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Title: Controlled Assembly of Lignocellulosic Biomass Components and Properties of Reformed Materials

Journal Article · · ACS Sustainable Chemistry & Engineering
 [1];  [2];  [2];  [3]; ORCiD logo [2]; ORCiD logo [4];  [5]; ORCiD logo [6]; ORCiD logo [1];  [5];  [1]; ORCiD logo [7]; ORCiD logo [1]
  1. Univ. of Tennessee, Knoxville, TN (United States). Center for Renewable Carbon
  2. Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Materials Science and Technology Division
  3. Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Chemical and Engineering Materials Division, Center for Nanophase Materials Sciences
  4. Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Center for Nanophase Materials Sciences
  5. Univ. of Central Florida, Orlando, FL (United States). Nanoscience Technology Center
  6. Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Chemical and Engineering Materials Division
  7. Univ. of Tennessee, Knoxville, TN (United States). Center for Renewable Carbon; Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Materials Science and Technology Division

Reforming whole lignocellulosic biomass into value-added materials has yet to be achieved mainly due to the infusible nature of biomass and its recalcitrance to dissolve in common organic solvents. Recently, the solubility of biomass in ionic liquids (ILs) has been explored to develop all-lignocellulosic materials; however, efficient dissolution and therefore production of value-added materials with desired mechanical properties remain a challenge. This article presents an approach to producing high-performance lignocellulosic films from hybrid poplar wood. An autohydrolysis step that removes ≤50% of the hemicellulose fraction is performed to enhance biomass solvation in 1-ethyl-3-methyl imidazolium acetate ([C2mim][OAc]). The resulting biomass–IL solution is then cast into free-standing films using different coagulating solvents, yet preserving the polymeric nature of the biomass constituents. Methanol coagulated films exhibit a cocontinuous 3D-network structure with dispersed domains of less than 100 nm. The consolidated films with controllable morphology and structural order demonstrate tensile properties better than those of quasi-isotropic wood. Here, the methods for producing these biomass derivatives have potential for fabricating novel green materials with superior performance from woody and grassy biomass.

Research Organization:
Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)
Sponsoring Organization:
USDOE Office of Energy Efficiency and Renewable Energy (EERE)
Grant/Contract Number:
AC05-00OR22725
OSTI ID:
1394418
Journal Information:
ACS Sustainable Chemistry & Engineering, Vol. 5, Issue 9; ISSN 2168-0485
Publisher:
American Chemical Society (ACS)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 20 works
Citation information provided by
Web of Science

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Cited By (4)

Dynamics of the lignin glass transition journal January 2018
A fundamental understanding of whole biomass dissolution in ionic liquid for regeneration of fiber by solution-spinning journal January 2019
Relationship between lignocellulosic biomass dissolution and physicochemical properties of ionic liquids composed of 3-methylimidazolium cations and carboxylate anions journal January 2018
Structural changes in lignocellulosic biomass during activation with ionic liquids comprising 3-methylimidazolium cations and carboxylate anions journal September 2018