Enzyme-catalyzed sequential reduction of carbon dioxide to formaldehyde

Wenfang Liu*, Yanhui Hou, Benxiang Hou, Zhiping Zhao

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

29 Citations (Scopus)

Abstract

It has been reported that enzymatic-catalyzed reduction of CO2 is feasible.Most of literature focuses on the conversion of CO2 to methanol.Hereinwe put emphasis on the sequential conversion of CO2 to formaldehyde and its single reactions. It appears that CO2 pressure plays a critical role and higher pressure is greatly helpful to form more HCOOH as well as HCHO. The reverse reaction became severe in the reduction of CO2 to formaldehyde after 10 h, decreasing HCHO production. Increasing the mass ratio of formate dehydrogenase to formaldehyde dehydrogenase could promote the sequential reaction. At concentrations of nicotinamide adenine dinucleotide lower than 100 mmol·L-1, the reduction of CO2 was accelerated by increasing cofactor concentration. The optimum pH value and concentration of phosphate buffer were determined as 6.0 and 0.05 mol·L-1, respectively, for the overall reaction. It seems that thermodynamic factor such as pH is restrictive to the sequential reaction due to distinct divergence in appropriate pH range between its single reactions.

Original languageEnglish
Pages (from-to)1328-1332
Number of pages5
JournalChinese Journal of Chemical Engineering
Volume22
Issue number11
DOIs
Publication statusPublished - 2014
Externally publishedYes

Keywords

  • Carbon dioxide
  • Enzymatic-catalyzed
  • Formaldehyde
  • Formic acid
  • Sequential reduction

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