1998
DOI: 10.1007/bf02475256
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Catalytic utilization of carbon dioxide to polymer blends via cyclic carbonate

Abstract: In the present study, the synthesis of bis(cyclic carbonate) fTom carbon dioxide and bisphenol A ( or bisphenol S )-diglycidyl ether was investigated using quaternary ammonium salts as catalyst. Among the salts tested, the one having a larger alkyl group and more nucleophflic counter anion exhibited a better catalytic activity. Poly(hydmxyurethane)s were prepared by the polyaddition reaction of bis(cyclic carbonate) and diamine. The poly(hydroxyurethane) has shown higher thermal stability than conventional pol… Show more

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Cited by 5 publications
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“…The mixture was stirred at room temperature for 2 h. After that, the acetone was removed by rotary evaporator, and the rest part was extracted by acetic ether. After dried, the cru Synthesis of the Polymers sPAR: Polycondensation was carried out in an aqueous/organic two phase system, using tetrabutyl ammonium bromide as the phase transfer catalyst [17][18][19]. Isophthaloyl dichloride (4.06 g, 20 mmol) in 50 mL of dichloroethane was added to 5.72 g (20 mmol) of diphenolicacid in 100 ml of aqueous NaOH solution (including 30 mmol NaOH) in the presence of 0.1 g of tetrabutyl ammonium bromide.…”
Section: Synthesis Of the Chromophoresmentioning
confidence: 99%
“…The mixture was stirred at room temperature for 2 h. After that, the acetone was removed by rotary evaporator, and the rest part was extracted by acetic ether. After dried, the cru Synthesis of the Polymers sPAR: Polycondensation was carried out in an aqueous/organic two phase system, using tetrabutyl ammonium bromide as the phase transfer catalyst [17][18][19]. Isophthaloyl dichloride (4.06 g, 20 mmol) in 50 mL of dichloroethane was added to 5.72 g (20 mmol) of diphenolicacid in 100 ml of aqueous NaOH solution (including 30 mmol NaOH) in the presence of 0.1 g of tetrabutyl ammonium bromide.…”
Section: Synthesis Of the Chromophoresmentioning
confidence: 99%