Synthesis of Double Alkyl EO/PO Random Copolyethers with KOH Catalyst

2012 ◽  
Vol 472-475 ◽  
pp. 2681-2685
Author(s):  
Jian Guo Guo ◽  
Su Qin He ◽  
Jian Ming Jiang

Ethylene oxide (EO) and propylene oxide (PO) random copolymer was synthesized with 1,2-propanediol as initiator, then the end-capping process was carried out by adding various alkyl halides and potassium hydroxide (KOH) to produce the double alkyl EO/PO random copolyethers. The factors effecting alkyl-capping rate were discussed. The results showed that when the molar ratio of hydroxyl group/KOH/1-bromobutane was 1/1.9/1.9, reacting time 6.5 hr and reacting temperature 50°C, the alkyl-capping rate could reach over 80%. The end-capping rate would also increase with the increasing content of ethylene oxide in the random polyether, and the end-capping rate of the EO/PO/EO block-polyether was high than that of the random polyether with same molecular weight. Instead of 1-bromobutane, ethyl bromide promised a higher whereas chloralkane gave a lower end-capping rate respectively.

2003 ◽  
Vol 22 (1) ◽  
pp. 23-42 ◽  
Author(s):  
Wu Suen ◽  
Jennifer Percy ◽  
Shaw L. Hsu ◽  
Igor A. Kaltashov ◽  
Howard D. Stidham

Matrix Assisted Laser Desorption Ionization Time-of-Flight mass spectrometry has been applied to obtain the molecular weight distribution of two polyether copolymers containing ethylene oxide and propylene oxide units. The measured molecular weights and their distributions were surprisingly different from the expected. Based upon the natural isotopic abundance, it was possible to provide a quantitative description of the number of ethylene oxide and propylene oxide units as a function of molecular weight. Important information on composition drift and heterogeneity can be obtained from the 3-D bivariate deconvolution of the mass spectra. As the molecular weight of a random copolymer increased, the ethylene oxide content also increased. A copolymer system with a narrow molecular weight distribution did not necessarily have a narrow composition distribution. These results provide information at the molecular level regarding the hydrophilicity of these copolymers used in polyurethane formulations.


1988 ◽  
Vol 10 (4) ◽  
pp. 682-690 ◽  
Author(s):  
DENNIS R. KLONNE ◽  
DAROL E. DODD ◽  
PATRICIA E. LOSCO ◽  
CATHERINE M. TROUP ◽  
TIPTON R. TYLER

Polymer ◽  
2018 ◽  
Vol 153 ◽  
pp. 167-172
Author(s):  
Shuangbin Fu ◽  
Yusheng Qin ◽  
Lijun Qiao ◽  
Xianhong Wang ◽  
Fosong Wang

1993 ◽  
Vol 5 (2) ◽  
pp. 189-201
Author(s):  
Dennis R. Klonne ◽  
Heather D. Burleigh-flayer ◽  
Darol E. Dodd ◽  
Patricia E. Losco ◽  
Tipton R. Tyler

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