Process for the production of branched melt polycarbonate by late addition of fries-inducing catalyst
A technology of polycarbonate and catalyst, applied in the field of branched polycarbonate composition, can solve problems such as high cost
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Embodiment 1
[0085] Example 1: A batch reactor tube was charged with 50 grams of polycarbonate A and 2.5 x 10 -6 moles of NaOH (relative to 1 mole of bisphenol acetone). The mixture was heated to a temperature of 310°C and stirred for 20 minutes. After the melt mixing stage, vacuum was applied to the system to a pressure of 0.5 mbar and the reaction was continued for 30 minutes. After 30 minutes, the pressure was increased to atmospheric pressure and 13.5 ppm butyl tosylate (relative to polymer material) was added to the melt and stirred for an additional 5 minutes. After the reaction, the polymer was sampled from the reaction tube. As summarized in Table 2, the MIR increased from 1.1 to 2.0.
Embodiment 2
[0086] Example 2: A batch reactor tube was charged with 50 grams of polycarbonate A and 7.5 x 10 -6 moles of NaOH (relative to 1 mole of bisphenol acetone). The mixture was heated to a temperature of 310°C and stirred for 20 minutes. After the melt mixing stage, vacuum was applied to the system to a pressure of 0.5 mbar and the reaction was continued for 30 minutes. After 30 minutes, the pressure was increased to atmospheric pressure and 40.5 ppm butyl tosylate (relative to polymer material) was added to the melt and stirred for an additional 5 minutes. After the reaction, the polymer was sampled from the reaction tube. As summarized in Table 2, the MIR increased from 1.1 to 3.7.
Embodiment 3
[0087] Embodiment 3: repeat embodiment 2, but do not use sodium hydroxide, will 7.5 * 10 -6 A mole of disodium sebacate (D) (relative to 1 mole of bisphenolacetone) was added to the polymer. As summarized in Table 2, the MIR increased from 1.1 to 2.8.
[0088]
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