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(pet) and poly(ethylene terephthalate)-glycol

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MOLECULAR DYNAMICS IN POLY(ETHYLENE TEREPHTHALATE)<br />

(PET) AND POLY(ETHYLENE TEREPHTHALATE)-GLYCOL (PETG)<br />

M. Baranowski a) , A. Woźniak-Braszak a) , K. Jurga a) , J Jurga b) , K. Hołderna-Natkaniec a)<br />

a) High Pressure Physics Division, Institute of Physics, Adam Mickiewicz University,<br />

Umultowska 85, 61-614 Poznań, Pol<strong>and</strong><br />

e-mail:mikbar@ amu.edu.pl<br />

b) Polymer Processing Division, Institute of Materials Technology, Poznan University of<br />

Technology, Piotrowo 3, 61-138 Poznań, Pol<strong>and</strong><br />

e-mail:jan.jurga@put.poznan.pl<br />

The work presents the studies of molecular motions in two <strong>poly</strong>mers <strong>poly</strong>(<strong>ethylene</strong><br />

<strong>terephthalate</strong>) (PET) <strong>and</strong> amorphous co<strong>poly</strong>mer of PET <strong>poly</strong>(<strong>ethylene</strong> <strong>terephthalate</strong>)-<strong>glycol</strong><br />

(PETG) by solid-state NMR techniques. These <strong>poly</strong>mers have a great commercial <strong>and</strong><br />

industrial application in fibers, food containers, bottles, pharmaceutical packagings, toys etc<br />

[1, 2, 3]. The structures of these studied compounds were presented in Fig. 1.<br />

a)<br />

b)<br />

Fig. 1. Structure of a) PET<br />

b) PETG.<br />

The NMR methods were used to investigate the molecular dynamics. The spin – lattice<br />

proton T 1 measurements were carried out on home made pulse spectrometer operating at 30.2<br />

MHz, using a saturation sequence <strong>and</strong> “solid echo” to shorten the recovery time. The recovery<br />

of magnetization was single exponential. The temperature dependences of proton spin-lattice<br />

relaxation time T 1 for PET <strong>and</strong> PETG were shown in Fig.2. The second method of 1 H NMR<br />

lines was calculated from results of measurements performed on continuous wave<br />

spectrometer operating at 25 MHz. All experiments were conducted in temperature range<br />

from 140 to 375 K. Figure 3 shows the temperature dependence of the second moment of 1 H<br />

NMR line M 2 for both of researching <strong>poly</strong>mers. The model of internal dynamics was<br />

discussed.


Ea=11.3[kJ/mol]<br />

PETG<br />

PET<br />

T 1<br />

[s]<br />

1<br />

Ea=14.7[kJ/mol]<br />

0,1<br />

2,5 3,0 3,5 4,0 4,5 5,0 5,5 6,0<br />

1000/T [1/K]<br />

Fig.2. The temperature dependences of 1 H NMR spin-lattice relaxation time T 1 for<br />

PET <strong>and</strong> PETG, respectively.<br />

20<br />

18<br />

16<br />

14<br />

PETG<br />

PET<br />

M 2<br />

[G 2 ]<br />

12<br />

10<br />

8<br />

6<br />

4<br />

100 150 200 250 300 350 400<br />

T [K]<br />

Fig.3. The temperature dependence of the second moment M 2 of 1 H NMR line of PET<br />

<strong>and</strong> PETG, respectively.<br />

References:<br />

[1] C. P. Papadopoulou <strong>and</strong> N. K. Kalfoglou, Compatibility behaviour of blends of<br />

<strong>poly</strong>(<strong>ethylene</strong> <strong>terephthalate</strong>) with an amorphous co<strong>poly</strong>ester, POLYMER 38, Number<br />

3, (1997).<br />

[2] R.B. Dupaix, M. C. Boyce, Finite strain behavior of <strong>poly</strong>(<strong>ethylene</strong> <strong>terephthalate</strong>)<br />

(PET) <strong>and</strong> <strong>poly</strong>(<strong>ethylene</strong> <strong>terephthalate</strong>)-<strong>glycol</strong> (PETG), POLYMER 46 4827-4838<br />

(2005).<br />

[3] A. R. Donovan, G. Moad, A novel method for determination of <strong>poly</strong>ester end-groups<br />

by NMR spectroskopy, POLYMER 46 5005-5011 (2005).

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