阅读说明：本技术 一种抗菌抗病毒皮革及其制备方法和应用 (Antibacterial and antiviral leather and preparation method and application thereof ) 是由 陈广川 于红光 尹珊珊 于 2020-05-27 设计创作，主要内容包括：本发明提供一种抗菌抗病毒皮革及其制备方法和应用。所述抗菌抗病毒皮革包括基布层和设置在所述基布层上的皮革面层,所述皮革面层的制备原料包括有机硅改性的无机光触媒。本发明添加有机硅改性的无机光触媒制备得到的皮革具备优异的抗菌抗病毒性能,且弹性优越、表面柔软、手感良好,皮革的热力学稳定性优异,不会因为外界环境的变化而发生变形、龟裂等现象。(The invention provides an antibacterial and antiviral leather and a preparation method and application thereof. The antibacterial and antiviral leather comprises a base cloth layer and a leather surface layer arranged on the base cloth layer, wherein the raw material for preparing the leather surface layer comprises organic silicon modified inorganic photocatalyst. The leather prepared by adding the organic silicon modified inorganic photocatalyst has excellent antibacterial and antiviral performances, excellent elasticity, soft surface, good hand feeling and excellent thermodynamic stability, and can not deform, crack and the like due to the change of external environment.)

1. The antibacterial and antiviral leather is characterized by comprising a base cloth layer and a leather surface layer arranged on the base cloth layer, wherein the raw material for preparing the leather surface layer comprises organic silicon modified inorganic photocatalyst.

2. The antibacterial and antiviral leather according to claim 1, wherein the organosilicon modified inorganic photocatalyst is prepared from the following raw materials: metal ion doped nano photocatalyst and silane coupling agent;

preferably, the mass ratio of the metal ion doped nano photocatalyst to the silane coupling agent is (25-40) to (1-2.5);

preferably, the metal ions include any one or a combination of at least two of silver ions, copper ions, zinc ions, or erbium ions;

preferably, the nano photocatalyst comprises any one or combination of at least two of nano titanium dioxide, nano zinc oxide, nano silicon dioxide, nano bismuth tungstate or nano bismuth molybdate;

preferably, the metal ion-doped nano photocatalyst comprises any one or a combination of at least two of silver ion-doped nano titanium dioxide, silver ion-doped nano bismuth tungstate, erbium ion-doped nano titanium dioxide or erbium ion-doped nano bismuth tungstate;

preferably, the particle size of the metal ion doped nano photocatalyst is 5-50 nm;

preferably, the silane coupling agent includes any one or a combination of at least two of 3-aminopropyltriethoxysilane, glycidoxypropyltrimethoxysilane, methacryloxypropyltrimethoxysilane, mercaptopropyltrimethoxysilane, mercaptopropyltriethoxysilane, or ethylenediamine propyltriethoxysilane.

3. The antibacterial and antiviral leather according to claim 1 or 2, wherein the organosilicon modified inorganic photocatalyst is prepared by the following method:

(a) mixing metal ion doped nano photocatalyst powder with an alcohol solution, dispersing and oscillating to obtain a dispersion liquid;

(b) mixing the dispersion liquid obtained in the step (a) with a silane coupling agent for reaction to obtain organic silicon modified inorganic photocatalyst reaction liquid;

preferably, the alcohol solution of step (a) is an aqueous ethanol solution;

preferably, the mass concentration of the ethanol water solution is 60-80 wt%;

preferably, the mass ratio of the metal ion doped nano photocatalyst powder in the step (a) to the alcoholic solution is (1-2): 1;

preferably, the dispersion in the step (a) is sheared by a high-speed emulsifying machine, and the rotating speed of the shearing is 1000-2000 r/min;

preferably, the oscillation in the step (a) is performed by an ultrasonic oscillator, and the oscillation time is 20-50 min;

preferably, the temperature of the mixing reaction in the step (b) is 50-80 ℃, and the time of the mixing reaction is 2-4 h;

preferably, step (b) is followed by step (c): centrifuging the organic silicon modified inorganic photocatalyst reaction solution obtained in the step (b), collecting precipitates, cleaning and drying to obtain the organic silicon modified inorganic photocatalyst;

preferably, the washing in the step (c) is carried out by using absolute ethyl alcohol, and the washing times are 3-6 times;

preferably, the drying of step (c) is vacuum drying, and the temperature of the vacuum drying is 50-80 ℃.

4. The antibacterial and antiviral leather according to any one of claims 1 to 3, wherein the raw materials for preparing the leather surface layer further comprise a thermoplastic elastic composite resin, a foaming agent and a dispersing agent;

preferably, the thermoplastic elastic composite resin comprises any one or a combination of at least two of thermoplastic polyurethane elastomer, thermoplastic TPE or thermoplastic POE;

preferably, the foaming agent comprises azodicarbonamide and/or 4,4' oxybis-benzenesulfonylhydrazide;

preferably, the dispersant comprises any one or a combination of at least two of ethylene-based bisstearamide, stearic acid monoglyceride, oleic acid amide or barium stearate;

preferably, the leather surface layer is prepared from the following raw materials in parts by weight: 90-100 parts of thermoplastic elastic composite resin, 1-10 parts of organic silicon modified inorganic photocatalyst, 2-5 parts of foaming agent and 1-5 parts of dispersing agent.

5. The antibacterial and antiviral leather according to any one of claims 1 to 4, wherein the raw materials for preparing the leather surface layer further comprise an antioxidant and/or a coloring agent;

preferably, the antioxidant comprises any one or a combination of at least two of pentaerythritol tetrakis [ beta- (3, 5-di-tert-butyl-4-hydroxyphenyl) propionate ], tris (2, 4-di-tert-butylphenyl) phosphite or octadecyl beta- (3, 5-di-tert-butyl-4-hydroxyphenyl) propionate;

preferably, the colorant comprises a toner and/or a masterbatch;

preferably, the leather surface layer is prepared from the following raw materials in parts by weight: 90-100 parts of thermoplastic elastic composite resin, 1-10 parts of organic silicon modified inorganic photocatalyst, 2-5 parts of foaming agent, 1-5 parts of dispersing agent, 1-10 parts of coloring agent and 2-5 parts of antioxidant.

6. The antibacterial and antiviral leather according to any one of claims 1 to 5, wherein the material of the base cloth layer is non-woven fabric.

7. The method for preparing antibacterial and antiviral leather according to any one of claims 1 to 6, wherein the method for preparing antibacterial and antiviral leather comprises the following steps: and adhering the leather surface layer on the base cloth layer to obtain the antibacterial and antiviral leather.

8. The method for preparing the antibacterial and antiviral leather according to claim 7, comprising the following steps:

(1) immersing the base cloth into a dimethyl formamide solution to obtain carrier liquid base cloth; mixing thermoplastic elastic composite resin, organic silicon modified inorganic photocatalyst and a dispersing agent, and then mixing with a foaming agent for foaming to obtain a hot-melt foaming body;

(2) carrying out hot-pressing adhesion on the carrier liquid base cloth obtained in the step (1) and the hot-melt foaming body to obtain the antibacterial and antiviral leather;

preferably, the liquid carrying amount of the liquid carrying base cloth in the step (1) is 0.1-0.8 kg/m;

preferably, the mixed system in the step (1) further comprises a colorant and/or an antioxidant;

preferably, the mixing of step (1) is carried out in a sealed internal mixer;

preferably, the mixing temperature in the step (1) is 120-180 ℃, and the mixing time is 10-20 min;

preferably, the foaming temperature in the step (1) is 180-250 ℃, and the foaming pressure is 10-20 MPa;

preferably, the hot-press bonding in the step (2) is performed by using a calender;

preferably, the pressure of the hot-press bonding in the step (2) is 0.1-0.8MPa, and the temperature of the hot-press bonding is 100-200 ℃.

9. The method for preparing the antibacterial and antiviral leather according to claim 8 or 9, comprising the following steps:

(1) immersing the base cloth into a dimethylformamide solution to obtain a liquid-carrying base cloth with the liquid-carrying amount of 0.1-0.8 kg/m; mixing thermoplastic elastic composite resin, organic silicon modified inorganic photocatalyst, a dispersing agent, a coloring agent and an antioxidant in a sealed internal mixer at 180 ℃ for 10-20min, and then mixing with a foaming agent at 250 ℃ and 10-20MPa for foaming to obtain a hot-melt foaming body;

(2) and (2) carrying out hot-pressing adhesion on the carrier liquid base cloth obtained in the step (1) and the hot-melt foaming body at the temperature of 100-200 ℃ and under the pressure of 0.1-0.8MPa by adopting a calender to obtain the antibacterial and antiviral leather.

10. Use of the antibacterial and antiviral leather according to any one of claims 1 to 6 for the preparation of a sports ball;

preferably, the sports ball comprises any one of a volleyball, a soccer ball, a basketball or a football.

Technical Field

The invention belongs to the technical field of leather preparation, and particularly relates to antibacterial and antiviral leather as well as a preparation method and application thereof.

Background

With the improvement of living standard of people, more and more people like to use leather products. The leather product is durable, has high quality and is not easy to go out of date, but after long-term use, bacteria and viruses are easy to breed on the surface of the leather, and the human health is greatly threatened. The existing leather product is generally only coated with a protective layer on the surface of a leather body in the preparation process, the protective layer has certain functions of crease resistance, crack resistance, sterilization and wear resistance, but the effect is poor, and the single-layer protective layer can not effectively protect the leather, so that the leather has short service life, is not friction-resistant and is easy to mildew. And the mainstream antibacterial technology applied to antibacterial leather in the market is to prepare the antibacterial leather by sterilizing nano silver and an organic antibacterial agent, but the antibacterial leather prepared by the antibacterial agent has poor antibacterial persistence and single function and cannot simultaneously achieve consistent effects on various bacteria and viruses.

CN106148579A discloses a wet rubbing resistant antibacterial leather and a manufacturing process thereof, the wet rubbing resistant antibacterial leather is prepared by soaking a leather blank in an antibacterial solution after a fatting process, drying and then coating a layer of protective film on the surface, wherein the antibacterial solution comprises: the raw materials comprise the following components in parts by weight: 35-50 parts of honeysuckle, 20-30 parts of glabrous greenbrier rhizome, 3-8 parts of chamomile, 2-7 parts of lavender and 10-20 parts of medical alcohol; the protective film includes: the raw materials comprise the following components in parts by weight: 6-15 parts of beeswax, 25-40 parts of chloroprene rubber, 1-4 parts of rosin, 12-20 parts of ethyl acetate, 0.5-1 part of nano zinc oxide, 1-3 parts of lecithin and 0.5-2 parts of prochloraz. According to the invention, the leather is wet-rubbing resistant and antibacterial by soaking the leather blank in the antibacterial liquid and coating a layer of protective film after the greasing process, but the antibacterial leather prepared by the method has poor antibacterial durability and poor virus inactivation capability.

CN109957252A discloses an antibacterial composite leather material and a preparation method thereof. The antibacterial composite leather material comprises the following components in parts by weight: the leather material has high-efficiency bactericidal performance through the synergistic effect of the titanium dioxide and the chitosan, but the antibacterial durability is poor, the function is single, the consistent effect on various bacteria and viruses cannot be achieved simultaneously, the titanium dioxide belongs to an inorganic photocatalyst material, the compatibility with the resin and the leather fibers is poor, the bactericidal performance can be influenced, and the elasticity of the leather material can also be influenced.

Therefore, there is a need to develop a leather material for sports that has high elasticity and broad-spectrum antibacterial and antiviral properties.

Disclosure of Invention

Aiming at the defects of the prior art, the invention aims to provide antibacterial and antiviral leather and a preparation method and application thereof. The antibacterial and antiviral leather has excellent antibacterial and antiviral properties, is excellent in elasticity, soft in surface and good in hand feeling, and cannot deform, crack and the like due to the change of the external environment.

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

in a first aspect, the invention provides an antibacterial and antiviral leather, which comprises a base cloth layer and a leather surface layer arranged on the base cloth layer, wherein the raw material for preparing the leather surface layer comprises an organic silicon modified inorganic photocatalyst.

In the invention, the inorganic photocatalyst modified by organic silicon is added in the raw materials for preparing the leather surface layer, so that the leather has broad-spectrum long-acting antibacterial and antiviral performance, bacteria, mould and other microorganisms attached to the surface of the leather are difficult to propagate and kill, and the high-efficiency inactivation of viruses is realized. The reason why the organic silicon is added to carry out the modification treatment on the inorganic photocatalyst on the photocatalyst material is as follows: firstly, utilize organic silicon modified inorganic photocatalyst, improved the activity of metal ion in inorganic photocatalyst, effectively improved inorganic photocatalyst's antibiotic antiviral performance, secondly the modification of organic silicon has improved the compatibility of inorganic photocatalyst material and the mixed thing of leather material, make photocatalyst even and effectively fix to the leather material in, improve the absorption rate of photocatalyst to visible light greatly, avoid inorganic photocatalyst not good and the not high problem of the absorption efficiency of visible light that leads to in the leather material dispersibility.

Preferably, the raw materials for preparing the organic silicon modified inorganic photocatalyst comprise: metal ion doped nanometer photocatalyst and silane coupling agent.

In the invention, the metal ion doped nano photocatalyst is modified by using the silane coupling agent, and the better modification effect of the silane coupling agent is caused by that one end of the silane coupling agent is oleophylic nonpolar alkyl, the other end of the silane coupling agent is hydrophilic polar oxygen-containing group, and the surface of the inorganic photocatalyst is provided with a large amount of hydrophilic polar hydroxyl; the hydrophilic oxygen-containing group at one end of the silane coupling agent and the hydroxyl on the surface of the inorganic photocatalyst are dehydrated to generate a covalent bond, and the surface of the inorganic photocatalyst is surrounded by the oleophylic alkyl at the other end of the silane coupling agent, so that the dissociation of metal ions in the inorganic photocatalyst material is effectively inhibited, and the antibacterial and antiviral performances of the inorganic photocatalyst material are improved.

Preferably, the mass ratio of the metal ion doped nano photocatalyst to the silane coupling agent is (25-40): 1-2.5.

The "25 to 40" may be, for example, 25, 26, 28, 30, 32, 34, 36, 38, 40, or the like.

The "1 to 2.5" may be, for example, 1, 1.2, 1.4, 1.6, 1.8, 2, 2.2, 2.4, 2.5, or the like.

Preferably, the metal ions include any one of silver ions, copper ions, zinc ions, or erbium ions, or a combination of at least two thereof.

Preferably, the nano photocatalyst comprises any one or combination of at least two of nano titanium dioxide, nano zinc oxide, nano silicon dioxide, nano bismuth tungstate or nano bismuth molybdate.

Preferably, the metal ion-doped nano photocatalyst comprises any one or a combination of at least two of silver ion-doped nano titanium dioxide, silver ion-doped nano bismuth tungstate, erbium ion-doped nano titanium dioxide or erbium ion-doped nano bismuth tungstate.

Preferably, the particle size of the metal ion-doped nano-photocatalyst is 5-50nm, and may be, for example, 5nm, 10nm, 15nm, 20nm, 25nm, 30nm, 35nm, 40nm, 45nm, 50nm, etc. If the particle size is too large, the photocatalytic activity of the nano photocatalyst is reduced, and the antibacterial and antiviral abilities are obviously reduced.

Preferably, the silane coupling agent includes any one or a combination of at least two of 3-aminopropyltriethoxysilane, glycidoxypropyltrimethoxysilane, methacryloxypropyltrimethoxysilane, mercaptopropyltrimethoxysilane, mercaptopropyltriethoxysilane, or ethylenediamine propyltriethoxysilane.

Preferably, the organic silicon modified inorganic photocatalyst is prepared by the following method:

(a) mixing metal ion doped nano photocatalyst powder with an alcohol solution, dispersing and oscillating to obtain a dispersion liquid;

(b) mixing the dispersion liquid obtained in the step (a) with a silane coupling agent for reaction to obtain organic silicon modified inorganic photocatalyst reaction liquid.

Preferably, the alcohol solution of step (a) is an aqueous ethanol solution.

Preferably, the ethanol aqueous solution has a mass concentration of 60 to 80 wt%, and may be, for example, 60 wt%, 62 wt%, 64 wt%, 66 wt%, 68 wt%, 70 wt%, 72 wt%, 74 wt%, 76 wt%, 78 wt%, 80 wt%, or the like.

Preferably, the mass ratio of the metal ion-doped nano photocatalyst powder in the step (a) to the alcoholic solution is (1-2):1, and may be, for example, 1:1, 12:1, 1.4:1, 1.6:1, 1.8:1, 2:1, and the like.

Preferably, the dispersion in step (a) is sheared by a high-speed emulsifying machine, and the shearing rotating speed is 1000-2000r/min, such as 1000r/min, 1200r/min, 1400r/min, 1600r/min, 1800r/min, 2000r/min, etc.

Preferably, the shaking in step (a) is performed by using an ultrasonic shaker, and the shaking time is 20-50min, such as 20min, 25min, 30min, 35min, 40min, 45min, 50min, and the like.

Preferably, the temperature of the mixing reaction in step (b) is 50-80 ℃, for example, 50 ℃, 55 ℃, 60 ℃, 65 ℃, 70 ℃, 75 ℃, 80 ℃ and the like, and the time of the mixing reaction is 2-4h, for example, 2h, 2.2h, 2.4h, 2.6h, 2.8h, 3h, 3.2h, 3.4h, 3.6h, 3.8h, 4h and the like.

Preferably, step (b) is followed by step (c): centrifuging the organic silicon modified inorganic photocatalyst reaction liquid obtained in the step (b), collecting the precipitate, cleaning and drying to obtain the organic silicon modified inorganic photocatalyst.

Preferably, the washing in step (c) is performed with absolute ethanol, and the number of washing is 3-6, and may be, for example, 3, 4, 5, 6, etc.

Preferably, the drying in step (c) is vacuum drying, and the temperature of the vacuum drying is 50-80 ℃, for example, 50 ℃, 55 ℃, 60 ℃, 65 ℃, 70 ℃, 75 ℃, 80 ℃ and the like.

Preferably, the organic silicon modified inorganic photocatalyst is prepared by the following method:

(a) mixing metal ion doped nano photocatalyst powder with an alcohol solution, shearing and dispersing at the rotating speed of 1000-2000r/min by using a high-speed emulsifying machine, and oscillating for 20-50min by using an ultrasonic oscillator to obtain a dispersion solution;

(b) mixing the dispersion liquid obtained in the step (a) with a silane coupling agent, and reacting for 2-4h at 50-80 ℃ to obtain organic silicon modified inorganic photocatalyst reaction liquid;

(c) centrifuging the organic silicon modified inorganic photocatalyst reaction liquid obtained in the step (b), collecting precipitates, cleaning for 3-6 times by using absolute ethyl alcohol, and then carrying out vacuum drying at 50-80 ℃ to obtain the organic silicon modified inorganic photocatalyst.

Preferably, the raw materials for preparing the leather surface layer also comprise thermoplastic elastic composite resin, a foaming agent and a dispersing agent.

Preferably, the thermoplastic elastomer composite resin comprises any one of thermoplastic polyurethane elastomer, thermoplastic TPE or thermoplastic POE or a combination of at least two of the thermoplastic polyurethane elastomer, the thermoplastic TPE and the thermoplastic POE.

Preferably, the blowing agent comprises azodicarbonamide and/or 4,4' oxybis-benzenesulfonylhydrazide.

Preferably, the dispersant comprises any one of ethylene bis stearamide, stearic acid monoglyceride, oleic acid amide or barium stearate or a combination of at least two thereof.

Preferably, the leather surface layer is prepared from the following raw materials in parts by weight: 90-100 parts of thermoplastic elastic composite resin, 1-10 parts of organic silicon modified inorganic photocatalyst, 2-5 parts of foaming agent and 1-5 parts of dispersing agent.

In the present invention, the content of the thermoplastic elastic composite resin is 90 to 100 parts, and may be, for example, 90 parts, 91 parts, 92 parts, 93 parts, 94 parts, 95 parts, 96 parts, 97 parts, 98 parts, 99 parts, 100 parts, or the like.

In the present invention, the content of the organic silicon-modified inorganic photocatalyst is 1 to 10 parts, and may be, for example, 1 part, 2 parts, 3 parts, 4 parts, 5 parts, 6 parts, 7 parts, 8 parts, 9 parts, 10 parts, or the like.

In the present invention, the content of the blowing agent is 2 to 5 parts, and may be, for example, 2 parts, 2.5 parts, 3 parts, 3.5 parts, 4 parts, 4.5 parts, 5 parts, or the like.

In the present invention, the content of the dispersant is 1 to 5 parts, and may be, for example, 1 part, 1.5 parts, 2 parts, 2.5 parts, 3 parts, 3.5 parts, 4 parts, 4.5 parts, 5 parts, or the like.

Preferably, the raw materials for preparing the leather surface layer also comprise an antioxidant and/or a coloring agent.

Preferably, the antioxidant comprises any one of or a combination of at least two of pentaerythritol tetrakis [ beta- (3, 5-di-tert-butyl-4-hydroxyphenyl) propionate (i.e., antioxidant 1010), tris (2, 4-di-tert-butylphenyl) phosphite (i.e., antioxidant 168), or octadecyl beta- (3, 5-di-tert-butyl-4-hydroxyphenyl) propionate (i.e., antioxidant 1076).

Preferably, the colorant comprises a toner and/or a masterbatch.

Preferably, the leather surface layer is prepared from the following raw materials in parts by weight: 90-100 parts of thermoplastic elastic composite resin, 1-10 parts of organic silicon modified inorganic photocatalyst, 2-5 parts of foaming agent, 1-5 parts of dispersing agent, 1-10 parts of coloring agent and 2-5 parts of antioxidant.

In the present invention, the content of the colorant is 1 to 10 parts, and may be, for example, 1 part, 2 parts, 3 parts, 4 parts, 5 parts, 6 parts, 7 parts, 8 parts, 9 parts, 10 parts, or the like.

In the present invention, the content of the antioxidant is 2 to 5 parts, and may be, for example, 2 parts, 2.5 parts, 3 parts, 3.5 parts, 4 parts, 4.5 parts, 5 parts, or the like.

Preferably, the base cloth layer is made of non-woven fabric.

In a second aspect, the present invention provides a method for preparing the antibacterial and antiviral leather according to the first aspect, wherein the method for preparing the antibacterial and antiviral leather comprises: and adhering the leather surface layer on the base cloth layer to obtain the antibacterial and antiviral leather.

Preferably, the preparation method of the antibacterial and antiviral leather comprises the following steps:

(1) immersing the base cloth into a dimethyl formamide solution to obtain carrier liquid base cloth; mixing thermoplastic elastic composite resin, organic silicon modified inorganic photocatalyst and a dispersing agent, and then mixing with a foaming agent for foaming to obtain a hot-melt foaming body;

(2) and (2) carrying out hot-pressing adhesion on the carrier liquid base cloth obtained in the step (1) and the hot-melt foaming body to obtain the antibacterial and antiviral leather.

In the invention, the organic silicon modified inorganic photocatalyst can be crosslinked with various organic and inorganic components in the raw materials in the mixing and hot-pressing processes, so that the dispersibility of the raw materials in banburying is improved, and meanwhile, the crosslinking structure formed in the mixing and hot-pressing processes further improves the thermodynamic stability of the leather, so that the leather cannot deform, crack and the like due to the change of the external environment.

Preferably, the liquid carrying amount of the liquid carrying base cloth in the step (1) is 0.1 to 0.8kg/m, and may be, for example, 0.1kg/m, 0.2kg/m, 0.3kg/m, 0.4kg/m, 0.5kg/m, 0.6kg/m, 0.7kg/m, 0.8kg/m, or the like.

Preferably, the mixed system in the step (1) further comprises a colorant and/or an antioxidant.

Preferably, the mixing in step (1) is carried out in a sealed internal mixer.

Preferably, the temperature for the mixing in step (1) is 120-180 ℃, for example 120 ℃, 130 ℃, 140 ℃, 150 ℃, 160 ℃, 170 ℃, 180 ℃ and the like, and the mixing time is 10-20min, for example 10min, 12min, 14min, 16min, 18min, 20min and the like.

Preferably, the foaming temperature in the step (1) is 180-250 ℃, and the foaming pressure is 10-20 MPa;

preferably, the hot-press bonding in step (2) is performed by using a calender.

Preferably, the pressure of the hot-press bonding in step (2) is 0.1-0.8MPa, such as 0.1MPa, 0.2MPa, 0.3MPa, 0.4MPa, 0.5MPa, 0.6MPa, 0.7MPa, 0.8MPa, etc., and the temperature of the hot-press bonding is 100-200 ℃, such as 100 ℃, 120 ℃, 140 ℃, 160 ℃, 180 ℃, 200 ℃, etc.

Preferably, the preparation method of the antibacterial and antiviral leather comprises the following steps:

(1) immersing the base cloth into a dimethylformamide solution to obtain a liquid-carrying base cloth with the liquid-carrying amount of 0.1-0.8 kg/m; mixing thermoplastic elastic composite resin, organic silicon modified inorganic photocatalyst, a dispersing agent, a coloring agent and an antioxidant in a sealed internal mixer at 180 ℃ for 10-20min, and then mixing with a foaming agent at 250 ℃ and 10-20MPa for foaming to obtain a hot-melt foaming body;

(2) and (2) carrying out hot-pressing adhesion on the carrier liquid base cloth obtained in the step (1) and the hot-melt foaming body at the temperature of 100-200 ℃ and under the pressure of 0.1-0.8MPa by adopting a calender to obtain the antibacterial and antiviral leather.

In a third aspect, the present invention provides the use of an antibacterial and antiviral leather according to the first aspect in the manufacture of a sports ball.

Preferably, the sports ball comprises any one of a volleyball, a soccer ball, a basketball or a football.

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

(1) the leather has good antibacterial and antiviral performances, the antibacterial rate to bacteria such as large intestine, staphylococcus aureus and the like is more than 99%, the antiviral activity rate to viruses such as H1N1, H3N2 and the like is more than 99%, the mildew-proof grade is 0, no stimulation is caused to skin, and the antibacterial and antiviral effects are very good and lasting;

(2) the antibacterial and antiviral leather has the folding fastness at normal temperature of 85000-;

(3) the organic silicon modified inorganic photocatalyst can be crosslinked with various organic and inorganic components in the raw materials in the mixing and hot-pressing processes, so that the dispersibility of the raw materials is improved, and meanwhile, the crosslinking structure formed in the mixing and hot-pressing processes further improves the thermodynamic stability of the leather, so that the leather cannot deform, crack and the like due to the change of the external environment.

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.

The sources of the components in the following examples are as follows: silver ion-doped nano titanium dioxide (manufacturer: Hangzhou Zhi Ti purification science and technology Limited, model VK-T07), silver ion-doped nano bismuth tungstate (self-made, reference: preparation characterization of doped bismuth tungstate and research on degraded dye wastewater, prepared by a hydrothermal method), erbium ion-doped nano bismuth tungstate (self-made, reference: preparation characterization of doped bismuth tungstate and research on degraded dye wastewater, prepared by a hydrothermal method), thermoplastic polyurethane elastomer (manufacturer: Shandongwowei, model 60A-72D), thermoplastic TPE (manufacturer: DuPont, model 202-8), non-woven fabrics (manufacturer: Wenzhou Wanjing non-woven fabrics Limited, model spunlaced non-woven fabrics), coloring agent (manufacturer: Pasteur, model L-arginine).

Preparation example 1

The preparation example provides an organic silicon modified inorganic photocatalyst, which is prepared by the following method:

(a) mixing 60 parts of silver ion doped nano titanium dioxide with 60 parts of ethanol water solution with the mass concentration of 70 wt%, shearing by adopting a high-speed emulsifying machine at the speed of 1200r/min to uniformly disperse the solution, and oscillating for 40min by adopting an ultrasonic oscillator to obtain a dispersion liquid;

(b) mixing the dispersion liquid obtained in the step (a) with 3 parts of 3-aminopropyltriethoxysilane, and reacting for 3 hours at 60 ℃ to obtain organic silicon modified inorganic photocatalyst reaction liquid;

(c) centrifuging the organic silicon modified inorganic photocatalyst reaction liquid obtained in the step (b), collecting precipitates, cleaning for 3 times by adopting absolute ethyl alcohol, and carrying out vacuum drying at the temperature of 60 ℃ to obtain the organic silicon modified inorganic photocatalyst.

Preparation example 2

The preparation example provides an organic silicon modified inorganic photocatalyst, which is prepared by the following method:

(a) mixing 70 parts of silver ion-doped nano bismuth tungstate with 80 parts of ethanol aqueous solution with the mass concentration of 60 wt%, shearing by a high-speed emulsifying machine at the speed of 1000r/min to uniformly disperse the solution, and oscillating for 50min by an ultrasonic oscillator to obtain a dispersion liquid;

(b) mixing the dispersion liquid obtained in the step (a) with 4 parts of glycidol-glycidoxy-propyl-trimethoxysilane, and reacting for 3 hours at 70 ℃ to obtain organic silicon modified inorganic photocatalyst reaction liquid;

(c) centrifuging the organic silicon modified inorganic photocatalyst reaction liquid obtained in the step (b), collecting precipitates, washing for 4 times by adopting absolute ethyl alcohol, and carrying out vacuum drying at 70 ℃ to obtain the organic silicon modified inorganic photocatalyst.

Preparation example 3

The preparation example provides an organic silicon modified inorganic photocatalyst, which is prepared by the following method:

(a) mixing 50 parts of erbium ion-doped nano bismuth tungstate with 60 parts of ethanol aqueous solution with the mass concentration of 80 wt%, shearing by adopting a high-speed emulsifying machine at the speed of 1500r/min to uniformly disperse the solution, and oscillating for 20min by adopting an ultrasonic oscillator to obtain a dispersion liquid;

(b) mixing the dispersion liquid obtained in the step (a) with 2 parts of methacryloxypropyltrimethoxysilane, and reacting for 4 hours at 50 ℃ to obtain organic silicon modified inorganic photocatalyst reaction liquid;

(c) centrifuging the organic silicon modified inorganic photocatalyst reaction liquid obtained in the step (b), collecting precipitates, washing for 5 times by adopting absolute ethyl alcohol, and carrying out vacuum drying at the temperature of 80 ℃ to obtain the organic silicon modified inorganic photocatalyst.

Preparation example 4

This preparation example provides an organic silicon modified inorganic photocatalyst, which is different from preparation example 1 only in that nano titanium dioxide doped with silver ions is replaced by nano titanium dioxide (without silver ion doping), and the contents of other components and the preparation method are the same as those of preparation example 1.

Preparation example 5

The preparation example provides an organic silicon modified inorganic photocatalyst, which is different from the preparation example 1 only in that the content of the silver ion doped nano titanium dioxide is increased to 62 parts, the content of 3-aminopropyl triethoxysilane is reduced to 1 part, and the content of other components and the preparation method are the same as the preparation example 1.

Preparation example 6

The preparation example provides an organic silicon modified inorganic photocatalyst, which is different from the preparation example 1 only in that the content of the silver ion doped nano titanium dioxide is increased to 53 parts, the content of 3-aminopropyl triethoxysilane is reduced to 10 parts, and the content of other components and the preparation method are the same as the preparation example 1.

Preparation example 7

The preparation example provides an organic silicon modified inorganic photocatalyst, and the difference from the preparation example 1 is that after the dispersion in the step (a), the ultrasonic oscillator is not used for oscillation, and the obtained dispersion liquid is directly subjected to the reaction in the step (b).

Preparation example 8

The preparation example provides an organic silicon modified inorganic photocatalyst, and the difference from the preparation example 1 is that after the mixing in the step (a), a high-speed emulsifying machine is not used for shearing, and the oscillation of an ultrasonic oscillator is prolonged to 1 hour.