Because of their extraordinary electronic and mechanical properties, carbon nanotubes have great potential as materials for applications ranging from molecular electronics to ultrasensitive biosensors. Biological molecules interacting with carbon nanotubes provide them with specific chemical handles that would make several of these applications possible. Here we use phage display to identify peptides with selective affinity for carbon nanotubes. Binding specificity has been confirmed by demonstrating direct attachment of nanotubes to phage and free peptides immobilized on microspheres. Consensus binding sequences show a motif rich in histidine and tryptophan, at specific locations. Our analysis of peptide conformations shows that the binding sequence is flexible and folds into a structure matching the geometry of carbon nanotubes. The hydrophobic structure of the peptide chains suggests that they act as symmetric detergents.

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Lignin hollow nanospheres with a single hole were prepared through a straightforward self-assembly method, which included dissolving enzymatic hydrolysis lignin, a byproduct derived from biorefinery, in tetrahydrofuran and afterward dropping deionized water to the lignin/tetrahydrofuran solution. The formation mechanism and structural characteristics of the lignin hollow nanospheres were explored. The results indicated that the nanospheres exhibited hollow structure due to the effect of tetrahydrofuran on the self-assembly behavior. Hydrophobic outside surface and hydrophilic internal surface were formed via layer-by-layer self-assembly method from outside to inside based on π–π interactions. The chemical structure of lignin did not produce a significant change in the preparation process of lignin hollow nanospheres. With increasing of initial lignin concentration, the diameter of the nanospheres and the thickness of shell wall increased, while the diameter of the single hole, the surface area, and the pore volume of the nanospheres decreased. The surface area reached the maximum value (25.4 m2 g–1) at an initial lignin concentration of 0.5 mg/mL in setting concentration range. Increasing the stirring speed or dropping speed of water resulted in a decrease of the diameter of the hollow nanospheres. Moreover, an apparent change of the average diameter of the nanospheres was not observed after 15 days, and the nanosphere dispersions were stable at pH values between 3.5 and 12. The lignin hollow nanospheres with a single hole offer a novel route for a value-added utilization of lignin and would improve the biorefinery viability.

Natural fibers in micro and nano scales may be a potential alternative for man-made fibers because of the comparable mechanical properties to those of glass, carbon, and aramid fibers. Cellulose fibril and fibril aggregate are generally prepared by physical treatments, e.g., high-pressure homogenizer, or chemical treatments, e.g., acid hydrolysis. In this study, fibril aggregates were generated from a regenerated cellulose fiber by a novel mechanical treatment. The geometrical characteristics of the fibers and the fibril aggregates were investigated using scanning electron microscopy (SEM) and polarized light microscopy (PLM), and its crystallinity was investigated by wide angle X-ray diffraction (WAXD). The degree of fibrillation of the fibers was indirectly evaluated by water retention value (WRV). Nano-biocomposites reinforced with fibril aggregates were prepared by film casting and compression molding and evaluated by tensile test. The morphological characteristics of the nanocomposites were investigated with SEM and PLM. As reference, commercial microfibrillated cellulose was also used to reinforce biodegradable polymer.

Cellulose fibrils of microscale and nanoscale sizes have great strength and hence furnish the possibility of reinforcing polymers. Fibrils can be isolated from natural cellulose fibers by chemical or mechanical methods. However, the existing procedures either produce low yields or severely degrade the cellulose and, moreover, are not environment friendly or energy efficient. The purpose of this study was to develop a novel process that uses high-intensity ultrasonication (HIUS) to isolate fibrils from several cellulose resources. Six factors that may affect the efficiency of fibrillation, including power, temperature, time, concentration, size, and distance, have been considered and discussed. HIUS treatment can produce very strong mechanical oscillating power; therefore, the separation of cellulose fibrils from its biomass is possible by the action of hydrodynamic forces of the ultrasound. Water-retention value and volume change were used to evaluate and optimize the process parameters. The degree of fibrillation of the cellulose fibers treated by HIUS was significantly increased.

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