Structure Of Hemicellulose Research Articles

Quantitative analysis of intermolecular forces in cellulose microfibrils and hemicellulose with AFM nano-colloidal probes

It is an interesting research topic to study the interfacial interactions between hemicellulose and cellulose, specifically how hemicellulose's structure affects its binding to cellulose nanofibers. Our research proposes that dispersion interaction play an important role in this interfacial interaction, more so than electrostatic forces when considering the adherence of cellulose to xylan. To quantify these interactions, the Atomic Force Microscope (AFM) colloidal probe technique is applied to measure the intermolecular forces between cellulose nanofibers, which are attached to the probe and xylan. These measured forces are then analyzed in relation to the length, diameter and functional groups of the nanocellulose, as well as the molecular weight and side chains of the xylan. Moreover, the predominance of dispersion forces by contrasting the adhesive forces before and after the grafting of a large nonpolar group onto xylan. This modification significantly reduces contact between the cellulose and xylan backbone, thereby markedly diminishing the dispersion interactions. Parallel to the AFM experiments, molecular dynamics (MD) simulations corroborate the experimental results and support our hypotheses. Collectively, these findings contribute to a deeper understanding of polysaccharide interactions within lignocellulose.

Synthesis and Characterization of Porous Materials from Waste Wheat Bran

The purpose of this study was to investigate how the amount of ZnCl2 and temperature affect the process of converting waste wheat bran, known for its hemicellulose struc-ture, into porous material. The characterization of the wheat bran was done using proximate and primary component analysis, and Thermogravimetric analysis (TG) test, Fourier Transform Infrared Spectroscopy (FT-IR) spectra, Energy-dispersive X-ray spectroscopy (EDS) results, and Scanning electron microscopy (SEM) images. The influence of temperature on the surface areas of activated carbons is more significant than the impact of varying the amount of ZnCl2. When the carbonization temperature reached 500 °C, porous structures developed, and the highest surface areas achieved for all impregnation ratios (1:1, 2:1, and 3:1) were 1234, 1478, and 1422 m2/g, respectively. Activated carbon was found to have acidic (0.88 mmol/g) and basic (0.54 mmol/g) functional groups on its surface, after being synthesized through carbonization at 500 °C using ZnCl2 at a 2:1 impregnation ratio in accordance with Boehm titration. This promising activared carbon made from wheat bran, activated by ZnCl2, is efficient and environmentally friendly, and it is a potential solution for water pollution treatment.

Characterization of Syzygium cumini (L.) Skeels (Jamun Seed) Particulate Fillers for Their Potential Use in Polymer Composites.

Syzgium cumini (L.) Skeels powder (S. cumini powder), also known as Jamun, is well-known for its various medical and health benefits. It is especially recognized for its antidiabetic and antioxidant properties. Thus, S. cumini powder is used in various industries, such as the food and cosmetic industries. In this work, the fruit of S. cumini was utilized; its seeds were extracted, dried, and ground into powder. The ground powders were subjected to various techniques such as physicochemical tests, Fourier transform infrared (FTIR) spectroscopy, X-ray diffractometry (XRD), particle size analysis, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and antioxidant analysis. From the physicochemical tests, it was revealed that the jamun seed filler contained cellulose (43.28%), hemicellulose (19.88%), lignin (23.28%), pectin (12.58%), and wax (0.98%). The FTIR analysis supported these results. For instance, a peak at 2889 cm-1 was observed and associated with CH stretching, typically found in methyl and methylene groups, characteristic of cellulose and hemicellulose structures. The XRD results demonstrated that the crystallinity index of the jamun seed filler was 42.63%. The particle analysis indicated that the mean (average) particle size was 25.34 μm. This observation was ensured with SEM results. The EDX spectrum results showed the elemental composition of the fillers. Regarding thermal degradation, the jamun seed filler had the ability to withstand temperatures of up to 316.5 °C. Furthermore, endothermic and exothermic peaks were observed at 305 °C and 400 °C, respectively. Furthermore, the antioxidant property of the powder displayed a peak scavenging activity of 91.4%. This comprehensive study not only underscores the viability of S. cumini powder as a sustainable and effective particulate filler in polymer composites but also demonstrates its potential to enhance the mechanical properties of composites, thereby offering significant implications for the development of eco-friendly materials in various industrial applications.

Nutrient Removal Efficiencies in a Bioretention Cell Using Pre-Treated Coconut By-Product as Carbon Source

Abstract In this research, the appropriateness of alkali pre-treatment on coconut by-products was managed by exposing coconut husk and shell to 2M NaOH. The powdered samples were analysed for morphology observation, Fourier Transform Infrared (FTIR), Particle Size Analyzer (PSA), and water quality tests. Weakening the hemicellulose structure resulted from subjecting the coconut shell to alkali pre-treatment shown in the morphology observation. Furthermore, the FTIR analysis exhibited the presence of O-H stretch in all pre-treated samples representing an indication for occurring the lignin breakdown, while an absence of the C=O functional group was shown in both additive samples after their subjection to alkali pre-treatment. In PSA analysis, the particles of all samples were found finer than the particle size distribution standards, in which the smallest D50 was obtained for the treated coconut shell (TCS), followed by untreated coconut shell (UCS), untreated coconut husk (UCH), and treated coconut husk (TCH). Among all the powdered samples (TCS, UCS, UCH, and TCH) analysed in this study, only TCH values met the ranges provided and recommended by the Urban Stormwater Management Manual for Malaysia (MSMA) and the Australian Department of Sustainability, Environment, Water, Population, and Communities (DSEWPC). Meanwhile, a poor removal rate for total suspended solids (TSS) was attained due to the contribution of TSS by the filter media which caused the TSS rates to surpass the inlet values. Additionally, the presence of a high concentration of total phosphorous (TP) in all the tested samples indicated their capabilities to provide PO43 in the bioretention cell, which is a vital nutrient for the plant’s growth. In contrast, Ammoniacal Nitrogen (AN) with a concentration rate as low as 4 mg/L was observed throughout the test periods which showed a significant reduction compared to the rate of AN at the inlet samples ranged between 5.2 and 11.4 mg/L. The findings indicated that coconut by-products, when subjected to an alkali pre-treatment process, are appropriate for incorporation as additives in bioretention filter media.

Enhancing biogas production through photocatalytic pretreatment of rice straw co-digested with cow dung and food waste using a novel g-C3N4/SiO2/bentonite catalyst

This study investigates the application of a novel composite photocatalyst, g-C3N4/SiO2/ Bentonite, for rice straw pretreatment, aiming to enhance biogas production in anaerobic digestion. The photocatalytic pretreatment disrupts rice straw's lignin and hemicellulose structures, reducing silica content for improved microbial degradation. Five 2 L anaerobic digesters were employed with rice straw as the substrate and co-digestion materials, including cow dung and food waste. Rice straw treated with the g-C3N4/7.5% SiO2/5% Bentonite catalyst exhibited a remarkable 37% increase in methane yield compared to untreated rice straw. This photocatalytic process led to a 31% increase in cellulose content and a 30% reduction in lignin after 6 hours of pretreatment. Simultaneously, silica content in the rice straw decreased to 6.4% after 6 hours, resulting in a 48% increase in the carbon proportion. These findings underscore the potential of integrated photocatalysts for significantly enhancing biogas production efficiency through the pretreatment of lignocellulosic biomass.

Delignification of wood fibers using a eutectic carvacrol–methanesulfonic acid mixture analyses of the structure and fractional distribution of lignin, cellulose, and hemicellulose

AbstractDelignification and fractional pretreatments are essential for valorization of wood biomass in various bioproducts. Herein, lignocellulose wood fibers were exposed to a eutectic mixture (EM) of carvacrol and methanesulfonic acid for different times. The resulting structural and chemical alterations in biomass were explored in terms of the fiber morphology and fractional chemical composition through fiber image analysis, field-emission scanning electron microscopy, high-performance liquid chromatography, and a novel approach based on fluorescence-lifetime imaging microscopy (FLIM). The autofluorescence of the lignocellulose fibers, which was primarily due to lignin with contributions from cellulose and hemicellulose, enabled application of FLIM in lignocellulose compositional analysis in micro-scale. FLIM analysis revealed that EM treatment efficiently removed lignin from the outer fiber layers. Furthermore, the effective EM treatment time was 3 h (with a residual lignin content of ~ 7 wt%), after which defects were observed on the fibers and the cellulose chains started breaking. This degradation was also indicated by a shift of the lifetime spectra toward the fluorescence lifetime of cellulose with increasing treatment time. Overall, our findings provide valuable insights to the response of lignocellulose fibers to EM treatment, contributing to the important goal of wood biomass application in bioproducts.

Expression and Characterization of a Thermostable α-Glucuronidase from Geobacillus kaustophilus

Fossil fuels are a crucial resource for the global economy, but they also contribute to greenhouse gas emissions and environmental pollution. Lignocellulosic biomass, which includes cellulose, hemicellulose, and lignin obtained from plants, is a promising alternative to fossil fuels. It can help address these problems while reducing environmental impact. Enzymatic pre-treatment is used to degrade lignocellulosic biomass into subunits. The degradation of the hemicellulose structure involves accessory enzymes of industrial importance, such as α-glucuronidase. α-glucuronidases (EC 3.2.1.139) catalyze the hydrolysis of the α-1,2-glycosidic bond between α-D-glucuronic acid (GlcA) or its 4-o-methyl ether form (MeGlcA) and d-xylose units in the structure of xylooligosaccharides. The aim of this study was cloning, heterologous expression and biochemical characterization of the α-glucuronidase enzyme from the thermophilic bacterium Geobacillus kaustophilus. With this aim, the codon optimized α-glucuronidase gene was cloned into pQE-30 vector, overexpressed in E. coli BL21 (DE3), and purified with nickel affinity chromatography. The biochemical characterization of the purified α-glucuronidase revealed that the enzyme has activity at elevated temperatures between 65-90 °C. Additionally, Geobacillus kaustophilus α-glucuronidase enzyme showed higher activity at acidic pH values from pH 4.0 to 6.5. This is the first study to report the gene cloning, recombinant expression and biochemical characterization of α-glucuronidase which could be used as accessory enzyme from a thermophilic bacterium Geobacillus kaustophilus.

Banana Peel (Musa ABB cv. Nam Wa Mali-Ong) as a Source of Value-Adding Components and the Functional Properties of Its Bioactive Ingredients.

Banana peel (BP) is the primary by-product generated during banana processing which causes numerous environmental issues. This study examines the physical attributes, proximate analysis, glycoarray profiling, antioxidant abilities, and prebiotic activity of BP. The analysis demonstrated that carbohydrates constituted the primary components of BP and the glycoarray profiling indicated that BP contains multiple pectin and hemicellulose structures. BP also contained phenolic compounds, including (+)-catechin and gallic acid, flavonoid compounds, and antioxidant activities. BP demonstrated prebiotic effects by promoting the proliferation of advantageous gut bacteria while inhibiting the growth of harmful bacteria. The prebiotic index scores demonstrated that BP exhibited a greater capacity to promote the growth of beneficial bacteria in comparison to regular sugar. The study demonstrated the potential of the BP as a valuable source of dietary fibre, bioactive compounds, and prebiotics. These components have beneficial characteristics and can be utilised in the production of food, feed additives, and functional food.

Ab Initio and Kinetic Modeling of β-d-Xylopyranose under Fast Pyrolysis Conditions.

Lignocellulosic biomass is an abundant renewable resource that can be upgraded to chemical and fuel products through a range of thermal conversion processes. Fast pyrolysis is a promising technology that uses high temperatures and fast heating rates to convert lignocellulose into bio-oils in high yields in the absence of oxygen. Hemicellulose is one of the three major components of lignocellulosic biomass and is a highly branched heteropolymer structure made of pentose, hexose sugars, and sugar acids. In this study, β-d-xylopyranose is proposed as a model structural motif for the essential chemical structure of hemicellulose. The gas-phase pyrolytic reactivity of β-d-xylopyranose is thoroughly investigated using computational strategies rooted in quantum chemistry. In particular, its thermal degradation potential energy surfaces are computed employing Minnesota global hybrid functional M06-2X in conjunction with the 6-311++G(d,p) Pople basis set. Electronic energies are further refined by performing DLPNO-CCSD(T)-F12 single-point calculations on top of M06-2X geometries using the cc-pVTZ-F12 basis set. Conformational analysis for minima and transition states is performed with state-of-the-art semiempirical quantum chemical methods coupled with metadynamics simulations. Key thermodynamic quantities (free energies, barrier heights, enthalpies of formation, and heat capacities) are computed. Rate coefficients for the initial steps of thermal decomposition are computed by means of reaction rate theory. For the first time, a detailed elementary reaction kinetic model for β-d-xylopyranose is developed by utilizing the thermodynamic and kinetic information acquired from the aforementioned calculations. This model specifically targets the initial stages of β-d-xylopyranose pyrolysis in the high-pressure limit, aiming to gain a deeper understanding of its reaction kinetics. This approach establishes a systematic strategy for exploring reactive pathways, evaluating competing parallel reactions, and selectively accepting or discarding pathways based on the analysis. The findings suggest that acyclic d-xylose plays a significant role as an intermediary in the production of key pyrolytic compounds during the pyrolysis of xylose. These compounds include furfural, anhydro-d-xylopyranose, glycolaldehyde, and dihydrofuran-3(2H)-one.

Hemicellulose-rich paper-grade pulp as raw material for regenerated fibres in an ionic liquid-based process

Hemicellulose-rich pulp raw materials are avoided in the production of man-made cellulosic textile fibres due to hemicellulose reactivity with the currently used industrial solvent systems. Incorporation of hemicelluloses in regenerated fibres could, however, increase the share of used wood biomass and thus improve the environmental footprint of regenerated fibre products. Superbase ionic liquids have shown potential in dissolving and regenerating all the major wood polymers i.e. cellulose, hemicellulose and lignin into regenerated products. In this work, regenerated fibres were spun from hemicellulose-rich softwood and eucalyptus paper-grade pulps and eucalyptus dissolving pulp using a superbase ionic liquid [mTBNH][OAc]. Before dissolution and spinning, intrinsic viscosities of the paper-grade pulps were adjusted either enzymatically or by using a mild acid-treatment to improve dope rheology for dry-jet wet spinning. In fibre spinning, hemicellulose was found to regenerate in high yield and the obtained regenerated fibres had high dry tenacities (5.3 to 15 cN/dtex). The best mechanical properties were measured from fibres with high hemicellulose content (17.3% (w/w)). Pulp pretreatment was found to be critical for achieving good mechanical properties. Acid-pretreatment, which modified both cellulose and hemicellulose, yielded regenerated fibres with better mechanical properties compared to an enzyme-pretreatment which did not alter the hemicellulose structure. Removal of hemicellulose substituents and hydrolysis of hemicellulose backbone in acid-pretreatment may be the key to improved mechanical properties in hemicellulose-containing regenerated fibres. Enzymatic peeling and imaging with a xylan-specific monoclonal antibody (CCRC-M138) suggest that hemicelluloses were enriched to the outermost layers of the regenerated fibres.

Physio-chemical and Thermal Characterization of Demineralized Poultry Litter using Mechanical Sizing Fractioning, Acid Solvents, and Deionized Water

Poultry litter is an organic waste composed of manure, feathers, and bedding, containing both organic and inorganic elements. Inorganic elements corrode and agglomerate the reactors when poultry litter is thermally converted to biochar, bio-oil or combusted. Demineralizing poultry litter through mechanical size fractioning, acid solvent, and deionized water can decrease the inorganic elements' composition. This study investigates to identify the effects of different demineralization methods on the physio-chemical and thermal characteristics of poultry litter. Statistical analysis (p-value of 0.001) showed that the pretreatment methods reduced the inorganic elements. Mechanically fractioned poultry litter with particle sizes of 1.19-2.36mm and 2.37-5.00mm showed a low inorganic element composition of 7.85% and 9.19% when demineralized. The acid solvent and PL:DI treatments varied their extraction effectiveness depending on the type of inorganic element removed, ranging from 9.65-11.73% of the total inorganic element composition. PL:AcOH treatment had the lowest ash content at 6.89% from 12.33%. Mechanical size fractioned samples had the lowest moisture content, ranging from 2.53% to 4.65%. All the samples had high fixed carbon content except for PL:<1.18mm sample. Volatile matter for PL: AcOH, PL: DI, and PL:2.37-5.00mm samples were higher than the UT: PL and other treated samples. The treated samples noted a low C, high O, S, N, H/C, and O/C and comparable H content with UT: PL sample. Removal of inorganic elements increased the sample's high heating value, with the PL:2.37-5.00mm sample having the highest at 17.60 MJ Kg-1. The FTIR spectra of the demineralized sample revealed a reduction in the transmittance band, indicating the decomposition of the cellulose and hemicellulose structures. TGA-DTG supported the findings by noting a shift in temperature increase with peak temperatures higher than UT: PL sample samples. The degradation occurred at temperatures up to 380°C, noting the degradation of the cellulose and hemicellulose structure of the demineralized poultry litter.

Structural changes of hemicellulose during pulping process and its interaction with nanocellulose

It is believed that hemicellulose plays a crucial role in binding cellulose and lignin in plant cells. It may provide significant implications through figuring out the interaction between hemicellulose and microfibers and gaining insights how the structure of hemicellulose affects its association with cellulose nanofibers. Herein, the hemicellulose and nanocellulose fractions from pulps obtained by controlling the H-factors of kraft pulping process were quantitatively evaluated for their adsorption behavior using QCM-D. The results showed that harsher cooking (corresponding to high H-factor) significantly affected the chemical composition of hemicellulose, leading to a decrease of its molecular weight and gradually turning it into a linear structure. Hemicellulose possesses a strong natural affinity for CNC-coated sensors. The hemicellulose from the pulp cooked by high H-factor process decreases its ability to adsorb onto nanocellulose, the adsorption rate also slows down, and the conformation of the adsorbed layer changes which makes the binding weak and reversible. In conclusion, the pulping process in high H-factor significantly changed the structure of hemicellulose, leading to a variation in the strength of its interaction with nanocellulose.

CHANGES IN HEMICELLULOSE STRUCTURE ASSOCIATED WITH THE TRANSITION FROM EARLYWOOD TO LATEWOOD AT JUVENILE WOOD IN CRYPTOMERIA JAPONICA

The chemical composition and variations in chemical structure of hemicellulose in earlywood (EW) and latewood (LW) of two individual Japanese cedar trees (C-Boka and T-Boka) were investigated. The trees were cultivated under different growth conditions: C-Boka grew slowly in a forest, while T-Boka grew rapidly in a location rich in nutrients and sunshine. For the chemical structure of hemicellulose, arabinoglucuronoxylan (AGX) showed varied side-chain substitution rates with glucuronic acid and different molecular weights in the transition between EW and LW. In contrast, the fundamental composition of glucomannan/galactoglucomannan (GM/GGM) was relatively unchanged between EW and LW. The modification of AGX and GM/GGM from EW to LW differed between C-Boka and T-Boka and might be influenced by the growth rate of the trees.

Label free electrochemical sensors for Pb(II) detection based on hemicellulose extracted from Opuntia Ficus Indica cactus

We aim to develop an electrochemical sensor for a divalent metal ion (lead II), a highly toxic water contaminant. We explore a sensor formed with a hemicellulose polysaccharide extracted from the Opuntia Ficus Indica cactus associated with agarose as a sensitive layer deposited on a gold electrode. This sensor combines the functional groups of hemicellulose that could form a complex with metal ions and agarose with gelling properties to form a stable membrane. The sensor demonstrated a loading ability of Pb2+, with higher affinity compared to other metal ions such as Hg2+, Ni2+, and Cu2+, thanks to the chemical structure of hemicellulose. The detection was measured by square wave voltammetry based on a well-defined redox peak of the metal ions. The sensor shows high sensitivity towards Pb2+ with a detection limit of 1.3 fM. The application in river and sea water using the standard addition method for lead detection was studied.

Chemical pretreatment of corncob for the selective dissolution of hemicellulose and lignin: influence of pretreatment on the chemical, morphological and thermal features

The aim of this work was to remove the hemicellulose and lignin fraction from corncob using chemical pretreatments, and to stablish the effect of that on the composition, microstructure, and thermal properties of corncob. The biomass was pretreated with H2SO4 and NaOH solution to dissolve hemicellulose and lignin portion. Likewise, the biomass pretreated was characterized by scanning electron microscope, IR spectroscopy and TGA methods. It was found that the acid pretreatment disrupt the hemicellulose structure by hydrolysis of glycoside bonds. Moreover, the corncob morphology becomes flaky after acid pretreatment due to dissolution of hemicellulose. The lignin is removed during alkaline pretreatment by solvation of aryl groups. In addition, the crystalline morphology of cellulose fibers was disrupted, increasing the surface area. The pretreatment of corncob with 1.0% H2SO4 and 0.1 M NaOH solubilized ∼42.6% and ∼20.9% of the biomass, respectively. The soluble products were analyzed by FTIR, Fehling test, and calorimetric analysis, to stablish their composition and heat content. The hydrolysis of hemicellulose leads to the release of the monomeric sugars and soluble oligomers. Moreover, the lignin of corncob releases more energy per unit of mass, making it an energy-denser component of corncob.

Structural characterization of corn fiber hemicelluloses extracted by organic solvent and screening of degradation enzymes

An integrated treatment coupling peracetic acid delignification, dimethyl sulfoxide extraction, and ethanol precipitation were performed to isolate hemicellulose from de-starched corn fiber. Based on chemical composition, molecular weight distribution, methylation, and nuclear magnetic resonance spectroscopy, it is proposed that hemicelluloses in corn fiber were composed of two polysaccharides, glucuronoarabinoxylan (about 80 %) and xyloglucan (about 20 %). Xylose (about 46 %) and arabinose (about 32 %) were the main components in glucuronoarabinoxylan. More than half of the xylose units in the glucuronoarabinoxylan backbone chain were substituted at O-2 and/or O-3 by various monomers or oligomeric side chains. Based on structure analysis, five hemicellulases were selected and added to Penicillium oxalicum MCAX enzymes for enzymatic hydrolysis of corn fiber. The results showed that the addition of hemicellulases increased the sugar yield of corn fiber. These results demonstrate the effectiveness of enzyme consortium constructed by elucidating the chemical structure of hemicellulose in corn fiber for the degradation of corn fiber and also provide a general solution for the rational construction of targeted and efficient enzyme systems for the degradation of lignocellulosic biomass.

The volatile organic compounds emission mechanism of pretreated bamboo during heat treatment

Heat treatment can be used to improve bamboo product quality. Pretreatment of the bamboo material can reduce the energy consumption of heat treatment. However, large quantities of volatile organic compounds (VOCs) are released during the bamboo heat treatment process, causing potential problems for the environment and human health. In this study, the effects of pretreatment with sodium hydroxide and zinc chloride solutions on VOCs emissions during heat treatment were investigated. We also explored chemical and structural changes of heat-treated bamboo. The VOCs released by untreated bamboo during heat treatment were mainly aldehydes, alcohols, alkanes, and esters. Alcohol and alkane contents decreased as treatment temperature increased, accompanying the emergence of more complex chemicals. Compared with untreated bamboo, sodium hydroxide pretreatment destroyed the hemicellulose structure, released stable VOCs under heat treatment, and did not produce acidic compounds; ether compounds increased significantly with increase in temperature. The catalysis of zinc chloride pretreatment degraded hemicellulose during heat treatment. The relative contents of aldehydes and esters released from zinc chloride pretreated bamboo during heat treatment increased significantly with temperature. Up to 69.76 % of aldehyde compounds were released at 160 °C, among which the relative proportion of furfural reached 37.23 %. These results may provide theoretical support for controlling VOCs emissions from different pretreated bamboo materials during heat treatment, which is also conducive to the subsequent recycling of VOCs.

Upgrading catalytic efficiency of activated carbons by tailoring lignocellulosic biomass waste for sustainable conversion of glycerol to solketal

This study introduces a novel strategy for boosting both surface acidic properties and textural features of a series of activated carbons from petiole of Mauritia flexuosa Linnaeus fillius, a lignocellulosic biomass waste. The structure, state and concentration of lignin, cellulose and hemicellulose into the selected precursor underwent a reconfiguration protocol aiming at tunning surface features of the carbons-based catalyst chemically activated with H3PO4. In fact, the modified precursors gave rise to activated carbons that boast surface area of up to 2349 m2.g−1 and total acidity ranging from 2.22 to 3.13 mmol.g−1, making them suitable candidate to promote the conversion of glycerol to solketal. The catalysts were successfully applied in the solvent-free acetalization of glycerol with acetone achieving glycerol conversion higher than 83% (selectivity around 98% toward solketal) with remarkable turnover frequencies as well as a notable reusability in consecutive runs. Further, it was noticed that the diversity of acid strength of the reactive sites played an important role in each step of the reaction mechanism synergically improving catalytic performance. The physicochemical and surface chemistry properties of the activated carbons were characterized by means of N2 adsorption/desorption isotherms, thermal analysis, elemental analysis, surface functional groups titration, X-rays diffraction, scanning electron microscopy and FTIR spectroscopy.

Populus endo-glucanase 16 localizes to the cell walls of developing tissues.

The hemicelluloses comprise a group of matrix glycans that interact with cellulose microfibrils in plant cell walls and play important roles in establishing wall architecture. The structures of hemicelluloses are determined by carbohydrate-active enzymes (CAZymes) that synthesize, integrate, and break down these polymers. Specifically, endo-glucanase 16 (EG16) enzymes, which are related to the well-known xyloglucan endotransglycosylase/hydrolase (XTH) gene products in Glycoside Hydrolase Family 16 (GH16), have been implicated in the degradation of the β(1,4)-linked backbone of mixed-linkage β(1,3);β(1,4)-glucans (MLG) and xyloglucans. EG16 members are single-copy genes found in most plant clades but are absent from many eudicots, including the model plant Arabidopsis thaliana. Until recently, EG16 members had only been characterized in vitro, establishing their substrate specificity, protein structure, and phylogenetic history, but their biological function was unknown. Here we used a hybrid polar, Populus alba× Populus grandidentata (P39), as a model to examine EG16 expression, subcellular localization, and pheno- and chemotypes of EG16-downregulated P39 plants. Populus EG16 expression is strong in young tissues, but RNAi-mediated downregulation did not impact plant growth nor the fine structure of the hemicellulose xyloglucan, suggesting a restricted or currently unknown role in angiosperm physiology.

Influence of chemically-modified cotton straw fibers on the properties of asphalt mortar

Cotton straw fibers have an important influence on the performance of asphalt mixtures. However, the modification of cotton straw fibers and the performance characterization between the treated cotton straw fibers and asphalt are still lack of understanding. To obtain a better performance improvement technical scheme of cotton straw fibrous asphalt mortar. In this study, sodium hydroxide, silane coupling agent (KH550), and glacial acetic acid (CH3COOH) were used to modify the surface of cotton straw fibers. The modification mechanism and basic properties of the cotton straw fibers were investigated. The effect of the modified fibers on the performance of asphalt mortar was studied using cone penetration, softening point, ductility, and dynamic shear rheology tests. The results showed that the CH3COOH- and KH550-modified fibers produce new acetyl C-O and Si-O deformation vibration absorption peaks, respectively. The three modification methods destroy the hemicellulose structure in the cotton straw fibers. The post-modification surface impurities, roughness, and basic properties of the fibers are reduced, increased, and improved, respectively. An increasing cotton straw fiber dosage continuously improves the high temperature performance of asphalt mortar, but reduces ductility. A fiber dosage of 2 % yields optimized the high temperature performance and the ductility. Under this dosage, the CH3COOH-modified cotton straw fibrous asphalt mortar exhibits a better comprehensive performance. Its shear strength and softening point, as compared to the matrix asphalt increase by 3.21 times and 14.99 %, respectively, and the ductility reduces by 23.94 %, all the measured properties meet the technical specifications of road petroleum asphalt. The results provide more bases for the application of cotton straw fibers in road engineering.