4.8 Review

Oxide-Zeolite-Based Composite Catalyst Concept That Enables Syngas Chemistry beyond Fischer-Tropsch Synthesis

Journal

CHEMICAL REVIEWS
Volume 121, Issue 11, Pages 6588-6609

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemrev.0c01012

Keywords

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Funding

  1. Ministry of Science and Technology of China [2016YFA0202803, 2018YFA0704503]
  2. Chinese Academy of Sciences [XDA21020400]
  3. National Natural Science Foundation of China [91945302, 22002153, 22008234]
  4. Youth Innovation Promotion Association of Chinese Academy of Sciences Sciences [2019184]
  5. Dalian High Level Talent Innovation Support Program [2017RD09]
  6. Leading Talent Program of Technology Innovation for Prospering Liaoning [XLYC1802130]

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The OXZEO catalyst concept enables high selectivity in the direct conversion of syngas to light olefins and ethylene, surpassing the theoretical limits of conventional FTS. It also allows the synthesis of gasoline-range isoparaffins and aromatic compounds. This concept demonstrates versatility and may serve as a technology platform for utilizing carbon resources to produce chemicals and fuels.
Syngas chemistry has been under study since Fischer-Tropsch synthesis (FTS) was invented in the 1920s. Despite the successful applications of FTS as the core technology of coal-to-liquid and gas-to-liquid processes in industry, the product selectivity control of syngas conversion still remains a great challenge, particularly for value-added chemicals such as light olefins. Recent studies show that the catalyst design concept of OXZEO (oxide-zeolite-based composite) enables direct syngas conversion to mixed light olefins with a selectivity reaching 80% and to ethylene with a selectivity of 83% among hydrocarbons. They both well-surpass the limits predicated by the Anderson-Schultz-Flory model via the conventional FTS route (58% and 30%, respectively). Furthermore, this catalyst concept allows one-step synthesis of gasoline-range isoparaffins and aromatic compounds, which is otherwise not possible in conventional FTS. A rapidly growing number of studies demonstrate the versatility of this concept and may form a technology platform for utilization of carbon resources including coal, natural gas, and biomass via syngas to a variety of basic chemicals and fuels. However, the selectivity control mechanism is far from being understood. Therefore, we focus mainly on the catalytic roles of the bifunctionalities of OXZEO while reviewing the development of bifunctional catalysts for selective syngas conversion by taking syngas-to-light olefins as an example. With this, we intend to provide insights into the selectivity control mechanism of the OXZEO concept in order to understand the challenges and prospects for future development of much more active and more selective catalysts.

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