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Solubilization logarithmic-linear

In dilute solutions, the solute will, on average, contact only one hydrated cosolvent molecule at a time, and the degree of solubilization should be a linear rather than a logarithmic function of cosolvent content. Thus, it is expected that the log-linear relationship between Sm andf. that applies at high cosolvent concentrations will become linear at low cosolvent levels due to a change in the mechanism of solubilization. If S is defined as solubility enhancement... [Pg.143]

For non-polar solutes, or those solutes that are more non-polar than the cosolvent of choice, solubilization generally follows the log-linear model of Eq. (18). The degree of solubilization is directly related to the polarity of the solute. From Eq. (20) it has been shown that the solubilization slope, octanol-water partition coefficient (logAio/w)- Fig- 6 shows data for a series of hydrocortisones in propylene glycol. As log Mo/w increases it follows that the solubilization slopes increase. Li and Yalkowsky have also illustrated this relationship for non-polar solutes in ethanol-water... [Pg.3320]


See other pages where Solubilization logarithmic-linear is mentioned: [Pg.317]    [Pg.116]    [Pg.30]    [Pg.207]    [Pg.168]    [Pg.2979]    [Pg.3319]    [Pg.313]    [Pg.790]    [Pg.476]    [Pg.790]    [Pg.447]    [Pg.170]    [Pg.239]    [Pg.194]    [Pg.199]   
See also in sourсe #XX -- [ Pg.809 ]




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