A b " , D. S.; Raumltz, J. M. Am. Inst. Chem. €ng. J . 1975. 21, 116. 250. R m . H.; Rausnttz. J. M. Am. Inst. Chem. €ng. J . 1968, 74. 135. chemlcel€ng)wenhg; John wlley a Sons: New York. 1981. Blenco, A.; Mea, J. M.; Arce. A.: Conea, A. Can. J . Chem. €ng. 1988, 86. 138.(9) Roddy. J. W.; Coleman. C. F. Ind. w . Ckm. Fudem. 1981, 20, Hsnky, E. J.; m. J. D. E m -s b p g e " d b n Operebbns h The eolu#mkr of ethylbenzene and 1,2-, 1,3-, and 1,4dhnethylbenzene In aqueous sodium chkrMe sohtiono having knk strengths ranglng from 0 to 5.00 mol dmJ have been detmIned at 298.15 K. The sohbiiltles were detcnmined by headspace analysis using a multlpkkr/.cth interrupted4low (MIIF) technique. The values for the Henry's law constants and aqueous/vapor partlth coefficients for the compounds in the odutions dudhd are a b ghren. Corrdatknr between the
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.