Preparation method of durable photo-thermal real-time self-repairing super-amphiphobic coating

A self-healing, super-amphiphobic technology, applied in coatings and other directions, can solve problems such as poor durability

CN113388293AActive Publication Date: 2021-09-14LANZHOU INST OF CHEM PHYSICS CHINESE ACAD OF SCI
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Patent Information

Authority / Receiving Office
CN · China
Current Assignee / Owner
Publication Date
2021-09-14
Patent Text Reader

Abstract

The invention discloses a preparation method of a durable photo-thermal real-time self-repairing super-amphiphobic coating, which comprises the steps of synthesizing a styrene / styrene derivative-bisphenol A diglycidyl ether monoacrylate copolymer capable of generating a steam-induced phase separation function through ring-opening reaction, free radical polymerization and cross-linking reaction, wherein the copolymer has a bonding effect, a self-repairing effect and a micron 'armor' protection effect generated by phase separation, so that the coating is endowed with excellent durability; and introducing fluorinated carbon nanotubes with excellent photo-thermal effect and heat-conducting property into a self-repairing polymer so as to endow the coating with excellent super-amphiphobic property, durability and real-time photo-thermal self-repairing property, and then obtaining the durable photo-thermal real-time self-repairing super-amphiphobic coating through steam-induced phase separation and curing crosslinking. According to the coating, real-time self-repairing of the super-amphiphobic coating on micro-nano structure damage and chemical damage can be achieved by means of sunlight, and a solid foundation is laid for practical application of the super-amphiphobic coating.
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Description

technical field

[0001] The invention relates to the preparation of a super-amphiphobic coating, in particular to a method for preparing a durable photothermal real-time self-repairing super-amphiphobic coating, which belongs to the field of super-amphiphobic coatings. Background technique

[0002] Superamphiphobic coating is a special wettability surface with contact angles greater than 150° and low rolling angle for water and low surface energy liquids such as oil. Due to its unique wetting properties, it has broad application prospects and potential economic value in the fields of self-cleaning, anti-icing, anti-fouling, oil / water separation, and anti-corrosion. The preparation ideas of super-amphiphobic coatings mainly fall into the following three categories: (1) construct rough structure first and then perform low surface energy treatment; (2) construct rough structure after low surface energy treatment; (3) construct rough structure and low surface energy Surface ener...

Examples

Embodiment 1

[0033] (1) Dissolve bisphenol A diglycidyl ether in toluene by heating at 70°C; then dissolve potassium hydroxide in acrylic acid and add it dropwise to the toluene solution of bisphenol A diglycidyl ether, and add inhibitor Polymer hydroquinone, reflux reaction at 110~120°C for 48~60 h (nitrogen protection), the product is separated and purified by column chromatography to obtain bisphenol A diglycidyl ether monoacrylate, in which bisphenol A The molar ratio of diglycidyl ether and acrylic acid is 1:1, the amount of hydroquinone added is 0.3% of the total mass of bisphenol A diglycidyl ether and acrylic acid, and the amount of potassium hydroxide added is 0.6% of the mass of acrylic acid. Then take bisphenol A diglycidyl ether monoacrylate and styrene into a three-necked flask filled with tetrahydrofuran, add the initiator azobisisobutyronitrile, and react at 70°C for 48 h under reflux (nitrogen protection) to obtain styrene- Bisphenol A diglycidyl ether monoacrylate copolyme...

Embodiment 2

[0038] (1) Dissolve bisphenol A diglycidyl ether in toluene by heating at 70°C; then dissolve potassium hydroxide in acrylic acid and add it dropwise to the toluene solution of bisphenol A diglycidyl ether, and add inhibitor Polymerizing agent hydroquinone, reflux reaction at 110~120°C for 48~60 h (nitrogen protection), the product is separated and purified by column chromatography to obtain bisphenol A diglycidyl ether monoacrylate, in which bisphenol A The molar ratio of diglycidyl ether and acrylic acid is 1:0.75, the amount of hydroquinone added is 0.24% of the total mass of bisphenol A diglycidyl ether and acrylic acid, and the amount of potassium hydroxide added is 0.5% of the mass of acrylic acid. Then take bisphenol A diglycidyl ether monoacrylate and styrene into a three-necked flask filled with tetrahydrofuran, add the initiator azobisisobutyronitrile, and react under reflux at 70°C for 48 h (nitrogen protection) to obtain styrene- Bisphenol A diglycidyl ether monoac...

Embodiment 3

[0043] (1) Dissolve bisphenol A diglycidyl ether in toluene by heating at 70°C; then dissolve potassium hydroxide in acrylic acid and add it dropwise to the toluene solution of bisphenol A diglycidyl ether, and add inhibitor Polymerizing agent hydroquinone, reflux reaction at 110~120°C for 48~60 h (nitrogen protection), the product is separated and purified by column chromatography to obtain bisphenol A diglycidyl ether monoacrylate, in which bisphenol A The molar ratio of diglycidyl ether and acrylic acid is 1:1, the amount of hydroquinone added is 0.3% of the total mass of bisphenol A diglycidyl ether and acrylic acid, and the amount of potassium hydroxide added is 0.6% of the mass of acrylic acid. Then take bisphenol A diglycidyl ether monoacrylate and styrene into a three-necked flask filled with tetrahydrofuran, add the initiator azobisisobutyronitrile, and react under reflux at 70°C for 48 h (nitrogen protection) to obtain styrene- Bisphenol A diglycidyl ether monoacryla...