Lignin-carbohydrate Complexes Research Articles

Durable Biopolymer Films From Lignin-Carbohydrate Complex Derived From a Pulp Mill Side Stream

Valorization of side streams offers novel types of raw materials to complement or replace synthetic and food-based alternatives in materials science, increasing profitability and decreasing the environmental impacts of biorefineries. Lignocellulose biomass contains lignin and carbohydrates that are covalently linked into lignin-carbohydrate complexes (LCCs). In biomass fractionation processes, these complexes are conventionally considered as waste, which hinders the biomass fractionation process, and they may solubilize into aqueous effluents. This study presents how LCCs, derived from pulp mill effluent, can be turned into valuable biopolymers for industrial polymer film applications. Free-standing composite films containing hydroxyethyl cellulose (HEC) and LCCs with varying molar mass, charge density and lignin/hemicellulose ratio were prepared to study the effect of LCC amount on mechanical properties and oxygen permeability. Increasing the LCC content increased the yield point and Young’s modulus of the films. Breaking strain measurements revealed a non-linear correlation with the LCC concentration for the samples with higher lignin than hemicellulose content. The addition of LCC enhanced oxygen barrier properties of HEC films significantly even at high relative humidity. The present research demonstrates how a currently underutilized fraction of the biorefinery side stream has the potential to be valorized as a biopolymer in industrial applications, for example as a barrier film for paper and board packaging.

Chlorine dioxide oxidation of hemicellulose from alkaline hydrolysate bagasse to remove lignin unit in lignin-carbohydrate complex

Owing to the existence of lignin-carbohydrate complex (LCC) linkages, the extracted hemicellulose contains lignin, which is difficult to remove. Chlorine dioxide selectively oxidizes lignin without reacting with carbohydrates. In this study, chlorine dioxide was used to remove lignin from the hemicellulose sample. Ion chromatography and 2D-HSQC NMR were used to observe the changes in the LCC. After chlorine dioxide treatment, acid-insoluble lignin was largely degraded, with a removal rate reaching 68%. Furthermore, the 2D-HSQC NMR spectrum showed that guaiacyl (G) lignin underwent dramatic degradation and degradation of syringyl (S) lignin was also obvious. Phenyl glycoside-type LC linkages were also largely degraded. Moreover, the sugar composition and structure of the hemicellulose did not change significantly. This suggests that it is feasible to remove lignin from LCCs through oxidation of hemicellulose using chlorine dioxide. Meanwhile, hemicellulose with high molecular weight and high purity can be obtained by this method.

Structural changes of lignin-carbohydrate complexes (LCCs) from Chinese quince fruits during the sequential fractionation of pectic and hemicellulosic polysaccharides

Chinese quince (Chaenomeles sinensis) fruits offer a potential source of pectin and hemicellulose. However, the existence of lignin-carbohydrate complexes (LCCs) can negatively impact the extraction of pectin and hemicellulose. In this work, LCCs were sequentially fractionated from Chinese quince during the removal of pectin and hemicellulose. The structures of LCCs were characterized by HPAEC, FT-IR, GPC, Py-GC/MS, TGA and 2D HSQC NMR. The results showed that the carbohydrate content and molecular weight of LCCs was found to be changed significantly after the removal of hemicellulose (KSH). The lignin in Björkman LCCs was found to be linked mainly to galactan and fructan, whereas the lignin LCC-AcOHs was found to be linked mainly to arabinan after the removal of KSH. The isolation of carbonate-soluble pectin (NSP) increased thermal stability of Björkman LCC fraction, however, the isolation of chelator-soluble pectin (CSP) increased the thermal stability of LCC-AcOHs. The S/G ratios of LCC-AcOHs increased and large amounts of S-type lignin released during sequential fractionation of pectin and hemicellulose. These results will be beneficial for understanding the mechanisms of pectin and hemicellulose isolation, thereby facilitating the potential application of Chinese quince as a valuable natural resource for food and other industries.

Protective Effects of Lignin-Carbohydrate Complexes from Wheat Stalk against Bisphenol a Neurotoxicity in Zebrafish via Oxidative Stress.

Lignin-carbohydrate complexes (LCCs) from different lignocellulosic biomass have shown biological qualities as antioxidant and immunostimulant. By contrast, the application of LCCs as protectant against neurotoxicity caused by different compounds is scarce. In this work, two kinds of LCCs with carbohydrate-rich and lignin-rich fractions were obtained from wheat stalk and used to protect against BPA-neurotoxicity in zebrafish. The results showed that BPA at a concentration of 500 µg/L results in neurotoxicity, including significant behavioral inhibition, and prevents the expression of central nervous system proteins in transgenic zebrafish models (Tg (HuC-GFP)). When the zebrafish was treated by LCCs, the reactive oxygen species of zebrafish decreased significantly with the change of antioxidant enzymes and lipid peroxidation, which was due to the LCCs’ ability to suppress the mRNA expression level of key genes related to nerves. This is essential in view of the neurotoxicity of BPA through oxidative stress. In addition, BPA exposure had negative effects on the exercise behavior, the catalase (CAT) and superoxide dismutase (SOD) activity, and the larval development and gene expression of zebrafish larvae, and LCC preparations could recover these negative effects by reducing oxidative stress. In zebrafish treated with BPA, carbohydrate-rich LCCs showed stronger antioxidant activity than lignin-rich LCCs, showing their potential as a neuroprotective agents.

Structural Characterization of Lignin-Carbohydrate Complexes (LCCs) and Their Biotransformation by Intestinal Microbiota In Vitro.

Lignin-carbohydrate complexes (LCCs) have recently emerged as natural products with pharmaceutical and nutraceutical potential. Here, we compared the structure of LCCs from ginkgo (GK, gymnosperms), wheat straw (WST, monocotyledons), and aspen white poplar (AW, dicotyledons). We also investigated the biotransformation of LCCs by intestinal microbiota in vitro. We found that human intestinal microbiota could use LCCs as a carbon source for growth, breaking resistant cross-linkages in LCCs to generate a plethora of short-chain fatty acids (SCFAs) and aromatic compounds with putative beneficial effects on human health. The yield of SCFAs reached 1837.8 ± 44.1 μmol/g using AW LCCs as a carbon source. The biomass of intestinal microbiota increased the fastest using GK LCCs. The greatest amounts of phenolics were present at 4 h in a WST LCCs fermentation system. Many phenolic acids with potential bioactivity were obtained after 24 h fermentation using each LCCs, such as ferulic acid.

Elucidation of the Structure of Lignin-Carbohydrate Complexes in Ginkgo CW-DHP by 13C-2H Dual Isotope Tracer.

To elucidate the chemical linkages between lignin and carbohydrates in ginkgo cell walls, 13C-2H-enriched cell wall-dehydrogenation polymers (CW-DHP) were selectively prepared with cambial tissue from Ginkgo biloba L. by feeding D-glucose-[6-2H2], coniferin-[α-13C], and phenylalanine ammonia-lyase (PAL) inhibitor. The abundant detection of 13C and 2H confirmed that D-glucose-[6-2H2] and coniferin-[α-13C] were involved in the normal metabolism of ginkgo cambial cells that had been effectively labelled with dual isotopes. In the ginkgo CW-DHP, ketal and ether linkages were formed between the C-α of lignin side chains and carbohydrates, as revealed by solid state CP/MAS 13C-NMR differential spectroscopy. Furthermore, the DMSO/TBAH ionic liquids system was used to fractionate the ball-milled CW-DHP into three lignin-carbohydrate complex (LCC) fractions: glucan–lignin complex (GL), glucomannan–lignin complex (GML), and xylan–lignin complex (XL). The XRD determination indicated that the cellulose type I of the GL was converted into cellulose type II during the separation process. The molecular weight was in the order of Ac-GL > Ac-GML > XL. The 13C-NMR and 1H-NMR differential spectroscopy of 13C-2H-enriched GL fraction indicated that lignin was linked with cellulose C-6 by benzyl ether linkages. It was also found that there were benzyl ether linkages between the lignin side chain C-α and glucomannan C-6 in the 13C-2H-enriched GML fraction. The formation of ketal linkages between the C-α of lignin and xylan was confirmed in the 13C-2H-enriched XL fraction.

Efficient production of xylooligosaccharides rich in xylobiose and xylotriose from poplar by hydrothermal pretreatment coupled with post-enzymatic hydrolysis

A promising approach for production of value-added xylooligosaccharides (XOS) from poplar was developed by combining hydrothermal pretreatment and endo-xylanase post-hydrolysis. Results showed that the 35.4% XOS (DP 2–6) and 17.6% low DP xylans (DP > 6) were obtained at the identified optimal condition (170 °C, 50 min) for hydrothermal pretreatment. Structural features of low DP xylans generated during the hydrothermal pretreatment were examined, revealing that low DP xylans are mainly comprised of 4-O-methylglucuronic xylan and are involved in lignin carbohydrate complexes. Moreover, higher pretreatment intensity promoted the cleavage of side-chain substituents including arabinose and glucuronic acid groups. The subsequent endo-xylanase hydrolysis of the pretreatment liquor hydrolyzed low DP xylans, contributing to a significant improvement in xylobiose and xylotriose proportions. This combined strategy resulted in a XOS with conversion yield of 44.6% containing 78.7% xylobiose and xylotriose starting from the initial xylan in raw poplar.

Extraction of Noncondensed Lignin from Poplar Sawdusts with p-Toluenesulfonic Acid and Ethanol.

The traditional pretreatment leads to the recalcitration of C-C bonds during lignin fractionation, thus hindering their depolymerization into aromatic monomers. It is essential to develop an applicable approach to extract noncondensed lignin for its high-value applications. In this work, noncondensed lignins were extracted from poplar sawdust using recyclable p-toluenesulfonic acid for cleaving lignin-carbohydrate complex bonds effectively and ethanol as a stabilization reagent to inhibit lignin condensation. Lignin yield of 83.74% was recovered by 3 mol/L acid in ethanol at 85 °C for 5 h, and carbohydrates were well preserved (retaining 98.97% cellulose and 50.01% hemicelluloses). During lignin fractionation, the acid concentration and extraction time were the major drivers of condensation. Ethanol reacted with lignin at the α-position to prevent the formation of the condensed structure. The extracted lignin depolymerized over the Pd/C catalysts gave a yield of 50.35% of aromatic monomers, suggesting that the novel extraction process provided a promising way for noncondensed lignin production.

Lignin/Carbohydrate Complex Isolated from Posidonia oceanica Sea Balls (Egagropili): Characterization and Antioxidant Reinforcement of Protein-Based Films.

A lignin fraction (LF) was extracted from the sea balls of Posidonia oceanica (egagropili) and extensively dialyzed and characterized by FT-IR and NMR analyses. LF resulted water soluble and exhibited a brownish-to-black color with the highest absorbance in the range of 250–400 nm, attributed to the chromophore functional groups present in the phenylpropane-based polymer. LF high-performance size exclusion chromatography analysis showed a highly represented (98.77%) species of 34.75 kDa molecular weight with a polydispersity index of 1.10 and an intrinsic viscosity of 0.15. Quantitative analysis of carbohydrates indicated that they represented 28.3% of the dry weight of the untreated egagropili fibers and 72.5% of that of LF. In particular, eight different monosaccharides were detected (fucose, arabinose, rhamnose, galactose, glucose, xylose, glucosamine and glucuronic acid), glucuronic acid (46.6%) and rhamnose (29.6%) being the most present monosaccharides in the LF. Almost all the phenol content of LF (113.85 ± 5.87 mg gallic acid eq/g of extract) was water soluble, whereas around 22% of it consisted of flavonoids and only 10% of the flavonoids consisted of anthocyanins. Therefore, LF isolated from egagropili lignocellulosic material could be defined as a water-soluble lignin/carbohydrate complex (LCC) formed by a phenol polymeric chain covalently bound to hemicellulose fragments. LCC exhibited a remarkable antioxidant activity that remained quite stable during 6 months and could be easily incorporated into a protein-based film and released from the latter overtime. These findings suggest egagropili LCC as a suitable candidate as an antioxidant additive for the reinforcement of packaging of foods with high susceptibility to be deteriorated in aerobic conditions.

Direct fractionation of wood chips by deep eutectic solvent facilitated pulping technology and application for enzyme hydrolysis

In the practical application of deep eutectic solvents (DESs) for fractionation of lignocelluloses, the rigorous requirements for the size of starting materials and the long duration of the treatment (even required 12 h) have impeded industrial applications of DES. Herein, the energy-efficient pulping technology was proposed for direct fractionation of wood chips by applying DES (choline chloride: lactic acid) as a cooking solvent. The combination of the pulping technology and DES treatment process enables direct fractionation of wood chips (by bypassing the excessive powderization step) and substantially reduces the pretreatment time owing to the synergistic effect of elevated temperature and pressure. The DES pulping technology can selectively dissolve lignin by cleavage of the lignin-carbohydrate complex (LCC) and β-O-4 linkages, the wood chips can be converted into DES-Pulp at a cooking temperature of 130 °C and preservation time of 1 h, which is an efficient pretreatment method for the enzymatic hydrolysis of wood chips. The enzymatic saccharification ratios of the DES-Pulps are between 35.4% and 88.2% at different DES cooking temperatures. The DES pulping process at a cooking temperature of 140 °C and cooking preservation time of 1 h exhibited the highest cellulose saccharification ratio of 88.2%. For DES-Pulp prepared from low cooking temperature, mechanical treatment can improve their saccharification efficiency, for example, the enzymatic hydrolysis efficiency of the DES-Pulp combined with PFI refining (10 min) was improved from 71.4% to 85.4% at a cooking temperature of 130 °C.

Acid Hydrotropic Fractionation of Lignocelluloses for Sustainable Biorefinery: Advantages, Opportunities, and Research Needs.

This Minireview provides a comprehensive discussion on the potential of using acid hydrotropes for sustainably fractionating lignocelluloses for biorefinery applications. Acid hydrotropes are a class of acids that have hydrotrope properties toward lignin, which helps to solubilize lignin in aqueous systems. With the capability of cleaving ether and ester bonds and even lignin-carbohydrate complex (LCC) linkages, these acid hydrotropes can therefore isolate lignin embedded in the plant biomass cell wall and subsequently solubilize the isolated lignin in aqueous systems. Performances of two acid hydrotropes, that is, an aromatic sulfonic acid [p-toluenesulfonic acid (p-TsOH)] and a dicarboxylic acid [maleic acid (MA)], in terms of delignification and dissolution of hemicelluloses, and reducing lignin condensation, were evaluated and compared. The advantages of lignin esterification by MA for producing cellulosic sugars through enzymatic hydrolysis and lignin-containing cellulose nanofibrils (LCNFs) through mechanical fibrillation from the fractionated water insoluble solids (WIS), and for obtaining less condensed lignin with light color, were demonstrated. The excellent enzymatic digestibility of maleic acid hydrotropic fractionation WISs was also demonstrated by comparing with WISs from other fractionation processes. The recyclability and reusability of acid hydrotropes were also reviewed. Finally, perspectives on future research needs to address key technical issues for commercialization were also provided.

Structural characterization of the lignin-carbohydrate complex in biomass pretreated with Fenton oxidation and hydrothermal treatment and consequences on enzymatic hydrolysis efficiency

In this study, lignin-carbohydrate complexes (LCCs) were isolated from biomass (raw and pretreated) to investigate the structural changes in biomass pretreated by Fenton oxidation and hydrothermal treatment, and their effect on enzymatic hydrolysis. The composition and structure of the LCCs fractions were investigated via carbohydrate analysis, XRD, FT-IR, and 2D HSQC NMR. The biomass degradation rate of yellow poplar and larch during Fenton oxidation and hydrothermal treatment was approximately 30%. Most of the hemicellulose was degraded during pretreatment, while xylan remained in the yellow poplar, and galactan, mannan, and xylan remained in the larch. The fractional yield of glucan-rich LCC (LCC1) in the yellow poplar (raw and pretreated biomass) was high, while that of glucomannan-rich LCC (LCC3) in larch was higher than the yield yellow poplar. Phenyl glycoside, γ-ester, and benzyl ether linkages were observed in the LCCs of yellow poplar, while phenyl glycoside and γ-ester were detected in those of larch. Following pretreatment, the frequencies of β–β′, β-5, and γ-ester in the LCCs of larch were found to be higher than in those of yellow poplar. The efficiencies of enzymatic hydrolysis for the pretreated yellow poplar and larch were 93.53% and 26.23%, respectively. These finding indicated that the β–β′, β-5, and γ-ester linkages included in the pretreated biomass affected the efficiency of enzymatic hydrolysis.

Lytic polysaccharide monooxygenases promote oxidative cleavage of lignin and lignin-carbohydrate complexes during fungal degradation of lignocellulose.

Overcoming lignocellulosic biomass recalcitrance, especially the cleavage of cross-linkages in lignin-carbohydrate complexes (LCCs) and lignin, is essential for both the carbon cycle and industrial biorefinery. Lytic polysaccharide monooxygenases (LPMOs) are copper-containing enzymes that play a key role in fungal polysaccharide oxidative degradation. Nevertheless, comprehensive analysis showed that LPMOs from a white-rot fungus, Pleurotus ostreatus, correlated well with the Fenton reaction and were involved in the degradation of recalcitrant nonpolysaccharide fractions in this research. Thus, LPMOs participated in the extracellular Fenton reaction by enhancing iron reduction in quinone redox cycling. A Fenton reaction system consisting of LPMOs, hydroquinone, and ferric iron can efficiently produce hydroxy radicals and then cleave LCCs or lignin linkages. This finding indicates that LPMOs are underestimated auxiliary enzymes in eliminating biomass recalcitrance.

Conversion of Beech Wood into Antiviral Lignin–Carbohydrate Complexes by Microwave Acidolysis

Conversion of Beech Wood into Antiviral Lignin–Carbohydrate Complexes by Microwave Acidolysis

Enhancement of the antioxidant abilities of lignin and lignin-carbohydrate complex from wheat straw by moderate depolymerization via LiCl/DMSO solvent catalysis

A facile and environmentally-friendly strategy for increasing antioxidant activity is a crucial issue for value-added lignin and lignin-carbohydrate complex (LCC) as alternative antioxidants. However, the antioxidant activities of lignin and LCC by the traditional solid-liquid extraction (SLE) methods were restricted by the relatively lower solubility induced from high molecular weight (Mw), and the less functional groups including, phenolic hydroxyl and carboxyl. To improve the antioxidantion of lignin and LCC, lithium chloride/dimethyl sulfoxide (LiCl/DMSO) solvent fractionation (LDSF) was conducted to increase the functional groups and reduce Mw, in which LiCl/DMSO acted triple roles as solvent, acid, and metal chloride catalyst for the depolymerization reaction synchronously. The β-O-4′ linkages were cleaved to release the phenolic hydroxyl, resulting in decreasing Mw; the hydroxyl of the side-chain of lignin was oxidized into carboxyl. Thus, the lignin (LD-RL) and LCC (LD-LCC) samples from LDSF had a higher syringyl (S)/guaiacyl (G) ratio, phenolic hydroxyl, and carboxyl contents, but less Mw than control groups from SLE. Consequently, they presented more excellent scavenging rates toward DPPH and ABTS radicals, up to 90%. This work provided panoramic perspectives and basics of the green and convenient approach to isolate and modify lignin and LCC for great antioxidantion with LDSF.

APPLICATION OF INTEGRAL QUALITY INDICATORS OF WASTEWATERS FOR INPRODUCTION ECOLOGICAL AND ANALYTICAL CONTROL OF CELLULOSE PRODUCTION

The influence of technological factors (wood species, degree of delignification, the technological regime of pulping) of cellulose semi-products production on composition and qualitative properties of wastewaters of pulp and paper mills following priority of harmonizing of technological and ecological rationing of industrial enterprises. The features of the biopolymer’s composition of the lignin-carbohydrate matrix of coniferous and deciduous species, its functional nature, and self-organization were provided. The main paths of chemical bond destruction in the lignin-carbohydrate complex during delignification and formation of the composition of organic fractions in local wastewaters were shown. The implementation of complementary indicators (COD, BOD5, general and organic carbon, the content of lignin, and volatile phenols) for in-house ecological and analytical control and rationing was substantiated. The dependence of integral indicator COD from the content of fractions of organic components from wastewaters was established. These components are products of destruction and chemical transformation of the lignin-carbohydrate matrix of deciduous and coniferous wood produced during delignification. The composition and the main phenolic components of wastewaters were determined by gas chromatography with mass detection. The correctness of worldwide practice of using "phenolic index" in the system of in-house control of pulp and paper mill was justified.

Mechanism of Deep Eutectic Solvent Delignification: Insights from Molecular Dynamics Simulations

Based on the field of ReaxFF, the pretreatment of a lignin–carbohydrate complex model in a choline chloride-based deep eutectic solvent was proposed. The results showed that the β-O-4 ether and glycosidic bonds in the model were broken at an optimal temperature of 373 K. The best pretreatment solvent was choline chloride/lactic acid (1:2), and 40% of the model compounds were decomposed. Free protons in deep eutectic solvents were one of the critical factors in the process of biomass delignification, and thus acidic hydrogen binding donors generally had a high lignin removal rate, but there was no significant correlation with the acidity of the hydrogen bonding donors. In the deep eutectic solvents of choline chloride/lactic acid, the delignification effect tended to decrease with the increase of lactic acid content. The delignification effect of monocarboxylic acid hydrogen bond donors decreased with the increasing molecular chain length, while the opposite effect of delignification was observed for dicarboxylic acids. The molecular dynamics simulations showed that choline chloride/glycerol (1:2) with a slightly weaker hydrogen bonding network could bind better and solubilize the product molecules, with interaction energies of −170.89 and −61.99 kJ/mol with carbohydrates and phenolic compounds, respectively.

Thermal responses of mountain birch and Siberian larch of an alpine forest-tundra ecotone to climate change

We applied thermogravimetric analysis to ten successive growth rings of Siberian larch and the same number of mountain birch individuals sampled in the alpine forest-tundra ecotone of Kuznetsk Ala Tau mountain ridge to compare physical and chemical responses of the species wood to climate change. Our analysis of the correlation of the wood thermal parameters with air temperature and precipitation revealed that early and latewood cellulose and lignin in the birch were more sensitive to climatic changes as compared to the larch. June–August weather conditions appeared to largely control the chemical composition of the birch early and latewood. Air temperature had a marked influence during synthesis of both early and latewood cell walls, whereas precipitation influenced only latewood. Thermogravimetric analysis of growth rings formed in alpine forest-tundra proved to be an effective tool to study the influence of climatic and weather variability on lignin-carbohydrate complex of deciduous and conifer tree species.

Efficient isolation of organosolv lignin-carbohydrate complexes (LCC) with high antioxidative activity via introducing LiCl/DMSO dissolving

Lignin-carbohydrate complexes (LCC) have shown great potential as biocompatible antioxidants. But it is difficult to isolate LCC efficiently from lignocellulose by traditional Solid-Liquid Extraction method (SLE), which is blamed to the innate bioimpedance caused by the complex supramolecular structure of the lignocellulose, and a great mass transferring resistance between the extracting solution and solid lignocellulose. To release these restrictions above and improve the efficiency of LCC isolation, a modified isolating method named Liquid-Liquid Extraction (LLE) was proposed, in which ball-milled wheat stalk was dissolved in lithium chloride/dimethyl sulfoxide (LiCl/DMSO) solution, then regenerated by dioxane aqueous to extract LL-LCCs. The effect of the LLE on the LCC isolating was evaluated and results showed that both the total yield and antioxidant activity of LL-LCCs were higher than that of control group. It proved the dissolution of wheat stalk in LiCl/DMSO solution could reduce the mass transfer resistance during the extraction. Due to the catalyzation of LiCl as Lewis acid, LL-LCCs had lower molecular weight but more phenolic hydroxyl groups and higher S/G ratios. These factors of LL-LCCs resulted in greater free-radical scavenging ability than control sample. The modified isolation protocol could facilitate the isolation and utilization of LCCs as a free-radical scavenger.

Nonsevere furfural production using ultrasonicated oil palm fronds and aqueous choline chloride-oxalic acid

Furfural is a versatile platform chemical that can be employed to produce green fuel and chemical intermediates. In this study, oil palm fronds were first subjected to ultrasonic pretreatment using an ultrasonic probe in water, which was followed by reaction in an aqueous choline chloride-oxalic acid (16.4 wt% H2O) deep eutectic solvent. The focus of this study was to investigate whether the duration and amplitude of ultrasonic pretreatment improve the furfural yield from oil palm fronds. Mechanoacoustic and sonochemical effects induced by ultrasound waves disrupted the lignin carbohydrate complex in biomass, which increased the hemicellulose availability in the oil palm fronds for furfural production in the subsequent aqueous choline chloride-oxalic acid reaction. By employing ultrasonic pretreatment at 80 % amplitude for 3 min and then an aqueous choline chloride-oxalic acid reaction at 120 °C for 60 min, a furfural yield of 56.5 % was obtained. Characterization studies (e.g., Fourier transform infrared spectroscopy, Brunauer-Emmet-Teller, X-ray diffraction, and field emission scanning electron microscopy) on the oil palm fronds yielded insights into the reaction. Additionally, the reacted oil palm frond residues had a high glucan content, which could be considered a valuable byproduct.