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Alkaline hydiolysis of PET
ACID HYDROLYSIS OF PET
Impact of hydrolytic degradation on mechanical properties of PET -
Towards an understanding of microplastics formation
Ocean pollution by microplastics, i.e. small pieces of plastic of less than 5 mm, is one of the major
concerns for the future of our planet. Secondary microplastics formation is due to fragmentation of
macroplastic waste. This fragmentation can be attributed to environmental loadings such as waves,
winds and tides, coupled with a change in mechanical properties of polymers induced by UV and
seawater ageing. This study aims to characterize and understand changes in the mechanical
behaviour of Polyethylene Terephthalate (PET) induced by hydrolysis, especially for high
degradation levels. Thin films (200 μm) of PET were aged in water at temperatures from 110 °C to
80 °C for up to 150 days. Embrittlement occurs with chain scission during hydrolysis when molar
mass of the polymer falls below 17 kg/mol. When the polymer is brittle, i.e. for high levels of
degradation, the stress at break decreases linearly with the molar mass, and can be described by a
simple mathematical expression.
An FT–IR study of the effect of hydrolytic degradation on the structure
of thin PET film
Chris Sammon a, Jack Yarwood a, Neil Everall b
Thin (∼100 nm) PET films were treated in pure water and 1% KOH solution and changes in the chemistry and
morphology were followed using FTIR–RAIRS. Degradation was monitored using the intensity of the alcohol and acid ν
(OH) bands. Dramatic changes in intensity of the ν(C–H) band were noted as a function of degradation for both samples
treated in pure water and KOH solution. This was interpreted as resulting from a change in the environment of the
aliphatic methyl groups and subsequent extensive hydrogen bonding, due to an increase in the numbers of hydrophilic
end groups. Differences in the OH) and ν
(CO) bandshapes were noted between the two systems suggesting different hydrogen bonded species. The autocatalytic
nature of the hydrolysis in pure water was confirmed and evidence of the so-called ‘chemicrystallisation' effect, with
crystallinity increasing with degradation, was observed. The thin nature of the films allowed a spectroscopic insight into
the morphology of the degrading films as a function of treatment time.
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Alkaline and acid hydrolysis of Polyethylene Terapthalate (PET)

  • 2.
  • 3.
  • 4.
  • 6.
  • 7.
  • 8. Impact of hydrolytic degradation on mechanical properties of PET - Towards an understanding of microplastics formation Ocean pollution by microplastics, i.e. small pieces of plastic of less than 5 mm, is one of the major concerns for the future of our planet. Secondary microplastics formation is due to fragmentation of macroplastic waste. This fragmentation can be attributed to environmental loadings such as waves, winds and tides, coupled with a change in mechanical properties of polymers induced by UV and seawater ageing. This study aims to characterize and understand changes in the mechanical behaviour of Polyethylene Terephthalate (PET) induced by hydrolysis, especially for high degradation levels. Thin films (200 μm) of PET were aged in water at temperatures from 110 °C to 80 °C for up to 150 days. Embrittlement occurs with chain scission during hydrolysis when molar mass of the polymer falls below 17 kg/mol. When the polymer is brittle, i.e. for high levels of degradation, the stress at break decreases linearly with the molar mass, and can be described by a simple mathematical expression.
  • 9. An FT–IR study of the effect of hydrolytic degradation on the structure of thin PET film Chris Sammon a, Jack Yarwood a, Neil Everall b Thin (∼100 nm) PET films were treated in pure water and 1% KOH solution and changes in the chemistry and morphology were followed using FTIR–RAIRS. Degradation was monitored using the intensity of the alcohol and acid ν (OH) bands. Dramatic changes in intensity of the ν(C–H) band were noted as a function of degradation for both samples treated in pure water and KOH solution. This was interpreted as resulting from a change in the environment of the aliphatic methyl groups and subsequent extensive hydrogen bonding, due to an increase in the numbers of hydrophilic end groups. Differences in the OH) and ν (CO) bandshapes were noted between the two systems suggesting different hydrogen bonded species. The autocatalytic nature of the hydrolysis in pure water was confirmed and evidence of the so-called ‘chemicrystallisation' effect, with crystallinity increasing with degradation, was observed. The thin nature of the films allowed a spectroscopic insight into the morphology of the degrading films as a function of treatment time.