Method for preparing irregular sulfonated poly aromatic (sulfur) ether with high efficiency
A sulfonated poly and aromatic technology, which is applied in the field of efficient preparation of novel random sulfonated polyaromatic ethers, can solve the problems of complicated recovery process, large volume of reaction solution, long reaction time, etc., and achieves simplified equipment composition and simplified process. , the effect of high molecular weight
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Embodiment 1
[0053] according to figure 2 In the shown reaction device, 3,3'-sodium disulfonate-4,4'-dichlorodiphenylsulfone (SDCDPS, 17.1938g, 35mmol), 4,4'-dichlorodiphenylsulfone (DCDPS, 18.6654 g, 65mmol), 4,4'-biphenol (BP, 18.6210g, 100mmol), anhydrous potassium carbonate (K 2 CO 3 , 27.6420g, 200mmol), 272mL N,N-dimethylacetamide (DMAc) were mixed, the reaction temperature was raised to 180°C, and the reaction was carried out for 12 hours. Stop heating and stirring, and cool to room temperature naturally. The reaction solution was slowly poured into 2L of deionized water to obtain a white fibrous polymer, soaked in 4L of deionized water for 8 hours at 80°C, repeated three times, filtered, dried, and then vacuum-dried at 100°C for 24 hours to obtain a shallow Yellow fibrous polymer (sulfonated polyethersulfone compound), 46.7 g, yield: 99%, intrinsic viscosity: 0.91 dL / g.
Embodiment 2
[0055] according to figure 2 In the shown reaction device, 3,3'-sodium disulfonate-4,4'-dichlorodiphenylsulfone (SDCDPS, 17.1938g, 35mmol), 4,4'-dichlorodiphenylsulfone (DCDPS, 18.6654 g, 65mmol), 4,4'-biphenol (BP, 18.6210g, 100mmol), anhydrous potassium carbonate (K 2 C0 3 , 27.6420g, 200mmol), 272mL of N-methylpyrrolidone (NMP) were mixed, the reaction temperature was raised to 190°C, and the reaction was carried out for 12 hours. Stop heating and stirring, and cool to room temperature naturally. The reaction solution was slowly poured into 2L of deionized water to obtain a light yellow fibrous polymer, soaked in 4L of deionized water at 80°C for 8 hours, repeated three times, filtered, dried, and then vacuum-dried at 100°C for 24 hours to obtain Yellow fibrous polymer (sulfonated polyethersulfone compound), 44.3 g, yield: 94%, intrinsic viscosity: 0.89 dL / g.
Embodiment 3
[0057] according to figure 2 In the shown reaction device, 3,3'-sodium disulfonate-4,4'-dichlorodiphenylsulfone (SDCDPS, 17.1938g, 35mmol), 4,4'-dichlorodiphenylsulfone (DCDPS, 18.6654 g, 65mmol), 4,4'-biphenol (BP, 18.6210g, 100mmol), anhydrous potassium carbonate (K 2 CO 3 , 27.6420g, 200mmol), 272mL N,N-dimethylacetamide (DMAc) were mixed, the reaction temperature was raised to 180°C, and the reaction was carried out for 24 hours. Stop heating and stirring, and cool to room temperature naturally. The reaction solution was slowly poured into 2L of deionized water to obtain a white fibrous polymer, soaked in 4L of deionized water for 8 hours at 80°C, repeated three times, filtered, dried, and then vacuum-dried at 100°C for 24 hours to obtain a shallow Yellow fibrous polymer (sulfonated polyethersulfone compound), 46.7 g, yield: 99%, intrinsic viscosity: 1.04 dL / g.
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