Abstract:Here we report that γ-valerolactone (GVL), a biomass-derived solvent, can be used to facilitate the mild pretreatment of lignocellulosic biomass. An 80% GVL, 20% water solvent system was used to pretreat hardwood at the mild temperature of 120°C with an acid loading of 75 mM H 2 SO 4 . Up to 80% of original lignin was removed with 96-99% of original cellulose retained in the pretreated substrates. The use of a mild temperature and low acid concentrations caused negligible degradation of sugars. Up to 99% of th… Show more
“…The first analysis considers six different pretreatment concepts using only beech wood as feedstock: dilute acid (DA), ionic liquid (IL), Kraft, liquid hot water (LHW), a one‐phasic organosolv (OS) and a two‐phasic organosolv (Organocat (OC)) (cf. supplementary material File S1 for selection of references).…”
“…The first analysis considers six different pretreatment concepts using only beech wood as feedstock: dilute acid (DA), ionic liquid (IL), Kraft, liquid hot water (LHW), a one‐phasic organosolv (OS) and a two‐phasic organosolv (Organocat (OC)) (cf. supplementary material File S1 for selection of references).…”
“…Another option that has been revitalized is pretreatment with ionic liquids to fractionate biomass at mild reaction conditions [23, 141,142]. The use of gamma-valerolactone (GVL) was introduced more recently to remove lignin from biomass and promote its deconstruction [143]. Most recently, adding tetrahydrofuran (THF) in solution with water significantly enhanced dilute acid deconstruction of biomass at lower reaction temperatures by simultaneously promoting high sugar recovery from hemicellulose into the liquid, producing highly digestible glucan-rich solids, and extracting lignin by precipitation from solution after removing low boiling tetrahydrofuran (THF) [144].…”
Section: Pretreatment Prior To Enzymatic Hydrolysismentioning
“…Notably, liquid CO 2 was used to extract over 99% of GVL from the reaction media of several biomass conversion processes. 59,60 After its addition, a CO 2 -expanded phase was created with GVL, which was no longer miscible with water. This lead to the production of a GVL phase and a concentrated aqueous phase containing over 90% of the carbohydrates produced from biomass which allowed for an easy recovery of GVL.…”
Section: Physical Processes Employing High-pressure Co 2 or Co 2 -H 2mentioning
confidence: 99%
“…This lead to the production of a GVL phase and a concentrated aqueous phase containing over 90% of the carbohydrates produced from biomass which allowed for an easy recovery of GVL. [59][60][61][62] Another important approach developed for biorefinery processes has been the use of CO 2 explosion to disrupt raw cellulosic substrates. [63][64][65][66][67] The instantaneous release of CO 2 at high pressure promotes the disruption of the cellulosic structure and leads to increases in the accessible surface area of the substrate used for further hydrolysis.…”
Section: Physical Processes Employing High-pressure Co 2 or Co 2 -H 2mentioning
Biomass is an attractive source of renewable carbon-based fuels and chemicals and their production is envisaged within the framework of integrated biorefineries. Multiple research efforts to make biorefineries more economically competitive and sustainable are ongoing. In this context the use of high-pressure CO2 and CO2/H2O mixtures for biomass conversion is especially attractive. These mixtures are cheap, renewable, environmentally benign and allow tuning of various processing parameters by varying temperature, pressure and CO2 loading. This chapter presents a broad introduction of the principal processes and conversion routes being considered within biorefineries, and how high-pressure CO2 and CO2/H2O mixtures could help address certain challenges associated with biomass conversion. Some of the principle advantages associated with high-pressure CO2 and CO2/H2O mixtures that we highlight here are their abilities to act as green substitutes for unsustainable solvents, to enhance acid-catalysed reaction rates by in situ carbonic acid formation, to reduce mass transfer-limitations, and to increase access to substrates and catalysts. We discuss these advantages in the context of the trade-offs associated with implementing large-scale high-pressure systems including safety concerns and increased capital costs. With this introduction, we highlight both the principal benefits and challenges associated with the use of high-pressure CO2 and CO2/H2O mixtures, which are further detailed in subsequent chapters.
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