CN112142338A - Glass reinforcing liquid, composite chemically strengthened glass and preparation method thereof - Google Patents
Glass reinforcing liquid, composite chemically strengthened glass and preparation method thereof Download PDFInfo
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- CN112142338A CN112142338A CN201910574776.7A CN201910574776A CN112142338A CN 112142338 A CN112142338 A CN 112142338A CN 201910574776 A CN201910574776 A CN 201910574776A CN 112142338 A CN112142338 A CN 112142338A
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- glass
- reinforcing liquid
- chemically strengthened
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- 239000011521 glass Substances 0.000 title claims abstract description 140
- 230000003014 reinforcing effect Effects 0.000 title claims abstract description 85
- 239000007788 liquid Substances 0.000 title claims abstract description 79
- 239000005345 chemically strengthened glass Substances 0.000 title claims abstract description 60
- 239000002131 composite material Substances 0.000 title claims abstract description 45
- 238000002360 preparation method Methods 0.000 title abstract description 24
- 239000011347 resin Substances 0.000 claims abstract description 37
- 229920005989 resin Polymers 0.000 claims abstract description 37
- 239000002904 solvent Substances 0.000 claims abstract description 31
- 229920002678 cellulose Polymers 0.000 claims abstract description 26
- 239000001913 cellulose Substances 0.000 claims abstract description 26
- 239000012752 auxiliary agent Substances 0.000 claims abstract description 25
- 239000002994 raw material Substances 0.000 claims abstract description 12
- 238000004383 yellowing Methods 0.000 claims abstract description 8
- 239000000853 adhesive Substances 0.000 claims abstract description 7
- 230000001070 adhesive effect Effects 0.000 claims abstract description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 5
- 239000000758 substrate Substances 0.000 claims description 42
- 238000005507 spraying Methods 0.000 claims description 22
- 239000007822 coupling agent Substances 0.000 claims description 20
- 239000003795 chemical substances by application Substances 0.000 claims description 17
- 239000003999 initiator Substances 0.000 claims description 17
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 12
- 238000003848 UV Light-Curing Methods 0.000 claims description 12
- 229920000609 methyl cellulose Polymers 0.000 claims description 11
- 239000001923 methylcellulose Substances 0.000 claims description 11
- 235000010981 methylcellulose Nutrition 0.000 claims description 11
- -1 polyethylene Polymers 0.000 claims description 11
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 9
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 8
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 claims description 6
- 239000003849 aromatic solvent Substances 0.000 claims description 6
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 claims description 6
- JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 claims description 6
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 6
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims description 6
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 claims description 5
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 5
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 5
- 150000002576 ketones Chemical class 0.000 claims description 5
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 claims description 3
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 3
- 239000004593 Epoxy Substances 0.000 claims description 3
- 239000004354 Hydroxyethyl cellulose Substances 0.000 claims description 3
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 claims description 3
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 claims description 3
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 claims description 3
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 claims description 3
- 239000004677 Nylon Substances 0.000 claims description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 3
- 239000004952 Polyamide Substances 0.000 claims description 3
- 239000004698 Polyethylene Substances 0.000 claims description 3
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 3
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 3
- 235000019445 benzyl alcohol Nutrition 0.000 claims description 3
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 3
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 3
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims description 3
- 229920002313 fluoropolymer Polymers 0.000 claims description 3
- 239000004811 fluoropolymer Substances 0.000 claims description 3
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 claims description 3
- 239000001863 hydroxypropyl cellulose Substances 0.000 claims description 3
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 claims description 3
- GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 claims description 3
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 claims description 3
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 3
- 229920001778 nylon Polymers 0.000 claims description 3
- 229920002647 polyamide Polymers 0.000 claims description 3
- 229920000728 polyester Polymers 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- 229920001296 polysiloxane Polymers 0.000 claims description 3
- 229920002635 polyurethane Polymers 0.000 claims description 3
- 239000004814 polyurethane Substances 0.000 claims description 3
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 claims description 3
- 229920002554 vinyl polymer Polymers 0.000 claims description 3
- 239000008096 xylene Substances 0.000 claims description 3
- 230000001476 alcoholic effect Effects 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims description 2
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 claims 1
- 239000005453 ketone based solvent Substances 0.000 claims 1
- 229920005749 polyurethane resin Polymers 0.000 claims 1
- 229910018557 Si O Inorganic materials 0.000 abstract description 2
- 239000005328 architectural glass Substances 0.000 abstract description 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 2
- 239000001257 hydrogen Substances 0.000 abstract description 2
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 abstract description 2
- 238000012795 verification Methods 0.000 abstract description 2
- 238000003756 stirring Methods 0.000 description 20
- 239000010408 film Substances 0.000 description 18
- 239000011259 mixed solution Substances 0.000 description 15
- 238000012360 testing method Methods 0.000 description 11
- 239000000243 solution Substances 0.000 description 10
- 239000005341 toughened glass Substances 0.000 description 8
- 229910000831 Steel Inorganic materials 0.000 description 6
- 239000010959 steel Substances 0.000 description 6
- 238000001816 cooling Methods 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- 238000005728 strengthening Methods 0.000 description 5
- 239000004925 Acrylic resin Substances 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- 239000006087 Silane Coupling Agent Substances 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- 239000004816 latex Substances 0.000 description 3
- 229920000126 latex Polymers 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 229920001084 poly(chloroprene) Polymers 0.000 description 3
- 229920006122 polyamide resin Polymers 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 229920013716 polyethylene resin Polymers 0.000 description 2
- 241001391944 Commicarpus scandens Species 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000005357 flat glass Substances 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000002834 transmittance Methods 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
- 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
- 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
- C03C17/28—Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Composite Materials (AREA)
- Surface Treatment Of Glass (AREA)
- Paints Or Removers (AREA)
Abstract
The invention discloses glass reinforcing liquid, composite chemically strengthened glass and a preparation method thereof. The glass reinforcing liquid is prepared from the following raw materials in parts by weight: 5-10 parts of resin, 15-35 parts of cellulose, 1-4 parts of an auxiliary agent and 5-70 parts of a solvent; the yellowing value of the reinforcing liquid is less than or equal to 0.8, and the adhesive force is 5B. The glass reinforcing liquid can form a film after being solidified on the surface of glass, and the film has a structure similar to an Si-O tetrahedral framework in the glass, so that microcracks on the surface of the glass can be filled, a fracture layer on the surface of the glass is eliminated, the impact resistance of the glass can be greatly improved, and the impact resistance can be improved by 21-58% through experimental verification. Meanwhile, the glass reinforcing liquid can dehydrate with hydroxyl groups on the glass to form stronger covalent bonds which are tens of times larger than the common hydrogen bond energy, so that the glass reinforcing liquid has excellent adhesive force to the glass. The composite chemically strengthened glass can be widely applied to the fields of smart phones, automobiles, architectural glass and the like, and has high commercial value.
Description
Technical Field
The invention relates to the technical field of glass production, in particular to glass reinforcing liquid, composite chemically strengthened glass and a preparation method thereof.
Background
In recent years, the development of touch screen type electronic products is rapid, and the smart phone technology is particularly prominent. With the continuous update and the replacement of intelligent products, the demand of functional glass is increasing, and with the increase of the size of a display screen of a mobile phone, the thickness of the mobile phone is continuously reduced, and the mobile phone glass becomes increasingly thinner, so that the thinning of the mobile phone glass and the touch mode of a touch panel of the mobile phone put forward higher requirements on the strength and the hardness of the glass.
At present, widely used mobile phone glass is single-layer plate glass, microcracks exist on the surface of the processed glass more or less, and the strength of the glass is greatly reduced due to the abrasion, scratch and other flaws on the surface of the glass. In order to improve the impact resistance and the drop resistance of the mobile phone glass, the mobile phone glass is generally subjected to film sticking and glass strengthening treatment. However, the film sticking process on the glass panel is complicated, the cost is increased, the shock resistance is poor, and the glass panel is easy to break and splash due to impact. In addition, the chemically tempered glass has a poor impact resistance, and it has been found through experimental tests that the chemically tempered glass is directly broken when a steel ball with Φ of 32 and M of 130g is freely dropped from a height of 600mm to the chemically tempered glass. That is, the strength of the glass is improved to some extent by the above method, but there is a gap from the desire in the industry for a functional glass having high strength.
Therefore, the development of glasses with higher strength is still an important research direction in the field of glass manufacturing. For thinned glass, applying a coating can be a very effective way to treat the defects. The applicant aims to provide a glass reinforcing liquid which can be coated on the surface of glass to fill the defects on the surface of the glass so as to improve the strength of the glass.
Disclosure of Invention
The technical problem to be solved by the present invention is to provide a glass reinforcing liquid, which can be sprayed on the surface of glass to form a thin film after being cured, and can fill microcracks on the surface of the glass, thereby eliminating a fracture layer on the surface of the glass, greatly improving the impact resistance of the glass, and simultaneously not affecting the warping degree and the light transmittance of the glass.
Another object of the present invention is to provide a method for preparing the glass reinforcing liquid.
Still another object of the present invention is to provide a composite chemically strengthened glass having the glass reinforcing liquid.
The invention also aims to provide a preparation method of the composite chemically strengthened glass.
In order to solve the technical problems, the invention provides a glass reinforcing liquid which is prepared from the following raw materials in parts by weight: 5-10 parts of resin, 15-35 parts of cellulose, 1-4 parts of an auxiliary agent and 5-70 parts of a solvent; the yellowing value of the reinforcing liquid is less than or equal to 0.8, and the adhesive force is 5B.
As a preferable mode of the glass reinforcing liquid of the invention, the resin is made of one or more of the following raw materials: epoxy, polyester, polyurethane, polyamide, acrylic, polyethylene, nylon, fluoropolymer, silicone, polyvinyl acetal, vinyl chloride, vinyl acetate, vinyl alcohol, hydroxyalkyl acrylate. Further preferably, the resin is a polyethylene resin having hydroxyl functional groups. Further preferably, the resin is made from one or more of the following raw materials: vinyl chloride, vinyl acetate, vinyl alcohol, hydroxyalkyl acrylates. More preferably, the molecular weight of the resin is 30000-100000. The molecular weight of the resin is 30000-50000.
As another preferable scheme of the glass reinforcing liquid, the used auxiliary agent comprises an initiator, a coupling agent and a leveling agent, wherein the initiator is 0.4-1.2 w%, the coupling agent is 0.2-1.5 w%, and the leveling agent is 0.3-1.3 w%. Further preferably, the cellulose is one or more of methyl cellulose, hydroxypropyl cellulose, hydroxyethyl cellulose and carboxymethyl cellulose. Further preferably, the cellulose is methyl cellulose.
In still another preferred embodiment of the glass reinforcing liquid of the present invention, the solvent is a mixture of one or more of an ester solvent, an alcohol solvent, a ketone solvent, an aromatic solvent, and a glycol solvent. Further preferably, the ester solvent comprises one or more of n-butyl acetate, ethyl acetate or isobutyl acetate. Further preferably, the alcoholic solvent comprises one or more of isobutanol, ethanol or benzyl alcohol. Further preferably, the ketone solvent includes one or more of methyl isobutyl ketone, methyl ethyl ketone, acetone, or diisobutyl ketone. Further preferably, the aromatic solvent comprises one or more of a naphtha solvent, xylene or toluene. Further preferably, the glycol solvent includes one or more of propylene glycol methyl ether acetate, propylene glycol methyl ether or butylene glycol.
The invention also provides a preparation method of the glass reinforcing liquid, which comprises the following steps:
step S1, adding the resin into the solvent to fully dissolve the resin to obtain an initial solution;
step S2, slowly adding cellulose into the initial solution, and uniformly stirring to obtain a mixed solution;
and step S3, cooling to room temperature, adding an auxiliary agent into the mixed solution, and uniformly stirring to obtain the glass reinforcing liquid.
In a preferred embodiment of the method for preparing the glass reinforcing liquid of the present invention, a magnetic stirrer is used for stirring in step S2, the rotation speed of the magnetic stirrer is 1000 to 2000r/min, and the stirring time is 1 to 2 hours.
In another preferable embodiment of the method for preparing the glass reinforcing liquid of the present invention, in the step S3, the auxiliary agent and the mixed solution are mixed in a mixer, wherein the rotation speed of the mixer is 600 to 800r/min, and the mixing time is 3 to 5 min.
The invention also provides composite chemically strengthened glass, which comprises a chemically strengthened glass substrate and a strengthening film formed by spraying the glass strengthening liquid on the surface of the chemically strengthened glass substrate.
As a preferable scheme of the composite chemically strengthened glass, the thickness of the chemically strengthened glass substrate is 0.6-0.7 mm, and the thickness of the reinforced film is 10-20 um.
The invention also provides a preparation method of the chemically strengthened composite chemically strengthened glass, which comprises the following steps:
spraying the glass reinforcing liquid on the surface of the chemically strengthened glass substrate by using a spray gun, wherein the spraying distance is controlled to be 10-15 cm, and the spraying pressure is controlled to be 0.3-0.5 Mpa;
placing the chemically strengthened glass substrate sprayed with the glass reinforcing liquid in an environment with the temperature of more than or equal to 25 ℃ for standing for a certain time or placing the glass substrate sprayed with the glass reinforcing liquid in an oven with the temperature of 80-120 ℃ for baking for a certain time or carrying out UV curing on the chemically strengthened glass substrate coated with the glass reinforcing liquid, wherein the UV curing energy is 1800-2。
Compared with the prior art, the invention has the following beneficial effects:
1. the glass reinforcing liquid can form a film after being solidified on the surface of glass, and the film has a structure similar to an Si-O tetrahedral framework in the glass, so that microcracks on the surface of the glass can be filled, a fracture layer on the surface of the glass is eliminated, the impact resistance of the glass can be greatly improved, and the impact resistance can be improved by 21-58% through experimental verification.
2. The glass reinforcing liquid and hydroxyl on the glass can be dehydrated to form a stronger covalent bond which is tens of times larger than the common hydrogen bond, so that the glass reinforcing liquid has excellent adhesive force to the glass.
3. The preparation method of the glass reinforcing liquid is simple, easy to operate, environment-friendly and safe.
4. The composite chemically strengthened glass can be widely applied to the fields of smart phones, automobiles, architectural glass and the like, and has high commercial value.
5. The preparation method of the composite chemically strengthened glass is simple to operate and easy for industrial production.
Detailed Description
The invention discloses a glass reinforcing liquid which is prepared from the following raw materials in parts by weight: 5-10 parts of resin, 15-35 parts of cellulose, 1-4 parts of an auxiliary agent and 5-70 parts of a solvent; the yellowing value of the reinforcing liquid is less than or equal to 0.8, and the adhesive force is 5B. .
Preferably, the resin is made from one or more of the following raw materials: epoxy, polyester, polyurethane, polyamide, acrylic, polyethylene, nylon, fluoropolymer, silicone, polyvinyl acetal, vinyl chloride, vinyl acetate, vinyl alcohol, hydroxyalkyl acrylate.
Preferably, the resin is a polyethylene resin having hydroxyl functional groups.
Preferably, the resin is made from one or more of the following raw materials: vinyl chloride, vinyl acetate, vinyl alcohol, hydroxyalkyl acrylates.
Preferably, the molecular weight of the resin is 30000-100000.
Preferably, the molecular weight of the resin is 30000-50000.
Preferably, the used auxiliary agent comprises an initiator, a coupling agent and a flatting agent, wherein the initiator is 0.4-1.2 w%, the coupling agent is 0.2-1.5 w%, and the flatting agent is 0.3-1.3 w%.
Preferably, the cellulose is one or more of methyl cellulose, hydroxypropyl cellulose, hydroxyethyl cellulose and carboxymethyl cellulose
Preferably, the cellulose is methyl cellulose.
Preferably, the solvent is one or more of an ester solvent, an alcohol solvent, a ketone solvent, an aromatic solvent and a glycol solvent.
Preferably, the ester solvent includes one or more of n-butyl acetate, ethyl acetate or isobutyl acetate.
Preferably, one or more of isobutanol, ethanol or benzyl alcohol.
Preferably, the ketone solvent includes one or more of methyl isobutyl ketone, methyl ethyl ketone, acetone, or diisobutyl ketone.
Preferably, the aromatic solvent comprises one or more of a naphtha solvent, xylene, or toluene.
Preferably, the glycol solvent includes one or more of propylene glycol methyl ether acetate, propylene glycol methyl ether or butylene glycol.
The preparation method of the glass reinforcing liquid provided by the invention comprises the following steps:
step S1, adding the resin into the solvent to fully dissolve the resin to obtain an initial solution;
step S2, slowly adding cellulose into the initial solution, and uniformly stirring to obtain a mixed solution;
and step S3, cooling to room temperature, adding an auxiliary agent into the mixed solution, and uniformly stirring to obtain the glass reinforcing liquid.
Preferably, a magnetic stirrer is adopted for stirring in the step S2, the rotating speed of the magnetic stirrer is 1000-2000 r/min, and the stirring time is 1-2 h.
Preferably, in the step S3, the auxiliary agent and the mixed solution are mixed in a mixer, wherein the rotation speed of the mixer is 600-800 r/min, and the mixing time is 3-5 min.
The composite chemically strengthened glass provided by the invention comprises a glass substrate and a strengthening film formed by spraying the glass strengthening liquid provided by the invention on the surface of the glass substrate. Preferably, the thickness of the glass substrate is 0.05-0.7 mm, and the thickness of the reinforced film is 10-20 um.
The preparation method of the composite chemically strengthened glass provided by the invention comprises the following steps: spraying the glass reinforcing liquid as defined in any one of claims 1 to 15 on the surface of a glass substrate by a spray gun, wherein the spraying distance is controlled to be 10 to 15cm, and the spraying pressure is controlled to be 0.3 to 0.5 Mpa; and (2) standing the glass substrate sprayed with the glass reinforcing liquid for 24h in an environment with the temperature of more than or equal to 25 ℃, or baking the glass substrate sprayed with the glass reinforcing liquid in an oven with the temperature of 80-120 ℃ for 30min, or carrying out UV curing on the chemically strengthened glass substrate coated with the glass reinforcing liquid, wherein the UV curing energy is 1800-.
The above-mentioned chemical reagents are commercially available and the equipment used is also commercially available.
In order to more clearly understand the technical features, objects, and effects of the present invention, specific embodiments of the present invention will now be described in detail. It is to be understood that the described embodiments are merely exemplary of the invention, and not restrictive of the full scope of the invention. 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: glass reinforcing liquid A and preparation thereof
The glass reinforcing liquid A provided by the embodiment is prepared from the following raw materials in parts by weight: 5 parts of resin, 15 parts of cellulose, 1 part of auxiliary agent and 5 parts of solvent. Wherein the resin is epoxy resin 3 parts, polyamide resin 1 parts, acrylic resin 1, and its molecular weight is 30000. The cellulose is methyl cellulose. The auxiliary agent comprises an initiator, a coupling agent and a flatting agent, wherein the initiator is 0.4 w%, the coupling agent is 0.2 w%, and the flatting agent is 0.3 w%. The initiator is neoprene latex, and the coupling agent is aluminum-titanium-boron-titanium composite coupling agent or silane coupling agent. The leveling agent is butyl cellulose.
The preparation steps are as follows:
step S1, adding the resin into the solvent to fully dissolve the resin to obtain an initial solution;
step S2, slowly adding cellulose into the initial solution, and uniformly stirring to obtain a mixed solution; in the step, a magnetic stirrer is adopted for stirring, the rotating speed of the magnetic stirrer is 1000/min, and the stirring time is 2 hours.
And step S3, cooling to room temperature, adding an auxiliary agent into the mixed solution, and uniformly stirring to obtain the glass reinforcing liquid. In the step, the auxiliary agent and the mixed solution are mixed in a mixer, wherein the rotating speed of the mixer is 800r/min, and the mixing time is 3 min.
Example 2: glass reinforcing liquid B and preparation thereof
The glass reinforcing liquid B provided by the embodiment is prepared from the following raw materials in parts by weight: 10 parts of resin, 35 parts of cellulose, 4 parts of auxiliary agent and 70 parts of solvent. Wherein the resin is 3 parts of epoxy resin, 3 parts of polyamide resin and 6 parts of acrylic resin, and the molecular weight of the resin is 100000. The cellulose is methyl cellulose. The auxiliary agent comprises an initiator, a coupling agent and a flatting agent, and the cellulose is methyl cellulose. The auxiliary agent comprises an initiator, a coupling agent and a flatting agent, wherein the initiator is 0.4 w%, the coupling agent is 0.2 w%, and the flatting agent is 0.3 w%. The initiator is neoprene latex, and the coupling agent is aluminum-titanium-boron-titanium composite coupling agent or silane coupling agent. The leveling agent is butyl cellulose.
The preparation steps are as follows:
step S1, adding the resin into the solvent to fully dissolve the resin to obtain an initial solution;
step S2, slowly adding cellulose into the initial solution, and uniformly stirring to obtain a mixed solution; in the step, a magnetic stirrer is adopted for stirring, the rotating speed of the magnetic stirrer is 2000/min, and the stirring time is 2 hours.
And step S3, cooling to room temperature, adding an auxiliary agent into the mixed solution, and uniformly stirring to obtain the glass reinforcing liquid. In the step, the auxiliary agent and the mixed solution are mixed in a mixer, wherein the rotating speed of the mixer is 600r/min, and the mixing time is 5 min.
Example 3: glass reinforcing liquid C and preparation thereof
The glass reinforcing liquid C provided in this example is prepared from the following raw materials in parts by weight: 7.5 parts of resin, 25 parts of cellulose, 3 parts of auxiliary agent and 35 parts of solvent. Wherein the resin comprises 2 parts of epoxy resin, 3 parts of polyamide resin and 2.5 parts of acrylic resin, and the molecular weight of the resin is 80000. The cellulose is methyl cellulose. The auxiliary agent comprises an initiator, a coupling agent and a flatting agent, and the cellulose is methyl cellulose. The auxiliary agent comprises an initiator, a coupling agent and a flatting agent, wherein the initiator is 0.4 w%, the coupling agent is 0.2 w%, and the flatting agent is 0.3 w%. The initiator is neoprene latex, and the coupling agent is aluminum-titanium-boron-titanium composite coupling agent or silane coupling agent. The leveling agent is butyl cellulose.
The preparation steps are as follows:
step S1, adding the resin into the solvent to fully dissolve the resin to obtain an initial solution;
step S2, slowly adding cellulose into the initial solution, and uniformly stirring to obtain a mixed solution; in the step, a magnetic stirrer is adopted for stirring, the rotating speed of the magnetic stirrer is 1500r/min, and the stirring time is 1.5 h.
And step S3, cooling to room temperature, adding an auxiliary agent into the mixed solution, and uniformly stirring to obtain the glass reinforcing liquid. In the step, the auxiliary agent and the mixed solution are mixed in a mixer, wherein the rotating speed of the mixer is 700r/min, and the mixing time is 4 min.
Example 4: composite chemically strengthened glass A and preparation thereof
The composite chemically strengthened glass a provided by the present embodiment includes a chemically strengthened glass substrate and a reinforcing film formed by spraying a glass reinforcing liquid a on a surface of the glass substrate. The thickness of the glass substrate is 0.55mm, and the thickness of the reinforced film is 20 um.
The preparation steps are as follows:
spraying the glass reinforcing liquid A on the surface of a glass substrate by using a manual air spray gun, wherein the spraying distance is controlled to be 10cm, and the spraying pressure is controlled to be 0.3 Mpa; placing the glass substrate sprayed with the glass reinforcing liquid in an environment with the temperature of more than or equal to 25 ℃ for standing for 24h, or placing the glass substrate sprayed with the glass reinforcing liquid in an oven with the temperature of 80 ℃ for baking for 30min, or carrying out UV curing on the chemically strengthened glass substrate coated with the glass reinforcing liquid, wherein the UV curing energy is 1800-2。
Example 5: composite chemically strengthened glass B and preparation thereof
The composite chemically strengthened glass B provided in this embodiment includes a chemically strengthened glass substrate and a reinforcing film formed by spraying a glass reinforcing liquid B onto a surface of the glass substrate. The thickness of glass substrate is 2mm, the thickness of reinforcing film is 15 um.
The preparation steps are as follows:
spraying the glass reinforcing liquid B on the surface of the glass substrate by using a manual air spray gun, wherein the spraying distance is controlled to be 15cm, and the spraying pressure is controlled to be 0.5 Mpa; placing the glass substrate sprayed with the glass reinforcing liquid in an environment with the temperature of more than or equal to 30 ℃ for standing for 24h or placing the glass substrate sprayed with the glass reinforcing liquid in a 120 ℃ oven for baking 30min or performing UV curing on the chemically strengthened glass substrate coated with the glass reinforcing liquid, wherein the UV curing energy is 1800-2。
Example 6: composite chemically strengthened glass C and preparation thereof
The composite chemically strengthened glass C provided in this embodiment includes a chemically strengthened glass substrate and a reinforcing film formed by spraying a glass reinforcing liquid C onto a surface of the glass substrate. The thickness of the glass substrate is 1.0mm, and the thickness of the reinforced film is 15 um.
The preparation steps are as follows:
spraying the glass reinforcing liquid C on the surface of the glass substrate by using a manual air spray gun, wherein the spraying distance is controlled to be 10cm, and the spraying pressure is controlled to be 0.4 Mpa; placing the glass substrate sprayed with the glass reinforcing liquid in an environment with the temperature of more than or equal to 28 ℃ for standing for 24h, or placing the glass substrate sprayed with the glass reinforcing liquid in an oven with the temperature of 100 ℃ for baking for 30min, or carrying out UV curing on the chemically strengthened glass substrate coated with the glass reinforcing liquid, wherein the UV curing energy is 1800-2。
And (3) detecting the yellowing value and the adhesion force:
the yellowing value detection method comprises the following steps: the yellowing test was performed using astm g154.16 test standard.
The adhesive force detection method comprises the following steps: and spraying glass reinforcing liquid on the surface of the chemically strengthened glass to form a layer of reinforcing film on the surface of the chemically strengthened glass, so as to obtain a sample (refer to the preparation method of the composite chemically strengthened glass). Then horizontally placing the sample, vertically and horizontally marking 10 lines on the surface of the reinforced film at intervals of about 1mm for 100 grids, and quickly pulling up the reinforced film after being adhered by an adhesive tape; the edge of the reinforced film cut is largely fallen off or some squares are partially or completely fallen off, and the falling area is more than 65 percent and is 0B; the edge of the cut falls off in large pieces or some squares partially or completely, and the falling area is more than 35 percent but not more than 65 percent, and is 1B; the edge of the cut falls off in large pieces or some squares partially or completely, and the falling area is more than 15 percent, but not more than 35 percent, the falling area is 2B; the edges or the intersections of the cuts are peeled off, and the peeling area is more than 5 percent but not more than 15 percent and is 3B; the small pieces are peeled off at the intersection of the cuts, and the actual damage in the scribing region is not more than 5 percent and is 4B; the edges of the cuts were completely smooth, and the edges of the grid did not have any flaking of 5B.
Yellowing value | Adhesion force | |
Glass reinforcing liquid A | 0.63 | 5B |
Glass reinforcing liquid B | 0.47 | 5B |
Glass reinforcing liquid C | 0.67 | 5B |
Strength test experiments:
the same steel ball drop test was performed using uncoated conventional tempered glass, composite chemically tempered glass a, composite chemically tempered glass B, and composite chemically tempered glass C having the same length, width, and height dimensions. The experimental process of the composite chemically strengthened glass A is taken as an example for explanation: placing the composite chemically strengthened glass A on a horizontal platform, placing steel balls with phi of 32mm and m of 130 +/-1 g at different heights right above the composite chemically strengthened glass A, enabling the steel balls to freely fall to the surface of the composite chemically strengthened glass A, and observing whether the composite chemically strengthened glass A is cracked. The falling height of the steel ball is increased from 50cm, then 10cm, 20cm, 30cm and 40cm are sequentially increased, and then the height is increased by 5cm until the composite chemically strengthened glass A is cracked. In the test process, a steel ball drop test is respectively carried out on 10 pieces of uncoated conventional tempered glass, 10 pieces of composite chemically strengthened glass A, 10 pieces of composite chemically strengthened glass B and 10 pieces of composite chemically strengthened glass C, so that the reliability of the test result is ensured. The test results are shown in the following table:
transparency test experiment:
the conventional transparency test method is used for carrying out transparency test on the composite chemically strengthened glass A, the composite chemically strengthened glass B and the composite chemically strengthened glass C, and the results show that the transparency of the composite chemically strengthened glass A, the composite chemically strengthened glass B and the composite chemically strengthened glass C is as high as 86-90%.
While embodiments of the present invention have been described, the present invention is not limited to the above-described embodiments, which are intended to be illustrative rather than limiting, and many modifications may be made by those skilled in the art without departing from the spirit and the scope of the invention as defined by the appended claims.
Claims (13)
1. The glass reinforcing liquid is characterized by being prepared from the following raw materials in parts by weight: 5-10 parts of resin, 15-35 parts of cellulose, 1-4 parts of an auxiliary agent and 5-70 parts of a solvent; the yellowing value of the reinforcing liquid is less than or equal to 0.8, and the adhesive force is 5B.
2. The glass reinforcing solution of claim 1, wherein the resin is made from one or more of the following raw materials: epoxy, polyester, polyurethane, polyamide, acrylic, polyethylene, nylon, fluoropolymer, silicone, polyvinyl acetal, vinyl chloride, vinyl acetate, vinyl alcohol, hydroxyalkyl acrylate.
3. The glass-reinforcing liquid of claim 2, wherein the resin is a polyurethane resin having hydroxyl functional groups; the molecular weight of the resin is 30000-100000.
4. The glass-reinforcing liquid according to claim 3, wherein the resin has a molecular weight of 30000 to 100000.
5. The glass-reinforcing liquid according to claim 4, wherein the resin has a molecular weight of 30000 to 50000.
6. The glass reinforcing liquid according to claim 1, wherein the auxiliary agents include an initiator, a coupling agent and a leveling agent, wherein the initiator is 0.4-1.2 w%, the coupling agent is 0.2-1.5 w%, and the leveling agent is 0.3-1.3 w%.
7. The glass reinforcing solution of claim 1, wherein the cellulose is a mixture of one or more of methyl cellulose, hydroxypropyl cellulose, hydroxyethyl cellulose, and carboxymethyl cellulose.
8. The glass reinforcing solution of claim 7, wherein the cellulose is methyl cellulose.
9. The glass reinforcing liquid according to claim 1, wherein the solvent is a mixture of one or more of an ester solvent, an alcohol solvent, a ketone solvent, an aromatic solvent, or a glycol solvent; the ester solvent comprises one or more of n-butyl acetate, ethyl acetate or isobutyl acetate; the alcoholic solvent comprises one or more of isobutanol, ethanol or benzyl alcohol.
10. The glass-reinforcing liquid of claim 9, wherein the ketone-based solvent includes one or more of methyl isobutyl ketone, methyl ethyl ketone, acetone, or diisobutyl ketone; the aromatic solvent comprises one or more of naphtha solvent, xylene or toluene; the glycol solvent comprises one or more of propylene glycol methyl ether acetate, propylene glycol methyl ether or butanediol.
11. A composite chemically strengthened glass comprising a chemically strengthened glass substrate having opposed inner and outer surfaces and a reinforcing film formed by spraying the glass reinforcing solution of any one of claims 1 to 10 onto the inner surface of the chemically strengthened glass substrate.
12. The composite chemically strengthened glass according to claim 11, wherein the glass substrate has a thickness of 0.6 to 0.7mm, and the reinforcing film has a thickness of 10 to 20 um.
13. A method of making a composite chemically strengthened glass according to any one of claims 11 to 12, wherein the method comprises the steps of:
coating the glass reinforcing solution of any one of claims 1-10 on an inner surface of a chemically strengthened glass substrate;
placing the chemically strengthened glass substrate coated with the glass reinforcing liquid in an environment with the temperature of more than or equal to 25 ℃ for standing for a certain time, or placing the chemically strengthened glass substrate coated with the glass reinforcing liquid in an oven with the temperature of 80-120 ℃ for baking for 5-8min, or carrying out UV curing on the chemically strengthened glass substrate coated with the glass reinforcing liquid, wherein the UV curing energy is 1800-2。
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