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Atmospheric pressure nonthermal plasma treatment can be a novel, green and low energy method to convert biomass to biobased chemicals. The unique physiochemistry of plasma discharge enables reactions within biomass that otherwise could not possibly occur under traditional conditions. In this study, we present a simple method of producing a high yield of levoglucosan from cellulose without using any catalysts, chemicals, solvents or vacuum, but by using plasma treatment to control the depolymerization mechanism of cellulose. Cellulose was first pretreated in a dielectric barrier discharge reactor operating in ambient air or argon for 10–60 s, followed by pyrolysis at 350–450 °C to produce up to 78.6% of levoglucosan. Without the plasma pretreatment, the maximum yield of levoglucosan from cellulose pyrolysis was 58.2%. The results of this study showed that the plasma pretreatment led to homolytic cleavage of glycosidic bonds. The resulting free radicals were then trapped within the cellulose structure when the plasma discharge stopped, allowing subsequent pyrolysis of the plasma-pretreated cellulose to proceed through a radical-based mechanism. The present results also revealed that although the radical-based mechanism is highly selective to levoglucosan formation, this pathway is usually discouraged when the untreated cellulose is pyrolyzed due to the high energy barrier for homolytic cleavage. Initiating homolytic cleavage during the plasma pretreatment also helped the pretreated cellulose to produce higher yields of levoglucosan using lower pyrolysis temperatures. At 375 °C, the levoglucosan yield was only 53.2% for the untreated cellulose, whereas the yield reached 77.6% for the argon-plasma pretreated cellulose.
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This content will become publicly available on November 16, 2025
Programmable C−N Bond Formation through Radical‐Mediated Chemistry in Plasma‐Microdroplet Fusion
Non‐thermal plasma discharge produced in the wake of charged microdroplets is found to facilitate catalyst‐free radical mediated hydrazine cross‐coupling reactions without the use of external light source, heat, precious metal complex, or trapping agents. A plasma‐microdroplet fusion platform is utilized for introduction of hydrazine reagent that undergoes homolytic cleavage forming radical intermediate species. The non‐thermal plasma discharge that causes the cleavage originates from a chemically etched silica capillary. The coupling of the radical intermediates gives various products. Plasma‐microdroplet fusion occurs online in a programmable reaction platform allowing direct process optimization and product validation via mass spectrometry. The platform is applied herein with a variety of hydrazine substrates, enabling i) self‐coupling to form secondary amines with identical N‐substitutions, ii) cross‐coupling to afford secondary amine with different N‐substituents, iii) cross‐coupling followed by in situ dehydrogenation to give the corresponding aryl‐aldimines with two unique N‐substitutions, and iv) cascade heterocyclic carbazole derivatives formation. These unique reactions were made possible in the charged microdroplet environment through our ability to program conditions such as reagent concentration (i. e., flow rate), microdroplet reactivity (i. e., presence or absence of plasma), and reaction timescale (i. e., operational mode of the source). The selected program is implemented in a co‐axial spray format, which is found to be advantageous over the conventional one‐pot single emitter electrospray‐based microdroplet reactions.
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- Award ID(s):
- 2150102
- PAR ID:
- 10563068
- Publisher / Repository:
- Wiley
- Date Published:
- Journal Name:
- Angewandte Chemie International Edition
- ISSN:
- 1433-7851
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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