-UHFFFAOYSA-N 0.000 claims description 3
- PDQAZBWRQCGBEV-UHFFFAOYSA-N Ethylenethiourea Chemical compound S=C1NCCN1 PDQAZBWRQCGBEV-UHFFFAOYSA-N 0.000 claims description 3
- 125000002091 cationic group Chemical group 0.000 claims description 2
- 229920001296 polysiloxane Polymers 0.000 claims 2
- PKDCQJMRWCHQOH-UHFFFAOYSA-N triethoxysilicon Chemical compound CCO[Si](OCC)OCC PKDCQJMRWCHQOH-UHFFFAOYSA-N 0.000 claims 2
- 230000000694 effects Effects 0.000 abstract description 12
- 230000008901 benefit Effects 0.000 abstract description 4
- 238000012824 chemical production Methods 0.000 abstract description 2
- 230000014759 maintenance of location Effects 0.000 abstract 1
- 238000012360 testing method Methods 0.000 description 37
- 238000000576 coating method Methods 0.000 description 33
- 239000011248 coating agent Substances 0.000 description 31
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 20
- 238000005336 cracking Methods 0.000 description 15
- 230000008859 change Effects 0.000 description 14
- 239000011259 mixed solution Substances 0.000 description 12
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- 238000000034 method Methods 0.000 description 8
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 7
- 238000001035 drying Methods 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 238000005054 agglomeration Methods 0.000 description 6
- 230000002776 aggregation Effects 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 238000003860 storage Methods 0.000 description 6
- 230000035882 stress Effects 0.000 description 6
- 239000002585 base Substances 0.000 description 5
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- 230000032683 aging Effects 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- 238000002791 soaking Methods 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 3
- 239000004342 Benzoyl peroxide Substances 0.000 description 3
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 3
- 239000005058 Isophorone diisocyanate Substances 0.000 description 3
- 241000533950 Leucojum Species 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 235000019400 benzoyl peroxide Nutrition 0.000 description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 230000006837 decompression Effects 0.000 description 2
- 238000005034 decoration Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- 239000010438 granite Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 230000033001 locomotion Effects 0.000 description 2
- 239000004570 mortar (masonry) Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 238000010008 shearing Methods 0.000 description 2
- WBQTXTBONIWRGK-UHFFFAOYSA-N sodium;propan-2-olate Chemical compound [Na+].CC(C)[O-] WBQTXTBONIWRGK-UHFFFAOYSA-N 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- FBBATURSCRIBHN-UHFFFAOYSA-N triethoxy-[3-(3-triethoxysilylpropyldisulfanyl)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCSSCCC[Si](OCC)(OCC)OCC FBBATURSCRIBHN-UHFFFAOYSA-N 0.000 description 2
- VTHOKNTVYKTUPI-UHFFFAOYSA-N triethoxy-[3-(3-triethoxysilylpropyltetrasulfanyl)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCSSSSCCC[Si](OCC)(OCC)OCC VTHOKNTVYKTUPI-UHFFFAOYSA-N 0.000 description 2
- FLVIGYVXZHLUHP-UHFFFAOYSA-N N,N'-diethylthiourea Chemical compound CCNC(=S)NCC FLVIGYVXZHLUHP-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000011083 cement mortar Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000013016 damping Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000005338 heat storage Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/08—Anti-corrosive paints
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
- C09D7/62—Additives non-macromolecular inorganic modified by treatment with other compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Paints Or Removers (AREA)
Abstract
The invention discloses a production method of a weather-resistant and impact-resistant natural stone paint, which belongs to the technical field of chemical production, wherein the natural stone paint produced by the production method disclosed by the invention is prepared from natural colored sand, has the advantages of good weather resistance, color retention, weather resistance, good flexibility and collision resistance, has good decorative effect and real stone texture, adopts natural stone colored sand to ensure the weather resistance of the natural stone paint, does not need a complex structural form, is constructed according to the general natural stone paint, has good wind crack resistance and impact resistance, meets the use requirements of indoor and outdoor natural stone paints in physicochemical properties, meets the roughness and the use performance of the surface of the natural stone paint, has good wind crack resistance and impact resistance, is suitable for the geographical environments of strong wind, low pressure and wind and sand, has long service life, and solves the application problem that the traditional natural stone paint cannot be applied to regions with windy and sandy climatic environment conditions.
Description
Technical Field
The invention belongs to the technical field of chemical production, and particularly relates to a production method of a wind crack resistant and impact resistant stone-like paint.
Background
The stone-like paint has a decorative effect similar to that of marble and granite. It is mainly made up by using natural stone powder with various colours, and can be used for external wall of building to produce imitation stone effect, so that it is also called liquid stone. The coating has good water resistance, stable coloration, no blushing and no chromatic aberration. However, at present, the real stone paint coating cracks in the northwest areas or plateau areas of strong wind and low pressure in windy weather, the coating becomes loose, and the cracks gradually grow after a long time, so that the service life of the real stone paint is greatly shortened. Wind fractures are the "induced" sites of median reticular fractures. Usually, the induction is performed at one place, and the full disk can be lost. In fact, the common real stone paint can obtain good application effect in plain basins and even mountainous regions, and the wind crack defect is not obvious. However, in the northwest area or plateau area with frequent strong winds, cracking is frequent, the performance looks sharp and is changed into a chicken-rib-type appearance wall decoration material. The reason is that the products on the market do not have good wind crack and impact resistance, and related technologies and production processes are not available. The general stone-like paint has not been solved properly because of the wind crack of tearing form caused by stress concentration. Along with the improvement of the decoration requirements of people on internal and external wall coatings, natural real stone paint is increasingly popular with people due to the unique appearance and performance, and the real stone paint which is similar to the appearance of natural stone materials such as natural granite, marble and the like is proposed in a plurality of high-grade houses, courtyards and even high-rise buildings, and is required to have stronger hardness, water resistance, aging resistance and the like in the aspect of performance. Chinese patent CN206873814U discloses a paint block of an anti-cracking real stone paint, which realizes anti-cracking through a structure, the paint positioning layer and the first glass fiber net realize reliable connection between the paint surface layer and the substrate layer, and the integral molding among the second glass fiber net, the paint positioning layer and the back paint layer realizes reliable connection between the back paint layer, but the structure and the process are complex, the cost is higher, and the applicability is not strong. The development of a production method of a wind crack and impact resistant real stone paint is urgently needed by the technical personnel in the field.
Disclosure of Invention
Aiming at the problems, the invention aims to provide a production method of a wind-crack-resistant and impact-resistant real stone paint.
The invention is realized by the following technical scheme:
a production method of a wind-crack-resistant and impact-resistant real stone paint comprises the following steps:
the method comprises the following steps of firstly, surface treatment of colored sand: feeding the color sand into a drum mixer, adding a cross-linking agent, and discharging after the treatment is finished;
further, the dispersant in the first step is a mixture of bis- [ gamma- (triethoxysilyl) propyl ] tetrasulfide and bis- [ gamma- (triethoxysilyl) propyl ] -disulfide in a weight ratio of 2: 1, the rotating speed of a rotary drum mixer in the first step is 15-20r/min, the rotating speed of a forced stirring paddle is 800-950r/min, and the cross-linking agent accounts for 2-3% of the color sand.
Si-69, si-75, also called: a-1289, Z-6940 and the like, which have silane active terminals and active sulfur, can perform surface treatment on the colored sand and simultaneously have active sulfur capable of performing a crosslinking function.
Step two, preparation of blended paint slurry: adding neoprene latex into a kneader, adding the polyurethane acrylate emulsion, and uniformly mixing;
the blending has the dual advantages of both neoprene latex and polyurethane, namely water resistance, permeability resistance, aging resistance, no toxicity, strong base layer deformation resistance and the like, and is cold work construction with convenient operation. The solubility parameters are close, the impact is buffered by the damping effect, and the wind crack resistance is improved;
step three, mixing the paint slurry: and uniformly mixing the blended paint slurry, the propylene glycol phenyl ether, the accelerator, the defoamer, the dispersant and the treated color sand drum mixer to obtain the wind crack resistant and impact resistant stone-like paint.
The discourse, weilinggong records that "the worker wants to improve his or her performance, and must first benefit his or her device. The V-shaped drum mixer is used for surface treatment and paint mixing, so that gravity settling is avoided, the mixing effect can be greatly improved, and a curved baffle is additionally arranged on the inner wall of the mixing chamber to guide materials to move from one end of the mixing chamber to the other end of the mixing chamber during rotation of the mixing chamber, so that the possibility of mutual contact of the materials is increased.
And further, uniformly mixing the colored sand in the third step with a drum mixer according to the weight ratio of 10-20 meshes of snowflake white sand to 20-40 meshes of marble to 40: 20-40 meshes of quartz sand to 40-80 meshes of 80: 40-80 meshes of ocular iron ore to 5: 80-120 meshes of floor yellow 2, wherein the rotating speed of the drum mixer is 15-20r/min, and the rotating speed of a forced stirring paddle is 800-950r/min.
Actually, the color sand used in the invention is natural compound color sand, which is mixed by different grading particle sizes. The stone-like paint sand with different grain sizes and reasonable grading can be mutually supplemented to avoid the stress concentration in the gaps during spraying or coating. But does not achieve good application effect in practical application. In the past, people widely use a high-speed mixer to mix in the preparation of coatings, but the real stone paint sand with different particle sizes can be settled due to the gravity, the expected target of gradation is contradictory, more gaps caused by uneven particle size distribution are formed, and the wind crack resistance and impact resistance are greatly reduced, so that the method is suitable for the contrary.
Further, the weight proportion of the polychloroprene latex in the step is 15-20%, the rotation speed of a main shaft of a kneading machine is 20-25r/min, the auxiliary shaft of the kneading machine is 10-15r/min, the steam pressure is 0.4-0.45MPa, and the kneading time is 5-10 minutes.
The V-blender is composed of two cylinders welded together in a V-shape, the shape of the container being asymmetrical with respect to the axis. The powder and granular material are continuously and repeatedly alternated, divided and combined in the inclined cylinder due to the rotary motion. The materials are randomly transferred from one area to another area, meanwhile, the sand particles slide to be overlapped for a plurality of times in space, and the sand particles are continuously distributed on the newly generated surface, so that the shearing and the diffusion movement are repeatedly carried out, and the uniform mixing is really achieved, but not the uneven distribution of the grading particle size caused by gravity sedimentation only through rotation.
Furthermore, the dispersant in the third step is a mixture of zinc stearate and triethanolamine in a weight ratio of 2: 1.
The dispersant, zinc stearate and triethanolamine can also be used as an active agent for latex, can be directly added into the latex, can neutralize the acidity of pottery clay, increases the air tightness and tear resistance of products, and has the function of the dispersant.
Further, the defoaming agent in the third step is one of an organic silicon defoaming agent TEGO 825 and an organic silicon defoaming agent TEGO 8030.
Further, the accelerator in the third step is one or more of ethylene thiourea, N' -diethyl thiourea, sodium isopropoxide, trimethyl thiourea and acetaldehyde ammonia (1-aminoethanol).
And further, the third step is that the paint slurry is mixed by weight parts of 150 to 250, 5 to 15 parts of propylene glycol phenyl ether, 3 to 5 parts of an accelerator, 1 to 3 parts of a defoaming agent, 7 to 9 parts of a dispersing agent and 1000 to 1100 parts of processed color sand.
The polyurethane emulsion is prepared by assembling a reaction kettle, a stirrer and a heating pot, adding n-butyl alcohol into the reaction kettle, heating to 95 ℃, dissolving 0.2-0.5 phr of benzoyl peroxide into a mixed solution of 34-41phr of methyl methacrylate, 15-24phr of hydroxyethyl acrylate, 5-10phr of acrylic acid, 12-14phr of butyl acrylate and 0.5-2phr of dodecyl mercaptan, dropwise adding the mixed solution into a flask, dropwise adding the mixed solution for 2-4h, controlling the temperature to be 95 ℃, dropwise adding the mixed solution, keeping the temperature for 0.5-1h, cooling to below 60 ℃, dropwise adding a partial solvent under reduced pressure, dropwise adding 15-12 parts of isophorone diisocyanate, uniformly stirring, standing for 20-30min, adding triethylamine, adjusting the pH value to 7.5-8.0, adding water, and diluting to a solid content of 20-25%, thus obtaining the polyurethane acrylate emulsion.
Further, the neoprene latex is cationic neoprene latex with the pH value of 11-12, the solid content of 48-50% and the latex particle size of 50-190 mm, and the solid content of the polyurethane acrylate emulsion is 20-25%.
The mixed paint slurry has good air tightness, water resistance, adhesion, weather resistance, chemical resistance and other performances, and avoids the penetration of wind and air to a certain extent.
One of the technical keys of the preparation method of the impact-resistant interpenetrating network anticorrosive coating is that neoprene latex and polyurethane acrylate emulsion are utilized, neoprene components and polyurethane have similar solubility parameters and similar polarities, and can be matched with each other and mutually promoted, the surface interface energy of the colored sand is reduced because the surface of the colored sand is modified by a cross-linking agent, and the cross-linking agent can promote the neoprene latex to be cross-linked with the polyurethane acrylate emulsion to form a uniform cross-linked network structure, so that the coating has higher impact strength and good comprehensive performance of wind crack resistance.
The invention has the beneficial effects that:
the invention uses neoprene latex and polyurethane acrylate emulsion to blend, and treats the surface of color sand through cross-linking agent, wherein neoprene particles play a role of stress concentration point, the existence of neoprene elastic phase enables the stressed material to generate deformation processes, energy absorption during fracture can be obviously improved, cross-linked glassy polymer can be increased to yield by a shearing mechanism, fatigue damage and cracking of real stone paint under long-time strong wind blow can be prevented, and expansion and extension of tiny cracks can be inhibited. Particularly, on the basis of the second-size stacking, the effect of adding specularite is increased on the basis, the specularite is probably derived from a lamellar structure of the specularite, a grid is formed among the gravels, the filler and the matrix resin are combined into a whole through an interface area, the stress is transmitted through the grid, a complete bonding surface is provided, the stress can be uniformly transmitted, a color sand interface subjected to surface treatment by the cross-linking agent is subjected to surface treatment, crack expansion is prevented and stress concentration is slowed down under the organic cooperation of polyurethane acrylate and neoprene, namely, a relaxation effect is achieved, and the effects of impact resistance, large wind blowing resistance and wind cracking resistance are further achieved.
Compared with the prior art, the invention has the following advantages:
the stone-like paint disclosed by the invention has a good decorative effect, has the texture of stone-like color sand, is good in weather resistance, ensures the weather-resistant effect of the stone-like paint, does not need a complex structural form, is constructed according to the general stone-like paint, has good anti-cracking and impact-resistant properties, meets the requirements of water resistance, acid resistance, good adhesive force and hard and impact-resistant coating film on the aspect of physical and chemical properties, meets the rough texture and the service performance of the surface of the stone-like paint, has good anti-cracking and impact-resistant properties, is suitable for being used in geographical environments with strong wind, low pressure and wind sand, and has a long service life.
Detailed Description
The invention is illustrated by the following specific examples, which are not intended to be limiting.
Example 1
Firstly, surface treatment of colored sand: sending the color sand into a drum mixer, adding a cross-linking agent, discharging after the treatment is finished, wherein the dispersant in the first step is prepared by uniformly mixing a mixture of bis- [ gamma- (triethoxysilicacid) propyl ] tetrasulfide and bis- [ gamma- (triethoxysilicacid) propyl ] -disulfide with the weight ratio of 2: 1, the rotating speed of the drum mixer is 20r/min, the rotating speed of a forced stirring paddle is 950r/min, the weight ratio of the cross-linking agent to the color sand is 3%, the weight ratio of the color sand to snowflake white sand of 10 to 20 to 40 to marble of 40 to quartz sand of 80 to 40 to 80 to iron ore of 5 to 80 to 120-mesh floor yellow 2 by the drum mixer; secondly, preparing the blended mill base: adding neoprene latex into a kneader, adding polyurethane acrylate emulsion, and uniformly mixing, wherein the weight proportion of the neoprene latex in the polyurethane acrylate emulsion is 20%, the rotating speed of a main shaft of the kneader is 25r/min, the auxiliary shaft of the kneader is 15r/min, the steam pressure is 0.45MPa, and the kneading time is 10 minutes; and finally, mixing the paint slurry: uniformly mixing the blended paint slurry, propylene glycol phenyl ether, an accelerant, an antifoaming agent, a dispersing agent and a treated color sand drum mixer, wherein the rotating speed of the drum mixer is 20r/min, the rotating speed of a forced stirring paddle is 950r/min, so as to obtain the wind crack resistant and impact resistant real stone paint, wherein the blended paint slurry comprises 250 parts by weight of the blended paint slurry, 15 parts by weight of the propylene glycol phenyl ether, 5 parts by weight of an accelerant ethylene thiourea, 5 parts by weight of the accelerant, 3 parts by weight of the antifoaming agent, 9 parts by weight of the dispersing agent and 1100 parts by weight of treated color sand, the dispersing agent is a mixture of zinc stearate and triethanolamine in a weight ratio of 2: 1, the antifoaming agent is an organic silicon antifoaming agent TEGO neoprene latex which is long-life CRL50LK cation neoprene latex, the pH value of which is 11, the solid content of which is 48%, the particle size of the latex is 50-190 mm, and the solid content of the polyurethane acrylate emulsion is 20%. The polyurethane emulsion is characterized in that a reaction kettle, a stirrer and a heating pot are assembled, n-butanol is added into the reaction kettle and heated to 95 ℃, then 0.5phr of benzoyl peroxide is dissolved in a mixed solution of 41phr of methyl methacrylate, 24phr of hydroxyethyl acrylate, 10phr of acrylic acid, 14phr of butyl acrylate and 2phr of dodecanethiol, the mixed solution is dripped into a flask for 4 hours, the temperature is controlled to 95 ℃, the temperature is kept for 1 hour and reduced to below 60 ℃, partial solvent is removed by dripping thermal decompression, 12 parts of isophorone diisocyanate are dripped, the mixed solution is stirred uniformly and then stands for 30 minutes, triethylamine is added, the pH value is adjusted to 8.0, the mixed solution is diluted to 20% of solid content by adding water, and XH-5008H with the weight of the water is added, so that the polyurethane acrylate emulsion is obtained. Snow white sand Susonggao river, silicou quartz sand Fengyang Temple, floor Huanghu Beibei Tieshan, xuanlang Marble sand Anqingsha, and Wuhu Dengchang specularite.
The product performance is as follows: no caking is generated after stirring in a container, the paint is in a uniform state and is not difficult to spray in construction, after 3 times of tests of freeze-thaw cycle storage stability of the paint, no caking, agglomeration and composition change exist, after 1 month of test of paint thermal storage stability, no caking, mildewing, agglomeration and composition change exist, the initial drying and wind crack resistance time (surface drying) is short, and no cracks exist within 3 hours; the water-resistant 96h coating has no bulging, cracking and peeling, compared with the part which is not soaked, the color is allowed to slightly change, the alkali-resistant 96h coating has no bulging, cracking and peeling, compared with the part which is not soaked, the color is slightly changed; the impact-resistant coating has no cracks, peeling and obvious deformation; the standard state of the bonding strength is 0.74MPa, and the standard state is 0.58MPa after soaking; the coating with the artificial aging resistance of 500h has no bulging, cracking and peeling, the powdering is 0 grade, and the color change is less than 1 grade.
Example 2
Firstly, surface treatment of colored sand: feeding color sand into a drum mixer, adding a cross-linking agent, discharging after treatment is finished, wherein the dispersant in the first step is a mixture of bis- [ gamma- (triethoxysilyl) propyl ] tetrasulfide and bis- [ gamma- (triethoxysilyl) propyl ] -disulfide with the weight ratio of 2: 1, the rotating speed of the drum mixer is 15r/min, the rotating speed of a stirring paddle is forced to be 800r/min, the weight ratio of the cross-linking agent to the color sand is 2%, the color sand is 10 to 20 meshes of snowflake white sand, 20 to 20 meshes of marble, 40 to 20 meshes of marble, 80 to 40 meshes of quartz sand, 80 to 40 to 80 meshes of iron ocular ore, 5 to 80 to 120 meshes of floor yellow 2, and the mixture is uniformly mixed through the drum mixer, wherein the rotating speed of the drum mixer is 15r/min, and the rotating speed of the stirring paddle is forced to be 800r/min; secondly, preparing blended mill base: adding neoprene latex into a kneader, adding polyurethane acrylate emulsion, and uniformly mixing, wherein the weight proportion of the neoprene latex in the polyurethane acrylate emulsion is 15%, the rotating speed of a main shaft of the kneader is 20r/min, the auxiliary shaft of the kneader is 10r/min, the steam pressure is 0.4MPa, and the kneading time is 5 minutes; thirdly, mixing the paint slurry: uniformly mixing the blended paint paste, propylene glycol phenyl ether, an accelerator, an antifoaming agent, a dispersing agent and a treated color sand drum mixer to obtain the wind-crack-resistant and impact-resistant real stone paint, wherein the blended paint paste comprises 150 parts by weight, 5 parts by weight, 1000 parts by weight of accelerator N, N' -diethylthiourea, sodium isopropoxide, trimethylthiourea and acetaldehyde ammonia (1-aminoethanol), the dispersing agent comprises a mixture 3 of zinc stearate and triethanolamine in a weight ratio of 2: 1, the antifoaming agent is an organic silicon antifoaming agent TEGO 8030, neoprene latex is CRL50 cation neoprene latex with a pH value of 12, the solid content of 50%, the latex particle size is 50-190 mm, and the solid content of the polyurethane acrylate emulsion is 25%.
The polyurethane emulsion is characterized in that a reaction kettle, a stirrer and a heating pot are assembled, n-butanol is added into the reaction kettle and heated to 95 ℃, then 0.2phr of benzoyl peroxide is dissolved in a mixed solution of 34phr of methyl methacrylate, 15phr of hydroxyethyl acrylate, 5phr of acrylic acid, 12phr of butyl acrylate and 0.5phr of dodecanethiol, the mixed solution is dripped into a flask, the dripping time is 2, the temperature is controlled to be 95 ℃, the temperature is kept for 0.5H and reduced to be below 60 ℃ after the dripping is finished, partial solvent is removed by dripping thermal decompression, 12 parts of isophorone diisocyanate are dripped, the mixed solution is stirred uniformly and then stands for 20min, triethylamine is added, the pH value is adjusted to 8.0, water is added to dilute the mixed solution to 25%, and XH-5008H with the weight of 0.02% of water is added to obtain the polyurethane acrylate emulsion. Snow white sand dorong Liao river, silica valley quartz sand Fengyang Temple, floor Huanghu Beibei Tieshan, xuanlang Marble sand Anqingshao, and WU lake Mian Chang specularite.
The product performance is as follows: no caking is generated after stirring in a container, the paint is in a uniform state and is not difficult to spray in construction, after 3 times of tests of freeze-thaw cycle storage stability of the paint, no caking, agglomeration and composition change exist, after 1 month of test of paint thermal storage stability, no caking, mildewing, agglomeration and composition change exist, the initial drying and wind crack resistance time (surface drying) is short, and no cracks exist within 3 hours; the water resistance of the coating is 96h, the coating does not bulge, crack or peel, and the color is allowed to slightly change compared with the part which is not soaked; the alkali-resistant 96h coating has no bulging, cracking and peeling, and the color is slightly changed compared with the part which is not soaked; the impact-resistant coating has no cracks, peeling and obvious deformation; bonding strength: standard state 0.71MPa, 0.53MPa after soaking; the artificial aging resistance coating of 500h has no bulging, cracking and peeling, powdering is 0 grade, and the color change is less than 1 grade.
Note: with reference to low-temperature storage stability, a main coating sample is put into a 1L glass container (130 mm in height, 110mm in diameter and 0.23mm in wall thickness) to a position of 110mm in height, sealed and then put into a low-temperature box at-5 ℃ for 18h, and taken out and then placed for 6h at 23 ℃; after the operation is circulated for 3 times, the container cover is opened, the internal sample is stirred lightly, and the sample is free from agglomeration and composition change; heat storage stability Primary coating test specimens were loaded into the test tubesStandard low temperature storage stability in the same container, to a height of 110 mm. Sealing, placing in a constant temperature box at 50 deg.C, taking out after 1 month, opening container cover, stirring the internal sample lightly, wherein the sample should not have agglomeration, mildew, coagulation and composition change; the wind crack resistance device consists of a fan, a wind tunnel and a test rack, wherein the cross section of the wind tunnel is 16m 2 A square shape; using a fan capable of obtaining wind speed of more than 10m/s to supply air, controlling the wind speed to be 12m/s, and measuring the air flow speed in the wind tunnel by using a hot bulb type or other anemometers; the drying time is carried out according to the specification of a surface dry method B in the GB/T1728-1979 paint film and putty film drying time measuring method standard, and the test is carried out for 1 time at 1h interval; the water resistance is determined according to the rule of the A method in the GB/T1733-1993 standard for the permanent resistance determination of paint films, and the test plate is immersed in tertiary water as defined in the GB/T6682-1992 standard for laboratory water specification and test method. After the test is finished, taking out the test plate, and slightly sucking water attached to the plate surface by using filter paper; after standing in a standard environment for 3 hours, the surface state was observed. Two test plates in the three test plates have no bulging, cracking and stripping, and the color is allowed to slightly change compared with the part which is not soaked; the alkali resistance is determined according to the GB/T9265-1988 rules for determining the alkali resistance of the architectural coating; after the test is finished, taking out the test board, carefully cleaning the board surface with water, slightly sucking the water attached to the board surface with filter paper, placing the test board in a standard environment for 3H, observing the surface state, wherein two test boards in three test boards have no bulging, cracking and peeling, and the color is allowed to slightly change compared with the part which is not soaked; and (3) coating the surface of the test plate with the base coating, the main coating and the surface coating which are sequentially used according to the amount specified in the product specification in the impact resistance manner, and curing in a standard environment for 14d. The test piece is tightly attached to standard sand with the thickness of 20mm, then a spherical weight with the diameter of 50mm and the weight of 530g freely falls from the position with the height of 300mm, and three positions with the distance of 50mm are selected on a test plate; the surface of the test plate is observed by naked eyes, and no crack, peeling and obvious deformation exist; coating the surface of the test panel with the base coating, the main coating and the surface coating which have the temperature change resistance according to the dosage specified in the product specification in sequence, maintaining for 14d in a standard environment, and performing according to the specification of JG/T25-1999 architectural coating freeze-thaw cycle resistance performance measurement method, wherein at least two test panels are required in the three test panelsThe test plate has no chalking, cracking, peeling, bulging and obvious color change; placing the bonding strength test metal frame on a mortar block with the size of 70mm multiplied by 20mm under a standard state, filling the main coating into the frame (the area is 40mm multiplied by 40 mm), leveling the surface by using a scraper, immediately removing the frame to obtain a test plate, and maintaining for 14d in a standard environment; this test was performed in groups of 5 panels. On the tenth day of the maintenance period, the test plate is placed in a horizontal state, epoxy resin 101 adhesive is used for uniformly coating the surface of the test sample, a steel upper clamp is placed on the test plate, and a 1kg weight is added; removing the adhesive overflowing around, standing for 72h, removing weights, maintaining for 14d, measuring the maximum tensile strength, namely the bonding strength after soaking, on a tensile testing machine according to the method of GB/T9779-1988 multilayer building coating, along the vertical direction of the surface of a test piece, measuring the maximum tensile strength at a tensile speed of 5mm/min, manufacturing 5 test plates at the same time, maintaining for 14d, horizontally placing the test piece on standard requirements of a test method for testing the strength of standard sand GB/T17671-1999 cement mortar at the bottom of a water tank, then injecting water to the position 5mm away from the surface of a mortar block, standing for 10d, taking out, placing the side of the test piece downwards, drying for 24h in a constant temperature box at 50 ℃, placing in a standard environment for 24h, and measuring the bonding strength after soaking.
Claims (3)
1. The production method of the anti-wind-crack and impact-resistant real stone paint is characterized by comprising the following steps of:
step one, surface treatment of colored sand: feeding the color sand into a drum mixer, adding a cross-linking agent, discharging after treatment, wherein the cross-linking agent is a mixture of bis- [ gamma- (triethoxysilicon) propyl ] tetrasulfide and bis- [ gamma- (triethoxysilicon) propyl ] -disulfide in a weight ratio of 1: 1, the rotating speed of the drum mixer is 15-20r/min, the rotating speed of a forced stirring paddle is 800-950r/min, and the cross-linking agent accounts for 0.2-0.5% of the color sand; step two, preparation of blended paint slurry: adding neoprene latex into a kneader, adding polyurethane acrylate emulsion, and uniformly mixing, wherein the neoprene latex is cationic neoprene latex with the pH value of 11-12, the solid content of 48-50% and the latex particle size of 50-190 mm, and the solid content of the polyurethane acrylate emulsion is 20-25%; step three, mixing the paint slurry: uniformly mixing the mixed paint slurry, propylene glycol phenyl ether, an accelerator, a defoaming agent, a dispersing agent and a treated color sand drum mixer, wherein the accelerator in the third step is one or more of ethylene thiourea, N' -diethyl thiourea, trimethyl thiourea and acetaldehyde ammonia (1-aminoethanol), the mixed paint slurry is 150 to 250, the propylene glycol phenyl ether is 5 to 15, the accelerator is 3 to 5, the defoaming agent is 1 to 3, the dispersing agent is 7 to 9, and the treated color sand is 1000 to 1100, the color sand in the third step is prepared by uniformly mixing 10 to 20-mesh snow white sand 20 to 40-mesh quartz sand 40, 80-eyepiece quartz sand, 80 to 120-mesh floor yellow according to the weight ratio of 20: 40: 80: 5: 2 through the drum mixer, wherein the rotating speed of the drum mixer is 15 to 20-mesh marble, the rotating speed of a forced stirring paddle is 800 to 9520-mesh, and the weather-crack resistant and impact resistant real paint is obtained.
2. The production method of the wind crack and impact resistant really stone paint as claimed in claim 1, wherein the weight proportion of the neoprene latex in the step is 15 to 20 percent of the polyurethane acrylate emulsion, the rotation speed of a main shaft of the kneader is 20 to 25r/min, the rotation speed of a secondary shaft of the kneader is 10 to 15r/min, the steam pressure is 0.4 to 0.45MPa, and the kneading time is 5 to 10 minutes.
3. The method for producing the wind crack and impact resistant real stone paint as claimed in claim 1, wherein the dispersant in the third step is a mixture of zinc stearate and triethanolamine in a weight ratio of 2: 1, and the defoamer in the third step is one of silicone defoamer TEGO 825 and silicone defoamer TEGO 8030.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110870783.9A CN113683948B (en) | 2021-07-30 | 2021-07-30 | Production method of anti-wind-crack impact-resistant real stone paint |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110870783.9A CN113683948B (en) | 2021-07-30 | 2021-07-30 | Production method of anti-wind-crack impact-resistant real stone paint |
Publications (2)
Publication Number | Publication Date |
---|---|
CN113683948A CN113683948A (en) | 2021-11-23 |
CN113683948B true CN113683948B (en) | 2022-10-11 |
Family
ID=78578337
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202110870783.9A Expired - Fee Related CN113683948B (en) | 2021-07-30 | 2021-07-30 | Production method of anti-wind-crack impact-resistant real stone paint |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN113683948B (en) |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004115565A (en) * | 2002-09-24 | 2004-04-15 | Nippon Tokushu Toryo Co Ltd | Asphalt chipping-resistant material |
JP2006348707A (en) * | 2005-06-20 | 2006-12-28 | Mitsui Kagaku Sanshi Kk | Surface structural body of structure and its construction method |
CN107699123A (en) * | 2017-11-21 | 2018-02-16 | 广西吉宽太阳能设备有限公司 | Stone-like coating and production method |
CN109321124A (en) * | 2018-09-06 | 2019-02-12 | 江苏久诺建材科技股份有限公司 | A kind of flexible real stone paint |
CN110218487A (en) * | 2019-05-22 | 2019-09-10 | 维新制漆(江西)有限公司 | A kind of rail traffic aqueous out-damping coating and its preparation process |
CN111560215A (en) * | 2020-05-13 | 2020-08-21 | 江苏理想空间装饰工程股份有限公司 | Coating material for improving surface strength of stone and application thereof |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH1112532A (en) * | 1997-06-23 | 1999-01-19 | Asahi Chem Ind Co Ltd | Aqueous coating for stone-like finish |
CN109593413A (en) * | 2018-11-07 | 2019-04-09 | 泉州市东宝建材科技有限公司 | A kind of interior wall resistant lacquer and preparation method thereof |
-
2021
- 2021-07-30 CN CN202110870783.9A patent/CN113683948B/en not_active Expired - Fee Related
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004115565A (en) * | 2002-09-24 | 2004-04-15 | Nippon Tokushu Toryo Co Ltd | Asphalt chipping-resistant material |
JP2006348707A (en) * | 2005-06-20 | 2006-12-28 | Mitsui Kagaku Sanshi Kk | Surface structural body of structure and its construction method |
CN107699123A (en) * | 2017-11-21 | 2018-02-16 | 广西吉宽太阳能设备有限公司 | Stone-like coating and production method |
CN109321124A (en) * | 2018-09-06 | 2019-02-12 | 江苏久诺建材科技股份有限公司 | A kind of flexible real stone paint |
CN110218487A (en) * | 2019-05-22 | 2019-09-10 | 维新制漆(江西)有限公司 | A kind of rail traffic aqueous out-damping coating and its preparation process |
CN111560215A (en) * | 2020-05-13 | 2020-08-21 | 江苏理想空间装饰工程股份有限公司 | Coating material for improving surface strength of stone and application thereof |
Also Published As
Publication number | Publication date |
---|---|
CN113683948A (en) | 2021-11-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN110078867B (en) | Core-shell pure acrylic emulsion for exterior wall coating and preparation method and application thereof | |
US11248140B2 (en) | Highly water-resistant, flexible cementitious coating | |
JPH09118573A (en) | Method for forming antiefflorescent coating film on cementalsubstrate | |
CN101230222A (en) | Title-imitating coating and preparation method thereof | |
CN101575475A (en) | Coating material for surface coating of waterproof membrane and preparation method thereof | |
JP5016887B2 (en) | How to paint concrete surface | |
CN107652717A (en) | A kind of exterior wall true stone paint | |
CN108795177B (en) | Waterproof coating and preparation method thereof | |
CN113683948B (en) | Production method of anti-wind-crack impact-resistant real stone paint | |
JP4580170B2 (en) | Mirror surface finishing method of inorganic porous material, and painted product | |
CN106280789A (en) | A kind of double-component silicon third anticracking waterproof coating and preparation method thereof | |
CN109608971B (en) | Water-based exterior wall coating with temperature control and mildew resistance and preparation method thereof | |
CN112574669A (en) | Modified organic silicon coating and preparation method thereof | |
KR102399896B1 (en) | Versatile paint composition with improved thermal insulation and sound insulation properties | |
CN108911593A (en) | A kind of lacquer and preparation method thereof | |
CN113462237A (en) | Multifunctional wall surface repairing agent and preparation method thereof | |
CN112961604A (en) | High-hardness overglaze and preparation method thereof | |
CN106010173A (en) | Building roof waterproof material | |
CN114044654B (en) | Preparation method of inorganic self-repairing anti-permeability material applied to back water surface | |
CN116463045B (en) | Ash rubber waterproof coating and preparation method thereof | |
CN118374181B (en) | Curing agent for wall painting reinforcement and preparation method thereof | |
CN106746915A (en) | A kind of new sand texture coating and preparation method thereof | |
JPS63162770A (en) | Water-base covering composition for cement base plate | |
JP5407625B2 (en) | Painting method | |
CN115725214B (en) | Primer composition |
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 | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20221011 |
|
CF01 | Termination of patent right due to non-payment of annual fee |