Electrochemical reductive amination of furfural-based molecules
US-2018057949-A1 · Mar 1, 2018 · US
US11519083B1 · US · B1
| Field | Value |
|---|---|
| Publication number | US-11519083-B1 |
| Application number | US-202217853868-A |
| Country | US |
| Kind code | B1 |
| Filing date | Jun 29, 2022 |
| Priority date | Sep 13, 2021 |
| Publication date | Dec 6, 2022 |
| Grant date | Dec 6, 2022 |
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A method for preparing products by electrochemical reductive amination and simultaneous oxidation of aldehyde-based biomass using non-precious metal catalysts is provided, which relates to a field of electrocatalysis. The preparing method includes: performing an electrochemical reaction in an electrolytic system with room temperature and atmospheric pressure (at a range of 25° C. to 30° C., 101 kPa) by taking an aldehyde compound and an amine compound as raw materials for reductive amination and oxidation of aldehyde-based biomass, and thereby obtaining the products. The electrolytic system includes a reaction substrate, an electrolyte, a solvent, an anode and a cathode. The anode is a phosphorylated hydrotalcite catalyst and the cathode is a Ti-based catalyst. The method uses no external oxidants and precious metal catalysts, which is clean, environmental and efficient.
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What is claimed is: 1. A method for preparing products by electrochemical reductive amination and simultaneous oxidation of aldehyde-based biomass using non-precious metal catalysts, comprising: performing an electrochemical reaction in an electrolytic system with atmospheric pressure by taking an aldehyde compound and an amine compound as raw materials for the electrochemical reductive amination and simultaneous oxidation of aldehyde-based biomass, and thereby obtaining the products; wherein the electrolytic system comprises: a reaction substrate, an electrolyte, a solvent, an anode and a cathode; wherein for the simultaneous oxidation of aldehyde-based groups biomass, the cathode is a TiS 2 catalyst; wherein the anode is a phosphated nickel-cobalt layered double hydroxides (P—NiCo-LDHs) catalyst; the aldehyde compound is the reaction substrate, comprises: 5-hydroxymethyl furfural; and the electrolyte comprises an anode electrolyte and a cathode electrolyte. 2. The method according to claim 1 , wherein the solvent is ultrapure water. 3. The method according to claim 1 , wherein the cathode electrolyte is at least one of methylamine, ethylamine and ethanolamine. 4. The method according to claim 1 , wherein the anode electrolyte is at least one of sodium hydroxide and potassium hydroxide. 5. The method according to claim 1 , wherein a molar ratio of the aldehyde compound to the anode electrolyte is 1:0.5 to 1:10. 6. The method according to claim 1 , wherein a voltage of the electrochemical reaction relative to a reversible hydrogen electrode (RHE) is at a range from −0.6 V to 1.5 V. 7. The method according to claim 1 , wherein a temperature of the electrochemical reaction is at a range from 25° C. to 40° C. 8. The method according to claim 1 , wherein a temperature of the electrochemical reaction is at room temperature. 9. The method according to claim 1 , wherein a reaction time of the electrochemical reaction is at a range from 3 hours to 18 hours. 10. The method according to claim 1 , wherein a reaction time of the electrochemical reaction is at a range from 3 hours to 5 hours.
the compound being a non-noble metal oxide · CPC title
Reduction · CPC title
Nitrogen containing compounds · CPC title
Oxygen containing compounds · CPC title
Oxidation (halogenation C25B3/27) · CPC title
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