Method for depolymerising oxygenated polymer materials by nucleophilic catalysis
A polymer and compound technology, applied to aliphatic compounds in the construction industry, petrochemical industry, electrical fields, can solve the problems of several types of recycling, and achieve the effect of large industrial value and low price
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Embodiment 1
[0267]Example 1 : Trimethoxysilane ((MEO)3SiH) and Kotbu to solve PC-BPA
[0268]
[0269]The commercially available PC-BPA (123.2 mg; 0.5 mmol; 1 mole) and trimethoxysilane (244 mg; 2 mmol; 4 molar equivalents) were added to 1.5 ml of THF. The KOTBU catalyst (0.05 molar equivalents) was added while stirring. The reaction was reacted at room temperature (20 ° C ± 5 ° C), and then the solvent was evaporated under vacuum. The resulting product IIA was purified by using the same conditions described in the general method of operation. By purification, a product IIa having very high purity is obtained, wherein the yield is 97% relative to the introduced starting material.
[0270]At 25 ° C, 10 mL of NaOH (10%) in the methanol / water mixture was directly added to the reaction mixture, and a hydroxy product of a 2-hour product IIa was performed. The hydrolyzate (BPA) of the white solid was obtained by purification by the column using the condition described in the general operation method.
Embodiment 2
[0271]Example 2 : Trimethoxysilane ((MEO)3SiH)) and TBAT to explain PC-BPA
[0272]
[0273]Using (MEO)3SiH and KOTBUs to explain the same manner as in Example 1 of PC-BPA, and to deliver with TBAT (0.05 molar equivalents). In this case, 123.2 mg of PC-BPA (0.5 mmol; 1 molar equivalents) with 244 mg of trimethoxysilane (244 mg; 2 mmol; 4 molar equivalents) and 0.05 molar equivalent TBAT (13.5 mg, 0.025 mmol, 5 mol%) is used together. After 6 hours, it was completely converted into IIA. The product was purified by the same method of operation as in Example 1.
[0274]The hydrolysis of the product IIa made BPA (white solid, yield of 92%).
Embodiment 3
[0275]Example 3 : Trimethoxysilane ((MEO)3SiH) and TBAF (1M in THF) to solve PC-BPA
[0276]
[0277]Using (MEO)3SiH and KOTBUs to explain the same manner as in Example 1 of PC-BPA, and the TBAF (1M in THF) is given. In this case, 123.2 mg of PC-BPA (0.5 mmol; 1 molar equivalents) was used to trimethoxysilane (244 mg; 2 mmol; 4 molar equivalents) and 50 μl of TBAT (0.05 mmol, 0.1 molar equivalents). After 12 hours, it was completely converted into IIA.
[0278]The product was purified by the same method of operation as in Example 1. The hydrolysis of the product IIa made BPA (white solid, yield of 92%).
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