4.7 Article

Pyrolysis mechanism of aliphatic amines bound to titania nanoparticles after H2O2 oxidation

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ELSEVIER
DOI: 10.1016/j.jaap.2022.105761

Keywords

Analytical pyrolysis; Multi-shot pyrolysis; Catalytic oxidation; TiO2 nanoparticles; Aliphatic amines; Peroxotitanates

Funding

  1. Ministry of Education, Youth and Sports of the Czech Republic [LM2018124]
  2. Southeast Asia - Europe Joint Funding project [LM2018124]
  3. [SEAEUROPEJFS19ST-076]

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Organic compounds bound to peroxotitanates can affect the photocatalytic activity of TiO2 nanoparticles after annealing. Understanding this influence is crucial for developing nanoparticles with desired catalytic behavior. A multi-analytical study was conducted to investigate the pyrolytic behavior of the organic fraction of amine-functionalized titania nanoparticles, revealing the formation of aromatic and heteroaromatic compounds during pyrolysis.
Organic compounds bound to peroxotitanates can influence the photocatalytic activity of TiO2 nanoparticles (NPs) obtained by subsequent annealing. Knowledge of how this influence plays out is fundamental for the development of NPs with desirable catalytic behavior, which can be used for several applications. Thermoana-lytical techniques can be used to simulate the annealing process on a small scale, but there is a lack of literature on this topic. This is especially true for nitrogen-containing organic compounds, which are not often used as organic modifiers in NP synthesis. Here, we present a multianalytical study of the pyrolytic behavior of the organic fraction of amine-functionalized titania NPs after peroxide treatment (namely peroxotitanate nano -particles modified with aliphatic amines). The study was carried out by TGA-MS, evolved gas analysis-mass spectrometry (EGA-MS) and double-shot analytical pyrolysis-GC-MS. The most abundant peaks in the GC-MS profiles obtained after thermal desorption were ascribed to nitriles, unsaturated hydrocarbons, and oxygen-ated compounds, whose total relative areas accounted for almost 100% for DPA and up to 70% for the other amines. This indicated that the presence of an N-Ti bond modulated the oxidating effect of hydrogen peroxide. Pyrolysis of the residual organic fraction on oxidized NPs underwent coupling reactions that led to the formation of aromatic species and, most interestingly, heteroaromatic compounds.

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