|کد مقاله||کد نشریه||سال انتشار||مقاله انگلیسی||ترجمه فارسی||نسخه تمام متن|
|200579||460476||2016||12 صفحه PDF||سفارش دهید||دانلود رایگان|
• Heat capacities of selected alcohols were determined by Tian-Calvet calorimetry.
• Results were compared with selected estimation methods.
• Phase behavior was explored by differential scanning calorimetry.
• Calorimetric measurements were complemented by FTIR spectroscopy.
Isobaric liquid phase heat capacities of nine selected aliphatic heptanols (1-heptanol, CAS RN: 111-70-6; 3-heptanol, CAS RN: 589-82-2; 4-heptanol, CAS RN: 589-55-9; 2-methyl-2-hexanol, CAS RN: 625-23-0; 5-methyl-2-hexanol, CAS RN: 627-59-8; 2-methyl-3-hexanol, CAS RN: 617-29-8; 3-ethyl-3-pentanol, CAS RN: 597-49-9; 2,2-dimethyl-3-pentanol, CAS RN: 3970-62-5; 2,4-dimethyl-3-pentanol, CAS RN: 600-36-2) were measured with a highly sensitive Tian-Calvet calorimeter in the temperature range from 261 K to 382 K. Experimental heat capacity data were correlated as a function of temperature. For eight compounds, a maximum on temperature dependence of heat capacity was observed. The phase behavior was investigated with a differential scanning calorimeter. Calorimetric measurements were complemented by FTIR spectroscopy from room temperature to a maximum of 428 K. The main aim of this work was to fill the gap in reliable heat capacity data for these compounds and to extend the knowledge base required for a better understanding of alcohols self-association.
Figure optionsDownload as PowerPoint slide
Journal: Fluid Phase Equilibria - Volume 423, 15 September 2016, Pages 43–54