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Ring-opening polymerization of propylene oxide by double metal cyanide catalysts prepared by reacting CoCl2 with various metal cyanide salts

2013; Elsevier BV; Volume: 232; Linguagem: Inglês

10.1016/j.cattod.2013.09.038

1873-4308

Seong Jae Yu, Yinshan Liu, Seong Jin Byeon, Dae Won Park, Il Kim,

biodegradable polymer synthesis and properties

Polymerization of propylene oxide (PO) has been carried out by using a series of double metal cyanide (DMC) catalysts prepared by reacting dicationic CoCl2 with dianionic K2Ni(CN)4, K4Fe(CN)6, trianionic K3Fe(CN)6, or K3Co(CN)6 in the presence of tert-butyl alcohol as the complexing agent and poly(tetramethylene ether) glycol as the co-complexing agent. The resulting DMC catalysts are characterized by elemental analysis, X-ray photoelectron spectroscopy, infrared spectroscopy, and X-ray diffractometry. Screening the catalytic activity in PO polymerization shows that it is dependent on the type of catalyst, relative ratio of cationic cobalt and anionic metal salts, and polymerization conditions. Thus, the DMC catalyst prepared by reacting CoCl2 with K2Ni(CN)4 yielded the highest activity. The polyols produced by DMC catalysts had a very low level of unsaturation. The molecular weight and particularly the polydispersity of the resulting polyols are sensitive to the type of anionic metal salts.