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Amphiphilic cross-linked fluoropolymer and application thereof in preparation of ultra-amphiphobic surface

A super-amphiphobic surface and polymer technology, applied in the manufacture of tools, coatings, paper coatings, etc., can solve the problem of non-toxic and environmentally friendly solvent dispersants, weak adhesion between fluoropolymers and substrate surfaces, etc. problem, to achieve the effect of simple method and firm bonding

Active Publication Date: 2014-07-30
GUANGZHOU CHEM CO LTD CHINESE ACADEMY OF SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0010] In order to overcome the defects of weak adhesion between the existing fluoropolymer and the surface of the substrate and the inability to use non-toxic and environmentally friendly solvents as dispersants, the primary purpose of the present invention is to provide an amphiphilic cross-linkable Fluoropolymer

Method used

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  • Amphiphilic cross-linked fluoropolymer and application thereof in preparation of ultra-amphiphobic surface
  • Amphiphilic cross-linked fluoropolymer and application thereof in preparation of ultra-amphiphobic surface
  • Amphiphilic cross-linked fluoropolymer and application thereof in preparation of ultra-amphiphobic surface

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0051] ATRP synthesis of amphiphilic cross-linkable fluoropolymers comprises the following steps:

[0052] Add 1.852g trifluoroethyl methacrylate, 0.203g monomethoxyethylene glycol 2-bromoisobutyrate, 0.237g 4,4'-dinonyl-2,2' into a 100ml round bottom flask - bipyridine and 3ml anisole, the reaction system was stirred and dissolved, and the argon bubble was bubbled for 30min, and then the oxygen was removed, and then the reaction system was transferred to a 50ml round bottom flask with 0.1124g cuprous bromide, at 40 The polymerization reaction was carried out at ℃ for 2 hours, and the reaction product was precipitated in methanol, washed with methanol and then washed with n-hexane, and then vacuum-dried at room temperature for 24 hours to constant weight to obtain the product PTFEMA-Br.

[0053] In a 100ml round bottom flask, add 1.5g polytrifluoroethyl methacrylate (PTFEMA-Br) synthesized above, 1.052g glycidyl methacrylate (GMA), 1.252g polyethylene glycol glycidyl methacryl...

Embodiment 2

[0062] Synthesis of amphiphilic cross-linkable fluoropolymer by anionic polymerization, comprising the following steps:

[0063] At -78°C (dry ice acetone bath), add 0.19 ml of 1,1-diphenylethylene to a three-necked flask containing 250 ml of anhydrous tetrahydrofuran, followed by adding 0.6 ml of 1.4 mol / L sec-butyllithium in hexyl alkane solution. After 25 minutes, 25.19 milliliters of pentafluoroethyl methacrylate was added, and 21.24 milliliters of glycidyl acrylate (GA) and 25 polyethylene glycol methacrylate (PEGMA) were added at the same time after the polymerization reaction was carried out for 1 hour, and the polymerization reaction continued for another 2 hours. After 1 hour, 1.0 ml of anhydrous methanol was added to terminate the polymerization. After the reaction system was heated to 23°C, it was concentrated by distillation to 100 ml, and then the polymer was precipitated in excess methanol, filtered and dried in a vacuum oven to obtain the desired polymer PFEMA-...

Embodiment 3

[0072] Synthesis of amphiphilic cross-linkable fluoropolymers using the "Click" method, including the following steps:

[0073] Add 2.852g of pentafluoroethyl methacrylate, 0.103g of trimethylsilyl ATRP initiator, 0.237g of 4,4'-dinonyl-2,2'-bipyridine and 3ml of benzyl in a 100ml round bottom flask Ether, stirring and dissolving the reaction system, bubbling with argon gas for 30min, then deoxygenating, then transferring the reaction system to a 100ml round-bottomed flask containing 0.1124g of cuprous bromide, and carrying out the polymerization reaction at 40°C for 2h, the reaction The product was precipitated in methanol, washed with methanol and then washed with n-hexane, and then vacuum-dried at room temperature for 24 h to constant weight to obtain PFEMA with an alkynyl terminal.

[0074] Add 0.15g monomethoxyethylene glycol 2-bromoisobutyrate, 1.852g glycidyl methacrylate and 1.125g polyethylene glycol methyl methacrylate, 0.737g 4 in a 100ml round bottom flask, 4'-Din...

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Abstract

The present invention discloses an amphiphilic cross-linked fluoropolymer and application thereof. The amphiphilic cross-linked fluoropolymer has a general formula shown below, wherein, polymerization degree of an A segment is 40-1000, polymerization degree of a B segment is 10-100, polymerization degree of a C segment is 20-400; the chain segment A is polymerized by monomer as, the chain segment B is polymerized by monomer bs, and the chain segment C is polymerized by monomer cs. The amphiphilic cross-linked fluoropolymer prepared by the present invention has an epoxy group. Therefore the advantage that the epoxy group has an adhesive force with vast majority surfaces of substrates can be used, and an ultra-amphiphobic surface can be constructed on the vast majority of the substrates. The oxysilane in the present invention is a group which can make a crosslinking reaction with the substrate having the surfaces grafted with active groups such as hydroxy, amino or carboxyl, so the fluoropolymer can also make crosslinking reaction with the vast majority of the substrate surfaces. The amphiphilic cross-linked fluoropolymer of the present invention overcome the defects that the adhesive force between the conventional fluoropolymers and the surfaces of the substrates is not strong, and non-toxic environmental-friendly solvents cannot be dispersants. A-B-(B-r-C).

Description

technical field [0001] The invention belongs to the field of super-amphiphobic materials, in particular to an amphiphilic cross-linkable fluorine-containing polymer and its application in preparing super-amphiphobic surfaces. Background technique [0002] Due to its unique hydrophobic and oleophobic properties, superamphiphobic surfaces can be applied in many fields. The superamphiphobic surface has a self-cleaning function and can be used for solar panels or some mirrors that need to be kept clean, such as the surface of a gas cooker. Furthermore, the formation of a superamphiphobic surface on the metal surface can also greatly improve the corrosion resistance of the metal surface. In addition, if a super-amphiphobic surface is built on the wire or high-voltage power grid, it can prevent the wire from forming a frozen layer on the surface of the ice storm or snowstorm, which will cause a short circuit and cause a large-scale power outage to stop production, and even lead t...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08F293/00C08F220/24C08F224/00C08F220/28C08G81/02C09D153/00C09D133/16C09D187/00C09D5/08D06M15/37D21H19/20D21H19/24B27K3/36
Inventor 胡继文邹海良张干伟刘锋侯成敏杨洋李妃
Owner GUANGZHOU CHEM CO LTD CHINESE ACADEMY OF SCI