2021
DOI: 10.1246/cl.200873
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Effective Lignin Utilization Strategy: Major Depolymerization Technologies, Purification Process and Production of Valuable Material

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Cited by 7 publications
(3 citation statements)
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“…The structure of lignin oen varies depending on the plant species and its environment. 20 Lignin is a complex three-dimensional phenolic polymer formed by phenyl propane units linked by C-C or C-O-C bonds, which contains a variety of reactive functional groups, such as carbonyl, carboxyl and hydroxyl groups so that lignin has phenolic properties. By density ooding theory (DFT) analysis, the magnitude of the bond dissociation energy in lignin is ranked as 21 During lignin treatment, the bonds in which the chemical bonds require the least energy to break are the a-O-4 and b-O-4 bonds, respectively, which break easily and produce hydroxyl groups.…”
Section: Preparation Of Lcasmentioning
confidence: 99%
“…The structure of lignin oen varies depending on the plant species and its environment. 20 Lignin is a complex three-dimensional phenolic polymer formed by phenyl propane units linked by C-C or C-O-C bonds, which contains a variety of reactive functional groups, such as carbonyl, carboxyl and hydroxyl groups so that lignin has phenolic properties. By density ooding theory (DFT) analysis, the magnitude of the bond dissociation energy in lignin is ranked as 21 During lignin treatment, the bonds in which the chemical bonds require the least energy to break are the a-O-4 and b-O-4 bonds, respectively, which break easily and produce hydroxyl groups.…”
Section: Preparation Of Lcasmentioning
confidence: 99%
“…The "lignin-first" biorefining concept, termed reductive catalytic fractionation (RCF) or catalytic upstream biorefining (CUB), [189,190] represents a forward-looking methodology initiating with lignocellulose. This strategy affords the notable benefit of accomplishing a comprehensive separation of carbohydrate and lignin fractions under a reductive environment.…”
Section: Lignocellulose As Substratementioning
confidence: 99%
“…Here, multi-functional cinnamate-like monomers with unsaturated double bonds were synthesized using vanillin, a product of oxidative degradation of lignin, which is also commercially available; 3,4-dihydroxybenzaldehyde, can be obtained via oxidative degradation followed by a demethylation process; and glycerol, a byproduct of the biodiesel production process. [33][34][35][36][37] The critical properties, such as the extent of crosslinking, decrosslinking, glass transition temperatures and their effect on adhesive lap shear strength, were analyzed for six different structures with tri-, tetra-, and hexa-functional core and catechol, methoxy, propyl, and pentyl side chain attachments. We hypothesized that, due to the inherent photoreversible properties and the high tunability of the structures, we could potentially make the functional polymers work as reusable adhesives.…”
Section: Introductionmentioning
confidence: 99%