4.6 Article

Chitin Deacetylation Using Deep Eutectic Solvents: Ab Initio-Supported Process Optimization

期刊

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 9, 期 10, 页码 3874-3886

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.0c08976

关键词

chitin; deep eutectic solvents; greener deacetylation; density functional theory; deacetylation mechanism

资金

  1. Marine Biotechnology ERA-NET (European Commission's Seventh Framework Programme)
  2. BioApp project (Interreg V-A Italy-Slovenia)
  3. European Regional Development Fund
  4. Slovenian Research Agency [P2-0152, I0-0039]

向作者/读者索取更多资源

This study presents the use of deep eutectic solvents (DESs) for chitin deacetylation, offering an environmentally friendly alternative. The biocompatible DESs efficiently disrupt the native hydrogen-bonding network of chitin, readily dissolving it.
Chitin is the most abundant marine biopolymer, being recovered during the shell biorefining of crustacean shell waste. In its native form, chitin displays a poor reactivity and solubility in most solvents due to its extensive hydrogen bonding. This can be overcome by deacetylation. However, this process requires a high concentration of acids or bases at high temperatures, forming large amounts of toxic waste. Herein, we report on the first deacetylation with deep eutectic solvents (DESs) as an environmentally friendly alternative, requiring only mild reaction conditions. Biocompatible DESs are efficient in disturbing the native hydrogen-bonding network of chitin, readily dissolving it. First, quantum chemical calculations have been performed to evaluate the feasibility of different DESs to perform chitin deacetylation by studying their mechanism. Comparing these with the calculated barriers for garden-variety alkaline/acidic hydrolysis, which are known to proceed, prospective DESs were identified with barriers around 25 kcal.mol(-1) or lower. Based on density functional theory results, an experimental screening of 10 distinct DESs for chitin deacetylation followed. The most promising DESs were identified as K2CO3:glycerol (K2CO3:G), choline chloride:acetic acid ([Ch]Cl:AA), and choline chloride:malic acid ([Ch]Cl:MA) and were subjected to further optimization with respect to the water content, process duration, and temperature. Ultimately, [Ch]Cl:MA showed the best results, yielding a degree of deacetylation (DDA) of 40% after 24 h of reaction at 120 degrees C, which falls slightly behind the threshold value (50%) for chitin to be considered chitosan. Further quantum chemical calculations were performed to elucidate the mechanism. Upon the removal of 40% N-acetyl groups from the chitin structure, its reactivity was considerably improved.

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