CN113603362A - Water-based environment-friendly white glaze with high adhesion and high weather resistance for photovoltaic back plate glass and preparation method thereof - Google Patents
Water-based environment-friendly white glaze with high adhesion and high weather resistance for photovoltaic back plate glass and preparation method thereof Download PDFInfo
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- CN113603362A CN113603362A CN202110712783.6A CN202110712783A CN113603362A CN 113603362 A CN113603362 A CN 113603362A CN 202110712783 A CN202110712783 A CN 202110712783A CN 113603362 A CN113603362 A CN 113603362A
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- water
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- white glaze
- acrylic resin
- soluble acrylic
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 56
- 238000002360 preparation method Methods 0.000 title claims abstract description 26
- 239000005357 flat glass Substances 0.000 title description 17
- 239000011521 glass Substances 0.000 claims abstract description 45
- 238000003756 stirring Methods 0.000 claims description 84
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 78
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 52
- 239000004925 Acrylic resin Substances 0.000 claims description 46
- 229920000178 Acrylic resin Polymers 0.000 claims description 46
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 39
- 239000002904 solvent Substances 0.000 claims description 39
- 238000006243 chemical reaction Methods 0.000 claims description 37
- 239000000178 monomer Substances 0.000 claims description 31
- 239000004408 titanium dioxide Substances 0.000 claims description 26
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 24
- 239000003999 initiator Substances 0.000 claims description 23
- 238000000034 method Methods 0.000 claims description 22
- 239000003795 chemical substances by application Substances 0.000 claims description 21
- 239000000843 powder Substances 0.000 claims description 21
- 238000002156 mixing Methods 0.000 claims description 20
- 239000002994 raw material Substances 0.000 claims description 20
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 13
- 239000002966 varnish Substances 0.000 claims description 13
- 238000002844 melting Methods 0.000 claims description 11
- 239000006185 dispersion Substances 0.000 claims description 10
- 239000002270 dispersing agent Substances 0.000 claims description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 6
- 239000011248 coating agent Substances 0.000 claims description 6
- 238000000576 coating method Methods 0.000 claims description 6
- 230000008018 melting Effects 0.000 claims description 6
- 238000000227 grinding Methods 0.000 claims description 5
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 5
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 5
- 238000005660 chlorination reaction Methods 0.000 claims description 3
- 239000013530 defoamer Substances 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 2
- 229910052793 cadmium Inorganic materials 0.000 claims 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 claims 1
- 239000003002 pH adjusting agent Substances 0.000 claims 1
- 229920001296 polysiloxane Polymers 0.000 claims 1
- 238000004381 surface treatment Methods 0.000 claims 1
- 238000012360 testing method Methods 0.000 abstract description 5
- 230000006750 UV protection Effects 0.000 abstract description 4
- 230000032683 aging Effects 0.000 abstract description 4
- 238000002310 reflectometry Methods 0.000 abstract description 4
- 229910052710 silicon Inorganic materials 0.000 description 35
- 239000010703 silicon Substances 0.000 description 35
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 34
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 24
- 239000003921 oil Substances 0.000 description 15
- 238000001816 cooling Methods 0.000 description 12
- 229910052757 nitrogen Inorganic materials 0.000 description 12
- 230000001105 regulatory effect Effects 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 11
- 239000012986 chain transfer agent Substances 0.000 description 9
- 230000006835 compression Effects 0.000 description 9
- 238000007906 compression Methods 0.000 description 9
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 8
- 239000000498 cooling water Substances 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 8
- 238000006116 polymerization reaction Methods 0.000 description 8
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 7
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 7
- IAXXETNIOYFMLW-COPLHBTASA-N [(1s,3s,4s)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(=C)C)C[C@H]1C2(C)C IAXXETNIOYFMLW-COPLHBTASA-N 0.000 description 7
- 239000002518 antifoaming agent Substances 0.000 description 7
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 229940119545 isobornyl methacrylate Drugs 0.000 description 7
- OZCWUNHGNVXCCO-UHFFFAOYSA-N oxiran-2-ylmethyl hydrogen carbonate Chemical group OC(=O)OCC1CO1 OZCWUNHGNVXCCO-UHFFFAOYSA-N 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- 238000009833 condensation Methods 0.000 description 6
- 230000005494 condensation Effects 0.000 description 6
- 239000011259 mixed solution Substances 0.000 description 6
- 238000004321 preservation Methods 0.000 description 6
- 238000005054 agglomeration Methods 0.000 description 5
- 230000002776 aggregation Effects 0.000 description 5
- 238000003801 milling Methods 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 230000007547 defect Effects 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000006121 base glass Substances 0.000 description 3
- 230000005489 elastic deformation Effects 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 230000035882 stress Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- CUVLMZNMSPJDON-UHFFFAOYSA-N 1-(1-butoxypropan-2-yloxy)propan-2-ol Chemical compound CCCCOCC(C)OCC(C)O CUVLMZNMSPJDON-UHFFFAOYSA-N 0.000 description 2
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 2
- CUDYYMUUJHLCGZ-UHFFFAOYSA-N 2-(2-methoxypropoxy)propan-1-ol Chemical compound COC(C)COC(C)CO CUDYYMUUJHLCGZ-UHFFFAOYSA-N 0.000 description 2
- WAEVWDZKMBQDEJ-UHFFFAOYSA-N 2-[2-(2-methoxypropoxy)propoxy]propan-1-ol Chemical compound COC(C)COC(C)COC(C)CO WAEVWDZKMBQDEJ-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- RNFAKTRFMQEEQE-UHFFFAOYSA-N Tripropylene glycol butyl ether Chemical compound CCCCOC(CC)OC(C)COC(O)CC RNFAKTRFMQEEQE-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 238000005265 energy consumption Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000002186 photoactivation Effects 0.000 description 2
- -1 polydimethylsiloxane Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 1
- JJRDRFZYKKFYMO-UHFFFAOYSA-N 2-methyl-2-(2-methylbutan-2-ylperoxy)butane Chemical compound CCC(C)(C)OOC(C)(C)CC JJRDRFZYKKFYMO-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- VTCVEAWGRGJXPA-UHFFFAOYSA-N CCCC=CCC(C=C)(C=C1)C(C2=CC=CC=C2)=CC1(C)C1=CC=CC=C1 Chemical compound CCCC=CCC(C=C)(C=C1)C(C2=CC=CC=C2)=CC1(C)C1=CC=CC=C1 VTCVEAWGRGJXPA-UHFFFAOYSA-N 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical group CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- 229920002396 Polyurea Polymers 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical group CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 239000012972 dimethylethanolamine Substances 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical group CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 239000012767 functional filler Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000004224 protection Effects 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C8/00—Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C1/00—Ingredients generally applicable to manufacture of glasses, glazes, or vitreous enamels
- C03C1/02—Pretreated ingredients
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/006—Surface treatment of glass, not in the form of fibres or filaments, by coating with materials of composite character
-
- 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
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C2217/00—Coatings on glass
- C03C2217/20—Materials for coating a single layer on glass
- C03C2217/29—Mixtures
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C2217/00—Coatings on glass
- C03C2217/70—Properties of coatings
- C03C2217/78—Coatings specially designed to be durable, e.g. scratch-resistant
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Geochemistry & Mineralogy (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Composite Materials (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Paints Or Removers (AREA)
Abstract
本发明公开了一种高附着力高耐候性光伏背板玻璃用水性环保白色釉料，由调墨油、分散剂、低熔点玻璃粉、钛白粉、流平剂以及消泡剂组成，可用于制备光伏背板玻璃的高附着力、高耐候性釉层，将其应用于光伏组件上，反射率大于78％，附着力达0级，且耐候性试验(耐紫外性能、PCT耐老化性能)反射率衰减率均值均小于1％。The invention discloses a water-based environment-friendly white glaze for photovoltaic backplane glass with high adhesion and high weather resistance. Preparation of high-adhesion, high-weather-resistant glaze layer of photovoltaic backplane glass, applied to photovoltaic modules, the reflectivity is greater than 78%, the adhesion is up to grade 0, and the weather resistance test (ultraviolet resistance, PCT aging resistance) The mean value of reflectance decay rate is less than 1%.
Description
Technical Field
The invention relates to the technical field of photovoltaic modules and glass glazes, in particular to a water-based environment-friendly white glaze with high adhesion and high weather resistance for photovoltaic back plate glass, a preparation method of the water-based environment-friendly white glaze and application of the water-based environment-friendly white glaze in photovoltaic module glass.
Background
The double-glass photovoltaic module consists of front plate glass, back plate glass, solar cells and the like, wherein the cells are connected in series and in parallel by leads and collected to a lead terminal to form the photovoltaic cell module, and the double-glass photovoltaic module is particularly suitable for relatively harsh climatic environments, such as photovoltaic power stations in areas with high humidity. For effectively promoting dual glass assembly's efficiency, except using white encapsulating material such as EVA and POE, still can pass through on the silk screen printing technology coating photovoltaic backplate glass white frit, can reflect the light that sees through the battery piece clearance to the battery piece surface through the glaze layer and be recycled, and then promote photovoltaic assembly's conversion efficiency.
However, the existing white glaze has some problems to be solved, such as adhesion force can not reach grade 1 (generally grade 2); the reflectivity attenuation rate in weather resistance tests (ultraviolet resistance and PCT aging resistance) is large, and the like, so that the glass is not well applicable to photovoltaic glass.
Disclosure of Invention
In order to overcome the defects of the prior art, the invention aims to provide the water-based environment-friendly white glaze with high adhesion and high weather resistance for the photovoltaic back plate glass, and the water-based environment-friendly white glaze has excellent adhesion and weather resistance when being applied to the photovoltaic glass.
The invention adopts the following technical scheme:
the water-based environment-friendly white glaze with high adhesive force and high weather resistance for the photovoltaic back plate glass comprises the following raw material components in parts by weight:
the ink mixing oil comprises organic silicon modified water-soluble acrylic resin, and the organic silicon modified water-soluble acrylic resin is prepared by a homogeneous one-step method; the low-melting-point glass powder is a lead-free and cadmium-free low-melting-point Bi-Zn-B system.
The organic silicon monomer in the raw material components of the organic silicon modified water-soluble acrylic resin used for the ink mixing oil has good wettability to low-melting-point glass powder and titanium dioxide coated by silicon oxide and aluminum oxide, so that the compatibility of the whole system is increased, and the dispersion and grinding efficiency of the prepared white glaze is improved.
According to some preferred embodiments of the invention, the varnish comprises the following raw material components in parts by weight: 60-80 parts of an alcohol ether solvent, 20-40 parts of organic silicon modified water-soluble acrylic resin and 1-5 parts of a rheological anti-settling agent; the raw material components of the organic silicon modified water-soluble acrylic resin comprise 5-10 parts of organic silicon monomer.
According to some preferred embodiment aspects of the invention, the alcohol ether solvent in the varnish is selected from one or more of diethylene glycol butyl ether, dipropylene glycol methyl ether, tripropylene glycol methyl ether, dipropylene glycol butyl ether and tripropylene glycol butyl ether.
According to some preferred embodiments of the present invention, the silicone-modified water-soluble acrylic resin has a viscosity of 10000 ± 2000mpa · s (25 ± 1 ℃); the solid content of the organic silicon modified water-soluble acrylic resin is 50-60%. The organic silicon modified water-soluble acrylic resin with the viscosity range is prepared into water-based varnish with moderate viscosity on the basis of ensuring the number of effective adhesives, and the integral viscosity of a glaze system is ensured after functional fillers such as glass powder, titanium dioxide and the like in a quantitative range are added.
According to some preferred embodiments of the invention, the rheological anti-settling agent is selected from one or more of fumed silica, organobentonite, and modified polyurea solution.
According to some preferred embodiments of the present invention, the silicone-modified water-soluble acrylic resin comprises the following raw material components in parts by weight:
according to some preferred embodiments of the present invention, the silicone-modified water-soluble acrylic resin is prepared by:
mixing an acrylic monomer and/or an acrylate monomer, styrene, an organic silicon monomer, a molecular weight regulator and a part of initiator, uniformly mixing, dropwise adding into a part of alcohol ether solvent with the temperature of 140-150 ℃, controlling the dropwise adding time to be 6-8h, and carrying out heat preservation reaction for 1-2h after the dropwise adding is finished; adding the rest of initiator into the system, and continuing to react for 1-2 h; cooling to 70-80 deg.C, adding the rest alcohol ether solvent, and mixing; and adjusting the pH value of the system to 8-9 by using an organic amine neutralizer to obtain the organic silicon modified water-soluble acrylic resin.
According to some preferred embodiments of the present invention, the part of the alcohol ether solvent accounts for 40-60% of the total mass of the alcohol ether solvent in the raw material of the organosilicon modified water-soluble acrylic resin; the partial initiator accounts for 80-95% of the total mass of the initiators in the raw materials of the organosilicon modified water-soluble acrylic resin. The alcohol ether solvent is added in two times, and the purpose is to reduce the heating time in the synthetic process of the organic silicon modified water-soluble acrylic resin, and simultaneously reduce the cooling time and the usage amount of cooling water, thereby reducing the energy consumption in the production process. The initiator is added twice, and the purpose is that the initiator supplemented twice is initiated at the temperature of 140-150 ℃, so that the residual monomer is polymerized again, and further the conversion rate of the organosilicon modified water-soluble acrylic resin is improved.
The preparation method has the following two advantages:
(1) acrylic acid monomer and/or acrylate monomer, styrene, organic silicon monomer, molecular weight regulator, partial initiator and the like are uniformly mixed and dripped into a reaction kettle under the condition of homogeneous phase, molecular chains are increased through the fracture and polymerization of double bonds of acrylic acid (ester), styrene, vinyl and the like in the whole process, and the polymerization molecular weight is controlled through the molecular weight regulator (chain transfer agent), so that the viscosity of the organic silicon modified water-soluble acrylic resin obtained by the homogeneous one-step method is relatively low. Compared with the mode of synthesizing silica sol in advance or polymerizing acrylic resin in advance, the method has the advantages that the process is simplified, the organic silicon monomer and other raw materials are uniformly mixed in advance, then the mixture is dripped into an alcohol ether solvent to react, double bonds are cracked and polymerized synchronously with the acrylic monomer and/or acrylate monomer and styrene, and the uniformity of the organic silicon monomer is better. And the organosilicon can reduce the surface energy, has better wettability to glass powder and titanium dioxide, and then increases the compatibility of the whole system, and promotes the dispersion and grinding efficiency of the prepared white glaze.
(2) The temperature of the system is reduced to 70-80 ℃, and the residual alcohol ether solvent is added to continue to be stirred and mixed evenly. By adopting the method, the heating time in the synthetic process of the organic silicon modified water-based acrylic resin can be reduced, and the cooling time and the use amount of cooling water are reduced, so that the energy consumption in the production process is reduced.
In some embodiments of the present invention, the polymerization preparation of the silicone-modified water-soluble acrylic resin specifically comprises the following steps:
(a) keeping the reaction kettle clean and anhydrous, adding 20-40 parts by weight of alcohol ether solvent, introducing nitrogen into the reaction kettle and keeping the nitrogen, introducing cooling water into a condensation pipe, and heating the alcohol ether solvent to 140-150 ℃.
(b) Taking another dispersion kettle, and sequentially adding 10-15 parts of tertiary carbonic acid glycidyl ester, 5-10 parts of hydroxyethyl acrylate, 1-5 parts of methyl methacrylate, 3-6 parts of acrylic acid, 5-10 parts of isobornyl methacrylate, 25-35 parts of butyl acrylate, 10-20 parts of styrene, 5-10 parts of organosilicon monomer, 1-2 parts of molecular weight regulator (chain transfer agent) and 2-5 parts of initiator according to parts by weight; stirring and mixing uniformly, wherein the stirring speed is 200-; dropwise adding the mixed solution (a homogeneous system formed by the mixed monomer, the molecular weight regulator (chain transfer agent) and the initiator) into the reaction kettle in the step (a), wherein the dropwise adding time is 6-8h, and the temperature is controlled at 140-; after the dropwise addition, the reaction is carried out for 1-2h under the condition that the temperature is controlled at 140 ℃ and 150 ℃.
(c) Adding 0.1-0.3 part of initiator into the reaction kettle in the step (a) by weight part, and continuing to react for 1-2h, wherein the temperature is controlled at 140-.
(d) Cooling to 70-80 ℃, adding 20-40 parts of alcohol ether solvent, stirring and mixing uniformly, wherein the stirring speed is 400-500r/min, and the stirring time is 20-30 min.
(e) Stirring and dripping 10-15% of pH regulator, adjusting the pH value to 8.0-9.0, stirring at the rotation speed of 400-500r/min, and stirring for 20-30 min.
According to some preferred embodiment aspects of the present invention, the alcohol ether solvent in the silicone-modified water-soluble acrylic resin is selected from one or more of diethylene glycol butyl ether, dipropylene glycol methyl ether, tripropylene glycol methyl ether, dipropylene glycol butyl ether, and tripropylene glycol butyl ether.
According to some preferred embodiments of the invention, the acrylic monomer is acrylic acid; the acrylate monomer is one or more of tertiary carbonic acid glycidyl ester, hydroxyethyl acrylate, methyl methacrylate, isobornyl methacrylate and butyl acrylate. The organic silicon monomer is vinyl triethoxysilane and/or 3- (methacryloyloxy) propyl trimethoxysilane. The organosilicon monomer and other raw materials are mixed uniformly in advance, and then the mixture is dripped into an alcohol ether solvent to react, and the double bonds are cracked and polymerized synchronously with an acrylic monomer and/or an acrylate monomer and styrene, so that the organosilicon monomer has better uniformity. And the organosilicon can reduce the surface energy, has better wettability to glass powder and titanium dioxide, further increases the compatibility of the whole system, and improves the dispersion and grinding efficiency of the prepared water-based environment-friendly white glaze.
According to some preferred embodiments of the invention, the molecular weight regulator (chain transfer agent) is a 2, 4-diphenyl-4-methyl-1-pentenylmethylstyrene linear dimer. The initiator is di-tert-butyl peroxide and/or di-tert-amyl peroxide. The pH regulator is an organic amine neutralizer, and the organic amine neutralizer is dimethylethanolamine and/or 2-amino-2-methyl-1-propanol.
According to some preferred embodiments of the invention, the dispersant is an aqueous high molecular polymer, such as TEGO 755W.
According to some preferred embodiments of the invention, the softening temperature of the low-melting-point glass powder is 400-500 ℃, preferably 450 ℃, and the total melting temperature is 500-550 ℃, preferably 520 ℃, so that the aqueous environment-friendly white glaze is completely melted in a short time within the tempering temperature range of 600-720 ℃, thereby ensuring the high adhesion of the glaze layer. The linear expansion coefficient of the sheet glass is generally 85 x 10-7The linear expansion coefficient of the low-melting-point glass powder is 75-80 to 10-7The temperature is 30-300 ℃, the coefficient of linear expansion of the glaze layer is lower than that of the base glass, the shrinkage of the glaze layer is smaller than that of the base in the cooling process, the glaze layer is automatically deformed under the self-shrinkage effect and also under the compression effect given by the shrinkage of the base, and the permanent compression stress is generated due to the compression elastic deformation, so that the adhesion of the glaze layer is improved.
According to some preferred embodiments of the invention, the titanium dioxide is prepared by a chlorination method, the titanium dioxide prepared by the method has extremely low impurity content, and the silicon oxide and the aluminum oxide are used for coating, so that lattice defects caused by the titanium dioxide under the ultraviolet irradiation condition can be blocked, light activation points on the surface of the titanium dioxide are shielded, and the weather resistance and the chemical stability of the titanium dioxide are improved.
According to some preferred embodiments of the present invention, the raw material composition of the aqueous environmentally-friendly white glaze further comprises 0.5-1.0 part of a leveling agent and 0.5-1.0 part of a defoaming agent. In some embodiments, the leveling agent is a polyether siloxane copolymer; preferably, the defoamer is a polyether modified polydimethylsiloxane interpolymer.
The invention also provides a preparation method of the water-based environment-friendly white glaze with high adhesion and weather resistance for the photovoltaic back plate glass, which comprises the following steps:
(1) preparing ink mixing oil: under the stirring condition, the alcohol ether solvent, the organic silicon modified water-soluble acrylic resin and the rheological anti-settling agent are sequentially put into a stirring kettle according to the weight parts, and are stirred uniformly to obtain the ink-regulating oil. The stirring speed is 400-600r/min, and the stirring time is 40-60 min.
(2) Preparing water-based environment-friendly white glaze: putting the ink adjusting oil into a container according to the parts by weight, starting stirring at the rotating speed of 400-; putting the dispersing agent into a container, and stirring uniformly for 20-30 min; regulating the rotating speed to 800-; regulating the rotating speed to 400-600r/min, sequentially putting the flatting agent and the defoaming agent into a container, and stirring the mixture until the mixture is uniform, wherein the stirring time is 20-30 min. And grinding by a three-roll mill (three-roll mill) to obtain the water-based environment-friendly white glaze with the fineness of less than 10 mu m.
Due to the adoption of the technical scheme, compared with the prior art, the invention has the following advantages: the water-based environment-friendly white glaze with high adhesion and weather resistance for the photovoltaic back plate glass is prepared by selecting the low-melting-point glass powder with the softening temperature of 400-550 ℃ and the full-melting temperature of 500-550 ℃, so that the water-based environment-friendly white glaze is completely melted in a short time within the toughening temperature range of 600-720 ℃, and the high adhesion of the glaze layer is further ensured. The coefficient of expansion of the sheet glass is generally 85 x 10-7The linear expansion coefficient of the low-melting-point glass powder is 75 to 80 to 10 per kilogram (K is 30 to 300 ℃), and-7the temperature is 30-300 ℃, the coefficient of linear expansion of the glaze layer is lower than that of the base glass, the shrinkage of the glaze layer is smaller than that of the base in the cooling process, the glaze layer is automatically deformed under the self-shrinkage effect and also under the compression effect given by the shrinkage of the base, and the permanent compression stress is generated due to the compression elastic deformation, so that the adhesion of the glaze layer is improved. The titanium dioxide prepared by the method has extremely low impurity content, and the coating treatment by using silicon oxide and aluminum oxide can block the lattice defect of the titanium dioxide caused under the ultraviolet irradiation condition, shield the photoactivation point on the surface of the titanium dioxide, and improve the weather resistance and the chemical stability of the titanium dioxideAnd (5) performing qualitative determination.
Detailed Description
In order to make those skilled in the art better understand the technical solution of the present invention, the following will clearly and completely describe the technical solution in conjunction with the embodiments of the present invention, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
Example 1
The preparation of the water-based environment-friendly white glaze for the photovoltaic back plate glass with high adhesion and high weather resistance in the embodiment comprises the following steps:
(1) polymerization preparation of organosilicon modified water-soluble acrylic resin:
(a) keeping the reaction kettle clean and anhydrous, adding 40 parts by weight of alcohol ether solvent, introducing nitrogen into the reaction kettle and keeping the nitrogen, introducing cooling water into a condensation pipe, and heating the alcohol ether solvent to 140 ℃.
(b) Taking another dispersion kettle, and sequentially adding 10 parts of tertiary carbonic acid glycidyl ester, 5 parts of hydroxyethyl acrylate, 3 parts of methyl methacrylate, 5 parts of acrylic acid, 10 parts of isobornyl methacrylate, 25 parts of butyl acrylate, 15 parts of styrene, 5 parts of organic silicon monomer, 2 parts of molecular weight regulator (chain transfer agent) and 3.5 parts of initiator according to parts by weight; stirring and mixing uniformly, wherein the stirring speed is 300r/min, and the stirring time is 40 min; dropwise adding the mixed solution into the reaction kettle in the step (a), wherein the dropwise adding time is 6 hours, and the temperature is controlled at 140 ℃; after the dropwise addition, the reaction is carried out for 2 hours under the condition of heat preservation, and the temperature is controlled at 140 ℃.
(c) Adding 0.2 part of initiator by weight into the reaction kettle in the step (a), and continuing to react for 2 hours, wherein the temperature is controlled at 140 ℃.
(d) Cooling to 80 ℃, adding 40 parts by weight of alcohol ether solvent, and uniformly stirring and mixing at the stirring speed of 400r/min for 30 min.
(e) And (3) dropwise adding a pH regulator with the mass concentration of 10%, adjusting the pH value to 8.0, stirring at the rotating speed of 400r/min for 20min, and thus obtaining the organic silicon modified water-soluble acrylic resin.
(2) Preparing water-based varnish:
under the stirring condition, 60 parts of alcohol ether solvent, 32.5 parts of organic silicon modified water-soluble acrylic resin and 5 parts of rheological anti-settling agent are sequentially put into a stirring kettle in parts by weight, and are stirred uniformly at the stirring speed of 400r/min for 60min to obtain the water-based ink-regulating oil.
(3) Preparation of water-based environment-friendly white glaze
The water-based environment-friendly white glaze comprises the following raw material components in parts by weight:
putting the ink adjusting oil into a container according to the parts by weight, and stirring at the rotating speed of 400 r/min; putting the dispersing agent into a container, and stirring uniformly for 20 min; regulating the rotating speed to 1000r/min, sequentially putting the low-melting-point glass powder and the titanium dioxide into a container according to the parts by weight, and stirring until the mixture is uniform and free of agglomeration for 900 min; regulating the rotating speed to 400r/min, sequentially putting the flatting agent and the defoaming agent into a container, and stirring uniformly for 30 min. And then the water-based environment-friendly white glaze is obtained by three-roller milling to obtain the fineness of less than 10 mu m.
Example 2
The preparation of the water-based environment-friendly white glaze for the photovoltaic back plate glass with high adhesion and high weather resistance in the embodiment comprises the following steps:
(1) polymerization preparation of organosilicon modified water-soluble acrylic resin:
(a) keeping the reaction kettle clean and anhydrous, adding 40 parts by weight of alcohol ether solvent, introducing nitrogen into the reaction kettle and keeping the nitrogen, introducing cooling water into a condensation pipe, and heating the alcohol ether solvent to 150 ℃.
(b) Taking another dispersion kettle, and sequentially adding 15 parts of tertiary carbonic acid glycidyl ester, 5 parts of hydroxyethyl acrylate, 5 parts of methyl methacrylate, 5 parts of acrylic acid, 5 parts of isobornyl methacrylate, 35 parts of butyl acrylate, 15 parts of styrene, 5 parts of organic silicon monomer, 1.5 parts of molecular weight regulator (chain transfer agent) and 4 parts of initiator according to parts by weight; stirring and mixing uniformly, wherein the stirring speed is 300r/min, and the stirring time is 30 min; dropwise adding the mixed solution into the reaction kettle in the step (a), wherein the dropwise adding time is 6 hours, and the temperature is controlled at 150 ℃; after the dropwise addition, the reaction is carried out for 2 hours under the condition of heat preservation, and the temperature is controlled at 150 ℃.
(c) Adding 0.3 part of initiator by weight into the reaction kettle in the step (a), and continuing to react for 2 hours, wherein the temperature is controlled at 150 ℃.
(d) Cooling to 70 ℃, adding 40 parts by weight of alcohol ether solvent, and uniformly stirring and mixing at the stirring speed of 400r/min for 30 min.
(e) And (3) dropwise adding a pH regulator with the mass concentration of 15%, adjusting the pH value to 9.0, stirring at the rotating speed of 400r/min for 30min, and thus obtaining the organic silicon modified water-soluble acrylic resin.
(2) Preparing water-based varnish:
under the stirring condition, according to the weight portion, 70 portions of alcohol ether solvent, 25 portions of organic silicon modified water-soluble acrylic resin and 3 portions of rheological anti-settling agent are sequentially put into a stirring kettle and stirred uniformly, the stirring speed is 400r/min, and the stirring time is 50min, so that the water-based ink-adjusting oil is obtained.
(3) Preparation of water-based environment-friendly white glaze
The white glaze comprises the following raw materials in parts by weight:
putting the ink adjusting oil into a container according to the parts by weight, and stirring at the rotating speed of 600 r/min; putting the dispersing agent into a container, and stirring uniformly for 20 min; regulating the rotating speed to 800r/min, sequentially putting the low-melting-point glass powder and the titanium dioxide into a container according to the parts by weight, and stirring until the mixture is uniform and free of agglomeration for 120 min; regulating the rotating speed to 400r/min, sequentially putting the flatting agent and the defoaming agent into a container, and stirring uniformly for 20 min. And then the water-based environment-friendly white glaze is obtained by three-roller milling to obtain the fineness of less than 10 mu m.
Example 3
The preparation of the water-based environment-friendly white glaze for the photovoltaic back plate glass with high adhesion and high weather resistance in the embodiment comprises the following steps:
(1) polymerization preparation of organosilicon modified water-soluble acrylic resin:
(a) keeping the reaction kettle clean and anhydrous, adding 40 parts by weight of alcohol ether solvent, introducing nitrogen into the reaction kettle and keeping the nitrogen, introducing cooling water into a condensation pipe, and heating the alcohol ether solvent to 145 ℃.
(b) Taking another dispersion kettle, and sequentially adding 12 parts of tertiary carbonic acid glycidyl ester, 10 parts of hydroxyethyl acrylate, 5 parts of methyl methacrylate, 3 parts of acrylic acid, 10 parts of isobornyl methacrylate, 30 parts of butyl acrylate, 10 parts of styrene, 8 parts of organic silicon monomer, 2 parts of molecular weight regulator (chain transfer agent) and 5 parts of initiator according to parts by weight; stirring and mixing uniformly, wherein the stirring speed is 300r/min, and the stirring time is 30 min; dropwise adding the mixed solution into the reaction kettle in the step (a), wherein the dropwise adding time is 8h, and the temperature is controlled at 145 ℃; after the dropwise addition, the reaction is carried out for 2 hours under the condition of heat preservation, and the temperature is controlled to be 145 ℃.
(c) Adding 0.3 part of initiator by weight into the reaction kettle in the step (a), and continuing the reaction for 1 hour, wherein the temperature is controlled at 145 ℃.
(d) Cooling to 75 ℃, adding 30 parts by weight of alcohol ether solvent, and uniformly stirring and mixing, wherein the stirring speed is 400r/min, and the stirring time is 30 min.
(e) Dropwise adding a pH regulator with the mass concentration of 15%, adjusting the pH value to 8.5, stirring at the rotating speed of 400r/min for 30min, and thus obtaining the organic silicon modified water-soluble acrylic resin.
(2) Preparing water-based varnish:
under the stirring condition, 65 parts of alcohol ether solvent, 25 parts of organic silicon modified water-soluble acrylic resin and 5 parts of rheological anti-settling agent are sequentially put into a stirring kettle in parts by weight, and are stirred uniformly at the stirring speed of 400r/min for 50min to obtain the water-based ink-regulating oil.
(3) Preparation of water-based environment-friendly white glaze
The white glaze comprises the following raw materials in parts by weight:
putting the ink adjusting oil into a container according to the parts by weight, and stirring at the rotating speed of 400 r/min; putting the dispersing agent into a container according to the weight parts, and stirring the dispersing agent uniformly for 25 min; regulating the rotating speed to 1000r/min, sequentially putting the low-melting-point glass powder and the titanium dioxide into a container, and stirring until the mixture is uniform and free of agglomeration for 100 min; regulating the rotating speed to 400r/min, sequentially putting the flatting agent and the defoaming agent into a container, and stirring uniformly for 20 min. And then the water-based environment-friendly white glaze is obtained by three-roller milling to obtain the fineness of less than 10 mu m.
Comparative example 1
The preparation of the white glaze in this comparative example differs from the previous examples mainly in that the titanium dioxide in this comparative example was prepared by the sulfuric acid method and was not coated with silica and alumina. The preparation of the white glaze in this comparative example comprises the following steps:
(1) polymerization preparation of organosilicon modified water-soluble acrylic resin:
(a) keeping the reaction kettle clean and anhydrous, adding 40 parts by weight of alcohol ether solvent, introducing nitrogen into the reaction kettle and keeping the nitrogen, introducing cooling water into a condensation pipe, and heating the alcohol ether solvent to 140 ℃.
(b) Taking another dispersion kettle, and sequentially adding 10 parts of tertiary carbonic acid glycidyl ester, 5 parts of hydroxyethyl acrylate, 3 parts of methyl methacrylate, 5 parts of acrylic acid, 10 parts of isobornyl methacrylate, 25 parts of butyl acrylate, 15 parts of styrene, 5 parts of organic silicon monomer, 2 parts of molecular weight regulator (chain transfer agent) and 3.5 parts of initiator according to parts by weight; stirring and mixing uniformly, wherein the stirring speed is 300r/min, and the stirring time is 40 min; dropwise adding the mixed solution into the reaction kettle in the step (a), wherein the dropwise adding time is 6 hours, and the temperature is controlled at 140 ℃; after the dropwise addition, the reaction is carried out for 2 hours under the condition of heat preservation, and the temperature is controlled at 140 ℃.
(c) Adding 0.2 part of initiator by weight into the reaction kettle in the step (a), and continuing to react for 2 hours, wherein the temperature is controlled at 140 ℃.
(d) Cooling to 80 ℃, adding 40 parts by weight of alcohol ether solvent, and uniformly stirring and mixing at the stirring speed of 400r/min for 30 min.
(e) And (3) dropwise adding a pH regulator with the mass concentration of 10%, adjusting the pH value to 8.0, stirring at the rotating speed of 400r/min for 20min, and thus obtaining the organic silicon modified water-soluble acrylic resin.
(2) Preparing water-based varnish:
under the stirring condition, 60 parts of alcohol ether solvent, 32.5 parts of organic silicon modified water-soluble acrylic resin and 5 parts of rheological anti-settling agent are sequentially put into a stirring kettle in parts by weight, and are stirred uniformly at the stirring speed of 400r/min for 60min to obtain the water-based ink-regulating oil.
(3) Preparation of water-based environment-friendly white glaze
The water-based environment-friendly white glaze comprises the following raw material components in parts by weight:
putting the ink adjusting oil into a container according to the parts by weight, and stirring at the rotating speed of 400 r/min; putting the dispersing agent into a container, and stirring uniformly for 20 min; regulating the rotating speed to 1000r/min, sequentially putting the low-melting-point glass powder and titanium dioxide in a container according to the parts by weight, wherein the titanium dioxide is prepared by a sulfuric acid method, is not subjected to coating treatment of silicon peroxide and alumina, and is stirred until the mixture is uniform and free of agglomeration, and the stirring time is 900 min; regulating the rotating speed to 400r/min, sequentially putting the flatting agent and the defoaming agent into a container, and stirring uniformly for 30 min. And then the water-based environment-friendly white glaze is obtained by three-roller milling to obtain the fineness of less than 10 mu m.
Comparative example 2
The main difference between the preparation of the white glaze in this comparative example and the previous examples is that the low melting point glass powder selected in this comparative example has a softening temperature of 480 ℃, a total melting temperature of 550 ℃, and a linear expansion coefficient of 110-115-10 at 30-300--7and/K. The preparation of the white glaze in this comparative example comprises the following steps:
(1) polymerization preparation of organosilicon modified water-soluble acrylic resin:
(a) keeping the reaction kettle clean and anhydrous, adding 40 parts by weight of alcohol ether solvent, introducing nitrogen into the reaction kettle and keeping the nitrogen, introducing cooling water into a condensation pipe, and heating the alcohol ether solvent to 140 ℃.
(b) Taking another dispersion kettle, and sequentially adding 10 parts of tertiary carbonic acid glycidyl ester, 5 parts of hydroxyethyl acrylate, 3 parts of methyl methacrylate, 5 parts of acrylic acid, 10 parts of isobornyl methacrylate, 25 parts of butyl acrylate, 15 parts of styrene, 5 parts of organic silicon monomer, 2 parts of molecular weight regulator (chain transfer agent) and 3.5 parts of initiator according to parts by weight; stirring and mixing uniformly, wherein the stirring speed is 300r/min, and the stirring time is 40 min; dropwise adding the mixed solution into the reaction kettle in the step (a), wherein the dropwise adding time is 6 hours, and the temperature is controlled at 140 ℃; after the dropwise addition, the reaction is carried out for 2 hours under the condition of heat preservation, and the temperature is controlled at 140 ℃.
(c) Adding 0.2 part of initiator by weight into the reaction kettle in the step (a), and continuing to react for 2 hours, wherein the temperature is controlled at 140 ℃.
(d) Cooling to 80 ℃, adding 40 parts by weight of alcohol ether solvent, and uniformly stirring and mixing at the stirring speed of 400r/min for 30 min.
(e) And (3) dropwise adding a pH regulator with the mass concentration of 10%, adjusting the pH value to 8.0, stirring at the rotating speed of 400r/min for 20min, and thus obtaining the organic silicon modified water-soluble acrylic resin.
(2) Preparing water-based varnish:
under the stirring condition, 60 parts of alcohol ether solvent, 32.5 parts of organic silicon modified water-soluble acrylic resin and 5 parts of rheological anti-settling agent are sequentially put into a stirring kettle in parts by weight, and are stirred uniformly at the stirring speed of 400r/min for 60min to obtain the water-based ink-regulating oil.
(3) Preparation of water-based environment-friendly white glaze
The water-based environment-friendly white glaze comprises the following raw material components in parts by weight:
putting the ink adjusting oil into a container according to the parts by weight, and stirring at the rotating speed of 400 r/min; putting the dispersing agent into a container, and stirring uniformly for 20 min; regulating the rotating speed to 1000r/min, sequentially putting the low-melting-point glass powder and the titanium dioxide into a container according to the parts by weight, wherein the softening temperature of the low-melting-point glass powder is 480 ℃, the total melting temperature is 550 ℃, and the linear expansion coefficient at 30-300 ℃ is 110--7and/K. Stirring for 900min until the mixture is uniform and has no agglomeration; regulating the rotating speed to 400r/min, sequentially putting the flatting agent and the defoaming agent into a container, and stirring uniformly for 30 min. And then the water-based environment-friendly white glaze is obtained by three-roller milling to obtain the fineness of less than 10 mu m.
Example 4
The aqueous environmentally friendly white glaze materials in examples 1 to 3 and comparative example 1 were coated on photovoltaic module glass and cured for testing, and the results are shown in table 1.
TABLE 1 test results
The results in Table 1 show that the UV resistance and the PCT aging resistance of examples 1 to 3 are superior to those of comparative example 1, and the short side part of the glass of comparative example 2 has cracks and the adhesion is grade 1. In the embodiment, the softening temperature of the low-melting-point glass powder is 400-550 ℃, and the total melting temperature is 500-550 ℃, so that the aqueous environment-friendly effect is achievedThe white glaze material is completely melted in a short time within the toughening temperature range of 600-720 ℃, thereby ensuring the high adhesive force of the glaze layer. The coefficient of expansion of the sheet glass is generally 85 x 10-7The linear expansion coefficient of the low-melting-point glass powder is 75 to 80 to 10 per kilogram (K is 30 to 300 ℃), and-7the temperature is 30-300 ℃, the coefficient of linear expansion of the glaze layer is lower than that of the base glass, the shrinkage of the glaze layer is smaller than that of the base in the cooling process, the glaze layer is automatically deformed under the self-shrinkage effect and also under the compression effect given by the shrinkage of the base, and the permanent compression stress is generated due to the compression elastic deformation, so that the adhesion of the glaze layer is improved. The titanium dioxide is prepared by a chlorination method, the content of impurities in the titanium dioxide prepared by the method is extremely low, and the silicon oxide and the aluminum oxide are used for coating, so that the lattice defect of the titanium dioxide caused under the ultraviolet irradiation condition can be blocked, the photoactivation point on the surface of the titanium dioxide is shielded, and the weather resistance and the chemical stability of the titanium dioxide are improved.
The water-based environment-friendly white glaze with high adhesion and high weather resistance for the photovoltaic back plate glass can be used for a glaze layer with high adhesion and high weather resistance for the photovoltaic back plate glass, the reflectivity is more than 78%, the adhesion reaches 0 level, and the mean values of the reflectivity attenuation rates of weather resistance tests (ultraviolet resistance and PCT aging resistance) are less than 1%.
The above embodiments are merely illustrative of the technical concept and features of the present invention, and the purpose thereof is to enable those skilled in the art to understand the content of the present invention and implement the invention, and not to limit the scope of the invention, and all equivalent changes or modifications made according to the spirit of the present invention should be covered by the scope of the present invention.
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