期刊
POLYMER
卷 55, 期 1, 页码 340-346出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.polymer.2013.08.018
关键词
Poly(styrene-co-divinylbenzene); Porous monolith; Hypercrosslinked polymer
资金
- Office of Science, Office of Basic Energy Sciences, Scientific User Facilities Division of the U.S. Department of Energy [DE-AC02-05CH11231]
- ME-Fulbright fellowship
Poly(styrene-divinylbenzene) monoliths have been hypercrosslinked using a Fe3+ catalyzed Friedel Crafts reaction involving three external crosslinkers (1) 4,4'-bis(chloromethyl)-1,1'-biphenyl, (2) axedichloro-p-xylene, and (3) formaldehyde dimethyl acetal. The first crosslinker was found to produce monoliths with the best chromatographic performance. The effects of a number of variables affecting the hypercrosslinking reaction were studied in detail. These variables included: (i) the temperature and time used for polymerization of the precursor monoliths, (ii) the amount and loading procedure of the external crosslinker and catalyst, and, (iii) the temperature and reaction time of the Friedel Crafts alkylation. Polymers with extremely large surface areas reaching up to 900 m(2)/g were obtained using a precursor monolith polymerized for only 2.5 h, and hypercrosslinked with 4,4'-bis(chloromethyl)-1,1'-biphenyl. The increased performance of monoliths modified using this new procedure is comparable to the performance obtained with monolithic polymers containing chloromethylstyrene. However, the preparation of the poly(styrene-divinylbenzene) precursor is simpler than that of conterparts containing chloromethylstyrene. The hypercrosslinked monoliths in capillary columns were tested in an isocratic reversed phase liquid chromatography separation using a mixture comprised of acetone and six alkyl-benzenes. Column efficiencies for retained analytes exceeded 70,000 plates/m. (C) 2013 Elsevier Ltd. All rights reserved.
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