4.7 Article

Highly thermally stable multi-porous calcium aluminum hydrotalcite catalyst for efficient carbonate synthesis

Journal

FUEL
Volume 330, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2022.125696

Keywords

Catalytic chemistry; Dimethyl carbonate; Transesterification; Propylene carbonate; Solid base

Funding

  1. Liaoning Provincial Natural Science Foundation [2021NLTS-12-02]
  2. Key research and local service projects of Liaoning Provincial Department of Education [LDB2019005]
  3. JST SPRING [JPMJSP2145]
  4. JSPS KAKENHI [22J11458]

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A porous calcium aluminum hydrotalcite material was discovered in this study, showing excellent catalytic ability in transesterification reactions and outperforming traditional basic catalysts in stability and sustainability.
In the context of a carbon-neutral era, conversion of greenhouse gas CO2 via chemical catalysis is a powerful means. Using CO2 and petroleum-derived alkylene oxide as the raw materials to produce high-value carbonate substances has been considered a green and economic path for carbon reduction and energy transition. We discovered a multi-porous calcium aluminum hydrotalcite material (Ca-Al HT), and found that it performs excellent catalytic ability on transesterification (an important reaction in the synthesis of carbonates). Being different from homogeneous basic catalysts such as soluble metal hydroxides and organic halide salts, and well-known solid basic catalyst CaO, which are difficult to recycle and suffer severe deactivation in long-term catalytic process, the robust Ca12Al14O33 crystal phase in Ca-Al HT catalyst behaves much more stable catalytic performance during 4000 min efficient catalysis (63 % conversion and 100 % selectivity). The special crystal phase structure of Ca12Al14O33 remains stable at even a very high temperature of 900 degrees C. In contrast, CaO as the reference catalyst is very sensitive to trace H2O in catalytic system, and deactivates immediately. The outstanding catalytic ability of Ca-Al HT is attributed to its super-strong alkali strength, large alkali amount, and quick mass transfer originating from the hierarchical pore system.

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