A kind of active hydroxyl-containing polyarylether and its preparation method and application
A technology of hydroxypolyarylether and methoxypolyarylether, which is applied in the field of polymer synthesis, can solve the problem of low glass transition temperature or melting point, difficult application of high temperature, high corrosion resistance, heat resistance, mechanical properties and corrosion resistance Poor stability and other problems, to achieve the effect of high molecular weight, strong repeatability and good stability
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[0056] The invention provides a polyarylether containing active hydroxyl and its preparation method, which is characterized in that a class of diphenol containing both hydroxyl and methoxy is firstly designed and synthesized, and then it is subjected to nucleophilic substitution with a dihalogenated aromatic monomer A polyarylether resin containing methoxy groups in the molecular chain is prepared by polycondensation, and then a polyarylether resin containing active hydroxyl groups in the molecular chain of the polymer is obtained through a demethoxyl hydroxylation reaction. It not only reasonably introduces the active hydroxyl group into the polymer structure, but also maintains the excellent thermal properties, mechanical properties and processability of the resin; through further modification of the hydroxyl group, a series of functional polymer materials can be prepared. The development of high-performance functional polymer materials has laid a solid foundation.
[0057] ...
Embodiment 1
[0064] (1) Preparation of methoxy cyclohexyl diphenol monomer:
[0065] Add 98g of cyclohexanone, 248g of guaiacol, 1g of thioglycolic acid, and 500g of 80% sulfuric acid into a three-necked flask with a stirrer, a thermometer and a reflux condenser in sequence, react at a temperature of 20°C for 36h under nitrogen protection, and precipitate solid; pour the above-mentioned solid-containing reaction solution into cold water, filter, collect the filter cake, wash the filter cake with deionized water to remove water-soluble impurities, and rinse with dichloromethane to further remove impurities, and vacuum dry to obtain purified Containing methoxycyclohexyl diphenol monomer, after drying, 234.6g of purified methoxycyclohexyl diphenol monomer was obtained, with a yield of about 69%. For details of IR and NMR characterization, see figure 1 , image 3 shown;
[0066] (2) Preparation of active methoxy polyarylether
[0067] 28.7g of 4,4'-dichlorodiphenylsulfone, 10g of sodium ace...
Embodiment 2
[0073] (1) Preparation of methoxy cyclohexyl diphenol monomer
[0074] Add 98g of cyclohexanone, 720g of guaiacol, 8g of mercaptophenylacetic acid, 1500g of glacial acetic acid: hydrochloric acid (3:1) into a three-necked flask with a stirrer, a thermometer and a reflux condenser in sequence. React for 2 hours under the protection of nitrogen, and the solid is precipitated; pour the above-mentioned solid-containing reaction solution into cold water, filter, collect the filter cake, wash the filter cake with deionized water to remove water-soluble impurities, and rinse with dichloromethane to further remove impurities , vacuum drying to obtain purified methoxycyclohexyl-diphenol-containing monomer, and after drying, 244.8 g of purified methoxycyclohexyl-diphenol-containing monomer was obtained, with a yield of about 72%. For details of infrared and NMR characterization, see figure 1 , image 3 shown;
[0075] (2) Preparation of active methoxy polyarylether
[0076] 21.8g of ...
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