Water-dispersible crosslinking type fluoropolymer and application of fluoropolymer in preparation of super-amphiphobic surfaces
A super-amphiphobic surface and dispersive technology, which is applied in the manufacture of tools, coatings, paper coatings, etc., can solve the problems of endangering human health, polluting the environment, and the high price of fluoropolymers, achieving reliable bonding and simple methods Effect
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Embodiment 1
[0050] The ATRP method synthesizes water-dispersible cross-linkable fluoropolymer, comprising the following steps:
[0051] (1) Synthesis of monomer Epoxy-PEGMA 526
[0052] Add 2.5g polyethylene glycol methacrylate (Mn=500) and 12ml epichlorohydrin to toluene, then add catalyst boron trifluoride-ether mixed solution and sodium hydroxide, react at 20°C for 2 hours , after washing and precipitation, polyethylene glycol methacrylate with epoxy group at the end (that is, Epoxy-PEGMA 526 ); wherein the mass ratio of polyethylene glycol methyl methacrylate, epichlorohydrin, toluene, boron trifluoride-ether and sodium hydroxide is 1:0.5:10:0.01:0.01.
[0053] The above process takes place as follows:
[0054]
[0055] (2) Synthesis of water-dispersible cross-linkable fluoropolymer
[0056] Add 1.852g of monomer Epoxy-PEGMA synthesized in step (1) into a 100ml round bottom flask 526 , 0.203g 2-bromoisobutyric acid monomethoxyethylene glycol ester, 0.237g 4,4'-dinonyl-2,2'-bip...
Embodiment 2
[0060] Synthesis of water-dispersible cross-linkable fluoropolymer by anionic polymerization, comprising the following steps:
[0061] (1) Synthesis of monomer Epoxy-PEGA 300
[0062] Add 4.5% polyethylene glycol acrylate (Mn=300) and 22ml epichlorohydrin to cyclohexanone, then add catalyst tetrabutylammonium fluoride and potassium hydroxide, react at 50°C for 20 hours, and wash , Precipitate to obtain polyethylene glycol acrylate with epoxy group at the end (ie Epoxy-PEGA 300 ); wherein the mass ratio of polyethylene glycol methyl acrylate, epichlorohydrin, cyclohexanone, tetrabutylammonium fluoride and potassium hydroxide is 1:10:100:1:1.
[0063] The above process takes place as follows:
[0064]
[0065] (2) Synthesis of water-dispersible cross-linkable fluoropolymer
[0066] 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-butyllith...
Embodiment 3
[0070] Synthesis of water-dispersible cross-linkable fluoropolymer by "Click" method, including the following steps:
[0071] (1) Synthesis of monomer Epoxy-PEGMA 526
[0072] Same as step (1) of Example 1.
[0073] (2) Synthesis of water-dispersible cross-linkable fluoropolymer
[0074] Add 2.852g of monomer Epoxy-PEGMA synthesized in step (1) into a 100ml round bottom flask 526 , 0.103g trimethylsilyl ATRP initiator, 0.237g 4,4'-dinonyl-2,2'-bipyridine and 3ml anisole, stir and dissolve the reaction system, bubble with argon for 30min, and remove Oxygen, then transfer the reaction system to a 100ml round bottom flask containing 0.1124g cuprous bromide, carry out polymerization reaction at 40°C for 2h, the reaction product is precipitated in methanol, washed with methanol and then washed with n-hexane, then at room temperature Under vacuum drying for 24h to constant weight, the product end is P(Epoxy-PEGMA 526 ).
[0075] In a 100ml round-bottomed flask, add 0.15g of th...
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