TY - JOUR
T1 - Studies on degradation of poly(ethylene oxide) by multistep pyrolysis/gas chromatography with a programmable temperature vaporization injector
AU - Kaczmarek, H.
AU - Kowalonek, J.
AU - Janssen, J.G.M.
AU - Lieshout, van, H.P.M.
PY - 2000
Y1 - 2000
N2 - The multistep pyrolysis/gas chromatography technique using a programmable temperature vaporization injector was used to study thermal and photochemical properties of polymers. Pure poly(ethylene oxide) (PEOX) and PEOX + 3% CoCl2 specimens, 20-mm films, were UV-irradiated (2.45 mW/cm2) for 2 and 4 h in air at room temperature and pyrolyzed/gas chromatographed at 200°C, 420°C and 500°C (Fig. 1, 2). The products evolved at 200°C included residual solvent, monomer, catalyst, polymerization additives, and processing aids. At 420°C, degradation attained maximum and the compound concentrations were maximum in PEOX UV-irradiated for 2 h. In the 4-irradiated PEOX, the 420°C chromatographic peaks were less intense. At 500°C, the intensity of the peaks rose as the irradiation time was prolonged. CoCl2 (3%) gave rise to new degradation products. At 420°C and 500°C, irradiation had negligible effect on degradation of PEOX + 3% CoCl2. Scheme 1 illustrates the major interactions accompanying thermal and photochemical degradation of PEOX in the presence of CoCl2.
AB - The multistep pyrolysis/gas chromatography technique using a programmable temperature vaporization injector was used to study thermal and photochemical properties of polymers. Pure poly(ethylene oxide) (PEOX) and PEOX + 3% CoCl2 specimens, 20-mm films, were UV-irradiated (2.45 mW/cm2) for 2 and 4 h in air at room temperature and pyrolyzed/gas chromatographed at 200°C, 420°C and 500°C (Fig. 1, 2). The products evolved at 200°C included residual solvent, monomer, catalyst, polymerization additives, and processing aids. At 420°C, degradation attained maximum and the compound concentrations were maximum in PEOX UV-irradiated for 2 h. In the 4-irradiated PEOX, the 420°C chromatographic peaks were less intense. At 500°C, the intensity of the peaks rose as the irradiation time was prolonged. CoCl2 (3%) gave rise to new degradation products. At 420°C and 500°C, irradiation had negligible effect on degradation of PEOX + 3% CoCl2. Scheme 1 illustrates the major interactions accompanying thermal and photochemical degradation of PEOX in the presence of CoCl2.
M3 - Article
SN - 0032-2725
VL - 45
SP - 433
EP - 438
JO - Polimery
JF - Polimery
IS - 6
ER -