<compilation>
 <compilers>William E. Acree, Jr.</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>3.524e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.524</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data>
    <exponent>-1</exponent>
    <number>6.925e-01</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>6.925</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>3.075e-01</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>3.075</significand>
    <unit>1</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>3.562e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.562</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data>
    <exponent>-1</exponent>
    <number>7.590e-01</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>7.590</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>2.410e-01</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>2.410</significand>
    <unit>1</unit>
   </data>
   <pntnum>2</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>3.590e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.590</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data>
    <exponent>-1</exponent>
    <number>8.185e-01</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>8.185</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>1.815e-01</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>1.815</significand>
    <unit>1</unit>
   </data>
   <pntnum>3</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>3.635e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.635</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data>
    <exponent>-1</exponent>
    <number>9.208e-01</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>9.208</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-2</exponent>
    <number>7.92e-02</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>3</sigfigs>
    <significand>7.92</significand>
    <unit>1</unit>
   </data>
   <pntnum>4</pntnum>
   <supplemental></supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>Differential scanning calorimeter. Mixtures (1.5 - 2.0 mg) of known concentration were weighed into aluminum pans, which were then crimped to preclude sample loss during the heating process. Solubilities determined by measuring melting points of binary mixtures using a Perkin-Elmer DSC-2 differential scanning calorimeter and scan rate of 5 K/min.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Djordjevic, N. M.; Thermochim. Acta 1991, 177, 109-118.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1016/0040-6031(91)80089-2</url>
 </sources>
 <substances>
  <casrn>83-32-9</casrn>
  <constituent>1</constituent>
  <formula>C12H10</formula>
  <inchi>InChI=1S/C12H10/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-6H,7-8H2</inchi>
  <inchikey>CWRYPZZKDGJXCA-UHFFFAOYSA-N</inchikey>
  <molweight>154.208</molweight>
  <name>Acenaphthene</name>
  <sample>99+%, Aldrich Chemical Company, Milwaukee, Wisconsin, USA, was used as received.</sample>
 </substances>
 <substances>
  <casrn>593-45-3</casrn>
  <constituent>2</constituent>
  <formula>C18H38</formula>
  <inchi>InChI=1S/C18H38/c1-3-5-7-9-11-13-15-17-18-16-14-12-10-8-6-4-2/h3-18H2,1-2H3</inchi>
  <inchikey>RZJRJXONCZWCBN-UHFFFAOYSA-N</inchikey>
  <molweight>254.494</molweight>
  <name>Octadecane</name>
  <sample>99%, Aldrich Chemical Company, was vacuum-distilled before use.</sample>
 </substances>
 <system>Acenaphthene with n-Octadecane</system>
 <title>Solubility data from IUPAC SDS Volume 58 (page 2) - Acenaphthene with n-Octadecane</title>
</compilation>