4.7 Article

In-Situ Synthesis of TiO2@GO Nanosheets for Polymers Degradation in a Natural Environment

Journal

POLYMERS
Volume 13, Issue 13, Pages -

Publisher

MDPI
DOI: 10.3390/polym13132158

Keywords

polymers degradation; natural environment; photocatalyst; compounds

Funding

  1. National Natural Science Foundation of China [51703045]
  2. Zhejiang Provincial Natural Science Foundation of China [Y21E030023]

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Plastic photodegradation naturally takes a long time, and their chemical degradation typically requires additional energy or causes secondary pollution. The main components of global plastic are polymers, so new technologies are urgently needed to effectively decompose polymers in natural environments. This study successfully decomposes various polymers in a natural environment using the TiO2@GO photocatalyst and demonstrates that GO can enhance photocatalytic activity.
Plastic photodegradation naturally takes 300-500 years, and their chemical degradation typically needs additional energy or causes secondary pollution. The main components of global plastic are polymers. Hence, new technologies are urgently required for the effective decomposition of the polymers in natural environments, which lays the foundation for this study on future plastic degradation. This study synthesizes the in-situ growth of TiO2 at graphene oxide (GO) matrix to form the TiO2@GO photocatalyst, and studies its application in conjugated polymers' photodegradation. The photodegradation process could be probed by UV-vis absorption originating from the conjugated backbone of polymers. We have found that the complete decomposition of various polymers in a natural environment by employing the photocatalyst TiO2@GO within 12 days. It is obvious that the TiO2@GO shows a higher photocatalyst activity than the TiO2, due to the higher crystallinity morphology and smaller size of TiO2, and the faster transmission of photogenerated electrons from TiO2 to GO. The stronger fluorescence (FL) intensity of TiO2@GO compared to TiO2 at the terephthalic acid aqueous solution indicates that more hydroxyl radicals (center dot OH) are produced for TiO2@GO. This further confirms that the GO could effectively decrease the generation of recombination centers, enhance the separation efficiency of photoinduced electrons and holes, and increase the photocatalytic activity of TiO2@GO. This work establishes the underlying basic mechanism of polymers photodegradation, which might open new avenues for simultaneously addressing the white pollution crisis in a natural environment.

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