Organic zinc catalyst, and process for production of poly(alkylene carbonate) using the same
A polyalkylene carbonate and catalyst technology, applied in the field of organic zinc catalysts, can solve the problems of low polymerization activity, high risk and high price, and achieve the effects of easy separation, high reaction efficiency and high polymerization activity
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Embodiment 1
[0062]
[0063] 8.1 g (100 mmol) of zinc oxide, 12.7 g (96 mmol) of glutaric acid, 0.1 g (2 mmol) of acetic acid and 150 mL of toluene were placed in a 300 mL capacity four-necked flask equipped with a cooling tube, a thermometer and a stirrer. Then, it heated up to 55 degreeC under nitrogen atmosphere, and stirred at this temperature for 4 hours, and made it react. Then, the temperature was raised to 110° C., and stirred at this temperature for 4 hours to make it azeotrope, and after removing moisture, it was cooled to room temperature to obtain a reaction solution containing the organozinc catalyst of the present invention. A part of this reaction solution was fractionated, and the organozinc catalyst of the present invention obtained by filtering it was subjected to IR measurement (Thermo Nicolet Japan Co., trade name AVATAR360). As a result, no peak due to carboxylic acid groups was observed.
[0064]
[0065] In a 1L autoclave equipped with a thermometer and a stirrer...
Embodiment 2
[0069] In the manufacture of polyalkylene carbonate in Example 1, except that 46.4 g (0.80 mol) of propylene oxide was used instead of 35.2 g (0.80 mol) of ethylene oxide, polytrimethylene carbonate 80.8 was obtained in the same manner as in Example 1. g.
[0070] The obtained polypropylene carbonate can be identified because it has the following physical properties.
[0071] IR (KBr): 1742, 1456, 1381, 1229, 1069, 787 (cm -1 )
Embodiment 3
[0073]
[0074] 8.1 g (100 mmol) of zinc oxide, 12.7 g (96 mmol) of glutaric acid, and 150 mL of toluene were placed in a 300 mL capacity four-necked flask equipped with a cooling tube, a thermometer, and a stirrer. Then, the temperature was raised to 55° C. under a nitrogen atmosphere, and the mixture was stirred at this temperature for 2 hours to allow a reaction. Then, 0.1 g (2 mmol) of acetic acid was further added, and stirred at this temperature for 2 hours to make it react. Then, the temperature was raised to 110° C., and stirred at this temperature for 4 hours to make it azeotrope, and after removing moisture, it was cooled to room temperature to obtain a reaction solution containing the organozinc catalyst of the present invention. A part of this reaction solution was fractionated, and the organozinc catalyst of the present invention obtained by filtering it was subjected to IR measurement (Thermo Nicolet Japan Co., trade name AVATAR360). As a result, no peak due to...
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