4.7 Article

On-line photoionization mass spectrometric study of the catalytic pyrolysis of acrylonitrile-butadiene-styrene copolymer over HZSM-5, HUSY and Al-MCM-41

Journal

FUEL
Volume 307, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2021.121937

Keywords

On-line analysis; Photoionization; Mass spectrometry; Catalytic pyrolysis; ABS copolymer; Molecular sieve

Funding

  1. Shanghai Research Institute of Petrochemical Technology [20/BZY20-HG-001]
  2. National Natural Science Foundation of China [91845203, 91945302, 92045301, 52176197]
  3. CAS Key Technology Talent Program

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Three molecular sieve-based catalysts, HZSM-5, HUSY, and Al-MCM-41, were utilized in the catalytic pyrolysis of ABS copolymer, with HZSM-5 and HUSY showing significant suppression of N-containing oligomers formation while Al-MCM-41 producing large amounts of polycyclic aromatic hydrocarbons. HUSY demonstrated better denitrogenation ability compared to HZSM-5. The study highlights the potential of SVUV-PIMS in investigating catalytic decomposition mechanisms of complex copolymers.
Three molecular sieve-based catalysts, HZSM-5, HUSY, and Al-MCM-41, were employed in the catalytic pyrolysis of acrylonitrile-butadiene-styrene (ABS) copolymer. The on-line synchrotron vacuum ultraviolet photoionization mass spectrometry (SVUV-PIMS) together with pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) was used to evaluate the performances of these catalysts in the catalytic pyrolysis processes, especially their denitrogenation ability on the pyrolysis oil. Based on the Py-GC/MS results, the formation of N-containing oligomers can be significantly suppressed with the presence of HZSM-5 and HUSY, over which a high content of Bronsted acid sites were detected. In contrast, although large amounts of polycyclic aromatic hydrocarbons can be formed over Al-MCM-41, little effect was exhibited on the yields of major products owing to its inferior acidity. Given the relative production of light nitrogenous compounds, it can be concluded that HUSY is more applicable to the denitrogenation than HZSM-5. On account of the temperature-evolved profiles of the aromatic products acquired with SVUV-PIMS in real time, two different reaction paths were proposed for the catalytic pyrolysis over zeolite catalysts, by which the formation of valuable compounds can be clearly demonstrated, including benzene, toluene, ethylbenzene, and styrene. Moreover, it has been directly evidenced that the framework structure of HUSY can facilitate intermolecular hydrogen transfer to a great extent. This work highlights the superiority of SVUV-PIMS in the study of catalytic decomposition mechanisms of complex copolymers.

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