Encapsulation of catalyst in block copolymer micelles for the polymerization of ethylene in aqueous medium

被引:58
|
作者
Boucher-Jacobs, Camille [1 ]
Rabnawaz, Muhammad [1 ,3 ]
Katz, Joshua S. [2 ]
Even, Ralph [2 ]
Guironnet, Damien [1 ]
机构
[1] Univ Illinois, Dept Chem & Biomol Engn, Urbana, IL 61801 USA
[2] Dow Chem Co USA, Corp Res & Dev, Formulat Sci, Collegeville, PA 19426 USA
[3] Michigan State Univ, Sch Packaging, 130 Packaging Bldg,448 Wilson Rd, E Lansing, MI 48824 USA
来源
NATURE COMMUNICATIONS | 2018年 / 9卷
关键词
TRANSITION-METAL-COMPLEXES; POSSIBLE SIDE REACTIONS; EMULSION POLYMERIZATION; DISPERSION POLYMERIZATION; INSERTION POLYMERIZATION; ROOM-TEMPERATURE; MOLECULAR-WEIGHT; CROSS-COUPLINGS; WATER; NANOREACTORS;
D O I
10.1038/s41467-018-03253-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The catalytic emulsion polymerization of ethylene has been a long-lasting technical challenge as current techniques still suffer some limitations. Here we report an alternative strategy for the production of semi-crystalline polyethylene latex. Our methodology consists of encapsulating a catalyst precursor within micelles composed of an amphiphilic block copolymer. These micelles act as nanoreactors for the polymerization of ethylene in water. Phosphinosulfonate palladium complexes were used to demonstrate the success of our approach as they were found to be active for hours when encapsulated in micelles. Despite this long stability, the activity of the catalysts in micelles remains significantly lower than in organic solvent, suggesting some catalyst inhibition. The inhibition strength of the different chemicals present in the micelle were determined and compared. The combination of the small volume of the micelles, and the coordination of PEG appear to be the culprits for the low activity observed in micelles.
引用
收藏
页数:9
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