Cellulose acetate (CA) fibers were electrospun on a mesh template to create specific surface and pore structures for membrane applications. The mesh template CA fiber mats were impregnated with cellulose nanocrystals at varying weight percentages. The membranes showed nanotextured surfaces and improved mechanical properties post impregnation. More importantly, the hydrophilicity of the original CA fibers was increased from a hydrophobic contact angle of 102°–0° thereby creating an anti-fouling membrane surface structure. The membranes showed rejection of 20–56% for particles of 0.5–2.0 μm, indicating potential of these membranes in rejecting microorganisms from water. Furthermore, high rejection of dyes (80–99%) by adsorption and potential application as highly functional affinity membranes was demonstrated. These membranes can therefore be utilized as all-cellulose, green, scalable and low cost high flux membranes (> 20,000 LMH) for water cleaning applications in food industry where microorganisms and charged contaminants are to be removed.

TEMPO (2,2,6,6-tetramethylpiperidine-1-oxylradical)-mediated oxidation nanofibers (TOCNF), as a biocompatible and bioactive material, have opened up a new application of nanocellulose for the removal of water contaminants. This development demands extremely sensitive and accurate methods to understand the surface interactions between water pollutants and TOCNF. In this report, we investigated the adsorption of metal ions on TOCNF surfaces using experimental techniques atthe nano and molecular scales with Cu(II) as the target pollutant in both aqueous and dry forms. Imaging with in situ atomic force microscopy (AFM), together with a study of the physiochemical properties of TOCNF caused by adsorption with Cu(II) in liquid, were conducted using the PeakForce Quantitative NanoMechanics (PF-QNM) mode at the nano scale. The average adhesion force between the tip and the target single TOCNF almost tripled after adsorption with Cu(II) from 50 pN to 140 pN. The stiffness of the TOCNF was also enhanced because the Cu(II) bound to the carboxylate groups and hardened the fiber. AFM topography, scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS) mapping and X-ray photoelectron spectroscopy (XPS) indicated that the TOCNF were covered by copper nanolayers and/or nanoparticles after adsorption. The changes in the molecular structure caused by the adsorption were demonstrated by Raman and attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR). This methodology will be of great assistance to gain qualitative and quantitative information on the adsorption process and interaction between charged entities in aqueous medium.

Barrier, mechanical and thermal properties of porous paper substrates dip-coated with nanocellulose (NC) were studied. Sorbitol plasticizer was used to improve the toughness, and citric acid cross-linker to improve the moisture stability of the coatings. In general, the addition of sorbitol increased the barrier properties, maximum strength and toughness as well as the thermal stability of the samples when compared to the non-modified NC coatings. The barrier properties significantly improved, especially for plasticized NC coating’s, where the oxygen permeability value was as low as 0.7 mL μm day⁻¹ m⁻² kPa⁻¹ at 49% RH and the water vapor permeability was reduced by 60%. Furthermore, we found that the cross-linked plasticized NC coating had a smoother surface (50% lower roughness) compared to non-modified ones. This study shows that the environmentally friendly additives sorbitol and citric acid had positive effects on NC coating properties, increasing its potential use in paper-based packaging applications.

In this study, the addition of hydroxyethyl cellulose (HEC) in cellulose nanofiber filaments is shown to improve the solvent-free processing and mechanical properties of these biobased fibers as well as their compatibility with epoxy. An aqueous dope of cellulose nanofiber (CNF) with HEC was spun and the resulting filaments cold-drawn. The HEC increased the wet strength of the dope allowing stable spinning of low concentrations of CNF. These lower concentrations promote nanofiber alignment which is further improved by cold-drawing. Alignment improves the modulus and strength and an increase of over 70% compared to the as-spun CNF only filaments was achieved. HEC also decreases hydrophilicity thus increasing slightly the interfacial shear strength of the filaments with epoxy resin. The result is continuous biobased fibers with improved epoxy compatibility that can be prepared in an upscalable and environmentally friendly way. Further optimization is expected to increase draw ratio and consequently mechanical properties.

The current work demonstrates an innovative approach to develop nanocellulose based membranes with high water permeability, mechanical stability and high functionality via (1) tailoring the composition of the support layer of sludge microfibers/cellulose nanofibers (CNF_SL) and (2) in situ TEMPO functionalization of the thin functional layer of cellulose nanocrystals (CNC_BE) to enhance the metal ion adsorption capacity. SEM studies showed a porous network structure of the cellulose support layer and a denser functional layer with CNC_BE embedded within gelatin matrix. AFM studies indicated the presence of a nanoscaled coating and increased roughness of membranes surface after TEMPO modification whereas FT-IR and conductometric titration confirmed the introduction of carboxyl groups upon TEMPO oxidation. The contact angle measurement results showed improved hydrophilic nature of membranes after in situ TEMPO functionalization. High networking potential of CNF_SL made the membrane support layer tighter with a concomitant decrease in the average pore size from 6.5 to 2.0 μm. The coating with CNC_BE further decreased the average pore size to 0.78 and 0.58 μm for S/CNC_BE and S–CNF_SL/CNC_BE, respectively. In parallel, a drastic decrease in water flux (8000 to 90 L MPa⁻¹ h⁻¹ m⁻²) after coating with CNC_BE was recorded but interestingly in situ functionalization of top CNC_BE layer did not affect water flux significantly. The increase in adsorption capacity of ≈1.3 and ≈1.2 fold was achieved for Cu(II) and Fe(II)/Fe(III), respectively after in situ TEMPO functionalization of membranes. Biodegradation study confirmed the stability of layered membranes in model wastewater and a complete degradation of membranes was recorded after 15 days in soil.

Fully bio-based three-dimensional porous scaffold for cartilage repair was prepared via freeze-drying where cellulose nanofibers, which were cytocompatible, were used as mechanical reinforcement (70-90 wt%) in a matrix of gelatin and chitosan (9:1) and crosslinked using genipin. Morphology studies showed that the scaffolds had interconnected pores with favorable pore diameters (< 250 μm) for cell growth. Compression modulus of the scaffolds (1-3 MPa) at room conditions was in the range for natural cartilage and decreased significantly (0.03-0.05 MPa) in phosphate buffered saline (PBS) at 37°C. The high PBS uptake shown by the scaffolds (< 3000 wt%) was attributed to liquid trapped in the pores during immersion in PBS. Furthermore, the scaffolds showed good cytocompatibility towards chondrocytes, which attached and proliferated properly. The scaffolds are considered to have potential in cartilage tissue engineering due to high porosity (≈ 95%) and good mechanical performance that promote cell attachment and extracellular matrix (ECM) production.

This paper deals with the effect of solution properties and nanoparticle surface chemistry on the spinnability of a chitosan/polyethylene oxide (PEO) with high concentration (50 wt%) of chitin and cellulose nanocrystals and the properties of the resultant nanocomposite fibers/fiber mats. Electrospinning dispersions with cellulose nanocrystals having sulphate surface groups showed poor spinnability compared to chitin nanocrystals with amide and amino groups. Chitin nanocrystal based dispersions showed good spinnability and continuous fiber formation whereas cellulose nanocrystal system showed discontinuous fibers and branching. The viscosity and surface tension are shown to impact this behavior, but conductivity did not. Poor spinnability observed for cellulose nanocrystal based fibers was attributed to the coagulation of negatively charged cellulose nanocrystals and positively charged chitosan. The study showed that the nanocrystal surface charge and interactions with the chitosan/PEO matrix have a significant impact on the spinnability of bionanocomposites.

Nanofiber mats or films are promising platforms that can offer unique opportunities in oromucosoal drug delivery. However, the conventional film forming technologies are unable to produce mats with unique internal microstructure and properties. Thus, the present study was aimed to develop electrospun nanofiber mats of a model drug -ondansetron hydrochloride (OND) for ultrafast drug release. Polyvinyl alcohol (PVA), a water soluble synthetic polymer was used in the preparation of nanofiber mats and casting film. The OND nanofiber mats and conventional films were prepared by electrospinning and casting methods, respectively. Different electrospinning process variables (feed rate, electric voltage and tip to collector distance) were investigated. Nanofiber mats and casted films were characterized using Scanning electron microscopy (SEM), Atomic force microscopy (AFM), Differential scanning calorimetry (DSC), Powder X-ray diffraction (PXRD), and Attenuated total reflection – Fourier transform infrared spectroscopy (ATR-FTIR). The folding endurance, drug content, wetting behaviour and disintegration properties and in-vitro drug release studies were also performed.The SEM and AFM had revealed that the nanofiber mats were formed with smooth uniform texture. Solid state studies indicated that the OND was in amorphous state and uniformly dispersed in PVA mats and a film. The electrospun nanofiber mat and casted film of OND showed sufficient mechanical properties. Wet sponge method suggested that OND nanofiber mats were simultaneously wetted and disintegrated within 10 s, which is ultrafast compared to casted films. The total amount of OND was released in 90 s (1.5 min) and 1800 s (30 min) from OND-PVA electrospun nanofiber mats and casted film, respectively. OND nanofiber mats can be promising alternatives to existing solid dosage forms for ultrafast release of drugs.