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Rapid Depolymerization of Decrystallized Cellulose to Soluble Products via Ethanolysis under Mild Conditions
Author(s) -
Tyufekchiev Maksim,
Ralph Katherine,
Duan Pu,
Yuan Shichen,
SchmidtRohr Klaus,
Timko Michael T.
Publication year - 2020
Publication title -
chemsuschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.412
H-Index - 157
eISSN - 1864-564X
pISSN - 1864-5631
DOI - 10.1002/cssc.201903446
Subject(s) - depolymerization , cellulose , hydrolysis , chemistry , solvent , ball mill , organic chemistry , polymerization , chemical engineering , materials science , polymer , engineering
Efficient cellulose depolymerization is a major bottleneck for economical production of second‐generation biofuels. In this work, crystalline cellulose was subjected to sequential ball milling and ethanolysis as a mild and selective depolymerization approach. Ball milling and ethanolysis resulted in 38±1 % cellulose conversion, with 24 % ethyl‐glucopyranoside as the main identified and quantified product and negligible side reaction of the ethanol solvent to form diethyl ether. In comparison, ethanolysis of the original cellulose resulted in only 3±1 % conversion. Additional soluble products from cellulose ethanolysis included carbohydrate isomers and oligomers, differing from the products obtained from hydrolysis. X‐ray diffraction and nuclear magnetic resonance spectroscopy revealed increased crystallinity post‐reaction, retarding further depolymerization. Hot liquid water extracted soluble oligomers from the ethanolyzed cellulose, suggesting formation of a nanoscale barrier of crystalline cellulose that traps soluble products during ethanolysis. Use of cellulose‐swelling co‐solvents and repeated mechanical decrystallization both proved effective at increasing cellulose conversion and soluble product yields. Repeated ball milling and ethanolysis resulted in 62±1 % cellulose conversion. Ethanolysis of decrystallized cellulose has potential for rapid (<2 h) de‐polymerization at mild conditions.