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Effect of dicarbonyl complexing agents on double metal cyanide catalysts toward copolymerization of CO2 and propylene oxide

Authors
Tran, Chinh HoangKim, Sun AMoon, YejiLee, YechanRyu, Hyun MoBaik, Joon HyunHong, Sung ChulKim, Il
Issue Date
Sep-2021
Publisher
Elsevier B.V.
Keywords
Carbon dioxide; Complexing agents; Copolymerization; Double metal cyanide; Heterogeneous catalysis; Polycarbonate; Polyol; Propylene oxide
Citation
Catalysis Today, v.375, pp 335 - 342
Pages
8
Journal Title
Catalysis Today
Volume
375
Start Page
335
End Page
342
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/146869
DOI
10.1016/j.cattod.2020.01.008
ISSN
0920-5861
1873-4308
Abstract
Functional polycarbonate polyols have been synthesized by COFunctional polycarbonate polyols have been synthesized by CO2/propylene oxide (PO) copolymerizations using various Zn(II)-Co(III) double metal cyanide (DMC) catalysts bearing alpha-, 13-, gamma-, and delta-dicarbonyl complexing agents (CAs) including dicarboxylic acids, diesters, ketoester, and diketones. The resultant heterogeneous catalysts are intensively characterized by infrared, absorption and X-ray photoelectron spectroscopies, X-ray powder diffraction, and elemental analysis. The produced polycarbonate polyols are characterized using infrared and nuclear magnetic resonance spectroscopies, gel permeation chromatography, differential scanning calorimetry and thermogravimetric analysis measurements. The catalysts bearing 13-, gamma-, and delta-dicarbonyl CAs exhibit high activity towards CO2/PO copolymerization and produce polycarbonate polyols with high carbonate content, wide range of molecular weight and narrow polydispersity. The functionality of the resultant polycarbonate polyols varies depending on the type of CAs and the functionality of initiators.
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