Polyisophthaloyl metaphenylene diamine fiber and preparation method thereof
A technology of polym-phenylene isophthalamide and isophthaloyl chloride, which is applied in the direction of single-component polyamide rayon, fiber treatment, spinning solution preparation, etc., and can solve the problem of polyisophthalamide The m-phenylenediamine fiber has low strength, grooves are easy to appear on the surface of the fiber, and the performance of aramid fiber is restricted. It is beneficial to fiber dyeing, high in strength and toughness, and compact in structure.
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Embodiment 1
[0026] Add 0.3mol of m-phenylenediamine with a purity of 99% to 300ml of amide polar organic solvent N,N-dimethylacetamide (DMAc) with a purity of more than 99%; stir for 10 minutes to dissolve completely, and then Cool to -10°C in a cooling bath, add isophthaloyl chloride in an equimolar ratio to m-phenylenediamine twice within 5 minutes into the mixed solution formed by m-phenylenediamine and amides polar organic solvents, and then Remove the cooling bath and carry out the polymerization reaction for 60 minutes, then add calcium hydroxide in an equimolar ratio to m-phenylenediamine into the mixed liquid within 10 minutes, neutralize the by-product hydrochloric acid generated by the polymerization reaction to generate hydrogen chloride, and obtain poly-m-phenylene Diformyl m-phenylenediamine spinning stock solution, at this time, the polymer concentration measured in the spinning stock solution is 23wt%, the inherent viscosity is 5.1dl / s, and the whole polycondensation reactio...
Embodiment 2
[0031] Add 0.3mol of m-phenylenediamine with a purity of 99% to 300ml of amide polar organic solvent N,N-dimethylacetamide (DMAc) with a purity of more than 99%; stir for 15 minutes to dissolve completely, then Cool to -5°C in a cooling bath, add isophthaloyl chloride in an equimolar ratio to m-phenylenediamine twice within 8 minutes to the mixed solution formed by m-phenylenediamine and amides polar organic solvents, and then Remove the cooling bath and carry out the polymerization reaction for 50 minutes, then add calcium hydroxide in an equimolar ratio to m-phenylenediamine into the mixed liquid within 10 minutes, neutralize the by-product hydrochloric acid generated by the polymerization reaction to generate hydrogen chloride, and obtain poly-m-phenylene Diformyl m-phenylenediamine spinning stock solution, at this time, the polymer concentration measured in the spinning stock solution is 21wt%, the inherent viscosity is 5.5dl / s, and the whole polycondensation reaction is ca...
Embodiment 3
[0036] Add 0.3 mol of m-phenylenediamine with a purity of 99% to 300ml of amide polar organic solvent N-methyl-2-pyrrolidone (NMP) with a purity of more than 99%; stir for 20 minutes to dissolve completely, then cool Cool in the bath to -12°C, add isophthaloyl chloride in an equimolar ratio to m-phenylenediamine into the mixed solution formed by m-phenylenediamine and amide polar organic solvent twice within 10 minutes, and then remove After cooling the bath for 40 minutes of polymerization reaction, calcium hydroxide with an equimolar ratio of m-phenylenediamine was added to the mixed solution within 10 minutes to neutralize the by-product hydrochloric acid generated by the polymerization reaction to generate hydrogen chloride to obtain poly-m-phenylenediamine Formamide m-phenylenediamine spinning stock solution, at this time, the polymer concentration measured in the spinning stock solution is 19wt%, the inherent viscosity is 5.0dl / s, and the whole polycondensation reaction i...
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