1. The mercapto-containing organic silicon modified styrene-acrylic emulsion is characterized by being prepared from the following components in parts by mass:

2. the mercapto silicone-modified styrene-acrylic emulsion according to claim 1, wherein the mercapto silicone-modified styrene-acrylic emulsion has the following structure:

wherein R is:

wherein R is₁Represents Me (methyl) or Et (ethyl), R₂、R₃Represents alkyl, R₄Represents H or Me (methyl).

3. The mercapto silicone-modified styrene-acrylic emulsion according to claim 1, wherein the mercapto silicone has a structure shown below:

wherein R is₁Represents Me (methyl) or Et (ethyl).

4. The mercapto silicone-modified styrene-acrylic emulsion according to any one of claims 1 to 3, wherein the mercapto silicone is prepared by:

stirring and heating 100 parts by mass of hydroxyl silicone oil, 1-4 parts by mass of a coupling agent containing mercapto silane, 1-4 parts by mass of a catalyst and 0.5-1 part by mass of deionized water under the protection of nitrogen to 60-70 ℃ for reaction for 10-20 minutes, then heating to 80-100 ℃ for reaction for 2-8 hours, then heating to 110-160 ℃ for reaction for 0.5-3 hours, and carrying out rotary evaporation to obtain the organosilicon containing mercapto.

5. The mercapto-containing silicone-modified styrene-acrylic emulsion according to claim 1, wherein the (meth) acrylic ester is at least one of methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, pentyl (meth) acrylate, hexyl (meth) acrylate, isooctyl (meth) acrylate, lauryl (meth) acrylate, tetradecyl (meth) acrylate, and hexadecyl (meth) acrylate.

6. The mercapto silicone-modified styrene-acrylic emulsion according to claim 1, wherein the (meth) acrylic acid is at least one of methacrylic acid and acrylic acid.

7. The mercapto-containing silicone-modified styrene-acrylic emulsion according to claim 1, wherein the emulsifier is at least one of polyoxyethylene octylphenol ether-10 and sodium lauryl sulfate.

8. The mercapto silicone-modified styrene-acrylic emulsion according to claim 7, wherein when the emulsifier is a composite emulsifier comprising polyoxyethylene octylphenol ether-10 and sodium lauryl sulfate, the mass ratio of the polyoxyethylene octylphenol ether-10 to the sodium lauryl sulfate is (2:1) - (3: 1).

9. The preparation method of the mercapto-containing organic silicon modified styrene-acrylic emulsion is characterized by comprising the following steps:

(1) preparing styrene-acrylic emulsion: adding 1-5 parts by mass of an emulsifier into 100-150 parts by mass of deionized water, and uniformly stirring to obtain an emulsion; uniformly mixing 100 parts by mass of (methyl) acrylate, 3-20 parts by mass of styrene, 1-4 parts by mass of (methyl) acrylic acid and 0.5-30 parts by mass of mercapto-containing organic silicon, dropwise adding the mixture into the emulsion, and dispersing at high speed for 0.5-2 hours to obtain a styrene-acrylic emulsion;

(2) preparation of initiator dilution solution: dissolving 0.5-5 parts by mass of an initiator in 30-90 parts by mass of deionized water to obtain an initiator diluted solution;

(3) preparing an auxiliary agent diluted solution, namely dissolving 0.4-1 part by mass of an auxiliary agent in 20-60 parts by mass of deionized water to obtain an auxiliary agent diluted solution;

(4) adding the 1/4-1/3 mass styrene-acrylic emulsion prepared in the step (1) and the 1/5-2/5 initiator diluted solution prepared in the step (2) into the auxiliary agent diluted solution prepared in the step (3), stirring and heating to 55-85 ℃ for reaction for 0.5-2 hours, dropwise adding the rest of the styrene-acrylic emulsion and the initiator diluted solution for 1-3 hours, reacting for 0.5-1 hour after dropwise adding is completed, adjusting the pH to 6-8 with ammonia water, stopping heating, and sieving to obtain the sulfydryl-containing organic silicon modified styrene-acrylic emulsion.

10. The application of mercapto organosilicon modified styrene-acrylic emulsion in household decoration, paper, leather assistant and other daily use articles.

Background

The water-based paint is used as an environment-friendly green paint, and water is used for replacing the traditional organic solvent in the production process, so that the paint cost can be reduced, the emission of volatile organic compounds can be greatly reduced in practical application, and the harm to human bodies is reduced. The styrene-acrylic emulsion serving as a basic raw material of a typical environment-friendly coating has the advantages of low toxicity, low price, good bonding property and the like, and not only is a good interior decoration coating, but also can be used for special treatment of daily necessities such as paper, leather and the like. However, the traditional styrene-acrylic emulsion has some defects, such as poor stability of the synthesized emulsion, poor water resistance after film formation, insufficient flexibility, film formation cracking and the like. Therefore, the development of a styrene-acrylic emulsion with higher stability, better film-forming water resistance and better flexibility is urgently needed.

The organosilicon has lower surface energy, chain flexibility, water resistance, chemical resistance, physical stability and the like, so that the organosilicon is widely applied to various resins for coatings and shows a plurality of excellent special properties. At present, the modification methods of styrene-acrylic emulsion are many, and can be divided into two categories of physical blending and chemical modification. The physical blending means that organosilicon, organofluorine or other functional monomers with performance complementary to that of the styrene-acrylic emulsion are added to improve the defects, wherein the organosilicon is a common modifier, but the composite emulsion obtained by the physical blending method has poor compatibility and a less ideal modification effect because the styrene-acrylic copolymer and the modified material do not form chemical bond linkage. The chemical modification is generally carried out by copolymerizing a small-molecular organic silicon coupling agent into a styrene-acrylic polymer main chain, namely the general modification method called 'silicone-acrylic emulsion' on the market, wherein the modification method can improve the water resistance of the emulsion, but has the problems of silane hydrolysis and the like, the emulsion stability is not high enough, and the performance improvement is limited.

Disclosure of Invention

The invention aims to provide a sulfydryl-containing organic silicon modified styrene-acrylic emulsion to solve the problems of poor stability, poor film-forming water resistance and flexibility and the like of the traditional styrene-acrylic emulsion. The invention firstly adopts silane coupling agent containing sulfhydryl group to functionalize organic silicon, and then connects the organic silicon on a molecular chain of styrene-acrylic copolymer through the chain transfer function of sulfhydryl group. The introduction of the mercapto-containing organosilicon can increase the stability of the styrene-acrylic emulsion to a certain extent, increase the molecular weight of the styrene-acrylic emulsion and increase the water resistance and flexibility of the styrene-acrylic emulsion. The styrene-acrylic emulsion modified by the organosilicon containing the sulfhydryl group synthesized by the method can be used as raw materials in the aspects of home decoration, paper, leather auxiliaries and the like.

The second purpose of the invention is to provide a preparation method of the mercapto-containing organosilicon modified styrene-acrylic emulsion.

The third purpose of the invention is to provide the application of the mercapto-containing organosilicon modified styrene-acrylic emulsion.

The primary purpose of the invention is realized by the following technical scheme:

the mercapto-containing organic silicon modified styrene-acrylic emulsion is prepared from the following components in parts by mass:

further, the structure of the mercapto-containing organosilicon modified styrene-acrylic emulsion is as follows:

wherein R is:

wherein R is₁Represents Me (methyl) or Et (ethyl), R₂、R₃Represents alkyl, R₄Represents H or Me (methyl).

Further, the structure of the mercapto-containing organosilicon is shown as follows:

wherein R is₁Represents Me (methyl) or Et (ethyl).

Further, the mercapto-containing organosilicon can be prepared by the following method:

stirring and heating 100 parts by mass of hydroxyl silicone oil, 1-4 parts by mass of a coupling agent containing mercapto silane, 1-4 parts by mass of a catalyst and 0.5-1 part by mass of deionized water under the protection of nitrogen to 60-70 ℃ for reaction for 10-20 minutes, then heating to 80-100 ℃ for reaction for 2-8 hours, then heating to 110-160 ℃ for reaction for 0.5-3 hours, and carrying out rotary evaporation to obtain the organosilicon containing mercapto.

Further, the molecular weight of the hydroxyl silicone oil is 500-10000.

Further, the mercapto silane coupling agent is at least one of 3-mercaptopropylmethyldiethoxysilane, 3-mercaptopropylmethyldimethoxysilane and 3-mercaptopropylethyldiethoxysilane.

Further, the catalyst is a quaternary ammonium salt;

further, the quaternary ammonium salt is tetramethylammonium hydroxide.

Further, the (meth) acrylic ester is at least one of methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, pentyl (meth) acrylate, hexyl (meth) acrylate, isooctyl (meth) acrylate, lauryl (meth) acrylate, tetradecyl (meth) acrylate, and hexadecyl (meth) acrylate.

Further, the (meth) acrylic acid is at least one of methacrylic acid and acrylic acid.

Further, the emulsifier is at least one of polyoxyethylene octyl phenol ether-10 and sodium dodecyl sulfate.

Further, when the emulsifier is a composite emulsifier composed of polyoxyethylene octyl phenol ether-10 and sodium dodecyl sulfate, the mass ratio of the polyoxyethylene octyl phenol ether-10 to the sodium dodecyl sulfate is (2:1) - (3: 1).

Further, the auxiliary agent is a phosphate buffer.

Further, the phosphate buffer is any one of sodium hydrogen phosphate, disodium hydrogen phosphate, and dipotassium hydrogen phosphate.

Further, the phosphate buffer is disodium phosphate.

Further, the initiator is any one of ammonium persulfate and potassium persulfate.

The second purpose of the invention is realized by the following technical scheme:

a preparation method of sulfydryl-containing organic silicon modified styrene-acrylic emulsion comprises the following steps:

(1) preparing styrene-acrylic emulsion: adding 1-5 parts by mass of an emulsifier into 100-150 parts by mass of deionized water, and uniformly stirring to obtain an emulsion; uniformly mixing 100 parts by mass of (methyl) acrylate, 3-20 parts by mass of styrene, 1-4 parts by mass of (methyl) acrylic acid and 0.5-30 parts by mass of mercapto-containing organic silicon, dropwise adding the mixture into the emulsion, and dispersing at high speed for 0.5-2 hours to obtain a styrene-acrylic emulsion;

(2) preparation of initiator dilution solution: dissolving 0.5-5 parts by mass of an initiator in 30-90 parts by mass of deionized water to obtain an initiator diluted solution;

(3) preparing an auxiliary agent diluted solution, namely dissolving 0.4-1 part by mass of an auxiliary agent in 20-60 parts by mass of deionized water to obtain an auxiliary agent diluted solution;

(4) adding the 1/4-1/3 mass styrene-acrylic emulsion prepared in the step (1) and the 1/5-2/5 initiator diluted solution prepared in the step (2) into the auxiliary agent diluted solution prepared in the step (3), stirring and heating to 55-85 ℃ for reaction for 0.5-2 hours, dropwise adding the rest of the styrene-acrylic emulsion and the initiator diluted solution for 1-3 hours, reacting for 0.5-1 hour after dropwise adding is completed, adjusting the pH to 6-8 with ammonia water, stopping heating, and sieving to obtain the sulfydryl-containing organic silicon modified styrene-acrylic emulsion.

The third purpose of the invention is realized by the following technical scheme:

the application of mercapto organosilicon modified styrene-acrylic emulsion in household decoration, paper, leather assistant and other daily use articles.

The concrete application is as follows: coating the mercapto-containing organic silicon modified styrene-acrylic emulsion on the surface of a base material, and drying water at the temperature of 30-80 ℃ to form a film.

Compared with the prior art, the invention has the following advantages and effects:

(1) the invention provides a sulfydryl-containing organic silicon modified styrene-acrylic emulsion, which adopts sulfydryl-containing functionalized macromolecular organic silicon and successfully grafts the organic silicon on a molecular chain of the styrene-acrylic emulsion by utilizing the chain transfer function of sulfydryl. Compared with the traditional physical mixing, the chemical modification has certain advantages, is different from the modification of a micromolecular organosilane coupling agent, and provides a new route for modifying styrene-acrylic emulsion by organic silicon.

(2) Aiming at the problems of poor water resistance and poor mechanical flexibility of the traditional styrene-acrylic emulsion, the invention adopts the sulfydryl-containing organic silicon with small surface energy and good hydrophobicity for chemical compounding, so that the modified coating has the characteristics of excellent water resistance, flexibility and the like, the water absorption can be reduced to about 2.7 percent, and the elongation at break can reach about 593 percent.

(3) The organic silicon modified phenyl propylene emulsion containing the sulfhydryl group, which is obtained by the invention, is used as a raw material of the coating, has the advantages of green and pollution-free property, high coating quality, convenient construction and the like, can be used as a raw material for special treatment of daily necessities such as paper, leather and the like.

Drawings

FIG. 1 is a nuclear magnetic hydrogen spectrum of organosilicon containing mercapto group.

Detailed Description

The present invention will be described in further detail with reference to examples, but the embodiments of the present invention are not limited thereto.

The emulsion stability and film forming performance test of the invention is carried out according to the following test methods or standards:

appearance of the emulsion: dipping the emulsion with a glass rod, and then lifting and observing the color, the uniformity, the transparency and the flowing state of the emulsion. The blue light of the emulsion color indicates that the emulsion particle size is smaller and the emulsion is more stable; when the emulsion is milky white, the particle size of the emulsion is larger than 100 nm.

Solid content of the emulsion: weighing part of the emulsion, completely drying at 120 ℃, cooling to room temperature, and taking the rest nonvolatile components as the percentage of the total emulsion by mass.

Centrifugal stability: the storage stability of the emulsion was simulated by using a centrifugation accelerated precipitation experiment. The emulsion is acted for 30min at the rotating speed of 3000r/min, and whether the emulsion has the phenomena of precipitation, delamination, flocculation and the like is observed. If not, the emulsion has better storage stability.

Calcium ion stability: according to the GB/T20623-2006 standard, 5mL of finished emulsion and 1mL of calcium chloride solution with the mass fraction of 0.5% are added into a beaker, stirred uniformly and placed in a 10mL sample bottle, and after the sample bottle is placed in the shade for 48 hours, whether the phenomena of layering, precipitation, flocculation and the like occur or not is observed.

Water contact angle: the contact angle of distilled water on the surface of the coating film was measured using a contact angle measuring instrument, and all measurements were carried out at 25 ℃.

The film adhesion was determined according to GB/T9286-1998.

Water resistance was determined as described in GB/1733-1993.

The mechanical properties were determined according to GB/T528-2009.

Example 1

(1) Preparation of mercapto-containing silicone: 100 parts by mass of hydroxyl silicone oil (molecular weight is about 2000), 1.5 parts by mass of 3-mercaptopropyl-methyldimethoxysilane, 2 parts by mass of tetramethylammonium hydroxide and 0.5 part by mass of deionized water are added into a reactor provided with a reflux condenser tube and a stirrer, and nitrogen is introduced for protection in the whole reaction process. Heating and stirring to 75 ℃, reacting for 10 minutes, then heating to 95 ℃, reacting for 5 hours, heating to 150 ℃, removing reflux condensation, and reacting for 30After the reaction is finished, transferring the mixture into a rotary evaporator, and carrying out rotary evaporation for 3 hours at 120 ℃ to obtain the organic silicon containing sulfydryl. FIG. 1 shows PMMS of organosilicon containing sulfhydryl group¹An H NMR spectrum showed a hydrogen proton peak of — SH near δ 1.23.

(2) Preparing the mercapto-containing organic silicon modified styrene-acrylic emulsion: adding 3 parts by mass of polyoxyethylene octyl phenol ether-10, 2 parts by mass of sodium dodecyl sulfate and 120 parts by mass of deionized water into a three-neck flask, and stirring at room temperature until the mixture is dissolved to obtain an emulsion. And uniformly mixing 60 parts by mass of butyl acrylate, 40 parts by mass of methyl methacrylate, 10 parts by mass of styrene, 2 parts by mass of acrylic acid and 2 parts by mass of organosilicon containing mercapto group in a beaker, dropwise adding the mixture into the emulsion, and dispersing the mixture at a high speed for 0.5 hour to obtain the styrene-acrylic emulsion.

1 part by mass of potassium persulfate was dissolved in 80 parts by mass of deionized water to obtain an initiator diluted solution. 0.6 part by mass of disodium hydrogenphosphate dodecahydrate was dissolved in 50 parts by mass of deionized water to obtain a buffer diluted solution. Adding 1/3 mass of styrene-acrylic emulsion into a three-neck flask with a condensing reflux and a stirring rod, adding 2/5 of the initiator diluted solution, adding the buffer diluted solution, stirring and heating to 75 ℃ for reaction for 1 hour.

And uniformly dropwise adding the rest styrene-acrylic emulsion and the initiator diluted solution for about 2 hours, reacting for 30 minutes, and enabling the emulsion to generate a blue light phenomenon in the process. And finally, adjusting the pH to 6-8 with ammonia water, stopping the reaction, and filtering with 200-mesh filter cloth to obtain the sulfydryl-containing organic silicon modified styrene-acrylic emulsion.

(3) Coating of the mercapto-containing organosilicon styrene-acrylic emulsion: and (3) coating the obtained styrene-acrylic coating on the surface of a clean glass sheet, and drying the glass sheet at 40 ℃ for 6 hours.

The results of the stability test of the styrene-acrylic emulsion obtained in this example are shown in Table 1.

The results of the performance tests of the styrene-acrylic emulsion coating film obtained in this example are shown in Table 2.

Example 2

(1) Preparation of mercapto-containing silicone: 100 parts by mass of hydroxyl silicone oil (molecular weight is about 2000), 4 parts by mass of 3-mercaptopropyl-methyldimethoxysilane, 2 parts by mass of tetramethylammonium hydroxide and 0.5 part by mass of deionized water are added into a reactor provided with a reflux condenser tube and a stirrer, and nitrogen is introduced for protection in the whole reaction process. Heating and stirring to 75 ℃, reacting for 10 minutes, then heating to 95 ℃, reacting for 5 hours, heating to 150 ℃, removing reflux condensation, reacting for 1 hour, transferring into a rotary evaporator, and carrying out rotary evaporation at 120 ℃ for 3 hours to obtain the organic silicon containing sulfydryl.

(2) Preparing the mercapto-containing organic silicon modified styrene-acrylic emulsion: adding 3 parts by mass of polyoxyethylene octyl phenol ether-10, 1 part by mass of sodium dodecyl sulfate and 130 parts by mass of deionized water into a three-neck flask, and stirring at room temperature until the mixture is dissolved to obtain an emulsion. And uniformly mixing 70 parts by mass of butyl acrylate, 30 parts by mass of methyl methacrylate, 20 parts by mass of styrene, 2 parts by mass of acrylic acid and 6 parts by mass of mercapto-containing organic silicon in a beaker, dropwise adding the mixture into the emulsion, and dispersing the mixture at a high speed for 0.5 hour to obtain the styrene-acrylic emulsion.

3 parts by mass of potassium persulfate was dissolved in 90 parts by mass of deionized water to obtain an initiator diluted solution. 0.4 part by mass of disodium hydrogenphosphate dodecahydrate was dissolved in 40 parts by mass of deionized water to obtain a buffer diluted solution. Adding 1/3 mass of styrene-acrylic emulsion into a three-neck flask with a condensing reflux and a stirring rod, adding 2/5 of the initiator diluted solution, adding the buffer diluted solution, stirring and heating to 75 ℃ for reaction for 1 hour.

And uniformly dropwise adding the rest styrene-acrylic emulsion and the initiator diluted solution for about 2 hours, reacting for 30 minutes, and enabling the emulsion to generate a blue light phenomenon in the process. And finally, adjusting the pH to 6-8 with ammonia water, stopping the reaction, and filtering with 200-mesh filter cloth to obtain the sulfydryl-containing organic silicon modified styrene-acrylic emulsion.

(3) Coating of the mercapto-containing organosilicon styrene-acrylic emulsion: and (3) coating the obtained styrene-acrylic coating on the surface of a clean glass sheet, and drying the glass sheet at 40 ℃ for 6 hours.

The results of the stability test of the styrene-acrylic emulsion obtained in this example are shown in Table 1.

The results of the performance tests of the styrene-acrylic emulsion coating film obtained in this example are shown in Table 2.

Example 3

(1) Preparation of mercapto-containing silicone: 100 parts by mass of hydroxyl silicone oil (molecular weight is about 600), 2 parts by mass of 3-mercaptopropyl-methyldimethoxysilane, 2 parts by mass of tetramethyl ammonium hydroxide and 0.5 part by mass of deionized water are added into a reactor provided with a reflux condenser tube and a stirrer, and nitrogen is introduced for protection in the whole reaction process. Heating and stirring to 75 ℃, reacting for 10 minutes, then heating to 95 ℃, reacting for 5 hours, heating to 150 ℃, removing reflux condensation, reacting for 30 minutes, transferring into a rotary evaporator, and carrying out rotary evaporation at 120 ℃ for 3 hours to obtain the organic silicon containing sulfydryl.

(2) Preparing the mercapto-containing organic silicon modified styrene-acrylic emulsion: adding 3 parts by mass of polyoxyethylene octyl phenol ether-10, 2 parts by mass of sodium dodecyl sulfate and 150 parts by mass of deionized water into a three-neck flask, and stirring at room temperature until the mixture is dissolved to obtain an emulsion. And uniformly mixing 60 parts by mass of ethyl acrylate, 40 parts by mass of methyl methacrylate, 15 parts by mass of styrene, 4 parts by mass of acrylic acid and 12 parts by mass of mercapto-containing organosilicon in a beaker, dropwise adding the mixture into the emulsion, and dispersing the mixture at a high speed for 0.5 hour to obtain the styrene-acrylic emulsion.

2 parts by mass of potassium persulfate was dissolved in 70 parts by mass of deionized water to obtain an initiator diluted solution. 0.8 part by mass of disodium hydrogenphosphate dodecahydrate was dissolved in 50 parts by mass of deionized water to obtain a buffer diluted solution. Adding 1/3 mass of styrene-acrylic emulsion into a three-neck flask with a condensing reflux and a stirring rod, adding 2/5 of the initiator diluted solution, adding the buffer diluted solution, stirring and heating to 75 ℃ for reaction for 1 hour.

And uniformly dropwise adding the rest styrene-acrylic emulsion and the initiator diluted solution for about 2 hours, reacting for 30 minutes, and enabling the emulsion to generate a blue light phenomenon in the process. And finally, adjusting the pH to 6-8 with ammonia water, stopping the reaction, and filtering with 200-mesh filter cloth to obtain the sulfydryl-containing organic silicon modified styrene-acrylic emulsion.

(3) Coating of the mercapto-containing organosilicon styrene-acrylic emulsion: and (3) coating the obtained styrene-acrylic coating on the surface of a clean glass sheet, and drying the glass sheet at 40 ℃ for 6 hours.

The results of the stability test of the styrene-acrylic emulsion obtained in this example are shown in Table 1.

The results of the performance tests of the styrene-acrylic emulsion coating film obtained in this example are shown in Table 2.

Example 4

(1) Preparation of mercapto-containing silicone: 100 parts by mass of hydroxyl silicone oil (molecular weight is about 1000), 3 parts by mass of 3-mercaptopropylmethyldiethoxysilane, 2 parts by mass of tetramethylammonium hydroxide and 0.5 part by mass of deionized water are added into a reactor provided with a reflux condenser tube and a stirrer, and nitrogen is introduced for protection in the whole reaction process. Heating and stirring to 75 ℃, reacting for 10 minutes, then heating to 95 ℃, reacting for 5 hours, heating to 150 ℃, removing reflux condensation, reacting for 1 hour, transferring into a rotary evaporator, and carrying out rotary evaporation at 120 ℃ for 3 hours to obtain the organic silicon containing sulfydryl.

(2) Preparing the mercapto-containing organic silicon modified styrene-acrylic emulsion: adding 3 parts by mass of polyoxyethylene octyl phenol ether-10, 2 parts by mass of sodium dodecyl sulfate and 130 parts by mass of deionized water into a three-neck flask, and stirring at room temperature until the mixture is dissolved to obtain an emulsion. And uniformly mixing 60 parts by mass of ethyl acrylate, 40 parts by mass of propyl methacrylate, 20 parts by mass of styrene, 3 parts by mass of methacrylic acid and 12 parts by mass of mercapto-containing organosilicon in a beaker, dropwise adding the mixture into the emulsion, and dispersing the mixture at a high speed for 0.5 hour to obtain the styrene-acrylic emulsion.

4 parts by mass of potassium persulfate was dissolved in 50 parts by mass of deionized water to obtain an initiator diluted solution. 0.6 part by mass of disodium hydrogenphosphate dodecahydrate was dissolved in 60 parts by mass of deionized water to obtain a buffer diluted solution. Adding 1/3 mass of styrene-acrylic emulsion into a three-neck flask with a condensing reflux and a stirring rod, adding 2/5 of the initiator diluted solution, adding the buffer diluted solution, stirring and heating to 75 ℃ for reaction for 1 hour.

And uniformly dropwise adding the rest styrene-acrylic emulsion and the initiator diluted solution for about 2 hours, reacting for 30 minutes, and enabling the emulsion to generate a blue light phenomenon in the process. And finally, adjusting the pH to 6-8 with ammonia water, stopping the reaction, and filtering with 200-mesh filter cloth to obtain the sulfydryl-containing organic silicon modified styrene-acrylic emulsion.

(3) Coating of the mercapto-containing organosilicon styrene-acrylic emulsion: and (3) coating the obtained styrene-acrylic coating on the surface of a clean glass sheet, and drying the glass sheet at 40 ℃ for 6 hours.

The results of the stability test of the styrene-acrylic emulsion obtained in this example are shown in Table 1.

The results of the performance tests of the styrene-acrylic emulsion coating film obtained in this example are shown in Table 2.

Example 5

(1) Preparation of mercapto-containing silicone: 100 parts by mass of hydroxyl silicone oil (molecular weight is about 5000), 3 parts by mass of 3-mercaptopropylmethyldiethoxysilane, 2 parts by mass of tetramethylammonium hydroxide and 0.5 part by mass of deionized water are added into a reactor provided with a reflux condenser tube and a stirrer, and nitrogen is introduced for protection in the whole reaction process. Heating and stirring to 75 ℃, reacting for 10 minutes, then heating to 95 ℃, reacting for 5 hours, heating to 150 ℃, removing reflux condensation, reacting for 30 minutes, transferring into a rotary evaporator, and carrying out rotary evaporation at 120 ℃ for 3 hours to obtain the organic silicon containing sulfydryl.

(2) Preparing the mercapto-containing organic silicon modified styrene-acrylic emulsion: adding 3 parts by mass of polyoxyethylene octyl phenol ether-10, 1 part by mass of sodium dodecyl sulfate and 140 parts by mass of deionized water into a three-neck flask, and stirring at room temperature until the mixture is dissolved to obtain an emulsion. And uniformly mixing 70 parts by mass of lauryl acrylate, 30 parts by mass of butyl methacrylate, 10 parts by mass of styrene, 1 part by mass of acrylic acid and 20 parts by mass of mercapto-containing organic silicon in a beaker, dropwise adding the mixture into the emulsion, and dispersing the mixture at a high speed for 0.5 hour to obtain the styrene-acrylic emulsion.

1 part by mass of potassium persulfate was dissolved in 50 parts by mass of deionized water to obtain an initiator diluted solution. 0.6 part by mass of disodium hydrogenphosphate dodecahydrate was dissolved in 60 parts by mass of deionized water to obtain a buffer diluted solution. Adding 1/3 mass of styrene-acrylic emulsion into a three-neck flask with a condensing reflux and a stirring rod, adding 2/5 of the initiator diluted solution, adding the buffer diluted solution, stirring and heating to 75 ℃ for reaction for 1 hour.

And uniformly dropwise adding the rest styrene-acrylic emulsion and the initiator diluted solution for about 2 hours, reacting for 30 minutes, and enabling the emulsion to generate a blue light phenomenon in the process. And finally, adjusting the pH to 6-8 with ammonia water, stopping the reaction, and filtering with 200-mesh filter cloth to obtain the sulfydryl-containing organic silicon modified styrene-acrylic emulsion.

(3) Coating of the mercapto-containing organosilicon styrene-acrylic emulsion: and (3) coating the obtained styrene-acrylic coating on the surface of a clean glass sheet, and drying the glass sheet at 50 ℃ for 6 hours.

The results of the stability test of the styrene-acrylic emulsion obtained in this example are shown in Table 1.

The results of the performance tests of the styrene-acrylic emulsion coating film obtained in this example are shown in Table 2.

Example 6

(1) Preparation of mercapto-containing silicone: 100 parts by mass of hydroxyl silicone oil (molecular weight is about 10000), 4 parts by mass of 3-mercaptopropyl-methyldimethoxysilane, 2 parts by mass of tetramethyl-ammonium hydroxide and 0.5 part by mass of deionized water are added into a reactor provided with a reflux condenser tube and a stirrer, and nitrogen is introduced for protection in the whole reaction process. Heating and stirring to 80 ℃, reacting for 10 minutes, then heating to 100 ℃, reacting for 5 hours, heating to 150 ℃, removing reflux condensation, reacting for 30 minutes, transferring into a rotary evaporator, and carrying out rotary evaporation at 120 ℃ for 3 hours to obtain the organic silicon containing sulfydryl.

(2) Preparing the mercapto-containing organic silicon modified styrene-acrylic emulsion: 4 parts by mass of polyoxyethylene octyl phenol ether-10, 2 parts by mass of sodium dodecyl sulfate and 100 parts by mass of deionized water are added into a three-neck flask, and stirred at room temperature until the components are dissolved, so that an emulsion is obtained. And uniformly mixing 60 parts by mass of hexyl acrylate, 40 parts by mass of amyl methacrylate, 5 parts by mass of styrene, 2 parts by mass of methacrylic acid and 15 parts by mass of mercapto-containing organic silicon in a beaker, dropwise adding the mixture into the emulsion, and dispersing the mixture at a high speed for 0.5 hour to obtain the styrene-acrylic emulsion.

5 parts by mass of potassium persulfate was dissolved in 80 parts by mass of deionized water to obtain an initiator diluted solution. 0.8 part by mass of disodium hydrogenphosphate dodecahydrate was dissolved in 30 parts by mass of deionized water to obtain a buffer diluted solution. Adding 1/3 mass of styrene-acrylic emulsion into a three-neck flask with a condensing reflux and a stirring rod, adding 1/5 of the initiator diluted solution, adding the buffer diluted solution, stirring and heating to 75 ℃ for reaction for 1 hour.

And uniformly dropwise adding the rest styrene-acrylic emulsion and the initiator diluted solution for about 2 hours, and reacting for 1 hour, wherein the emulsion generates blue light in the process. And finally, adjusting the pH to 7 with ammonia water, stopping the reaction, and filtering with 200-mesh filter cloth to obtain the sulfydryl-containing organic silicon modified styrene-acrylic emulsion.

(3) Coating of the mercapto-containing organosilicon styrene-acrylic emulsion: and (3) coating the obtained styrene-acrylic coating on the surface of a clean glass sheet, and drying the glass sheet at 40 ℃ for 6 hours.

The results of the stability test of the styrene-acrylic emulsion obtained in this example are shown in Table 1.

The results of the performance tests of the styrene-acrylic emulsion coating film obtained in this example are shown in Table 2.

Example 7

(1) Preparation of mercapto-containing silicone: 100 parts by mass of hydroxyl silicone oil (molecular weight is about 850), 3 parts by mass of 3-mercaptopropyl-methyldimethoxysilane, 2 parts by mass of tetramethyl ammonium hydroxide and 0.5 part by mass of deionized water are added into a reactor provided with a reflux condenser tube and a stirrer, and nitrogen is introduced for protection in the whole reaction process. Heating and stirring to 80 ℃, reacting for 10 minutes, then heating to 100 ℃, reacting for 5 hours, heating to 150 ℃, removing reflux condensation, reacting for 30 minutes, transferring into a rotary evaporator, and carrying out rotary evaporation at 120 ℃ for 3 hours to obtain the organic silicon containing sulfydryl.

(2) Preparing the mercapto-containing organic silicon modified styrene-acrylic emulsion: adding 3 parts by mass of polyoxyethylene octyl phenol ether-10, 2 parts by mass of sodium dodecyl sulfate and 110 parts by mass of deionized water into a three-neck flask, and stirring at room temperature until the mixture is dissolved to obtain an emulsion. And uniformly mixing 60 parts by mass of amyl acrylate, 40 parts by mass of ethyl methacrylate, 10 parts by mass of styrene, 2 parts by mass of acrylic acid and 25 parts by mass of mercapto-containing organic silicon in a beaker, dropwise adding the mixture into the emulsion, and dispersing the mixture at a high speed for 0.5 hour to obtain the styrene-acrylic emulsion.

4 parts by mass of potassium persulfate was dissolved in 40 parts by mass of deionized water to obtain an initiator diluted solution. 1 part by mass of disodium hydrogen phosphate dodecahydrate was dissolved in 60 parts by mass of deionized water to obtain a buffer diluted solution. Adding 1/3 mass of styrene-acrylic emulsion into a three-neck flask with a condensing reflux and a stirring rod, adding 1/5 of the initiator diluted solution, adding the buffer diluted solution, stirring and heating to 75 ℃ for reaction for 1 hour.

And uniformly dropwise adding the rest styrene-acrylic emulsion and the initiator diluted solution for about 2 hours, reacting for 30 minutes, and enabling the emulsion to generate a blue light phenomenon in the process. And finally, adjusting the pH to 7 with ammonia water, stopping the reaction, and filtering with 200-mesh filter cloth to obtain the sulfydryl-containing organic silicon modified styrene-acrylic emulsion.

(3) Coating of the mercapto-containing organosilicon styrene-acrylic emulsion: and (3) coating the obtained styrene-acrylic coating on the surface of a clean glass sheet, and drying the glass sheet at the temperature of 35 ℃ for 8 hours.

The results of the stability test of the styrene-acrylic emulsion obtained in this example are shown in Table 1.

The results of the performance tests of the styrene-acrylic emulsion coating film obtained in this example are shown in Table 2.

TABLE 1 stability test results for mercapto-containing organosilicon modified styrene-acrylic emulsions

	Solid content%	Appearance of the emulsion	Centrifugal stability	Stability of calcium ion
					Example 1	36.1	Blue light	Stabilization	Stabilization
Example 2	39.8	Blue light	Stabilization	Stabilization
					Example 3	34.6	Blue light	Stabilization	Stabilization
Example 4	37.4	Blue light	Stabilization	Stabilization
					Example 5	35.9	Blue light	Stabilization	Stabilization
Example 6	42.3	Blue light	Stabilization	Stabilization
					Example 7	41.2	Blue light	Little delamination	Stabilization

TABLE 2 film coating performance test results of mercapto-containing organosilicon modified styrene-acrylic emulsion

	Adhesion force	Hardness of pencil	Water contact angle °	Water absorption%	Elongation%	Stress MPa
							Example 1	Stage 2	3B	73.4	5.4	517.11	2.18
Example 2	Stage 2	B	78.9	4.7	558.40	3.02
							Example 3	Level 1	B	91.8	3.2	527.19	2.71
Example 4	Stage 2	B	90.8	3.1	493.89	3.12
							Example 5	Level 1	3B	92.6	2.9	593.15	2.02
Example 6	Level 1	3B	87.5	3.5	501.82	2.57
							Example 7	Level 1	2B	95.4	2.7	523.35	2.41

The above embodiments are preferred embodiments of the present invention, but the present invention is not limited to the above embodiments, and any other changes, modifications, substitutions, combinations, and simplifications which do not depart from the spirit and principle of the present invention should be construed as equivalents thereof, and all such changes, modifications, substitutions, combinations, and simplifications are intended to be included in the scope of the present invention.