Abstract
Low-density polyethylene (LDPE), polypropylene (PP), and their mixture in the mass ratio of 1: 1 (LDPE/PP) were thermally decomposed in a batch reactor at 450°C. The formed gaseous and oil/wax products were separated and analyzed by gas chromatography. The oils/waxes underwent both atmospheric and vacuum distillation. Densities, molar masses and bromine numbers of liquid distillates and distillation residues were determined. The first distillate fraction from the thermally decomposed LDPE contained mostly linear alkanes and alk-1-enes ranging from C6 to C13 (boiling point up to 180°C). The second distillate fraction was composed mostly of hydrocarbons C11 to C22 (boiling point up to 330°C). 2,4-Dimethylhept-1-ene was the major component of the first distillate fraction obtained from the product of PP decomposition, while in the 2nd distillate fraction it was 2,4,6,8-tetramethylundec-1-ene. The yields of some gaseous or liquid hydrocarbons obtained by distillation from thermally degraded LDPE/PP differed from the values corresponding to the decomposition of individual plastics due to the mutual influence of polyalkenes during their thermal cracking. Similarly, the yields of propene and methylpropene in the gaseous phase were higher in the case of mixture. Whereas the content of C9 to C17 alkanes and alkenes in the distillates separated from the liquid mixture obtained by the decomposition of LDPE/PP decreased, the formation of 2,4,6,8,10,12-hexamethylpentadec-1-ene remained unchanged. The corresponding mechanisms of thermal cracking were discussed.
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© 2007 Institute of Chemistry, Slovak Academy of Sciences
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Artikel in diesem Heft
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- Homo- and heteronuclear complexes of a new, vicinal dioxime ligand
- Synthesis of new triphenodithiazine- and indolocarbazolediones of biological interest
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