Cellulose Fibers Research Articles

In Situ Synthesis of Metal-Organic Frameworks on Sulfonated Cellulose Nanofibrils

The intrinsic fragility and inferior processibility of metal-organic frameworks (MOFs) particles often restrict their functional application despite their high surface area and porous structure. We investigated the feasibility of sulfonated cellulose nanofibrils (SCNF) as a biopolymer and template to hybridize MOFs. SCNF was synthesized through periodate oxidation followed by bisulfite sulfonation and characterized using solution-state NMR spectra. The sulfonate groups increased electronegativity and enhanced the dispersibility of the cellulose fibers. More importantly, the negatively charged sulfonates could be manipulated as anchors for metal ions to initiate the in situ growth of MOFs along the surface of cellulose fibers. We have achieved the synthesis of three types of SCNF/MOF hybrids, namely, SCNF/ZIF-8, SCNF/ZIF-67, and SCNF/HKUST-1. These hybrids can be formed as free-standing aerogels, exhibiting remarkably high surface areas and flexibility for applications. The assessment of the adsorptive efficiency of the SCNF/ZIF-8 hybrid indicates that the hybrid material exhibited a notably higher adsorption capacity for methylene blue versus the SCNF control. DFT computational calculation provides further insights into the underlying adsorption mechanisms, revealing that the sulfonates on the SCNF and the nitrogen atoms in the ZIF-8 ligands primarily contributed to the affinity for methylene blue. SCNF offers a versatile and robust biopolymer substrate for templating a wide array of MOFs with promising applications as adsorbents and beyond.

Properties, Production, and Recycling of Regenerated Cellulose Fibers: Special Medical Applications

Regenerated cellulose fibers are a highly adaptable biomaterial with numerous medical applications owing to their inherent biocompatibility, biodegradability, and robust mechanical properties. In the domain of wound care, regenerated cellulose fibers facilitate a moist environment conducive to healing, minimize infection risk, and adapt to wound topographies, making it ideal for different types of dressings. In tissue engineering, cellulose scaffolds provide a matrix for cell attachment and proliferation, supporting the development of artificial skin, cartilage, and other tissues. Furthermore, regenerated cellulose fibers, used as absorbable sutures, degrade within the body, eliminating the need for removal and proving advantageous for internal suturing. The medical textile industry relies heavily on regenerated cellulose fibers because of their unique properties that make them suitable for various applications, including wound care, surgical garments, and diagnostic materials. Regenerated cellulose fibers are produced by dissolving cellulose from natural sources and reconstituting it into fiber form, which can be customized for specific medical uses. This paper will explore the various types, properties, and applications of regenerated cellulose fibers in medical contexts, alongside an examination of its manufacturing processes and technologies, as well as associated challenges.

Comparative Analysis of Mechanical and Morphological Properties of Cordenka and Ramie Fiber-Reinforced Polypropylene Composites

The depletion of conventional materials and their adverse environmental impacts have prompted a shift toward sustainable alternatives in composite materials engineering. In pursuit of this objective, this study investigated the mechanical properties of polypropylene matrix composites reinforced with Cordenka, an artificial cellulose fiber, and compared them to those reinforced with ramie, a natural cellulose fiber. Continuous strand composites were developed using the Multi-Pin-assisted Resin Infiltration (M-PaRI) process. The strands were subsequently sectioned into 15 mm lengths and injection-molded into dumbbell and strip specimens for mechanical characterization. The results showed that 20 wt% Cordenka/PP composites exhibited a tensile strength of 68.7 MPa, 2.04 times higher than neat PP and 1.66 times greater than the 20 wt% ramie/PP composites. Impact testing further demonstrated that Cordenka/PP composites absorbed 2 to 2.5 times more impact energy than ramie/PP composites, regardless of the presence of notches. Fiber length analysis indicated that Cordenka fibers maintained their length beyond the critical fiber length, allowing for efficient stress transfer and acting as a more effective reinforcement compared to ramie fibers, which were below this threshold. Consequently, the Cordenka/PP composites exhibited significantly enhanced mechanical performance. Scanning electron microscopy (SEM) analysis revealed fewer fiber pullouts in ramie-reinforced composites, suggesting superior interfacial adhesion to the PP matrix, although it did not translate to higher mechanical properties. These findings underscore the potential of Cordenka as a sustainable alternative to synthetic, non-biodegradable fibers in PP composites, providing improved mechanical properties and promising prospects for advanced composite applications.

Rheology of Cellulosic Microfiber Suspensions Under Oscillatory and Rotational Shear for Biocomposite Applications

This study investigates the rheological behavior of cellulose microfiber suspensions derived from kahili ginger stems (Hedychium gardnerianum), an invasive species, in two adhesive matrices: a commercial water-based adhesive (Coplaseal®) and a casein-based adhesive made from non-food-grade milk, referred to as K and S samples, respectively. Rheological analyses were performed using oscillatory and rotational shear tests conducted at 25 °C, 50 °C, and 75 °C to assess the materials’ viscoelastic properties more comprehensively. Oscillatory tests across a frequency range of 1–100 rad/s assessed the storage modulus (G′) and loss modulus (G″), while rotational shear tests evaluated apparent viscosity and shear stress across shear rates from 0.1 to 1000 s−1. Fiber-free samples consistently showed lower moduli than fiber-containing samples at all frequencies. The incorporation of fibers increased the dynamic moduli in both K and S samples, with a quasi-plateau observed at lower frequencies, suggesting solid-like behavior. This trend was consistent in all tested temperatures. As frequencies increased, the fiber network was disrupted, transitioning the samples to fluid-like behavior, with a marked increase in G′ and G″. This transition was more pronounced in K samples, especially above 10 rad/s at 25 °C and 50 °C, but less evident at 75 °C. This shift from solid-like to fluid-like behavior reflects the transition from percolation effects at low frequencies to matrix-dominated responses at high frequencies. In contrast, S samples displayed a wider frequency range for the quasi-plateau, with less pronounced moduli changes at higher frequencies. At 75 °C, the moduli of fiber-containing and fiber-free S samples nearly converged at higher frequencies, indicating similar effects of the fiber and matrix components. Both fiber-reinforced and non-reinforced suspensions exhibited pseudoplastic (shear-thinning) behavior. Fiber-containing samples exhibited higher initial viscosity, with K samples displaying greater differences between fiber-reinforced and non-reinforced systems compared to S samples, where the gap was narrower. Interestingly, S samples exhibited overall higher viscosity than K samples, implying a reduced influence of fibers on the viscosity in the S matrix. This preliminary study highlights the complex interactions between cellulosic fiber networks, adhesive matrices, and rheological conditions. The findings provide a foundation for optimizing the development of sustainable biocomposites, particularly in applications requiring precise tuning of rheological properties.

Development and Performance of ZnO/MoS2 Gas Sensors for NO2 Monitoring and Protection in Library Environments

The presence of harmful oxidizing gases accelerates the oxidation of cellulose fibers in paper, resulting in reduced strength and fading ink. Therefore, the development of highly sensitive NO2 gas sensors for monitoring and protecting books holds significant practical value. In this manuscript, ZnO/MoS2 composites were synthesized using sodium molybdate and thiourea as raw materials through a hydrothermal method. The morphology and microstructure were characterized by X-ray diffraction analysis (XRD), energy dispersive spectroscopy (EDS), field emission scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The ZnO/MoS2 composite exhibited a flower-like structure, with ZnO nanoparticles uniformly attached to the surface of MoS2, demonstrating advantages such as high specific surface area and good uniformity. The gas sensitivity of the ZnO/MoS2 nanocomposites reached its peak at 260 °C, with a sensitivity value around 3.5, which represents an improvement compared to pure ZnO, while also enhancing sensitivity. The resistance of the ZnO/MoS2 gas sensor remained relatively stable in air, exhibiting short response times during transitions between air and NO2 environments while consistently returning to a stable state. In addition to increasing adsorption capacity and improving light utilization efficiency, the formation of hetero-junctions at the ZnO-MoS2 interface creates an internal electric field that effectively promotes the rapid separation of photo-generated charge carriers within ZnO, thereby extending carrier lifetime.

Improvement of Adsorption Capacity by Refined Encapsulating Method of Activated Carbon into the Hollow-Type Spherical Bacterial Cellulose Gels for Oral Absorbent

To reduce the risk of adsorption of granular activated carbon (AC) in the gastrointestinal tract, we successfully prepared a hollow-type spherical bacterial cellulose gel encapsulated with AC (ACEG) and evaluated its pH tolerance and adsorption capacity. The bacterial cellulose gel membrane of ACEG features a three-dimensional mesh structure of cellulose fibers, allowing the selective permeation of substances based on their size. In this study, the preparation method of ACEGs was investigated, and the indole saturation adsorption capacity of the obtained gel was measured. We modified the gel culture nucleus gel from calcium alginate gel to agar gel, facilitating the encapsulation of previously challenging particles. The new preparation method used sodium hydroxide solution for sterilization and dissolution to remove the debris of Komagataeibacter xylinus, which was feared to remain in the bacterial cellulose membrane. This treatment was also confirmed to have no effect on the adsorption capacity of the AC powder. Therefore, this new preparation method is expected not only to improve the performance of ACEGs but also to be applied to a wide range of adsorbent-encapsulated hollow-type bacterial cellulose gels.

Genetic characterization and mapping of the shell-strength trait in peanut.

Shell strength is an important trait in peanuts that impacts shell breakage and yield. Despite its significance, the genetic basis of shell strength in peanuts remains largely unknown, and the current methods for rating this trait are qualitative and subjective. This study aimed to investigate the genetics of shell strength using a segregating recombinant-inbred-line (RIL) population derived from the hard-shelled cultivar 'Hanoch' and the soft-shelled cultivar 'Harari'. Initially, a quantitative method was developed using a texture analyzer, focusing on the proximal part of isolated shells with a P/5 punching probe. This method revealed significant differences between Hanoch and Harari. Shell strength was then measured in 235 RILs across two distinct environments, revealing a normal distribution with some RILs exhibiting shell strength values beyond those of the parental lines, indicating transgressive segregation. Analysis of variance indicated significant effects for the RILs, with no effects of block or year, and a broad-sense heritability estimate of 0.675, indicating a substantial genetic component. Using an existing genetic map, we identified three QTLs for shell strength, with one major QTL (qSSB02) explaining 18.7% of the phenotypic variation. The allelic status of qSSB02 corresponded significantly with cultivar designation for in-shell or shelled types over four decades of Israeli peanut breeding. Physical and compositional analyses revealed that Hanoch has a higher shell density than Harari, rather than any difference in shell thickness, and is associated with increased levels of lignin, cellulose, and crude fiber. These findings provide valuable insights into the genetic and compositional factors that influence shell strength in peanut, laying a foundation for marker-assisted selection in breeding programs focused on improving pod hardness in peanuts.

Investigating the Routes to Produce Cellulose Fibers from Agro-Waste: An Upcycling Process

The agriculture and agri-food sectors produce substantial amounts of plant-based waste. This waste presents an identifiable research opportunity to develop methods for effectively eliminating and managing it in order to promote zero-waste and circular economies. Plant-based waste and by-products are acknowledged as valuable sources of bioactive compounds, including cellulose fibers. Direct application of these fibers in non-food sectors such as textiles can reduce the environmental impact of secondary raw materials. This review aims to provide an overview of novel concepts and modern technologies for efficiently utilizing plant-based waste and by-products from the agricultural and agro-industrial sectors to extract fibers for a variety of final applications, including the fashion industry. Two major routes are identified to produce cellulose fibers: the extraction and purification of natural cellulose fibers and the extraction and purification of cellulose pulp that is further processed into manmade cellulosic fibers. Scalability of experimental results at the laboratory or pilot level is a major barrier, so it is critical to develop closed-loop processes, apply standardization protocols, and conduct life cycle assessments and techno-economic analyses to facilitate large-scale implementation.

Ultralight Poly(vinyl alcohol)/Cattail Fiber Cellulose Aerogels as Green and Recyclable Organic Liquid Captors

Ultralight Poly(vinyl alcohol)/Cattail Fiber Cellulose Aerogels as Green and Recyclable Organic Liquid Captors

Environmental modification of cellulose fibers for reducing dye diffusion rate by anionic polyacrylamide

Reactive dyeing is the primary method for coloring cellulose fibers due to its vibrant colors, various hues, excellent colorfastness, and cost-effectiveness. However, this process consumes a large amount of water and chemicals, leading to significant environmental concerns due to the wastewater. Non-aqueous media/less water dyeing has emerged as a cleaner alternative, showing promising results in dyeing cotton fibers with reactive dyes. Nevertheless, the rapid adsorption rate of dyes can impact the evenness of dyeing. This study explores the use of anionic polyacrylamide (APAM) in the modification bath to reduce dye adsorption rate and enhance dye desorption during cellulose fibers dyeing. Fourier transform infrared spectroscopy (FT-IR) and field-emission scanning electron microscope (FSEM) analysis revealed effective interaction between APAM and cellulose fibers. Thermal gravimetric analysis (TGA), X-ray diffraction (XRD), and breaking strength tests indicated minimal impact on the thermal stability and physical properties of cellulose fibers with APAM modification. Zeta potential testing demonstrated that APAM modification reduced the surface potential of cellulose fibers and increased their negative charge. The adsorption rate of reactive dye decreased with APAM modification, while dye fixation, washing, and rubbing fastness remained largely unaffected. Adsorption isotherm results supported the weakening of the affinity between dyes and fibers after APAM treatment. Furthermore, the electrostatic potentials of fibers decreased after APAM modification. Compared to salt-free dyeing in non-aqueous media dyeing systems, anionic polymer modification not only improves the level dyeing performance of cotton fiber and reduces 0.9% in dyeing costs, but also increases production efficiency.

Rheo-impedance behavior of cellulose nanofibers produced by mechanical processing

AbstractCNFs are one of the renewable and the sustainable resources with low environmental impact and have various characteristics such as increased strength and weight reduction when added to resins. Since CNFs are one of the new materials that can fulfill the goals of the Sustainable Development Goals (hereafter abbreviated as SDGs), many researchers have been studying the nano-fibrillation of wood fibers. From the viewpoint of SDGs, it is necessary to avoid using a large amount of chemical agents and consuming a large amount of energy for the production of CNFs. To realize these requirements, it is important to find a way to industrially utilize CNFs containing insufficiently nanosized fibers, and for these purposes, it is essential to evaluate the physical properties of these CNFs from multiple perspectives. Cellulose fibers are intrinsically insulating materials, but how their electrochemical properties are changed by nano-fibrillization has been little studied. Therefore, we decided to clarify the relationship between the size of CNFs and the electrochemical impedance properties of the CNF suspensions containing un-fibrillated fibers, which were prepared by a wet refinement system. The fiber diameter remained constant as the number of mechanical treatments (hereafter referred to as the “number of collisions”) increased. On the other hand, the cumulative medium volume diameter, D50, defined as the apparent fiber length (hereafter referred to as the “fiber length”, in microns), significantly decreases with the increasing number of collisions. The rheo-impedance |Z| of the CNF suspension remained nearly constant in the intermediate frequency range of 103–106 Hz, even if the internal structure of the system was deformed by the increasing shear rate. This means that the electrochemical properties of the CNFs are independent of the changes in the macroscopic aggregation structure. Furthermore, the internal resistance R1 calculated from the impedance |Z| characteristics (Nyquist plot) became decreased with the increasing number of collisions, indicating a proportional relationship between the resistance R1 and the CNF fiber length, D50. This suggests that R1 related to the resistance caused by the electrolyte in the suspensions or the protons dissociated by the hydration of the hydroxyl groups of the cellulose molecule as they move across the gaps between the microfibrils. Based on these results, it appears that the electrochemical properties of the CNF suspensions are independent of the changes in the macroscopic aggregation structure and simply depend on the fiber length, in other words, the electrochemical properties are a useful method for indirectly evaluating the fiber length of the CNFs.

Histochemical and gene expression changes in Cannabis sativa hypocotyls exposed to increasing concentrations of cadmium and zinc

Hemp (Cannabis sativa L.) is a versatile crop that produces cellulosic bast fibres used in textiles and biocomposites. Is also finds use in phytoremediation, being a good candidate for the cultivation on marginal lands, such as those contaminated by heavy metals (HMs). HMs like cadmium (Cd) and zinc (Zn) are known to affect plant growth and impair the biosynthesis of cellulose and lignin at the cell wall level. Since cellulose is the major component in the gelatinous layer of bast fibres, HMs can impact the structure of hemp fibres and, consequently, their mechanical properties. This study investigates how varying concentrations of Cd and Zn in the soil affect the bast fibres of hemp plantlets. The chosen model is the hypocotyl, as it is ideal for studying bast fibre development: it exhibits a temporal separation between the elongation and thickening phases within a short period of approximately three weeks. C. sativa plantlets were grown for 20 days, and the hypocotyls sampled to perform histochemical observations, gene expression analysis, as well as to quantify biomass yield and Cd/Zn accumulation. Hemp plantlets grown in soils with the three highest Zn concentrations were smaller than the control group, whereas no decrease in size was observed under elevated Cd concentrations. However, at the highest Cd concentration, the root system exhibited enhanced development, accompanied by a significant increase in dry weight across all the concentrations tested. The quantification of Cd and Zn showed that the roots were the main organs accumulating HMs. Cd at the two highest concentrations decreased significantly the lumen area of bast fibres and increased their cell wall thickness. Zn decreased significantly the lumen area, but it did not impact the thickness of the cell wall at the highest concentration. Cd also increased the number of secondary fibres. Immunohistochemistry highlighted a different pattern of crystalline cellulose distribution with a signal that was less homogeneous in the presence of Cd and Zn. Gene expression analysis revealed changes in transcripts encoding cellulose synthases, fasciclin-like arabinogalactan proteins, class III peroxidases. The results obtained shed light on the molecular response and bast fibre histological changes occurring in young hemp plants exposed to Cd and Zn.

Immobilization of urea on beads based on OPEFB cellulose-alginate via blending to fabricate sustained release fertilizer

Transforming oil palm empty fruit bunches (OPEFB) waste into value-added cellulose as a reinforcement agent for eco-friendly slow-release fertilizer (SRF) composites is a strategy to achieve clean and sustainable production. OPEFB cellulose was isolated by alkalization (10 % w/v NaOH) for 1 h and bleaching (30 % v/v H2O2) for 1.5 h. The treatment increased the cellulose content to 80.88 %, reduced the non-cellulosic component, and improved the fiber crystallinity to 58.40 %. The hydrogel composite was cross-linked by blending urea in an OPEFB cellulose fiber (w/w) (0 %, 0.5 %, and 1 %) and sodium alginate (3 % w/w). Then, the wet beads were freeze-dried to fabricate SRF composites. Each material was evenly dispersed in the matrix, had a porous structure, and could bind total nitrogen up to 20.0 %, confirmed by the Kjeldahl method. Adding cellulose increased crystallinity (significant at 1 % w/w cellulose), decreased bulky density (significant at 0.5 % and 1 % w/w cellulose), increased swelling capacity (significant at 0.5 % w/w cellulose), and water-retention capacity. Reinforced composite with 0.5 % (w/w) cellulose released nitrogen into the soil (Fickian diffusion) following the Higuchi model (R2 = 0.957) with K = 0.0394 and equilibrium at around t1/2 = 1.8 h. Changing SRF composite properties are likely related to the porous structure loaded with urea crystals.

Protective fibrous structures based on cellulose fibers functionalized with metal oxide nanoparticles by electrospinning and electrospray deposition

Protective fibrous structures based on cellulose fibers functionalized with metal oxide nanoparticles by electrospinning and electrospray deposition

Wood meet MOFs: Facile, green, and highly selective adsorbent for textile wastewater

Owing to their unique physicochemical features, ionic liquids (ILs) are extensively utilized to dissolve cellulose for the preparation of regenerated cellulose fibers (RCFs) in the textile industry. However, Cu2+ is introduced during the cellulose dissolution process and gradually accumulates, seriously affecting the RCF performance and IL recovery. Herein, to achieve an efficient and selective adsorption of Cu2+ from ILs aqueous solutions, a facile and green method based on the in situ growth of zeolitic imidazolate framework-67 in wood hydrogels (ZIF-67@WH) is presented. The morphology, functional groups, crystallinity, thermal stability, and pore structure of the resulting ZIF-67@WH were investigated using various characterization techniques, and the adsorption selectivity, adsorption thermodynamics, adsorption kinetics, and recoverability were examined in depth by performing batch experiments. The ZIF-67@WH exhibits high adsorption selectivity for Cu2+ and ILs with adsorption ratios of 92.8 % and 2.2 %, respectively. The selective adsorption mechanism was elucidated by means of FT-IR, XPS, DFT, and MD. As the key for the selective adsorption, the N site in ZIF-67 dramatically promotes the coordination with Cu2+, while the adsorption for ILs mainly occurs via hydrogen bonding and van der Waals interactions with adsorption energies of –80.61 and –35.33 kcal/mol, respectively. The results demonstrate that this approach constitutes a feasible technique for the efficient separation of Cu2+ and ILs in the textile industry.

Optimising wound healing: the role of gelling fibre technology and antimicrobial silver nanoparticles.

Gelling-fibre dressings have been found to be a rapid and effective tool for exudate management. Suprasorb Liquacel Pro is a soft, conformable non-woven dressing made from sodium carboxymethyl cellulose and strengthening cellulose fibres. When it comes into contact with wound exudate or blood, the absorbent dressing forms a gel, creating a moist wound environment. Cell debris and bacteria in the exudate are retained inside the fibre dressing and removed during the dressing change. The high vertical absorption of exudate into the fibre dressing protects the wound environment and the wound edge, thus supporting the healing process. Suprasorb Liquacel Ag has additional antimicrobial abilities with the inclusion of nanosilver technology, shown to be effective in killing bacteria and managing bioburden.

Upcycling Industrial Biomass Wastes Into Aerogels Using Zinc Chloride Salt Hydrates

AbstractEnd‐of‐life paper products, including food packages and rejected fibers from the paper industry, are unrecyclable biomass wastes and thus generally landfilled or incinerated. One of the major obstacles to their recycling is the existence of impurities besides cellulose fiber in the biomass wastes. In this study, a fabrication method is investigated to upcycle biomass wastes directly into high‐performance aerogels without separation of impurities. Surprisingly, this study observes that residual impurities participate in cross‐linking reactions for the aerogel formation. In this study, zinc chloride salt hydrate is applied to convert biomass wastes to aerogel via a dissolution‐regeneration process. The fabricated aerogels exhibited high water absorption capacity (15 times its weight), as well as comparable mechanical strength and thermal insulation performance to the reported cellulose aerogels. In addition, the impurities (i.e., calcium‐based inorganic salt) assisted in the cross‐linking of the cellulose network for the aerogel formation. The scanning electron microscopy (SEM) image of the aerogel generated from the rejected fibers showed a honeycomb inner structure. The rejected fiber aerogels also demonstrated a high compressive modulus of 51 MPa and a low thermal conductivity of 0.029 W m−1 K−1. The results for water absorption and thermal insulation suggest excellent potential across various application domains.

Nanocrystalline cellulose from Calophyllum inophyllum shells waste by adjusting organic acid hydrolysis and optimization of reaction parameters using response surface methodology

Biodiesel production from Calophyllum inophyllum oil in Indonesia produces significant biomass waste, including seed shells. This study explores the conversion of the seed shell of Calophyllum inophyllum into nanocrystalline cellulose (NCC) via consecutive alkalization, bleaching and hydrolysis using various organic acids. Scanning electron microscopy (SEM) analysis showed a reduction in the diameter of cellulose fibers from 21.7 μm to 9.6 μm after alkalinization and bleaching. The hydrolysis process using several organic acids was optimized to produce thermally stable nanocellulose while maintaining its crystallinity. The diameter of the resulting nanofibrous cellulose was 20.53 nm for citric acid, 21.69 nm for maleic acid, and 22.06 nm for formic acid hydrolysis. In particular, lactic acid-derived NCC (NCC-LA) showed the highest crystallinity of 64.22 % with an average diameter of ~13.69 nm. Optimization of hydrolysis parameters using Response Surface Methodology (RSM) suggested 74.79 % crystallinity could be achieved with 6.01 M lactic acid following 3.46 h of hydrolysis at 91.12 °C.

Influence of Chemical, Morphological, Spectroscopic and Calorimetric Properties of Agroindustrial Cellulose Wastes on Drainage Behavior in Stone Mastic Asphalt Mixtures.

New asphalt mixtures have been improved by using fibers (polypropylene, polyester, asbestos, carbon, glass, nylon, lignin, coconut, sisal, recycled rubber, PET, wood, bamboo, and cellulose), reducing the temperature and compaction energy for their collocation, minimizing the impact on the environment, increasing the tenacity and resistance to cracking of hot mix asphalt (HMA), preventing asphalt drainage in a Stone Mastic Asphalt (SMA). Hence, this paper aims to evaluate the influence of the chemical (lignin content, ash, viscosity, degree of polymerization, and elemental analysis), morphological (SEM), spectroscopic (FTIR-ATR and XRD), and calorimetric (ATG and DSC) properties of celluloses from bagasse Agave tequilana Weber var. Azul (ABP), corrugated paperboard (CPB) and commercial cellulose fiber (CC) as Schellenberg drainage (D) inhibitors of the SMA. The ABP was obtained through a chemical process by alkaline cooking, while CPB by a mechanical refining process. The chemical, morphological, spectroscopic, and calorimetric properties were similar among the analyzed celluloses, but CPB and ABP cellulose are excellent alternatives to CC cellulose for inhibiting drainage. However, CPB is the most effective at low concentrations. This is attributed to its morphology, which includes roughness, waviness, filament length, orientation, and diameter, as well as its lignin content and crystallinity.

Rapid surface acetylation of cellulosic materials at room temperature by immersion method

Regulating the surface hydrophobicity of cellulosic materials via surface acetylation can greatly extend their applications. However, most of the existing surface acetylation methods for cellulosic materials are time-consuming and costly. Herein a simple but practical immersion method for the rapid surface acetylation of cellulose materials was reported, which involved soaking cellulosic materials in alkaline aqueous solution followed by immersed them in vinyl acetate. Results showed that simply wetting the surface of cellulosic materials with aqueous alkaline solutions can satisfy their surface acetylation requirement, and the consumption of esterifying agent can be significantly reduced. The immersion method can rapidly improve the surface properties of the cellulosic materials at room temperature within minutes and which is highly attractive to the surface acetylation of cellulose fibers. The moisture regain of the viscose filament obviously decreased after surface acetylation. When the surface acetylated viscose fiber was used as cigarette filter, the total particulate matter in the filtered cigarette smoke significantly reduced from 11.03 mg/cigarette to 6.03 mg/cigarette. The products are promising alternatives to the existing cigarette filters.