Process for synthesizing electron conductive polymer poly-o-amino-thiophenol
A technology of o-aminothiophenol and its synthesis method, which is applied in the field of synthesis of electronically conductive polymer poly-o-aminothiophenol, can solve the problems of high emulsifier concentration, high preparation cost, and difficult removal, and reduce the degree of oxidation , increase the molecular weight, reduce the effect of oxidation degree
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Embodiment 1
[0020] Under nitrogen protection, 80mL 0.12mol / L HCl and 3.802g SDS (0.12mol / L) were successively added to a 250mL reactor, heated to 70°C, and after the dissolution was complete, 1.252g o-aminothiophenol (0.1 mol / L), stir evenly, and dissolve 0.014mol APS in 30mL 0.12mol / L HCl solution, slowly drop into the reaction system, about 1.0h to complete the drop. After reacting for 10 hours, the reaction solution was left standing in a refrigerator at 6° C. for 24 hours, and 70 mL of ethanol was added to break the emulsification and precipitate the polymer. Suction filtration, wash the solid with deionized water until the filtrate has no foam, and then wash with ethanol several times until the filtrate is colorless, and vacuum-dry at room temperature to obtain brown powdery polymer PAT (HCl), with a yield of about 85%.
Embodiment 2
[0022] Under nitrogen protection, 50mL 0.2mol / L HCl and 2.88g SDS (0.1mol / L) were successively added to a 250mL reactor, heated to 50°C, and after the dissolution was complete, 0.626g o-aminothiophenol ( 0.05mol / L), stir evenly, and dissolve 0.01mol APS in 50mL 0.1mol / L HCl solution, slowly drop into the reaction system, about 2.0h to finish. After reacting for 12 hours, the reaction solution was placed in a refrigerator at 5° C. for 24 hours, and 60 mL of ethanol was added to break the emulsification and precipitate the polymer. Suction filtration, wash the solid with deionized water until the filtrate has no foam, and then wash with ethanol several times until the filtrate is colorless, and vacuum-dry at room temperature to obtain brown powdery polymer PAT (HCl), with a yield of about 75%.
Embodiment 3
[0024] Under the protection of argon, add 100mL of 0.3mol / L HCl and 8.064g of SDS (0.2mol / L) to a 250mL three-necked flask successively, heat to 80°C, and after the dissolution is complete, add 2.5014g of anthranilic acid dropwise Phenol (0.2mol / L), stir evenly, and dissolve 0.03mol APS in 40mL 0.2mol / L HCl solution, slowly drop into the reaction system, about 1.5h to finish. After reacting for 8 hours, the reaction solution was placed in a refrigerator at 8° C. for 24 hours, and 100 mL of ethanol was added to break the emulsification and precipitate the polymer. Suction filtration, wash the solid with deionized water until the filtrate has no foam, and then wash with ethanol several times until the filtrate is colorless, and vacuum-dry at room temperature to obtain brown powdery polymer PAT (HCl), with a yield of about 60%.
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