In-situ polymerization type N-P synergistic flame-retardant nylon and preparation method thereof
A synergistic flame-retardant and polymeric technology, applied in the field of in-situ polymerized N-P synergistic flame-retardant nylon and its preparation
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[0069] The preparation method of in-situ polymerized N-P synergistic flame-retardant nylon of the present invention specifically comprises the following steps:
[0070] (A) Reaction of organophosphorus flame retardant monomers with diamines, preferably with excess amino groups, to form salts;
[0071] (B) make the reaction product of step (A) and diacid and diamine or dibasic amide salt in the presence of 1-10wt% relative to the total weight of all polymerized monomers, preferably 3-6wt% nitrogen-based flame retardant The following reaction is used to prepare in-situ polymerized N-P synergistic flame-retardant nylon.
[0072] In step (A), preferably, the diamine monomer is slightly excessive, so that the pH of the salt solution is 7-9. The reaction temperature rose from room temperature to 40-70°C within 5-20 minutes.
[0073] Preferably, the diamine monomers described in step (A) are hexamethylenediamine, decanediamine, nonanediamine, undecanediamine, dodecanediamine, aliph...
Embodiment 1
[0089] Stir the flame retardant monomer and hexamethylenediamine in an aqueous solution at 40°C for 0.5h at a molar ratio of 1:1.2, adjust the pH of the solution to 7.2, and obtain a salt solution.
[0090] High-speed shear emulsification of 4% MCA accounting for the total mass of polymerized monomers (including the above-mentioned salt solution and the following nylon 66 salt) in a certain amount of water for 10 minutes to obtain a uniformly dispersed MCA emulsion.
[0091] Mix the nylon 66 salt (hexamethylene adipamide salt) solution with the salt solution obtained above, the MCA emulsion, and the catalyst hypophosphorous acid each accounting for 1‰ Add sodium, antioxidant p-phenylenediamine, and 40% deionized water to the reactor, vacuumize it, and fill it with nitrogen for 5 times, and finally keep the internal pressure of the reactor at 0.2MPa. Heat the reactor, keep stirring at a high speed, and when the temperature of the reactor reaches 220°C and the pressure is 1.8 MP...
Embodiment 2
[0094] Stir and react the flame retardant monomer and hexamethylenediamine in an aqueous solution at a molar ratio of 1:1.3 at 50°C for 1 hour, and adjust the pH of the solution to 7.8.
[0095] 3% MCA accounting for the total mass of polymerized monomers was emulsified in a certain amount of water at high speed for 6 minutes to obtain a uniformly dispersed MCA emulsion.
[0096] Adipic acid and hexamethylenediamine are configured according to a mass ratio of 1:1.3, and the above-mentioned salt solution, MCA emulsion, catalyst toluenesulfonic acid and antioxidant Agent 2, 6-di-tert-butyl-4-methylphenol, and 35% deionized water were added to the reactor, vacuumed and filled with nitrogen for 3 times, and finally the internal pressure of the reactor was kept at 0.3 MPa. Heat the reactor, keep stirring at a high speed, and when the temperature of the reactor reaches 215°C and the pressure is 1.7 MPa, keep the temperature and pressure constant for 1.6 hours. Then the temperature ...
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