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      Protected lignin biorefining through cyclic extraction: gaining fundamental insights into the tuneable properties of lignin by chemometrics

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          Abstract

          An integrated lignin biorefinery process was studied by chemometrics. A regime for structurally preserved lignins with tuneable properties was identified.

          Abstract

          Lignin is a renewable source of aromatics with great potential as a substitute for fossil-based phenolic compounds that are used in several material applications. However, the available technical lignins are heterogenic and still structurally not fully understood. This presents hurdles for studies focused on gaining fundamental insights into how materials properties are related to the molecular structure of lignin. In the present study, a novel cyclic extraction process for lignin is more deeply studied to investigate the potential to tailor the chemical and physical properties of lignin. For this purpose, a design of experiment (DoE) approach was adopted as a tool to investigate the effect on the lignin properties of the selected parameters by including linear, quadratic and interaction effects in a multiple linear regression (MLR) model. Molecular characterization techniques included 1D and 2D NMR, SEC and DSC. It was clearly demonstrated that the chemical and physical properties of lignin could be tuned for the cyclic process using the DoE approach, while preserving 66–82% of the commonly known lignin inter-units, substantiating that the cyclic extraction approach offered a decent to excellent level of protection to inter-units when compared to benchmark organosolv and kraft lignin. By manipulation of the extraction conditions, the β-O-4′ content can be tuned between 20 and 35% simultaneously with the content of phenolic and aliphatic hydroxyls. Finally, DSC studies showed T gs in the range of 150–185 °C which are discussed with respect to the molecular properties of the analysed lignin. Overall, to advance efforts in lignin valorization, a green process to produce a library of well-characterized lignins, tailored with respect to chemical and physical properties by process conditions, is presented.

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          Most cited references43

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          Formaldehyde stabilization facilitates lignin monomer production during biomass depolymerization

          Practical, high-yield lignin depolymerization methods could greatly increase biorefinery productivity and profitability. However, development of these methods is limited by the presence of interunit carbon-carbon bonds within native lignin, and further by formation of such linkages during lignin extraction. We report that adding formaldehyde during biomass pretreatment produces a soluble lignin fraction that can be converted to guaiacyl and syringyl monomers at near theoretical yields during subsequent hydrogenolysis (47 mole % of Klason lignin for beech and 78 mole % for a high-syringyl transgenic poplar). These yields were three to seven times those obtained without formaldehyde, which prevented lignin condensation by forming 1,3-dioxane structures with lignin side-chain hydroxyl groups. By depolymerizing cellulose, hemicelluloses, and lignin separately, monomer yields were between 76 and 90 mole % for these three major biomass fractions.
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            Some New Three Level Designs for the Study of Quantitative Variables

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              Review of current and future softwood kraft lignin process chemistry

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                Author and article information

                Contributors
                (View ORCID Profile)
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                Journal
                GRCHFJ
                Green Chemistry
                Green Chem.
                Royal Society of Chemistry (RSC)
                1463-9262
                1463-9270
                February 07 2022
                2022
                : 24
                : 3
                : 1211-1223
                Affiliations
                [1 ]Wallenberg Wood Science Center, Department of Fiber and Polymer Technology, School of Engineering Sciences in Chemistry, Biotechnology and Health, Royal Institute of Technology, KTH Teknikringen 56-58, 100 44 Stockholm, Sweden
                [2 ]Division of Wood Chemistry and Pulp Technology, Department of Fiber and Polymer Technology, School of Engineering Sciences in Chemistry, Biotechnology and Health, Royal Institute of Technology, KTH Teknikringen 56-58, 100 44 Stockholm, Sweden
                Article
                10.1039/D1GC04171A
                3a62b8d5-f5fd-4636-ac1c-9864fde28c81
                © 2022

                http://creativecommons.org/licenses/by/3.0/

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