阅读说明：本技术 一种具有自补偿疏水表面功能的水性高分子乳液及其制备方法 (Water-based polymer emulsion with self-compensation hydrophobic surface function and preparation method thereof ) 是由 伍燕 张银琳 刘希婧 苗成成 于 2021-07-05 设计创作，主要内容包括：本发明涉及一种具有自补偿疏水表面功能的水性高分子乳液及其制备方法,属于水性高分子制备技术领域。本发明公开了一种具有自补偿疏水表面功能的水性高分子的制备方法,在制备过程中使用的原材料易得,且制备过程仅使用少量有机溶剂不会造成生产安全问题,适合工业大规模的生产。通过本发明的制备方法得到的具有自补偿疏水表面功能的水性高分子,能适用于多数基材且施工工艺简单,适合工业化应用；另一方面,本发明提供的水性高分子成膜后具备自动补偿表面疏水物质的功能,即使在膜表面受损的情况下,也可为表面提供持久且稳定的疏水性能；当使用此水性高分子作为涂层的基体树脂,为制备耐久性超疏水、自清洁涂层和防腐涂层提供了一种简单可行的方法。(The invention relates to a water-based polymer emulsion with a self-compensating hydrophobic surface function and a preparation method thereof, belonging to the technical field of water-based polymer preparation. The invention discloses a preparation method of a water-based polymer with a self-compensation hydrophobic surface function, raw materials used in the preparation process are easy to obtain, and the preparation process only uses a small amount of organic solvent, does not cause the production safety problem, and is suitable for industrial large-scale production. The water-based polymer with the self-compensating hydrophobic surface function obtained by the preparation method can be suitable for most base materials, has a simple construction process and is suitable for industrial application; on the other hand, the water-based polymer provided by the invention has the function of automatically compensating surface hydrophobic substances after film formation, and can provide lasting and stable hydrophobic performance for the surface even if the surface of the film is damaged; when the aqueous polymer is used as the matrix resin of the coating, a simple and feasible method is provided for preparing durable super-hydrophobic, self-cleaning coatings and anticorrosive coatings.)

1. A preparation method of an aqueous polymer emulsion with a self-compensating hydrophobic surface function is characterized by comprising the following steps:

(1) preparing a polydimethylsiloxane-g-polyurethane prepolymer: mixing isophorone diisocyanate, polypropylene glycol, polycaprolactone, dimethylolpropionic acid, single-ended dihydroxy alkyl polydimethylsiloxane and 1, 4-butanediol, adding dibutyltin dilaurate as a catalyst, reacting at 85 ℃ until the theoretical NCO value in the system is reached, finishing the reaction, and cooling to normal temperature;

(2) preparing a water-based polymer: adding triethylamine to neutralize carboxyl in the polydimethylsiloxane-g-polyurethane prepolymer to obtain a high-molecular ionomer, then adding an end-capping agent and a fluorine-containing cross-linking agent, continuing to react with the ionomer, finally adding an aqueous solution containing ethylenediamine, and dispersing at the rotating speed of 600-1000 rpm to obtain the water-based high-molecular emulsion.

2. The method according to claim 1, wherein M is the molecular weight of the polypropylene glycol_n2000g/mol, M of said polycaprolactone_nM of said single-ended bishydroxyhydrocarbyl polydimethylsiloxane 2000g/mol_n＝1600g/mol。

3. The preparation method according to claim 1, wherein in the step (1), the isophorone diisocyanate is 4-7 parts, the polypropylene glycol is 0-6 parts, the polycaprolactone is 5-10 parts, the dimethylolpropionic acid is 0.3-0.8 part, the single-ended bishydroxyalkyl polydimethylsiloxane is 0.5-6 parts, the 1, 4-butanediol is 0-0.5 part, and the catalyst is 0.01-0.03 part by weight.

4. The method according to claim 1, wherein in the step (2), the blocking agent is 3-aminopropyltriethoxysilane, and the fluorine-containing crosslinking agent is 1H,1H,2H, 2H-perfluorooctyltriethoxysilane.

5. The method according to claim 1, wherein the molar ratio of triethylamine to dimethylolpropionic acid in step (1) in step (2) is 1: 1;

0.23-0.6 part of triethylamine, 0-1 part of end-capping reagent, 0-1 part of fluorine-containing cross-linking agent and 0.24-0.5 part of ethylenediamine.

6. The aqueous polymer emulsion with the self-compensating hydrophobic surface function prepared by the preparation method according to any one of claims 1 to 5.

7. The aqueous polymer emulsion according to claim 6, wherein the aqueous polymer contains 5 to 35% by mass of Si and 0 to 5% by mass of F; the organic volatile content is < 5%.

8. An aqueous coating with a self-compensating hydrophobic surface function, which is characterized in that the aqueous polymer emulsion of any one of claims 7 to 8 is used as a coating matrix resin in the aqueous coating.

9. A method for preparing the aqueous coating of claim 8, comprising the steps of:

the aqueous polymer emulsion of any one of claims 6 to 7 is used as coating matrix resin, inorganic filler or organic filler, dispersant, wetting agent and defoaming agent are respectively added into the matrix resin for mixing, and the mixture is dispersed at high speed at the rotating speed of 600 to 1000rpm to form the aqueous coating.

10. The method according to claim 9, wherein the aqueous polymer is 25 to 100 parts by weight, the inorganic filler is 6 to 30 parts by weight, the organic filler is 6 to 30 parts by weight, the dispersant is 0.1 to 1 part by weight, the wetting agent is 0.1 to 1 part by weight, and the defoaming agent is 0.05 to 1 part by weight;

the inorganic filler is barium sulfate, the organic filler is PTFE micropowder, the dispersing agent is COADIS BR3, the wetting agent is TEGO4100, and the defoaming agent is BYK 028.

Technical Field

The invention belongs to the technical field of preparation of water-based polymers, and relates to a water-based polymer emulsion with a self-compensation hydrophobic surface function and a preparation method thereof.

Background

Hydrophobic materials generally have properties such as corrosion resistance, self-cleaning, ice-over resistance, stain resistance, and bacteria resistance due to their low surface energy. It is widely applied to industrial and agricultural production and daily life of people and becomes a research hotspot of materials. The hydrophobicity of a material is mainly determined by the surface geometry and chemical composition of the material, and the degree of wetting of a solid surface by a liquid, that is, the hydrophobicity of the material surface, is usually characterized by a static contact angle. A solid surface contact angle <90 ° is a hydrophilic surface, and a contact angle >90 ° is a hydrophobic surface. While an increase in surface roughness may increase the hydrophilicity/hydrophobicity of the surface. Generally, a flexible hydrophobic membrane material is prepared by introducing a hydrophobic chain segment (such as a fluorine chain, a silicon chain, a long aliphatic chain and the like) into a high molecular chain to provide low surface energy, and further improving the hydrophobicity of the material by blending or chemically combining inorganic nanoparticles. While the hydrophobic functional monomer is usually less in the whole matrix resin, the low surface energy of the hydrophobic chain segment can spontaneously migrate from the interior of the matrix to the surface, and a layered hydrophobic coating with the hydrophobic chain segment as the surface and the matrix resin at the bottom layer is actually formed. In many cases in practical applications, loss of surface hydrophobic substances can be caused by mechanical friction, liquid drop impact, organic pollutants, illumination and the like, and surface properties such as surface adhesion, friction and wettability are finally affected, so that the hydrophobic function of the surface is lost. Obviously, these irreversible damages shorten the useful life of the hydrophobic surface material and severely limit its application in industrial fields. While crosslinking or building up the elastic nanocomposite structure coating can improve the durability of the hydrophobic coating to some extent, it does not solve the problem per se.

Therefore, the preparation of functional materials with active compensation of hydrophobic substances, which imitate the self-repairing function of some natural organisms such as lotus leaves, is beginning to attract the attention of researchers. On the basis, the preparation and application of the environment-friendly self-compensation hydrophobic surface material with low VOC and even zero VOC have more important scientific and economic significance in response to the national sustainable development strategy.

Disclosure of Invention

In view of the above, an object of the present invention is to provide an aqueous polymer emulsion with self-compensating hydrophobic surface function; the second purpose of the invention is to provide a preparation method of the water-based polymer emulsion with the self-compensating hydrophobic surface function; the invention also aims to provide a water-based coating which takes the water-based polymer emulsion with the self-compensating hydrophobic surface function as the matrix resin of the coating; the fourth purpose of the invention is to provide a preparation method of the water-based coating with the self-compensation hydrophobic surface function.

In order to achieve the purpose, the invention provides the following technical scheme:

1. a preparation method of an aqueous polymer emulsion with a self-compensating hydrophobic surface function comprises the following steps:

(1) preparing a polydimethylsiloxane-g-polyurethane prepolymer: mixing isophorone diisocyanate (IPDI), polypropylene glycol (PPG, M)_n2000g/mol), polycaprolactone (PCL, M)_n2000g/mol), dimethylolpropionic acid (DMPA), single-ended bishydroxyalkyl polydimethylsiloxane (PDMS, M)_n1600g/mol) and 1, 4-Butanediol (BDO), adding dibutyltin dilaurate (DBTDL) as a catalyst, reacting at 85 ℃ until the theoretical NCO value in the system is reached, finishing the reaction, and cooling to the normal temperature;

(2) preparing a water-based polymer: and adding Triethylamine (TEA) to neutralize carboxyl in the polydimethylsiloxane-g-polyurethane prepolymer to obtain a high-molecular ionomer, then adding an end-capping agent and a fluorine-containing cross-linking agent, continuing to react with the ionomer, finally adding an aqueous solution containing Ethylenediamine (EDA), and dispersing at the rotating speed of 600-1000 rpm to obtain the water-based high-molecular emulsion.

Preferably, M of said polypropylene glycol_n2000g/mol, M of said Polycaprolactone (PCL)_nM of said mono-terminal bishydroxyhydrocarbyl Polydimethylsiloxane (PDMS) at 2000g/mol_n＝1600g/mol。

Preferably, in the step (1), by weight, 4-7 parts of isophorone diisocyanate (IPDI), 0-6 Parts of Polypropylene Glycol (PPG), 5-10 parts of Polycaprolactone (PCL), 0.3-0.8 part of dimethylolpropionic acid (DMPA), 0.5-6 parts of single-end dihydroxy alkyl Polydimethylsiloxane (PDMS), 0-0.5 part of 1, 4-Butanediol (BDO) and 0.01-0.03 part of catalyst are used.

Preferably, in the step (2), the blocking agent is 3-Aminopropyltriethoxysilane (APTES), and the fluorine-containing crosslinking agent is 1H,1H,2H, 2H-Perfluorooctyltriethoxysilane (PFTES).

Preferably, in the step (2), the molar ratio of the Triethylamine (TEA) to the dimethylolpropionic acid (DMPA) in the step (1) is 1: 1;

0.23-0.6 part of Triethylamine (TEA), 0-1 part of end capping agent, 0-1 part of fluorine-containing cross-linking agent and 0.24-0.5 part of ethylenediamine.

2. The aqueous polymer emulsion with the self-compensating hydrophobic surface function is prepared by the preparation method.

Preferably, the mass percent of Si and F in the water-based polymer is 5-35% and 0-5%; the organic volatile content is < 5%.

3. The water-based coating with the self-compensation hydrophobic surface function takes the water-based polymer emulsion as coating matrix resin.

Preferably, the method comprises the steps of:

the aqueous polymer emulsion is used as coating matrix resin, inorganic filler or organic filler, dispersant, wetting agent and defoamer are respectively added into the matrix resin for mixing, and the mixture is dispersed at a high speed at a rotating speed of 600-1000 rpm to form the aqueous coating.

Preferably, the water-based polymer is 25-100 parts by weight, the inorganic filler is 6-30 parts by weight, the organic filler is 6-30 parts by weight, the dispersant is 0.1-1 part by weight, the wetting agent is 0.1-1 part by weight, and the defoaming agent is 0.05-1 part by weight;

the inorganic filler is barium sulfate, the organic filler is PTFE micropowder, the dispersing agent is COADIS BR3, the wetting agent is TEGO4100, and the defoaming agent is BYK 028.

The invention has the beneficial effects that:

1. the invention discloses a preparation method of a water-based polymer with a self-compensation hydrophobic surface function, raw materials used in the preparation process are easy to obtain, and the preparation process only uses a small amount of organic solvent, does not cause the production safety problem, and is suitable for industrial large-scale production. The water-based polymer with the self-compensating hydrophobic surface function obtained by the preparation method disclosed by the invention has excellent thermal stability and mechanical properties, and also has excellent adhesive force to a wide range of base materials, and a specific curing process is not required in the forming process, so that the construction process is simple, and the water-based polymer is suitable for wide industrial application; in addition, the polymer material has the function of automatically compensating surface hydrophobic substances under the condition of surface abrasion, and provides lasting and stable hydrophobic performance for the surface.

2. The water-based polymer with the self-compensating hydrophobic surface function prepared by the invention is suitable for being used as matrix resin of a water-based coating, a simple and feasible method is provided for preparing a durable super-hydrophobic and self-cleaning coating, the provided hydrophobic coating still has excellent surface hydrophobicity after the surface of the hydrophobic coating is repeatedly worn under pressure, and the surface contact angle can reach about 140 degrees.

Additional advantages, objects, and features of the invention will be set forth in part in the description which follows and in part will become apparent to those having ordinary skill in the art upon examination of the following or may be learned from practice of the invention. The objectives and other advantages of the invention may be realized and attained by the means of the instrumentalities and combinations particularly pointed out hereinafter.

Drawings

For the purposes of promoting a better understanding of the objects, aspects and advantages of the invention, reference will now be made to the following detailed description taken in conjunction with the accompanying drawings in which:

FIG. 1 is a schematic diagram of the preparation process of the aqueous polymer having the self-compensating hydrophobic surface function in example 1;

FIG. 2 shows the EDS test results of the aqueous polymer emulsion coating film with self-compensating hydrophobic surface function in example 1 after 30 times of abrasion-repair;

FIG. 3 is the contact angle change of the film material formed by coating the water-based polymer emulsion with the self-compensating hydrophobic surface function on the glass sheet in example 1 before and after abrasion-repair;

FIG. 4 is the adhesion test result of the aqueous polymer emulsion with the self-compensating hydrophobic surface function coated on different materials in example 1;

FIG. 5 is the thermal stability of the aqueous polymer film with self-compensating hydrophobic surface function of example 1;

FIG. 6 is the salt spray resistance test result of the aqueous polymer emulsion coating film with self-compensating hydrophobic surface function on the steel plate in example 1;

FIG. 7 is a graph showing the change in contact angle of the surface before and after abrasion-repair of an aqueous coating having a self-compensating hydrophobic surface function prepared in example 2 applied to a glass plate;

FIG. 8 shows the self-cleaning effect of the aqueous coating with self-compensating hydrophobic surface function prepared in example 2, wherein a, b and c are the effect before rinsing, during the falling of the droplets and after rinsing, respectively.

Detailed Description

The embodiments of the present invention are described below with reference to specific embodiments, and other advantages and effects of the present invention will be easily understood by those skilled in the art from the disclosure of the present specification. The invention is capable of other and different embodiments and of being practiced or of being carried out in various ways, and its several details are capable of modification in various respects, all without departing from the spirit and scope of the present invention. It should be noted that the drawings provided in the following embodiments are only for illustrating the basic idea of the present invention in a schematic way, and the features in the following embodiments and examples may be combined with each other without conflict.

Example 1

1. The structure schematic diagram of the prepared prepolymer and the final product is shown in figure 1, and the specific method is as follows:

(1) preparing a polydimethylsiloxane-g-polyurethane prepolymer: according to the weight parts, 5 parts of isophorone diisocyanate (IPDI), 4 parts of polypropylene glycol (PPG, 2000g/mol), 6 parts of polycaprolactone (PCL,2000g/mol), 0.7 part of dimethylolpropionic acid (DMPA), 2.25 parts of single-ended dihydroxy alkyl polydimethylsiloxane (PDMS,1600g/mol) and 0.3 part of 1, 4-Butanediol (BDO) are taken, 0.01 part of dibutyltin dilaurate (DBTDL) is added as a catalyst, the reaction is finished when the mass percent of NCO is 3.47%, and the temperature is reduced to the normal temperature to obtain a polydimethylsiloxane-g-polyurethane prepolymer;

(2) preparing a water-based polymer: adding 0.42 part of Triethylamine (TEA) (wherein the molar number of the Triethylamine (TEA) is the same as that of dimethylolpropionic acid (DMPA) in the step (1)) to neutralize carboxyl in the polydimethylsiloxane-g-polyurethane prepolymer to obtain a high-molecular ionomer, then adding 1 part of end-capping agent 3-Aminopropyltriethoxysilane (APTES) and 1 part of fluorine-containing crosslinking agent 1H,1H,2H, 2H-Perfluorooctyltriethoxysilane (PFTES), continuing to react with the neutralized ionomer for 1H, adding a mixed solution of 0.24 part of Ethylenediamine (EDA) and 35 parts of water, and dispersing at a high speed of 800rpm for 2H to form an emulsion.

The materials comprise dibutyl tin dilaurate (DBTDL), dimethylolpropionic acid (DMPA), polypropylene glycol (PPG) and Polycaprolactone (PCL) which are dehydrated under reduced pressure at 120 ℃ for 2h before use, and 1, 4-Butanediol (BDO) is dehydrated under reduced pressure at 80 ℃ for 2h before use.

2. The performance of the waterborne polymer with the self-compensating hydrophobic surface function prepared in the above way is tested:

(1) coating the water-based self-compensating hydrophobic polymer on a glass sheet, drying at room temperature until the surface is dry, and drying the excessive water at 60-100 ℃ until the weight is constant. A500 g standard weight was placed on 200# sandpaper, and the sandpaper was pulled to make the weight move one turn over the coating, which was recorded as the number of sanding times 1. The above steps are cycled through polishing the coatings 10, 30, 70 and 100 times respectively. The polished membrane material recovers the surface performance after being subjected to heat treatment for 2 hours at 40 ℃. The test film material is subjected to 30 times of abrasion-repair and the change of surface elements, and the result is shown in figure 2; the film material was tested for changes in surface contact angle before and after several wear-repairs, and the results are shown in FIG. 3. All tests show that after the coating is abraded and repaired, the surface composition of the coating can be smoothly restored to an unworn initial state, the proportion of surface silicon element is restored in the coating restoration process, the proportion of surface polar component oxygen element is reduced, the restored surface has more excellent hydrophobic property, and the static contact angle (WCA) is increased to 111 degrees from 106 degrees.

(2) The aqueous self-compensating hydrophobic polymer is coated on glass, wood board, tinplate and other substrates respectively, and the adhesion performance of the coating film to the substrate is tested by using a 3M test adhesive tape with reference to GB/T9286-1998, and the result is shown in FIG. 4. The results demonstrate that the coating film hardly comes off under 3M tape, demonstrating excellent adhesion to glass, wood and tinplate.

(4) The thermal stability of the aqueous polymer film having a self-compensating hydrophobic surface function of example 1 was tested, and the results are shown in fig. 5. The initial degradation temperature of the polymer film is 286.9 ℃, the degradation is carried out in two stages, the degradation peak temperature of the first stage is 315.1 ℃, and the degradation peak temperature of the second stage is 401.7 ℃, which indicates that the polymer film has better thermal stability.

(5) The water-based self-compensating hydrophobic polymer is coated on the surface of the steel plate in any one of a paving mode, a coating mode, a soaking mode or a spraying mode, before the steel plate is used, 5% NaOH solution and 5% HCl solution are respectively used for washing away surface grease, and then a large amount of deionized water is used for washing and cleaning the surface. After the surface of the polymer on the surface of the steel plate is dried, drying the excessive water of the coating film at the temperature of 60-100 ℃ to constant weight, and controlling the thickness of the dry film to be 80 +/-5 mu m. The salt spray resistance test of the coating is carried out according to the standard GB1771-79, the corrosion medium is 5 percent NaCl aqueous solution, the pH value is 6.5-7.2, the ambient temperature is 35 ℃, and the spraying is continuously uninterrupted in the test time. The test result is shown in fig. 6, after the coating is respectively subjected to salt spray for 100h and 200h, rust bubbles and rust spreading are not found at the initial scratch, and the salt spray resistance of the polymer film is good, which indicates that the material has excellent corrosion resistance. .

Example 2

1. The aqueous polymer with the self-compensating hydrophobic surface function prepared in example 1 is used as a coating matrix resin to prepare an aqueous coating with the self-compensating hydrophobic surface function, and the specific method is as follows:

(1) weighing 50 parts of the water-based polymer with the self-compensating hydrophobic surface function prepared in the example 1, sequentially adding 0.13 part of dispersing agent (COADIS BR3) and 0.3 part of wetting agent (TEGO4100) into a beaker, and starting a shearing machine to perform high-speed dispersion at 600 rpm;

(2) sequentially and slowly adding 13 parts of barium sulfate and 13 parts of PTFE micro powder, and maintaining shearing for 0.5 h;

(3) and continuously adding 0.1 part of defoaming agent (BYK028), dispersing for 0.5h at a high speed, and standing for defoaming to obtain the water-based paint with the self-compensation hydrophobic surface function.

2. The performance test of the water-based coating prepared above was carried out:

the water-based coating with the self-compensating hydrophobic surface function prepared in the example 2 is coated on a glass sheet, dried to be surface dry at room temperature, and then dried to be constant weight at 60-100 ℃. And (3) placing a 500g standard weight on No. 200 sand paper, dragging the sand paper to enable the weight to move on the coating for one circle, recording the polishing times as 1 time, and repeating the steps to polish the coatings for 10, 30, 70 and 100 times respectively. The polished membrane material is subjected to heat treatment at 40 ℃ for 10min and then the surface performance of the membrane material is recovered. The film material was tested for changes in surface contact angle before and after several wear-repairs, and the results are shown in fig. 7. The water-based coating prepared by the water-based polymer emulsion with the self-compensating hydrophobic surface function has good wear resistance.

Self-cleaning action of the coating: the surface of the prepared water-based coating in example 2 is pressed with a certain amount of dust as shown in fig. 8(a), the dust on the surface is washed by water drops, the dust is easily taken away in the rolling process of the water drops as shown in fig. 8(b), and the final washing effect of the coating is shown in fig. 8 (c). The water-based coating prepared by the water-based polymer with the self-compensation hydrophobic surface function has good self-cleaning performance.

Example 3

1. The preparation method of the water-based polymer emulsion with the self-compensating hydrophobic surface function comprises the following steps:

(1) preparing a polydimethylsiloxane-g-polyurethane prepolymer: taking 4 parts of isophorone diisocyanate (IPDI), 10 parts of polycaprolactone (PCL,2000g/mol), 0.5 part of dimethylolpropionic acid (DMPA), 0.5 part of single-ended dihydroxy alkyl polydimethylsiloxane (PDMS,1600g/mol) and 0.2 part of 1, 4-Butanediol (BDO), adding 0.03 part of dibutyltin dilaurate (DBTDL) as a catalyst, reacting at 85 ℃ until the theoretical NCO value in the system is reached, finishing the reaction, and cooling to normal temperature to obtain a polydimethylsiloxane-g-polyurethane prepolymer;

(2) preparing a water-based polymer: adding 0.38 part of Triethylamine (TEA) (wherein the molar number of the Triethylamine (TEA) is the same as that of dimethylolpropionic acid (DMPA) in the step (1)) to neutralize carboxyl in the polydimethylsiloxane-g-polyurethane prepolymer to obtain a high-molecular ionomer, then adding 0.1 part of end-capping agent 3-Aminopropyltriethoxysilane (APTES), continuing to react with the ionomer after neutralization for 1h, adding a mixed solution of 0.31 part of Ethylenediamine (EDA) and 35 parts of water, and dispersing at a high speed of 600rpm for 2h to form an emulsion.

The materials comprise dibutyl tin dilaurate (DBTDL), dimethylolpropionic acid (DMPA), polypropylene glycol (PPG) and Polycaprolactone (PCL) which are dehydrated under reduced pressure at 120 ℃ for 2h before use, and 1, 4-Butanediol (BDO) is dehydrated under reduced pressure at 80 ℃ for 2h before use.

Example 4

1. The preparation method of the water-based polymer emulsion with the self-compensating hydrophobic surface function comprises the following steps:

(1) preparing a polydimethylsiloxane-g-polyurethane prepolymer: according to the weight parts, taking 7 parts of isophorone diisocyanate (IPDI), 3 Parts of Polypropylene Glycol (PPG), 7 parts of polycaprolactone (PCL,2000g/mol), 0.8 part of dimethylolpropionic acid (DMPA), 5 parts of single-ended dihydroxy alkyl polydimethylsiloxane (PDMS,1600g/mol) and 0.5 part of 1, 4-Butanediol (BDO), adding 0.02 part of dibutyltin dilaurate (DBTDL) as a catalyst, reacting at 85 ℃ until the theoretical NCO value in the system is reached, finishing the reaction, and reducing the temperature to normal temperature to obtain a polydimethylsiloxane-g-polyurethane prepolymer;

(2) preparing an aqueous polymer emulsion: adding 0.6 part of Triethylamine (TEA) (wherein the molar number of the Triethylamine (TEA) is the same as that of dimethylolpropionic acid (DMPA) in the step (1)) to neutralize carboxyl in the polydimethylsiloxane-g-polyurethane prepolymer to obtain a polymer ionomer, then adding 0.5 part of end-capping agent 3-Aminopropyltriethoxysilane (APTES), continuing to react with the neutralized ionomer for 1 hour by 0.5 part of fluorine-containing cross-linking agent (PFTES), adding a mixed solution of 0.42 part of Ethylenediamine (EDA) and 35 parts of water, and dispersing at a high speed for 1 hour at the rotating speed of 1000rpm to form an emulsion.

The materials comprise dibutyl tin dilaurate (DBTDL), dimethylolpropionic acid (DMPA), polypropylene glycol (PPG) and Polycaprolactone (PCL) which are subjected to dehydration treatment at 120 ℃ under reduced pressure for 2h before use, and 1, 4-Butanediol (BDO) is dehydrated at 80 ℃ under reduced pressure for 2h before use.

The aqueous polymer emulsions having a self-compensating hydrophobic surface function prepared in examples 3 and 4 were also tested to have the same self-compensating hydrophobic surface effect as in example 1.

Example 5

The aqueous polymer emulsion with the self-compensating hydrophobic surface function prepared in example 3 was used to prepare an aqueous coating with the self-compensating hydrophobic surface function according to the following method:

25 parts of the water-based polymer emulsion with the self-compensating hydrophobic surface function prepared in the example 1 is used as a coating matrix resin, 6 parts of inorganic filler (barium sulfate), 6 parts of organic filler (PTFE micropowder), 0.1 part of dispersing agent (COADIS BR3), 0.1 part of wetting agent (TEGO4100) and 0.05 part of defoaming agent (BYK028) are respectively added into the matrix resin for mixing, and the mixture is dispersed at a high speed at the rotating speed of 600rpm to form the water-based paint.

In conclusion, the invention discloses a preparation method of a water-based polymer with a self-compensation hydrophobic surface function, raw materials used in the preparation process are easy to obtain, the preparation process does not depend on large-scale precise instruments, and the preparation process only uses a small amount of organic solvent, does not cause production safety problems, and is suitable for industrial large-scale production. The water-based polymer with the self-compensating hydrophobic surface function prepared by the preparation method has excellent thermal stability and mechanical property, and the PDMS chain segment cannot be debonded from the polyurethane matrix to influence the mechanical property of the polyurethane matrix; the surface hydrophobic material automatic compensation device also has the function of automatically compensating surface hydrophobic materials and provides lasting and stable surface performance for the surface. In addition, the water-based polymer with the self-compensating hydrophobic surface function, which is prepared by the invention, is used as the coating matrix resin of the water-based coating with the self-compensating hydrophobic surface function, the surface hydrophobicity of the water-based coating can be improved, the coating still has excellent surface hydrophobicity after the surface is repeatedly pressurized and worn, the surface contact angle can reach about 140 degrees, and the self-cleaning performance is good. The water-based polymer with the self-compensating hydrophobic surface function, which is prepared by the invention, is used as the matrix resin of the anticorrosive coating, can resist salt spray for 200h, and has an excellent anticorrosive effect.

Finally, the above embodiments are only intended to illustrate the technical solutions of the present invention and not to limit the present invention, and although the present invention has been described in detail with reference to the preferred embodiments, it will be understood by those skilled in the art that modifications or equivalent substitutions may be made on the technical solutions of the present invention without departing from the spirit and scope of the technical solutions, and all of them should be covered by the claims of the present invention.