Title Krafft temperature and enthalpy of solution of N-acyl amino acid ...
Title Krafft temperature and enthalpy of solution of N-acyl amino acid ...
Title Krafft temperature and enthalpy of solution of N-acyl amino acid ...
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Results<br />
Solubility<br />
Figure 2 shows the logarithm <strong>of</strong> the solubility <strong>of</strong> N-hexadecanoyl<br />
<strong>amino</strong> <strong>acid</strong> sodium salts obtained by HPLC as a function <strong>of</strong> <strong>temperature</strong>.<br />
For C16-DL-Ile, its solubility could not be determined because its KT was<br />
below 0 °C. From Figure 2 it can be seen that the solubility rises abruptly<br />
at a particular <strong>temperature</strong> in all systems. The <strong>temperature</strong>s correspond to<br />
the KT <strong>and</strong> these values are summarized in Table 2. The order <strong>of</strong> KT was<br />
C16-Ile < -Leu < -Val < -Phe < -Ala, which increased with decreasing size<br />
<strong>of</strong> residue except for C16-Phe. For the C16-Ala <strong>and</strong> C16-Phe systems,<br />
the KT <strong>of</strong> the DL form was higher than that <strong>of</strong> the L form. Conversely,<br />
for the C16-Val, C16-Leu, <strong>and</strong> C16-Ile systems the KT <strong>of</strong> the DL form was<br />
lower than that <strong>of</strong> the L form. Furthermore the solubility <strong>of</strong> C16-Phe<br />
below the KT was smaller one order <strong>of</strong> magnitude compared with the other<br />
systems, <strong>and</strong> its <strong>temperature</strong> dependence was much larger. This means<br />
that <strong>enthalpy</strong> <strong>of</strong> <strong>solution</strong> <strong>of</strong> C16-Phe is substantial as described in the next<br />
section.<br />
DSC<br />
The thermograms <strong>of</strong> a 10mM aqueous <strong>solution</strong> <strong>of</strong> Na N-hexadecanoyl<br />
<strong>amino</strong> <strong>acid</strong> surfactants in the presence <strong>of</strong> the solid deposit are shown in Fig.<br />
3. It can be seen that an endothermic peak accompanies the dis<strong>solution</strong> <strong>of</strong><br />
the surfactant around the KT. In this measurement, KT could be defined<br />
as the <strong>temperature</strong> corresponding to the onset <strong>of</strong> the peak <strong>and</strong> these values<br />
are shown in Table 2. The KT values determined by this method gave a<br />
6