4.4 Article

Preparation of graphitic carbon nitride g-C3N4-HMCM-22 composite catalysts and enhanced para-selectivity in m-xylene isomerization

Journal

CHEMICAL PAPERS
Volume 76, Issue 3, Pages 1875-1884

Publisher

SPRINGER INT PUBL AG
DOI: 10.1007/s11696-021-01982-4

Keywords

m-xylene; p-xylene; Isomerization; g-C3N4-HMCM-22 catalyst

Funding

  1. National Natural Science Foundation of China [21878027]
  2. Advanced Catalysis and Green Manufacturing Collaborative Innovation Center [ACGM2020-08]
  3. Natural Science Foundation of the Jiangsu Higher Education Institutions [18KJA150001, 19KJA430003]
  4. Foundation of State Key Laboratory of High-efficiency Utilization of Coal and Green Chemical Engineering [2017-K28]

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A series of novel g-C3N4-HMCM-22 composite catalysts were successfully prepared and characterized. The introduction of g-C3N4 was found to improve the selectivity in m-xylene isomerization, with the G1H1 composite catalyst showing the highest selectivity. The study suggests that increasing the number of Lewis acid sites and inhibiting the external Bronsted acid sites of HMCM-22 are crucial for improving the selectivity.
A series of novel graphitic carbon nitride g-C3N4-HMCM-22 composite catalysts were successfully prepared. Their structure and acid properties were well characterized by thermogravimetric analysis (TGA), X-ray diffraction (XRD), N-2 adsorption-desorption, Fourier transform infrared spectroscopy (TFIR), X-ray photoelectron spectroscopy (XPS), Scanning Electron Microscopy (SEM), and Py-FTIR. The prepared g-C3N4-HMCM-22 composite catalysts were then used for m-xylene (MX) isomerization. The effect of introduction of g-C3N4 on catalytic performance was studied. Compared with parent HMCM-22 catalyst, g-C3N4-HMCM-22 composite catalysts exhibited an improved p-xylene (PX) selectivity in MX isomerization. Moreover, G1H1 composite catalyst showed the highest PX selectivity than other as-prepared composite samples. Correlating the catalyst performance with its physical and chemical properties uncovers that increasing amounts of Lewis acid sites and effectively inhibiting the external Bronsted acid sites of HMCM-22 would be the key to improving the selectivity of PX.

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