Cellulose Molecules Research Articles

Ultralight Cellulose-Derived Carbon Nanofibers from Freeze-Drying Emulsion Towards Superior Microwave Absorption

Carbon nanofibers (CNFs) are usually prepared by the carbonization of cellulose aerogels obtained from freeze-drying. However, cellulose with low concentration (below 1 wt%) is required to maintain the good porosity of the aerogels due to the strong hydrogen bonding between the cellulose molecules. In order to address this problem, here, ultralight cellulose-derived CNFs have been fabricated by freeze-drying cyclohexane (CHE)/cellulose nanofiber emulsions and carbonization. Field emission scanning electron microscopy, Raman spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and Fourier transform infrared spectroscopy are used to characterize the resulting CNFs. It is found that the CNFs consist of three-dimensional carbon networks, whose microstructure is easily adjusted by changing the CHE ratio (from 0 to 25 vol%) in the emulsions. The CNFs with high porosity are attributed to the fact that CHE as the oil phase can effectively weaken the hydrogen bonding and reduce the aggregation of the cellulose nanofibers. Carbon lattice defects and residual oxygen-containing functional groups are regarded as polarization centers, leading to the enhancement of dielectric loss. The conductive carbon networks also improve the conductive loss. All these factors improve the microwave absorption performance of the CNFs. So, the produced CNFs exhibit a superior electromagnetic wave performance with a minimum reflection loss of −42.18 dB and effective absorption bandwidth up to 4.9 GHz at 2 mm with a filling ratio of 2 wt%. This work provides a simple, low-cost, and sustainable synthesis route for CNFs used for ultralight high-performance microwave absorption materials.

Effect of the coconut fibers and cement on the physico-mechanical and thermal properties of adobe blocks

This work aimed to investigate the effect of cement and coconut fibers on the thermal and physico-mechanical characteristics of adobe blocks. Thus, a clayey raw material consisting of kaolinite (62 wt%), quartz (31 wt%), goethite (2 wt%) with a plasticity index of 21.5 % was used to manufacture adobe blocks amended with cement and coconut fibers. First the adobe blocks were formulated with an optimal cement content of 4 wt% before adding coconut fibers up to 1 wt%. The physico-mechanical and thermal characteristics of manufactured composites were then studied. According to the results obtained, the incorporation of coconut fibers into the clay-cement matrix decreases the apparent density and volume shrinkage and increases the porosity of the adobe blocks. The presence of coconut fibers in adobe blocks promotes the phenomenon of water absorption. The combined effect of the formation of calcium silicate hydrate (CSH) and hydrogen bonds between fibers molecules and those of clayey minerals leads to an improvement in the mechanical properties of adobe blocks. The thermal conductivity of adobe blocks decreases with the fiber content due to the presence of pores and cellulose molecules in the fibers which have an insulating nature. Taking into account their physico-mechanical and thermal properties, adobe blocks containing 0.6 wt% coconut fibers and 4 wt% cement are suitable for building sustainable habitats and thermally comfortable.

Attapulgite-Reinforced Cellulose Hydrogels with High Conductivity and Antifreezing Property for Flexible Sensors.

Ionic conductive cellulose hydrogels are some of the most promising candidates for flexible sensors. However, it is difficult to simultaneously prepare cellulose hydrogels with high mechanical strength, good ionic conductivity, and antifreeze performance. In this work, a natural clay (attapulgite)-reinforced cellulose hydrogel was fabricated. Through a one-pot method, cellulose and attapulgite were dispersed in a concentrated ZnCl2 solution. The obtained hydrogel exhibited a dual network of hydrogen bonds and Zn2+-induced ionic interactions. Attapulgite serves as an inorganic filler that can regulate the hydrogen-bonding density among cellulose molecules and provides abundant channels for fast ion transport. By optimizing the attapulgite loading, a mechanically strong (compressive strength up to 1.10 MPa), tough (fracture energy up to 0.36 MJ m-3), highly ionic conductive (4.15 S m-1), and freezing-tolerant hydrogel was prepared. These hydrogels can be used for sensitive and stable human motion sensing, demonstrating their great potential for healthcare applications.

Identification of a Fomitopsis pinicola from Xiaoxing’an Mountains and Optimization of Cellulase Activity

Brown-rot fungi are large fungi that can decompose the cell walls of wood; they are notable for their secretion of diverse and complex enzymes that synergistically hydrolyze natural wood cellulose molecules. Fomitopsis pinicola (F. pinicola) is a brown-rot fungus of interest for its ability to break down the cellulose in wood efficiently. In this study, through a combination of rDNA-ITS analysis and morphological observation, the wood decay pathogen infecting Korean pine (Pinus koraiensis Siebold and Zucc.) was identified. Endoglucanase (CMCase) and β-glucosidase were quantified using the DNS (3,5-Dinitrosalicylic acid) method, and the cellulase activity was optimized using a single-factor method and orthogonal test. The results revealed that the wood-decaying fungus NE1 identified was Fomitopsis pinicola with the ITS accession number OQ880566.1. The highest cellulase activity of the strain reached 116.94 U/mL under the condition of an initial pH of 6.0, lactose 15 g·L−1, KH2PO4 0.5 g·L−1, NH4NO3 15 g·L−1, MgSO4 0.5 g·L−1, VB1 0.4 g·L−1, inoculated two 5 mm fungal cakes in 80 mL medium volume cultured 28 °C for 5 days. This laid a foundation for improving the degradation rate of cellulose and biotransformation research, as well as exploring the degradation of cellulose by brown rot fungi.

Removal of Arsenic from Contaminated Water by Polypyrrole-Based Adsorbents

Worldwide, there is growing concern over the toxicity of arsenic in drinking water. The US Environmental Protection Agency and Central Pollution Control Board (India) have set a safe limit of 50 parts per billion for arsenic in drinking water. Millions of people are at immediate risk due to high concentrations of arsenic in drinking water, particularly in developing nations where arsenic poisoning symptoms have been observed. One of the essential techniques described in this article is the absorption of arsenic from contaminated water by sustainable cellulosic materials like jute and wood sawdust after suitable modification. Jute and sawdust are cheap and abundantly available in South Asia. They are functionalized with polypyrrole coating by in situ chemical polymerization of pyrrole in aqueous medium in the presence of ferric chloride. Polypyrrole-coated jute fabric (with 11.28% polypyrrole add-on) and polypyrrole-coated sawdust (with 5.28% polypyrrole add-on) are found to be excellent adsorbers of arsenic ion (As3+) from water. The effect of dosage of polypyrrole-coated adsorbents, treatment time and pyrrole concentration on the As removal efficiency have been investigated in this work. The arsenic concentration in water is determined using a microwave plasma atomic emission spectrometer with the highest level of accuracy. Maximum As removal efficiency by the polypyrrole-coated sawdust and polypyrrole-coated jute fabric is found to be 80.90% and 97.3%, respectively, from a 50 mL, 7.5 parts per million As solution with a dosage of 1 g at neutral pH. The polypyrrole-coated jute and sawdust are characterized by Fourier-transform infrared spectroscopy to understand the chemical interaction between cellulose and polypyrrole molecules. The scanning electron microscope studies reveal a uniform coating of polypyrrole around the surface of jute fibre and sawdust particles. Thermo-gravimetric analysis shows good thermal stability of jute and sawdust after polypyrrole coating.

Utilization of papermaking black liquor as liquid phase for hydrothermal carbonization of corn stalks: The unique role of alkali for production of hydrochar

Papermaking black liquor (BL) contains a large amount of organic matter, alkali, and salt, which has high value in industrial and agricultural production. In the present paper, hydrothermal carbonization (HTC) technology has been employed to deal with BL and corn stalk (CS) under various conditions. A variety of analytical technologies, including Fourier Transform Infrared Spectrometer, X-Ray Diffraction, element analyzer, comprehensive thermal analyzer, scanning electron microscope, chromatography/mass spectrometry, TOC analyzer, and density functional theory (DFT), were used to characterize the physicochemical properties of hydrochar and aqueous phase product. The effects of experimental parameters (temperature, solid-liquid ratio, and time) on the HTC of BL and CS were systematically investigated. The higher energy yield and densification of hydrochar prepared by our HTC technology were obtained at 260 ℃ in 30 min with a solid-liquid ratio of 1:3. Mechanism study indicates that NaOH, which comes from the original BL, could effectively facilitate the cleavage of β–O–4 bond in lignin and β–1–4 glycosidic bond in cellulose and hemicellulose molecules. Hemicellulose and cellulose are more susceptible to degradation relevant to the lignin in the presence of NaOH. Elementary analysis shows that the dosage of BL is important for improving energy densification of hydrochar. The combustion characteristics show that hydrochar presents a thermochemical behavior, which is close to bituminous coal. Owing to hydroxyl ion in NaOH ion pair was consumed in the series of dehydrogenation reactions, pH of HTC aqueous phase product significantly decreases from 11 to 13 in original BL to 4.8–5. Such results indicate that a completely change for the components of BL could be obtained by our HTC technology, which provide a novel idea for the treatment of Papermaking BL without concentration.

Saccharification of Different Delignified Sawdust Masses from Various Trees Along the Lagos Lagoon in Nigeria

Sawdust, a major waste product of the forestry industry, is accumulating along the Lagos Lagoon in Lagos, Nigeria, without it being effectively managed. Besides its use in The saccharification of sawdust could contribute to the development of renewable energy sources and feedstock for bioproduct development. The process is, however, not that straightforward as variables such as the type of cellulase enzyme, pretreatment of the cellulose substrate, and optimizing of cellulase to cellulose ratio are a few that need to be optimized for the process to be effective in terms of glucose production.manufacturing sound-absorbing boards to reinforce concrete beams and for energy purposes, its potential as a renewable energy source and feedstock for bio-product development has not yet been realized. Cellulose, a glucose biopolymer and structural component of cellulose can be hydrolyzed by a hydrolytic enzyme known as cellulase. During the process, the enzyme breaks the B-1,4-glucosidic bond, which keeps the glucose units together, and by acting on this bond, numerous glucose units are released. As part of sawdust, the cellulose molecule is not freely available for the degradation action of the cellulase enzyme as it is strongly associated with lignin, which acts as bio-glue, keeping cellulose and hemicellulose together. Delignification is an effective technique that was used to make the sawdust from ten different trees along the Lagos Lagoon in Nigeria more susceptible to saccharification by cellulase isolated from the fungus Aspergillus niger. Delignified and non-delignified sawdust masses between 2 mg and 10 mg were incubated with the A. niger cellulase solution (2 mg.mL-1), whereafter, the amount of sugar produced by the cellulase action was determined. The percentage saccharification of each sawdust material was also linked with the amount of sugar produced during cellulase action. From these investigations was concluded that delignification increased sugar production when almost all the masses of different sawdust materials were degraded. It was also observed that the ratio of sawdust mass to enzyme concentration is an important variable that influences the effectiveness of the saccharification process. The percentage saccharification of the various sawdust materials was also determined, and it indicated that the highest percentage of saccharification was not obtained when the highest amount of sawdust was degraded, producing the highest amount of sugar.

Acid Mine Drainage Precipitates from Mining Effluents as Adsorbents of Organic Pollutants for Water Treatment.

Acid mine drainage (AMD) is one of the main environmental problems associated with mining activity, whether the mine is operational or abandoned. In this work, several precipitates from this mine drainage generated by the oxidation of sulfide minerals, when exposed to weathering, were used as adsorbents. Such AMD precipitates from abandoned Portuguese mines (AGO, AGO-1, CF, and V9) were compared with two raw materials from Morocco (ClayMA and pyrophyllite) in terms of their efficiency in wastewater treatment. Different analytical techniques, such as XRD diffraction (XRD), Fourier Transform Infrared spectroscopy (FTIR), N2 adsorption isotherms, and Scanning Electron Microscopy (SEM) with Energy Dispersive X-ray (EDX) were used to characterize these natural materials. The adsorption properties were studied by optimizing different experimental factors, such as type of adsorbent, adsorbent mass, and dye concentration by the Box-Behnken Design model, using methylene blue (MB) and crystal violet (CV) compounds as organic pollutants. The obtained kinetic data were examined using the pseudo-first and pseudo-second order equations, and the equilibrium adsorption data were studied using the Freundlich and Langmuir models. The adsorption behavior of the different adsorbents was perfectly fitted by the pseudo-second order kinetic model and the Langmuir isotherm. The most efficient adsorbent for both dyes was AGO-1 due to the presence of the cellulose molecules, with qm equal to 40.5 and 16.0 mg/g for CV and MB, respectively. This study confirms the possibility of employing AMD precipitates to adsorb organic pollutants in water, providing valuable information for developing future affordable solutions to reduce the wastes associated with mining activity.

A regenerated cellulose fiber with high mechanical properties for temperature-adaptive thermal management

The escalating global population has led to a surge in waste textiles, posing a significant challenge in landfill management worldwide. In this work, ionic liquid 1-butyl-3-methylimidazole acetate ([Bmim]OAc) and DMF (N, n-dimethylformamide) were used as solvents to dissolve waste denim fabric, then vanadium dioxide (VO2) nanoparticles were introduced into the spinning solution, and cellulose fibers were regenerated by dry-wet spinning process, to promote the recycling of waste cotton fabric. Finally, regenerated cellulose fibers with high added value were prepared by dry-wet spinning. Through this innovative strategy, on the one hand, because VO2 can form a large number of hydrogen bonds between the regenerated cellulose molecules, and realize the cross-networking structure of the molecular chains inside the fiber, the mechanical properties of the regenerated cellulose fibers are enhanced. On the other hand, due to the thermal phase transformation characteristics of VO2, it also endows the regenerated cellulose fiber unique intelligent temperature control function. Compared with the pristine regenerated fiber, the tensile stress of the regenerated fiber after adding VO2 nanoparticles (F-VO2) increased by 25.6 %, reaching 158.68 MPa. In addition, the F-VO2 fibric provides excellent intelligent temperature control, reducing temperatures by up to 6.7 °C.

Superfast, large-scale harvesting of cellulose molecules via ethanol pre-swelling engineering of natural fibers

Cellulose molecules, as the basic unit of biomass cellulose, have demonstrated advancements in versatile engineering and modification of cellulose toward sustainable and promising materials in our low-carbon society. However, harvesting high-quality cellulose molecules from natural cellulosic fibers (CF) remains challenging due to strong hydrogen bonds and unique crystalline structure, which limit solvents (such as ionic liquid, IL) transport and diffusion within CF, making the process energy/time-intensively. Herein, we superfast and sustainably engineer biomass fibers into high-performance cellulose molecules via ethanol pre-swelling of CF followed by IL treatment in the microwave (MW) system. Ethanol-pre-swelled cellulosic fibers (SCF) feature modified morphological and structural distinctions, with improved fiber width, pore size, and specific surface area. The ethanol in the SCF structure is appropriately removed through MW heating and cooling, leaving transport and diffusion pathways of IL within the SCF. Such strategy enables the superfast (140 s) and large-scale (kilogram level) harvesting of cellulose molecules with high molecular weight, resulting in high-performance, versatile cellulose ionogel with a 300 % increase in strength and 1027 % in toughness, monitoring human movement, external pressure, and temperature. Our strategy paves the way for time/energy-effectively, sustainably harvesting high-quality polymer molecules from natural sources beyond cellulose toward versatile and advanced materials.

Ethanol Vapor‐Induced Synthesis of Robust, High‐Efficiency Zinc Ion Gel Electrolytes for Flexible Zn‐Ion Batteries

The evolution of flexible Zn‐ion batteries (FZIBs) significantly hinges on the development of gel electrolytes, characterized by their mechanical properties, ionic conductivity, and environmentally friendly production processes. The prevailing challenge in this domain has been devising a gel electrolyte that encapsulates all these critical attributes effectively for practical application. This study presents a novel zinc ion gel (Zn‐gel) electrolyte developed for FZIBs, synthesized via ethanol vapor‐induced assembly of cellulose molecules. This innovative process fosters significant hydrogen bonding and ion‐complexation with Zn2+ ions, resulting in a gel with exceptional mechanical strength (0.88 MPa), high ion transference (over 0.7), and impressive ionic conductivity (8.39 mS cm−1). The Zn‐gel enables a FZIB to achieve a reversible capacity of 207.3 mAh g−1 and over 93% Coulombic efficiency after 500 cycles, devoid of liquid electrolyte. Highlighting a promising route for high‐performance, eco‐friendly gel electrolytes, this research advances flexible electronics and portable device applications, demonstrating the profound potential of bio‐based polymers in enhancing energy storage technology.

TEMPO/CaBr2/Ca(OCl)2 oxidation of hardwood bleached kraft pulp in water at pH 10 with aqueous Ca(OH)2 solution

The conventional TEMPO/NaBr/NaOCl system for oxidation of cellulose to prepare nanocellulose materials has some shortcomings in terms of controlling side reactions and clogging in washing/filtration process. A new TEMPO/CaBr2/Ca(OCl)2 system was then developed to oxidize a hardwood bleached kraft pulp (HBKP) in water at pH 10 (TEMPO = 2,2,6,6-tetramethylpiperidine-1-oxyl radical). An aqueous Ca(OH)2 solution was used to continuously control the reaction mixture at pH 10. After oxidation, the reaction mixture containing the oxidized products and chemicals was directly filtered on a 40-μm-mesh nylon filter and the water-insoluble oxidized products on the filter were washed with water without any clogging. The carboxy content increased to 1.5 mmol/g and the mass recovery ratio decreased to 87.7% as the amount of Ca(OCl)2 was increased to 10.0 mmol/g-HBKP. The oxidized products contained calcium ions but almost no chloride ions, indicating that they comprised almost pure –(COO)2Ca groups. The ready filtration and washing of the oxidized products was probably owing to the low degree of dissociation of the –(COO)2Ca groups in water. The X-ray powder diffraction (XRD) and solid-state carbon 13 nuclear magnetic resonance (13C-NMR) analyses revealed that the crystallinities and crystal widths of the original cellulose I structure were mostly retained in the oxidized products. However, size-exclusion chromatography and viscosity analyses revealed that substantial depolymerization occurred on the cellulose and oxidized cellulose molecules in the products, as in TEMPO/NaBr/NaOCl-oxidized products.Graphical

A strategy for introducing biomass naringin molecules into regenerated cellulose fibers: Construction of both low fibrillation tendency and high strength lyocell fibers

Lyocell fiber is regarded as one of the most representative green fibers, which has higher strength than other regenerated cellulose fibers, but is easily fibrillated when produced. Here, we developed a strategy to strengthen lyocell fiber by the strong interaction between the small molecules of biomass and polymeric cellulose chain networks. The green biomass naringin molecules containing phenolic hydroxyl structures are introduced into the solvent (N-methyl morpholine-N-oxide, NMMO) system of producing lyocell fiber, and the rational arrangement of naringin and cellulose molecular chains is precisely controlled through fiber-forming process of dry-jet-wet spinning and wet-drafting. Due to the interaction of strong hydrogen bond between naringin and cellulose molecules, the strength, toughness and Young’s modulus of the obtained composite fibers reached 500.78 ± 33.57 MPa, 28.16 ± 4.65 MJ/m3 and 23.06 ± 1.01 GPa, respectively, which were 86.96 %, 44.86 % and 48.97 % higher than those of pure lyocell fibers. In addition, naringin molecules have two directional (the longitudinal and transverse direction) bonding effects, which not only improves the mechanical performance of the fiber, but also reduces the fibrillation. The simultaneously improvement of mechanical performance and the reduction of fibrillation tendency are unprecedented in related studies, which contributes to the production of better performance lyocell fibers.

Ion‐Conducting Molecular‐Grafted Sustainable Cellulose Quasi‐Solid Composite Electrolyte for High Stability Solid‐State Lithium‐Metal Batteries

AbstractCellulose‐based solid electrolyte possesses the characteristics of low cost, high strength, and sustainability, and has great potential in the field of solid‐state lithium metal batteries. However, the large hydrogen bonds between cellulose molecules make the molecular chains tightly arranged, and hinder the ion conduction, seriously limiting its further development. Herein, an ion‐conducting molecular grafting strategy is proposed for the fabrication of cellulose acetate quasi‐solid composite electrolyte (CLA‐CN‐LATP QCE) with a superior ionic conductivity of 1.25 × 10−3 S cm−1 at room temperature. Benefited from grafted functional molecules, the assembled symmetrical battery exhibits low polarization voltage and highly stable lithium stripping/plating cycling of more than 1200 h at 0.1 mA cm−2 current density. Moreover, it endows LFP|CLA‐CN‐LATP QCE|Li battery with excellent long‐cycle stability of 1500 cycles at 0.5 C and 25 °C and superior capacity retention of 92.1%. Importantly, this work provides an effective strategy for further opening the ion transport channel between cellulose molecular chains and improving the interface properties of electrolytes and electrodes.

A fresh perspective on dissociation mechanism of cellulose in DMAc/LiCl system based on Li bond theory

In this case, various characterization technologies have been employed to probe dissociation mechanism of cellulose in N,N-dimethylacetamide/lithium chloride (DMAc/LiCl) system. These results indicate that coordination of DMAc ligands to the Li+–Cl− ion pair results in the formation of a series of Lix(DMAc)yClz (x = 1, 2; y = 1, 2, 3, 4; z = 1, 2) complexes. Analysis of interaction between DMAc ligand and Li center indicate that Li bond plays a major role for the formation of these Lix(DMAc)yClz complexes. And the saturation and directionality of Li bond in these Lix(DMAc)yClz complexes are found to be a tetrahedral structure. The hydrogen bonds between two cellulose chains could be broken at the nonreduced end of cellulose molecule via combined effects of basicity of Cl− ion and steric hindrance of [Li (DMAc)4]+ unit. The unique feature of Li bond in Lix(DMAc)yClz complexes is a key factor in determination of the dissociation mechanism.

A perspective on cellulose dissolution with deep eutectic solvents

Currently, membrane manufacturing relies heavily on fossil-based solvents and polymers, resulting in significant negative impacts on human health and the environment. Thus, there is an urgent need for eco-friendly, low-toxicity, and sustainable solvents and polymers to comply with the United Nations’ sustainable development goals. Cellulose, as a green, natural, and abundant polymer, offers a sustainable source for membrane manufacturing. However, a significant challenge exists in dissolving cellulose due to strong intermolecular and intramolecular hydrogen bonds within cellulose molecules. Deep eutectic solvents (DESs), which contain both hydrogen bond donor and acceptor groups, have received significant attention as alternative solvents for cellulose dissolution owing to their low cost, low toxicity, environmentally friendly nature, ease of synthesis, and versatility. This review examines experimental studies, and theoretical approaches, highlighting key findings and factors influencing cellulose dissolution in deep eutectic solvents.

Succession of bacterial and fungal communities during the mud solarization of salt-making processing in a 1000-year-old marine solar saltern

A 1000-year-old marine solar saltern in Hainan Island, South China, is in the continuation of traditional skills involving mud soak and solarization for three days to accumulate salt, which is a unique process contributing to the selection of highly halophilic microbes related to salt quality and flavor. Herein, the successions of physicochemical properties and bacterial and fungal communities of muds from the saltern were investigated during the processing of mud solarization. The results showed that Na+, Cl−, Mg2+ and total nitrogen were the main factors in explaining the fluctuation of the fungal community, whereas the bacterial community was predominantly determined by Ca2+, total kalium and total phosphorus. During three days of mud solarization, the soil bacterial alpha diversity in the saltern was significantly lower than that of the surroundings, whereas the fungal alpha diversity showed an opposite trend. The bacterial functional groups with the same survival and adaptation strategies remained relatively stable, while the dominant functional type in fungi changed from monotropic to complex trophic mode. Additionally, some unidentified fungi species were increasingly found in mud. The abundances of Saitozyma, Solicoccozyma and Wallemia (Basidiomycota) increased and may contribute to the salt flavor through decomposing cellulose molecules into glucose due to their higher β-glucosidase activity, while the harmful fungal genera including Inocybe and Paraconiothyrium decreased obviously due to the stresses of salinity and solar exposure. These results showed that the traditional salt-making skills associated with mud solarization have selected a high abundance of beneficial halophilic microbes to increase the salt quality and flavor. Our findings not only reveal the underlying mechanisms for the long-history salt-making skills of this 1000-year-old unusual cultural heritage but also are highly valuable for bioprospecting to develop novel halophilic bacteria and fungi for modern chemistry industries.

Structural analyses of supernatant fractions in TEMPO-oxidized pulp/water reaction mixtures separated by centrifugation and dialysis

Side reactions occurring on cellulose during 2,2,6,6-tetramethylpiperidine-1-oxyl radical (TMEPO)-catalyzed oxidation have not been considered to be significant. Then, TEMPO-oxidized hardwood and softwood bleached kraft pulps (HBKP and SBKP) were prepared with an excess NaOCl·5H2O. Supernatant fractions (SFs) were obtained in the aqueous reaction mixtures of TEMPO-oxidized pulps by centrifugation and dialysis. The SFs with carboxyl contents of 5.0 and 4.2 mmol/g were obtained in the yields of 19 % and 30 % from HBKP and SBKP, respectively. These carboxy contents are much higher than those (2.6–2.7 mmol/g) of the precipitate fractions in the TEMPO-oxidized pulps. Solid-state 13C NMR spectra and other analyses revealed that the water-soluble β-(1 → 4)-polyglucuronic acids were predominantly present in the SFs. In addition, water-insoluble TEMPO-oxidized cellulose nanocrystals were present in the SFs, but they constituted less than ~10 % of the SFs. The mass-average degrees of polymerization (DPw) of the SFs obtained from HBKP and SBKP were 166 and 155, respectively, whereas the original HBKP and SBKP had DPw values of 1990 and 2140, respectively. These substantial depolymerization and formation of the water-soluble β-(1 → 4)-polyglucuronic acids occur on cellulose and oxidized cellulose molecules as side reactions during TEMPO-catalyzed oxidation, which should be considered for structural analyses of TEMPO-oxidized products.

Development of Plumeria alba extract supplemented biodegradable films containing chitosan and cellulose derived from bagasse and corn cob waste for antimicrobial food packaging

With the increase in global plastic pollution due to conventional plastic packaging (petroleum-derived), bioplastics have emerged as an alternative green source for practising a circular economy. This research aimed to extract cellulose from bagasse and corn cob waste and utilized in mixed form to prepare bioplastic film. The mixed cellulose was further reinforced with natural substances such as chitosan, bentonite, and P. alba extract. These newly developed bioplastics films were characterized by various physical tests like film thickness, moisture content, water solubility and spectroscopic techniques such as Fourier transform infrared (FTIR), scanning electron microscopy-energy dispersive spectroscopic (SEM-EDX), thermal gravimetric analysis (TGA), and ultraviolet-visible (UV–Vis) spectroscopy for opacity testing. The results revealed the enhanced bioplastic thermal and mechanical characteristics through robust interactions between cellulose and bentonite molecules. Moreover, incorporating chitosan solution as reinforcements in bio-composite films resulted in improved water barrier properties. The results indicated lower absorption in the UV range of 250–400 nm, attributed to the absence of UV-absorbing groups. Finally, their biodegradability was tested in soil, and 85.3 % weight loss of bioplastic films was observed after 50 days of the experiment which is the main task of this research. The antimicrobial properties of bioplastic films have been evaluated, and showed an inhibition zone of 16 mm against E. coli. After 12 days of incubation of sherbet berries, complete spoilage is identified in the control group compared to those covered with the bioplastic film. This outcome is attributed to the antioxidant and antimicrobial activities provided by chitosan and P. alba extract in the bioplastic film. The comprehensive outcomes of this study suggest the potential future adoption of these entirely bio-derived, environmentally sustainable and biodegradable bioplastic films as a viable substitute for the plastic packaging currently present in the market.

Green environmental protection and sustainable utilization of straw: Investigation for molecular dynamics of highland barley straw fiber to enhancing road performance of asphalt

This study explores the impact of highland barley straw (HBS) fiber, an environmentally friendly material, on the molecular dynamics and performance of asphalt. Despite the widespread use of fibers in enhancing asphalt performance, molecular-scale investigations are lacking. In this study, molecular dynamics software was employed to model matrix asphalt and three types of HBS fiber-modified asphalt with varying cellulose contents (8.62 wt%, 15.88 wt%, 22.06 wt%). Thermodynamic parameters mean squared displacements (MSD), radial distribution function (RDF), free volume fraction (FFV), and mechanical parameters were analyzed through simulation to understand the diffusion behavior of HBS cellulose molecules in asphalt and study the modification mechanism. The findings revealed that the 8.62 wt% cellulose-modified asphalt had the slowest diffusion rate, with the most favorable temperature for asphalt diffusion being 298.15 K. Integration of HBS cellulose molecules facilitated the self-aggregation process of asphaltene-asphaltene and improved the compatibility between asphaltene-resin, resulting in asphalt stabilization. However, the study found that moisture damage weakened the water resistance of HBS cellulose-modified asphalt binder. Specifically, modifying asphalt with 8.62 wt% cellulose increased the Young modulus by 28.37%, bulk modulus by 39.77%, and shear modulus by 26.45%, demonstrating the overall improvement achieved with the combined effect of 8.62 wt% HBS cellulose-modified asphalt. These findings have significant implications for repurposing HBS as a solid waste material and enhancing the low-temperature crack resistance of asphalt binders.