Antifouling coating material and preparation method thereof
An anti-fouling coating and initiator technology, applied in the field of materials, can solve the problems of algae and fish threats, toxicity, etc., and achieve the effects of inhibiting adhesion, enhancing anti-fouling performance, and enhancing surface wetting resistance
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[0022] The invention provides a method for preparing an antifouling coating material, comprising:
[0023] A) thermoplastic styrene-butadiene block copolymer, dodecafluoroheptyl methacrylate and initiator are mixed and reacted to obtain a reaction product;
[0024] B) mixing the reaction product with mesoporous molecular sieves to obtain an antifouling coating material.
[0025] In the invention, firstly, the thermoplastic styrene-butadiene block copolymer is dissolved in a solvent, mixed with dodecafluoroheptyl methacrylate (DFHMA) and an initiator, and reacted to obtain a reaction product; the reaction product is settled with a sedimentation agent. The steps A1) and A2) preferably further include: adding the reaction product to an initiator to continue the reaction.
[0026] The present invention first dissolves the thermoplastic styrene-butadiene block copolymer with a solvent, mixes it with dodecafluoroheptyl methacrylate and an initiator, and reacts to obtain a reaction ...
Embodiment 1
[0045] Add 2g of P123 to the mixture of 2mol / L 60g of HCl and 15g of distilled water, stir magnetically at room temperature until P123 is completely dissolved and the solution is clear and transparent, then add 4.25g of TEOS dropwise to the above solution under strong stirring, and continue at room temperature Stir for 20 h, transfer the reaction mixture to a polytetrafluoroethylene-lined hydrothermal kettle, place it at 100°C for aging for 24 h, cool at room temperature, filter with suction, wash with deionized water, and dry to a white solid. The solid was transferred to a resistance furnace, and the temperature was programmed to rise (2°C / min) to 550°C for 5 hours to obtain 1.06g of SBA-15 powder sieve.
Embodiment 2
[0051] Add 1g of SBS (number-average molecular weight: 100,000) into 10g of tetrahydrofuran, stir magnetically for 0.5h to dissolve, add 1g of DFHMA and 0.015g of azobisisobutyronitrile, stir magnetically at 65°C, turn off the heat source after reacting for 5 hours, and then add Add 0.005 g of azobisisobutyronitrile and react at room temperature for 24 hours. After the reaction was finished, the reactants were settled with 15 g of ethanol, and the dissolution and sedimentation were repeated twice to remove residual initiators and reaction by-products. The product was dried in a vacuum oven at 50°C until constant weight, and stored for later use.
[0052] Dissolve 1 g of the above-prepared fluorinated copolymer into 10 g of tetrahydrofuran, dissolve it under magnetic stirring, add 0.1 g of SBA-15 molecular sieve prepared in Example 1 of the present invention, and stir thoroughly. Apply it evenly on a clean tinplate sheet with a thickness of 60 μm, and dry at 60°C for 3 hours t...
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