کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5186119 | 1381096 | 2007 | 10 صفحه PDF | دانلود رایگان |
The thermal decomposition of the organic free-radical initiator, diethyl peroxydicarbonate (DEPDC), was monitored by in situ ATR-FT-IR in heptane, and in the green solvent supercritical carbon dioxide (scCO2) both with and without supercritical ethylene. It was observed that the characteristic peaks of DEPDC at 1802-1803 and 1194-1203 cmâ1 decreased significantly upon heating corresponding to the decomposition of DEPDC, while two new intense peaks simultaneously appeared at 1747 and 1262 cmâ1 in heptane, and similarly at 1756 and 1250 cmâ1 in scCO2. The changes in the absorbance intensity of the characteristic peaks of the initiator during the decomposition were used for the measurement of the decomposition rate constant (kd) of DEPDC. It was found that the thermal decomposition of DEPDC at low concentration in either heptane under atmospheric N2 or scCO2 under high pressure was via the first-order kinetics of unimolecular decomposition. The activation energy of the thermal decomposition of DEPDC was found to be 115 kJ/mol in heptane from 40 to 74 °C and 118 kJ/mol in scCO2 from 40 to 60 °C. These new peaks revealed the formation of carboxyl groups contained in the decomposed products, indicating incomplete decarboxylation. During removal of CO2 after the reaction in scCO2, the instable intermediate monoethyl carbonate was decarboxylated and converted into the major end product, ethanol.
Journal: Polymer - Volume 48, Issue 5, 23 February 2007, Pages 1219-1228