Cellulose nanomaterials (CNs) are of increasing interest due to their appealing inherent properties such as bio-degradability, high surface area, light weight, chirality and the ability to form effective hydrogen bonds across the cellulose chains or within other polymeric matrices. Extending CN self-assembly into multiphase polymer structures has led to useful end-results in a wide spectrum of products and countless innovative applications, for example, as reinforcing agent, emulsion stabilizer, barrier membrane and binder. In the current contribution, after a brief description of salient nanocellulose chemical structure features, its types and production methods, we move to recent advances in CN utilization as an ecofriendly binder in several disparate areas, namely formaldehyde-free hybrid composites and wood-based panels, papermaking/coating processes, and energy storage devices, as well as their potential applications in biomedical fields as a cost-effective and tissue-friendly binder for cartilage regeneration, wound healing and dental repair. The prospects of a wide range of hybrid materials that may be produced via nanocellulose is introduced in light of the unique behavior of cellulose once in nano dimensions. Furthermore, we implement some principles of colloidal and interfacial science to discuss the critical role of cellulose binding in the aforesaid fields. Even though the CN facets covered in this study by no means encompass the great amount of literature available, they may be regarded as the basis for future developments in the binder applications of these highly desirable materials.

The effect of three different types of cellulose nanofillers on the morphology, mechanical, and thermal properties of flexible polyurethane foam was studied. Cellulose nanocrystals (CNC), cellulose nanofibrils (CNF), and cellulose filaments (CelFil) were used as fillers at 0.1-0.8 wt% loading levels. The comparison of the results showed that smaller loading levels resulted in foams with better performance in almost all cases. In the next step, the properties of foams containing CNC, CNF, or CelFil at 0.025%-0.1% loading levels were compared with those made with inorganic nanofillers including nanosilica (nSi), reduced graphene oxide, and halloysite nanotubes (HNT). Among all the properties evaluated, the tensile modulus of the foams was improved up to 40% by adding HNT at 0.05 wt% loading level whereas the addition of CNF resulted in a 44% increase in the compressive modulus of the foams at 0.1 wt% loading level.

Cellulose nanofibrils (CNF) were spun into filaments directly from suspension without the aid of solvents. The influence of starting material properties and drying temperature on the properties of filaments produced from three different CNF suspensions was studied. Refiner-produced CNF was ground using a microgrinder at grinding times of 50 and 100 minutes. Filament spinning was performed using a syringe pump-heat gun setting at three drying temperatures of 210 • C, 320 • C and 430 • C. The structure of starting CNF materials was first evaluated using a combination of optical and atomic force microscopy (AFM) techniques. Surface free energy analysis and attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR) were used to study changes in hydrophobicity due to grinding. Morphology of the filaments was studied using SEM micrographs. The influence of different drying temperatures and grinding times on mechanical properties of the CNF filaments were further investigated through tensile tests and results were compared using statistical analysis .It was observed that drying temperature did not significantly influence the tensile properties of the filaments while cellulose nanofiber suspension type (grinding time) had a significant influence and improved mechanical properties. FTIR results confirmed an increase in crystallinity index and decrease in hydroxyl group availability due to grinding.

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