阅读说明：本技术 一种抗菌抗病毒组合物、抗菌抗病毒涂层和容器 (Antibacterial and antiviral composition, antibacterial and antiviral coating and container ) 是由 陈广川 于红光 尹珊珊 于 2020-07-13 设计创作，主要内容包括：本发明涉及一种抗菌抗病毒组合物、抗菌抗病毒涂层和容器,所述抗菌抗病毒组合物包括如下组分：不饱和化合物或不饱和树脂、光引发剂和含氟硅烷偶联剂改性的无机抗菌抗病毒剂。本发明提供的抗菌抗病毒组合物能够形成具有优异的抗菌抗病毒性能的涂层,对皮肤无刺激,抗菌抗病毒剂的利用率高,且效果持久,同时涂层具有较高的硬度、耐磨性能和热力学稳定性能,可以将其涂覆在水杯等容器的外表面,得到具有上述性能的抗菌抗病毒容器。(The invention relates to an antibacterial and antiviral composition, an antibacterial and antiviral coating and a container, wherein the antibacterial and antiviral composition comprises the following components: unsaturated compound or unsaturated resin, photoinitiator and inorganic antibacterial and antiviral agent modified by fluorine-containing silane coupling agent. The antibacterial and antiviral composition provided by the invention can form a coating with excellent antibacterial and antiviral properties, has no stimulation to skin, high utilization rate of antibacterial and antiviral agents and lasting effect, has higher hardness, wear resistance and thermodynamic stability, and can be coated on the outer surface of containers such as water cups and the like to obtain the antibacterial and antiviral containers with the properties.)

1. An antibacterial and antiviral composition, which is characterized by comprising the following components: unsaturated compound or unsaturated resin, photoinitiator and inorganic antibacterial and antiviral agent modified by fluorine-containing silane coupling agent.

2. The antibacterial and antiviral composition according to claim 1, wherein the inorganic antibacterial and antiviral agent comprises any one or at least two of tetrabutyl titanate, ethyl orthosilicate, zinc nitrate hexahydrate, ammonium tungstate, stannic chloride, bismuth tungstate or bismuth nitrate in combination;

preferably, the fluorine-containing silane coupling agent comprises any one or at least two of tridecafluorooctyltrimethoxysilane, heptadecafluorodecyltrimethoxysilane, trifluoropropylmethyldimethoxysilane, 1H,2H, 2H-perfluorodecyltriethoxysilane or dodecafluoroheptylpropyltrimethoxysilane.

3. The antibacterial and antiviral composition according to claim 1 or 2, wherein the preparation method of the inorganic antibacterial and antiviral agent modified by the fluorine-containing silane coupling agent comprises: mixing the hydrolysate of the inorganic antibacterial and antiviral agent with a fluorine-containing silane coupling agent to obtain the inorganic antibacterial and antiviral agent modified by the fluorine-containing silane coupling agent;

preferably, the preparation method of the inorganic antibacterial and antiviral agent modified by the fluorine-containing silane coupling agent comprises the following steps:

(1) hydrolyzing the inorganic antibacterial antiviral agent;

(2) mixing the hydrolysate obtained in the step (1) with a fluorine-containing silane coupling agent to obtain the inorganic antibacterial antiviral agent modified by the fluorine-containing silane coupling agent;

preferably, the ratio of the fluorine-containing silane coupling agent to the inorganic antibacterial and antiviral agent is (0.02-1): 1;

preferably, in step (2), stirring is performed after the mixing;

preferably, the stirring time is 1-3 h;

preferably, step (2) further comprises: adjusting the pH of a reaction system to 6-7 by using an acid reagent, removing a solvent, and drying to obtain the inorganic antibacterial antiviral agent modified by the fluorine-containing silane coupling agent;

preferably, the method of removing the solvent comprises rotary evaporation;

preferably, the temperature of the drying is 40-80 ℃;

preferably, the drying time is 12-48 h;

preferably, the step (1) specifically comprises the following steps:

(1a) mixing inorganic antibacterial antiviral agent with anhydrous ethanol, and stirring;

(1b) mixing the solution obtained in the step (1a) with ammonia water, stirring, and adjusting the pH of a reaction system to 6-7 by using an acidic reagent;

preferably, in the step (1a), the stirring time is 30-60 min;

preferably, the molar concentration of the inorganic antibacterial and antiviral agent in the solution obtained in the step (1a) is 0.14-1.67 mol/L;

preferably, in the step (1b), the mass fraction of the ammonia water is 20-40 wt%, preferably 30 wt%;

preferably, in the step (1b), the volume ratio of the solution obtained in the step (1a) to the ammonia water is 1:3-1: 6;

preferably, in the step (1b), the ammonia water is dropwise added into the solution obtained in the step (1 a);

preferably, in the step (1b), the concentration of the acidic reagent is 0.01-0.05 mol/L;

preferably, in the step (1b), the stirring time is 10-40 min;

preferably, the acidic reagent comprises any one or a combination of at least two of nitric acid, sulfuric acid, sulfurous acid, hydrochloric acid, phosphoric acid, acetic acid, or formic acid;

preferably, the preparation method of the inorganic antibacterial and antiviral agent modified by the fluorine-containing silane coupling agent specifically comprises the following steps:

(1a) mixing the inorganic antibacterial antiviral agent with absolute ethyl alcohol, and stirring for 30-60min to obtain an inorganic antibacterial antiviral agent solution with the concentration of 0.14-1.67 mol/L;

(1b) dropwise adding ammonia water with the mass fraction of 20-40 wt% into the solution obtained in the step (1a), stirring for 10-40min, and adding an acidic reagent with the concentration of 0.01-0.05mol/L to adjust the pH of the reaction system to 6-7, wherein the volume ratio of the solution obtained in the step (1a) to the ammonia water is 1:3-1: 6;

(2) and (2) mixing the product obtained in the step (1b) with a fluorine-containing silane coupling agent, stirring for 1-3h, adjusting the pH of a reaction system to 6-7 by using an acid reagent, removing the solvent, and drying at the temperature of 40-80 ℃ for 12-48h to obtain the inorganic antibacterial and antiviral agent modified by the fluorine-containing silane coupling agent.

4. The antibacterial and antiviral composition according to any of claims 1 to 3, wherein the unsaturated resin comprises urethane acrylate;

preferably, the unsaturated compound comprises 1, 6-hexanediol diacrylate and/or tripropylene glycol diacrylate.

5. The anti-bacterial and anti-viral composition according to any one of claims 1 to 4, wherein the photoinitiator comprises any one or a combination of at least two of the photoinitiators 184, 1173, 2959.

6. The antibacterial and antiviral composition according to any of claims 1 to 5, wherein the antibacterial and antiviral composition further comprises a leveling agent;

preferably, the leveling agent comprises any one or at least two of polydimethylsiloxane, polyether polyester modified organic siloxane, alkyl modified organic siloxane or polyacrylate.

7. The antibacterial and antiviral composition according to any one of claims 1 to 6, wherein the antibacterial and antiviral composition comprises the following components in parts by weight:

8. an antibacterial and antiviral coating, characterized in that it is obtained by curing the antibacterial and antiviral composition according to any one of claims 1 to 7.

9. A container having an outer surface coated with the antibacterial and antiviral coating of claim 8.

10. The container of claim 9, wherein the container comprises a cup, bowl, or dish;

preferably, the container comprises an antibacterial and antiviral water cup;

preferably, the material of the container is ceramic, stainless steel or aluminum alloy.

Technical Field

The invention relates to the technical field of antibacterial and antiviral containers, in particular to an antibacterial and antiviral composition, an antibacterial and antiviral coating and a container.

Background

The containers such as water cups and bowls are the most common drinking and eating tools in daily life. However, due to the fact that working pressure is high, life rhythm is fast, operation is complex, the frequency of cleaning and disinfecting containers by general users is relatively low, bacteria and viruses are easy to breed in the long-term use process of the containers under the condition, human health is greatly threatened, and therefore in order to protect human health and improve the human health level, a high-efficiency antibacterial and antiviral container needs to be prepared urgently.

CN107713610A discloses an antibiotic drinking cup, it includes cup and bowl cover, has two water intakes at least on the bowl cover, the water intake be provided with the screw thread lid, the cup surface have antibiotic layer, antibiotic layer is medical antibiotic material of high strength. The cup cover is provided with at least two water inlets, the water inlets are provided with threaded covers, the situation that multiple people share one water inlet to cause cross infection of viruses is prevented, and the surface of the cup body is provided with an antibacterial layer. However, the antibacterial water cup provided by the invention has poor antibacterial effect and antiviral effect, and meanwhile, the durable antibacterial effect and antiviral effect are difficult to realize.

CN103554881A discloses an antibacterial polycarbonate material for a water cup shell, which is prepared from the following raw materials in parts by weight: 500-520 parts of polycarbonate, 35-38 parts of high-density polyethylene, 30-34 parts of polyethylene terephthalate, 12-15 parts of nano titanium dioxide, 1-2 parts of nano silver oxide, 20-24 parts of polyethylene glycol, 12-14 parts of chopped glass fiber, 15201.3-1.8 parts of antioxidant, 5-9 parts of glycerol, 5-6 parts of epoxy linseed oil and 10-12 parts of assistant. The invention adds the nanometer titanium dioxide and the nanometer silver oxide, has natural antibacterial and bacteriostatic effects, and has high strength and elastic coefficient, high impact strength, wide range of use temperature, stable quality, low forming shrinkage, good dimensional stability, no odor and harmlessness to human body, and is suitable for manufacturing the shell of the water cup. However, the antibacterial filler is directly added into the cup body material, only the antibacterial filler on the surface can actually realize the real antibacterial effect, waste is caused, and the antibacterial and antiviral effects and the durability of the antibacterial and antiviral cup body material are all to be improved.

CN202009965U discloses a wear-resistant antibacterial water cup. Specifically, a wear-resistant antibacterial UV photocuring coating is coated on the surface of a common water cup so as to achieve the wear-resistant antibacterial effect. The wear-resistant antibacterial Ultraviolet (UV) curing coating is formed by mixing polyurethane acrylate, benzoin ethyl ether, dimethyl ethanolamine and nano titanium dioxide powder according to a mass ratio and irradiating by Ultraviolet (UV). The film has a thickness of 0.1 to 0.3 microns. The utility model discloses a wear-resisting antibiotic drinking cup that provides's antiviral effect is relatively poor, and antibiotic effect is not lasting.

Therefore, there is a need in the art to develop an antibacterial and antiviral coating or an antibacterial and antiviral cup with excellent and durable antibacterial and antiviral properties, and to sufficiently improve the utilization rate of the antibacterial and antiviral agents, while having excellent mechanical properties and thermodynamic properties.

Disclosure of Invention

One of the objectives of the present invention is to provide an antibacterial and antiviral composition, which can form a coating having excellent antibacterial and antiviral properties, is non-irritating to the skin, has a high utilization rate of the antibacterial and antiviral agent, and has a long-lasting effect, and at the same time, the coating has high hardness, wear resistance, and thermodynamic stability.

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

the invention provides an antibacterial and antiviral composition, which comprises the following components: unsaturated compound or unsaturated resin, photoinitiator and inorganic antibacterial and antiviral agent modified by fluorine-containing silane coupling agent.

The invention utilizes the surface migration characteristic of fluoride, uses the fluoride to modify inorganic antibacterial antiviral agents to obtain the antibacterial antiviral agents with migration, and adds the antibacterial antiviral agents into the composition, wherein the antibacterial antiviral agents with migration can migrate to the gas-liquid surface of a coating system in a photopolymerization system and are enriched on the surface. Meanwhile, the composition system has the photopolymerization characteristic, so that the migrating antibacterial and antiviral agent can be fixed on the surface of the polymer matrix of the coating material through the chemical bonding effect, the antibacterial and antiviral performance of the surface of the polymer coating is effectively improved, and the utilization efficiency of the antibacterial and antiviral agent can be improved. The antibacterial performance of the cured coating on escherichia coli and staphylococcus aureus reaches more than 99%, the antiviral activity rate on H3N2 and H1N1 influenza viruses is more than 99%, and the coating is non-toxic, non-irritant to skin and has a very good lasting effect.

In addition, the added antibacterial antiviral agent is an inorganic antibacterial antiviral agent, and the inorganic particles have higher hardness, so that the antibacterial and antiviral coating has higher surface hardness and excellent wear resistance;

in addition, the introduction of inorganic antibacterial antiviral agent in the photopolymerization system and the use of fluorine-containing silane coupling agent endow the antibacterial and antiviral coating with excellent thermodynamic stability, so that the coating does not shrink or crack along with the change of external temperature.

In the present invention, in the "unsaturated compound or unsaturated resin", the unsaturated compound means a small molecule compound having an unsaturated bond, which is not polymerized, and the unsaturated resin means a polymer having an unsaturated bond, and either of them may be contained in the composition of the present invention.

In the present invention, the modification is physical modification.

In the invention, the inorganic antibacterial and antiviral agent modified by the fluorine-containing silane coupling agent comprises a hydrolysate of the inorganic antibacterial and antiviral agent and the fluorine-containing silane coupling agent, and the hydrolysate and the fluorine-containing silane coupling agent are connected by hydrogen bonds.

Preferably, the inorganic antibacterial and antiviral agent comprises any one or at least two of tetrabutyl titanate, ethyl orthosilicate, zinc nitrate hexahydrate, ammonium tungstate, tin chloride, bismuth tungstate or bismuth nitrate.

The invention preferably selects several specific inorganic antibacterial antiviral agents, has excellent photocatalyst effect compared with other types of antibacterial antiviral agents, and has antibacterial function under the conditions of light or no light.

Preferably, the fluorine-containing silane coupling agent comprises any one or at least two of tridecafluorooctyltrimethoxysilane, heptadecafluorodecyltrimethoxysilane, trifluoropropylmethyldimethoxysilane, 1H,2H, 2H-perfluorodecyltriethoxysilane or dodecafluoroheptylpropyltrimethoxysilane.

Preferably, the preparation method of the inorganic antibacterial and antiviral agent modified by the fluorine-containing silane coupling agent comprises the following steps: and mixing the hydrolysate of the inorganic antibacterial and antiviral agent with a fluorine-containing silane coupling agent to obtain the inorganic antibacterial and antiviral agent modified by the fluorine-containing silane coupling agent.

Preferably, the preparation method of the inorganic antibacterial and antiviral agent modified by the fluorine-containing silane coupling agent comprises the following steps:

(1) hydrolyzing the inorganic antibacterial antiviral agent;

(2) and (2) mixing the hydrolysate obtained in the step (1) with a fluorine-containing silane coupling agent to obtain the inorganic antibacterial antiviral agent modified by the fluorine-containing silane coupling agent.

Preferably, the ratio of the amount of the fluorine-containing silane coupling agent to the inorganic antibacterial/antiviral agent is (0.02 to 1: 1), for example, 0.1:1, 0.2:1, 0.3:1, 0.4:1, 0.5:1, 0.6:1, 0.7:1, 0.8:1, 0.9:1, or the like.

Further, the ratio of the two reaction raw materials is optimized, so that the antibacterial and antiviral effects, the hardness, the wear resistance and the thermodynamic stability of the coating are further improved. Too much or too little fluorine-containing silane coupling agent can reduce the hardness and thermodynamic stability, and too much fluorine-containing silane coupling agent can also cause the prepared antibacterial and antiviral composition to have higher viscosity, difficult coating and poorer coating leveling property.

Preferably, in step (2), stirring is performed after the mixing.

Preferably, the stirring time is 1-3h, such as 1.2h, 1.4h, 1.6h, 1.8h, 2h, 2.2h, 2.4h, 2.6h, 2.8h, and the like.

Preferably, step (2) further comprises: and (3) adjusting the pH of the reaction system to 6-7 by using an acid reagent, removing the solvent, and drying to obtain the inorganic antibacterial and antiviral agent modified by the fluorine-containing silane coupling agent.

Preferably, the method of removing the solvent comprises rotary evaporation.

Preferably, the drying temperature is 40-80 deg.C, such as 45 deg.C, 50 deg.C, 55 deg.C, 60 deg.C, 65 deg.C, 70 deg.C, 75 deg.C, etc.

Preferably, the drying time is 12-48h, such as 14h, 16h, 18h, 20h, 22h, 24h, 26h, 28h, 30h, 32h, 34h, 36h, 38h, 40h, 42h, 44h, 46h, and the like.

Preferably, the step (1) specifically comprises the following steps:

(1a) mixing inorganic antibacterial antiviral agent with anhydrous ethanol, and stirring;

(1b) and (2) mixing the solution obtained in the step (1a) with ammonia water, stirring, and adjusting the pH of the reaction system to 6-7 by using an acidic reagent.

Preferably, in step (1a), the stirring time is 30-60min, such as 32min, 34min, 36min, 38min, 40min, 42min, 44min, 46min, 48min, 50min, 52min, 54min, 56min, 58min, etc.

Preferably, the molar concentration of the inorganic antibacterial and antiviral agent in the solution obtained in step (1a) is 0.14-1.67 mol/L, such as 0.2mol/L, 0.4mol/L, 0.6mol/L, 0.8mol/L, 1mol/L, 1.2mol/L, 1.4mol/L, 1.6mol/L, etc.

Preferably, in step (1b), the mass fraction of the aqueous ammonia is 20 to 40 wt%, such as 22 wt%, 24 wt%, 26 wt%, 28 wt%, 30 wt%, 32 wt%, 34 wt%, 36 wt%, 38 wt%, etc., preferably 30 wt%.

Preferably, in step (1b), the volume ratio of the solution obtained in step (1a) to ammonia is 1:3 to 1:6, such as 1:3.2, 1:3.4, 1:3.6, 1:3.8, 1:4, 1:4.2, 1:4.4, 1:4.6, 1:4.8, 1:5, 1:5.2, 1:5.4, 1:5.6, 1:5.8, etc.

Preferably, in step (1b), the aqueous ammonia is added dropwise to the solution obtained in step (1 a).

Preferably, in step (1b), the concentration of the acidic reagent is 0.01-0.05mol/L, such as 0.02mol/L, 0.03mol/L, 0.04mol/L, and the like.

Preferably, in step (1b), the stirring time is 10-40min, such as 15min, 20min, 25min, 30min, 35min, etc.

Preferably, the acidic reagent comprises any one or a combination of at least two of nitric acid, sulfuric acid, sulfurous acid, hydrochloric acid, phosphoric acid, acetic acid, or formic acid.

Preferably, the preparation method of the inorganic antibacterial and antiviral agent modified by the fluorine-containing silane coupling agent specifically comprises the following steps:

(1a) mixing the inorganic antibacterial antiviral agent with absolute ethyl alcohol, and stirring for 30-60min to obtain an inorganic antibacterial antiviral agent solution with the concentration of 0.14-1.67 mol/L;

(1b) dropwise adding ammonia water with the mass fraction of 20-40 wt% into the solution obtained in the step (1a), stirring for 10-40min, and adding an acidic reagent with the concentration of 0.01-0.05mol/L to adjust the pH of the reaction system to 6-7, wherein the volume ratio of the solution obtained in the step (1a) to the ammonia water is 1:3-1: 6;

(2) and (2) mixing the product obtained in the step (1b) with a fluorine-containing silane coupling agent, stirring for 1-3h, adjusting the pH of a reaction system to 6-7 by using an acid reagent, removing the solvent, and drying at the temperature of 40-80 ℃ for 12-48h to obtain the inorganic antibacterial and antiviral agent modified by the fluorine-containing silane coupling agent.

Preferably, the unsaturated resin comprises urethane acrylate.

Preferably, the unsaturated compound comprises 1, 6-hexanediol diacrylate and/or tripropylene glycol diacrylate.

Preferably, the photoinitiator comprises any one or a combination of at least two of photoinitiator 184, photoinitiator 1173, or photoinitiator 2959.

Preferably, the antibacterial and antiviral composition further comprises a leveling agent.

Preferably, the leveling agent comprises any one or at least two of polydimethylsiloxane, polyether polyester modified organic siloxane, alkyl modified organic siloxane or polyacrylate.

Preferably, the antibacterial and antiviral composition comprises the following components in parts by weight:

the content of the unsaturated compound or unsaturated resin is 80 to 90 parts by weight, for example, 81 parts by weight, 82 parts by weight, 83 parts by weight, 84 parts by weight, 85 parts by weight, 86 parts by weight, 87 parts by weight, 88 parts by weight, 89 parts by weight, and the like.

The photoinitiator may be present in an amount of 1 to 5 parts by weight, for example, 1.5 parts by weight, 2 parts by weight, 2.5 parts by weight, 3 parts by weight, 3.5 parts by weight, 4 parts by weight, 4.5 parts by weight, and the like.

The content of the fluorine-containing silane coupling agent modified inorganic antibacterial and antiviral agent is 2-10 parts by weight, such as 3 parts by weight, 4 parts by weight, 5 parts by weight, 6 parts by weight, 7 parts by weight, 8 parts by weight, 9 parts by weight and the like.

The content of the leveling agent is 1 to 5 parts by weight, for example, 1.5 parts by weight, 2 parts by weight, 2.5 parts by weight, 3 parts by weight, 3.5 parts by weight, 4 parts by weight, 4.5 parts by weight, or the like.

In the present invention, the preparation method of the antibacterial and antiviral composition is simple mixing of the components, and a person skilled in the art may change the specific mixing manner according to the actual situation, which is not specifically limited in the present invention.

The second object of the present invention is to provide an antibacterial and antiviral coating obtained by curing the antibacterial and antiviral composition according to the first object.

The antibacterial and antiviral coating provided by the invention is a product obtained after the antibacterial and antiviral composition is subjected to photocuring, and the antibacterial and antiviral performance, hardness, wear resistance and thermodynamic stability of the antibacterial and antiviral coating are as described above.

The third object of the present invention is to provide a container having an outer surface coated with the second objective antibacterial and antiviral coating.

Preferably, the container comprises a cup, bowl or dish.

Preferably, the container comprises an antibacterial and antiviral water cup.

Preferably, the material of the container is ceramic, stainless steel or aluminum alloy.

Compared with the prior art, the invention has the following beneficial effects:

the antibacterial and antiviral coating provided by the invention has the antibacterial performance of more than 99% on escherichia coli and staphylococcus aureus, the antiviral activity rate of more than 99% on H3N2 and H1N1 influenza viruses, and the antibacterial and antiviral coating is nontoxic, has no stimulation to skin and has a very good lasting effect. Meanwhile, the coating has high surface hardness and high thermodynamic stability of wear resistance, and the coating cannot shrink or crack along with the change of external temperature.

The hardness of the antibacterial and antiviral coating is 7H-8H, the thermal deformation temperature is 260-300 ℃, and even 280-300 ℃.

Detailed Description

The technical solution of the present invention is further explained by the following embodiments. It should be understood by those skilled in the art that the examples are only for the understanding of the present invention and should not be construed as the specific limitations of the present invention.

Synthesis example 1

The synthetic example provides an inorganic antibacterial antiviral agent modified by a fluorine-containing silane coupling agent, and the preparation method comprises the following steps:

s1: dissolving 0.03mol of tetrabutyl titanate in 50mL of absolute ethyl alcohol, and magnetically stirring for 40min at room temperature until the tetrabutyl titanate is completely dissolved;

s2: dissolving and mixing 30 wt% of ammonia water and the solution prepared from S1 according to the volume ratio of 1:4 (dropwise adding the ammonia water into the solution prepared from S1), magnetically stirring for 30min, and adding 0.03mol/L nitric acid to adjust the pH to 6-7;

s3: adding 0.005mol of tridecafluorooctyl trimethoxysilane into the solution prepared by S2, magnetically stirring for reaction for 2 hours, and adjusting the pH value to 6-7 by using nitric acid;

s4: and (3) rotationally evaporating the S3 solution, and drying for 30h in vacuum at 60 ℃ to obtain the inorganic antibacterial antiviral agent 1 modified by the fluorine-containing silane coupling agent.

Synthesis example 2

The difference from synthetic example 1 is that tetrabutyl titanate is replaced by tetraethoxysilane in the same amount as the tetrabutyl titanate to obtain the inorganic antibacterial and antiviral agent 2 modified by the fluorine-containing silane coupling agent.

Synthesis example 3

The difference from synthetic example 1 is that the inorganic antibacterial/antiviral agent 3 modified with the fluorine-containing silane coupling agent was obtained by replacing tetrabutyl titanate with zinc nitrate hexahydrate in an equivalent amount.

Synthesis example 4

The difference from synthetic example 1 is that the inorganic antibacterial/antiviral agent 4 modified with the fluorine-containing silane coupling agent was obtained by replacing tetrabutyl titanate with ammonium tungstate in an equivalent amount.

Synthesis example 5

The difference from synthetic example 1 is that the inorganic antibacterial/antiviral agent 5 modified with the fluorine-containing silane coupling agent was obtained by replacing tetrabutyl titanate with tin chloride in an amount equivalent to that of the above-mentioned compound.

Synthesis example 6

The difference from synthetic example 1 is that the inorganic antibacterial/antiviral agent 6 modified with the fluorine-containing silane coupling agent was obtained by replacing tetrabutyl titanate with bismuth nitrate in an equivalent amount.

Synthesis example 7

The difference from synthetic example 1 is that the inorganic antibacterial/antiviral agent 7 modified with the fluorine-containing silane coupling agent was obtained by replacing tetrabutyl titanate with an equivalent amount of bismuth tungstate.

Synthesis example 8

The difference from synthetic example 1 is that tetrabutyl titanate was added in an amount of 0.01mol and tridecafluorooctyltrimethoxysilane was added in an amount of 0.01mol to give an inorganic antibacterial/antiviral agent 8 modified with a fluorine-containing silane coupling agent.

Synthesis example 9

The difference from synthetic example 1 is that tetrabutyl titanate is added in an amount of 0.05mol and tridecafluorooctyltrimethoxysilane is added in an amount of 0.001mol, to obtain an inorganic antibacterial/antiviral agent 9 modified with a fluorine-containing silane coupling agent.

Synthesis example 10

The difference from synthetic example 1 is that tetrabutyl titanate is added in an amount of 0.01mol and tridecafluorooctyltrimethoxysilane is added in an amount of 0.02mol, to obtain an inorganic antibacterial/antiviral agent 10 modified with a fluorine-containing silane coupling agent.

Synthesis example 11

The difference from synthetic example 1 is that tetrabutyl titanate is added in an amount of 0.06mol and tridecafluorooctyltrimethoxysilane is added in an amount of 0.001mol, to obtain an inorganic antibacterial/antiviral agent 11 modified with a fluorine-containing silane coupling agent.

Synthesis example 12

The synthetic example provides an inorganic antibacterial antiviral agent modified by a fluorine-containing silane coupling agent, and the preparation method comprises the following steps:

s1: dissolving 0.02mol of tetrabutyl titanate in 30mL of absolute ethyl alcohol, and magnetically stirring for 30min at room temperature until the tetrabutyl titanate is completely dissolved;

s2: dissolving and mixing 20 wt% ammonia water and the solution prepared from S1 according to the volume ratio of 1:3 (ammonia water is dropwise added into the solution prepared from S1), magnetically stirring for 10min, and adding 0.01mol/L sulfuric acid to adjust the pH value to 6-7;

s3: adding 0.005mol of heptadecafluorodecyltrimethoxysilane into the solution prepared by S2, magnetically stirring for reaction 1, and adjusting the pH value to 6-7 by using sulfuric acid;

s4: and (3) rotationally evaporating the S3 solution 40, and drying for 48 hours in vacuum to obtain the inorganic antibacterial and antiviral agent 12 modified by the fluorine-containing silane coupling agent.

Synthesis example 13

The synthetic example provides an inorganic antibacterial antiviral agent modified by a fluorine-containing silane coupling agent, and the preparation method comprises the following steps:

s1: dissolving 0.03mol of tetrabutyl titanate in 70mL of absolute ethyl alcohol, and magnetically stirring for 60min at room temperature until the tetrabutyl titanate is completely dissolved;

s2: dissolving and mixing 40 wt% of ammonia water and the solution prepared from S1 according to the volume ratio of 1:6 (dropwise adding ammonia water into the solution prepared from S1), magnetically stirring for 40min, and adding 0.05mol/L hydrochloric acid to adjust the pH to 6-7;

s3: adding 0.006mol of trifluoropropylmethyldimethoxysilane into the solution prepared by S2, magnetically stirring for reaction for 3 hours, and then adjusting the pH value to 6-7 by hydrochloric acid;

s4: and (3) rotationally evaporating the S3 solution, and drying for 12h in vacuum at the temperature of 80 ℃ to obtain the inorganic antibacterial antiviral agent 13 modified by the fluorine-containing silane coupling agent.

Comparative Synthesis example 1

The difference from synthetic example 1 is that the antibacterial and antiviral agent D1 was obtained by replacing tridecafluorooctyltrimethoxysilane with gamma-aminopropyltriethoxysilane in an equivalent amount.

Comparative Synthesis example 2

The difference from synthetic example 1 is that the antibacterial and antiviral agent D2 was obtained by replacing tridecafluorooctyltrimethoxysilane with poly (meth) acrylic acid fluoroalkyl ester in an equivalent amount.

Some of the material information used in the following examples is as follows:

urethane acrylate: purchased from Guangzhou Tongyi New materials science and technology Co., Ltd under the brand name YWU 2620; polydimethylsiloxane: purchased from Guangzhou Donghong chemical Co Ltd, and the brand number is PMX-50PMX-100 PMX-3;

tripropylene glycol diacrylate: purchased from Conditis chemical (Hubei) Co., Ltd., under the designation 42978-66-5);

alkyl-modified organosiloxane: purchased from Jintenglong industry Co., Ltd, Shenzhen, and having a brand name Tego Antifoam 1015;

1, 6-hexanediol diacrylate: purchased from Nantong garden chemical Co., Ltd, and having a brand number of 2082-81-7;

polyether polyester modified organosiloxane: purchased from Nanjing Tian you chemical Co., Ltd and having a brand name of A002.