A modified meta-aramid fiber, its preparation method and hollow fiber membrane
A fiber membrane and aramid fiber technology, which is applied in the directions of fiber processing, fiber chemical characteristics, hollow filament manufacturing, etc., can solve the problems of difficult dry storage, high intrinsic viscosity, and poor chlorine resistance of membrane fibers, and achieve good film formation. high performance, simple preparation process and good hydrophilicity
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Embodiment 1
[0056] Add 42.45 mL of DMAc solvent, 0.077 mol of m-phenylenediamine, 0.0385 mol of ethylenediamine and 0.0385 mol of 4-fluoro-1,3-phenylenediamine into a four-necked flask, and stir to dissolve. Adjust the reaction temperature to -25°C, add 0.1155mol of isophthaloyl chloride, control the reaction temperature of the reaction system below 0°C, and continue to add 0.0262mol of isophthaloyl chloride until the viscosity of the system is stable. After the viscosity is stable, finally add 0.0123mol of isophthaloyl chloride, control the reaction temperature below 60°C until the reaction is complete, add 0.154mol of calcium hydroxide and continue to stir until the neutralization is complete (pH value = 7). At this time, the content of the modified meta-aramid polymer in the solution was 42 wt%. Take out a small part of the solution and dilute it with deionized water to obtain the modified meta-aramid polymer, and continue to wash it three times with deionized water. After the polymer ...
Embodiment 2
[0058] Under nitrogen protection, add 68.9mL of DMAc solvent, 0.077mol of m-phenylenediamine, 0.0385mol of hexamethylenediamine and 0.0385mol of 4-chloro-1,3-phenylenediamine into a 1L four-necked flask equipped with mechanical stirring and a thermometer , stirred under nitrogen protection at room temperature until the solute was completely dissolved. Adjust the reaction temperature to -25°C with a freezing bath, add 0.1155mol of isophthaloyl chloride under stirring, control the reaction temperature of the reaction system to be lower than 0°C, and continue to add 0.0262mol of isophthaloyl dimethanol after reacting until the viscosity of the system is stable Acyl chloride, after the reaction until the viscosity of the system is stable, add 0.0123mol isophthaloyl chloride at the end, the solution starts to thicken, the temperature rises, adjust the stirring speed and control the reaction temperature below 60°C until the reaction is complete, add 0.154mol calcium hydroxide Then c...
Embodiment 3
[0060] Under nitrogen protection, add 66.21mL of DMAc solvent, 0.077mol of m-phenylenediamine, 0.0385mol of dodecanediamine and 0.0385mol of 5-trifluoromethyl-1,3-phenylenediamine into the In a 1L four-neck flask, stir under nitrogen protection at room temperature until the solute is completely dissolved. Adjust the reaction temperature to -25°C with a freezing bath, add 0.1155mol of isophthaloyl chloride under stirring, control the reaction temperature of the reaction system to be lower than 0°C, and continue to add 0.0262mol of isophthaloyl dimethanol after reacting until the viscosity of the system is stable Acyl chloride, after the reaction until the viscosity of the system is stable, add 0.0123mol isophthaloyl chloride at the end, the solution starts to thicken, the temperature rises, adjust the stirring speed and control the reaction temperature below 60°C until the reaction is complete, add 0.154mol calcium hydroxide Then continue to stir until neutralization is complet...
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