Cellulose Chains Research Articles

Molecular investigation of bamboo during stress relaxation using custom-built mechanical loading platform coupled with Raman spectroscopy

Bamboo holds significant potential as a substitute for plastics. Stress relaxation is a critical property during the fixation stage of plastic formation for bamboo products intended to replace plastic. However, research on this topic has been limited. In this study, a custom-built mechanical loading platform coupled with Raman spectroscopy was acquired during stress relaxation of bamboo under different humidity levels. Results reveal variations in stress relaxation patterns based on node position, radial location, and humidity, along with changes in cellulose molecules in response to these factors. Specifically, stress relaxation modulus in bamboo decreases from the outer to the inner part, increases in the presence of node structures, and decreases with increasing humidity. The shifts in Raman spectral bands exhibit significant changes in response to variations in stress and humidity. The elongation of cellulose chain bands at 1097 cm−1 in the Raman spectrum shows an increasing trend during stress relaxation, with larger band shifts observed at lower humidity. Simulations of cellulose molecular stretching show a stronger stress response at lower moisture content, with a maximum stress of 0.85 GPa for cellulose at 3.3 % moisture content, compared to 0.79 GPa at 7.8 % moisture content. These findings suggest a novel approach for the molecular investigation of materials during stress relaxation, which is crucial for the plasticity processing of bamboo.

Strong and ductile cellulose film improved by the in situ incorporation of a genetically engineered protein conjugated synthetic polymer during bacterial cellulose growth

Bacterial cellulose (BC) has been extensively applied to fabricate advanced biomaterials, although it remains challenging due to its poor toughness and water stability. Herein a genetically engineered protein-conjugated synthetic polymer is designed to improve BC film's strength and flexibility. Initially, the hybrid polymer is constructed by grafting Family 3 carbohydrate-binding modules (CBM3) to amphoteric polyacrylamide polymer (AmPAM), one of the paper industry's most widely used dry-strength agents. Then, the conjugated polymer is added to the culture medium of BC growth, enabling it to incorporate into the matrix of cellulose chains. The results show that the BC film modified by CBM3-AmPAM exhibits superior mechanical properties, registering 9.94 % in strain and 13.8 MJ/m3 in toughness, 12.1 and 8.0 folds over the sample with AmPAM addition only. Additionally, the BC film improved by CBM3-AmPAM has excellent gas resistance, thermal stability, and environmental endurance. The adsorption of CBM3-AmPAM on BC film revealed by quartz crystal microbalance with dissipation monitoring indicates that the adsorbed layer is thin and rigid, suggesting the strong interaction between the conjugated polymer and BC substrate. As a result of this reinforcing strategy, BC composites can be used in a wider range of applications.

Cell wall remodeling confers plant architecture with distinct wall structure in Nelumbo nucifera.

Lotus (Nelumbo nucifera G.) is a perennial aquatic horticultural plant with diverse architectures. Distinct plant architecture (PA) has certain attractive and practical qualities, but its genetic morphogenesis in lotus remains elusive. In this study, we employ genome-wide association analysis (GWAS) for the seven traits of petiole length (PLL), leaf length (LL), leaf width (LW), peduncle length (PLF), flower diameter (FD), petal length (PeL), and petal width (PeW) in 301 lotus accessions. A total of 90 loci are identified to associate with these traits across 4 years of trials. Meanwhile, we perform RNA sequencing (RNA-seq) to analyze the differential expression of the gene (DEG) transcripts between large and small PA (LPA and SPA) of lotus stems (peduncles and petioles). As a result, eight key candidate genes are identified that are all primarily involved in plant cell wall remodeling significantly associated with PA traits by integrating the results of DEGs and GWAS. To verify this result, we compare the cell wall compositions and structures of LPA versus SPA in representative lotus germplasms. Intriguingly, compared with the SPA lotus, the LPA varieties have higher content of cellulose and hemicellulose, but less filling substrates of pectin and lignin. Additionally, we verified longer cellulose chains and higher cellulose crystallinity with less interference in LPA varieties. Taken together, our study illustrates how plant cell wall remodeling affects PA in lotus, shedding light on the genetic architecture of this significant ornamental trait and offering a priceless genetic resource for future genomic-enabled breeding.

Molecular Dynamics Study of Hydrogen Bond Structure and Tensile Strength for Hydrated Amorphous Cellulose.

Molecular dynamics (MD) simulations were conducted to investigate the hydrogen-bond (H-bond) structure and its impact on the tensile strength of hydrated amorphous cellulose. The study identifies a stable intramolecular H-bond between the hydroxyl group at position 3 and the ether oxygen at position 5 (OH3···O5). Intermolecularly, the hydroxyl groups at positions 2 (OH2) and 6 (OH6) form stable H-bonds. Young's modulus, maximum tensile strength, and corresponding strain were calculated as functions of moisture content, while the H-bond network, water cluster formation, and cellulose chain orientation during tensile simulations were analyzed to elucidate mechanical properties. The substitution effect of cellulose on Young's modulus is also examined, revealing that the substitution of OH3 for a hydrophobic group minimally affects Young's modulus, but substitutions at OH2 and OH6 significantly reduce tensile strength due to their roles as key intermolecular H-bond donor sites.

Structural characteristics and biological evaluation of copper coating cotton material obtained by chemical reduction method

The article describes the preparation of new cotton materials obtained by chemical deposition of copper sulfide. This two-stage process consists of chelation of copper sulfate on cellulose chains of cotton (COT → COT-CuSO4) with subsequent precipitation of copper in the form of copper sulfide (COT-CuSO4 → COT-CuS) using sodium sulfide. The obtained COT-CuS composites were characterized physicobiologically. Thus, the structural characteristic of the Cotton-CuS material was determined by microscopy analysis (SEM), Atomic Absorption Spectrometry with Flame Excitation (FAAS), specific surface area and total pore volume analysis (BET). The copper functionalized cotton fabric was subjected to microbial activity tests against colonies of Gram-negative (Escherichia coli) and Gram-positive ( Staphylococcus aureus) bacteria and Chaetomium globosum, Aspergillus niger fungal molds species. Biochemical evaluation includes hematological tests of activated partial thromboplastin time (aPTT) and prothrombin time (PT). The substantial antimicrobial properties of the newly synthesized COT-CuS material with the lack of influence on blood coagulation processes offer prospects of a potential use as applications as an antibacterial/antifungal material.

Enhancing the Mechanical Properties of Regenerated Cellulose through High-Temperature Pre-Gelation

This paper investigates the effects of pre-gelation on cellulose dissolved in LiCl/DMAc solutions to enhance the properties of regenerated cellulose materials. This study focuses on characterizing the crystallinity, molecular orientation, and mechanical performance of cellulose fibers and hydrogels prepared with and without pre-gelation treatment. X-ray diffraction (XRD) analysis reveals that crystallinity improvement from 55% in untreated fibers to 59% in fibers pre-gelled for 3 and 7 days, indicating a more ordered arrangement of cellulose chains post-regeneration. Additionally, XRD patterns show improved chain alignment in pre-gelled fibers, as indicated by reduced full width at half the maximum of Azimuthal scans. Mechanical testing demonstrates a 30% increase in tensile strength and a doubling of the compression modulus for pre-gelled fibers compared to untreated fibers. These findings underscore the role of pre-gelation in optimizing cellulose material properties for applications ranging from advanced textiles to biomaterials and sustainable packaging. Future research directions include further exploration of the structural and functional benefits of pre-gelation in cellulose processing and its broader implications in material science and engineering.

Cellulose Fiber with Enhanced Mechanical Properties: The Role of Co-Solvents in Gel-like NMMO System.

Cellulose has garnered attention in the textile industry, but it exhibits limitations in applications that require high strength and modulus. In this study, regenerated cellulose fiber with enhanced mechanical properties was fabricated from a gel-like N-methylmorpholine N-oxide (NMMO)-cellulose solution by modulating the intermolecular interaction and conformation of the cellulose chains. To control the interaction, two types of co-solvents (dimethyl acetamide (DMAc) and dimethyl formamide (DMF)) were added to the cellulose solutions at varying concentrations (10, 20, and 30 wt%). Rheological analysis showed that the co-solvents reduced the solution viscosity by weakening intermolecular interactions. The calculated distance parameter (Ra) in Hansen space confirmed that the co-solvent disrupted intermolecular hydrogen bonding within cellulose chains. The solutions were spun into fiber via a simple wet spinning process and were characterized by X-ray diffraction (XRD) and universal testing machine (UTM). The addition of co-solvent led to an increased crystallinity index (C.I.) owing to the extended cellulose chains. The modulus of the resulting fiber was increased when the co-solvent concentration was 10 wt%, regardless of the co-solvent type. This study demonstrates the potential for enhancing the mechanical properties of cellulose-based products by modulating the conformation and interaction of cellulose chains through the addition of co-solvent.

Bioinspired surface silicification of cellulose-mediated PVDF membranes for significantly enhancing superhydrophilicity and anti-oil adhesion toward ultrafast oil/water emulsion separation

Cellulose is a widely used hydrophilic material due to its rich hydrophilic hydroxyl groups. However, the presence of its lipophilic segment will affect the antifouling performance. Finding strategies to improve this problem has attracted considerable attention. In this work, a layer of silica was applied to a cellulose-deposited polyvinylidene fluoride membrane through a straightforward in-situ bionic silicification process of tetraethyl orthosilicate. The contact angle and oil droplet contact test proved that the high-hydrophilicity and underwater superoleophobicity of the silicified membranes were significantly enhanced. The surface structure and composition were analyzed by scanning electron microscopy, Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. The results of show that this improvement was mainly attributed to the presence of silicon hydroxyl groups, buried cellulose chains, and micro-nanostructures composed of cellulose and silica. The stable silica coating also provided protection for the polymeric membrane against degradation after water washing for 24 h, ultrasonic treatment (40 KHZ) for 10 min or exposure to different pH levels (pH=1, 4, 9 and 12) and saturated sodium chloride solution for 24 h. Furthermore, the silicified membrane showed outstanding oil adhesion resistance and permeation flux, enabling effective purification of different oil-in-water emulsions that were stabilized by emulsifiers. Notably, the membrane achieved a high oil removal rate (> 99.4 %) of various emulsions (toluene-in-water, cyclohexane-in-water, tetrachloroethane-in-water, soybean oil-in-water, toluene-in-salt solution, toluene-in-acid solution and toluene-in-alkaline solution emulsions). In particular, for toluene-in-water emulsions (oil droplets in the emulsion ranged from 58.77 nm to 615.1 nm), a significantly enhanced permeation flux (4777 L·m−2·h−1·bar−1) was obtained at 0.8 bar pressure. Even after multiple cycles of separation, the flux was higher than that of the unsilicified membrane. Overall, this approach is mild, simple, efficient, and easily scalable, making it an ideal method for producing superhydrophilic coatings with substantial application potential.

Highly functionalized all-cellulose nanocomposites via bacteria-enabled in-situ modifications

Bacterial cellulose (BC) is an appealing class of nanoscale biopolymers with immense potential for sustainable development across food, energy, and health sectors. However, facile, green approaches to convert BC into functional, value-added materials remain limited. Here, novel BC nanocomposites are developed by incorporating highly functional amorphous cellulose chains, called “hairs”. It is shown how in-situ modifications via integrating hairy nanocrystalline cellulose (HNCC) into cellulose-synthesizing Komagataeibacter medellinensis media enable all-cellulose nanocomposites with diverse functional groups. As a result, sterically stabilized HNCC (SNCC) with neutral aldehyde, electrosterically stabilized HNCC (ENCC) with carboxyl and bifunctional HNCC (BNCC) with both aldehyde-carboxyl groups yield hairy BC/SNCC (aldehyde ∼ 0.9 mmol g−1), BC/ENCC (carboxyl ∼ 1.5 mmol g-1) and BC/BNCC (aldehyde ∼ 0.8 mmol g-1 and carboxyl ∼ 1.1 mmol g-1) nanocomposites, respectively. These nanocomposites, characterized by finely tuned chemistry and architecture, offer versatile sustainable platforms. Anionic BC/ENCC and BC/BNCC are loaded with the antibacterial ɛ-poly-L-lysine (PLL) to explore drug adsorption isotherms, release kinetics, and underlying mechanisms. The antibacterial efficacy of hairy nanocomposites is quantified, followed by a biocompatibility assessment with human bone marrow stromal cells (hBMSC). This work lays the foundation for BC conversion to highly functional advanced nanocomposites for a wide range of applications.

Dynamic borate ester bond reinforced hydroxyethyl cellulose/corn starch crosslinked film for simple recycling and regeneration

Endowing biodegradable plastics with easy recyclability can reduce competition with food resources and further enhance their environmental friendliness. In this work, 4-carboxyphenylboronic acid was grafted onto the side chains of hydroxyethyl cellulose and compounded with inexpensive cornstarch. Upon the introduction of tannic acid, stable and reversible borate ester bond rapidly formed, yielding composite biodegradable plastic films with outstanding mechanical properties and facile recyclability. The formation of a dynamic cross-linked network mitigates the aggregation of gelatinized starch molecules, enhancing the flexibility and durability of the crosslinked film. Testing revealed that while maintaining high tensile strength, the elongation at break of the crosslinked film increased by 952.86 %. The static water contact angle was improved from 32.74° to 78.82°, with a change of <5° within 1 min, demonstrating enhanced water resistance. Excellent antioxidant and thermal stability were also characterized, the crosslinked film can be easily dissolved by heating in water at pH = 6.5 and reshaped in water at pH = 7.2. After five times of regeneration, the tensile strength loss was as low as 5.68 %. This eco-friendly and efficient recycling process is promising during green chemistry.

High aspect ratio cellulose nanofibrils with low crystallinity for strong and tough films

Cellulose nanofibril (CNF) films with both high strength and high toughness are attractive for applications in energy, packaging, and flexible electronics. However, simultaneously achieving these mechanical properties remains a significant challenge. Herein, a multiscale structural optimization strategy is proposed to prepare high aspect ratio CNFs with reduced crystallinity for strong and tough films. Carboxymethylation coupled with mild mechanical disintegration is employed to modulate the multiscale structure of CNFs. The as-prepared CNFs feature an aspect ratio of >800 and a crystallinity of <60 %. The film prepared using CNFs with a high aspect ratio (~1100) and reduced crystallinity (~54 %) exhibits a tensile strength of 229.9 ± 9.9 MPa and toughness of 22.2 ± 1.4 MJ/m3. The underlying mechanism for balancing these mechanical properties is unveiled. The high aspect ratio of the CNFs facilitates the transfer and distribution of local stress, thus endowing the corresponding film with high strength and toughness. Moreover, the low crystallinity of the CNFs permits the movement of the cellulose chains in the amorphous regions, thereby dissipating energy and finally increasing the film toughness. This work introduces an innovative and straightforward method for producing strong and tough CNF films, paving the way for their broader applications.

Cellulose-based fluorescent chemosensor with controllable sensitivity for Fe3+ detection

Polymer-based sensors, particularly those derived from renewable polymers, are gaining attention for their superior properties compared to organic small molecules. However, their complex preparation and poor, uncontrollable sensitivity have hindered further development. Herein, cellulose-based polymer photoluminescence (PL) chemosensors were fabricated using a straightforward and adjustable strategy. Specifically, water-soluble cellulose acetoacetate (CAA) was used as the substance for the in-situ synthesis of 1,4-dihydropyridine (DHPs) fluorescent rings on cellulose chains via a catalyst-free, room-temperature Hantzsch reaction. Benefiting from the synergetic through-space conjugation of DHPs rings and semi-rigid cellulose chains with heteroatoms, the sensors exhibit bright and stable PL properties. Based on this performance, the cellulose-based sensor excels in the specific recognition of Fe3+ in aqueous systems, showing exceptional selectivity, stability, and anti-interference performance due to the synergy between the inner filter effect (IFE) and intramolecular charge transfer (ICT). Theoretical calculations confirm the role of the extended π-conjugated structure at the DHPs-4 position in modulating the sensor sensitivity, achieving a low limit of detection (LOD) of 0.48 μM. Furthermore, the versatility of the Hantzsch reaction shows the potential of this strategy for developing a new generation of biomass-based polymer portable sensors for real-time and on-site detection.

Preparation of bacterial cellulose/acrylic acid-based pH-responsive smart dressings by graft copolymerization method

Conventional wound dressings used in trauma treatment have a single function and insufficient adaptability to the wound environment, making it difficult to meet the complex demands of the healing process. Stimuli-responsive hydrogels can respond specifically to the particular environment of the wound area and realize on-demand responsive release by loading active substances, which can effectively promote wound healing. In this paper, BC/PAA-pH responsive hydrogels (BPPRHs) were prepared by graft copolymerization of acrylic acid (AA) to the end of the molecular chain of bacterial cellulose (BC) network structure. Antibacterial pH-responsive ‘smart’ dressings were prepared by loading curcumin (Cur) onto the hydrogels. Surface morphology, chemical groups, crystallinity, rheological, and mechanical properties of BPPRHs were analyzed by different characterization methods. The drug release behavior under different physiological conditions and bacteriostatic properties of BPPRH-Cur dressings were also investigated. The results of structural characterization and performance studies show that the hydrogel has a three-dimensional mesh structure and can respond to wound pH in a ‘smart’ drug release capacity. The drug release behavior of the BPPRH-Cur dressings under different environmental conditions conformed to the logistic and Weibull kinetic models. BPPRH-Cur displayed good antimicrobial activity against common pathogens of wound infections such as E. coli, S. aureus, and P. aeruginosa by destroying the cell membrane and lysing the bacterial cells. This study lays the foundation for the development of new pharmaceutical dressings with positive health, economic and social benefits.

Study of the effect of bleaching agents on the crystalline index of cellulose-based materials derived from corn husk by CP/MAS 13C NMR and FT-IR spectroscopies

This work proposes an evaluation of the Crystalline Index (CrI) in function of the bleaching process employed during cellulose extraction from corn husk, for further characterization using CP/MAS 13C NMR, XRD, and FT-IR. In that sense, CrI values were calculated by FT-IR and the bands associated with the crystalline and amorphous regions were observed at 1424 cm−1 and 896 cm−1, respectively. Similarly, the signals due to ordered (89.1 ppm) and disordered (84.2 ppm) cellulose chains were detected by solid-state 13C NMR, while the Segal equation was only used for comparison purposes. Additionally, PCA studies showed consistent results attributed to the crystalline region in cellulose domains analyzed by both, FT-IR and solid-state 13C NMR. The results revealed the coexistence of cellulose I/cellulose II and its effect on CrI, as well as the incomplete mercerization process, in some cases non-cellulosic residues can cause an overestimation of CrI. Additionally, the thermal stability and the glass transition temperature were determined by TGA/DTA and DSC analyses. Finally, a partially fibrillated-network morphology with a diameter of 20.47 ± 2.77 μm was observed in cellulose bleached with peracetic acid, whereas organosolv method provides flexible and clean microfibrils with diameter sizes between 10 and 9 μm.

Impact of lignocellulosic nanofiber source on the performance of polylactic acid

AbstractComposites based on polylactic acid (PLA) were developed, using lignocellulosic nanofibers (LCNF) dispersed in polyethylene glycol (PEG). To evaluate the impact of LCNF sources, suspensions were prepared from different pulps, including only cellulose; other with cellulose and hemicellulose; and cellulose, hemicellulose, and lignin. The PLA/PEG ratio was 80/20, with LCNF concentrations of 1.25%, 2.5%, and 3.75% (w/w) relative to the PLA/PEG weight. The best results were achieved with 2.5% (w/w) of LCNF containing a blend of cellulose and hemicellulose, showing a 26% increase in tensile strength and 102% in Young's modulus compared with the PLA/PEG matrix. The hemicellulose in LCNF acts as a physical barrier between cellulose chains, demonstrating a lower tendency for agglomeration and greater compatibility with PEG and PLA, as evidenced by decreased zeta potential due to the adsorption of PEG and shifts in the CO peak in the FTIR spectra. At 3.75 LCNF concentration, micrometer‐sized fibers were observed in SEM images, impacting the mechanical properties of the composites. Thermograms show no phase separation, and the change in crystallinity due to the addition of nanofibers has minimal influence on mechanical properties. These findings highlight the importance of selecting appropriate lignocellulosic nanoparticles for improved material performance.

Antiscaling Pickering Emulsions Enabled by Amphiphilic Hairy Cellulose Nanocrystals.

Nucleation and growth of sparingly soluble salts, referred to as scaling, has posed substantial challenges in industrial processes that deal with multiphase flows, including enhanced oil recovery (EOR). During crude oil extraction/recovery, seawater is injected into oil reservoirs and yields water-in-oil (W/O) emulsions that may undergo calcium carbonate (CaCO3) scaling. Common antiscaling macromolecules and nanoparticles have adverse environmental impacts and/or are limited to functioning only in single-phase aqueous media. Here, we develop a novel antiscaling cellulose-based nanoparticle that enables scale-resistant Pickering emulsions. Cellulose fibrils are rationally nanoengineered to yield amphiphilic hairy cellulose nanocrystals (AmHCNC), bearing hydrophilic dicarboxylate groups and hydrophobic alkyl chains on disordered cellulose chains (hairs) protruding from nanocrystal ends. The unique chemical and structural properties of AmHCNC render them the first dual functional antiscaling and emulsion stabilizing nanoparticle. AmHCNC stabilize W/O Pickering emulsions at a concentration of 1.00 wt % for 1 week while inhibiting CaCO3 scale formation up to 70% by mass at a supersaturation degree of ∼101 compared with the synthetic surfactant Span 80. To the best of our knowledge, this study presents the first biopolymer-based solution for the long-lasting scaling challenge in multiphase media, which may set the stage for developing sustainable scale-resistant multiphase flows in a broad spectrum of industrial sectors.

High-barrier, flexible, hydrophobic, and biodegradable cellulose-based films prepared by ascorbic acid regeneration and low temperature plasma technologies

Regenerated cellulose (RC) films are considered a sustainable packaging material that can replace non-degradable petroleum-based plastics. However, their susceptibility to water vapor and oxygen can limit their effectiveness in protecting products. This study introduces a novel approach for enhancing RC films to create durable, flexible, hydrophobic, high-barrier, and biodegradable packaging materials. By exploring the impact of ascorbic acid coagulation bath treatment and plasma-enhanced chemical vapor deposition (PECVD) on the properties of RC films, we found that the coagulation bath treatment facilitated the organized reconfiguration of cellulose chains, while PECVD applied a dense SiOx coating on the film surface. The results demonstrated a significant enhancement in water vapor and oxygen barrier properties of the composite film, almost reaching the level of commercial barrier films. Moreover, the composite film displayed exceptional biodegradability, fully degrading in soil within 35 days. Additionally, it showcased impressive mechanical strength, hydrophobic characteristics, and freshness preservation, positioning it as a valuable option for bio-based high-barrier packaging applications.

Cellulose-based colorimetric/ratiometric fluorescence sensor for visual detecting amines and anti-counterfeiting

Many amines with high toxicity always cause a serious threat to the ecological environment and human health; thus, their detection is important. Herein, a dual-mode colorimetric and ratiometric fluorescent sensor based on cellulose for detecting amines has been constructed by a new strategy. This sensor is made of a “negative response” indicator (Lum-MDI-CA) and a “positive response” indicator (perylene tetracarboxylic acid, PTCA). Lum-MDI-CA was obtained by attaching luminol onto cellulose chains, which emitted blue fluorescence and was quenched upon contact with amines. A possible mechanism of fluorescence quenching phenomenon is proposed by the intramolecular charge transfer (ICT) of Lum-MDI-CA. Subsequently, by simply mixing Lum-MDI-CA with PTCA, a dual-mode fluorescence sensor was designed for visual detection and classification of amines. When adding ammonia (NH3), morpholine (MOR), benzylamine (BNZ), diethylamine (DEA), and triethylamine (TEA), respectively, the dual-mode sensor showed visible different color changes under both UV light and daylight. In addition, owing to the excellent processibility and formability of cellulose acetate backbone, the prepared sensor can be easily processed into different material forms, including inks, coatings, films, and fibers, which still exhibit excellent fluorescence emission. Such sensors based on cellulose fluorescent materials are of great value in anti-counterfeiting and information encryption.

Production of lignin-containing nanocellulose from six types of unpretreated lignocellulosic biomass by a one-step process

Lignin-containing nanocellulose (LCN) shows great potential in the fabrication of high performance bio-based materials, and suitable raw materials may achieve the production of LCN in a more economical approach. Therefore, in this study, the morphology, chemical and supramolecular structure of six types of lignocellulosic biomass (Broussonetia papyrifera bark, moso bamboo, rattan, balsa wood, poplar wood and fir wood) were analyzed for the production of LCN by using pure oxalic acid dihydrate (OAD). The results revealed that BPBs is a natural available cellulose-rich materials with extremely high cellulose content, low lignin content, and loosely connected cellulose chains. Compared with the other five types of lignocellulosic biomass materials, the hydrolysis of BPBs without any pretreatments by using OAD produced higher yield of LCN with much more uniform size distribution and smaller size. LCN from BPBs had higher crystallinity and thermal stability than that from the other five lignocellulosic biomass. The finding in this study indicated that Broussonetia papyrifera bark without any pretreatment was a favored material for high yield production of LCN compared with the other woody materials, which provided an economically realizable method on the efficient and high yield production of LCN from unpretreated BPBs by using OAD hydrolysis.

High tensile regenerated cellulose fibers via cyclic freeze-thawing enabled dissolution in phosphoric acid for textile-to-textile recycling of waste cotton fabrics

Recycling of waste cotton fabrics (WCFs) is a desirable solution to address the problems brought up by fast fashion, but it remains challenging due to inherent limitations in preparing stable and spinnable dopes by dissolving high molecular weight cellulose efficiently and cost effectively. Herein, we show that despite the prevailing concerns of cellulose degradation via glycosidic hydrolysis when dissolved in acids, fast and non-destructive direct dissolution of WCFs in aqueous phosphoric acid (a.q. PA) could be realized using a cyclic freeze-thawing procedure, which combined with subsequent adjustment of degree of polymerization (DP) and degassing yielded stable and spinnable dopes. Regenerated cellulose fibers (RCFs) with favorable tensile strength (414.2 ± 14.3 MPa) and flexibility (15.4 ± 1.5 %) could be obtained by carefully adjusting the coagulation conditions to induce oriented and compact packing of the cellulose chains. The method was shown to be conveniently extended to dissolve reactively dyed WCFs, showing great potential as a cheap and green alternative to heavily explored ionic liquids (ILs) and N-methylmorpholine-N-oxide (NMMO)-based systems for textile-to-textile recycling of WCFs.