Abstract
Here, we report a novel ammonia : ammonium salt solvent based pretreatment process that can rapidly dissolve crystalline cellulose into solution and eventually produce highly amorphous cellulose under near-ambient conditions. Pre-activating the cellulose I allomorph to its ammonia-cellulose swollen complex (or cellulose III allomorph) at ambient temperatures facilitated rapid dissolution of the pre-activated cellulose in the ammonia-salt solvent (i.e., ammonium thiocyanate salt dissolved in liquid ammonia) at ambient pressures. For the first time in reported literature, we used time-resolved in situ neutron scattering methods to characterize the cellulose polymorphs structural modification and understand the mechanism of crystalline cellulose dissolution into a 'molecular' solution in real-time using ammonia-salt solvents. We also used molecular dynamics simulations to provide insight into solvent interactions that non-covalently disrupted the cellulose hydrogen-bonding network and understand how such solvents are able to rapidly and fully dissolve pre-activated cellulose III. Importantly, the regenerated amorphous cellulose recovered after pretreatment was shown to require nearly ∼50-fold lesser cellulolytic enzyme usage compared to native crystalline cellulose I allomorph for achieving near-complete hydrolytic conversion into soluble sugars. Lastly, we provide proof-of-concept results to further showcase how such ammonia-salt solvents can pretreat and fractionate lignocellulosic biomass like corn stover under ambient processing conditions, while selectively co-extracting ∼80-85% of total lignin, to produce a highly digestible polysaccharide-enriched feedstock for biorefinery applications. Unlike conventional ammonia-based pretreatment processes (e.g., Ammonia Fiber Expansion or Extractive Ammonia pretreatments), the proposed ammonia-salt process can operate at near-ambient conditions to greatly reduce the pressure/temperature severity necessary for conducting effective ammonia-based pretreatments on lignocellulose.
Original language | English |
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Pages (from-to) | 204-218 |
Number of pages | 15 |
Journal | Green Chemistry |
Volume | 22 |
Issue number | 1 |
DOIs | |
State | Published - 2020 |
Funding
SPSC acknowledges support from the ORAU 2016 Ralph E. Powe Award, ORNL Neutron Sciences User Facility, US National Science Foundation CBET awards (1604421 and 1846797), Rutgers Global Grant, Rutgers Division of Continuing Studies, Rutgers School of Engineering, and the Great Lakes Bioenergy Research Center (DOE BER Office of Science DE-FC02-07ER64494). MD and SANS studies on Bio-SANS were supported by the Office of Biological and Environmental Research (OBER) funded Center for Structural Molecular Biology (CSMB) under contract FWP ERKP291 and the Bio-Fuels Science Focus Area under contract FWP ERKP752, using the High Flux Isotope Reactor supported by the Office of Basic Energy Sciences (BES), U. S. Department of Energy (DOE). SR and CZ acknowledge support from University Grants Commission of India (Raman Fellowship Program) and China Scholarship Council, respectively, to support their one-year postdoctoral research work at SPSC’s lab at Rutgers University. Lastly, we are very grateful to Benjamin Esposito and Jia-Mei Hong from SPSC’s Rutgers research group for their critical experimental contributions to the project. This manuscript has been co-authored by UT-Battelle, LLC, under Contract No. DE-AC05-00OR22725 with the U.S. Department of Energy. The United States Government retains and the publisher, by accepting the article for publication, acknowledges that the United States Government retains a non-exclusive, paid-up, irrevocable, world-wide license to publish or reproduce the published form of this manuscript, or allow others to do so, for United States Government purposes. The Department of Energy will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan (http://energy.gov/downloads/ doe-public-access-plan).
Funders | Funder number |
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UT-Battelle | |
National Science Foundation | 1604421, 1846797 |
Oak Ridge Associated Universities |