Process for preparing perfluorosulfonyl resin
A technology of perfluorosulfonyl vinyl ether and perfluoroalkane, which is applied in the field of preparing perfluorosulfonyl resins, can solve problems affecting conversion rate, difficulty in handling, cost impact, etc., so as to improve conversion rate and yield and improve reliability regulatory effect
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Embodiment 1
[0047] Add 600g perfluorosulfonyl vinyl ether (PSVE) (commercial grade) and 0.06g isopropyl peroxydicarbonate (50% CFC-113 solution) into a 2L stainless steel reactor at room temperature, then add 1000g C 7 f 16 / C 8 f 16 o 2 mixture as a solvent (wherein C 8 f 16 o 2 for 300g). Replace with nitrogen and then replace with TFE, then pass through TFE to pressurize, raise the temperature to 70°C, adjust the pressure to keep the pressure of TFE at 1200kPa, react for 2 hours, cool down, and discharge the material. 10 kg of chloroform was added with stirring, and the precipitated white product was centrifuged, washed with water, and dried in a vacuum environment at 100° C. to obtain a translucent powder. The solution after centrifugation is subjected to fractional distillation to recover chloroform, polymerization solvent and unreacted monomer.
Embodiment 2
[0049] The process described in Example 1 was repeated, except that disuccinic acid peroxide was used as the initiator. As a result, the F content of the product obtained was 68.7%, the EW value was 888g / mol, the melting temperature was 201°C, and the thermal decomposition temperature was 360°C. ℃.
Embodiment 3-5
[0051] The process described in Example 1 was repeated, except that the polymerization time was respectively 3 hours, 5 hours, and 8 hours. The analytical test results of Examples 1 and 3 to 5 are listed in Table 1.
[0052]
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