Removal Of Hemicellulose Research Articles

Obtention and Characterization of Microcrystalline Cellulose from Industrial Melon Residues Following a Biorefinery Approach.

Residual melon by-products were explored for the first time as a bioresource of microcrystalline cellulose (MCC) obtention. Two alkaline extraction methods were employed, the traditional (4.5% NaOH, 2 h, 80 °C) and a thermo-alkaline in the autoclave (2% NaOH, 1 h, 100 °C), obtaining a yield of MCC ranging from 4.76 to 9.15% and 2.32 to 3.29%, respectively. The final MCCs were characterized for their chemical groups by Fourier-transform infrared spectroscopy (FTIR), crystallinity with X-ray diffraction, and morphology analyzed by scanning electron microscope (SEM). FTIR spectra showed that the traditional protocol allows for a more effective hemicellulose and lignin removal from the melon residues than the thermo-alkaline process. The degree of crystallinity of MCC ranged from 51.51 to 61.94% and 54.80 to 55.07% for the thermo-alkaline and traditional processes, respectively. The peaks detected in X-ray diffraction patterns indicated the presence of Type I cellulose. SEM analysis revealed microcrystals with rough surfaces and great porosity, which could remark their high-water absorption capacity and drug-carrier capacities. Thus, these findings could respond to the need to valorize industrial melon by-products as raw materials for MCC obtention with potential applications as biodegradable materials.

Obtaining Cellulose Fibers from Almond Shell by Combining Subcritical Water Extraction and Bleaching with Hydrogen Peroxide.

Almond shell (AS) represents about 33% of the almond fruit, being a cellulose-rich by-product. The use of greener methods for separating cellulose would contribute to better exploitation of this biomass. Subcritical water extraction (SWE) at 160 and 180 °C has been used as a previous treatment to purify cellulose of AS, followed by a bleaching step with hydrogen peroxide (8%) at pH 12. For comparison purposes, bleaching with sodium chlorite of the extraction residues was also studied. The highest extraction temperature promoted the removal of hemicellulose and the subsequent delignification during the bleaching step. After bleaching with hydrogen peroxide, the AS particles had a cellulose content of 71 and 78%, with crystallinity index of 50 and 62%, respectively, for those treated at 160 and 180 °C. The use of sodium chlorite as bleaching agent improved the cellulose purification and crystallinity index. Nevertheless, cellulose obtained by both bleaching treatments could be useful for different applications. Therefore, SWE represents a promising green technique to improve the bleaching sensitivity of lignocellulosic residues, such as AS, allowing for a great reduction in chemicals in the cellulose purification processes.

Effect of Surface Treatments on Zea mays Husk and the Behaviour of Husk/Low-Density Polyethylene Composites

(1) Background: The increasing generation of plastic and agricultural wastes is a critical environmental issue that requires urgent attention. Aiming to address this challenge, this study developed a sustainable waste-to-wealth system through the utilization of Zea mays husk as a reinforcing material in the production of green composites. (2) Methods: Delignification, de-hemicellulolysis, and bleaching were employed sequentially to improve the characteristics of the husk. Fourier-transform infrared spectroscopy and scanning electron microscopy confirmed the removal of lignin, hemicellulose, and impurities, and X-ray diffraction analysis determined the degree of crystallinity. Composites were made with treated and untreated husk and recycled low-density polyethylene (LDPE) at various husk-to-LDPE ratios. (3) Results: Mechanical characterization demonstrated that the treated husk composites exhibited superior tensile strength, flexural strength, and hardness compared to the untreated ones and pure LDPE. The treatment did not enhance the thermal stability of the composites, but it did lower their capacity for water absorption and improve their crystallinity. The economic assessment of the husk composite production indicated a total annualized cost of USD 0.9601 per kg, which is significantly lower than the estimated cost for LDPE (USD 1.2 to USD 1.4 per kg). Additionally, it has a much smaller carbon footprint compared to LDPE production. (4) Conclusions: The potential of utilizing treated Z. mays husk as a reinforcing agent in the development of sustainable and cost-effective green composites, improving their overall performance, was established. This approach offers a promising solution for the effective management of plastic and agricultural wastes, contributing to the transition towards a circular economy.

New insights into the influencing mechanisms of hemicellulose removal on dynamic wood-water interactions characterized with low-field NMR

Hemicellulose, one of the most hygroscopic components, highly affected wood properties and wood-water interactions. To get more knowledge about the effects of hemicellulose on wood, this study changed hemicellulose content of wood through hydro-thermal removal of about 8 %, 20 % and 70 %. The dynamic cell water state and distribution during 384 h water absorption and air drying were characterized with low-field nuclear magnetic resonance technique (LFNMR). During water absorption, wood with less hemicellulose initially had higher and faster moisture increase, consisting of more free water in cell lumina and some large voids in cell walls than bound water in cell walls. The highest ratio of free water to bound water reached over 4.5, which was higher than that of untreated wood by over 15 %. This was because hemicellulose removal changed wood-water interaction environments suggested by SEM, FTIR and N2 absorption analysis. Specifically, hemicellulose removal enriched porous structures, especially the mesopore in cell walls. Although sorption sites decreased after hemicellulose removal, increased water paths and water accommodations played a more important role during initial water absorption. Besides, hemicellulose removal facilitated wood air drying, and the decreased moisture included more free water than bound water. This was because the enriched water paths accelerated water exchange, and sorption site decrease after hemicellulose loss reduced wood attraction to water molecules. Therein, the bound water leaving was generally slower than free water for hydrogen bond interaction with wood. The T2 s of bound water and free water were both shortened after hemicellulose removal, possibly because mesopore diameter reduction tightened wood-water bonding. This study provided new insights into understanding role of hemicellulose removal in dynamic wood-water interactions and facilitating development of wood processing technology.

Characteristics of Cellulose Nanofibrils From Arabica Coffee Skin Prepared by the Acid Hydrolysis

Cellulosenanofibrils (CNF) is a new generation material that has high performance, good physics and medical properties and is a renewable material that has been developed from various sources using the acid hydrolysis method. CNF synthesis is generally obtained from logs that have a high amount of cellulose fiber. Cellulose nanofibrils (CNF) from arabica coffee skins have great potential to be developed as raw materials for medicines, which function as wound healing agents, surgical sutures, diet medicines, and skin softeners. CNF is produced from Arabica coffee skin through delignification, namely the removal of lignin and hemicellulose by extraction with alkali until α-cellulose is obtained, then CNF is synthesized through hydrolysis using dilute acid. From the coffee skin extraction results, a high cellulose yield was obtained, reaching above 24.30% and crystallinity reaching 79.60%. Hydrolysis by 10%, 12% and 15% HCl with a reaction time of 2 hours, the respective crystallinity was 80.66; 79.06; and 77.69%.

Isolation of Highly Crystalline Cellulose via Combined Pretreatment/Fractionation and Extraction Procedures within a Biorefinery Concept.

Sustainable production of bio-based materials and chemicals requires integrated approaches which utilize all fractions of lignocellulosic biomass. In this work, highly crystalline cellulose was isolated via combined pretreatment/fractionation and extraction processes from beechwood sawdust. The proposed approach was based on the selective recovery of hemicellulose components in the first step, followed by enhanced delignification in the second step, permitting the efficient recovery of the remaining cellulose via bleaching in the final step. Hydrothermal pretreatment under tailored conditions in neat water or dilute acid resulted in almost complete hemicellulose removal (80-96 wt %) in the liquid fraction. In the second step, the formed surface lignin was isolated via mild extraction while enhanced removal of both native/structural and surface lignin (71 wt %) was achieved by applying the organosolv treatment using dilute sulfuric acid as catalyst. Dilute sulfuric acid pretreatment followed by acid catalyzed organosolv pretreatment proved to be the most efficient combined approach, leading to 80 wt % hemicellulose removal as xylose monomer, and 71 wt % delignification. High crystallinity cellulose (<88%), with an overall cellulose recovery of 68-91 wt % based on native cellulose in parent biomass was isolated in the last step via bleaching of all pretreated biomass solids. The proposed integrated biorefinery procedures that aim to whole "waste" biomass valorization, replacing fossil resources, with the use of green solvents (water, ethanol) at relatively mild temperature/pressure conditions, are in line with the scope of several United Nations Sustainable Development Goals, such as UN SDG 8, 11, 12, and 13.

Upgrading paper-grade bleached hardwood pulp towards dissolving pulp using γ-valerolactone

γ-Valerolactone (GVL) is a promising biomass-based platform compound that can be used for the removal of hemicellulose in pulp. In this study, a paper-grade pulp was treated using GVL to generate dissolving pulp for viscose production. The GVL concentration, treatment temperature, and reaction time had significant effect on the hemicellulose dissolution. The dissolving pulp with α-cellulose content of 92.3% and hemicellulose content of 5.45% was achieved with 60% GVL at 120 °C for 2 h. The Fock reactivity and intrinsic viscosity of the obtained dissolving pulp were 54.6% and 595 mL/g, which is comparable with the commercial product. In addition, GVL spent liquor was also recycled and reused to upgrade paper-grade pulp. By using purified recycled GVL to treat original pulp, the Fock reactivity of pulp was improved, and the cellulose content of as-prepared upgraded pulp increased to 92.1%, which was close to the cellulose content of dissolving pulp obtained from fresh GVL solution, while the intrinsic viscosity decreased significantly to 598 mL/g. Therefore, the efficient reuse of GVL not only ensured the high quality of dissolving pulp, but it also saved production costs and reduced environmental pollution.

Ionic liquid pretreatment of lignocellulose for complete hemicellulose removal to produce high-purity cellulose mixed esters

Strategic valorization of agricultural waste can serve as waste management and promote sustainable biorefineries. Sugarcane bagasse is a readily available lignocellulosic biomass and can be converted into valuable cellulose-based thermoplastics. However, the cellulose purity significantly influences the material properties of the resulting thermoplastics, potentially limiting their applications. Therefore, conventional production necessitates harsh pretreatment of lignocellulose to isolate high-purity cellulose, followed by chemical modification. Here, we demonstrate a facile and green pretreatment method for complete removal of hemicellulose by incubating bagasse in a mixed system of an ionic liquid, 1-ethyl-3-methylimidazolium acetate (EmimOAc), and dimethyl sulfoxide (DMSO) at 140 °C, followed by precipitation in water, achieving >99 % hemicellulose removal. The pretreated bagasse, containing 71 % cellulose and 28 % lignin, underwent homogeneous transesterification with vinyl decanoate and isopropenyl acetate, using EmimOAc as both the solvent and catalyst, assisted by a co-solvent of DMSO. The polysaccharide derivative in the resulting acylated bagasse was separated from the lignin derivative by precipitation in methanol. The obtained polysaccharide derivative with high cellulose purity displayed a high weight-average molar mass of 1.5×106 g mol−1 and a polydispersity of 4. It also exhibited superior thermal stability (thermal degradation temperature, Td−5 %: 359 °C; glass transition temperature, Tg: 144 °C) compared to pulp-derived cellulose acetate decanoate (Td−5 %: 349 °C; Tg: 129 °C).

Fully upgrade bamboo biomass into three multifunctional products through biphasic γ-valerolactone and aqueous phosphoric acid pretreatment

In this manuscript, three components of lignocellulosic biomass were obtained by deconstructing bamboo with γ-valerolactone-H2O biphasic system, and the delignification rate of 80.92 % was achieved at 120 °C for 90 min. Lignin nanospheres with diameters ranging from 75 nm to 2 um could be customized by varying the self-assembly rate. Furthermore, the lignin nanospheres-poly(vinyl alcohol) film was prepared by cross-linking lignin nanospheres and poly(vinyl alcohol), which can obtain 90 % ultraviolet absorption capacity, while the light transmittance in non-ultraviolet band was almost unchanged. At the same time, due to the strong hydrogen formation between lignin nanospheres and poly(vinyl alcohol) bond network, the tensile properties of the composite film were also improved by 30 %. Besides, the high specific surface area of biomass-derived porous biochar (2056 m2/g) can be obtained after carbonization of solid residues at 850 °C for 2 h, which was almost 8 times the specific surface area of the direct biomass carbonization due to the removal of lignin and hemicellulose. biomass-derived porous biochar can be used as an adsorbent, with a CO2 capture capacity of 4.5 mmol g−1 at normal temperature (25 °C, 1 bar). The filtrate after the reaction contained a large amount of hemicellulose oligomers, which can be reacted with dichloromethane at 170 °C for 1 h to obtain the furfural yield of 74 %. In summary, the proposed biorefinery scheme achieves a full-component upgrade of lignocellulose and can be further applied in various downstream fields.

Pretreatment of multiple lignocellulosic batches with recoverable and fermentable deep eutectic solvent (FDES) for co-production of sugar, lignin and lipid

Addressing the high cost of comprehensive utilization of lignocellulose, an efficient and green lignocellulosic biorefinery process was developed in this study, which can achieve the co-production of lignin, sugar and lipid. A series of FDES were prepared using glycerin, choline chloride (ChCl), and H2SO4 for the pretreatment of lignocellulose and ultimately for fermentation. After optimization, the hemicellulose removal reaches 98 %, and enzymatic hydrolysis rate of pretreated solids exceeds 90 %. The FDES was then recovered and reused for pretreatment, in total five batches of lignocellulose were pretreated, only a slight decrease in lignin and hemicellulose removal rate occurred, no significant decrease in lignin yield, and a decrease in solid enzyme hydrolysis from 83.26 % to 78.25 %. Finally, FDES after using five batches was used as a substrate for Rhodotorula glutinis with biomass up to 40.25 g/L and lipid concentration up to 8.33 g/L. In addition, the cellulose was probed with high solid-loading enzymatic hydrolysis, obtaining high concentration of glucose (137.4 g/L) for ethanol fermentation. In conclusion, this study developed a biorefinery technology for the efficient utilization of lignocellulosic fractions and pretreatment solvents, which reduces the cost of DES pretreatments of lignocellulose, and achieves the cogeneration of lignin, sugar and lipids.

A Top-Down Approach to the Fabrication of Flame-Retardant Wood Aerogel with In Situ-Synthesized Borax and Zinc Borate.

In this study, a top-down approach was employed for the fabrication of flame-retardant wood aerogels. The process involved the removal of lignin and the removal of hemicellulose utilizing NaOH concomitantly with the incorporation of ZnO and urea. Subsequently, an in situ reaction with boric acid was conducted to prepare flame-retardant wood aerogels. The morphology, chemical composition, thermal stability, and flame retardancy of the samples were studied. The results show that the NaOH treatment transformed the wood into a layered structure, and flame-retardant particles were uniformly distributed on the surface of the aerogel. The peak heat release rate (PHRR) and total heat release (THR) of the flame-retardant aerogel were significantly reduced compared with the control samples. Meanwhile, its vertical burning test (UL-94) rating reached the V-0 level, and the Limiting Oxygen Index (LOI) could exceed 90%. The flame-retardant wood aerogel exhibited excellent flame retardancy and self-extinguishing properties.

Cellulose nanocrystals isolated from sugarcane bagasse using the formic/peroxyformic acid process: Structural, chemical, and thermal properties

Sugarcane bagasse (SCB) is a renewable biomass source for cellulose extraction. In the pretreatment, SCB is processed to break down the cellulose-lignin-hemicellulose matrix and isolate components. This work proposes a formic/peroxyformic acid process for extracting cellulose nanocrystals (CNCs) from SCB. Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, and solid-state 13C nuclear magnetic resonance (ss- 13C NMR) were employed to evidence the removal of wax, hemicellulose, and lignin from the raw SCB. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and thermogravimetric analysis (TGA) were used for analyzing crystallinity, morphology, and thermal properties. SEM results showed that after lignin removal, the size of purified cellulose fibrils decreased significantly, and the structure of cellulose microfibers became smoother and more apparent. After acid hydrolysis of bleached cellulose microfibers, XRD analysis showed CNCs had the highest crystallinity (70.8 %). In TEM images, rod-like structures of CNCs were measured to be 23 ± 2.7 nm wide and 610 ± 18 nm long. The eco-friendly formic/peroxyformic acid procedure with a chlorine-free bleaching stage produced a white, cellulose-rich solid powder of CNCs.

Preparation of modified wood-based metal nanoparticles synthesized in situ and efficient removal of organic pollutants from wastewater

Wood has excellent properties such as biodegradability, high reactivity and rich channel skeleton structure. However, the defects such as hole blockage and limited specific surface area limit the application of wood-based materials in wastewater treatment. Therefore, in this research, wood substrates (DTWS) were treated using a deep eutectic solvent method, which was able to remove both lignin and hemicellulose from wood. Wood-based carriers with high specific surface area and high chemical activity were formed. The DTWS-Ag material was formed by growing Ag nanoparticles (NPs) in wood channels by hydrothermal method. The results showed that with the increase of lignin and hemicellulose removal, the degradation performance of DTWS-Ag material showed a volcanic trend due to the interaction between Ag and the inner wall of the pipe. The pore size and the amount of Ag NPs are very important to the degradation rate of dye molecules. DTWS-4-Ag composite material makes wood pore diameter and Ag NPs production reach a high balance, so that it has the highest degree of reduction. DTWS-4-Ag showed high catalytic degradation efficiency and stability for methylene blue degradation, with the degradation efficiency up to 98.3 %. This low-cost, renewable wood-based filter has high dye degradation efficiency and can be widely used in practical wastewater treatment.

One-pot extraction of nanocellulose from raw durian husk fiber using carboxylic acid-based deep eutectic solvent with in situ ultrasound assistance

Nanocellulose (CNF) has emerged as a promising alternative to synthetic petroleum-based polymers, but the conventional preparation process involves multiple tedious steps, heavily dependent on chemical input, and proves cost-inefficient. This study presented an, in situ ultrasound-assisted extraction using deep eutectic solvent (DES) based on choline chloride and oxalic acid for more facile production of CNF from raw durian husk fibers. FESEM analysis confirmed the successful extraction of web-like nanofibril structure with width size ranging from 18 to 26 nm. Chemical composition analysis and FTIR revealed the selective removal of lignin and hemicellulose from the raw fiber. As compared to post-ultrasound treatment, in situ ultrasound-assisted extraction consistently outperforms, yielding a higher CNF yield with finer fiber width and significantly reduced lignin content. Integrating this eco-friendly in situ ultrasonication-assisted one-pot extraction method with a 7.5 min interval yielded the highest CNF yield of 58.22 % with minimal lignin content. The superior delignification ability achieved through the proposed in situ ultrasound-assisted protocol surpasses the individual efficacy of DES and ultrasonication processes, neither of which yielded CNF in our experimental setup. This single-step fabrication process significantly reduces chemical usage and streamlines the production steps yielding web-structured CNF that is ideal for sustainable application in membrane and separator.

Efficacy and Functional Mechanisms of a Two-Stage Pretreatment Approach Based on Alkali and Ionic Liquid for Bioconversion of Waste Medium-Density Fiberboard.

A novel pretreatment strategy utilizing a combination of NaOH and 1-Butyl-3-methylimidazolium chloride ([Bmim]Cl) was proposed to enhance the enzymatic hydrolysis of abandoned Medium-density fiberboard (MDF). The synergistic effect of NaOH and [Bmim]Cl pretreatment significantly improved the glucose yield, reaching 445.8 mg/g within 72 h, which was 5.04 times higher than that of the untreated samples. The working mechanism was elucidated according to chemical composition, as well as FTIR, 13C NMR, XRD, and SEM analyses. The combined effects of NaOH and [Bmim]Cl led to lignin degradation, hemicellulose removal, the destruction and erosion of crystalline regions, pores, and an irregular microscopic morphology. In addition, by comparing the enzymatic hydrolysis sugar yield and elemental nitrogen content of untreated MDF samples, eucalyptus, and hot mill fibers (HMF), it was demonstrated that the presence of adhesives and additives in waste MDF significantly influences its hydrolysis process. The sugar yield of untreated MDF samples (88.5 mg/g) was compared with those subjected to hydrothermal pretreatment (183.2 mg/g), Ionic liquid (IL) pretreatment (406.1 mg/g), and microwave-assisted ionic liquid pretreatment (MWI) (281.3 mg/g). A long water bath pretreatment can reduce the effect of adhesives and additives on the enzymatic hydrolysis of waste MDF. The sugar yield produced by the combined pretreatment proposed in this study and the removal ability of adhesives and additives highlight the great potential of our pretreatment technology in the recycling of waste fiberboard.

Higher efficiency of vanadate iron in heterogeneous Fenton-like systems to pretreat sugarcane bagasse and its enzymatic saccharification.

Pretreatment is crucial for effective enzymatic saccharification of lignocellulose such as sugarcane bagasse (SCB). In the present study, SCB was pretreated with five kinds of heterogeneous Fenton-like systems (HFSs), respectively, in which α-FeOOH, α-Fe2O3, Fe3O4, and FeS2 worked as four traditional heterogeneous Fenton-like catalysts (HFCs), while FeVO4 worked as a novel HFC. The enzymatic reducing sugar conversion rate was then compared among SCB after different heterogeneous Fenton-like pretreatments (HFPs), and the optimal HFS and pretreatment conditions were determined. The mechanism underlying the difference in saccharification efficiency was elucidated by analyzing the composition and morphology of SCB. Moreover, the ion dissolution characteristics, variation of pH and Eh values, H2O2 and hydroxyl radical (·OH) concentration of FeVO4 and α-Fe2O3 HFSs were compared. The results revealed that the sugar conversion rate of SCB pretreated with FeVO4 HFS reached up to 58.25%, which was obviously higher than that under other HFPs. In addition, the surface morphology and composition of the pretreated SCB with FeVO4 HFS were more conducive to enzymatic saccharification. Compared with α-Fe2O3, FeVO4 could utilize H2O2 more efficiently, since the dissolved Fe3+ and V5+ can both react with H2O2 to produce more ·OH, resulting in a higher hemicellulose and lignin removal rate and a higher enzymatic sugar conversion rate. It can be concluded that FeVO4 HFP is a promising approach for lignocellulose pretreatment.

Sustainable wheat straw pretreatment process by self-produced and cyclical crude lactic acid

The purpose of this study was to investigate an environmentally friendly and recyclable pretreatment approach that would enhance the enzymatic digestibility of wheat straw. Wheat straw was pretreated using self-produced crude lactic acid obtained from enzymatic hydrolysate fermentation by Bacillus coagulans. Experimentally, crude lactic acid at low concentration could achieve a pretreatment effect comparable to that of commercial lactic acid. After pretreatment at 180 °C for 60 min with 2.0 % crude lactic acid, hemicellulose could be effectively separated and high recovery of cellulose was ensured, achieving cellulose recovery rate of 95.5 % and hemicellulose removal rate of 92.7 %. Excellent enzymatic hydrolysis was accomplished with a glucose yield of 99.7 %. Moreover, the crude lactic acid demonstrated acceptable pretreatment and enzymatic hydrolysis performance even after three repeated cycles. This not only effectively utilizes the pretreatment solution, but also offers insights into biomass pretreatment using other fermentable acids.

Fabrication and property characterization of biocomposite based on polyamide 11 and AP1 green ramie fiber modified with epoxy

AbstractIn this article, Vietnam ramie fiber from Moc Chau, Son La province was chosen as a reinforcement for polyamide 11 (PA11) to prepare full–biocomposites. To enhance the compatibility and adhesion with the matrix, the original ramie fiber (oRF) was treated with Ca(OH)2 solution (tRF) and then modified by epoxy (mRF). Properties and structure of these fibers were characterized by tensile test, chemical composition, Fourier transform infrared spectroscopy (FT‐IR), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM). The obtained results showed the removal of hemicellulose and lignin after treatment improved the morphology and mechanical properties of the fiber. Rheology in melting state indicated the increase in the torque of PA11 matrix by adding tRF and mRF. The improvement in mechanical properties was observed for both PA11/tRF and PA11/mRF composites. After modification, epoxy on the fiber surface enhanced the adhesion and compatibility with the matrix. This led to a strong increase in Young's modulus, tensile strength and flexural strength of about 37%, 57%, and 33%, respectively. tRF and mRF also improved thermal stability of the composite as shown in TGA and DSC analysis. Finally, mRF showed a better compatibility with PA11 than tRF by observation of SEM images.

Selective Removal of Hemicellulose by Diluted Sulfuric Acid Assisted by Aluminum Sulfate.

Hemicellulose can be selectively removed by acid pretreatment. In this study, selective removal of hemicellulose was achieved using dilute sulfuric acid assisted by aluminum sulfate pretreatment. The optimal pretreatment conditions were 160 °C, 1.5 wt% aluminum sulfate, 0.7 wt% dilute sulfuric acid, and 40 min. A component analysis showed that the removal rate of hemicellulose and lignin reached 98.05% and 9.01%, respectively, which indicated that hemicellulose was removed with high selectivity by dilute sulfuric acid assisted by aluminum sulfate pretreatment. Structural characterizations (SEM, FTIR, BET, TGA, and XRD) showed that pretreatment changed the roughness, crystallinity, pore size, and functional groups of corn straw, which was beneficial to improve the efficiency of enzymatic hydrolysis. This study provides a new approach for the high-selectivity separation of hemicellulose, thereby offering novel insights for its subsequent high-value utilization.

Extraction and characterization of nanocellulose from waste of date palm "Phoenix dactylifera″ as reinforcement of polymer composites.

The cellulose is the most abundant and renewable polymer in nature. It is characterized by its biodegradability that can help to establish a friendly environment. The main objective of this study is intended to characterize the nanocellulose obtained from waste date palm, including the dried palms (DP) and the fresh palms (FP) by implementing chemical methods (hydrolysis with H2SO4). Physical properties, morphology, the elemental composition and the thermal stability were determined by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), zeta sizer, scanning electron microscopy (SEM), whereas energy dispersive X-ray (EDX) and thermogravimetric analysis (TGA), respectively. FTIR, SEM and EDX results, revealed the effective removal of impurities, hemicellulose and lignin. Palm sample residues contained 35.99% of cellulose and 33.12% of cellulose nanocrystals (CNC) for DP, and 36.17% of cellulose and 34.35% of CNC for FP. The CNCs have higher crystallinity than the raw fibers and Zeta sizer was between 25 and 1150 nm. TGA analysis showedthat DP exhibited greater thermal resistance.