阅读说明：本技术 一种水溶性阻燃超双疏涂料、制备方法及涂层 (Water-soluble flame-retardant super-amphiphobic coating, preparation method and coating ) 是由 王玉忠 王芳 宋飞 孙仁义 李春波 于 2021-10-08 设计创作，主要内容包括：本发明公开了一种水溶性阻燃超双疏涂料、制备方法及涂层,按重量百分比计,包括：微纳粒子0.1～5％、阻燃剂0.1～5％、双组份低表面能物质0.4～20％,余量为溶剂；双组份低表面能物质包括A组分和B组分,A组分为含氟或含碳的表面活性剂,B组分为含氟低表面能物质；其中A组分至少占双组份低表面能物质质量的10％；本发明提供的水溶性阻燃超双疏涂料将微纳粒子、阻燃剂和双组分低表面能物质相结合,通过多组分的协同效应实现了材料的高阻燃和表面的超双疏性；得到的涂料可以用于木质建筑保护、生活家居及特种防护服等多种基材,可解决当前阻燃涂料有效成分易流失、耐候性差的问题,满足对易燃材料阻燃防火、表面抗水拒油和绿色环保长效耐候的要求。(The invention discloses a water-soluble flame-retardant super-amphiphobic coating, a preparation method and a coating, which comprise the following components in percentage by weight: 0.1-5% of micro-nano particles, 0.1-5% of flame retardant, 0.4-20% of double-component low-surface-energy substance and the balance of solvent; the two-component low surface energy substance comprises a component A and a component B, wherein the component A is a fluorine-containing or carbon-containing surfactant, and the component B is a fluorine-containing low surface energy substance; wherein the component A at least accounts for 10 percent of the mass of the two-component low surface energy substance; the water-soluble flame-retardant super-amphiphobic coating provided by the invention combines micro-nano particles, a flame retardant and a bi-component low-surface-energy substance, and realizes high flame retardance and super-amphiphobic property of the surface of the material through a multi-component synergistic effect; the obtained coating can be used for various base materials such as wood building protection, living homes, special protective clothing and the like, can solve the problems of easy loss of effective components and poor weather resistance of the conventional flame-retardant coating, and meets the requirements of flame retardance, fire resistance, water and oil resistance of the surface, environmental protection, long-term weather resistance of the flammable material.)

1. The water-soluble flame-retardant super-amphiphobic coating is characterized by comprising the following components in percentage by weight:

0.1-5% of micro-nano particles, 0.1-5% of flame retardant, 0.4-20% of double-component low-surface-energy substance and the balance of solvent;

the two-component low surface energy substance comprises a component A and a component B, wherein the component A is a fluorine-containing or carbon-containing surfactant, and the component B is a fluorine-containing low surface energy substance; wherein the component A at least accounts for 10 percent of the mass of the two-component low surface energy substance.

2. The water-soluble flame-retardant super-amphiphobic coating as claimed in claim 1, wherein the micro-nano particles are one or a mixture of two or more of silicon dioxide, zinc oxide, titanium dioxide, aluminum oxide, aluminum nitride, magnesium oxide, magnesium hydroxide, cobalt hydroxide, zirconium oxide, silver sulfide, calcium carbonate, silver particles, graphene, carbon nanotubes, polyurea formaldehyde, polystyrene, polyacrylamide, polytetrafluoroethylene, polyvinylidene fluoride and polymethyl methacrylate in any proportion.

3. The water-soluble flame-retardant super-amphiphobic coating of claim 1, wherein, the flame retardant is one or a mixture of two or more of ammonium polyphosphate, ethanolamine-modified ammonium polyphosphate, ethylenediamine-modified ammonium polyphosphate, propylenediamine-modified ammonium polyphosphate, piperazine-modified ammonium polyphosphate, ammonium polyphosphate derivatives, polyphosphate, ammonium phosphate salts, melamine polyphosphate, phosphate esters, hypophosphite, melamine cyanurate, melamine phosphate, melamine polyphosphate, antimony trioxide, dithiophosphate, neopentyl dithiophosphate, tetraethyl orthosilicate, alkali metal ions, alkaline earth metal ions, transition metal ions, sodium metasilicate pentahydrate, polysilicic acid, polydimethylsiloxane, aluminum tripolyphosphate, tricresyl phosphate, triphenyl phosphite, dimethyl methylphosphonate and stannous zincate in any proportion.

4. The water-soluble flame-retardant super-amphiphobic coating as claimed in claim 1, wherein the component A is one or a mixture of two or more of acrylate emulsion, styrene-acrylic emulsion, silicone-acrylic emulsion, polyvinyl acetate acrylate emulsion, polyurethane dispersion, ethylene acrylate emulsion, polysorbate, sodium dodecyl sulfate, cetyl trimethyl ammonium bromide, fluorinated acrylic copolymer, fluorinated polyurethane copolymer, fluorine-containing nonionic surfactant, fluorine-containing anionic surfactant and fluorine-containing cationic surfactant in any proportion.

5. The water-soluble flame-retardant super-amphiphobic coating as claimed in claim 1, wherein the component B is one or a mixture of two or more of fluorooctyldimethylchlorosilane, perfluorooctanoyl chloride, perfluoroheptanoic acid, perfluorooctanoic acid, polyperfluoroethylpropylene, perfluoroalkoxy, a perfluorinated cyclic polymer, p-trifluoromethoxyaniline and a derivative thereof, 4- (4-trifluoromethoxyphenylazo) phenol and a derivative thereof, a fluorinated long-chain alcohol, a fluorinated long-chain amine and a fluorine-containing silane coupling agent in any proportion; the fluorine-containing silane coupling agent has the following linear structural formula:

(CH₃O)₃Si(CH₂)₂(CF₂)nCF₃、

(CH₃CH₂O)₃Si(CH₂)₂(CF₂)nCF₃or

Cl₃Si(CH₂)₂(CF₂)nCF₃，

Wherein n is more than or equal to 1.

6. The preparation method of the water-soluble flame-retardant super-amphiphobic coating as claimed in any one of claims 1 to 5, which is characterized by comprising the following steps:

step 1: dispersing the micro-nano particles, the flame retardant and the component A low-surface-energy substance in a solvent, and stirring for full reaction to obtain a dispersion liquid;

step 2: and (3) dispersing the component B low-surface-energy substance in the dispersion liquid obtained in the step (1), and continuously stirring and fully reacting to obtain the required water-soluble flame-retardant super-amphiphobic coating.

7. The preparation method according to claim 6, wherein the reaction time in the step 1 is 0.5 to 96 hours.

8. The preparation method according to claim 6, wherein the reaction time in the step 2 is 0.5 to 96 hours.

9. The coating prepared by the coating obtained by the preparation method according to claims 6-7, wherein the coating is coated on a substrate to obtain the required coating.

10. The coating of claim 9, wherein the coating process is one of a roll-bake, spray-coating, brush-coating, or dip-coating process; the base material is one of a high polymer material base material, an inorganic non-metal material base material and a metal material base material.

Technical Field

The invention relates to the technical field of coatings and preparation methods, in particular to a water-soluble flame-retardant super-amphiphobic coating, a preparation method and a coating.

Background

Fire disasters threaten public safety and social development, and the French Paris Binery Hospital suffers from intense fire in 2019 in the 4 th month, and the wooden roof truss is completely burnt, so that the whole building is seriously damaged. Except for historical buildings and precious cultural relics, materials commonly used in daily life, such as bamboo building materials, cotton, hemp, silk, fiber textiles and the like, are easy to spontaneously combust due to low ignition temperature and low oxygen index. Once it catches fire, it is very easy to cause the spread of fire behavior to enlarge, thus increase the danger of fire. Therefore, it is important to flame-retardant these flammable materials. At present, various methods are available for flame retardant modification of flammable materials, wherein flame retardant coatings are used for flame retardant treatment of flammable material surfaces, or coatings are constructed on material surfaces, which is an effective way to reduce flammability of materials. The method has simple operation, does not change the intrinsic performance of the base material and the like, and is widely applied. However, most flame retardant coatings have hydrophilic structures, poor water resistance and oil stain resistance, and have the defects of poor compatibility with substrates, easy migration and precipitation from the substrates under high temperature and high humidity conditions, and the like. And the material after the surface treatment of the flame-retardant coating has the problems of flame retardant loss and flame retardant effect reduction after being soaked or washed by water, so that the use of the material is limited.

The super-amphiphobic surface refers to a surface with the static contact angles of water and oil on the surface of more than 150 degrees and the rolling angle of less than 10 degrees, can resist water, oil and wetting by various organic solvents, and the like, and can be widely applied to oil stain resistance and corrosion resistance treatment of various materials such as textiles, wood, metal, plastics and the like. The prepared super-amphiphobic surface generally has a rough structure and lower surface free energy. For example, fluorosilane and n-butyl cyanoacrylate are dispersed in dichloropentafluoropropane solvent, and the obtained solution is coated on the surface of a material by a dip coating or spray coating method, so that a multiple concave rough structure can be constructed to obtain a super-amphiphobic surface. For example, the super-amphiphobic hydrophobic surface can be obtained by chemically modifying the surface of a substrate such as fiber, fabric and the like with isocyanate and then placing the substrate in a solution of a low surface energy substance such as hydroxyl-terminated polybutylene or fluorinated long-chain (thiol) alcohol and the like, wherein the solvent used is ethyl acetate, ethane or toluene and the like.

Although the super-amphiphobic performance is combined with the flame-retardant coating, the water and oil resistance of the flame-retardant coating can be greatly improved, the failure of the flame-retardant component caused by washing or oil contamination can be effectively reduced, and the application range of the flame-retardant coating is expanded and the practical performance of the coating is enhanced due to the characteristics of super-amphiphobic self-cleaning, oil contamination resistance, corrosion resistance and the like. However, since most low surface energy materials need to be dispersed in volatile organic solvents, a large amount of organic solvents are used in the preparation of flame retardant super-amphiphobic coatings. The preparation cost of the flame-retardant super-amphiphobic coating is increased, a large amount of Volatile Organic Substances (VOCs) and other waste gases are generated, and the serious threat is caused to the health safety and ecological environment of people. In addition, the volatility and the low ignition point of the organic matters cause the organic matters to be easily burnt or even exploded when meeting open fire, the potential safety hazard causes the storage and the transportation of the coating solution unchanged, and the practical application of the coating is greatly limited. When the material is applied outdoors, the material needs to be subjected to tests of weather such as ultraviolet irradiation, temperature change, wind, rain and the like, and the weather resistance of the coating is also extremely important. Therefore, aiming at the defects of the existing flame-retardant coating such as poor hydrophilicity and water resistance, oil stain resistance and the like, the prepared water-based flame-retardant coating with high weather resistance, super hydrophobicity and super lipophobicity has important environmental and economic significance for social development and daily life.

Disclosure of Invention

Aiming at the problems in the prior art, the invention provides a water-soluble flame-retardant super-amphiphobic coating, a preparation method and a coating, which can solve the problems of easy loss of active ingredients and poor weather resistance of the conventional flame-retardant coating and meet the requirements of flame retardance, fire resistance, water and oil resistance of the surface and long-term weather resistance of a flammable material.

The technical scheme adopted by the invention is as follows:

a water-soluble flame-retardant super-amphiphobic coating comprises the following components in percentage by weight:

0.1-5% of micro-nano particles, 0.1-5% of flame retardant, 0.4-20% of double-component low-surface-energy substance and the balance of solvent;

the two-component low surface energy substance comprises a component A and a component B, wherein the component A is a fluorine-containing or carbon-containing surfactant, and the component B is a fluorine-containing low surface energy substance; wherein the component A at least accounts for 10 percent of the mass of the two-component low surface energy substance.

Further, the micro-nano particles are one or a mixture of two or more of silicon dioxide, zinc oxide, titanium dioxide, aluminum oxide, aluminum nitride, magnesium oxide, magnesium hydroxide, cobalt hydroxide, zirconium oxide, silver sulfide, calcium carbonate, silver particles, graphene, carbon nanotubes, polyurea formaldehyde, polystyrene, polyacrylamide, polytetrafluoroethylene, polyvinylidene fluoride and polymethyl methacrylate in any proportion.

Further, the flame retardant is one or a mixture of two or more of ammonium polyphosphate, ethanolamine-modified ammonium polyphosphate, ethylenediamine-modified ammonium polyphosphate, propylenediamine-modified ammonium polyphosphate, piperazine-modified ammonium polyphosphate, ammonium polyphosphate derivatives, polyphosphates, ammonium phosphate salts, melamine polyphosphate salts, phosphate esters, hypophosphite, melamine cyanurate, melamine phosphate, melamine polyphosphate, antimony trioxide, dithiopyrophosphate, neopentyl dithiophosphate, tetraethyl orthosilicate, alkali metal ions, alkaline earth metal ions, transition metal ions, sodium metasilicate pentahydrate, polysilicic acid, polydimethylsiloxane, aluminum tripolyphosphate, tricresyl phosphate, triphenyl phosphite, dimethyl methylphosphonate and stannous zincate in any proportion.

Further, the component A is one or a mixture of two or more of acrylate emulsion, styrene-acrylic emulsion, silicone-acrylic emulsion, polyvinyl acetate-acrylic emulsion, polyurethane dispersion, ethylene-acrylic emulsion, polysorbate, sodium dodecyl sulfate, cetyl trimethyl ammonium bromide, fluorinated acrylic copolymer, fluorinated polyurethane copolymer, fluorine-containing nonionic surfactant, fluorine-containing anionic surfactant and fluorine-containing cationic surfactant in any proportion.

Further, the component B is one or a mixture of two or more of fluorooctyl dimethylchlorosilane, perfluorooctanoyl chloride, perfluoroheptanoic acid, perfluorooctanoic acid, polyperfluoroethylpropylene, perfluoroalkoxy, a perfluorinated cyclic polymer, p-trifluoromethoxyaniline and derivatives thereof, 4- (4-trifluoromethoxyphenylazo) phenol and derivatives thereof, fluorinated long-chain alcohol, fluorinated long-chain amine and a fluorine-containing silane coupling agent in any proportion; the fluorine-containing silane coupling agent has the following linear structural formula:

(CH₃O)₃Si(CH₂)₂(CF₂)nCF₃、

(CH₃CH₂O)₃Si(CH₂)₂(CF₂)nCF₃or

Cl₃Si(CH₂)₂(CF₂)nCF₃，

Wherein n is more than or equal to 1.

A preparation method of a water-soluble flame-retardant super-amphiphobic coating comprises the following steps:

step 1: dispersing the micro-nano particles, the flame retardant and the component A low-surface-energy substance in a solvent, and stirring for full reaction to obtain a dispersion liquid;

step 2: and (3) dispersing the component B low-surface-energy substance in the dispersion liquid obtained in the step (1), and continuously stirring and fully reacting to obtain the required water-soluble flame-retardant super-amphiphobic coating.

Further, the reaction time in the step 1 is 0.5-96 h.

Further, the reaction time in the step 2 is 0.5-96 h.

And coating the coating on a substrate to obtain the required coating.

Further, the coating method is one of a rolling baking method, a spraying method, a brushing method or a dipping method; the base material is one of a high polymer material base material, an inorganic non-metal material base material and a metal material base material.

The invention has the beneficial effects that:

(1) the water-soluble flame-retardant super-amphiphobic coating provided by the invention combines micro-nano particles, a flame retardant and a bi-component low-surface-energy substance, and realizes high flame retardance and super-amphiphobic property of the surface of the material through a multi-component synergistic effect;

(2) the water-soluble hydrophobic and oleophobic coating obtained by the invention has proper component content matching, and the optimal technical effect can be realized through the specially selected coating component content matching;

(3) the invention adopts bi-component low surface energy substance, the combination of the component A and the component B can synergistically reduce the surface energy of the coating, and the coating can be mixed with water in any proportion;

(4) the coating obtained by the invention can be used for various base materials such as wood building protection, living home and special protective clothing, can solve the problems of easy loss of effective components and poor weather resistance of the current flame-retardant coating, and meets the requirements of flammable materials on flame retardance, fire resistance, water and oil resistance of the surface, environmental protection, long-term weather resistance;

(5) the preparation method can not only enable the micro-nano particles to fully react with the low surface energy substance of the component A, but also endow the micro-nano particles with hydrophobic property, enable the modified micro-nano particles to be uniformly and compactly combined with the flame retardant, and enable the micro-nano particles, the flame retardant to be tightly connected with the low surface energy substances of the component A and the component B through covalent bonds, hydrogen bonds, electrostatic interaction, physical chelation and the like, so that the substances cannot be washed away by a solvent or mechanically scraped away, and the stability of the flame retardant and super-amphiphobic property of the coating can be ensured;

(6) the preparation method is simple, the raw materials are wide in source, the preparation conditions are mild, the water is used as a solvent, the environment is protected, the price is low, the large-scale production can be realized, and the industrial application and popularization are facilitated.

Drawings

FIG. 1 is an SEM scanning electron micrograph of the surface microstructure of the substrate (unmodified cotton) used in example 6.

FIG. 2 is an SEM scanning electron microscope image of the surface microstructure of the cotton cloth substrate modified by the water-soluble flame-retardant super-amphiphobic coating in example 6.

FIG. 3 is a schematic diagram showing the wettability of the surface of a substrate coated with a water-soluble flame-retardant super-amphiphobic coating prepared in example 5 by various liquid droplets.

FIG. 4 is a side view of the static contact angle of the surface of the substrate modified with the water-soluble flame retardant super-amphiphobic coating of example 1 with n-dodecane, edible oil and water.

FIG. 5 is a side view of the dynamic wettability of the surface of the water-soluble flame retardant super-amphiphobic coating modified substrate for water droplets, edible oil and n-dodecane in example 8.

FIG. 6 is a graph showing the flame retardant property of the cotton substrate modified with the water-soluble flame retardant super-amphiphobic coating and the unmodified cotton substrate in example 6.

Detailed Description

The invention is further described with reference to the following figures and specific embodiments.

The surface microstructure, hydrophobic and oleophobic properties, and the test methods used for vertical burning of coatings applied by the coatings prepared in the following examples and comparative examples are as follows:

SEM scanning electron microscope, observe the microstructure of the coating surface. And the contact angle tester is used for testing the hydrophobic and oleophobic performance of the coating surface. The flame retardant properties of the unmodified and modified cotton cloths were tested using a vertical combustion method using a horizontal vertical burner (CZF-3) according to the flame retardant test standards.

A water-soluble flame-retardant super-amphiphobic coating comprises the following components in percentage by weight:

0.1-5% of micro-nano particles, 0.1-5% of flame retardant, 0.4-20% of double-component low-surface-energy substance and the balance of solvent;

the two-component low surface energy substance comprises a component A and a component B, wherein the component A is a fluorine-containing or carbon-containing surfactant, and the component B is a fluorine-containing low surface energy substance; wherein the component A at least accounts for 10 percent of the mass of the two-component low surface energy substance.

The micro-nano particles are one or a mixture of two or more of silicon dioxide, zinc oxide, titanium dioxide, aluminum oxide, aluminum nitride, magnesium oxide, magnesium hydroxide, cobalt hydroxide, zirconium oxide, silver sulfide, calcium carbonate, silver particles, graphene, carbon nano tubes, polyurea aldehyde, polystyrene, polyacrylamide, polytetrafluoroethylene, polyvinylidene fluoride and polymethyl methacrylate in any proportion. The flame retardant is one or a mixture of two or more of ammonium polyphosphate, ethanolamine-modified ammonium polyphosphate, ethylenediamine-modified ammonium polyphosphate, propylenediamine-modified ammonium polyphosphate, piperazine-modified ammonium polyphosphate, ammonium polyphosphate derivatives, polyphosphate, ammonium phosphate salts, melamine polyphosphate, phosphate esters, hypophosphite, melamine cyanurate, melamine phosphate esters, melamine polyphosphate, antimony trioxide, dithiophosphoric acid, neopentyl dithiophosphate, tetraethyl orthosilicate, alkali metal ions, alkaline earth metal ions, transition metal ions, sodium metasilicate pentahydrate, polysilicic acid, polydimethylsiloxane, aluminum tripolyphosphate, tricresyl phosphate, triphenyl phosphite, dimethyl methylphosphonate and stannous zincate in any proportion. The component A is one or a mixture of two or more of acrylate emulsion, styrene-acrylic emulsion, silicone-acrylic emulsion, polyvinyl acetate-acrylic emulsion, polyurethane dispersion, ethylene-acrylic emulsion, polysorbate, sodium dodecyl sulfate, cetyl trimethyl ammonium bromide, fluorinated acrylic copolymer, fluorinated polyurethane copolymer, fluorine-containing nonionic surfactant, fluorine-containing anionic surfactant and fluorine-containing cationic surfactant in any proportion. The component B is one or a mixture of two or more of fluorooctyl dimethylchlorosilane, perfluorooctanoic acid chloride, perfluoroheptanoic acid, perfluorooctanoic acid, polyperfluoroethylpropylene, perfluoroalkoxy, a perfluorinated cyclic polymer, p-trifluoromethoxyaniline and derivatives thereof, 4- (4-trifluoromethoxyphenylazo) phenol and derivatives thereof, fluorinated long-chain alcohol, fluorinated long-chain amine and a fluorine-containing silane coupling agent in any proportion; the fluorine-containing silane coupling agent has the following linear structural formula:

(CH₃O)₃Si(CH₂)₂(CF₂)nCF₃、

(CH₃CH₂O)₃Si(CH₂)₂(CF₂)nCF₃or

Cl₃Si(CH₂)₂(CF₂)nCF₃，

Wherein n is more than or equal to 1. The fluorine-containing silane coupling agent in the component B is preferably one or a mixture of two or more of perfluorodecyltrimethoxysilane, perfluorodecyltriethoxysilane, perfluorodecyltrichlorosilane, perfluorooctyltrimethoxysilane, perfluorooctyltriethoxysilane, perfluorooctyltrichlorosilane and perfluorohexyltrichlorosilane in any proportion.

A preparation method of a water-soluble flame-retardant super-amphiphobic coating comprises the following steps:

step 1: dispersing the micro-nano particles, the flame retardant and the component A low-surface-energy substance in a solvent, and stirring for reaction for 0.5-96 h to obtain a dispersion liquid;

step 2: and (3) dispersing the component B low-surface-energy substance in the dispersion liquid obtained in the step (1), and continuously stirring for reaction for 0.5-96 h to obtain the required water-soluble flame-retardant super-amphiphobic coating.

And coating the paint on a base material to obtain the required coating. The coating method is one of rolling baking, spraying, brushing or dipping; the base material is one of a high polymer material base material, an inorganic non-metal material base material and a metal material base material. The coating is coated on the surface of a substrate, so that the flame-retardant super-amphiphobic coating can be obtained, and the flame-retardant performance and the super-amphiphobic performance are endowed to the substrate. The preparation method can be widely applied to the fields of preparing flame-retardant and anti-corrosion bamboo building materials, protective clothing, multifunctional and intelligent textiles, food packaging, liquid transportation, marine antifouling, medical instruments, self-cleaning and anti-corrosion materials, building exterior walls, movable or immovable cultural relic protection and the like. The substrate may be any one of natural fibers such as cotton, hemp, silk, wool, regenerated cellulose fibers such as viscose, lyocell, modal, tencel, regenerated protein fibers, synthetic fibers, fabrics and textiles, wood, bamboo, flexible foams, sponges, glass, stone, cement boards, ceramics, steel, copper, iron, aluminum, polyvinylidene fluoride films, polyethylene terephthalate films, rubber, cellulose films, or paper products.

During the specific coating application process of the coating, the adhesive can be alternatively coated to increase the stability of the coating, so that the coating can be stably adhered to the surface of the substrate.

Example 1

The water-soluble flame-retardant super-amphiphobic coating is prepared according to the following steps:

step 1: 0.09g of the mixed zinc oxide particles, magnesium hydroxide particles, silver sulfide and tin sulfide particles, 1.37g of ethanolamine-modified ammonium polyphosphate flame retardant and 5g of sodium dodecyl sulfate are ultrasonically dispersed into a solvent consisting of 30g of water and 13.02g of acetone, and stirred for reaction for 18 hours.

Step 2: and (3) dispersing a component B low-surface-energy substance formed by mixing 0.52g of fluorinated ethylene propylene and perfluoroalkoxy into the dispersion liquid obtained in the step (1), and stirring and reacting for 36 hours to obtain the water-soluble flame-retardant super-amphiphobic coating.

Wherein the zinc oxide particles, magnesium hydroxide particles, silver sulfide particles, and tin sulfide particles have an average size of about 300 nanometers.

The coating obtained in the embodiment is coated on the surface of the viscose fiber by a rolling baking method, and the flame-retardant super-amphiphobic coating can be obtained after the coating is dried.

The resulting static contact angle test pattern for n-dodecane, edible oil and water is shown in fig. 4. As can be seen from the figure, the static contact angles of the surface of the coating to n-dodecane, edible oil and water are all higher than 150 degrees, the rolling angles are all lower than 5 degrees, and the coating has excellent super-hydrophobic and super-oleophobic properties. The resulting modified viscose fiber passed the vertical burn test, i.e., no bright flame was generated when lit for 12s, and quickly self-extinguished after removal of the burner, leaving only about 10cm of carbon residue, with the remainder remaining intact.

Example 2

The water-soluble flame-retardant super-amphiphobic coating is prepared according to the following steps:

step 1: 0.05g of mixed magnesium hydroxide particles and magnesium oxide particles, 0.05g of flame retardant formed by mixing phosphate, hypophosphite and melamine and 0.3g of fluorinated polyurethane copolymer are ultrasonically dispersed in a solvent formed by 35.5g of water and 11.4g of n-acetone, and stirred for reaction for 36 hours.

Step 2: and (3) dispersing a component B low-surface-energy substance formed by mixing 2.7g of perfluorodecyl trichlorosilane and perfluorooctyl trimethoxysilane into the dispersion liquid obtained in the step (1), and stirring for reaction for 12 hours to obtain the water-soluble flame-retardant super-amphiphobic coating.

Wherein the magnesium hydroxide particles and the magnesium oxide particles have an average size of about 200 nanometers.

The coating prepared by the embodiment is coated on the surface of wood in a dip-coating mode, and the flame-retardant super-amphiphobic surface can be obtained after the coating is dried.

The contact angles of the coating obtained in this example for water, glycerol, paraffin oil and n-dodecane were 162.5 °, 160.5 °, 158.5 ° and 153.2 °, respectively, and the rolling angles were below 10 °. The resulting modified wood was self-extinguishing by vertical burn testing, i.e., after 10 seconds of ignition, leaving only about 10cm of residual carbon, with the remainder remaining intact. The substrate can be replaced by various substrates such as bamboo, soft foam, cellulose membrane, paper product, etc.

Example 3

The water-soluble flame-retardant super-amphiphobic coating is prepared according to the following steps:

step 1: 2.5g of polyurea-formaldehyde and polyurea particles, 2.5g of antimony trioxide, dithio pyrophosphate and neopentyl dithiophosphate are mixed to form a flame retardant, 0.1g of acrylate emulsion and styrene-acrylic emulsion are mixed to form a component A low surface energy substance, the low surface energy substance is ultrasonically dispersed into a mixed solvent consisting of 20g of water and 24.8g of water, and the mixture is stirred and reacted for 48 hours.

Step 2: and (3) dispersing 0.1g of a component B low-surface-energy substance consisting of perfluorooctyl triethoxysilane and perfluorooctyl trichlorosilane into the dispersion liquid obtained in the step (1), and stirring for reacting for 36 hours to obtain the water-soluble flame-retardant super-amphiphobic coating.

Wherein the average size of the polyurea-urea-formaldehyde and polyurea particles is about 300 microns.

The water-soluble flame-retardant super-amphiphobic coating obtained in the embodiment is coated on the surface of glass by a brush coating method, and the glass surface is dried in a drying oven at the temperature of 45 ℃ to obtain the super-amphiphobic surface.

The contact angles of the coating obtained in this example for water, glycerol, diesel and n-hexadecane were 160.5 °, 159.45 °, 154.5 ° and 152 °, respectively, and the sliding angles were below 10 °. In addition, the glass substrate may be replaced by various substrates such as stone, cement board, and ceramics.

Example 4

The water-soluble flame-retardant super-amphiphobic coating is prepared according to the following steps:

step 1: 1.38g of mixed particles of aluminum oxide and aluminum nitride, 2.36g of flame retardant formed by mixing polysilicic acid, polydimethylsiloxane and aluminum tripolyphosphate and 0.42g of low surface energy substance of component A formed by mixing polyvinyl acetate acrylate emulsion, polyurethane dispersion liquid and ethylene acrylate emulsion are ultrasonically dispersed into a mixed solvent formed by 15.06g and 30g of isopropanol and stirred for reaction for 96 hours.

Step 2: and (3) dispersing a component B low-surface-energy substance formed by mixing 0.78g of perfluoroheptanoic acid and perfluorooctanoic acid into the dispersion liquid obtained in the step (1), and stirring for reacting for 20 hours to obtain the required water-soluble flame-retardant super-amphiphobic coating.

Wherein the aluminum hydroxide and aluminum nitride particles have an average size of about 500 nanometers.

The water-soluble flame-retardant super-amphiphobic coating prepared by the embodiment is coated on the surface of a polyethylene terephthalate film in a brush coating mode, and the polyethylene terephthalate film is dried in a drying oven at 80 ℃ to obtain the flame-retardant super-amphiphobic coating.

The contact angle of the coating obtained by the embodiment to various liquid drops including water, edible oil and paraffin oil is more than 150 degrees, and the rolling angle is less than 10 degrees. In addition, the obtained modified film can be self-extinguished within 10s after being ignited on an alcohol lamp for 5s, and the flame retardant property of the modified film is obviously improved.

The base material can be replaced by various base materials such as polyvinylidene fluoride film and rubber base material.

Example 5

The water-soluble flame-retardant super-amphiphobic coating is prepared according to the following steps:

step 1: 2.3g of titanium dioxide, cobalt hydroxide and zirconium oxide particles, 0.08g of flame retardant formed by mixing melamine cyanurate, melamine phosphate and melamine polyphosphate and 4.5g of a component A low surface energy substance formed by mixing polysorbate, silicone-acrylic emulsion and polyvinyl acetate emulsion are ultrasonically dispersed into a mixed solvent formed by 30g of water and 8.22g of n-hexane, and the mixture is stirred and reacted for 0.5 hour.

Step 2: and (3) dispersing a component B low-surface-energy substance formed by mixing 4.9g of fluorooctyl dimethylchlorosilane, perfluorooctanoyl chloride and perfluorodecyl trimethoxy silane into the dispersion liquid obtained in the step (1), and stirring for reaction for 48 hours to obtain the water-soluble flame-retardant super-amphiphobic coating.

Wherein the average size of the titania, cobalt hydroxide, and zirconia particles is about 500 nanometers.

The water-soluble flame-retardant super-amphiphobic coating obtained in the embodiment is coated on the surface of a copper mesh in a spraying mode, and is dried in a 45 ℃ oven, so that the flame-retardant super-amphiphobic coating can be obtained.

The contact angle of the coating obtained by the embodiment to various liquid drops including water, artificial blood, edible oil, paraffin oil, n-hexadecane, n-dodecane and the like is more than 150 degrees, and the rolling angle is less than 10 degrees. As shown in FIG. 3, it can be seen that various droplets are spherical on the surface of the coating and do not wet the substrate, so that the modified substrate has excellent super-hydrophobic and super-oleophobic properties.

Example 6

The water-soluble flame-retardant super-amphiphobic coating is prepared according to the following steps:

step 1: 0.5g of nano silicon dioxide, 0.50g of ammonium polyphosphate flame retardant and 1.0g of fluorinated acrylic copolymer are ultrasonically dispersed into 47g of water, and stirred for reaction for 24 hours.

Step 2: and (3) dispersing 1.0g of perfluorodecyl triethoxysilane into the dispersion liquid obtained in the step (1), and stirring for reaction for 10 hours to obtain the water-soluble flame-retardant super-amphiphobic coating.

Wherein the nanosilica particles have an average size of about 15 nm.

The coating obtained in the embodiment is sprayed on cotton cloth, and the flame-retardant super-amphiphobic coating can be obtained after the coating is dried at room temperature.

The scanning electron micrograph is shown in FIG. 2. Fig. 1 is an SEM scanning electron micrograph of the microstructure of the unmodified cotton surface. As can be seen from fig. 1, the unmodified cotton fiber surface was smooth and flat.

As can be seen from fig. 2, the surface of the well-modified cotton cloth becomes rougher due to the micro-nano multilevel structure, and the micro-nano multilevel structure constructed by the well-modified cotton cloth can be uniformly attached to the surface of the fiber to wrap the smooth fiber. The roughness of the surface of the cotton cloth fiber is obviously improved. The coating obtained by the embodiment can successfully modify cotton cloth and endow the cotton cloth with a micro-nano multilevel structure, so that more air is captured to improve the super-amphiphobic performance of the surface of the modified cotton cloth.

The contact angle of the coating surface obtained by the embodiment to various liquid drops including water, glycerin, edible oil, n-hexadecane, n-dodecane and the like is more than 150 degrees, and the rolling angle is less than 10 degrees. The flame retardant performance test is shown in fig. 6. It can be seen from the figure that the left side is the unmodified cotton test result and the right side is the modified cotton test result. The unmodified cotton cloth substrate was completely burnt directly, and the flame retardant performance of the modified cotton cloth was significantly improved, i.e. after the vertical combustion ignition for 12s and the burner was removed, the modified cotton cloth only left about 8cm of carbon residue, and the rest remained intact.

Example 7

The water-soluble flame-retardant super-amphiphobic coating is prepared according to the following steps:

step 1: 1.25g of polypropylene and polyurea-formaldehyde particles, 1.5g of flame retardant formed by mixing ethylenediamine modified ammonium polyphosphate, propylenediamine modified ammonium polyphosphate and piperazine modified ammonium polyphosphate, and 5g of hexadecyl trimethyl ammonium bromide are ultrasonically dispersed into a mixed solvent formed by 20g of water, 7.25g of petroleum ether and 10g of acetone, and are stirred and reacted for 20 hours.

Step 2: and (3) dispersing 5g of perfluoro cyclic polymer into the dispersion liquid obtained in the step (1), and stirring to react for 0.5h to obtain the water-soluble flame-retardant super-amphiphobic coating.

Wherein the average size of the mixed polystyrene and polyurea-formaldehyde particles is about 500 microns.

The coating obtained by the embodiment is coated on the surface of a polyvinylidene fluoride membrane in a spraying mode, and the coating is dried at room temperature to obtain the flame-retardant super-amphiphobic coating.

The coating obtained in this example has a contact angle of more than 150 ° and a sliding angle of less than 10 ° for a variety of droplets including water, n-hexadecane, n-dodecane, and the like. The obtained modified film material has no bright flame in the process of being continuously exposed to the flame of the alcohol lamp for 8s, and can be quickly self-extinguished after the alcohol lamp is removed, so that the modified film material has better flame retardant property.

Example 8

The water-soluble flame-retardant super-amphiphobic coating is prepared according to the following steps:

step 1: 1.98g of polyacrylamide, polytetrafluoroethylene and polyvinylidene fluoride particles, 0.98g of flame retardant formed by mixing ammonium polyphosphate derivatives, polyphosphate, ammonium phosphate and melamine polyphosphate, and 1.27g of fluorine-containing cationic surfactant are ultrasonically dispersed into a mixed solvent formed by 20g of water, 13.85g of glycerol and 10g of n-propanol, and are stirred and reacted for 18 hours.

Step 2: and (3) dispersing 1.92g of p-trifluoromethoxyaniline and derivatives thereof into the dispersion liquid obtained in the step (1), and stirring for reaction for 48 hours to obtain the water-soluble flame-retardant super-amphiphobic coating.

Wherein the average particle size of the mixed polyacrylamide, polytetrafluoroethylene and polyvinylidene fluoride particles is about 90 microns.

The coating obtained in the embodiment is coated on the surface of linen fabric by brushing, and the flame-retardant super-amphiphobic coating can be obtained after the coating is dried in a 45 ℃ oven.

The contact angle of the flame-retardant super-amphiphobic coating obtained by the embodiment to various liquid drops including water, edible oil, paraffin oil, diesel oil, hexadecane, glycerol and the like is more than 150 degrees, and the rolling angle is less than 10 degrees. The obtained test chart of the dynamic wettability of the coating to n-dodecane, edible oil and water is shown in figure 5, the rolling angles of the coating are all lower than 10 degrees, and the coating has excellent super-hydrophobic, super-oleophobic and self-cleaning performances. In addition, after the flame-retardant alcohol lamp is ignited on an alcohol lamp for 12 seconds, the flame-retardant alcohol lamp can be quickly self-extinguished within 5 seconds, and has excellent flame-retardant performance. And the air permeability, the surface color and the texture of the linen fabric are not influenced by the coating after the linen fabric is modified.

Example 9

The water-soluble flame-retardant super-amphiphobic coating is prepared according to the following steps:

step 1: 0.9g of graphene, carbon nano tubes, calcium carbonate and aluminum hydroxide particles, 1.14g of flame retardant formed by mixing tetraethyl orthosilicate, alkali metal ions, alkaline earth metal ions, transition metal ions and sodium metasilicate pentahydrate and 4.61g of fluorine-containing anionic surfactant are ultrasonically dispersed into a mixed solvent formed by 30g of water and 11.18g of butyl acetate, and are stirred and reacted for 30 hours.

Step 2: and (3) dispersing 2.17g of 4- (4-trifluoromethoxyphenyl azo) phenol into the dispersion liquid obtained in the step (1), and stirring to react for 96 hours to obtain the water-soluble flame-retardant super-amphiphobic coating.

Wherein the average size of the mixed graphene, carbon nanotubes, calcium carbonate and aluminum hydroxide particles is about 500 nanometers.

The coating obtained in the embodiment is coated on the surface of the cellulose membrane in a spraying mode, and the flame-retardant super-amphiphobic coating can be obtained after natural airing.

The contact angles of the flame-retardant super-amphiphobic coating obtained by the embodiment to various liquid drops including water, edible oil, paraffin oil, diesel oil, hexadecane, glycerol and the like are all 150 degrees, and the rolling angle is less than 10 degrees. The obtained modified cellulose membrane can be quickly self-extinguished within 7s after being ignited on an alcohol lamp for 10s, and has excellent flame retardant property.

Example 10

The water-soluble flame-retardant super-amphiphobic coating is prepared according to the following steps:

step 1: 2.1g of silver particles, polyacrylamide and polymethyl methacrylate particles, 1.79g of flame retardant formed by mixing tricresyl phosphate, triphenyl phosphite, dimethyl methylphosphonate and stannous zincate, and 4.93g of fluorine-containing nonionic surfactant are ultrasonically dispersed into a mixed solvent formed by 28.62g of water, 5g of cyclohexane and 5g of toluene, and are stirred for reaction for 30 hours.

Step 2: and (3) dispersing a component B low-surface-energy substance formed by mixing 2.56g of fluorinated long-chain alcohol and fluorinated long-chain amine into the dispersion liquid obtained in the step (1), and stirring for reacting for 24 hours to obtain the water-soluble flame-retardant super-amphiphobic coating.

Wherein the silver particles, polyacrylamide and polymethylmethacrylate particles have an average size of about 10 microns.

The coating obtained in the embodiment is coated on the surface of the sponge in a dip-coating mode and is dried in a 45 ℃ oven to obtain the flame-retardant super-amphiphobic coating.

The contact angle of the coating obtained by the embodiment is more than 150 degrees and the rolling angle is less than 10 degrees for various liquid drops including water, edible oil, paraffin oil, diesel oil, hexadecane, glycerol and the like.

The obtained modified sponge has no bright flame after being ignited on an alcohol lamp for 20s, can be quickly self-extinguished within 5s, and has excellent flame retardant property. Moreover, the color and texture of the modified sponge are not affected by the coating.

The water-soluble flame-retardant super-amphiphobic coating disclosed by the invention combines micro-nano particles, a flame retardant and a multi-component low-surface-energy substance, and realizes high-efficiency flame retardance and super-amphiphobic property of the surface of the material through a synergistic effect of two components. Micro-nano particles, a flame retardant and a bi-component low surface energy substance in the coating are used as the surface structure construction elements of the coating. Through reasonable process and component proportion, a micro-nano synergetic concave suspension structure is formed on the surface of the base material in situ, and the structure can capture a large amount of air and form an air film, effectively prevent liquid from contacting and wetting, and improve the hydrophobic and oleophobic performances of the surface of the obtained coating. And the bi-component low surface energy substance in the coating can enable the coating to be mixed with water in any proportion, so that the surface energy of the coating is effectively reduced, and on one hand, the hygroscopicity of the flame retardant is improved, and the flame retardance of the coating is more durable. On the other hand, the combination of the low surface energy substance and the micro-nano concave rough structure can realize excellent super-amphiphobic performance of the surface of the base material. And the content proportion of each component in the coating is proper, and the optimal technical effect is realized through the specially selected content proportion of the coating components. If the mass percentage of the micro-nano particles and the flame retardant is higher than the limited mass percentage range, the micro-nano particles and the flame retardant cannot be completely dissolved to form a uniform solution, so that the spraying is not uniform, and the technical effect cannot be achieved. If the amount of the multi-component low surface energy material is less than the defined mass range, the coating is caused to have only hydrophobic and flame retardant properties and not super hydrophobic and super oleophobic properties.

The two-component low surface energy material used in the coating of the present invention comprises a component A and a component B. The component A low surface energy substance is a fluorine-containing or carbon-containing surfactant which simultaneously contains hydrophilic and hydrophobic chemical structures. On one hand, the hydrophilic structure part of the A component low surface energy substance can enable the micro-nano particles and the flame retardant to be uniformly dispersed in water, and on the other hand, the hydrophobic structure part of the A component low surface energy substance can reduce the surface energy of the micro-nano particles and the flame retardant and enhance the hydrophobic performance of the micro-nano particles and the flame retardant. The component B is a fluorine-containing low surface energy substance, and the molecular structure of the component B contains a long carbon chain or a long fluorine chain structure, so that the effect of reducing the surface energy of the coating can be further achieved, and the hydrophobic and oleophobic properties of the coating can be further enhanced. The combination of the low surface energy substances of the component A and the component B can play a role in synergistically reducing the surface energy of the coating, so that the coating can be mixed with water in any proportion. If the amount of the A component in the multi-component low surface energy material is less than the defined range, the coating material may not be uniformly dissolved in water, resulting in increased cost and environmental pollution.

The coating obtained by the preparation method can ensure that the micro-nano particles can fully react with the low surface energy substance of the component A and endow the micro-nano particles with hydrophobic property, so that the modified micro-nano particles can be uniformly and compactly combined with the flame retardant, and the micro-nano particles, the flame retardant and the low surface energy substances of the component A and the component B can be tightly connected through covalent bonds, hydrogen bonds, electrostatic interaction, physical chelation and the like, so that the micro-nano particles and the flame retardant can not be washed away by a solvent or mechanically scraped away, and the flame retardant super-amphiphobic stability of the coating is ensured.

The coating obtained by the invention can be used for various base materials such as wood building protection, living home and special protective clothing, and the like, and solves the problems of easy loss of effective components and poor weather resistance of the conventional flame-retardant coating. Meets the requirements of flame retardance and fire prevention of flammable materials, water and oil resistance of the surface and long-term weather resistance of environmental protection. The preparation method of the coating is simple, the raw materials are wide in source, the preparation conditions are mild, the water is used as a solvent, the environment is protected, the price is low, the large-scale production can be realized, and the industrial application and popularization are facilitated.