Specific molecular structure changes and radical evolution during biomass-polyethylene terephthalate co-pyrolysis detected by 13C and 1H solid-state NMR
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作者:
Ko, Kwang-Hyun
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Univ New S Wales, Sch Mat Sci & Engn, Ctr Sustainable Mat Res & Technol SMaRT, Sydney, NSW 2052, AustraliaUniv New S Wales, Sch Mat Sci & Engn, Ctr Sustainable Mat Res & Technol SMaRT, Sydney, NSW 2052, Australia
Ko, Kwang-Hyun
[1
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Sahajwalla, Veena
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Univ New S Wales, Sch Mat Sci & Engn, Ctr Sustainable Mat Res & Technol SMaRT, Sydney, NSW 2052, AustraliaUniv New S Wales, Sch Mat Sci & Engn, Ctr Sustainable Mat Res & Technol SMaRT, Sydney, NSW 2052, Australia
Sahajwalla, Veena
[1
]
Rawal, Aditya
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Univ New S Wales, Mark Wainwright Analyt Ctr, Nucl Magnet Resonance Facil, Sydney, NSW 2052, AustraliaUniv New S Wales, Sch Mat Sci & Engn, Ctr Sustainable Mat Res & Technol SMaRT, Sydney, NSW 2052, Australia
Rawal, Aditya
[2
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[1] Univ New S Wales, Sch Mat Sci & Engn, Ctr Sustainable Mat Res & Technol SMaRT, Sydney, NSW 2052, Australia
[2] Univ New S Wales, Mark Wainwright Analyt Ctr, Nucl Magnet Resonance Facil, Sydney, NSW 2052, Australia
Co-pyrolysis of biomass with polyethylene terephthalate (PET) was studied as a function of blend ratio and co-pyrolysis temperature by C-13 and H-1 solid-state nuclear magnetic resonance (NMR). The C-13 NMR spectra showed that upon heating to 400 degrees C in presence of the biomass, the formation of crystallites in PET was completely suppressed and that at higher temperatures there was increased formation and growth of the polycyclic aromatic hydrocarbons ( PAHs). This change in the PET degradation behaviour was attributed to the presence of radicals formed in char from biomass. The measurement of the H-1-T-1 relaxation enabled monitoring the changes in the concentrations of radicals formed, as a function of the blend ratios and the co-pyrolysis temperatures. It indicated that the increase in the radical concentrations correlated well with the increased degradation of the PET and growth of PAHs. (C) 2014 Published by Elsevier Ltd.