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      A mild biomass pretreatment using γ-valerolactone for concentrated sugar production

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          Abstract

          Here we report that γ-valerolactone (GVL), a biomass-derived solvent, can be used to facilitate the mild pretreatment of lignocellulosic biomass.

          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 2SO 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 the original glucan and 96% of the original xylan could be recovered after pretreatment. The pretreated substrate was quantitatively converted to sugars (99% and 100% total glucose and xylose yield) with an enzyme loading of 15 FPU g −1 glucan. These digestibilities were three times higher than those obtained when using other organic solvents such as tetrahydrofuran or ethanol, and 20 times higher than when pure water was used during pretreatment. Over 99.5% of GVL could be recovered by liquid–CO 2 extraction of the pretreated slurries while removing less than 1% of the sugars. This approach produced pretreatment slurries that could easily undergo high-solids (30% w/v) enzymatic hydrolysis without any substrate washing or drying. We obtained glucose and xylose yields of up to 90% and 97%, respectively, and generated sugar streams with sugar concentrations up to 182 g L −1.

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          Bioconversion of lignocellulose: inhibitors and detoxification

          Bioconversion of lignocellulose by microbial fermentation is typically preceded by an acidic thermochemical pretreatment step designed to facilitate enzymatic hydrolysis of cellulose. Substances formed during the pretreatment of the lignocellulosic feedstock inhibit enzymatic hydrolysis as well as microbial fermentation steps. This review focuses on inhibitors from lignocellulosic feedstocks and how conditioning of slurries and hydrolysates can be used to alleviate inhibition problems. Novel developments in the area include chemical in-situ detoxification by using reducing agents, and methods that improve the performance of both enzymatic and microbial biocatalysts.
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            Lignocellulosic biomass to bioethanol, a comprehensive review with a focus on pretreatment

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              Organosolv pretreatment of lignocellulosic biomass for enzymatic hydrolysis.

              Production of ethanol by bioconversion of lignocellulosic biomass has attracted much interest in recent years. However, the pretreatment process for increasing the enzymatic digestibility of cellulose has become a key step in commercialized production of cellulosic ethanol. During the last decades, many pretreatment processes have been developed for decreasing the biomass recalcitrance, but only a few of them seem to be promising. From the point of view for integrated utilization of lignocellulosic biomass, organosolv pretreatment provides a pathway for biorefining of biomass. This review presents the progress of organosolv pretreatment of lignocellulosic biomass in recent decades, especially on alcohol, organic acid, organic peracid and acetone pretreatments, and corresponding action mechanisms. Evaluation and prospect of organosolv pretreatment were performed. Finally, some recommendations for future investigation of this pretreatment method were given.

                Author and article information

                Journal
                GRCHFJ
                Green Chemistry
                Green Chem.
                Royal Society of Chemistry (RSC)
                1463-9262
                1463-9270
                2016
                2016
                : 18
                : 4
                : 937-943
                Article
                10.1039/C5GC02489G
                2d5a1ff3-0733-4a35-8d8f-301531c74db8
                © 2016
                History

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