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The conventional fractionation of lignocellulose into cellulose, hemicellulose, and lignin was generally carried out at high temperatures and under highly acidic conditions owing to the rigid matrix of lignocellulose and crystallinity of cellulose, causing the degradation of carbohydrates and condensation of lignin, thus hindering their value-added utilization. In this study, a stepwise fractionation method was proposed in which microwave-assisted fractionation of hemicellulose under mild conditions contributed to 81.9% of xylose yield; then, the cellulose part solid was rapidly dissolved in LiBr molten salt hydrate (LiBr-MSH) solution, followed by a filtration process to isolate lignin solid. It was found that the removal of hemicellulose provided more pores for the next dissolution of cellulose, and LiBr-MSH caused the cleavage of the hydrogen bonds of cellulose. Consequently, the cellulose part solid was rapidly dissolved in LiBr-MSH. The results showed that under the optimal fractionation conditions, 78.0% yield of glucan oligomers and 89.7% purity of noncondensed lignin were obtained from cellulose fractionation and filtration, respectively. A high β-O-4 bond content close to 87.3% of the theoretical maximum yield was detected in the obtained lignin, indicating that most β-O-4 bond structure of lignin was well preserved. Additionally, the isolated lignin can be selectively depolymerized into aromatic monomers with a high yield of 20.4%, which is 74.2% of the theoretical maximum yield. [ABSTRACT FROM AUTHOR]

Selective production of glucose from cellulose in a molten salt hydrate (MSH) shows high efficiency but the separation of glucose is still challenging. To address this issue, we proposed a stepwise method, where cellulose was first hydrolyzed into glucan oligomers and separated via anti-solvent precipitation, followed by being hydrolyzed into glucose under mild conditions. For potential industrial applications, using raw biomass as a substrate is more attractive due to its commercial advantages. However, directly hydrolyzing raw corn stover in an MSH resulted in a low glucan oligomer yield and sugar concentration, together with insufficient separation efficiency. This work demonstrated that the generation of acetic acid during hemicellulose hydrolysis is the critical factor affecting glucan oligomer selectivity. To address this issue, a pre-extraction method using auto-hydrolysis was proposed to remove hemicellulose before MSH hydrolysis. After pre-extraction, the obtained glucan oligomer yield could be enhanced from 59.9% to 79.5%, with the separation efficiency increased from 53.7% to 80.6% by methanol precipitation. Besides, increasing the raw corn stover concentration led to an increase in acetic acid and resulted in glucan oligomer degradation. However, after removing hemicellulose, the concentration of glucan oligomers could be significantly enhanced from less than 72.1 to 121.5 mg mL−1. Thus, pre-extraction of hemicellulose followed by MSH hydrolysis provides a potential application for directly producing glucan oligomers from raw biomass with improved yield and separation efficiency. [ABSTRACT FROM AUTHOR]

Molten salt hydrate (MSH) is unique in cellulose dissolution and in one-pot conversion of crystalline cellulose into 5-hydroxymethylfurfural (5-HMF). However, low yield of 5-HMF was obtained using raw biomass substrate in MSHs. Herein, we investigated conversion of raw biomass towards HMF using MSHs. We showed that the release of acetic acid from hemicellulose degradation in MSH is a key to influence the yield of 5-HMF. Thus, an autohydrolysis pretreatment method was proposed to remove hemicellulose before conversion of cellulose into 5-HMF. After being pretreated at 180 °C for 40 min, hemicellulose was removed from biomass with 91.8% yield of cellulose remained in solid part. By eliminating the negative effect of acetic acid, 5-HMF yield was significantly improved from 40.9% to 64.6%, together with 9.3% yield of glucose for cellulose conversion in MSH/acetone at 180 °C for 20 min. [ABSTRACT FROM AUTHOR]

A two-stage process was evaluated to increase sugar recovery. Firstly, corn stover was treated with dilute hydrochloric acid to recover the xylose, and then the residue was subjected to a wet-milling pretreatment. Dilute hydrochloric acid showed a high xylose recovery during the first stage. The optimal condition was 120 °C and 40 min for 0.7 wt% dilute hydrochloric acid pretreatment followed by wet-milling pretreatment for 15 min. The xylose and glucose yield were 81.0% and 64.0%, respectively, with a cellulase dosage at 3 FPU/g of substrate. This two-stage process was effective on account of the removal of hemicelluloses in the first stage and the delamination of cell wall in the second stage, increasing the possibility of adsorption of cellulose to enzymes, and resulting in a high sugar recovery with a very low enzyme loading. [ABSTRACT FROM AUTHOR]

Molten salt hydrates (MSHs) are remarkable in breaking through the recalcitrant structure of microcrystalline cellulose and raw biomass. After being pretreated in 60 wt% LiBr at 130 °C for 2 h, cellulose crystallinity as well as degree of polymerization (DP) decreased. It was found that 91.3% yield of pretreated cellulose was removed from MSHs by filteration followed by being hydrolyzed into glucose with a high yield of 75.3% by dilute acid under mild reaction conditions. The pretreatment process also works on raw corn stover hydrolysis. After being pretreated at 100 °C for 5 h, 88.4% yield of cellulose in biomass was recovered and can be hydrolyzed into 54.9% yield of glucose with dilute acid. It was found that the cellulose in corn stover can be easier degraded compared with microcrystalline cellulose during MSHs pretreatment, which dues to the formation of acetic acid from hemicellulose hydrolysis. The proposed pretreatment technique presents a promising potential for glucose production from biomass in a commercial way. Unlabelled Image • MSHs pretreatment effectively decreased cellulose crystallinity and DP. • After being pretreated at 130°C for 2 h, 91.3% of cellulose was removed from MSHs via filtration. • Enhanced glucose yield of 75.3% was obtained from pretreated cellulose hydrolysis at mild condition. • 88.4% cellulose recovery and 54.9% glucose yield were obtained from MSHs pretreatment and hydrolysis, respectively. [ABSTRACT FROM AUTHOR]

With the aim to enhance the direct conversion of raw corn stover into furfural, a promising approach was proposed employing a novel heterogeneous strong acid catalyst (SC-CaC t -700) in different solvents. The novel catalyst was characterized by elemental analysis, N 2 adsorption-desorption, FT-IR, XPS, TEM and SEM. The developed catalytic system demonstrated superior efficacy for furfural production from raw corn stover. The effects of reaction temperature, residence time, catalyst loading, substrate concentration and solvent were investigated and optimized. 93% furfural yield was obtained from 150 mg corn stover at 200 °C in 100 min using 45 mg catalyst in γ-valerolactone (GVL). In comparison, 51.5% furfural yield was achieved in aqueous media under the same conditions (200 °C, 5 h, and 45 mg catalyst), which is of great industrial interest. Furfural was obtained from both hemicelluloses and cellulose in corn stover, which demonstrated a promising routine to make the full use of biomass. [ABSTRACT FROM AUTHOR]

P-toluene sulfonic acid (PTSA) was utilized to pretreat corn stover. Changes in morphology and structure of untreated and pretreated samples were analyzed by ESEM, TEM, BET, XRD and SXT. The characterization results demonstrated that PTSA pretreatment could markedly improve cellulase accessibility to cellulose because of the removal of lignin and hemicellulose simultaneously. The maximum glucose yield (67.2%) with an enzyme loading of 5FPU•g−1 substrate was achieved after the sample was the pretreated at 80 °C for 10 min with 71.0 wt% PTSA. P-toluene sulfonic acid pretreatment was a valid method to improve the enzymatic hydrolysis performance of cellulose in corn stover at low reaction temperature with a short reaction time. • PTSA pretreatment can remove lignin and hemicellulose simultaneously under mild condition. • P-toluene sulfonic acid pretreatment was an effective pretreatment process. • 67.2% of glucose yield was achieved at a low enzyme loading of 5FPU·g−1 substrate. [ABSTRACT FROM AUTHOR]