Synergic chemical analysis - the coupling of TG with FTIR, MS and GC-MS 2.Catalytic transformation of the gases evolved during the thermal decomposition of HDPE using acid-activated clays

High-density polyethylene, HDPE, has been thermally decomposed in a thermob alance and the evolved gases passed through a bed of catalyst. The resultin g tl transformation products were trapped and subsequently identified using GC-MS. Two smectites of different octahedral compositions were acid-activa ted under conditions known to produce catalysts of differing activity. Thre e different treatments were used for each smectite, thus providing six samp les for evaluation. The thermal and catalytic decomposition of HDPE was stu died under isothermal (60 min at 420 degreesC) and dynamic (35-650 degreesC at 10 degreesC min(-1)) conditions. The thermal decomposition of HDPE yiel ded characteristic quarters of peaks in the chromatogram which were assigne d to n-alkanes, l-alkenes, x-alkenes and alpha,omega -dienes in the range C -4-C-22 Species of higher molecular weight than C-22 were not detected. All six catalysts converted the alkenes present in the thermally generated off gases into light gases and aromatic species. Mono-, di- and trimethylbenze nes were the most abundant aromatic species although small quantities of et hylbenzenes and naphthalenes were produced. More aromatics were produced at 420 degreesC, than at temperatures up to 650 degreesC,whereas the reverse was true for branched alkanes. The total conversion of HDPE increased with both the extent of acid treatment and the process temperature, whereas the proportion of aromatics produced was greatest for catalysts prepared using short acid-treatment times. (C) 2000 Elsevier Science B.V. All rights reser ved.