Shao-Long Sun

Recent Advances in Characterization of Lignin Polymer by Solution-State Nuclear Magnetic Resonance (NMR) Methodology

The demand for efficient utilization of biomass induces a detailed analysis of the fundamental chemical structures of biomass, especially the complex structures of lignin polymers, which have long been recognized for their negative impact on biorefinery. Traditionally, it has been attempted to reveal the complicated and heterogeneous structure of lignin by a series of chemical analyses, such as thioacidolysis (TA), nitrobenzene oxidation (NBO), and derivatization followed by reductive cleavage (DFRC). Recent advances in nuclear magnetic resonance (NMR) technology undoubtedly have made solution-state NMR become the most widely used technique in structural characterization of lignin due to its versatility in illustrating structural features and structural transformations of lignin polymers. As one of the most promising diagnostic tools, NMR provides unambiguous evidence for specific structures as well as quantitative structural information. The recent advances in two-dimensional solution-state NMR techniques for structural analysis of lignin in isolated and whole cell wall states (in situ), as well as their applications are reviewed.

The role of pretreatment in improving the enzymatic hydrolysis of lignocellulosic materials.

Lignocellulosic materials are among the most promising alternative energy resources that can be utilized to produce cellulosic ethanol. However, the physical and chemical structure of lignocellulosic materials forms strong native recalcitrance and results in relatively low yield of ethanol from raw lignocellulosic materials. An appropriate pretreatment method is required to overcome this recalcitrance. For decades various pretreatment processes have been developed to improve the digestibility of lignocellulosic biomass. Each pretreatment process has a different specificity on altering the physical and chemical structure of lignocellulosic materials. In this paper, the chemical structure of lignocellulosic biomass and factors likely affect the digestibility of lignocellulosic materials are discussed, and then an overview about the most important pretreatment processes available are provided. In particular, the combined pretreatment strategies are reviewed for improving the enzymatic hydrolysis of lignocellulose and realizing the comprehensive utilization of lignocellulosic materials.

Understanding the chemical transformations of lignin during ionic liquid pretreatment

Unveiling the fundamental chemistry of lignin under ionic liquid (IL) pretreatment will facilitate the understanding of biomass recalcitrance involved in pretreatment processes. To examine in greater detail the chemical transformations of lignin under different IL pretreatment conditions without competing reactions from plant polysaccharides, the IL pretreatment of the isolated poplar alkaline lignin (hardwood lignin) under varying IL pretreatment conditions (i.e., 110–170 °C, 1–16 hours) was performed in an appropriate manner. The structural transformations of the lignin have been investigated by elemental analysis, 2D-HSQC spectra, quantitative 13C-NMR spectra, 31P NMR, and GPC analysis. Results revealed that a decrease of aliphatic OH and an increase in phenolic hydroxyl groups occurred in lignin as the pretreatment proceeded. The increased phenolic OH was mainly as a result of cleavage of β-O-4′ linkages, while the reduced aliphatic OH is probably attributed to the dehydration reaction. The cleavage of β-O-4′ linkages, degradation of β–β′ and β-5′ linkages obviously happened at high temperatures and resulted in the decrease of molecular weights. In addition, IL pretreatment selectively degraded the G-type lignin fractions and the condensation reaction took place more easily at S units than G units. Moreover, the demethoxylation preferentially occurred in G units, especially at higher temperatures. It is believed that investigating the fundamental chemistry of lignin during IL pretreatments would be beneficial to optimize and control the pretreatment process.

Quantitative Structures and Thermal Properties of Birch Lignins after Ionic Liquid Pretreatment

The use of ionic liquid (IL) in biomass pretreatment has received considerable attention recently because of its effectiveness in decreasing biomass recalcitrance to subsequent enzymatic hydrolysis. To understand the structural changes of lignin after pretreatment and enzymatic hydrolysis process, ionic liquid lignin (ILL) and subsequent residual lignin (RL) were sequentially isolated from ball-milled birch wood. The quantitative structural features of ILL and RL were compared with the corresponding cellulolytic enzyme lignin (CEL) by nondestructive techniques (e.g., FTIR, GPC, quantitative (13)C, 2D and (31)P NMR). The IL pretreatment caused structural modifications of lignin (cleavage of β-O-4 ether linkages and formation of condensed structures). In addition, lignin fragments with lower S/G ratios were initially extracted, whereas the subsequently extracted lignin is rich in syringyl unit. Moreover, the maximum decomposition temperature (T(M)) was increased in the order ILL < RL < CEL, which was related to the corresponding β-O-4 ether linkage content and molecular weight (M(w)). On the basis of the results observed, a possible separation mechanism of IL lignin was proposed.

Structural elucidation of lignin polymers of Eucalyptus chips during organosolv pretreatment and extended delignification.

Effective delignification of lignocelluloses is a very important to guarantee the economic feasibility of organosolv-based biorefinery. Eucalyptus chips were successively subjected to organosolv pretreatment (AEOP) and extended delignification (ED) process in the present study. The effects of delignification processes were scientifically evaluated by component analysis, SEM, and CP-MAS NMR techniques. It was found that the integrated process of organosolv pretreatment and subsequent delignification resulted in an effective delignification. The fundamental chemistry of the lignin obtained after these processes was thoroughly investigated by FT-IR, multidimensional NMR ((31)P-, (13)C-, and 2D-HSQC NMR), and GPC techniques. It was observed that an extensive cleavage of aryl ether linkages, ethoxylation, and some condensation reactions occurred in AEOP process, while α-oxidation mainly took place in alkaline hydrogen peroxide (AHP) process. It is believed that better understanding the fundamental chemistry of lignin facilitates the optimization of the delignification process. More importantly, well-defined of lignin polymers will facilitate their value-added applications in current and future biorefineries.

Successive alkali extraction and structural characterization of hemicelluloses from sweet sorghum stem

Sweet sorghum stem was successively extracted with water at 90 °C, 0.3, 0.6, 1.0, 1.5, and 2.0% KOH aqueous solution, and 60% ethanol containing 2.5% KOH at 75 °C for 3 h, yielding 76.3% of the original hemicelluloses. Chemical composition and structural characterization of the seven hemicellulosic fractions obtained were comparatively investigated by a combination of HPAEC, GPC, FT-IR, (1)H-, (13)C-, HSQC NMR and TGA techniques. According to the spectral analysis, hemicelluloses from sweet sorghum stem are assumed to L-arabino-4-O-methyl-D-glucurono-D-xylan. In addition, the higher molecular weights of hemicelluloses resulted in a higher thermal stability of the samples. The present study suggests that successive alkali extraction is a promising approach for fractionation of hemicelluloses from sweet sorghum stem and to prepare hemicellulosic polymers with different branching and molecular weights.

Structural elucidation of whole lignin from Eucalyptus based on preswelling and enzymatic hydrolysis

The structural elucidation of whole lignin in the plant cell wall is extremely important for providing a representative lignin to understand the molecular characteristics of lignin in plants, and develop lignin-based polymers and green chemicals under the current biorefinery scenario. However, research in this area still lack methodologies for effectively isolating whole lignin from the plant cell wall. In this study, an effective method based on mild alkaline preswollen (4% NaOH, 25 °C, 24 h) and enzymatic hydrolysis for the isolation of “swollen residual enzyme lignin, SREL” from Eucalyptus wood was proposed. SREL was investigated as compared to the corresponding cellulolytic enzyme lignin (CEL) and alkali lignin (AL). Observably, the yield of SREL (95%) was significantly higher than that of the corresponding CEL (20%) and AL (12%). The isolated lignin has been comparatively investigated by a combination of elemental analysis, 2D HSQC NMR, 31P-NMR, analytical pyrolysis, and GPC techniques. The major lignin linkages (β-O-4′, β–β′, β-5′, etc.) were thoroughly assigned and the frequencies of the major lignin linkages were quantitatively compared. Further experiments demonstrated that a transformation from cellulose I to cellulose II occurred during alkaline preswelling of the ball-milled Eucalyptus wood, which resulted in the efficient enzymatic hydrolysis of the substrates, thus yielding a representative lignin sample (SREL). However, the alkaline preswelling treatment has little effect on the lignin structures (typical substructures); it only tends to yield syringyl-rich lignin macromolecules as compared to CEL. Furthermore, the effective method gives us a panoramic image to understand the intrinsic structural features of whole lignin from other lignocellulosic biomasses and helps to develop more effective plant deconstruction or depolymerization strategies in the current biorefinery and catalytic conversion process.

Assessment of integrated process based on hydrothermal and alkaline treatments for enzymatic saccharification of sweet sorghum stems.

In this study, sweet sorghum stem was subjected to hydrothermal pretreatment (HTP) and alkaline post-treatment to enhance its saccharification ratio by reducing its recalcitrance. The results showed that the HTP (110-210°C, 0.5-2.0h) significantly degraded hemicelluloses, and the pretreatment at the temperature higher than 190°C led to the partial degradation of the cellulose. As compared to the sole HTP, the integrated process removed most of lignin and hemicelluloses, which incurred a higher cellulose saccharification ratio. Under an optimum condition evaluated (HTP at 170°C for 0.5h and subsequent 2% NaOH treatment), 77.5% saccharification ratio was achieved, which was 1.8, 2.0 and 5.5 times as compared to the only HTP pretreated substrates, alkaline treated substrates alone and the raw material without pretreatment, respectively. Clearly, the integrated process can be considered as a promising approach to achieve an efficient conversion of lignocellulose to fermentable glucose.

Why to synthesize vaterite polymorph of calcium carbonate on the cellulose matrix via sonochemistry process

Vaterite is an important biomedical material due to its features such as high specific surface area, high solubility, high dispersion, and small specific gravity. The purposes of this article were to explore the growth mechanism of vaterite on the cellulose matrix via sonochmistry process. In the work reported herein, the influences of experimental parameters on the polymorph of calcium carbonate were investigated in detail. The calcium carbonate crystals on the cellulose matrix were characterized by means of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). Experimental results revealed that all the reactants, solvent, and synthesis method played an important role in the polymorph of calcium carbonate. The pure phase of vaterite polymorph was obtained using Na2CO3 as reactant in ethylene glycol on the cellulose matrix via sonochmistry process. Based on the experimental results, one can conclude that the synthesis of vaterite polymorph is a system process.

Structural Elucidation of Sorghum Lignins from an Integrated Biorefinery Process Based on Hydrothermal and Alkaline Treatments

An integrated process based on hydrothermal pretreatment (HTP) (i.e., 110-230 °C, 0.5-2.0 h) and alkaline post-treatment (2% NaOH at 90 °C for 2.0 h) has been performed for the production of xylooligosaccharide, lignin, and digestible substrate from sweet sorghum stems. The yield, purity, dissociation mechanisms, structural features, and structural transformations of alkali lignins obtained from the integrated process were investigated. It was found that the HTP process facilitated the subsequent alkaline delignification, releasing lignin with the highest yield (79.3%) and purity from the HTP residue obtained at 190 °C for 0.5 h. All of the results indicated that the cleavage of the β-O-4 linkages and degradation of β-β and β-5 linkages occurred under the harsh HTP conditions. Depolymerization and condensation reactions simultaneously occurred at higher temperatures (≥ 170 °C). Moreover, the thermostability of lignin was positively related to its molecular weight, but was also affected by the inherent structures, such as β-O-4 linkages and condensed units. These findings will enhance the understanding of structural transformations of the lignins during the integrated process and maximize the potential utilizations of the lignins in a current biorefinery process.