Chinese Journal of Catalysis ›› 2018, Vol. 39 ›› Issue (6): 1060-1069.DOI: 10.1016/S1872-2067(18)63019-0

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Acid-promoted Ir-La-S/AC-catalyzed methanol carbonylation on single atomic active sites

Zhou Rena,c, Yuan Lyua, Siquan Fenga,c, Xiangen Songa, Yunjie Dinga,b   

  1. a Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China;
    b State Key Laboratory of catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China;
    c University of Chinese Academy of Sciences, Beijing 100049, China
  • Received:2018-01-19 Revised:2018-03-02 Online:2018-06-18 Published:2018-05-16
  • Contact: 10.1016/S1872-2067(18)63019-0
  • Supported by:

    This work was supported by the National Key R&D Program of China (2017YFB0602203).

Abstract:

Highly active Ir-La-S/AC catalyst was successfully prepared by co-impregnation of an activated carbon (AC) carrier with a sulfuric acid solution of Ir and La species and compared with a traditionally prepared Ir-La/AC catalyst. High angle annular dark-field-scanning transmission electron microscopy (HAADF-STEM) measurement results show that most of the Ir species on Ir-La-S/AC exist as single atomic sites, while those on Ir-La/AC exist as nanoparticles with an average diameter of 1.5 nm. Evaluation of Ir-La-S/AC as a catalyst for heterogeneous carbonylation of methanol to acetyl gave a maximum TOF (turn-over-frequency) of 2760 h-1, which was distinctly higher than that achieved by the Ir-La/AC catalyst (approximately 1000 h-1). Temperature-programmed desorption of ammonia (NH3-TPD) result shows that the addition of sulfuric acid during the preparation procedure results in significantly more acidic sites on Ir-La-S/AC than those on Ir-La/AC, which plays a key role in the enhancement of CO insertion as the rate-determining step. Temperature-programmed reduction (TPR) and in situ X-ray photoelectron spectroscopy reveal that Ir species are more reducible, and that more Ir+ might be formed by activation of Ir-La-S/AC than those on the Ir-La/AC catalyst, which is thought to be beneficial for reductive elimination of AcI from Ir3+ species as an essential step for CH3I regeneration and acetyl formation.

Key words: Heterogeneous methanol carbonylation, Ir-La-S/AC catalyst, Bifunctional catalyst, Single-atomic active site, Co-impregnation