4.6 Article

Degradation of Deep-Eutectic Solvents Based on Choline Chloride and Carboxylic Acids

Journal

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
Volume 7, Issue 13, Pages 11521-11528

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.9b01378

Keywords

Deep-eutectic solvent; Decomposition; Carboxylic acid; Choline chloride; Malonic acid; Esterification

Funding

  1. Strategic Initiative Materials in Flanders (SIM), in the context of the Strategic Basic Research (SBO) program, SBO-SMART, Sustainable Metal Extraction from Tailings [HBC.2016.0456]
  2. Dutch Organization for Scientific Research (NWO) [ECHO.11.TD.006]

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Mixtures of carboxylic acids and choline chloride are one of the most commonly used families of deep-eutectic solvents. The thermal and long-term stability of carboxylic acid choline chloride (ChCl) deep-eutectic solvents was investigated. This family of DESs was found to degrade due to an esterification reaction, mainly between the carboxylic acid and the alcohol moiety of ChCl. The esterification reaction occurs even at room temperature over extended periods of time and is promoted at elevated temperatures. The esterification reaction takes place independently of the preparation method used. Moreover, the deep-eutectic solvent malonic acid-ChCl (x(ChCl) = 0.50) was found to decompose into acetic acid and carbon dioxide when prepared via the heating method, or when heated after preparation at room temperature. Therefore, the applicability of carboxylic acid-ChCl-based solvents is compromised.

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