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Depolymerization of poly(trimethylene terephthalate) in supercritical methanol

✍ Scribed by Hao-Hong Zhang; Hong-Wei Xiang; Yong Yang; Yuan-Yuan Xu; Yong-Wang Li


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
104 KB
Volume
92
Category
Article
ISSN
0021-8995

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✦ Synopsis


Abstract

The depolymerization of poly(trimethylene terephthalate) (PTT) in supercritical methanol was carried out with a batch‐type autoclave reactor at temperatures ranging from 280 to 340Β°C, at pressures ranging from 2.0 to 14.0 MPa, and for reaction time of up to 60 min. PTT quantitatively decomposed into dimethyl terephthalate (DMT) and 1,3‐propaniol (PDO) under the designed conditions. The yields of DMT and PDO greatly increased as the temperature rose. The yields of the monomers markedly increased as the pressure increased to 10.0 MPa, and they leveled off at higher pressures. The final yield of DMT at 320Β°C and 10.0 MPa reached 98.2%, which was much closer to the extent of the complete reaction. A kinetic model was used to describe the depolymerization reaction, and it fit the experimental data well. The dependence of the forward rate constant on the reaction temperature was correlated with an Arrhenius plot, which gave an activation energy of 56.8 kJ/mol. Β© 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 2363–2368, 2004


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Heat capacity of poly(trimethylene terep
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The heat capacity of poly(trimethylene terephthalate) (PTT) has been measured using adiabatic calorimetry, standard differential scanning calorimetry (DSC), and temperature-modulated differential scanning calorimetry (TMDSC). The heat capacities of the solid and liquid states of semicrystalline PTT